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Development of a microfluidic membraneless vaporization flow system for trace analysis of arsenic.
Ratanawimarnwong, Nuanlaor; Ruckchang, Patcharat; Yooram, Supattra; Songsrirote, Kriangsak; Uraisin, Kanchana; Cerdà, Victor.
Afiliação
  • Ratanawimarnwong N; Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Bangkok 10110, Thailand. nuanlaorr@g.swu.ac.th and Flow Innovation-Research for Science and Technology Laboratories (Firstlabs), Thailand.
  • Ruckchang P; Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Bangkok 10110, Thailand. nuanlaorr@g.swu.ac.th.
  • Yooram S; Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Bangkok 10110, Thailand. nuanlaorr@g.swu.ac.th.
  • Songsrirote K; Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Bangkok 10110, Thailand. nuanlaorr@g.swu.ac.th.
  • Uraisin K; Flow Innovation-Research for Science and Technology Laboratories (Firstlabs), Thailand and Department of Chemistry, Center of the Excellence for Innovation in Chemistry, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
  • Cerdà V; Department of Chemistry, University of the Balearic Islands, 07122 Palma de Mallorca, Spain.
Anal Methods ; 13(2): 202-211, 2021 01 21.
Article em En | MEDLINE | ID: mdl-33331839
A new design of a membraneless vaporization (MBL-VP) unit coupled with a specific flow system is presented for the determination of arsenic at trace levels using a hydride generation process. The MBL-VP unit contains two concentric conical reservoirs, with the outer cone selected as the donor reservoir. The volume of the outer donor reservoir is thereby greater than the acceptor volume, necessary for holding sufficient sample and reagents for the generation of arsine gas by reaction between As(iii) and sodium borohydride under acidic conditions. The arsine gas diffuses into the narrow headspace and is absorbed by an aliquot of 150 µL of mercuric chloride acceptor solution. The resulting reaction produces hydronium ions which is monitored by the absorbance change at 530 nm of the methyl orange indicator added in the acceptor solution. To decrease the detection limit, the aspiration and removal of the donor plug, comprising the sample, borohydride and acid, into and out of the donor cone are repeated several times, while the acceptor solution is kept unchanged. As a result, analysis of arsenic was achieved in the range of 10 to 100 µg L-1 with a detection limit of 8 µg L-1. Application to surface water was investigated. Percent recoveries of spiked surface water samples were in the range of 94-110%. For comparison of total arsenic (As(iii) and As(v)), the results obtained from the developed method are not statistically different from the ICP-OES method.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Anal Methods Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Tailândia País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Anal Methods Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Tailândia País de publicação: Reino Unido