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1.
《Applied Geochemistry》1993,8(3):273-283
A new model for base cation release due to chemical weathering of soil minerals has been developed based on transition state theory, and included in the integrated soil chemistry model PROFILE. The data required for model application can be operationally determined on soil samples, making the model generally applicable and independent of any type of calibration. The model considers the contribution to the weathering rate from 12 groups of the most common primary and secondary minerals of soils, reacting in separate reactions with H+-ion, H2O, CO2 and organic acids expressed as dissolved organic carbon (DOC). The weathering rate sub-model couples the effects of dissolved Al and base cations on the reaction mechanisms. The model takes into account changes in soil temperature, different chemical conditions, the effect of vegetation interactions with the soil and N transformations. The kinetic coefficients and reaction orders are based on a complete re-evaluation of weathering data available in the literature, and additional kinetic data determined by the authors.Data from 23 different independent determinations of the field weathering rate from 15 sites in Scandinavia, Central Europe and North America were compiled and used to verify the model. The model is capable of estimating the release rate of base cations due to chemical weathering from information on soil mineralogy, texture and geochemical properties of the order of ±20% of the rate determined by independent methods. The results indicate that small amounts of dark minerals like epidote and hornblende, and the plagioclase content, largely determine the field weathering rate.  相似文献   

2.
The adsorbent properties of dried water hyacinth root biomass towards four polar solvents (dichloromethane, ethyl acetate, diethyl ether and acetone) were studied by inverse gas chromatography between 40 and 70 °C. The enthalpy of adsorption values obtained for the adsorption of the four solvents on untreated root biomass range from ?51.234 kJ mol?1 for acetone, an amphoteric solvent, to ?74.658 kJ mol?1 for dichloromethane, an acidic solvent. Mineral acid and organic solvent treatment led to reduction in the values of the enthalpy of adsorption for all four solvents. The Lewis acidity parameters calculated from the enthalpy of adsorption values were 0.408, 0.267 and 0.356, while the corresponding Lewis basicity parameters were 3.76, 1.80 and 2.34, respectively, for untreated, mineral acid-treated and organic solvent-treated water hyacinth root biomass. The Lewis basicity parameter-to-Lewis acidity parameter ratios for the untreated, acid-treated and organic solvent-treated biomass were found to be 9.22, 6.74 and 6.57, respectively, indicating (a) that all the surfaces of the untreated, mineral acid-treated and organic solvent-treated water hyacinth root biomass are basic in nature and (b) that for all volatile polar solvents studied, the adsorption interaction involves the lowest unoccupied molecular orbital of the solvent as the electron acceptor and the highest occupied molecular orbital of the water hyacinth root biomass surface adsorbent site as the electron donor.  相似文献   

3.

The site characterization of unsaturated soils is well stablished based on laboratory tests, which are expensive and time-consuming. In-situ testing methods, such as the flat dilatometer test (DMT), are an alternative to the traditional approach of drilling, sampling, and laboratory testing. The literature on DMT interpretation is well established on saturated and well-behaved soils. Only few studies deal with DMT interpretation in unusual soils, and little is known about the influence of soil suction on this test. This paper presents and discusses the influence of soil suction on four DMT campaigns carried out in an unsaturated tropical soil site, also incorporating the soil suction influence on the DMT interpretation. Soil suction was estimated by the soil–water characteristic curve (SWCC) and water content profiles. The water content profiles range from 11.3 to 19.7% which corresponds to a suction range estimated by SWCCs mostly between 6 and 200 kPa. Soil suction significantly influenced DMT data up to 5 m depth at the studied site (the unsaturated active zone) increasing the intermediate DMT parameters. The average horizontal stress index (KD) was equal to about 1.7 and the average dilatometer modulus (ED) was about 4.7 MPa in the active zone and practically doubled their values due to in situ soil suction. The estimated peak friction angle (?) was 20–30% higher due to soil suction influence on DMT assuming the soil behaves as a sand like material. Soil suction must be considered to assess the behavior of the investigated soil by the DMT. The suction influence should be incorporated in the effective stress and this approach considerably improved the site characterization of the studied site.

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4.
对松花江一级阶地包气带的岩性特征分析结果表明,三层介质均为砂土,有机质和粘土矿物含量较少,水的渗透系数由袁层到深层显著增大.阿特拉津在三层介质中的吸附系数依次为1.2 mL/g、0.6 mL/g和0.2 mL/g,自然降解半衰期为124 d、153 d和225 d,能够长期残留在包气带中,构成对地下水的威胁.  相似文献   

5.
Mobility of organic solvents in water-saturated soil materials   总被引：1，自引：0，他引：1  
This investigation presents an analysis of the mobility of 37 organic solvents in saturated soil-water systems, focusing on adsorption phenomena at the solid-liquid interface This analysis was made, in part, by applying predictive expressions that estimate the potential magnitude of adsorption by soil materials Of the 37 solvents considered, 19 were classified as either “very highly mobile” or “highly mobile” and, thus, would have little tendency to be retained by soils to a significant extent, 12 were considered to have medium mobility and 6 low mobility None of these solvents were in the immobile class The limited information available indicates that these predictive expressions yield satisfactory first approximations of the magnitude of adsorption of these solvents by soil materials  相似文献   

6.
To understand Phosphorus (P) sources and transport processes in the subsurface in Bwaise III Parish, Kampala, P attenuation and adsorption capacities of soils were studied in situ and from laboratory measurements. Relationships between sorption parameters and soil matrix properties, rates and mechanism of the adsorption process and soil P fractions were also investigated. P was generally higher in the wet than the dry season, but for both seasons, the maximum was 5 mgP/l. P transport mechanisms appeared to be a combination of adsorption, precipitation, leaching from the soil media and by colloids with the latter two playing an important role in the wet season. The sorption process comprised two phases with the first stage rate constants being about fourfold those of the second stage. The Langmuir isotherm described the sorption data well (R 2 ≥ 0.95) with the second soil layer exhibiting the highest sorption maximum (C max) (average value 0.6 ± 0.17 mgP/gDW). The best prediction of C max had organic carbon, Ca, available P and soil pH. Residual P consisting mostly of organics was the main fraction in all the layers followed by inorganic HCl-P and NaOH-P in the top and middle layers, respectively. Loosely bound P (NH4Cl-P) was the least fraction (<0.4% of total P) in all layers indicating the high binding capacity of P by the soils. The study results suggest that P dynamics is related to Ca, Fe and organic carbon content of the soils.  相似文献   

7.
Eleven Chinese immature source rock concentrates from the immature oil formations in four different depressions were extracted ultrasonically with a mixture of CS2 and N-methyl-2-pyrrolidinone (CS2/NMP) at room temperature. The samples were also extracted with CHCl3 and a mixture of methanol/acetone/chloroform (MAC) for comparison. The solvent system CS2/NMP is very efficient for the extraction of immature source rock concentrates, giving much higher extraction yields than CHCl3 or MAC. The composition of the extracts using different solvent mixtures is also different. Model compound tests indicate that no chemical reactions have taken place between the NMP and the substrates in the extraction. These results suggest that there are abundant non-covalent bond interactions in the organic matter of the immature source rock concentrates. The fact that CS2/NMP mixed solvent extracts more than MAC and CHCl3 is not only because it can dissolve higher molecular weight fractions, but also because it has stronger ability to disrupt the complex interactions existing between the soluble and insoluble fractions. Biomarker distributions in the saturated hydrocarbon fractions are different for different solvent systems, suggesting that care should be taken when comparing the biomarker parameters in source rocks when using different solvents for extraction.  相似文献   

8.
《Applied Geochemistry》2006,21(1):166-183
The composition of organic matter (OM) in pine vegetation and soil samples from a pine forest which was charred by a wildfire was analyzed using solid-state nuclear magnetic resonance (13C NMR) and gas chromatography–mass spectrometry (GC–MS) of solvent extracts to study the effects of thermal alteration on soil organic matter (SOM). The NMR data revealed the presence of unaltered biomolecules (cellulose, proteins) and low contents of aromatic C (15%) in the charred pine wood and cones while the charred soil samples exhibited higher contents of aromatic C (39–56%). The solvent extraction of charred and uncharred plant and soil samples yielded diterpenoids, triterpenoids, steroids, a series of aliphatic lipids, phenols and carbohydrates indicating the predominant input of higher plant OM and minor contributions from microorganisms and/or fauna. The lower yield of solvent extractable aliphatic lipids in the charred samples versus the uncharred samples suggests that these compounds are thermally degraded during a wildfire. Molecular markers for the burning of cellulose (levoglucosan, mannosan, galactosan) were detected in all charred samples. The comparison of charred and uncharred samples allowed the identification of unaltered pine derived biomolecules and their thermal alteration products in the charred samples. Terpenoid and steroid biomolecules were in part altered during incomplete combustion to aromatic, unsaturated and polar derivatives (“pyromolecules”) that still retained the characteristic skeleton of their precursors. Since some of the polar degradation products found in the charred soils can be generated either from thermal or microbial degradation, the aromatic and unsaturated hydrocarbon products are preferred as molecular markers for SOM burning. Ratios of biological precursors to aromatic (diterpenoids) or unsaturated products (steroids) indicate that the cyclic lipids in the pine wood and the soil surface horizon were highly altered. In conclusion, the solvent extractable lipids and carbohydrates in charred SOM are valuable, source-specific molecular markers for the burning of plant biomass and for tracing the biogeochemistry of charred residues in soils.  相似文献   

9.
Zou  Haifeng  Zhang  Nan  Puppala  Anand J. 《Acta Geotechnica》2019,14(6):2007-2029

Soil thermal conductivity (k) is a key parameter for the design of energy geo-structures, and it depends on many soil properties such as saturation degree, porosity, mineralogical composition, soil type and others. Capturing these diversified influencing factors in a soil thermal conductivity model is a challenging task for engineers due to the nonlinear dependencies. In this study, a multivariate distribution approach was utilized to improve an existing soil thermal conductivity model, Cote and Konrad model, by quantitatively considering the impacts of dry density (ρd), porosity (n), saturation degree (Sr), quartz content (mq), sand content (ms) and clay content (mc) on thermal conductivity of unsaturated soils. A large database containing these seven soil parameters was compiled from the literature to support the multivariate analysis. Simplified bivariate and multivariate correlations for improving the Cote and Konrad model were derived analytically and numerically to consider different influencing factors. By incorporating these simplified correlations, the predicted k values were more concentrated around the measured values with the coefficient of determination (R2) increased from 0.83 to 0.95. It is concluded that the developed correlations with the information of different soil properties provide an efficient, rational and simple way to predict soil thermal conductivity more accurately. Moreover, the quartz content is a more important factor than the porosity that shall be considered in the establishment of thermal conductivity models for unsaturated soils with high quartz content.

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10.
Available data on silicate/liquid, phosphate/liquid and oxide/liquid trace element partition coefficients from experimental studies show an encouraging degree of consistency, although much more work is required before a set of coefficients of wide-ranging application to planetary problems can be compiled. The complex dependences of most coefficients on bulk chemical composition (and liquid structure) are important aspects which remain to be fully resolved. Further determinations of coefficients for a number of elements for phosphates, zircon, spinels, amphiboles and garnets are especially desirable and investigations into the effects of pressure and volatiles on the magnitudes of partition coefficients are also needed. There is a major discrepancy among existing data regarding the upper concentration limits of Henry's Law dilute solution behavior under different experimental conditions. Data obtained at 1 atmosphere under dry conditions can apparently be reconciled with data from highpressure, H2O-saturated experiments only if Henry's Law limits are themselves functions of variables such as pressure, temperature, H2O activity and chemical composition. Further experiments (including studies bearing on the role of defect substitution at very low trace element concentrations) are required to resolve this question.  相似文献   

11.
Batch experiments were performed to investigate cephapirin (a widely used veterinary antibiotic) adsorption on various size sands of low total organic carbon content (0.08–0.36 wt%). In the aqueous concentration range investigated (11–112 μmol/L cephapirin), adsorption to nearly pure quartz filter sands (0.50–3.35 mm diameter) is low. Isotherms are S-shaped and most display a region of minimum adsorption, where decreased adsorption occurs with increasing solution concentration, followed by increased adsorption at higher concentrations. Cephapirin adsorption to quartz-rich, feldspar-bearing dune sands (0.06–0.35 mm diameter), and the smallest quartz filter sand investigated (0.43–0.50 mm), can be described by linear sorption isotherms over the range of concentrations investigated. Distribution coefficients (K d) range from 0.94 to 3.45 L/kg. No systematic relationship exists between grain size and amount of adsorption for any of the sands investigated. Cephapirin adsorption is positively correlated to the feldspar ratio (K-feldspar/(albite + Ca-plagioclase). Feldspar-ratio normalization of distribution coefficients was more effective than organic carbon normalization at reducing variability of K d values in the dune sands investigated.  相似文献   

12.
This study aimed to evaluate boron (B) adsorption and the capacity of a surface complexation model for simulating this process in calcareous soils. Ten surface soils were collected from different land use areas in Hamedan, Western Iran, to characterize B sorption by soils. The mean B adsorbed by the sample soils varied from 8.9 to 32.8 %. Two empirical models including linear and Freundlich equations fitted well to the experimental data. The linear distribution (K d) values varied from 1.32 to 6.86 L kg?1, while the parameters of Freundlich equation including n and K Fr ranged from 1.16 to 1.33 and 3.31–16.81, respectively. The comparison of two empirical models indicated that B adsorption followed a nonlinear pattern. The soil organic matter had positive correlations with Freundlich and linear distribution coefficients. However, empirical models were not suitable for explaining the mechanism of B adsorption, so a surface complexation model was used to simulate and predict the B adsorption process. B adsorption modeling was conducted using Visual MINTEQ and PHREEQC, based on the assemblage of major surface components (hydrous ferric oxides, aluminum hydroxides, calcium carbonate, and humic acids). B adsorption was successfully modeled by surface complexation. The significant contribution of organic matter to B complexes was resulted from both experimental data and mechanistic modeling.  相似文献   

13.
Simultaneous competitive adsorption behavior of Cd, Cu, Pb and Zn onto nine soils with a wide physical–chemical characteristics from Eastern China was measured in batch experiments to assess the mobility and retention of these metals in soils. In the competitive adsorption system, adsorption isotherms for these metals on the soils exhibited significant differences in shape and in the amount adsorbed. As the applied concentration increased, Cu and Pb adsorption increased, while Cd and Zn adsorption decreased. Competition among heavy metals is very strong in acid soils with lower capacity to adsorb metal cations. Distribution coefficients (K dmedium) for each metal and soil were calculated. The highest K dmedium value was found for Pb and followed by Cu. However, low K dmedium values were shown for Zn and Cd. On the basis of the K dmedium values, the selectivity sequence of the metal adsorption is Pb > Cu > Zn > Cd and Pb > Cu > Cd > Zn. The adsorption sequence of nine soils was deduced from the joint distribution coefficients (K dΣmedium). This indicated that acid soils with low pH value had lower adsorption capacity for heavy metals, resulting in much higher risk of heavy metal pollution. The sum of adsorbed heavy metals on the soils could well described using the Langmuir equation. The maximum adsorption capacity (Q m) of soils ranged from 32.57 to 90.09 mmol kg−1. Highly significant positive correlations were found between the K dΣmedium and Q m of the metals and pH value and cation exchange capacity (CEC) of soil, suggesting that soil pH and CEC were key factors controlling the solubility and mobility of the metals in soils.  相似文献   

14.
Carbon dioxide and nitrogenous gases in the soil atmosphere   总被引：1，自引：0，他引：1  
Carbon dioxide and nitrogenous trace gases (N2O, NO) in the soil atmosphere are mainly the products of microbially mediated processes. Once produced, these gases pass to the overlying atmosphere primarily via molecular diffusion, a process which is described by Fick's law of diffusion.In a diffusion-dominated soil, the partial pressure, or concentration, of CO2 in the soil atmosphere varies as a function of soil depth and is dependent on the production rate and diffusivities. Since these parameters are highly variable, CO2 concentrations vary widely both between, and within, differing ecosystems. In a compilation of data from around the world, arranged according to an ecosystem classification, soil CO2 concentrations varied from 0.04 to 13.0% by volume in the upper several meters of soil. These data also highlight the importance of organic substrate (soil organic matter, roots, root exudates), temperature, and (to some extent) moisture on CO2 production and the resulting concentration in soil profiles. The δ13C of the soil CO2 also varies as a function of depth due to differences in the δ13C of the organic substrate undergoing decomposition and the mixing with CO2 of the overlying atmosphere. Recent work suggests that the δ18O of the soil CO2 may hold some promise in estimating the δ18O of soil water.Biological production and consumption of N2O and NO results primarily from activity of nitrifying and denitrifying bacteria. Ammonium limitation of nitrification and organic carbon limitation of denitrification usually restricts these processes to surface soil horizons, although denitrification may be an important process for reducing NO3− in groundwater. These microbial processes and the relative proportions of their gaseous end products are strongly influenced by redox conditions. Microsite variation in sources of electron donors and acceptors is critical to understanding rates and distributions of N trace gas production. Several abiological oxidation and reduction reactions are also important, and interaction of biological and abiological processes deserves more research attention.  相似文献   

15.
Mechanistic roles of soil humus and soil minerals and their contributions to soil sorption of nonionic organic compounds from aqueous and organic solutions are illustrated. Parathion and lindane are used as model solutes on two soils that differ greatly in their humic and mineral contents. In aqueous systems, observed sorptive characteristics suggest that solute partitioning into the soil-humic phase is the primary mechanism of soil uptake. By contrast, data obtained from organic solutions on dehydrated soil partitioning into humic phase and adsorption by soil minerals is influenced by the soil-moisture content and by the solvent medium from which the solute is sorbed.  相似文献   

