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https://www.selleckchem.com/products/otx015.html For the first time, the existence of a unique dispersivity of a double-porosity medium at a given saturation was demonstrated for different transport scenarios of initial and boundary conditions. The saturation dependence of the dispersivity in the double-porosity medium was established and compared with the trends obtained for the single-porosity soils in previous studies.Engineered black carbon (biochar) can be introduced into groundwater through its extensive engineered applications (e.g., in-situ remediation of groundwater/soils), which can participate in geochemical processes that may alter the fate of trace contaminants such as arsenic (As(III)). Here we examined the impacts of the undissolved and dissolved fractions of reduced biochar (hereafter denoted as rUBC and rDBC, respectively) on the As(III) immobilization in the absence/presence of Ca2+ (50 mM) at pH 11.5 under anoxic conditions. While neither rUBC nor rDBC alone was capable of immobilizing As(III), the apparent As(III) immobilization by rUBC and rDBC synergistically occurred in the presence of Ca2+, with an efficiency of 73.1% and 89.6% within 24 h, respectively. In the rUBC/Ca2+/As(III) system, rUBC enabled full oxidation of As(III) to As(V) by its residual redox-active moieties such as quinoid CO and persistent free radicals, thereby facilitating precipitation of the newly generated As(V) with Ca2+ adsorbed onto the rUBC's surface. In contrast, rDBC induced in-situ local enrichment of Ca2+ in the nascent rDBC-derived flocs with predominant non-oxidative and slight oxidative precipitation of As(III) via ternary rDBC-Ca-As complexation. This ternary complex was created by Ca2+-bridging interactions between As species and oxygen-containing functional groups of rDBC, as evidenced by the FTIR results and the Ca2+-impeded As(III) oxidation. The generation of the flocs physically trapped a small amount of As species particularly As(III). Both the increases

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