LaPO4纳米微粒的制备及表征

Surface-modified LaPO4 nanoparticales were synthesized in the mixture solvent of water-ethanol with the surface modification age of dialkylphosphate. The conditions of synthesis and characterization were discussed. The results indicated that nanoparticle core of LaPO4 and surface-modified layer were formed. The surface-modified nanoparticles of LaPO4 can be dispersed in organic solvent and has better lubricating properties.     

稀土丙烯酸盐与8－羟基喹啉三元固态配合物的合成与表征

稀土丙烯酸盐与８－羟基喹啉三元固态配合物的合成与表征李长正，王学智，唐宁，谭民裕（兰州大学化学系兰州７３００００）关键词：稀土，丙烯酸，８－羟基喹琳，三元配合物８－羟基喹琳因其具有优良的配位性能而被广泛应用于金属离子的分离和分析中［１］。文献中有关它...     

一类新的4-取代胂酸型变色酸偶氮多卤显色剂的合成及其与稀土元素显色反应的研究

本文研究了五个结构新颖的显色剂与稀土元素的显色反应。其中的二溴羧基偶氮氯肿(CAsA-DBK)与稀土元素反应具有对比度大、灵敏度高、选择性好等优点。在0.6mol/LHClO_4介质中,不加任何掩蔽剂条件下,只与铈组稀土显色,与钇组稀土几乎不显色,是一个较有特色的铈组稀土试剂。     

New Rare Earth（Ⅲ） Complexes with H2tmtaa

A series of Ln(tmtaa)(Htmtaa)·CH_2Cl_2(Ln=Sm,Tb,Er and Yb)complexes were prepared and characterized byinfrared spectra,mass spectra and molecular electronic spectroscopy as well as DSC measurement.A sandwichstructure containing all the eight nitrogen atoms of tmtaa and Htmtaa was proposed for these complexes.X-rayphotoelectron spectra(XPS)of these complexes revealed that four nitrogen atoms of both tmtaa and Htmtaa werechemically equivalent to each other,respectively.The acidic hydrogen of Htmtaa did not bind specifically to any ni-trogen atom of Htmtaa,but was shared by all the four nitrogen atoms.The magnetic properties of these complexeswere found to be in good agreement with their theoretical values.     

Quantitative surface analysis by Auger and x-ray photoelectron spectroscopy

Recent developments in quantitative surface analysis by Auger (AES) and x-ray photoelectron (XPS) spectroscopies are reviewed and problems relating to a more accurate quantitative interpretation of AES/XPS experimental data are discussed. Special attention is paid to consideration of elementary physical processes involved and influence of multiple scattering effects on signal line intensities. In particular, the major features of core-shell ionization by electron impact, Auger transitions and photoionization are considered qualitatively and rigorous approaches used to calculate the respective transition probabilities are analysed. It is shown that, in amorphous and polycrystalline targets, incoherent scattering of primary and signal Auger and photoelectrons can be described by solving analytically a kinetic equation with appropriate boundary conditions. The analytical results for the angular and energy distribution, the mean escape depth, and the escape probability as a function of depth of origin of signal electrons as well as that for the backscattering factor in AES are in good agreement with the corresponding Mote Carlo simulation data. Methods for inelastic background subtraction, surface composition determination and depth-profile reconstructions by angle-resolved AES/XPS are discussed. Examples of novel techniques based on x-ray induced photoemission are considered.     

Characterization of high-temperature superconductors by electron microprobe analysis

In order to optimize the physical properties of HTSC small single crystals grown from a melt for basic studies of their physical properties the influence of the environment on their impurity content was investigated by EPMA. This requires quantitative analysis of all elements being present in the crystals. The accuracy of results was affected by problems with the choice and quality of standards, by contamination but also by malfunction of microprobe electronics. The HTSC materials were found to react with mills, milling balls, crucibles and the atmosphere. These problems are being discussed and some reactions being studied for Y₁Ba₂Cu₃O_6+x (0 < x < 1) HTSC in A1₂O₃ and ZrO₂ crucibles. The crystals grown contain reproducible amounts of impurities depending on boundary conditions and exhibit a zone structure in composition particularly for Y and Ba within their range of homogeneity.     

Addition of nitriles to alkaline earth metal complexes of 1,2-bis[(phenyl)imino]acenaphthenes

Compounds [Sr(dpp-bian)(thf)4] (2), [Ba(dpp-bian)(dme)2.5] (3) and [Mg(dtb-bian)(thf)2] (4) (dpp-bian = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene; dtb-bian = 1,2-bis[(2,5-di-tert-butylphenyl)imino]acenaphthene) were prepared by reduction of dpp-bian and dtb-bian with an excess of metallic Mg, Sr, or Ba in THF or DME. Reactions of [Mg(dpp-bian)(thf)3], 3, and 4 with diphenylacetonitrile gave keteniminates [Mg(dpp-bianH)(NCCPh2)(thf)2] (5), [Mg(dtb-bianH)(NCCPh2)(thf)2] (6), and [Ba(dpp-bianH)(NCCPh2)(dme)2] (7), respectively. The reaction of 2 with CH3C[triple chemical bond]N in THF gave [{Sr(dpp-bianH)[N(H)C(CH3)C(H)CN](thf)}2] (8). The compounds 2, 3, 5-8 were characterized by elemental analysis, and IR and NMR spectroscopy. Molecular structures of 2, 3, 7, and 8 were determined by single-crystal X-ray diffraction. In contrast to reactions of alkali-metal reagents, magnesium amides, or yttriumalkyls with alpha-H acidic nitriles, which are accompanied by an amine or an alkane elimination, the reactions of [Mg(dpp-bian)(thf)3] (1), 2, 3, and 4 with such nitriles proceeded with formation of Mg, Sr, and Ba keteniminates and simultaneous protonation of one nitrogen atom of the bian ligand. The NMR spectroscopic data obtained for complex 5 indicated that in solution the amino hydrogen atom underwent the fast (on the NMR timescale) shuttle transfer between both nitrogen atoms of the dpp-bianH ligand.     

Influence of the texture of chromia catalysts on their activity in synthesis of 2-methylthiophene

The texture of Cr₂O₃-K₂O/Al₂O₃catalysts containing oxides of rare earth elements (REE) was studied. The catalysts are used for the synthesis of 2-methylthiophene by the reaction of H₂S with n-pentane or piperilene. The heterocyclization of n-pentane is a consecutive reaction involving a step of dehydrogenation of initial hydrocarbon. At this step the texture of the catalyst affects the yield of 2-methylthiophene. The yield of 2-methylthiophene obtained from piperilene and I₂S is independent of the catalyst texture.