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NiTi shape memory alloys (SMAs) are inevitably in contact with hydrogen in specific service environments, which can degrade their mechanical behaviors. In this work, the effect of hydrogen on the super-elasticity of NiTi SMA orthodontic wires is investigated experimentally and theoretically. Firstly, cathodic hydrogen charging was performed for the wires at a current density of 10A/m with various charging times (2.5min, 5min, 7.5min and 10min) and charging lengths (20 mm, 40 mm, 60 mm and 80 mm) in 0.5 mol/L H2SO4+2 g/L CH4N2S electrolyte solution at room temperature. Then, ex-situ tension-unloading tests were carried out shortly after the hydrogen charging. The stress-strain responses showed a two-step martensite transformation (MT), i.e., the start stress of MT for the region with hydrogen charging is much larger than that without hydrogen charging. Based on the experimental observations, a diffusional-mechanically coupled constitutive model is constructed. Elastic strain, transformation strain, transformation-induced plasticity (TRIP) and hydrogen swelling deformation are considered. The effect of hydrogen on the thermo-mechanical behavior of NiTi SMA is taken into account by introducing the hydrogen concentration (HC)-dependent critical temperatures of MT and slip resistance of TRIP. The thermodynamic driving forces of MT and TRIP are derived from the constructed Helmholtz free energy and dissipation inequality. The balance equation of hydrogen diffusion is obtained by the chemical potential and Fick's diffusion law. To obtain the overall response of the wire with a heterogeneous HC field, a scale transition rule is proposed. The capability of the proposed model to describe the super-elasticity of NiTi SMA with various hydrogen charging times and charging lengths is validated by comparing the predicted results with the experimental ones.
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http://dx.doi.org/10.1016/j.jmbbm.2022.105276 | DOI Listing |
Environ Sci Pollut Res Int
September 2025
Department of Dyes and Chemical Engineering, Bangladesh University of Textiles, Dhaka, Bangladesh.
This study quantitatively evaluated the adsorption performance of natural bentonite for removing three dye classes-cationic (Basic dye: BEZACRYL RED GRL), anionic (Reactive dye: AVITERA LIGHT RED SE), and non-ionic (Disperse dye: BEMACRON BLUE HP3R) from synthetic textile wastewater. Batch adsorption experiments were conducted under varying conditions of contact time (15-90 min), adsorbent dosage (20-60 g L⁻), pH (4 and 12), and temperature (25-100 °C), with dye concentrations quantified by UV-Vis spectroscopy. At a contact time of 30 min and room temperature (25 °C), maximum removal efficiencies reached 99.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Center for Innovative Materials and Architectures, Ho Chi Minh City 700000, Viet Nam; Vietnam National University, Ho Chi Minh City 700000, Viet Nam. Electronic address:
Organic nucleophile-assisted natural seawater electrolysis has emerged as a promising strategy for green hydrogen production by significantly reducing energy consumption. Among Ni-based electrocatalysts, NiMoO has drawn attention for its activity in both oxygen evolution reaction (OER) and urea oxidation reaction (UOR). However, its practical application is hindered by severe surface passivation, particularly at industrial current densities (e.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Thermal Science and Energy Engineering, University of Science and Technology of China, 96 Jinzhai Road, Hefei 230026, PR China. Electronic address:
Heterojunctions have garnered significant attention in the field of photocatalysis due to their exceptional ability to facilitate the separation of photogenerated charge carriers and their high efficiency in hydrogen reaction. However, their overall photocatalytic performance is often constrained by electron transport rates and suboptimal hydrogen adsorption/desorption kinetics. To address these challenges, this study develops a g-CN/MoS@MoC dual-effect synergistic solid-state Z-type heterojunction, synthesized through the in-situ sulfurization of MoC combined with ultrasonic self-assembly technique.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, PR China. Electronic address:
Transition metal fluorides because of the high electronegativity of fluorine may enhance the local electron density of the metal sites and promote water molecule dissociation and charge transfer. However, enhancing the intrinsic activity of fluorides to improve material stability remains a challenge. Herein, we develop an innovative four-step synthetic strategy (electrochemical deposition → co-precipitation → ligand exchange → in situ fluorination) to engineer three-dimensional porous Fe-doped CoF nanocubes vertically anchored on MXene (Fe-CoF/MXene/NF).
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266580, China.
Reaction intermediates (RI) are key factors that directly determine the efficiency of the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). In this study, a local electric field microenvironment was built in a FeNi and MoNi heterostructure (H-FeNiMo/NMF) to induce the redistribution of hydroxyls and protons on the metal sites during the OER and HER. H-FeNiMo/NMF requires only 270 and 155 mV to reach 100 mA cm in alkaline media for OER and HER, respectively.
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