Antimony adsorption on kaolinite in the presence of competitive anions

Antimony (Sb) emissions to the environment are increasing, and there is a dearth of knowledge regarding Sb fate and behavior in natural systems. In natural systems, the presence of competitive anions may compete with Sb for adsorption sites on mineral surfaces, hence increasing its potential bioavailability. Accordingly, the adsorption of Sb(III) on kaolinite was investigated in the presence of competitive anions. Kinetic studies suggest that adsorption reaction of Sb(III) on kaolinite is rapid initially and becoming slow after 12 h both in binary Sb(III)–kaolinite system and in ternary Sb(III)-competitive anion–kaolinite system. The presence of PO₄ ^3? has a much stronger and more obvious promotive effect on the adsorption of Sb(III) on kaolinite compared with the other two anions. The adsorption data of Sb(III) on kaolinite in the absence and presence of competitive anions at three temperatures were successfully modeled using Langmuir (r ² > 0.95) and Freundlich (r ² > 0.95) isotherms. Accompanied the adsorption of Sb(III) on kaolinite, significant oxidation of Sb(III) to Sb(V) had occurred under the experimental conditions used in this study. The presence of kaolinite which has a larger specific surface area could increase the contact area between the adsorbed Sb(III) and oxygen in the bulk solution, which promoted the oxidation rate of Sb(III) to Sb(V).     

Synthetic Mn3+-kyanite and viridine, (Al2-xMn x 3+ ) SiO5, in the system Al2O3-MnO-MnO2-SiO2

Experiments on the join Al₂SiO₅-“Mn₂SiO₅” of the system Al₂O₃-SiO₂-MnO-MnO₂ in the pressure/temperature range 10–20 kb/900–1050° C with gem quality andalusite, Mn₂O₃, and high purity SiO₂ as starting materials and using /_O2-buffer techniques to preserve the Mn³⁺ oxidation state had following results: At 20 kb/1000°C orange-yellow kyanite mixed crystals are formed. The kyanite solid solubility is limited at about (Al_1.88Mn _0.12 ³⁺ )SiO₅ and, thus, equals approximately that on the join Al₂SiO₅-“Fe₂SiO₅” (Langer and Frentrup, 1973) indicating that there is no Jahn-Teller stabilisation of Mn³⁺ in the kyanite matrix. 5 mole % substitution causes the kyanite lattice constants a _o, b _o, c _o, and V _o to increase by 0.015, 0.009, 0.014 Å, and 1.6 ų, resp., while α, β, γ, remain unchanged. Between 10 and 18 kb/900°C, Mn³⁺-substituted, strongly pleochroitic (emeraldgreen-yellow) andalusite_ss (viridine) was obtained. At 15 kb/900°C, the viridine compositional range is about (Al_1.86Mn _0.14 ³⁺ )SiO₅-(Al_1.56Mn _0,44 ³⁺ )SiO₅. Thus, Al→Mn³⁺ substitutional degrees are appreciably higher in andalusite than in kyanite, proving a strong Jahn-Teller effect of Mn³⁺ in the andalusite structure, which stabilises this structure type at the expense of kyanite and sillimanite and, thus, enlarges its PT-stability range extremely. 17 mole % substitution cause the andalusite constants a _o, b _o, c _o, and V _o to increase by 0.118, 0.029, 0.047 Å and 9.4 ų, resp. At “Mn₂SiO₅”-contents smaller than about 7 mole %, viridine coexists with Mn-poor kyanite. At “Mn₂SiO₅”-concentrations higher than the maximum kyanite or viridine miscibility, braunite (tetragonal, ideal formula Mn²⁺Mn³⁺[O₈/Si0₄]), pyrolusite and SiO₂ were found to coexist with the Mn³⁺-saturated ky _ss or and _ss, respectively. In both cases, braunites were Al-substituted (about 1 Al for 1 Mn³⁺). Pure synthetic braunites had the lattice constants a _o 9.425, c _o, 18.700 Å, V _o 1661.1 ų (ideal compn.) and a _o 9.374, c _o 18.593 ų, V _o 1633.6 ų (1 Al for 1 Mn³⁺). Stable coexistence of the Mn²⁺-bearing phase braunite with the Mn⁴⁺-bearing phase pyrolusite was proved by runs in the limiting system MnO-MnO₂-SiO₂.     

Modeling transport of arsenic through modified granular natural siderite filters for arsenic removal

Groundwater arsenic(As)contamination is a hot issue,which is severe health concern worldwide.Recently,many Fe-based adsorbents have been used for As removal from solutions.Modified granular natural siderite(MGNS),a special hybrid Fe(II)/Fe(III)system,had higher adsorption capacity for As(III)than As(V),but the feasibility of its application in treating high-As groundwater is still unclear.In combination with transport modeling,laboratory column studies and field pilot tests were performed to reveal both mechanisms and factors controlling As removal by MGNS-filled filters.Results show that weakly acid pH and discontinuous treatment enhanced As(Ⅲ)removal,with a throughput of 8700 bed volumes(BV)of 1.0 mg/L As(Ⅲ)water at breakthrough of 10 μg/L As at pH 6.Influent HCO_3~-inhibited As removal by the filters.Iron mineral species,SEM and XRD patterns of As-loading MGNS show that the important process contributing to high As(Ⅲ)removal was the mineral transformation from siderite to goethite in the filter.The homogeneous surface diffusion modeling(HSDM)shows that competition between As(III)and HCO_3~-with adsorption sites on MGNS was negligible.The inhibition of HCO_3~-on As(Ⅲ)removal was connected to inhibition of siderite dissolution and mineral transformation.Arsenic loadings were lower in field pilot tests than those in the laboratory experiments,showing that high concentrations of coexisting anions(especially HCO_3~-and SiO_4~(4-)),high pH,low EBCT,and low groundwater temperature decreased As removal.It was suggested that acidification and aeration of highAs groundwater and discontinuous treatment would improve the MGNS filter performance of As removal from real high-As groundwater.     

Nonlinear kinetic analysis of phenol adsorption onto peat soil

Phenolic compounds are considered as a serious organic pollutant containing in many industrial effluents particularly vulnerable when the plant discharge is disposed on land. In the present study, the phenol removal potential of peat soil as adsorption media was investigated as the adsorption process are gaining popular for polishing treatment of toxic materials in industrial wastewater. Batch experiments were performed in the laboratory to determine the adsorption isotherms of initial concentrations for 5, 8, 10, 15, and 20 mg/L and predetermined quantity of peat soil with size ranges between 425 and 200 μm poured into different containers. The effects of various parameters like initial phenol concentration, adsorbent quantity, pH, and contact time were also investigated. From experimental results, it was found that 42 % of phenol removal took place with optimized initial phenol concentration of 10 mg/L, adsorbent dose of 200 g/L, solution pH 6.0 for the equilibrium contact time of 6 h. The result exhibits that pseudo-first-order (R ² = 0.99) and Langmuir isotherm models are fitted reasonably (R ² = 0.91). Adams–Bohart, Thomas, Yoon–Nelson, and Wolborska models were also investigated to the column experimental data of different bed heights to predict the breakthrough curves and to determine the kinetic coefficient of the models using nonlinear regression analysis. It was found that the Thomas model is the best fitted model to predict the experimental breakthrough curves with the highest coefficient of determination, R ² = 0.99 and lowest root mean square error and mean absolute performance error values.     

Chemical characteristics of coastal rainwater from Puducherry to Neithavasal,Southeastern coast of India

The chemistry of the rainwater indirectly reflects the composition of the ions in the atmosphere. The study of the rainwater gains its own importance as it forms the basis for the agricultural, domestic and drinking water. Twelve rainwater samples were collected along the southeastern coast of India during southwest monsoon. The samples were analyzed for the major anions (Cl^?, SO₄ ^2?, PO₄ ^3? and HCO₃ ^?) and cations (Na⁺, K⁺, Ca²⁺ and Mg²⁺). The majority of the samples reflect acidic pH. The general dominance of the cations is in the order of Na⁺ > Ca²⁺ > K⁺ > Mg²⁺ and that of anions is HCO₃ ^? > Cl^? > SO₄ ^2? > PO₄ ^3?. The water is classified as calcium bicarbonate to sodium bicarbonate type. The decrease of pH value also increases the pCO₂. In order to study the impact of acidic and alkaline species on rainwater, correlation coefficients were determined for establishing the relationship between different ions. Good correlation was established between cations, and sulfate has no correlation with other ions and pH. Factor analysis reveals that land use pattern, marine source and methanogenesis from the tidal influenced mangroves play a major role in determining the rainwater chemistry of the region.     

Removal of arsenic and iron from mine-tailing leachate using chitosan hydrogels synthesized by gamma radiation

Mine residue and leachate were sampled from an acid mine drainage site near Arroyo San Pedro, which is one of the oldest abandoned mine districts in San Luis Potosi, Mexico, and characterized by X-ray diffraction and inductively coupled plasma-optical emission spectroscopy, confirming the presence of Fe, As, and SO₄ ^2?. To address this problem, chitosan network (net-CS) and chitosan network-N-vinylcaprolactam/N–N-dimethylacrylamide (net-CS)-g-NVCL/DMAAm hydrogels were synthesized and used as adsorbents of the different ions present in the aforementioned leachate by batch equilibrium procedure. Kinetics, isotherms, and ions dissolved in leachate were evaluated. The gels showed the highest adsorption capacity for As and Fe ions. The adsorption capacity of the net-CS hydrogels for As (V) and Fe(III) was 0.786 and 76.85 mg/g, respectively, attained after 50 h. The surface of the hydrogels was investigated by scanning electron microscopy and Fourier transform infrared spectroscopy, before and after the adsorption process, where the presence of a bond between the hydrogels and heavy metals ions, which is commonly observed in organic groups, was observed. In addition, Freundlich and Langmuir adsorption isotherms constants were determined for the As and Fe ions, and it was found that the Freundlich isotherm, with a first-order pseudo model, better fitted the adsorption process, indicating heterogeneous sorption, and the retention process occurred by chemisorption. The results from the Geochemist´s Workbench (GWB) software program revealed that arsenates, such as H₃AsO₄, H₂AsO₄ ^?, as well as Fe⁺⁺, FeSO₄(aq) and FeOH⁺ were the common aqueous species found in the leachate at pH = 2.9.     

Assessment of groundwater quality for irrigation purposes and identification of hydrogeochemical evolution mechanisms in Pengyang County, China

Groundwater is an important water source for agricultural irrigation in Penyang County. Some traditional methods such as irrigation coefficient, sodium adsorption ratio, total alkalinity, total salinity and total dissolved solids were employed to assess groundwater quality in this area. In addition, an improved technique for order preference by similarity to ideal solution model was applied for comprehensive assessment. The origin of major ions and groundwater hydrogeochemical evolution was also discussed. Groundwater in Penyang County contains relative concentrations of dominant constituents in the following order: Na⁺ > Ca²⁺ > Mg²⁺ > K⁺ for cations and HCO₃ ^? > SO₄ ^2? > Cl^? > CO₃ ^2? for anions. Groundwater quality is largely excellent and/or good, suggesting general suitability for agricultural use. Calcite and dolomite are found saturated in groundwater and thus tend to precipitate out, while halite, fluorite and gypsum are unsaturated and will dissolve into groundwater during flow. Groundwater in the study area is weathering-dominated, and mineral weathering (carbonate and silicate minerals) and ion exchange are the most important factors controlling groundwater chemistry.     

Clicking graphene oxide and Fe3O4 nanoparticles together: an efficient adsorbent to remove dyes from aqueous solutions

Nanohybrid of graphene oxide (GO) and azide-modified Fe₃O₄ nanoparticles (NPs) were fabricated using click reaction. First, Fe₃O₄ NPs were modified by 3-azidopropionic acid. Then, click-coupling of azide-modified Fe₃O₄ NPs with alkyne-functionalized GO was carried out in the presence of CuSO₄·5H₂O and sodium l-ascorbate at room temperature. The attachment of Fe₃O₄ NPs onto the graphene nanosheets was confirmed by Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy, thermogravimetric analysis, energy dispersive X-ray spectrometry and X-ray diffraction spectrometry. As the FTIR spectroscopy and energy dispersive X-ray spectrometry analysis showed, the final magnetic graphene nanosheets were also reduced by sodium ascorbate which is a merit for click-coupling reactions. The specific saturation magnetization of the Fe₃O₄-clicked GO was 44.3 emu g^?1. The synthesized hybrid was used in the adsorption of methylene blue and congo red (CR). The adsorption capacities in the studied concentration range were 109.5 and 98.8 mg g^?1 for methylene blue and CR, respectively.     

Synthesis and physical properties of piemontite Ca2Al3-pMn p 3+ (Si2O7/SiO4/O/OH)

Mn³⁺-bearing piemontites and orthozoisites, Ca₂(Al_3-pMn³⁺ _p)-(Si₂O₇/SiO₄/O/OH), have been synthesized on the join Cz (p = 0.0)-Pm (p = 3.0) of the system CaO-Al₂O₃-(MnO·MnO₂)-SiO₂-H₂O atP = 15 kb,T= 800 °C, and \(f_{O_2 } \) of the Mn₂O₃/MnO₂ buffer. Pure Al-Mn³⁺-piemontites were obtained with 0.5≦p≦1.75, whereas atp=0.25 Mn³⁺-bearing orthozoisite (thulite) formed as single phase product. The limit of piemontite solid solubility is found near p=1.9 at the above conditions. Withp>1.9, the maximum piemontite coexisted with a new high pressure phase CMS-X1, a Ca-bearing braunite (Mn _0.2 ²⁺ Ca_0.8)Mn ₆ ³⁺ O₈(SiO₄), and quartz. Al-Mn³⁺-piemontite lattice constants (LC),b ₀,c ₀,V ₀, increase with increasingp:

Electron paramagnetic resonance study of iron(III) and manganese(II) in the glassy and crystalline environments of synthetic fayalite and tephroite

Crystals of the olivine minerals, tephroite (Mn₂SiO₄) and fayalite (Fe₂SiO₄) containing manganese(II) and iron (II and trace of III), respectively, were synthesized. Glasses were prepared from these crystalline materials by a splat-quench technique. Measurement of electron paramagnetic resonance (EPR) of all these powdered samples at room temperature show that the g-factors of Mn²⁺ in both glassy and crystalline environments (g_eff = 2.004) are the same, although the EPR linewidths (for glass, ΔH_pp = 200 G; for crystals ΔH_pp = 287 G) suggest less clustering of paramagnetic Mn²⁺ ions in the glass. Mn²⁺ probably occupies a distorted octahedral site in the tephroite crystal structure, although a four-fold coordination is suggested from other spectroscopic investigation on this glass. The EPR parameters of Fe³⁺ in synthetic fayalite glass (g_eff = 2.01 and 6.00; ΔH_pp=150 and 1375 G, respectively, for the high and low field resonances) and powdered crystals (g_eff = 3.31 and ΔH_pp = 900 G) indicated that Fe³⁺ ion in the crystals, is probably located in a distorted tetragonal site M2 and an axial environment has been proposed in the glassy system.     

Removal of lead (II) from synthetic and batteries wastewater using agricultural residues in batch/column mode

The present article explores the ability of five different combinations of two adsorbents (Arachis hypogea shell powder and Eucalyptus cameldulensis saw dust) to remove Pb(II) from synthetic and lead acid batteries wastewater through batch and column mode. The effects of solution pH, adsorbent dose, initial Pb(II) concentration and contact time were investigated with synthetic solutions in batch mode. The Fourier transform infrared spectroscopy study revealed that carboxyl and hydroxyl functional groups were mostly responsible for the removal of Pb(II) ions from test solutions. The kinetic data were found to follow pseudo-second-order model with correlation coefficient of 0.99. Among Freundlich and Langmuir adsorption models, the Langmuir model provided the best fit to the equilibrium data with maximum adsorption capacity of 270.2 mg g^?1. Column studies were carried out using lead battery wastewater at different flow rates and bed depths. Two kinetic models, viz. Thomas and Bed depth service time model, were applied to predict the breakthrough curves and breakthrough service time. The Pb(II) uptake capacity (q _e = 540.41 mg g^?1) was obtained using bed depth of 35 cm and a flow rate of 1.0 mL min^?1 at 6.0 pH. The results from this study showed that adsorption capacity of agricultural residues in different combinations is much better than reported by other authors, authenticating that the prepared biosorbents have potential in remediation of Pb-contaminated waters.     

