KR930700617A - Coating composition - Google Patents

Coating composition

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Publication number
KR930700617A
KR930700617A KR1019920702339A KR920702339A KR930700617A KR 930700617 A KR930700617 A KR 930700617A KR 1019920702339 A KR1019920702339 A KR 1019920702339A KR 920702339 A KR920702339 A KR 920702339A KR 930700617 A KR930700617 A KR 930700617A
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South Korea
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polydiorganosiloxane
composition
room temperature
group
carbon atoms
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KR1019920702339A
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Korean (ko)
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KR0175648B1 (en
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로드니 랠프 부룩스
미카넬 죤 윈터
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페터 보우간 대비이스
커어타울드스 코오팅스(홀딩스)리미티드
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Priority claimed from PCT/GB1991/000454 external-priority patent/WO1991014747A1/en
Publication of KR930700617A publication Critical patent/KR930700617A/en
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Publication of KR0175648B1 publication Critical patent/KR0175648B1/en

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Laminated Bodies (AREA)

Abstract

내용 없음.No content.

Description

피막 조성물Coating composition

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (31)

(A) (i) 일반식 (I)의 제1아민-관능성 실란(A) (i) the first amine-functional silane of formula (I) (RO)xR(3-x)SiR1NHR2(I)(RO) x R (3-x) SiR 1 NHR 2 (I) (식중 R은 동일하거나 다를 수 있는 기로서, 1-2개의 탄소원자를 갖고 있고 경우에 따라 에테르 결합을 포함 할 수 있는 1가 탄화수소기이고, R1은 2-4개의 탄소원자를 갖는 알킬렌기이거나 또는 3-8개의 탄소원자를 갖는 2가 지방족 에테르기이며, R2는 수소 또는 제1아미노 그룹으로 팁프 된 2-4개의 탄소원자를 갖는 알킬렌기이고, X는 2 또는 3의 정수이다)또는 ii) 일반식 (I)의 제1아민-관능성 실란과 일반식 (II)의 에폭시-관능성 실란의 반응 생성물Wherein R is a group which may be the same or different, and is a monovalent hydrocarbon group having 1-2 carbon atoms and, optionally, an ether bond, R 1 is an alkylene group having 2-4 carbon atoms, or Divalent aliphatic ether group having 3-8 carbon atoms, R 2 is hydrogen or an alkylene group having 2-4 carbon atoms tipped with a first amino group, X is an integer of 2 or 3) or ii) general Reaction product of the first amine-functional silane of formula (I) with the epoxy-functional silane of formula (II) A-Si(B)a(OB)(3-a)(II)A-Si (B) a (OB) (3-a) (II) (식중 A는 4-12개의 탄소원자를 갖는 에폭사이드-치환 1가 탄화수소이기고, B는 동일하거나 다를 수 있는 기로서 1-4개의 탄소원자를 갖는 알킬기이며, a는 0 또는 1의 정수이다), 또는 iii) 일반식 (I)의 제1아민-관능성 실란과 일반식 (III)의 알파, 오메가-디하이드록시폴리디메틸실록산 오일의 반응 생성물.(Wherein A is an epoxide-substituted monovalent hydrocarbon having 4-12 carbon atoms, B is an alkyl group having 1-4 carbon atoms as a group which may be the same or different, and a is an integer of 0 or 1), or iii) the reaction product of the first amine-functional silane of formula (I) and the alpha, omega-dihydroxypolydimethylsiloxane oil of formula (III). H O[Si (CH3)2O]yH (III)HO [Si (CH 3 ) 2 O] y H (III) (식중 y는 2 내지 60의 정수이다)중에서 선택된 아미노실란 물질, (B) 염화 폴리올레핀 및 (C) 실온 경화성 폴리디오르가노실록산으로 조정된 실온 가황성 실리콘 고무 피막의 접착력을 향상시키기 위하여 소지에 처리하는 프라이버 조성물.(Y is an integer from 2 to 60), the substrate is treated to improve the adhesion of the room temperature vulcanizable silicone rubber film adjusted with the aminosilane material selected from (B) chloride polyolefin and (C) room temperature curable polydiorganosiloxane. Privacy composition. 청구범위 1항에서, 실온 경화성 폴리디오르가노실록산(C)이 케티미 녹시실란 경화제와 함께 사용되는 알파,오메가-디하이드록시 폴리 디올가노실록산임을 특징으로 하는 조성물.The composition according to claim 1, wherein the room temperature curable polydiorganosiloxane (C) is an alpha, omega-dihydroxy polydiorganosiloxane used with a ketimioxysilane curing agent. 청구범위 1항에서, 실온 경화성 폴리디오르가노실록산(C)이 아실 옥시실란 경화제와 함께 사용되는 알파,오메가-디하이드록시 폴리 디올가노실록산임을 특징으로 하는 조성물.The composition of claim 1, wherein the room temperature curable polydiorganosiloxane (C) is an alpha, omega-dihydroxy polydiorganosiloxane used with an acyl oxysilane curing agent. 