16.
An analytical solution to 1D coupled water infiltration and deformation in layered soils is derived using a Laplace transformation. Coupling between seepage and deformation, and initial conditions defined by arbitrary continuous pore‐water pressure distributions are considered. The analytical solutions describe the transient pore‐water pressure distributions during 1D, vertical infiltration toward the water table through two‐layer unsaturated soils. The nonlinear coupled formulations are first linearized and transformed into a form that is solvable using a Laplace transformation. The solutions provide a reliable means of comparing the accuracy of various numerical methods. Parameters considered in the coupled analysis include the saturated permeability (ks), desaturation coefficient (α), and saturated volumetric water content (θs) of each soil layer, and antecedent and subsequent rainfall infiltration rates. The analytical solution demonstrates that the coupling of seepage and deformation plays an important role in water infiltration in layered unsaturated soils. A smaller value of α or a smaller absolute value of the elastic modulus of the soil with respect to a change in soil suction (H) for layered unsaturated soils means more marked coupling effect. A smaller absolute value of H of the upper layer soil also tends to cause more marked coupling effect. A large difference between the saturated coefficients of permeability for the top and bottom soil layers leads to reduced rainfall infiltration into the deep soil layer. The initial conditions also play a significant role in the pore‐water pressure redistribution and coupling effect. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

17.
The removal of caffeine from tap water by F-400 granular activated carbon in fixed-bed adsorption experiments was carried out. Textural and chemical characterization of the adsorbent through N2 adsorption–desorption isotherms, Fourier transform infrared spectrometry, isoelectric point determination and scanning electron microscopy studies was developed in studies previously reported. Caffeine breakthrough curves and total organic carbon profiles at different operation conditions (inlet concentration, volumetric flow rate and mass of adsorbent) were obtained. These experimental results showed a displacement of the natural organic matter from the active sites exerted by caffeine molecules due to their higher affinity to the surface carbon. This behavior led to an overshooting, a local outlet natural organic matter concentration higher than the feed quantity. A competitive effect seems to be observed in the removal of the target compound, decreasing the efficiency of the process. Axial dispersion coefficients and dimensionless numbers were estimated for the caffeine removal onto F-400 activated carbon. Therefore, the regeneration of the adsorbent by adsorption–desorption cycles was studied.  相似文献   

18.
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19.
对中国南方的3个水稻土样品进行了Cd、Pb单一离子和混合离子吸附特点的研究。结果表明,3个水稻土样品中Cd、Pb的吸附特点都相似,Langmuir等温方程可很好地描述Cd、Pb的吸附等温线。3个土壤样品中,有较高pH值和较低有机物、CEC浓度、粘土含量、高岭石含量的2个土壤样品对Cd、Pb有较大的吸附量,且其等温吸附拟合的最大吸附量（B）也较大。在两组分混合溶液中,尽管共存离子的存在影响了土壤对单一离子的吸附,同时土壤对Cd的吸附在一定程度上受影响的程度大,但3个土壤样品都表现出对Pb有强的吸附能力。在3个土壤样品中,Langmuir等温方程中Pb的健合能常数（K）都大于Cd的健合能常数（K）,混合溶液中的K值高于单一溶液的K值,表明2种金属离子对吸附位点的竞争提高了特定吸附位点的保持力,使金属离子在土壤中特定位点的吸附更加坚固。  相似文献   

20.
对中国南方的3个水稻土样品进行了Cd、Pb单一离子和混合离子吸附特点的研究。结果表明,3个水稻土样品中Cd、Pb的吸附特点都相似,Langmuir等温方程可很好地描述Cd、Pb的吸附等温线。3个土壤样品中,有较高pH值和较低有机物、CEC浓度、粘土含量、高岭石含量的2个土壤样品对Cd、Pb有较大的吸附量,且其等温吸附拟合的最大吸附量(B)也较大。在两组分混合溶液中,尽管共存离子的存在影响了土壤对单一离子的吸附,同时土壤对Cd的吸附在一定程度上受影响的程度大,但3个土壤样品都表现出对Pb有强的吸附能力。在3个土壤样品中,Langmuir等温方程中Pb的健合能常数(K)都大于Cd的健合能常数(K),混合溶液中的K值高于单一溶液的K值,表明2种金属离子对吸附位点的竞争提高了特定吸附位点的保持力,使金属离子在土壤中特定位点的吸附更加坚固。  相似文献   

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