162 resultados para 1995_01250722 TM-50 4302111


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Bond covalencies in R2BaCuO5 (R = Sm, Gd, Dy, Ho, Y, Er, Tm, Yb, Lu) were calculated by means of a semiempirical method. This method is the generalization of the dielectric description theory of Phillips-Van Vechten-Levine-Tanaka scheme. The present paper presents the formula concerning the decomposing of complex crystals which are usually anisotropic systems into the sum of binary crystals which are isotropic systems. It can be seen that although the bond covalency is related to many physical quantities, it is mainly influenced by bond valence or bond charge, and a higher bond valence will produce higher bond covalency.

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Extraction resins, of the type of;levextrel, (which is a collective term for styrene/divinylbenzene based copolymers of predominantly macroporous structure that contain a selective extractant) are important for the recovery and separation of metal ions, as they combine features of solvent extraction and ion exchange resins. This paper presents the results of the adsorption of heavy rare earth ions (Ho(III), Er(III), Tm(III), Yb(III), Lu(III) and Y(III)) from hydrochloric acid solutions at 0.2 mol/L ionic strength and 50 degrees C by the extraction resin containing di (2,4,4-trimethyl pentyl) phosphinic acid (Cyanex 272) and the chromatographic separation of (Er(III), Tm(III) and Yb(III)). Technological separation products, with purity and yield of Tm2O3 >99.97%, >80%, Er2O3 >99.9%, >94% and Yb2O3 >99.8%, >80% respectively, have been obtained from a feed having the composition Tm2O3 60%, Er2O3 10%, and Yb2O3 3%, the others 27%. The distribution coefficients, extraction equilibrium constants and separation factors have been determined as a function of acidity, loading of the resin and rare earths, flow rates and column ratios. The resolutions and efficiencies of separation of Er/Tm/Yb each other have been calculated. The stoichiometry of the extraction of rare earth ions has been suggested as well.

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RBa2Cu3O7 (R = Pr, Sm, Eu, Gd, Dy, Y, Ho, Er, Tm) has been studied using complex chemical bond theory. The results indicated that with the decreasing of R radius, the ionicities for all considered types of bond decrease. This is in good agreement with the experimental fact that T-c decreases with the decreasing of R radius. PrBa2Cu3O7 with no Ba-site Pr in this calculation is also predicted to be a superconductor. This supports the conclusion obtained by Blackstead et al. The ionicity for each bond obeys the following order: Ba-O > R-O > Cu(2)-O(1) > Cu(2)-O(2,3) > Cu(1)-O(4) similar to Cu(1)-O(1).

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研究了PA1010/66共聚物在液氮温度与Tm之间的松弛行为与组成的关系发现不同的松弛温度及损耗因子随共聚物组成的改变而变化的趋势不同随66含量增加,Tγ总趋势下降,Tβ总趋势增加,Tα先下降后增加;tanδ(γ)·tan-1δ(α)和tanδtan-1δ(α)先下降后增加,tanδ(α)先增大后减小。66占50%时,Tγ、Tβ极大,Tα最小;tanδ(γ)tanδ(β)、tanδ(β)·tan-1δ(α)最小,tanδ(α)最大.

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采用高温固相反应法,LiF/MgF2/AlF3=120/110/100,烧结温度为1008K,烧结时间为4h,在流动的高纯Ar中合成了LiMgAlF6:Tm3+。对其结构和发光特性进行了研究。

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The novel poly(aryl ether ketone)s containing chloro-side group were synthesized by nucleophilic substitution reactions of 4,4'-biphenol and chlorohydroquinone with either 4,4'-difluorobenzophenone(BP/CH/DF) or 1,4-bis(p-fluorobenzoyl)benzene (BP/CH/BF) and their thermotropic liquid crystalline properties were characterized by a variety of experimental techniques. The thermotropic liquid crystalline behavior was observed in the copolymers containing 50 and 70% biphenol. Melting transition (Tm) and isotropization transition (Ti) both appeared in the DSC thermograms. A banded texture was formed after shearing the sample in the liquid crystalline state. The novel poly(aryl ether ketone)s had relatively higher glass transition temperature (Tg) in the range of 168 similar to 200 degrees C and lower melting temperature (Tm) in the range of 290 similar to 340 degrees C. The thermal stability (Td) was in the range of 430 similar to 490 degrees C.

