Architecting Ultra-Robust Zr(IV) Metal-Organic Framework for Energy-Efficient Desiccant Air Conditioning.

Air-conditioning systems, composed mainly of humidity control and heat reallocation units, play a pivotal role in upholding superior air quality and human well-being across diverse environments ranging from international space stations and pharmacies to granaries and cultural relic preservation sites, and to commercial and residential buildings. The adoption of sorbent water as the working pair and low-grade renewable or waste heat in adsorption-driven air-conditioning presents a state-of-the-art solution, notably for its energy efficiency and eco-friendliness vis-à-vis conventional electricity-driven vapor compression cycles. Here, we introduce a rational π-extension strategy to engineer an ultrarobust and highly porous zirconium metal-organic framework (Zr-MOF).

Separation of High-Purity CH from Binary CH/CO Using Robust Al-Based MOFs Comprising Nitrogen-Containing Heterocyclic Dicarboxylate.

In this study, three nitrogen-containing aluminum-based metal-organic frameworks (Al-MOFs), namely, CAU-10pydc, MOF-303, and KMF-1, were investigated for the efficient separation of a CH/CO gas mixture. Among these three Al-MOFs, KMF-1 demonstrated the highest selectivity for CH/CO separation (6.31), primarily owing to its superior CH uptake (7.

Design of Pore Properties of an Al-Based Metal-Organic Framework for the Separation of an Ethane/Ethylene Gas Mixture via Ethane-Selective Adsorption.

A series of Al-based isomorphs (CAU-10H, MIL-160, KMF-1, and CAU-10pydc) were synthesized using isophthalic acid (ipa), 2,5-furandicarboxylic acid (fdc), 2,5-pyrrole dicarboxylic acid (pyrdc), and 3,5-pyridinedicarboxylic acid (pydc), respectively. These isomorphs were systematically investigated to identify the best adsorbent for effectively separating CH/CH. All CAU-10 isomorphs exhibited preferential adsorption of CH over that of CH in mixture.

Tuning Hydrophilicity of Aluminum MOFs by a Mixed-Linker Strategy for Enhanced Performance in Water Adsorption-Driven Heat Allocation Application.

Water adsorption-driven heat transfer (AHT) technology has emerged as a promising solution to address crisis of the global energy consumption and environmental pollution of current heating and cooling processes. Hydrophilicity of water adsorbents plays a decisive role in these applications. This work reports an easy, green, and inexpensive approach to tuning the hydrophilicity of metal-organic frameworks (MOFs) by incorporating mixed linkers, isophthalic acid (IPA), and 3,5-pyridinedicarboxylic acid (PYDC), with various ratios in a series of Al-xIPA-(100-x)PYDC (x: feeding ratio of IPA) MOFs.

An Amine-Functionalized Ultramicroporous Metal-Organic Framework for Postcombustion CO Capture.

Among the most promising methods by which to capture CO from flue gas, the emission of which has accelerated global warming, is energy-efficient physisorption using metal-organic framework (MOF) adsorbents. Here, we present a novel cuprous-based ultramicroporous MOF, (adci = 2-amino-4,5-dicyanoimidazolate), which was rationally synthesized by combining two strategies to design MOF physisorbents for enhanced CO capturing, i.e.

High-Performance Adsorbent for Ethane/Ethylene Separation Selected through the Computational Screening of Aluminum-Based Metal-Organic Frameworks.

The development of a high-performance ethane (CH)-selective adsorbent for the separation of ethane/ethylene (CH/CH) gas mixtures has been investigated for high-efficiency adsorption-based gas separation. Herein, we investigated Al-based metal-organic frameworks (MOFs) to identify an efficient CH-selective adsorbent (CAU-11), supported by a computational simulation study. CAU-11 exhibited numerous advantageous properties (such as low material cost, structural robustness, high reaction yield, and high CH/CH selectivity) compared to other Al-based MOFs, indicating immense potential as a CH-selective adsorbent.

Separation of Branched Alkanes Feeds by a Synergistic Action of Zeolite and Metal-Organic Framework.

Zeolites and metal-organic frameworks (MOFs) are considered as "competitors" for new separation processes. The production of high-quality gasoline is currently achieved through the total isomerization process that separates pentane and hexane isomers while not reaching the ultimate goal of a research octane number (RON) higher than 92. This work demonstrates how a synergistic action of the zeolite 5A and the MIL-160(Al) MOF leads to a novel adsorptive process for octane upgrading of gasoline through an efficient separation of isomers.

Crystals springing into action: metal-organic framework CUK-1 as a pressure-driven molecular spring.

Mercury porosimetry and high pressure single crystal X-ray diffraction revealed the wine-rack CUK-1 MOF as a unique crystalline material capable of a fully reversible mechanical pressure-triggered structural contraction. The near-absence of hysteresis upon cycling exhibited by this robust MOF, akin to an ideal molecular spring, is associated with a constant work energy storage capacity of 40 J g. Molecular simulations were further deployed to uncover the free-energy landscape behind this unprecedented pressure-responsive phenomenon in the area of compliant hybrid porous materials.

