Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/48886
Campo DC Valoridioma
dc.contributor.authorGarcía, Begoñaen_US
dc.contributor.authorAlcalde, Rafaelen_US
dc.contributor.authorLeal, José M.en_US
dc.contributor.authorTrenzado, José L.en_US
dc.date.accessioned2018-11-24T01:51:03Z-
dc.date.available2018-11-24T01:51:03Z-
dc.date.issued1997en_US
dc.identifier.issn0894-3230en_US
dc.identifier.urihttp://hdl.handle.net/10553/48886-
dc.description.abstractDensities were measured for the N‐methylformamide–(C1–C10)alkan‐1‐ol and N,N‐dimethylformamide–(C1–C10)alkan‐1‐ol solvent mixtures at 298·15 K over the whole miscibility range (0<X1<1). The excess volumes (VE), which are discussed in terms of intermolecular interactions, are negative for the mixtures with the smallest alkanols in the series and increase with increase in the chain length. Comparison with other amide–alcohol mixtures previously investigated (formamide and pyrrolidin‐2‐one) indicates that the excess volumes are strongly influenced by the size of the alcohol and to a lesser extent by the nature of the amide. In contrast with the amide–water system, neither the amide size nor its degree of substitution plays an important role in the amide–alcohol systems investigated.en_US
dc.languageengen_US
dc.publisher0894-3230-
dc.relation.ispartofJournal of Physical Organic Chemistryen_US
dc.sourceJournal of Physical Organic Chemistry [ISSN 0894-3230], v. 10, p. 138-144en_US
dc.subjectInvestigaciónen_US
dc.subject.otherAmide–alcohol solvent systemsen_US
dc.subject.otherDensitiesen_US
dc.subject.otherVolumetric behaviouren_US
dc.titleVolumetric behaviour of n-methylformamide-(c1-c10)alkan-1-ol and N,N-dimethylformamide-(c1-c10)alkan-1-ol solvent systemsen_US
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1002/(SICI)1099-1395(199703)10:3<138::AID-POC872>3.0.CO;2-Den_US
dc.identifier.scopus0002331542-
dc.identifier.isiA1997XF14800002
dc.contributor.authorscopusid23113399400-
dc.contributor.authorscopusid57204665125-
dc.contributor.authorscopusid24547015200-
dc.contributor.authorscopusid6602495462-
dc.description.lastpage144-
dc.description.firstpage138-
dc.relation.volume10-
dc.investigacionCienciasen_US
dc.type2Artículoen_US
dc.contributor.daisngid273235
dc.contributor.daisngid9153108
dc.contributor.daisngid74944
dc.contributor.daisngid2373764
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Garcia, B
dc.contributor.wosstandardWOS:Alcalde, R
dc.contributor.wosstandardWOS:Leal, JM
dc.contributor.wosstandardWOS:Trenzado, JL
dc.date.coverdateMarzo 1997
dc.identifier.ulpgces
dc.description.jcr1,118
dc.description.jcrqQ3
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR Termofísica de Líquidos y Calorimetría-
crisitem.author.deptDepartamento de Física-
crisitem.author.orcid0000-0001-9858-1453-
crisitem.author.parentorgDepartamento de Física-
crisitem.author.fullNameTrenzado Diepa, José Luis-
Colección:Artículos
Vista resumida

Citas SCOPUSTM   

19
actualizado el 24-mar-2024

Citas de WEB OF SCIENCETM
Citations

19
actualizado el 25-feb-2024

Visitas

53
actualizado el 14-ene-2023

Google ScholarTM

Verifica

Altmetric


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.