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561.
Effects of anionic and cationic micelles on the oxidation of d-dextrose by diperiodatoargentate(III)
Mohd Yusuf Dar Mohammad Ilyas Parveen Kumar Zaheer Khan 《Colloid and polymer science》2006,285(3):315-321
The oxidative behavior of d-dextrose toward diperiodatoargentate(III) (DPA) has been studied in the absence and presence of anionic and cationic micelles of sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB), respectively. The kinetics is based on the reduction of silver(III) to silver(I) by d-dextrose under pseudo-first-order conditions. The monoperiodatoargentate(III) ions act as active oxidants in comparison to that of DPA. The reactions are first- and fractional-order dependence with respect to [DPA] and [d-dextrose], respectively. The reaction rates decrease with [H+] and [periodate]. The premicellar environment of SDS and CTAB strongly inhibits the reaction rate. Inhibition is due to favorable thermodynamic/electrostatic binding between the Ag(III) complex and CTAB monomer aggregates. A suitable mechanism involving a one-electron transfer (rate-determining step) from d-dextrose to the silver(III) species has been proposed. Activation parameters have been evaluated and discussed. 相似文献
562.
We consider the generalized shift operator associated with the Laplace-Bessel differential operator $$ \Delta _B = \sum\limits_{i = 1}^n {\frac{{\partial ^2 }} {{\partial x_j^2 }}} + \sum\limits_{i = 1}^k {\frac{{\gamma _i }} {{x_i }}\frac{\partial } {{\partial x_i }}} $$ , and study the modified B-Riesz potential ? α, β generated by the generalized shift operator acting in the B-Morrey space in the limiting case. We prove that the operator ? α, β, 0 < α < n + |γ|, is bounded from the B-Morrey space L (n+|γ|?λ)/α,λ,γ (? k,+ n ) to the B-BMO space BMO γ (? k,+ n ). 相似文献
563.
P. K. Manna S. M. Yusuf M. D. Mukadam J. Kohlbrecher 《Applied Physics A: Materials Science & Processing》2012,109(2):385-390
We report the evidence of a core?Cshell structure in the antiferromagnetic La0.2Ce0.8CrO3 nanoparticles by using a combination of neutron diffraction, polarized neutron small angle scattering (SANSPOL), and dc magnetization techniques. The neutron diffraction study establishes that the present nanoparticles are antiferromagnetic in nature. The magnetic scattering in the SANSPOL study arises from the shell part of the nanoparticles due to the disordered surface spins. The analysis of the SANSPOL data shows that these nanoparticles have a mean core diameter of 12.3±1.1?nm, and a shell thickness of 2.8±0.4?nm, giving a core?Cshell structure with an antiferromagnetic core, and a shell with a net magnetic moment under an applied magnetic field. 相似文献
564.
The Ising model with quenched random magnetic fields is examined for single Gaussian, bimodal and double Gaussian random field distributions by introducing an effective field approximation that takes into account the correlations between different spins that emerge when expanding the identities. Random field distribution shape dependence of the phase diagrams, magnetization and internal energy is investigated for a honeycomb lattice with a coordination number q=3. The conditions for the occurrence of reentrant behavior and tricritical points on the system are also discussed in detail. 相似文献
565.
Dynamic behavior of a site diluted Ising ferromagnet in the presence of a periodically oscillating magnetic field has been analyzed by means of the effective field theory (EFT). The dynamic equation of motion has been solved for a honeycomb lattice (z=3) with the help of a Glauber type stochastic process. The global phase diagrams and the variation of the corresponding dynamic order parameter as a function of the Hamiltonian parameters and temperature has been investigated in detail and it has been shown that the system exhibits reentrant phenomena, as well as a dynamic tricritical point which disappears for sufficiently weak dilution. 相似文献
566.
