CS235404B1 - Způsob zpracování C,-frakce odpadající z výroby methyl-terc.butyl-etheru - Google Patents

Způsob zpracování C,-frakce odpadající z výroby methyl-terc.butyl-etheru Download PDF

Info

Publication number: CS235404B1
Authority: CS; Czechoslovakia
Prior art keywords: polymerization; alcl; catalyst; butene; methyl
Prior art date: 1983-01-28

Application number

CS57483A

Other languages

Czech (cs)

English (en)

Inventor

Miroslav Marek

Vlastimil Halaska

Jiri Mostecky

Original Assignee

Miroslav Marek

Vlastimil Halaska

Jiri Mostecky

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.)

1983-01-28

Filing date

1983-01-28

Publication date

1985-05-15

1983-01-28 Application filed by Miroslav Marek, Vlastimil Halaska, Jiri Mostecky filed Critical Miroslav Marek

1983-01-28 Priority to CS57483A priority Critical patent/CS235404B1/sk

1985-05-15 Publication of CS235404B1 publication Critical patent/CS235404B1/sk

Links

BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 title claims description 11
238000000034 method Methods 0.000 title claims description 9
238000004519 manufacturing process Methods 0.000 title claims description 5
239000003054 catalyst Substances 0.000 claims description 17
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
VXNZUUAINFGPBY-UHFFFAOYSA-N ethyl ethylene Natural products CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 14
229920001083 polybutene Polymers 0.000 claims description 6
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 4
IAQRGUVFOMOMEM-ARJAWSKDSA-N cis-but-2-ene Chemical compound C\C=C/C IAQRGUVFOMOMEM-ARJAWSKDSA-N 0.000 claims description 4
IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 claims description 4
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 3
230000003197 catalytic effect Effects 0.000 claims description 2
239000011951 cationic catalyst Substances 0.000 claims description 2
238000007334 copolymerization reaction Methods 0.000 claims description 2
238000006116 polymerization reaction Methods 0.000 description 28
239000003921 oil Substances 0.000 description 12
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 11
239000000725 suspension Substances 0.000 description 10
239000011541 reaction mixture Substances 0.000 description 9
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
239000000243 solution Substances 0.000 description 6
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
238000007792 addition Methods 0.000 description 4
238000000227 grinding Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
229920002367 Polyisobutene Polymers 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 3
238000001816 cooling Methods 0.000 description 3
229960003750 ethyl chloride Drugs 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
239000000203 mixture Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
239000004215 Carbon black (E152) Substances 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
239000005662 Paraffin oil Substances 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
ZTHNOZQGTXKVNZ-UHFFFAOYSA-L dichloroaluminum Chemical compound Cl[Al]Cl ZTHNOZQGTXKVNZ-UHFFFAOYSA-L 0.000 description 2
150000008282 halocarbons Chemical class 0.000 description 2
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
238000002955 isolation Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical class [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
239000002002 slurry Substances 0.000 description 2
NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 description 2
239000003039 volatile agent Substances 0.000 description 2
UKDOTCFNLHHKOF-FGRDZWBJSA-N (z)-1-chloroprop-1-ene;(z)-1,2-dichloroethene Chemical group C\C=C/Cl.Cl\C=C/Cl UKDOTCFNLHHKOF-FGRDZWBJSA-N 0.000 description 1
101100108644 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) alo-1 gene Proteins 0.000 description 1
229930182555 Penicillin Natural products 0.000 description 1
JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical class CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
239000012346 acetyl chloride Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
238000010538 cationic polymerization reaction Methods 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000012230 colorless oil Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
201000006549 dyspepsia Diseases 0.000 description 1
230000000694 effects Effects 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000011049 filling Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
208000024798 heartburn Diseases 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
239000003999 initiator Substances 0.000 description 1
239000001282 iso-butane Substances 0.000 description 1
229940050176 methyl chloride Drugs 0.000 description 1
238000003801 milling Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
229940049954 penicillin Drugs 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000001294 propane Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
208000024981 pyrosis Diseases 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000012047 saturated solution Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000010689 synthetic lubricating oil Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Landscapes

Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

CS57483A 1983-01-28 1983-01-28 Způsob zpracování C,-frakce odpadající z výroby methyl-terc.butyl-etheru CS235404B1 (sk)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CS57483A CS235404B1 (sk)	1983-01-28	1983-01-28	Způsob zpracování C,-frakce odpadající z výroby methyl-terc.butyl-etheru

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CS57483A CS235404B1 (sk)	1983-01-28	1983-01-28	Způsob zpracování C,-frakce odpadající z výroby methyl-terc.butyl-etheru

Publications (1)

Publication Number	Publication Date
CS235404B1 true CS235404B1 (sk)	1985-05-15

Family

ID=5338064

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS57483A CS235404B1 (sk)	1983-01-28	1983-01-28	Způsob zpracování C,-frakce odpadající z výroby methyl-terc.butyl-etheru

Country Status (1)

Country	Link
CS (1)	CS235404B1 (sk)

1983
- 1983-01-28 CS CS57483A patent/CS235404B1/sk unknown

Publication	Publication Date	Title
EP0558187B1 (en)	1996-04-10	Butene polymers
SU784785A3 (ru)	1980-11-30	Способ получени полиолефинов
CA2159479A1 (en)	1995-08-17	Ionic liquids
NO140949B (no)	1979-09-03	Anordning for tilveiebringelse av et signal representativt for bormoment
US4558170A (en)	1985-12-10	Polyisobutylene process
US2315080A (en)	1943-03-30	Process for manufacture of viscous polymers
US4306105A (en)	1981-12-15	Process for the production of polyisobutenes
EP0337737B1 (en)	1995-07-05	Method for producing "poly-N-butene oils" from C4-fraction residues
CS235404B1 (sk)	1985-05-15	Způsob zpracování C,-frakce odpadající z výroby methyl-terc.butyl-etheru
US5012030A (en)	1991-04-30	Process for preparing polybutenes with increased reactivity
US3398131A (en)	1968-08-20	Homopolymerization of ethylene for the production of solid and liquid polymers
EP0324838B1 (en)	1993-05-12	Lower alkene polymers
CA1283997C (en)	1991-05-07	Fixed bed process for polymerizing liquid butenes
US4642410A (en)	1987-02-10	Catalytic poly alpha-olefin process
US3737477A (en)	1973-06-05	Process of preparing ethylene propylene copolymer oils
EP0752913B1 (en)	1999-04-21	Supported lewis acid catalysts for hydrocarbon conversion reactions
EP0101205A2 (en)	1984-02-22	Process for preparing polyisobutylene
US3851011A (en)	1974-11-26	Ethylene-propylene copolymer oil preparation using vanadium-aluminum catalyst
US3950453A (en)	1976-04-13	Process for preparing petroleum resins
US2571354A (en)	1951-10-16	Polymerization of monoalkylethylenes
US4532061A (en)	1985-07-30	Grafted polyalphaolefin polymers, method for its production and oils containing it
NO134089B (sk)	1976-05-03
NO116048B (sk)	1969-01-20
US2882289A (en)	1959-04-14	Alkylation process and catalyst therefor
CZ173795A3 (en)	1995-12-13	Process for preparing synthetic oils, olefinic copolymer for such oils and process for preparing thereof