Showing papers in "Journal of Hazardous Materials in 2008"

Landfill leachate treatment: Review and opportunity

Abstract: In most countries, sanitary landfilling is nowadays the most common way to eliminate municipal solid wastes (MSW). In spite of many advantages, generation of heavily polluted leachates, presenting significant variations in both volumetric flow and chemical composition, constitutes a major drawback. Year after year, the recognition of landfill leachate impact on environment has forced authorities to fix more and more stringent requirements for pollution control. This paper is a review of landfill leachate treatments. After the state of art, a discussion put in light an opportunity and some results of the treatment process performances are given. Advantages and drawbacks of the various treatments are discussed under the items: (a) leachate transfer, (b) biodegradation, (c) chemical and physical methods and (d) membrane processes. Several tables permit to review and summarize each treatment efficiency depending on operating conditions. Finally, considering the hardening of the standards of rejection, conventional landfill leachate treatment plants appear under-dimensioned or do not allow to reach the specifications required by the legislator. So that, new technologies or conventional ones improvements have been developed and tried to be financially attractive. Today, the use of membrane technologies, more especially reverse osmosis (RO), either as a main step in a landfill leachate treatment chain or as single post-treatment step has shown to be an indispensable means of achieving purification.

Metallurgical recovery of metals from electronic waste: a review.

Abstract: Waste electric and electronic equipment, or electronic waste, has been taken into consideration not only by the government but also by the public due to their hazardous material contents In the detailed literature survey, value distributions for different electronic waste samples were calculated It is showed that the major economic driver for recycling of electronic waste is from the recovery of precious metals The state of the art in recovery of precious metals from electronic waste by pyrometallurgical processing, hydrometallurgical processing, and biometallurgical processing are highlighted in the paper Pyrometallurgical processing has been a traditional technology for recovery of precious metals from waste electronic equipment However, state-of-the-art smelters are highly depended on investments Recent research on recovery of energy from PC waste gives an example for using plastics in this waste stream It indicates that thermal processing provides a feasible approach for recovery of energy from electronic waste if a comprehensive emission control system is installed In the last decade, attentions have been removed from pyrometallurgical process to hydrometallurgical process for recovery of metals from electronic waste In the paper, hydrometallurgical processing techniques including cyanide leaching, halide leaching, thiourea leaching, and thiosulfate leaching of precious metals are detailed In order to develop an environmentally friendly technique for recovery of precious metals from electronic scrap, a critical comparison of main leaching methods is analyzed for both economic feasibility and environmental impact It is believed that biotechnology has been one of the most promising technologies in metallurgical processing Bioleaching has been used for recovery of precious metals and copper from ores for many years However, limited research was carried out on the bioleaching of metals from electronic waste In the review, initial researches on the topic are presented In addition, mechanisms and models of biosorption of precious metal ions from solutions are discussed

Heavy metal adsorption onto agro-based waste materials: A review

Abstract: Adsorption has been proved to be an excellent way to treat industrial waste effluents, offering significant advantages like the low-cost, availability, profitability, easy of operation and efficiency. Biosorption of heavy metals from aqueous solutions is a relatively new process that has proven very promising in the removal of contaminants from aqueous effluents. Biosorption is becoming a potential alternative to the existing technologies for the removal and/or recovery of toxic metals from wastewater. The major advantages of biosorption technology are its effectiveness in reducing the concentration of heavy metal ions to very low levels and the use of inexpensive biosorbent materials. Metal adsorption and biosorption onto agricultural wastes is a rather complex process affected by several factors. Mechanisms involved in the biosorption process include chemisorption, complexation, adsorption-complexation on surface and pores, ion exchange, microprecipitation, heavy metal hydroxide condensation onto the biosurface, and surface adsorption.

Technologies for the removal of phenol from fluid streams: a short review of recent developments.

