共查询到20条相似文献,搜索用时 23 毫秒
1.
M. M. Kasumov 《Technical Physics Letters》2010,36(10):895-898
The mass spectrum of the products of arc discharge in helium between graphite electrodes has been studied for various values
of the gas flow rate. As the gas flow rate increases, the intensity of C60±, C70±, C84± and C90± fullerene peaks increases and that of the C2− and C3+ cluster radicals decreases, but the total decay in radicals amounts to only 21% of the total growth of fullerenes. From this
it follows that a contribution to the formation of fullerenes from the neutral clusters (which are taken into account for
the first time) significantly exceeds the contribution due to small radical species. 相似文献
2.
O. D. Maslov G. A. Bozhikov P. I. Ivanov M. V. Gustova A. G. Belov S. N. Dmitriev 《Radiochemistry》2010,52(1):87-89
237U was produced by the reaction 238U(γ, n) on an electron accelerator, MT-25 microtron, at the Flerov Laboratory of Nuclear Reactions. For the separation of 237U and [238U, the recoil nuclei were collected by a nanostructured material, hydrated manganese dioxide (of the cryptomelane type), in
the solid-solid system. From fission products, 237U was separated by ion exchange. The specific activity of the resulting 237U was 4.5 × 109 Bq (mg 238U)-1, with the content of radioactive impurities of ≤10-6 Bq Bq-1. The chemical yield of 237U was 80%. 相似文献
3.
Boyd D Towler MR Wren A Clarkin OM 《Journal of materials science. Materials in medicine》2008,19(4):1745-1752
Conventional polymethylmethacrylate (PMMA) cements and more recently Bisphenol-a-glycidyl dimethacrylate (BIS-GMA) composite cements are employed in procedures such as vertebroplasty. Unfortunately, such materials have inherent drawbacks including, a high curing exotherm, the incorporation of toxic components in their formulations, and critically, exhibit a modulus mismatch between cement and bone. The literature suggests that aluminium free, zinc based glass polyalkenoate cements (Zn-GPC) may be suitable alternative materials for consideration in such applications as vertebroplasty. This paper, examines one formulation of Zn-GPC and compares its strengths, modulus, and biocompatibility with three commercially available bone cements, Spineplex, Simplex P and Cortoss. The setting times indicate that the current formulation of Zn-GPC sets in a time unsuitable for clinical deployment. However during setting, the peak exotherm was recorded to be 33 degrees C, the lowest of all cements examined, and well below the threshold level for tissue necrosis to occur. The data obtained from mechanical testing shows the Zn-GPC has strengths of 63 MPa in compression and 30 MPa in biaxial flexure. Importantly these strengths remain stable with maturation; similar long term stability was exhibited by both Spineplex and Simplex P. Conversely, the strengths of Cortoss were observed to rapidly diminish with time, a cause for clinical concern. In addition to strengths, the modulus of each material was determined. Only the Zn-GPC exhibited a modulus similar to vertebral trabecular bone, with all commercial materials exhibiting excessively high moduli. Such data indicates that the use of Zn-GPC may reduce adjacent fractures. The final investigation used the well established simulated body fluid (SBF) method to examine the ability of each material to bond with bone. The results indicate that the Zn-GPC is capable of producing a bone like apatite layer at its surface within 24 h which increased in coverage and density up to 7 days. Conversely, Spineplex, and Simplex P exhibit no apatite layer formation, while Cortoss exhibits only minimal formation of an apatite layer after 7 days incubation in SBF. This paper shows that Zn-GPC, with optimised setting times, are suitable candidate materials for further development as bone cements. 相似文献
4.
The enthalpy stability of the LaCl 4 ? and LuCl 4 ? ions is assessed using high-temperature mass spectrometry. The enthalpy of Cl? detachment is determined to be ΔrH0(298.15 K) = 332 ± 10 kJ/mol for LaCl 4 ? and 359 ± 10 kJ/mol for LuCl 4 ? . 相似文献
5.
O. P. Krivoruchko T. V. Larina V. F. Anufrienko I. Yu. Molina E. A. Paukshtis 《Inorganic Materials》2009,45(12):1355-1361
We have synthesized nanoparticulate cobalt(II) hydroxide containing Co2+ in tetrahedral oxygen coordination (Co Td 2+ ), atypical of such systems: nano- [Co(OH)2(H3O) δ + ]δ+. The (Co Td 2+ ) coordination in the hydroxide is inferred from its electronic diffuse reflectance spectrum, which shows a multiplet of strong absorption bands at 14500, 15000, and 16000 cm?1 (4 A 2(F)-4 T 1(P) transition). Nanoparticulate cobalt(II) hydroxide forms in a weakly acidic medium under essentially nonequilibrium conditions due to supersaturation (by three to four orders of magnitude) with the starting reagents (CoCl2 and LiOH) at the instant of the formation of the poorly soluble phase Co(OH)2. Presumably, colloidal particles of nanoparticulate cobalt(II) hydroxide in a weakly acidic aqueous medium have a positive surface charge, compensated by a counter-ion (Cl?) layer: nano-[Co(OH)2(H3O) δ + ]δ+ · δCl?. The XRD patterns of pastes (gels) containing this hydroxide show three broad-ened lines with d = 5.31 (2θ = 16.7°), 2.77 (2θ = 32.3°), and 2.32 Å (2θ = 38.8°). According to small-angle X-ray scattering data, nano-[Co(OH)2(H3O) δ + ]δ+ has a narrow particle size distribution (1.0–2.0 nm). Synthesis and storage conditions are identified which ensure stabilization of the electronic state and particle size of nano-[Co(OH)2(H3O) δ + ]δ+ for a long time. 相似文献
6.
S. Y. Lee Y. L. Lu P. K. Liaw H. Choo S. A. Thompson J. W. Blust P. F. Browning A. K. Bhattacharya J. M. Aurrecoechea D. L. Klarstrom 《Mechanics of Time-Dependent Materials》2008,12(1):31-44
The creep–fatigue crack-growth tests of HASTELLOY® X alloy were carried out at the temperatures of 649°C, 816°C, and 927°C in laboratory air. The experiments were conducted under a constant stress-intensity-factor-range (ΔK) control mode with a R-ratio of 0.05. In the constant ΔK tests, a ΔK of 27.5 MPa\(\sqrt{\mathrm{m}}\) and a triangular waveform with a frequency of 0.333 Hz were used. Various tensile hold times at the maximum load were imposed to study fatigue and creep–fatigue interactions. Crack lengths were measured by a direct current potential drop method. In this paper, effects of hold time and temperature on the crack-growth rates are discussed. Furthermore, the crack-growth rates of the HASTELLOY® X alloy are compared to those of the HAYNES® 188 and HAYNES® 230® superalloys. 相似文献
7.
E. Ricci D. Giuranno R. Novakovic T. Matsushita S. Seetharaman R. Brooks L. A. Chapman P. N. Quested 《International Journal of Thermophysics》2007,28(4):1304-1321
The surface tension, density, and viscosity of the Ni-based superalloy CMSX-4® have been determined in the temperature ranges of 1,650–1,850 K, 1,650–1,950 K, and 1,623–1,800 K, respectively. Each property has been measured in parallel by different techniques at different participating laboratories, and the results are compared with the aim to improve the reliability of data and to identify recommended values. The following relationships have been proposed: density-ρ (T) [kg· m?3] = 7,876 ? 1.23(T ? 1,654 K); surface tension-γ (T) [mN·m?1] = 1,773 ? 0.56 (T ? 1, 654 K); viscosity-η (T) [mPa·s] = 8.36 ? 1.82 × 10?2(T ? 1,654 K). For a comparison, surface-tension measurements on the Al-88.6 at% Ni liquid alloy with the same Al-content as the CMSX-4® alloy were also performed. In addition, the surface tension and density have been theoretically evaluated by different models, and subsequently compared with new experimental data as well as with those reported in the literature. The surface-tension experimental data for the liquid CMSX-4® alloy were found to be close to that of the Al-88.6 at% Ni alloy which is consistent with results from the compound formation model (CFM). 相似文献
8.
A. S. Bolonkin 《Radiochemistry》2010,52(5):455-461
Results of experiments on determination of the energy of 213Bi α-particles for the existing lines with the intensities of 1.94 and 0.15% per decay are reported. The results were obtained
by semiconductor α-ray spectrometry by comparison with the α-particle energies for the major lines of 221Fr and 213Po, known with a lower uncertainty. The experiments were designed so as to minimize and, at the same time, take into account
factors affecting the deviations of the peak maxima from the true values. Special emphasis is made on the decay of recoil
nuclei on the detector surface. To eliminate this effect, samples containing highly nonequilibrium systems 213Bi + 221Fr and 213Bi + 225Ac were prepared. For the measurement conditions used, the equilibrium spectra of 225Ac with daughter decay products were found to be unsuitable for accurate determination of the energy of the 213Bi major peak and can be used only for tentative estimations. The actual energies of 213Bi α-radiation do not coincide with the assessed reference data used today and are in the region of the upper limit of the
uncertainty range for these data. The results show that the presently used energy characteristics of 213Bi α-radiation require refinement. 相似文献
9.
Synthesis of free standing conducting polypyrrole film using room temperature melt as the electrolyte is reported. We also report variation in the contribution of ionic conductance with temperature of the polymer film by four probe method and electrochemical properties like diffusion coefficient and ionic mobility of AlCl−4 doped polypyrrole film. An attempt has been made to arrive at the stability of charge carrier concentration over a temperature range of 295 to 350 K under vacuum. The film was characterized by optical techniques and scanning electron micrography. 相似文献
10.
Tomohito Kameda Toshiaki Yoshioka Fumiko Yabuuchi Miho Uchida Akitsugu Okuwaki 《Bulletin of Materials Science》2008,31(4):625-629
In this study, we confirmed that the characteristics of anion intercalation into the interlayer of a hydrotalcite-like compound
(HT) during synthesis are similar to those of the anion-exchange reaction of HTs as well as the reconstruction reaction of
HTs from Mg-Al oxide. We demonstrated that (i) Cl−, which has a higher charge density than NO3−, more easily reacted with Mg and Al species to form HT structure, resulting in greater intercalation of Cl− into the HT interlayer; and (ii) for HTs with lower Mg: Al molar ratios, OH−, which has a higher charge density than Cl− and NO3−, was more likely to interact with Mg and Al species to form HT structure, blocking the intercalation of Cl− and NO3−. Furthermore, we showed that high concentrations of Cl− and NO3− in solution regulated their intercalation into the HT interlayer. The high activity of Cl− and NO3− in solution would facilitate the anions’ reactions with Mg and Al species to form HTs, resulting in a high degree of anion
intercalation into the interlayer of HTs. 相似文献
11.
Yanbo Qiao Ning Da Danping Chen Wenbo Ma Qinling Zhou Jianrong Qiu 《Journal of Materials Science》2009,44(15):4026-4030
The Nd3+, Yb3+-doped and Nd3+–Yb3+-codoped high silica glasses (HSGs) were fabricated by sintering porous glasses impregnated with Nd3+ and Yb3+ ions solutions. The Judd–Ofelt theory was used to study the spectroscopic properties of Nd3+-doped HSGs. Large parameter Ω2 of Nd3+-doped HSGs suggests a lower centrosymmetric coordination environment around the Nd3+ in HSG. The spontaneous emission probability and emission cross-section (σem) of Yb3+-doped HSGs are obtained. A broad emission band from 950 to 1,100 nm was detected when the Nd3+–Yb3+-codoped HSG was excited by 808 nm LD. The energy transfer process from Nd3+ to Yb3+ in HSG was described in this paper. 相似文献
12.
