Phytoremediation of phenol using Polygonum orientale,including optimized conditions

Removing phenol from wastewater has become a major challenge of international concern. Phytoremediation is a novel and eco-friendly method and is attracting an increasing amount of attention for treating phenol in wastewater. We studied the ability of Polygonum orientale, which is frequently present around water bodies and in wetlands in China, to phytoremediate phenol. We determined the inhibition concentration for phenol on P. orientale using emergency toxicology experiments and morphological observations. Isothermal and kinetic models were created to assess the adsorption process involved in phenol removal. Comparison tests in sterile conditions demonstrated that metabolic removal was the main way in which the phenol concentrations were decreased, and removal by adsorption played a smaller role. An orthogonal test was performed to determine the optimum conditions under which P. orientale will remove phenol, and these were found to be an initial phenol concentration of 5 mg L^?1, 100 % natural light, and a 13-day treatment time. These results provide a theoretical basis for increasing our understanding of the mechanisms involved in the removal of phenol by P. orientale and will help in developing its application in the greening of urban areas to provide both phytoremediation and esthetic landscaping.     

Adsorption of ammonium from simulated wastewater by montmorillonite nanoclay and natural vermiculite: experimental study and simulation

In this research, montmorillonite nanoclay (MNC) and vermiculite were used to adsorb ammonium (NH₄ ⁺) from simulated wastewater. The effect of organic acids, cations, and anions on adsorption of NH₄ ⁺ was also studied using batch experiments. The presence of organic acids significantly decreased the NH₄ ⁺ adsorption using both adsorbents and the reduction followed the order of citric acid > malic acid > oxalic acid. The presence of cations in wastewater could decrease the adsorption of NH₄ ⁺ and the ion exchange selectivity on the MNC and vermiculite followed the orders Mg > Ca ≥ K > Na and Mg > > Ca > Na > K, respectively. Adsorption of NH₄ ⁺ by adsorbents in the presence of sulfate (SO₄) was higher than those in the presence of phosphate (PO₄) and chloride (Cl) anions. Results indicated that MNC and vermiculite had good potential for NH₄ ⁺ removal depending on adsorbent dosage, pH, contact time, and initial NH₄ ⁺ concentration. The effect of pH on removal of NH₄ ⁺ indicated that MNC would be more appropriate as the adsorbent than vermiculite at low pH values. Kinetic analysis demonstrated that the rate-controlling step adsorption for NH₄ ⁺ by MNC and vermiculite was heterogeneous chemisorption and followed the pseudo-second-order model. The desorption experiments indicated that the adsorption of NH₄ ⁺ by adsorbents was not fully reversible, and the total recovery of adsorbed NH₄ ⁺ for MNC and vermiculite varied in the range of 72 to 94.6% and 11.5 to 45.7%, respectively. Cation exchange model (CEM) in PHREEQC program was used to simulate NH₄ ⁺ adsorption. Agreement between measured and simulated data suggested that CEM was favored in simulating adsorption of NH₄ ⁺ by clay minerals. The results indicated that MNC and vermiculite have good performance as economic and nature-friendly adsorbents that can ameliorate the water and environment quality.     

Assessment of phenol infiltration resilience in soil media by HYDRUS-1D transport model for a waste discharge site

