GB1305921A - - Google Patents
Info
- Publication number
- GB1305921A GB1305921A GB727070A GB727070A GB1305921A GB 1305921 A GB1305921 A GB 1305921A GB 727070 A GB727070 A GB 727070A GB 727070 A GB727070 A GB 727070A GB 1305921 A GB1305921 A GB 1305921A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mixture
- compound
- polyether
- reaction
- compounds
- 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.)
- Expired
Links
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
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
-
- 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
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/637—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers characterised by the in situ polymerisation of the compounds having carbon-to-carbon double bonds in a reaction mixture of saturated polymers and isocyanates
-
- 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/08—Polyurethanes from polyethers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
1305921 Synthetic resins DR BECK & CO AG 16 Feb 1970 [14 Feb 1969] 7270/70 Headings C3P and C3R Solvent free isooyanate reaction resins are prepared by reacting, in the absence of water, a polyether having an equivalent weight of 60 to 2000 and a functionality of 2 to 6, a thixotropic agent, a compound which accelerates the reaction between OH and NCO groups, a polyisocyanate, a homopolymerizable and/or copolymerizable monomeric compound having a b.p. of 120‹ to 200‹ C., a polymerization initiator and a polymerization accelerator for the monomeric compound. Fillers, pigments, compounds increasing the electrical conductivity of the resin, compounds to remove traces of water and fireproofing agents may be included in the reaction mixture. Suitably the polyether has an equivalent weight of 100 to 500 and a functionality of 3 or 4. The thixotropic agent is preferably a high-dispersal silicic acid. The homo- or copolymerizable monomer may be a vinyl aromatic compound, e.g. styrene, a vinyl ester, e.g. vinyl esters of C 9-11 acids with a methyl branch at the α-carbon atom, acrylic esters, e.g hydroxypropyl acrylate and allyl esters. Conventional polyisocyanates are used. Organic peroxides from the ketone-peroxide, per-acid and per-ester groups are the preferred compounds to initiate polymerization. In a typical example a mixture is formed from a highdispersal silicic acid, a branched polyether, red iron oxide, dolomite, a zeolite, dimethyl-aniline, styrene, dibutyltindilaurate and a compound to adjust the conductivity and this mixture is mixed with a mixture comprising a commercial diphenylmethane diisocyanate mixture and dibenzoyl peroxide. The resins produced are capable of being electrostatically sprayed to form coatings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT150669A AT300982B (en) | 1969-02-14 | 1969-02-14 | Electrostatically sprayable, solvent-free reaction paint |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1305921A true GB1305921A (en) | 1973-02-07 |
Family
ID=3515215
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB727070A Expired GB1305921A (en) | 1969-02-14 | 1970-02-16 |
Country Status (5)
Country | Link |
---|---|
AT (1) | AT300982B (en) |
BE (1) | BE745932A (en) |
DE (1) | DE2027114B2 (en) |
FR (1) | FR2035321A5 (en) |
GB (1) | GB1305921A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4289813A (en) | 1973-02-01 | 1981-09-15 | Bayer Aktiengesellschaft | Process for coating solvent-free lacquers |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4517222A (en) * | 1983-03-10 | 1985-05-14 | Ashland Oil, Inc. | Vaporous amine catalyst spray method of applying a film to a substrate |
-
1969
- 1969-02-14 AT AT150669A patent/AT300982B/en active
-
1970
- 1970-02-11 DE DE19702027114 patent/DE2027114B2/en not_active Withdrawn
- 1970-02-11 FR FR7004862A patent/FR2035321A5/fr not_active Expired
- 1970-02-13 BE BE745932D patent/BE745932A/en unknown
- 1970-02-16 GB GB727070A patent/GB1305921A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4289813A (en) | 1973-02-01 | 1981-09-15 | Bayer Aktiengesellschaft | Process for coating solvent-free lacquers |
Also Published As
Publication number | Publication date |
---|---|
DE2027114A1 (en) | 1970-12-10 |
DE2027114B2 (en) | 1978-05-11 |
AT300982B (en) | 1972-08-10 |
FR2035321A5 (en) | 1970-12-18 |
BE745932A (en) | 1970-07-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |