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1.
In the present study, a novel adsorbent, poly (2‐hydroxyethylmethacrylate‐hydroxyapatite) [P(HEMA‐Hap)], was prepared and characterized. The synthesis was achieved by means of free‐radical polymerization and a number of structural characterization methods, including FT‐IR, XRD, TGA, SEM, BET‐porosity, and swelling tests. Pb2+ adsorption was performed using a series of pH, time, and temperature ranges. The reusability of the composite was also tested. The results obtained indicated that the novel adsorbent is able to bind Pb2+ ions with strong chemical affinity. The adsorption results were fitted to the classic Langmuir, Freundlich, and Dubinin–Radushkevich (D–R) sorption models. Thermodynamic parameters obtained demonstrated that the sorption process was spontaneous (ΔG < 0), endothermic (ΔH > 0), as expected. The process was also consistent with the pseudo‐second‐order model, and chemical adsorption was determined to be the rate‐controlling step. It was also shown that the composite could be used for five consecutive adsorption processes.  相似文献   

2.
Soil moisture has a pronounced effect on earth surface processes. Global soil moisture is strongly driven by climate, whereas at finer scales, the role of non‐climatic drivers becomes more important. We provide insights into the significance of soil and land surface properties in landscape‐scale soil moisture variation by utilizing high‐resolution light detection and ranging (LiDAR) data and extensive field investigations. The data consist of 1200 study plots located in a high‐latitude landscape of mountain tundra in north‐western Finland. We measured the plots three times during growing season 2016 with a hand‐held time‐domain reflectometry sensor. To model soil moisture and its temporal variation, we used four statistical modelling methods: generalized linear models, generalized additive models, boosted regression trees, and random forests. The model fit of the soil moisture models were R2 = 0.60 and root mean square error (RMSE) 8.04 VWC% on average, while the temporal variation models showed a lower fit of R2 = 0.25 and RMSE 13.11 CV%. The predictive performances for the former were R2 = 0.47 and RMSE 9.34 VWC%, and for the latter R2 = 0.01 and RMSE 15.29 CV%. Results were similar across the modelling methods, demonstrating a consistent pattern. Soil moisture and its temporal variation showed strong heterogeneity over short distances; therefore, soil moisture modelling benefits from high‐resolution predictors, such as LiDAR based variables. In the soil moisture models, the strongest predictor was SAGA (System for Automated Geoscientific Analyses) wetness index (SWI), based on a 1 m2 digital terrain model derived from LiDAR data, which outperformed soil predictors. Thus, our study supports the use of LiDAR based SWI in explaining fine‐scale soil moisture variation. In the temporal variation models, the strongest predictor was the field‐quantified organic layer depth variable. Our results show that spatial soil moisture predictions can be based on soil and land surface properties, yet the temporal models require further investigation. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   

3.
This study challenges the use of three nature‐inspired algorithms as learning frameworks of the adaptive‐neuro‐fuzzy inference system (ANFIS) machine learning model for short‐term modeling of dissolved oxygen (DO) concentrations. Particle swarm optimization (PSO), butterfly optimization algorithm (BOA), and biogeography‐based optimization (BBO) are employed for developing predictive ANFIS models using seasonal 15 min data collected from the Rock Creek River in Washington, DC. Four independent variables are used as model inputs including water temperature (T), river discharge (Q), specific conductance (SC), and pH. The Mallow's Cp and R2 parameters are used for choosing the best input parameters for the models. The models are assessed by several statistics such as the coefficient of determination (R2), root‐mean‐square error (RMSE), Nash–Sutcliffe efficiency, mean absolute error, and the percent bias. The results indicate that the performance of all‐nature‐inspired algorithms is close to each other. However, based on the calculated RMSE, they enhance the accuracy of standard ANFIS in the spring, summer, fall, and winter around 13.79%, 15.94%, 6.25%, and 12.74%, respectively. Overall, the ANFIS‐PSO and ANFIS‐BOA provide slightly better results than the other ANFIS models.  相似文献   

