102 research outputs found

    Effects of source and seasonal variations of natural organic matters on the fate and transport of CeO2 nanoparticles in the environment

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    Natural organic matter (NOM) affects the stability and transport of nanoparticles (NPs) in natural waters by modifying their physiochemical properties. Source location, and seasonal variations, influence their molecular, physical and electrical charge properties. To understand the variations of NOM on the mobilization of NPs, large volumes of water were collected fromthe Ohio River (OR) over winter and summer seasons and dissolved NOMs were concentrated. The chemical and structural differences of these NOMs were compared with the Suwannee River humic acid (SRHA) SRHA using 1H and 13C nuclear magnetic resonance spectroscopy, and Fourier transforms infrared (FTIR) spectroscopy. Thermal analysis and FTIR confirmed that differences in composition, structure, and functional groups are a result of SRHA fractionation compared to wholemolecule OR-NOM. The influence of OR-NOMs on the surface charge of CeO2NPs and the effects on the transport and retention in a three-phase (deposition-rinse-re-entrainment) sand-packed columns were investigated at CeO2 NPs initial concertation of 10 ppm, pH 6.8, increasing ionic strength (3, 5, and 10 mM), retention time of 1 min, and increasing NOM concentration (1, 5, and 10 ppm). The summer OR-NOM showed higher stabilization and mobilization effect on the CeO2 than the winter NOM; while their effect was very different form the SRHA. The stabilization of NPs is attributed to both electrostatic and steric effects. The differences in the chemical structure of the complex and heterogeneous NOMs showed disparate reactivity and direct impact on CeO2-NPs stability. Using SRHA to study the effect of NOMfor drinkingwater related assessment does not sufficiently represent the natural conditions of the environment

    Selective Oxidation Using Flame Aerosol Synthesized Iron and Vanadium-Doped Nano-TiO 2

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    Selective photocatalytic oxidation of 1-phenyl ethanol to acetophenone using titanium dioxide (TiO2) raw and doped with Fe or V, prepared by flame aerosol deposition method, was investigated. The effects of metal doping on crystal phase and morphology of the synthesized nanostructured TiO2 were analyzed using XRD, TEM, Raman spectroscopy, and BET nitrogen adsorbed surface area measurement. The increase in the concentration of V and Fe reduced the crystalline structure and the anatase-to-rutile ratios of the synthesized TiO2. Synthesized TiO2 became fine amorphous powder as the Fe and V concentrations were increased to 3 and 5%, respectively. Doping V and Fe to TiO2 synthesized by the flame aerosol increased photocatalytic activity by 6 folds and 2.5 folds, respectively, compared to that of pure TiO2. It was found that an optimal doping concentration for Fe and V were 0.5% and 3%, respectively. The type and concentration of the metal dopants and the method used to add the dopant to the TiO2 are critical parameters for enhancing the activity of the resulting photocatalyst. The effects of solvents on the photocatalytic reaction were also investigated by using both water and acetonitrile as the reaction medium

    Recent updates on ions and nutrients uptake by halotolerant freshwater and marine microalgae in conditions of high salinity

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    Algae is an appropriate natural resource to augment the optimal use of undesired ions in water and wastewater. Increasing algal cells, the consumption of particular ions, including chloride, nitrate, phosphate, and ammonium, provides a suitable way to optimize water treatment processes. Different algal species have the capability to survive in extreme salinities by developing resistance against osmotic pressure in saline water. The current study reviews the effect of salinity on algal biomass production, algal growth rate, chlorides, nitrates, phosphates, chemical oxygen demand (COD), total nitrogen, total phosphorus, and ammonium ions. Mainly algae cultivated in freshwater, synthetic brackish water, seawater, and hypersaline water, were studied for this review. Various ion uptake mechanisms used by the algal cell are summarized, focusing on biosorption and bioaccumulation processes. Critical parameters such as light intensity, pH, and temperature variations significantly influence ion and nutrients uptake efficiencies. Analysis performed on collected data indicated that halophytic algae could survive in high salinities at elevated growth rates compared to freshwater. The halotolerant algal species showed an inclining trend of chloride ion removal with an elimination capacity of 7.5 g.m-3.h-1. Moreover, the nitrate uptake rate in halophytic algae is 10-folds higher to phosphate, regardless of salinity level. It could be concluded that microalgae will be beneficial for ion and nutrient uptake processes in treating high saline water

    Supercritical Fluid (SCF) Treatment: Its Effect on Bending Strength and Stiffness of Ponderosa Pine Sapwood

