Nickel hydrogenation catalyst with large pore volume and high sulfur resistance
A hydrogenation catalyst and catalyst technology, applied in the field of catalysis, can solve problems such as low catalytic activity, poor resistance to impurities, and influence on catalyst activity
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Embodiment 1
[0020] Configure nickel chloride solution A, where Ni 2+ The ion concentration is 1mol / L respectively. 19.01g copper nitrate trihydrate (Cu(NO 3 ) 2 ·3H 2 O), 14.47g ferric nitrate trihydrate (FeN 3 o 9 9H 2 O), 0.31g lanthanum nitrate (LaN 3 o 9 ·6H 2 O) Add deionized water to dissolve and configure solution B. The carrier silica is added to solution B and stirred vigorously to obtain a slurry containing insoluble compounds, and then the slurry is spray-dried by air flow to obtain a catalyst precursor. Then impregnate the catalyst precursor with nickel chloride solution A, 120 o C drying, repeated several times, until the solid powder with the required nickel load is achieved. 500 o C was calcined for 10 h to obtain the finished catalyst. The physical properties of the resulting catalysts are listed in Table 1.
Embodiment 2
[0022] Prepare catalyst according to embodiment 1, but use 116.88g zinc acetate dihydrate (C 4 h 6 o 4 Zn.2H 2 O), 36.17g ferric nitrate trihydrate (FeN 3 o 9 9H 2 O), 0.31g cerium nitrate hexahydrate (CeN 3 o 9 ·6H 2 O) Add deionized water to dissolve and configure solution B. The physical properties of the resulting catalysts are listed in Table 1.
Embodiment 3
[0024] Prepare catalyst according to embodiment 1, but use 38.02g copper nitrate trihydrate (Cu(NO 3 ) 2 ·3H 2 O), 9.14g manganese nitrate tetrahydrate (MnN 2 o 6 4H 2 O), 0.31g cerium nitrate hexahydrate (CeN 3 o 9 ·6H 2 O) Add deionized water to dissolve and configure solution B. The physical properties of the resulting catalysts are listed in Table 1.
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