GB1285340A - Process for the manufacture of polyesters and polyurethane foams - Google Patents

Process for the manufacture of polyesters and polyurethane foams

Info

Publication number
GB1285340A
GB1285340A GB38973/69A GB3897369A GB1285340A GB 1285340 A GB1285340 A GB 1285340A GB 38973/69 A GB38973/69 A GB 38973/69A GB 3897369 A GB3897369 A GB 3897369A GB 1285340 A GB1285340 A GB 1285340A
Authority
GB
United Kingdom
Prior art keywords
epsilon
acid
mixture
oxycaproyl
polyester
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB38973/69A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Inter Polymer Research Corp
Original Assignee
Inter Polymer Research Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Inter Polymer Research Corp filed Critical Inter Polymer Research Corp
Publication of GB1285340A publication Critical patent/GB1285340A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4266Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
    • C08G18/4286Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones prepared from a combination of hydroxycarboxylic acids and/or lactones with polycarboxylic acids or ester forming derivatives thereof and polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/06Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/60Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

1285340 Liquid polyesters; polyurethanes INTER-POLYMER RESEARCH CORP 4 Aug 1969 [14 Aug 1968] 38973/69 Headings C3C and C3R A polyester which is liquid at 20-30‹ C. and which contains 10 to 70% by weight of the epsilon-oxycaproyl unit [-O-(CH 2 ) 5 -C(O)-] is prepared by reacting a material which will provide the epsilon-oxycaproyl unit with a dicarboxylic acid or anhydride, a glycol and a triol or tetrol, the proportions of the reactants being such that the resultant polyester has the required content of epsilon-oxycaproyl units. The epsilon-oxycaproyl units may be supplied by epsilon caprolactone or by 6-hydroxycaproic acid or an oligomer thereof. The dicarboxylic acid or anhydride may be adipic acid, succinic acid, glutaric acid, pimelic acid, azelaic acid, an anhydride or mixture thereof, and the glycol may be ethylene, propylene, diethylene, dipropylene, 1,3-butylene or neopentylene glycol. The triol or tetrol may be glycerol, 1,2,6- hexanetriol, trimethylolpropane, pentaerythritol or alpha-methylglucoside, and is preferably used in an amount of 0À1 to 5 weight per cent based on the total reactants. The reaction is preferably carried out in the presence of 5 parts per million to 0À3 weight per cent of an esterinterchange or polyesterification catalyst, and at a temperature of 100‹ to 300‹ C. A flexible polyurethane is prepared by reacting a polyester of the invention with at least one organic polyisocyanate, at least one blowing agent, at least one catalyst, and a surfactant. The polyisocyanate may be 2,4- or 2,6-toluene diisocyanate or a mixture thereof, a diphenylmethane diisocyanate, a polymeric condensation product of formaldehyde and aniline or orthotoluidine or a mixture of a diphenylmethane diisocyanate with its carbodiimide. The blowing agent may be water, a halogenated aliphatic hydrocarbon having a boiling point of - 40‹ to 70‹ C., a low-boiling hydrocarbon, carbon dioxide or a mixture of water with one of the other blowing agents. The catalyst may be a tertiary amine, a metallic catalyst or a mixture thereof. When the polyester contains 35 to 72% of the epsilon-oxycaproyl unit, the surfactant may be a siloxane-oxyalkylene copolymer containing 15- 30% of the polysiloxane, and when the polyester contains 10 to 35% of the epsilon-oxycaproyl unit, the surfactant may be a polyoxypropylene-polyoxyethylene copolymer, a nonylphenol-ethylene oxide adduct, an alkoxysilane, a polysilyl phosphonate, a polydimethylsiloxane, a metal soap or an alkali metal sulphonate.
GB38973/69A 1968-08-14 1969-08-04 Process for the manufacture of polyesters and polyurethane foams Expired GB1285340A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US75251368A 1968-08-14 1968-08-14

Publications (1)

Publication Number Publication Date
GB1285340A true GB1285340A (en) 1972-08-16

Family

ID=25026624

Family Applications (1)

Application Number Title Priority Date Filing Date
GB38973/69A Expired GB1285340A (en) 1968-08-14 1969-08-04 Process for the manufacture of polyesters and polyurethane foams

Country Status (8)

Country Link
JP (1) JPS5022079B1 (en)
BE (1) BE737483A (en)
CH (1) CH523296A (en)
DE (1) DE1940942A1 (en)
ES (2) ES370475A1 (en)
FR (1) FR2015687A1 (en)
GB (1) GB1285340A (en)
ZA (1) ZA695568B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2545093A2 (en) * 2010-03-12 2013-01-16 Synthezyme LLC Polyurethane polymers comprising copolyester polyols having repeat units derived from biobased -hydroxyfatty acids
WO2014041486A1 (en) * 2012-09-11 2014-03-20 Halil Murat Aydin Biodegradable elastomer and a production method thereof
CN112111051A (en) * 2020-08-18 2020-12-22 青岛科技大学 Synthesis process of caprolactone oligomer

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5963535A (en) * 1982-10-04 1984-04-11 Nippon Denso Co Ltd Temperature sensor
JPH09249477A (en) * 1996-03-14 1997-09-22 Yuukishitsu Hiryo Seibutsu Kassei Riyou Gijutsu Kenkyu Kumiai Granular fertilizer coated with collapsible coating film

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2545093A2 (en) * 2010-03-12 2013-01-16 Synthezyme LLC Polyurethane polymers comprising copolyester polyols having repeat units derived from biobased -hydroxyfatty acids
EP2545093A4 (en) * 2010-03-12 2015-01-21 Synthezyme Llc Polyurethane polymers comprising copolyester polyols having repeat units derived from biobased -hydroxyfatty acids
WO2014041486A1 (en) * 2012-09-11 2014-03-20 Halil Murat Aydin Biodegradable elastomer and a production method thereof
CN112111051A (en) * 2020-08-18 2020-12-22 青岛科技大学 Synthesis process of caprolactone oligomer

Also Published As

Publication number Publication date
JPS5022079B1 (en) 1975-07-28
ZA695568B (en) 1971-06-30
BE737483A (en) 1970-02-16
ES370475A1 (en) 1971-07-16
ES391281A1 (en) 1973-07-01
FR2015687A1 (en) 1970-04-30
CH523296A (en) 1972-05-31
DE1940942A1 (en) 1970-08-06

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees