Base oil for refrigerator oil, preparation method and application of base oil for refrigerator oil
A technology for refrigerating machine oil and base oil, which is applied in the direction of base material, petroleum industry, lubricating composition, etc. It can solve the problems of difficult removal, low catalyst selectivity, and many by-products, and achieves easy operation, favorable industrial production, and low by-product low effect
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Embodiment 1
[0024] Step (1): Weigh 28.2g of trimethylolpropane, 100g of nonanoic acid, and 0.11g of silicon phosphate in the reaction kettle, vacuumize, start stirring, and then slowly heat up to 180°C. After the temperature rises to 180°C, keep The kettle pressure is -0.095MPa≤vacuum degree≤-0.085MPa. The distillation unit distills the water generated by the reaction.
[0025] Step (2): After maintaining the reaction for 4.5 hours, weigh the quality of the produced water to estimate the reaction is over, cool to 60-80°C, remove silicon phosphate by suction filtration while it is hot, and obtain a light yellow oily liquid which is trimethylolpropane nonanoic acid ester. Tested by an elemental analysis instrument, the theoretically synthesized product is C 33 h 62 o 6 , the mass fraction of carbon element is 71.48% in theory, 71.51% in reality; the mass fraction of hydrogen element is 11.12% in theory, and 11.03% in reality. It is found that the experimental value is consistent with th...
Embodiment 2
[0028] Step (1): Weigh 28.2g of trimethylolpropane, 35.9g of hexanoic acid, 64g of lauric acid, and 0.13g of silicon phosphate in the reaction kettle, vacuumize, start stirring, then slowly heat up to 180°C, and the temperature rises to After 180°C, keep the kettle pressure at -0.095MPa≤vacuum degree≤-0.085MPa. The distillation unit distills the water generated by the reaction.
[0029] Step (2): After maintaining the reaction for 4.5 hours, weigh the quality of the produced water to estimate the end of the reaction, cool to 60-80°C, remove the solid catalyst by suction filtration while it is hot, and obtain a light yellow oily liquid that is trimethylolpropane hexanoic acid laurate. Tested by an elemental analysis instrument, the theoretically synthesized product is C 33 h 62 o 6 , the mass fraction of carbon element is theoretically 71.48%, and the actual value is 71.54%; the theoretical mass fraction of hydrogen element is 11.12%, and the actual value is 11.00%.
[003...
Embodiment 3
[0032] Step (1): Weigh 28.2g of trimethylolpropane, 46.4g of hexanoic acid, 65.3g of stearic acid, and 0.13g of silicon phosphate in the reaction kettle, vacuumize, start stirring, and then slowly heat up to 180°C. After rising to 180°C, keep the kettle pressure at -0.095MPa≤vacuum degree≤-0.085MPa. The distillation unit distills the water generated by the reaction.
[0033] Step 2: After maintaining the reaction for 4.5 hours, weigh the quality of the produced water to estimate the reaction is over, cool to 60-80°C, remove silicon phosphate by suction filtration while it is hot, and obtain a light yellow oily liquid which is trimethylolpropane stearyl hexanoate esters. Tested by an elemental analysis instrument, the theoretically synthesized product is C 37 h 70 o 6 , the mass fraction of carbon element is theoretically 72.79%, and the actual value is 72.70%; the theoretical mass fraction of hydrogen element is 11.48%, and the actual value is 11.37%.
[0034] The acid va...
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