Bioparticles coated with an ionic liquid for the pre-concentration of rare earth elements from microwave-digested tea samples and the subsequent quantification by ETV-ICP-OES† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6ay02189a Click here for additional data file.
نویسندگان
چکیده
An analytical procedure for straight-forward quantification of rare earth elements (REEs) in tea was developed. The method consists of three steps: first, dry tea powder is converted into an aqueous sample solution using a microwave-assisted digestion procedure. Then, the REEs are retained on newly designed sorbent particles and are thus effectively extracted from the sample digest. Then, the REEloaded sorbent material is introduced into the furnace of an electro-thermal vaporization (ETV) unit. There, the core of the particles is pyrolyzed and removed in a first temperature step. Then, the REE analytes are swiftly evaporated at high temperatures, and subsequently analyzed by ICP-OES. The advantages of the method proposed here are as follows: extraction of REEs is accomplished via “dispersed particle extraction”; this avoids typical shortcomings of conventional solid-phase extraction. The analysis via ETV allows separation of the sorbent particles from the analytes in time. Thus, detrimental effects of plasma-loading are circumvented. The method was shown to provide satisfactory detection limits of typically 50 ng g 1 in the dry tea samples (3 s criterion). The method was validated by means of spike recovery experiments, and applied to the analysis of ten different tea samples from China, Japan and India, as sold in European markets.
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State Key Laboratory of Rare Earth Reso Applied Chemistry, Chinese Academy of Sc E-mail: [email protected]; [email protected] State Key Laboratory of Inorganic Synthes Chemistry, Jilin University, Changchun 1300 Department of Radiology, The Second H 130022, P. R. China † Electronic supplementary information (E supplementary gures and table of relax Mn-based nanoparticles. See DOI: 10.1039 Cite th...
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