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"Arsenic removal"
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Biochar Adsorbents for Arsenic Removal from Water Environment: A Review
Arsenic intake can cause human health disorders to the lungs, urinary tract, kidney, liver, hyper-pigmentation, muscles, neurological and even cancer. Biochar is potent, economical and ecologically sound adsorbents for water purification. After surface modifications, adsorption capacity of biochar significantly increased due to high porosity and reactivity. Adsorption capacities of the biochar derived from the municipal solid waste and KOH mixed municipal solid waste were increased from 24.49 and 30.98 mg/g for arsenic adsorption. Complex formation, electrostatic behavior and ion exchange are important mechanisms for arsenic adsorption. Organic arsenic removal using biochar is a major challenge. Hence, more innovative research should be conducted to achieve one of the 17 sustainable development goals of the United Nations i.e. “providing safe drinking water for all”. This review is focused on the arsenic removal from water using pristine and modified biochar adsorbents. Recent advances in production methods of biochar adsorbents and mechanisms of arsenic removal from water are also illustrated.
Journal Article
Arsenic removal methods for drinking water in the developing countries: technological developments and research needs
Arsenic pollution of drinking water is a concern, particularly in the developing countries. Removal of arsenic from drinking water is strongly recommended. Despite the availability of efficient technologies for arsenic removal, the small and rural communities in the developing countries are not capable of employing most of these technologies due to their high cost and technical complexity. There is a need for the “low-cost” and “easy to use” technologies to protect the humans in the arsenic affected developing countries. In this study, arsenic removal technologies were summarized and the low-cost technologies were reviewed. The advantages and disadvantages of these technologies were identified and their scopes of applications and improvements were investigated. The costs were compared in context to the capacity of the low-income populations in the developing countries. Finally, future research directions were proposed to protect the low-income populations in the developing countries.
Journal Article
Enhancement of 15% calcium oxide doped nano zero-valent iron on arsenic removal from high-arsenic acid wastewater
Nano zero-valent iron (nZVI) has a great potential for arsenic removal, but it would form aggregates easily and consume largely by H
+
in the strongly acidic solution. In this work, 15%CaO doped with nZVI (15%CaO-nZVI) was successfully synthesized from a simplified ball milling mixture combined with a hydrogen reduction method, which had a high adsorption capacity for As(V) removal from high-arsenic acid wastewater. More than 97% As(V) was removed by 15%CaO-nZVI under the optimum reaction conditions of pH 1.34, initial As(V) concentration 16.21 g/L, and molar ratio of Fe/As (
n
Fe
/
n
As
) 2.5:1. The effluent pH solution was weakly acidic 6.72, and the secondary arsenic removal treatment reduced the solid waste and improved arsenic grade in slag from the mass fraction of 20.02% to 29.07%. Multiple mechanisms including Ca
2+
enhanced effect, adsorption, reduction, and co-precipitation coexisted for As(V) removal from high-arsenic acid wastewater. Doping of CaO might lead to improving cracking channels which was benefit for electronic transmission and the confusion of atomic distribution. The in situ weak alkaline environment generated on the surface of 15%CaO-nZVI would increase the content of γ-Fe
2
O
3
/Fe
3
O
4
, which was in favor for As(V) adsorption. In addition, H
+
in the strongly acidic solution could accelerate corrosion of 15%CaO-nZVI and abundant fresh and reactive iron oxides continuously generated, which would provide plenty specific reactive site and fast charge transfer and ionic mobility for arsenic removal.
