Claims
- 1. An arsenic-resistant catalyst, comprising at least the metals vanadium and molybdenum in an oxygen lattice, having at least one relatively lower-oxygen phase obtained by reduction-treating of a relatively higher-oxygen phase of a general formula V.sub.x Mo.sub.y O.sub.32 in a given structure, where x+y.ltoreq.12 and where x.gtoreq.1 and y.gtoreq.1, and a partly reduced molybdenum oxide phase, wherein said relatively lower-oxygen phase has said given structure.
- 2. The arsenic-resistant catalyst according to claim 1, including a support material to which said phases are applied.
- 3. The arsenic-resistant catalyst according to claim 1, including an oxidic support to which said composite oxides are applied, said oxides having pores with a pore radius of over 200 angstrom units for more than 75% of said pores.
- 4. The arsenic-resistant catalyst according to claim 1, wherein said catalyst has pores with over 70% of said pores having a radius of from 200 to 10,000 angstrom units.
- 5. The arsenic-resistant catalyst according to claim 1, wherein said catalyst has pores with more than 70% of said pores having a pore radius of over 500 angstrom units.
- 6. The arsenic-resistant catalyst according to claim 1, wherein said catalyst has pores with more than 15% of said pores having a pore radius of over 1000 angstrom units.
- 7. The arsenic-resistant catalyst according to claim 1, including an oxidic support for said phases having at least one material selected from the group consisting of titanium oxide, codierite, alumina and silica.
- 8. The arsenic-resistant catalyst according to claim 1, including a metal support for said phases catalyst being formed of a material selected from the group consisting of expanded sheet metal, corrugated sheet metal and metal trellis work.
- 9. The arsenic-resistant catalyst according to claim 1, including a support for said phases being formed of swelling clay.
- 10. An arsenic-resistant catalyst, comprising at least the elements vanadium and molybdenum, having at least one relatively lower-oxide phase with a general formula V.sub.x Mo.sub.y O.sub.32 produced by mixing at least precursors of vanadium oxide and molybdenum oxide with one another to form a mixture, where x+y.ltoreq.12 and where x.gtoreq.1 and y.gtoreq.1, heating the mixture to a temperature at which at least one relatively higher-oxide phase with a general formula V.sub.x Mo.sub.y O.sub.32 in a given structure is formed, then cooling down the mixture and subjecting said phase to a reducing treatment to prepare the lower-oxygen phase in said given structure, and a patly reduced molybdenum oxide phase.
- 11. The catalyst according to claim 10, including an oxidic support for said phases having at least one material selected from the group consisting of titanium oxide, cordierite, alumina and silica.
- 12. A method for producing an arsenic-resistant catalyst, which comprises mixing at least precursors of vanadium oxide and molybdenum oxide with one another to form a mixture, heating the mixture to a temperature at which at least one relatively oxygen-rich phase with a general formula V.sub.x Mo.sub.y O.sub.32 in a given structure is formed, where x+y.ltoreq.12 and where x.gtoreq.1 and y.gtoreq.1, then cooling down the mixture, and then subjecting the relatively oxygen-rich phase to a reducing treatment to prepare a relatively lower-oxygen phase with said given structure.
- 13. The method according to claim 12, which comprises mixing vanadium oxide and molybdenum oxide with one another in the mixing step.
- 14. The method according to claim 12, which comprises heating the mixture until it is in completely molten form in the heating step.
- 15. The method according to claim 12, which comprises heating the mixture to above 600.degree. C. in the heating step.
- 16. The method according to claim 12, which comprises applying the lower-oxygen phase of the general formula V.sub.x Mo.sub.y O.sub.32 to a metal support.
- 17. The method according to claim 12, which comprises mixing the lower-oxygen phase of the general formula V.sub.x Mo.sub.y O.sub.32 in powder form with an oxidic support material.
- 18. The method according to claim 17, which comprises calcining the lower-oxygen phase of the general formula V.sub.x Mo.sub.y O.sub.32 at substantially from 500.degree. C. to 600.degree. C.
- 19. The method according to claim 13, which comprises mixing vanadium oxide and molybdenum oxide with one another in a ratio of about 0.7:1 in the mixing step.
- 20. The method according to claim 12, which comprises melting the mixture at melting temperatures of substantially above 600.degree. C., and maintaining the melting temperatures for approximately half an hour.