Abstract: The available technologies for the abatement of phenol from water and gaseous streams are briefly reviewed, and the recent advancements summarized. Separation technologies such as distillation, liquid-liquid extraction with different solvents, adsorption over activated carbons and polymeric and inorganic adsorbents, membrane pervaporation and membrane-solvent extraction, have been discussed. Destruction technologies such as non-catalytic, supercritical and catalytic wet air oxidation, ozonation, non-catalytic, catalytic and enzymatic peroxide wet oxidation, electrochemical and photocatalytic oxidation, supercritical wet gasification, destruction with electron discharges as well as biochemical treatments have been considered. As for the abatement of phenol from gases, condensation, absorption in liquids, adsorption on solids, membrane separation, thermal, catalytic, photocatalytic and biological oxidation have also been considered. The experimental conditions and the performances of the different techniques have been compared.

Adsorption of basic dye on high-surface-area activated carbon prepared from coconut husk: equilibrium, kinetic and thermodynamic studies.

Abstract: Adsorption isotherm and kinetics of methylene blue on activated carbon prepared from coconut husk were determined from batch tests. The effects of contact time (1-30 h), initial dye concentration (50-500 mg/l) and solution temperature (30-50 degrees C) were investigated. Equilibrium data were fitted to Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherm models. The equilibrium data were best represented by Langmuir isotherm model, showing maximum monolayer adsorption capacity of 434.78 mg/g. The kinetic data were fitted to pseudo-first-order, pseudo-second-order and intraparticle diffusion models, and was found to follow closely the pseudo-second-order kinetic model. Thermodynamic parameters such as standard enthalpy (DeltaH degrees), standard entropy (DeltaS degrees) and standard free energy (DeltaG degrees) were evaluated. The adsorption interaction was found to be exothermic in nature. Coconut husk-based activated carbon was shown to be a promising adsorbent for removal of methylene blue from aqueous solutions.

Soil washing for metal removal: a review of physical/chemical technologies and field applications.

Abstract: Soil washing is one of the few permanent treatment alternatives to remove metal contaminants from soils. This paper reviews the various technology types and pilot/full-scale field applications of soil washing applicable to soils highly contaminated with heavy metals. The physical separation technologies, the chemical extraction processes and the integrated processes that combine both physical and chemical methods are discussed separately. This paper reviews basic principles, applicability, advantages and limitations, methods of predicting and improving performance of each physical/chemical technology. The discussion is based on a review of 30 recent laboratory investigations and 37 field applications of soil washing systems which have been undertaken, mostly in the US, for the period 1990-2007. This paper also examines and compares the status of soil washing technology for remediation of soils contaminated with metals in the US, in Canada and in Europe.

Advances in science and technology of modern energetic materials: an overview.

Abstract: Energetic materials such as explosives, propellants and pyrotechnics are widely used for both civilian and military explosives applications. The present review focuses briefly on the synthesis aspects and some of the physico-chemical properties of energetic materials of the class: (a) aminopyridine-N-oxides, (b) energetic azides, (c) high nitrogen content energetic materials, (d) imidazoles, (e) insensitive energetic materials, (f) oxidizers, (g) nitramines, (h) nitrate esters and (i) thermally stable explosives. A brief comment is also made on the emerging nitration concepts. This paper also reviews work done on primary explosives of current and futuristic interest based on energetic co-ordination compounds. Lead-free co-ordination compounds are the candidates of tomorrow's choice in view of their additional advantage of being eco-friendly. Another desirable attribute of lead free class of energetic compounds is the presence of almost equivalent quantity of fuel and oxidizer moieties. These compounds may find wide spectrum of futuristic applications in the area of energetic materials. The over all aim of the high energy materials research community is to develop the more powerful energetic materials/explosive formulations/propellant formulations in comparison to currently known benchmark materials/compositions. Therefore, an attempt is also made to highlight the important contributions made by the various researchers in the frontier areas energetic ballistic modifiers, energetic binders and energetic plasticizers.

Photocatalytic degradation of organic dyes with manganese-doped ZnO nanoparticles.