The movement of contaminants through soil imparts a variety of geo-environmental problem inclusive of lithospheric pollution. Near-surface aquifers are often vulnerable to contamination from surface source if overlying soil possesses poor resilience or contaminant attenuation capacity. The prediction of contaminant transport through soil is urged to protect groundwater from sources of pollutants. Using field simulation through column experiments and mathematical modeling like HYDRUS-1D, assessment of soil resilience and movement of contaminants through the subsurface to reach aquifers can be predicted. An outfall site of effluents of a coke oven plant comprising of alarming concentration of phenol (4–12.2 mg/L) have been considered for studying groundwater condition and quality, in situ soil characterization, and effluent characterization. Hydrogeological feature suggests the presence of near-surface aquifers at the effluent discharge site. Analysis of groundwater of nearby locality reveals the phenol concentration (0.11–0.75 mg/L) exceeded the prescribed limit of WHO specification (0.002 mg/L). The in situ soil, used in column experiment, possess higher saturated hydraulic conductivity (K _S ?=?5.25?×?10^?4 cm/s). The soil containing 47 % silt, 11 % clay, and 1.54 % organic carbon content was found to be a poor absorber of phenol (24 mg/kg). The linear phenol adsorption isotherm model showed the best fit (R ²?=?0.977, RMSE?=?1.057) to the test results. Column experiments revealed that the phenol removal percent and the length of the mass transfer zone increased with increasing bed heights. The overall phenol adsorption efficiency was found to be 42–49 %. Breakthrough curves (BTCs) predicted by HYDRUS-1D model appears to be close fitting with the BTCs derived from the column experiments. The phenol BTC predicted by the HYDRUS-1D model for 1.2 m depth subsurface soil, i.e., up to the depth of groundwater in the study area, showed that the exhaustion point was reached within 12 days of elapsed time. This clearly demonstrated poor attenuation capacity of the soil to retard migration of phenol to the groundwater from the surface outfall site. Suitable liner, based on these data, may be designed to inhibit subsurface transport of phenol and thereby to protect precious groundwater from contamination.     

Biosorption properties of Morus alba L. for Cd (II) ions removal from aqueous solutions

The abundantly available industrial waste product Morus alba L. pomace (MAP) is one of the cost-effective biosorbent for removal of metal ions from aqueous solutions. Hence, in the present study, we aimed to test the ability of MAP to remove Cd(II) ions through batch biosorption process. Firstly, MAP was characterized using several techniques, and then the influence of various experimental parameters such as initial pH of the aqueous solution, initial Cd(II) concentration, contact time, MAP concentration, and temperature were evaluated upon the biosorption process. It was found that the maximum uptake of Cd(II) ions occurred at initial pH 6.0 and optimum contact time was observed as 60 min. Cd(II) ions adsorption on MAP analyzed by the Langmuir and Freundlich isotherm models and the maximum monolayer biosorption capacity of MAP was found to be 21.69 mg?g^?1 by using the Langmuir isotherm model. The pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion models were employed to describe the biosorption kinetics. In order to investigate the thermodynamic properties of the biosorption process, the changes in the Gibbs free energy (?G), enthalpy (?H), and entropy (?S) were also evaluated and it has been concluded that the process was feasible, spontaneous, and endothermic in the temperature range of 5–40 °C.     

Some soil properties on coal mine spoils reclaimed with black locust (Robinia pceudoacacia L.) and umbrella pine (Pinus pinea L.) in Agacli-Istanbul

This study performed on randomly selected seven sample plots in leguminous black locust (Robinia pceudoacacia L.) plantations and five sample plots in umbrella pine (Pinus pinea L.) plantations on coal mine soil/spoils. Soil samples were taken from eight different soil depths (0–1, 1–3, 3–5, 5–10, 10–20, 20–30, 30–40, and 40–50 cm) into the soil profile. On soil samples, bulk density, fine soil fraction (Ø < 2 mm), sand, silt and clay rates, soil acidity (pH), organic carbon (C_org), and total nitrogen (N_t) contents were investigated. Also, some forest floor properties (unit mass, organic matter, and total nitrogen) were determined, and results were compared statistically between umbrella pine and black locust. As a result, 17 years after plantations, total forest floor accumulation determined as 6,107 kg ha^???1 under black locust compared to 13,700 kg ha^???1 under umbrella pine. The more rapid transformation of leguminous black locust forest floor creates organic carbon that migrates further into the mineral profile, and rapid accumulation of C and N in the soil profile was registered. Slower transformation processes of forest floor under umbrella pine result in lower soil N ratio and greater quantity of forest floor. Higher soil pH under leguminous black locust was determined significantly than umbrella pine. In conclusion, the composition of symbiotic nitrogen fixation of black locust appears to be a possible factor favoring carbon and nitrogen accumulation and, consequently, soil development. Clearly, both tree species have favorable impacts on initial soil formation. The umbrella pine generates the more forest floor layer; in contrast, black locust forest floor incorporates into the soil more rapidly and significantly increases soil nitrogen in upper soil layers.     

