James Leckie
C.L. Peck, Class of 1906 Professor in the School of Engineering, Emeritus
Civil and Environmental Engineering
Bio
Leckie investigates chemical pollutant behavior in natural aquatic systems and engineered processes, specifically the environmental aspects of surface and colloid chemistry and the geochemistry of trace elements. New research efforts are focused on the development of techniques and models for assessment of exposure of humans to toxic chemicals. Specific attention has been paid to the evaluation of exposure of young children to toxic chemicals. Other interests include technology transfer and the development of environmental science programs in developing nations.
Academic Appointments
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Emeritus Faculty, Acad Council, Civil and Environmental Engineering
Boards, Advisory Committees, Professional Organizations
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Elected Member, National Academy of Engineering (2013 - Present)
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Appointed Chair Professor in the Department of Environmental Science and Engineering, Tsinghua University, Beijing, China (2013 - Present)
Professional Education
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PhD, Harvard University (1970)
2023-24 Courses
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Independent Studies (10)
- Advanced Engineering Problems
CEE 399 (Aut, Win, Spr, Sum) - Directed Reading or Special Studies in Civil Engineering
CEE 198 (Win, Spr) - Environmental Research
CEE 370B (Win) - Environmental Research
CEE 370C (Spr) - Independent Project in Civil and Environmental Engineering
CEE 199L (Aut, Win, Spr, Sum) - Independent Project in Civil and Environmental Engineering
CEE 299L (Aut, Win, Spr) - Independent Study in Civil Engineering for CEE-MS Students
CEE 299 (Aut, Win, Spr) - Report on Civil Engineering Training
CEE 398 (Aut, Win, Spr, Sum) - Undergraduate Honors Thesis
CEE 199H (Aut, Win, Spr, Sum) - Undergraduate Research in Civil and Environmental Engineering
CEE 199 (Aut, Win, Spr, Sum)
- Advanced Engineering Problems
All Publications
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Quantification and Analysis of Micro-Level Activities Data from Children Aged 1-12 Years Old for Use in the Assessments of Exposure to Recycled Tire on Turf and Playgrounds.
International journal of environmental research and public health
2022; 19 (4)
Abstract
BACKGROUND: There are growing health concerns about exposure to toxicants released from recycled tire rubber, which is commonly used in synthetic turf and playground mats. To better estimate children's exposure and risk from recycled tire rubber used in synthetic turf and playground mats, there is a need to collect detailed accurate information on mouthing activity and dermal contact behaviors. The objective of this study was to quantify and analyze micro-level activity time series (MLATS) data from children aged 1-12 years old while playing (non-sport-related games) at turf-like locations and playgrounds. Another objective was to estimate the incidental ingestion rate of rubber crumb among children.METHODS: Hand and mouth contact frequency, hourly duration, and median contact duration with different objects were calculated for children playing on turf (i.e., parks, lawns, and gardens) (n = 56) and for children playing on playground structures (n = 24). Statistically significant differences between males and females as well as children's age groups were evaluated. The daily incidental ingestion rate of rubber crumb was calculated.RESULTS: For children playing on turf, there were significant differences between younger (1-6 y) and older (7-12 y) children for the mouthing median duration with non-dietary objects and all objects. For children playing on playground structures, we found significant mouthing frequency differences between younger (1-6 y) and older children (7-12 y) with all objects, and for mouthing median duration with non-dietary objects. There were no significant differences between males and females playing on artificial turf-like surfaces or playground mats. Our estimated mean incidental ingestion rate was 0.08, 0.07, and 0.08 g rubber crumb/day for children <2, 2-6, and 6-11 years old, respectively.DISCUSSION: our results suggest that age and contact duration should be considered in risk assessment models to evaluate mouthing activities when children are playing on artificial turf surfaces or playground mats.
View details for DOI 10.3390/ijerph19042483
View details for PubMedID 35206675
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Stochastic Collision-Attachment-Based Monte Carlo Simulation of Colloidal Fouling: Transition from Foulant-Clean-Membrane Interaction to Foulant-Fouled-Membrane Interaction.
Environmental science & technology
2020
Abstract
The initial behavior of colloidal fouling is governed by foulant-clean-membrane interaction (F-M), and its long-term behavior is determined by foulant-fouled-membrane interaction (F-F). Nevertheless, the transitional fouling behavior from F-M to F-F has not been fully understood. This study reports a novel collision attachment (CA)-Monte Carlo (MC) approach, with the stochastic colloid-membrane collision events modeled by MC and the probability of colloidal attachment to the membrane determined by the interplay of flux and the energy barrier arising from colloid-membrane interaction (Em for F-M and Ef for F-F). The long-term membrane flux remains stable for large Ef, whereas severe fouling occurs when both Em and Ef are small. Our study reveals the existence of a metastable flux behavior for the combination of large Em but small Ef. The time evolution of flux behavior and colloidal deposition patterns shows a nearly constant flux for an extended period, with the high energy barrier Em retarding initial colloidal deposition. However, accidental random deposition of a colloidal particle could reduce the local energy barrier (toward the smaller Ef), seeding for further colloidal deposition in its vicinity. This initiates an uneven patch-wise fouling and eventually leads to a complete transition to F-F-dominated behavior. The metastable period can be effectively extended by increasing the energy barrier (Em or Ef) or lowering flux, which provides important implications to membrane design and operation.
View details for DOI 10.1021/acs.est.0c04165
View details for PubMedID 32877173
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Soil ingestion among young children in rural Bangladesh.
Journal of exposure science & environmental epidemiology
2019
Abstract
Ingestion of soil and dust is a pathway of children's exposure to several environmental contaminants, including lead, pesticides, and fecal contamination. Empirically based estimates of central tendency for soil consumption by children in high-income countries range from 9 to 135 dry mg/day. Using a Monte Carlo simulation, we modeled the mass of soildirectly and indirectly ingested per day by rural Bangladeshi children and identified the parameters that influence the mass ingested. We combined data from observations of direct and indirect ingestion among children with measurements of soil mass on the children's hands, mother's hands, and objects to quantify soil ingestion/day. Estimated geometric mean soil ingestion was 162 dry mg/day for children 3-5 months, 224 dry mg/day for children 6-11 months, 234 dry mg/day for children 12-23 months, 168 dry mg/day for children 24-35 months, and 178 dry mg/day for children 36-47 months old. Across all age groups, children placing their hands in their mouths accounted for 46-78% of total ingestion and mouthing objects contributed 8-12%. Direct ingestion of soil accounted for nearly 40% of soil ingested among children 6-23 months old. Sensitivity analyses identified that the parameters most affecting the estimates were the load of soil on the child's hand, the frequency of hand-to-mouth contacts while not eating, and, for children 6-23 months old, the frequency of direct soil ingestion. In a rural, low-income setting, children's soil consumption was substantially more than the estimates for children in high-income countries. Further characterizing soil ingestion of children in low-income contexts would improve assessments of the risks they face from soil-associated contaminants.
View details for DOI 10.1038/s41370-019-0177-7
View details for PubMedID 31673039
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Modeling Dynamics of Colloidal Fouling of RO/NF Membranes with A Novel Collision-Attachment Approach
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2018; 52 (3): 1471–78
Abstract
We report a novel collision-attachment approach for modeling the dynamics of colloidal fouling. The model treats fouling as a two-step process: colloidal particles colliding with a membrane surface followed by their attachment onto the surface. An attachment coefficient is adopted to describe the probability of successful foulant attachment for any given collision event, the value of which can be determined by the classical Boltzmann distribution. Our model shows excellent agreement with experimental data in terms of both the kinetics of flux decline and foulant mass deposition. Modeling results reveal the critical roles of water flux and energy barrier in governing colloidal fouling. Greater water flux or lower energy barrier can lead to a collision-controlled condition, where severe fouling occurs and nearly all collision events lead to successful foulant attachment. On the contrary, fouling is increasingly controlled by the probability of successful attachment at lower water flux and/or greater energy barrier. Our model provides deep insights into the various mechanisms governing the dynamics of colloidal fouling (i.e., concentration polarization, collision, and attachment) and the self-limiting fouling behavior under constant-pressure mode.
View details for PubMedID 29313680
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3D visualization of the internal nanostructure of polyamide thin films in RO membranes
JOURNAL OF MEMBRANE SCIENCE
2016; 501: 33-44
View details for DOI 10.1016/j.memsci.2015.10.061
View details for Web of Science ID 000368629100004
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Modeling and optimizing the performance of PVC/PVB ultrafiltration membranes using supervised learning approaches
RSC ADVANCES
2016; 6 (33): 28038-28046
View details for DOI 10.1039/c5ra24654g
View details for Web of Science ID 000372644100090
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Carbon-silica composite nanofiber membrane for high flux separation of water-in-oil emulsion - Performance study and fouling mechanism
SEPARATION AND PURIFICATION TECHNOLOGY
2015; 156: 952-960
View details for DOI 10.1016/j.seppur.2015.08.008
View details for Web of Science ID 000366538000007
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A Self-Assembled Superhydrophobic Electrospun Carbon-Silica Nanofiber Sponge for Selective Removal and Recovery of Oils and Organic Solvents
CHEMISTRY-A EUROPEAN JOURNAL
2015; 21 (14): 5395-5402
Abstract
An oil spill needs timely cleanup before it spreads and poses serious environmental threat to the polluted area. This always requires the cleanup techniques to be efficient and cost-effective. In this work, a lightweight and compressible sponge made of carbon-silica nanofibers is derived from electrospinning nanotechnology that is low-cost, versatile, and readily scalable. The fabricated sponge has high porosity (>99 %) and displays ultra-hydrophobicity and superoleophilicity, thus making it a suitable material as an oil adsorbent. Owing to its high porosity and low density, the sponge is capable of adsorbing oil up to 140 times its own weight with its sorption rate showing solution viscosity dependence. Furthermore, sponge regeneration and oil recovery are feasible by using either cyclic distillation or mechanical squeezing.
View details for DOI 10.1002/chem.201405670
View details for Web of Science ID 000352504500019
View details for PubMedID 25597480
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Effect of humic acid on the sorption of perfluorooctane sulfonate (PFOS) and perfluorobutane sulfonate (PFBS) on boehmite
CHEMOSPHERE
2015; 118: 213-218
Abstract
The sorption of PFOS and PFBS on boehmite was significantly retarded by the competitive sorption of humic acid (HA), implying that PFOS and PFBS are likely more mobile in water and groundwater systems enriched with HA. The sorption behavior of PFOS and PFBS on the HA-modified boehmite surface were also found to differ due to their different chain lengths. For a partially HA-modified boehmite surface, the isotherm study showed that PFOS had a much higher maximum sorption capacity than PFBS and that PFOS might possess additional surface interactions besides electrostatic interaction. For a HA-saturated boehmite, a linear sorption isotherm was found for PFOS while nearly no PFBS sorption was observed. This indicates that sorption behavior between PFOS and the sorbed HA on boehmite was dominated by hydrophobic interactions, instead of electrostatic interaction. In addition, a conceptual model combining hydrophobic and electrostatic interaction was established to explain the sorption behavior of PFOS and PFBS on HA-modified boehmite. Finally, the results revealed that the sorption of PFOS and PFBS on HA-modified boehmite is pH-dependent. The neutralization of negative sites on HA-modified boehmite reduced the electrostatic repulsion and enhanced the partitioning of PFBS on the sorbed HA.
View details for DOI 10.1016/j.chemosphere.2014.08.080
View details for Web of Science ID 000346953700030
View details for PubMedID 25268321
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Highly Efficient and Flexible Electrospun Carbon-Silica Nanofibrous Membrane for Ultrafast Gravity-Driven Oil-Water Separation
ACS APPLIED MATERIALS & INTERFACES
2014; 6 (12): 9393-9401
Abstract
A novel free-standing and flexible electrospun carbon-silica composite nanofibrous membrane is newly introduced. The characterization results suggest that the electrospun composite nanofibers are constructed by carbon chains interpenetrated through a linear network of 3-dimensional SiO2. Thermogravimetric analysis indicates that the presence of insulating silica further improve the thermal resistance of the membrane. Additionally, the mechanical strength test shows that the membrane's toughness and flexibility can be enhanced if the concentration of SiO2 is maintained below 2.7 wt %. Thermal and chemical stability test show that the membrane's wettability properties can be sustained at an elevated temperature up to 300 °C and no discernible change in wettability was observed under highly acidic and basic conditions. After surface-coating with silicone oil for 30 mins, the composite membrane exhibits ultra-hydrophobic and superoleophilic properties with water and oil contact angles being 144.2 ± 1.2° and 0°, respectively. The enhanced flexibility and selective wetting property enables the membrane to serve as an effective substrate for separating free oil from water. Lab-scale oil-water separation test indicates that the membrane possesses excellent oil-water separation efficiency. In addition, its inherent property of high porosity allows oil-water separation to be performed in a gravity-driven process with high-flux. We anticipate that this study will open up a new avenue for fabrication of free-standing carbonaceous composite membrane with tunable flexibility for energy efficient and high-throughput production of clean water.
