KR910018433A - 가소성 수지, 그의 수성 분산액 및 그의 제조방법 - Google Patents
가소성 수지, 그의 수성 분산액 및 그의 제조방법 Download PDFInfo
- Publication number
- KR910018433A KR910018433A KR1019910005797A KR910005797A KR910018433A KR 910018433 A KR910018433 A KR 910018433A KR 1019910005797 A KR1019910005797 A KR 1019910005797A KR 910005797 A KR910005797 A KR 910005797A KR 910018433 A KR910018433 A KR 910018433A
- Authority
- KR
- South Korea
- Prior art keywords
- resin
- phenol
- polyoxyalkylenepolyamine
- polyepoxide
- reaction product
- Prior art date
Links
- 239000006185 dispersion Substances 0.000 title claims 2
- 239000000088 plastic resin Substances 0.000 title claims 2
- 238000002360 preparation method Methods 0.000 title 1
- 229920005989 resin Polymers 0.000 claims 10
- 239000011347 resin Substances 0.000 claims 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims 4
- 229920000647 polyepoxide Polymers 0.000 claims 4
- 239000007795 chemical reaction product Substances 0.000 claims 3
- -1 alkyl compound Chemical group 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 229920005862 polyol Polymers 0.000 claims 2
- 150000003077 polyols Chemical class 0.000 claims 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims 1
- 125000002091 cationic group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229930003836 cresol Natural products 0.000 claims 1
- 150000004985 diamines Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/34—Condensation polymers of aldehydes or ketones with monomers covered by at least two of the groups C08L61/04, C08L61/18 and C08L61/20
-
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/10—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
-
- 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
- C08G14/00—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
- C08G14/14—Block or graft polymers prepared by polycondensation of aldehydes or ketones on to macromolecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Epoxy Resins (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 폴리옥시알킬렌폴리아민, 포름알데히드 및 페놀의 반응 생성물로 이루어진 수지.
- 제1항에 있어서, 상기 반응의 반응물로서 폴리에폭시드를 더 포함하는 수지.
- 상기 항들중 어느 한 항에 있어서, 상기 폴리옥시알킬렌폴리아민이, X가 수소원자 또는 C1내지 C6의 알킬화합물을 나타내며, n이 1내지 50의 정수인 하기 일반식을 갖는 디아민을 포함하는 수지.
- 상기 항들중 어느 한 항에 있어서, 상기 폴리옥시알킬렌폴리아민이 X1,X2,X3가 각각 수소원자 또는 C1-C6의 알킬 화합물을 나타내며, a,b 및 c의 합이 3내지 30의 범위를 갖는 트리아민을 포함하는 수지.
- 상기 항들중 어느 한항에 있어서, 상기 페놀인 크레졸, 크실레놀, 레조르시놀, 나프톨 또는 페놀작용기를 갖는 올리고머 또는 비스페놀 A인 수지.
- 상기 항들중 어느 한항에 있어서, 평균 분자량수가 15,000 내지 40,000인 수지.
- 제2항 내지 제6항중 어느 한항에 있어서, 상기 폴리에폭시드가 폴리올의 폴리글리시딜 에테르인 수지.
- 제7항에 있어서, 상기 폴리올이 평군 분자량수가 약340 내지 2,000인 비스페놀 A의 폴리글리시딜 에테르를 포함하는 수지.
- 상기 항들중 어느 한항에 따른 반응생성물과 상기 반응생성물과는 다른 별도의 양이온 수지를 포함하는 가소성(可塑性)수지를 비휘발성 성분의 0.5 내지 30중량부로 포함하는 수성 분산액.
