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Table of Content

    Volume 45 Issue 7
    15 July 2026
  • Cement and Concrete
    Chemical Shrinkage Characteristics of Supersulfated Cement
    ZHANG Xuemei, JIN Qingqing, CHANG Shuo, WANG Lu, LI Zhaoqi, ZHANG Xingzhao, LIU Shuhua
    2026, 45(7):  2215-2225.  doi:10.16552/j.cnki.issn1001-1625.2025.1297
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    Volume deformation caused by chemical shrinkage readily leads to material cracking, compromising structural integrity. As a novel low-carbon cementitious material, supersulfated cement exhibits significant differences in its hydration process and chemical shrinkage characteristics compared to traditional Portland cement. This study employed granulated blast furnace slag, phosphogypsum and cement clinker to prepare phosphogypsum-based supersulfated cement (SSC), investigating the effects of phosphogypsum modification, phosphogypsum content, clinker content and water-binder ratio on SSC chemical shrinkage. The influence mechanisms were explored through microscopic testing characterisation. The results indicate that the chemical shrinkage value of SSC is approximately 0.046 mL/g at 7 d, accounting for roughly 77% of ordinary Portland cement (OPC). Calcined phosphogypsum-based supersulfated cement (CSSC) exhibits a 17.39% reduction in chemical shrinkage value compared to SSC, while lime-neutralized phosphogypsum-based supersulfated cement (NSSC) shows the 65.21% increase in chemical shrinkage value relative to SSC. With increasing phosphogypsum content, the chemical shrinkage of SSC increases, reaching its minimum at 13% (mass fraction, the same below) phosphogypsum content. As the clinker content increases, the chemical shrinkage value of SSC initially decreases and then increases. The chemical shrinkage value is minimal at a 5% (mass fraction) clinker content. For SSC, chemical shrinkage value decreases with increasing water-binder ratio. The synergistic effect of 15% phosphogypsum and 5% clinker achieves optimal matching between ettringite formation and calcium silicate hydrate (C-S-H) gel structure, thereby attaining the optimum value for chemical shrinkage control.

    Influence of Oleic Acid Modified Ultrafine Cement on Performance of Grouting Materials
    CAO Yujie, LIU Lv, HUANG Dong, HUANG Chaoqun, LIU Yunpeng
    2026, 45(7):  2226-2236.  doi:10.16552/j.cnki.issn1001-1625.2026.0054
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    In the repair of concrete micro-cracks, ultrafine cement (UPC) faces the problems of poor slurry fluidity, high porosity and susceptibility to dissolution under low water-cement ratio. In this study, the surface modification of UPC with oleic acid was proposed to simultaneously improve its injectability and hydrophobicity. Oleic acid modified UPC with oleic acid content of 0%~0.3% (mass fraction) was prepared by ball milling method. The rheological properties, compressive strength, heat of hydration, hydrophobic properties and interfacial bond strength of the modified UPC paste were systematically evaluated, and the modification mechanism was revealed by FTIR, SEM, TG, LF-NMR. The results show that appropriate amount of oleic acid (0.1%) modification can reduce the viscosity of grouting material and improve the rheological properties. At the same time, at this dosage, the inhibition effect on cement hydration is small, the strength of the slurry is not much affected, and the autogenous shrinkage of the slurry is significantly reduced. Oleic acid is involved in the surface modification of cement particles, and the contact angle of hardened slurry increases from 48.6° to 126.4°. However, an excessive amount of oleic acid (>0.2%) severely inhibits the hydration reaction, reduces the 28 d compressive strength from 54.95 MPa to 23.08 MPa, and increases the autogenous shrinkage and porosity. In this paper, the study investigates the action mechanism and dosage threshold of oleic acid in UPC, which provides support for the development of high-performance microfracture anti-seepage repair materials.

    Effects of Red Mud-Based Composite Hydration Seeds on Properties of Portland Cement Mortar
    LI Fuyun, HUANG Shengjing, JIAO Weili, DENG Xiaowei, CHEN Chunheng, WEI Chi, LAI Fang, LI Jing
    2026, 45(7):  2237-2249.  doi:10.16552/j.cnki.issn1001-1625.2025.1317
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    To enhance the efficient resource utilization of red mud in cement-based materials, this study prepared red mud-based composite hydration seeds (RM-CAW) via acid leaching pretreatment combined with hydrothermal synthesis, and incorporated them into cement mortar to systematically investigate their effects on cement hydration behavior, microstructure, and mechanical properties. Mechanical performance tests together with X-ray diffraction(XRD), thermogravimetric analysis(TG), scanning electron microscopy(SEM), and specific surface area and pore size distribution analyses were conducted to elucidate the strengthening mechanism of RM-CAW. The results indicate that the incorporation of RM-CAW significantly improves the mechanical properties of cement mortar at both 7 and 28 d. In particular, compared with reference cement mortar, the mortar with 5.0%(mass fraction) RM-CAW (HARM-5.0) specimen exhibits increases of 11.1% and 6.9% in flexural strength and compressive strength at 28 d, respectively. The addition of RM-CAW promotes the formation of hydration products such as calcium silicate hydrate(C-S-H), has a pronounced improvement in the interfacial transition zone and an overall densification of the matrix, and promotes pore structure refinement and a reduction in the proportion of large pores.

    Durability Analysis of Steel Fiber Reinforced Concrete under Coupled Salt Freeze-Thaw and Dry-Wet Cycles
    MA Yue, ZHANG Bo, WU Shoujun, LIU Yanyu, LIU Biao, HE Wei
    2026, 45(7):  2250-2259.  doi:10.16552/j.cnki.issn1001-1625.2026.0059
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    Concrete structures in cold marine regions are exposed to chloride attack, freeze-thaw action, and alternating wetting and drying. The combined effects of these processes promote internal damage accumulation and compromise long-term structural safety. Steel fibers can bridge cracks and restrict their propagation, thereby improving concrete resistance to environmental attack. However, the durability and flexural toughness evolution of steel fiber-reinforced concrete (SFRC) under the coupled effects of chloride attack, freeze-thaw cycling, and dry-wet cycling remain insufficiently understood. To address this gap, this study adopted a staged coupling regime reflecting the seasonal conditions of cold marine environments and investigated the macroscopic deterioration and microscopic damage mechanisms of SFRC.

    Laboratory accelerated tests were conducted on C40 ordinary concrete (NC) and SFRC containing approximately 2% (volume fraction) corrugated steel fibers. A 3.5% (mass fraction) NaCl solution was used to simulate the chloride environment of seawater. Two exposure regimes were designed: salt freeze-thaw cycling alone and a coupled regime that combined salt freeze-thaw with dry-wet cycling. In the coupled regime, 50 salt freeze-thaw cycles were first applied to simulate cumulative winter freeze-thaw damage, followed by seven dry-wet cycles to represent alternating wetting and drying in tidal or splash zones during the non-freezing season. This sequence constituted one coupled cycle. The mass loss rate, relative dynamic modulus of elasticity, flexural strength, load-displacement response, and flexural toughness were evaluated. Scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS) were used to characterize deterioration of the cementitious matrix and changes in the interfacial transition zone between the steel fibers and cementitious matrix.

    The results show that coupled salt freeze-thaw and dry-wet cycling markedly accelerate concrete deterioration. After four coupled cycles, the relative dynamic modulus of elasticity of NC falls below 60%, while the flexural strengths of NC and SFRC decrease by 33.3% and 29.5%, respectively. The smaller reduction in SFRC demonstrates that steel fibers enhance concrete durability under the coupled environment. Nevertheless, the flexural toughness of SFRC progressively decreases with cycling. After four coupled cycles, its peak load decreases by 27.6%, and the characteristic double-peak response tends to disappear, indicating a continuing loss of fiber-bridging and energy-dissipation capacity.

    Microstructural observations indicate that frost-induced expansion and drying shrinkage jointly promote crack propagation and increase pore connectivity. As a result, Cl- ingress is accelerated. Chloride-bearing reaction products, including Friedel’s salt, accumulate in pores and cracks; their expansion generates additional stresses and induces further microcracking. Chloride-induced corrosion roughens the steel-fiber surface, damages the interfacial transition zone, weakens fiber-matrix bonding and consequently reduces frictional energy dissipation during fiber pullout. These processes create a self-reinforcing sequence of crack propagation, ion diffusion, chemical attack, accumulation of expansive products, and renewed crack growth, which is identified as the primary mechanism driving the rapid degradation of the physical and mechanical properties of concrete. By linking macroscopic performance loss with microstructural evidence at the matrix and interface scales, this study clarifies the coupled deterioration mechanism of SFRC and demonstrates that flexural toughness is particularly sensitive to environmental damage. The findings provide a scientific basis for durability design, in-service condition assessment, and service-life prediction of SFRC structures in cold marine environments.

    Experimental Study on Bond Performance Between Steel-PVA Hybrid Fiber Reinforced Concrete and Steel Bars under Freeze-Thaw Cycles
    XU Chengxiang, WANG Rui, XU Qiqi, YANG Zhao
    2026, 45(7):  2260-2274.  doi:10.16552/j.cnki.issn1001-1625.2025.1263
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    In order to investigate the bond performance between steel-polyvinyl alcohol hybrid fiber reinforced concrete (S-PVA HFRC) and steel bars under freeze-thaw cycles, 75 S-PVA HFRC specimens were designed and fabricated based on orthogonal test factors, namely steel fiber volume fraction, PVA fiber volume fraction, and mineral powder replacement rate. These specimens were subjected to freeze-thaw cycles with different numbers of cycles, followed by central pull-out tests under monotonic loading. The failure modes, bond strength, interfacial bond stiffness and toughness of S-PVA HFRC specimens under different test parameters were studied, and the influence of each parameter on the bond-slip mechanical behavior of S-PVA HFRC under freeze-thaw conditions was analyzed. The results show that all S-PVA HFRC specimens exhibit steel bar pull-out failure; the bond strength of S-PVA HFRC specimens decreases with the increase in the number of freeze-thaw cycles. After an identical number of freeze-thaw cycles, the bond strength and peak slip of S-PVA HFRC specimens are higher than those of fiber-free plain concrete specimens. After 50 freeze-thaw cycles, the bond strength of S-PVA HFRC specimens exhibit the most significant enhancement. Compared with fiber-free plain concrete specimens, the S-PVA HFRC specimens exhibit the greatest increase of 53.75% when the volume fraction of steel fiber is 1.3%, the volume fraction of PVA fiber is 0.2%, and the replacement rate of mineral powder is 15% (mass fraction). The incorporation of hybrid fibers effectively mitigates the adverse effect of freeze-thaw damage on the interfacial bond stiffness and significantly improves the energy dissipation capacity of the specimens. A bond-slip model for the interface between S-PVA HFRC and steel bars under freeze-thaw conditions is proposed, which shows good agreement with the experimental results.

    Effects of Spalling Area and Interfacial Shear Stress on Fiber Pullout Behavior in Ultra-High Performance Concrete
    XIANG Gucong, NIU Yanfei, LIN Xihua, YUAN Zong, GUO Yanlong, YUAN Lijun
    2026, 45(7):  2275-2289.  doi:10.16552/j.cnki.issn1001-1625.2025.1236
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    To investigate the influence of the spalling zone and interfacial shear stress on the pullout behavior of steel fibers in ultra-high performance concrete (UHPC), the pullout behavior of steel fibers at different curing ages (7, 14, 28 d) and embedment angles (0°, 30°, 45°, 60°) was studied. The degree of matrix spalling was evaluated, and the pullout behavior was analyzed using a micromechanical model. The results show that the pullout load and average bond strength are maximized at 45° for different embedment angles, while the maximum pullout energy occurrs at 60°. The spalling area of the matrix is less affected by the curing age but significantly influenced by the embedment angle, with the maximum spalling area occurring at 60°. An equation is established to describe the relationship between the spalling area and the embedment angle. The degradation of interfacial shear stress determines the trend of the descending branch (debonding stage), with the shape changing from concave to convex and the curvature of the convex shape gradually increasing with different curing ages and embedment angles. Extending the value of shape coefficient η from 0.10 to -0.05 and introducing an interfacial enhancement factor b with a range of values from -8 to -2 can effectively evaluate the change of the interfacial shear stress, the results of the numerical analysis are in good agreement with experimental results.

    Sulfate Erosion Resistance of Composite Alkali-Reducing Modified Ecological Porous Concrete
    OUYANG Qi, YIN Jian, LI Sijiao, CHEN Yihao, QIN Yuhang, ZENG Yi
    2026, 45(7):  2290-2298.  doi:10.16552/j.cnki.issn1001-1625.2025.1298
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    In order to improve the service durability of ecological porous concrete (EPC) in a sulfate dry-wet cycling environment, a composite alkali-reduction system was established using diatomaceous earth (DE), oxalic acid (OA) and ferric sulfate (FS). EPC specimens with different alkalinity gradients were prepared, and the evolution of macroscopic property and the variation of microstructure under sulfate dry-wet cycles were systematically investigated. The macroscopic deterioration behavior of EPC was characterized by relative compressive strength and mass loss rate, while hydration products and microstructural features were analyzed by XRD, FTIR, and SEM. The results show that moderate alkali reduction significantly improves the sulfate erosion resistance of EPC. Among the specimens, the group with 1.2% (mass fraction) OA-FS composite system (pH=9.0 to 10.0) still maintains the highest relative compressive strength (72.59%) after 24 sulfate dry-wet cycles. Microstructural characterization shows that the DE-OA-FS composite system optimizes the pore structure and chemical stability of EPC by promoting the formation and structural stabilization of C-S-H gel, slowing the rapid consumption of Ca(OH)2, and inhibiting the concentrated precipitation of sulfate-attack products such as ettringite (AFt), thereby delaying the process of crack propagation and carbonation-induced deterioration. The findings provide a technical reference for durability optimization design and engineering applications of EPC in complex aggressive environments.

    Damage Law and Life Prediction of CO2 Curing Biochar Recycled Concrete under Salt Freezing Environment
    WANG Mengyao, ZHAO Yuanzhuo, DU Wenfeng, HE Zhongying
    2026, 45(7):  2299-2311.  doi:10.16552/j.cnki.issn1001-1625.2025.1257
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    To enhance the durability of recycled concrete in cold saline-alkaline regions, this study focused on C30 recycled concrete with five biochar incorporation levels (0%,2.0%,4.0%,6.0%, and 8.0%,mass fraction). Two curing methods,standard curing and CO2 curing,were applied. Sulfate freeze-thaw cycle tests were conducted to measure macroscopic indicators including mass loss rate, relative dynamic elastic modulus, and compressive strength loss rate. Microscopic pore structure analysis was performed using nuclear magnetic resonance (NMR) technology. A damage model based on the Weibull distribution was established to predict service life of concrete under salt freezing environment. The results show that biochar significantly improves the salt-freeze resistance of recycled concrete, with an optimal incorporation rate being 4.0%. After 300 freeze-thaw cycles under standard curing, the mass loss rate, relative dynamic elastic modulus, and compressive strength loss rate of the 4.0% biochar group improve by 46.8%, 58.0%, and 22.7%, respectively, compared with the reference group. CO2 curing further enhances the performance, reducing the mass loss rate and compressive strength loss rate by 36.8% and 33.1%, respectively, compared with the standard-cured group at the same biochar content. The porous adsorption characteristics of biochar, combined with the densification effect of CO2 curing through carbonation, synergistically optimize the pore structure and reduce the proportion of harmful pores. The damage model based on the Weibull distribution exhibits a good fit and predicte that the service life of the optimal combination (4.0% biochar with CO2 curing) in North China could reach 9 288 d, which is 175.4% longer than that of the reference group. The study confirms that the synergistic effect of biochar and CO2 curing produces a “1+1>2” enhancement effect on the salt-freeze resistance of recycled concrete, significantly extending its service life in cold saline-alkaline environments.

