Centro de Investigaciones en Catálisis, Escuela de Ingeniería Química, Universidad Industrial de Santander (UIS), A.A. 678, Bucaramanga, Colombia.
J Hazard Mater. 2012 Apr 15;211-212:172-81. doi: 10.1016/j.jhazmat.2011.08.076. Epub 2011 Sep 3.
Ag loaded TiO(2) was applied in the photocatalytic inactivation of Escherichia coli under ultraviolet (UV) and visible (Vis) light irradiations. Ag enhanced the TiO(2) photodisinfecting effect under Vis irradiation promoting the formation of singlet oxygen and hydroxyl radicals as identified by EPR analyses. Ag nanoparticles, determined on TEM analyses, undergo an oxidation process on the TiO(2)'s surface under UV or Vis irradiation as observed by XPS. In particular, UV pre-irradiation of the material totally diminished its photodisinfection activity under a subsequent Vis irradiation test. Under UV, photodegradation of dichloroacetic acid (DCA), attributed to photoproduced holes in TiO(2), was inhibited by the presence of Ag suggesting that oxidation of Ag(0) to Ag(+) and Ag(2+) is faster than the oxidative path of the TiO(2)'s holes on DCA molecules. Furthermore, photoassisted increased of Ag(+) concentration on TiO(2)'s surface enhances the bacteriostatic activity of the material in dark periods. Indeed, this latter dark contact of Ag(+)-TiO(2) and E. coli seems to induce recovering of the Vis light photoactivity promoted by the surface Ag photoactive species.
负载银的 TiO(2) 在紫外 (UV) 和可见 (Vis) 光照射下被应用于光催化灭活大肠杆菌。Ag 通过电子顺磁共振 (EPR) 分析促进了单线态氧和羟基自由基的形成,增强了 TiO(2) 在 Vis 光照射下的光消毒效果。TEM 分析确定的 Ag 纳米颗粒在 UV 或 Vis 照射下,在 TiO(2)表面发生氧化过程,XPS 观察到这一点。特别是,材料在 UV 预先照射后,在随后的 Vis 照射测试下,其光消毒活性完全消失。在 UV 下,归因于 TiO(2)中光生空穴的二氯乙酸 (DCA) 的光降解被 Ag 的存在抑制,表明 Ag(0)氧化为 Ag(+)和 Ag(2+)比 TiO(2)空穴对 DCA 分子的氧化途径更快。此外,TiO(2)表面上光辅助增加的 Ag(+)浓度增强了材料在黑暗期的抑菌活性。事实上,Ag(+)-TiO(2)和大肠杆菌的这种黑暗接触似乎诱导了表面 Ag 光活性物质促进的 Vis 光光活性的恢复。