JP2018500430A5 - - Google Patents
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- JP2018500430A5 JP2018500430A5 JP2017533759A JP2017533759A JP2018500430A5 JP 2018500430 A5 JP2018500430 A5 JP 2018500430A5 JP 2017533759 A JP2017533759 A JP 2017533759A JP 2017533759 A JP2017533759 A JP 2017533759A JP 2018500430 A5 JP2018500430 A5 JP 2018500430A5
- Authority
- JP
- Japan
- Prior art keywords
- hydrocarbyl
- group
- zinc
- aluminum
- metal
- 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.)
- Granted
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- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 42
- -1 O 2 Inorganic materials 0.000 claims description 36
- 229910052751 metal Inorganic materials 0.000 claims description 35
- 239000002184 metal Substances 0.000 claims description 35
- 238000000034 method Methods 0.000 claims description 29
- 229920000098 polyolefin Polymers 0.000 claims description 20
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 14
- 229910052725 zinc Inorganic materials 0.000 claims description 12
- 239000011701 zinc Substances 0.000 claims description 12
- 150000001336 alkenes Chemical class 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 10
- 239000000178 monomer Substances 0.000 claims description 10
- 239000012986 chain transfer agent Substances 0.000 claims description 9
- 239000012685 metal catalyst precursor Substances 0.000 claims description 9
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- 239000007800 oxidant agent Substances 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052733 gallium Inorganic materials 0.000 claims description 6
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- 229910052726 zirconium Inorganic materials 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 230000003647 oxidation Effects 0.000 claims description 5
- 238000007254 oxidation reaction Methods 0.000 claims description 5
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 claims description 4
- VQOXUMQBYILCKR-UHFFFAOYSA-N 1-Tridecene Chemical compound CCCCCCCCCCCC=C VQOXUMQBYILCKR-UHFFFAOYSA-N 0.000 claims description 4
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 claims description 4
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 claims description 4
- ADOBXTDBFNCOBN-UHFFFAOYSA-N 1-heptadecene Chemical compound CCCCCCCCCCCCCCCC=C ADOBXTDBFNCOBN-UHFFFAOYSA-N 0.000 claims description 4
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 claims description 4
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 4
- PJLHTVIBELQURV-UHFFFAOYSA-N 1-pentadecene Chemical compound CCCCCCCCCCCCCC=C PJLHTVIBELQURV-UHFFFAOYSA-N 0.000 claims description 4
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 claims description 4
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 claims description 4
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 150000004678 hydrides Chemical class 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 4
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 claims description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims description 4
- 230000000737 periodic effect Effects 0.000 claims description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 3
- 239000012018 catalyst precursor Substances 0.000 claims description 3
- 229910052735 hafnium Inorganic materials 0.000 claims description 3
- 238000010791 quenching Methods 0.000 claims description 3
- 230000000171 quenching effect Effects 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 claims description 2
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 claims description 2
- KLAWFKRMCIXRFS-UHFFFAOYSA-N 5-ethenylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C=C)CC1C=C2 KLAWFKRMCIXRFS-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- IQEPEDROVHGOAR-UHFFFAOYSA-N C(C(C)C)[Al](CCC=C)CC(C)C Chemical compound C(C(C)C)[Al](CCC=C)CC(C)C IQEPEDROVHGOAR-UHFFFAOYSA-N 0.000 claims description 2
- HXHXUOYNZWHFLT-UHFFFAOYSA-N C(CCCC=C)[Al](CCCCC=C)CCCCC=C Chemical compound C(CCCC=C)[Al](CCCCC=C)CCCCC=C HXHXUOYNZWHFLT-UHFFFAOYSA-N 0.000 claims description 2
- HEMYFEFGZYYQSU-UHFFFAOYSA-N C=CCCCCCC[Zn]CCCCCCC=C Chemical compound C=CCCCCCC[Zn]CCCCCCC=C HEMYFEFGZYYQSU-UHFFFAOYSA-N 0.000 claims description 2
- ZXDAZVCFYFCCLZ-UHFFFAOYSA-N C=CCCCC[Zn]CCCCC=C Chemical compound C=CCCCC[Zn]CCCCC=C ZXDAZVCFYFCCLZ-UHFFFAOYSA-N 0.000 claims description 2
- PHUYKZNPNVDCIC-UHFFFAOYSA-N CC[Zn]CCCCC=C Chemical compound CC[Zn]CCCCC=C PHUYKZNPNVDCIC-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 239000007983 Tris buffer Substances 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000008064 anhydrides Chemical class 0.000 claims description 2
- 150000001541 aziridines Chemical class 0.000 claims description 2
- GMDSGSPTIDDIAZ-UHFFFAOYSA-N bis(2-methylpropyl)-oct-7-enylalumane Chemical compound CC(C)C[Al](CC(C)C)CCCCCCC=C GMDSGSPTIDDIAZ-UHFFFAOYSA-N 0.000 claims description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims description 2
- 229910010277 boron hydride Inorganic materials 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 229940069096 dodecene Drugs 0.000 claims description 2
- 150000002118 epoxides Chemical class 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 238000007306 functionalization reaction Methods 0.000 claims description 2
- DYSCYJQZDQCNEG-UHFFFAOYSA-N hex-5-enyl-bis(2-methylpropyl)alumane Chemical compound C(C(C)C)[Al](CCCCC=C)CC(C)C DYSCYJQZDQCNEG-UHFFFAOYSA-N 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 229910012375 magnesium hydride Inorganic materials 0.000 claims description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052759 nickel 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
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 2
- KYOZLPKCURERER-UHFFFAOYSA-N tris(but-3-enyl)alumane Chemical compound C=CCC[Al](CCC=C)CCC=C KYOZLPKCURERER-UHFFFAOYSA-N 0.000 claims description 2
- RRWJQXJVEHEZJR-UHFFFAOYSA-N tris(oct-7-enyl)alumane Chemical compound C=CCCCCCC[Al](CCCCCCC=C)CCCCCCC=C RRWJQXJVEHEZJR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- 229910000051 zinc hydride Inorganic materials 0.000 claims description 2
- ZULTYUIALNTCSA-UHFFFAOYSA-N zinc hydride Chemical compound [ZnH2] ZULTYUIALNTCSA-UHFFFAOYSA-N 0.000 claims description 2
- 239000004711 α-olefin Substances 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 229910007926 ZrCl Inorganic materials 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- OTTZHAVKAVGASB-UHFFFAOYSA-N hept-2-ene Chemical compound CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- ZMZGFLUUZLELNE-UHFFFAOYSA-N 2,3,5-triiodobenzoic acid Chemical compound OC(=O)C1=CC(I)=CC(I)=C1I ZMZGFLUUZLELNE-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- ZMVFRPYKRCLPGS-UHFFFAOYSA-N C(C)[Zn]CCCCCCC=C Chemical compound C(C)[Zn]CCCCCCC=C ZMVFRPYKRCLPGS-UHFFFAOYSA-N 0.000 description 1
- VHNNPTGLWYHNHE-UHFFFAOYSA-N C1=CC2=CC=CC=C2C1[Zr]C1C2=CC=CC=C2C=C1 Chemical compound C1=CC2=CC=CC=C2C1[Zr]C1C2=CC=CC=C2C=C1 VHNNPTGLWYHNHE-UHFFFAOYSA-N 0.000 description 1
