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                <text>&lt;p&gt;&lt;strong&gt;Caracterizaci&amp;oacute;n arqueom&amp;eacute;trica de cuentas y cer&amp;aacute;micas prehisp&amp;aacute;nicas de Huanchaco mediante t&amp;eacute;cnicas y m&amp;eacute;todos f&amp;iacute;sicos &lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;Archeometric characterization of pre-Hispanic beads and ceramics from Huanchaco by physical techniques and methods&lt;/strong&gt;&lt;/p&gt;</text>
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                <text>The present study is concerned with the characterization of archaeological materials of beads and ceramics, from the archaeological sites "Iglesia Colonial" and "Pampa La Cruz" of Huanchaco, respectively. The beads of "Iglesia Colonial" were recorded in funerary contexts of the Chimu Inca Period (1450-1532 A.D.) and Early Colonial Period (1532-1650 A.D.). The importance of studying this site lies in understanding the evolution of human occupation between the Inca transition and the arrival of the Spaniards to the north coast of Peru. In the &amp;ldquo;Pampa La Cruz&amp;rdquo; site, tombs containing beads and ceramic vessels prepared with the decorative technique of &amp;ldquo;the negative" were discovered. In this work fragments of the ceramics of this site were investigated, its mineralogical composition was determined qualitatively and quantitatively. This information would help to identify the possible source of clays used for the preparation of the vessels, which, in turn, could help determine if the vessels came from various places, or if the site's inhabitants themselves processed them.</text>
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                <text>El presente estudio est&amp;aacute; referido a la caracterizaci&amp;oacute;n de materiales arqueol&amp;oacute;gicos de cuentas y cer&amp;aacute;micas, provenientes de los sitios arqueol&amp;oacute;gicos &amp;ldquo;Iglesia Colonial&amp;rdquo; y &amp;ldquo;Pampa La Cruz&amp;rdquo; de Huanchaco, respectivamente. Las cuentas de &amp;ldquo;Iglesia Colonial&amp;rdquo; fueron registradas en contextos funerarios del Per&amp;iacute;odo Chimu Inca (1450-1532 d.C.) y Colonial Temprano (1532-1650 d.C.). La importancia de estudiar este sitio radica en entender c&amp;oacute;mo se dio la ocupaci&amp;oacute;n humana entre la transici&amp;oacute;n Inca y la llegada de los Espa&amp;ntilde;oles a la costa norte del Per&amp;uacute;. En el sitio &amp;ldquo;Pampa La Cruz&amp;rdquo; fueron descubiertas tumbas conteniendo cuentas y vasijas de cer&amp;aacute;mica con la t&amp;eacute;cnica decorativa del &amp;ldquo;negativo&amp;rdquo;. En este trabajo fragmentos de cer&amp;aacute;mica de este sitio fueron investigados, su composici&amp;oacute;n mineral&amp;oacute;gica fue determinada cualitativa y cuantitativamente. Esta informaci&amp;oacute;n contribuir&amp;iacute;a a identificar la posible fuente de arcillas utilizadas para la preparaci&amp;oacute;n de las vasijas, lo que, a su vez, podr&amp;iacute;a ayudar a determinar si es que las vasijas proven&amp;iacute;an de varios lugares, o si los mismos pobladores del sitio las procesaban.</text>
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                <text>&lt;strong&gt;Zeballos Vel&amp;aacute;squez, Elvira&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Prieto, Gabriel&lt;/strong&gt;</text>
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                <text>Revista Mat&amp;eacute;ria. v.25, no 1, 2020. --p. 1-10</text>
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                <text>Rede Latino-Americana de Materiais</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt; (Por favor lea este aviso antes de abrir los documentos u objetos)&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho de autor &lt;/strong&gt;sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>On-line&amp;nbsp;version&amp;nbsp;ISSN 1517-7076</text>
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                <text>&lt;strong&gt;11C-Labeling of a flavanone extracted from a South American native species for evaluation of its interaction with GSK-3β&lt;/strong&gt;</text>
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                <text>Natural products play a crucial role in drug discovery, primarily due to their structural complexity. The prenylated flavanone glabranin ((S)-5,7-dihydroxy-8-(3-methylbut- 2-en-1-yl)-2-phenylchroman-4-one), isolated from the Dalea elegans plant species, has demonstrated neuroprotective effects, attributed to its inhibition of GSK-3β, as per our previous in silico studies. Given the enzyme’s diverse functions and its potential as a target for neurodegenerative diseases, our group synthesized and evaluated an 11C-labeled derivative of glabranin. We present its in vitro biological activity, including IC50, neuronal uptake in Alzheimer’s-affected brain regions, key physicochemical properties, and animal studies. This study confirms [11C]FLA’s interaction with GSK-3β in vitro, highlighting the potential of radiotracers in bioactive compound research</text>