Yu. A. Barbanel’ R. B. Dushin V. V. Kolin V. P. Kotlin L. G. Mashirov S. N. Nekhoroshkov 《Radiochemistry》2007,49(3):237-240
The absorption spectra of the NpO 2 + (5f 2) ion were examined in the region of the 3H 5 ← 3 H 4 magnetic dipole transition (1530–1760 nm) for series of melts with the UO 2 2+ concentration varied in the opposite directions: (1) NaCl-2CsCl eutectic melt with growing additions of the Cs2UO2Cl4 complex salt and (2) Cs2UO2Cl4 melt with growing additions of the NaCl-2CsCl mixture. Measurements of the integrated intensities of the bands belonging to the NpO 2 + ·UO 2 2+ complex and unbound NpO 2 + throughout the UO 2 2+ concentration range examined (up to 4.4 M in neat Cs2UO2Cl4 melt) and processing of the data obtained in terms of the mass action law showed that the formation-decomposition reaction of the cation-cation complex can be described adequately only using the equation of reaction in the form NpO2Cl 4 3? + UO2Cl 4 2? ? {Cl4ONpO?UO2Cl3}4? = Cl? (with the equilibrium constant of 1.3±0.1). Thus, the formation of the cationcation complex should be treated as replacement of chloride ion in the equatorial plane of uranyl(VI) by neptunyl(V), rather than as simple addition of UO 2 2+ to NpO 2 + . The reverse reaction, decomposition of the cation-cation complex, consists essentially in replacement of neptunyl(V) by chloride ion. 相似文献
13.
Compounds CsAVA′VIO6 (AV = Sb, Ta; A′VI = W, U) were synthesized by high-temperature solidphase reactions. The crystal structures of the compounds were refined by the Rietveld method (space group Fd \(\bar 3\) m). 相似文献
14.
Xing Gao Taiwen Li Jianfeng He Kexin Ye Xiaojiao Song Nengli Wang Jiangang Su Chunlong Hui Xiyan Zhang 《Journal of Materials Science: Materials in Electronics》2017,28(16):11644-11653
Well-crystalline β-NaYF4:Yb3+, Ho3+, Tm3+ nanoparticles were synthesized by sol–gel method using isopropyl alcohol [(CH3)2CHOH] as a complexing agent. The samples were characterized by X-ray diffraction, scanning electron microscopic analysis and fluorescence spectrum analysis methods. Under the excitation of 980 nm laser diode (LD), the samples displayed bright upconversion luminescence (UCL), which was generated from the energy level transition of Ho3+ and Tm3+ ions. With the increase of Tm3+, Ho3+ and Yb3+-doping concentration, the UCL intensity of blue, green and red light emission of the samples varied. Calculation of the CIE color coordinate of the β-NaYF4:Yb3+, Ho3+, Tm3+ nanoparticles revealed that with the adjustment of Tm3+, Ho3+ and Yb3+ doping concentration and the excitation power of 980 nm LD, the multi-color UCL can be realized. Approximately single red light output with the CIE color coordinate of x?=?0.545, y?=?0.306 and white light output with the CIE color coordinate of x?=?0.325, y?=?0.320 can be obtained in the synthesized β-NaYF4: Yb3+, Ho3+, Tm3+ nanoparticles. 相似文献
15.
O. V. Nipruk N. G. Chernorukov K. A. Chaplieva G. N. Chernorukov 《Inorganic Materials》2016,52(5):504-509
We have developed a process for the synthesis of Ni(II) and Zn(II) triuranates with the general formula MIIU3O10 · 6H2O through reaction of schoepite, UO3 · 2.25H2O, with aqueous solutions of nickel and zinc nitrates under hydrothermal conditions. Using chemical analysis, X-ray diffraction, IR spectroscopy, and thermal analysis, we have determined the composition and structure of the triuranates and investigated their dehydration and thermal decomposition. 相似文献
16.
