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1.
采用程序升温还原技术,在SO2存在气氛下,对钠、钙、铁及其复合物的NO-半焦催化反应性能进行了研究。结果表明,在相同条件下三种金属对NO-半焦反应的催化活性顺序为:Fe>Ca>Na。SO2可能通过参与氧传递过程来影响金属对NO-半焦反应的催化活性。SO2的浓度对负载三种不同金属半焦催化活性的影响是不同的。SO2浓度对负载钠半焦的催化活性影响最为显著。在SO2存在气氛下,负载2%钠或铁和负载3%钙的半焦具有高的NO转化活性。在SO2存在气氛下,钠-钙和钠-铁二元金属复合催化剂的活性较高,这可能是由于这两种金属间存在协同作用的缘故。 相似文献
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Silver colloid nanoparticles: synthesis, characterization, and their antibacterial activity 总被引:4,自引:0,他引:4
Panacek A Kvítek L Prucek R Kolar M Vecerova R Pizúrova N Sharma VK Nevecna T Zboril R 《The journal of physical chemistry. B》2006,110(33):16248-16253
A one-step simple synthesis of silver colloid nanoparticles with controllable sizes is presented. In this synthesis, reduction of [Ag(NH(3))(2)](+) complex cation by four saccharides was performed. Four saccharides were used: two monosaccharides (glucose and galactose) and two disaccharides (maltose and lactose). The syntheses performed at various ammonia concentrations (0.005-0.20 mol L(-1)) and pH conditions (11.5-13.0) produced a wide range of particle sizes (25-450 nm) with narrow size distributions, especially at the lowest ammonia concentrations. The average size, size distribution, morphology, and structure of particles were determined by dynamic light scattering (DLS), transmission electron microscopy (TEM), and UV/Visible absorption spectrophotometry. The influence of the saccharide structure (monosacharides versus disaccharides) on the size of silver particles is briefly discussed. The reduction of [Ag(NH(3))(2)](+) by maltose produced silver particles with a narrow size distribution with an average size of 25 nm, which showed high antimicrobial and bactericidal activity against Gram-positive and Gram-negative bacteria, including highly multiresistant strains such as methicillin-resistant Staphylococcus aureus. Antibacterial activity of silver nanoparticles was found to be dependent on the size of silver particles. A very low concentration of silver (as low as 1.69 mug/mL Ag) gave antibacterial performance. 相似文献
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Yu-Nung Su Ming-Sung Tsai San-Yan Chu 《International journal of quantum chemistry》1996,59(6):487-493
We performed ab initio calculations for protonated P2, N2, NP, and their isoelectronic species, i.e., CO, CS, SiO, and SiS. The proton affinities at different sites were examined to characterize special properties of the second-row elements. To tune the acid strength, we also studied the Li+ and Na+ affinities for comparison. These systems are isovalent to acetylene and disilyne; their structural features such as linear or bent is of special interest. All calculations were performed by the GAUSSIAN 92 program using the 6-31G** basis set and the basis set at the Hartree-Fock and MP2(full) levels. Bent structures were found for XP+2, CSH+, and SiSX (X = H+, Li+, Na+). © 1996 John Wiley & Sons, Inc. 相似文献
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Summary The relative importance of the valencep functions for describing the bonding in the valence isoelectronic Na2, K2, and Cu2 molecules and their positive and negative ions is investigated. In absolute magnitude the contribution of thep functions to the dissociation energy follows the trend Cu>Na>K while by percentage of the dissociation energy the importance of thep functions follows the polarizabilities, i.e. K>Na>Cu. The bonding in K2, K
2
+
, and K
2
–
is analyzed to explain the observed trends.Dedicated to Prof. Klaus Ruedenberg 相似文献
6.
X-ray diffuse scattering has been measured by single-crystal X-ray diffraction on the lead-free piezoelectric perovskites Na0.5Bi0.5TiO3 (NBT) and (Na0.5Bi0.5)0.89Ba0.11TiO3 (NBT–Ba0.11). Evidence of a pronounced local structure or included phase different from the rhombohedral average symmetry (space group R3c), or of a modulated structure with a characteristic period of 40 Å, is presented for NBT from high-resolution synchrotron X-ray mapping and CCD diffractometer investigations. The additional scattering shows pronounced anisotropy and produces satellite peaks displaced by 0.2 in the h and k indices for reflections such as {640} indexed on the pseudo-cubic unit cell with a = 7.761(2) Å. By contrast, weaker, less anisotropic diffuse scattering is observed for tetragonal NBT–Ba0.11 (space group P4mm), which is directed along the pseudo-cubic 〈110〉. The lack of satellite peaks and pronounced anisotropic diffuse scattering in the tetragonal phase of phase NBT–Ba0.11 lends support to the idea that the massive tetragonal to rhombohedral phase transition in NBT at around 503–573 K, which is absent in NBT–Ba0.11, may be the key to understanding the local structure found repeatedly at room temperature in this complex material. 相似文献
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We report the separate and combined effects of humic acid and Ca2+ ions on the transport of colloidal particles through a sand-packed column. Polystyrene latex particles with a sulfate functional
group were used as model colloids. The concentrations of both the inlet solution and the effluent solutions were measured
during each experimental run. Breakthrough curves were obtained by taking the ratios of each effluent sample concentration
to the inlet solution concentration. In the absence of humic acid, the results indicate that increasing the concentration
of Ca2+ increases particle attachment to the sand, thus causing decreased transport rates of latex particles through the porous bed
matrix. Once 4 mg/l humic acid was added to the system, changes were observed in the effect that Ca2+ has on latex particle breakthrough. In a system containing calcium, increasing the humic acid concentration was shown to reduce
particle attachment and increase transport rates. In the absence of calcium, the ratios for the outlet-to-inlet concentrations
were similar for each concentration of humic acid. The electrophoretic mobility was also measured in order to determine the
role of electrostatic repulsion in the latex particle transport. The electrophoretic mobility of the latex particles was found
to be dependent on humic acid concentration in the absence of Ca2+ but not in its presence.
