dc.creatorVargas Fernández, Andrés
dc.creatorSánchez, Marianela
dc.creatorDíaz Soler, Felipe
dc.creatorVásquez Quitral, Patricio
dc.creatorYazdani Pedram, Mehrdad
dc.creatorNeira Carrillo, Andrónico
dc.date.accessioned2020-05-06T19:34:21Z
dc.date.available2020-05-06T19:34:21Z
dc.date.created2020-05-06T19:34:21Z
dc.date.issued2020
dc.identifierCrystal Growth & Design Volume: 20 Issue: 2 Pages: 661-669 ‏ Feb 2020
dc.identifier10.1021/acs.cgd.9b01067
dc.identifierhttps://repositorio.uchile.cl/handle/2250/174455
dc.description.abstractThe electrocrystallization (EC) of calcium oxalate (CaOx) crystals in the presence of multiwalled carbon nanotubes (MWCNTs) functionalized with itaconic acid (IA) and the monoester derivatives mono-methylitaconate or mono-octadecylitaconate, which were used as new IA-ester templates supported on indium tin oxide glass substrate as working electrode, was performed by applying a 9 mA current at 37 and 60 degrees C for 5 min. Under the above EC reaction conditions, a broad variety of CaOx morphologies and crystal forms was found. The morphology control and coexistence of CaOx monohydrate (COM) and CaOx dihydrate was achieved through in vitro EC according to X-ray diffraction spectra. We found that all the functionalized MWCNTs were more efficient inhibitors of CaOx crystallization than the typical citrate model, where MWCNT-IA was the most effective stabilizing template of COM crystals, because carboxylic acid groups of IA moieties in MWCNT-IA would be better Ca2+ ions binding sites than IA ester groups.
dc.languageen
dc.publisherAmer Chemical Soc
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceCrystal Growth & Design
dc.subjectCarbonate
dc.subjectCrystallization
dc.subjectHydroxyapatite
dc.subjectInhibition
dc.subjectDeposition
dc.subjectMorphology
dc.subjectCaco3
dc.subjectOxide
dc.titleEffect of Functionalized Multiwalled CNTs on the Selective Formation of Calcium Oxalate Crystals by Electrocrystallization
dc.typeArtículo de revista


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