A kind of sulfur phosphorus nitrogen boron type extreme pressure antiwear agent, its preparation method and gear oil
An extreme pressure anti-wear agent, sulfur phosphorus nitrogen technology, used in additives, petroleum industry, lubricating compositions, etc., can solve the problems of easy to cause corrosion, high sulfur content, ineffectiveness, etc., achieve low sulfur content, The effect of improving the bearing capacity and reducing the dosage
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[0031] A sulfur, phosphorus, nitrogen, and boron type extreme pressure antiwear agent has the following structural formula:
[0032] , where R 1 for C 4 -C 12 Alkyl, R 2 for C 4 -C 20 Alkyl, R 3 for hydrogen or C 4 -C 12 Alkyl, R 4 for hydrogen or C 1 -C 8 the alkyl group, R 5 for hydrogen or C 1 -C 8 the alkyl group, R 6 for hydrogen or C 1 -C 8 of alkyl.
[0033]A preparation method of a sulfur-phosphorus-nitrogen-boron type extreme pressure antiwear agent is prepared by using the following parts by mass in a mixed solution of water and an organic solvent: 1 part of sulfur phosphorus compound; 1.2 to 1.5 parts of alcohol compound; 1.0-2.0 parts of amine compounds; 1.0-1.5 parts of benzotriazole or benzotriazole derivatives; 1.0-1.5 parts of boron compounds; among them, the water and organic solvent in the mixed liquid of water and organic solvent are of any mass Compare.
[0034] Wherein, the sulfur phosphorus compound may be phosphorus trichloride; the ...
example 1
[0040] First connect the stirring device, the condensing device and the reactor, and add phosphorus trichloride, isobutanol (or C 4 -C 6 branched or straight-chain alcohol), water, benzene or toluene or xylene, after fully stirring, react at 10°C for 6 hours, and distill at atmospheric pressure to obtain the intermediate product A1.
[0041] The intermediate product A1 is mixed with appropriate amount of benzotriazole, tert-butylamine (or C 4 -C 8 straight-chain or branched aliphatic primary amine), benzene or toluene or xylene, stir well, and react at 60°C for 2 hours to obtain the intermediate product B1.
[0042] The intermediate product B1 and boric acid were fully stirred evenly, heated to reflux for 3 hours, the solvent was distilled off under normal pressure, and the final product C1 was obtained by filtration.
[0043] The structural formula of product C1 is:
[0044] .
example 2
[0046] First connect the stirring device, the condensing device and the reactor, and add phosphorus trichloride, n-octanol (or C 7 -C 10 branched or straight-chain alcohol), water, n-heptane or solvent gasoline, after fully stirring, react at 50°C for 2 hours, and distill at atmospheric pressure to obtain the intermediate product A2.
[0047] The intermediate product A2 and the appropriate amount of butyl benzotriazole (or benzene ring belt C 4 -C 8 straight-chain or branched-chain alkyl), dodecylamine (or C 8 -C 16 straight-chain or branched aliphatic primary amine), n-heptane or solvent gasoline, stir well, and react at 60°C for 2 hours to obtain the intermediate product B2.
[0048] Intermediate product B2 is mixed with appropriate triethanolamine borate (or C 3 -C 16 The organoboric acid ester) was fully stirred evenly, heated to reflux for 3 hours, the solvent was distilled off under normal pressure, and the final product C2 was obtained by filtration.
[0049] The...
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