2015
DOI: 10.1039/c4ay02199a
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Sensitive determination of catechol using a glassy carbon electrode modified with l-cysteine and ZnS:Ni/ZnS quantum dots

Abstract: In this work, water-soluble ZnS:Ni/ZnS quantum dots (QDs) with core/shell structure were obtained successfully using mercaptoacetic acid as dressing agent, which were characterized by X-ray diffraction, fourier transform infrared spectroscopy, atomic force microscopy and transmission electron microscope. A highly sensitive and stable electrochemical sensor was developed through immobilizing L-Cysteine and ZnS:Ni/ZnS QDs on the surface of glassy carbon electrode. The sensor showed excellent catalytic activity t… Show more

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Cited by 10 publications
(2 citation statements)
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“… Haruta et al (2001) propose that PPO contributes to aspen defense by enhancing the toxicity of catechol, and that release of catechol and PPO oxidation is a possible mechanism of toxicity in trembling aspen ( Populus tremuloides ). Indeed, approximately 50% of synthetic catechol is used to consume for pesticides ( Qu et al, 2015 ). Therefore, catechol in transgenic lines has likely a role in insect resistance.…”
Section: Discussionmentioning
confidence: 99%
“… Haruta et al (2001) propose that PPO contributes to aspen defense by enhancing the toxicity of catechol, and that release of catechol and PPO oxidation is a possible mechanism of toxicity in trembling aspen ( Populus tremuloides ). Indeed, approximately 50% of synthetic catechol is used to consume for pesticides ( Qu et al, 2015 ). Therefore, catechol in transgenic lines has likely a role in insect resistance.…”
Section: Discussionmentioning
confidence: 99%
“…Dihydroxybenzene isomers, hydroquinone (HQ), catechol (CC) and resorcinol (RC), are derived from a wealth of sources, including agriculture, factory discharges, wastewater treatment plants and other related industries. [1][2][3] Owing to their low degradation in the environment and high toxicity to the environment and humans, the US Environmental Protection Agency (EPA) and the European Union have classied dihydroxybenzene isomers as environmental pollutants. 4 Therefore, simultaneous determination of dihydroxybenzene isomers has become a hot topic for scientists.…”
Section: Introductionmentioning
confidence: 99%