KR910000586A - 스티렌 옥사이드 생성물 - Google Patents
스티렌 옥사이드 생성물 Download PDFInfo
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- KR910000586A KR910000586A KR1019890019208A KR890019208A KR910000586A KR 910000586 A KR910000586 A KR 910000586A KR 1019890019208 A KR1019890019208 A KR 1019890019208A KR 890019208 A KR890019208 A KR 890019208A KR 910000586 A KR910000586 A KR 910000586A
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Abstract
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Description
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Claims (18)
- 일반식(1) 또는 일반식(2)의 화합물, 이의 산에스테르 또는 이의 염.상기식에서 R은 탄소수 1 내지 24의 지방족 라디칼이고, "알킬렌"은 탄소수 2 또는 3의 알킬렌 라디칼이며, 치환체 쌍(Y1및 Y2) 및 (Y3및 Y4)중에서 한 개의 Y는 페닐이고 다른 한 개의 Y는 수소이며, m은 1내지 100의 수이다.
- 제1항에 있어서, 일반식(1) 및 (2)중에서 R이 탄소수 4내지 22의 알킬 또는 알케닐 라디칼인 화합물.
- 제1항에 있어서, 일반식(1) 및 (2)중에서 "알킬렌"이 에틸렌인 화합물.
- 제1항에 있어서, 일반식(1) 및 (2)중에서 m이 2내지 50인 화합물.
- 제1항에 있어서, 일반식(1) 및 (2)중에서 m이 2내지 25인 화합물.
- 제1항에 있어서, 하기 일반식(3)을 갖는 화합물.상기식에서, R1은 각각 탄소수 1내지 22의 알킬 또는 알케닐이고, Y1및 Y2중 하나는 페닐이며 다른 하나는 수소이고, m1은 2내지 40이다.
- 제1항에 있어서, 하기 일반식(4)를 갖는 산에스테르.상기식에서, R1은 각각 탄소수 1내지 22의 알킬 또는 알케닐이고, Y1및 Y2중 하나는 페닐이며 다른 하나는 수소이고, X는 말레산, 설포석신산, 황산 또는 인산 라디칼이며, m1은 2내지 40이다.
- 제1항에 있어서, 하기 일반식(5)를 갖는 산에스테르.상기식에서, R1은 각각 탄소수 1내지 22의 알킬 또는 알케닐이고, Y1및 Y2중 하나는 페닐이며 다른 하나는 수소이고,Z1및 Z2중 하나는 페닐이며 다른 하나는 수소이고, Z1및 Z2중 하나는 페닐이며 다른 하나는 수소이고, X는 말레산, 설포석신산, 황산 또는 인산 라디칼이며, n1과 n2의 합은 2내지 30이다.
- 제1항에 있어서, 하기 일반식(6)을 갖는 산에스테르.상기식에서, R1은 각각 탄소수 1내지 22의 알킬 또는 알케닐이고, Y1및 Y2중 하나는 페닐이며 다른 하나는 수소이고,Z1및 Z2중 하나는 메틸이며 다른 하나는 수소이고, X는 말레산, 설포석신산, 황산 또는 인산 라디칼이며, n1과 n2의 합은 2내지 30이다.
- 제1항에 있어서, 하기 일반식(7)을 갖는 화합물, 이의 산 에스테르 또는 이의 염.상기식에서, R1은 각각 탄소수 1내지 22의 알킬 또는 알케닐이고, "알킬렌"은 탄소수 2또는 3의 알킬렌 라디칼이며, Y1및 Y2중 하나는 페닐이며 다른 하나는 수소이며, m1은 2내지 40의 수이고, Y3및 Y4중 하나는 페닐이며 다른 하나는 수소이다.
- 제6항에 있어서, 일반식(3)중 식에서, R1이 3,5,5-트리메틸헥실이고, m1이 2인 화합물.
- 제6항에 있어서, 일반식(3)중 식에서, R1이 도데실이고, m1이 2인 화합물.
- 제7항에 있어서, 일반식(4)중 식에서, R1이 도데실이고, X가 말레산 라디칼이며, m1이 2인 화합물.
- 제7항에 있어서, 일반식(4)중 식에서, R1이 도데실이고, X가 황산 라디칼이며, m1이 2인 화합물.
- 제10항에 있어서, 일반식(7)중에서 식 R1이 3,5,5-트리메틸헥실이고, "알킬렌"이 에틸렌이며, m1은 10인 화합물
- 일반식(1) 또는 일반식(2)의 화합물의 산에스테르 2 내지 50중량%, 비이온성 계면활성제 5내지 50중량% 및 실리콘 60중량% 에틸렌성 불포화 지방족 디카복실산의 디알킬 에스테르 20내지 45중량%, 지방족 또는 방향족 카복실산 에스테르 또는 알킬벤젠 10내지 70중량%, C10내지 C24지방산과 다가 금속의 염 0.5 내지 5중량% 및 탄소수가 10내지 24인 지방산의 C1내지 C4알킬렌 다아미드 0.5내지 3중량%중 하나 이상을 함유함을 특징으로 하는 수성 또는 비-수성 제제(여기서, 각 함량은 수성 또는 비수성 제제의 총량을 기준으로 한 것이다.)상기식에서, R1은 각각 탄소수 1내지 24의 지방족 라디칼이고, "알킬렌"은 탄소수 2또는 3의 알킬렌 라디칼이며, Y1및 Y2중 하나는 페닐이며 다른 하나는 수소이며, m1은 2내지 100이고, Y3및 Y4중 하나는 페닐이며 다른 하나는 수소이다.
- 일반식(1) 또는 일반식(2)의 비이온성 스티렌옥사이드 생성물 15내지 50중량%, 일반식(7)의 화합물의 산 에스테르 또는 이의 염의 4급화 생성물 1내지 5중량%, 및 일반식(8)의 4급 암모늄 화합물 2내지 20중량%를 일반식(9)의 폴리알킬렌 글리콜 에테르 0.5내지 25중량% 및 일반식(10)의 질소-함유 비이온성 화합물 0.5내지 5중량%중에서 선택된 하나이상의 성분의 존재 또는 부재하에, 함유량을 특징으로 하는 수성제제(여기서, 각 함량은 수성제제의 총량을 기준으로 한 것이다.)상기식에서, R1은 각각 탄소수 1내지 24의 지방족 라디칼이고, "알킬렌"은 일반식(1) 및 (2)에서는 탄소수 2또는 3의 알킬렌 라디칼이며, 일반식(9)에서는 에틸렌 또는 프로필렌이고, 치환체 쌍 (Y1및 Y2) 및 (Y3및 Y4)중에서 한 개의 Y는 페닐이며 다른 한 개의 Y는 수소이고 , m은 1내지 100의 수이며, R1은 탄소수 12 내지 22의 알킬 또는 알케닐이고, Z′ 및 Z″중 하나는 수소, 메틸 또는 페닐이며 다른 하나는 수소이고, S1및 S2는 각각 S1과 S2의 합이 2내지 100이 되도록 하는 정수이며, R″는 탄소수 12내지 22의 알킬 또는 알케닐 라디칼이고, V1는 치환되거나 치환되지 않은 알킬이며,는 무기 또는 유기산의 음이온이고, P1및 P2는 각각 P1및 P2의 합이 2내지 100이 되도록 하는 정수이며, R″′은 탄소수 4내지 22의 알킬 또는 알케닐 라디칼이고, q는 2내지 85이며, Y′ 및 Y″중 하나는 페닐이며 다른 하나는 수소이고, x 및 y는 각각, x와 y의 합이 88내지 140이 되도록 하는 정수이다.
