SE451545B - Katalytiskt system och framstellning av blandningar av metanol och hogre alkoholer med anvendning av systemet - Google Patents

Katalytiskt system och framstellning av blandningar av metanol och hogre alkoholer med anvendning av systemet

Info

Publication number: SE451545B
Authority: SE; Sweden
Prior art keywords: metals; catalyst; catalytic system; alkali; methanol
Prior art date: 1981-12-02

Application number

SE8206257A

Other languages

English (en)

Swedish (sv)

Other versions

SE8206257D0 (sv

SE8206257L (sv

Inventor

V Fattore

B Notari

A Paggini

V Lagana

Original Assignee

Snam Progetti

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.)

1981-12-02

Filing date

1982-11-03

Publication date

1987-10-19

1982-11-03 Application filed by Snam Progetti filed Critical Snam Progetti

1982-11-03 Publication of SE8206257D0 publication Critical patent/SE8206257D0/xx

1983-06-03 Publication of SE8206257L publication Critical patent/SE8206257L/

1987-10-19 Publication of SE451545B publication Critical patent/SE451545B/sv

Links

239000000203 mixture Substances 0.000 title claims description 20
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 title claims description 18
230000003197 catalytic effect Effects 0.000 title claims description 9
238000002360 preparation method Methods 0.000 title claims description 7
150000001298 alcohols Chemical class 0.000 title claims description 6
239000003054 catalyst Substances 0.000 claims description 31
238000000034 method Methods 0.000 claims description 13
229910052783 alkali metal Inorganic materials 0.000 claims description 12
150000001340 alkali metals Chemical class 0.000 claims description 12
229910052751 metal Inorganic materials 0.000 claims description 10
239000002184 metal Substances 0.000 claims description 10
239000011701 zinc Substances 0.000 claims description 10
230000015572 biosynthetic process Effects 0.000 claims description 7
150000002739 metals Chemical class 0.000 claims description 7
238000003786 synthesis reaction Methods 0.000 claims description 7
238000006243 chemical reaction Methods 0.000 claims description 6
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 4
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
229910052804 chromium Inorganic materials 0.000 claims description 4
239000011651 chromium Substances 0.000 claims description 4
229910052802 copper Inorganic materials 0.000 claims description 4
239000010949 copper Substances 0.000 claims description 4
229910052700 potassium Inorganic materials 0.000 claims description 4
239000011591 potassium Substances 0.000 claims description 4
229910052725 zinc Inorganic materials 0.000 claims description 4
229910052684 Cerium Inorganic materials 0.000 claims description 2
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
229910052782 aluminium Inorganic materials 0.000 claims description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 claims description 2
150000001875 compounds Chemical class 0.000 claims description 2
229910052746 lanthanum Inorganic materials 0.000 claims description 2
FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims description 2
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
229910052750 molybdenum Inorganic materials 0.000 claims description 2
239000011733 molybdenum Substances 0.000 claims description 2
229910052719 titanium Inorganic materials 0.000 claims description 2
239000010936 titanium Substances 0.000 claims description 2
229910052720 vanadium Inorganic materials 0.000 claims description 2
GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 12
239000000243 solution Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000007789 gas Substances 0.000 description 7
WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 6
239000011787 zinc oxide Substances 0.000 description 6
239000008367 deionised water Substances 0.000 description 5
229910021641 deionized water Inorganic materials 0.000 description 5
238000005470 impregnation Methods 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
230000000052 comparative effect Effects 0.000 description 4
239000008188 pellet Substances 0.000 description 4
SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
238000003756 stirring Methods 0.000 description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 3
OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
235000011114 ammonium hydroxide Nutrition 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
PHFQLYPOURZARY-UHFFFAOYSA-N chromium trinitrate Chemical compound [Cr+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PHFQLYPOURZARY-UHFFFAOYSA-N 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
235000011056 potassium acetate Nutrition 0.000 description 2
235000015320 potassium carbonate Nutrition 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910000272 alkali metal oxide Inorganic materials 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
JOSWYUNQBRPBDN-UHFFFAOYSA-P ammonium dichromate Chemical compound [NH4+].[NH4+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O JOSWYUNQBRPBDN-UHFFFAOYSA-P 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
238000001354 calcination Methods 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
239000003245 coal Substances 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
150000001879 copper Chemical class 0.000 description 1
229910052878 cordierite Inorganic materials 0.000 description 1
229910052593 corundum Inorganic materials 0.000 description 1
239000010431 corundum Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229940071125 manganese acetate Drugs 0.000 description 1
UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
-1 mellitus Chemical compound 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003345 natural gas Substances 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
238000005453 pelletization Methods 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/02—Monohydroxylic acyclic alcohols
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/885—Molybdenum and copper
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/86—Chromium
- B01J23/868—Chromium copper and chromium
- 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
- C07C29/15—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively
- C07C29/151—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases
- C07C29/153—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used
- 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
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

