Alkaline Environment Research Articles

Reactive transport of Cd2+ in porous media in the presence of xanthate: experimental and modeling study

In mining regions, flotation reagents can interact with heavy metals, thereby increasing the complexity of their migration. However, most current studies solely focus on the migration of heavy metals, neglecting the influence of flotation reagents in their models concerning mining area pollution. This study developed the reactive transport model, Multisurface Speciation Model (MSM), which integrated the reaction processes of the three main soil components (iron oxides, organic matter, clay minerals) and ethyl xanthate (EX), a typical flotation reagent, with cadmium (Cd²⁺) to investigate the effects of EX on the transport and retention of Cd²⁺ in natural porous media under varying pH conditions. The study revealed that EX formed new adsorption sites for Cd²⁺, enhancing its retention and inhibiting transport with increased EX loading (0 to 2.5 mmol·L−1), while higher pH levels (ranging from 4 to 8) further strengthened the retention capability of Cd²⁺. The MSM further predicted the solid-phase concentration distribution of Cd²⁺ among various components. With increasing EX-loaded concentrations, xanthate became the dominant adsorbing component, accounting for 48.93% to 95.31% of adsorption, and competitively interacted with other components. Xanthate retention was lower under acidic conditions compared to neutral and alkaline environments. Sensitivity analysis highlighted the concentrations of iron oxide adsorption sites (SurfaOH, SurfbOH) as critical parameters in the models, underscoring the need for precise determination of soil physicochemical indicators. This study stressed the crucial role of flotation reagents and pH conditions in controlling heavy metal mobility, offering important insights for environmental management in mining regions.

Long-term rice cultivation enhances root development and yields by improving the structural properties of soil aggregates in saline–alkaline environments

Rice cultivation has the ability to improve saline soils. However, the effects of long-term rice cultivation on saline soil chemistry, salt ions, root characteristics, and aggregate formation remain unclear. In this study, the impact of different planting durations (1, 3, 5, 8, and 10 years) on the spatial and temporal transport of soil salts, soil chemical properties, distribution and stability of aggregates, root characteristics, and yields, were assessed. Long-term rice cultivation reduced soil pH, exchangeable sodium percentage (ESP), and EC in the 0-60cm soil layer compared to 1Y (5.45%, 61.57%, and 81.87% reduction in topsoil (0-20cm) and 8.54%, 72.82%, and 71.94 in subsoil (20-60cm), respectively). However, the soil organic matter (OM), alkaline nitrogen (AN), phosphorus (AP), and potassium (AK) increased (217.09%, 90.18%, 89.23%, and 179.18% increase in topsoil and 223.72%, 81.24%, 174.28%, and 172.57% increase in subsoil, respectively). Additionally, the Cl-, K+, and Na+ in the soil gradually leached downward with the increase in the duration of rice cultivation (55.87%、36.08%、59.80%). Simultaneously, the increased duration markedly elevated the soil macroaggregate content (11.43%-20.04% by dry-sieving and 53.48%-288.09% by wet-sieving), clayey grain content (59.17%-198.33%), and soil aggregate stability, especially for 8Y and 10Y. The improved soil structure and root characteristic under long-term rice cultivation conditions increased the yield (28.89-54.81%). Partial least squares path model displayed that rice cultivation affected the aggregate stability, root characteristics, and rice yield via the corresponding chemical properties (pH, EC, and ESP), nutrient contents (AN, AP, AK, and SOM), and salt ion contents (Cl-, K+, and Na+). These findings are critical to understanding aggregate formation in saline soils.

Study on the inhibitory behavior of high-voltage electric field on the agglomeration and sedimentation of nanoparticles in suspension

Nanoparticles can improve the heat transfer effect of fluids, however, they are difficult to dissolve in the base fluid and are prone to fouling, agglomeration and sedimentation during flow, which affects their efficient heat transfer characteristics. In this paper, the inhibitory effect of high-voltage electric field on the agglomeration and deposition of TiO2 nanoparticles in suspension was comparatively studied by comprehensive gravity sedimentation, spectrophotometer, particle size analysis, and zeta potential method. Studies have shown that the absorbance of suspensions is basically the same in neutral and acidic environments. However, in a highly alkaline environment, the agglomeration rate of nanoparticles increases significantly, resulting in a decrease in the absorbance of the suspension. The high-voltage non-uniform electric field generated by the active Cu rod electrode can effectively inhibit the agglomeration of TiO2 nanoparticles. However, the suppression effect of an external electric field is not necessarily the higher the voltage, the better. Different nanomaterials have different critical voltages. The high-voltage electric field of 1 kV has the best inhibitory effect on the agglomeration and deposition of TiO2 nanoparticles. An in-depth analysis of the mechanisms of the movement and agglomeration of TiO2 particles in suspension under high-voltage electric field excitation was conducted. The result shows that the agglomeration and sedimentation of particles in suspension depend on the Zeta potential of the nano particles. The higher the absolute value, the more stable the dispersion system is.

Impact of Acidic and Alkaline Environments on the Surface Morphology of Biodentine and White Mineral Trioxide Aggregate - An In-vitro Study.

The physical and chemical properties of calcium silicate cement might be affected due to exposure to acidic or alkaline conditions during clinical use. The present study aimed to evaluate the effect of acidic and alkaline environments on the surface morphology of biodentine (BD) and white mineral trioxide aggregate (wMTA). Disc-shaped specimens of BD (n = 30) and wMTA (n = 30) were prepared in a metal mould and wrapped in pieces of gauze. They were divided into three sub-groups according to the storage media: group A, soaked in sterile distilled water at a pH of 7.0; group B, exposed to butyric acid buffered at pH 4.0; and group C, exposed to calcium hydroxide solution buffered at pH 12.0. The specimens were incubated for 7 days at 37°C, followed by examination under scanning electron microscopy at 1000x and 5000x magnification to characterise the microstructural morphology. Definite changes were seen in the microstructure of BD and wMTA on exposure to acidic and alkaline pH. The microstructure of wMTA tends to exhibit reduced cohesion when exposed to an acidic environment, especially when compared to an alkaline pH. Acidic pH exerts a milder influence on the morphological structure of BD when contrasted with its effects on wMTA. Biodentine may emerge as a more prudent choice than wMTA for utilisation in inflamed periapical regions.

Vanadium-Doped Heterointerfaced Ni3N-MoOx Nanosheets with Optimized H and H2O Adsorption for Effective Alkaline Hydrogen Electrocatalysis.

Nickel (Ni)-based materials represent a compelling avenue as platinum alternatives in the realm of alkaline hydrogen electrocatalysis. However, conventional nickel nitrides (Ni3N) have long been hindered by sluggish hydrogen evolution kinetics in alkaline environments, owing to inadequate adsorption strengths of both hydrogen and water molecules. Herein, a novel approach is presented involving the design of vanadium (V)-doped Ni3N/MoOx heterogeneous nanosheets (V-Ni3N@MoOx), engineered to achieve optimized adsorption strengths for hydrogen evolution and oxidation reactions (HER/HOR). Theoretical insights underscore the superior catalytic performance of this composite, attributed to a synergistic interplay between unique V doping and the heterointerfaced structure. This synergistic effect not only fine-tunes the electronic structure, establishing an optimal d band center to mitigate proton over-bonding, but also ameliorates the energy barrier through enhanced H2O dissociation capability. Consequently, V-Ni3N@MoOx manifests remarkable catalytic activities, evincing an overpotential of 56mV at 10mAcm-2 for HER and an exchange current density of 1.91mAcm-2 for HOR in alkaline media. Notably, the stability assessment reveals the enduring performance of V-Ni3N@MoOx for HER/HOR, exhibiting no activity decay over extended operational durations. This study underscores the efficacy of heterogeneous interface modulation as a transformative strategy in designing Ni-based materials for alkaline hydrogen electrocatalysis.

Self-cleaning electrode for stable synthesis of alkaline-earth metal peroxides.

