JPS6363566B2 - - Google Patents

Info

Publication number: JPS6363566B2
Authority: JP; Japan
Prior art keywords: polyether; caprolactam; polyether prepolymer; lactam; block copolymer
Prior art date: 1983-11-22
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

JP22018583A

Other languages

English (en)

Japanese (ja)

Other versions

JPS60112825A (ja

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.)

1983-11-22

Filing date

1983-11-22

Publication date

1988-12-07

1983-11-22 Application filed filed Critical

1983-11-22 Priority to JP22018583A priority Critical patent/JPS60112825A/ja

1984-11-14 Priority to CA000467817A priority patent/CA1257028A/fr

1984-11-19 Priority to DE8484308009T priority patent/DE3485458D1/de

1984-11-19 Priority to EP84308009A priority patent/EP0147051B1/fr

1985-06-19 Publication of JPS60112825A publication Critical patent/JPS60112825A/ja

1986-10-02 Priority to US06/914,515 priority patent/US4792603A/en

1988-12-07 Publication of JPS6363566B2 publication Critical patent/JPS6363566B2/ja

Status Granted legal-status Critical Current

Links

239000004721 Polyphenylene oxide Substances 0.000 claims description 31
229920000570 polyether Polymers 0.000 claims description 31
229920006147 copolyamide elastomer Polymers 0.000 claims description 10
150000003951 lactams Chemical class 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
238000010539 anionic addition polymerization reaction Methods 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
239000002685 polymerization catalyst Substances 0.000 claims description 3
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 20
239000000203 mixture Substances 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 9
238000007711 solidification Methods 0.000 description 7
230000008023 solidification Effects 0.000 description 7
LBXFCUWIEJKZFT-UHFFFAOYSA-N 2-oxoazepane-1-carbonyl chloride Chemical compound ClC(=O)N1CCCCCC1=O LBXFCUWIEJKZFT-UHFFFAOYSA-N 0.000 description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
229920001451 polypropylene glycol Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
229920005989 resin Polymers 0.000 description 6
238000000034 method Methods 0.000 description 5
239000011259 mixed solution Substances 0.000 description 5
230000000704 physical effect Effects 0.000 description 5
238000003756 stirring Methods 0.000 description 5
YIFCDKDXYUCWAZ-UHFFFAOYSA-L magnesium;azepan-2-one;dibromide Chemical compound [Mg+2].[Br-].[Br-].O=C1CCCCCN1 YIFCDKDXYUCWAZ-UHFFFAOYSA-L 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
239000003513 alkali Substances 0.000 description 3
150000001450 anions Chemical class 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000012661 block copolymerization Methods 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
ANRQGKOBLBYXFM-UHFFFAOYSA-M phenylmagnesium bromide Chemical compound Br[Mg]C1=CC=CC=C1 ANRQGKOBLBYXFM-UHFFFAOYSA-M 0.000 description 3
-1 polyol compound Chemical class 0.000 description 3
238000010926 purge Methods 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
PWXIKGAMKWRXHD-UHFFFAOYSA-N 3-butylaziridin-2-one Chemical compound CCCCC1NC1=O PWXIKGAMKWRXHD-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
229920001400 block copolymer Polymers 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229910001623 magnesium bromide Inorganic materials 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
229920005862 polyol Polymers 0.000 description 2
UMLPONXXJIKBMA-UHFFFAOYSA-N 2-oxopyrrolidine-1-carbonyl chloride Chemical compound ClC(=O)N1CCCC1=O UMLPONXXJIKBMA-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
239000012190 activator Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000011952 anionic catalyst Substances 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000007033 dehydrochlorination reaction Methods 0.000 description 1
238000010612 desalination reaction Methods 0.000 description 1
YDVNLQGCLLPHAH-UHFFFAOYSA-N dichloromethane;hydrate Chemical compound O.ClCCl YDVNLQGCLLPHAH-UHFFFAOYSA-N 0.000 description 1
WOAZEKPXTXCPFZ-UHFFFAOYSA-N dimethyl(phenyl)azanium;chloride Chemical compound Cl.CN(C)C1=CC=CC=C1 WOAZEKPXTXCPFZ-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-IGMARMGPSA-N magnesium-24 Chemical compound [24Mg] FYYHWMGAXLPEAU-IGMARMGPSA-N 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
239000004753 textile Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1

