GB1499447A - Process for the preparation of materials comprising a polyurethane cellular layer - Google Patents
Process for the preparation of materials comprising a polyurethane cellular layerInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
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)
- Carpets (AREA)
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.
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)
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)
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)
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 |
-
1974
- 1974-12-18 FR FR7441765A patent/FR2295075A1/en active Granted
-
1975
- 1975-11-13 GB GB4691175A patent/GB1499447A/en not_active Expired
- 1975-12-10 NL NL7514397A patent/NL7514397A/en not_active Application Discontinuation
- 1975-12-16 JP JP15009275A patent/JPS5337278B2/ja not_active Expired
- 1975-12-17 BE BE162847A patent/BE836758A/en not_active IP Right Cessation
- 1975-12-17 DE DE19752556810 patent/DE2556810C3/en not_active Expired
- 1975-12-18 IT IT3046675A patent/IT1058329B/en active
Cited By (2)
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 |
---|---|
FR2295075A1 (en) | 1976-07-16 |
FR2295075B1 (en) | 1978-02-24 |
JPS5186595A (en) | 1976-07-29 |
NL7514397A (en) | 1976-06-22 |
BE836758A (en) | 1976-06-17 |
DE2556810B2 (en) | 1980-10-23 |
DE2556810A1 (en) | 1976-06-24 |
JPS5337278B2 (en) | 1978-10-07 |
IT1058329B (en) | 1982-04-10 |
DE2556810C3 (en) | 1981-09-17 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |