Light-weight broadband electromagnetic wave absorbing material and preparation method thereof
A technology for absorbing materials and electromagnetic waves, which is applied in the field of light-weight broadband electromagnetic wave absorbing materials and their preparation, can solve problems such as single use, difficult electromagnetic wave broadband and high-efficiency absorption, and achieve simple production process, good absorption effect, and strong absorption effect
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Embodiment 1
[0032] (1) Preparation of precursor
[0033] First, at room temperature, 5 g of copper nitrate trihydrate was dissolved in 60 mL of deionized water for ultrasonication, and 1.36 g of trimesic acid was dissolved in 60 mL of ethanol for ultrasonication to obtain copper nitrate trihydrate aqueous solution and trimesic acid ethanol solution respectively. Then, under the condition of electromagnetic stirring, the copper nitrate trihydrate aqueous solution was dripped into the trimesic acid ethanol solution dropwise, and then 4mL DMF was dropped dropwise to obtain a mixed solution, and after stirring for 10min, the mixed solution was poured into a stainless steel high-pressure reaction kettle , carry out solvothermal synthesis, and react at 80°C for 20h; finally, the product obtained from the reaction is washed with methanol for 3 times, centrifuged and placed in a vacuum drying oven and dried at 120°C for 12h to obtain copper trimesate (HKUST-1( Cu)).
[0034] (2) Catalytic carbon...
Embodiment 2
[0040] (1) Preparation of precursor
[0041] First, at room temperature, 5 g of copper nitrate trihydrate was dissolved in 60 mL of deionized water for ultrasonication, and 1.36 g of trimesic acid was dissolved in 60 mL of ethanol for ultrasonication to obtain copper nitrate trihydrate aqueous solution and trimesic acid ethanol solution respectively. Then, under the condition of electromagnetic stirring, the copper nitrate trihydrate aqueous solution was dropped dropwise into the trimesic acid ethanol solution, and then 4mL DMF was dropped dropwise to obtain a mixed solution, and after stirring for 10min, the mixed solution was poured into a stainless steel high-pressure reaction kettle , carried out hydrothermal synthesis, and reacted at 80°C for 20h; finally, the reaction product was washed with methanol for 3 times, centrifuged and placed in a vacuum drying oven to dry at 120°C for 12h to obtain trimesic acid copper (HKUST-1 (Cu)).
[0042] (2) Catalytic carbonization
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