Patent Grant
7355062
This invention is comprised in the technical field of catalysts in petrochemistry and in selective oxidation and amoxidation of alkanes and alkenes. It also belongs to the sector of catalysts for processes for obtaining acrylic acid, acrylonitrile and derivatives of these.
Unsaturated α,β carboxylic acids, such as acrylic acid or methacrylic acid are monomers of industrial interest for obtaining synthetic resins and plastics. In general, these acids are obtained through direct oxidation of an olefin (propylene or isobutylene) with oxygen (or air) and high temperatures in the presence of a catalyst. They can also be obtained from unsaturated α,β aldehydes (acrolein or methacrolein) through oxidation in the gaseous phase in the presence of a catalyst.
For economic reasons, it is of industrial interest to substitute olefins by saturated hydrocarbons.
Catalysts based on metal oxides with molybdenum and/or vanadium for the oxidation of propane are described in the U.S. Pat. No. 5,198,580, although the yield of acrylic acid achieved with this type of catalyst is low.
The Mo-V-Te-Nb metal oxides are more effective for selective oxidation of propane to acrylic acid as gathered, for example, from T. Ushikubo et al., U.S. Pat. No. 5380933; EP-608838-B1, M. Lin, M. W. Linsen, EP-A-0962253; S. Komada, H. Hinago, M. Kaneta, M. Watanabe, EP-A-0895809.
The metal oxide system based on Mo—V—Te—Nb—X has also been proposed as an effective system where X can be another chemical element. Thus, in the U.S. Pat. No. 5,380,933 and in the related patent applications EP-0608838, WO-A-98/22421 and WO-A-99/3825, a catalytic system is proposed characterised by their Mo—V—Te—X—O composition, where X is Nb, Ta, W, Ti Al, Zr, Cr, Mn, Fe, Ru, Co, Rh, Ni, Pd, Pt, Sb, Bi, B, In, Ce, and by its crystalline structure defined by an X-ray diffractogram with diffraction angles of 2θ at 22.1, 28.2, 36.2, 45.2, 50.0. The AMNXO system is proposed in the European patent application EP-A-0962253 where A=Mo, W, Fe, Nb, Ta, Zr; M=V, Ce, Cr; N=Te, Bi, Sb, Se; X=Nb, Ta, W, Ti, Al, Zr, Cr, Mn, Fe, Ru, Co, Rh, Ni, Pd, Pt, Sb, Bi, B, In, Ce.
These catalysts are similar to others proposed for obtaining acrylonitrile through the amoxidation of propane such as those proposed by T. Ushikubo, K. Oshima, A. Kayo, T. Umezawa, K. Kiyono, I. Sawaki (EP-A-0529853). Likewise, both the type of element proposed and the crystalline structure of the catalytic system are similar to those indicated beforehand for obtaining acrylic acid.
However, the method of preparation and the composition of the conventional catalysts appear to have a great influence on the catalytic properties of these materials (M. M. Lin, Appl. Catal. A 207, 1, 2001; H. Watanabe, Y. Koyasu, Appl. Catal. A 1994-195, 479, 2000). In this sense, the patent EP-A-0962253 refers to a method in the preparation of MoVTeNb catalysts that is different from that proposed in the U.S. Pat. No. 5,380,933 patent and in the related applications for patents EP-0608838, WO-A-98/22421 and WO-A-99/3825.
Also, the Mo—V—Sb—A metal oxides (where A can be Nb, Ta, Sn, W, Ti, Ni, Fe, Cr or Co) appear to be effective in the oxidation of propane to acrylic acid (M Takayashi, X. Tu, T. Hirose, M. Ishii, FR-A-2754817; U.S. Pat. No. 5,994,580). In the case of these catalysts, a selectivity of 72.6% acrylic acid was obtained for a 35% conversion of propane.
