Effect of different retarders on setting time and mechanical properties of hemihydrate phosphogypsum-calcium sulfoaluminate cement composite binder

磷石膏 缓速器 材料科学 复合数 水泥 微观结构 石膏 结晶 复合材料 化学工程 化学 有机化学 原材料 工程类
作者
Zihao Jin,Liyue Wang,Ying Su,Xingyang He,Baoguo Ma,Yingbin Wang,Yubo Li,Huahui Qi,Bin Wang
出处
期刊:Construction and Building Materials [Elsevier BV]
卷期号:411: 134339-134339 被引量:10
标识
DOI:10.1016/j.conbuildmat.2023.134339
摘要

The optimization of mechanical properties and regulation in setting time of beta-hemihydrate phosphogypsum (β-HPG) are the key to its utilization in building materials. Calcium sulfoaluminate cement (SAC) can significantly enhance the mechanical properties of β-HPG to form a gypsum-based-composite binder, but have little effect on regulating the setting time. Retarders can regulate the setting time of β-HPG but decrease its mechanical properties. However, the synergistic modification mechanism of retarders and SAC on β-HPG has not been clarified. In this paper, the effects of protein retarder (SC) and citric acid (CA) on the setting time, hydration heat, mechanical properties and microstructure of the β-HPG-SAC composite binder were studied systematically. The results show that incorporating SC and CA can effectively regulate the setting time, but the effects on the mechanical properties differ. SC has a certain optimization effect on mechanical properties at low content, but has a negative effect when the content is over 0.2%, while CA has a continuous negative effect with its increasing content. Specifically, SC hinders the formation of the crystalline structure to a certain extent, and makes the crystallization of β-HPG and the hydration of SAC synergistic, while CA delays the hydration process of β-HPG and SAC simultaneously. Different from SC, CA can inhibit the growth of dihydrate gypsum (DH) crystals in the C-axis direction, transforming long rod crystals into short columns, eventually forming a looser microstructure and decreasing mechanical properties. This work provides an effective method for the modification of β-HPG and the high value-added resource utilization of PG.
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