- 제1항에 따른 일반식(1) 또는 일반식(2)의 비이온성 스티렌 옥사이드 생성물 또는 이의 음이온성 산에스테르 또는 이의 염, 또는 비이온성 스티렌 옥사이드 부가물과 음이온성 스티렌 옥사이드 부가물의 혼합물의 존재하에서 처리함을 특징으로 하여, 적절한 염료의 존재 또는 부재하에 천연 또는 합성 섬유물질의 직물을 처리하는 방법.상기식에서, R은 탄소수 1내지24의 지방족 라디칼이고, "알킬렌"은 탄소수 2또는 3의 알킬렌 라디칼이며, 치환체 쌍 (Y1및 Y2) 및 (Y3및 Y4)중에서 한 개의 Y는 페닐이며 다른 한 개의 Y는 수소이고 , m은 1내지 100의 수이다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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Application Number | Priority Date | Filing Date | Title |
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CH2298/89-8 | 1989-06-20 | ||
CH229889 | 1989-06-20 |
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KR910000586A true KR910000586A (ko) | 1991-01-29 |
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KR1019890019208A KR910000586A (ko) | 1989-06-20 | 1989-12-22 | 스티렌 옥사이드 생성물 |
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EP (1) | EP0403718A3 (ko) |
JP (1) | JPH0662474B2 (ko) |
KR (1) | KR910000586A (ko) |
AU (1) | AU605055B1 (ko) |
CA (1) | CA2006424A1 (ko) |
DK (1) | DK660689A (ko) |
NZ (1) | NZ231926A (ko) |
ZA (1) | ZA899822B (ko) |
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ZA909267B (en) * | 1990-03-09 | 1991-09-25 | Ici Australia Operations | Fatty alcohol alkoxylate |
DE19940797A1 (de) * | 1999-08-27 | 2001-03-01 | Goldschmidt Ag Th | Durch Akoxylierung erhaltene blockcopolymere, styrenoxidhaltige Polyalkylenoxide und deren Verwendung |
DE10029648C1 (de) * | 2000-06-15 | 2002-02-07 | Goldschmidt Ag Th | Blockcopolymere Phosphorsäureester, deren Salze und deren Verwendung als Emulgatoren und Dispergiermittel |
DE10245099A1 (de) * | 2002-09-27 | 2004-04-08 | Goldschmidt Ag | Polyurethan-Verdickungsmittel zur Verdickung wässriger Systeme |
DE10252452B4 (de) | 2002-11-12 | 2006-07-06 | Clariant Gmbh | Styroloxidhaltige Copolymere und deren Verwendung als Emulgatoren und Dispergiermittel |
DE10348825A1 (de) * | 2003-10-21 | 2005-06-02 | Goldschmidt Ag | Dispergiermittel zur Herstellung wässriger Pigmentpasten |
DE102006002800A1 (de) * | 2006-01-20 | 2007-08-02 | Clariant International Limited | Dispergiermittel für wässrige Pigmentpräparationen |
US20100210461A1 (en) * | 2007-07-20 | 2010-08-19 | Basf Se | Compositions comprising alcohol alkoxylates, and use of the alcohol alkoxylates as adjuvant for the agrochemical sector |
JP5230338B2 (ja) * | 2008-10-07 | 2013-07-10 | 第一工業製薬株式会社 | ポリエステル繊維用均染剤 |
DE102012018544A1 (de) * | 2012-09-19 | 2014-03-20 | Clariant International Ltd. | Derivate der Sulfobernsteinsäure als Dispergiermittel in bindemittelfreien Pigmentpräparationen |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6144924A (ja) * | 1984-08-09 | 1986-03-04 | Dai Ichi Kogyo Seiyaku Co Ltd | 低活性ポリオキシアルキレン化合物の製造方法 |
JPS61204012A (ja) * | 1985-03-05 | 1986-09-10 | Miyoshi Oil & Fat Co Ltd | 消泡剤 |
US4713482A (en) * | 1985-03-26 | 1987-12-15 | Ciba-Geigy Corporation | Maleic or phthalic acid half esters of alkoxylated fatty amines |
WO1989012618A1 (en) * | 1988-06-20 | 1989-12-28 | Ppg Industries, Inc. | Polymerizable surfactant |
EP0378048A1 (de) * | 1988-12-23 | 1990-07-18 | Ciba-Geigy Ag | Styroloxid-Anlagerungsprodukte |
-
1989
- 1989-12-14 EP EP19890810958 patent/EP0403718A3/de not_active Withdrawn
- 1989-12-21 CA CA002006424A patent/CA2006424A1/en not_active Abandoned
- 1989-12-21 NZ NZ231926A patent/NZ231926A/en unknown
- 1989-12-21 ZA ZA899822A patent/ZA899822B/xx unknown
- 1989-12-22 JP JP1331424A patent/JPH0662474B2/ja not_active Expired - Lifetime
- 1989-12-22 DK DK660689A patent/DK660689A/da not_active Application Discontinuation
- 1989-12-22 AU AU47222/89A patent/AU605055B1/en not_active Ceased
- 1989-12-22 KR KR1019890019208A patent/KR910000586A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0403718A3 (de) | 1991-12-27 |
ZA899822B (en) | 1992-07-29 |
CA2006424A1 (en) | 1990-12-20 |
NZ231926A (en) | 1992-06-25 |
JPH0324029A (ja) | 1991-02-01 |
JPH0662474B2 (ja) | 1994-08-17 |
EP0403718A2 (de) | 1990-12-27 |
DK660689A (da) | 1990-12-21 |
DK660689D0 (da) | 1989-12-22 |
AU605055B1 (en) | 1991-01-03 |
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