# US 4,400,568 A · Process for preparing styrene, and an appropriate agent

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- Number: US 4,400,568 A
- Document ID: US4400568A
- Status: Granted
- Kind: A
- Application number: 06/368,920
- Filed: 1982-04-16
- Granted: 1983-08-23
- Earliest claimed: 1982-04-16
- Assignees: Hanns Hofmann; Gerd Emig; Wolfgang Ruppert
- Inventors: Hanns Hofmann; Gerd Emig; Wolfgang Ruppert
- Web page: https://patentgrep.com/patent/US4400568A

## CPC

- B01J 27/16: containing oxygen {, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr}
- C07C 5/48: with oxygen as an acceptor
- B01J: CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS

## Abstract

The invention relates to a process for oxidatively dehydrogenating dehydrogenatable organic compounds to prepare styrene. In this process, the compounds mentioned are reacted in the vapor phase with oxygen at a temperature above 350.degree. C. in the presence of a catalyst based on zirconium phosphate. Suitable dehydrogenatable organic compounds are above all saturated alkylaromatics, in particular ethylbenzene.

## Claims

### Claim 1

A process for oxidatively dehydrogenating ethylbenzene to prepare styrene, which process comprises reacting ethylbenzene in the vapor phase with oxygen at a temperature above 350.degree. C. in the presence of a crystalline zirconium phosphate catalyst capable of ion exchange, said zirconium phosphate catalysts having been precipitated in a gel-like form from a zirconium salt solution by the addition of an excess of phosphate ions, impregnated with at least 1 liter of an at least 10 M orthosphophoric acid per 100 g of zirconium phosphate gel, filtered off from excess phosphoric acid, washed with water until the water draining off has a pH of 2 to 3 and dried at 120.degree. to 250.degree. C.

### Claim 2 (depends on 1)

The process as claimed in claim 1, wherein a mixture of an oxygen-containing gas and ethylbenzene is passed over the catalyst at a temperature of 350.degree. C.-550.degree. C. and a residence time of 0.5 to 5 grams of gas mixture per gram of catalyst per hour.

### Claim 3 (depends on 2)

The process as claimed in claim 2, wherein the ethylbenzene is diluted with an up to 10-fold amount of inert gas.

### Claim 4 (depends on 1)

The process as claimed in claim 1, wherein the temperature is about 380.degree. C. to 530.degree. C.

### Claim 5 (depends on 1)

The process as claimed in claim 1, wherein the molar ratio of oxygen ethylbenzene is 0.5:1 to 2:1.

### Claim 6 (depends on 1)

The process as claimed in claim 1, wherein the catalyst is subjected to an impregnating period of 10 to 14 hours at about the boiling point and to 30-40 hours at room temperature and to a drying period of 24-48 hours.

### Claim 7 (depends on 1)

The process as claimed in claim 1, wherein Cs ions are added before the impregnating step and drying step.

### Claim 8 (depends on 1)

The process as claimed in claim 1, wherein the catalyst has a surface area of 10-50 m.sup.2 /g.

### Claim 9 (depends on 1)

The process as claimed in claim 1, wherein the regeneration of the catalyst, when necessary, is carried out by incompletely burning off the carbon-containing deposits at 400.degree.-540.degree. C. down to a residual content of 7-15% by weight by means of oxygen or gases which contain molecular oxygen.

### Claim 10 (depends on 1)

The process as claimed in claim 1, wherein the catalyst further contains ions of an element from the group Ia, IIa, IVb, Vb, VIb, VIIb or VIII of the periodic system of the elements.

### Claim 11 (depends on 10)

The process as claimed in claim 10, wherein the ions are contained in the catalyst in a concentration of 1-20% by weight.

### Claim 12 (depends on 10)

The process as claimed in claim 10, wherein the ions are taken from the group of K, Cs, Mg, Ba, Cr, Mn, Fe or Ni ions.

### Claim 13 (depends on 10)

The process as claimed in claim 10, wherein the ions are taken from the group of K, Cs, Ba, Fe, or Ni ions.

### Claim 14 (depends on 10)

The process as claimed in claim 10, wherein the ions are taken from the group of K, Cs, Mg, Cr, Mn, Fe or Ni ions.