ITSA990005A1 - Copolimeri a base di propilene contenenti unita' stireniche - Google Patents
Copolimeri a base di propilene contenenti unita' stirenicheInfo
- Publication number
- ITSA990005A1 ITSA990005A1 IT1999SA000005A ITSA990005A ITSA990005A1 IT SA990005 A1 ITSA990005 A1 IT SA990005A1 IT 1999SA000005 A IT1999SA000005 A IT 1999SA000005A IT SA990005 A ITSA990005 A IT SA990005A IT SA990005 A1 ITSA990005 A1 IT SA990005A1
- Authority
- IT
- Italy
- Prior art keywords
- atom
- copolymers
- propylene
- units
- styrene
- Prior art date
Links
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 title claims description 35
- 229920001577 copolymer Polymers 0.000 title claims description 20
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 22
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 16
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 15
- 239000005977 Ethylene Substances 0.000 claims description 15
- 238000006116 polymerization reaction Methods 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 150000003440 styrenes Chemical class 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 238000003780 insertion Methods 0.000 claims description 3
- 230000037431 insertion Effects 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 125000004437 phosphorous atom Chemical group 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000002685 polymerization catalyst Substances 0.000 claims description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 8
- -1 polypropylene Polymers 0.000 description 8
- 239000004743 Polypropylene Substances 0.000 description 7
- 229920001155 polypropylene Polymers 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 230000003197 catalytic effect Effects 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 4
- 238000000113 differential scanning calorimetry Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920006301 statistical copolymer Polymers 0.000 description 4
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000002638 heterogeneous catalyst Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910007928 ZrCl2 Inorganic materials 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229920001580 isotactic polymer Polymers 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 239000012815 thermoplastic material Substances 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
-
- 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- 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
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/12—Monomers containing a branched unsaturated aliphatic radical or a ring substituted by an alkyl radical
-
- 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
- C08F218/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F218/02—Esters of monocarboxylic acids
- C08F218/04—Vinyl esters
- C08F218/08—Vinyl acetate
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
- C08F220/44—Acrylonitrile
-
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT1999SA000005A ITSA990005A1 (it) | 1999-02-11 | 1999-02-11 | Copolimeri a base di propilene contenenti unita' stireniche |
| EP00910679A EP1071720A1 (en) | 1999-02-11 | 2000-02-10 | Propylene copolymers containing styrene units |
| AU32807/00A AU3280700A (en) | 1999-02-11 | 2000-02-10 | Propylene copolymers containing styrene units |
| PCT/EP2000/001219 WO2000047643A1 (en) | 1999-02-11 | 2000-02-10 | Propylene copolymers containing styrene units |
| BR0004772-4A BR0004772A (pt) | 1999-02-11 | 2000-02-10 | Copolìmeros de propileno contendo unidades de estireno. |
| CA002327781A CA2327781A1 (en) | 1999-02-11 | 2000-02-10 | Propylene copolymers containing styrene units |
| CN00800512A CN1300300A (zh) | 1999-02-11 | 2000-02-10 | 含有苯乙烯单元的丙烯共聚物 |
| KR1020007011224A KR20010042561A (ko) | 1999-02-11 | 2000-02-10 | 스티렌 단위를 함유하는 프로필렌 공중합체 |
| JP2000598558A JP2002536514A (ja) | 1999-02-11 | 2000-02-10 | スチレン単位を含むプロピレンコポリマー |
| NO20005101A NO20005101L (no) | 1999-02-11 | 2000-10-10 | Propylenkopolymerer inneholdende styren-enheter |