Abstract: Manganese-doped and undoped ZnO photocatalysts were synthesized via wet-chemical techniques. Doping of ZnO with manganese (Mn(2+)) was intended to create tail states within the band gap of ZnO. These can subsequently be used as efficient photocatalysts which can effectively degrade organic contaminants only with visible light irradiation. Photocatalysts prepared with these techniques, which were characterized with transmission electron microscopy (TEM), infrared spectroscopy (FTIR), photo-co-relation spectroscopy (PCS) and UV-vis-spectroscopy showed significant difference in the optical absorption of Mn-doped ZnO. Enhancement in optical absorption of Mn-doped ZnO indicates that it can be used as an efficient photocatalyst under visible light irradiation. The photo-reduction activities of photocatalysts were evaluated using a basic aniline dye, methylene blue (MB) as organic contaminant irradiated only with visible light from tungsten bulb. It was found that manganese-doped ZnO (ZnO:Mn(2+)) bleaches MB much faster than undoped ZnO upon its exposure to the visible light. The experiment demonstrated that the photo-degradation efficiency of ZnO:Mn(2+) was significantly higher than that of undoped ZnO and might also be better than the conventional metal oxide semiconductor such as TiO(2) using MB as a contaminant.

Novel biofiltration methods for the treatment of heavy metals from industrial wastewater

Abstract: Most heavy metals are well-known toxic and carcinogenic agents and when discharged into the wastewater represent a serious threat to the human population and the fauna and flora of the receiving water bodies. In the present review paper, the sources have discussed the industrial source of heavy metals contamination in water, their toxic effects on the fauna and flora and the regulatory threshold limits of these heavy metals. The various parameters of the biofiltration processes, their mechanism for heavy metals removal along with the kinetics of biofilters and its modeling aspects have been discussed. The comparison of various physico-chemical treatment and the advantages of biofiltration over other conventional processes for treatment of heavy metals contaminated wastewater have also been discussed. The applications of genetic engineering in the modification of the microorganisms for increasing the efficiency of the biofiltration process for heavy metals removal have been critically analyzed. The results show that the efficiency of the process can be increased three to six folds with the application of recombinant microbial treatment.

Adsorption of metal ions on lignin

Abstract: This study investigated the adsorption of the heavy metal ions Pb(II), Cu(II), Cd(II), Zn(II), and Ni(II) on a lignin isolated from black liquor, a waste product of the paper industry. Lignin has affinity with metal ions in the following order: Pb(II)>Cu(II)>Cd(II)>Zn(II)>Ni(II). The adsorption kinetic data can be described well with a pseudosecond-order model and the equilibrium data can be fitted well to the Langmuir isotherm. Metal ion adsorption was strongly dependent on pH and ionic strength. Surface complexation modelling was performed to elucidate the adsorption mechanism involved. This shows that lignin surfaces contain two main types of acid sites attributed to carboxylic- and phenolic-type surface groups and the phenolic sites have a higher affinity for metal ions than the carboxylic sites.

Toxicity and biodegradability of imidazolium ionic liquids

Abstract: Several bioassays have been carried out to analyze the toxicity and biodegradability of several imidazolium ionic liquids (ILs) in aqueous phase. The synthetized compounds consist of an imidazolium cation with two alkyl substituents in positions 3 (R1) and 1 (R2) and a counter-ion. The alkyl substituent R1 has been fixed as a methyl group and the effect of the alkyl chain length (C1-C8) of the other substituent (R2) has been tested. Moreover, the influence of diverse counter-ions A- (Cl-, PF6, XSO4-) has been analyzed. Acute toxicity and EC50 values of each compound in the aqueous solution have been determined by using the Microtox standard procedure. Biodegradability of IL has been determined by measuring BOD5 of aqueous samples containing IL and/or D-glucose and the IL residual content and/or d-glucose concentration after this assay. The viability of the microorganisms used in the BOD5 has been related to the ATP in the samples, measured by a bioluminescence assay. All the ILs tested were not biodegradable in the considered conditions. Besides, it was found that the shorter the chain length of side chain R2, the lower the toxic effect is. On the contrary, the anion has a little effect on the IL toxicity.

Equilibrium modeling and kinetic studies on the adsorption of basic dye by a low-cost adsorbent: coconut (Cocos nucifera) bunch waste.