Fruit Stones from Industrial Waste for the Removal of Lead Ions from Polluted Water

Lead, one of the earliest metals recognized and used by humans, has a long history of beneficial use. However, it is now recognized as toxic and as posing a widespread threat to humans and wildlife. Treatment of lead from polluted water and wastewater has received a great deal of attention. Adsorption is one of the most common technologies for the treatment of lead-polluted water. This technique was evaluated here, with the goal of identifying innovative, low-cost adsorbent. This study presents experiments undertaken to determine the suitable conditions for the use of peach and apricot stones, produced from food industries as solid waste, as adsorbents for the removal of lead from aqueous solution. Chemical stability of adsorbents, effect of pH, adsorbents dose, adsorption time and equilibrium concentration were studied. The results reveal that adsorption of lead ions onto peach stone was stronger than onto apricot stone up to 3.36% at 3 h adsorption time. Suitable equilibrium time for the adsorption was 3–5 h (% Pb adsorption 93% for apricot and 97.64% for peach). The effective adsorption range for pH in the range was 7–8. Application of Langmuir and Freundlich isotherm models show high adsorption maximum and binding energies for using these adsorbents for the removal of lead ions from contaminated water and wastewater.     

Removal of mercury(II) ions in aqueous solution using the peel biomass of <Emphasis Type="Italic">Pachira aquatica</Emphasis> Aubl: kinetics and adsorption equilibrium studies

Mercury is a highly toxic substance that is a health hazard to humans. This study aims to investigate powders obtained from the peel of the fruit of Pachira aquatica Aubl, in its in natura and/or acidified form, as an adsorbent for the removal of mercury ions in aqueous solution. The materials were characterized by Fourier transform infrared spectroscopy and thermogravimetric analysis. The infrared spectra showed bands corresponding to the axial deformation of carbonyls from carboxylic acids, the most important functional group responsible for fixing the metal species to the adsorbent material. The thermograms displayed mass losses related to the decomposition of three major components, i.e., hemicellulose, cellulose, and lignin. The adsorption process was evaluated using cold-vapor atomic fluorescence spectrometry (CV AFS) and cold-vapor atomic absorption spectrometry (CV AAS). Three isotherm models were employed. The adsorption isotherm model, Langmuir-Freundlich, best represented the adsorption process, and the maximum adsorption capacity was predicted to be 0.71 and 0.58 mg g^?1 at 25 °C in nature and acidified, respectively. Adsorption efficiencies were further tested on real aqueous wastewater samples, and removal of Hg(II) was recorded as 69.6 % for biomass acidified and 76.3 % for biomass in nature. Results obtained from sorption experiments on real aqueous wastewater samples revealed that recovery of the target metal ions was very satisfactory. The pseudo-second-order model showed the best correlation to the experimental data. The current findings showed that the investigated materials are potential adsorbents for mercury(II) ion removal in aqueous solution, with acidified P. aquatica Aubl being the most efficient adsorbent.     

Rapid spectrophotometric determination of trace amounts of palladium in water samples after dispersive liquid–liquid microextraction

A simple, rapid, and efficient dispersive liquid–liquid microextraction method, followed by UV–Vis spectrophotometry was developed for the preconcentration and determination of Pd ions in water samples. Pd ions react with α-furildioxime (chelating agent) to form a hydrophobic complex. Various parameters were altered to study and optimize their effects on the extraction efficiency, such as pH, ligand concentration, the type and volume of extraction and dispersive solvents, extraction time, and salt concentration. Under optimized conditions, the method exhibited an enrichment factor (C _org/C _aq) of 25 and recovery more than 98 % within a very short extraction time. The linearity of the method ranged from 10 to 200 μg?L^?1. The limit of detection was 1.1 μg?L^?1. The relative standard deviation for the concentration of 100 μg?L^?1 of Pd was 2.3 % (n?=?10). Finally, the developed method was successfully applied to the extraction and determination of Pd in tap, river, mineral, and sea water samples.     