Journal Article
Statistical-based optimization and mechanism assessments of Arsenic (III) adsorption by ZnO-Halloysite nanocomposite
Arsenic contamination in aqueous media is a serious environmental problem, especially in developing countries. In this research, the Box-Behnken response surface methodology was used to optimize the most relevant variables affecting arsenic adsorption on the ZnO-halloysite surface, including temperature, adsorbent dosage, pH, contact time, and As (III) initial concentration. The regression analysis indicated that the experimental data were appropriately fitted to a quadratic model with the adjusted R-squared value (R
2
) of 0.982 for As(III) adsorption capacity and a linear model with R
2
of 0.931 for As(III) removal. The p-values for both adsorption capacity and removal efficiency were below 0.05, with F-values of 116.91 and 115.58, respectively, supporting the model’s validity. The optimum conditions for maximum removal of As(III) were determined through numerical and graphical optimization using the desirability function. It was found that the optimum conditions for adsorption were pH = 7.99, contact time of 3.99 h, As(III) initial concentration of 49.96 mg/L, and adsorbent dosage of 0.135 g/40 ml. The accuracy of the optimization procedure was confirmed by a confirmatory experiment, which showed a maximum arsenic removal of 91.31% and an adsorption capacity of 12.63 mg/g under optimized conditions. Moreover, XPS analysis was performed at different pH levels to investigate the As (III) adsorption mechanism. The results demonstrated that As(III) adsorption occurs at acidic and neutral pH levels. On the other hand, when pH is increased to 8, As (III) oxidizes to As (V), and then adsorption occurs.
Journal Article
Arsenic Contamination of Groundwater Is Determined by Complex Interactions between Various Chemical and Biological Processes
At a great many locations worldwide, the safety of drinking water is not assured due to pollution with arsenic. Arsenic toxicity is a matter of both systems chemistry and systems biology: it is determined by complex and intertwined networks of chemical reactions in the inanimate environment, in microbes in that environment, and in the human body. We here review what is known about these networks and their interconnections. We then discuss how consideration of the systems aspects of arsenic levels in groundwater may open up new avenues towards the realization of safer drinking water. Along such avenues, both geochemical and microbiological conditions can optimize groundwater microbial ecology vis-à-vis reduced arsenic toxicity.
Journal Article
Study on the Effect of Calcium Alloy on Arsenic Removal from Scrap-Based Steel Production
Scrap steel is a kind of resource that can be recycled indefinitely. However, the enrichment of arsenic in the recycling process will seriously affect the performance of the product, making the recycling process unsustainable. In this study, the removal of arsenic from molten steel using calcium alloys was investigated experimentally, and the underlying mechanism was explored based on thermodynamic principles. The results show that the addition of calcium alloy is an effective means of reducing the arsenic content in molten steel, with the highest removal percentage of 56.36% observed with calcium aluminum alloy. A thermodynamic analysis revealed that the critical calcium content required for arsenic removal reaction is 0.0037%. Moreover, ultra-low levels of oxygen and sulfur were found to be crucial in achieving a good arsenic removal effect. When the arsenic removal reaction occurs in molten steel, the oxygen and sulfur concentrations in equilibrium with calcium were wO=0.0012% and wS=0.00548%, respectively. After successful arsenic removal, the arsenic removal product of the calcium alloy is Ca3As2, which usually does not appear alone. Instead, it is prone to combining with alumina, calcium oxide, and other inclusions to form composite inclusions, which is beneficial for the floating removal of inclusions and the purification of scrap steel in molten steel.
Journal Article
Field Testing of an Affordable Zero-Liquid-Discharge Arsenic-Removal Technology for a Small-Community Drinking Water System in Rural California
Arsenic contamination in groundwater threatens public health, particularly in small, low-income communities lacking affordable treatment solutions. This study investigated the field implementation of novel air cathode assisted iron electrocoagulation (ACAIE) technology for arsenic removal in Allensworth, California, where groundwater arsenic concentrations exceeded 250 µg/L. Over four months, a pilot-scale ACAIE system, operating at 600 L/h, consistently reduced arsenic levels to below the EPA’s maximum contaminant level of 10 µg/L. Laboratory experiments informed the optimization of charge dosage and flow rates, which were validated during field testing of the ACAIE 600 L/h system. The in-situ generation of hydrogen peroxide at the cathode speeded up the reaction kinetics, ensuring high arsenic removal efficiency while allowing high throughput, even with a compact reactor size. An economic analysis demonstrated a treatment cost of USD 0.02/L excluding labor, highlighting the system’s affordability compared to conventional methods. Adding labor costs increased the treatment cost to USD 0.09/L. The regeneration of air cathodes extended their operational life, addressing a key maintenance challenge, thus reducing the costs slightly. Intermittent challenges were encountered with filtration and secondary contaminant removal; these issues highlight opportunities for further operational improvements. Despite these challenges, ACAIE’s low operational complexity, scalability, and cost-effectiveness make it a promising solution for underserved small communities. These findings provide critical insights into deploying sustainable arsenic remediation technologies that are tailored to the needs of rural, low-resource communities.
