Anisotropic Dynamics of Binary Particles in Confined Geometries.

The diffusion dynamics of colloidal particles in a good solvent confined between two parallel quartz walls have been studied within the framework of dynamical density functional theory. The highly ordered density layers induced by interfacial effects give rise to the oscillating dynamics, resulting in position-dependent structural relaxations and diffusivities. Further investigation reveals that particle size, particle-wall interaction, and slitpore width play different roles in affecting the oscillating behaviors along different directions. As a result, the theory yields the local mean square displacements in perpendicular and parallel directions, which agree remarkably well with prior experimental measurements. The results indicate that the mean square displacements can be quantitatively predicted based on the knowledge of inhomogeneous thermodynamics and dynamics. The local and averaged free energy evolution of the binary particles has been described and presented to understand their dynamic mechanism in confined geometry.

The mechanism of roughness-induced CO2 microbubble nucleation in polypropylene foaming.

Within the framework of classical density functional theory, the thermodynamic driving forces for CO2 microbubble nucleation have been quantitatively evaluated in the foaming of polypropylene containing amorphous and crystalline structures. After the addition of fluorinated polyhedral oligomeric silsesquioxane particles into the polypropylene matrix, we construct different composite surfaces with nanoscale roughness for bubble nucleation. Meanwhile, as the dissolved CO2 molecules increase, the corresponding CO2/PP binary melts can be formulated in the systems. Due to the roughness effect coupled with the weak interactions of particle-PP, PP chains in the binary melts are depleted from the surfaces, leading to a significant enhancement of osmotic pressure in depletion regions. During the foaming process, a large number of dissolved CO2 molecules are squeezed into the regions, thus local supersaturations are dramatically improved, and the energy barriers for bubble nucleation are dramatically reduced. Moreover, when the nanocomposite surfaces display ordered nanoscale patterns, the energy barriers can be further reduced to their respective minimum values, and the bubble number densities reach their maximum. Accordingly, the bubble number densities can be enhanced by 4 or 5 orders of magnitude for bubbles nucleated on the crystalline or amorphous PP nanocomposite surface. In contrast, when the foaming pressure is increased from 15 to 20 MPa, the elevated bubble number density in the foaming PP matrix is less than one order of magnitude. As a result, the enhancement of local supersaturation induced by the controlled nanoscale roughness is much more effective than that of bulk supersaturation given by high pressure.

Understanding Controls on Wetting at Fluorinated Polyhedral Oligomeric Silsesquioxane/Polymer Surfaces.

Fluorinated polyhedral oligomeric silsesquioxane (F-POSS) nanoparticles have been widely used to enhance the hydrophobicity or oleophobicity of polymer films via constructing the specific micro/nanoscale roughness. In this work, we study the oleophobicity of pure and F-POSS-decorated poly(vinylidene fluoride) (PVDF) and poly(methyl methacrylate) (PMMA) films using a dynamic density functional theory approach. The role of nanoparticle size and coverage and the chemical features of F-POSS and the polymer film in the wetting behavior of diiodomethane droplets has been integrated to the remaining ratio of surface potential to quantitatively characterize the corner effect. It is shown that, on the basis of universal force field parameters, the theoretically predicted contact angles are in general agreement with the available experimental data.

Control of Uniform and Interconnected Macroporous Structure in PolyHIPE for Enhanced CO2 Adsorption/Desorption Kinetics.

The highly uniform and interconnected macroporous polymer materials were prepared within the high internal phase hydrosol-in-oil emulsions (HIPEs). Impregnated with polyethylenimine (PEI), the polyHIPEs were then employed as solid adsorbents for CO2 capture. Thermodynamic and kinetic capture-and-release tests were performed with pure CO2, 10% CO2/N2, and moist CO2, respectively. It has shown that the polyHIPE with suitable surface area and PEI impregnation exhibits high CO2 adsorption capacity, remarkable CO2/N2 selectivity, excellent adsorption/desorption kinetics, enhanced efficiency in the presence of water, and admirable stability in capture and release cycles. The results demonstrate the superior comprehensive performance of the present PEI-impregnated polyHIPE for CO2 capture from the postcombustion flue gas.

Diffusive dynamics of polymer chains in an array of nanoposts.

We present a dynamic density functional approach to study polymer chain diffusion in a good solvent in the confinement of a nanopost array. Three key results emerge from our study. First, we show different scaling laws of the chains moving toward, close to, and around the posts. Second, in the flux process of polymer chains, the head, side, and middle segments display different scaling laws. As the chains come in contact with the posts, an enlarged motion discrepancy emerges between the head and middle segments perpendicular to the posts. For instance, the motion of head segments transforms from Zimm to reputation type, whereas the middle segments almost retain the Zimm motion. Third, as the spacing crack between two posts narrows down, a climbing effect along the posts can be clearly observed in the polymer motion.

Effect of chain topology of polyethylenimine on physisorption and chemisorption of carbon dioxide.

Polyethylenimine (PEI) is a promising candidate for CO2 capture. In this work, the physisorption and chemisorption of CO2 on various low-molecular-weight PEIs are investigated to identify the effect of chain architecture on sorption. The reliability of theoretical calculations are partially supported by our experimental measurements. Physisorption is calculated independently by the reference interaction-site model integral equation theory; chemisorption is distinguished from the total sorption given by the quantum density functional theory. It is shown that, as the chain length increases, both chemisorption and physisorption drop off nonlinearly, but the decay amplitude of chemisorption is more apparent. Conversely, as the amine group approaches the central triamine unit of each oligomer, the sorption capacity decreases, affecting the sorption equilibrium in a complex way. This arises from the cooperative contribution of an increased steric effect and renormalized electronic distribution.

Evaluation of macroscale wetting equations on a microrough surface.

The wettability of critical droplets on microscale geometric rough surfaces has been investigated using a density functional theory approach. In order to analyze the effect of roughness on nucleation free-energy barriers, the local density fluctuations at liquid-solid interfaces induced by the multi-interactions of a corner substrate are presented to interpret the interfacial free-energy variations, and the vapor-liquid-solid contact line tensions are derived from the contact angles of nuclei to account for the three-phase contact energies. The corresponding wetting diagrams have been constructed in Cassie, Wenzel, and impregnation regions. It is shown that, under the same condition, modest deviations between the microscale and the macroscale models can be observed within the Cassie region, whereas these deviations have been enlarged in the Wenzel and impregnation regions as well as the Cassie-Wenzel transition region. These deviations are also correlated to the roughness of the surface. The reason can be attributed to the cooperative effect of the liquid-solid interfacial free energy and line tension. This study offers a fundamental understanding of wettability of ultrasmall droplets on a microscale geometric rough surface.

Understanding the microstructure of particle dispersion in confined copolymer nanocomposites.

The microstructures of diblock copolymer/particle composites confined in slitpores have been investigated using a density functional theory approach. It has been shown that, under the condition of confinement, particles display different distributions near the solid surfaces, in the microdomains of two blocks, and at the microphase interfaces. The final dispersion depends on the balance between the enthalpic contribution arising from the particle-segment attraction as well as the entropy-driven depletion attraction induced by the polymer conformation and the confinement environment. For the systems in which particles weakly attract one block but repel another block, particle dispersion can be enhanced by the increasing confinement effect, and the enhancement becomes more obvious as the size asymmetries of particles and two blocks increase. If the attraction increases, however, particle dispersion declines as the confinement effect increases.

Role of block copolymer morphology on particle percolation of polymer nanocomposites.

