Areerob, Yonrapach

Preferred name

Areerob, Yonrapach

Main Affiliation

School of Engineering

yonrapach.ar@kmitl.ac.th

Now showing 1 - 6 of 6

Some of the metrics are blocked by your
consent settings
Novel gamma-irradiated chitosan-doped reduced graphene-CuInS2 composites as counter electrodes for dye-sensitized solar cells
(2022-05-20)
Areerob, Yonrapach
;
Hamontree, Chaowalit
;
Sricharoen, Phitchan
;
Limchoowong, Nunticha
;
Laksee, Sakchai
To address the issues associated with traditional counter electrodes, a novel gamma-irradiated chitosan-doped reduced graphene-CuInS<inf>2</inf> composite (Chi@RGO-CIS) was used as the counter electrode (CE). The system was fabricated following a simple hydrothermal method. The prepared Chi@RGO-CIS was characterized by various spectroscopic and microscopic techniques. The synergistic effect between chitosan, CuInS<inf>2</inf>, and reduced graphene oxide can help in producing a large surface area. It can also help in the generation of catalytic sites toward I-/I<inf>3</inf>-redox electrolytes. We used a composite (based on electrical considerations) to study the effect of the amount of graphene on the characteristics and photovoltaic efficiency of the Chi@RGO-CIS composites. The solar cell assembled with 1.5% Chi@RGO-CIS exhibited an efficiency of 12.21%. The efficiency was higher than that of a Pt-based device (9.96%) fabricated under the same conditions. Hence, Chi@RGO-CIS can be potentially used as the CE of dye-sensitized solar cells (DSSCs). It can be used as a substitute for Pt in DSSCs.
Some of the metrics are blocked by your
consent settings
Selective Fe(ii)-fluorescence sensor with validated two-consecutive working range using N,S,I-GQDs associated with garlic extract as an auxiliary green chelating agent
(2022-05-12)
Pimsin, Nipaporn
;
Keawprom, Chayanee
;
Areerob, Yonrapach
;
Limchoowong, Nunticha
;
Sricharoen, Phitchan
The goal of this work was to use the pyrolysis process to synthesize graphene quantum dots doped with garlic extract (as N,S-GQDs) and simultaneously co-doped with iodine (as I-GQDs). XPS, HR-TEM, FE-SEM/EDX, FT-IR, fluorescence, and UV-visible absorption spectroscopy were used to characterize the N,S,I-GQDs and analyze their morphological images. The quantum yield of N,S,I-GQDs was found to be 45%, greater than that of undoped GQDs (31%). When stimulated at 363 nm, the N,S,I-GQDs display a strong fluorescence intensity at a maximum wavelength of 454 nm. Using N,S,I-GQDs as a fluorescence quenching sensor for screening tests with various metal ions, it was discovered that they are extremely selective towards Fe2+ over Fe3+ and other ions. Thus, solution pH, concentration of N,S,I-GQDs, quantity of garlic extract, EDTA and AgNO<inf>3</inf> concentration as masking agents, reaction duration under ultrasonic aid, and tolerable limit of Fe3+ presence in the target analyte were all optimized for Fe2+ detection. A highly sensitive detection of Fe2+ was obtained using a linear curve with y = 141.34x + 5.5855, R2 = 0.9961, LOD = 0.11 mg L−1, and LOQ = 0.35 mg L−1. The method precision, given as RSDs, was determined to be satisfactory at 1.04% for intra-day analysis and 3.22% for inter-day analysis, respectively. As a result, the selective determination of trace amounts of Fe2+ in real water samples using such labile multi-element doped GQDs in conjunction with garlic extract as a green chelating agent to maintain its enhanced sensitivity was successfully applied with good recoveries ranging from 89.16 to 121.45%.
Some of the metrics are blocked by your
consent settings
A Fluorescence Switching Sensor for Sensitive and Selective Detections of Cyanide and Ferricyanide Using Mercuric Cation-Graphene Quantum Dots
(2021-06-08)
Kongsanan, Niradchada
;
Pimsin, Nipaporn
;
Keawprom, Chayanee
;
Sricharoen, Phitchan
;
Areerob, Yonrapach
