Engineering of Interfacial Energy Bands for Synthesis of Photoluminescent 0D/2D Coupled MOF Heterostructure with Enhanced Selectivity toward the Proton-Exchange Membrane.

Engineering of the interface for tuning the structural, functional, and electronic properties of materials via the formation of heterostructure composites exhibits immense potential in the current research scenario. This study reports a novel ternary composite synthesized by decoration of zero-dimensional Pd nanoparticles (NPs) and two-dimensional (2D) graphite oxide (GO) sheets in the UiO-66 metal-organic framework (MOF). A mixed matrix membrane was fabricated by incorporating this composite in the SPEEK polymer matrix, which exhibited higher selectivity compared to commercial Nafion 117.

Loading and release of doxorubicin hydrochloride from iron(iii) trimesate MOF and zinc oxide nanoparticle composites.

A significant amount of work has been done in recent years for the development of metal organic framework (MOF) based drug delivery vehicles. Often, nanomaterials such as iron oxide (Fe3O4), zinc oxide (ZnO), and other metal oxides like graphene oxide etc. are incorporated into the structures to impart additional functionality.

Effect of adsorbent history on adsorption characteristics of MIL-53(Al) metal organic framework.

Structural transformation of MIL-53(Al) metal organic framework from large pore to narrow pore form (lp → np) or vice versa is known to occur by adsorption of certain guest molecules, by temperature change or by applying mechanical pressure. In this work, we perform a systematic investigation to demonstrate that adsorbent history also plays a decisive role in the structural transitions of this material (and hence on its adsorption characteristics). By changing the adsorbent history, parent MIL-53(Al) is tuned into its np domain at ambient temperature such that it not only exhibits a significant increase in CO2 capacity, but also shows negligible uptake for CH4, N2, CO, and O2 at subatmospheric pressure.

Net adsorption: a thermodynamic framework for supercritical gas adsorption and storage in porous solids.

The thermodynamic treatment of adsorption phenomena is based on the Gibbs dividing surface, which is conceptually clear for a flat surface. On a flat surface, the primary extensive property is the area of the solid. As applications became more significant, necessitating microporous solids, early researchers such as McBain and Coolidge implemented the Gibbs definition by invoking a reference state for microporous solids.

Temperature-dependent pyrolytic product evolution profile for low-density polyethylene from gas chromatographic study.

In this work, a product distribution study from thermal degradation of low-density polyethylene (LDPE) is presented. Thermal degradation of the polymer was investigated under dynamic condition in an inert environment using a thermo-gravimetric analyzer (TGA) coupled with evolved products' analysis using a gas chromatograph (GC). Fractions evolved at nine different temperatures from 200 to 600 degrees C were injected into GC for a detailed product analysis.