A method for separating palladium from acidic aqueous solution
The technology of an acidic aqueous solution and an aqueous nitric acid solution is applied in the field of separation of palladium, which can solve the problems such as lack of separation means, and achieve the effects of high separation efficiency, simple operation and high selectivity.
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Embodiment 1
[0026] Dissolve 0.5g of the compound bis(2,4,4-trimethylpentyl)dithiophosphinic acid shown in structural formula I in 45.0mL of dichloromethane, mix well to obtain a solution; add 4.5 gSiO 2 -P Stir evenly, and use a rotary evaporator to evaporate dichloromethane under reduced pressure to volatilize the methylene chloride until the material is in a near-dry state, and then vacuum-dry the near-dry material at 55°C for 24 hours to obtain an adsorbent.
Embodiment 2
[0028] Dissolve 0.5g of the compound bis(2,4,4-trimethylpentyl)dithiophosphinic acid shown in structural formula I in 40.0mL of dichloromethane, mix well to obtain a solution; add 4.0 gSiO 2 -P Stir evenly, and use a rotary evaporator to evaporate dichloromethane under reduced pressure to volatilize the material to a near-dry state, and then vacuum-dry the near-dry material at 50°C for 24 hours to obtain an adsorbent.
Embodiment 3
[0030] Dissolve 0.5g of the compound bis(2,4,4-trimethylpentyl)dithiophosphinic acid shown in structural formula I in 50.0mL of dichloromethane, mix well to obtain a solution; add 5.5 gSiO 2 -P Stir evenly, and use a rotary evaporator to evaporate dichloromethane under reduced pressure to volatilize the methylene chloride until the material is in a near-dry state, and then vacuum-dry the near-dry material at 60°C for 24 hours to obtain an adsorbent.
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