NO833331L - Umettede ureidpolymerer, samt fremgangsmaate ved fremstilling derav - Google Patents

Umettede ureidpolymerer, samt fremgangsmaate ved fremstilling derav

Info

Publication number: NO833331L
Authority: NO; Norway
Prior art keywords: polymer; alpha; beta unsaturated; reactant; polymers
Prior art date: 1982-09-16

Application number

NO833331A

Other languages

English (en)

Norwegian (no)

Inventor

Fernando E Blanco

Original Assignee

Prod Res & Chem 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.)

1982-09-16

Filing date

1983-09-15

Publication date

1984-03-19

1982-09-16 Priority claimed from US06/418,667 external-priority patent/US4426506A/en

1983-09-15 Application filed by Prod Res & Chem Corp filed Critical Prod Res & Chem Corp

1984-03-19 Publication of NO833331L publication Critical patent/NO833331L/no

Links

229920000642 polymer Polymers 0.000 title claims abstract description 71
238000000034 method Methods 0.000 title claims description 8
238000002360 preparation method Methods 0.000 title description 5
229920006395 saturated elastomer Polymers 0.000 title 1
238000006243 chemical reaction Methods 0.000 claims abstract description 21
239000007788 liquid Substances 0.000 claims abstract description 20
150000001408 amides Chemical class 0.000 claims abstract description 19
150000007945 N-acyl ureas Chemical class 0.000 claims abstract description 15
239000001257 hydrogen Substances 0.000 claims abstract description 10
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 10
125000000217 alkyl group Chemical group 0.000 claims abstract description 9
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 8
239000000203 mixture Substances 0.000 claims abstract description 7
229910052736 halogen Inorganic materials 0.000 claims abstract description 6
150000002367 halogens Chemical class 0.000 claims abstract description 6
238000010438 heat treatment Methods 0.000 claims abstract description 3
239000000376 reactant Substances 0.000 claims abstract 10
150000002431 hydrogen Chemical class 0.000 claims abstract 4
239000012948 isocyanate Substances 0.000 claims description 15
150000002513 isocyanates Chemical class 0.000 claims description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 6
239000005062 Polybutadiene Substances 0.000 claims description 5
229920002857 polybutadiene Polymers 0.000 claims description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
239000011541 reaction mixture Substances 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
229910052794 bromium Inorganic materials 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
-1 acrylyl Chemical group 0.000 description 17
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
239000002243 precursor Substances 0.000 description 8
229920001971 elastomer Polymers 0.000 description 7
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 7
229920001451 polypropylene glycol Polymers 0.000 description 7
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 6
239000003054 catalyst Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000000047 product Substances 0.000 description 4
239000005060 rubber Substances 0.000 description 4
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000806 elastomer Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
239000000463 material Substances 0.000 description 3
239000000178 monomer Substances 0.000 description 3
229920001021 polysulfide Polymers 0.000 description 3
229920006295 polythiol Polymers 0.000 description 3
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
150000004678 hydrides Chemical class 0.000 description 2
239000000575 pesticide Substances 0.000 description 2
239000004033 plastic Substances 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
230000009257 reactivity Effects 0.000 description 2
239000000565 sealant Substances 0.000 description 2
229920003002 synthetic resin Polymers 0.000 description 2
239000000057 synthetic resin Substances 0.000 description 2
YBXYCBGDIALKAK-UHFFFAOYSA-N 2-chloroprop-2-enamide Chemical compound NC(=O)C(Cl)=C YBXYCBGDIALKAK-UHFFFAOYSA-N 0.000 description 1
LPNSCOVIJFIXTJ-UHFFFAOYSA-N 2-methylidenebutanamide Chemical compound CCC(=C)C(N)=O LPNSCOVIJFIXTJ-UHFFFAOYSA-N 0.000 description 1
GASMGDMKGYYAHY-UHFFFAOYSA-N 2-methylidenehexanamide Chemical compound CCCCC(=C)C(N)=O GASMGDMKGYYAHY-UHFFFAOYSA-N 0.000 description 1
SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001336 alkenes Chemical group 0.000 description 1
125000006177 alkyl benzyl group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
UCVPKAZCQPRWAY-UHFFFAOYSA-N dibenzyl benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC=2C=CC=CC=2)C=1C(=O)OCC1=CC=CC=C1 UCVPKAZCQPRWAY-UHFFFAOYSA-N 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
239000010985 leather Substances 0.000 description 1
239000011344 liquid material Substances 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
239000005077 polysulfide Substances 0.000 description 1
150000008117 polysulfides Polymers 0.000 description 1
229920013730 reactive polymer Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
239000004753 textile Substances 0.000 description 1
DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
ZFNFNJYRZOQPJF-UHFFFAOYSA-N trimethoxy(sulfanyl)silane Chemical compound CO[Si](S)(OC)OC ZFNFNJYRZOQPJF-UHFFFAOYSA-N 0.000 description 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
238000009849 vacuum degassing Methods 0.000 description 1
238000004073 vulcanization Methods 0.000 description 1