청구범위 1항에서, 실온 경화성 폴리디오르가노실록산(C)이 알콕시 실란 경화제와 함께 사용되는 알파,오메가-디하이드록시 폴리 디올가노실록산임을 특징으로 하는 조성물.The composition of claim 1 wherein the room temperature curable polydiorganosiloxane (C) is an alpha, omega-dihydroxy polydiorganosiloxane used with an alkoxy silane curing agent. 청구범위 1항에서, 실온 경화성 폴리디오르가노실록산(C)이 실리콘-결합 가수분해성 그룹으로 덮프 된 폴리디올가노실록산임을 특징으로 하는 조성물.The composition of claim 1 wherein the room temperature curable polydiorganosiloxane (C) is a polydiorganosiloxane covered with a silicon-bonded hydrolyzable group. 청구범위 5항에서, 실리콘-결합 가수분해성 케티미녹시, 아실옥시 또는 아민 그룹임을 특징으로 하는 조성물.7. A composition according to claim 5 which is a silicone-linked hydrolyzable ketiminoxy, acyloxy or amine group. 청구범위 1항 내지 6항중의 한 항에서, 염화 폴리올레핀이 17-40중량%의 염소함량을 갖고 있는 것임을 특징으로 하는 조성물.A composition according to claim 1, wherein the chlorinated polyolefin has a chlorine content of 17-40% by weight. 청구범위 1항 내지 7항중의 한 항에서, 조성물이 다른 염화 된 탄화수소 수지를 염화 폴리올레핀의 중량을 기준으로 1-100% 포함하고 있음을 특징으로 하는 조성물.8. A composition according to any one of claims 1 to 7, wherein the composition comprises 1-100% of the other chlorinated hydrocarbon resin by weight of the chlorinated polyolefin. 청구범위 1항 내지 8항중의 한 항에서, 아미노실란 물질(A)이 염화 폴리올레핀(B)과 조성물중에 존재하는 다른 염화 된 탄화수소 수지의 합계량을 기준으로 1-20%범위로 사용됨을 특징으로 하는 조성물.The method according to any one of claims 1 to 8, characterized in that the aminosilane material (A) is used in the range of 1-20% based on the total amount of the chlorinated polyolefin (B) and other chlorinated hydrocarbon resins present in the composition. Composition. 청구범위 1항 내지 9항중의 한 항에서, 염화 폴리올레핀(B)과 조성물중에 존재하는 다른 염화된 탄화수소수지의 합계량에 대한 실온 경화성 폴리디오르가노실록산(C)의 중량비가 1:1 내지 50:1임을 특징으로 하는 조성물.The weight ratio of room temperature curable polydiorganosiloxane (C) to the total amount of chlorinated polyolefin (B) and other chlorinated hydrocarbon resins present in the composition is from 1: 1 to 50: 1. A composition characterized in that. 청구범위 1항 내지 10항중의 한 항에서, 조성물이 안료를 포함하고 있음을 특징으로 하는 조성물.The composition of any one of claims 1 to 10, wherein the composition comprises a pigment. (A) (i) 일반식 (I)의 제1아민-관능성 실란(A) (i) the first amine-functional silane of formula (I) (RO)xR(3-x)SiR1NHR2(I)(RO) x R (3-x) SiR 1 NHR 2 (I) (식중 R은 동일하거나 다를 수 있는 기로서, 1-12개의 탄소원자를 갖고 있고 경우에 따라 에테르 결합을 포함 할 수 있는 1가 탄화수소기이고, R1은 2-4개의 탄소원자를 갖는 알킬렌기이거나 또는 3-8개의 탄소원자를 갖는 2가 지방족 에테르기이며, R2는 수소 또는 제1아미노 그룹으로 팁프 된 2-4개의 탄소원자를 갖는 알킬렌기이고, X는 2 또는 3의 정수이다)또는 ii) 일반식 (I)의 제1아민-관능성 실란과 일반식 (II)의 에폭시-관능성 실란의 반응 생성물Wherein R is a group which may be the same or different and is a monovalent hydrocarbon group having 1-12 carbon atoms and optionally comprising an ether bond, and R 1 is an alkylene group having 2-4 carbon atoms or Divalent aliphatic ether group having 3-8 carbon atoms, R 2 is hydrogen or an alkylene group having 2-4 carbon atoms tipped with a first amino group, X is an integer of 2 or 3) or ii) general Reaction product of the first amine-functional silane of formula (I) with the epoxy-functional silane of formula (II) A-Si(B)a(OB)(3-a)(II)A-Si (B) a (OB) (3-a) (II) (식중 A는 4-12개의 탄소원자를 갖는 에폭사이드-치환 1가 탄화수소이기고, B는 동일하거나 다를 수 있는 기로서 1-4개의 탄소원자를 갖는 알킬기이며, a는 0 또는 1의 정수이다), 또는 iii) 일반식 (I)의 제1아민-관능성 실란과 일반식 (III)의 알파, 오메가-디하이드록시폴리디메틸실록산 오일의 반응 생성물.(Wherein A is an epoxide-substituted monovalent hydrocarbon having 4-12 carbon atoms, B is an alkyl group having 1-4 carbon atoms as a group which may be the same or different, and a is an integer of 0 or 1), or iii) the reaction product of the first amine-functional silane of formula (I) and the alpha, omega-dihydroxypolydimethylsiloxane oil of formula (III). H O[Si (CH3)2O]yH (III)HO [Si (CH 3 ) 2 O] y H (III) (식중 y는 2 내지 60의 정수이다)중에서 선택된 아미노실란 물질, (B) 염화 폴리올레핀 및 (C) 실온 경화성 폴리디오르가노실록산과 혼합하여 프라이머 조성물을 제조하는 방법.A process for preparing a primer composition by mixing with an aminosilane material selected from (wherein y is an integer from 2 to 60), (B) chloride polyolefin and (C) room temperature curable polydiorganosiloxane. 