This study aims to use graphene quantum dots (GQDs) as a fluorescence switching sensor (turn on-off) for the simultaneous detection of cyanide (CN-) and ferricyanide [Fe(CN)6]3- in wastewater samples. The GQDs were synthesized by pyrolyzing solid citric acid. The intrinsic blue color of the solution was observed under ultraviolet irradiation. The fluorescence spectrum was maximized at both excitation and emission wavelengths of 370 and 460 nm, respectively. The fluorescence intensity of GQDs decorated with Hg2+ (turn-off mode as the starting baseline) could be selectively turned on in the presence of CN- and once back to turn-off mode by [Fe(CN)6]3-. The fluorescence switching properties were used to develop a fluorescence turn-on-off sensor that could be used to detect trace amounts of CN- and [Fe(CN)6]3- in water samples. For highly sensitive detection under optimum conditions (Britton-Robinson buffer solution in the pH range of 8.0-9.0, linearity ranges of 5.0-15.0 μM (R2 = 0.9976) and 10.0-50.0 μM (R2 = 0.9994), respectively, and detection limits of 3.10 and 9.48 μM, respectively), good recoveries in the ranges of 85.89-112.66% and 84.88-113.92% for CN- and [Fe(CN)6]3-, respectively, were recorded. The developed methods were successfully used for the simultaneous and selective detection of CN- and [Fe(CN)6]3- in wastewater samples obtained from local municipal water reservoirs.
Some of the metrics are blocked by your
consent settings
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
(2021-06-15)
Pimsin, Nipaporn
;
Kongsanan, Niradchada
;
Keawprom, Chayanee
;
Sricharoen, Phitchan
;
Nuengmatcha, Prawit
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.
Some of the metrics are blocked by your
consent settings
Synthesis of novel MoWO4 with ZnO nanoflowers on multi-walled carbon nanotubes for counter electrode application in dye-sensitized solar cells
(2022-12-01)
Areerob, Yonrapach
;
Hamontree, Chaowalit
;
Sricharoen, Phitchan
;
Limchoowong, Nunticha
;
Nijpanich, Supinya
Novel MoWO<inf>4</inf> with ZnO nanoflowers was synthesized on multi-walled carbon nanotubes (MW-Z@MWCNTs) through a simple hydrothermal method, and this unique structure was applied as a counter electrode (CE) for dye-sensitized solar cells (DSSC) for the first time. The synergetic effect of ZnO nanoflowers and MoWO<inf>4</inf> on MWCNTs was systematically investigated by different techniques. The amount of MWCNTs was optimized to achieve the best DSSC performance. It was found that the 1.5% MW-Z@MWCNTs composite structure had the highest power conversion efficiency of 9.96%, which is greater than that of traditional Pt CE. Therefore, MW-Z@MWCNTs-based CE can be used to replace traditional Pt-based electrodes in the future.
Some of the metrics are blocked by your
consent settings
Ultrasound-irradiated synthesis of 3-mercaptopropyl trimethoxysilane-modified hydroxyapatite derived from fish-scale residues followed by ultrasound-assisted organic dyes removal
(2021-12-01)
Sricharoen, Phitchan
;
Kongsri, Supalak
;
Kukusamude, Chunyapuk
;
Areerob, Yonrapach
;
Nuengmatcha, Prawit
We report a novel method for the synthesis of 3-mercaptopropyl trimethoxysilane-modified hydroxyapatite (FHAP-SH) derived from fish-scale residues by using ultrasound irradiation. Scanning electron microscopy, transmission electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy were used for the FHAP-SH characterization. Then, the organic dye adsorption on the FHAP-SH was monitored through an ultrasound process. After the dye removal optimization, significant improvements were observed in the maximum adsorption capacities for Congo Red (CR, 500 mg g−1), Coomassie Brilliant Blue G 250 (CB, 235 mg g−1), and Malachite Green (MG, 625 mg g−1). The adsorption behaviors of these dyes were fitted by using the Langmuir isotherm model with a high coefficient of determination values ranging from 0.9985 to 0.9969. The adsorption of the three dyes onto FHAP-SH was an endothermic process based on the adsorption thermodynamics model, while the adsorption kinetics analysis of the dyes presented a good alignment with the pseudo-second-order kinetics. The FHAP-SH exhibits a remarkably high adsorption capacity, is inexpensive, and fulfills the ecofriendly requirements of dye wastewater treatment, especially in the textile industry.

Areerob, Yonrapach

Filters

Settings

Sort By

Results per page