Metal nanowire network/mesoporous silica core-shell structure catalyst preparation method
A technology of mesoporous silica and core-shell structure, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve complex preparation steps and difficult large-scale Commercial synthesis and other issues, to achieve the effect of simple operation and improved stability
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Embodiment 1
[0040] Dissolve 145.78mg of cetyltrimethylammonium bromide in 10mL of chloroform, then add 10mL of 20mmol / L K 2 PtCl 4 Aqueous solution, stirring and reacting at 25°C for 2 hours, standing still, separating and removing the upper aqueous phase, then adding 90mL of deionized water, and adding 10mL of 300mmol / L NaBH at 1600 rpm 4 Aqueous solution, reacted for 5 minutes, finally added ammonia water to adjust the pH value to 10, and 144 μL tetraethyl orthosilicate, reacted for 1 hour at 35 ° C, transferred to a stainless steel reaction kettle with a polytetrafluoroethylene liner, in Crystallize at 100°C for 72 hours, wash, dry and calcinate to obtain a metal nanowire network / mesoporous silica core-shell structure catalyst.
[0041] The schematic diagram of this method is shown in figure 1 shown.
[0042] Such as figure 2 , compared with the sample without ethyl orthosilicate, the diameter of the wire mesh structure increased from 2nm to 3nm, indicating that a 0.5nm thick silico...
Embodiment 2
[0046] Embodiment 2: surfactant kind
[0047] Dissolve 115.35 mg of sodium cetyl sulfonate in 10 mL of chloroform, and then add 10 mL of 20 mmol / L K 2 PtCl 4 Aqueous solution, stirring and reacting at 25°C for 2 hours, standing still, separating and removing the upper aqueous phase, then adding 90mL of deionized water, and adding 10mL of 300mmol / L NaBH at 1600 rpm 4 Aqueous solution, reacted for 5 minutes, finally added ammonia water to adjust the pH value to 10, and 144 μL tetraethyl orthosilicate, reacted for 1 hour at 35 ° C, transferred to a stainless steel reaction kettle with a polytetrafluoroethylene liner, in Crystallize at 100°C for 72 hours, wash, dry and calcinate to obtain a metal nanowire network / mesoporous silica core-shell structure catalyst.
Embodiment 3
[0048] Embodiment 3: types of hydrophobic solvents
[0049] Dissolve 145.78mg of cetyltrimethylammonium bromide in 10mL of toluene, then add 10mL of 20mmol / L K 2 PtCl 4 Aqueous solution, stirring and reacting at 25°C for 2 hours, standing still, separating and removing the upper aqueous phase, then adding 90mL of deionized water, and adding 10mL of 300mmol / L NaBH at 1600 rpm 4 Aqueous solution, reacted for 5 minutes, finally added ammonia water to adjust the pH value to 10, and 144 μL tetraethyl orthosilicate, reacted for 1 hour at 35 ° C, transferred to a stainless steel reaction kettle with a polytetrafluoroethylene liner, in Crystallize at 100°C for 72 hours, wash, dry and calcinate to obtain a metal nanowire network / mesoporous silica core-shell structure catalyst.
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