Dietary high protein and vitamin C mitigates endosulfan toxicity in the spotted murrel, Channa punctatus (Bloch, 1793)

The amelioration effect of dietary high protein and vitamin C against stress was evaluated in spotted murrel, Channa punctatus, exposed to endosulfan. Two hundred and forty fish (average weight: 27.01 g/fish), distributed equally into 4 different groups (control, T₁, T₂, and T₃), each with 6 replicates were fed with control (40% crude protein, CP and 0.1% vitamin C), T₁ (40% CP and 0.1% vitamin C), T₂ (50% CP and 0.1% vitamin C), and T₃ (50% CP and 0.2% vitamin C) diets for 90 days. Groups fed T₁, T₂, and T₃ diets were exposed to sublethal endosulfan concentration, whereas the control was maintained without endosulfan exposure. Results indicated significant reduction in the growth performance, survival, and activities of lactate dehydrogenase (liver and muscle), malate dehydrogenase (liver and muscle), enzymes of protein metabolism (aspartate amino transferase in liver and alanine amino transferase in liver and muscle), acetyl choline esterase (brain), alkaline phosphatase activity (liver), and ATPase (gill) enzymes of group fed control diet and exposed to endosulfan. However, endosulfan exposed fish fed high CP and vitamin C diet exhibited significant (P < 0.05) improvement in their growth performance and metabolic enzyme activities. Further, high CP and vitamin C diet reduced endosulfan accumulation in the muscle. Overall results indicate that vitamin C (0.2%) supplementation in high CP (50%) diet improves growth, metabolism, and reduce endosulfan bioaccumulation in C. punctatus.     

Influences of humic acid, bicarbonate and calcium on Cr(VI) reductive removal by zero-valent iron

The influences of various geochemical constituents, such as humic acid, HCO₃⁻, and Ca²⁺, on Cr(VI) removal by zero-valent iron (Fe⁰) were investigated in a batch setting. The collective impacts of humic acid, HCO₃⁻, and Ca²⁺ on the Cr(VI) reduction process by Fe⁰ appeared to significantly differ from their individual impacts. Humic acid introduced a marginal influence on Fe⁰ reactivity toward Cr(VI) reduction, whereas HCO₃⁻ greatly enhanced Cr(VI) removal by maintaining the solution pH near neutral. The Cr(VI) reduction rate constants (k_obs) were increased by 37.8% and 78.3%, respectively, with 2 mM and 6 mM HCO₃⁻ in solutions where humic acid and Ca²⁺ were absent. Singly present Ca²⁺ did not show a significant impact to Cr(VI) reduction. However, probably due to the formation of passivating CaCO₃, further addition of Ca²⁺ to HCO₃⁻ containing solutions resulted in a decrease of k_obs compared to solutions containing HCO₃⁻ alone. Ca²⁺ enhanced humic acid adsorption led to a minor decrease of Cr(VI) reduction rates. In Ca²⁺-free solutions, humic acid increased the amount of total dissolved iron to 25 mg/l due to the formation of soluble Fe-humate complexes and stably dispersed fine Fe (oxy)hydroxide colloids, which appeared to suppress iron precipitation. In contrast, the coexistence of humic acid and Ca²⁺ significantly promoted the aggregation of Fe (oxy)hydroxides, with which humic acid co-aggregated and co-precipitated. These aggregates would progressively be deposited on Fe⁰ surfaces and impose long-term impacts on the permeability of PRBs.     

Influence of biofilm on the transport of fullerene (C60) nanoparticles in porous media

The significance of biofilm on fullerene C₆₀ nanoparticles transport and deposition were examined both in porous media and quartz crystal microbalance with dissipation (QCM-D) systems under a variety of environmentally relevant ionic strength (1-25 mM in NaCl and 0.1-5 mM in CaCl₂) and flow conditions (4-8 m day⁻¹). The magnitudes of deposition rate coefficients (k_d) were compared between porous media with and without biofilm extracellular polymeric substances (EPS) coating under equivalent fluid velocities and solution chemistries. The observed k_d were greater in porous media with biofilm EPS coating relative to those without biofilm EPS coating across the entire solution ionic strengths and fluid velocities examined, demonstrating that the enhancement of C₆₀ deposition by the biofilm EPS coating is relevant to a wide range of environmental conditions. This greater deposition was also observed on silica surfaces with biofilm EPS coating in QCM-D system. The results clearly showed that biofilm EPS have a great influence on C₆₀ deposition. Derjaguin-Landau-Verwey-Overbeek (DLVO) theory could not explain the enhanced C₆₀ deposition by biofilm EPS. Biochemical and physical characteristics of biofilm EPS were responsible for the increased C₆₀ deposition.     

