Graphene composite photocatalytic glass fiber electrode material and preparation method thereof
A graphene composite and photocatalytic material technology, which is applied in the field of graphene composite photocatalytic glass fiber electrode materials and its preparation, can solve the problems of low charge efficiency, unfavorable electrode material preparation, and increased production costs.
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Embodiment 1
[0040]Weigh 4 g of glucose and 2 g of nano-zinc oxide, dissolve them in 50 ml of deionized water, and ultrasonically disperse for 30 min. Take 40 parts of ultra-fine glass fiber cotton with a diameter of 3.0 μm and 10 parts of ultra-fine glass fiber cotton with a diameter of 1.0 μm, and break the glass fiber cotton at a speed of 6000 rpm for 3 minutes through a fiber dissociator. A pulp suspension with a mass concentration of 6 wt% was prepared. It is transported by the slurry conveyor to the forming paper machine for wet forming and then made into sheets. Put the flakes of ultra-fine glass fiber into 50 mL of 3 mol / L hydrochloric acid solution for 30 min, and at the same time dry it on a drying plate at 100 °C for 5 min. Then pickling and drying the glass fiber. The above-prepared filter paper was placed in a microwave fast reactor at 100 °C for 6 min. The glass fiber CDI electrode material of the graphene composite photocatalytic material synthesized in situ was soaked in...
Embodiment 2
[0042] Weigh 6 g of glucose and 2 g of nano-zinc oxide, dissolve them in 50 ml of deionized water, and ultrasonically disperse for 30 min. Take 40 parts of ultrafine glass fiber cotton with a diameter of 3.5 μm and 10 parts of ultrafine glass fiber cotton with a diameter of 1.5 μm, and break the glass fiber cotton at a speed of 7000 rpm for 4 minutes through a fiber dissociator. A pulp suspension with a mass concentration of 7 wt% was prepared. It is transported by the slurry conveyor to the forming paper machine for wet forming and then made into sheets. Put the flakes of ultra-fine glass fiber into 50 mL of 4.5 mol / L hydrochloric acid solution for 45 min, and dry it on a drying plate at 100 °C for 5 min at the same time, and then pickle the dried glass fiber. The filter paper prepared above was placed in a microwave fast reactor at 150 °C for 8 min. The glass fiber electrode material of in-situ synthesized graphene composite photocatalytic particle material was soaked in t...
Embodiment 3
[0044] Weigh 8 g of glucose and 3 g of nano-titanium oxide, dissolve them in 50 ml of deionized water, and ultrasonically disperse for 30 min. Take 40 parts of ultra-fine glass fiber cotton with a diameter of 3.5 μm and 10 parts of ultra-fine glass fiber cotton with a diameter of 1.5 μm, and break the glass fiber cotton through a fiber dissociator at a speed of 8000 rpm for 4 minutes. A pulp suspension with a mass concentration of 9 wt% was prepared. It is transported by the slurry conveyor to the forming paper machine for wet forming and then made into sheets. Put the flakes of ultra-fine glass fiber into 50 mL of 6 mol / L hydrochloric acid solution for 60 min, and dry it on a drying plate at 100 °C for 6 min at the same time, put the filter paper prepared above into a microwave fast reactor at 200 °C, React for 12 min. The in-situ synthesized graphene composite photocatalytic material glass fiber electrode material was soaked in the binder system mixed with polyurethane mod...
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