GB798564A - Improvements in or relating to the preparation of olefinic carbonylic compounds - Google Patents
Improvements in or relating to the preparation of olefinic carbonylic compoundsInfo
- Publication number
- GB798564A GB798564A GB17193/56A GB1719356A GB798564A GB 798564 A GB798564 A GB 798564A GB 17193/56 A GB17193/56 A GB 17193/56A GB 1719356 A GB1719356 A GB 1719356A GB 798564 A GB798564 A GB 798564A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrazine
- support
- copper
- mixture
- reducing agent
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 10
- 239000003638 chemical reducing agent Substances 0.000 abstract 9
- 150000001879 copper Chemical class 0.000 abstract 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 7
- 229910052802 copper Inorganic materials 0.000 abstract 7
- 239000010949 copper Substances 0.000 abstract 7
- 229930195733 hydrocarbon Natural products 0.000 abstract 7
- 150000002430 hydrocarbons Chemical class 0.000 abstract 7
- 239000000203 mixture Substances 0.000 abstract 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 6
- 238000010438 heat treatment Methods 0.000 abstract 6
- 239000001301 oxygen Substances 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 5
- 239000004215 Carbon black (E152) Substances 0.000 abstract 5
- 239000000908 ammonium hydroxide Substances 0.000 abstract 5
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 4
- 239000011261 inert gas Substances 0.000 abstract 4
- 230000003647 oxidation Effects 0.000 abstract 4
- 238000007254 oxidation reaction Methods 0.000 abstract 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 4
- 239000012266 salt solution Substances 0.000 abstract 4
- 229910010271 silicon carbide Inorganic materials 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 3
- 150000002429 hydrazines Chemical class 0.000 abstract 3
- 239000000463 material Substances 0.000 abstract 3
- 239000007787 solid Substances 0.000 abstract 3
- 239000000243 solution Substances 0.000 abstract 3
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract 2
- 229910052580 B4C Inorganic materials 0.000 abstract 2
- 229910052582 BN Inorganic materials 0.000 abstract 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- 239000005909 Kieselgur Substances 0.000 abstract 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 abstract 2
- 229910002651 NO3 Inorganic materials 0.000 abstract 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- 229910026551 ZrC Inorganic materials 0.000 abstract 2
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 abstract 2
- -1 alpha Chemical class 0.000 abstract 2
- 229910001570 bauxite Inorganic materials 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 229910052804 chromium Inorganic materials 0.000 abstract 2
- 239000011651 chromium Substances 0.000 abstract 2
- 239000011248 coating agent Substances 0.000 abstract 2
- 238000000576 coating method Methods 0.000 abstract 2
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 abstract 2
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 abstract 2
- 229940112669 cuprous oxide Drugs 0.000 abstract 2
- 230000008021 deposition Effects 0.000 abstract 2
- 229910052731 fluorine Inorganic materials 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- 239000000499 gel Substances 0.000 abstract 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052737 gold Inorganic materials 0.000 abstract 2
- 239000010931 gold Substances 0.000 abstract 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 abstract 2
- ZGCHATBSUIJLRL-UHFFFAOYSA-N hydrazine sulfate Chemical compound NN.OS(O)(=O)=O ZGCHATBSUIJLRL-UHFFFAOYSA-N 0.000 abstract 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 2
- 229910000040 hydrogen fluoride Inorganic materials 0.000 abstract 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 2
- 239000000395 magnesium oxide Substances 0.000 abstract 2
- 239000011733 molybdenum Substances 0.000 abstract 2
- 229910000476 molybdenum oxide Inorganic materials 0.000 abstract 2
- 229910017604 nitric acid Inorganic materials 0.000 abstract 2
- 230000001590 oxidative effect Effects 0.000 abstract 2
- VVRQVWSVLMGPRN-UHFFFAOYSA-N oxotungsten Chemical class [W]=O VVRQVWSVLMGPRN-UHFFFAOYSA-N 0.000 abstract 2
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 abstract 2
- 229940067157 phenylhydrazine Drugs 0.000 abstract 2
- 229910052697 platinum Inorganic materials 0.000 abstract 2
- 239000008262 pumice Substances 0.000 abstract 2
- 239000000741 silica gel Substances 0.000 abstract 2
- 229910002027 silica gel Inorganic materials 0.000 abstract 2
- 239000010703 silicon Substances 0.000 abstract 2
- 229910052710 silicon Inorganic materials 0.000 abstract 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052709 silver Inorganic materials 0.000 abstract 2
- 239000004332 silver Substances 0.000 abstract 2
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 2
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 abstract 2
- 229910001930 tungsten oxide Inorganic materials 0.000 abstract 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 1
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 abstract 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052726 zirconium Inorganic materials 0.000 abstract 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
- B01J23/72—Copper
