Xylene isomers, including -xylene (X), -xylene (X), -xylene (X), and ethyl benzene (EB), are important raw materials in industry. The separation of xylene isomers has been recognized as one of the "seven chemical separations to change the world". However, because of their similar physicochemical properties, totally separating four xylene isomers has remained a big challenge until now. Metal-organic frameworks (MOFs) have emerged as promising separators to achieve this goal because MOFs synergistically provide multiple mechanisms at the molecular scale. In this review, we summarize the recent progress of MOFs as separators for the separation of xylenes based on four main separation mechanisms: the molecular sieving effect, gating mechanism, thermodynamic interactions, and kinetic diffusion. We concentrate on the applications of MOFs in the field of chromatography, single-component vapor adsorption, liquid-phase competitive adsorption, breakthrough, and membrane separation. Finally, we conclude with the possible direction for designing high-performance MOF separators and briefly discuss the existing challenges in this area.
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Angew Chem Int Ed Engl
January 2025
Tsinghua University, Institute of Nuclear and New Energy Technology, Room A320, Nengke Building, Qinghua Yuan No.1, Beijing, CHINA.
Exploring host-guest interactions to regulate hydrogen-bonding assembly offers a promising approach for developing advanced porous crystal materials (PCMs). However, screening compatible guests with appropriate geometries and host-guest interactions that could inhibit the dense packing of building blocks remains a primary challenge. This study presents a novel guest-induced crystallization (GIC) strategy, guided by thermodynamic calculations, to develop porous hydrogen-bonded organic frameworks (HOFs) using structurally challenging tetrazole building units.
View Article and Find Full Text PDFChem Soc Rev
January 2025
Jiangsu Key Laboratory of Biofunctional Materials, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, Jiangsu Key Laboratory of New Power Batteries, College of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.
J Environ Manage
December 2024
School of Environmental Sciences, University of Guelph, 50 Stone Rd E, Guelph, ON, N1H 2W1, Canada. Electronic address:
Hybrid poplars are widely recognized for their effectiveness in remediating subsurface aromatic hydrocarbon contaminants, including benzene, toluene, ethylbenzene, and xylene isomers (BTEX). While BTEX compounds are frequently found in the transpiration streams of poplars at contaminated sites, the microbial dynamics within these trees, particularly in response to hydrocarbon exposure, remain underexplored. This study utilized high-throughput amplicon sequencing to investigate the trunk microbiome in hybrid poplars at a field-scale toluene phytoremediation site.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Nankai University, Colege of Chemistry, CHINA.
Organic photovoltaic materials that can be processed via non-halogenated solvents are crucial for the large-area manufacturing of organic solar cells (OSCs). However, the limited available of electron acceptors with adequate solubility and favorable molecular packing presents a challenge in achieving efficient non-halogenated solvent-processed OSCs. Herein, inspired by the three-dimensional dimeric acceptor CH8-4, we employed a molecular isomerization strategy to synthesize its isomers, CH8-4A and CH8-4B, by tuning the position of fluorine (F) atom in the central unit.
View Article and Find Full Text PDFEnviron Sci Process Impacts
December 2024
Department of Chemistry, University of Toronto, Canada.
Proton transfer reaction mass spectrometry (PTR-MS) is often employed to characterize gas-phase compounds in both indoor and outdoor environments. PTR-MS measurements are usually made without upstream chromatographic separation, so it can be challenging to differentiate between an ion of interest, its isomers, and fragmentation products from other species all detected at the same mass-to-charge ratio. These isomeric contributions and fragmentation interferences can confound the determination of accurate compound mixing ratios, the assignment of accurate chemical properties, and corresponding analyses of chemical fate.
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