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CN101875609A - Method for preparing PVC plasticizer from by-products of production of fumaric acid and recovery alcohol - Google Patents

Method for preparing PVC plasticizer from by-products of production of fumaric acid and recovery alcohol Download PDF

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Publication number
CN101875609A
CN101875609A CN2010101911668A CN201010191166A CN101875609A CN 101875609 A CN101875609 A CN 101875609A CN 2010101911668 A CN2010101911668 A CN 2010101911668A CN 201010191166 A CN201010191166 A CN 201010191166A CN 101875609 A CN101875609 A CN 101875609A
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alcohol
temperature
fumaric acid
recovery
production
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CN2010101911668A
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CN101875609B (en
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曹锋
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ZHENJIANG UNION CHEMICAL INDUSTRY Co Ltd
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ZHENJIANG UNION CHEMICAL INDUSTRY Co Ltd
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Abstract

The invention relates to a method for preparing a PVC plasticizer by taking by-products of production of fumaric acid and recovery alcohol as raw materials. The method comprises the following steps of: 1, adding 1 part of acid water residues, 2 to 4 parts of recovery isooctanol or recovery isononyl alcohol and 200 to 400ppm of esterification catalyst into a reactor with a thermometer, a distillation and condensing device and a stirring device, and heating the mixture with stirring to the temperature of between 120 and 160 DEG C for yielding water; 2, continuing heating to the highest reaction temperature of 220 DEG C, controlling the temperature of cut fraction to be between 80 and 102 DEG C all the time in the process of a reaction, and reacting until an acid value is less than 1.0 mgKOH/g; and 3, reducing the temperature until the temperature is 190 DEG C or 215 DEG C, performing dealcoholization under the reduced pressure of between -600 and -740 mmHg for 1 to 2 hours, stopping the reaction, and cooling and filtering to obtain a finished product. The method can utilize scrap materials of enterprises effectively, reduce the production cost of the plasticizer and the treatment cost of waste liquor and reduce environmental pollution.

Description

Produce by product and reclaim the method that alcohol prepares the PVC softening agent with fumaric acid
Technical field
The present invention relates to a kind of is the method for feedstock production PVC softening agent with fumaric acid production by product (sour water slag) with reclaiming alcohol (isooctyl alcohol or isononyl alcohol).
Background technology
There is research to use the reported in literature of fumaric acid and the synthetic softening agent diisooctyl fumarate of isooctyl alcohol at present.Research hydrogen sulfates such as the Liu Xue of department of chemistry of Huaibei Coal Normal College is gorgeous are received the synthetic of catalysis diisooctyl fumarate, are raw material with fumaric acid and isooctyl alcohol, and NaHSO4 makees catalyzer, and toluene is made the band aqua, has synthesized diisooctyl fumarate.Guangxi Normal University's chemical is that Liao Ping moral etc. has been studied method and the processing condition that anhydrous cupric sulfate is done catalyzer synthetic diisooctyl fumarate.Other softening agent synthetic document and patent reports such as research DEF, non-toxic plasticizer, low molecular weight polyester plasticiser are arranged in addition.It is a kind of new chemical mould inhibitor that 2004 3 phases " fine chemistry industry economy and technical intelligence " are introduced DEF (DEF), has low toxicity, efficient, use and be not subjected to pH value limitation, advantages such as noresidue, be commonly used for organic synthesis intermediate, internal plasticizer and solvent, the employing hydrogen sulfate receives and aluminum chloride is catalyzer, replaces the sulfuric acid and the hydrochloric acid of severe corrosive, with cis-butenedioic anhydride and ethanol is raw material, has synthesized DEF.The softening agent cost of these method preparations is higher.
Sour water slag production process: the tail gas that phthalic anhydride production produces forms sour water after washing, the sour water composition is mainly: MALEIC ANHYDRIDE, methyl-maleic acid, phenylformic acid, phthalic anhydride etc., sour water is produced fumaric acid through purifying, make with extra care, reacting, and remaining mixing acid sludge is the sour water slag.The main component of sour water slag is the mixing acid that acid such as fumaric acid, MALEIC ANHYDRIDE, methyl-maleic acid, phthalic anhydride, phenylformic acid are formed.Large-scale phthalic anhydride manufacturing enterprise has hundreds of tons spent acid grain slag to produce every year, handles these waste materials and will spend great amount of cost.How low-cost processes, these waste materials of recycle alleviate company's operation burden and become the problem that the assistant officer of each manufacturing enterprise need solve.
Reclaim alcohol: softening agent such as DOP, DINP need underpressure distillation that excessive alcohol is deviate from for reclaiming alcohol in the reaction later stage, and its main component is isooctyl alcohol or isononyl alcohol (more than 80%), remains to be monoesters and other ester class.
Summary of the invention
Technical problem to be solved by this invention is, providing a kind of can be the low-grade PVC softening agent of raw material production with above-mentioned waste, reduces producing by product and reclaim the method that alcohol prepares the PVC softening agent with fumaric acid of softening agent manufacturing cost and fumaric acid production offal treatment cost.
Method process following steps of the present invention:
The first step: adding sour water slag and molfraction are 2~4 parts recovery isooctyl alcohol or reclaim isononyl alcohol in the reactor that thermometer, distillation condensing works, whipping appts are housed, the molfraction that the add-on of sour water slag is converted to fumaric acid is 1 part, adds the esterifying catalyst of 200~400ppm, heat temperature raising to 120 under stirring state~160 ℃ water outlet again;
Second step: continuing to be warming up to maximum temperature is 220 ℃, and reaction process is controlled all the time and heated up in a steamer 80~102 ℃ of temperature, reacts to acid number to be<1.0mgKOH/g;
The 3rd step: cooling, when what use in the first step is to be cooled to 195 ℃ when reclaiming isooctyl alcohol, be cooled to 215 ℃ when what use in the first step when reclaiming isononyl alcohol ,-600~-dealcoholysis of reducing pressure under the 740mmHg condition was a stopped reaction in 1~2 hour, cooling is filtered and is got product.
The inventive method successfully utilizes plasticizer production enterprise at the pure Di File softening agent of Chenging with sour water slag He of the recovery of producing DOP, the generation of DINP process, the assessment result that its performance is done shows, the inventive method institute synthetic softening agent can be used as low-grade cheap softening agent and carries out volume production and use, has effectively utilized scrap materials of enterprises, has reduced production cost and treatment cost of waste liquor, has reduced environmental pollution.
Embodiment
The step of embodiments of the invention is as follows:
The first step: in the reactor that thermometer, distillation condensing works (chuck is arranged), whipping appts are housed, add 1 part of sour water slag, 3.0 parts of recovery isooctyl alcohol, the esterifying catalyst (tin oxalate compounds) that adds 250ppm again, heat temperature raising is to water outlet (120~160 ℃) under stirring state, second step: continuing to be warming up to maximum temperature is 220 ℃, reaction process is controlled all the time and is heated up in a steamer a temperature at 90~102 ℃, react to acid number less than 1.0mgKOH/g; The 4th step: be cooled to 195 ℃, (680mmHg) stopped reaction after 1 hour, cooling is filtered and is got product, and collects the alcohol of deviating from simultaneously and prepares against recycle in the dealcoholysis of reducing pressure.
It is as follows that the product of the embodiment of the invention detects index:
1. product chemical property:
Project Acid number mgKOH/g Moisture % Viscosity cps Alcohol content %
Data ??0.40 ??0.0736 ??30.6 ??0.1687
2. plasticizing efficiency and aging resistance:
2.1 plasticizing efficiency
The softening agent addition Hardness (Shore A.15sec)
?DOP ??60 ??79
Present embodiment was according to 1: 1 blending DOP ??60 ??80
2.2 machinery and aging resistance
Figure BSA00000153132800031
The test piece preparatory condition
Take out the sheet temperature: 165 ℃, take out the sheet time: 5min compressing tablet temperature: 170 ℃, the compressing tablet time: 8min
Aging condition: 100 ℃ of * 168hr
Measuring mechanical property temperature: 25 ℃
Used plant and instrument: two running roller machines (the deep sun in Shanghai), tabletting machine (inscription Yu electronics technology company limited), ageing oven (inscription Yu electronics technology company limited), puller system (High Speed Rail Testing Instruments company limited), Shore durometer (Wuxi Qian Zhou surveying instrument factory)
Test piece prescription: PVC powder (S-65) 100g, softening agent 60g, stablizer 3g
Brief summary:
This product and DOP according to blending in 1: 1 after its plasticizing efficiency approaching substantially with DOP, machinery and aging resistance are also more approaching with DOP, but color is dark than DOP, can be used for color depth and reaches in the less demanding PVC goods of color.

