GB1499447A - Process for the preparation of materials comprising a polyurethane cellular layer - Google Patents

Process for the preparation of materials comprising a polyurethane cellular layer

Info

Publication number
GB1499447A
GB1499447A GB4691175A GB4691175A GB1499447A GB 1499447 A GB1499447 A GB 1499447A GB 4691175 A GB4691175 A GB 4691175A GB 4691175 A GB4691175 A GB 4691175A GB 1499447 A GB1499447 A GB 1499447A
Authority
GB
United Kingdom
Prior art keywords
prepolymer
polyurethane
compositions
prepared
catalyst
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
GB4691175A
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.)
Rhone Poulenc Industries SA
Original Assignee
Rhone Poulenc Industries SA
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 Rhone Poulenc Industries SA filed Critical Rhone Poulenc Industries SA
Publication of GB1499447A publication Critical patent/GB1499447A/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
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step

Abstract

1499447 Materials comprising a polyurethane cellular layer RHONE-POULENC INDUSTRIES 13 Nov 1975 [18 Dec 1974] 46911/75 Heading C3R [Also in Division B2] A process for the preparation of a material comprising a polyurethane cellular layer comprises (a) coating the material with a polyurethane-based expandable composition comprising a polyurethane prepolymer possessing terminal NCO groups and a catalyst for the formation of carbodiimide groups, the prepolymer having been prepared by the reaction of a polyisocyanate with a polyol having an average molecular weight per OH group of 200 to 6000, the polyol having an average number of functional groups of at most equal to 3, the said catalyst being present in an amount from 0À1 to 15% wt. of the prepolymer, and (b) heat treating the coated material at 100‹ to 180‹ C. to cause expansion and cross-linking of the polymer. The catalyst is preferably a phospholine or phospholidine or a sulphide or oxide thereof or a 2,4,6-tri-(dialkanolamine)-triazine. Suitable polyols include diethylene glycol, dipropylene glycol; polyhydroxylic polyethers or polyesters; α,# - dihydroxy - polyesteramides, polyurethanes and hydrocarbons; optionally modified castor oil, and etherified silanols or siloxanes. Suitable polyisocyanates include any aliphatic, cycloaliphatic or aromatic diisocyanate, a diisocyanate/monomeric polyol reaction product or an NCO-terminated polyurethane prepolymer. The catalyst system for the preparation of the prepolymer may be based on malonitrile, an alkali metal hydroxide or tertiary amine and a compound of a metal selected from Co, Sn, Pb, Bi, Fe and Zn. The compositions may comprise 10-200% wt. of fillers and 1-50% wt. of plasticizers based on the weight of the prepolymer, as well as surface-active agents; blowing agents, e.g. water, volatile hydrocarbons or halocarbons; heat stabilizers; flameproofing agents; U.V. absorbers; dyes and pigments. The compositions can be used for coating textiles particularly for coating carpet backings. In the examples, compositions are prepared by mixing (A) an NCO-terminated prepolymer prepared by reacting (1) either a polyether prepared by condensing propylene oxide and ethylene oxide on glycerol or (2) polyoxypropylene glycol and glycerol, with an 80/20 mixture of 2,4- and 2,6-toluene diisocyanate in the presence of aqueous KOH, malonitrile and dibutyltin dilaurate, with (B) 3 - methyl - 1 - phenyl - 1 - phosphocyclopent- 3-ene oxide dissolved in hexamethylphosphotriamide, a silicone/glycol copolymer surface active agent, and optionally either a mixture of calcined clay and rutile titanium oxide, or talc. The compositions are coated on to a tufted carpet and heated at 160‹ C. to form a cellular polyurethane layer on the backing of the carpet.
GB4691175A 1974-12-18 1975-11-13 Process for the preparation of materials comprising a polyurethane cellular layer Expired GB1499447A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7441765A FR2295075A1 (en) 1974-12-18 1974-12-18 EXPANDABLE COMPOSITIONS BASED ON POLYURETHANE

Publications (1)

Publication Number Publication Date
GB1499447A true GB1499447A (en) 1978-02-01

Family

ID=9146342

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4691175A Expired GB1499447A (en) 1974-12-18 1975-11-13 Process for the preparation of materials comprising a polyurethane cellular layer

Country Status (7)

Country Link
JP (1) JPS5337278B2 (en)
BE (1) BE836758A (en)
DE (1) DE2556810C3 (en)
FR (1) FR2295075A1 (en)
GB (1) GB1499447A (en)
IT (1) IT1058329B (en)
NL (1) NL7514397A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013134247A1 (en) * 2012-03-06 2013-09-12 Basf Se Method of producing a flexible polyurethane foam article

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8902228D0 (en) * 1989-02-01 1989-03-22 Ici Plc Carbodiimide-isocyanurate rigid foams
CN112897543B (en) * 2019-12-04 2023-01-06 中国石油天然气股份有限公司 Method for reducing particle size of kaolin fine powder

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2853518A (en) * 1956-07-30 1958-09-23 Du Pont Chemical process
MX150388A (en) * 1969-01-31 1984-04-30 Union Carbide Corp IMPROVED PROCEDURE TO PROVIDE A SECOND BACKUP ON CARPETING MATERIAL
US3645923A (en) * 1970-01-26 1972-02-29 Basf Wyandotte Corp Carbodiimide foam composition and process for the preparation therefor
US3994837A (en) * 1974-10-02 1976-11-30 Basf Wyandotte Corporation Urethane-modified carbodiimide-isocynurate foams prepared from TDI-rich isocyanates

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013134247A1 (en) * 2012-03-06 2013-09-12 Basf Se Method of producing a flexible polyurethane foam article
US10329398B2 (en) 2012-03-06 2019-06-25 Basf Se Method of producing a flexible polyurethane foam article

Also Published As

Publication number Publication date
DE2556810B2 (en) 1980-10-23
NL7514397A (en) 1976-06-22
DE2556810A1 (en) 1976-06-24
JPS5186595A (en) 1976-07-29
FR2295075B1 (en) 1978-02-24
IT1058329B (en) 1982-04-10
DE2556810C3 (en) 1981-09-17
BE836758A (en) 1976-06-17
JPS5337278B2 (en) 1978-10-07
FR2295075A1 (en) 1976-07-16

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee