Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/11866
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dc.contributor.authorRatanawimarnwong N.
dc.contributor.authorRuckchang P.
dc.contributor.authorYooram S.
dc.contributor.authorSongsrirote K.
dc.contributor.authorUraisin K.
dc.contributor.authorCerdà V.
dc.date.accessioned2021-04-05T03:01:19Z-
dc.date.available2021-04-05T03:01:19Z-
dc.date.issued2021
dc.identifier.issn17599660
dc.identifier.other2-s2.0-85099781035
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/11866-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85099781035&doi=10.1039%2fd0ay01970d&partnerID=40&md5=9f817ad1a0c2a794e1282b56c99f6dc9
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 is © The Royal Society of Chemistry.
dc.rightsSrinakharinwirot University
dc.subjectAzo dyes
dc.subjectChemical reactions
dc.subjectChlorine compounds
dc.subjectMercury compounds
dc.subjectSodium Borohydride
dc.subjectTrace analysis
dc.subjectVaporization
dc.subjectAbsorbance change
dc.subjectAcidic conditions
dc.subjectDetection limits
dc.subjectHydride generations
dc.subjectHydronium ions
dc.subjectMercuric chloride
dc.subjectMethyl Orange
dc.subjectTotal arsenics
dc.subjectSurface waters
dc.titleDevelopment of a microfluidic membraneless vaporization flow system for trace analysis of arsenic
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationAnalytical Methods. Vol 13, No.2 (2021), p.202-211
dc.identifier.doi10.1039/d0ay01970d
Appears in Collections:Scopus 1983-2021

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