A kind of silver/carbon nanotube composite material and its preparation method and application
A technology of composite materials and carbon nanotubes, applied in the direction of material electrochemical variables, structural parts, electrical components, etc., can solve problems such as high specific surface area, uneven distribution, weak combination of silver nanoparticles and carbon materials, and achieve high The effect of specific surface area, high catalytic performance, and simple and easy preparation method
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Embodiment 1
[0039] (1) The sulfonated PS nanofibers were immersed in an aqueous solution of 10 mM Tris-HCl containing 2 mg / mL DA, pH=8.5, and reacted for 20 h. After the reaction, in order to remove unadhered PDA, the nanofibers were thoroughly washed several times with ultrapure water to obtain PDA-modified PS nanofibers.
[0040] (2) Immerse the PDA-modified PS nanofibers obtained in step (1) into 10 mg / mL AgNO 3 The solution was reacted for 1.5 h, washed several times with ultrapure water, and then dried in a vacuum oven at 50° C. for 8 h to obtain Ag / PDA-modified PS nanofibers.
[0041] (3) Transfer the sample obtained in step (2) to a tube furnace, raise the temperature to 800°C at a rate of 5°C / min under nitrogen atmosphere, keep it for 1h, and carry out carbonization to obtain Ag / carbon nanotube composite The material is denoted as 1-AgNPs-NCNTs.
[0042] The scanning electron microscope picture of PS nanofiber in the present embodiment is as figure 2 As shown in A, the scannin...
Embodiment 2
[0045] (1) The sulfonated PS nanofibers were immersed in an aqueous solution of 10 mM Tris-HCl containing 2 mg / mL DA, pH=8.5, and reacted for 20 h. After the reaction, in order to remove unadhered PDA, the nanofibers were thoroughly washed several times with ultrapure water to obtain PDA-modified PS nanofibers.
[0046] (2) Immerse the PDA-modified PS nanofibers obtained in step (1) into 10 mg / mL AgNO 3 React in the solution for 1.5h, wash with ultrapure water several times, and then repeatedly immerse in dopamine solution and silver nitrate solution under the same conditions. After washing, it was placed in a vacuum drying oven and dried at 50° C. for 8 hours to obtain Ag / PDA-modified PS nanofibers.
[0047] (3) Transfer the sample obtained in step (2) to a tube furnace, raise the temperature to 800°C at a rate of 5°C / min under nitrogen atmosphere, keep it for 1h, and carry out carbonization to obtain Ag / carbon nanotube composite The material is denoted as 2-AgNPs-NCNTs.
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Embodiment 3
[0056] (1) The sulfonated PS nanofibers were immersed in an aqueous solution of 10 mM Tris-HCl containing 2 mg / mL DA, pH=8.5, and reacted for 20 h. After the reaction, in order to remove unadhered PDA, the nanofibers were thoroughly washed several times with ultrapure water to obtain PDA-modified PS nanofibers.
[0057] (2) Immerse the PDA-modified PS nanofibers obtained in step (1) into 10 mg / mL AgNO 3 React in the solution for 1.5h, wash with ultrapure water for several times, and then immerse in dopamine solution and silver nitrate solution under the same conditions twice. After washing, it was placed in a vacuum drying oven and dried at 50° C. for 8 hours to obtain Ag / PDA-modified PS nanofibers.
[0058] (3) Transfer the sample obtained in step (2) to a tube furnace, raise the temperature to 800°C at a rate of 5°C / min under nitrogen atmosphere, keep it for 1h, and carry out carbonization to obtain Ag / carbon nanotube composite The material is denoted as 3-AgNPs-NCNTs.
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