Journal Article
A two-step approach for arsenic removal by exploiting an autochthonous Delftia sp. BAs29 and neutralized red mud
Groundwater arsenic contamination represents a global threat to human health. Among the proposed bioremediation applications, microbial transformation of arsenite (As (III)) seems to be the most favorable approach as it can be easily coupled with several adsorption techniques, without producing lethal by-products or demanding chemical addition. This study highlights the potential contribution of a highly efficient As (III) transforming bacteria
Delftia
sp. BAs29 followed by the adsorption of transformed arsenate (As (V)) using neutralized red mud under suitable treatment conditions. Diverse experimental conditions elucidated (inflow As (III) concentrations, flow rate) the rate and oxidation efficiency to mediate the process. Red mud is a waste by-product from the Bayer’s process of the alumina industry, which when neutralized aids the removal of As (V). The neutralized red mud was characterized using X-ray diffraction (XRD) microanalysis, Scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM-EDX) and Fourier-transform infrared spectroscopy (FTIR). Arsenate adsorption using neutralized red mud was also studied as a function of pH and time, adsorbent dosage, and initial As (V) concentration. The adsorption process was significantly affected by the solution pH, which on decreasing gradually increased the adsorption efficiency. The maximum monolayer capacity for adsorption of 274.1 mg/g As (V) was found at optimum conditions of pH 4.0 and a contact time of 30 min at a temperature of 30 °C, respectively. Furthermore, this process significantly contributed in fabricating a two-step bio-filter column for the removal of total arsenic from groundwater.
Graphical abstract
Journal Article
Evaluating of arsenic(V) removal from water by weak-base anion exchange adsorbents
Arsenic contamination of groundwater has been called the largest mass poisoning calamity in human history and creates severe health problems. The effective adsorbents are imperative in response to the widespread removal of toxic arsenic exposure through drinking water. Evaluation of arsenic(V) removal from water by weak-base anion exchange adsorbents was studied in this paper, aiming at the determination of the effects of pH, competing anions, and feed flow rates to improvement on remediation. Two types of weak-base adsorbents were used to evaluate arsenic(V) removal efficiency both in batch and column approaches. Anion selectivity was determined by both adsorbents in batch method as equilibrium As(V) adsorption capacities. Column studies were performed in fixed-bed experiments using both adsorbent packed columns, and kinetic performance was dependent on the feed flow rate and competing anions. The weak-base adsorbents clarified that these are selective to arsenic(V) over competition of chloride, nitrate, and sulfate anions. The solution pH played an important role in arsenic(V) removal, and a higher pH can cause lower adsorption capacities. A low concentration level of arsenic(V) was also removed by these adsorbents even at a high flow rate of 250–350 h
−1
. Adsorbed arsenic(V) was quantitatively eluted with 1 M HCl acid and regenerated into hydrochloride form simultaneously for the next adsorption operation after rinsing with water. The weak-base anion exchange adsorbents are to be an effective means to remove arsenic(V) from drinking water. The fast adsorption rate and the excellent adsorption capacity in the neutral pH range will render this removal technique attractive in practical use in chemical industry.
Journal Article