欢迎访问《硅酸盐通报》官方网站,今天是
分享到:

硅酸盐通报 ›› 2025, Vol. 44 ›› Issue (1): 297-304.DOI: 10.16552/j.cnki.issn1001-1625.2024.0797

• 资源综合利用 • 上一篇    下一篇

钙硅比对硅酸钙矿相烧结行为和固碳能力的影响

陈平1,2, 李芳彬3,4, 向玮衡1,2, 胡成2,3, 刘俊1,3, 王启杰2,3   

  1. 1.桂林理工大学,广西绿色建材与建筑工业化重点实验室,桂林 541004;
    2.桂林理工大学,广西工业废渣建材资源利用工程技术研究中心,桂林 541004;
    3.桂林理工大学,土木工程学院,桂林 541004;
    4.桂林理工大学,有色金属矿产勘查与资源高效利用省部共建协同创新中心,桂林 541004
  • 收稿日期:2024-07-11 修订日期:2024-10-12 出版日期:2025-01-15 发布日期:2025-01-23
  • 通信作者: 向玮衡,博士,副研究员。E-mail:XWH891116@163.com
  • 作者简介:陈 平(1964—),男,博士,教授。主要从事固废资源化利用与绿色低碳胶凝材料等方面的研究。E-mail:m19978306769@163.com
  • 基金资助:
    广西青年人才专项(桂科AD22035126);广西自然科学基金(2023GXNSFBA026130);国家自然科学基金(52368029,52062009);广西绿色建材与建筑工业化重点实验室开发基金(桂科能22-J-21-19)

Effect of Calcium Silicon Ratio on Sintering Behavior and Carbon Sequestration Capacity of Calcium Silicate Mineral Phase

CHEN Ping1,2, LI Fangbin3,4, XIANG Weiheng1,2, HU Cheng2,3, LIU Jun1,3, WANG Qijie2,3   

  1. 1. Guangxi Key Laboratory of Green Building Materials and Construction Industrialization, Guilin University of Technology, Guilin 541004, China;
    2. Guangxi Engineering and Technology Center for Utilization of Industrial Waste Residue in Building Materials, Guilin University of Technology, Guilin 541004, China;
    3. College of Civil Engineering, Guilin University of Technology, Guilin 541004, China;
    4. Collaborative Innovation Center for Exploration of Nonferrous Metal Deposits and Efficient Utilization of Resources, Guilin University of Technology, Guilin 541004, China
  • Received:2024-07-11 Revised:2024-10-12 Published:2025-01-15 Online:2025-01-23

摘要: 硅酸钙固碳胶凝材料是实现建材行业绿色可持续发展的重要方向,为探明钙硅比(n(CaO)∶n(SiO2),摩尔比)对硅酸钙矿相组成和固碳能力的影响,本文通过调控钙硅比(n(CaO)∶n(SiO2)=1.8~2.2)制备了硅酸钙固碳胶凝材料,采用t-pH、XRD、TGA、SEM等技术研究了硅酸钙固碳胶凝材料的相组成、碳化硬化过程、CO2吸收率和碳化产物的演化规律。研究结果表明:γ型硅酸二钙(Ca2SiO4,γ-C2S)生成量随钙硅比的增大先增加后减少;当钙硅比不高于2.0时,硅钙石(Ca3Si2O7,C3S2)生成量随钙硅比的减小而增多,钙硅比大于2.0时,β型硅酸二钙(Ca2SiO4,β-C2S)生成量随钙硅比的增大而增多;碳化0.5 h反应剧烈,抗压强度随钙硅比的增大先增加后降低,反应生成方解石、文石、球霰石。随着碳化反应延长至24 h,C3S2γ-C2S含量显著降低,方解石含量增长缓慢;C3S2降低了前期反应活性,但更持续的碳化反应和生成的多形态产物紧密交织,对后期抗压强度有提升作用,碳化24 h抗压强度和CO2吸收率分别为129.76 MPa、18.57%。

关键词: 钙硅比, 硅酸钙, 烧结行为, 固碳能力, 抗压强度

Abstract: Calcium silicate carbonatable binder is an important direction to realize the green and sustainable development of building materials industry. In order to study the effect of calcium silicon ratio (n(CaO)∶n(SiO2), molar ratio) on the composition of calcium silicate mineral phase and their carbon sequestration capabilities, calcium silicate carbonatable binders were synthesized with controlled calcium silicon ratio (n(CaO)∶n(SiO2)=1.8~2.2). Techniques such as t-pH, XRD, TGA, and SEM were employed to examine the evolution of phase composition, carbonization hardening process, CO2 uptakes and carbonization products of calcium silicate carbonatable binders. The results indicate that the content of γ-dicalcium silicate (Ca2SiO4, γ-C2S) initially increases and subsequently decreases as the calcium silicon ratio rises. When the calcium silicon ratio is no higher than 2.0, the content of rankinite (Ca3Si2O7, C3S2) gradually increases with the decreasing of calcium silicon ratio. When the calcium silicon ratio is higher than 2.0, the content of β-dicalcium silicate (Ca2SiO4, β-C2S) progressively increases with the increasing of calcium silicon ratio. The reaction of carbonization for 0.5 h is intense, and the compressive strength initial increases and subsequent decreases as the calcium silicon ratio increases. The reaction produces calcite, aragonite and vaterite. With the content of C3S2 and γ-C2S decreasing significantly, and the calcite content remains largely unchanged even when the carbonization reaction is extended to 24 h. C3S2 decelerates the early reaction of binder, but a more sustained carbonization reaction and a greater variety of carbonization products can enhance its subsequent compressive strength. The compressive strength and CO2 uptakes after carbonization for 24 h reach 129.76 MPa and 18.57%, respectively.

Key words: calcium silicon ratio, calcium silicate, sintering behavior, carbon sequestration capacity, compressive strength

中图分类号: