Organosilicon-modified PVC composite material
A composite material and silicone technology, applied in the field of silicone modified PVC composite materials, can solve the problems of poor controllability of the graft rate and crosslinking density of PVC materials, difficulty in obtaining silicone modified PVC materials, and poor compatibility. , to achieve the effect of excellent low temperature resistance, long service life and stable performance
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Embodiment 1
[0021] (1) Add 1000 g of trimethylbenzene, 400 g of deionized water and 58.8 g of 0.1 mol / L trifluoromethanesulfonic acid into a 3 L clean three-necked flask, add dropwise from 39.5 g acryloyloxytrimethylsilane, 208 g ethyl orthosilicate, 240 g dimethyldiethoxysilane, 100 g methyltrimethoxysilane and 16.2 g hexamethyldisiloxane, dropwise After completion, the temperature was raised to 40 °C for 4 h, and the layers were separated. After the oil phase was washed to neutrality, the organic solvent and low molecular weight were removed under reduced pressure at 180 °C / 20 mm Hg to obtain 260 g of acryloyloxy-containing Silicone polymer material.
[0022] (2) Take 100g of the vinyl-terminated, acryloyloxy-containing silicone polymer material obtained in (1), 1000g of PVC and 11g of azobisisobutyronitrile, and react at 80°C for 12 hours to obtain the silicone polymer Modified PVC.
[0023] (3) 60 g of silicone polymer modified PVC obtained in step (2), 5 g of nano-calcium carbonate...
Embodiment 2
[0026] (1) Add 500 g of toluene, 250 g of deionized water and 50 g of 1 mol / L H in a 3 L clean three-neck flask 2 SO 4 Aqueous solution, under stirring at 40 ℃, began to drop 24.8g of methacryloxypropyltrimethoxysilane, 208g of methyl orthosilicate, 240g of dimethyldiethoxysilane, 360g of methylbenzene Dimethoxysilane, 204 g methyltrimethoxysilane, and 8.6 g tetramethyldivinyldisiloxane were added dropwise within 0.5 to 1 h, and the temperature was raised to 78 °C for 0.5 h. After washing the oil phase to neutrality and removing the solvent and low molecules under reduced pressure at 180°C / 20 mm Hg, 460 g of vinyl-terminated, methacryloxypropyl-containing organosilicon polymers were obtained Material.
[0027](2) Take 20 g of the vinyl-terminated, methacryloxypropyl-containing organosilicon polymer material obtained in (1), 1000 g of PVC and 0.51 g of azobisisoheptanonitrile, and react at 100°C for 8 h, obtain organosilicon polymer modified PVC.
[0028] (3) 80 g of organi...
Embodiment 3
[0031] (1) Add 1000 g of xylene, 400 g of deionized water and 58.8 g of 0.1 mol / L p-toluenesulfonic acid into a 3 L clean three-necked flask. 39.5g acryloxytrimethylsilane, 10g acryloxydisiloxane, 208g ethyl orthosilicate, 240g dimethyldiethoxysilane, 380g diphenyldimethoxysilane, 248 g of methyltriethoxysilane and 53.8g of dimethylvinylethoxysilane were dropped within 0.5 to 1 h, then reacted at 60 °C for 24 h, stood and separated, and the oil phase was washed until After neutralization, the solvent and low molecules were removed under reduced pressure at 180° C. / 20 mm Hg to obtain 460 g of acryloyloxy group-containing organosilicon polymer material.
[0032] (2) Take 100g of the acryloyloxy group-containing silicone polymer material obtained in (1), 1000g of PVC and 1.1 g of dimethyl azobisisobutyrate, and react at 120°C for 4 hours to obtain the silicone polymer Modified PVC.
[0033] (3) Mix 70 g of organosilicon polymer modified PVC obtained in step (2), 5 g of nano-cal...
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