scholarly journals Electrochemical Removal of Chromium (VI) from Wastewater

2019 ◽  
Vol 9 (6) ◽  
pp. 1156 ◽  
Author(s):  
Hao Peng ◽  
Yumeng Leng ◽  
Jing Guo

The removal of hexavalent chromium has attracted much attention as it is a hazardous contaminant. Electrochemical reduction technology was applied to remove chromium (VI) from wastewater. The mechanisms and parameters that affect the reduction process were investigated. The results showed that the reduction efficiency was significantly affected by the concentration of H2SO4, current density, and reaction temperature. The reduction efficiency was up to 86.45% at an H2SO4 concentration of 100 g/L, reaction temperature of 70 °C, current density at 50 A/m2, reaction time at 180 min, and stirring rate of 500 rpm. The reduction process of chromium (VI) followed a pseudo-first-order equation, and the reduction rate constant could be expressed as Kobs = k [H2SO4]1·[j]4·exp−4170/RT.

Author(s):  
Hao Peng ◽  
Yumeng Leng ◽  
Jing Guo

Removal of hexavalent chromium had attracted much more attention as it was a hazardous contaminant. Electrochemical reduction technology was applied to removal chromium (VI) from wastewater. The mechanism and parameters affect the reduction process were investigated. The results showed that the reduction efficiency was significantly affected by the concentration of H2SO4, current density and reaction temperature. And the reduction efficiency was up to 86.45% at concentration of H2SO4 of 100g/L, reaction temperature of 70 ℃, current density at 50 A/m2, reaction time at 180 min and stirring rate of 500 rpm. The reduction process of chromium (VI) was followed pseudo-first-order equation, and the reduction rate could be expressed as Kobs = k [H2SO4]1• [j] 4•exp-4170/RT.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Hao Peng ◽  
Jing Guo

Abstract The direct Cr(VI) reduction process by oxalic acid was conducted. The existence of Cr(VI) in the reaction medium was measured by software Visual MINTEQ and the concentration of Cr(VI) was measured by ICP-OES. The results showed that the Cr(VI) was efficiently reduced by oxalic acid at high reaction temperature and high dosage of oxalic acid. The reduced product, Cr(III), was easily generated stable complex compounds (Cr(HC2O4)3) with oxalate, which displayed a negative effect on the reduction process. The high reaction temperature and high acidic medium could destroy the stable structure of a complex compound to release oxalate, and facilitate the reduction of Cr(VI). Generally, the results showed in this paper provided a versatile strategy for Cr(VI) reduction and exhibited a bright application future for real wastewater treatment.


Author(s):  
Hao Peng ◽  
Jing Guo ◽  
Binfang Yuan ◽  
Liping Lv ◽  
Huisheng Huang ◽  
...  

The direct Cr (VI) reduction process by oxalic acid was conducted and the results showed that the Cr (VI) was efficiently reduced by oxalic acid at high reaction temperature and high dosage of oxalic acid. The reduced product, Cr (III), was easily generated stable complex compounds (Cr(HC2O4)3) with oxalate, which displayed a negative effect on the reduction process. The high reaction temperature and high acidic medium could destroy the stable structure of a complex compound to release oxalate, and facilitate the reduction of Cr (VI). Generally, the present study provided a versatile strategy for Cr (VI) reduction, exhibiting a bright application future for real wastewater treatment.


2010 ◽  
Vol 7 (1) ◽  
pp. 299-307 ◽  
Author(s):  
S. Sophie Beulah ◽  
K. Muthukumaran

High temperature activatedSyzygium Jambolanumnut carbon (HSJC) has been effectively used for the removal of Cr(VI) and Hg(II) from aqueous solution by batch experiments. Effect of pH, carbon dose and equilibration time were determined. Adsorption followed Freundlich and Langmuir isotherms. Kinetic studies indicated that the removal process followed reversible first order equation. Desorption of Cr(VI) was done with 1 M NaOH and 10% H2O2mixture and Hg(II) with 2% Na2S in 1% NaOH. The performance of HSJC was compared with a commercial activated carbon (CAC).


2020 ◽  
Vol 1 (4) ◽  
Author(s):  
Peizeng Yang ◽  
Yaye Wang ◽  
Junhe Lu ◽  
Viktor Tishchenko ◽  
Qingguo Huang ◽  
...  

