SU300482A1 - - Google Patents
Info
- Publication number
- SU300482A1 SU300482A1 SU1300115A SU1300115A SU300482A1 SU 300482 A1 SU300482 A1 SU 300482A1 SU 1300115 A SU1300115 A SU 1300115A SU 1300115 A SU1300115 A SU 1300115A SU 300482 A1 SU300482 A1 SU 300482A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- weight
- methacrylate
- thioalkyl
- polymers
- acrylic
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 claims description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 6
- -1 thioalkyl acrylate Chemical compound 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000011521 glass Substances 0.000 description 8
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 230000004580 weight loss Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- 101100465058 Caenorhabditis elegans prk-2 gene Proteins 0.000 description 1
- 239000004159 Potassium persulphate Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- FFYWKOUKJFCBAM-UHFFFAOYSA-N ethenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC=C FFYWKOUKJFCBAM-UHFFFAOYSA-N 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- XBTYSBUGTSUGJM-UHFFFAOYSA-N methyl prop-2-enoate;sodium Chemical compound [Na].COC(=O)C=C XBTYSBUGTSUGJM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 235000019394 potassium persulphate Nutrition 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU300482A1 true SU300482A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH089602B2 (ja) | ラジカル重合可能なuv‐吸収化合物及びその製造法 | |
| JP2573944B2 (ja) | 熱可塑性に加工可能なポリメタクリレ−ト成形材料及びその製法 | |
| JPH0216922B2 (enrdf_load_stackoverflow) | ||
| US4260768A (en) | Copolymerizable, ultraviolet light absorber 2-(2H-benzotriazol-2-yl)-4-alkylphenol acrylic acid esters | |
| US20120172563A1 (en) | Homopolymers and copolymers of hydroxyisobutyric acid (ester) (meth)acrylates | |
| SU300482A1 (enrdf_load_stackoverflow) | ||
| US2861051A (en) | Cross-linked graft copolymers of acrylonitrile and polyvinyl alcohols and method of preparing same | |
| US2727021A (en) | Polymerizable and polymerized aminoethyl acrylate-acrylonitrile compositions | |
| US3243416A (en) | 2-norbornylmethyl sters of acrylic and methacrylic acids and polymers thereof | |
| US2378535A (en) | Monomeric and polymeric esters of vinyl thiols and process for their manufacture | |
| US3197447A (en) | Polymers and copolymers of acetals of allyl alcohol | |
| US2906741A (en) | Polymerizable organic sulfides | |
| US4095019A (en) | Free radical polymerization process utilizing novel initiators | |
| US3634367A (en) | Thermally stabilized acrylic polymers | |
| US3143535A (en) | 2, 3-dibromohexahydro-4, 7-methanoindan-5-yl acrylate and methacrylate and polymers thereof | |
| JP3580908B2 (ja) | 透明耐熱性樹脂 | |
| US3649604A (en) | Novel method for polymerizing vinyl compounds in the presence of imidazole and a carbon tetrahalide | |
| SU218432A1 (ru) | Способ получения термостойких сополимеров | |
| GB2149414A (en) | Moulding compositions for optically readable data carriers | |
| JPS60231704A (ja) | ポリシロキサングラフト型変性ポリビニルアルコ−ル系共重合体の製法 | |
| US3260709A (en) | Copolymers of cyano-containing compounds | |
| US4349649A (en) | Process of preparing copolymers of butyl acrylate and 1-(α-alkyl acrylate)-1-tert-butyl peroxy ethanes | |
| US3528951A (en) | Copolymerization of acrylonitrile | |
| JPS62250004A (ja) | 熱成形安定の成形材料の製造方法 | |
| RU2734241C1 (ru) | Способ получения сополимеров акрилонитрила в растворе |