Preparation of TiO 2

Photocatalysts comprising nanosized TiO2 particles on activated carbon (AC) were prepared by a sol-gel method. The TiO2/AC composites were characterized by X-ray diffraction (XRD), thermogravimetric (TG) analysis, nitrogen adsorption, scanning electron microscope (SEM), transmission electron microscope (TEM), and energy dispersive X-ray (EDX). Their photocatalytic activities were studied through the degradation of Rhodamine B (RhB) in photocatalytic reactor at room temperature under ultraviolet (UV) light irradiation and the effect of loading cycles of TiO2 on the structural properties and photocatalytic activity of TiO2/AC composites was also investigated. The results indicate that the anatase TiO2 particles with a crystal size of 10–20 nm can be deposited homogeneously on the AC surface under calcination at 500°C. The loading cycle plays an important role in controlling the loading amount of TiO2 and morphological structure and photocatalytic activity of TiO2/AC composites. The porosity parameters of these composite photocatalysts such as specific surface area and total pore volume decrease whereas the loading amount of TiO2 increases. The TiO2/AC composite synthesized at 2 loading cycles exhibits a high photocatalytic activity in terms of the loading amount of TiO2 and as high as 93.2% removal rate for RhB from the 400 mL solution at initial concentration of 2 × 10−5 mol/L under UV light irradiation

Oxygen Reduction Activity and Stability of Composite Pdx/Co-Nanofilms/C Electrocatalysts in Acid and Alkaline Media

The morphology tuning of Pd and Pd-M nanoparticles is one of the significant strategies to control the catalytic activity toward oxygen reduction reaction (ORR). In this study, composite Pdx/Co-nanofilms/C electrocatalysts of Pd nanoparticles implanted onto Co nanofilms were synthesized on an immiscible ionic liquid (IL)/water interface for ORR. The Pd nanoparticles implanted onto Co nanofilms show a marked distortion of crystal lattice and surface roughness. These Pdx/Co-nanofilms/C electrocatalysts exhibit enhanced activity for ORR compared with Pd/C and PdxCo/C catalysts in both acid and alkaline solutions, in which the Pd3/Co-nanofilms/C catalyst displays the highest ORR mass activity. The superior ORR mass activities of the fabricated Pdx/Co-nanofilms/C catalysts may be mainly attributed to their larger catalytic areas, which are conferred by the rough surface of Pd nanoparticles with a distorted crystal lattice, and the synergistic effect between the surface Pd atoms and the 2D Co nanofilm substrate. The relationship between ORR mass activity and Pd/Co atom ratio varies in different electrolytes. Furthermore, by using proper heat-treatment methods, the Pdx/Co-nanofilms/C catalysts exhibit improved cycling stability compared with pure Pd/C catalyst after extended potential cycling

Biomimetic Prosthetic Hand Enabled by Liquid Crystal Elastomer Tendons.

As one of the most important prosthetic implants for amputees, current commercially available prosthetic hands are still too bulky, heavy, expensive, complex and inefficient. Here, we present a study that utilizes the artificial tendon to drive the motion of fingers in a biomimetic prosthetic hand. The artificial tendon is realized by combining liquid crystal elastomer (LCE) and liquid metal (LM) heating element. A joule heating-induced temperature increase in the LCE tendon leads to linear contraction, which drives the fingers of the biomimetic prosthetic hand to bend in a way similar to the human hand. The responses of the LCE tendon to joule heating, including temperature increase, contraction strain and contraction stress, are characterized. The strategies of achieving a constant contraction stress in an LCE tendon and accelerating the cooling for faster actuation are also explored. This biomimetic prosthetic hand is demonstrated to be able to perform complex tasks including making different hand gestures, holding objects of different sizes and shapes, and carrying weights. The results can find applications in not only prosthetics, but also robots and soft machines. &nbsp;</p

Stretchable, Rehealable, Recyclable, and Reconfigurable Integrated Strain Sensor for Joint Motion and Respiration Monitoring

