GB588018A - Compositions comprising unsaturated polymeric materials and alkane dithiols - Google Patents
Compositions comprising unsaturated polymeric materials and alkane dithiolsInfo
- Publication number
- GB588018A GB588018A GB2031/45A GB203145A GB588018A GB 588018 A GB588018 A GB 588018A GB 2031/45 A GB2031/45 A GB 2031/45A GB 203145 A GB203145 A GB 203145A GB 588018 A GB588018 A GB 588018A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dithiol
- compositions
- butadiene
- unsaturated
- polymers
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
Abstract
Compositions comprise an organic solvent soluble polymeric organic material having a plurality of ethylenic linkages but otherwise free of groups which are reactive with the thiol group (see Group IV) and a monomeric alkane dithiol. The invention also includes the insolubilisation of the composition by exposure to an oxygen-containing atmosphere. Included in the unsaturated polymeric materials are partially polymerised drying oils, e.g., heat-bodied linseed and chinawood oils. A drier used in the varnish art, e.g., iron linoleate or resinate, may be added. The compositions may be compounded with pigments, fillers, synthetic resins, gums, cellulose derivatives and waxes and used for coatings, moulding compositions, adhesives and for printing ink ingredients.ALSO:Compositions comprise an organic solvent-soluble polymeric organic material having a plurality of ethylenic linkages but otherwise free of groups which are reactive with the thiol group and a monomeric alkane dithiol. The invention also includes the insolubilisation of the composition by exposure to an oxygen-containing atmosphere. A drier used in the varnish art, e.g. iron linoleate or resinate, may be added to the composition. Polymeric poly-unsaturated materials specified are polymers of allene, vinylcyclohexene, cyclopentadiene, 1.2-bis(vinyloxy)ethane, divinylformal, divinyl acetal and divinyl sulphide, the reaction products of polyhydric alcohols with polycarboxylic acids, polyethers, polysulphides, polyamide-polyesters and polyacetals prepared from components at least one of which contains an olefinic bond, heat-bodied linseed and chinawood oil, polymers of butadiene-1.3, isoprene and dimethyl-2.3-butadiene-1.3 and copolymers of the latter with styrene, pinene, isobutylene, camphene, monovinyl acetylene, vinyl ethinyl alkyl carbinols, vinyl acetate and chloride, acrolein, methyl vinyl ketone, acrylic and methacrylic acids and their esters, amides, imides and nitriles, alpha-chloro-acrylic acid and its esters, furylacrylic acid and its esters and dimethyl fumarate. Naturally occurring unsaturated polymers, e.g. natural rubber and gutta percha may also be used. Suitable alkane dithiols are 1.2-ethane dithiol, 1.3-propane dithiol, 1.8-octane dithiol, 1.6-octane dithiol and 1.10-octadecane dithiol. The compositions may be compounded with pigments, fillers, synthetic resins, gums, cellulose derivatives and waxes and used for coatings, moulding compositions, adhesives and for printing ink ingredients. In examples, cellulose acetate methacrylate (preparation described) and 2-ethyl-hexane-dithiol-1.3 are insolubilized by heating 1.10-decane dithiol is used to insolubilize ethylene glycol maleate resin, a resinous mixed glyceride of coconut oil acids and maleic acid, a resinous mixed glyceride of phthalic anhydride and methacrylic acid and a copolymer of butadiene and methyl methacrylate; and ethane dithiol to insolubilize butadiene-styrene and butadiene-acrylonitrile copolymers, natural rubber and polyfluoroprene.ALSO:Compositions comprise an organic solvent soluble polymeric organic material having a plurality of ethylenic linkages but otherwise free of groups which are reactive with the thiol group (see Group IV) and a monomeric alkane dithiol. The invention adso includes the insolubilization of the composition by exposure to an oxygen-containing atmosphere. Included in the unsaturated polymeric materials are natural rubber, gutta percha, and synthetic rubbers, e.g., polymers of butadiene 1.3 isoprene and dimethyl-2.3-butadiene-1.3 and copolymers thereof with other unsaturated organic compounds. A drier used in the varnish art, e.g., iron linoleate or resinate, may be added. The compositions may be compounded with pigments, fillers, synthetic resins, gums, cellulose derivatives and waxes and used for coatings, moulding compositions, adhesives and for printing ink ingredients.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US588018XA | 1944-01-25 | 1944-01-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB588018A true GB588018A (en) | 1947-05-12 |
