Open access peer-reviewed chapter

Removal of Arsenic - “A Silent Killer” in the Environment by Adsorption Methods

Written By

Ashok Kumar, Kaman Singh, Utkarsh Dixit, Rayees Ahmad Bhat and Satya Prakash Gupta

Submitted: June 11th, 2021Reviewed: June 19th, 2021Published: September 8th, 2021

DOI: 10.5772/intechopen.98985

Chapter metrics overview

102 Chapter Downloads

View Full Metrics


Water is one of the most essential requirements for living being to survive because 70–80% of the mass of most living bodies consists of water and various mineral and organic salts. Water is also most important component of our environment. Large amount of water is used in various industries or commercial level or domestic level and finally effluent water is loaded with large amount of pollutants such as organic chemicals (surfactants, dyes, phenols etc.), inorganic hazardous heavy metals (As in present case) microbes (bacteria, fungi etc.) pollutants particulate etc. Arsenic is a natural metalloid chemical that may be present in groundwater and surface water gets polluted, hence, aquatic life of plants and animals is disturbed and cause abnormal growth and various diseases, hence, short term or long term changes occurs in ecosystem. Hence, treatment of wastewater is essentially required before discharge effluent wastewater into ponds or lagoons, drains and rivers. Arsenic is one such element that contaminates the environment as reported in several countries. The largest population at risk is in Bangladesh followed by India (West Bengal). Arsenic is familiar as silent killer because dissolved in water, it is colorless, odorless, and tasteless, yet consumption of relatively small doses of this element in its most toxic forms can cause rapid and violent death. It is a human carcinogen in water over a wide range of pH values, having harmful effects on both human health and environment, even at low concentration. Because of this effect, the World Health Organization (WHO) and the US Environmental Protection Agency (USEPA) set the arsenic standard for drinking water at .010 ppm to protect consumers served by public water systems. Ingestion only poses health problems if a dangerous amount of arsenic enters the body. Then, it can lead to cancer, liver disease, coma, and death. There is no effective treatment for arsenic toxicity. Only the removal of arsenic from aqueous system can prevent the toxicity. A great deal of research over recent decades has been done to lower the concentration of arsenic in drinking water and still there is a need to develop ecofriendly techniques. Existing major arsenic removal technologies include oxidation, adsorption, precipitation, coagulation and membrane separation. This book chapter presents a systematic description of current status of research in the area of arsenic removal from contaminated water and comparison of all technologies available with more emphasis on adsorption.


  • Arsenic
  • Adsorption
  • Environmental and Health Aspects

1. Introduction

Water is one of the most essential requirements for living being to survive because all physiochemical processes of body require aqueous medium this is due to Moreover, 70–80% of the mass of most living bodies consists of water and various mineral and organic salts [1]. Large amount of water is used in various industries or commercial level or domestic level and finally effluent water is loaded with large amount of pollutants such as organic chemicals (surfactants, dyes, phenols, etc.), inorganic hazardous heavy metals (As, Hg, Cd, Pb, etc.) microbes (bacteria, fungi, etc.) pollutants particulate etc. Arsenic is a natural metalloid chemical that may be present in groundwater and surface water gets polluted, hence, aquatic life of plants and animals is disturbed and cause abnormal growth and various diseases, hence, short term or long term changes occurs in ecosystem [2, 3, 4]. Very low concentration (1.50 mg/L) of surfactant is lethal for microorganism, even about 0.50 mg/L is harmful for aquatic life. For human life limit of anionic surfactant concentration should up to 1.0 mg/L. High concentration of surfactant in drinking water causes cancer, irritation, dermatitis, eyes disorder. Water has a broad impact on all aspects of human life including but not limited to health, food, energy, and economy. In addition to the environmental, economic, and social impacts of poor water supply and sanitation, the supply of fresh water is essential for the safety of children and the poor. It is estimated that 10.0–20.0 million people die every year due to waterborne and nonfatal infection causes death of more than 200.0 million people every year. Every day, about 5,000.0–6,000.0 children die due to the water-related problem of diarrhea. There are currently more than 0.78 billion people around the world who do not have access to safe water resources resulting in major health problems [5]. Hence, it increases the permeability of cell membrane, and hence, removal of these pollutants are necessary from industrial and household water [6].