| US10/068,361 US6617410B2 (en) | 1999-02-11 | 2002-02-06 | Propylene copolymers containing styrene units |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT1999SA000005A ITSA990005A1 (it) | 1999-02-11 | 1999-02-11 | Copolimeri a base di propilene contenenti unita' stireniche |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ITSA990005A1 true ITSA990005A1 (it) | 2000-08-11 |
Family
ID=11407640
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IT1999SA000005A ITSA990005A1 (it) | 1999-02-11 | 1999-02-11 | Copolimeri a base di propilene contenenti unita' stireniche |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1071720A1 (ko) |
| JP (1) | JP2002536514A (ko) |
| KR (1) | KR20010042561A (ko) |
| CN (1) | CN1300300A (ko) |
| AU (1) | AU3280700A (ko) |
| BR (1) | BR0004772A (ko) |
| CA (1) | CA2327781A1 (ko) |
| IT (1) | ITSA990005A1 (ko) |
| NO (1) | NO20005101L (ko) |
| WO (1) | WO2000047643A1 (ko) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002102863A1 (en) * | 2001-06-15 | 2002-12-27 | Dow Global Technologies Inc. | Alpha-olefin based branched polymer |
| FR2828198B1 (fr) | 2001-07-31 | 2007-02-23 | Atofina | Polypropylene isotactique obtenu par catalyse metallocene greffe |
| EP1866348B1 (en) | 2005-04-02 | 2011-08-24 | LG Chem. Ltd. | Method of producing styren polymers using high speed catalytic dispersion technology |
| CA2944986C (en) * | 2014-04-18 | 2022-02-22 | Nippon A&L Inc. | Graft copolymer and thermoplastic resin composition |
| CN116176018B (zh) * | 2023-02-23 | 2023-11-14 | 河北海伟电子新材料科技股份有限公司 | 一种应用于电子防监标签的聚丙烯电容薄膜及其制备方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2927566B2 (ja) * | 1991-03-28 | 1999-07-28 | 出光興産株式会社 | スチレン系共重合体の製造方法 |
| US5543484A (en) * | 1994-11-18 | 1996-08-06 | The Penn State Research Foundation | α-olefin/para-alkylstyrene copolymers |
| EP0718323A3 (en) * | 1994-12-19 | 1998-01-14 | Sumitomo Chemical Company Limited | Ethylene type quaternary copolymer rubber |
| JP3489697B2 (ja) * | 1995-04-04 | 2004-01-26 | 電気化学工業株式会社 | プロピレン−芳香族ビニル化合物共重合体及びその製造方法 |
| DE19711339B4 (de) * | 1996-03-19 | 2008-09-11 | Denki Kagaku Kogyo K.K. | Copolymer aus Ethylen und aromatischer Vinylverbindung, Verfahren zu dessen Herstellung, Formkörper daraus sowie Zusammensetzung umfassend das Copolymer |
| TW473503B (en) * | 1996-09-04 | 2002-01-21 | Dow Chemical Co | Substantially random interpolymer comprising Α-olefin/vinyl aromatic monomer and/or hindered aliphatic or cycloaliphatic vinyl or vinylidene monomers, ethylene/styrene copolymer, and process for preparing Α-olefin/vinyl aromatic monomer interpoly |
| EP0872492B1 (en) * | 1997-04-17 | 2003-12-03 | Denki Kagaku Kogyo Kabushiki Kaisha | Transition metal compound as catalyst component for polymerization, aromatic vinyl compound-olefin copolymer having stereoregularity and method for its preparation by means of the transition metal compound as catalyst component |
-
1999
- 1999-02-11 IT IT1999SA000005A patent/ITSA990005A1/it unknown
-
2000
- 2000-02-10 BR BR0004772-4A patent/BR0004772A/pt not_active IP Right Cessation
- 2000-02-10 AU AU32807/00A patent/AU3280700A/en not_active Abandoned
- 2000-02-10 CA CA002327781A patent/CA2327781A1/en not_active Abandoned
- 2000-02-10 CN CN00800512A patent/CN1300300A/zh active Pending
- 2000-02-10 EP EP00910679A patent/EP1071720A1/en not_active Withdrawn
- 2000-02-10 JP JP2000598558A patent/JP2002536514A/ja active Pending
- 2000-02-10 WO PCT/EP2000/001219 patent/WO2000047643A1/en not_active Application Discontinuation
- 2000-02-10 KR KR1020007011224A patent/KR20010042561A/ko not_active Application Discontinuation
- 2000-10-10 NO NO20005101A patent/NO20005101L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2000047643A1 (en) | 2000-08-17 |
| AU3280700A (en) | 2000-08-29 |
| NO20005101L (no) | 2000-11-09 |
| BR0004772A (pt) | 2000-11-21 |
| NO20005101D0 (no) | 2000-10-10 |
| CA2327781A1 (en) | 2000-08-17 |
| KR20010042561A (ko) | 2001-05-25 |
| EP1071720A1 (en) | 2001-01-31 |
| CN1300300A (zh) | 2001-06-20 |
| JP2002536514A (ja) | 2002-10-29 |
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