MAX@M composite electrical contact reinforced phase material, composite electrical contact material and preparation method
A technology of electrical contact material and enhanced phase, applied in the direction of contacts, circuits, electrical switches, etc., can solve the problems of poor Ag/Ni anti-welding performance, large material transfer, and reduced workability due to the tendency of melting and welding.
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[0033] The preparation method of the reinforced phase material of the composite electric contact is specifically to sensitize the matrix MAX phase material in an acidic environment to generate MXene in situ on its surface, generate active MXene sites after activation treatment, and then coat the surface with chemical plating metal nanoparticles;
[0034] The MXene material is generated in situ on the surface of the sensitized matrix MAX material, and after activation, the surface-coated metal nanoparticle MAX@M is formed by electroless plating. The process is simple and can be carried out at room temperature, and the practical applicability is high. After covering the surface of MAX@M, the performance of the material is greatly improved.
[0035] Specifically, the preparation method of the composite electrical contact reinforcement phase material includes the following steps:
[0036] S1: Weigh the MAX powder and add the acid solution, and put them together in a cylindrical r...
Embodiment 1
[0051] According to liquid: solid=10:1 mass ratio will 10gTi 3 SiC 2 Add the powder into the HF acid solution with a concentration of 10wt%, stir in a magnetic stirrer at a temperature of 30°C at a speed of 30rpm for 1 hour; use a 10mL centrifuge tube to take the mixture, and set the centrifuge at a speed of 600rpm The material was centrifuged for 1 hour, and the mixture was subjected to centrifugation and freeze-dried for 1 hour to remove moisture to obtain a surface-generated Ti 3 C 2 site Ti 3 SiC 2 powder; the mixed powder is immersed in a concentration of 10 wt% PdCl 2 In the activator for 1 hour, put in AgNO with a concentration of 20wt% after filtration 3 、CH 3 OH, HCHO, NaOH, EDTA-2Na, C 4 h 4 o 6 KNa·4H 2 O, K 4 [Fe(CN 6 )]·3H 2 O mixed solution was stirred at 50 rpm for 1 h, the nanocomposite powder was washed with deionized water until the deionized water was transparent, and the nanocomposite powder was taken out and dried at 30° C. for 1 h. That is, ...
Embodiment 2
[0054] By liquid: solid=20:1 mass ratio will 20gTi 3 SiC 2 Add the powder into the HF acid solution with a concentration of 20wt%, stir in a magnetic stirrer at a temperature of 40°C at a speed of 50rpm for 4 hours; use a 10mL centrifuge tube to take the mixture, and set the centrifuge at a speed of 1500rpm The material was centrifuged for 2 hours, and the mixture was subjected to centrifugation and freeze-dried for 2 hours to remove moisture to obtain a surface-generated Ti 3 C 2 site Ti 3 SiC 2 powder; the mixed powder is immersed in a concentration of 20 wt% PdCl 2 1.5 hours in the activator, put into the CuSO concentration after filtering and be 30wt% 4 ·5H 2 O, CH 3 OH, HCHO, NaOH, EDTA-2Na, C 4 h 4 o 6 KNa·4H 2 O, K 4 [Fe(CN 6 )]·3H 2O mixed solution was stirred at 100rpm for 2h, the nanocomposite powder was washed with deionized water until the deionized water was transparent, and the nanocomposite powder was taken out and dried at 40°C for 2h. That is, t...
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