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11.
A textured pellet of YBa2Cu3O7?δ was prepared and doped with57Co. After subsequent heat treatments the cobalt was found at the two copper sites. The degree of alignment of individual crystallites (about 40%) was determined from the Mössbauer spectrum by using a method developed by the authors [1]. The same method showed that the most characteristic doublet component of such spectra (δ=0.08 mm/s; |ΔE Q|=1.96 mm/s) is associated with a site, most probably a Cu(1) site, where the EFG is parallel to thec direction of the unit cell. The sign ofV zz turned out to be negative, giving a negative quadrupole splitting (ΔE Q=?1.96 mm/s) for that component. 相似文献
12.
Dipak Ghosh Madhumita Lahiri Argha Deb Susobhan Das Krishnadas Purkait Biswanath Biswas Jayanta Roy Choudhury Rini Chatterjee Abdul Kayum Jafry 《Zeitschrift fur Physik C Particles and Fields》1996,71(1):243-249
The scaled factorial moments and the multifractal moments have been investigated in differentη-intervals to study the dynamical fluctuation of pions produced in 200 AGeV32S-Ag/Br interaction. In order to investigate the detail characteristics of intermittency behaviour, theF-moments are extracted up to the eighth order of moments in differentM-intervals. The analysis indicates a non-thermal phase transition and different regime of particle production during the hadronisation process. 相似文献
13.
Transverse flow transversely excited (TFTE) CO2 lasers are easily scalable to multikilowatt level. The laser power can be scaled up by increasing the volumetric gas flow
and discharge volume. It was observed in a TFTE CW CO2 laser having single row of pins as an anode and tubular cathode that the laser power was not increasing when the discharge
volume and the gas volumetric flow were increased by increasing the electrode separation keeping the gas flow velocity constant.
The discharge voltage too remained almost constant with the change of electrode separation at the same gas flow velocity.
This necessitated revision of the scaling laws for designing this type of high power CO2 laser. Experimental results of laser performance for different electrode separations are discussed and the modifications
in the scaling laws are presented. 相似文献
14.
15.
16.
Kinetics of the copolymerisation of styrene and maleic anhydride have been studied in dioxane at 50° using azobisisobutyronitrile as initiator. Explanation of the kinetic behaviour has been attempted in terms of the participation in propagation of a charge-transfer complex between the monomers along with propagation via free monomers. It is found that the complex model is able to explain most features of the copolymerisation of these monomers. It has been possible to determine the constants δ1, δ2, k1c/k12, k2c/k21 and Φ where k1c/k12 and k2c/k21 represent the specific rate constants of reaction of a particular type of radical with a dissimilar monomer site of the complex relative to that with a dissimilar free monomer. They are reviewed on the basis of available literature data. The cross-termination factor Φ is found to play an important role in the present system. An approximate value of for maleic anhydride could also be found and this probably represents the first reported value for this constant from copolymerisation. The applicability of the generalised penultimate model is also briefly discussed. 相似文献
17.
