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In the present study, continuous-flow column experiments (using glass column, Tygon tubing, and peristaltic pump Manostat Carter) were conducted to investigate the performance of permeable sorption barriers for the removal of cadmium and zinc from synthetic groundwater. Zeolite, ionexchange resin and granular activated carbon as reactive materials were used. The effectiveness and stability of reactive materials were studied by monitoring of changes of metal ions concentration and selected background anions and cations concentration in groundwater during its flow through columns. Results showed that ion exchange resin was the most effective material of permeable reactive barrier (PRB). Performance of resin barrier remained effective (>99.5% metal ions removal) for the time corresponding to on average of about 10,000 min. The high efficiency of ion-exchange resin in PRB for removal of heavy metals from groundwater was coupled with its reactivity and long barrier lifetime. The breakthroughs in the column tests on activated carbon and zeolite using synthetic groundwater occurred much earlier as compared to resin. Therefore, the system using resin requires smaller amount to treat a given volume of groundwater as compared to other materials. Moreover, the presence of other ions did not impact on activity and permeability of barrier filled with resin. [ABSTRACT FROM AUTHOR]

This paper aims to assess the performance of a distributed hydrological model for simulating the transport of various heavy metals in rivers, to enhance and support environmental monitoring strategies for rivers in developing countries. In this context, we evaluated the performance of the Geophysical flow Circulation (GeoCIRC) model based on Object-Oriented Design (OOD) for the simulation of contamination from multiple heavy metals (Pb, Hg, Cr, and Zn) in Harrach River in Algeria. The results of the case study were in good agreement with the observations. Methodology for the assessment of data quality control and the improvement of monitoring procedures was proposed by using the hydrological model to simulate different scenarios. The GeoCIRC-model-based OOD allowed the prediction of the concentrations of heavy metals with minimal input data. Also, various heavy metals could be numerically treated simultaneously because the OOD increases the model's flexibility to allow the handling of many transportable materials. Therefore, the GeoCIRC model is a powerful tool for the monitoring of environmental contamination in rivers by various heavy metals. [ABSTRACT FROM AUTHOR]

A catalytic ozonation--microbial fuel cell and Acidithiobacillus ferrooxidans leaching process was used in treating flotation wastewater to remove chemical oxygen demand (COD) and heavy metals in this study. The results indicated that when adding 1 g/L of manganese/modified activated carbon catalyst and 1.5 g/min ozone flow, the COD could be degraded from 2,043.67 mg/L to 711.4 mg/L. After that, the COD could continue decreasing down to 72.56 mg/L through an air-cathode single chamber microbial fuel cell (SCMFCs), coated with 0.4 mg/cm² platinum catalyst, after 15 days. Meanwhile, the maximum voltages and the ultimate power density of the SCMFCs reached 378.96 mV and 7,608.35 mW/m², respectively. For filter residue, when 1.2 g/L Fe3+, 10% (m/v) filter residue, and 10% Acidithiobacillus ferrooxidans were added, the copper leaching rate could reach 92.69% after 7 days if the pH values were adjusted to 1.9. Furthermore, the other heavy metals were also decreased to a level lower than the pollution control standard (Chinese standard GB3838-2002). The leaching parameters in terms of pH, redox potential, and cyclic voltammetry showed that the addition of an appropriate concentration of Fe3+ to the leaching systems was beneficial to copper dissolution. [ABSTRACT FROM AUTHOR]

Untreated combined sewer overflows (CSOs) cause serious water pollution problems. In this study, the effects of CSO-induced heavy metals and the remediation practice of installation of a long-term water diversion (LTWD) on the microbial environment in river sediments were analyzed in an inland river. The Zn, Cd, Cr, and Cu contents in sediments and water were analyzed. DNA extraction and polymerase chain reaction analysis were conducted based on the Illumina MiSeq platform. The results showed that CSOs have a significant adverse impact on the diversity of microbial populations in river sediments. The LTWD is helpful in improving the richness of microorganisms and the proportion of Gram -ves, but it is challenging to reduce the accumulation of heavy metals in the sediment. The correlation analysis shows a strong relationship between some metabolic pathways and Zn and Cd accumulation in river sediments. Some detoxification compound metabolisms are also promoted at these sites. Thus, chronic exposure to environmental heavy metals from CSOs decreases the river microbial community, and further affects the ecological environment of the river. Therefore, without eliminating CSOs or reducing overflow frequency, it is difficult to alleviate the accumulation of heavy metals in river sediments and improve river ecology via water diversion alone. [ABSTRACT FROM AUTHOR]

In this paper, the removal performance and mechanism of xanthated chitosan (XCTS) towards heavy metal ions are investigated. XCTS possesses both strong chelating abilities and excellent flocculation properties, which can effectively remove several kinds of heavy metal ions, such as Cr3+, Cu2+, Mn2+, Ni2+, Pb2+ and Zn2+. It has a good potential for practical application. In a flocculation test of a mixed component solution, the removal rates of Cr3+, Cu2+ and Cd2+ reach 100%, 100% and 99.1%, respectively. The removal rates are significantly greater than that of a single component solution. It indicates that there is a synergistic effect between different metal ions. Moreover, the selectivity of XCTS for Cr3+ and Cu2+ is obviously superior to that for Cd2+; XCTS is easier to combine with the heavy metal ions belonging to hard acids. [ABSTRACT FROM AUTHOR]

This research analyzes the use of natural shrimp shell and commercial chitin for biosorption of metal ions in surface runoff. Investigation of the use of these biosorbent materials in drainage systems becomes a management measure for two extremely important issues in Brazil, fish waste management and the surface runoff quality. Methodological procedures involved treatments with different amounts of unprocessed shrimp shell and commercial chitin (5 g and 10 g) for 200 mL of a compensatory drainage mechanism (infiltration swale). The contact time of biosorbent and runoff was 24 h and removal of metal ions Fe, Mn, Zn, Cu, Ni, Pb, and Cr was studied. Tests with unprocessed shrimp shell showed high concentrations of metallic ions (Pb, Ni, and Cu) causing contamination of the environment. However, the two biosorbents presented good removal of specific metallic ions (Fe, Mn, Zn, and Cr). These results indicate the need for a biosorbent pre-treatment prior to full-scale use. We indicate the need for a more detailed investigation of water quality in the environment used for shrimp farming. Tests with commercial chitin presented satisfactory results for two concentrations tested. Tests with 10 g of commercial chitin allowed removal of all tested metal ions (Fe, Mn, Zn, Cu, Ni, Pb, Cr) with removal percentage between 6.7% and 84.4%. This efficiency may be related to the chitin's composition (shrimp, crustaceans, and crab) and to the chemical process applied to the product prior to commercialization. [ABSTRACT FROM AUTHOR]

Given the adverse health effects of antimony (Sb), there is an increased focus on developing methods to remove this toxic metal from contaminated water bodies. To effectively remove Sb(V), a new nanostructured Fe--Cu--Al trimetal oxide was fabricated using co-precipitation method at ambient temperature. The Fe--Cu--Al trimetal oxide was very effective at removing Sb(V) from water; it had a maximal adsorption capacity of 169.1 mg/g at pH 7.0, a capacity that was competitive with most other reported adsorbents. The obtained amorphous oxide had a high pH point of zero charge (pHpzc = 8.8) and good adsorption Sb(V) efficiency over a wide pH range (4.0-8.0). Sb(V) uptake was achieved mainly through an ion-exchange reaction between Sb(V) ions and hydroxyl groups on the surface of the oxide. Given its good removal performance, high selectivity, and simple synthesis, this novel Fe--Cu--Al trimetal oxide offers a promising alternate for removing antimony contamination from aquatic environments. [ABSTRACT FROM AUTHOR]

A combined high-rate algal pond and submerged macrophyte pond (APMP) reactor was introduced as a novel biotechnique for efficient heavy metals (HMs) removal from wastewater. The role of water temperature, light regime, and N:P mass ratio on algae growth and HMs removal as well as effects of macrophyte species and densities on algae extermination were investigated through batch experiments. Results showed that water temperature significantly affected algae proliferation and HMs removal. Effects of light regime and N:P only showed obvious influences on HMs removal performance at high temperature. HMs removal efficiency reached 75.8% (Cr), 63.6% (Pb), and 61.1% (Zn) at 5-day hydraulic retention time (HRT) in APMP. Positive correlation existed closely between HMs removal and algal growth with long HRT. Algae were strongly inhibited by Ceratophyllum demersum and Vallisneria natans at plant density of 20-30 rhizomes m-2 with effluent algae concentration about 1,000 cells mL-1 at 7-day HRT. Results suggested that the APMP reactor was efficient for HMs removal from wastewater, indicating a possible effective metals removal technique by using APMP. [ABSTRACT FROM AUTHOR]

The presence of heavy metals in the environment has increased, and cadmium (Cd) and zinc (Zn) are considered to be among the most dangerous. An upflow Al-electrocoagulation reactor was used to remove Cd2+ and Zn2+ ions from aqueous media. The system consisted of perforated aluminum circular electrodes for fluid distribution with elimination of external agitation. The effect of different parameters, i.e. current intensity, electrolysis time, concentration of Cd2+ and Zn2+ ions and electrolytic support dose were optimized by response surface methodology. The results indicated that increasing the current intensity and the electrolysis time had a positive effect on the elimination efficiency of the pollutant ions. Likewise, increasing the dose of electrolytic support and decreasing the concentration of the pollutants improved the efficiency of the system. The optimal results were: current intensity of 0.4 A, electrolysis time of 40 min, ion concentration of 44.6 mg·L-1 and electrolytic support dose of 0.56 mg·L-1, with the maximum elimination percentages of 96±3.8% and 96±2.7% for Cd2+ and Zn2+, respectively. This study showed that the electrocoagulation process in an upflow electrocoagulation reactor could be successfully applied to remove pollutants from water. [ABSTRACT FROM AUTHOR]

Heavy metal contamination from electroplating wastewater is a serious risk to terrestrial life and public health. The complexed metal cannot be effectively removed by traditional precipitation without decomplexing. In this work, four ozone-based advanced oxidation processes, O3, O3/H2O2, O3/UV and O3/H2O2/UV to decomplex electroplating wastewater were investigated and their performance compared. Ethylenediaminetetraacetic acid (EDTA) and citric acid are the most common components of electroplating wastewater. They were used as representatives to study the decomplexation and mineralization of complexes in the ozone-based advanced oxidation processes. Among all, the highest degradation and mineralization efficiency of EDTA occurred in O3/UV and was 65% and 53% in 60 min, respectively. For citric acid, the highest degradation (77%) and mineralization (56%) efficiency was observed in the O3/H2O2/UV process. This indicates that selection of the advanced oxidation process is determined by the target contaminant. [ABSTRACT FROM AUTHOR]

Excessive industrialization and anthropogenic activities have resulted in widespread prevalence of heavy metals including hexavalent chromium in the environment. In addition to toxic properties, Cr(VI) possesses high stability and mobility, which in total makes it included in the list of priority heavy metals; thus it needs to be managed urgently. Among different methods available for remediation of Cr(VI), bioremediation is considered as one of the sustainable methods which could effectively be utilized for controlling Cr(VI) pollution. In this aspect, the treatment of Cr(VI)-containing wastewater originating from industries is noteworthy. The present review thus is an attempt to present a systematic overview dealing with studies on remediation of hexavalent chromium by using microorganisms and their application in treatment of Cr(VI)--containing industrial wastewaters. Various factors affecting the Cr(VI) removal and methods to enhance the bio-treatment are highlighted, which might act as a basis for researchers developing Cr(VI) bioremediation techniques. [ABSTRACT FROM AUTHOR]

Bioremediation is preferred in heavy metal remediation, and the high-performance microbe is of prime importance. In the present research, three Pb-resistant microbes were isolated and growth characteristics and adsorption capacities were evaluated. The results showed that R. oryzae SD-1, T. asperellum SD-5, and M. irregularis SD-8 can grow well under 100 mg L-1 Pb2+ ions stress. There is a higher minimum inhibitory concentration (MIC) of Pb but lower MICs of Cd and Zn in T. asperellum SD-5. However, there were similar MICs of Cu among the three microbes. R. oryzaeSD-1 exhibited a higher adsorption capacity and removal rate relative to the other two microbes under various Pb2+ ion levels. The Langmuir equation was fitted for the adsorption capacity of T. asperellum SD-5 and M. irregularis SD-8, and their maximum adsorption capacities were approximately 456.62 mg g-1 and 93.62 mg g-1. Moreover, the Elovich equation and the double constant equation can describe the adsorption process of Pb2+ ions in Pb-resistant microbes well. The strongest adsorption capacity under lower Pb2+ ion level was observed in M. irregularis SD-8, while the strongest adsorption capacities under higher Pb2+ ion levelswere seen in R. oryzae SD-1 and T. asperellum SD-5. Therefore, three novel Pb-resistant microbes may be used as efficient, easily cultivated materials for Pb-contaminated soil remediation. [ABSTRACT FROM AUTHOR]

Heavy metals released from urban areas have toxic effects on aquatic organisms. Heavy metals in aquatic environments exist in various forms and methods designed to assess their effects need to consider their bioavailability. This study aimed to explore biomarkers in an estuarine amphipod, Grandidierella japonica, for exposure to heavy metals using metabolomics. We exposed G. japonica to different heavy metals and analyzed their metabolomes using high-resolution mass spectrometry. Partial least squares discriminant analysis (PLS-DA) was used to extract biomarkers of exposure for each heavy metal. As a result, three models were built to predict discrimination based on metabolomic profiles, and 70, 106, and 168 metabolites were extracted as biomarkers for exposure to Cu, Zn, and Cd, respectively. Our results suggest that PLS-DA was effective in extracting biomarkers, and this study demonstrated the usefulness of metabolomics as biomarkers. [ABSTRACT FROM AUTHOR]

Magnetically recoverable chitosan based spinel cobalt and nickel ferrite (CS/CoFe2O4 and CS/NiFe2O4, respectively) composites were successfully prepared in one step. A series of batch adsorption experiments indicated that the removal of toxic Cd(II) ions by the as-obtained composites as adsorbents was pH-dependent, rapid, proficient, better fitted to pseudo-second-order kinetics model and Langmuir monolayer adsorption isotherm model. Compared to the naked particles, magnetic bio-polymer composites exhibited promoted adsorption capacity. Competitive adsorption studies in binary solutions illustrated preferable selectivity of adsorbents toward Cd(II) ions in the presence of co-existing cations. More importantly, CS/CoFe2O4 and CS/NiFe2O4 had a satisfactory practical application in the removal of Cd(II) from real groundwater spiked with cadmium. The exhausted adsorbents could be regenerated efficiently by 0.5 M HNO3. The results from this study support that CS/CoFe2O4 and CS/NiFe2O4 prove excellent adsorption behavior for the removal of Cd(II) ions from aqueous media. [ABSTRACT FROM AUTHOR]