View details for DOI 10.1021/am501758c
View details for Web of Science ID 000338184500058
View details for PubMedID 24867399
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Effects of inorganic anions on cadmium sorption behaviours on titanate nanotube surfaces
ENVIRONMENTAL TECHNOLOGY
2013; 34 (22): 3029-3033
View details for DOI 10.1080/09593330.2013.798035
View details for Web of Science ID 000327474200004
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Enterococcus spp on fomites and hands indicate increased risk of respiratory illness in child care centers
AMERICAN JOURNAL OF INFECTION CONTROL
2013; 41 (8): 728-733
Abstract
BACKGROUND: Surface-mediated transmission is a potential route for respiratory disease in child care centers, but evidence of its importance relative to other routes (eg, airborne) is limited. METHODS: We tracked respiratory disease and monitored bacteria contamination on hands and fomites over 4 months during 64 visits at 2 child care centers. Staff monitored health daily by recording respiratory symptoms. We measured concentrations of Escherichia coli, Enterococcus spp, and fecal coliform in hand rinses and on select fomites. RESULTS: We demonstrated that symptomatic respiratory illness was positively associated with microbial contamination on hands and fomites, as measured using Enterococcus spp. Enterococcus spp were 0.28 (95% confidence interval: 0.08-0.48)-log(10) (colony-forming units per 2 hands) higher when an individual had symptomatic respiratory illness. Susceptible individuals were 1.62 (95% confidence interval: 1.06-2.46) times more likely to develop respiratory illness within 4 days with every log(10) increase of Enterococcus spp on hands. CONCLUSION: The findings imply that hand contamination as measured using Enterococcus spp is a risk factor for onset of respiratory illness and highlight the utility of fecal indicator bacteria as a metric for hand and fomite contamination.
View details for DOI 10.1016/j.ajic.2012.10.013
View details for Web of Science ID 000322641100014
View details for PubMedID 23394857
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Critical Review of Desalination Concentrate Management, Treatment and Beneficial Use
ENVIRONMENTAL ENGINEERING SCIENCE
2013; 30 (8): 502-514
View details for DOI 10.1089/ees.2012.0348
View details for Web of Science ID 000323206400008
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Methodology to Capture Children's Non-Dietary Ingestion Exposure Activities During Meal Events
HUMAN AND ECOLOGICAL RISK ASSESSMENT
2013; 19 (4): 944-958
View details for DOI 10.1080/10807039.2012.702585
View details for Web of Science ID 000318592800009
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Effects of Chlorine Exposure Conditions on Physiochemical Properties and Performance of a Polyamide Membrane-Mechanisms and Implications
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2012; 46 (24): 13184-13192
View details for DOI 10.1021/es302867f
View details for Web of Science ID 000312432200021
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Effects of chlorine exposure conditions on physiochemical properties and performance of a polyamide membrane--mechanisms and implications.
Environmental science & technology
2012; 46 (24): 13184-13192
Abstract
Understanding the effects of chlorine exposure on polyamide (PA) based membranes is essential in membrane lifespan improvement. In this study, NF90 nanofiltration membrane was treated with sodium hypochlorite at different concentrations, pHs and durations. The changes in membrane elemental composition and bonding chemistry obtained from XPS and ATR-FTIR revealed the impacts of two competing mechanisms: N-chlorination and chlorination-promoted hydrolysis. More chlorine was incorporated into the PA matrix at pH <7, at which HOCl is dominant, while chlorine-promoted hydrolysis was more favorable at pH >7 with abundant hydroxyl groups. The membrane surface became more hydrophobic when chlorination was dominant, which in turn caused the water permeability of chlorinated membrane to decrease. Meanwhile, membrane became more hydrophilic and less cross-linked when hydrolysis effects were governing, which made the membrane more permeable for water. Rejection of charged solutes [NaCl, As(V)] improved in most chlorinating conditions due to increased charge density. However, when hydrolysis was severe (≥ 1000 ppm, pH 7 and 9), the enhanced charge repulsion effect could not compensate for the extensive amide bond cleavage, resulting in declined rejection. The lower rejection of neutral boric acid provided strong evidence of a less cross-linked separation layer.
View details for DOI 10.1021/es302867f
View details for PubMedID 23214945
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Effects of hypochlorous acid exposure on the rejection of salt, polyethylene glycols, boron and arsenic(V) by nanofiltration and reverse osmosis membranes
WATER RESEARCH
2012; 46 (16): 5217-5223
View details for DOI 10.1016/j.watres.2012.06.044
View details for Web of Science ID 000309095800030
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Effects of hypochlorous acid exposure on the rejection of salt, polyethylene glycols, boron and arsenic(V) by nanofiltration and reverse osmosis membranes.
Water research
2012; 46 (16): 5217-5223
Abstract
The separation layer of polyamide-based (PA) thin film composite (TFC) membranes can be modified by active chlorine species. The PA-TFC membranes, NF90, BW30 and NF270, were exposed to different concentrations of sodium hypochlorite (NaOCl) at pH 5 for 24 h. Elemental composition obtained from X-ray Photoelectron Spectroscopy (XPS) showed that the chlorine content in the PA layer increased with the chlorine concentrations. Treatment of membranes with 10 ppm Cl increased the membrane hydrophilicity. By contrast, when treated with 1000 ppm Cl or more, the membranes became less hydrophilic. Water permeability values for all 3 membrane types declined with increased chlorine concentrations. Filtration of polyethylene glycols (PEGs) with molecular weights of 200, 400 and 600 Daltons (Da) was performed to investigate the influence of chlorine treatment on membrane molecular weight cut off (MWCO) and rejection by size exclusion. Treatment with 10 and 100 ppm Cl lowered the MWCO while treatment with higher concentrations increased the MWCO. All chlorinated membranes experienced higher NaCl rejection compared to virgin ones. The performance of NF90 was tested with respect to the rejection of inorganic contaminants including boron (H(3)BO(3)) and arsenic (H(2)AsO(4)(-)). The boron rejection results paralleled PEG rejection whereas those for arsenic followed NaCl rejection patterns. The changes in membrane performance due to chlorine treatment were explained in terms of competing mechanisms: membrane tightening, bond cleavage by N-chlorination and chlorination promoted polyamide hydrolysis.
View details for DOI 10.1016/j.watres.2012.06.044
View details for PubMedID 22818949
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Adsorption of perfluorinated compounds on thin-film composite polyamide membranes
JOURNAL OF APPLIED POLYMER SCIENCE
2012; 124 (2): 1042-1049
View details for DOI 10.1002/app.35182
View details for Web of Science ID 000298672800019
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Degradation of Polyamide Nanofiltration and Reverse Osmosis Membranes by Hypochlorite
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2012; 46 (2): 852-859
Abstract
The degradation of polyamide (PA) nanofiltration and reverse osmosis membranes by chlorine needs to be understood in order to develop chlorine-resistant membranes. Coated and uncoated fully aromatic (FA) and piperazine (PIP) semi-aromatic PA membranes were treated with hypochlorite solution and analyzed by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR). XPS results showed that in chlorine treated FA PA membranes the ratio of bound chlorine to surface nitrogen was 1:1 whereas it was only 1:6 in the case of PIP PA membranes. Surface oxygen of uncoated FA and PIP membranes increased with increasing hypochlorite concentration whereas it decreased for coated FA membranes. High resolution XPS data support that chlorination increased the number of carboxylic groups on the PA surface, which appear to form by hydrolysis of the amide bonds (C(O)-N). FTIR data indicated the disappearance of the amide II band (1541 cm(-1)) and aromatic amide peak (1609 cm(-1)) in both coated and uncoated chlorinated FA membranes, consistent with the N-chlorination suggested by the XPS results. Furthermore, the surface charge of chlorinated membranes at low pH (<6) became negative, consistent with amide-nitrogen chlorination. Chlorination appeared to both increase and decrease membrane hydrophobicity depending on chlorination exposure conditions, which implied that N-chlorination and hydrolysis may be competing processes. The effects of property changes on the membrane performance were also observed for NF90, BW30, and NF270 membranes.
View details for DOI 10.1021/es203090y
View details for Web of Science ID 000299136200038
View details for PubMedID 22221176
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Quantified outdoor micro-activity data for children aged 7-12-years old
JOURNAL OF EXPOSURE SCIENCE AND ENVIRONMENTAL EPIDEMIOLOGY
2012; 22 (1): 82-92
Abstract
Estimation of aggregate exposure and risk requires detailed information regarding dermal contact and mouthing activity. We analyzed micro-level activity time series (MLATS) of children aged 7-12 years to quantify these contact behaviors and evaluate differences by age and gender. In all, 18 children, aged 7-12 years, were videotaped while playing outdoors. Video footage was transcribed via Virtual Timing Device (VTD) software. We calculated the hand and mouth contact frequency, hourly duration and median duration of contact with 16 object categories. Median mouthing frequencies were 12.6 events/h and 2.6 events/h for hands and non-dietary objects, respectively. Median hourly mouthing duration was 0.4 min/h and 0.1 min/h with hands and objects. Median mouthing contact duration was 1 s and 1.5 s with hands and objects, respectively. The median object contact frequency for both the hands combined was 537.3 events/h with an hourly contact duration of 81.8 min/h and a median contact duration of 3 s. There were no significant differences in the mouthing activity between genders or age groups. Female children had longer and more frequent hand contacts with several surface types. Age was negatively correlated with hand contacts of floor and wood surfaces. Contact frequencies in this study are higher than current regulatory recommendations for this age group.
View details for DOI 10.1038/jes.2011.34
View details for Web of Science ID 000298248200009
View details for PubMedID 21989500
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Relative Pesticide and Exposure Route Contribution to Aggregate and Cumulative Dose in Young Farmworker Children
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH
2012; 9 (1): 73-96
Abstract
The Child-Specific Aggregate Cumulative Human Exposure and Dose (CACHED) framework integrates micro-level activity time series with mechanistic exposure equations, environmental concentration distributions, and physiologically-based pharmacokinetic components to estimate exposure for multiple routes and chemicals. CACHED was utilized to quantify cumulative and aggregate exposure and dose estimates for a population of young farmworker children and to evaluate the model for chlorpyrifos and diazinon. Micro-activities of farmworker children collected concurrently with residential measurements of pesticides were used in the CACHED framework to simulate 115,000 exposure scenarios and quantify cumulative and aggregate exposure and dose estimates. Modeled metabolite urine concentrations were not statistically different than concentrations measured in the urine of children, indicating that CACHED can provide realistic biomarker estimates. Analysis of the relative contribution of exposure route and pesticide indicates that in general, chlorpyrifos non-dietary ingestion exposure accounts for the largest dose, confirming the importance of the micro-activity approach. The risk metrics computed from the 115,000 simulations, indicate that greater than 95% of these scenarios might pose a risk to children's health from aggregate chlorpyrifos exposure. The variability observed in the route and pesticide contributions to urine biomarker levels demonstrate the importance of accounting for aggregate and cumulative exposure in establishing pesticide residue tolerances in food.
View details for DOI 10.3390/ijerph9010073
View details for Web of Science ID 000299532000006
View details for PubMedID 22470279
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An Ontology-based Service Model For Smart Infrastructure Design
International Conference on Cloud Computing and Service Computing (CSC)
IEEE. 2012: 17–24
View details for DOI 10.1109/CSC.2012.11
View details for Web of Science ID 000314986700004
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Effect of bromide on the chlorination of a polyamide membrane
DESALINATION
2011; 280 (1-3): 80-86
View details for DOI 10.1016/j.desal.2011.06.046
View details for Web of Science ID 000296365800010
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Comparison of Surface Sampling Methods for Virus Recovery from Fomites
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
2011; 77 (19): 6918-6925
Abstract
The role of fomites in infectious disease transmission relative to other exposure routes is difficult to discern due, in part, to the lack of information on the level and distribution of virus contamination on surfaces. Comparisons of studies intending to fill this gap are difficult because multiple different sampling methods are employed and authors rarely report their method's lower limit of detection. In the present study, we compare a subset of sampling methods identified from a literature review to demonstrate that sampling method significantly influences study outcomes. We then compare a subset of methods identified from the review to determine the most efficient methods for recovering virus from surfaces in a laboratory trial using MS2 bacteriophage as a model virus. Recoveries of infective MS2 and MS2 RNA are determined using both a plaque assay and quantitative reverse transcription-PCR, respectively. We conclude that the method that most effectively recovers virus from nonporous fomites uses polyester-tipped swabs prewetted in either one-quarter-strength Ringer's solution or saline solution. This method recovers a median fraction for infective MS2 of 0.40 and for MS2 RNA of 0.07. Use of the proposed method for virus recovery in future fomite sampling studies would provide opportunities to compare findings across multiple studies.
View details for DOI 10.1128/AEM.05709-11
View details for Web of Science ID 000295123300023
View details for PubMedID 21821742
View details for PubMedCentralID PMC3187074
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Sequestration of cadmium ions using titanate nanotube
JOURNAL OF HAZARDOUS MATERIALS
2011; 187 (1-3): 401-406
Abstract
In this manuscript, titanate (Na(2)Ti(3)O(7)) nanotubes synthesized from alkali hydrothermal route, with high BET surface area (206 m(2)/g), were used as an effective sorbent to remove cadmium ions from water. Sorption capacity (q(m,Langmuir) = 1.1 mmol/g at pH 7) was higher than other sorbents. X-ray photoelectron spectroscopy (XPS) analyses performed on fresh and cadmium-sorbed samples reveal intensities of Na 1s peak decreased after sorption indicating ion-exchanging between cadmium and sodium ions occurred at interlayer of nanotubes. However kinetic study did not show a stoichiometrically equivalent amount of Na(+) being released suggesting Cd uptake was not due solely to ion-exchange mechanism. Batch tests also showed that cadmium uptake was not significantly affected by variation in ionic strength, signifying cadmium ions form an inner-sphere complexation with surface hydroxyl groups. Finally, surface complexation modeling was performed based on charge distribution multisite ion complexation (CDMUSIC) model. It was found that CDMUSIC was able to fit the experimental data best when inner-sphere complexation and ion-exchange were applied together.
View details for DOI 10.1016/j.jhazmat.2011.01.053
View details for Web of Science ID 000288630800049
View details for PubMedID 21295400
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Selective sorption of divalent cations using a high capacity sorbent
JOURNAL OF HAZARDOUS MATERIALS
2011; 187 (1-3): 96-100
Abstract
This manuscript describes the application of a novel sorbent, sodium titanate nanotube (STN) on partitioning of various divalent cations. Seven divalent cations, from alkaline earth, transition and post-transition groups, were used to determine the capacity and selectivity of STN. At pH 3 ± 0.02 and 0.1M ionic strength, STN displayed high capacity for Pb and Cd (1.27 and 0.39 mmol/g, correspondingly). The affinity of divalent cations was in the order Pb ≫ Cd>Cu>Zn>Ca>Sr>Ni. For six of the tested cations, their sorption capacity can be linearly correlated to its hydrolysis constant and electronegativity. STN has unusually low affinity for Ni and correlations of sorption capacity of Ni falls outside the 95% confidence intervals. Furthermore, it exhibited sorption behavior similar to alkaline earth cations, significant uptakes occurred only when pH>point of zero charge. In competitive sorption tests, STN preferentially sorb Cd over other metals (Zn, Ni, Ca and Sr) which coexist in industrial wastewater. As such STN is a potential novel sorbent useful for partitioning Cd from other metals in industrial wastewater.
View details for DOI 10.1016/j.jhazmat.2010.12.120
View details for Web of Science ID 000288630800011
View details for PubMedID 21295911
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Systematic study on calcium-alginate interaction in a hybrid coagulation-nanofiltration system
JOURNAL OF MEMBRANE SCIENCE
2011; 370 (1-2): 109-115
View details for DOI 10.1016/j.memsci.2010.12.047
View details for Web of Science ID 000288355400011
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A decision-support system for smarter city planning and management
IBM JOURNAL OF RESEARCH AND DEVELOPMENT
2011; 55 (1-2)
View details for DOI 10.1147/JRD.2010.2096572
View details for Web of Science ID 000301498300009
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Virus transfer between fingerpads and fomites
JOURNAL OF APPLIED MICROBIOLOGY
2010; 109 (6): 1868-1874
Abstract
Virus transfer between individuals and fomites is an important route of transmission for both gastrointestinal and respiratory illness. The present study examines how direction of transfer, virus species, time since last handwashing, gender, and titre affect viral transfer between fingerpads and glass.Six hundred fifty-six total transfer events, performed by 20 volunteers using MS2, φX174, and fr indicated 0·23 ± 0·22 (mean and standard deviation) of virus is readily transferred on contact. Virus transfer is significantly influenced by virus species and time since last handwashing. Transfer of fr bacteriophage is significantly higher than both MS2 and φX174. Virus transfer between surfaces is reduced for recently washed hands.Viruses are readily transferred between skin and surfaces on contact. The fraction of virus transferred is dependent on multiple factors including virus species, recently washing hands, and direction of transfer likely because of surface physicochemical interactions.The study is the first to provide a large data set of virus transfer events describing the central tendency and distribution of fraction virus transferred between fingers and glass. The data set from the study, along with the quantified effect sizes of the factors explored, inform studies examining role of fomites in disease transmission.
View details for DOI 10.1111/j.1365-2672.2010.04814.x
View details for Web of Science ID 000284170300002
View details for PubMedID 20659186
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Hybrid coagulation-nanofiltration membrane for removal of bromate and humic acid in water
JOURNAL OF MEMBRANE SCIENCE
2010; 365 (1-2): 154-159
View details for DOI 10.1016/j.memsci.2010.08.048
View details for Web of Science ID 000284750300018
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Formation of copper aluminate spinel and cuprous aluminate delafossite to thermally stabilize simulated copper-laden sludge
JOURNAL OF HAZARDOUS MATERIALS
2010; 181 (1-3): 399-404
Abstract
The study reported herein indicated the stabilization mechanisms at work when copper-laden sludge is thermally treated with gamma-alumina and kaolinite precursors, and evaluated the prolonged leachability of their product phases. Four copper-containing phases - copper oxide (CuO), cuprous oxide (Cu(2)O), copper aluminate spinel (CuAl(2)O(4)), and cuprous aluminate delafossite (CuAlO(2)) - were found in the thermal reactions of the investigated systems. These phases were independently synthesized for leaching by 0.1M HCl aqueous solution, and the relative leachabilities were found to be CuAl(2)O(4)
View details for DOI 10.1016/j.jhazmat.2010.05.024
View details for Web of Science ID 000280601300051
View details for PubMedID 20570043
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Characterization of isolated polyamide thin films of RO and NF membranes using novel TEM techniques
JOURNAL OF MEMBRANE SCIENCE
2010; 358 (1-2): 51-59
View details for DOI 10.1016/j.memsci.2010.04.032
View details for Web of Science ID 000279277400007
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Effect of solution chemistry on the adsorption of perfluorooctane sulfonate onto mineral surfaces
WATER RESEARCH
2010; 44 (8): 2654-2662
View details for DOI 10.1016/j.watres.2010.01.038
View details for Web of Science ID 000277556300026
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Effect of solution chemistry on the adsorption of perfluorooctane sulfonate onto mineral surfaces.
Water research
2010; 44 (8): 2654-2662
Abstract
Perfluorooctane sulfonate (PFOS) is an emergent contaminant of substantial environmental concerns, yet very limited information has been available on PFOS adsorption onto mineral surfaces. PFOS adsorption onto goethite and silica was investigated by batch adsorption experiments under various solution compositions. Adsorption onto silica was only marginally affected by pH, ionic strength, and calcium concentration, likely due to the dominance of non-electrostatic interactions. In contrast, PFOS uptake by goethite increased significantly at high [H+] and [Ca2+], which was likely due to enhanced electrostatic attraction between the negatively charged PFOS molecules and positively charged goethite surface. The effect of pH was less significant at high ionic strength, likely due to electrical double layer compression. PFOS uptake was reduced at higher ionic strength for a strongly positively charged goethite surface (pH 3), while it increased for a weakly charged surface (pH 7 and 9), which could be attributed to the competition between PFOS-surface electrostatic attraction and PFOS-PFOS electrostatic repulsion. A conceptual model that captures PFOS-surface and PFOS-PFOS electrostatic interactions as well as non-electrostatic interaction was also formulated to understand the effect of solution chemistry on PFOS adsorption onto goethite and silica surfaces.
View details for DOI 10.1016/j.watres.2010.01.038
View details for PubMedID 20172580
- Effect of solution chemistry on the adsorption of perfluorooctanesulfonate onto mineral surfaces Water Research 2010; 8 (44): 2654 – 2662
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Fouling mechanism and resistance analyses of systems containing sodium alginate, calcium, alum and their combination in dead-end fouling of nanofiltration membranes
JOURNAL OF MEMBRANE SCIENCE
2009; 344 (1-2): 244-251
View details for DOI 10.1016/j.memsci.2009.08.010
View details for Web of Science ID 000270694200031
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Farmworker children's residential non-dietary exposure estimates from micro-level activity time series
ENVIRONMENT INTERNATIONAL
2009; 35 (8): 1202-1209
Abstract
Farmworkers' children may have increased pesticide exposure through dermal absorption and non-dietary ingestion, routes that are difficult to measure and model. The Cumulative Aggregate Simulation of Exposure (CASE) model, integrates the complexity of human behavior and variability of exposure processes by combining micro-level activity time series (MLATS) and mechanistic exposure equations. CASE was used to estimate residential non-dietary organophosphate pesticide exposure (i.e., inhalation, dermal, and non-dietary ingestion) to California farmworker children and evaluate the micro-activity approach. MLATS collected from children and distributions developed from pesticide measurements in farmworkers' residences served as inputs. While estimated diazinon exposure was greater for inhalation, chlorpyrifos exposure was greater for the other routes. Greater variability existed between children (sigma(B)(2)=0.22-0.39) than within each child's simulations (sigma(W)(2)=0.01-0.02) for dermal and non-dietary ingestion. Dermal exposure simulations were not significantly different than measured values from dosimeters worn by the children. Non-dietary ingestion exposure estimates were comparable to duplicate diet measurements, indicating this route may contribute substantially to aggregate exposure. The results suggest the importance of the micro-activity approach for estimating non-dietary exposure. Other methods may underestimate exposure via these routes. Model simulations can be used to identify at-risk children and target intervention strategies.
View details for DOI 10.1016/j.envint.2009.08.003
View details for Web of Science ID 000271360900014
View details for PubMedID 19744713
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Influence of a prolonged solid retention time environment on nitrification/denitrification and sludge production in a submerged membrane bioreactor
DESALINATION
2009; 245 (1-3): 28-43
View details for DOI 10.1016/j.desal.2008.06.010
View details for Web of Science ID 000269141300003
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Effect of membrane chemistry and coating layer on physiochemical properties of thin film composite polyamide RO and NF membranes II. Membrane physiochemical properties and their dependence on polyamide and coating layers
DESALINATION
2009; 242 (1-3): 168-182
View details for DOI 10.1016/j.desal.2008.04.004
View details for Web of Science ID 000266152500014
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Effect of membrane chemistry and coating layer on physiochemical properties of thin film composite polyamide RO and NF membranes I. FTIR and XPS characterization of polyamide and coating layer chemistry
DESALINATION
2009; 242 (1-3): 149-167
View details for DOI 10.1016/j.desal.2008.04.003
View details for Web of Science ID 000266152500013
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Fabrication and photocatalytic activity of porous TiO2 nanowire microspheres by surfactant-mediated spray drying process
MATERIALS RESEARCH BULLETIN
2009; 44 (5): 1070-1076
View details for DOI 10.1016/j.materresbull.2008.10.017
View details for Web of Science ID 000264969200021
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A Model of Exposure to Rotavirus from Nondietary Ingestion Iterated by Simulated Intermittent Contacts
RISK ANALYSIS
2009; 29 (5): 617-632
Abstract
Existing microbial risk assessment models rarely incorporate detailed descriptions of human interaction with fomites. We develop a stochastic-mechanistic model of exposure to rotavirus from nondietary ingestion iterated by simulated intermittent fomes-mouth, hand-mouth, and hand-fomes contacts typical of a child under six years of age. This exposure is subsequently translated to risk using a simple static dose-response relationship. Through laboratory experiments, we quantified the mean rate of inactivation for MS2 phage on glass (0.0052/hr) and mean transfer between fingertips and glass (36%). Simulations using these parameters demonstrated that a child's ingested dose from a rotavirus-contaminated ball ranges from 2 to 1,000 virus over a period of one hour, with a median value of 42 virus. These results were heavily influenced by selected values of model parameters, most notably the concentration of rotavirus on fomes, frequency of fomes-mouth contacts, frequency of hand-mouth contacts, and virus transferred from fomes to mouth. The model demonstrated that mouthing of fomes is the primary exposure route, with hand mouthing contributions accounting for less than one-fifth of the child's dose over the first 10 minutes of interaction.
View details for DOI 10.1111/j.1539-6924.2008.01193.x
View details for Web of Science ID 000264892100002
View details for PubMedID 19187484
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Organic fouling of nanofiltration membranes: Evaluating the effects of humic acid, calcium, alum coagulant and their combinations on the specific cake resistance
JOURNAL OF MEMBRANE SCIENCE
2009; 332 (1-2): 56-62
View details for DOI 10.1016/j.memsci.2009.01.037
View details for Web of Science ID 000265313600008
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Developing probability distributions for transfer efficiencies for dermal exposure
JOURNAL OF EXPOSURE SCIENCE AND ENVIRONMENTAL EPIDEMIOLOGY
2009; 19 (3): 274-283
Abstract
Many dermal exposure models use stochastic techniques to sample parameter distributions derived from experimental data to more accurately represent variability and uncertainty. Transfer efficiencies represent the fraction of a surface contaminant transferred from the surface to the skin during a contact event. Although an important parameter for assessing dermal exposure, examination of the literature confirms that no single study is large enough to provide a basis for a transfer efficiency distribution for use in stochastic dermal exposure models. It is therefore necessary to combine data sets from multiple studies to achieve the largest data set possible for distribution analysis. A literature review was conducted to identify publications reporting transfer efficiencies. Data sets were compared using the Kruskal-Wallis test to determine whether they arise from the same distribution. Combined data were evaluated for several theoretical distributions using the Kolmogorov-Smirnov and chi(2)-goodness-of-fit tests. Our literature review identified 35 studies comprising 25 different sampling methods, 25 chemicals, and 10 surface types. Distributions were developed for three different chemicals (chlorpyrifos, pyrethrin I, and piperonyl butoxide) on three different surface types (carpet, vinyl, and foil). Only the lognormal distribution was consistently accepted for each chemical and surface combination. Fitted distributions were significantly different (Kruskal-Wallis test; P<0.001) across chemicals and surface types. In future studies, increased effort should be placed on developing large studies, which more accurately represent transfer to human skin from surfaces, and on developing a normative transfer efficiency measure so that data from different methodologies can be compared.
View details for DOI 10.1038/jes.2008.16
View details for Web of Science ID 000263457600004
View details for PubMedID 18385671
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Combination of one-dimensional TiO2 nanowire photocatalytic oxidation with microfiltration for water treatment
WATER RESEARCH
2009; 43 (5): 1179-1186
Abstract
This paper proposed the fabrication of two different diameter one-dimensional TiO2 nanowires, 10 nm TNW10 and 20-100 nm TNW20, via hydrothermal process using different alkaline sources. TNW10 and TNW20 were used as photocatalysts for the degradation of humic acid (HA), the major natural organic matters (NOMs) in surface and ground water, followed by microfiltration. The evaluation of photocatalytic activities of them showed that TNW10 was superior to the commercial P25 TiO2 while TNW20 was as good as P25. The membrane filtration verified that the two types of nanowires could be completely reclaimed. The membrane fouling caused by TNW10 and TNW20 was much less than that of P25 due to more porous cake and less pore plugging. No apparent decrease on their photocatalytic activity was observed in repeated reuse experiments. These one-dimensional TiO2 nanowires would provide a new route for the combination of photocatalytic oxidation and membrane filtration for water treatment.
View details for DOI 10.1016/j.watres.2008.12.021
View details for Web of Science ID 000264616300003
View details for PubMedID 19157486
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The role of foulant-foulant electrostatic interaction on limiting flux for RO and NF membranes during humic acid fouling-Theoretical basis, experimental evidence, and AFM interaction force measurement
JOURNAL OF MEMBRANE SCIENCE
2009; 326 (2): 526-532
View details for DOI 10.1016/j.memsci.2008.10.043
View details for Web of Science ID 000263006500033
- A Model of Exposure to Rotavirus from Non-Dietary Ingestion Iterated by Simulated Intermittent Contacts Risk Analysis 2009; 5 (29): 617-632
- Effect of membrane chemistry and coating layer on physiochemical properties of thin film composite polyamide RO and NF membranes. II. Membrane physiochemical properties and their dependence on polyamide and coating layers Desalination 2009; 1-3 (242): 168 – 182
- Fabrication and photocatalytic activity of porous TiO nanowire microspheres by surfactant-mediated spray drying process Materials Research Bulletin 2009; 5 (44): 1070 - 1076
- Effect of membrane chemistry and coating layer on physiochemical properties of thin film composite polyamide RO and NF membranes. I. FTIR and XPS characterization of polyamide and coating layer chemistry Desalination 2009; 1-3 (242): 149 – 167
- Combination of one-dimensional TiO nanowire photocatalytic oxidation with microfiltration for water treatment Water Research 2009; 5 (43): 1179 – 1186
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The fraction of total hand surface area involved in young children's outdoor hand-to-object contacts
ENVIRONMENTAL RESEARCH
2008; 108 (3): 294-299
Abstract
Information on the fraction of total hand surface area touching a contaminated object is necessary in accurately estimating contaminant (e.g., pesticides, pathogens) loadings onto the hands during hand-to-object contacts. While several existing physical-stochastic human exposure models require such surface area data to estimate dermal and non-dietary ingestion exposure, there are very limited data sets. This paper provides statistical distributions of fractional surface areas (FSAs) for children's outdoor hand contacts. These distributions were constructed by combining information collected from two distinct studies exploring children's activity patterns and quantifying hand contact surface area. Results show that for outdoor contacts with "All Objects", a range of 0.13-0.27 captured median FSAs, while a range of 0.12-0.24 captured time-weighted FSAs. Overall, an FSA of 0.31 captured 80-100% of FSAs involved in each child's outdoor hand contacts, depending upon the object of interest. These values are much lower than the often conservative assumptions of up to 1 (i.e., the entire hand) that researchers currently make regarding FSAs involved in indoor and outdoor contacts [USEPA, 1997. Standard operating procedures (SOPs) for residential exposure assessments. Contract no. 68-W6-0030. http://www.epa.gov/pesticides/trac/science/trac6a05.pdf].
View details for DOI 10.1016/j.envres.2008.07.010
View details for Web of Science ID 000260660000004
View details for PubMedID 18760778
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Grafted multifunctional titanium dioxide nanotube membrane: Separation and photodegradation of aquatic pollutant
APPLIED CATALYSIS B-ENVIRONMENTAL
2008; 84 (1-2): 262-267
View details for DOI 10.1016/j.apcatb.2008.04.009
View details for Web of Science ID 000260728300033
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Quantified activity pattern data from 6 to 27-month-old farmworker children for use in exposure assessment
ENVIRONMENTAL RESEARCH
2008; 108 (2): 239-246
Abstract
This study was conducted to describe exposure prone behaviors of infants and toddlers in the farmworker community. Analysis of hand and mouth contact frequencies and durations aids understanding of how children interact with their environment and are exposed via contact with surfaces. All 23 participating children (8 female infants, 5 male infants, 5 female toddlers and 5 male toddlers) lived with at least one farmworker. Children were videotaped at home for 2-6 h. Video footage was translated into micro-level activity time series (MLATS) for both hands and the mouth. MLATS were processed to calculate hourly duration in microenvironments, contact frequency, hourly contact duration and median contact duration. The median hourly duration spent indoors was 53 min/h. The median hand-to-mouth frequency was 15.2 events/h and the median object-to-mouth frequency was 27.2 events/h. The hourly mouthing duration was 1.2 and 2.2 min/h with the hands and objects, respectively. The median mouthing duration with hands and objects was 2 s. The median contact frequency for both hands combined was 689.4 events/h with an hourly contact duration of 100.5 min/h and a median contact duration of 3s. Infants had higher mouthing frequencies with non-dietary objects while toddlers had higher mouthing frequencies with objects associated with pica (i.e., paper). Boys had higher contact frequencies while girls had longer contact durations. These sub-group differences indicate factors such as age and gender should be accounted for when conducting exposure assessments. Contact frequencies in this study are higher than current US EPA recommendations, questioning their protective value for infants and toddlers.
View details for DOI 10.1016/j.envres.2008.07.007
View details for Web of Science ID 000260132400015
View details for PubMedID 18723168
View details for PubMedCentralID PMC2613792
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Self-etching reconstruction of hierarchically mesoporous F-TiO2 hollow microspherical photocatalyst for concurrent membrane water Purifications
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2008; 130 (34): 11256-?
Abstract
We report a large-scale self-etching approach for the synthesis of monodispersed mesoporous F-TiO2 hollow microspheres. The self-etching derived from HF was elucidated by the morphology, chemical composition, and crystal size evolutions from solid to hollow microspheres with the increase in the concentration of H2SO4. The resulting TiO2 hollow microspheres exhibited ease for the concurrent membrane filtration and photocatalysis, providing high potential for engineering application in advanced water treatment, for not only increasing water production but also improving water quality.
View details for DOI 10.1021/ja803582m
View details for Web of Science ID 000258660600007
View details for PubMedID 18680296
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Synthesis of bimodal porous structured TiO2 microsphere with high photocatalytic activity for water treatment
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
2008; 324 (1-3): 202-207
View details for DOI 10.1016/j.colsurfa.2008.04.015
View details for Web of Science ID 000257908600034
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Change of chemical composition and hydrogen bonding behavior due to chlorination of crosslinked polyamide membranes
JOURNAL OF APPLIED POLYMER SCIENCE
2008; 108 (4): 2061-2066
View details for DOI 10.1002/app.25657
View details for Web of Science ID 000254672800001
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Palladium-indium catalyzed reduction of N-nitrosodimethylamine: Indium as a promoter metal
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2008; 42 (8): 3040-3046
Abstract
An emerging technology for the removal of N-nitrosodimethylamine (NDMA) from drinking and groundwater is reductive destruction using noble metal catalysts and hydrogen gas as a reducing agent. Bimetallic palladium-indium (Pd-In) supported on alumina combines the ability of Into activate NDMA with the hydrogen activating properties of Pd. This study examined the effect of In addition to a commercial 5% Pd by weight on gamma-Al2O3 catalyst on the efficacy of NDMA reduction. The pseudo-first-order rate constant increased proportionately to In loading from 0.057 h(-1) for 0% In to a maximum of 0.25 h(-1) for 1% In and then decreased with additional in loading. Data suggest that hydrogen activation occurred only on Pd surfaces and In activated NDMA 20 times more effectively than Pd on a mass basis. The rate-limiting factor was NDMA activation for In loadings below 1%. The decrease at higher loadings is interpreted as In blocking pore spaces and limiting access to Pd sites, suggesting monatomic hydrogen limitation. The only products detected were dimethylamine and ammonium with carbon and nitrogen balances in excess of 92%, consistent with a mechanism involving reductive N-N bond cleavage. Results from this study serve as a basis for optimizing bimetallic catalysts for treating NDMA contaminated waters.
View details for DOI 10.1021/es7023115
View details for Web of Science ID 000254890400059
View details for PubMedID 18497163
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TiO2 nanowire membrane for concurrent filtration and photocatalytic oxidation of humic acid in water
JOURNAL OF MEMBRANE SCIENCE
2008; 313 (1-2): 44-51
View details for DOI 10.1016/j.memsci.2007.12.045
View details for Web of Science ID 000255208900004
- TiO nanowire membrane for concurrent filtration and photocatalytic oxidation of humic acid in water Journal of Membrane Science 2008; 1-2 (313): 44 – 51
- Aggregating TiO (B) nanowires to porous basketry-like microspheres and their photocatalytic properties Chemistry Letters 2008; 4 (37): 424 – 425
- Synthesis of bimodal porous structured TiO microsphere with high photocatalytic activity for water treatment Colloids and Surfaces A: Physicochemical and Engineering Aspects 2008; 1-3 (324): 202 - 207
- Self-etching reconstruction of hierarchically mesoporous F-TiO hollow microsphericalphotocatalyst for concurrent membrane water purifications Journal of the American Chemical Society 2008; 34 (130): 11256 – 11257
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Biofouling development and rejection enhancement in long SRT MF membrane bioreactor
PROCESS BIOCHEMISTRY
2007; 42 (12): 1641-1648
View details for DOI 10.1016/j.procbio.2007.09.009
View details for Web of Science ID 000252289400011
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Application of a stochastic model to estimate children's short-term residential exposure to lead
STOCHASTIC ENVIRONMENTAL RESEARCH AND RISK ASSESSMENT
2007; 21 (6): 737-745
View details for DOI 10.1007/s00477-006-0086-x
View details for Web of Science ID 000249579300008
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The influence of cobalt doping on photocatalytic nano-titania: Crystal chemistry and amorphicity
JOURNAL OF SOLID STATE CHEMISTRY
2007; 180 (10): 2905-2915
View details for DOI 10.1016/j.jssc.2007.08.021
View details for Web of Science ID 000251462100034
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Photocatalytic oxidation of pharmaceutical compounds: Kinetics and pathways for ibuprofen, clofibric acid, diclofenac and naproxen
JOURNAL OF ADVANCED OXIDATION TECHNOLOGIES
2007; 10 (2): 342-348
View details for Web of Science ID 000248358400018
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Membrane independent limiting flux for RO and NF membranes fouled by humic acid
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2007; 41 (13): 4767-4773
Abstract
The flux decline of reverse osmosis and nanofiltration membranes was investigated under constant pressure conditions during humic acid fouling tests. For a given membrane type under a given feedwater composition, increasing pressure resulted in increased flux reduction and foulant accumulation. A limiting flux seems to exist beyond which the membrane flux cannot be sustained. Membranes with initial fluxes greater than the limiting flux experienced severe fouling and their pseudo stable fluxes approached the limiting flux. Flux reduction was much milder when the initial flux was lower than the limiting flux. Furthermore, the limiting flux seems to be independent of membrane properties, probably due to the dominance of foulant--deposited-foulant interaction upon complete foulant coverage over membrane surfaces. On the other hand, strong dependence of the limiting flux on the feedwater composition was observed. The limiting flux was reduced at higher proton, calcium, and/or background electrolytes concentrations, likely due to reduced electrostatic repulsion under these conditions.