Release of hazardous pollutants and their dispersal in the environment can cause adverse impacts on the environment and to public health [7]. These pollutants are more easily controlled when they are generated than after they are dispersed. It is therefore of prime necessity to design treatment processes that isolate and remove the contaminants at their source [8]. Various methods have been developed in the past decades for treatment of waste water for arsenic as biological, physical and chemical methods. In these methods includes chemical precipitation, flocculation-coagulation [9], electro-flotation, electrochemical destruction, electrochemical coagulation [10], biological degradation [11], ozonation, hydrogen peroxide [12], reverse osmosis [13] etc. All these methods are good but have limited applications and all are very expensive, hence, could not use by small industry for wastewater treatments. For that reason there is need for some conventional method which are economically and ecofriendly for wastewater treatments (As in present case). Adsorption is one of the most extensively applied techniques for the removal of pollutants from the industrial effluents. The prominent and emerging trend of subjecting biosorbents in the adsorption technology is mainly because of their natural existence, abundance, renewable, biodegradable and economic features. The adsorption isotherm equations used to describe the experimental data and the thermodynamic assumptions of the various models [14, 15, 16, 17].


2. Distribution of arsenic in various parts of world water bodies

In the nature arsenic element is found in soil, water and sediments as arsenic oxides. The common chemical oxidation of arsenic in the nature are −3, +3, 0 and + 5.¨, etc. According to the national agency for the research of cancer arsenic compounds are put in group 1 carcinogens [18]. According to World Health Organization the maximum contaminant level of arsenic in the drinking water should not be greater than 10 μg/liter. By the dissolution of minerals, microbial activity arsenic can release into the aquatic environment. Living organism can be affected by arsenic through drinking water. Arsenic polluted water causes damage to central nervous system, kidney, liver, lungs and skin in humans. Further chronic arsenic can cause cardio diseases, hypertension and affects vascular system. Long use of arsenic contaminated water can also cause pigmentation of skin, development of hard paths on the palm of humans. Therefore removal of arsenic from waste water has been remained a subject of concern (Table 1) [17, 18].

Water typeAs contamination (μg/Liter)Ref.
Ground water in various part of world1 -73.6[19]
US Rivers0.1-2[20]
Gomti River, India1.29-9.62[21]
Manchar Lake, Pakistan60.45[22]
Alpine River, France0.1-263[23]
Zenne River, Belgium0.1-263[24]

Table 1.

The distribution of arsenic in natural water can be given as below.


3. Arsenic removal by adsorption

Many methods have been given for Arsenic removal which include chemical precipitation [25], adsorption [26], ion exchange [27], reverse osmosis [28], and electro-dialysis [29]. Out of all these methods adsorption method found to be cheap and best for the removal of arsenic. There are many kinds of adsorbents available for arsenic removal, for their convenient study we can divide them in two categories. The first category is metal and its alloys such as manganese oxide, activated alumina and iron compounds; the second category is activated carbon obtained from red mud, coconut shell and other carbon-like materials. Larger is the surface area of the adsorbent, stronger is its adsorption effect. It is found that that adsorption of As(V) is better than As(III) (Figure 1).

Figure 1.

Different adsorption isotherm models used to describe the experimental data and the thermodynamic assumptions of adsorption method.

3.1 Adsorption isotherm models

3.2 The selection of isotherm models

The Akaike information criterion is used for the selection of appropriate model under the situation of when data fitted by more than one model. The Akaike information criterion is represented as below [30].


Where k is the number of parameters in the model and L is the maximum value of the likelihood function for the model.

3.3 Arsenic removal by iron based adsorbents

Iron based adsorbents are extensively developed and used for the removal of arsenic from water [31] (Table 2). Some adsorbents such as granular ferric hydroxide (GFH) and zero-valent iron have been produced on an industrial scale as commercial adsorbents [39]. Iron oxy-hydroxides are mostly used as the adsorbent because of their easy accessibility. The commonly used iron oxy-hydroxides such as, akaganeite (β-FeOOH), goethite (α-FeOOH), lepidocrocite (γ-FeOOH), ferrihydrites (Fe10O14(OH)2), green rusts can be chemically synthesized by the precipitation of Fe(III) or Fe(+2) salts through the hydrolysis and oxidation processes [40].

AdsorbentsSurface area (m2 g−1)Initial concentration (mg L−1)pHAdsorption capacity (mg g−1) As(III)Adsorption capacity (mg g−1) As (V)Ref.
Granular ferric hydroxide (GFH)240–300As(V):0.16.5-7.51.1[32]
α-FeOOH nanoparticles167.8As(V):1003.076[33]
Ultrafine Fe2O3 nanoparticles1624.04795[34]
Ultrafine FeOOH135As(V): 207.037.3[35]
β -FeOOH nanoparticles330As(V): 207.5120[36]
Magnetite–magnetite nanoparticles49As(III): 1.5
As(V): 1.5
γ -Fe2O3 nanoparticles41-49As(V): 17.02.9[38]

Table 2.