- 21. The method according to claim 12, which comprises after the cooling down step, grinding down the V.sub.x Mo.sub.y O.sub.32 phase to a particle diameter of substantially less than 180 .mu.m, and then performing a reducing treatment to form a lower-oxygen phase of the general formula V.sub.x Mo.sub.y O.sub.32.
- 22. The method according to claim 12, which comprises grinding down the V.sub.x Mo.sub.y O.sub.32 phase to a particle diameter of substantially less than 180 .mu.m, and performing a gas reduction at substantially from 400.degree. C. to 590.degree. C. in a fixed bed.
- 23. The method according to claim 12, which comprises grinding down the V.sub.x Mo.sub.y O.sub.32 phase to a particle diameter of substantially less than 180 .mu.m, and performing a gas reduction with a reducing gas at substantially from 400.degree. C. to 590.degree. C. in a fluidized bed.
- 24. The method according to claim 12, which comprises adding arsenous oxide as a reducing agent during the reducing treatment.
- 25. The method according to claim 12, which comprises adding at least one gas selected from the group consisting of methane, carbon monoxide, hydrogen, hydrocarbons and aromatic compounds as a reducing agent during the reducing treatment.
- 26. The method according to claim 12, which comprises adding arsenous oxide as a reducing agent during the reducing treatment, and leaching excess arsenic out of the lower-oxygen V.sub.x Mo.sub.y O.sub.32 product, after the reducing treatment.
- 27. The method according to claim 12, which comprises adding arsenous oxide as a reducing agent during the reducing treatment, and removing excess arsenic from the lower-oxygen V.sub.x Mo.sub.y O.sub.32 product by heating, after the reducing treatment.
- 28. The method according to claim 12, which comprises grinding down the V.sub.x Mo.sub.y O.sub.32 phase to a particle diameter of substantially less than 180 .mu.m, and performing an electro-reduction to form the lower-oxygen phase of the same structure.
- 29. The method according to claim 12, which comprises grinding down the V.sub.x Mo.sub.y O.sub.32 phase to a particle diameter of substantially less than 180 .mu.m, and tempering for several hours, in dependence on a degree of conversion, in a vacuum below the melting point.
- 30. The method according to claim 12, which comprises performing the reducing treatment step by gas reduction in the V.sub.x Mo.sub.y O.sub.32 phase in a completely molten form at a temperature above 600.degree. C., in the presence of at least one reducing agent selected form the group consisting of arsenous oxide, carbon monoxide, hydrogen, methane, other hydrocarbons and aromatic compounds.
- 31. The method according to claim 12, which comprises performing the reducing treatment step by electroreduction of the V.sub.x Mo.sub.y O.sub.32 phase in completely molten form at a temperature above 600.degree. C.
- 32. The method according to claim 28, which comprises performing the reducing treatment step by electroreduction of the V.sub.x Mo.sub.y O.sub.32 phase in completely molten form at a temperature above 600.degree. C.
- 33. The method according to claim 17, which comprises obtaining the lower-oxygen V.sub.x Mo.sub.y O.sub.32 phase by the reducing treatment of the V.sub.x Mo.sub.y O.sub.32 phase in molten form, and grinding down to substantially less than 180 .mu.m after cooling down and before mixing with the oxidic support.
- 34. The method according to claim 30, which comprises obtaining the lower-oxygen V.sub.x Mo.sub.y O.sub.32 phase by the reducing treatment of the V.sub.x Mo.sub.y O.sub.32 phase in molten form, and grinding down to substantially less than 180 .mu.m after cooling down and before mixing with an oxidic support.
- 35. The method according to claim 12, which comprises applying the lower-oxygen V.sub.x Mo.sub.y O.sub.32 phase to a titanium oxide support having a BET surface area of substantially from 40 to 200 m.sup.2 /g and a pore radius of substantially from 20 to 200 angstrom units.
Priority Claims (2)
Number |
Date |
Country |
Kind |
4025174 |
Aug 1990 |
DEX |
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91 107 327.9 |
May 1991 |
EPX |
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CROSS-REFERENCE TO RELATED APPLICATION
This application is a continuation-in-part of application Ser. No. 740,813, filed Aug. 6, 1991, abandoned.
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Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
740813 |
Aug 1991 |
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