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1.
This study evaluates the performance of two low cost and high performance adsorption materials, i.e., activated carbon produced from two natural waste products: Bamboo and coconut shell, in the removal of three pesticides from drinking water sources. Due to the fact that bamboo and coconut shell are abundant and inexpensive materials in many parts of the world, they respond to the “low‐cost” aspect. The adsorption capacities of two local adsorbents have been compared with commercial activated carbon to explore their potential to respond to the “high quality” aspect. Two pesticides were selected, namely dieldrin and chlorpyrifos, because they are commonly used in agriculture activities, and may remain in high concentrations in surface water used as drinking water sources. The results indicate that the adsorption of pesticides on activated carbons is influenced by physico‐chemical properties of the activated carbon and the pesticides such as the presence of an aromatic ring, and their molar mass. The activated carbon produced from bamboo can be employed as low‐cost and high performance adsorbent, alternative to commercial activated carbon for the removal of pesticides during drinking water production. The performance of activated carbon from bamboo was better due to its relatively large macroporosity and planar surface. The effect of adsorbent and pesticide characteristics on the performance was derived from batch experiments in which the adsorption behavior was studied on the basis of Freundlich isotherms.  相似文献   

2.
Batch and continuous flow adsorption experiments are carried out and the design of a full‐scale facility for removing dissolved natural organic matter (DNOM) from Catalan Lakewater is demonstrated. The adsorption efficiency is proportional to the temperature and the amount of adsorbent unlike pH increase. The highest DNOM removal rate is obtained at 35 °C, pH 4, and an adsorbent amount of 0.8 g L?1. Optimum contact time for batch studies is 60 min at equilibrium. Correlation constants (r) of Langmuir and Freundlich isotherms are 0.8905 and 0.9739, respectively. Based on the Freundlich isotherm, the highest adsorption capacity (qmax) obtained is 2.44 and 6.01 mg DNOM/g granulated activated carbon (GAC) for raw and enriched water, respectively. Consequently, the effects of adsorbent amount, bed depth, empty bed contact time, and organic loading on removal performance are investigated in the rapid small‐scale column test (RSSCT) columns. The targeted effluent concentration of 1 mg DNOM/L can easily be achieved in the columns. At the design capacity of the facility, 15 adsorption columns with dimensions of 7 m height, 4.33 m diameter, and 22 days of operation cycle are required to remove DNOM from raw water.  相似文献   

3.
The adsorption of Cu(II) onto HCl treated rubber leaf powder (HHBL) was investigated in batch and column studies. The adsorbent was characterized by spectroscopic and quantitative analyses in order to understand the mechanism of copper adsorption. HHBL is mesoporous in nature as indicated by Bruneuer, Emmett and Teller (BET) analysis, and has various kinds of functional groups such as Si‐OH, ROH, RCOOH, RCOO, RNH2, C‐O‐C and aromatic rings as detected by Fourier transform infrared (FTIR) spectroscopy. Copper adsorption was confirmed by scanning electron microscopy (SEM) and energy dispersive X‐ray spectroscopy (EDS). The equilibrium process was described well by the Langmuir isotherm model, and a maximum adsorption capacity of 8.39 mg/g was recorded for the smallest adsorbent size (<180 μm). The two main adsorption mechanisms involved were ion exchange and complexation. The fixed bed column study demonstrated satisfactory applicability of HHBL in removing Cu(II) from aqueous solutions.  相似文献   

4.
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   

5.
Bioremediation is intensively studied today as a treatment method for soil contaminated with chlorinated pesticides, chemicals counted among persistent organic pollutants. In the presented work, results of desorption kinetics study using consecutive Tenax TA solid phase extraction (SPE) were tested as predictors of 3‐wk anaerobic soil bioremediation effectiveness for chlorinated pesticides γ‐HCH, DDT, and methoxychlor. Field‐contaminated samples were used in these experiments, and conditions of bioremediation tests were based on previous research. Amounts of pesticides removed during bioremediation (43–98% of initial concentrations) were in most cases much larger (average ratio 1.37) than rapidly desorbing fractions estimated in SPE using two‐compartment model of desorption kinetics. The scatter of results was also considerable (standard deviation 0.45). However, there was a statistically significant correlation between amounts removed and rapidly desorbing fractions (R2 = 0.64), indicating a relationship between degradability and desorbability. Nonetheless, determination of rapidly desorbing fractions was considered rather a poor indicator of soil bioremediation efficiency for chlorinated pesticides. The total amounts of pesticides desorbed by Tenax in 72 h performed better in this respect (R2 = 0.73, fraction removed/desorbed = 1.10 ± 0.20, average ± standard deviation). Disappearance of DDT during bioremediation was accompanied by DDD formation but this was considerably lower than results expected from stoichiometry.  相似文献   

6.
The adsorption of Ni(II) from aqueous solutions using base treated cogon grass or Imperata cylindrica (NHIC) was performed under batch and column modes. Batch experiments were conducted to determine the factors affecting adsorption such as pH, adsorbent dosage, initial nickel concentration, contact time and temperature. The fixed‐bed column experiment was performed to determine the practical applicability of NHIC and to obtain the breakthrough curve. Adsorption was fast as equilibrium was achieved within 60 min, and was best described by the pseudo second order model. According to the Langmuir model, a maximum adsorption capacity of 6.96 mg/g was observed at pH 5 and at a temperature of 313 K. Thermodynamic parameters such as ΔG0, ΔH0 and ΔS0 were calculated, and indicated that adsorption was a spontaneous and endothermic process. The mechanistic pathway of Ni(II) uptake was examined by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and energy dispersive X‐ray (EDX) spectroscopy. The Thomas and Yoon‐Nelson models were used to analyze the fixed‐bed column data.  相似文献   

7.
The adsorption of three cationic dyes (rhodamine B, RB; crystal violet, CV; and malachite green, MG) onto termite feces, a low‐cost adsorbent, was investigated. The adsorbent was characterized by IR spectroscopy, point of zero charge measurement, and the Boehm titration method. The adsorption follows the pseudo‐second‐order kinetic model and the Langmuir–Freundlich isotherm with maximum adsorption capacities of 95.53 mg g?1 (RB), 75.71 mg g?1 (CV), and 44.78 mg g?1 (MG). The study of thermodynamics showed that the adsorption is a spontaneous and endothermic process. This works suggest that termite feces can be used as a new low‐cost adsorbent for cationic dye removal.  相似文献   

8.
This work describes the potential usability of neutralized red mud for the removal of organochlorine pesticides (OCPs) from aqueous solutions. After examination on the adsorption capability of neutralized red mud for all studied OCPs, the experiments were performed by employing aldrin as a model compound. The effect of several parameters, such as contact time, pH of the solution, initial aldrin concentration, and dosage of the adsorbent was evaluated by batch experiments. The determination of OCPs was carried out using traditional liquid–liquid extraction followed by a GC coupled with µ‐electron capture detector (GC‐µECD). The results showed that adsorption equilibrium time depended upon the initial aldrin concentration and adsorption followed the second‐order kinetic model. Kinetic study also indicated that the film diffusion mechanism was a main rate control mechanism. The removal was explained by considering the electrostatic interactions between metal oxides surface of the neutralized red mud and inductively charged centers (negative charge (d?) of chlorine atoms and positive charge (d+) of π‐cloud aromatic ring) of the aldrin molecules. In comparison to the Langmuir isotherm model, the Freundlich model better represented the adsorption data. The neutralized red mud was also succesfully employed for the removal of OCPs from real water samples, including tap water and surface (lake) water, fortified with studied OCPs.  相似文献   

9.
The potential of MCM‐41 for the removal of cationic dyes from water solution was evaluated using sodium dodecyl sulfate (SDS) for the surface modification of this mesoporous material. Admicelle structures formed on the surface of the calcined MCM‐41 are capable of removing organic pollutants and cationic species from water environment. The structural, textural, and surface chemical characteristics of the prepared SDS‐modified MCM‐41 (SDS‐MCM‐41) were studied. The adsorption capacity of SDS‐MCM‐41 was evaluated for methylene blue (MB) as a target cationic dye. Equilibrium adsorption isotherm data were manipulated employing nonlinear regression analysis. The Langmuir, Freundlich, and Sips isotherm models were examined. The adsorption data were well fitted to both Langmuir and Sips isotherm models. The maximum adsorption capacity of SDS‐MCM‐41 for MB, based on Langmuir and Sips models, were 290.8 and 297.3 mg g?1, respectively. Ethanol was found to be an effective solvent for partial regeneration of the adsorbent.  相似文献   

10.
In the current study the application of organo‐modified bentonite for the adsorption of mycotoxins (aflatoxin B1, citrinin, patulin, and zearalenone) is presented. The modification of clays is carried out using benzyl‐tri‐n‐butyl ammonium bromide (BTB), benzethonium chloride (BTC), and dioctyl sodium sulfosuccinate (DSS). Various experimental parameters such as pH, time, adsorbent dose, and mycotoxins concentration are thoroughly studied. The modified clays (B‐BTB, B‐BTC and B‐DSS) are characterized by X‐ray fluorescence, X‐ray diffraction, and Fourier transform infrared spectroscopy. The results depicted the high detoxification efficiency (≈99%) of modified clays for the removal of mycotoxins under optimized conditions (pH 5, time: 30 min, adsorbent amount: 50 mg). The adsorption capacities of modified clays are found in the order of: B‐BTC (AFB1: 18.02, CIT: 18.35, PAT: 18.21, ZEA: 18.09 mg g?1) > B‐BTB (AFB1: 17.7, CIT: 18.11, PAT: 17.95, ZEA: 17.90 mg g?1) > B‐DSS (AFB1: 17.5, CIT: 18.02, PAT: 17.86, ZEA: 17.80 mg g?1). The obtained results fitted well with thermodynamic, isothermal (Langmuir) and pseudo‐second order kinetics. Low cost organo‐modified bentonite shows the promise in mitigating mycotoxin contamination, which could improve food safety and reduce environmental contamination.  相似文献   

11.
The adsorption kinetics of carbamazepine, naproxen, and trimethoprim in aqueous solution by Amberlite? XAD‐7 has been studied. The influence of adsorbent dose (1–3 g/L), stirring rate (80–240 rpm), pH (2–9), temperature (20–60°C), and initial concentration (25–75 ppm) on the adsorption kinetics has been analyzed. The removal efficiency in the first 2 h reaches 85% for carbamazepine, 60% for naproxen, and 70% for trimethoprim. pH appears to be the most important factor conditioning the removal of these latter solutes, whereas carbamazepine adsorption seems to be independent of the pH of the adsorptive solution. Initial concentration and operation temperature moderately influence the adsorption process. Finally, stirring rate scarcely affects the process. The experimental data have been fitted to four kinetic models, namely pseudo‐first and pseudo‐second order, intra‐particle diffusion and Bangham's. The model providing the best fit is the pseudo‐second order one. Again, pH is the factor that affects the adsorption rate in a more remarkable manner although other parameters such as temperature and stirring rate also contribute to accelerate the removal of the solutes. Under the optimal operation conditions, Amberlite? XAD‐7 exhibits a promising ability for the removal of the pharmaceuticals under study.  相似文献   

12.
A simple and rapid soft‐templating coupled with one‐pot solvent thermal method is developed to synthesize S‐doped magnetic mesoporous carbon (S‐doped MMC). In this method, phenolic resin is used as a carbon precursor and Pluronic copolymer P123 is used as a template and 2,5‐dimercapto‐1,3,4‐thiadiazole is used as sulfur source. Prepared S‐doped MMC processes a high specific surface area, the Fe3O4 particles are well embedded in the mesoporous carbon walls that exhibit a strong magnetic response, and the hydrated iron nitrate loading amount of 0.808 g is the best. Batch adsorption experiments are carried out at different pH, initial concentration, temperature, and contact time on the adsorption of methyl orange (MO) by S‐doped MMC. The kinetic data of the adsorption process are better fitted with pseudo‐second‐order model than the pseudo‐first‐order model. Langmuir model is more suitable for the equilibrium data than Freundlich model. The thermodynamic parameters including ΔG0, ΔH0, and ΔS0 indicate that the adsorption is a feasible, spontaneous, and endothermic process. Finally, it is found that the coexistence of PO43?, NO3?, SO42?, Cl?, and CO32? does not influence the adsorption process. These results illustrate S‐doped MMC can be an efficient adsorbent for the removal of MO from wastewater.  相似文献   

13.
The chlorohydrocarbon pesticides (CHPs) (principally DDT, dieldrin, hexachlorocyclohexane (HCH) including lindane, chlordane, heptachlor and heptachlorepoxide, aldrin and hexachlorobenzene (HCB)) were used extensively in Australia during the 1960s and 1970s. These were progressively banned from the 1970s with DDT being totally banned in 1987. The levels in marine waters are believed to have progressively declined as indicated by water in the Brisbane River, which consistently fell from maximum concentrations of about 1.7 μg/l in 1972–1973 to not detectable in 1986–1987. In some urban areas sediment concentrations, up to 1700 μg/kg dry weight, were recorded in the early 1990s which may reflect the reworking and exposure of older more contaminated material. Fish exhibited consistent occurrence of DDT, HCH, dieldrin and HCB through the 1970s to the 1990s. Maximum concentrations of DDT and dieldrin occurred generally in the 1970s at 40.3 and 8.8 μg/g wet weight, and minimums in the 1990s at 2.4 and 0.041 μg/g wet weight respectively. Inputs of dialdrin from sewage and DDT from the broad environment, reflected by the calculated daily human uptake in the diet, were shown to decline with half-lives of 1.1–1.5 and about 3 years respectively. This evidence suggests that banning of the CHPs has greatly reduced the inputs into the marine environment with consequent reductions in concentrations in biota but there is the occasional occurrence of relatively high concentrations.  相似文献   

14.
Burial characteristics and risks associated with 13 organochlorine pesticides (OCPs; α-HCH, β-HCH, γ-HCH, δ-HCH, p,p′-DDE, p,p′-DDD, p,p′-DDT, heptachlor, aldrin, dieldrin, endrin, α-endosulfan and β-endosulfan) in core sediments of Lake Baiyangdian were investigated. The core sediments were taken from areas of different anthropogenic activity along the lake. Concentrations of hexachlorocyclohexane (HCH), dichlorodiphenyltrichloroethane (DDT), heptachlor, aldrin, and endosulfan ranged from 0.64 to 2.72, nd (undetectable levels) to 2.79, 0.29 to 1.37, nd to 2.62, and nd to 1.76 ng g?1, respectively. Concentrations of OCPs in the core sediments exhibited the following spatial trend: Dongtianzhuang > Shaochedian > Zaolinzhuang. Concentrations in the surficial layer were also found to be greater than those in the bottom layer. OCPs were dominated by HCH. β-HCH was found in the greatest concentrations, indicating that the majority of HCH came from older inputs to the area. The ratio of DDT and its metabolites (DDD and DDE) also suggested a lack of recent inputs to the lake environment. The residues of heptachlor, aldrin, and endosulfan in core sediments indicated that cyclodienes were historically applied in the area. The OCP risk assessment, which was based on effect range low and threshold effect level values, suggested that the top layer of sediment in Dongtianzhuang cores had a relatively high toxicity to human health and the environment.  相似文献   

15.
In this work, 8‐hydroxyquinoline is used as the active sites in cross‐linked chitosan beads with epichlorohydrin (CT‐8HQ). The CT‐8HQ material was shaped in bead form and used for heavy metal removal from aqueous solution. The study was carried out at pH 5.0 with both batch and column methods and the maximum adsorption capacity of metal ions by the CT‐8HQ was attained in 4 h in the batch experiment. The adsorption capacity order was: Cu2+ > Ni2+ > Zn2+ for both mono‐ and multi‐component systems with batch conditions. From breakthrough curves with column conditions, the adsorption capacity followed the order Cu2+ > Zn2+ > Ni2+ for both mono‐ and multi‐component systems. The CT‐8HQ beads maintained good metal adsorption capacity for all five cycles with absorbent restoration achieved with the use of 1.0 mol L–1 HCl solution, with 90% regeneration.  相似文献   

16.
In this study, crude multi‐walled carbon nanotubes (MWCNT) was functionalized by a two‐step process; first using strong mixed acids (H2SO4/HNO3) and then treatment with 1,3‐phenylenediamine (mPDA). The equilibrium adsorption of CO2 on pristine MWCNT and amine functionalized MWCNT (MWCNT‐NH2) were investigated. Experiments were preformed via application of volumetric method in a dual sorption vessel at temperature range of 298–318 K and pressures up to 40 bars. The results obtained indicated that the equilibrium uptake of CO2 increased after functionalizing of MWCNT. The increase in CO2 capture by MWCNT‐NH2 was attributed to the existence of great affinity between CO2 molecules and amine sites on this adsorbent at low pressures. The experimental data were analyzed by means of Freundlich and Langmuir adsorption isotherm models. The data obtained revealed a fast kinetics for the adsorption of CO2 in which most of adsorption occurred at initial period of adsorption experiments. This renders MWCNT as a suitable adsorbent for practical applications. Values of isosteric heat of adsorption were evaluated based on Clausius–Clapeyron equation. The results demonstrated that both chemisorption and physisorption played important role in CO2 adsorption on MWCNT‐NH2, whereas the physisorption process was dominant for CO2 adsorption on MWCNT.  相似文献   