Photoinduced Crosslinking of Polymers Containing Pendant Hydroxyl Groups by Using Bisbenzodioxinones
In the present study, it has been demonstrated that polymers containing pendant hydroxyl groups can undergo photoinduced crosslinking upon irradiation in the presence of bifunctional benzodioxinone. Irradiation of the copolymers of 2‐hydroxyethyl methacrylate (HEMA) and methyl methacrylate (MMA) in dichloromethane and THF solutions or in films containing bisbenzodioxinone, namely 5‐[9‐(4‐oxo‐2,2‐diphenyl‐4H‐benzo[d][1,3]dioxin‐5‐yloxy) nonyloxy]‐2,2‐diphenyl‐4H‐benzo[d][1,3]dioxin‐4‐one resulted in the formation of insoluble networks. Model studies using monofunctional napthodioxinone, namely 7‐hydroxy‐2,2‐diphenyl‐4H‐naphtho[2,3‐d][1,3]dioxin‐4‐one, revealed that crosslinking occurs via inter‐chain ester formation between photochemically generated keten intermediates and pendant hydroxyl groups.
567.
IntroductionPfaff[1]hasbeendefinedaquaternionproductonleaf (theplanecontainingtheOx_axis) .Byaidoftheproduct,anewproductisdefinedonplaneswhichpassesthroughtheorigindonotcontaintheOx_axisandsomeofthepropertiesofthisproducthavebeeninvestigated .Agrawal[2 ]gavesomealgebricpropertiesofHamiltonoperators.Also ,quaternionswereexpressedintermsof 4× 4matricesbymeansoftheseoperators.Yayli[3]gavehomotheticmotionswithaidoftheHamiltonoperatorsatE4 .Hacisalihoglu[4 ]showedthatallHomotheticmotionsinn_di… 相似文献
568.
W. L. Rigot M. E. Buchmann T. J. Quinn J. D. Romick S. O. Yusuf 《Journal of Radioanalytical and Nuclear Chemistry》2000,243(1):205-208
The role of neutron activation analysis (NAA) at The Dow Chemical Company has not changed significantly since the first operations, which were conducted in July, 1967. That role is threefold; provide results with appropriate precision, accuracy and sensitivity; provide results in a timely manner; and provide results for a reasonable cost. What has changed, are the requirements for satisfying each of the three components of the role. In a business-focused environment, analyses need to be performed faster with better sensitivity and/or precision and be more cost efficient. In order to meet these requirements, operations at The Dow TRIGA Research Reactor are devoted to NAA activities. 相似文献
569.
The lead concentrations of the fruit samples were determined by using slotted tube atom trap (STAT)-enrichment-flame and graphite furnace atomic absorption spectrometry (FAAS and GF-AAS). The soil samples related to these fruits were also analysed for Pb after extraction with various chemical reagents. The relation between the fruit-lead and soil-extractable lead concentrations was examined in order to explain the bioavailability of lead. A linear relation was observed between the hot Na2EDTA extraction-soluble Pb contents in the soil and the Pb concentrations in the mulberry (R2=0.95), strawberry and apple grown on these soils. Probable chemical forms of lead in soil were evaluated. Acceptable agreement (at least 91%) was achieved between the results of STAT-enrichment-FAAS and GF-AAS. 相似文献
570.
Ioan Cianga Takamichi Senyo Koichi Ito Yusuf Yagci 《Macromolecular rapid communications》2004,25(19):1697-1702
Summary: The possibility of transforming a living anionic polymerization into a stable radical‐mediated radical polymerization (SFRP) was demonstrated. For this purpose, 2,2,6,6‐tetramethylpiperidine‐N‐oxyl (TEMPO) alcoholate, formed by a one‐electron redox reaction between potassium naphthalene and TEMPO, was used to initiate the living anionic polymerization of ethylene oxide (EO). Poly(ethylene oxide) obtained in this way possessed TEMPO terminal units and was subsequently used as an initiator for the SFRP of styrene to give block copolymers.