    Effects of Resonant Aggregate Characteristics on Blast Mitigation and Vibration Suppression Performance of Metaconcrete
    FU Youyun, CHEN Zhihua, HE Feng, LIU Gang
    2026, 45(7):  2312-2323.  doi:10.16552/j.cnki.issn1001-1625.2025.1193
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    To investigate the vibration suppression performance of metaconcrete under blast loading, a three-dimensional finite element model of metaconcrete measuring 100 cm×100 cm×30 cm was established based on the theory of locally resonant metamaterials. The Arbitrary Lagrangian-Eulerian (ALE) method was employed to simulate TNT blast loading, and the effects of material properties, geometric dimensions, and non-uniform distribution of resonant aggregates on the vibration suppression performance of metaconcrete were systematically analyzed. The results show that metaconcrete can effectively attenuate blast-induced stress waves through local resonance. Within the parameter ranges studied, the elastic modulus of the coating has the most significant influence on the peak vibration velocity, while none of the parameters show a statistically significant effect on the peak stress. The bottom-enriched distribution of resonant aggregates does not degrade the overall vibration suppression performance; instead, a periodic arrangement exhibits superior overall performance due to the combined effects of local resonance and Bragg scattering. A four-layer resonant aggregate structure with optimized parameters achieves 93.5% attenuation rate of impact energy. This study provides theoretical references for material selection, parameter design, and process control in metaconcrete.

    Sensitivity of Absorption Behavior of Superabsorbent Polymers in Cementitious Materials
    YANG Jin, LIU Xiao, HE Xingyang, SU Ying, WANG Jinfu
    2026, 45(7):  2324-2334.  doi:10.16552/j.cnki.issn1001-1625.2026.0034
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    This study systematically compared the water absorption behavior in cementitious materials environments of two superabsorbent polymers (SAP): sodium polyacrylate superabsorbent polymer (AA-SAP) and polyacrylamide superabsorbent polymer (AM-SAP). The effects of cementitious material type, polycarboxylate ether (PCE) dosage, stirring rate, ambient temperature, and external pressure were investigated. Results show that AA-SAP, due to electrostatic repulsion from its ionic structure, absorbs water significantly faster than AM-SAP, which relies on hydrogen bonding. In pore solutions of different cementitious materials, geopolymer systems most strongly suppress SAP swelling because of their high ionic strength. The water absorption capacity of AA-SAP has an optimal response range to PCE dosage, while the water absorption capacity of AM-SAP continuously decreases with increasing PCE content. Higher stirring rates, leveraging the Bernoulli effect, promote swelling, with a more pronounced response in AA-SAP. Elevated temperature enhances the swelling of the two types of SAPs and thus improves water absorption capacity, while external pressure suppresses the network expansion of the two types of SAPs, leading to a reduction in water absorption ratio. The absorption behavior of SAP is governed by both molecular structure and external environment: AA-SAP performs better under low ionic strength, low-to-medium shear, or warmer conditions, while AM-SAP shows greater stability in high ionic strength or high-pressure settings. The findings provide both theoretical insights and practical guidance for the application of different types of SAPs in concrete.

    Solid Waste and Eco-Materials
    Effect of Circulating Fluidized Bed Slag Particle Size on Properties of Cement-Based Composite Cementitious Materials
    JING Hongyu, DUAN Siyu, YANG Songqiao, WANG Yonggang, ZHOU Dongdong, LU Guangjun, MA Zhibin
    2026, 45(7):  2335-2346.  doi:10.16552/j.cnki.issn1001-1625.2026.0038
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    To promote the resource utilization of circulating fluidized bed slag (CFBS) and reduce carbon emissions in the cement industry, this study prepared CFBS with different particle sizes through mechanical grinding and incorporated it as a supplementary cementitious material in cement blends. Firstly, the particle size distribution, specific surface area and microstructure of CFBS with different grinding time were analyzed. Then, the effect of CFBS on the workability and mechanical properties of the composite cementitious materials was investigated. The hydration characteristics of composite cementitious materials were further examined using XRD, TG-DTG, FT-IR, and SEM. The results indicate that CFBS grinding for 45 min has the best refining effect, with a median particle size D50 of 8.69 μm and a specific surface area of 870 m2/kg. Exceeding the optimal grinding time will lead to particle agglomeration and an increase in D50. The reduction of particle size can effectively stimulate the activity of CFBS, enabling the composite cementitious system to exhibit micro-expansion behavior compared to the pure cement system, and achieving better mechanical properties and the shortest setting time at the minimum D50. The reduction in CFBS particle size accelerates the hydration rate of cementitious system and promotes the formation of C-(A)-S-H gel and ettringite, resulting in a denser structure and superior mechanical properties. This study provides reference for the design and performance optimization of composite cementitious materials based on CFBS particle size regulation.

    Effect of Wet Grinding Carbonized Steel Slag on Properties and Microstructure of Beta-Hemihydrate Phosphogypsum
    JIN Zihao, ZOU Ziyong, HE Xingyang, SU Ying, CHEN Shuqin
    2026, 45(7):  2347-2356.  doi:10.16552/j.cnki.issn1001-1625.2026.0031
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    This study addressed the needs of low-carbon development in building materials and solid waste resource utilization by proposing the use of wet grinding carbonized steel slag-modified low-carbon beta-hemihydrate phosphogypsum to develop a novel high-performance low-carbon gypsum cementitious material. Results demonstrate that wet grinding carbonized steel slag significantly improves both the working properties and water resistance of beta-hemihydrate phosphogypsum, with mechanical properties degradation mitigated by extended carbonization time. The system carbonized for 60 min exhibits optimal comprehensive performance, maintaining working and mechanical properties while achieving substantial enhancement in water resistance. The formation of “dual-phase” composite structures between CaCO3 and calcium sulfate dihydrate (CaSO4·2H2O) exerts a certain negative effect on gypsum’s mechanical properties, yet effectively protects its crystal structure and enhances water resistance.

    Mechanism of Mechanical and Thermal Activation to Improve Activity of Ferronickel Slag
    LYU Peng, LU Boyong, QIAN Lun, HUANG Shenye, SONG Jiaxin, XIE Longjie, HUANG Wei
    2026, 45(7):  2357-2367.  doi:10.16552/j.cnki.issn1001-1625.2025.1179
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    To achieve efficient resource utilization of ferronickel slag, this study systematically investigated the influence of mechanical and thermal activation on its pozzolanic activity. The particle characteristics, crystal structure, mechanical properties, and electrochemical behavior of ferronickel slag under different activation conditions were comprehensively characterized by laser particle size analysis, X-ray diffraction (XRD), specific strength method, and electrochemical impedance spectroscopy characterization method. The results indicate that mechanical activation for 60 min can significantly refine the particle size and induce the lattice amorphization, so that the 28 d activity index of ferronickel slag is increased to 0.88. Thermal activation at 500 ℃ effectively destabilizes the crystalline phases and enhances the dissolution of active components, so that the 28 d activity index of ferronickel slag is 0.93. Electrochemical analysis further reveals that these optimized conditions significantly increase the charge transfer resistance of the system and encourage the development of a denser microstructure. This study clarifies the optimal pathways for enhancing the activity of ferronickel slag through mechanical and thermal activation, providing a foundation for its effective application in cementitious materials.

