Synthesis process of novel lubricant pour point depressant
A synthesis process and lubricant technology, applied in the direction of lubricating compositions, etc., can solve the problems such as limiting the scope of application of pour point depressants, and achieve the effects of high synthesis rate, high purity and good application prospects
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2012-09-26
- Estimated Expiration
- Not applicable · inactive patent
Abstract
Description
technical field
[0001] The invention relates to the field of chemical synthesis, in particular to a synthesis process of a novel lubricant pour point depressant. Background technique
[0002] The distribution of n-alkanes in oil products is the main factor affecting the effect of pour point depressant, and there is a certain correspondence between the distribution of n-alkanes and the length of the ester chain of the pour point depressant. There is an optimal value for the carbon number of the ester side chain of a single type of pour point depressant, and at the same time, it has pour point depressant selectivity for different oil products, which limits the scope of application of a single pour point depressant. The pour point depressants with different chemical compositions are compounded to improve the pour point depressant effect through the coordination effect, which can expand the application range of the pour point depressants. Contents of the invention
[0003] Th...
Examples
Embodiment Construction
[0012] A synthetic process of a novel lubricant pour point depressant,
[0013] 1. Synthesis of Higher Alcohol Acrylate
[0014] Reagents and specifications: high carbon alcohol, anhydrous calcium chloride, analytical alcohol; acrylic acid, chemically pure; methanol, analytically pure.
[0015] Specific steps: In a three-neck flask equipped with a reflux condenser, a thermometer and an agitator, add measured amounts of higher alcohol and a polymerization inhibitor, heat to a certain temperature to completely melt the higher alcohol, and then add acrylic acid and catalyst in sequence. The mixture was first heated to reflux at 110-120°C for about 2.5 hours, and then gradually raised to 140°C for about 6 hours to obtain the product crude ester. Remove the unreacted unsaturated acid and residual water in the crude ester by distillation under reduced pressure, wash the acidic catalyst and polymerization inhibitor with a weak alkali solution with a mole fraction of 0.2% at a temper...