Preparation method and application of a noble metal-doped Wo3-based formaldehyde gas-sensitive material
A precious metal, formaldehyde gas technology, applied in the direction of material electrochemical variables, tungsten oxide/tungsten hydroxide, etc., can solve the problems of slow response and recovery speed, poor selectivity of formaldehyde gas sensor, etc., to promote the conversion rate and speed up the response and recovery speed. , improve the effect of the reaction
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Embodiment 1
[0028] Weigh 6.6g of sodium tungstate and dissolve in 100ml of deionized water, stir magnetically for 30min to form a uniform solution, then add 3mol / L hydrochloric acid dropwise to adjust the pH of the solution to 1, and continue stirring for 30min to form a light yellow liquid. Then add 30ml of 0.17mol / L CTAB solution, stir evenly and transfer to a reaction kettle with a 200ml polytetrafluoroethylene liner to make the volume filling rate 75%. The reaction kettle was kept in an oven at 180°C for 24 hours and then cooled to room temperature. After washing with water and alcohol three times, the precipitated product was dried in an oven at 60°C for 12 hours. After drying, the product was sintered in a muffle furnace at 450 °C for 2 h. Such as figure 1 The electron microscope image shown.
[0029] Get 2g of samples and ultrasonically disperse them in 20ml of absolute ethanol, add dropwise a chloroplatinic acid solution with a concentration of 0.039mol / L according to the molar ...
Embodiment 2
[0033]Weigh 1.65g of sodium tungstate and dissolve in 100ml of deionized water, stir magnetically for 30min to form a uniform solution, then add 3mol / L hydrochloric acid dropwise to adjust the pH of the solution to 1, and continue stirring for 30min to form a light yellow liquid. Then add 30ml of 0.042mol / L CTAB solution, stir evenly and transfer to a reaction kettle with 200ml polytetrafluoroethylene liner to make the volume filling rate 75%. The reaction kettle was kept in an oven at 120°C for 16 hours and then cooled to room temperature. The precipitated product was washed with water and alcohol three times, and then dried in an oven at 60°C for 12 hours. After drying, the product was sintered in a muffle furnace at 550 °C for 2 h.
[0034] Get 2g of sample and ultrasonically disperse it in 20ml of absolute ethanol, add dropwise a chloroplatinic acid solution with a concentration of 0.039mol / L according to the molar ratio Pt:W of 1%, adjust its pH value to 9 with ammonia wa...
Embodiment 3
[0036] Weigh 16.5g of sodium tungstate and dissolve in 100ml of deionized water, stir magnetically for 30min to form a uniform solution, then add 2mol / L hydrochloric acid dropwise to adjust the pH of the solution to 0.5, and continue stirring for 30min to form a light yellow liquid. Then add 30ml of 0.42mol / L CTAB solution, stir evenly and transfer to the reaction kettle with 200ml polytetrafluoroethylene liner to make the volume filling rate 75%. The reaction kettle was kept in an oven at 200°C for 18 hours and then cooled to room temperature. After washing with water and alcohol three times, the precipitated product was dried in an oven at 60°C for 12 hours. After drying, the product was sintered in a muffle furnace at 600 °C for 2 h.
[0037] Take 2g of sample and ultrasonically disperse it in 20ml of distilled water, add dropwise chloropalladium acid solution at a molar ratio of Pd:W of 2%, adjust its pH value to 9 with ammonia water, continue to stir for 2h, and then plac...
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