In this study, laboratory-scale green (e.g. living) roof platforms were established to assess the potential use of polluted river sediment in their substrate mixture. The mean runoff retention of the green roof platforms, which contained peat and/or river sediment, after 11 artificial rainfall events was >72%, significantly higher than traditional roofs. However, green roof platforms that had been filled with peat soil showed chemical oxygen demand (COD), total nitrogen (TN) and total phosphorus (TP) leaching. Green roofs that had used river sediment showed good leaching control for COD, TN and TP. The cumulative leaching masses from the green roofs contained 30% (COD), 42% (TN) and 47% (TP) as much as the total leaching mass from traditional roofs, and the Cu, Zn, Cd and Pb leaching risk from green roofs when river sediments are used as part of a substrate mixture was relatively low. Despite some nutrient leaching in the initial phase of runoff from the green roofs, river sediment has the potential to be used as a substrate for extensive green roofs. [ABSTRACT FROM AUTHOR]

It is of practical significance to promote the transformation of Fe in acid mine drainage (AMD) into ferric hydroxysulfate minerals with strong ability to remove heavy metals or metalloids. To investigate the types of biogenic ferric hydroxysulfate minerals generated in AMD by Acidithiobacillus ferrooxidans (A. ferrooxidans), different pH and K+ concentrations are tested for the formation of precipitates in media containing 160 mmol/L Fe2+. The Cr(VI) removal efficiencies of ferric hydroxysulfate minerals in AMD with different acidities are also compared. Results indicate that the mineralizing abilities of the initial pH levels (pH 3.0 >pH 2.5 >pH 2.0) and K+ concentrations (53.3 mmol/L>3.2 mmol/L ≈ 0.8 mmol/L) differ, with cumulative Fe precipitation efficiencies of 58.7%, 58.0%, and 44.2% (K+ = 53.3 mmol/L), and 58.7%, 29.9%, and 29.6% (pH 3.0) after 96 h of A. ferrooxidans incubation, respectively. X-ray diffraction indicates that K-jarosites are formed in the treatments n(Fe)/n(K) = 0.1 and 3 at pH 2.0-3.0, while only schwertmannite is generated in a system of pH 3.0 and n(Fe)/n(K) = 200. X-ray photoelectron spectroscopy reveals that HCrO4- may be adsorbed as an inner-sphere complex on schwertmannite when the AMD pH is 3.0. [ABSTRACT FROM AUTHOR]

Struvite (MgNH4PO4·6H2O) crystallisation is a promising approach for phosphorus recovery from swine wastewater. Currently, intensive pig feeding has made heavy metals (HMs) extensive in swine wastewater; therefore, significant amounts of HMs have been detected in struvite recovery products. In this study, the HM residues in the struvite products recovered from stirred and fluidised bed reactors were investigated. The results showed that Zn, Mn, and Cu were the most abundant elements in swine wastewater (1,175.3±178.0, 745.4±51.5, and 209.3±54.4 μg L-1, respectively). The HMs, especially Zn (97.0%) and Cu (96.8%), were mainly distributed in the total suspended solids (TSS) of the swine wastewater. Redundancy analysis revealed that the HMs in the struvite products harvested from the fluidised bed reactor were mainly attributable to the aggregation of dissolved matters, because most TSS were elutriated through fluidisation. In contrast, the HMs in the struvite products harvested from the stirred reactor mainly originated from the TSS, which complexed with the HMs, and co-precipitated and settled with the struvite products. Furthermore, chemical fractionation of the HM species confirmed that the presence of HMs in the struvite products was mainly attributable to metal precipitation and organic aggregation. [ABSTRACT FROM AUTHOR]

Bioleaching has been demonstrated to be an effective technology for the removal of heavy metals and sludge dewaterability. Since bacteria gain nutrients by diffusion of soluble compounds, the insolubility of elemental sulfur may slow the growth of bacteria. Thus, it is very important to find an energy substance quickly become available to Acidithiobacillus thiooxidans. This paper studies the improvement of sludge dewaterability and heavy metal removal with sodium thiosulfate as the source of energy for Acidithiobacillus thiooxidans. Through orthogonal experiments with specific resistance to filtration (SRF) as the target index, four factors (FeSO4 dosage, Na2S2O3 dosage, sludge reflux ratio and sludge moisture content) were identified to be the important influencing parameters. The optimal conditions were: FeSO4 dosage, 8 g/L; Na2S2O3 dosage, 1.5 g/L; sludge reflux ratio, 30%; sludge moisture content, 97%. Results indicated that the SRF of the sludge decreased from 9.89 x 1012 to 1.03 x 1011 m/kg. The removal efficiencies of heavy metals Cu, Zn, Pb and Cr could reach 83%, 78%, 31% and 38% within 3 days, respectively. These results confirm the potential of sodium thiosulfate as an alternative energy substance in bioleaching to improve sludge dewaterability as well as removal of metals. [ABSTRACT FROM AUTHOR]

Although rice husk (RH) is a readily available, natural, heavy metal adsorbent, adsorption capacity in its natural form is insufficient for certain heavy metal ions. In this context, the study is based on enhancement of the adsorption capacity of RH for Cu(II). NaOH modified rice husk (SRH) shows higher extent of removal for Cu(II) ions than that of heated rice husk (HRH) and HNO3 modified rice husk (NRH). The extent of removal of SRH is increased with the concentration of NaOH, and the optimum NaOH concentration is 0.2 mol dm-3, used to modify rice husk for further studies. The surface area of SRH is 215 m²g-1, which is twice as much as that of HRH according to previous studies. The sorption of Cu(II) on SRH obeys the Langmuir adsorption model, leading to the maximum adsorption capacity of 1.19 x 104 mg kg-1. Kinetics studies show that the interaction of Cu(II) with SRH obeys pseudo second order kinetics. The X-ray fluorescence spectroscopy confirms the adsorption of Cu(II) on SRH, while desorption studies confirm that Cu(II) adsorbed on SRH does not leach it back to water under normal conditions. [ABSTRACT FROM AUTHOR]

In this present study, biosorption of Zn(II) from aqueous solution by cyanobacterium Fischerella ambigua was investigated in batch experiments. The effects of pH, bacterial dosage, initial Zn(II) concentration, contact time and temperature were studied. Removal process was influenced significantly by the variation of pH, biosorbent concentration, initial Zn(II) ion concentration, temperature and contact time. Optimum biosorption conditions were found to be initial pH of 5, bacterial dosage of 0.2 g/l and initial Zn(II) ion concentration of 175 mg/l at room temperature and contact time of 90 min. The maximum uptake capacity of Fischerella ambigua for Zn(II) ions was found to be 98.03 mg/g at optimum conditions. The correlation coefficient for the second-order kinetic model was 0.995. The Freundlich isotherm model showed better fit to the equilibrium of the system, compared with the Langmuir model. Fourier transform infrared analysis of bacterial biomass revealed the presence of carboxyl, hydroxyl, sulfite and amino groups, which are likely responsible for the biosorption of Zn(II). The negative values of Gibbs free energy, ΔG°, confirm the spontaneous nature of the biosorption process. Finally, Fischerella ambigua adsorption capacity was compared with other biosorbents. Results showed that Fischerella ambigua was an efficient biosorbent in the removal of Zn(II) ions from an aqueous solution. [ABSTRACT FROM AUTHOR]

