共查询到20条相似文献,搜索用时 31 毫秒
1.
Employing the electrochemical cells with the solid oxide electrolyte the equilibrium oxygen potential in the pseudobinary Te-TeO2, Sb2O3-Sb2O4 and in the Sb2O3-Sb2O4-Te pseudoternary systems was determined in the temperature range 700-1173 K. In addition, the pseudobinary sections Sb2O3-Te, Sb2O3-Sb2O4 (1:1)-Te and Sb2O4-Te were examined by DTA in the temperature range 500-1300 K. Using these results the evolution of the pseudoternary system with temperature can be suggested. It was found that, at 718 K, a ternary eutectic with a composition close to pure Te appears in the system. At a higher temperature, 920 K, another liquid phase is formed, which is characteristic of the ternary four-phase equilibrium L2 + Sb2O4(s) + Sb2O3(s) = L1. 相似文献
Kanthal + Re, Te(l), TeO2(s)O−2 air, Pt
Pt + Re, Sb2O3(s), Sb2O4(s)O−2 air, Pt
Pt + Re, Sb2O3(s), Sb2O4(s), Te(l)O−2 air, Pt
2.
The intermolecular potential function of Smith–Thakkar type for C60 has been proposed, and its expression is as followsThe unit of u(r) is J/mol, r is the distance between two C60 molecules center and the unit is nm. Some properties of C60 in the gas and crystal have been studied using the interaction potential of Smith–Thakkar type, such as stability of C60 crystals, virial coefficient and lattice dynamics. 相似文献
3.
Line sources with slab shields represent typical source–shield configurations in gamma-ray attenuation problems. Such shielding problems often lead to the generalized secant integrals of the formRecently, the author has developed rapidly convergent infinite-series representation of generalized secant integrals involving incomplete gamma functions. The validity of this representation was established for zero and positive values of the integral parameter a (a0). In this paper the definition is extended to include negative real a values. It is demonstrated that the introduced series representation is still valid. In addition, general recurrence relations are established that allow precise calculation of the integral for negative a values. 相似文献
4.
In this paper we continue the investigation by Kalla et al. (1991) of the family of generalized radiation integrals defined by , where Re(γ) > Re(β) > 0; −1 < λ < 2 − 2μ > −1; μ > −1; p, a, b > 0; 0 < a b < ∞. Several recurr ence relations are presented. By differentiation of these integrals with respect to the parameters λ and μ we obtain also various integrals that include the logarithmic function in the integrand. Finally, we propose an algorithm for numerical evaluation of the generalized radiation integrals and illustrate it by tables of their values computed for selected values of the parameters. 相似文献
5.
Qing-Lun Wang Li-Na Zhu Dai-Zheng Liao Shi-Ping Yan Zong-Hui Jiang Peng Cheng Guang-Ming Yang 《Journal of Molecular Structure》2005,754(1-3):10-15
A new oxamato-bridged NiIICuIINiII species, [Ni(tacn)(H2O)]2[μ-Cu(pba)](ClO4)2·6H2O 1, (tacn=1,4,7-triazacyclononane; pba=1,3-propylenebis(oxamato)) has been synthesized and structurally as well as magnetically characterized. Complex 1 has a discrete trinuclear NiIICuIINiII structure: Two nickel(II) ions are bridged by [Cu(pba)]2− anion, macrocyclic ligand tacn works as terminal ligand of the nickel(II) center. The magnetic data of compound 1 was analyzed by means ofleading to gCu=2.19, gNi=2.18, J=−112.8 cm−1, D=±4.31 cm−1. The parameters are compared with the similar complexes and the irregular spin state structure of complex 1 is also described here. 相似文献
6.
