초록 ▼

Catalytically active multielement oxide materials which contain at least one of the elements Nb and W and the elements Mo, V and Cu are prepared by a process in which an intimate dry blend containing ammonium ions is prepared and said dry blend is subjected to a thermal treatment in an atmosphere ha

Catalytically active multielement oxide materials which contain at least one of the elements Nb and W and the elements Mo, V and Cu are prepared by a process in which an intimate dry blend containing ammonium ions is prepared and said dry blend is subjected to a thermal treatment in an atmosphere having a low molecular oxygen content at elevated temperatures, a portion of the ammonium ions contained in the intimate dry blend being decomposed with liberation of ammonia and the oxygen content of the thermal treatment atmosphere being increased in the course of the thermal treatment.

대표청구항 ▼

We claim: 1. A process for the preparation of a catalytically active multimetal oxide comprising material which comprises at least one of the elements Nb and W, and the elements Mo, V and Cu, wherein the molar fraction of the element Mo, based on the total amount of all elements other than oxygen i

We claim: 1. A process for the preparation of a catalytically active multimetal oxide comprising material which comprises at least one of the elements Nb and W, and the elements Mo, V and Cu, wherein the molar fraction of the element Mo, based on the total amount of all elements other than oxygen in the catalytically active multimetal oxide comprising material, is from 20 to 80 mol %, wherein the molar ratio of Mo to V, Mo/V, is from 15:1 to 1:1, wherein the corresponding molar ratio Mo/Cu is from 30:1 to 1:3 and the corresponding molar ratio Mo/(total amount of W and Nb) is from 80:1 to 1:4, the process comprising preparing an intimate dry blend comprising ammonium ions from starting compounds that comprise the elemental constituents of the multimetal oxide comprising material, other than oxygen, as components; and thermally treating the intimate dry blend at elevated temperatures in an atmosphere A having a low content of molecular oxygen, so that at least a portion of the ammonium ions contained in the intimate dry blend are decomposed at ≧160° C. with liberation of ammonia, wherein the thermal treatment is carried out as follows: heating the intimate dry blend at a heating rate of ≦10° C./min to a decomposition temperature in a decomposition temperature range of from 240° C. to 360° C., and then keeping the temperature in the decomposition range until at least 90 mol % of the total amount MA of ammonia liberated altogether in the entire course of the thermal treatment of the intimate dry blend from the intimate dry blend at above 160° C. has been liberated; reducing, to less than or equal to 0.5% by volume, the content of molecular oxygen in the atmosphere A in which the thermal treatment of the intimate dry blend takes place no later than when the intimate dry blend has reached 230° C., and maintaining the reduced oxygen content until at least 20 mol % of the total amount MA of ammonia liberated altogether in the entire course of the thermal treatment has been liberated; taking the intimate blend out of the decomposition temperature range, at a rate of ≦10° C./min, and into a calcination temperature range of from 380 to 450° C. no earlier than when ≧70 mol % of the total amount of MA of ammonia liberated altogether in the entire course of the thermal treatment has been liberated increasing the content of molecular oxygen in the atmosphere A to >0.5 to 4% by volume no later than when 98 mol % of the total amount MA of ammonia liberated altogether in the entire course of the thermal treatment has been liberated and calcining the intimate dry blend at this increased oxygen content of the atmosphere A in the calcination temperature range. 2. The process as claimed in claim 1, wherein the content of ammonium ions in the intimate dry blend, prior to the thermally treating step, is ≧5 mol %, based on the total molar content of elemental constituents of the subsequent catalytically active multimetal oxide comprising material, other than oxygen, in the intimate dry blend. 3. The process as claimed in claim 1 or 2, wherein the temperature rate at which the intimate dry blend is heated to the decomposition temperature is ≦5° C./min. 4. The process of claim 1, wherein the temperature rate at which the intimate dry blend is heated to the decomposition temperature is ≦3° C./min. 5. The process of claim 1, wherein the decomposition temperature range is from 300 to 350° C. 6. The process of claim 1, wherein the intimate dry blend is kept in the decomposition temperature range until at least 95 mol % of the total amount MA of ammonia liberated altogether in the entire course of the thermal treatment of the intimate dry blend from the intimate dry blend at above 160° C. has been liberated. 