ORCID Profile
0000-0002-1900-2271
Current Organisation
Argonne National Laboratory
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Publisher: Elsevier BV
Date: 04-2014
Publisher: Wiley
Date: 11-10-2021
DOI: 10.1111/JACE.18150
Abstract: Geopolymers, as a potentially environmentally friendly alternative to Portland cement, are increasingly attracting attention in the construction industry. Various methods have been applied for customizing the properties of geopolymers and improving their commercial viability. One of the promising methods for refining the properties of geopolymers such as their toughness is the use of short fibers. The effectiveness of a high‐strength short fiber in the geopolymer matrix is largely dependent on the interfacial bonding between the fiber and its surrounding matrix. While the importance of this interfacial chemistry is highlighted in the literature, the characteristics of this bonding structure have not been fully understood. In this paper, we aim to investigate the bonding mechanism between the carbon fiber and metakaolin‐based geopolymer matrix. For the first time, the existence and nature of the chemical bonding at the interfacial region (interphase) between carbon fiber and geopolymer matrix has been revealed. X‐ray pair distribution function computed tomography (PDF‐CT), field emission‐scanning electron microscopy imaging, and nanoindentation techniques are employed to discern the chemo‐mechanical properties of the interphase. PDF‐CT results show the emergence of a new atom–atom correlation at the interfacial region (around 1.82 Å). This correlation is a characteristic of interfacial bonding between the fiber and its surrounding matrix, where the existence of chemical linkages (potentially V Al‐O‐C) between fibers and the matrix contributes to the adhesion between the two constituents making up the composite. Due to such chemical bonding, the nanomechanical properties of the interfacial region fall between that of the carbon fiber and geopolymer. The combination of advanced techniques is proved useful for enhancing our understanding of the interfacial chemistry between fibers and the binding matrix. This level of knowledge facilitates the engineering of composite systems through the manipulation of their nanostructure.
Publisher: Trans Tech Publications, Ltd.
Date: 06-2011
DOI: 10.4028/WWW.SCIENTIFIC.NET/SSP.172-174.741
Abstract: In this work we compare and contrast the stability of retained austenite during tensile testing of Nb-Mo-Al transformation-induced plasticity steel subjected to different thermomechanical processing schedules. The obtained microstructures were characterised using optical metallography, transmission electron microscopy and X-ray diffraction. The transformation of retained austenite to martensite under tensile loading was observed by in-situ high energy X-ray diffraction at 1ID / APS. It has been shown that the variations in the microstructure of the steel, such as volume fractions of present phases, their morphology and dimensions, play a critical role in the strain-induced transition of retained austenite to martensite.
Publisher: Elsevier BV
Date: 2022
Publisher: Wiley
Date: 05-02-2007
Publisher: International Union of Crystallography (IUCr)
Date: 25-04-2003
DOI: 10.1107/S0909049503004643
Abstract: This paper reports on experiments in which high-energy (65.35 keV) X-rays were used to record the detailed diffuse diffraction patterns of a number of ceramic materials. The methodology has enabled a greater q-range to be explored (up to sintheta/lambda approximately 0.97) than is possible with laboratory-based experiments, with better q-space resolution and increased sensitivity, thus allowing previously unseen detail in diffraction patterns to be recorded. In all, 11 sections of data have been collected for Ca-CSZ, eight for Y-CSZ and six for wüstite.
Publisher: Wiley
Date: 08-2009
Publisher: Elsevier BV
Date: 2013
Publisher: Wiley
Date: 30-10-2009
Abstract: Boehmite (AlOOH) nanoparticles have been synthesized in subcritical (300 bar, 350 degrees C) and supercritical (300 bar, 400 degrees C) water. The formation and growth of AlOOH nanoparticles were studied in situ by small- and wide-angle X-ray scattering (SAXS and WAXS) using 80 keV synchrotron radiation. The SAXS/WAXS data were measured simultaneously with a time resolution greater than 10 s and revealed the initial nucleation of amorphous particles takes place within 10 s with subsequent crystallization after 30 s. No diffraction signals were observed from Al(OH)(3) within the time resolution of the experiment, which shows that the dehydration step of the reaction is fast and the hydrolysis step rate-determining. The sizes of the crystalline particles were determined as a function of time. The overall size evolution patterns are similar in sub- and supercritical water, but the growth is faster and the final particle size larger under supercritical conditions. After approximately 5 min, the rate of particle growth decreases in both sub- and supercritical water. Heating of the boehmite nanoparticle suspension allowed an in situ X-ray investigation of the phase transformation of boehmite to aluminium oxide. Under the wet conditions used in this work, the transition starts at 530 degrees C and gives a two-phase product of hydrated and non-hydrated aluminium oxide.
Publisher: Wiley
Date: 17-03-2011
No related grants have been discovered for Jonathan Almer.