Normal-temperature dechlorinating agent for organochlorine and preparation method and application thereof
A technology of organic chlorine and dechlorination agent, which is applied in the direction of catalyst activation/preparation, separation methods, chemical instruments and methods, etc., can solve the problems of poor organic chlorine removal effect, achieve enhanced low-temperature adsorption capacity, increase chlorine capacity and dechlorination In addition to the effect of accuracy and time saving
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Embodiment 1
[0025] Step S1: Prepare 20 g of 0.5% sodium hydroxide solution with sodium hydroxide, weigh 3 g of pseudoboehmite, 8 g of sodium bentonite, and 12 g of lambsomite, dry mix the binder uniformly and add to the sodium hydroxide solution Carry out hydration in the medium to obtain a hydration binder;
[0026] Step S2: 110g of basic zinc carbonate, 10g of activated alumina powder, and 15g of sodium carbonate are mixed, then add a hydration binder, and after mixing uniformly, carry out granulation molding by an extruder or a ball rolling machine, and the molded granular catalyst Cured and matured in an incubator at a temperature of 50°C for 12 hours. The cured and matured catalyst was dried in an oven at a drying temperature of 110°C for 3 hours to obtain a dechlorination agent precursor;
[0027] Step S3: Put the dried catalyst in a muffle furnace for calcination at a temperature of 400° C. for 2 hours, and sieve to obtain a dechlorination catalyst.
Embodiment 2
[0029] Step S1: Sodium hydroxide is formulated into 20g of 0.5% sodium hydroxide solution, 2g of pseudoboehmite, 9g of sodium bentonite, 10g of sheepskin, and the binder is dry-mixed and added to the sodium hydroxide solution. 8 hours to obtain the hydration binder;
[0030] Step S2: 100g of basic zinc carbonate, 9g of activated alumina powder, and 15g of sodium bicarbonate are mixed, and then a hydration binder is added. The catalyst was maintained in an incubator at a temperature of 50°C for 12 hours. Dry the cured and matured catalyst in an oven at a drying temperature of 110°C for 3 hours to obtain a dechlorination agent precursor;
[0031] Step S3: Put the dried catalyst in a muffle furnace for calcination at a temperature of 400° C. for 2 hours, and sieve to obtain a dechlorination catalyst.
Embodiment 3
[0033] Step S1: Sodium hydroxide is formulated into 20 g of 1% sodium hydroxide solution, 2 g of pseudoboehmite, 9 g of sodium bentonite, and 10 g of sheepsweet are mixed evenly, and then added to the sodium hydroxide solution for hydration for 8 hours to obtain hydration binder;
[0034] Step S2: 90g of basic zinc carbonate, 8g of activated alumina powder, and 10g of sodium bicarbonate are mixed, then a hydration binder is added, after mixing evenly, granulation is carried out by an extruder or a rolling ball machine, and the formed granules The catalyst was maintained in an incubator at a temperature of 50°C for 8 hours. Dry the cured and matured catalyst in an oven at a drying temperature of 110°C for 3 hours to obtain a dechlorination agent precursor;
[0035] Step S3: Put the dried catalyst in a muffle furnace for calcination at a temperature of 400° C. for 2 hours, and sieve to obtain a dechlorination catalyst.
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