Renewable-based treatment solution of Reactive Blue 21 dye on fly ash as low-cost and sustainable adsorbent.

This study investigated the removal of Reactive Blue 21 (RB 21) dye from aqueous solutions by adsorption, evaluating the waste fly ash (FA). The effects of the parameters, such as initial dye concentration (100-750 mg/L), initial pH (2.0-8.0), adsorbent dose (1.0-4.0 g/L), and temperature (298-323 K) on the adsorption process were investigated. The optimum initial pH value was 2.0 for the highest RB21 dye removal (75.2 mg/g). At optimized conditions (pH 2.0, an adsorbent dosage of 1.0 g/L, a dye concentration of 750 mg/L, and an equilibrium time of 72 h), the highest adsorption capacity was found to be 105.2 mg/g. Moreover, the results of the kinetic studies fitted the pseudo-second-order kinetic model. Equilibrium data were best represented by the Langmuir isotherm model, with a maximum monolayer adsorption capacity of 103.41 mg/g at 323 K. ΔGads0 values were negative and varied from 11.64 to 9.50 kJ/mol in the temperature range of 298-323 K, the values of enthalpy (ΔHadso) and entropy (ΔSadso) of thermodynamics parameters were calculated as 37.62 kJ/mol and 86.67 J/mol K, respectively, indicating that this process was endothermic. Furthermore, the adsorbent costs for powdered activated carbon (PAC) and FA to remove 1 kg of RB 21 dye from aqueous solutions are calculated as 2.52 U.S. $ and 0.34 U.S. $, respectively. It is seen that the cost of FA is approximately 7.4 times lower than PAC. The results showed that FA, a low-cost industrial waste, was promising for the adsorption of RB 21 from aqueous solutions.

Carbonaceous CoCr LDH nanocomposite as a light-responsive sonocatalyst for treatment of a plasticizer-containing water.

The carbonous-based nanocomposites of CoCr layered double hydroxide (LDH) with graphene oxide (GO) and reduced graphene oxide (rGO) were prepared. The successful synthesis of the CoCr LDH in hydrotalcite crystalline structure was deduced from the pattern obtained from X-ray diffraction, and the chemical composition of its surface was checked by X-ray photoelectron spectroscopy. The prosperous decorating of LDH on the sheets of rGO and GO was authenticated by the energy dispersive X-ray spectroscopy analysis and micrographs of scanning electron and transmission electron microscopy. The photo-assisted sonocatalytic activity of the prepared nanocomposites was appraised for the decomposition of dimethyl phthalate (DMP) as a plasticizer. The highest decomposition efficiency of 100% was obtained in the existence of CoCr LDH/rGO nanocomposite (0.5 g/L) during 20 min of reaction time via photo-assisted sonocatalysis. The rGO improved the catalytic activity of the CoCr LDH by increasing the specific surface area from 1.2 m2/g to 4.5 m2/g and reducing the band gap from 1.7 eV to 1.3 eV. Moreover, the results of the colony-forming unit method endorsed antibacterial property improvement of the CoCr LDH via hybridizing with rGO. The results of this research provide an optimistic perspective for applying carbonous-based nanocomposites of CoCr LDH as a novel catalyst with antibacterial properties in photo-assisted sonocatalytic processes.

Identifying Geogenic and Anthropogenic Aluminum Pollution on Different Spatial Distributions and Removal of Natural Waters and Soil in Çanakkale, Turkey.

The Çanakkale-Kirazli region (Turkey) is enriched with minerals, especially aluminum (Al), which dangerously get transported into aquatic media due to several mining and geological activities in recent years. In this study, Al and other potentially toxic metals (PTMs) including B, Ba, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Si, and Zn, in both water and soil samples, were measured for quality determination. Selected metals were also analyzed by the enrichment factor (EF), the geoaccumulation index (I geo), the contamination factor (CF), and the pollution load index (PLI) to evaluate both water and soil pollution geogenically or anthropogenically. Also, the metals were clustered to support the pollution source with Pearson's correlation, principal component analysis (PCA), and hierarchical cluster analysis (HCA). Forty-five natural water samples and 12 soil samples were collected spatially. To perform pollution assessment, two fundamental treatment processes to remove Al pollution from the sample including the highest Al concentration (38.38 mg/L) in water were applied: (1) precipitation with pH adjustment and (2) removal with ion exchange. The pH values of water samples were changed in the range of 3-9 to test the dissolution of Al. The results demonstrated that the study area was mostly under the influence of geogenic aluminum pollution.

