一种符合ISO 14651语义的藏文排序实现方法

本文介绍了一种实现藏文字典序排序的方法,它针对藏文"大字丁字符集"编码方案.通过引入有(无)前加基字符的概念,它把待排序的藏字预处理为有(无)前加基字符、前加字符、基字(基字符或者字丁)、后加字符、再后加字符串后,再行比较,从而避免拆分字丁.本实现方法符合ISO/IEC14651标准语义.

ISO 2022的有限状态机描述

ISO 2022编码体系对字符集国家标准的制订有很大影响,然而标准条款存在不确定性,有时难于理解。本文引入有限状态机(FSM)模型来形式化地刻画ISO 2022的特征。针对FSM五元组,详细说明了其状态空间的构成,提出了输入字母表的等效分类方法,给出了初始状态以及终结状态集合,分析了状态转移函数的规模,并采用FSM描述方法分析了ISO-2022-CN、EUC-CN、复合文本等标准,揭示了这些标准与ISO 2022的内在联系。这些工作有助于ISO 2022标准符合性检测、扩展标准的制订与系统实现复杂度评估。鉴于形式化描述方法在编码字符集标准领域未得到广泛应用,本文工作为该类研究引入了新的思路和方法。

基于ISO/IEC10646标准的藏文操作系统若干问题研究

长期以来尚未有完整的藏文操作系统,原因是藏文文字的特性要求特定的文字处理。本文基于ISO/IEC10646的藏文字符集标准,结合藏文正字法要求,详细分析了藏文操作系统实现中的关键问题:(1)藏文字符集方案比较与藏文存储;(2)藏文输入;(3)藏文显现。藏文显现是公认的“瓶颈”问题。对此,本文提出基于音节划分、使用OpenType字体及相应的文本引擎来解决藏文“叠加”字符的显现。此方案应用于Qt库的实验及相关测试证明基于ISO/IEC10646标准的藏文操作系统实现是较合理的方案。

Solvent extraction study of protactinium(V) with methyl-iso-butyl carbinol and methyl-iso-butyl ketone

In order to study the extraction pattern of protactinium in different types of extracting agents and compare the similarity of patterns of extraction with dubnium and thereby unraveling its chemistry, solvent extraction of protactinium(V) with methyl-iso-butyl carbinol (MIBC) and methyl-iso-butyl ketone (MIBK) was studied using Pa-233 as a radiotracer. The extraction efficiencies of Pa were determined as a function of shaking time, concentrations of mineral acids, and extractant concentrations using the two extractants. The results show that MIBK is more suitable for the extraction of protactinium than MIBC in benzene. Furthermore, the effect of the F anion is also discussed.

Liquid-liquid extraction of protactinium(V) using tri-iso-octylamine

Solvent extraction of protactinium with tri-iso-octyl-amine (TIOA) in xylene, benzene, carbon tetrachloride and chloroform from HCl, HF, HNO3, HClO4 and H2SO4 media was studied using Pa-233 as a radiotracer. The extraction efficiencies of protactinium were determined as a function of shaking time, concentrations of mineral acids in aqueous phase, extractant concentrations and diluents in organic phase. The extraction mechanism was discussed. The results show that the extracted species in the organic phase is [(R3N-H)(n)Pa(OH)(x)Cl-y(5-x-y)].

Theoretical study on the formation mechanism of Iso-CH2I-Cl

The dissociation and isomerization reaction mechanism on the ground-state potential energy surface for CH2ClI are investigated by ab initio calculations. It is found that the isomer iso-CH2I-Cl can be produced from either the recombination of the photodissociation. fragments or the isomerization reaction of CH2ClI, rather than from isomerization reaction of iso-CH2Cl-I. Further explanations of experimental results are also presented. (C) 2003 Wiley Periodicals, Inc.

Surface-enhanced resonance Raman spectroscopic study of yeast iso-1-cytochrome c and its mutant

The structural stability and redox properties of yeast iso-1-cytochrome c and its mutant, F82H, were studied by surface-enhanced resonance Raman scattering (SERRS) spectroscopy. Phenylalanine, which exists at the position-82 in yeast iso-1-cytochrome c, is replaced by histidine in the mutant. The SERRS spectra of the proteins on the bare silver electrodes indicate that the mutant possesses a more stable global structure with regard to the adsorption-induced conformational alteration. The redox potential of the mutant negatively shifts by about 400 mV, relative to that of yeast iso-1-cytochrome c. This is ascribed to axial ligand switching and higher solvent accessibility of the heme iron in the mutant during the redox reactions.

X-ray crystal structure and molecular mechanics calculations of (2,6-iso-dipropyl-phenylamide) dimethyl (tetra-methylcyclopenta-dienyl) silane titanium dichloride

Crystal and molecular structure of (2.6-dipropylphenylamide) dimethyl (tetra-methyl cyclopentadienyl) silane titanium dichloride (I) was fully characterized by X-ray diffraction. The crystal is obtained from a mixture of ether/hexane as orthorhombic. with a = 12.658 (3) Angstrom. b = 16.62 (3) Angstrom. c = 11.760 (2) Angstrom. V = 2474.2 (9) Angstrom(3). Z = 4, space group Pnma. R = 0.0399; Componud I compose of the pi-bounded ring with its dimethylsilyl-dipropyl phenyl amido group and the two terminal chloride atoms coordinated to central metal to form a so-called constrained geometry catalyst (CGC) structure. The result of molecular mechanics (MM) calculations on compound I shows that bond lengths and bond angles from the MM calculation are comparable to the data obtained from the X-ray diffraction study. The relation of the structure of CGCs and their catalytic activity by MM calculations is also discussed.

THE EFFECT OF MOBILITY OF MOLECULES ON RADIATION-INDUCED CHAIN SCISSION AND RACEMIZATION OF ISO-POLY(METHYL METHACRYLATE)

The radiation-induced chain-scission and racemization of isotactic poly(methylmethacrylate)(iso-PMMA) in amorphous and semi-crystalline state as well as in solution have been studied with nuclear magnetic resonance and molar mass deter-mination. It is shown that the chain-scission is dominant for iso-PMMA in dilute solution while the racemization reaction is not favorable in this case. On the contrary, the racemization is favorable when iso-PMMA was irradiated in its crystalline state while chain-scission is not. Such experimental results could be well explained by the mobility of molecules and "cage effect". The hypothesis, we proposed previously that the chain-scission, racemization and recombination are in competition and the final result depends on the state of molecular motion at which iso-PMMA was irradiated, has been verified verified once again.

分子活动性对iso-PMMA辐射裂解和消旋的影响

以全同立构聚甲基丙烯酸甲酯(iso-PMMA)为对象,用核磁共振谱和分子量测定等手段,研究了不同物理状态,即无定型固态,结晶态和稀溶液状态下的辐射裂解和辐射消旋反应.结果表明,在稀溶液状态下辐照,其裂解反应最强,而消旋反应最弱;结晶状态下辐照,则裂解反应最弱而消旋反应最强.这充分说明了分子的活动性对反应的影响,进一步验证了前已提出的高分子链断裂-重合-消旋的平衡反应机理.