The present invention refers to a catalyst for the selective oxidation and amoxidation of alkanes and/or alkenes, particularly in processes for obtaining acrylic acid, acrylonitrile and derivatives of these, whose catalyst, besides Mo, Te, V and at least another A component selected from among Nb, Ta, Se, W, Ti, Fe, Co, Ni, Cr, Ga, Sb, Bi, a rare, alkaline or alkali-earth earth, also comprises Cu, in such a way that at least Mo, Te, V and Cu are present at least in the form of at least an oxide, preferably a mixed calcined oxide, the catalyst presenting in a calcined form, an X-ray diffractogram with five intensive diffraction lines, typically the most intense corresponding to diffraction angles of 2θ at 22.1±0.4, 27.1±0.4; 28.1±0.4, 36.0±0.4 and 45.1±0.4.
In the preferred embodiment, the catalyst has the following empiric formula:
MoTehViCujAkOx
On the other hand, when A is Nb or Ta in this emobodiment, preferably
According to the invention, the catalyst can be a mixed oxide supported on a solid such as, for example, silica, aluminium oxide, titanium oxide and mixtures of these, silica can be present in a proportion of 20 to 70% by weight of the total weight of the catalyst. On the other hand, in its calcined form, the catalyst according to the invention can be in the form of a mixed oxide supported on silicon carbide.
Typically, in its calcined form, the catalyst according to the invention has an X-ray diffractogram whose five most intensive diffraction lines, together with the corresponding intensities relating to the peak of greatest intensity, are those shown in Table 1.
The catalyst in the present invention can be used particularly in
The catalyst in the present invention can be prepared by conventional methods from aqueous solutions of the different elements with the desired atomic relations, and also by employing hydrothermal methods (containing two or more elements in the synthesis, particularly containing Mo and Te). The synthesis temperature and time can be determining. Thus, the synthesis temperature is preferably between 100 and 250° C. and, more precisely, between 150 and 180° C. The synthesis time is, preferably, between 6 and 500 hours, and more precisely between 24 and 200 hours.
The main elements, such as salts, oxides, hydroxides, chlorides or alkoxides can be incorporated pure or as mixtures or two or more elements:
The elements Nb, Ta, Sn, Se, W, Ti, Fe, Co, Ni, Cr, Ga, Sb, Bi, rare earth, alkaline or alkali-earth, can also be incorporated as pure salts, oxides, hydroxides, chlorates or alkoxides, oxalates or mixtures of two or more elements, although they preferably have been incorporated as salts.
Once the different elements have been mixed (either in a solution or by hydro-thermal treatment), the solid is dried and calcined. Drying is performed by conventional methods in a stove, evaporation with stirring, evaporation in a Rotavapor or vacuum drying. The dry solid is calcined in the presence of an inert gas such as, for example, nitrogen, helium, argon or mixtures. Calcination can be carried out by passing a flow of inert gas (with spatial speeds of between 1 and 400 h−1) or static. The temperature is preferably between 350 and 800° C. The calcination time is not determining but is preferred between 0.5 hours and 20 hours. The speed of heating is not determining but is preferred between 0.1° C./minute and 10° C./minute.
Although the catalyst can be used as described in this description, or could also be used supporting it on a solid such as: silica, aluminium oxide, titanium oxide and mixtures of these and also on silicon carbide. In these cases, the fixing of the different catalyst elements on the support can be performed by conventional impregnation methods (pore volume, solution excess) or simply by precipitation of a solution containing the active elements on the support.
This catalyst is particularly active for the selective oxidation and amoxidation of alkanes and/or alkenes. Propane and/or isobutane can be employed as alkanes. Propylene and/or isobutylene as olefins. Pure oxygen, oxygen-inert gas mixtures (with a different proportion of the two) or air enriched with oxygen can be employed as an oxidising agent. The water may be incorporated in the supply in the oxidising process, or not, although, generally, an increase is observed of the selectivity towards acrylic acid when the reaction is carried out in the presence of water vapour. The water content in the reaction mixture can be from 0 at 80% and more preferably between 20 and 60%.
The presence of ammonia and water is required in the amodixation process as well as the gases described for oxidation. The concentration of ammonia in the reaction mixture can be from 2 to 40%, but preferably between 8 and 15%.
Both the oxidation and the amoxidation process can be carried out in a fixed bed reactor or a fluidised bed reactor. The reaction temperature is between 250 and 550° C., preferably between 300 and 480° C., and more preferably between 350 and 440° C. The contact time defined as the ratio between the catalyst volume and the total flow of gases supplied is between 0.001 and 100 s. Although the contact time depends on the method of preparation and the composition of the catalyst employed, in general it is preferable between 0.05 and 50, and more preferably between 0.1 and 25 s.
