DE102009027446A1 - Modifizierte Polyolefine mit besonderem Eigenschaftsprofil, Verfahren zu deren Herstellung und deren Verwendung - Google Patents
Modifizierte Polyolefine mit besonderem Eigenschaftsprofil, Verfahren zu deren Herstellung und deren Verwendung Download PDFInfo
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- DE102009027446A1 DE102009027446A1 DE102009027446A DE102009027446A DE102009027446A1 DE 102009027446 A1 DE102009027446 A1 DE 102009027446A1 DE 102009027446 A DE102009027446 A DE 102009027446A DE 102009027446 A DE102009027446 A DE 102009027446A DE 102009027446 A1 DE102009027446 A1 DE 102009027446A1
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- mass
- polymers
- butene
- polyolefins
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- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- GJIDOLBZYSCZRX-UHFFFAOYSA-N hydroxymethyl prop-2-enoate Chemical compound OCOC(=O)C=C GJIDOLBZYSCZRX-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
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- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
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- 239000002650 laminated plastic Substances 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 239000013627 low molecular weight specie Substances 0.000 description 1
- 230000005389 magnetism Effects 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000003446 memory effect Effects 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- 229920006113 non-polar polymer Polymers 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010943 off-gassing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 230000003534 oscillatory effect Effects 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
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- 230000008092 positive effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 239000010453 quartz Substances 0.000 description 1
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- 238000007086 side reaction Methods 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
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- 229910002027 silica gel Inorganic materials 0.000 description 1
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- 238000007711 solidification Methods 0.000 description 1
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- 125000006850 spacer group Chemical group 0.000 description 1
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- 238000007655 standard test method Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test 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
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000005028 tinplate Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 239000003190 viscoelastic substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
- C08F230/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
- C08F230/08—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
- C08F230/085—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon the monomer being a polymerisable silane, e.g. (meth)acryloyloxy trialkoxy silanes or vinyl trialkoxysilanes
-
- 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
-
- 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
- C08F255/08—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having four or more carbon atoms
