Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12995
Title: Novel colorimetric assay for paraquat detection on-silica bead using negatively charged silver nanoparticles
Authors: Siangproh W.
Somboonsuk T.
Chailapakul O.
Songsrirote K.
Keywords: Color
Colorimeters
Colorimetry
Groundwater
Metal nanoparticles
Silica
Silica gel
Silver nanoparticles
Synthesis (chemical)
Coulombic attractions
Direct determination
Extraction procedure
Nanopaticles
Optical detection
Paraquat
Silica beads
Silver nanoparticles (AgNps)
Herbicides
metal nanoparticle
microsphere
paraquat
silicon dioxide
silver
water
Brassica rapa
chemistry
colorimetry
limit of detection
procedures
Brassica rapa
Colorimetry
Limit of Detection
Metal Nanoparticles
Microspheres
Paraquat
Silicon Dioxide
Silver
Water
Issue Date: 2017
Abstract: A simple, rapid, sensitive, and economical method based on colorimetry for the determination of paraquat, a widely used herbicide, was developed. Citrate-coated silver nanoparticles (AgNPs) were synthesized as the colorimetric probe. The mechanism of the assay is related to the aggregation of negatively charged AgNPs as induced by positively-charged paraquat resulting from coulombic attraction which causes the color to change from a deep greenish yellow to pale yellow in accordance with the concentrations of paraquat. Silica gel was exploited as the paraquat adsorbent for purification and pre-concentration prior to the direct determination with negatively charged AgNPs without the requirement of the elution step. The validity of the proposed approach was evaluated by spiking standard paraquat in water and plant samples. Recoveries of paraquat in water samples were 93.6% and 95.4% for groundwater and canal water, respectively, while those in plant samples were 89.5% and 86.6% for Chinese cabbage and green apple, respectively,after using the optimized extraction procedure. The absorbance of AgNPs at 400 nm was linearly related to the concentration of paraquat over the range of 0.05–50 mg L−1, with detection limits of 0.05 mg L−1 for water samples, and 0.10 mg L−1 for plant samples by naked eye determination. © 2017 Elsevier B.V.
URI: https://ir.swu.ac.th/jspui/handle/123456789/12995
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021165709&doi=10.1016%2fj.talanta.2017.06.045&partnerID=40&md5=6be50544e71f45e130649afbe54abc37
ISSN: 399140
Appears in Collections:Scopus 1983-2021

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