scholarly journals Design of magnetic spirals in layered perovskites: Extending the stability range far beyond room temperature

2018 ◽  
Vol 4 (10) ◽  
pp. eaau6386 ◽  
Author(s):  
Tian Shang ◽  
Emmanuel Canévet ◽  
Mickaël Morin ◽  
Denis Sheptyakov ◽  
María Teresa Fernández-Díaz ◽  
...  

In insulating materials with ordered magnetic spiral phases, ferroelectricity can emerge owing to the breaking of inversion symmetry. This property is of both fundamental and practical interest, particularly with a view to exploiting it in low-power electronic devices. Advances toward technological applications have been hindered, however, by the relatively low ordering temperatures Tspiral of most magnetic spiral phases, which rarely exceed 100 K. We have recently established that the ordering temperature of a magnetic spiral can be increased up to 310 K by the introduction of chemical disorder. Here, we explore the design space opened up by this novel mechanism by combining it with a targeted lattice control of some magnetic interactions. In Cu-Fe layered perovskites, we obtain Tspiral values close to 400 K, comfortably far from room temperature and almost 100 K higher than using chemical disorder alone. Moreover, we reveal a linear relationship between the spiral’s wave vector and the onset temperature of the spiral phase. This linear law ends at a paramagnetic-collinear-spiral triple point, which defines the highest spiral ordering temperature that can be achieved in this class of materials. On the basis of these findings, we propose a general set of rules for designing magnetic spirals in layered perovskites using external pressure, chemical substitutions, and/or epitaxial strain, which should guide future efforts to engineer magnetic spiral phases with ordering temperatures suitable for technological applications.

1928 ◽  
Vol 28 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Alexander Joe ◽  
J. C. J. McEntee

The stability of the biological reagents used in routine immunological procedures is a matter of practical interest to the public health worker, and an attempt has been made in the following research to estimate the period during which the diluted toxin used in the Schick test for the estimation of susceptibility to diphtheria remains potent. In the early days of Schick testing, although Leete (1920) reported that a diluted toxin retained its potency for as long as 5 weeks, it has hitherto been considered inadvisable to use a toxin at a longer interval than 48 hours after it had been diluted to its proper strength. Glenny, Waddington and Pope (1928) and O'Brien, Okell and Parish (1928) have introduced a new diluent consisting of a solution of a combination of crystal borax 57, boric acid 84 and sodium chloride 99 parts. A 1·5 per cent, solution of this mixture is now used as a diluent and has the effect of sustaining the potency of the diluted toxin over a greater period of time. In our work over 400 persons have been tested with toxins made up according to this formula, a comparison being made in each individual between the reactions elicited by an aged toxin, stored for varying periods at room temperature or in the cold room, with those produced by a fresh toxin. Enough toxin was made up at the beginning of the experiment to last over a considerable period of time, samples being sent to us by post periodically together with batches of freshly diluted toxin. The testing of reagents was carried out immediately on receipt, the lower age groups being selected in any series of individuals as being likely to give the largest number of reactors. The actual testing was performed practically throughout by one of us (J. C. J. McEntee) so as to maintain uniformity of technique. Each pair of toxins was controlled by a single injection of inactivated toxin and the results were scrutinised at the 4th and 10th days, a record of the comparative intensities of the positives being made at the same time. The results are recorded in Table I.


2002 ◽  
Vol 17 (5) ◽  
pp. 1129-1135 ◽  
Author(s):  
C. Métraux ◽  
B. Grobéty ◽  
P. Ulmer

Nanowires were produced by injection of molten Hg and Pb into chrysotile nanotubes. The breakdown of chrysotile and the surface tension of the molten metals are the limiting factors for the filling procedure. The thermal stability of chrysotile nanotubes was investigated by infrared spectrometry, thermogravimetry, differential thermal analysis, and x-ray diffraction analyses. For short-term thermal annealing (30 min) the tube morphology remains stable up to 700 °C. The high surface tension of both molten Pb and Hg (γLV > 200 mN/m) requires external pressure for the melts to penetrate into the tubes. Filling of the tubes was achieved under high pressure and high temperature conditions compatible with the stability range for chrysotile determined in the annealing experiments. Transmission electron microscopy observations confirmed high filling yields for both metals. Almost all nanotubes were partially filled with lead. The length of continuous wires ranged from tens to hundreds of nanometers. Additional experiments with tin were not successful.


2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Anastasiia S. Varentcova ◽  
Stephan von Malottki ◽  
Maria N. Potkina ◽  
Grzegorz Kwiatkowski ◽  
Stefan Heinze ◽  
...  

AbstractBreaking the dilemma between small size and room-temperature stability is a necessary prerequisite for skyrmion-based information technology. Here we demonstrate by means of rate theory and an atomistic spin Hamiltonian that the stability of isolated skyrmions in ultrathin ferromagnetic films can be enhanced by the concerted variation of magnetic interactions while keeping the skyrmion size unchanged. We predict film systems where the lifetime of sub-10 nm skyrmions can reach years at ambient conditions. The long lifetime of such small skyrmions is due to exceptionally large Arrhenius pre-exponential factor and the stabilizing effect of the energy barrier is insignificant at room temperature. A dramatic increase in the pre-exponential factor is achieved thanks to the softening of magnon modes of the skyrmion, thereby increasing the entropy of the skyrmion with respect to the transition state for collapse. Increasing the number of skyrmion deformation modes should be a guiding principle for the realization of nanoscale, room-temperature stable skyrmions.


1961 ◽  
Vol 06 (03) ◽  
pp. 435-444 ◽  
Author(s):  
Ricardo H. Landaburu ◽  
Walter H. Seegers

SummaryAn attempt was made to obtain Ac-globulin from bovine plasma. The concentrates contain mostly protein, and phosphorus is also present. The stability characteristics vary from one preparation to another, but in general there was no loss before 1 month in a deep freeze or before 1 week in an icebox, or before 5 hours at room temperature. Reducing agents destroy the activity rapidly. S-acetylmercaptosuccinic anhydride is an effective stabilizing agent. Greatest stability was at pH 6.0.In the purification bovine plasma is adsorbed with barium carbonate and diluted 6-fold with water. Protein is removed at pH 6.0 and the Ac-globulin is precipitated at pH 5.0. Rivanol and alcohol fractionation is followed by chromatography on Amberlite IRC-50 or DEAE-cellulose. The final product is obtained by isoelectric precipitation.


2020 ◽  
Author(s):  
Katsuya Maruyama ◽  
Takashi Ishiyama ◽  
Yohei Seki ◽  
Kounosuke Oisaki ◽  
Motomu Kanai

A novel Tyr-selective protein bioconjugation using the water-soluble persistent iminoxyl radical is described. The conjugation proceeded with high Tyr-selectivity and short reaction time under biocompatible conditions (room temperature in buffered media under air). The stability of the conjugates was tunable depending on the steric hindrance of iminoxyl. The presence of sodium ascorbate and/or light irradiation promoted traceless deconjugation, restoring the native Tyr structure. The method is applied to the synthesis of a protein-dye conjugate and further derivatization to azobenzene-modified peptides.


1987 ◽  
Vol 52 (5) ◽  
pp. 1356-1361
Author(s):  
S. Abdel Rahman ◽  
M. Elsafty ◽  
A. Hattaba

The conformation of elastin-like peptides Boc-Ala-Pro-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Ala-Pro-Gly-Val-Gly-Val-APEGM, Boc-Ala-Pro-Gly-Val-Gly-Val-Ala-Pro-Gly-Val-Gly-Val-APEGM were examined in solution using circular dichroism at 30 °C, 50 °C, and 70 °C and in solid state by IR at room temperature. The studies show that the β-turn is a significant conformational feature for peptides under investigation in solution at 30 °C and 50 °C, but at 70 °C the tetra, hexa, and decapeptides show the CD feature characteristic of the β-structure while the dodecapeptide spectra show the presence of β-turn which indicates the stability of the β-turn at this chain length. The IR spectra show that in the solid state at room temperature all investigated peptides assume essentially a β-turn except the tetrapeptide which present evidence of antiparallel β-structure. The β-turn contribution in the IR spectra increases with the increase of the chain length of the peptide.


1956 ◽  
Vol 2 (3) ◽  
pp. 145-159 ◽  
Author(s):  
Joseph T Anderson ◽  
Ancel Keys

Abstract 1. Methods are described for the separation, by paper electrophoresis and by cold ethanol, of α- and β-lipoproteins in 0.1 ml. of serum, with subsequent analysis of cholesterol in the separated portions. 2. It is shown that both methods of separation yield separated fractions containing substantially the same amounts of cholesterol. 3. Detailed data are given on the errors of measurement for total cholesterol and for cholesterol in the separated lipoprotein fractions. 4. Studies are reported on the stability of cholesterol in stored serum and on paper electrophoresis strips. It is shown that simple drying on filter paper causes no change in cholesterol content and yields a product that is stable for many weeks at ordinary room temperature. 5. The sources of variability in human serum cholesterol values are examined and it is shown that spontaneous intraindividual variability is a much greater source of error than the errors of measurement with these methods.


1974 ◽  
Vol 96 (4) ◽  
pp. 1322-1327
Author(s):  
Shun Cheng ◽  
C. K. Chang

The buckling problem of circular cylindrical shells under axial compression, external pressure, and torsion is investigated using a displacement function φ. A governing differential equation for the stability of thin cylindrical shells under combined loading of axial compression, external pressure, and torsion is derived. A method for the solutions of this equation is also presented. The advantage in using the present equation over the customary three differential equations for displacements is that only one trial solution is needed in solving the buckling problems as shown in the paper. Four possible combinations of boundary conditions for a simply supported edge are treated. The case of a cylinder under axial compression is carried out in detail. For two types of simple supported boundary conditions, SS1 and SS2, the minimum critical axial buckling stress is found to be 43.5 percent of the well-known classical value Eh/R3(1−ν2) against the 50 percent of the classical value presently known.


Author(s):  
Rebekah J. Nixon ◽  
Sascha H. Kranen ◽  
Anni Vanhatalo ◽  
Andrew M. Jones

AbstractThe metabolic boundary separating the heavy-intensity and severe-intensity exercise domains is of scientific and practical interest but there is controversy concerning whether the maximal lactate steady state (MLSS) or critical power (synonymous with critical speed, CS) better represents this boundary. We measured the running speeds at MLSS and CS and investigated their ability to discriminate speeds at which $$\dot{V}{\text{O}}_{2}$$ V ˙ O 2 was stable over time from speeds at which a steady-state $$\dot{V}{\text{O}}_{2}$$ V ˙ O 2 could not be established. Ten well-trained male distance runners completed 9–12 constant-speed treadmill tests, including 3–5 runs of up to 30-min duration for the assessment of MLSS and at least 4 runs performed to the limit of tolerance for assessment of CS. The running speeds at CS and MLSS were significantly different (16.4 ± 1.3 vs. 15.2 ± 0.9 km/h, respectively; P < 0.001). Blood lactate concentration was higher and increased with time at a speed 0.5 km/h higher than MLSS compared to MLSS (P < 0.01); however, pulmonary $$\dot{V}{\text{O}}_{2}$$ V ˙ O 2 did not change significantly between 10 and 30 min at either MLSS or MLSS + 0.5 km/h. In contrast, $$\dot{V}{\text{O}}_{2}$$ V ˙ O 2 increased significantly over time and reached $$\dot{V}{\text{O}}_{2\,\,\max }$$ V ˙ O 2 max at end-exercise at a speed ~ 0.4 km/h above CS (P < 0.05) but remained stable at a speed ~ 0.5 km/h below CS. The stability of $$\dot{V}{\text{O}}_{2}$$ V ˙ O 2 at a speed exceeding MLSS suggests that MLSS underestimates the maximal metabolic steady state. These results indicate that CS more closely represents the maximal metabolic steady state when the latter is appropriately defined according to the ability to stabilise pulmonary $$\dot{V}{\text{O}}_{2}$$ V ˙ O 2 .


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Ramanshu P. Singh ◽  
Shakti Yadav ◽  
Giridhar Mishra ◽  
Devraj Singh

Abstract The elastic and ultrasonic properties have been evaluated at room temperature between the pressure 0.6 and 10.4 GPa for hexagonal closed packed (hcp) hafnium (Hf) metal. The Lennard-Jones potential model has been used to compute the second and third order elastic constants for Hf. The elastic constants have been utilized to calculate the mechanical constants such as Young’s modulus, bulk modulus, shear modulus, Poisson’s ratio, and Zener anisotropy factor for finding the stability and durability of hcp hafnium metal within the chosen pressure range. The second order elastic constants were also used to compute the ultrasonic velocities along unique axis at different angles for the given pressure range. Further thermophysical properties such as specific heat per unit volume and energy density have been estimated at different pressures. Additionally, ultrasonic Grüneisen parameters and acoustic coupling constants have been found out at room temperature. Finally, the ultrasonic attenuation due to phonon–phonon interaction and thermoelastic mechanisms has been investigated for the chosen hafnium metal. The obtained results have been discussed in correlation with available findings for similar types of hcp metals.


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