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81.
V. V. Dvorkin N. N. Dzbanovskii A. F. Pal’ N. V. Suetin A. Yu. Yur’ev P. Ya. Detkov 《Physics of the Solid State》2004,46(4):729-732
A suspension of ultrafine-dispersed nanodiamond was used for introducing (in particular, selectively) high-density centers of diamond nucleation on various substrates. High-quality doped diamond films to be used as electrochemistry electrodes were deposited from the gas phase in a microwave discharge on certain substrates treated using ultrafine-dispersed nanodiamond. A uniform distribution of nucleation centers with concentrations greater than 1010 cm-2 on silicon substrates was obtained. Electrochemical current-potential curves were measured for continuous films. Diamond meshes of different transparency were grown using selective nucleation. Successful production of high-quality doped diamond meshes gives grounds to consider them the most promising electrodes for use in electrochemistry. 相似文献
82.
Russian Physics Journal - 相似文献
83.
84.
Results of a numerical analysis of mass transfer in systems of macroscopic particles with various isotropic interaction potentials are presented. Parameters that determine transport properties of nonideal dissipative systems are obtained for a broad class of model potentials. An approximate expression for the diffusivity of interacting particles is proposed. The relationship between diffusivity and viscosity is analyzed for strongly nonideal systems. 相似文献
85.
E. A. Ekimov E. L. Gromnitskaya D. A. Mazalov A. F. Pal’ V. V. Pichugin S. Gierlotka B. Palosz J. A. Kozubowski 《Physics of the Solid State》2004,46(4):755-757
Superhard nanodiamond-SiC ceramics are prepared by infiltrating liquid Si into porous nanodiamond compacts under pressure.
Synthesized samples are 2.2 mm thick and 3–4 mm in diameter. The effect of particle size of dynamically synthesized nanodiamond
powders on silicon infiltration and SiC phase formation is studied. It is established that silicon does not penetrate into
the pores of nanodiamond powders if the original particle size is smaller than 0.5–1.0 μm. The critical pore size for infiltration
is 100–200 nm. A study of the microstructure of the samples showed the presence of the nanometer-and submicron-scale SiC phase.
The ultrasound velocities are measured in the prepared compacts, and the elastic moduli are calculated.
__________
Translated from Fizika Tverdogo Tela, Vol. 46, No. 4, 2004, pp. 734–736.
Original Russian Text Copyright ? 2004 by Ekimov, Gromnitskaya, Mazalov, Pal’, Pichugin, Gierlotka, Palosz, Kozubowski. 相似文献
86.
87.
M. I. Adamovich V. Bradnova S. Vokal S. G. Gerasimov V. A. Dronov P. I. Zarubin A. D. Kovalenko K. A. Kotel'nikov V. A. Krasnov V. G. Larionova F. G. Lepekhin A. I. Malakhov G. I. Orlova N. G. Peresadko N. G. Polukhina P. A. Rukoyatkin V. V. Rusakova N. A. Salmanova B. B. Simonov M. M. Chernyavsky M. Haiduc S. P. Kharlamov L. Just 《Physics of Atomic Nuclei》2004,67(3):514-517
New results concerning the topology of the fragmentation of relativistic nuclei 7Li and 10B are presented. A program is proposed for studying the cluster structure of stable and radioactive nuclei. The use of emulsions in the investigation of nuclear clustering in the fragmentation of light nuclei at energies are in excess of 1 GeV per nucleon is discussed. 相似文献
88.
Stacy J. Taylor Robson F. Storey 《Journal of polymer science. Part A, Polymer chemistry》2004,42(23):5942-5953
3,3′,5,5′‐Tetrakis(2‐chloro‐2‐propyl)biphenyl (biphenyl tetracumyl chloride, BPTCC) and 1,3‐bis[3,5‐bis(2‐chloro‐2‐propyl)phenoxy]propane (diphenoxypropane tetracumyl chloride, DPPTCC) were synthesized as initiators for quasiliving cationic polymerization of isobutylene (IB). In the synthesis of BPTCC, tetrafunctionality was achieved via the coupling of dimethyl 5‐bromoisophthalate (DMBI) using nickel dibromide bis(triphenylphosphine) and zinc in the presence of a base; in the synthesis of DPPTCC, two equivalents of dimethyl 5‐hydroxyisophthalate were linked via reaction with 1,3‐dibromopropane in the presence of potassium carbonate. Both initiators were used to initiate the polymerization of IB under quasiliving cationic polymerization conditions. PIB initiated from BPTCC revealed a chain end/molecule value (as determined by 1H‐NMR) of 3.85, verifying the nearly exclusive production of 4‐arm polyisobutylene (PIB). GPC analysis revealed a narrow peak representing the target four‐arm PIB, with a slight shoulder at high elution volumes (low molecular weights). GPC analysis of the PIB initiated by DPPTCC revealed multimodal distributions, suggesting the formation of two‐, three‐, and four‐arm star polymers during the polymerization. This behavior was attributed to Friedel–Crafts alkylation of the initiator core after the addition of one IB unit, which was activated by the electron‐donating oxytrimethyleneoxy linking moiety. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5942–5953, 2004 相似文献
89.
Large melting point depressions for organic nanocrystals, in comparison with those of the bulk, were observed in an associative polymer: telechelic, pyrene‐labeled poly(dimethylsiloxane) (Py‐PDMS‐Py). Nanocrystals formed within nanoaggregates of pyrenyl units that were immiscible in poly(dimethylsiloxane). For 5 and 7 kg/mol Py‐PDMS‐Py, physical gels resulted, with melting points exceeding 40 °C and with small‐angle X‐ray scattering peaks indicating that the crystals were nanoconfined, were 2–3 nm long, and contained roughly 18–30 pyrenyl dye end units. In contrast, 30 kg/mol Py‐PDMS‐PY was not a gel and exhibited no scattering peak at room temperature; however, after 12 h of annealing at ?5 °C, multiple melting peaks were present at 5–30 °C. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3470–3475, 2004 相似文献
90.
J. Saunier F. Alloin J. Y. Sanchez B. Barrire 《Journal of Polymer Science.Polymer Physics》2004,42(3):544-552
Some microporous poly(vinylidene fluoride) (PVdF) separators for lithium‐ion batteries, used in liquid organic electrolytes based on a mixture of carbonate solvents and lithium salt LiPF6, were characterized by the study of the swelling phenomena on dense PVdF membranes. Various aspects of the kinetics of the carbonate solvents and the solvent mixture sorption in dense PVdF slabs were studied at different temperatures. Non‐Fickian behavior, characterized by S‐shaped sorption curves, was highlighted, and a salt effect, which resulted in two‐stage sorption, was studied. Diffusion coefficients and activation energies were calculated for the Fickian portions of the sorption curves, that is, at short times and low swelling ratios. A strong influence of the different interaction parameters was shown for the swelling kinetics. This study proved that the swelling of microporous PVdF membranes could be considered instantaneous. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 544–552, 2004 相似文献