4.
A start‐up study for biohydrogen production from palm oil mill effluent (POME) is carried out in a pilot‐scale up‐flow anaerobic sludge blanket fixed‐film reactor (UASFF). A substrate with a chemical oxygen demand (COD) of 30 g L?1 is used, starting with molasses solution for 30 days and followed by a 10% v/v increment of POME/molasses ratio. At 100% POME, a hydrogen content of 80%, hydrogen production rate of 36 L H2 per day, and maximum COD removal of 48.7% are achieved. Bio‐kinetic coefficients of Monod, first‐order, Grau second‐order, and Stover‐Kincannon kinetic models are calculated to describe the performance of the system. The steady‐state data with 100% POME shows that Monod and Stover‐Kincannon models with bio‐kinetic coefficients of half‐velocity constant (Ks) of 6000 mg COD L?1, microbial decay rate (Kd) of 0.0015 per day, growth yield constant (Y) of 0.786 mg volatile suspended solids (VSS)/mg COD, specific biomass growth rate (μmax) of 0.568 per day, and substrate consumption rate of (Umax) 3.98 g/L day could be considered as superior models with correlation coefficients (R2) of 0.918 and 0.989, respectively, compared to first‐order and Grau's second‐order models with coefficients of K1 1.08 per day, R2 0.739, and K2s 1.69 per day, a = 7.0 per day, b = 0.847.  相似文献   

5.
In this study, seven types of first‐order and one‐variable grey differential equation model (abbreviated as GM (1, 1) model) were used to forecast hourly roadside particulate matter (PM) including PM10 and PM2.5 concentrations in Taipei County of Taiwan. Their forecasting performance was also compared. The results indicated that the minimum mean absolute percentage error (MAPE), mean squared error (MSE), root mean squared error (RMSE), and maximum correlation coefficient (R) was 11.70%, 60.06, 7.75, and 0.90%, respectively when forecasting PM10. When forecasting PM2.5, the minimum MAPE, MSE, RMSE, and maximum R‐value of 16.33%, 29.78, 5.46, and 0.90, respectively could be achieved. All statistical values revealed that the forecasting performance of GM (1, 1, x(0)), GM (1, 1, a), and GM (1, 1, b) outperformed other GM (1, 1) models. According to the results, it revealed that GM (1, 1) was an efficiently early warning tool for providing PM information to the roadside inhabitants.  相似文献   

6.
In this study, untreated and treated wood fly ash (WA) was used as a low‐cost sorbent in batch sorption tests to investigate the removal of organic pollutants from a real wastewater generated by cleaning/washing of machinery in a wood‐laminate floor industry in Sweden. The experiments focused on the effect of the WA dosage and particle size on the removal efficiency for organic compounds. With a WA dosage of 160 g L?1 and a particle size less than 1 mm, the reductions of chemical oxygen demand (COD), biologic oxygen demand, and total organic carbon were 37 ± 0.4, 24 ± 0.4, and 30 ± 0.3%, respectively. Pre‐treatment of WA with hot water improved the COD removal efficiency by absorption from 37 ± 0.4 to 42 ± 1.6% when the same dosage (160 g L?1) was applied. Sorption isotherm and sorption kinetics for COD using untreated WA can be explained by Freundlich isotherm and pseudo‐second‐order kinetic models. Intra‐particle diffusion model indicates that pore diffusion is not the rate‐limiting step for COD removal. Based on the experimental data, WA could be used as an alternative low‐cost sorption media/filter for removal of organic compounds from real industrial wastewater.  相似文献   

