Lubricating Composition Containing a Dispersant
a technology of dispersant and lubricating composition, which is applied in the preparation of carboxylic compounds, fuels, organic chemistry, etc., to achieve the effect of mitigating soot thickening
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example 1 (
Preparative Example 1 (EX1)
[0112]A 5 L 5 neck flask is charged with 1326.8 g of polyisobutylene (vinylidene content of 5-8 mol %, and number average molecular weight of about 2050) and 1044 g of hexane. A thermocouple, water condenser and two subsurface gas inlet tubes are connected to the flask. Prior to the gas inlet, two sinter gas filters, air trap and flow meter are connected. Prior to the flow meter an air trap is connected. After the condenser, a dry-ice tap, air trap, o-toluidine trap, water trap (500 mL) and caustic trap are connected. The contents of the flask are stirred for 2 hours. The flask is then heated to 65° C. and 58 g of chlorine is added over a period of 4 hours. The reaction is blown with nitrogen gas for 30 minutes, before cooling to ambient temperature. The flask is then heated to 130° C. over 4 hours to remove hexane under vacuum. The reaction yields 1293.5 g of product.
example 2 (
Preparative Example 2 (EX2)
[0113]979.4 g of the product of EX1 and 982.4 g of dodecane are charged into a 500 ml flask. The flask has a Friedrichs condenser attached and Tygon™ tubing from the condenser outlet to a caustic trap. The thermocouple is placed in a pocket to prevent corrosion and a PTFE stirrer is used. The contents of the flask are stirred for 30 minutes at 50° C. Trans-cinnamic acid (146.5 g) is then added at room temperature via a powder funnel. The resulting mixture is stirred (250 rpm) and heated to 90° C. under nitrogen. The mixture is then heated to 180° C. over 1 hour and held at 180° C. for 18 hours. The reaction is then vacuum stripped over 7 hours while increasing the temperature from 150° C. to 200° C., before cooling to ambient temperature.
example 3 (
Preparative Example 3 (EX3)
[0114]292.7 g of the product of EX1 and 250 g of dodecane are charged into a 1 L flask. The flask has a Friedrichs condenser attached and Tygon™ tubing from the condenser outlet to a caustic trap. The thermocouple is placed in a pocket to prevent corrosion and a PTFE stirrer is used. The contents of the flask are stirred for 30 minutes at 50° C. before cooling to ambient temperature. 32.5 g of phenylpropiolic acid is added in one portion. The resulting mixture is stirred (250 rpm) and heated to 90° C. under nitrogen. The mixture is then heated to 180° C. over 1.5 hour and held at 180° C. for 18 hours. The reaction is then vacuum stripped over 10 hours while increasing the temperature from 150° C. to 200° C., before cooling to ambient temperature.
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