Method for modifying unsaturated polyester resin by in-situ polymerization of reactive nano-SiO2
A polyester resin, in-situ polymerization technology, applied in the field of materials, can solve the problems of application limitations, the impact performance cannot meet the requirements, etc., and achieve the effects of convenient operation, excellent mechanical properties, and simple process
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Embodiment 1
[0025] Weigh 3.0g of nano-silica RNS-E, 83.0g of maleic anhydride, 125.4g of phthalic anhydride and 141.8g of propylene glycol into the polymerization reactor. React at 160°C for 2h and at 200°C for 3h. Measure the acid value of the reaction system, when it is less than 80mgKOH / g, vacuumize for 1.2h, and the vacuum degree is 0.085Mpa. When the acid value of the reaction system drops to 40-50mgKOH / g, stop vacuuming, cool down to 180°C, add 0.075g of polymerization inhibitor hydroquinone and 0.10g of paraffin, continue to cool down to 120°C and add 165g of styrene to obtain Modified unsaturated polyester resin composite material.
[0026] Operate under the same conditions without adding nano-silica to prepare an unsaturated polyester resin; the composite material obtained in the present invention and the unsaturated polyester resin material (comparative example 1) are made according to the GB / T2567-2008 standard The splines were tested, and the results are shown in Table 1:
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Embodiment 2
[0030] Weigh 2.0 g of nano-silica RNS-A, dissolve it in 33.9 g of diethylene glycol, and oscillate ultrasonically to disperse it evenly.
[0031] Add 78.2g maleic anhydride, 118.1g phthalic anhydride, 109.2g propylene glycol and diethylene glycol dispersed with RNS-A into the polymer reactor, react at 160°C for 2h, and react at 200°C for 3h. When the acid value of the reaction system reaches 70-80mgKOH / g, vacuumize for 1.5h, and the vacuum degree is 0.09Mpa. When the acid value of the reaction system drops to 30-40mgKOH / g, stop vacuuming, cool down to 180°C and add 0.075g of inhibitor hydroquinone and 0.10g of paraffin. Continue to lower the temperature to 120° C. and add 175 g of styrene to obtain a modified unsaturated polyester resin composite material.
[0032] Operate under the same conditions without adding nano-silica to prepare an unsaturated polyester resin; the composite material obtained in the present invention and the unsaturated polyester resin material (compara...
Embodiment 3
[0036] Weigh 3g of nano-silica RNS-D, dissolve it in propylene glycol, and vibrate ultrasonically to make it completely dispersed.
[0037]115.6 g maleic anhydride, 87.3 g phthalic anhydride, and 148.0 g propylene glycol with RNS-D were charged to the polymer kettle. React at 160°C for 2h and at 200°C for 3h. Measure the acid value of the reaction system, and when it reaches 70-80mgKOH / g, vacuumize for 1.5h, and the vacuum degree is 0.085Mpa. When the acid value of the reaction system drops to 30-40mgKOH / g, stop vacuuming, cool down to 180°C and add 0.075g of inhibitor hydroquinone and 0.10g of paraffin. Continue to lower the temperature to 120° C. and add 165 g of styrene to obtain a modified unsaturated polyester resin composite material.
[0038] Operate under the same conditions without adding nano-silica to prepare an unsaturated polyester resin; the composite material obtained in the present invention and the unsaturated polyester resin material (comparative example 3)...
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