KR870008920A - 계면 활성 폴리카보디이미드 및 그의 분산액 - Google Patents
계면 활성 폴리카보디이미드 및 그의 분산액 Download PDFInfo
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- KR870008920A KR870008920A KR870003149A KR870003149A KR870008920A KR 870008920 A KR870008920 A KR 870008920A KR 870003149 A KR870003149 A KR 870003149A KR 870003149 A KR870003149 A KR 870003149A KR 870008920 A KR870008920 A KR 870008920A
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- polycarbodiimide
- residue
- surfactant
- carbodiimide
- alkylene oxide
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- 239000004094 surface-active agent Substances 0.000 title claims 13
- 239000006185 dispersion Substances 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 150000001718 carbodiimides Chemical class 0.000 claims description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims 9
- 239000000839 emulsion Substances 0.000 claims 7
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 claims 6
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 4
- -1 alkyl sulfides Chemical class 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 125000000524 functional group Chemical group 0.000 claims 4
- 230000002209 hydrophobic effect Effects 0.000 claims 4
- 150000002894 organic compounds Chemical class 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000004104 aryloxy group Chemical group 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims 2
- ZVBWPVOCTORPLM-UHFFFAOYSA-N formylsilicon Chemical compound [Si]C=O ZVBWPVOCTORPLM-UHFFFAOYSA-N 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 150000004756 silanes Chemical group 0.000 claims 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 2
- MFVFDTCSVFBOTL-UHFFFAOYSA-N 1,3-diazetidine Chemical group C1NCN1 MFVFDTCSVFBOTL-UHFFFAOYSA-N 0.000 claims 1
- 150000007945 N-acyl ureas Chemical class 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- YRTMEEURRDTMST-UHFFFAOYSA-N diazetidine Chemical group C1CNN1 YRTMEEURRDTMST-UHFFFAOYSA-N 0.000 claims 1
- KQNKVCOZMFJJGV-UHFFFAOYSA-N diazetidine-3-thione Chemical compound S=C1CNN1 KQNKVCOZMFJJGV-UHFFFAOYSA-N 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 본 발명의 카보디이미드를 제조하는 반응과정을 나타내는 반응도식이다.
Claims (22)
- 하기 일반식의 계면 활성 폴리카보디이미드.R-X-R′상기 식에서,R은 2개 이상의 카보디이미드 그룹을 함유하는 소수성 유기 화합물의 잔기이고 ;R'는 친구성 부분 및 카보디이미드 그룹과 반응할 수 있는 하나 이상의 작용성 그룹을 갖는 유기화합물의 잔기이며;X는 상기 카보디이미드 그룹과 상기 작용성 그룹과의 반응에 의해 형성되는 그룹이다.
- 제1항에 있어서, X가 우레티딘은, 디아제티딘 티은, N-아실 우레아, 구아니딘, 이소우레아, 이소티오우레아 및 카보디이미드로 이루어진 그룹중에서 선택된 게면 활성 폴리카보디이미드.
- 제1항에 있어서, R′가 하이드록실-함유 폴리(알킬렌 옥사이드)-기본 게면활성제의 잔기인 계면활성 폴리카보디이미드.
- 제3항에 있어서, 폴리(알킬렌 옥사이드)-기본 계면활성제가 알콕시-말단화된 계면 활성 폴리카보디이미드.
- 제4항에 있어서, 폴리(알킬렌 옥사이드)-기본 계면활성제가 메톡 시폴리에틸렌 글리콜인 계면 활성 폴리카보디이미드.
- 제4항에 있어서, 알킬렌 옥사이드 반복 단위의 수(n)가 약 15 내지 약 120인 계면 활성 폴리카보디이미드.
- 제1항에 있어서, R이 단일 분산 측쇄 폴리카보디이미드의 잔기인 계면 활성 폴리카보디이미드.
