CA1300064C - Process for enhancing the cetane number and color of diesel fuel - Google Patents
Process for enhancing the cetane number and color of diesel fuelInfo
- Publication number
- CA1300064C CA1300064C CA000558370A CA558370A CA1300064C CA 1300064 C CA1300064 C CA 1300064C CA 000558370 A CA000558370 A CA 000558370A CA 558370 A CA558370 A CA 558370A CA 1300064 C CA1300064 C CA 1300064C
- Authority
- CA
- Canada
- Prior art keywords
- diesel oil
- diesel
- treating agent
- blended
- treated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A process for enhancement of the cetane number of a diesel fuel which in one embodiment comprises:
(1) treating a diesel oil with a nitrogenous treating agent in a nitrogen amount, equivalent on a 100% nitric acid basis, to about 10 weight percent or less of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated diesel oil of step (3) with an untreated diesel oil to produce a blended diesel fuel such that the added nitrogen content in the blended diesel fuel is (a) about 300 ppm or less of nitrogen added when the diesel oil treated in step (1) is obtained from virgin diesel oil stock; or (b) about 450 ppm or less of nitrogen added when the diesel oil treated in step (1) is obtained from hydrotreated diesel oil stock.
A process for enhancement of the cetane number of a diesel fuel which in one embodiment comprises:
(1) treating a diesel oil with a nitrogenous treating agent in a nitrogen amount, equivalent on a 100% nitric acid basis, to about 10 weight percent or less of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated diesel oil of step (3) with an untreated diesel oil to produce a blended diesel fuel such that the added nitrogen content in the blended diesel fuel is (a) about 300 ppm or less of nitrogen added when the diesel oil treated in step (1) is obtained from virgin diesel oil stock; or (b) about 450 ppm or less of nitrogen added when the diesel oil treated in step (1) is obtained from hydrotreated diesel oil stock.
Description
~01)~6~
PROCFSS FOR ~N~ANCING T~ CET~NE
NUMBER ~ND COLOR OE DI~SEL FUEL
EIELD OE THE INVENTION
This invention provides a process for upgrading a diesel oil by treatment of a diesel oil with a nitroge-nous treating agent to increase the cetane rating and improve the color of the treated oil, and blending the treated oil with an untreated diesel oil to obtain in the diesel fuel blend a cetane increase, good color, good stability and useful levels of Ramsbottom carbon.
More particularly, in an embodiment of the present process, the extent of nitrogen addition to the treated diesel oil used in the diesel fuel blend and the blend ratio of treated to untreated diesel oil are controlled in one embodiment to insure that the concentration o added nitrogen in the final blended diesel fuel product does not exceed about 300 ppm in the case of virgin diesel oil stocks, or about 450 ppm in the case of hydrotreated diesel oil stocks.
; BACKGROUND OF THE INVENTION
It has long been known that the cetane number of diesel oils can be improved either by adding a nitrogen-containing fuel additive, or by treatment with a nitrogenous oxidizing agent. Oils in the diesel 13~1~0~4 boiling point range having the proper physical charac-teristics such as pour point, cloud point, viscosity and volatility can be obtained by nitrating the diesel fraction in order to increase the cetane number.
However, it is well known that the nitration of such oils tends to increase the Ramsbottom carbon content and to decrease the stability of the fuels by forming an insoluble sediment. The insoluble sediment produces a haze and eventually a deposit while the fuels are in storage. While many attempts to eliminate the disadvantage of poor stability characteristics have been made and solvent extraction, including alkali scrubbing, has been employed to improve stability, conventional solvent extraction has proven unsatisfac-tory to provide acceptable stability in the case of nitrogen-treated fuels.
Solvent extraction with certain organic solvents, such as those described in United $tates patents 4,643,820 and 4,746,420, is effective to improve stability and reduce Ramsbottom carbon content, but a ma~or portion of the cost of upgrading diesel oil by this method is incurred in the solvent extraction process. A method of improving the cetane rating of substandard diesel oils that does not 1~
~3~ 64 require an expensive solvent extraction step to meet diesel fuel product specifications for stability and Ram~bottom carbon is particularly desirable.
It is known to enhance the cetane number of diesel oil using oxidative processes. Regarcling the use of nitration to improve the cetane number of diesel oil~, British Patent No. 491,648 teache~ contacting a diesel oil with a nitrating agent in order to increase its ce-tane number. The disclosure in British Pa-tent No~ 4gl,648 is that the nitrated oil can be used alone or in a blend with untreated diesel oil. Extraction with solvents including acetone, methyl and ethyl alcohols, ethylene dichloride and aniline is described for obtaining concentrates of nitrated petroleum components. However, by contacting a diesel oil with a nitrating agent, stability is decreased and Ra~sbottom carbon is increased, and these de~iciencies are combined with poor process yields when the product is extracted using the solvents disclo~ed. While recognizing the problem of sedimentation and poor stability, this British Patent contains no suggestion as to how these problems can be reduced or eliminated.
U.S. Patent No. 39135,680 discloses oxidation of a sour petroleum fraction with nitrogen dioxide followed by washing with water and alkali, to desulfurize diesel 06~
oils and improve cetane. The disclosure is that the product obtained, however, tends to have an objectionable color resulting from the nitrogen dioxide treatment, and subsequent sulfuric acid treatment, vacuum distillation or clay treating is considered essen-tial to completely remove materials formed during oxidation. Unfortunately, this reduces or eliminates the increase in cetane number. Due to its high Ramsbottom carbon content, the product of this process forms substan-tial coke in the still upon distillation.
A proces~ is described in U.S. Patent 3,164,546 for producing diesel fuels having improved cetane number and odor, by treating the oil with nitrogen dioxide, washing with aqueous alkali and/or solvent extraction, followed by a water wash. Solvents disclosed as suitable for the solvent extraction step are nitromethane, dimethylformamide, pyridine, acetonitrile, glycolonitrile, ethylene glycol, ethanolamine and phenol. No reference is made, however, to the important stability and Ramsbottom carbon content specifications, which are by far the most difficult product specifications to meet for a diesel fuel product when employing nitrogenous treating agents. Furthermore, extraction reduces yields of product.
.
~3~00~
U.S. Patent No. 2,333,817 discloses oxidation of diesel oils by nitrogenous compounds followed by hexane dilution and filtering to improve cetane and prevent sediment formation. Such a product does not pass present~day indu~try standards for stability ~although haze formation is reduced) and it does not meet Ramsbottom carbon ~pecifications. From the exemplification it appears this techni~ue is only applicable to cycle oils.
These methods have generally apparently employed nitration or an oxidation treatment for cetane improvement of diesel oils, but lt is also ~nown that the cetane number of diesel oils can be increased by adding various nitrated hydrocarbon derivatives to the oils, including amyl nitrate, octyl nitrate, and the nitrate ester "dopes" disclosed in British Patent No.
491,648. Other nitrogen-containing additives for improving cetane are disclosed in U.S. Patent No.
4,398,505. Use of these derivatives is generally disadvantageous since they are expensi~e and must be separately prepared, handled and ~tored.
U.S. Patent No. 2,184,440 relates to methods of increasing the cetane number of blended diesel fuels by blending diesel fuels from different sources, one of which is a high sulfur crude, and treating the blended 130006~L
fuel with sodium plumbite and a large excess of elemental sulfur. Alternatively, a distillate fuel stock can be treated with ~odium plumbite and an excess amount o elemental sulfur over that reguired to sweeten the 6tock, and distilled to obtain a sweetened condensate, with the bottoms being further reduced and added to an untreated diesel fuel to increase the cetane number of the blend. The reduced bottoms amounting to about 1 to 6% of the original distillate fuel stock are added in amounts of about 0.5 to 5% to diesel fuels to raise their cetane number, e.g., by 2 to 19 over untreated diesel fuel.
U.S. Patent No. 2,104,919 provides a means to achieve a stabilized fuel by blending straight-run and cracked stocks. The disclosure of this patent states that typically fuel oils produced by blending straight-run components and cracked residues have a tendency to form a carbonaceous sludge on storage, and the precipitation of sludge in such fuels containing 10 to 80% heavy cracked residues is inhibited by mildly oxidizing the straight-run component before blending, e.g., by blowing air at 250-400C therethrough for l/2 to 12 hours.
U.S. Patent No. 2,317,96~ disclose~ a die~el fuel containing substantial portions of chemically combined ~30~t~6~
reactive oxygen through treatment with air, oxygen or an oxyyen carrying gas, to produce by partial oxidation a petroleum fuel having a volatility greater than that of kerosene and relatively free from asphaltic and resinous components and from large proportions of aromatics, to an "oxygen factor" of 800 to 1450 by air blowing, removal of acids produced by oxidation, and blending with a diesel fuel to produce a diesel fuel blend having increased cetane. Blends of 2.5% oxidized oil to 97.5% by volume sulfur dioxide-treated petroleum distillate and of 20% by volume of oxidized oil to 80%
by volume of a clean gas oil distillate are disclosed.
U.S. Patent No. 2,365,220 discloses a method similar to that o U.S. Patent 2,317,968. The disclosure is of the preparation of a diesel fuel, in which a diesel fuel of predominately paraffinic character is oxidized using air, oxygen or an oxygen carrying gas to produce an oil having an "oxygen factor" of higher than 5, acidic reaction products are rsmcved, and the resulting oxidized stock is blended with from 2/5 to 20 time~ its volume of a clean diesel petroleum hydrocarbon distillate.
U.S. Patent No. 2,521,698 discloses that the fuels produced by the methods of U.S. Patent Nos. 2,317,968 and 2,365,220 are unstable and corrosive, and that the ~31DOl)~
stability and corrosiveness of such cetane-enhanced diesel fuels can be improved with a loss of about 25%
of cetane enhancement, by subjecting the oxidized diesel fuel to acid treatment with a strong acid, such as sulfuric or nitric acid, in a concentration of at least 0.1 pound per gallon of ox$dized stock, followed by alkali wash and blending of the treated oxidized stock with diesel fuel. A concentrated oxygenated cetane-improving additive is also disclosed, prepared from the bottoms of the distilled oxidized diesel stock.
U.S. Patent 4,280,818 discloses oxidizing a hydrocarbon oil with aqueous nitric acid in a weight ratio of about 1:0.1 to 1:10 of hydrocarbon to acid and separating the aqueous phase from the oxidized hydrocarbon phase. The disclosure is that the oxidized hydrocarbon phase can be extracted and the product obtained blended with a polar solvent to produce a fuel mixture.
U.S. Patent No. 3,284,342 discloses oxidation of residue using a number of oxidants including nitrogen oxides, followed by a thermal treatment to reduce the sulfur content of the residue, in which both s-teps can be promoted with catalysts. When applied to diesel oil, this process produces substantial carbonaceous 01~6~
deposits in the thermal treating still, and is unsatisfactory for commercial use.
U.S. Patent 3,135,680 discloses a process for refining petroleum fractions in the diesel oil boiling range to produce diesel fuel with enhanced cetane number and odor by treating the fractions with nitrogen dioxide followed by a clay treatment to remove odor.
A process of deodorizing and desulfurizing light petroleum distillatss by treatment with nitrogen dioxide ollowed by alkali wash and water wash is disclosed in U.S. Patent No. 3,267,027. This process i~ unsuitable for producing diesel fuels of acceptable stability and Ramsbottom carbon content.
U.S. Patent No. 3,244,618 discloses a process for sweetening petroleum hydrocarbons by treating the hydrocarbon fraction with molecular oxygen in the presence of a catalytic amount of a nitrogen oxide.
Application of this process to diesel fuel results in a product with inferior cetane enhancement.
U.S. Patent No. 2,004,849 discloses the use of an oxidant, hydrogen peroxide, in combination with sulfuric acid to effect sulfur removal from hydrocarbons, without substantial loss of aromatics.
However, this process is ineffective for improving the cetane of di~sel fuel.
1~0(1 ~4 Processes for treating petroleum 6tocks by oxidation ~ollowed by solvent extraction have been described for various purposes.
For example, a process for producing a fuel composition by oxidizing a hydrocarbon oil with aqueous nitric acid, followed by extraction with acetone, methyl ethyl ketone, cyclohexanone, methanol, ethanol, normal propanol, isopropanol, ethyl acetate, tetrahydrofuran, dioxane, or a combination of an alcohol and a ketone, an alcohol and water, a ketone and water or a combination o alcohols is disclosed in U.S. Patent No. 4,280,~18.
Although the oxidation/extraction methods described above have met with some success in improving petroleum diesel fueLs, the known approaches toward oxidation to remove a portion of the original sulfur content as gaseous sulfur oxide~, and to convert a portion of the original sulfur content into sulfoxides and/or sulfones followed by extraction with appropriate solvents to achieve a desired low sulfur raffinate have not completely eliminated problems of in~tability and unacceptable Ramsbottom carbon for diesel fuels, and have the disadvantage of an expensive solvent extraction step, resulting in low yields.
13006)6A
The methods described above when applied to petroleum stocks for use as diesel fuels basically have the disadvantages that (a) oxidative desulfurization methods involving nitrogenous oxidizing agents often result in increased gum and sedimentation, and reduce the stability of the fuels produced, (b) the oxida-tively treated fuel~ are not useful as diesel fuel blendstocks due to poor stability and high Ramsbottom carbon content, and (c) solvent extraction, while effective to im~roVe stability and Ramsbottom carbon content, is expen~ive and of low product yield~ in comparison to oxidative treatment alone where the oxidized product alone can be blended to improve diesel fuels.
While many conventional methods of improving diesel cetane number by oxidation with nitrogenous oxidizing agents exist, they are generally inadequate to meet other product specifications. Particularly, diesel fuels produced by nitrogeneous oxidation and solvent extraction can in svme cases meet sulfur and cetane requirements for fuels, but are unsatisfactory with respect to the important specifications of stability and Ramsbottom carbon content. Processes employing sulfuric acid or clay in conjunction with nitrogeneous oxidizing agents are inefective to retain ~O~O~i4 a high cetane rating when pxacticed to control Ramsbottom carbon and stability. Distillative methods are commercially unfeasible due to the presence of substantial carbonaceous deposits in the still, and when thermal trea-ting is applied to diesel fuel to reduce sulfur content of the residue, this process also produces substarltial carbonaceous deposits in the thermal treating still. Often acceptable color levels in the product, particularly after storage, are not achievable.
Apart from the failure o conventional oxida-tive cetane enhancement methods to provide diesel fuels of sufficient stability and Ramsbottom carbon content, these methods, like the oxidative desulfurization methods, employ solvents which result in poor yields?
re~uiring unacceptably high solvent-to-oil ratios.
Alternatively, the sol~ent~ used in some methods reduce or entirely eliminate the advantage of cetane enhancement obtained by oxidation.
While certain of the patents cited above refer to oxidation of diesel stocks to improve cetane~ and the use o ~uch oxidatively enhanced stocks in blends with unoxidized diesel fuels, these patents fail to recognize the importance of limiting the nitrogen content of the final blend to achieve acceptable ~L3~00Ç;g~
stability or Ramsbottom carbon content in the final blend. Furthermore, there is no appreciation of the remarkable increase of cekane in the treated por-tion and in the final blend when nitrogen treatment and blending are controlled according to the present process. Finally, thare is no recognition o~ the further benefits of selected alkaline wash agents in imparting improved color stability while retaining the foregoing attributes.
SUMMARY OF T~E INVENTION
An object of the invention i8 to provide a process for enhancing the cetane number o a diesel fuel.
Another object of the invention is to provide a process for increasing the cetane number and improving the color of a diesel fuel e.g., preventing the development of color in the blend product over development of color in the blend product not subjected to the proces~ of this invention comprising treating the diesel oil with a nitrogenous treating agent, separating unreacted nitrogenous treating agent, treating the diesel oil with an inorganic alkali, and then blending the treated diesel oil with an untreated diesel oil in specific proportions to produce a blended diesel fuel having an unexpectedly increased cetane number and with marked improvement in the color of the ~30006~L
blended diesel fuel, compared to blending the treated oil without use of an alkali treating agent.
A further object of this lnvention is to provide a blended diesel fuel with improved cetane number and appropriate stability and Ramsbottom carbon.
An even further object of this invention is to provide a blended diesel fuel in which the amount of additive which might be added to enhance even ~urther the stability o~ the blended diesel fuel is minimized.
Also, an object of thi~ invention is to provide a process for producing a blended diesel fuel having good storage stability and color along with useful levels of Ramsbottom carbon.
