Catalyst for preparation of heptanol by hydrogenation of hyptyl aldehyde
A catalyst, a technology for producing heptanol, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, organic chemistry, etc., to achieve high activity and selectivity
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Embodiment 1
[0022] Embodiment 1. Weigh 0.5g of nickel nitrate hexahydrate and add 9ml of distilled water to dissolve and configure nickel nitrate solution, and impregnate the alumina carrier, and dry at 100°C to obtain a nickel-containing carrier; weigh 0.28g of potassium borohydride to make 12ml of aqueous solution , at room temperature the KBH 4 The solution is added dropwise to the nickel-containing carrier, the reaction proceeds immediately and hydrogen gas is released, after the dropwise completion, when no hydrogen gas is released, the catalyst is obtained by washing with deionized water until the solid product has no acid radicals.
Embodiment 2
[0023] Embodiment 2. Weigh 2.0 g of nickel nitrate hexahydrate and add 9 ml of distilled water to dissolve and configure it into a nickel nitrate solution, and impregnate it with a specific surface area of 150 m 2 g -1 Alumina carrier, dried at 100°C to obtain a nickel-containing carrier; weigh 1.11g of potassium borohydride to make 12ml of aqueous solution, and dissolve KBH at room temperature 4 The solution is added dropwise to the nickel-containing carrier, the reaction proceeds immediately and hydrogen gas is released, after the dropwise completion, when no hydrogen gas is released, the catalyst is obtained by washing with deionized water until the solid product has no acid radicals.
Embodiment 3
[0024] Example 3. Weigh 4.0 g of nickel nitrate hexahydrate and add 9 ml of distilled water to dissolve it to form a nickel nitrate solution, impregnate the alumina carrier, and dry at 100° C. to obtain a nickel-containing carrier; weigh 2.23 g of potassium borohydride to make 12 ml of aqueous solution , at room temperature the KBH 4 The solution is added dropwise to the nickel-containing carrier, the reaction proceeds immediately and hydrogen gas is released, after the dropwise completion, when no hydrogen gas is released, the catalyst is obtained by washing with deionized water until the solid product has no acid radicals.
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