GB764299A - Improved polymers prepared from acrylonitrile - Google Patents
Improved polymers prepared from acrylonitrileInfo
- Publication number
- GB764299A GB764299A GB29091/53A GB2909153A GB764299A GB 764299 A GB764299 A GB 764299A GB 29091/53 A GB29091/53 A GB 29091/53A GB 2909153 A GB2909153 A GB 2909153A GB 764299 A GB764299 A GB 764299A
- Authority
- GB
- United Kingdom
- Prior art keywords
- vinyl
- dimethyl
- methyl
- per cent
- acrylonitrile
- 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
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04D—NON-POSITIVE-DISPLACEMENT PUMPS
- F04D25/00—Pumping installations or systems
- F04D25/02—Units comprising pumps and their driving means
- F04D25/08—Units comprising pumps and their driving means the working fluid being air, e.g. for ventilation
- F04D25/10—Units comprising pumps and their driving means the working fluid being air, e.g. for ventilation the unit having provisions for automatically changing direction of output air
- F04D25/105—Units comprising pumps and their driving means the working fluid being air, e.g. for ventilation the unit having provisions for automatically changing direction of output air by changing rotor axis direction, e.g. oscillating fans
-
- 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
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (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
Graft polymers are prepared by polymerizing in the presence of a catalyst, in solution or dispersion, from 5 to 95 parts of a monomer mixture consisting of from 85.0 to 99.5 per cent of acrylonitrile and from 15.0 to 0.5 per cent of a different, monoethylenically unsaturated compound containing a -CH=C< group and from 95 to 5 parts of an isolated polymer selected from (1), an isolated homopolymer of a compound represented by the following formul <FORM:0764299/IV(a)/1> (acrylamides) <FORM:0764299/IV(a)/2> (maleamides) <FORM:0764299/IV(a)/3> (fumaramides) <FORM:0764299/IV(a)/4> (itaconamides) <FORM:0764299/IV(a)/5> (citraconamides) <FORM:0764299/IV(a)/6> (maleamates) <FORM:0764299/IV(a)/7> (fumarates) <FORM:0764299/IV(a)/8> and <FORM:0764299/IV(a)/9> (itaconamates) <FORM:0764299/IV(a)/100> and <FORM:0764299/IV(a)/111> (citraconamates) <FORM:0764299/IV(a)/122> (acrylates) and <FORM:0764299/IV(a)/133> (vinyl carboxylic esters) wherein each R and R1 represents a hydrogen atom or an alkyl group containing from 1 to 4 carbon atoms, R2 represents an alkyl group containing from 1 to 4 carbon atoms, R3 represents a hydrogen atom or a methyl group and R4 represents an alkyl group containing from 1 to 3 carbon atoms, and (2) an isolated interpolymer of a different mixture of monomers of from 1 to 99 per cent of a compound represented by the above formul and from 99 to 1 per cent of a different compound represented by the above formul or acrylonitrile. Lists of monomers (1) are given in the Specification. Other compounds specified containing the -C=C< group are styrene, alpha-methyl styrene, p-acetaminostyrene, alpha-acetoxystyrene, vinyl and vinylidene chlorides, ethyl vinyl ether, isopropyl vinyl ether, ethyl isopropenyl ketone, methyl isopropenyl ketone, methyl vinyl ketone, ethyl vinyl ketone, dimethyl maleate, diethyl maleate, diisopropyl fumarate, fumaronitrile, methacrylonitrile, acrylic acid, methacrylic acid, N-vinyl phthalimide, vinyl sulphonamide, ethylene and isobutylene. Polymerization catalysts specified are benzoyl, lauryl, acetyl, acetyl benzoyl, oleoyl, triacetone and urea peroxides, t.-butyl hydroperoxide, alkyl percarbonates, sodium and potassium perborates and alkali metal and ammonium persulphates, and azines and ketazines. The persulphate catalysts may be used in conjunction with bisulphites. Polymerization may be carried out in organic solvents or aqueous acetonitrile or acetone, but is preferably effected in an aqueous medium in the presence or absence of emulsifiers such as sodium lauryl sulphate, sodium isobutylenenaphthalene sulphonate, sodium 7-ethyl-2-methyl undecane-4-sulphonate, alkali metal or amine addition salts of sulphosuccinic acid esters, alkali metal salts of fatty acids containing from 12 to 20 carbon atoms, sulphonated fatty acid amides, alkali metal salts of alkane sulphonic acids and sulphonated