Alkylphenolate detergent, preparation method and applications thereof
A technology of alkyl phenate and detergent, applied in the field of lubricating oil detergent, can solve problems such as limited rust preventive effect, and achieve the effects of improving post-treatment efficiency, improving phase separation problem, and improving rust preventive performance.
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[0023] The embodiment of the present invention discloses a preparation method of an alkylphenate detergent, comprising:
[0024] a) Alkylphenol, basic compound, coupling reagent and solid acid are mixed with optional diluent and / or accelerator for coupling reaction;
[0025] b) adding basic compounds, and passing carbon dioxide to carry out carbonation reaction;
[0026] c) Separation to obtain the target product.
[0027] In the above preparation method, the alkylphenol is obtained by using one or more C containing monomers from the hydroxyaromatic compound 8 -C 45 Oligomers obtained by alkylation of olefins, said monomers being selected from propylene, butene or mixtures thereof.
[0028] In the above preparation method, the basic compound may be preferably selected from but not limited to alkali metal oxides, alkali metal hydroxides, alkali metal carbonates, alkaline earth metal oxides, alkaline earth metal hydroxides, alkaline earth metal carbonates or their mixture. ...
Embodiment 1
[0059] Add dodecylphenol (49.5 g), base oil (37.5 g), p-toluenesulfonic acid activated clay (24.75 g) and isooctyl alcohol (30 mL) into the reactor successively under argon atmosphere, and stir After bubbling argon through and heating the mixture to 60°C, sulfur (11 g) and calcium hydroxide (54.7 g) were added. The temperature of the mixture was raised to 150ºC, and ethylene glycol (10 g) was added. The temperature was further raised to 175ºC, and the reaction was stirred at this temperature for 3h. Stop blowing argon, and blow carbon dioxide (40 mL / min) into the reaction liquid for 5h. Then the mixture was distilled under high vacuum and reduced pressure for 1 hour at 150°C to distill off the solvent and water. The vacuum distillation was stopped and additional base oil (22g) was added. The mixture was stirred for 15 minutes, and hot filtered to obtain the total base number TBN of the sulfurized dodecylphenol calcium salt detergent: 294 mgKOH / g.
Embodiment 2
[0061] Dodecylphenol (main component is p-dodecylphenol) (30g), base oil (36.5g), clay activated by dodecylbenzenesulfonic acid (18g) and Isooctyl alcohol (50 mL) was successively added into the reactor, argon was bubbled under stirring, and the mixture was heated to 60°C, then formaldehyde (11 g) and calcium hydroxide (34.2 g) were added. The temperature of the mixture was raised to 160ºC, and ethylene glycol (10 g) was added. The temperature was further raised to 180ºC, and the reaction was stirred at this temperature for 3h. Stop argon blowing, and blow carbon dioxide (40 mL / min) into the reaction solution for 6 h. Then the mixture was distilled under high vacuum and reduced pressure for 1 h at 150ºC to distill off the solvent and water. The vacuum distillation was stopped and additional base oil (18 g) was added. The mixture was stirred for 15 minutes, and filtered hot to obtain the total base number TBN of the dodecylphenol calcium salt detergent: 239 mg KOH / g.
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