CN112552977A - Method for preparing synthetic ester base oil through step-by-step reaction - Google Patents
Method for preparing synthetic ester base oil through step-by-step reaction Download PDFInfo
- Publication number
- CN112552977A CN112552977A CN202011609500.7A CN202011609500A CN112552977A CN 112552977 A CN112552977 A CN 112552977A CN 202011609500 A CN202011609500 A CN 202011609500A CN 112552977 A CN112552977 A CN 112552977A
- Authority
- CN
- China
- Prior art keywords
- acid
- esterification reaction
- esterification
- reaction
- base oil
- 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.)
- Pending
Links
- 238000006243 chemical reaction Methods 0.000 title claims abstract description 63
- 150000002148 esters Chemical class 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 title claims abstract description 46
- 239000002199 base oil Substances 0.000 title claims abstract description 44
- 238000005886 esterification reaction Methods 0.000 claims abstract description 126
- 239000002253 acid Substances 0.000 claims abstract description 48
- 238000007670 refining Methods 0.000 claims abstract description 27
- 229920005862 polyol Polymers 0.000 claims abstract description 21
- 239000003054 catalyst Substances 0.000 claims abstract description 19
- 239000000203 mixture Substances 0.000 claims abstract description 13
- -1 polyol ester Chemical class 0.000 claims abstract description 12
- 150000003077 polyols Chemical class 0.000 claims abstract description 12
- 238000002156 mixing Methods 0.000 claims abstract description 10
- 239000000194 fatty acid Substances 0.000 claims description 17
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 17
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 15
- 229930195729 fatty acid Natural products 0.000 claims description 15
- 150000004665 fatty acids Chemical class 0.000 claims description 13
- 239000002994 raw material Substances 0.000 claims description 12
- 150000005846 sugar alcohols Polymers 0.000 claims description 10
- 239000003463 adsorbent Substances 0.000 claims description 9
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 9
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 3
- 229920000180 alkyd Polymers 0.000 claims description 2
- 239000011261 inert gas Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000003930 superacid Substances 0.000 claims description 2
- 230000032050 esterification Effects 0.000 abstract description 33
- 230000003197 catalytic effect Effects 0.000 abstract description 9
- 238000001914 filtration Methods 0.000 abstract description 8
- 230000002194 synthesizing effect Effects 0.000 abstract description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 5
- 239000010687 lubricating oil Substances 0.000 abstract description 4
- 239000010721 machine oil Substances 0.000 abstract description 4
- 238000003541 multi-stage reaction Methods 0.000 abstract description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 22
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 19
- 238000010438 heat treatment Methods 0.000 description 15
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 12
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 12
- 238000001816 cooling Methods 0.000 description 11
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 description 7
- 238000007872 degassing Methods 0.000 description 7
- XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 239000002131 composite material Substances 0.000 description 5
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 239000005643 Pelargonic acid Substances 0.000 description 3
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 239000003225 biodiesel Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 229940049964 oleate Drugs 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 238000001308 synthesis method Methods 0.000 description 2
- ARWLNYJOVMFZNY-KVVVOXFISA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;(z)-octadec-9-enoic acid Chemical compound OCC(CO)(CO)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O ARWLNYJOVMFZNY-KVVVOXFISA-N 0.000 description 1
- FMNZBNCPTJEVDS-KVVVOXFISA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;(z)-octadec-9-enoic acid Chemical compound CCC(CO)(CO)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O FMNZBNCPTJEVDS-KVVVOXFISA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- IGWVTTFOFTUUGY-UHFFFAOYSA-N CCCCCC(O)=O.CC(C)CCCC(O)=O Chemical compound CCCCCC(O)=O.CC(C)CCCC(O)=O IGWVTTFOFTUUGY-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- SKCMCXVYSJRFPA-UHFFFAOYSA-N heptanoic acid;nonanoic acid Chemical compound CCCCCCC(O)=O.CCCCCCCCC(O)=O SKCMCXVYSJRFPA-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- LPEKGGXMPWTOCB-GSVOUGTGSA-N methyl (R)-lactate Chemical compound COC(=O)[C@@H](C)O LPEKGGXMPWTOCB-GSVOUGTGSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/42—Complex esters, i.e. compounds containing at least three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compound: monohydroxy compounds, polyhydroxy compounds, monocarboxylic acids, polycarboxylic acids and hydroxy carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M177/00—Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/30—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
- C10M2207/301—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids used as base material
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
The invention relates to a method for preparing synthetic ester base oil by stepwise reaction, which comprises the steps of firstly synthesizing unsaturated polyol ester by esterification reaction of polyol and mixed monoacid under the condition of excessive alcohol, secondly, adding the unsaturated polyol ester into a reaction kettle containing the mixed monoacid in a dropwise manner to perform esterification reaction under the condition of excessive local acid, mixing a small amount of catalyst with the rest unsaturated ester at the later stage of the reaction, dropwise adding the mixture to perform catalytic esterification, refining and post-treating the mixture after the esterification is finished, filtering the mixture to obtain a refrigerating machine oil product with low acid value and good chromaticity, and simultaneously ensuring the product yield to be at a higher level, thereby having important significance for synthesizing high-quality synthetic ester lubricating oil base oil.
