Immersion Time Research Articles

Tailoring the mechanical strength and corrosion resistance of aluminum matrix composites through biochar reinforcement at varied weight percentages

This study introduces an innovative approach to fabricate aluminum matrix composites strengthened with biochar, derived from renewable biomass sources. A systematic investigation of varying biochar weight percentages (0, 2.5, 5, 7.5, and 10 wt%) reveals substantial improvements in mechanical properties and corrosion resistance. Mechanical assessments, including compressive strength and hardness, demonstrate a significant enhancement in mechanical strength with biochar incorporation. In this study, it was discovered that the composite with 7.5 wt% biochar exhibits an optimal balance, displaying an 8.83% increase in compressive strength and a 15.15% rise in hardness compared to the base aluminum matrix. The study further evaluates corrosion behavior through electrochemical analyses and immersion tests in 3.5% NaCl corrosive environments, highlighting the superior corrosion resistance of biochar-reinforced composites. Corrosion rates decrease by 73% in the composite with 10 wt% biochar for the 24 h immersion time, affirming its protective barrier against corrosive agents. This research provides quantitative insights into tailoring mechanical and corrosion properties in aluminum matrix composites through biochar reinforcement, offering a promising avenue for sustainable material development. The resulting materials exhibit not only an 8.83% increase in mechanical strength but also a 73% reduction in corrosion rates, offering valuable uses in industries that need strong, eco-friendly solutions.

Effect of environmental factors on adsorption of ciprofloxacin from wastewater by microwave alkali modified fly ash

Antibiotics, as emerging persistent pollutants, pose significant threats to human health. The effective and low-cost removal of ciprofloxacin (CIP) from wastewater has become an important research focus. In this study, fly ash (FA) was used as the raw material, and modified fly ash (MFA) was prepared by varying microwave power, alkali concentration, and immersion time to investigate its adsorption characteristics for CIP. Results showed that the optimal preparation conditions for MFA with the most effective adsorption of CIP, using the Box-Behnken response surface methodology, were a microwave power of 480 W, an alkali concentration of 1.5 mol/L, and a modification time of 3 h. Scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction analyses revealed that after modification, the glassy structure of FA is destroyed, the specific surface area is increased, and obvious hydroxyl O–H absorption peaks appear. Both FA and MFA exhibited adsorption processes for CIP that conformed to pseudo-second-order kinetics and the Langmuir equation. Maximum adsorption of CIP (9.61 and 12.67 mg/g) was achieved at pH = 6. With increasing temperature, the adsorption capacity of both FA and MFA for CIP decreased, indicating an exothermic process. The adsorption capacity of CIP decreased with increasing ion concentration, with the impact order of ions being Al3+ > Ca2+ > Na+. The results show that pore filling, electrostatic interaction, ion exchange and complexation are the main ways of CIP adsorption by FA. Microwave alkali modified fly ash is an economical and efficient adsorbent for CIP removal in water, realizing the purpose of “treating waste with waste”. This study provides a scientific basis for controlling CIP treatment in wastewater.

A Comprehensive Review of Small Particle Reagent Efficacy in Developing Latent Fingerprints Immersed in Water: An Empirical Analysis

A latent fingerprint is a shred of inevitable evidence left on a scene of the crime by the offender. Being aware of fingerprints, offenders tend to deteriorate all possible pieces of evidence by different methods that include burning, immersing the evidence in water, and many more. Water-immersed latent fingerprints are still viable for the development process due to the presence of water-insoluble components (Lipids, oils, etc.) in the latent fingerprint. Different methods have been tested for the imaging of water-immersed latent fingerprints among which Small Particle Reagent (SPR) was found to be the most efficient by many researchers. This method involves the application of fine particles suspended in a reagent based liquid medium onto the surface containing latent prints immersed in water, resulting in the development of highly detailed fingerprint impressions. The reagent comprised of hydrophobic head and hydrophilic tails that adhere to latent fingerprint and suspended particle respectively and thus act as a junction among them. The diverse composition of Small Particle Reagent, various surfaces for taking impressions of latent fingerprint (followed by immersing in water), the Shelf life of SPR, immersion time of latent fingerprint, and various immersion medium studied by researchers has been reviewed in this paper. The maximum shelf life of SPR reported by a researcher is 6 months and the maximum immersion time is 45 days. Furthermore, the need for green synthesis of SPR is emphasized due to its toxicity caused by long-term exposure.

Experimental investigation on the impact of water immersion time and particle size on the ignition characteristics of coal dust

After drying, water-immersed coal is more prone to spontaneous combustion than raw coal. However, the influence mechanisms of particle size and water immersion duration on the physicochemical properties of coal dust, as well as the explosion and fire hazards of water-immersed coal dust, have not been sufficiently investigated. In this study, two particle sizes of coal dust were selected, and experiments were conducted using the Godbert-Greenwald furnace, Hartmann tube, Muffle furnace, and Fourier Transform Infrared Spectrometer. The study investigated the impact of different water immersion times, dust particle sizes, and dust concentrations on the sensitivity of coal dust fires and explosions, analyzed the process of functional group changes in coal dust particles in water and other mechanisms of transformation. The results indicated that the water immersion process increased the number of active functional groups on the surface of coal dust, significantly reducing the Minimum Ignition Temperature (MIT) and Minimum Ignition Energy (MIE) values for different samples, and also enhancing the ignition sensitivity and peak temperature of coal dust layer fires. This study contributes to a deeper understanding of the characteristics of coal dust and is of great significance for improving the prevention and control of coal dust fires and explosions.

Unveiling the Therapeutic Potentials of Water Hyacinth (Eichhornia crassipes (Mart.) Solms) Flower against Oxidative Stress, Inflammation and Depressive Disorders: GC-MS/MS, In Vitro, In Vivo and In Silico Approaches.

Water hyacinth (Eichhornia crassipes (Mart.) Solms) is a highly invasive aquatic weed native to the Amazonia basin, known for its rapid propagation, adaptability and utilization in traditional medicine. The study aims to unveil the therapeutic potential of water hyacinth flowers methanolic extract (EC-CME) and its four kupchan fractions (EC-PESF, EC-DCMSF, EC-EASF, EC-ASF) through diversified chemical-pharmacological approaches. GC-MS/MS of EC-CME uncovered a rich tapestry of 72 phytochemical components. In vitro DPPH scavenging assay and total phenolic content determination assay deciphered promising antioxidant assays with remarkably low IC50 values of 0.353 and 0.485 µg/mL, respectively for EC-ESF and EC-ASF. Besides, different in vivo tests, including tail emersion, acetic acid-induced writhing, and thiopental-induced sleeping test of EC-CME, yielded a remarkable 8.61 ± 0.29 minutes of tail immersion time compared to the control's 2.05 ± 0.11 minutes at the highest dose (600 mg/kg). The best % inhibition of writhing was recorded as 47.96% accrued in 400 mg/kg dose, indicating robust pain-relieving properties. The onset and duration of sleep are significantly ameliorated for EC-CME, unveiling its antidepressant potential. Besides, molecular docking studies along with ADME/T analysis also validated the wet lab findings as well as their safety, efficacy and drug-likeliness profile.

Assessing the impact of corrosive acids on human bone integrity in forensic context.

Dissolving bodies is a contemporary method of disposing of human remains and has been practiced throughout the years. This research article discussed the impact of readily available corrosive chemicals, such as Hydrochloric acid (HCl), Sulfuric acid (H2SO4), and Expelz™ toilet cleaner, on human bone. Unfortunately, the existing literature on this subject is scarce, with only a few studies conducted on human bones. To address this gap, we conducted an experimental analysis using human sternum bone fragments. These samples were subjected to immersion in different acids, namely HCl and H2SO4, at two concentrations (10% and 37%), and Expelz™ toilet cleaner. This research aims to describe the impact of toilet cleaner, sulphuric acid, and hydrochloric acid on bone tissue deterioration at various time intervals. Further, the morphological alterations weight loss, and cytological analysis of bone tissue residue with various acid concentrations and immersion times (3.5, 9, 24, 36, 48, 60, and 72h) were analyzed. Among the chemicals examined, it is evident that 37% hydrochloric acid (HCl) and sulfuric acid (H2SO4), regardless of refreshment, exhibit the highest reactivity, resulting in the complete decomposition of hard tissue within a few hours. In contrast, the behaviour of 10% H2SO4 reveals a more intricate degradation process characterized by fluctuations in weight loss. These distinct reactivity profiles under different conditions are crucial in understanding the potential for rapid weight loss, signifying high reactivity and more gradual weight loss, indicating a faster decomposition rate. Notably, refreshment of the solution enhanced the reactivity of both HCl and H2SO4.

Effect of static magnetic field on corrosion of X70 pipeline steel in dilute sodium bicarbonate solutions

This paper focuses on the effect of a 0.1 T static horizontal magnetic field on the corrosion of X70 pipeline steel in 0–0.05 mol/L sodium bicarbonate solutions. The weight loss data indicate that the magnetic field reduces the average corrosion rate during immersion within 48 h in all the test solutions. The magnetic field tends to increase the average corrosion rates for the immersion time of 72 h and 96 h. The magnetic field increases the proportion of magnetite in corrosion products formed on the specimen of immersion in 0.05 mol/L sodium bicarbonate solution for 168 h. The open-circuit potentials (OCP) are in the active zone of the E-pH diagram within 48 h immersion with 0 T and 0.1 T magnetic field. A 0.1 T magnetic field delays the process for the electrode to enter the passive zone of the E-pH diagram. The linear polarisation resistance (LPR) data shows that the resistance of the active zone with 0.1 T magnetic field is larger than that with 0 T. The electrochemical impedance results also indicate that the electrode is in an active state when the potential is below −700 mVSCE and in a passive state when the potential is above −200 mVSCE.

SiC-BASED CERAMICS AS A CONTAINER MATERIAL FOR DEEP GEOLOGICAL DISPOSAL OF RADIOACTIVE WASTE

In this work the research of Cr-doped SiC ceramics as a promising material for containers for the deep geological disposal of radioactive waste was carried out. Samples were investigated using XRD, Raman spectroscopy, microhardness measurements, nanoindentation and corrosion resistance tests. Obtained results showed that addition of 0.3…0.7 wt.% of Cr improves the mechanical properties of SiC ceramics. Corrosion tests in distilled water at T = 90 °C and immersion time of up to 4300 h revealed that Cr addition slows down corrosion processes in SiC ceramics. The average dissolution rate of SiC(Cr) samples in water is quite low and does not exceed the value of 0.16 μm/year.

Comparison of thermogravimetry response of alkali-activated slag and Portland cement pastes after stopping their hydration using solvent exchange method

AbstractThe critical step for any subsequent instrumental analysis of cementitious binders is to stop their hydration reactions, i.e., to remove free water. One of the most available techniques is a solvent exchange method. However, the solvents are known to be strongly bound in ordinary Portland cement (OPC) paste and alter the results of thermogravimetric analysis (TGA) and sensitive hydrates, while their effect on TGA response of alkali-activated slag (AAS) has not been comprehensively investigated. Therefore, the objective of this paper is to track the effects of fundamental aspects of the solvent exchange on the TGA response of AAS with different sodium activators (hydroxide, carbonate, waterglass) and to support these results by X-ray diffraction and effluent gas analysis. All solvents used (acetone, diethyl ether, isopropyl alcohol, ethanol, and methanol) affected the TGA response of all tested pastes, and their effect was enhanced by prolonged immersion time. All solvents induced an additional mass loss at around 800 °C and, especially for OPC paste, increased in situ carbonation, even in an inert atmosphere. Methanol and ethanol had a detrimental effect on ettringite and decreased the basal distance of the C–(A)–S–H gel, while they only marginally affected gaylussite. For AAS, hydration stoppage by washing out the alkali-rich pore solution with water was also investigated and can usually be recommended (except for its detrimental effect on gaylussite), as it is more efficient than organic solvents, which lack solubility for activators. Methanol and ethanol are the most suitable alternatives, particularly for NaOH.

Evaluation of Passive Films on 17-7PH and 410 Stainless Steel Exposed to NaCl Solution.

This work covers the formation of a passive state for two different alloys used in the aeronautical industry. The aim of this study is to investigate the effectiveness of passivation treatments on 17-7PH and 410 SS (stainless steel) samples, specifically when performed with citric and nitric acid solutions at 49 °C using an immersion time of 90 min and subsequent exposure in 3.5 wt.% NaCl solution. Employing the cyclic potentiodynamic polarization (CPP) technique, the corrosion properties of the passivated material were evaluated according to the ASTM G65-11 standard. A microstructural analysis was performed using scanning electron microscopy (SEM). The passivated layer was characterized via X-ray photoelectron spectroscopy. In the results, the CPP curves showed positive hysteresis, indicating pitting localized corrosion, and 17-7PH steel passivated at 49 °C for 90 min in citric acid exhibited lower corrosion rate values equivalent to ×10-3 mm/year.

Evaluating the bio-functionalities of Ti-6Al-7Nb alloy after surface modification using electrical discharge machining

The present work evaluates the influence of surface modification on the bio-functionalities of Ti-6Al-7Nb alloy in terms of apatite formation, metal ion release rate and anti-bacterial activities. The surface modification in the form of change in surface integrity, and increases in the exposed surface area, has been achieved using wire-electrical discharge machining (WEDM) and electrical discharge μ-drilling(EDD). Due to high discharge energies, molten material will deposit on the parent material (recast layer), which increases the surface roughness (parent surface 0.5 μm to 2.34 μm) and hardness (patent material 304VH to 385VH) after subsequent re-solidification and quenching. Surface roughness and hardness near the micro-drilled hole are observed to increase. After surface modification, the apatite formation is increased on Ti-6Al-7Nb alloy with increasing immersion time and the ion released rate was found lowest on the WEDMed surface as compared to micro drilled and polished surface. Field-emission electron scanning microscopy (FESEM) and energy dispersive x-ray spectroscopy (EDAX) observations confirmed the presence of phosphate and calcium ions on the WEDMed surface and nearby the micro-drilled surface. The variation in colour of the simulated body fluid (SBF) after the immersion of WEDMed, EDD, and polished samples indicates the variable effecton pH levels of the SBF solution for three types of samples.The anti-bacterial bioactivity of Ti-6Al-7Nb was found to be better on the WEDMed surface as compared to polished surfaces, which is due to the formation of a rutile-TiO2 layer on WEDMed surface.

The color stability of artificial white spot lesions treated with resin infiltration after exposure to staining beverages

BackgroundTo evaluate the effect of staining beverages on the color-changing of resin-infiltrated artificial white spot lesions (WSLs).MethodsThirty-five artificial WSLs were created by pH cycling on flat bovine teeth specimens. The WSLs were treated with resin infiltration and were divided into five groups based on staining beverages: artificial saliva, coffee, wine, green tea, and Coca-Cola. These specimens were subjected to a 28-day exposure to the respective beverages. Color stability was assessed using a spectrophotometer at different time points: baseline, after 7, 14, 21, and 28 days of exposure, and repolishing. The color difference (∆E) between each time point and the baseline was calculated. Statistical analysis was performed using two-way measures ANOVA with a significance level of p = 0.05.ResultsAll resin-infiltrated specimens exposed to staining beverages for 7 days exhibited more significant color changes than those exposed to artificial saliva. The color change patterns varied based on the type of beverage. The color alterations intensified with extended immersion in the wine and Coca-Cola groups, while there were no significant differences in the color of specimens after 28 days of immersion in the coffee and green tea groups. However, after cleaning with pumice powder, all specimens showed significantly reduced color changes compared to those observed after 28 days of immersion, except those immersed in coffee.ConclusionsExposure of resin-infiltrated bovine tooth specimens to staining beverages resulted in a significant color alteration as the immersion time increased. However, the staining effect could be minimized by cleaning with pumice powder, except for the coffee group.Clinical relevanceAfter resin infiltration treatment, patients should be advised to minimize the consumption of colored beverages to prevent staining that could impact esthetic appearance.

Molybdate and vanadate ions as corrosion inhibitors for clad aluminium alloy 2024-T3

Molybdate and vanadate ions were used as corrosion inhibitors for the clad aluminium alloy 2024-T3 in chloride solution to investigate the differences in their inhibitory effect. Electrochemical measurements in 0.1 M NaCl investigated the influence of inhibitor concentration from 0.5 mM to 250 mM, solution pH from 5 to 9 and immersion time at open circuit potential of up to 12 h. Both compounds act predominantly as anodic inhibitors; however, the effect of molybdate increases significantly at concentrations above 50 mM and leads to a broad passive range. Surface analysis of the samples exposed to inhibitor performed by X-ray photoelectron spectroscopy showed that the inhibitor layers consist of oxides of multiple valences. Scanning electron microscopy with chemical analysis was also used to characterise the inhibitor layers. Equilibrium diagrams of the aqueous species in the selected concentration range were generated to better understand the inhibition mechanism and to correlate the electrochemical data and data on surface properties.

True-triaxial strength characteristics of cement stone subjected to sulfuric acid corrosion: An experimental and theoretical study

True triaxial tests were conducted to investigate the effect of sulfuric acid corrosion on the true triaxial strength of cement stone under different acid immersion times, including the common loading path and novel loading path with constant Lode angle. The chemical composition and microstructure of cement stone under different acid immersion times (0, 7, 14, and 28 d) were examined via X-ray diffraction and scanning electron microscopy. As the duration of acid immersion increases, the concentrations of portlandite (Ca(OH)2) and calcium silicate hydrate (C-S-H) within the cement stone exhibit a gradual decline, while the presence of calcium sulfate (CaSO4) progressively rises. The microstructure of the cement stone was primarily affected by two factors: the damaging and strengthening effects of sulfuric acid and CaSO4, respectively. The damaging effects of the acid were dominant for days 0–14 of immersion, with continuous increase in microstructure damage. Subsequently, the strengthening effect of CaSO4 became apparent for days 14–28 of immersion, with continuous improvement in microstructure integrity. Consequently, the strength of cement stone exhibited a diminishing trend during the initial immersion period of 0–14 days, followed by an enhancement in strength from 14 to 28 days of immersion. Furthermore, a three-dimensional strength criterion was proposed by combining the Hoek–Brown and Matsuoka–Nakai criteria. The failure envelope first shrank and then expanded with increasing immersion time, accurately describing the variation in strength in the three-dimensional principal stress space.

Effect of heat treatment on chemical durability and TL dosimetric properties of Na2O-SrO-B2O3 glass system

Na2O-SrO-B2O3 glass system prepared by the known melting-quenching method was applied to a progressive heat treatment (HT) at 600 °C for 4, 6, 8 and 10 h. Glass (G) and its corresponding heat treated (HT) samples were characterized by density, molar volume and XRD technique that revealed the complete amorphous structure of the glassy matrix and the coexistence of two crystalline phases in the corresponding glass ceramics; monoclinic phase of NaSrBO3 and the triclinic phase of sodium strontium pentaborate Na3SrB5O10. Testing chemical durability of G and HT samples at 95 °C for 24 h, revealed higher chemical stability in aqueous (H2O) and acidic (H2SO4) solutions, while the highest leachability was detected in the alkaline medium (NaOH). pH of leaching solution was found to control the leaching process and displayed rising behavior with time of immersion. The progressive rising of leaching solution temperature; 25, 40, 60 and 95 °C, revealed a quiet leachable enhancement as well. SEM photographs represented rough and heterogeneous surface morphology with continual leaching and the formation of colloidal layers at the later stages of corrosion.The TL-dosimetric properties indicated extremely higher thermoluminescence properties of HT samples than the untreated glass. The analysis of the exhibited TL signals revealed the composition of the glow curves of the treated and untreated samples of eight TL components. The obtained results recommend the acceptable chemical durability of the heat treated samples especially in the neutral medium that displayed no more than 8.5% leachability rate yearly, besides their promising TL-dosimetric features, accordingly their possible application in the field of radiation dosimetry.

