JPS5871928A - 熱可塑性、非架橋無水物ポリマ−、イミドポリマ−、およびその製造方法 - Google Patents
熱可塑性、非架橋無水物ポリマ−、イミドポリマ−、およびその製造方法Info
- Publication number
- JPS5871928A JPS5871928A JP57175448A JP17544882A JPS5871928A JP S5871928 A JPS5871928 A JP S5871928A JP 57175448 A JP57175448 A JP 57175448A JP 17544882 A JP17544882 A JP 17544882A JP S5871928 A JPS5871928 A JP S5871928A
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- ammonia
- psi
- units
- imide
- 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.)
- Granted
Links
- 229920000642 polymer Polymers 0.000 title claims description 82
- 150000003949 imides Chemical class 0.000 title claims description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 229920001169 thermoplastic Polymers 0.000 title claims description 4
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 39
- 150000008064 anhydrides Chemical class 0.000 claims description 21
- 229910021529 ammonia Inorganic materials 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 16
- 238000000926 separation method Methods 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 14
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 11
- 238000000354 decomposition reaction Methods 0.000 claims description 10
- 239000000178 monomer Substances 0.000 claims description 9
- 239000004202 carbamide Substances 0.000 claims description 8
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical group O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 7
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- 239000003039 volatile agent Substances 0.000 claims description 6
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical class NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 239000007789 gas Substances 0.000 claims description 3
- 238000006467 substitution reaction Methods 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 150000003672 ureas Chemical class 0.000 claims description 2
- 229920006037 cross link polymer Polymers 0.000 claims 2
- ATMLPEJAVWINOF-UHFFFAOYSA-N acrylic acid acrylic acid Chemical compound OC(=O)C=C.OC(=O)C=C ATMLPEJAVWINOF-UHFFFAOYSA-N 0.000 claims 1
- 238000001125 extrusion Methods 0.000 claims 1
- 238000006358 imidation reaction Methods 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 19
- 239000002253 acid Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 9
- 239000000155 melt Substances 0.000 description 7
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 6
- 229910052753 mercury Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 150000003141 primary amines Chemical class 0.000 description 5
- 229920006351 engineering plastic Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000005395 methacrylic acid group Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical class CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical class COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- -1 stearyl methacrylate Chemical compound 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- GXZPMXGRNUXGHN-UHFFFAOYSA-N 1-ethenoxy-2-methoxyethane Chemical compound COCCOC=C GXZPMXGRNUXGHN-UHFFFAOYSA-N 0.000 description 1
- NSOAQRMLVFRWIT-UHFFFAOYSA-N 1-ethenoxydecane Chemical compound CCCCCCCCCCOC=C NSOAQRMLVFRWIT-UHFFFAOYSA-N 0.000 description 1
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 description 1
- AOUSBQVEVZBMNI-UHFFFAOYSA-N 2-bromoethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCBr AOUSBQVEVZBMNI-UHFFFAOYSA-N 0.000 description 1
- CDZAAIHWZYWBSS-UHFFFAOYSA-N 2-bromoethyl prop-2-enoate Chemical compound BrCCOC(=O)C=C CDZAAIHWZYWBSS-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- KFTHUBZIEMOORC-UHFFFAOYSA-N 2-methylbut-2-enamide Chemical compound CC=C(C)C(N)=O KFTHUBZIEMOORC-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical class CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- COCLLEMEIJQBAG-UHFFFAOYSA-N 8-methylnonyl 2-methylprop-2-enoate Chemical class CC(C)CCCCCCCOC(=O)C(C)=C COCLLEMEIJQBAG-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical class CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000011074 autoclave method Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical class CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical class CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical class CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- MGJXBDMLVWIYOQ-UHFFFAOYSA-N methylazanide Chemical group [NH-]C MGJXBDMLVWIYOQ-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- YRVUCYWJQFRCOB-UHFFFAOYSA-N n-butylprop-2-enamide Chemical compound CCCCNC(=O)C=C YRVUCYWJQFRCOB-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Chemical class CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
