NO119277B - - Google Patents

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Info

Publication number: NO119277B
Authority: NO; Norway
Prior art keywords: polyethylene; alcohols; stated; polymerization; polyolefins
Prior art date: 1965-06-16

Application number

NO162977A

Other languages

English (en)

Norwegian (no)

Inventor

G Regnier

R Canevari

M Laubie

Original Assignee

Science Union & Cie

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.)

1965-06-16

Filing date

1966-05-11

Publication date

1970-04-27

1966-05-11 Application filed by Science Union & Cie filed Critical Science Union & Cie

1970-04-27 Publication of NO119277B publication Critical patent/NO119277B/no

Links

-1 polyethylene Polymers 0.000 claims description 25
229920000573 polyethylene Polymers 0.000 claims description 21
239000004698 Polyethylene Substances 0.000 claims description 20
238000006116 polymerization reaction Methods 0.000 claims description 17
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 16
238000000034 method Methods 0.000 claims description 14
229920000098 polyolefin Polymers 0.000 claims description 14
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 12
239000003054 catalyst Substances 0.000 claims description 10
150000001298 alcohols Chemical class 0.000 claims description 9
238000005406 washing Methods 0.000 claims description 9
239000000203 mixture Substances 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 8
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 7
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 4
239000004743 Polypropylene Substances 0.000 claims description 3
229920001155 polypropylene Polymers 0.000 claims description 3
238000000746 purification Methods 0.000 claims description 3
239000000375 suspending agent Substances 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
239000012459 cleaning agent Substances 0.000 claims 3
150000002736 metal compounds Chemical class 0.000 claims 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
229910052799 carbon Inorganic materials 0.000 claims 1
239000007795 chemical reaction product Substances 0.000 claims 1
239000000725 suspension Substances 0.000 claims 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
239000005977 Ethylene Substances 0.000 description 10
229920000642 polymer Polymers 0.000 description 10
239000000047 product Substances 0.000 description 10
229910052782 aluminium Inorganic materials 0.000 description 9
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 8
238000001035 drying Methods 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
150000001336 alkenes Chemical class 0.000 description 4
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 3
239000007787 solid Substances 0.000 description 3
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000004411 aluminium Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000002283 diesel fuel Substances 0.000 description 2
YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000012535 impurity Substances 0.000 description 2
239000002685 polymerization catalyst Substances 0.000 description 2
YOBOXHGSEJBUPB-MTOQALJVSA-N (z)-4-hydroxypent-3-en-2-one;zirconium Chemical compound [Zr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O YOBOXHGSEJBUPB-MTOQALJVSA-N 0.000 description 1
ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
229910052776 Thorium Inorganic materials 0.000 description 1
229910010165 TiCu Inorganic materials 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
229910052770 Uranium Inorganic materials 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
239000011260 aqueous acid Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
239000011707 mineral Substances 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
150000003755 zirconium compounds Chemical class 0.000 description 1
DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/104—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/108—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/092—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings with aromatic radicals attached to the chain

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Hydrogenated Pyridines (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

NO162977A 1965-06-16 1966-05-11 NO119277B (da)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB25449/65A GB1111785A (en)	1965-06-16	1965-06-16	New piperazino-phenylethanol derivatives and process for preparing them

Publications (1)

Publication Number	Publication Date
NO119277B true NO119277B (da)	1970-04-27

Family

ID=10227858

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO162977A NO119277B (da)	1965-06-16	1966-05-11

Country Status (13)

Country	Link
US (1)	US3505334A (da)
AT (1)	AT261621B (da)
BE (1)	BE682206A (da)
BR (1)	BR6680468D0 (da)
CH (1)	CH463511A (da)
DE (1)	DE1620379A1 (da)
DK (1)	DK135234B (da)
ES (1)	ES327968A1 (da)
FR (1)	FR5977M (da)
GB (1)	GB1111785A (da)
NL (2)	NL6606392A (da)
NO (1)	NO119277B (da)
SE (1)	SE317082B (da)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3446808A (en) *	1964-05-25	1969-05-27	Universal Oil Prod Co	Borates of n-hydroxyalkyl-nitrogen-heterocyclic saturated compounds
JPS54130587A (en) *	1978-03-30	1979-10-09	Otsuka Pharmaceut Co Ltd	Carbostyryl derivative
ES8201575A1 (es) *	1980-11-24	1981-12-16	Ferrer Int	Procedimiento de obtencion de nuevos 2-aminoetanoles
JPS59101475A (ja) *	1982-12-02	1984-06-12	Nippon Chemiphar Co Ltd	新規ピペラジン誘導体およびその製造法ならびにこれを含有する脳循環改善剤
US4761415A (en) *	1986-08-28	1988-08-02	Smithkline Beckman Corporation	Dopamine-β-hydroxylase inhibitors
US4835154A (en) *	1987-06-01	1989-05-30	Smithkline Beckman Corporation	1-aralykyl-5-piperazinylmethyl-2-mercaptoimidazoles and 2-alkylthioimidazoles and their use as dopamine-βhydroxylase inhibitors
AUPN977296A0 (en) *	1996-05-10	1996-06-06	Monash University	Pharmaceutical agents
US6011035A (en) *	1998-06-30	2000-01-04	Neuromed Technologies Inc.	Calcium channel blockers

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2927924A (en) *	1958-04-03	1960-03-08	Lilly Co Eli	Novel phenethyl-substituted piperazines

0
- NL NL131192D patent/NL131192C/xx active
1965
- 1965-06-16 GB GB25449/65A patent/GB1111785A/en not_active Expired
1966
- 1966-05-10 NL NL6606392A patent/NL6606392A/xx unknown
- 1966-05-11 NO NO162977A patent/NO119277B/no unknown
- 1966-05-20 DK DK258766AA patent/DK135234B/da unknown
- 1966-05-24 CH CH745966A patent/CH463511A/fr unknown
- 1966-05-31 SE SE7431/66A patent/SE317082B/xx unknown
- 1966-06-02 US US554658A patent/US3505334A/en not_active Expired - Lifetime
- 1966-06-07 BE BE682206D patent/BE682206A/xx not_active IP Right Cessation
- 1966-06-15 ES ES0327968A patent/ES327968A1/es not_active Expired
- 1966-06-16 AT AT575866A patent/AT261621B/de active
- 1966-06-16 BR BR180468/66A patent/BR6680468D0/pt unknown
- 1966-06-16 DE DE19661620379 patent/DE1620379A1/de active Pending
- 1966-09-14 FR FR76351A patent/FR5977M/fr not_active Expired

Also Published As

Publication number	Publication date
SE317082B (da)	1969-11-10
AT261621B (de)	1968-05-10
DK135234B (da)	1977-03-21
NL131192C (da)
DK135234C (da)	1977-08-29
CH463511A (fr)	1968-10-15
NL6606392A (da)	1966-12-19
FR5977M (da)	1968-04-22
US3505334A (en)	1970-04-07
BR6680468D0 (pt)	1973-12-26
GB1111785A (en)	1968-05-01
BE682206A (da)	1966-12-07
DE1620379A1 (de)	1970-04-30
ES327968A1 (es)	1967-04-01

Publication	Publication Date	Title
US4298718A (en)	1981-11-03	Catalysts for the polymerization of olefins
US4006101A (en)	1977-02-01	Polymerization of olefins and catalysts therefor
US3454547A (en)	1969-07-08	Process for the preparation of polymerization catalysts
NO119277B (da)	1970-04-27
US3066130A (en)	1962-11-27	Process for finishing polyolefins
EP0067645A1 (en)	1982-12-22	Deactivation of catalyst in solution process for polymerization of alpha-olefins
US2915514A (en)	1959-12-01	Polymerization process
JPS5830887B2 (ja)	1983-07-02	高結晶性ポリオレフィンの精製方法
GB1576564A (en)	1980-10-08	Process for refining polypropylenes
US3931135A (en)	1976-01-06	Process for reusing polymerization solvent by recycling
US4167619A (en)	1979-09-11	Purification of propylene polymerization product
US3496156A (en)	1970-02-17	Process for purifying polyolefins
US3009907A (en)	1961-11-21	Recovery and purification of polyolefins
US2919264A (en)	1959-12-29	Process for removing catalyst residues from polyolefines
JPH0336841B2 (da)	1991-06-03
US3775389A (en)	1973-11-27	Process for the purification of polyolefins
JPH0348213B2 (da)	1991-07-23
CA1064010A (en)	1979-10-09	Process for the manufacture of a catalyst
US3287343A (en)	1966-11-22	Purification of polyolefins
US2928817A (en)	1960-03-15	Removal of metal contaminants in polymerization processes
US4332697A (en)	1982-06-01	Process for the preparation of catalyst component for the polymerization of α-olefins
SU445301A1 (ru)	1974-09-30	Способ получени полиолефинов
JPS5814447B2 (ja)	1983-03-19	塩化ビニルの重合方法
JPS5835525B2 (ja)	1983-08-03	ポリオレフィンの製造方法
US3127385A (en)	1964-03-31	Method of producing substantially