View details for DOI 10.1021/es063105w
View details for Web of Science ID 000247782500051
View details for PubMedID 17695927
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Impact of prolonged sludge retention time on the performance of a submerged membrane bioreactor
DESALINATION
2007; 208 (1-3): 101-112
View details for DOI 10.1016/j.desal.2006.04.076
View details for Web of Science ID 000246322700010
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An efficient bicomponent TiO2/SnO2 nanofiber photocatalyst fabricated by electrospinning with a side-by-side dual spinneret method
NANO LETTERS
2007; 7 (4): 1081-1085
Abstract
In this communication, we demonstrate that the electrospinning process with a side-by-side dual spinneret can be a simple approach for fabricating bicomponent TiO2/SnO2 nanofibers with controllable heterojunctions. Specifically, both of the TiO2 and SnO2 components in the nanofibers are fully exposed to the surface. This morphology fully utilized the photogenerated holes and electrons during the photocatalytic process, thus leading to a high photocatalytic activity. We believe that this versatile approach can be extended to fabricate other novel high-efficiency bicomponent photocatalysts.
View details for DOI 10.1021/nl061898e
View details for Web of Science ID 000245600500043
View details for PubMedID 17425281
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Effect of flux (transmembrane pressure) and membrane properties on fouling and rejection of reverse osmosis and nanofiltration membranes treating perfluorooctane sulfonate containing wastewater
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2007; 41 (6): 2008-2014
Abstract
Perfluorooctane sulfonate (PFOS) is an emergent contaminant of substantial environmental concerns. In this study, reverse osmosis (RO) and nanofiltration (NF) membranes were used to remove this toxic and persistent compound from PFOS-containing wastewater. Five RO membranes and three NF membranes were tested at a feed concentration of 10 ppm PFOS over 4 days, and the PFOS rejection and permeate flux performances were systematically investigated. PFOS rejection was well correlated to sodium chloride rejection. The rejection efficiencies for the RO membranes were > 99%, and those for the NF membranes ranged from 90-99%. Improvement in PFOS rejection, together with mild flux reduction (< 16%), was observed at longer filtration time. Such shifts in rejection and flux performance were probably due to the increased PFOS accumulation at longer duration, as shown by X-ray photoelectron spectroscopy and liquid chromatograph and tandem mass spectrometry results. A fraction of PFOS molecules might be entrapped in the polyamide layer of the composite membranes, which hindered the further passage of both water and other PFOS molecules. In a similar fashion, PFOS rejection and fouling were enhanced for greater initial flux and/or applied pressure, where PFOS accumulation was promoted probably due to increased hydrodynamic permeate drag. Flux reduction was also shown to correlate to membrane roughness, with the rougher membranes tend to experience more flux reduction than the smoother ones.
View details for DOI 10.1021/es062052f
View details for Web of Science ID 000244855100039
View details for PubMedID 17410798
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Fouling of reverse osmosis and nanofiltration membranes by humic acid - Effects of solution composition and hydrodynamic conditions
JOURNAL OF MEMBRANE SCIENCE
2007; 290 (1-2): 86-94
View details for DOI 10.1016/j.memsci.2006.12.017
View details for Web of Science ID 000244830000010
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Characterization of humic acid fouled reverse osmosis and nanofiltration membranes by transmission electron microscopy and streaming potential measurements
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2007; 41 (3): 942-949
Abstract
Reverse osmosis and nanofiltration membranes fouled by humic acid were systematically characterized by transmission electron microscopy. All fouled membranes, except those with very low initial flux, were completely covered by a layer of humic acid whose thickness and density were greatly affected by the feedwater composition ([H+] and [Ca2+]) and initial flux. A low-density humic layer (about 0.1 g of purified Aldrich humic acid (PAHA)/cm3) was formed at low initial flux (2 m/day or less) at pH 7 without calcium. It was several times denser at a higher initial flux, pH 4.5, or 1 mM Ca2+. Corresponding to the denser foulant layers under these conditions, PAHA accumulation was greatly increased. The denser foulant layers together with the greater PAHA accumulations were responsible for the severe flux reductions. Both virgin and fouled membranes were characterized by streaming potential measurements. While considerable differences existed for virgin membranes, humic acid fouled membranes exhibited identical surface charge properties. The zeta potential of the fouled membranes was controlled by the humic acid layer due to its complete coverage of the membrane surfaces.
View details for DOI 10.1021/es061322r
View details for Web of Science ID 000244002800051
View details for PubMedID 17328207
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Adsorption and photodegradation of humic acids by nano-structured TiO2 for water treatment
10th International Conference on Photocatalysis/11th International Conference on Advanced Oxidation Technologies for Treatment of Water, Air and Soil
SCIENCE & TECHNOLOGY NETWORK INC. 2007: 72–78
View details for Web of Science ID 000243772500012
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Probing the nano- and micro-scales of reverse osmosis membranes - A comprehensive characterization of physiochemical properties of uncoated and coated membranes by XPS, TEM, ATR-FTIR, and streaming potential measurements
JOURNAL OF MEMBRANE SCIENCE
2007; 287 (1): 146-156
View details for DOI 10.1016/j.memsci.2006.10.038
View details for Web of Science ID 000243621700019
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One-step fabrication and high photocatalytic activity of porous TiO2 hollow aggregates by using a low-temperature hydrothermal method without templates
CHEMISTRY-A EUROPEAN JOURNAL
2007; 13 (6): 1851-1855
Abstract
Porous TiO2 hollow aggregates have been synthesized on a large scale by means of a simple hydrothermal method without using any templates. The as-prepared products were characterized by means of field emission scanning electron microscopy, XRD, TEM, nitrogen adsorption, UV/Vis diffuse reflectance spectroscopy, and FTIR spectroscopy. The photocatalytic activity of the aggregates was demonstrated through the photocatalytic degradation of Rhodamine B. Structural characterization indicates that the porous TiO2 aggregates are 500-800 nm in diameter and display mesoporous structure. The average pore sizes and BET surface areas of the aggregates are 12 nm and 168 m2 g-1, respectively. Optical adsorption investigations show that the aggregates possess an optical band-gap energy of 3.36 eV. The as-prepared products were substantially more effective photocatalysts than the commercially available photocatalyst P25. The dye degradation rate of the porous TiO2 hollow aggregates is more than twice that of P25. The high photoactivities of the aggregates can be attributed to the combined effects of several factors, namely, large surface areas, the existence of mesopores, and the high band-gap energy. In addition, the as-prepared products can be easily recycled.
View details for DOI 10.1002/chem.200601092
View details for Web of Science ID 000244577400021
View details for PubMedID 17133639
- An efficient bicomponentTiO/SnOnanofiberphotocatalyst fabricated by electrospinning with a side-by-side dual spinneret method Nano Letters 2007; 4 (7): 1081 – 1085
- Fouling of reverse osmosis and nanofiltration membranes by humic acid-Effects of solution composition and hydrodynamic conditions Journal of Membrane Science 2007; 1-2 (290): 86 – 94
- Probing the nano- and micro-scales of reverse osmosis membranes-A comprehensive characterization of physiochemical properties of uncoated and coated membranes by XPS, TEM, ATR-FTIR, and streaming potential measurements Journal of Membrane Science 2007; 1 (287): 146 – 156
- Effect of flux (transmembrane pressure) and membrane properties on fouling and rejection of reverse osmosis and nanofiltration membranes treating perfluorooctanesulfonate containing wastewater Environmental Science & Technology 2007; 6 (41): 2008 - 2014
- The Influence of Cobalt-doping on PhotocatalyticNano-titania: Crystal Chemistry and Amorphicity Journal of Solid State Chemistry 2007; 10 (180): 2905-2915
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Nickel aluminate spinel formation during sintering of simulated Ni-laden sludge and kaolinite
JOURNAL OF THE EUROPEAN CERAMIC SOCIETY
2007; 27 (1): 91-99
View details for DOI 10.1016/j.jeurceramsoc.2006.04.176
View details for Web of Science ID 000242565400013
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Change of membrane performance due to chlorination of crosslinked polyamide membranes
JOURNAL OF APPLIED POLYMER SCIENCE
2006; 102 (6): 5895-5902
View details for DOI 10.1002/app.25071
View details for Web of Science ID 000241593800101
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Use of reverse osmosis membranes to remove perfluorooctane sulfonate (PFOS) from semiconductor wastewater
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2006; 40 (23): 7343-7349
Abstract
Perfluorooctane sulfonate (PFOS) and related substances are persistent, bioaccumulative, and toxic, and thus of substantial environmental concern. PFOS is an essential photolithographic chemical in the semiconductor industry with no substitutes yet identified. The industry seeks effective treatment technologies. The feasibility of using reverse osmosis (RO) membranes for treating semiconductor wastewater containing PFOS has been investigated. Commercial RO membranes were characterized in terms of permeability, salt rejection, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and membrane surface zeta potential (streaming potential measurements). Filtration tests were performed to determine the membrane flux and PFOS rejection. Over a wide range of feed concentrations (0.5 - 1500 ppm), the RO membranes generally rejected 99% or more of the PFOS. Rejection was better for tighter membranes, but was not affected by membrane zeta potential. Flux decreased with increasing PFOS concentration. While the flux reduction was severe for a loose RO membrane probably due to its higher initial flux, very stable flux was maintained for tighter membranes. At a very high feed concentration (about 500 ppm), all the membranes exhibited an identical stable flux. Isopropyl alcohol, present in some semiconductor wastewaters, had a detrimental effect on membrane flux. Where present it needs to be removed from the wastewater prior to using RO membranes.
View details for DOI 10.1021/es060831q
View details for Web of Science ID 000242367100040
View details for PubMedID 17180987
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Hypochlorite degradation of crosslinked polyamide membranes I. Changes in chemical/morphological properties
JOURNAL OF MEMBRANE SCIENCE
2006; 283 (1-2): 21-26
View details for DOI 10.1016/j.memsci.2006.06.008
View details for Web of Science ID 000240844900005
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Hypochlorite degradation of crosslinked polyamide membranes - II. Changes in hydrogen bonding behavior and performance
JOURNAL OF MEMBRANE SCIENCE
2006; 282 (1-2): 456-464
View details for DOI 10.1016/j.memsci.2006.06.004
View details for Web of Science ID 000240579700051
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Nickel stabilization efficiency of aluminate and ferrite spinels and their leaching behavior
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2006; 40 (17): 5520-5526
Abstract
Stabilization efficiencies of spinel-based construction ceramics incorporating simulated nickel-laden waste sludge were evaluated and the leaching behavior of products investigated. To simulate the process of immobilization, nickel oxide was mixed alternatively with gamma-alumina, kaolinite, and hematite. These tailoring precursors are commonly used to prepare construction ceramics in the building industry. After sintering from 600 to 1480 degrees C at 3 h, the nickel aluminate spinel (NiAl204) and the nickel ferrite spinel (NiFe204) crystallized with the ferrite spinel formation commencing about 200-300 degrees C lower than for the aluminate spinel. All the precursors showed high nickel incorporation efficiencies when sintered at temperatures greater than 1250 degrees C. Prolonged leach tests (up to 26 days) of product phases were carried out using a pH 2.9 acetic acid solution, and the spinel products were invariably superior to nickel oxide for immobilization over longer leaching periods. The leaching behavior of NiAl2O4 was consistent with congruent dissolution without significant reprecipitation, but for NiFe2O4, ferric hydroxide precipitation was evident. The major leaching reaction of sintered kaolinite-based products was the dissolution of cristobalite rather than NiAl2O4. This study demonstrated the feasibility of transforming nickel-laden sludge into spinel phases with the use of readily available and inexpensive ceramic raw materials, and the successful reduction of metal mobility under acidic environments.