Different iron compounds used as adsorbent for As(III) and As(V) adsorption from aqueous system.

3.4 Adsorption of arsenic using activated carbon (AC)

Activated carbon is the most effective and efficient and most widely used because of its versatile nature and convenient for removal of As(III) and As(V). The activated carbon is micro-porous form of the carbon having large surface area and greater number of pores [41]. Arsenic metal cannot be removed completely by simple chemical or physical treatments. So, in this case, AC is used to remove the toxic metals completely from aqueous solution because there is formation of surface complexes between acidic surface functional groups of AC and the metal ions [42]. The removal efficiency is dependent on various factors, like solution concentration initial pH, ionic strength, adsorbent modification methods, nature of adsorbate, chemical nature of AC, and physical properties (surface area, porosity) [43, 44, 45]. Adsorption of both arsenic is largely affected by environmental factors such as pH solution, ionic strength, and coexisting substances such as anions, cations, and organic matter. The adsorption capacity of the adsorbents depends not only on the surface area, pore volume, and particles size but also on a combination of all factors, surface chemistry, and pore structure. Specific area of the adsorbents does not contribute to the adsorption capacity on the removal of arsenic from water. Therefore selection of the adsorbents for removal of arsenic should be based on a combination of all factors for the adsorbents and adsorbate.

3.4.1 Preparation of adsorbents

There are two different methods for preparation of activated carbon one is physical and other one chemical. Chemical activation is better than physical because it requires lower temperature and global yield is more since burn-off does not require (Figure 2) [45].

Figure 2.

General flow diagram for the preparation of adsorbents.


4. Adsorbents comparison

The adsorption capacity of various adsorbents for the effective removal arsenic employing various adsorption isotherm models have been summarized in Table 3.

AdsorbentsSurface area (m2 g−1)Initial concentration (mg/L)pHCapacity As (III) mg/gmCapacity As (V) mg/gmIsotherm model fittedRef.
Coconut husk20650-6012146.30[46]
Coconut shell with 3% ash1150-12500-20062.4Langmuir[47]
Ce-Ti oxide adsorbent137.4506.57.5Langmuir[48]
Fe3O4 loaded activated carbon3492008204.2Freundlich[49]
Char Carbon36.48157-9922-38934.46[50]
Red mud1307.5-2204.50.5417.642[51]
Pine Leaves1043.27Both Langmuir and Flory-Huggins[52]
Oat Hulls52025-20053.09Langmuir[53]
Iron Impregnated GAC6500-571.95Langmuir[54]
AC (apricot stone)15474.50.034Both Freundlich and Dubinin–Radushkevich[55]
Fe (II) loaded12314.532.023Redlich–Peterson[56]
Fe (III) loaded9874.533.009Redlich–Peterson[57]
Sugar beet pulp8210-59.1-9.40.691Langmuir[58]
Sugar beet pulp-Fe7620-3.58.5-9.12.9Langmuir[59]
Empty fruit bunch biochar18903-3009.418.95.5Langmuir[60]
Rice husk biochar25.163-3008.519.37.1Langmuir[61]
Fe coated empty fruit bunch biochar3-3009.431.415.2Both Langmuir and Freundlich[62]
Fe coated rice husk biochar3-3008.530.716Langmuir[63]
Leonardite char65.681-8074.468.40Langmuir[64]
Tea Waste1-1007189154Langmuir[65]
Concrete Sludge2310-7007175Langmuir[66]
Iron- Chitosan flakes1.441-10716.222.5Langmuir[68]
Iron- Chitosan granules96.81-1072.322.24Langmuir[69]

Table 3.

Different adsorbents and their adsorption capacity for the effective removal As(III) and As(V) employing various adsorption isotherm models.


5. Characteristics of various methods for the removal of arsenic from aqueous system

In order to improve the current analytical methods by removing or treating arsenic from aqueous system, a number of methods have been developed and reviewed in this chapter, which included several method with their characteristics properties (Table 4).