7.
To improve quantitative understanding of mixed‐land‐use impacts on nutrient yields, a nested‐scale experimental watershed study design (n = 5) was applied in a 303(d), clean water act impaired urbanizing watershed of the lower Missouri River Basin, USA. From 2010 to 2013, water samples (n = 858 sample days per site) were analysed for total inorganic nitrogen (TIN‐N), nitrite (NO2–N) nitrate (NO3–N), ammonia (NH3–N), and total phosphorus (TP‐P). Annual, seasonal, and monthly flow‐weighted concentrations (FWCs) and nutrient yields were estimated. Mean nutrient concentrations were highest where agricultural land use comprised 58% of the drainage area (NH3 = 0.111 mg/l; NO2 = 0.045 mg/l; NO3 = 0.684 mg/l, TIN = 0.840 mg/l; TP = 0.127 mg/l). Average TP‐P increased by 15% with 20% increased urban land use area. Highly variable annual precipitation was observed during the study with highest nutrient yields during 2010 (record setting wet year) and lowest nutrient yields during 2012 (extreme drought year). Annual TIN‐N and TP‐P yields exceeded 10.3 and 2.04 kg ha?1 yr?1 from the agricultural dominated headwaters. Mean annual NH3–N, NO2–N, NO3–N, TIN‐N, and TP‐P yields were 0.742, 0.400, 4.24, 5.38, and 0.979 kg ha?1 yr?1, respectively near the watershed outlet. Precipitation accounted for the majority of the explained variance in nutrient yields (R2 values from 0.68 to 0.85). Nutrient yields were also dependent on annual precipitation of the preceding year (R2 values from 0.87 to 0.91) thus enforcing the great complexity of variable mixed‐land‐use mediated source‐sink nutrient yield relationships. Study results better inform land managers and best management practices designed to mitigate nutrient pollution issues in mixed‐land‐use freshwater ecosystems. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

8.
Concentration‐discharge (c‐Q) plots are routinely used as an integrated signal of watershed response to infer solute sources and travel pathways. However, the interpretation of c‐Q data can be difficult unless these data are fitted using statistical models. Such models are frequently applied for geogenic solutes, but it is unclear to what extent they might aid in the investigation of nutrient export patterns, particularly for total dissolved phosphorus (TDP) which is a critical driver of downstream eutrophication problems. The goal of the present study was therefore to statistically model c‐Q relations (where c is TDP concentrations) in a set of contrasting watersheds in the Northern Great Plains—ranging in size from 0.2 to 1000+ km2—to assess the controls of landscape properties on TDP transport dynamics. Six statistical models were fitted to c‐Q data, notably (a) one linear model, (b) one model assuming that c‐Q relations are driven by the mixing of end‐member waters from different landscape locations (i.e., hydrograph separation), (c) one model relying on a biogeochemical stationarity hypothesis (i.e., power law), (d) one model hypothesizing that c‐Q relations change as a function of the solute subsurface contact time (i.e., hyperbolic model), and (e) two models assuming that solute fluxes are mostly dependent on reaction rates (i.e., chemical models). Model performance ranged from mediocre (R2 < 0.2) to very good (R2 > 0.9), but the hydrograph separation model seemed most universal. No watershed was found to exhibit chemostatic behaviour, but many showed signs of dilution or enrichment behaviour. A tendency toward a multi‐model fit and better model performance was observed for watersheds with moderate slope and higher effective drainage area. The relatively poor model performance obtained outside these conditions illustrates the likely importance of controls on TDP concentrations in the region that are independent of flow dynamics.  相似文献   

9.
Sorption behavior of Lanaset Red (LR) G on lentil straw (LS) was studied as a function of particle size, adsorbent dose, initial pH value, initial dye concentration, and contact time. Sorption kinetics data was well described by logistic model. Modified logistic equation can be used to explain effects of initial dye concentrations and contact time on the sorption of LR G with high R2 value. Freundlich model was found to be excellent in representing the equilibrium data. Thermodynamic parameters like free energy (ΔG0), enthalpy (ΔH0), and entropy (ΔS0) were calculated by the use of Langmuir constant. Thermodynamic data showed that the sorption processes were spontaneous and endothermic in nature. Desorption process suggested that strong binding and weak interactions could be formed between adsorbent surface and dye molecules. Results revealed that LS has a remarkable potential for the sorption of LR G.  相似文献   