Fluctuating wing asymmetry and hepatic concentrations of persistent organic pollutants are associated in European shag (Phalacrocorax aristotelis) chicks

In aquatic birds, high body burdens of persistent organic pollutants (POPs) have been associated with developmental effects related to growth, increased fluctuating wing asymmetry, and disruption of the thyroid hormone, vitamin A (retinol) and vitamin E (tocopherol) homeostasis. The aim of the present study was to examine if morphological variables (body mass, liver mass, wing length, tarsus length and head length), fluctuating asymmetry of the wings and tarsus, growth rates and endocrine variables (thyroid hormones, retinol and tocopherol) were associated with hepatic levels of POPs (PCBs, OCPs and PBDEs) in 21 day old chicks of European shag (Phalacrocorax aristotelis). Partial Least Squares (PLS) analysis showed that fluctuating asymmetry of wing bone length (FA_WBL) was affected by PCB-105, -118, -138, -153, and -180 (r²x = 0.88, r²y = 0.35, q² = 0.29). Bivariate correlation confirmed significant positive relationships between FA_WBL and each of these PCB congeners. In the PLS model no other biological variables were significantly affected by any of the POPs. Levels of POPs were much lower in the shag chicks than in eggs and in hatchlings from the same breeding colony, most likely due to growth dilution of the compounds. We suggest that the effects of the PCBs on FA_WBL may be due to effects of these compounds on bone growth and bone structure. FA_WBL may have functional effects on the fitness if it persists after fledging.     

Effect of moderate pre-oxidation on the removal of Microcystis aeruginosa by KMnO4-Fe(II) process: significance of the in-situ formed Fe(III)

This study developed a novel KMnO₄-Fe(II) process to remove the cells of Microcystis aeruginosa, and the mechanisms involved in have been investigated. At KMnO₄ doses of 0-10.0 μM, the KMnO₄-Fe(II) process showed 23.4-53.3% higher efficiency than the KMnO₄-Fe(III) process did. This was first attributed to the moderate pre-oxidation of M. aeruginosa by KMnO₄, achieved by dosing Fe(II) after a period of pre-oxidation, to cease the further release of intracellular organic matter (IOM) and the degradation of dissolved organic matter (DOM). The extensive exposure of M. aeruginosa to KMnO₄ in KMnO₄-Fe(III) process led to high levels and insufficient molecular weight of DOM, inhibiting the subsequent Fe(III) coagulation. Additionally, Fe(II) contributed to lower levels of the in-situ formed MnO₂, the reduction product of KMnO₄ which adversely affected algae removal by Fe(III) coagulation. However, the in-situ formed Fe(III), which was derived from the oxidation of Fe(II) by KMnO₄, in-situ MnO₂, and dissolved oxygen, dominated the remarkably high efficiency of KMnO₄-Fe(II) process with respect to the removal of M. aeruginosa. On one hand, in-situ formed Fe(III) had more reactive surface area than pre-formed Fe(III). On the other hand, the continuous introduction of fresh Fe(III) coagulant showed higher efficiency than one-off dosage of coagulant to destabilize M. aeruginosa cells and to increase the flocs size. Moreover, the MnO₂ precipitated on algae cell surfaces and contributed to the formation of in-situ formed Fe(III), which may act as bridges to enhance the removal of M. aeruginosa.     

