Less-precious nitrogen-rich covalent organic frameworks capable of effective rare earth recovery from water

被引:15
|
作者
Zhang, Yi [1 ,2 ]
Liu, Donghao [1 ]
Guo, Weidong [1 ]
Ding, Yigang [1 ]
机构
[1] Wuhan Inst Technol, Engn Res Ctr Phosphorus Resources Dev & Utilizat, Sch Chem Engn & Pharm, Key Lab Green Chem Proc,Minist Educ,Hubei Key Lab, Wuhan 430073, Peoples R China
[2] China Univ Min & Technol, Key Lab Coal Proc & Efficient Utilizat, Minist Educ, Xuzhou 221008, Peoples R China
基金
中国国家自然科学基金;
关键词
Rare earth; COFs; Adsorption; Regeneration; Complexation interaction; PHOTOCATALYTIC HYDROGEN EVOLUTION; EFFICIENT REMOVAL; AQUEOUS-SOLUTION; ADSORPTION; ELEMENTS; SEPARATION; ADSORBENT; CATALYST; DESIGN; GROWTH;
D O I
10.1016/j.molliq.2023.121229
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of stable and inexpensive adsorbents for La(III) recovery from wastewater is of great importance for rare earth industries. In this work, two novel N-rich covalent organic frameworks (COFs) synthesized via a one-step solvothermal method were termed as COF-PA-CC and COF-ML-CC, and employed as the adsorbents for removal of rare earth (RE) ions from aqueous solution. The structures and properties of COFs were characterized with X-ray diffractometer, total reflection infrared spectrom-eter, field-emission scanning electron microscopy, X-ray photoelectron spectroscopy, nitrogen adsorp-tion-desorption instrument and thermogravimetric analyzer. The results revealed that COF-PA-CC composed of nanowires with the average length of 500 nm, whereas COF-ML-CC displayed the spherical morphology with the diameter of 100 ti 300 nm. Specific surface areas of COF-PA-CC and COF-ML-CC were calculated to be 82.13 and 191.08 m2/g, respectively. The adsorption process of La(III) was well -fitted with pseudo-second-order kinetic model and Langmuir isotherm model, exhibiting the high adsorption capacities of 150.88 and 168.19 mg/g for COF-PA-CC and COF-ML-CC after 120 min. Moreover, the influences of pH, temperature, different RE ions on adsorption performances were compre-hensively tested, yielding an optimal adsorption condition (pH = 5.5, 65 degrees C and 120 min) and a better affinity for some light RE ions. Importantly, the fabricated COFs possess the excellent reusability after five adsorption-regeneration cycles, remaining 97.84 % and 95.51 % of initial capacities for COF-PA-CC and COF-ML-CC, respectively. The adsorption mechanism revealed that the complexation interaction between La(III) and the unoccupied N sites of N-rich COFs was recommended to interpret the remarkable adsorp-tion performance of La(III) on the basis of the characterization analysis after the adsorption with elemen-tal mapping, EDS and XPS. Consequently, these low-cost and robust COFs with abundant active N sites supplied a promising strategy for the recovery of RE ions from wastewater. (c) 2023 Elsevier B.V. All rights reserved.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Stable nitrogen-containing covalent organic framework as porous adsorbent for effective iodine capture from water
    Chen, Run
    Hu, Tianliang
    Li, Yongqiang
    REACTIVE & FUNCTIONAL POLYMERS, 2021, 159
  • [42] Novel benzylphosphate-based covalent porous organic polymers for the effective capture of rare earth elements from aqueous solutions
    Ravi, Seenu
    Kim, Seo-Yul
    Bae, Youn-Sang
    JOURNAL OF HAZARDOUS MATERIALS, 2022, 424
  • [43] Protonated covalent organic frameworks for green and effective recovery of Au(I) from thiosulfate solutions: Performance, DFT calculations, and mechanism insights
    Xiong, Jiaxing
    Zhou, Yu
    Ren, Boxian
    Zhang, Zichen
    Zhang, Yuan
    Zhang, Jing
    Chang, Jun
    Yang, Xiangjun
    Wang, Shixiong
    SEPARATION AND PURIFICATION TECHNOLOGY, 2025, 353
  • [44] Ultrafast Selective Enrichment of Ammonia Nitrogen from Water Using Sulfonated Covalent Organic Frameworks Bearing Single Cu Sites
    Jin, Wei
    Liu, Jinglin
    Huang, Naixian
    Wang, Zihao
    Zhang, Yunhui
    Peng, Yongwu
    Gong, Chengtao
    Ok, Yong Sik
    Xu, Zuxin
    ACS ES&T ENGINEERING, 2023, 3 (10): : 1511 - 1520
  • [45] Effective extraction and detection of aflatoxins in cereals using nitrogen-rich benzodiimidazole linkage magnetic covalent organic framework based solid phase extraction and HPLC-MS/MS analysis
    Wei, Dan
    Li, Jianliang
    Zheng, Shuangshuang
    Guo, Ming
    Xu, Jingjing
    Deng, Qiao
    Wang, Xu
    FOOD CHEMISTRY-X, 2024, 24
  • [46] Cu-N4 single atoms derived from metal-organic frameworks with trapped nitrogen-rich molecules and their use as efficient electrocatalysts for oxygen reduction reaction
    Lu, Fenghong
    Fan, Kaicai
    Cui, Lixiu
    Yang, Ye
    Wang, Wenxuan
    Zhang, Guitao
    Wang, Chengbin
    Zhang, Qi
    Li, Bin
    Zong, Lingbo
    Wang, Lei
    CHEMICAL ENGINEERING JOURNAL, 2022, 431
  • [47] Recovery of rare earth elements from sulfate-rich acid mine water: Looking through the keyhole the exchange reaction for cationic resin
    Silva, Gabriela Cordeiro
    Bertoli, Alexandre Carvalho
    Duarte, Helio Anderson
    Ladeira, Ana Claudia Queiroz
    JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING, 2022, 10 (06):
  • [48] Enhanced & effective phosphate recovery from water by indium fumarate & zirconium fumarate metal-organic frameworks: Synthesis, characterization, adsorption, kinetic and isotherm studies
    Ozcelik, Gulsum
    Cavusoglu, Ferda Civan
    Ozkara-Aydinoglu, Seyma
    Bayazit, Sahika Sena
    SURFACES AND INTERFACES, 2022, 29
  • [49] Effective strategies toward imine-linked cationic covalent organic frameworks for rapid and selective removal of 99TcO4- from water: insights from DFT and MD calculations
    Zhao, Chaofeng
    Ma, Xinjie
    Wei, Xin
    Liu, Weiwei
    Sun, Lu
    Ai, Yuejie
    ENVIRONMENTAL SCIENCE-NANO, 2023, 10 (02) : 611 - 624
  • [50] A rational design and green synthesis of 3D metal organic frameworks containing a rigid heterocyclic nitrogen-rich dicarboxylate: structural diversity, CO2 sorption and selective sensing of 2,4,6-TNP in water
    Gogia, Alisha
    Mandal, Sanjay K.
    DALTON TRANSACTIONS, 2019, 48 (07) : 2388 - 2398