GB766627A - Synthetic resinous compositions - Google Patents
Synthetic resinous compositionsInfo
- Publication number
- GB766627A GB766627A GB8190/55A GB819055A GB766627A GB 766627 A GB766627 A GB 766627A GB 8190/55 A GB8190/55 A GB 8190/55A GB 819055 A GB819055 A GB 819055A GB 766627 A GB766627 A GB 766627A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- weight
- polyvinyl
- replaced
- aldehyde
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of 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; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A resinous composition for coating fine wires consists essentially of (a) 40 to 99 per cent (by weight) of the reaction product of (1) 5 to 60 per cent (by weight) of an organosilicon compound of the general formula <FORM:0766627/IV(a)/1> , where each R is a monovalent hydrocarbon or halogenated hydrocarbon radical, each X is a halogen atom, alkoxy radical or hydroxy radical, n has an average value of from 1 to 2 and m has an average value of from 0.05 to 3; (2) 10 to 30 per cent by weight of a tri- or tetra-hydroxy alcohol; and (3) 30 to 70 per cent of a dicaboxylic acid, anhydride or lower alkyl ester; and (b) 1 to 60 per cent by weight of a polyvinyl acetal resin. If desired, up to 50 per cent by weight of (1) the organosilicon compound may be replaced with drying oils and/or drying oil acids, e.g. linseed, sardine, soyabean, dehydrated castor, tung, oiticica, perilla, chinawood, hempseed, poppyseed, safflower, sunflower-seed and walnut oils and the corresponding acids, (2) the polyhydric alcohol may be replaced by dihydric alcohols, e.g. ethylene and neopentyl glycols, and (3) the acetal resin may be replaced by a phenol-aldehyde resin obtained, e.g., from formaldehyde, acetaldehyde, benzaldehyde, cinnamic aldehyde or propionaldehyde and phenol, cresols, xylenols, wood oil phenols or petra-alkyl phenols. Essential components specified are:-organosilicon compounds-dimethyldichloro-, dibutyldiisopropoxy-, phenylmethyldiethoxy-, divinyldibutoxy-, tolyltriethoxy-, cyclohexyltrimethoxy-, phenylmethyldibromo-, (trifluoromethylphenyl) methyldichloro-, chlorophenyltriethoxy-,bromoxenyltrichloro-, stearylmethyldiethoxy- and allylstearyloxydimethoxy-silanes, mixtures and partial and/or complete hydrolysates thereof, diphenyl-, phenylmethyl-, dimethyl-, chlorophenylmethyl- and octadecylmethyl-silanediols and mixtures thereof; polyhydric alcohols-glycerine, pentaerythritol, trimethylol ethane and trimethylol propane; dicarboxylic acids-malonic, adipic, sebacic, maleic, dimethylmaleic, cyclohexyldicarboxylic, methylene disalicylic, phthalic, terephthalic, isophthalic, naphthalic, stilbenedicarboxylic, diphenic, tolane dicarboxylic and dibenzyl dicarboxylic acids; polyvinyl acetal resins-the condensation products of a polyvinyl ester, e.g. polyvinyl acetate, propionate or butyrate, and/or polyvinyl alcohol with an aldehyde, e.g. formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde and benzaldehyde. Examples are given. Specifications 691,013, 691,014, 691,015 and 715,231 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US766627XA | 1954-05-24 | 1954-05-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB766627A true GB766627A (en) | 1957-01-23 |
Family
ID=22133451
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8190/55A Expired GB766627A (en) | 1954-05-24 | 1955-03-21 | Synthetic resinous compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB766627A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0523242A1 (en) * | 1991-02-04 | 1993-01-20 | Kansai Paint Co. Ltd. | Curable resin composition |
WO2003093380A1 (en) * | 2002-04-30 | 2003-11-13 | Rotomac Electricals Pvt. Ltd | Self-priming chromate free corrosion resistant coating composition and method |
-
1955
- 1955-03-21 GB GB8190/55A patent/GB766627A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0523242A1 (en) * | 1991-02-04 | 1993-01-20 | Kansai Paint Co. Ltd. | Curable resin composition |
EP0523242A4 (en) * | 1991-02-04 | 1993-07-28 | Kansai Paint Co. Ltd. | Curable resin composition |
WO2003093380A1 (en) * | 2002-04-30 | 2003-11-13 | Rotomac Electricals Pvt. Ltd | Self-priming chromate free corrosion resistant coating composition and method |
US7208537B2 (en) | 2002-04-30 | 2007-04-24 | Rotomac Electricals Pvt, Ltd. | Self-priming chromate free corrosion resistant coating composition and method |
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