DE1231675B - Verfahren zur Herstellung von Katalysatoren fuer die Herstellung von Acrolein, Acrylnitril und deren Alkylderivaten - Google Patents
Verfahren zur Herstellung von Katalysatoren fuer die Herstellung von Acrolein, Acrylnitril und deren AlkylderivatenInfo
- Publication number
- DE1231675B DE1231675B DES78512A DES0078512A DE1231675B DE 1231675 B DE1231675 B DE 1231675B DE S78512 A DES78512 A DE S78512A DE S0078512 A DES0078512 A DE S0078512A DE 1231675 B DE1231675 B DE 1231675B
- Authority
- DE
- Germany
- Prior art keywords
- production
- antimony
- tin
- catalysts
- acrylonitrile
- 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
- 239000003054 catalyst Substances 0.000 title claims description 27
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 title claims description 12
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 title claims description 8
- 125000000217 alkyl group Chemical group 0.000 title claims description 5
- 238000000034 method Methods 0.000 title claims description 4
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 11
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 9
- 229910052787 antimony Inorganic materials 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 7
- 229910017604 nitric acid Inorganic materials 0.000 claims description 7
- 229910000410 antimony oxide Inorganic materials 0.000 claims description 6
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical class [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims description 6
- 229910001887 tin oxide Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 239000011872 intimate mixture Substances 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 4
- 229910001245 Sb alloy Inorganic materials 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000002244 precipitate Substances 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 3
- 229910001128 Sn alloy Inorganic materials 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 4
- 229910006913 SnSb Inorganic materials 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- WMHSAFDEIXKKMV-UHFFFAOYSA-N oxoantimony;oxotin Chemical compound [Sn]=O.[Sb]=O WMHSAFDEIXKKMV-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000007669 thermal treatment Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000004438 BET method Methods 0.000 description 1
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002140 antimony alloy Substances 0.000 description 1
- GVFOJDIFWSDNOY-UHFFFAOYSA-N antimony tin Chemical compound [Sn].[Sb] GVFOJDIFWSDNOY-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/24—Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons
- C07C253/26—Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons containing carbon-to-carbon multiple bonds, e.g. unsaturated aldehydes
-
- 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
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/18—Arsenic, antimony or bismuth
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
- C07C45/35—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/615—100-500 m2/g
-
- 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)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1231675X | 1961-03-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1231675B true DE1231675B (de) | 1967-01-05 |
Family
ID=9677582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DES78512A Pending DE1231675B (de) | 1961-03-29 | 1962-03-15 | Verfahren zur Herstellung von Katalysatoren fuer die Herstellung von Acrolein, Acrylnitril und deren Alkylderivaten |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE1231675B (US08063081-20111122-C00044.png) |
| NL (1) | NL276444A (US08063081-20111122-C00044.png) |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE587683A (US08063081-20111122-C00044.png) * | 1959-02-17 | |||
| BE587685A (US08063081-20111122-C00044.png) * | 1959-04-02 | |||
| AT180257B (de) * | 1951-11-08 | 1954-11-25 | Distillers Co Yeast Ltd | Verfahren zur Herstellung von praktisch reinen, ungesättigten Nitrilen |
| US2904580A (en) * | 1959-02-24 | 1959-09-15 | Standard Oil Co | Process for the manufacture of acrylonitrile |
| FR1219512A (fr) * | 1958-04-16 | 1960-05-18 | Distillers Co Yeast Ltd | Procédé pour la préparation de nitriles aliphatiques à partir d'oléfines |
| BE587684A (fr) * | 1959-02-17 | 1960-08-16 | Distillers Co Yeast Ltd | Production d'aldéhydes aliphatiques non saturés |
| FR1247785A (fr) * | 1959-02-12 | 1960-12-02 | Distillers Co Yeast Ltd | Procédé de production d'acrylonitrile et de méthacrylonitrile |
| FR1255121A (fr) * | 1959-02-16 | 1961-03-03 | Asahi Chemical Ind | Procédé de production de nitriles non saturés |
| FR1261568A (fr) * | 1962-12-08 | 1961-05-19 | Distillers Co Yeast Ltd | Procédé de production d'acrylonitrile ou de méthacrylonitrile |
| FR1272308A (fr) * | 1959-10-28 | 1961-09-22 | Distillers Co Yeast Ltd | Procédé de production de nitriles aliphatiques non saturés |
-
0
- NL NL276444D patent/NL276444A/xx unknown
-
1962
- 1962-03-15 DE DES78512A patent/DE1231675B/de active Pending
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT180257B (de) * | 1951-11-08 | 1954-11-25 | Distillers Co Yeast Ltd | Verfahren zur Herstellung von praktisch reinen, ungesättigten Nitrilen |
| FR1219512A (fr) * | 1958-04-16 | 1960-05-18 | Distillers Co Yeast Ltd | Procédé pour la préparation de nitriles aliphatiques à partir d'oléfines |
| FR1247785A (fr) * | 1959-02-12 | 1960-12-02 | Distillers Co Yeast Ltd | Procédé de production d'acrylonitrile et de méthacrylonitrile |
| FR1255121A (fr) * | 1959-02-16 | 1961-03-03 | Asahi Chemical Ind | Procédé de production de nitriles non saturés |
| BE587683A (US08063081-20111122-C00044.png) * | 1959-02-17 | |||
| BE587684A (fr) * | 1959-02-17 | 1960-08-16 | Distillers Co Yeast Ltd | Production d'aldéhydes aliphatiques non saturés |
| US2904580A (en) * | 1959-02-24 | 1959-09-15 | Standard Oil Co | Process for the manufacture of acrylonitrile |
| BE587685A (US08063081-20111122-C00044.png) * | 1959-04-02 | |||
| FR1272308A (fr) * | 1959-10-28 | 1961-09-22 | Distillers Co Yeast Ltd | Procédé de production de nitriles aliphatiques non saturés |
| FR1261568A (fr) * | 1962-12-08 | 1961-05-19 | Distillers Co Yeast Ltd | Procédé de production d'acrylonitrile ou de méthacrylonitrile |
Also Published As
| Publication number | Publication date |
|---|---|
| NL276444A (US08063081-20111122-C00044.png) |
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