Arbuscular mycorrhiza confers lead tolerance and uptake in Miscanthus sacchariflorus

The effects of an arbuscular mycorrhizal fungi (AMF) association on the growth, survival capabilities, nutrients and lead (Pb) uptake of Miscanthus sacchariflorus under different Pb concentrations were studied in the form of pot cultures. The treatments comprised inoculation or non-inoculation of the AMF, Gigaspora margarita, and the addition of three Pb concentrations to the soil (0, 100 and 1000?mg?kg^?1). The addition of Pb significantly decreased mycorrhizal colonisation. The inoculation of AMF with Pb increased chlorophyll content, Fv/Fm, total dry mass, indole-3-acetic acid (IAA), total nitrogen, and total phosphorus, whereas H₂O₂ level, indole-3-acetic acid oxidase (IAAO) activity, and peroxidase (POD) activity were low compared to those in the non-inoculated treatments. Moreover, the application of AMF together with Pb doses induces concentrations of Pb in the plant, where the higher dose of Pb (1000?mg?kg^?1) induces a lower content of Pb in the aerial part of the plant but a higher content in the root. G. margarita enhanced the tolerance of M. sacchariflorus against Pb toxicity, and facilitated the accumulation of Pb in the plant roots, whereas translocation to the shoots was inhibited at the highest dose Pb (1000?mg?kg^?1). However, in contaminated soil, the Pb removal capability of M. sacchariflorus with AMF was remarkable.     

Adsorption of phosphate ions from water using a novel cellulose-based adsorbent

A novel cellulose-based adsorbent, iron(III)-coordinated amino-functionalised poly(glycidylmethacrylate)-grafted cellulose [Fe(III)–AM-PGMACell] was developed for the removal of phosphate from water and wastewater. The scanning electron micrograph showed that AM-PGMACell has a rougher surface than cellulose and the adsorption of Fe(III) on AM-PGMACell made the surface even rougher. Infrared spectroscopy revealed that amino groups on the surface of AM-PGMACell complexed with Fe(III) played an important role in the removal of phosphate from solutions. X-Ray diffraction patterns showed a decrease in crystallinity after graft copolymerisation onto cellulose. The effects of contact time, initial sorbate concentration, pH, agitation speed, dose of adsorbent and temperature on the removal process were investigated. Maximum removal of 99.1% was observed for an initial concentration of 25 mg·L ^?1 at pH 6.0 and an adsorbent dose of 2.0 g·L ^?1. A two-step pseudo-first-order kinetic model and Sips isotherm model represented the measured data very well. Complete removal of 11.6 mg·L ^?1 phosphate from fertiliser industry wastewater was achieved by 1.6 g·L ^?1 Fe(III)–AM-PGMACell. The adsorbent exhibited very high reusability for several cycles. Overall, the study demonstrated that Fe(III)–AM-PGMACell can be used as an efficient adsorbent for the removal and recovery of phosphate from water and wastewater.     

Photoelectrochemical treatment of ammonium using seawater as a natural supporting electrolyte

In the present study, a photoelectrochemical process containing seawater as a natural low-cost supporting electrolyte was used to remove ammonium from wastewater in a continuous flow mode. Based on central composite design (CCD), response surface methodology (RSM) was employed to evaluate the performance of the process in ammonia removal. The effect of four main independent parameters, including initial ammonium concentration, hydraulic retention time (HRT), current intensity and initial pH on the removal of ammonia was evaluated by the model. The optimal initial ammonium concentration, HRT, current intensity and initial pH were 917 mg NH ₄? N;·L ^?1, 108 min, 1.8 A and 8.4, respectively. The high coefficients (R ²=0.97 and adjusted R ²=0.94) obtained by the analysis of variance (ANOVA) demonstrated close correlation between predicted and experimental values. Also, treating the reject water from the sludge dewatering unit as an ammonium-rich wastewater showed the effectiveness of the process for treating real wastewaters (86% ammonium removal). The results revealed that the present process can be an efficient method for ammonium removal from polluted effluents in coastal areas based on the availability of seawater as a cost-efficient supporting electrolyte.     

