Optimization of anti-wear and anti-bacterial properties of beta TiNb alloy via controlling duty cycle in open-air laser nitriding

A multifunctional beta TiNb surface, featuring wear-resistant and antibacterial properties, was successfully created by means of open-air fibre laser nitriding. Beta TiNb alloy was selected in this study as it has low Young’s modulus, is highly biocompatible, and thus can be a promising prosthetic joint material. It is, however, necessary to overcome intrinsically weak mechanical properties and poor wear resistance of beta TiNb in order to cover the range of applications to loadbearing and/or shearing parts. To this end, open-air laser nitriding technique was employed. A control of single processing parameter, namely duty cycle (between 5% and 100%), led to substantially different structural and functional properties of the processed beta TiNb surfaces as analyzed by an array of analytical tools. The TiNb samples nitrided at the DC condition of 60% showed a most enhanced performance in terms of improving surface hardness, anti-friction, antiwear and anti-bacterial properties in comparison with other conditions. These findings are expected to be highly important and useful when TiNb alloys are considered as materials for hip/knee articular joint implant

The Response of Lateral Flow to Peak River Discharge in a Macrotidal Estuary

The Ou River, a medium-sized river in southeastern China, is selected to study the lateral flow response to rapidly varied river discharge, i.e., peak river discharge (PRD). A three-dimensional model based on the Finite-Volume Community Ocean Model is validated by in situ measurements from 15 June to 16 July 2005. PRD, which considers the extra buoyancy and longitudinal momentum in a short time, rebuilds the stratification and lateral flow. PRD, compared with low-discharge, generally makes stratification stronger and lateral flow weaker. PRD mainly rebuilds lateral flow by changing lateral advection, lateral Coriolis, and lateral-barotropic pressure gradient terms. After PRD, the salinity recovery time is longer than that of the flow because the impact on buoyancy lasts longer than that on longitudinal flow. Longitudinal flow is mostly affected by the momentum transferred during PRD; therefore, the recovery time is close to the flooding duration. However, the lateral flow is affected by the buoyancy, and its recovery time is generally longer than the flooding duration. The lateral flow recovery time depends on transect width, flow velocity and the variation caused by PRD. PRD occurs widely in global small-/medium-sized river estuaries, and the result of this work can be extended to other estuaries

The Response of Turbidity Maximum to Peak River Discharge in a Macrotidal Estuary

The Ou River, a medium-sized river in the southeastern China, is examined to study the estuarine turbidity maximum (ETM) response to rapidly varied river discharge, i.e., peak river discharge (PRD). This study analyzes the difference in ETM and sediment transport mechanisms between low-discharge and PRD during neap and spring tides by using the Finite-Volume Community Ocean Model. The three-dimensional model is validated by in-situ measurements from 23 April to 22 May 2007. In the Ou River Estuary (ORE), ETM is generally induced by the convergence between river runoff and density-driven flow. The position of ETM for neap and spring tides is similar, but the suspended sediment concentration during spring tide is stronger than that during neap tide. The sediment source of ETM is mainly derived from the resuspension of the seabed. PRD, compared with low-discharge, can dilute the ETM, but cause more sediment to be resuspended from the seabed. The ETM is more seaward during PRD. After PRD, the larger the peak discharge, the longer the recovery time will be. Moreover, the river sediment supply helps shorten ETM recovery time. Mechanisms for this ETM during a PRD can contribute to studies of morphological evolution and pollutant flushing

The hybridization of Ag2CO3 rods with g-C3N4 sheets with improved photocatalytic activity

A series of graphitic carbon nitride/silver carbonate (g-C3N4/Ag2CO3) rod-like composites with different weight contents of g-C3N4 have been prepared by a facile precipitation method. The g-C3N4/Ag2CO3 rod-like composites exhibited higher photocatalytic activity than pure Ag2CO3 toward degradation of rhodamine B (RhB) and methylene blue (MB) under visible-light irradiation. The photocatalytic reaction follows a pseudo-first-order reaction and the rate constants for the degradation of RhB and MB by 3.5% g-C3N4/Ag2CO3 are about 2 times and 1.7 times that of pure Ag2CO3, respectively. A possible photocatalytic mechanism was proposed based on the photoluminescence (PL) spectra and a series of radical trapping experimental analyses. The remarkably improved photocatalytic performance should be ascribed to the heterostructure between Ag2CO3 and g-C3N4, which greatly promoted the photoinduced charge transfer and inhibited the recombination of electrons and holes

One-Step Construction of Tryptophan-Derived Small Molecule Hydrogels for Antibacterial Materials

Amino acid-based hydrogels have received widespread attention because of their wide range of sources, biodegradability, and biocompatibility. Despite considerable progress, the development of such hydrogels has been limited by critical problems such as bacterial infection and complex preparation. Herein, by using the non-toxic gluconolactone (GDL) to adjust the pH of the solution to induce the rapid self-assembly of N-[(benzyloxy)carbonyl]-L-tryptophan (ZW) to form a three-dimensional (3D) gel network, we developed a stable and effective self-assembled small-molecule hydrogel. Characterization assays and molecular dynamics studies indicate that π–π stacking and hydrogen bonding are the main drivers of self-assembly between ZW molecules. In vitro experiments further confirmed this material’s sustained release properties, low cytotoxicity, and excellent antibacterial activity, particularly against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus. This study provides a different and innovative perspective for the further development of antibacterial materials based on amino acid derivatives

