首页|期刊导航|南京工业大学学报(自然科学版)|聚合诱导分相制备聚丙烯酸@壳聚糖核壳乳液和微球的研究

聚合诱导分相制备聚丙烯酸@壳聚糖核壳乳液和微球的研究OACHSSCD

Study on polymerization-induced phase separation for the preparation of poly(acrylic acid)@CS core-shell emulations and microspheres

中文摘要英文摘要

本研究旨在构建一种基于微流控技术的聚合诱导分相体系,通过条件考察确定丙烯酸(AA)质量分数为10%、壳聚糖(CS)质量分数为0.5%~1.0%、N,N'-亚甲基双丙烯酰胺(MBA)质量分数为1%及紫外光源输出功率≥70%为最佳的组分比例及固化条件,实现核壳结构的PAA@CS微液滴与微球的可控制备.以AA、MBA、CS的水溶液为分散相,以含鲸蜡基聚乙二醇(EM-90)的液体石蜡为连续相,在同轴微流控装置中获得均一液滴,再经紫外辐照诱导聚合与相分离.系统考察AA质量分数、MBA质量分数、CS质量分数及紫外光源输出功率对液滴内核/外壳尺寸比(r/R)及分相行为的影响,并对固化后微球进行形貌与结构表征.在实验体系中,CS的加入是形成核壳结构的关键条件;在MBA质量分数为0~2%范围内,r/R随MBA含量呈非线性变化;AA质量分数增加,r/R显著减小;紫外光源输出功率低于40%不能诱导明显相分离.最佳条件下,未交联核壳液滴的平均粒径约为434 μm,交联后固体微球保持良好球形与完整的核壳结构,平均粒径为240 μm.微流控结合聚合诱导分相可实现PAA@CS核壳微液滴及微球的可控构筑,其中AA质量分数为10%、CS质量分数为0.5%~1.0%、MBA质量分数为1.0%的组分比例,与≥70%的紫外光固化强度共同调控内核生成与结构稳定性.本研究为功能化核壳微球的设计与应用提供了可行策略.

This study aims to construct a microfluidics-based polymerization-induced phase separation(PIPS)system.Through systematic investigation of experimental conditions,it is determined that the optimal component ratios and curing conditions are as follows:acrylic acid(AA)with a mass fraction of 10%,chitosan(CS)with a mass fraction of 0.5%~1.0%,N,N'-methylenebisacrylamide(MBA)with a mass fraction of 1.0%,and the output power of UV light source of ≥70%.These optimized conditions enable the controllable preparation of core-shell structured PAA@CS microdroplets and microspheres.An aqueous solution of AA,MBA,and CS was used as the dispersed phase,while liquid paraffin containing EM-90 served as the continuous phase.Uniform droplets were generated through a coaxial microfluidic device and subsequently subjected to UV irradiation to trigger polymerization and phase separation.The effects of the mass fractions of AA,MBA,and CS,together with UV intensity,on the core-to-shell radius ratio(r/R)and phase separation behavior were systematically investigated.The morphology and internal structure of the cured microspheres were further characterized.The results show that adding CS was essential for the formation of a core-shell structure.When the mass fraction of MBA was between 0 and 2%,r/R varied nonlinearly with MBA content.Increasing the AA content led to a significant decrease in r/R.When the output power of UV light source was below 40%,no obvious phase separation occurred.Under optimal conditions,the average particle size of uncrosslinked core-shell droplets is approximately 434 μm.After crosslinking,the solid microspheres maintain a well-defined spherical shape and intact core-shell structure,with an average particle size of 240 μmn.The combination of microfluidics and polymerization-induced phase separation enables the controllable fabrication of core-shell PAA@CS microdroplets and microspheres.Among the optimized conditions,the components ratios including AA(10%),CS(0.5%-1.0%),and MBA(1.0%),together with an UV curing intensity of ≥70%,jointly regulated the formation of the PAA core and the structural stability of the core-shell structure.This study provides a feasible strategy for the design and application of functional core-shell microspheres.

朱凯旋;李康;张锋;刘佳;张利雄

江苏科技大学苏州理工学院电气与信息工程学院,江苏张家港 215600南京工业大学材料化学工程全国重点实验室,江苏 南京 211800||南京工业大学化工学院,江苏南京 211800南京工业大学材料化学工程全国重点实验室,江苏 南京 211800||南京工业大学化工学院,江苏南京 211800南京工业大学药学院,江苏南京 211800南京工业大学材料化学工程全国重点实验室,江苏 南京 211800||南京工业大学化工学院,江苏南京 211800

化学化工

微流控紫外光固化聚合诱导分相核壳结构液滴功能微球相分行为调控

microfluidicsUV curingpolymerization-induced phase separationcore-shell microdropletsfunctional microspheresphase separation control

《南京工业大学学报(自然科学版)》 2026 (1)

89-97,106,10

材料化学工程全国重点实验室开放课题(SKL-MCE-24B08)

10.3969/j.issn.1671-7627.2026.01.009

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