首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Bioleaching mechanism of Co and Li from spent lithium-ion battery by the mixed culture of acidophilic sulfur-oxidizing and iron-oxidizing bacteria
【24h】

Bioleaching mechanism of Co and Li from spent lithium-ion battery by the mixed culture of acidophilic sulfur-oxidizing and iron-oxidizing bacteria

机译:嗜酸硫氧化铁氧化菌混合培养从废锂离子电池中浸出钴和锂的生物浸出机理

获取原文
获取原文并翻译 | 示例
       

摘要

The bioleaching mechanism of Co and Li from spent lithium-ion batteries by mixed culture of sulfur-oxidizing and iron-oxidizing bacteria was investigated. It was found that the highest release of Li occurred at the lowest pH of 1.54 with elemental sulfur as an energy source, the lowest occurred at the highest pH of 1.69 with FeS2. In contrast, the highest release of Co occurred at higher pH and varied ORP with S + FeS2, the lowest occurred at almost unchanged ORP with S. It is suggested that acid dissolution is the main mechanism for Li bioleaching independent of energy matters types, however, apart from acid dissolution, Fe2+ catalyzed reduction takes part in the bioleaching process as well. Co2+ was released by acid dissolution after insoluble Co3+ was reduced into soluble Co2+ by Fe2+ in both FeS2 and FeS2 + S systems. The proposed bioleaching mechanism mentioned above was confirmed by the further results obtained from the experiments of bioprocess-stimulated chemical leaching and from the changes in structure and component of bioleaching residues characterized by XPS, SEM and EDX.
机译:研究了硫和铁氧化细菌混合培养从废锂离子电池中提取钴和锂的生物浸出机理。发现以元素硫为能源,Li的最高释放发生在最低pH为1.54时,FeS2的释放最低发生在pH最高为1.69时。相比之下,Co的最高释放发生在较高的pH值下,并且随着S + FeS2的ORP发生变化,最低的发生在与S几乎不变的ORP下。这表明酸溶解是Li生物浸出的主要机理,与能量物质类型无关。除酸溶解外,Fe2 +催化的还原也参与了生物浸出过程。在FeS2和FeS2 + S系统中,Fe2 +将不溶性Co3 +还原为可溶Co2 +后,酸溶解释放Co2 +。从生物过程刺激的化学浸出实验以及以XPS,SEM和EDX表征的生物浸出残渣的结构和组分的变化获得的进一步结果证实了上述拟议的生物浸出机理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号