Kinetic research on the sorption of aqueous cadmium on carbonate hydroxyapatite     

Yu LIU Huanyan XU 《中国地球化学学报》2006,25(B08):104-105

The sorption of aqueous cadmium on carbonate-hydroxyapatite （CHap） is a complicated non-homogeneous solid/water reaction, From kinetic point of view, it can be described by two stages： at the earlier stage, reaction rate is so fast that its kinetic course is intricate, and at the later stage, the rate of reaction becomes slow and the process of reaction accords with one order reaction kinetic equation. Experimental results show that the relationship between reaction rate constant kl and temperature T accords to Arrhenius Equation, and the activation energy of sorption （Ea） is 6.075 J/mol and frequency factor （A） is 220 s^-1. At the same time, reaction rate constant kl increases with decreasing Cd^2＋ initial concentration, on the contrary, with increasing pH and CHap dosage.  相似文献   

高岭石和硅／铝-氧化物对腐殖酸的吸附实验研究   总被引：10，自引：6，他引：10       下载免费PDF全文

吴宏海张秋云  方建章曾丽璇 《岩石矿物学杂志》2003,22(2):173-176

矿物结合的腐殖质可改变矿物的表面性质,矿物对腐殖酸的吸附强度与矿物的吸附位性质、密度、荷电性及比表面积有关.若按比表面积计算,矿物对腐殖酸的吸附强度顺序为氢氧化铝>高岭石>石英;按单位质量计算,吸附强度顺序为高岭石>氢氧化铝>石英.研究表明,矿物表面活性受水溶液pH值的调控,且当pH值在4～7时,上述3种矿物对腐殖酸的吸附机理为石英主要表现为氢键作用;氢氧化铝主要表现为配体交换表面配位作用;高岭石表现为多种形式并存,包括氢键、配体交换表面配位和疏水性作用以及金属离子桥键作用.  相似文献   

Numerical simulation of transport and sequential biodegradation of chlorinated aliphatic hydrocarbons using CHAIN_2D     

J. Schaerlaekens  D. Mallants  J. S&#x;imûnek  M. Th. Van Genuchten  J. Feyen 《水文研究》1999,13(17):2847-2859

Microbiological degradation of perchloroethylene (PCE) under anaerobic conditions follows a series of chain reactions, in which, sequentially, trichloroethylene (TCE), cis‐dichloroethylene (c‐DCE), vinylchloride (VC) and ethene are generated. First‐order degradation rate constants, partitioning coefficients and mass exchange rates for PCE, TCE, c‐DCE and VC were compiled from the literature. The parameters were used in a case study of pump‐and‐treat remediation of a PCE‐contaminated site near Tilburg, The Netherlands. Transport, non‐equilibrium sorption and biodegradation chain processes at the site were simulated using the CHAIN_2D code without further calibration. The modelled PCE compared reasonably well with observed PCE concentrations in the pumped water. We also performed a scenario analysis by applying several increased reductive dechlorination rates, reflecting different degradation conditions (e.g. addition of yeast extract and citrate). The scenario analysis predicted considerably higher concentrations of the degradation products as a result of enhanced reductive dechlorination of PCE. The predicted levels of the very toxic compound VC were now an order of magnitude above the maximum permissible concentration levels. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

Contaminant transport with non‐equilibrium processes in unsaturated soils and implicit characteristic Galerkin scheme     

Xikui Li  Wenhua Wu  S. Cescotto 《国际地质力学数值与分析法杂志》2000,24(3):219-243

A non‐equilibrium sorption—advection—diffusion model to simulate miscible pollutant transport in saturated–unsaturated soils is presented. The governing phenomena modelled in the present simulation are: convection, molecular diffusion, mechanical dispersion, sorption, immobile water effect and degradation, including both physical and chemical non‐equilibrium processes. A finite element procedure, based on the characteristic Galerkin method with an implicit algorithm is developed to numerically solve the model equations. The implicit algorithm is formulated by means of a combination of both the precise and the traditional numerical integration procedures. The stability analysis of the algorithm shows that the unconditional stability of the present implicit algorithm is enhanced as compared with that of the traditional implicit numerical integration procedure. The numerical results illustrate good performance of the present algorithm in stability and accuracy, and in simulating the effects of all the mentioned phenomena governing the contaminant transport and the concentration distribution. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   

Human resource management and competitive advantage: An application of resource-based view in the shipping industry     

Maria Progoulaki  Ioannis Theotokas 《Marine Policy》2010

The resource-based view (RBV) of the firm has been established as one of the main approaches to strategy formulation for the development of sustainable competitive advantage. Moreover, human resource management can be conceptualised as a source of competitiveness. This paper proposes that RBV could contribute to the confrontation of the hindrances that shipping companies face in the management of their human resources, and to the formation of sustainable competitive advantage. The paper analyses the findings of a field study, regarding the different human resource and crew management practices that are applied by Greek-owned shipping companies. Finally, based on the RBV of the firm, it proposes an integrated framework for managing human resources in the shipping industry in a way that could lead to the formation of sustainable competitive advantage.  相似文献   

Suspended Particles: Their Role in Estuarine Biogeochemical Cycles   总被引：11，自引：0，他引：11  

A. Turner  G. E. Millward 《Estuarine, Coastal and Shelf Science》2002,55(6):857

Suspended particles are instrumental in controlling the reactivity, transport and biological impacts of substances in aquatic environments, and provide a crucial link for chemical constituents between the water column, bed sediment and food chain. This article reviews the role of suspended particles in the chemical and biological cycling of trace constituents (trace metals, organo-metallic compounds and hydrophobic organic micropollutants; HOMs) in estuaries, with particular emphasis on the effects of and changes to particle reactivity and composition.The partitioning (or distribution coefficient,K_D ) and bioavailability of chemical constituents, and assimilation efficiency (AE) of such by bivalve suspension feeders, are identified as key parameters requiring definition for accurate biogeochemical modelling, and the discussion centres around the determination of and controls on these parameters. Particle-water interactions encompass a variety of physical, biological, electrostatic and hydrophobic effects, and are largely dependent on the character and concentration of suspended particles and salinity. The salinity-dependence results from the competing and complexing effects of seawater ions for trace metals, and the compression of water in the presence of dissolved seawater ions and consequent salting out of neutral solute (HOMs, organo-metallic compounds and some trace metal complexes). The extent of biological solubilization of chemical constituents from suspended particles is dependent on the nature of chemical components of the gastro-intestinal environment and their interactions with ingested particles, and the physiological (e.g. gut passage time) and chemical (e.g. redox conditions and pH) constraints imposed on these interactions. Generally, chemicals that associate with fine, organic-rich particles (or, for some HOMs, fine inorganic particles), and desorb at pH 5–6 and/or complex with digestive enzymes or surfactants are most readily solubilized in the gut. The extent of assimilation of solubilized chemical is then determined by its ability to pass the gut lining and partition into cytosolic material.In practice, K_D and AE are determined experimentally by means of radiotracers added to contained suspensions or mesocosms, while operational measurement of bioavailability relies on in vitro chemical or biological (enzymatic) extraction of particles. What is lacking, however, and is identified as an ultimate goal of future research, is the ability to predict these parameters from theoretical principles and thermodynamic constants. Since many of the inherent interactions and mechanisms are controlled by particle composition and reactivity, a more immediate objective would be better characterization of the biogeochemical properties of suspended particles themselves. This includes chemical resolution of the bulk organic matter, definition of the abundance and synergistic effects of component sorbent phases, and determination of the effects of particle-seawater ion interactions on the reactivity of the particle surface.  相似文献   

Competitive adsorption,release and speciation of heavy metals in the Yellow River sediments,China   总被引：2，自引：0，他引：2  

Qingyun Fan  Jiang He  Hongxi Xue  Changwei LÜ  Ying Liang  Saruli  Ying Sun  Lili Shen 《Environmental Geology》2007,53(2):239-251

The competitive adsorption and the release of selected heavy metals and their speciation distribution before and after adsorption in the Yellow River sediments are discussed. The adsorption of metals onto sediments increases with increasing pH value and decreases with increasing ionic strength. The competitive coefficient K _c and the distribution coefficient K _d are obtained to analyze the competitive abilities of selected heavy metals, which are ranked as Pb > Cu >> Zn > Cd. The competition among selected heavy metals becomes more impetuous with increasing ion concentration in water. Speciation analysis was done by an improved analytical procedure involving five steps of sequential extraction. Cu, Pb and Zn were mainly transformed into the carbonate-bound form (50.8–87.7%) in adsorption. Most of (60.7–77.3%) Cd was transformed into the exchangeable form, and the percentage of carbonate-bound Cd was 19.7–30.4%. The release reaction was so quick that the release capacity of selected heavy metals from sediments to aqueous solution reached half of the maximum value only in 30 s. As opposed to adsorption, the release capacities of selected heavy metals were ranked as Cd > Zn >> Cu > Pb. In this study, Cd produces the most severe environmental hazards, because its concentration in the release solution is 85.8 times more than the human health criteria of US EPA.  相似文献   

Modeling the effects of nonlinear equilibrium sorption on the transport of solute plumes in saturated heterogeneous porous media     

A. Abulaban  J. L. Nieber 《Advances in water resources》2000,23(8)

Transport of sorbing solutes in 2D steady and heterogeneous flow fields is modeled using a particle tracking random walk technique. The solute is injected as an instantaneous pulse over a finite area. Cases of linear and Freundlich sorption isotherms are considered. Local pore velocity and mechanical dispersion are used to describe the solute transport mechanisms at the local scale. This paper addresses the impact of the degree of heterogeneity and correlation lengths of the log-hydraulic conductivity field as well as negative correlation between the log-hydraulic conductivity field and the log-sorption affinity field on the behavior of the plume of a sorbing chemical. Behavior of the plume is quantified in terms of longitudinal spatial moments: center-of-mass displacement, variance, 95% range, and skewness. The range appears to be a better measure of the spread in the plumes with Freundlich sorption because of plume asymmetry. It has been found that the range varied linearly with the travelled distance, regardless of the sorption isotherm. This linear relationship is important for extrapolation of results to predict behavior beyond simulated times and distances. It was observed that the flow domain heterogeneity slightly enhanced the spreading of nonlinearly sorbing solutes in comparison to that which occurred for the homogeneous flow domain, whereas the spreading enhancement in the case of linear sorption was much more pronounced. In the case of Freundlich sorption, this enhancement led to further deceleration of the solute plume movement as a result of increased retardation coefficients produced by smaller concentrations. It was also observed that, except for plumes with linear sorption, correlation between the hydraulic conductivity and the sorption affinity fields had minimal effect on the spatial moments of solute plumes with nonlinear sorption.  相似文献   

Sorption of ortho‐Phenylphenol to Soils     

Chunli Zheng  Andreas Focks  Katrin Ellebrake  Till Eggers  Elke Fries 《洁净——土壤、空气、水》2011,39(2):116-120

Conflicting sorption coefficients for ortho‐phenylphenol (OPP) have been reported in the literatures, which resulted in the conflicting assessments on OPP mobility in soil. To ascertain the sorption coefficient of OPP, batch experiments were performed based on OECD guideline 106, using three types of soils. Headspace solid‐phase microextraction (HS‐SPME) and GC‐MS were applied to the determination of OPP concentration in the liquid phase. The sorption isotherms obtained for all three soils under equilibrium conditions were described well, assuming linear sorption. The organic carbon normalized distribution coefficients (K_oc) ranged from 894 to 1703 L kg^?1, which suggested that OPP is moderately mobile in soil. The results also showed that the K_oc value of OPP can be predicted precisely from K_ow, whereas it was underestimated by one order of magnitude when water solubility is used.  相似文献   

模拟土样有机碳和矿物质对TCE吸附贡献的实验研究   总被引：2，自引：0，他引：2  

韩璐  何江涛  张晶  张坤峰 《岩石矿物学杂志》2011,30(6):1118-1124

为研究均一介质条件下有机碳含量及矿物质对TCE吸附行为的影响,简化了土壤环境的复杂性和异质性,以固定矿物质(高岭土∶石英砂=3∶7)作为土壤基体,添加不同质量分数的腐殖质(foc=0.16%~2.29%)配制成模拟土样,进行矿物质和模拟土样对TCE的吸附批实验。实验结果显示,TCE的吸附等温线呈非线性。随有机碳含量增加,表现为线性吸附增强,矿物质对TCE的吸附贡献随有机碳含量增加而减小。foc>0.82%时,矿物质对吸附作用的贡献率<5%;foc>1%时,可以基本忽略矿物质对吸附的影响。此外,TCE初始浓度也会影响有机碳和矿物质的吸附能力。用Freundlich模型分别拟合TCE吸附等温线的低浓度段和高浓度段(以Ce=500μg/L为浓度高低的分界),Freundlich指数n值呈现由大到小的趋势;TCE初始浓度越高,有机碳的吸附贡献率相对上升,而矿物质的贡献率则下降。TCE初始浓度在50~500μg/L之间、foc由0.16%增大到1%时,矿物质的吸附贡献率范围由28%~16%缩小到3%~1%之间,此时TCE初始浓度对有机碳和矿物质的吸附贡献率基本没有影响。  相似文献