Sorption selectivity of birnessite particle edges: a d-PDF analysis of Cd(ii) and Pb(ii) sorption by δ-MnO2 and ferrihydrite

2016 ◽  
Vol 18 (8) ◽  
pp. 1030-1041 ◽  
Author(s):  
Case M. van Genuchten ◽  
Jasquelin Peña

Birnessite minerals (layer-type MnO2), which bear both internal (cation vacancies) and external (particle edges) metal sorption sites, are important sinks of contaminants in soils and sediments.

2005 ◽  
Vol 277-279 ◽  
pp. 438-444 ◽  
Author(s):  
Sung Eun Lee ◽  
Jin Soo Lee ◽  
Hyo Taek Chon

In order to investigate the extent and degree of heavy metal contamination in soils and sediments influenced by past mining activities, and to estimate the effects of indigenous bacteria on Cd speciation and bioremoval efficiency in sediments according to the various environmental conditions, tailings, soils, waters and sediments were collected from the Hwacheon Au-Ag-Pb-Zn mine in Korea. Elevated levels of metals, i.e., 29 As mg/kg, 30 Cd mg/kg, 261 Cu mg/kg, 601 Pb mg/kg and 3128 Zn mg/kg were found in sediments. High concentrations of As and other heavy metals in soils, waters and sediments were found near the tailings piles. From the results of sequential extraction analyses with tailings and soils, a high proportion of Cd is present as non-residual fractions. This indicates that Cd is more mobile and bioavailable than Cu, Pb and Zn. For seasonal variation, the concentrations of As and other heavy metals were much more elevated in soils collected before rainy season than after rainy season. To estimate the bioremoval efficiency for Cd, bacteria which can adsorb Cd were isolated from sediments in this area. Microorganisms in sediments can alter the mobility of heavy metals and bacteria can leach heavy metals from sediments, adsorb them on their cell wall and accumulate them within an intracellular matrix. From the metal sorption tests with indigenous bacteria, the bioremoval efficiency of Cd in Cd single solution (10 ppm) was more than 90%. As well, the isolated bacterial strains exhibited a preferential metal sorption , i.e., Cd > Pb > Zn for single metal solutions and Pb > Cd > Zn for the mixed metal solutions. Therefore, the use of some microorganisms to remove heavy metals from contaminated sediments may represent an innovative purification process.


2006 ◽  
Vol 14 (2) ◽  
pp. 340-344
Author(s):  
A. Seech ◽  
D. Raymond ◽  
J. Moreno
Keyword(s):  

2020 ◽  
Author(s):  
Amy Lam ◽  
◽  
Todd Longbottom ◽  
Nelli K. Bodiford ◽  
Omar R. Harvey

2021 ◽  
Vol 3 (3) ◽  
Author(s):  
Péter Sipos

AbstractStudies comparing numerous sorption curve models and different error functions are lacking completely for soil-metal adsorption systems. We aimed to fill this gap by studying several isotherm models and error functions on soil-metal systems with different sorption curve types. The combination of fifteen sorption curve models and seven error functions were studied for Cd, Cu, Pb, and Zn in competitive systems in four soils with different geochemical properties. Statistical calculations were carried out to compare the results of the minimizing procedures and the fit of the sorption curve models. Although different sorption models and error functions may provide some variation in fitting the models to the experimental data, these differences are mostly not significant statistically. Several sorption models showed very good performances (Brouers-Sotolongo, Sips, Hill, Langmuir-Freundlich) for varying sorption curve types in the studied soil-metal systems, and further models can be suggested for certain sorption curve types. The ERRSQ error function exhibited the lowest error distribution between the experimental data and predicted sorption curves for almost each studied cases. Consequently, their combined use could be suggested for the study of metal sorption in the studied soils. Besides testing more than one sorption isotherm model and error function combination, evaluating the shape of the sorption curve and excluding non-adsorption processes could be advised for reliable data evaluation in soil-metal sorption system.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Aastha Vasdev ◽  
Moinak Dutta ◽  
Shivam Mishra ◽  
Veerpal Kaur ◽  
Harleen Kaur ◽  
...  

AbstractA remarkable decrease in the lattice thermal conductivity and enhancement of thermoelectric figure of merit were recently observed in rock-salt cubic SnTe, when doped with germanium (Ge). Primarily, based on theoretical analysis, the decrease in lattice thermal conductivity was attributed to local ferroelectric fluctuations induced softening of the optical phonons which may strongly scatter the heat carrying acoustic phonons. Although the previous structural analysis indicated that the local ferroelectric transition temperature would be near room temperature in $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te , a direct evidence of local ferroelectricity remained elusive. Here we report a direct evidence of local nanoscale ferroelectric domains and their switching in $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te using piezoeresponse force microscopy(PFM) and switching spectroscopy over a range of temperatures near the room temperature. From temperature dependent (250–300 K) synchrotron X-ray pair distribution function (PDF) analysis, we show the presence of local off-centering distortion of Ge along the rhombohedral direction in global cubic $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te . The length scale of the $${\text {Ge}}^{2+}$$ Ge 2 + off-centering is 0.25–0.10 Å near the room temperatures (250–300 K). This local emphatic behaviour of cation is the cause for the observed local ferroelectric instability, thereby low lattice thermal conductivity in $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te .


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Katharina R. Lenhardt ◽  
Hergen Breitzke ◽  
Gerd Buntkowsky ◽  
Erik Reimhult ◽  
Max Willinger ◽  
...  

AbstractWe report here on structure-related aggregation effects of short-range ordered aluminosilicates (SROAS) that have to be considered in the development of synthesis protocols and may be relevant for the properties of SROAS in the environment. We synthesized SROAS of variable composition by neutralizing aqueous aluminium chloride with sodium orthosilicate at ambient temperature and pressure. We determined elemental composition, visualized morphology by microscopic techniques, and resolved mineral structure by solid-state 29Si and 27Al nuclear magnetic resonance and Fourier-transform infrared spectroscopy. Nitrogen sorption revealed substantial surface loss of Al-rich SROAS that resembled proto-imogolite formed in soils and sediments due to aggregation upon freezing. The effect was less pronounced in Si-rich SROAS, indicating a structure-dependent effect on spatial arrangement of mass at the submicron scale. Cryomilling efficiently fractured aggregates but did not change the magnitude of specific surface area. Since accessibility of surface functional groups is a prerequisite for sequestration of substances, elucidating physical and chemical processes of aggregation as a function of composition and crystallinity may improve our understanding of the reactivity of SROAS in the environment.


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