Compound catalyst with nanometer core-shell structure and preparing method of compound catalyst
A composite catalyst and nano-core-shell technology, applied in catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems such as weak interaction force, low catalytic performance, uncontrollable catalyst structure, etc., to achieve Effects of preventing agglomeration, improving catalytic performance, and being easy to control
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[0038] The present invention also provides the preparation method of the composite catalyst of above-mentioned nano core-shell structure, and its preparation process is as follows figure 2 As shown, it mainly includes the following steps:
[0039] Step 1, mix the metal oxide precursor and the alkaline substance at a mass ratio of 1:1-5 to make a solution, react at 100-200°C for 12-48h, and then cool to room temperature, at 3000-10000rpm Centrifuge the solution at a rotating speed for 5-10min to obtain a solid product A; wherein the metal oxide precursor is Al 2 o 3 , Ga 2 o 3 , SiO 2 、GeO 2 、TiO 2 , ZrO 2 , V 2 o 5 、Cr 2 o 3 , MnO 2 , Fe 2 o 3 , Fe 3 o 4 、Co 2 o 3 , NiO, CuO, ZnO, Nb 2 o 5 、MoO 3 , RuO 2 、In 2 o 3 , CeO 2 , Sb 2 o 3 , Sb 2 o 5 , Tl 2 o 3 , PbO, Bi 2 o 3 , La 2 o 3 、 Ta 2 o 5 、WO 2 、WO 3 or SnO 2 One or more of nitrates, phosphates, sulfates, sulfites, chlorates or carbonates; the alkaline substances are NaOH, KOH, Ba(OH...
Embodiment 1
[0047] Use PbO, its precursor is nitrate, the noble metal is Pb, its precursor is Pb nitrate, the alkaline solution can be NaOH, and the carbon source can be glucose, fructose, sucrose or sucrose. Concrete preparation process is as follows;
[0048] Step 1, mix the precursor nitrate of PbO with NaOH according to the mass ratio of 1:5 and make a solution, react at 100°C for 24h, then cool to room temperature, and then centrifuge the solution at 3000rpm for 5min , to obtain solid product A;
[0049] In step 2, the solid product A is centrifuged and washed with ethanol and deionized water, and then freeze-dried in a vacuum environment for 5 hours to obtain PbO nanoparticles, and the particle size of the PbO nanoparticles is 20-50nm.
[0050] Step 3, dissolve 10g of PbO nanoparticles in deionized water, add 200g of surfactant, then add 500g of carbon source, the carbon source is glucose, after stirring for 2h, react the mixed solution at 150°C for 3h, then cool to At room temper...
Embodiment 2
[0055] The metal oxide used in this example is Al 2 o 3 , Ga 2 o 3 , SiO 2 、GeO 2 、TiO 2 , ZrO 2 , V 2 o 5 、Cr 2 o 3 , MnO 2 , Fe 2 o 3 , Fe 3 o 4 、Co 2 o 3 , NiO, CuO, ZnO, Nb 2 o 5 、MoO 3 , RuO 2 、In 2 o 3 , CeO 2 , Sb 2 o 3 , Sb 2 o 5 , Tl 2 o 3 、 Bi 2 o 3 , La 2 o 3 、 Ta 2 o 5 、WO 2 、WO 3 、 Bi 2 o 3 and SnO 2 A kind of in; Its implementation process is all identical with embodiment 1, obtains corresponding metal oxide nanoparticle at last, and is covered with carbon layer on it, is covered with a plurality of Pb nanoparticles on the carbon layer, the particle diameter of Pb nanoparticle Between 2-10nm.
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