Landscapes

Polyamides (AREA)

JP22018583A 1983-11-22 1983-11-22 ポリエ−テルポリアミドブロック共重合体の製造方法 Granted JPS60112825A (ja)

Priority Applications (5)

Application Number	Priority Date	Filing Date	Title
JP22018583A JPS60112825A (ja)	1983-11-22	1983-11-22	ポリエ−テルポリアミドブロック共重合体の製造方法
CA000467817A CA1257028A (fr)	1983-11-22	1984-11-14	Methode de preparation d'un copolymere a sequence de polyether-polyamide
DE8484308009T DE3485458D1 (de)	1983-11-22	1984-11-19	Herstellung von polyaether-polyamid-blockcopolymeren und prepolymeren.
EP84308009A EP0147051B1 (fr)	1983-11-22	1984-11-19	Préparation de copolymères polyether-polyamides et de leur prépolymères
US06/914,515 US4792603A (en)	1983-11-22	1986-10-02	Method of producing a polyether prepolymer

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP22018583A JPS60112825A (ja)	1983-11-22	1983-11-22	ポリエ−テルポリアミドブロック共重合体の製造方法

Publications (2)

Publication Number	Publication Date
JPS60112825A JPS60112825A (ja)	1985-06-19
JPS6363566B2 true JPS6363566B2 (fr)	1988-12-07

Family

ID=16747209

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP22018583A Granted JPS60112825A (ja)	1983-11-22	1983-11-22	ポリエ−テルポリアミドブロック共重合体の製造方法

Country Status (1)

Country	Link
JP (1)	JPS60112825A (fr)

1983
- 1983-11-22 JP JP22018583A patent/JPS60112825A/ja active Granted

Also Published As

Publication number	Publication date
JPS60112825A (ja)	1985-06-19

Publication	Publication Date	Title
US4031164A (en)	1977-06-21	Lactam-polyol-polyacyl lactam terpolymers
US3862262A (en)	1975-01-21	Lactam-polyol-acyl polyactam terpolymers
CA1061933A (fr)	1979-09-04	Polymerisation a catalyse anionique d'un lactame, amorcee par un polyester
US4034015A (en)	1977-07-05	Ester terminated terpolymers
US3993709A (en)	1976-11-23	Polyester initiated anionic catalyzed polymerization of lactam
EP0067695B1 (fr)	1986-10-15	Procédé de production de polymères séquencés à base de nylon
US4650608A (en)	1987-03-17	Star block copolymer from lactam and polyol and process for the production thereof
KR880002312B1 (ko)	1988-10-22	가교상으로 결합된 나일론 블록 공중합체 및 그의 제조방법
EP0161549A1 (fr)	1985-11-21	Matériaux portant une fonction halogénure d'acide
CA1232989A (fr)	1988-02-16	Solutions viscosifiees initiant la polymerisation du lactame
US5200498A (en)	1993-04-06	Lactam-lactone copolymer
JPS6363566B2 (fr)	1988-12-07
US4487920A (en)	1984-12-11	Polyamide-polyol-triazine block copolymer and anionic polymerization process
EP0147792B1 (fr)	1988-05-18	Procédé de condensation d'imide et d'alcool
KR880002239B1 (ko)	1988-10-20	N-치환된 아실-락탐 화합물을 제조하는 방법
JPS6132334B2 (fr)	1986-07-26
KR900004793B1 (ko)	1990-07-05	나일론-6-블록공중합체의 제조방법
JPH0119810B2 (fr)	1989-04-13
EP0194362B1 (fr)	1990-11-28	Procédé de préparation de composés acyl-lactame
CA1246266A (fr)	1988-12-06	Copolymeres a sequences en etoile; methode de preparation
EP0147051B1 (fr)	1992-01-15	Préparation de copolymères polyether-polyamides et de leur prépolymères
JPS614729A (ja)	1986-01-10	ポリエステルポリアミドブロツク共重合体及びその製造法
EP0241100A1 (fr)	1987-10-14	Compositions de copolymères-bloc de nylon à haute résistance aux chocs
EP0238131A2 (fr)	1987-09-23	Initiateur de polymérisation de lactame
JPH0136847B2 (fr)	1989-08-02