Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/58467
Full metadata record
DC FieldValueLanguage
dc.contributor.authorWanpen Khongpeten_US
dc.contributor.authorSomkid Penchareeen_US
dc.contributor.authorChanida Puangpilaen_US
dc.contributor.authorSupaporn Kradtap Hartwellen_US
dc.contributor.authorSomchai Lapanantnoppakhunen_US
dc.contributor.authorJaroon Jakmuneeen_US
dc.date.accessioned2018-09-05T04:24:53Z-
dc.date.available2018-09-05T04:24:53Z-
dc.date.issued2018-01-15en_US
dc.identifier.issn00399140en_US
dc.identifier.other2-s2.0-85029746236en_US
dc.identifier.other10.1016/j.talanta.2017.09.018en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85029746236&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58467-
dc.description.abstract© 2017 Elsevier B.V. A microfluidic hydrodynamic sequential injection (μHSI) spectrophotometric system was designed and fabricated. The system was built by laser engraving a manifold pattern on an acrylic block and sealing with another flat acrylic plate to form a microfluidic channel platform. The platform was incorporated with small solenoid valves to obtain a portable setup for programmable control of the liquid flow into the channel according to the HSI principle. The system was demonstrated for the determination of phosphate using a molybdenum blue method. An ascorbic acid, standard or sample, and acidic molybdate solutions were sequentially aspirated to fill the channel forming a stack zone before flowing to the detector. Under the optimum condition, a linear calibration graph in the range of 0.1–6 mg P L−1was obtained. The detection limit was 0.1 mg L−1. The system is compact (5.0 mm thick, 80 mm wide × 140 mm long), durable, portable, cost-effective, and consumes little amount of chemicals (83 μL each of molybdate and ascorbic acid, 133 μL of the sample solution and 1.7 mL of water carrier/run). It was applied for the determination of phosphate content in extracted soil samples. The percent recoveries of the analysis were obtained in the range of 91.2–107.3. The results obtained agreed well with those of the batch spectrophotometric method.en_US
dc.subjectChemistryen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleExploiting an automated microfluidic hydrodynamic sequential injection system for determination of phosphateen_US
dc.typeJournalen_US
article.title.sourcetitleTalantaen_US
article.volume177en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUbon Rajathanee Universityen_US
article.stream.affiliationsXavier Universityen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.