Model Simulation of Diurnal Vertical Migration Patterns of Different-Sized Colonies of Microcystis Employing a Particle Trajectory Approach.

Microcystis, a genus of potentially harmful cyanobacteria, is known to proliferate in stratified freshwaters due to its capability to change cell density and regulate buoyancy. In this study, a trajectory model was developed to simulate the cell density change and spatial distribution of Microcystis cells with nonuniform colony sizes. Simulations showed that larger colonies migrate to the near-surface water layer during the night to effectively capture irradiation and become heavy enough to sink during daytime. Smaller-sized colonies instead took a longer time to get to the surface. Simulation of the diurnally varying Microcystis population profile matched the observed pattern in the field when the radii of the multisized colonies were in a beta distribution. This modeling approach is able to take into account the history of cells by keeping track of their positions and properties, such as cell density and the sizes of colonies. It also serves as the basis for further developmental modeling of phytoplanktons that are forming colonies and changing buoyancy.

Biodegradable surfactant stabilized nanoscale zero-valent iron for in situ treatment of vinyl chloride and 1,2-dichloroethane.

Nanoscale zero-valent iron (NZVI) stabilized with dispersants is a promising technology for the remediation of contaminated groundwater. In this study, we demonstrated the use of biodegradable surfactant stabilized NZVI slurry for successful treatment of vinyl chloride (VC) and 1,2-dichloroethane (1,2-DCA) in a contaminated site in Taiwan. The biodegradable surfactant stabilized NZVI was coated with palladium and synthesized on-site. From monitoring the iron concentration breakthrough and distribution, it was found that the stabilized NZVI is capable of transporting in the aquifer at the test plot (200 m(2)). VC was effectively degraded by NZVI while the 1,2-DCA degradation was relatively sluggish during the 3-month field test. Nevertheless, as 1,2-DCA is known to resist abiotic reduction by NZVI, the observation of 1,2-DCA degradation and hydrocarbon production suggested a bioremediation took place. ORP and pH results revealed that a reducing condition was achieved at the testing area facilitating the biodegradation of chlorinated organic hydrocarbons. The bioremediation may be attributed to the production of hydrogen gas as electron donor from the corrosion of NZVI in the presence of water or the added biodegradable surfactant serving as the carbon source as well as electron donor to stimulate microbial growth.

Simultaneous estimation of glass-water distribution and PDMS-water partition coefficients of hydrophobic organic compounds using simple batch method.

A simple batch method by use of refilling and nonrefilling experimental procedures and headspace solid phase microextraction was applied to simultaneously obtain the glass-water distribution coefficients (K(GW)) and polydimethylsiloxane(PDMS)-water partition coefficients (K(PW)) of hydrophobic organic compounds (HOCs). The simple batch method takes into consideration the glass-surface bound HOCs and the corresponding equilibrium distribution of HOCs among the glass, water, headspace, and polydimethylsiloxane (PDMS). The K(PW) and K(GW) values of 53 PCB congeners were determined. The glass-bound fraction predominated over other fractions for highly chlorinated PCBs. Ignoring glass adsorption and assuming a complete mass balance could thus substantially underestimate the K(PW) for HOCs in traditional work. Good linear correlations of logα (the overall mass transfer rate constant) vs logK(PW), logK(PW) vs logK(OW), and logK(GW) vs logK(OW) were observed, with logα = -0.91 logK(PW) + 1.13, R(2) = 0.93; logK(PW) = 1.032 logK(OW) - 0.493, R(2) = 0.947; and logK(GW) = 0.93 logK(OW) - 2.30, R(2) = 0.90. The K(PW) values from this study were compared with those in the literature. With an account of the glass adsorption, the accuracy of the K(PW) determination and the estimation of the dissolved concentration in water for highly hydrophobic compounds can be significantly improved.

Development of a trajectory model for predicting attachment of submicrometer particles in porous media: stabilized NZVI as a case study.

A new trajectory simulation algorithm was developed to describe the efficiency of a single collector (pore) to catch submicrometer particles moving through saturated porous media. A constricted-tube model incorporating the deterministic (interception, hydrodynamic retardation, van der Waals force and gravitational sedimentation), stochastic (Brownian diffusion), and thermodynamic (electrostatic and steric repulsion force) mechanisms was established to predict the transport and deposition of surface modified nanoscale zerovalent iron (NZVI) particles by applying Lagrangian trajectory analytical approach. The simulation results show good agreement with the results predicted by existing energy-barrier-free models except for the particle size less than 100 nm at low approach velocity. The number of realizations per start location could be decreased down to 100 with the simulations still exhibiting acceptable relative standard deviation for engineering purposes. With the consideration of energy barriers, the model successfully describes the breakthrough curve of polymer-modified NZVI in a benchtop soil column as well. The novel simulation scheme can be a useful tool for predicting the behavior of the nanoscale colloidal particles moving through filter beds or saturated soil columns under conditions with repulsion and attraction forces among surfaces.

