MX2008011718A - Interpolimeros de bloques de propileno/alfa-olefina. - Google Patents
Interpolimeros de bloques de propileno/alfa-olefina.Info
- Publication number
- MX2008011718A MX2008011718A MX2008011718A MX2008011718A MX2008011718A MX 2008011718 A MX2008011718 A MX 2008011718A MX 2008011718 A MX2008011718 A MX 2008011718A MX 2008011718 A MX2008011718 A MX 2008011718A MX 2008011718 A MX2008011718 A MX 2008011718A
- Authority
- MX
- Mexico
- Prior art keywords
- propylene
- olefin
- interpolymer
- olefin interpolymer
- fraction
- Prior art date
Links
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 title claims abstract description 188
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 title claims abstract description 186
- 239000004711 α-olefin Substances 0.000 title claims description 123
- 238000009826 distribution Methods 0.000 claims abstract description 38
- 238000010828 elution Methods 0.000 claims abstract description 23
- 238000005194 fractionation Methods 0.000 claims abstract description 10
- 229920000642 polymer Polymers 0.000 claims description 167
- -1 1-ketene Chemical compound 0.000 claims description 42
- 238000002844 melting Methods 0.000 claims description 23
- 230000008018 melting Effects 0.000 claims description 23
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 19
- 239000005977 Ethylene Substances 0.000 claims description 18
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 17
- 229920000098 polyolefin Polymers 0.000 claims description 15
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 14
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 11
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 claims description 10
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 claims description 8
- 238000007906 compression Methods 0.000 claims description 8
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- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 7
- 238000011084 recovery Methods 0.000 claims description 6
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 claims description 3
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052775 Thulium Inorganic materials 0.000 claims description 2
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims description 2
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- 230000000630 rising effect Effects 0.000 abstract 1
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- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 17
- 230000004927 fusion Effects 0.000 description 16
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- 229910052799 carbon Inorganic materials 0.000 description 12
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- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 description 11
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- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
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- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 description 6
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical class C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 6
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical class C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 6
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- 238000011088 calibration curve Methods 0.000 description 6
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- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 6
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- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
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- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 4
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 4
- WTQBISBWKRKLIJ-UHFFFAOYSA-N 5-methylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C)CC1C=C2 WTQBISBWKRKLIJ-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 4
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- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 3
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- QVLAWKAXOMEXPM-DICFDUPASA-N 1,1,1,2-tetrachloro-2,2-dideuterioethane Chemical compound [2H]C([2H])(Cl)C(Cl)(Cl)Cl QVLAWKAXOMEXPM-DICFDUPASA-N 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 2
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- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000007666 vacuum forming Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- C08F2/00—Processes of polymerisation
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
-
- 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
- C08F297/06—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 coordination type
- C08F297/08—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 coordination type polymerising mono-olefins
-
- 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
- C08F297/06—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 coordination type
- C08F297/08—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 coordination type polymerising mono-olefins
- C08F297/083—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 coordination type polymerising mono-olefins the monomers being ethylene or propylene
-
- 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