Cu-doped TiO(2) nanoparticles enhance survival of Shewanella oneidensis MR-1 under ultraviolet light (UV) exposure

It has been shown that photocatalytic TiO₂ nanoparticles (NPs) can be used as an efficient anti-microbial agent under UV light due to generation of reactive oxygen species (ROS), while Shewanella oneidensis MR-1 is a metal-reducing bacterium highly susceptible to UV radiation. Interestingly, we found that the presence of Cu-doped TiO₂ NPs in the cultural medium dramatically increased the survival rates (based on colony-forming unit) of strain MR-1 by over 10,000-fold (incubation without shaking) and ~ 200 fold (incubation with shaking) after a 2-h exposure to UV light. Gene expression results (via qPCR measurement) indicated that the DNA repair gene recA in MR-1 was significantly induced by UV exposure (indicating cellular damage under UV stress), but the influence of NPs on recA expression was not statistically evident. Plausible explanations to NP attenuation of UV stresses are: 1. TiO₂ based NPs are capable of scattering and absorbing UV light and thus create a shading effect to protect MR-1 from UV radiation; 2. more importantly, Cu-doped TiO₂ NPs can co-agglomerate with MR-1 to form large flocs that improves cells' survival against the environmental stresses. This study improves our understanding of NP ecological impacts under natural solar radiation and provides useful insights to application of photocatalytic-NPs for bacterial disinfection.     

Denitrification by packed bed reactors in the presence of chromium(VI): Resistance to inhibition

The effect of chromium Cr⁶⁺ on bacterial denitrification was investigated. The long-term influence of chromium presence was observed in packed bed reactors using methanol, ethanol, n-propanol, n-butanol, sec-butanol, tert-butanol, iso-butanol and n-pentanol as the carbon and energy sources for denitrifiers. Short-term influence was investigated by the inhibition coefficient K_i determination within activated sludge under anoxic conditions. The measured inhibition constant K_i was equal to 84.2 mg l^?1 Cr⁶⁺, independently of the kind of organic compound utilized as the electron donor for the bacterial system. The concepts of the reactor resistance to inhibition (RRI) and the resistance to inhibition (RI) have been evaluated.     

Comparative assessment of genotoxicity of mineral water packed in polyethylene terephthalate (PET) and glass bottles

The potential migration of genotoxic compounds into mineral water stored in polyethylene terephthalate (PET) bottles was evaluated by an integrated chemical/biological approach using short-term toxicity/genotoxicity tests and chemical analysis. Six commercial brands of still and carbonated mineral water bottled in PET and in glass were stored at 40 °C for 10 days in a stove according to the standard EEC total migration test (82/711/EEC), or at room temperature in the dark. After treatment, the samples were analysed using gas-chromatography/mass spectrometry (GC/MS) to detect volatile and non-volatile compounds, the Microtox^® test to evaluate potential toxicity of the samples, and three mutagenicity tests - Tradescantia and Allium cepa micronucleus tests and the Comet assay on human leukocytes - to detect their genotoxic activity.GC/MS analysis did not detect phthalates or acetaldehyde in the water samples. The Microtox^® test found no toxic effects. Mutagenicity tests detected genotoxic properties of some samples in both PET and glass bottles. Statistical analyses showed a positive association between mineral content and mutagenicity (micronuclei in A. cepa and DNA damage in human leukocytes). No clear effect of treatment and PET bottle was found. These results suggest the absence of toxic compounds migrating from PET regardless of time and conditions of storage. In conclusion, bottle material and stove treatment were not associated with the genotoxic properties of the water; the genotoxic effects detected in bottled water may be related to the characteristics of the water (minerals and CO₂ content).     

Dynamic multi-phase partitioning of decamethylcyclopentasiloxane (D5) in river water

The behaviour of decamethylcyclopentasiloxane (D5) in river water was evaluated by measuring concentration changes in open beakers. Effective values for the partition coefficient between organic carbon and water (K_OC) were derived by least-squares optimisation of a dynamic model which accounted for partitioning between the sorbed and dissolved phases of D5, and for losses via volatilisation and hydrolysis. Partial mass transfer coefficients for volatilisation were derived from model fits to controls containing deionised water. Effective values of log (K_OC) were between 5.8 and 6.33 (mean 6.16). These figures are higher than some other experimentally-derived values but much lower than those estimated from the octanol: water partition coefficient using single-parameter linear free energy relationships (LFERs). A poly-parameter LFER gave a predicted log (K_OC) of 5.5. Differences in partitioning are believed to be due to the nature of the organic matter present. The new value for effective K_OC was employed in a simple model of D5 behaviour in rivers to ascertain the extent to which a higher affinity for organic carbon would depress volatility. The results suggest that despite the revised K_OC value, volatilisation of D5 remains a significant removal mechanism in surface waters.     