10.
This study simulates how spatial variations in particle‐size emissions from a playa affect bulk and size‐resolved dust concentration profiles during two contrasting wind erosion events (a small local and a large regional event) in the Channel Country, Lake Eyre Basin, Australia. The regional event had higher dust concentration as a result of stronger frontal winds and higher erodibility across the playa. For each event, two emission scenarios are simulated to determine if measured size‐resolved dust concentration profiles can be explained by spatial variability in source area emissions. The first scenario assumes that particle‐size emissions from source areas occur at a uniform rate, while the second scenario assumes that particle‐size emissions vary between and within source areas. The uniform emission scenario, reproduced measured bulk dust concentration profiles (R2 = 0·93 regional and R2 = 0·81 local), however simulated size‐resolved dust concentration profiles had poor statistical fits to measured size‐resolved profiles for each size class (the highest were R2 = 0·5 regional and R2 = 0·3 local). For the differential particle‐size emission scenario, the fit to the measured bulk dust concentration profiles is improved (R2 = 0·97 regional and R2 = 0·83 local). However, the fit to the size‐resolved profiles improved dramatically, with the lowest being R2 = 0·89 (regional) and R2 = 0·80 (local). Particle‐size emission models should therefore be tested against both bulk and size‐resolved dust concentration profiles, since if only bulk dust concentration profiles are used model performance may be over‐stated. As the source areas in the first 90 m upwind of the tower were similar for both events, the percentage contributions of each particle‐size class to total emissions can be compared. The contribution of each particle‐size class was similar even though the wind speed, turbulence and dust concentrations were significantly different; suggesting that the contribution of each particle‐size to the total emitted dusts is not related to wind speed and turbulence. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

11.
A continuous Soil Conservation Service (SCS) curve number (CN) method that considers time‐varied SCS CN values was developed based on the original SCS CN method with a revised soil moisture accounting approach to estimate run‐off depth for long‐term discontinuous storm events. The method was applied to spatially distributed long‐term hydrologic simulation of rainfall‐run‐off flow with an underlying assumption for its spatial variability using a geographic information systems‐based spatially distributed Clark's unit hydrograph method (Distributed‐Clark; hybrid hydrologic model), which is a simple few parameter run‐off routing method for input of spatiotemporally varied run‐off depth, incorporating conditional unit hydrograph adoption for different run‐off precipitation depth‐based direct run‐off flow convolution. Case studies of spatially distributed long‐term (total of 6 years) hydrologic simulation for four river basins using daily NEXRAD quantitative precipitation estimations demonstrate overall performances of Nash–Sutcliffe efficiency (ENS) 0.62, coefficient of determination (R2) 0.64, and percent bias 0.33% in direct run‐off and ENS 0.71, R2 0.72, and percent bias 0.15% in total streamflow for model result comparison against observed streamflow. These results show better fit (improvement in ENS of 42.0% and R2 of 33.3% for total streamflow) than the same model using spatially averaged gauged rainfall. Incorporation of logic for conditional initial abstraction in a continuous SCS CN method, which can accommodate initial run‐off loss amounts based on previous rainfall, slightly enhances model simulation performance; both ENS and R2 increased by 1.4% for total streamflow in a 4‐year calibration period. A continuous SCS CN method‐based hybrid hydrologic model presented in this study is, therefore, potentially significant to improved implementation of long‐term hydrologic applications for spatially distributed rainfall‐run‐off generation and routing, as a relatively simple hydrologic modelling approach for the use of more reliable gridded types of quantitative precipitation estimations.  相似文献   

12.
Using batch method, the adsorption of thallium(I) ions from aqueous solutions on eucalyptus leaves powder, as a low cost adsorbent, was studied. The effect of various modification of considered adsorbent on the adsorption percentage of Tl(I) is an important feature of this study. The results showed that the unmodified and acidic modified adsorbent are the poor adsorbents for the Tl(I) ions while basic modified adsorbent is a suitable adsorbent. Also, the effect of some experimental conditions such as solution initial pH, agitation speed, contact time, sorbent dosage, temperature, particle size, and thallium initial concentration was studied. The results showed that the adsorption percentage depends on the conditions and the process is strongly pH‐dependent. The satisfactory adsorption percentage of Tl(I) ions, 81.5%, obtained at 25 ± 1°C. The equilibrium data agreed fairly better with Langmuir isotherm than Freundlich and Temkin models. The value of qm that was obtained by extrapolation method is 80.65 mg g?1. Separation factor values, RL, showed that eucalyptus leaves powder is favorable for the sorption of Tl(I). The negative values of ΔH0 and ΔS0 showed that the Tl(I) sorption is an exothermic process and along with decrease of randomness at the solid–solution interface during sorption, respectively.  相似文献   