Pomegranate husk as an adsorbent in the removal of toxic chromium from wastewater

The use of a new sorbent developed from the husk of pomegranate, a famous fruit in Egypt, for the removal of toxic chromium from aqueous solution has been investigated. The batch experiment was conducted to determine the adsorption capacity of the pomegranate husk. The effects of initial metal concentration (25 and 50 mg l^?1), pH, contact time, and sorbent concentration (2–6 g l^?1) have been studied at room temperature. A strong dependence of the adsorption capacity on pH was observed, the capacity increased as the pH decreased, and the optimum pH value was pH 1.0. Adsorption equilibrium and kinetics were studied with different sorbent and metal concentrations. The adsorption process was fast, and equilibrium was reached within 3 h. The maximum removal was 100% for 25 mg l^?1 of Cr⁶⁺ concentration on 5 g l^?1 pomegranate husk concentration, and the maximum adsorption capacity was 10.59 mg g^?1. The kinetic data were analysed using various kinetic models—pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion equations—and the equilibrium data were tested using several isotherm models, Langmuir, Freundlich, Tempkin, Dubinin–Radushkevich, and Generalized isotherm equations. The Elovich and pseudo-second-order equations provided the greatest accuracy for the kinetic data, while Langmuir and Generalized isotherm models were the closest fit for the equilibrium data. The activation energy of sorption has also been evaluated as 0.236 and 0.707 kJ mol^?1 for 25 and 50 mg l^?1 chromium concentration, respectively.     

Quantitative analysis and sorption of cadmium in environmental samples with a functionalized synthetic polymer

Quantitative analysis of cadmium in environmental samples was achieved with a polymeric sorbent synthesized by copolymerization of N,N-dimethylacrylamide and allyl glycidyl ether/iminodiacetic acid as chelating monomers with N,N′-methylenebisacrylamide as cross-linker. The polymer was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, and scanning electron microscopy. The sorption capacity of the functionalized sorbent was 70 mg g^?1. The equilibrium sorption data of Cd(II) on polymeric sorbent were analyzed using Langmuir, Freundlich, Temkin, and Redlich–Peterson models. Based on equilibrium adsorption data, the constants at pH 4.2 and 20 °C were determined for the first three as 0.33 (L mg^?1), 17.5 (mg g^?1) (L mg^?1)^1/n, and 12.9 (J mol^?1). Recovery of 94% of the metal ion was obtained with 0.5 mol L^?1 nitric acid as an eluting agent.     

Heavy metals in the polychaete Glycera longipinnis from the southwest of India

Metal concentrations in sediment and in whole tissue of the benthic polychaete Glycera longipinnis collected along the southwest coast of India were analysed. Relative seasonal accumulation of metals (Cu, Pb, Cr, Ni, Zn, Cd, Hg) was studied by categorising the habitat as less polluted or highly polluted based on metal contamination routed through industrial and urban sources. The metal content in tissues varied seasonally in the ranges, Cu: 2.21–27.08 μg·g^?1, Pb: 0.06–4.92 μg·g^?1, Cr: 1.73–29.20 μg·g^?1, Ni: 1.60–4.61 μg·g^?1, Zn: 14.72–82.30 μg·g^?1, Cd: 0.04–1.38 μg·g^?1and Hg: below decetable limits to 0.86 μg·g^?1. Concentration of heavy metals was found to be high in the whole body of G. longipinnis pooled from the polluted transects. The results of this study suggest that G. longipinnis may act as a useful biological indicator for heavy metal pollution along the southwest coast of India.     

