Evaporation dynamics of sessile droplets in the ablation cell for LA-ICP-MS analysis of liquids

IF 5.7 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Petr Rudolf , Kristýna Lapčíková , Alena Randová , Antonín Kaňa
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引用次数: 0

Abstract

Background

Inductively coupled plasma mass spectrometry (ICP-MS) is a powerful method for elemental analysis. However, it faces challenges when analysing organic-rich samples due to plasma instability. Laser ablation coupled with ICP-MS (LA-ICP-MS) offers a suitable alternative by introducing minimal sample amounts into the plasma, maintaining its stability. In the case of liquids, rapid evaporation of liquid droplets limits the applicability of LA-ICP-MS, as it impacts analyte concentration. Understanding droplet evaporation dynamics within the ablation cell, where helium accelerates droplet evaporation, is essential to improve reliability of the analysis. This study explores the evaporation behaviour of organic solvent droplets in LA-ICP-MS. In addition, it aims to enhance liquid sample analysis by modelling observed evaporation processes.

Results

Experiments were conducted with organic solvent droplets evaporating on various sample-holder surfaces, focusing on evaporation within helium and air environments. Polytetrafluoroethylene (PTFE) was identified as the optimal surface material for sustaining high contact angles of sessile droplets, thus prolonging droplet lifetime. A mathematical model was developed to describe evaporation, incorporating contact angle, droplet geometry, and mass transfer dynamics. The model demonstrates that most droplets initially evaporate in a constant contact radius mode, then transition to a constant contact angle mode. The experimental data align closely with the model predictions, affirming the impact of initial contact angle and droplet volume on evaporation behaviour. Additionally, we established correlations to predict droplet lifetime based on saturated vapour pressure and initial droplet height, contributing a practical reference for management of organic solvents in LA-ICP-MS applications.

Significance and novelty

This research provides a straightforward approach to understanding and controlling evaporation dynamics of liquid samples in LA-ICP-MS, which is essential for reliable elemental analysis of organic-rich liquid samples. By modelling sessile droplet behaviour and validating it with experimental data, this study lays the groundwork for a wide range of applications, such as the analysis of metals in oils and other low-volatility organic solvents or analysis of microliter-scale liquid samples.

Abstract Image

Abstract Image

液体LA-ICP-MS分析烧蚀池中液滴的蒸发动力学
电感耦合等离子体质谱(ICP-MS)是一种强大的元素分析方法。然而,由于等离子体的不稳定性,它在分析富含有机物的样品时面临挑战。激光烧蚀结合ICP-MS (LA-ICP-MS)提供了一种合适的替代方案,通过将最小的样品量引入等离子体,保持其稳定性。在液体的情况下,液滴的快速蒸发限制了LA-ICP-MS的适用性,因为它会影响分析物的浓度。在氦加速液滴蒸发的烧蚀池中,了解液滴蒸发动力学对于提高分析的可靠性至关重要。本研究探讨了有机溶剂液滴在LA-ICP-MS中的蒸发行为。此外,它旨在通过模拟观察到的蒸发过程来增强液体样品分析。结果对有机溶剂液滴在不同样品架表面的蒸发进行了实验,重点研究了在氦气和空气环境下的蒸发。聚四氟乙烯(PTFE)是维持液滴高接触角、延长液滴寿命的最佳表面材料。建立了一个数学模型来描述蒸发,包括接触角、液滴几何形状和传质动力学。该模型表明,大多数液滴最初以恒定接触半径模式蒸发,然后转变为恒定接触角模式。实验数据与模型预测一致,证实了初始接触角和液滴体积对蒸发行为的影响。此外,我们建立了基于饱和蒸气压和初始液滴高度的相关性来预测液滴寿命,为LA-ICP-MS应用中有机溶剂的管理提供了实用参考。意义与创新本研究为了解和控制LA-ICP-MS中液体样品的蒸发动力学提供了一种简单的方法,这对富有机物液体样品的可靠元素分析至关重要。通过模拟液滴的行为并用实验数据验证,本研究为广泛的应用奠定了基础,例如分析油和其他低挥发性有机溶剂中的金属或分析微升规模的液体样品。
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来源期刊
Analytica Chimica Acta
Analytica Chimica Acta 化学-分析化学
CiteScore
10.40
自引率
6.50%
发文量
1081
审稿时长
38 days
期刊介绍: Analytica Chimica Acta has an open access mirror journal Analytica Chimica Acta: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. Analytica Chimica Acta provides a forum for the rapid publication of original research, and critical, comprehensive reviews dealing with all aspects of fundamental and applied modern analytical chemistry. The journal welcomes the submission of research papers which report studies concerning the development of new and significant analytical methodologies. In determining the suitability of submitted articles for publication, particular scrutiny will be placed on the degree of novelty and impact of the research and the extent to which it adds to the existing body of knowledge in analytical chemistry.
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