Method for reclaiming precious metal from metallic carrier catalyst device
A catalyst device and metal carrier technology, applied in metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, catalyst activation/preparation, etc., can solve problems such as difficult selective separation of catalyst layers
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reference example 1
[0027] Coat 140g of activated alumina on a heat-resistant stainless steel honeycomb body with a diameter of 900mm and a height of 1260mm (hereinafter referred to as a metal carrier; a capacity of 800cc). After sintering, 0.3g of platinum (Pt), 2.3g of Palladium (Pd) and 0.3g rhodium (Rh) are used to make a metal supported catalyst device.
Embodiment 1
[0029] According to the flow chart shown in FIG. 1, the metal supported catalyst device prepared in Reference Example 1 was immersed in an aqueous solution containing 20% by weight of sulfuric acid and 2% by weight of nitric acid, and treated at 80° C. for 5 hours. After standing to cool, the metal carrier (1) was taken out from the aqueous solution, the metal carrier was washed with water, and the washing solution was mixed with the aqueous solution to obtain an aqueous solution (2) containing undissolved residues. The recovered metal support was identical in appearance to the metal support before being coated with activated alumina, without any trace of dissolution.
[0030] Filter the aqueous solution (2), after separating the undissolved residue (3) from the aqueous solution (4), add 10 g of iron (Fe) powder in the aqueous solution (4) and carry out reduction treatment, so that the noble metal (Pt, Pd, Rh) components (5 ) precipitation and recovery. Next, the recovered ...
Embodiment 2
[0032] According to the flow chart shown in Fig. 1, the metal carrier catalyst device that will make in reference example 1 is immersed in the aqueous solution that contains 20% by weight sulfuric acid and 2% by weight nitric acid, handles 5 hours at 80 ℃, metal carrier (1 ) was taken out from the above aqueous solution, then dipped into a newly prepared aqueous solution containing 20% by weight of sulfuric acid and 2% by weight of nitric acid, and then treated at 80° C. for 5 hours. After standing to cool, the metal support was washed with water, and the washing solution was mixed with the aqueous solution to obtain an aqueous solution (2) containing undissolved residue. The recovered metal support was identical in appearance to the metal support before being coated with activated alumina, without any trace of dissolution.
[0033] Filter the aqueous solution (2), after separating the undissolved residue (3) from the aqueous solution (4), add 10 g of iron (Fe) powder in the...
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