Call: +34 876 553 510
Email: arua@unizar.es
Address: c/Pedro Cerbuna 12, Universidad de Zaragoza, Facultad de Ciencias, Departamento de Química Analítica – Zaragoza (Spain)
ABOUT ME
Ana María Rua Ibarz obtained her Bachelor and Master degrees in Chemistry from the University of Zaragoza (Zaragoza, Spain). She carried out her PhD research at Ghent University (Ghent, Belgium) focused on method development and applications of high-precision isotopic analysis of Hg using cold-vapor generation multi-collector ICP-mass spectrometry instrumentation (CVG-MC-ICP-MS), and he obtained her PhD degree in 2018. In May 2018, after a competitive selection procedure held among international researchers, Ana obtained a postdoctoral position at the Flemish Institute for Technological Research (VITO) in Mol (Belgium), for carrying out a research project intended to explore new analytical strategies for nanoparticle characterization. In March 2020, she started working as postdoctoral researcher at Ghent University on a project in collaboration with TotalEnergies (Feluy, Belgium). The project was based on method development for quantitative elemental and spatially resolved analysis of relevant samples in petrochemistry, such as catalysts, polymers and rocks via laser ablation ICP-MS (LA-ICP-MS). Since November 2022, she is working as postdoctoral researcher at the University of Zaragoza (Spain) after she was awarded a Marie Sklodowska-Curie (MSCA)-COFUND International Fellowship Programme for Talent Attraction to the Campus of International Excellence Campus Iberus. Her research project is entitled “Exploring new venues for the characterization of nanomaterials and microplastics via plasma spectroscopy”.
PUBLICATIONS
2019
Bolea-Fernandez, Eduardo; Leite, Diego; Rua-Ibarz, Ana; Liu, Tong; Woods, Glenn; Aramendia, Maite; Resano, Martín; Vanhaecke, Frank
On the effect of using collision/reaction cell (CRC) technology in single-particle ICP-mass spectrometry (SP-ICP-MS) Journal Article
En: Analytica Chimica Acta, vol. 1077, pp. 95-106, 2019, ISSN: 0003-2670.
@article{BOLEAFERNANDEZ201995,
title = {On the effect of using collision/reaction cell (CRC) technology in single-particle ICP-mass spectrometry (SP-ICP-MS)},
author = {Eduardo Bolea-Fernandez and Diego Leite and Ana Rua-Ibarz and Tong Liu and Glenn Woods and Maite Aramendia and Martín Resano and Frank Vanhaecke},
url = {https://www.sciencedirect.com/science/article/pii/S0003267019306920},
doi = {https://doi.org/10.1016/j.aca.2019.05.077},
issn = {0003-2670},
year = {2019},
date = {2019-01-01},
journal = {Analytica Chimica Acta},
volume = {1077},
pages = {95-106},
abstract = {In this work, the effects of using collision/reaction cell (CRC) technology in quadrupole-based ICP-MS (ICP-QMS) instrumentation operated in single-particle (SP) mode have been assessed. The influence of (i) various CRC gases, (ii) gas flow rates, (iii) nanoparticle (NP) sizes and (iv) NP types was evaluated using Ag, Au and Pt NPs with both a traditional ICP-QMS instrument and a tandem ICP-mass spectrometer. It has been shown that using CRC technology brings about a significant increase in the NP signal peak width (from 0.5 up to 6 ms). This effect is more prominent for a heavier gas (e.g., NH3) than for a lighter one (e.g., H2 or He). At a higher gas flow rate and/or for larger particle sizes >100 nm), the NP signal duration was prolonged to a larger extent. This effect of using CRC technology has been further demonstrated by characterizing custom-made 50 and 200 nm Fe3O4 NPs (originally strongly affected by the occurrence of spectral overlap) using different CRC approaches (H2 on-mass and NH3 mass-shift). The use of NH3 (monitoring of Fe as the Fe(NH3)2+ reaction product ion at m/z = 90 amu) induces a significant peak broadening compared to that observed when using H2 (6.10 ± 1.60 vs. 0.94 ± 0.49 ms). This extension of transit time can most likely be attributed to the collisions/interactions of the ion cloud generated by a single NP event with the CRC gas and it even precludes 50 nm Fe3O4 NPs to be detected when using the NH3 mass-shift approach. Based on these results, the influence of a longer peak width on the accuracy of SP-ICP-MS measurement data (NP size, particle number density and mass concentration) must be taken into account when using CRC technology as a means to overcome spectral overlap. To mitigate the potential detrimental effect of using CRC technology in the characterization of NPs via SP-ICP-MS(/MS), the use of light gases and low gas flow rates is recommended.},
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2017
Bolea-Fernandez, Eduardo; Leite, Diego; Rua-Ibarz, Ana; Balcaen, Lieve; Aramendía, Maite; Resano, Martín; Vanhaecke, Frank
Characterization of SiO2 nanoparticles by single particle-inductively coupled plasma-tandem mass spectrometry (SP-ICP-MS/MS) Journal Article
En: J. Anal. At. Spectrom., vol. 32, iss. 11, pp. 2140-2152, 2017.