    Carbon Accounting Method for Cement under Different Steel Slag Treatment Methods Based on Material Genes
    DU Liwentao, REN Xuehong, ZHANG Hongtao, YE Jiayuan, ZHANG Wensheng
    2026, 45(7):  2368-2378.  doi:10.16552/j.cnki.issn1001-1625.2026.0050
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    Traditional carbon emission calculation methods typically employ industry or national average emission factors, which cannot accurately reflect the regulatory mechanism of cement’s mineral formation characteristics on carbon emissions during the reaction process. These methods focus on inventory analysis and aggregation of energy consumption and emissions in processes such as raw material grinding, clinker calcination, and cement grinding, but fail to address the fundamental issue of where energy is consumed at the molecular level. However, the final performance and environmental impact of cement are fundamentally determined by its mineral composition.

    Based on the concept of material genome, generally understood as the basic structural unit that maintains the intrinsic characteristics of materials, this paper proposed a material genome-based carbon emission accounting method utilizing the four main minerals of cement. By incorporating the regulatory mechanism of thermodynamic characteristics of materials during the reaction process on carbon emissions, a material genome-based carbon emission accounting model was constructed. This model linked microscopic mineral thermodynamic data with macroscopic industrial production parameters to reveal the impact pathways of different steel slag utilization methods in cement production on carbon emissions, and compared them with traditional calculation methods.

    The results show that carbon emission values calculated by the material genome accounting method fluctuate within 2.86% to 4.07% compared to those calculated by traditional methods, indicating close agreement. Meanwhile, compared to traditional methods, it better reflects the impact of changes in mineral composition ratios on carbon emission values and more accurately calculates carbon emissions for various types of solid waste cement. This facilitates direct accounting of product carbon emissions through terminal product composition and guides formula design. In different application cases such as using steel slag as alternative raw material for cement production, cement admixture, and carbonated cementitious material, cement prepared using carbonated steel slag powder exhibits the lowest carbon emission intensity ratio. After excluding the impact of transportation, the carbon emission intensity ratio is 16.04 kgCO2/MPa. Meanwhile, without considering variable factors such as transport distance, its overall carbon emission is also relatively the lowest, with only 726.62 kgCO2 emitted per ton of cement. For steel slag used as alternative raw material and steel slag phase-separated clinker technology, the carbon emission values of the two are similar, but the carbon emission of steel slag phase-separated clinker technology in the process and fuel stages is 3.47 kgCO2/t lower than that of steel slag as alternative raw material. Additionally, if road transportation is adopted, when the transport distance exceeds 140 km for steel slag as alternative raw material, the carbon reduction effect of steel slag approaches zero; for cement prepared with steel slag treated by high-temperature reconstruction, cement admixture, carbonated cementitious material, and phase-separated clinker technology, these distances are 233, 240, 263, and 109 km, respectively. Therefore, the transportation distance radius for steel slag utilization should not exceed 300 km. The material genome method can reflect the regulatory mechanism of thermodynamic characteristics of materials on carbon emissions during the reaction process, providing data basis for cement enterprises to screen and optimize steel slag utilization schemes.

    Rapid Assessment of Shrinkage Performance and Its Mechanism of Alkali-Activated Slag via Vacuum Dehydration
    TIAN Chenglong, TAO Yuan, LIU Leping, XIANG Jichun, CUI Xuemin, HE Yan
    2026, 45(7):  2379-2388.  doi:10.16552/j.cnki.issn1001-1625.2026.0012
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    Aiming at the problems of large shrinkage rate and long test cycle of alkali-activated slag (AAS), this study used vacuum dehydration technology to quickly evaluate its shrinkage performance, and studied the influence mechanism of vacuum dehydration temperature (40, 50, 60 ℃) on the shrinkage performance and microstructure of AAS. By monitoring the dynamic changes of AAS internal relative humidity and pore solution surface tension, combined with multi-scale microscopic analysis technology, the coupling law of temperature-moisture migration-structure evolution was revealed. The results show that vacuum dehydration significantly changes the shrinkage process of AAS. The early shrinkage of AAS is accelerated, and the total shrinkage rate at 28 d is significantly reduced. The shrinkage reduction effect after 40 ℃ treatment is the best. Moderate temperature rise ( 40 to 50 ℃) can promote the removal of free water and optimize the pore structure. The increased capillary pressure can effectively reduce the shrinkage stress in the early viscoplastic stage of AAS material through the synergistic effect of pore size optimization and creep dissipation. However, too high temperature (60 ℃) will cause the capillary pressure accumulation rate to exceed the creep dissipation capacity, causing stress-strain mismatch, which in turn induces microcracks and increases porosity.

    Effect of Natural Gypsum Content on Hydration and Performances of High-Alumina Ladle Slag Based Compound Cementitious Materials
    ZHANG Liu, GONG Ming, DING Pan, ZHOU Fei, YANG Fengyuan, LU Zhongyuan, LI Jun
    2026, 45(7):  2389-2396.  doi:10.16552/j.cnki.issn1001-1625.2025.1291
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    High-alumina ladle slag is a solid waste generated during the secondary refining process of crude steel. Its composition, structure, and properties are similar to those of aluminate cement, suggesting its potential use as a low-grade aluminate cement. In this study, a compound cementitious material was prepared using high-alumina ladle slag and natural gypsum, and the effect of natural gypsum content on its hydration and performances was investigated. The results show that the incorporation of natural gypsum reduces the water requirement for normal consistency of the compound cementitious material. Specifically, for compound cementitious material containing 40% to 60% (mass fraction, same below) natural gypsum, the water requirement for normal consistency decreases to approximately 27.6%. The setting and hardening of the compound cementitious material are accelerated compared to pure high-alumina ladle slag. For compound cementitious material with 10% to 40% natural gypsum, the initial setting time ranges from 18 min to 24 min, and the final setting time from 64 min to 71 min. Further increasing the natural gypsum content prolongs the setting time. As the natural gypsum content increases, the compressive strength of the compound cementitious material mortars increases first and then decreases. The compound cementitious material mortar containing 50% natural gypsum exhibits the highest 28 d compressive strength, reaching 29.8 MPa, although it remains lower than that of the pure high-alumina ladle slag mortar. An appropriate amount of natural gypsum mitigates the flexural strength regression observed in high-alumina ladle slag mortars. The compound cementitious material mortars with 40% and 50% natural gypsum show no flexural strength regression, achieving a 28 d flexural strength of approximately 6.0 MPa, which is higher than that of the pure high-alumina ladle slag mortar. The 28 d drying shrinkage of the compound cementitious material mortars increases first and then decreases with increasing natural gypsum content. The compound cementitious material mortar with 10% natural gypsum exhibits the highest 28 d drying shrinkage rate of 0.073 2%. In contrast, the compound cementitious material mortars with 30% to 60% natural gypsum show lower drying shrinkage than the pure high-alumina ladle slag mortar. Natural gypsum significantly influences the hydration of high-alumina ladle slag. It preferentially reacts with calcium aluminate in the high-alumina ladle slag and its hydration products to form ettringite (AFt), reducing the content of metastable hydration phases and leading to a more stable hydration structure in the compound cementitious material system.

    Mechanical Properties of Glass Powder-Modified Polypropylene Fiber-Reinforced Cementitious Composites
    WANG Fuhuan, LI Yanjie, LYU Haoping, YANG Lingqiang
    2026, 45(7):  2397-2407.  doi:10.16552/j.cnki.issn1001-1625.2025.1265
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    This study aims to systematically investigate the mechanical properties and micro-mechanisms of cementitious composites reinforced with glass powder (GP) and modified polypropylene fibers, determine the optimal mix proportion through multi-index optimization, and ultimately develop an eco-friendly high-performance fiber-reinforced cementitious composite. The experiment employed varying proportion of GP as a replacement for fly ash, along with modified polypropylene fibers of 6, 12, and 20 mm lengths in single doping or pairwise hybrid combinations. The workability and mechanical properties of the fiber-reinforced cementitious composites were systematically investigated through flowability tests, flexural tests, compressive tests, tensile tests, and four-point bending tests. SEM was utilized to explore the microstructural mechanisms by which GP and modified polypropylene fibers enhance the performance of these composites. Finally, a multi-factor grey relational decision-making model was applied to determine the optimal mix proportion. The results demonstrate that increasing the GP replacement ratio significantly improves the mechanical properties of the fiber-reinforced cementitious composites. At a 100% replacement rate of GP, the flexural strength of specimens increases by up to 79.28%, compressive strength by up to 40.72%, tensile strength by up to 80.00%, and the toughness index reaches a maximum of 30.962. SEM analysis reveals that GP particles tightly bond with hydration products and embed densely within the matrix, markedly enhancing the compactness of the cementitious composite and thereby improving its mechanical properties. Based on the grey relational decision-making model, the optimal formulation is identified as 100% GP replacement combined with 20 mm modified polypropylene fibers, which exhibits significant overall performance enhancement.

    Effects of Recycled Wind Turbine Blade Fibers and Glass Fibers on Properties of Portland Cement
    YU Zhejun, WANG Jingran, ZHANG Jinhua, HAN Bingqiang, NI Yue’e
    2026, 45(7):  2408-2418.  doi:10.16552/j.cnki.issn1001-1625.2026.0062
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    To tackle the disposal dilemma of decommissioned wind turbine blades and explore their potential for high-value utilization in construction materials, this study comparatively analyzed the effects of recycled wind turbine blade fibers (RWTBF) and glass fibers at different dosages (0.5%, 1.0%, and 1.5%, mass fraction) on the hydration process of Portland cement. The research focused on the effects of these two fiber types on the mechanical properties and microstructure of the cement matrix. The results indicate that the incorporation of both fibers prolongs the initial and final setting time of the cement, exerting a slight retarding effect on the early hydration process. Regarding mechanical performance, RWTBF demonstrates a more pronounced reinforcing effect. At 28 d, the specimens with 1.5% RWTBF achieve a peak flexural strength of 11.7 MPa, significantly outperforming the 8.8 MPa of the control group and the 9.4 MPa of the equivalent glass fiber group. Concurrently, compared to the baseline compressive strength of 68.7 MPa for the control group, the compressive strength of the 1.5% RWTBF group increases to 71.4 MPa, while that of the equivalent glass fiber group rises to 70.9 MPa. Microstructural analysis reveals that, compared to glass fibers, RWTBF constructs a more effective network structure within the cement matrix, thereby substantially enhancing the flexural strength of the paste. In conclusion, the application of RWTBF in cementitious materials not only effectively improves material performance but also provides a viable pathway for the high-value recycling of wind energy waste.

    Influence Mechanism of Silica Fume-Fly Ash Co-Doping on Strength Evolution and Impermeability of Concrete
    XIAO Wei, LI Yihang, WANG Dongqi, ZHONG Zuliang, ZHOU Ren, ZHU Kaixin
    2026, 45(7):  2419-2427.  doi:10.16552/j.cnki.issn1001-1625.2026.0110
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    In order to promote the efficient utilization of industrial solid waste such as silica fume and fly ash in the field of building materials and promote the green and low-carbon development of concrete materials, this paper used slump, slump flow, uniaxial compressive strength, impermeability test and SEM-EDS microscopic analysis method. Four groups of concrete with different admixture systems were systematically studied, including the reference group JZ (C30 concrete), the single-doping silica fume group D1 (8% (mass fraction) silica fume) and the composite group D2 (8% silica fume+10% (mass fraction) fly ash) and D3 (8% silica fume+20% fly ash). The results show that the D1 group exhibits the highest uniaxial compressive strength at both 1 and 3 d. In particular, its 3 d uniaxial compressive strength reaches 17.9 MPa, representing an increase of approximately 15% compared with 15.6 MPa for JZ group. The D2 group achieves the highest 28 d uniaxial compressive strength, at 38.6 MPa, and also has the lowest water penetration height, indicating the best overall performance. Although the D3 group workability is superior to the D2 group, its uniaxial compressive strength and impermeability are both inferior to those of the D2 group. The co-doping of silica fume and fly ash promotes the secondary hydration reaction, which is conducive to the further formation of hydration products and the densification of matrix. In general, silica fume dominates the early structural densification and uniaxial compressive strength formation, while fly ash improves the durability of concrete mainly through the reconstruction of pore structure and the blocking of infiltration channel in the later stage. The synergistic improvement of mechanical properties and impermeability can be achieved by the combination of silica fume and fly ash.

    Effects of Calcium Sulfate Whiskers on Hydration and Microstructure of Fly Ash-Cement Composites
    ZHANG Wencong, BAO Qinfan, WANG Yuqiu, MAN Baoliang, HUANG Guo, GUO Rongxin
    2026, 45(7):  2428-2437.  doi:10.16552/j.cnki.issn1001-1625.2026.0080
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    The high-value co-utilization of solid waste has become an important way to promote the green and low-carbon development of cement-based materials. This paper investigated the effects of 1%, 3%, and 5% (mass fraction) calcium sulfate whiskers on the microstructure, hydration reaction, and mechanical properties of fly ash-cement composites. Experimental results show that the addition of 1% calcium sulfate whiskers promote the hydration reaction of aluminate phases and the formation of ettringite, thereby optimizing the microstructure density and mechanical properties of fly ash-cement composite materials. However, when the calcium sulfate whisker content over 1%, with the increase of calcium sulfate whisker content, the excessive sulfate ions lead to the formation of a large amount of expansive ettringite in the later stage, causing cracks in the microstructure and thus reducing the strength of fly ash-cement composite materials. Comprehensive analysis shows that calcium sulfate whiskers exhibit optimal performance at 1% content in the fly ash-cement composite material system. This study provides a theoretical basis for the design of calcium sulfate whiskers in fly ash-cement composite materials.