MethodMethod in detailCharacteristicsRef.
PhysicalMixing both contaminated and uncontaminated soilsHigh cost/usage to smaller-scale operations[70, 71, 72]
Washed with sulfuric acid, nitric acid, phosphoric acid, and hydrogen bromideChemicals usage/high cost/usage to smaller-scale operations
Immobilize soluble arsenates using cementSuccessfully used to stabilize As-rich
Emphasis on stabilization/solidification (S/S)Treating As containing wastes in water
Soil flushing using aqueous solutions using surfactants and solvents Adsorption by using specific media,Applied in the field, efficiency can vary from 0% to almost 100%
Chemicalimmobilization, modified coagulation along with filtration, precipitations, immobilizations, and complexation reactionsEconomic but often displayed lower Efficiencies (<90%)[70, 73, 74, 75, 76]
Formation of stable phases, for example, insoluble FeAsO4 (and hydrous species of this compound such as scorodite, FeAsO4.2H2O)Use of selective stabilizing amendments is a challenging task
Stabilization method using nanosized oxides and Fe(0) (particle size of 1 to 100 nm)Gained popularity/high success rate, but it could be expensive when remediating a large area
Intrinsic bioremediationDegradation of arsenic by naturally occurring microorganismMore suitable for remediation of soil with a low level of contaminants[77]
Engineered bioremediationOptimizing the environment condition to promote the proliferation and activity of microorganismsFavorable method used in high contaminated area[78]
Microbial oxidationImmobilization of As in the solid phaseRequired biological activity, and microbiological molecular analysis/involved adsorption or co-precipitation with Fe-ox hydroxides[79]
PhysiochemicalFiltration or coagulation sedimentation, osmosis or electro dialysis, adsorptions, and chemical precipitationsWidely accepted in some places[70, 73, 74, 75, 76]
BiologicalSuch as phytoremediation by using aquatic plants or microbial detoxification of arsenicWidely accepted in some places[70, 73, 74, 75, 76]
PhytoremediationUsing “free-floating plants such as water hyacinth” Using aquatic rooted plants such as Agrostis sp., Pteris vittata, and Pteris creticaWidely accepted in some places[70, 73, 74, 75, 76]
MethylationsBiomethylations (by As(III) (by As(III) S-adenosylmethionine methyltransferaseIs a reliable biological process of removing arsenic from aquatic mediums[70]
ReductionReduction of arsenate into arsenite by microorganisms via dissimilatory reduction mechanismShould be carried out in facultative anaerobe or strict anaerobe condition[70]
OxidationUsing heterotrophic bacteria and chemoautotrophic bacteria to oxidize arsenite into a less toxic arsenateShould be carried out in controlled environment[80, 81, 82, 83]

Table 4.

Characteristics of various methods for the removal of arsenic from aqueous system.

Such information should be taken into consideration in order to improve the current methods or develop new advanced methods. The best analytical methods for aresenic speciation are considered those, including chromatographic separations based on adsorption coupled with a sensitive detection system. Specific sorbents and exchange resins have been developed and applied recently for this purpose. Apart from the chromatographic and non-chromatographic methods for the arsenic species separation, simple and cost-effective electrochemical methods were developed recently based on the distinct As-species electrochemical properties [84].


6. Conclusion

This chapter on removal of arsenic - “a silent killer” in the environment by adsorption methods has been discussed. Moreover, recently the consumers have become very much conscious about the environment, renaissance of eco-friendly products and process, which has thus become also important now. Thus, revival of natural arsenic application on various areas and summary of earlier researches on standardization of its method of extraction, mordanting, process variables and even natural finishing, etc. have been elaborated in this chapter. Thus this part has become a unique comprehensive chapter for information on removal of ‘arsenic’ a silent killer in the environment by adsorption method. A brief review of the removal of arsenic ions from water using iron-based adsorbents has been presented. A few adsorbents discussed in this chapter include relative advantages and disadvantages of adsorbents used for the removal of arsenic from water have been mentioned. The mechanism of arsenic adsorption on iron-containing adsorbents was summarized. Overall, there exist significant progress and benefit on using adsorption process for removing arsenic species from groundwater in a practical way to make potable water accessible for the rural population.


Conflict of interest

There is no conflict of interest.


