Column solid phase extraction using solid sorbent [Foam-Pap -hexamethyleneammonium hexamethylenedithiocarbamate (HMDC) immobilized on polyurethane (PU) foam mixed with methyltrioctylammonium chloride (MTOAC) immobilized on filter paper as well as the solid sorbent PU-HMDC-MTOAC mixture of the above
Determination of trace zirconium and hafnium in high-purity scandium oxide by inductively coupled plasma atomic emission spectrometry and extraction chromatography
โ Scribed by Xiao-Jin Yang; Jing-Su Guan; Tai-Jun Shen
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 507 KB
- Volume
- 277
- Category
- Article
- ISSN
- 0003-2670
No coin nor oath required. For personal study only.
โฆ Synopsis
Inductively coupled plasma atomic emission spectrometry in combination with extraction chromatography was applied to the determination of trace amounts of zirconium and hafnium in high-purity scandium ozide. The chromatographic column separation procedure was carried out with 1-phenyl-3-methyl-4-benzoylpyrazol-5-one as the stationary phase and hydrochloride acid as the mobile phase. Optimum cobunn operating conditions were established. The enrichment factor based on 0.1 g of scandium oxide was over 2000. The results obtained agreed well with those obtained by spark-source mass spectrometry without the separation of scandium. For a sample mass of 0.3 g, the detection limits for zirconium and hafnium were 0.14 and 0.17 kg g-l, respectively. The proposed method could be applied to the analysis of scandium ozide of laser grade and 99.9995% purity.
๐ SIMILAR VOLUMES
A study was made to investigate the feasibility of using an anion-exchange resin for on-line separation of trace amounts of niobium, tantalum, tungsten, zirconium and hafnium from iron matrix samples. The incorporation of a micro-column packed with Dowex 1X8-100 ion-exchange resin into a flow inject
A desolvation device was connected to a microcolumn (40 mm X 3.0 mm i.d.) in which 8-hydroxyquinoline-5sulphonic acid was immobilized on the substrate of active carbon-silica gel. The analyte and 1.0 M sodium acetate-acetic acid buffer solution (pH 5.6) were mined and pumped through the microcolumn.
A simple and rapid method has been developed for the determination of molybdenum and vanadium in seawater using ion-exchange preconcentration and inductively coupled plasma atomic emission spectrometry (ICP-AES). One hundred milliliters of seawater prepared as \(0.05 M\) hydrochloric acid solution i
An mductlvely coupled plasma atomic emlsslon spectrometrlc WP-AES) method for the determmatlon of lanthamdes and yttrmm m rare earth ores and concentrates 1s described After a smtable separation of these elements from the other matru( constituents, a mtnc solution of rare earth elements was obtained