RESUMEN
Trichloroethylene (TCE) is one of the most ubiquitous halogenated organic compounds of concerns of carcinogens in groundwater in Taiwan. Bioremediation has been recognized as a cost-effective approach in reducing TCE concentration. Five pilot-scale wells were constructed to monitor TCE concentrations in contaminated groundwater. With injection of EOS®, TCE was effectively degraded to 42%-93% by the end of 175 days. The biostimulation with EOS® was useful in establishing a micro-site anaerobic but with limited contribution. Dilution of the aquifer movement also caused the TCE reduction among injection and monitoring wells. The degradability was affected by the location and the proximity from the injection well. TCE concentrations found to be negatively correlated with the associated Dehalococcoides spp. and functional genes levels. Dhc concentration of 108 copies L-1 caused the initial 40% of TCE degradation. The well with the optimal degradation owned tceA of 109â¯cells L-1. T-RFLP results indicate the wells with the superior TCE degradability also performed the highest Shannon index number (means the highest diversity), which occurred on the same day that Dhc levels started to enlarge. Desulfovibrio desulfuricans and Desulfuromonas chloroethenica were predominant species identified in the T-RFLP fingerprint profile. In brief, a variety of different factors including well locations, geochemical indicators, and microbial contribution were useful to explain the site-specific optimal TCE remediation approach. The consistence among TCE degradation, Dhc growing pattern, functional gene levels, and the dynamics of the microbial community structure present the novelty of this study.
Asunto(s)
Restauración y Remediación Ambiental/métodos , Tricloroetileno/metabolismo , Contaminantes Químicos del Agua/metabolismo , Biodegradación Ambiental , Chloroflexi/metabolismo , Agua Subterránea/química , Halogenación , Microbiota , Taiwán , Tricloroetileno/análisis , Tricloroetileno/química , Contaminantes Químicos del Agua/análisisRESUMEN
A new model is developed to predict the competitive adsorption isotherms of atrazine, methyl tertiary butyl ether (MTBE), 2-methylisoborneol (2-MIB) and 2,4,6-trichlorophenol onto activated carbons (ACs) in natural water. Based on the Polanyi-Dubinin (PD) equation, with the limiting pore volume of adsorbent estimated from the pore size distribution data, and the Ideal adsorbed solution theory - equivalent background compound (IAST-EBC) model approximation, the model takes into account both the properties of ACs and the impact of natural organic matters in water. Only one set of isotherm in deionized water and one set in natural water are needed to obtain the parameters for the prediction of adsorption isotherms onto different ACs in natural water. The model was employed for the predictions of adsorption capacities for atrazine, MTBE, 2-MIB and 2,4,6-trichlorophenol onto 14 ACs in 22 synthetic and natural waters reported in 9 references, with errors between 14.9% and 44.5% SDEV only. The results suggest that in the proposed PD-IAST-EBC approach, prediction of adsorption capacity for organic compounds onto different ACs in the same natural water is feasible, if the ACs are thermally activated with known pore size information. The model may provide a simple approach for the prediction of adsorption of organic compounds in natural water, and thus greatly reduces the effort required for water utilities when change of AC is needed.
Asunto(s)
Carbón Orgánico , Agua , Adsorción , Compuestos Orgánicos , Contaminantes Químicos del Agua , Purificación del AguaRESUMEN
The addition of powdered activated carbon (PAC) is an effective measure to cope with seasonal taste and odor (T&O) problems caused by 2-methylisoborneol (2-MIB) and trans-1, 10-dimethyl-trans-9-decalol (geosmin) in drinking water. Some T&O problems are episodic in nature, and generally require rapid responses. This paper proposed a simplified approach for the application of the homogenous surface diffusion model (HSDM) to predict the appropriate PAC doses for the removal of 2-MIB. Equilibrium and kinetic experiments were performed for 2-MIB adsorption onto five PACs in three source waters. The simplified HSDM approach was compared with the experimental data, by assigning the Freundlich 1/n value in the range of 0.1-1.0 and obtaining the Freundlich equilibrium parameter K value through a 6-hr adsorption kinetic test. The model describes the kinetic adsorption data very well for all of the tested PACs in different source waters. The results were validated using the data obtained from one full scale water treatment plant, and the differences between the predicted and observed results were within 10% range. This simplified HSDM approach may be applied for the rapid determination of PAC doses for water treatment plants when faced with 2-MIB episodes in source waters.
