Abstract
A surface molecular imprinting polymer (MIP) based on silica (SiO(2)/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 in situ polymerization. The functional groups of SiO(2)/MIP were studied through Fourier transform infrared spectroscopy. The morphology, crystalline state and thermostability of SiO(2)/MIP were investigated respectively by scanning electron microscopy, X-ray diffraction and thermogravimetric analysis. Binding capacity and selectivity studies of SiO(2)/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(2)/MIP was improved considerably compared with that of polymers prepared by traditional imprinting technology, with a maximum adsorption amount of 1.7 mg mg(-1) in 2 mg ml(-1) NC solution, compared with an adsorption capacity of about 0.5 mg mg(-1) for a traditional MIP. According to the selectivity study, more NC was adsorbed by SiO(2)/MIP than its analogues; the best adsorption capacity of SiO(2)/MIP for NC was approaching 5 times that for carboxymethyl cellulose (CMC). The results show that it would be possible to apply SiO(2)/MIP for the detection of NC, to give improved sensitivity in security checking and improved contaminant adsorption.