Received: 2 February 2001 Accepted: 6 2001 相似文献
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The doubly excited valence (3p+3p) 2 (1)Delta(g) state of Na(2) is experimentally observed by using optical-optical double resonance spectroscopy. A single line Ar(+) laser (a total of nine lines) was used to pump the sodium dimers from thermally populated ground state X (1)Sigma(g) (+) to the intermediate B (1)Pi(u) state. Then, a single mode Ti:sapphire laser was used to probe the doubly excited 2 (1)Delta(g) state. Violet fluorescence emitted from the highly excited states (mainly 2 (3)Pi(g) or 3 (3)Pi(g) states which are transferred from 2 (1)Delta(g) state via collision) to the a (3)Sigma(u) (+) state was monitored by a filtered photomultiplier tube (PMT). A total of 582 rovibrational levels of 2 (1)Delta(g) state were observed, identified, and assigned to the vibrational and rotational quantum numbers in the range of 0< or =v< or =28 and 11< or =J< or =99, respectively. The absolute vibrational quantum number assignment was verified by comparing the totally resolved fluorescence with the calculated Franck-Condon factors between 2 (1)Delta(g) state and B (1)Pi(u) state. Dunham coefficients and Rydberg-Klein-Rees potential curve were derived from these observed quantum levels. The primary molecular constants of Na(2) 2 (1)Delta(g) state are T(e)=32 416.759(15) cm(-1), omega(e)=124.8484(36) cm(-1), B(e)=0.119 158(3) cm(-1), and R(e)=3.508 20(5) A. 相似文献
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用改进硬脂酸溶胶-凝胶法制备了量子顺电体La1/2Na1/2TiO3纳米晶,用差热-热重分析和X射线衍射测试了样品的晶化过程及物相结构,用FTIR和Raman光谱表征了其谱学特性. 相似文献
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Ensemble total internal reflection microscopy is used to measure reversible temperature- and specific-ion-mediated interaction potentials between macromolecule-coated colloids and surfaces. Potentials are measured between PEO-PPO-PEO (poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide)) block copolymers adsorbed to hydrophobically modified silica colloids and glass or gold planar surfaces. Conditions investigated include temperatures from 20 to 47 degrees C and MgSO4 concentrations from 0.2 to 0.5 M. The solvent-quality-mediated copolymer layer collapse inferred by comparing measured potentials and the predicted van der Waals attraction, including effects of the adsorbed copolymer and surface roughness, displays good agreement with expected limits based on the PEO block contour length and the bulk PEO density. Superposition of all PEO layer collapse measurements onto a single universal curve, via a transformed temperature scale relative to a reference temperature in each case, indicates an equivalence of increasing temperature and increasing MgSO4 concentration when layer interactions and dimensions are mediated. Accurate knowledge of nanometer- and kT-scale interactions of copolymer-coated colloids as a function of temperature and MgSO4 concentration provides the ability to reversibly control the stability, phase behavior, and self-assembly of such particles. 相似文献
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James F. Harrison Daniel B. Lawson 《International journal of quantum chemistry》2005,102(6):1087-1091
The quadrupole moments (Θ) of Li2, Na2, and K2 have been determined using SCF, B3LYP, and CCSD(T). Included in this study is the effect of valence and core–valence correlation. The variation of Θ as a function of bond length has also been evaluated from which vibrational contributions have been determined. Additionally, the shape and relative magnitude of Θ vs. bond length are attributed to the s–s nature of the bonding. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2005 相似文献
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1, 2-Diazabicyclo [2.2.2] octane, its 6-methyl homolog, and 1, 2-diazabicyclo [3.2.1] octane are synthesized by a general method involving nitrosation of piperidine carboxylic acids, subsequent reduction to 1-aminopiperidine carboxylic acids, cyclization to 3-keto-1, 2-diazabicycloalkanes, reduction of the latter to 1, 2-diazabicycloalkanes. A number of 2-substituted 1, 2-diazabicyclo [2.2.2] octanes are synthesized. 相似文献
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Na2MnO2 was prepared via the azide/nitrate route. Stoichiometric mixtures of the precursors (Mn2O3, NaN3 and NaNO3) were heated in an appropriate regime up to 390 °C and annealed at this temperature for 20 h, in specially designed silver containers. As the most prominent feature, the crystal structure of Na2MnO2 (C2/c, Z = 12, a = 12.5026(9), b = 12.1006(9), c = 6.0939(4) Å, β = 117.94(0)°, 1556 independent reflections, R1 = 3.83 % (all data)) forms a three dimensional framework polyanion of corner sharing MnO4‐tetrahedra. The connectivity pattern of the tetrahedral building units corresponds to the moganite structure, a rare SiO2 modification. According to measurements of the magnetic susceptibility in the temperature range from 2 to 750 K, Na2MnO2 shows antiferromagnetic ordering below 250 K. Evaluation of the high temperature data employing the Curie‐Weiss law revealed a magnetic moment of μeff = 5.93 μB, confirming the presence of divalent manganese. 相似文献
14.
