GB967359A - Improvements in and relating to foamed polymers - Google Patents
Improvements in and relating to foamed polymersInfo
- Publication number
- GB967359A GB967359A GB3946160A GB3946160A GB967359A GB 967359 A GB967359 A GB 967359A GB 3946160 A GB3946160 A GB 3946160A GB 3946160 A GB3946160 A GB 3946160A GB 967359 A GB967359 A GB 967359A
- Authority
- GB
- United Kingdom
- Prior art keywords
- propylene oxide
- compounds
- nov
- ethylene
- propylene
- 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
- 229920000642 polymer Polymers 0.000 title abstract 3
- -1 heterocyclic radical Chemical group 0.000 abstract 8
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 abstract 2
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 abstract 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 229920005830 Polyurethane Foam Polymers 0.000 abstract 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 abstract 1
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 125000004653 anthracenylene group Chemical group 0.000 abstract 1
- 229910052787 antimony Inorganic materials 0.000 abstract 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 1
- 229910052785 arsenic Inorganic materials 0.000 abstract 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 abstract 1
- 229910052797 bismuth Inorganic materials 0.000 abstract 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 239000012975 dibutyltin dilaurate Substances 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 abstract 1
- 239000006260 foam Substances 0.000 abstract 1
- 238000005187 foaming Methods 0.000 abstract 1
- 239000004088 foaming agent Substances 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 1
- 150000007529 inorganic bases Chemical class 0.000 abstract 1
- 239000011133 lead Substances 0.000 abstract 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052753 mercury Inorganic materials 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical class C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 abstract 1
- 125000004957 naphthylene group Chemical group 0.000 abstract 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000007530 organic bases Chemical class 0.000 abstract 1
- 125000005562 phenanthrylene group Chemical group 0.000 abstract 1
- 229920000768 polyamine Polymers 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 239000011496 polyurethane foam Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000002562 thickening agent Substances 0.000 abstract 1
- 125000005309 thioalkoxy group Chemical group 0.000 abstract 1
- 125000005296 thioaryloxy group Chemical group 0.000 abstract 1
- 229910052719 titanium Inorganic materials 0.000 abstract 1
- 239000010936 titanium Substances 0.000 abstract 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 1
- 229940029284 trichlorofluoromethane Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
-
- 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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5033—Polyethers having heteroatoms other than oxygen having nitrogen containing carbocyclic groups
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/62—Alcohols or phenols
- C08G59/64—Amino alcohols
-
- 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
- C08G2101/00—Manufacture of cellular products
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/067—Polyaryl amine alkanes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polyethers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
967,359. Polyurethane foam. UNION CARBIDE CORPORATION. Nov. 17, 1960 [Nov. 20, 1959], No. 39461/60. Headings C3C and C3R. The invention comprises a foamed polymer containing within the polymer chain units of the formula in which X is an aromatic or heterocyclic radical, each R 4 is an ethylene or propylene radical, y is 2 or 3 and n is a whole number having a value of at least one. Radicals designated by X include phenylene, tolylene, phenenyl, naphthylene, anthrylene, phenanthrylene, polyvalent radicals derived from indene, indole, quinolinedibenzofuran, acenaphthene, fluorene; biphenylene; ring structures united through another group such as oxidiphenylene, thiodiphenylene, sulphenyldiphenylene, sulphonyldiphenylene, arylenediphenylene and azodiarylene. They may contain carboxyl, hydroxy, mercapto, alkoxy, halo, aryloxy, thioalkoxy, thioaryloxy, alkyl and alkenyl substituents. Polyamines containing such nuclei are listed. They are converted to polyhydroxy compounds by reaction with ethylene oxide or propylene oxide in amounts of from one to about 40 moles per hydroxyl group. One shot, prepolymer or semiprepolymer methods can be used in the foaming. Fluorocarbons can be used as foaming agents. Catalysts include inorganic and organic bases, compounds of