Electro-remediation of tailings from a multi-metal sulphide mine: comparing removal efficiencies of Pb,Zn, Cu and Cd

Sulphidic mine tailings characterised by high concentrations of heavy metals (Pb 3532?±?97?mg/kg, Zn 8450?±?154?mg/kg, Cu 239?±?18?mg/kg and Cd 14.1?±?0.3?mg/kg) and abundant carbonate (17%) were subjected to eight lab-scale electrodialytic remediation (EDR) experiments to investigate the influence of current density, treatment time and particle size on removal efficiency. Pb and Cu removal improved when increasing current density, while Zn and Cd removal did not. In contrast Zn and Cd removal improved by grinding the tailings, while Pb and Cu removal did not. At the highest current density (1.2?mA/cm²), 94%, 75%, 71% and 67% removal of Pb, Zn, Cu and Cd could be achieved, respectively, on grinded tailings in 28 days. Sequential chemical extraction made before and after EDR revealed larger oxidisable fractions of Zn, Cu and Cd, representing large fractions of sulphides, which was likely to be the main barrier to be removed as efficiently as Pb. This was in accordance with acid/base extraction tests in which Pb showed high solubility at both high and low pH (up to 65% and 86% of extraction, respectively), while considerable extraction of Zn (55%) happened only at low pH; and very limited extraction (<20%) of Cu and Cd occurred at any pH.     

Heavy metals uptake from aqueous solutions using marine algae (Colpomenia sinuosa): kinetics and isotherms

The adsorption of copper, zinc, cobalt, lead and cadmium ions onto Colpomenia sinuosa was studied as a function of contact time, initial metal ion concentration and initial pH. In addition, desorption studies were performed. Characterisation of this adsorbent was also confirmed by Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) analysis. Batch adsorption experimental data were analysed using Langmuir, Freundlich and Dubinin–Raduschkevich (D–R) adsorption isotherms. The results indicated that the biosorption equilibrium was well described by both the Freudlich and D–R isotherms. Moreover, sorption kinetics was performed and it was observed that equilibrium was reached in<60 min, which could be described by the pseudo-second-order kinetic model for all heavy metals. The sorption of heavy metals onto the biomass was largely dependent on the initial solution pH. The elution efficiency for heavy metal ions desorption from C. sinuosa was determined for 0.1 M HCl, 1.0 M HCl and 1.0 M HNO₃. Desorption efficiency and also adsorption capacity were highest for Pb(II). The results indicate that C. sinuosa has great potential for the removal of heavy metals in an ecofriendly process.     

Suitability of various chemically prepared activated carbons for the removal of copper(II) ions

Studies on the suitability of various chemically prepared activated carbons (CPACs) like straw carbon (SC), sawdust carbon (SDC), dates nut carbon (DNC) and commercial activated carbon (CAC) for the removal of copper(II) ions by adsorption from simulated wastewater have been carried out under batch mode at 30?±?1°C and the results are compared. The percentage removal of Cu(II) ions increased with a decrease in initial concentration, particle size and added electrolytes (ionic strength) and increased with an increase in contact time, dose of adsorbent and initial pH of the solution. The adsorption data were fitted with the Langmuir isotherm. The applicability of the first order kinetic equation viz. Lagergren equation was tested by correlation analysis. The adsorption process is concluded to be a spontaneous, first order reaction, occurring with increased randomness at the solid–liquid interface. Studies on the desorption of Cu²⁺-loaded activated carbons (ACs) were carried out with nitric acid (0.2–1?N). The possibility of reuse of the regenerated ACs in cycle (in cue-one after another) was tested. SC was found to be a suitable adsorbent alternative to CAC among CPACs for the removal of metal ions, in general, and Cu²⁺ ions, in particular.     

Purification of contaminated paddy fields by clean water irrigation over two decades

Paddy fields near a mining site in north part of Guangdong Province, PR China, were severely contaminated by heavy metals as a result of wastewater irrigation from the tailing pond. The following clean water irrigation for 2 decades produced marked rinsing effect, especially on Pb and Zn. Paddy fields continuously irrigated with wastewater ever since mining started (50 years) had 1,050.0 mg kg^?1 of Pb and 810.3 mg kg^?1 of Zn for upper 20 cm soil, in comparison with 215.9 mg kg^?1 of Pb and 525.4 mg kg^?1 of Zn, respectively, with clean water irrigation for 20 years. Rinsing effect mainly occurred to a depth of upper 40 cm, of which the soil contained highest metals. Copper and Cd in the farmlands were also reduced due to clean water irrigation. Higher availability of Pb might partly account for more Pb transferred from the tailing pond to the farmland and also more Pb removal from the farmland as a result of clean water irrigation. Neither rice in the paddy field nor dense weeds in the uncultivated field largely took up the metals. However, they might contribute to activate metals differently, leading to a different purification extent. Rotation of rice and weed reduced metal retention in the farmland soil, in comparison with sole rice growth. Harvesting of rice grain (and partially rice stalk) only contributed small fraction of total amount of removed metal. In summary, heavy metal in paddy field resulted from irrigation of mining wastewater could be largely removed by clean water irrigation for sufficient time.     

