首页> 外文期刊>Environmental Science and Pollution Research >Characteristics and mechanisms of nickel adsorption on biochars produced from wheat straw pellets and rice husk
【24h】

Characteristics and mechanisms of nickel adsorption on biochars produced from wheat straw pellets and rice husk

机译:小麦秸秆颗粒和稻壳生产的镍吸附的特性和机制

获取原文
获取原文并翻译 | 示例
           

摘要

The adsorption characteristics and mechanisms of Ni2+ on four-standard biochars produced from wheat straw pellets (WSP550, WSP700) and rice husk (RH550, RH700) at 550 and 700 A degrees C, respectively, were investigated. The kinetic results show that the adsorption of Ni2+ on the biochars reached an equilibrium within 5 min. The increase of the solid to liquid ratio resulted in an increase of Ni2+ removal percentage but a decrease of the adsorbed amount of Ni2+ per weight unit of biochar. The Ni2+ removal percentage increased with the increasing of initial solution pH values at the range of 2-4, was relatively constant at the pH range of 4-8, and significantly increased to ae98% at pH 9 and stayed constantly at the pH range of 9-10. The calculated maximum adsorption capacities of Ni2+ for the biochars follow the order of WSP700 > WSP550 > RH700 > RH550. Both cation exchange capacity and pH of biochar can be a good indicator of the maximum adsorption capacity for Ni2+ showing a positively linear and exponential relationship, respectively. This study also suggests that a carefully controlled standardised production procedure can make it reliable to compare the adsorption capacities between different biochars and investigate the mechanisms involved.
机译:研究了Ni2 +对小麦秸秆粒粒子(WSP550,WSP700)和稻壳(RH550,RH700)产生的四标准生物脉冲的吸附特性和机制,分别在550和700℃下进行。动力学结果表明,在5分钟内,Bi2 +对Biochars的吸附达到平衡。液体比的升高导致Ni2 +去除率的增加,但在Biochar的每重量单位的Ni2 +的吸附量的降低。 Ni2 +去除百分比随着初始溶液pH值的增加而增加,在2-4的温度范围内相对恒定,在4-8的pH范围内,并且在pH 9的AE 98%显着增加并保持不变pH范围为9-10。 Ni2 +的用于生物炭的计算出的最大吸附容量按照WSP700> WSP550> RH700> RH550的顺序。阳离子交换能力和生物炭的pH可以是Ni2 +的最大吸附能力的良好指标,分别显示出积极的线性和指数关系。本研究还表明,精心控制的标准化生产程序可以使其可靠地比较不同生物触发器之间的吸附能力并调查所涉及的机制。

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