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    Adverse effects on mechanical properties from using a supercritical fluid (SCF) to increase preservative penetration of refractory woods were evaluated by treating small ponderosa pine sapwood specimens with supercritical carbon dioxide at 64 combinations of temperatures (35 to 80 C), pressure (1,000 to 4,000 psig), and time (0.5 to 2 h). Thereafter, the treated and identical untreated specimens were equilibrated to constant moisture content and tested for bending strength and stiffness. The SCF-treated and untreated specimens were not significantly different in modulus of rupture (MOR) or modulus of elasticity (MOE). Temperature, pressure, and time had no significant effect on MOR; there were interacting effects of these variables on MOE, although these interactions had no meaningful patterns

    Supercritical Fluid (SCF) Treatment: Its Effect on Bending Strength and Stiffness of Ponderosa Pine Sapwood

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    Adverse effects on mechanical properties from using a supercritical fluid (SCF) to increase preservative penetration of refractory woods were evaluated by treating small ponderosa pine sapwood specimens with supercritical carbon dioxide at 64 combinations of temperatures (35 to 80 C), pressure (1,000 to 4,000 psig), and time (0.5 to 2 h). Thereafter, the treated and identical untreated specimens were equilibrated to constant moisture content and tested for bending strength and stiffness. The SCF-treated and untreated specimens were not significantly different in modulus of rupture (MOR) or modulus of elasticity (MOE). Temperature, pressure, and time had no significant effect on MOR; there were interacting effects of these variables on MOE, although these interactions had no meaningful patterns

    Comparative Study on the Performance of Anaerobic and Aerobic Biotrickling Filter for Removal of Chloroform

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    Use of biotrickling filter (BTF) for gas phase treatment of volatile trihalomethanes (THMs) stripped from water treatment plants could be an attractive treatment option. The aim of this study is to use laboratory-scale anaerobic BTF to treat gaseous chloroform (recalcitrant to biological transformation) as a model THM and compare results with aerobic BTF. Additional investigations were conducted to determine the microbial diversity present within the BTFs. Chloroform is a hydrophobic volatile THM known to be difficult to biodegrade. To improve the degradation process, ethanol was used as a cometabolite at a different ratio to chloroform. The experimental plan was designed to operate one BTF under anaerobic condition and the other one under aerobic acidic condition. Higher elimination capacity (EC) of 0.23 ± 0.01 g/[m3·h] was observed with a removal efficiency of 80.9% ± 4% for the aerobic BTF operating at pH 4 for the concentration ratio of 1:40 chloroform to ethanol. For similar ratio, the anaerobic BTF supported lower removal efficiency of 59% ± 10% with corresponding lower EC of 0.16 ± 0.01 g/[m3·h]. Carbon recovery acquired for anaerobic and aerobic BTFs was 59% and 63%, respectively. The loading rate for chloroform on both BTFs was 0.27 g/[m3·h] (per m3 of filter bed volume). Variations of the microbial community were attributed to degradation of chloroform in each BTF. Azospira oryzae and Azospira restrica were the dominant bacteria and potential candidates for chloroform degradation for the anaerobic BTF, whereas Fusarium sp. and Fusarium solani were the dominant fungi and potential candidates for chloroform degradation in the aerobic BTF

    Study Of Legionella Pneumophila Treatment With Copper In Drinking Water By Single Cell-ICP-MS

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    Legionella pneumophila is a persistent opportunistic pathogen that poses a significant threat to domestic water systems. Previous studies suggest that copper (Cu) is an effective antimicrobial in water systems. A rapid and sensitive quantification method is desired to optimize the conditions of L. pneumophila treatment by Cu and to better understand the interaction mechanisms between Cu and cells. In this study, we developed a highly sensitive single cell (SC)-ICP-MS method to monitor L. pneumophila cell concentration and track their uptake of Cu. The SC-ICP-MS method showed excellent sensitivity (with a cell concentration detection limit of 1000 cells/mL), accuracy (good agreement with conventional hemocytometry method), and precision (relative standard deviation \u3c 5%) in drinking water matrix. The cupric ions (Cu2+) treatment results indicated that the total L. pneumophila cell concentration, Cu mass per cell, colony-forming unit counting, and Cu concentration in supernatant all exhibited a dose-dependent trend, with 800–1200 µg/L reaching high disinfection rates in drinking water. The investigation of percentages of viable and culturable, viable but nonculturable (VBNC), and lysed cells suggested there always were VBNC present at any Cu concentration. Experimental results of different Cu2+ treatment times further suggested that L. pneumophila cells developed an antimicrobial resistant mechanism with the prolonged Cu exposure. This is the first quantification study on the interactions of Cu and L. pneumophila in drinking water using SC-ICP-MS. Graphical abstract: [Figure not available: see fulltext.
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