Reduction In Resistance Research Articles

Bioengineering the Human Intestinal Mucosa and the Importance of Stromal Support for Pharmacological Evaluation In Vitro

Drug discovery is associated with high levels of compound elimination in all stages of development. The current practices for the pharmacokinetic testing of intestinal absorption combine Transwell® inserts with the Caco-2 cell line and are associated with a wide range of limitations. The improvement of pharmacokinetic research relies on the development of more advanced in vitro intestinal constructs that better represent human native tissue and its response to drugs, providing greater predictive accuracy. Here, we present a humanized, bioengineered intestinal construct that recapitulates aspects of intestinal microanatomy. We present improved histotypic characteristics reminiscent of the human intestine, such as a reduction in transepithelial electrical resistance (TEER) and the formation of a robust basement membrane, which are contributed to in-part by a strong stromal foundation. We explore the link between stromal–epithelial crosstalk, paracrine communication, and the role of the keratinocyte growth factor (KGF) as a soluble mediator, underpinning the tissue-specific role of fibroblast subpopulations. Permeability studies adapted to a 96-well format allow for high throughput screening and demonstrate the role of the stromal compartment and tissue architecture on permeability and functionality, which is thought to be one of many factors responsible for unexpected drug outcomes using current approaches for pharmacokinetic testing.

Enhanced plasmonic performance of TiO2 derived TiN films via gas nitridation

This study demonstrates a cost-effective method for planar titanium nitride plasmonic film by nitriding spin-coated TiO2 in ammonia atmosphere. The effect of nitridation temperature on the structural, morphological, electrical and optical characteristics of the coated films were investigated. The films exhibited high carrier concentration of 1022/cc with significant reduction in resistivity of more than three order of magnitude, indicating the conversion to the nitride phase. Negative permittivity, crucial for plasmonic applications in the visible wavelength region, was verified for wavelengths > 463 nm using Drude-Lorentz model. A three-layer model was employed to verify the material’s plasmonic behaviour. The straightforward fabrication route, which combines spin-coating and ammonia nitridation at 950 °C, offers a new approach for titanium nitride films for plasmonic based gas and biosensing device applications in the visible region. In addition, for fabricating titanium nitride coatings for applications that require abrasion resistance, electrical conductivity, chemical stability, and biocompatibility.

Kinetic study on the degradation of Acid Red 88 azo dye in a constructed wetland-microbial fuel cell inoculated with Shewanella oneidensis MR-1.

Removal of Acid Red 88 (AR88) as an azo dye from the synthetic type of wastewater was studied in a laboratory-made constructed wetland microbial fuel cell (CW-MFC) inoculated with Shewanella oneidensis MR-1 (SOMR-1). Plant cultivation was implemented using a typical CW plant known as Cyperus alternifolius. The complexity of the SOMR-1 cell membrane having different carriers of electrons and H+ ions gives the microbe special enzymatic ability to participate in the AR88 oxidation link to the O2 reduction. Nernst equation developed based on analyzing the involved redox potential values in these electron exchanges is describable quantitatively in terms of the spontaneity of the catalyzed reaction. Power density (PD) at 100mg/L of the AR88 under closed-circuit conditions in the presence of the plant was 11.83 mW/m2. Reduction of internal resistance positively affected the PD value. In determining degradation kinetics, two approaches were undertaken: chemically in terms of first- and second-order reactions and biochemically in terms of the mathematical equations for rate determination developed on the basis of substrate inhibitory concept. The first-order rate constant was 0.263h-1 without plant cultivation and 0.324h-1 with plant cultivation. The Haldane kinetic model revealed low ks and ki values indicating effective degradation of the AR88. Moreover, the importance of acclimatization in terms of the crucial role of lactate was discussed. These findings suggest that integrating the SOMR-1 electrochemical role with CW-MFC could be a promising approach for the efficient degradation of azo dyes in wastewater treatment.

Preparation of adaptive bifunctional reconfigurable polymers and their sand carrying and drag reduction behaviour

AbstractIn order to solve the problem of drag reduction at the front end of shale fractures and sand carrying at the tail end with increased viscosity, the molecular dynamics simulation (MD) method was used to design polymer molecules and simulate the steric resistance, interaction potential energy, mean square displacement, and radial distribution function of the polymer. The polymer AM‐AMPS‐LMA‐DiC12AM (ASLC12) with better solubility, diffusion, and resistance reduction potential was obtained and synthesized. By scanning electron microscope (SEM) and viscoelastic analysis, ASLC12 has a stable mesh structure, good viscoelasticity, and shear resistance, and the mesh structure formed by it is in a dynamic equilibrium state of fracture‐reorganization under shear. We then analyzed the drag reduction, sand carrying, and salt resistance of ASLC12. When the concentration of ASLC12 is 0.09%, the sand‐carrying requirement is satisfied. When the concentration is 0.05%, the drag reduction rate can reach 74.1%, and the resistance reduction rate of ASLC12 in salt ion solution can still reach more than 62%. This shows that the polymer ASLC12 has better sand carrying, drag reduction, and salt resistance.

Laser-induced thermo-compression bonding for Cu–Au heterogeneous nanojoining

Abstract Surface tension-induced shrinkage of heterogeneously bonded interfaces is a key factor in limiting the performance of nanostructures. Herein, we demonstrate a laser-induced thermo-compression bonding technology to suppress surface tension-induced shrinkage of Cu–Au bonded interface. A focused laser beam is used to apply localized heating and scattering force to the exposed Cu nanowire. The laser-induced scattering force and the heating can be adjusted by regulating the exposure intensity. When the ratio of scattering forces to the gravity of the exposed nanowire reaches 3.6 × 103, the molten Cu nanowire is compressed into flattened shape rather than shrinking into nanosphere by the surface tension. As a result, the Cu–Au bonding interface is broadened fourfold by the scattering force, leading to a reduction in contact resistance of approximately 56%. This noncontact thermo-compression bonding technology provides significant possibilities for the interconnect packaging and integration of nanodevices.

Honeycomb‐Structured IrOx Foam Platelets as the Building Block of Anode Catalyst Layer in PEM Water Electrolyzer

AbstractAchieving robust long‐term durability with high catalytic activity at low iridium loading remains one of great challenges for proton exchange membrane water electrolyzer (PEMWE). Herein, we report the low‐temperature synthesis of iridium oxide foam platelets comprising edge‐sharing IrO6 octahedral honeycomb framework, and demonstrate the structural advantages of this material for multilevel tuning of anodic catalyst layer across atomic‐to‐microscopic scales for PEMWE. The integration of IrO6 octahedral honeycomb framework, foam‐like texture and platelet morphology into a single material system assures the generation and exposure of highly active and stable iridium catalytic sites for the oxygen evolution reaction (OER), while facilitating the reduction of both mass transport loss and electronic resistance of catalyst layer. As a proof of concept, the membrane electrode assembly in single‐cell PEMWE based on honeycomb‐structured IrOx foam platelets, with a low iridium loading (~0.3 mgIr/cm2), is demonstrated to exhibit high catalytic activity at ampere‐level current densities and to remain stable for more than 2000 hours.

Honeycomb-Structured IrOx Foam Platelets as the Building Block of Anode Catalyst Layer in PEM Water Electrolyzer.

Achieving robust long-term durability with high catalytic activity at low iridium loading remains one of great challenges for proton exchange membrane water electrolyzer (PEMWE). Herein, we report the low-temperature synthesis of iridium oxide foam platelets comprising edge-sharing IrO6 octahedral honeycomb framework, and demonstrate the structural advantages of this material for multilevel tuning of anodic catalyst layer across atomic-to-microscopic scales for PEMWE. The integration of IrO6 octahedral honeycomb framework, foam-like texture and platelet morphology into a single material system assures the generation and exposure of highly active and stable iridium catalytic sites for the oxygen evolution reaction (OER), while facilitating the reduction of both mass transport loss and electronic resistance of catalyst layer. As a proof of concept, the membrane electrode assembly in single-cell PEMWE based on honeycomb-structured IrOx foam platelets, with a low iridium loading (~0.3 mgIr/cm2), is demonstrated to exhibit high catalytic activity at ampere-level current densities and to remain stable for more than 2000 hours.

A highly-efficient peroxymonosulfate activator using a sewage sludge derived biochar supported cobalt oxide: Mechanism and characteristics

The application of biochar derived from sewage sludge (BS) in Fenton-like reactions for contaminant removal has attracted considerable attention. Herein, a BS-supported Co3O4 (BS-Co3O4) catalyst was synthesized using a simple two-step hydrothermal-calcination process to achieve highly efficient activation of peroxymonosulfate (PMS). The introduction of biochar effectively inhibited the aggregation of Co3O4 and reduced cobalt leaching. Compared to Co3O4, the mesoporous BS-Co3O4 exhibited an 8-fold increase in specific surface area (SSA) to 111.92 m2∙g−1, and a 46 %-66.4 % reduction in crystal plane size. The interaction between biochar and cobalt oxide resulted in several notable enhancements in the BS-Co3O4 composite. Specifically, there was an increase in sp2 carbon content, a 42.69 % rise in capacitance, and a 79.99 % reduction in charge transfer resistance. These improvements contributed to enhanced PMS activation performance. The BS-Co3O4 also contained a higher content of Co(II), sp2 carbon, and oxygen vacancies (OV). Co(II) played a crucial role in the redox reaction, accelerating the formation of SO4•− and 1O2 during the PMS activation process. Additionally, OV acted as electron capture centers, further promoting the generation of 1O2. Evidence from reactive species investigations and electron paramagnetic resonance (EPR) tests indicated that SO4•− and 1O2 were the main reactive radicals for eliminating tetracycline (TC). Based on the identification of TC intermediates, two potential degradation pathways were proposed, and a reduction in intermediate toxicity was observed. Experiments involving interference and repetition demonstrated that the BS-Co3O4 catalyst was stable and reusable. This work provides a solution with low metal leaching, high recycling performance, and safety for antibiotic wastewater treatment.

Numerical and experimental study on the mechanism of added resistance in stepped moonpool under different waves

To study the additional resistance effect of the moonpool during the navigation of the drilling vessel, this paper explores the variation of the drilling vessel resistance under different waves based on a model test and numerical simulation. The difference between the model test and the numerical simulation results is compared, and the mechanism of the added resistance of the moonpool under different waves is revealed. The results show that the technology of numerical simulation is able to accurately simulate the navigation resistance of the drilling vessel in waves. The numerical simulation results closely correspond to the experiment results, and the error range can be controlled within 10%. In the components of the total resistance of the hull, pressure resistance plays a dominant role when the drilling vessel sails in waves. The pressure resistance accounts for about 60%–70% of the total resistance, while the friction resistance accounts for about 30%–40% of the total resistance. At low speed, the average resistance reduction rate of the dissipative equipment is 4.4%; under the condition of medium speed, it is 7.5%; at high speed, it is 9.6%; and the resistance reduction efficiency of the dissipative equipment increases with the increase in speed. The dissipative equipment partially suppresses the eddy's action stage and prevents eddy shedding from entering and directly hitting the back wall, thereby reducing the moonpool's additional pressure resistance. The research results can provide a reference for energy savings and emission reductions in drilling vessels.

Development of High Performance Light Weight Concrete through incorporation of Steel Fibers onto Polyurethane Foam Concrete

A lightweight, high-performance concrete was developed using steel Fiber-reinforcement onto polyurethane foam (PUF) enhanced lightweight concrete. Fiber-reinforcement enhances strength parameters of concrete. But, the interaction between polyurethane foam’s ability to reduce density and the reinforcing effects of steel Fibers in terms of mechanical strength, shrinkage, chloride penetration, and crack resistance has not yet been explored. To overcome this limitation, investigations were done in this study to find compressive strength, split tensile strength, flexural strength, shrinkage, impact resistance, and chloride ion penetration on PUF incorporated with steel Fibers. Microstructural analysis was performed using scanning electron microscopy (SEM) to examine Fiber-concrete bonding. The results revealed that mixes with 1.5% steel Fiber content exhibit good performance, in terms of improved compressive and flexural strengths, impact resistance, and shrinkage reduction. Chloride penetration test results exhibited good chloride resistance in Fiber-reinforced mixes, making them suitable for use in corrosive environments. SEM analysis confirmed that the improved mechanical properties were largely due to enhanced Fiber-matrix bonding, which contributed to better crack control. Thus, this study was able to develop a Polyurethane foam light weight concrete incorporated with steel Fibers which could synergistically enhance its strength and durability characteristics.

