Graphene oxide modified H4L-ion imprinting electrochemical sensor for the detection of uranyl ions

被引:8
作者
Li, Yujie [1 ]
Wang, Zhimei [1 ]
Liu, Chen [2 ]
Zhang, Di [2 ]
Liao, Lifu [2 ]
Xiao, Xilin [1 ,2 ,3 ]
机构
[1] Univ South China, Coll Resource & Environm & Safety Engn, Hengyang City 421001, Peoples R China
[2] Univ South China, Coll Chem & Chem Engn, Hunan Prov Key Lab Typical Environm Pollut & Hlth, Hengyang City 421001, Peoples R China
[3] Hunan Univ, State Key Lab Chemo & Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
来源
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE | 2021年 / 647卷 / 19期
基金
中国国家自然科学基金;
关键词
Electrochemistry; Trace analysis; Uranyl ions; Ion-imprinting; Graphene oxide; CARBON; RECOGNITION; POLYMERS; URANIUM; PRECONCENTRATION; NANOPARTICLES; ELECTRODES; THORIUM;
D O I
10.1002/zaac.202100182
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The rapid development of the nuclear industry has gradually aroused people ' s attention to the problem of nuclear pollution. Due to the biological toxicity of uranium and its aqueous solution, simple and rapid detection of uranium in the water environment is quite important. An ion imprinted carbon nanomaterial (graphene oxide) electrochemical sensor for the detection of trace uranyl ions was prepared by using the synthesized bipolar tetradentate macrocyclic uranyl ligand cyclo-bis-phenylenediamine-bis-(phenylmethyl-diphyrrolecarbaldehyde) (H4L) as functional monomer. The sol-gel polymer was prepared by hydrolysis and polymerization of H4L ligand, 3-aminopropyltrimethoxysilane and tetraethoxysilane. H4L-ion imprinted polymer (U-IIP) was prepared by adding 1 mM uranyl ion as template ions. Then the polymer was bonded to graphene oxide modified carbon paste electrode, and the template ions were eluted to obtain H4L-ion imprinted-graphene oxide modified carbon paste electrode (U-IIP/GO/CPE). Differential pulse voltammetry was used to detect trace uranyl ions. The results showed that the U-IIP/GO/CPE sensor system can detect uranyl ions with high sensitivity and specificity, and the peak current appeared around -0.26v. In the range of 0.01 mu M similar to 3.0 mu M, the detection current had a good linear relationship with the molar concentration of uranyl ions, and the method detection limit was 1.32 nM (S/N=3). Through the detection of actual samples, it had a good acceptable recovery rate (95.45 %similar to 106.25 %), and the relative standard deviation was less than 3.25 %.
引用
收藏
页码:1914 / 1920
页数:7
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