Sodium citrate-assisted synthesis of nano-manganese oxide on carbon fiber for enhancing the mechanical and frictional performances of carbon fiber-reinforced resin matrix composites

Aiming to enhance the carbon fiber (CF)/resin interfacial adhesion, this report describes the novel application of sodium citrate (SC) as an auxiliary reducing agent and surface regulator to control the morphology of nano-manganese dioxide (MnO₂) on the CF surface. The composites were fabricated by means of controlling the molar concentration ratio of SC to Mn source (0:1, 1:3, 1:2, and 1:1) in hydrothermal synthesis. The results reveal that MnO₂ nanosheets on the CF surface become denser as the concentration of SC is 1/3 of Mn source, which makes advance to the surface roughness and surface energy of CF. Simultaneously, the tensile strength of as-prepared composite is increased by 52.8%. The homologous friction coefficient tends to be high and stable and the wear volume is significantly reduced by 63.8 and 26.5% under the applied loads of 3 and 5 N in contrast with the original composites prepared without SC. As a result, it can be inferred that SC plays a crucial role in enhancing the interfacial bonding strength between the CF and matrix, providing insights into the interface control of CF-reinforced resin matrix composites.     

Improvements of the structural,thermal, and mechanical properties of structural adhesive with functionalized boron nitride nanoparticles

Investigations on the production and development of nanoparticle-reinforced polymer materials have been attracted attention by researchers. Various nanoparticles have been used to improve the mechanical, chemical, thermal, and physical properties of polymer matrix composites. Boron compounds come to the fore to improve the mechanical and thermal properties of polymers. In this study, mechanical, thermal, and structural properties of structural adhesive have been examined by adding nano hexagonal boron nitride (h-BN) to epoxy matrix at different percentages (0.5, 1, 2, 3, 4, and 5%). For this purpose, nano h-BN particles were functionalized with 3-aminopropyltriethoxysilane (APTES) to disperse the h-BN nanoparticles homogeneously in epoxy matrix and to form a strong bond at the matrix interface. Two-component structural epoxy adhesive was modified by using functionalized h-BN nanoparticles. The structural and thermal properties of the modified adhesives were investigated by scanning electron microscopy and energy dispersion X-ray spectroscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry, and thermogravimetric analysis techniques. Tensile test and dynamic mechanical analysis were performed to determine the mechanical properties of the adhesives. When the results obtained from analysis were examined, it was seen that the nano h-BN particles functionalized with APTES were homogeneously dispersed in the epoxy matrix and formed a strong bond. In addition that, it was concluded from the experimental results that the thermal and mechanical properties of adhesives were improved by adding functionalized nano h-BN particles into epoxy at different ratios.     

Synthesis and evaluating of carbon nanoallotrope-biomacromolecule gel composites as drug delivery systems

This work was done to assess the role of precursors (agro and graphite) on performance of carbon nanoallotropes-biomacromolecules composite as drug delivery for controlling the release of niacin. In this respect graphene oxide and bagasse-based carbon oxide were synthesized and chelated with chitosan (Cs-GO and Cs-Co). These gel composites were characterized by many techniques [morphology, differential scanning calorimetry, Fourier-transform infrared spectroscopy, swelling, encapsulation efficiency (EE) and loading (L) % of niacin. Another series of experiments was carried out for studying the role of replacing part of carbon nanoallotrope by carboxymethyl cellulose (CMC) on performance of produced drug carries, these systems were coded as Cs-GO-CMC and Cs-Co-CMC. The data showed that, the Cs-GO gel composite provided maximum release of NA, at 5 h, for pH's simulated gastric and intestinal fluids; pH. 2.1 and pH 7.4 (1120 mg/L and 757 mg/L). The incorporation of CMC is not acceptable as it provided low drug release together with burst release of NA-drug, and consequently possible caused tissue irritation or toxicity in the human body. The Cs-GO and Cs-CO systems with relatively low drug loading were recommended for their better controllability system to NA release, which prolonging benefit of human with niacin. The NA release from all investigated gels followed Fickian and non-Fickian diffusion mechanisms.     