  1. 1.Zhegunov G., The Dual Nature of Life, The Frontiers Collection, Springer-Verlag Berlin Heidelberg, 1(300), 2012
  2. 2.Azarmi R. and Ashjaran A. “Type and application of some common surfactants” Journal of Chemical and Pharmaceutical Research, 7(2):632-640, 2015
  3. 3.Elsberry C.C., Belanger S. etal “Environmental Safety of the Use of Major Surfactant Classes in North America”, Critical Reviews in Environmental Science and Technology, 44(17): 2014
  4. 4.Purakayastha P.D., etal “Adsorbent selection for anionic surfactant removal from water”, Indian Journal of Chemical Technology, 12(281-284), 2005
  5. 5.Bagul V. R.; Shinde D. N,etal “Causes and Impacts of Water Pollution on Rivers in Maharashtra-A Review” , Research Journal of Chemical and Environmental Sciences, 3 [6] 2015
  6. 6.Tripathy D. B., Mishra A. eatal “Biodegradability of Laundry Detergent Surfactants”, Journal of Surfactants and Detergents, 5(130-136), 2015
  7. 7.Mathur N., Bhatnagar P., “Review of the Mutagenicity of Textile Dye Products” Universal Journal of Environmental Research and Technology, 2(1-18), 2012
  8. 8.ElsalamM.R.M.A. “Studies on the Use of Surface Active Agents for the Removal of Some Pollutants from Dilute Aqueous”, Hot Labs. Center- Atomic Energy, 2007
  9. 9.Bittton G., WileyJ. and sons “Wastewater microbiology” 3(63-65),1994. DOI: 10.1002/978047974704.ch5
  10. 10.Ratana, Padhi B.s.Polltution due to synthetic dyes toxicity and carcinogenicity studies and remediation”, International Jouranal of Enviornmental Sciences, 3(940-955), 2012
  11. 11.Mazumdar D., “Process evaluation and treatability study of wastewater in textile dyeing industry”, International Journal of Energy and Environment, 2(1053-1066), 2011
  12. 12.Thakur S., Chauhan M.S., “Treatment of waste water by electro coagulation” 5(104-110), 2016
  13. 13.Lavanya C., Dhankar R. etal “Degradation of toxic dyes: A Review”, International Journal of Current Microbiology and Applied Sciences, 3(186-199), 2014
  14. 14.Rangabhashiyam S., N. Anu, Nandagopal M.S.G., Selvaraju N., “Relevance of isotherm models in biosorption of pollutants by agricultural byproducts.”, Journal of Environmental Chemical Engineering, 2(398-414), 2014
  15. 15.C. G. Lee, P. J. J. Alvarez, A. Nam, et al., Effective removal of arsenate from wastewater using aluminium enriched ferric oxide-hydroxide recovered from authentic acid mine drainage J. Hazard. Mater., 2017, 325, 223-229
  16. 16.Symonds, M.R.E., Moussalli, A. A brief guide to model selection, multimodel inference and model averaging in behavioural ecology using Akaike’s information criterion. Behav Ecol Sociobiol 65, 13-21
  17. 17.MontoyaV.H., ServinJ.G., “Thermal Treatments and Activation Procedures used in the Preparation of Activated Carbons” Instituto Tecnológico de Aguascalientes México, 2(92), 2012
  18. 18.S. I. Siddiqui and S. A. Chaudhry, Iron oxide and its modified forms as an adsorbent for arsenic removal: A comprehensive recent advancement Process Saf. Environ. Prot., 2017, 111, 592-626
  19. 19.K. Jomova, Z. Jenisova, M. Feszterova, et al., Arsenic: toxicity, oxidative stress and human disease J. Appl. Toxicol., 2011, 31, 95-107
  20. 20.L. Fang, X. Y. Min, R. F. Kang, et al., A critical review on arsenic removal from water using iron-based adsorbents Sci. Total Environ., 2018, 639, 110-117
  21. 21.M. A. Hoque, W. G. Burgess and K. M. Ahmed, Itregation of aquifer geology, ground water flow and arsenic distribution in deltaic aquifers- a unifying concept Hydrol. Processes, 2017, 31, 2095-2109
  22. 22.S. V. Jadhav, E. Bringas, G. D. Yadav, et al., Arsenic and fluoride contaminated groundwaters: a review of current technologies for contaminants removal J. Environ. Manage., 2015, 162, 306-325
  23. 23.M. Singh, A. K. Singh, N. Srivastava, et al., Arsenic mobility in fluvial environment of the Ganga Plain, northern India Environ. Earth Sci., 2010, 59, 1703-1715
