6 research outputs found
The Surge of Metal–Organic-Framework (MOFs)-Based Electrodes as Key Elements in Electrochemically Driven Processes for the Environment
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
Molecular Insight into Fluorocarbon Adsorption in Pore Expanded Metal–Organic Framework Analogs
International audienc
Hierarchically Porous Carbon Materials for CO<sub>2</sub> Capture: The Role of Pore Structure
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
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>
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