When the alkali used for treatment is ln an aqueous solution form, a further object of the invention is to minimize the chemical oxygen demand in treatment of the spent alkali wash water for release in the environment or for recycle/reuse.
In one embodiment of this invention, this invention provide3 a process for the enhancement of the cetane number of and improvement in color developed on storage of a diesel fuel comprising:
(1) treating a diesel oil with a nitrogenou~
treating agent in a nitrogen amount, equivalent on a 100% nitric acid basis, to ~..3~
about 10 weight percent or less of the diesel oil feed;
PROCFSS FOR ~N~ANCING T~ CET~NE
NUMBER ~ND COLOR OE DI~SEL FUEL
EIELD OE THE INVENTION
This invention provides a process for upgrading a diesel oil by treatment of a diesel oil with a nitroge-nous treating agent to increase the cetane rating and improve the color of the treated oil, and blending the treated oil with an untreated diesel oil to obtain in the diesel fuel blend a cetane increase, good color, good stability and useful levels of Ramsbottom carbon.
More particularly, in an embodiment of the present process, the extent of nitrogen addition to the treated diesel oil used in the diesel fuel blend and the blend ratio of treated to untreated diesel oil are controlled in one embodiment to insure that the concentration o added nitrogen in the final blended diesel fuel product does not exceed about 300 ppm in the case of virgin diesel oil stocks, or about 450 ppm in the case of hydrotreated diesel oil stocks.
; BACKGROUND OF THE INVENTION
It has long been known that the cetane number of diesel oils can be improved either by adding a nitrogen-containing fuel additive, or by treatment with a nitrogenous oxidizing agent. Oils in the diesel 13~1~0~4 boiling point range having the proper physical charac-teristics such as pour point, cloud point, viscosity and volatility can be obtained by nitrating the diesel fraction in order to increase the cetane number.
However, it is well known that the nitration of such oils tends to increase the Ramsbottom carbon content and to decrease the stability of the fuels by forming an insoluble sediment. The insoluble sediment produces a haze and eventually a deposit while the fuels are in storage. While many attempts to eliminate the disadvantage of poor stability characteristics have been made and solvent extraction, including alkali scrubbing, has been employed to improve stability, conventional solvent extraction has proven unsatisfac-tory to provide acceptable stability in the case of nitrogen-treated fuels.
Solvent extraction with certain organic solvents, such as those described in United $tates patents 4,643,820 and 4,746,420, is effective to improve stability and reduce Ramsbottom carbon content, but a ma~or portion of the cost of upgrading diesel oil by this method is incurred in the solvent extraction process. A method of improving the cetane rating of substandard diesel oils that does not 1~
~3~ 64 require an expensive solvent extraction step to meet diesel fuel product specifications for stability and Ram~bottom carbon is particularly desirable.
It is known to enhance the cetane number of diesel oil using oxidative processes. Regarcling the use of nitration to improve the cetane number of diesel oil~, British Patent No. 491,648 teache~ contacting a diesel oil with a nitrating agent in order to increase its ce-tane number. The disclosure in British Pa-tent No~ 4gl,648 is that the nitrated oil can be used alone or in a blend with untreated diesel oil. Extraction with solvents including acetone, methyl and ethyl alcohols, ethylene dichloride and aniline is described for obtaining concentrates of nitrated petroleum components. However, by contacting a diesel oil with a nitrating agent, stability is decreased and Ra~sbottom carbon is increased, and these de~iciencies are combined with poor process yields when the product is extracted using the solvents disclo~ed. While recognizing the problem of sedimentation and poor stability, this British Patent contains no suggestion as to how these problems can be reduced or eliminated.
U.S. Patent No. 39135,680 discloses oxidation of a sour petroleum fraction with nitrogen dioxide followed by washing with water and alkali, to desulfurize diesel 06~
oils and improve cetane. The disclosure is that the product obtained, however, tends to have an objectionable color resulting from the nitrogen dioxide treatment, and subsequent sulfuric acid treatment, vacuum distillation or clay treating is considered essen-tial to completely remove materials formed during oxidation. Unfortunately, this reduces or eliminates the increase in cetane number. Due to its high Ramsbottom carbon content, the product of this process forms substan-tial coke in the still upon distillation.
A proces~ is described in U.S. Patent 3,164,546 for producing diesel fuels having improved cetane number and odor, by treating the oil with nitrogen dioxide, washing with aqueous alkali and/or solvent extraction, followed by a water wash. Solvents disclosed as suitable for the solvent extraction step are nitromethane, dimethylformamide, pyridine, acetonitrile, glycolonitrile, ethylene glycol, ethanolamine and phenol. No reference is made, however, to the important stability and Ramsbottom carbon content specifications, which are by far the most difficult product specifications to meet for a diesel fuel product when employing nitrogenous treating agents. Furthermore, extraction reduces yields of product.
.
~3~00~
U.S. Patent No. 2,333,817 discloses oxidation of diesel oils by nitrogenous compounds followed by hexane dilution and filtering to improve cetane and prevent sediment formation. Such a product does not pass present~day indu~try standards for stability ~although haze formation is reduced) and it does not meet Ramsbottom carbon ~pecifications. From the exemplification it appears this techni~ue is only applicable to cycle oils.
These methods have generally apparently employed nitration or an oxidation treatment for cetane improvement of diesel oils, but lt is also ~nown that the cetane number of diesel oils can be increased by adding various nitrated hydrocarbon derivatives to the oils, including amyl nitrate, octyl nitrate, and the nitrate ester "dopes" disclosed in British Patent No.
491,648. Other nitrogen-containing additives for improving cetane are disclosed in U.S. Patent No.
4,398,505. Use of these derivatives is generally disadvantageous since they are expensi~e and must be separately prepared, handled and ~tored.
U.S. Patent No. 2,184,440 relates to methods of increasing the cetane number of blended diesel fuels by blending diesel fuels from different sources, one of which is a high sulfur crude, and treating the blended 130006~L
fuel with sodium plumbite and a large excess of elemental sulfur. Alternatively, a distillate fuel stock can be treated with ~odium plumbite and an excess amount o elemental sulfur over that reguired to sweeten the 6tock, and distilled to obtain a sweetened condensate, with the bottoms being further reduced and added to an untreated diesel fuel to increase the cetane number of the blend. The reduced bottoms amounting to about 1 to 6% of the original distillate fuel stock are added in amounts of about 0.5 to 5% to diesel fuels to raise their cetane number, e.g., by 2 to 19 over untreated diesel fuel.
U.S. Patent No. 2,104,919 provides a means to achieve a stabilized fuel by blending straight-run and cracked stocks. The disclosure of this patent states that typically fuel oils produced by blending straight-run components and cracked residues have a tendency to form a carbonaceous sludge on storage, and the precipitation of sludge in such fuels containing 10 to 80% heavy cracked residues is inhibited by mildly oxidizing the straight-run component before blending, e.g., by blowing air at 250-400C therethrough for l/2 to 12 hours.
U.S. Patent No. 2,317,96~ disclose~ a die~el fuel containing substantial portions of chemically combined ~30~t~6~
reactive oxygen through treatment with air, oxygen or an oxyyen carrying gas, to produce by partial oxidation a petroleum fuel having a volatility greater than that of kerosene and relatively free from asphaltic and resinous components and from large proportions of aromatics, to an "oxygen factor" of 800 to 1450 by air blowing, removal of acids produced by oxidation, and blending with a diesel fuel to produce a diesel fuel blend having increased cetane. Blends of 2.5% oxidized oil to 97.5% by volume sulfur dioxide-treated petroleum distillate and of 20% by volume of oxidized oil to 80%
by volume of a clean gas oil distillate are disclosed.
U.S. Patent No. 2,365,220 discloses a method similar to that o U.S. Patent 2,317,968. The disclosure is of the preparation of a diesel fuel, in which a diesel fuel of predominately paraffinic character is oxidized using air, oxygen or an oxygen carrying gas to produce an oil having an "oxygen factor" of higher than 5, acidic reaction products are rsmcved, and the resulting oxidized stock is blended with from 2/5 to 20 time~ its volume of a clean diesel petroleum hydrocarbon distillate.
U.S. Patent No. 2,521,698 discloses that the fuels produced by the methods of U.S. Patent Nos. 2,317,968 and 2,365,220 are unstable and corrosive, and that the ~31DOl)~
stability and corrosiveness of such cetane-enhanced diesel fuels can be improved with a loss of about 25%
of cetane enhancement, by subjecting the oxidized diesel fuel to acid treatment with a strong acid, such as sulfuric or nitric acid, in a concentration of at least 0.1 pound per gallon of ox$dized stock, followed by alkali wash and blending of the treated oxidized stock with diesel fuel. A concentrated oxygenated cetane-improving additive is also disclosed, prepared from the bottoms of the distilled oxidized diesel stock.
U.S. Patent 4,280,818 discloses oxidizing a hydrocarbon oil with aqueous nitric acid in a weight ratio of about 1:0.1 to 1:10 of hydrocarbon to acid and separating the aqueous phase from the oxidized hydrocarbon phase. The disclosure is that the oxidized hydrocarbon phase can be extracted and the product obtained blended with a polar solvent to produce a fuel mixture.
U.S. Patent No. 3,284,342 discloses oxidation of residue using a number of oxidants including nitrogen oxides, followed by a thermal treatment to reduce the sulfur content of the residue, in which both s-teps can be promoted with catalysts. When applied to diesel oil, this process produces substantial carbonaceous 01~6~
deposits in the thermal treating still, and is unsatisfactory for commercial use.
U.S. Patent 3,135,680 discloses a process for refining petroleum fractions in the diesel oil boiling range to produce diesel fuel with enhanced cetane number and odor by treating the fractions with nitrogen dioxide followed by a clay treatment to remove odor.
A process of deodorizing and desulfurizing light petroleum distillatss by treatment with nitrogen dioxide ollowed by alkali wash and water wash is disclosed in U.S. Patent No. 3,267,027. This process i~ unsuitable for producing diesel fuels of acceptable stability and Ramsbottom carbon content.
U.S. Patent No. 3,244,618 discloses a process for sweetening petroleum hydrocarbons by treating the hydrocarbon fraction with molecular oxygen in the presence of a catalytic amount of a nitrogen oxide.
Application of this process to diesel fuel results in a product with inferior cetane enhancement.
U.S. Patent No. 2,004,849 discloses the use of an oxidant, hydrogen peroxide, in combination with sulfuric acid to effect sulfur removal from hydrocarbons, without substantial loss of aromatics.
However, this process is ineffective for improving the cetane of di~sel fuel.
1~0(1 ~4 Processes for treating petroleum 6tocks by oxidation ~ollowed by solvent extraction have been described for various purposes.
For example, a process for producing a fuel composition by oxidizing a hydrocarbon oil with aqueous nitric acid, followed by extraction with acetone, methyl ethyl ketone, cyclohexanone, methanol, ethanol, normal propanol, isopropanol, ethyl acetate, tetrahydrofuran, dioxane, or a combination of an alcohol and a ketone, an alcohol and water, a ketone and water or a combination o alcohols is disclosed in U.S. Patent No. 4,280,~18.
Although the oxidation/extraction methods described above have met with some success in improving petroleum diesel fueLs, the known approaches toward oxidation to remove a portion of the original sulfur content as gaseous sulfur oxide~, and to convert a portion of the original sulfur content into sulfoxides and/or sulfones followed by extraction with appropriate solvents to achieve a desired low sulfur raffinate have not completely eliminated problems of in~tability and unacceptable Ramsbottom carbon for diesel fuels, and have the disadvantage of an expensive solvent extraction step, resulting in low yields.
13006)6A
The methods described above when applied to petroleum stocks for use as diesel fuels basically have the disadvantages that (a) oxidative desulfurization methods involving nitrogenous oxidizing agents often result in increased gum and sedimentation, and reduce the stability of the fuels produced, (b) the oxida-tively treated fuel~ are not useful as diesel fuel blendstocks due to poor stability and high Ramsbottom carbon content, and (c) solvent extraction, while effective to im~roVe stability and Ramsbottom carbon content, is expen~ive and of low product yield~ in comparison to oxidative treatment alone where the oxidized product alone can be blended to improve diesel fuels.
While many conventional methods of improving diesel cetane number by oxidation with nitrogenous oxidizing agents exist, they are generally inadequate to meet other product specifications. Particularly, diesel fuels produced by nitrogeneous oxidation and solvent extraction can in svme cases meet sulfur and cetane requirements for fuels, but are unsatisfactory with respect to the important specifications of stability and Ramsbottom carbon content. Processes employing sulfuric acid or clay in conjunction with nitrogeneous oxidizing agents are inefective to retain ~O~O~i4 a high cetane rating when pxacticed to control Ramsbottom carbon and stability. Distillative methods are commercially unfeasible due to the presence of substantial carbonaceous deposits in the still, and when thermal trea-ting is applied to diesel fuel to reduce sulfur content of the residue, this process also produces substarltial carbonaceous deposits in the thermal treating still. Often acceptable color levels in the product, particularly after storage, are not achievable.
Apart from the failure o conventional oxida-tive cetane enhancement methods to provide diesel fuels of sufficient stability and Ramsbottom carbon content, these methods, like the oxidative desulfurization methods, employ solvents which result in poor yields?
re~uiring unacceptably high solvent-to-oil ratios.
Alternatively, the sol~ent~ used in some methods reduce or entirely eliminate the advantage of cetane enhancement obtained by oxidation.
While certain of the patents cited above refer to oxidation of diesel stocks to improve cetane~ and the use o ~uch oxidatively enhanced stocks in blends with unoxidized diesel fuels, these patents fail to recognize the importance of limiting the nitrogen content of the final blend to achieve acceptable ~L3~00Ç;g~
stability or Ramsbottom carbon content in the final blend. Furthermore, there is no appreciation of the remarkable increase of cekane in the treated por-tion and in the final blend when nitrogen treatment and blending are controlled according to the present process. Finally, thare is no recognition o~ the further benefits of selected alkaline wash agents in imparting improved color stability while retaining the foregoing attributes.
SUMMARY OF T~E INVENTION
An object of the invention i8 to provide a process for enhancing the cetane number o a diesel fuel.
Another object of the invention is to provide a process for increasing the cetane number and improving the color of a diesel fuel e.g., preventing the development of color in the blend product over development of color in the blend product not subjected to the proces~ of this invention comprising treating the diesel oil with a nitrogenous treating agent, separating unreacted nitrogenous treating agent, treating the diesel oil with an inorganic alkali, and then blending the treated diesel oil with an untreated diesel oil in specific proportions to produce a blended diesel fuel having an unexpectedly increased cetane number and with marked improvement in the color of the ~30006~L
blended diesel fuel, compared to blending the treated oil without use of an alkali treating agent.
A further object of this lnvention is to provide a blended diesel fuel with improved cetane number and appropriate stability and Ramsbottom carbon.
An even further object of this invention is to provide a blended diesel fuel in which the amount of additive which might be added to enhance even ~urther the stability o~ the blended diesel fuel is minimized.
Also, an object of thi~ invention is to provide a process for producing a blended diesel fuel having good storage stability and color along with useful levels of Ramsbottom carbon.
When the alkali used for treatment is ln an aqueous solution form, a further object of the invention is to minimize the chemical oxygen demand in treatment of the spent alkali wash water for release in the environment or for recycle/reuse.
In one embodiment of this invention, this invention provide3 a process for the enhancement of the cetane number of and improvement in color developed on storage of a diesel fuel comprising:
(1) treating a diesel oil with a nitrogenou~
treating agent in a nitrogen amount, equivalent on a 100% nitric acid basis, to ~..3~
about 10 weight percent or less of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (1~;
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated diesel oil of step (3) wlth an untreated diesel oil to produce a blended diesel uel ~uch that the nitrogen added content in the blended diesel fuel is (a) about 300 ppm or less of nitrogen added when the diesel oil treated in step (1) is obtained from virgin diesel oil stock, or (b) about 450 ppm or less of nitrogen added when the diesel oil treated in step (1) is obtained from hydrotreated diesel oil stock.
In a further embodiment of this invention~ this invention provides a process for the enhancement of the cetane number of and improvement in color developed on storage of a non-fungible diesel fuel comprising:
(1) treating a first diesel oil with a nitrogenous treating agent in a nitrogen ~3()0~4 - ~6 -amount, equivalent on a 100% nitric acid basis, to about 10 weight percent or les~ of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent rom the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated dieseL
oil; and (4) blending the treated diesel oil of step (3) with a second diesel oil which has not been treated as in step (1) above to produce a blended diesel fuel such that the nitrogen added content in the blended diesel fuel is about 1,000 ppm or less of nitrogen added, and : ~ wherein the first diesel oil treated in step (1) and/or the second diesel oil blended in step (4) and/or the blended product o step (4) is a non-fungible diesel fuel.
BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWINGS
Figure 1 is a graph showing the relationship between ASTM color and age of the diesel fuel blend : ' produced by the process of this invention.
Eigure 2 is a graph showing the relationship between Nalco stability and amount of stability 0~4 improviny additive present in a diesel fuel blend produced by the process of this invention.
Figure 3 is a graph showing the relationship be-tween Ramsbottom carbon and nitrogen added to the diesel oil blend.
Figure 4 is a graph showing the relationship between stability and nitrogen added to the blended diesel fuel.
Figure 5 i8 a graph showing the average blending cetane numbers of blended diesel fuel products for varying amounts of treated diesel fuel in the blend.
Figure 6 is a graph showing the calculated pool cetane of blended diesel products produced.
DETAILED DESCRIPTION OE THE INVENTION
As indicated above, the process of this invention involves, in particular, enhancement of the cetane number of a diesel fuel and improvement in color developed on storage. The process basically comprises:
(1) treating a diesel oil with a nitrogenous treating agent in a nitrogen amount, e~uivalent on a 100~ nitric acid ba~is, to about 10 weight percent or less to the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (l);
(3) treating the diessl oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated oil of step (3) with a diasel oil which has not been so treated as in step (1) to produce a blended diesel fuel such that the nitrogen added content in the blended diesel fuel (a) is about 300 ppm or less of nitrogen added when the diesel oil treated in step (1) is a diesel oil obtained from virgin diesel oil s~ock, or (b) is about 450 ppm or less of nitrogen added when the diesel oil treated in step (1) is a diesel oil obtained from hydrotreated diesel oil stock.
In the first step of the process of this invention, a diesel oil is treated by contacting such with a nitrogenous treating agent in a nitrogen amount equivalent to about 10 weight percent or less on the diesel oil feed of nitric acid based on the nitrogen content of a 100% concentration nitric acid.
If desired, the feed oil can first be subjected to pretreatment, 8uch as by washing to remove phenols or other corrosive components of the oil, filtering to ~00~4 remove gum or sediment, or heating or treatment with H2S04 as conventionally used. In the fir~t step of the process of the invention, the treating agent is a nitrogenous treating agent. The term "nitrogenous treating agent" is used herein to mean any known nitrogen-containing oxidizing compound including, e.g., a gas containing at least one nitrogen oxide with more than one oxygen atom for each nitrogen atom, a liquid containing at least one nitrogen oxide with more than one oxygen atom for each nitrogen atom, nitric acid and nitrous acid.
The treating gas used can be a gas containing only such a nitrogen oxide or can be one which contains mixtures of such nitrogen oxides. Furthermore, the treating gas can be one which also contains other components such as oxygen, nitrogen, lower nitrogen oxides, i.e., nitrogen oxides containing only one oxygen atom or less than one oxygen atom per nitrogen atom in the oxide. For efficiency, preferably the treating gas will be one which contains only nitrogen oxides with more than one oxygen atom for each nitrogen atom but mixtures with other gases such as oxygen, nitrogen, as well as inert gases such as air, helium and helium with air can be employed if desired.
Suitably the treating gas will contain at least 0.5% by ~3~ i4 volume of at least one nitrogen oxide with more than one oxygen atom for each nitrogen atom, but the concentration can be reduced if the flow rate of treating agent is increased for a longer time.
Nitrogen dioxide or its dimer N204 can be advantageously employed, alone or in a admixture with air.
The nitrogenous treating liquid used can be li~uid ni-trogen oxides as defined above, nitric or nitrous acid either concentrated or in admixture with up to about 90% water by weight. Preferably the liquid nitrogenous treating agent is an a~ueous solution of nitric acid containing about 50 to 90% by weight nitric acid.
However, the above described concentrations, e.g., nitrogenous treating agent concentrations, are not limiting and are given merely for exemplification.
Basically any concentration can be used as long as the nitrogenous treating agent is present in sufficient amounts to achieve in the blended product the nitrogen added amounts for the process of the invention when the treated diesel oll is blended with the untreated diesel oil.
When liquid nitric acid is used as a nitrogenous treating agent in the present invention, it may ~3~0~
advantageou~ly be used in combination with other organic or inorganic acids. Suitable inorganic acids include sulfuric and phos~horic acids, and suitable organic acids include, e.g., acetic and formic acids.
The organic and inorganic acid may be used alone or in combination. Typically, an inorganic acid can be added to the aqueous nitric acid solution used as a trea-ting agent in an amount of fxom about 5 to 200% by weight of the nitric acid solution, and an organic acid can be added in an amount from about 5 to 200% by weight of the nitric acid æolution. Preferred combinations of nitric and au~iliary acids include nitric and sulfuric, nitric and acetic, and nitric and formic acids.
When liquid nitrous acid is used as a nitrogenous treating agent in the present invention, it may advantageously be uæed in combination with other organic or inorganic acids. Suitable inorganic acids include sulfuric and phosphoric acids, and suitable organic acids include, e.g., acetic and formic acids.
The organic and inorganic acid may be used alone or in combination. Typically, an inorganic acid can be added to the aqueous nitrouæ acid æolution used as a treating agent in an amount of from about 5 to 200% by weight of the nitrous acid ~olution, and an organic acid can be added in an amount from about 5 to 200% by weight of 1~ 0~4 the nitrou~ acid solution. Preferred combinations of nitrous and auxiliary acids include nitrous and sulfuric, nitrous and acetic, and nitrous and formic acids. Mixtures of nitric acid and nitrous acid can also be used.
In the first step o the process of this invention, a diesel oil such as atmoæpheric gas oil is reacted with a nitrogenous treating agent in the form of a liquid or gas. The contacting of the diesel oil with the treating liquid can be accompli~hed by any means conventional in the art or contacting two liquid reactants, e.g., by injecting the acid mixture under the surface of agitated oil contained in a reactor.
When a treating gas is employed, the treating gas can be contacted with the diesel oil using any conventional means for contacting a gaseous reactant with a liquid reactant. Suitable examples of such means for contacting a gaseous reactant with a liquid reactant include dispersing the gas as bubbles in the li~uid, trickling the liquid over an inert solid bed with gas passing also over the bed co-currently or countercurrently to the liquid flow, the latter type flow being preferred.
It is important in the first step of the process of thi~ invention to control the operating parameters 130~ Ei4 during the reaction of the diesel oil with the treating gas or liquid to insure that the nitrogenous treating agent is employed in a nitrogen amount e~uivalent to about 10 weight percent or less, preferably 6 weight percent or less, more preferably 5 weight percent or less, of nitric acid based on the nitrogen content of 100% nitric acid. In accordance with the process of the present invention, by conducting step (1) in this manner and in combination with steps ~2) and (3) described hereinafter, this results in a product of extremely high cetane value which may be advantageously blended into a dlesel pool without deleterious effects on Ramsbottom carbon and ~tability. This important processing control as to the reaction of the diesel oil with the nitrogenous treating agent is described in more detail below.
As used herein, the term "nitric acid e~uivalent-to-oil ratio" (acid-to-oiL ratio, A/0) refers both to the weight of water-free nitric acid to the weight of diesel oil feedstock and to the weight of undiluted gaseous or liquid nitrogenous treating agent to the weight of diesel oil feedstock, and is from about 0.0002 to 0.10, preferably from about 0.0005 to 0.05, for the acids and from 0.0002 to 0.10, preferably 0.0005 to 0.05, for the nitrogen oxides. The control 5~
of the trea-tment may be achieved by controlling the water content of the acid in the reactor, by controlling the mixture of nitrogenous gas and air or inert gas used or by controlling temperature, time and degree of agitation. The treatment can also be controlled and improved by the copresence of sul~uric acid through itF9 effect on water availability or other auxiliary acid mixed with the treating agent. This control of the amount of nitrogenous treating agent to the total weight of the diesel oil feed in step (1) can be easily maintainéd.
The reaction of the first step of the present invention can be performed at any temperature from about -40 to about 200C, or less, moet preferably from about 25 to 90~C. The reaction time is not particularly limited, and may include9 for example, any time from about 1 minute to about 3 weeks. This first step o the present invention may be conducted at atmospheric pressure or at greater or lower pressures as de~ired. Advantageously, the reaction step is conducted using conventional agitation means, such as a stirrer or such as a pumparound reactor.
Since a nitrogenous treating agent is used in the first step of the present invention, typically an increase in nitrogen compound content over that ~3~
originally present in the diesel oil will be observed.
While not desiring to be bound by theory, the reason for the increase in observed nitrogen compound content is believed to be that nitration and esterification of the diesel oil substrate can occur resulting in an increase in the heteroatom nitrogen compound content.
~ ecause of the complexity o the reactions involved, the treating agent~ may well do more than oxidize or nitrate compounds contained in the diesel oil in the process according to the invention. Hence, the first step is variously described herein as "nitrogenation" or simply "nitrogen treatment" or more simply "treatment", which refers to any reaction of the nitro~enous treating agent and diesel oil or its components, without limitation, and without reliance on any particular reaction or reaction mechanism.
Contact times on the order of less than about 120 minutes and weight ratios of nitrogenous treating agent to diesel oil feed o less than about 0.1 are desirable not only from the standpoint of efficiency hut also from the standpoint of economics. Particularly preferably, a contact time of ahout 30 minutes in combination with a weight ratio of nitrogenouæ trea-ting agent to diesel oil feed of about 0.05 or less can be o~
advantageously employed for maximum yield of diesel oil with improved ce-tane rating and useful stability.
However, because of the known :relationship of nitrogenous treating agent to cetane number, it i9 often advantageous when using a nltrogenous treating agent to carefully control the minimum amount of nitrogen compounds added to the diesel feed in order to insure a suficient cetane number in the diesel fuel produced.
Depending on the nature of the nitrogenous treating agent employed, one ~killed in the art can easily determine the amount o nitrogenous treating agent to use to ensure the proportion employed i 6 a nitrogen amount equivalent to 10 weight percent or less nitric acid based on the weight of the diesel oil fed as a eed stock in step (1) of the process of this invention.
The process of this invention is applicable to the upgrading of diesel oil which can be derived from any source, for example, a conventional petroleum crude oil or crude oil fraction containing sulfur, aromatic, olefinic and naphthenic compounds as impuritles. The term "die~el oil" as used herein is broadly deEined to include any hydrocarbon having a nominal boiling range of about 350F to 700F which can be upgraded by the 1~0~4 process o this invention to meet commercial speciications for a diesel fuel and the term "diesel fuel" is ~enerally used to describe the upgraded product, although the terms can be used interchangeably.
The process of this invention is basically not limited in term~ of the source of the diesel oil, but is applicable to any diesel oil from petroleum, coal, shale, tar sands, etc.
In the process for upgrading diesel oils accord:ing to the invention, particular product specifications may vary over a range. Based upon the disclosure contained herein, the present process may be readily applied and modified by one skilled in the art to produce a blended diesel fuel having particular desired specifica-tions, particularly with respect to the basic criteria of cetane, stability, Ramsbottom carbon and sulfur content, density and boiling range. Furthermore, the process of this invention can be employed in combination with conventional techniques for meeting product specifications as desired, e.g., by addition of chemical additives such as corrosion inhibitors, stabilizer~ and the like.
Fuel stability is measured by a number of accelerated tests, one of which is the Nalco 300F
~o~!Ei4 test. For satisfactory stabili.ty in commercial storage and use, a transportation fuel must exhibit a Nalco rating of about 7.0 or lower. A rating of about 7.0 is the upper level of acceptability for commercial use, although a lower limit is desirable. The applicable Nalco test is well known in the art, and the test can be simply performed, for example, by placing 50 ml of oil to be tested in a tube 3 cm in diameter, heating the tube in a 300F bath for 90 minutes, and then cooling the oil. The oil i~ then filtered using a micropore filter with a number 1 filter paper, the filter and the filter paper are washed with heptane, and the residue remaining is compared with standard samples to determlne the stability rating. If a fuel has a Malco rating exceeding 7, it may often be blended with other ~tocks or treatsd with economic levels of chemical additives to bring it into specificat1on.
This approach can be smployed with the blended fuel product produced by the process of this invention as well.
In addition to management of the above criteria of stability and cetane number, Ramsbottom carbon content is an important ~uality speciication for diesel fuels, since fuels high in Ramsbottom carbon cause fouling problems when used in diesel engine~. In an acceptable ~30~ 4 diesel fuel, the Ramsbottom carbon content is preferably less than about 0.3 weight per cent, as determined by the method disclosed in ASTM D 524, prior to addition of any nitrate additives for cetane improvement.
Nonfungible fuels also have commercial importance, such as dedicated uses for railroad engines and the like. In these applications, fuel specifications, for example, Ramsbottom carbon and stability can be grea-tly relaxed from those discussed above, such as permitting a Ramsbottom carbon content o, for example, about 1 to about 10%. For these cases, the present inven-tion still finds important applicabillty at appropriately elevated levels o nitrogen added.
While not desiring to be bound by theory, it is currently believed that the complex process according to the pre~ent invention for upgrading diesel oils by contact with a nitrogenous treating agent probably involves nitrogen addition to paraffins, olefins, naphthenes and aromatics to form nitrates, esters, amines, azides, indoles and the like.
As indlcated above, the process of this invention can be employed on an atmospheric gas oll fraction derived from li~uid petroleum crude sources.
Atmospheric gas oil is one component used in diesel oil ~1~31)~
blending, and may contain an off-specification sulfur content for use as a diesel fuel. Typically, ~ulfur as a heteroatom i9 present as thiol.s, di~ulfides, sulfides, thiophenes, and mercaptans, and nitrogen is present a~ substituted pyridines and pyrroles, and other compounds. A typical analy~is of atmospheric gas oils is set forth in Table 1 below.
13~
Table 1 Properties of Atmospheric Gas 0i1 (AGO) and of Liqht CYcle Oil (LC~
Stock H Stock I LCO
Gravity, API 33.1 34.2 17.65 Sulfur, wt.% 0.5 0.460.77 Nitrogen, ppm 156 191 679 Ramsbottom carbon, % 0.156 0.105 0.620 Nalco* 1 2 2 Cetane Number 46.0 41.0 22.7 D86 Distillation, F
start 290 250 430 5% 410 380 465 10% 435 395 490 30% 487 450 530 50% 517 490 550 70% 550 540 570 90% 602 600 625 95% 676 640 650 After the completion of the treatment of the diesel oil With the nitrogenous treating agent in step (1) of the process of this invention, unreacted nitrogenous treating agent is separated from the diesel * trade mark fuel in step (2). Where excess nitrogenous treating agerlt is separated, this can be achieved by decanting of the residue phase, by strippin~ of the nitrogeneous treating agent, or by other techniques well known to one skilled in the art or combinations of these physical removal techniques.
In step (3) of the process of this invention, the diesel oil from step (2) is treated with an inorganic alkali preferably an alkali metal hydroxide or a~monium hydroxide or mixtures thereof. Preferably a solution, e.g., an aqueous solution, of the inorganic alkali is employed. Where a solution is employed, a suitable concentration of alkali in the alkali solution is about 0.01 to about 5 M, more preferably 0.05 to 2.0 M, even more preferably 0.5 to 2.0 M, and most preferably 0.5 to 1.0 M. The alkali solution is used in a weight ratio to the diesel oil of step (2) of about 0.01 to l:l, preferably 0.08 to 0.5:1, most preferably 0.08 to 0.15:1.
A preferred inorganic alkali is ammonium hydroxide since it has been found, as is shown in the examples yiven hereinafter, that the chemical oxygen demand (COD) of the wash separated from the diesel oil in step (2) in treatment for environmental release or reuse is markedly reduced.
- 33 - ~
The treating of the treated diese]. oil from step (2) with the inorganic alkali can be achieved by simply mixing the diesel fuel obtained in step (2) with the alkali. Any conventional means for achieving effective contact, such as co-current or countercurrent flow or a simple addition with agita~ion, can be employed to treat in step (3) the diesel oil from step (2). Although not essential, if desired, the diesel oil of step (3) can be subjected to a water washing step prior to use of the treated diesel oil of step (3) to produce the diesel fuel blends of ~tep (4).
