Yolanda Patiño

Dr. Yolanda Patiño

University of Oviedo, Oviedo, Asturias, Spain
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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1 October 2015 in Chemosphere
Verified
Journal Article
Closed access
YPYolanda Patiño
Yolanda Patiño
Eva DiazEva Diaz
Eva Diaz
Salvador OrdoñezSalvador Ordoñez
Salvador Ordoñez
EGEsteban Gallegos-Suarez
Esteban Gallegos-Suarez
Antonio Guerrero RuizAntonio Guerrero Ruiz
Antonio Guerrero Ruiz
Inmaculada Rodríguez-RamosInmaculada Rodríguez-Ramos
Inmaculada Rodríguez-Ramos

1 December 2012 in International Journal of Hydrogen Energy
Verified
Journal Article
Closed access
PMPablo Marín
Pablo Marín
YPYolanda Patiño
Yolanda Patiño
FDFernando V. Díez
Fernando V. Díez
Salvador OrdoñezSalvador Ordoñez
Salvador Ordoñez

1 January 2015 in Chemosphere
Verified
Journal Article
Closed access
YPYolanda Patiño
Yolanda Patiño
Eva DiazEva Diaz
Eva Diaz
Salvador OrdoñezSalvador Ordoñez
Salvador Ordoñez

1 January 2018 in Bioresource Technology
Verified
Journal Article
Open access
YPYolanda Patiño
Yolanda Patiño
LMLaura G. Mantecón
Laura G. Mantecón
SPSara Polo
Sara Polo
LFLaura Faba
Laura Faba
Eva DiazEva Diaz
Eva Diaz
Salvador OrdoñezSalvador Ordoñez
Salvador Ordoñez
Secondary sludge from municipal wastewater treatment plant is proposed as a promising alternative lipid feedstock for biodiesel production. A deep study combining different type of raw materials (sludge coming from the oxic, anoxic and anaerobic steps of the biological treatment) with different technologies (liquid-liquid and solid-liquid extractions followed by acid catalysed transesterification and in situ extraction-transesterification procedure) allows a complete comparison of available technologies. Different parameters - contact time, catalyst concentration, pretreatments - were considered, obtaining more than 17% FAMEs yield after 50min of sonication with the in situ procedure and 5% of H2SO4. This result corresponds to an increment of more than 65% respect to the best results reported at typical conditions. Experimental data were used to propose a mathematical model for this process, demonstrating that the mass transfer of lipids from the sludge to the liquid is the limiting step.

1 January 2016 in Chemical Engineering Journal
Verified
Journal Article
Closed access
YPYolanda Patiño
Yolanda Patiño
Eva DiazEva Diaz
Eva Diaz
Salvador OrdoñezSalvador Ordoñez
Salvador Ordoñez

1 February 2019 in Water Science & Technology
Verified
Journal Article
Closed access
PDF file
Eva DiazEva Diaz
Eva Diaz
SSSonia Stożek
Sonia Stożek
YPYolanda Patiño
Yolanda Patiño
Salvador OrdoñezSalvador Ordoñez
Salvador Ordoñez
Naproxen (NPX) degradation was investigated by anodic oxidation both at constant potential and by cyclic voltammetry, using this last technique for optimizing reaction conditions and catalyst properties. Three MWCNTs-promoted electrodes were used (MWCNT, MWCNT-COOH and MWCNT-NH2) and a two steps oxidation process being observed in all the cases. At the optimized conditions (volume of MWCNT = 15 μL), the influence of the scan rate indicates the diffusion – adsorption control of the process. Likewise, the kinetic study of NPX degradation at fix potential, considering two different stirring speeds (250 and 500 rpm), indicates that degradation rate increases with the stirring speed. After 20 h, NPX is degraded even an 82.5%, whereas the mineralization reaches almost 70% as it was obtained from total organic carbon analysis. PH effect was also analysed, in the range 5–11, observing a positive effect at low pH. Concerning the surface chemistry of the electrode, MWCNT-NH2, with the highest isoelectric point (4.70), is the most promising material due to the improved interactions with the reactant. From these observations, a pathway is proposed, which includes two steps of electrochemical oxidation followed by subsequent oxidation steps, until mineralization of the NPX, attributed mainly to active chlorine species and ·OH.