Mostrar el registro sencillo del ítem

dc.contributor.author
Conde Garrido, Juan Manuel  
dc.contributor.author
Silveyra, Josefina María  
dc.contributor.author
Ureña, Maria Andrea  
dc.date.available
2017-07-07T21:53:18Z  
dc.date.issued
2016-02  
dc.identifier.citation
Conde Garrido, Juan Manuel; Silveyra, Josefina María; Ureña, Maria Andrea; Multi-ion and pH sensitivity of AgGeSe ion selective electrodes; Elsevier; Journal of Physics and Chemistry of Solids; 89; 2-2016; 115-119  
dc.identifier.issn
0022-3697  
dc.identifier.uri
http://hdl.handle.net/11336/19948  
dc.description.abstract
Many chalcogenide glasses have been found to combine benefits such as good chemical durability, selectivity, and reproducibility for applications as solid-state sensitive membranes of ion selective electrodes (ISEs). In previous works, we have shown that ISEs with ionic conductive AgGeSe membranes have good sensitivity to Ag+ ions. In the present work, we explore the Agx(Ge0.25Se0.75)100−x, 10≤x≤30 (at%) system as candidate for ISEs applications detecting several other ions (K+, Mg2+, Cr3+, Fe3+, Ni2+, Cd2+, Hg2+, and Pb2+). We evaluated ISEs fabricated with bulk as well as with thin film membranes. We found no dependence of the sensing properties on the Ag content of the ionic conductive membranes. Thin films exhibited the same properties than bulk membranes, indicating that these chalcogenide glasses have great potential for miniaturization. The ISEs showed a high response (Nernstian or super-Nernstian) to the presence of Hg2+, Pb2+, and Fe3+, a low response (sub-Nernstian) to the presence of Cr3+, and a total lack of response to the presence of Cd2+, Ni2+, Mg2+, and K+. We also tested how the pH of the solution affected the response of the ISEs. The potentials of the ISEs were practically constant in neutral or acidic solutions, while decreased drastically in basic solutions when the primary ion was not present. The latter phenomenon was caused by the slow dissolution of the membrane into the solution, meaning that long-term basic environments should be avoided for these ISEs. We concluded that ISEs with ionic conductive AgGeSe membranes are good candidates to integrate multi-electrode systems.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Ise  
dc.subject
Chalcogenide Glass  
dc.subject
Thin Films  
dc.subject
Selectivity  
dc.subject
Electronic Tongue  
dc.subject.classification
Otras Ingeniería de los Materiales  
dc.subject.classification
Ingeniería de los Materiales  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Multi-ion and pH sensitivity of AgGeSe ion selective electrodes  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-07-06T18:33:56Z  
dc.journal.volume
89  
dc.journal.pagination
115-119  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Ámsterdam  
dc.description.fil
Fil: Conde Garrido, Juan Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Tecnologías y Ciencias de la Ingeniería "Hilario Fernández Long". Universidad de Buenos Aires. Facultad de Ingeniería. Instituto de Tecnologías y Ciencias de la Ingeniería "Hilario Fernández Long"; Argentina. Universidad de Buenos Aires. Facultad de Ingenieria. Departamento de Fisica. Laboratorio de Sólidos Amorfos; Argentina  
dc.description.fil
Fil: Silveyra, Josefina María. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Tecnologías y Ciencias de la Ingeniería "Hilario Fernández Long". Universidad de Buenos Aires. Facultad de Ingeniería. Instituto de Tecnologías y Ciencias de la Ingeniería "Hilario Fernández Long"; Argentina. Universidad de Buenos Aires. Facultad de Ingenieria. Departamento de Fisica. Laboratorio de Sólidos Amorfos; Argentina  
dc.description.fil
Fil: Ureña, Maria Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Tecnologías y Ciencias de la Ingeniería "Hilario Fernández Long". Universidad de Buenos Aires. Facultad de Ingeniería. Instituto de Tecnologías y Ciencias de la Ingeniería "Hilario Fernández Long"; Argentina. Universidad de Buenos Aires. Facultad de Ingenieria. Departamento de Fisica. Laboratorio de Sólidos Amorfos; Argentina  
dc.journal.title
Journal of Physics and Chemistry of Solids  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0022369715300834  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.jpcs.2015.10.015