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US3083244A - Non-catalytic process for the recovery of alkylnaphthalenes in the presence of hydrogen - Google Patents

Non-catalytic process for the recovery of alkylnaphthalenes in the presence of hydrogen Download PDF

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Publication number
US3083244A
US3083244A US750082A US75008258A US3083244A US 3083244 A US3083244 A US 3083244A US 750082 A US750082 A US 750082A US 75008258 A US75008258 A US 75008258A US 3083244 A US3083244 A US 3083244A
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Prior art keywords
alkylnaphthalenes
hydrogen
recovery
partial pressure
hydrocarbon
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US750082A
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Robert A Sanford
Henry D Ballard
Arvin D Anderson
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Sinclair Research Inc
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Sinclair Research Inc
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C15/00Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
    • C07C15/20Polycyclic condensed hydrocarbons
    • C07C15/24Polycyclic condensed hydrocarbons containing two rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G47/00Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
    • C10G47/22Non-catalytic cracking in the presence of hydrogen

Definitions

  • This invention relates to a process for recovering alkylnaphthalenes of high purity and particularly pertains to a thermal process conducted in the presence of hydrogen for recovering alkylnaphthalenes of high purity from petroleum hydrocarbon materials containing these and other components.
  • Alkylnaphthalenes are valuable intermediates for the production of organic chemicals since, for instance, they can be oxidized, sulfonated or dealkylated.
  • naphthalene could be produced-by catalytic processing of alkylnaphthalene containing petroleum hydrocarbon materials in the presence of hydrogen.
  • the recovery of alkylnaphthalenes from the products of these reactions has been suggested.
  • the feedstocks usually include naphthalene, alkylnaphthalenes and other materials boiling in the alkylnaphthalene boiling range.
  • naphthalene and alkylnaphthalenes can be separated using, for instance, distillation means, the other materials boiling in the alkylnaphthalene boiling range are difficult to remove without converting some of the alkylnaphthalenes to naphthalene.
  • the contact time is generally from about 0.5 to 200 and preferably from about 3 to 60 seconds.
  • R temperature in degrees Rankine X, hereinafter referred to as X value, must be between about l-l00, preferably between 2-50.
  • thermal conversion systems can be used such as, for instance, coil-type heaters, void reactors, or reactors packed with inert material, either fixed or "ice moving. Reaction systems in which any part of the products are recycled for further conversion may be used.
  • the petroleum hydrocarbon feed materials employed in our process boil primarily in a temperature range from about 300 to 800 F., preferably in :a temperature range from about 450 to 600 F., and include petroleum materials such as cracked petroleum fractions and straight run materials containing naphthenes, paraflins, aromatics and olefins in the same boiling range, as well as alkyl naphthalenes.
  • the hydrocarbon feed material includes at least about 20 weight percent and preferably about 35 to weight percent of alkyl naphthalenes.
  • the feed preferably should contain only minor amounts of biphenyl and alkylbiphenyls, fluorine and alkylfluorenes. These compounds appear to react only slowly under conditions of this process and, therefore, would have to be separated by other methods.
  • alkylnaphthalenes susceptible of recovery in the above-described hydrocarbon materials correspond to the following general formula:
  • n is 1 to 8 and R is an alkyl radical containing generally from about 1 to 13 and preferably from about 1 to 5 carbon atoms.
  • the total number of carbon atoms in alkyl groups attached to the naphthalene nucleus is generally from about 1 to'13 and preferably from about 1 to 5.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