SE8206257A 1981-12-02 1982-11-03 Katalytiskt system och framstellning av blandningar av metanol och hogre alkoholer med anvendning av systemet SE451545B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT25390/81A IT1169281B (it)	1981-12-02	1981-12-02	Sistema catalitico e procedimento per la produzione di miscele di metanolo ed alcoli superiori

Publications (3)

Publication Number	Publication Date
SE8206257D0 SE8206257D0 (sv)	1982-11-03
SE8206257L SE8206257L (sv)	1983-06-03
SE451545B true SE451545B (sv)	1987-10-19

Family

ID=11216562

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8206257A SE451545B (sv)	1981-12-02	1982-11-03	Katalytiskt system och framstellning av blandningar av metanol och hogre alkoholer med anvendning av systemet

Country Status (32)

Country	Link
US (2)	US4513100A (it)
JP (1)	JPS58104635A (it)
KR (2)	KR860002159B1 (it)
AU (1)	AU550713B2 (it)
BE (1)	BE895208A (it)
BR (1)	BR8206776A (it)
CA (1)	CA1194013A (it)
CH (1)	CH650946A5 (it)
CS (1)	CS236697B2 (it)
CU (1)	CU21442A3 (it)
DD (1)	DD205680A5 (it)
DE (1)	DE3244313C2 (it)
DK (1)	DK531782A (it)
EG (1)	EG16016A (it)
ES (1)	ES8401436A1 (it)
FI (1)	FI71883C (it)
FR (1)	FR2517296A1 (it)
GB (1)	GB2110558B (it)
GR (1)	GR77106B (it)
IE (1)	IE53599B1 (it)
IN (1)	IN157897B (it)
IT (1)	IT1169281B (it)
LU (1)	LU84494A1 (it)
NO (1)	NO158722C (it)
NZ (1)	NZ202305A (it)
PH (1)	PH17792A (it)
PL (2)	PL137518B1 (it)
RO (1)	RO86064B (it)
SE (1)	SE451545B (it)
SU (1)	SU1279516A3 (it)
YU (1)	YU259682A (it)
ZA (1)	ZA827980B (it)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU565013B2 (en) *	1982-11-29	1987-09-03	Research Association For Petroleum Alternatives Development	Production of mixed alcohols
US4843101A (en) *	1983-06-01	1989-06-27	Lehigh University	Catalyst and method for producing methanol
DE3403491A1 (de) *	1984-02-02	1985-08-14	Süd-Chemie AG, 8000 München	Katalysator zur synthese von methanol und hoehere alkohole enthaltenden alkoholgemischen
US4831060A (en) *	1984-07-30	1989-05-16	The Dow Chemical Company	Mixed alcohols production from syngas
US4752622A (en) *	1984-07-30	1988-06-21	The Dow Chemical Company	Process for producing alcohols from synthesis gas
US4882360A (en) *	1984-07-30	1989-11-21	The Dow Chemical Company	Process for producing alcohols from synthesis gas
US4762858A (en) *	1985-09-16	1988-08-09	The Dow Chemical Company	Syngas conversion to oxygenates by reduced yttrium/lanthanide/actinide-modified catalyst
US4943551A (en) *	1985-11-08	1990-07-24	Union Carbide Chemicals And Plastics Company, Inc.	Catalyst for synthesis of mixtures of methanol and higher alcohols
US4681868A (en) *	1986-05-29	1987-07-21	The Standard Oil Company	Oxygenate condensation catalyst
US4789502A (en) *	1986-11-24	1988-12-06	Shell Oil Company	Carboxylic acid production
US4886651A (en) *	1988-05-18	1989-12-12	Air Products And Chemicals, Inc.	Process for co-production of higher alcohols, methanol and ammonia
US5155086A (en) *	1989-09-12	1992-10-13	Engelhard Corporation	Hydrogenation catalyst, process for preparing and process of using said catalyst
US5345005A (en) *	1989-09-12	1994-09-06	Engelhard Corporation	Hydrogenation catalyst, process for preparing and process of using said catalyst
US5070058A (en) *	1990-01-22	1991-12-03	Texaco, Inc.	Method for making a catalyst composition used in the production of lower aliphatic alcohols