Alkaline-earth metal peroxides (MO2, M = Ca, Sr, Ba) represent a category of versatile and clean solid oxidizers, while the synthesis process usually consumes excessive hydrogen peroxide (H2O2). Here we discover that H2O2 synthesized via two-electron electrochemical oxygen reduction (2e- ORR) on the electrode surface can be efficiently and durably consumed to produce high-purity MO2 in an alkaline environment. The crucial factor lies in the in-time detachment of in situ-generated MO2 from the self-cleaning electrode, where the solid products spontaneously detach from the electrode to solve the block issue. The self-cleaning electrode is achieved by constructing micro-/nanostructure of a highly active catalyst with appropriate surface modification. In experiments, an unprecedented accumulated selectivity (~99%) and durability (>1,000 h, 50 mA cm-2) are achieved for electrochemical synthesis of MO2. Moreover, the comparability of CaO2 and H2O2 for tetracycline degradation with hydrodynamic cavitation is validated in terms of their close efficacies (degradation efficiency of 87.9% and 93.6% for H2O2 and CaO2, respectively).

Prussian Blue-Derived Atomic Fe/Fe3C@N-Doped C Catalysts Supported by Carbon Cloth as Integrated Air Cathode for Flexible Zn-Air Batteries.

The development of an integrated air cathode with superior oxygen reduction reaction (ORR) performance is fundamental to flexible zinc-air batteries (ZABs) for wearable electronics. Herein, a self-assembled metal-organic framework (MOF)-derived strategy is proposed to prepare a atomic Fe/Fe3C@N-doped C catalysts supported by carbon cloth (CC) catalyst for use as an air cathode of flexible ZABs. The Prussian Blue precursor, which self-assembles on the surface of the carbon cloth due to electrostatic attraction, is critical in achieving the uniform dispersion of catalysts with high density loading on carbon cloth substrates. The hollow cubic structure, N-doped carbon layer coating, and the integrated electrode design can provide more accessible active sites and facilitate a rapid electron transfer and mass transport. Density functional theory (DFT) calculation reveals that the electronic interactions between the Fe-N4 and Fe3C dual active sites can optimize the adsorption-desorption behavior of oxygen intermediates formed during the ORR. Consequently, the Fe/Fe3C@N-doped C/CC exhibits an excellent half wave potential (E1/2 = 0.903V) and superior long-term cycling stability in alkaline environments. With excellent ORR performance, ZABs and flexible ZABs based on Fe/Fe3C@N-doped C/CC air cathode demonstrate excellent overall electrochemical performance in terms of open circuit voltage, maximum power density, flexibility, and cycling stability.

Chemical Constituents from the Whole Plants of Limonium sinense and Their in vitro Anti-inflammatory Activity.

The Yellow River Delta possesses lots of characteristic medicinal plants due to its high salinity and high alkaline environment and Limonium sinense is an iconic plant. However, there are very few studies on L. sinense and its chemical constituents have not been investigated in recent ten years. In the present study, the chemical constituents and bioactivities of L. sinense were fully studied for the first time. UPLC-MS/MS method combined with database comparison identified 109 compounds mainly including flavonoids, alkaloids and polyphenols. In addition, the potential bioactivities of L. sinense were considerated as anti-inflammatory, anti-oxidative, anti-tumor, hepatoprotective and hpyerglycemic activities based on these identified compounds and their related literature. Furthermore, four derivatives of 12-oxo-phytodienoic acid and butenolide including two new ones (1 and 2) were isolated from the whole plants of L. sinense. Their structures, including the absolute configurations, were determined by the analysis of comprehensive spectroscopic data. All isolates were evaluated for their anti-inflammatory activity. Compound 1 exhibited moderate anti-inflammatory activity with IC50 value of 37.5±1.2 μM on NO production level.

Bifunctional SnO2/NiO/rGO nanocomposite electrode for hydrogen evolution reaction and detection of winter wheat cold-resistant RNA.

Aconvenient, non-toxic, and low-cost tin dioxide (SnO2)/nickel oxide (NiO)/reduced graphene oxide (rGO) nanocatalytic electrode was investigated, which can effectively promote the hydrogen evolution reaction and can also be used to construct a sensitive winter wheat cold-tolerant RNA sensor. Due to the good synergy and photocurrent generation between SnO2 and NiO, which accelerates the electron transfer and catalyzes the hydrolysis reaction, the resultant data for the hydrogen evolution reaction in alkaline environment of this material are very impressive, with cathodic current densities of up to 10mAcm-2. The marvelous heterostructures and photovoltaic properties form a signal amplification system, which enables the nanocomposites to have an excellent linear sensitivity in low-concentration RNA solutions. The single-stranded complementary RNA of the target RNA was immobilized on the surface of the nanocomposites, which enabled the materials to recognize the target RNA under enzyme-free conditions. The test results showed that the modified electrode materials had good single detection performance in a wide linear range from 0.1nM to 2mM, with the limit of detection (LOD) of 0.078nM. The developed nanocomposite electrode has good performance in hydrogen evolution and winter wheat cold-resistant RNA detection, and is a bifunctional device with superior performance.

Mechanical properties and chemical microscopic characteristics of all-solid-waste composite cementitious materials prepared from phosphogypsum and granulated blast furnace slag

Industrial wastes, such as phosphogypsum, are characterized by high production and accumulation volumes, and significant pollution. A high-performance, all-solid waste, phosphogypsum-based composite cementitious material (PCCM) was developed by using a hybrid ball milling method and thermal activation to stimulate various industrial wastes. Optimization of rationing was analyzed using extreme variance, standard variance, and multiple regression models. The macro-engineering parameters of PCCM were evaluated through flexural and compressive tests. The mineralogical composition, functional groups, micro-morphology, and molecular structure of PCCM were examined through micro-testing. When the mass ratio of Ball milled calcined phosphogypsum (BCPG) to granulated blast furnace slag (GGBS) is 1.2:1, with a 4 % addition of calcium oxide and a water-cement ratio of 0.4, the 28-day flexural and compressive strengths, as well as the softening coefficients, of PCCM can reach 7.27 MPa, 40.1 MPa, and 0.922, respectively, closely matching the performance of C42.5 cement. Under the synergistic effects of the hydration reaction and an alkaline environment, the CaSO4 in the PCCM system hydrated and crystallized to produce gypsum-phase crystals, enhancing early strength properties by 60–174 %. As hydration continued, SO42- reacted with silicon and aluminum oxides, prompting secondary hydration of GGBS, and increasing AFt and C-(A)-S-H in the system. This research offers a new approach for the co-disposal and resource utilization of various solid wastes while identifying a cementitious material that can replace traditional cement in practical engineering applications.

Hydroxy-Carboxylic Acids as Green and Abundant Ligands for Sustainable Recovery of Copper from a Multimetallic Powder: A Proof of Concept.

The recovery of copper and other valuable metals had become increasingly strategic for the future of the global economy, particularly in regions lacking abundant mineral resources, such as most European countries. In this study, we investigated the viability of utilizing environmentally friendly, cost-effective, abundant and bio-based ligands, specifically carboxylic acids and their derivatives, for copper leaching in a low-temperature hydrometallurgical process. Our investigation focused on elucidating the impact of substituents in the α position of hydroxy-carboxylic acids on copper solubilization efficacy. Notably, hydroxy-carboxylic acids, like malic acid and lactic acid, were evidenced as particularly promising ligands for leaching copper from a custom-made multimetallic powder. By thoroughly characterizing the obtained complexes (Raman, UV-Vis) and by supporting the experimental efforts by a Design of Experiment (DoE) approach, we optimized the leaching process. The influence of experimental parameters such as pH, temperature, leaching time, and Cu/ligand molar ratio on process yield (determined through Inductively Coupled Plasma - Optical Emission Spectroscopy, ICP-OES, analysis) was thoroughly investigated. Additionally, we developed a subsequent copper recovery step by precipitating copper (II) hydroxide in an alkaline environment, guided by speciation diagrams tailored for each copper-ligand system.

