KR960007709A - 고광택 접착성 피복물 제조방법 및 이에 사용되는 라텍스 바인더 - Google Patents
고광택 접착성 피복물 제조방법 및 이에 사용되는 라텍스 바인더 Download PDFInfo
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- KR960007709A KR960007709A KR1019950025314A KR19950025314A KR960007709A KR 960007709 A KR960007709 A KR 960007709A KR 1019950025314 A KR1019950025314 A KR 1019950025314A KR 19950025314 A KR19950025314 A KR 19950025314A KR 960007709 A KR960007709 A KR 960007709A
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/062—Copolymers with monomers not covered by C09D133/06
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/44—Preparation of metal salts or ammonium salts
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Abstract
대기에 노출된 기질에 고광택 피복물을 생성하기에 적절한 라텍스 바인더 및 이와 같은 피복물 제조방법에 관한 것이다. 상기 바인더는 산작용성 부분과 암모니아 혹은 아민과 라텍스 중합체의 아세토아세틸 작용성펜던트 부분이 반응하여 형성된 엔아민 작용성 부분을 갖으며 분자량 및 산값이 낮은 라텍스 중합체를 포함한다. 라텍스 바인더를 함유하는 코팅제는 기질에 적용된 후 대기중의 빛과 공기에 노출되어 대기에 노출된 석회질 기질과 같이 접착되기 어려운 기질에 광택 및 접착성이 매우 우수한 피막을 형성한다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (9)
- 산작용성 펜던트 부분과 라텍스 중합체의 아세토아세틸 작용성 펜던트 부분이 암모니아 혹은 아민과 반응하여 형성된 엔아민 작용성 펜던트 부분을 갖으며 최대 분자량이 10,000-200,000이며 산값이 1-70인 라텍스 중합체가 분산되어 있고 수성 휘발성 캐리어를 포함하는 대기에 노출된 기질용 고광택 접착성 피복을 제조에 적절한 라텍스 바인더.
- 제1항에 있어서, 상기 중합체는 포스포에틸 메타크릴레이트, 아크릴산, 퓨마르산-모노에틸 에스테르, 퓨마르산, 이타콘산, 말레산, 말레산 무수물, 메타크릴산, 퓨마르산-모노에틸 에스테르, 메틸 하이드로젠 말레이트 및 이들의 결합으로 구성되는 그룹으로부터 선택된 산작용성 단량체를 상기 중합체 중량기준으로 0.2-10중량%로 사용하여 제조함을 특징으로 하는 라텍스 바인더.
- 제1항에 있어서, 상기 중합체는 하기 구조식을 갖는 아세토아세틸작용성 단량체를 중합체 2-20중량%로 제조됨을 특징으로 하는 라텍스 바인더.단, 상기 식에서, R1은 H, 1-10개의 탄소원자를 갖는 알킬 혹은 페닐이며; A는상기 식에서 R2는 H, 1-10개의 탄소원자를 갖는 알킬 혹은 페닐, 치환된 페닐, 할로, CO2CH3 혹은 CN; R3는 H, 1-10개의 탄소원자를 갖는 알킬 혹은 페닐, 치환된 페닐 혹은 할로; R4는 1-10개의 탄소원자를 갖는 알킬렌 혹은 페닐렌 혹은 치환된 페닐렌; R5는 알킬렌 혹은 치환된 알킬렌이며; a, m, n 및 q는 0 혹은 1이고; X 및 Y는 각각 -NH- 혹은 -O- ; B는 A, 1-10개의 탄소원자를 갖는 알킬 혹은 페닐, 치환된 페닐 혹은 헤토로고리(heterocyclic)이다.
- 제1항에 있어서, 상기 라텍스 중합체는 상기 산작용성 펜던트 부분을 갖는 제1중합체와 상기 아세토아세틸 작용성 펜던트 부분을 갖는 제2중합체를 포함함을 특징으로 하는 라텍스 바인더.
- 제4항에 있어서, 상기 라텍스 중합체는 나아가 상기 산작용성 펜던트 부분과 상기 아세토아세틸 작용성 펜던트 부분을 갖는 제3중합체를 포함함을 특징으로 하는 라텍스 바인더.
- 제1항에 있어서, 상기 라텍스 중합체의 평균 입자크기는 30-800nm임을 특징으로 하는 라텍스 바인더.
- pH가 8.5-9.5인 수성 휘발성 케리어; 최대분자량이 10,000-200,000이며 산값이 1-70이고 포스포에틸메타크릴레이트, 아크릴산, 퓨마르산-모노에틸 에스테르, 퓨마르산, 이타콘산, 말레산, 말레산 무수물, 메타그릴산, 퓨마르산-모노메틸 에스테르, 메틸 하이드로젠 말레이트 및 이들의 결합으로 구성되는 그룹으로부터 선택된 산작용성 단량체를 중합체의 중량을 기준으로 하여 중합체 0.2-10중량% 그리고 상기 중합체에 아세토아세틸 작용성 펜던트 부분을 부가하기 위해 아세토아세톡시에틸 메타크릴레이트, 아세토아세톡시 에틸 아크릴레이트, 아세토아세톡시프로필 메타크릴레이트, 아릴 아세토아세테이트, 아세토아세톡시부틸 메타크릴레이트, 2,3-디(아세토아세톡시)프로필 메타크릴레이트 혹은 이들의 결합으로 구성된 그룹으로부터 선택된 아세트아세틸 작용성 단량체를 중합체의 중량을 기준으로 하여 2-20중량%로 된 라텍스 중합체; 및 상기 아세토아세틸 작용성 펜던트 부분이 엔아민 작용성 펜던트 부분으로 유지되도록 첨가되는 안정한 양의 암모니아 혹은 아민;을 포함하는 대기에 노출된 기질용 고광택 접착성 피복물 제조에 적절한 라텍스 바인더.
