scholarly journals Photochemical Oxidation Process of Copper from Electroplating Wastewater: Process Performance and Kinetic Study

Processes ◽  
2020 ◽  
Vol 8 (10) ◽  
pp. 1276
Author(s):  
Aji Prasetyaningrum ◽  
Teguh Riyanto ◽  
Mohamad Djaeni ◽  
Widayat Widayat

An investigation of the process of ozone combined with ultraviolet radiation has been carried out in order to establish the kinetics for photochemical oxidation of copper (Cu) from electroplating wastewater. The effects of operating parameters, including initial Cu concentration, ozone dosage, UV irradiation intensity, and pH value on the photochemical oxidation of Cu have been studied comprehensively. The Cu concentration during the reaction was identified using atomic absorption spectroscopy (AAS) method. The solid product was analyzed using X-ray diffraction (XRD) and scanning electron microscope–energy-dispersive X-ray (SEM–EDX) methods. It was found that the UV-Ozone process has high performance on Cu removal compared to UV and Ozone processes due to the high production rate of HO• radicals. It was also found that the solid product from the UV-Ozone process was CuO monoclinic crystal phase. The initial Cu concentration, ozone dosage, and pH value were significantly affected the Cu removal efficiency. On the other hand, the UV irradiation intensity was not significant; however, it has responsibility in promoting the ozone photolysis. The kinetics model for the photochemical oxidation of Cu was established following the first-order kinetic model. Furthermore, the reaction mechanism was also developed.

2017 ◽  
Vol 8 (3) ◽  
pp. 350-359 ◽  
Author(s):  
Danyang Yin ◽  
Zhengwen Xu ◽  
Jing Shi ◽  
Lili Shen ◽  
Zexiang He

Abstract In this study, schorl was used as an effective adsorbent for ciprofloxacin removal from wastewater. The adsorption performance, mechanism and effect of metal ion on sorption were investigated. Adsorption capacity reached a maximum (8.49 mg/g) when the pH value was 5.5. The pseudo-second-order kinetic model and Freundlich model could better describe the experimental data. The negative ΔH (–22.96 KJ/mol) value showed that the adsorption process was exothermic. The results also indicated physical adsorption existed on the adsorption process, which was in agreement with the analysis of X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy. The desorption rate could reach 94%, which suggested that schorl had a good desorption and regeneration performance. Coexisting ions, such as Cu2+ and Al3+, could obviously inhibit adsorption, and the inhibition from Al3+ was significantly higher than that from Cu2+. However, the additional Zn2+ could slightly promote the adsorption.


Coatings ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 824
Author(s):  
Li-Yuan Zhang ◽  
Jia You ◽  
Qian-Wen Li ◽  
Zhi-Hong Dong ◽  
Ya-Jie Zhong ◽  
...  

F–TiO2 was prepared by a simple precipitation method using titanium sulfate as the titanium source, hydrogen fluoride as the fluorine source and ammonia as the precipitant. CdS/F–TiO2 composites were prepared by hydrothermal synthesis of CdS and F–TiO2. The surface morphology, crystal phase composition, ultraviolet absorption band, fluorescence intensity, element composition, valence state, specific surface and pore structure of the samples were characterized by using field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), ultraviolet visible absorption spectrum (UV-Vis-Abs), Molecular fluorescence spectrophotometer (PL) and X-Ray photoelectron spectroscopy (XPS) and Surface area analyzer (BET), respectively. The effects of the dosage of the photocatalyst, pH value, the concentration of methyl orange and the addition of H2O2 on the photocatalytic performance were investigated with methyl orange solution as the target degradation product. The results showed the optimum condition for photodegradation of methyl orange by 1% CdS/F–TiO2 is that the pH value, the solid-liquid ratio, the concentration of methyl orange and the dosage of H2O2 is 2, 2 g/L, 10 mg/L and 3%, respectively. Under the same conditions, the degradation rate of methyl orange by 1% CdS/F–TiO2 was 93.36% when 300 W metal halide lamp was irradiated for 20 minutes, which was significantly higher than that of F–TiO2. CdS has a significant effect on the morphology, crystallinity, grain size and the compound probability of electrons and holes after the F–TiO2 modification. The composite causes a significant red shift at the edge of the F–TiO2 light absorption band. The photocatalytic degradation of methyl orange by 1% CdS/F–TiO2 follows the Langmuir-Hinshelwood first-order kinetic model.


