Synthesis and applications of silicate containing Bi
A bismuth silicate and silicon source technology, which is applied in chemical instruments and methods, physical/chemical process catalysts, chemical/physical processes, etc., can solve problems that do not involve pure bismuth silicate, and achieve good stability of reactivity, Good matching and high catalytic efficiency
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Embodiment 1
[0018] Embodiment 1, embodiment 2, embodiment 3, embodiment 4, embodiment 5 are specific preparation methods of the bismuth silicate-containing catalytic material of the present invention.
Embodiment 6
[0019] Embodiment 6 and Embodiment 7 are application examples of the bismuth-containing silicate catalytic material of the present invention.
[0020] The comparative example is a synthesis method of the comparative catalytic material Ti-MCM-4l.
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[0021] Fig. 1 is gained pure powder bismuth silicate (Bi 2 SiO 5 ) powder X-ray diffraction pattern (XRD) of the sample.
[0022] When other non-amorphous carriers are used, the powder X-ray diffraction peaks of the carrier will be superimposed in the catalytic material, but the bismuth silicate (Bi 2 SiO 5 ) distribution and intensity of powder X-ray diffraction peaks.
[0023] Example 1
[0024] According to the molar ratio of silicon atoms in the silicon source to bismuth atoms in the bismuth source being 0.5:1, 1.0 mol of Bi(NO 3 ) 3 ·5H 2 O was dissolved in 5000mL of 1M sulfuric acid, and at 15°C, a mixture of 0.5mol ethyl silicate and 8.56mol ethanol was added to the abov...
Embodiment 2
[0026] According to the molar ratio of the silicon atoms in the silicon source to the bismuth atoms in the bismuth source is 5:2, 0.1mol of Bi 2 (SO 4 ) 3 Dissolve in 1300mL of 1M nitric acid, add a mixture of 0.5mol ethyl silicate and 4.28mol acetone at 15°C to the bismuth-containing nitric acid solution, and use 25% ammonia solution at 35°C Adjust the pH value to 8, stir for 10 hours, and then age at 52°C for 36 hours. The sample was taken out, washed and filtered several times, then dried and ground, and then roasted in the air at 540°C for 7 hours to obtain bismuth silicate (Bi 2 SiO 5 ) of the powdered catalytic material, which is numbered T-2, the test conditions of its XRD spectrum are the same as in Example 1, and the peak type and position of the crystal phase diagram diffraction peaks are similar to those in Fig. 1.
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