Adsorption Structure and Selectivity of Phenols in Water-Immersed Organomontmorillonite Investigated by Molecular Simulation.

The two-dimensional interlayer space of layered materials has been highlighted due to their adsorption property, whose nanostructure in the water-immersed state is scarcely understood by experiment. Recent developments in molecular simulation have enabled researchers to investigate the interlayer structure, but water content is necessary for accurate modeling. In the present study, we proposed a theoretical method to estimate the saturated water content and adsorption selectivity of trichlorophenol and phenol in montmorillonite modified with hexadecyltrimethylammonium ions.

Layered Silicates Exhibiting MOF-Like Gate-Opening Behaviors in Liquid-Phase Adsorptions: Experimental and Theoretical Investigations.

Layered silicates, including clay minerals, can be used as liquid-phase adsorbents in many important applications. However, because their two-dimensional interlayer space is narrow and not entirely opened due to the presence of interlayer species, guest species are forced to penetrate while expanding the interlayer space, which limits their adsorption performances compared with microporous materials such as MOFs and zeolites. Herein, as reported for the adsorption of gaseous species on flexible MOFs, we report a layered silicate that exhibits gate-opening adsorption in liquid phases.

Hydrophilicity of Organically Modified Montmorillonite and Effect on Benzene Adsorption by the Molecular Dynamics Method.

Interlayer modification of layered materials with organocations has been known to endow the nanocomposite with hydrophobicity, and adsorption of aromatic compounds in the aqueous phase has been investigated for decades by using montmorillonite, a representative layered clay mineral, as the host material. Usage of the organocation has been believed to be effective due to the π-π interaction with the aromatic adsorbate, the presence of which is not verified spectroscopically in the water-immersed state. Considering that the organocation is generally regarded as a pillar to keep the interlayer space, the interaction between the organocation and adsorbate has not yet been clarified sufficiently.

High Efficient CO Separation at High Pressure by Grain-Boundary-Controlled CHA Zeolite Membrane Investigated by Non-Equilibrium Molecular Dynamics.

The CO permeability and selectivity of CHA-type zeolite membranes in the separation of a CO/CH mixture gas at high pressure were evaluated using non-equilibrium molecular dynamics (NEMD). It was found that in a perfectly crystalline, defect-free CHA membrane, the adsorption of CH, which diffuses slowly in the pores, hinders CO permeation. Therefore, an increase in the amount of CH adsorbed at high pressure decreases the CO permeability and significantly reduces the CO selectivity of the CHA membrane.

Estimation of Adsorbed Amounts in Organoclay by Machine Learning.

Adsorption properties of organoclay have been investigated for decades focusing on the morphology and physicochemical properties of two-dimensional interlayers. Experimental studies have previously revealed that the adsorption mechanisms depend on the molecular species of the organocation and adsorbate, making it difficult to estimate the adsorbed amount without experiments. Considering that the adsorption of aromatic compounds has been reported by using various clays, organocations, and adsorbates, machine learning is a promising method to overcome the difficulty.

Solvent-Solute Interaction Effect on Permeation Flux through Forward Osmosis Membranes Investigated by Non-Equilibrium Molecular Dynamics.

The relationship between the solvent-solute interaction and permeation properties is fundamental in the development of the forward osmosis (FO) membrane. In this study, we report on the quantitative reproduction of the permeation flux, which has different solvent-solute interactions, through the modeled FO membrane by non-equilibrium molecular dynamics (NEMD). The interaction effect was investigated by changing the interatomic interaction between the solute and the solvent.

Intercalation-Induced Ordered Nanostructure in the Interlayer Modified with Methylviologen by Molecular Dynamics Simulation.

Intercalation of phenol in montmorillonite, a representative layered material, has historically been investigated, and modification of the interlayer with methylviologen (Mont-MV) results in color change due to formation of a charge-transfer complex. Its detailed nanostructure, however, has yet been revealed owing to its small gallery height and poor crystallinity. In the present study, we performed molecular dynamics simulation to investigate structural changes in Mont-MV by the intercalation of phenol.

Inhomogeneity of Organically Modified Montmorillonite Revealed by Molecular Dynamics Simulation.

The modification of an interlayer of layered materials by intercalation with an organoammonium ion has been a promising method to control the polarity of the two-dimensional nanospace. Montmorillonite is one of the best-known examples, and the modification with octadecyltrimethylammonium ion (Mont-C) results in adsorption of anthracene and pyrene together with specific excimer emission, while the nanostructure is yet to be uncovered at the molecular level because the gallery height is only ca. 27 Å.

Electrically Induced Alignment of Semiconductor Nanosheets in Niobate-Clay Binary Nanosheet Colloids toward Significantly Enhanced Photocatalysis.

Aqueous binary colloids of niobate and clay nanosheets, prepared by the exfoliation of their mother layered crystals, are unique colloidal systems characterized by the separation of niobate and clay nanosheet phases, where niobate nanosheets form liquid crystalline domains with the size of several tens of micrometers among isotropically dispersed clay nanosheets. The binary colloids show unusual photocatalytic reactions because of the spatial separation of photocatalytically active niobate and photochemically inert clay nanosheets. The present study shows structural conversion of the binary colloids with an external electric field, resulting in the onsite alignment of colloidal nanosheets to improve the photocatalytic performance of the system.

Aqueous synthesis of protectant-free copper nanocubes by a disproportionation reaction of CuO on synthetic saponite.

Here, we report a synthesis of Cu nanocubes by photoreduction of CuSO4. Because synthetic saponite (one of the layered clay minerals) was used as the adsorbent, the nanocubes contained no capping agents or protectants, and the disproportionation reaction of Cu2O with H2SO4 was found to be the key for morphological control.