Catalytic Degradation of Bisphenol A in Water by Non-Thermal Plasma Coupled with Persulfate

Bisphenol A (BPA) has become prevalent in the environment due to its extensive use in industrial materials, thus raising significant concerns regarding its potential toxicity and health effects. In this study, an efficient and eco-friendly non-thermal plasma (NTP) was used to catalyze persulfate (PS) for BPA decomposition, and the results showed that the integrated system could effectively degrade BPA. The best performance was attained at a PS to BPA mass ratio of 5:1, with a degradation rate of 91.3% following a 30 min treatment. The degradation rate of BPA increased with increasing input voltage and frequency; conversely, it decreased with an increase in BPA’s initial concentration. Higher BPA degradation rates could be achieved in alkaline environments. Radical quenching experiments revealed that SO4−•, OH•, O2−• and 1O2 were important active substances involved in BPA degradation. Nine intermediate products were identified by liquid chromatography–mass spectrometry (LC-MS), and four degradation pathways were deduced. Additionally, a toxicity analysis of intermediate products was performed. The significant decrease in chemical oxygen demand (COD) during the actual wastewater treatment suggested that the NTP/PS system has good applicability in actual wastewater treatment.

Purple urine bag syndrome: a unique clinical case and management considerations

Purple urine bag syndrome (PUBS) is a rare and unusual event. It is related to symptomatic urinary infection and asymptomatic bacteriuria in patients with indwelling bladder catheters. The purple color of the urine is due to metabolic products of biochemical reactions formed by bacterial enzymes in the urine. Gastrointestinal tract flora breaks down the amino acid tryptophan into indole, which is subsequently absorbed into the portal circulation and converted into indoxyl sulfate. Indoxyl sulfate is then excreted into the urine, where it can be broken down into indoxyl if the appropriate alkaline environment and bacterial enzymes are present. The breakdown products, indigo, and indirubin appear blue and red. We reported on an elderly woman who was kept in a nursing home, had multiple comorbidities such as history of cerebrovascular accident (CVA), acute kidney injury (AKI) and she was hospitalized due to decreased consciousness, fever and kidney failure. On the third day of hospitalization, the patient developed PUBS while undergoing urinary catheterization in the hospital. She had no history of previous catheterization and chronic use of antibiotics, she was only using Tolterodine for a long time due to urinary urgency. Due to antibiotic resistance, the drugs were not changed and the purple color disappeared after changing the catheter and urinary bag.This was the first patient in this region to be reported with this manifestation.

Interface Engineering Induced by Low Ru Doping in Ni/Co@NC Derived from Ni-ZIF-67 for Enhanced Electrocatalytic Overall Water Splitting.

Electrochemical water splitting is a promising approach for hydrogen evolution reactions (HER); however, the oxygen evolution reaction (OER) remains a major bottleneck due to its high energy requirements. High-performance electrocatalysts capable of facilitating HER, OER, and overall water splitting (OWS) are highly needed to improve OER kinetics. In this work, we synthesized a trimetallic heterostructure of Ru, Ni, and Co incorporated into N-doped carbon (denoted as Ru/Ni/Co@NC) by first synthesizing Ni/Co@NC from Ni-ZIF-67 polyhedrons via high-temperature carbonization, followed by Ru doping using the galvanic replacement method. Benefiting from increased active surface sites, modulated electronic structure, and enhanced interfacial synergistic effects, Ru/Ni/Co@NC exhibited exceptional electrocatalytic performance for both HER and OER processes. The optimized Ru/Ni/Co@NC catalyst, with a minimal Ru mass ratio of ∼2.07%, demonstrated significantly low overpotential values of 34 mV for HER and 174 mV for OER at a current density of 10 mA/cm2 with corresponding Tafel slope values of 33.42 and 34.39 mV/dec, respectively. Further, the optimized catalyst was loaded onto carbon paper and used as anode and cathode materials for alkaline water splitting. Interestingly, a low cell voltage of just 1.44 V was obtained. The enhanced electrolytic performance was further elaborated by density functional theory (DFT) calculations, which confirmed that Ru doping in Ni/Co introduced additional active sites for H*, enhancing adsorption/desorption abilities for HER (ΔGH* = -0.30 eV), lowering water dissociation barrier (ΔGb = 0.49 eV) and reducing the energy barrier for the rate-determining step of OER (O* → OOH*) to 1.62 eV in an alkaline environment. These findings reflect the significant potential of ZIF-67-based catalysts in energy conversion and storage applications.

