Comparison of Mg/Ca concentration series from Patella depressa limpet shells using CF-LIBS and LA-ICP-MS.

The elemental composition of marine mollusk shells can offer valuable information about environmental conditions experienced by a mollusk during its lifespan. Previous studies have shown significant correlations between Mg/Ca concentration ratios measured on biogenic carbonate of mollusk shells and sea surface temperature (SST). Here we propose the use of Laser-Induced Breakdown Spectroscopy (LIBS) and the validation of the Calibration-Free LIBS (CF-LIBS) approach for the rapid measurement and estimation of Mg/Ca molar concentration profiles within Patella depressa Pennant, 1777 limpet shells.

Chemometrics and elemental mapping by portable LIBS to identify the impact of volcanogenic and non-volcanogenic degradation sources on the mural paintings of Pompeii.

Crystallization of soluble salts is a common degradation phenomenon that threatens the mural paintings of Pompeii. There are many elements that contribute to the crystallization of salts on the walls of this archaeological site. Notably, the leachates of the pyroclastic materials ejected in 79 AD by Mount Vesuvius and local groundwater, rich in ions from the erosion of volcanic rocks.

Elucidation of the Chemical Role of the Pyroclastic Materials on the State of Conservation of Mural Paintings from Pompeii.

Pyroclastic strata have always been thought to protect the archaeological remains of the Vesuvian area (Italy), hence allowing their conservation throughout the centuries. In this work, we demonstrate that they constitute a potential threat for the conservation state of the mural paintings of Pompeii. The ions that could be leached from them and the ion-rich groundwater coming from the volcanic soil/rocks may contribute to salt crystallisation.

Otoliths as indicators for fish behaviour and procurement strategies of hunter-gatherers in North Patagonia.

This study evaluates the potential use of archaeological otoliths of (Cuvier and Valenciennes) as a tool to study fish behavior and hunter-gatherers procurement strategies on the North Patagonian coast. The studied samples come from the San Antonio archaeological locality dated at ca. 1000-800 C yr BP (Late Holocene).

Volatile organic compound analysis by pulsed glow discharge time of flight mass spectrometry as a structural elucidation tool.

Pulsed glow discharge (PGD) coupled to time of flight mass spectrometry (TOFMS) has been investigated for volatile organic compound (VOC) identification and determination. Optimization of PGD operational conditions (chamber design, applied power, pressure and duty cycle) was performed using acetone and benzene as model compounds. During the different optimizations, molecular, fragment and elemental information were obtained when characteristic GD pulse regions were measured.

An exploratory study of the potential of LIBS for visualizing gunshot residue patterns.

The study of gunshot residue (GSR) patterns can assist in the reconstruction of shooting incidences. Currently, there is a real need of methods capable of furnishing simultaneous elemental analysis with higher specificity for the GSR pattern visualization. Laser-Induced Breakdown Spectroscopy (LIBS) provides a multi-elemental analysis of the sample, requiring very small amounts of material and no sample preparation.

A flowing atmospheric pressure afterglow as an ion source coupled to a differential mobility analyzer for volatile organic compound detection.

Atmospheric pressure glow discharges have been widely used in the last decade as ion sources in ambient mass spectrometry analyses. Here, an in-house flowing atmospheric pressure afterglow (FAPA) has been developed as an alternative ion source for differential mobility analysis (DMA). The discharge source parameters (inter-electrode distance, current and helium flow rate) determining the atmospheric plasma characteristics have been optimized in terms of DMA spectral simplicity with the highest achievable sensitivity while keeping an adequate plasma stability and so the FAPA working conditions finally selected were: 35 mA, 1 L min(-1) of He and an inter-electrode distance of 8 mm.

Analytical potential of a laser ablation-glow discharge-optical emission spectrometry system for the analysis of conducting and insulating materials.

The analytical capabilities of a glow discharge (GD) as a secondary source for excitation/ionization of the material provided by laser ablation (LA) have been compared to conventional laser induced breakdown spectroscopy (LIBS). In LA-GD both sources can be independently adjusted to optimize the sampling process and then its subsequent excitation. This could involve a number of analytical performance advantages, such as reduced matrix dependence, greater precision and sensitivity than those encountered in LIBS.

