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基于MICP法的巴氏生孢八疊球菌固化鎘污染土的試驗研究

Experimental study on solidification of cadmium-contaminated soil by Sporosarcina pasteurii via MICP method

  • 摘要: 以重金屬污染土的治理為背景,通過毒性浸出、無側限抗壓強度、土柱淋濾試驗并結合鎘形態分析等其他微觀測試方法,探討了Ca2+的添加、Cd2+濃度、養護時間等因素對馴化巴氏生孢八疊球菌固化鎘污染土特性的影響. 結果表明:Ca2+對固化土中Cd2+浸出特性影響顯著,不添加Ca2+時,當尿素濃度為0.5 mol·L?1,固化土的Cd2+浸出質量濃度(0.42~5.64 mg·L?1)最低;添加Ca2+后,Cd2+浸出濃度略有增大,膠結液中尿素和Ca2+濃度均為0.5 mol·L?1時,Cd2+的固化效果較好. 延長養護時間,固化后土體的抗壓強度增加,Cd2+浸出濃度降低且固化效果提高;增大Cd2+濃度,固化后土體的抗壓強度降低,Cd2+浸出濃度提高;添加Ca2+有助于增強鎘污染土的固化效果,在養護時間為28 d時,當Cd2+濃度為100 mg·kg?1時,添加Ca2+的試樣強度達到312 kPa,相較于未添加Ca2+試樣強度(234 kPa)提升了33.3%;當Cd2+濃度增大至1600 mg·kg?1時,添加Ca2+的試樣強度達到269 kPa,相較于未添加Ca2+試樣強度提升了57.3%,試樣的浸出濃度降低了15.4%;經淋濾后,添加Ca2+的試樣濾出液中Cd2+濃度始終低于未添加Ca2+試樣. 固化后土中弱酸可提取態鎘向可還原態鎘和殘渣態鎘轉變,添加Ca2+進一步降低弱酸可提取態鎘所占比例,減小了Cd2+的遷移能力.

     

    Abstract: The immobilization of heavy metals using microbes presents an environmentally friendly approach, utilizing local indigenous microbes for remediating heavy metal-contaminated soils and improving soil environmental quality. Microbially induced carbonate precipitation (MICP), particularly through urea hydrolysis, is a typical biomineralization process in nature that has gained considerable attention. Sporosarcina pasteurii, a popular indigenous urease-producing bacterium, is especially effective in hydrolyzing urea. This study examines the effects of calcium ion (Ca2+) addition, cadmium ion (Cd2+) concentration, and curing time on the characteristics of cadmium-contaminated soil solidified by acclimatized Sporosarcina pasteurii. Various tests, including toxicity leaching, unconfined compressive strength, soil column leaching, cadmium speciation analysis, and microanalysis, were conducted to evaluate these effects. The results indicate that Ca2+ significantly affects the leaching behavior of Cd2+ in the contaminated soil after solidification. Without Ca2+, the lowest Cd2+ leaching concentration (0.42–5.64 mg·L?1) was observed at a urea concentration of 0.5 mol·L?1. When Ca2+ was added, the Cd2+ leaching concentration slightly increased, but optimal solidification efficiency was achieved when urea and Ca2+ concentrations were 0.5 mol·L?1. As curing time increased, the compressive strength of the solidified soil also improved, while Cd2+ leaching concentration decreased. The presence of Ca2+ further enhanced soil solidification over time. Higher Cd2+concentrations led to reduced compressive strength and increased leaching concentration. However, the addition of Ca2+ enhanced the solidification effect on cadmium-contaminated soil. At a curing time of 28 d, for a Cd2+ concentration of 100 mg·kg?1, the unconfined compressive strength of samples with Ca2+ reached 312 kPa, a 33.3% increase compared to 234 kPa without Ca2+. For a Cd2+ concentration of 1600 mg·kg?1, the unconfined compressive strength with Ca2+ reached 269 kPa, representing a 57.3% increase compared to samples without Ca2+, and the leaching concentration decreased by 15.4%. After leaching tests over 15 days using a geoenvironmental osmosis system revealed that the Cd2+ concentration in the leachate from samples with Ca2+ remained consistently lower than those without Ca2+. After solidification, weak acid-extracted cadmium in the contaminated soil transformed into reducible and residual forms. The addition of Ca2+ further reduced the proportion of weak acid-extractable cadmium, thereby reducing Cd2+ mobility. The calcium carbonate generated by the MICP reaction cements adjacent soil particles, thereby improving overall soil stability. Cadmium ions in the contaminated soil are immobilized by calcium carbonate through coprecipitation, forming stable compounds that reduce Cd2+ migration and bioavailability. This effectively alleviates soil heavy metal pollution. Overall, the results of this study will offer significant theoretical insight and technical innovations, holding profound implications for ecosystems, society, and the economy.

     

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