Aspects of the invention based on some examples will be described below:
120.0 g of tetra-hydrated ammonium hepta-molybdate, 23.80 g of ammonium metavanadate and 35.96 g of telluric acid were dissolved in 1960 ml of hot water at 80° C. obtaining a uniform solution. On the other hand, and after heating to 40° C., a solution (535.2 g) of niobium oxalate was prepared which contained 80.96 millimoles of niobium and added to the previous solution obtaining a solution. The water was removed from this solution with a Rotavapor at 50° C., obtaining a solid. This solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 2 hours in a nitrogen environment.
10.0 g of the calcined solid are added to 10 ml of an aqueous solution with 0.305 g of copper nitrate (II). The solid resulting after the evaporation of the excess water, with stirring at 80° C., was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst. The catalyst presents an X-ray diffractogram as shown in
6.0 g of the catalyst described in example 1 were put in a fixed bed quartz reactor. The oxidation reaction was carried out employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 4 s. The results obtained are shown in table 2.
120.0 g of tetra-hydrated ammonium hepta-molybdate, 23.80 g of ammonium methavanadate and 35.96 g of telluric acid were dissolved in 1960 ml of hot water at 80° C. obtaining a uniform solution. On the other hand, and after heating to 40° C., a solution (535.2 g) of niobium oxalate was prepared which contained 80.96 millimoles of niobium and added to the previous solution obtaining a solution. The water was removed from this solution by evaporation with a Rotavapor at 50° C., obtaining a solid. This solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 2 hours in a nitrogen environment to obtain the catalyst.
12.0 g of the catalyst described in comparative example 1 were put in a fixed bed quartz reactor. The oxidation reaction was carried out employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 9.6 s. The results are shown in table 2. From the results obtained it was shown that the addition of the copper in the composition of the catalyst produces an increase both in the conversion of propane and in the selectivity towards acrylic acid.
120.0 g of tetra-hydrated ammonium hepta-molybdate, 23.80 g of ammonium methavanadate and 35.96 g of telluric acid were dissolved in 1960 ml of hot water at 80° C. obtaining a uniform solution. On the other hand, and after heating to 40° C., a solution (535.2 g) of niobium oxalate was prepared which contained 80.96 millimoles of niobium and added to the previous solution obtaining a solution. The water was removed from this solution by evaporation with a Rotavapor at 50° C. obtaining a solid. This solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 2 hours in a nitrogen environment.
10.0 g of calcined solid were suspended in 10 ml of an aqueous solution with 0.152 g of copper nitrate (II). The water was evaporated with stirring at 800° C. The solid resulting was dried in a stove at 110C for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst.
6.0 g of the calcined solid described in example 1 were put in a fixed bed quartz reactor. The oxidation reaction was carried out employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 9.6 s. The results obtained are shown in table 2. From the results obtained it was shown that the properties of these catalyst systems depend on the quantity of copper incorporated in the catalyst.
120.0 g of tetra-hydrated ammonium hepta-molybdate, 23.80 g of ammonium methavanadate and 35.96 g of telluric acid were dissolved in 1960 ml of hot water at 80° C. obtaining a uniform solution. On the other hand, and after heating to 40° C., a solution (535.2 g) of niobium oxalate was prepared which contained 80.96 millimoles of niobium and added to the previous solution obtaining a solution. The water was removed from this solution by evaporation with a Rotavapor at 50° C. obtaining a solid. This solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 2 hours in a nitrogen environment.
10.0 g of the solid, obtained in the same way as in example 1, were mixed with 10.0 ml of an aqueous solution with 0.458 g of copper nitrate (II). The solid resulting after the evaporation of the excess water. With stirring at 80° C., was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst.
6.0 g of the calcined solid described in example 5 were put in a fixed bed quartz reactor. The oxidation reaction was carried out employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 4 s. The results obtained are shown in table 2.
