GB740720A - Chemical products - Google Patents
Chemical productsInfo
- Publication number
- GB740720A GB740720A GB16978/53A GB1697853A GB740720A GB 740720 A GB740720 A GB 740720A GB 16978/53 A GB16978/53 A GB 16978/53A GB 1697853 A GB1697853 A GB 1697853A GB 740720 A GB740720 A GB 740720A
- Authority
- GB
- United Kingdom
- Prior art keywords
- glycidyl
- copolymers
- vinyl
- alpha
- epoxy
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/3209—Epoxy compounds containing three or more epoxy groups obtained by polymerisation of unsaturated mono-epoxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Polyamine copolymers having an amino nitrogen content of from 0.3 to 10 per cent are prepared by reacting ammonia or a monoamine having at least one hydrogen atom bonded to a basic nitrogen atom and having an aliphatic or cycloaliphatic substituent containing 1 to 8 carbon atoms, with a copolymer of a monoethylenically unsaturated epoxymonomer and at least one other polymerizable vinylidene epoxy-free monomer, combined in a mol. ratio of 1 : 1 to 1 : 75, the copolymer having a molecular weight of at least 800 and an epoxide oxygen content of 0.4 to 0.8 per cent. Epoxy monomers specified are glycidyl acrylate, methacrylate, and sorbate, glycidyl vinyl phthalate, glycidyl allyl phthalate, glycidyl allyl maleate, glycidyl allyl ether, glycidyl vinyl ether, 1,2-epoxybutene-3, and allyl alpha, betaepoxyisovalerate. Copolymerizable monomers specified are butyl acrylate and methacrylate, methyl methacrylate, acrylonitrile, butadiene, chloroprene, vinyl acetate, vinyl ethers, styrene, and vinyl and vinylidene chlorides. Amines specified are mono- and di-methylamine, monoand di-ethylamine, isopropylamine, butylamine, amylamine, 2 - ethylhexylamine, cyclohexylamine, ethanolamine, and diethanolamine. The copolymers may be prepared in bulk, or solution in solvents such as benzene, dioxane, isopropyl alcohol, and methyl isobutyl ketone, with the aid of catalysts such as benzoyl peroxide, ditertiary butyl peroxide, and alpha, alpha-azodiisobutyronitrile, the copolymers preferably being in the form of oily viscous liquids with molecular weights of 1000 to 8000. The reaction between the epoxy copolymers and the ammonia or amines may be carried out at low, normal, or elevated temperatures in the presence or absence of an inert solvent such as benzene, dioxane, methyl ethyl ketone, or isopropyl alcohol. The after-treated polymers are soluble in dilute acids, such as carbonic, acetic, adipic, benzoic, oleic, drying oil, and castor oil acids, and may also be treated with formaldehyde. The polyamine copolymers may be used in coating, impregnating, and adhesive compositions, as dispersing agents for waxes and oils, and as binders for printing inks and paints. Specification 722,258 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US740720XA | 1952-06-23 | 1952-06-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB740720A true GB740720A (en) | 1955-11-16 |
Family
ID=22117535
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16978/53A Expired GB740720A (en) | 1952-06-23 | 1953-06-19 | Chemical products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB740720A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5710211A (en) * | 1995-08-01 | 1998-01-20 | Kuraray Co., Ltd. | Process for producing vinyl alcohol polymer |
ITBO20120066A1 (en) * | 2012-02-10 | 2013-08-11 | Consiglio Nazionale Ricerche | PROCEDURE FOR THE TREATMENT OF A POLYMER |
CN113582276A (en) * | 2021-08-05 | 2021-11-02 | 郑州卓而泰新材料科技有限公司 | Anti-carbonization agent and preparation method thereof |
-
1953
- 1953-06-19 GB GB16978/53A patent/GB740720A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5710211A (en) * | 1995-08-01 | 1998-01-20 | Kuraray Co., Ltd. | Process for producing vinyl alcohol polymer |
ITBO20120066A1 (en) * | 2012-02-10 | 2013-08-11 | Consiglio Nazionale Ricerche | PROCEDURE FOR THE TREATMENT OF A POLYMER |
WO2013118100A3 (en) * | 2012-02-10 | 2014-01-09 | Consiglio Nazionale Delle Ricerche | Process for the treatment of a polymer |
CN113582276A (en) * | 2021-08-05 | 2021-11-02 | 郑州卓而泰新材料科技有限公司 | Anti-carbonization agent and preparation method thereof |
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