    Mechanical Properties and Reaction Characteristics of Fly Ash-Calcium Carbide Residue-Desulfurization Gypsum Cementitious Materials
    WANG Yue, CONG Peiliang
    2026, 45(7):  2438-2447.  doi:10.16552/j.cnki.issn1001-1625.2026.0104
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    To achieve the efficient co-utilization of industrial solid wastes including fly ash (FA), calcium carbide residue (CCR), and desulfurization gypsum (DG), 21 different mix proportion was designed to prepare ternary cementitious system. The primary objective is to elucidate the influence of material composition on workability, mechanical performance, and microstructural evolution. Furthermore, quantitative relationships between key molar ratios and strength development are established. Thermodynamic modeling is also employed to predict long-term phase stability, providing insights into the durability of the material. A total of 21 mix proportion were designed with varying mass ratios of FA, DG, and CCR at a fixed water-to-binder ratio of 0.3. The fluidity, setting time, and compressive strengths at 7 and 28 d were systematically evaluated. The phase composition and microstructure of the hydration products were characterized by X-ray diffraction (XRD), thermogravimetric-differential thermogravimetric analysis (TG-DTG), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). Thermodynamic simulations were performed using GEM-Selektor software with the CEMDATA 18 database to predict equilibrium phase assemblages. The results show that paste fluidity generally decreases with increasing CCR content due to the porous structure and water absorption capacity of CCR, while the setting time shortens with higher DG content, attributing to the rapid hydration of hemihydrate. Spearman correlation analysis of the key parameters sulfur-to-aluminum molar ratio (S/Al) and calcium-to-silicon molar ratio (Ca/Si) reveals that the 7 d compressive strength exhibits a strong positive correlation with S/Al, indicating that early strength is primarily governed by the formation of gypsum and ettringite networks. In contrast, the 28 d compressive strength shows a strong positive correlation with the Ca/Si, indicating that long-term performance is primarily dependent on Ca/Si. When the mass ratio of FA, DG, and CCR is 70∶5∶25, the 28 d compressive strength reaches the maximum value of 15.04 MPa. Its microstructure exhibits an interwoven network of calcium aluminosilicate hydrate (C-(A)-S-H) gel and ettringite, contributing to a dense matrix. XRD and FTIR analyses confirm that the main reaction products include gypsum, ettringite, and C-(A)-S-H gel. TG-DTG results further reveal that, for three representative mixes with different CCR content, the weight loss associated with ettringite decomposition is consistent with their corresponding strength trends. Thermodynamic simulations were conducted with a fixed FA content of 70% by mass, varying the relative proportions of DG and CCR. Additional simulations were also performed with fixed FA content of 75% and 80%. The simulations predict that under long-term equilibrium, systems with high DG content tend to form more gypsum, and ettringite may disappear when DG exceeds a critical threshold. In contrast, systems with higher CCR content favor the formation of C-(A)-S-H gels. The simulations also identify the potential formation of stratlingite and gibbsite as stable phases under long-term equilibrium. These phases are not observed in the actual specimens at 28 d, likely due to their slow formation kinetics, which are limited by the relatively short curing age. These findings provide a reference for evaluating the long-term durability and phase stability of the material.

    Optimization of Mix Proportion and Micro-Mechanism Study of Multi-Source Solid Waste-Based Cementitious Backfill
    WANG Yanheng, ZHANG Jiawei, REN Kai, YAN Guochao, KONG Shaoqi, LI Gang, LI Boyu, WU Kuangkuang
    2026, 45(7):  2448-2465.  doi:10.16552/j.cnki.issn1001-1625.2026.0067
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    Addressing the existing research gap in understanding the synergistic effects and optimal mix design of multi-source solid waste-based cementitious backfill(MSSWCB), as well as the unclear hydration mechanisms, strength development, and microstructural evolution of individual components within complex systems, this study utilized coal gangue as aggregate, fly ash and steel slag as primary cementitious components, carbide residue and desulfurization gypsum as composite activators, supplemented with a small amount of cement (adding an amount equal to the mass of coal gangue), to prepare a MSSWCB for mine backfilling. Through orthogonal experiments and microscopic testing methods, the mechanical properties and bonding mechanism of this material were investigated. Results indicate that the compressive strength of MSSWCB increases significantly with curing age, with average compressive strength at 3, 7, and 28 d being 2.058, 3.604, and 7.211 MPa, respectively. The optimal mix ratio (the mass ratio of coal gangue aggregate, cement, fly ash, steel slag, calcium carbide slag, desulfurization gypsum, water is 1∶1∶1.9∶0.9∶0.3∶0.15∶1.615) achieves a 28 d compressive strength of 12.96 MPa. Analysis of influencing factors indicates that early strength is primarily controlled by the water-binder ratio, while mid-term strength is jointly affected by both the water-binder ratio and the amount of calcium carbide slag added. The key factor affecting later-stage strength is the fly ash content. Through microscopic analysis, the hydration products of MSSWCB at different curing stages are revealed: early-stage products are dominated by ettringite (AFt), mid-stage saw significant generates calcium silicate hydrate (C-S-H) and calcium aluminum silicate hydrate (C-A-S-H) gels, and late-stage C-(A)-S-H gel becomes the primary cementing phase. Structural densification forms the microscopic basis for strength development. This study provides experiment support and technical guidance for the resource utilization of multi-source solid waste and the development of green mine backfill cementitious materials.

    Preparation and Properties of Solid Waste-Based Ecological Mine Backfill Materials under Multi-Factor Interactions
    HAO Yunhong, TONG Haiyan, WANG Dongmin, SUN Hao, DU Genjie
    2026, 45(7):  2466-2477.  doi:10.16552/j.cnki.issn1001-1625.2025.1229
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    Using fly ash and desulfurization gypsum as the main raw materials, a multi-solid waste, high foaming, high rheological, medium-strength solid waste-based ecological mine filling material was prepared in this paper. The influences of water-binder ratio, fly ash content, foaming ratio and other factor on the slump flow and 28 d compressive strength of backfill material were analyzed. The properties of solid waste-based ecological mine backfill material were studied through fluidity tests, strength tests, and microstructure tests. The results indicate that the basic mix proportion of material is as follows: water-binder ratio of 0.51 to 0.55, fly ash content of 55% to 60% (mass fraction), desulfurization gypsum content of 15% to 20% (mass fraction), foaming ratio of 2.0 times to 3.0 times, and water reducer content of 0.6% to 0.8% (mass fraction). At this mix proportion, the slump flow of the material is 226 mm to 273 mm and the 28 d compressive strength is 2.11 MPa to 5.93 MPa. When the solid waste content is 60% to 70%, desulfurization gypsum and fly ash form a synergistic system with a mass ratio of approximately 1∶4, generating an interlocking structure of calcium silicate hydrate gel and ettringite. The microstructure confirms that the macroscopic mechanical properties of material have been improved. The hydration products can effectively immobilize heavy metals, with low ecological risk, meeting the environmental safety requirements for mine backfill.

    Durability and Microstructure of Phosphogypsum-Slag-Based All-Solid-Waste Cementitious Material Regulated by Red Mud and Recycled Cement Powder
    LIU Xin, LI Mingyang, ZHANG Xihe, LAN Shaoding, GAO Xu
    2026, 45(7):  2478-2490.  doi:10.16552/j.cnki.issn1001-1625.2025.1258
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    In this paper, phosphogypsum-slag-based all-solid-waste cementitious material was developed using phosphogypsum (PG), slag, recycled cement powder (RCP), red mud (RM), and quicklime. The individual and synergistic effects of RCP and RM on mechanical properties, durability, and microstructure were characterized. The results indicate that the incorporation of RCP and RM significantly enhances the mechanical properties and durability of the cementitious material. The specimen with 10% (mass fraction) RCP and 10% (mass fraction) RM exhibits relatively superior performance. In comparison to the PG-slag-based system, the 28 d compressive strength and flexural strength increase by 57.1% and 57.4%, reaching 43.2 and 7.4 MPa, respectively. Simultaneously, the non-steady-state chloride migration coefficient and drying shrinkage decrease by 42.5% and 43.6%, while the sulfate corrosion resistance coefficient is elevated from 73.6% to 85.6%. RCP serves as a physical filler and provides chemical activity, offering nucleation site and active component for the hydration reaction. Additionally, RM raises the alkalinity of the system and introduces extra aluminosilicate minerals, which accelerates the dissolution and polymerization of precursors, and stimulates the potential pozzolanic activity of RCP. RCP and RM synergistically promote the formation of calcium aluminosilicate hydrate gel and maintain a considerable amount of ettringite, consequently optimizing the composition of hydration products, ultimately achieving a comprehensive improvement in pore structure densification and macroscopic performance. This study is expected to provide a technical reference for the development of green cementitious materials and the resource utilization of solid waste.

