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991.
烟酸对酸性硫酸盐体系铜电沉积的影响 总被引:2,自引:0,他引:2
对溶液A: 0.8 mol•L-1硫酸铜,0.6 mol•L-1硫酸,5.0×10-5 mol•L-1氯离子,1.0×10-4 mol•L-1聚乙二醇的溶液,溶液B:在溶液A中加入2.0×10-2 mol•L-1烟酸,pH为0.5,运用循环伏安和计时安培法研究玻碳电极上铜的电沉积行为.结果表明,铜的电沉积过程经历了晶核形成过程,其电结晶按瞬时成核和三维生长方式进行.烟酸的加入对铜的电沉积具有阻化作用,但不改变铜的电结晶机理.沉积层的X射线衍射表明Cu为面心立方结构,在烟酸存在下沉积层出现(220)高择优取向,这可能是烟酸在Cu(220)晶面上发生强烈吸附作用的结果. 相似文献
992.
Residual stress in the epoxy plate during a rapid cooling process was measured by the layer removal method and calculated by the linear thermoviscoelastic theory considering specific volume relaxation. The relaxations of the tensile modulus and specific volume were measured by an Instron thermomechanical analyzer. When the starting temperature of the cooling process was near the glass transition temperature of the cured epoxy, the residual stress in the epoxy plate was smaller than when the starting temperature was higher than the glass transition temperature. However, the transient stress in the cured epoxy plate was higher when the starting temperature was near the glass transition temperature than when the starting temperature was higher than the glass transition temperature. The quenched epoxy plate was compressed in the direction parallel to the surface and expanded in the thickness direction. 相似文献
993.
The goal of this work was the development of a novel type of heterogeneous catalyst, consisting of bare metal nanoparticles
on stainless steel foils, which can be shaped to any kind of architecture and, if necessary, heated electrically. Solutions
of pre-prepared, ligand protected and monodispersed gold, palladium, platinum and rhodium nanoparticles were sprayed onto
stainless steel foils, followed by the careful removal of the ligand molecules by an oxygen plasma treatment. Due to this,
bare particles become irreversibly fixed on the steel support. It could be shown that the original particle sizes do not change
during the plasma treatment. Foils, densely coated with the nanoparticles, were used for gas phase catalyses in a self-made
reactor at room temperature or at 60 °C. Hydrogenation of 1,3-butadiene at 15 nm Pd and 2 nm Pt, CO oxidation at 16 nm, 8 nm
and 1.4 nm gold and NO reduction with NH3 at 2 nm Rh particles were performed, indicating that the novel catalysts might in principle be applicable in technical processes
if the experimental conditions like form and temperature would be optimized.
Dedicated to Professor Dieter Fenske on the occassion of his 65th birthday. 相似文献
994.
Xiao-Bai Sun Pei-Hua Zhao Yang-Jun Xu Li-Mei Sun Mei-Ai Cao Cheng-Shan Yuan 《Chemistry of Natural Compounds》2007,43(5):563-566
Investigation of the roots of Polygonum bistorta L. afforded seven compounds including five triterpenoids, a coumarin, and a steroid, the structures of which were identified
by EIMS, 1H NMR, 13C NMR, DEPT, and HMBC experiments. All the compounds have been isolated from Polygonum genus for the first time.
Published in Khimiya Prirodnykh Soedinenii, No. 5, pp. 463–465, September–October, 2007. 相似文献
995.
A new Schiff base has been synthesized from 4-aminoantipyrine and 3-formylsalicylic acid. The ligand has a dianionic tetradentate compartmental OONO donor system. The cobalt(II), nickel(II), copper(II) and dioxouranium(VI) complexes exist in phenolato-bridged dinuclear species, while palladium(II) gives a mononuclear complex with free –COOH groups. The complexes have been characterized by elemental analyses, i.r., u.v.-vis, thermal and magnetic measurements. 相似文献
996.
Wanxing Wei Yuanjiang Pan Yaozu Chen Cuiwu Lin Tengyou Wei Shukai Zhao 《Chemistry of Natural Compounds》2005,41(1):17-21
Five compounds, terephthalic acid mono-[2-(4-carboxy-phenoxycarbonyl)-vinyl] ester (1), (E)-3-(5′-hydroperoxy-2,2′-dihydroxy[1,1′-biphenyl]-4-yl)-2-propenoic acid (2), 3,4,5-trihydroxybenzoic acid (3), succinic acid (or butanedioic acid) (4), and 2,3,4,5,6-pentahydroxybenzoic acid (5), were isolated from Phyllanthus urinaria. The structures of these compounds were elucidated by means of spectral techniques including IR, MS, and 1D/2D NMR. 1 and 2 are new compounds.__________Published in Khimiya Prirodnykh Soedinenii, No. 1, pp. 14–17, January–February, 2005. 相似文献
997.