Effect of Polymer Addition on the Structure and Hydrogen Evolution Reaction Property of Nanoflower-Like Molybdenum Disulfide

Nano-structured molybdenum disulfide (MoS2) catalysts have been extensively developed for the hydrogen evolution reaction (HER). Herein, a novel hydrothermal intercalation approach is employed to fabricate nanoflower-like 2H–MoS2 with the incorporation of three polymers, polyvinylpyrrolidone (PVP), polyvinyl alcohol (PVA), and polyethylenimine (PEI). The as-prepared MoS2 specimens were characterized by techniques of scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), together with Raman and Fourier transform infrared spectroscopy (FTIR). The HER properties of these lamellar nanoflower-like composites were evaluated using electrochemical tests of linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). The existent polymer enlarges the interlayer spacing of the lamellar MoS2, and reduces its stacked thickness. The lamellar MoS2 samples exhibit a promoting activity in HER at low additions of these three polymers (0.04 g/g MoS2 for PVA and PEI, and 0.08 g/g MoS2 for PVP). This can be attributed to the fact that the expanded interlayer of MoS2 can offer abundant exposed active sites for HER. Conversely, high additions of the polymers exert an obvious interference in the HER activity of the lamellar MoS2. Compared with the samples of MoS2/PVP–0.08 and MoS2/PEI–0.04, the MoS2/PVA–0.04 composite exhibits excellent activity in HER, in terms of higher current density and lower onset potential

An Intelligent Multi-Sensor Variable Spray System with Chaotic Optimization and Adaptive Fuzzy Control

During the variable spray process, the micro-flow control is often held back by such problems as low initial sensitivity, large inertia, large hysteresis, nonlinearity as well as the inevitable difficulties in controlling the size of the variable spray droplets. In this paper, a novel intelligent double closed-loop control with chaotic optimization and adaptive fuzzy logic is developed for a multi-sensor based variable spray system, where a Bang-Bang relay controller is used to speed up the system operation, and adaptive fuzzy nonlinear PID is employed to improve the accuracy and stability of the system. With the chaotic optimization of controller parameters, the system is globally optimized in the whole solution space. By applying the proposed double closed-loop control, the variable pressure control system includes the pressure system as the inner closed-loop and the spray volume system as the outer closed-loop. Thus, the maximum amount of spray droplets deposited on the plant surface may be achieved with the minimum medicine usage for plants. Multiple sensors (for example: three pressure sensors and two flow rate sensors) are employed to measure the system states. Simulation results show that the chaotic optimized controller has a rise time of 0.9 s, along with an adjustment time of 1.5 s and a maximum overshoot of 2.67% (in comparison using PID, the rise time is 2.2 s, the adjustment time is 5 s, and the maximum overshoot is 6.0%). The optimized controller parameters are programmed into the hardware to control the established variable spray system. The experimental results show that the optimal spray pressure of the spray system is approximately 0.3 MPa, and the flow rate is approximately 0.08 m3/h. The effective droplet rate is 89.4%, in comparison to 81.3% using the conventional PID control. The proposed chaotically optimized composite controller significantly improved the dynamic performance of the control system, and satisfactory control results are achieved

Molecular Dynamics-Assisted Design of High Temperature-Resistant Polyacrylamide/Poloxamer Interpenetrating Network Hydrogels

Polyacrylamide has promising applications in a wide variety of fields. However, conventional polyacrylamide is prone to hydrolysis and thermal degradation under high temperature conditions, resulting in a decrease in solution viscosity with increasing temperature, which limits its practical effect. Herein, combining molecular dynamics and practical experiments, we explored a facile and fast mixing strategy to enhance the thermal stability of polyacrylamide by adding common poloxamers to form the interpenetrating network hydrogel. The blending model of three synthetic polyacrylamides (cationic, anionic, and nonionic) and poloxamers was first established, and then the interaction process between them was simulated by all-atom molecular dynamics. In the results, it was found that the hydrogen bonding between the amide groups on all polymers and the oxygen-containing groups (ether and hydroxyl groups) on poloxamers is very strong, which may be the key to improve the high temperature resistance of the hydrogel. Subsequent rheological tests also showed that poloxamers can indeed significantly improve the stability and viscosity of nonionic polyacrylamide containing only amide groups at high temperatures and can maintain a high viscosity of 3550 mPa·S at 80 °C. Transmission electron microscopy further showed that the nonionic polyacrylamide/poloxamer mixture further formed an interpenetrating network structure. In addition, the Fourier transform infrared test also proved the existence of strong hydrogen bonding between the two polymers. This work provides a useful idea for improving the properties of polyacrylamide, especially for the design of high temperature materials for physical blending