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91.
Optically clear glasses of SrBi2B2O7 (SBBO) were fabricated via the conventional melt-quenching technique. The amorphous nature of the as-quenched samples of this compound was confirmed by X-ray powder diffraction (XRD) studies. Its glassy nature was established by differential scanning calorimetry (DSC). However, the optical microscopy revealed the presence of isolated hexagonal shaped crystallites especially at the edges of the as-quenched glasses. The glass plates that were heat-treated around the onset of the glass transition temperature (670 K) for 12 h yielded transparent (~60% transmission) glass-ceramics of SrBi2B2O7 (SBBO) with well defined microstructure. These were found to be textured associated with an orientation factor of about 0.77 (77%). The optical transmission studies carried out in the 100–1200 nm wavelength range confirmed both the as-quenched and heat-treated samples to be transparent from 400 to 1200 nm. The dielectric properties of the as-quenched as well as the heat-treated (670 K/12 h) samples were studied as a function of frequency (100 Hz–10 MHz) at various temperatures (303–873 K). The dielectric dispersion at higher temperatures in the as-quenched glass was rationalized using Jonscher’s dielectric dispersion relations. The prefactor A(T) and the exponent n(T) in the Jonscher’s expression were found to be maximum and minimum respectively around the crystallization temperature (Tcr) of the as-quenched SBBO glasses. 相似文献
92.
Mesoscopic density fluctuations in liquid phase sintered silicon carbide have been investigated using small angle neutron
scattering (SANS). The increase in the additives results in the modification in the pore size distribution and to some extent
the total porosity. SANS revealed a mass fractal nature of the agglomerated matrix microstructure. The fractal dimension of
the matrix does not change appreciably with the additives although the upper cut-off value of the fractal decreases significantly
with the increase in the additives. The liquid phase sintering due to the presence of additives helps to achieve higher level
of densification. However, the agglomeration hinders achievement of the fully dense pellets.
相似文献
93.
Kallol Mukherjee Nicolas Grimblat Somratan Sau Koushik Ghosh Majji Shankar Vincent Gandon Akhila K. Sahoo 《Chemical science》2021,12(44):14863
A direct Pd(ii)-catalyzed kinetic resolution of heteroaryl-enabled sulfoximines through an ortho-C–H alkenylation/arylation of arenes has been developed. The coordination of the sulfoximine pyridyl-motif and the chiral amino acid MPAA ligand to the Pd(ii)-catalyst controls the enantio-discriminating C(aryl)–H activation. This method provides access to a wide range of enantiomerically enriched unreacted aryl-pyridyl-sulfoximine precursors and C(aryl)–H alkenylation/arylation products in good yields with high enantioselectivity (up to >99% ee), and selectivity factor up to >200. The coordination preference of the directing group, ligand effect, geometry constraints, and the transient six-membered concerted-metalation–deprotonation species dictate the stereoselectivity; DFT studies validate this hypothesis.A Pd/MPAA catalysed KR of heteroaryl substituted sulfoximines through C–H alkenylation and arylation (up to >99% ee) is developed. In-depth DFT studies uncover the salient features. 相似文献
94.
Suresh K. Chamarthi Brian Raterman Ria Mazumder Anthony Michaels Veeral M. Oza James Hanje Bradley Bolster Ning Jin Richard D. White Arunark Kolipaka 《Magnetic resonance imaging》2014
Magnetic resonance elastography (MRE) of the liver is a novel noninvasive clinical diagnostic tool to stage fibrosis based on measured stiffness. The purpose of this study is to design, evaluate and validate a rapid MRE acquisition technique for noninvasively quantitating liver stiffness which reduces by half the scan time, thereby decreasing image registration errors between four MRE phase offsets. In vivo liver MRE was performed on 16 healthy volunteers and 14 patients with biopsy-proven liver fibrosis using the standard clinical gradient recalled echo (GRE) MRE sequence (MREs) and a developed rapid GRE MRE sequence (MREr) to obtain the mean stiffness in an axial slice. The mean stiffness values obtained from the entire group using MREs and MREr were 2.72 ± 0.85 kPa and 2.7 ± 0.85 kPa, respectively, representing an insignificant difference. A linear correlation of R2 = 0.99 was determined between stiffness values obtained using MREs and MREr. Therefore, we can conclude that MREr can replace MREs, which reduces the scan time to half of that of the current standard acquisition (MREs), which will facilitate MRE imaging in patients with inability to hold their breath for long periods. 相似文献
95.
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98.
Zhang Chuanlun Liu Shi Logan John Mazumder Raja Phelps Tommy J. 《Applied biochemistry and biotechnology》1996,57(1):923-932
Applied Biochemistry and Biotechnology - An unusual thermophilic bacterium has been isolated from deep subsurface sediments and tested for its ability to enhance Fe(III), Co(III), and Cr(VI)... 相似文献
99.
Pritikana Khan P. S. Mazumder A. S. Ghosh 《Zeitschrift für Physik A Hadrons and Nuclei》1984,318(1):19-23
Scattering of positrons by hydrogen-like-ions (He+, Li2+, Be3+ and B4+) has been studied using two variants of the polarized orbital method. The positronium formation channel has not been included in the calculations,s-wave phase shifts obtained using the two variants differ appreciably from each other. Moreover, the polarized orbitals-wave phase shifts fore +-B4+ scattering differ from the corresponding variational results qualitatively in the low energy region. The differential cross sections are reported. 相似文献
100.
Delta(5)-3-Ketosteroid Isomerase (KSI) catalyzes the isomerization of 5,6-unsaturated ketosteroids to their 4,5-unsaturated isomers at a rate approaching the diffusion limit. The isomerization reaction follows a two-step general acid-base mechanism starting with Asp38-CO(2)(-) mediated proton abstraction from a sp(3)-hybridized carbon atom, alpha to carbonyl group, providing a dienolate intermediate. In the second step, Asp38-CO(2)H protonates the C6 of the intermediate providing a 4,5-unsaturated ketosteroid. The details of the mechanism have been highly controversial despite several experimental and computational studies of this enzyme. The general acid-base catalysis has been proposed to involve either a catalytic diad or a cooperative hydrogen bond mechanism. In this paper, we report our results from the 1.5 nanosecond molecular dynamics (MD) simulation of enzyme bound natural substrate (E.S) and enzyme bound intermediate (E.In) solvated in a TIP3P water box. The final coordinates from our MD simulation strongly support the cooperative hydrogen bond mechanism. The MD simulation of E.S and E.In shows that both Tyr14 and Asp99 are hydrogen bonded to the O3 of the substrate or intermediate. The average hydrogen bonding distance between Tyr14-OH and O3 becomes shorter and exhibits less fluctuation on E.S --> E.In. We also observe dynamic motions of water moving in and out of the active site in the E.S structures. This free movement of water disappears in the E.In structures. The active site is shielded by hydrophobic residues, which come together and squeeze out the waters from the active site in the E.In complex. 相似文献