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L-组氨酸-赤藓红复合膜修饰电极同时检测对苯二酚、邻苯二酚 被引量:8

Simultaneous Determination of Hydroquinone and Catechol Based on L-Histidine-Erythrosine Composite Film Modified Glassy Carbon Electrode
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摘要 利用循环伏安法制备了L-组氨酸-赤藓红复合膜修饰玻碳电极(L-His-Erythrosine/GCE).采用扫描电镜(SEM)观察修饰电极的表面形貌结构,并用电化学阻抗谱(EIS)、循环伏安法(CV)表征修饰电极的电化学性能.在此基础上用差分脉冲伏安法(DPV)研究了对苯二酚(HQ)和邻苯二酚(CC)混合物在该电极上的电催化氧化,结果表明,L-His-Erythrosine/GCE对HQ及CC的电化学氧化具有显著的催化作用,两种异构体在该修饰电极上的氧化过电位明显降低,峰电流显著增大,二者氧化峰电位间隔达108mV,表明制备的修饰电极可用于HQ和CC的同时检测.在最佳实验条件下,HQ与CC浓度在1.2×10^-6~1.1×10^-4mol·L^-1范围内与氧化峰电流呈良好线性关系,检出限分别为0.19μmol·L^-1(HQ)和0.16μmol·L^-1(CC)(S/N=3).另外,此修饰电极具有较好的重现性和较强的抗干扰能力,将修饰电极用于实际水样品中HQ和CC的测定,其加标回收率分别为99.9%~100.6%(HQ)、99.2%~100.2%(CC). By using cyclic voltammetry method, L-histidine and erythrosine was electrodeposited on the surface of glassy carbon electrode (GCE) to obtain the modified electrode (denoted as L-His-Erythrosine/GCE). The morphology of L-His-Erythrosine/GCE was characterized by scanning electron microscopy (SEM) , and the electrochemical property characterization of L-His-Erythrosine/ GCE was investigated using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) techniques. The electroeatalytie oxidation of bydroquinone (HQ) and eateehol (CC) on the modified electrode was discussed by differential pulse vohammetry (DPV) in this study. The L-His-Erythrosine/GCE had shown an excellent electroeatalytie activity for HQ and CC. The oxidation overpotentials of HQ and CC decreased significantly and the corresponding oxidation currents increased remarkably. Due to the large separation of oxidation peak potentials ( 108 mV) , concentrations of HQ and CC can be easily determined simultaneously. Under the optimum conditions, the oxidation peak currents for both HQ and CC increased linearly with the respective concentrations in the 1.2 × 10^-6 to 1. 1 × 10^-4mol·L^-1 concentration range, with the detection limits of 0. 19 and 0. 16 μmol·L^-1 (S/N = 3) , respectively. Furthermore, the modified electrode exhibited good reproducibility and selectivity. The modified electrode was successfully applied to the simultaneous determination of HQ and CC in actual water samples, the recoveries got by standard addition method were in ranges of 99.9% -100.6% (HQ) and 99.2% -100.2% (CC).
出处 《环境科学》 EI CAS CSCD 北大核心 2015年第4期1365-1373,共9页 Environmental Science
基金 国家自然科学基金项目(41101223) 重庆市教育委员会项目(KJ131205 KJ131203) 重庆市永川区科委项目(Ycstc 2013nc8001) 重庆文理学院重点项目(Z2013CH16)
关键词 L-组氨酸 赤藓红 修饰电极 邻苯二酚 对苯二酚 L-histidine erythrosine modified electrodes hydroquinone catechol
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参考文献39

  • 1Huang K J, Wang L, Liu Y J, et al. Synthesis and electrochemical performances of layered tungsten sulfide-graphene nanocomposite as a sensing platform for catechol, resorcinol and hydrnquinone [ J ]. Electrochimica Acta, 2013, 107 : 379- 387.
  • 2Feng X, Gao W W, Zhou S H, et al. Discrimination and simultaneous determination of hydroquinone and catechol by tunable polymerization of imidazolium-based ionic liquid on multi- walled carbon nanotube surfaces [ J]. Analytiea Chimica Aeta, 2013, 805: 36-44.
  • 3Xin H S, Zhang Q M, Zhou Y L, et al. Electrochemical behavior of eatechol, resoreinol and hydroquinone at grapheme- chitosan composite film modified glassy carbon electrode and their simultaneous determination in water samples [J]. Eleetrochimica Aeta, 2011, 56(6) : 2748-2753.
  • 4Chen X, Parker S G, Zou G, et al. β-Cyclodextrin- funetionafized silver nanoparticles for the naked eye detection of aromatic isomers [ J]. ACS Nano, 2010, 4( 11 ) : 6387-6394.
  • 5Gao W H, Cristina L Q. Fast and sensitive high performance liquid chromatography analysis of cosmetic creams for hydroquinone, phenol and six preservatives [ J ]. Journal of Chromatography A, 2011, 1218(28):4307-4311.
  • 6Wang H Y, Chen D L, Wei Y J, et al. A localized surface plasmon resonance light scattering-based sensing of hydroquinone via the formed silver nanoparticles in system [ J]. Speetroehimiea Acta Part A, 2011 , 79(5) : 2012-2016.
  • 7Li S F, Li X Z, Xu J, et al. Flow-injection chemiluminescence determination of polyphenols using luminal-NalO4 -gold nanoparticles system[J]. Talanta, 2008, 75(1): 32-37.
  • 8Sirajuddin, Bhanger M I, Niaz A, et al. Uhra-trace level determination of hydroquinone in waste photographic solutions byUV-vis spectrophotometry [ J ]. Talanta, 2007, 72 ( 2 ) : 546- 553.
  • 9Judefeind A, Rensburg P J, Langelaar S, et al. Stable isotope dilution analysis of salicylic acid and hydroquinone in human skin samples by gas chromatography with mass spectrometric detection[J]. Journal of Chromatography B, 2007, 852(1-2) : 300-307.
  • 10Dong S Q, Chi L Z, Yang Z Y, et al. Simultaneous determination of dihydroxybenzene and phenylenediamine positional isomers using capillary zone electrophoresis coupled with amperometric detection [ J]. Journal of Separation Science, 2009, 32(18) : 3232-3238.

二级参考文献64

  • 1吕鹏,史建国,冯东,庄重,王建传,凌建亚,张长铠.邻苯二酚双加氧酶传感器的研究[J].中国环境科学,2005,25(4):491-493. 被引量:4
  • 2李明齐,何晓英,蔡铎昌.碳纳米管修饰电极对对苯二酚和邻苯二酚的电催化研究[J].分析科学学报,2006,22(3):299-302. 被引量:25
  • 3张英,袁若,柴雅琴,傅英姿,卓颖,黎雪莲,朱强,王娜.纳米金修饰玻碳电极测定邻苯二酚[J].理化检验(化学分册),2007,43(6):468-471. 被引量:10
  • 4Tang L, Zeng G M, Liu J X, et al. Catechol determination in compost bioremediation using a laccase sensor and artificial neural networks[ J]. Analytical and Bioanalytical Chemistry, 2008,391 (2) : 679-685.
  • 5Asan A, Isildak I. Determination of major phenolic compounds in water by reversed-phase liquid chromatography after pre-column derivatization with benzoyl chloride [ J ]. Journal of Chromatography A, 2003, 988( 1 ) : 145-149.
  • 6Pistonesi M F, Di Nezio M S, Determination of phenol, resorcinol samples by synchronous fluorescence (PLS) [ J ]. Talanta, 2006, 69 (5) : Centuri6n M E, et al. and hydroquinone in air using partial least-squares 1265-1268.
  • 7Garcia-Mesa J A, Mateos R. Direct automatic determination of bitterness and total phenolic compounds in virgin olive oil using a pH-based flow-injection ana|ysis system [ J ]. Journal of Agricultural and Food Chemistry, 2007, 55(10) : 3863-3868.
  • 8Liu S Q, Yu J H, Ju H X. Renewable phenol biosensor based on a tyrosinase-colloidal gold modified carbon paste electrode [ J]. Journal of Electroanalytical Chemistry, 2003, 540(2): 61-67.
  • 9Mailley P, Cummings E A, Mailley S, et al. Amperometric detection of phenolic compounds by polypyrrole-based composite carbon paste electrodes [ J ]. Bioelectrochemistry, 2004, 63 ( 1- 2) : 291-96.
  • 10Rogers K R, Becker J Y, Cembrano J, et al. Viscosity and binder composition effects on tyrosinase-based carbon paste electrode for detection of phenol and catechol [ J ]. Talanta, 2001, 54(6) : 1059-1065.

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