2017 ◽  
Vol 4 (12) ◽  
pp. 170834 ◽  
Author(s):  
M. Nageeb Rashed ◽  
M. A. Eltaher ◽  
A. N. A. Abdou

Nanocomposite TiO 2 /ASS (TiO 2 nanoparticle coated sewage sludge-based activated carbon) was synthesized by the sol-gel method. The changes in surface properties of the TiO 2 /ASS nanocomposite were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-ray fluorescence. The prepared TiO 2 /ASS nanocomposite was applied for simultaneous removal of methyl orange dye (MO) and Cd 2+ from bi-pollutant solution. The factors influencing photocatalysis (TiO 2  : ASS ratios, initial pollutant concentrations, solution pH, nanocomposite dosage and UV irradiation time) were investigated. The results revealed that high removal efficiency of methyl orange dye (MO) and Cd 2+ from bi-pollutant solution was achieved with TiO 2 /ASS at a ratio (1 : 2). The obtained results revealed that degradation of MO dye on the TiO 2 /ASS nanocomposite was facilitated by surface adsorption and photocatalytic processes. The coupled photocatalysis and adsorption shown by TiO 2 /ASS nanocomposite resulted in faster and higher degradation of MO as compared to MO removal by ASS adsorbent. The removal efficiency of MO by ASS adsorbent and TiO 2 /ASS (1 : 2) nanocomposite at optimum pH value 7 were 74.14 and 94.28%, respectively, while for Cd 2+ it was more than 90%. The experimental results fitted well with the second-order kinetic reaction.


2017 ◽  
Vol 76 (8) ◽  
pp. 2106-2119 ◽  
Author(s):  
X. D. Ji ◽  
Y. Y. Ma ◽  
S. H. Peng ◽  
Y. Y. Gong ◽  
F. Zhang

In this study, zeolites were synthesized from low-calcium (LCZ) and high-calcium (HCZ) fly ash, respectively. Subsequently, the zeolites were tested for their removal effectiveness for four aqueous cations, namely, Zn2+, Cu2+, Cd2+, and Pb2+, as a function of contact time, pH value, adsorbent dosage, and initial concentration of heavy metals. Both zeolites were characterized by X-ray diffraction, X-ray fluorescence spectrometry, scanning electron microscopy, specific surface area, and cation exchange capacity. The results show that HCZ mainly consists of an unnamed zeolite (Na6[AlSiO4]6·4H2O), whereas LCZ mainly consists of faujasite-type zeolite. The optimum sorption conditions were pH = 6.0; adsorbent dosage = 1.0 g·L−1; temperature = 25 °C; contact time = 100 min; and initial heavy metal concentration = 100 mg·L−1. The sorption kinetics of the four aqueous cations on both LCZ and HCZ followed the pseudo-second-order kinetic model, and the sorption isotherm data fitted well with the Langmuir isotherm model. For LCZ, the maximum adsorption capacities of Zn2+, Cu2+, Cd2+, and Pb2+ were 155.76, 197.86, 123.76, and 186.22 mg·g−1, respectively. For HCZ, the values were 154.08, 183.15, 118.91, and 191.94 mg·g−1, respectively. The zeolites were regenerated by NaCl solution (1 mol·L−1) and showed high removal efficiency. In conclusion, zeolites produced by fly ash are promising materials for removing Zn2+, Cu2+, Cd2+, and Pb2+ from wastewater.