- 폴리에폭시드의 페놀 첨가생성물을 형성하기 위하여 폴리에폭시드를 페놀과 반응시킨 후, 포름알데히드 및 폴리옥시알킬렌폴리아민을 상기 첨가생성물과 반응시키는 단계를 포함하며, 전기코팅 조성물에 사용되기에 적합한 상기 제1항 내지 제8항중 어느 한항에 따른 수지 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7/507,927 | 1990-04-11 | ||
| US07/507.927 | 1990-04-11 | ||
| US07/507,927 US5298538A (en) | 1990-04-11 | 1990-04-11 | Plasticizing resins, aqueous dispersions thereof and methods of making the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR910018433A true KR910018433A (ko) | 1991-11-30 |
| KR100193313B1 KR100193313B1 (ko) | 1999-06-15 |
Family
ID=24020686
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019910005797A KR100193313B1 (ko) | 1990-04-11 | 1991-04-11 | 가소성 수지,그의 수성 분산액 및 제조방법 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5298538A (ko) |
| EP (1) | EP0451814B1 (ko) |
| JP (1) | JPH05214052A (ko) |
| KR (1) | KR100193313B1 (ko) |
| AU (1) | AU640216B2 (ko) |
| BR (1) | BR9101438A (ko) |
| CA (1) | CA2040147C (ko) |
| DE (1) | DE69110730T2 (ko) |
| ES (1) | ES2077706T3 (ko) |
| MX (1) | MX25286A (ko) |
| PH (1) | PH29903A (ko) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5789468A (en) * | 1997-03-27 | 1998-08-04 | E. I. Du Pont De Nemours And Company | Internal anticratering agent for cathodic electrocoating compositions |
| JP5053582B2 (ja) * | 2006-07-10 | 2012-10-17 | 積水化学工業株式会社 | 熱硬化性樹脂、及びそれを含む熱硬化性組成物、並びにそれから得られる成形体 |
| KR101406140B1 (ko) * | 2007-02-08 | 2014-06-19 | 주식회사 케이씨씨 | 폴리에폭사이드-폴리옥시알킬렌 아민 수지 및 그를포함하는 전착 도료 조성물 |
| JP5672440B2 (ja) * | 2010-09-30 | 2015-02-18 | ブラザー工業株式会社 | インクジェット記録用水性インク、インクジェット記録方法およびインクジェット記録装置 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4423166A (en) * | 1981-07-20 | 1983-12-27 | Ppg Industries, Inc. | Ungelled polyepoxide-polyoxyalkylenepolyamine resins, aqueous dispersions thereof, and their use in cationic electrodeposition |
| US4432850A (en) * | 1981-07-20 | 1984-02-21 | Ppg Industries, Inc. | Ungelled polyepoxide-polyoxyalkylenepolyamine resins, aqueous dispersions thereof, and their use in cationic electrodeposition |
| DE3380792D1 (en) * | 1982-07-26 | 1989-12-07 | Lowell O Cummings | Method for making phenol-formaldehyde-polyamine curing agents for epoxy resins |
| DE3329693A1 (de) * | 1983-08-17 | 1985-03-07 | Basf Farben + Fasern Ag, 2000 Hamburg | Verfahren zur herstellung von selbstvernetzenden kunstharzen und ihre verwendung |
| AT383819B (de) * | 1984-10-01 | 1987-08-25 | Vianova Kunstharz Ag | Verfahren zur herstellung kathodisch abscheidbarer elektrotauchlack-bindemittel |
| US4714750A (en) * | 1986-06-25 | 1987-12-22 | Texaco Inc. | Synthesis of products from polyoxyalkylene amines and 2,6-di-t-butylphenol for use as epoxy accelerators and curing agents |
-
1990
- 1990-04-11 US US07/507,927 patent/US5298538A/en not_active Expired - Lifetime
-
1991
- 1991-04-02 PH PH42238A patent/PH29903A/en unknown
- 1991-04-04 AU AU74085/91A patent/AU640216B2/en not_active Ceased
- 1991-04-10 EP EP91105684A patent/EP0451814B1/en not_active Expired - Lifetime
- 1991-04-10 MX MX2528691A patent/MX25286A/es unknown
- 1991-04-10 DE DE69110730T patent/DE69110730T2/de not_active Expired - Fee Related
- 1991-04-10 CA CA002040147A patent/CA2040147C/en not_active Expired - Lifetime
- 1991-04-10 BR BR919101438A patent/BR9101438A/pt not_active IP Right Cessation
- 1991-04-10 ES ES91105684T patent/ES2077706T3/es not_active Expired - Lifetime
- 1991-04-11 JP JP3106884A patent/JPH05214052A/ja active Pending
- 1991-04-11 KR KR1019910005797A patent/KR100193313B1/ko not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69110730T2 (de) | 1996-02-08 |
| BR9101438A (pt) | 1991-11-26 |
| KR100193313B1 (ko) | 1999-06-15 |
| AU7408591A (en) | 1991-10-17 |
| EP0451814A3 (en) | 1992-03-04 |
| DE69110730D1 (de) | 1995-08-03 |
| MX25286A (es) | 1993-12-01 |
| JPH05214052A (ja) | 1993-08-24 |
| ES2077706T3 (es) | 1995-12-01 |
| AU640216B2 (en) | 1993-08-19 |
| US5298538A (en) | 1994-03-29 |
| PH29903A (en) | 1996-09-16 |
| EP0451814A2 (en) | 1991-10-16 |
| CA2040147A1 (en) | 1991-10-12 |
| EP0451814B1 (en) | 1995-06-28 |
| CA2040147C (en) | 2003-12-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A201 | Request for examination | ||
| E902 | Notification of reason for refusal | ||
| E701 | Decision to grant or registration of patent right | ||
| GRNT | Written decision to grant | ||
| FPAY | Annual fee payment |
Payment date: 20110128 Year of fee payment: 13 |
|
| EXPY | Expiration of term |