Family
ID=22019012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2031/45A Expired GB588018A (en) | 1944-01-25 | 1945-01-25 | Compositions comprising unsaturated polymeric materials and alkane dithiols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB588018A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2166749A (en) * | 1984-11-05 | 1986-05-14 | Ici Plc | Coating compositions |
US7288608B2 (en) * | 2001-10-10 | 2007-10-30 | Regents Of The University Of Colorado | Degradable thiol-ene polymers |
CN102888149A (en) * | 2011-07-20 | 2013-01-23 | 上海申悦油墨有限公司 | Novel NK white gravure ink |
CN102888148A (en) * | 2011-07-20 | 2013-01-23 | 上海申悦油墨有限公司 | Novel HS white gravure ink |
US9988433B2 (en) | 2013-03-14 | 2018-06-05 | Mosaic Biosciences, Inc. | Covalent modification of biological macromolecules |
US9987393B2 (en) | 2011-01-28 | 2018-06-05 | The Regents Of The University Of Colorado, A Body | Covalently cross linked hydrogels and methods of making and using same |
US10016505B2 (en) | 2012-02-02 | 2018-07-10 | Mosaic Biosciences, Inc. | Biomaterials for delivery of blood extracts and methods of using same |
US10912837B2 (en) | 2015-02-09 | 2021-02-09 | Mosaic Biosciences, Inc. | Degradable thiol-ene polymers and methods of making thereof |
-
1945
- 1945-01-25 GB GB2031/45A patent/GB588018A/en not_active Expired
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2166749A (en) * | 1984-11-05 | 1986-05-14 | Ici Plc | Coating compositions |
US4730033A (en) * | 1984-11-05 | 1988-03-08 | Imperial Chemical Industries Plc | Coating compositions |
AU581468B2 (en) * | 1984-11-05 | 1989-02-23 | Imperial Chemical Industries Plc | Coating compositions |
US10189952B2 (en) | 2001-10-10 | 2019-01-29 | Regents of the University of Colorado, a body corp | Degradable thiol-ene polymers |
US9631092B2 (en) | 2001-10-10 | 2017-04-25 | Regents Of The University Of Colorado | Degradable thiol-ene polymers |
US7288608B2 (en) * | 2001-10-10 | 2007-10-30 | Regents Of The University Of Colorado | Degradable thiol-ene polymers |
US8519086B2 (en) | 2001-10-10 | 2013-08-27 | The Regents Of The University Of Colorado | Degradable thiol-ene polymers |
US8859716B2 (en) | 2001-10-10 | 2014-10-14 | The Regents Of The University Of Colorado | Degradable thiol-ene polymers |
US9987393B2 (en) | 2011-01-28 | 2018-06-05 | The Regents Of The University Of Colorado, A Body | Covalently cross linked hydrogels and methods of making and using same |
CN102888149A (en) * | 2011-07-20 | 2013-01-23 | 上海申悦油墨有限公司 | Novel NK white gravure ink |
CN102888148A (en) * | 2011-07-20 | 2013-01-23 | 上海申悦油墨有限公司 | Novel HS white gravure ink |
US10016505B2 (en) | 2012-02-02 | 2018-07-10 | Mosaic Biosciences, Inc. | Biomaterials for delivery of blood extracts and methods of using same |
US11160866B2 (en) | 2012-02-02 | 2021-11-02 | Mosaic Biosciences, Inc. | Biomaterials for delivery of blood extracts and methods of using same |
US9988433B2 (en) | 2013-03-14 | 2018-06-05 | Mosaic Biosciences, Inc. | Covalent modification of biological macromolecules |
US11130797B2 (en) | 2013-03-14 | 2021-09-28 | Mosaic Biosciences, Inc. | Covalent modification of biological macromolecules |
US10912837B2 (en) | 2015-02-09 | 2021-02-09 | Mosaic Biosciences, Inc. | Degradable thiol-ene polymers and methods of making thereof |
US11439711B2 (en) | 2015-02-09 | 2022-09-13 | Mosaic Biosciences, Inc. | Degradable thiol-ene polymers and methods of making thereof |
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