Fabio E. Malanca M. Burgos Paci Gustavo A. Argüello 《Journal of photochemistry and photobiology. A, Chemistry》2002,150(1-3):1-6
Photolyses of CF3C(O)X and C2F5C(O)X (X=Cl, F) at 254 nm in the presence of O2 yield the perfluorinated radicals C2F5O (C2) and CF3O (C1), respectively. The C2 radicals decompose to give CF3 radicals:which, in turn, react with O2 leading to the formation of C1 radicals. When in addition to O2, CO is present, the C1 radicals react with it leading to its catalytic oxidation to CO2. The trioxide CF3OC(O)O3C(O)OCF3 was observed following the photolysis of all four halides in the presence of O2 and CO.
C2F5O→CF3+CF2O
The other radical partners coming from the initial step in the photolysis (XC(O)) as well as the products of their reaction with O2 (XC(O)Oy, y=1, 2) do not react with CO but when X=F they lead to the formation of a new stable peroxy molecule with the formula CF3OC(O)O2C(O)F. Some of the properties of this new molecule, its stability and its IR features are presented in this work. 相似文献
7.
A novel flow-injection system is proposed for the rapid measurement of the fish freshness indices K1 and K2: K1=[([HxR+[Hx])×100/([IMP]+[HxR]+[Hx])] and K2=[[Hx]×100/([HxR]+[Hx])], where [IMP], [HxR] and [Hx] are inosine-5′-monophosphate, inosine and hypoxanthine concentrations, respectively. For the estimation of index K1, 5′-nucleotidase immobilized reactor and nucleoside phosphorylase (NP)/xanthine oxidase (XO) coimmobilized reactor were incorporated in series in the flow-injection line made up by a 16-way switching valve with two sample loops. For the estimation of index K2, NP and XO immobilized reactors were also incorporated in the similar flow-line. Two sample portions passed through the flow-line with different residence times so that two peaks were obtained. The first and second peaks obtained in the K1-determining system corresponded to the total of HxR and Hx and the total of Hx, HxR and IMP, respectively. Similarly, the first and second peaks obtained in the K2-determining system corresponded to Hx and the total of Hx and HxR, respectively. Therefore, the indices K1 and K2 can be estimated by where i1 and i2 present the peak current of the first and second peaks, respectively, and f the ratio of the peak currents of the first and second peaks for a Hx standard solution. A sea bream was selected as a model fish and it was stored at 4 °C after death. A good correlation was found between the index K1 and the storage time over a period of 400 h, with a correlation coefficient of 0.992, but no correlation between the index K2 and the storage time. The measurements could be performed at a rate of 22 samples per hour with satisfactory precision (0.6–1.2% R.S.D.), without calibration for each species, accurate weighing of fish meat and any interferences in fish meat. 相似文献
8.
《Fluid Phase Equilibria》2005,233(1):86-95
In light of the available experimental data and of our current understanding of liquid–vapor critical phenomena, we examine the values of the parachors and of the parachor exponent, which are commonly used to estimate surface tension from the density difference between coexisting liquid and vapor phases. This is a controversial issue, as values for the parachor exponent ranging from 3.5 to 4 have been proposed in the literature. The parachor exponent and parachors can be viewed as a critical exponent and critical amplitudes, respectively. The Ising value, equal to 3.88, should be observed for the exponent “close enough” to the liquid/vapor critical point, i.e., for “low enough” tensions and densities. However, a review of experimental data for several fluids suggests an effective value in the range of 3.6, in line with the effective values observed for the exponents that describe the vanishing of the density difference and capillary length with the distance to the critical temperature. In fact, the asymptotic Ising regime is not reached experimentally, as confirmed by an estimation of the parachors very near the critical point. Those (Ising) parachors can be inferred from other critical amplitudes corresponding to bulk properties by using two-scale factor universality. Their values exceed those deduced from off-critical tension and density data by more than 10%, corresponding to surface tension differences larger than 50%. We argue that effective parachors (i.e., corresponding to an exponent in the range of 3.6) can be utilized in combination with two-scale-factor universality for determining the critical behavior of fluid systems in an extended range around their liquid/vapor critical point. 相似文献
9.
