6 research outputs found

    The Surge of Metal–Organic-Framework (MOFs)-Based Electrodes as Key Elements in Electrochemically Driven Processes for the Environment

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    Metal–organic-frameworks (MOFs) are emerging materials used in the environmental electrochemistry community for Faradaic and non-Faradaic water remediation technologies. It has been concluded that MOF-based materials show improvement in performance compared to traditional (non-)faradaic materials. In particular, this review outlines MOF synthesis and their application in the fields of electron- and photoelectron-Fenton degradation reactions, photoelectrocatalytic degradations, and capacitive deionization physical separations. This work overviews the main electrode materials used for the different environmental remediation processes, discusses the main performance enhancements achieved via the utilization of MOFs compared to traditional materials, and provides perspective and insights for the further development of the utilization of MOF-derived materials in electrified water treatment

    Hierarchically Porous Carbon Materials for CO<sub>2</sub> Capture: The Role of Pore Structure

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    With advances in porous carbon synthesis techniques, hierarchically porous carbon (HPC) materials are being utilized as relatively new sorbents for CO<sub>2</sub> capture applications. These HPC materials were used as a platform to prepare samples with differing textural properties and morphologies to elucidate structure–property relationships. It was found that high microporous content, rather than overall surface area, was of primary importance for predicting good CO<sub>2</sub> capture performance. Two HPC materials were analyzed, each with near identical high surface area (∼2700 m<sup>2</sup>/g) and colossally high pore volume (∼10 cm<sup>3</sup>/g), but with different microporous content and pore size distributions, which led to dramatically different CO<sub>2</sub> capture performance. Overall, large pore volumes obtained from distinct mesopores were found to significantly impact adsorption performance. From these results, an optimized HPC material was synthesized that achieved a high CO<sub>2</sub> capacity of ∼3.7 mmol/g at 25 °C and 1 bar

    Dynamic Adsorption of CO<sub>2</sub>/N<sub>2</sub> on Cation-Exchanged Chabazite SSZ-13: A Breakthrough Analysis

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    Alkali-exchanged SSZ-13 adsorbents were investigated for their applicability in separating N<sub>2</sub> from CO<sub>2</sub> in flue gas streams using a dynamic breakthrough method. In contrast to IAST calculations based on equilibrium isotherms, K<sup>+</sup> exchanged SSZ-13 was found to yield the best N<sub>2</sub> productivity, comparable to Ni-MOF-74, under dynamic conditions where diffusion properties play a significant role. This was attributed to the selective, partial blockage of access to the chabazite cavities, enhancing the separation potential in a 15/85 CO<sub>2</sub>/N<sub>2</sub> binary gas mixture

    An Efficient, Solvent-Free Process for Synthesizing Anhydrous MgCl<sub>2</sub>

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    A new efficient and solvent-free method for the synthesis of anhydrous MgCl<sub>2</sub> from its hexahydrate is presented. Fluidized dehydration of MgCl<sub>2</sub>·6H<sub>2</sub>O feedstock at 200 °C in a porous bed reactor yields MgCl<sub>2</sub>·nH<sub>2</sub>O (0 < n < 1), which has a similar diffraction pattern as activated MgCl<sub>2</sub>. The MgCl<sub>2</sub>·nH<sub>2</sub>O is then ammoniated directly using liquefied NH<sub>3</sub> in the absence of solvent to form MgCl<sub>2</sub>·6NH<sub>3</sub>. Calcination of the hexammoniate complex at 300 °C then yields anhydrous MgCl<sub>2</sub>. Both dehydration and deammoniation were thoroughly studied using <i>in situ</i> as well as <i>ex situ</i> characterization techniques. Specifically, a detailed understanding of the dehydration process was monitored by <i>in situ</i> PXRD and <i>in situ</i> FTIR techniques where formation of salt with nH<sub>2</sub>O (n = 4, 2, 1, <1) was characterized. Given the reduction in thermal energy required to produce dehydrated feedstock with this method compared with current strategies, significant cost benefits are expected. Overall, the combined effect of activation, macroporosity, and coordinated water depletion allows the formation of hexammoniate without using solvent, thus minimizing waste formation
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