Description
Technical Field
The invention relates to a method for synthesizing high-purity refrigerating machine oil by reacting polyalcohol with mixed monoacid to obtain polyalcohol unsaturated ester, adding the polyalcohol unsaturated ester serving as a raw material into a reaction kettle containing the mixed monoacid in a dropwise manner, and carrying out esterification and refining post-treatment under the action of a catalyst.
The invention synthesizes the high-purity refrigerating machine oil through two-step esterification and refining post-treatment by controlling the molar ratio of the alcohol acid in the whole system. The first step is to esterify and synthesize unsaturated polyol ester with mixed monoacid under the condition of excessive alcohol, the second step is to take the unsaturated polyol ester as raw material and drop the raw material into a reaction kettle containing the mixed monoacid, a small amount of catalyst can be mixed and dropped with 10% unsaturated ester at the later stage of esterification, catalytic esterification is carried out under the condition of excessive local acid, the forward reaction is promoted, and the reaction rate is accelerated. After the esterification is finished, the high-quality synthetic ester base oil is obtained by refining and filtering.
Background
The polyol fatty acid ester refrigerator oil is one kind of high grade synthetic ester lubricating base oil. The lubricating oil can be used as special lubricating oil for refrigerating type compression devices and applied to lubrication, sealing and cooling of various refrigerators. The usual esterification processes to achieve high esterification levels and high reaction rates depend on extending the reaction time, raising the reaction temperature, increasing the acid excess ratio, using special catalysts, etc. But correspondingly increases the equipment loss, the impurity residue and the excessive acid cause the post-treatment refining process to be complex, and the three wastes are increased.
In the prior art, various polyol fatty acid ester preparation processes exist, for example, CN103710155A is a method for preparing biodiesel through high-temperature esterification of high-acid-value grease, high-acid-value grease and a catalyst are added into an esterification reactor, methanol is dripped into the esterification reactor by a dripping device for esterification, and a biodiesel product which is simple in process and easy to industrialize is obtained through post-distillation treatment. CN106187756A A D-methyl lactate esterification process, the process promotes the reaction to be carried out forward by adding methanol dropwise to bring water, the reaction temperature is low, and the purity of the finished product is high. CN109053441A A pentaerythritol oleic acid mixed ester with large bearing capacity and a synthetic method thereof, according to the following steps: pentaerythritol: the molar ratio of the succinic acid monoester is 3: 1: 1.1-1.2, synthesizing; CN108863785A A low pour point pentaerythritol oleate mixed ester and its synthesis method, adopting oleic acid, pentaerythritol, methyl maleate to synthesize; CN108707074A A method for preparing trimethylolpropane oleate with low acid value, which is synthesized by oleic acid, trimethylolpropane and micromolecular anhydride. The reaction processes all use catalysts and water-carrying agents, and simultaneously, the two-step synthesis method uses small molecular acid ester for carrying out hydroxyl end capping, and the procedures of washing and removing the water-carrying agents are added, so that the technical process is complex, and three wastes are increased. The method for synthesizing CN1381437 pentaerythritol oleate synthesizes the lubricant base oil with good high temperature resistance, good lubricating property, excellent viscosity-temperature property and good low-temperature fluidity by using excessive acid; CN108569964A A method for preparing neopentyl glycol ester, which adopts non-acid catalyst to esterify, and removes benzoic acid, isooctanoic acid and water-carrying agent at the later stage.
The above prior art processes rely on prolonged reaction time, increased reaction temperature, increased acid excess ratio, use of special catalysts, etc. to achieve high esterification and high reaction rates. But correspondingly increases the equipment loss, the impurity residue and the excessive acid cause the post-treatment refining process to be complex, and the three wastes are increased.
