电感耦合等离子体原子发射光谱分析中不同电离电位元素基体效应的比较研究

选择不同电离电位的基体元素K、Na、La、Y和Mg,比较研究了它们对分析元素谱线强度的影响,其影响程度与谱线激发电位及基体元素电离电位有定量的相关关系。碱金属基体(K、Na)和非碱金属基体(La、Y和Mg)对分析元素检出限、背景强度及其相对标准偏差的影响显著不同,后者的记忆效应也大于前者。La的电离电位与Na相差不大。但其基体效应与Y相似,表明墓体效应与基体元素的化学性质有关。     

氢化物发生电感耦合等离子体原子发射光谱同时测定纯铜中氢化物和非氢化物形成元素

用新型氢化物发生喇叭口Ⅱ型同心雾化器替代Meinhard同心雾化器，溶液雾化为气溶胶和氢化物发生反应生成氢化物气体就可以在雾化系统中同时进行，选用L-巯基丙氨酸(L-cysteine)和硫脲(thiourea)作为基体铜的掩蔽剂，无需分离基体铜，实现了电感耦合等离子体原子发射光谱(ICP-AES)同时测定纯铜样品中氢化物和非氢化物形成元素的目的。研究了酸度、NaBH4的浓度、载气流速及清洗时间对氢化物形成元素的影响，考察了铜基体对氢化物形成元素的化学干扰情况。用本方法测定了纯铜标准样品(NIST SRM400)，结果令人满意。在1000mg/L纯铜样品溶液中，其氢化物形成元素As、Bi、Sb、Sn、Se和Te的检出限分别为0．08、0．15、0．10、0．17、0．21和0．23μg／L。     

8-羟基喹啉-5-磺酸纤维微柱分离富集电感耦合等离子体原子发射光谱法同时测定多种痕量元素

本文合成了8-羟基喹啉-5-磺酸纤维滤纸片,以此做为微柱填充物同时富集了10种痕量元素,并分离了样品中的高盐组分.本方法可使痕量组分的分离与富集同步进行,因而特别适用于原子光谱测定前样品的预处理.     

氨基羧酸纤维分离富集-电感耦合等离子体原子发射光谱法测定多种痕量稀土元素

本文制备了氨基羧酸纤维滤纸片作为柱填充物，成功地分离和富集了地化样品中的多种稀土元素。富集后的稀土元素采用电感耦合等离子体原子发射光谱法测定，回收率为90％～109％。本文还对基体干扰及其消除进行了研究。     

Thermal decomposition of struvite

Struvite (NH₄MgPO₄·6H₂O) is a mineral often found in urinary tracts and kidneys. Thermal decomposition using slow low heating shows that the 'kidney' stone can be decomposed at temperatures below 40°C. At this temperature both ammonia and water are evolved. If more rapid heating is employed the decomposition occurs at around 80°C. The implication of this work rests with the use of low slow heat for the decomposition of the kidney stones. This revised version was published online in July 2006 with corrections to the Cover Date.     

Comparison of the Dynamics of Water Molecules in Crystals of Proton-Ordered Ice IX and Its Proton-Disordered Analog III

A computer simulation of proton-ordered ice IX and its proton-disordered analog III (768 molecules, 90 K) was carried out by the molecular dynamics method using Poltev–Malenkov's potential. For ice IX, the differences in the dynamic characteristics of molecules with O(1) and O(2) are much wider than those in the case of ice III. The libration spectrum of ice IX has a number of distinct acute peaks, and the spectrum of ice III is strongly smoothed. These peculiarities are explained by the proton ordering of ice IX and disordering of ice III. The latter is responsible for the great differences in the short- and especially long-range environment of water molecules in ice crystals and hence for the presence of many molecules with different dynamic characteristics. Thus averaging over a large number of different vibrational spectra of molecules leads to a smoothed total spectrum in the case of the proton-disordered crystal modification of ice.     

Metrological role of neutron activation analysis. IB. Inherent characteristics of relative INAA as a primary ratio method of measurement

This is the second part of a paper which deals with the advantages and disadvantages of relative instrumental neutron activation analysis concerning traceability and uncertainty, and the current scope and possible future extensions of neutron activation analysis as a primary ratio method. The first part of this paper has been published in this Journal [1]. Received: 19 March 2001 Accepted: 2 October 2001     

Strained Structure in Ho0.5Sr0.5MnO3

The Ho_0.5Sr_0.5MnO₃ perovskite, synthesized in air, has been studied by combining neutron powder and electron diffraction techniques. The Pnma-type structure exhibits a strong tilting of the MnO₆ octahedra. This octahedra tilting and microtwinning involve a complex strained structure. No structural transition is observed down to 1.4 K, but short-range A-type antiferromagnetism running over only a few perovskite subcells is evidenced below ≈90 K. The different behavior of this perovskite compared to other Ln_0.5Sr_0.5MnO₃ perovskites is discussed in terms of A-site cationic mismatch.