26.5 g of tetra-hydrated ammonium hepta-molybdate and 5.75 g of telluric acid were dissolved in 195.0 ml of water at 80° C. Ammonium hydroxide was then added (25% aqueous solution) up to pH=7.5. The mixture was stirred and the water left to evaporate. The solid obtained was dried at 80° C.
21.8 g of this solid were suspended in 155.0 g of water at 80° C. and 7.25 g of vanadyl sulphate and 9.05 g of oxalic acid added. The mixture was stirred and transferred to a steel autoclave with an internal lining of Teflon. The autoclave was maintained at 175° C. statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current to obtain the catalyst.
10.0 g of the calcined solid were incorporated in 10.0 ml of an aqueous solution with 0.174 g of copper nitrate (II). Once the water had evaporated, the solid resulting was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst. The X-ray diffractogram of this catalyst is shown in
26.5 g of tetra-hydrated ammonium hepta-molybdate and 5.75 g of telluric acid were dissolved in 195.0 ml of water at 80° C. Ammonium hydroxide was then added (25% aqueous solution) up to pH=7.5. The mixture was stirred and the water left to evaporate. The solid obtained was dried at 80° C.
21.8 g of this solid were suspended in 155.0 g of water at 80° C. and 7.25 g of vanadyl sulphate and 9.05 g of oxalic acid added. The mixture was stirred and transferred to a steel autoclave with an internal lining of teflon. The autoclave was maintained at 175° C. statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current to obtain the catalyst. The X-ray diffractogram of this catalyst is shown in
4.0 g of the catalyst described in example 9 were put in a fixed bed quartz reactor. The oxidation reaction was carried out employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 3.
4.0 g of the catalyst described in example 10 were put in a fixed bed quartz reactor. The oxidation reaction was carried out employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 3
26.5 g of tetra-hydrated ammonium hepta-molybdate and 5.75 g of telluric acid were dissolved in 195.0 ml of water at 80° C. Ammonium hydroxide was then added (25% aqueous solution) up to pH=7.5. The water was evaporated and the resulting solid dried at 80° C., the MT solid being obtained.
30.0 g of the MT solid was suspended in 213.30 g of water at 80° C. and 9.01 g of vanadyl sulphate and 10.39 g of niobium (V) oxalate added. The mixture was stirred and transferred to a steel autoclave with an internal lining of teflon. The autoclave was maintained at 175° C. statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current.
10.0 g of the calcined solid were suspended in 10.0 ml of an aqueous solution with 0.080 g of copper nitrate (II). Once the water had evaporated, the resulting solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst The X-ray diffractogram of this catalyst is shown in
26.5 g of tetra-hydrated ammonium hepta-molybdate and 5.75 g of telluric acid were dissolved in 195.0 ml of water at 80° C. Ammonium hydroxide was then added (25% aqueous solution) up to pH=7.5. In the solution obtained, water was evaporated, with stirring at 80° C. The resulting solid was dried in a stove at 90° C., obtaining the MT solid.
30.0 g of the MT solid were suspended in 213.30 g of water at 80° C. and 9.01 g of vanadyl sulphate and 10.39 g of niobium (V) oxalate were added. The mixture was stirred and transferred to a steel autoclave with an internal teflon cover. The autoclave was kept at 175° C., statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current to obtain the catalyst. This catalyst is characterised by showing an X-ray diffractogram like that shown in
2.5 g of the calcined solid prepared in example 13 were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 3.
2.5 g of the calcined solid prepared in example 14 were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 3. From the results obtained it is shown that the inclusion of the copper in the catalyst increases both the conversion of propane and the selectivity to acrylic acid.
2.5 g of the catalyst described in example 10 were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=3.75:11.25:47.5:30, at a reaction temperature of 400° C. and a contact time of 3.75 s. The results obtained are shown in table 3.
26.5 g of tetra-hydrated ammonium hepta-molybdate and 5.75 g of telluric acid were dissolved in 195.0 g of water at 80° C. Then, ammonium hydroxide (25% aqueous solution) was added up to pH=7.5. The water was evaporated and the resulting solid dried in a stove at 90° C., obtaining the MT solid.
30.0 g of the MT solid were suspended in 213.30 g of water at 80° C. and 9.01 g of vanadyl sulphate and 10.39 g of niobium (V) oxalate were added. The mixture was stirred and transferred to a steel autoclave with an internal teflon cover. The autoclave was kept at 175° C., statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current.
