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1.
Adsorption and desorption of 137Cs by acid sulphate soils from the Nakhon Nayok province, South Central Plain of Thailand located near the Ongkarak Nuclear Research Center (ONRC) were investigated using a batch equilibration technique. The influence of added limestone (12 and 18 tons ha?1) on 137Cs adsorption–desorption was studied. Based on Freundlich isotherms, both adsorption and desorption of 137Cs were nonlinear. A large portion (98.26–99.97%) of added 137Cs (3.7?×?103?7.03?×?105 Bq l?1) was sorbed by the soils with or without added lime. The higher lime treatments, however, favoured stronger adsorption of 137Cs as compared with soil with no lime, which was supported by higher K ads values. The addition of lime, the cation exchange capacity and pH of the soil increased and hence favoured the stronger adsorption of 137Cs. Acid sulphate soils with a high clay content, medium to high organic matter, high CEC, and predominant clay types consisting of a mixture of illite, kaolinite, and montmorillonite were the main soil factors contributing to the high 137Cs adsorption capacity. Competing cations such as NH4 +, K+, Na+, Ca2+, and Mg2+ had little influence on 137Cs adsorption as compared with liming, where a significant positive correlation between K ads and soil pH was observed. The 137Cs adsorption–desorption characteristics of the acid sulphate soils studied exhibited a very strong irreversible sorption pattern. Only a small portion (0.09–0.58%) of 137Cs adsorbed at the highest added initial 137Cs concentration was desorbed by four successive soil extractions. Results clearly demonstrated that Nakhon Nayok province acid sulphate soils have a high 137Cs adsorption capacity, which limits the 137Cs bioavailability.  相似文献   

2.
采用批吸附室内模拟实验研究了雄烯二酮在我国红壤、潮土、黑土3种典型土壤中的吸附特征,以及牛粪溶解态有机质(DOM)对土壤吸附雄烯二酮的影响。结果表明,雄烯二酮在土壤中吸附动力学符合Elovch方程(R20.89),热力学特征可通过Freundlich等温吸附方程(R20.83)描述,土壤对雄烯二酮的吸附呈非线性吸附特征,其中潮土吸附等温线的非线性最强(n=0.37);吸附系数K f介于6.0~20.2,并与有机质含量呈显著正相关(p0.05)。雄烯二酮浓度较低时,共存牛粪DOM抑制其在土壤表面的吸附作用。研究认为,有机质是土壤吸附雄烯二酮的主要组分,共存牛粪DOM可促进雄烯二酮向地表水和地下水的迁移。  相似文献   

3.
The bioavailability of arsenic (As) in the soil environment is largely governed by its adsorption–desorption reactions with soil constituents. We have investigated the sorption–desorption behaviour of As in four typical Bangladeshi soils subjected to irrigation with As-contaminated groundwater. The total As content of soils (160 samples) from the Laksham district ranged from <0.03 to approximately 43 mg kg−1. Despite the low total soil As content, the concentration of As in the pore water of soils freshly irrigated with As-contaminated groundwater ranged from 0.01 to 0.1 mg l−1. However, when these soils were allowed to dry, the concentration of As released in the pore water decreased to undetectable levels. Remoistening of soils to field moisture over a 10-day period resulted in a significant (up to 0.06 mg l−1) release of As in the pore water of soils containing >10 mg As kg−1 soil, indicating the potential availability of As. In soils containing <5 mg As kg−1, As was not detected in the pore water. A comparison of Bangladeshi soils with strongly weathered long-term As-contaminated soils from Queensland, Australia showed a much greater release of As in water extracts from the Australian soils. However, this was attributed to the much higher loading of As in these Australian soils. The correlation of pore water As with other inorganic ions (P, S) showed a strongly significant (P < 0.001) relationship with P, although there was no significant relationship between As and other inorganic cations, such as Fe and Mn. Batch sorption studies showed an appreciable capacity for both AsV and AsIII sorption, with AsV being retained in much greater concentrations than AsIII.  相似文献   

4.
A novel extraction method was established to determine the water-extractable (available) content of sulfamethoxazole (SMX) in soil. The SMX imprinted polymers (MIPs) were synthesised and the performance was evaluated by Fourier transform infrared spectroscopy, scanning electron microscopy and binding experiments. Results showed that the MIPs exhibited good selectivity for SMX, so the MIPs were applied as a sorbent. SMX in soil was extracted by water, sorbed from the extract to MIPs and analysed with a high performance liquid chromatography (HPLC) after its desorption from MIPs. Meanwhile, the classic organic solvent extraction was employed to measure the total SMX content in soil. Results showed that when SMX level in spiked soils varying from 1.0–500?μg?kg?1, the observed recoveries of available SMX contents ranged from 63.27?±?3.11% to 82.11?±?2.77% (n?=?3), while the total SMX varied between 89.59?±?1.65% and 97.64?±?3.92% (n?=?3). The detection limit of the developed method for SMX in soils was 0.05?μg?kg?1. Available SMX contents in five field soil samples ranged from 0.13 to 4.14?μg?kg?1, which were only 0.35–25.40% of the respective total SMX contents. Results from this study manifest the importance of the extents of SMX immobilisation with different soils for assessing SMX's ecological and human health risks.  相似文献   

5.
Sorption characteristics of the Benzimidazole fungicide Carbendazim were assessed in seven different soils using batch equilibrium method and analysed by UV-Vis spectrophotometer. The values of adsorption co-efficient Kd ranged from 14.3 to 39.8?µg/mL depending upon unique physiochemical properties of soils. Negative values for Gibbs free energy (ΔG) proposed an exothermic and low interaction between Carbendazim and soil samples leading to physiosorption. Statistical analysis showed a negative correlation of soil pH and Kd (R2= ?0.80) and a positive correlation with organic matter (R2?=?0.77). Activated carbon prepared from Arachis hypogaea (peanut shells) by acid activation for Carbendazim removal from soils was characterised by FTIR spectrometry, indicating the change in functional groups. The highest percentage removal observed was 70% in 5?ppm initial Carbendazim concentration while 65% in 7.5?ppm concentration. This method can be implied in agricultural soils as an efficient and cheap technique for removing the hazardous pesticides from the environment.  相似文献   

6.
This study was designed to evaluate the adsorption‐desorption hysteresis of endosulfan (1,2,3,4, 7,7‐hexachlorobicyclo[2,2,1]‐2‐heptene‐5,6‐bisoxymethylene sulfite) in selected tropical soils. Two major tropical soils from Thailand were selected, Rangsit lowland soils (Rangsit series) and Phrabat upland soils (Pakchong series). The soil types were sub‐divided into plow soils, 0–20cm depth from the surface, and subsoils, 20–40cm depth. Adsorption was determined in 24h batch equilibrium, with five different concentrations of 14C endosulfan ranging from 1.04 to 16.64 ng/mg soils. Four successive desorption studies were performed continuously after three adsorption concentrations, 24h for each successive. Adsorption coefficient values (K ads) as determined by Freundlich model ranged from 0.02 to 0.14 and found to be higher in Rangsit soils as expected when compared with Phrabat soils. Desorption was hysteresis in every desorption study. Desorption coefficient values (K des) were higher than adsorption (K des).  相似文献   

7.
邵兴华  张建忠  王艾平 《生态环境》2010,19(10):2355-2359
采用室内培养法研究了淹水对2种酸性红壤(旱地红壤、水稻土)磷吸附解吸特性及草酸可提取态P的影响。淹水培养实验中,2种土壤分别淹水0(对照),1、2、3、4、8周,淹水培养结束后进行P吸附解吸实验,解吸实验结束后测定土样中草酸可提取态P。结果表明:与氧化状态相比,淹水后旱地红壤P吸附量减少,水稻土淹水1、2、3周P吸附量高于氧化状态,继续淹水4和8周后P吸附量减少。淹水前后旱地红壤P吸附量均大于水稻土。用简单Langmuir方程拟合P等温吸附曲线,除淹水4周外,P最大缓冲容量(MBC)随淹水时间延长而降低。结合能常数(K)淹水前后的变化规律性差。2种土壤P解吸量随加入P量增加而增加。氧化、还原状态下,2种土壤酸性草酸铵可提取P均远远大于CaCl2解吸P,虽然水稻土吸附P量低于旱地红壤,但P解吸量无论是CaCl2解吸P还是酸性草酸铵可提取P均大于旱地红壤,主要原因在于水稻土全P及速效P含量大于旱地红壤。淹水后草酸可提取态P增加,吸附P的释放和被新近形成的铁氧化物再吸附是淹水后草酸可提取态P增加的主要原因。  相似文献   

