Immobilization of copper under an acid leach of colloidal pyrite waste rocks by a fixed-bed column

Colloidal pyrite waste rocks (CPWR) which are mainly composed of colloidal pyrite and siderite widely deposit in sulfide mines in the middle and lower reaches of the Yangtze River belt, China, especially in Tongling City, Anhui Province, China. In this paper, a fixed-bed column was used to investigate the weathering and oxidation of CPWR and its role in immobilizing low-concentration Cu (10 mg L^?1) under weakly acidic leach (pH = 5.0). The experimental results indicated that the breakthrough capacity was around 14.0 mg Cu g^?1 CPWR when Cu²⁺ breakthrough concentration was 0.5 mg L^?1. Sequential extraction of Cu and dithionite–citrate–bicarbonate extraction of free iron in the used CPWR after the column breakthrough indicated that Cu removal by CPWR consisted of the following processes: oxidation of pyrite and dissolution of siderite in CPWR, ferrous oxidation, and adsorption of Cu on ferric (hydr)oxides. This study shows the potential application of CPWR as an effective sorbent for the removal of low-concentration Cu from acid mine drainage.     

Non-woven polypropylene fabric modified with carbon nanotubes and decorated with nanoakaganeite for arsenite removal

Due to its harmful impact on human health, the presence of heavy metals, metalloids and other toxic pollutants in drinking or irrigation water is a major concern. Recent studies have proved that nanosized adsorbents are significantly more effective than their microsized counterparts. Particular attention has been given to nanocomposites with nanoadsorbents embedded in matrixes that could provide stability to the material and contribute to eliminating problems that may appear when using conventional granular systems. This study presents the preparation of a novel hybrid filter from a commercially available polypropylene (PP) non-woven fabric matrix modified with multiwall carbon nanotubes (MWCNT) and iron oxy(hydroxide) nanoparticles, and its use in the removal of As(III). A Box–Behnken statistical experimental design has been chosen to explore relevant variables affecting the filter performance: (1) As(III) concentration, (2) pH and (3) sorbent dose. From an As(III) concentration of 10 mg L^?1, at pH 6.5 and with a sorbent dose of 5 g L^?1, the PP filter modified with MWCNT removes 10% of the initial metalloid concentration, reaching a capacity of 0.27 mg g^?1. After modification with iron oxy(hydroxide), the performance of the material is largely enhanced. The filter, under the same conditions, removes 90% of the initial As(III) concentration, reaching a capacity almost tenfold higher (2.54 mg g^?1). This work demonstrates that the developed hybrid filter is effective toward the removal of As(III) in a wide range of pHs. A cubic regression model to compute the removal of the filter as a function of pH and sorbent dose is provided.     

Investigation on the effective remediation of quinoline at solid/solution interface using modified agricultural waste: an inclusive study

This research work explores the potential of modified agricultural waste for the sorption of quinoline from aqueous media. A quinoline removal efficiency of around 97 % and sorption capacities of ~20 (batch) and ~35 mg g^?1 (fixed-bed) were achieved. Pseudo-second-order kinetics and Temkin isotherm best represented the equilibrium sorption data. The sorption of quinoline is exothermic and spontaneous in nature with a slight increase in the system entropy. The quinoline sorption mechanism is controlled by H-bonding, π–π dispersive interactions, boundary layer, and intraparticle diffusion. Microwave–chemical integrated regeneration technique retrieves the sorption capacity of the exhausted sorbent with 99.15, 97.64, and 95.55 % of the original, in three sorption–regeneration cycles. Energy recovery (19.365 MJ kg^?1) from the quinoline-loaded sorbent and the potential utilization of left-over ash materials enhanced the prospective of the sorbent for the remediation of pollutants for a clean and green environment.     

Kinetic and equilibrium studies on the removal of <Superscript>14</Superscript>C-ethion residues from wastewater by copper-based metal–organic framework

There are compelling economic and environmental reasons to remove pesticides from wastewater because they are toxic and carcinogenic. The effectiveness of copper-based metal–organic framework (Cu-BTC) for adsorbing the insecticide ¹⁴C-ethion from wastewater has been studied as function of contact time, adsorbent dosage, temperature and pH. ¹⁴C-ethion/Cu-BTC isotherms exhibit two plateaus (BET type IV) and are reliably represented by Brunauer–Deming–Deming–Teller and Zhu–Gu models, with deviations of only 1.99 and 3.95%, respectively. The removal curve measured under batch operation is well represented by a pseudo-first-order equation, yielding results equivalent to the theoretical linear driving force model of Glueckauf. At pH 7, 75 mg L^?1 ethion concentration, 150 min, 25 °C and 0.425 g L^?1 Cu-BTC dose, the sorbent capacity is ca. 122 mg g^?1. Moreover, Cu-BTC has a good stability after six adsorptions cycles. Finally, our results disclose the fundamental understanding of the adsorption mechanism: the ethion molecule coordinates to two copper(II) atoms across the metal–organic framework channel via the phosphoryl (P–O) group.     

