DE3938927C2 - - Google Patents
Info
- Publication number
- DE3938927C2 DE3938927C2 DE3938927A DE3938927A DE3938927C2 DE 3938927 C2 DE3938927 C2 DE 3938927C2 DE 3938927 A DE3938927 A DE 3938927A DE 3938927 A DE3938927 A DE 3938927A DE 3938927 C2 DE3938927 C2 DE 3938927C2
- Authority
- DE
- Germany
- Prior art keywords
- block
- blocks
- copolymers
- ethylene
- copolymer
- 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
- 229920001577 copolymer Polymers 0.000 claims description 39
- 229920000642 polymer Polymers 0.000 claims description 31
- 238000005984 hydrogenation reaction Methods 0.000 claims description 21
- 239000000178 monomer Substances 0.000 claims description 18
- 239000003054 catalyst Substances 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 238000006116 polymerization reaction Methods 0.000 claims description 9
- 229920002554 vinyl polymer Polymers 0.000 claims description 9
- 239000004793 Polystyrene Substances 0.000 claims description 8
- 150000001993 dienes Chemical class 0.000 claims description 8
- 229920002223 polystyrene Polymers 0.000 claims description 7
- 229920005684 linear copolymer Polymers 0.000 claims description 6
- 229920001897 terpolymer Polymers 0.000 claims description 4
- 238000010550 living polymerization reaction Methods 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 229920006216 polyvinyl aromatic Polymers 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000002897 diene group Chemical group 0.000 claims 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 26
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 19
- 229920001400 block copolymer Polymers 0.000 description 17
- 239000000243 solution Substances 0.000 description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 11
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- 239000001257 hydrogen Substances 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
- 239000005062 Polybutadiene Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 229920002857 polybutadiene Polymers 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- AQWSFUIGRSMCST-UHFFFAOYSA-N 3-pyridin-3-ylsulfonyl-5-(trifluoromethyl)chromen-2-one Chemical compound N1=CC(=CC=C1)S(=O)(=O)C=1C(OC2=CC=CC(=C2C=1)C(F)(F)F)=O AQWSFUIGRSMCST-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 229910052744 lithium Inorganic materials 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003863 metallic catalyst Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 2
- SHWZFQPXYGHRKT-FDGPNNRMSA-N (z)-4-hydroxypent-3-en-2-one;nickel Chemical compound [Ni].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O SHWZFQPXYGHRKT-FDGPNNRMSA-N 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- UVPKUTPZWFHAHY-UHFFFAOYSA-L 2-ethylhexanoate;nickel(2+) Chemical compound [Ni+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O UVPKUTPZWFHAHY-UHFFFAOYSA-L 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- UIEKYBOPAVTZKW-UHFFFAOYSA-L naphthalene-2-carboxylate;nickel(2+) Chemical compound [Ni+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 UIEKYBOPAVTZKW-UHFFFAOYSA-L 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
-
- 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/02—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
- C08F297/04—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising vinyl aromatic monomers and conjugated dienes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