Catalytic Performance of Zr-Based Metal-Organic Frameworks Zr-abtc and MIP-200 in Selective Oxidations with H O.

The catalytic performance of Zr-abtc and MIP-200 metal-organic frameworks consisting of 8-connected Zr clusters and tetratopic linkers was investigated in H O -based selective oxidations and compared with that of 12-coordinated UiO-66 and UiO-67. Zr-abtc demonstrated advantages in both substrate conversion and product selectivity for epoxidation of electron-deficient C=C bonds in α,β-unsaturated ketones. The significant predominance of 1,2-epoxide in carvone epoxidation, coupled with high sulfone selectivity in thioether oxidation, points to a nucleophilic oxidation mechanism over Zr-abtc.

Water adsorption fingerprinting of structural defects/capping functions in Zr-fumarate MOFs: a hybrid computational-experimental approach.

Engineering structural defects in MOFs has been intensively applied to modulate their adsorption-related properties. Zr-fumarate MOF (also known as MOF-801) is a prototypical defective MOF with proven versatile adsorption/separation performances depending on the synthetic conditions, however the relationship between the nature/concentration of both structure defects/capping functions and its adsorption features is still far from being fully understood. In this work, we first present a systematic theoretical exploration of the individual contributions of linker and cluster defects as well as of the capping functions to the overall water adsorption profile of the MOF-801 framework.

Defective Zr-Fumarate MOFs Enable High-Efficiency Adsorption Heat Allocations.

Adsorption-driven heat transfer devices incorporating an efficient "adsorbent-water" working pair are attracting great attention as a green and sustainable technology to address the huge global energy demands for cooling and heating. Herein, we report the improved heat transfer performance of a defective Zr fumarate metal-organic framework (MOF) prepared in a water solvent ( HT). This material exhibits an S-shaped water sorption isotherm (/ = 0.

Rational design of a robust aluminum metal-organic framework for multi-purpose water-sorption-driven heat allocations.

Adsorption-driven heat transfer technology using water as working fluid is a promising eco-friendly strategy to address the exponential increase of global energy demands for cooling and heating purposes. Here we present the water sorption properties of a porous aluminum carboxylate metal-organic framework, [Al(OH)(CHNO)]·nHO, KMF-1, discovered by a joint computational predictive and experimental approaches, which exhibits step-like sorption isotherms, record volumetric working capacity (0.36 mL mL) and specific energy capacity (263 kWh m) under cooling working conditions, very high coefficient of performances of 0.

Unique design of superior metal-organic framework for removal of toxic chemicals in humid environment via direct functionalization of the metal nodes.

Unique chemical and thermal stabilities of a zirconium-based metal-organic framework (MOF) and its functionalized analogues play a key role to efficiently remove chemical warfare agents (ex., cyanogen chloride, CNCl) and simulant (dimethyl methylphosphonate, DMMP) as well as industrial toxic gas, ammonia (NH). Herein, we for the first time demonstrate outstanding performance of MOF-808 for removal of toxic chemicals in humid environment via special design of functionalization of hydroxo species bridging Zr-nodes using a triethylenediamine (TEDA) to form ionic frameworks by gas phase acid-base reactions.

Porous Metal-Organic Framework CUK-1 for Adsorption Heat Allocation toward Green Applications of Natural Refrigerant Water.

The development of new water adsorbents that are hydrothermally stable and can operate more efficiently than existing materials is essential for the advancement of water adsorption-driven chillers. Most of the existing benchmark materials and related systems in this field suffer from clear limitations that must be overcome to meet global requirements for sustainable and green energy production and utilization. Here, we report the energy-efficient water sorption properties of three isostructural metal-organic frameworks (MOFs) based on the simple ligand pyridine-2,4-dicarboxylate, named M-CUK-1 [M(μ-OH)(2,4-pdc)] (where M = Co, Ni, or Mg).

Molecular Encapsulation of Trimeric Chromium Carboxylate Clusters in Metal-Organic Frameworks and Propylene Sorption.

Oxo-bridged trimeric chromium acetate clusters [Cr O(OOCCH ) (H O) ]NO have been encapsulated for the first time in the mesoporous cages of the chromium terephthalate MIL-101(Cr). The isolated clusters in MIL-101(Cr) have increased affinity towards propylene compared to propane, due to generation of a new kind of pocket-based propylene-binding site, as supported by DFT calculations.

Spring-Based Active Shock Absorber Systems with Piezoelectric Energy Harvesters.

In this research, energy harvesters with different types of spring-based shock absorbers were invested for the active shock absorber applications. Two different types of spring-based shock absorbers were prepared for the comparison, coil type spring-based shock absorbers and specially designed slice type spring-based shock absorbers. Shock absorbers have been widely employed to protect the complicated main system by cancelling the applied mechanical forces from outsides.