Planted floating bed performance in treatment of eutrophic river water

The objective of the study was to treat eutrophic river water using floating beds and to identify ideal plant species for design of floating beds. Four parallel pilot-scale units were established and vegetated with Canna indica (U1), Accords calamus (U2), Cyperus alternifolius (U3), and Vetiveria zizanioides (U4), respectively, to treat eutrophic river water. The floating bed was made of polyethylene foam, and plants were vegetated on it. Results suggest that the floating bed is a viable alternative for treating eutrophic river water, especially for inhibiting algae growth. When the influent chemical oxygen demand (COD) varied from 6.53 to 18.45 mg/L, total nitrogen (TN) from 6.82 to 12.25 mg/L, total phosphorus (TP) from 0.65 to 1.64 mg/L, and Chla from 6.22 to 66.46 g/m³, the removal of COD, TN, TP, and Chla was 15.3 %–38.4 %, 25.4 %–48.4 %, 16.1 %–42.1 %, and 29.9 %–88.1 %, respectively. Ranked by removal performance, U1 was best, followed by U2, U3, and U4. In the floating bed, more than 60 % TN and TP were removed by sedimentation; plant uptake was quantitatively of low importance with an average removal of 20.2 % of TN and 29.4 % of TP removed. The loss of TN (TP) was of the least importance. Compared with the other three, U1 exhibited better dissolved oxygen (DO) gradient distributions, higher DO levels, higher hydraulic efficiency, and a higher percentage of nutrient removal attributable to plant uptake; in addition, plant development and the volume of nutrient storage in the C. indica tissues outperformed the other three species. C. indica thus could be selected when designing floating beds for the Three Gorges Reservoir region of P. R. China.     

Mineral contents of seed and seed oils of Capparis species growing wild in Turkey

The mineral contents of seed and seed oils of Capparis species growing wild in Turkey were established by inductively coupled plasma–atomic emission spectrometry. Capparis spinosa var. spinosa (2010) and Capparis ovata var. canescens variety (2009) were determined to be rich in terms of mineral matter as 19,514.60 and 16,995.92 ppm as a total, respectively. C. spinosa var. spinosa collected from Mu?la-Milas region (2009) had the highest amount of Ca with 1,010.67 ppm in C. spinosa species and in C. ovata species. C. ovata var. canescens collected from Ankara-Beypazar? (2010) region had the highest amount of Ca with 833.92 ppm Ca amount in C. spinosa var. spinosa, inermis, herbaceae seeds decreased in 2010. C. spinosa var. inermis collected from Antalya-Serik (2010) in C. spinosa species had rich amount of Ca with 123.78 ppm and C. ovata var. palaestina seed oils collected from Mardin-Savur region (2009) had rich amount of Ca with 253.71 ppm in C. ovata species. The oil of C. spinosa var. herbaceae variety collected from Mardin-Midyat region (2010) was determined to have the highest major mineral matter (Ca, K, Mg, Na, and P) with 1,424.37 ppm in C. spinosa species. It was also determined that as a result, caper seed and oils were found to be important sources of nutrients and essential elements.     

Characterization of phytotoxicity of metal engraving effluent samples

Two effluent samples were collected from an acid bath of a metal engraving industry. Sample A was lime-treated to pH 6 and sample B, pH 9. Zn concentrations in samples A and B were 1207 and 4.24 mg L^-1, respectively. Both samples A and B caused 100% inhibition on millet seed germination. Sample A was more toxic than B. The 60% concentration of sample A caused 96% inhibition, whereas the 60% concentration of sample B caused 60% inhibition. The toxicity of sample B was not likely due to the presence of cyanide and zinc ions. The results of using various adsorbents and resins for the effluent treatment showed that only powdered activated carbon was partially effective in toxicity removal. By a combination of treatment methods, including using sodium hydroxide precipitation and carbon column adsorption, toxicity removal was calculated to be 29%.     

