Parametric study of the removal efficiency of divalent copper ions onto drilling cutting ashes

2020 ◽  
Vol 20 (2020) ◽  
pp. 150-151
Author(s):  
Kilton Renan Alves Pereira ◽  
Fabio Pereira Fagundes ◽  
Danielly da Silva Costa ◽  
Francisco Adeilson Rocha ◽  
Sabrina da Silva De Souza ◽  
...  
2021 ◽  
Vol 13 (8) ◽  
pp. 4184
Author(s):  
Zhiying Xu ◽  
Caterina Valeo ◽  
Angus Chu ◽  
Yao Zhao

This research investigates the use of a common food waste product for removing four different types of metals typically found in stormwater. Whole, unprocessed oyster shells are explored for use in stormwater management infrastructure that addresses water quality concerns. The role of the shells’ surface area, exposure time, and the solution’s initial concentration on the removal efficiency were examined. Beaker scale experimental results demonstrated very good efficiency by the oyster shells for removing copper ions (80–95%), cadmium ions (50–90%), and zinc ions (30–80%) but the shells were not as effective in removing hexavalent chromium (20–60%). There was a positive relationship between initial concentration and removal efficiency for copper and zinc ions, a negative relationship for hexavalent chromium, and no relationship was found for cadmium ions. There was also a positive relationship between surface area and removal efficiency, and exposure time and removal efficiency. However, after a certain exposure time, the increase in removal efficiency was negligible and desorption was occasionally observed. A mid-scale experiment to mimic real-world conditions was conducted in which continuous inflow based on a 6-h design storm was applied to 2.7 kg of whole, unprocessed oyster shells. The shells provided an 86% and an 84% removal efficiency of cadmium and copper ions, respectively, in one day of hydraulic retention time. No removal was observed for hexavalent chromium, and zinc ion removal was only observed after initial leaching. This work has significant implications for sustainable stormwater infrastructure design using a material commonly found in municipal food waste.


Author(s):  
D. V. Tolkachev ◽  
A. A. Khodak ◽  
S. P. Solodovnikov ◽  
N. N. Bubnov ◽  
M. I. Kabachnik

2021 ◽  
Author(s):  
Magal Saphier ◽  
Lea Moshkovich ◽  
Stanislav Popov ◽  
Yoram Shotland ◽  
Eldad Silberstein ◽  
...  

Abstract The effect of monovalent copper ions on enzymatic systems has hardly been studied to date; this is due to the low stability of monovalent copper ions in aqueous solutions, which led to the assumption that their concentration is negligible in biological systems. However, in an anaerobic atmosphere, and in the presence of a ligand that stabilizes the monovalent copper ions over the divalent copper ions, high and stable concentrations of monovalent copper ions can be reached. Moreover, the cell cytoplasm has a substantial concentration of potential stabilizers that can explain significant concentrations of monovalent copper ions in the cytoplasm. This study demonstrates the effect of monovalent and divalent copper ions on DNA polymerase, ligaseT4 DNA, the restriction enzymes EcoP15I and EcoR I, acid phosphatase, and α and βamylase enzymes. These systems were chosen because they can be monitored under conditions necessary for maintaining a stable concentration of monovalent copper ions, and since they exhibit a wide range of dependency on ATP. Previous studies indicated that ATP interacts with monovalent and divalent copper ions and stabilizing monovalent copper ions over divalent copper ions. The results showed that monovalent copper ions dramatically inhibit DNA polymerase and acid phosphatase, inhibit ligaseT4 DNA and the restriction enzyme EcoP15I, moderately inhibit α and β amylase, and have no effect on the restriction enzyme EcoR I. From the results presented in this work, it can be concluded that the mechanism is not one of oxidative stress, even though monovalent copper ions generate reactive oxygen species (ROS). Molecular oxygen in the medium, which is supposed to increase the oxidative stress, impairs the inhibitory effect of monovalent and divalent copper ions, and the kinetics of the inhibition is not suitable for the ROS mechanism.ATP forms a complex with copper ions (di and monovalent ions, where the latter is more stable) in which the metal ion is bound both to the nitrogen base and to the oxygen charged on the phosphate groups, forming an unusually distorted complex. The results of this study indicate that these complexes have the ability to inhibit enzymatic systems that are dependent on ATP.This finding can provide an explanation for the strong antimicrobial activity of monovalent copper ions, suggesting that rapid and lethal metabolic damage is the main mechanism of monovalent copper ions’ antimicrobial effect.