Tuned CuCr layered double hydroxide/carbon-based nanocomposites inducing sonophotocatalytic degradation of dimethyl phthalate.

This study is the first to explore the possibility of utilizing CuCr LDH decorated on reduced graphene oxide (rGO) and graphene oxide (GO) as sonophotocatalysts for the degradation of dimethyl phthalate (DMP). CuCr LDH and its nanocomposites were successfully fabricated and characterized. Scanning electron microscopy (SEM) along with high-resolution transmission electron microscope (HRTEM) both evidenced the formation of randomly oriented nanosheet structures of CuCr LDH coupled with thin and folded sheets of GO and rGO. The impact of diverse processes on the degradation efficiency of DMP in the presence of the so-prepared catalysts was compared. Benefiting from the low bandgap and high specific surface area, the as-obtained CuCr LDH/rGO represented outstanding catalytic activity (100 %) toward 15 mg L-1 of DMP within 30 min when subjected to light and ultrasonic irradiations simultaneously. Radical quenching experiments and visual spectrophotometry using an O-phenylenediamine revealed the crucial role of hydroxyl radicals compared to holes and superoxide radicals. Overall, outcomes disclosed that CuCr LDH/rGO is a stable and proper sonophotocatalyst for environmental remediation.

A techno-economical assessment of treatment by coagulation-flocculation with aluminum and iron-bases coagulants of landfill leachate membrane concentrates.

Landfill leachate treatment involved with the membrane bioreactor (MBR) combined with membrane treatment via nanofiltration (NF) and/or reverse osmosis (RO) is widely used in Turkey. This treatment produces landfill leachate membrane concentrates (LLMCs) with an undesirably high concentration of contaminants. In the study, two different nanofiltration concentrates of leachate were coagulated. Coagulant dosages from 0.10 to 5.0 g of Me3+/L (Me3+: Al3+ or Fe3+), and the pH values ranged from 4.0 to 8.0 and 3.0-9.0 for Al-based and Fe-based coagulants, respectively. The most efficient pH values were 5.0 and 4.0 for Al3+ and Fe3+, respectively. These pH values are lower than those known to be effective in coagulants. The reason for this is the presence of humic substances in the wastewater. The cost of Fe2(SO4)3.xH2O was the lowest than other coagulants at the end of the cost analyses obtained from Istanbul region landfill leachate NF concentrate (NFCL-1) and Kocaeli region landfill leachate NF concentrate (NFCL-2). Under optimum conditions, the costs for NFCL-1 and NFCL-2 were calculated as 0.55 and 0.46 $/removed kg COD, respectively.

Synthesis of visible light responsive ZnCoFe layered double hydroxide towards enhanced photocatalytic activity in water treatment.

In this study, a ternary layered double hydroxide containing Zn, Co, and Fe transition metals (ZnCoFe LDH) was developed using a co-precipitation procedure. The as-synthesized photocatalyst was evaluated for its performance in the degradation of methylene blue (MB) under visible light irradiation. The effects of various process conditions including photocatalyst dosage, pollutant concentration, pH, lamp distance, and lamp power were investigated. The ZnCoFe LDH achieved approximately 74% photodegradation efficiency owing to the narrow bandgap of 2.14 eV. The Langmuir-Hinselwood rate constants were calculated as 1.17 min-1 and 3.55 min-1 for photolysis by LED lamp alone and for photocatalysis by LED/ZnCoFe LDH, respectively. The photocatalytic ability of the LDH was attributed to the generation of radical species like •OH and O2•-. The photocatalytic degradation intermediates of MB were determined by GC-MS analysis. The catalyst retained its performance throughout seven reuse cycles with only a 4.17% reduction in removal efficiency. The energy per order EEO of the ZnCoFe/LED process in 180 min treatment time was determined as 5.41 kWh.m-3. order-1. This study shows that ZnCoFe LDH has sufficient activity and photostability for long-term application in photocatalytic water treatment.

Removal of arsenic in groundwater from western Anatolia, Turkey using an electrocoagulation reactor with different types of iron anodes.

Electrocoagulation (EC) is a significantly efficient method for As removal from waters and received considerable attention recently. In this study, the natural groundwater (GW) samples containing As concentrations of GW-1: 538.8 µg L-1, GW-2: 1132.1 µg L-1, and GW-3: 52, 000 µg L-1 were obtained from different provinces and treated by EC process using different iron anodes (plate, ball, and scrap). To achieve drinking water As standard (10 µg L-1), the operational time, applied current, and As removal optimization for all anode types were studied. At applied current of 0.025 A, the As removal efficiency, EC time, and operating cost were >99.9%, 180 min and 0.406 $ m-3 for ball anodes, >99.9%, 100 min and 0.0813 $ m-3 for plate anodes, >99.9%, 80 min and 0.0815 $ m-3 for scrap anodes for GW-3, respectively. It was observed that as the As concentration in the GW increased, the EC time and operating cost increased. Overall, it was concluded that Fe scrap anodes are more advantageous than other types of anodes in terms of operating cost in EC reactor for As removal.

Electrochemical oxidation of pretreated landfill leachate nanofiltration concentrate in terms of pollutants removal and formation of by-products.

This study compares the efficiencies of active (Ti/TiO2-RuO2-IrO2 (TIR)) and inactive (Ni/Boron Doped Diamond (BDD)) anodes in terms of pollutant treatment and by-product formation in pretreated (chemical coagulation) landfill leachate nanofiltration membrane concentrate (PLNC). PLNC has high chemical oxygen demand (COD:4900 mg/L), total organic carbon (TOC: 1874 mg/L), total Kjeldahl nitrogen (TKN: 520 mg/L), ammonium nitrogen (NH3-N: 21.35 mg/L), chloride (5700 mg/L) and sulfate (9000 mg/L - due to coagulant type). The parameters of COD, TOC, NH3-N, TKN, free and combined chlorine species, halogenated organic compounds (HOCs), adsorbable organic halogens (AOX), and nitrate at different current density (J: 111-555 A/m2) and initial pH (pHi:3.5-7) were compared for both anodes. The removal efficiencies at the optimum conditions (pHi 5.5, 333 A/m2 and 8 h) were obtained as 86.4% COD, 77.4% TOC, 93.4% TKN, 94.4% NH3-N with BDD and 34.3% COD, 27.3% TOC, 93.7% TKN, 97.4% NH3-N with TIR. According to gas chromatography-mass spectrometry (GC-MS) results obtained under optimum conditions, haloalkane/alkene, halonitroalkane, halonitrile, haloketone, haloalcohols, haloacids, haloaldehydes, haloamines/amides on both electrodes were detected as species of HOCs. In addition, the highest nitrate concentration was observed at the TIR anode, while the highest AOX concentration was observed at the BDD anode.

Nanoarchitecture of graphene nanosheets decorated with NiCr layered double hydroxide for sonophotocatalytic degradation of refractory antibiotics.

Highly efficient and durable catalysts for wastewater treatment are urgently required to tackle critical environmental issues. In this regard, NiCr LDH (NC), NiCr LDH-GO (NC-GO), and NiCr LDH-rGO (NC-rGO) nanocomposites were synthesized. The results of XRD, EDX, and FTIR analyses not only explored the crystallographic and chemical structures of catalysts but also confirmed the successful synthesis. Further morphological, physical, chemical, and optical characteristics of the catalysts were evaluated more by SEM, HRTEM, BET, DRS, and XPS techniques. The as-synthesized catalysts were used for the efficient mineralization of rifadin under 50 W LED visible light irradiation and the ultrasonic power of 150 W. Amongst, 0.75 g L-1 of NC-rGO demonstrated high sonophotocatalytic efficiency (88%) in natural pH (pH = 8) of 15 mg L-1 of rifadin. The introduced system is also powerful for the decontamination of pharmaceutical-containing wastewater as well as other refractory antibiotics. Moreover, the radical trapping experiments demonstrated that the main reactive species involved in the degradation of rifadin are •OH, h+, and O2•-. The possible intermediates were thoroughly investigated using GCMS analysis. Also, NC-rGO demonstrated superior antibacterial activity in comparison with NC, NC-GO samples.

