USRE30642EExpiredUtility

Process for preparing molybdenum acid salts

Priority: Jan 23, 1980Filed: Jan 23, 1980Granted: Jun 9, 1981
Est. expiryJan 23, 2000(expired)· nominal 20-yr term from priority
B01J 31/04B01J 2231/72C07C 51/412
12
PatentIndex Score
5
Cited by
6
References
9
Claims

Abstract

This invention relates to the preparation of molybdenum acid salts by directly reacting the carboxylic acid with a molybdenum compound while removing the water that is formed. These molybdenum acid salts are useful as catalysts in such processes as in the epoxidation of olefins.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. In a process for preparing a molybdenum carboxylate the improvement which comprises .[.intimately contacting.]. .Iadd.directly reacting .Iaddend.a molybdenum oxide, .[.molybdenum halide,.]. alkali molybdate, alkali earth molybdate, ammonium molybdate, or a mixture of a molybdenum oxide, .[.molybdenum halide,.]. alkali molybdate or alkali earth molybdate and ammonia; with a monocarboxylic acid, at temperatures in the range of 100° to 300° C. while removing water. 
     
     
       2. In a process for preparing a molybdenum carboxylate the improvement which comprises the direct reaction of a molybdenum compound selected from the group consisting of a molybdenum oxide, .[.molybdenum halide,.]. alkali molybdate, alkali earth molybdate and ammonium molybdate; with a monocarboxylic acid, at temperatures in the range 100° to 300° C. while removing water. 
     
     
       3. In a process for preparing a molybdenum carboxylate the improvement which comprises directly reacting a molybdenum compound selected from the group consisting of molybdenum oxide, .[.molybdenum halide,.]. alkali molybdate, alkali earth molybdate and ammonium molybdate; with a monocarboxylic acid selected from the group consisting of mono aliphatic acid, mono alicyclic acid, and mono aromatic acid, at temperatures in the range 100° to 300° C. while removing water azeotropically. 
     
     
       4. The process of claim 3 wherein the molybdenum compound is selected from the group consisting of molybdenum trioxide and ammonium molybdate; the carboxylic acid is selected from the group consisting of a lower aliphatic acid, an intermediate aliphatic acid and a higher aliphatic acid.[.. The.]..Iadd., the .Iaddend.temperature is above 100° C. and the water is removed azeotropically with a compound selected from the group consisting of a lower alkyl benzene, and an alkane. 
     
     
       5. In a process for preparing molybdenum octanoate the improvement which comprises reacting ammonium molybdate with octanoic acid, at temperatures in the range 100° to 300° C. while removing water. 
     
     
       6. A process of claim 5 wherein, the temperature of reaction is 100° C. to 300° C., and the water is removed azeotropically. 
     
     
       7. A process of claim 6, wherein the temperature is between 150° and 250° C., and the water is removed azeotropically with a lower alkyl benzene or an alkane. 
     
     
       8. A process of claim 7, wherein the azeotrope is a lower alkyl benzene. 
     
     
       9. A process of claim 8, wherein the lower alkyl benzene is ethyl benzene.

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