  24. 24.W. Baeyens, A. de Brauwere, N. Brion, et al., Arsenic speciation in the River Zenne, Belgium Sci. Total Environ., 2007, 384, 409-419
  25. 25.A. Barats, G. F’eraud, C. Potot, et al. Naturally dissolved arsenic concentrations in the Alpine/Mediterranean Var River watershed (France), Sci. Total Environ., 2014, 473, 422-436
  26. 26.M. Arain, T. Kazi, J. Baig, et al., Co-exposure of arsenic and cadmium through drinking water and tobacco smoking: Risk assessment on kidney dysfunctionFood Chem. Toxicol., 2009, 47, 242-248
  27. 27.Andjelkovic, S. Azari, M. Erkelens, et al., Bacterial iron-oxide nanowires from biofilm waste as a new adsorbent for the removal of arsenic from water† RSC Adv., 2017, 7, 3941-3948
  28. 28.V. Pallier, G. Feuillade-Cathalifaud, B. Serpaud, et al., Effect of organic matter on arsenic removal during coagulation/flocculation treatment J. Colloid Interface Sci., 2010, 342, 26-32
  29. 29.G. Ungureanu, S. Santos, R. Boaventura, et al., Effects of iron oxide on antimony(V) adsorption in natural soils: transmission electron microscopy and X-ray photoelectron spectroscopy measurements J. Environ. Manage., 2015, 151, 326-342
  30. 30.S. Maeda, S. Nakashima, T. Takeshita, and S. Higashi, “Bioac- cumulation of arsenic by freshwater algae and the application to the removal of inorganic arsenic from an aqueous phase. Part II. ByChlorella vulgarisisolated from arsenic-polluted
  31. 31.J. Yoon, G. Amy, J. Chung, et al., Occurrence of Perchlorate in Drinking Water and Seawater in South Korea Chemosphere, 2009, 77, 228-235
  32. 32.W. Driehaus and F. Dupont, A critical review on arsenic removal from water using iron-based adsorbents Eur. J. Water Qual., 2010, 36, 138-147
  33. 33.M. A. Pintor, B. R. C. Vieira, S. C. R. Santos, et al., Drinking Water Treatments for Arsenic and Manganese Removal and Health Risk Assessment in White Rock, Canada Sci. Total Environ., 2018, 642, 1075-1089
  34. 34.P. Qi and T. Pichler, Chemosphere, 2016, Volume 145, 55-60
  35. 35.J. Cantu, L. E. Gonzalez, J. Goodship, et al., Removal of Arsenic from water using synthetic Fe7S8 nanoparticles Chem. Eng. J., 2016, 290, 428-437
  36. 36.M. Podder and C. Majumder, Optimization of environmental conditions for the growth and bioaccumulation of As(III) and As(V) ions by growing Corynebacterium glutamicum MTCC 2745: inhibition kinetic study Spectrochim. Acta, Part A, 2016, 153, 298-314
  37. 37.M. C. Collivignarelli, M. Canato, S. Sorlini, et al., What Advanced Treatments Can Be Used to Minimize the Production of Sewage Sludge in WWTPs?Water Practice & Technology, 2016, 11, 115-126
  38. 38.M. K. Ghosh, G. E. J. Poinern, T. B. Issa, et al., Arsenic adsorption on goethite nanoparticles produced through hydrazine sulfate assisted synthesis method Korean J. Chem. Eng., 2012, 29, 95-102
  39. 39.S. Vasudevan and J. Lakshmi, Electrochemical removal of boron from water: Adsorption and thermodynamic studies Can. J. Chem. Eng., 2012, 90, 1017-1026
  40. 40.R. Chowdhury, Using adsorption and sulphide precipitation as the principal removal mechanisms of arsenic from a constructed wetland – a critical review Chem. Ecol., 2017, 33, 560-571
  41. 41.NANZHU LI , Ferrate as a New T ate as a New Treatment Chemical for Remo eatment Chemical for Removal of Effluent al of Effluent Organic Matter (E ganic Matter (EfOM) and Emer fOM) and Emerging Micr ging Micro-Pollutants in T ollutants in Treated Municipal Wastewater for Water Reuse, Montclair State University Upper Montclair, NJ 2017
  42. 42.M. C. Faria, R. S. Rosemberg, C. A. Bomfeti, et al., Removal of arsenic from water through adsorption onto metal oxide-coated material, Book,Applications of Adsorption and Ion Exchange Chromatography in Waste Water TreatmentVol. 15, pp 227-276, 2017
  43. 43.X. Sun, C. Hu, X. Hu, et al., Characterization and adsorption performance of Zr-doped akaganéite for efficient arsenic removal J. Chem. Technol. Biotechnol., 2013, 88, 629-635
