Utilization of phosphogypsum to synthesize α-hemihydrate gypsum in H3PO4–H2O solution

磷石膏 石膏 半水合物 磷酸 X射线光电子能谱 Crystal(编程语言) 材料科学 晶种 核化学 晶体生长 化学工程 矿物学 冶金 化学 原材料 单晶 结晶学 工程类 有机化学 程序设计语言 计算机科学
作者
Long Chen,Lin Yang,Jianxin Cao
出处
期刊:Construction and Building Materials [Elsevier BV]
卷期号:368: 130453-130453 被引量:21
标识
DOI:10.1016/j.conbuildmat.2023.130453
摘要

Phosphogypsum (PG) is a kind of industrial solid waste with high impurity content and low utilization rate. In this study, α-hemihydrate gypsum (α-HH) was synthesized from PG in H3PO4–H2O solution (wet-process phosphoric acid solution and phosphoric acid solution) under atmospheric pressure. The crystal morphology of α-HH was controlled by adding F and Al compound regulators, and the mechanical properties of α-HH were improved. The difference of α-HH synthesized by PG with different qualities was analyzed, and the mechanism of α-HH morphology was studied by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and energy-dispersive spectroscopy (EDS). Results showed that in the wet-process phosphoric acid solution, α-HH synthesized from white PG (by H3PO4–H2SO4 two-step method) had better whiteness, purity, and mechanical properties compared with that from industrial PG, and the performance indexes of the α-HH products met the requirements of α50 grade in JC/T 2038–2010 α-high-strength gypsum in China and have a good commercial application prospect. Moreover, in the phosphoric acid solution, the average diameter of the α-HH crystal increased from 8.1 µm to 54.8 µm, the average aspect (L/D) ratio decreased from 32.65 to 0.52, and the induction period and growth period of the α-HH crystal were prolonged with the increase in regulator dosage. F− and Al3+ ions were preferred to adsorb on the crystal faces. The growth of the crystal parallel to c-axis (2 0 0), (0 2 0), and (4 0 0) was inhibited, and the morphology of the α-HH crystal changed from whisker to short column. When the dosage of the regulator was 1.1 %, the 2 h bending strength of the α-HH product was 6.56 MPa, and the drying compressive strength was 52.4 MPa. This study provides a new technique and method for the synthesis of high-strength α-HH products from PG.
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