Magnetic titanium silicon molecular sieve with compact protective layer and its application
A technology of titanium-silicon molecular sieve and protective layer, which is applied in the application field of the reaction of propylene chloride epoxidation to epichlorohydrin, can solve the problems of equipment corrosion, many by-products, long process flow, etc., and achieve no corrosion of equipment, No pollution equipment, high catalytic activity effect
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Embodiment 1
[0038] 200ml, 2.0×10 -2 M FeCl 3 Add it into a 250ml three-neck flask, and reflux at 100°C for 2 days. The reaction product is centrifuged, washed with deionized water, and dried at room temperature to obtain Fe nanoparticles.
[0039] Take 0.5g Fe nanoparticles and add to 50ml containing 0.45M NH 3 ·H 2 O, 3.05M H 2 O in isopropanol solution, stirred at 40°C for 30min, then quickly added 100ml, 4.0×10 -3 Tetraethyl silicate (TEOS) of M was treated at room temperature for 15 h, the particles were collected by centrifugation, washed with ethanol, dried at 60 °C, and calcined at 800 °C for 5 h under Ar atmosphere to obtain dense SiO 2 layer of Fe / SiO 2 magnetic core.
[0040] Take 1g Fe / SiO 2 powder, and 40mL of 2mol / L glucose solution were added to a 50mL stainless steel reaction kettle, and crystallized at 180°C for 24h to obtain Fe / SiO with a C layer on the surface 2 nanomaterials.
[0041] Take a certain amount of butyl titanate (TBOT) and add it to tetraethyl orth...
Embodiment 2
[0044] The preparation method of catalyst is the same as embodiment 1. SiO of titanium silicon mother liquor 2 :TiO 2 =1:0.01, the analytical method of reaction conditions and product is the same as embodiment 1. The results of catalyst activity are as follows: the conversion rate of allyl chloride is 68.6%, and the selectivity to epichlorohydrin is 88.1%.
Embodiment 3
[0046] The preparation method of catalyst is the same as embodiment 1. SiO of titanium silicon mother liquor 2 :TiO 2 =1:0.04, the analytical method of reaction conditions and product is the same as embodiment 1. The results of catalyst activity are as follows: the conversion rate of allyl chloride is 77.3%, and the selectivity to epichlorohydrin is 93.2%.
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