scholarly journals Degradation Kinetics of Methyl Orange Dye in Water Using Trimetallic Fe/Cu/Ag Nanoparticles

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 428
Author(s):  
Masaku Kgatle ◽  
Keneiloe Sikhwivhilu ◽  
Gebhu Ndlovu ◽  
Nosipho Moloto

The release of azo dye contaminants from textile industries into the environment is an issue of major concern. Nanoscale zerovalent iron (nZVI) has been extensively studied in the degradation of azo dye pollutants such as methyl orange (MO). In this study, iron was coupled with copper and silver to make trimetallic Fe/Cu/Ag nanoparticles, in order to enhance the degradation of MO and increase reactivity of the catalyst by delaying the rate of oxidation of iron. The synthesis of the trimetallic nanoparticles (Fe/Cu/Ag) was carried out using the sodium borohydride reduction method. The characterization of the particles was performed using XRD, XPS, EDX, and TEM. The analyses confirmed the successful synthesis of the nanoparticles; the TEM images also showed the desired structures and geometry of the nanoscale zerovalent iron particles. The assessment of the nanoparticles in the degradation of methyl orange showed a notable degradation within few minutes into the reaction. The effect of parameters such as nanoparticle dosage, initial MO concentration, and the solution pH on the degradation of MO using the nanoparticles was investigated. Methyl orange degradation efficiency reached 100% within 1 min into the reaction at a low pH, with lower initial MO concentration and higher nanoparticle dosage. The degradation rate of MO using the nanoparticles followed pseudo first-order kinetics and was greatly influenced by the studied parameters. Additionally, LC-MS technique confirmed the degradation of MO within 1 min and that the degradation occurs through the splitting of the azo bond. The Fe/Cu/Ag trimetallic nanoparticles have proven to be an appropriate and efficient alternative for the treatment of dye wastewater.

Author(s):  
J. J. Lian ◽  
M. Yang ◽  
H. L. Wang ◽  
Y. Zhong ◽  
B. Chen ◽  
...  

Abstract The overall goal of this study is to investigate the effect of sulfidated nanoscale zerovalent iron (S-nZVI) on the removal of hexavalent molybdate (MoO42-) under different aquatic chemistry conditions. Surface analysis suggests that Mo(VI) is removed mainly by adsorption and co-precipitation onto the surface of S-nZVI and a small amount of Mo(VI) can be reduced to Mo(V) species. The results of batch tests show that Mo(VI) removal by S-nZVI are well described with the pseudo-second order adsorption model. The removal rate increases with a decrease in solution pH (4.0–9.0) and significantly affected by the S/Fe ratio of S-nZVI with the optimal S/Fe ratio of 0.5. The presence of anions WO42- or CrO42- can reduce the Mo(VI) removal, which is likely due to that they compete for adsorption sites on the solid surfaces. The divalent cations Ni2+, Cu2+ and Co2+ also inhibit the removal of Mo(VI) whereas Zn2+, Ca2+ and Mg2+ enhance it. After aged for 35 d in water, S-nZVI still exhibits high reactivity towards Mo(VI) removal (57.39%). The study demonstrate that S-nZVI can be used as an environmentally friendly material for effectively removing Mo(VI) from contaminated water.


2007 ◽  
Vol 314 (1) ◽  
pp. 89-97 ◽  
Author(s):  
Hung-Yee Shu ◽  
Ming-Chin Chang ◽  
Hsing-Hung Yu ◽  
Wang-Hung Chen

2019 ◽  
Author(s):  
Chem Int

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jien Ye ◽  
Yi Wang ◽  
Qiao Xu ◽  
Hanxin Wu ◽  
Jianhao Tong ◽  
...  

AbstractPassivation of nanoscale zerovalent iron hinders its efficiency in water treatment, and loading another catalytic metal has been found to improve the efficiency significantly. In this study, Cu/Fe bimetallic nanoparticles were prepared by liquid-phase chemical reduction for removal of hexavalent chromium (Cr(VI)) from wastewater. Synthesized bimetallic nanoparticles were characterized by transmission electron microscopy, Brunauer–Emmet–Teller isotherm, and X-ray diffraction. The results showed that Cu loading can significantly enhance the removal efficiency of Cr(VI) by 29.3% to 84.0%, and the optimal Cu loading rate was 3% (wt%). The removal efficiency decreased with increasing initial pH and Cr(VI) concentration. The removal of Cr(VI) was better fitted by pseudo-second-order model than pseudo-first-order model. Thermodynamic analysis revealed that the Cr(VI) removal was spontaneous and endothermic, and the increase of reaction temperature facilitated the process. X-ray photoelectron spectroscopy (XPS) analysis indicated that Cr(VI) was completely reduced to Cr(III) and precipitated on the particle surface as hydroxylated Cr(OH)3 and CrxFe1−x(OH)3 coprecipitation. Our work could be beneficial for the application of iron-based nanomaterials in remediation of wastewater.


Optik ◽  
2021 ◽  
Vol 231 ◽  
pp. 166431
Author(s):  
Thuy Van Nguyen ◽  
Duc Chinh Vu ◽  
Van Hai Pham ◽  
Thanh Binh Pham ◽  
Van Hoi Pham ◽  
...  

2014 ◽  
Vol 280 ◽  
pp. 504-513 ◽  
Author(s):  
Yiming Su ◽  
Adeyemi S. Adeleye ◽  
Xuefei Zhou ◽  
Chaomeng Dai ◽  
Weixian Zhang ◽  
...  

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