CN1431240A - Method for preparing polyether ester polyalcohol - Google Patents
Method for preparing polyether ester polyalcohol Download PDFInfo
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- CN1431240A CN1431240A CN 01130466 CN01130466A CN1431240A CN 1431240 A CN1431240 A CN 1431240A CN 01130466 CN01130466 CN 01130466 CN 01130466 A CN01130466 A CN 01130466A CN 1431240 A CN1431240 A CN 1431240A
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- preparation
- epoxide
- small molecules
- acid anhydride
- polyester ether
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Abstract
A process for preparing polyether polyol includes such steps as proportionally adding micromolecular polyether, cyclic acid anhydride and catalyst to high-pressure reactor, vacuumizing, filling N2, heating to 50-200 deg.c, adding epoxy compound and polymerizing. Its advantage is high transform rate.
Description
Technical field:
The invention belongs to a kind of preparation method of polyester ether polylol, relate in particular to a kind of preparation method who is used to produce the polyester ether polylol of urethane.
Background technology:
Polyurethane material is a kind of novel superpolymer with special performance and many-sided purposes, is widely used in the industry such as urethane foam, rubber, coating, tackiness agent, synthon, synthetic leather, water-proof grouting agent with its excellent performance.Urethane is that the basic raw material addition polymerization forms with vulcabond and polyvalent alcohol, wherein polyol compound comprises polyester type and polyether-type two big classes, the intensity of PAUR goods, wear-resisting, tear-resistant, oil-proofness is better, but its hydrolytic resistance and lower temperature resistance are comparatively inferior, and procedure of processing is also more.And the hydrolysis of polyether(poly)urethane, anti-mould, anti-deflection, resistance to low temperature are good, and process operation is convenient, but thermotolerance and wear resistance are not good enough.People wish always and can overcome the two shortcoming improving every physicals that its mechanical property and stable on heating while still can keep polyether(poly)urethane and lower cost for many years, respectively get the chief.Therefore, the someone proposes to prepare urethane with esterification polyether glycol or polyethers, polyester mixed type polyvalent alcohol.Poland Gdansk scholar Poominka-Micaalak of university, Lisowska R and Balas A. etc. carry out synthetic polyurethane elastomer after the physical mixed to polyethers, two kinds of polyvalent alcohols of polyester, have better comprehensive performance.But the high viscosity of polyester composition is often made troubles to operation during physical mixed, and the consistency of polyester and polyethers is relatively poor, often makes the dynamic performance of urethane can not reach expected results.Japanese Patent Jap.Pat.No.28425., Jap.Pat.No.13880., Jap.Pat.No.162718. and United States Patent (USP) 4144395,4487853,4550194,5145883 adopt esterification process or adding micromolecule additive such as methods such as phosphide and small molecules prepolymer to make polyethers and pet reaction synthesizing polyether ester polyol respectively, but this method at polyether glycol terminal esterification modification often makes by products such as containing a certain amount of short chain polyester in the molecule, and the intensity of the urethane that obtains thus and tensile property are also relatively poor.
Summary of the invention:
The purpose of this invention is to provide a kind of easy to operate, the method for preparing polyester ether polylol of no coupling product.
Preparation method of the present invention comprises the steps:
Small molecules polyethers, cyclic acid anhydride and the catalyzer that will contain n reactive hydrogen atom are inserted in the autoclave by a certain percentage, vacuumize repeatedly and fill with nitrogen, add epoxide, polymerization 2～50 hours when being warmed up to 50～200 ℃;
Wherein each raw material consists of:
The mol ratio of epoxide and cyclic acid anhydride is an epoxide: cyclic acid anhydride=1.1～20: 1, and contain the small molecules polyethers of n reactive hydrogen atom and the mol ratio of cyclic acid anhydride and be: small molecules polyethers: cyclic acid anhydride=1: 0.5n～5n;
Catalyst levels accounts for 0.01～0.03% of small molecules polyethers, epoxide and cyclic acid anhydride weight sum.
Aforesaid catalyzer is the bimetallic cyanide complex catalyst that contriver king's heart certain herbaceous plants with big flowers, Kang Maoqing, Liu Xiaohua propose in patent CN1239680A, this double metal cyanide is meant to have (CN) b (A) c of Ma[M '] compound of d structure, wherein M, M ' are metal ions, and A is CN
-Other part in addition, a, b, c, d are coefficients, b＞c.This catalyzer preparation method is particularly seen CN1239680A.
