Conformational analysis and molecular dynamics of glass-forming aromatic thiacrown ethers

The present work aims to provide insights on recent findings indicating the presence of multiple equilibration mechanisms in physical aging of glasses. To this aim, we have investigated a glass forming polyether, poly(1-4 cyclohexane di-methanol) (PCDM), by following the evolution of the enthalpic state during physical aging by fast scanning calorimetry (FSC). The main results of our study indicate that physical aging persists at temperatures way below the glass transition temperature and, in a narrow temperature range, is characterized by a two steps evolution of the enthalpic state. Altogether, our results indicate that the simple old-standing view of physical aging as triggered by the α relaxation does not hold true when aging is carried out deep in the glassy state.

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Enhanced dielectric properties of high glass transition temperature PDCPD/CNT composites by frontal ring-opening metathesis polymerization

Advanced Composites and Hybrid Materials ◽

10.1007/s42114-021-00287-0 ◽

2021 ◽

Author(s):

Ping Wang ◽

Li Yang ◽

Shang Gao ◽

Xinliang Chen ◽

Tian Cao ◽

...

Keyword(s):

Glass Transition ◽

Transition Temperature ◽

Dielectric Properties ◽

Glass Transition Temperature ◽

Ring Opening ◽

High Glass Transition Temperature ◽

Ring Opening Metathesis Polymerization ◽

Metathesis Polymerization

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Influence of Carbon Nanotube Aspect Ratio on Glass Transition Temperature of Polymers: A Molecular Dynamics Simulation Study

Materials Science Forum ◽

10.4028/www.scientific.net/msf.817.797 ◽

2015 ◽

Vol 817 ◽

pp. 797-802 ◽

Cited By ~ 2

Author(s):

Cai Jiang ◽

Jian Wei Zhang ◽

Shao Feng Lin ◽

Su Ju ◽

Da Zhi Jiang

Keyword(s):

Molecular Dynamics ◽

Glass Transition ◽

Carbon Nanotube ◽

Transition Temperature ◽

Glass Transition Temperature ◽

Aspect Ratio ◽

Epoxy Resin ◽

Md Simulations ◽

Diglycidyl Ether ◽

Dynamics Simulation

Molecular dynamics (MD) simulations on three single walled carbon nanotube (SWCNT) reinforced epoxy resin composites were conducted to study the influence of SWCNT type on the glass transition temperature (Tg) of the composites. The composite matrix is cross-linked epoxy resin based on the epoxy monomers bisphenol A diglycidyl ether (DGEBA) cured by diaminodiphenylmethane (DDM). MD simulations of NPT (constant number of particles, constant pressure and constant temperature) dynamics were carried out to obtain density as a function of temperature for each composite system. The Tg was determined as the temperature corresponding to the discontinuity of plot slopes of the densityvsthe temperature. In order to understand the motion of polymer chain segments above and below the Tg, various energy components and the MSD at various temperatures of the composites were investigated and their roles played in the glass transition process were analyzed. The results show that the Tg of the composites increases with increasing aspect ratio of the embedded SWCNT

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Long-Term Physical (In)Stability of Spray-Dried Amorphous Drugs: Relationship with Glass-Forming Ability and Physicochemical Properties

Pharmaceutics ◽

10.3390/pharmaceutics11090425 ◽

2019 ◽

Vol 11 (9) ◽

pp. 425 ◽

Cited By ~ 4

Author(s):

Edueng ◽

Bergström ◽

Gråsjö ◽

Mahlin

Keyword(s):

Glass Transition ◽

Transition Temperature ◽

Glass Transition Temperature ◽

Physicochemical Properties ◽

Physical Stability ◽

Glass Forming Ability ◽

Melt Quenching ◽

Glass Forming ◽

Spray Dried

This study shows the importance of the chosen method for assessing the glass-forming ability (GFA) and glass stability (GS) of a drug compound. Traditionally, GFA and GS are established using in situ melt-quenching in a differential scanning calorimeter. In this study, we included 26 structurally diverse glass-forming drugs (i) to compare the GFA class when the model drugs were produced by spray-drying with that when melt-quenching was used, (ii) to investigate the long-term physical stability of the resulting amorphous solids, and (iii) to investigate the relationship between physicochemical properties and the GFA of spray-dried solids and their long-term physical stability. The spray-dried solids were exposed to dry (<5% RH) and humid (75% RH) conditions for six months at 25 °C. The crystallization of the spray-dried solids under these conditions was monitored using a combination of solid-state characterization techniques including differential scanning calorimetry, Raman spectroscopy, and powder X-ray diffraction. The GFA/GS class assignment for 85% of the model compounds was method-dependent, with significant differences between spray-drying and melt-quenching methods. The long-term physical stability under dry condition of the compounds was predictable from GFA/GS classification and glass transition and crystallization temperatures. However, the stability upon storage at 75% RH could not be predicted from the same data. There was no strong correlation between the physicochemical properties explored and the GFA class or long-term physical stability. However, there was a slight tendency for compounds with a relatively larger molecular weight, higher glass transition temperature, higher crystallization temperature, higher melting point and higher reduced glass transition temperature to have better GFA and better physical stability. In contrast, a high heat of fusion and entropy of fusion seemed to have a negative impact on the GFA and physical stability of our dataset.

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