Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17259
Title: Ultratrace Detection of Nickel(II) Ions in Water Samples Using Dimethylglyoxime-Doped GQDs as the Induced Metal Complex Nanoparticles by a Resonance Light Scattering Sensor
Authors: Pimsin N.
Kongsanan N.
Keawprom C.
Sricharoen P.
Nuengmatcha P.
Oh W.-C.
Areerob Y.
Chanthai S.
Limchoowong N.
Issue Date: 2021
Abstract: This study aimed to synthesize dimethylglyoxime (DMG) (N-source)-doped graphene quantum dots (N-GQDs) via simultaneous pyrolysis of citric acid and 1.0% (w/v) DMG. The maximum excitation wavelength (λmax, ex = 380 nm) of the N-GQD solution (49% quantum yield (QY)) was a red shift with respect to that of bare GQDs (λmax, ex = 365 nm) (46% QY); at the same maximum emission wavelength (λmax, em = 460 nm), their resonance light scattering (RLS) intensity peak was observed at λmax, ex/em = 530/533 nm. FTIR, X-ray photoelectron spectroscopy, XRD, energy-dispersive X-ray spectroscopy, and transmission electron microscopy analyses were performed to examine the synthesized materials. The selective and sensitive detection of Ni2+ using the RLS intensity was performed at 533 nm under the optimum conditions consisting of both 25 mg L-1 N-GQDs and 2.5 mg L-1 DMG in the ammonium buffer solution of pH 9.0. The linearity of Ni2+ was 50.0-200.0 μg L-1 with a regression line, y = 5.031x - 190.4 (r2 = 0.9948). The limit of detection (LOD) and the limit of quantitation (LOQ) were determined to be 20.0 and 60.0 μg L-1, respectively. The method precision expressed as % RSDs was 4.90 for intraday (n = 3 × 3) and 7.65 for interday (n = 5 × 3). This developed method afforded good recoveries of Ni2+ in a range of 85-108% when spiked with real water samples. Overall, this innovative method illustrated the identification and detection of Ni2+ as a DMG complex with N-GQDs, and the detection was highly sensitive and selective. ©
URI: https://ir.swu.ac.th/jspui/handle/123456789/17259
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85108542297&doi=10.1021%2facsomega.1c00190&partnerID=40&md5=5718983ac1611fecd8af5870a1acc308
ISSN: 24701343
Appears in Collections:Scopus 1983-2021

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