Factors affecting metribuzin retention in Algerian soils and assessment of the risks of contamination

Metribuzin is a widely used herbicide around the world but it could lead to soil and water contamination. Metribuzin retention on a silty–clay agricultural soil of Algeria was studied in laboratory batch experiments to assess the contamination risk of the groundwater. Factors conditioning the fate of metribuzin were investigated: soil nature, metribuzin formulation, NPK fertilizer, and soil pH. Freundlich sorption isotherms gave the coefficients K _F between 1.2 and 4.9 and 1/n _a between 0.52 and 0.93. The adsorption is directly dependent on organic and clay soil contents. Formulated metribuzin (Metriphar) reduces the adsorption (K _F?=?1.25) compared to pure metribuzin (K _F?=?2.81). The addition of an NPK fertilizer decreases the soil pH (6.67 for the soil without fertilizer and 5.86 for 2 % of fertilizer) and increases metribuzin adsorption (K _F is 4.83 for 2 % of fertilizer). The pH effect on the adsorption is corroborated in experiments changing the soil pH between 5 (K _F is 4.17) and 8 (K _F is 1.57) under controlled conditions. Desorption isotherms show a hysteresis and only 30 to 40 % of the initially adsorbed metribuzin is released. The estimated GUS index is ≥2.8 for a DT50?≥?30 days. K _F values and the hysteresis show that metribuzin is little but strongly retained on the soil. Formulated metribuzin and addition of fertilizer affect the retention. However, the GUS index indicates a high mobility and a significant risk of leaching. The most appropriate risk management measure would be an important increase in organic matter content of the soil by addition of organic amendments.     

Dissipation and residue of famoxadone in grape and soil

The analytical method of famoxadone residue and its dissipation in grape and soil were investigated. Famoxadone (68.75% water-dispersible granule) was applied at two dosages (1.25 and 2.5 g l^???1). Soil and grape samples were collected at intervals and analyzed for famoxadone residues. The results showed that the degradation rate of famoxadone in grape and soil were similar, and their dynamics could be described by C?=?1.1738e ^???0.0562t with correlation coefficient r?=?0.9044 in grape and C?=?5.6565e ^???0.0515t with r?=?0.9620 in soil, respectively. Half-lives were 12.3 and 13.5 days in grape and soil, respectively. The results indicated that at harvest time, the residues of famoxadone in grape were well below the EU’s maximum residue level (2 mg kg^???1) and was safe to apply in grape.     

Treatment of wastewater containing arsenic using Rhazya stricta as a new adsorbent

The effective removal of heavy metals from aqueous wastes is among the most important issues for many industrialized countries. Removal of arsenic (As) from aqueous solutions was studied using Rhazia stricta biomass. The batch experiments are carried out to investigate the effect of the significant process parameters such as pH, contact time, solute concentration and adsorbent dose. The optimum pH required for maximum adsorption was found to be 5. The equilibrium data for the adsorption of As(V) on R. stricta are tested with various adsorption isotherm models such as Langmuir, Freundlich, Tempkin and Generalized equation. Results indicate the following order to fit the isotherm: Langmuir (1 and 2)?>?Tempkin?>?Generalized form?>?Freundlich. A comparison of two kinetic models showed that our data fitted well to the Elovich model.     

