CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Application of fast scanning calorimetry to the fusion thermochemistry of low-molecular-weight organic compounds: Fast-crystallizing m-terphenyl heat capacities in a deeply supercooled liquid state
Authors
Lapuk S.
Mukhametzyanov T.
+4 more
Schick C.
Solomonov B.
Yagofarov M.
Ziganshin M.
Publication date
1 January 2018
Publisher
Abstract
© 2018 Elsevier B.V. Fusion enthalpy temperature dependence is related to the difference in heat capacity of the liquid and solid. Below the melting temperature, it is hard to measure the liquid heat capacity using conventional methods due to fast crystallization. Based on an indirect solution calorimetry approach, we previously concluded that the temperature dependence of heat capacities below the melting temperature is the extrapolation of the linear function above it. In this study, we employed a fast scanning calorimetry technique to test the validity of this conclusion. Three compounds were studied: two organic glass formers, benzophenone and o-terphenyl, for which the liquid and supercooled liquid heat capacities were known to be accurately described by a linear function of temperature, and m-terphenyl, which had never been studied in the supercooled liquid state. The results were in good agreement with the literature for liquid benzophenone and o-terphenyl heat capacities above and below the melting temperature. The heat capacity of the supercooled liquid and glassy m-terphenyl was obtained for the first time. The measured molar heat capacity of supercooled liquid m-terphenyl was the linear extrapolation of the temperature dependence of the heat capacity of the melt found in the literature. The molar heat capacity of the solid, the enthalpy and fusion temperature of m-terphenyl were determined by conventional DSC. Kirchhoff's integral, calculated from the measured molar heat capacities of solid and liquid m-terphenyl, was in accordance with the fusion and solution thermochemistry data
Similar works
Full text
Open in the Core reader
Download PDF
Available Versions
Kazan Federal University Digital Repository
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:dspace.kpfu.ru:net/147813
Last time updated on 07/05/2019