JP5058407B2 - 場合によりエチレン性不飽和ニトリルを含有した、ビニル芳香族ポリマーの生産プロセス - Google Patents
場合によりエチレン性不飽和ニトリルを含有した、ビニル芳香族ポリマーの生産プロセス Download PDFInfo
- Publication number
- JP5058407B2 JP5058407B2 JP2000364891A JP2000364891A JP5058407B2 JP 5058407 B2 JP5058407 B2 JP 5058407B2 JP 2000364891 A JP2000364891 A JP 2000364891A JP 2000364891 A JP2000364891 A JP 2000364891A JP 5058407 B2 JP5058407 B2 JP 5058407B2
- Authority
- JP
- Japan
- Prior art keywords
- reactor
- vinyl aromatic
- pfr
- ethylenically unsaturated
- tubular reactor
- 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 - Lifetime
Links
- 229920000642 polymer Polymers 0.000 title claims description 25
- 229920002554 vinyl polymer Polymers 0.000 title claims description 20
- 238000000034 method Methods 0.000 title claims description 14
- 150000002825 nitriles Chemical class 0.000 title claims description 6
- 239000000178 monomer Substances 0.000 claims description 25
- 239000011541 reaction mixture Substances 0.000 claims description 13
- 238000004064 recycling Methods 0.000 claims description 12
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 8
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000010924 continuous production Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 8
- 238000009826 distribution Methods 0.000 description 7
- 239000003999 initiator Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 229920000638 styrene acrylonitrile Polymers 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 4
- YSPDISPRPJFBCV-UHFFFAOYSA-N 1-phenyl-1,2,3,4-tetrahydronaphthalene Chemical compound C12=CC=CC=C2CCCC1C1=CC=CC=C1 YSPDISPRPJFBCV-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- -1 ethylene, propylene, maleic anhydride Chemical class 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- MMSLOZQEMPDGPI-UHFFFAOYSA-N p-Mentha-1,3,5,8-tetraene Chemical compound CC(=C)C1=CC=C(C)C=C1 MMSLOZQEMPDGPI-UHFFFAOYSA-N 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- AUHKVLIZXLBQSR-UHFFFAOYSA-N 1,2-dichloro-3-(1,2,2-trichloroethenyl)benzene Chemical compound ClC(Cl)=C(Cl)C1=CC=CC(Cl)=C1Cl AUHKVLIZXLBQSR-UHFFFAOYSA-N 0.000 description 1
- VTPNYMSKBPZSTF-UHFFFAOYSA-N 1-ethenyl-2-ethylbenzene Chemical compound CCC1=CC=CC=C1C=C VTPNYMSKBPZSTF-UHFFFAOYSA-N 0.000 description 1
- WHFHDVDXYKOSKI-UHFFFAOYSA-N 1-ethenyl-4-ethylbenzene Chemical compound CCC1=CC=C(C=C)C=C1 WHFHDVDXYKOSKI-UHFFFAOYSA-N 0.000 description 1
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 1
- 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 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 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
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/18—Stationary reactors having moving elements inside
- B01J19/1812—Tubular reactors
- B01J19/1837—Loop-type reactors
-
- 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
- C08F257/00—Macromolecular compounds obtained by polymerising monomers on to polymers of aromatic monomers as defined in group C08F12/00
-
- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/08—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of nitriles
-
- 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
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
