Gao Shuang, Jiang Jing-Yu, Liu Yan-Yan, Fu Ying, Zhao Li-Xia, Li Chun-Yan, Ye Fei
College of Science, Northeast Agricultural University, Harbin 150030, China.
College of Resources and Environment, Northeast Agricultural University, Harbin 150030, China.
Polymers (Basel). 2019 Aug 25;11(9):1396. doi: 10.3390/polym11091396.
The herbicide diuron is hardly soluble in water and most organic solvents and is usually made into a wettable powder or mixed with soil when used, which causes environmental risk and a reduction in herbicidal efficacy. In this study, the physicochemical properties were changed by using -cyclodextrin (-CD) to encapsulate diuron to form an inclusion complex. Some key technologies, including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and nuclear magnetic resonance (H NMR), were used to characterize the inclusion complex. The stoichiometry of the inclusion complex was determined by recording the H NMR spectrum or by using a diagram of inclusion ratios. A phase solubility study proved that the formed inclusion complex exhibited higher water solubility. Thermogravimetric analysis (TGA) demonstrated that the formed inclusion complex exhibited better thermal stability. Biological activity studies indicated that the herbicidal activity, in terms of herbicide removal, of the formed inclusion complex was higher than that of the original diuron. In general, the formation of the inclusion complex could reduce the environmental damage caused by diuron and enhance its herbicidal activity, providing an environmentally friendly method for using diuron.
除草剂敌草隆几乎不溶于水和大多数有机溶剂,使用时通常制成可湿性粉剂或与土壤混合,这会导致环境风险并降低除草效果。在本研究中,通过使用β-环糊精(β-CD)包封敌草隆以形成包合物来改变其物理化学性质。采用了一些关键技术,包括X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、差示扫描量热法(DSC)和核磁共振(H NMR)来表征该包合物。通过记录H NMR光谱或使用包合比图来确定包合物的化学计量比。相溶解度研究证明,形成的包合物具有更高的水溶性。热重分析(TGA)表明,形成的包合物具有更好的热稳定性。生物活性研究表明,就除草效果而言,形成的包合物的除草活性高于原始敌草隆。总体而言,包合物的形成可以减少敌草隆对环境的破坏并增强其除草活性,为敌草隆的使用提供了一种环保方法。