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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- 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
- C08G18/83—Chemically modified polymers
- C08G18/833—Chemically modified polymers by nitrogen containing compounds
- 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
- C08G18/83—Chemically modified polymers
- C08G18/834—Chemically modified polymers by compounds containing a thiol group
- C08G18/835—Unsaturated polymers modified by compounds containing a thiol group
- 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
- C08G18/83—Chemically modified polymers
- C08G18/837—Chemically modified polymers by silicon containing compounds

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polyurethanes Or Polyureas (AREA)

NO833331A 1982-09-16 1983-09-15 Umettede ureidpolymerer, samt fremgangsmaate ved fremstilling derav NO833331L (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/418,667 US4426506A (en)	1982-09-16	1982-09-16	Alpha-beta unsaturated ureide polymers, method for making same and cured elastomers produced therefrom
US50474083A	1983-06-16	1983-06-16

Publications (1)

Publication Number	Publication Date
NO833331L true NO833331L (no)	1984-03-19

Family

ID=27024221

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO833331A NO833331L (no)	1982-09-16	1983-09-15	Umettede ureidpolymerer, samt fremgangsmaate ved fremstilling derav

Country Status (7)

Country	Link
EP (1)	EP0104035A3 (da)
AU (1)	AU1910483A (da)
BR (1)	BR8304996A (da)
CA (1)	CA1213396A (da)
DK (1)	DK420183A (da)
ES (1)	ES8503013A1 (da)
NO (1)	NO833331L (da)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0204497B1 (en) *	1985-05-28	1994-07-13	Nippon Paint Co., Ltd.	Polymerisation process employing compounds having polymerisable acylurethane structures
GB2334260A (en) *	1996-12-06	1999-08-18	Smith & Nephew	Adhesives
GB9625422D0 (en) *	1996-12-06	1997-01-22	Smith & Nephew	Adhesives

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB820005A (en) *	1956-08-15	1959-09-16	Us Rubber Co	Improvements in polyurethane elastomers and method of making the same
GB1352063A (en) *	1971-01-08	1974-05-15	Ici Ltd	Polymerisable compositions and resins derived thererom
US4439576A (en) *	1980-11-03	1984-03-27	Olin Corporation	Modified polyurethane liquid polymer compositions

1983
- 1983-08-25 CA CA000435373A patent/CA1213396A/en not_active Expired
- 1983-09-09 EP EP83305291A patent/EP0104035A3/en not_active Withdrawn
- 1983-09-14 AU AU19104/83A patent/AU1910483A/en not_active Abandoned
- 1983-09-15 BR BR8304996A patent/BR8304996A/pt unknown
- 1983-09-15 NO NO833331A patent/NO833331L/no unknown
- 1983-09-15 DK DK420183A patent/DK420183A/da not_active Application Discontinuation
- 1983-09-15 ES ES525628A patent/ES8503013A1/es not_active Expired

Also Published As

Publication number	Publication date
AU1910483A (en)	1984-03-22
BR8304996A (pt)	1984-09-04
ES525628A0 (es)	1985-02-01
DK420183D0 (da)	1983-09-15
EP0104035A2 (en)	1984-03-28
CA1213396A (en)	1986-10-28
ES8503013A1 (es)	1985-02-01
DK420183A (da)	1984-03-17
EP0104035A3 (en)	1985-04-03

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