Wu Yinqiu, Zhang Yang, Wang Kailun, Luo Zili, Xue Zhiyu, Gao Hongxin, Cao Zheng, Cheng Junfeng, Liu Chunlin, Zhang Lei
Jiangsu Key Laboratory of Environmentally Friendly Polymeric Materials, School of Materials Science and Engineering, Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Changzhou University, Changzhou 213164, Jiangsu, P. R. China.
Changzhou University Huaide College, Jingjiang 214500, P. R. China.
ACS Omega. 2021 Feb 15;6(8):5764-5774. doi: 10.1021/acsomega.0c06181. eCollection 2021 Mar 2.
This study aimed to reveal the interaction between self-assembled multilayers and dye molecules in the environment, which is closely related to the multilayers' stable performance and service life. In this work, the pH-responsive poly (-isopropylacrylamide--2-(dimethylamino) ethyl methacrylate) microgels were prepared by free-radical copolymerization and self-assembled with sodium alginate (SA) into multilayers by the layer-by-layer deposition method. Quartz crystal microbalance (QCM) and atomic force microscopy (AFM) results confirmed the construction of multilayers and the absorbed mass, resulting in a decrease in the frequency shift of the QCM sensor and the deposition of microgel particles on its surface. The interaction between the self-assembled SA/microgel multilayers and anionic dyes in the aqueous solution was further investigated by QCM, and it was found that the electrostatic attraction between dyes and microgels deposited on the QCM sensor surface was much larger than that of the microgels with SA in multilayers, leading to the release of the microgels from the self-assembled structure and a mass loss ratio of 27.6%. AFM observation of the multilayer morphology exposed to dyes showed that 29% of the microgels was peeled off, and the corresponding microgel imprints were generated on the surface. In contrast, the shape and size of the remaining self-assembled microgel particles did not change.
本研究旨在揭示自组装多层膜与环境中染料分子之间的相互作用,这与多层膜的稳定性能和使用寿命密切相关。在本工作中,通过自由基共聚制备了pH响应性聚(-异丙基丙烯酰胺-甲基丙烯酸2-(二甲氨基)乙酯)微凝胶,并通过层层沉积法与海藻酸钠(SA)自组装成多层膜。石英晶体微天平(QCM)和原子力显微镜(AFM)结果证实了多层膜的构建和吸附质量,导致QCM传感器的频率偏移减小以及微凝胶颗粒在其表面的沉积。通过QCM进一步研究了自组装SA/微凝胶多层膜与水溶液中阴离子染料之间的相互作用,发现染料与沉积在QCM传感器表面的微凝胶之间的静电吸引力远大于多层膜中微凝胶与SA之间的静电吸引力,导致微凝胶从自组装结构中释放,质量损失率为27.6%。对暴露于染料的多层膜形态进行AFM观察表明,29%的微凝胶被剥离,并在表面产生了相应的微凝胶印记。相比之下,剩余自组装微凝胶颗粒的形状和尺寸没有变化。