- C08F255/10—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having four or more carbon atoms on to butene polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/06—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- 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
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/06—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009027446A DE102009027446A1 (de) | 2009-07-03 | 2009-07-03 | Modifizierte Polyolefine mit besonderem Eigenschaftsprofil, Verfahren zu deren Herstellung und deren Verwendung |
| EP10167292A EP2277931B1 (de) | 2009-07-03 | 2010-06-25 | Modifizierte Polyolefine mit besonderem Eigenschaftsprofil, Verfahren zu deren Herstellung und deren Verwendung |
| AT10167292T ATE550362T1 (de) | 2009-07-03 | 2010-06-25 | Modifizierte polyolefine mit besonderem eigenschaftsprofil, verfahren zu deren herstellung und deren verwendung |
| JP2010152948A JP5599241B2 (ja) | 2009-07-03 | 2010-07-05 | 極めて優れた特性のプロファイルを有する変性ポリオレフィン、それらの製造方法およびそれらの使用 |
| US12/830,869 US8530582B2 (en) | 2009-07-03 | 2010-07-06 | Modified polyolefins with an exceptional profile of properties, process for preparation thereof and use thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009027446A DE102009027446A1 (de) | 2009-07-03 | 2009-07-03 | Modifizierte Polyolefine mit besonderem Eigenschaftsprofil, Verfahren zu deren Herstellung und deren Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102009027446A1 true DE102009027446A1 (de) | 2011-01-05 |
Family
ID=42561161
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102009027446A Withdrawn DE102009027446A1 (de) | 2009-07-03 | 2009-07-03 | Modifizierte Polyolefine mit besonderem Eigenschaftsprofil, Verfahren zu deren Herstellung und deren Verwendung |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8530582B2 (https=) |
| EP (1) | EP2277931B1 (https=) |
| JP (1) | JP5599241B2 (https=) |
| AT (1) | ATE550362T1 (https=) |
| DE (1) | DE102009027446A1 (https=) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US9115272B2 (en) | 2007-09-20 | 2015-08-25 | Adco Products Llc | Edge sealants having balanced properties |
| DE102008005949A1 (de) * | 2008-01-24 | 2009-07-30 | Evonik Degussa Gmbh | Polyolefine mit Isotaktischen Strukturelementen, Verfahren zu deren Herstellung und deren Verwendung |
| CN102742005B (zh) * | 2009-10-14 | 2016-04-20 | 阿德科产品有限责任公司 | 具有平衡的性质的边缘密封剂 |
| EP2552673B1 (en) * | 2010-03-30 | 2014-01-08 | NV Bekaert SA | A splice for jointing steel cord strips encased in thermoplastic material |
| SG11201505126PA (en) * | 2012-12-31 | 2015-07-30 | Dow Global Technologies Llc | Pressure sensitive adhesive composition with silane grafted olefin block copolymer |
| MX386556B (es) | 2013-09-18 | 2025-03-19 | Holcim Technology Ltd | Membranas para techo que se pegan y despegan con adhesivos curados sensibles a la presión. |
| US10696765B2 (en) | 2014-02-07 | 2020-06-30 | Eastman Chemical Company | Adhesive composition comprising amorphous propylene-ethylene copolymer and propylene polymer |
| US11267916B2 (en) | 2014-02-07 | 2022-03-08 | Eastman Chemical Company | Adhesive composition comprising amorphous propylene-ethylene copolymer and polyolefins |
| US10723824B2 (en) | 2014-02-07 | 2020-07-28 | Eastman Chemical Company | Adhesives comprising amorphous propylene-ethylene copolymers |
| US10308740B2 (en) | 2014-02-07 | 2019-06-04 | Eastman Chemical Company | Amorphous propylene-ethylene copolymers |