View details for DOI 10.1021/es0601033
View details for Web of Science ID 000240130200058
View details for PubMedID 16999134
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Young children's hand contact activities: An observational study via videotaping in primarily outdoor residential settings
JOURNAL OF EXPOSURE SCIENCE AND ENVIRONMENTAL EPIDEMIOLOGY
2006; 16 (5): 434-446
Abstract
Microlevel activity time series (MLATS) data were gathered on hand contact activities of 38 children (1-6 years old) by videotaping in primarily outdoor residential environments. The videotape recordings were then translated into text files using a specialized software called VirtualTimingDevicetrade mark. Contact frequency (contacts/h), duration per contact (s/contact), and hourly contact duration (min/h) were summarized for outdoor hand contacts with 15 distinct object/surface categories ("Animal", "Body", "Clothes/Towels", "Fabric", "Floor", "Food", "Footwear", "Metal", "Non-dietary Water", "Paper/Wrapper", "Plastic", "Rock/Brick", "Toys", "Vegetation/Grass", and "Wood") and two aggregate object/surface categories ("Non-dietary objects/surfaces" and "Total objects/surfaces"). For outdoor both hand contacts with "Total objects/surfaces", contact frequencies ranged from 229.9 to 1517.7 contacts/h, median durations/contact ranged from < 1 to 5 s, and hourly contact durations ranged from 42.6 to 102.2 m/h. The data were analyzed for significant differences in hand contact activities as a function of (1) age, (2) location, (3) gender, and (4) hand. Significant differences (P < or = 0.05) were found for all four factors analyzed. Hourly contact durations with "Non-dietary objects/surfaces" and "Total objects/surfaces" increased with age (P = 0.01, rs = 0.42 and P = 0.005, rs = 0.46, respectively), while contact frequencies and hourly contact durations with "Wood" decreased with age (P = 0.02, rs = -0.38 and P = 0.05, rs = -0.32, respectively). Location was found to affect contact frequencies and hourly contact durations with certain objects/surfaces. For example, contact frequencies and hourly contact durations with "Fabric" were higher indoors (P = 0.02 for both), while contact frequencies and hourly contact durations with "Vegetation/Grass" were higher outdoors (P = 0.02 and P = 0.04, respectively). Girls had longer hourly contact durations with "Footwear" (P = 0.02), "Non-dietary objects/surfaces" (P = 0.03), and "Total objects/surfaces" (P = 0.01) than boys. The right hand had longer hourly contact durations with objects that are often manipulated with the hand (e.g., "Toys" (P = 0.0002)), while the left hand had longer hourly contact durations with passively touched objects/surfaces (e.g., "Clothes/Towels" (P = 0.003) and "Floor" (P = 0.04)).
View details for DOI 10.1038/sj.jes.7500480
View details for Web of Science ID 000241165900006
View details for PubMedID 16552427
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Spinel formation for stabilizing simulated nickel-laden sludge with aluminum-rich ceramic precursors
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2006; 40 (16): 5077-5083
Abstract
The feasibility of stabilizing nickel-laden sludge from commonly available Al-rich ceramic precursors was investigated and accomplished with high nickel incorporation efficiency. To simulate the process, nickel oxide was mixed alternatively with gamma-alumina, corundum, kaolinite, and mullite and was sintered from 800 to 1480 degrees C. The nickel aluminate spinel (NiAl2O4) was confirmed as the stabilization phase for nickel and crystallized with efficiencies greater than 90% for all precursors above 1250 degrees C and 3-h sintering. The nickel-incorporation reaction pathways with these precursors were identified, and the microstructure and spinel yield were investigated as a function of sintering temperature with fixed sintering time. This study has demonstrated a promising process for forming nickel spinel to stabilize nickel-laden sludge from a wide range of inexpensive ceramic precursors, which may provide an avenue for economically blending waste metal sludges via the building industry processes to reduce the environmental hazards of toxic metals. The correlation of product textures and nickel incorporation efficiencies through selection of different precursors also provides the option of tailoring property-specific products.
View details for DOI 10.1021/es052324z
View details for Web of Science ID 000239684900045
View details for PubMedID 16955910
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Video methods in the quantification of children's exposures
JOURNAL OF EXPOSURE SCIENCE AND ENVIRONMENTAL EPIDEMIOLOGY
2006; 16 (3): 287-298
Abstract
In 1994, Stanford University's Exposure Research Group (ERG) conducted its first pilot study to collect micro-level activity time series (MLATS) data for young children. The pilot study involved videotaping four children of farm workers in the Salinas Valley of California and converting their videotaped activities to valuable text files of contact behavior using video-translation techniques. These MLATS are especially useful for describing intermittent dermal (i.e., second-by-second account of surfaces and objects contacted) and non-dietary ingestion (second-by-second account of objects or hands placed in the mouth) contact behavior. Second-by-second records of children contact behavior are amenable to quantitative and statistical analysis and allow for more accurate model estimates of human exposure and dose to environmental contaminants. Activity patterns data for modeling inhalation exposure (i.e., accounts of microenvironments visited) can also be extracted from the MLATS data. Since the pilot study, ERG has collected an immense MLATS data set for 92 children using more developed and refined videotaping and video-translation methodologies. This paper describes all aspects required for the collection of MLATS including: subject recruitment techniques, videotaping and video-translation processes, and potential data analysis. This paper also describes the quality assurance steps employed for these new MLATS projects, including: training, data management, and the application of interobserver and intraobserver agreement during video translation. The discussion of these issues and ERG's experiences in dealing with them can assist other groups in the conduct of research that employs these more quantitative techniques.
View details for DOI 10.1038/sj.jea.7500459
View details for Web of Science ID 000237513600008
View details for PubMedID 16249797
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Photocatalytic oxidation of emerging contaminants: Kinetics and pathways for photocatalytic oxidation of pharmaceutical compounds
2nd European Conference on Oxidation and Reduction Technologies for Ex-Situ and In-Situ Treatment of Water, Air and Soil
SCIENCE & TECHNOLOGY NETWORK INC. 2006: 59–64
View details for Web of Science ID 000235522700009
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Effect of 200 days' sludge retention time on performance of a pilot scale submerged membrane bioreactor for high strength industrial wastewater treatment
IWA International Conference on Sustainable Development of Chemical Industries with the Environment
IWA PUBLISHING. 2006: 269–76
Abstract
A high strength industrial wastewater was treated using a pilot scale submerged membrane bioreactor (MBR) at a sludge retention time (SRT) of 200 d. The MBR was operated at a high sludge concentration of 20 g/L and a low F/M ratio of 0.11 during 300 d of operation. It was found that the MBR could achieve COD and TOC overall removal efficiencies at more than 99 and 98% TN removal. The turbidity of the permeate was consistently in the range of 0.123 to 0.136 NTU and colour254 absorbance readings varied from 0.0912 to 0.0962 a.u. cm(-1). The sludge concentration was inversely proportional to the hydraulic retention time (HRT), yielded excellent organic removal and extremely low sludge production (0.0016 kgVSS/day).
View details for DOI 10.2166/wst.2006.362
View details for Web of Science ID 000239320900033
View details for PubMedID 16862799
- Hypochlorite Degradation of CrosslinkedPolyamide Membranes: I. Changes in Chemical/Morphological Properties Journal of Membrane Science 2006; 282: 21-26
- An Efficient Bicomponent TiO2/SnO2NanofiberPhotocatalyst Fabricated by Electrospinning with a Side-by-Side Dual Spinneret Method Nano Letters 2006; 4 (7): 1081-1085
- Hypochlorite Degradation of CrosslinkedPolyamide Membranes: II. Changes in Hydrogen Bonding Behavior and Performance Journal of Membrane Science 2006; 282: 456-464
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Managing E-Government IT infrastructure: An approach combining autonomic computing and awareness based collaboration
4th International Conference on Computer and Information Technology
IEEE COMPUTER SOC. 2004: 998–1003
View details for Web of Science ID 000224461900161
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Variability in goethite surface site density: evidence from proton and carbonate sorption
JOURNAL OF COLLOID AND INTERFACE SCIENCE
2003; 268 (2): 273-287
Abstract
Goethite is a representative iron oxide in natural environments due to its abundance and thermodynamic stability and may be responsible for many surface-mediated processes, including ion retention and mobility in aqueous settings. A large variability in morphologies and specific surface areas of goethite crystals exists but little work has been done to compare surface reactivity between them. The present work offers experimental evidence for the existence of an inverse relationship between sorption capacity for protons and carbonate ions and specific surface area of goethite for three synthetic goethite preparations spanning surface area differences by a factor of 2. An explanation for this was found by assuming a variable reactive site density between preparations in direct relationship to their sorption capacity based on congruency of carbonate sorption computed on a per-site basis. Previous evidence of maximum sorption capacities supports this explanation, and site density ratios between the goethites studied here were obtained. Triple layer surface complexation modeling was successful in describing adsorption data for all goethite preparations using equal stoichiometries. A new formulation of standard state for activities of surface species based on a 1.0 mole fraction of sites on the solid allowed transformation of the conventional molar concentration-based affinity constants to values based on site occupancy. In this fashion, by applying the appropriate site density ratios, a single set of affinity constant values was found that described accurately the adsorption data for all preparations.
View details for DOI 10.1016/j.jcis.2003.07.044
View details for Web of Science ID 000187019200001
View details for PubMedID 14643228
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Association of uranyl with the cell wall of Pseudomonas fluorescens inhibits metabolism
GEOCHIMICA ET COSMOCHIMICA ACTA
2003; 67 (21): 4057-4066
View details for DOI 10.1016/S0016-7037(03)00214-X
View details for Web of Science ID 000186159000005
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Fate of uranyl in a quaternary system composed of uranyl, citrate, goethite, and Pseudomonas fluorescens
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2003; 37 (16): 3555-3559
Abstract
This study investigated the partitioning of uranyl within a quaternary system made up of uranyl, citrate, goethite, and the bacterium Pseudomonas fluorescens. In the absence of cells, uranyl was sorbed to goethite as a complex involving surface groups and/or citrate. Measurements of the evolution of CO2 indicated that the addition of bacterial cells lead to the gradual biodegradation of citrate. Throughout the biodegradation process, uranyl remained sorbed to the insoluble fraction comprised of goethite and cells. EXAFS (Extended X-ray Absorption Fine Structure) measurements showed that bacterial cells outcompeted goethite for uranyl under the experimental conditions and caused the repartitioning of uranyl from goethite to cell matter, independently from citrate degradation. Citrate degradation caused further release of uranyl from goethite surfaces, followed by subsequent association of uranyl with cells. At long equilibration times (3 months), cell lysis and phosphate release resulted in the precipitation of an autunite-like phase. This work suggests that bacterial degradation of uranyl-complexing ligands in contaminated subsurface media containing iron oxides should not necessarily lead to an increase in the mobility of uranyl.
View details for DOI 10.1021/es0210401
View details for Web of Science ID 000184803700012
View details for PubMedID 12953865
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Surface complexation modeling of carbonate effects on the adsorption of Cr(VI), Pb(II), and U(VI) on goethite
ENVIRONMENTAL SCIENCE & TECHNOLOGY
2001; 35 (19): 3849-3856
Abstract
Dissolved carbonate species are known to affect the sorption behavior of trace species. The macroscopic description of these interactions with a thermodynamic approach has been limited by the lack of data on the binary interaction between carbonate and relevant mineral surfaces. This work follows from two detailed studies of carbonate adsorption on goethite (4, 13). It shows that independent triple-layer surface complexation modeling (TLM) of carbonate adsorption allows successful descriptions of carbonate-trace element ternary sorption on this oxide, using relatively simple and optimal stoichiometries. Carbonate adsorption was considerably enhanced in the presence of Pb(II), despite an invariant total Pb(II) sorption to equilibration with up to 1% C02(g). Both the Pb(II)-carbonate system behavior and the anion-like pH adsorption behavior of U(VI) in the presence of C02 were successfully modeled using binary and ternary metal-bound surface complexes. The significant reduction of Cr(VI) adsorption edges to lower pH values in the presence of C02 was accurately simulated and explained via site competition and surface electrostatic repulsion effects on the predicted inner- and outer-sphere Cr(VI) surface complexes formed. The results of this research are highly relevant to modeling of metal transport field data and of potential soil remediation schemes using carbonate.
View details for DOI 10.1021/es001748k
View details for Web of Science ID 000171352500018
View details for PubMedID 11642443
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Surface Complexation Modeling and FTIR Study of Carbonate Adsorption to Goethite.
