GB878926A - Improvements in and relating to polymers - Google Patents
Improvements in and relating to polymersInfo
- Publication number
- GB878926A GB878926A GB10489/59A GB1048959A GB878926A GB 878926 A GB878926 A GB 878926A GB 10489/59 A GB10489/59 A GB 10489/59A GB 1048959 A GB1048959 A GB 1048959A GB 878926 A GB878926 A GB 878926A
- Authority
- GB
- United Kingdom
- Prior art keywords
- anhydride
- group
- carbon atoms
- polymer
- groups
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- General 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)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A composition comprises the reaction product of a polymer containing a major proportion of anhydride units of the structure: <FORM:0878926/IV (a)/1> where R1 is hydrogen, chlorine, fluorine or bromine while R is R1 or a cyano group, an alkyl group having from 1-10 carbon atoms, an aryl group, an alkaryl group or an aralkyl group with (1) at least 20 mole per cent based on the anhydride groups of an amine of formula: <FORM:0878926/IV (a)/2> where X and Y are hydrogen or a hydrocarbon having from 1-20 carbon atoms, the product containing amide groups so interspersed on the main polymer chain that not more than one acyl group of each anhydride group on the parent anhydride polymer is converted to an amide linkage or (2) at least 20 mole per cent of an alcohol of formula X-OH where X is a hydrocarbon group of 1-20 carbon atoms or a tertiary amino hydrocarbon group having from 4-20 carbon atoms, the product containing ester groups so interspersed on the main polymer chain that not more than two adjacent carboxyl groups are converted to ester linkages, or a combination of (1) and (2). The polymer may be prepared by reacting the main anhydride polymer with an alcohol phenol, amine or ammonia at up to 100 DEG C. in an inert organic liquid, e.g. benzene, a halogenated hydrocarbon, dimethylformamide or a dimethyl-sulphoxide. The preferred anhydrides are those from acrylic and methacrylic acids or their alpha-substituted derivatives. The anhydride may be reacted with more than one of the above compounds, e.g. first with an alcohol to convert a portion of the anhydride groups to esters and then with an amine. Specified alcohols include methanol, secoctanols, phenol, hydroquinone, alpha and betanaphthols, ethylene glycol, erythritols, starch, cellulose, dimethylaminoethanol, 3-nitroprcpanol, while amines include methyl amine, aniline, mesitylene, n-methylaniline, and tolylene diamines. Specification 849,669 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US878926XA | 1958-03-31 | 1958-03-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB878926A true GB878926A (en) | 1961-10-04 |
Family
ID=22207888
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10489/59A Expired GB878926A (en) | 1958-03-31 | 1959-03-26 | Improvements in and relating to polymers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB878926A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0154177A2 (en) * | 1984-02-17 | 1985-09-11 | Bayer Ag | Copolymers based on maleic anhydride and alpha-, beta-unsaturated compounds, process for their manufacture and their use as paraffin inhibitors |
WO2003095507A1 (en) * | 2002-05-10 | 2003-11-20 | Ucb, S.A. | Water-dilutable/dispersible radiation curable compositions |
WO2003095506A1 (en) * | 2002-05-10 | 2003-11-20 | Ucb, S.A. | Radiation curable compositions |
CN113457564A (en) * | 2021-07-07 | 2021-10-01 | 贵州省材料产业技术研究院 | Esterified SMA (styrene maleic anhydride) modified quaternary ammonium phosphonium salt high-molecular antibacterial surfactant and application thereof |
-
1959
- 1959-03-26 GB GB10489/59A patent/GB878926A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0154177A2 (en) * | 1984-02-17 | 1985-09-11 | Bayer Ag | Copolymers based on maleic anhydride and alpha-, beta-unsaturated compounds, process for their manufacture and their use as paraffin inhibitors |
EP0154177A3 (en) * | 1984-02-17 | 1986-02-12 | Bayer Ag | Copolymers based on maleic anhydride and alpha-, beta-unsaturated compounds, process for their manufacture and their use as paraffin inhibitors |
US4670516A (en) * | 1984-02-17 | 1987-06-02 | Bayer Aktiengesellschaft | Copolymers based on maleic anhydride and α, β-unsaturated compounds a process for their preparation and their use as paraffin inhibitors |
WO2003095507A1 (en) * | 2002-05-10 | 2003-11-20 | Ucb, S.A. | Water-dilutable/dispersible radiation curable compositions |
WO2003095506A1 (en) * | 2002-05-10 | 2003-11-20 | Ucb, S.A. | Radiation curable compositions |
CN113457564A (en) * | 2021-07-07 | 2021-10-01 | 贵州省材料产业技术研究院 | Esterified SMA (styrene maleic anhydride) modified quaternary ammonium phosphonium salt high-molecular antibacterial surfactant and application thereof |
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