| US9428598B2 (en) | 2014-02-07 | 2016-08-30 | Eastman Chemical Company | Amorphous propylene-ethylene copolymers |
| US10647795B2 (en) | 2014-02-07 | 2020-05-12 | Eastman Chemical Company | Adhesive composition comprising amorphous propylene-ethylene copolymer and polyolefins |
| US10065394B2 (en) | 2014-03-07 | 2018-09-04 | Firestone Building Products Co., LLC | Roofing membranes with pre-applied, cured, pressure-sensitive seam adhesives |
| RU2568736C1 (ru) * | 2014-06-03 | 2015-11-20 | Открытое акционерное общество "Композит" (ОАО "Композит") | Композиция для эластичного теплопроводного клея |
| JP6591244B2 (ja) * | 2015-09-18 | 2019-10-16 | 出光興産株式会社 | タイヤ用ゴム組成物 |
| US10361423B2 (en) * | 2016-01-18 | 2019-07-23 | Grst International Limited | Method of preparing battery electrodes |
| WO2017165870A1 (en) | 2016-03-25 | 2017-09-28 | Firestone Building Products Co., LLC | Fabric-backed roofing membrane composite |
| US12006692B2 (en) | 2016-03-25 | 2024-06-11 | Holcim Technology Ltd | Fully-adhered roof system adhered and seamed with a common adhesive |
| WO2017165871A1 (en) | 2016-03-25 | 2017-09-28 | Firestone Building Products Co., LLC | Method of reroofing |
| US20200299965A1 (en) | 2016-03-25 | 2020-09-24 | Firestone Building Products Company, Llc | Fully-adhered roof system adhered and seamed with a common adhesive |
| EP3348589B1 (de) | 2017-01-16 | 2019-08-07 | Evonik Degussa GmbH | Polybutadiene, deren herstellung und verwendung |
| DE102019204773B4 (de) | 2019-04-03 | 2023-02-09 | IGK Isolierglasklebstoffe GmbH | System zur Herstellung eines Dichtmassenverbunds für Isolierglas, dessen Verwendung, Randverbund zur Herstellung von Isolierglas oder Solarmodulen und Isolierglaseinheit |
| EP3808809A1 (de) | 2019-10-16 | 2021-04-21 | Evonik Operations GmbH | Amorphes poly-alpha-olefin enthaltendes polyolefingemenge |
| IT202000001660A1 (it) * | 2020-01-29 | 2021-07-29 | Savare I C S R L | Adesivi termofusibili con migliorata adesione e coesione |
| WO2022013055A1 (en) * | 2020-07-13 | 2022-01-20 | Borealis Ag | Adhesive polyethylene composition |
| WO2022244879A1 (ja) * | 2021-05-20 | 2022-11-24 | 三井化学株式会社 | 樹脂組成物及びその用途ならびに製造方法 |
| WO2023081010A1 (en) | 2021-11-05 | 2023-05-11 | Exxonmobil Chemical Patents Inc. | Polypropylene viscosity modifiers and lubricating oils thereof |
| CN115975550B (zh) * | 2023-02-14 | 2023-06-20 | 宁德新能源科技有限公司 | 粘结剂组合物、电化学装置及用电装置 |
| CN116956143A (zh) * | 2023-06-12 | 2023-10-27 | 深圳大学 | 光谱数据的模型构建及分类检测方法、装置、设备及介质 |
Citations (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3075948A (en) | 1959-10-23 | 1963-01-29 | Owens Illinois Glass Co | Method for preparing graft copolymers of polyolefin and silanes and a graft copolymer thereof |
| DE1963571A1 (de) | 1968-12-20 | 1970-10-29 | Midland Siliconas Ltd | Verfahren zur Vernetzung von Polyolefinen |
| DE2353783A1 (de) | 1972-10-28 | 1974-05-09 | Dow Corning Ltd | Verfahren zur vernetzung von polyolefinen |
| DE2406844A1 (de) | 1973-02-14 | 1974-08-22 | Dow Corning Ltd | Verfahren zum vernetzen von polyolefinen |
| DE2554525A1 (de) | 1974-12-06 | 1976-06-16 | Bicc Ltd | Verfahren zur herstellung von stranggepressten produkten |
| DE2642927A1 (de) | 1975-09-26 | 1977-03-31 | Bicc Ltd | Verfahren zur herstellung von stranggepressten produkten |
| EP0004034A1 (en) | 1978-03-03 | 1979-09-19 | The Furukawa Electric Co., Ltd. | Method of crosslinking poly-alpha-olefin series resins |