Abstract: In this paper, the ability of coconut bunch waste (CBW), an agricultural waste available in large quantity in Malaysia, to remove basic dye (methylene blue) from aqueous solution by adsorption was studied. Batch mode experiments were conducted at 30 °C to study the effects of pH and initial concentration of methylene blue (MB). Equilibrium adsorption isotherms and kinetics were investigated. The experimental data were analyzed by the Langmuir, Freundlich and Temkin models of adsorption. The adsorption isotherm data were fitted well to Langmuir isotherm and the monolayer adsorption capacity was found to be 70.92 mg/g at 30 °C. The kinetic data obtained at different concentrations have been analyzed using a pseudo-first-order, pseudo-second-order equation and intraparticle diffusion equation. The experimental data fitted very well the pseudo-second-order kinetic model.

Biosorption of lead from aqueous solutions by green algae Spirogyra species: kinetics and equilibrium studies.

Abstract: Biosorption is the effective method for the removal of heavy metal ions from wastewaters. Results are presented showing the sorption of Pb(II) from solutions by biomass of commonly available, filamentous green algae Spirogyra sp. Batch experiments were conducted to determine the biosorption properties of the biomass and it was observed that the maximum adsorption capacity of Pb(II) ion was around 140mgmetal/g of biomass at pH 5.0 in 100min with 200mg/L of initial concentration. Temperature change in the range 20-40 degrees C affected the adsorption capacity and the nature of the reaction was found to be endothermic in nature. Uptake kinetics follows the pseudo-second-order model and equilibrium is well described by Langmuir isotherm. Isotherms have been used to determine thermodynamic parameters of the process, viz., free energy change, enthalpy change and entropy change. Various properties of the algae, as adsorbent, explored in the characterization part were chemical composition of the adsorbent, thermal analysis by TGA, surface area calculation by BET method, surface morphology with scanning electron microscope images and surface functionality by FTIR. FTIR analysis of algal biomass revealed the presence of amino, carboxyl, hydroxyl and carbonyl groups, which are responsible for biosorption of metal ions. The results indicated that the biomass of Spirogyra sp. is an efficient biosorbent for the removal of Pb(II) from aqueous solutions.

Removal of phenol from aqueous solutions by adsorption onto activated carbon prepared from biomass material.

Abstract: Activated carbon derived from rattan sawdust (ACR) was evaluated for its ability to remove phenol from an aqueous solution in a batch process. Equilibrium studies were conducted in the range of 25-200mg/L initial phenol concentrations, 3-10 solution pH and at temperature of 30 degrees C. The experimental data were analyzed by the Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherm models. Equilibrium data fitted well to the Langmuir model with a maximum adsorption capacity of 149.25mg/g. The dimensionless separation factor RL revealed the favorable nature of the isotherm of the phenol-activated carbon system. The pseudo-second-order kinetic model best described the adsorption process. The results proved that the prepared activated carbon was an effective adsorbent for removal of phenol from aqueous solution.

Biosorption mechanism of nine different heavy metals onto biomatrix from rice husk

Abstract: A biomatrix was prepared from rice husk, a lignocellulosic waste from agro-industry, for the removal of several heavy metals as a function of pH and metal concentrations in single and mixed solutions. The biomatrix was characterized using scanning electron microscope and Fourier transform infrared spectroscopy, which indicated the presence of several functional groups for binding metal ions. Different experimental approaches were applied to show mechanistic aspects, especially the role of calcium and magnesium present in the biomatrix in ion exchange mechanism. The ultimate maximum adsorption capacity obtained from the Langmuir isotherm increases in the order (mmol/g): Ni (0.094), Zn (0.124), Cd (0.149), Mn (0.151), Co (0.162), Cu (0.172), Hg (0.18) and Pb (0.28). The sorption of Cr(III) onto biomatrix at pH 2 was 1.0 mmol/g. Speciation of chromium, cadmium and mercury loaded on the biomatrix was determined by X-ray photoelectron spectroscopy. The biomatrix has adsorption capacity comparable or greater to other reported sorbents.

Biosorption of cadmium(II) from aqueous solution by red algae (Ceramium virgatum): equilibrium, kinetic and thermodynamic studies.