Journal of colloid and interface science
2001; 235 (1): 15-32
Abstract
Experimental data for carbonate adsorption onto synthetic goethite, spanning 3 orders of magnitude in carbonate concentrations, were simulated using the triple-layer surface complexation model (TLM). A single set of TLM parameters successfully described the adsorption behavior versus pH over the concentration range obtained from closed and open CO(2) conditions. An optimization analysis was performed for all possible interfacial charge configurations using FITEQL3.2. The results yielded an optimum charge allocation of 0 and -1 in the 0- and beta-planes, respectively, which suggests a monodentate complex most probably in an inner-sphere configuration (SOCOO(-beta)). Fourier transform infrared (FTIR) spectroscopic measurements on open systems at atmospheric P(CO(2)) confirmed this result by showing a clear peak split (155 cm(-1)) of the nu(3) C-O asymmetric stretching frequency of surface-bound carbonate, consistent with that reported for monodentate Co(III)-carbonato inner-sphere solution complexes. An additional Na(+)-ternary complex (SOCOONa) was invoked in the TLM construct to improve simulations of the enhanced carbonate adsorption occurring at high ionic strength and high pH. The model was successful in predicting carbonate adsorption behavior under diffferent conditions than it was calibrated for. Projections for equilibration at higher P(CO(2))'s (1-10%) than those used in this work show the potential for carbonate sorption densities of up to 2.5-3 µmol/m(2). Copyright 2001 Academic Press.
View details for DOI 10.1006/jcis.2000.7341
View details for PubMedID 11237439
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Surface complexation modeling and FTIR study of carbonate adsorption to goethite
JOURNAL OF COLLOID AND INTERFACE SCIENCE
2001; 235 (1): 15-32
View details for DOI 10.1006/jcis.2000.7341
View details for Web of Science ID 000167132300004
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Carbonate adsorption on goethite under closed and open CO2 conditions
GEOCHIMICA ET COSMOCHIMICA ACTA
2000; 64 (22): 3787-3802
View details for Web of Science ID 000165222900002
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Modeling particle transport and aggregation in a quiescent aqueous environment using the residence-time scheme
WATER RESOURCES RESEARCH
2000; 36 (8): 2249-2261
View details for Web of Science ID 000088554500021
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Development of a simulation system for a continuous flow, quiescent, aqueous environment
WATER RESEARCH
2000; 34 (5): 1734-1750
View details for Web of Science ID 000085521800040
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Comparative assessment of settlement models for municipal solid waste landfill applications
WASTE MANAGEMENT & RESEARCH
1999; 17 (5): 347-368
View details for Web of Science ID 000083456400004
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Acid/base, copper binding, and Cu2+/H+ exchange properties of a soil humic acid, an experimental and modeling study
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1999; 33 (5): 786-795
View details for Web of Science ID 000078929000035
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Neptunium(V) sorption on hematite (alpha-Fe2O3) in aqueous suspension: The effect of CO2
RADIOCHIMICA ACTA
1999; 85 (1-2): 33-48
View details for Web of Science ID 000082211100006
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Quantified mouthing activity data from a four-child pilot field study
JOURNAL OF EXPOSURE ANALYSIS AND ENVIRONMENTAL EPIDEMIOLOGY
1998; 8 (4): 543-553
View details for Web of Science ID 000165532200006
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Acid/base, copper binding, and Cu2+/H+ exchange properties of goethite, an experimental and modeling study
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1998; 32 (17): 2519-2530
View details for Web of Science ID 000075724800024
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Quantified dermal activity data from a four-child pilot field study (Reprinted from the Journal of Exposure and Environmental Epidemiology, vol 7, pg 543-552, 1997)
JOURNAL OF CLEAN TECHNOLOGY ENVIRONMENTAL TOXICOLOGY AND OCCUPATIONAL MEDICINE
1998; 7 (3): 259-268
View details for Web of Science ID 000074688500003
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Quantifying videotaped activity patterns: Video translation software and training methodologies (Reprinted from the Journal of Exposure Analysis and Environmental Epidemiology, vol 7, pg 535-542, 1997)
JOURNAL OF CLEAN TECHNOLOGY ENVIRONMENTAL TOXICOLOGY AND OCCUPATIONAL MEDICINE
1998; 7 (3): 251-258
View details for Web of Science ID 000074688500002
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Time-dependent adsorption in near coastal marine sediments: a two-step model
ADVANCES IN WATER RESOURCES
1998; 21 (6): 523-531
View details for Web of Science ID 000074156400008
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Dermal exposure: The missing link
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1998; 32 (5): 134A-137A
View details for Web of Science ID 000072307100024
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Quantified dermal activity data from a four-child pilot field study
JOURNAL OF EXPOSURE ANALYSIS AND ENVIRONMENTAL EPIDEMIOLOGY
1997; 7 (4): 543-552
Abstract
Thirty-three hours of videotape collected in a 1993 pilot study were quantified, via a video translation software application, to obtain left and right hand activity data of four children of farmworkers. Reported here are the children's contact duration and frequency for each object in their environment, duration spent in each location and activity exertion level, and frequency distributions of object contact durations. The pilot study provided valuable information for evaluating and improving videotaping and videotape translation methodologies as a means of gathering activity information that can be used to refine dermal exposure estimates. Although a larger database of children's videotaped activities for different ages and populations is needed before generalizations can be made, the data presented here are the most detailed information to date for children's micro-level dermal activities.
View details for Web of Science ID A1997XW85000009
View details for PubMedID 9306237
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Quantifying videotaped activity patterns: Video translation software and training methodologies
JOURNAL OF EXPOSURE ANALYSIS AND ENVIRONMENTAL EPIDEMIOLOGY
1997; 7 (4): 535-542
Abstract
Questionnaires and diaries, the current methods of human activity data collection, do not accurately capture the detail necessary to quantify exposure incurred through the dermal and non-dietary ingestion routes. Stanford University's Environmental Engineering and Science Program has developed methodologies and software (VideoTraq) for training video translators, determining inter-observer reliability, and translating videotaped micro-activity patterns into computer text files. VideoTraq output files contain duration, in seconds, for each combination of location, activity, and object contacted corresponding to the sequential micro-activities of a videotaped subject's contact boundary (e.g., left hand, right hand, mouth). Such output allows for detailed analyses of micro-activity data, including contact frequency and duration. When coupled with environmental concentrations, these data will allow for more accurate exposure assessments, particularly for the dermal and non-dietary ingestion exposure routes.
View details for Web of Science ID A1997XW85000008
View details for PubMedID 9306236
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Modeling leachate generation and transport in solid waste landfills
ENVIRONMENTAL TECHNOLOGY
1997; 18 (7): 669-686
View details for Web of Science ID A1997YC92700001
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Environmental impacts of solid waste landfilling
JOURNAL OF ENVIRONMENTAL MANAGEMENT
1997; 50 (1): 1-25
View details for Web of Science ID A1997WY37200001
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Cation binding predictions of surface complexation models: Effects of pH, ionic strength, cation loading, surface complex, and model fit
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1997; 188 (2): 444-472
View details for Web of Science ID A1997WW72500026
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Numerical modelling of generation and transport of gas and heat in sanitary landfills .3. Sensitivity analysis
WASTE MANAGEMENT & RESEARCH
1997; 15 (1): 87-102
View details for Web of Science ID A1997WT27100007
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Gas simulation models for solid waste landfills
CRITICAL REVIEWS IN ENVIRONMENTAL SCIENCE AND TECHNOLOGY
1997; 27 (3): 237-283
View details for Web of Science ID A1997XQ58100002
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Numerical modelling of generation and transport of gas and heat in sanitary landfills .2. Model application
WASTE MANAGEMENT & RESEARCH
1996; 14 (6): 537-551
View details for Web of Science ID A1996VZ74200004
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Numerical modelling of generation and transport of gas and heat in landfills .1. Model formulation
WASTE MANAGEMENT & RESEARCH
1996; 14 (5): 483-504
View details for Web of Science ID A1996VM35700006
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Estimating and enhancing methane yield from municipal solid waste
HAZARDOUS WASTE & HAZARDOUS MATERIALS
1996; 13 (3): 309-331
View details for Web of Science ID A1996VR16300001
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Temperature effects in modeling solid waste biodegradation
ENVIRONMENTAL TECHNOLOGY
1996; 17 (9): 915-935
View details for Web of Science ID A1996VK38700001
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Anion-exchange preparation of a U-232 radiotracer for alpha-particle liquid scintillation counting
TALANTA
1996; 43 (4): 601-605
Abstract
Daughter product ingrowths, which could act as analytical interferences, are removed from (232)U(VI) stock solutions prior to use as an alpha-particle emitting radiotracer in conjunction with detection by liquid scintillation counting. The preparative benchtop separation procedure employs elution with HCl through a BioRad AG1-X8 anion-exchange resin column, and fraction collection. The importance of the separation of the (232)U isotope from daughter products, characterized by high recovery, is illustrated by liquid scintillation energy spectra. Rapid ingrowth in the purified fraction also limits the period of time after purification in which the radiotracer is usable.
View details for Web of Science ID A1996UT76200012
View details for PubMedID 18966525
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EFFECT OF PH, NACL, AND COCKTAIL SELECTION ON U-232 LIQUID SCINTILLATION SPECTRA
ANALYTICAL CHEMISTRY
1995; 67 (21): 3893-3896
View details for Web of Science ID A1995TC80900017
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Migration and atmospheric emission of landfill gas
HAZARDOUS WASTE & HAZARDOUS MATERIALS
1995; 12 (4): 309-327
View details for Web of Science ID A1995TP78800002
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X-RAY-ABSORPTION SPECTROSCOPIC STUDIES OF CADMIUM AND SELENITE ADSORPTION ON ALUMINUM-OXIDES
LANGMUIR
1995; 11 (6): 2041-2048
View details for Web of Science ID A1995RF22300033
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MODELING THE RATE OF CADMIUM AND SELENITE ADSORPTION ON MICROPOROUS AND MESOPOROUS TRANSITION ALUMINAS
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1995; 29 (4): 1099-1108
View details for Web of Science ID A1995QP70900042
View details for PubMedID 22176419
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KINETICS OF OXIDATION OF SELENITE TO SELENATE IN THE PRESENCE OF OXYGEN, TITANIA, AND LIGHT
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1995; 29 (3): 586-594
View details for Web of Science ID A1995QJ90800020
View details for PubMedID 22200266
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A PILOT-STUDY TO COLLECT MICRO-ACTIVITY DATA OF 2-YEAR-OLD TO 4-YEAR-OLD FARM-LABOR CHILDREN IN SALINAS VALLEY, CALIFORNIA
JOURNAL OF EXPOSURE ANALYSIS AND ENVIRONMENTAL EPIDEMIOLOGY
1995; 5 (1): 21-34
Abstract
A pesticide exposure assessment pilot study was conducted in Salinas Valley, California during September, 1993. The pilot study had two main purposes: 1) to develop general methodologies for videotaping micro-activities of a population, and 2) to collect an initial database of activity patterns of two- to four-year-old farm labor children. Tools to accurately determine exposure and dose through all three pathways (dermal, ingestion, and inhalation) are needed to effectively assess and manage health risks posed by pesticides and other environmental pollutants. Eight to ten hours of videotape data were collected for each of four Mexican-American farm labor children. In addition, the researchers administered a day-after recall questionnaire to the caregivers of the children to test (for the study sample) the hypothesis that recall questionnaires are inadequate for collecting detailed information regarding dermal and hand-to-mouth exposures. The results of this study provide the first detailed set of videotape data on farm labor children, a population at high risk to pesticide exposures. In addition, this is the first project in the exposure assessment field to use direct observation videotaping for collecting micro-activity data in order to quantify dermal and ingestion exposure. The comparison of caregivers' recall of children's activities to actual videotapes from the pilot study supports the hypothesis that videotaping may greatly improve the accuracy of activity information used to compute dermal and ingestion exposures. However, as it was clear that the researchers' presence in some cases altered the activities of the subjects, further experiments need to be conducted to minimize interference of videotaping on exposure-related activities. This paper explains the selection of the study population, the methods used to implement the pilot study, and the lessons learned. While the discussion focuses on four case studies in the Mexican-American farm labor population, the data collection methods developed and the lessons learned can be applied to other populations.