| EP0260103A1 (en) | 1986-09-10 | 1988-03-16 | UNIROYAL CHEMICAL COMPANY, Inc. | Moisture-curable low molecular weight polymers and compositions and composites thereof |
| WO1989011513A1 (en) | 1988-05-17 | 1989-11-30 | Swift Adhesives Limited | Adhesive compositions |
| EP0384264A1 (de) | 1989-02-15 | 1990-08-29 | Hoechst Aktiengesellschaft | Polypropylenwachs und Verfahren zu seiner Herstellung |
| WO1991006580A1 (en) | 1989-11-01 | 1991-05-16 | Swift Adhesives Limited | Crosslinkable polymers |
| DE4000695A1 (de) | 1990-01-12 | 1991-07-18 | Huels Chemische Werke Ag | Verfahren zur herstellung weitgehend amorpher polyalphaolefine mit enger molekulargewichtsverteilung |
| EP0480390A2 (de) | 1990-10-11 | 1992-04-15 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung eines Polyolefins |
| EP0516018A2 (de) | 1991-05-27 | 1992-12-02 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Polyolefinen mit breiter Molmassenverteilung |
| EP0584609A2 (de) | 1992-08-15 | 1994-03-02 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Polyolefinen |
| DE19516457A1 (de) | 1994-05-04 | 1995-11-09 | Du Pont Canada | Vernetzbare Klebstoff-Polymere |
| EP0827994A2 (de) | 1996-09-04 | 1998-03-11 | Hüls Aktiengesellschaft | Verwendung von silangepfropften amorphen Poly-alpha-Olefinen als feuchtigkeitsvernetzender Klebrohstoff oder Klebstoff |
| WO2000037514A1 (en) | 1998-12-21 | 2000-06-29 | Exxon Chemical Patents Inc. | Branched semi-crystalline ethylene-propylene compositions |
| US6121377A (en) | 1998-09-10 | 2000-09-19 | Academy Of Applied Science | Process for the production of thermoplastic elastomeric polyolefin alloys, including syndiotactic-atactic polypropylene alloys and isotactic-atactic polypropylene alloys, and catalysts therefore |
| WO2001046278A2 (en) | 1999-12-21 | 2001-06-28 | Exxon Chemical Patents Inc. | Adhesive alpha-olefin inter-polymers |
| WO2001046274A1 (de) | 1999-12-21 | 2001-06-28 | Basell Polyolefine Gmbh | Teilkristalline propylenpolymerisat-zusammensetzung zur herstellung von biaxial gereckten polypropylenfolien |
| JP2003002930A (ja) | 2000-05-08 | 2003-01-08 | Sumitomo Chem Co Ltd | 非晶性オレフィン系重合体変性物、ならびに、該変性物と熱可塑性樹脂を含有する樹脂組成物 |
| WO2003070786A1 (en) | 2002-02-20 | 2003-08-28 | Idemitsu Petrochemical Co., Ltd. | Process for producing modified butene-1 polymer and modified butene-1 polymer obtained by the process |
| US20040110910A1 (en) | 2002-12-05 | 2004-06-10 | Palanisamy Arjunan | High temperature bulk polymerization of branched crystalline polypropylene |
| JP2004196848A (ja) | 2002-12-16 | 2004-07-15 | Idemitsu Petrochem Co Ltd | ブテン系ブロック共重合体及びその製造方法 |
| EP1508579A1 (de) | 2003-08-21 | 2005-02-23 | Clariant GmbH | Modifizierte Polyolefinwachse |
| WO2006069205A1 (en) | 2004-12-21 | 2006-06-29 | Dow Global Technologies Inc. | Polypropylene-based adhesive compositions |
| WO2007002177A1 (en) | 2005-06-24 | 2007-01-04 | Exxonmobil Chemical Patents Inc. | Plasticized functionalized propylene copolymer adhesive composition |
| WO2007001694A1 (en) | 2005-06-24 | 2007-01-04 | Exxonmobil Chemical Patents Inc. | Functionalized propylene copolymer adheside composition |
| WO2007008765A2 (en) | 2005-07-11 | 2007-01-18 | Dow Global Technologies Inc. | Silane-grafted olefin polymers, compositions and articles prepared therefrom, and methods for making the same |
| WO2007067243A1 (en) | 2005-12-07 | 2007-06-14 | Exxonmobil Chemical Patents Inc. | Method for the functional i zation of polypropylene materials |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69300609T2 (de) * | 1992-04-01 | 1996-06-13 | Mitsui Toatsu Chemicals | Syndiotaktischen Polypropylen, Wachs, Verfahren zur Herstellung derselbe und ihre Anwendung in eine Wärmefixiertonerzusammensetzung für geheizte Walze. |
| EP1377614A2 (en) * | 2000-12-12 | 2004-01-07 | Baker Hughes Incorporated | Low molecular weight isotactic polypropylene polymers, copolymers and derivatives and materials prepared therewith |
| DE10114345A1 (de) * | 2001-03-23 | 2002-09-26 | Bayer Ag | Katalysator mit einer Donor-Akzeptor-Wechselwirkung |
| DE10228622A1 (de) | 2002-06-26 | 2004-01-15 | Degussa Ag | Verfahren zur Noppen- und Filamenteinbindung von Teppichrohwaren |
| TWI296270B (en) * | 2002-07-19 | 2008-05-01 | Mitsui Chemicals Inc | Propylene copolymer, polypropylene composition and its usage, and transition metal compound, catalyst for olefinic polymerization |
| US7807768B2 (en) | 2005-04-13 | 2010-10-05 | Evonik Degussa Gmbh | Highly viscous, largely amorphous polyolefin |
| DE102005017200A1 (de) | 2005-04-13 | 2006-10-19 | Degussa Ag | Verwendung eines hochviskosen, weitgehend amorphen Polyolefins zur Herstellung einer Folie |
| DE102005026765A1 (de) | 2005-06-10 | 2006-12-14 | Degussa Ag | Rückenfixierung von Kunstrasenrohware mit Schmelzklebern auf Basis von amorphen Poly-alpha-Olefinen und/oder modifizierten, amorphen Poly-alpha-Olefinen |
| DE102008005947A1 (de) | 2008-01-24 | 2009-07-30 | Evonik Degussa Gmbh | Polyolefine mit Ataktischen Strukturelementen, Verfahren zu deren Herstellung und deren Verwendung |
| DE102008005949A1 (de) * | 2008-01-24 | 2009-07-30 | Evonik Degussa Gmbh | Polyolefine mit Isotaktischen Strukturelementen, Verfahren zu deren Herstellung und deren Verwendung |
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Patent Citations (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3075948A (en) | 1959-10-23 | 1963-01-29 | Owens Illinois Glass Co | Method for preparing graft copolymers of polyolefin and silanes and a graft copolymer thereof |
| DE1963571A1 (de) | 1968-12-20 | 1970-10-29 | Midland Siliconas Ltd | Verfahren zur Vernetzung von Polyolefinen |
| DE2353783A1 (de) | 1972-10-28 | 1974-05-09 | Dow Corning Ltd | Verfahren zur vernetzung von polyolefinen |
| DE2406844A1 (de) | 1973-02-14 | 1974-08-22 | Dow Corning Ltd | Verfahren zum vernetzen von polyolefinen |
| DE2554525A1 (de) | 1974-12-06 | 1976-06-16 | Bicc Ltd | Verfahren zur herstellung von stranggepressten produkten |
| DE2642927A1 (de) | 1975-09-26 | 1977-03-31 | Bicc Ltd | Verfahren zur herstellung von stranggepressten produkten |
| EP0004034A1 (en) | 1978-03-03 | 1979-09-19 | The Furukawa Electric Co., Ltd. | Method of crosslinking poly-alpha-olefin series resins |
| EP0260103A1 (en) | 1986-09-10 | 1988-03-16 | UNIROYAL CHEMICAL COMPANY, Inc. | Moisture-curable low molecular weight polymers and compositions and composites thereof |
| WO1989011513A1 (en) | 1988-05-17 | 1989-11-30 | Swift Adhesives Limited | Adhesive compositions |
| EP0384264A1 (de) | 1989-02-15 | 1990-08-29 | Hoechst Aktiengesellschaft | Polypropylenwachs und Verfahren zu seiner Herstellung |
| WO1991006580A1 (en) | 1989-11-01 | 1991-05-16 | Swift Adhesives Limited | Crosslinkable polymers |
| DE4000695A1 (de) | 1990-01-12 | 1991-07-18 | Huels Chemische Werke Ag | Verfahren zur herstellung weitgehend amorpher polyalphaolefine mit enger molekulargewichtsverteilung |
