Construction and Adsorption Performance Study of GO-CNT/Activated Carbon Composites for High Efficient Adsorption of Pollutants in Wastewater.

Based on the increasing application requirements for the efficient adsorption of wastewater pollutants, graphene oxide-carbon nanotube/activated carbon (GO-CNT/AC) composites are constructed from the optimal microstructure matching of GO, CNTs, and AC materials by solution impregnation and freeze-drying methods. Three-dimensional structures with nano-micro hierarchical pores are established, with GO and CNTs uniformly dispersed on the AC surface, effectively restrain the agglomeration. The added CNTs played a "spring" role, supporting the gap between the GO sheets and AC matrix. Meanwhile, stable links are formed between GO, CNTs, and AC, realizing the synergistic matching of the microstructure, which provides abundant active absorption sites beneficial for improving the adsorption performance. The influences of the CNT contents, adsorbent amounts, methylene blue (MB) concentrations, and pH values on the adsorption property of GO-CNT/AC composites are systematically investigated. The results show that when the pH value of the MB solution is 13, the CNT concentration is 3 mg/mL and the MB concentration is 200 mg/L, the adsorption property of the composite is the best, with an adsorption capacity of 190.8 mg/g and a removal percentage of 95.4%. Compared with the raw AC, the adsorption capacity and removal percentage of the composites are increased by 73.9% and 72.8%, respectively. The GO-CNT/AC composites exhibit excellent cyclic adsorption performance, with a cyclic stability of 91.8% after six rounds of adsorption-desorption cycles. The kinetic analysis shows that the adsorption process conforms to the PSO kinetic model. By fitting of the IPD model, the adsorption mechanisms of the GO-CNT/AC composites are divided into two adsorption stages and described respectively. This study provides a new way to achieve highly efficient adsorption of pollutants in wastewater.

Preparation and Adsorption Performance Study of Graphene Quantum Dots@ZIF-8 Composites for Highly Efficient Removal of Volatile Organic Compounds.

Based on the large specific surface area and excellent adsorption potential of graphene quantum dots (GQDs) and zeolitic imidazolate framework-8 (ZIF-8) materials, a GQDs@ZIF-8 composite was constructed to achieve optimal matching of the microstructure and to acquire efficient adsorption of volatile organic compounds (VOCs). GQDs and ZIF-8 were synthesized and then compounded by the solution co-deposition method to obtain GQDs@ZIF-8 composites. GQDs were uniformly decorated on the surface of the ZIF-8 metal-organic framework (MOF), effectively restraining the agglomeration, improving the thermal stability of ZIF-8 and forming abundant active sites. Thus, the VOC removal percentage and adsorption capacity of the GQDs@ZIF-8 composites were significantly improved. Toluene and ethyl acetate were chosen as simulated VOC pollutants to test the adsorption performance of the composites. The results showed that, after the addition of GQDs, the adsorption property of GQDs@ZIF-8 composites for toluene and ethyl acetate was obviously improved, with maximum adsorption capacities of 552.31 mg/g and 1408.59 mg/g, respectively, and maximum removal percentages of 80.25% and 93.78%, respectively, revealing extremely high adsorption performance. Compared with raw ZIF-8, the maximum adsorption capacities of the composites for toluene and ethyl acetate were increased by 53.82 mg/g and 104.56 mg/g, respectively. The kinetics and isotherm study revealed that the adsorption processes were in accordance with the pseudo-first-order kinetic model and the Freundlich isotherm model. The thermodynamic results indicated that the adsorption process of the GQDs@ZIF-8 composites was a spontaneous, endothermic and entropy increase process. This study provides a new way to explore MOF-based adsorption materials with high adsorption capacity which have broad application prospects in VOC removal fields.

Largely enhanced dielectric constant of PVDF nanocomposites through a core-shell strategy.

Core-shell structured TiO2@carbon nanowire (TiO2@C NW) hybrids with different carbon shell thicknesses were synthesized by a combination of a hydrothermal reaction and the chemical vapor deposition (CVD) method. Pristine TiO2 NWs with a high aspect ratio were obtained by a hydrothermal reaction and the as-synthesized TiO2 NWs were subsequently employed as the template for carbon shell deposition during the CVD procedure. The obtained TiO2@C NW hybrids have a uniform carbon shell and the thickness of the carbon shell could be precisely designed from 4 nm to 40 nm by controlling the deposition time. With the help of solution and melt blending methods, the TiO2@C NW hybrids were subsequently incorporated into the PVDF matrix to fabricate TiO2@C NWs/PVDF nanocomposites, which exhibit a similar percolative dielectric behavior to that reported in other percolative nanocomposites. Moreover, the dielectric properties of the TiO2@C NWs/PVDF nanocomposites could be accurately adjusted by tuning the carbon shell thickness of the TiO2@C NW hybrids. The highest dielectric constant (2171) of the TiO2@C NWs/PVDF nanocomposites is 80 times larger than those of the pristine TiO2-filled ones at the same filler loading, and 241 times higher than that of the pure PVDF matrix. The enhanced dielectric performance could be attributed to the improved interfacial polarizations of TiO2/C and C/PVDF interfaces. This approach provides an interesting alternative to fabricate high-performance dielectric nanocomposites for practical applications in the electronic industry.

Carbon Coated Boron Nitride Nanosheets for Polymer Nanocomposites with Enhanced Dielectric Performance.

Carbon coated boron nitride nanosheets (BNNSs@C) hybrids with different carbon contents were synthesized by a chemical vapor deposition (CVD) method. The content of carbon in as-obtained BNNSs@C hybrids could be precisely adjusted from 2.50% to 22.62% by controlling the carbon deposition time during the CVD procedure. Afterward, the BNNSs@C hybrids were subsequently incorporated into the polyvinylidene fluoride (PVDF) matrix to fabricate the BNNSs@C/PVDF nanocomposites through a combination of solution and melting blending methods. The dielectric properties of the as-obtained BNNSs@C/PVDF nanocomposites could be accurately tuned by adjusting the carbon content. The resultant nanocomposites could afford a high dielectric constant about 39 (10³ Hz) at BNNSs@C hybrids loading of 30 vol %, which is 4.8 times larger than that of pristine BNNSs-filled ones at the same filler loading, and 3.5 times higher than that of pure PVDF matrix. The largely enhanced dielectric performance could be ascribed to the improved interfacial polarizations of BNNSs/carbon and carbon/PVDF interfaces. The approach reported here offers an effective and alternative method to fabricate high-performance dielectric nanocomposites, which could be potentially applied to the embedded capacitors with high dielectric performance.

Influences of Thermal Treatment on the Dielectric Performances of Polystyrene Composites Reinforced by Graphene Nanoplatelets.

Dielectric properties of composites near percolation threshold (fc) are often sensitive to thermal treatments, and the annealing temperature is usually associated with a polymer's rheological properties. In this study, the influences of the thermal treatment on dielectric properties are investigated for the polystyrene (PS) matrix composite reinforced by graphene nanoplatelets (GNP) fillers near fc. It can be found that the thermal treatment can not only increase the dielectric constant, but also decrease the dielectric loss for the PS/GNP composite. This interesting phenomenon possibly happens in the interfacial region of PS/GNP with the thickness about 4-6 nm according to the electron energy-loss spectroscopy (EELS) results. The free volumes around the interface can be easily altered by the movement of polymeric segments after annealing at the glass transition temperature.

Design of Electrically Conductive Structural Composites by Modulating Aligned CVD-Grown Carbon Nanotube Length on Glass Fibers.

Function-integration in glass fiber (GF) reinforced polymer composites is highly desired for developing lightweight structures and devices with improved performance and structural health monitoring. In this study, homogeneously aligned carbon nanotube (CNT) shell was in situ grafted on GF by chemical vapor deposition (CVD). It was demonstrated that the CNT shell thickness and weight fraction can be modulated by controlling the CVD conditions. The obtained hierarchical CNTs-GF/epoxy composites show highly improved electrical conductivity and thermo-mechanical and flexural properties. The composite through-plane and in-plane electrical conductivities increase from a quasi-isolator value to ∼3.5 and 100 S/m, respectively, when the weight fraction of CNTs grafted on GF fabric varies from 0% to 7%, respectively. Meanwhile, the composite storage modulus and flexural modulus and strength improve as high as 12%, 21%, and 26%, respectively, with 100% retention of the glass transition temperature. The reinforcing mechanisms are investigated by analyzing the composite microstructure and the interfacial adhesion and wetting properties of CNTs-GF hybrids. Moreover, the specific damage-related resistance variation characteristics could be employed to in situ monitor the structural health state of the composites. The outstanding electrical and structural properties of the CNTs-GF composites were due to the specific interfacial and interphase structures created by homogeneously grafting aligned CNTs on each GF of the fabric.

Influence of Thermal Treatments on the Evolution of Conductive Paths in Carbon Nanotube-Al2O3 Hybrid Reinforced Epoxy Composites.

The conductive path formed by carbon nanotubes (CNTs) in a polymer matrix is one of the most attractive topics for developing multifunctional nanocomposites. In this article, we studied the evolution of conductive paths and interactions in the interfacial regions in epoxy-based composites reinforced by an urchinlike hybrid of CNTs and alumina microparticles (µAl2O3). A homogeneous dispersion of CNTs in the epoxy matrix was achieved thanks to the core-shell structures of CNTs-µAl2O3 hybrids, resulting in the interpenetrated epoxy's cross-linking network that strongly bonds with CNTs. Furthermore, thermal treatments at different temperatures around the glass-transition temperature (Tg) were conducted under vacuum on composites near the percolation threshold. It was found that the dielectric behavior and the Tg were shifted in spite of the constant CNT mass fraction used. This was mainly due to the fact that thermal treatment generated the adjustment of the cross-linking network of epoxy, and the distances between adjacent CNTs were reduced gradually. This study can provide insight into the evolution of conductive paths in the interfacial regions from a more straightforward perspective.