Adsorption studies for the simultaneous removal of arsenic and selenium using naturally prepared adsorbent materials

The adsorption properties of eggshell membranes (ESM), eggshells (ES) and orange peels (OP) were studied for the removal of arsenic (total As) and selenium (total Se). The effect of chemical treatment of these adsorbents by HNO₃ and NaOH was also investigated using Fourier transform infrared spectroscopy (FT-IR). Analysis of the FT-IR spectra showed that treatment with NaOH and HNO₃ had an effect on the functional groups present in the materials and also on the adsorption by extension. Thermal analysis showed that ES were more thermally stable than the others with no water molecules in their matrix, which could have caused a substantial weight loss at around 70 °C. In terms of adsorption capacities, chemical treatment increased the adsorption capacities of ESM and OP achieving up to 170 μg g^?1 (As) and 160 μg g^?1 (Se), and 120 μg g^?1 (As) and 70 μg g^?1 (Se), respectively, with not much activity for ES in terms of adsorption. The two adsorbents (NaOH-treated OP and ESM) were then tested in environmental water samples and the results showed that 68.9 % of As and 74.8 % of Se, and 54.1 % of As and 47.3 % of Se were removed from domestic wastewater samples investigated using OP and ESM, respectively. Moreover, better selectivities towards the compounds of interest were achieved.     

Lead removal from aqueous solution by basaltic scoria: adsorption equilibrium and kinetics

Pb-contaminated water is a dangerous threat occurring near metallurgic and mining industries. This circumstance produces serious environment concern, due to Pb(II) high toxic effects. Several reactive materials have been reported for Pb(II) adsorption, but not all reached final Pb(II) suitable concentrations, or they are expensive and rejected in massive remediation technologies; hence, natural materials are good options. The adsorption behavior of a volcanic scoria (two sieved fractions 1425 and <425 µm) was studied toward synthetic Pb(II) water solutions in batch experiments (170.4–912.3 mg L^?1) with high removal efficiencies (97%). The Langmuir model fits both fractions with high linear correlation coefficients (0.9988 and 0.9949) with high maximum capacity values (588.23 and 555.55 mg g^?1). Separation factor R _L parameter varies with initial concentration, and the empirical equation predicts the limits of the material usefulness, a criterion proposed in this paper for conditions’ selection. The Lagergren pseudo-second-order analysis demonstrates chemisorption; calculated rate constant (416.66 mg g^?1 min^?1). Weber–Morris intraparticle model proves that the adsorption phenomena occur fast on the material surface (k _inst = 72 g mg^?1 min^?0.5). The characterization of the volcanic material afforded the elemental composition (X-ray fluorescence), and the empirical formula was proposed. X-ray diffraction patterns verify the material structure as basalt, with a plagioclase structure that matches anorthite and albite, mostly composed of quartz. The presence of oxides on the material surface explain the high Pb(II) adsorption capacity, observed on the surface by scanning electronic microscopy. The studied volcanic scoria has potential use as a Pb(II) adsorbent in water remediation technologies.     

Characterization and evaluation of a tropical peat for the removal of Cr(VI) from solution

