应用化学 ›› 2018, Vol. 35 ›› Issue (7): 802-811.DOI: 10.11944/j.issn.1000-0518.2018.07.170321

• 研究论文 • 上一篇    下一篇

阴离子交换树脂回收水相中有机磷酸萃取剂

苏文柔ab,陈继a*(),邓岳锋a,杨茂华a,刘川楹ab   

  1. a中国科学院长春应用化学研究所,稀土资源利用国家重点实验室 长春 130022
    b中国科学院大学 北京 100049
  • 收稿日期:2017-09-05 接受日期:2017-11-09 出版日期:2018-07-06 发布日期:2018-07-06
  • 通讯作者: 陈继
  • 基金资助:
    国家自然科学基金(51174184)项目资助

Recovery of Organphosphorus Extractants from Water by Anion Exchange Resin

Wenrou SUab,Ji CHENa*(),Yuefeng DENGa,Maohua YANGa,Chuanying LIUab   

  1. aState Key Laboratory of Rare Earth Resource Utilization,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun 130022,China
    bUniversity of Chinese Academy of Sciences,Beijing 100049,China
  • Received:2017-09-05 Accepted:2017-11-09 Published:2018-07-06 Online:2018-07-06
  • Contact: Ji CHEN
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.61106017)

摘要:

研究了阴离子交换树脂对水相中有机磷酸萃取剂的吸附。 通过比较不同的离子交换树脂对水相中2-乙基己基膦酸-单-2-乙基己基酯(P507)的去除率,发现大孔强碱性阴离子交换树脂(D201-OH)从水溶液中去除P507的能力最强,去除率可达99.24%。 而且当溶液在pH=1.0时,D201-OH对P507的吸附主要是分子吸附,其吸附等温线更适用于Langmuir模型;当溶液在pH=5.0时,阴离子交换反应占主导地位,其吸附等温线更适用于Freundlich模型。 研究还表明,D201-OH对P507的吸附在20 min内即达到吸附平衡时99.8%的吸附量。 通过动力学研究表明,拟一级动力学模型(R2>0.99)更适用于描述实验数据,并且吸附速率主要受膜扩散控制。 此外,吸附-解吸附循环8次后,D201-OH的吸附能力仍然保持在93%以上。 综上所述,D201-OH是有机磷酸类萃取剂的良好吸附剂,其吸附性能高效,循环过程稳定,因此可用于实际生产过程中回收有机磷酸萃取剂。

关键词: 阴离子交换树脂, 有机磷酸萃取剂, 吸附机理, 循环实验

Abstract:

The adsorption process of anion exchange resin to organphosphorus extractant in water was explored in this work. By comparing the removal of P507(2-ethylhexyl phosphoric acid mono-2-ethylhexyl ester) in water with different anion exchange resins, it is found that D201-OH(macroporous strong basic anion exchange resin) has the strongest ability to remove P507 from water, and the removal rate can reach to 99.24%. Secondly, at pH=1.0, the adsorption of P507 on D201-OH is mainly molecular adsorption and its adsorption isotherm is better fit to the Langmuir model; at pH=5.0, the anion exchange reaction is dominant and its adsorption isotherm is more suitable for the Freundlich model. Furthermore, the adsorption capacity of D201-OH to P507 reaches 99.8% of which in the adsorption equilibrium in 20 min. Kinetic study shows that the pseudo-first-order model(R2>0.99) exhibits a better fit to describe the experimental data and the adsorption rate may be controlled mainly by the film diffusion. Moreover, the adsorption capacity of D201-OH remains above 93% after eight cycles of adsorption-desorption. In summary, D201-OH is an excellent adsorbent for organphosphorus extractants with high stability in the repeated cycle. Therefore, it can be used to recover organphosphorus extractant in the practical production process.

Key words: anion exchange resin, organphosphorus extractant, adsorption mechanism, cycle experiment