负载亚铁氰化钴钾废弃皮革吸附剂对Rb(I)的吸附
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TQ 028.3

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国家国防基础科研计划项目(16ZG6101) ;国家自然科学基金(21406182);西南科技大学研究生创新基金(17ycx006)


Adsorption of Rb (Ⅰ) with Potassium Cobalt Ferrocyanide Loaded on Waste Leather
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the Nuclear Energy Special Project (13zg610301); the National Natural Science Foundation of China (21406182).

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    摘要:

    将亚铁氰化钴钾负载于经碱水解后的废弃皮革上,制备了一种铷离子吸附剂。采用扫描电子显微镜(SEM)、傅里叶变换红外光谱(FT-IR)、X-射线光电子能谱(XPS)和X-射线衍射(XRD)等对其进行了表征。考察了Co(NO3)2•6H2O和K4Fe(CN)6•3H2O的质量比、溶液pH、铷离子(Rb+)初始质量浓度、吸附剂用量和接触时间对吸附效果的影响。结果表明:m〔Co(NO3)2•6H2O〕:m〔K4Fe(CN)6•3H2O〕=3:4时,制备的0.09 g吸附剂对pH为7、初始质量浓度为20 mg/L 的Rb+溶液的吸附率为93.55% ,且于6 h达吸附平衡。探究发现,Langmuir等温吸附模型和准二级动力学模型能更好地描述Rb+在吸附剂上的吸附行为。以1.5 mol/L KCl作为脱附剂,脱附率达90%以上。将该吸附剂用于提取盐湖卤水中的Rb+,当pH=7时,吸附率为51.19%,该吸附剂具有潜在的实用价值。

    Abstract:

    otassium cobalt ferrocyanide was loaded on alkali-hydrolyzed waste leather to prepare a kind of adsorbent for Rb+ adsorption, whose structure and morphology were characterized with scan electron microscope (SEM), fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD). The effects of the mass ratio of Co(NO3)2•6H2O and K4Fe(CN)6•3H2O, pH, initial Rb+ mass concentration, adsorbent dosage, and contact time on adsorption capacity of adsorbent for Rb+ were investigated. The results showed that the adsorbent presented higher adsorption capacity for Rb+ when the mass ratio was 3:4. The adsorption efficiency was 93.55% at pH 7, adsorbent dosage of 0.09 g and initial Rb+ mass concentration of 20 mg/L, and adsorption achieved equilibrium at 6 h. The isothermal and kinetics of Rb+ adsorption on KCoFC-AWL were fitted well with Langmuir isotherm model and pseudo-second-order kinetics model. Up to 90% desorption efficiency of Rb+ was achieved with 1.5 mol/L KCl. The adsorption efficiency reached up to 51.19% when the adsorbent was utilised to adsorb Rb+ from saline lake at pH 7, indicating its potential application advantages as an efficient adsorbent.

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杨嘉怡,罗学刚,周建,杨素秋.负载亚铁氰化钴钾废弃皮革吸附剂对Rb(I)的吸附[J].精细化工,2018,35(3):

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  • 收稿日期:2017-04-19
  • 最后修改日期:2017-07-09
  • 录用日期:2017-08-04
  • 在线发布日期: 2018-03-15
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