Ni（Ⅱ）—MOBTAMB—TritonX—100体系析相光度法测定痕量镍

研究了Triton X-100在浊点条件下,对Ni(Ⅱ)-2-[2′-(6′-甲氧基-苯并噻唑)偶氮]-5-二甲氨基苯甲酸(MOBTAMB)配合物的析相条件。在pH 8.6～9.5的氨-氧化铵缓冲体系中,90℃水浴加热1.5h,析相完全。配合物最大吸收峰位于658nm处,表观摩尔吸光系数为5.5×10~5。镍含量在0～3μg/30ml范围内符合比耳定律。所拟方法用于天然水中的痕量镍测定,结果满意。     

IPv4/IPv6翻译网关的研究

In this paper, a model of translation gateway is proposed. The communications between IPv4 network and IPv6 network are realized by using the Microsoft intermediate driver technology in environment of Windows 2000.     

ZK—4、NaANaHS3种沸石的铝化

用高温气－固相置换法对ZK－4、NaANaHS3种沸石进行铝化。组成分析、尾气分析、X射线衍射、晶体形貌分析、红外光谱和^29Si高分辨魔角固体核磁结果表明，3种低硅铝比沸石铝化后骨架可能存在Al-O-Al键。     

高温超导体磁通动力学和混合态相图(Ⅱ)

（上接2006年第1期第16页） 5涡旋态相图的发展 随着理论和实验工作的不断进展，高温超导体混合态相图变得丰富多彩．首先在涡旋玻璃态理论出现后，相图就较常规超导体有了很大的变化．在常规超导体中，相图上就只有两根标志相边界的线。     

F－L模型的状态方程与退禁闭相变图象

用温度场论方法计算了Ｆ－Ｌ模型在有限温度和密度下的状态方程，分析了压强对净重子数密度的等温线．结果表明，在平均场近似下，Ｆ－Ｌ模型所给出的退禁闭相变为一级相变．     

动力学自发破缺的模型在有限温度和密度下的状态方程和相结构

本文在Lurie模型的基础上,建立了一种近似计算状态方程的方法.得到了Lurie模型的状态方程所满足的参数方程.该模型的手征相变的相图表明:存在一个临界点c将一级相变和二级相变分开.仔细分析压强对净重子数密度的等温线,其结果表明:发生一级相变时,有过冷和过热的亚稳态,存在有自发破缺的破缺相和无自发破缺的正常相的两相共存.     

相函数具退化临界点的振荡积分

考虑相函数具退化临界点的振荡积分. 在相函数的有限型条件下, 得到第1型振荡积分的估计. 该振荡积分的衰减依赖于有限型、空间维数及象征的指标.     

Magnetic Properties of Hf0.8Ta0.2（Fe0.97A0.03）2 （A=Al, Co, Mn） Systems

Moessbauer studies on the effect of substitution with 3% Al, Co, Mn atoms in the intermetallic compound of Hf0.8Ta0.2Fe2 are reported. The Al substitution leads to increase of the FM-AFM transition temperature and to decrease of the AFM-PM transition temperature. The Co substitution leads to disappearance of the FM state, only showing some FM impurity component, while Mn substituted compound indicates coexistence of FM and AFM states at low temperature. The phenomena imply complex itinerant electron properties in these magnetic systems.     

SYNTHESIS OF POLYMER—SUPPORTED PALLADIUM CATALYSTS AND THEIR CATALYTIC BEHAVIOR FOR THE SELECTIVE HYDROGENATION OF MESITYL OXIDE

Copolymer of styrene-divinylbenzene in bead from was made by suspension polymerization.After chloromethylation and amination,five kinds of polymeric amines were thus obtained.These polymers were reacted with palladium chloride,and were then reduced.The polymer-supported catalysts synthesized above were used to catalyze the selective hydrogenation of mesityl oxide under reaction conditions of 80℃ and 10kg/cm^2,using methanol as a solvent.The catalytic activity and MIBK(methyl isobutyl ketone) formation selectivity of the catalysts were examined.     

TrpH—TryOH肽链中电子的逆向转移

本文较详细的研究了色氨酰酪氨酸二肽（ＴｒｐＨ－ＴｙｒＯＨ）中的电子转移，电子该电子转移的速率，甚至电子转移的方向都强烈的依赖于溶液的ｐＨ。而且，该肽中的酪氨酸残基瞬态粒子浓度与色氨酸残基瞬态粒子浓度之比也强烈的依赖于ｐＨ。根据这种依赖性，求得了二肽中的ｐＫａ（ＴｒｐＨ＾＋）和ｐＫａ（ＴｙｒＯＨ），其值分别为６．２和１１．３。