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Ho Li Ngee
Preferred name
Ho Li Ngee
Official Name
Ho, Li Ngee
Alternative Name
Li Ngee, Ho
Ho, Li Ngee
Ngee, Ho Li
Ho, L. N.
Main Affiliation
Scopus Author ID
57219028372
Researcher ID
DDY-6348-2022
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1 - 3 of 3
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PublicationHybrid system of photocatalytic fuel cell and Fenton process for electricity generation and degradation of Reactive Black 5( 2017-01-01)
;Noradiba Nordin ; ; ; ; ;Lee Sin Li ;Oon Yoong SinOon Yoong LingA novel hybrid system composed of a photocatalytic fuel cell (PFC) and Fenton reactor was developed with the aim to degrade the azo dye Reactive Black 5 (RB5) and generate electricity. Compared to previously established system of bioelectro-Fenton system, microbial fuel cell (MFC) system has significant challenge in the development and operation system. Therefore, PFC is used instead of MFC to generate electrons for the Fenton system. The effect of azo dye (RB5) on each PFC and Fenton reactor was investigated. The experimental results showed that maximum power output was achieved in the absence of dye in the Fenton reactor of this hybrid system. Furthermore, higher degradation efficiency of RB5 could also be observed in the PFC reactor in this hybrid system. -
PublicationUVA-irradiated dual photoanodes and dual cathodes photocatalytic fuel cell: Mechanisms and Reactive Red 120 degradation pathways( 2022-11-01)
;Ong Yong Por ; ; ; ; ;Thor Shen Hui ;Lee Sin LiTeoh Tean PengTo enhance dye removal and energy recovery efficiencies in single-pair electrode photocatalytic fuel cell (PFC-AC), dual cathodes PFC (PFC-ACC) and dual photoanodes PFC (PFC-AAC) were established. Results revealed that PFC-AAC yielded the highest decolorization rate (1.44 h−1) due to the promotion of active species such as superoxide radical (•O2−) and hydroxyl radical (•OH) when the number of photoanode was doubled. The results from scavenging test and UV-Vis spectrophotometry disclosed that •OH was the primary active species in dye degradation of PFC. Additionally, PFC-AAC also exhibited the highest power output (17.99 μW) but the experimental power output was much lower than the theoretical power output (28.24 μW) due to the strong competition of electron donors of doubled photoanodes to electron acceptors at the single cathode and its high internal resistance. Besides, it was found that the increments of dye volume and initial dye concentration decreased the decolorization rate but increased the power output due to the higher amount of sacrificial agents presented in PFC. Based on the abovementioned findings and the respective dye intermediate products identified from gas chromatography-mass spectrometry (GC-MS), the possible degradation pathway of RR120 was scrutinized and proposed.1 31 -
PublicationIntegrated photocatalytic and sequencing batch reactor (SBR) treatment system for degradation of phenol( 2017-04-06)
;Nik Noor Athirah Nik Yusoff ; ; ; ;Wan Fadhilah Wan Mohd KhalikLee Sin LiThis study will examine the efficiency of the simultaneous photocatalytic and biodegradation process in the same treatment reactor. The sequencing batch reactor or also known as SBR is an effective wastewater treatment method that has been applied widely. SBR system has become an alternative method for industrial wastewater treatment with high concentration of chemical oxygen demand (COD), and phenolic compound. In order for the photocatalytic process to occur, ZnO nanoparticles immobilized onto sponge were introduced to the reactor. It was observed that the COD value were decreased, indicated that the simultaneous biodegradation and photodegradation process in functional. The effect of ZnO nanoparticles on the production and composition of extracellular polymeric substances (EPS) and the physiochemical stability of activated sludge in hybrid growth type SBR were monitored. The percentages of removal are varied with different concentration of ZnO nanoparticles. The highest COD removal recorded is 31.5% with concentration of ZnO 0.6 mg/L. With the present of the ZnO nanoparticles, the degradation of phenol was relatively better than combination of biological of photlysis and biological.26 1