Vulcanized thiophosphonate sulfide compound as well as preparation method and application thereof
A technology of phosphonate and compound, which is applied in the field of sulfurized phosphonothioate compound, can solve the problem of inconsistent development trend, inability to measure anti-wear performance and load-bearing capacity, lack of extreme-pressure anti-wear agent load-bearing capacity and resistance Grinding performance and other issues
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Embodiment 1
[0063] The preparation of embodiment 1 sulfurized cardanol
[0064] Put 62g of cardanol (about 0.2mol) and 12.8g of sulfur powder (0.4mol) into a 250ml three-necked reaction flask, start stirring and heating. The reaction temperature was maintained at 190° C., and the reaction was continued for 3 hours. After the reaction was completed, the temperature was lowered, and a dark brown-red viscous liquid was obtained after filtration, which was cardanol sulfide, and the conversion rate of the product was 89.3%.
Embodiment 2
[0065]The preparation of embodiment 2 phenylthiophosphonic acid cardanol ester
[0066] Add 20g of cardanol, 4g of triethylamine and 20g of toluene into the reaction flask, start heating and stirring, add 7.5g of phenylphosphonothioate dichloride, maintain the reaction temperature at 70°C, and react for 5 hours. After the reaction, the temperature was lowered to obtain a brown-red transparent liquid. The reaction product was washed with distilled water until neutral, and the organic phase was distilled under reduced pressure at 100 Pa and 150° C. for 1 h to remove water and solvent to obtain a brownish-yellow transparent liquid with a conversion rate of 94.8%.
Embodiment 3
[0067] The preparation of embodiment 3 phenylthiophosphonic acid cardanol disulfide
[0068] Add 25g of sulfurized cardanol prepared in Example 1, 8g of triethylamine and 50g of toluene into the reaction flask, start heating and stirring, add 5g of phenylphosphonothioate dichloride, maintain the reaction temperature at 90°C, and react for 4 hours . After the reaction, the temperature was lowered to obtain a brown-red transparent liquid. The reaction product was washed with distilled water until neutral, and the organic phase was distilled under reduced pressure at 100 Pa and 150° C. for 1 h to remove water and solvent to obtain a brownish-yellow transparent liquid with a conversion rate of 95.1%.
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