We report the optimization with response surface methodology (RSM) for adsorption conditions required for removal of Cd(II) from an aqueous environment with 3-mercaptopropyl trimethoxysilanemodified bentonite (MMB). Central composite design (CCD) in RSM was used to optimize the most significant adsorption variables of initial pH, temperature (°C), initial Cd(II) concentration (Co, mg L-1) and adsorbent dosage (g). With the quadratic model equation obtained from CCD, the optimum values were determined as initial pH 6.40, temperature 20 °C, Co 49.55 mg L-1 and adsorbent dosage 0.17 g. Under optimum conditions, the optimum adsorption amount of Cd(II) was 27.55 mg Cd(II)/g adsorbent and adsorption yield was 94.52%. The obtained results showed that the Langmuir and Dubinin Radushkevich (D-R) adsorption isotherms were more suitable for adsorption equilibrium data. The kinetic studies indicated that the pseudo-second-order kinetic model was fitted to the adsorption kinetic data. Additionally, thermodynamic studies indicated that the adsorption process was spontaneous and exothermic. As a result, MMB can be chosen as an effective adsorbent for treating heavy metals such as Cd(II) in wastewater and removing them from aqueous solutions. Furthermore, it is thought that it will positively contribute to the literature since the adsorbentadsorbate combination (MMB-Cd(II)) is used for the first time. [ABSTRACT FROM AUTHOR]

In many parts of the world, cadmium metal concentration in drinking water is higher than some international guideline values. To reduce its level below the safety limit, a sustainable and environmental friendly approach is crucial. Thereby, present article introduce an efficient, non-pathogenic and a novel fungal biosorbent Pleurotus eryngii for the removal of Cd(II) ions from aqueous system. The efficiency of P. eryngii were improved and optimized by investigating many significant factors such as; pH, biosorbent dose, initial Cd(II) ion concentration, temperature and contact time. Maximum Cd(II) ions removal (99.9%) was achieved at pH 5.0, biosorbent dosage 0.2 g/10 mL, concentration 20 mg L-1, time 10 min and temperature 50 °C. The isotherm and kinetic models revealed bioremediation of Cd(II) ions as monolayer coverage with biosorption capacity of 1.51 mg g-1 following pseudo second order reaction. Moreover, thermodynamic parameters such as ΔG°, ΔH°, and ΔS° showed that the removal of Cd(II) ions is spontaneous and endothermic in nature. Batch elution process revealed that the complete elution of Cd(II) ions from the biomass were achieved using 0.1 N HNO3 solution. The sorption efficiency decreased from 99.99 to 56.89% as the biomass were recycled up to five times. The efficiency of Cd(II) ions removal from real water samples lies between 85 and 90%. Fourier transform infrared (FTIR) spectrometry, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopic (EDS) and atomic force microscopic (AFM) analysis of fungal biomass confirmed that the Cd(II) ions were the most abundant species on the biomass surface after the sorption process. [ABSTRACT FROM AUTHOR]

It is hard to balance high water permeability and good mechanical strength of hydrogel adsorbents. In this study, an enhanced double network hydrogel adsorbent of poly (vinyl alcohol)/poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (PVA/PAMPS) was prepared via simple free-radical polymerization. Hydrophilic PAMPS guaranteed high swellability of the adsorbent, which made the sufficient diffusion of metal ions towards adsorbent inside. Meanwhile, the cross-linkage between PVA and PAMPS chains ensured good mechanical strength of the adsorbent. Significantly, the introduction of multifunctional groups (-NHR, -SO3H and -OH) endowed the adsorbent with both chelation and ion exchange function for enhancing heavy metal adsorption. The maximum adsorption capacities of Pb2+ and Cd2+ reached 340 and 155.1 mg/g, respectively. The adsorbent could efficiently remove heavy metals in melting effluent, especially Pb2+ and Cd2+. The removal efficiencies reached 88.1% for Pb2+, 91.4% for Cd2+, 70.4% for Zn2+, 77.4% for Cu2+, 42.5% for Mn2+, 45.1% for Ni2+ and 95.4% for Fe2+ using 2 g/L adsorbent in 2 h. Moreover, the adsorbent showed a good reusability, and the removal efficiencies maintained 94% for Pb2+ and 93% for Cd2+ in the fifth cycle (m/V = 1 g dry gel/L). This work developed a highly practical hydrogel adsorbent for heavy metal removal from wastewater. [ABSTRACT FROM AUTHOR]

A mix of microalgae and bacteria was cultivated on pre-sedimented municipal wastewater in a continuous operated microalgae-activated sludge process. The excess material from the process was co-digested with primary sludge in mesophilic and thermophilic conditions in semi-continuous mode (5 L digesters). Two reference digesters (5 L digesters) fed with waste-activated sludge (WAS) and primary sludge were operated in parallel. The methane yield was slightly reduced (≈10%) when the microalgal-bacterial substrate was used in place of the WAS in thermophilic conditions, but remained approximately similar in mesophilic conditions. The uptake of heavy metals was higher with the microalgal-bacterial substrate in comparison to the WAS, which resulted in higher levels of heavy metals in the digestates. The addition of microalgal-bacterial substrate enhanced the dewaterability in thermophilic conditions. Finally, excess heat can be recovered in both mesophilic and thermophilic conditions. [ABSTRACT FROM AUTHOR]

Natural zeolite has been recognized as a useful adsorbent for wastewater treatment for removing cations. Natural zeolite is a kind of porous material with large specific surface area but limited adsorption capacity. In recent years, emphasis has been given to prepare the surface modified zeolite using various procedures to enhance the potential of zeolite for pollutants. Modification treatment for zeolite can greatly change surface chemistry and pore structure. The article describes various modification methods of zeolite, and introduces the removal mechanisms of common pollutants such as ammonium, phosphorus and heavy metals. In addition, this review paper intends to present feasibility of applying modified zeolite to constructed wetlands which will be beneficial to achieve higher removal effect. [ABSTRACT FROM AUTHOR]

This review is based on the adsorption characteristics of sorghum (Sorghum bicolor) for removal of heavy metals from aqueous media. Different parameters like pH, temperature of the medium, sorghum concentration, sorghum particle size, contact time, stirring speed and heavy metal concentration control the adsorption efficiency of sorghum biomass for heavy metal ions. Sorghum biomass showed maximum efficiency for removal of heavy metal ions in the pH range of 5 to 6. It is an agricultural waste and is regarded as the cheapest biosorbent, having high adsorption capacity for heavy metals as compared to other reported adsorbents, for the treatment of heavy metal polluted wastewater. Adsorption of heavy metal ions onto sorghum biomass follows pseudo second order kinetics. Best fitted adsorption isotherm models for removal of heavy metal ions on sorghum biomass are Langmuir and Freundlich adsorption isotherm models. Thermodynamic aspects of heavy metal ions adsorption onto sorghum biomass have also been elaborated in this review article. How adsorption efficiency of sorghum biomass can be improved by different physical and chemical treatments in future has also been elaborated. This review article will be highly useful for researchers working in the field of water treatment via biosorption processing. The quantitative demonstrated efficiency of sorghum biomass for various heavy metal ions has also been highlighted in different sections of this review article. [ABSTRACT FROM AUTHOR]