- FUOMUPVKZHJNHJ-UHFFFAOYSA-N CCC=C[Zn]CC Chemical compound CCC=C[Zn]CC FUOMUPVKZHJNHJ-UHFFFAOYSA-N 0.000 description 1
- NDJMNNSJDIFFTH-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 NDJMNNSJDIFFTH-UHFFFAOYSA-L 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- ZMMRKRFMSDTOLV-UHFFFAOYSA-N cyclopenta-1,3-diene zirconium Chemical compound [Zr].C1C=CC=C1.C1C=CC=C1 ZMMRKRFMSDTOLV-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000003754 zirconium Chemical class 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14200124.7 | 2014-12-23 | ||
| EP14200124.7A EP3037437A1 (en) | 2014-12-23 | 2014-12-23 | Process for the preparation of a polyolefin having one or multiple end-functionalized branches. |
| PCT/EP2015/081207 WO2016102694A1 (en) | 2014-12-23 | 2015-12-23 | Process for the preparation of a polyolefin having one or multiple end-functionalized branches |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018500430A JP2018500430A (ja) | 2018-01-11 |
| JP2018500430A5 true JP2018500430A5 (OSRAM) | 2018-11-22 |
| JP7115852B2 JP7115852B2 (ja) | 2022-08-09 |
Family
ID=52130159
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017533759A Active JP7115852B2 (ja) | 2014-12-23 | 2015-12-23 | 一又は複数の末端官能化された分岐を有するポリオレフィンの調製方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10465018B2 (OSRAM) |
| EP (2) | EP3037437A1 (OSRAM) |
| JP (1) | JP7115852B2 (OSRAM) |
| KR (1) | KR102470347B1 (OSRAM) |
| CN (1) | CN107223138B (OSRAM) |
| SA (1) | SA517381806B1 (OSRAM) |
| WO (1) | WO2016102694A1 (OSRAM) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108137748B (zh) * | 2015-07-23 | 2021-05-04 | Sabic环球技术有限责任公司 | 用于制备具有一个或多个侧官能团的聚烯烃的方法 |
| US10829569B2 (en) * | 2015-08-31 | 2020-11-10 | Exxonmobil Chemical Patents Inc. | Polymers produced via use of vinyl transfer agents |
| US11041029B2 (en) | 2015-08-31 | 2021-06-22 | Exxonmobil Chemical Patents Inc. | Aluminum alkyls with pendant olefins for polyolefin reactions |
| US10618988B2 (en) | 2015-08-31 | 2020-04-14 | Exxonmobil Chemical Patents Inc. | Branched propylene polymers produced via use of vinyl transfer agents and processes for production thereof |
| US10676547B2 (en) | 2015-08-31 | 2020-06-09 | Exxonmobil Chemical Patents Inc. | Aluminum alkyls with pendant olefins on clays |
| CN108291032B (zh) * | 2015-12-09 | 2021-01-26 | Sabic环球技术有限责任公司 | 用于制备包含第一长链支化聚烯烃嵌段和一个或多个聚合物侧链的聚烯烃接枝共聚物的方法 |
| US10562987B2 (en) | 2016-06-30 | 2020-02-18 | Exxonmobil Chemical Patents Inc. | Polymers produced via use of quinolinyldiamido transition metal complexes and vinyl transfer agents |
| US10927196B2 (en) | 2016-06-30 | 2021-02-23 | Exxonmobil Chemical Patents Inc. | Long chain branched polypropylene via polymerization with aluminum vinyl transfer agent |
| US10626200B2 (en) | 2017-02-28 | 2020-04-21 | Exxonmobil Chemical Patents Inc. | Branched EPDM polymers produced via use of vinyl transfer agents and processes for production thereof |
| US10676551B2 (en) * | 2017-03-01 | 2020-06-09 | Exxonmobil Chemical Patents Inc. | Branched ethylene copolymers produced via use of vinyl transfer agents and processes for production thereof |
| EP3728348A1 (en) * | 2017-12-22 | 2020-10-28 | SABIC Global Technologies B.V. | Process for preparation of semi-crystalline polyolefinic ionomers |
| JP7381464B2 (ja) * | 2017-12-29 | 2023-11-15 | ダウ グローバル テクノロジーズ エルエルシー | 末端保護された双頭型有機アルミニウム組成物 |
| CN109467660B (zh) * | 2018-10-06 | 2021-03-02 | 天津大学 | 利用链穿梭方法合成聚(乙烯-r-降冰片烯/乙烯)多嵌段共聚物 |
| WO2020139993A1 (en) * | 2018-12-28 | 2020-07-02 | Dow Global Technologies Llc | Curable compositions comprising unsaturated polyolefins |
| JP2022516120A (ja) * | 2018-12-28 | 2022-02-24 | ダウ グローバル テクノロジーズ エルエルシー | 有機金属連鎖移動剤 |
| CN111116811B (zh) * | 2020-01-03 | 2022-07-05 | 天津大学 | 一种1-丁烯/降冰片烯共聚物及其制备方法 |
| WO2022029213A1 (en) * | 2020-08-06 | 2022-02-10 | Total Research & Technology Feluy | Process for preparing ethylene polymers having long chain branches |
| US12195563B2 (en) * | 2020-12-29 | 2025-01-14 | Exxonmobil Chemical Patents Inc. | Polyolefin-based ionomers and production thereof |
| BR112023020957A2 (pt) * | 2021-04-30 | 2023-12-12 | Dow Global Technologies Llc | Método para preparar uma poliolefina, poliolefina, e, tensoativo |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5077357A (en) | 1990-10-22 | 1991-12-31 | Shell Oil Company | Olefin polymerization catalyst |
| US5106806A (en) | 1990-10-18 | 1992-04-21 | Shell Oil Company | Olefin polymerization catalyst |
| CA1141093A (en) | 1979-05-17 | 1983-02-08 | Brian L. Goodall | Olefin polymerization catalyst compositions and a process for the polymerization of olefins employing such compositions |
| JPS61151202A (ja) * | 1984-12-26 | 1986-07-09 | Toa Nenryo Kogyo Kk | プロピレン重合体の製造法 |
| IT1227259B (it) | 1988-09-30 | 1991-03-28 | Himont Inc | Catalizzatori per la polimerizzazione di olefine. |
| US5556820A (en) | 1989-12-28 | 1996-09-17 | Idemitsu Petrochemical Co., Ltd. | Catalyst component for olefin polymerization and process for producing polyolefins |
| US5374696A (en) | 1992-03-26 | 1994-12-20 | The Dow Chemical Company | Addition polymerization process using stabilized reduced metal catalysts |
| NL9201970A (nl) | 1992-11-11 | 1994-06-01 | Dsm Nv | Indenylverbindingen en katalysatorcomponenten voor de polymerisatie van olefinen. |
| US5468819A (en) * | 1993-11-16 | 1995-11-21 | The B.F. Goodrich Company | Process for making polymers containing a norbornene repeating unit by addition polymerization using an organo (nickel or palladium) complex |
| US5472785A (en) * | 1994-04-12 | 1995-12-05 | Minnesota Mining And Manufacturing Company | Reactive wax-containing moisture curable hot melt composition |
| JP3719727B2 (ja) * | 1994-10-13 | 2005-11-24 | 三井化学株式会社 | 末端に官能基を有するポリオレフィンの製造方法 |
| BR9509457A (pt) | 1994-10-31 | 1998-01-06 | Dsm Nv | Composição catalítica e processo para a polimerização de uma olefina |
| WO1996032426A1 (en) | 1995-04-10 | 1996-10-17 | Dsm N.V. | Method for the preparation of a catalyst suitable for the polymerisation of an olefine |
| US5756416A (en) * | 1995-11-28 | 1998-05-26 | Union Carbide Chemicals & Plastics Technology Corporation | Catalyst composition having improved comonomer reactivity |
| WO1997042232A1 (en) | 1996-05-03 | 1997-11-13 | Dsm N.V. | Process for the polymerisation of alpha-olefins |
| AU2653097A (en) | 1996-05-03 | 1997-11-26 | Dsm N.V. | Process for the production of functional polyolefins |
| US6248837B1 (en) * | 1996-07-15 | 2001-06-19 | The Penn State Research Foundation | Process for preparing polyolefin diblock copolymers involving borane chain transfer reaction in transition metal-mediated olefin polymerization |
| US6208151B1 (en) * | 1997-12-23 | 2001-03-27 | Texas Instruments Incorporated | Method and apparatus for measurement of microscopic electrical characteristics |
| ES2224600T3 (es) * | 1998-02-11 | 2005-03-01 | Dow Global Technologies Inc. | Procedimiento de polimerizacion de olefinas mejorado. |
| KR100280373B1 (ko) * | 1998-09-18 | 2001-02-01 | 김충섭 | 메탈로센 촉매에 의한 관능성 말단기를 갖는 폴리에틸렌의 제조방법 |
| US6583237B1 (en) | 1999-01-22 | 2003-06-24 | Mitsui Chemicals, Inc. | Process for producing olefin polymer and olefin polymers |
| US6342622B1 (en) | 1999-06-11 | 2002-01-29 | Dsm B.V. | Indenyl compounds for the polymerization of olefins |
| EP1086961A1 (en) | 1999-09-27 | 2001-03-28 | Dsm N.V. | Process for the preparation of a catalyst component for the polymerisation of an olefin |
| JP2001278928A (ja) * | 2000-01-25 | 2001-10-10 | Mitsui Chemicals Inc | フィルムおよびシート |
| BR0204687B1 (pt) | 2001-03-30 | 2012-12-11 | componente de catalisador sólido para a polimerização de olefinas, catalisador para a polimerização de olefinas, e, copolìmero em bloco de propileno. | |
| US7087686B2 (en) | 2001-08-06 | 2006-08-08 | Bp Chemicals Limited | Chain growth reaction process |
| JP3891905B2 (ja) * | 2002-08-28 | 2007-03-14 | 日本ポリプロ株式会社 | 末端ビニル基含有プロピレン−アルケニルアルミニウム共重合体の製造方法および共重合体 |
| WO2004081064A1 (ja) | 2003-03-10 | 2004-09-23 | Asahi Kasei Chemicals Corporation | 超高分子量エチレン系重合体 |
| JP4879882B2 (ja) | 2004-03-17 | 2012-02-22 | ダウ グローバル テクノロジーズ エルエルシー | より高次のオレフィンマルチブロックコポリマーを形成するためのシャトリング剤を含む触媒組成物 |
| JP4439323B2 (ja) * | 2004-04-26 | 2010-03-24 | 独立行政法人産業技術総合研究所 | 極性基含有共重合体及びその製造方法 |
| ES2317273T3 (es) | 2004-07-30 | 2009-04-16 | Saudi Basic Industries Corporation | Composiciones de copolimero de propileno con elevada transparencia. |
| TW200722441A (en) * | 2005-09-15 | 2007-06-16 | Dow Global Technologies Inc | Catalytic olefin block copolymers via polymerizable shuttling agent |
| JP2007262338A (ja) * | 2006-03-29 | 2007-10-11 | Japan Polypropylene Corp | 極性基を有すプロピレン系共重合体又はその組成物を用いた塗装用成形品 |
| EA013392B1 (ru) | 2006-05-24 | 2010-04-30 | Сауди Бейсик Индастриз Корпорейшн | Способ получения каталитического компонента для полимеризации пропилена |
| BR112012001942B1 (pt) | 2009-07-29 | 2019-10-22 | Dow Global Technologies Llc | agente de permuta de cadeia multifuncional, processo para preparar um agente de permuta de cadeia multifuncional, processo para preparar uma composição multifuncional, composição multifuncional, processo para preparar um agente de permuta de cadeia multifuncional contendo poli-radical poliolefina, poliolefina telequélica, processo para preparar uma poliolefina com funcionalidade terminal e separador de bateria |
| KR102001440B1 (ko) | 2011-12-12 | 2019-07-18 | 사우디 베이식 인더스트리즈 코포레이션 | 촉매 시스템의 존재 하에 2형식 폴리에틸렌을 생산하는 방법 |
| EP2671639B1 (en) * | 2012-06-04 | 2017-01-11 | Sasol Performance Chemicals GmbH | Guanidinate complexes and their use as chain transfer polymerization catalysts |
| EP2880097B1 (en) | 2012-08-03 | 2023-10-18 | ExxonMobil Chemical Patents Inc. | Process to prepare a vinyl terminated polyethylene with long chain branching |
| EP2880006B1 (en) | 2012-08-03 | 2017-12-20 | ExxonMobil Chemical Patents Inc. | Non-symmetric catalysts comprising salan ligands |
| WO2014022008A1 (en) | 2012-08-03 | 2014-02-06 | Exxonmobil Chemical Patents Inc. | Catalysts comprising salan ligands |
-
2014
- 2014-12-23 EP EP14200124.7A patent/EP3037437A1/en not_active Withdrawn
-
2015
- 2015-12-23 WO PCT/EP2015/081207 patent/WO2016102694A1/en not_active Ceased
- 2015-12-23 EP EP15823164.7A patent/EP3237461A1/en active Pending
- 2015-12-23 JP JP2017533759A patent/JP7115852B2/ja active Active
- 2015-12-23 CN CN201580075823.3A patent/CN107223138B/zh active Active
- 2015-12-23 KR KR1020177020265A patent/KR102470347B1/ko active Active
- 2015-12-23 US US15/537,933 patent/US10465018B2/en active Active
-
2017
- 2017-06-22 SA SA517381806A patent/SA517381806B1/ar unknown
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