BG60380B1 - МЕТОД ЗА ОТСТРАНЯВАНЕ НА ПРИМЕСИ ОТ TiCl4 В ТЕЧНА ФАЗА - Google Patents
МЕТОД ЗА ОТСТРАНЯВАНЕ НА ПРИМЕСИ ОТ TiCl4 В ТЕЧНА ФАЗА Download PDFInfo
- Publication number
- BG60380B1 BG60380B1 BG78546A BG7854687A BG60380B1 BG 60380 B1 BG60380 B1 BG 60380B1 BG 78546 A BG78546 A BG 78546A BG 7854687 A BG7854687 A BG 7854687A BG 60380 B1 BG60380 B1 BG 60380B1
- Authority
- BG
- Bulgaria
- Prior art keywords
- liquid phase
- ticl
- formula
- group
- solid
- Prior art date
Links
- 239000007791 liquid phase Substances 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 title claims abstract description 25
- 239000012535 impurity Substances 0.000 title claims abstract description 11
- 229910003074 TiCl4 Inorganic materials 0.000 title abstract 3
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 title abstract 3
- -1 organic acid halide Chemical class 0.000 claims abstract description 20
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 125000003118 aryl group Chemical group 0.000 claims abstract description 12
- 239000007787 solid Substances 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 229930195733 hydrocarbon Natural products 0.000 claims description 10
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 7
- 230000003197 catalytic effect Effects 0.000 claims description 6
- 150000004820 halides Chemical class 0.000 claims description 6
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 239000012265 solid product Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 239000011949 solid catalyst Substances 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 4
- 239000002244 precipitate Substances 0.000 abstract 1
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 6
- 238000001914 filtration Methods 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- AVGQTJUPLKNPQP-UHFFFAOYSA-N 1,1,1-trichloropropane Chemical compound CCC(Cl)(Cl)Cl AVGQTJUPLKNPQP-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- IBSQPLPBRSHTTG-UHFFFAOYSA-N 1-chloro-2-methylbenzene Chemical compound CC1=CC=CC=C1Cl IBSQPLPBRSHTTG-UHFFFAOYSA-N 0.000 description 1
- BSPCSKHALVHRSR-UHFFFAOYSA-N 2-chlorobutane Chemical compound CCC(C)Cl BSPCSKHALVHRSR-UHFFFAOYSA-N 0.000 description 1
- HRAQMGWTPNOILP-UHFFFAOYSA-N 4-Ethoxy ethylbenzoate Chemical compound CCOC(=O)C1=CC=C(OCC)C=C1 HRAQMGWTPNOILP-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000002879 Lewis base Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- UEHLUKOPEIIXIA-UHFFFAOYSA-N [Mg].COCl Chemical compound [Mg].COCl UEHLUKOPEIIXIA-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229950005499 carbon tetrachloride Drugs 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- REBFJHPJLSHCAF-UHFFFAOYSA-N ethyl hypochlorite;magnesium Chemical compound [Mg].CCOCl REBFJHPJLSHCAF-UHFFFAOYSA-N 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 description 1
- 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 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
- 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
-
- 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Ceramic Products (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Saccharide Compounds (AREA)
- Extraction Or Liquid Replacement (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB858513000A GB8513000D0 (en) | 1985-05-22 | 1985-05-22 | Removing contaminants from liquid tici4 phase |
| PCT/EP1986/000301 WO1986007066A2 (en) | 1985-05-22 | 1986-05-16 | A process for removing contaminants from a liquid ticl4 phase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BG78546A BG78546A (bg) | 1993-12-24 |
| BG60380B1 true BG60380B1 (bg) | 1995-01-03 |
Family
ID=10579543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG78546A BG60380B1 (bg) | 1985-05-22 | 1987-02-18 | МЕТОД ЗА ОТСТРАНЯВАНЕ НА ПРИМЕСИ ОТ TiCl4 В ТЕЧНА ФАЗА |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4683215A (ko) |
| EP (1) | EP0202715B1 (ko) |
| JP (1) | JPH0764562B2 (ko) |
| KR (1) | KR940000013B1 (ko) |
| AT (1) | ATE53594T1 (ko) |
| AU (1) | AU589981B2 (ko) |
| BG (1) | BG60380B1 (ko) |
| BR (1) | BR8606682A (ko) |
| CA (1) | CA1254899A (ko) |
| DE (1) | DE3671899D1 (ko) |
| DK (1) | DK27587D0 (ko) |
| DZ (1) | DZ921A1 (ko) |
| EG (1) | EG18134A (ko) |
| ES (1) | ES8707160A1 (ko) |
| GB (1) | GB8513000D0 (ko) |
| HU (1) | HU199515B (ko) |
| IN (2) | IN171621B (ko) |
| NO (1) | NO170546C (ko) |
| NZ (1) | NZ216237A (ko) |
| TR (1) | TR22390A (ko) |
| WO (1) | WO1986007066A2 (ko) |
| ZA (1) | ZA863760B (ko) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4914257A (en) * | 1988-05-23 | 1990-04-03 | Amoco Corporation | Method and apparatus for recovering high purity toluene, hexane, titanium tetrachloride and tetrahydrofuran from mixtures |
| CA2478105A1 (en) | 2002-03-04 | 2003-09-12 | Akzo Nobel Nv | Treatment of a titanium tetrachloride-containing waste stream |
| JP4540055B2 (ja) * | 2005-03-30 | 2010-09-08 | 東邦チタニウム株式会社 | オレフィン類重合用固体触媒成分の製造方法 |
| WO2009116057A2 (en) * | 2008-03-18 | 2009-09-24 | Reliance Industries Limited | A process for the synthesis of alpha-olefin polymerization procatalysts |
| CN104129812B (zh) * | 2013-05-03 | 2015-09-16 | 中国石油化工股份有限公司 | 一种含钛废液的处理方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1809223A (en) * | 1928-05-15 | 1931-06-09 | Armen H Tashjian | Combined conduit and molding |
| GB1148184A (en) * | 1966-07-08 | 1969-04-10 | Henning Jorgensen | Improvements in or relating to ducts for enclosing electrical wiring in buildings |
| IT1042711B (it) * | 1975-09-19 | 1980-01-30 | Montedison Spa | Compnenti di catalizzatori per la polimerizzazione di olefine |
| DE2831830A1 (de) * | 1978-07-20 | 1980-01-31 | Basf Ag | Verfahren zum herstellen einer komponente fuer polymerisationskatalysatoren |
| EP0019312B1 (en) * | 1979-04-30 | 1983-08-17 | Shell Internationale Researchmaatschappij B.V. | Olefin polymerization catalyst compositions and a process for the polymerization of olefins employing such compositions |
| 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 |
| EP0085231B1 (en) * | 1981-12-17 | 1986-11-12 | Imperial Chemical Industries Plc | Catalyst composition, production and use |
| US4535068A (en) * | 1983-09-20 | 1985-08-13 | Shell Oil Company | Olefin polymerization catalyst compositions and polymerization process |
| IN163585B (ko) * | 1983-09-20 | 1988-10-15 | Shell Int Research |
-
1985
- 1985-05-22 GB GB858513000A patent/GB8513000D0/en active Pending
-
1986
- 1986-05-02 CA CA000508204A patent/CA1254899A/en not_active Expired
- 1986-05-08 US US06/860,941 patent/US4683215A/en not_active Expired - Lifetime
- 1986-05-16 HU HU863268A patent/HU199515B/hu not_active IP Right Cessation
- 1986-05-16 AU AU59600/86A patent/AU589981B2/en not_active Ceased
- 1986-05-16 DE DE8686200852T patent/DE3671899D1/de not_active Expired - Lifetime
- 1986-05-16 AT AT86200852T patent/ATE53594T1/de active
- 1986-05-16 JP JP61503170A patent/JPH0764562B2/ja not_active Expired - Lifetime
- 1986-05-16 KR KR1019860700933A patent/KR940000013B1/ko not_active IP Right Cessation
- 1986-05-16 EP EP86200852A patent/EP0202715B1/en not_active Expired - Lifetime
- 1986-05-16 BR BR8606682A patent/BR8606682A/pt not_active IP Right Cessation
- 1986-05-16 WO PCT/EP1986/000301 patent/WO1986007066A2/en unknown
- 1986-05-20 TR TR26595/86A patent/TR22390A/xx unknown
- 1986-05-20 NZ NZ216237A patent/NZ216237A/xx unknown
- 1986-05-20 DZ DZ860090A patent/DZ921A1/fr active
- 1986-05-20 IN IN448/DEL/86A patent/IN171621B/en unknown
- 1986-05-20 ES ES555134A patent/ES8707160A1/es not_active Expired
- 1986-05-20 ZA ZA863760A patent/ZA863760B/xx unknown
- 1986-05-21 EG EG299/86A patent/EG18134A/xx active
-
1987
- 1987-01-19 DK DK027587A patent/DK27587D0/da not_active Application Discontinuation
- 1987-01-21 NO NO870260A patent/NO170546C/no not_active IP Right Cessation
- 1987-02-18 BG BG78546A patent/BG60380B1/bg unknown
-
1988
- 1988-07-15 IN IN607/DEL/88A patent/IN171800B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA1254899A (en) | 1989-05-30 |
| DK27587A (da) | 1987-01-19 |
| BR8606682A (pt) | 1987-08-11 |
| WO1986007066A3 (en) | 1986-12-31 |
| JPH0764562B2 (ja) | 1995-07-12 |
| DK27587D0 (da) | 1987-01-19 |
| EG18134A (en) | 1992-08-30 |
| ZA863760B (en) | 1987-07-29 |
| NO170546B (no) | 1992-07-20 |
| ATE53594T1 (de) | 1990-06-15 |
| IN171621B (ko) | 1992-11-28 |
| BG78546A (bg) | 1993-12-24 |
| DE3671899D1 (de) | 1990-07-19 |
| DZ921A1 (fr) | 2004-09-13 |
| EP0202715A1 (en) | 1986-11-26 |
| KR870700226A (ko) | 1987-05-30 |
| HU199515B (en) | 1990-02-28 |
| AU5960086A (en) | 1986-12-24 |
| EP0202715B1 (en) | 1990-06-13 |
| GB8513000D0 (en) | 1985-06-26 |
| WO1986007066A2 (en) | 1986-12-04 |
| NZ216237A (en) | 1989-06-28 |
| NO870260L (no) | 1987-01-21 |
| AU589981B2 (en) | 1989-10-26 |
| US4683215A (en) | 1987-07-28 |
| NO170546C (no) | 1992-10-28 |
| ES8707160A1 (es) | 1987-07-16 |
| ES555134A0 (es) | 1987-07-16 |
| TR22390A (tr) | 1987-03-19 |
| IN171800B (ko) | 1993-01-09 |
| JPS62502888A (ja) | 1987-11-19 |
| HUT43331A (en) | 1987-10-28 |
| KR940000013B1 (ko) | 1994-01-05 |
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