This study explores the potential for synchronous extraction of Cu, Cr, Ni and Zn during sewage sludge bioleaching processes, using three types of bacterial cultures: a pure culture of Acidithiobacillus ferrooxidans (A. ferrooxidans); a pure culture of Acidithiobacillus thiooxidans (A. thiooxidans); and a mixed culture of A. ferrooxidans and A. thiooxidans. Variable operating parameters included initial pH, solids concentration, sulfur concentration and ferrous iron concentration, with optimization via Box-Behnken design of response surface methodology. Results indicate that the mixed culture of A. ferrooxidans and A. thiooxidans, was the most effective at bioleaching heavy metals from sewage sludge. The optimal operating conditions were as follows: an initial pH of 2.0, with concentrations of 3% solids, 6.14 g L-1 sulfur and 4.55 g L-1 ferrous iron. Maximum extraction efficiencies obtained after 14 days of bioleaching under optimal conditions, were 98.54% Cu, 57.99% Cr, 60.06% Ni and 95.60% Zn. Bioleaching kinetics were effectively simulated using a shrinking core model to explain the leaching reaction, with modelling results suggesting that the rate was determined by the diffusion step. [ABSTRACT FROM AUTHOR]

In this study, activated carbon (AC) was prepared from walnut shell using chemical activation. The surface chemistry of the prepared AC was modified by introducing or blocking certain functional groups, and the role of the different functional groups involved in the copper uptake was investigated. The structural and chemical heterogeneity of the produced carbons are characterized by Fourier transform infrared spectrometry, X-ray photoelectron spectroscopy, Boehm titration method and N2/77 K adsorption isotherm analysis. The equilibrium and the kinetics of copper adsorption onto AC were studied. The results demonstrated that the functional groups on AC played an important role in copper uptake. Among various surface functional groups, the oxygencontaining group was found to play a critical role in the copper uptake, and oxidation is the most effective way to improve Cu (II) adsorption onto AC. Ion-exchange was identified to be the dominant mechanism in the copper uptake by AC. Some other types of interactions, like complexation, were also proven to be involved in the adsorption process, while physical force was found to play a small role in the copper uptake. The regeneration of copper-loaded AC and the recovery of copper were also studied to evaluate the reusability of the oxidized AC. [ABSTRACT FROM AUTHOR]

Ureido-functionalized mesoporous polyvinyl alcohol/silica composite nanofibre membranes were prepared by electrospinning technology and their application for removal of Pb2+ and Cu2+ from wastewater was discussed. The characteristics of the membranes were investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and N2 adsorptiondesorption analysis. Results show that the membranes have long fibrous shapes and worm-like mesoporous micromorphologies. Fourier transform infrared spectroscopy confirmed the membranes were successfully functionalized with ureido groups. Pb2+ and Cu2+ adsorption behavior on the membranes followed a pseudo-second-order nonlinear kinetic model with approximately 30 minutes to equilibrium. Pb2+ adsorption was modelled using a Langmuir isotherm model with maximum adsorption capacity of 26.96 mg g-1. However, Cu2+ adsorption was well described by a Freundlich isotherm model with poor adsorption potential due to the tendency to form chelating complexes with several ureido groups. Notably, the membranes were easily regenerated through acid treatment, and maintained adsorption capacity of 91.87% after five regeneration cycles, showing potential for applications in controlling heavy metals-related pollution and metals reuse. [ABSTRACT FROM AUTHOR]

Sludge treatment reed bed (STRB) systems combine dewatering, stabilisation and long-term storage of sludge. The main objective of this study was to investigate how substance concentrations change in the sludge residue during treatment and to conduct substance flow analyses covering the flow of substances in an STRB system over a 12-year treatment period, followed by three months' posttreatment in a stockpile area (SPA). Samples of sludge, reject water and sludge residue of different ages were collected at two Danish STRB system facilities and analysed for content of relevant substances. Concentrations of carbon and nitrogen in the sludge residue residing in an STRB system changed as a function of treatment time, mainly due to mineralisation; only a negligible part was lost to reject water. Considering metals and phosphorus, the main share was accumulated in the sludge residue; only minor fractions were lost to mineralisation or reject water. Post-treatment in an SPA resulted in an increase in dry matter content from 24% to 32%. After treatment, the concentrations of heavy metals (lead, cadmium, nickel, zinc, copper and chromium) in the sludge residue met the threshold values stated by the Danish Environmental Protection Agency and the EU. [ABSTRACT FROM AUTHOR]

The present work was aimed at evaluating the multi-metals column adsorption of lead(II), cadmium(II) and manganese(II) ions onto natural bentonite. The bentonite clay adsorbent was characterized for physical and chemical properties using X-ray diffraction, X-ray fluorescence, Brunauer--Emmett--Teller surface area and cation exchange capacity. The column performance was evaluated using adsorbent bed height of 5.0 cm, with varying influent concentrations (10 mg/L and 50 mg/L) and flow rates (1.4 mL/min and 2.4 mL/min). The result shows that the breakthrough time for all metal ions ranged from 50 to 480 minutes. The maximum adsorption capacity was obtained at initial concentration of 10 mg/L and flow rate of 1.4 mL/min, with 2.22 mg/g of lead(II), 1.71 mg/g of cadmium(II) and 0.37 mg/g of manganese(II). The order of metal ions removal by natural bentonite is lead(II) > cadmium(II) > manganese(II). The sorption performance and the dynamic behaviour of the column were predicted using Adams--Bohart, Thomas, and Yoon--Nelson models. The linear regression analysis demonstrated that the Thomas and Yoon--Nelson models fitted well with the column adsorption data for all metal ions. The natural bentonite was effective for the treatment of wastewater laden with multi-metals, and the process parameters obtained from this work can be used at the industrial scale. [ABSTRACT FROM AUTHOR]

The concentrations of eight heavy metals (Cr, Hg, As, Pb, Cd, Cu, Zn, Ni) in six river sediment samples were collected for evaluation of the degree of the heavy metals pollution distribution and ecological risk of three main rivers' sediments in Jinan. Multivariate statistical techniques were used to determine the most common pollution sources. The results illustrated that all of the metals in Damatou and Xinfengzhuang sections of the Xiaoqing River were much higher than the background value, and the level of potential ecological risk index was very high. The remaining four sections had a low or moderate degree of ecological risk. Principal component analysis (PCA) showed that all metals, with the exception of As, formed the first component explaining 86.85% of the total variance and industry sources could be considered as the first component, while As alone could be the second component, representing agricultural source. The elements Cr and Zn were grouped together while the remaining six metals formed a separate category. Among all heavy metals, Hg and Cd were the most significant contributors to the pollution. Therefore, the prevention of pollution should pay more attention to controlling the sources, especially Hg and Cd. [ABSTRACT FROM AUTHOR]