High-performance carbon black electrode for oxygen reduction reaction and oxidation of atrazine by electro-Fenton process.

The aim of this study is to produce an electrode that can be used in H2O2 production and Electro-Fenton (EF) process by an effective, cheap, and easy method. For this reason, a superhydrophobic electrode with a higher PTFE ratio and high thickness was produced with a simple press. The produced electrode was used in the production of H2O2 and mineralization of Atrazine. First, the effect of pH, cathode voltage, and operation time on H2O2 production was evaluated. The maximum H2O2 concentration (409 mg/L), the highest current efficiency (99.80%), and the lowest electrical energy consumption (3.16 kWh/kg) were obtained at 0.8 V, 7.0 of pH, and 120 min, and the stability of the electrode was evaluated up to 720 min. Then, the effects of the operational conditions (pH, cathode voltage, operating time, and catalyst concentration) in electro-Fenton were evaluated. The fastest degradation of Atrazine (>99%) was obtained at 2.0 V, 3.0 of pH, and 0.3 mM of Fe2+ in 15 min. In the final part of the study, the degradation intermediates were identified, and the characterization of the electrode was evaluated by SEM, XRD, FT-IR, tensiometer, potentiostat, and elemental analyzer.

Graphene-based ZnCr layered double hydroxide nanocomposites as bactericidal agents with high sonophotocatalytic performances for degradation of rifampicin.

Herein, ZnCr layered double hydroxide (ZnCr LDH), and its nanocomposites with GO and rGO were synthesized using the co-precipitation method. The samples were characterized using XRD, FT-IR, SEM, TEM, BET, and XPS techniques. The sonophotocatalytic activity of the ZnCr LDH, ZnCr LDH/GO, and ZnCr LDH/rGO was investigated via the degradation of rifampicin (RIF) in the ultrasonic bath under visible light irradiation. The synergy index of more than 1 determined for ZnCr LDH/rGO indicated the positive interaction of sonocatalysis and photocatalysis resulted by hybridizing the LDH nanosheets with rGO. The maximum sonophotocatalytic degradation efficiency of 87.3% was achieved in the presence of ZnCr LDH/rGO nanocomposite with the concentration of 1.5 g L-1 for degradation of RIF with an initial concentration of 15 mg L-1 within 60 min sonication under visible light irradiation. The addition of different scavengers indicated that hydroxyl radicals, superoxide anion radicals, and the generated holes played a dominant role in the degradation of the pollutant molecules. A possible degradation mechanism was suggested based on the intermediates. The antibacterial tests confirmed the higher antibacterial activity of ZnCr LDH/GO compared with ZnCr LDH and ZnCr LDH/rGO against Gram-positive Staphylococcus aureus.

Zinc-chromium layered double hydroxides anchored on carbon nanotube and biochar for ultrasound-assisted photocatalysis of rifampicin.

In this study, ZnCr layered double hydroxide (LDH), ZnCr LDH/carbon nanotube (CNT), and ZnCr LDH/Biochar (BC) were synthesized and characterized by various analyses. The successful synthesis and the great crystallinity of the samples were consented by XRD analysis. SEM and TEM were applied to study the morphology of the synthesized samples. The simultaneous presence of C, Zn, and Cr elements was well confirmed by EDX and dot mapping analyses demonstrating the successful preparation of nanocomposites. According to the BET analysis, ZnCr LDH nanocomposites with BC and CNT had more specific surface area compared to ZnCr LDH alone. The catalytic performances of the samples were determined for the degradation of rifampicin (RF). The degradation efficiency of the sonophotocatalytic process in the presence of 0.6 g L-1 of ZnCr LDH/BC toward 15 mg L-1 of RF under 150 W ultrasound and visible light irradiation was found to be about 100% within 40 min. The influence of the reactive species on the sonophotocatalytic process was assessed via the addition of different scavengers (para-benzoquinone (p-BQ), formic acid (FA), isopropyl alcohol (IPA)), and enhancers (hydrogen peroxide and potassium persulfate). The GC-MS analysis was carried out and eleven by-products during the RF decomposition were detected.

