SE366325B - - Google Patents

Info

Publication number: SE366325B
Authority: SE; Sweden
Prior art keywords: diisocyanate; ethylene; polymer; cross; nitrated
Prior art date: 1968-08-30

Application number

SE11903/69A

Other languages

English (en)

Inventor

D Magay

Original Assignee

Raychem 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.)

1968-08-30

Filing date

1969-08-28

Publication date

1974-04-22

1969-08-28 Application filed by Raychem Corp filed Critical Raychem Corp

1974-04-22 Publication of SE366325B publication Critical patent/SE366325B/xx

Links

229920000642 polymer Polymers 0.000 abstract 10
229920001577 copolymer Polymers 0.000 abstract 6
-1 hydrogen compound Chemical class 0.000 abstract 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 5
ICLCCFKUSALICQ-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanato-3-methylphenyl)-2-methylbenzene Chemical compound C1=C(N=C=O)C(C)=CC(C=2C=C(C)C(N=C=O)=CC=2)=C1 ICLCCFKUSALICQ-UHFFFAOYSA-N 0.000 abstract 4
239000005057 Hexamethylene diisocyanate Substances 0.000 abstract 4
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 abstract 4
239000005056 polyisocyanate Substances 0.000 abstract 4
229920001228 polyisocyanate Polymers 0.000 abstract 4
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 abstract 3
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 3
239000005977 Ethylene Substances 0.000 abstract 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
239000004698 Polyethylene Substances 0.000 abstract 3
239000003054 catalyst Substances 0.000 abstract 3
229920000573 polyethylene Polymers 0.000 abstract 3
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 abstract 3
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 2
QZWKEPYTBWZJJA-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine-4,4'-diisocyanate Chemical compound C1=C(N=C=O)C(OC)=CC(C=2C=C(OC)C(N=C=O)=CC=2)=C1 QZWKEPYTBWZJJA-UHFFFAOYSA-N 0.000 abstract 2
238000004132 cross linking Methods 0.000 abstract 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
VYXHVRARDIDEHS-QGTKBVGQSA-N (1z,5z)-cycloocta-1,5-diene Chemical compound C\1C\C=C/CC\C=C/1 VYXHVRARDIDEHS-QGTKBVGQSA-N 0.000 abstract 1
XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 abstract 1
MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 abstract 1
238000005698 Diels-Alder reaction Methods 0.000 abstract 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 abstract 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 1
229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 abstract 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
150000001298 alcohols Chemical class 0.000 abstract 1
150000001412 amines Chemical class 0.000 abstract 1
229910000410 antimony oxide Inorganic materials 0.000 abstract 1
150000001721 carbon Chemical group 0.000 abstract 1
229910052799 carbon Inorganic materials 0.000 abstract 1
125000004432 carbon atom Chemical group C* 0.000 abstract 1
239000006229 carbon black Substances 0.000 abstract 1
238000006243 chemical reaction Methods 0.000 abstract 1
239000011248 coating agent Substances 0.000 abstract 1
238000000576 coating method Methods 0.000 abstract 1
238000013329 compounding Methods 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
125000005442 diisocyanate group Chemical group 0.000 abstract 1
VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical compound ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 0.000 abstract 1
PZDUWXKXFAIFOR-UHFFFAOYSA-N hexadecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C=C PZDUWXKXFAIFOR-UHFFFAOYSA-N 0.000 abstract 1
150000002483 hydrogen compounds Chemical class 0.000 abstract 1
239000004615 ingredient Substances 0.000 abstract 1
239000007788 liquid Substances 0.000 abstract 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 abstract 1
239000000395 magnesium oxide Substances 0.000 abstract 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
239000000391 magnesium silicate Substances 0.000 abstract 1
229910052919 magnesium silicate Inorganic materials 0.000 abstract 1
235000019792 magnesium silicate Nutrition 0.000 abstract 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 abstract 1
239000000203 mixture Substances 0.000 abstract 1
230000000802 nitrating effect Effects 0.000 abstract 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 abstract 1
239000012188 paraffin wax Substances 0.000 abstract 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract 1
229920001083 polybutene Polymers 0.000 abstract 1
238000011084 recovery Methods 0.000 abstract 1
239000007787 solid Substances 0.000 abstract 1
150000003512 tertiary amines Chemical class 0.000 abstract 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
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6283—Polymers of nitrogen containing compounds having carbon-to-carbon double bonds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L57/00—Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/02—Ethene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2810/00—Chemical modification of a polymer
- C08F2810/20—Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently

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)

SE11903/69A 1968-08-30 1969-08-28 SE366325B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US75642868A	1968-08-30	1968-08-30

Publications (1)

Publication Number	Publication Date
SE366325B true SE366325B (de)	1974-04-22

Family

ID=25043436

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE11903/69A SE366325B (de)	1968-08-30	1969-08-28

Country Status (8)

