Effective separation of ethyne from ethyne/ethylene (C H /C H ) mixtures is a challenging and crucial industrial process. Herein, an ultra-microporous metal-organic framework (MOF) platform, Cd(dicarboxylate) (ditriazole), with triangular channels is proposed for high-efficiency separation of C H from C H . The targeted structures are constructed via a mixed-ligand strategy by selecting different-sized ligands, allowing for tunable pore sizes and volumes. The pore properties can be further optimized by additional modification via pore environment tailoring. This concept leads to the successful synthesis of three ultra-microporous Cd-MOFs (JLU-MOF87-89). As intended, C H uptake and C H /C H selectivity gradually increase with progressively optimizing the pore structure by adjusting ligand length and substituents. JLU-MOF89, functionalized with methyl groups, features the most optimal pore chemistry and shows selective recognition of C H over C H , owing to the framework-C H host-guest interactions. Furthermore, JLU-MOFs are fabricated into mixed-matrix membranes for C H /C H separation. C H permeability and C H /C H permselectivity are substantially enhanced by ≥400% and ≥200%, respectively, after hybridization of JLU-MOF88 and JLU-MOF89 with a polyimide polymer (6FDA-ODA). These membranes can work efficiently and are stable under different conditions, demonstrating their potential in actual ethyne separation.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/adma.202204553 | DOI Listing |
Small
November 2024
Institut des Matériaux Poreux de Paris, Ecole Normale Supérieure, ESPCI Paris, CNRS, PSL University, Paris, 75005, France.
Nitric oxide (NO), a key element in the regulation of essential biological mechanisms, presents huge potential as therapeutic agent in the treatment and prevention of chronic diseases. Metal-organic frameworks (MOFs) with open metal sites are promising carriers for NO therapies but delivering it over an extended period in biological media remains a great challenge due to i) a fast degradation of the material in body fluids and/or ii) a rapid replacement of NO by water molecules onto the Lewis acid sites. Here, a new ultra-narrow pores Fe bisphosphonate MOF, denoted MIP-210(Fe) or Fe(HO)(Hmbpa) (Hmbpa = p-xylenediphosphonic acid) is described that adsorbs NO due to an unprecedented sorption mechanism: coordination of NO through the Fe(III) sites is unusually preferred, replacing bound water, and creating a stable interaction with the free HO and P-OH groups delimiting the ultra-narrow pores.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2024
College of Chemical Engineering and Technology, Shanxi Key Laboratory of Gas Energy Efficient and Clean Utilization, Taiyuan University of Technology, Taiyuan 030024, Shanxi, PR China. Electronic address:
For ethylene purification, CH-selective metal-organic frameworks (MOFs) show great potential to directly produce polymer-grade CH from CH/CH mixtures. Most CH-traping MOFs are ultra-microporous structures so as to strengthen multiple supramolecular interactions with CH. However, the narrowed pore channels of CH-traping MOFs cause large guest diffusion barriers, greatly hampering their practical applications.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
April 2024
Institut des Matériaux Poreux de Paris, ESPCI Paris, Ecole Normale Supérieure, CNRS, PSL University, 75005, Paris, France.
The improvement of the Total Isomerization Process (TIP) for the production of high-quality gasoline with the ultimate goal of reaching a Research Octane Number (RON) higher than 92 requires the use of specific sorbents to separate pentane and hexane isomers into classes of linear, mono- and di-branched isomers. Herein we report the design of a new multi-cage microporous Fe(III)-MOF (referred to as MIP-214, MIP stands for materials of the Institute of Porous Materials of Paris) with a flu-e topology, incorporating an asymmetric heterofunctional ditopic ligand, 4-pyrazolecarboxylic acid, that exhibits an appropriate microporous structure for a thermodynamic-controlled separation of hydrocarbon isomers. This MOF produced via a direct, scalable, and mild synthesis route was proven to encompass a unique separation of C5/C6 isomers by classes of low RON over high RON alkanes with a sorption hierarchy: (n-hexane≫n-pentane≈2-methylpentane>3-methylpentane)≫(2,3-dimethylbutane≈i-pentane≈2,2-dimethylbutane) following the adsorption enthalpy sequence.
View Article and Find Full Text PDFMolecules
August 2023
CNPC Petrochemical Research Institute Company Limited, Beijing 102206, China.
Developing metal-organic framework (MOF) adsorbents with excellent performance and robust stability is of critical importance to reduce CO emissions yet challenging. Herein, a robust ultra-microporous MOF, Cu(bpfb)(bdc), with mixed ligands of N, N'-(1,4-phenylene)diisonicotinamide (bpfb), and 1,4-dicarboxybenzene (bdc) was delicately constructed. Structurally, this material possesses double-interpenetrated frameworks formed by two staggered, independent frameworks, resulting in two types of narrow ultra-micropores of 3.
View Article and Find Full Text PDFCommun Chem
July 2023
Institut des Matériaux Poreux de Paris, Ecole Normale Supérieure, ESPCI Paris, CNRS, PSL University, 75005, Paris, France.
Al-based cationic metal-organic frameworks (MOFs) are uncommon. Here, we report a cationic Al-MOF, MIP-213(Al) ([Al(μ-OH)(OH)(mdip)]6Cl·6HO) constructed from flexible tetra-carboxylate ligand (5,5'-Methylenediisophthalic acid; Hmdip). Its crystal structure was determined by the combination of three-dimensional electron diffraction (3DED) and high-resolution powder X-ray diffraction.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!