2018 ◽  
Vol 34 (12) ◽  
pp. 842-859 ◽  
Author(s):  
Asghar Khodkar ◽  
Seyed Mostafa Khezri ◽  
Alireza Pendashteh ◽  
Shahrzad Khoramnejadian ◽  
Leila Mamani

In this study, a new magnetic α-Fe2O3@MIL-101(Cr)@TiO2 photocatalyst was successfully synthesized. The material synthesized had been fully characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, vibrating sample magnetometry, transmission electron microscopy, and Brunauer–Emmett–Teller isotherm methods. The X-ray diffraction analysis corroborates that nanoparticles are polycrystalline with rhombohedral and tetragonal crystal structures for Fe2O3 and TiO2, respectively. In addition, the photocatalytic degradation of the herbicide paraquat in the presence of α-Fe2O3@MIL-101(Cr)@TiO2 under ultraviolet (UV) irradiation was studied. The effect of experimental parameters such as the initial concentration of catalyst, the pH, and the initial paraquat was investigated. The optimal conditions were achieved for concentration of catalyst 0.2 g L−1, pH 7, and concentration of paraquat 20 mg L−1. The photocatalytic degradation efficiency was 88.39% after 15 min with α-Fe2O3@MIL-101(Cr)@TiO2 under UV irradiation. The pseudo-second-order kinetic model for photocatalytic degradation of paraquat was obtained. The catalysts could be recovered and reused without any loss of efficiency for five times in the consequent reactions. To the best of our knowledge, this is the first report on the photocatalytic degradation of paraquat using new α-Fe2O3@MIL-101(Cr)@TiO2 photocatalyst under UV irradiation condition.


Author(s):  
E. C. Buck ◽  
N. L. Dietz ◽  
J. K. Bates

Operations at former weapons processing facilities in the U. S. have resulted in a large volume of radionuclidecontaminated soils and residues. In an effort to improve remediation strategies and meet environmental regulations, radionuclide-bearing particles in contaminant soils from Fernald in Ohio and the Rocky Flats Plant (RFP) in Colorado have been characterized by electron microscopy. The object of these studies was to determine the form of the contaminant radionuclide, so that it properties could be established [1]. Physical separation and radiochemical analysis determined that uranium contamination at Fernald was not present exclusively in any one size/density fraction [2]. The uranium-contamination resulted from aqueous and solid product spills, air-borne dust particles, and from the operation of an incinerator on site. At RFP the contamination was from the incineration of Pu-bearing materials. Further analysis by x-ray absorption spectroscopy indicated that the majority of the uranium was in the 6+ oxidation state [3].


2020 ◽  
Vol 3 (3) ◽  
Author(s):  
Jothi M ◽  
Sowmiya K

Nickel Oxide (NiO) is an important transition metal oxide with cubic lattice structure. NiO is thermally stable that is suitable for tremendous applications in the field of optic, ceramic,glass, electro-chromic coatings, plastics, textiles, nanowires, nanofibers, electronics,energy technology, bio-medicine, magnetism and so on. In this present study, NiO nanoparticles were successfully synthesized by sol-gel technique. Nano-sols were prepared by dissolving Nickel-Chloride [NiCl2.6H2O] in NaOH solvent and were converted into nano structured gel on precipitation. A systematic change in preparation parameters like calcination temperature, time, pH value has been noticed in order to predict the influence on crystallite size. Then the prepared samples were characterized by the X-ray Diffraction Spectroscopic (XRD), UV-VIS Spectroscopy, Fourier Transform Infra-Red Spectroscopy (FTIR), Energy Dispersive X-ray Spectroscopy (EDX), Scanning Electron Microscopy (SEM) and Particle Size Analyzer (PSA). From XRD, the average crystalline-size has been calculated by Debye-Scherrer Equation and it was found to be 12.17 nm and the band gap energy of Nickel oxide (NiO) from UV studies reveals around 3.85 eV. Further, EDX and FTIR studies, confirm the presences of NiO nanoparticles. The SEM study exhibits the spherical like morphology of Nickel oxide (NiO). Further from PSA, the mean value of NiO nanoparticles has been determined.


