Biological reducing preparation method of catalyst used for synthesizing pyruvaldehyde
A catalyst, glyoxal technology, applied in catalyst activation/preparation, microorganism-based methods, biochemical equipment and methods, etc., can solve the problem of high reaction temperature requirements, easy carbon deposition on the catalyst surface, and increased reaction bed pressure, etc. problems, to achieve the effect of good activity and selectivity, small catalyst dosage, and easy recycling
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Embodiment 1
[0020] Preparation of bacterial suspension: Weigh 1.0g of finely ground dry Pichia pastoris powder, add 80mL of deionized water, stir and oscillate evenly for later use; preparation of silver ammonia solution: weigh 15.74g of silver nitrate, add deionized water to dissolve, Add 10% ammonia solution dropwise until the precipitate just disappears, and make up to 100 mL with deionized water; prepare 2 mol / L NaOH solution.
[0021] In a 500mL Erlenmeyer flask, mix 80mL of bacterial suspension, 10mL of silver ammonia solution, and 10mL of NaOH solution evenly, then the concentration of bacterial powder in the reaction system is 10g / L, the concentration of silver is 10g / L, and the concentration of NaOH solution is 0.2mol / L . The mixed solution was placed in a water-bath shaker (120r / min) at 60°C for oscillating reaction for 8h; after the reaction, the mixed solution was centrifuged (3000r / min), and the clear solution obtained a stable silver sol containing a certain amount of biomas...
Embodiment 2
[0026] Take 0.4482g of the lower layer of silver powder in Example 1 and dissolve it in 1.334mL of deionized water. Add 2 g of ZrO to the above solution 2 , stirred evenly, impregnated at room temperature for 16 hours, dried at 110°C for 2 hours, and then calcined at 450°C for 1 hour to obtain catalyst A2, whose composition is shown in Table 1. Catalyst evaluation is the same as in Example 1, and the results are shown in Table 1.
Embodiment 3
[0028] Take 0.2976 g of the upper layer silver powder described in Example 1 and dissolve it in 2.83 mL of deionized water. Add 2 g of α-Al to the above solution 2 o 3 , stirred evenly, impregnated at room temperature for 16 hours, dried at 110°C for 2 hours, and then calcined at 450°C for 1 hour to obtain catalyst A3, whose composition is shown in Table 1. Catalyst evaluation is the same as in Example 1, and the results are shown in Table 1.
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