Evaluation of surface roughness of Thai medium density fiberboard (MDF)

Wood composites contain irregularities on their surface due to the sanding process which play an important role when they are used as substrate for thin overlays. The objective of this study is to evaluate surface characteristics of commercially manufactured medium density fiberboard (MDF) panels in Thailand. A skid type profilometer with diamond stylus of 5 μm tip radius and 90° tip angle was employed for the experiment. Roughness average (R_a), average maximum height of the profile (R_z), and maximum roughness depth (R_max) were used to evaluate quantitatively surface characteristics of the specimens. Roughness measurements were taken from both sides of the sanded specimens along and across the sandmarks over 15.2 mm tracing span. Panel type-C had the smoothest surface with average values of 2.39, 21.03, and 26.93 μm for R_a, R_z, and R_max, respectively. It was found that no statistically (p<0.1$p<0.1$) significant difference existed between the values of all three parameters taken in both sandmark directions of all types of panels. Also none of the panels considered in this study had superior surface quality over the other. In further studies, surface roughness of MDF samples exposed to various relative humidity levels could give a better understanding of their roughness behavior for different overlaying applications.     

Sorbents with the structure of layered double hydroxides for aquatic media treatment from U(VI)

Sorbents representing the layered double hydroxides of composition [Mg₄Fe₂(OH)₁₂] ? CO₃ ?nH₂O, [Zn₄Al₂(OH)₁₂] ? CO₃ ? nH₂O, and also the products of their thermal treatment at 400°C intended for the aquatic media treatment from U(VI) have been investigated. It is shown that the high sorption capacity of these sorbents makes it possible to recommend them for the effective removal of U(VI) from waters having different mineral composition.     

Coagulation behavior of Al(13) aggregates

The coagulation behavior of Al₁₃ aggregates formed in coagulation of kaolin was investigated by small angle static light scattering (SASLS), solid-state ²⁷Al NMR and tapping mode atomic force microscope (TM-AFM). A kaolin suspension was coagulated by PACl containing high content of Al₁₃ polycation (PACl-Al₁₃). The results indicated that Al₁₃ was predominant in destabilizing kaolin particles for PACl-Al₁₃ coagulation even though at alkaline pH (pH 10). At such high pH, Al₁₃ aggregates were observed when the dosage of PACl-Al₁₃ was increased. In addition, the mechanism of coagulation by PACl-Al₁₃ at alkaline pH was affected by dosage. When the dosage was insufficient, coagulation was caused by electrostatic patch, which led to compact flocs with high fractal dimension (D_f). Interparticle bridging dominated the coagulation when the coagulant dosage approached the plateau of adsorption, which caused the looser flocs with low D_f. The in-situ AFM scanning in liquid system proved that the existence of linear Al₁₃ aggregates composed of a chain of coiled Al₁₃ in coagulation by PACl-Al₁₃ at a high dosage and alkaline pH. Meanwhile, several coiled Al₁₃ aggregates with various dimensions were observed at such condition.     

New and conventional pore size tests in virus-removing membranes

Microorganisms are retained by ultrafiltration (UF) membranes mainly due to size exclusion. The sizes of viruses and membrane pores are close to each other and retention of viruses can be guaranteed only if the precise pore diameter is known. Unfortunately and rather surprisingly, there is no direct method to determine the membrane pore size. As a result, the UF membranes are not trusted to remove the viruses, and the treatment plants are required to enhance viral disinfection.Here we propose a new, simple and effective method for UF pore size determination using aquasols of gold and silver nanoparticles. We synthesized highly monodispersed suspensions ranging in diameter from 3 to 50 nm, which were later transferred through polymer and ceramic UF membranes. The retention percentage was plotted against the particle diameter to determine the pore size for which a membrane has a retention capability of 50, 90 and 100%. The d₅₀, d₉₀ and d₁₀₀ values were compared with data obtained from conventional transmembrane flux, polyethylene glycol, and dextran tests, and with the retention of phi X 174 and MS2 bacteriophages.The absolute pore size, d₁₀₀, for the majority of tested UF membranes is within 40-50 nm, and can only be detected with the new tests. The average 1.2 log retention of hydrophilic phi X 174 was predicted accurately by models based on the virus hydrodynamic radii and d₁₀₀ pore size. The 2.5 log MS2 retention suggests hydrophobic interactions in addition to simple ball-through-cylinder geometry.     

Implications of organic matter on arsenic mobilization into groundwater: Evidence from northwestern (Chapai-Nawabganj), central (Manikganj) and southeastern (Chandpur) Bangladesh

Boreholes (50 m depth) and piezometers (50 m depth) were drilled and installed for collecting As-rich sediments and groundwater in the Ganges, Brahmaputra, and Meghna flood plains for geochemical analyses. Forty-one groundwater samples were collected from the three areas for the analyses of cations (Ca²⁺, Mg²⁺, K⁺, Na⁺), anions (Cl⁻, NO₃⁻, SO₄²⁻), total organic carbon (TOC), and trace elements (As, Mn, Fe, Sr, Se, Ni, Co, Cu, Mo, Sb, Pb). X-ray powder diffraction (XRD) and X-ray fluorescence (XRF) were performed to characterize the major mineral and chemical contents of aquifer sediments. In all three study areas, results of XRF analysis clearly show that fine-grained sediments contain higher amounts of trace element because of their high surface area for adsorption. Relative fluorescent intensity of humic substances in groundwater samples ranges from 30 to 102 (mean 58 ± 20, n = 20), 54-195 (mean 105 ± 48, n = 10), and 27-243 (mean 79 ± 71, n = 11) in the Ganges, Brahmaputra and Meghna flood plains, respectively. Arsenic concentration in groundwater (20-50 m of depth) ranges from 3 to 315 μg/L (mean 62.4 ± 93.1 μg/L, n = 20), 16.4-73.7 μg/L (mean 28.5 ± 22.4 μg/L, n = 10) and 4.6-215.4 μg/L (mean 30.7 ± 62.1 μg/L, n = 11) in the Ganges, Brahmaputra and Meghna flood plains, respectively. Specific ultra violet adsorption (SUVA) values (less than 3 m⁻¹ mg⁻¹ L) indicate that the groundwater in the Ganges flood plain has relatively low percentage of aromatic organic carbon compared to those in the Brahmaputra and Meghna flood plains. Arsenic content in sediments ranges from 1 to 11 mg/kg (mean 3.5 ± 2.7 mg/kg, n = 17) in the three flood plains. Total organic carbon content is 0.5-3.7 g/kg (mean 1.9 ± 1.1 g/kg) in the Ganges flood plain, 0.5-2.1 g/kg (mean: 1.1 ± 0.7 g/kg) in the Brahmaputra flood plain and 0.3-4.4 g/kg (mean 1.9 ± 1.9 g/kg) in the Meghna flood plain. Arsenic is positively correlated with TOC (R² = 0.50, 0.87, and 0.85) in sediments from the three areas. Fourier transform infrared (FT-IR) analysis of the sediments revealed that the functional groups of humic substances in three areas include amines, phenol, alkanes, and aromatic carbon. Arsenic and Fe speciation in sediments were determined using XANES and the results imply that As(V) and Fe(III) are the dominant species in most sediments. The results also imply that As (V) and Fe (III) in most of the sediment samples of the three areas are the dominant species. X-ray absorption fine structure (EXAFS) analysis shows that FeOOH is the main carrier of As in the sediments of three areas. In sediments, As is well correlated with Fe and Mn. However, there is no such correlation observed between As and Fe as well as As and Mn in groundwater, implying that mobilizations of Fe, Mn, and As are decoupled or their concentrations in groundwater have been affected by other geochemical processes following reductive dissolution of Fe or Mn-hydroxides. For example, dissolved Fe and Mn levels may be affected by precipitation of Fe- and Mn-carbonate minerals such as siderite, while liberated As remains in groundwater. The groundwaters of the Brahmaputra and Meghna flood plains contain higher humic substances in relative fluorescence intensity (or fluorescence index) and lower redox potential compared to the groundwater of Ganges flood plain. This leads to the release of arsenic and iron to groundwater of these three plains in considerable amounts, but their concentrations are distributed in spatial variations.     

