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    Stress Corrosion Cracking in APS-Glasses

    Subjects: Others
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    Submitted by: Houizot Patrick

    Definition

    Stress corrosion cracking is a well-known phenomenon in oxide glasses. However, how amorphous phase separation (APS) alters stress corrosion cracking, and the overall mechanical response of an oxide glass is less known in literature. APS is a dominant feature concerning many multicomponent systems, particularly the ternary sodium borosilicate (SBN) glass systems.

    1. Introduction

    Since Before the Common Era, humankind has been fabricating oxide glasses for various uses. Over the years, interest in oxide glasses has grown due to advantageous optical, chemical, and electrical properties [1]. Some of these properties include optical transparency, electrical isolation, and a high melting point (between 800–1800 °C depending on the chemical composition). Yet oxide glasses have a major drawback: they seem to fail abruptly. However, studying the failure of the glass samples in detail frequently leads one to discover sub-critical crack growth, also called stress corrosion cracking (SCC) because it is aided by environmental factors, or flaws that occurred before the dynamic fracture. For homogenous oxide glasses, this phenomenon is well documented in literature [2][3][4][5][6][7][8][9][10][11]. Moreover, the SCC properties are known to depend on the chemical composition of the oxide glass [2][3][4], the fictive temperature [5][6], the environmental factors [7][8][9][10][11], etc. In recent years, it has become apparent that understanding dynamic and sub-critical cracking requires a detailed knowledge of how short- and medium-range structures influence physical and mechanical properties in these glasses. By gaining this deep understanding, researchers will obtain key knowledge to advancing glass technology. This will ultimately benefit all kinds of industry, including high technology fields such as laser technology, energy-saving technology, and communication technology.

    A single-phase material has a structurally and chemically homogeneous distribution of its constituents. Multiphase materials occur when precipitates with structural and/or chemical composition differences form. Each phase in these materials is homogeneous, and there is a distinctive barrier between different phases [12][13][14]. Liquid–liquid phase separation occurs in multi-component liquids when the Gibbs energy curve shows two distinct minimums as a function of the liquid composition.

    From a thermodynamic viewpoint, a simple binary system composed of components A and B can exist as a homogenous mixture (attractive interactions A–B), or it might prefer to exist as a heterogeneous mixture with repulsive A–B interactions. The preference to exist as a heterogeneous mixture induces phase separation over a well-defined range of compositions, temperatures, and pressures. Likewise, phase separation can also be due to irradiation [15]. Phase separation processes produce a large variety of mesoscopic structures, which modify the macroscopic behavior of the material. Theories propose different mechanisms to explain these scenarios taking into consideration the composition of the glass and the kinetic limits [16][17].

    Over the years, researchers identified metastable miscibility gaps in multiple different types of oxide glass systems [18][19][20], particularly those based on silica and boron oxides [21][22][23]. Simulation and experimental approaches aid in obtaining phase diagrams to predict the miscibility gaps. These studies [24][25][26][27][28][29] help in understanding from short- to medium-range (micro and meso) structures of the glasses. Researchers also study how these changes scale up to variations in the overall physical and mechanical/fracture properties of phase separated glass systems [30][31]. An industrial application of phase separated glasses and their enhanced mechanical/fracture properties concerns crush-resistant glasses [32]. Furthermore, phase diagrams have industrial significance when considering functional materials, such as glass-ceramics and porous glasses [33][34][35].

    2. Thermodynamic Interpretations of Phase Separation

    Thermodynamic theories are some of the most widely accepted methods for explaining the occurrence of phase separation in materials. Section 3.1 reviews the case of a two-atom theoretical system. Section 3.2 turns to the more complex problem of multi-oxide glass systems. Section 3.3 addresses the special case of SiO 2- B 2O 3- Na 2O glasses. APS in glasses is usually considered and analyzed as liquid–liquid phase separation [17][36][37]. However, it should be noted that a glass is not in thermodynamic equilibrium; hence, discussions herein concern inherently metastable glasses.

    Figure 1 depicts a typical miscibility gap and the Gibbs free energy curves as a function of x B . In Figure 1 a, the solid dark blue line represents the binodal curve, which is the boundary between the domain where only a single phase exists to a domain where multiple phases exist, and hence a miscibility gap. This curve is obtained from the shape variation of Gibbs free energy curves ( Figure 1 b,c).