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                <text>Molecules, v. 30, n°4, 2025. -- e874</text>
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                <text>2025</text>
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            <description>Information about rights held in and over the resource</description>
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                <text>&lt;p&gt;&lt;strong&gt;Información sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;La legislación uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creación literaria, científica o artística, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeción a lo establecido por el derecho común y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptación de las siguientes condiciones de uso: Este documento es únicamente para usos privados enmarcados en actividades de investigación y docencia. No se autoriza su reproducción con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilización o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Nanoencapsulation may improve antimicrobial activity of nisin when applied on food systems such as lean beef. Nisin-loaded nanoparticles were prepared by alginate ionic gelation and further complexation with chitosan. A 3-factor, 3-level Box-Behnken experimental design and response surface methodology were used to optimize the formulation. Nanoparticles had an encapsulation efficiency of 36.1 &amp;plusmn; 0.6%, a z-average of 66.4 &amp;plusmn; 8.9 nm and a zeta potential of &amp;minus;31.7 &amp;plusmn; 2.6 mV. Transmission electron microscopy and atomic force microscopy observations confirmed particle size found by dynamic light scattering. Also, Raman spectroscopy analyses and zeta potential measurements showed ionic interactions between nisin and alginate. In vitro assessment of inhibition of Listeria monocytogenes growth at 4 &amp;deg;C indicated sustained antimicrobial activity of nisin-loaded nanoparticles for 21 days. Furthermore, encapsulated nisin was able to inhibit L. monocytogenes growth in vacuum-sealed, refrigerated beef samples for 10 days when applied at 400 IU/g and for 24 days when applied at 800 IU/g, while free nisin controlled microbial growth for only 4 and 17 days respectively. In sum, we describe the application of experimental design tools to produce nisin-loaded nanoparticles that may be used in the food industry to control microbial growth and hence extend the shelf-life of lean beef.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Desarrollo de pel&amp;iacute;cula comestible biopolim&amp;eacute;rica con incorporaci&amp;oacute;n de nanopart&amp;iacute;culas bioactivas de potencial aplicaci&amp;oacute;n en productos alimentarios&lt;/strong&gt;</text>
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                <text>CIENCIAS DE LOS ALIMENTOS</text>
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                <text>Los envases alimentarios activos pueden ser dise&amp;ntilde;ados para reducir y controlar efectivamente la aparici&amp;oacute;n de microorganismos pat&amp;oacute;genos y de deterioro, y por ende contribuir a la inocuidad y a prolongar la vida &amp;uacute;til de los alimentos. Una alternativa de creciente inter&amp;eacute;s dentro del &amp;aacute;rea de envasado es el desarrollo de pel&amp;iacute;culas y recubrimientos comestibles y biodegradables a partir de productos naturales. Debido a sus propiedades &amp;uacute;nicas, los biopol&amp;iacute;meros tales como el quitosano (CS) pueden ser utilizados como componentes principales de pel&amp;iacute;culas y recubrimientos. En particular, las pel&amp;iacute;culas biopolim&amp;eacute;ricas pueden contener diversos aditivos para mejorar su funcionalidad, tales como agentes antimicrobianos. La nisina (NIS) es una bacteriocina producida por Lactococcus lactis que presenta actividad antibacteriana contra Listeria monocytogenes y es la &amp;uacute;nica bacteriocina Generalmente Reconocida Como Segura (GRAS). Sin embargo, su actividad en alimentos est&amp;aacute; limitada por varios factores por lo que es posible recurrir a la utilizaci&amp;oacute;n de t&amp;eacute;cnicas de nanoencapsulaci&amp;oacute;n para preservar la actividad y controlar la liberaci&amp;oacute;n de dicho compuesto.</text>
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                <text>The objective of this work was to investigate the effect of the addition of carboxymethyl chitosan on the structural properties and antilisterial activity of nisin-incorporated chitosan films. Chitosan and carboxymethyl chitosan solutions were prepared with different mass ratios and bacteriocin nisin was added (0, 1000 and 6000 IU/ml). Filmogenic solutions were cast, dried and their physico-chemical and antimicrobial properties were investigated. For the same chitosan/carboxymethyl chitosan mass ratio, the addition of NIS at 6000 IU/ml led to changes in the macro- and microstructure, as well as in physico-chemical properties of films. On the other hand, carboxymethyl chitosan had a plasticizing effect and enhanced the distribution of the bacteriocin within the biopolymer matrix. Moreover, nisin-incorporated blend films of chitosan and carboxymethyl chitosan were more effective against Listeria monocytogenes than their pure chitosan counterparts. This study showed that different formulations of nisin-incorporated composite films of chitosan and carboxymethyl chitosan may provide options for developing bioactive packaging to improve food safety.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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                <text>The progress in the preparation of new electrode surfaces by electrochemical treatments exhibiting high faradaic efficiencies towards industrial electrocatalytic processes has gained more attention in today&amp;rsquo;s scientific community. Most of the papers report new catalysts dispersed on different substrates, but some fundamental studies required for electrochemical and physical characterizations are sometimes forgotten. In this paper, we make a full staging of two electrochemical treatments that can be conducted to enhance the electrocatalytic activity of platinum surfaces, such as, electrofacetting through square wave potential programs and constant cathodic polarizations in the net hydrogen evolution region. The cathodic treatment applied at &amp;minus;2V clearly develops (111) stepped planes similarly to the electrofacetting performed after applying the square wave program between 1.40V and 0.70 V at 2.5 kHz. The X-ray diffraction patterns of both surfaces as well as on other electrofacetted platinum electrodes are obtained for comparison purposes. Moreover, the electrocatalytic activity towards methanol electrooxidation also exhibits equivalent coulombic efficiencies and 200% higher than on polycrystalline platinum as demonstrated by linear sweep voltammetry and potentiostatic current decays.</text>
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                <text>International Journal of Electrochemistry v. 2011, no. ID 289032, 2011. -- p. 1-9</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p style="margin-bottom: 0cm;"&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>The effects of I&amp;ndash;adsorption on the electrodeposition (under and overpotential deposition) of Cu on polycrystalline Pd electrodes were studied in dilute perchloric acid solutions at 18&amp;deg;C. It had been found that Cu underpotential deposition on polycrystalline Pd exhibits different potentiodynamic features, which are characteristic of defined crystallographic planes of Pd. However, these features varied when the voltammograms were performed in the presence of strongly adsorbable anions, such as I&amp;ndash;. In spite of having found a partial inhibition of the Cu voltammetric features in the presence of I&amp;ndash;, we calculated integer numbers in the electron transfer to Cu2+and I&amp;ndash;ions. The change in the values of Cu massive deposition potential due to the presence of I&amp;ndash;was caused by the appearence of a new electrode, that is, the Cu/CuI/I&amp;ndash;interface.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Electrochemical behavior and semiempirical approach to the electroadsorption of 3-buten-2-one and 2-butanone on platinum.&lt;/strong&gt;</text>
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                <text>The electroadsorption of 3-buten-2-one was studied on polycrystalline and faceted Pt electrodes in aqueous 0.5 M H(2)SO(4) between 20 and 70 degrees C using voltammetric and transient techniques. The largest values of anodic charge densities in stripping experiments were observed at the potential of zero charge of the Pt/acid interface (ca. 0.20 V), that is, 550, 680, and 720 &amp;micro;C cm(-2), on polycrystalline and (111)- and (100)-faceted electrodes, respectively. The anodic and cathodic strippings of 3-buten-2-one showed the formation of at least two residues with different electrochemical behavior. For comparison cyclic voltammetries and current transients of 2-butanone on Pt were also studied. To get a deeper insight into the adsorption configurations of 3-buten-2-one and 2-butanone, the extended H&amp;uuml;ckel molecular orbital methodology was used to predict adsorption geometries and binding energies on simulated Pt(100) and Pt(111) single-crystal surfaces. At equilibrium potentials, two types of adsorbed species were recognized, a planar 3-buten-2-one formed by the interaction of carbonyl and alkene groups and adsorbates coming from the single interaction of the &amp;gt;C&amp;amp;dbond;O moiety for both 3-buten-2-one and 2-butanone. At simulated positive potentials, 3-buten-2-one adsorption occurred on Pt(111) and Pt(100) clusters through the pi-orbitals of the &amp;gt;C&amp;amp;dbond;C&amp;lt; moiety, whereas at negative potentials 3-buten-2-one was adsorbed via &amp;micro;-bridging or di-varsigma configuration(s)</text>