Stability of metal oxide nanoparticles in aqueous solutions.

The application of nanoparticles in the processes of making commercial products has increased in recent years due to their unique physical and chemical properties. With increasing amount of commercial nanoparticles released into nature, their fate and effects on the ecosystem and human health are of growing concern. This study investigated the stability and morphology of three metal oxide nanoparticles in aqueous solutions. The commercially available nanoparticles, TiO(2), ZnO, SiO(2), aggregated quickly into micrometer-size particles in aqueous solutions, which may not threaten human health. Their changes in morphology and characteristics were further examined by dynamic light scattering (DLS) method and transmission electron microscopy (TEM). Among the several dispersion approaches, ultrasonication was found to be the most effective for disaggregating nanoparticles in water. For these three selected nanoparticles, ZnO could not remain stable in suspensions, presumably due to the dissolution of particles to form high concentration of ions, resulting in enhanced aggregation of particles. In addition, the existence of dissolved organic matters stabilized nanoparticles in lake water and wastewater for several hours in spite of the high concentration of cations in these real-water samples. The fate of metal oxide nanoparticles in natural water bodies would be determined by the type and concentration of cations and organic matters. Results obtained in this study revealed that the stability of nanoparticles changed under different aqueous conditions and so did their fate in the environment.

Influence of nanoscale zero-valent iron on geochemical properties of groundwater and vinyl chloride degradation: A field case study.

A 200m(2) pilot-scale field test successfully demonstrated the use of nanoscale zero-valent iron (NZVI) for effective remediation of groundwater contaminated with chlorinated organic compounds in Taiwan within six months. Both commercially available and on-site synthesized NZVI were used. A well-defined monitoring program allowing to collect three-dimensional spatial data from 13 nested multi-level monitoring wells was conducted to monitor geochemical parameters in groundwater. The degradation efficiency of vinyl chloride (VC) determined at most of monitoring wells was 50-99%. It was found that the injection of NZVI caused a significant change in total iron, total solid (TS) and suspended solid (SS) concentrations in groundwater. Total iron concentration showed a moderate and weak correlation with SS and TS, respectively, suggesting that SS may be used to indicate the NZVI distribution in groundwater. A decrease in oxidation-reduction potential (ORP) values from about -100 to -400mV after NZVI injection was observed. This revealed that NZVI is an effective means of achieving highly reducing conditions in the subsurface environment. Both VC degradation efficiency and ORP showed a correlative tendency as an increase in VC degradation efficiency corresponded to a decrease of ORP. This is in agreement with the previous studies suggesting that ORP can serve as an indicator for the NZVI reactivity.

Characterization and composition of heavy metals and persistent organic pollutants in water and estuarine sediments from Gao-ping River, Taiwan.

The objective of this study was to determine the concentrations and possible sources of heavy metals and persistent organic pollutants (POPs) in water and estuarine sediments from Gao-ping River in order to evaluate the environmental quality of aquatic system in southern Taiwan. High concentrations of heavy metals including Cr, Zn, Ni, Cu and As, ranging from 10.7 to 180 mg/kg-dry weight (dw), were detected in sediments from Gao-ping River. When normalized to the principal component analysis (PCA), swinery and electroplating wastewaters were found to be the most important pollution sources for heavy metals. Of various organochlorine pesticide (OCP) residues detected, aldrin and total-hexachlorocyclohexane (HCH) were frequently found in sediments. The total concentrations of OCPs were in the range 0.47-47.4 ng/g-dw. Also, the total-HCH, total-cyclodiene, and total-dichlorodiphenyltrichloroethane (DDT) were in the range 0.37-36.3, 0.21-19.0, and 0.44-1.88 ng/g-dw, respectively. The polychlorinated biphenyl (PCB) concentrations in sediments from Gao-ping River ranged between 0.37 and 5.89 ng/g-dw. The PCB concentrations are positively correlated to the organic contents of the sediment particles. alpha-HCH was found to be the dominant compound of HCH in the sediments, showing that long-range transport may be the possible source for the contamination of HCH in sediments from Gao-ping River. In summary, trace amounts of POPs in estuarine sediments from Gao-ping River were detected, showing that there still exist a wide variety of POP residues in the river sediments in Taiwan. These POP residues may be mainly from long-range transport and weathered agricultural soils, while heavy metal contamination is primarily from the swinery and industrial wastewaters.

Sorption kinetics of toluene in humic acid: a computational approach.

Molecular dynamics, a computational technique aiming to describe the time-dependent movement of molecules, has been applied to study the sorption kinetics of volatile organic contaminants in soil organic matter. The molecular dynamics simulation results obtain reasonably accurate estimates of diffusion rates and activation energy of the penetration of a volatile organic compound molecule into a model humic substance. The sorption rate of toluene to humic acid decreases with the density of the humic acid matrix and increases with temperature. All the present results indicate that the sorption of toluene into humic acid is mainly diffusion controlled. Finally, the present studies have shown that molecular dynamics of volatile organic compounds in humic substances yields meaningful results, which help in the understanding of diffusion at the molecular level and which facilitate the problem-solving capability for removing the contaminants from the soils.

Seasonal variation of the distribution of PCBs in sediments and biota in a PCB-contaminated estuary.

To elucidate the effects of seasonal variation of precipitation on the distribution of polychlorinated biphenyls (PCBs) in estuarine sediments and benthic feeders, PCB concentrations of river surface sediments and mullet fish (Liza macrolepis) were investigated in the estuary of Er-Jen River near former PCB contamination sites before and after each wet season from 2002 to 2004. Analyses of grain size distribution and organic matter revealed that the pre-existing surface sediments were covered by and mixed with the soil particulates brought by surface runoff after each wet season. Obvious increment of PCB content and significantly elevated fraction (p<0.005) of light PCBs of the river mouth's sediments after each wet season indicated that the invading particles were rich in un weathered PCBs. PCBs previously buried in the surface soil of heavily contaminated sites were flushed into this estuary through surface runoff. The precipitation altered the PCB patterns in sediment organic matter, the dietary source of mullet, and consequently changed that of mullets accordingly, which all possessed significant greater fraction of light PCBs. In this study, it was demonstrated that seasonal summer precipitation affected the distribution of PCBs on surface sediments and the mullets of this estuary. PCB residuals retained in this region still pose potential threats to biota resided here.

Bioaccumulation of polychlorinated biphenyls in mullet fish in a former ship dismantling harbour, a contaminated estuary, and nearby coastal fish farms.

This study investigated the bioaccumulation of polychlorinated biphenyls (PCBs) toward mullet fish (Liza macrolepis) living in former PCB contaminated areas, the Ann-Ping harbour and the Er-Jen estuary, and fish farms located near the above two areas in 2003. The PCB body burdens of collected fish samples are proportional to the contamination level of their locations with the following rank order (greatest to least) from the Er-Jen estuary, the Ann-Ping harbour to the fish farms. Concentration of PCBs of the estuarine mullet has been approximately decreased to one-half of the peak concentration of the 1990s. Although the concentration of PCBs in farmed fish inhabiting near the two contaminated areas was greater than the average of those of fish from local fish markets in Taiwan, no particularly great contamination level was observed in their bodies. Using the less chlorinated PCB fraction (triCB + tetraCB)/total PCBs as the indicator of the origins of PCBs, fish near former contaminated areas had greater body burdens of the more chlorinated PCB congeners, while the farmed fish exhibited a PCB pattern more like that known to originate from air-water exchange with less chlorinated PCBs predominating. Although the PCB contamination has been stopped for a decade, the residual contaminants, supposedly existing in soil and sediments, still contribute to the body burden of fish residing in the estuary and the harbour.

Distinctive sorption mechanisms of soil organic matter and mineral components as elucidated by organic vapor uptake kinetics.

Sorption kinetics and capacities of volatile organic compounds (VOCs) affect the remediation and fate of these pollutants in soils. The soil organic-mineral compositional heterogeneity complicates the transport and fate of VOCs in soils. The sorption kinetics of toluene vapor with two common soil components, kaolinite and humic acid, shows two distinct sorption patterns. Results with kaolinite are characteristic of surface adsorption, whereas results with humic acid are characteristic of solvation and partition effects. On soils, the kinetics of toluene vapor sorption show a two-stage sorption phenomenon. The first stage is reflective of surface adsorption (1-4 h to completion) and the second stage of much slower partitioning into soil organic matter, which was preceded by a lag phase (approximately 4 h) and took as long as 15 h for completion. The relative contributions of these two stages to soil uptake are quantifiable by two independent parameters, the soil organic fraction and the surface area. A better understanding of the effect of soil compositional heterogeneity on sorption kinetics and capacities facilitates our understanding of the prediction for the fate of organic contaminants in the environment.

Kinetics of toluene sorption and desorption in Ca- and Cu-montmorillonites investigated with Fourier transform infrared spectroscopy under two different levels of humidity.