13.
This study was conducted under the USDA‐Conservation Effects Assessment Project (CEAP) in the Cheney Lake watershed in south‐central Kansas. The Cheney Lake watershed has been identified as ‘impaired waters’ under Section 303(d) of the Federal Clean Water Act for sediments and total phosphorus. The USDA‐CEAP seeks to quantify environmental benefits of conservation programmes on water quality by monitoring and modelling. Two of the most widely used USDA watershed‐scale models are Annualized AGricultural Non‐Point Source (AnnAGNPS) and Soil and Water Assessment Tool (SWAT). The objectives of this study were to compare hydrology, sediment, and total phosphorus simulation results from AnnAGNPS and SWAT in separate calibration and validation watersheds. Models were calibrated in Red Rock Creek watershed and validated in Goose Creek watershed, both sub‐watersheds of the Cheney Lake watershed. Forty‐five months (January 1997 to September 2000) of monthly measured flow and water quality data were used to evaluate the two models. Both models generally provided from fair to very good correlation and model efficiency for simulating surface runoff and sediment yield during calibration and validation (correlation coefficient; R2, from 0·50 to 0·89, Nash Sutcliffe efficiency index, E, from 0·47 to 0·73, root mean square error, RMSE, from 0·25 to 0·45 m3 s?1 for flow, from 158 to 312 Mg for sediment yield). Total phosphorus predictions from calibration and validation of SWAT indicated good correlation and model efficiency (R2 from 0·60 to 0·70, E from 0·63 to 0·68) while total phosphorus predictions from validation of AnnAGNPS were from unsatisfactory to very good (R2 from 0·60 to 0·77, E from ? 2·38 to 0·32). The root mean square error–observations standard deviation ratio (RSR) was estimated as excellent (from 0·08 to 0·25) for the all model simulated parameters during the calibration and validation study. The percentage bias (PBIAS) of the model simulated parameters varied from unsatisfactory to excellent (from 128 to 3). This study determined SWAT to be the most appropriate model for this watershed based on calibration and validation results. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

14.
This paper deals with kinetics and equilibrium studies on the adsorption of arsenic species from simulated groundwater containing arsenic (As(III)/As(V), 1:1), Fe, and Mn in concentrations of 0.188, 2.8, and 0.6 mg/L, respectively, by Ca2+ impregnated granular activated charcoal (GAC‐Ca). Effects of agitation period and initial arsenic concentration on the removal of arsenic species have also been described. Although, most of the arsenic species are adsorbed within 10 h of agitation, equilibrium reaches after ~24 h. Amongst various kinetic models investigated, the pseudo second order model is more adequate to explain the adsorption kinetics and film diffusion is found to be the rate controlling step for the adsorption of arsenic species on GAC‐Ca. Freundlich isotherm is adequate to explain the adsorption equilibrium. However, empirical polynomial isotherm gives more accurate prediction on equilibrium specific uptakes of arsenic species. Maximum specific uptake (qmax) for the adsorption of As(T) as obtained from Langmuir isotherm is 135 µg/g.  相似文献   

15.
A seaweed‐waste material resulting from the processing of Ascophyllum nodosum was previously shown to be very efficient at removing Zn(II), Ni(II) and Al(III) both in single and multi‐metal waste streams. In this study, the regeneration of the biosorbent using an acid wash resulted in the release of high metal concentrations during multiple desorption cycles. Maximum desorption efficiencies (DE) of 183, 122 and 91% were achieved for Zn(II), Ni(II) and Al(III), respectively, for subsequent metal loading cycles, significantly exceeding the desorption rates observed for conventional sorbents. The regeneration of the sorbent was accomplished with very little loss in metal removal efficiency (RE) for both single and multi‐metal systems. Values of 92, 96 and 94% RE were achieved for Zn(II), Ni(II) and Al(III), respectively, for the 5th sorption cycle in single metal aqueous solutions. A slight decrease was observed for the same metals in multi‐metal systems with maximum REs of 85, 82 and 82% for Zn(II), Ni(II) and Al(III), respectively. This study showed that the novel sorbent derived from a seaweed industrial waste would be suitable for multiple metal sorption cycles without any significant loss in RE.  相似文献   