Aforesaid small molecules polyethers is the alcohols with certain molecular weight that contains n reactive hydrogen atom, preferably contains 2～6 hydroxyls, and hydroxyl value is between 20～200.
Aforesaid cyclic acid anhydride can be Succinic anhydried, Pyroglutaric acid, MALEIC ANHYDRIDE or Tetra hydro Phthalic anhydride.
Aforesaid epoxide can be oxyethane, propylene oxide, butylene oxide ring-1, butylene oxide ring-2, oxidation iso-butylene or epoxy chloropropane.
The optimum mol ratio of aforesaid epoxide and cyclic acid anhydride is 1.1～5: 1.
The hydroxyl that polyester ether polylol comprises is positioned at chain end, and the contained hydroxyl value of per molecule (functionality) equals the reactive hydrogen atom number that comprises in the per molecule initiator.Therefore, adopt the initiator that contains different reactive hydrogen atom numbers can obtain the different polyester ether polylol of functionality respectively.Functionality is branched structure greater than 2 o'clock polymkeric substance.
With the content of ester units in the inventive method synthetic polymkeric substance, use
1The HNMR spectrometry is measured, and can approach alternating copolymer for 10～50% (mol) of molecular chain unit sum.
The present invention adopts the content of acid anhydride in the infrared tracking and measuring material of Fu Li leaf, infers reaction conversion ratio with this.Transformation efficiency of the present invention is greater than 95%.
The polymerization technique that the present invention adopts is easy, transformation efficiency height, good reproducibility, cost is low, and contains more ester units, and molecular weight and functionality can be regulated, can satisfy various service requirements, comprise the preparation of urethane etc., be the very strong novel method of a kind of practicality.
Embodiment:
Embodiment 1
The 10.0g Cobalt Potassium Cyanide is dissolved in the 200ml deionized water, makes 0.16mol/l hexacyanocobaltate acid potassium solution; The 20.0g zinc chloride is dissolved in the 40ml deionized water, makes the 3.67mol/l liquor zinci chloridi; Make the zinc hexacyanocobaltate precipitation at the following liquor zinci chloridi of vigorous stirring, hexacyanocobaltate acid potassium solution uniform mixing.Use deionized water wash 3 times after the precipitate and separate, each 200ml, the throw out after the washing is dried to constant weight under vacuum; Dried throw out is placed in the encloses container that is filled with ethylene glycol diethyl ether gas, and precipitation is placed to constant weight, obtains zinc hexacyanocobaltate ethylene glycol diethyl ether bimetal complex catalyst.
In 1 liter of autoclave of exsiccant, add 100g poly-cyclopropane ether dibasic alcohol (hydroxyl value 160), 42g Tetra hydro Phthalic anhydride and 0.03g zinc hexacyanocobaltate ethylene glycol diethyl ether bimetal complex catalyst respectively, behind the nitrogen replacement, the still temperature is transferred to 120 ℃, start induction stirring, inject the 142g propylene oxide after 2 hours, reacted 3 hours, decompression removes unreacted monomer and condensation product, the weight of record resulting polymers after the discharging.Make the polyether ester dibasic alcohol of hydroxyl value 55, productive rate 98%.
Embodiment 2:
In 1 liter of autoclave of exsiccant, add 100g poly-cyclopropane ether trivalent alcohol (hydroxyl value 160), 85g MALEIC ANHYDRIDE and 0.04g zinc hexacyanocobaltate ethylene glycol diethyl ether bimetal complex catalyst, behind the nitrogen replacement, the still temperature is transferred to 140 ℃, start induction stirring, inject the 60g epoxy chloropropane after 2 hours, reacted 10 hours, decompression removes unreacted monomer and condensation product, the weight of record resulting polymers after the discharging.Make the polyether ester trivalent alcohol of hydroxyl value 66, productive rate 100%.
Embodiment 3:
In 1 liter of autoclave of exsiccant, add 100g poly-cyclopropane ether tetravalent alcohol (hydroxyl value 160), 60g succinyl oxide and 0.05g zinc hexacyanocobaltate ethylene glycol diethyl ether bimetal complex catalyst, behind the nitrogen replacement, the still temperature is transferred to 160 ℃, start induction stirring, inject 20g propylene oxide and 40g oxyethane after 2 hours, reacted 24 hours, decompression removes unreacted monomer and condensation product, the weight of record resulting polymers after the discharging.Make the polyether ester tetravalent alcohol of hydroxyl value 80, productive rate 95%.