How does arsenic speciation (arsenite and arsenate) in groundwater affect the performance of an aerated electrocoagulation reactor and human health risk?

Arsenic (As) occurrence in water resources has become one of the most critical environmental problems worldwide. The detrimental health impacts on humans have been reported due to the consumption of As-contaminated groundwater resources. Consumption of As-containing water over the long term can cause arsenicosis and chronic effects on human health due to its toxicity. Several treatment processes are available for As removals such as coagulation, ion exchange, adsorption, and membrane technologies but they have various major drawbacks. In the present work, therefore, an aerated electrocoagulation (EC) system with aluminum anodes was operated for simultaneous arsenate (As(V)) and arsenite (As(III)) removal to overcome the disadvantages of other processes such as, sludge formation, difficulties in operation, high operating costs, high energy consumption, and the requirement of pre-treatment process and to enhance the conventional EC process. The combined effects of the applied current (0.075-0.3 A), aeration rate (0-6 L/min), pH (6.5-8.5), and As speciation (As(V)-As(III)) were studied on As removal efficiency. The findings revealed that As removal mostly depended on the airflow rate and the applied current in the EC system. The highest As removal efficiency (99.1%) was obtained at an airflow rate of 6 L/min, a pH of 6.5, an initial As (V) concentration of 200 µg/L, and a current of 0.3 A, with an energy consumption of 2.85 kWh/m3 and an operating cost of 0.66 $/m3. The human health risk assessment of treated water was also examined to understand the performance of the EC system. At most of the experimental runs, the chronic toxic risk (CTR) and carcinogenic risk (CR) of As were within the permissible limits except for an airflow rate of 0-2 L/min, an initial pH of 8.5, and a current of 0.075-0.15 A for high initial As (III) concentrations. Overall, the As removal performance and groundwater risk assessment show that the EC process is a promising option for industrial applications.

A study of inline chemical coagulation/precipitation-ceramic microfiltration and nanofiltration for reverse osmosis concentrate minimization and reuse in the textile industry.

Reverse osmosis concentrate (ROC) is one of the major drawbacks in membrane treatment technologies specifically due to the scale-forming ions. It is important to remove these ions from ROC to enhance total water recovery and reuse in the textile industry that is the largest water-consumer and polluter industry. In this work, coagulation/high pH precipitation (CP) integrated with ceramic microfiltration (CMF) was studied as a pre-treatment method followed by nanofiltration (NF) to increase the efficiency of water recovery. To prevent organic fouling, ferric chloride (FeCl3) was applied at a concentration of 3 mM, and ceramic membranes were used for the removal of non-precipitating crystals and/or suspended solids (at high pH) before the NF processes. The CP-CMF method successfully removed calcium (Ca2+), magnesium (Mg2+), silica (SiO2), and TOC up to 97, 83, 92, and 87% respectively, which resulted in higher performance of the NF process. Moreover, this method provided higher flux at lower pressure that ultimately increased overall water recovery of the NF process to achieve near-zero liquid discharge (n-ZLD). A cost-benefit estimation showed that a high-quality effluent (COD<5 mg/L; conductivity 700<µS/cm; negligible residual color) can be generated and recycled in the textile industry at an economical cost (approximately 0.97 USD/m3). Therefore, ROC minimization and water recovery can help to achieve n-ZLD using the CP-CMF/NF method.

Toxicity of Zn-Fe Layered Double Hydroxide to Different Organisms in the Aquatic Environment.