Desmond A. Young Daneel Ferreira David G. Roux 《Journal of polymer science. Part A, Polymer chemistry》1986,24(5):835-849
The structure and stereochemistry of four synthetic “angular” tetraflavanoid-condensed tannin derivatives are examined by high-resolution variable temperature 1H NMR. spectroscopy, and hence correlated with their dynamic behavior. Three “angular” oligomers exist as stable rotational isomers at ambient temperatures, thus contrasting with the mobility about their interflavanoid bonds of most natural profisetinidin “trimeric” and “tetrameric” homologs. A “linear” tetraflavanoid analog results from one of these regioselectively controlled condensations. 相似文献
998.
Mariko Kusabe Hiromitsu Kozuka Satoru Abe Hiroshi Suzuki 《Journal of Sol-Gel Science and Technology》2007,44(2):111-118
Hydroxypropylcellulose (HPC)–titania hybrid thin films were prepared by sol–gel method where titanium tetraisopropoxide Ti(OC3H7
i
)4 was hydrolyzed under acidic conditions in the presence of HPC, followed by dip-coating and drying at 120 °C for 24 h. The
viscosity average molecular weight of HPC was 55,000–70,000 or 110,000–150,000, and the TiO2/(HPC + TiO2) mass ratio ranged from 0 to 1, which was calculated on the assumption that all Ti(OC3H7
i
)4 is converted into TiO2. The films were 0.35–1.0 μm thick, transparent in visible region and opaque in ultraviolet (UV) region, where the optical
absorption coefficient in UV region increased with increasing titania content. The refractive index increased with increasing
titania content, ranging from 1.6 to 1.8 for the hybrid thin films. The pencil hardness increased from 6B to 5H, the durability
in hot water significantly increased and the contact angle of water on films increased from 35° to 89° with increasing titania
content. Crack-free films could be deposited on organic polymer substrates irrespective of titania or HPC contents, where
cracking did not occur at higher HPC contents even when the substrate was bent. 相似文献
999.
用双氧水绿色氧化环己酮合成己二酸的研究 总被引:16,自引:0,他引:16
以30%的双氧水为氧化剂, 钨酸钠与含N或O的双齿有机配体(草酸)形成的络合物为催化剂, 在无有机溶剂、无相转移剂的条件下, 研究了环己酮氧化制己二酸的反应. 研究结果表明, 用廉价的草酸为配体, 最佳反应条件为钨酸钠∶草酸∶环己酮∶30%的双氧水的物质的量比为2.0∶3.3∶100∶350, 在92 ℃下反应12 h, 可制得80.6%的己二酸; 用GC-MS跟踪了氧化过程中三种主要物质环己酮、己内酯及己二酸含量随反应时间的变化关系, 提出了其主要氧化机理为环己酮首先经Beayer-Villiger氧化反应生成己内酯, 己内酯进一步氧化成己二酸. 相似文献
1000.
The stability of spontaneous thin layers and thin layers formed upon cathodical polarization of Ti in KOH solutions have been
studied by potentiostatic and ellipsometric methods. At open circuit potential (OCP) the strongly adherent films, whose thickness
depends on the concentration of the KOH solution, were formed. During the cathodic polarization the transformation of these
films to weakly adsorbed precipitated layers on the electrode surface was observed. Comparing the theoretically computed curves
with the experimental Ψ vs Δ loci measured ellipsometrically, the complex indices of refraction and the thickness of the generated films, from 3.6
to 60 nm in 1 M KOH and from 36 to 105 nm in 5 M KOH (adherent to the electrode surface), were determined. At OCP the rate
of film growth increases with increasing the concentration of KOH solution. Cathodic polarizations change the chemical composition
and retard the rate of film growth. Based on the ellipsometric and electrochemical data the chemical compositions of the formed
films consisted of TiO2, Ti2O3, TiO2·H2O, Ti(OH)3 and TiOOH·nH2O. 相似文献