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Journal ArticleDOI

Mixed matrix membranes with molecular-interaction-driven tunable free volumes for efficient bio-fuel recovery

TLDR
In this paper, the influence of the incorporation of POSS on the polymer structure was systematically studied by molecular dynamics simulations combined with DSC, XRD and IR measurements, and the results indicated that facilely incorporating POSS into PDMS by molecular interactions could manipulate favorable interfacial morphology and tunable free volumes in MMMs.
Abstract
Mixed matrix membranes (MMMs), consisting of inorganic fillers dispersed in a polymer matrix, are regarded as one of the most promising futuristic membranes. This work reports the utilization of molecular interactions to finely control the conformation and topology of polymer chains to fabricate high-performance polyhedral oligomeric silsesquioxanes (POSS)/polydimethylsiloxane (PDMS) MMMs. The influence of the incorporation of POSS on the polymer structure was systematically studied by molecular dynamics simulations combined with DSC, XRD and IR measurements. The surface and interfacial morphologies of the MMMs were observed through SEM, TEM and AFM characterizations. In particular, positron annihilation spectroscopy was employed to analyze the evolution of free volumes in the MMMs. Results indicated that facilely incorporating POSS into PDMS by molecular interactions could manipulate favorable interfacial morphology and tunable free volumes in MMMs. In the PDMS MMMs, the small free volumes were reduced and the large free volumes increased; these changes were beneficial for the preferential permeation of large-sized molecules through the polymeric membrane. As applied to the bio-butanol recovery from aqueous solutions, the prepared POSS/PDMS MMMs exhibited a simultaneous increase in permeability and selectivity, breaking the permeability-selectivity trade-off limitation, moreover transcending the upper bound of the state-of-the-art organophilic pervaporation membranes. Therefore, our work demonstrates that the proposed approach based on rationally creating molecular interactions can be expected to have broad applicability in fabricating high-quality MMMs for molecular separations.

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Citations
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Journal ArticleDOI

Ultrathin two-dimensional MXene membrane for pervaporation desalination

TL;DR: In this paper, the ultrathin 2D MXene membrane with thickness down to several tens of nanometers was developed for pervaporation desalination by stacking synthesized atomic-thin MXene nanosheets.
Journal ArticleDOI

UiO-66-polyether block amide mixed matrix membranes for CO2 separation

TL;DR: In this paper, the UiO-66-NH 2 nanoparticles were embedded into polyether block amide (PEBA) polymer membranes for CO 2 separation, and the improved dispersibility of the polymer matrix was demonstrated.
Journal ArticleDOI

Size effects of graphene oxide on mixed matrix membranes for CO2 separation

TL;DR: In this paper, the effects of GO lateral size on membranes morphologies, microstructures, physicochemical properties, and gas separation performances were systematically investigated, by varying the GO lateral sizes (100-200 nm, 1-2 μm, and 5-10 μm).
Journal ArticleDOI

High-performance multilayer composite membranes with mussel-inspired polydopamine as a versatile molecular bridge for CO2 separation.

TL;DR: PDA was selected as a versatile molecular bridge between hydrophobic PDMS and hydrophilic PVAm and exhibits a notably enhanced CO2 permeance combined with a slightly improved CO2/N2 selectivity, as well as superior structural stability.
References
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TL;DR: In this paper, a method is described to realize coupling to an external bath with constant temperature or pressure with adjustable time constants for the coupling, which can be easily extendable to other variables and to gradients, and can be applied also to polyatomic molecules involving internal constraints.
Journal ArticleDOI

A molecular dynamics method for simulations in the canonical ensemble

TL;DR: In this paper, a molecular dynamics simulation method which can generate configurations belonging to the canonical (T, V, N) ensemble or the constant temperature constant pressure ensemble was proposed, which is tested for an atomic fluid (Ar) and works well.
Journal ArticleDOI

Kinetics of Phase Change. II Transformation‐Time Relations for Random Distribution of Nuclei

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Journal ArticleDOI

COMPASS: An ab Initio Force-Field Optimized for Condensed-Phase ApplicationsOverview with Details on Alkane and Benzene Compounds

TL;DR: In this paper, a general all-atom force field for atomistic simulation of common organic molecules, inorganic small molecules, and polymers was developed using state-of-the-art ab initio and empirical parametrization techniques.
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