| EP0480390A2 (de) | 1990-10-11 | 1992-04-15 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung eines Polyolefins |
| EP0516018A2 (de) | 1991-05-27 | 1992-12-02 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Polyolefinen mit breiter Molmassenverteilung |
| EP0584609A2 (de) | 1992-08-15 | 1994-03-02 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Polyolefinen |
| DE19516457A1 (de) | 1994-05-04 | 1995-11-09 | Du Pont Canada | Vernetzbare Klebstoff-Polymere |
| EP0827994A2 (de) | 1996-09-04 | 1998-03-11 | Hüls Aktiengesellschaft | Verwendung von silangepfropften amorphen Poly-alpha-Olefinen als feuchtigkeitsvernetzender Klebrohstoff oder Klebstoff |
| US6121377A (en) | 1998-09-10 | 2000-09-19 | Academy Of Applied Science | Process for the production of thermoplastic elastomeric polyolefin alloys, including syndiotactic-atactic polypropylene alloys and isotactic-atactic polypropylene alloys, and catalysts therefore |
| WO2000037514A1 (en) | 1998-12-21 | 2000-06-29 | Exxon Chemical Patents Inc. | Branched semi-crystalline ethylene-propylene compositions |
| WO2001046278A2 (en) | 1999-12-21 | 2001-06-28 | Exxon Chemical Patents Inc. | Adhesive alpha-olefin inter-polymers |
| WO2001046274A1 (de) | 1999-12-21 | 2001-06-28 | Basell Polyolefine Gmbh | Teilkristalline propylenpolymerisat-zusammensetzung zur herstellung von biaxial gereckten polypropylenfolien |
| EP1263815A2 (en) | 1999-12-21 | 2002-12-11 | Exxon Chemical Patents Inc. | Adhesive alpha-olefin inter-polymers |
| JP2003002930A (ja) | 2000-05-08 | 2003-01-08 | Sumitomo Chem Co Ltd | 非晶性オレフィン系重合体変性物、ならびに、該変性物と熱可塑性樹脂を含有する樹脂組成物 |
| WO2003070786A1 (en) | 2002-02-20 | 2003-08-28 | Idemitsu Petrochemical Co., Ltd. | Process for producing modified butene-1 polymer and modified butene-1 polymer obtained by the process |
| US20040110910A1 (en) | 2002-12-05 | 2004-06-10 | Palanisamy Arjunan | High temperature bulk polymerization of branched crystalline polypropylene |
| JP2004196848A (ja) | 2002-12-16 | 2004-07-15 | Idemitsu Petrochem Co Ltd | ブテン系ブロック共重合体及びその製造方法 |
| EP1508579A1 (de) | 2003-08-21 | 2005-02-23 | Clariant GmbH | Modifizierte Polyolefinwachse |
| WO2006069205A1 (en) | 2004-12-21 | 2006-06-29 | Dow Global Technologies Inc. | Polypropylene-based adhesive compositions |
| WO2007002177A1 (en) | 2005-06-24 | 2007-01-04 | Exxonmobil Chemical Patents Inc. | Plasticized functionalized propylene copolymer adhesive composition |
| WO2007001694A1 (en) | 2005-06-24 | 2007-01-04 | Exxonmobil Chemical Patents Inc. | Functionalized propylene copolymer adheside composition |
| WO2007008765A2 (en) | 2005-07-11 | 2007-01-18 | Dow Global Technologies Inc. | Silane-grafted olefin polymers, compositions and articles prepared therefrom, and methods for making the same |
| WO2007067243A1 (en) | 2005-12-07 | 2007-06-14 | Exxonmobil Chemical Patents Inc. | Method for the functional i zation of polypropylene materials |
Non-Patent Citations (44)
| Title |
|---|
| [4] J. C. Randall, Polymer Sequence Determination, Academic Press, New York 1977 |
| A. E. Tonelli, NMR Spectroscopy and Polymer Microstructure, Verlag Chemie Weinheim 1989 |
| A. F. Mason, G. W. Coates in: "Macromolecular Engineering"; Wiley-VCH, Weinheim; 2007 |
| A. Filho, G. Galland: J. Appl. Polym. Sci., 80, 1880 (2001) |
| A. Lehtinen; Macromol. Chem. Phys.; 195(1994); 1539ff |
