Tin-titanium-silicon molecular sieve, preparation method and application thereof, and sulfide oxidation method
A technology of tin-titanium-silicon molecular sieve and titanium-silicon molecular sieve is applied in the field of sulfide oxidation, which can solve the problems of occupying land resources and inventory space, and achieve the effects of modulation selectivity and good catalytic effect.
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[0028] According to a preferred embodiment of the present invention, the molecular sieve satisfies nSn / nTi=A, I 960 / I 800 =B, B=i(A+1)nTi, wherein 0.1960 Infrared absorption spectrum of molecular sieve at 960cm -1 Absorption intensity in the vicinity, I 800 Infrared absorption spectrum of molecular sieve at 800cm -1 Absorption strength in the vicinity. Preferably, 0.2<A<3, 0.3<B<0.7. In this way, it can be more conducive to the diffusion of reactants and product molecules in the catalytic oxidation reaction, not only can further improve the conversion rate of thioether, but also can more effectively adjust the selectivity of the target product. For example, when used in the oxidation reaction of thioether, the conversion rate of thioether can be further improved, and the selectivity of the target product sulfone can be more effectively adjusted.
[0029] According to the molecular sieve of the present invention, preferably the molecular sieve satisfies T w / T k =D, 0.2...
Embodiment 1
[0119] This example illustrates the methods and products provided by the invention.
[0120] At normal temperature (20°C, the rest of the comparative examples are the same as the examples) and normal pressure (0.1MPa, the rest of the comparative examples are the same as the examples), the deactivated cyclohexanone oximation catalyst SH-2 and 1mol / L hydrochloric acid The aqueous solution was mixed and beaten, and then the mixed slurry was mixed and stirred at 80°C for 12 hours; after solid-liquid separation, the solid, tin source tin chloride pentahydrate, organosilicon source tetraethyl orthosilicate, and sodium hydroxide aqueous solution (pH 12 ) mixed, and after tetraethyl orthosilicate was hydrolyzed (the hydrolysis rate of the organic silicon source was 40%), the mixture was transferred to a stainless steel sealed reaction kettle, treated at 100°C for 10h, and then at 170°C for 12h, wherein, inactivation Cyclohexanone oximation catalyst: tin source: organosilicon source: a...
Embodiment 2
[0122] This example illustrates the methods and products provided by the invention.
[0123] At normal temperature and pressure, first mix the deactivated cyclohexanone oximation catalyst SH-3 with 5mol / L hydrochloric acid solution for beating, then mix and stir the mixed slurry at 60°C for 1 hour; after solid-liquid separation, separate the solid, Tin source tin chloride pentahydrate, organosilicon source methyl orthosilicate and tetrapropyl ammonium hydroxide aqueous solution (pH is 10) are mixed, treat that orthosilicate methyl ester is hydrolyzed (organosilicon source hydrolysis rate is 50%) The mixture was transferred to a stainless steel sealed reactor, treated at 130°C for 4h, and then at 150°C for 20h, wherein the molar ratio of deactivated cyclohexanone oximation catalyst: tin source: organosilicon source: acid: alkali: water 100:2:1:15:15:200, deactivated cyclohexanone oximation catalyst and organosilicon source with SiO 2 In terms of acid, H + In terms of base, in...
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