John K. Hogg Stuart L. James A. Guy Orpen Paul G. Pringle 《Journal of organometallic chemistry》1994,480(1-2):C1-C3
The metallo-phosphaalkenes (η5-C5Me5)(CO)2FeP=C(R)(SiMe3) (Ia: R = SiMe3, Ib: R = Ph) and MeO2C---CC---CO2Me undergo a dipolar [3+2]-cycloaddition to afford the metallo-heterocycles [(η5-C5Me5)(CO)=C(R)SiMe3] (IIIa,b) with exocyclic P=C double bonds. 相似文献
10.
Martina Dotzler Astrid Schmidt Jochen Ellermann Falk A. Knoch Matthias Moll Walter Bauer 《Polyhedron》1996,15(24):4425-4433
BiBr3 or SbI3 react at 20°C with LiN(PPh2)2 (1) to give elementary Bi or Sb and the P---P coupled phosphazene ligand Ph2P---N=PPh2---PPh2=N---PPh2 (2). The reaction of AsI3 with 1 at room temperature formed yellow needles of the eight-membered heterocycle
(3), whereas AsI3 interacted at 80°C with 1 in the molar ratio of 1:3 to give elementary arsenic and 2. Treatment of AsI3 and 1 at 20°C in a 1:2 stoichiometry yielded the seven-membered, cyclic arsenium(I) salt I·4THF (5·4THF), which was characterized by elemental analysis, conductivity, mass, IR and NMR spectroscopy and single-crystal X-ray structural analysis. 相似文献
11.
Pseudostate decomposition of static dipole polarizabilities for ground state H2+ from a Givens-Householder diagonalization of the excitation operator (H" height="17" width="20">0−E0) over an N-term basis of appropriate symmetry allows for a rapidly convergent evaluation of C6 dispersion coefficients for H2+–H2+. 27-term pseudospectra of hypergeneralized James functions with a 30-term GGJ+ unperturbed wavefunction with an optimized scale factor δ=0.918 at R=20 give C6 and γ6 values that are accurate to no less than nine significant figures. 相似文献
12.
Michael J. Chetcuti Phillip E. Fanwick Brian E. Grant 《Journal of organometallic chemistry》2001,630(2):215-220
The diketone complex [W(CO)2(η-C5H4Me){η3-(H)---C(O)---C5Me5}] (3) was isolated from the reaction of PhC2H with a mixture of [Ni(CO)I(η-C5Me5)] and [W(CO)3(η-C5H4Me)]−. Complex 3 contains an organic diketone fragment that is bound in a π-allyl fashion to a tungsten atom. It was fully characterized by standard spectroscopic techniques and by a single-crystal X-ray diffraction study. The relationship of complex 3 to a structurally characterized cyclopentadienyl tungsten η2-ketone species 1, and the likelihood that 3 and the methylcyclopentadienyl analog of 1 share common intermediates, are discussed. 相似文献
13.
Cline Schneider Frdric Doucet Stanislav Strekopytov Christopher Exley 《Polyhedron》2004,23(18):3185-3191
Hydroxyaluminosilicates (HAS) are critical secondary mineral phases in the biogeochemical cycle of aluminium. They are formed from the reaction of silicic acid (Si(OH)4) with an aluminium hydroxide template and act as a geochemical control of the biological availability of Al. There are two main forms of HAS which we have called HASA and HASB and which of these will predominate will depend upon the Si(OH)4 to Al ratio in any one environment. In all but the most heavily weathered environments or those undergoing a progressive acidification Si(OH)4 will be present in significant excess to Al and HASB will be the dominant secondary mineral phase. We have tried to determine the solubility of HASB(s) so that its contribution to Al solubility control might be compared with other secondary minerals such as Al(OH)3(gibbsite). In preliminary experiments, the dissolution of HASB(s) was found to be non-congruent with almost no Al being released during 18 months ageing. We then demonstrated that HASB(s) was significantly less soluble than Al(OH)3(s) prepared under identical experimental conditions. We have used this information to describe a solubility expression for HASB(s) at a predefined quasi-equibrium and to calculate a solubility constant.
K*Al2Si2O5(OH)4=[Al2O4+][SiO2]2[OH-]4