Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marika Yokota"'
Publikováno v:
Polymer Journal. 54:259-267
We estimated the configurational heat capacity for 21 types of polymers above the glass transition temperature (Tg) using molecular vibration analysis. The polymers for which the configurational heat capacity was determined are listed as follows: six
Publikováno v:
Polymer Journal. 54:33-39
In this study, we investigated the functions that reproduce the configurational heat capacity (Cconfig) above the glass transition temperature for polystyrene (PS), polyisobutylene (PIB), and their oligomers. The results show that Cconfig can be well
Publikováno v:
Polymer Journal. 53:1031-1036
In this study, the absolute values for the configurational heat capacity of polyisobutylene (PIB), isobutane (which corresponds to the monomer of PIB), and 2,2,4-isomethylpentane (which corresponds to the dimer of PIB) were estimated based on the ass
Autor:
Marika Yokota, Itaru Tsukushi
Publikováno v:
Polymer Journal. 52:1113-1120
This study predicts the absolute values of heat capacities from the molecular formula per monomer for main-chain-type polymers below the glass transition temperature. The frequencies of the skeletal and group-vibration modes are calculated using the
Autor:
Itaru Tsukushi, Marika Yokota
Publikováno v:
Polymer Journal. 52:1103-1111
We evaluated the absolute values of the heat capacity of polymer solids composed of polyesters and poly(oxide)s below the glass transition temperature. The frequencies of the skeletal and group-vibration modes were calculated by the Tarasov and Einst
Publikováno v:
Polymer Journal. 52:765-774
Despite being a useful variable for the quantitative analysis of the thermodynamic properties of polymers, the absolute value of heat capacity remains poorly understood for amorphous polymers. This study evaluates the absolute values of the heat capa
Publikováno v:
Polymer Journal. 52:575-580
In this work, we analyze the absolute heat capacity below the glass-transition temperature Tg for two types of amorphous polystyrene with differing low-molecular weights. Both amorphous polystyrenes have excess heat capacities that cannot be reproduc
Publikováno v:
Thermochimica Acta. 720:179427