Removal of arsenate from aqueous media by magnetic chitosan resin immobilized with molybdate oxoanions

Chitosan was cross-linked using glutaraldehyde in the presence of magnetite. The resin obtained was chemically modified through the reaction with tetraethylenepentamine ligand. The obtained resin was loaded with Mo(VI) and investigated. The adsorption characteristics of the obtained resin toward As(V) at different experimental conditions were investigated by means of batch and column methods. The resin showed high affinity and fast kinetics for the adsorption of As(V) where an uptake value of 1.30 mmol g^?1 was reported in 6 min at 25 °C. Various parameters such as pH, agitation time, As(V) concentration and temperature had been studied. The kinetics and thermodynamic behavior of the adsorption reaction were defined. These data indicated an endothermic and spontaneous adsorption process and kinetically followed pseudo-second-order model, Fickian diffusion low and Elovich equation. Breakthrough curves for the removal of As(V) were studied at different flow rates and bed heights. The critical bed height for the studied resin column was found to be 0.656 cm at flow rate of 4 mL min^?1. The mechanism of interaction between As(V) and resin’s active sites was discussed. Regeneration and durability of the loaded resin toward the successive cycles were also clarified.     

Synthesis of Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>-loaded porous carbons developed from rice husk for removal of arsenate from aqueous solution

A simple one-step synthetic approach using rice husk has been developed to prepare magnetic Fe₃O₄-loaded porous carbons composite (MRH) for removal of arsenate (As(V)). The characteristics of adsorbent were evaluated by transmission electron microscope, scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller analysis, and thermogravimetric analysis. On account of the combined advantages of rice husk carbons and Fe₃O₄ nanoparticles, the synthesized MRH composites showed excellent adsorption efficiency for aqueous As(V). The removal of As(V) by the MRH was studied as a function of contact time, initial concentration of As(V), and media pH. The adsorption kinetics of As(V) exhibited a rapid sorption dynamics by a pseudo-second-order kinetic model, implying the mechanism of chemisorption. The adsorption data of As(V) were fitted well to the Langmuir isotherm model, and the maximum uptake amount (q _m ) was calculated as 4.33 mg g^?1. The successive regeneration and reuse studies showed that the MRH kept the sorption efficiencies over five cycles. The obtained results demonstrate that the MRH can be utilized as an efficient and low-cost adsorbent for removal of As(V) from aqueous solutions.     

Adsorption of hexavalent chromium onto activated carbon derived from <Emphasis Type="Italic">Leucaena leucocephala</Emphasis> waste sawdust: kinetics,equilibrium and thermodynamics

The adsorptive removal of Cr(VI) was studied using activated carbon derived from Leucaena leucocephala (ACLL). The physico-chemical properties of ACLL were determined using proximate analysis and N₂ BET surface area analysis. The N₂ BET surface area of ACLL was determined to be 1131 m² g^?1. The point of zero charge (pH_pzc) of 5.42 indicated that ACLL surface was positively charged for pH below the pH_PZC, attracting anions. The effect of experimental operating parameters such as time of contact, ACLL dose, pH, initial concentration and temperature was investigated. The optimum values of parameters such as concentration of 100 mg L^?1, 300 mg of ACLL dose, time of contact of 60 min, pH of 4 indicated the maximum Cr(VI) uptake of 13.85 mg g^?1. The pseudo-second-order kinetic model best fitted with the Cr(VI) adsorption data. Adsorptive removal of Cr(VI) onto ACLL satisfactorily fitted in the order of Redlich–Peterson > Freundlich > Langmuir > Temkin adsorption isotherm model. The thermodynamic parameters showed the adsorption of Cr(VI) onto ACLL was an endothermic and spontaneously occurred process.     

Groundwater appraisal of Dhekiajuli,Assam, India: an insight of agricultural suitability and arsenic enrichment

