NL8302928A - N-gesubstitueerde carbamoyl-lactam verbinding. - Google Patents

N-gesubstitueerde carbamoyl-lactam verbinding. Download PDF

Info

Publication number: NL8302928A
Authority: NL; Netherlands
Prior art keywords: lactam; caprolactam; compound; diisocyanate; nylon block
Prior art date: 1983-08-20

Application number

NL8302928A

Other languages

English (en)

Dutch (nl)

Original Assignee

Stamicarbon

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.)

1983-08-20

Filing date

1983-08-20

Publication date

1985-03-18

1983-08-20 Application filed by Stamicarbon filed Critical Stamicarbon

1983-08-20 Priority to NL8302928A priority Critical patent/NL8302928A/nl

1984-08-17 Priority to BR8404125A priority patent/BR8404125A/pt

1984-08-17 Priority to PL1984249231A priority patent/PL143375B1/pl

1984-08-17 Priority to US06/641,773 priority patent/US4540515A/en

1984-08-17 Priority to DE8484201192T priority patent/DE3468036D1/de

1984-08-17 Priority to CA000461249A priority patent/CA1221364A/fr

1984-08-17 Priority to EP84201192A priority patent/EP0134616B1/fr

1984-08-18 Priority to KR1019840004990A priority patent/KR860001552B1/ko

1984-08-20 Priority to JP59171688A priority patent/JPS6099128A/ja

1984-08-27 Priority to IN655/MAS/84A priority patent/IN162233B/en

1985-03-18 Publication of NL8302928A publication Critical patent/NL8302928A/nl

Links

229920005862 polyol Polymers 0.000 claims description 28
150000003077 polyols Chemical class 0.000 claims description 26
150000003951 lactams Chemical class 0.000 claims description 25
239000004677 Nylon Substances 0.000 claims description 23
229920001778 nylon Polymers 0.000 claims description 23
229920001400 block copolymer Polymers 0.000 claims description 21
150000001875 compounds Chemical class 0.000 claims description 16
239000004721 Polyphenylene oxide Substances 0.000 claims description 8
229920000570 polyether Polymers 0.000 claims description 8
238000000034 method Methods 0.000 claims description 6
238000012693 lactam polymerization Methods 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 2
239000002685 polymerization catalyst Substances 0.000 claims description 2
PQGAHNJECSVDEI-UHFFFAOYSA-N [CH2]CCCCC Chemical compound [CH2]CCCCC PQGAHNJECSVDEI-UHFFFAOYSA-N 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 50
-1 Lactam compounds Chemical class 0.000 description 15
239000003054 catalyst Substances 0.000 description 14
125000005442 diisocyanate group Chemical group 0.000 description 13
238000006243 chemical reaction Methods 0.000 description 11
229920001451 polypropylene glycol Polymers 0.000 description 7
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
229910052708 sodium Inorganic materials 0.000 description 6
239000011734 sodium Substances 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
239000000203 mixture Substances 0.000 description 5
239000005056 polyisocyanate Substances 0.000 description 5
229920001228 polyisocyanate Polymers 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
229920002359 Tetronic® Polymers 0.000 description 4
238000003776 cleavage reaction Methods 0.000 description 4
230000007017 scission Effects 0.000 description 4
241000282326 Felis catus Species 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
239000004952 Polyamide Substances 0.000 description 3
239000012190 activator Substances 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
150000002009 diols Chemical class 0.000 description 3
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
239000012948 isocyanate Substances 0.000 description 3
229920002647 polyamide Polymers 0.000 description 3
238000003756 stirring Methods 0.000 description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
KYIMHWNKQXQBDG-UHFFFAOYSA-N N=C=O.N=C=O.CCCCCC Chemical compound N=C=O.N=C=O.CCCCCC KYIMHWNKQXQBDG-UHFFFAOYSA-N 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
238000010539 anionic addition polymerization reaction Methods 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
229940091250 magnesium supplement Drugs 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
238000010107 reaction injection moulding Methods 0.000 description 2
239000012429 reaction media Substances 0.000 description 2