Quantitative Study of Interface/Interphase in Epoxy/Graphene-Based Nanocomposites by Combining STEM and EELS.

A quantitative study of the interphase and interface of graphene nanoplatelets (GNPs)/epoxy and graphene oxide (GO)/epoxy was carried out by combining scanning transmission electron microscopy (STEM) and electron energy-loss spectroscopy (EELS). The interphase regions between GNPs and epoxy matrix were clearly identified by the discrepancy of the plasmon peak positions in the low energy-loss spectra due to different valence electron densities. The spectrum acquisitions were carried out along lines across the interface. An interphase thickness of 13 and 12.5 nm was measured for GNPs/epoxy and GO/epoxy, respectively. The density of the GNPs/epoxy interphase was 2.89% higher than that of the epoxy matrix. However, the density of the GO/epoxy interphase was 1.37% lower than that of the epoxy matrix. The interphase layer thickness measured in this work is in good agreement with the transition layer theory, which proposed an area with modulus linearly varying across a finite width. The results provide an insight into the interphase for carbon-based polymer composites that can help to design the functionalization of nanofillers to improve the composite properties.

Versatile Wafer-Scale Technique for the Formation of Ultrasmooth and Thickness-Controlled Graphene Oxide Films Based on Very Large Flakes.

We present a new strategy to form thickness-adjusted and ultrasmooth films of very large and unwrinkled graphene oxide (GO) flakes through the transfer of both hemispherical and vertical water films stabilized by surfactants. With its versatility in terms of substrate type (including flexible organic substrates) and in terms of flake density (from isolated flakes to continuous and multilayer films), this wafer-scale assembly technique is adapted to a broad range of experiments involving GO and rGO (reduced graphene oxide). We illustrate its use through the evaluation of transparent rGO electrodes.

One-pot synthesis of Ag/r-GO/TiO2 nanocomposites with high solar absorption and enhanced anti-recombination in photocatalytic applications.

In this paper, we reported a simple one-pot solvothermal approach to fabricate Ag/reduced graphene oxide (r-GO)/TiO2 composite photocatalyst under atmospheric pressure. Based on the experimental data, we concluded that the introduction of Ag into classical graphene-TiO2 system (i) efficiently enlarges the absorption range, (ii) improves photogenerated electron separation and (iii) increases photocatalysis reaction sites. The optimized sample exhibits prominent photocatalysis ability as compared to pure TiO2 under simulated sunlight. We further proposed that besides the above three advantages of Ag, a different size of Ag nanoparticles is also responsible for the improved photocatalysis ability, where small size Ag nanoparticles (2-5 nm) could store a photoexcited electron that was generated from TiO2, while large-size Ag nanoparticles could utilize visible light due to their localized surface plasmon resonance (LSPR) absorption. Our present work gives new insights into the photocatalysis mechanism of noble metal/r-GO/TiO2 composites and provides a new pathway into the design of TiO2-based photocatalysts and promote their practical application in various environmental and energy issues.

Characterization of molecular recognition of phosphoinositide-3-kinase α inhibitor through molecular dynamics simulation.

Phosphatidylinositol 3-kinase α (PI3Kα) is a promising target for anticancer drug discovery due to its overactivation in tumor cells. To systematically investigate the interactions between PI3Kα and PIK75 which is the most selective PI3Kα inhibitor reported to date, molecular docking, molecular dynamics simulation, and ensuing energetic analysis were utilized. The binding free energy between PI3Kα and PIK75 is -10.04 kcal•mol(-1) using MMPBSA method, while -13.88 kcal•mol(-1) using MMGBSA method, which is beneficial for the binding. The van der Waals/hydrophobic and electrostatic interactions play critical roles for the binding. The binding mode of PIK75 for PI3Kα is predicted. The conserved hydrophobic adenine region of PI3Kα made up of Ile800, Ile848, Val850, Val851, Met922, Phe930, and Ile932 accommodates the flat 6-bromine imidazo[1,2-a]pyridine ring of PIK75. The 2-methyl-5-nitrophenyl group of PIK75 extends to the P-loop region, and has four hydrogen-bond arms with the backbone and side chain of Ser773 and Ser774. And the distinct conformation of the P-loop induced by PIK75 is speculated to be responsible for the selectivity profile of PIK75. The predicted binding mode of PIK75 for PI3Kα presented in this study may help design high affinity and selective compounds to target PI3Kα.