Cutting-edge technologies of stretchable, skin-mountable, and wearable electronics have attracted tremendous attention recentlydue to their very wide applications and promising performances. One direction of particular interest is to investigate novel properties in stretchable electronics by exploring multifunctional materials. Here, we report an integrated strain sensing system that is highly stretchable, rehealable, fully recyclable, and reconfigurable. This system consists of dynamic covalent thermoset polyimine as the moldable substrate and encapsulation, eutectic liquid metal alloy as the strain sensing unit and interconnects, and off-the-shelf chip components for measuring and magnifying functions. The device can be attached on different parts of the human body for accurately monitoring joint motion and respiration. Such a strain sensing system provides a reliable, economical, and ecofriendly solution to wearable technologies, with wide applications in health care, prosthetics, robotics, and biomedical devices.</p

Investigating the self-healing of dynamic covalent thermoset polyimine and its nanocomposites

Self-healable and recyclable materials and electronics can improve the reliability and repairability, and can reduce environmental pollution, therefore they promise very broad applications. In this study, we investigated the self-healing performance of dynamic covalent thermoset polyimine and its nanocomposites based on dynamic covalent chemistry. Heat press was applied to two laminating films of polyimine and its nanocomposites to induce self-healing. The effects of heat press time, temperature and load on the interfacial shear strength of re-healed films were investigated. The results showed that increasing the heat press time, temperature and load can significantly improve the interfacial shear strength and thus the self-healing effect. For polyimine nanocomposites, increasing the heat press time, temperature and load led to improved electrical conductivity of the re-healed films.</p

Improved Design of Highly Efficient Microsized Lithium-Ion Batteries for Stretchable Electronics

We introduce a stretchable microsized Li-ion battery with a novel design. The battery was fabricated using a facile technique and exhibited high performance. Dry-etching process was utilized to pattern lithium phosphorus oxynitride for avoiding the use of a photoresist developer (photolithography), which can damage the amorphous lithium manganese oxide (LiMn2O4 (LMO)) cathode. This allowed us to fabricate the current collectors and electrodes away from the main body of the microsized battery (a parallel structure rather than a stacked, i.e. perpendicular structure). An enhanced capacity of ~150 mAh g&minus;1 was achieved using the parallel device structure at a charge&ndash;discharge average potential of 3.7 V; in comparison, the performance of a device with a stacked structure was significantly inferior. The microsized batteries were utilized to illuminate a white inorganic light-emitting diode with a turn-on voltage of ~2.5 V. The fabricated devices with the stacked structure were transferred to a mechanically prestrained (~22.5%) polydimethylsiloxane polymer via a kinetic transfer process. Upon removal of the prestrain, the shrinkage of the substrate caused buckle formation at the interconnects, and tensile damage to the microsized batteries was circumvented. The simulation (COMSOL) results indicated that most of the strain in the standby form (without applied stretching) was concentrated at the interconnects, preventing significant damage in the main device area. Upon the application of 21% stretching (load), although the parallel structure exhibits slightly higher maximum strain in the islands, the strain distribution was more effectively managed, indicating the potential of the proposed method for various stretchable and bendable optoelectronic applications. </div