View details for Web of Science ID A1995RE20000002
View details for PubMedID 7663147
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Ternary complex formation at mineral solution interfaces
NEA Workshop on Binding Models Concerning Natural Organic Substances in Performance Assessment
ORGANIZATION ECONOMIC COOPERATION & DEVELOPMENT. 1995: 181–212
View details for Web of Science ID A1995BE98U00015
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INTERACTION BETWEEN AQUEOUS URANIUM(VI) AND SULFIDE MINERALS - SPECTROSCOPIC EVIDENCE FOR SORPTION AND REDUCTION
GEOCHIMICA ET COSMOCHIMICA ACTA
1994; 58 (13): 2829-2843
View details for Web of Science ID A1994NX23700006
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COMPLEXATION OF CARBONATE SPECIES AT THE GOETHITE SURFACE - IMPLICATIONS FOR ADSORPTION OF METAL-IONS IN NATURAL-WATERS
GEOCHIMICA ET COSMOCHIMICA ACTA
1994; 58 (9): 2073-2086
View details for Web of Science ID A1994NN13700007
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HUMIC ACID GOETHITE INTERACTIONS AND THEIR EFFECT ON COPPER BINDING
6th International Meeting of the International-Humic-Substances-Society - Humic Substances in the Global Environment and Implication on Human Health
ELSEVIER SCIENCE BV. 1994: 487–492
View details for Web of Science ID A1994BB95F00060
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SOLUBILITY-PRODUCT CONSTANT AND THERMODYNAMIC PROPERTIES FOR SYNTHETIC OTAVITE, CDCO3(S), AND AQUEOUS ASSOCIATION CONSTANTS FOR THE CD(II)-CO2-H2O SYSTEM
GEOCHIMICA ET COSMOCHIMICA ACTA
1993; 57 (12): 2699-2713
View details for Web of Science ID A1993LJ98300002
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KINETIC-STUDIES OF ADSORPTION-DESORPTION OF CD AND ZN ONTO AL2O3/SOLUTION INTERFACES
WATER SCIENCE AND TECHNOLOGY
1993; 28 (7): 39-45
View details for Web of Science ID A1993NC44500006
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CD2+ UPTAKE BY CALCITE, SOLID-STATE DIFFUSION, AND THE FORMATION OF SOLID-SOLUTION - INTERFACE PROCESSES OBSERVED WITH NEAR-SURFACE SENSITIVE TECHNIQUES (XPS, LEED, AND AES)
GEOCHIMICA ET COSMOCHIMICA ACTA
1992; 56 (5): 1941-1954
View details for Web of Science ID A1992HU41300012
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COBALT(II) INTERACTIONS WITH NEAR-COASTAL MARINE-SEDIMENTS
ENVIRONMENTAL GEOLOGY AND WATER SCIENCES
1992; 19 (2): 97-111
View details for Web of Science ID A1992HG28600006
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SURFACE COMPLEXATION MODELS - AN EVALUATION OF MODEL PARAMETER-ESTIMATION USING FITEQL AND OXIDE MINERAL TITRATION DATA
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1991; 142 (2): 448-469
View details for Web of Science ID A1991EZ16300015
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INSITU X-RAY ABSORPTION STUDY OF LEAD-ION SURFACE COMPLEXES AT THE GOETHITE WATER INTERFACE
LANGMUIR
1991; 7 (2): 367-373
View details for Web of Science ID A1991EY64000029
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SPECTROSCOPIC INVESTIGATION OF PB(II) COMPLEXES AT THE GAMMA-AL2O3 WATER INTERFACE
GEOCHIMICA ET COSMOCHIMICA ACTA
1990; 54 (7): 1897-1909
View details for Web of Science ID A1990DQ21100004
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STUDY OF COPPER(II) ASSOCIATION WITH DISSOLVED ORGANIC-MATTER IN SURFACE WATERS OF 3 MEXICAN COASTAL LAGOONS
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1990; 24 (5): 683-688
View details for Web of Science ID A1990DB21900018
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XANES AND EXAFS STUDY OF AQUEOUS PB(II) ADSORBED ON OXIDE SURFACES
PHYSICA B-CONDENSED MATTER
1989; 158 (1-3): 674-675
View details for Web of Science ID A1989AE26500257
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A NUMERICAL-MODEL FOR METHANE PRODUCTION IN MANAGED SANITARY LANDFILLS
WASTE MANAGEMENT & RESEARCH
1989; 7 (1): 31-42
View details for Web of Science ID A1989U603200005
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MODELING IONIC-STRENGTH EFFECTS ON ANION ADSORPTION AT HYDROUS OXIDE SOLUTION INTERFACES
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1988; 125 (2): 717-726
View details for Web of Science ID A1988Q720200039
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MODELING GAS-PRODUCTION IN MANAGED SANITARY LANDFILLS
WASTE MANAGEMENT & RESEARCH
1988; 6 (2): 115-123
View details for Web of Science ID A1988N946100002
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THE MOUNTAIN-VIEW-CONTROLLED-LANDFILL-PROJECT FIELD EXPERIMENT
WASTE MANAGEMENT & RESEARCH
1988; 6 (2): 103-114
View details for Web of Science ID A1988N946100001
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THE FEASIBILITY OF USING SEQUENTIAL EXTRACTION TECHNIQUES FOR ARSENIC AND SELENIUM IN SOILS AND SEDIMENTS
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL
1988; 52 (2): 390-397
View details for Web of Science ID A1988N190100016
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INSITU X-RAY ABSORPTION STUDY OF SURFACE COMPLEXES - SELENIUM OXYANIONS ON ALPHA-FEOOH
SCIENCE
1987; 238 (4828): 783-786
Abstract
A novel application of x-ray absorption spectroscopy has provided structural information for ions sorbed at oxide-water interfaces. As an example, in situ extended x-ray absorption fine structure (EXAFS) measurements of adsorbed selenate and selenite ions at ah alpha-FeOOH(goethite)-water interface have been performed; these measurements show that selenate forms a weakly bonded, outer-sphere complex and that selenite forms a strongly bonded, inner-sphere complex. The selenite ion is bonded directly to the goethite surface in a bidentate fashion with two iron atoms 3.38 angstroms from the selenium atom. Adsorbed selenate has no iron atom in the second coordination shell of selenium, which indicates retention of its hydration sphere upon sorption. This method provides direct structural information for adsorbed species at solid-liquid interfaces.
View details for Web of Science ID A1987K681000027
View details for PubMedID 17814706
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MACROSCOPIC PARTITIONING COEFFICIENTS FOR METAL-ION ADSORPTION - PROTON STOICHIOMETRY AT VARIABLE PH AND ADSORPTION DENSITY
ACS SYMPOSIUM SERIES
1986; 323: 162-190
View details for Web of Science ID A1986F047300009
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MECHANISM OF LEAD-ION ADSORPTION AT THE GOETHITE-WATER INTERFACE
ACS SYMPOSIUM SERIES
1986; 323: 114-141
View details for Web of Science ID A1986F047300007
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PROTON STOICHIOMETRY FOR THE ADSORPTION OF CATIONS ON OXIDE SURFACES
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1985; 106 (1): 64-69
View details for Web of Science ID A1985ALK3100008
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A GROUNDWATER MASS-TRANSPORT AND EQUILIBRIUM CHEMISTRY MODEL FOR MULTICOMPONENT SYSTEMS
WATER RESOURCES RESEARCH
1985; 21 (8): 1095-1104
View details for Web of Science ID A1985APS6500005
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SORPTION OF LEAD ONTO 2 GRAM-NEGATIVE MARINE-BACTERIA IN SEAWATER
MARINE CHEMISTRY
1985; 15 (4): 333-344
View details for Web of Science ID A1985ADR4600006
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PARTICULATE MATTER AT THE ESTUARINE SALT-MARSH SURFACE MICROLAYER - PARTICLE-SIZE DISTRIBUTIONS AND COMPARISON TO BULK SUSPENSION
ESTUARINE COASTAL AND SHELF SCIENCE
1983; 16 (6): 689-698
View details for Web of Science ID A1983RD60500007
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TRACE-METAL ADSORPTION CHARACTERISTICS OF ESTUARINE PARTICULATE MATTER - EVALUATION OF CONTRIBUTIONS OF FE/MN OXIDE AND ORGANIC-SURFACE COATINGS
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1982; 16 (10): 660-666
View details for Web of Science ID A1982PJ47600011
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REMOVAL OF TOXIC METALS FROM POWER-GENERATION WASTE STREAMS BY ADSORPTION AND COPRECIPITATION
JOURNAL WATER POLLUTION CONTROL FEDERATION
1982; 54 (11): 1472-1481
View details for Web of Science ID A1982PN57900010
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MECHANISMS FOR TRACE-METAL ENRICHMENT AT THE SURFACE MICROLAYER IN AN ESTUARINE SALT-MARSH
MARINE CHEMISTRY
1982; 11 (3): 235-244
View details for Web of Science ID A1982NT83000004
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ACCUMULATION AND TRANSPORT OF CD, CU, AND PB IN AN ESTUARINE SALT-MARSH SURFACE MICROLAYER
LIMNOLOGY AND OCEANOGRAPHY
1982; 27 (1): 111-125
View details for Web of Science ID A1982NA27100010
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ENRICHMENT AND ASSOCIATION OF LEAD AND BACTERIA AT PARTICULATE SURFACES IN A SALT-MARSH SURFACE-LAYER
JOURNAL OF MARINE RESEARCH
1982; 40 (4): 1201-1211
View details for Web of Science ID A1982QH61400013
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CONCEPTUAL-MODEL FOR METAL-LIGAND-SURFACE INTERACTIONS DURING ADSORPTION
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1981; 15 (9): 1050-1057
View details for Web of Science ID A1981MD81900009
View details for PubMedID 22284108
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CHEMICAL SPECIATION OF TRACE-METALS AT THE AIR-SEA INTERFACE - THE APPLICATION OF AN EQUILIBRIUM-MODEL
ENVIRONMENTAL GEOLOGY
1981; 3 (5): 293-314
View details for Web of Science ID A1981MJ52700005
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COMPETITIVE ADSORPTION OF CD, CU, ZN, AND PB ON AMORPHOUS IRON OXYHYDROXIDE
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1981; 83 (2): 410-419
View details for Web of Science ID A1981MK44200010
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THE BIOGEOCHEMISTRY OF THE AIR-SEA INTERFACE
ANNUAL REVIEW OF EARTH AND PLANETARY SCIENCES
1981; 9: 449-486
View details for Web of Science ID A1981LR39700016
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MULTIPLE-SITE ADSORPTION OF CD, CU, ZN, AND PB ON AMORPHOUS IRON OXYHYDROXIDE
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1981; 79 (1): 209-221
View details for Web of Science ID A1981KZ19900022
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SURFACE-IONIZATION AND COMPLEXATION AT THE OXIDE-WATER INTERFACE .3. ADSORPTION OF ANIONS
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1980; 74 (1): 32-43
View details for Web of Science ID A1980JH16000005
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LANDFILL MANAGEMENT WITH MOISTURE CONTROL
JOURNAL OF THE ENVIRONMENTAL ENGINEERING DIVISION-ASCE
1979; 105 (2): 337-355
View details for Web of Science ID A1979GP13800013
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NUMERICAL-SIMULATION OF GAS-FLOW IN SANITARY LANDFILLS
JOURNAL OF THE ENVIRONMENTAL ENGINEERING DIVISION-ASCE
1979; 105 (5): 927-945
View details for Web of Science ID A1979HQ62800010
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PARTICULATE MATTER - ITS ASSOCIATION WITH MICROORGANISMS AND TRACE-METALS IN AN ESTUARINE SALT-MARSH MICROLAYER
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1979; 13 (12): 1522-1525
View details for Web of Science ID A1979HW20200023
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INVESTIGATION OF SOLUBLE ORGANIC NITROGEN-COMPOUNDS IN MUNICIPAL SECONDARY EFFLUENT
JOURNAL WATER POLLUTION CONTROL FEDERATION
1978; 50 (11): 2522-2529
View details for Web of Science ID A1978FV01600012
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COMPUTER-SIMULATION OF CONDUCTOMETRIC AND POTENTIOMETRIC TITRATIONS OF SURFACE GROUPS ON IONIZABLE LATEXES
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1978; 65 (2): 331-344
View details for Web of Science ID A1978FD95100015
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SURFACE IONIZATION AND COMPLEXATION AT OXIDE-WATER INTERFACE .2. SURFACE PROPERTIES OF AMORPHOUS IRON OXYHYDROXIDE AND ADSORPTION OF METAL-IONS
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1978; 67 (1): 90-107
View details for Web of Science ID A1978FX10100010
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EFFECT OF ADSORBED COMPLEXING LIGANDS ON TRACE-METAL UPTAKE BY HYDROUS OXIDES
ENVIRONMENTAL SCIENCE & TECHNOLOGY
1978; 12 (12): 1309-1315
View details for Web of Science ID A1978FU74500019
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SURFACE IONIZATION AND COMPLEXATION AT OXIDE-WATER INTERFACE .1. COMPUTATION OF ELECTRICAL DOUBLE-LAYER PROPERTIES IN SIMPLE ELECTROLYTES
JOURNAL OF COLLOID AND INTERFACE SCIENCE
1978; 63 (3): 480-499
View details for Web of Science ID A1978EP71600009