NO771259L - Fremgangsm}te for fremstilling av poly-alfa-olefiner - Google Patents

Fremgangsm}te for fremstilling av poly-alfa-olefiner

Info

Publication number: NO771259L
Authority: NO; Norway
Prior art keywords: compound; formula; titanium; ether; electron donor
Prior art date: 1976-04-13

Application number

NO771259A

Other languages

English (en)

Norwegian (no)

Inventor

Gerhard Staiger

Klaus Bronstert

Original Assignee

Basf Ag

Priority date (The priority date 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 date listed.)

1976-04-13

Filing date

1977-04-12

Publication date

1977-10-14

1977-04-12 Application filed by Basf Ag filed Critical Basf Ag

1977-10-14 Publication of NO771259L publication Critical patent/NO771259L/no

Links

238000000034 method Methods 0.000 title claims description 14
150000001875 compounds Chemical class 0.000 claims description 28
239000003054 catalyst Substances 0.000 claims description 23
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 18
238000000227 grinding Methods 0.000 claims description 16
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 11
229910052782 aluminium Inorganic materials 0.000 claims description 11
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 11
238000006116 polymerization reaction Methods 0.000 claims description 11
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 10
239000002245 particle Substances 0.000 claims description 10
229910052719 titanium Inorganic materials 0.000 claims description 10
239000010936 titanium Substances 0.000 claims description 10
239000004711 α-olefin Substances 0.000 claims description 9
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 6
229910000831 Steel Inorganic materials 0.000 claims description 5
229910010062 TiCl3 Inorganic materials 0.000 claims description 5
230000001133 acceleration Effects 0.000 claims description 5
239000000203 mixture Substances 0.000 claims description 5
239000010959 steel Substances 0.000 claims description 5
YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 claims description 5
239000000654 additive Substances 0.000 claims description 4
125000004430 oxygen atom Chemical group O* 0.000 claims description 4
238000010422 painting Methods 0.000 claims description 4
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
230000001747 exhibiting effect Effects 0.000 claims description 2
239000003973 paint Substances 0.000 claims description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
229910052757 nitrogen Inorganic materials 0.000 claims 1
229910052698 phosphorus Inorganic materials 0.000 claims 1
239000011574 phosphorus Substances 0.000 claims 1
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 18
150000002148 esters Chemical class 0.000 description 11
-1 polypropylene Polymers 0.000 description 7
239000000463 material Substances 0.000 description 6
AQZGPSLYZOOYQP-UHFFFAOYSA-N Diisoamyl ether Chemical compound CC(C)CCOCCC(C)C AQZGPSLYZOOYQP-UHFFFAOYSA-N 0.000 description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
238000009835 boiling Methods 0.000 description 4
HVJKZICIMIWFCP-UHFFFAOYSA-N isovalerianic acid phenylmethyl ester Natural products CC(C)CC(=O)OCC1=CC=CC=C1 HVJKZICIMIWFCP-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229920001155 polypropylene Polymers 0.000 description 3
MLLAPOCBLWUFAP-UHFFFAOYSA-N 3-Methylbutyl benzoate Chemical compound CC(C)CCOC(=O)C1=CC=CC=C1 MLLAPOCBLWUFAP-UHFFFAOYSA-N 0.000 description 2
ZSBTVXBAENDZBH-UHFFFAOYSA-N 3-methylbutoxybenzene Chemical compound CC(C)CCOC1=CC=CC=C1 ZSBTVXBAENDZBH-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
XINCECQTMHSORG-UHFFFAOYSA-N Isoamyl isovalerate Chemical compound CC(C)CCOC(=O)CC(C)C XINCECQTMHSORG-UHFFFAOYSA-N 0.000 description 2
SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
239000011261 inert gas Substances 0.000 description 2
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
229920013639 polyalphaolefin Polymers 0.000 description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
MNZAKDODWSQONA-UHFFFAOYSA-N 1-dibutylphosphorylbutane Chemical compound CCCCP(=O)(CCCC)CCCC MNZAKDODWSQONA-UHFFFAOYSA-N 0.000 description 1
BPIUIOXAFBGMNB-UHFFFAOYSA-N 1-hexoxyhexane Chemical compound CCCCCCOCCCCCC BPIUIOXAFBGMNB-UHFFFAOYSA-N 0.000 description 1
AOPDRZXCEAKHHW-UHFFFAOYSA-N 1-pentoxypentane Chemical compound CCCCCOCCCCC AOPDRZXCEAKHHW-UHFFFAOYSA-N 0.000 description 1
ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 description 1
SAWMBRUFQYQNLJ-UHFFFAOYSA-N 3-ethyl-3-(3-ethyloctan-3-yloxy)octane Chemical compound CCCCCC(CC)(CC)OC(CC)(CC)CCCCC SAWMBRUFQYQNLJ-UHFFFAOYSA-N 0.000 description 1
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-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
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
YFNONBGXNFCTMM-UHFFFAOYSA-N butoxybenzene Chemical compound CCCCOC1=CC=CC=C1 YFNONBGXNFCTMM-UHFFFAOYSA-N 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
239000011521 glass Substances 0.000 description 1
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
238000003801 milling Methods 0.000 description 1
MXHTZQSKTCCMFG-UHFFFAOYSA-N n,n-dibenzyl-1-phenylmethanamine Chemical compound C=1C=CC=CC=1CN(CC=1C=CC=CC=1)CC1=CC=CC=C1 MXHTZQSKTCCMFG-UHFFFAOYSA-N 0.000 description 1
FZPXKEPZZOEPGX-UHFFFAOYSA-N n,n-dibutylaniline Chemical compound CCCCN(CCCC)C1=CC=CC=C1 FZPXKEPZZOEPGX-UHFFFAOYSA-N 0.000 description 1
HTDCNKTXDLRMHZ-UHFFFAOYSA-N n,n-dibutylcyclohexanamine Chemical compound CCCCN(CCCC)C1CCCCC1 HTDCNKTXDLRMHZ-UHFFFAOYSA-N 0.000 description 1
MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 1
150000003003 phosphines Chemical class 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
IGNTWNVBGLNYDV-UHFFFAOYSA-N triisopropylphosphine Chemical compound CC(C)P(C(C)C)C(C)C IGNTWNVBGLNYDV-UHFFFAOYSA-N 0.000 description 1
FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
HKLUGNQYKGNLDN-UHFFFAOYSA-N tris(3-methylbutyl) borate Chemical compound CC(C)CCOB(OCCC(C)C)OCCC(C)C HKLUGNQYKGNLDN-UHFFFAOYSA-N 0.000 description 1
238000001291 vacuum drying Methods 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/906—Comminution of transition metal containing catalyst

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

NO771259A 1976-04-13 1977-04-12 Fremgangsm}te for fremstilling av poly-alfa-olefiner NO771259L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19762616260 DE2616260A1 (de)	1976-04-13	1976-04-13	Verfahren zur herstellung von poly-alpha-olefinen

Publications (1)

Publication Number	Publication Date
NO771259L true NO771259L (no)	1977-10-14

Family

ID=5975299

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO771259A NO771259L (no)	1976-04-13	1977-04-12	Fremgangsm}te for fremstilling av poly-alfa-olefiner

Country Status (16)

Country	Link
US (1)	US4296222A (de)
JP (1)	JPS52126491A (de)
AT (1)	AT349754B (de)
AU (1)	AU513824B2 (de)
BE (1)	BE853532A (de)
CA (1)	CA1079447A (de)
DE (1)	DE2616260A1 (de)
ES (1)	ES457755A1 (de)
FR (1)	FR2348229A1 (de)
GB (1)	GB1543868A (de)
IT (1)	IT1075366B (de)
NL (1)	NL7703897A (de)
NO (1)	NO771259L (de)
PT (1)	PT66410B (de)
SE (1)	SE7704183L (de)
ZA (1)	ZA772194B (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2860737D1 (en) *	1977-08-31	1981-09-03	Ici Plc	Titanium trichloride compositions, preparation thereof, catalyst system containing them, and polymerisation of olefins using this system
DE2861357D1 (en)	1977-08-31	1982-01-28	Ici Plc	Titanium trichloride compositions, preparation thereof, catalyst system containing them and polymerisation of olefins using this system
US4382018A (en) *	1979-06-27	1983-05-03	Dart Industries, Inc.	Method for making titanium trichloride catalysts
DK324084A (da) *	1983-07-21	1985-01-22	Stauffer Chemical Co	Olefinpolymerisationskatalysator og fremgangsmaade
US4563437A (en) *	1984-08-30	1986-01-07	Toho Titanium Co., Ltd.	Process for preparation of catalytic components for polymerization of α-olefins
WO1989000584A1 (en) *	1987-07-10	1989-01-26	Quantum Chemical Corporation	Propylene polymerization catalyst and method

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1128724A (en) *	1966-05-30	1968-10-02	Mitsubishi Petrochemical Co	Process for producing crystalline homopolymers or copolymers of olefin
BE791441A (fr) *	1971-11-24	1973-05-16	Solvay	Procede pour la polymerisation des alpha-olefines
DE2226167C3 (de) *	1972-05-30	1979-04-26	Basf Ag, 6700 Ludwigshafen	Verfahren zur Polymerisation von a-OIefinen

1976
- 1976-04-13 DE DE19762616260 patent/DE2616260A1/de not_active Withdrawn
1977
- 1977-03-23 CA CA274,601A patent/CA1079447A/en not_active Expired
- 1977-03-24 US US05/780,764 patent/US4296222A/en not_active Expired - Lifetime
- 1977-03-24 AU AU23577/77A patent/AU513824B2/en not_active Expired
- 1977-03-29 IT IT21835/77A patent/IT1075366B/it active
- 1977-04-06 PT PT66410A patent/PT66410B/pt unknown
- 1977-04-07 NL NL7703897A patent/NL7703897A/xx not_active Application Discontinuation
- 1977-04-12 NO NO771259A patent/NO771259L/no unknown
- 1977-04-12 JP JP4100277A patent/JPS52126491A/ja active Pending
- 1977-04-12 AT AT253777A patent/AT349754B/de not_active IP Right Cessation
- 1977-04-12 SE SE7704183A patent/SE7704183L/xx unknown
- 1977-04-12 GB GB14986/77A patent/GB1543868A/en not_active Expired
- 1977-04-12 ZA ZA00772194A patent/ZA772194B/xx unknown
- 1977-04-13 ES ES457755A patent/ES457755A1/es not_active Expired
- 1977-04-13 BE BE176661A patent/BE853532A/xx not_active IP Right Cessation
- 1977-04-13 FR FR7711088A patent/FR2348229A1/fr active Granted

Also Published As

Publication number	Publication date
SE7704183L (sv)	1977-10-14
GB1543868A (en)	1979-04-11
ATA253777A (de)	1978-09-15
IT1075366B (it)	1985-04-22
PT66410B (en)	1978-09-15
AT349754B (de)	1979-04-25
PT66410A (en)	1977-05-01
AU2357777A (en)	1978-09-28
AU513824B2 (en)	1981-01-08
BE853532A (fr)	1977-10-13
NL7703897A (nl)	1977-10-17
ZA772194B (en)	1978-04-26
US4296222A (en)	1981-10-20
FR2348229A1 (fr)	1977-11-10
JPS52126491A (en)	1977-10-24
ES457755A1 (es)	1978-02-16
DE2616260A1 (de)	1977-11-03
CA1079447A (en)	1980-06-10
FR2348229B1 (de)	1981-02-20

Publication	Publication Date	Title
CA1299807C (en)	1992-04-28	Process for producing olefin polymers and catalyst used therein
CA1206466A (en)	1986-06-24	Catalyst composition for polymerizing olefins
EP0170410B1 (de)	1989-04-05	Verfahren zur Polymerisierung oder Mischpolymerisierung von alpha-Olefinen im Wirbelbett, in Anwesenheit eines Ziegler-Natta-Katalysatorsystems
CA1151142A (en)	1983-08-02	PROCESS FOR PRODUCING .alpha.-OLEFIN POLYMERS
EP0125910B1 (de)	1986-10-08	Verfahren zur Herstellung von 4-Methyl-1-penten-Polymeren oder -Copolymeren
US4634744A (en)	1987-01-06	Method of catalyst deactivation
KR19980702201A (ko)	1998-07-15	올레핀류 중합용 고체 촉매 성분 및 촉매
KR950010650B1 (ko)	1995-09-21	프로필렌-α-올레핀 블럭 공중합체의 제조방법
KR19980018948A (ko)	1998-06-05	α-올레핀 중합용 고체 촉매 성분, α-올페핀 중합용 촉매, 및 α-올레핀 중합체의 제조 방법 (SOLID CATALYST COMPONENT FOR α-OLEFIN POLYMERIZATION, CATALYST FOR α-OLEFIN POLYMERIZATION, AND PROCESS FOR PRODUCING α-OLEFIN POLYMER)
HK48893A (en)	1993-05-27	Catalytic solid to be used in stereospecific polymerization of alpha-olefins, process for its preparation and process for polymerizing alpha-olefins in its presence
HU207870B (en)	1993-06-28	Process for producing poly-/alpha-olefine/
EP0026027B1 (de)	1983-06-08	Verfahren zur Polymerisation von alpha-Olefinen
EP0037291B1 (de)	1985-08-07	Verfahren zur Herstellung eines Propylen enthaltenden Blockcopolymers
NO771259L (no)	1977-10-14	Fremgangsm}te for fremstilling av poly-alfa-olefiner
US3752797A (en)	1973-08-14	Mixed catalyst for the polymerization of alpha olefins
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