A kind of transition metal phosphide hydrogenation catalyst and preparation method thereof
A technology of hydrogenation catalyst and transition metal, which is applied in the fields of denitrification catalyst and distillate oil hydrodesulfurization
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Embodiment 1
[0015] 10.9g of ammonium tungstate (8.4g in terms of WO), 47.1g of nickel nitrate (12.5g in terms of NiO) and 14.6g of ammonium dihydrogen phosphate (in terms of P 2 o 5 9.1 g in total) was dissolved in 54.3 g of deionized water to prepare solution A1. At room temperature, an equal volume of solution A1 was impregnated onto 70 g of the inorganic porous material, dried at room temperature for 12 hours, then dried at 110° C. for 8 hours, and calcined at 530° C. for 6 hours to obtain a transition metal phosphide hydrogenation catalyst precursor. The precursor was heated at room temperature at 30°C / h under N 2 Under the atmosphere, raise the temperature to 250°C, keep the temperature constant for 5 hours, switch to the hydrogen atmosphere, raise the temperature to 550°C at 30°C / h, and then reduce the temperature at constant temperature for 6 hours to obtain a transition metal phosphide hydrogenation catalyst, which is named Cat-A.
Embodiment 2
[0017] 12.9g of ammonium tungstate (9.9g in terms of WO), 41.9g of nickel nitrate (11.1g in terms of NiO) and 14.4g of ammonium dihydrogen phosphate (in terms of P 2 o 5 Total 9.0g) was dissolved in 54.3g deionized water to prepare solution A2. The following steps were the same as in Example 1 to obtain Cat-B.
Embodiment 3
[0019] 20.4g of ammonium tungstate (15.7g in terms of WO), 21.9g of nickel nitrate (5.8g in terms of NiO) and 13.7g of ammonium dihydrogen phosphate (in terms of P 2 o 5 8.5 g in total) was dissolved in 54.3 g of deionized water to prepare solution A3. The following steps were the same as in Example 1 to obtain Cat-C.
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