    Ceramics ang Glass
    Effect of Y2O3 Additive on Properties of Molten Salt-Assisted Synthesis of Al2O3-SiC Composite Powders and Resulting Ceramic Materials
    SUN Yijing, ZHENG Lijun, LUO Xudong, GAO Yimeng, QU Jiayin
    2026, 45(7):  2491-2498.  doi:10.16552/j.cnki.issn1001-1625.2026.0068
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    To further investigate the preparation process of Al2O3-SiC composite ceramics, Al2O3-SiC composite powder was successfully synthesized via a molten-salt-assisted method using silica fume, aluminum powder, and carbon black as raw materials, Y2O3 as the additive, and NaCl and KCl as the molten salt medium. The effects of synthesis temperature and Y2O3 content on the phase composition and microstructure were investigated. The results show that the principal crystalline phases are α-Al2O3 and β-SiC. With Y2O3 content increasing from 0% to 3%(mass fraction), SiC whiskers are formed with lengths of 0.5 μm to 3.0 μm and diameters ranging from 20 nm to 70 nm. The growth mechanism study reveals that Y2O3 plays an important role in the formation of SiC whiskers, following a vapor-solid (V-S) growth mechanism. For the sample with 3%Y2O3 sintered at 1 500 ℃ for 4 h via pressureless sintering, the obtained Al2O3-SiC composite ceramic material exhibits a apparent porosity of 25.3%, a bulk density of 1.98 g·cm-3, and a compressive strength of 16.4 MPa.

    Investigation of Crystallization Behavior and Properties of Transparent Na2O-ZnO-MgO-Al2O3-SiO2 Glass-Ceramics
    CAO Cheng, LI Xuerong, HE Siyi, GENG Chao, SUN Wenhao, XU Wenpeng, JIANG Demei, WANG Haifeng
    2026, 45(7):  2499-2509.  doi:10.16552/j.cnki.issn1001-1625.2025.1316
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    Transparent Na2O-ZnO-MgO-Al2O3-SiO2 (NZMAS) glass-ceramics were prepared by a melting and heat treatment method. This study systematically investigated the effect of Na2O content ranging from 0% to 10% (mole fraction) on the glass structure, crystallization behavior, and resultant properties. The results indicate that with increasing Na2O content, both the glass transition temperature and crystallization temperature exhibit a decreasing trend. In samples with 0% and 2% Na2O, the primary crystalline phases are MgAl2Si3O10 and cordierite. When the Na2O content reaches 4%, the MgAl2Si3O10 phase disappears, and cordierite becomes the dominant phase. Further increasing the Na2O content to 10% leads to the precipitation of the nepheline phase. For the base glass containing 8% Na2O, heat-treated at 820 ℃ for 5 h (nucleation) followed by 970 ℃ for 1 h (crystallization), the resulting glass-ceramics exhibit uniformly distributed fine crystals with an average grain size of approximately 105.9 nm and a visible light transmittance of up to ~80%. It exhibits high Vickers hardness and flexural strength, measuring 7.31 GPa and 134 MPa, respectively. After undergoing ion exchange in a pure KNO3 salt bath at 460 ℃ for 4 h, this sample achieves a Vickers hardness of 7.81 GPa and a flexural strength of 375 MPa.This research demonstrates that the developed glass-ceramics possess a combination of excellent optical and mechanical properties, showing promising application potential in fields such as mobile terminal cover glass.

    Functional Materials
    Preparation and Performance of Solid Oxide Fuel Cells Using Low-Concentration Methane as Fuel
    ZHU Lihua, TIAN Qianwen, CHENG Siyi, XU Feng, LI Jiazhe, CHEN Xiye
    2026, 45(7):  2510-2519.  doi:10.16552/j.cnki.issn1001-1625.2026.0079
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    Solid oxide fuel cells can achieve clean and efficient conversion of low-concentration methane, and they also possess multiple values such as safety, resource utilization, and environmental protection. Based on the synthesis of anode material La0.3Sr0.7Fe0.7Ti0.3O3 (LSFT) by sol-gel method, electrolyte material Sm0.2Ce0.8O1.9 (SDC) and cathode material La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) by the combined calcium disodium edetate (EDTA-CA) complexation method, an electrolyte supported solid oxide fuel cell LSFT/SDC/LSCF was prepared. The electrochemical performance of the cell was tested using low-concentration methane as the fuel within the temperature range of 650 ℃ to 800 ℃. The results show that the synthesized LSFT and LSCF have a relatively pure cubic perovskite structure with developed pores, while SDC has a dense cubic fluorite structure. The prepared cell LSFT/SDC/LSCF can achieve the integration of electricity and hydrogen production. The higher the concentration of methane in the fuel gas is, the better the electrochemical performance of the cell is. Moreover, the performance of the cell is significantly affected by temperature. When using a low-concentration methane (with a volume concentration of 30%) as the fuel gas, the polarization impedance of the cell at 800 ℃ is 0.15 Ω·cm2, the methane conversion is 30.4%, and the hydrogen selectivity is 45.8%. The research results can provide a reference for in-depth studies on low-concentration methane, especially the utilization of low-concentration coal mine gas based on solid oxide fuel cells.

    Dual Lithium Salt Regulation and Battery Performance of F127/Cellulose Composite Solid Electrolyte
    YOU Xiang, TANG Junyan, WU Yang, WANG Wei, WANG Xinxin, YI Xiao, YANG Changchang, KONG Linghui, ZHANG Tao, ZHANG Gang
    2026, 45(7):  2520-2530.  doi:10.16552/j.cnki.issn1001-1625.2025.1208
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    To address the poor interfacial stability between polyether-based solid electrolytes and lithium metal anodes, this study adopted a dual-salt strategy to design and prepare an F127/cellulose composite solid electrolyte. A homogeneous polymer slurry was fabricated by blending a LiTFSI and LiDFOB dual-salt system with F127 using a hot-melting method, which was then infiltrated into a porous cellulose membrane to obtain a structurally dense composite electrolyte. The results indicate that the introduction of LiDFOB significantly improves the electrolyte/lithium metal interface performance and promotes the formation of a stable solid electrolyte interphase (SEI) layer. Electrochemical tests reveal that the dual-salt electrolyte achieves an ionic conductivity of 2.0×10-4 S·cm-1 at 60 ℃ and an enhanced lithium-ion transference number of 0.31. Li/Li symmetric cells assembled with this electrolyte exhibit an increased limiting current density of 0.5 mA·cm-2 and maintain stable cycling for over 2 000 h under the conditions of 0.1 mA·cm-2 and 0.1 mAh·cm-2. LFP/Li full cells deliver a discharge capacity of 111.11 mAh·g-1 at a 2.0 C rate, with a capacity retention of 66.38% after 800 cycles at 0.5 C. This work provides a simple and feasible dual-salt strategy that synergistically enhances ionic conductivity and interfacial stability of the electrolyte, offering new insights for the design of electrolytes for high-energy-density solid-state lithium metal batteries.

    Synergistic Modification of Boron Nitride with Silver Loading and Hydroxylation for Enhanced Photocatalysis
    SHENG Hailong, GENG Yongjuan, ZHOU Anjie, LI Shaochun
    2026, 45(7):  2531-2539.  doi:10.16552/j.cnki.issn1001-1625.2026.0017
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    To enhance the visible-light photocatalytic activity of hexagonal boron nitride (h-BN), a synergistic modification strategy combining edge hydroxylation and silver nanoparticle loading was proposed and implemented. The Ag/h-BN-OH composite was successfully synthesized via a hydrothermal process to introduce B—OH groups at the h-BN edges, followed by a self-assembly and hydrothermal reduction step to anchor silver nanoparticles. The material’s structure and composition were characterized by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. Its optoelectrochemical properties were systematically investigated using ultraviolet-visible diffuse reflectance spectroscopy, electrochemical impedance spectroscopy, transient photocurrent response, and electron paramagnetic resonance spectroscopy. The results indicate that edge hydroxylation significantly increases the loading amount of silver nanoparticles (up to 5.3%). The surface plasmon resonance effect of the silver nanoparticles effectively extends the light absorption edge to 500 nm and reduces the apparent band gap to 2.09 eV, thereby broadening the visible-light response. The composite demonstrates superior charge separation efficiency and enhanced generation capability of hydroxyl radicals. Under visible-light irradiation, it achieves a high degradation rate of 91% for Rhodamine B within 60 min. This study confirms that constructing a synergistic system comprising edge hydroxyl active sites and plasmonic metals can effectively address the core limitations of wide-bandgap h-BN, namely rapid recombination of photogenerated carriers and low visible-light utilization efficiency, offering a new pathway for designing efficient boron nitride-based photocatalytic materials.

