Nano core-shell compound and composite fiber membrane for photothermal enhanced degradation of chemical warfare agent simulants and preparation methods and application of nano core-shell compound and composite fiber membrane
A composite fiber membrane and nano-core-shell technology, which is applied in the field of catalytic chemistry, can solve the problems of complex and harsh fiber membrane preparation methods, unfavorable practical use of catalysts, and difficulty in achieving scale, so as to solve the problems of reduced catalytic performance, long-term challenges, and improved The effect of catalytic efficiency
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[0069] Example 1
[0070] A method for preparing a nano-core-shell composite for photothermal enhanced degradation of chemical warfare agent simulants, the steps are as follows:
[0071] (1) Preparation of photothermal agent
[0072] 90mL of water, 40mL of ethanol and 2mL of ammonia were mixed and stirred for 30 minutes to obtain a mixed solution. Weigh 0.5g of dopamine hydrochloride and dissolve in 10mL of water and add to the mixed solution. Stir continuously at 30°C for 24h. After the reaction, the solid was collected by centrifugation and deionized. Wash with water three times to obtain the photothermal agent dopamine melanin nanoparticles (Dpa NPs);
[0073] (2) Preparation of nano core-shell composite
[0074] Weigh 7mg of Dpa NPs in step (1) and disperse it in 50mL N,N-dimethylformamide, add 1.3mmol of zirconium chloride, stir for 5h at room temperature to obtain a dispersion, the purpose is to adsorb zirconium ions on the surface of Dpa NPs ; Add 1.3mmol 2-aminoterephthalic ac...
Example Embodiment
[0083] Example 2
[0084] A method for preparing a composite fiber membrane for photothermal enhancement and degradation of chemical warfare agent simulants, the steps are as follows:
[0085] (1) Preparation of spinning solution
[0086] 0.6g Dpa@UiO-66-NH prepared in Example 1 2 Disperse uniformly in 3.6g N,N-dimethylformamide solution, then add 0.4g polyacrylonitrile and stir for 12h, mix evenly to obtain spinning solution; wherein the weight average molecular weight of polyacrylonitrile is 150,000;
[0087] (2) Preparation of composite fiber membrane
[0088] Electrospin the spinning solution obtained in step (1) under spinning conditions: spinning voltage of 16kV, electrode distance of 180mm, temperature of 30°C, and relative humidity of 10% to obtain a composite fiber membrane, namely Dpa@UiO-66 -NH 2 / PAN.
[0089] The composite fiber membrane Dpa@UiO-66-NH prepared in this example 2 / PAN SEM image such as Picture 9 As shown, the diameter of the fiber is 0.5-3 μm.
[0090] The co...
Example Embodiment
[0111] Experimental example 1
[0112] The products obtained in Example 1 and Comparative Examples 1-2 were subjected to the degradation experiment of the chemical warfare agent simulant dimethyl pyrifen (DMNP) under the conditions of no near-infrared laser and near-infrared laser. The specific steps are as follows: room temperature Next, 6.7-7.7 mg of the above powder sample and 1 mL of 0.45 M N-ethylmorpholine aqueous solution were vigorously stirred in a 7 mL quartz test tube for 30 minutes, and then the test tubes were placed in a dark box with a near-infrared laser and no light source, and Place circulating water around it to keep the temperature at 25°C. Add 4μL of DMNP to the above mixed solution and continue to stir. Take out 20μL of the solution and dilute it in 0.15M N-ethylmorpholine aqueous solution at regular intervals. Use an ultraviolet-visible spectrophotometer to detect the absorbance of each sample to obtain Figure 16-18 Conversion curve of DMNP shown.
[0113] ...
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