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本文利用顺磁稀土离子的诱导化学位移变化的性质,研究了多官能团配体谷胱甘肽(GSH)与稀土的配位作用.在水溶液中GSH通过分子两端的羧基负离子与稀土形成遥爪配位结构.谷氨酸端和甘氨酸端羧基与Eu~(3+)的配位稳定常数分别为12.5±0.1L/mol和100.0±0.5L/mol.从~(13)C化学位移的pH变化曲线求得谷氨酸端和甘氨酸端羧基解离的pK_a值分别为2.20±0.02和3.50±0.04.对Dy~(3+)、Ho~(3+)、Er~(3+)、Tm~(3+)和 Yb~(3+)作用下,GSH的~(13)C位移数据分析表明,配体与这些离子形成同构的配合物,分子两端羧基均可能以双齿形式与稀土配位.

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研究了水热法合成晶体,浓度配比、生长温度对晶体生长习性的影响.合成了一系列化学计量比的Y_(1-x-0.3)Er_(0.3)Tm_xP_5O_(14)(x=0.01~0.1)晶体,观察和分析了晶体的缺陷及成因,测定和讨论了晶体结构.

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Planktonic foraminiferal delta O-18 record for core DGKS9603 from the Okinawa Trough shows a series of climatic fluctuations and sudden cooling events in short time scale during 50 kaBP, which appear to correlate closely to the Younger Dryas and Heinrich events H1-5 recorded in Chinese loess, the South China Sea, the North Atlantic cores and the Greenland ice cores. Three polarity reversal events, correlating to Gothenburg, Mungo and Laschamp events, approximately correspond to Heinrich events H1, H3 and H5 respectively, which could be a cause of global climate changes. The delta O-18 curve of the Okinawa Trough is well associated with the grain size record of the Lijiayuan loess profile in northwestern China and is somewhat different from the climate fluctuations documented in the Greenland ice cores. These correlation results indicate that regional factors play an important role in controlling the climate changes in the East Asia, and the East Asian Monsoon could be the prominent regional controlling factor.

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以研究区2000 年TM影像、1:50 000 地形图和1:250 000DEM为基础数据源, 运用景观斑块分布与多样性特征指数, 测算了黔西南中低山丘原盆谷区不同岩性和地貌类型下景观格局特征。结果表明: ①灌木林地、疏林地、中覆盖度草地占据着景观中的优势地位, 是明显的景观基质, 控制着区域景观生态格局及其发展。景观斑块类型在不同岩石和地貌类型区存在较明显差异; ②在连续性灰岩区、灰岩与碎屑岩互层区和灰岩夹碎屑岩区形成的山间盆地和高原台面上以及北部水热丰富的河谷地带, 水田、旱地、疏林地、低覆盖度草地集中分布, 浅中切割低山类型中有林地和灌木林地集中分布; ③在连续性白云岩区形成的深切割( 低、中和高) 丘陵、浅切割( 低、中和高) 丘陵, 低覆盖度草地和灌木林地集中分布; ④从岩溶石漠化、土壤侵蚀、森林退化的空间格局及其组合来看, 在形成生态环境的区域差异过程中, 岩性和地貌的空间组合结构起着显著的控制作用。

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Urinary 8-hydroxydeoxyguanosine (80HdG) has been considered as an excellent marker of individuals at high risk of developing cancer. Until now, urinary 80HdG has largely been measured by high-performance liquid chromatography with electrochemical detection. A new method for the analysis of urinary 80HdG by high-performance capillary electrophoresis has been developed and optimized in our laboratory. A single step solid-phase extraction procedure was optimized and used for extracting 80HdG from human urine. Separations were performed in an uncoated silica capillary (50 cm x 50 tm i.d.) using a P/ACE MDQ system with UV detection. The separation of 80HdG from interfering urinary matrix components is optimized with regard to pH, applied voltage, pressure injection time and concentration of SDS in running buffer. The detection limit of this method is 0.4 mug/ml, the linear range is 0.8-500 mug/ml, the correlation coefficients levels is better than 0.999. The developed method is simple, fast and good reproducibility, furthermore, it requires a very small injection volumes and low costs of analysis, which makes it possible to provide a new noninvasive assay for an indirect measurement of oxidative DNA damage.