Tropical peat soils present higher ash content than those generated at temperate climate areas. Therefore, this study evaluated the characteristics of a Brazilian organic soil (OS), commercialized as peat, as well as its capacity in removing Cr(VI) from contaminated waters. The OS is composed of 35.5 wt% of organic matter and 56 wt% of inorganic fraction (ash), which is formed by minerals and phytoliths rich in silica (29.2 wt%) and alumina (23.6 wt%). The Cr(VI) removal tests were carried out in batch and column systems using OS and solutions of Cr(VI) prepared with distilled water and groundwater. Batch tests revealed that the organic substances in the OS caused the reduction of Cr(VI) to Cr(III), with an efficiency depending on solution pH. At pH 5.0 the Cr(VI) removal was 0.45 mg g^?1 in 24 h; whereas at pH 2.0, this removal increased to 1.10 mg g^?1. Since this redox reaction is very slow, the removal of Cr(VI) at pH 5.0 increased to around 2 mg g^?1 after 5 days. The removal of Cr(VI) was more effective in the column tests than in the batch test due to the greater solid/solution ratio, and their half-lives were 4.4 and 26.2 h, respectively. Chemical analysis indicated that Cr(VI) was reduced by the humic substances of OS, followed by the precipitation and/or adsorption of Cr(III) into the organic and inorganic components, as anatase. The presence of Cr(III) increased the stability of anatase structure, avoiding its transformation into rutile, even after being heated at 800 °C/2 h.     

Removal of chromate from wastewater using amine-based-surfactant-modified clinoptilolite

This study presents the results of chromate adsorption upon organically modified clinoptilolite obtained by the treatment of Bigadic clinoptilolite with surfactants in primary amine structure, namely 1-dodecylamine, 1-hexadecylamine and oleylamine. Natural and organo-clinoptilolites were characterized by X-ray diffraction, thermal gravimetry and Fourier transform infrared spectrometry which proved the integration of amine groups followed by the order oleylamine > 1-hexadecylamine > 1-dodecylamine. Organo-clinoptilolites were tested for their efficacy in chromate removal under base case conditions which implied 100 ppm initial concentration, pH 4.0, 10 g l^?1 adsorbent dose and at 298 K. Results showed that amine loading induced chromate removal reaching up to 90 % for oleylamine-modified clinoptilolite. Experimentation was continued to determine the effects of pH, adsorbent dosage and initial concentration on chromate adsorption. Accordingly, maximum removal of 94.0 % was attained with 14 g l^?1 of oleylamine-modified clinoptilolite, from Cr(VI) solution of 100 ppm initially at pH 3.0. Langmuir isotherm described the adsorption of chromate on oleylamine-modified clinoptilolite with 96.4 % consistency. Maximum theoretical uptake capacity was calculated as 6.72 mg g^?1. Kinetic data were consistent with pseudo-second-order model with the controlling steps being film and pore diffusions.     

The use of multivariate statistical analysis of geochemical data for assessing the spatial distribution of soil contamination by potentially toxic elements in the Aljustrel mining area (Iberian Pyrite Belt,Portugal)

Aljustrel mine is located in SW Portugal, in the western sector of the Iberian Pyrite Belt. The Aljustrel village was developed around the exploitations of massive polymetallic sulphides that occur in the area (4 orebodies mined, 2 in exploration phase). The pyrite ore was extensively exploited from 1850 to 1993, when production was discontinued. A mining restart occurred in 2008, only during a few months. The objectives of the study were to assess the levels of soil contamination, to determine associations between the different chemical elements and their spatial distribution, as well as to identify possible sources of contamination that can explain the spatial patterns of soil pollution in the area. Principal component analysis combined with spatial interpretation successfully grouped the elements according to their sources and provided evidence about their geogenic or anthropogenic origin. From this study, it is possible to conclude that soils around Algares/Feitais tailing deposits, Estéreis and Águas Claras mine dams and S. João mine show severe contamination. The highest concentrations of As (up to 3,936 mg kg^?1) and certain heavy metals (up to 321.7 mg kg^?1 for Bi, 5,414 mg kg^?1 for Cu, 20,000 mg kg^?1 for Pb, 980.6 mg kg^?1 for Sb, and 22 mg kg^?1 Cd) were obtained near Algares area while the highest concentration of Cd (up to 61.6 mg kg^?1) and Zn (up to 20,000 mg kg^?1) were registered in samples collected in the S. João area. The highest pollution load index (>4.0) was recorded at the Algares area where the metal concentrations exceed typical soil background levels by as much as two orders of magnitude.     