The present work is an effort to develop an appraisal of the hydrogeochemical regime for the aquifers of Dhekiajuli, Sonitpur district, Assam, which is imperative considering: (i) excessive use of groundwater for irrigation; (ii) reported high arsenic (As) contamination; (iii) application of fertilizer is an inevitable process undergoing in this region to achieve higher yield owing to deteriorating water quality; and (iv) study area being the location of many tea estates of Assam, that export tea in many foreign countries. The highest As concentration of 44.39 µg/L was detected in this study (Bachasimalu and Sitalmari region), implying high As-contaminated aquifers being used for drinking and irrigation purposes in the area. The relative abundance pattern of major cations and anions was in the order of Na⁺ > Mg²⁺ > Ca²⁺ > K⁺ and HCO₃ ^? > Cl^? > SO₄ ^2?, respectively. Majority of the samples belong to Na⁺–K⁺–Cl^?–HCO₃ ^? and mixed water type. Closer inspection of Piper plot reveals that a higher As value (>40 µg/L) was prevalent in HCO₃ ^? water type. Results of hydrogeochemical plots suggest silicate and carbonate weathering, ion exchange and anthropogenic activities to be the dominant processes governing groundwater contamination, including As which is further supported from PCA loadings. The Singri area to the east of the affected areas and adjacent to the Brahmaputra River has oxic aquifers owing to the absence of mass deposition of younger sediments, while reducing conditions prevails in the Bachasimalu and Sitalmari region. High positive correlation between As and Fe (r = 0.83**) and a negative correlation between ORP and Fe (r = ?0.68**) further add that Fe (hydr)oxides are the direct source of As release in the affected region, the mechanism being reductive hydrolysis of such (hydr)oxides. The study implies that although groundwater is suitable for irrigation use, there is a high probability of As getting into the food chain through tea and other edible plants irrigated with As-contaminated water; thus, the area has a maximum probability of facing health hazards caused by As-contaminated groundwater.     

Minerals of the viridine hornfels from Darmstadt,Germany

Viridine containing the highest amounts of Mn₂O₃ detected thus far (up to 20.5 mol % “Mn₂SiO₅”) coexists in a metasedimentary hornfels with spessartine, Mn-phlogopite (mangan-ophyllite), Mn-phengite (alurgite), hematite, quartz and probably some primary braunite. In layers poorer in viridine spessartine is absent but piemontite appears as an additional phase. Microprobe analyses of all these phases are presented which indicate very strong fractionation of Mg and Mn in coexisting phlogopite and garnet, and of Fe and Mn in coexisting hematite and braunite. Sericitic aggregates consisting of phengitic muscovite and braunite are interpreted as retrograde alteration products of viridine, but might partly be pinitic alterations of a former Mg-rich cordierite. Due to the occurrence of the assemblage spessartine-viridine-quartz Mn-cordierite cannot have been a stable phase prior to retrograde alterations. In general the stability field of viridine is extended towards higher temperatures as compared to that of pure andalusite, Al₂SiO₅. Due to the coexistence of phlogopite and muscovite (phengite) the temperature of contact metamorphism cannot have exceeded some 550°–650° C depending on the prevailing water pressure.     

Removal of lead(II) from aqueous stream by hydrophilic modified kapok fiber using the Fenton reaction

A hydrophilic kapok fiber was prepared by a chemical process of the Fenton reaction and used as an adsorbent to remove Pb(II) from aqueous solution. The effects of experimental parameters including pH, contact time, Pb(II) concentration, and coexisting heavy metals were estimated as well as evaluated. The optimum concentrations of FeSO₄ and H₂O₂ for the Fenton reaction-modified kapok fiber (FRKF) were 0.5 mol L^?1 and 1 mol L^?1, respectively. The adsorption kinetic models and isotherm equations of Langmuir and Freundlich were conducted to identify the most optimum adsorption rate and adsorption capacity of Pb(II) on FRKF. The FRKF displayed an excellent adsorption rate for Pb(II) in single metal solution with the maximum adsorption capacity of 94.41?±?7.56 mg g^?1 at pH 6.0. Moreover, the FRKE still maintained its adsorption advantage of Pb(II) in the mixed metal solution. The FRKF exhibited a considerable potential in removal of metal content in wastewater streams.     

Hydrogeochemistry of coal mine water of North Karanpura coalfields,India: implication for solute acquisition processes,dissolved fluxes and water quality assessment

