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Low-temperature curable surface cross-linking agent of super absorbent polymer and preparing method of low-temperature curable surface cross-linking agent of super absorbent polymer
Low-temperature curable surface cross-linking agent of super absorbent polymer and preparing method of low-temperature curable surface cross-linking agent of super absorbent polymer
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机译:高吸收性聚合物的低温固化性表面交联剂及高吸收性聚合物的低温固化性表面交联剂的制备方法
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摘要
Disclosed is a preparation method of a low-temperature curing surface crosslinking agent of a superabsorbent resin, which comprises: a first step of mixing polyhydric alcohol and a Lewis acid catalyst at 30-40°C; a second step of adding epichlorohydrin to the mixture of the first step, and making reaction at 60-90°C to obtain halohydrin ether; a third step of adding a quaternary ammonium salt to halohydrin ether obtained in the second step and make reaction at 50-60°C; a fourth step of adding a strongly alkaline aqueous solution to a resultant product of the reaction in the third step to make condensation reaction; a fifth step of dividing the reaction product obtained in the fourth step into a salt layer and a resin layer including epichlorohydrin by using a dry filter at 40-60°C; a sixth step of recovering and removing excess of epichlorohydrin from the resultant product obtained in the fifth step; and a seventh step of adding an alkali absorbent to the resultant product obtained in the sixth step to perform mixing at 65-80°C. The fourth step of making condensation reaction includes: an A step of adding to the reaction product obtained in the third step a strongly alkaline aqueous solution as much as one third of strongly alkaline aqueous solution necessary for reaction with halohydrin ether to remove a salt water layer; and a B step of adding to the reaction product obtained in the A step a strongly alkaline aqueous solution as much as two-thirds of a strongly alkaline aqueous solution necessary for reaction with halohydrin ether to perform a decompression and dehydration process, wherein a reaction temperature in the B step is controlled to increase relative to the reaction temperature of the A step.
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