8.
9.
Jurassic ironstones outcropping over parts of eastern England give rise to soils with arsenic concentrations in excess of the UK soil guideline value of 20 mg kg−1 for residential areas. Total arsenic concentrations were determined for 73 ironstone derived soils and bioaccessible arsenic determined using an in vitro physiologically based extraction test. The bioaccessible arsenic concentration for these soils was found to be well below the soil guideline value with a mean concentration of 4 mg kg−1 and a range of 2–17 mg kg−1. The bioaccessible fraction ranges from 1.2 to 33%. Data from a sequential extraction test based on the use of aqua regia as the main extractant is presented for a subset of 20 of the soils. Chemometric data reduction is used to demonstrate that the bioaccessible arsenic is mainly contained within calcium iron carbonate (sideritic) assemblages and only partially iron aluminosilicates, probably berthierine, and iron oxyhydroxide phases, probably goethite. It is suggested that the bulk of the non-bioaccessible arsenic is bound up with less reactive iron oxide phases.  相似文献   

10.
Liming materials have been used to immobilize heavy metals in contaminated soils. However, no studies have evaluated the use of eggshell waste as a source of calcium carbonate (CaCO?) to immobilize both cadmium (Cd) and lead (Pb) in soils. This study was conducted to evaluate the effectiveness of eggshell waste on the immobilization of Cd and Pb and to determine the metal availability following various single extraction techniques. Incubation experiments were conducted by mixing 0-5% powdered eggshell waste and curing the soil (1,246 mg Pb kg?1 soil and 17 mg Cd kg?1 soil) for 30 days. Five extractants, 0.01 M calcium chloride (CaCl?), 1 M CaCl?, 0.1 M hydrochloric acid (HCl), 0.43 M acetic acid (CH?COOH), and 0.05 M ethylendiaminetetraacetic acid (EDTA), were used to determine the extractability of Cd and Pb following treatments with CaCO? and eggshell waste. Generally, the extractability of Cd and Pb in the soils decreased in response to treatments with CaCO? and eggshell waste, regardless of extractant. Using CaCl? extraction, the lowest Cd concentration was achieved upon both CaCO? and eggshell waste treatments, while the lowest Pb concentration was observed using HCl extraction. The highest amount of immobilized Cd and Pb was extracted by CH?COOH or EDTA in soils treated with CaCO? and eggshell waste, indicating that remobilization of Cd and Pb may occur under acidic conditions. Based on the findings obtained, eggshell waste can be used as an alternative to CaCO? for the immobilization of heavy metals in soils.  相似文献   

11.
This study was conducted to examine adsorption of pesticides bifenthrin, carbosulfan, λ-cyhalothrin, cypermethrin, endosulfan, parathion methyl, monocrotophos and 4-nitrophenol by sandy clay loam (S.C.L) and sandy loam (S.L) soils (with varying organic content). There was no significant difference between the observed soil water partitioning coefficient values (K d) derived from linear and nonlinear Freundlich isotherms. Adsorption of pesticides on S.C.L soils was higher than those on S.L soils. K d values showed significant correlations (r 2?=?0.8???0.99 and 0.65???0.97) with soil organic carbon content (OC) and weak correlations (r 2?=?0.2???0.29 and 0.1???0.18) with clay contents of S.C.L and S.L soil at p?≤?0.05, respectively for all pesticides (except monocrotophos). Observed K oc values (soil-water partitioning constants based on the organic C fraction of the soil) were in accordance with the literature values of Wauchope and Tomlin with a maximum deviation of less than 0.5 log units. Ten Quantitative Property-Property Relationships (QPPR) among water solubility, n-octanol water coefficient (K ow) and K oc were proposed for studied pesticides except monocrotophos. The models were considered acceptable when predicted-observed difference for log?K ow and log?K oc were ≤?0.3 and ≤?0.5?log units, respectively, during the validation procedure. This work indicates that the log?K oc derived from the log Kow, from some of existing relationships, may be a fair predictor where observed values (i.e., K d and K oc) are not available. Furthermore, predicted leaching potential by groundwater ubiquity scores (GUS) equation was solved by using observed K oc values and literature reported half lives of pesticides. GUS ranked the mobility of nonvolatile compounds i.e., bifenthrin, λ-cyhalothrin, cypermethrin and endosulfan extremely low; methyl parathion very low; 4-nitrophenol low; carbofuran and monocrotophos very high in S.C.L and S.L soils, respectively. Results discussed in this paper provide background to prioritize pesticides or chemical groups that should be evaluated under field conditions with regard to their leaching potential to groundwater in arid climates.  相似文献   

12.
The level of accumulation of selected essential and non-essential metals, namely; Ca, Cu, Fe, Zn, Mn, Cd, Pb, and Cr have been investigated in the seeds, fruits, and flowers of some medicinal plants utilized for tapeworm treatment in Ethiopia and their respective soil samples. These include seed of Cucurbita maxima (Duba), fruit of Embelia abyssinica (Ankoko), flowers of Hagenia abyssinica (Kosso), and fruits of Rosa abyssinica (Kega) and their respective soil samples. A wet digestion procedure with a mixture of conc. HNO3 and HClO4 for the plant samples and a mixture of conc. HNO3, HCl, and H2O2 for soil samples were used to solubilize the metals. Ca (1280–12,670?mg?kg?1) was the predominant metal followed by Fe (104–420?mg?kg?1), and Zn (18–185?mg?kg?1) in all the plant materials except for Hagenia abyssinica flower from Hirna in which Mn (16–42?mg?kg?1) followed by Fe. Among the non-essential toxic metals, Pb was not detected in Cucurbita maxima of Boji, Gedo and Hirna origins and in Rosa abyssinica of Hirna site. Similarly, Cr was not detected in Rosa abyssinica fruits of Boji and Gedo sites. The sampled soils were found to be between strongly acidic to weakly basic (pH: 4.7–7.1). In the soil samples, Ca (8528–18,900?mg?kg?1) was the most abundant metal followed by Fe (417–912?mg?kg?1), Zn (155–588?mg?kg?1), Mn (54–220?mg?kg?1), Cr (21–105. mg?kg?1), Cu (11–58?mg?kg?1), Pb (13–32?mg?kg?1) and Cd (2.8–4.8?mg?kg?1). The levels of most of the metals determined in the medicinal plants and the respective soil samples are in good agreement with those reported in the literature and the standards set for the soil by various legislative authorities.  相似文献   

13.
We studied the adsorption and desorption of two pesticides, namely isoproturon and dimetomorph, onto a model soil sample. We first show that the adsorption of isoproturon depends on pH, from 1 mg g−1 at pH 4 to 2 mg g−1 at pH 10, contrary to the adsorption of dimetomorph (5.8 mg g−1). We also studied the influence of metallic cations, copper(II), iron(III), manganese(II), and chromium(III), on the sorption of isoproturon and dimetomorph. We found that in the case of isoproturon, the presence of metallic cations does influence the retention capacity of the soil sample. The sorption becomes very weak in the presence of copper and chromium, whereas in the case of iron and manganese the sorption properties are slightly modified.  相似文献   

14.
Sorption and leaching behavior of hexaconazole in four different soils (alluvial, red, laterite, and black) was studied using a batch equilibration technique. The values of the Freundlich adsorption constant 1/nads ranged from 0.75 to 0.85 for all four soils, showing strong non-linear behavior. Upon stepwise desorption with CaCl2 solution (10 mmol·L?1), release of hexaconazole was maximum with the first elution, the amount decreasing with each subsequent one. The leaching behavior under saturated flow conditions was also studied with soil columns packed in polythene tubes. The mobility of hexaconazole was maximum in sandy loam and minimum in black soil.  相似文献   

15.
Large areas of mangroves in India are heavily disturbed by cattle grazing, hypersalinity, and other human-induced impacts. In two disturbed Avicennia marina forests and two undisturbed A. marina and Rhizophora apiculata forests in the Pichavaram mangroves of the Vellar–Coleroon estuarine complex, southeast India, we measured the rates and pathways of microbial decomposition of soil organic matter to determine if human impact is altering biogeochemical activity within these stands. Rates of total carbon oxidation (TCOX) were higher in the undisturbed A. marina forest (mean 199 mol C m–2 year–1) than in the two impacted stands (43 and 79 mol C m–2 year–1); rates of total carbon oxidation in the R. apiculata forest averaged 75 mol C m–2 year–1. Sulphate reduction (range 21–319 mmol S m–2 day–1) was the major decomposition pathway (65–85% of TCOX), except at the most disturbed forest (30% of TCOX). Rates of sulphate reduction at all sites peaked in sub-surface soils to a depth of about 1 m, leading to little carbon burial (3–5% of total C input). There was some evidence of measurable iron and manganese reduction in association with tree roots. Rates of microbial activity were rapid in comparison with rates measured in other mangrove soils, reflecting high rates of phytoplankton production and organic matter retention in this lagoon. Human-induced disturbance creates a sharp zonation of dry, hypersaline soil overlying less saline, wetter soil, suppressing surface microbial and root growth. We conclude that this vertical alteration of soil characteristics and biogeochemistry shifts the cycling of nutrients between trees and microbes to a disequilibrium state, partly explaining why mangroves are stunted in these declining forests.Communicated by G. F. Humphrey, Sydney  相似文献   