Disclosure of Invention
The invention aims to provide a method for preparing high-purity synthetic ester base oil through stepwise reaction, which synthesizes refrigerating machine oil through two steps of esterification and refining after controlling the same molar ratio of alcohol acid in the whole system.
In order to achieve the technical purpose, the invention adopts the following scheme:
a method for preparing synthetic ester base oil through step-by-step reaction is characterized by comprising the following steps:
(1) adding polyalcohol and mixed monobasic fatty acid into a first esterification reaction kettle to perform a first-step esterification reaction;
(2) adding the product of the first esterification reaction into a second esterification reaction kettle containing mixed monobasic fatty acid by adopting a dropwise adding method, and carrying out the second esterification reaction under the condition of excessive local acid;
(3) after the acid value of the reaction system is reduced to a specified range, mixing the product of the residual first-step esterification reaction with a catalyst, and continuously dropwise adding the mixture into the reaction system of the second-step esterification reaction to obtain crude synthetic ester base oil;
(4) and refining the crude synthetic ester base oil to obtain the finished synthetic ester base oil.
As a further improvement of the invention, the polyalcohol is one or more of neopentyl glycol, trimethylolpropane, pentaerythritol and dipentaerythritol.
As a further improvement of the invention, the mixed monobasic fatty acid is composed of two or more of monobasic fatty acids with carbon chain length of 4-9, including but not limited to butyric acid, valeric acid, caproic acid, enanthic acid, caprylic acid, pelargonic acid and isomeric acids thereof. Preferably, the raw materials in the first esterification reaction and the second esterification reaction are mixed with the same monobasic fatty acid component and the mixture ratio.
As a further improvement of the invention, the first esterification reaction and the second esterification reaction are carried out under the protection of inert gas.
As a further improvement of the method, in the first step of esterification reaction, the molar ratio of the polyol to the mixed monobasic fatty acid is 2: 1-3: 2.
As a further improvement of the method, the molar ratio of the raw material mixed monobasic fatty acid to the raw material polyol total alkyd related to the first esterification reaction and the second esterification reaction is 1: 1-1: 1.05.
As a further improvement of the method, the reaction temperature of the first esterification reaction is 160-240 ℃, and the preferable reaction temperature is 180-220 ℃.
As a further improvement of the method, the reaction temperature of the second esterification reaction is 150-200 ℃, and the preferable reaction temperature is 160-180 ℃.
As a further improvement of the invention, the catalyst is one or more of solid super acid, titanate and inorganic acid salt.
As a further improvement of the invention, the crude synthetic ester base oil is decolored by adopting an adsorbent, degassed under reduced pressure and filtered precisely to obtain the finished synthetic ester base oil.
As a further improvement of the invention, the adsorbent is one or more of activated clay, diatomite, alkaline bleaching earth, alumina and activated carbon.
As a further improvement of the invention, the adsorption temperature is 50-100 ℃;
as a further improvement of the invention, in the decompression degassing process, the temperature is 80-130 ℃, and the vacuum degree is-0.090-0.100 MPa.
The method comprises the steps of reacting step by step, synthesizing unsaturated polyol ester by esterification reaction of polyol and mixed monoacid under the condition of excessive alcohol, and adding the unsaturated polyol ester into a reaction kettle containing the mixed monoacid in a dropwise manner to perform esterification reaction under the condition of excessive local acid, so that the consumption of a catalyst can be reduced and excessive fatty acid can be reduced on the premise of ensuring the performance index of the product; in the later stage of the reaction, a small amount of catalyst can be used for mixing with the rest unsaturated ester and then dropwise adding the mixture for catalytic esterification, so that the reaction is promoted to be carried out in the forward direction, and the reaction rate is increased. After esterification, the product is refined and then filtered to obtain the refrigerator oil product with low acid value and good chromaticity, and meanwhile, the product yield is at a higher level, so that the method has important significance for synthesizing high-quality synthetic ester lubricating oil base oil.
Drawings
FIG. 1 is a process flow diagram of the process of the present invention.
FIG. 2 is a schematic diagram of the esterification process of the experimental apparatus of the present invention, in which:
1-first esterification reaction kettle (first stage esterification), 2-condensing equipment I, 3-second esterification reaction kettle (catalytic esterification), 4-refining reaction kettle, 5-1-pump I, 5-2-pump II, 5-3-pump III, 5-4-pump IV, 6-finished product receiving device, 7-condensing equipment II, 8-esterified water receiving device.
