Agorku E S, Mittal H, Mamba B B, Pandey A C, Mishra A K
Department of Applied Chemistry, University of Johannesburg, South Africa.
Nanotechnology and Application Centre, University of Allahabad, India.
Int J Biol Macromol. 2014 Sep;70:143-9. doi: 10.1016/j.ijbiomac.2014.06.037. Epub 2014 Jun 28.
This research paper reports the photocatalytic properties of Zn-SiO2-Eu3+ and sodium alginate (Alg) based nanocomposites for the degradation of indigo carmine dye. Initially, Eu3+ doped ZnS-SiO2 nanophorphor was synthesized and after that it was incorporated within the grafted crosslinked polymer matrix of Alg with acrylamide-co-acrylic acid in different concentrations. Synthesized materials were characterized using XRD, Raman spectroscopy, FTIR, SEM/EDX, TEM and UV-vis diffuse reflectance spectroscopy. XRD and TEM analyses confirmed the formation of nanoparticles as well as the uniform distribution of the nanoparticles within the polymer matrix. The UV-vis and UV-vis DRS spectral analysis indicated that Eu3+ doping causes a red-shift in the absorption band, resulting in the reduction in band gaps. The synergic effect of ZnS and Eu3+ in the SiO2 evidenced the photocatalytic performance of the catalyst. Alg-cl-poly(AAM-co-MAA)/ZnS-SiO2-Eu3+ nanocomposites were found to be very effective for the degradation of indigo carmine under visible light. Highest photocatalytic performance (93.4%) was shown by the nanocomposite with the 20% concentration of the nanoparticle after 5h. The photocatalytic activity was mainly attributed to the intense light absorption in the visible region and narrow band gap energy.
本研究论文报道了基于Zn-SiO₂-Eu³⁺和海藻酸钠(Alg)的纳米复合材料对靛蓝胭脂红染料降解的光催化性能。最初,合成了Eu³⁺掺杂的ZnS-SiO₂纳米磷光体,之后将其以不同浓度掺入Alg与丙烯酰胺-丙烯酸的接枝交联聚合物基质中。使用X射线衍射(XRD)、拉曼光谱、傅里叶变换红外光谱(FTIR)、扫描电子显微镜/能谱仪(SEM/EDX)、透射电子显微镜(TEM)和紫外-可见漫反射光谱对合成材料进行了表征。XRD和TEM分析证实了纳米颗粒的形成以及纳米颗粒在聚合物基质中的均匀分布。紫外-可见光谱和紫外-可见漫反射光谱分析表明,Eu³⁺掺杂导致吸收带发生红移,从而使带隙减小。ZnS和Eu³⁺在SiO₂中的协同作用证明了催化剂的光催化性能。发现Alg-cl-聚(丙烯酰胺-共-甲基丙烯酸)/ZnS-SiO₂-Eu³⁺纳米复合材料在可见光下对靛蓝胭脂红的降解非常有效。5小时后,纳米颗粒浓度为20%的纳米复合材料表现出最高的光催化性能(93.4%)。光催化活性主要归因于在可见光区域的强烈光吸收和窄带隙能量。