16.
In this paper, we present MHYDAS‐Erosion, a dynamic and distributed single‐storm water erosion model developed as a module of the existing hydrological MHYDAS model. As with many catchment erosion models, MHYDAS‐Erosion is able to simulate sediment transport, erosion and deposition by rill and interrill processes. Its originality stems from its capacity to integrate the impact of land management practices (LMP) as key elements controlling the sedimentological connectivity in agricultural catchments. To this end, the water‐sediment pathways are first determined by a specific process‐oriented procedure defined and controlled by the user, which makes the integration of LMP easier. The LMP dynamic behaviours are then integrated into the model as a time‐dependent function of hydrological variables and LMP characteristics. The first version of the model was implemented for vegetative filters and tested using water and sediment discharge measurements at three nested scales of a densely instrumented catchment (Roujan, OMERE Observatory, southern France). The results of discharge and soil loss for simulated rainfall events have been found to acceptably compare with available data. The average R2 values for water and sediment discharge are 0·82 and 0·83, respectively. The sensitivity of the model to changes in the proportion of LMP was assessed for a single rain event by considering three scenarios of the Roujan catchment management with vegetative filters: 0% (Scenario 1), 18% (Scenario 2, real case) and 100% (Scenario 3). Compared to Scenario 2 (real case), soil losses decreased for Scenario 3 by 65% on the agricultural plot scale, 62% on the sub‐catchment scale and 45% at the outlet of the catchment and increased for Scenario 1 by 0% on the plot scale, 26% on the sub‐catchment scale and 18% at the outlet of the catchment. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

17.
Tropospheric (ground‐level) ozone has adverse effects on human health and environment. In this study, next day's maximum 1‐h average ozone concentrations in Istanbul were predicted using multi‐layer perceptron (MLP) type artificial neural networks (ANNs). Nine meteorological parameters and nine air pollutant concentrations were utilized as inputs. The total 578 datasets were divided into three groups: training, cross‐validation, and testing. When all the 18 inputs were used, the best performance was obtained with a network containing one hidden layer with 24 neurons. The transfer function was hyperbolic tangent. The correlation coefficient (R), mean absolute error (MAE), root mean squared error (RMSE), and index of agreement or Willmott's Index (d2) for the testing data were 0.90, 8.78 µg/m3, 11.15 µg/m3, and 0.95, respectively. Sensitivity analysis has indicated that the persistence information (current day's maximum and average ozone concentrations), NO concentration, average temperature, PM10, maximum temperature, sunshine time, wind direction, and solar radiation were the most important input parameters. The values of R, MAE, RMSE, and d2 did not change considerably for the MLP model using only these nine inputs. The performances of the MLP models were compared with those of regression models (i.e., multiple linear regression and multiple non‐linear regression). It has been found that there was no significant difference between the ANN and regression modeling techniques for the forecasting of ozone concentrations in Istanbul.  相似文献   

18.
Dodecylammonium bentonite (DB) and dodecylammonium sepiolite (DS) were used as sorbents for phenoxyalkanoic acid herbicides 2,4‐D ((2,4‐dichlorophenoxy)acetic acid), 2,4‐DP ((RS)‐2‐(2,4‐dichlorophenoxy)propionic acid), 2,4‐DB (4‐(2,4‐dichlorophenoxy)butyric acid), 2,4,5‐T ((2,4,5‐trichlorophenoxy)acetic acid), and MCPA ((4‐chloro‐2‐methylphenoxy)acetic acid). Langmuir, Freundlich, and the linear Henry’s Law isotherm adsorption parameters were calculated from the adsorption isotherms. Langmuir equation showed poor fit for both adsorbents. According to the evaluation using the Freundlich equation, the DS sample showed much higher and stronger sorption capacity than DB. Similar behaviour was also observed in the case of the linear Henry’s Law isotherm. The adsorption of the herbicides on both DB and DS decreased in the order of 2,4‐DB > 2,4,5‐T > 2,4‐DP > 2,4‐D > MCPA.  相似文献   