Insights into the ternary substitution Na2.96+xK0.04 V2-xNix(PO4)2.98F0.06 with superior rate capability and near-zero strain property

Na3V2(PO4)3 (NVP) is considered the most favorable cathode for sodium-ion batteries due to its solid NASICON skeleton. Nevertheless, poor intrinsic conductivity is insufficient for its further commercialization. In this paper, we present a promising K/Ni/F co-doped and carbon nanotubes (CNTs) encapsulated Na2.96+xK0.04 V2-xNix(PO4)2.98F0.06 (KNF@CNTsx) cathode materials. The synthesis of KNF@CNTsx is achieved using a facile sol-gel method. The replacement of Na+ with K+ broadens the migratory pathway and supports the crystal skeleton, while F− substitution reduces the average grain dimension, thereby increasing the diffusion rate of Na+. Furthermore, the reduction of resistance by Ni2+ doping enables optimization of the transport of electrical charge, while also facilitating the optimization of chemically-defined properties. Concurrently, the optimal quantity of carbon capping and wrapping of CNTs facilitate the formation of efficacious conductive network, which diminishes the size of grains and shortens the pathway for the diffusion of Na+. This network could also serve as a buffer against crystal deformation. In conclusion, the modified KNF@CNTsx samples exhibit notable enhancements in their conductivity, ion diffusion capacity, and structural stability. Among them, the KNF@CNTs0.04 sample exhibits a capacity for reversibility of 93.3 mAh g−1 at 50C, with a remaining capacity of 68.5 mAh g−1 after 4000 successive long charge-discharge cycles. Ex-situ electrochemical XRD demonstrates the V3+/V4+ redox reaction occurs accompanied by the phase transfer reaction, during which Na+ prefers to diffuse along c-axial in the crustal structure. Moreover, volume alteration of this KNF@CNTs0.04 cellular entity is miniscule and reversible during the charge-discharge process, further confirming the stabilized construction and near-zero strain property. The after-cycled XRD/SEM/XPS certify the improved chemical and structural stability of KNF@CNTs0.04, indicating the constructive effects of K/Ni/F ternary substitution.

A three-stage oxidation method improves sludge dewaterability by achieving sustained oxidation and phased enhanced coagulation: Ingeniously using H2O2 as a “converter”

Sludge reduction is essential for mitigating the environmental hazards associated with sludge. The use of ferric chloride (Fe(III)) catalyzed ferrate (Fe(VI)) can significantly enhance sludge dewaterability by increasing the Fe(VI) oxidation rate and maintaining in-situ enhanced coagulation. However, its weak oxidation ability at the sludge’s original pH limits its practical application. To address this, hydrogen peroxide (H2O2) strengthened Fe(VI)/Fe(III) was employed to efficiently improve sludge dewaterability without pH adjustment, thereby enhancing the environmental utilization capacity of sludge. Compared to raw sludge, the treatment of Fe(VI)/Fe(III)–H2O2 resulted in approximately the 95% reduction in specific resistance to filtration (SRF) and increased the bioavailable phosphorus (P) content in dewatered sludge. During the oxidation process, highly reactive species such as tetravalent iron (Fe(IV)) and hydroxyl radicals (OH) were generated, facilitating the release of tightly bound water in extracellular polymeric substances (EPS). Importantly, the oxidation process was divided into three stages (persistent moderate oxidation — fast strong oxidation — sustained weak oxidation) based on the predominant reactive species (Fe(IV) or OH). This division promoted more robust and more durable oxidation processes. Phased enhanced coagulation occurred during the oxidation process. The gradual increase in Fe(III) content led to the re-flocculation of damaged EPS, enlarging the size of sludge drainage pores/channels and improving water discharge efficiency. Additionally, the costs and carbon emissions of chemicals for the Fe(VI)/Fe(III)–H2O2 process were 18% and 52% lower than those of the traditional Fenton method. This study not only achieves the goals of sludge reduction and resource collection but also provides insights into selecting sludge conditioning methods that meet pollution reduction and carbon emission reduction requirements.

Construction of electron-deficient Co on the nanoarrays enhances absorption and direct electron transfer to accelerate electrochemical nitrate reduction

