A method for preparing functional microspheres based on polyvinyl alcohol macromonomer
A macromonomer, functional technology, applied in the field of functional polymer microsphere preparation, can solve the problems of limiting the application field of PVA microspheres, toxic glutaraldehyde residue, etc., and achieves simple and easy method, stable dispersion, and reaction conditions. mild effect
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Embodiment 1
[0013] (1) Synthesis of PVA macromonomer: Take 1.05g of amino acetal dimethyl acetal and 1.01g of triethylamine in a 100mL three-necked flask by mass, dilute with dichloromethane, and slowly add 0.905g dropwise at 0°C Acryloyl chloride, then reacted for 3 hours, the product was washed with saturated brine, separated, and the organic phase was rotary evaporated to obtain N-(2,2-dimethoxyethyl)acrylamide; then PVA178810g was taken by mass, dissolved in Hot water at 90°C was prepared into a solution with a mass fraction of 10%. After cooling to room temperature, pour it into a 250mL three-neck flask, add 0.5g of N-(2,2-dimethoxyethyl)acrylamide, stir well, and Add 3mL of concentrated hydrochloric acid dropwise to the separatory funnel, react at room temperature for 24h, and obtain the PVA macromer through dialysis and freeze-drying;
[0014] (2) Preparation of functional microspheres: get the PVA macromer synthesized by 5g step (1), 0.5gAMPS, take potassium persulfate as initiato...
Embodiment 2
[0016] (1) Synthesis of PVA macromonomer: Take 1.05g of amino acetal dimethyl acetal and 1.01g of triethylamine in a 100mL three-necked flask by mass, dilute with dichloromethane, and slowly add 0.905g dropwise at 0°C Acryloyl chloride, then reacted for 3 hours, the product was washed with saturated brine, separated, and the organic phase was rotary evaporated to obtain N-(2,2-dimethoxyethyl)acrylamide; then PVA178810g was taken by mass, dissolved in Hot water at 90°C was prepared into a solution with a mass fraction of 10%. After cooling to room temperature, pour it into a 250mL three-neck flask, add 0.5g of N-(2,2-dimethoxyethyl)acrylamide, stir well, and Add 3mL of concentrated hydrochloric acid dropwise to the separatory funnel, react at room temperature for 24h, and obtain the PVA macromer through dialysis and freeze-drying;
[0017] (2) Preparation of functional microspheres: get the PVA macromer synthesized by 5g step (1), 1.0gAMPS, take potassium persulfate as initiato...
Embodiment 3
[0019] (1) Synthesis of PVA macromonomer: Take 1.05g of amino acetal dimethyl acetal and 1.01g of triethylamine in a 100mL three-necked flask by mass, dilute with dichloromethane, and slowly add 0.905g dropwise at 0°C Acryloyl chloride, then reacted for 3 hours, the product was washed with saturated brine, separated, and the organic phase was rotary evaporated to obtain N-(2,2-dimethoxyethyl)acrylamide; then PVA178810g was taken by mass, dissolved in Hot water at 90°C was prepared into a solution with a mass fraction of 10%. After cooling to room temperature, pour it into a 250mL three-neck flask, add 0.5g of N-(2,2-dimethoxyethyl)acrylamide, stir well, and Add 3mL of concentrated hydrochloric acid dropwise to the separatory funnel, react at room temperature for 24h, and obtain the PVA macromer through dialysis and freeze-drying;
[0020] (2) Preparation of functional microspheres: get the PVA macromer synthesized by 5g step (1), 1.5gAMPS, take potassium persulfate as initiato...
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