Yang Yan, Meng Xiangjun, Xiao Zhenggang
School of Chemical Engineering, Nanjing University of Science and Technology Nanjing 210094 China
RSC Adv. 2018 Mar 8;8(18):9802-9811. doi: 10.1039/c7ra13264f. eCollection 2018 Mar 5.
A surface molecular imprinting polymer (MIP) based on silica (SiO/MIP) with excellent selective identification properties towards nitrocellulose (NC) was synthesized with methylacrylic acid as a functional monomer and NC as a template molecule, through simple polymerization. The functional groups of SiO/MIP were studied through Fourier transform infrared spectroscopy. The morphology, crystalline state and thermostability of SiO/MIP were investigated respectively by scanning electron microscopy, X-ray diffraction and thermogravimetric analysis. Binding capacity and selectivity studies of SiO/MIP for NC and its analogues were carried out through ultraviolet-visible spectrophotometry. The thermal analysis and study of crystalline states confirmed the successful imprinting of NC in the polymer networks. The optimized conditions were found to be a polymerization temperature of 45 °C and a functional monomer to cross-linking ratio of 1 : 3. The adsorption capacity of SiO/MIP was improved considerably compared with that of polymers prepared by traditional imprinting technology, with a maximum adsorption amount of 1.7 mg mg in 2 mg ml NC solution, compared with an adsorption capacity of about 0.5 mg mg for a traditional MIP. According to the selectivity study, more NC was adsorbed by SiO/MIP than its analogues; the best adsorption capacity of SiO/MIP for NC was approaching 5 times that for carboxymethyl cellulose (CMC). The results show that it would be possible to apply SiO/MIP for the detection of NC, to give improved sensitivity in security checking and improved contaminant adsorption.
以甲基丙烯酸为功能单体、硝化纤维素(NC)为模板分子,通过简单聚合反应合成了一种对硝化纤维素具有优异选择性识别性能的基于二氧化硅的表面分子印迹聚合物(SiO/MIP)。通过傅里叶变换红外光谱研究了SiO/MIP的官能团。分别利用扫描电子显微镜、X射线衍射和热重分析对SiO/MIP的形貌、晶态和热稳定性进行了研究。通过紫外可见分光光度法对SiO/MIP对NC及其类似物的结合能力和选择性进行了研究。热分析和晶态研究证实了NC在聚合物网络中的成功印迹。发现优化条件为聚合温度45℃,功能单体与交联剂的比例为1∶3。与传统印迹技术制备的聚合物相比,SiO/MIP的吸附容量有了显著提高,在2mg/ml的NC溶液中最大吸附量为1.7mg/mg,而传统分子印迹聚合物的吸附容量约为0.5mg/mg。根据选择性研究,SiO/MIP对NC的吸附量比对其类似物的吸附量多;SiO/MIP对NC的最佳吸附容量接近对羧甲基纤维素(CMC)的吸附容量的5倍。结果表明,SiO/MIP可用于检测NC,在安全检查中提高灵敏度并改善污染物吸附。