Embodiment 4:
In 1 liter of autoclave of exsiccant, add 100g oxyethane ether dibasic alcohol (hydroxyl value 160), 90g Pyroglutaric acid and 0.03g zinc hexacyanocobaltate ethylene glycol diethyl ether bimetal complex catalyst, behind the nitrogen replacement, the still temperature is transferred to 180 ℃, start induction stirring, inject 30g butylene oxide ring and 30g epoxy chloropropane after 2 hours, reacted 100 hours, decompression removes unreacted monomer and condensation product, the weight of record resulting polymers after the discharging.Make the polyether ester dibasic alcohol of hydroxyl value 57, productive rate 90%.
Comparative Examples:
In 1 liter of autoclave of exsiccant, press 15g glycerine and 0.0157g zinc hexacyanocobaltate ethylene glycol diethyl ether bimetal complex catalyst, behind the nitrogen replacement, the still temperature is transferred to 120 ℃, start induction stirring, back injection 142g propylene oxide heats up, react to constant voltage, decompression removes unreacted monomer and condensation product, the weight of record resulting polymers after the discharging.Make the polyether ester dibasic alcohol of hydroxyl value 56, productive rate 98%.
Claims (7)
1. the preparation method of a polyester ether polylol is characterized in that comprising the steps:
Small molecules polyethers, cyclic acid anhydride and the catalyzer that will contain n reactive hydrogen atom are inserted in the autoclave by a certain percentage, vacuumize repeatedly and fill with nitrogen, add epoxide, polymerization 2～50 hours when being warmed up to 50～200 ℃;
Wherein each raw material consists of:
The mol ratio of epoxide and cyclic acid anhydride is an epoxide: cyclic acid anhydride=1.1～20: 1, and contain the small molecules polyethers of several reactive hydrogen atoms and the mol ratio of MALEIC ANHYDRIDE and be: small molecules polyethers: MALEIC ANHYDRIDE=1: 0.5n-5n;
Catalyst levels accounts for 0.01～0.03% of small molecules polyethers, epoxide and cyclic acid anhydride weight sum.
2. the preparation method of a kind of polyester ether polylol as claimed in claim 1 is characterized in that described catalyzer is a bimetallic cyanide complex catalyst.Double metal cyanide has (CN) b (A) c of Ma[M '] compound of d structure, wherein M, M ' they are metal ions, A is CN
-Other part in addition, a, b, c, d are coefficients, b＞c.
3. the preparation method of a kind of polyester ether polylol as claimed in claim 1 is characterized in that described small molecules polyethers is that n is the polyethers of 2～6 reactive hydrogen atoms.
4. the preparation method of a kind of polyester ether polylol as claimed in claim 3 is characterized in that described small molecules polyethers is the alcohols of hydroxyl value between 20～200.
5. the preparation method of a kind of polyester ether polylol as claimed in claim 1 is characterized in that described cyclic acid anhydride is Succinic anhydried, Pyroglutaric acid, MALEIC ANHYDRIDE or Tetra hydro Phthalic anhydride.
6. the preparation method of a kind of polyester ether polylol as claimed in claim 1 is characterized in that described epoxide is oxyethane, propylene oxide, butylene oxide ring-1, butylene oxide ring-2 or epoxy chloropropane, and their mixture.
