GB331185A - Improvements in the manufacture and production of aldehydes from 1.2-oxides of hydrocarbons - Google Patents
Improvements in the manufacture and production of aldehydes from 1.2-oxides of hydrocarbonsInfo
- Publication number
- GB331185A GB331185A GB870929A GB870929A GB331185A GB 331185 A GB331185 A GB 331185A GB 870929 A GB870929 A GB 870929A GB 870929 A GB870929 A GB 870929A GB 331185 A GB331185 A GB 331185A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxides
- oxide
- catalysts
- aldehydes
- over
- 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
- 150000001299 aldehydes Chemical class 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 2
- 229930195733 hydrocarbon Natural products 0.000 title 1
- 150000002430 hydrocarbons Chemical class 0.000 title 1
- 239000003054 catalyst Substances 0.000 abstract 7
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 6
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 abstract 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 abstract 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 150000004679 hydroxides Chemical class 0.000 abstract 2
- 150000002576 ketones Chemical class 0.000 abstract 2
- 235000012054 meals Nutrition 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- MXZRMHIULZDAKC-UHFFFAOYSA-L ammonium magnesium phosphate Chemical compound [NH4+].[Mg+2].[O-]P([O-])([O-])=O MXZRMHIULZDAKC-UHFFFAOYSA-L 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 abstract 1
- 229910001863 barium hydroxide Inorganic materials 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229940116318 copper carbonate Drugs 0.000 abstract 1
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 abstract 1
- XZTWHWHGBBCSMX-UHFFFAOYSA-J dimagnesium;phosphonato phosphate Chemical compound [Mg+2].[Mg+2].[O-]P([O-])(=O)OP([O-])([O-])=O XZTWHWHGBBCSMX-UHFFFAOYSA-J 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 239000010439 graphite Substances 0.000 abstract 1
- 229910002804 graphite Inorganic materials 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 238000013021 overheating Methods 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000008262 pumice Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052567 struvite Inorganic materials 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- C07C45/56—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds
- C07C45/57—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom
- C07C45/58—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom in three-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Catalysts (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE370721D BE370721A (enrdf_load_html_response) | 1929-03-18 | ||
| DEI36997D DE528822C (de) | 1929-02-06 | 1929-02-06 | Verfahren zur Herstellung von Aldehyden |
| GB870929A GB331185A (en) | 1929-03-18 | 1929-03-18 | Improvements in the manufacture and production of aldehydes from 1.2-oxides of hydrocarbons |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB870929A GB331185A (en) | 1929-03-18 | 1929-03-18 | Improvements in the manufacture and production of aldehydes from 1.2-oxides of hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB331185A true GB331185A (en) | 1930-06-18 |
Family
ID=9857730
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB870929A Expired GB331185A (en) | 1929-02-06 | 1929-03-18 | Improvements in the manufacture and production of aldehydes from 1.2-oxides of hydrocarbons |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE370721A (enrdf_load_html_response) |
| GB (1) | GB331185A (enrdf_load_html_response) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2435460A (en) * | 1944-04-20 | 1948-02-03 | Pennsylvania Salt Mfg Co | Process of preparing aldehydic material |
| US2479632A (en) * | 1945-04-16 | 1949-08-23 | Wyandotte Chemicals Corp | Catalytic production of allyl alcohol from propylene oxide |
| US2628255A (en) * | 1951-01-02 | 1953-02-10 | Dow Chemical Co | Production of arylacetaldehydes |
| US3122588A (en) * | 1960-05-31 | 1964-02-25 | Union Carbide Corp | Process for the production of aldehydes |
| US4925986A (en) * | 1989-04-13 | 1990-05-15 | Eastman Kodak Company | Preparation of aldehydes from unsaturated terminal epoxides |
-
0
- BE BE370721D patent/BE370721A/xx unknown
-
1929
- 1929-03-18 GB GB870929A patent/GB331185A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2435460A (en) * | 1944-04-20 | 1948-02-03 | Pennsylvania Salt Mfg Co | Process of preparing aldehydic material |
| US2479632A (en) * | 1945-04-16 | 1949-08-23 | Wyandotte Chemicals Corp | Catalytic production of allyl alcohol from propylene oxide |
| US2628255A (en) * | 1951-01-02 | 1953-02-10 | Dow Chemical Co | Production of arylacetaldehydes |
| US3122588A (en) * | 1960-05-31 | 1964-02-25 | Union Carbide Corp | Process for the production of aldehydes |
| US4925986A (en) * | 1989-04-13 | 1990-05-15 | Eastman Kodak Company | Preparation of aldehydes from unsaturated terminal epoxides |
Also Published As
| Publication number | Publication date |
|---|---|
| BE370721A (enrdf_load_html_response) |
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