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排序方式: 共有1002条查询结果,搜索用时 15 毫秒
1.
Takayuki Nakai Yoshiko Murakami Yoshiaki Sasaki Isamu Fujiwara Shoji Tagashira 《Analytical sciences》2004,20(1):235-237
The extraction and separation of copper(II), zinc(II), cobalt(II), and cadmium(II) were investigated. Both copper(II) and zinc(II) formed ammine-complexes, while cadmium(II) and cobalt(II) formed hydroxide precipitates in an ammonia medium. By the addition of sodium dodecylsulfate (SDS), a copper(II) complex formed an ion-pair (copper-ammine-DS), which was extracted into the SDS phase. However, a zinc(II) complex did not form an ion-pair, and was soluble in water. Copper(II) ion was recovered by stripping (back-extraction) after the addition of hydrochloric acid. This method was applied to the separation of copper(II) in a brass alloy. 相似文献
2.
A large-volume (100 microl) injection-ETAAS with W-treated PG furnace combined with a phosphate modifier was applied to the determination of unpolluted levels of Cd in tap, snow and river-water samples. The limit of detection of 1.1 ng l(-1) was observed for a 4 w/v% NH4H2PO4 modifer. Matrix interference studies were tested for major ion species well found in fresh water. The direct determination of Cd in certified river water (12 +/- 2 ng l(-1)) was carried out and the observed value was in agreement with the certified one. The good recoveries of Cd added to real environmental water samples were also observed. This method was applied to the determination of Cd in unpolluted environmental water samples. 相似文献
3.
An automated on-line sample-preparation method using a computer-controlled pretreatment system (Auto-Pret AES system) coupled with ICP-AES was developed. In this work, an iminodiacetate chelating resin, packed in a mini-column and installed in the system was employed for the collection/concentration of 13 trace metals, including such toxic metals as Be, Cd, Cr, Cu and Pb. The limits of detection of the proposed method for trace metals were in the range of 0.001 (Be) -0.18 (Pb) ng mL-1. The enrichment factors for metal ions were about 19 times, when 5 mL of samples were used. The sample throughput was 11 h-1. The accuracy and the precision of the method were evaluated using river-water reference materials, SLRS-4 from NRCC, JSAC 0301-1 and JSAC 0302 from the Japan Society for Analytical Chemistry. The proposed method can be favorably applied to the collection/concentration of trace metals in natural water samples. 相似文献
4.
The removal of excess reagent extracted into an organic phase in the solvent extraction of a metal complex anion with a quaternary ammonium ion is discussed. With a given chelating ligand (HO—R—SO3H), the order of extractability is HO—R—SO3- > M(OR—SO3)n- > X- > -O—R—SO3- when an anion such as nitrate or halide is added. If suitable amounts of the anion are added, only the excess of reagent can be removed. The principle is applied to the extraction with zephiramine of the cobalt complex anion formed with 2-nitroso-1-naphthol-4-sulfonic acid. Micro amounts of cobalt in pure nickel salts were determined spectrophotometrically. 相似文献
5.
The simple removal of excess of co-extracted reagent in the solvent extraction of metal complex anions with a quaternary ammonium salt greatly improves the determination of iron(II) with pyrogallol red and zephiramine. The method with pyrogallol red is suitable for the determination of trace amounts of iron in natural waters. The apparent molar absorptivities of the iron(II) complex in chloroform are 7.5×104 and 10.3×104 1 mol-1 cm-1 at 560 and 298 nm, respectively. A large excess of reagent can be added, and the ternary complex can be completely extracted over the pH range 8.5–10. Masking agents allow most interferences to be suppressed. The method is suitable for the analysis of potable, river and sea waters. 相似文献
6.
7.
Ken-ichi Sato Shoji AkaiToshiyuki Hiroshima Hidenori AokiMayumi Sakuma Ken-ju Suzuki 《Tetrahedron letters》2003,44(17):3513-3516
The chemoenzymatic synthesis of 13C-labeled sialic acid (NeuAc) and 3-deoxy-d-glycero-d-galacto-2-nonulosonic acid (KDN) as useful molecular probes for studying the conformation of sialyl or KDN oligosaccharides attached to proteins was performed by using [6-13C]-ManNAc, [6-13C]-Man and [3-13C]-pyruvic acid sodium salt. In the synthesis of the compounds, 5,6-anhydro intermediates were found to easily provide not only 6-13C-labeled but also 5-, and 6-modified NeuAc and KDN analogs. Furthermore, it was demonstrated that identical results are obtained by NMR for both [3,9-13C]-NeuAc and 1:1 mixtures of [3-13C]- and [9-13C]-NeuAc. 相似文献
8.
Energy distributions of He+ ions scattered by Au and Ag surfaces are measured by an ISS system with high energy resolution, at a scattering angle of 90° and at incident ion energies ranging from 277 to 977 eV. It is found that the observed peak energies deviate toward the low energy side by several electron-volts with respect to the calculated elastic single collision energies. Both the deviation Q' and the inelastic loss energy Q are plotted as a function of incident ion energy for the Au surface. 相似文献
9.
10.
The growth process of silver on a Si(111) substrate has been studied in detail by low-energy ion-scattering spectroscopy (ISS) combined with LEED-AES. Neon ions of 500 eV were used as probe ions of ISS. The ISS experiments have revealed that the growth at room temperature and at high temperature are quite different from each other even in the submonolayer coverage range. The following growth models have been proposed for the respective temperatures. At room temperature, the deposited Ag forms a two-dimensional (2D) island at around 2/3 monolayer (ML) coverage, where the Ag atoms are packed commensurately with the Si(111)1 substrate. One third of the substrate Si surface remains uncovered there. Then it starts to develop into Ag crystal, and at a few ML coverage a 3D island of bulk Ag crystal grows directly on the substrate. An intermediate layer, which covers uniformly the whole surface before the growth of Ag crystal, does not exist. At high temperatures (>~200°C), the well-known Si(111)√3-Ag layer is formed as an intermediate layer, which consists of 2/3 ML of Ag atoms and covers the whole surface uniformly. These Ag atoms are embedded in the first double layer of the Si substrate. It is concluded that the formation of the √3 structure needs relatively high activation energy which may originate from the large displacement of Si atoms owing to the embedment of the Ag atoms, and does not proceed below about 200°C. The most stable state of the Ag atoms on the outermost Si layer is in the shape of an island, both for the Si(111) surface and for the Si(111)√3-Ag surface. 相似文献