MOFs carbonized product, preparation method and application to modification of lead-free solder
A lead-free solder and product technology, applied in the field of materials, can solve the problems of limitation of modification effect, increase of composite solder defects, affecting the performance of matrix solder, etc., and achieve the effect of avoiding agglomeration
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[0018] A kind of preparation method of the lead-free solder modifier based on MOFs carbonization product of the present invention, comprises the following steps:
[0019] (1) Preparation of MOFs;
[0020] Mix the nitrate as the metal particle source, the organic ligand, and the liquid as the reaction condition according to the molar ratio of 1:(4-16):(4-16), and ultrasonically stir the mixed solution at room temperature for 10-20min; Then put the solution into a reaction kettle and place it in an oven at a temperature of 100-150°C for 12-24h, centrifuge and filter the resulting precipitate with absolute ethanol, and finally dry it under an environment of 70-100°C for 12-24h , to obtain the dodecahedral, layered or flake MOFs powder with a particle size of 100nm-1μm.
[0021] (2) Carbonization treatment:
[0022] Put the MOFs powder obtained in step (1) in the tube furnace to set the temperature rise curve, make the tube furnace heat up at 3-6°C / min under the protection of ar...
Embodiment 1
[0030] (1) Synthesis of ZIF-67
[0031] Weigh 0.5gCo(NO 3 ) 2 ·6H 2 O was dissolved in 50mL deionized water to form A solution; 2-methylimidazole and triethylamine (TEA) were weighed and dissolved in 50mL deionized water to form B solution; A and B solutions were ultrasonically stirred for 10min and then mixed; wherein, Co (NO 3 ) 2 ·6H 2 The molar ratio of O, 2-methylimidazole and triethylamine (TEA) is 1:16:16; the mixed solution was ultrasonically stirred at room temperature for 10 minutes, and then the solution was placed in a reaction vessel at a temperature of 120°C. After reacting in an oven for 24 hours, the obtained precipitate was centrifuged and filtered with absolute ethanol, and finally placed in an oven at a temperature of 70° C. for 12 hours to obtain ZIF-67 powder.
[0032] (2) Carbonization treatment
[0033] The ZIF-67 powder obtained in step (1) was placed in a tube furnace, and the tube furnace was heated at a rate of 5°C / min under the protection of ...
Embodiment 2
[0037] (1) Synthesis of ZIF-67
[0038] Weigh 0.5gCo(NO 3 ) 2 ·6H 2 O was dissolved in 50mL deionized water to form A solution; 2-methylimidazole and triethylamine (TEA) were weighed and dissolved in 50mL deionized water to form B solution; A and B solutions were ultrasonically stirred for 10min and then mixed; wherein, Co (NO 3 ) 2 ·6H 2The molar ratio of O, 2-methylimidazole and triethylamine (TEA) is 1:16:16; the mixed solution was ultrasonically stirred at room temperature for 10 minutes and then washed 2-3 times with deionized water, and then the solution was loaded into The reaction kettle was placed in an oven at a temperature of 100°C for 18 hours, the obtained precipitate was centrifuged and filtered with absolute ethanol, and finally dried in an oven at a temperature of 70°C for 12 hours to obtain ZIF-67 powder.
[0039] (2) Carbonization treatment
[0040] The ZIF-67 powder obtained in step (1) was placed in a tube furnace, and the tube furnace was heated at ...
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