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11.
S. Zubė 《Lithuanian Mathematical Journal》1998,38(3):291-308
The main purpose of this paper is to study projective classes of bidegree (2,1) parametrizable surfaces in a real projective
3-space. It turns out that the implicit degree of such surfaces is two, three, or four, and singular curves have degree three.
We describe all possibilities for singular curves and pinch points on such surfaces. The presentation has been made from the
point of view of analytic geometry and does not presume a deep knowledge of algebraic geometry.
Partially supported by the Lithuanian State Science and Studies Foundation.
Vilnius University, Naugarduko 24, 2006 Vilnius, Lithuania. Published in Lietuvos Matematikos Rinkinys, Vol. 38, No. 3, pp.
379–402, July–September, 1998. 相似文献
12.
Remigijus Ivanauskas Ingrida Ancutienė Vitalijus Janickis Rūta Stokienė 《Central European Journal of Chemistry》2009,7(4):864-869
The process of obtaining semiconductive and electrical conductive layers of copper sulfides by the sorption — diffusion method
on polymers (polyamide 6 and low density polyethylene) using solutions of potassium pentathionate, K2S5O6, and higher polythionic acids, H2S
n
O6 (n = 21, 33), was investigated. The layers were characterized for compositional and electrical properties by X-ray diffraction
(XRD) analysis and sheet resistance measurements. The thickness of copper sulfides layers on polyamide and polyethylene increased
with increasing time of polymer sulfurization and varied from 10 to 43 μm. The variations of the sheet resistance of copper
sulfides layers formed on the surface of polymers on sulfurization agent used, the conditions of sulfurization, chemical and
phase composition of the obtained layers were established. Sheet resistance of copper sulfides layers decreases with increasing
time of the duration of sulfurization and the number of sulfur atoms in the polythionate anion. The sheet resistance values
for copper sulfide layers formed on the polyamide surface are much lower than those of Cu
x
S formed on the polyethylene surface. XRD showed the predomination of Cu
x
S phases with low x values.
相似文献
13.
Feliksas Ivanauskas Albertas Malinauskas Liana Stonkienė 《Journal of mathematical chemistry》2014,52(8):2020-2029
We extend our previous model taking into account a possible autoacceleration mechanism of electrochemical processes. It is supposed that protons generated in an electrochemical oxidation of ascorbate are responsible for an increase of electric conductivity of polyaniline. Accordingly, the current–time profiles have been calculated taking into account a “threshold” value for proton concentration to increase the electric conductivity of polyaniline by one or more orders of magnitude. Different kinds of corresponding profiles, including ones with a sigmoid character and possessing sharp current flashes as well, were obtained and analyzed. 相似文献
14.
K. Juodkazis J. Juodkazytė R. Vilkauskaitė V. Jasulaitienė 《Journal of Solid State Electrochemistry》2008,12(11):1469-1479
The processes of nickel surface anodic oxidation taking place within the range of potentials preceding oxygen evolution reaction
(OER) in the solutions of 1 M KOH, 0.5 M K2SO4, and 0.5 M H2SO4 have been analyzed in the present paper. Metallic nickel, thermally oxidized nickel, and black nickel coating were used as
Ni electrodes. The methods of cyclic voltammetry and X-ray photoelectron spectroscopy were employed. The study was undertaken
with a view to find the evidence of peroxide-type nickel surface compounds formation in the course of OER on the Ni electrode
surface. On the basis of experimental results and literature data, it has been suggested that in alkaline solution at E ≈ 1.5 V (RHE) reversible electrochemical formation of Ni(IV) peroxide takes place according to the reaction as follows: This reaction accounts for both the underpotential (with respect to ) formation of O2 from NiOO2 peroxide and also small experimental values of dE/dlgi slope (<60 mV) at low anodic current densities, which are characteristic for the two-electron transfer process. It has been
inferred that the composition of the γ-NiOOH phase, indicated in the Bode and revised Pourbaix diagrams, should be ∼5/6 NiOOH + ∼1/6
NiOO2. The schemes demonstrating potential-dependent transitions between Ni surface oxygen compounds are presented, and the electrocatalytic
mechanisms of OER in alkaline, acid, and neutral medium have been proposed. 相似文献
15.
Genovaitė Valiulienė Albina Žielienė Birutė Šimkūnaitė Leonas Naruškevičius Loreta Tamašauskaitė Tamašiūnaitė Vidas Pakštas Algis Selskis 《Journal of Solid State Electrochemistry》2010,14(2):203-212
The electrochemical behavior of Bi2S3 coatings in Watts nickel plating electrolyte was investigated using the cyclic voltammetry, electrochemical quartz crystal
microbalance, X-ray diffraction, and energy dispersive X-ray analysis methods. During the bismuth sulfide coating reduction
in Watts background electrolyte in the potential region from −0.4 to −0.6 V, the Bi2S3 and Bi(III) oxygen compounds are reduced to metallic Bi, and the decrease in coating mass is related to the transfer of S2− ions from the electrode surface. When the bismuth sulfide coating is reduced in Watts nickel plating electrolyte, the observed
increase in coating mass in the potential region −0.1 to −0.4 V is conditioned by Ni2+ ions reduction before the bulk deposition of Ni, initiated by Bi2S3. In this potential region, the reduction of Bi(III) oxygen compounds can occur. After the treatment of as-deposited bismuth
sulfide coating in nickel plating electrolyte at E = −0.3 V, the sheet resistance of the layer decreases from 1013 to 500–700 Ω cm. A metal-rich mixed sulfide Ni3Bi2S2–parkerite is obtained when as-deposited bismuth sulfide coating is treated in Watts nickel plating electrolyte at a potential
close to the equilibrium potential of the Ni/Ni2+ system and then annealed at temperatures higher than 120 °C. 相似文献
16.
