Method for preparing high-yield hydrothermal carbon microspheres through slurrying pre-hydrolysis liquid
A technology of pre-hydrolyzate and carbon microspheres, which is applied in chemical instruments and methods, adsorption water/sewage treatment, alkali metal oxides/hydroxides, etc., can solve the problems of high price and difficult separation and purification of pre-hydrolyzate, Achieve the effects of simple operation, value-added utilization and high yield
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Embodiment 1
[0020] (1) Add 1.6 g of sulfuric acid (calculated without water) to the 20 g pulping pre-hydrolyzate to make the acid concentration of the pre-hydrolyzate reach 8%;
[0021] (2) Add 0.12 g of acrylic acid as a functional agent to the pulping pre-hydrolyzate obtained in step (1), place the solution in a 40 mL polytetrafluoroethylene reactor, and conduct a hydrothermal reaction at 180°C for 12 hours, and wait for the device to cool , the solid-liquid separation of the obtained mixture was carried out by vacuum filtration, and the solid was washed with ethanol and water several times, and then dried in a vacuum oven at 60°C to obtain high-yield hydrothermal carbon microspheres;
[0022] (3) Disperse the above-mentioned hydrothermal carbon microspheres in a sodium hydroxide solution, stir and activate them for 1 hour, filter them, and wash the carbon microspheres with deionized water until they are neutral to obtain a high-yield functionalized hydrothermal carbon Microspheres.
Embodiment 2
[0024] (1) Add 1 g of hydrochloric acid (calculated without water) to 20 g of pulping pre-hydrolyzate to make the acid concentration of the pre-hydrolyzate reach 5%;
[0025] (2) Add 0.1 g of acrylic acid as a functional agent to the pulping pre-hydrolyzate obtained in step (1), place the solution in a 40 mL polytetrafluoroethylene reactor, and conduct a hydrothermal reaction at 160°C for 14 hours, and wait for the device to cool down , the solid-liquid separation of the obtained mixture was carried out by vacuum filtration, and the solid was washed with ethanol and water several times, and then dried in a vacuum oven at 60°C to obtain high-yield hydrothermal carbon microspheres;
[0026] (3) Disperse the above-mentioned hydrothermal carbon microspheres in sodium hydroxide solution, stir and activate them for 2 hours, filter them, and wash the carbon microspheres with deionized water to neutrality, that is, a high-yield functionalized hydrothermal carbon Microspheres.
Embodiment 3
[0028] (1) Add 0.4 g of nitric acid (calculated without water) to 20 g of pulping pre-hydrolyzate to make the acid concentration of pre-hydrolyzate to 2%;
[0029] (2) Add 0.15 g of acrylic acid as a functional agent to the pulping pre-hydrolyzate obtained in step (1), place the solution in a 40 mL polytetrafluoroethylene reactor, and conduct a hydrothermal reaction at 190°C for 8 hours, and wait for the device to cool down , the solid-liquid separation of the obtained mixture was carried out by vacuum filtration, and the solid was washed with ethanol and water several times, and then dried in a vacuum oven at 60°C to obtain high-yield hydrothermal carbon microspheres;
[0030] (3) Disperse the above-mentioned hydrothermal carbon microspheres in potassium hydroxide solution, stir and activate them for 3 hours, filter them, and wash the carbon microspheres with deionized water to neutrality, that is, a high-yield functionalized hydrothermal carbon Microspheres.
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