Modeling the Kinetics of Saline Minerals Dissolution in Dombrovsky Quarry at the Kalush-Golinsky Potassium Salts Deposit

IF 0.5 Q4 MINERALOGY
Y. Malkova, V. Bobkov, V. Dolin
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引用次数: 0

Abstract

The article deals with the peculiarities of the chemical composition formation of brines in the Dombrovsky quarry, primarily due to the dissolution of potash ore minerals and host rocks in water coming from the pebble horizon and atmospheric precipitation. The solubility of the ore body minerals has been studied, and it ranges from 333 to 502 g∙dm–3. The boundary conditions for the formation of a saturated salt solution were determined. The estimated concentration of saturated potash ore solution under normal conditions is 426 g∙dm–3. The mechanism of dissolution is considered from the standpoint of D.I. Mendeleev's chemical theory of solutions. The temporary dynamics of minerals dissolution of the ore body is studied experimentally. The parameters of kinetic-diffusion process are calculated. The rate of the dissolution process, which occurs in the kinetic region, significantly exceeds the rate of concentration diffusion of hydrated ions: from 5 to 400 times depending on the mineral composition of salts. Theoretically from the point of view of multistage process kinetics and experimentally in laboratory conditions it is proved that the process that determines the formation of the chemical composition of brines (the slowest stage) is the concentration diffusion of hydrated ions Na+, K+, Cl–. They enter the liquid phase due to the minerals dissolution of the ore body and host rocks of soil and sides of the quarry, in the direction of overcoming the concentration difference - from the lower layers of the brine to its surface. This conclusion is confirmed by the ratio of weight coefficients а1 and а2. The contribution of the process of the main minerals dissolution of the ore body to the chemical composition formation of the solution is significantly less than the concentration diffusion process.
Kalush-Golinsky钾盐矿床Dombrovsky采石场盐矿溶解动力学模拟
本文讨论了东布罗夫斯基采石场卤水化学成分形成的特殊性,主要是由于来自卵石层和大气降水的水溶解了钾矿石矿物和承载岩。对矿体矿物溶解度进行了研究,其溶解度范围为333 ~ 502 g∙dm-3。确定了饱和盐溶液形成的边界条件。正常条件下饱和钾矿溶液的估计浓度为426 g∙dm-3。从门捷列夫溶液化学理论的观点出发,考察了溶解的机理。实验研究了矿体中矿物溶解的暂态动力学。计算了动力学扩散过程的参数。溶解过程发生在动力学区域,其速率明显超过水合离子的浓度扩散速率:根据盐的矿物组成,从5到400倍不等。从多阶段过程动力学的角度和实验室条件下的实验证明,决定卤水化学成分形成的过程(最慢的阶段)是水合离子Na+、K+、Cl -的浓度扩散。由于矿体、土壤和采石场两侧的宿主岩石的矿物溶解,它们进入液相,朝着克服浓度差异的方向-从盐水的下层到其表面。这一结论得到了权重系数比值(1和2)的证实。矿体主要矿物溶蚀过程对溶液化学成分形成的贡献明显小于浓度扩散过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
18
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