10.0 g of the calcined solid were added to 10.0 ml of aqueous solution with 0.040 g of copper nitrate (II). Once the water had evaporated, the resulting solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst.
2.5 g of the catalyst described in example 10 were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 3.
2.5 g of the catalyst described in example 18 were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=3:9:38:50, at a reaction temperature of 390° C. and a contact time of 4 s. The results obtained are shown in table 3.
26.5 g of tetra-hydrated ammonium hepta-molybdate and 5.75 g of telluric acid were dissolved in 195.0 g of water at 80° C. Then, ammonium hydroxide (25% aqueous solution) was added up to pH=7.5. The water was evaporated and the resulting solid dried in a stove at 90° C., obtaining the MT solid.
30.0 g of the MT solid was suspended in 213.30 g of water at 80° C. and 9.01 g of vanadyl sulphate and 10.39 g of niobium (V) oxalate were added. The mixture was stirred and transferred to a steel autoclave with an internal teflon cover. The autoclave was kept at 175° C., statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current.
10.0 g of the calcined solid were added to 10.0 ml of aqueous solution with 0.161 g of copper nitrate (II). Once the water had evaporated, the resulting solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst.
2.5 g of the catalyst described in example 10 were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results are shown in table 3. The results obtained show that the catalytic properties of these catalysts depend on the copper contents in the catalyst.
2.5 g of the catalyst described in example 15 were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=3:9:38:50, at a reaction temperature of 390° C. and a contact time of 4.0 s. The results are shown in table 3.
31.80 g of tetra-hydrated ammonium hepta-molybdate and 6.90 g of telluric acid were dissolved in 234.0 g of water at 80° C. Then, ammonium hydroxide (25% aqueous solution) was added up to pH=7.5. The water was evaporated in a Rotavapor at 80° C., obtaining a white solid.
30.0 g of this solid were suspended in 213.30 g of water at 80° C. and 29.9 g of vanadyl sulphate and 15.6 g of niobium (V) oxalate were added. The mixture was stirred and transferred to a steel autoclave with an internal Teflon cover. The autoclave was kept at 175° C., statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current.
14.0 g of the calcined solid in example 11 were added to 14.0 ml of aqueous solution with 0.190 g of copper nitrate (II). Once the water had evaporated, the resulting solid was dried in a stove at 110° C. for 24 hours and ground until it reached particle sizes of less than 0.25 mm. The resulting powder was calcined at 600° C. for 1 hour in a nitrogen environment to obtain the catalyst.
31.80 g of tetra-hydrated ammonium hepta-molybdate and 6.90 g of telluric acid were dissolved in 234.0 g of water at 80° C. Then, ammonium hydroxide (25% aqueous solution) was added up to pH=7.5. The water was evaporated in a Rotavapor at 80° C., obtaining a white solid.
30.0 g of this solid were suspended in 213.30 g of water at 80° C. and 29.9 g of vanadyl sulphate and 15.6 g of niobium (V) oxalate were added. The mixture was stirred and transferred to a steel autoclave with an internal Teflon cover. The autoclave was kept at 175° C., statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current to obtain the catalyst.
2.0 g of the calcined solid were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results are shown in table 4.
2.0 g of the calcined solid were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 4.
20.00 g of tetra-hydrated ammonium hepta-molybdate, 4.34 g of telluric acid and 9.12 g of copper nitrate (II) were dissolved in 180 ml of water at 80° C. The mixture was stirred and, later, the water was left to evaporate. The solid obtained was dried at 100° C.
16.24 g of this solid were suspended in 106.65 g of water at 80° C. and 4.51 g of vanadyl sulphate and 5.19 g of niobium (V) oxalate were added. The mixture was stirred and transferred to a steel autoclave with an internal Teflon cover. The autoclave was kept at 175° C., statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current to obtain the catalyst.
2.0 g of this solid were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 4.