- C08F279/04—Vinyl aromatic monomers and nitriles as the only monomers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00002—Chemical plants
- B01J2219/00027—Process aspects
- B01J2219/00033—Continuous processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
- B01J2219/00076—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements inside the reactor
- B01J2219/00081—Tubes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00164—Controlling or regulating processes controlling the flow
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silicon Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT1999MI002535A IT1314260B1 (it) | 1999-12-03 | 1999-12-03 | Procedimento per la produzione di polimeri vinilaromaticieventualmente contenenti un nitrile etilenicamente insaturo. |
| IT99A002535 | 1999-12-03 | ||
| ITMI99A002535 | 1999-12-03 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2001192403A JP2001192403A (ja) | 2001-07-17 |
| JP5058407B2 true JP5058407B2 (ja) | 2012-10-24 |
Family
ID=11384069
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000364891A Expired - Lifetime JP5058407B2 (ja) | 1999-12-03 | 2000-11-30 | 場合によりエチレン性不飽和ニトリルを含有した、ビニル芳香族ポリマーの生産プロセス |
Country Status (15)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102050928B (zh) * | 2009-10-30 | 2012-07-18 | 中国石油天然气股份有限公司 | 一种阻燃abs的连续本体合成方法 |
| RU2607521C2 (ru) * | 2012-09-26 | 2017-01-10 | Басф Се | Способ получения полимеров |
| WO2016045020A1 (zh) * | 2014-09-24 | 2016-03-31 | 中国纺织科学研究院 | 交换反应系统、包含其的改性聚酯生产系统、改性聚酯生产方法及改性聚酯纤维产品 |
| TR201900627A2 (tr) | 2019-01-15 | 2020-08-21 | Aksa Akrilik Kimya Sanayii Anonim Sirketi | Bi̇r modakri̇li̇k poli̇meri̇ üretmek üzere bi̇r reaktör si̇stemi̇ ve i̇lgi̇li̇ poli̇mer üreti̇m yöntemi̇ |
| IT202100017519A1 (it) * | 2021-07-02 | 2023-01-02 | Versalis Spa | Procedimento per la preparazione di polimeri vinilaromatici. |
| CN113583186A (zh) * | 2021-09-09 | 2021-11-02 | 科元控股集团有限公司 | 一种连续本体abs树脂的生产方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL88611C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1951-09-10 | |||
| US2989517A (en) * | 1954-05-06 | 1961-06-20 | Dow Chemical Co | Polymerization method |
| NL7700412A (nl) * | 1977-01-15 | 1978-07-18 | Synres Internationaal Nv | Continu bereiding van polymeren in de massa. |
| DE2724360C3 (de) * | 1977-05-28 | 1988-03-24 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von thermoplastischen Formmassen auf Basis von Vinylpolymerisaten |
| DE3750561T2 (de) * | 1986-07-25 | 1995-03-02 | Dainippon Ink & Chemicals | Verfahren zur Herstellung von schlagfesten Polystyrenharzen durch kontinuierliche Massepolymerisation. |
| JPH0725857B2 (ja) * | 1986-07-31 | 1995-03-22 | 大日本インキ化学工業株式会社 | 耐衝撃性スチレン系樹脂の連続塊状重合法 |
| JPH07116262B2 (ja) * | 1987-01-20 | 1995-12-13 | 三井東圧化学株式会社 | α−メチルスチレン共重合体の製造方法 |
| IT1218559B (it) * | 1987-04-07 | 1990-04-19 | Montedipe Spa | Processo per la produzione in soluzione e in continuo di resine termoplastiche stireniche |
| JP2560342B2 (ja) * | 1987-09-11 | 1996-12-04 | 大日本インキ化学工業株式会社 | スチレン系樹脂の連続塊状重合法 |
| DE68925874T2 (de) * | 1988-12-12 | 1996-08-29 | Dainippon Ink & Chemicals | Kontinuierliches Massen-Polymerisationsverfahren zur Herstellung von Styrol-Polymeren |
| IT1230085B (it) * | 1989-05-24 | 1991-10-05 | Montedipe Spa | Processo per la produzione in massa e in continuo di (co) polimeri vinil aromatici antiurto. |
