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硅酸盐通报 ›› 2026, Vol. 45 ›› Issue (9): 3163-3173.DOI: 10.16552/j.cnki.issn1001-1625.2026.0190

• 资源综合利用 • 上一篇    下一篇

水玻璃参数对碱激发地聚物工作与力学性能的影响

周辉勇1(), 王艳朝1, 高华1, 郭威2, 凡涛涛2(), 司春棣2, 马喜报2   

  1. 1.河北石太高速公路开发有限公司,石家庄 050299
    2.石家庄铁道大学交通运输学院,石家庄 050043
  • 收稿日期:2026-03-02 修订日期:2026-04-07 出版日期:2026-09-15 发布日期:2026-10-09
  • 通信作者: 凡涛涛,博士,讲师。E-mail:fantaotao@stdu.edu.cn
  • 作者简介:周辉勇(1979—),男,高级工程师。主要从事公路工程方面的研究。E-mail:506194879@qq.com
  • 基金资助:
    河北省高等学校科学技术研究项目(QN2023178);国家自然科学基金项目(52378455);河北省交通运输厅科技计划项目(ST-202414)

Influences of Water Glass Parameters on Working Performance and Mechanical Properties of Alkali-Excited Geopolymers

ZHOU Huiyong1(), WANG Yanchao1, GAO Hua1, GUO Wei2, FAN Taotao2(), SI Chundi2, MA Xibao2   

  1. 1.Hebei Shi -Tai Expressway Development Co. ,Ltd. ,Shijiazhuang 050299,China
    2.School of Traffic and Transportation,Shijiazhuang Tiedao University,Shijiazhuang 050043,China
  • Received:2026-03-02 Revised:2026-04-07 Published:2026-09-15 Online:2026-10-09

摘要:

为探究碱激发剂参数对地聚物工作性能和力学性能的影响,以铁尾矿砂、煤矸石粉和高炉矿渣为原材料,采用固体水玻璃和液体水玻璃两种碱激发剂制备地聚物,分析水玻璃类型、模数和Na2O掺量对地聚物凝结时间、流动度、抗压强度和抗折强度的影响规律,结合SEM和XRD揭示水玻璃激发地聚物强度形成机制。结果表明,随着水玻璃模数的增加,两种碱激发地聚物的凝结时间均增大,且液体水玻璃激发地聚物的流动度、抗压强度与抗折强度呈先上升后降低趋势,最佳模数为1.6,而固体水玻璃激发地聚物的流动度呈下降趋势,抗压强度与抗折强度呈先降低后上升趋势,最佳模数为0.6。随Na2O掺量的增加,地聚物的凝结时间与流动度降低,抗压强度和抗折强度均升高,掺6%(质量分数)Na2O的地聚物综合性能最佳。液体水玻璃激发地聚物的工作性能和力学性能优于固体水玻璃激发地聚物。两种水玻璃均通过影响地聚物水化反应进程调控地聚物强度形成,其中固体水玻璃因自身溶解速率受限,使水化凝胶产物分布不均,影响了地聚物强度发展。

关键词: 碱激发地聚物, 水玻璃参数, 凝结时间, 流动度, 力学性能, 作用机理

Abstract:

To investigate the influences of alkali activator parameters on the working performance and mechanical properties of geopolymers, the geopolymers were prepared using iron tailings sand, coal gangue powder, and blast furnace slag as raw materials, employing both solid water glass and liquid water glass as alkali activators. The effects of water glass types, modulus and Na2O dosage on geopolymers setting time, flowability, compressive strength and flexural strength were analyzed. Additionally, SEM and XRD were conducted to reveal the strength development mechanism of water glass-excited geopolymers. The results indicate that as modulus of water glass increases, the setting time of both alkali-excited geopolymers extends. Liquid water glass-excited geopolymers exhibit a trend of initially increasing then decreasing flowability, compressive strength and flexural strength, with an optimum modulus of 1.6. Solid water glass-excited geopolymers show a decreasing trend in flowability, while compressive strength and flexural strength initially decreases then increases, with an optimum modulus of 0.6. As the Na2O dosage increases, the setting time and flowability of the geopolymers decrease while both compressive and flexural strength increase. The geopolymers exhibits optimal performance when the Na2O content is 6% (mass fraction). Liquid water glass-excited geopolymers exhibit superior working performance and mechanical properties compared to solid water glass-excited geopolymers. Both solid and liquid water glass are employed to modulate geopolymer strength development by influencing the geopolymerization reaction kinetics. Notably, solid water glass exhibits a relatively low dissolution rate in the alkaline activation medium, resulting in heterogeneous distribution of reaction products and consequently impeding uniform strength gain.

Key words: alkali-excited geopolymer, water glass parameter, setting time, flowability, mechanical property, reaction mechanism

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