Amaia Soto Beobide

Dr. Amaia Soto Beobide

Institute of Chemical Engineering Sciences, Foundation for Research and Technology-Hellas, 26504 Patras, Greece
orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 August 2017 in Journal of Raman Spectroscopy
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Journal Article
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JAJ.A. Anastasopoulos
J.A. Anastasopoulos
ABAmaia Soto Beobide
Amaia Soto Beobide
AMANASTASIOS MANIKAS
ANASTASIOS MANIKAS
George VoyiatzisGeorge Voyiatzis
George Voyiatzis

15 April 2025 in Biomass Conversion and Biorefinery
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PTPanagiotis Tsaousis
Panagiotis Tsaousis
MSMirva Sarafidou
Mirva Sarafidou
ABAmaia Soto Beobide
Amaia Soto Beobide
GMGeorgios Ν. Mathioudakis
Georgios Ν. Mathioudakis
Katiana FilippiKatiana Filippi
Katiana Filippi
George VoyiatzisGeorge Voyiatzis
George Voyiatzis
A fairly simple yet efficient quantitative protocol was developed to investigate plant composition using Fourier-transform infrared spectroscopy (FTIR), through biomass analysis arising from the whole shoot system of Cardoon (Cynara cardunculus L.), Cannabis (Cannabis sativa L.) and Switchgrass (Panicum virgatum L.). An analytical compositional report of the biomasses, serving as a standard method to identify the different chemical groups present, was compared with relevant FTIR spectra and Thermogravimetric Analysis (TGA) thermographs. In order to interpret the highly convoluted absorption spectra, not only a series of reference materials were examined but also extraction protocols were implemented to sequentially isolate the compositional units allowing a spectroscopic monitoring of their progressive removal from the biomass. This approach enabled the assignment and distinction of a series of vibrational peaks and regions identified in the lower wavenumber region. These peaks/regions, were found to be capable of quantitating different chemical units, such as lignin, fats and lipids, even in the case of structural polysaccharides, like cellulose, hemicellulose and pectin, which are the primary constituents of plant cells. Fats and lipids were easily detected at the 3050–2800 cm−1 region, with their concentration determined by the isolated 720 cm−1 and the 728 cm−1 peaks, when present. Lignin concentration was determined via the 1508 cm−1 peak. Hemicellulose is contributing to the 1640, 1245 cm−1 as well as the 1740 cm−1 peak, with its concentration determined in the 850–750 cm−1 region. Cellulose content was quantified via the 895 cm−1 peak, while pectin appeared at the 915 cm−1 peak and also contributed to the 1640 cm−1 signal. Consequently, a better understanding of the vibrational convolution could thus be achieved when studying plant cells where multiple structural units contribute to the spectra. It is therefore expected that plant cellular composition can be adequately revealed with a single FTIR spectrum, without the need for intensive analysis methods, offering a faster and more efficient approach.

10 June 2015 in Waste and Biomass Valorization
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Georgia AntonopoulouGeorgia Antonopoulou
Georgia Antonopoulou
GDGeorge Dimitrellos
George Dimitrellos
ABAmaia Soto Beobide
Amaia Soto Beobide
Dimitris VayenasDimitris Vayenas
Dimitris Vayenas
GLGerasimos Lyberatos
Gerasimos Lyberatos

1 January 2005 in Journal of Controlled Release
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Journal Article
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SIS.M. Iconomopoulou
S.M. Iconomopoulou
AAAikaterini K Andreopoulou
Aikaterini K Andreopoulou
ABAmaia Soto Beobide
Amaia Soto Beobide
JKJ.K. Kallitsis
J.K. Kallitsis
GVG.A. Voyiatzis
G.A. Voyiatzis

5 February 2002 in Macromolecules
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Journal Article
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ABAmaia Soto Beobide
Amaia Soto Beobide
GVG. A. Voyiatzis
G. A. Voyiatzis

8 November 2020 in Polymers
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Journal Article
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VAVasiliki F. Alexiou
Vasiliki F. Alexiou
GMGeorgios Ν. Mathioudakis
Georgios Ν. Mathioudakis
KAKonstantinos S. Andrikopoulos
Konstantinos S. Andrikopoulos
ABAmaia Soto Beobide
Amaia Soto Beobide
George VoyiatzisGeorge Voyiatzis
George Voyiatzis
Hybrid polymeric materials incorporating carbon nanostructures or inorganic constituents stand as a promising class of materials exhibiting distinct but also complementary features. Carbon nanotubes have been proposed as unique candidates for polymer reinforcement; however, sustained efforts are further needed in order to make full use of their potential. The final properties of the reinforced polymer are controlled in part by the morphology and the eventual molecular orientation of the polymer matrix. In the present study, multiwall carbon nanotubes (MWCNTs) were utilized in order to reinforce polyethylene terephthalate (PET) composites. The effect of CNTs on the crystallization and the orientation of the structurally hybridized polymeric material has been investigated from the perspective of assessing their impact on the final properties of a relevant nanocomposite product. Functionalized MWCNTs were used to achieve their optimal dispersion in the polymer matrix. The physical properties of the composites (i.e., crystallinity and orientation) were characterized via differential scanning calorimetry, X-ray diffraction, and polarized Raman microscopy. The addition of well-dispersed CNTs acted as a nucleation agent, increasing the crystallization of the polyethylene terephthalate matrix and differentiating the orientation of both CNTs and macromolecular chains.