In the next step (4) of the process of this invention, the treated diesel fuel so obtained is then mixed with a diesel oil which has not been BO treated, herein "untreated diesel oil", to produce a blended diesel fuel.
Examples of untreated diesel oils which can be used and mixed with the treated diesel fuel obtained in step (3) include any diesel oil with a boiling range of about 350F to about 700F. While in the process of this invention, any untreated diesel oil as previously described can be blended with the treated diesel fuel obtained in Step (3) above to achieve cetane enhancement and improved color development on storage, it would be obviou~ to one skilled in the art that the ~3~ 4 properties of the untreated diesel oil to be blended must be taken into account such that when the blend product is produced, other specifications required for a commercial fuel, such as sulfur content, Ramsbot-tom carbon content, stability, and the like, are met.
In order to enhance the cetane number of the ultimate diesel fuel blend, the nitrogen content added into the blended diesel fuel comprising the mixture of the treated diesel uel and the untreated diesel oil is carefully controlled in accordance with the ollowing parameters.
SpeciEically, where the diesel oil feed to step (l) is obtained from virgin diesel oil stocks, such as atmospheric gas oil, the amount of nitrogen added into the blended diesel fuel is about 300 ppm nitrogen or less, generally 150 ppm or less, more generally 100 ppm or less..
Where the diesel oil feed to step (1) is obtained from a diesel oil from hydrotreated diesel oil stocks, such as an atmospheric gas oil treated with hydrogen in the presence of a cataly~k at a temperature exceeding about 600F and a pressure exceeding about ~00 psi, the amount of nitrogen added into the diesel fuel blend is about 450 ppm nitrogen or less, generally 300 ppm nitrogen or less, more generally 200 ppm or less. The 1~ 4 minimum amount of treated diesel oil prepared in steps (1), (2) and (3) which i~ employed in the blended product produced in step (4) is at lea~t about 5 ppm nitrogen added, whether the diesel oil ~tock treated in step (1) is from virgin diesel oil stocks or hydrotreated diesel oil stocks.
Where the blended diesel product is to be used as a nonungible fuel, i.e., where the fuel i5 produced for a specific end use and thus adherence to normal specifications of a fungible commercial diesel fuel are not of concern, then the diesel oil feed to step (1) can be any refinery stock having appropriate properties such that when subjected to the process of this invention provides blends meeting nonfungible specifications in the final product blend. In this case, the nitrogen added due to the treated diesel oil of step (3) in the blended product can be such that the diesel fuel blend contains about 1000 ppm or less of added nitrogen, generally 800 ppm or less of added nitrogen, more generally 600 ppm or less of added nitrogen Use of the treated diesel oil in the blend produced with more than the above described levels of nitrogen added to the blend results in the inability to meet the desired blended product specifications for a diesel fuel.
The diesel oil stocks used to which the present invention is applicable can vary widely, and specifically can contain initial nitrogen levels from as little as about 5 ppm up to levels of about 1000 ppm. Surprisingly, even though it is conventionally believed there is a relationship of cetane to nitrogen level of a fuel, it has now been found that as a result of this invention it is no-t the total nitrogen content of the product blend which is relevant to simultaneous control of cetane, Ramsbottom carbon, and stability of the fuel product. Without regard to the nitrogen content of the ultimate blend obtained, the amount of added nitrogen i8 the relevant parameter to be controlled. Added nitrogen is defined herein as the nitrogen content of the final blended product after step (4) less the nitrogen content of the untreated diesel oil stock used in step (4) before addition of treated diesel oil obtained from step (3).
Regarding the blendability of Ramsbo-ttom carbon content, it must be recognized that ASTM procedures reguire that the fueL first be distilled, and the carbon measurement then be made on the 10% bottoms remaining (by pyrolysis). This is because the Q~
Ramsbottom carbon precursors are normally found in the bottom cut of the die~el fuel. By concentrating these precusors by distillation, the precision of the carbon measurement is greatly improved. If another low Ramsbottom stock is blended, Ram6bottom carbon is not necessarily reduced because that blend-stock is distilled out before carbon measurement. Blending a heavier stock with the high carbon content stock ~so that the bottom 10% i~ relatively dilute in carbon-forming compounds) might be contemplated but this would violate the ASTM end point specifications on the diesel fuel. Fur~hermore, for nitrogenated stocks produced in the process of thè present invention, the nitrogen compounds are known to be polymerization catalysts for carbon formation, so that small amounts produce signiicant Ramsbottom carbon even when diluted.
As to stability of diesel fuels, the stability of diesel fuels and blends of diesel fuels are generally improved by the addition of certain stability addi-tives. Use ul additives include alkyl amines in either a petroleum or polymeric solvent. The amine functional groups in these additives are predominantly found in high molecular weight molecules containing either branched chain alkyl or allyl groups. Dupont, UOP, and 13~
Ethyl Corporation produce additive~ of this general composition, although the specific compositions of such additives are generally proprietary. sorg-warner Chemicals market~ an additive which has a phenolic base structure, while Petrolite Corporation produces an alkylamine-iodine base additive ~n an acrylate polymer and xylene solvent as stability additives to diesel fuels. Table 2 summarizes known compositional details of these commercially available additives.
It has also been found that when conventional stability additives are employed with the blended diesel fuel product produced by the process of the present invention, the levels required to achieve acceptable stability results are unexpectedly reduced.
More specifically, the Petrolite commercially available stability additive (Petrolite T-363), provided the best stability improvement response for a given stability additive level. Reduction of the ASTM
D 2274 oxidation stability rating by 47%, 67% and 81%, using stability additive levels of 60, 100 and 150 ppm (based on the blended diesel fuel product obtained in this invention) at 3% by weight of the diesel oil product of step (3) in the blend diesel fuels of step (4), re~pectively were aGhieved, with only 60 to 80 ppm being re~uired to provide an adequate stability.
1~0~
Similar stability improvements at 6tability additive levels in the 60 to 80 ppm range were also achieved wi-th other Petrolite additives and would be expected over the entire range to 150 ppm.
Although the other amine based commercially available additives, e.g., those produced by Dupont, UoP, and Ethyl improved stability, this improvement was less than that achieved with the preferred commercially available Petrolite products for the same additive level. However, acceptable stability could be achieved at a higher ppm level than for Petrolite.
A reduction in the stability additive requirement to about 25% to 75%, more typically 33% to 50%, for the blended product produced in the present invention, where the product of step (3) used to produce such blend of step (4) is subjected to the inorganic alkali treatment as in step (3) in comparison with a blended product produced where the product used in producing the blend of step (4) is not so subjected to an alkali treatment as in step (3). The inorganic alkali treatment of step (3), therefore, reduces the stability additive level re~uirement from, for example, about 60 to 80 ppm down to about 20 to 40 ppm level, to give a suitable stability based upon a product blend with a blending of 3% by weight of the diesel oil of step (3) 13(J 0~
in producing the diesel uel bl~nd of step (4) of thiæ
invention.
As a result, it can be seen that the process of this invention provides the ability to reduce the amount of stability additive to levels of about 25% to 75%, more typically 33% to about 50%, of the amount of stability additive which would be employed in the absence of the inorganic alkali treatment of step (3) of the process of this invention.
~3~ 64 Table 2 Compo~itional Summary o CommerciallY Available StabilitY Additives Additive TyPe Chemical Compo~ition Petrolite T-260 Organic amines Petrolite T-316 Organic amines Petrolite T-362 Organic amines Petrolite T-363 Alkyl amine-iodine base with acrylate polymer in xylene Petrolite T-386 Organic amines UOP Polyflo T121 N-~l-methylheptyl) ethanol amine N,N' di~alicylidene-1,2-propane-dlamine in a naphtha solvent UOP Polyflo T122 Polyamino polyol N-(l-methylheptyl) ethanol a~m:Lne N,N' disalicylidene-1,2-propane dlamine in a naphtha ~olvent UOP AID T2525 High molecular weight amine polymer and petroleum solvent UOP Polyflow T120 Similar to Polyflo T121, but without a copper deactivator.
Dupont E'uel Oil Additive $~3 Organic amine Borg Warner Ultranox 226 2,6-di-t-bukyl-4~methylphenol Borg Warner Ultranox 236 4,4'-thio-bi~(2-t-butyl-5-methylphenol) Borg Warner Ultranox 246 2,2'-methylene-bis(4-methyl-6-t-butyl phenol) Borg Warner.Ultranox 254 polymeric 2,2,4-trimethyl-1,2-dihydroguinoline Borg Warner Ultranox 256 polymeric ~3terically hindered phenol Figure 1 shows the effect of storage on the blended diesel fuel resulting from step (4) of the process of the present invention as a function of ASTM
color (D-1500) in relation to time where the treated diesel oil of step (1) is washed with water or is treated with an agueous sodium hydroxide solution. It is surpising that by using the aqueous alkali solution treatment after the treatment with nitrogenous treating agent in step (1) and separation of excess nitrogenous treating agent in step ~2) but prior to blending in step (4) results in the marked improvement in color of the blended diesel fuel on storage. This is particularly true since treatment with inorganic alkali in the form of an a~ueous solution does not appear to initially have much effect on the color of the dlesel oil obtained in step (3).
Considering the background of stability and color formation of diesel oils, the mechanisms are not well known except in general terms. It is, however, recognized that trace levels of contaminants, such as nitrogen compounds, play an important role in sediment formation, often as catalysts. They may also play a role in color development. As a result, as to stability, dilution of an unstable fuel by a stable fuel does not generally improve stability appreciably.
~3~)0~
Upon dilution by a stable uel, there are still suffi~ient quantitie~ of these initi~tors to cause stability problems. Increased color on storage may also result. As a re6uLt, the conventional method to attack stability pxoblems has been to use a range of antioxidants, with the choice of the appropriate antioxidants being selected empirically (governed by which mechanism is operative or a given stock).
Unfortunately, for nitrogenated stocks, uneconomic levels o additives have been required in the past.
It has also been found in this invention that when such stability improvqng additives are used, the amount thereof necessary in the blended diesel fuel produced by the proceæs of this invention can be markedly reduced. Thi~ effect i8 6hown in Figure 2 discussed below.
Figure 2 demonstrates that the amount of stability additive to the diesel fuel blend obtained in step (4) of the process o this invention can be markedly reduced by using the treatment with inorganic alkali of step (3) of the process of this invention. For example, the amount of additive, Petrolite T-363 in (ppm) to achieve a particular Nalco stability for the alkali treatment using an aqueous solution of ammonium hydroxide is markedly reduced in comparison with the ~L300~
amount of additive required for the same Nalco s-tability where the treatment in step (3) of the process of this invention i~ simply a water wash.
Figures 3, 4, 5 and 6 clearly show graphically the above advantages of the process of thi~ invention in terms of cetane enhancement and stability of the blended fuel product obtained in accordance with the trea-tment with nitrogenous treating agent step, the removal of excess nitrogeneous treating agent step and the blending step as disclosed in parent application Serial No. 832,196, iled February 24, 1986, the disclosure of which is incorporated herein by reference. The addition o the alkali treatment step between separation of the nitrogeneous treating agent step and the blending step as in this invention does not substantially change the nature of the improvements in cetane number enhancement achieved but additionally provides the ability to unexpectedly minimize color development of the diesel fuel blend as shown in Figure 1 and reduce the amount of any affirmatively added stability enhancer which might be used as shown in Figure 2. As long as the nitrogen added levels adhered to set forth in step (4) above are as to the relationship of the amount of treated diesel oil o step (3), used in the blend of step (4~, the same 136~ 4 general cetane enhancements achieved in the process of said parent application Serial No. 832 J 196 are achieved with the process of this invention and surprisingly the amount of color developed on storage of the blend of step (4) i5 minimized as shown in Figure 1 hereof. The presence or absence of an alkali treatment step does not substantially affect the cetane enhancement, characteristics achievable, etc.
To illustrate the cetane enhancement, stability, etc., characteri#tics achievable in the process of this invention, reference more specifically is made to Figures 3 to 6 below~
To obtain the data shown in Figures 3 and 4, the diesel oil of step (2) was blended with an untreated oil to produce a blend product. Since the oil of step (2) contained nitrogen at levels of 2000 to 4000 ppm, the this oil was employed in the blend at about 2% to 15% by weight of the total blend. Analogous results to those shown in Figures 3 and 4 are achieved when an alkali treated oil of step ~3) is used to produce a blend product. The prior art has variously reported cetane number improvements of 5 to 20 numbers. Figure shows blending cetane number~ achieved generally corresponding to data with less than about 15% by weight treated oil in the blend. Since the di~sel oil 130~4 feed had a cetane number of about 40, the product oil of step (2) or of step (3) would be e~pected to have a cetane number o~ 45 to 60. Quite aurprisingly, cetane numbers of 60 to 220 are achieved when blend proportions of lesa than 15% by weight of the oil obtained in step (2) or in step (3) are used in producing the diesel fuel blend product. However, it is to be emphasized the blend proportion used in Eigure was employed only for purposes of illustration.
Various other combinations of treating reactor variables and blend proportions to provide appropriate levels of added nitrogen as herein defined can be employed.
As will be discussed below, the line through the data of Figure 5 may be used to describe the cetane number of oils produced in step ~2) and by analogy in step (3) of the present invention. For these runs, this corresponds to blend proportions of less than 15%
by weight. When the cetane of the final blend of diesel fuel obtained is calculated from the curve shown in Figure 5 to eliminate scatter, the resulta of Figure 6 are obtained. In view of the very ~mall amounts of step (2) and by analogy of step (3) oil used, it is very surprising that a large improvement in cetane of the blended diesel fuel product is achieved.
0~;4 In particular, a 3 cakane number increase in the diesel fuel hlend produced is obtained. Furthermore, it is particularly surprislng that the maximum in the cetane curve resides in the blend region where Ramsbottom carbon content and stability are simultaneously controlled.
Figures 1 through 6 indicate surprising and unobvious results, particularly by considering the weight of the combination o these effects. It is surprising that blends with added nitrogen having acceptable Ramsbottom carbon also provide blends of acceptable stability, with large cetane improvement and with a maximum cetane in regions of excellent stability and Ramsbottom carbon as well as improved blend color development on storage, i.e., less color developed, as discussed above.
The treated diesel oil from step (1) of the process of this invention can typically contain from 2000 to 4000 ppm nitrogen. The measured cetane ratings of such treated oils generally is 44 to 50 with an initial cetane rating of 40 for the diesel oil feed to step (1), with an improvement over step (1) diesel oil feed (40 cetane) of 4 to 10 cetane numbers, similar to that which would be expected rom the prior art. If the nitrogen added data are considered for an untreated ~3~)0~)~4 - 4~
feed o 100 ppm nitrogen to produce the diesel uel blend, simple calculations reveal that less than about 20% by weight and usually less than about 10% by weight of treated diesel oil can be accommodatled in the blend.
With such a low blend percentage o treated diesel oil, it would not be expected that the blended diesel fuel product could have a cetane improvement beyond about 1 number ba~ed on conventional knowledge. Nevertheless, a surprisingly large cetane improvement was obtained.
Further, if the cetane i8 measured of the blended diesel fuel product, the blending cetane value of the step (2) and by analogy of step (3) diesel oil can be back-calculated from the well-known linear blending equation. The surprisingly large cetane improvement of the diesel fuel blend produced leads to extremely large apparent blending cetane ratings for the diesel oil product obtained from step (2) or step ~3). Whereas conventionally, cetane improvements of the die~el oil product of steps (1), (2) and (3) of about 10 cetane numbers might be predicted and such valu~s were indeed measured for pure diesel oil product of step ll), the blending cetane values of the diesel oil product obtained after conducting steps (1), (2) and (3) are markedly increased.
~ 3(~0~Ç~4 With these dilute dies~l blends, little cetane improvement would have been expected. However, as shown in Figure 5, the effective cetane rating of the diesel oil product used in the blend produced becomes surprisingly large for the~e dilute blend~. Not only do these blends exhibit useful Ramsbottom carbon and stability under the nitrogen added criteria of the present invention, but a~so the cetane level of the diesel fuel blend i8 maximized as shown in Figure 6.
The blended diesel fuel obtained in accordance Wit}l the process of this invention can be used in any application wherein a diesel fuel meeting commercial specifications is desired. For example, the blended diesel fuel can be used as fuel for automotive, motor truck, railroad or marine diesel uses.
The following examples are given to illustrate the process of this invention in greater detail. ~owever, these examples are not to be construed as limiting the scope of the present invention but rather are given to merely illustrate the present invention. Unless otherwise indicated herein, all parts, percents, ratios and the like are by weight.
