FR2420520A1 - Propylene oxide and acetic acid prodn. - from propylene and acetaldehyde by oxidn. over boride catalyst (CS 29.12.78) - Google Patents
Propylene oxide and acetic acid prodn. - from propylene and acetaldehyde by oxidn. over boride catalyst (CS 29.12.78)Info
- Publication number
- FR2420520A1 FR2420520A1 FR7808666A FR7808666A FR2420520A1 FR 2420520 A1 FR2420520 A1 FR 2420520A1 FR 7808666 A FR7808666 A FR 7808666A FR 7808666 A FR7808666 A FR 7808666A FR 2420520 A1 FR2420520 A1 FR 2420520A1
- Authority
- FR
- France
- Prior art keywords
- propylene
- acetaldehyde
- catalyst
- acetic acid
- oxidn
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/04—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen
- C07D301/06—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen in the liquid phase
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/23—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
- C07C51/235—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups
-
- 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)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Prodn. of propylene oxide (I) and acetic acid (II) comprises liq. phase oxidn. of propylene and acetaldehyde with an O2 contg. gas at 70-100 degrees C. and 40-50 atmos., in presence of a boride of Ta, Mo, Zr or N as catalyst. The catalyst is pref. 0.1-0.2 wt.% on the reaction mixt. Prods. are intermediates for polymers, synthetic fibres and solvents. The catalysts increase selectivity of (I) prodn. from acetaldehyde, e.g. to 93 mole %. Pref. a reactor is charged with catalyst and starting materials, brought to temp. and pressure (esp. 70-80 degrees. and 40 atmos.), then a gas contg. 10-100 vol.% O2 passed through. Reaction is esp. for 1-1.5 hr. and prods. are recovered by fractional distn.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7808666A FR2420520A1 (en) | 1978-03-24 | 1978-03-24 | Propylene oxide and acetic acid prodn. - from propylene and acetaldehyde by oxidn. over boride catalyst (CS 29.12.78) |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7808666A FR2420520A1 (en) | 1978-03-24 | 1978-03-24 | Propylene oxide and acetic acid prodn. - from propylene and acetaldehyde by oxidn. over boride catalyst (CS 29.12.78) |
Publications (1)
Publication Number | Publication Date |
---|---|
FR2420520A1 true FR2420520A1 (en) | 1979-10-19 |
Family
ID=9206269
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7808666A Pending FR2420520A1 (en) | 1978-03-24 | 1978-03-24 | Propylene oxide and acetic acid prodn. - from propylene and acetaldehyde by oxidn. over boride catalyst (CS 29.12.78) |
Country Status (1)
Country | Link |
---|---|
FR (1) | FR2420520A1 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1293960A (en) * | 1961-06-30 | 1962-05-18 | Edison Soc | Process for the production of oxygenates by direct catalytic oxidation of lower olefins |
SU558915A1 (en) * | 1974-12-16 | 1977-05-25 | Предприятие П/Я А-1748 | The method of producing olefin oxides with - with |
-
1978
- 1978-03-24 FR FR7808666A patent/FR2420520A1/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1293960A (en) * | 1961-06-30 | 1962-05-18 | Edison Soc | Process for the production of oxygenates by direct catalytic oxidation of lower olefins |
SU558915A1 (en) * | 1974-12-16 | 1977-05-25 | Предприятие П/Я А-1748 | The method of producing olefin oxides with - with |
Non-Patent Citations (1)
Title |
---|
CA1978 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3350422A (en) | Catalytic epoxidation of an olefinically unsaturated compound using an organic hydroperoxide as an epoxidizing agent | |
GB983677A (en) | A process for the preparation of terephthalic acid having extremely high purity | |
US3436409A (en) | Epoxidation process | |
ES460492A1 (en) | High yield, low byproduct alpha , beta -unsaturated aldehydes from olefins | |
US4124600A (en) | Preparation of tetrahydrofuran | |
US3194843A (en) | Reactivation of catalyst in production of a phenol | |
FR2420520A1 (en) | Propylene oxide and acetic acid prodn. - from propylene and acetaldehyde by oxidn. over boride catalyst (CS 29.12.78) | |
US3634464A (en) | Olefin epoxidation | |
GB1029175A (en) | Process for the preparation of carbonyl compounds | |
ES8400421A1 (en) | Process for the preparation of epsilon-caprolactone. | |
US4012424A (en) | Cracking of mixtures containing hydroxyesters | |
GB1488890A (en) | Catalyst with mo,v,ti and process for preparing unsaturated acids | |
GB1015003A (en) | Production of ketones | |
US3523956A (en) | Process for preparing oxirane compound | |
US4256650A (en) | Process for preparing propylene oxide and acetic acid | |
Yamanaka et al. | Epoxidation of Alkenes with O2 Catalyzed by EuCl3 under Ambient Conditions. | |
GB2008593A (en) | Process for the preparation of epoxides | |
US3564018A (en) | Production of lactones having from six to thirteen ring members and isobutyric acid | |
US4456555A (en) | Manufacture of aryl esters | |
US3914291A (en) | Process for splitting cycloaliphatic hydroperoxides | |
GB1115186A (en) | Epoxidation process | |
US2027378A (en) | Method of converting alcohols to acids | |
ES8202325A1 (en) | Process for recovering and reactivating catalysts that contain cobalt used in the conversion of olefins with carbon monoxide and alkanols. | |
US3843694A (en) | Catalytic epoxidation of olefins | |
US3235619A (en) | Production of conjugated diolefines |