Galvanic Corrosion Behavior of Zn and Al Couples in NaCl Solution

Multi-materialization is being promoted in automotive structural materials, and fuel economy is being improved by replacing steel with aluminum and other lightweight metallic materials. Automotive steel is often galvanized for corrosion protection, and galvanic corrosion of aluminum and zinc in an atmospheric environment is a very important issue in evaluating automotive durability. Zinc is usually considered to be an anode when combined with aluminum, but its galvanic corrosion behavior can be complicated by environmental conditions because the corrosion potentials of the two are relatively close. Therefore, the objective of this study is to investigate the galvanic corrosion behavior of the couples consisting of zinc and aluminum under corrosive environmental conditions.The galvanic couple used in this study was fabricated from AA1050 Al and zinc plates. The width and length of both plates are 10 mm and 15 mm, respectively. After connecting lead wires to each plate, both plates were embedded in epoxy resin. To fabricate coplanar galvanic couples in this study, both plates were placed separately along the surface from a gap size of 500 um. The surfaces of the galvanic pairs were polished with SiC paper to JIS 2000 grit and cleaned with EtOH. The test solutions used in this study were aqueous NaCl solutions of various concentrations from 0.01 to 2 M, prepared with Milli-Q water and reagent grade chemicals. Galvanic currents and corrosion potentials were measured to investigate the galvanic corrosion behavior of the couples after 72 hours of galvanic corrosion experiments in the test solutions.The results of the galvanic corrosion test showed that the immersion potentials of the galvanic couples were lower at higher NaCl concentrations. The galvanic current decreased with immersion time, finally reaching about 1 uA in all NaCl solutions. The results of the electrochemical impedance measurements for galvanic couples in various NaCl concentrations showed that the impedance gradually increased with immersion time. It was also found that the impedance can be expressed as an electrical equivalent circuit consisting of two time constants, and that the impedance increases at intermediate frequencies between 0.1 and 1 Hz, which is thought to correspond to the dissolution reaction of Zn. This was the same trend as the behavior of the galvanic current. These results suggest that prolonged immersion reduces the galvanic current and the dissolution rate of zinc due to the passivation of the A1050 surface and the suppression of cathodic reactions.

Comparing the Corrosion Behavior and Microstructure of a WE43 Mg Alloy in Simulated Body Fluids Under Different CO2 Conditions

With the low density and high specific strength, magnesium (Mg) alloys are lightweight alloys with various applications. In addition, combined with biocompatibility, similar mechanical properties to human bones, and unique biodegradability, Mg alloys are promising biodegradable implant materials for orthopedic surgeries. However, the degradation rates of Mg alloys are too fast in physiological environments, which limits the clinical applications of Mg implants. Therefore, understanding the corrosion behavior in physiological environments is crucial for developing biodegradable Mg alloys.During Mg alloy degradation, hydroxide (OH-) ions are generated, and the pH near the alloy surface increases. Since carbonate-bicarbonate (CO3 2--HCO3 -) is a vital pH buffer system in the human body, the corrosion behavior of Mg alloys would be affected by the CO2 concentrations of the test environments. In this study, we performed electrochemical and corrosion tests of a solution heat-treated WE43 (Mg-4 wt%Y-3 wt%Nd) alloy in Hanks’ balanced salt solutions (HBSS) at 37°C. By performing the tests in air and in an incubator maintained at 5% CO2, the effect of carbonate-bicarbonate pH buffering on the corrosion behavior and corrosion microstructure of the WE43 Mg alloy was investigated.When testing the WE43 Mg alloy in air, a general corrosion morphology was observed during the 24-hour immersion. In contrast, WE43 Mg alloy tested in the incubator shows a more active surface potential and localized corrosion initiates on the alloy surface in the early stages of immersion. Electrochemical impedance spectroscopy (EIS) analysis shows that WE43 Mg alloy tested in air has better corrosion resistance than in the incubator. Furthermore, the corrosion resistance of the alloy tested in air increases with immersion time but decreases when tested in the incubator. Potentiodynamic polarization curves after 24-hour immersion confirm that the corrosion current density (i corr) of the WE43 Mg alloy tested in the incubator is higher than that when tested in air. The difference in corrosion behavior is owing to the carbonate-bicarbonate pH buffering effect and will be discussed based on corrosion microstructure characterizations. Figure 1

Experimental Study on the Physical Properties of Autoclaved Bricks Made from Desert Sand and Their Resistance to Sulfate Attacks

