Zhang Donghua, Liu Zhimeng
Department of Mining Engineering, College of Mining Engineering, Taiyuan University of Technology, Taiyuan, 030024, China.
Shanxi Coal Institute of Planing &design (group) Co.,ltd., Taiyuan, 030024, China.
Heliyon. 2024 Jul 17;10(15):e34664. doi: 10.1016/j.heliyon.2024.e34664. eCollection 2024 Aug 15.
Layered double hydroxides (LDH-D) and their calcined counterparts, using dolomite as a source of magnesium, were utilized for the immobilization of chromium (Cr(VI)) in soil. The results indicate that LDH-D, both with and without varying calcination temperatures, can effectively immobilize Cr(VI) in soil. Among the different calcination temperatures tested, LDH-D subjected to calcination at 500 °C (LDH-D-500) showed particularly high efficacy. Long-term TCLP experiments demonstrated the inhibition of soil-to-plant transmission of Cr(VI), thereby highlighting the long-lasting immobilization capacity of LDH-D and its calcined derivatives. Furthermore, the analysis of the microbial community's adaptation in post-remediation soil confirmed the durability and bioavailability of LDH-D-500 for Cr immobilization. Examination of the material's morphology and structure after immobilization shed light on the mechanism of immobilization in soil. The results revealed that interlayer anion exchange and surface adsorption were the main factors responsible for the effective immobilization of LDH-D and LDH-D-300. On the other hand, LDH-D-900, with a dominant spinel (MgAlO) structure, faced challenges in returning to its original layered configuration, making surface adsorption the primary mechanism for immobilization. LDH-D-500 primarily relied on the structure memory effects of LDHs to immobilize Cr(VI) through structural recovery processes, facilitated by electrostatic attraction and surface adsorption. It is also important to note that CaCO plays an important role in adsorption. Additionally, a portion of Cr(VI) was converted to Cr(III) through phenomena such as isomer substitution and complexation adsorption. The proficiency of LDH-D-500 in immobilizing Cr, its ability for instantaneous separation, and the potential for regeneration make it a promising material for remediation of heavy metal-contaminated soil. The investigations suggest that the use of dolomite to create hydrotalcite and calcining it at 500 °C could effectively render environmental Cr inactive, thereby optimizing resource utilization.
以白云石为镁源的层状双氢氧化物(LDH-D)及其煅烧产物被用于固定土壤中的铬(Cr(VI))。结果表明,无论是否经过不同的煅烧温度处理,LDH-D都能有效地固定土壤中的Cr(VI)。在所测试的不同煅烧温度中,在500℃煅烧的LDH-D(LDH-D-500)表现出特别高的效率。长期的TCLP实验证明了对Cr(VI)从土壤到植物传输的抑制作用,从而突出了LDH-D及其煅烧衍生物的持久固定能力。此外,对修复后土壤中微生物群落适应性的分析证实了LDH-D-500对Cr固定的耐久性和生物有效性。固定后对材料形态和结构的检查揭示了土壤中固定的机制。结果表明,层间阴离子交换和表面吸附是LDH-D和LDH-D-300有效固定的主要因素。另一方面,具有主要尖晶石(MgAlO)结构的LDH-D-900在恢复其原始层状结构方面面临挑战,使得表面吸附成为固定的主要机制。LDH-D-500主要依靠层状双氢氧化物的结构记忆效应,通过结构恢复过程固定Cr(VI),这一过程由静电吸引和表面吸附促进。还需要注意的是,CaCO在吸附中起重要作用。此外,一部分Cr(VI)通过异构取代和络合吸附等现象转化为Cr(III)。LDH-D-500在固定Cr方面的熟练程度、其即时分离能力和再生潜力使其成为修复重金属污染土壤的有前途的材料。研究表明,利用白云石制备水滑石并在500℃煅烧可以有效地使环境中的Cr失活,从而优化资源利用。