scholarly journals Toward a Better Understanding of Activation Volume and Dynamic Decoupling of Glass‐Forming Liquids under Compression

2021 ◽  
pp. 2100035
Author(s):  
Anh D. Phan ◽  
Nguyen K. Ngan ◽  
Nam B. Le ◽  
Le T. M. Thanh
2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Aleksandra Drozd-Rzoska

Abstract In pressurized glass-forming systems, the apparent (changeable) activation volume Va(P) is the key property governing the previtreous behavior of the structural relaxation time (τ) or viscosity (η), following the Super-Barus behavior: $${\boldsymbol{\tau }}{\boldsymbol{(}}{\boldsymbol{P}}{\boldsymbol{)}}{\boldsymbol{,}}{\boldsymbol{\eta }}{\boldsymbol{(}}{\boldsymbol{P}}{\boldsymbol{)}}{\boldsymbol{\propto }}{\bf{\exp }}{\boldsymbol{(}}{{\boldsymbol{V}}}_{{\boldsymbol{a}}}{\boldsymbol{(}}{\boldsymbol{P}}{\boldsymbol{)}}{\boldsymbol{/}}{\boldsymbol{R}}{\boldsymbol{T}}{\boldsymbol{)}}$$ τ ( P ) , η ( P ) ∝ exp ( V a ( P ) / R T ) , T = const. It is usually assumed that Va(P) = V#(P), where $${{\boldsymbol{V}}}^{{\boldsymbol{\#}}}{\boldsymbol{(}}{\boldsymbol{P}}{\boldsymbol{)}}={\boldsymbol{R}}{\boldsymbol{T}}{\boldsymbol{d}}\,{\boldsymbol{ln}}\,{\boldsymbol{\tau }}{\boldsymbol{(}}{\boldsymbol{P}}{\boldsymbol{)}}{\boldsymbol{/}}{\boldsymbol{d}}{\boldsymbol{P}}$$ V # ( P ) = R T d ln τ ( P ) / d P or $${{\boldsymbol{V}}}^{{\boldsymbol{\#}}}{\boldsymbol{(}}{\boldsymbol{P}}{\boldsymbol{)}}{\boldsymbol{=}}{\boldsymbol{R}}{\boldsymbol{T}}{\boldsymbol{d}}\,{\boldsymbol{ln}}\,{\boldsymbol{\eta }}{\boldsymbol{(}}{\boldsymbol{P}}{\boldsymbol{)}}{\boldsymbol{/}}{\boldsymbol{d}}{\boldsymbol{P}}$$ V # ( P ) = R T d ln η ( P ) / d P . This report shows that Va(P) ≪ V#(P) for P → Pg, where Pg denotes the glass pressure, and the magnitude V#(P) is coupled to the pressure steepness index (the apparent fragility). V#(P) and Va(P) coincides only for the basic Barus dynamics, where Va(P) = Va = const in the given pressure domain, or for P → 0. The simple and non-biased way of determining Va(P) and the relation for its parameterization are proposed. The derived relation resembles Murnaghan - O’Connel equation, applied in deep Earth studies. It also offers a possibility of estimating the pressure and volume at the absolute stability limit. The application of the methodology is shown for diisobutyl phthalate (DIIP, low-molecular-weight liquid), isooctyloxycyanobiphenyl (8*OCB, liquid crystal) and bisphenol A/epichlorohydrin (EPON 828, epoxy resin), respectively.


2012 ◽  
Vol 24 (6) ◽  
pp. 065105 ◽  
Author(s):  
K Kaminski ◽  
S Pawlus ◽  
K Adrjanowicz ◽  
Z Wojnarowska ◽  
P Wlodarczyk ◽  
...  

2011 ◽  
Vol 84 (5) ◽  
Author(s):  
Marian Paluch ◽  
Sebastian Pawlus ◽  
Andrzej Grzybowski ◽  
Katarzyna Grzybowska ◽  
Patryk Włodarczyk ◽  
...  

2020 ◽  
Vol 53 (17) ◽  
pp. 7239-7252 ◽  
Author(s):  
Wen-Sheng Xu ◽  
Jack F. Douglas ◽  
Wenjie Xia ◽  
Xiaolei Xu

2011 ◽  
Vol 2011 ◽  
pp. 1-10 ◽  
Author(s):  
Soheil Sharifi ◽  
Jahanbakhsh Mashaiekhy Asl

The physical properties of the glass depend on the procedure used to produce the glass. In particular, if the glass is obtained through the variation of external thermodynamic parameters, the specific way in which the parameters are varied (thermodynamic history) has influence on the final properties. In this work, we studied the effect of thermodynamic history on secondary relaxation inside the glassy state on different molecular glass forming, namely, PPGE(poly[(phenyl glycidyl ether)-co-formaldehyde]), 1,18-bis (p methoxyphenyl) cyclohexane (BMPC), poly(propylene glycol)—(PPG400), phenolphthalein-dimethyl-ether(PDE), Poly(vinyl acetate) (PVAc), and poly(bisphenol A-co-epichlorohydrin) glycidyl end-capped (DGEBA). We found secondary relaxation change with thermodynamic history and depends on the value of the activation volume which activation entropy of secondary relaxation inside the glassy state. Also, we found most of the JG secondary relaxation change with thermodynamic history and most of the Non-JG secondary relaxation are not sensitive.


Author(s):  
Gareth Thomas

Silicon nitride and silicon nitride based-ceramics are now well known for their potential as hightemperature structural materials, e.g. in engines. However, as is the case for many ceramics, in order to produce a dense product, sintering additives are utilized which allow liquid-phase sintering to occur; but upon cooling from the sintering temperature residual intergranular phases are formed which can be deleterious to high-temperature strength and oxidation resistance, especially if these phases are nonviscous glasses. Many oxide sintering additives have been utilized in processing attempts world-wide to produce dense creep resistant components using Si3N4 but the problem of controlling intergranular phases requires an understanding of the glass forming and subsequent glass-crystalline transformations that can occur at the grain boundaries.


Author(s):  
Matthew R. Libera ◽  
Martin Chen

Phase-change erasable optical storage is based on the ability to switch a micron-sized region of a thin film between the crystalline and amorphous states using a diffraction-limited laser as a heat source. A bit of information can be represented as an amorphous spot on a crystalline background, and the two states can be optically identified by their different reflectivities. In a typical multilayer thin-film structure the active (storage) layer is sandwiched between one or more dielectric layers. The dielectric layers provide physical containment and act as a heat sink. A viable phase-change medium must be able to quench to the glassy phase after melting, and this requires proper tailoring of the thermal properties of the multilayer film. The present research studies one particular multilayer structure and shows the effect of an additional aluminum layer on the glass-forming ability.


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