Preparation of lubricant oil containing high dispersion fullerene C60
A technology of fullerene and lubricating oil, which is applied in the field of materials, can solve the problems of limiting self-lubricating effect and easy agglomeration, and achieves the effect of excellent lubricating performance
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[0020] Example 1:
[0021] The first step: Preparation of hexadecanoic acid derivative with end group azide:
[0022] Weigh 2.56g (0.01mol) of palmitic acid in a single-necked flask, adjust the reaction temperature of the system to 45℃, slowly add 2.4g thionyl chloride dropwise, magnetically stir and keep for 12h, and distill out excess chlorine under reduced pressure The sulfoxide is converted to hexadecanoyl chloride. 4g hexadecanoyl chloride was dissolved in 25ml acetone, and 3g sodium azide was dissolved in 75ml water. At 5℃, slowly add the acetone solution of hexadecanoyl chloride dropwise to the aqueous solution of sodium azide, and react at 10℃ for 6h. The white solid was filtered out with suction, rinsed with distilled water repeatedly, and dried under vacuum at 25℃ to obtain the terminal stack Nitrided palmitic acid derivative.
[0023] The second step: preparation of palmitic acid modified C 60 (Hexadecanoic acid-C 60 ):
[0024] Weigh 250mgC 60 Add to 100ml N,N'-dimethy...
Example Embodiment
[0028] Example 2:
[0029] The first step: preparation of octadecanoic acid derivative with end group azide:
[0030] Weigh 2.84g (0.01mol) of octadecanoic acid in a single-necked flask, adjust the reaction temperature of the system to 45℃, slowly add 2.4g thionyl chloride dropwise, magnetically stir and keep for 12h, and distill out excess chlorine under reduced pressure The sulfoxide is converted to octadecanoyl chloride. Dissolve 4 g of stearyl chloride in 25 ml of acetone, and dissolve 3 g of sodium azide in 75 ml of water. At 5℃, slowly add the acetone solution of stearyl chloride dropwise to the aqueous solution of sodium azide, and react at 10℃ for 6h. The white solid was filtered out with suction, rinsed with distilled water repeatedly, and dried under vacuum at 25℃ to obtain the terminal stack Nitrided octadecanoic acid derivative.
[0031] Step 2: Preparation of C modified by octadecanoic acid 60 (Stearyl acid-C 60 ):
[0032] Weigh 250mgC 60 Add to 100ml of N,N'-dimethy...
Example Embodiment
[0036] Example 3:
[0037] The first step: preparation of eicosanoid derivatives with end group azide:
[0038] Weigh 3.12g (0.01mol) of arachidic acid in a single-necked flask, adjust the reaction temperature of the system to 55℃, slowly add 3g of thionyl bromide dropwise, magnetically stir and keep for 12h, and distill out excess bromide under reduced pressure Sulfoxide to obtain eicosanyl bromide. 4g of eicosanyl bromide was dissolved in 30ml of acetone, and 3g of potassium azide was dissolved in 60ml of water. At 5°C, slowly add the acetone solution of eicosanyl bromide to the aqueous solution of potassium azide dropwise, and react at 10°C for 10 hours. The white solid was filtered out with suction, rinsed repeatedly with distilled water, and dried under vacuum at 25°C to obtain the end groups Azidated arachidic acid derivative.
[0039] Step 2: Preparation of Eicosanic Acid Modified C 60 (Eicosan-C 60 ):
[0040] Weigh 250mgC 60 Add to 100ml N,N'-dimethylformamide, and ultras...
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