Yantasee Wassana, Charnhattakorn Busarakum, Fryxell Glen E, Lin Yuehe, Timchalk Charles, Addleman R Shane
Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Anal Chim Acta. 2008 Jul 14;620(1-2):55-63. doi: 10.1016/j.aca.2008.05.029. Epub 2008 May 21.
Electrochemical sensors have great potential for environmental monitoring of toxic metal ions in waters due to their portability, field-deployability and excellent detection limits. However, electrochemical sensors employing mercury-free approaches typically suffer from binding competition for metal ions and fouling by organic substances and surfactants in natural waters, making sample pretreatments such as wet ashing necessary. In this work, we have developed mercury-free sensors by coating a composite of thiol self-assembled monolayers on mesoporous supports (SH-SAMMS) and Nafion on glassy-carbon electrodes. With the combined benefit of SH-SAMMS as an outstanding metal preconcentrator and Nafion as an antifouling binder, the sensors could detect 0.5 pp b of Pb and 2.5 pp b of Cd in river water, Hanford groundwater, and seawater with a minimal amount of preconcentration time (few minutes) and without any sample pretreatment. The sensor could also detect 2.5 pp b of Cd, Pb, and Cu simultaneously. The electrodes have long service times and excellent single and inter-electrode reproducibility (5% R.S.D. after 8 consecutive measurements). Unlike SAMMS-carbon paste electrodes, the SAMMS-Nafion electrodes were not fouled in samples containing albumin and successfully detected Cd in human urine. Other potentially confounding factors affecting metal detection at SAMMS-Nafion electrodes were studied, including pH effect, transport resistance of metal ions, and detection interference. With the ability to reliably detect low metal concentration ranges without sample pretreatment and fouling, SAMMS-Nafion composite sensors have the potential to become the next-generation metal analyzers for environmental and bio-monitoring of toxic metals.
电化学传感器因其便携性、现场可部署性和出色的检测限,在水体中有毒金属离子的环境监测方面具有巨大潜力。然而,采用无汞方法的电化学传感器通常会面临金属离子的结合竞争以及天然水体中有机物质和表面活性剂的污染问题,这使得诸如湿式灰化等样品预处理成为必要。在这项工作中,我们通过在玻碳电极上涂覆介孔载体上的硫醇自组装单分子层(SH-SAMMS)和Nafion的复合材料,开发了无汞传感器。借助SH-SAMMS作为出色的金属预浓缩剂和Nafion作为防污粘合剂的综合优势,这些传感器能够在极少的预浓缩时间(几分钟)且无需任何样品预处理的情况下,检测河水、汉福德地下水和海水中0.5 ppb的铅和2.5 ppb的镉。该传感器还能同时检测2.5 ppb的镉、铅和铜。这些电极具有较长的使用寿命以及出色的单电极和电极间重现性(连续8次测量后相对标准偏差为5%)。与SAMMS-碳糊电极不同,SAMMS-Nafion电极在含有白蛋白的样品中不会被污染,并能成功检测人尿中的镉。研究了影响SAMMS-Nafion电极金属检测的其他潜在混杂因素,包括pH效应、金属离子的传输阻力和检测干扰。由于能够在无需样品预处理和不被污染的情况下可靠地检测低金属浓度范围,SAMMS-Nafion复合传感器有潜力成为用于有毒金属环境和生物监测的下一代金属分析仪。