Example 1 To provide the data of Figures 3 through 6, diesel oils were fed to a treating reactor, consisting of individual stocks selected from those shown in Table 2 for each run~ These products were decanted to separate a re~idu~ phase a~ discussed below to produce a treated diesel oil. This oil was then blended with individual stocks A, B, or C selected from those described in Table 3 shown below to produce a blended diesel fuel.
The designations in Figure 3 show the nontreated diesel fuel used to blend with the treated diesel oil. Note that the treating reactor die~el oil feed, ~tocks A
through G of Table 3, contained widely varying amounts of nitrogen.
In each one o the runs, about 500 grams o diesel oil was placed in a 1000 ml volume reactor which consisted of a beaker with a septum on the side.
Nitric acid was used as the nitrogenous treating agent.
The septum was about 1 inch from the bottom surface of the reactor for nitric acid injection. A measured ~uantity of 90% nitric acid (5.5g for 0.01 A/0, 16.5g for 0.03 A/0, 2.75 for 0.05 A/0, and 33g for 0.06 A/0) was placed in a syringe and mounted on an in~ection pump. Here, A/0 designates the acid to oil weight ratio used. The oil was stirred with a lab size stirrer at 1000 RPM. The temperature o the mixture was controlled at specific levels between 25C and 80C
for these runs. Acid was injected over a 30 minute ~3003~
period. After the acid injection, the reaction mixture was further stirred for an additional 30 minutes to ensure consumption of residual acid in the mixture. A-t the completion of the treatment, the oil was separated from the residue formed by simple decantation. The separated oil was weighed~ water washed and filtered.
A specified amo~nt of oil was blended with one of the untreated diesel oils shown in Table 3. Depending on the A/0 ratio and treatment temperature used, different percent blends were made to be able to generate the relationships among variables shown in Eigures 3 to 5.
Samples of the blended products were analyzed for cetane number (ASTM D613), Ramsbottom carbon (ASTM
D524~, and Nalco stability. With 0.01 A/0 ratio usually the nitrogen content of the treated oil is about 1500 to 2000 ppm; with A/0 = 0.03 the nitrogen content of the treated oil is about 3000 to 4000 ppm and for A/0 = 0.05 the nitrogen content of treated oil is about 5000 to 6000 ppm. With A/0 = 0.01, 5 to 10 percent blends were made (N added = 75 - 150 ppm).
With A/0 = 0.03, 3 to 5 percent blends were made (N
added = 100 - 150 ppm) and with A/0 = 0.06, 1 to 2 percent blends were made (N added ~ 60 - 120 ppm) The results obtained are shown graphically in Figures 3 -to 5.
~OO~
Tablo 3 Propertles of VariouJ Dlesel Oil 5tot:ks Low Pressure ~loderate Pre3sure Ill~h Pre3~uro Strai~ht Run Dle~el _ydrotreated ~59~ Hydrotreated E F ~; C_ A B D
Gravity,API 34.637.6 32.4 38.8 36.3 34.2 30.8 Sul~ur, wt% 1.070.72 1.08 0.09 0.60 0.46 0.0 Nitrogen ~ ppm200 150 93 96 191 256 87 llam~bottom t~arbon % O.IZ90.144 0.139 0.122 0.111 0.105 0.107 N~lt70 - - 2 4 1 2 2 Cetane Number 58 53 48 39.2 41.7 41 38.8 D86 D1stlllat1On, F
Start216 300 270 405 Z50 380 5% 418 408 440 41~ 380 410 10% 4~12 446 468 440 395 426 30% 532 501 520 485 450 480 50% 55a 529 550 508 490 519 70% 584 562 580 558 540 550 90% 618 619 640 619 600 610 95% 636 - - 645 640 635 comParative ExamPle 1 ~30a~
500 grams of (Stock H as disclosed in Table 1) diesel oil was placed in a 1000 ml volume reactor which consisted of a beaker with a septum on the side. The sep-tum was about 1 inch from the bottom surface of the reactor for nitric acid injection. Mitric acid was used as the nitrogeneous treating agent. 21.4 grams of a 70% aqueous solution of nitric acid was placed in a syringe and mounted on an injection pump. This quantity of acid corresponds to an acid-to-oil weight ratio of 0.03:1 (based on 100% nitric acid). The oil was stirred with a lab size stirrer at 1000 rpm. The temperature of the reactor was controlled at 85C
throughout the treatment step with nitrlc acid. The nitric acid was injected over a 15 minute period.
After the acid injection, the reaction mixture was further stirred for an additional 60 minutes to ensure consumption of residual acid in the mixture. At the completion of the nitric acid treatment, the oil was separated rom the residue formed by simple decantation to remove any excess nitric acid. The separated oil was weighed, and filtered. A portion of the treated oil was water washed with a water-to-oil weight ratio of 0.1:1 followed by filtration.
A specified amount of the water washed oil was blended into a diesel oil pool which contained 30 ~3~ i4 volume percent o LC0, the characteristics of which are shown in Table 1. The blends were made according to the nitrogen content of the treated oil to obtain 100 ppm nitrogen added to the pool which corresponded to at least a 2 cetane number enhancement to produce a diesel ~uel blend. Samples of the ble~ded product6 were analyzed for Nalco stability and color (ASTM-D 1500).
The Nalco stability rating of this blend wa5 13 which is substantially higher than acceptable for a fungible diesel fuel. The immediate ASTM color reading for this diesel fuel blend was 1.5 which Was the same color reading a~ that of the die~el oil pool beore addition of the treated diesel oil. After 3 days storage of the blend, the ASTM color was measured to be 4.0, which is greater than a diesel fuel meeting commercial specifications of 3. The results o color testing with longer storage time are shown graphically in Figure 1.
Example 2 Another portion of the decanted treated oil obtained as discussed in Comparative Example l above was treated with a 1 M aqueous solution of sodium hydroxide with a 60dium hydroxide to oil weight ratio of 0.1:1. After the separation of the aqueous phase, the product was filtered and blended into a diesel oil pool as described in Comparative Example 1 above ~L30~
(containing 30 volume percent LC0) with a blend ratio to obtain 100 ppm nitrogen added to the diesel oil pool.
Samples of the blend were analyzed for Nalco stability and ASTM color as described above. The Nalco stability rating of this blend wa~ 3, a value generally acceptable for a commercial diesel fuel. The immediate ASTM color readin~ for this blend wa3 the same as the diesel oil pool before addition of the treated oil.
After 3 days storage, the blend ASTM color was 2 . 5 .
The resul ts o~ the color test~ With ~torage time for this blend are also shown graphically in Figure 1.
Substantial improvement in the storage color of the blend with time ca~ be seen from the results in Figure 1.
Comparative Example 2 500 grams of a diesel oil (Stock I) was treated With 21.4 g of a 70% nitric acid aqueous solution according to the procedure set forth in the Comparative Example 1. After decantation, a portion of the treated oil was water washed wlth a water-to-oil weight ratio of 0.1:1. The washing procedure was as follows: 100 g of treated oil was mixed with 10 g of water. The mixture was placed in a separatory funnel and shaken or 30 seconds. The mixture was allowed to settle for ~:~o~
10 minutes after which the two phases were separated.
The produc-t oil was then filtered. A speciied amount of the treated oil was blended into a commercially available sample of diesel oil pool which contained LCO. The percent blends were made according to the nitroqen level of the treated oil in order to obtain 100 ppm nitrogen added to the diesel oil pool.
Different level~ of Petrolite T-363 as a stability additive (a commercially available stability additive believed to be a mixture of alkyl amines and al}cyl amine iodine complexes) were added to this blend and the Nalco stabilikies were measured. The results obtained are shown graphically in Figure 2.
Example 3 Another portion of the treated oil obtained as described in Comparative Example 2 after decantation was treated with a 1 M solution of a~monium hydroxide with a weight ratio of 0.1:1 to the oil according to the procedure of Compartive Example 2. After separation of the two phases, the product was filtered and blended into a diesel oil pool as described in Comparative Example 2 above with a blend ratio to obtain 100 ppm nitrogen added to the diesel oil pool.
Different levels of Petrolite T-363 as a stability additive were added to this blend and the Nalco OOfiA
stabilities were measured. The results obtalned are shown graphically in Figure 2. Figure 2 clearly demonstrates th~ reduction in the amount of stability additive required upon alkali treatment of the treated oil after decantation to remove excess nitrogenous treating agent.
When the above procedures of Example 3 were repeated using aqueou~ solutions of sodium hydroxide or potassium hydroxide, similar re~ults were obtained.
Example 4 500 qrams of a diesel oil ~Stock H) was treated with 21.4 g o a 70% aqueous nitric acid solution according to the procedures outlined in Comparative Example 1.
The treated oil after decantation to remove excess nitrogenous treating agent was treated with aqueous solutions of different inorganic alkali compounds. The inorganic alkali compounds used were: 1 M sodium hydroxide, 1 M potassium hydroxide, 1 M ammonium hydroxide. For comparison, treatment was also conducted with a water wash. The treatments were done according to the procedure set forth in Comparative Example 2 above. The a~ueous phase from each treatment was analyzed for chemical oxygen demand (COD). The results obtained are shown in Table 4 below. The oil ~.~0~4 pha~e from the washes was filtered and the nitrogen content was measursd. Compared with the nitrogen measurements on the unwashed oil, the percent nitrogen reduction of each treatment was calculated. The results obtained are also shown in Table 4.
Table 4 % Nitrogen TreatmentCOD (mq/l) Reduction Water 11794 Sodium Hydroxide183311 20.27 Potassium Hydroxide 145984 18.70 Ammonium Hydroxide 40309 11.08 These results in the above examples demonstrate that an improvement in cetane number of a diesel fuel blend can be obtained, when the t~eated oil added to the blend is treated with a solution of an inorganic alkali and such is then blended with an untreated diesel oil. The blend so produced has good storage stability and color and possesses useful levels of Ramsbottom carbon. Further, these results show that the amount of stability additives which may be used in such blends is reduced due to the inorganic alkali treatment.
While the invention has been described in detail and with reference to specific embod~ments thereof, it Ç;4 -- ss --will be apparent to one skilled in the art that various changes or modification~ can be made therein without departing from the scope and spirit thereof.
In a further embodiment of this invention~ this invention provides a process for the enhancement of the cetane number of and improvement in color developed on storage of a non-fungible diesel fuel comprising:
(1) treating a first diesel oil with a nitrogenous treating agent in a nitrogen ~3()0~4 - ~6 -amount, equivalent on a 100% nitric acid basis, to about 10 weight percent or les~ of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent rom the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated dieseL
oil; and (4) blending the treated diesel oil of step (3) with a second diesel oil which has not been treated as in step (1) above to produce a blended diesel fuel such that the nitrogen added content in the blended diesel fuel is about 1,000 ppm or less of nitrogen added, and : ~ wherein the first diesel oil treated in step (1) and/or the second diesel oil blended in step (4) and/or the blended product o step (4) is a non-fungible diesel fuel.
BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWINGS
Figure 1 is a graph showing the relationship between ASTM color and age of the diesel fuel blend : ' produced by the process of this invention.
Eigure 2 is a graph showing the relationship between Nalco stability and amount of stability 0~4 improviny additive present in a diesel fuel blend produced by the process of this invention.
Figure 3 is a graph showing the relationship be-tween Ramsbottom carbon and nitrogen added to the diesel oil blend.
Figure 4 is a graph showing the relationship between stability and nitrogen added to the blended diesel fuel.
Figure 5 i8 a graph showing the average blending cetane numbers of blended diesel fuel products for varying amounts of treated diesel fuel in the blend.
Figure 6 is a graph showing the calculated pool cetane of blended diesel products produced.
DETAILED DESCRIPTION OE THE INVENTION
As indicated above, the process of this invention involves, in particular, enhancement of the cetane number of a diesel fuel and improvement in color developed on storage. The process basically comprises:
(1) treating a diesel oil with a nitrogenous treating agent in a nitrogen amount, e~uivalent on a 100~ nitric acid ba~is, to about 10 weight percent or less to the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (l);
(3) treating the diessl oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated oil of step (3) with a diasel oil which has not been so treated as in step (1) to produce a blended diesel fuel such that the nitrogen added content in the blended diesel fuel (a) is about 300 ppm or less of nitrogen added when the diesel oil treated in step (1) is a diesel oil obtained from virgin diesel oil s~ock, or (b) is about 450 ppm or less of nitrogen added when the diesel oil treated in step (1) is a diesel oil obtained from hydrotreated diesel oil stock.
In the first step of the process of this invention, a diesel oil is treated by contacting such with a nitrogenous treating agent in a nitrogen amount equivalent to about 10 weight percent or less on the diesel oil feed of nitric acid based on the nitrogen content of a 100% concentration nitric acid.
If desired, the feed oil can first be subjected to pretreatment, 8uch as by washing to remove phenols or other corrosive components of the oil, filtering to ~00~4 remove gum or sediment, or heating or treatment with H2S04 as conventionally used. In the fir~t step of the process of the invention, the treating agent is a nitrogenous treating agent. The term "nitrogenous treating agent" is used herein to mean any known nitrogen-containing oxidizing compound including, e.g., a gas containing at least one nitrogen oxide with more than one oxygen atom for each nitrogen atom, a liquid containing at least one nitrogen oxide with more than one oxygen atom for each nitrogen atom, nitric acid and nitrous acid.
The treating gas used can be a gas containing only such a nitrogen oxide or can be one which contains mixtures of such nitrogen oxides. Furthermore, the treating gas can be one which also contains other components such as oxygen, nitrogen, lower nitrogen oxides, i.e., nitrogen oxides containing only one oxygen atom or less than one oxygen atom per nitrogen atom in the oxide. For efficiency, preferably the treating gas will be one which contains only nitrogen oxides with more than one oxygen atom for each nitrogen atom but mixtures with other gases such as oxygen, nitrogen, as well as inert gases such as air, helium and helium with air can be employed if desired.
Suitably the treating gas will contain at least 0.5% by ~3~ i4 volume of at least one nitrogen oxide with more than one oxygen atom for each nitrogen atom, but the concentration can be reduced if the flow rate of treating agent is increased for a longer time.
Nitrogen dioxide or its dimer N204 can be advantageously employed, alone or in a admixture with air.
The nitrogenous treating liquid used can be li~uid ni-trogen oxides as defined above, nitric or nitrous acid either concentrated or in admixture with up to about 90% water by weight. Preferably the liquid nitrogenous treating agent is an a~ueous solution of nitric acid containing about 50 to 90% by weight nitric acid.
However, the above described concentrations, e.g., nitrogenous treating agent concentrations, are not limiting and are given merely for exemplification.
Basically any concentration can be used as long as the nitrogenous treating agent is present in sufficient amounts to achieve in the blended product the nitrogen added amounts for the process of the invention when the treated diesel oll is blended with the untreated diesel oil.
When liquid nitric acid is used as a nitrogenous treating agent in the present invention, it may ~3~0~
advantageou~ly be used in combination with other organic or inorganic acids. Suitable inorganic acids include sulfuric and phos~horic acids, and suitable organic acids include, e.g., acetic and formic acids.
The organic and inorganic acid may be used alone or in combination. Typically, an inorganic acid can be added to the aqueous nitric acid solution used as a trea-ting agent in an amount of fxom about 5 to 200% by weight of the nitric acid solution, and an organic acid can be added in an amount from about 5 to 200% by weight of the nitric acid æolution. Preferred combinations of nitric and au~iliary acids include nitric and sulfuric, nitric and acetic, and nitric and formic acids.
When liquid nitrous acid is used as a nitrogenous treating agent in the present invention, it may advantageously be uæed in combination with other organic or inorganic acids. Suitable inorganic acids include sulfuric and phosphoric acids, and suitable organic acids include, e.g., acetic and formic acids.
The organic and inorganic acid may be used alone or in combination. Typically, an inorganic acid can be added to the aqueous nitrouæ acid æolution used as a treating agent in an amount of from about 5 to 200% by weight of the nitrous acid ~olution, and an organic acid can be added in an amount from about 5 to 200% by weight of 1~ 0~4 the nitrou~ acid solution. Preferred combinations of nitrous and auxiliary acids include nitrous and sulfuric, nitrous and acetic, and nitrous and formic acids. Mixtures of nitric acid and nitrous acid can also be used.
In the first step o the process of this invention, a diesel oil such as atmoæpheric gas oil is reacted with a nitrogenous treating agent in the form of a liquid or gas. The contacting of the diesel oil with the treating liquid can be accompli~hed by any means conventional in the art or contacting two liquid reactants, e.g., by injecting the acid mixture under the surface of agitated oil contained in a reactor.
When a treating gas is employed, the treating gas can be contacted with the diesel oil using any conventional means for contacting a gaseous reactant with a liquid reactant. Suitable examples of such means for contacting a gaseous reactant with a liquid reactant include dispersing the gas as bubbles in the li~uid, trickling the liquid over an inert solid bed with gas passing also over the bed co-currently or countercurrently to the liquid flow, the latter type flow being preferred.
It is important in the first step of the process of thi~ invention to control the operating parameters 130~ Ei4 during the reaction of the diesel oil with the treating gas or liquid to insure that the nitrogenous treating agent is employed in a nitrogen amount e~uivalent to about 10 weight percent or less, preferably 6 weight percent or less, more preferably 5 weight percent or less, of nitric acid based on the nitrogen content of 100% nitric acid. In accordance with the process of the present invention, by conducting step (1) in this manner and in combination with steps ~2) and (3) described hereinafter, this results in a product of extremely high cetane value which may be advantageously blended into a dlesel pool without deleterious effects on Ramsbottom carbon and ~tability. This important processing control as to the reaction of the diesel oil with the nitrogenous treating agent is described in more detail below.
As used herein, the term "nitric acid e~uivalent-to-oil ratio" (acid-to-oiL ratio, A/0) refers both to the weight of water-free nitric acid to the weight of diesel oil feedstock and to the weight of undiluted gaseous or liquid nitrogenous treating agent to the weight of diesel oil feedstock, and is from about 0.0002 to 0.10, preferably from about 0.0005 to 0.05, for the acids and from 0.0002 to 0.10, preferably 0.0005 to 0.05, for the nitrogen oxides. The control 5~
of the trea-tment may be achieved by controlling the water content of the acid in the reactor, by controlling the mixture of nitrogenous gas and air or inert gas used or by controlling temperature, time and degree of agitation. The treatment can also be controlled and improved by the copresence of sul~uric acid through itF9 effect on water availability or other auxiliary acid mixed with the treating agent. This control of the amount of nitrogenous treating agent to the total weight of the diesel oil feed in step (1) can be easily maintainéd.
The reaction of the first step of the present invention can be performed at any temperature from about -40 to about 200C, or less, moet preferably from about 25 to 90~C. The reaction time is not particularly limited, and may include9 for example, any time from about 1 minute to about 3 weeks. This first step o the present invention may be conducted at atmospheric pressure or at greater or lower pressures as de~ired. Advantageously, the reaction step is conducted using conventional agitation means, such as a stirrer or such as a pumparound reactor.
Since a nitrogenous treating agent is used in the first step of the present invention, typically an increase in nitrogen compound content over that ~3~
originally present in the diesel oil will be observed.
While not desiring to be bound by theory, the reason for the increase in observed nitrogen compound content is believed to be that nitration and esterification of the diesel oil substrate can occur resulting in an increase in the heteroatom nitrogen compound content.
~ ecause of the complexity o the reactions involved, the treating agent~ may well do more than oxidize or nitrate compounds contained in the diesel oil in the process according to the invention. Hence, the first step is variously described herein as "nitrogenation" or simply "nitrogen treatment" or more simply "treatment", which refers to any reaction of the nitro~enous treating agent and diesel oil or its components, without limitation, and without reliance on any particular reaction or reaction mechanism.
Contact times on the order of less than about 120 minutes and weight ratios of nitrogenous treating agent to diesel oil feed o less than about 0.1 are desirable not only from the standpoint of efficiency hut also from the standpoint of economics. Particularly preferably, a contact time of ahout 30 minutes in combination with a weight ratio of nitrogenouæ trea-ting agent to diesel oil feed of about 0.05 or less can be o~
advantageously employed for maximum yield of diesel oil with improved ce-tane rating and useful stability.
However, because of the known :relationship of nitrogenous treating agent to cetane number, it i9 often advantageous when using a nltrogenous treating agent to carefully control the minimum amount of nitrogen compounds added to the diesel feed in order to insure a suficient cetane number in the diesel fuel produced.
Depending on the nature of the nitrogenous treating agent employed, one ~killed in the art can easily determine the amount o nitrogenous treating agent to use to ensure the proportion employed i 6 a nitrogen amount equivalent to 10 weight percent or less nitric acid based on the weight of the diesel oil fed as a eed stock in step (1) of the process of this invention.
The process of this invention is applicable to the upgrading of diesel oil which can be derived from any source, for example, a conventional petroleum crude oil or crude oil fraction containing sulfur, aromatic, olefinic and naphthenic compounds as impuritles. The term "die~el oil" as used herein is broadly deEined to include any hydrocarbon having a nominal boiling range of about 350F to 700F which can be upgraded by the 1~0~4 process o this invention to meet commercial speciications for a diesel fuel and the term "diesel fuel" is ~enerally used to describe the upgraded product, although the terms can be used interchangeably.
The process of this invention is basically not limited in term~ of the source of the diesel oil, but is applicable to any diesel oil from petroleum, coal, shale, tar sands, etc.
In the process for upgrading diesel oils accord:ing to the invention, particular product specifications may vary over a range. Based upon the disclosure contained herein, the present process may be readily applied and modified by one skilled in the art to produce a blended diesel fuel having particular desired specifica-tions, particularly with respect to the basic criteria of cetane, stability, Ramsbottom carbon and sulfur content, density and boiling range. Furthermore, the process of this invention can be employed in combination with conventional techniques for meeting product specifications as desired, e.g., by addition of chemical additives such as corrosion inhibitors, stabilizer~ and the like.
Fuel stability is measured by a number of accelerated tests, one of which is the Nalco 300F
~o~!Ei4 test. For satisfactory stabili.ty in commercial storage and use, a transportation fuel must exhibit a Nalco rating of about 7.0 or lower. A rating of about 7.0 is the upper level of acceptability for commercial use, although a lower limit is desirable. The applicable Nalco test is well known in the art, and the test can be simply performed, for example, by placing 50 ml of oil to be tested in a tube 3 cm in diameter, heating the tube in a 300F bath for 90 minutes, and then cooling the oil. The oil i~ then filtered using a micropore filter with a number 1 filter paper, the filter and the filter paper are washed with heptane, and the residue remaining is compared with standard samples to determlne the stability rating. If a fuel has a Malco rating exceeding 7, it may often be blended with other ~tocks or treatsd with economic levels of chemical additives to bring it into specificat1on.
This approach can be smployed with the blended fuel product produced by the process of this invention as well.
In addition to management of the above criteria of stability and cetane number, Ramsbottom carbon content is an important ~uality speciication for diesel fuels, since fuels high in Ramsbottom carbon cause fouling problems when used in diesel engine~. In an acceptable ~30~ 4 diesel fuel, the Ramsbottom carbon content is preferably less than about 0.3 weight per cent, as determined by the method disclosed in ASTM D 524, prior to addition of any nitrate additives for cetane improvement.
Nonfungible fuels also have commercial importance, such as dedicated uses for railroad engines and the like. In these applications, fuel specifications, for example, Ramsbottom carbon and stability can be grea-tly relaxed from those discussed above, such as permitting a Ramsbottom carbon content o, for example, about 1 to about 10%. For these cases, the present inven-tion still finds important applicabillty at appropriately elevated levels o nitrogen added.
While not desiring to be bound by theory, it is currently believed that the complex process according to the pre~ent invention for upgrading diesel oils by contact with a nitrogenous treating agent probably involves nitrogen addition to paraffins, olefins, naphthenes and aromatics to form nitrates, esters, amines, azides, indoles and the like.
As indlcated above, the process of this invention can be employed on an atmospheric gas oll fraction derived from li~uid petroleum crude sources.
Atmospheric gas oil is one component used in diesel oil ~1~31)~
blending, and may contain an off-specification sulfur content for use as a diesel fuel. Typically, ~ulfur as a heteroatom i9 present as thiol.s, di~ulfides, sulfides, thiophenes, and mercaptans, and nitrogen is present a~ substituted pyridines and pyrroles, and other compounds. A typical analy~is of atmospheric gas oils is set forth in Table 1 below.
13~
Table 1 Properties of Atmospheric Gas 0i1 (AGO) and of Liqht CYcle Oil (LC~
Stock H Stock I LCO
Gravity, API 33.1 34.2 17.65 Sulfur, wt.% 0.5 0.460.77 Nitrogen, ppm 156 191 679 Ramsbottom carbon, % 0.156 0.105 0.620 Nalco* 1 2 2 Cetane Number 46.0 41.0 22.7 D86 Distillation, F
start 290 250 430 5% 410 380 465 10% 435 395 490 30% 487 450 530 50% 517 490 550 70% 550 540 570 90% 602 600 625 95% 676 640 650 After the completion of the treatment of the diesel oil With the nitrogenous treating agent in step (1) of the process of this invention, unreacted nitrogenous treating agent is separated from the diesel * trade mark fuel in step (2). Where excess nitrogenous treating agerlt is separated, this can be achieved by decanting of the residue phase, by strippin~ of the nitrogeneous treating agent, or by other techniques well known to one skilled in the art or combinations of these physical removal techniques.
In step (3) of the process of this invention, the diesel oil from step (2) is treated with an inorganic alkali preferably an alkali metal hydroxide or a~monium hydroxide or mixtures thereof. Preferably a solution, e.g., an aqueous solution, of the inorganic alkali is employed. Where a solution is employed, a suitable concentration of alkali in the alkali solution is about 0.01 to about 5 M, more preferably 0.05 to 2.0 M, even more preferably 0.5 to 2.0 M, and most preferably 0.5 to 1.0 M. The alkali solution is used in a weight ratio to the diesel oil of step (2) of about 0.01 to l:l, preferably 0.08 to 0.5:1, most preferably 0.08 to 0.15:1.
A preferred inorganic alkali is ammonium hydroxide since it has been found, as is shown in the examples yiven hereinafter, that the chemical oxygen demand (COD) of the wash separated from the diesel oil in step (2) in treatment for environmental release or reuse is markedly reduced.
- 33 - ~
The treating of the treated diese]. oil from step (2) with the inorganic alkali can be achieved by simply mixing the diesel fuel obtained in step (2) with the alkali. Any conventional means for achieving effective contact, such as co-current or countercurrent flow or a simple addition with agita~ion, can be employed to treat in step (3) the diesel oil from step (2). Although not essential, if desired, the diesel oil of step (3) can be subjected to a water washing step prior to use of the treated diesel oil of step (3) to produce the diesel fuel blends of ~tep (4).
In the next step (4) of the process of this invention, the treated diesel fuel so obtained is then mixed with a diesel oil which has not been BO treated, herein "untreated diesel oil", to produce a blended diesel fuel.
Examples of untreated diesel oils which can be used and mixed with the treated diesel fuel obtained in step (3) include any diesel oil with a boiling range of about 350F to about 700F. While in the process of this invention, any untreated diesel oil as previously described can be blended with the treated diesel fuel obtained in Step (3) above to achieve cetane enhancement and improved color development on storage, it would be obviou~ to one skilled in the art that the ~3~ 4 properties of the untreated diesel oil to be blended must be taken into account such that when the blend product is produced, other specifications required for a commercial fuel, such as sulfur content, Ramsbot-tom carbon content, stability, and the like, are met.
In order to enhance the cetane number of the ultimate diesel fuel blend, the nitrogen content added into the blended diesel fuel comprising the mixture of the treated diesel uel and the untreated diesel oil is carefully controlled in accordance with the ollowing parameters.
SpeciEically, where the diesel oil feed to step (l) is obtained from virgin diesel oil stocks, such as atmospheric gas oil, the amount of nitrogen added into the blended diesel fuel is about 300 ppm nitrogen or less, generally 150 ppm or less, more generally 100 ppm or less..
Where the diesel oil feed to step (1) is obtained from a diesel oil from hydrotreated diesel oil stocks, such as an atmospheric gas oil treated with hydrogen in the presence of a cataly~k at a temperature exceeding about 600F and a pressure exceeding about ~00 psi, the amount of nitrogen added into the diesel fuel blend is about 450 ppm nitrogen or less, generally 300 ppm nitrogen or less, more generally 200 ppm or less. The 1~ 4 minimum amount of treated diesel oil prepared in steps (1), (2) and (3) which i~ employed in the blended product produced in step (4) is at lea~t about 5 ppm nitrogen added, whether the diesel oil ~tock treated in step (1) is from virgin diesel oil stocks or hydrotreated diesel oil stocks.
Where the blended diesel product is to be used as a nonungible fuel, i.e., where the fuel i5 produced for a specific end use and thus adherence to normal specifications of a fungible commercial diesel fuel are not of concern, then the diesel oil feed to step (1) can be any refinery stock having appropriate properties such that when subjected to the process of this invention provides blends meeting nonfungible specifications in the final product blend. In this case, the nitrogen added due to the treated diesel oil of step (3) in the blended product can be such that the diesel fuel blend contains about 1000 ppm or less of added nitrogen, generally 800 ppm or less of added nitrogen, more generally 600 ppm or less of added nitrogen Use of the treated diesel oil in the blend produced with more than the above described levels of nitrogen added to the blend results in the inability to meet the desired blended product specifications for a diesel fuel.
The diesel oil stocks used to which the present invention is applicable can vary widely, and specifically can contain initial nitrogen levels from as little as about 5 ppm up to levels of about 1000 ppm. Surprisingly, even though it is conventionally believed there is a relationship of cetane to nitrogen level of a fuel, it has now been found that as a result of this invention it is no-t the total nitrogen content of the product blend which is relevant to simultaneous control of cetane, Ramsbottom carbon, and stability of the fuel product. Without regard to the nitrogen content of the ultimate blend obtained, the amount of added nitrogen i8 the relevant parameter to be controlled. Added nitrogen is defined herein as the nitrogen content of the final blended product after step (4) less the nitrogen content of the untreated diesel oil stock used in step (4) before addition of treated diesel oil obtained from step (3).
Regarding the blendability of Ramsbo-ttom carbon content, it must be recognized that ASTM procedures reguire that the fueL first be distilled, and the carbon measurement then be made on the 10% bottoms remaining (by pyrolysis). This is because the Q~
Ramsbottom carbon precursors are normally found in the bottom cut of the die~el fuel. By concentrating these precusors by distillation, the precision of the carbon measurement is greatly improved. If another low Ramsbottom stock is blended, Ram6bottom carbon is not necessarily reduced because that blend-stock is distilled out before carbon measurement. Blending a heavier stock with the high carbon content stock ~so that the bottom 10% i~ relatively dilute in carbon-forming compounds) might be contemplated but this would violate the ASTM end point specifications on the diesel fuel. Fur~hermore, for nitrogenated stocks produced in the process of thè present invention, the nitrogen compounds are known to be polymerization catalysts for carbon formation, so that small amounts produce signiicant Ramsbottom carbon even when diluted.
As to stability of diesel fuels, the stability of diesel fuels and blends of diesel fuels are generally improved by the addition of certain stability addi-tives. Use ul additives include alkyl amines in either a petroleum or polymeric solvent. The amine functional groups in these additives are predominantly found in high molecular weight molecules containing either branched chain alkyl or allyl groups. Dupont, UOP, and 13~
Ethyl Corporation produce additive~ of this general composition, although the specific compositions of such additives are generally proprietary. sorg-warner Chemicals market~ an additive which has a phenolic base structure, while Petrolite Corporation produces an alkylamine-iodine base additive ~n an acrylate polymer and xylene solvent as stability additives to diesel fuels. Table 2 summarizes known compositional details of these commercially available additives.
It has also been found that when conventional stability additives are employed with the blended diesel fuel product produced by the process of the present invention, the levels required to achieve acceptable stability results are unexpectedly reduced.
More specifically, the Petrolite commercially available stability additive (Petrolite T-363), provided the best stability improvement response for a given stability additive level. Reduction of the ASTM
D 2274 oxidation stability rating by 47%, 67% and 81%, using stability additive levels of 60, 100 and 150 ppm (based on the blended diesel fuel product obtained in this invention) at 3% by weight of the diesel oil product of step (3) in the blend diesel fuels of step (4), re~pectively were aGhieved, with only 60 to 80 ppm being re~uired to provide an adequate stability.
1~0~
Similar stability improvements at 6tability additive levels in the 60 to 80 ppm range were also achieved wi-th other Petrolite additives and would be expected over the entire range to 150 ppm.
Although the other amine based commercially available additives, e.g., those produced by Dupont, UoP, and Ethyl improved stability, this improvement was less than that achieved with the preferred commercially available Petrolite products for the same additive level. However, acceptable stability could be achieved at a higher ppm level than for Petrolite.
A reduction in the stability additive requirement to about 25% to 75%, more typically 33% to 50%, for the blended product produced in the present invention, where the product of step (3) used to produce such blend of step (4) is subjected to the inorganic alkali treatment as in step (3) in comparison with a blended product produced where the product used in producing the blend of step (4) is not so subjected to an alkali treatment as in step (3). The inorganic alkali treatment of step (3), therefore, reduces the stability additive level re~uirement from, for example, about 60 to 80 ppm down to about 20 to 40 ppm level, to give a suitable stability based upon a product blend with a blending of 3% by weight of the diesel oil of step (3) 13(J 0~
in producing the diesel uel bl~nd of step (4) of thiæ
invention.
As a result, it can be seen that the process of this invention provides the ability to reduce the amount of stability additive to levels of about 25% to 75%, more typically 33% to about 50%, of the amount of stability additive which would be employed in the absence of the inorganic alkali treatment of step (3) of the process of this invention.
~3~ 64 Table 2 Compo~itional Summary o CommerciallY Available StabilitY Additives Additive TyPe Chemical Compo~ition Petrolite T-260 Organic amines Petrolite T-316 Organic amines Petrolite T-362 Organic amines Petrolite T-363 Alkyl amine-iodine base with acrylate polymer in xylene Petrolite T-386 Organic amines UOP Polyflo T121 N-~l-methylheptyl) ethanol amine N,N' di~alicylidene-1,2-propane-dlamine in a naphtha solvent UOP Polyflo T122 Polyamino polyol N-(l-methylheptyl) ethanol a~m:Lne N,N' disalicylidene-1,2-propane dlamine in a naphtha ~olvent UOP AID T2525 High molecular weight amine polymer and petroleum solvent UOP Polyflow T120 Similar to Polyflo T121, but without a copper deactivator.
Dupont E'uel Oil Additive $~3 Organic amine Borg Warner Ultranox 226 2,6-di-t-bukyl-4~methylphenol Borg Warner Ultranox 236 4,4'-thio-bi~(2-t-butyl-5-methylphenol) Borg Warner Ultranox 246 2,2'-methylene-bis(4-methyl-6-t-butyl phenol) Borg Warner.Ultranox 254 polymeric 2,2,4-trimethyl-1,2-dihydroguinoline Borg Warner Ultranox 256 polymeric ~3terically hindered phenol Figure 1 shows the effect of storage on the blended diesel fuel resulting from step (4) of the process of the present invention as a function of ASTM
color (D-1500) in relation to time where the treated diesel oil of step (1) is washed with water or is treated with an agueous sodium hydroxide solution. It is surpising that by using the aqueous alkali solution treatment after the treatment with nitrogenous treating agent in step (1) and separation of excess nitrogenous treating agent in step ~2) but prior to blending in step (4) results in the marked improvement in color of the blended diesel fuel on storage. This is particularly true since treatment with inorganic alkali in the form of an a~ueous solution does not appear to initially have much effect on the color of the dlesel oil obtained in step (3).
Considering the background of stability and color formation of diesel oils, the mechanisms are not well known except in general terms. It is, however, recognized that trace levels of contaminants, such as nitrogen compounds, play an important role in sediment formation, often as catalysts. They may also play a role in color development. As a result, as to stability, dilution of an unstable fuel by a stable fuel does not generally improve stability appreciably.
~3~)0~
Upon dilution by a stable uel, there are still suffi~ient quantitie~ of these initi~tors to cause stability problems. Increased color on storage may also result. As a re6uLt, the conventional method to attack stability pxoblems has been to use a range of antioxidants, with the choice of the appropriate antioxidants being selected empirically (governed by which mechanism is operative or a given stock).
Unfortunately, for nitrogenated stocks, uneconomic levels o additives have been required in the past.
It has also been found in this invention that when such stability improvqng additives are used, the amount thereof necessary in the blended diesel fuel produced by the proceæs of this invention can be markedly reduced. Thi~ effect i8 6hown in Figure 2 discussed below.
Figure 2 demonstrates that the amount of stability additive to the diesel fuel blend obtained in step (4) of the process o this invention can be markedly reduced by using the treatment with inorganic alkali of step (3) of the process of this invention. For example, the amount of additive, Petrolite T-363 in (ppm) to achieve a particular Nalco stability for the alkali treatment using an aqueous solution of ammonium hydroxide is markedly reduced in comparison with the ~L300~
amount of additive required for the same Nalco s-tability where the treatment in step (3) of the process of this invention i~ simply a water wash.
Figures 3, 4, 5 and 6 clearly show graphically the above advantages of the process of thi~ invention in terms of cetane enhancement and stability of the blended fuel product obtained in accordance with the trea-tment with nitrogenous treating agent step, the removal of excess nitrogeneous treating agent step and the blending step as disclosed in parent application Serial No. 832,196, iled February 24, 1986, the disclosure of which is incorporated herein by reference. The addition o the alkali treatment step between separation of the nitrogeneous treating agent step and the blending step as in this invention does not substantially change the nature of the improvements in cetane number enhancement achieved but additionally provides the ability to unexpectedly minimize color development of the diesel fuel blend as shown in Figure 1 and reduce the amount of any affirmatively added stability enhancer which might be used as shown in Figure 2. As long as the nitrogen added levels adhered to set forth in step (4) above are as to the relationship of the amount of treated diesel oil o step (3), used in the blend of step (4~, the same 136~ 4 general cetane enhancements achieved in the process of said parent application Serial No. 832 J 196 are achieved with the process of this invention and surprisingly the amount of color developed on storage of the blend of step (4) i5 minimized as shown in Figure 1 hereof. The presence or absence of an alkali treatment step does not substantially affect the cetane enhancement, characteristics achievable, etc.
To illustrate the cetane enhancement, stability, etc., characteri#tics achievable in the process of this invention, reference more specifically is made to Figures 3 to 6 below~
To obtain the data shown in Figures 3 and 4, the diesel oil of step (2) was blended with an untreated oil to produce a blend product. Since the oil of step (2) contained nitrogen at levels of 2000 to 4000 ppm, the this oil was employed in the blend at about 2% to 15% by weight of the total blend. Analogous results to those shown in Figures 3 and 4 are achieved when an alkali treated oil of step ~3) is used to produce a blend product. The prior art has variously reported cetane number improvements of 5 to 20 numbers. Figure shows blending cetane number~ achieved generally corresponding to data with less than about 15% by weight treated oil in the blend. Since the di~sel oil 130~4 feed had a cetane number of about 40, the product oil of step (2) or of step (3) would be e~pected to have a cetane number o~ 45 to 60. Quite aurprisingly, cetane numbers of 60 to 220 are achieved when blend proportions of lesa than 15% by weight of the oil obtained in step (2) or in step (3) are used in producing the diesel fuel blend product. However, it is to be emphasized the blend proportion used in Eigure was employed only for purposes of illustration.
Various other combinations of treating reactor variables and blend proportions to provide appropriate levels of added nitrogen as herein defined can be employed.
As will be discussed below, the line through the data of Figure 5 may be used to describe the cetane number of oils produced in step ~2) and by analogy in step (3) of the present invention. For these runs, this corresponds to blend proportions of less than 15%
by weight. When the cetane of the final blend of diesel fuel obtained is calculated from the curve shown in Figure 5 to eliminate scatter, the resulta of Figure 6 are obtained. In view of the very ~mall amounts of step (2) and by analogy of step (3) oil used, it is very surprising that a large improvement in cetane of the blended diesel fuel product is achieved.
0~;4 In particular, a 3 cakane number increase in the diesel fuel hlend produced is obtained. Furthermore, it is particularly surprislng that the maximum in the cetane curve resides in the blend region where Ramsbottom carbon content and stability are simultaneously controlled.
Figures 1 through 6 indicate surprising and unobvious results, particularly by considering the weight of the combination o these effects. It is surprising that blends with added nitrogen having acceptable Ramsbottom carbon also provide blends of acceptable stability, with large cetane improvement and with a maximum cetane in regions of excellent stability and Ramsbottom carbon as well as improved blend color development on storage, i.e., less color developed, as discussed above.
The treated diesel oil from step (1) of the process of this invention can typically contain from 2000 to 4000 ppm nitrogen. The measured cetane ratings of such treated oils generally is 44 to 50 with an initial cetane rating of 40 for the diesel oil feed to step (1), with an improvement over step (1) diesel oil feed (40 cetane) of 4 to 10 cetane numbers, similar to that which would be expected rom the prior art. If the nitrogen added data are considered for an untreated ~3~)0~)~4 - 4~
feed o 100 ppm nitrogen to produce the diesel uel blend, simple calculations reveal that less than about 20% by weight and usually less than about 10% by weight of treated diesel oil can be accommodatled in the blend.
With such a low blend percentage o treated diesel oil, it would not be expected that the blended diesel fuel product could have a cetane improvement beyond about 1 number ba~ed on conventional knowledge. Nevertheless, a surprisingly large cetane improvement was obtained.
Further, if the cetane i8 measured of the blended diesel fuel product, the blending cetane value of the step (2) and by analogy of step (3) diesel oil can be back-calculated from the well-known linear blending equation. The surprisingly large cetane improvement of the diesel fuel blend produced leads to extremely large apparent blending cetane ratings for the diesel oil product obtained from step (2) or step ~3). Whereas conventionally, cetane improvements of the die~el oil product of steps (1), (2) and (3) of about 10 cetane numbers might be predicted and such valu~s were indeed measured for pure diesel oil product of step ll), the blending cetane values of the diesel oil product obtained after conducting steps (1), (2) and (3) are markedly increased.
~ 3(~0~Ç~4 With these dilute dies~l blends, little cetane improvement would have been expected. However, as shown in Figure 5, the effective cetane rating of the diesel oil product used in the blend produced becomes surprisingly large for the~e dilute blend~. Not only do these blends exhibit useful Ramsbottom carbon and stability under the nitrogen added criteria of the present invention, but a~so the cetane level of the diesel fuel blend i8 maximized as shown in Figure 6.
The blended diesel fuel obtained in accordance Wit}l the process of this invention can be used in any application wherein a diesel fuel meeting commercial specifications is desired. For example, the blended diesel fuel can be used as fuel for automotive, motor truck, railroad or marine diesel uses.
The following examples are given to illustrate the process of this invention in greater detail. ~owever, these examples are not to be construed as limiting the scope of the present invention but rather are given to merely illustrate the present invention. Unless otherwise indicated herein, all parts, percents, ratios and the like are by weight.
Example 1 To provide the data of Figures 3 through 6, diesel oils were fed to a treating reactor, consisting of individual stocks selected from those shown in Table 2 for each run~ These products were decanted to separate a re~idu~ phase a~ discussed below to produce a treated diesel oil. This oil was then blended with individual stocks A, B, or C selected from those described in Table 3 shown below to produce a blended diesel fuel.
The designations in Figure 3 show the nontreated diesel fuel used to blend with the treated diesel oil. Note that the treating reactor die~el oil feed, ~tocks A
through G of Table 3, contained widely varying amounts of nitrogen.
In each one o the runs, about 500 grams o diesel oil was placed in a 1000 ml volume reactor which consisted of a beaker with a septum on the side.
Nitric acid was used as the nitrogenous treating agent.
The septum was about 1 inch from the bottom surface of the reactor for nitric acid injection. A measured ~uantity of 90% nitric acid (5.5g for 0.01 A/0, 16.5g for 0.03 A/0, 2.75 for 0.05 A/0, and 33g for 0.06 A/0) was placed in a syringe and mounted on an in~ection pump. Here, A/0 designates the acid to oil weight ratio used. The oil was stirred with a lab size stirrer at 1000 RPM. The temperature o the mixture was controlled at specific levels between 25C and 80C
for these runs. Acid was injected over a 30 minute ~3003~
period. After the acid injection, the reaction mixture was further stirred for an additional 30 minutes to ensure consumption of residual acid in the mixture. A-t the completion of the treatment, the oil was separated from the residue formed by simple decantation. The separated oil was weighed~ water washed and filtered.
A specified amo~nt of oil was blended with one of the untreated diesel oils shown in Table 3. Depending on the A/0 ratio and treatment temperature used, different percent blends were made to be able to generate the relationships among variables shown in Eigures 3 to 5.
Samples of the blended products were analyzed for cetane number (ASTM D613), Ramsbottom carbon (ASTM
D524~, and Nalco stability. With 0.01 A/0 ratio usually the nitrogen content of the treated oil is about 1500 to 2000 ppm; with A/0 = 0.03 the nitrogen content of the treated oil is about 3000 to 4000 ppm and for A/0 = 0.05 the nitrogen content of treated oil is about 5000 to 6000 ppm. With A/0 = 0.01, 5 to 10 percent blends were made (N added = 75 - 150 ppm).
With A/0 = 0.03, 3 to 5 percent blends were made (N
added = 100 - 150 ppm) and with A/0 = 0.06, 1 to 2 percent blends were made (N added ~ 60 - 120 ppm) The results obtained are shown graphically in Figures 3 -to 5.
~OO~
Tablo 3 Propertles of VariouJ Dlesel Oil 5tot:ks Low Pressure ~loderate Pre3sure Ill~h Pre3~uro Strai~ht Run Dle~el _ydrotreated ~59~ Hydrotreated E F ~; C_ A B D
Gravity,API 34.637.6 32.4 38.8 36.3 34.2 30.8 Sul~ur, wt% 1.070.72 1.08 0.09 0.60 0.46 0.0 Nitrogen ~ ppm200 150 93 96 191 256 87 llam~bottom t~arbon % O.IZ90.144 0.139 0.122 0.111 0.105 0.107 N~lt70 - - 2 4 1 2 2 Cetane Number 58 53 48 39.2 41.7 41 38.8 D86 D1stlllat1On, F
Start216 300 270 405 Z50 380 5% 418 408 440 41~ 380 410 10% 4~12 446 468 440 395 426 30% 532 501 520 485 450 480 50% 55a 529 550 508 490 519 70% 584 562 580 558 540 550 90% 618 619 640 619 600 610 95% 636 - - 645 640 635 comParative ExamPle 1 ~30a~
500 grams of (Stock H as disclosed in Table 1) diesel oil was placed in a 1000 ml volume reactor which consisted of a beaker with a septum on the side. The sep-tum was about 1 inch from the bottom surface of the reactor for nitric acid injection. Mitric acid was used as the nitrogeneous treating agent. 21.4 grams of a 70% aqueous solution of nitric acid was placed in a syringe and mounted on an injection pump. This quantity of acid corresponds to an acid-to-oil weight ratio of 0.03:1 (based on 100% nitric acid). The oil was stirred with a lab size stirrer at 1000 rpm. The temperature of the reactor was controlled at 85C
throughout the treatment step with nitrlc acid. The nitric acid was injected over a 15 minute period.
After the acid injection, the reaction mixture was further stirred for an additional 60 minutes to ensure consumption of residual acid in the mixture. At the completion of the nitric acid treatment, the oil was separated rom the residue formed by simple decantation to remove any excess nitric acid. The separated oil was weighed, and filtered. A portion of the treated oil was water washed with a water-to-oil weight ratio of 0.1:1 followed by filtration.
A specified amount of the water washed oil was blended into a diesel oil pool which contained 30 ~3~ i4 volume percent o LC0, the characteristics of which are shown in Table 1. The blends were made according to the nitrogen content of the treated oil to obtain 100 ppm nitrogen added to the pool which corresponded to at least a 2 cetane number enhancement to produce a diesel ~uel blend. Samples of the ble~ded product6 were analyzed for Nalco stability and color (ASTM-D 1500).
The Nalco stability rating of this blend wa5 13 which is substantially higher than acceptable for a fungible diesel fuel. The immediate ASTM color reading for this diesel fuel blend was 1.5 which Was the same color reading a~ that of the die~el oil pool beore addition of the treated diesel oil. After 3 days storage of the blend, the ASTM color was measured to be 4.0, which is greater than a diesel fuel meeting commercial specifications of 3. The results o color testing with longer storage time are shown graphically in Figure 1.
Example 2 Another portion of the decanted treated oil obtained as discussed in Comparative Example l above was treated with a 1 M aqueous solution of sodium hydroxide with a 60dium hydroxide to oil weight ratio of 0.1:1. After the separation of the aqueous phase, the product was filtered and blended into a diesel oil pool as described in Comparative Example 1 above ~L30~
(containing 30 volume percent LC0) with a blend ratio to obtain 100 ppm nitrogen added to the diesel oil pool.
