方解石
碳酸钙
化学
文石
三羧酸
缩放比例
Crystal(编程语言)
钙
无机化学
结晶学
矿物学
有机化学
柠檬酸循环
酶
程序设计语言
计算机科学
数学
几何学
作者
Yuwei Zuo,Yue Sun,Wenzhong Yang,Kegui Zhang,Yun Chen,Xingtian Yin,Ying Liu
标识
DOI:10.1016/j.molliq.2021.116093
摘要
The performance and mechanism of typical scaling inhibitors, i.e., 1-hydroxy ethylidene-1,1-diphosphonic acid (HEDP) and 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTCA), in inhibiting calcium carbonate scaling were investigated. Results of the static experiment at 30 °C and 80 °C revealed that at the optimal concentration, the scaling inhibition efficiency of PBTCA was superior to that of HEDP. Additionally, X-ray powder diffraction evaluation demonstrated that in comparison with HEDP, PBTCA inhibited the growth of the (1 0 4) crystal plane of calcite more evidently. Scanning electron microscopy analysis indicated that the addition of scaling inhibitors induced the crystal transformation of CaCO3 from calcite to aragonite. Molecular dynamics simulation also confirmed that the interaction of PBTCA with the (1 0 4) crystal surface of calcite is more apparent than that of HEDP. This observation was a consequence of the PBTCA being more negatively charged, as determined via a quantum chemical calculation. The calculation further indicated that the spatial distance of PBTCA to the (1 0 4) face of calcite was less due to stronger chelating ability and better suitability of the structure. As a result, in the tested temperature range, PBTCA exhibited the more effective inhibitory effect against calcium carbonate scaling.
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