Iron oxide amended biosand filters for virus removal

Laboratory studies were performed to determine if the addition of iron oxides throughout biosand filter (BSF) media would increase virus removal due to adsorption. The proposed mechanism is electrostatic adsorption of negatively charged virion particles to positively charged iron oxides formed during the corrosion of zerovalent iron. Initial tests conducted using continuous flow, small-scale glass columns showed high MS2 bacteriophage removal in an iron-amended sand column (5log₁₀) compared to a sand-only column (0.5log₁₀) over 20 pore volumes. Additionally, two experiments with a column containing iron particles revealed 4log₁₀ and 5log₁₀ removal of rotavirus in the presence of 20 mg/L total organic carbon. Full-scale BSFs with iron particles removed >4log₁₀ MS2 for the duration of the experiment (287 days), while BSF with steel wool removed >4log₁₀ MS2 for the first 160 days. Plug flow for the BSF was shown to depend on uniformity between the iron oxide material and sand media grains. The results suggest that the duration of effective virus removal by iron-amended biosand filtration depends on source water conditions and the quantity and composition of iron material added. Overall, this study provides evidence that iron-amended BSFs may advance the field of point-of-use technologies and bring relief to millions of people suffering from waterborne diseases.     

The acute lethal toxicity of heavy metals to peracarid crustaceans (with particular reference to fresh-water asellids and gammarids)

In static tests on the acute toxicity of metal salts to two fresh-water peracarids, Asellus aquaticus (L.) (Isopoda) and Crangonyx pseudogracilis Bousfield (Amphipoda), 48 and 96 h LC₅₀ values were determined for Al(III), Cd(II), Cr(III), Cu(II), Fe(III), Hg(II), Mn(II), Ni (II), Pb(II) and Zn(II). Additional metals tested upon Crangonyx alone were Ag(I), Co(II), Cr(VI), Fe(II), Mn(VII), Mo(VI), Sn(II) and V(V). Of the metal salts tested on both species, Asellus was more sensitive to Al(III) and Mn(II) than Crangonyx, similarly sensitive to Cd(II), Fe(III) and Zn(II), and less sensitive to the remainder. Toxicity of metal salts which are unstable with respect to reduction or oxidation was found to be higher than that of the corresponding stable salts of the same metal.Previously published data on the acute toxicity of heavy metal salts to fresh-water, estuarine and marine amphipods and isopods are tabulated and discussed. Brief comparisons are also made between the relative tolerances of peracarids, Daphnia and fresh-water fish. Crangonyx pseudogracilis is recommended as worthy of further research, due to its widespread distribution and ease of culture.     

Gas transport parameters of differently compacted granulated bentonite mixtures (GBMs) under air-dried conditions

Granulated bentonite mixtures (GBMs) have been regarded as effective buffer materials in the deep geological disposal of radioactive waste due to their operational advantages, such as ease of transportation and in-situ placement/backfilling. Many studies have been done to characterize the hydraulic and thermal properties of GBMs as well as their swelling properties. Only limited studies, however, have investigated their gas transport properties, even though these properties affect their compactness during in-situ placement/backfilling and subsequent gas diffusion and advection in the buffer zone. The aim of this study is to understand the gas transport parameters, i.e., air permeability (k_a) and gas diffusivity (D_p/D_o), of tested samples compacted at different dry densities (DDs) under air-dried conditions, linking them with the measured density distribution characteristics determined by microfocus X-ray computed tomography (MFXCT) analysis. Two types of GBMs were used in this study: 1) FE-GBM (prepared from National Standard® bentonite, Wyoming, USA): this material was used in the Full-scale Emplacement (FE) experiment at the Mont Terri rock laboratory, Switzerland) and 2) OK-GBM (prepared from a bentonite, originating from Japan, with the trade name of OK bentonite, Kunimine Industries). The tested samples were firstly packed in a 100-cm³ acrylic core with different DDs, ranging from loose to dense (1.09 to 1.75 g/cm³), and scanned by MFXCT. The weighting factors, w_f (fine fraction; lower density) and w_c (coarse fraction; higher density) (w_f + w_c = 1), were determined after the peak separation of the measured CT brightness histograms from the reconstructed three-dimensional multiplanar reconstruction (MPR) images of the MFXCT analysis. The measured k_a and D_p/D_o were highly dependent on the DDs, the k_a (?) values fitted well with a power law model, and the D_p/D_o (?) was predicted accurately by several previously proposed models. For both FE-GBM and OK-GBM, there were good linear relationships between the gas transport parameters and w_c × DD, implying that the weight of the coarse fraction controlled k_a and D_p/D_o. Moreover, the Kozeny-Carman model, incorporating the measured volumetric surfaces from the MFXCT analysis, was able to predict the k_a values well.     