Rubber Toughened and Nanoparticle Reinforced Epoxy Composites

Epoxy resins have achieved acceptance as adhesives, coatings, and potting compounds, but their main application is as matrix to produce reinforced composites. However, their usefulness in this field still limited due to their brittle nature. Some studies have been done to increase the toughness of epoxy composites, of which the most successful one is the modification of the polymer matrix with a second toughening phase. Resin Transfer Molding (RTM) is one of the most important technologies to manufacture fiber reinforced composites. In the last decade it has experimented new impulse, due to its favorable application to produce large surface composites with good technical properties and at relative low cost. This research work focuses on the development of novel modified epoxy matrices, with enhanced mechanical and thermal properties, suitable to be processed by resin transfer molding technology, to manufacture Glass Fiber Reinforced Composites (GFRC’s) with improved performance in comparison to the commercially available ones. In the first stage of the project, a neat epoxy resin (EP) was modified using two different nano-sized ceramics: silicium dioxide (SiO2) and zirconium dioxide (ZrO2); and micro-sized particles of silicone rubber (SR) as second filler. Series of nanocomposites and hybrid modified epoxy resins were obtained by systematic variation of filler contents. The rheology and curing process of the modified epoxy resins were determined in order to define their aptness to be processed by RTM. The resulting matrices were extensively characterized qualitatively and quantitatively to precise the effect of each filler on the polymer properties. It was shown that the nanoparticles confer better mechanical properties to the epoxy resin, including modulus and toughness. It was possible to improve simultaneously the tensile modulus and toughness of the epoxy matrix in more than 30 % and 50 % respectively, only by using 8 vol.-% nano-SiO2 as filler. A similar performance was obtained by nanocomposites containing zirconia. The epoxy matrix modified with 8 vol.-% ZrO2 recorded tensile modulus and toughness improved up to 36% and 45% respectively regarding EP. On the other hand, the addition of silicone rubber to EP and nanocomposites results in a superior toughness but has a slightly negative effect on modulus and strength. The addition of 3 vol.-% SR to the neat epoxy and nanocomposites increases their toughness between 1.5 and 2.5 fold; but implies also a reduction in their tensile modulus and strength in range 5-10%. Therefore, when the right proportion of nanoceramic and rubber were added to the epoxy resin, hybrid epoxy matrices with fracture toughness 3 fold higher than EP but also with up to 20% improved modulus were obtained. Widespread investigations were carried out to define the structural mechanisms responsible for these improvements. It was stated, that each type of filler induces specific energy dissipating mechanisms during the mechanical loading and fracture processes, which are closely related to their nature, morphology and of course to their bonding with the epoxy matrix. When both nanoceramic and silicone rubber are involved in the epoxy formulation, a superposition of their corresponding energy release mechanisms is generated, which provides the matrix with an unusual properties balance. From the modified matrices glass fiber reinforced RTM-plates were produced. The structure of the obtained composites was microscopically analyzed to determine their impregnation quality. In all cases composites with no structural defects (i.e. voids, delaminations) and good superficial finish were reached. The composites were also properly characterized. As expected the final performance of the GFRCs is strongly determined by the matrix properties. Thus, the enhancement reached by epoxy matrices is translated into better GFRC´s macroscopical properties. Composites with up to 15% enhanced strength and toughness improved up to 50%, were obtained from the modified epoxy matrices

Epidemiology and clinical course of COVID-19 in Shanghai, China.

Background: Novel coronavirus pneumonia (COVID-19) is prevalent around the world. We aimed to describe epidemiological features and clinical course in Shanghai. Methods: We retrospectively analysed 325 cases admitted at Shanghai Public Health Clinical Center, between January 20 and February 29, 2020. Results: 47.4% (154/325) had visited Wuhan within 2 weeks of illness onset. 57.2% occurred in 67 clusters; 40% were situated within 53 family clusters. 83.7% developed fever during the disease course. Median times from onset to first medical care, hospitalization and negative detection of nucleic acid by nasopharyngeal swab were 1, 4 and 8 days. Patients with mild disease using glucocorticoid tended to have longer viral shedding in blood and feces. At admission, 69.8% presented with lymphopenia and 38.8% had elevated D-dimers. Pneumonia was identified in 97.5% (314/322) of cases by chest CT scan. Severe-critical patients were 8% with a median time from onset to critical disease of 10.5 days. Half required oxygen therapy and 7.1% high-flow nasal oxygen. The case fatality rate was 0.92% with median time from onset to death of 16 days. Conclusion: COVID-19 cases in Shanghai were imported. Rapid identification, and effective control measures helped to contain the outbreak and prevent community transmission