A large anisotropic plasticity of L-leucinium hydrogen maleate preserved at cryogenic temperatures

Author(s):  
S. G. Arkhipov ◽  
E. A. Losev ◽  
T. T. Nguyen ◽  
D. A. Rychkov ◽  
E. V. Boldyreva

L-Leucinium hydrogen maleate crystals are very plastic at ambient conditions. Here it is shown that this plasticity is preserved at least down to 77 K. The structural changes in the temperature range 293–100 K were followed in order to rationalize the large anisotropic plasticity in this compound. To the best of our knowledge, this is the first reported example of an organic compound remaining so plastic at cryogenic conditions.

Author(s):  
P. Moine ◽  
G. M. Michal ◽  
R. Sinclair

Premartensitic effects in near equiatomic TiNi have been pointed out by several authors(1-5). These include anomalous contrast in electron microscopy images (mottling, striations, etc. ),diffraction effects(diffuse streaks, extra reflections, etc.), a resistivity peak above Ms (temperature at which a perceptible amount of martensite is formed without applied stress). However the structural changes occuring in this temperature range are not well understood. The purpose of this study is to clarify these phenomena.


Sensors ◽  
2021 ◽  
Vol 21 (14) ◽  
pp. 4919
Author(s):  
Marcin Lebioda ◽  
Ryszard Pawlak ◽  
Jacek Rymaszewski

Microjoining technologies are crucial for producing reliable electrical connections in modern microelectronic and optoelectronic devices, as well as for the assembly of electronic circuits, sensors, and batteries. However, the production of miniature sensors presents particular difficulties, due to their non-standard designs, unique functionality and applications in various environments. One of the main challenges relates to the fact that common methods such as reflow soldering or wave soldering cannot be applied to making joints to the materials used for the sensing layers (oxides, polymers, graphene, metallic layers) or to the thin metallic layers that act as contact pads. This problem applies especially to sensors designed to work at cryogenic temperatures. In this paper, we demonstrate a new method for the dynamic soldering of outer leads in the form of metallic strips made from thin metallic layers on ceramic substrates. These leads can be used as contact pads in sensors working in a wide temperature range. The joints produced using our method show excellent electrical, thermal, and mechanical properties in the temperature range of 15–300 K.


2021 ◽  
Vol 8 (4) ◽  
pp. 20218411
Author(s):  
N. A. Zhestkij ◽  
E. V. Gunina ◽  
S. P. Fisenko ◽  
A. E. Rubtsov ◽  
D. A. Shipilovskikh ◽  
...  

The synthesis of (E)-2-((3-(ethoxycarbonyl)-5-methyl-4-phenylthiophen-2-yl)amino)-4-oxo-4-(p-tolyl)but-2-enoic acid was performed. This organic compound was used as a building block for the organic molecular crystals with highly stable photoluminescence at ambient conditions, which has been established during 10 years of exploitation.


2003 ◽  
Vol 771 ◽  
Author(s):  
G. Heimel ◽  
P. Puschnig ◽  
M. Oehzelt ◽  
K. Hummer ◽  
B. Koppelhuber-Bitschnau ◽  
...  

AbstractIn this work, we report on pressure induced structural changes in crystalline oligo(paraphenylenes) containing two to six phenyl rings. Revisiting the crystal structures at ambient conditions reveals details in the packing principle. A linear relationship between the density at ambient conditions and the number of phenyl rings is found. Energy dispersive X-ray diffraction has been performed in a systematic study on polycrystalline powders of biphenyl, paraterphenyl, p-quaterphenyl, p-quinquephenyl and p-sexiphenyl under hydrostatic pressure up to 60 kbar. Our investigations not only yield pressure dependent lattice parameters and hints towards pressure induced changes in the molecular arrangement, but also allow for an analysis of the equations of state of these substances as a function of oligomer length. We report the previously unknown bulk modulus of p-quaterphenyl, p-quinquephenyl, and p-sexiphenyl (B0 = 83 kbar, 93 kbar, and 100 kbar respectively) and its pressure derivative (B0' = 6.4, 7.5, and 5.6). A linear dependence of the bulk modulus on the inverse number of phenyl rings in the molecules is found.


1985 ◽  
Vol 59 ◽  
Author(s):  
L. A. Ladd ◽  
J. P. Kalejs

ABSTRACTCarbon diffusivity is reported for different ambient conditions imposed during annealing of silicon in the temperature range from 800 to 100°C, which produce varying levels of silicon self-interstitial supersaturation. The diffusivities are deduced from SIMS analysis of carbon out-diffusion profiles. Carbon diffusivity is increased by up to a factor of 70 in annealing with phosphorus in-diffusion, and by a factor of as much as seven in an oxidizing ambient, when compared to anneals in a nitrogen ambient. The enhancements tend to decrease above 11000C. This behavior can be explained by attributing the increase in carbon diffusivity to self-interstitial supersaturation which increases the concentration of highly mobile carbon selfinterstitial pairs. Significant time dependent effects were also observed for 800 and 9000C phosphorus in-diffusion conditions.


2014 ◽  
Vol 1040 ◽  
pp. 303-308 ◽  
Author(s):  
Andrey Klishin ◽  
Alexander Kovancev ◽  
Stanislav Rudnev ◽  
Alexander Zakutaev ◽  
Vladimir Vereshchagin

The issues of structural changes produced in ceramic materials on the basis of Al2O3and ZrO2(Y2O3) during thermomagnetic processing (B=0.02–1 T) are considered. The contribution of the electromagnetic field to the linear shrinkage of processed ceramic samples has been estimated to be 1–6%. The possibility of using the thermomagnetic processing method for obtaining the disperse and homogeneous structure has been shown. The technological modes of processing under the electromagnetic field are suggested, facilitating self-cleaning and perfecting the crystalline structures of Al2O3and ZrO2(Y2O3), including annealing in the temperature range of 800–1200 °C within 8–12 hours.


