4.6 Article

Dithiocarbamate-capped silver nanoparticles as a resonance light scattering probe for simultaneous detection of lead(II) ions and cysteine

期刊

ANALYST
卷 138, 期 8, 页码 2420-2426

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3an36868h

关键词

-

资金

  1. Natural Science Foundation of China [21277111]
  2. Fundamental Research Funds for the Central Universities [XDJK2013D001]
  3. State Key Laboratory Breeding Base of Eco-Environments and Bio-Resources of the Three Gorges Reservoir Region [SKL-2011-08]

向作者/读者索取更多资源

We investigated the suitability of dithiocarbamate (DTC) capped Ag nanoparticles (NPs) as resonance light scattering (RLS) probes for the simultaneous sensing of Pb2+ and cysteine. The DTC capping ligands are generated by a very simple in situ method through reaction of carbon disulfide with diethanolamine as primary precursor molecules under ultrasonic irradiation. This strategy was based on the fact that Pb2+ could induce the aggregation of DTC-Ag NPs due to the strong metal affinity of DTC along with an enhanced RLS signal. After optimizing some experimental conditions (including the pH value of the solution, concentration of DTC-Ag NPs, and ion strength), a very simple and facile sensing system has been developed for the detection of Pb2+ in water based on RLS technology. The proposed system promises excellent selectivity, a wide linear response range and high sensitivity for Pb2+. The linear response range for Pb2+ was from 0.01 mu M to 60 mu M. The limit of detection (S/N = 3 sigma) for Pb2+ was as low as 4 nM. The proposed method was successfully used to detect Pb2+ in river and tap water samples, indicating the potential of this new, sensitive and selective method in water quality monitoring. Meanwhile, due to the strong binding preference of cysteine toward Pb2+ by the formation of Pb2+-S bonds, Pb2+ was removed from the surfaces of the DTC-Ag NPs, leading to redispersion of DTC-Ag NPs, along with a decreased RLS signal. The possibility of the proposed system for the sensing of cysteine was also investigated.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据