@article{C7JA00138J,
title = {Characterization of SiO2 nanoparticles by single particle-inductively coupled plasma-tandem mass spectrometry (SP-ICP-MS/MS)},
author = {Eduardo Bolea-Fernandez and Diego Leite and Ana Rua-Ibarz and Lieve Balcaen and Maite Aramendía and Martín Resano and Frank Vanhaecke},
url = {http://dx.doi.org/10.1039/C7JA00138J},
doi = {10.1039/C7JA00138J},
year = {2017},
date = {2017-01-01},
journal = {J. Anal. At. Spectrom.},
volume = {32},
issue = {11},
pages = {2140-2152},
publisher = {The Royal Society of Chemistry},
abstract = {The increase in the use of SiO2 nanoparticles (NPs) is raising concern about their environmental and health effects, thus necessitating the development of novel methods for their straightforward detection and characterization. Single particle ICP-mass spectrometry (SP-ICP-MS) is able to provide information on the size of NPs, their particle number density and mass concentration. However, the determination of Si via ICP-MS is strongly hampered by the occurrence of spectral overlap from polyatomic species (e.g., CO+ and N2+). The use of tandem ICP-MS (ICP-MS/MS) enables interference-free conditions to be obtained, even in the most demanding applications. Upon testing several gases, the use of CH3F (monitoring of SiF+, mass-shift approach) and of H2 (monitoring of Si+, on-mass approach) were demonstrated to be the most suitable to overcome the spectral interference affecting ultra-trace Si determination (LoD < 15 ng L−1). By using these approaches, SiO2 NPs (ranging between 80 and 400 nm) can be detected and characterized. For SiO2 NPs > 100 nm, it was possible to provide accurate results in a straightforward way, as the signals they give rise to are well resolved from those of the background. In the case of 80 and 100 nm NPs, the use of a simple deconvolution approach following a Gaussian model was needed to characterize SiO2 NPs apparently showing incomplete distributions as a result of the presence of the background signal. Overall, the methods developed using SP-ICP-MS/MS are sensitive and selective enough for the interference-free determination of Si at ultra-trace levels, also in the form of SiO2 NPs.},
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pubstate = {published},
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}
0000
Bazo, Antonio; Bolea-Fernandez, Eduardo; Rua-Ibarz, Ana; Aramendía, Maite; Resano, Martín
En: Analytical Chemistry, vol. 0, no. 0, pp. null, 0000, (PMID: 40481769).
@article{doi:10.1021/acs.analchem.5c01588,
title = {Ions with Ions, Entities with Entities: A Proof-of-Concept Study Using the SELM-1 Yeast Certified Reference Material for Intra- and Extracellular Se Quantification via Single-Cell ICP-Mass Spectrometry},
author = {Antonio Bazo and Eduardo Bolea-Fernandez and Ana Rua-Ibarz and Maite Aramendía and Martín Resano},
url = {https://doi.org/10.1021/acs.analchem.5c01588},
doi = {10.1021/acs.analchem.5c01588},
journal = {Analytical Chemistry},
volume = {0},
number = {0},
pages = {null},
note = {PMID: 40481769},
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Bazo, Antonio; Bolea-Fernandez, Eduardo; Rua-Ibarz, Ana; Aramendía, Maite; Resano, Martín
En: Analytical Chemistry, vol. 0, no. 0, pp. null, 0000, (PMID: 40481769).
@article{doi:10.1021/acs.analchem.5c01588b,
title = {Ions with Ions, Entities with Entities: A Proof-of-Concept Study Using the SELM-1 Yeast Certified Reference Material for Intra- and Extracellular Se Quantification via Single-Cell ICP-Mass Spectrometry},
author = {Antonio Bazo and Eduardo Bolea-Fernandez and Ana Rua-Ibarz and Maite Aramendía and Martín Resano},
url = {https://doi.org/10.1021/acs.analchem.5c01588},
doi = {10.1021/acs.analchem.5c01588},
journal = {Analytical Chemistry},
volume = {0},
number = {0},
pages = {null},
note = {PMID: 40481769},
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Rua-Ibarz, Ana; Nakadi, Flávio V.; Bolea-Fernandez, Eduardo; Bazo, Antonio; Battistella, Beatrice; Matiushkina, Anna; Resch-Genger, Ute; Abad, Carlos; Resano, Martín
Discrete Entity Analysis via Microwave-Induced Nitrogen Plasma–Mass Spectrometry in Single-Event Mode Journal Article
En: Analytical Chemistry, vol. 0, no. 0, pp. null, 0000, (PMID: 41084806).
@article{doi:10.1021/acs.analchem.5c04341,
title = {Discrete Entity Analysis via Microwave-Induced Nitrogen Plasma–Mass Spectrometry in Single-Event Mode},
author = {Ana Rua-Ibarz and Flávio V. Nakadi and Eduardo Bolea-Fernandez and Antonio Bazo and Beatrice Battistella and Anna Matiushkina and Ute Resch-Genger and Carlos Abad and Martín Resano},
url = {https://doi.org/10.1021/acs.analchem.5c04341},
doi = {10.1021/acs.analchem.5c04341},
journal = {Analytical Chemistry},
volume = {0},
number = {0},
pages = {null},
note = {PMID: 41084806},
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pubstate = {published},
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}