2016 ◽  
pp. 565-570
Author(s):  
Huang Qin ◽  
Zhu Si-ming ◽  
Zeng Di ◽  
Yu Shu-juan

Sugar beet pulp (SBP) was used as low value adsorbent for the removal of calcium from hard water. Batch experiments were conducted to determine the factors affecting adsorption of the process such as pH value and Ca concentration. The adsorption equilibrium of Ca2+ by the SBP is reached after 100min and a pseudo second-order kinetic model can describe the adsorption process. The initial concentrations of Ca varied from 927 to 1127mgCa2+/L. A dose of 30g/L sugar beet pulp was sufficient for the optimum removal of calcium. The overall uptake of Ca ions by sugar beet pulp has its maximum at pH=8. The adsorption equilibrium data fitted well with the Langmuir adsorption isotherm equation.


2020 ◽  
Vol 16 (7) ◽  
pp. 880-892
Author(s):  
Şerife Parlayıcı ◽  
Kübra Tuna Sezer ◽  
Erol Pehlivan

Background: In this work, Cr (VI) adsorption on nano-ZrO2๏TiO2 impregnated orange wood sawdust (Zr๏Ti/OWS) and nano-ZrO2๏TiO2 impregnated peach stone shell (Zr๏Ti/PSS) was investigated by applying different adsorption parameters such as Cr (VI) concentrations, contact time, adsorbent dose, and pH for all adsorbents. Methods: The adsorbents were characterized by SEM and FT-IR. The equilibrium status was achieved after 120 min of contact time and optimum pH value around 2 were determined for Cr (VI) adsorption. Adsorption data in the equilibrium is well-assembled by the Langmuir model during the adsorption process. Results: Langmuir isotherm model showed a maximum adsorption value of OWS: 21.65 mg/g and Zr๏Ti/OWS: 27.25 mg/g. The same isotherm displayed a maximum adsorption value of PSS: 17.64 mg/g, and Zr๏Ti/PSS: 31.15 mg/g. Pseudo-second-order kinetic models (R2=0.99) were found to be the best models for describing the Cr (VI) adsorption reactions. Conclusıon: Thermodynamic parameters such as changes in ΔG°, ΔH°, and ΔS° have been estimated, and the process was found to be spontaneous.


2021 ◽  
Vol 11 (7) ◽  
Author(s):  
Sabarish Radoor ◽  
Jasila Karayil ◽  
Aswathy Jayakumar ◽  
Jyotishkumar Parameswaranpillai ◽  
Suchart Siengchin

AbstractIn the present work, we have developed a mesoporous silicalite-1 using CMC as a template for the removal of MB from aqueous solution. The synthesized silicalite-1 were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Energy-dispersive X-ray spectroscopy (EDAX) and N2 adsorption–desorption isotherm (BET). XRD and FT-IR analysis confirmed the formation of crystallinity and development of MFI structure in the mesoporous silicalite-1. The adsorption of MB dye on mesoporous silicalite-1 was conducted by batch adsorption method. The effect of various parameters such as adsorbent dosage, initial dye concentration, contact time and temperature on the dye uptake ability of silicalite-1 was investigated. The operating parameters for the maximum adsorption are silicalite-1 dosage (0.1 wt%), contact time (240 min), initial dye concentration (10 ppm) and temperature (30 ℃). The MB dye removal onto mesoporous silicalite-1 followed pseudo-second-order kinetic and Freundlich isotherm. The silicalite-1 exhibits 86% removal efficiency even after six adsorption–desorption cycle. Therefore, the developed mesoporous silicalite-1 is an effective eco-friendly adsorbent for MB dye removal from aqueous environment.


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