Photocatalytic Degradation of Methylene Blue Dye with Green Zinc Oxide Doped with Nitrogen

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引用次数: 1

Abstract

The non-biodegradability of organic pollutants and their adverse effects on plant and living organisms makes their removal from the environment vital for the preservation of the ecosystem. In this study, Photocatalysis (one of the advanced oxidation processes) was employed for the removal of methylene blue dye (MBD). Phyto-enhanced synthesized Zinc oxide (G.S ZnO) were precipitated from an aqueous solution of zinc nitrate hexahydrate and Papaya leaf extracts. The precipitates were dried at 100 oC for 24 hours, and doped hydrothermally with nitrogen from Urea at different doping ratios (10%, 5% and 2%). Preliminary degradation of MBD with the different compositions of Photocatalyst revealed that 5% G.S N-ZnO had superior photocatalytic capabilities than pure ZnO, 10% G.S N-ZnO, 2% G.S N-ZnO. The effects of solution pH, 5% G.S N-ZnO dosage and initial solution concentration on MBD degradation were studied. An optimum percentage degradation of 83% and 97.5% were observed for pure ZnO and G.S. N-ZnO photocatalyst at a solution pH of 9.0, MB solution concentration of 10 mg/L and photocatalyst of dosage of 100 mg. Scanning Electron Microscope (SEM), X-ray Diffraction (XRD), Brunauer-Emmett-Teller (BET) and Fourier Transform Infrared Spectroscopy (FTIR) were used to study morphology, structural properties, surface area and pore volume, and functional groups of Pure ZnO and 5% G.S N-ZnO. FTIR spectra of the 5% G.S N-ZnO was in the range of 4000-500cm-1, and the ZnO group of G.S N-ZnO was at a low wavenumber. The BET result revealed the surface area of 5% G.S N-ZnO to be 113.3cm2/g which was five times that of pure ZnO. The BET result showed an increase in pore volume and diameter (2.118nm and 0.055cm3/g) of 5% G.S N-ZnO against that of pure ZnO (1.452 nm and 0.010 cm3/g). The shift of the XRD pattern between pure ZnO and 5% G.S N-ZnO affirms the presence of dopants in the crystalline structure of ZnO. The average crystallite sizes of pure ZnO and 5% G.S N-ZnO were 34.7nm and 24.8nm, respectively. The findings from this research revealed that the simultaneous use of green synthesis and doping could further improve the degradation of methylene blue dye compounds in industrial effluents and ultimately increase the efficiency of wastewater treatment processes/systems.
氮掺杂氧化锌光催化降解亚甲基蓝染料
有机污染物的不可生物降解性及其对植物和生物体的不利影响使得将其从环境中清除对于保护生态系统至关重要。本研究采用高级氧化工艺之一的光催化法脱除亚甲基蓝染料(MBD)。从六水硝酸锌和木瓜叶提取物的水溶液中沉淀植物增强合成氧化锌(G.S ZnO)。沉淀物在100℃下干燥24小时,并以不同掺杂比例(10%,5%和2%)的尿素氮进行水热掺杂。不同组成的光催化剂对MBD的初步降解表明,5% G.S N-ZnO的光催化性能优于纯ZnO、10% G.S N-ZnO和2% G.S N-ZnO。研究了溶液pH、5% G.S N-ZnO投加量和初始溶液浓度对MBD降解的影响。当溶液pH为9.0、MB浓度为10 mg/L、光催化剂用量为100 mg时,纯ZnO和G.S. N-ZnO光催化剂的最佳降解率分别为83%和97.5%。采用扫描电镜(SEM)、x射线衍射(XRD)、布鲁诺尔-埃米特-泰勒光谱(BET)和傅里叶变换红外光谱(FTIR)研究了纯ZnO和5% G.S N-ZnO的形貌、结构性质、比表面积、孔体积和官能团。5% G.S N-ZnO的FTIR光谱在4000 ~ 500cm-1范围内,其中G.S N-ZnO的ZnO基团处于低波数。BET结果显示,5% G.S N-ZnO的比表面积为113.3cm2/g,是纯ZnO的5倍。BET结果表明,5% g . s - N-ZnO的孔隙体积和孔径(2.118nm和0.055cm3/g)比纯ZnO (1.452 nm和0.010 cm3/g)增加。XRD谱图在纯ZnO和5% G.S N-ZnO之间的变化证实了ZnO晶体结构中掺杂物的存在。纯ZnO和5% G.S N-ZnO的平均晶粒尺寸分别为34.7nm和24.8nm。本研究结果表明,同时使用绿色合成和掺杂可以进一步改善工业废水中亚甲基蓝染料化合物的降解,最终提高废水处理工艺/系统的效率。
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