Fredd CN, Fogler HS
Department of Chemical Engineering, University of Michigan, 2300 Hayward Street, Ann Arbor, Michigan, 48109
J Colloid Interface Sci. 1998 Aug 1;204(1):187-97. doi: 10.1006/jcis.1998.5535.
The kinetics of calcite dissolution in the presence of calcium chelating agents was investigated over the pH range of 3.3-12 using a rotating disk apparatus. The results show that the rate of dissolution is increased significantly by the presence of chelating agents such as CDTA, DTPA, and EDTA. The rate of dissolution is influenced by the kinetics of the chelation reactions and varies considerably with pH and type of chelating agent. A surface chelation mechanism was introduced to describe the dissolution. The mechanism involves the adsorption of the chelating agent onto the calcite surface and follows Langmuir-Hinshelwood kinetics. The dissolution is different from conventional hydrogen ion attack in that the chelating agent attacks the calcium component of the lattice rather than the carbonate component. Therefore, the rate of dissolution is enhanced by the influence of hydrogen ion attack at low pH. In addition, the various ionic forms of the chelating agents react with the calcite surface at different rates depending on the number of hydrogen ions associated with the species. In general, the rate of dissolution increases with increasing protonation. The surface complexation mechanism was shown to describe the rate of calcite dissolution in the presence of chelating agents over the pH range of 4-12. Copyright 1998 Academic Press.
使用旋转圆盘装置,在pH值为3.3 - 12的范围内研究了方解石在钙螯合剂存在下的溶解动力学。结果表明,CDTA、DTPA和EDTA等螯合剂的存在显著提高了溶解速率。溶解速率受螯合反应动力学影响,并且随pH值和螯合剂类型的不同而有很大变化。引入了一种表面螯合机制来描述溶解过程。该机制涉及螯合剂在方解石表面的吸附,并遵循朗缪尔 - 欣谢尔伍德动力学。这种溶解与传统的氢离子侵蚀不同,因为螯合剂攻击的是晶格中的钙成分而非碳酸盐成分。因此,在低pH值下,氢离子侵蚀的影响会提高溶解速率。此外,螯合剂的各种离子形式根据与该物种相关的氢离子数量以不同速率与方解石表面反应。一般来说,溶解速率随着质子化程度的增加而提高。表面络合机制被证明可以描述在pH值为4 - 12的范围内,螯合剂存在下方解石的溶解速率。版权所有1998年学术出版社。