United States Patent NON-CATALYTiC PROCESS FOR THE RECOVERY OF ALKYLNAPHTHALENES IN THE PRESENCE OF HYDROGEN Robert A. Sanford, Homewood, Henry D. Ballard, Harvey, and Arvin D. Anderson, South Chicago Heights, 111., assignors, by mesne assignments, to Sinclair Research, Inc., New York, N.Y., a corporation of Delaware No Drawing. Filed July 22, 1958, Ser. No. 750,082
4 Claims. (Cl. 260-674) This invention relates to a process for recovering alkylnaphthalenes of high purity and particularly pertains to a thermal process conducted in the presence of hydrogen for recovering alkylnaphthalenes of high purity from petroleum hydrocarbon materials containing these and other components. Alkylnaphthalenes are valuable intermediates for the production of organic chemicals since, for instance, they can be oxidized, sulfonated or dealkylated.
It has been recognized for some time that naphthalene could be produced-by catalytic processing of alkylnaphthalene containing petroleum hydrocarbon materials in the presence of hydrogen. The recovery of alkylnaphthalenes from the products of these reactions has been suggested. In these processes, the feedstocks usually include naphthalene, alkylnaphthalenes and other materials boiling in the alkylnaphthalene boiling range. Although naphthalene and alkylnaphthalenes can be separated using, for instance, distillation means, the other materials boiling in the alkylnaphthalene boiling range are difficult to remove without converting some of the alkylnaphthalenes to naphthalene. This converting, obviously, will result in lower yields of alkylnaphthalenes. However, when following our thermal process which is conducted in the presence of hydrogen, petroleum hydrocarbon materials containing alkylnaphthalenes, naphthalene, and other materials boiling in the alkylnaphthalene boiling range are converted to fractions rich in alkylnaphthalenes without excessive conversion to naphthalene.
In the process of the present invention, alkylnaphthalenes of high purity are recovered from petroleum hydrocarbon materials under conditions including temperatures generally from about 1100 to 1350 F. and, preferably from about 1140" to 1220 F.; a hydrocarbon feed partial pressure generally from about 20 to 200 p.s.i.a and preferably from about 60 to 125 p.s.i.a.; and a hydrogen partial pressure generally greater than 200 p.s.i.a. and preferably greater than 500 p.s.i.=a. and up to about 1000 p.s.i.a. The contact time is generally from about 0.5 to 200 and preferably from about 3 to 60 seconds. These conditions are employed in a relationship according to the formula tP 33.4 P l: gg 26.00)]
t=contact time in seconds P -=parti-al pressure of hydrogen in p.-s.i.
P I=partiaI pressure of hydrocarbon feed in p.s.i.
e=the base of natural logarithms ('=2.7l8
R=temperature in degrees Rankine X, hereinafter referred to as X value, must be between about l-l00, preferably between 2-50.
Various types of thermal conversion systems can be used such as, for instance, coil-type heaters, void reactors, or reactors packed with inert material, either fixed or "ice moving. Reaction systems in which any part of the products are recycled for further conversion may be used.
The petroleum hydrocarbon feed materials employed in our process boil primarily in a temperature range from about 300 to 800 F., preferably in :a temperature range from about 450 to 600 F., and include petroleum materials such as cracked petroleum fractions and straight run materials containing naphthenes, paraflins, aromatics and olefins in the same boiling range, as well as alkyl naphthalenes. Generally the hydrocarbon feed material includes at least about 20 weight percent and preferably about 35 to weight percent of alkyl naphthalenes.
In addition the feed preferably should contain only minor amounts of biphenyl and alkylbiphenyls, fluorine and alkylfluorenes. These compounds appear to react only slowly under conditions of this process and, therefore, would have to be separated by other methods.
In some operations it may be desirable to fractionate the feedstock to maximize alkylnaphthalenes'of :a particular molecular weight range. In a second type of operation severity could be adjusted to maximize alkylnaphthalenes of \a particular molecular weight by fractionating the products to separate the desired boiling range and recycling higher boiling material.
The alkylnaphthalenes susceptible of recovery in the above-described hydrocarbon materials correspond to the following general formula:
where n is 1 to 8 and R is an alkyl radical containing generally from about 1 to 13 and preferably from about 1 to 5 carbon atoms. The total number of carbon atoms in alkyl groups attached to the naphthalene nucleus is generally from about 1 to'13 and preferably from about 1 to 5.
The present invention will be more clearly illustrated with the following example.
1HSTM-D878 Samples of the feedstock analyzed in (A) above, were hydrothermally treated in runs 1 to 5 using a thermal reactor. The conditions as well 'as the results for each of these runs are presented below in Table I.
3 Table 1 Run No Feed 1 2 3 4 5 Conditions:
Temperature, F Contact Time, Sec Hydrocarbon Partial Pressure, p.s.i.a. Hydrogen Partial Pressure, p.s.i.a. Concentration of Naphthalenes in Fractions, Wt. percent of Fraction:
450-475 F. Fraction (Naphthalene and Methylnaphthalone 475520 F. Fraction (Alkylnaphthanes, .W. 15 520560 F. Fraction (Alkylnaphthalenes, M.W. 17 EGO-600 )3. Fraction (Alkylnaphthalenes,
18 Total Alkylnaphthaleues,
Wt. percent Feed Naphthalene Yield, Wt.
percent Feed Alkylnaphthalenes Becovered, Wt. percent of Alkylnaphthalenes in Feed X Values lltisclaimed: r r. 1. A process for the recovery of alkylnaphthalenes trom petroleum hydrocarbon materials boiling in the temonds; said thermal conditions being employed in a relationship according 'to the following formula X tP where t is the contact time in seconds, P is the partial pressure of hydrogen in psi, P I is the partial pressure of hydrocarbon feed in p.s.i., e is the base of natural logarithms, R is the temperature in degrees Rankine, and X is between about ;1 and 100.
2. The process of claim 1 wherein X is between about 2 and 50.
3. A process for the recovery of alkylnaphthalenes from petroleum hydrocarbon materials boiling in the temperature range from about 300 to 800 F., said hydrocarbon materials including aromatics, olefins and about 20 to 80 weight percent of alkylnaphthalenes, the step comprising treating said hydrocarbon materials in the presence of hydrogen, in the absence of a catalyst and under thermal conditions including a temperature from about 1100 to 1350 F., a hydrocarbon partial pressure from about to 200 p.s.i.a., a hydrogen partial pressure from about 200 to 1000p.-s.i.a., and a contact time from about 0.5 to 200 seconds; said thermal conditions being employed in a relationship according to the following formula:
. 33.4 P l: ig -zeoon where t is the contact time in seconds, P isthe partial v and X is between about 1 and 100.
4. The process of claim 3 wherein X is between about 2 and 50.
References Cited in the file of this patent UNITED STATES PATENTS 2,754,340 Anderson et a1 June 10, 1956 2,858,348 Bosmaji'an et a1. Oct. 28, 1958' 2,920,116 Riesz et al. Jan. 5, 1960

Claims (1)

1. A PROCESS FOR THE RECOVERY OF ALKYLNAPHTHALENES FROM PETROLEUM HYDROCARBON MATERIALS BOILING IN THE TEMPERATURE RANGE FROM ABOUT 300 TO 800* F., SAID HYDROCARBON MATERIALS INCLUDING ABOUT 20 TO 80 WEIGHT PERCENT OF ALKYLNAPHTHALENES, THE STEP COMPRISING TREATING SAID HYDROCARBON MATERIALS IN THE PRESENCE OF HYDROGEN, IN THE ABSENCE OF A CATALYST AND UNDER THERMAL CONDITIONS INCLUDING A TEMPERATURE FROM ABOUT 1100* TO 1350* F., A HYDROCARBON PARTIAL PRESSURE FROM ABOUT 20 TO 200 P.S.I.A., A HYDROGEN PARTIAL PRESSURE FROM ABOUT 200 TO 1000 P.S.I.A., AND A CONTACT TIME FROM ABOUT 0.5 TO 200 SECONDS; SAID THERMAL CONDITIONS BEING EMPLOYED IN A RELATIONSHIP ACCORDING TO THE FOLLOWING FORMULA
US750082A 1958-07-22 1958-07-22 Non-catalytic process for the recovery of alkylnaphthalenes in the presence of hydrogen Expired - Lifetime US3083244A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298457A (en) * 1978-09-11 1981-11-03 University Of Utah Hydropyrolysis process for upgrading heavy oils and solids into light liquid products

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2754340A (en) * 1953-12-11 1956-07-10 Exxon Research Engineering Co Aromatics and resins production
US2858348A (en) * 1957-03-12 1958-10-28 Sinclair Refining Co Process for making naphthalene
US2920116A (en) * 1957-08-16 1960-01-05 United States Steel Corp Method of making naphthalene and lower-boiling compounds from creosote oil

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2754340A (en) * 1953-12-11 1956-07-10 Exxon Research Engineering Co Aromatics and resins production
US2858348A (en) * 1957-03-12 1958-10-28 Sinclair Refining Co Process for making naphthalene
US2920116A (en) * 1957-08-16 1960-01-05 United States Steel Corp Method of making naphthalene and lower-boiling compounds from creosote oil

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298457A (en) * 1978-09-11 1981-11-03 University Of Utah Hydropyrolysis process for upgrading heavy oils and solids into light liquid products
EP0068051A1 (en) * 1980-03-17 1983-01-05 The University Of Utah Hydropyrolysis process for converting heavy oils and solids into light liquid products

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