2009 ◽  
Vol 131 (7) ◽  
Author(s):  
Eduardo Reátegui ◽  
Alptekin Aksan

Proteins and enzymes can be encapsulated in nanoporous gels to develop novel technologies for biosensing, biocatalysis, and biosynthesis. When encapsulated, certain macromolecules retain high levels of activity and functionality and are more resistant to denaturation when exposed to extremes of pH and temperature. We have utilized intrinsic fluorescence and Fourier transform infrared spectroscopy to determine the structural transitions of encapsulated lysozyme in the range of −120°C<T<100°C. At cryogenic temperatures encapsulated lysozyme did not show cold denaturation, instead became more structured. However, at high temperatures, the onset of heat denaturation of confined lysozyme was reduced by 15°C when compared with lysozyme in solution. Altered dynamics of the solvent and pore size distribution of the nanopores in the matrix appear to be key factors influencing the decrease in the denaturation temperature.


2009 ◽  
Vol 65 (6) ◽  
pp. 770-781 ◽  
Author(s):  
Tatiana N. Drebushchak ◽  
Yury A. Chesalov ◽  
Elena V. Boldyreva

Structural changes in the high-temperature ∊-polymorph of chlorpropamide, 4-chloro-N-(propylaminocarbonyl)benzenesulfonamide, C10H13ClN2O3S, on cooling down to 100 K and on reverse heating were followed by single-crystal X-ray diffraction. At temperatures below 200 K the phase transition into a new polymorph (termed the ∊′-form) has been observed for the first time. The polymorphic transition preserves the space group Pna21, is reversible and is accompanied by discontinuous changes in the cell volume and parameters, resulting from changes in molecular conformation. As shown by IR spectroscopy and X-ray powder diffraction, the phase transition in a powder sample is inhomogeneous throughout the bulk, and the two phases co-exist in a wide temperature range. The cell parameters and the molecular conformation in the new polymorph are close to those in the previously known α-polymorph, but the packing of the z-shaped molecular ribbons linked by hydrogen bonds inherits that of the ∊-form and is different from the packing in the α-polymorph. A structural study of the α-polymorph in the same temperature range has revealed no phase transitions.


1989 ◽  
Vol 67 (7) ◽  
pp. 686-693 ◽  
Author(s):  
S. O. Kasap ◽  
S. Yannacopoulos

Mechanical and thermal properties of a typical X-ray imaging material amorphous Se0.997As0.003, chlorinated in the ppm range were investigated using thermal microhardness analysis (TμHA) and differential scanning calorimetry (DSC). The experiments were carried out over a temperature range encompassing the glass transformation to study the nature of structural changes controlling the mechanical and thermal properties. It is shown that the mechanical property microhardness when examined on an Itoh–Shishokin plot of log Vickers hardness number (VHN) vs. temperature (T) exhibits a hardness transition temperature, Tg*, in the glass transformation region. The rates of relaxation of the mechanical and thermal properties in the glass transformation region were studied by investigating the heating rate dependence of the glass transition temperatures, Tg* and Tg, defined empirically on the log VHN vs. T behavior and the DSC glass transformation endotherm, respectively. By applying the present thermoanalytical methods, it has proved possible to identify a typical Vogel–Tammann–Fulcher type of behavior in the mechanical and thermal relaxation times that correlates remarkably well with the viscosity–temperature data of M. Cukierman and D. R. Uhlmann (J. Non-Cryst. Solids, 12, 199 (1973)) as well as the dielectric loss experiments of M. Abkowitz, D. F. Pochan, and J. M. Pochan (J. Appl. Phys. 51, 1539 (1980)). The latter had previously exposed a Williams–Landel–Ferry relation for the Debye relaxation times in a-Se and a-Se: 1% As. It is therefore concluded that the behavior of mechanical, thermal, and dielectric properties of a-Se0997As0003 in the glass transformation region is inversely proportional to the viscosity, which in turn can be adequately described over a temperature range above ~30 °C by a Vogel expression.


2000 ◽  
Vol 623 ◽  
Author(s):  
D.P. Eakin ◽  
M.G. Norton ◽  
D.F. Bahr

AbstractThin films of PZT were deposited onto platinized and bare single crystal NaCl using spin coating and sol-gel precursors. These films were then analyzed using in situ heating in a transmission electron microscope. The results of in situ heating are compared with those of an ex situ heat treatment in a standard furnace, mimicking the heat treatment given to entire wafers of these materials for use in MEMS and ferroelectric applications. Films are shown to transform from amorphous to nanocrystalline over the course of days when held at room temperature. While chemical variations are found between films crystallized in ambient conditions and films crystallized in the vacuum conditions of the microscope, the resulting crystal structures appear to be insensitive to these differences. Significant changes in crystal structure are found at 500°C, primarily the change from largely amorphous to the beginnings of clearly crystalline films. Crystallization does occur over the course of weeks at room temperature in these films. Structural changes are more modest in these films when heated in the TEM then those observed on actual wafers. The presence of Pt significantly influences both the resulting structure and morphology in both in situ and ex situ heated films. Without Pt present, the films appear to form small, 10 nm grains consisting of both cubic and tetragonal phases, whereas in the case of the Pt larger, 100 nm grains of a tetragonal phase are formed.


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