19.
The use of in‐field analysis of vapor‐phase samples to provide real‐time volatile organic compound (VOC) concentrations in groundwater has the potential to streamline monitoring by simplifying the sample collection and analysis process. A field validation program was completed to (1) evaluate methods for collection of vapor samples from monitoring wells and (2) evaluate the accuracy and precision of field‐portable instruments for the analysis of vapor‐phase samples. The field program evaluated three vapor‐phase sample collection methods: (1) headspace samples from two locations within the well, (2) passive vapor diffusion (PVD) samplers placed at the screened interval of the well, and (3) field vapor headspace analysis of groundwater samples. Two types of instruments were tested: a field‐portable gas chromatograph (GC) and a photoionization detector (PID). Field GC analysis of PVD samples showed no bias and good correlation to laboratory analysis of groundwater collected by low‐flow sampling (slope = 0.96, R2 = 0.85) and laboratory analysis of passive water diffusion bag samples from the well screen (slope = 1.03; R2 = 0.96). Field GC analysis of well headspace samples, either from the upper portion of the well or at the water‐vapor interface, resulted in higher variability and much poorer correlation (consistently biased low) relative to laboratory analysis of groundwater samples collected by low‐flow sample or passive diffusion bags (PDBs) (slope = 0.69 to 0.76; R2 = 0.60 to 0.64). These results indicate that field analysis of vapor‐phase samples can be used to obtain accurate measurements of VOC concentrations in groundwater. However, vapor samples collected from the well headspace were not in equilibrium with water collected from the well screen. Instead, PVD samplers placed in the screened interval represent the most promising approach for field‐based measurement of groundwater concentrations using vapor monitoring techniques and will be the focus of further field testing.  相似文献   

20.
In India, the annual production of tea is ca. 857,000 tonnes, which is 27.4% of the total world production. The amount of tea factory waste (TFW) produced per annum after processing is ca. 190,400 tonnes. TFW can be used as a low cost adsorbent for the removal of toxic metals from the aqueous phase. An investigation was carried out to study the feasibility of the use of TFW as an adsorbent for the removal of the heavy metal, zinc. Equilibrium, kinetic and thermodynamic studies were reported. The straight line plot of log (qeq) versus time t for the adsorption of zinc shows the validity of the Lagergren equation. The various steps involved in adsorbate transport from the solution to the surface of the adsorbent particles were dealt with by using a Weber‐Morris plot, qe versus t0.5 for the TFW. The rate controlling parameters, kid,1 and kid,2, were determined and it was found that the macro‐pore diffusion rate was much larger than micro‐pore diffusion rate. A batch sorption model, which assumes the pseudo‐second‐order mechanism, was used to predict the rate constant of sorption, the equilibrium sorption capacity and the initial sorption rate with the effect of initial zinc (II) ion concentration. Equilibrium data obtained from the experiments were analyzed with various isotherms, i. e., Freundlich, Langmuir, Redlich‐Peterson and Tempkin. The adsorption equilibrium was reached in 30 min and the adsorption data fitted well to all models. The maximum adsorption capacity of TFW for zinc (II) ions was determined to be 14.2 mg/g. The capacity of adsorption on Zn(II) increased with increasing temperatures and pH. The maximum uptake level of zinc was observed at pH of 4.2. The various thermodynamic parameters, i. e., ΔG°, ΔH° and ΔS°, were estimated. The thermodynamics of the zinc ion/TFW system indicated a spontaneous, endothermic and random nature of the process. The results showed that the TFW, which has low economical value, is a suitable adsorbent for the removal of zinc (II) ions from aqueous solutions.  相似文献   

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