Electrochemical nitrate reduction is a promising remediation strategy for nitrate-contaminated wastewater treatment, in which nitrate adsorption is a prerequisite step in the overall process. Herein, the iron-induced cobalt phosphide was grown in situ on porous nickel foam (Fe-CoP/NF) for the electrochemical nitrate reduction. Structural characterization verified doping of Fe and the uniform nanotube arrays of Fe0.03CoP/NF. Remarkably, the Fe0.03CoP/NF exhibited a high efficiency nitrate removal efficiency (99.3%) and excellent ammonia selectivity (100% selectivity and 0.485mg·h-1cm-2 NH3 yield rate). Both experimental and theoretical results reveal that Fe doping alters the local charge distribution of the Co active centers to form electron-deficient Co. The Co electron-deficient regions were constructed due to the difference in electronegativity between Co and Fe. Furthermore, the formation of electron-deficient centers facilitates the reduction of charge transfer resistance. In particular, Fe0.03CoP/NF maintained an excellent conversion efficiency of nitrate to N2 (99.8%) with 60mM Cl−, and the selectivity of N2 is maintained above 99.1% during long-term operation. This system possesses a low electrical consumption of 1.79 kWh·molN-1. This study designed an enhanced electrocatalyst through enhanced nitrate absorption and direct electron transfer strategies, thus providing a promising and low-power consumption approach for addressing nitrate pollution.

Defect engineering design and electrical breakdown model improve dielectric properties and reliability of rare-earth doped BaTiO3-based ceramics

The incorporation of rare-earth elements into BaTiO3-based multilayer ceramic capacitors (MLCCs) plays a pivotal role in enhancing the dielectric constant and reliability. In this study, The BaTiO3-based ceramics doped with La and Dy were prepared separately and their dielectric properties and reliability were thoroughly compared. The La-doped sample exhibited a significantly enhanced dielectric constant, which can be attributed to the short-range migration of liberated oxygen vacancies () facilitated by the incorporation of defects -. However, the presence of free in the La-doped sample led to a significant reduction in insulation resistivity during the initial application of the electric field. Microstructural analysis of the failure points resulted in the proposal of an electrical breakdown model, which elucidates the superior breakdown strength observed in the La-doped sample. This study provides novel insights for the development of MLCCs with high dielectric constants and high reliability.

Exploring the hardness-independent wear behavior of typical wear-resistant materials under dynamic and static conditions

In this study, three types of wear-resistant materials including high-chromium cast iron (HCCI), medium-chromium cast steel (MCCS), and low-chromium cast steel (LCCS), with similar macroscopic hardness but distinct microstructures and impact toughness have been prepared. The wear behavior of these three materials under different loads were investigated by impact wear experiments under dynamic load and three-body wear experiments under static load. The results revealed that the almost fully martensitised MCCS had the least mass loss under low dynamic impact load wear conditions. The brittleness associated with large carbides intensified with increasing impact load, culminating in a significant reduction in the impact wear resistance of HCCI. The residual austenite rapidly transformed into martensite, thereby effectively improving the wear resistance of the LCCS. Comparatively, the experimental steels were all characterized by fatigue wear of the abrasive on the material surface under static wear conditions at low loads and showed similar wear resistance. Conversely, the large carbides demonstrated superior wear resistance under conditions of high static load, and HCCI had the best wear resistance.

A bio-inspired liquid-like smooth copolymer coating with superior biofouling resistance and drag reduction

A bio-inspired liquid-like smooth copolymer coating with superior biofouling resistance and drag reduction

Optimizing Well Integrity with Accurate Forecasting of Casing and Tubing Resistance Reduction Trends Through Innovative Numerical Modeling Techniques

Summary Well integrity is an essential aspect of well operations, and international standards are stringent on its application. Tubing and casing corrosion constitutes a major risk to well integrity and a challenge that must be analyzed preventively. Corrosion logs are programmed to verify the status of the barriers, but there is currently no methodology for planning future logs. In this paper, we propose a numerical modeling method to forecast tubular resistance reduction trends and estimate the barrier’s residual life. Corrosion logs are expensive and require the well to be shut in, which impacts the cost of the operation. Therefore, a numerical methodology for planning future logging is preferable to planning based on experience. Here we propose a methodology for predicting the point at which the downhole barriers will no longer satisfy the maximum allowable annular surface pressure (MAASP) criteria, using data from historical corrosion logs and a time-linear corrosion model. This innovative methodology recalculates MAASP for collapse and burst resistance of corroded pipes while considering well completion design and vertical depths resulting from the directional survey. The proposed methodology provides a comprehensive assessment of the corrosion progress, making it a more reliable tool for forecasting future corrosion trends. The methodology uses the last two corrosion logs for optimal prediction, but it also works when a single corrosion log is available. Numerical modeling is then used to calculate pipe resistance at each depth step of the LAS file, drawing a picture of the resistance vs. depth and time. The result of this new method is a chart that forecasts the progressive reduction of A-Annulus MAASP and the time at which it will cross the minimum criteria of the operator. Furthermore, the proposed methodology provides a probability window that takes into consideration the best- and worst-case scenarios. This is the first time that numerical modeling is used to recalculate MAASP and to forecast MAASP reduction trends in well barriers, based on corrosion/erosion measurements. The corrosion logging schedule can, hence, be programmed before MAASP reaches the operator’s limit, thus optimizing planning and costs for the operator. This, in turn, leads to a reduction in costs without affecting the overall operability and risking barrier failures.