The Ways of Forming and the Erosion/Decay/Aging of Bioapatites in the Context of the Reversibility of Apatites

This study primarily focused on the acid erosion of enamel and dentin. A detailed examination of the X-ray diffraction data proves that the products of the acid-caused decay of enamel belong to the family of isomorphic bioapatites, especially calcium-deficient hydroxyapatites. They are on a trajectory towards less and less crystallized substances. The increase in Bragg’s parameter d and the decrease in the energy necessary for the changes were coupled with variability in the pH. This was valid for the corrosive action of acid solutions with a pH greater than 3.5. When the processes of natural tooth aging were studied by X-ray diffraction, a clear similarity to the processes of the erosion of teeth was revealed. Scarce data on osteoporotic bones seemed to confirm the conclusions derived for teeth. The data concerning the bioapatite decays were confronted with the cycles of apatite synthesis/decay. The chemical studies, mainly concerning the Ca/P ratio in relation to the pH range of durability of popular compounds engaged in the synthesis/decay of apatites, suggested that the process of the formation of erosion under the influence of acids was much inverted in relation to the process of the formation of apatites, starting from brushite up to apatite, in an alkaline environment. Our simulations showed the shift between the family of bioapatites versus the family of apatites concerning the pH of the reaction environment. The detailed model stoichiometric equations associated with the particular stages of relevant processes were derived. The synthesis processes were alkalization reactions coupled with dehydration. The erosion processes were acid hydrolysis reactions. Formally, the alkalization of the environment during apatite synthesis is presented by introducing Ca(OH)2 to stoichiometric equations.

ნიადაგით გამოწვეული ელექტროქიმიური კოროზია ტენიან, ნაკლებ მჟავიან, ნეიტრალურ და ტუტოვან გარემოში

The article analyzes the anodic, transient and cathodic processes of a galvanic cell. Electrochemical corrosion caused by soil in a moist, less acidic, neutral and alkaline environment is discussed. The scheme of corrosion of underground pipelines under various conditions of soil aeration is given. The cases of corrosion process control for various soil corrosion conditions are considered: soil corrosion with prevailing cathodic control; corrosion in loose, dry soils (anodic control); corrosion over long stretches (prevailing ohmic control).

Innovative thermal crosslinked polyimide gas separation membrane with highly selective and resistance to physical aging base on phenyl ethynyl

In this study, a high performance phenyl ethynyl thermal crosslinked 6FDA-based polyimide (CR-4ETA-x) was developed, which has high gas permeability and selectivity, resistance to physical aging. By introducing 4,4′-(Acetylene-1,2-diyl) diphthalic anhydride (4ETA) monomer into the polyimide structure, the thermal crosslinking precursor membrane was formed. The precursor membrane was heat treated at 440℃ to obtain CR-4ETA-x. After heat treatment, we detected the olefin radical in the crosslinked membrane by electron paramagnetic resonance, which proved that the polyimide network was formed. This allows the crosslinked membrane to have greater d-spacing, higher rigidity, and BET surface area. The CO2 permeability of CR-4ETA-5% is 4114 barrer and the CO2/CH4 selectivity is 19.22. Compared to 6FDA-DAM, the CO2 permeability increased by 477% while the selectivity decreased by only 17%. CR-4ETA-20% shows the CO2 permeability of 3560 Barrer and CO2/CH4 selectivity of 21.1 in CO2/CH4 mixed-gas. After 60 days of aging the permeability maintenance of CR-4ETA-20% were 88%, 84%, 83% and 91% for O2, N2, CO2 and CH4. In addition, in the long-term stability test of more than 100 h, the separation performance of CR-4ETA-20% did not decrease significantly. However, CR-4ETA-x also has limitations, such as poor stability in alkaline environments and lower gas permeability than some advanced carbon molecular sieve membranes. In general, the method of phenyl ethynyl thermal crosslinking provides an effective way for the development of CO2 separation membranes with possible applications.

Fracture toughness of alkali-activated concrete subjected to aggressive environment

This study investigates the fracture toughness of alkali-activated granulated blast-furnace slag (GBFS)-based geopolymer concrete (GPC), non-activated slag cement concrete, and ordinary Portland cement (OPC) concrete in acidic, alkaline, and chloride solutions over six months. A total of 580 centrally straight-notched Brazilian disc (CSNBD) specimens were cast to assess pure mode-I (0°), pure mode-II (28.7°), and mixed-mode (15° and 45°) fractures under these conditions. Microstructural analyses (SEM) were performed to evaluate microstructural changes after six months of exposure. Results showed that GPC exhibited the lowest initial fracture toughness but the smallest reduction (7 %-11 % depending on the mode) across all environments, with slag cement concrete and OPC experiencing reductions of 11 %-14 % and 14 %-21 %, respectively, in acidic conditions. In alkaline environments, GPC showed a 3 %-6 % decrease in fracture toughness, while OPC and slag cement concrete showed reductions of 6 %-13 %. The gradient boosting regressor accurately predicted the failure load of CSNBD specimens, achieving an R² score of 0.948. Finally, SHAP sensitivity analysis identified concrete type, exposure time, and environment as critical input features, consistent with experimental results.

Surface modification of fibres with silane for enhancing the durability of FRP composites as reinforcement for seawater sea sand concrete (SWSSC): A review

This review discusses the necessity of surface modification to effectively use fibre-reinforced polymers (FRPs) as reinforcements for seawater and sea sand concrete (SWSSC). FRPs can be a viable reinforcement material for SWSSC as an alternative to the traditional carbon steel reinforcement that will suffer unacceptably high rates of corrosion due to the very high chloride content of the SWSSC environment. FRPs exhibit mechanical properties similar to steels but suffer insignificant degradation/corrosion due to chloride. However, the fibres in certain FRPs (such as basalt FRPs and glass FRPs) suffer degradation due to attack by the alkaline environment of concrete, causing degradation in fibre-matrix interfacial strength and loss of FRPs’s overall mechanical strength and durability. Therefore, fibres used in such FRPs require suitable surface modification to ameliorate their degradation, enabling their practical use as reinforcements of SWSSC. While carbon fibre-reinforced polymers (CFRPs) demonstrate superior resistance to alkali-induced degradation, their widespread use in large-scale civil engineering is hindered by high costs. In this review, more economic alternatives, i.e., basalt fibre-reinforced polymers (BFRPs) and glass fibre-reinforced polymers (GFRPs) are critically reviewed. To enhance the durability of FRPs and mitigate alkali-induced degradation of the basalt/glass fibres, suitable surface modifications are necessary to safeguard the mechanical properties of FRPs. Underpinned by a comprehensive discussion on the necessity of surface modification of fibres for the use of FRPs in SWSSC environment, this review focuses on the potential of advanced approaches for surface modifications of the fibres, i.e., coatings of silanes, and silanes impregnated with graphene nanoplatelets (GNPs), graphene oxide (GO) and its functionalised derivatives or metal oxides (such as SiO2, ZrO2, Al2O3, TiO2 and CeO2). This review critically discusses the opportunities for suitable surface modification of basalt and glass fibres for enabling the durable use of FRPs as reinforcements for sweater sea sand concrete.

Investigation into the long-term alkali resistance of basalt fibers

To more accurately simulate the alkaline environment of basalt fiber in cement-based materials, this study innovatively employs the benchmark cement supernatant as the alkaline solution for the long-term corrosion testing of basalt fiber (BF). Additionally, through mechanical performance testing of mortar containing basalt fiber at different ages, the study reveals the corrosion behavior of basalt fiber in an alkaline environment. The results indicate that basalt fiber undergoes corrosion in the benchmark cement supernatant, where the OH− ions in the solution react with SiO2 in the basalt fibers, thereby disrupting the silicate framework of the fibers and causing pitting corrosion on the fiber surface. The black and white binarization analysis of the SEM images of BF7 after 360d erosion revealed that the corrosion pits covered 31.50 % of the fiber surface area, indicating severe corrosion. Furthermore, the study on the long-term mechanical properties of basalt fiber mortar demonstrated an initial increase in performance, followed by a gradual decline as the curing age progressed. Notably, after 360d of curing, the flexural strength of basalt fiber mortar was lower than that at 30d. For instance, the 360d flexural strength of BF1-0.1 and BF7-0.1 decreased by 18.85 % and 14.54 %, respectively, compared to 30d. This decline is primarily attributed to the corrosion of basalt fibers in alkaline environments, leading to a decrease in their mechanical properties. Therefore, it is essential to enhance the alkali resistance of basalt fibers when used in cement-based materials.