In order to optimize the application of desert sand autoclaved bricks in rural construction in Xinjiang, this study focuses on the research and development of MU15-grade desert sand autoclaved bricks. Experimental investigations were conducted to examine the relationship between the water absorption rate of desert sand autoclaved bricks and the duration of water absorption while analyzing the impact of the water absorption rate on the compressive strength of these bricks. Additionally, experimental research was carried out to evaluate the appearance, compressive strength, and pore structure of autoclaved bricks after sulfate erosion. The results indicate the following. (1) With an increasing immersion time, the water absorption rate of desert sand-based autoclaved bricks initially rises and then declines, reaching approximately 14.74% when immersed for 4 h, which is close to the saturation water absorption rate. (2) The compressive strength of desert sand-based autoclaved bricks gradually decreases with an increasing water absorption rate, reaching its lowest point when saturation is attained, with a strength loss rate of approximately 33.18%. (3) Finally, after sulfate erosion, cracks and detachment appear on the surface of desert sand-based autoclaved bricks, and these cracks extend and propagate with the continuous accumulation of eroded products. Simultaneously, this process leads to an increase in the proportion of harmful pores by 0.96%, thereby causing a deterioration in strength. Through data analysis, a decay curve of the compressive strength erosion coefficient of desert sand-based autoclaved bricks with the number of sulfate erosion cycles was established, with good accuracy. This study provides theoretical references and technical support for the performance characteristics of desert sand-based autoclaved bricks and their application in rural construction in Xinjiang.

Performance of magnesium oxysulfate (MOS) cement prepared by MgCl2·6 H2O replacing MgSO4·7 H2O

Despite the influence of Cl- on the properties of cement-based materials, water containing Cl- is more convenient for manufacturing cement-based materials in special areas such as islands and reef construction, compared to fresh water. However, research on the effects of Cl- on the properties of magnesium oxysulfate (MOS) cement was limited. In this paper, MOS cement was prepared by replacing MgSO4·7 H2O with MgCl2·6 H2O to investigate the effect of Cl- on the evolution of MOS cement properties. The mechanical properties, water resistance, phase composition, and microstructure of MOS cement were analyzed. When the replacement rate of MgSO4·7 H2O with MgCl2·6 H2O reached 5 %, MOS cement achieved its highest compressive strength of 77.5 MPa after curing for 90 days, despite a reduction in flexural strength due to MgO hydration. After immersion in water, the trend of compressive strength change in MOS cement remained insensitive to increasing immersion time. During the curing process, Cl- facilitated the formation of hexagonal Mg(OH)2 by participating in the hydration products formation process of MOS cement. Hexagonal Mg(OH)2 contributed to matrix construction and became connected with the 5Mg(OH)2·MgSO4·7 H2O phase. Additionally, Cl- promoted the formation of the modified 5Mg(OH)2·MgSO4·7 H2O phase, known as Mg-S-O-H-Cl phase. After immersion in water, the Mg-S-O-H-Cl phase displayed stability, showcasing their capacity to maintain compressive strength relative stability despite adverse factors such as ions leaching (including Mg2+, SO42-, and Cl-) and the phase transformation of MgO.

Water-rock interfacial softening model of cemented soft rock: An experimental and numerical study

Cemented soft rock is prone to softening when exposed to water, and its mechanical properties deteriorate rapidly, which is an important reason to induce the instability and failure of engineering soft rock mass. The softening mechanism of soft rock is essentially the deterioration of microstructure caused by the change of water-rock interface. Considering the general characteristics of soft rock, the microstructural evolution characteristics and element loss over varying immersion time are then compared and analyzed. The Interfacial Cemented Bonding (ICB) structure is proposed to describe the evolution of water-rock interface. Based on the diffusion theory, the theoretical equation describing the evolution of water-rock interface is derived and compared with the experimental results. The meso-softening damage factor (MSDF) of soft rock is proposed and introduced into a numerical method to establish a strength degradation discrete element method (SD-DEM) model. The results show that the softening process of soft rock is accompanied by the shedding and suspension of particles and the dissolution of soluble substances. Besides, the softening of soft rock has obvious nonlinear dynamic characteristics. The fitting degree between the theoretical values and the experimental results is relatively high, which verifies the reliability and rationality of the dissolution-diffusion interfacial softening model. The numerical results are in good agreement with the experimental ones. This study provides a new idea for understanding the mechanism of water-induced softening characteristics and strength degradation of soft rock.