DVPHDWQFZRBFND-DMHDVGBCSA-N 1-o-[2-[(3ar,5r,6s,6ar)-2,2-dimethyl-6-prop-2-enoyloxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-[4-[(2s,3r)-1-butan-2-ylsulfanyl-2-(2-chlorophenyl)-4-oxoazetidin-3-yl]oxy-4-oxobutanoyl]oxyethyl] 4-o-[(2s,3r)-1-butan-2-ylsulfanyl-2-(2-chloropheny Chemical group C1([C@H]2[C@H](C(N2SC(C)CC)=O)OC(=O)CCC(=O)OC(COC(=O)CCC(=O)O[C@@H]2[C@@H](N(C2=O)SC(C)CC)C=2C(=CC=CC=2)Cl)[C@@H]2[C@@H]([C@H]3OC(C)(C)O[C@H]3O2)OC(=O)C=C)=CC=CC=C1Cl DVPHDWQFZRBFND-DMHDVGBCSA-N 0.000 description 1
CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
229930091371 Fructose Natural products 0.000 description 1
239000005715 Fructose Substances 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
DJOWTWWHMWQATC-KYHIUUMWSA-N Karpoxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1(O)C(C)(C)CC(O)CC1(C)O)C=CC=C(/C)C=CC2=C(C)CC(O)CC2(C)C DJOWTWWHMWQATC-KYHIUUMWSA-N 0.000 description 1
NPPQSCRMBWNHMW-UHFFFAOYSA-N Meprobamate Chemical compound NC(=O)OCC(C)(CCC)COC(N)=O NPPQSCRMBWNHMW-UHFFFAOYSA-N 0.000 description 1
229920002176 Pluracol® Polymers 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
NJHPWOQALXDSNZ-UHFFFAOYSA-N [Mg].[Br] Chemical compound [Mg].[Br] NJHPWOQALXDSNZ-UHFFFAOYSA-N 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
238000005266 casting Methods 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
239000008103 glucose Substances 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 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
239000004922 lacquer Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910001623 magnesium bromide Inorganic materials 0.000 description 1
229960004658 magnesium lactate Drugs 0.000 description 1
239000000626 magnesium lactate Substances 0.000 description 1
235000015229 magnesium lactate Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920005906 polyester polyol Polymers 0.000 description 1
239000000047 product Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000012783 reinforcing fiber Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
239000001540 sodium lactate Substances 0.000 description 1
229940005581 sodium lactate Drugs 0.000 description 1
235000011088 sodium lactate Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
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 1
150000004072 triols Chemical class 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
- C08G18/8074—Lactams
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
- C08G65/3332—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing carboxamide group
- C08G65/33327—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing carboxamide group cyclic
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
- C08G69/18—Anionic polymerisation
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
- C08G69/18—Anionic polymerisation
- C08G69/20—Anionic polymerisation characterised by the catalysts used
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/40—Polyamides containing oxygen in the form of ether groups

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)
Polyamides (AREA)

NL8302928A 1983-08-20 1983-08-20 N-gesubstitueerde carbamoyl-lactam verbinding. NL8302928A (nl)

Priority Applications (10)

Application Number	Priority Date	Filing Date	Title
NL8302928A NL8302928A (nl)	1983-08-20	1983-08-20	N-gesubstitueerde carbamoyl-lactam verbinding.
BR8404125A BR8404125A (pt)	1983-08-20	1984-08-17	Composto de carbamoil-lactama n-substituido,processo para a preparacao de um copolimero por blocos de nailon,e artigo
PL1984249231A PL143375B1 (en)	1983-08-20	1984-08-17	Method of obtaining nylon block copolymers
US06/641,773 US4540515A (en)	1983-08-20	1984-08-17	N-Substituted carbamoyl-lactam compound
DE8484201192T DE3468036D1 (de)	1983-08-20	1984-08-17	N-substituted carbamoyl-lactam compound
CA000461249A CA1221364A (fr)	1983-08-20	1984-08-17	Compose de carbamoyl-lactam n-substitue
EP84201192A EP0134616B1 (fr)	1983-08-20	1984-08-17	Composés carbamoyl lactame N-substitués
KR1019840004990A KR860001552B1 (ko)	1983-08-20	1984-08-18	나일론 블록 코폴리머의 제조방법
JP59171688A JPS6099128A (ja)	1983-08-20	1984-08-20	Ｎ−置換カルバモイル−ラクタム化合物、及びナイロンブロツクコポリマ−の製法
IN655/MAS/84A IN162233B (fr)	1983-08-20	1984-08-27

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8302928		1983-08-20
NL8302928A NL8302928A (nl)	1983-08-20	1983-08-20	N-gesubstitueerde carbamoyl-lactam verbinding.