In this study, the effects of nanoparticle volume fraction, block stiffness, and diblock composition on the microstructure and electrical properties of composites are investigated using molecular dynamics simulation. It is shown that selective localization of conductive nanoparticles in a continuous block of diblock copolymer can dramatically reduce the percolation threshold. In the flexible-flexible copolymer systems with a relatively low particle loading, as the ratio of two blocks varies, one sees four kinds of phase structure: signal continuous, lamellar, co-continuous, and dispersed, corresponding to the order-disorder and continuity-dispersion transitions. In consideration of particle connectivity, the best electrical performance can be achieved with a special tri-continuous microstructure. While in the semi-flexible systems, the existence of rigid blocks can destroy the lamellar structure. If particles are located in the flexible block, a moderate stiffness of the rigid block can extensively enlarge the tri-continuous region, and high conductivity can be realized over a wide range of diblock compositions. If particles are located in the rigid block, however, high conductivity only emerges in a narrow composition range. In addition, the block should be prevented from becoming overstiff because this will cause direct particle aggregation.

Theoretical insights into nucleation of CO2 and CH4 hydrates for CO2 capture and storage.

We present a hybrid three-dimensional (3D) theoretical approach, the density functional theory (DFT) integrated with the reference interaction site model (RISM), to investigate the nucleation of CO2 and CH4 hydrates. Within the theoretical framework, the 3D-RISM is applied to describe gas density distributions in hydrate cages, and the 3D-DFT is used to describe the interfacial structure and properties of the two hydrates, as well as their nucleation. The crystal-liquid phase equilibria of CO2 and CH4 hydrates are predicted by the hybrid 3D-DFT-RISM, and compared with the available experimental data to examine the theoretical model. In particular, the local and interfacial structure and properties, the critical nucleus radii and free-energy barriers at moderate concentration supersaturation are presented to analyze their nucleation. The formation enthalpies for the two hydrates are calculated to evaluate the possibility of CO2 storage by CH4-CO2 replacement in hydrate.

Density functional theory for carbon dioxide crystal.

We present a density functional approach to describe the solid-liquid phase transition, interfacial and crystal structure, and properties of polyatomic CO2. Unlike previous phase field crystal model or density functional theory, which are derived from the second order direct correlation function, the present density functional approach is based on the fundamental measure theory for hard-sphere repulsion in solid. More importantly, the contributions of enthalpic interactions due to the dispersive attractions and of entropic interactions arising from the molecular architecture are integrated in the density functional model. Using the theoretical model, the predicted liquid and solid densities of CO2 at equilibrium triple point are in good agreement with the experimental values. Based on the structure of crystal-liquid interfaces in different planes, the corresponding interfacial tensions are predicted. Their respective accuracies need to be tested.

Density functional theory for crystal-liquid interfaces of Lennard-Jones fluid.

A density functional approach is presented to describe the crystal-liquid interfaces and crystal nucleations of Lennard-Jones fluid. Within the theoretical framework, the modified fundamental measure theory is applied to describe the free energy functional of hard sphere repulsion, and the weighted density method based on first order mean spherical approximation is used to describe the free energy contribution arising from the attractive interaction. The liquid-solid equilibria, density profiles within crystal cells and at liquid-solid interfaces, interfacial tensions, nucleation free energy barriers, and critical cluster sizes are calculated for face-centered-cubic and body-centered-cubic nucleus. Some results are in good agreement with available simulation data, indicating that the present model is quantitatively reliable in describing nucleation thermodynamics of Lennard-Jones fluid.

Evolution of conductive network and properties of nanorod/polymer composite under tensile strain.

In this work, the conductive network, probability, and percolation threshold of nanorod/polymer composites under tensile strain are investigated using the molecular dynamics simulation. The internal interactions, including polymer-polymer, polymer-nanorod, and nanorod-nanorod interactions, are taken into account in simulations. In particular, the influence of polymer induced depletion force on the orientation of nanorods is analyzed. Under a constant strain, the conductive stability firstly declines and then rises with the increasing concentration of fillers, and the minimum corresponds to the percolation threshold. As strain increases, the result exhibits a strong anisotropy in the stability of conductive property.