Effect of modified layered double hydroxide on the flammability of intumescent flame retardant PP nanocomposites

The dodecyl sulfate intercalated CaMgAl-hydrotalcites (layered double hydroxides [LDHs]) were successfully prepared by co-precipitation method, and characterized by X-ray diffraction analysis, infrared spectroscopy (Fourier transform infrared spectra [FT-IR]), thermogravimetry (TG-DTA), scanning electron microscope, and Brunner−Emmet−Teller (BET). The prepared LDHs were added to the intumescent flame retardant (IFR) polypropylene (PP) nanocomposites, and the limiting oxygen index method (LOI), vertical combustion method (UL-94), cone calorimetry (CCT), and other test methods were used to study its thermal stability and combustion performance. The results showed that when the flame retardant was composed of 23 wt% IFR and 2 wt% O-SDS-LDHs, the LOI value of the material was increased to 31.5%, reaching the V-0 level, and the flame retardant performance was significantly improved. The results also showed that there was a significant synergistic effect between IFR and O-SDS-LDHs, which could improve the thermal stability and graphitization degree of PP nanocomposites. In addition, the peak heat release rate, total heat release, and total smoke production of the PP/IFR/O-SDS-LDHs system were 177 kW/m², 101 MJ/m², and 15.4 m², respectively, which were 82.2%, 51.0%, and 23.0% lower than those of pure PP, respectively. These improvements could be attributed to the presence of dense and continuous char layer formed by the synergistic effect.     

Influence of deposited amine-functionalized Si-MCM-41 in polyacrylonitrile electrospun membranes applied for separation of water in oil emulsions

Among several oil/water emulsion separation technologies, the utilization of nanoparticle-decorated membranes with diverse functionalities has received considerable attention in recent years, particularly if the antifouling capacity can be improved. In this article, we propose a new membrane based on surface-hydrolyzed polyacrylonitrile electrospun membranes and/or decorated with amine-functionalized Si-MCM-41 nanoparticles to be used as oil/water emulsion separation treatment and to determine their antifouling ability. X-Ray photoelectron spectrometry, attenuated total reflectance Fourier transform infrared spectroscopy, and toluidine blue O assay, scanning electron microscopy, contact angle measurements for oil under water and thermogravimetry were used for characterizing the membranes and an assay of permeability was developed to quantify the diffusion of oil molecules across the electrospun membrane. The electrospun and/or decorated membranes showed an underwater oleophobic wettability, which can separate oil-in-water emulsions with 87% separation efficiency, results of fouling experiments, evaluated in terms of rejection and flux recovery ratio, exhibited good antifouling ability, but the membrane decoration process did not lead to superior outcomes compared with undecorated membranes.     

微/纳米氧化钨晶须的制备工艺及原理

采用溶胶-水热反应法，通过添加适量的硫化钠结晶体诱导制备了微／纳米氧化钨晶须。利用扫描电镜观察氧化钨样品的形貌特征，并对氧化钨晶须进行能谱测试，用X射线衍射仪对氧化钨样品进行物相分析和晶面测定，用透射电镜观察微／纳米氧化钨晶须／线的生长特征。结果表明：未添加硫酸钠时，在180℃水热反应12～36h只能得到氧化钨颗粒粉末，而添加适量硫化钠后，可制备出直径为0．2～0．3μm、长径比为5～50的氧化钨晶须和直径为10～30nm、长径比为50～200的氧化钨纳米线；氧化钨纳米线晶体结构良好，物相为六方晶系WO3；微／纳米氧化钨晶须／线主要沿〈200〉，〈002〉，〈202〉和〈100〉方向定向生长。     

SrTiO3微纳米线的制备与亲疏水性

采用水热法，使用层状钛酸盐纳米线和氢氧化锶作为前驱物，在一定反应温度和反应时间的条件下简单地制备出了超细SrTiO3粉体。结果表明，只有在反应条件和反应物配比合适时才能得到纯的SrTiO3粉体。用X-射线粉末衍射仪和扫描电镜对SrTiO3粉体进行了表征。结果表明，所制备的SrTiO3粉体绝大部分为线状，长度约20μm，直径100～500nm。用接触角仪对所制备的SrTiO3粉体的亲疏水性进行了研究。结果表明，随着反应时间的延长，反应产物SrTiO3的纯度逐渐增加，由原来的完全亲水性转变为疏水性，接触角为36．820。     

Breaking the Responsivity-Bandwidth Trade-Off Limit in GaN Photoelectrodes for High-Response and Fast-Speed Optical Communication Application

Underwater optical communication (UOC) has attracted considerable interest in the continuous expansion of human activities in marine/ocean environments. The water-durable and self-powered photoelectrodes that act as a battery-free light receiver in UOC are particularly crucial, as they may directly face complex underwater conditions. Emerging photoelectrochemical (PEC)-type photodetectors are appealing owing to their intrinsic aqueous operation characteristics with versatile tunability of photoresponses. Herein, a self-powered PEC photodetector employing n-type gallium nitride (GaN) nanowires as a photoelectrode, which is decorated with an iridium oxide (IrO_x) layer to optimize charge transfer dynamics at the GaN/electrolyte interface, is reported. Strikingly, the constructed n-GaN/IrO_x photoelectrode breaks the responsivity-bandwidth trade-off limit by simultaneously improving the response speed and responsivity, delivering an ultrafast response speed with response/recovery times of only 2 µs/4 µs while achieving a high responsivity of 110.1 mA W⁻¹. Importantly, the device exhibits a large bandwidth with 3 dB cutoff frequency exceeding 100 kHz in UOC tests, which is one of the highest values among self-powered photodetectors employed in optical communication system.     

A Sensing and Stretchable Polymer-Dispersed Liquid Crystal Device Based on Spiderweb-Inspired Silver Nanowires-Micromesh Transparent Electrode

Polymer-dispersed liquid crystal (PDLC) devices are truly promising optical modulators for information display, smart window as well as intelligent photoelectronic applications due to their fast switching, large optical modulation as well as cost-effectiveness. However, realizing highly soft PDLC devices with sensing function remains a grand challenge because of the intrinsic brittleness of traditional transparent conductive electrodes. Here, inspired by spiderweb configuration, a novel type of silver nanowires (AgNWs) micromesh-based stretchable transparent conductive electrodes (STCEs) is developed to support the realization of soft PDLC device. Benefiting from the embedding design of AgNWs micromesh in polydimethylsiloxane (PDMS), the STCEs can maintain excellent electrical conductivity and transparency even in various extreme conditions such as bending, folding, twisting, stretching as well as multiple chemical corrosion. Further, STCEs with the embedded AgNWs micromesh endow the assembled PDLC device with excellent photoelectrical properties including rapid switching speed (<1 s), large optical modulation (69% at 600 nm), as well as robust mechanical stability (bending over 1000 cycles and stretching to 40%). Moreover, the device displays the pressure sensing function with high sensitivity in response to pressure stimulus. It is conceivable that AgNWs micromesh transparent electrodes will shape the next generation of related soft smart electronics.     

Tungsten wires and porous NiAl prepared through directional solidification and selective dissolution

The combination of directional solidification and selective dissolution was applied to fabricate tungsten (W) wires and porous NiAl matrix. A NiAl–W pseudobinary eutectic alloy with 1.5?at.% tungsten was directionally solidified in a Bridgman-type oven at 1700°C. Results confirmed that the relationships of the growth rate with the interfibrous spacing and diameter of W fibrous phases in the directionally solidified samples are in accordance with the Jackson and Hunt (J?H) model. Afterward, the NiAl matrix was selectively dissolved in an HCl:H₂O₂ solution to reveal W wires, which present various three-dimensional (3D) morphologies at different growth rates. The W fibrous phases in the NiAl–W alloy samples were then selectively removed with a mixed etchant of ammonium acetate to form a porous NiAl matrix at a constant potential. Dynamic corrosion curves revealed that etching W from the NiAl matrix was inhibited after 2–3?h. The porous structures of NiAl after removing W phases are linked to the 3D morphologies of W fibrous phases embedded in the NiAl matrix. The aspect ratio of W wires and the structures of porous NiAl can be adjusted by selecting the process parameters of this combined technology.