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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Embodiment 1
[0021] The first step: preparation of hexadecanoic acid derivatives with terminal azidation:
[0022] Weigh 2.56g (0.01mol) of palmitic acid and place it in a single-necked bottle, adjust the reaction temperature of the system to 45°C, slowly add 2.4g of thionyl chloride dropwise, magnetically stir and keep warm for 12h, and distill off excess chlorine under reduced pressure sulfoxide to give hexadecanoyl chloride. Dissolve 4g of hexadecanoyl chloride in 25ml of acetone, and dissolve 3g of sodium azide in 75ml of water. At 5°C, the acetone solution of hexadecanoyl chloride was slowly added dropwise to the aqueous solution of sodium azide, reacted at 10°C for 6 hours, the white solid was filtered out with suction, rinsed repeatedly with distilled water, and dried in vacuum at 25°C to obtain the terminal azide Nitrided hexadecanoic acid derivatives.
[0023] Step 2: Preparation of hexadecanoic acid-modified C 60 (Hexadecanoic Acid-C 60 ):
[0024] Weigh 250mgC 60 Add to 10...
Embodiment 2
[0029] The first step: preparation of octadecanoic acid derivatives with terminal azidation:
[0030] Weigh 2.84g (0.01mol) of octadecanoic acid and place it in a single-necked bottle, adjust the reaction temperature of the system to 45°C, slowly add 2.4g of thionyl chloride dropwise, magnetically stir and keep warm for 12h, and distill off excess chlorine under reduced pressure sulfoxide to obtain octadecanoyl chloride. Dissolve 4g of octadecanoyl chloride in 25ml of acetone, and dissolve 3g of sodium azide in 75ml of water. At 5°C, the acetone solution of octadecanoyl chloride was slowly added dropwise to the aqueous solution of sodium azide, reacted at 10°C for 6 hours, and the white solid was filtered out with suction, rinsed repeatedly with distilled water, and dried in vacuum at 25°C to obtain terminal azide Nitrided octadecanoic acid derivatives.
[0031] Step 2: Preparation of octadecanoic acid-modified C 60 (octadecanoic acid-C 60 ):
[0032] Weigh 250mgC 60 Add...
Embodiment 3
[0037] Step 1: Preparation of eicosanic acid derivatives with terminal azidation:
[0038] Weigh 3.12g (0.01mol) of eicosanic acid and place it in a single-necked bottle, adjust the reaction temperature of the system to 55°C, slowly add 3g of thionyl bromide dropwise, stir magnetically and keep it warm for 12h, distill off excess bromide Sulfoxide to obtain eicosyl bromide. Dissolve 4g of eicosyl bromide in 30ml of acetone, and dissolve 3g of potassium azide in 60ml of water. At 5°C, the acetone solution of eicosyl bromide was slowly added dropwise to the aqueous solution of potassium azide, reacted at 10°C for 10 hours, the white solid was filtered out by suction, rinsed repeatedly with distilled water, and dried in vacuum at 25°C to obtain the end group Azidated Eicosanic Acid Derivatives.
[0039] Step 2: Preparation of eicosanic acid-modified C 60 (eicosanic acid-C 60 ):
[0040] Weigh 250mgC 60 Add to 100ml N,N'-dimethylformamide, ultrasonically disperse for 0.3h. ...
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