7. The process of claim 1, wherein the content of molecular oxygen in the atmosphere A is ≦0.3% by volume no later than when the intimate dry blend has reached 230° C. 8. The process of claim 1, wherein the content of molecular oxygen in the atmosphere A is increased to >0.5 to 4% by volume before 80 mol % of the total amount MA of ammonia liberated altogether in the entire course of the thermal treatment has been liberated. 9. The process of claim 1, wherein the content of molecular oxygen in the atmosphere A is increased to 0.6 to 4% by volume no later than when 98 mol % of the total amount MA of ammonia liberated altogether in the entire course of the thermal treatment has been liberated. 10. The process of claim 1, wherein the content of molecular oxygen in the atmosphere A is increased to 1 to 3% by volume no later than when 98 mol % of the total amount MA of ammonia liberated altogether in the entire course of the thermal treatment has been liberated. 11. The process of claim 1, wherein the calcination temperature range is from 380 to 430° C. 12. The process of claim 1, wherein, after calcination is complete, the intimate dry blend is cooled to ≦100° C. in the course of a period of ≦5 hours. 13. The process as claimed in claim 12, wherein the cooling is effected to at least 350° C. in an atmosphere A whose content of molecular oxygen is ≦5% by volume. 14. The process of claim 1, wherein the ammonia content of the atmosphere A passes through a maximum which is ≦10% by volume in the course of the thermal treatment. 15. The process as claimed in claim 14, wherein the atmosphere A reaches its maximum ammonia content before the intimate dry blend has reached the calcination temperature range. 16. The process of claim 1, wherein the catalytically active multimetal oxide comprising material satisfies the stoichiometry I Mo12VaX1bX2c X3dX4eX5fX6 gOn (I), wherein: X1 is W, Nb, Ta, Cr and/or Ce, X2 is Cu, Ni, Co, Fe, Mn and/or Zn, X3 is Sb and/or Bi, X4 is one or more alkali metals, X5 is one or more alkaline earth metals, X6 is Si, Al, Ti and/or Zr, a is from 1 to 6, b is from 0.2 to 4, c is from 0.5 to 18, d is from 0 to 40, e is from 0 to 2, f is from 0 to 4, g is from 0 to 40 and n is a number which is determined by the valency and frequency of the elements other than oxygen in I. 17. The process of claim 1, wherein the catalytically active multimetal oxide comprising material is one of the formula III [A]p[B]q[C]r (III) wherein: A is Mo12VaX1bX2cX3 dX4eX5fX6g Ox, B is X71CuhHiOy C is X81SbjHkOz, X1 is W, Nb, Ta, Cr and/or Ce, X2 is Cu, Ni, Co, Fe, Mn and/or Zn, X3 is Sb and/or Bi, X4 is Li, Na, K, Rb, Cs and/or H, X5 is Mg, Ca, Sr and/or Ba, X6 is Si, Al, Ti and/or Zr, X7 is Mo, W, V Nb and/or Ta, X8 is Cu, Ni, Zn, Co, Fe, Cd, Mn, Mg, Co, Sr and/or Ba, a is from 1 to 8, b is from 0.2 to 5, c is from 0 to 23, d is from 0 to 50, e is from 0 to 2, f is from 0 to 5, g is from 0 to 50, h is from 0.3 to 2.5 i is from 0 to 2, j is from 0.1 to 50, k is from 0 to 50, x, y and z are numbers which are determined by the valency and frequency of the elements other than oxygen in A, B and C, p and q are positive numbers and r is 0 or a positive number, the ratio p/(q+r) being from 20:1 to 1:20 and, where r is a positive number, the ratio q/r being from 20:1 to 1:20, which contains the moiety [A]p in the form of three-dimensional regions A having the chemical composition A: Mo12VaX1bX2cX3 dX4eX4fX6g Ox, the moiety [B]q in the form of three-dimensional regions B having the chemical composition B: X71CuhHiOy and the optional moiety [C]r in the form of three-dimensional regions C having the chemical composition C: X81SbjHkOz, the regions A, B and, if desired, C being distributed relative to one another as in a mixture of finely divided A, finely divided B and, if desired, finely divided C. 18. The process of claim 1, wherein the thermal treatment is carried out in a rotary tube furnace through which a gas stream flows. 19. The process as claimed in claim 18, wherein the rotary tube furnace is operated batchwise. 20. The process as claimed in claim 18 or 19, wherein at least a portion of the gas stream running through the rotary tube is circulated. 21. The process as claimed in claim 18 or 19, wherein the pressure of the gas stream flowing through the rotary tube on leaving the rotary tube is below the ambient pressure of the rotary tube.