A kind of conductive silicone elastomer based on mxene and its preparation method and application
An elastomer and silicone technology, applied in the field of conductive silicone elastomer and its preparation, can solve the problems of lack of self-healing performance, unstable material conductivity, and inability to continue application, and achieves high-efficiency room temperature self-healing ability, preparation The effect of process environmental protection and excellent electrical conductivity
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[0060] According to the present invention, a method for preparing an MXene-based conductive organosilicon elastomer, a preferred embodiment, includes the following steps:
[0061] Disperse UPy-NCO and amino-functionalized polysiloxane derivative A in dichloromethane, react at 50℃~70℃ for 12~24h, and then add carboxylic acid derivatives containing disulfide bonds after the reaction is completed Compound B was reacted at 50℃~70℃ for 6~12h to obtain polysiloxane derivative C containing multiple reversible bonds; MXenesE and carboxyl group-containing L-citrulline D were dispersed in deionized water, and heated at 100℃ The modified MXenesF was obtained by ultrasonically dispersing the modified MXenesF into the organosilicon polymer network containing the polysiloxane derivative C containing multiple reversible bonds, stirring and ultrasonicating. The MXene-based conductive silicone elastomer is obtained by shaking the reaction for 1 hour, and curing to form a film.
[0062] In ord...
Embodiment 1
[0077] 0.16 g of UPy-NCO and 10 g of branched polydimethylaminosiloxane (Mn: 2000) were mixed in a three-necked flask. The temperature was raised to 70°C, and the reaction time was 16h. 0.84g of 2,2'-dithiodibenzoic acid was added to the reactant, and the reaction continued for 4h. After the reaction is completed, the product is poured into a polytetrafluoroethylene mold, placed in a vacuum drying oven at 40° C. until constant weight, to obtain a polysiloxane containing disulfide bonds and multiple hydrogen bonds. 1g MXenes (multilayer Ti 3 C 2 ) in 15 ml of deionized solution to obtain a suspension. 0.3g L-citrulline, multilayer Ti 3 C 2 The suspension was added to a 50ml three-necked flask with a reflux device and a stirrer and mixed uniformly at 100°C. After 12h of reaction, the modified multilayer Ti was obtained. 3 C 2 . 10g of polysiloxane containing disulfide bonds and multiple hydrogen bonds was mixed with 1g of modified multilayer Ti 3 C 2 Ultrasonic dispers...
Embodiment 2
[0082] The procedure described in Example 1 was repeated, except that 0.84 g of 2,2'-dithiodibenzoic acid was replaced with 0.46 g of 2,2'-dithiodipropionic acid.
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