| US5256732A (en) * | 1990-08-13 | 1993-10-26 | Dainippon Ink And Chemicals, Inc. | Method for the continuous bulk polymerization for impact resistant styrene resin |
| JP2636970B2 (ja) * | 1991-02-27 | 1997-08-06 | 出光石油化学株式会社 | スチレン系重合体の製造方法 |
| DE19524182A1 (de) * | 1995-07-03 | 1997-01-09 | Basf Ag | Verfahren und Vorrichtung zur kontinuierlichen Herstellung von Polymeren |
| DE19618678A1 (de) * | 1996-05-09 | 1997-11-13 | Basf Ag | Verfahren zur Herstellung von Polystyrol durch kontinuierliche anionische Polymerisation |
| IT1284599B1 (it) * | 1996-09-27 | 1998-05-21 | Enichem Spa | Procedimento per la preparazione di polimeri vinilaromatici rinforzati con gomma |
| ITMI981156A1 (it) | 1998-05-26 | 1999-11-26 | Enichem Spa | Composizioni polimeriche |
| WO1999062976A1 (fr) * | 1998-06-04 | 1999-12-09 | Asahi Kasei Kogyo Kabushiki Kaisha | Procede de preparation de resine de styrene renforcee par du caoutchouc |
-
1999
- 1999-12-03 IT IT1999MI002535A patent/IT1314260B1/it active
-
2000
- 2000-11-21 CA CA2326907A patent/CA2326907C/en not_active Expired - Lifetime
- 2000-11-28 EP EP00204226.5A patent/EP1106631B1/en not_active Expired - Lifetime
- 2000-11-28 ES ES00204226T patent/ES2433009T3/es not_active Expired - Lifetime
- 2000-11-28 PL PL344149A patent/PL204237B1/pl unknown
- 2000-11-30 US US09/725,567 patent/US6348549B2/en not_active Expired - Lifetime
- 2000-11-30 CZ CZ20004452A patent/CZ300316B6/cs not_active IP Right Cessation
- 2000-11-30 RU RU2000129874/04A patent/RU2209214C2/ru active
- 2000-11-30 HR HRP20000828AA patent/HRP20000828B1/hr not_active IP Right Cessation
- 2000-11-30 JP JP2000364891A patent/JP5058407B2/ja not_active Expired - Lifetime
- 2000-12-01 BR BRPI0005682-0A patent/BR0005682B1/pt not_active IP Right Cessation
- 2000-12-01 HU HU0004781A patent/HU222655B1/hu active IP Right Grant
- 2000-12-01 TR TR2000/03585A patent/TR200003585A3/tr unknown
- 2000-12-01 AR ARP000106350A patent/AR026686A1/es active IP Right Grant
- 2000-12-01 NO NO20006132A patent/NO337551B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| US6348549B2 (en) | 2002-02-19 |
| TR200003585A2 (tr) | 2001-09-21 |
| HUP0004781A2 (hu) | 2001-07-30 |
| ITMI992535A1 (it) | 2001-06-03 |
| US20010005740A1 (en) | 2001-06-28 |
| EP1106631B1 (en) | 2013-08-21 |
| NO337551B1 (no) | 2016-05-09 |
| AR026686A1 (es) | 2003-02-19 |
| HRP20000828A2 (en) | 2001-06-30 |
| CA2326907A1 (en) | 2001-06-03 |
| JP2001192403A (ja) | 2001-07-17 |
| CA2326907C (en) | 2010-04-27 |
| CZ20004452A3 (cs) | 2001-07-11 |
| CZ300316B6 (cs) | 2009-04-15 |
| PL204237B1 (pl) | 2009-12-31 |
| HUP0004781A3 (en) | 2002-03-28 |
| HU222655B1 (hu) | 2003-09-29 |
| ES2433009T3 (es) | 2013-12-05 |
| RU2209214C2 (ru) | 2003-07-27 |
| HRP20000828B1 (hr) | 2014-03-14 |
| NO20006132D0 (no) | 2000-12-01 |
| IT1314260B1 (it) | 2002-12-06 |
| TR200003585A3 (tr) | 2001-09-21 |
| PL344149A1 (en) | 2001-06-04 |
| BR0005682B1 (pt) | 2010-12-28 |
| NO20006132L (no) | 2001-06-05 |
| BR0005682A (pt) | 2001-07-31 |
| HU0004781D0 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2001-02-28 |
| ITMI992535A0 (it) | 1999-12-03 |
| EP1106631A1 (en) | 2001-06-13 |
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