Comparison of the efficiency of traditional MICP and two-step MICP method for immobilizing heavy metals in aquatic environments

Xiaosong Huang , Rongjun Zhang , Junjie Zheng
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Abstract

The application of the microbially induced carbonate precipitation (MICP) method for remediating heavy metals (i.e., HMs) has recently garnered significant attention. Nevertheless, the inhibition of urease activity by toxic Cd2+, Pb2+, Zn2+, and Cu2+ poses a challenge for MICP-based remediation of HMs contamination. This study: (1) first performed the traditional MICP tests (in which the bacterial solution, urea solution, and HMs were mixed simultaneously), and investigated the toxic effect of HMs on the urease activity and the immobilization efficiency, (2) analyzed the toxicity and immobilization mechanism during the MICP process by combining the simulation and XRD tests, (3) conducted the two-step MICP tests (which initially mixed the bacterial solution and urea solution to promote urea hydrolysis, then added the HMs solutions for HMs precipitation) to improve the immobilization efficiency. The tube experiments and simulations were investigated in the HMs concentration range from 1 to 10 mmol/L. Indicators including ammonium concentration, HMs concentrations, and pH were measured/recorded during the tests. The results show that soluble HMs exhibit a concentration-dependent inhibition of urea hydrolysis during the traditional MICP process, resulting in a decreasing immobilization efficiency. The two-step MICP method can effectively immobilize almost the Cd2+ and Zn2+ when the initial urea hydrolysis period exceeds 1–2 h. In addition, a high immobilization rate of over 90% can be achieved for Cu-contaminated solutions at the optimal first-step reaction time. Compared with the traditional MICP procedure, the effective two-step MICP method exhibits more promising application prospects for the immobilization of soluble HMs in aquatic environments.
传统MICP法与两步MICP法固定化水中重金属的效果比较
应用微生物诱导碳酸盐沉淀(MICP)方法修复重金属(即HMs)最近引起了极大的关注。然而,毒性Cd2+、Pb2+、Zn2+和Cu2+对脲酶活性的抑制对基于micp的HMs污染修复提出了挑战。本研究:(1)首先进行传统的MICP试验(细菌溶液、尿素溶液和HMs同时混合),考察HMs对脲酶活性和固定化效率的毒性作用;(2)通过模拟和XRD试验相结合,分析MICP过程中的毒性和固定化机制;(3)进行两步MICP试验(首先将细菌溶液和尿素溶液混合,促进尿素水解;然后加入HMs溶液进行HMs沉淀),提高固定化效率。在1 ~ 10 mmol/L的HMs浓度范围内进行了试管实验和模拟。在试验期间测量/记录铵浓度、HMs浓度和pH等指标。结果表明,在传统的MICP工艺中,可溶性HMs对尿素水解的抑制作用呈浓度依赖性,导致固定化效率降低。当初始尿素水解时间超过1 ~ 2 h时,两步MICP法几乎可以有效地固定Cd2+和Zn2+,并且在最佳的第一步反应时间下,cu污染溶液的固定率可以达到90%以上。与传统的MICP方法相比,有效的两步MICP方法在水生环境中固定化可溶性HMs具有更广阔的应用前景。
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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