In-Situ Investigations of the Fracture Mechanisms at Various Length Scales

Author(s):  
Zbigniew Pakiela ◽  
Witold Zielinski ◽  
Krzysztof J. Kurzydlowski
2020 ◽  
Vol 61 (6) ◽  
Author(s):  
C E Schrank ◽  
K Gioseffi ◽  
T Blach ◽  
O Gaede ◽  
A Hawley ◽  
...  

Abstract We present a review of a unique non-destructive method for the real-time monitoring of phase transformations and nano-pore evolution in dehydrating rocks: transmission small- and wide-angle synchrotron X-ray scattering (SAXS/WAXS). It is shown how SAXS/WAXS can be applied to investigating rock samples dehydrated in a purpose-built loading cell that allows the coeval application of high temperature, axial confinement, and fluid pressure or flow to the specimen. Because synchrotron sources deliver extremely bright monochromatic X-rays across a wide energy spectrum, they enable the in situ examination of confined rock samples with thicknesses of ≤ 1 mm at a time resolution of order seconds. Hence, fast kinetics with reaction completion times of about hundreds of seconds can be tracked. With beam sizes of order tens to hundreds of micrometres, it is possible to monitor multiple interrogation points in a sample with a lateral extent of a few centimetres, thus resolving potential lateral spatial effects during dehydration and enlarging sample statistics significantly. Therefore, the SAXS/WAXS method offers the opportunity to acquire data on a striking range of length scales: for rock samples with thicknesses of ≤ 10-3 m and widths of 10-2 m, a lateral interrogation-point spacing of ≥ 10-5 m can be achieved. Within each irradiated interrogation-point volume, information concerning pores with sizes between 10-9 and 10-7 m and the crystal lattice on the scale of 10-10 m is acquired in real time. This article presents a summary of the physical principles underpinning transmission X-ray scattering with the aim of providing a guide for the design and interpretation of time-resolved SAXS/WAXS experiments. It is elucidated (1) when and how SAXS data can be used to analyse total porosity, internal surface area, and pore-size distributions in rocks on length scales from ∼1 to 300 nm; (2) how WAXS can be employed to track lattice transformations in situ; and (3) which limitations and complicating factors should be considered during experimental design, data analysis, and interpretation. To illustrate the key capabilities of the SAXS/WAXS method, we present a series of dehydration experiments on a well-studied natural gypsum rock: Volterra alabaster. Our results demonstrate that SAXS/WAXS is excellently suited for the in situ tracking of dehydration kinetics and the associated evolution of nano-pores. The phase transformation from gypsum to bassanite is correlated directly with nano-void growth on length scales between 1 and 11 nm for the first time. A comparison of the SAXS/WAXS kinetic results with literature data emphasises the need for future dehydration experiments on rock specimens because of the impact of rock fabric and the generally heterogeneous and transient nature of dehydration reactions in nature. It is anticipated that the SAXS/WAXS method combined with in situ loading cells will constitute an invaluable tool in the ongoing quest for understanding dehydration and other mineral replacement reactions in rocks quantitatively.


2018 ◽  
Vol 24 (S1) ◽  
pp. 1010-1011
Author(s):  
Will Harris ◽  
Hrishikesh Bale ◽  
Steve Kelly ◽  
Benjamin Hornberger

Materials ◽  
2020 ◽  
Vol 13 (17) ◽  
pp. 3775
Author(s):  
Chiara Bertolin ◽  
Lavinia de Ferri ◽  
Filippo Berto

The main issue of wood is its sensitivity to Relative Humidity (RH) variations, affecting its dimensional stability, and thus leading to crack formations and propagations. In situ structural health monitoring campaigns imply the use of portable noninvasive techniques such as acoustic emission, used for real-time detection of energy released when cracks form and grow. This paper proposes a calibration method, i.e., acoustic emission, as an early warning tool for estimating the length of new formed cracks. The predictability of ductile and brittle fracture mechanisms based on acoustic emission features was investigated, as well as climate-induced damage effect, leading to a strain-hardening mechanism. Tensile tests were performed on specimens submitted to a 50% RH variation and coated with chemicals to limit moisture penetration through the radial surfaces. Samples were monitored for acoustic emission using a digital camera to individuate calibration curves that correlated the total emitted energy with the crack propagation, specifically during brittle fracture mechanism, since equations provide the energy to create a new surface as the crack propagates. The dynamic surface energy value was also evaluated and used to define a Locus of Equilibrium of the energy surface rate for crack initiation and arrest, as well as to experimentally demonstrate the proven fluctuation concept.