Vilija Pautienienė Loreta Tamašauskaitė-Tamašiūnaitė Aloyzas Sudavičius Giedrius Stalnionis Zenonas Jusys 《Journal of Solid State Electrochemistry》2010,14(9):1675-1680
Spontaneous modification of polycrystalline Pt by irreversibly adsorbed bismuth was performed in BiCl3 solution in concentrated hydrochloric acid under open-circuit conditions. After spontaneous modification, followed by extensive
rinsing with water and drying, the surface was characterized using X-ray photoelectron spectroscopy and electrochemistry.
Bi-oxy(chloride), oxide species, and metallic Bi were found at a submonolayer coverage on the Pt surface after spontaneous
modification. The electrochemical response of Bi-modified polycrystalline Pt electrode in sulfuric acid solution exhibits
a complex multi-peak feature, which is resulting in about constant redox charge (Bi species coverage) in the potential region
from 0 to 0.9 V (vs. a standard hydrogen electrode). The spontaneously Bi-modified Pt catalyst in model studies exhibits a
superior activity towards formic acid oxidation at fuel cell anode relevant potentials. The catalytic effect of bismuth oxy-species
is explained in terms of both inhibition of COad formation and oxidation of COad in reaction with Bi-oxy-species. 相似文献
17.
Mažeikienė R Niaura G Eicher-Lorka O Malinauskas A 《Journal of colloid and interface science》2011,357(1):189-197
Surface-enhanced Raman spectroscopy (SERS) was used to probe the structure of adsorbed and electropolymerized Meldola blue (MB) films on roughened gold surfaces in solutions with pH 1.0 and 7.0 by using 785 nm excitation wavelength. Spectral bands were assigned based on density functional theory (DFT) calculations at B3LYP/6-311+G(2d, p) level. The most characteristic band of the oxidized MB form was found to be the breathing vibration of the central ring containing heteroatoms at 596 cm(-1). Based on a red shift of bands assigned to vibrations of double C=N(C(2)H(6)) bonds and adjacent ring C=C bonds in surface spectra as compared with solution 1 it was suggested that polymerization and interaction with an electrode surface proceed through these moieties. The presence of out-of-plane bands in SERS spectra was attributed to "flat" or slightly "tilted" orientation of aromatic rings at the interface. Potential-dependent spectral changes were followed by SERS spectroscopy. Raman spectra of the reduced MB form were obtained in both pH 1.0 and pH 7.0 solutions by analysis of the potential-difference SERS spectra. Reduced MB form can be recognized by characteristic bands near 1620, 1574, 1374, and 1234 cm(-1). By comparing the intensities of 1637 cm(-1) (oxidized MB form) and 1374 cm(-1) (reduced MB form) bands in experimental spectra of polymerized MB in pH 1.0 solution, a reduction-induced decrease by factor of 7 was estimated. A similar tendency in intensity changes showed calculations indicating that this effect is associated with reduction-induced changes in the molecular structure of the dye. 相似文献
18.
Downward flux of stratospheric ozone contributes to the near ground level ozone concentrations. The intensity, amount of vertical
ozone flow can be evaluated by the ratio of two cosmogenic radionuclides (33P/32P, 7Be/32P). Some examples presented in this paper are demonstrating the possibilities of this method. The application of tracer method
makes evident the seasonal variations (with maxima during the spring — summer months and minima during winter) of the amount
of stratospheric ozone in the ground air. Average monthly contribution from stratospheric ozone in the lower level of the
atmosphere ranged from 0 to 18% in 1998–99. During short term intervals (2–3 days) the amount of the stratospheric ozone can
increase up to ∼90%. 相似文献
19.
20.
Žydrė Šaltienė Natalija Jatulienė Mudis Šalkauskas Daiva Brukštienė Asta Ruzgytė Aušra Tarasevičiūtė Julius Kalibatas 《Accreditation and quality assurance》2005,10(8):444-451
The estimation scheme of uncertainty of determination of 1-hydroxypyrene (1-OHP) in urine was developed analysing the main
stages of the analytical procedure: (1) preparation of 1-OHP standards, (2) creation of the calibration curve for the high
performance liquid chromatography (HPLC) analysis method with the evaluation of recovery, (3) measuring procedure of aliquot
of urine, (4) adjusting the pH of aliquot and hydrolysis with enzyme, (5) solid phase extraction, (6) concentration of the
extract, (7) injection of the extract to chromatograph and analysing by the HPLC method, (8) calculation of 1-OHP mass from
the calibration curve, (9) calculation of 1-OHP concentration in urine. The evaluation of the uncertainty is based on quantification
of individual components. Combined uncertainty was calculated using the law of propagation of uncertainties according to the
EURACHEM/CITAC guidelines. Level dependence of the uncertainty arises from the calibration curve.
The limits of detection and quantification were found to be equal to 0.03 and 0.1 ng/mL, respectively. The calculated expanded
level-dependent uncertainty covers 47–27–25% within the concentration range 0.03–0.1–0.4 ng/mL with the materials and equipment
used. These parameters could easily be recalculated according to the proposed scheme if there are some changes in the analysis
procedure. 相似文献