Publication:
Development of a microfluidic membraneless vaporization flow system for trace analysis of arsenic

dc.contributor.authorNuanlaor Ratanawimarnwongen_US
dc.contributor.authorPatcharat Ruckchangen_US
dc.contributor.authorSupattra Yooramen_US
dc.contributor.authorKriangsak Songsriroteen_US
dc.contributor.authorKanchana Uraisinen_US
dc.contributor.authorVictor Cerdàen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversitat de les Illes Balearsen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.contributor.otherFlow Innovation-Research for Science and Technology Laboratories (FIRST Labs)en_US
dc.date.accessioned2022-08-04T08:19:45Z
dc.date.available2022-08-04T08:19:45Z
dc.date.issued2021-01-14en_US
dc.description.abstractA 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. This journal isen_US
dc.identifier.citationAnalytical Methods. Vol.13, No.2 (2021), 202-211en_US
dc.identifier.doi10.1039/d0ay01970den_US
dc.identifier.issn17599679en_US
dc.identifier.issn17599660en_US
dc.identifier.other2-s2.0-85099781035en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/76549
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099781035&origin=inwarden_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.subjectEngineeringen_US
dc.titleDevelopment of a microfluidic membraneless vaporization flow system for trace analysis of arsenicen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099781035&origin=inwarden_US

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