The application of layered double hydroxide (LDH) nanomaterials as catalysts has attracted great interest due to their unique structural features. It also triggered the need to study their fate and behavior in the aquatic environment. In the present study, Zn-Fe nanolayered double hydroxides (Zn-Fe LDHs) were synthesized using a co-precipitation method and characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and nitrogen adsorption-desorption analyses. The toxicity of the home-made Zn-Fe LDHs catalyst was examined by employing a variety of aquatic organisms from different trophic levels, namely the marine photobacterium Vibrio fischeri, the freshwater microalga Pseudokirchneriella subcapitata, the freshwater crustacean Daphnia magna, and the duckweed Spirodela polyrhiza. From the experimental results, it was evident that the acute toxicity of the catalyst depended on the exposure time and type of selected test organism. Zn-Fe LDHs toxicity was also affected by its physical state in suspension, chemical composition, as well as interaction with the bioassay test medium.

Degradation of thiocyanate by electrochemical oxidation process in coke oven wastewater: Role of operative parameters and mechanistic study.

This study presents the removal of thiocyanate (SCN-) from coke oven wastewater by the electrooxidation (EO) process. Initially, the performances boron-doped diamond (BDD) and different DSA (Dimensionally stable anode) electrodes including Ti/IrO2, Ti/IrO2-RuO2, and Ti/IrO2-RuO2-TiO2 in SCN- removal were compared. BDD anode outperformed the Ti-based mixed metal oxide (MMO) anodes achieving 96.51% SCN- removal efficiency. The most favorable conditions for the removal of SCN- using BDD anode were determined as follows: pH = 9, current density = 43.10 A m-2, and the electrolyte concentration (Na2SO4) = 2.5 g L-1. The strong role of ⦁OH in the removal of SCN- was confirmed by the addition of radical quenching agents. The evolution of the intermediates as a result of the EO of SCN- was determined. Under the determined conditions, the EO process could remove 84.13% of SCN- and 94.67% of phenol from a real coke oven wastewater, which was comparable to that of the simulated solution. The electrical energy consumption cost of the process to remove 1 kg of SCN- was calculated as 0.208 US $. Overall, the study showed the EO using BDD anode is a cost-effective method for the removal of SCN- from a coke oven wastewater.

Influence of arsenic and boron on the water quality index in mining stressed catchments of Emet and Orhaneli streams (Turkey).

Emet and Orhaneli stream basins are characterized by intense mining of colemanite, the main borate mineral in the area. Unlike other global borate deposits, the colemanite of this region contains arsenic minerals (realgar and orpiment). Undoubtedly, improper management of mine wastes causes pollution of water resources, affecting human life and biota. In the present study, spatial and temporal variation in water quality of Emet and Orhaneli streams was assessed. The water quality index (WQI) model was used to rate the overall status of the water, and geographical information systems (GIS) was used to aid the visualization of results. No significant differences in WQIs for the three-monitoring periods (March, July and October 2017) were noted. The WQI in the region is highly influenced by arsenic (As) and boron (B), with a strong positive correlation (p < 0.05, r2 = 0.971). The As and B concentrations in Emet stream were 1.88-1907 µg/L and 0.01-1900 mg/L, respectively. Whereas for Orhaneli stream, respective As and B levels ranged from 5.17 to 116 µg/L and 0.01 to 5.45 mg/L. Globally, the As level in Emet stream basin is comparable to some of the words major contaminated regions such as Rapti River Basin (India) and Xieshui River (China). However, the uniqueness of this basin is seen in B and As trends, and input routes like active geothermal waters and weathering of the realgar (AsS) and orpiment (As2S3) from colemanite nodules. This paper demonstrates the influence of pollutants associated with basin geochemistry and exploration of mineral resources on WQI.

Synthesis of g-C3N4@CuMOFs nanocomposite with superior peroxidase mimetic activity for the fluorometric measurement of glucose.

