Preparation method of branched polystyrene-maleic anhydride and application thereof
A technology of maleic anhydride and polystyrene, applied in chemical instruments and methods, chemical/physical processes, transportation and packaging, etc., can solve the problems of poor dispersion stability, large dispersion index, and high reaction temperature of the dispersion, and achieve The effect of controllable polymer structure and properties, good product application performance and mild polymerization conditions
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2012-02-08
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
Figure 1 Figure 2 Figure 3
Abstract
Description
technical field
[0001] The invention relates to the field of functional polymer materials, in particular to the field of styrene-maleic anhydride (SMA) copolymers. Background technique
[0002] Compared with traditional linear polymers, branched polymers have low viscosity, high density and a large number of terminal functional groups due to their highly branched structure, no entanglement between molecules, and a large number of reactive end groups. performance.
[0003] Styrene (St)-maleic anhydride (MA) copolymer has excellent heat resistance, rigidity, dimensional stability and excellent emulsification, film forming, thickening and other characteristics, and is widely used in latex coatings, water treatment agents, Adhesive modifiers, textile auxiliaries, printing inks and other fields have always been research hotspots for scholars. However, there are few reports on branched styrene maleic anhydride, and it is very challenging to develop the preparation technology of ...
Examples
Embodiment 1
[0027] Add 1.04g (10mmol) styrene, 1.176g (12mmol) maleic anhydride, 0.1g (0.67mmol) p-vinylbenzylmercaptan to a 100ml four-neck round bottom flask equipped with a thermometer, reflux condenser and stirrer , 0.232g AIBN, and then add 44g of toluene as a polymerization solvent, place the flask in a constant temperature oil bath, heat and stir to 30°C and pass N 2 After 15 minutes, close the system, raise the temperature to 65°C, and stir for 10 hours at a constant temperature. After the reaction, the product is suction-filtered and rinsed with hot toluene (about 40°C) for several times, then dissolved in acetone, and a small amount of insoluble impurities are filtered off. Dissolving, precipitating, and purifying three times were repeated and dried in a vacuum oven to obtain 2.138 g of branched polystyrene maleic anhydride product with a monomer conversion rate of 92.3%.
Embodiment 2
[0029] Add 1.04g (10mmol) styrene, 1.176g (12mmol) maleic anhydride, 0.2g (1.34mmo) p-vinylbenzylmercaptan to a 100ml four-neck round bottom flask equipped with a thermometer, a reflux condenser and a stirrer , 0.29g AIBN, and then add 46g of toluene as the polymerization solvent, place the flask in a constant temperature oil bath, heat and stir to 35°C and pass N 2 After 20 minutes, close the system, raise the temperature to 70°C, and stir at constant temperature for 15 hours. After the reaction, the product is suction filtered and washed with hot toluene (about 40°C) for several times, then dissolved in acetone, and a small amount of insoluble impurities are filtered off. Precipitate and separate with toluene. After repeated dissolution, precipitation, and purification three times, vacuum oven drying obtained 2.160 g of branched polystyrene maleic anhydride product, and the monomer conversion rate was 89.4%.
Embodiment 3
[0031] Add 1.04g (10mmol) styrene, 1.176g (12mmol) maleic anhydride, 0.3g (2mmol) p-vinylbenzylmercaptan, 0.327g AIBN, and then add 35g of toluene as polymerization solvent, place the flask in a constant temperature oil bath, heat and stir to 40°C and turn on N 2 After 25 minutes, close the system, raise the temperature to 75°C, and stir for 20 hours at a constant temperature. After the reaction, the product is suction filtered and washed with hot toluene (about 40°C) for several times, then dissolved in acetone, and a small amount of insoluble impurities are filtered off. Precipitate and separate with toluene. After repeated dissolution, precipitation, and purification three times, vacuum oven drying obtained 2.204 g of branched polystyrene maleic anhydride product, and the monomer conversion rate was 87.6%.