Asunto(s)
Canfanos/química , Carbono/química , Modelos Teóricos , Contaminantes Químicos del Agua/química , Purificación del Agua/métodos , Adsorción , Difusión , CinéticaRESUMEN
A new model approach is developed to predict the adsorption isotherms of low-molecular-weight nonpolar organic compounds (LMWNPOCs) onto activated carbons (ACs). The model is based on the Polanyi-Dubinin (PD) equation, with the limiting pore volume of adsorbent estimated from the pore size distribution (PSD) data, and the adsorption affinity of adsorbate described by the molecular connectivity index (MCI). To obtain the MCI parameters, the model was first tested for the adsorption of 34 LMWNPOCs primarily on F400 AC from 3 reports. The models fit the experimental data well, with only 39.2% of errors. The approach was further employed to predict the adsorption capacity of 40 LMWNPOCs on F400 AC, 12 LMWNPOCs onto 9 other ACs, and 8 LMWNPOCs onto 5 ACs with unknown PSD, with the errors of 41.9%, showing the model being reasonable. The model approach may provide a simple means for predicting adsorption capacities of LMWNPOCs onto different ACs.
Asunto(s)
Carbón Orgánico/química , Filtración/métodos , Contaminantes Químicos del Agua/química , Adsorción , Modelos TeóricosRESUMEN
Black carbons (BCs) may sequester non-ionic organic compounds by adsorption and/or partition to varying extents. Up to now, no experimental method has been developed to accurately resolve the combined adsorption and partition capacity of a compound on a BC. In this study, a unique "adsorptive displacement method" is introduced to reliably resolve the adsorption and partition components for a solute-BC system. It estimates the solute adsorption on a BC by the use of an adsorptive displacer to displace the adsorbed target solute into the solution phase. The method is validated by tests with uses of activated carbon as the model carbonaceous adsorbent, soil organic matter as the model carbonaceous partition phase, o-xylene and 1,2,3-trichlorobenzene as the reference solutes, and p-nitrophenol as the adsorptive displacer. Thereafter, the adsorption-partition resolution was completed for the two solutes on selected model BCs: four biochars and two National Institute of Standards and Technology (NIST) standard soots (SRM-2975 and SRM-1650b). The adsorption and partition components resolved for selected solutes with given BCs and their dependences upon solute properties enable one to cross-check the sorption data of other solutes on the same BCs. The resolved components also provide a theoretical basis for exploring the potential modes and extents of different solute uptakes by given BCs in natural systems.
Asunto(s)
Compuestos Orgánicos/química , Hollín/análisis , Adsorción , Carbón Orgánico/química , Clorobencenos/química , Nitrofenoles/química , Xilenos/químicaRESUMEN
In view of the scarcity of the lipid-water partition coefficients (Ktw) for organic compounds, the logKtw values for many environmental contaminants were measured using ultra-pure triolein as the model lipid. Classes of compounds studied include alkyl benzenes, halogenated benzenes, short-chain chlorinated hydrocarbons, polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and organochlorine pesticides. In addition to logKtw determination, the uptakes of these compounds from water by a dry algal species were measured to evaluate the lipid effect on the algal uptake. The measured logKtw are closely related to their respective logKow (octanol-water), with logKow=1.9 to 6.5. A significant difference is observed between the present and early measured logKtw for compounds with logKow>â¼5, which is attributed to the presence and absence of a triolein microemulsion in water affecting the solute partitioning. The observed lipid-normalized algae-water distribution coefficients (logKaw/lipid) are virtually identical to the respective logKtw values, which manifests the dominant lipid-partition effect of the compounds with algae.
Asunto(s)
Chlorella/metabolismo , Contaminantes Ambientales/metabolismo , Compuestos Orgánicos/metabolismo , Adsorción , Chlorella/química , Contaminantes Ambientales/química , Cinética , Lípidos , Octanoles/química , Compuestos Orgánicos/química , Solubilidad , Agua/químicaRESUMEN
The sorption of phenanthrene (PHN) to relatively pure soil humic acids (HAs) was investigated to assess the suitability of the soil HA as a surrogate sorbent for the soil organic matter (SOM). The HAs were prepared in both freeze-dried and air-dried forms. The two forms of HAs from the same source are similar in composition but the freeze-dried HAs exhibit a significantly higher initial surface area (SA) (3.86-4.59 m(2)/g); the SAs of air-dried HAs are below 0.1 m(2)/g. However, the SAs of freeze-dried HAs are not stable upon contact with water; the samples lose practically all the SA after 4 days of immersion in water. The PHN sorption to both forms of HAs is practically linear, whether a co-solute is present or not. The sorption linearity observed with the present freeze-dried HAs is in sharp contrast with the allegedly nonlinear PHN sorption on similar freeze-dried HAs as presented by others.