Engineering of Defective MOF-801 Nanostructures within Macroporous Spheres for Highly Efficient and Stable Water Harvesting.

Water harvesting using the metal-organic framework (MOF)-801 is restricted by limited working capacity, powder structuring, and finite stability. To overcome these issues, MOF-801 is crystallized on the surface of macroporous poly(N-isopropylacrylamide-glycidyl methacrylate) spheres, called P(NIPAM-GMA), through an in situ confined growth strategy, forming spherical MOF-801@P(NIPAM-GMA) composite with temperature-responsive function. By lowering the nucleation energy barrier, the average size of the MOF-801 crystals decreases by 20 times. Thus, abundant defects as adsorption sites for water can be installed in the crystals lattices. As a consequence, the composite provides an unprecedented high water harvesting efficiency. The composite is produced in the kilogram-scale and can capture 1.60 kg H2 O/kg composite/day from 20% relative humidity between 25 and 85 °C. This study provides an effective methodology for improving the adsorption capacity through controlled defects formation as adsorption sites and to improve the kinetics through the design of a composite with macroporous transport channel network.

Modified PRISM theory for confined polymers.

We propose a modified polymer reference interaction site model (PRISM) to describe the interfacial density profiles of polymers in contact with planar and curved solid surfaces. In the theoretical approach, a bridge function derived from density functional method is included. In description of hard-sphere polymer at planar and curved surfaces with an arbitrary external field, the effect of modification has been validated by the available simulation data, except for low density system. When extended to confined real systems, the modified theoretical model also shows an encouraging prospect in description of the interfacial structure and properties.

Wetting behavior of spherical nanoparticles at a vapor-liquid interface: a density functional theory study.

The wetting behavior of spherical nanoparticles at a vapor-liquid interface is investigated by using density functional theory, and the line tension calculation method is modified by analyzing the total energy of the vapor-liquid-particle equilibrium. Compared with the direct measurement data from simulation, the results reveal that the thermodynamically consistent Young's equation for planar interfaces is still applicable for high curvature surfaces in predicting a wide range of contact angles. The effect of the line tension on the contact angle is further explored, showing that the contact angles given by the original and modified Young's equations are nearly the same within the region of 60° < θ < 120°. Whereas the effect is considerable when the contact angle deviates from the region. The wetting property of nanoparticles in terms of the fluid-particle interaction strength, particle size, and temperature is also discussed. It is found that, for a certain particle, a moderate fluid-particle interaction strength would keep the particle stable at the interface in a wide temperature range.

A theoretical study of structure-solubility correlations of carbon dioxide in polymers containing ether and carbonyl groups.

This work involves a theoretical study to investigate the effects of the structure on CO(2) sorption in polymers, where poly(ethylene oxide) (PEO), poly(propylene oxide) (PPO), poly(vinyl acetate) (PVAc), poly(ethylene carbonate) (PEC) and poly(propylene carbonate) (PPC) were examined. In the theoretical approach, the multi-site semiflexible chain model and the renormalized technique of electrostatic potentials were incorporated into the polymer reference interaction site model (PRISM). To test the theory, molecular dynamic simulations were performed using the TraPPE-UA force field. The theoretically calculated reduced X-ray scattering intensities and intermolecular correlation functions of these five polymers are found to be in qualitative agreement with the corresponding molecular simulation data. The theory was then employed to investigate the distribution functions between CO(2) and different sites of the polymers with consideration of the Lennard-Jones, potential of mean force, and columbic contributions. Based on the detailed structure characteristics of CO(2) in contact with different groups, the CO(2) coordination molecular numbers were obtained and their sorption intensities analyzed. Finally, the sorption isotherms of CO(2) in these five polymers were calculated. The results for PEO, PPO and PVAc are close to the available experimental curves, and the trend of CO(2) solubility is PPC > PEC > PVAc ~ PPO > PEO.