M. A. Rekhter 《Chemistry of Heterocyclic Compounds》1996,32(4):408-417
2-Acylindoles and 2-acylindole-3-carboxylic acids are readily alkylated at the nitrogen atom by haloalkanes in a superbasic medium (DMSO + NaOH). For the carboxylic acids, this reaction may proceed either entirely at the nitrogen atom, or at both the the nitrogen atom and the carboxyl group, depending on the content of water in the medium and the alkali -haloalkane ratio.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 472–482, April, 1996. 相似文献
15.
Jones AR Winter R Greaves GN Smith IH 《The journal of physical chemistry. B》2005,109(49):23154-23161
The glass-forming reactions between sodium carbonate (Na2CO3) and silica (SiO2) have been investigated by 23Na, 29Si, and 13C magic-angle spinning (MAS) NMR spectroscopy. The multinuclear MAS NMR approach identifies and quantifies reaction products and intermediates, both glassy and crystalline. A series of powdered batches of initial composition Na2CO3.xSiO2 (x = 1, 2) corresponding to a sodium metasilicate (Na2SiO3) and sodium disilicate (Na2Si2O5) stoichiometry were investigated after periods of isothermal and nonisothermal heat treatments at different temperatures. Analysis of the 23Na quadrupolar coupling parameters has identified the early reaction product in all cases as crystalline Na2SiO3. In the nonisothermal experiment, this reaction is preceded by an early silica-rich melt phase formed around 850 degrees C. The early reactions are controlled by solid-state Na+ diffusion across the reaction zone in the grain interface layer. Crystalline Na2SiO3 precipitates in the interface layer, increasing its thickness between the Na2CO3 and the SiO2 grains and slowing down the rate of Na+ migration. This creates a secondary phase, which is temperature dependent. At low temperatures, where Na+ migration is impaired, the production of Na2SiO3 ceases and silica-richer phases are precipitated. In the case of the sodium disilicate batch, where excess SiO2 is present, a secondary reaction of Na2SiO3 with SiO2 forming a glassy phase is observed. A transient carbon-bearing phase has been identified by 13C NMR as a NaCO3- complex loosely bound to bridging oxygens in the silicate network at the SiO2 grain surface. 相似文献
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Y H Zhang D M Chen T He F C Liu 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2001,57(13):2599-2605
This paper reports a novel reaction of metallotetraphenylporphyrins on hydroxyl-modified silver colloid and Ag2O colloid. Surface-enhanced Raman spectra of Ag(II) and Cu(II) complexes of tetraphenylporphyrin (TPP) adsorbed on the hydroxyl-modified Ag colloid and Ag2O colloid have been studied. The time-dependent SERS spectra of MTPP (M = Ag, Cu) on hydroxyl-modified Ag colloid were recorded and dramatic change on SERS spectra was observed. The final spectra were found to be strikingly different from the corresponding normal Raman spectra (NRS), with the appearance of new Raman bands at 1614. 1417, 947, 674 and 292 cm(-1). The UV-visible absorption spectrum of MTPP on hydroxyl-modified Ag colloid exhibits a broad shoulder near 460 nm. Similar spectral phenomena were also observed for AgTPP and CuTPP adsorbed on Ag2O colloid. The observed spectral alterations were ascribed to new species formation due to the irreducible oxidation of MTPP on the colloids. 相似文献
20.
Milan Potá?ek Alois Kuka?ka Milo? Petr? Amalia Manolopulu Josef Havel 《Reaction Kinetics and Catalysis Letters》1993,51(1):135-141
6-Substituted 2-(2-benzothiazolyl) [1, 2, 3] benzotriazol-1-oxides were prepared by a base catalyzed cyclization reaction of 2-(4-substituted 2-nitrophenylhydrazino) benzothiazoles. Influence of substitution in position 4 on the cyclization reaction rate was followed and correlated with Hammett constants. 相似文献