- 제7항에 있어서, 단일 분산 측쇄 폴리카보디이미드가 하기 일반식을 갖는 계면 활성 폴리카보디이미드.M-[(R″dN(N-R)n]-m-[(R″dN(N-R′)p-Q]q상기 식에서,M 및Q는 동일하거나 상이할 수 있으며, 각기 측쇄를 형성시키기 위한 부위로서, 작용하는 화합물의 잔기를 나타내고 ;R 및 R′는 동일하거나 상이할 수 있으며, 알킬(사이클로알킬 포함) 또는 아릴 ;시아노, 니트로, 할로, 알킬 설피이드, 디알-킬아미노알킬, 치환된 실란, 알콕시 및 아릴옥시 잔기일 수 있거나 이들을 함유하는 라디칼 또는 디라디칼 및 기타 치환된 상기 그룹들이고 ;R″는 시아노, 니트로, 할로, 알킬설차이드, 이알킬아미조, 치환된 실란, 알콕시 및 아릴옥시 잔기를 함유할 수 있는 동일하거나 상이한 알킬(사이클로알킬 포함) 또는 아릴 디라디칼 및 기타 치환된 상기 그룹들이며 ;d는 0 내지 약 12이고;n는 0 내지 약 6이며;m은 3 내지 약 5이고;p는 1내지 약 6이며;q는 0 내지 약 4이다.
- 제8항에 있어서, 단일분산 측쇄 폴리카보디이미드가 하기 일반식을 갖는 계면 활성 폴리카보디이미드.상기 식에서,R1,R2,R3, 및 R4는 동일하거나 상이할 수 있으며, 다직용성 카보디이미드를 의도된 목적으로 거의 방해 하지 않는 유기 잔기를 나타내고 ;D는 유기 잔기이며 ;r, s, t, x 및 y는 1 내지 약 6이다.
- 제8항에 있어서, 단일분산 측쇄 폴리카보디이미드가 하기 일반식을 갖는 계면 활성 폴리카보디이미드.상기 식에서,R1,R2, 및 R4는 동일하거나 상이할 수 잇으며, 탄소수 1내진 약 12의 알킬 그룹이고;R5및 R6는 동일하거나 상이 할 수 있으며, 수소, 알킬(사이클로알킬 포함, 아릴, 아르알킬,알크아릴,헤테로사이클릭, 시아노, 니트로, 할로, 알킬 설파이드, 디알킬아미노알킬, 실랄,아콕시, 실랄, 알콕시 아릴옥시그룹 및 치화된 상기 그룹들이며;Z는 측쇄를 형성하기 위한 부위로서 작용하는 화합물의 잔기이고;a,b,및c는 0내지 약 12이다.
- 제8항에 있어서, 단일분산, 측쇄 폴리카보디이미드가 1,3,6-트리-(N-이소프로필-N′-메틸렌카보디이미드)헥산인 계면 활성 폴리카보디이미드.
- 제8항에 있어서, 단일분산, 측쇄 콜리카보디이미드가 1,3,6-트리-(N-사이클로헥실-N′-메틸렌카보디이미드)헥산인 계면 활성 폴리 카보디이미드.
- 제8항에 있어서, 단일분산,측쇄 콜리카보디이미드가 1,3,6-트리-(N-n-부틸-N′-메틸렌카보디이미드)헥산인 계면 활성 폴리 카보디이미드.
- 제1항에 있어서, R이 다중분산, 선형 폴리카보디이미드의 잔기인 계면 활성 폴리카보디이미드.
- 제14항에 있어서, R이 모노-, 디- 및 트리-지환족 또는 포화 지방족 이소시아네이트 [여기에서 지환족 잔기는 5내지 약 7개의 탄소원자를 함유하며 탄소수 1낸지 약 6의 알킬, 또는 산소에 의해 치환 될 수 잇고, 포화 지방족 잔기는 1내지 약 18개의 탄소원자를 함유하며 모노-및트리이소시아네이트는임의적이다[의 반응으로부터 유도된 다가 PCDI의 잔기인 계면 활성 폴리카보디이미드.
- 수성 매질 중의 (a) 소수성 폴리카보디이미드 및 b) 일반식 R-X-R′ (여기에서, R은 적어도 2개의 카보디이미드 그룹을 함유하는 소수성 유기 화합물의 잔기이고, R′는 카보디이미드 그룹과 반응할 수 있는 작용성 그룹 적어도 하나와 소수성 부위를 갖는 유기 화합물의 잔기이며, X는 상기 카보디이미드 그룹과 상기 작용성 그룹과의 반응에 의해 형성된 그룹이다)의 계면 활성 폴리카보디임드의 혼합물을 함유하는 에멀젼
- 제16항에 있어서, X는가 우레티디논, 디아제티딘 티온, N- 아실우레아, 구아니딘, 이소우레아, 이소티오우레아, 및 카보디이미드로 이루어진 그룹중에서 선택된 에멀젼.