    Figure 3. (a) Schematic two-liquid immiscibility region showing binodal (zone I) and spinodal (zone II); (b) Sketch of the Gibbs free energy curve versus composition Xb (mole fraction of component B) for temperature T1 where T1 > Tc and (c) Gibbs free energy curve versus composition xB (mole fraction of component B) for temperature T2 < Tc. Binodal decomposition occurs in zone I, and spinodal decomposition occurs in zone II [17][38][39]

    For many years, the CALPHAD (CALculation of PHAse Diagrams) method was used to provide predictions of liquid phase miscibility gaps in multiple different systems [40][41]. This method uses the Gibbs energy to calculate phase diagrams and thermodynamic properties. Input parameters include conditions such as chemical composition, temperature, and pressure. Extending CALPHAD methods to oxide glasses may give reliable estimates of the phase diagram [42], yet this is proving difficult because glass is not at equilibrium.

    Generally, the ternary metastable liquid–liquid phase diagram is highly important. Moreover, kinetic factors also have essential effects on the phase separation processes. For a given glass with a chemical composition within the miscibility gap, annealing protocols determine: (1) the phase composition while attaining equilibrium ( Section 3.1 ), (2) the type of phase separation (binodal or spinodal) [43], (3) the nucleation/growth kinetics in the miscibility gaps [37][44], and (4) the final phase compositions and phase size [45][46][47]. The next section focuses on different structures of some APS-SBN (amorphous phase separated SBN) glasses.

    3. Physical Properties of APS Glasses

    The inherent structure of the glass and its amorphous phase separated counterpart could play a role in altering physical and mechanical/fracture glass properties. In this section, we take a closer look at how the APS structure of the glasses plays on the physical properties where Section 6 concentrates on the mechanical/fracture properties.

    APS produces a large variety of structures in glasses. This affects the density calculations. Burnett and Douglas’ [37] investigations found that phase separation consists of two distinctive stages: (i) the decomposition stage when the developing phases gradually reaches the equilibrium composition; and (ii) the coarsening stage when the size of the phase separation regions increases without considerable changes in phase composition. At the end of the first stage, the dimension of phase separated regions are usually large enough to neglect the interfacial effects between different phases [48]. In this case, a two-phase glass can be considered as a composite material consisting of two different homogeneous substances, i.e., the tie-line end members .

    From the above equations, the sign of the first derivative does not change with w B , and it depends on the quantitative comparison between ρ α and ρ β . Additionally, the second derivative is always positive. This shows that the curve of ρ as a function of one component’s initial weight fraction is convex.

    The comparison between experiments and theory shows the wide usability of Equations (16) and (17). This analysis is also valid for ternary and higher-order systems in a two-phase region. In these regions, the above equations are valid if one follows the tie line of constant temperature [49][50].

    4. Mechanical/Fracture Properties of APS Glasses

    Glass is one of the most common materials in daily life due to many advantageous properties, including transparency, thermal and chemical stability, etc. However, its biggest disadvantage is its brittleness, which limits its uses in many applications. This is still the case despite a long history of developments aiming at overcoming this drawback [51][52][53][54]. To understand the mechanical/fracture properties of APS glasses, Section 6.1 first takes a closer look at the Young’s modulus of APS glasses. It highlights the PbO - B 2O 3 glass systems discussed in Section 5 . Then, Section 6.2 addresses some fracture properties of APS glasses, including the interaction between the crack front and secondary phases during dynamic fracture ( Section 6.2.1 ), fracture toughness ( Section 6.2.2 ), sub-critical cracking ( Section 6.2.3 ) and post-mortem fracture surface analysis ( Section 6.2.4 ).

    Likewise, Miyata et al. [55] studied B 2O 3-rich particles in a PbO -rich matrix (i.e., α m < α p , Γ m < Γ p , and E m > E p ). With all the theoretical analysis above, they proposed that the crack passes around the particles in this system.

    As stated above, APS in glasses alters crack propagation at the mesoscale. Hence, macroscopic fracture properties should be influenced by these medium-range structural variations [56]. It has been widely considered that the presence of APS systematically increases the fracture toughness of the glass [57][58]. Several toughening mechanisms have been proposed to explain how heterogeneous inclusions affect the fracture behavior as it is mentioned at the beginning of Section 6.2.1 (crack pinning, deflection, trapping, etc.).

    As was analyzed in Section 6.2.1 [55], for the PbO -rich particles/ B 2O 3-rich matrix where α m > α p , Γ m > Γ p , and E m < E p , the crack propagates preferentially through the PbO -rich phase; for the B 2O 3-rich particles/ PbO -rich matrix where α m < α p , Γ m < Γ p , and E m > E p , the crack propagates preferentially around the B 2O 3-rich “impenetrable” particles.

    The entry is from 10.3390/cmd2030022

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