The preparation method of glycine
A technology of glycine and catalyst, applied in the field of preparation of glycine, can solve the problems of toxic environmental impact of raw materials, consumption of metered acid and alkali, large environmental impact, etc., and achieves the effects of green and clean reaction route, promotion of oxidation reaction, and low cost of raw materials
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Embodiment 1
[0040] Dissolve 1 g of hydrated cobalt acetate in 100 ml of methanol, add 100 ml of methanol dissolved in 2 g of benzimidazole under stirring, continue to stir for 2 h, add 5 g of NaY molecular sieve, stir at 60 °C for 4 h, evaporate the solvent, and dry the obtained solid at 80 °C for 2 h Roast at 600 °C for 2 h under nitrogen protection to obtain nitrogen-doped carbon / NaY molecular sieve-supported cobalt catalyst (Co-N-C / NaY). Take 20 mg of the catalyst and add it to a 50 mL reaction kettle containing 2 g of ethanolamine and 8 g of deionized water, and stir. , heated to 100°C, filled with oxygen to a pressure of 1.0MPa, reacted for 8h, qualitatively and quantitatively analyzed the reaction product by gas chromatography-mass spectrometry, the conversion rate of ethanolamine was 99%, and the selectivity of glycine was 99%.
Embodiment 2-11
[0042] Examples 2-11 have studied the effect of different catalysts, and the specific procedures are similar to those of Example 1, except that different metal sources and different solid bases or metal oxide supports are used, and the catalysts are prepared at different temperatures. The calcination time is different, and other reaction conditions are the same as those in Example 1. The results are shown in Table 1.
Embodiment 2
[0043] The difference between embodiment 2 and embodiment 1 is: the metal source is 0.6g chloroauric acid; the solid base is 10g Mg(OH) 2 ; calcined at 500 °C for 3 h; finally, nitrogen-doped carbon / magnesium hydroxide supported gold catalyst (Au-N-C / Mg(OH) 2 ).
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