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Separation of enantiomers is an everlasting challenge in chemistry, catalysis, and synthesis of pharmaceuticals. The design and fabrication of chiral adsorbent materials is a promising way to increase the surface area of chiral information, as well as to maximize the available surface for the adsorption of one enantiomer. Porous materials such as silica or metal-organic-frameworks are established compounds in this field, due to their well-defined surface structure and ease of functionalization with chiral groups. As another class of porous materials, carbons provide the advantages of high thermal and chemical stability, resistance against moisture, electrical conductivity, and widely tunable pore size. Although they are well established in many adsorption-related applications, carbons received far less attention in enantioselective adsorption processes because the controlled functionalization of their surface is rather difficult due to the chemically heterogeneous atoms in the network. A suitable approach to overcome this limitation is the synthesis of chiral carbons directly from chiral precursors. So far, chiral carbons synthesized from chiral precursors used salt-templating as a way of introducing porosity, which resulted in mainly microporous materials or materials with broad pore size distribution. In the present study, the possibility of combining nanocasting as an alternative templating approach with chiral ionic liquids as a carbon precursor is demonstrated. Chiral recognition is measured in the gas phase, by adsorption of chiral gas, as well as in the solution, by using isothermal titration calorimetry. (C) 2020 Elsevier Ltd. All rights reserved.
In this study, a phosphorus recovery product, struvite palygorskite (S-PAL), obtained from nutrient-rich wastewater by using MgO modified palygorskite was applied for copper remediation in aqueous solution and contaminated soil to achieve waste recycling. The effects of contact time, initial pH, initial Cu(II) concentration and reaction temperature on Cu(II) adsorption in aqueous solution were intensively testified. Pseudo-second-order model was able to properly describe Cu(II) adsorption kinetics by using palygorskite (PAL) and S-PAL, and S-PAL exhibited higher adsorption amount (106.27 mg/g) than PAL (8.46 mg/g) at pH of 4. Cu(II) adsorption on PAL and S-PAL could be well fitted by Freundlich isotherm and Langmuir isotherm, respectively. The calculated thermodynamic parameters indicated that Cu(II) adsorption onto PAL and S-PAL were spontaneous and endothermic. A 28-day soil incubation experiment was conducted to evaluate the effects of PAL and S-PAL with three different rates (1%, 5% and 10% w/w) on Cu immobilization in contaminated soil. In the immobilization test, Cu extracted by 0.01 mol/L CaCl2 after seven days incubation significantly decreased with increasing rate of PAL and S-PAL. BCR sequential extraction results showed the significant decrease of acid soluble Cu and a concomitant increase of the residual fraction of Cu after S-PAL and PAL addition. XRD patterns of soil samples after treatment by PAL and S-PAL showed the formation of Cu0.6Mg1.3Si2O6 and Cu-3.04(PO4)(2)OH0.08 center dot 2H(2)O, which indicated that silanol groups and phosphate exhibited affinity for Cu in the soil.