17.
A pioneering investigation of semi‐volatile organic compounds (SVOCs) in shallow groundwater in China was hereby reported. Representative groundwater samples were collected from three selected regions: Eastern Hai River Plain, Yangtze River Delta, and Yunnan‐Guizhou Plateau, and analyzed for 103 SVOCs linked to agricultural and industrial practices. Analytical results showed that 70 of the 103 SVOCs were present in the groundwater samples, a detection frequency of approximately 86%. Compounds detected most frequently included P,P′‐DDT (53.49%, MDL 0.0007 µg/L), 2,4‐dinitrotoluene (51.16%, MDL 0.02 µg/L), and phenol (51.16%, MDL 0.02 µg/L). Fifteen SVOCs, such as P,P′‐DDT, 2,4‐dinitrotoluene, heptachlor, and aldrin, were detected at concentrations exceeding the USA National Recommended Water Quality Criteria‐2009 (USNRWQC‐2009). Most of these 15 SVOCs belong to polycyclic aromatic hydrocarbons and organochlorine pesticides. The detection of SVOCs in the Yunnan‐Guizhou Plateau warrants special concern, since this region has limited human activities and been assumed as an environmentally pristine area. The data from this work are expected to contribute to the database of contemporary groundwater quality in China.  相似文献   

18.
19.
Polychlorinated biphenyls (PCBs) and organochlorine (OC) pesticide levels were determined in blubber samples collected from stranded and incidentally by-caught Hector’s (Cephalorhynchus hectori hectori) and Maui’s (Cephalorhynchus hectori maui) dolphins from New Zealand waters between 1997 and 2009. PCBs (45 congeners) and a range of OC pesticides including dieldrin, hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT), along with its metabolites DDE and DDD were determined. OC pesticides dieldrin, p,p′-DDE, p,p′-DDD and p,p′-DDT were present at the highest concentrations. Sum DDT concentrations ranged from 93.7 to 8210 (Mean = 1358, S.D = 1974) and 252.4 to 57,390 (Mean = 12,389, S.D = 18,161) μg/kg wet weight in females and males, respectively. Similarly, Σ45CB concentrations ranged from 45.5 to 981.3 (Mean = 333.2, S.D = 265.8) and 60.5 to 5574 (Mean = 1833, S.D = 1659) μg/kg wet weight in females and males, respectively. The transfer of ΣDDTs and summed PCBs (both as ΣICES7CBs and Σ45CBs) between a pregnant female and her unborn fetus was calculated at 5.7% and 4.3%, respectively. As the fetus was close to term, this likely represents the degree of placental transfer. Concentrations of OC pesticides determined in the present study are higher than those previously reported for Hector’s dolphins. Sum DDT and DDE/ΣDDT levels calculated reveal New Zealand’s legacy of DDT usage, particularly off the east coast of the South Island.  相似文献   

20.
Batch kinetic studies were carried out for the removal of safranin from aqueous solution using a biomatrix prepared from rice husk. The adsorption kinetic data were modeled using the pseudo‐first‐order and pseudo‐second‐order kinetic equations. The linear and non‐linear forms of these two widely used kinetic models were compared in this study. In order to determine the best‐fitting equation, the coefficient of determination (r2), the sum of the squares of the errors (SSE), sum of the absolute errors (SAE), average relative error (ARE), hybrid fractional error function (HYBRID), Marquardt's percent standard deviation (MPSD), and the Chi‐squared test (χ2) were used as error analysis methods. Results showed that the non‐linear forms of pseudo‐first‐order and pseudo‐second‐order models were more suitable than the linear forms for fitting the experimental data. Non‐linear method is thus more appropriate for estimating the kinetic parameters and should primarily be used to describe adsorption kinetics.  相似文献   

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