Abstract: This study focused on the biosorption of total chromium onto red algae (Ceramium virgatum) biomass from aqueous solution. Experimental parameters affecting biosorption process such as pH, contact time, biomass dosage and temperature were studied. Langmuir, Freundlich and Dubinin-Radushkevich (D-R) models were applied to describe the biosorption isotherms. Langmuir model fitted the equilibrium data better than the Freundlich isotherm. The biosorption capacity of C. virgatum biomass for total chromium was found to be 26.5mg/g at pH 1.5 and 10g/L biomass dosage, 90min equilibrium time and 20 degrees C. From the D-R isotherm model, the mean free energy was calculated as 9.7kJ/mol, indicating that the biosorption of total chromium was taken place by chemisorption. The calculated thermodynamic parameters (DeltaG degrees , DeltaH degrees and DeltaS degrees ) showed that the biosorption of total chromium onto C. virgatum biomass was feasible, spontaneous and exothermic at 20-50 degrees C. Kinetic evaluation of experimental data showed that the biosorption processes of total chromium followed well pseudo-second-order kinetics.

Utilization of steel slag for Portland cement clinker production.

Abstract: The aim of the present research work is to investigate the possibility of adding steel slag, a by-product of the conversion of iron to steel process, in the raw meal for the production of Portland cement clinker. Two samples of raw meals were prepared, one with ordinary raw materials, as a reference sample ((PC) Ref ), and another with 10.5% steel slag ((PC) S/S ). Both raw meals were sintered at 1450 °C. The results of chemical and mineralogical analyses as well as the microscopic examination showed that the use of the steel slag did not affect the mineralogical characteristics of the so produced Portland cement clinker. Furthermore, both clinkers were tested by determining the grindability, setting times, compressive strengths and soundness. The hydration products were examined by XRD analysis at 2, 7, 28 and 90 days. The results of the physico-mechanical tests showed that the addition of the steel slag did not negatively affect the quality of the produced cement.

Reported tailings dam failures. A review of the European incidents in the worldwide context.

Abstract: A detailed search and re-evaluation of the known historical cases of tailings dam failure was carried out. A corpus of 147 cases of worldwide tailings dam disasters, from which 26 located in Europe, was compiled in a database. This contains six sections, including dam location, its physical and constructive characteristics, actual and putative failure cause, sludge hydrodynamics, socio-economical consequences and environmental impacts. Europe ranks in second place in reported accidents (18%), more than one third of them in dams 10-20 m high. In Europe, the most common cause of failure is related to unusual rain, whereas there is a lack of occurrences associated with seismic liquefaction, which is the second cause of tailings dam breakage elsewhere in the world. Moreover, over 90% of incidents occurred in active mines, and only 10% refer to abandoned ponds. The results reached by this preliminary analysis show an urgent need for EU regulations regarding technical standards of tailings disposal.

Comparative adsorption of Cu(II), Zn(II), and Pb(II) ions in aqueous solution on the crosslinked chitosan with epichlorohydrin.

Abstract: The crosslinked chitosans synthesized by the homogeneous reaction of chitosan in aqueous acetic acid solution with epichlorohydrin were used to investigate the adsorptions of three metals of Cu(II), Zn(II), and Pb(II) ions in an aqueous solution. The crosslinked chitosan characterized by 13CNMR, SEM, and elemental analysis, and the effects of pH and anion on the adsorption capacity were carried out. The dynamical study demonstrated that the adsorption process was followed the second-order kinetic equation. The results obtained from the equilibrium isotherms adsorption studies of three metals of Cu(II), Zn(II), and Pb(II) ions by being analyzed in three adsorption models, namely, Langmuir, Freundlich, and Dubinnin-Radushkevich isotherm equations, indicated to be well fitted to the Langmuir isotherm equation under the concentration range studied, by comparing the linear correlation coefficients. The order of the adsorption capacity (Qm) for three metal ions was as follows: Cu2+>Pb2+>Zn2+. This technique for syntheses of the crosslinked chitosans with epichlorohydrin via the homogeneous reaction in aqueous acetic acid solution showed that the adsorptions of three metal ions in aqueous solution were followed the monolayer coverage of the adsorbents through physical adsorption phenomena.

Biosorption of cadmium(II), zinc(II) and lead(II) by Penicillium simplicissimum: Isotherms, kinetics and thermodynamics.

