Preparation method of chloroauric acid
A chloroauric acid and hydrochloric acid technology, applied in the field of chloroauric acid, can solve the problems of polluting the environment, toxic red nitrogen oxide gas, and affecting the purity of the final product, so as to avoid pollution and ensure the purity of the product
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Embodiment 1
[0022] Put the gold powder in a multi-mouth beaker, heat it to 80°C in a methyl silicone oil bath, add one-fifth of hydrochloric acid, and start stirring. Use a separatory funnel to add dropwise mass fraction of 15wt% hydrogen peroxide (amount of 2.25, taking the gold powder as 1) and remaining hydrochloric acid. The amount of hydrochloric acid is 6 substances, and the gold powder is 1. The mass fraction is 37wt% hydrochloric acid. React 25min to end the reaction.
[0023] After reacting to the complete dissolution of the gold powder, start to evaporate the solution until the red and black sticky pepper (this time the volume of the solution is about the size of the original volume), stop evaporating, cool with cold water and stir, and the orange-yellow chloroauric acid crystals are separated out immediately, and the obtained sample is washed with concentrated sulfuric acid. After drying, store in a desiccator filled with silica gel. This example collects the yield of chloroa...
Embodiment 2
[0025] Put the gold powder in a multi-mouth beaker, heat it to 100°C in a methyl silicone oil bath, add one-fifth of hydrochloric acid, and start stirring. Use a separatory funnel to add dropwise mass fraction of 35wt% hydrogen peroxide (amount of 2.25, based on the amount of gold powder as 1) and remaining hydrochloric acid. The amount of hydrochloric acid is 10 wt. The mass fraction is 30wt% hydrochloric acid. React 5min to end the reaction.
[0026] After reacting to the complete dissolution of the gold powder, start to evaporate the solution until the red and black sticky pepper (this time the volume of the solution is about the size of the original volume), stop evaporating, cool with cold water and stir, and the orange-yellow chloroauric acid crystals are separated out immediately, and the obtained sample is washed with concentrated sulfuric acid. After drying, store in a desiccator filled with silica gel. This example collects the yield of chloroauric acid to be 98.7%...
Embodiment 3
[0028] Put the gold powder in a multi-mouth beaker, heat it to 100°C in a methyl silicone oil bath, add one-fifth of hydrochloric acid, and start stirring. Use a separating funnel to add dropwise mass fraction of 35wt% hydrogen peroxide (amount of 7.5, based on the amount of gold powder as 1) and remaining hydrochloric acid. The amount of hydrochloric acid is 10 wt. The mass fraction is 37wt% hydrochloric acid. React 5min to end the reaction.
[0029] After reacting to the complete dissolution of the gold powder, start to evaporate the solution until the red and black sticky pepper (this time the volume of the solution is about the size of the original volume), stop evaporating, cool with cold water and stir, and the orange-yellow chloroauric acid crystals are separated out immediately, and the obtained sample is washed with concentrated sulfuric acid. After drying, store in a desiccator filled with silica gel. This example collects the yield of chloroauric acid to be 99.6%,...
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