Glycidyl capped polyether, and synthesis method and applications thereof
A technology of glycidyl sealing and synthesizing method, which can be applied in the direction of coating, etc., can solve the problems of unsatisfactory foam suppression and shrinkage performance of end-capped polyethers.
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Embodiment 1
[0022] In the reactor equipped with stirrer, reflux band water device, add 50g octane / decyl alcohol polyether (ethylene oxide EO / propylene oxide PO=5 / 0), 80g toluene and 10.6g50wt% sodium hydroxide Aqueous solution (the molar ratio of polyether and sodium hydroxide is 1:1), heated up to 110°C for reaction, the reaction time is 1-3h, while refluxing with water, until the water content in the system is lower than 0.5%, dropwise add 13.5 g (the molar weight is equivalent to that of polyether) epichlorohydrin, after the dropwise addition is completed, react at a constant temperature of 110° C. for 8 hours. Filter to remove solid impurities, distill under reduced pressure to remove the solvent, add 100ml of distilled water to wash, stir and stand still to separate layers, remove the water phase, vacuum dry and dehydrate to obtain a blocked polyether product.
Embodiment 2
[0024] In the reactor equipped with stirrer and distillation device, add 240g decanol polyether (EO / PO=8 / 0), 200g xylene and 22.8g sodium methylate (the molar ratio of polyether and sodium methylate is 1:1 ), heat up to 80°C for reaction, the reaction time is 2-3.5h, and distill methanol at the same time until no methanol is distilled out, add 75g (molar weight equivalent to 2 times that of polyether) epichlorohydrin dropwise, and heat up after the dropwise addition Reaction at 140°C for 13h. Remove solid impurities by filtration, remove the solvent by distillation under reduced pressure, add 400ml of distilled water to wash, stir and static layer, remove the water phase, vacuum dry and dehydrate to obtain the end-capped polyether product.
Embodiment 3
[0026] In the reactor that stirrer, distillation unit are equipped with, add 320g butanol polyether (EO / PO=3 / 6), 300g toluene and 120g50wt% sodium methylate alcohol solution (the mol ratio of polyether and sodium methylate is 1: 2), heat up to 100°C to react, the reaction time is 3-4.5h, and distill methanol at the same time until no methanol is distilled out, add 81.5g (the molar weight is equivalent to 1.5 times of polyether) epichlorohydrin dropwise, and the dropwise addition is completed Afterwards, the temperature was raised to 120° C. for 13 hours. Filter to remove solid impurities, distill under reduced pressure to remove the solvent, add 500ml of distilled water to wash, stir and stand still to separate layers, remove the water phase, vacuum dry and dehydrate to obtain a blocked polyether product.
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