Carbon nanotube and carbon nanofiber synergetic enhanced copper base composite material and preparation method
A copper-based composite material and surface modification technology, applied in the field of composite materials, can solve problems such as difficult interface bonding, poor wettability of metal matrix, easy aggregation and accumulation, etc.
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Embodiment 1
[0055] Add CNTs to 10μg / ml gallic acid aqueous solution, and disperse evenly, wherein the ratio of the weight of CNTs to the volume of gallic acid aqueous solution is 0.1g:40ml; let it stand for 24h, filter, take the filter residue and dry it in vacuum at 60°C for 2h, Surface-modified CNTs were obtained.
[0056] Evenly disperse 0.1 g of the surface-modified CNTs prepared in this example in 100 ml of deionized water, and after standing for 3 days, the precipitation gradually increases under the action of gravity, but the CNTs still maintain a dispersed state without agglomeration; at the same time Compared with unmodified CNTs, precipitation occurred after standing for 1 day, and agglomeration occurred among CNTs, indicating that the surface-modified CNTs prepared in Example 1 had excellent dispersibility.
[0057] Using the above-mentioned method, the modified carbon nanotubes were prepared by successively using gallic acid aqueous solutions with a concentration of 5 μg / ml an...
Embodiment 2
[0061] Add CNFs to 0.02μg / ml rutin aqueous solution, and disperse evenly. The ratio of the weight of CNFs to the volume of rutin aqueous solution is 0.1g:40ml; let it stand for 24h, filter, and take the filter residue and dry it in vacuum at 60°C for 2h , to obtain surface-modified CNFs.
[0062] Evenly disperse 0.1 g of the surface-modified CNFs prepared in Example 2 in 100 ml of deionized water. After standing for 5 days, the precipitation gradually increases under the action of gravity, but the CNFs still maintain a dispersed state without agglomeration; At the same time, compared with unmodified CNFs, precipitation occurred after standing for 1 day, and agglomeration occurred between CNFs, indicating that the surface-modified CNFs prepared in Example 2 had excellent dispersibility.
[0063] Using the above method, the modified carbon nanofibers (CNFs) were prepared sequentially with rutin aqueous solutions with concentrations of 0.2 μg / ml and 2 μg / ml, and Fourier transform...
Embodiment 3
[0066] (1) Get the surface-modified CNTs and the surface-modified CNFs (both the modified CNTs and the modified CNFs with the best performance prepared in Example 1-2) prepared in Example 1 and Example 2, That is, 10 μg / ml gallic acid, 0.02 μg / ml rutin modified CNTs and CNFs, the following examples are the same); (2) in parts by weight, adopt agate balls and agate ball jars to mix 0.8 parts of CNTs and 0.2 parts of CNFs, 3 parts graphite powder, 10 parts Ti 3 SiC 2 powder, 0.1 part of La powder and 85.9 parts of copper powder were mixed by ball milling, the speed of rotation was 200 rpm, and the ball milling time was 50 min, so that the powder was mixed evenly to obtain a composite powder; (3) the composite powder was hot-pressed and sintered for 2 hours, and then Pressing and sintering at a temperature of 950°C and a pressure of 28MPa, cooling with the furnace to obtain a copper-based composite block material; (4) subjecting the obtained block material to hot isostatic press...
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