- 산작용성 펜던트 부분과 라텍스 중합체의 아세토아세틸 작용성 펜던트 부분과 암모니아 혹은 아민이 반응하여 형성된 엔아민 작용성 펜던트 부분을 갖고 최대분자량은 10,000-200,000이며 산소값은 1-70인 라텍스 중합체가 분산되어 있고 pH가 8.5-9.5인 수성 휘발성 캐리어를 포함하는 라텍스 중합체 피막을 기질에 입히는 단계; 상기 피막에서 수성 휘발성 캐리어를 증발시키는 단계; 및 상기 피막을 화학광선과 공기에 노출시켜 상기 피막이 경화되어 상기 대기에 노출된 기질에서 고광택 접착성 피복물이 되도록 하는 단계;를 포함하는 대기에 노출된 기질용 고광택 접착성 피복물 제조방법.
- 제8항에 있어서, 상기 대기에 노출된 기질은 석회질 기질, 목재기질 혹은 시멘트 기질임을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29213094A | 1994-08-17 | 1994-08-17 | |
US08/292,130 | 1994-08-17 |
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Publication Number | Publication Date |
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KR960007709A true KR960007709A (ko) | 1996-03-22 |
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Application Number | Title | Priority Date | Filing Date |
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KR1019950025314A KR960007709A (ko) | 1994-08-17 | 1995-08-17 | 고광택 접착성 피복물 제조방법 및 이에 사용되는 라텍스 바인더 |
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US (1) | US5534310A (ko) |
EP (1) | EP0697417B1 (ko) |
JP (1) | JPH0881642A (ko) |
KR (1) | KR960007709A (ko) |
CN (1) | CN1116375C (ko) |
AU (1) | AU699161B2 (ko) |
BR (1) | BR9503663A (ko) |
CA (1) | CA2156348A1 (ko) |
DE (1) | DE69509712T2 (ko) |
ES (1) | ES2133676T3 (ko) |
ID (1) | ID23285A (ko) |
IL (1) | IL114801A0 (ko) |
TW (1) | TW416977B (ko) |
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WO2023213742A1 (en) * | 2022-05-06 | 2023-11-09 | Basf Se | Coating composition and preparation for the same |
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GB1185216A (en) * | 1966-05-28 | 1970-03-25 | Basf Ag | Production of coated, impregnated or bonded articles |
DE1644988B2 (de) * | 1967-06-28 | 1973-09-06 | Badische Anilin & Soda Fabrik AG, 6700 Ludwigshafen | Ueberzugs- und verklebungsmittel auf basis von gemischen von acetylacetatgruppen aufweisenden polymerisaten aethylenisch ungesaettigterverbindungen, acetoacetaten mehrwertiger metalle und verduennungsmittel |
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DE2535372C3 (de) * | 1975-08-08 | 1986-07-10 | Hoechst Ag, 6230 Frankfurt | Verfahren zum Herstellen von wäßrigen Kunststoff-Dispersionen |
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DE2927932A1 (de) * | 1979-07-11 | 1981-02-05 | Hoechst Ag | Vinylpolymer mit acetylacetoxygruppen, verfahren zu seiner herstellung und daraus erhaltenes mittel |
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AT384029B (de) * | 1986-04-30 | 1987-09-25 | Vianova Kunstharz Ag | 2-komponenten -acrylat-bindemittel |
US4908403A (en) * | 1986-05-02 | 1990-03-13 | Union Oil Of California | Pressure sensitive adhesives of acetoacetoxy-alkyl acrylate polymers |
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-
1995
- 1995-06-06 US US08/471,945 patent/US5534310A/en not_active Expired - Lifetime
- 1995-08-01 IL IL11480195A patent/IL114801A0/xx unknown
- 1995-08-04 EP EP95305472A patent/EP0697417B1/en not_active Expired - Lifetime
- 1995-08-04 ES ES95305472T patent/ES2133676T3/es not_active Expired - Lifetime
- 1995-08-04 DE DE69509712T patent/DE69509712T2/de not_active Expired - Lifetime
- 1995-08-07 AU AU28404/95A patent/AU699161B2/en not_active Expired
- 1995-08-10 ID IDP991003A patent/ID23285A/id unknown
- 1995-08-15 BR BR9503663A patent/BR9503663A/pt not_active IP Right Cessation
- 1995-08-16 CA CA002156348A patent/CA2156348A1/en not_active Abandoned
- 1995-08-17 KR KR1019950025314A patent/KR960007709A/ko not_active Application Discontinuation
- 1995-08-17 JP JP7230701A patent/JPH0881642A/ja not_active Withdrawn
- 1995-08-17 CN CN95115283A patent/CN1116375C/zh not_active Expired - Lifetime
- 1995-08-23 TW TW084108777A patent/TW416977B/zh not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP0697417B1 (en) | 1999-05-19 |
US5534310A (en) | 1996-07-09 |
TW416977B (en) | 2001-01-01 |
CN1116375C (zh) | 2003-07-30 |
ES2133676T3 (es) | 1999-09-16 |
DE69509712D1 (de) | 1999-06-24 |
AU2840495A (en) | 1996-02-29 |
DE69509712T2 (de) | 1999-11-11 |
BR9503663A (pt) | 1996-04-16 |
IL114801A0 (en) | 1995-12-08 |
AU699161B2 (en) | 1998-11-26 |
CN1123818A (zh) | 1996-06-05 |
CA2156348A1 (en) | 1996-02-18 |
ID23285A (id) | 1996-02-22 |
EP0697417A1 (en) | 1996-02-21 |
JPH0881642A (ja) | 1996-03-26 |
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