This study examined the degradation of perfluorooctanesulfonate (PFOS) in electrochemical oxidation (EO) processes in the presence of trichloroethylene (TCE). The EO experiment was performed in a gas-tight reactor using Magnéli phase titanium suboxide (Ti4O7) as the anode. The experimental data demonstrated that 75% of PFOS (2 μM) was degraded at 10 mA/cm2 current density in 30 min without TCE present in the solution, while the presence of 76 μM TCE apparently inhibited the degradation of PFOS, reducing its removal down to 53%. Defluorination ratio suggested that PFOS was significantly mineralized upon EO treatment, and it appeared to be not influenced by the presence of TCE. The respective pseudo-first order rate constants (kobs) of PFOS removal were 0.0471 and 0.0254 min-1 in the absence and presence of TCE. The degradation rates of both PFOS and TCE increased with current density rising from 2.5 to 20 mA/cm2. In the presence of TCE, chloride, chlorate, and perchlorate were formed that accounted for 79.7 %, 5.53%, and 1.51% of the total chlorine at 60 min. This work illustrates the promise of the Magnéli phase Ti4O7 electrode based electrochemical oxidation technology for degrading per- and polyfluoroalkyl substances (PFASs) and co-contaminants in groundwaters.


Author(s):  
Zhiyuan Chen ◽  
Christiaan Zeilstra ◽  
Jan van der Stel ◽  
Jilt Sietsma ◽  
Yongxiang Yang

AbstractIn order to understand the pre-reduction behaviour of fine hematite particles in the HIsarna process, change of morphology, phase and crystallography during the reduction were investigated in the high temperature drop tube furnace. Polycrystalline magnetite shell formed within 200 ms during the reduction. The grain size of the magnetite is in the order of magnitude of 10 µm. Lath magnetite was observed in the partly reduced samples. The grain boundary of magnetite was reduced to molten FeO firstly, and then the particle turned to be a droplet. The Johnson-Mehl-Avrami-Kolmogorov model is proposed to describe the kinetics of the reduction process. Both bulk and surface nucleation occurred during the reduction, which leads to the effect of size on the reduction rate in the nucleation and growth process. As a result, the reduction rate constant of hematite particles increases with the increasing particle size until 85 µm. It then decreases with a reciprocal relationship of the particle size above 85 µm.


2015 ◽  
Vol 713-715 ◽  
pp. 2909-2912
Author(s):  
Bin Zhao ◽  
Li Ke Zou ◽  
Guo Yong Li

Cuprous oxide catalyst was prepared and applied as photocatalist to treat chromium (VI) in wastewater, and the photocatalytic activity of the cuprous oxide was studied. The optimal conditions for the treatment was as follows: the pH of wastewater was 3, the amount of catalysts was 0.3 g/L, the reaction temperature was 60°C. Under the optimal conditions, the removal rate of chromium (IV) in wastewater reached 50% in the presence of cuprous oxide catalyst.


2012 ◽  
Vol 27 (14) ◽  
pp. 1250081 ◽  
Author(s):  
S. I. KRUGLOV

We postulate the second-order derivative equation with four parameters for spin-1/2 fermions possessing two mass states. For some choice of parameters fermions propagate with the superluminal speed. Thus, the novel tachyonic equation is suggested. The relativistic 20-component first-order wave equation is formulated and projection operators extracting states with definite energy and spin projections are obtained. The Lagrangian formulation of the first-order equation is presented and the electric current and energy–momentum tensor are found. The minimal and nonminimal electromagnetic interactions of fermions are considered and Schrödinger's form of the equation and the quantum-mechanical Hamiltonian are obtained. The canonical quantization of the field in the first-order formalism is performed and we find the vacuum expectation of chronological pairing of operators.


2021 ◽  
pp. 2151037
Author(s):  
Yu Meng ◽  
Qing Zhong ◽  
Arzugul Muslim

Because −NH2 and −NH− in poly-[Formula: see text]-phenylenediamine (P[Formula: see text]PD) can interact strongly with the empty orbitals of Cu to show unique electrochemical activity, P[Formula: see text]PD is suitable for the removal of Cu[Formula: see text] by electrochemical oxidation–reduction process. In this study, with P[Formula: see text]PD and its carbon dot composite (CDs/P[Formula: see text]PD) as working electrodes, the electrochemical reduction and removal of Cu[Formula: see text] in the aqueous solution were carried out with the potentiostatic method. According to effects of voltage, pH of the solution, initial concentration of Cu[Formula: see text], and electrochemical reduction time on the Cu[Formula: see text] removal, the Cu[Formula: see text] removal ratios of P[Formula: see text]PD and CDs/P[Formula: see text]PD were up to 64.69% and 73.34%, respectively, at −0.2 V and the optimal pH. Additionally, results showed that these processes were in line with the quasi-first order kinetic model. Both P[Formula: see text]PD and CDs/P[Formula: see text]PD showed good reproducibility in six cycles. After five times of repeated usage, the regeneration efficiencies of P[Formula: see text]PD and CDs/P[Formula: see text]PD dropped to 77.04% and 79.36%, respectively.


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