Flexible Energy Harvester Based on Poly(vinylidene fluoride) Composite Films.

In these days, we are facing emerging energy crisis due to depletion of fossil fuels. Therefore, renewable energy which is based on wind energy, mechanical force energy, microwave energy and vibrations energy have attracted a lot of attentions. Piezoelectric energy harvesting is one of the promising renewable energy sources.

Enhanced Ferroelectric and Piezoelectric Properties of (1-)PMN-PT Ceramics Based on a Partial Oxalate Process.

The pyrochlore phase in ferroelectric and piezoelectric materials is the main obstacle device application due to its poor electrical properties. Especially, the pyrochlore phase is frequently observed in the perovskite-based metal-oxide materials including piezoelectric and ferroelectric ceramics, which are based on solid-state reaction methods for fabrication. To overcome these problems, advanced innovative methods such as partial oxalate process will be investigated.

Piezoelectric Energy Generators Based on Spring and Inertial Mass.

In this study, inertial mass-based piezoelectric energy generators with and without a spring were designed and tested. This energy harvesting system is based on the shock absorber, which is widely used to protect humans or products from mechanical shock. Mechanical shock energies, which were applied to the energy absorber, were converted into electrical energies.

Can pelagic ciliates indicate vertical variation in the water quality status of western Arctic pelagic ecosystems?

The vertical pattern of pelagic ciliate communities was observed at eight layers in the Chukchi Sea and the northern Bering Sea of the western Arctic Ocean during the summer sea-ice reduction period (August 5 to August 24, 2016). A total of 44 ciliate species were identified, with seven species dominated the communities in the water column. Multivariate and univariate analyses demonstrated that: (1) community structures of ciliates vary significantly among eight water depths; (2) variations in the vertical distribution of ciliates were significantly correlated with changes in physicochemical variables, especially the ammonia; (3) the distributions of the three dominant species were significantly and positively related to the chlorophyll a and ammonia concentrations; and (4) species richness and abundance were significantly and positively correlated with the concentrations of ammonia and chlorophyll a.

Novel amine-functionalized iron trimesates with enhanced peroxidase-like activity and their applications for the fluorescent assay of choline and acetylcholine.

We herein describe novel amine-grafted metal-organic frameworks (MOFs) as a promising alternative to natural peroxidase enzyme and their applications for a fluorescent assay of choline (Cho) and acetylcholine (ACh). Among diverse amine-functionalized MOFs, N,N,N',N'-tetramethyl-1,4-butanediamine (TMBDA)-functionalized MIL-100(Fe) (TMBDA-MIL-100(Fe)) exhibited the highest peroxidase activity by developing intense fluorescence from Amplex UltraRed (AUR) in the presence of HO, which was presumably due to the synergetic effect of the enhanced negative potential and precisely controlled molecular size of the grafted diamine. Based on the excellent peroxidase-like activity of TMBDA-MIL-100(Fe), choline and ACh were reliably determined down to 0.

Isomeric Detergent Comparison for Membrane Protein Stability: Importance of Inter-Alkyl-Chain Distance and Alkyl Chain Length.

Membrane proteins encapsulated by detergent micelles are widely used for structural study. Because of their amphipathic property, detergents have the ability to maintain protein solubility and stability in an aqueous medium. However, conventional detergents have serious limitations in their scope and utility, particularly for eukaryotic membrane proteins and membrane protein complexes.

Mesitylene-Cored Glucoside Amphiphiles (MGAs) for Membrane Protein Studies: Importance of Alkyl Chain Density in Detergent Efficacy.

Detergents serve as useful tools for membrane protein structural and functional studies. Their amphipathic nature allows detergents to associate with the hydrophobic regions of membrane proteins whilst maintaining the proteins in aqueous solution. However, widely used conventional detergents are limited in their ability to maintain the structural integrity of membrane proteins and thus there are major efforts underway to develop novel agents with improved properties.

Adsorptive separation of xenon/krypton mixtures using a zirconium-based metal-organic framework with high hydrothermal and radioactive stabilities.

The separation of xenon/krypton mixtures is important for both environmental and industrial purposes. The potential of three hydrothermally stable MOFs (MIL-100(Fe), MIL-101(Cr), and UiO-66(Zr)) for use in Xe/Kr separation has been experimentally investigated. From the observed single-component Xe and Kr isotherms, isosteric heat of adsorption (Q), and IAST-predicted Xe/Kr selectivities, we observed that UiO-66(Zr) has the most potential as an adsorbent among the three candidate MOFs.

Novel Xylene-Linked Maltoside Amphiphiles (XMAs) for Membrane Protein Stabilisation.

Membrane proteins are key functional players in biological systems. These biomacromolecules contain both hydrophilic and hydrophobic regions and thus amphipathic molecules are necessary to extract membrane proteins from their native lipid environments and stabilise them in aqueous solutions. Conventional detergents are commonly used for membrane protein manipulation, but membrane proteins surrounded by these agents often undergo denaturation and aggregation.