US5134108A (en) *	1991-05-22	1992-07-28	Engelhard Corporation	Process for preparing catalyst with copper or zinc and with chromium, molybdenum, tungsten, or vanadium, and product thereof
US5410015A (en) *	1991-06-22	1995-04-25	Basf Aktiengesellschaft	Polyamides having a low water absorptivity
US5300695A (en) *	1992-12-07	1994-04-05	Amoco Corporation	Process for preparing alcohols
IT1276931B1 (it) *	1995-10-13	1997-11-03	Snam Progetti	Procedimento per produrre miscele di metanolo ed alcoli superiori
RU2161536C2 (ru) *	1997-03-26	2001-01-10	Институт катализа им. Г.К. Борескова СО РАН	Способ получения катализатора для низкотемпературного синтеза метанола
KR20030085284A (ko) *	2002-04-30	2003-11-05	고양복합영농조합법인	열무를 절단 포장하는 제조방법 및 그 포장 열무
US8394863B2 (en)	2003-08-21	2013-03-12	Pearson Technologies, Inc.	Process and apparatus for the production of useful products from carbonaceous feedstock
TW200519072A (en) *	2003-08-21	2005-06-16	Pearson Technologies Inc	Process and apparatus for the production of useful products from carbonaceous feedstock
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1981
- 1981-12-02 IT IT25390/81A patent/IT1169281B/it active
1982
- 1982-10-28 US US06/437,439 patent/US4513100A/en not_active Expired - Lifetime
- 1982-10-28 NZ NZ202305A patent/NZ202305A/en unknown
- 1982-10-29 NO NO823601A patent/NO158722C/no unknown
- 1982-11-01 CA CA000414582A patent/CA1194013A/en not_active Expired
- 1982-11-01 ZA ZA827980A patent/ZA827980B/xx unknown
- 1982-11-03 SE SE8206257A patent/SE451545B/sv not_active IP Right Cessation
- 1982-11-04 AU AU90168/82A patent/AU550713B2/en not_active Ceased
- 1982-11-05 PH PH28093A patent/PH17792A/en unknown
- 1982-11-05 GB GB08231640A patent/GB2110558B/en not_active Expired
- 1982-11-09 KR KR8205053A patent/KR860002159B1/ko not_active Expired
- 1982-11-09 GR GR69769A patent/GR77106B/el unknown
- 1982-11-19 ES ES517749A patent/ES8401436A1/es not_active Expired
- 1982-11-22 YU YU02596/82A patent/YU259682A/xx unknown
- 1982-11-22 BR BR8206776A patent/BR8206776A/pt unknown
- 1982-11-25 CS CS828464A patent/CS236697B2/cs unknown
- 1982-11-26 SU SU3516802A patent/SU1279516A3/ru active
- 1982-11-26 FR FR8219935A patent/FR2517296A1/fr active Granted
- 1982-11-29 LU LU84494A patent/LU84494A1/xx unknown
- 1982-11-29 DD DD82245316A patent/DD205680A5/de unknown
- 1982-11-30 RO RO109181A patent/RO86064B/ro unknown
- 1982-11-30 DK DK531782A patent/DK531782A/da not_active Application Discontinuation
- 1982-11-30 CH CH6960/82A patent/CH650946A5/it not_active IP Right Cessation
- 1982-11-30 DE DE3244313A patent/DE3244313C2/de not_active Expired
- 1982-12-01 EG EG708/82A patent/EG16016A/xx active
- 1982-12-01 CU CU8125390AA patent/CU21442A3/es unknown
- 1982-12-01 BE BE0/209617A patent/BE895208A/fr not_active IP Right Cessation
- 1982-12-01 PL PL1982239300A patent/PL137518B1/pl unknown
- 1982-12-01 PL PL1982248949A patent/PL138697B1/pl unknown
- 1982-12-01 IE IE2861/82A patent/IE53599B1/en unknown
- 1982-12-02 JP JP57210701A patent/JPS58104635A/ja active Granted
- 1982-12-02 FI FI824150A patent/FI71883C/fi not_active IP Right Cessation
- 1982-12-02 IN IN1403/CAL/82A patent/IN157897B/en unknown
1986
- 1986-10-16 US US06/918,668 patent/US4778827A/en not_active Expired - Fee Related
- 1986-10-24 KR KR1019860008931A patent/KR890004344B1/ko not_active Expired

Also Published As

Publication number	Publication date
CA1194013A (en)	1985-09-24
DE3244313C2 (de)	1986-02-06
JPH0336571B2 (it)	1991-05-31
GR77106B (it)	1984-09-06
FI71883C (fi)	1987-03-09
YU259682A (en)	1985-06-30
LU84494A1 (fr)	1983-09-08
SE8206257D0 (sv)	1982-11-03
CH650946A5 (it)	1985-08-30
PL138697B1 (en)	1986-10-31
NZ202305A (en)	1985-07-31
RO86064B (ro)	1985-04-02
NO823601L (no)	1983-06-03
AU550713B2 (en)	1986-04-10
IN157897B (it)	1986-07-19
IE53599B1 (en)	1988-12-21
DK531782A (da)	1983-06-03
CU21442A3 (en)	1987-01-13
KR840002259A (ko)	1984-06-25
NO158722B (no)	1988-07-18
IT1169281B (it)	1987-05-27
ZA827980B (en)	1983-12-28
GB2110558A (en)	1983-06-22
ES517749A0 (es)	1983-12-16
PL137518B1 (en)	1986-06-30
JPS58104635A (ja)	1983-06-22
NO158722C (no)	1988-10-26
SU1279516A3 (ru)	1986-12-23
DE3244313A1 (de)	1983-06-16
FI824150L (fi)	1983-06-03
US4778827A (en)	1988-10-18
BE895208A (fr)	1983-06-01
AU9016882A (en)	1983-06-09
FI824150A0 (fi)	1982-12-02
DD205680A5 (de)	1984-01-04
IE822861L (en)	1983-06-02
EG16016A (en)	1988-01-31
FR2517296A1 (fr)	1983-06-03
ES8401436A1 (es)	1983-12-16
FI71883B (fi)	1986-11-28
PL239300A1 (en)	1983-07-18
KR880005848A (ko)	1988-06-30
GB2110558B (en)	1985-01-23
RO86064A (ro)	1985-03-15
US4513100A (en)	1985-04-23
PH17792A (en)	1984-12-13
FR2517296B1 (it)	1985-04-19
CS236697B2 (en)	1985-05-15
IT8125390A0 (it)	1981-12-02
KR890004344B1 (ko)	1989-10-31
BR8206776A (pt)	1983-10-04
KR860002159B1 (ko)	1986-12-22
SE8206257L (sv)	1983-06-03

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SA99626044B1 (ar)	2006-10-31	الأكسدة الحفزية catalytic oxidation للألكانات alkanes الى الأحماض acids المقابلة
BR0104821B1 (pt)	2012-10-02	processo de oxidação para a produção de alcenos e ácidos carboxìlicos.
EP0460932A2 (en)	1991-12-11	Method for preparing acrolein or methacrolein
EP1986986A2 (en)	2008-11-05	Process of making mixed metal oxide catalysts for the production of unsaturated aldehydes from olefins
SA98190657B1 (ar)	2006-05-23	حفاز عملية الأموكسدة ammoxidation للإستخدام في إنتاج أكريلو نيتريل acrylonitrile أو ميثأكريلو نيتريل methacrylonitrile من بروبان propane أو أيزوبيوتان isobutane بواسطة عملية الأموكسدة ammoxidation
US7217679B2 (en)	2007-05-15	Catalytic coating for the hydrogenation of maleic anhydride and related compounds to give γ-butyrolactone, tetrahydrofuran and derivatives thereof
JP3497558B2 (ja)	2004-02-16	アンモ酸化用触媒組成物及びこれを用いたアクリロニトリルまたはメタクリロニトリルの製造方法
RU2233832C2 (ru)	2004-08-10	Способ получения уксусной кислоты
JPH05154383A (ja)	1993-06-22	一酸化炭素又は二酸化炭素の水素化反応用触媒
WO2022015680A1 (en)	2022-01-20	Process and catalyst for oxidative esterication with mechanically strong and chemically resistant catalyst
US4446328A (en)	1984-05-01	Process for producing methacrolein
JP2813770B2 (ja)	1998-10-22	エタノールの製造方法
JP7029346B2 (ja)	2022-03-03	インデンの製造方法
US4347383A (en)	1982-08-31	Process for producing benzophenone-azines
JPS6041544A (ja)	1985-03-05	アルキルアミン類の製造のための触媒および方法
US20050032627A1 (en)	2005-02-10	Method for producing toluol derivatives
JP2005515248A6 (ja)	2005-08-04	トルオール誘導体の製造方法
JPH0133097B2 (it)	1989-07-11
JPH0133217B2 (it)	1989-07-12
EP0452695B1 (en)	1994-08-03	Production of a catalyst and its use for producing phenol

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