Characterisation of coal washery effluent and optimisation of coagulation behaviour of <Emphasis Type="Italic">Moringa oleifera</Emphasis> seed as a coagulant

The huge quantity of effluent generated in coal washing processes contains large amount of suspended and dissolved solids, clay minerals, coal fines and other impurities associated with raw coal. The present system of recirculation of the effluent is found to be ineffective in removing colloidal fines, which is the major part of the impurities present in washery effluent. Hence, there is a need for the assessment of a better technique for an efficient removal of these impurities. This study deals with detailed characterisation of coal washery effluent and fine particles present in it. For efficient removal of impurities, the suitability of biocoag-flocculation process using Moringa oleifera seed biomass as a natural coagulant was examined. Various doses of M. oleifera ranging from 0.2 to 3 mL/L were used in order to determine the optimal conditions. The impact of the variations in pH of the effluent (2–10), contact time (5–30 min), settlement time (5–50 min), temperature (10–50 °C) and the effluent dilution (1:0–1:5) was also assessed to optimise the treatment process. Post treatment analysis was carried out for determination of the different parameters such as pH, conductivity, turbidity, solids and settling velocity. Excellent reduction in turbidity (97.42%) and suspended solids (97.78%) was observed at an optimum dose of M. oleifera seed coagulant of 0.8 mL/L with an optimum contact time of 15 and at 20 min of settling time. In comparison with very few past studies of M. oleifera in the treatment of coal washery effluent with high dose and inadequate removal, this study stands to be a major highlight with low dose and high removal of the impurities. M. oleifera coagulant is considered to be an environment-friendly material, therefore, its application is recommended for simple and efficient treatment of coal washery effluent.     

Dissipation pattern and pre-harvest residue limit of abamectin in perilla leaves

The pre-harvest residue limit (PHRL) of abamectin (abamectin B1a and B1b) in Perilla frutescens leaves grown under greenhouse conditions were investigated using high-performance liquid chromatography with a fluorescence detector. Samples were extracted with acetonitrile. The extract was purified through a solid phase extraction procedure. Then the purified extract was derivatized with trifluoroacetic anhydride and N-methylimidazole to form a strong stable fluorescent derivative of abamectin. Finally, derivatized abamectins were conveyed to the detector via an Atlantis C₁₈ column, with water and methanol as a mobile phase. Calibration curves were linear over the calibration ranges with coefficients of determinants r ²?≥?0.999. The limits of detection and quantification were 0.0033 and 0.01 mg kg^?1 for abamectin B_1a and B_1b, respectively. Recovery was assessed in a control matrix at two different fortification concentrations, with three replicates for each concentration. Good recoveries were obtained for the target analytes and ranged from 82.11 to 93.03 %, with relative standard deviations of less than 8 %. The rate of disappearance of total abamectin on perilla leaves for recommended and double the recommended doses was described as first-order kinetics with a half-life of 0.7 days. Using the PHRL curve, we could predict the residue level of total abamectin to be 0.92 mg kg^?1 at 7 days before harvest or 0.26 mg kg^?1 at 4 days before harvest, which would be below the provisional MRL designed by the Korea Food and Drug Administration.     

Arsenic and other trace elements in two catfish species from Paranaguá Estuarine Complex, Paraná, Brazil

Concentrations of arsenic and four additional trace elements (Cu, Cr, Ni, and Zn) were determined by inductively coupled plasma–optical emission spectrometry in the muscular tissue of the yellow catfish (Cathorops spixii) and the urutu catfish (Genidens genidens) from Paranaguá Estuarine Complex, Brazil (PEC). The PEC can be characterized by an environment of high ecological and economic importance in which preserved areas of rainforest and mangroves coexist with urban activities as ports and industries. The average concentrations (in milligram per kilogram dry weight) of elements in the muscle tissue of C. spixii are as follows: Zn (31), As (17), Cu (1.17), Cr (0.62), and Ni (0.28). Similar concentrations could be found in G. genidens with exception of As: Zn (36), As (4.78), Cu (1.14), Cr (0.51), and Ni (0.14). Fish from the geographic northern rural region (Guaraqueçaba–Benito) display higher As concentrations in the muscle tissues than fish found in the south-western (urban) part of the PEC. An international comparison of muscle tissue concentrations of trace elements in fish was made. Except for Ni in C. spixii, a tendency of decrease in element concentration with increasing size (age) of the fish could be observed. According to the National Health Surveillance Agency of Brazil, levels of Cr and As exceeded the permissible limits for seafood. An estimation of the provisional tolerable weekly intake of As was calculated with 109 % for C. spixii and with 29 % for G. genidens.     