Distribution of the solvent-extractable organic compounds in fine (PM1) and coarse (PM1-10) particles in urban, industrial and forest atmospheres of Northern Algeria

The distribution of the solvent-extractable organic components in the fine (PM₁) and coarse (PM_1-10) fractions of airborne particulate was studied for the first time in Algeria. That was done during October 2006 concurrently in a big industrial district, a busy urban area, and a forest national park located in Algiers, Boumerdes, Blida, respectively, which are the three biggest provinces of Northern Algeria. Most of the organic matter identified in both particle size ranges consisted of n-alkanes and n-alkanoic acids, with minor contributions coming from polycyclic aromatic hydrocarbons (PAHs), nitrated polycyclic aromatic hydrocarbons (NPAHs), oxygenated PAHs, and other polar compounds (e.g., caffeine and nicotine). The potential emission sources of airborne contaminants were reconciled by combining the values of n-alkane carbon preference index (CPI) and selected diagnostic ratios of PAHs, calculated in both size ranges. The mean cumulative concentrations of PAHs reached 3.032 ng m^− 3 at the Boumerdes site, urban, 80% of which (i.e. 2.246 ng m^− 3) in the PM₁ fraction, 6.462 ng m^− 3 at Rouiba-Réghaia, industrial district, (5.135 ng m^− 3 or 80% in PM₁), and 0.512 ng m^− 3 at Chréa, forested mountains (0.370 ng m^− 3 or 72% in PM₁). Similar patterns were shown by all organic groups, which resulted overall enriched in the fine particles at the three sites. Carcinogenic and mutagenic potencies associated to PAHs were evaluated by multiplying the concentrations of “toxic” compounds times the corresponding potency factors normalized vs. benzo(a)pyrene (BaP), and were found to be both acceptable.     

Removal of As(III) and As(V) by Tin(II) compounds

The retention capacity for arsenic species of new nanomaterials based on tin(II) inorganic oxides or hybrid (inorganic and organic) materials was studied. The synthesis of a polymer-metal complex was performed with poly(acrylic acid) and tin(II) chloride. Poly(AA)-Sn(II) with 10 and 20 wt% of tin and a structure with a mol ratio tin:carboxylate group of 1:1, were characterized. These compounds with 10 and 20 wt% of tin content were used to compare the arsenic removal capability through the liquid-phase polymer-based retention, (LPR), technique. Also, tin oxide was prepared by adding alkaline solution to tin(II) chloride salt. The intermediate tin compound was studied by UV-Vis spectroscopy at different pH values and quantified by potentiometric titration. The solid structure is characterized by Fourier transformed infrared spectroscopy, X-ray diffraction, and specific area BET (N₂). Removal of arsenite and arsenate species from solution by hydrolysated tin was carried out by LPR technique with ultrafiltration membranes and a fixed-bed column unsupported or supported on SiO₂. In all these cases, a washing method at constant pH was applied. The arsenic retention ability depended on the class of tin compounds prepared, with a higher efficiency for arsenic being observed at basic pH for soluble complex poly(AA)-Sn(II) than that for tin hydroxide or hydrolysate of Sn⁺².     

Curved concrete filled steel tubular (CCFST) built-up members under axial compression: Experiments

A series of tests on curved concrete filled steel tubular (CCFST) built-up members subjected to axial compression is described in this paper. Twenty specimens, including 18 CCFST built-up members and 2 curved hollow tubular built-up columns, were tested to investigate the influence of variations in the tube shape (circular and square), initial curvature ratio (β_r, from 0 to 7.4%), nominal slenderness ratio (λ_n, from 9.9 to 18.9), section pattern (two main components, three main components and four main components), as well as brace pattern (battened and laced) on the performance of such composite built-up members. The experimental results showed that the ultimate strength and stiffness of CCFST built-up specimens decreased with increasing β_r or λ_n. Different load-bearing capacities and failure modes were obtained for the battened and laced built-up members. A simplified method using an equivalent slenderness ratio was suggested to calculate the strength of CCFST built-up members under axial compression.