- C08L53/025—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes modified
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J153/02—Vinyl aromatic monomers and conjugated dienes
- C09J153/025—Vinyl aromatic monomers and conjugated dienes modified
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT8822732A IT1227927B (it) | 1988-11-25 | 1988-11-25 | Copolimeri lineari a blocchi alternati. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3938927A1 DE3938927A1 (de) | 1990-05-31 |
| DE3938927C2 true DE3938927C2 (en, 2012) | 1993-02-18 |
Family
ID=11199794
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE3938927A Granted DE3938927A1 (de) | 1988-11-25 | 1989-11-24 | Lineare, alternierende-blockcopolymere |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5164455A (en, 2012) |
| CN (1) | CN1022108C (en, 2012) |
| BE (1) | BE1003077A3 (en, 2012) |
| BR (1) | BR8906186A (en, 2012) |
| CA (1) | CA2003057A1 (en, 2012) |
| DE (1) | DE3938927A1 (en, 2012) |
| DK (1) | DK592089A (en, 2012) |
| ES (1) | ES2029153A6 (en, 2012) |
| FI (1) | FI895598A7 (en, 2012) |
| FR (1) | FR2639641B1 (en, 2012) |
| GB (1) | GB2225330B (en, 2012) |
| IT (1) | IT1227927B (en, 2012) |
| MX (1) | MX169894B (en, 2012) |
| NL (1) | NL194003C (en, 2012) |
| NO (1) | NO894624L (en, 2012) |
| SE (1) | SE501518C2 (en, 2012) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1246410B (it) * | 1990-07-25 | 1994-11-18 | Enichem Elastomers | Copolimero a blocchi ramificato, procedimenti per la sua preparazione e suo impiego |
| IT1246287B (it) | 1990-07-25 | 1994-11-17 | Enichem Elastomers | Copolimero a blocchi ramificato e idrogenato e procedimenti per la sua preparazione |
| IT1244550B (it) * | 1991-02-06 | 1994-07-15 | Enichem Elastomers | Copolimeri a blocchi idrogenati contenenti gruppi epossidici e loro metodo di preparazione |
| US5310490A (en) * | 1991-03-13 | 1994-05-10 | Exxon Chemical Products Inc. | Viscosity modifer polymers |
| US5589542A (en) * | 1993-11-03 | 1996-12-31 | Shell Oil Company | Multiblock hydrogenated polymers for adhesives |
| US5718752A (en) * | 1995-10-24 | 1998-02-17 | Shell Oil Company | Asphalt composition with improved processability |
| IT1302040B1 (it) * | 1998-09-04 | 2000-07-20 | Enichem Spa | Copolimeri a blocchi idrogenati aventi struttura parzialmenteramificata. |
| WO2001044315A1 (en) * | 1999-12-15 | 2001-06-21 | Dow Global Technologies Inc. | Multi-component articles prepared from hydrogenated block copolymers |
| WO2002048211A2 (en) * | 2000-12-13 | 2002-06-20 | Dow Global Technologies Inc. | Hydrogenated block copolymers having varying sizes of hydrogenated vinyl aromatic blocks |
| US20040014877A1 (en) * | 2002-07-19 | 2004-01-22 | Null Volker Klaus | White oil as plasticizer in a polystyrene composition and process to prepare said oil |
| CN100532415C (zh) * | 2005-04-06 | 2009-08-26 | 中国科学院化学研究所 | 一种聚丙烯嵌段共聚物及其制备方法与应用 |
| CN101179933A (zh) * | 2005-05-20 | 2008-05-14 | 国际壳牌研究有限公司 | 包含费-托衍生白油作为载体油的组合物 |
| US20090171009A1 (en) * | 2005-05-20 | 2009-07-02 | Volker Klaus Null | Polysterene composition comprising a fischer tropsch derived white oil |
| ITMI20060286A1 (it) * | 2006-02-16 | 2007-08-17 | Polimeri Europa Spa | Copolimeri etilene-propilene adatti alla modifica degli oli lubrificanti e procedimento per la loro preparazione |