Wastewater from washing, oil separators, the metal processing and detergent industries, was tested and treated for treatment of different types of liquid waste at industrial level at Domžale-Kamnik Wastewater Treatment Plant (WWTP). The effect of implementing the electrocoagulation (EC) and flotation processes, respectively, is analysed and includes the duration of the EC implementation, voltage, number of electrodes, and chemical addition, as well as the pH effect and conductivity. The tests were performed not only on various types of liquid waste, but also on different mixtures of liquid waste. Laboratory analysis of the samples before and after EC have shown an effective reduction not only in organic loads in accordance with the COD (chemical oxygen demand) parameter, but also in mineral oil content, toxic metal concentration, and surfactants. The COD in liquid waste from the detergent industry was reduced by 73% and the content of surfactants by 64%. In liquid waste from the metal processing industry, the COD decreased by up to 95%, while the content of toxic metals decreased from 59 to 99%. Similar phenomena were shown in liquid waste from oil separators, where the COD was reduced to 33% and the concentration of mineral oils by 99%. Some of the liquid wastes were mixed together in the ratio 1:1, thus allowing testing of the operation of EC technology in heterogeneous liquid waste, where the final result proved to be effective cleaning as well. After treatment in the process of EC, the limit values of the treated water proved appropriate for discharge into the sewerage system. [ABSTRACT FROM AUTHOR]

In this study, zeolites were synthesized from low-calcium (LCZ) and high-calcium (HCZ) fly ash, respectively. Subsequently, the zeolites were tested for their removal effectiveness for four aqueous cations, namely, Zn2+, Cu2+, Cd2+, and Pb2+, as a function of contact time, pH value, adsorbent dosage, and initial concentration of heavy metals. Both zeolites were characterized by X-ray diffraction, X-ray fluorescence spectrometry, scanning electron microscopy, specific surface area, and cation exchange capacity. The results show that HCZ mainly consists of an unnamed zeolite (Na6[AlSiO4]6·4H2O), whereas LCZ mainly consists of faujasite-type zeolite. The optimum sorption conditions were pH = 6.0; adsorbent dosage = 1.0 g·L-1; temperature = 25 WC; contact time = 100 min; and initial heavy metal concentration = 100 mg·L-1. The sorption kinetics of the four aqueous cations on both LCZ and HCZ followed the pseudo-second-order kinetic model, and the sorption isotherm data fitted well with the Langmuir isotherm model. For LCZ, the maximum adsorption capacities of Zn2+, Cu2+, Cd2+, and Pb2+ were 155.76, 197.86, 123.76, and 186.22 mg·g-1, respectively. For HCZ, the values were 154.08, 183.15, 118.91, and 191.94 mg·g-1, respectively. The zeolites were regenerated by NaCl solution (1 mol·L-1) and showed high removal efficiency. In conclusion, zeolites produced by fly ash are promising materials for removing Zn2+, Cu2+, Cd2+, and Pb2+ from wastewater. [ABSTRACT FROM AUTHOR]

The black-odor mechanism of Yitong River was analyzed based on survey and monitoring results. We found that organic matter is the main pollution source of Yitong River and its tributaries. A black-odor evaluation model that can describe the pollution of the Yitong River water system was developed, and this model has the parameters I = 0.21 [CODCr] + 0.18 [DO] -- 0.36[NH3-N] + 0.91. The model performance was satisfactory with a black-odor defining accuracy of 69%. Moreover, we found that CODCr, NH3-N, and DO are the influential factors of the Yitong River black-odor water body and that their threshold values when the water body transitioned to black odor were 109.2, 1.90, and 7.50 mg·L-1, respectively. We found that most of the Yitong River was polluted by six heavy metals, namely, As, Cd, Cr, Cu, Pb, and Zn. We used the Nemerow method to calculate the heavy metal pollution degree of each sampling point and found that 60% of the points were seriously polluted. Furthermore, we drew the heavy metal pollution distribution map of the Yitong River. Finally, we proposed an effective measure called new-type multistep constructed wetland to improve the water quality of Yitong River. [ABSTRACT FROM AUTHOR]

The negative effects of heavy metals have aroused much attention due to their high toxicity to human beings. Migration and transformation trend of heavy metals have a close relationship with soil safety. Researching on migration and transformation of heavy metals in tailings can provide a reliable basis for pollution management and ecosystem restoration. Heavy metal speciation plays an important role in risk assessment. We chose Anshan tailings for our study, including field investigations and laboratory research. Four typical heavy metal elements of mine tailings {Fe (373.89 g/kg), Mn (2,303.80 mg/kg), Pb (40.99 mg/kg) and Cr (199.92 mg/kg)} were studied via Tessier test in vertical and horizontal direction. The main speciation of heavy metals in Anshan tailings was the residual. However, heavy metals have a strong ability for migration and transformation in vertical and horizontal directions. Its tendency to change from stable to unstable speciation results in increasing bioavailability and potential bioavailability. Fe, Mn, Pb and Cr showed different ability in the migration and transformation process (Mn>Pb> Fe> Cr) depending on the characteristics of heavy metals and physicochemical properties of the environment. [ABSTRACT FROM AUTHOR]

This study examined the feasibility of nanoscale zero-valent iron (nZVI) for the single and combined removal of Cr(VI) and Cd(II) with or without ethylene diamine disuccinic acid (EDDS). The effects of pH and dissolved oxygen (DO) on the removal process were investigated. Results show that the single removal of either Cr(VI) or Cd(II) by nZVI was pH dependent, where the higher Cr(VI) removal was achieved under acidic conditions, whereas the higher Cd(II) removal was achieved under alkaline conditions. The presence of DO enhanced Cd(II) removal but inhibited Cr(VI) removal under alkaline conditions. In the co-existence of Cr(VI) and Cd(II), it was found that Cd(II) exerted insignificant effect on Cr(VI) removal, while the presence of Cr(VI) remarkably enhanced the Cd(II) removal. The addition of EDDS exhibited different influences on Cr(VI) and Cd(II) removal, which were associated with pH and DO. The EDDS enhanced Cr(VI) removal at pH 5.6-9.0 in the absence of DO, but decreased Cr(VI) removal at pH 9.0 in the presence of DO. For the removal of Cd(II) at pH 5.6-7.0, either facilitation or inhibition effect of EDDS was observed, depending on EDDS concentration and the co-existence of Cr(VI). However, Cd(II) removal was always significantly inhibited by EDDS at pH 9.0. [ABSTRACT FROM AUTHOR]

Lead (Pb2+) is a heavy metal which is utilized in several industries and can have severe impact on the environment and human health. Research work has been carried out lately on the feasibility of using various low cost materials in the removal of heavy metals from wastewater. In this study, the feasibility of utilizing raw rice straw for removal of Pb2+ from water through biosorption was investigated using batch equilibrium experiments. The effect of several operating parameters on the removal of Pb2+ using rice straw was studied, revealing the optimum parameters at an initial Pb2+ concentration of 40 mg/l were: 30 min contact time at a pH of 5.5, particle size 75-150 μm and a dose of 4 g/l. A maximum removal of 94% was achieved under optimum conditions. Langmuir and Freundlich isotherm models were used for the evaluation of the equilibrium experimental data. The maximum adsorption capacity of rice straw calculated using the Langmuir isotherm was 42.55 mg/g. [ABSTRACT FROM AUTHOR]