Characterization of a new mobility separation tool: HRIMS as differential mobility analyzer.

High resolution ion mobility spectrometer (HRIMS) is a new instrument that uses parallel plate Differential Mobility Analysis as principle of separation. Gas phase analysis of volatile organic compounds (VOCs) has been performed for the characterization of this new mobility system using an UV-lamp for ionization. Studies of the effect of temperature and the presence of a desiccant are detailed.

Use of radiofrequency power to enable glow discharge optical emission spectroscopy ultrafast elemental mapping of combinatorial libraries with nonconductive components: nitrogen-based materials.

Combinatorial chemistry and high-throughput techniques are an efficient way of exploring optimal values of elemental composition. Optimal composition can result in high performance in a sequence of material synthesis and characterization. Materials combinatorial libraries are typically encountered in the form of a thin film composition gradient which is produced by simultaneous material deposition on a substrate from two or more sources that are spatially separated and chemically different.

Critical evaluation of the potential of radiofrequency pulsed glow discharge-time-of-flight mass spectrometry for depth-profile analysis of innovative materials.

The combination of radiofrequency pulsed glow discharge (RF-PGD) analytical plasmas with time-of-flight mass spectrometry (TOFMS) has promoted the applicability of this ion source to direct analysis of innovative materials. In this sense, this emerging technique enables multi-elemental depth profiling with high depth resolution and sensitivity, and simultaneous production of elemental, structural, and molecular information. The analytical potential and trends of this technique are critically presented, including comparison with other complementary and well-established techniques (e.

RF-pulsed glow discharge time-of-flight mass spectrometry for glass analysis: investigation of the ion source design.

Radiofrequency (RF) millisecond pulsed glow discharge (PGD) coupled to time-of-flight mass spectrometry (TOFMS) was investigated for direct elemental analysis of glass samples. Aiming at achieving highest elemental sensitivity, appropriate discrimination from polyatomics, and good crater shapes on glasses, a new Grimm-type GD chamber (termed from now "UNIOVI GD", designed and constructed in our laboratory) was coupled to TOFMS, and the results compared with those obtained with the former GD design (here denominated as "GD.1") of the initial RF-PGD-TOFMS prototype.

Thickness determination of subnanometer layers using laser ablation inductively coupled plasma mass spectrometry.

Laser ablation inductively coupled plasma mass spectrometry has been applied to determine the thickness of subnanometer (subnm) metallic layers. Metallic Nd was deposited onto Si wafers with 0.5, 1, 3, and 6 nm thickness and covered by a 10 nm Al coating.

Evaluation of pulsed radiofrequency glow discharge time-of-flight mass spectrometry for precious metal determination in lead fire assay buttons.

In this paper, an exploration of the capabilities and limitations of pulsed radiofrequency glow discharge time-of-flight mass spectrometry (GD-TOFMS) for the determination of the precious metals Ag, Au, Pd, Pt and Rh in lead buttons obtained by Pb fire assay is reported on. Since the matrix consists almost entirely of lead (>99%), the occurrence of doubly charged Pb (Pb(2+)) ions can hinder accurate determination of Rh. This problem was counteracted by relying on the time-resolved formation of different ion types over the pulse period of the glow discharge, which allows discrimination against the Pb(2+) ions.

Pulsed radiofrequency glow discharge time-of-flight mass spectrometry for nanostructured materials characterization.

Progress in the development of advanced materials strongly depends on continued efforts to miniaturizing their structures; thus, a great variety of nanostructured materials are being developed nowadays. Metallic nanowires are among the most attractive nanometer-sized materials because of their unique properties that may lead to applications as interconnectors in nanoelectronic, magnetic, chemical or biological sensors, and biotechnological labels among others. A simple method to develop self-ordered arrays of metallic nanowires is based on the use of nanoporous anodic alumina (NAA) and self-assembled nanotubular titanium dioxide membranes as templates.

Pulsed radiofrequency glow discharge time-of-flight mass spectrometry for molecular depth profiling of polymer-based films.

