scholarly journals Are N-methyl groups of Tetramethylurea (TMU) Hydrophobic? A composition and temperature-dependent fluorescence spectroscopic investigation of TMU/water binary mixtures

2016 ◽  
Vol 128 (5) ◽  
pp. 753-761 ◽  
Author(s):  
SANDIPA INDRA ◽  
RANJIT BISWAS
2018 ◽  
Vol 122 (32) ◽  
pp. 7884-7894 ◽  
Author(s):  
Samuel Lenton ◽  
Natasha H. Rhys ◽  
James J. Towey ◽  
Alan K. Soper ◽  
Lorna Dougan

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1059
Author(s):  
Sanghun Lee ◽  
Curtis W. Frank ◽  
Do Y. Yoon

Molecular dynamics simulations of free-standing thin films of neat melts of polyethylene (PE) chains up to C150H302 and their binary mixtures with n-C13H28 are performed employing a united atom model. We estimate the surface tension values of PE melts from the atomic virial tensor over a range of temperatures, which are in good agreement with experimental results. Compared with short n-alkane systems, there is an enhanced surface segregation of methyl chain ends in longer PE chains. Moreover, the methyl groups become more segregated in the surface region with decreasing temperature, leading to the conclusion that the surface-segregation of methyl chain ends mainly arises from the enthalpic origin attributed to the lower cohesive energy density of terminal methyl groups. In the mixtures of two different chain lengths, the shorter chains are more likely to be found in the surface region, and this molecular segregation in moderately asymmetric mixtures in the chain length (C13H28 + C44H90) is dominated by the enthalpic effect of methyl chain ends. Such molecular segregation is further enhanced and dominated by the entropic effect of conformational constraints in the surface for the highly asymmetric mixtures containing long polymer chains (C13H28 + C150H3020). The estimated surface tension values of the mixtures are consistent with the observed molecular segregation characteristics. Despite this molecular segregation, the normalized density of methyl chain ends of the longer chain is more strongly enhanced, as compared with the all-segment density of the longer chain itself, in the surface region of melt mixtures. In addition, the molecular segregation results in higher order parameter of the shorter-chain segments at the surface and deeper persistence of surface-induced segmental order into the film for the longer chains, as compared with those in neat melt films.


2017 ◽  
Vol 41 (17) ◽  
pp. 9330-9337 ◽  
Author(s):  
Man Yang ◽  
Liyan Ma ◽  
Kongshuang Zhao

A dielectric spectroscopy study on the binary mixtures of the ionic liquid (IL) 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4]) and four kinds of alcohols as a function of temperature was carried out over a frequency range of 100 MHz to 20 GHz.


Author(s):  
Th.D. Ferris ◽  
Th.C. Farrar

Concentration and temperature dependent measurements of the hydroxyl proton chemical shift and deuterium longitudinal relaxation time of binary mixtures of ethanol and carbon tetrachloride were made over a 60 degree temperature range. Concentrations ranged from 1.02 mole percent to neat ethanol.


2017 ◽  
Vol 82 (10) ◽  
pp. 1155-1174 ◽  
Author(s):  
Rebecca Andrade ◽  
Alberto Carreras ◽  
Miguel Iglesias

Two binary mixtures of protic ionic liquids comprising formate, acetate and propionate anions and 2-hydroxyethyl ammonium, bis(2-hydroxyethyl) ammonium and tris(2-hydroxyethyl) ammonium cations have been studied in terms of volumetric and acoustic properties as a function of temperature. The corresponding derived properties have been computed from the experimental data and fitted to temperature dependent Redlich?Kister and Redlich? ?Mayer equations; accurate results being obtained. Other properties such as intermolecular free length, acoustic impedance, geometrical volume, collision factor and isothermal coefficient of pressure excess molar enthalpy were computed due to their importance in the study of specific molecular interactions. The new experimental data were used to test the prediction capability of different models for density (Mchaweh?Nasrifar?Moshfeghian (MNM) model and the modified Heller temperature dependent equation (MHE)) and ultrasonic velocity (different empirical equations, collision factor theory (CFT) and free length theory (FLT)). The high non-ideality of these mixtures points to strong contractive behaviour at any temperature and composition. The obtained results indicate that ionic liquid interactions into mixture are stronger than in the ionic pure components for both mixtures at any studied condition. Despite the strong ion interaction, the tested models showed, at least, the qualitative prediction capability.


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