Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46389
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSpah, D C-
dc.contributor.authorSingh, K C-
dc.contributor.authorKalra, K C-
dc.date.accessioned2019-03-22T07:22:26Z-
dc.date.available2019-03-22T07:22:26Z-
dc.date.issued1990-06-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46389-
dc.description546-551en_US
dc.description.abstractThe excess volumes and enthalpies of mixing of binary mixtures of 1,2-dibromoethane with benzene, toluene, o-xylene, m-xylene and p-xylene have been measured experimentally over the whole composition range at 308.15K. The data have been explained qualitatively on the basis of electron-donor/ acceptor interactions between 1,2-dibromoethane and the aromatic hydrocarbons and also in terms of the loss of favourable orientational order of the pure components. Flory's theory is not able to predict correctly the VE and HE values of systems studied. However, the Sanchez and Lacombe. Theory correctly predicts the change of sign of HE values with change of mole fraction. Calculated HE by this theory is of the same order as experimental HE. Calculated VE values show relatively poor agreement with the corresponding experimental VE values.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.29A(06) [June 1990]en_US
dc.titleThermodynamics of molecular interactions of 1,2-dibromoethane + aromatic hydrocarbon mixtures at 308.15Ken_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.29A(06) [June 1990]

Files in This Item:
File Description SizeFormat 
IJCA 29A(6) 546-551.pdf411.5 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.