Journal
ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 44, Issue 24, Pages 9488-9495Publisher
AMER CHEMICAL SOC
DOI: 10.1021/es1028475
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Funding
- National Science Foundation [CBET-0932872]
- Center for Biological and Environmental Nanotechnology (NSF) [EEC-0647452]
- Robert A. Welch Foundation [C-0627]
- Directorate For Engineering
- Div Of Chem, Bioeng, Env, & Transp Sys [0932872, 0933219] Funding Source: National Science Foundation
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A new strategy is described to immobilize photoactive C-60 aminofullerene on silica gel (3-(2-succinic anhydride)propyl functionalized silica), thus enabling facile separation of the photocatalyst for recycling and repeated use. An organic linker moiety containing an amide group was used to anchor C-60 aminofullerene to the functionalized silica support. The linker moiety prevents aqueous C-60 aggregation/agglomeration (shown by TEM images), resulting in a remarkable enhancement of photochemical O-1(2) production under visible light irradiation. With no loss in efficacy of O-1(2) production plus insignificant chemical modification of the amino C-60/silica photocatalyst after multiple cycling, the system offers a promising new visible-light-activated photocatalyst. Under visible-light irradiation, the amino C-60/silica photocatalyst is capable of effective and kinetically enhanced oxidation of Ranitidine and Cimetidine (pharmaceutical pollutants) and inactivation of MS-2 bacteriophage compared to aqueous solutions of the C-60 aminofullerene alone. Thus, this photocatalyst could enable water treatment in less developed areas by alleviating dependence on major infrastructure, including the need for electricity.
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