Publications (1)

Publication Number	Publication Date
NL8302928A true NL8302928A (nl)	1985-03-18

Family

ID=19842287

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8302928A NL8302928A (nl)	1983-08-20	1983-08-20	N-gesubstitueerde carbamoyl-lactam verbinding.

Country Status (10)

Country	Link
US (1)	US4540515A (fr)
EP (1)	EP0134616B1 (fr)
JP (1)	JPS6099128A (fr)
KR (1)	KR860001552B1 (fr)
BR (1)	BR8404125A (fr)
CA (1)	CA1221364A (fr)
DE (1)	DE3468036D1 (fr)
IN (1)	IN162233B (fr)
NL (1)	NL8302928A (fr)
PL (1)	PL143375B1 (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL8400006A (nl) *	1984-01-03	1985-08-01	Stamicarbon	Werkwijze voor de condensatie van imide en alkohol.
JPS63291921A (ja) *	1987-05-22	1988-11-29	Sumitomo Chem Co Ltd	エチレン性不飽和基を有するポリエ−テルポリアミド共重合体
NL8801914A (nl) *	1988-07-30	1990-02-16	Stamicarbon	Omzettingsprodukten van met lactam geblokkeerde diisocyanaten en daarvan afgeleide polylactamblokcopolymeren.
NL8900001A (nl) *	1989-01-02	1990-08-01	Stamicarbon	Acyllactam functionele verbindingen en daarvan afgeleide polylactamblokcopolymeren.
NL8901570A (nl) *	1989-06-22	1991-01-16	Stamicarbon	N-gesubstitueerde carbamoyllactam functionele verbindingen en daarvan afgeleide polylactamblokcopolymeren.
BE1006897A3 (nl) *	1993-03-01	1995-01-17	Dsm Nv	Werkwijze voor het bereiden van een nylonblokcopolymeer.
KR20040015924A (ko) *	2002-08-14	2004-02-21	한명희	환경 및 건강 친화적 분필 조성물
ES2844323T3 (es) *	2010-03-01	2021-07-21	Lubrizol Advanced Mat Inc	Elastómeros de copolieteramida procesables en estado fundido
EP2520602A1 (fr) *	2011-05-03	2012-11-07	BrüggemannChemical L. Brüggemann KG	Composition pour la polymérisation anionique de lactame
WO2013012476A2 (fr) *	2011-07-21	2013-01-24	Arizona Chemical Company, Llc	Copolymères à blocs de polyéther-polyamide ramifiés et leurs procédés de fabrication et d'utilisation
EP2760906B1 (fr) *	2011-09-28	2017-03-01	Basf Se	Procédé de production de polyamides par polymérisation anionique
EP3253560B1 (fr)	2015-02-05	2019-11-06	Stratasys Ltd.	Impression en trois dimensions et commandée de façon numérique de matériaux polymérisables
JP7048502B2 (ja)	2016-02-05	2022-04-05	ストラタシスリミテッド	ポリアミド形成材料を使用する三次元インクジェット印刷
WO2018005731A1 (fr) *	2016-07-01	2018-01-04	Hercules Llc	Polymère fonctionnalisé par un lactame, compositions et applications de celui-ci
JP7476719B2 (ja) *	2020-08-13	2024-05-01	Ｕｂｅ株式会社	ポリアミドの製造方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL6904544A (fr) *	1969-03-25	1970-09-29
DE2707660C2 (de) *	1977-02-23	1985-12-19	Bayer Ag, 5090 Leverkusen	Abspalter- und Diolrest enthaltende Diisocyanat-Addukte, ihre Herstellung und Verwendung
DE2929224A1 (de) *	1979-07-19	1981-02-05	Huels Chemische Werke Ag	Herstellung von freie nco- und endstaendig mit epsilon -caprolactam blockierte nco-gruppen enthaltenden isophorondiisocyanataddukten, sowie danach hergestellte verbindungen
JPS5733014A (en) *	1980-08-05	1982-02-23	Nippon Denso Co Ltd	Cooler with cool box for vehicle