In 2014, 25% of the sludge produced at Swedish municipal wastewater treatment plants was applied to agricultural land. Even though the Swedish heavy metal limits for sludge to be used in agriculture are amongst the most stringent in the EU, more stringent heavy metal limits are proposed. Most sludge applied to agricultural land is recycled within a certification system, Revaq. Revaq has targets for control at source management and improvement of sludge quality. Statistics based on data collected within the Revaq system was used to differentiate between local and general sources of heavy metals and assess the need to improve sludge quality. The analysis indicates that proposed future national limits on the quality of the sludge can be met by most of the sludge. The improvement needed for about 20% of the sludge is feasible through local control at source management. The levels of cadmium, copper and mercury need to be reduced if these metals are not to limit the amount of sludge that may be applied per unit area of arable land. Finally, the long term Revaq targets for cadmium and silver will be difficult to meet. [ABSTRACT FROM AUTHOR]

The aim of the study was to examine heavy metal tolerance (Cd2+, Zn2+, Ni2+ and Cu2+) of single- and mixed-species biofilms (Rhodotorula mucilaginosa and Escherichia coli) and to determine metal removal efficiency (Cd2+, Zn2+, Ni2+, Cu2+, Pb2+ and Hg2+). Metal tolerance was quantified by crystal violet assay and results were confirmed by fluorescence microscopy. Metal removal efficiency was determined by batch biosorption assay. The tolerance of the mixed-species biofilm was higher than the single-species biofilms. Single- and mixed-species biofilms showed the highest sensitivity in the presence of Cu2+ (E. coli-MIC 4 mg/ml, R. mucilaginosa-MIC 8 mg/ml, R. mucilaginosa/E. coli-MIC 64 mg/ml), while the highest tolerance was observed in the presence of Zn2+ (E. coli-MIC 80 mg/ml, R. mucilaginosa-MIC 161 mg/ml, R. mucilaginosa-E. coli-MIC 322 mg/ml). The mixed-species biofilm exhibited better efficiency in removal of all tested metals than single-species biofilms. The highest efficiency in Cd2+ removal was shown by the E. coli biofilm (94.85%) and R. mucilaginosa biofilm (97.85%), individually. The highest efficiency in Cu2+ (99.88%), Zn2+ (99.26%) and Pb2+ (99.52%) removal was shown by the mixed-species biofilm. Metal removal efficiency was in the range of 81.56%-97.85% for the single- and 94.99%-99.88% for the mixed-species biofilm. [ABSTRACT FROM AUTHOR]

In this paper, the amine-functionalized magnetite hollow nanospheres (AMHNs), prepared through a facile one-pot synthesis, used as heavy metal ions adsorbents, whose morphology and physicochemical features were exploring by transmission electron microscopy, VSM, X-ray diffraction and Fourier-transform infrared analyses. Its adsorption performances for Pb2+, Cu2+, Zn2+, Ni2+ and Cd2+ were studied in detail. The adsorption ameliorated with the increase of initial pH value of the solution and could be affected by ionic strength obviously. Besides, the adsorption kinetics and isothermals were studied. The adsorption processes of Pb2+, Cu2+, Zn2+, Ni2+ and Cd2+ could all reach equilibrium in 60 min and be described well by the Langmuir thermodynamics model. The saturated adsorption capacities of Pb2+, Cu2+, Zn2+, Ni2+ and Cd2+ were 0.66 mmol/g, 0.47 mmol/g, 0.45 mmol/g, 0.38 mmol/g and 0.26 mmol/g, respectively. In addition, the competitive adsorption showed the AMHNs had higher affinity to Pb2+ than to other heavy metal ions. [ABSTRACT FROM AUTHOR]

Implications of three sewer pipe materials (concrete, galvanized corrugated steel, and polyvinyl chloride (PVC)) for stormwater quality were explored in laboratory experiments, in which three types of stormwater, SW1-SW3, were circulated in 0.5 m long sewer pipe sections. SW1 and SW2 represented synthetic rainwater, without and with fine street sediment added (CTSS = 150 mg/L), respectively, and SW3 was actual stormwater with the same sediment addition as SW2. Following 20-min runs, with an equivalent distance of 500 m travelled by water particles, a number of statistically significant changes in the stormwater chemistry were observed: (i) pH of all the simulated stormwaters increased in the concrete pipe (from 7.0-7.3 to 8.1-9.3), (ii) turbidity decreased in two stormwaters with sediments (SW2 and SW3) in concrete and galvanized corrugated steel pipes (by 50 and 85%, respectively), (iii) the type of stormwater affected the observed copper (Cu) concentrations, with Cudiss concentrations as high as 25.3 μg/L noted in SW3 passing through the PVC pipe, and (iv) zinc (Zn) concentrations sharply increased (Zntot = 759-1,406 μg/L, Zndiss = 670-1,400 μg/L) due to Zn elution from the galvanized steel pipe by all three stormwaters. Such levels exceeded the applicable environmental guidelines. [ABSTRACT FROM AUTHOR]

In order to investigate the effect of hydroxypropyl cellulose (HPC), polyvinylpyrrolidone (PVP) and polyethylene glycol (PEG) on adsorbing capacity of nanosorbent Nd-TiO2/GO, Nd-TiO2/HPC/GO, Nd-TiO2/PVP/GO and Nd-TiO2/PEG/GO nanocomposites were synthesized. Studies by Fourier transform infrared spectroscopy confirmed the expected structure and X-ray diffraction results confirmed the formation of crystalline phase of anatase titania and also graphene oxide (GO). Scanning electron microscopy pictures and energy dispersive X-ray spectroscopy analysis showed the formation of Nd-TiO2 nanoparticles. These nanocomposites were used for removal of lead(II) and copper(II) from water and the effective factors on removal were optimized. The results showed that the maximum removal for all three nanocomposites was at pH? 7. The amount of adsorbent and contact time for Nd-TiO2/HPC/GO and Nd-TiO2/PVP/GO nanocomposites was equal to 0.02 g and 20 minutes respectively, but they were equal to 0.01 g and 15 minutes for Nd-TiO2/PEG/GO nanocomposite. Investigating the effect of interfering ions showed they had no considerable effect on removal efficiency. In order to investigate the effect of photocatalytic activity in optimal conditions and in the presence of visible-ultraviolet light, the removal process was performed. The results showed an increase in removal efficiency. Furthermore, the ability of synthesized nanosorbents to decompose organic compounds available in water was confirmed and their energy band gaps were calculated. [ABSTRACT FROM AUTHOR]

The adsorption of a multi-component system of ferrous, chromium, copper, nickel and lead on single, binary and ternary composites was studied. The aim of the study was to investigate whether a ternary composite of clay, Peanut husks (PH) and saw-dust (SD) exhibited a higher adsorption capacity than that of a binary system of clay and SD as well as a single component adsorbent of PH alone. The materials were used in their raw state without any chemical modifications. This was done to retain the cost effective aspect of the naturally occurring adsorbents. The adsorption capacities of the ternary composite for the heavy metals Fe2+, Cr3+, Cu2+, Ni2+ and Pb2+ were 41.7 mg/g, 40.0 mg/g, 25.5 mg/g, 41.5 mg/g and 39.0 mg/g respectively. It was found that the ternary composite exhibited excellent and enhanced adsorption capacity than both a binary and single adsorbent for the heavy metals Fe2+, Ni2+ and Cr3+. Characterization of the ternary composites was done using FTIR, XRD and TGA. Kinetic models and adsorption isotherms were also studied. The pseudo second order kinetic model and the Langmuir adsorption isotherm best described the adsorption mechanisms for the ternary composite towards each of the heavy metal ions. [ABSTRACT FROM AUTHOR]