Abstract: The isotherms, kinetics and thermodynamics of Cd(II), Zn(II) and Pb(II) biosorption by Penicillium simplicissimum were investigated in a batch system. The effects of pH, initial metal ions concentration, biomass dose, contact time, temperature and co-ions on the biosorption were studied. Adsorption data were well described by both the Redlich-Peterson and Langmuir model. Chemical ion-exchange was found to be an important process based on free energy value from Dubini-Radushkevich isotherm for all metal ions. The results of the kinetic studies of all metal ions at different temperature showed that the rate of adsorption followed the pseudo second-order kinetics well. The thermodynamics constants DeltaG degrees , DeltaH degrees and DeltaS degrees of the adsorption process showed that biosorption of Cd(II), Zn(II) and Pb(II) ions on Penicillium simplicissimum were endothermic and spontaneous.

Phosphate removal from wastewater using red mud.

Abstract: Red mud, a waste residue of alumina refinery, has been used to develop effective adsorbents to remove phosphate from aqueous solution. Acid and acid-thermal treatments were employed to treat the raw red mud. The effects of different treatment methods, pH of solution and operating temperature on adsorption have been examined in batch experiments. It was found that all activated red mud samples show higher surface area and total pore volume as well as higher adsorption capacity for phosphate removal. The red mud with HCl treatment shows the highest adsorption capacity among all the red mud samples, giving adsorption capacity of 0.58 mg P/g at pH 5.5 and 40 degrees C. The adsorption capacity of the red mud adsorbents decreases with increase of pH. At pH 2, the red mud with HCl treatment exhibits adsorption of 0.8 mg P/g while the adsorption can be lowered to 0.05 mg P/g at pH 10. However, the adsorption is improved at higher temperature by increasing 25% from 30 to 40 degrees C. The kinetic studies of phosphate adsorption onto red mud indicate that the adsorption mainly follows the parallel first-order kinetics due to the presence of two acidic phosphorus species, H(2)PO(4)(-) and HPO(4)(2-). An analysis of the adsorption data indicates that the Freundlich isotherm provides a better fitting than the Langmuir model.

Removal of Pb(II) from aqueous solution by oxidized multiwalled carbon nanotubes.

Abstract: Oxidized multiwalled carbon nanotubes (MWCNTs) were employed as sorbent to study the sorption characteristic of Pb(II) from aqueous solution as a function of contact time, pH, ionic strength, foreign ions, and oxidized MWCNTs' contents under ambient conditions using batch technique. The results indicate that sorption of Pb(II) on oxidized MWCNTs is strongly dependent on pH values, and independent of ionic strength and the type of foreign ions. The removal of Pb(II) to oxidized MWCNTs is rather quickly and the kinetic sorption can be described by a pseudo-second-order model very well. Sorption of Pb(II) is mainly dominated by surface complexation rather than ion exchange. The efficient removal of Pb(II) from aqueous solution is limited at pH 7-10. X-ray photoelectron spectroscopy (XPS) is performed to study the sorption mechanism at a molecular level and thereby to identify the species of the sorption processes. The 3-D relationship of pH, Ceq and q indicates that all the data of Ceq-q lie in a straight line with slope -V/m and intercept C0V/m for the same initial concentration of Pb(II) and same content of oxidized MWCNTs of each experimental data.

Evaluation of zeolite A for the sorptive removal of Cs+ and Sr2+ ions from aqueous solutions using batch and fixed bed column operations

Abstract: Zeolite A was chemically synthesized and evaluated, as inorganic ion exchange material, for the removal of cesium and strontium ions from aqueous solutions in both batch and fixed bed column operations. Batch experiments were carried out as a function of pH, initial ion concentration and temperature. Simple kinetic and thermodynamic models have been applied to the rate and isotherm sorption data and the relevant kinetic and thermodynamic parameters were determined from the graphical presentation of these models. Breakthrough data were determined in a fixed bed column at room temperature (298 K) under the effect of various process parameters like bed depth, flow rate and initial ion concentration. The results showed that the total metal ion uptake and the overall bed capacity decreased with increasing flow rate and increased with increasing initial ion concentrations and bed depth. The dynamics of the ion exchange process was modeled by bed depth service time (BDST) model. The sorption rate constants (K) were found to increase with increase in flow rate indicating that the overall system kinetics was dominated by external mass transfer in the initial part of the sorption process in the column.