Adsorption and detection of some phenolic compounds by rice husk ash of Kenyan origin

Rice husk ash (RHA) obtained from a rice mill in Kenya has been used as an inexpensive and effective adsorbent (and reagent) for the removal (and detection) of some phenolic compounds in water. The abundantly available rice mill waste was used in dual laboratory-scale batch experiments to evaluate its potential in: (i) the removal of phenol, 1,3-dihydroxybenzene (resorcinol) and 2-chlorophenol from water; and (ii) the detection of 1,2-dihydroxybenzene (pyrocatechol) and 1,2,3-trihydroxybenzene (pyrogallol) present in an aqueous medium. The studies were conducted using synthetic water with different initial concentrations of the phenolic compounds. The effects of different operating conditions (such as contact time, concentration of the phenolic compounds, adsorbent quantity, temperature, and pH) were assessed by evaluating the phenolic compound removal efficiency as well as the extent of their color formation reactions (where applicable). RHA exhibits reasonable adsorption capacity for the phenolic compounds and follows both Langmuir and Freundlich isotherm models. Adsorption capacities of 1.53 x 10(-4), 8.07 x 10(-5), and 1.63 x 10(-6) mol g(-1) were determined for phenol, resorcinol and 2-chlorophenol, respectively. Nearly 100% adsorption of the phenolic compounds was possible and this depended on the weight of RHA employed. For the detection experiments, pyrocatechol and pyrogallol present in water formed coloured complexes with RHA, with the rate of colour formation increasing with temperature, weight of RHA, concentration of the phenolic compounds and sonication. This study has proven that RHA is a useful agricultural waste product for the removal and detection of some phenolic compounds.     

Water chemistry influences the toxicity of silver to the green-lipped mussel Perna viridis

The study determined the influence and relative importance of water chemistry parameters (pH, alkalinity, hardness) on the acute toxicity of silver to the green mussel Perna viridis. A preliminary bioassay revealed that 4 mg L^???1 of silver caused 50% mortality (LC₅₀) in 96 h for mussels placed in seawater with pH 8.5, hardness 1,872 mg L^???1, and alkalinity 172 mg L^???1. Mortality of mussels increased with decreasing pH and increasing hardness and alkalinity variables. In contrast the mortality decreased with increasing pH and decreasing hardness and alkalinity values. The water chemistry also affected the concentration of sliver in experimental seawater and bioaccumulation of silver in mussels. The results revealed that the chemical properties of seawater must be considered while conducting toxicity tests with metals like silver. The possible explanations for the influence of water chemistry on silver toxicity to P. viridis are discussed.     

Almond shell activated carbon: adsorbent and catalytic support in the phenol degradation

In this work, two technologies are studied for the removal of phenol from aqueous solution: dynamic adsorption onto activated carbon and photocatalysis. Almond shell activated carbon (ASAC) was used as adsorbent and catalytic support in the phenol degradation process. The prepared catalyst by deposition of anatase TiO₂ on the surface of activated carbon was characterized by scanning electron microscopy, sorption of nitrogen, X-ray diffraction, Fourier transform infrared (FT-IR) spectroscopy, and pH_ZPC point of zero charge. In the continuous adsorption experiments, the effects of flow rate, bed height, and solution temperature on the breakthrough curves have been studied. The breakthrough curves were favorably described by the Yoon–Nelson model. The photocatalytic degradation of phenol has been investigated at room temperature using TiO₂-coated activated carbon as photocatalyst (TiO₂/ASAC). The degradation reaction was optimized with respect to the phenol concentration and catalyst amount. The kinetics of disappearance of the organic pollutant followed an apparent first-order rate. The findings demonstrated the applicability of ASAC for the adsorptive and catalytic treatment of phenol.