Ackee apple (Blighia sapida) seeds: a novel adsorbent for the removal of Congo Red dye from aqueous solutions

The ability of ackee apple (AA) seeds to remove Congo Red (CR) dye from aqueous solution was investigated. AA was characterised using thermo gravimetric analyser, scanning electron microscopy, Braunauer Emmett Teller, pH_pzc, elemental analysis and Boehm titration. The effects of operational parameters such as adsorbent dosage, contact time, initial dye concentration and solution pH were studied in a batch system. pH has a profound influence on the adsorption process. Maximum dye adsorption was observed at pH 3.0. The reaction was fast, reaching equilibrium in 90 min. Adsorption data were best described by Langmuir isotherm and the pseudo-second-order kinetic model with a maximum monolayer coverage of 161.89 mg·g^?1. Both boundary layer and intraparticle diffusion mechanisms were found to govern the adsorption process. Thermodynamic parameters such as standard free energy change (Δ G ⁰), standard enthalpy change (Δ H ⁰), and standard entropy change (Δ S ⁰) were studied. Values of Δ G ⁰ varied between?30.94 and?36.56 kJ·mol^?1, Δ H ⁰ was 25.61 kJ·mol^?1, and Δ S ⁰ was 74.84 kJ·mol^?1·K^?1, indicating that the removal of CR from aqueous solution by AA was spontaneous and endothermic in nature. Regeneration and reusability studies were carried out using different eluents. AA gave the highest adsorption efficiency up to four cycles when treated with 0.3 M HCl. AA was found to be an effective adsorbent for the removal of CR dye from aqueous solution.     

Stabilization of metals in acidic mine spoil with amendments and red fescue (<Emphasis Type="Italic">Festuca rubra</Emphasis> L.) growth

Stabilization of metals with amendments and red fescue (Festuca rubra, cv. Keszthelyi 2) growth was studied on an acidic and phytotoxic mine spoil (pH_KCl 3.20–3.26; Cd 7.1 mg kg^?1, Cu 120 mg kg^?1, Pb 2154 mg kg^?1 and Zn 605 mg kg^?1) from Gyöngyösoroszi, Hungary in a pot experiment. Raising the pH above 5.0 by lime (CaCO₃), and supplementing with 40 mg kg^?1nitrogen (NH₄NO₃) made this material suitable for plant growth. All cultures were limed with 0.5% (m/m) CaCO₃ (treatment 1), which was combined with 5% (m/m) municipal sewage sludge compost (treatment 2), 5% (m/m) peat (treatment 3), 7.5% (m/m) natural zeolite (clinoptilolite) (treatment 4), and 0.5 (m/m) KH₂PO₄ (treatment 5). Treatments 1–5 were combined with each other (treatment 6). After 60 days of red fescue growth, pH of the limed mine spoil decreased in all cultures units. Application of peat caused the highest pH decrease (1.15), while decrease of pH was less than 0.23 in treatments 2, 5 or 6. Application of lime significantly reduced concentrations of metals in the ‘plant available’ fraction of mine spoil compared to non-limed mine spoil. Amendments added to limed mine spoil changed variously the ratio of Cd, Cu, Pb and Zn in exchangeable or ‘plant available’ fractions, differently influencing the phytoavailability of these metals. Most of the metals were captured in the roots of test plants. Treatment 2 caused the appearance of less Cd in shoots (<0.1 μg g^?1) or roots (3.11 μg g^?1), while treatment 5 resulted in the highest Cd concentration (2.13 μg g^?1) in shoots. Treatments did not influence significantly the Cu accumulation in shoots. The Pb accumulation of roots (44.7 μg g^?1) was most effectively inhibited by combined treatment, while the highest value (136 μg g^?1) was found in the culture treated with potassium phosphate. Pb concentration in shoots was below the detection limit, except for treatments 5 and 6. Peat application resulted in higher Zn concentration (448 μg g^?1) in shoots than other amendments, where these values were around 100 μg g^?1. All amendments influenced positively the dry matter yield of red fescue grown in limed mine spoil, however the application of 0.5 phosphate was less favourable. Liming, application of amendments and growth of red fescue can stabilize metals in acidic and phytotoxic mine spoil, and by phytostabilization they can reduce the risk of metal contamination of the food chain.     