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

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

Changes in water chemistry along the newly formed High Arctic fluvial–lacustrine system of the Brattegg Valley (SW Spitsbergen,Svalbard)

Changes in water chemistry along the High Arctic fluvial–lacustrine system located in Wedel Jarlsberg Land in the SW Spitsbergen (Svalbard) were investigated during the summer season of 2010 and 2011. The newly formed river–lake system consists of three lakes connected with the Brattegg River. The first bathymetric measurements of these lakes were made by the authors in 2010. The Brattegg River catchment represents a partly glaciered Arctic water system. The studied lakes are characterized by low mineralization and temperature of water. The value of the electrolytic conductivity (EC) ranges from 30.2 to 50.5 μS cm^?1 and the temperature of surface water from 1.5 to 7.8 °C. The temperature increase takes place downstream starting from Upper Lake to the outflow from Myrktjørna Lake. The waters of lakes have higher temperatures than the stream. The predominant ions are HCO₃ ^? (up to 16.5 mg L^?1), Cl^? (6.66–8.53 mg L^?1), Ca²⁺ (2.40–4.45 mg L^?1) and Na⁺ (2.65–3.36 mg L^?1). The highest values of ammonium and DOC found in the lowest Myrktjørna Lake seem to be related to the presence of aquatic organisms and also birds. From the group of 10 analyzed microelements, increased concentrations of aluminum, up to almost 500 μg L^?1, are present in the lakes’ water. Water isotopic composition ranges for δ¹⁸O and δ²H, from ?10.6 to ?10.9‰ and from ?70.8 to ?72.3‰, respectively. The vertical zonality of lake waters is manifested in a decrease in the temperature and increase in EC and chemical elements concentrations.     

Biosorption optimization and equilibrium isotherm of industrial dye compounds in novel strains of microscopic fungi

The aim of this study was to evaluate the biosorption capacity of selected strains of microscopic fungi. We optimized the biosorption process and used the Freundlich isotherm for three strains: H. haematococca BwIII43, K37 and T. harzianum BsIII33 to describe the biosorption equilibrium of anthraquinone dye, Alizarin Blue Black B (ABBB) and alkali lignin (AL). In optimal conditions (1 g of mycelium biomass, pH = 7.0, 28 °C) for ABBB and AL sorption, the live biomass of H. haematococca BwIII43 was characterized by a higher sorption capacity, amounting to 247.47 and 161.00 mg g^?1, respectively. The highest sorption properties toward anthraquinone dye (K _F = 19.96 mg g^?1) were shown for the biomass of H. haematococca K37. In the presence of alkali lignin, the highest sorption capacity and bond strength exhibited the biomass of H. haematococca BwIII43 (K _F = 28.20 mg g^?1, n = 3.46). Effective decolorization of ABBB and AL by the selected strains of microscopic fungi indicated that the biosorption process additionally enhanced the removal of color compounds from the solution.     

<Emphasis Type="Italic">Inoculum</Emphasis>-free start-up of biofilm- and sludge-based deammonification systems in pilot scale

Undiluted reject water from the dewatering of anaerobic sludge with an average total nitrogen content of 718 ± 117 mg L^?1 (n = 63) was used to start-up autotrophic nitrogen removal in three different pilot-scale (3 m³) deammonification configurations: (1) biofilm; (2) activated sludge sequence batch; and (3) two-staged (nitritation–anammox). Time- and concentration-based aeration control with alternating aerobic/anaerobic phases was applied for all reactor configurations. All reactors were initiated without anammox-specific inoculum, and biofilm was grown onto blank carriers. During the initial start-up period, biological nitrogen removal was found to be inhibited by an excessive free ammonia content (>10 mg-N L^?1), resulting from the use of high-strength reject water as the process feed. After implementation of free ammonia control by pH adjustment to 6.5–7.5, propagation of the deammonification process was observed with increased nitrogen removal with slight accumulation of NO₃ ^?–N. The highest total nitrogen removal rates were achieved with the single-reactor biofilm- and sludge-based deammonification processes (1.04 and 0.30 kg-N m^?3 day^?1, respectively). The critical factors for successful start-up and stable operation of deammonification reactors turned out to be control of pH below 7.5, dissolved oxygen at 0.3–0.8 mg-O₂ L^?1 and influent solids values below 1000 nephelometric turbidity units. Microbial analysis demonstrated that highest anammox enrichment was achieved in the biofilm reactor (9.40 × 10⁸ copies g^?1 total suspended solids). These data demonstrate the potential of an in-situ grown sludge- or biofilm-based concept for the development and propagation of deammonification process.     