Detailed Description
In order to better illustrate the invention, we will cite the following examples, but the invention is not limited to the following examples.
The apparatus used in the example is shown in fig. 2, a first esterification reaction vessel 1, a second esterification reaction vessel 3, a refining reaction vessel 4, and a finished product receiving apparatus 6 are connected in sequence according to the procedure, and a pump i 5-1, a pump ii 5-2, and a pump iii 5-3 are used as material pumps to pump the product into the next reaction vessel/finished product receiving apparatus. The first esterification reaction kettle 1 and the second esterification reaction kettle 3 are respectively connected with a condensing device I2 and a condensing device II 7, mixed steam of fatty acid and water escaping from the reaction is cooled and split, an oil phase returns to the first esterification reaction kettle 1 and the second esterification reaction kettle 3 respectively to continue to participate in the reaction, and a water phase is sent to an esterification water receiving device 8 through a pump IV 5-4.
And (3) carrying out a first-step esterification reaction in the first esterification reaction kettle 1, delivering the product after the reaction to a liquid dropping device at a feed inlet of the second esterification reaction kettle 3 through a pump I5-1, and introducing the product into the second esterification reaction kettle 3 in a dropping mode to carry out a second-step esterification reaction. Initially carrying out esterification reaction under the condition of excessive local acid, uniformly mixing the residual esterification product in the first esterification reaction kettle 1 and a small amount of catalyst after the central control acid value is less than a specified range, and then dropwise adding the mixture into the second esterification reaction kettle 3 to prepare the crude synthetic ester base oil.
The crude synthetic ester base oil is sent into a refining reaction kettle 4 through a pump II 5-2, an adsorbent is added for adsorption, then vacuum pressure reduction degassing and precise filtration are carried out, and a product is sent into a finished product receiving device 6 through a pump III 5-3.
Example 1
Referring to fig. 1, the process flow for preparing the synthetic ester base oil i by using pentaerythritol, isooctanoic acid and isononanoic acid as raw materials is as follows:
carrying out esterification reaction of pentaerythritol, isooctanoic acid and isononanoic acid in a first esterification reaction kettle 1, adding 13.6kg of pentaerythritol, 14.4kg of isooctanoic acid and 15.8kg of isononanoic acid into the esterification reaction kettle, slowly heating to 220-230 ℃ under the protection of nitrogen, stirring for reaction until the acid value of the system is less than 0.01mgKOH/g, and cooling to obtain polyhydric alcohol unsaturated ester I;
carrying out esterification reaction of polyol unsaturated ester I, isooctanoic acid and isononanoic acid in a second esterification reaction kettle 3, adding 14.4kg of isooctanoic acid and 15.8kg of isononanoic acid into the reaction kettle, slowly raising the temperature to 180 ℃ under the protection of nitrogen, adding the esterification product in a first esterification reaction kettle 1 in a dropwise manner, carrying out esterification reaction under the condition of excessive local acid, controlling the acid value to be less than 16mgKOH/g, uniformly mixing the rest esterification product in the first esterification reaction kettle 1 and a small amount of catalyst (0.5 thousandth titanate) and continuously adding the mixture into the reaction kettle in a dropwise manner to carry out catalytic esterification reaction until the acid value of the system is less than 0.01mgKOH/g, and cooling to obtain crude synthetic ester base oil I;
refining the crude synthetic ester base oil I in a refining reaction kettle 4, adding a specified amount of composite adsorbent into the reaction kettle, heating to 70-80 ℃, refining and adsorbing for 2 hours, slowly heating to 100 ℃, degassing for 1 hour under the vacuum degree of-0.090-0.100 Mpa, and precisely filtering to obtain the synthetic ester base oil I.