Beyond Conventional Drug Design: Exploring the Broad-Spectrum Efficacy of Antimicrobial Peptides.

In the fight against pathogenic infections, antimicrobial peptides (AMPs) constitute a novel and promising class of compounds that defies accepted drug development conventions like Lipinski's rule. AMPs, often known as nature's antibiotics, are remarkably effective against a variety of pathogens, including viruses, bacteria, parasites, and fungi. Their effectiveness, despite differing from traditional drug-like properties defies accepted standards. This review investigates the complex world of AMPs with an emphasis on their structural and physicochemical properties, which include size, sequence, structure, charge, and half-life. These distinguishing characteristics set AMPs apart from medications that adhere to Lipinski's rules and greatly contribute to their selective targeting, reduction of resistance, multifunctionality, and broad-spectrum efficacy.

Cardiovascular Effects of a Glycosylated Flavonoids-Rich Leaf Extract from Brazilian Erythroxylum campestre: A Potential Health Bio-Input

Background: Bioactivity assessments of plant-derived products can benefit human and animal health, especially in regions with vast plant diversity. This study focused on chemical and cardiovascular analyses of Erythroxylum campestre A. St. Hil. leaf extracts. Methods: High-performance liquid chromatography, liquid chromatography coupled with mass spectrometry, and nuclear magnetic resonance spectroscopy were used to elucidate the structures of the flavonoids in E. campestre. The E. campestre methanolic fraction (ECM-ppt-M; at doses of 1, 2, 3, and 6 mg∙kg−1 or vehicle) was administered intravenously to normotensive and spontaneously hypertensive rats (SHRs), and we recorded the mean arterial pressure (MAP), heart rate (HR), renal vascular resistance (RVR), and aortic vascular resistance (AVC). Results: The ECM-ppt-M extract demonstrated significant antihypertensive activity, as evidenced by reductions in MAP, RVR, and AVR, with effects that were particularly pronounced in SHRs. Following the establishment of these cardiovascular effects, phytochemical analysis revealed the presence of glycosylated flavonoids, which are likely contributors to the observed antihypertensive properties of the extract. Conclusions: The notable reductions in MAP and vascular resistance observed with ECM-ppt-M treatment suggest its antihypertensive effect. These findings demonstrate the potential therapeutic value of this extract with regard to the treatment of hypertension. Future studies on ECM may provide a promising therapeutic alternative capable of reducing the risk of toxicity and adverse effects associated with synthetic drugs.

Influence of phase composition and stress on the corrosion behavior of metastable β titanium alloy Ti-5Mo-5V-6Cr-3Al in 15 wt% HCl solution

Immersion experiments, electrochemical tests under different tensile stresses, and microstructure observation using SEM, EBSD, and TEM were carried out on three Ti-5Mo-5V-6Cr-3Al alloys with different phase compositions in 15 wt% HCl solution to clarify the effects of the phase compositions and stresses on the corrosion behavior of metastable β-titanium alloys in acidic media. The microstructure with only primary α-phase on the β-matrix (No. M1) presents the smallest corrosion current density and the highest corrosion potential, indicating relatively the best corrosion resistance; the microstructure with both primary and secondary α-phase on the β matrix (No. M2) has moderate corrosion resistance; and the microstructure with secondary α-phase precipitated on the β matrix (No. M3) has the relatively poorest corrosion resistance. The results of the immersion experiments show the same regularity as the electrochemical tests. The corrosion resistance of all three microstructures decreases as the degree of stress loading increases. The apparently small amount of α-phase content in M1 is the reason for the difference in corrosion resistance between M2 and M3, M3 alloys with larger average grain sizes exhibit better corrosion resistance than M2 alloys. Under tensile loading, disruption of the surface passivation film and pitting promoted by dislocation slip are the main reasons for the reduction in the corrosion resistance of the alloy.