- 제16항에 있어서, R′가 하이드록실- 함유 폴리(알킬렌옥사이드)-기본 계면활성제인 에멀젼.
- 제18항에 있어서, 폴리(알킬렌 옥사이드)-기본 계면활성제가 알콕시에 의해 말단화된 에멀젼.
- 제19항에 있어서, 폴리(알킬렌 옥사이드)-기본 계면활성제가 메톡 시폴리에틸렌글리콜인 에멀젼.
- 제19항에 있어서, 알킬렌 옥사이드 반복단위의 수(n)가 약 15내지 약 120인 에멀젼.
- 제16항에 있어서, R이 단일분산, 측쇄 폴리카보디이미드인 에멀젼.※참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US845982 | 1986-03-31 | ||
US06/845,982 US4820863A (en) | 1986-03-31 | 1986-03-31 | Surface active polycarbodiimides |
Publications (1)
Publication Number | Publication Date |
---|---|
KR870008920A true KR870008920A (ko) | 1987-10-22 |
Family
ID=25296599
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR870003149A KR870008920A (ko) | 1986-03-31 | 1987-03-31 | 계면 활성 폴리카보디이미드 및 그의 분산액 |
Country Status (13)
Country | Link |
---|---|
US (3) | US4820863A (ko) |
EP (1) | EP0241805B1 (ko) |
JP (1) | JPS63264128A (ko) |
KR (1) | KR870008920A (ko) |
AT (1) | ATE59839T1 (ko) |
AU (1) | AU591764B2 (ko) |
BR (1) | BR8701461A (ko) |
DE (1) | DE3767199D1 (ko) |
DK (1) | DK162487A (ko) |
ES (1) | ES2020215B3 (ko) |
FI (1) | FI871414A (ko) |
NO (1) | NO871341L (ko) |
SG (1) | SG94891G (ko) |
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-
1986
- 1986-03-31 US US06/845,982 patent/US4820863A/en not_active Expired - Fee Related
-
1987
- 1987-03-31 ES ES87104762T patent/ES2020215B3/es not_active Expired - Lifetime
- 1987-03-31 NO NO871341A patent/NO871341L/no unknown
- 1987-03-31 KR KR870003149A patent/KR870008920A/ko not_active Application Discontinuation
- 1987-03-31 AU AU70796/87A patent/AU591764B2/en not_active Ceased
- 1987-03-31 FI FI871414A patent/FI871414A/fi not_active Application Discontinuation
- 1987-03-31 DE DE8787104762T patent/DE3767199D1/de not_active Expired - Lifetime
- 1987-03-31 BR BR8701461A patent/BR8701461A/pt unknown
- 1987-03-31 EP EP87104762A patent/EP0241805B1/en not_active Expired - Lifetime
- 1987-03-31 AT AT87104762T patent/ATE59839T1/de not_active IP Right Cessation
- 1987-03-31 DK DK162487A patent/DK162487A/da not_active IP Right Cessation
- 1987-04-21 JP JP62096380A patent/JPS63264128A/ja active Granted
-
1989
- 1989-01-30 US US07/303,231 patent/US5047588A/en not_active Expired - Fee Related
- 1989-03-13 US US07/322,492 patent/US5081173A/en not_active Expired - Fee Related
-
1991
- 1991-11-08 SG SG948/91A patent/SG94891G/en unknown
Also Published As
Publication number | Publication date |
---|---|
US4820863A (en) | 1989-04-11 |
AU591764B2 (en) | 1989-12-14 |
DK162487A (da) | 1987-10-01 |
FI871414A0 (fi) | 1987-03-31 |
SG94891G (en) | 1992-01-17 |
ATE59839T1 (de) | 1991-01-15 |
EP0241805A3 (en) | 1988-07-06 |
NO871341D0 (no) | 1987-03-31 |
EP0241805A2 (en) | 1987-10-21 |
US5081173A (en) | 1992-01-14 |
JPS63264128A (ja) | 1988-11-01 |
US5047588A (en) | 1991-09-10 |
EP0241805B1 (en) | 1991-01-09 |
DK162487D0 (da) | 1987-03-31 |
AU7079687A (en) | 1987-10-08 |
DE3767199D1 (de) | 1991-02-14 |
NO871341L (no) | 1987-10-01 |
ES2020215B3 (es) | 1991-08-01 |
BR8701461A (pt) | 1988-01-05 |
FI871414A (fi) | 1987-10-01 |
JPH0527450B2 (ko) | 1993-04-21 |
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