Emulsion cutting fluid composition
A technology of composition and cutting fluid, applied in the direction of lubricating composition, petroleum industry, etc., can solve the problems of influence of filtration system, poor on-site sanitation, increased consumption of filter paper, etc.
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Embodiment 1
[0055] Example 1 Synthesis of polyisobutylene o-cresol
[0056] In a 500ml four-necked flask equipped with a stirrer, thermometer, condenser and dropping funnel, add 34.93g (0.323mol) o-cresol, 6.88g (0.048mol) boron trifluoride ether catalyst, and 100ml n-hexane solvent React with 161.61g (0.162mol) of polyisobutylene (Mn=1000) at 80°C for 2h. After the reaction, the reaction mixture was washed once with 5% potassium hydroxide solution, and washed with hot water until neutral to remove the catalyst, and then the solvent and unreacted o-cresol were removed by distillation under reduced pressure. The hydroxyl value of the synthetic product polyisobutylene o-cresol was 53.49 mg / g. The determination of hydroxyl value refers to the acetic anhydride method in GB / T7383-2007.
[0057] An example reaction is as follows:
[0058]
Embodiment 2
[0060] The polyisobutylene o-cresol 47.16g (0.045mol) obtained in Example 1 was added to a 500ml four-neck beaker equipped with a stirrer, a thermometer and a separator under nitrogen protection, and then 2.70g (0.045mol) was added. ethylenediamine, 3.83g (0.047mol) formaldehyde, and 47ml of toluene was added as a reaction solvent. After reacting at 80°C for 1.5h, the temperature was lowered to room temperature, and 4.17g (0.0225mol) of p-hydroxydiphenylamine, 3.83g ( 0.047mol) formaldehyde, react at 70°C for 1h. After the reaction is completed, the solvent and a small amount of water generated are distilled off under reduced pressure to obtain the final Mannich base detergent. An example reaction is as follows:
[0061]
[0062] or a small amount
[0063]
Embodiment 3
[0065] The polyisobutylene o-cresol 53.37g (0.051mol) prepared in Example 1 was added to a 500ml four-neck beaker equipped with a stirrer, a thermometer and a separator under nitrogen protection, and then 7.46g (0.051mol) was added. of triethylenetetramine, 4.38g (0.054mol) formaldehyde, and 54ml of xylene was added as a reaction solvent. After reacting at 100°C for 1.5h, the temperature was cooled to room temperature, and 5.87g (0.0255mol) of 4-hydroxy-2'- Nitrodiphenylamine, 4.38g (0.054mol) formaldehyde, react at 80°C for 1h. After the reaction is completed, the solvent and a small amount of water generated are distilled off under reduced pressure to obtain the final Mannich base detergent. Refer to Example 2 for an example reaction.
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