7. the preparation method of a kind of polyester ether polylol as claimed in claim 1, the mol ratio that it is characterized in that described epoxide and cyclic acid anhydride is 1.1～5: 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB011304669A CN1176970C (en) | 2001-11-19 | 2001-11-19 | Method for preparing polyether ester polyalcohol |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB011304669A CN1176970C (en) | 2001-11-19 | 2001-11-19 | Method for preparing polyether ester polyalcohol |
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| Publication Number | Publication Date |
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| CN1431240A true CN1431240A (en) | 2003-07-23 |
| CN1176970C CN1176970C (en) | 2004-11-24 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB011304669A Expired - Fee Related CN1176970C (en) | 2001-11-19 | 2001-11-19 | Method for preparing polyether ester polyalcohol |
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| CN (1) | CN1176970C (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100491441C (en) * | 2006-11-10 | 2009-05-27 | 中国科学院山西煤炭化学研究所 | Method for preparing aliphatic oligo carbonate polyol |
| CN100500735C (en) * | 2007-04-13 | 2009-06-17 | 中国科学院山西煤炭化学研究所 | Production of fatty oligo-ester carbonate polyhydric alcohol |
| CN101089028B (en) * | 2006-06-15 | 2011-11-09 | 深圳市海川实业股份有限公司 | Process of preparing oxyalkylene-base unsaturated ester polymer |
| CN103525353A (en) * | 2012-07-01 | 2014-01-22 | 万华化学（北京）有限公司 | Polyurethane complex film adhesive and preparation method thereof |
| CN104072745A (en) * | 2014-07-04 | 2014-10-01 | 山东一诺威新材料有限公司 | Method for preparing polyether polyol for aromatic coating |
| CN105504259A (en) * | 2015-12-29 | 2016-04-20 | 浙江华峰新材料股份有限公司 | Polyurethane resin, preparation method thereof and application thereof to micro cellular elastomer |
| CN106414551A (en) * | 2014-01-06 | 2017-02-15 | 英威达技术有限公司 | Copolyether ester polyol process |
| CN107406571A (en) * | 2015-04-08 | 2017-11-28 | 国际壳牌研究有限公司 | Improvement on polyalcohol and polyurethanes |
| CN110511717A (en) * | 2019-10-12 | 2019-11-29 | 广东莱尔新材料科技股份有限公司 | A kind of wafer with protection film adhesive and preparation method thereof |
| CN114369236A (en) * | 2021-11-30 | 2022-04-19 | 山东一诺威新材料有限公司 | High-performance polyester ether polyol and preparation method and application thereof |
-
2001
- 2001-11-19 CN CNB011304669A patent/CN1176970C/en not_active Expired - Fee Related
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101089028B (en) * | 2006-06-15 | 2011-11-09 | 深圳市海川实业股份有限公司 | Process of preparing oxyalkylene-base unsaturated ester polymer |
| CN100491441C (en) * | 2006-11-10 | 2009-05-27 | 中国科学院山西煤炭化学研究所 | Method for preparing aliphatic oligo carbonate polyol |
| CN100500735C (en) * | 2007-04-13 | 2009-06-17 | 中国科学院山西煤炭化学研究所 | Production of fatty oligo-ester carbonate polyhydric alcohol |
| CN103525353A (en) * | 2012-07-01 | 2014-01-22 | 万华化学（北京）有限公司 | Polyurethane complex film adhesive and preparation method thereof |
| CN106414551A (en) * | 2014-01-06 | 2017-02-15 | 英威达技术有限公司 | Copolyether ester polyol process |
| TWI646125B (en) * | 2014-01-06 | 2019-01-01 | 盧森堡商英威達技術有限公司 | Copolyether ester polyol process |
| CN106414551B (en) * | 2014-01-06 | 2019-03-05 | 英威达技术有限公司 | Copolyether ester polyxol method |
| CN104072745A (en) * | 2014-07-04 | 2014-10-01 | 山东一诺威新材料有限公司 | Method for preparing polyether polyol for aromatic coating |
| CN107406571A (en) * | 2015-04-08 | 2017-11-28 | 国际壳牌研究有限公司 | Improvement on polyalcohol and polyurethanes |
| CN105504259A (en) * | 2015-12-29 | 2016-04-20 | 浙江华峰新材料股份有限公司 | Polyurethane resin, preparation method thereof and application thereof to micro cellular elastomer |
| CN110511717A (en) * | 2019-10-12 | 2019-11-29 | 广东莱尔新材料科技股份有限公司 | A kind of wafer with protection film adhesive and preparation method thereof |
| CN110511717B (en) * | 2019-10-12 | 2021-05-04 | 广东莱尔新材料科技股份有限公司 | Adhesive for wafer protective film and preparation method thereof |
| CN114369236A (en) * | 2021-11-30 | 2022-04-19 | 山东一诺威新材料有限公司 | High-performance polyester ether polyol and preparation method and application thereof |
| CN114369236B (en) * | 2021-11-30 | 2024-04-12 | 山东一诺威新材料有限公司 | High-performance polyester ether polyol, and preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1176970C (en) | 2004-11-24 |
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Granted publication date: 20041124 |