청구범위 제12항에서, 착색 프라이머 조성물이 안료를 비반응성 폴리디오르가노실록산 오일에 분산 시킨 다음 아미노실란물질(A), 염화폴리올레핀(B) 및 실온 경화성 폴리디오르가노실록산(C)와 혼합하므로서 제조되고, 폴리디오르가노실록산 오일에 대한 안료 분산 공정이 안료가 아미노실록산 물질(A)또는 실온 경화성 디오르가노실록산(C)과 접촉하기전에 이루어짐을 특징으로 하는 방법.The method of claim 12 wherein the colored primer composition is prepared by dispersing the pigment in an unreactive polydiorganosiloxane oil and then mixing it with an aminosilane material (A), a chloride polyolefin (B) and a room temperature curable polydiorganosiloxane (C). And wherein the pigment dispersion process for the polydiorganosiloxane oil is carried out before the pigment is contacted with the aminosiloxane material (A) or room temperature curable diorganosiloxane (C). 청구범위 제12항에서, 착색 프라이머 조성물이 안료를 액상 하이드록실-덮프 폴리디오르가노실록산에 분산 시킨 다음 아미노실란물질(A), 염화폴리올레핀(B) 및 실온 경화성 폴리디오르가노실록산(C)와 혼합하는 공정에 의하여 제조되고, 액상 폴리디오르가노실록산 안료를 분산시키는 공정이 안료가 아미노실록산 물질(A)아 경화제 또는 실론 경화성 폴리디오르가노실록산(C)의 부분을 형성하는 실리콘-결합 가수분해서 그룹과 접촉하기 전에 이루어짐을 특징으로 하는 방법.The method of claim 12 wherein the colored primer composition disperses the pigment in a liquid hydroxyl-capped polydiorganosiloxane and then mixes it with an aminosilane material (A), a chloride polyolefin (B) and a room temperature curable polydiorganosiloxane (C). And a step of dispersing the liquid polydiorganosiloxane pigment, wherein the pigment forms a portion of an aminosiloxane material (A) curing agent or a Ceylon curable polydiorganosiloxane (C) hydrolyzed group and Before contacting. 청구범위 제12항에서, 착색 프라이머 조성물이 안료를 액상 하이드록실-덮프 폴리디오르가노실록산에 분산 시킨 다음 아미노실란물질(A), 염화폴리올레핀(B) 및 실온 경화성 폴리디오르가노실록산(C)을 형성하는 액상 하이드록실-덮프 폴리디오르가노실록산과 함께 있는 경화제와 혼합하는 공정으로 제조되고, 액상 하이드록실-팁프 폴리디오르가노실록산에 안료를 분산 시키는 공정이 안료가 아미노실록산 물질(A)나 경화제와 접촉하기 전에 이루어짐을 특징으로 하는 방법.The method of claim 12 wherein the colored primer composition disperses the pigment in a liquid hydroxyl-capped polydiorganosiloxane and then forms an aminosilane material (A), a chloride polyolefin (B) and a room temperature curable polydiorganosiloxane (C). It is prepared by mixing with a curing agent with a liquid hydroxyl-covered polydiorganosiloxane, and dispersing the pigment in the liquid hydroxyl-tipped polydiorganosiloxane, the pigment is in contact with the aminosiloxane material (A) or the curing agent Characterized in that before it is done. 소지를 청구범위 1항 내지 11항의 프라이머 조성물로 코팅하고 코팅된 프라이머 조성물 코팅층에 실온가황성 실리콘 고무 조성물을 처리함을 특징으로 하는 소지에 실온 가황성 실리콘 고무를 코팅하는 방법.A method of coating room temperature vulcanizable silicone rubber, characterized in that the base material is coated with the primer composition of claims 1 to 11 and the room temperature vulcanizable silicone rubber composition is treated to the coated primer composition coating layer. 청구범위 16항에서, 프라이머 조성물이 2하 내지 4항중의 한 항에 기재된 것이고 실온 가황성 실리콘 고무 조성물은 프라이머 조성물에서 사용된 것과 같은 형태의 경화제와 함께 사용되는 알파, 오메가-디하이드록시포리디오르가노실록산을 포함하고 있음을 특징으로 하는 방법.In Claim 16, the primer composition is as described in one of 2 to 4 below, and the room temperature vulcanizable silicone rubber composition is used in combination with a curing agent of the same type as used in the primer composition, alpha, omega-dihydroxyporidior A method comprising: organosiloxane. 청구범위 16항에서, 프라이머 조성물이 청구범위 5항 내지 6항에 기재된 것이고 실온 경화성 실리콘 고무 조성물은 실온 경화성 폴리디오르가노실록산(C)에서와 같은 형태의 실리콘-결합 가수분해성 그룹으로 팁프 된 폴리디오르가노실록산을 포함함을 특징으로 하는 법.In claim 16, the primer composition is as described in claims 5 to 6 and the room temperature curable silicone rubber composition is a polydior tipped with a silicone-bonded hydrolyzable group of the same type as in the room temperature curable polydiorganosiloxane (C). A method characterized by containing ganosiloxane. ※ 참고사항 : 최초출원 내용에 의하여 공개되는 것임.※ Note: This is to be disclosed by the original application.
KR1019920702339A 1990-03-27 1991-03-26 Coating composition KR0175648B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9006840.4 1990-03-27
GB909006840A GB9006840D0 (en) 1990-03-27 1990-03-27 Coating compositions
PCT/GB1991/000454 WO1991014747A1 (en) 1990-03-27 1991-03-26 Coating composition