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Olefinic carbonylic compounds, e.g. alpha, beta-unsaturated aldehydes and ketones, are prepared by the incomplete oxidation of an olefinic hydrocarbon with oxygen or a gas containing oxygen in the presence of a supported copper-containing catalyst which has been prepared by contacting a solid support material at 10-150 DEG C. with a mixture of a solution of a copper salt, ammonium hydroxide, and a reducing agent comprising hydrazine or a hydrazine derivative (see Group III). Acrolein and methacrolein may be formed from propylene and isobutylene respectively. Examples describe the oxidation of propylene (a) at 250-300 DEG C., atmospheric pressure, and a propylene to oxygen mol. ratio of 10 : 1; (b) at 400 DEG C., 85 lbs. per sq. in. pressure, and a propylene to oxygen mol. ratio of 8 : 1. Water vapour may be added to the charge.ALSO:A supported copper-containing catalyst, for the oxidation of olefinic hydrocarbons to olefinic carbonylic compounds (see Group IV (b)), is prepared by contacting a solid support material at 10-150 DEG C. with a mixture of a solution of a copper salt, ammonium hydroxide, and a reducing agent comprising hydrazine or a hydrazine derivative. The reducing agent may be added to a mixture of the copper salt solution, ammonium hydroxide, and the support; alternatively the support may be preheated, e.g. to 40-100 DEG C., and contacted with a mixture of the reducing agent and the ammoniacal copper salt solution. After formation of the deposit of copper, the support may be washed and dried in air or an atmosphere of a hydrocarbon or an inert gas at 100-250 DEG C. Suitable copper salts are the acetate, chloride, nitrate, and sulphate. The preferred reducing agents are hydrazine and hydrazine hydrate, but phenyl hydrazine and hydrazine sulphate may also be used. The support is preferably granular and may be composed of pumice, diatomaceous earth silica gel, silicon, silicon carbide, boron carbide, carborundum, alumina, carbon, magnesia, thoria, bauxite, sandstone, crushed firebrick, majolica, fused zirconia, silica-alumina, gels of chromium, molybdenum, or tungsten oxides, zirconium carbide, circonium boride, or boron nitride. The support may be pretreated by heating in steam or inert gas, treatment with hydrogen chloride, nitric acid, or hydrogen fluoride, contact with iodine, chlorine, or fluorine, or by deposition of minor amounts of silver, gold, or platinum. The copper coating on the support may be converted to cuprous oxide by heating to 100-250 DEG C. in an oxidizing atmosphere or by heating to 100-600 DEG C. in an atmosphere of a hydrocarbon and oxygen.ALSO:A supported copper-containing catalyst, for the oxidation of olefinic hydrocarbons to olefinic carbonylic compounds (see Group IV(b)), is prepared by contacting a solid support material at 10 DEG -150 DEG C. with a mixture of a solution of a copper salt, ammonium hydroxide, and a reducing agent comprising hydrazine or a hydrazine derivative. The reducing agent may be added to a mixture of the copper salt solution, ammonium hydroxide, and the support; alternatively the support may be preheated, e.g. to 40 DEG -100 DEG C., and contacted with a mixture of the reducing agent and the ammoniacal copper salt solution. After formation of the deposit of copper, the support may be washed and dried in air or an atmosphere of a hydrocarbon or an inert gas at 100 DEG -250 DEG C. Suitable copper salts are the acetate, chloride, nitrate, and sulphate. The preferred reducing agents are hydrazine and hydrazine hydrate, but phenyl hydrazine and hydrazine sulphate may also be used. The support is preferably granular and may be composed of pumice, diatomaceous earth, silica gel, silicon, silicon carbide, boron carbide, carborundum, alumina, carbon, magnesia, thoria, bauxite, sandstone, crushed firebrick, majolica, fused zirconia, silica-alumina, gels of chromium, molybdenum, or tungsten oxides, zirconium carbide, zirconium boride, or boron nitride. The support may be pretreated by heating in steam or inert gas, treatment with hydrogen chloride, nitric acid, or hydrogen fluoride, contact with iodine, chlorine, or fluorine, or by deposition of minor amounts of silver, gold, or platinum. The copper coating on the support may be converted to cuprous oxide by heating to 100 DEG -250 DEG C. in an oxidizing atmosphere or by heating to 100 DEG -600 DEG C. in an atmosphere of a hydrocarbon and oxygen.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US798564XA | 1955-06-06 | 1955-06-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB798564A true GB798564A (en) | 1958-07-23 |
Family
ID=22153232
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB17193/56A Expired GB798564A (en) | 1955-06-06 | 1956-06-04 | Improvements in or relating to the preparation of olefinic carbonylic compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB798564A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114479990A (en) * | 2022-02-09 | 2022-05-13 | 王旭锋 | Lubricating oil additive and preparation method and application thereof |
-
1956
- 1956-06-04 GB GB17193/56A patent/GB798564A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114479990A (en) * | 2022-02-09 | 2022-05-13 | 王旭锋 | Lubricating oil additive and preparation method and application thereof |
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