DE249225T1 - Verfahren zur herstellung eines pfropfcopolymers. - Google Patents
Verfahren zur herstellung eines pfropfcopolymers.Info
- Publication number
- DE249225T1 DE249225T1 DE198787108424T DE87108424T DE249225T1 DE 249225 T1 DE249225 T1 DE 249225T1 DE 198787108424 T DE198787108424 T DE 198787108424T DE 87108424 T DE87108424 T DE 87108424T DE 249225 T1 DE249225 T1 DE 249225T1
- Authority
- DE
- Germany
- Prior art keywords
- fluorine
- methacrylate
- copolymer
- acrylate
- process according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920000578 graft copolymer Polymers 0.000 title claims 2
- 238000004519 manufacturing process Methods 0.000 title 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 11
- 229910052731 fluorine Inorganic materials 0.000 claims 11
- 239000011737 fluorine Substances 0.000 claims 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 9
- 229920001577 copolymer Polymers 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- -1 isocyanate compound Chemical class 0.000 claims 7
- 239000011347 resin Substances 0.000 claims 5
- 229920005989 resin Polymers 0.000 claims 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 4
- 239000000178 monomer Substances 0.000 claims 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims 2
- 235000011187 glycerol Nutrition 0.000 claims 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 claims 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 claims 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 claims 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 claims 1
- 229910052770 Uranium Inorganic materials 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 claims 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 claims 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 claims 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
-
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/06—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyurethanes
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6275—Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds
- C08G18/6279—Polymers of halogen containing compounds having carbon-to-carbon double bonds; halogenated polymers of compounds having carbon-to-carbon double bonds containing fluorine atoms
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8108—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group
- C08G18/8116—Unsaturated isocyanates or isothiocyanates having only one isocyanate or isothiocyanate group esters of acrylic or alkylacrylic acid having only one isocyanate or isothiocyanate group
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/81—Unsaturated isocyanates or isothiocyanates
- C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
- C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
- C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/92—Polyurethane having terminal ethylenic unsaturation
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Paints Or Removers (AREA)
- Graft Or Block Polymers (AREA)
Claims (8)
1. Verfahren zur Herstellung eines Pfropfcopolymeren, dadurch gekenhz eichnet , daß man 99,5
bis 0,5 Gewichtsprozent eines ethylenisch ungesättigten Monomeren (B), das mit Doppelbindung des Harzes (A) copolymerisierbar
ist,in Anwesenheit von 0,5 bis 99,5 Gewichtsprozent eines fluorenthaltenden Harzes (A), welches
reaktive Doppelbindungen via eine Uranbindung in einer Menge von 0,001 bis 0f025 Mol pro 100 g des Harzes
(A) enthält polymerisiert.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet , daß das fluorenthaltende Harz (A)
durch Umsetzung eines fluorenthaltenden Copolymeren mit Hydroxylgruppen, einer mehrwertigen Isocyanatverbindung,
die zwei oder mehr Isocyanatgruppen enthält, und eines ethylenisch ungesättigten Monomeren, das eine Hydroxylgruppe
enthält, erhalten wird.
3. . Verfahren nach Anspruch 1, dadurch g e k e &eegr; &eegr; ze i c hn e t , daß das fluorenthaltende Harz (A)
durch Umsetzung eines fluorenthaltenden Copolymeren mit Hydroxylgruppen mit einem ethylenisch ungesättigten Monomeren,
das Isocyanatgruppen enthält, erhalten worden ist.
4. Verfahren nach Anspruch 2, dadurch gekennzeichnet , daß das fluorenthaltende Copolymere,
welches Hydroxylgruppen enthält, eine Hydroxylzahl von 0,57 bis 250 und einen Fluorgehalt von 1 bis 60 Gewichtsprozent
besitzt.
5. Verfahren nach Anspruch 4, dadurch gekennzeichnet, daß das fluorenthaltende Copolymere,
das Hydroxylgruppen enthält, ein Copolymeres ist, welches
als wesentliche Komponenten ein Fluorolefin, einen Hydroxyalkylvinylether
und einen Alkylvinylether oder einen Cycloalkylvinylether enthält.
6. Verfahren nach Anspruch 3, dadurch gekennzeichnet , daß das fluorenthaltende Copolymere,
das Hydroxylgruppen enthält, eine Hydroxylzahl von 0,57
bis 250 und einen Fluorgehalt von 1 bis 60 Gewichtsprozent aufweist.
7. Verfahren nach Anspruch 6, dadurch g e ken &eegr; zeichnet
, daß das fluorenthaltende Copolymere, das Hydroxylgruppen enthält, ein Copolymeres ist, das als
wesentliche Komponenten ein Fluorolefin, einen Hydroxyalkylvinylether
und einen Alkylvinylether oder einen Cycloalkylvinylether enthält.
8. Verfahren nach Anspruch 1, dadurch gekennzeichnet , daß das ethylenisch ungesättigte Monomere
mindestens eine Verbindung, ausgewählt aus der Gruppe Methylacrylat, Ethylacrylat, Butylacrylat, Isopropylacrylat,
2-Ethylhexylacrylat, Methylmethacrylat, Ethylmethacrylat,
Butylmethacrylat, Isopropylmethacrylat, 2-Ethylhexylmethacrylat, Styrol, Vinyltoluol, a-Methylstyrol,
Chlorstyrol, Acrylnitril, Methacrylnitril, Vinylchlorid, Vinylacetat, Dimethylmaleat, 2-Hydroxyethylacrylat,
2-Hydroxyethylmethacrylat, 2-Hydroxypropylacrylat,
2-Hydroxypropylmethacrylat, Monoacrylat von Glycerin, Monomethacrylat von Glycerin, Monoacrylat von
Trimethylolpropan, Monomethacrylat von Trimethylolpropan,
N-Methylolacrylamid and N-Methylolmethacrylamid, ist.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61138724A JPS62295914A (ja) | 1986-06-13 | 1986-06-13 | グラフト共重合体の製造法 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE249225T1 true DE249225T1 (de) | 1988-06-09 |
Family
ID=15228667
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE8787108424T Expired - Lifetime DE3768708D1 (de) | 1986-06-13 | 1987-06-11 | Verfahren zur herstellung eines pfropfcopolymers. |
DE198787108424T Pending DE249225T1 (de) | 1986-06-13 | 1987-06-11 | Verfahren zur herstellung eines pfropfcopolymers. |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE8787108424T Expired - Lifetime DE3768708D1 (de) | 1986-06-13 | 1987-06-11 | Verfahren zur herstellung eines pfropfcopolymers. |
Country Status (4)
Country | Link |
---|---|
US (2) | US4923929A (de) |
EP (1) | EP0249225B1 (de) |
JP (1) | JPS62295914A (de) |
DE (2) | DE3768708D1 (de) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5202394A (en) * | 1987-09-24 | 1993-04-13 | Hoechst Ag | Graft polymers with a polyurethane graft base, processes for their preparation and their use |
JPH01113451A (ja) * | 1987-10-27 | 1989-05-02 | Dainippon Toryo Co Ltd | 塗料用樹脂組成物 |
JPH02144179A (ja) * | 1988-11-22 | 1990-06-01 | Bou Kojima | 被塗装物へのポリテトラフルオロエチレン系塗料のコーティング方法 |
KR940003863B1 (ko) * | 1991-01-07 | 1994-05-04 | 한국과학기술연구원 | 혈액적합성이 개선된 불소화 폴리우레탄 |
JPH06113906A (ja) * | 1992-10-02 | 1994-04-26 | Maruzen Byora:Kk | くつ鋲の製造方法 |
DE69402993T2 (de) * | 1993-01-21 | 1997-10-23 | Akzo Nobel Nv | Wasserdispergierbares Hybridpolymer |
JP2882737B2 (ja) * | 1993-10-19 | 1999-04-12 | 昭和高分子株式会社 | 含フッ素重合体の製造方法 |
DE69435291D1 (de) * | 1993-10-28 | 2010-06-10 | Asahi Glass Co Ltd | Fluorid-enthaltender Polymerklebstoff und diesen gebrauchendes Laminat |
US5424364A (en) * | 1994-05-17 | 1995-06-13 | E. I. Du Pont De Nemours & Company | Comb pigment dispersants |
FR2733503B1 (fr) * | 1995-04-28 | 1997-07-18 | Gen Electric Plastics Abs Euro | Utilisation d'alliage polymere a base de polymerisat de tetrafluorethylene comme auxiliaire de traitement de certaines resines |
EP0812864A3 (de) * | 1996-06-11 | 1998-09-23 | Central Glass Company, Limited | Fluor enthaltendes Harz für einen Aufstrichstoff |