Herein, a novel metal-organic framework (MOF) based nanocomposite with efficient catalytic behavior is reported including flake-like copper (II) MOF (CuMOF) and graphitic C3N4 nanosheets (g-C3N4). The g-C3N4@MOF nanocomposite was simply prepared by solvothermal synthesis of CuMOF in the presence of g-C3N4. The characterization analyses using scanning electron microscopy (SEM), X-ray diffractometry (XRD) and some other techniques demonstrated a nano-porous flake-like structure for the synthesized CuMOF, which enveloped the g-C3N4 nanosheets. Furthermore, the investigation of catalytic behavior of synthesized nanomaterial was implemented on H2O2 based reactions. The fluorometric and colorimetric experimentations illustrated that the accompanying of g-C3N4 with CuMOF had a remarkable positive effect on the catalytic behavior of obtained g-C3N4@MOF. This effect was described based on the improved affinity of nanocomposite to adsorb H2O2 and also synergistic action of its components on the dissociation of H2O2 to hydroxyl radicals. Finally, the analytical application of high catalytic activity of new g-C3N4@MOF was designed for the rapid and simple measurement of glucose in blood. After the enzymatic oxidation of glucose, the fluorometric method was applied for the analysis of produced H2O2 using terephthalic acid as peroxidase substrate. The system led to the ultrasensitive glucose determination in the concentration range of 0.1-22 µM, with a detection limit (3S/m) of 59 nM.

Heavy metal pollution and spatial distribution in surface sediments of Mustafakemalpasa stream located in the world's largest borate basin (Turkey).

Mining activities in addition to the geology of Mustafakemalpasa catchment have for long been linked to its deteriorating water and sediment quality. This study assessed contamination levels of heavy metals and other major elements (Pb, As, B, Cd, Zn, Cr, Mo, Co, Ni, Cu, and Ag) in surface sediments of the area, and identified possible pollution sources. Sediment quality indicators, such as contamination factor (CF), enrichment factor (EF), geo-accumulation index (Igeo) and sediment quality guidelines were used, in addition to multivariate statistical technics; Pearson Correlation Matrix (PCM), Principal Component Analysis (PCA) and Hierarchical Cluster Analysis (HCA). The highest contamination (annual average > 110 mg kg-1) was revealed by B, Cr, Ni, Zn and As. Moreover, As, Cd and Ni levels exceeded their respective probable effect concentrations (PEC), posing a potential negative impact to biota. The highest Igeo values were recorded for Cr, B, Ni, As and Zn, and occurred near urban settlements and mining sites, particularly of coal and chromium. The present study also suggests use of site rank index (SRI) as an alternative to pollution load index (PLI), since the former is derived from the data of interest and eliminates arbitrary classifications. The sources of heavy metals in the sediments were attributed to fly ashes of coal-powered plants, urban waste leachate and weathering of sulfide ore minerals for Pb, Zn and Cu; urban-industrial wastes and mining wastes for Ni. Although Cr, As, Cd and B were ascribed to natural occurrence, their presences in river sediment is accelerated by mining.

Acid production potentials of massive sulfide minerals and lead-zinc mine tailings: a medium-term study.

Weathering of sulfide minerals is a principal source of acid generation. To determine acid-forming potentials of sulfide-bearing materials, two basic approaches named static and kinetic tests are available. Static tests are short-term, and easily undertaken within a few days and in a laboratory. In contrast, kinetic tests are long-term procedures and mostly carried out on site. In this study, experiments were conducted over a medium-term period of 2 months, not as short as static tests and also not as long as kinetic tests. As a result, pH and electrical conductivity oscillations as a function of time, acid-forming potentials and elemental contents of synthetically prepared rainwater leachates of massive sulfides and sulfide-bearing lead-zinc tailings from abandoned and currently used deposition areas have been determined. Although the lowest final pH of 2.70 was obtained in massive pyrite leachate, massive chalcopyrite leachate showed the highest titrable acidity of 1.764 g H2SO4/L. On the other hand, a composite of currently deposited mine tailings showed no acidic characteristic with a final pH of 7.77. The composite abandoned mine tailing leachate had a final pH of 6.70, close to the final pH of massive galena and sphalerite leachates, and produced a slight titrable acidity of 0.130 g H2SO4/L.