The acid value of the pentaerythritol isooctanoate isononanoate product is 0.01mgKOH/g, the hydroxyl value is 4.7 mgKOH/g, and the yield is 85.55%. The viscosity of the obtained product at 40 deg.C is 50-300mm2/s。
Example 2
Referring to fig. 1, the process flow for preparing the synthetic ester base oil ii by using neopentyl glycol, n-pentanoic acid and nonanoic acid as raw materials is as follows:
carrying out esterification reaction of neopentyl glycol, n-pentanoic acid and nonanoic acid in a first esterification reaction kettle 1, adding 28.45kg of neopentyl glycol, 15kg of n-pentanoic acid and 20kg of nonanoic acid into the esterification reaction kettle, slowly heating to 210 ℃ and 220 ℃ under the protection of nitrogen, stirring for reaction until the acid value of the system is less than 0.01mgKOH/g, and cooling to obtain polyol unsaturated ester II;
carrying out esterification reaction of polyol unsaturated ester II, n-valeric acid and pelargonic acid in a second esterification reaction kettle 3, adding 15kg of n-valeric acid and 20kg of pelargonic acid into the reaction kettle, slowly raising the temperature to 170 ℃ under the protection of nitrogen, adding the esterification product in the first esterification reaction kettle 1 in a dropwise manner, carrying out esterification reaction under the condition of excessive local acid, controlling the acid value to be less than 18mgKOH/g, uniformly mixing the rest esterification product in the first esterification reaction kettle 1 with a small amount of catalyst (0.5 thousandth of super-strong solid acid), continuously adding the mixture into the reaction kettle in a dropwise manner to carry out catalytic esterification reaction until the acid value of the system is less than 0.05mgKOH/g, and cooling to obtain crude synthetic ester base oil II;
refining the crude synthetic ester base oil II in a refining reaction kettle 4, adding a specified amount of composite adsorbent into the reaction kettle, heating to 60-70 ℃, refining and adsorbing for 1.5-2 hours, slowly heating to 90 ℃, degassing under the vacuum degree of-0.090-0.100 Mpa for 1 hour under reduced pressure, and precisely filtering to obtain the synthetic ester base oil II.
The neopentyl glycol n-pentanoic pelargonic acid ester product has an acid value of 0.05mgKOH/g, a hydroxyl value of 5.7 mgKOH/g and a yield of 87.55%. The viscosity of the obtained product at 40 deg.C is 40-300mm2/s。
Example 3
Referring to fig. 1, the process flow for preparing the synthetic ester base oil iii by taking pentaerythritol, heptanoic acid and hexanoic acid as raw materials is as follows:
carrying out esterification reaction of pentaerythritol, heptanoic acid and hexanoic acid in a first esterification reaction kettle 1, adding 14.05kg of pentaerythritol, 10kg of heptanoic acid and 13.6kg of hexanoic acid into the esterification reaction kettle, slowly heating to 220-230 ℃ under the protection of nitrogen, stirring for reaction until the acid value of the system is less than 0.01mgKOH/g, and cooling to obtain polyhydric alcohol unsaturated ester III;
carrying out esterification reaction of polyol unsaturated ester III, heptanoic acid and n-hexanoic acid in a second esterification reaction kettle 3, adding 10kg of heptanoic acid and 13.6kg of n-hexanoic acid into the reaction kettle, slowly raising the temperature to 190 ℃ under the protection of nitrogen, adding an esterification product in a first esterification reaction kettle 1 in a dropwise manner, carrying out esterification reaction under the condition of excessive local acid, controlling the acid value to be less than 17mgKOH/g, uniformly mixing the esterification product in the rest first esterification reaction kettle 1 and a small amount of catalyst (0.5 per thousand titanate), continuously adding the mixture into the reaction kettle in a dropwise manner to carry out catalytic esterification reaction until the acid value of the system is less than 0.1mgKOH/g, and cooling to obtain crude synthetic ester base oil III;
refining the crude synthetic ester base oil III in a refining reaction kettle 4, adding a specified amount of composite adsorbent into the reaction kettle, heating to 70-80 ℃, refining and adsorbing for 2 hours, slowly heating to 100 ℃, degassing under the vacuum degree of-0.090-0.100 Mpa for 1 hour under reduced pressure, and precisely filtering to obtain the synthetic ester base oil III.
