High Cu and Cd pollution in sediments from Sisimiut, Greenland. Adsorption to organic matter and fine particles

High concentrations of Cu of up to 200 mg/kg, and Cd of up to 4.0 mg/kg, were found in sediments from the aquatic environment around Sisimiut, Greenland. These concentrations are four times higher than the limiting concentration where toxicological effects are expected. The pollution could be linked to human activities in Sisimiut, a link that have not been investigated previously in Greenland. Except from the most polluted samples there was good correlation between heavy metal concentration and organic matter. Also some relationship between fine fraction and heavy metal concentration was observed.     

普通小球藻和铜绿微囊藻与粘土颗粒凝聚沉降行为研究

本研究结果表明,不同的藻类和不同的粘土颗粒均使藻类与粘土颗粒的凝聚沉降发生变化。结果还表明,溶液中[Cu~(2+)]浓度超过10~(-5)mol后,加快了小球藻与高龄土的凝聚沉降。使80％以上的小球藻和高岭土在不到10min内即凝聚沉降。在最后结合实验结果讨论了利用藻类与粘土的凝聚沉降治理水体污染。     

Non-aqueous-phase-liquid breakthrough during evaporative drying of clay barriers

In this study, an attempt has been made to model a real field scenario, whereby an initially almost saturated clay liner in a waste site is gradually drying, due to evaporation at its lower boundary. A detailed conceptual model that deals with the penetration and breakthrough of non-aqueous-phase-liquid (NAPL) in clay liners is introduced. Water content of clay samples was monitored during ambient evaporation through apertures at the base of sample holders. Clay drying rate served as the primary parameter for the NAPL breakthrough study. The interconnection between drying rates, structural damage formation (cracks and suction) and NAPL penetration is especially addressed. The processes taking place in the clay samples during drying appear to be associated with the capillary effects between the different fluid phases in the vicinity of either the NAPL-clay or the clay-air boundaries. A conceptual model of NAPL penetration and breakthrough of the clay layer has been considered, based on both indirect and direct observations of structural damages produced on either clay boundaries. A mutual interaction between these two boundaries is suggested and discussed. NAPL breakthrough is suggested to take place through cracks initiated on the upper soil surface.     

Explicit and implicit coupling during solute transport through clay membrane barriers

Simulations of salt (KCl) flux through a 1-m-thick clay membrane barrier (CMB) based on coupled solute transport theory are compared to simulated fluxes based on traditional advective-dispersive transport theory. The simulations are based on measured values for the effective salt-diffusion coefficient (Ds*) and chemico-osmotic efficiency coefficient (omega) for a bentonite-based barrier material subjected to KCl solutions. The results indicate that the exit salt flux is reduced due to both explicit coupling (hyperfiltration and chemico-osmotic counter-advection) and an implicit coupling effect resulting from the decrease in Ds* due to a decrease in the apparent tortuosity factor, tau a, with an increase in omega. Implicit coupling is shown to be more significant than explicit coupling for reducing and retarding salt flux through a CMB under diffusion-dominated conditions. Failure to account for the implicit coupling effect may result in unrealistic results, such as the existence of salt flux through a perfect (ideal) clay membrane (i.e., omega=1).     

均质化莲子草根系分泌物对黏土吸附四环素的影响

在不同比例空心莲子草粗根(TR)和细根(FR)分泌物均质化条件下,研究膨润土和高岭土对四环素(TC)的等温吸附特征,并分析pH值、温度和离子浓度对TC吸附的影响.结果表明,分泌物均质化后黏土对TC的吸附符合Henry模型,FR均质化对TC吸附的促进作用比TR均质化更强,高岭土对TC吸附的增长幅度比膨润土更大;在pH值2...     

Fluorosis caused by indoor coal combustion in China: discovery and progress

In this study, investigations into endemic fluorosis were conducted and fluorine concentration in environmental samples determined. In an indoor coal-combustion-type fluorosis area, local clay was used to mix with coal for indoor combustion. There are two key steps in the procedure of the indoor transition of fluorine: indoor wet corns and vegetables strongly absorbed fluorine from indoor air; and fluorine strongly accumulated in clay, which was mixed with coal for combustion. Therefore, with the increasing of the percentage of clay in the clay-mixed coal as well as corn in foodstuff, the ratio of fluorosis will be increased.     

Sorption of tylosin on clay minerals

The equilibrium sorption of tylosin (TYL) on kaolinite and montmorillonite was measured at different solution pH using batch reactor systems. The results showed that all the sorption isotherms were nonlinear and that the nonlinearity decreased as the solution pH increased for a given clay. At a specific aqueous concentration, the single-point sorption distribution coefficient (K_D) of TYL decreased rapidly as the solution pH increased. A speciation-dependent sorption model that accounted for the contributions of the cationic and neutral forms of TYL fit the data well, suggesting that the sorption may be dominated by both ion exchange and hydrophobic interactions. The isotherm data also fit well to a dual mode model that quantifies the contributions of a site-limiting Langmuir component (ion exchange) and a non-specific linear partitioning component (hydrophobic interactions). X-ray diffraction analyses revealed that the interlayers of montmorillonite were expanded due to the uptake of TYL. TYL molecules likely form a monolayer surface coverage.     

膨润土粘土矿吸附焦化废水中氨氮的研究

研究了膨润土粘土矿对碳酸铵溶液中ＮＨ４＾＋离子和焦化废水中氨氮的吸附。结果表明：在低液固比时，颗粒膨润土对碳酸铵溶液中ＮＨ４＾＋离子的吸附效果优于粉状膨润土；在高液固化时，粉状膨润土的吸附效果优于颗粒膨润土。颗粒膨润土对焦化废水中氨氮的吸附效果优于粉状膨润土和活化膨润土。     

Modelling of silica diffusion experiments with Si in Boom Clay

A mathematical model describing the dissolution of nuclear glass directly disposed in clay combines a first-order dissolution rate law with the diffusion of dissolved silica in clay. According to this model, the main parameters describing the long-term dissolution of the glass are ηR, the product of the diffusion accessible porosity η and the retardation factor R, and the apparent diffusion coefficient D_app of dissolved silica in clay.For determining the migration parameters needed for long-term predictions, four Through-Diffusion (T-D) experiments and one percolation test have been performed on undisturbed clay cores. In the Through-Diffusion experiments, the concentration decrease after injection of ³²Si (radioactive labelled silica) was measured in the inlet compartment. At the end of the T-D experiments, the clay cores were cut in thin slices and the activity of labelled silica in each slice was determined. The measured activity profiles for these four clay cores are well reproducible.Since no labelled silica could be detected in the outlet compartments, the Through-Diffusion experiments are fitted by two In-Diffusion models: one model assuming linear and reversible sorption equilibrium and a second model taking into account sorption kinetics. Although the kinetic model provides better fits, due to the sufficiently long duration of the experiments, both models give approximately similar values for the fit parameters. The single percolation test leads to an apparent diffusion coefficient value about two to three times lower than those of the Through-Diffusion tests.Therefore, dissolved silica appears to be strongly retarded in Boom Clay. A retardation factor R between 100 and 300 was determined. The corresponding in situ distribution coefficient K_d is in the range 25–75 cm³ g⁻¹. The apparent diffusion coefficient of dissolved silica in Boom Clay is estimated between 2×10⁻¹³ and 7×10⁻¹³ m² s⁻¹. The pore diffusion coefficient is in the range from 6×10⁻¹¹ to 1×10⁻¹⁰ m² s⁻¹.     

Simultaneous sorption of lead and chlorobenzene by organobentonite

Clays or organoclays have been used as a barrier to prevent the transport of hazardous contaminants in landfills. However, clays are known to effectively sorb mostly inorganic contaminants, while organoclays are mainly used for organic contaminants. Since the organoclays are basically clay particles modified with cationic surfactants, there might exist an optimal coverage of cationic surfactant on the clay particles to sorb both inorganic and organic contaminants. In order to determine the optimal mass of cationic surfactants on the bentonites, sodium bentonites were treated with various ratios of hexadecyltrimethylammonium (HDTMA) to bentonites. Chlorobenzene and lead were selected as representative contaminants. When either chlorobenzene or lead exists as a single contaminant, chlorobenzene sorption increased with increasing HDTMA to bentonite ratios, and lead sorption decreased with increasing HDTMA to bentonite ratios. Sorption of chlorobenzene was a function of HDTMA coverage on the bentonites, while lead sorption was much more influenced by the initial lead concentration rather than the mass of HDTMA added to the bentonites.