A chitosan magnetic membrane was prepared in order to confer magnetic properties to the membrane, which could be used for the removal of cations from aqueous solution. The crosslinked magnetic membrane was compared with pristine chitosan membrane in term of stability, morphology and cation adsorption capacity. The fabricated magnetic materials are thermally stable as shown by thermogravimetric curves. The membrane containing nickel magnetic particles (CHNiF-G) shows high thermal stability compared to the other membranes. The Fourier transform infrared spectroscopy showed successful preparation of chitosan magnetic membrane. Scanning electron microscopy micrographs showed the rough surface of the membrane with increased porosity. The prepared chitosan membranes were applied to cations of copper, nickel and lead in dilute aqueous solution. The chitosan membrane showed the following adsorption order for metallic cations: Cu2+>Ni2+>Pb2+, while CHNiF-G showed higher capacity, 3.51 mmol g-1 for copper, reflecting the improvement in adsorption capacity, since the amount of copper on pristine chitosan gave 1.40 mmol g-1. The time required for adsorption to reach to the equilibrium was 6 h for the selected cations using different chitosan membranes. The kinetic study showed that adsorption followed pseudo-second order kinetics. The most commonly used isotherm models, Freundlich, Langmuir and Temkin, were applied to experimental data using linear regression technique. However, The Temkin model fits better to experimental data. [ABSTRACT FROM AUTHOR]

Incineration of sewage sludge is a common practice in many western countries. Gasification is an attractive option because of its high energy efficiency and flexibility in the usage of the produced gas. However, they both unavoidably produce sewage sludge ashes, a material that is rich in phosphorus, but which is commonly landfilled or used in construction materials. With current uncertainty in phosphate rock supply, phosphorus recovery from sewage sludge ashes has become interesting. In the present work, ashes from incineration and gasification of the same sewage sludge were compared in terms of phosphorus extractability using electrodialytic (ED) methods. The results show that comparable recovery rates of phosphorus were achieved with a single ED step for incineration ashes and a sequential combination of two ED steps for gasification ashes, which was due to a higher influence of iron and/or aluminium in phosphorus solubility for the latter. A product with lower level of metallic impurities and comparable to wet process phosphoric acid was eventually obtained from gasification ashes. Thus, gasification becomes an interesting alternative to incineration also in terms of phosphorus separation. [ABSTRACT FROM AUTHOR]

Urban runoff is known to transport a significant pollutant load consisting of e.g. heavy metals, salts and hydrocarbons. Interactions between solid and dissolved compounds, proper understanding of particle size distribution, dissolved pollutant fractions and seasonal variations is crucial for the selection and development of appropriate road runoff treatment devices. Road runoff at an arterial road in Augsburg, Germany, has been studied for 3.5 years. A strong seasonal variation was observed, with increased heavy metal concentrations with doubled and tripled median concentrations for heavy metals during the cold season. Correlation analysis showed that de-icing salt is not the only factor responsible for increased pollutant concentrations in winter. During the cold period, the fraction of dissolved metals was lower compared to the warm season. In road dust, the highest metal concentrations were measured for fine particles. Metals in road runoff were found to show a significant correlation to fine particles SS63 (<63 μm). Therefore, it is debatable whether treatment devices only implementing sedimentation processes provide sufficient removal rates. [ABSTRACT FROM AUTHOR]

This study focuses on the effectiveness of zeolite (10% CF-Z [0.5]) hydrothermally synthesized from waste quartz sand and calcium fluoride (CF) for ammonium ion and heavy metal removal. Zeolite was characterized through powder X-ray diffraction, Fourier-transform infrared spectroscopy, micromeritics N2 adsorption/desorption analysis, and field emission scanning electron microscopy. The effects of CF addition, Si/Al ratio, initial ammonium concentration, solution pH, and temperature on the adsorption of ammonium on 10% CF-Z (0.5) were further examined. Results showed that 10% CF-Z (0.5) was a single-phase zeolite A with cubic-shaped crystals and 10% CF-Z (0.5) efficiently adsorbs ammonium and heavy metals. For instance, 91% ammonium (10 mg L-1) and 93% lead (10 mg L-1) are removed. The adsorption isotherm, kinetics, and thermodynamics of ammonium adsorption on 10% CF-Z (0.5) were also theoretically analyzed. The adsorption isotherm of ammonium and lead on 10% CF-Z (0.5) in single systems indicated that Freundlich model provides the best fit for the equilibrium data, whereas pseudo-second-order model best describes the adsorption kinetics. The adsorption degree of ions on 10% CF-Z (0.5) in mixed systems exhibits the following pattern: lead>ammonium>cadmium> chromium. [ABSTRACT FROM AUTHOR]

The aim of this study was to determine adsorption properties of cuttlebone, cuttlefish bone as dead biomass, for lead(II) and copper(II) from aqueous solutions. Adsorption kinetic, isotherm and effect of pH (in the range of 2.0-7.0) were investigated in a single component batch system at room temperature (25 ±1 °C). The heavy metal adsorption by cuttlebone was relatively rapid and reached equilibrium in 120 min in all the cases. The pseudo-second order rate equation described the adsorption kinetic of both the ions. The adsorption capacities of Pb2+ and Cu2+ were constantly increased by pH and the optimum condition of pH was determined to be 7.0. The Freundlich model was better fitted than other models with the isotherm data, indicating sorption of the metal ions in a heterogeneous surface. According to the Langmuir model, the maximum adsorption capacities of cuttlebone for Pb2+ and Cu2+ were determined to be 45.9 and 39.9 mg/g, respectively. The results indicated cuttlebone as a promising adsorbent for Pb2+ and Cu2+, which presents a high capacity of self-purification in marine environments and also can be used for removal of the metal ions from water and wastewater. [ABSTRACT FROM AUTHOR]

This study aims to investigate the ability of low cost ceramic membrane filtration in removing three common heavy metals namely; Pb2+, Cu2+, and Cd2+ from water media. The work includes manufacturing ceramic membranes with dimensions of 15 by 15 cm and 2 cm thickness. The membranes were made from low cost materials of local clay mixed with different sawdust percentages of 0.5%, 2.0%, and 5.0%. The used clay was characterized by X-ray diffraction (XRD) and X-ray fluorescence analysis. Aqueous solutions of heavy metals were prepared in the laboratory and filtered through the ceramic membranes. The influence of the main parameters such as pH, initial driving pressure head, and concentration of heavy metals on their removal efficiency by ceramic membranes was investigated. Water samples were collected before and after the filtration process and their heavy metal concentrations were determined by chemical analysis. Moreover, a microstructural analysis using scanning electronic microscope (SEM) was performed on ceramic membranes before and after the filtration process. The chemical analysis results showed high removal efficiency up to 99% for the concerned heavy metals. SEM images approved these results by showing adsorbed metal ions on sides of the internal pores of the ceramic membranes. [ABSTRACT FROM AUTHOR]