The acid value of the pentaerythritol isoheptanoic acid n-hexanoate product is 0.1mgKOH/g, the hydroxyl value is 3.7 mgKOH/g, and the yield is 86.75%. The viscosity of the obtained product at 40 deg.C is 50-300mm2/s。
Example 4
Referring to fig. 1, the process flow for preparing the synthetic ester base oil iv by using dipentaerythritol, heptanoic acid and nonanoic acid as raw materials is as follows:
carrying out esterification reaction of pentaerythritol, heptanoic acid and nonanoic acid in a first esterification reaction kettle 1, adding 25.4kg of dipentaerythritol, 23.4kg of heptanoic acid and 34.8kg of nonanoic acid into the esterification reaction kettle, slowly heating to 180-190 ℃ under the protection of nitrogen, stirring for reaction until the acid value of the system is less than 0.01mgKOH/g, and cooling to obtain polyhydric alcohol unsaturated ester IV;
carrying out esterification reaction of polyol unsaturated ester IV, heptanoic acid and nonanoic acid in a second esterification reaction kettle 3, adding 15.6kg of heptanoic acid and 17.4kg of nonanoic acid into the reaction kettle, slowly raising the temperature to 160 ℃ under the protection of nitrogen, adding the esterification product in the first esterification reaction kettle 1 in a dropwise manner, carrying out esterification reaction under the condition of excessive local acid, controlling the acid value to be less than 14mgKOH/g, uniformly mixing the rest esterification product in the first esterification reaction kettle 1 and a small amount of catalyst (0.5 per thousand titanate), continuously adding the mixture into the reaction kettle in a dropwise manner to carry out catalytic esterification reaction until the acid value of the system is less than 0.1mgKOH/g, and cooling to obtain crude synthetic ester base oil IV;
refining the crude synthetic ester base oil IV in a refining reaction kettle 4, adding a specified amount of composite adsorbent into the reaction kettle, heating to 70-80 ℃, refining and adsorbing for 2 hours, slowly heating to 100 ℃, degassing for 1 hour under the vacuum degree of-0.090-0.100 Mpa, and performing precise filtration to obtain the synthetic ester base oil IV.
The dipentaerythritol heptanoic acid pelargonic acid ester product has an acid value of 0.1mgKOH/g, a hydroxyl value of 2.5mgKOH/g and a yield of 88.59%. The obtained product has viscosity of 80-350mm at 40 deg.C2/s。
Example 5
Referring to fig. 1, the process flow for preparing the synthetic ester base oil v from pentaerythritol, neopentyl glycol, butyric acid and n-hexanoic acid as raw materials is as follows:
carrying out esterification reaction of pentaerythritol, neopentyl glycol, butyric acid and n-hexanoic acid in a first esterification reaction kettle 1, adding 13.6kg of dipentaerythritol, 10.4kg of neopentyl glycol, 13.2kg of butyric acid and 17.4kg of n-hexanoic acid into the esterification reaction kettle, slowly heating to 190-210 ℃ under the protection of nitrogen, stirring for reaction until the acid value of a system is less than 0.01mgKOH/g, and cooling to obtain polyhydric alcohol unsaturated ester V;
carrying out esterification reaction of unsaturated polyol ester V, butyric acid and n-hexanoic acid in a second esterification reaction kettle 3, adding 13.2kg of butyric acid and 17.4kg of n-hexanoic acid into the reaction kettle, slowly raising the temperature to 200 ℃ under the protection of nitrogen, adding an esterification product in a first esterification reaction kettle 1 in a dropwise manner, carrying out esterification reaction under the condition of excessive local acid, controlling the acid value to be less than 19mgKOH/g, uniformly mixing the esterification product in the rest first esterification reaction kettle 1 and a small amount of catalyst (0.5 per thousand titanate), continuously adding the mixture into the reaction kettle in a dropwise manner to carry out catalytic esterification reaction until the acid value of the system is less than 0.1mgKOH/g, and cooling to obtain crude synthetic ester base oil V;
refining the crude synthetic ester base oil V in a refining reaction kettle 4, adding a specified amount of composite adsorbent into the reaction kettle, heating to 70-80 ℃, refining and adsorbing for 2 hours, slowly heating to 100 ℃, degassing for 1 hour under the vacuum degree of-0.090-0.100 Mpa, and precisely filtering to obtain the synthetic ester base oil V.
The acid value of the synthesized ester base oil V product is 0.1mgKOH/g, the hydroxyl value is 6.1mgKOH/g, and the yield is 86.23%. The obtained product has viscosity of 20-60mm at 40 deg.C2/s。
Claims (10)
1. A method for preparing synthetic ester base oil through step-by-step reaction is characterized by comprising the following steps:
(1) adding polyalcohol and mixed monobasic fatty acid into a first esterification reaction kettle to perform a first-step esterification reaction;
(2) adding the product of the first esterification reaction into a second esterification reaction kettle containing mixed monobasic fatty acid by adopting a dropwise adding method, and carrying out the second esterification reaction under the condition of excessive local acid;
(3) after the acid value of the reaction system is reduced to a specified range, mixing the product of the residual first-step esterification reaction with a catalyst, and continuously dropwise adding the mixture into the reaction system of the second-step esterification reaction to obtain crude synthetic ester base oil;
(4) and refining the crude synthetic ester base oil to obtain the finished synthetic ester base oil.