A specific feature of U(IV) oxidation with xenon difluoride in aqueous H2SO4 solutions is low-temperature chemiluminescence (CL), which in the course of warming the sample quickly cooled to 77 K is recorded starting from 165 K and reaches a maximum at about 200 K. Exothermic phase transitions, crystallization of the ice + H2SO4·4H2O and ice + H2SO4·6.5H2O eutectics, occur in the same temperature range. The data (temperature dependences of the chemiluminescence intensity and simultaneously recorded DTA curves) obtained in experiments with variation of the rate of mixing and cooling the solutions and of the concentrations of H2SO4 and F? and UO 2 2+ ions are well explicable by the catalytic activity of the juvenile surface of H2SO4 crystal hydrates toward low-temperature reaction of U(IV) with XeF2. 相似文献
17.
In this paper, we report the synthesis of Ce3 + and Dy3 + activated alkali lanthanide tungstates, ALa(WO4)2(where A = Na and Li), prepared by solid state reaction method. The prepared phosphors were characterized by X-ray diffraction
and photoluminescence techniques. The NaLa(WO4)2:Dy3 + and LiLa(WO4)2:Dy3 + phosphors show two emission peaks at around 574 and 486 nm (λexc = 354 nm). NaLa(WO4)2:Ce3 + and LiLa(WO4)2:Ce3 + show two emission peaks at around 378 and 425 nm (λexc = 350 nm). Excitation wavelengths of Ce3 + and Dy3 + activated alkali lanthanide tungstates are in near UV region i.e. Hg free excitation. These characterizations of phosphors
are applicable for solid state lighting. Accordingly, Ce3 + and Dy3 + activated NaLa(WO4)2 and LiLa(WO4)2 may be the promising materials for solid state lighting applications. 相似文献
18.
Glasses of the 0.5Er3+/2.5Yb3+ co-doped (40Bi2O3–20GeO2–(30 − x)PbO–xZnO–10Na2O system where x = 0.0, 5, 10, 15, 20, 25, and 30 mol%) have been characterized by FT-IR spectroscopy measurements to obtain information about
the influence of ZnO-substituted PbO on the local structure of the glass matrix. The density and the molar volume have been
determined. The influences of the ZnO-substituted PbO on the structure of glasses have been discussed. The dc conductivity
measured in the temperature range 475–700 K obeys Arrhenius law. The conductivity decreases while the activation energy for
conduction increases with increase ZnO content. The optical transmittance and reflectance spectrum of the glasses have been
recorded in the wavelength range 400–1100 nm. The values of the optical band gap E
opt for all types of electronic transitions and refractive index have been determined and discussed. The real and imaginary parts
ε1 and ε2 of dielectric constant have been determined. 相似文献
19.
Distribution of 210Po in thalli of soil and wood (epiphytic) lichens was studied. Four fractions containing the corresponding 210Ро forms were obtained by sequential extraction: (1) intercellular, (2) extracellular, (3) intracellular, and (4) insoluble thallus residue. The 210Ро uptake by lichens is mainly passive, as the total content of the radionuclide in fractions 1, 2, and 4 reaches 88–97%. From 3 to 12% of 210Ро is taken up actively (fraction 3), and for soil lichens this parameter is approximately 2.75 times higher than for epiphytic lichens. Presumably, 210Ро is supplied into soil and epiphytic lichens in the form of different chemical compounds and is therefore characterized by different bioavailability. 相似文献
20.
The total stability constants of Th4+, U4+, Np4+, Pu4+, Am4+, Cm4+, Ce4+, Tb4+, Pr4+, Tb3+, and Pr3+ complexes with P2W17O 61 10? heteropolyanion in 1 M sodium salt solutions at pH ≥ 5.5 (i.e., when the anion is not protonated; so-called “absolute” constants), were determined experimentally or calculated from published data. Plots of constants vs. ionic radius of the f element were considered for solutions with ionic strength 1 (1 M acid or sodium salt solutions at pH ≥ 5.5). The correlations found confirm that the interaction of counterions in the complex is predominantly electrostatic. At the same time, different contributions of the covalent interaction for actinides and lanthanides were suggested. 相似文献