Clays in soils or groundwater aquifer materials play roles in the sorption of organic pollutants. The intrinsic sorption kinetics of toluene in dry and humid clay films was investigated by tracking the change of infrared absorbance. Under the humid condition, similar toluene-sorbed intensities were found in Ca- and Cu-montmorillonites. However, a higher intensity of sorbed toluene was found in the Cu-form than in the Ca-form under the dry condition, which indicates a stronger interaction occurring in dry Cu-montmorillonite. The general time scale of sorption of toluene on clays is around 100 s. In both forms of montmorillonite, some portion of toluene was desorbed at an extremely slow rate under the dry condition. Some newly identified peaks were persistent against desorption from montmorillonites, suggesting the existence of irreversibly sorbed species and the possibility of toluene transformation occurring in clay systems.

Infrared investigation of the sequestration of toluene vapor on clay minerals.

The Ca-exchanged clays were used to investigate the sorption of toluene under both high and low relative humidity conditions. According to the observed rates of sorption and desorption and the Fourier transform infrared (FTIR) spectra of sorbed toluene, the sorbate molecules on clays can be divided into three categories: labile (gaslike) phase, slow sorption (liquidlike) phase, and resistant-to-desorption phase with sorption/desorption time scales of less than 30 min, several hours, and several weeks, respectively. Aging changed the spectroscopic characteristics of the sorbed sorbates and contributed to the irreversibility of the sorption under both high and low relative humidity. Irreversibly sorbed portions of the sorbates and new characteristic peaks identified with FTIR spectrometry suggest the existence of chemical transformation of sorbed species under both high and low relative humidity conditions. It is suggested that the clay minerals, acting as catalysts, may contribute to abiotic natural attenuation of volatile organic aromatic hydrocarbons in soils.

Sorption kinetics of selected volatile organic compounds in humin.

Each component of the chemically heterogeneous soil exhibits a unique sorption behavior toward organic sorbates. The sorption kinetics of some volatile organic compounds (VOCs) in pressed humin disks was investigated by tracking the weight change of the disks with a microbalance. Higher sorbing capacity for more polar VOCs as well as C13 nuclear magnetic resonance data indicates that humin was more hydrophilic than Aldrich humic acid (Milwaukee, WI, USA). The apparent diffusivity of acetone, toluene, and hexane in the disks ranged from 10(-8) to 10(-10) cm2/s. The sorbed toluene in humin does not seem persistent to desorption; however, acetone and hexane, either as polar or linear compounds in humin, show persistence against desorption. On completion of the desorption experiments, there were approximately 35 and 20% sorbate residue for acetone and hexane, respectively.

Distribution and fate of organochlorine pesticide residues in sediments from the selected rivers in Taiwan.

The contamination of organochlorine pesticides (OCPs) in sediments from selected rivers in Taiwan was investigated to evaluate the pollution potentials and hazard in river sediments. Da-han River and Erh-jen River were selected as the target rivers due to their serious pollution. A total of 40 surface sediment samples were collected at five sampling stations along the rivers. Results showed that the concentrations of various pesticides in sediments were in the range of 0.57-14.1 ng/g for sigmaHCH, 0.05-0.15 ng/g for aldrin, 0.12-5.8 ng/g for dieldrin, 0.22-0.64 for endrin, 0.24-6.37 ng/g for endosulfan and 0.21-8.81 ng/g for EDDT (p,p'-DDD, p,p'-DDE, p,p'-DDT). Among the OCPs, sigmaHCH, endosulfan and sigmaDDT were the most dominant compounds in the river sediments. Endosulfan sulfate was the most frequent detected compound in the sediments from the selected rivers. Also, sigmaDDT, dieldrin and beta-HCH were in abundance. Different contamination patterns between the selected river sediments were also observed. Da-han River was mainly contaminated with endosulfan sulfate and sigmaDDT. Whereas the main pesticides in Erh-jen River were beta-HCH and sigmaDDT. Among the cyclodiene compounds, dieldrin was in abundance in most of the sediments. Moreover, the frequencies of detection of the metabolites were higher than those of parent compounds, depicting that the sediments have contaminated for a long time. The results obtained in this study showed that there still exist a variety of OCP residues in the river sediments in Taiwan.

Sorption kinetics of toluene in humin under two different levels of relative humidity.

To identify any resistant fraction for desorption of toluene from humin and to quantify the sorption-desorption rates, the time courses of toluene sorption to compressed humin disks and to a thin humin film were investigated. The apparent diffusivity of toluene with humin disks ranges from 10(-8) to 10(-9) cm2/s and increases with temperature, based on the weight change of humin disks mounted on a microbalance and on the results simulated by use of a diffusion model. No detectable level of residual toluene was found after desorption, as revealed either by the gravimetric analysis or by the Fourier transform infrared (FTIR) spectrum obtained at either low or high humidity. The time scale for intrinsic vapor sorption without mass transfer hindrance is less than a few minutes with the thin film. All the results indicate that the sorption of toluene to humin is reversible and mainly diffusion controlled. This finding helps to better understand the sorption kinetics associated with humin and soil organic matter.