1984 ◽  
Vol 25 (3-4) ◽  
pp. 237-241 ◽  
Author(s):  
G. P. Potapov ◽  
E. I. Kazakova ◽  
V. A. Poluboyarov ◽  
V. F. Anufrienko

2015 ◽  
Vol 3 (3) ◽  
pp. 1265-1271 ◽  
Author(s):  
Xun Qiu ◽  
Najun Li ◽  
Shun Yang ◽  
Dongyun Chen ◽  
Qingfeng Xu ◽  
...  

A new core–shell structured magnetic nanocomposite (SDMA) was successfully prepared for simultaneous detection and removal of trace Cu2+. In this facile strategy, the new nanocomposites could detect and adsorb trace Cu2+from water with high capacity and good removal efficiency.


2015 ◽  
Vol 21 (4) ◽  
pp. 465-476
Author(s):  
Jun Tan ◽  
Xiaoyan Wei ◽  
Yuxia Ouyang ◽  
Rui Liu ◽  
Ping Sun ◽  
...  

The effectiveness of insoluble xanthate (ISX) and crosslinked starch-graft-polyacrylamide-co-sodium xanthate (CSAX) for Cu(II) removal from wastewater was evaluated. The two types of xanthates were characterized by SEM, XRD, FTIR, and elemental analysis. Also, the factors influencing adsorption behaviors of copper ions from aqueous solutions were investigated. The results indicated CSAX had higher absorption capacity for Cu(II) than ISX because it contained more N and S. While as far as the removal efficiency was concerned, ISX was better than CSAX for its strong ligand-CSS- groups. The removal efficiency of Cu(II) onto CSAX and ISX increased with the increase in pH. The mechanism for Cu(II) adsorption was ionic exchange for ISX whereas both ion exchange and physical adsorption contributed to adsorption by CSAX. The adsorption kinetics of ISX and CSAX for Cu(II) were favorably described by the pseudo-second-order kinetic model, and the adsorption isotherms were described well with the Freundlich isotherm model. The study with synthetic wastewater showed CSAX was a worthwhile alternative to the traditional ISX only when the wastewater contained both Cu(II) and turbidity.


2018 ◽  
Vol 32 (14) ◽  
pp. 1850172 ◽  
Author(s):  
B. B. V. S. Vara Prasad ◽  
K. V. Ramesh ◽  
Adiraj Srinivas

Nanocrystalline Co[Formula: see text]Zn[Formula: see text]Cu[Formula: see text]Fe2O4 spinel ferrites were prepared by autocombustion method with citric acid as fuel. Paramagnetic divalent copper ions substituted in place of ferromagnetic cobalt ions resulted in the modifications of structural and magnetic properties of the system. All samples were characterized with X-ray diffraction technique for structure determination. Crystallite sizes were calculated using Williamson–Hall plot and size–strain plots. Cation distribution and all other structural parameters were presented. Transmission electron microscopy measurements were done for x = 0 and x = 0.15 and they showed well-developed spherical particles with average sizes of 35 nm and 48 nm. Morphological studies were performed and grain growth was observed to be increased with copper concentration. EDAX measurements revealed the stoichiometric proportions of the samples as per the chemical composition. Mid-IR spectroscopy was used to characterize the spinel phase and displayed two characteristic absorption bands in all samples with a slight shift. M–H loops were recorded using vibrating sample magnetometer at room-temperature and highest saturation magnetization was observed to be 50.2 emu/g for the base (x = 0) sample. Magnetocrystalline anisotropy was discussed with the help of magnetocrystalline anisotropy constant K1.


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