ethers. Also present in the reaction mixture may be chain regulators such as hexyl, octyl, lauryl, dodecyl and myristyl mercaptans. The polymers produced may be dissolved in various solvents, either alone or in admixture with polyacrylonitrile or copolymers containing at least 85 per cent of acrylonitrile, e.g. a copolymer with vinyl acetate, and the solutions used in the production of films and fibres. Solvents specified are dimethyl formamide, dimethyl acetamide, dimethyl cyanamide, dimethyl cyanoacetamide, dimethylbeta - cyanopropionamide, gamma - butyrolactone, N - methyl - 2 - pyrolidone, glyconitrile, malononitrile, ethylene cyanohydrin, ethylene carbonate, ethylene carbamate, dimethyl sulphoxide, dimethyl sulphone, tetramethylene sulphoxide, tetramethylene sulphone, N-formyl pyrolidine, N-formyl morpholine and tetramethylene methane phosphonamide. Specifications 764,296, 764,297 and 764,298 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US764299XA | 1952-10-21 | 1952-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB764299A true GB764299A (en) | 1956-12-28 |
Family
ID=22131952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB29091/53A Expired GB764299A (en) | 1952-10-21 | 1953-10-21 | Improved polymers prepared from acrylonitrile |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE523679A (en) |
DE (1) | DE1020458B (en) |
GB (1) | GB764299A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3008918A (en) * | 1958-01-29 | 1961-11-14 | Dow Chemical Co | Compositions comprising graft copolymers of certain sulfonated acrylate and acryloyl taurine type monomers on acrylonitrile polymer substrates |
US3242232A (en) * | 1962-06-22 | 1966-03-22 | Dow Chemical Co | Compositions comprising graft copolymers of certain monomers of polyglycol ethers ofalkenyl aromatics on polyolefin substrates and the method of making said compositions |
US3249655A (en) * | 1962-04-04 | 1966-05-03 | Dow Chemical Co | Compositions comprising graft copolymers of certain monomeric polyglycol ethers of alkenyl aromatics on acrylonitrile polymer substrates |
US3265655A (en) * | 1963-09-26 | 1966-08-09 | Union Carbide Corp | Polyvinyl acetate compositions |
US3274294A (en) * | 1962-06-22 | 1966-09-20 | Dow Chemical Co | Compositions comprising graft copolymers on polyester substrates of one or more monomers from the group including vinyl lactams, sulfonated alkenyl and/or alpha-halo alkenyl aromatics, sulfonated olefins, sulfonated acrylates and methacrylates, vinyl pyridines, aminated alkenyl aromatics, aminated acrylates and methacrylates, and monomericpolyglycol ethers of alkenyl aromatics |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL75532C (en) * | 1949-05-07 |
-
0
- BE BE523679D patent/BE523679A/xx unknown
-
1953
- 1953-09-19 DE DEE7838A patent/DE1020458B/en active Pending
- 1953-10-21 GB GB29091/53A patent/GB764299A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3008918A (en) * | 1958-01-29 | 1961-11-14 | Dow Chemical Co | Compositions comprising graft copolymers of certain sulfonated acrylate and acryloyl taurine type monomers on acrylonitrile polymer substrates |
US3249655A (en) * | 1962-04-04 | 1966-05-03 | Dow Chemical Co | Compositions comprising graft copolymers of certain monomeric polyglycol ethers of alkenyl aromatics on acrylonitrile polymer substrates |
US3242232A (en) * | 1962-06-22 | 1966-03-22 | Dow Chemical Co | Compositions comprising graft copolymers of certain monomers of polyglycol ethers ofalkenyl aromatics on polyolefin substrates and the method of making said compositions |
US3274294A (en) * | 1962-06-22 | 1966-09-20 | Dow Chemical Co | Compositions comprising graft copolymers on polyester substrates of one or more monomers from the group including vinyl lactams, sulfonated alkenyl and/or alpha-halo alkenyl aromatics, sulfonated olefins, sulfonated acrylates and methacrylates, vinyl pyridines, aminated alkenyl aromatics, aminated acrylates and methacrylates, and monomericpolyglycol ethers of alkenyl aromatics |
US3265655A (en) * | 1963-09-26 | 1966-08-09 | Union Carbide Corp | Polyvinyl acetate compositions |
Also Published As
Publication number | Publication date |
---|---|
BE523679A (en) | |
DE1020458B (en) | 1957-12-05 |
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