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KR930700617A true KR930700617A (en) 1993-03-15
KR0175648B1 KR0175648B1 (en) 1999-05-01

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WO1998058007A1 (en) * 1997-06-17 1998-12-23 Konishi Co., Ltd. Process for the preparation of urethane resins and urethane resin compositions
US6165620A (en) * 1998-12-21 2000-12-26 General Electric Company Method of restoring damaged foul release coating area on a metallic surface, and surface obtained thereby
AU2004278075B2 (en) * 2003-10-03 2008-02-14 Hempel A/S A tie-coat composition comprising at least two types of functional polysiloxane compounds and a method for using the same for establishing a coating on a substrate
US20090042042A1 (en) * 2005-04-05 2009-02-12 Chugoku Marine Paints, Ltd. Tei Coat for Organopolysiloxane Antifouling Coat, Composite Coats, and Ships and Underwater Structures Covered with the Composite Coats
EP3778810A4 (en) * 2018-03-28 2021-12-22 Nitto Denko Corporation Undercoat layer-forming composition, undercoat layer, and coating film
WO2022202807A1 (en) * 2021-03-26 2022-09-29 日東電工株式会社 Layered body and primer composition

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FI101717B1 (en) 1998-08-14
FI924303A0 (en) 1992-09-25
NO923660L (en) 1992-09-21
NO303643B1 (en) 1998-08-10
PT97186B (en) 1998-07-31
GB9006840D0 (en) 1990-05-23
PT97186A (en) 1991-11-29
JP3205335B2 (en) 2001-09-04
FI101717B (en) 1998-08-14
NO923660D0 (en) 1992-09-21
CA2078144A1 (en) 1991-09-28
FI924303A (en) 1992-09-25
BR9106209A (en) 1993-03-23
KR0175648B1 (en) 1999-05-01
CA2078144C (en) 2002-07-30
JPH05505845A (en) 1993-08-26

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