KR100466355B1 (ko) * | 1996-07-31 | 2005-06-16 | 미쯔비시 레이온 가부시끼가이샤 | 폴리테트라플루오로에틸렌함유혼합분체,이를함유하는열가소성수지조성물및그성형체 |
KR20120110143A (ko) * | 2009-12-28 | 2012-10-09 | 미쯔비시 레이온 가부시끼가이샤 | 방오 도료용 수지 분산체의 제조 방법 |
CN109485796B (zh) * | 2018-10-17 | 2021-04-23 | 沈阳化工大学 | 一种橡胶制品表面涂覆水溶性固化特氟龙材料及其制备方法 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE570822A (de) * | 1957-09-02 | |||
US3090664A (en) * | 1958-03-31 | 1963-05-21 | Du Pont | Graft polymerizing an unsaturated organic acid or salt thereof onto a nitrogen containing polymer substrate |
US3356628A (en) * | 1964-12-01 | 1967-12-05 | Minnesota Mining & Mfg | Copolymers of perfluoro acrylates and hydroxy alkyl acrylates |
US3488268A (en) * | 1965-12-02 | 1970-01-06 | Du Pont | Irradiation process for preparing graft copolymers |
US3632796A (en) * | 1969-02-11 | 1972-01-04 | Scm Corp | Saturated linear polymers having plural pendant ethylenic unsaturation |
US3607974A (en) * | 1969-02-11 | 1971-09-21 | Scm Corp | Thermosetting resin containing pendant unsaturation and monomer where monomer and pendency have identical functionality |
US3719638A (en) * | 1969-10-29 | 1973-03-06 | T Miranda | Radiation curable acrylic urethane monomers |
JPS4948190B1 (de) * | 1971-03-04 | 1974-12-19 | ||
DE2638666A1 (de) * | 1976-08-27 | 1978-03-02 | Volkswagenwerk Ag | Kraftstoff-einspritzeinrichtung |
US4233425A (en) * | 1978-11-15 | 1980-11-11 | The Dow Chemical Company | Addition polymerizable polyethers having pendant ethylenically unsaturated urethane groups |
CA1156795A (en) * | 1979-04-11 | 1983-11-08 | Richard G. Newell | Curable fluorocarbon substituted polyetherurethaneacrylates |
JPS59230020A (ja) * | 1983-06-14 | 1984-12-24 | Showa Highpolymer Co Ltd | 硬化可能な樹脂の製法 |
JPS59230019A (ja) * | 1983-06-14 | 1984-12-24 | Showa Highpolymer Co Ltd | 硬化可能な樹脂の製法 |
JPS60197719A (ja) * | 1984-03-19 | 1985-10-07 | Showa Highpolymer Co Ltd | 硬化可能な樹脂の製造方法 |
US4552932A (en) * | 1984-04-30 | 1985-11-12 | The B. F. Goodrich Company | Radiation curable polyurethanes |
US4572610A (en) * | 1984-05-21 | 1986-02-25 | Desoto, Inc. | Optical fiber buffer coated with halogenated dihydroxy-terminated polybutadienes |
JPS60245552A (ja) * | 1984-05-21 | 1985-12-05 | 日本カーバイド工業株式会社 | 紫外線遮蔽性樹脂フイルム |
JPH0635559B2 (ja) * | 1985-06-25 | 1994-05-11 | 旭硝子株式会社 | 塗料用組成物 |
-
1986
- 1986-06-13 JP JP61138724A patent/JPS62295914A/ja active Granted
-
1987
- 1987-06-11 DE DE8787108424T patent/DE3768708D1/de not_active Expired - Lifetime
- 1987-06-11 EP EP87108424A patent/EP0249225B1/de not_active Expired
- 1987-06-11 DE DE198787108424T patent/DE249225T1/de active Pending
- 1987-06-12 US US07/061,081 patent/US4923929A/en not_active Expired - Fee Related
-
1990
- 1990-02-27 US US07/485,513 patent/US5087675A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0249225A3 (en) | 1988-07-20 |
DE3768708D1 (de) | 1991-04-25 |
JPH0228607B2 (de) | 1990-06-25 |
EP0249225B1 (de) | 1991-03-20 |
EP0249225A2 (de) | 1987-12-16 |
US5087675A (en) | 1992-02-11 |
JPS62295914A (ja) | 1987-12-23 |
US4923929A (en) | 1990-05-08 |
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