2. The method according to claim 1, wherein the mixed mono-fatty acid is composed of two or more of mono-fatty acids having a carbon chain length of 4 to 9.
3. The method of claim 1, wherein the polyol is one or more of neopentyl glycol, trimethylolpropane, pentaerythritol, dipentaerythritol.
4. The method of claim 1, wherein the first and second esterification reactions are carried out under an inert gas blanket.
5. The method according to claim 1, wherein in the first esterification reaction, the molar ratio of the polyol to the mixed monobasic fatty acid is 2: 1-3: 2.
6. The method according to claim 1, wherein the molar ratio of the raw material polyol to the mixed monobasic fatty acid total alkyd is 1: 1-1: 1.05 in the first and second esterification reactions.
7. The method according to claim 1, wherein the reaction temperature of the first esterification reaction is 160 to 240 ℃, preferably 180 to 220 ℃.
8. The process according to claim 1, wherein the reaction temperature of the second esterification reaction is 150 to 200 ℃, preferably 160 to 180 ℃.
9. The method of claim 1, wherein the catalyst is one or more of a solid super acid, a titanate, and an inorganic acid salt.
10. The method of claim 1, wherein the crude synthetic ester base oil is decolorized with an adsorbent, degassed under reduced pressure, and precision filtered to obtain a finished synthetic ester base oil.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011609500.7A CN112552977A (en) | 2020-12-30 | 2020-12-30 | Method for preparing synthetic ester base oil through step-by-step reaction |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011609500.7A CN112552977A (en) | 2020-12-30 | 2020-12-30 | Method for preparing synthetic ester base oil through step-by-step reaction |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN112552977A true CN112552977A (en) | 2021-03-26 |
Family
ID=75034501
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202011609500.7A Pending CN112552977A (en) | 2020-12-30 | 2020-12-30 | Method for preparing synthetic ester base oil through step-by-step reaction |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN112552977A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113173849A (en) * | 2021-04-25 | 2021-07-27 | 中国石油化工股份有限公司 | Pentaerythritol ester base oil and preparation method thereof |
| CN113861024A (en) * | 2021-10-08 | 2021-12-31 | 上海多纶化工有限公司 | Preparation method of fatty acid polyglycol ester |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3670013A (en) * | 1969-10-16 | 1972-06-13 | Hercules Inc | Synthesis of partial esters of certain poly(neopentyl polyols) and aliphatic monocarboxylic acids |
| US5895778A (en) * | 1997-08-25 | 1999-04-20 | Hatco Corporation | Poly(neopentyl polyol) ester based coolants and improved additive package |
| US20020193260A1 (en) * | 2001-01-05 | 2002-12-19 | Mchenry Michael A. | Biodegradable polyneopentyl polyol based synthetic ester blends and lubricants thereof |
| CN102272273A (en) * | 2009-01-16 | 2011-12-07 | 科聚亚公司 | Carbon dioxide-based working fluids for refrigeration and air conditioning systems |
| CN102292420A (en) * | 2009-01-26 | 2011-12-21 | 科聚亚公司 | Production of polyol ester lubricants for refrigeration systems |
| CN102304410A (en) * | 2005-07-27 | 2012-01-04 | 卢布里佐尔公司 | High viscosity synthetic ester lubricant base stock blends |
| CN104093822A (en) * | 2013-02-05 | 2014-10-08 | 科聚亚公司 | Refrigeration oil and compositions with hydrocarbon refrigerants |
| US20150018260A1 (en) * | 2012-02-28 | 2015-01-15 | Petroliam Nasional Berhad | Lubricant composition of matter and methods of preparation |
-
2020
- 2020-12-30 CN CN202011609500.7A patent/CN112552977A/en active Pending
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3670013A (en) * | 1969-10-16 | 1972-06-13 | Hercules Inc | Synthesis of partial esters of certain poly(neopentyl polyols) and aliphatic monocarboxylic acids |
| US5895778A (en) * | 1997-08-25 | 1999-04-20 | Hatco Corporation | Poly(neopentyl polyol) ester based coolants and improved additive package |