1983
- 1983-08-20 NL NL8302928A patent/NL8302928A/nl not_active Application Discontinuation
1984
- 1984-08-17 BR BR8404125A patent/BR8404125A/pt unknown
- 1984-08-17 EP EP84201192A patent/EP0134616B1/fr not_active Expired
- 1984-08-17 US US06/641,773 patent/US4540515A/en not_active Expired - Lifetime
- 1984-08-17 PL PL1984249231A patent/PL143375B1/pl unknown
- 1984-08-17 DE DE8484201192T patent/DE3468036D1/de not_active Expired
- 1984-08-17 CA CA000461249A patent/CA1221364A/fr not_active Expired
- 1984-08-18 KR KR1019840004990A patent/KR860001552B1/ko not_active Expired
- 1984-08-20 JP JP59171688A patent/JPS6099128A/ja active Pending
- 1984-08-27 IN IN655/MAS/84A patent/IN162233B/en unknown

Also Published As

Publication number	Publication date
US4540515A (en)	1985-09-10
CA1221364A (fr)	1987-05-05
EP0134616A1 (fr)	1985-03-20
EP0134616B1 (fr)	1987-12-09
PL249231A1 (en)	1985-06-04
KR860001552B1 (ko)	1986-10-04
IN162233B (fr)	1988-04-16
DE3468036D1 (de)	1988-01-21
JPS6099128A (ja)	1985-06-03
KR850001783A (ko)	1985-04-01
BR8404125A (pt)	1985-07-16
PL143375B1 (en)	1988-02-29

Legal Events

Date	Code	Title	Description
1985-03-18	A1B	A search report has been drawn up
1986-08-18	DNT	Communications of changes of names of applicants whose applications have been laid open to public inspection	Free format text: STAMICARBON B.V. TE GELEEN
1989-04-03	BV	The patent application has lapsed

Publication	Publication Date	Title
NL8302928A (nl)	1985-03-18	N-gesubstitueerde carbamoyl-lactam verbinding.
NL8400411A (nl)	1985-09-02	Werkwijze voor het bereiden van een nylonblokcopolymeercompositie.
EP0135233B1 (fr)	1988-02-17	Procédé de préparation de composé carbamoyl-lactame N-substitué
US5200498A (en)	1993-04-06	Lactam-lactone copolymer
NL8302929A (nl)	1985-03-18	Werkwijze voor het bereiden van een n-gesubstitueerde carbamoyl-lactam verbinding.
US4939234A (en)	1990-07-03	Polymerization of lactam polyisocyanate having the isocyanate groups blocked with lactam
EP0158393A1 (fr)	1985-10-16	Procédé de préparation d'un composé à base de carbamoyllactames N-substitués
US4843127A (en)	1989-06-27	Reactive elastomeric block co-oligomer and lactam-block copolymers derived therefrom
EP0320070B1 (fr)	1993-08-18	Procédé de préparation d'un copolymère en bloc de nylon
EP0194362B1 (fr)	1990-11-28	Procédé de préparation de composés acyl-lactame
BE1006638A3 (nl)	1994-11-03	Werkwijze voor het bereiden van een nylonblokcopolymeer.
KR880002239B1 (ko)	1988-10-20	N-치환된 아실-락탐 화합물을 제조하는 방법
CA1326729C (fr)	1994-02-01	Procede pour la production de polyamides modifies resistants a l'impact
KR910005341B1 (ko)	1991-07-25	락탐 공중합체의 제법
KR880002238B1 (ko)	1988-10-20	N-치환된 아실-락탐 화합물을 제조하는 방법
JPS59197428A (ja)	1984-11-09	変性ポリアミドの製造法
NL8303831A (nl)	1985-06-03	Werkwijze voor het bereiden van een n-gesubstitueerde carbamoyl-lactam verbinding.
JPS6325610B2 (fr)	1988-05-26
JPH0412292B2 (fr)	1992-03-04
JPS634855B2 (fr)	1988-02-01