Wongwiriyapan, Winadda
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Preferred name
Wongwiriyapan, Winadda
Alternative Name
Wongwiriyapan, W.
Main Affiliation
Email
winadda.wo@kmitl.ac.th
11 results
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Item type:Publication, Investigation on electrochemical properties of sugarcane leaves-derived activated carbon by steam activation(2020-01-01) ;Ukkakimapan, Pundita ;Ukakimaparn, Prapart ;Wanchaem, Thanthamrong ;Yordsri, VisittapongSattayarut, VichudaSugarcane leaves (SLs) are a bio-waste from sugar production industry. To explore the value-added SLs, the SLs were used raw materials of activated carbons (ACs) by steam activation and their electrochemial properties were investigated for supercapacitor applications. The synthesis of ACs from the SLs consisted of two steps; carbonization at 500ºC and steam activation. The synthesis condition was optimized by varying activation temperature (800 and 850ºC) The porous structures were thoroughly formed on the surface after steam activation and the surface areas were reached to 630 and 639 m<sup>2</sup> g<sup>-1</sup> at the activation temperature of 800 and 850ºC, respectively. The SLs-derived ACs activated at 800ºC assembled in coin cell using organic electrolyte showed the highest specific capacitance of approximately 16 F g<sup>-1</sup> with a capacitance retention of 62% when the current density increased to 1.5 A g<sup>-1</sup>. Even though there is a room to improve the electrochemical properties such as optimization of porosity and removal of inorganic component, the SLs show a potential use as raw materials of ACs for supercapacitor applications. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, A flexible formaldehyde sensor based on palladium nanoparticles-polyvinylpyrrolidone-carbon nanotubes-nanocellulose composite films(2025-01-01) ;Chobsilp, Thanattha ;Muangrat, Worawut ;Inpaeng, Saowaluk ;Tedsree, KarakedYordsri, VisittapongA flexible formaldehyde sensor with high sensitivity was successfully fabricated by integrating palladium (Pd) nanoparticles, polyvinylpyrrolidone (PVP), multi-walled carbon nanotubes (MWCNTs) and nanocellulose (NC) into composite films. The flexible composite films were fabricated via vacuum filtration. The morphology, structure, composition, crystallinity, and functional group of as-fabricated sensing materials were characterized by scanning electron microscopy, transmission electron microscopy, electron probe microanalyzer, Raman spectroscopy, and Fourier transform infrared spectrometer. Pd nanoparticles-PVP-MWCNTs-NC (Pd-PVP-MWCNTs-NC) composite films exhibited an 11-fold increase in formaldehyde sensitivity compared to MWCNTs-NC composite films. The excellent sensing performances of Pd-PVP-MWCNTs-NC sensors were attributed to the combination of Pd nanoparticles and PVP. The enhanced sensitivity is attributed to the synergistic effect of the high electron transfer from formaldehyde molecule to Pd nanoparticles and swelling of PVP due to sorption of formaldehyde molecule. Pd-PVP-MWCNTs-NC sensors still maintained good response under bending angle up to 30° and 300 bending cycles. The results demonstrate that the Pd-PVP-MWCNTs-NC composite films are highly promising in terms of sensitivity and flexibility for sub-ppm level formaldehyde detection at room temperature. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Preparation of activated carbon via acidic dehydration of durian husk for supercapacitor applications(2020-08-01) ;Ukkakimapan, Pundita ;Sattayarut, Vichuda ;Wanchaem, Thanthamrong ;Yordsri, VisittapongPhonyiem, MayureeIn this study, the preparation of activated carbons (ACs) via acidic dehydration of durian husk (DH) for supercapacitor application was investigated. The DH was dehydrated using sulfuric acid and subsequently activated by using sodium hydroxide as chemical reagent at 720 °C to obtain activated carbon (hereinafter referred to as DA). Surpassing the commercial ACs and the ACs derived from the conventional carbonization and activation (hereinafter referred to as CA), the DA exhibited superior properties in high surface area (2578 m<sup>2</sup>/g) and total pore volume (1.27 cm<sup>3</sup>/g). Moreover, besides carbon and oxygen, the DA contained sulfur and nitrogen in the carbon network. The DA can act as a suitable material for supercapacitor electrode with the specific gravimetric and volumetric capacitances of 145 F/g and 70 F/cm<sup>3</sup> in an organic electrolyte. The device also showed a promising performance with an energy density of 32 Wh/kg and a power density of 316 W/kg. These results demonstrate that the preparation of ACs via acidic dehydration of DH offers the advantages in terms of simplicity, low cost, and short-time processing to achieve heteroatom self-doped ACs with a high surface area for high-performance supercapacitors. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Hemp-Derived Hierarchical Porous Carbon with an Optimized Pore Structure by NaOH Activation for Supercapacitor Applications(2025-11-11) ;Bowornthommatadsana, Khemjiranee ;Klangvijit, Kanisorn ;Uwanno, Teerayut ;Phonyiem Reilly, MayureeYordsri, VisittapongThis study focuses on converting hemp hurd, a byproduct of hemp stalk processing, into high-performance activated carbon for supercapacitor applications. Hemp hurd was pyrolyzed and subsequently activated with NaOH at various ratios (biochar:NaOH = 1:1, 1:2, 1:3, 1:4). The Hurd-4 condition (1:4 ratio) yielded the highest specific surface area, 3033 m<sup>2</sup>/g. Our findings indicate that increasing the chemical activation ratio enhances the mesopore-to-micropore volume ratio (V<inf>meso</inf>/V<inf>micro</inf>) to 1.58 while maintaining a sufficient micropore volume for ion storage. This balanced pore structure effectively increased the specific capacitance, achieving a maximum of 725 F/g at a current density of 0.3 A/g in a 1 M H<inf>2</inf>SO<inf>4</inf>electrolyte. When assembled into a coin cell with an organic electrolyte, Hurd-4 exhibited a maximum specific capacitance of 39 F/g, a maximum energy density of 34 Wh/kg, and a power density of 395 W/kg, surpassing commercial activated carbon. Additionally, the device maintained 78% capacitance retention after 10,000 cycles at a current density of 0.5 A/g. The superior electrochemical properties are attributed to the largest specific surface area, highest pore volume, and optimal mesopore volume ratio. These results demonstrate the potential of hemp hurd as a highly efficient precursor for synthesizing activated carbon for high-performance supercapacitors. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Optimizing Electrochemical Performance: A Study of Aqueous Electrolytes with Hemp-Derived Activated Carbon for Supercapacitors(2025-02-25) ;Klangvijit, Kanisorn ;Bowornthommatadsana, Khemjiranee ;Phonyiem Reilly, Mayuree ;Uwanno, TeerayutYordsri, VisittapongThis work investigates the synthesis and electrochemical performance of hemp-derived activated carbon (HAC) for supercapacitor electrode applications. HAC was prepared through NaOH chemical activation, and its electrochemical characteristics were evaluated using three different electrolytes: acidic (H<inf>2</inf>SO<inf>4</inf>), neutral (Na<inf>2</inf>SO<inf>4</inf>), and basic (KOH). The specific surface area of HAC was found to be exceptionally high, measuring 2612 m<sup>2</sup>/g, surpassing that of commercially available activated carbon (AC). Surface analysis revealed the presence of an oxygen functional group, which provided additional pseudocapacitive active sites. When 1 M H<inf>2</inf>SO<inf>4</inf> was employed as the electrolyte, HAC demonstrated a maximum specific capacitance of 594 F/g (302.4 F/cm<sup>3</sup>) at a current density of 0.3 A/g. Notably, the HAC electrode exhibited significantly higher energy density and power density, reaching values of 82 Wh/kg (135.7 mWh/cm<sup>3</sup>) and 188 W/kg (311 mW/cm<sup>3</sup>), respectively, when compared to commercial AC. These results highlight the potential of HAC as a cost-effective and high-performance electrode material, particularly when paired with H<inf>2</inf>SO<inf>4</inf> as the electrolyte due to their ideal micropore/mesopore ratio for H<inf>2</inf>SO<inf>4</inf> electrolyte access. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Effect of Carbonization Temperature on Physical Properties and Specific Capacitance of Activated Carbon Derived from Banana Stem and Its Application as Supercapacitor Electrodes(2023-01-01) ;Dulyaseree, Paweena ;Sama, Hasanee ;Sada, Suraida ;Ukkakimapan, PunditaYordsri, VisittapongIn this work, activated carbons (ACs) for electrodes supercapacitor applications were successfully synthesized from banana stem. Banana is one of the popular fruits that is easy to grow and most parts of the plant can be used. However, banana cultivation generates a lot of wastes, especially from the stem. Thus, using banana stem as raw material for ACs was investigated. The synthesis of AC consisted of 2 processes; carbonization and activation. The advantage of a two-step synthesis was the low weight loss of charcoal. Firstly, the carbonization process was conducted by varying the temperature between 300-600°C, and then inorganic elements were removed by treatment with 1 M sulfuric acid. After that, activation was conducted at 720°C under an argon atmosphere. The electrochemical properties of banana stem-derived ACs (BCH-ACs) were studied using sodium sulfate as an electrolyte. The BCH-ACs carbonized at 400°C showed the highest performance with a specific capacitance of 55.45 Fg<sup>-1</sup>, an energy density of 7.70 Whkg<sup>-1</sup> and a power density of 133.94 Wkg-1. The highest specific capacitance of the BCH400-AC was likely due to the increase in the amount of oxygenated functional group, which facilitated the access of electrolyte ions into the electrode. These results suggest that banana stem can be used to synthesize ACs via carbonization at 400°C, and the ACs generated can be applied as electrode in supercapacitors. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Band gap and photo charge carrier tailoring in zirconium doped carbon nitride using ZrCl4-DMF-melamine for photocatalytic degradation of rhodamine B(2025-03-05) ;Pinming, Chinathun ;Yang, Qingshan; ;Yordsri, VisittapongImproving the performance of carbon nitride (CN) photocatalysts in photocatalytic degradation applications involves optimizing their morphology, electronic properties, and optical characteristics. Zirconium-doped carbon nitride (Zr-doped CN) photocatalysts were synthesized using dimethylformamide (DMF) as a solvent to facilitate the formation of complex molecular structures for effective metal doping. By varying the concentration of the zirconium tetrachloride (ZrCl<inf>4</inf>) precursor between 1 and 3 mmol, we observed significant enhancements in photocatalytic activity. Notably, controlling the ZrCl<inf>4</inf> concentration below 3 mmol prevented the formation of zirconium oxide phases, which could otherwise negatively affect the photocatalytic performance. Zr incorporation led to the morphological transformation of CN from a bulk structure into a hierarchical porous structure, increasing the surface area to 135 m<sup>2</sup> g<sup>−1</sup>. Additionally, Zr doping changed the band energy and electronic properties, creating an optimal energy level for generating oxygen radicals in the photocatalytic water-splitting processes. The photocatalytic degradation of rhodamine B showed that the Zr-doped CN photocatalysts achieved 4.5-fold better performance than undoped CN. Moreover, a small amount of ethylenediaminetetraacetic acid (EDTA) significantly enhanced the photocatalytic efficiency of Zr-doped CN compared to that of undoped CN. These results indicate that combining Zr-doped CN with other materials to create Z-scheme or S-scheme structures could further enhance its performance, thus emphasizing the potential of increasing photocatalytic efficiency by optimizing energy band structures and forming heterostructured photocatalysts. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Preparation of Chitin Nanofibers and Natural Rubber Composites and Their Triboelectric Nanogenerator Applications(2024-02-01) ;Petchnui, Kattaliya ;Uwanno, Teerayut ;Phonyiem Reilly, Mayuree ;Pinming, ChinathunTreetong, AlongkotTriboelectric nanogenerators (TENGs) have gained significant attention as promising energy-harvesting devices that convert mechanical energy into electrical energy through charge separation induced by friction and electrostatic induction. In this study, we explore the utilization of biowaste shrimp shell-extracted chitin nanofiber (ChNF) as a viable eco-friendly material for TENG applications. Composite materials were prepared by incorporating ChNF into natural rubber (NRL) at loading levels of 0.1 and 0.2 wt% (NRL/ChNF) to form the TENG triboelectric layer. ChNFs with a uniform width of approximately 10–20 nm were successfully extracted from the shrimp shells through a simple