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硅酸盐通报 ›› 2026, Vol. 45 ›› Issue (7): 2438-2447.DOI: 10.16552/j.cnki.issn1001-1625.2026.0104

• 资源综合利用 • 上一篇    下一篇

粉煤灰-电石渣-脱硫石膏胶凝材料力学性能与反应特性

王月(), 丛培良()   

  1. 长安大学材料科学与工程学院,西安 710064
  • 收稿日期:2026-01-29 修订日期:2026-03-01 出版日期:2026-07-15 发布日期:2026-08-13
  • 通信作者: 丛培良,博士,教授。E-mail:congpl@chd.edu.cn
  • 作者简介:王 月(2002—),女,硕士研究生。主要从事胶凝材料的研究。E-mail:2025131066@chd.edu.cn
  • 基金资助:
    中央高校基本科研业务费专项资金资助(300102313206)

Mechanical Properties and Reaction Characteristics of Fly Ash-Calcium Carbide Residue-Desulfurization Gypsum Cementitious Materials

WANG Yue(), CONG Peiliang()   

  1. School of Materials Science and Engineering,Chang’an University,Xi’an 710064,China
  • Received:2026-01-29 Revised:2026-03-01 Published:2026-07-15 Online:2026-08-13

摘要:

为实现粉煤灰(FA)、电石渣(CCR)与脱硫石膏(DG)等工业固废的高效协同利用,本研究设计21组不同配比,制备了FA-CCR-DG三元复合胶凝材料,系统测定了浆体的工作性、7与28 d抗压强度,并利用X射线衍射(XRD)、热重-微分热重(TG-DTG)、傅里叶变换红外光谱(FTIR)及扫描电子显微镜(SEM)分析了产物的物相组成与微观结构,同时借助GEM-Selektor软件进行了热力学模拟以预测长期相演变。结果表明,浆体流动度随电石渣含量增加呈降低趋势,凝结时间随脱硫石膏含量增加而缩短。7 d抗压强度与硫铝摩尔比(S/Al)呈强正相关,而28 d抗压强度则与钙硅摩尔比(Ca/Si)呈强正相关。当粉煤灰、脱硫石膏、电石渣的质量比为70∶5∶25时,28 d抗压强度最高,达到15.04 MPa。在该配比下,试样生成了更多的C-(A)-S-H凝胶和钙矾石,产物相互穿插,结构更为密实。热力学模拟预测,长期平衡下高脱硫石膏含量体系趋向于生成更多的二水石膏相,而高电石渣含量体系趋向于生成较多的凝胶相,这为评估材料的长期耐久性提供了参考。

关键词: 胶凝材料, 工业固废, 协同激发, 力学性能, 微观结构, 热力学模拟

Abstract:

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.

Key words: cementitious material, industrial solid waste, synergistic stimulation, mechanical property, microstructure, thermodynamic simulation

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