Efficiency assessment of aerobic biological effluent treatment plant treating pharmaceutical effluents

The present paper undertakes a study of the physico-chemical properties and toxic heavy metals content in the untreated and treated pharmaceutical effluents in order to evaluate the working efficiency of industrial effluent treatment plants. The treatment efficiency achieved for various parameters was conductivity (79.94%), alkalinity (93.91%), hardness (87.70%), chloride (89.24%), cyanide (79.66%), phosphate (99.19%), total dissolved solids (85.89%), total suspended solids (96.87%), salinity (52.41%), dissolved oxygen (27.32%), biochemical oxygen demand (83.39%) and chemical oxygen demand (72.21%). The removal efficiency achieved for different heavy metals was Cu²⁺ (79.66%), Ni²⁺ (69.22%), Cr⁶⁺ (80.15%), Pb²⁺ (72.14%), Fe³⁺ (92.59%) and Zn²⁺ (90.61%). The level of biochemical oxygen demand (64 mg L^?1) in the treated effluents was above the limit of 30.0 mg L^?1, chemical oxygen demand level (208 mg L^?1) was close to a limit of 250 mg L^?1, while average Pb²⁺ concentration (0.10 mg L^?1) was on the borderline of maximum permissible limit of 0.10 mg L^?1 set by Central Pollution Control Board for safe discharge of industrial effluent in inland surface water. The average concentration of cyanide (0.01 mg L^?1) in the treated industrial effluent of our study is of great concern to the fisheries of freshwater ecosystem in which the effluents finally get discharged. Based on the results of the present study, it is concluded that the pollution level in the discharged pharmaceutical effluent is of the great concern requiring proper treatment and regular scientific monitoring so as to protect the environmental degradation of water resources and facilitate the propagation of the aquatic life.     

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

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

Isolation of <Emphasis Type="Italic">Virgibacillus</Emphasis> sp. strain KU4 from agricultural soil as a potential degrader of endocrine disruptor bisphenol-A

Bisphenol-A is one of the highest volumes of chemicals produced worldwide and released into the atmosphere each year. Recent extensive literature has raised concerns about its possible endocrine-disrupting effect in animals and humans. A bacterium having high tolerance of bisphenol-A (1000 mg L^?1) was isolated from agriculture soil of Coimbatore District, Tamil Nadu, India, and identified as Virgibacillus sp. KU4 by 16S ribosomal RNA sequence analysis. Bisphenol-A removal efficiency of this strain was measured as greater than 92% at seventh day of incubation in a basal mineral medium supplemented with 1000 mg L^?1 at seventh day. Gas chromatography analysis showed that 1000 mg L^?1 BPA in distilled water was degraded by the Virgibacillus sp. KU4 in an efficient way. A 70 ± 3% bisphenol-A degradation was observed in the suspended cell pellet-mediated degradation study, where distilled water supplemented with 1000 mg L^?1 bisphenol-A was sole carbon and energy source for bacterial growth. Further, Virgibacillus sp. KU4 is expected to be a candidate as a biological cleaner of BPA in the environment.     

Uptake of Indosol Dark-blue GL dye from aqueous solution by water hyacinth roots powder: adsorption and desorption study

Adsorption characteristics of water hyacinth roots powder for the removal of Indosol Dark-blue GL dye were investigated in batch mode. Operating variables, such as initial solution pH, presence of detergent, adsorbent dosage, initial concentration and contact time, were studied. The results showed that the adsorption of dye increased with increasing the initial concentration and contact time. The adsorption is highly pH dependent and adsorption capacity increased with decrease in pH. Kinetic study revealed that the uptake of Indosol Dark-blue GL was very rapid within the first 15 min and equilibrium time was independent of initial concentration. Batch equilibrium experiments were carried out at different pH and found that equilibrium data fitted well to Langmuir isotherm model. The maximum sorption capacity of the adsorbent was found as 86 mg g^?1 at pH 3 which reduced to 64 mg g^?1 at pH 5. The presence of detergent reduced the sorption capacity of the adsorbent significantly. Using equilibrium and kinetic data, the forward and backward rate constants were determined from the unified approach model. Desorption study revealed that the dye can be recovered by swing the pH from low to high.     

Efficient removal of hexavalent chromium from aqueous solutions using autohydrolyzed Scots Pine (Pinus Sylvestris) sawdust as adsorbent

In this work, a low-cost lignocellulosic adsorbent with high biosorption capacity is proposed, suitable for the efficient removal of hexavalent chromium from water and wastewater media. The adsorbent was produced by autohydrolyzing Scots Pine (Pinus Sylvestris) sawdust. The effect of the autohydrolysis conditions, i.e., pretreatment time and temperature, on hexavalent chromium biosorption was investigated using energy-dispersive X-ray spectroscopy (EDS) and UV–visible spectrophotometry. The Freundlich, Langmuir, Sips, Radke-Prausnitz, Modified Radke-Prausnitz, Tóth, UNILAN, Temkin and Dubinin-Radushkevich adsorption capacities and the rate constant values for pseudo-first- and pseudo-second-order kinetics indicated that the autohydrolyzed material exhibits significantly enhanced hexavalent chromium adsorption properties comparing with the untreated sawdust. The Freundlich’s adsorption capacity K _F increased from 2.276 to 8.928 (mg g^?1)(L mg^?1)^1/n , and the amount of hexavalent chromium adsorbed at saturation (Langmuir constant q _m) increased from 87.4 to 345.9 mg g^?1, indicating that autohydrolysis treatment at 240 °C for 50 min optimizes the adsorption behavior of the lignocellulosic material.     

Phytoremediation assessment of native plants growing on Pb–Zn mine site in Northern Tunisia

Pollution by heavy metals presents an environmental concern, and their toxicity threats soil, water, animals and human health. Phytoremediation can be used as a solution to remediate contaminated soils. The aim of this study was to identify native plants collected from tailings: material of Pb–Zn mine sites of Fedj Lahdoum and Jebel Ressas (two abandoned mines located, respectively, in the northwest of Tunisia and in the south of Tunis City). The tolerance of plant to heavy metals (lead, zinc and cadmium) is evaluated. Soil samples were collected and analyzed for Pb, Zn and Cd concentration. The total soil Pb, Zn and Cd are, respectively, reached 6132 mg kg^?1, 11,052 mg kg^?1 and it doesn’t exceed 479 mg kg^?1 for Cd. The highest content of Zn in plants was detected in shoots of Rumex bucephalophorus (1048 mg kg^?1), and the highest Pb concentration was detected in roots of Chrysopogon zizanioides (381 mg kg^?1), while for Cd Silene colorata it accumulated the highest content in roots (51 mg kg^?1). From all plants, only 12 have a translocation factor for Pb which is higher than one. Among all plants, only 17 have a translocation factor that is higher than one for Zn, while for Cd only 13 plants indicate TF > 1. As for the biological absorption coefficient, all samples indicate a rate which is lower than one. These plants can be primarily hyper accumulators and useful in remediation of lead- and zinc-contaminated soils after further biochemistry researches in mechanism of accumulation and translocation of heavy metals in plants.     

Evaluating the production and bio-stimulating effect of 5-methyl 1, hydroxy phenazine on microbial fuel cell performance

The role of endogenous redox mediators has considerable importance in electron shuttling reactions and associated performance of microbial fuel cell. Single-chamber microbial fuel cell-II with dual air-cathode assembly (area = 18.84 cm²) supported highest bacterial (Pseudomonas aeruginosa) density (6.7 × 10⁹) and active biomass [4.4 ± 0.3 mg cm^?2 (carbon content = 0.48 ± 0.1 mg cm^?2)] on anode thereby resulting in maximum production of redox metabolite, 5-methyl 1, hydroxy phenazine (301 ppm) and voltage (595 ± 5 mV) than similar cells with relatively less surface area of cathode. It was further revealed that 5-methyl 1, hydroxy phenazine production was positively correlated with chemical oxygen demand removal rate (77 ± 2.5%) and power generation (66.6 ± 2.2 mW cm^?2) efficiency of single-chamber microbial fuel cell-II. Maximum power density of 258 ± 4.5 mW cm^?2 was generated when reactor was supplemented with 2 ml crude extract of 5-methyl 1, hydroxy phenazine metabolite, whereas power output was about 229 ± 2.5 mW cm^?2 when reactor was bio-stimulated with 1 ml pure extract of 5-methyl 1, hydroxy phenazine. With this concentration, the electrochemical response of mixed culture biofilm (sediment) was enhanced by 99.3%. However, further increase in concentration of endogenous mediator proved to be limiting on reactor performance. Pyrosequencing and phylogenetic analysis on the basis of partial 16S rRNA sequences demonstrated both culturable and unculturable bacterial species in anodic biofilm and relative abundance of family Pseudomonadaceae was found to be maximum, i.e., 61.7% followed by Rhodocyclaceae 19.2%, Xanthomonadaceae 6.3% and Opitutaceae 3.18%.