Catalyst for preparing ethanol directly by acetic acid as well as preparation method and use thereof
A catalyst, acetic acid technology, applied in the field of catalytic chemistry, can solve the problems of high reaction temperature and reaction pressure, reduced commercial operability, harsh conditions, etc., to achieve the effect of reducing costs
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Embodiment A
[0048] Preparation of Pt 0.01%-Sn0.01% / SiO 2 Catalyst (no non-precious metal components, for comparison)
[0049] Mix the aqueous solution (0.67ml) of chloroplatinic acid (0.027g) and the dilute nitric acid solution (1ml) of tin oxalate (0.017g) and add water to form a 72.6ml impregnation solution, add it to 100g of silicon dioxide, and add it as you go. After stirring, the obtained material was dried in an oven gradually heated to 110° C. for 2 hours, and then calcined in a muffle furnace at 500° C. (heating rate, 2° C. / min) for 4 hours to obtain a catalyst sample.
Embodiment B
[0051] Preparation of Pt 0.09%-Sn0.09% / SiO 2 Catalyst (no non-precious metal components, for comparison)
[0052] Mix an aqueous solution (6.03ml) of chloroplatinic acid (0.243g) and a dilute nitric acid solution (1ml) of tin oxalate (0.153g) and add water to form a 72.6ml impregnating solution, which is added to 100g of silicon dioxide and added while adding After stirring, the obtained material was dried in an oven gradually heated to 120° C. for 3 hours, and then calcined in a muffle furnace at 500° C. (heating rate, 2° C. / min) for 4 hours to obtain a catalyst sample.
Embodiment C
[0054] Preparation of Pt 0.09%-Sn0.09%-Ni15% / SiO 2 Catalyst (catalyst according to the invention)
[0055] Mix an aqueous solution (6.03ml) of chloroplatinic acid (0.243g), a dilute nitric acid solution (1ml) of tin oxalate (0.153g) and an aqueous solution (50ml) of nickel nitrate (74.17g) and add water to form a 72.6ml impregnation solution , added to 100g of silicon dioxide, and stirred while adding, the obtained material was dried in an oven gradually heated to 110°C for 2 hours, and then roasted in a muffle furnace at 600°C (heating rate, 2°C / min) for 3 hours, the catalyst sample was obtained.
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