Mine water samples collected from different mines of the North Karanpura coalfields were analysed for pH, electrical conductivity, total dissolved solids (TDS), total hardness (TH), major anions, cations and trace metals to evaluate mine water geochemistry and assess solute acquisition processes, dissolved fluxes and its suitability for domestic, industrial and irrigation uses. Mine water samples are mildly acidic to alkaline in nature. The TDS ranged from 185 to 1343 mg L^?1 with an average of 601 mg L^?1. Ca²⁺ and Mg²⁺ are the dominant cations, while SO₄ ^2? and HCO₃ ^? are the dominant anions. A high concentration of SO₄ ^2? and a low HCO₃ ^?/(HCO₃ ^? + SO₄ ^2?) ratio (<0.50) in the majority of the water samples suggest that either sulphide oxidation or reactions involving both carbonic acid weathering and sulphide oxidation control solute acquisition processes. The mine water is undersaturated with respect to gypsum, halite, anhydrite, fluorite, aluminium hydroxide, alunite, amorphous silica and oversaturated with respect to goethite, ferrihydrite, quartz. About 40% of the mine water samples are oversaturated with respect to calcite, dolomite and jarosite. The water quality assessment shows that the coal mine water is not suitable for direct use for drinking and domestic purposes and needs treatment before such utilization. TDS, TH, F^?, SO₄ ^2?, Fe, Mn, Ni and Al are identified as the major objectionable parameters in these waters for drinking. The coal mine water is of good to suitable category for irrigation use. The mines of North Karanpura coalfield annually discharge 22.35 × 10⁶ m³ of water and 18.50 × 10³ tonnes of solute loads into nearby waterways.     

Spatial variability of groundwater quality and its suitability for drinking and irrigation in the Amik Plain (South Turkey)

In this study, it is determined physicochemical properties of the groundwater and the spatial variability of physicochemical properties of the groundwater in the Amik plain and as well as assess its suitability for drinking and irrigation. A total 92 groundwater samples were collected from drilled well in June 2012. In addition, the 42 of 92 drilled wells were also sampled in September 2012 to evaluate the changes of groundwater properties. According to t test values, the mean Ca²⁺, SO₄ ^2?, Mg²⁺ and TH values in the June period were significantly lower than those of the September period. On the other hand, the mean (CO ₃ ^2?  + HCO₃ ^?) and RSC and MR values in the June period were significantly higher than those of the September period. The order of relative abundance of major cations in the groundwater (in mg L^?1) is in order Na⁺ > Mg²⁺ > Ca²⁺ > K⁺. The order of the anions abundance (mg L^?1) is SO₄ ^2? > Cl^? > HCO₃ ^? > CO₃ ^2? in this research. Log and square-root transformation were carried out for the most of the water properties before the calculation of semivariance. The nugget ratio showed all the variables were strongly spatial dependent except for K⁺ and Mg²⁺ and (CO₃ ^2? + HCO₃ ^?) which showed moderate spatial dependence (ratio ranging from 28 to 49.9 %). Spatial distribution analysis of groundwater quality indicated that The EC, TDS values and Na and Cl^? contents which is important water quality parameters increase from northern towards southern. The total hardness values increase also from northwestern towards southwestern.     

Effects of cations and anions on iron and manganese sorption and desorption capacity in calcareous soils from Iran

This study investigated the effect of cations and anions on the sorption and desorption of iron (Fe) and manganese (Mn) in six surface calcareous soil samples from Western Iran. Six 10 mM electrolyte background solutions were used in the study, i.e., KCl, KNO₃, KH₂PO₄, Ca(NO₃)₂, NaNO₃, and NH₄NO₃. NH₄NO₃ and NaNO₃ increased the soil retention of Fe and Mn, whereas Ca(NO₃)₂ decreased the soil retention of Fe and Mn. Iron and Mn sorption was decreased by NO₃ ^? compared with H₂PO₄ ^? or Cl^?. The Freundlich equation adequately described Fe and Mn adsorption, with all background electrolytes. The Freundlich distribution coefficient (K _F) decreased in the order H₂PO₄ ^? > Cl^? > NO₃ ^? for Mn and H₂PO₄ ^? > NO₃ ^? > Cl^? for Fe. The highest sorption reversibility was for Fe and Mn in competition with a Ca²⁺ background, indicating the high mobility of these two cations. A MINTEQ speciation solubility model showed that Fe and Mn speciation was considerably affected by the electrolyte background used. Saturation indices indicated that all ion background solutions were saturated with respect to siderite and vivianite at low and high Fe concentrations. All ion background solutions were saturated with respect to MnCO_3(am), MnHPO₄, and rhodochrosite at low and high Mn concentrations. The hysteresis indices (HI) obtained for the different ion backgrounds were regressed on soil properties indicating that silt, clay, sand, and electrical conductivity (EC) were the most important soil properties influencing Fe adsorption, while cation exchange capacity (CEC), organic matter (OM), and Mn-DTPA affected Mn adsorption in these soils.