Samples of the blend were analyzed for Nalco stability and ASTM color as described above. The Nalco stability rating of this blend wa~ 3, a value generally acceptable for a commercial diesel fuel. The immediate ASTM color readin~ for this blend wa3 the same as the diesel oil pool before addition of the treated oil.
After 3 days storage, the blend ASTM color was 2 . 5 .
The resul ts o~ the color test~ With ~torage time for this blend are also shown graphically in Figure 1.
Substantial improvement in the storage color of the blend with time ca~ be seen from the results in Figure 1.
Comparative Example 2 500 grams of a diesel oil (Stock I) was treated With 21.4 g of a 70% nitric acid aqueous solution according to the procedure set forth in the Comparative Example 1. After decantation, a portion of the treated oil was water washed wlth a water-to-oil weight ratio of 0.1:1. The washing procedure was as follows: 100 g of treated oil was mixed with 10 g of water. The mixture was placed in a separatory funnel and shaken or 30 seconds. The mixture was allowed to settle for ~:~o~
10 minutes after which the two phases were separated.
The produc-t oil was then filtered. A speciied amount of the treated oil was blended into a commercially available sample of diesel oil pool which contained LCO. The percent blends were made according to the nitroqen level of the treated oil in order to obtain 100 ppm nitrogen added to the diesel oil pool.
Different level~ of Petrolite T-363 as a stability additive (a commercially available stability additive believed to be a mixture of alkyl amines and al}cyl amine iodine complexes) were added to this blend and the Nalco stabilikies were measured. The results obtained are shown graphically in Figure 2.
Example 3 Another portion of the treated oil obtained as described in Comparative Example 2 after decantation was treated with a 1 M solution of a~monium hydroxide with a weight ratio of 0.1:1 to the oil according to the procedure of Compartive Example 2. After separation of the two phases, the product was filtered and blended into a diesel oil pool as described in Comparative Example 2 above with a blend ratio to obtain 100 ppm nitrogen added to the diesel oil pool.
Different levels of Petrolite T-363 as a stability additive were added to this blend and the Nalco OOfiA
stabilities were measured. The results obtalned are shown graphically in Figure 2. Figure 2 clearly demonstrates th~ reduction in the amount of stability additive required upon alkali treatment of the treated oil after decantation to remove excess nitrogenous treating agent.
When the above procedures of Example 3 were repeated using aqueou~ solutions of sodium hydroxide or potassium hydroxide, similar re~ults were obtained.
Example 4 500 qrams of a diesel oil ~Stock H) was treated with 21.4 g o a 70% aqueous nitric acid solution according to the procedures outlined in Comparative Example 1.
The treated oil after decantation to remove excess nitrogenous treating agent was treated with aqueous solutions of different inorganic alkali compounds. The inorganic alkali compounds used were: 1 M sodium hydroxide, 1 M potassium hydroxide, 1 M ammonium hydroxide. For comparison, treatment was also conducted with a water wash. The treatments were done according to the procedure set forth in Comparative Example 2 above. The a~ueous phase from each treatment was analyzed for chemical oxygen demand (COD). The results obtained are shown in Table 4 below. The oil ~.~0~4 pha~e from the washes was filtered and the nitrogen content was measursd. Compared with the nitrogen measurements on the unwashed oil, the percent nitrogen reduction of each treatment was calculated. The results obtained are also shown in Table 4.
Table 4 % Nitrogen TreatmentCOD (mq/l) Reduction Water 11794 Sodium Hydroxide183311 20.27 Potassium Hydroxide 145984 18.70 Ammonium Hydroxide 40309 11.08 These results in the above examples demonstrate that an improvement in cetane number of a diesel fuel blend can be obtained, when the t~eated oil added to the blend is treated with a solution of an inorganic alkali and such is then blended with an untreated diesel oil. The blend so produced has good storage stability and color and possesses useful levels of Ramsbottom carbon. Further, these results show that the amount of stability additives which may be used in such blends is reduced due to the inorganic alkali treatment.
While the invention has been described in detail and with reference to specific embod~ments thereof, it Ç;4 -- ss --will be apparent to one skilled in the art that various changes or modification~ can be made therein without departing from the scope and spirit thereof.
Claims (58)
1. A process for enhancement of the cetane number of a diesel fuel comprising:
(1) treating a diesel oil with a nitrogenous treating agent in a nitrogen amount, equivalent on a 100% nitric acid basis, of about 10 weight percent or less of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated diesel oil of step, (3) with an untreated diesel oil which has not been treated as in step (1) above to produce a blended diesel fuel such that the added nitrogen content in the blended diesel fuel is (a) about 300 ppm or less nitrogen added when the diesel oil treated in step (1) is obtained from virgin diesel oil stock; or (b) about 450 ppm or less nitrogen added when the diesel oil treated in step (1) is obtained from hydrotreated diesel oil stock.
(1) treating a diesel oil with a nitrogenous treating agent in a nitrogen amount, equivalent on a 100% nitric acid basis, of about 10 weight percent or less of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated diesel oil of step, (3) with an untreated diesel oil which has not been treated as in step (1) above to produce a blended diesel fuel such that the added nitrogen content in the blended diesel fuel is (a) about 300 ppm or less nitrogen added when the diesel oil treated in step (1) is obtained from virgin diesel oil stock; or (b) about 450 ppm or less nitrogen added when the diesel oil treated in step (1) is obtained from hydrotreated diesel oil stock.
2. The process of claim 1, wherein said nitrogenous treating agent is a gaseous nitrogenous treating agent.
3. The process of claim 1, wherein said nitrogenous treating agent is a liquid nitrogenous treating agent.
4. The process of claim 2, wherein said gaseous nitrogenous treating agent is NO2 or N2O4.
5. The process of claim 31 wherein said liquid nitrogenous treating agent is an aqueous solution of nitric acid.
6. The process of claim 5, wherein the nitric acid is an aqueous solution of nitric acid containing up to about 90% by weight water.
7. The process of claim 3, wherein the liquid nitrogenous treating agent is liquid NO2 or N2O4.
8. The process of claim 1, wherein the inorganic alkali is sodium hydroxide, potassium hydroxide or ammonium hydroxide.
9. The process of claim 1, wherein the inorganic alkali is ammonium hydroxide.
10. The process of claim 1, wherein the inorganic alkali is an aqueous solution of a concentration of about 0.01 to about 5 M inorganic alkali.
11. The process of claim 1, wherein the inorganic alkali is an aqueous solution of a concentration of about 0.05 to about 2 M inorganic alkali.
12. The process of claim 1, wherein the alkali is an aqueous solution of a concentration of about 0.5 to about 2 M inorganic alkali.
13. The process of claim 1, wherein the alkali is an aqueous solution of a concentration of about 0.5 to about 1 M inorganic alkali.
14. The process of claim 1, wherein the weight ratio of inorganic alkali to diesel oil of step (2) is about 0.01:1 to about 1:1.
15. The process of claim 1, wherein the weight ratio of inorganic alkali to diesel oil of step (2) is about 0.08:1 to about 0.5:1.
16. The process of claim 1, wherein the weight ratio of inorganic alkali to diesel oil of step (2) is about 0.08:1 to about 0.15:1.
17. The process of claim 1, wherein said treatment step (1) is conducted in the presence of an organic acid.
18. The process of Claim 17, wherein said organic acid is acetic acid or formic acid.
19. The process of claim 1, wherein said treatment step (1) is conducted in the presence of an inorganic acid.
20. The process of claim 19, wherein said inorganic acid is sulfuric acid or phosphoric acid.
21. The process of claim 1, wherein the weight ratio of said nitrogenous treating agent, in an amount equivalent on a 100% HNO3 basis, to said diesel oil feed of step (1) is about 0.0002:1 to about 0.1:1.
22. The process of claim 1, wherein the weight ratio of said nitrogenous treating agent, in an amount equivalent on a 190% HNO3 basis, to said diesel oil feed of step (1), is about 0.0005:1 to about 0.05:1.
23. The process of claim 1, wherein the separating of unreacted nitrogenous treating agent in step (2) is by decanting.
24. The process of claim 1, wherein the separating of the unreacted nitrogenous treating agent in step (2) is by stripping.
25. The process of claim 1, wherein said process includes water washing the treated diesel oil of step (3) prior to blending the treated diesel oil of step (3) with untreated diesel oil in step (4).
26. The process of claim 1, wherein said process includes blending a stability additive with said blended fuel obtained in step (4) to achieve a particular level of stability and the amount of stability additive blended is about 25% to about 75% of the amount of stability additive necessary to be blended with a diesel fuel blend obtained by producing a diesel fuel blend by conducting only steps (1), (2) and (4) of claim 1 and achieve substantially said particular level of stability.
27. The process of claim 26, wherein the amount of stability additive blended is about 33% to about 50%.
28. The process of claim 1, wherein said blended diesel fuel obtained is a fuel meeting specifications for automotive diesel use.
29. The process of claim 1, wherein said blended diesel fuel obtained is a fuel meeting specifications for railroad diesel use.
30. The process of claim , wherein said blended diesel fuel obtained is a fuel meeting specifications for motor truck diesel use.
31. The process of claim 1, wherein said blended diesel fuel obtained is a fuel meeting specifications for marine diesel use.
32. A process for the enhancement of the cetane number of a non-fungible diesel fuel comprising (1) treating a first diesel oil with a nitrogenous treating agent in a nitrogen amount, equivalent on a 100% nitric acid basis, of about 10 weight percent or less of the diesel oil feed;
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated diesel oil of step (3) with a second diesel oil which has not been treated as in step (1) above to produce a blended diesel fuel such that the added nitrogen content in the blended diesel fuel is about 1000 ppm or less, and wherein the first diesel oil treated in step (1) and/or the second diesel oil blended in step (4) and/or the blended product of step (4) is a non-fungible diesel fuel.
(2) separating unreacted nitrogenous treating agent from the diesel oil of step (1);
(3) treating the diesel oil of step (2) with an inorganic alkali to produce a treated diesel oil; and (4) blending the treated diesel oil of step (3) with a second diesel oil which has not been treated as in step (1) above to produce a blended diesel fuel such that the added nitrogen content in the blended diesel fuel is about 1000 ppm or less, and wherein the first diesel oil treated in step (1) and/or the second diesel oil blended in step (4) and/or the blended product of step (4) is a non-fungible diesel fuel.
33. The process of claim 32, wherein said nitrogenous treating agent is a gaseous nitrogenous treating agent.
34. The process of claim 32, wherein said nitrogenous treating agent is a liquid nitrogenous treating agent.
35. The process of claim 33, wherein said gaseous nitrogenous treating agent is NO2 or N2O4.
36. The process of claim 34, wherein said liquid nitrogenous treating agent is an aqueous solution of nitric acid.
37. The process of claim 36, wherein the nitric acid is an aqueous solution of nitric acid containing up to about 90% by weight water.
38. The process of claim 34, wherein said liquid nitrogeneous treating agent is liquid NO2 or N2O4.
39. The process of claim 32, wherein the inorganic alkali is sodium hydroxide, potassium hydroxide or ammonium hydroxide.
40. The process of claim 32, wherein the inorganic alkali is ammonium hydroxide.
41. The process of claim 32, wherein the inorganic alkali is an aqueous solution of a concentration of about 0.01 to about 5 molar inorganic alkali.
42. The process of claim 32, wherein the alkali is an aqueous solution of a concentration of about 0.05 to about 2 molar inorganic alkali.
43. The process of claim 32, wherein the inorganic alkali is an aqueous solution of a concentration of about 0.5 to about 2 molar inorganic alkali.
44. The process of claim 32, wherein the alkali is an aqueous solution of a concentration of about 0.5 to about lM inorganic alkali.
45. The process of claim 32, wherein the weight ratio of inorganic alkali to diesel oil of step (2) is about 0.01:1 to about 1:1.
46. The process of claim 32, wherein the weight ratio of inorganic alkali to diesel oil of step (2) is about 0.08:1 to about 0.5:1.
47. The process of claim 32, wherein the weight ratio of inorganic alkali to diesel oil of step (2) is about 0.08:1 to about 0.15:1.
48. The process of claim 32, wherein said treatment step (1) is conducted in the presence of an organic acid.
49. The process of claim 48, wherein said organic acid is acetic acid or formic acid.
50. The process of claim 32, wherein said treatment step (1) is conducted in the presence of an inorganic acid.
51. The process of claim 50, wherein said inorganic acid is sulfuric acid or phosphoric acid.
52. The process of claim 32, wherein the weight ratio of said nitrogenous treating agent to said diesel oil feed of step (1), in an amount equivalent on a 100%
HNO3 basis, of about 0.0002:1 to about 0.1:1.
HNO3 basis, of about 0.0002:1 to about 0.1:1.
53. The process of claim 32, wherein the weight ratio of said nitrogenous treating agent to said diesel oil feed of step (1), in an amount of nitrogenous treating agent equivalent on a 100% HNO3 basis, ratio of about 0.0005:1 to about 0.05:1.
54. The process of claim 32, wherein the separating of unreacted nitrogenous treating agent is by decanting.
55. The process of claim 32, wherein the separating of unreacted nitrogenous treating agent is by stripping.
56. The process of claim 32, wherein said process includes water washing the treated diesel oil of step (3) prior to blending the treated diesel oil of step (3) with untreated diesel oil in step (4).
57. The process of claim 32, wherein said process includes blending a stability additive with said blended fuel obtained in step (4) to achieve a particular level of stability and the amount of stability additive blended is about 25% to about 75% of the amount of stability additive necessary to be blended with a diesel fuel blend obtained by producing a diesel fuel blend by conducting only steps (1), (2) and (4) of claim 32 and achieve substantially said particular level of stability.
58. The process of claim 57, wherein the amount of stability additive blended is about 33% to about 50%.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US012,466 | 1987-02-09 | ||
| US07/012,466 US4711713A (en) | 1986-02-24 | 1987-02-09 | Process for enhancing the cetane number and color of diesel fuel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1300064C true CA1300064C (en) | 1992-05-05 |
Family
ID=21755104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000558370A Expired - Fee Related CA1300064C (en) | 1987-02-09 | 1988-02-08 | Process for enhancing the cetane number and color of diesel fuel |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA1300064C (en) |
-
1988
- 1988-02-08 CA CA000558370A patent/CA1300064C/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4746420A (en) | Process for upgrading diesel oils | |
| Tam et al. | Desulfurization of fuel oil by oxidation and extraction. 1. Enhancement of extraction oil yield | |
| Frankenfeld et al. | Storage stability of synfuels from oil shale. 1. General features of sediment formation in model fuel systems | |
| CA1278920C (en) | Process for enhancing the centane number of diesel fuel | |
| US4756819A (en) | Process for the thermal treatment of hydrocarbon charges in the presence of additives which reduce coke formation | |
| US4711713A (en) | Process for enhancing the cetane number and color of diesel fuel | |
| US3095368A (en) | Process for removing metallic contaminants from oils | |
| US4464251A (en) | Removal of contaminants from organic compositions | |
| EP0236021A2 (en) | Process for upgrading diesel oils | |
| CA2077682A1 (en) | Fuel oil compositions | |
| CA1300064C (en) | Process for enhancing the cetane number and color of diesel fuel | |
| US4465589A (en) | Removal of contaminants from organic compositions | |
| US3309309A (en) | Denitrification of hydrocarbons | |
| EP1713885B1 (en) | Hydrocarbons having reduced levels of mercaptans and method and composition useful for preparing same | |
| US2731393A (en) | Desulfurization and sweetening process | |
| US3052626A (en) | Treatment of petroleum products | |
| US2043254A (en) | Treatment of hydrocarbon oil | |
| US3326798A (en) | Denitrification with cupric chloride and an alcohol | |
| US2013083A (en) | Process of producing a colorless doctor sweet gasoline | |
| US2318710A (en) | Gum inhibitor | |
| US2769764A (en) | Method for producing napthas of improved characteristics from highly refined naphthas by treating the highly refined naphthas with a copper acetate | |
| US1885524A (en) | Process for treating hydrocarbon oils | |
| US3013964A (en) | Treatment of petroleum products | |
| JPH10503792A (en) | Crude oil refinery process stream and / or method for reducing the sulfur content of crude oil | |
| US3013963A (en) | Treatment of petroleum products |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed |