SU1034610A3 - Способ получени топливной смеси - Google Patents

Способ получени топливной смеси Download PDF

Info

Publication number: SU1034610A3
Authority: SU; USSR - Soviet Union
Prior art keywords: mixture; weight; ethanol; water; tert
Prior art date: 1980-03-31

Application number

SU813266251A

Other languages

English (en)

Russian (ru)

Inventor

Пескаролло Эрмано

Амчиллотти Франческо

Флорис Телемасо

Original Assignee

Снампрогетти С.П.А.(Фирма)

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.)

1980-03-31

Filing date

1981-03-30

Publication date

1983-08-07

1981-03-30 Application filed by Снампрогетти С.П.А.(Фирма) filed Critical Снампрогетти С.П.А.(Фирма)

1983-08-07 Application granted granted Critical

1983-08-07 Publication of SU1034610A3 publication Critical patent/SU1034610A3/ru

Links

239000000203 mixture Substances 0.000 title claims abstract description 78
239000000446 fuel Substances 0.000 title claims description 20
238000004519 manufacturing process Methods 0.000 title claims description 6
239000003054 catalyst Substances 0.000 claims abstract description 13
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 97
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 39
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 37
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 claims description 24
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 17
238000002955 isolation Methods 0.000 claims 1
150000001336 alkenes Chemical group 0.000 abstract description 11
238000000034 method Methods 0.000 abstract description 9
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract description 9
150000001298 alcohols Chemical class 0.000 abstract description 7
238000006243 chemical reaction Methods 0.000 abstract description 6
239000003456 ion exchange resin Substances 0.000 abstract description 4
229920003303 ion-exchange polymer Polymers 0.000 abstract description 4
230000002378 acidificating effect Effects 0.000 abstract 2
229910006069 SO3H Inorganic materials 0.000 abstract 1
230000003071 parasitic effect Effects 0.000 abstract 1
239000000376 reactant Substances 0.000 abstract 1
235000019441 ethanol Nutrition 0.000 description 41
239000000047 product Substances 0.000 description 28
238000004821 distillation Methods 0.000 description 15
239000007795 chemical reaction product Substances 0.000 description 12
150000002430 hydrocarbons Chemical class 0.000 description 10
229930195733 hydrocarbon Natural products 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
239000004215 Carbon black (E152) Substances 0.000 description 5
238000005194 fractionation Methods 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
-1 aliphatic alcohols Chemical class 0.000 description 4
239000007789 gas Substances 0.000 description 4
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
150000001768 cations Chemical class 0.000 description 3
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
229930195734 saturated hydrocarbon Natural products 0.000 description 3
MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Substances OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 2
238000002485 combustion reaction Methods 0.000 description 2
230000018044 dehydration Effects 0.000 description 2
238000006297 dehydration reaction Methods 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
230000036571 hydration Effects 0.000 description 2
238000006703 hydration reaction Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000004064 recycling Methods 0.000 description 2
238000000926 separation method Methods 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 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
235000002595 Solanum tuberosum Nutrition 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000003729 cation exchange resin Substances 0.000 description 1
229920001429 chelating resin Polymers 0.000 description 1
230000007423 decrease Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000004299 exfoliation Methods 0.000 description 1
238000000895 extractive distillation Methods 0.000 description 1
230000004907 flux Effects 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000002994 raw material Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
241000894007 species Species 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
239000013589 supplement Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
HVZJRWJGKQPSFL-UHFFFAOYSA-N tert-Amyl methyl ether Chemical compound CCC(C)(C)OC HVZJRWJGKQPSFL-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
- C07C29/80—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/03—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
- C07C29/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
- C12C11/00—Fermentation processes for beer
- C12C11/02—Pitching yeast

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Food Science & Technology (AREA)
Biochemistry (AREA)
Bioinformatics & Cheminformatics (AREA)
General Engineering & Computer Science (AREA)
Mycology (AREA)
Health & Medical Sciences (AREA)
Microbiology (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Liquid Carbonaceous Fuels (AREA)

SU813266251A 1980-03-31 1981-03-30 Способ получени топливной смеси SU1034610A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT21068/80A IT1140794B (it)	1980-03-31	1980-03-31	Procedimento per la produzione di alcoli c2-c4 "grado benzine" da miscele acquose che li contengono

Publications (1)

Publication Number	Publication Date
SU1034610A3 true SU1034610A3 (ru)	1983-08-07

Family

ID=11176255

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU813266251A SU1034610A3 (ru)	1980-03-31	1981-03-30	Способ получени топливной смеси

Country Status (25)

Country	Link
JP (1)	JPS56151790A (fr)
AU (1)	AU550088B2 (fr)
BE (1)	BE888150A (fr)
BR (1)	BR8101872A (fr)
CA (1)	CA1160252A (fr)
CH (1)	CH648340A5 (fr)
CS (1)	CS221292B2 (fr)
DD (1)	DD157700A5 (fr)
DE (1)	DE3112277C2 (fr)
DK (1)	DK137281A (fr)
ES (1)	ES501396A0 (fr)
FR (1)	FR2479186A1 (fr)
GB (1)	GB2072668B (fr)
HU (1)	HU192065B (fr)
IE (1)	IE51127B1 (fr)
IT (1)	IT1140794B (fr)
LU (1)	LU83265A1 (fr)
NL (1)	NL8101594A (fr)
NO (1)	NO811022L (fr)
NZ (1)	NZ196606A (fr)
PL (1)	PL230427A1 (fr)
RO (1)	RO84498B (fr)
SE (1)	SE8101977L (fr)
SU (1)	SU1034610A3 (fr)
YU (1)	YU41038B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0723331B2 (ja) *	1985-03-12	1995-03-15	旭化成工業株式会社	第３級ブタノ−ルの製造方法
US7007764B2 (en)	2002-12-06	2006-03-07	Manitowoc Crane Companies, Inc.	Carbody to crawler connection
JP2007021643A (ja) *	2005-07-15	2007-02-01	Amada Co Ltd	永久磁石を用いたワーク吸着装置
US10570071B1 (en)	2018-12-12	2020-02-25	Saudi Arabian Oil Company	Membrane-based process for butanols production from mixed butenes

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL299568A (fr) *		1900-01-01
FR1314120A (fr) *	1962-01-08	1963-01-04	Bayer Ag	Procédé de préparation d'éthers de tert.-butyle et d'alcoyles
DE1249844B (de) *	1962-03-21	1967-09-14	GuIf Research &. Development Company, Pittsburgh, Pa (V St A)	Verfahren zur Herstellung von Alkoholen durch Anlagerung von Wasser an die entsprechenden Olefine m flussiger Phase
US3822119A (en) *	1970-11-19	1974-07-02	Goodyear Tire & Rubber	Anti-pollution anti-knock gasoline
DE2629769C3 (de) *	1976-07-02	1989-03-16	Hüls AG, 4370 Marl	Verfahren zur Herstellung von reinem Methyl-tertiär-butyläther
US4087471A (en) *	1977-05-20	1978-05-02	Petro-Tex Chemical Corporation	Fixed bed process for the production of t-butanol

1980
- 1980-03-31 IT IT21068/80A patent/IT1140794B/it active
1981
- 1981-03-18 IE IE602/81A patent/IE51127B1/en unknown
- 1981-03-19 GB GB8108640A patent/GB2072668B/en not_active Expired
- 1981-03-24 NZ NZ196606A patent/NZ196606A/en unknown
- 1981-03-26 BR BR8101872A patent/BR8101872A/pt unknown
- 1981-03-26 NO NO811022A patent/NO811022L/no unknown
- 1981-03-26 DK DK137281A patent/DK137281A/da not_active Application Discontinuation
- 1981-03-26 FR FR8106118A patent/FR2479186A1/fr active Granted
- 1981-03-27 DE DE3112277A patent/DE3112277C2/de not_active Expired
- 1981-03-27 SE SE8101977A patent/SE8101977L/xx not_active Application Discontinuation
- 1981-03-27 BE BE0/204278A patent/BE888150A/fr not_active IP Right Cessation
- 1981-03-30 JP JP4566881A patent/JPS56151790A/ja active Pending
- 1981-03-30 RO RO103858A patent/RO84498B/ro unknown
- 1981-03-30 AU AU68903/81A patent/AU550088B2/en not_active Ceased
- 1981-03-30 PL PL23042781A patent/PL230427A1/xx unknown
- 1981-03-30 HU HU81810A patent/HU192065B/hu unknown
- 1981-03-30 YU YU828/81A patent/YU41038B/xx unknown
- 1981-03-30 LU LU83265A patent/LU83265A1/fr unknown
- 1981-03-30 CH CH2146/81A patent/CH648340A5/it not_active IP Right Cessation
- 1981-03-30 SU SU813266251A patent/SU1034610A3/ru active
- 1981-03-30 CA CA000374128A patent/CA1160252A/fr not_active Expired
- 1981-03-31 CS CS812393A patent/CS221292B2/cs unknown
- 1981-03-31 NL NL8101594A patent/NL8101594A/nl not_active Application Discontinuation
- 1981-03-31 DD DD81228774A patent/DD157700A5/de unknown
- 1981-03-31 ES ES501396A patent/ES501396A0/es active Granted

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
1. Расширение энергетическихресурсов и снижение загр зненности атмосферл за счет использовани спиртового топлива метил .. Dni I (:)tae) , 1974, 21, Н 11, с.19-21, 2,SAE Pvept- .,S.a. № 750120, 1975 с.27. 3.За вка GB №2010323 кл. С 10 V. 1/18, опуЪлик. 1979. 4..Нестабильность метильно-бензиновых смесей.- ABcVie .Seh , 1977, 73, № 165, с.312-318. 5.Кратка химическа энциклопеди . Т.5, с.1042-1051. 6. «te m . Еио-. , 1972, 17, №9, 10-12-1016.. 7.Коган В. Б. Азоотропна и экстрактивна ректификаци . Хими , 1971, с.401. *

Also Published As

Publication number	Publication date
NL8101594A (nl)	1981-10-16
RO84498A (fr)	1984-06-21
IE51127B1 (en)	1986-10-15
IT8021068A0 (it)	1980-03-31
NO811022L (no)	1981-10-01
YU82881A (en)	1983-02-28
PL230427A1 (fr)	1981-11-13
DD157700A5 (de)	1982-12-01
GB2072668A (en)	1981-10-07
DK137281A (da)	1981-10-01
DE3112277A1 (de)	1982-03-18
DE3112277C2 (de)	1985-05-02
RO84498B (ro)	1984-08-30
YU41038B (en)	1986-10-31
SE8101977L (sv)	1981-10-01
AU550088B2 (en)	1986-03-06
BR8101872A (pt)	1981-10-06
LU83265A1 (fr)	1981-10-29
FR2479186B1 (fr)	1982-11-26
CA1160252A (fr)	1984-01-10
IE810602L (en)	1981-09-30
JPS56151790A (en)	1981-11-24
GB2072668B (en)	1984-03-28
CS221292B2 (en)	1983-04-29
CH648340A5 (it)	1985-03-15
HU192065B (en)	1987-05-28
ES8202776A1 (es)	1982-02-16
AU6890381A (en)	1981-10-08
NZ196606A (en)	1984-03-16
FR2479186A1 (fr)	1981-10-02
IT1140794B (it)	1986-10-10
BE888150A (fr)	1981-09-28
ES501396A0 (es)	1982-02-16

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