DE2648443C2 - Verfahren zur Herstellung von olefinisch ungesättigter Verbindungen durch nicht-oxidative Dehydrierung in Gegenwart eines Spinell-Katalysators - Google Patents
Verfahren zur Herstellung von olefinisch ungesättigter Verbindungen durch nicht-oxidative Dehydrierung in Gegenwart eines Spinell-KatalysatorsInfo
- Publication number
- DE2648443C2 DE2648443C2 DE2648443A DE2648443A DE2648443C2 DE 2648443 C2 DE2648443 C2 DE 2648443C2 DE 2648443 A DE2648443 A DE 2648443A DE 2648443 A DE2648443 A DE 2648443A DE 2648443 C2 DE2648443 C2 DE 2648443C2
- Authority
- DE
- Germany
- Prior art keywords
- unsaturated compounds
- spinel
- oxidative dehydrogenation
- catalysts
- olefinically unsaturated
- 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.)
- Expired
Links
- 239000003054 catalyst Substances 0.000 title claims description 20
- 150000001875 compounds Chemical class 0.000 title claims description 14
- 238000000034 method Methods 0.000 title claims description 11
- 229910052596 spinel Inorganic materials 0.000 title claims description 11
- 239000011029 spinel Substances 0.000 title claims description 11
- 238000002360 preparation method Methods 0.000 title claims description 5
- 238000005839 oxidative dehydrogenation reaction Methods 0.000 title claims 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 238000006356 dehydrogenation reaction Methods 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 5
- 229910052700 potassium Inorganic materials 0.000 claims description 5
- 239000011591 potassium Substances 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims 2
- 229910017052 cobalt Inorganic materials 0.000 claims 2
- 239000010941 cobalt Substances 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229910000859 α-Fe Inorganic materials 0.000 claims 2
- SYWDWCWQXBUCOP-UHFFFAOYSA-N benzene;ethene Chemical compound C=C.C1=CC=CC=C1 SYWDWCWQXBUCOP-UHFFFAOYSA-N 0.000 claims 1
- 150000001868 cobalt Chemical class 0.000 claims 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 1
- -1 ethylene benzene Chemical class 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 16
- 239000011651 chromium Substances 0.000 description 4
- 229910052792 caesium Inorganic materials 0.000 description 3
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 1
- 229910021555 Chromium Chloride Inorganic materials 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- QSWDMMVNRMROPK-UHFFFAOYSA-K chromium(3+) trichloride Chemical compound [Cl-].[Cl-].[Cl-].[Cr+3] QSWDMMVNRMROPK-UHFFFAOYSA-K 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011874 heated mixture Substances 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
Classifications
-
- 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
- B01J23/862—Iron and chromium
-
- 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
-
- 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
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3335—Catalytic processes with metals
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7532908A FR2329620A1 (fr) | 1975-10-28 | 1975-10-28 | Procede de deshydrogenation non-oxydante |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2648443A1 DE2648443A1 (de) | 1977-05-05 |
| DE2648443C2 true DE2648443C2 (de) | 1986-02-06 |
Family
ID=9161732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2648443A Expired DE2648443C2 (de) | 1975-10-28 | 1976-10-26 | Verfahren zur Herstellung von olefinisch ungesättigter Verbindungen durch nicht-oxidative Dehydrierung in Gegenwart eines Spinell-Katalysators |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS603289B2 (enExample) |
| CA (1) | CA1072987A (enExample) |
| DE (1) | DE2648443C2 (enExample) |
| FR (1) | FR2329620A1 (enExample) |
| GB (1) | GB1550873A (enExample) |
| IT (1) | IT1069010B (enExample) |
| NL (1) | NL7611828A (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2411169A1 (fr) * | 1977-12-12 | 1979-07-06 | Shell France | Procede de deshydrogenation sans oxydation et composition catalytique pour la mise en oeuvre de ce procede |
| FR2497192A1 (fr) * | 1980-12-29 | 1982-07-02 | Shell France | Procede de deshydrogenation non oxydante |
| FR2511671A1 (fr) * | 1981-08-18 | 1983-02-25 | Davy Mckee Ag | Procede de deshydrogenation |
| DE19715203A1 (de) * | 1997-04-11 | 1998-10-15 | Basf Ag | Katalysator und Verfahren zur Seitenkettenalkylierung |
| EP4603470A1 (en) * | 2024-02-19 | 2025-08-20 | Dow Global Technologies LLC | Methods for converting alkanes to alkenes using steam tolerant dehydrogenation catalysts with spinel structures |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3291756A (en) * | 1964-01-09 | 1966-12-13 | Baugh Chemical Company | Catalytic dehydrogenation |
| US3364277A (en) * | 1965-05-21 | 1968-01-16 | Shell Oil Co | Dehydrogenating olefins to diolefins in the presence of a yellow iron oxide catalyst |
| US3360579A (en) * | 1965-05-21 | 1967-12-26 | Shell Oil Co | Catalytic dehydrogenation of alkylaromatics |
| US3420912A (en) * | 1967-01-27 | 1969-01-07 | Petro Tex Chem Corp | Dehydrogenation process using manganese ferrite |
| BE790702A (fr) * | 1970-07-10 | 1973-04-27 | Dow Chemical Co | Procede de fabrication d'un catalyseur de deshydrogenation, catalyseur obtenu et son application a la fabrication d'hydrocarburesvinylaromatiques |
| US3781376A (en) * | 1971-06-30 | 1973-12-25 | Petro Tex Chem Corp | Dehydrogenation process and catalyst |
-
1975
- 1975-10-28 FR FR7532908A patent/FR2329620A1/fr active Granted
-
1976
- 1976-10-07 CA CA262,968A patent/CA1072987A/en not_active Expired
- 1976-10-26 GB GB44428/76A patent/GB1550873A/en not_active Expired
- 1976-10-26 NL NL7611828A patent/NL7611828A/xx not_active Application Discontinuation
- 1976-10-26 IT IT28713/76A patent/IT1069010B/it active
- 1976-10-26 DE DE2648443A patent/DE2648443C2/de not_active Expired
- 1976-10-26 JP JP51127901A patent/JPS603289B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CA1072987A (en) | 1980-03-04 |
| DE2648443A1 (de) | 1977-05-05 |
| JPS603289B2 (ja) | 1985-01-26 |
| GB1550873A (en) | 1979-08-22 |
| JPS5253803A (en) | 1977-04-30 |
| FR2329620A1 (fr) | 1977-05-27 |
| FR2329620B1 (enExample) | 1979-01-19 |
| IT1069010B (it) | 1985-03-21 |
| NL7611828A (nl) | 1977-05-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8128 | New person/name/address of the agent |
Representative=s name: JUNG, E., DIPL.-CHEM. DR.PHIL. SCHIRDEWAHN, J., DI |
|
| 8110 | Request for examination paragraph 44 | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |