scholarly journals On Long-Term Stability of Metallic Glasses

Metals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1076 ◽  
Author(s):  
Louzguine-Luzgin ◽  
Jiang

Thermal stability of different types of metallic glasses and partially crystalline alloys stored for at least 15 years at ambient conditions was tested in the present work by differential scanning calorimetry in comparison with that of the original alloys tested in the as-cast state in the earlier works. The structure of the naturally aged alloys was also studied by X-ray diffractometry. The structure of a couple of selected alloys was also tested by transmission electron microscopy. Most of the alloys retained their initial structure and showed only a moderate decrease in the crystallization temperature. Only those alloys which showed visible surface oxidation (Cu-Zr-system based) were partly transformed into a crystalline state forming micron-scale Cu particles in air at ambient conditions.

2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Nam-Kwang Cho ◽  
Hyun-Jae Na ◽  
Jeeyoung Yoo ◽  
Youn Sang Kim

AbstractBlack-colored (α, γ-phase) CsPbI3 perovskites have a small bandgap and excellent absorption properties in the visible light regime, making them attractive for solar cells. However, their long-term stability in ambient conditions is limited. Here, we demonstrate a strategy to improve structural and electrical long-term stability in γ-CsPbI3 by the use of an ultraviolet-curable polyethylene glycol dimethacrylate (PEGDMA) polymer network. Oxygen lone pair electrons from the PEGDMA are found to capture Cs+ and Pb2+ cations, improving crystal growth of γ-CsPbI3 around PEGDMA. In addition, the PEGDMA polymer network strongly contributes to maintaining the black phase of γ-CsPbI3 for more than 35 days in air, and an optimized perovskite film retained ~90% of its initial electrical properties under red, green, and blue light irradiation.


2021 ◽  
Vol 900 (1) ◽  
pp. 012042
Author(s):  
N Stevulova ◽  
A Estokova

Abstract This paper is addressed to comparative study of changes in thermal stability of surface-modified hemp-hurds aggregates long-term incorporated in bio-aggregate-based composites with the original ones before their integration into alternative binder matrix. In this study, the effectiveness of alkaline treatment of hemp hurds compared to the raw bio-aggregates as well as in relation to their behaviour when they are long-term incorporated in the MgO-cement environment is investigated. The differences in the thermal behaviour of the samples are explained by the changed structure of hemp hurds constituents due to the pre-treatment and long-term action of the alternative binder components on the bio-aggregates. Alkaline treatment increases thermal stability of hemp hurds compared to raw sample. Also long-term incorporation of hemp hurds in MgO-cement matrix had a similar effect in case of alkaline modified bio-aggregates. The more alkali ions present in the structure of hemp hurdssamples, the more ash is formed during their thermal decomposition studied by thermal gravimetry (TG) and differential scanning calorimetry (DSC).


2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Fujun Liu ◽  
Sophie Laurent ◽  
Alain Roch ◽  
Luce Vander Elst ◽  
Robert N. Muller

Cobalt ferrite nanoparticles (CoFe2O4NPs) were synthesized by coprecipitation followed by treatments with diluted nitric acid and sodium citrate. Transmission electron microscope (TEM) and photon correlation spectroscopy (PCS) characterization showed that the size distributions of these nanoparticles were monodisperse and that no aggregation occurred. This colloid showed a long-term stability. Through adjustment of the concentrations of reactants and reaction temperature, the size of the NPs can be tuned from 6 to 80 nm. The size-control mechanism is explained by a nucleation-growth model, where the local concentration of monomers is assumed to decide the size of nuclei, and reaction temperatures influence the growth of nuclei. Magnetization and relaxivityr1,2measurements showed that the NPs revealed size-dependent magnetization and relaxivity properties, which are explained via a “dead magnetic layer” theory where reductions of saturation magnetization (Ms) andr1,2are assumed to be caused by the demagnetization of surface spins.


2020 ◽  
pp. jclinpath-2020-206738
Author(s):  
Karin A Skalina ◽  
D Y Goldstein ◽  
Jaffar Sulail ◽  
Eunkyu Hahm ◽  
Momka Narlieva ◽  
...  

With the global outbreak of COVID-19, the demand for testing rapidly increased and quickly exceeded the testing capacities of many laboratories. Clinical tests which receive CE (Conformité Européenne) and Food and Drug Administration (FDA) authorisations cannot always be tested thoroughly in a real-world environment. Here we demonstrate the long-term stability of nasopharyngeal swab specimens for SARS-CoV-2 molecular testing across three assays recently approved by the US FDA under Emergency Use Authorization. This study demonstrates that nasopharyngeal swab specimens can be stored under refrigeration or even ambient conditions for 21 days without clinically impacting the results of the real-time reverse transcriptase-PCR testing.


NANO ◽  
2019 ◽  
Vol 14 (11) ◽  
pp. 1950138 ◽  
Author(s):  
Sai Zhang ◽  
Shijun Yue ◽  
Jiajia Li ◽  
Jianbin Zheng ◽  
Guojie Gao

Au nanoparticles anchored on core–shell [Formula: see text]-Fe2O3@SnO2 nanospindles were successfully constructed through hydrothermal synthesis process and used for fabricating a novel nonenzymatic dopamine (DA) sensor. The structure and morphology of the Au/[Formula: see text]-Fe2O3@SnO2 trilaminar nanohybrid film were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The electrochemical properties of the sensor were investigated by cyclic voltammetry and amperometry. The experimental results suggest that the composites have excellent catalytic property toward DA with a wide linear range from 0.5[Formula: see text][Formula: see text]M to 0.47[Formula: see text]mM, a low detection limit of 0.17[Formula: see text][Formula: see text]M (S/[Formula: see text]) and high sensitivity of 397.1[Formula: see text][Formula: see text]A[Formula: see text]mM[Formula: see text][Formula: see text]cm[Formula: see text]. In addition, the sensor exhibits long-term stability, good reproducibility and anti-interference.


2018 ◽  
Vol 32 (8) ◽  
pp. 1078-1091 ◽  
Author(s):  
Sibel Erol Dağ ◽  
Pınar Acar Bozkurt ◽  
Fatma Eroğlu ◽  
Meltem Çelik

A series of polystyrene (PS)/unmodified Na-montmorillonite (Na-MMT) composites were prepared via in situ radical polymerization. The prepared composites were characterized using various techniques. The presence of various functional groups in the unmodified Na-MMT and PS/unmodified Na-MMT composite was confirmed by Fourier transform infrared spectroscopy. Morphology and particle size of prepared composites was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). According to the XRD and TEM results, the interlayer spacing of MMT layers was expanded. SEM images showed a spongy and porous-shaped morphology of composites. TEM revealed the Na-MMT intercalated in PS matrix. The thermal stability of PS/unmodified Na-MMT composites was significantly improved as compared to PS, which is confirmed using thermogravimetric analysis (TGA). The TGA curves indicated that the decomposition temperature of composites is higher at 24–51°C depending on the composition of the mixture than that of pure PS. The differential scanning calorimetry (DSC) results showed that the glass transition temperature of composites was higher as compared to PS. The moisture retention, water uptake, Brunauer–Emmett–Teller specific surface area, and specific pore volume of composites were also investigated. Water resistance of the composites can be greatly improved.


2019 ◽  
Vol 56 ◽  
pp. 49-62 ◽  
Author(s):  
Javier Eliel Morales-Mendoza ◽  
Francisco Paraguay-Delgado ◽  
J.A. Duarte Moller ◽  
Guillermo Herrera-Pérez ◽  
Nicolaza Pariona

Zinc oxide (ZnO) and Zinc peroxide (ZnO2) nanoparticles were synthesized by colloidal method at low temperature. The thermal stability of ZnO2was studied by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and X-Ray diffraction (XRD). The crystalline structure and phase change from ZnO2to ZnO by heat treatment was studied in detail. Morphology and particle size was examined using Transmission Electron Microscopy (TEM), for as synthesized ZnO and ZnO2the shape of particles were cuasi-spherical for both materials with average size of 10±2.2 nm and 2.5±0.4 nm, respectively; The crystal size for ZnO obtained by heat treatment was 8±2.2 nm. Electron density contours show the chemical bond type ionic and covalent for ZnO and ZnO2. The vibrational properties were analyzed by Raman and IR spectroscopy. Band gap values were obtained from ultraviolet-visible (UV-Vis) absorbance spectrum. Photoluminescence (PL) spectrum for ZnO shows two emission edges located at 445 and 492 nm and in the case of ZnO2presents one edge at 364 nm originated from the band edge emission. The optical spectra present a hypsochromic shift, compared with some reported in the literature.


2012 ◽  
Vol 490-495 ◽  
pp. 3868-3873 ◽  
Author(s):  
Xiao Hong Yang ◽  
Xi Peng Nie ◽  
Jian Zhong Jiang

Bulk metallic glasses (BMGs) of Cu45Zr48-xAl7Tix with x= 0, 1.5, and 3 at.% were prepared by copper mould casting. The corrosion resistance of the BMGs with different Ti contents was examined by potentiodynamic polarization tests and weight loss measurements in 1 N NaOH, 1 N H2SO4, 1 N H2SO4 + 0.01 N NaCl and 0.5 N NaCl solutions, respectively. The newly-developed BMGs’ corrosion resistance in Cl-- or both H+ and Cl--ions containing solutions can be greatly enhanced. The influence of Ti addition on glass forming ability (GFA) and thermal stability was investigated by x-ray diffraction and differential scanning calorimetry in detail. The alloy containing 1.5 at.% Ti exhibits the largest GFA, the critical size comes up to 10 mm in diameter.


1998 ◽  
Vol 510 ◽  
Author(s):  
Jing xi Sun ◽  
F. J. Himpsel ◽  
T. F. Kuech

AbstractSelenium disulfide surface treatment can unpin the surface Fermi-level on n-GaAs (100) surfaces, resulting in a reduction in the surface band bending. The long-term stability of the surface Fermi-level unpinning has been studied using photoreflectance spectroscopy under room ambient conditions. Our results show that the SeS2-treated n-GaAs (100) surface is stable up to four months with negligible shift in the surface Fermi-level being noted. The mechanism of the long-term stability is attributed to the layered surface structure formed on the SeS2-treated n- GaAs (100) surface. The chemical structure of the passivated surface was determined by synchrotron radiation photoemission spectroscopy. The outermost layer of sulfur and arsenicbased sulfides and selenides may protect the electronic passivating layer, which consists of gallium-based selenides, from interaction with the atmosphere.


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