Electrochemical detection of trace silver

电位滴定法 电化学 银纳米粒子 纳米技术 电极 电分析法 伏安法 化学 循环伏安法 剥离(纤维) 材料科学 分析化学(期刊) 纳米颗粒 色谱法 物理化学 生物化学 复合材料
作者
Kequan Xu,Clara Pérez‐Ràfols,María Cuartero,Gastón A. Crespo
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:374: 137929-137929 被引量:21
标识
DOI:10.1016/j.electacta.2021.137929
摘要

Increasing utilization of silver and silver nanoparticles (AgNPs) in daily processes and products has led to a significant growth in scientific interest in methods for monitoring silver. In particular, the amount of silver ions (Ag+) released to the environment is known to have a detrimental effect on aquatic ecology, and thus some control actions have been implemented in recent years; for example, the manufacturing industry is now required to control and certify the quantity of AgNPs present in products. Electrochemical sensors are well suited to the task of silver monitoring due to several beneficial properties, including low costs, fast measurements, and facile adaptation to miniaturized, portable instrumentation. The predominant method for electrochemical silver determination involves potentiometric ion selective electrodes (ISEs) and voltammetric measurements. Reviewing the literature of the last ten years reveals significant improvements in the analytical performance of electrochemical sensors, mainly related to the development of new protocols, selective receptors, and electrode materials. Remarkably, ISEs with limits of detection (LOD) in the nanomolar range have been reported, employing careful control of ion fluxes across the membrane interfaces. What's more, sub-nanomolar LODs are attainable by stripping voltammetry using either ligand-based deposition strategies or thin layer membranes coupled to conducting polymers. Selectivity has also been optimized through the membrane composition of ISEs, with special focus on Ag+ ionophores. Furthermore, novel voltammetric methods allow for discrimination between Ag+ and AgNPs. However, there is still a dearth of studies applying such electrochemical sensors to on-site water analysis, and hence, further research is needed in order to translate these laboratory scale achievements to real-world contexts. Overall, this review describes the state-of-the-art in electrochemical silver detection, and provides a comprehensive description of those aspects contributing to the further development and improvement of analytical performance.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
蔡从安发布了新的文献求助10
1秒前
张张发布了新的文献求助10
1秒前
1秒前
yz发布了新的文献求助10
3秒前
3秒前
4秒前
JamesPei应助YYJ25采纳,获得10
6秒前
打打应助LB采纳,获得10
7秒前
科研通AI6.3应助LB采纳,获得10
7秒前
CipherSage应助LB采纳,获得100
7秒前
8秒前
9秒前
9秒前
雪山飞虎发布了新的文献求助10
10秒前
11秒前
tanx发布了新的文献求助10
12秒前
摘星星吗完成签到 ,获得积分10
13秒前
13秒前
在水一方应助K丶口袋采纳,获得10
14秒前
无极微光应助liyangyang0816采纳,获得20
15秒前
起起发布了新的文献求助10
15秒前
15秒前
小飞鼠爱丽丝完成签到,获得积分10
17秒前
17秒前
隐形曼青应助666sp采纳,获得30
17秒前
dery发布了新的文献求助10
17秒前
小太阳发布了新的文献求助10
19秒前
干净的琦应助Nike采纳,获得30
21秒前
LX应助Nike采纳,获得10
21秒前
侯康应助Nike采纳,获得10
21秒前
干净的琦应助Nike采纳,获得30
21秒前
深情安青应助Nike采纳,获得30
21秒前
免密那发布了新的文献求助10
23秒前
23秒前
23秒前
Hello应助积极夏青采纳,获得10
24秒前
niu发布了新的文献求助10
25秒前
sherif完成签到,获得积分10
26秒前
Hello应助丸子采纳,获得10
27秒前
28秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
AnnualResearch andConsultation Report of Panorama survey and Investment strategy onChinaIndustry 1000
機能性マイクロ細孔・マイクロ流体デバイスを利用した放射性核種の 分離・溶解・凝集挙動に関する研究 1000
卤化钙钛矿人工突触的研究 1000
Engineering for calcareous sediments : proceedings of the International Conference on Calcareous Sediments, Perth 15-18 March 1988 / edited by R.J. Jewell, D.C. Andrews 1000
Continuing Syntax 1000
Harnessing Lymphocyte-Cytokine Networks to Disrupt Current Paradigms in Childhood Nephrotic Syndrome Management: A Systematic Evidence Synthesis 700
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6259273
求助须知:如何正确求助?哪些是违规求助? 8081418
关于积分的说明 16884849
捐赠科研通 5331112
什么是DOI,文献DOI怎么找? 2837912
邀请新用户注册赠送积分活动 1815316
关于科研通互助平台的介绍 1669221