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紫硫细菌对氯铂酸配合物的生物去除。

Bio-removal of PtCl complex by Galdieria sulphuraria.

机构信息

School of Chemistry & Chemical Engineering, Anhui University, Jiulong Rd 111, Hefei, Anhui 230039, PR China; Key Laboratory of Structure and Functional Regulation of Hybrid Materials (Anhui University), Ministry of Education, Hefei, Anhui 230601, PR China.

School of Chemistry & Chemical Engineering, Anhui University, Jiulong Rd 111, Hefei, Anhui 230039, PR China.

出版信息

Sci Total Environ. 2021 Nov 20;796:149021. doi: 10.1016/j.scitotenv.2021.149021. Epub 2021 Jul 12.

Abstract

Bio-removal of negative charged platinum complex is of great challenge owing to electrostatic repulsions between PtCl and general extracellular polymeric substance (EPS) of microorganism. Galdieria sulphuraria (GS) are thermophilic and acidophilic microalga with specific metabolism, which subsequently lead to their unique cellular compositions such as EPS and phycocyanin, possibly providing a strategy to deal with negative charged metal complex. Accordingly, G. sulphuraria are employed to remove negative charged PtCl complex with initial concentrations ranging from 0, 10, 20, 30, to 45 ppm. The growth rates of G. sulphuraria with microalgae named as GS-0, GS-10, GS-20, GS-30, and GS-45, respectively, and simultaneously bio-removal efficiencies of PtCl are investigated. G. sulphuraria are independent to PtCl within 0-30 ppm, while they are inhibited within 45 ppm of PtCl. The PtCl removal efficiencies of GS-10, GS-20, and GS-30 increase from 94.58%, 95.52%, to 95.92%, while decrease to 71.81% of GS-45. About 92.39%, 93.77%, 94.29%, and 75.21% of PtCl adsorbed are accumulated within GS-10, GS-20, GS-30, GS-45, with few in EPS. The PtCl complexes accumulated in EPS and algae cells are possibly decomposed to PtCl according to the increasing zeta potentials of EPS and algae cells. The results indicate that PtCl is efficiently removed by G. sulphuraria, achieving bio-removal of negative charged PtCl complex from wastewater.

摘要

由于 PtCl 与微生物一般细胞外聚合物 (EPS) 之间的静电排斥,带负电荷的铂络合物的生物去除极具挑战性。硫氧还蛋白(GS)是一种嗜热嗜酸微藻,具有特殊的代谢途径,这导致其独特的细胞组成,如 EPS 和藻蓝蛋白,这可能为处理带负电荷的金属络合物提供了一种策略。因此,使用硫氧还蛋白来去除初始浓度范围为 0、10、20、30 和 45ppm 的带负电荷的 PtCl 络合物。研究了分别命名为 GS-0、GS-10、GS-20、GS-30 和 GS-45 的微藻 GS 中硫氧还蛋白的生长速率和 PtCl 的生物去除效率。在 0-30ppm 范围内,硫氧还蛋白独立于 PtCl,而在 45ppm 的 PtCl 范围内,硫氧还蛋白受到抑制。GS-10、GS-20 和 GS-30 的 PtCl 去除效率从 94.58%、95.52%增加到 95.92%,而 GS-45 的 PtCl 去除效率则下降到 71.81%。大约 92.39%、93.77%、94.29%和 75.21%的 PtCl 吸附量分别在 GS-10、GS-20、GS-30 和 GS-45 中积累,而在 EPS 中积累较少。根据 EPS 和藻类细胞的zeta 电位增加,推测在 EPS 和藻类细胞中积累的 PtCl 络合物可能分解为 PtCl。结果表明,硫氧还蛋白能够有效地去除 PtCl,从而实现从废水中去除带负电荷的 PtCl 络合物。

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