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                <text>Journal of Colloid and Interface Science v. 219, no. 2, 1999. -- p. 260</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;A DEMS study of the electroreduction and oxidation of 3-buten-2-butanone adsorbates on platinum in sulphuric solutions.&lt;/strong&gt;</text>
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                <text>The electrochemical adsorption characteristics of 3-buten-2-one and 2-butanone on porous platinum electrodes were investigated by differential electrochemical mass spectrometry (DEMS) in aqueous 0.5 M H2SO4. The study was conducted through the oxidation and reduction of residues formed at different adsorption potentials (Ead). The maximum adsorption for both organic substances was observed at the potential of zero charge of the interface, that is, ca 0.20 V. At this potential an adsorbate species with the C&amp;ndash;O bond lying parallel to the surface is proposed. The sole oxidation product for both molecules was carbon dioxide. Anodic current transients were detected for 3-buten-2-one at adsorption potentials higher than 0.20 V. Between 0.40 and 0.60 V, it is possible to admit a 1&amp;ndash;3e&amp;minus; loss during adsorption with a progressive fragmentation of the original molecule at increasing Ead. After three cycles in the H-adatom region, about 75% of the 3-buten-2-one adsorbate is desorbed; the main products being butane, 1-butene and propane. The ratio of these products depends on Ead, as is expected for the fragmentation of the molecule upon increasing potentials. On the other hand, 2-butanone was adsorbed in the 0.10&amp;ndash;0.60 V potential range without current transients associated with the dissociative reactions of the molecule. The surface coverage diminished drastically at both sides of the maximum adsorption (0.20 V). Butane was the main reduction product of 2-butanone.</text>
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                <text>Journal of Electroanalytical Chemistry v. 454, no. 1/2, 1998. -- p. 161</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Adsorption configurations of ethylene and acetylene on gold.&lt;/strong&gt;</text>
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                <text>An improved extended H&amp;uuml;ckel molecular orbital study was conducted to predict the adsorbate configuration of ethylene and acetylene on Au(100) and Au(111) single crystal cluster surfaces at different simulated electric potentials. Three adsorbed configurations on both cluster surfaces were found for ethylene and acetylene, i.e. &amp;pi;, di-&amp;sigma; and &amp;mu;-bridging species, whose relative contributions to the total organic surface coverage depend on the electric potential. Acetylene is chemisorbed on gold in a &amp;pi;-bonded mode when a positively charged surface is simulated, whereas di-&amp;sigma; and &amp;mu;-bridging state are the most likely adsorption modes at negative electric potentials, the binding energies on Au(100) being larger than those of Au(111) clusters. Ethylene, on the other hand, is physisorbed on gold at equilibrium and positive electric potentials, however the chemisorption of the molecule is achieved when a negatively charged surface is simulated. Adsorption of ethylene at potentials below that of zero charge of the gold solution interface was observed. The anodic stripping of adsorbed ethylene at potentials lower than 0.20 V in 1 M H2SO4 (0.25 V in 1 M HClO4) exhibits two residues, in the double layer and in the gold oxide region. On the other hand, the adsorption of acetylene took place in two potential regions, one coinciding with the ethylene adsorption domain, and the other involving potential values positive to that of zero charge.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Journal of Electroanalytical Chemistry v. 415, no. 1/2, 1996. -- p. 165-167</text>
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              <elementText elementTextId="330714">
                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Extended Hueckel molecular orbital calculations for the adsorption of H-atoms in a simulated aqueous electrochemical environment on Pt(111) and Pt(100) clusters were made. Different adsorbate configurations were considered. H-atom adsorption on hollow sites coadsorbed with an on top OH-species for Pt(111), and H-atom adsorption on bridge sites for Pt(100) are favoured. At potentials lower than the hydrogen electrode equilibrium potential, H-adatom configurations involving subsurface Pt atoms can also be formed. For both Pt(111) and Pt(100), these structures are probably related to species involved in the H-atom electrosorption and hydrogen evolution reaction.</text>