Eldefrawi ME Azer NL Nath N Anis NA Bangalore MS O'Connell KP Schwartz RP Wright J 《Applied biochemistry and biotechnology》2000,87(1):25-35
An automated flow fluorometer designed for kinetic binding analysis was adapted to develop a solid-phase competitive fluoroimmunoassay
for urinalysis of opiates. The solid phase consisted of polymer beads coated with commercial monoclonal antibodies (MAbs)
raised against morphine. Fluorescein-conjugated morphine (FL-MOR) was used as the fluorescein-labeled hapten. The dissociation
equilibrium constant (K
D
) for the binding of FL-MOR to the anti-MOR MAb was 0.23 nM. The binding of FL-MOR to the anti-MOR MAb reached steady state within minutes and was displaced effectively by morphine
and other opiates. Morphine-3-glucuronide (M3G), the major urinary metabolite of heroin and morphine, competed effectively
with FL-MOR in a concentration-dependent manner for binding to the antimorphine MAb and was therefore used to construct the
calibration curve. The sensitivity of the assay was 0.2 ng/mL for M3G. The assay was effective at concentrations of M3G from
0.2 to 50 ng/mL, with an IC50 of 2 ng/mL. Other opiates and heroin metabolites that showed >50% crossreactivity when present at 1 μg/mL included codeine,
morphine-6-glucuronide, and oxycodone. Methadone showed very low crossreactivity (<5%), which is a benefit for testing in
patients being treated for opiate addictions. The high sensitivity of the assay and the relatively high cutoff value for positive
opiate tests allows very small sample volumes (e.g., in saliva or sweat) to be analyzed. A double-blind comparison using 205
clinical urine samples showed good agreement between this single-step competitive assay and a commercially performed enzyme
multiplied immunoassay technique for the detection of opiates and benzoylecgonine (a metabolite of cocaine). 相似文献
18.
The catalytic activity of Chromobacterium viscosum lipase (CV-lipase) was estimated across varying surfactant tail lengths (C-10-C-18) in water-in-oil (w/o) microemulsions of cationic surfactants containing four different hydroxyethyl-substituted head groups. An attempt to find a correlation, if any, between the activity of interfacially solubilized lipase and the varying surfactant tails was made for the first time in micellar enzymology. The second-order rate constant, k2, in lipase-catalyzed hydrolysis of p-nitrophenyl-n-hexanoate at pH 6.0 and 25 degrees C shows an improvement in enzyme activity (approximately 30-140%) across different head groups of amphiphiles with increasing tail lengths in varying solution compositions. Improvement of enzyme activity is prominent in ascending from C-10 to C-14/C-16, depending on the nature of polar head group. The hydrolytic activity of lipase in different surfactant (50 mM)/water/isooctane/n-hexanol with varying z= [alcohol]/[surfactant] (6.4 or 4.8) was amplified by 25-250% with increment in surfactant tail length in comparison with widely used cationic w/o microemulsions having solution compositions (z=16). As a notable outcome of this research, we found w/o microemulsions of 25 mM tetradecyltrimethylammonium bromide/water/isooctane/n-hexanol (z=8) producing the highest ever activity of lipase in any w/o microemulsions. 相似文献
19.
The emission Mössbauer spectra of 125I labeled iodobenzene, methyl iodide, and of their dilute solutions in benzene and hexane, were computer analyzed. Two species were observed, in one of which tellurium is presumably attached to two organic moieties, while in the other, tellurium is attached to a single organic moiety. 相似文献
20.
The change in optical properties of colloidal gold upon aggregation has been used to develop an experimentally convenient colorimetric method to study the interfacial phase transition of an elastin-like polypeptide (ELP), a thermally responsive biopolymer. Gold nanoparticles, functionalized with a self-assembled monolayer (SAM) of mercaptoundecanoic acid onto which an ELP was adsorbed, exhibit a characteristic red color due to the surface plasmon resonance (SPR) of individual colloids. Raising the solution temperature from 10 degrees C to 40 degrees C thermally triggered the hydrophilic-to-hydrophobic phase transition of the adsorbed ELP resulting in formation of large aggregates due to interparticle hydrophobic interaction. Formation of large aggregates caused a change in color of the colloidal suspension from red to violet due to coupling of surface plasmons in aggregated colloids. The surface phase transition of the ELP was reversible, as seen from the reversible change in color upon cooling the suspension to 10 degrees C. The formation of colloidal aggregates due to the interfacial phase transition of adsorbed ELP was independently verified by dynamic light scattering of ELP-modified gold colloids as a function of temperature. Colloidal SPR provides a simple and convenient colorimetric method to study the influence of the solution environment, interfacial properties, and grafting method on the transition properties of ELPs and other environmentally responsive polymers at the solid-water interface. 相似文献