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
-
- 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
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
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)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30929881A | 1981-10-07 | 1981-10-07 | |
| US309298 | 1981-10-07 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5871928A true JPS5871928A (ja) | 1983-04-28 |
| JPH0463901B2 JPH0463901B2 (cg-RX-API-DMAC7.html) | 1992-10-13 |
Family
ID=23197601
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57175448A Granted JPS5871928A (ja) | 1981-10-07 | 1982-10-07 | 熱可塑性、非架橋無水物ポリマ−、イミドポリマ−、およびその製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0076691B2 (cg-RX-API-DMAC7.html) |
| JP (1) | JPS5871928A (cg-RX-API-DMAC7.html) |
| CA (1) | CA1231500A (cg-RX-API-DMAC7.html) |
| DE (1) | DE3273211D1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES8401100A1 (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA827343B (cg-RX-API-DMAC7.html) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60136791A (ja) * | 1983-12-05 | 1985-07-20 | 旭化成株式会社 | 照明器 |
| JPS60138803A (ja) * | 1983-12-05 | 1985-07-23 | 旭化成株式会社 | 表示器 |
| JPS60233106A (ja) * | 1984-05-07 | 1985-11-19 | Toray Ind Inc | 光学ディスク材料の製造法 |
| JPS6143604A (ja) * | 1984-08-08 | 1986-03-03 | Asahi Chem Ind Co Ltd | 変性共重合体の製造方法 |
| JPS6147707A (ja) * | 1984-08-13 | 1986-03-08 | Asahi Chem Ind Co Ltd | 耐熱共重合体 |
| JPS6289705A (ja) * | 1985-08-27 | 1987-04-24 | ロ−ム・アンド・ハ−ス・カンパニ− | イミドポリマ− |
| JP2008106248A (ja) * | 2006-09-26 | 2008-05-08 | Toray Ind Inc | 熱可塑性共重合体の製造方法 |
| JP2011099112A (ja) * | 2002-08-02 | 2011-05-19 | Three M Innovative Properties Co | ポリマー材料の変性方法および得られる組成物 |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5004777A (en) * | 1985-08-27 | 1991-04-02 | Rohm And Haas Company | Imide polymers |
| US5264483A (en) * | 1985-08-27 | 1993-11-23 | Rohm And Haas Company | Imide polymers |
| CA1279747C (en) * | 1986-01-23 | 1991-01-29 | Hisao Anzai | Methacrylate resin composition and process for its preparation |
| CA1274936A (en) * | 1986-12-25 | 1990-10-02 | Akihiro Watanabe | Random copolymer containing hexagonal imide units, a process for producing the same, and an optical disc substrate made of the random copolymer |
| FR2618440B1 (fr) * | 1987-07-20 | 1990-06-22 | Acome Soc Coop Travailleurs | Materiau polymere insoluble a sites reactifs condenses, notamment du type groupe anhydride ou ester actif, procede de preparation de ce materiau polymere et application de ce materiau |
| JPH01103612A (ja) * | 1987-07-30 | 1989-04-20 | Sumitomo Chem Co Ltd | 熱可塑性共重合体 |
| US5096977A (en) * | 1987-08-12 | 1992-03-17 | Atochem North America, Inc. | Process for preparing polymer bound UV stabilizers |
| US4866136A (en) * | 1987-08-12 | 1989-09-12 | Pennwalt Corporation | Process for producing polymer bound hindered amine light stabilizers |
| US5206378A (en) * | 1987-08-12 | 1993-04-27 | Elf Atochem North America, Inc. | Hydrazido functionalized 2-(2-hydroxyphenyl)-2h-benzotriazoles |
| US4975489A (en) * | 1987-08-12 | 1990-12-04 | Atochem North America, Inc. | Process for preparing polymer bound hindered amine light stabilizers |
| US4857595A (en) * | 1987-08-12 | 1989-08-15 | Pennwalt Corporation | Polymer bound hindered amine light stabilizers |
| US4981915A (en) * | 1987-08-12 | 1991-01-01 | Atochem North America, Inc. | Multipurpose polymer bound stabilizers |
| US4863999A (en) * | 1987-08-12 | 1989-09-05 | Pennwalt Corporation | Multipurpose polymer bound stabilizers |
| US5096974A (en) * | 1987-08-12 | 1992-03-17 | Atochem North America, Inc. | Process for preparing multipurpose polymer bound stabilizers and polymer bound stabilizer produced thereby |
| US4868246A (en) * | 1987-08-12 | 1989-09-19 | Pennwalt Corporation | Polymer bound UV stabilizers |
| US4981917A (en) * | 1987-08-12 | 1991-01-01 | Atochem North America, Inc. | Process for preparing polymer bound antioxidant stabilizers |
| US4857596A (en) * | 1987-08-12 | 1989-08-15 | Pennwalt Corporation | Polymer bound antioxidant stabilizers |