| US20020193260A1 (en) * | 2001-01-05 | 2002-12-19 | Mchenry Michael A. | Biodegradable polyneopentyl polyol based synthetic ester blends and lubricants thereof |
| CN102304410A (en) * | 2005-07-27 | 2012-01-04 | 卢布里佐尔公司 | High viscosity synthetic ester lubricant base stock blends |
| CN102272273A (en) * | 2009-01-16 | 2011-12-07 | 科聚亚公司 | Carbon dioxide-based working fluids for refrigeration and air conditioning systems |
| CN102292420A (en) * | 2009-01-26 | 2011-12-21 | 科聚亚公司 | Production of polyol ester lubricants for refrigeration systems |
| CN103695129A (en) * | 2009-01-26 | 2014-04-02 | 科聚亚公司 | Working fluid comprising polyol ester lubricant |
| US20150018260A1 (en) * | 2012-02-28 | 2015-01-15 | Petroliam Nasional Berhad | Lubricant composition of matter and methods of preparation |
| CN104093822A (en) * | 2013-02-05 | 2014-10-08 | 科聚亚公司 | Refrigeration oil and compositions with hydrocarbon refrigerants |
Non-Patent Citations (3)
| Title |
|---|
| 王亚楼: "《化学制药工艺学》", 31 October 2008, 化学工业出版社 * |
| 许苗军: "《有机化学实验》", 31 August 2017, 中国农业大学出版社 * |
| 马鸿飞: "《有机化学及单元反应》", 30 November 1997, 中国矿业大学出版社 * |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113173849A (en) * | 2021-04-25 | 2021-07-27 | 中国石油化工股份有限公司 | Pentaerythritol ester base oil and preparation method thereof |
| CN113173849B (en) * | 2021-04-25 | 2023-03-07 | 中国石油化工股份有限公司 | Pentaerythritol ester base oil and preparation method thereof |
| CN113861024A (en) * | 2021-10-08 | 2021-12-31 | 上海多纶化工有限公司 | Preparation method of fatty acid polyglycol ester |
| CN113861024B (en) * | 2021-10-08 | 2024-03-15 | 上海多纶化工有限公司 | Preparation method of fatty acid polyethylene glycol ester |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN112552977A (en) | Method for preparing synthetic ester base oil through step-by-step reaction | |
| CN102796603B (en) | Method for preparing lithium lubricating grease | |
| CA2366414C (en) | Method and apparatus for preparing fatty acid esters | |
| CN112552976A (en) | Complex ester type refrigerator oil and synthetic method thereof | |
| CN106750244B (en) | A method of polyether polyol is prepared using micro passage reaction | |
| WO2011106186A1 (en) | Estolide derivatives useful as biolubricants | |
| CN109576063B (en) | Method for synthesizing low-sulfur diesel antiwear agent by one-step method | |
| EP2694630A1 (en) | Estolide derivatives useful as biolubricants | |
| CN102260571B (en) | Novel aviation base oil | |
| CN101117587B (en) | Mobile biodiesel production facility and its process flow | |
| CN102585201A (en) | Method for preparing polyol for hard polyurethane foam by using kitchen waste | |
| CN110669583B (en) | Vegetable insulating oil refining process with rapeseed oil as raw material | |
| CN111363578B (en) | Method for refining mesophase pitch by hydrogenation and chain transfer modification | |
| CN218710201U (en) | System for preparing special oil for cold liquid from naphthenic base distillate oil | |
| CN114085190B (en) | Ionic liquid, composition and preparation method thereof | |
| CN111892950A (en) | Method for producing needle coke by combined process | |
| JP2003049192A (en) | Method for producing monoglyceride | |
| CN100460482C (en) | Method of preparing organism diesel oil from mixing plant oil | |
| CN111807927A (en) | Production device and preparation method of organic sodium alkoxide | |
| CN117384672A (en) | Preparation method of degradable bio-based base oil | |
| EP3924453A1 (en) | Novel traction fluid with improved low temperature properties | |
| CN111116775A (en) | Process and apparatus for preparing low viscosity poly α -olefins | |
| CN109678716B (en) | Continuous production process of oligomeric adipic acid diol ester | |
| CN115710528B (en) | Efficient refrigerator oil composition and preparation method thereof | |
| CN111073702B (en) | Hydrotreating system and method for high-viscosity poly-alpha-olefin synthetic oil |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20210326 |