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Fluorine (F) plays an important role in biology and geology but is hard to analyse and quantify using element-specific techniques. This is related to its high first ionisation potential and analytical methods depending on high energy sources for excitation and/or ionisation of F. In particular ICP-MS was initially found incapable of detecting F; however, recent methodological advances, i.e., the application of Ba as a plasma modifier and the application of tandem mass spectrometry, enabled its analysis by targeting BaF+. In this study, we suggest this approach in conjunction with laser ablation to perform the mapping of F in both biological and geological samples. In a proof of concept, tooth samples as biological samples and a Rhynie chert as a geological sample were analysed. For method development and to evaluate the performance of the developed method, gelatine-based F-standards were prepared and characterised using combustion ion chromatography. Standards were further interrogated to estimate LODs and LOQs. Depending on the required spatial resolution, figures of merit in the upper ng g−1 range and lower μg g−1 range were achievable. This is the first example of F mapping using LA-ICP-MS instrumentation and the developed methods close an important analytical gap by enabling the spatially resolved F analysis at relevant biological and geological concentrations. [ABSTRACT FROM AUTHOR]

Elemental analysis of fluorochemicals has received renewed attention in recent years stemming from the increased use of fluorinated compounds. However, fundamental drawbacks of in-plasma ionization have hindered ICPMS applications in this area. Recently, we have introduced post-ICP chemical ionization for BaF+ formation using Ba-containing reagent ions supplied by nanospray, leading to major improvements in F detection sensitivity. Here, we present further insights into this post-plasma chemical ionization. First, we examine the effect of oxygen introduced into the plasma (a necessity for organic solvent introduction) on BaF+ ion formation. The results indicate that excess plasma oxygen leads to abundant HNO3 in the post-plasma flow, shifting ionization reactions toward BaNO3+ formation and suppressing BaF+ sensitivity. To amend this, we utilize reagent ions with other metal centers to impart selectivity toward F detection. Our investigations show that robustness of F detection in the presence of abundant HNO3 improves in the order Al3+ ≈ Sc3+ > La3+ > Mg2+ > Ba2+ as the metal center in the reagent ions, consistent with the stronger metal–F bond in the series. Sc-based ionization resulting in ScNO3F+ shows the best balance between sensitivity and robustness in the presence of nitric acid. Similarly, this ion shows an improved tolerance relative to BaF+ for a Cl-containing matrix where HCl interferes with ionization. Finally, we demonstrate a unique feature of post-plasma chemical ionization for real-time flagging of matrix effects via monitoring reagent ions. These findings provide significant improvements of post-plasma chemical ionization for elemental F analysis, particularly for online chromatographic detection where solvent gradients are utilized. [ABSTRACT FROM AUTHOR]

Increased applications of fluorochemicals have prompted development of elemental methods for detection and quantitation of these compounds. However, high-sensitivity detection of fluorine is a challenge because of difficulties in excitation and ionization of this element. Recently, a new approach has emerged to detect F as a diatomic ion (BaF+) in inductively coupled plasma mass spectrometry (ICP-MS). However, formation of this species in the high-temperature plasma is inefficient, leading to low sensitivities. Here, we introduce a post-ICP chemical ionization approach to enhance analytical performance for F detection in liquid samples. Solutions of fluorochemicals are introduced into an ICP leading to formation of HF in the afterglow. Subsequently, reagent ions from nanospray of sodium acetate and barium acetate electrolytes are utilized to ionize HF to Na2F+ and BaF+, respectively, via post-plasma ion-neutral reactions. Both ions provide substantially better sensitivities compared to that of BaF+ formed inside the plasma in conventional ICP-MS methods. Notably, post-plasma BaF+ offers a sensitivity of 280 cps ppb−1 for F, near two orders of magnitude higher than that of conventional ICP-MS methods. Compound-independent response for F from structurally diverse organofluorines is confirmed by monitoring BaF+ and a limit of detection (LOD) of 8–11 ng mL−1 F is achieved. Importantly, isobaric interferences are substantially reduced in chemical ionization, leaving F background as the main factor in LOD determination. Insights into BaF+ formation via experimental and computational investigations suggest that BaNO2+ and Ba(H2O)n2+ serve as reagent ions while nonreactive BaCH3CO2+ is the dominant ion produced by nanospray. The facile development of effective post-plasma ionization chemistries using the presented approach offers a path for further improvements in F elemental analysis. [ABSTRACT FROM AUTHOR]

A simple and general dried droplet calibration approach was developed for the quantitative analysis of elements in inorganic nonmetallic materials using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). For quantitative analysis, the elemental distribution in dried droplets was improved by optimizing the amount of a surfactant (Pluronic F-127) added into the calibration solutions and the drying temperature. Under optimal conditions, at 2.0 wt% Pluronic F-127 in the calibration solutions and a drying temperature of 85 °C, the relative standard deviation of the signal intensity obtained from multi-line ablation mode is less than 20% for dried droplets. Meanwhile, the experimental results revealed that dried droplets have no effect on the ablation of the sample and dried droplets can be totally ablated in one ablation raster. Further, the method was applied to analyze several inorganic non-metallic materials such as yttrium aluminum garnet (YAG) ceramic, BaF2 crystal, and NIST SRM 612 glass. The linear correlation coefficients of the calibration curves ranged from 0.9936 to 0.9999 without any internal standard correction. Moreover, the results agree well with the results obtained by inductively coupled plasma atomic emission spectrometry or inductively coupled plasma atomic mass spectrometry and certified values. [ABSTRACT FROM AUTHOR]