Experimental and model studies on comparison of As(III and V) removal from synthetic acid mine drainage by bone char

2014 ◽  
Vol 78 (1) ◽  
pp. 73-89 ◽  
Author(s):  
Jing Liu ◽  
Xi Huang ◽  
Juan Liu ◽  
Weiqing Wang ◽  
Wei Zhang ◽  
...  

AbstractAcid mine drainage (AMD) commonly contains elevated concentrations of As(III) and/or As(V) due to oxidation of arsenic-containing sulfides. Bone char has been used as a low-cost filling material for passive treatment. The breakthrough curves of As(III) and As(V) were studied in column experiments conducted at different flow rates, adsorption cycle times, and with different coexisting cations and anions to compare their transport behaviours. The experimental data were fitted by the Convection- Diffusion Equation (CDE) and Thomas model with the aim of obtaining retardation factors of As(III) and As(V) and their maximum adsorption capacities, respectively. The maximum adsorption capacities of As(III) and As(V) are 0.214 and 0.335 mg/g, respectively. Coexisting Mn2+ and Al3+ ions can shorten the equilibrium time of As(V) adsorption from 25 h to 8 h, but they have little effect on As(III). The retardation factors of As(III) and As(V) calculated by the CDE model decrease with adsorption cycles from 37 to 20 and 51 to 32, respectively. The Mn2+ and Al3+ ions could enhance retention ability with adsorption cycle time, especially Mn2+ for As(V). Secondary adsorption phenomena were observed only in breakthrough curves of As(V) in the presence of Mn2+ and Al3+. The competitive influences of coexisting arsenic species is As(V) > As(III). Regeneration experiments using distilled water and NaOH solution were completed to quantify the degree of desorption of both As(III) and As(V). The results show that As(V) adsorbed on bone char has better desorption performance than As(III), and the average degrees of desorption of As(III) and As(V) for three desorption experiments are 75% and 31%, respectively.

2021 ◽  
Vol 11 (2) ◽  
Author(s):  
Tebogo M. Mokgehle ◽  
Nikita T. Tavengwa

AbstractAcid mine drainage is the reaction of surface water with sub-surface water located on sulfur bearing rocks, resulting in sulfuric acid. These highly acidic conditions result in leaching of non-biodegradeable heavy metals from rock which then accumulate in flora, posing a significant environmental hazard. Hence, reliable, cost effective remediation techniques are continuously sought after by researchers. A range of materials were examined as adsorbents in the extraction of heavy metal ions from acid mine drainage (AMD). However, these materials generally have moderate to poor adsorption capacities. To address this problem, researchers have recently turned to nano-sized materials to enhance the surface area of the adsorbent when in contact with the heavy metal solution. Lately, there have been developments in studying the surface chemistry of nano-engineered materials during adsorption, which involved alterations in the physical and chemical make-up of nanomaterials. The resultant surface engineered nanomaterials have been proven to show rapid adsorption rates and remarkable adsorption capacities for removal of a wide range of heavy metal contaminants in AMD compared to the unmodified nanomaterials. A brief overview of zeolites as adsorbents and the developent of nanosorbents to modernly applied magnetic sorbents and ion imprinted polymers will be discussed. This work provides researchers with thorough insight into the adsorption mechanism and performance of nanosorbents, and finds common ground between the past, present and future of these versatile materials.


2012 ◽  
Vol 27 (10) ◽  
pp. 1944-1952 ◽  
Author(s):  
Aguasanta M. Sarmiento ◽  
Manuel A. Caraballo ◽  
Daniel Sanchez-Rodas ◽  
José Miguel Nieto ◽  
Annika Parviainen

2012 ◽  
Vol 161 ◽  
pp. 200-204 ◽  
Author(s):  
Shuai Wang ◽  
Gang Zhao ◽  
Zhong Nan Wang ◽  
Qian Zhang ◽  
Hong Zhong

Acid solution and copper-containing acid mine drainage (AMD) was treated by neutralization-adsorption process. The results showed that pH can be adjusted to 4.0 by adding 10g·L-1calcite in acid solution with pH=1.0. Adsorption and desorption performance of poly(hydroxamic acid) (PHA) resin for Cu2+and Fe3+ions were investigated by column tests. The results showed that adsorption capacities of PHA for Cu2+and Fe3+ions were satisfying, and the metals adsorbed on PHA can be eluted by sulfuric acid solution effectively. AMD of Dexing copper mine of Jiangxi was treated as a sample. The results showed that 1.5g·L-1calcite can remove almost all of the Fe3+ion, and Cu2+ion can be removed by PHA and then be eluted by sulfuric acid solution with adsorption ratio of 98.95% and elution ratio of 98.50%, separately.


