目的:制备双酚A环氧衍生物的分子印迹聚合物。方法采用沉淀聚合法,以双酚A(bisphenol A, BPA)和双酚A二环氧甘油(bisphenol A diglycidyl ether, BADGE)为双模板分子,α-甲基丙烯酸(methacrylic acid, MAA)为功能单体,三羟甲基丙烷三甲基丙烯酸酯(trimethylolpropane trim ethacrylate, TRIM)为交联剂,偶氮二异丁腈(azodiisobutyronitrile, AIBN)为引发剂,合成了一种高选择性的分子印迹聚合物,运用扫描电镜、红外光谱分析等手段对其形貌、物理特征进行了表征,同时进行了聚合物的静态吸附与动态吸附性能研究。结果合成的分子印迹聚合物(molecularly imprinted polymers, MIPs)对10种化合物的最大平衡吸附量为18.12~27.00 mg/g,对10种化合物的吸附略有区别,但差异不大,而非印迹聚合物(non-imprinted polymers, NIPs)则对10种化合物的吸附量为7.10~10.73 mg/g,说明NIPs吸附是由于存在物理吸附。结论10种目标化合物在MIPs上均有吸附,能够应用于分子印迹-固相萃取-高效液相色谱检测方法的建立。
Objective To synthesize the molecular imprinted polymers (MIPs) of bisphenol A epoxy derivatives. MethodsThe molecular imprinted polymers (MIPs) was synthesized by polymerization for 24 h using bisphenol A and bisphenol A diglycidyl ether as double templates,α-methacrylic acid (MAA) as monomer, trimethylolpropane trim ethacrylate (TRIM) as cross-linker and 2,2-zaobisisobutyronitrile (AIBN) as initiator. The polymers were characterized by IR spectra and scanning electron microscope and the adsorbent capacity and selectivity were also evaluated.Results The max adsorption capacity (Qmax) of MIPs was between 18.12~27.00 mg/g and the max adsorption capacity (Qmax) of NIPs was between 7.10~10.73 mg/g. The prepared MIPs showed a little different absorption abilities to 10 bisphenol A epoxy derivatives.Conclusion The prepared MIPs showed a better absorption of 10 bisphenol A epoxy derivatives and thus could be used to develop a method for the simultaneous determination of bisphenol