  44. 44.W. Tang, Q. Li, S. Gao, et al.,Arsenic (III, V) removal from aqueous solution by ultrafine α-Fe2O3 nanoparticles synthesized from solvent thermal method. J. Hazard. Mater., 2011, 192, 131-138
  45. 45.H. Park, N. V. Myung, H. Jung, et al., Electrochemical synthesis of magnetic iron oxide nanoparticles with controlled size J. Nanopart. Res., 2009, 11, 1981-1989
  46. 46.Mohammad-Khah A, Ansari R Activated charcoal: preparation, characterization and applications: a review article. Int J Chem Tech Resour, 2009, 1:859-864
  47. 47.Ansari R, Sadegh M Application of activated carbon for removal of arsenic ions from aqueous solutions. E- J Chemistry, 2007, 4:103-108
  48. 48.Bansal RC, Donet JB, Stoeckli F, A review of active carbon, 1988, Marcel Dekker, New York
  49. 49.Kairvelu K, Thamaraiselvi K, Namazivayam C Removal of heavy metals from industrial wastewaters by adsorption onto activated carbon prepared from an agricultural solid waste. Bioresour Technol, 2001, 76:63-65
  50. 50.Srivastava S, Agrawal SB, Mondal MK, A review on progress of heavy metal removal using adsorbents of microbial and plant origin, Environ Sci Pollut, 2015, 22:15386-15415
  51. 51.Kairvelu K, Thamaraiselvi K, Namazivayam C, Removal of heavy metals from industrial wastewaters by adsorption onto activated carbon prepared from an agricultural solid waste, Bioresour Technol, 2001, 76:63-65
  52. 52.Lorenzen L, van Deventer JSJ, Land WM Factors affecting the mechanism of the adsorption of arsenic species on activated carbon, Miner Eng, 1995, 8:557-569
  53. 53.Li Z, Deng S, Yu G, Huang J, Lim VC As(V) and As(III) removal from water by a Ce–Ti oxide adsorbent: behavior and mechanism, J Chem Eng,2010, 161:106-113
  54. 54.Liu Z, Zhang FS, Sasai R, Arsenate removal from water using Fe3O4-loaded activated carbon prepared from waste biomass. J Chem Eng, 2010, 160:57-62
  55. 55.Pattanayak J, Mondal K, Mathew S, Lalvani SB, A parametric evaluation of the removal of As(V) and As(III) by carbon based adsorbents, Carbon, 2000, 38:589-596
  56. 56.Genc-Fuhrman TJC, McConchie D, Increasing the arsenate adsorption capacity of neutralized red mud (Bauxsol). J Colloid Interface Sci, 2004, 271:313-320
  57. 57.Shafique U, Ijaz A, Salman M, UzzamaW, Jamil N, Rehman R, Javaid A, Removal of arsenic from water using pine leaves. J Taiwan Inst Chem Engineers, 2012 43:256-263
  58. 58.Chuang CL, Fan M, Xu M, Brown RC, Sung S, Saha B, Huang BL, Adsorption of arsenic(V) by activated carbon prepared from oat hulls. Chemosphere, 2005 Chapter-21, Page no.-478-483
  59. 59.Chang QG, Lin W, Ying WC, Preparation of iron-impregnated granular activated carbon for arsenic removal from drinking water,J Hazard Mater, 2010,184:515-522
  60. 60.Tuna AOA, Ozdemir E, Simsek EB, Beker U, Removal of As(V) from aqueous solution by activated carbon-based hybrid adsorbents: impact of experimental conditions, J Chem Eng, 2013, 223:116-128
  61. 61.Lodeiro P, Kwan SM, Perez JT, Gonzalez LF, Gerente C, Andres Y, McKay G, Novel Fe loaded activated carbons with tailored properties for As(V) removal: adsorption study correlated with carbon surface chemistry, J Chem Eng, 2013, 215:105-112
  62. 62.Samsuri AW, Sadegh-Zadeh F, Seh-Bardan BJ, Adsorption of As(III) and As(V) by Fe coated biochars and biochars produced from empty fruit bunch and rice husk, J. Environ. Chem. Eng., 2013, 1: 981-988
  63. 63.Chammui Y, Sooksamiti P, Naksata W, Thiansem S, Arqueropanyo OA, Removal of arsenic from aqueous solution by adsorption on Leonardite, JChem Eng, 2014,240:202-210
  64. 64.Lunge S, Singh S, Sinha A, Magnetic iron oxide (Fe3O4) nanoparticles from tea waste for arsenic removal, Magn Mater, 2014, 356:21-31
  65. 65.Sigrist ME, Brusa L, Beldomenico HR, Dosso L, Tsendra OM, Gonzalez MB, Pieck CL, Vera CR, Influence of the iron content on the arsenic adsorption capacity of Fe/GAC adsorbents, J Environ Chem Eng, 2014, 2:927-934