16.
The accumulation of heavy metals (HMs) in soils is potentially hazardous to human, livestock and plant species. HMs in the combined pollution soils and indigenous plants were investigated in a non-ferrous metal-smelting area. The purpose of this study was to determine the HMs in the contaminated soil and different plant species found growing on it, as well as calculation of bioaccumulation coefficients (BACs). Representative sampling sites were identified according to the land-use types. A total of 12 surface soil samples and 32 plant samples were collected. HMs were analysed by inductively coupled plasma mass spectrometry. The levels of soil pollution were assessed using Nemerow’s synthetical contamination index method. The synthetical index was in the range of 16.81–198.11. This result indicated a heavy burden on local environment. HM concentrations in plants were directly related with soil concentrations. The average BACs of five metals were found in the order of Cd (0.309)?>?Zn (0.178)?≈?Pb (0.160)?>?Cu (0.105)?>?Sb (0.0672). Spontaneous weeds including Chenopodium album Linn, Kochia scoparia and trees of Leuce, Ulmus pumila were deemed HM accumulators. The results provided a practical basis for phytoremediation of HM-contaminated soils using accumulator species.  相似文献   

17.
《毒物与环境化学》2012,94(3-6):265-280
Abstract

Sorption and desorption characteristics of glyphosate on native soil and soil amended with cow dung were investigated. Sorption was pH dependent and decreased with increasing pH. Glyphosate partition coefficient ranged from 275 to 16,200?L kg?1 in native soil, but for soil amended with cow dung it was significantly lower, viz 180–1530?L kg?1. Glyphosate partition coefficient showed strong negative correlation with cation exchange capacity and positive correlation with surface area. Phosphate in cow dung suppressed glyphosate sorption and enhanced desorption. This study revealed that cow-dung addition to soil could raise the mobility of glyphosate towards groundwater contamination due to the presence of phosphate.  相似文献   

18.
We prepared a carbonaceous sorbent for Cr(VI) from the culm of Sasa kurilensis by dehydration with concentrated H2SO4. The removal of Cr(VI) by the sorbent was highly solution pH dependent and mainly governed by physicochemical sorption. The equilibrium data fit well in the Langmuir isotherm model and indicate the endothermic nature of the Cr(VI) sorption. The desorption experiments suggest that the Cr(VI) sorption is generally irreversible, owing to strong interaction of HCrO4 with the active sites of the sorbent.  相似文献   

19.
The ability of plant species to accumulate arsenic (As) species in the biomass from As-contaminated soils is variable. Among the plants widely grown at the As-contaminated locations, Plantaginaceae and Cyperaceae families belong to the frequent ones. In this study, the ability of Plantago lanceolata (Plantaginaceae) and three wetland plant species representing the family Cyperaceae (Carex praecox, Carex vesicaria, and Scirpus sylvaticus) naturally occurring in the soils with an elevated As in the Czech Republic were investigated. The plants were cultivated under controlled conditions in an As-contaminated soil reaching 735?mg?kg?1 of the total As. The total As in plants reached up to 8.3?mg?kg?1 in leaves, and up to 155?mg?kg?1 in roots of C. praecox. Dominant As compounds were arsenite and arsenate with a small abundance of dimethylarsinic acid (DMA) in all the plant species. In Cyperaceae, small percentages of arsenobetaine (AB) and arsenocholine (AC) were detected, suggesting the ability of these plants to transform As into less toxic compounds. Moreover, the important role of As(V) sequestration on iron plaque on the root surface of Cyperaceae was confirmed. In this context, root washing with oxalic acid partially disrupted the iron plaque for the better release of arsenate.  相似文献   

20.
Soils from two typical tidal salt marshes with varied salinity in the Yellow River Delta wetland were analysed to determine possible effects of salinity on soil carbon sequestration through changes in soil microbiology. The mean soil respiration (SR) of the salt water–fresh water mixing zone (MZ) was 2.89 times higher than that of the coastal zone (CZ) (4.73 and 1.63?μmol?m?2?s?1, respectively, p?Pseudomonas sp. and Limnobacter sp. that might have led to its higher dehydrogenase activity and respiratory rates. Additionally, the CZ possessed more Halobacteria and Thaumarchaeota with the ability to fix CO2 than the MZ. Significantly lower soil salinity in MZ (4.25?g?kg?1) was suitable for β-Proteobacteria, but detrimental for Halobacteria compared with CZ (7.09?g?kg?1, p?相似文献   

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