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                <text>&lt;strong&gt;Temperature dependence of kinetics parameters related to oxygen electroreduction in acid solutions on platinum electrodes.&lt;/strong&gt;</text>
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                <text>The oxygen electroreduction reaction (OERR) kinetics at (111)- and (100)-type Pt electrodes has been studied in aqueous 1.0 M H2SO4 solutions in the 8&amp;ndash;62&amp;deg;C range. On both Pt electrodes and at all temperatures, two Tafel regions have been observed. The Tafel slope in the low current density range is &amp;minus;0.053 &amp;plusmn; 0.005 V decade&amp;minus;1, irrespective of temperature and the surface texture of the electrode. For (111)-type Pt, the Tafel slope in the high current density range increases with temperature, approaching the &amp;minus;2.303(2RT/F) ratio, whereas for (100)-type Pt, it reaches a temperature-independent value equal to &amp;minus;0.165 &amp;plusmn; 0.003 V decade&amp;minus;1. Temperature dependences of OERR Tafel slopes on both types of Pt electrodes offer the possibility of further insights into the mechanism of the reaction, through the interpretation of both the adsorption enthalpy and entropy of intermediates produced along the OERR. Compensation effects, involving activation enthalpy and entropy variations with the applied potential, are also considered to account for experimental data.</text>
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                <text>Electrochimica acta v. 39 , no. 13, 1994. -- p. 1951-1959</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;p&gt;&lt;strong&gt;The electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution.&lt;/strong&gt;&lt;/p&gt;&#13;
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                <text>The oxygen electroreduction reaction was studied on two different preferentially oriented ((111)-type and (100)-type and on a conventional polycrystalline (PC) platinum rotating disc electrodes in acid solutions at 30 &amp;deg;C. At low overpotentials, Tafel lines of &amp;minus;0.060 V decade&amp;minus;1 were obtained on the three electrodes in oxygen-saturated 1.0m H2SO4 and 1.0m H2SO4 + y m K2SO4 (0 ⩽y ⩽ 1). At high over-potentials the usual Tafel slope of -0.120V decade&amp;minus;1 was observed on both (111)-type and PC platinum electrodes in 1.0m H2SO4, whereas a slope of &amp;minus;0.165V decade&amp;minus;1 was found on (100)-type platinum. In oxygen-saturated 1.0m H2SO4 the surface coverage by O-containing adsorbates on (100)-type platinum was greater than on both (111)-type and PC platinum. Rotating ring-disc electrode data showed that a higher amount of H2O2 was produced on (100)-type platinum than on the other platinum surfaces. The overpotential against current density plots are influenced by the anion concentration depending on the type of preferentially oriented platinum.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt; Kinetics and mechanism of the electrochemical reduction of molecular oxygen on platinum in KOH:influence of preferred crystallographic orientation.&lt;/strong&gt;</text>
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                <text>The oxygen electroreduction reaction has been studied at both preferred oriented and conventional polycrystalline platinum rotating disc electrodes in x m KOH (0.05 ⩽ x ⩽ 3.0) aqueous solutions under oxygen saturation at 25&amp;deg;C. At low current densities, Tafel lines with slope -0.060 V decade&amp;minus;1 have been obtained at all platinum electrodes. At high current densities, higher Tafel slopes ranging from -0.18 to -0.40 V decade&amp;minus;1 have been observed, depending on the type of preferred oriented Pt and KOH concentration. Rotating ring-disc electrode data have shown that a higher amount of H2O2 is produced on one type of preferred oriented surface at all KOH concentrations. A complex reaction scheme has been used to evaluate the electrochemical rate constants of the reaction steps at three platinum electrodes.</text>
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                <text>Journal of applied electrochemistry v. 24, no. 6, 1994. -- p. 531-541</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>AB2 alloys have been extensively studied as Ni-MH battery anodes. In the hydriding process, hydrogen diffusion inside the crystal lattice is the determining step, so a comparison between gas phase and electrochemical environment was carried out. As concern, we have found structural changes as a consequence of hydriding in terms of segregation of different stable phases and variations in unit cell parameters in each alloy. Maximum hydrogen storage capacity and hydrogen molar volume for studied alloys were evaluated by PCT curves at different temperatures. Resulting values were compared with electrochemical PCT (ECT plots). Results obtained for both methods were similar, with a hydrogen molar volume value close to 30 cm3 mol-1 being higher for AB2M0 in accordance with the reported capacity values. Diffusion time constants were determined from GITT, achieved data were similar to previously reported by EIS and HRD. AB2M1 alloy showed the best kinetic behavior, depicting a time constant value an order of magnitude lower than AB2M0. This fact could be attributed to the diffusion coefficient and/or the hydrogen diffusion length mean path. No significant differences in thermodynamic parameters were observed between both alloys, therefore, the diffusion coefficients should be similar. Thus, differences in time diffusion constants were attributed to dissimilar mean lattice diffusion paths associated with changes in crystalline structures as a result of the hydriding process.&#13;
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                <text>Journal of Electroanalytical Chemistry v. 879, 2020. -- p. 1-17.--e.114781&#13;
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                <text>The development of new electrochemical immunosensors for the detection of environmental contaminants is of great interest due to their simplicity, high sensitivity, and extended analytical range. Because of the antibody is immobilized on the electrode, it is important to determine its loss of reactivity after immobilization. In this work, two aspects were addressed. First, we developed a new methodology based on electrochemical impedance (EI) to determine the kinetic parameters associated with immunoreactions carried out on the electrode. Second, an electrochemical immunosensor based on electrochemical impedance spectroscopy (EIE) was developed to determine microcystin-LR in drinking water samples. Microcystin-LR determination was based on a label-free non-competitive immunoassay. The electrochemical immunosensor shows a limit of detection (LOD) of 33 pg mL�1 (3.32 � 10�11 mol L�1 or 0.033 mg L�1) which is well below the WHO guideline recommendation of 1 mg L�1 and 40 times better than the LOD obtained using the same antibody in an optimized conventional competitive ELISA assay. In addition, an acceptable accuracy, with recovery percentages close to 100% were found. The label-free immunosensor is a valuable tool to monitor microcystin-LR in drinking water samples and the environment.&#13;
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            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
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                <text>&lt;strong&gt;Boffadossi, Micaela &lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Di Tocco, Aylen&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Lassabe, Gabriel&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Pirez-Schirmer, Macarena&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Robledo, Sebasti&amp;aacute;n Noel&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Fern&amp;aacute;ndez, H&amp;eacute;ctor&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Zon, Mar&amp;iacute;a Alicia&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Gonz&amp;aacute;lez Sapienza, Gualberto&lt;/strong&gt;&#13;
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                <text>&lt;strong&gt;Ar&amp;eacute;valo, Fernando Javier&lt;/strong&gt;&#13;
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            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="562521">
                <text>Electrochimica Acta v. 153, 2020. -- p. 1-8.--e136621&#13;
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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              <elementText elementTextId="562522">
                <text>Elsevier&#13;
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="562523">
                <text>2020&#13;
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="562524">
                <text>&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt; (Por favor lea este aviso antes de abrir los documentos u objetos)&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho de autor&lt;/strong&gt;sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&#13;
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            <name>Format</name>
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                <text>Pdf&#13;
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                <text>Ingl&amp;eacute;s&#13;
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                <text>Art&amp;iacute;culo&#13;
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                <text>https://doi.org/10.1016/j.electacta.2020.136621&#13;
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        <name>Electroquímica</name>
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        <name>Inmunoensayo</name>
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        <name>Microcistina</name>
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