Preparation method of porous carbon loaded tungsten carbide composite material
A composite material and tungsten carbide technology, applied in the field of material science, can solve the problems of low hydrogen evolution catalytic activity and poor stability, and achieve the effects of short process flow, prevention of agglomeration and growth, and large specific surface area.
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Embodiment 1
[0028] Weigh 4.587g ammonium tungstate, 1.779g magnesium nitrate, 2.273g zinc nitrate, 1.968g calcium nitrate, 1.125g glycine and 1.72g glucose into a 500ml beaker, and add deionized water and stir to obtain a clear aqueous solution. The solution is heated on a resistance furnace, and a solution combustion synthesis reaction occurs, and a fluffy precursor can be obtained after the reaction. The precursor was placed in a tube furnace and fed with N 2 (The gas flow rate is 120mL / min) for high-temperature carbonization reaction, raising the temperature to 900°C at a rate of 6°C / min, and keeping it for 3 hours. After the reaction, a composite material of MgO / CaO / WC / C is obtained, and ZnO and carbon react and pyrolyze Pores are created on carbon substrates for the high-temperature evaporation of Zn simple substance. Immerse in the prepared 1.5M excess hydrochloric acid solution beaker, soak and let it stand for 30 hours, filter the supernatant, remove the lower layer of powder, wa...
Embodiment 2
[0030] Weigh 3.058g of ammonium metatungstate, 1.186g of magnesium nitrate, 1.515g of zinc nitrate, 1.312g of calcium nitrate, 0.65g of urea and 1.35g of glucose into a 300ml beaker, add deionized water and place it on a resistance furnace while heating slowly Stir to obtain a clear aqueous solution after stirring evenly, then put it into a muffle furnace and heat it at a constant temperature of 200°C for 1 hour to generate a solution combustion synthesis reaction. The powder is placed in a tube furnace under an Ar atmosphere (the gas flow rate is 150mL / min), and the heating rate is raised to 800°C at a rate of 7°C / min for carbonization for 4 hours to obtain a composite powder of MgO / CaO / WC / C, ZnO It reacts with carbon and pyrolyzes Zn simple substance to evaporate at high temperature to create pores on the carbon substrate. After re-grinding, immerse in the prepared 1.0M excess hydrochloric acid solution beaker, soak and let it stand for 48 hours, filter the supernatant, take...
Embodiment 3
[0032]Weigh 3.058g of ammonium metatungstate, 2.373g of magnesium nitrate, 1.92g of citric acid and 3.923g of sucrose into a 300ml beaker, add deionized water to obtain a clear aqueous solution, put the solution on a resistance furnace for heating, and In the solution combustion synthesis reaction, the solution is heated from the beginning until the gel is covered with a rubber stopper, and a fluffy precursor can be obtained after the reaction. Put the precursor into a tube furnace and feed it with Ar (the flow rate of the gas is 100mL / min) to carry out high-temperature carbonization reaction, raise the temperature to 1100°C for 2 hours at a rate of 10°C / min, and then cool with the furnace to obtain MgO Composite material of / WC / C. Immerse in the prepared 0.5M excess hydrochloric acid solution beaker, soak and let it stand for 40 hours, filter the supernatant, remove the lower layer of powder, wash with deionized water in a high-speed centrifuge for 4 times, and dry in a dryin...
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