  66. 66.Chen RZ, Zhang ZY, Yang N, Lei ZF, ChenN, Guo X, Zhao C, Sugiura N, Use of ferric-impregnated volcanic ash for arsenate(V) adsorption from contaminated water with various mineralization degrees, J Colloid Interface Sci, 2011, 353:542-548
  67. 67.Gerente C, Andres Y, McKay G, Le Cloirec P,Removal of arsenic(V) onto chitosan: from sorption mechanism explanation to dynamic water treatment process, J Chem Eng, 2010, 158:593-598
  68. 68.S. Mahimairaja, N. S. Bolan, D. C. Adriano, and B. Robinson, Arsenic contamination and its risk management in complex environmental settings, Advances in Agronomy, 2005, vol. 86, pp. 1– 82
  69. 69.C. Sullivan, M. Tyrer, C. R. Cheeseman, and N. J. D. Graham, Disposal of water treatment wastes containing arsenic, Science of the Total Environment, 2010, 408, 1770-1778
  70. 70.O. Atteia, E. D. C. Estrada, and H. Bertin, Soil flushing: the origin of efficiency variability, Review of Environment, Science and Biotechnology, 2013, 12, 379-389
  71. 71.A. A. L. S. Duarte, S. J. A. Cardoso, and A. J. Alcada, Emerging and innovative techniques for arsenic removal applied to a small water supply system, 2009, Sustainability, 1, 1288-1304
  72. 72.M. Koma’rek, A. Vaneˇk, and V. Ettler, Chemical stabilization of metals and arsenic in contaminated soils using oxides, Envi- ronmental Pollution, 2013, 172, 9-22
  73. 73.N. C. Mueller and B. Nowack, Nanoparticles for remediation: solving big problems with little particles, Elements, 6, 395-400
  74. 74.K.-R. Kim, B.-T. Lee, and K.-W. Kim, Arsenic stabilization in mine tailings using nano-sized magnetite and zero valent iron with the enhancement of mobility by surface coating, Journal of Geochemical Exploration, 2012, 113, 124-129
  75. 75.E. D. Leiva, C. D. P. Ra’mila, I. T. Vargas et al., Natural attenuation process via microbial oxidation of arsenic in a high Andean watershed, Science of the Total Environment, 2014, 466- 467, 490-502
  76. 76.E. K. Porter and P. J. Peterson, Arsenic accumulation by plants on mine waste (United Kingdom), Science of the Total Environment, 1975, 4, 365-371
  77. 77.M. I. Silva Gonzaga, J. A. Gonzaga Santos, and L. Q. Ma, Arsenic phytoextraction and hyperaccumulation by fern species, Scientia Agricola, 63, 1, 2006, 90-101, 2006
  78. 78.Q. Yang, S. Tu, G. Wang, X. Liao, and X. Yan, Effectiveness of applying arsenate reducing bacteria to enhance arsenic removal from polluted soils by Pteris vittata L, International Journal of Phytoremediation, 2012, 14,89-99
  79. 79.J. Xiong, W. Wang, H. Fan, L. Cai, and G. Wang, Arsenic resistant bacteria in mining wastes from Shangrao coal mine of China, Environmental Science and Technology, 2006, 1, 535– 540
  80. 80.H. M. Sehlin and E. B. Lindstrom, Oxidation and reduction of arsenic by Sulfolobus acidocaldarius strain BC, FEMS Microbiology Letters, 1992, 93, 87-92
  81. 81.D. Lie’vremont, P. N. Bertin, and M.-C. Lett, Arsenic in contaminated waters: biogeochemical cycle, microbial metabolism and biotreatment processes, Biochimie, 2009, 91, 1229-1237
  82. 82.D. Muller, D. Lie’vremont, D. D. Simeonova, J.-C. Hubert, and M.-C. Lett, Arsenite oxidase aox genes from a metal-resistant 𝛽-proteobacterium, Journal of Bacteriology, 2003, 185, 135-141
  83. 83.K. Chitpirom, S. Tanasupawat, A. Akaracharanya et al., Coma- monas terrae sp. nov., an arsenite-oxidizing bacterium isolated from agricultural soil in Thailand, Journal of General and Applied Microbiology, 2012, 58, 245-251
  84. 84.Margarita Stoytcheva and Roumen Zlatev (July 25th 2018). Introductory Chapter: Arsenic, Arsenic - Analytical and Toxicological Studies, Margarita Stoytcheva and Roumen Zlatev, IntechOpen

Written By

Ashok Kumar, Kaman Singh, Utkarsh Dixit, Rayees Ahmad Bhat and Satya Prakash Gupta

Submitted: June 11th, 2021Reviewed: June 19th, 2021Published: September 8th, 2021