We demonstrate the potential of an innovative technique, pulsed radiofrequency glow discharge time-of-flight mass spectrometry, for the molecular depth profiling of polymer materials. The technique benefits from the presence, in the afterglow of the pulsed glow discharge, of fragment ions that can be related to the structures of the polymers under study. Thin films of different polymers (PMMA, PET, PAMS, PS) were successfully profiled with retention of molecular information along the profile.

Nitrogen effects in multi-matrix calibrations by radiofrequency glow discharge--optical emission spectrometry.

A study about the effect of nitrogen in the calibration curves of a series of analytical emission lines has been carried out in this work. Fifteen reference materials with different matrices (Fe, Al, Zn, Cu and Ni) were used (three of these reference materials contain nitrogen in their composition) and plots of intensity versus the product "sputtering rate times element concentration" were constructed for emission lines of the analytes considered in this work (Al, Fe, Cu, Cr, C, Mo, Zn, Si, Ti and Ni). Two different fits were performed in each plot, first considering only the points corresponding to samples without nitrogen in their composition and secondly including all the points.

Quantification of bromine in flame-retardant coatings by radiofrequency glow discharge-optical emission spectrometry.

There is an increasing concern regarding the toxicity and environmental distribution and impact of brominated organic compounds employed as flame retardants. Thus, present interest in searching for new analytical techniques and methods allowing a rapid, simple and reliable detection of those compounds in materials and wastes potentially containing such flame retardants is not surprising. The feasibility of using radiofrequency glow discharge plasma spectrometry coupled with optical emission spectrometry (rf-GD-OES) as a rapid and simple tool to directly analyse bromine-containing flame-retardant polymeric layers is investigated here.

In-depth profile analysis of thin films deposited on non-conducting glasses by radiofrequency glow-discharge-optical emission spectrometry.

The potential of radiofrequency glow-discharge-optical emission spectrometry (rf-GD-OES) for quantification of thin films on non-conducting materials has been investigated. A commercial rf-GD chamber from Jobin Yvon operated at 13.56 MHz with Ar as discharge gas was used.

Depth profiling with modified dc-Grimm and rf-Grimm-type glow discharges operated with high gas flow rates and coupled to a high-resolution mass spectrometer.

The improved analytical capability of direct-current (dc) and radiofrequency (rf) "fast flow" glow discharges coupled to a sector field mass spectrometer (GD-SFMS) are presented. In particular, the effect of GD chamber design has been studied to obtain suitable crater shapes for depth-profile analysis of solid samples while maintaining the high sensitivity and stability of this source. In this study it was observed that the distance between the sample surface and the end of the flow tube is critical and so careful optimisation is needed.

A radiofrequency glow-discharge-time-of-flight mass spectrometer for direct analysis of glasses.

A radiofrequency (rf) glow-discharge (GD) ion source coupled to a commercial on-axis time-of-flight mass spectrometer (TOFMS) has been developed for the direct analysis of non-conducting samples. Different instrumental configurations of the rf-GD source, including the optional use of a sampler cone and the possibility of allowing electrical floating of the discharge, were evaluated first with a conducting sample. Higher ion signals were obtained when the GD was electrically floating and no sampler cone was used.

Radiofrequency glow-discharge devices for direct solid analysis.

The enormous potential of radiofrequency glow discharges (rf-GD) as photon, atom, or ion sources, coupled to spectrometric techniques, for rapid direct analysis of almost any conductor, semiconductor, or insulating material with good in-depth resolution has been demonstrated world-wide. This outstanding performance has prompted a great effort to develop and characterise rf-GD for direct materials analysis in recent years. The state of the art of rf-GD coupled to atomic absorption spectrometry, optical emission spectrometry, and mass spectrometry for direct solid analysis is reviewed here.

Radio frequency glow discharge-optical emission spectrometry for direct quantitative analysis of glass.

Direct solid quantitative analysis of glass by radio frequency (rf) glow discharge-optical emission spectrometry (GD-OES) by using special silicate glasses of very different composition (e.g., the SiO(2) content varied from 10 to 70%, the CaO content from 0 to 25%, the Na(2)O content from 0 to 15%, the K(2)O content from 0 to 19%, etc.