DE1568043A1 - Verfahren zur katalytischen Hydrierung von aromatischen Kohlenwasserstoffen - Google Patents
Verfahren zur katalytischen Hydrierung von aromatischen KohlenwasserstoffenInfo
- Publication number
- DE1568043A1 DE1568043A1 DE19661568043 DE1568043A DE1568043A1 DE 1568043 A1 DE1568043 A1 DE 1568043A1 DE 19661568043 DE19661568043 DE 19661568043 DE 1568043 A DE1568043 A DE 1568043A DE 1568043 A1 DE1568043 A1 DE 1568043A1
- Authority
- DE
- Germany
- Prior art keywords
- reaction zone
- aromatic hydrocarbon
- hydrocarbon
- cycloaliphatic
- hydrogenation
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 15
- 150000004945 aromatic hydrocarbons Chemical class 0.000 title claims description 11
- 238000009903 catalytic hydrogenation reaction Methods 0.000 title claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 46
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 30
- 229930195733 hydrocarbon Natural products 0.000 claims description 15
- 150000002430 hydrocarbons Chemical class 0.000 claims description 15
- 239000003054 catalyst Substances 0.000 claims description 14
- 238000005984 hydrogenation reaction Methods 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 239000007791 liquid phase Substances 0.000 claims description 7
- 239000007792 gaseous phase Substances 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 5
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 230000003134 recirculating effect Effects 0.000 claims 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 7
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001934 cyclohexanes Chemical class 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 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
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- -1 cyolohexane Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011874 heated mixture Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
- C07C5/10—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of aromatic six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- 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
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/8995—Catalyst and recycle considerations
- Y10S585/901—Catalyst and recycle considerations with recycle, rehabilitation, or preservation of solvent, diluent, or mass action agent
-
- 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
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/8995—Catalyst and recycle considerations
- Y10S585/903—Catalyst and recycle considerations with hydrocarbon recycle to control synthesis reaction, e.g. by cooling, quenching
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US493415A US3387049A (en) | 1965-10-06 | 1965-10-06 | Catalytic hydrogenation of aromatic hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1568043A1 true DE1568043A1 (de) | 1970-04-30 |
Family
ID=23960139
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19661568043 Pending DE1568043A1 (de) | 1965-10-06 | 1966-10-05 | Verfahren zur katalytischen Hydrierung von aromatischen Kohlenwasserstoffen |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3387049A (enExample) |
| JP (1) | JPS5521017B1 (enExample) |
| DE (1) | DE1568043A1 (enExample) |
| ES (1) | ES331995A1 (enExample) |
| GB (1) | GB1152710A (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3541169A (en) * | 1968-01-09 | 1970-11-17 | Ashland Oil Inc | Naphthalene hydrogenation |
| US4036734A (en) * | 1973-11-02 | 1977-07-19 | Exxon Research And Engineering Company | Process for manufacturing naphthenic solvents and low aromatics mineral spirits |
| US3996304A (en) * | 1974-06-19 | 1976-12-07 | Universal Oil Products Company | Hydroprocessing of hydrocarbons |
| US3992464A (en) * | 1974-11-08 | 1976-11-16 | Uop Inc. | Hydroprocessing aromatics to make cycloparaffins |
| US4003954A (en) * | 1975-01-02 | 1977-01-18 | Uop Inc. | Hydroprocessing aromatics to make cycloparaffins |
| US4849093A (en) * | 1987-02-02 | 1989-07-18 | Union Oil Company Of California | Catalytic aromatic saturation of hydrocarbons |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3254134A (en) * | 1965-04-05 | 1966-05-31 | Texaco Inc | Plural stage hydrogenation of aromatics |
-
1965
- 1965-10-06 US US493415A patent/US3387049A/en not_active Expired - Lifetime
-
1966
- 1966-10-05 DE DE19661568043 patent/DE1568043A1/de active Pending
- 1966-10-06 JP JP6548166A patent/JPS5521017B1/ja active Pending
- 1966-10-06 GB GB44698/66A patent/GB1152710A/en not_active Expired
- 1966-10-10 ES ES0331995A patent/ES331995A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US3387049A (en) | 1968-06-04 |
| ES331995A1 (es) | 1967-11-16 |
| GB1152710A (en) | 1969-05-21 |
| JPS5521017B1 (enExample) | 1980-06-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2627678C2 (de) | Verfahren zur Umwandlung von Kohlenwasserstoffen unter Gewinnung von leichten Kohlenwasserstoffdestillatfraktionen | |
| DE1693025C2 (de) | Verfahren zur zweistufigen katalytischen Hydrierung von Benzol zu Cyclohexan | |
| DE68910192T2 (de) | Verfahren zur Dehydrierung von Kohlenwasserstoffen die aus einer Kombination von isothermischen und adiabatischen Stufen zusammengesetzt sind. | |
| DE1643120B2 (de) | Verfahren zur herstellung von vinylaromatischen kohlenwasserstoffen durch katalytische dehydrierung von alkylaromatischen kohlenwasserstoffen | |
| DE1568043A1 (de) | Verfahren zur katalytischen Hydrierung von aromatischen Kohlenwasserstoffen | |
| DE2431436A1 (de) | Verfahren zur herstellung von duesentreibstoff | |
| DE2127625A1 (enExample) | ||
| DE2219949B2 (de) | Verfahren zur Herstellung von methanreichen Gasprodukten durch katalytisch« Wasserdampfreformierung einer Kohlenwasserstoffbeschickung | |
| DE2426499A1 (de) | Verfahren zur herstellung von styrol oder styrolhomologen | |
| DE1668776A1 (de) | Katalytisches Umwandlungsverfahren fuer Kohlenwasserstoffe | |
| DE1643576C3 (de) | Verfahren zur vollständigen Hydrierung eines aromatischen Kohlenwasserstoffs | |
| DE1909760A1 (de) | Verfahren zur katalytischen Herstellung von Cycloparaffinen durch Hydrierung der entsprechenden aromatischep Kohlenwasserstoffe | |
| DE1917279A1 (de) | Verfahren zur katalytischen Dehydrierung eines alkylierten aromatischen Kohlenwasserstoffes | |
| DE1468780A1 (de) | Verfahren und Vorrichtung zur Herstellung von Cyclohexan | |
| DE1568362A1 (de) | Verfahren zur Herstellung von Adamantan | |
| DE2038266A1 (de) | Verfahren und Vorrichtung zur Herstellung von Propylen | |
| DE2404139A1 (de) | Verfahren zur erhoehung des methangehaltes von methanhaltigen gasen | |
| DE2219748A1 (de) | Verfahren zur Herstellung von Äthylenoxid | |
| EP0285004B1 (de) | Verfahren zur Herstellung von Dimethylether | |
| DE2148430A1 (en) | Catalytic reforming of hydrocarbons - to gas contg at least 80% hydrogen and carbon monoxide | |
| DE3047502C2 (enExample) | ||
| AT236360B (de) | Verfahren zur Dehyrierung eines alkylierten aromatischen Kohlenwasserstoffes | |
| AT277182B (de) | Verfahren zur Herstellung von 1,2-Dichloräthan | |
| DE1418894C3 (enExample) | ||
| DE1793448C (de) | Verfahren zur Herstellung von Benzol durch thermische hydrierende Entmethylierung von Toluol |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHJ | Non-payment of the annual fee |