Sodium borohydride hydrolysis hydrogen production catalyst, preparation method and application thereof
A hydrogen production technology of sodium borohydride and hydrolysis, applied in organic compound/hydride/coordination complex catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve problems such as shedding, and achieve low cost and high conditions Gentle, high-yield results
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Embodiment 1
[0040] Preparation of NiCoP / RC-malic acid catalyst
[0041] First, 20 g of phosphoramidate chelating resin was ball-milled for 3 hours to make it into powder. Subsequently, nickel chloride and cobalt chloride were dissolved in ultrapure water to prepare 0.15mol. L -1 250mL of nickel chloride solution and 250mL of cobalt chloride solution were mixed together to form solution A; the ball-milled aminophosphoric acid chelating resin was added to solution A, and stirred at a speed of 750r / min for 24h; The resulting solution was then suction-filtered under reduced pressure and washed with distilled water. Afterwards, the obtained solid was vacuum-dried at 50°C for 6h; and calcined in a tube furnace at 1000°C for 1h, under nitrogen protection during the calcination process, and the heating rate was 5°C / min to obtain NiCoP / RC.
[0042] The NiCoP / RC prepared above was mixed with malic acid at a mass ratio of 1:1 and ball milled for 3 hours to obtain a NiCoP / RC-malic acid mixed catal...
Embodiment 2
[0049] Preparation of NiP / RC-citric acid catalyst
[0050] First, 20 g of phosphoramidate chelating resin was ball-milled for 3 hours to make it into powder. Subsequently, nickel chloride was dissolved in ultrapure water to prepare 0.05mol L -1 The solution. Secondly, the aminophosphoric acid chelating resin after ball milling is added in the 250mL nickel chloride solution, and stirs 24h with the speed of 750r / min. The resulting solution was then vacuum filtered and washed with distilled water. Afterwards, the obtained solid was vacuum-dried at 50° C. for 6 h. And calcined in a tube furnace at 600°C for 5h, under nitrogen protection during the calcining process, with a heating rate of 5°C / min, to obtain NiP / RC.
[0051] The NiP / RC prepared above was mixed with citric acid at a mass ratio of 1:0.5 and ball milled for 3 hours to obtain a NiP / RC-citric acid mixed catalyst.
[0052] Subsequently, with 1g of sodium borohydride, 0.2g of prepared catalyst is ground and mixed uni...
Embodiment 3
[0055] Preparation of CoP / RC-phosphoric acid catalyst
[0056] First, 20 g of phosphoramidate chelating resin was ball-milled for 3 hours to make it into powder. Subsequently, cobalt nitrate was dissolved in ultrapure water to prepare 2.5mol L -1 The solution. Secondly, the aminophosphoric acid chelating resin after ball milling is added in the 500mL cobalt nitrate solution, and stirs 24h with the speed of 750r / min. The resulting solution was then vacuum filtered and washed with distilled water. Afterwards, the obtained solid was vacuum-dried at 50° C. for 6 h. And calcined in a tube furnace at 1100°C for 3h, under the protection of nitrogen during the calcining process, and the heating rate was 10°C / min to obtain CoP / RC.
[0057] The CoP / RC prepared above was mixed with oxalic acid at a mass ratio of 1:10 and ball milled for 3 hours to obtain a CoP / RC-oxalic acid mixed catalyst.
[0058] Subsequently, with 1g of sodium borohydride, 0.2g of prepared catalyst is ground and...
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