Country	Link
US (1)	US3583961A (de)
BE (1)	BE738223A (de)
CH (1)	CH533652A (de)
DE (1)	DE1944113A1 (de)
FR (1)	FR2017126A1 (de)
GB (1)	GB1258982A (de)
NL (1)	NL6913180A (de)
SE (1)	SE366325B (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL151996B (nl) *	1971-04-15	1977-01-17	Snam Progetti	Werkwijze voor de bereiding van gemodificeerde polymeren.
US3879358A (en) *	1971-05-28	1975-04-22	Texaco Inc	Nitrated polymers with saturated hydrocarbon backbone
AU7496074A (en) *	1973-11-21	1976-05-06	Snam Progetti	Transforming hydrocarbon polymers into photodegradable
CA1267419A (en) *	1982-07-15	1990-04-03	Ross Wood Millar	Process for the production of high energy material
GB9406481D0 (en)	1994-03-31	1994-05-25	Central Research Lab Ltd	Border for an image
US8431060B2 (en)	2006-01-31	2013-04-30	Abbott Cardiovascular Systems Inc.	Method of fabricating an implantable medical device using gel extrusion and charge induced orientation
US9492587B2 (en) *	2009-04-13	2016-11-15	Abbott Cardiovascular Systems Inc.	Stent made from an ultra high molecular weight bioabsorbable polymer with high fatigue and fracture resistance
US8841412B2 (en)	2011-08-11	2014-09-23	Abbott Cardiovascular Systems Inc.	Controlling moisture in and plasticization of bioresorbable polymer for melt processing

1968
- 1968-08-30 US US756428A patent/US3583961A/en not_active Expired - Lifetime
1969
- 1969-08-28 GB GB1258982D patent/GB1258982A/en not_active Expired
- 1969-08-28 SE SE11903/69A patent/SE366325B/xx unknown
- 1969-08-28 NL NL6913180A patent/NL6913180A/xx unknown
- 1969-08-29 CH CH1317069A patent/CH533652A/de not_active IP Right Cessation
- 1969-08-29 BE BE738223D patent/BE738223A/xx not_active IP Right Cessation
- 1969-08-30 DE DE19691944113 patent/DE1944113A1/de active Pending
- 1969-09-01 FR FR6929856A patent/FR2017126A1/fr active Pending

Also Published As

Publication number	Publication date
GB1258982A (de)	1972-01-05
US3583961A (en)	1971-06-08
BE738223A (de)	1970-03-02
DE1944113A1 (de)	1970-08-27
FR2017126A1 (de)	1970-05-15
CH533652A (de)	1973-02-15
NL6913180A (de)	1970-03-03

Publication	Publication Date	Title
NL6913180A (de)	1970-03-03
EP0449143A2 (de)	1991-10-02	Bei niedrigen Temperaturen aktive aliphatische/aromatische Polycarbodiimide
GB1345269A (en)	1974-01-30	Acrylic urethane composition
GB1338002A (en)	1973-11-21	Process for the preparation of heterocyclic polymers
GB1519422A (en)	1978-07-26	Elastomers
KR940014533A (ko)	1994-07-18	방사선 경화성 폴리우레탄 에멀젼 조성물
US3265640A (en)	1966-08-09	Crosslinked polymers from alpha, alpha-dichloro-p-xylene and polysubstituted benzenes
GB1029086A (en)	1966-05-11	Process for the preparation of isocyanate polyaddition products
GB851773A (en)	1960-10-19	N-vinyl-x-alkyl-2-oxazolidinones and their polymers
US3219725A (en)	1965-11-23	Segmented oxymethylene block copolymers
US2324936A (en)	1943-07-20	Condensation of cyanocarboxylic acid with polyamine
GB1184893A (en)	1970-03-18	Foamed Polymers Containing an Isocyanurate Ring Structure
GB1022563A (en)	1966-03-16	Copolymers
US3766147A (en)	1973-10-16	Condensation of cyclic nitrile carbonates with fluoride compounds
US3466314A (en)	1969-09-09	Silicon compounds
GB1242911A (en)	1971-08-18	Improvements in and relating to the crosslinking of polymers
US3761453A (en)	1973-09-25	Nitroso perfluoro addition polymers
JPS6160093B2 (de)	1986-12-19
US3855332A (en)	1974-12-17	Process for production of polyarylenes
ES257503A1 (es)	1960-10-16	Un procedimiento para mejorar la receptividad al tinte de fibras a base de mezclas de resinas sinteticas con compuestos basicos
US3092612A (en)	1963-06-04	Copolymers preparation process
US2924579A (en)	1960-02-09	Method of preparing aluminum chloride complex catalyst
US2555500A (en)	1951-06-05	Copolymers of 4-vinylcyclohexene dioxide
JPS62225506A (ja)	1987-10-03	イソブチレン共重合体、その製法及び用途
Coutinho et al.	1988	Kinetic study of the reaction between a hydroxylated polybutadiene and isocyanates in chlorobenzene, III. Reaction with dimer diacid diisocyanate (DDI)