4.5 Article

Adsorption Behavior of Iodine by Novel Covalent Organic Polymers Constructed Through Heterostructural Mixed Linkers

期刊

FRONTIERS IN MATERIALS
卷 6, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmats.2019.00012

关键词

covalent organic polymers; iodine; adsorption; kinetic analysis; thermodynamic analysis

资金

  1. National Natural Science Foundation of China [41572214, 41772241]
  2. Special Project of Jilin Provincial School Construction Project [SXGJXX2017-9]
  3. Graduate Innovation Fund of Jilin University
  4. 111 Project [B16020]

向作者/读者索取更多资源

The efficient capture and storage radioactive iodine (I-129 or I-131) formed during the extensive use of nuclear energy is of paramount importance. Therefore, it is a great deal to design and empolder new adsorbents for effectively disposing of iodine from nuclear waste. In this work, we presented a novel covalent organic polymer (JLUE-COP-3) constructed through heterostructural mixed linkers with perforated porousness, plenty of pi-conjugated phenyl rings and functional -CO-NH- and -SO3H groups to iodine adsorption process. After fully characterizing the morphology and structure, the adsorption behavior of iodine by the resultant polymers were explored in detail. The external adsorption behavior was determined to obey the pseudo-second order kinetic model according to the kinetic analysis. The maximum liquid adsorption capacity was obtained to reach 153.85 mg/g at 298 K, which was evaluated by the Langmuir isotherm model. In addition, the negative attributes of Delta G degrees as well as the positive attributes of Delta H degrees and Delta S degrees at three temperatures indicated the nature of the iodine adsorption over JLUE-COP-3 was spontaneous and endothermic. The current study could look forward to making great contributions to the facile fabrication of late-model three-component POP materials and their applications in treatment of nuclear waste.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据