Article
Determination of Picogram Amounts of Dihydroxybenzenes in Water Samples with Luminol–lysozyme Chemiluminescence System
Article first published online: 15 AUG 2012
DOI: 10.1002/jccs.201200004
Copyright © 2012 The Chemical Society Located in Taipei & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany
Additional Information
How to Cite
Haixiang, Z., Xijuan, T. and Zhenghua, S. (2012), Determination of Picogram Amounts of Dihydroxybenzenes in Water Samples with Luminol–lysozyme Chemiluminescence System. Jnl Chinese Chemical Soc, 59: 1512–1519. doi: 10.1002/jccs.201200004
Publication History
- Issue published online: 29 NOV 2012
- Article first published online: 15 AUG 2012
- Manuscript Accepted: 5 JUN 2012
- Manuscript Received: 3 JAN 2012
- Abstract
- References
- Cited By
Keywords:
- Dihydroxybenzens;
- Lysozyme;
- Water;
- Chemiluminescence;
- Flow injection analysis
Abstract
An ultrasensitive method for the determination of dihydroxybenzens by flow injection (FI) chemiluminescence (CL) analysis was proposed for the first time. It was found that the CL intensity of luminol–lysozyme system could be significantly inhibited by dihydroxybenzens. The CL intensity decrements were linear with the logarithm of dihydroxybenzens concentrations over the ranges of 1.0 ∼ 700 pg mL-1 for hydroquinone (HQ), 5.0 ∼ 700 pg mL-1 for catechol (CT) and 10 ∼ 7000 pg mL-1 for resorcinol (RS), with the corresponding limits of detection of 0.7, 3.0 and 7.0 pg mL-1, respectively. The proposed method was successfully applied to the determination of CT in tap water, rain water, river water and HQ in waste photographic developer samples, with recoveries from 93.5 to 105.8% and relative standard deviations (RSDs) less than 4.0% (n = 5). The possible interaction mechanism of lysozyme with dihydroxybenzens was discussed, and CT to lysozyme's binding constant and the thermodynamic parameters were given by the homemade FI–CL model. The results shown that the binding of dihydroxybenzens to lysozyme was spontaneous with the hydrophobic force.

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