DD140050A5 - Verfahren zur herstellung harzartiger polyolefine - Google Patents

Verfahren zur herstellung harzartiger polyolefine Download PDF

Info

Publication number: DD140050A5
Authority: DD; German Democratic Republic
Prior art keywords: item; titanium catalyst; catalyst component; high yield; olefin
Prior art date: 1977-11-25

Application number

DD78209306A

Other languages

German (de)

English (en)

Inventor

Glen R Hoff

John L Melquist

Peter Fotis

Original Assignee

Standard Oil Co

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.)

1977-11-25

Filing date

1978-11-24

Publication date

1980-02-06

1978-11-24 Application filed by Standard Oil Co filed Critical Standard Oil Co

1980-02-06 Publication of DD140050A5 publication Critical patent/DD140050A5/de

Links

238000004519 manufacturing process Methods 0.000 title description 9
239000003054 catalyst Substances 0.000 claims description 151
239000007788 liquid Substances 0.000 claims description 75
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 57
229910052719 titanium Inorganic materials 0.000 claims description 57
239000010936 titanium Substances 0.000 claims description 57
238000010791 quenching Methods 0.000 claims description 54
239000012808 vapor phase Substances 0.000 claims description 53
-1 hydride groups Chemical group 0.000 claims description 50
238000000034 method Methods 0.000 claims description 47
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 44
238000006116 polymerization reaction Methods 0.000 claims description 41
150000001336 alkenes Chemical class 0.000 claims description 30
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 24
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 24
125000000217 alkyl group Chemical group 0.000 claims description 20
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 18
239000005977 Ethylene Substances 0.000 claims description 18
230000008569 process Effects 0.000 claims description 18
230000000171 quenching effect Effects 0.000 claims description 16
229910052751 metal Inorganic materials 0.000 claims description 15
239000002184 metal Substances 0.000 claims description 15
239000000203 mixture Substances 0.000 claims description 15
238000002360 preparation method Methods 0.000 claims description 15
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 13
239000003638 chemical reducing agent Substances 0.000 claims description 11
229920000098 polyolefin Polymers 0.000 claims description 11
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 10
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
239000001301 oxygen Substances 0.000 claims description 9
229910052760 oxygen Inorganic materials 0.000 claims description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 7
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 7
229910000041 hydrogen chloride Inorganic materials 0.000 claims description 7
150000001335 aliphatic alkanes Chemical class 0.000 claims description 6
238000012685 gas phase polymerization Methods 0.000 claims description 2
VPUGDVKSAQVFFS-UHFFFAOYSA-N coronene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3)C4=C4C3=CC=C(C=C3)C4=C2C3=C1 VPUGDVKSAQVFFS-UHFFFAOYSA-N 0.000 claims 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 47
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 38
229920000642 polymer Polymers 0.000 description 27
229910052782 aluminium Inorganic materials 0.000 description 24
239000001282 iso-butane Substances 0.000 description 19
239000001257 hydrogen Substances 0.000 description 17
229910052739 hydrogen Inorganic materials 0.000 description 17
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 15
125000004432 carbon atom Chemical group C* 0.000 description 13
238000002156 mixing Methods 0.000 description 13
239000000178 monomer Substances 0.000 description 12
239000000463 material Substances 0.000 description 11
239000003795 chemical substances by application Substances 0.000 description 10
229910052723 transition metal Inorganic materials 0.000 description 9
150000003624 transition metals Chemical class 0.000 description 9
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
239000003085 diluting agent Substances 0.000 description 8
239000000243 solution Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
150000001805 chlorine compounds Chemical class 0.000 description 7
150000002681 magnesium compounds Chemical class 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
230000000415 inactivating effect Effects 0.000 description 6
QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 6
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
229920000573 polyethylene Polymers 0.000 description 6
239000004698 Polyethylene Substances 0.000 description 5
150000001298 alcohols Chemical class 0.000 description 5
150000001299 aldehydes Chemical class 0.000 description 5
150000002170 ethers Chemical class 0.000 description 5
239000007789 gas Substances 0.000 description 5
150000004820 halides Chemical class 0.000 description 5
229910052749 magnesium Inorganic materials 0.000 description 5
239000011777 magnesium Substances 0.000 description 5
239000000047 product Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
150000001735 carboxylic acids Chemical class 0.000 description 4
150000002431 hydrogen Chemical class 0.000 description 4
230000002779 inactivation Effects 0.000 description 4
150000002576 ketones Chemical class 0.000 description 4
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
239000007787 solid Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
150000003609 titanium compounds Chemical class 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
230000009849 deactivation Effects 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 3
238000009826 distribution Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 3
150000004678 hydrides Chemical group 0.000 description 3
150000002894 organic compounds Chemical class 0.000 description 3
XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-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
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
239000006228 supernatant Substances 0.000 description 3
150000003623 transition metal compounds Chemical class 0.000 description 3
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical group CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
150000004703 alkoxides Chemical class 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000005234 alkyl aluminium group Chemical group 0.000 description 2
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
230000000903 blocking effect Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 2
239000001273 butane Substances 0.000 description 2
WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 2
150000001733 carboxylic acid esters Chemical class 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000007865 diluting Methods 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
150000002019 disulfides Chemical class 0.000 description 2
DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
239000003701 inert diluent Substances 0.000 description 2
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000002808 molecular sieve Substances 0.000 description 2
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 2
BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
239000011949 solid catalyst Substances 0.000 description 2
150000003608 titanium Chemical class 0.000 description 2
LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical group CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 1
LOXRGHGHQYWXJK-UHFFFAOYSA-N 1-octylsulfanyloctane Chemical compound CCCCCCCCSCCCCCCCC LOXRGHGHQYWXJK-UHFFFAOYSA-N 0.000 description 1
QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical class CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
RVDLHGSZWAELAU-UHFFFAOYSA-N 5-tert-butylthiophene-2-carbonyl chloride Chemical compound CC(C)(C)C1=CC=C(C(Cl)=O)S1 RVDLHGSZWAELAU-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
244000287680 Garcinia dulcis Species 0.000 description 1
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical group CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
239000012346 acetyl chloride Substances 0.000 description 1
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 1
230000004913 activation Effects 0.000 description 1
150000001266 acyl halides Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000003934 aromatic aldehydes Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
230000008901 benefit Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 description 1
239000000969 carrier Substances 0.000 description 1
238000005266 casting Methods 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
229910000423 chromium oxide Inorganic materials 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
150000003997 cyclic ketones Chemical class 0.000 description 1
150000001924 cycloalkanes Chemical class 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical compound CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
235000012489 doughnuts Nutrition 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
WLPSNBGDESCKIL-UHFFFAOYSA-N ethanol;titanium Chemical compound [Ti].CCO WLPSNBGDESCKIL-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical class CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical group CCCCCCO ZSIAUFGUXNUGDI-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
BICAGYDGRXJYGD-UHFFFAOYSA-N hydrobromide;hydrochloride Chemical compound Cl.Br BICAGYDGRXJYGD-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000011031 large-scale manufacturing process Methods 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
159000000003 magnesium salts Chemical class 0.000 description 1
XDKQUSKHRIUJEO-UHFFFAOYSA-N magnesium;ethanolate Chemical compound [Mg+2].CC[O-].CC[O-] XDKQUSKHRIUJEO-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
239000002574 poison Substances 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
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230000000379 polymerizing effect Effects 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000001294 propane Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000000523 sample Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
230000000153 supplemental effect Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
PSDQQCXQSWHCRN-UHFFFAOYSA-N vanadium(4+) Chemical compound [V+4] PSDQQCXQSWHCRN-UHFFFAOYSA-N 0.000 description 1
238000009834 vaporization Methods 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
239000012991 xanthate Substances 0.000 description 1
229910052726 zirconium Inorganic materials 0.000 description 1
150000003755 zirconium compounds Chemical class 0.000 description 1
GBNDTYKAOXLLID-UHFFFAOYSA-N zirconium(4+) ion Chemical compound [Zr+4] GBNDTYKAOXLLID-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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/18—Stationary reactors having moving elements inside
- B01J19/1868—Stationary reactors having moving elements inside resulting in a loop-type movement
- B01J19/1881—Stationary reactors having moving elements inside resulting in a loop-type movement externally, i.e. the mixture leaving the vessel and subsequently re-entering it
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/08—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles
- B01J8/10—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles moved by stirrers or by rotary drums or rotary receptacles or endless belts
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
- B01J8/36—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed through which there is an essentially horizontal flow of particles
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
- B01J8/38—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed containing a rotatable device or being subject to rotation or to a circulatory movement, i.e. leaving a vessel and subsequently re-entering it
- B01J8/382—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed containing a rotatable device or being subject to rotation or to a circulatory movement, i.e. leaving a vessel and subsequently re-entering it with a rotatable device only
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/18—Details relating to the spatial orientation of the reactor
- B01J2219/182—Details relating to the spatial orientation of the reactor horizontal
- 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
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/08—Presence of a deactivator
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
- 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
- Y10S526/901—Monomer polymerized in vapor state in presence of transition metal containing catalyst

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Combustion & Propulsion (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Polymerisation Methods In General (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

DD78209306A 1977-11-25 1978-11-24 Verfahren zur herstellung harzartiger polyolefine DD140050A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/854,831 US4130699A (en)	1977-11-25	1977-11-25	Vapor phase polymerization with temporarily inactive titanium catalyst

Publications (1)

Publication Number	Publication Date
DD140050A5 true DD140050A5 (de)	1980-02-06

Family

ID=25319628

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD78209306A DD140050A5 (de)	1977-11-25	1978-11-24	Verfahren zur herstellung harzartiger polyolefine

Country Status (17)

Country	Link
US (1)	US4130699A (cs)
JP (1)	JPS5483084A (cs)
AT (1)	AT367774B (cs)
BE (1)	BE872247A (cs)
BR (1)	BR7807718A (cs)
CA (1)	CA1103396A (cs)
CS (1)	CS214856B2 (cs)
DD (1)	DD140050A5 (cs)
DE (1)	DE2850335A1 (cs)
FR (1)	FR2410007A1 (cs)
GB (1)	GB2008597B (cs)
IN (1)	IN150336B (cs)
IT (1)	IT1107674B (cs)
MX (1)	MX149390A (cs)
NL (1)	NL185012C (cs)
PL (1)	PL114316B1 (cs)
YU (1)	YU272978A (cs)

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USRE30148E (en) *	1974-12-16	1979-11-13	Standard Oil Company (Indiana)	Melt finishing process for polymers produced by vapor state polymerization processes
DE2966150D1 (en) *	1978-03-23	1983-10-20	Ici Plc	Gas-phase olefin polymerisation system and process for operating it
DE2841715A1 (de) *	1978-09-25	1980-04-10	Basf Ag	Verfahren zum herstellen von homo- und copolymerisaten von alpha -monoolefinen
US4210559A (en) *	1978-10-30	1980-07-01	Standard Oil Company (Indiana)	Catalyst for the preparation of polyalpha-olefins having broad molecular weight distributions
US4233182A (en) *	1978-12-26	1980-11-11	Standard Oil Company (Indiana)	High activity catalyst for the polymerization of alpha-olefins
US4313850A (en) *	1979-10-15	1982-02-02	Standard Oil Company (Indiana)	Catalyst for the polymerization of alpha-olefins
US4324691A (en) *	1980-01-10	1982-04-13	Imperial Chemical Industries Limited	Catalyst component
US4325835A (en) *	1980-01-10	1982-04-20	Imperial Chemical Industries Limited	Catalyst component
JPS56159205A (en) *	1980-05-14	1981-12-08	Nippon Oil Co Ltd	Equipment for olefin gas-phase polymerization
JPS56129204A (en) *	1980-03-14	1981-10-09	Nippon Oil Co Ltd	Apparatus for vapor-phase polymerization of olefin
US4326048A (en) *	1980-05-27	1982-04-20	Standard Oil Company (Indiana)	Method for emergency shutdown of gas phase polyolefin reactor
US4311612A (en) *	1980-08-25	1982-01-19	Standard Oil Company (Indiana)	Olefin polymerization catalyst
US4287327A (en) *	1980-09-29	1981-09-01	Standard Oil Company (Indiana)	Process for controlling polymer particle size in vapor phase polymerization
JPS581708A (ja) *	1981-06-25	1983-01-07	Mitsubishi Chem Ind Ltd	ポリオレフインの製造法
US4446288A (en) *	1981-05-05	1984-05-01	Chemplex Company	Polymerization method
US4402861A (en) *	1981-05-05	1983-09-06	Chemplex Company	Polymerization catalyst and method
US4384983A (en) *	1981-05-26	1983-05-24	Standard Oil Company (Indiana)	Catalyst and process for production of polyolefins of improved morphology
US4376064A (en) *	1981-05-26	1983-03-08	Standard Oil Co. (Indiana)	Catalyst and process for production of polyolefins of improved morphology
US4374753A (en) *	1981-07-29	1983-02-22	Chemplex Company	Polymerization catalyst and method
US4478988A (en) *	1981-07-29	1984-10-23	Chemplex Company	Polymerization method
US4407727A (en) *	1982-10-08	1983-10-04	Atlantic Richfield Company	Method of supporting a catalyst on polyolefins
FR2566781B1 (fr) *	1984-06-28	1986-11-14	Bp Chimie Sa	Procede de polymerisation ou de copolymerisation d'alpha-olefines en lit fluidise, en presence d'un systeme catalytique ziegler-natta
US4634744A (en) *	1985-01-09	1987-01-06	Chemplex Company	Method of catalyst deactivation
FR2588559B1 (fr) *	1985-10-11	1988-03-11	Bp Chimie Sa	Procede de polymerisation ou de copolymerisation d'alpha-olefines en presence d'un systeme catalytique ziegler-natta ameliore
US4921919A (en) *	1985-12-10	1990-05-01	Amoco Corporation	Method and apparatus for minimizing polymer agglomerate or lump formation in a gas-phase polypropylene polymerization reactor
US4855370A (en) *	1986-10-01	1989-08-08	Union Carbide Corporation	Method for reducing sheeting during polymerization of alpha-olefins
IT1227240B (it) *	1988-09-29	1991-03-27	Enichem Anic Spa	Procedimento per la polimerizzazione dell'etilene e perla copolimerizzazione dell'etilene con alfa-olefine e catalizzatore relativo
JP2850427B2 (ja) *	1989-12-25	1999-01-27	東ソー株式会社	ポリオレフィンの製造方法
JP2952695B2 (ja) *	1990-09-04	1999-09-27	東ソー株式会社	立体規則性ポリオレフィンの製造方法
DE4130353A1 (de) *	1991-09-12	1993-03-18	Basf Ag	Verfahren zur herstellung von ziegler-natta-katalysatorsystemen
US5151397A (en) *	1991-12-16	1992-09-29	Phillips Petroleum Company	Method of producing metal halide catalyst
ES2188210T3 (es) *	1998-08-10	2003-06-16	Bp Chem Int Ltd	Procedimiento continuo para el revestimiento en fase gaseosa de un catalizador de polimerizacion.
NL1010294C2 (nl) *	1998-10-12	2000-04-13	Dsm Nv	Werkwijze en inrichting voor de bereiding van een olefine-polymeer.
JP5484290B2 (ja) *	2009-11-06	2014-05-07	日本ポリプロ株式会社	プロピレン重合反応装置及びプロピレン系ブロック共重合体の製造方法
US9243138B2 (en)	2011-03-18	2016-01-26	Ineos Manufacturing Belgium Nv	Propylene-ethylene random copolymer
WO2014118149A1 (en)	2013-01-29	2014-08-07	Ineos Europe Ag	Injection moulded polypropylene articles
MX2024009353A (es)	2022-02-03	2024-09-30	Ineos Europe Ag	Mezcla de poliolefina que contiene aluminio reciclado.

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US3002963A (en) *	1957-04-22	1961-10-03	Phillips Petroleum Co	Gas phase polymerization utilizing a free-settling, fluidized catalyst and reactor system therefor
US3023203A (en) *	1957-08-16	1962-02-27	Phillips Petroleum Co	Polymerization process
US3676415A (en) *	1968-06-27	1972-07-11	Hoechst Ag	Process for polymerizing {60 -olefins
US3644318A (en) *	1968-08-21	1972-02-22	Hoechst Ag	Process for the polymerization of olefins
DE1795268A1 (de) *	1968-08-30	1972-07-27	Hoechst Ag	Verfahren zur Polymerisation von Olefinen
DE1805765C3 (de) *	1968-10-29	1980-09-11	Basf Ag, 6700 Ludwigshafen	Verfahren zur Polymerisation von Propylen
DE2001183C3 (de) *	1970-01-13	1980-01-31	Chemische Werke Huels Ag, 4370 Marl	Verfahren zur Unterbrechung und Wiederingangsetzung von Olefinpolymerisationen
US3971768A (en) *	1974-12-16	1976-07-27	Standard Oil Company (Indiana)	Vapor phase reactor off-gas recycle system for use in the vapor state polymerization of monomers
US3957448A (en) *	1974-12-16	1976-05-18	Standard Oil Company	Divided horizontal reactor for the vapor phase polymerization of monomers at different hydrogen levels
US3965083A (en) *	1974-12-16	1976-06-22	Standard Oil Company	Process for the vapor phase polymerization of monomers in a horizontal, quench-cooled, stirred-bed reactor using essentially total off-gas recycle and melt finishing
IN145649B (cs) *	1974-12-16	1985-01-05	Standard Oil Co
FR2312512A1 (fr) *	1975-05-27	1976-12-24	Naphtachimie Sa	Procede de polymerisation des olefines en lit fluidise
LU76170A1 (cs) *	1975-11-14	1977-06-03

1977
- 1977-11-25 US US05/854,831 patent/US4130699A/en not_active Expired - Lifetime
1978
- 1978-10-31 CA CA315,289A patent/CA1103396A/en not_active Expired
- 1978-11-02 IN IN788/DEL/78A patent/IN150336B/en unknown
- 1978-11-07 NL NLAANVRAGE7811060,A patent/NL185012C/xx not_active IP Right Cessation
- 1978-11-17 MX MX175673A patent/MX149390A/es unknown
- 1978-11-20 DE DE19782850335 patent/DE2850335A1/de not_active Withdrawn
- 1978-11-22 GB GB7845582A patent/GB2008597B/en not_active Expired
- 1978-11-22 YU YU02729/78A patent/YU272978A/xx unknown
- 1978-11-23 BE BE191913A patent/BE872247A/xx not_active IP Right Cessation
- 1978-11-23 BR BR7807718A patent/BR7807718A/pt unknown
- 1978-11-24 IT IT52068/78A patent/IT1107674B/it active
- 1978-11-24 FR FR7833335A patent/FR2410007A1/fr active Granted
- 1978-11-24 DD DD78209306A patent/DD140050A5/de unknown
- 1978-11-24 JP JP14520278A patent/JPS5483084A/ja active Granted
- 1978-11-25 PL PL1978211226A patent/PL114316B1/pl unknown
- 1978-11-27 AT AT0847478A patent/AT367774B/de not_active IP Right Cessation
- 1978-11-27 CS CS787772A patent/CS214856B2/cs unknown

Also Published As

Publication number	Publication date
MX149390A (es)	1983-11-01
IT1107674B (it)	1985-11-25
AT367774B (de)	1982-07-26
IT7852068A0 (it)	1978-11-24
NL7811060A (nl)	1979-05-29
IN150336B (cs)	1982-09-11
GB2008597A (en)	1979-06-06
PL211226A1 (pl)	1979-08-27
GB2008597B (en)	1982-06-30
YU272978A (en)	1982-06-30
FR2410007B1 (cs)	1981-01-16
JPS641483B2 (cs)	1989-01-11
BE872247A (fr)	1979-05-23
PL114316B1 (en)	1981-01-31
CA1103396A (en)	1981-06-16
BR7807718A (pt)	1979-07-31
ATA847478A (de)	1981-12-15
NL185012B (nl)	1989-08-01
NL185012C (nl)	1990-01-02
CS214856B2 (en)	1982-06-25
US4130699A (en)	1978-12-19
JPS5483084A (en)	1979-07-02
FR2410007A1 (fr)	1979-06-22
DE2850335A1 (de)	1979-05-31

Publication	Publication Date	Title
DE2850335A1 (de)	1979-05-31	Verfahren zur herstellung harzartiger polyolefine
DE2146685C3 (de)	1987-02-12	Verfahren zur Polymerisation von Äthylen und Katalysator zur Durchführung dieses Verfahrens
DE1420648A1 (de)	1968-12-12	Verfahren und Katalysator zur Herstellung von Olefinpolymeren
DE2522331A1 (de)	1975-12-04	Katalysator zum polymerisieren oder copolymerisieren von olefinen sowie dessen herstellung und verwendung
EP0264895A2 (de)	1988-04-27	Verfahren zum Herstellen von Homo- sowie Copolymerisaten des Ethens durch Phillips-Katalysator
DE2159910A1 (de)	1972-06-15	Verfahren zum Polymerisieren von Alkylenen
DE10392773T5 (de)	2005-08-04	Eine feste Katalysatorkomponente für die Polymerisation von Ethylen, Herstellung derselben und ein Katalysator diese enthaltend
DE1620927A1 (de)	1970-09-24	Verfahren zur Herstellung von hohem cis-1,4-Polybutadien
DE1520900C3 (de)	1978-07-13	Verfahren zum Polymerisieren von Olefinen
DE1520792A1 (de)	1970-01-22	Verfahren zur Polymerisation von Olefinen
DE1294655B (de)	1969-05-08	Verfahren zur Herstellung von Polyolefinen
DE1443798B2 (de)	1976-12-02	Verfahren zur gewinnung von gesaettigten aliphatischen carbonsaeuren
CH462148A (de)	1968-09-15	Verfahren zur Herstellung von Zyklododekatrienen-1,5,9
DE2441625A1 (de)	1975-03-20	Verfahren zur niederdruckpolymerisation von alpha-olefinen
DE1958585B2 (de)	1978-09-21	Verfahren zur Herstellung von Äthylenhomopolymerisaten oder -copolymerisaten mit a-Olefinen
AT222351B (de)	1962-07-25	Verfahren zur Herstellung von unter Normalbedingungen festen Äthylenpolymeren
DE3346798A1 (de)	1984-08-02	Verfahren zur herstellung von polyolefinen
DE2400582C3 (de)	1979-09-13	Verfahren zur Herstellung von Buten-(l)
DE2142356A1 (de)	1972-03-02	Verfahren zur Gewinnung eines Produk tes mit überwiegendem Gehalt an geradket tigen alpha Olefinen aus athanhaltigem Äthylen
DE69805980T2 (de)	2003-01-23	Verfahren zur herstellung von carbonsäuren
DE1645284A1 (de)	1970-05-14	Verfahren zur Herstellung von Polyolefinprodukten
DE69304667T2 (de)	1997-01-23	Verfahren zur Herstellung von linearen alpha-Olefinen mittels einer geänderten Kettenwachsverfahren
DE1443624A1 (de)	1969-02-13	Verfahren zur katalytischen Herstellung von 1,5,9-Cyclododecatrienen
DE1443798C3 (de)	1977-07-28	Verfahren zur Gewinnung von gesättigten aliphatischen Carbonsäuren
DE1720386A1 (de)	1972-03-30	Verfahren zur Polymerisation organischer Monomere