Multivariate optimization of Cd(II) biosorption onto Ulmus tree leaves from aqueous waste

Ulmus tree leaves were successfully used as a novel and efficient biosorbent for removing cadmium, (Cd(II)), from aqueous solutions in a batch system. A multivariate strategy for optimization of removal efficiency conditions of Cd(II) was carried out. A 2³ full factorial design with three center points (9 runs) was performed for screening the main variables and reducing the large number of experimental runs. Initial concentration of metal ion (C _m), amount of sorbent (m), and pH were considered as the three main variables at two different levels. The maximum removal efficiency of Cd(II) was achieved within 1 h contact time. It was found that all the main factors and their interactions were significant at p < 0.05. Doehlert response surface methodology was utilized (13 runs) for finding a suitable mathematical model. The analysis of variance and some statistical tests such as lack-of-fit, coefficient of determination (R ²), and residual distribution plot confirmed the validity of the model. The optimum conditions for maximum removal of Cd(II) by Ulmus tree leaves were found as pH = 3.4, m (amount of sorbent) = 0.128 g, C _m (initial concentration of metal ion) = 12.1 mg L^?1.     

Sonocatalytic degradation of tetracycline antibiotic in aqueous solution by sonocatalysis

Tetracycline (TC), one of the most common antibiotics, is often poorly bio-degraded in conventional wastewater treatment plants. In this study, the sonocatalytic degradation of TC was investigated using TiO₂ nano-particles as catalyst. The effect of pH, initial TC concentrations, reaction times, and H₂O₂ concentrations were evaluated. The efficacy of ultrasonic irradiation alone in the removal of this pollutant was negligible but removal efficiency increased upon addition of TiO₂ up to 250 mg L^?1; increase of pH and initial TC concentration attenuated TC degradation. Addition of H₂O₂ raised the removal efficiency so that complete removal of TC was achieved within 75 min.     

Lead(II) and cadmium(II) removal from aqueous solution using processed walnut shell: kinetic and equilibrium study

The biosorption potential of processed walnut shell for Pb(II) and Cd(II) ions from aqueous solutions was explored. The effects of pH, contact time, initial ion concentration, and amount of dried adsorbent were studied in batch experiments. The maximum adsorption was achieved within the pH range 4.0–6.0. The equilibrium data were well fitted by the Langmuir isotherm model. The maximum monolayer adsorption capacities were found to be 32?g?kg^?1 and 11.6?g?kg^?1 for Pb(II) and Cd(II) ions, respectively. Kinetic data were best described by the pseudo-second-order model. The structural features of the adsorbent were characterized by Fourier transform infrared spectroscopy, which confirmed the involvement of hydroxyl (–OH), carboxyl (–COO^–), and carbonyl (C=O) groups in metal sorption. This readily available adsorbent is efficient in the uptake of Pb(II) and Cd(II) ions from an aqueous solution and could be used for the treatment of wastewater streams bearing these metal ions.     

