Method for preparing Ni2P by reducing nickel oxide precursor through thermal treatment at low temperature
A nickel oxide and precursor technology, applied in catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems such as difficulty in realizing temperature-programmed reduction, and achieve low equipment cost, short production cycle, Inexpensive effect
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Embodiment 1
[0014] First, 5.89 g of sodium hypophosphite (NaH 2 PO 2 .H 2 O) was added into 18mL deionized water, and after dissolving for 10min, 1.49g of NiO was added. After continuing to stir for 2 hours, the resulting solution was put into a petri dish and dried at 80°C. Then put the dried precursor powder into the reactor, heat treatment at 250°C for 10 minutes in a static nitrogen protection, and then wash the product with water and dry it. The obtained sample is named A, and A has an attached figure 1 Characteristics.
Embodiment 2
[0016] First, 5.93g of nickel nitrate (Ni(NO 3 ) 2 .6H 2 O) Added into 18mL deionized water, dissolved for 10min and then added 3.91g of MCM-41 molecular sieves. After continuing to stir for 2 hours, the resulting solution was put into a petri dish and dried at 100°C. Then put the dried precursor powder into a muffle furnace, and bake it in an air atmosphere at 550° C. for 2 hours to obtain supported nickel oxide (NiO / MCM-41). With stirring at room temperature, 5.89 g of NaH 2 PO 2 .H 2 O was added to 18 mL of deionized water, dissolved for 10 min and then added to the supported nickel oxide (NiO / MCM-41). After continuing to stir for 2 hours, the resulting solution was put into a petri dish and dried at 80°C. Then put the dried precursor powder into the reactor, heat treatment at 250°C for 10 minutes in a static nitrogen protection, and then wash the product with water and dry it. The obtained sample is named B, and B has an attached figure 2 Characteristics.
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