Behavior of aluminum electrodes in electrocoagulation process

Abstract: In the present work, electrocoagulation process with aluminum electrodes was investigated. Different operational conditions such as composition of Na(2)SO(4) based solutions, pH and current density were examined in a systematic manner. Their influence on (i) electrode polarization phenomena, (ii) pH evolution during electrolysis and (iii) the amount of Al released (coagulant) was investigated. For this purpose, potentiodynamic tests and electrolyses using different electrochemical cell configurations were conducted. It is mainly found that (i) a minimum Cl(-) concentration of the electrolyte of about 60ppm is required to breakdown the anodic passive film and considerably reduce the cell voltage during electrolysis; (ii) the anodic dissolution efficiency is unit; (iii) the global amount of coagulant (Al(3+)) generated has two origins: electrochemical oxidation of the anode and "chemical" attack of the cathode and (iv) electrolysis with Al electrodes acts as pH neutralization of the electrolytic medium. Taking into account advantage of the pH evolution observed during electrolysis, electrocoagulation tests were performed to treat a synthetic wastewater containing heavy metallic ions (Ni(2+), Cu(2+), Zn(2+)). Removal efficiencies over 98% were reached. Furthermore, our results displayed prominently that an increase of current density notably reduces the treatment duration without inducing a strong increase of the charge loading.

Preparation of titanium dioxide photocatalyst loaded onto activated carbon support using chemical vapor deposition: A review paper

Abstract: Various methods to prepare and characterize TiO2 photocatalyst loaded onto activated carbon (AC) support have been developed over the last decade. This photocatalyst has been used in a variety of investigations, i.e. from water decontamination to direct pollutant degradation in aqueous and gas phase systems using UV irradiation and lately with the assistance of ultrasonic sound waves. Chemical vapor deposition (CVD) method is one of the most promising and well-researched methods for deposition of catalysts onto supports. Given its advantage, from an engineering and fundamental aspect, CVD method also has commercial applications. A detailed search of published reports of these investigations was carried out and analyzed in this paper with focus on CVD techniques, activated carbon support and sonication.

Solid phase extraction of heavy metal ions in environmental samples on multiwalled carbon nanotubes.

Abstract: Multiwalled carbon nanotubes (MWNTs) were used as solid phase extractor for Cu(II), Cd(II), Pb(II), Zn(II), Ni(II) and Co(II) ions as ammonium pyrrolidine dithiocarbamate (APDC) chelates, in the present study. The influences of the experimental parameters including pH of the solutions, amounts of MWNTs, amounts of APDC, eluent type and volume, sample volume etc. on the quantitative recoveries of analyte ions were investigated. The effects of matrix ions of natural waters and some transition metals on the recoveries of the analyte ions were also examined in the model solutions. Tests of addition/recovery for analyte ions in real samples were performed with satisfactorily results. The detection limits (3s) for the analyte ions were in the range of 0.30-0.60 microg l(-1). The concentrations of analytes in standard reference materials (NIST RM 8418 Wheat gluten, LGC 6010 Hard drinking water and NIST SRM 1515 Apple leaves) pretreated by the presented method were measured with FAAS and the analytical values were well agreed with the certified values and the reference values without the interference of major components. The presented method has been applied to the determination of analytes in food and environmental samples with satisfactory results.

Adsorption isotherm models for dye removal by cationized starch-based material in a single component system: Error analysis

Abstract: This article describes the adsorption of an anionic dye, namely C.I. Acid Blue 25 (AB 25), from aqueous solutions onto a cationized starch-based adsorbent. Temperature was varied to investigate its effect on the adsorption capacity. Equilibrium adsorption isotherms were measured for the single component system and the experimental data were analyzed by using Langmuir, Freundlich, Tempkin, Generalized, Redlich-Peterson, and Toth isotherm equations. Five error functions were used to determine the alternative single component parameters by non-linear regression due to the bias in using the correlation coefficient resulting from linearization. The error analysis showed that, compared with other models, the Langmuir model described best the dye adsorption data. Both linear regression method and non-linear error functions provided the best-fit to experimental data with the Langmuir model.

