GB822546A - Cellular elastomeric materials - Google Patents

Cellular elastomeric materials

Info

Publication number
GB822546A
GB822546A GB1800755A GB1800755A GB822546A GB 822546 A GB822546 A GB 822546A GB 1800755 A GB1800755 A GB 1800755A GB 1800755 A GB1800755 A GB 1800755A GB 822546 A GB822546 A GB 822546A
Authority
GB
United Kingdom
Prior art keywords
hydroxy
cross
polyesters
groups
composition
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
GB1800755A
Inventor
Peter Merriman
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.)
Dunlop Rubber Co Ltd
Original Assignee
Dunlop Rubber Co Ltd
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
Priority to DENDAT1048407D priority Critical patent/DE1048407B/en
Application filed by Dunlop Rubber Co Ltd filed Critical Dunlop Rubber Co Ltd
Priority to GB1800755A priority patent/GB822546A/en
Priority to FR1159607D priority patent/FR1159607A/en
Publication of GB822546A publication Critical patent/GB822546A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/12Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

A method of producing cellular elastomeric materials comprises forming a liquid or plastic composition comprising a polymer containing isocyanate or isothiocyanate groups, a compound of molecular weight greater than 200 containing at least two groups capable of reacting with and cross-linking the polymer and an inert gas under pressure, foaming the composition by reducing the pressure thereon and subsequently setting the composition by furthering the condensation thereof before substantial breakdown of the foam occurs. As cross-linking agents there can be used organic poly-hydroxy compounds, diamines and aminoalcohols. Suitable polyhydroxy compounds are liquid hydroxy-polyesters, poly-(carboxy-/hydroxy-)-polyesters and hydroxy-polyethers. Preferably the hydroxy-polyesters, in addition to terminal or near-terminal hydroxy groups, contain one or more other intermediately-situated hydroxy or carboxy groups. Suitable esters can also be obtained by dehydration or blowing of vegetable oils, such as castor oil, which contain one or more hydroxy groups in the acid radical. The polycarbonates, such as can be obtained by phosgenation of glycols and other polyhydroxy compounds can also be used. The polymers containing isocyanate or isothiocyanate groups include reaction products of polyethers, polyesters or polyesteramides with a slight stoichiometrical excess of organic polyisocyanates or polyisothiocyanates. A liquefied gas and/or a volatile solvent may also be present in the starting materials. In examples: (1) a syrup obtained by reacting poly-ethylene glycol adipate and paraphenylene diisocyanate is stirred with a cross-linking agent comprising an adipic acid/polyethylene glycol/trimethylol propane reaction product while a mixture of triethylamine and an N-diethyl-ethanolamine/adipic acid reaction product is passed in through the stirrer. Concurrently carbon dioxide is fed in to give a working pressure of 200 lbs. sq. inch. The mixture then passes out to trays where it foams up and the foam is finally matured by heating; (2) a similar process employs an hydroxy-polycarbonate as the cross-linking agent. Specification 803,771 is referred to.ALSO:A method of producing cellular elastomeric materials comprises forming a liquid or plastic composition comprising a polymer containing isocyanate or isothiocyanate groups, a compound of molecular weight greater than 200 containing at least two groups capable or reacting with and cross-linking the polymer and an inert gas under pressure, foaming the composition by reducing the pressure thereon and subsequently setting the composition by furthering the condensation thereof, before substantial breakdown of the foam occurs. As cross-linking agents there can be used organic polyhydroxy compounds, diamines and amino-alcohols. Suitable polyhydroxy compounds are liquid hydroxypolyesters, poly (carboxy/hydroxy) polyesters and hydroxypolyethers. Suitable esters can also be obtained by dehydration or blowing of vegetable oils, such as castor oil, which contain one or more hydroxy groups in the acid radical. Polycarbonates such as can be obtained by phosgenation of glycols and other polyhydroxy compounds can also be used. The polymers containing isocyanate or isothiocyanate groups include reaction products of polyethers, polyesters or polyesteramides with excess polyisocyanate or polyisothiocyanate. A liquefied gas and/or a volatile solvent may also be present in the starting materials. In examples (1) a syrup obtained by reacting polyethylene glycol adipate and paraphenylene diisocyanate is stirred with a cross-lining agent comprising an adipic acid/polyethylene glycol/trimethylolpropane reaction product while a mixture of triethylamine and an N-diethylethanolamine/adipic acid reaction product is passed in through the stirrer. Concurrently carbon dioxide is fed in to give a working pressure of 200 lbs/sq. in. The mixture then passes out to trays where it foams up, and the foam is finally matured by heating; (2) a similar process employs a hydroxy-polycarbonate as the cross-linking agent. Specification 803,771 [Group IV(a)] is referred to.
GB1800755A 1955-06-22 1955-06-22 Cellular elastomeric materials Expired GB822546A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
DENDAT1048407D DE1048407B (en) 1955-06-22 Process for the production of elastic polyurethane foams
GB1800755A GB822546A (en) 1955-06-22 1955-06-22 Cellular elastomeric materials
FR1159607D FR1159607A (en) 1955-06-22 1956-06-14 Cellular elastomeric materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1800755A GB822546A (en) 1955-06-22 1955-06-22 Cellular elastomeric materials

Publications (1)

Publication Number Publication Date
GB822546A true GB822546A (en) 1959-10-28

Family

ID=10105029

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1800755A Expired GB822546A (en) 1955-06-22 1955-06-22 Cellular elastomeric materials

Country Status (3)

Country Link
DE (1) DE1048407B (en)
FR (1) FR1159607A (en)
GB (1) GB822546A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3256218A (en) * 1962-11-19 1966-06-14 Du Pont Dispersing coarse fillers in polyurethane foams
US3362919A (en) * 1965-02-04 1968-01-09 Pittsburgh Plate Glass Co Process for foaming thermoset organic materials
US3755212A (en) * 1971-05-13 1973-08-28 Dow Chemical Co Air blown polyurethane foams
US3849156A (en) * 1969-01-31 1974-11-19 Union Carbide Corp Process for providing a backing on carpets

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3108976A (en) * 1960-06-10 1963-10-29 Du Pont Preparation of a cured polyurethane cellular material
DE1144915B (en) * 1966-11-04 1963-03-07 Wolfen Filmfab Veb Process for the production of polyurethane foams
FR2981754B1 (en) 2011-10-24 2013-11-29 Renault Sa METHOD AND SYSTEM FOR DETERMINING THE CHARGE STATE OF AN ELEMENTARY CELL AND BATTERY

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3256218A (en) * 1962-11-19 1966-06-14 Du Pont Dispersing coarse fillers in polyurethane foams
US3362919A (en) * 1965-02-04 1968-01-09 Pittsburgh Plate Glass Co Process for foaming thermoset organic materials
US3849156A (en) * 1969-01-31 1974-11-19 Union Carbide Corp Process for providing a backing on carpets
US3755212A (en) * 1971-05-13 1973-08-28 Dow Chemical Co Air blown polyurethane foams

Also Published As

Publication number Publication date
FR1159607A (en) 1958-06-30
DE1048407B (en) 1959-01-08

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