    Influencing Factors of Dispersion Stability and Photocatalytic Performance of Nano-TiO2 in Water
    LI Yuxiang, ZHAO Rong, LU Bo, YAN Wenli, MA Yibo, FAN Haihong, CHENG Feng
    2026, 45(7):  2540-2548.  doi:10.16552/j.cnki.issn1001-1625.2025.1251
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    The dispersion stability of nano-TiO2 greatly affects tis application performance. In this paper, nano-TiO2 with different particle sizes were prepared by the sol-gel method and dispersed in water. The dispersion stability of nano-TiO2 under different conditions was characterized and analyzed, and its photocatalytic performance in degrading Rhodamine B was investigated. The results show that the sedimentation rate of nano-TiO2 in water decreases with the decrease of particle size of nano-TiO2. The dispersion stability of the nano-TiO2 suspension is the best when pH 2. At pH 4, the sedimentation rate is high because this pH value is close to the isoelectric point. The absolute value of Zeta potential in an alkaline environment is lower than that in an acidic environment, resulting in poor stability of the nano-TiO2 suspension. Sodium hexametaphosphate exhibits the best dispersion performance on nano-TiO2. When the dosage of sodium hexametaphosphate is 30% (mass fraction), the nano-TiO2 suspension still maintains excellent stability after 10 d. Higher dispersion stability of nano-TiO2 corresponds to higher photocatalytic degradation efficiency. With nano-TiO2 of 31.0 nm, sodium hexametaphosphate as the dispersant, and pH value of the nano-TiO2 suspension adjusted to 2, the degradation rate of Rhodamine B solution reaches 90.1% at 30 min and 99.2% at 60 min, indicating that improving the dispersion of nano-TiO2 in water significantly enhances its photocatalytic efficiency.

    Repassivation of Prestressed Corroded Steel Strand in Sodium Molybdate Composite Solution
    SHAN Zhilong, ZHANG Yunsheng, ZHANG Shouqi, ZHANG Yu, LIU Qingyang, WANG Youping
    2026, 45(7):  2549-2560.  doi:10.16552/j.cnki.issn1001-1625.2026.0019
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    To extend the service life of prestressed reinforced concrete structures, this study developed a composite sodium molybdate solution for repassivation treatment of corroded steel strands. Electrochemical measurements, mechanical tests, and microstructural characterization were conducted to compare uncorroded, corroded, and repassivated steel strands. Results indicate that repassivation significantly enhances the corrosion resistance of steel strands: the potential shifts toward a more positive value, corrosion current density decreases, and the Nyquist arc widens. After repassivation, the yield strength and tensile strength of steel strands remain largely unchanged. While corrosion reduces ductility by 15%, repassivation restores 10% of the lost ductility. Bond strength between repassivated strands and concrete improves compared to uncorroded strands. Microstructural analysis reveals that the performance enhancement of the repassivated steel strands stems from the formation of a dense, needle-like film composed of molybdate and phosphate phases. These findings confirm that repassivation technology effectively restores the properties of corroded steel strands without compromising tensile performance, offering a highly promising repair solution for prestressed concrete infrastructure.

    Road Materials
    Mechanical Properties Analysis and Optimal Mix Proportion Prediction of Cement-Stabilized Crushed Stone with Recycled Aggregate
    SHEN Yanli, WEI Guanchao, WANG Peng, WANG Jiawei, XU Lei, WANG Hui, WANG Zhiling, WEI Aikui
    2026, 45(7):  2561-2572.  doi:10.16552/j.cnki.issn1001-1625.2025.1285
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    To achieve the resource recycling of waste road concrete recycled aggregate in road base courses, this study combined experimental analysis and artificial intelligence methods were employed to investigate the effects of different cement content (3.50%, 4.50%, 5.50%, mass fraction) and recycled aggregate incorporation rates (4.15%, 56.20%, 78.10%, 100.00%, mass fraction) on the maximum dry density, optimum moisture content, unconfined compressive strength, compressive resilient modulus, and splitting strength of cement-stabilized crushed stone containing recycled aggregates from waste road concrete. Based on machine learning and the genetic algorithm (GA), prediction models for the 7 and 90 d unconfined compressive strength and a gradation optimization model for recycled aggregate cement-stabilized crushed stone were established. The results indicate that higher cement content improves the mechanical properties of recycled aggregate cement-stabilized crushed stone. Increasing the recycled aggregate content reduces the maximum dry density and raises the optimum moisture content. An appropriate amount of recycled aggregate can enhance the 7 and 90 d unconfined compressive strength as well as the 90 d splitting strength, whereas the compressive resilient modulus gradually decreases with increasing recycled aggregate content. When the recycled aggregate content is 78.10% and the cement content is 5.50%, the representative values of 7 and 90 d unconfined compressive strength are 4.24 and 7.07 MPa, respectively, and the average values of 90 d splitting strength and compressive resilient modulus are 0.64 and 1 925 MPa, all of which meet the relevant specification requirements. Based on the analysis of the mechanical properties of recycled aggregate cement-stabilized crushed stone, a random forest model combined with the genetic algorithm (GA) is selected for gradation optimization, yielding a predicted 7 d unconfined compressive strength of 5.82 MPa for the optimal mixture proportion.

    Mixture Design of Siliceous Sandstone Used as Asphalt-Treated Base Based on Balanced Mix Design
    ZOU Deqiang, WAN Bing, YANG Bo, TANG Jiale, REN Jianghan
    2026, 45(7):  2573-2582.  doi:10.16552/j.cnki.issn1001-1625.2025.1294
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    To diversify aggregate sources and maximize resource utilization in highway construction, siliceous sandstone from Southwest China was evaluated as an aggregate for high-grade asphalt pavement base layers. The mechanical properties of the aggregate and the performance of the resulting mixture were investigated. To determine the optimum asphalt-aggregate ratio, two design approaches were compared: the Marshall mix design and a balanced mix design approach, aiming to balance high-temperature deformation resistance with low-temperature cracking resistance. Results indicate that the siliceous sandstone aggregate meets all standard specification requirements, exhibiting a uniaxial compressive strength exceeding 80 MPa in the natural state and 42 MPa in the water-saturated state. The Marshall mix design and the balanced mix design yield optimum asphalt content of 4.1% and 3.8%, respectively. While both designs satisfied low-temperature performance requirements, the mixture designed via balanced mix design demonstrates a dynamic stability 44.2% higher than the mixture via Marshall mix design, indicating superior suitability for high-temperature regions. Replacing mineral filler with 1.4% to 2.0% 42.5-grade ordinary Portland cement (by mass) effectively addresses the insufficient water stability revealed by the initial immersion residual stability and freeze-thaw splitting tests. Consequently, the immersion residual stability and freeze-thaw splitting strength ratios are improved by 34.2% and 36.7%, respectively, meeting specification requirements. Finally, a dynamic modulus master curve was constructed using the Sigmoidal function based on the time-temperature superposition principle. At 20 ℃ and 5 Hz, the dynamic modulus is recorded at 5 614 MPa, indicating good bearing capacity. Its use as a base layer for high-grade asphalt pavement is reasonable and feasible.