mechanical procedure. The NRL/ChNF composites exhibited enhanced mechanical properties, as evidenced by a higher Young’s modulus (3.4 GPa) compared to pure NRL. Additionally, the NRL/ChNF composites demonstrated an increased dielectric constant of 3.3 at 0.1 MHz. Moreover, the surface potential difference of NRL increased from 0.182 V to 1.987 V in the NRL/ChNF composite. When employed as the triboelectric layer in TENG, the NRL/ChNF composites exhibited significant improvement in their output voltage, with it reaching 106.04 ± 2.3 V. This enhancement can be attributed to the increased dielectric constant of NRL/ChNF, leading to enhanced charge exchange and charge density. This study presents a straightforward and environmentally friendly technique for preparing sustainable natural materials suitable for energy-harvesting devices. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Surface Modification of Activated Carbon by Nitrogen Doping and KOH Activation for Enhanced Carbon Dioxide Adsorption Performance(2025-01-01) ;Chobsilp, Thanattha ;Treetong, Alongkot ;Yordsri, Visittapong ;Santasnachok, MattanaCharoeythornkhajhornchai, PollawatNitrogen-doped activated carbon (N-AC) was successfully prepared by KOH-activation and nitrogen doping using ammonia (NH<inf>3</inf>) heat treatment. Coconut shell-derived activated carbon (AC) was heat-treated under NH<inf>3</inf> gas in the temperature range of 700℃–900℃. Likewise, the mixture of potassium hydroxide (KOH) and AC was heated at 800℃, followed by heat treatment under NH<inf>3</inf> gas at 800℃ (hereafter referred to as KOH-N-AC800). Scanning electron microscopy (SEM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) method were utilized to analyze morphology, crystallinity, chemical bonding, chemical composition and surface area. The surface area and porosity of N-AC increased with increasing NH<inf>3</inf> heat treatment. Similarly, the nitrogen content in the N-AC increased from 3.23% to 4.84 at% when the NH<inf>3</inf> heat treatment was raised from 700℃ to 800℃. However, the nitrogen content of N-AC decreased to 3.40 at% after using NH<inf>3</inf> heat treatment at 900℃. The nitrogen content of KOH-N-AC800 is 5.43 at%. KOH-N-AC800 and N-AC800 exhibited improvements of 33.66% and 26.24%, respectively, in CO<inf>2</inf> adsorption compared with AC. The enhancement of CO<inf>2</inf> adsorption of KOH-N-AC800 is attributed to the synergic effect of the nitrogen doping, high surface area, and porosity. The results exhibited that nitrogen sites on the surface play a more significant role in CO<inf>2</inf> adsorption than surface area and porosity. This work proposes the potential synergistic effect of KOH-activation and nitrogen doping for enhancing the CO<inf>2</inf> adsorption capacity of activated carbon. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Synergistic effect of nickel nanoparticles and carbon nanotubes buckypaper for enhancement of microwave shielding properties(2020-01-01) ;Sukgorn, Nuttaya ;Yordsri, Visittapong ;Thanachayanon, Chanchana ;Horprathum, MatiChudpooti, NonchanuttCarbon nanotubes (CNTs) are considered as the most promising materials to solve the electromagnetic interference (EMI) issue. Various forms of CNTs including CNTs/polymer composites, metal nanoparticles-decorated CNTs and freestanding CNT buckypapers (CNT BPs) have been proposed to enhance shielding effectiveness. In this study, the synergistic effect of nickel nanoparticles (NPs) and relatively short CNTs for the enhancement of microwave shielding properties was investigated. CNT BPs were prepared by vacuum filtration of well-dispersed multi-walled CNTs and subsequently nickel was decorated on the CNT BPs (Ni/CNT) by pulsed DC sputtering technique with different deposition times of 0, 5, 10 and 15 min (hereinafter referred to as CNi0, CNi05, CNi10 and CNi15, respectively). The diameter of Ni/CNT increased from 8.74±0.53 to 72.5±3.2 nm and the conductivity improved from 9.57±0.87 to 12.57±0.59 S/cm when the nickel deposition time was 15 min. Nickel NPs were the mixed phases of nickel and nickel oxide with a dominant nickel phase. The shielding effectiveness at the frequency of 9.5 GHz achieved to-34.1 dB for CNi15. The enhancement of shielding effectiveness of CNi15 is attributed to the synergistic effect of CNTs and nickel NPs on wave dissipation.
