Zhang Haiyan, Shi Yunsheng, Xu Xiafan, Zhang Min, Ma Lin
School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, P. R. China.
ACS Omega. 2020 Apr 24;5(17):10068-10076. doi: 10.1021/acsomega.0c00610. eCollection 2020 May 5.
To reveal the structure and release properties of bentonite-alginate nanocomposites, bentonite of different amounts was incorporated into alginate by the sol-gel route. The structure of the composites was characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and thermogravimetric analysis and related to the swelling property of the matrix and the release of imidacloprid. Bentonite was subject to exfoliation into nanoplatelets and combined into the polymeric network within alginate hydrogel, exhibiting profound effects on the structure features and release properties of the composites. Bentonite was of good compatibility with alginate due to the hydrogen bonding and the electrostatic attraction between them. The polymer chains were found to intercalate into the interlayer gallery of the clay. The high specific area of the nanoplatelets of bentonite benefited the intimate contact with alginate and reduced the permeability of the composites. However, in the composites with clay content of more than 10%, the polymer was insufficient to accommodate the silicate sheets completely. The aggregation of the platelets destroyed the structure integrity of the composites, facilitating the diffusion of the pesticide. The release of imidacloprid was greatly retarded by incorporating into bentonite-alginate composites and dominated by Fickian diffusion depending on the permeability of the matrix. The time taken for 50% of the active ingredient to be released, , first increased and then decreased with increasing clay content in the composites, reaching a maximum around a weight percentage of 10%, at which the value for imidacloprid release was about 2.5 times that for the release from pure alginate formulation.
为揭示膨润土-海藻酸钠纳米复合材料的结构和释放性能,通过溶胶-凝胶法将不同量的膨润土掺入海藻酸钠中。采用傅里叶变换红外光谱、X射线衍射、扫描电子显微镜和热重分析对复合材料的结构进行表征,并将其与基质的溶胀性能和吡虫啉的释放情况相关联。膨润土可剥落成纳米片层并结合到海藻酸盐水凝胶的聚合物网络中,对复合材料的结构特征和释放性能产生深远影响。由于膨润土与海藻酸钠之间存在氢键和静电吸引作用,二者具有良好的相容性。发现聚合物链可插入粘土的层间通道。膨润土纳米片层的高比表面积有利于与海藻酸钠紧密接触并降低复合材料的渗透性。然而,在粘土含量超过10%的复合材料中,聚合物不足以完全容纳硅酸盐片层。片层的聚集破坏了复合材料的结构完整性,促进了农药的扩散。将吡虫啉掺入膨润土-海藻酸钠复合材料中可大大延缓其释放,且释放过程以菲克扩散为主,这取决于基质的渗透性。活性成分释放50%所需的时间(t_{50})随复合材料中粘土含量的增加先增加后减少,在重量百分比约为10%时达到最大值,此时吡虫啉释放的(t_{50})值约为从纯海藻酸钠制剂中释放时的2.5倍。