Preparation of medical hydrophilic and antibacterial silicone rubber via surface modification.

Bacterial adhesion of medical indwelling devices shortens their service life and brings about infections in patients. The combination of hydrophilic and antibacterial modifications can not only kill the bacteria in contact with the surface, but also avoid the adhesion of dead bacteria. From this view, with a self-made quaternary ammonium salt and a zwitterion as the modifiers, a modified silicone rubber, SR-g-(DMAPS-co-QA), was prepared via random co-grafting. The static water angle test and antibacterial assays proved the enhancement of both the hydrophilicity and antibacterial activity. In addition, compared with the unmodified silicone rubber, after 7 days of co-cultivation in E. coli suspension, SR-g-(DMAPS-co-QA) demonstrated good resistance to biofilm formation. Furthermore, to simulate the real situation, its antibacterial effect in dynamic flow condition was measured, confirming that SR-g-(DMAPS-co-QA) still maintained good antibacterial performance after a 48 hour cyclic flow of E. coli bacterial suspension.

A Highly Efficient and Stable Composite of Polyacrylate and Metal-Organic Framework Prepared by Interface Engineering for Direct Air Capture.

We present a kilogram-scale experiment for assessing the prospects of a novel composite material of metal-organic framework (MOF) and polyacrylates (PA), namely NbOFFIVE-1-Ni@PA, for trace CO2 capture. Through the interfacial enrichment of metal ions and organic ligands as well as heterogeneous crystallization, the sizes of microporous NbOFFIVE-1-Ni crystals are downsized to 200-400 nm and uniformly anchored on the macroporous surface of PA via interfacial coordination, forming a unique dual-framework structure. Specifically, the NbOFFIVE-1-Ni@PA composite with a loading of 45.8 wt % NbOFFIVE-1-Ni yields a superior CO2 uptake (ca. 1.44 mol·kg-1) compared to the pristine NbOFFIVE-1-Ni (ca. 1.30 mol·kg-1) at 400 ppm and 298 K, indicating that the adsorption efficiency of NbOFFIVE-1-Ni has been raised by 2.42 times. Meanwhile, the time cost for realizing a complete adsorption/desorption cycle in a fluidized bed has been shortened to 25 min, and the working capacity (ca. 0.84 mol·kg-1) declines only by 1.3% after 2000 cycles. The device is capable of harvesting 2.1 kg of CO2 per kilogram of composite daily from simulated air with 50% relatively humidity (RH). To the best of our knowledge, the excellent adsorption/desorption performances of NbOFFIVE-1-Ni@PA position it as the most advantageous and practically applicable candidate for trace CO2 capture.

Quaternary tannic acid with improved leachability and biocompatibility for antibacterial medical thermoplastic polyurethane catheters.

The surfaces of indwelling catheters offer sites for the adherence of bacteria to form biofilms, leading to various infections. Therefore, the development of antibacterial materials for catheters is imperative. In this study, combining the strong antibacterial effect of a quaternary ammonium salt (QAS) and the high biocompatibility of tannic acid (TA), we prepared a quaternary tannic acid (QTA) by grafting a synthesized quaternary ammonium salt, dimethyl dodecyl 6-bromohexyl ammonium bromide, onto TA. To prepare antibacterial catheters, QTA was blended with thermoplastic polyurethane (TPU) via melt extrusion, which is a convenient and easy-to-control process. Characterization of the TPU blends showed that compared with those of the QAS, dissolution rate and biocompatibility of QTA were significantly improved. On the premise that the introduction of QTA had only a slight effect on the original mechanical properties of pristine TPU, the prepared TPU/QTA maintained satisfactory antibacterial activities in vitro, under a flow state, as well as in vivo. The results verified that the TPU/QTA blend with a QTA content of 4% is effective, durable, stable, and non-toxic, and exhibits significant potential as a raw material for catheters.