| A. Rudin, H. L. W. Hoegy; J. Polym. Sci.; A1; 10; 217 (1972) |
| A. Zambelli et al: Macromolecules, 8, 687 (1975) |
| Adv. Organomet. Chem. 1980, 18, 99-149 |
| ASTM D 4440-01 |
| ASTM D6474-99 |
| B. A. Krentsel, Y. V. Kissin, V. I. Kleiner, L. L. Stotskaya; "Polymers and Copolymers of higher 1-Olefins"; S. 19/20; Hanser Publ.; München; 1997 |
| B. Ivan, Z. Laszlo-Hedvig, T. Kelen, F. Tüdos; Polym. Bull.; 8; 311 (1982) |
| D. Goedhart, A. Opschoor; J. Polym. Sci.; A2; 8; 1227 (1970) |
| DIN 53 765 |
| DIN EN 1426 |
| DIN EN 1427 |
| DIN EN 1465 |
| DIN EN ISO 527-3 |
| G. Natta, I. Pasquon, A. Zambelli, G. Gatti; Makromol. Chem.; 70 (1964); 191ff |
| G. Samay, M. Kubin, J. Podesva; Angew. Makromol. Chem.; 72; 185 (1978) |
| H. EI Mansouri, N. Yagoubi, D. Scholler, A. Feigenbaum, D. Ferrier; J. Appl. Polym. Sci.; 71 (1999); 371ff |
| H. G. Elias: "Makromoleküle"; Bd. 2; Wiley-VCH; Weinheim 2001 |
| H.-G. Elias, Makromoleküle, Band 2, 6. Auflage, Wiley-VCH, Weinheim 2001, S. 411-413 |
| H.-G. Elias; Makromoleküle; Bd. III; Wiley-VCH: Weinheim; 2001 |
| J. Bicerano; J. M. S.; Rev. Macromol. Chem. Phys.; C38 (1998); 391ff |
| J. Boor; "Ziegler-Natta Catalysts and Polymerization"; Academic Press; New York; 1979 |
| J. L. Koenig, Spectroscopy of Polymers, ACS Professional Reference Books, Washington 1992 |
| J. Meissner; "Rheologisches Verhalten von Kunststoff-Schmelzen und -Lösungen" in: "Praktische Rheologie der Kunststoffe"; VD/-Verlag; Düsseldorf; 1978 |
| J.-F. Jansson; Proc. 8th. Int. Congr. Rheol.; 1980; Vol. 3 |
| K. A. Boni, F. A. Sliemers, P. B. Stickney; J. Polym. Sci.; A2; 6; 1579 (1968) |
| K.-Q. Wang, S.-Y. Zhang, J. Xu, Y. Li, H. P. Li; J. Liqu. Chrom.; 5; 1899 (1982) |
| Kaminsky et al. |
| L. Resconi in: "Metallocene based Polyolefins"; J. Scheirs, W. Kaminsky (Hrsg.); J. Wiley & Sons; Weinheim; 1999 |
| N. P. Cheremisinoff; "An Introduction to Polymer Rheology and Processing"; CRC Press; London; 1993 |
| R. S. Lenk; "Rheologie der Kunststoffe"; C. Hanser Verlag; München; 1971 |
| R. Vieweg, A. Schley, A. Schwarz (Hrsg); Kunststoff Handbuch; Bd. IV/"Polyolefine"; C. Hanser Verlag, München 1969 |
| S. Berger, S. Braun, H.-O. Kalinowski, 13C-NMR-Spektroskopie, Georg Thieme Verlag Stuttgart 1985 |
| S. Davison, G. L. Taylor; Br. Polym. J.; 4 (1972); 65ff |
| T. G. Scholte, H. M. Schoffeleers, A. M. G. Brands; J. Appl. Polym. Sci.; 29; 3763 (1984) |
| T. Shiomura, N. Uchikawa, T. Asanuma, R. Sugimoto, I. Fujio, S. Kimura, S. Harima, M. Akiyama, M. Kohno, N. Inoue in: "Metallocene based Polyolefins"; J. Scheirs, W. Kaminsky (Hrsg.); J. Wiley & Sons; Weinheim; 1999 |
| W. Spaleck in: "Metallocene based Polyolefins"; J. Scheirs, W. Kaminsky (Hrsg.); J. Wiley & Sons; Weinheim; 1999 |
| Walter, Philipp; Mader, Dietmar; Reichert, Peter; Mulhaupt, Rolf; Journal of Macromolecular Science, Pure and Applied Chemistry (1999), A36(11), 1613-1639 |
| Y. V. Kissin; "Isospecific polymerization of olefins"; Springer Verlag; New York; 1985 |
| Z. Grubisic, P. Rempp, H. Benoit; Polym. Lett.; 5; 753 (1967) |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5599241B2 (ja) | 2014-10-01 |
| EP2277931B1 (de) | 2012-03-21 |
| JP2011012261A (ja) | 2011-01-20 |
| EP2277931A1 (de) | 2011-01-26 |
| US8530582B2 (en) | 2013-09-10 |
| US20110003916A1 (en) | 2011-01-06 |
| ATE550362T1 (de) | 2012-04-15 |
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