Environmental, physical and structural characterisation of geopolymer matrixes synthesised from coal (co-)combustion fly ashes

Abstract: The synthesis of geopolymer matrixes from coal (co-)combustion fly ashes as the sole source of silica and alumina has been studied in order to assess both their capacity to immobilise the potentially toxic elements contained in these coal (co-)combustion by-products and their suitability to be used as cement replacements. The geopolymerisation process has been performed using (5, 8 and 12 M) NaOH solutions as activation media and different curing time (6-48 h) and temperature (40-80 degrees C) conditions. Synthesised geopolymers have been characterised with regard to their leaching behaviour, following the DIN 38414-S4 [DIN 38414-S4, Determination of leachability by water (S4), group S: sludge and sediments. German standard methods for the examination of water, waste water and sludge. Institut fur Normung, Berlin, 1984] and NEN 7375 [NEN 7375, Leaching characteristics of moulded or monolithic building and waste materials. Determination of leaching of inorganic components with the diffusion test. Netherlands Normalisation Institute, Delft, 2004] procedures, and to their structural stability by means of compressive strength measurements. In addition, geopolymer mineralogy, morphology and structure have been studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR), respectively. It was found that synthesised geopolymer matrixes were only effective in the chemical immobilisation of a number of elements of environmental concern contained in fly ashes, reducing (especially for Ba), or maintaining their leachable contents after the geopolymerisation process, but not for those elements present as oxyanions. Physical entrapment does not seem either to contribute in an important way, in general, to the immobilisation of oxyanions. The structural stability of synthesised geopolymers was mainly dependent on the glass content of fly ashes, attaining at the optimal activation conditions (12 M NaOH, 48 h, 80 degrees C) compressive strength values about 60 MPa when the fly ash glass content was higher than 90%.

Application of response surface methodology for optimization of lead biosorption in an aqueous solution by Aspergillus niger

Abstract: Response surface methodology was applied to optimize the removal of lead ion by Aspergillus niger in an aqueous solution. Experiments were conducted based on a rotatable central composite design (CCD) and analyzed using response surface methodology (RSM). The biosorption process was investigated as a function of three independent factors viz. initial solution pH (2.8-7.2), initial lead concentration (8-30 mg/l) and biomass dosage (1.6-6 g/l). The optimum conditions for the lead biosorption were found to be 3.44, 19.28 mg/l and 3.74 g/l, respectively, for initial solution pH, initial lead ion concentration and biomass dosage. Lead biosorption capacity on dead A. niger fungal biomass was enhanced by pretreatment using NaOH. Under these conditions, maximum biosorption capacity of the biomass for removal of lead ions was obtained to 96.21%. The desirability function was used to evaluate all the factors and response in the biosorption experiments in order to find an optimum point where the desired conditions could be obtained. The A. niger particles with clean surface and high porosity may have application as biosorbent for heavy metal removal from wastewater effluents.

Extraction of extracellular polymeric substances from aerobic granule with compact interior structure.

Abstract: Extracellular polymeric substances (EPS) were extracted from aerobic granules of compact interior structure using seven extraction methods. Ultrasound followed by the chemical reagents formamide and NaOH outperformed other methods in extracting EPS from aerobic granules of compact interior. The collected EPS revealed no contamination by intracellular substances and consisted mainly of proteins, polysaccharides, humic substances and lipids. The quantity of extracted proteins exhibited a weak correlation with quantity of extracted carbohydrates but no correlation with quantity of extracted humic substances. The total polysaccharides/total proteins (PN/PS) ratios for sludge flocs were approximately 0.9 regardless of extraction method. Protein content was significantly enriched in the granules, producing a PN/PS ratio of 3.4-6.2. This experimental result correlated with observations using excitation-emission matrix (EEM) and confocal laser scanning microscope technique. However, detailed study disproved the use of EEM results as a quantitative index of extracted EPS from sludge flocs or from granules.