Molecules ◽  
2021 ◽  
Vol 26 (21) ◽  
pp. 6615
Author(s):  
Konstantin B. L. Borchert ◽  
Christine Steinbach ◽  
Berthold Reis ◽  
Niklas Gerlach ◽  
Philipp Zimmermann ◽  
...  

Due to the existence-threatening risk to aquatic life and entire ecosystems, the removal of oxyanions such as sulfate and phosphate from anthropogenic wastewaters, such as municipal effluents and acid mine drainage, is inevitable. Furthermore, phosphorus is an indispensable resource for worldwide plant fertilization, which cannot be replaced by any other substance. This raises phosphate to one of the most important mineral resources worldwide. Thus, efficient recovery of phosphate is essential for ecosystems and the economy. To face the harsh acidic conditions, such as for acid mine drainage, an adsorber material with a high chemical resistivity is beneficial. Poly(melamine-co-formaldehyde) (PMF) sustains these conditions whilst its very high amount of nitrogen functionalities (up to 53.7 wt.%) act as efficient adsorption sides. To increase adsorption capacities, PMF was synthesized in the form of mesoporous particles using a hard-templating approach yielding specific surface areas up to 409 m2/g. Different amounts of silica nanospheres were utilized as template and evaluated for the adsorption of sulfate and phosphate ions. The adsorption isotherms were validated by the Langmuir model. Due to their properties, the PMF particles possessed outperforming maximum adsorption capacities of 341 and 251 mg/g for phosphate and sulfate, respectively. Furthermore, selective adsorption of sulfate from mixed solutions of phosphate and sulfate was found for silica/PMF hybrid particles.


2020 ◽  
Vol Special Issue (1) ◽  

Acid Mine Drainage (AMD) exists as a phenomenon that involves the release of acidic water and metal conjugates, in and around mines, degrading the surrounding water environment. A real-time mining effluent is treated using low-cost adsorption technology using Combined Vegetable Waste Carbon (CVWC) as sorbent. Batch sorption was reviewed to know the effect of process factors on the removal of Cadmium (Cd), Zinc (Zn), and Iron (Fe). A two-level CCD (Central Composite Design) with three factors was adopted in the optimization of process factors. Also, the same factors were considered to review the ANNs (Artificial Neural Networks), model. A comparative statistical analysis was performed for the experimental data based on RMSE and R2 values in both RSM (Response Surface Methodology) and ANNs models. This study revealed that the ANNs model was well fit compared to RSM and this would probably reduce the experimental trials thereby reducing cumbersome calculations.


2014 ◽  
Vol 11 (5) ◽  
pp. 514 ◽  
Author(s):  
Marina Héry ◽  
Corinne Casiot ◽  
Eléonore Resongles ◽  
Zoe Gallice ◽  
Odile Bruneel ◽  
...  

Environmental context Arsenic-rich waters generated from the oxidation of mining wastes are responsible for the severe contamination of river waters and sediments located downstream from mining sites. Under certain environmental conditions, the affected riverbed sediments may represent a reservoir for arsenic from which this toxic element may be released into water, mainly as a consequence of microbial activity. Abstract The (bio-)geochemical processes driving As mobilisation from streambed sediments affected by acid mine drainage (AMD) were investigated, and the structure of the bacterial community associated with the sediments was characterised. Microcosm experiments were set up to determine the effect of oxygen, temperature (4 and 20°C) and microbial activity on As mobilisation from contrasting sediments collected during high- (November 2011) and low- (March 2012) flow conditions in the Amous River, that received AMD. Distinct bacterial communities thrived in the two sediments, dominated by Rhodobacter spp., Polaromonas spp. and Sphingomonads. These communities included only few bacteria known for their capacity to interact directly with As, whereas biogeochemical processes appeared to control As cycling. Major As mobilisation occurred in the AsIII form at 20°C in anoxic conditions, from both November and March sediments, as the result of successive biotic reductive dissolution of Mn- and Fe-oxyhydroxides. The later process may be driven by Mn- and Fe-reducing bacteria such as Geobacter spp. and possibly occurred in combination with microbially mediated AsV reduction. The involvement of other bacteria in these redox processes is not excluded. Biomethylation occurred only with the sediments collected at low-flow during oxic and anoxic conditions, although no bacteria characterised so far for its ability to methylate As was identified. Finally, sorption equilibrium of AsV onto the sediment appeared to be the main process controlling AsV concentration in oxic conditions. Comparison with field data shows that the later process, besides biomethylation, may be of relevance to the As fate in AMD-affected streams.


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