Response of roselle (Hibiscus sabdariffa) to heavy metals contamination in soils with different organic fertilisations

The response of green roselle (Hibiscus sabdariffa) to Cu/Pb contamination and manure application in soil was investigated using pot experiments. Subsamples of a mineral soil were treated with increasing doses (0–500 mg kg^?1) of Cu/Pb only and/or amended (at 10% w/w) with poultry or swine manure. Roselle plants were grown, monitored for changes in growth rate and post-harvest aboveground dry biomass and tissue Cu/Pb concentrations were determined. The plants were typically greenish with linear growth profiles at all metal doses, indicating some level of tolerance. Dry biomass yields decreased as metal dose increased. Poultry manure enhanced roselle biomass yields better than swine manure. Tissue Cu/Pb concentrations increased linearly as metal doses increased in unamended soils; whereas nonlinear responses were observed in manure-amended soils. Soil-to-plant transfer factors, T _f (%) indicated that Cu (13≤T _f (% )≤60) was more phytoavailable to roselle than Pb (11≤T _f (% )≤20). Tissue metal concentrations were modelled from soil pH, organic matter, plant available and pseudototal metal; but the models appeared more reliable with plant available metal as a covariate than with pseudototal metal content. These observations may become useful whenever phytoextraction is the remedial option for soils moderately contaminated by toxic metals.     

Metal levels in computer monitor components discarded in the vicinities of electronic workshops

Levels of Pb, Ni, Cr, Cu, Zn, and Cd in the glass screens (GS) and printed wiring boards (PWBs) of obsolete computer monitors (OCMs) were determined by flame atomic absorption spectrophotometry (FAAS) following standard digestion. Metal concentrations (mg kg^?1) in GS were in the following ranges (medians in brackets): Pb ND – 3100 (46), Cd 0.5–2.6 (0.8), Cr ND – 18.7 (3.1), and Zn 8.1–600 (37) and in PWBs (mg kg^?1): Pb 34,600 ± 17,000, Cd 11 ± 9, Cr 59 ± 45, Zn 15,900 ± 7800, Cu79,000 ± 22,600, and Ni 3200 ± 2500. In GS, the levels of the six metals were lower than their total threshold limit concentrations (TTLC), except for Pb with a TTLC of 1000 mg kg^?1 in 10% of the samples. In the PWBs, the TTLC of Pb and Cu (2500 mg kg^?1) was exceeded many fold. For Zn (5000 mg kg^?1) and Ni (2000 mg kg^?1); they were exceeded by 90% and 65%, respectively. For OCMs manufactured in 2001 and later, Pb and Zn levels in GS and Cr, Zn, and Ni in PWBs were significantly reduced.     

Cadmium accumulation by green algae Cladophora glomerata (L.) Kutz. (Chlorophyta) in presence of Nile tilapia Oreochromis niloticus (L.)

Accumulation of metals by aquatic organisms is mostly affected by other biological components in environments. In this study, cadmium (Cd) accumulation in green algae, Cladophora glomerata (L.) Kutz., exposed to 0.1 and 1.0 mg L^?1 of Cd for 15 and 30 days was examined in laboratory conditions in the presence of Nile tilapia Oreochromis niloticus (L.). The green algae C. glomerata accumulated Cd concentrations as 690 ± 70 and 3430 ± 470 mg kg^?1 on day 15, and 1130 ± 180 and 6830 ± 1540 mg kg^?1 on day 30. There were significant increases (p < 0.05) in metal accumulation by green algae as the exposure time and metal concentration increased. The results also indicated that the presence of Nile tilapia in the medium led to a significant Cd accumulation in the green algae compared to control (p < 0.05).     

Toxicity and bioaccumulation of heavy metals in mullet fish Liza klunzingeri (Mugilidae: Perciformes)

The mullet fish, Liza klunzingeri, commercially important and widely relished by Kuwaiti residents, and the stressed ecosystem in Kuwait Bay instigated us to conduct toxicity and bioaccumulation tests on heavy metals (Pb, Ni, V, Cu and Fe). Among five metals, Pb had the lowest observed effect concentration (LOEC) at 1 μg?l ^?1. Using multi-factor Probit analysis, toxicity tests (72 h) on L. klunzingeri reared in filtered sea water in the laboratory showed Pb with maximum effect at median lethal concentration (LC₅₀) followed by V, Ni, Cu and Fe. Their bioaccumulation factor (BAF) was in the sequence Pb>V>Fe>Cu and Ni. For fish exposed for 30 d, bioaccumulation exhibited increasing metal levels in liver followed by gills and muscles. These results suggest the potential use of L. klunzingeri as a bioindicator of metal pollution in the future.