Claims
- 1. A process for the preparation of a carboxylic anhydride comprising reacting a hydrocarbon with molecular oxygen in the vapor phase, in the presence of a solid oxidation catalyst, said solid oxidation catalyst being obtained by the steps of:
- (a) forming a catalyst precursor by depositing on titanium dioxide catalyst solids in the anatase form, a continuous monolayer amount of at least one titanium oxide source which is convertible to titanium oxide upon calcining and titanium oxide source is deposited on said titanium dioxide catalyst solids in an amount sufficient to provide about 0.1 to 10 wt. % of titanium oxides, calculated as TiO.sub.2, deposited on the titanium dioxide solids wherein the mole ratio of titanium present as a monolayer on the titanium dioxide catalyst solids to the titanium in the titanium dioxide solids is from about 0.0001 to about 0.111;
- (b) calcining said catalyst precursor under conditions sufficient to convert at least a portion of said titanium oxide source into titanium oxide;
- (c) depositing upon the calcined catalyst precursor at least a continuous monolayer amount of at least one vanadium oxide source which is convertible to vanadium oxide upon calcining;
- (d) calcining the catalyst solids formed in step (c) under conditions sufficient to convert at least a portion of said vanadium oxide source to vanadium oxide, said catalyst containing from about 0.7 to 50 wt. % vanadium oxides, calculated as V.sub.2 O.sub.5 and the mole ratio of vanadium to titanium present in the calcined catalyst is from about 0.003 to 0.44 gram atoms of vanadium per gram atom of titanium.
- 2. The process according to claim 1 wherein said catalyst precursor is calcined in step (b) at a temperature of from about 150.degree. to 750.degree. C.
- 3. The process according to claim 2 wherein said calcining is effected for a time of from about 0.5 to 16 hours.
- 4. The process according to claim 1 wherein said vanadium oxide source comprises at least one member selected from the group consisting of vanadium halides, phosphates, oxides, carbonates, sulfates, alkoxides, nitrates, hydroxides, carboxylates and oxy halides.
- 5. The process according to claim 4 wherein said vanadium oxide source comprises at least one compound selected from the group consisting of vanadium pentoxide, ammonium metavanadate, vanadyl sulfate, vanadyl chloride, vanadyl dichloride, metavanatic acid, pyrovanatic acid, vanadium hydroxide, vanadyl oxalate and vanadyl carboxylates.
- 6. The process according to claim 1 wherein said catalyst, following calcination according to step (d), is characterized by a specific surface area of less than 50 square meters per gram.
- 7. The process according to claim 1 wherein said hydrocarbon comprises at least one member selected from the group consisting of orthoxylene and naphthalene, and wherein said carboxylic anhydride comprises phthalic anhydride.
- 8. The process according to claim 7 wherein said orthoxylene or naphthalene feed is passed to a reaction zone containing said solid oxidation catalyst at a mass flow rate of from about 20 to 150 grams per Nm.sup.3 of air under vapor phase conditions, said reaction being effected at a temperature of from about 200.degree. to 500.degree. C.
- 9. The process according to claim 1 wherein said hydrocarbon comprises durene and wherein said carboxylic anhydride comprises pyromellitic dianhydride.
- 10. The process according to claim 9 wherein said durene is passed to a reaction zone containing said solid oxidation catalyst under the vapor phase reaction conditions and at a durene feed rate of from about 5 to 100 grams per Nm.sup.3 of air, and said reaction is effected at a temperature within the range of from about 200.degree. to 500.degree. C.
- 11. The process according to claim 1 wherein said vanadium oxide source is deposited upon said calcined catalyst precursor in an amount sufficient to provide at least N.sub.min grams of V.sub.2 O.sub.5, wherein
- N.sub.min =(G).times.(A).times.(0.0007)
- wherein "G" is the grams of said calcined catalyst precursor and "A" is the specific surface area of said calcined catalyst precursor.
- 12. The process according to claim 11 wherein said vanadium oxide source is deposited on said calcined catalyst precursor in an amount sufficient to provide at least about 1.7 N.sub.min grams of V.sub.2 O.sub.5.
CROSS-REFERENCE TO RELATED APPLICATION
This application is a continuation-in-part of pending application Ser. No. 102,164, filed Sept. 28, 1987, which is a divisional application of Ser. No. 782,966 filed Oct. 2, 1985, which issued as U.S. Pat. No. 4,728,744.
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Divisions (1)
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Number |
Date |
Country |
Parent |
782966 |
Oct 1985 |
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Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
102164 |
Sep 1987 |
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