2005 ◽  
Vol 290 ◽  
pp. 208-213 ◽  
Author(s):  
S. Bueno ◽  
Carmen Baudín

Alumina (Al2O3)-aluminium titanate (Al2TiO5) composites present higher toughness than alumina materials but rather low strength due to microcracking. Laminates in which a flaw tolerant material is located between high strength layers is one way to overcome this problem. In this work, the fracture behaviour of a laminated structure constituted by five layers, where low residual stresses are expected, is studied. In this system, external and central layers of monophase alumina with high strength were combined with intermediate layers of alumina with 10vol.% of aluminium titanate. In the monophase alumina layers, an additional "in situ" formed layer of about 200 µm, constituted by large (@10µm) grains was found, close to the composite layers. The laminated structure presented semistable behaviour during SENVB tests for conditions in which stable crack propagation is not predicted for small grain sized alumina materials. Toughening mechanisms related to thermal expansion mismatch between matrix and second phase in the composite layers and crack bridging in the large grain sized alumina layer were identified.


2018 ◽  
Vol 24 (S1) ◽  
pp. 1808-1809
Author(s):  
Rohan Dhall ◽  
Matthew Cabral ◽  
Abinash Kumar ◽  
James M. LeBeau

2018 ◽  
Vol 723 ◽  
pp. 79-88 ◽  
Author(s):  
W.P. Li ◽  
X.G. Wang ◽  
B. Liu ◽  
Q.H. Fang ◽  
C. Jiang

Nanoscale ◽  
2015 ◽  
Vol 7 (7) ◽  
pp. 3022-3027 ◽  
Author(s):  
Evgheni Strelcov ◽  
Joshua Cothren ◽  
Donovan Leonard ◽  
Albina Y. Borisevich ◽  
Andrei Kolmakov

Progress in rational engineering of Li-ion batteries requires better understanding of the electrochemical processes and accompanying transformations in the electrode materials on multiple length scales.


2017 ◽  
Vol 50 (5) ◽  
pp. 1404-1410 ◽  
Author(s):  
Roland Morak ◽  
Stephan Braxmeier ◽  
Lukas Ludescher ◽  
Florian Putz ◽  
Sebastian Busch ◽  
...  

A newin situsetup combining small-angle neutron scattering (SANS) and dilatometry was used to measure water-adsorption-induced deformation of a monolithic silica sample with hierarchical porosity. The sample exhibits a disordered framework consisting of macropores and struts containing two-dimensional hexagonally ordered cylindrical mesopores. The use of an H2O/D2O water mixture with zero scattering length density as an adsorptive allows a quantitative determination of the pore lattice strain from the shift of the corresponding diffraction peak. This radial strut deformation is compared with the simultaneously measured macroscopic length change of the sample with dilatometry, and differences between the two quantities are discussed on the basis of the deformation mechanisms effective at the different length scales. It is demonstrated that the SANS data also provide a facile way to quantitatively determine the adsorption isotherm of the material by evaluating the incoherent scattering contribution of H2O at large scattering vectors.


2021 ◽  
Vol 2076 (1) ◽  
pp. 012047
Author(s):  
Ziyan Pan ◽  
Mingduo Yuan ◽  
Zhenyu Zou ◽  
Weijian Zhang ◽  
Mingyue Du ◽  
...  

Abstract In this study, the fracture mechanisms of Cr-coated Zr4 alloy samples were studied by in-situ tensile testing with high-resolution observations. Both original sample and pre-oxidized sample were studied to study the effects of pre-oxidation on the cracking and failure behavior. For the Cr-coated Zr4 sample, with the increase of tensile strain, multiple surface cracks were dominant and less interfacial cracks were formed, indicating good interfacial strength of Cr coating. For the pre-oxidized samples, there was a thin oxide layer formed on the Cr coating surface, revealing improved oxidation resistance and protection effects. However, a brittle ZrCr2 diffusion layer was formed in the same while at the Cr/Zr4 interface underneath the Cr coating, which would lead to earlier micro-cracks formed under tensile stress and evidently degrade the interfacial strength. The findings in the study indicated the importance of optimizing coating microstructure in future study to avoid forming the above-mentioned brittle diffusion interlayer and the associated premature failure.


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