| KR20200042905A (ko) * | 2017-08-30 | 2020-04-24 | 니폰 제온 가부시키가이샤 | 비수계 이차 전지 전극용 바인더 조성물, 비수계 이차 전지 전극용 슬러리 조성물, 비수계 이차 전지용 전극, 및 비수계 이차 전지 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3431323A (en) * | 1964-01-20 | 1969-03-04 | Shell Oil Co | Hydrogenated block copolymers of butadiene and a monovinyl aryl hydrocarbon |
| US4153647A (en) * | 1977-06-15 | 1979-05-08 | Glukhovskoi Vladimir S | Process for producing-impact polystyrene |
| US4168286A (en) * | 1977-09-23 | 1979-09-18 | Phillips Petroleum Co. | Tetrablock polymers and their hydrogenated analogs |
| US4172826A (en) * | 1977-11-28 | 1979-10-30 | General Electric Company | Polyphenylene ether resin compositions containing EPDM rubber-modified alkenyl aromatic resins and hydrogenated elastomeric block copolymers |
| IT1186752B (it) * | 1985-07-10 | 1987-12-16 | Eniricerche Spa | Copolimeri a blocchi idrogenati e loro processo di sintesi |
| LU86698A1 (fr) * | 1986-12-04 | 1988-07-14 | Labofina Sa | Procede pour fabriquer des copolymeres blocs transparents |
| IT1222429B (it) * | 1987-07-31 | 1990-09-05 | Enichem Elastromeri S P A | Copolimero a blocchi procedimento per la sua preparazione |
-
1988
- 1988-11-25 IT IT8822732A patent/IT1227927B/it active
-
1989
- 1989-11-14 SE SE8903825A patent/SE501518C2/sv unknown
- 1989-11-15 CA CA002003057A patent/CA2003057A1/en not_active Abandoned
- 1989-11-16 GB GB8925890A patent/GB2225330B/en not_active Expired - Fee Related
- 1989-11-21 NO NO89894624A patent/NO894624L/no unknown
- 1989-11-22 FR FR898915347A patent/FR2639641B1/fr not_active Expired - Lifetime
- 1989-11-22 NL NL8902892A patent/NL194003C/nl not_active IP Right Cessation
- 1989-11-23 FI FI895598A patent/FI895598A7/fi not_active Application Discontinuation
- 1989-11-24 BR BR898906186A patent/BR8906186A/pt not_active IP Right Cessation
- 1989-11-24 DE DE3938927A patent/DE3938927A1/de active Granted
- 1989-11-24 ES ES8904406A patent/ES2029153A6/es not_active Expired - Fee Related
- 1989-11-24 BE BE8901260A patent/BE1003077A3/fr not_active IP Right Cessation
- 1989-11-24 DK DK592089A patent/DK592089A/da not_active Application Discontinuation
- 1989-11-25 CN CN89108809A patent/CN1022108C/zh not_active Expired - Lifetime
- 1989-11-27 MX MX018501A patent/MX169894B/es unknown
-
1991
- 1991-10-21 US US07/780,126 patent/US5164455A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB8925890D0 (en) | 1990-01-04 |
| FR2639641B1 (fr) | 1993-08-06 |
| BR8906186A (pt) | 1990-06-26 |
| BE1003077A3 (fr) | 1991-11-12 |
| SE501518C2 (sv) | 1995-03-06 |
| GB2225330A (en) | 1990-05-30 |
| SE8903825D0 (sv) | 1989-11-14 |
| NO894624L (no) | 1990-05-28 |
| CN1044107A (zh) | 1990-07-25 |
| MX169894B (es) | 1993-07-29 |
| FI895598A0 (fi) | 1989-11-23 |
| NL8902892A (nl) | 1990-06-18 |
| FR2639641A1 (fr) | 1990-06-01 |
| NO894624D0 (no) | 1989-11-21 |
| GB2225330B (en) | 1992-07-15 |
| CA2003057A1 (en) | 1990-05-25 |
| DK592089D0 (da) | 1989-11-24 |
| IT8822732A0 (it) | 1988-11-25 |
| IT1227927B (it) | 1991-05-14 |
| CN1022108C (zh) | 1993-09-15 |
| NL194003B (nl) | 2000-12-01 |
| SE8903825L (sv) | 1990-05-26 |
| FI895598A7 (fi) | 1990-05-26 |
| US5164455A (en) | 1992-11-17 |
| DK592089A (da) | 1990-05-26 |
| DE3938927A1 (de) | 1990-05-31 |
| ES2029153A6 (es) | 1992-07-16 |
| NL194003C (nl) | 2001-04-03 |
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