In situ synthesis of chiral modified palladium nanomaterials with different morphologies
A technology of in-situ synthesis and synthesis method, applied in nanotechnology, chemical instruments and methods, physical/chemical process catalysts, etc., to achieve the effect of broad application prospects
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Embodiment 1
[0024] Example 1: Add 400 mg of proline to 100 mL of deionized water, stir and dissolve at 50 °C under normal pressure nitrogen atmosphere, add 800 uL of 0.1 M ascorbic acid after 20 minutes, stir evenly, and add 5 mL of 10 mM chloropalladic acid , and the reaction was stirred for 30 min. After the reaction, the product was collected by centrifugation. The sample was washed twice with water and twice with ethanol. The obtained product was dispersed in ethanol, and the product characterization results were as follows: Figure 1-2 .
Embodiment 2
[0025] Example 2: Add 75 mg of tartaric acid to 100 mL of deionized water, stir and dissolve at 40 °C under normal pressure nitrogen atmosphere, add 5 mL of 10 mM chloropalladic acid after 20 min, stir for 5 min, and add 1 mL of 0.1 M ascorbic acid, The reaction was stirred for 60 min. After the reaction, the product was collected by centrifugation. The sample was washed twice with water and twice with ethanol. The obtained product was dispersed in ethanol, and the product characterization results were as follows: image 3 .
Embodiment 3
[0026] Example 3: Add 75 mg of tartaric acid to 100 mL of deionized water, stir and dissolve at 90 °C under normal pressure nitrogen atmosphere, add 5 mL of 10 mM chloropalladic acid after 20 min, stir for 5 min, and add 1 mL of 0.1 M ascorbic acid, The reaction was stirred for 60 min. After the reaction, the product was collected by centrifugation. The sample was washed twice with water and twice with ethanol. The obtained product was dispersed in ethanol, and the product characterization results were as follows: Figure 4 .
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