| US4981914A (en) * | 1987-08-12 | 1991-01-01 | Atochem North America, Inc. | Polymer bound UV stabilizers |
| US4874824A (en) * | 1987-11-23 | 1989-10-17 | Rohm And Haas Company | Process for manufacturing low-acid, glutaric-anhydride-containing copolymers |
| US5218068A (en) * | 1988-03-25 | 1993-06-08 | The Dow Chemical Company | Intrinsically low birefringent molding polymers and optical storage disks therefrom |
| US5272219A (en) * | 1988-08-18 | 1993-12-21 | Elf Atochem North America, Inc. | Process for preparing amino or hydrazino peroxides, derivatives and their uses |
| US4956416A (en) * | 1988-08-18 | 1990-09-11 | Atochem North America, Inc. | Amino or hydrazino peroxides, derivatives and their uses |
| US5286793A (en) * | 1992-06-15 | 1994-02-15 | Istituto Guido Donegani | In situ compatibilization of PPE/polyethylene copolymer blends |
| US6370911B1 (en) | 1999-08-13 | 2002-04-16 | Air Liquide America Corporation | Nitrous oxide purification system and process |
| US6858672B2 (en) | 2002-06-20 | 2005-02-22 | Basell Poliolefine Italia S.P.A. | Safe process for making polymers containing N-phenylimide groups |
| DE102006032225A1 (de) * | 2006-07-07 | 2008-01-10 | Belland Ag | Anhydritisiertes Copolymer |
| EP2065410A4 (en) * | 2006-09-20 | 2012-08-08 | Toray Industries | PROCESS FOR PREPARING THERMOPLASTIC COPOLYMER |
| WO2016105947A1 (en) * | 2014-12-22 | 2016-06-30 | Dow Global Technologies Llc | Polymethacrylic imide-acid polymers and methods of making and using |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4985184A (cg-RX-API-DMAC7.html) * | 1972-08-14 | 1974-08-15 | ||
| JPS5580459A (en) * | 1978-12-08 | 1980-06-17 | Rohm & Haas | Polyglutarimide composition |
| JPS55152740A (en) * | 1979-05-07 | 1980-11-28 | Rohm & Haas | Polyglytarimide impact strength improvement |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2146209A (en) † | 1936-07-31 | 1939-02-07 | Du Pont | Preparation of resinous imides of substituted acrylic acids |
| NL213287A (cg-RX-API-DMAC7.html) * | 1955-12-27 | |||
| DE1088231B (de) † | 1958-03-22 | 1960-09-01 | Roehm & Haas Gmbh | Verfahren zur Herstellung Stickstoff enthaltender Derivate der Polymethacrylsaeure |
| DE1195952B (de) † | 1961-03-22 | 1965-07-01 | Roehm & Haas Gmbh | Verfahren zur Herstellung von Polymethacrylsaeureimiden |
| US4169924A (en) * | 1977-06-09 | 1979-10-02 | Gaf Corporation | Preparation of linear cyclic polyimides from latices |
| US4246374A (en) † | 1979-04-23 | 1981-01-20 | Rohm And Haas Company | Imidized acrylic polymers |
-
1982
- 1982-09-30 CA CA000412580A patent/CA1231500A/en not_active Expired
- 1982-10-05 DE DE8282305285T patent/DE3273211D1/de not_active Expired
- 1982-10-05 EP EP82305285A patent/EP0076691B2/en not_active Expired - Lifetime
- 1982-10-07 ES ES516331A patent/ES8401100A1/es not_active Expired
- 1982-10-07 JP JP57175448A patent/JPS5871928A/ja active Granted
- 1982-10-07 ZA ZA827343A patent/ZA827343B/xx unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4985184A (cg-RX-API-DMAC7.html) * | 1972-08-14 | 1974-08-15 | ||
| JPS5580459A (en) * | 1978-12-08 | 1980-06-17 | Rohm & Haas | Polyglutarimide composition |
| JPS55152740A (en) * | 1979-05-07 | 1980-11-28 | Rohm & Haas | Polyglytarimide impact strength improvement |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60136791A (ja) * | 1983-12-05 | 1985-07-20 | 旭化成株式会社 | 照明器 |
| JPS60138803A (ja) * | 1983-12-05 | 1985-07-23 | 旭化成株式会社 | 表示器 |
| JPS60233106A (ja) * | 1984-05-07 | 1985-11-19 | Toray Ind Inc | 光学ディスク材料の製造法 |
| JPS6143604A (ja) * | 1984-08-08 | 1986-03-03 | Asahi Chem Ind Co Ltd | 変性共重合体の製造方法 |
| JPS6147707A (ja) * | 1984-08-13 | 1986-03-08 | Asahi Chem Ind Co Ltd | 耐熱共重合体 |
| JPS6289705A (ja) * | 1985-08-27 | 1987-04-24 | ロ−ム・アンド・ハ−ス・カンパニ− | イミドポリマ− |
| JP2011099112A (ja) * | 2002-08-02 | 2011-05-19 | Three M Innovative Properties Co | ポリマー材料の変性方法および得られる組成物 |
| JP2008106248A (ja) * | 2006-09-26 | 2008-05-08 | Toray Ind Inc | 熱可塑性共重合体の製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1231500A (en) | 1988-01-12 |
| JPH0463901B2 (cg-RX-API-DMAC7.html) | 1992-10-13 |
| DE3273211D1 (en) | 1986-10-16 |
| ES516331A0 (es) | 1983-11-16 |
| EP0076691B2 (en) | 1993-11-18 |
| ES8401100A1 (es) | 1983-11-16 |
| EP0076691A1 (en) | 1983-04-13 |
| EP0076691B1 (en) | 1986-09-10 |
| ZA827343B (en) | 1983-12-28 |
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