arsenic, antimony, bismuth, titanium, lead, copper, and mercury, and stannous and organotin compounds. Clays thickening agents, powdered aluminium, diatomaceous earths, dyes and siloxane-oxyalkylene copolymers can also be present in the reaction mixture. In example (1) foam is prepared by agitating toluene 2,4- and 2,6-diisocyanates with a mixture of a propylene oxide addition product of 2,4-diaminotoluene, dibutyl tin dilaurate, silicone and trichloromonofluoromethane. In other examples reaction products of ethylene oxide and 2,4-toluenediamine and of propylene oxide and o- or pphenylenediamine, mixed 1,8- and 1,5-diaminonaphthalenes, 4,4<SP>1</SP>-diaminodiphenylmethane and 4,4',4<SP>11</SP>-methylidenetrianiline are used as starting materials. Specification 848,965 is referred to.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US577953A US2914556A (en) | 1956-04-13 | 1956-04-13 | Preparation of lactone adducts |
US85424459A | 1959-11-20 | 1959-11-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB967359A true GB967359A (en) | 1964-08-19 |
Family
ID=27077387
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1216357A Expired GB859643A (en) | 1956-04-13 | 1957-04-15 | Process for the preparation of lactone adducts and polyesters |
GB3946160A Expired GB967359A (en) | 1956-04-13 | 1960-11-17 | Improvements in and relating to foamed polymers |
GB3946060A Expired GB910333A (en) | 1956-04-13 | 1960-11-17 | Improvements in and relating to polymers |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1216357A Expired GB859643A (en) | 1956-04-13 | 1957-04-15 | Process for the preparation of lactone adducts and polyesters |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3946060A Expired GB910333A (en) | 1956-04-13 | 1960-11-17 | Improvements in and relating to polymers |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE556560A (en) |
DE (3) | DE1213995B (en) |
GB (3) | GB859643A (en) |
IT (1) | IT570070A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3423344A (en) * | 1963-12-30 | 1969-01-21 | Upjohn Co | Polyurethane polyol mixture containing hydroxyalkylated polyamines |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3314995A (en) * | 1963-12-09 | 1967-04-18 | Mobay Chemical Corp | Alkylene oxide adducts of bis(2, 4-diamino-5-methyl phenyl)methane |
US3293297A (en) * | 1964-07-30 | 1966-12-20 | Universal Oil Prod Co | Nu-oxyalkylated-aminediphenyl-oxo-and amino-compounds |
US3948825A (en) * | 1974-07-05 | 1976-04-06 | Basf Wyandotte Corporation | Curing agent for use in making cellular polyurethane compositions |
US4393199A (en) | 1981-05-12 | 1983-07-12 | S R I International | Cationic polymerization |
US4379914A (en) * | 1981-12-21 | 1983-04-12 | Exxon Research And Engineering Co. | Polycaprolactone polymers |
CN113166688B (en) * | 2018-12-13 | 2024-12-13 | 陶氏环球技术有限责任公司 | Liquid laundry detergent formulations |
WO2020123239A1 (en) * | 2018-12-13 | 2020-06-18 | Dow Global Technologies Llc | Cleaning booster |
CN116284735B (en) * | 2023-05-04 | 2023-12-29 | 辽宁奥克药业股份有限公司 | Catalyst for preparing block polyether and preparation method of block polyether |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR956245A (en) * | 1942-12-24 | 1950-01-27 | ||
DE878857C (en) * | 1943-06-26 | 1953-06-08 | Basf Ag | Process for the production of condensation products |
DE861609C (en) * | 1943-07-14 | 1953-01-05 | Basf Ag | Process for the production of high molecular weight condensation products |
GB776661A (en) * | 1954-01-28 | 1957-06-12 | Wyandotte Chemical Corp | Improved polyoxypropylene-polyoxyalkylene surface-active agents |
BE534967A (en) * | 1954-10-20 | |||
DE961573C (en) * | 1954-11-16 | 1957-04-11 | Bayer Ag | Process for the production of foams from linear or branched polyethers or polythioethers and polyisocyanates containing hydroxyl groups |
-
0
- IT IT570070D patent/IT570070A/it unknown
- BE BE556560D patent/BE556560A/xx unknown
-
1957
- 1957-04-09 DE DEU4474A patent/DE1213995B/en active Pending
- 1957-04-15 GB GB1216357A patent/GB859643A/en not_active Expired
-
1960
- 1960-11-14 DE DEU7577A patent/DE1151938B/en active Pending
- 1960-11-16 DE DEU7586A patent/DE1191098B/en active Pending
- 1960-11-17 GB GB3946160A patent/GB967359A/en not_active Expired
- 1960-11-17 GB GB3946060A patent/GB910333A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3423344A (en) * | 1963-12-30 | 1969-01-21 | Upjohn Co | Polyurethane polyol mixture containing hydroxyalkylated polyamines |
Also Published As
Publication number | Publication date |
---|---|
DE1213995B (en) | 1966-04-07 |
GB859643A (en) | 1961-01-25 |
DE1151938B (en) | 1963-07-25 |
DE1191098B (en) | 1965-04-15 |
BE556560A (en) | |
GB910333A (en) | 1962-11-14 |
IT570070A (en) |
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