10.00 g of tetra-hydrated ammonium hepta-molybdate, 2.17 g of telluric acid and 4.56 g of copper nitrate (II) were dissolved in 90 ml of water at 80° C. The mixture was left to evaporate while stirring at 80° C. The solid obtained was dried at 100° C. for 16 hours. A turquoise green coloured solid was obtained that was denominated solid A.
10.60 g of tetra-hydrated ammonium hepta-molybdate and 2.30 g of telluric acid were dissolved in 78.00 g of water at 80° C. Then, ammonium hydroxide (25% aqueous solution) was added up to pH=7.5, stirred for 1 hour and left to evaporate, while stirring at 80° C. The solid obtained was dried at 80° C. for 16 hours, obtaining a white solid that was denominated solid B.
2.72 g of solid A and 12.56 g of solid B were suspended in 106.65 g of water at 80° C. and 4.91 g of vanadyl sulphate and 5.19 g of niobium (V) oxalate were added. The mixture was stirred and transferred to a steel autoclave with an internal Teflon cover. The autoclave was kept at 175° C., statically, for 2 days. The contents of the autoclave were filtered, washed with distilled water and dried at 80° C. The solid obtained was calcined at 600° C. for 2 hours in a nitrogen current to obtain the catalyst. The calcined compound shows an Mo1.0Te0.17V0.3Nb0.12Cu0.05On stoichiometry with an X-ray diffractogram like that shown in
2.0 g of this solid were put in a fixed bed quartz reactor. The reaction took place employing a mixture of gases, with a molar relation of propane: oxygen: helium: water=4:8:58:30, at a reaction temperature of 380° C. and a contact time of 1.6 s. The results obtained are shown in table 4.
1.5 g of the catalyst described in example 13 was put in a fixed bed quartz reactor. The reaction was carried out employing a mixture of gases, with a molar relation of propylene: oxygen: helium: water=2:8:80:10, at a reaction temperature of 380° C. and a contact time of 0.1 s. The results are shown in table 4.
1.5 g of the catalyst of example 14 was put in a fixed bed quartz reactor. The reaction was carried out employing a mixture of gases, with a molar relation of propylene: oxygen: helium: water=2:8:80:10, at a reaction temperature of 380° C. and a contact time of 0.2 s. The results are shown in table 5.
2.5 g of the catalyst of example 13 were put in a fixed bed quartz reactor. The reaction was carried out employing a mixture of gases, with a molar relation of propylene: oxygen: helium: water=2:8:80:10, at a reaction temperature of 380° C. and a contact time of 0.8 s. The results are shown in table 5.
1AA = Acrylic Acid
1AA = Acrylic Acid
1AA = Acrylic Acid
1AA = Acrylic Acid
| Number | Date | Country | Kind |
|---|---|---|---|
| 200101756 | Jul 2001 | ES | national |
The present application is a Continuation of co-pending PCT Application No. PCT/ES02/00357, filed Jul. 16, 2002, which in turn, claims priority from Spanish Application Serial No. 200101756, filed Jul. 17, 2001. Applicants claim the benefits of 35 U.S.C. §120 as to the PCT application and priority under 35 U.S.C. §119 as to said Spanish application, and the entire disclosures of both applications are incorporated herein by reference in their entireties.
| Number | Name | Date | Kind |
|---|---|---|---|
| 5198580 | Bartek et al. | Mar 1993 | A |
| 5380933 | Ushikubo et al. | Jan 1995 | A |
| 5994580 | Takahashi et al. | Nov 1999 | A |
| Number | Date | Country |
|---|---|---|
| 0 031 693 | Jul 1981 | EP |
| 0 489506 | Jun 1992 | EP |
| 0529853 | Aug 1992 | EP |
| 0608838 | Jan 1994 | EP |
| 0895809 | Aug 1998 | EP |
| 0962253 | May 1999 | EP |
| 0 962 253 | Dec 1999 | EP |
| 0 970942 | Jan 2000 | EP |
| 0 997454 | May 2000 | EP |
| 2 061 572 | Dec 1994 | ES |
| 2 754 817 | Oct 1997 | FR |
| PCTJP9704169 | Nov 1997 | WO |
| PCTJP9803151 | Jul 1998 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20040230070 A1 | Nov 2004 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/ES02/00357 | Jul 2002 | US |
| Child | 10759384 | US |
