کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1489091 992299 2013 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Photocatalytic mineralization of carboxylic acids over Fe-loaded ZnS nanoparticles
موضوعات مرتبط
مهندسی و علوم پایه مهندسی مواد سرامیک و کامپوزیت
پیش نمایش صفحه اول مقاله
Photocatalytic mineralization of carboxylic acids over Fe-loaded ZnS nanoparticles
چکیده انگلیسی

Zinc sulfide (ZnS) nanoparticles prepared by hydrothermal synthesis were subsequentially impregnated with different iron amounts (0.5−5.0 at%) to obtain Fe-loaded ZnS nanoparticles. Phase composition, crystallinity, crystal size, and morphology of 0.5–5.0 at% Fe-loaded ZnS nanoparticles were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDXS), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma (ICP). Specific surface area determined by the Brunauer, Emmett and Teller (BET) method was found to be in the range of 85–197 m2/g. The average particle size obtained from TEM analysis of pure ZnS and 2.0 at% Fe-loaded ZnS nanoparticles was 5–20 nm. The optical absorption properties of the samples measured by UV–vis diffuse reflectance spectroscopy (UV–vis DRS) clearly indicated the bathochromic shift upon loading ZnS with Fe. Photocatalytic activities of pure ZnS and Fe-loaded ZnS nanoparticles were examined by studying the mineralization of oxalic acid and formic acid under UVA illumination. It was found that 2.0 at% Fe-loaded ZnS sample exhibited the highest degradation activity possibly due to the presence of Fe in an optimum amount and the increases of surface area and light absorption in UVA region.

Figure optionsDownload as PowerPoint slideHighlights
► Fe-loaded ZnS nanoparticles were prepared by hydrothermal and impregnation methods.
► Physicochemical properties played a significant role on photocatalytic efficiency.
► All Fe-loaded ZnS samples showed higher photocatalytic activity than pure ZnS.
► Fast degradation of oxalic acid may be due to high hydroxyl radical present.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Materials Research Bulletin - Volume 48, Issue 4, April 2013, Pages 1668–1674
نویسندگان
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