Claims (1)

1. produce by product and reclaim the method method that alcohol prepare the PVC softening agent with fumaric acid for one kind, it is characterized in that: the process following steps,
The first step: adding sour water slag and molfraction are 2~4 parts recovery isooctyl alcohol or reclaim isononyl alcohol in the reactor that thermometer, distillation condensing works, whipping appts are housed, the molfraction that the add-on of sour water slag is converted to fumaric acid is 1 part, adds the esterifying catalyst of 200~400ppm, heat temperature raising to 120 under stirring state~160 ℃ water outlet again;
Second step: continuing to be warming up to maximum temperature is 220 ℃, and reaction process is controlled all the time and heated up in a steamer 80~102 ℃ of temperature, reacts to acid number to be<1.0mgKOH/g;
The 3rd step: cooling, when what use in the first step is to be cooled to 195 ℃ when reclaiming isooctyl alcohol, be cooled to 215 ℃ when what use in the first step when reclaiming isononyl alcohol ,-600~-dealcoholysis of reducing pressure under the 740mmHg condition was a stopped reaction in 1~2 hour, cooling is filtered and is got product.
CN 201010191166 2010-06-04 2010-06-04 Method for preparing PVC plasticizer from by-products of production of fumaric acid and recovery alcohol Active CN101875609B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201010191166 CN101875609B (en) 2010-06-04 2010-06-04 Method for preparing PVC plasticizer from by-products of production of fumaric acid and recovery alcohol

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Application Number Priority Date Filing Date Title
CN 201010191166 CN101875609B (en) 2010-06-04 2010-06-04 Method for preparing PVC plasticizer from by-products of production of fumaric acid and recovery alcohol

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CN101875609B CN101875609B (en) 2013-04-10

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1257472A (en) * 1997-05-22 2000-06-21 塞拉尼斯有限公司 Method for producing ester plasticizers
US20020028963A1 (en) * 2000-09-05 2002-03-07 Oxeno Olefinchemie Gmbh Process for preparing carboxylic esters
CN101298506A (en) * 2008-06-05 2008-11-05 中山联成化学工业有限公司 PVC plasticizer synthesized by phthalic anhydride by-product and corn mixed alcohol

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1257472A (en) * 1997-05-22 2000-06-21 塞拉尼斯有限公司 Method for producing ester plasticizers
US20020028963A1 (en) * 2000-09-05 2002-03-07 Oxeno Olefinchemie Gmbh Process for preparing carboxylic esters
CN101298506A (en) * 2008-06-05 2008-11-05 中山联成化学工业有限公司 PVC plasticizer synthesized by phthalic anhydride by-product and corn mixed alcohol

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
王箴: "《化工辞典》", 31 August 2000, 化学工业出版社 *

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