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78274606P | 2006-03-15 | 2006-03-15 | |
| PCT/US2007/064036 WO2007106881A1 (en) | 2006-03-15 | 2007-03-15 | Propylene/alpha-olefins block interpolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2008011718A true MX2008011718A (es) | 2008-11-25 |
Family
ID=38325347
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2008011718A MX2008011718A (es) | 2006-03-15 | 2007-03-15 | Interpolimeros de bloques de propileno/alfa-olefina. |
Country Status (14)
| Country | Link |
|---|---|
| EP (1) | EP2001916A1 (OSRAM) |
| JP (1) | JP2009530446A (OSRAM) |
| KR (1) | KR101386349B1 (OSRAM) |
| CN (1) | CN101405311B (OSRAM) |
| AR (1) | AR060034A1 (OSRAM) |
| AU (1) | AU2007226554A1 (OSRAM) |
| BR (2) | BRPI0709319B1 (OSRAM) |
| CA (1) | CA2644907A1 (OSRAM) |
| MX (1) | MX2008011718A (OSRAM) |
| RU (1) | RU2008140737A (OSRAM) |
| SG (1) | SG170126A1 (OSRAM) |
| TW (1) | TW200738759A (OSRAM) |
| WO (1) | WO2007106881A1 (OSRAM) |
| ZA (1) | ZA200807716B (OSRAM) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2238188B1 (en) * | 2008-01-30 | 2019-01-16 | Dow Global Technologies LLC | Butene/ -olefin block interpol ymers |
| CN101981073A (zh) * | 2008-01-30 | 2011-02-23 | 陶氏环球技术公司 | 丙烯/α-烯烃嵌段互聚物 |
| US8293859B2 (en) * | 2008-01-30 | 2012-10-23 | Dow Global Technologies, Llc | Butene/α-olefin block interpolymers |
| KR101668120B1 (ko) * | 2008-01-30 | 2016-10-20 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/α-올레핀 블록 혼성중합체 |
| CN104356324A (zh) * | 2008-01-30 | 2015-02-18 | 陶氏环球技术有限责任公司 | 丙烯/α-烯烃嵌段互聚物 |
| KR101613165B1 (ko) * | 2008-01-30 | 2016-04-18 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/α-올레핀 블록 혼성중합체 |
| CN102239213A (zh) * | 2008-10-03 | 2011-11-09 | 陶氏环球技术有限责任公司 | 具有乙烯/α-烯烃互聚物的聚合物共混物 |
| KR101795085B1 (ko) * | 2009-10-02 | 2017-11-07 | 다우 글로벌 테크놀로지스 엘엘씨 | 열가소성 가황물 응용에서의 블록 복합체 |
| MX339837B (es) * | 2010-06-18 | 2016-06-14 | Dow Global Tech Llc * | Composiciones de copolimero multibloque de olefina separada en mesofase, electricamente conductoras. |
| US9062146B2 (en) | 2011-01-20 | 2015-06-23 | Lg Chem, Ltd. | Olefin block copolymer |
| KR101262308B1 (ko) * | 2011-01-21 | 2013-05-08 | 주식회사 엘지화학 | 올레핀 블록 공중합체 및 이의 제조 방법 |
| US10023771B2 (en) * | 2014-08-21 | 2018-07-17 | Dow Global Technologies Llc | Hot melt adhesive composition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2012729C (en) * | 1989-04-07 | 1997-05-20 | Takashi Kuroda | Dulled stretched molding and process for producing the same |
| US6960635B2 (en) * | 2001-11-06 | 2005-11-01 | Dow Global Technologies Inc. | Isotactic propylene copolymers, their preparation and use |
| US7504347B2 (en) * | 2004-03-17 | 2009-03-17 | Dow Global Technologies Inc. | Fibers made from copolymers of propylene/α-olefins |
| AU2005224257B2 (en) * | 2004-03-17 | 2010-08-19 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for higher olefin multi-block copolymer formation |
| KR101506824B1 (ko) * | 2005-03-17 | 2015-03-30 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/α-올레핀 블록 혼성중합체 |
| BRPI0609849B1 (pt) * | 2005-03-17 | 2017-05-09 | Dow Global Technologies Inc | copolímero multibloco, processo de solução contínuo para preparar um copolímero multibloco, derivado funcionalizado, mistura polimérica homogênea e polímero |
-
2007
- 2007-03-15 CN CN2007800089511A patent/CN101405311B/zh active Active
- 2007-03-15 BR BRPI0709319-5A patent/BRPI0709319B1/pt not_active IP Right Cessation
- 2007-03-15 WO PCT/US2007/064036 patent/WO2007106881A1/en not_active Ceased
- 2007-03-15 TW TW096108908A patent/TW200738759A/zh unknown
- 2007-03-15 AU AU2007226554A patent/AU2007226554A1/en not_active Abandoned
- 2007-03-15 MX MX2008011718A patent/MX2008011718A/es active IP Right Grant
- 2007-03-15 KR KR1020087025020A patent/KR101386349B1/ko active Active
- 2007-03-15 AR ARP070101060A patent/AR060034A1/es unknown
- 2007-03-15 CA CA002644907A patent/CA2644907A1/en not_active Abandoned
- 2007-03-15 ZA ZA200807716A patent/ZA200807716B/xx unknown
- 2007-03-15 RU RU2008140737/04A patent/RU2008140737A/ru not_active Application Discontinuation
- 2007-03-15 SG SG201101855-3A patent/SG170126A1/en unknown
- 2007-03-15 EP EP07758577A patent/EP2001916A1/en not_active Withdrawn
- 2007-03-15 BR BR122018075054-5A patent/BR122018075054B1/pt not_active IP Right Cessation
- 2007-03-15 JP JP2009500602A patent/JP2009530446A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| RU2008140737A (ru) | 2010-04-20 |
| CA2644907A1 (en) | 2007-09-20 |
| CN101405311A (zh) | 2009-04-08 |
| EP2001916A1 (en) | 2008-12-17 |
| BR122018075054B1 (pt) | 2019-08-20 |
| BRPI0709319B1 (pt) | 2019-03-19 |
| KR20080111472A (ko) | 2008-12-23 |
| JP2009530446A (ja) | 2009-08-27 |
| TW200738759A (en) | 2007-10-16 |
| WO2007106881A1 (en) | 2007-09-20 |
| BRPI0709319A2 (pt) | 2011-07-12 |
| CN101405311B (zh) | 2012-05-09 |
| SG170126A1 (en) | 2011-04-29 |
| AR060034A1 (es) | 2008-05-21 |
| KR101386349B1 (ko) | 2014-04-16 |
| AU2007226554A1 (en) | 2007-09-20 |
| ZA200807716B (en) | 2010-01-27 |
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Legal Events
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| HC | Change of company name or juridical status |
Owner name: ABBVIE INC. |
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| FG | Grant or registration |