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Dive into the research topics where Bor-Yann Chen is active.

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Featured researches published by Bor-Yann Chen.


Bioresource Technology | 2010

Assessment upon azo dye decolorization and bioelectricity generation by Proteus hauseri.

Bor-Yann Chen; Meng-Meng Zhang; Chang-Tang Chang; Yongtao Ding; Kae-Long Lin; Chyow-San Chiou; Chung-Chuan Hsueh; Huizhong Xu

This study explored dye decolorization and bioelectricity generation of indigenous Proteus hauseri ZMd44 for dye-bearing wastewater treatment. Chemical structures of azo dyes apparently affected the performance of dye biodecolorization. Additions of diazo dye C.I. reactive blue 160 (RBu160) stimulated simultaneous dye decolorization and bioelectricity generation of ZMd44 in single chamber microbial fuel cells (MFCs). However, high-level additions of RBu160 repressed capabilities of power production in MFC due to competition of electrons used for reductive decolorization. Decolorized intermediates of RBu160-phenyl methadiamine and 5-sulfoanthranilic acid as electron shuttles might mediate electron transport for current generation in MFC.


Journal of Hazardous Materials | 2009

Understanding effects of chemical structure on azo dye decolorization characteristics by Aeromonas hydrophila

Chung-Chuan Hsueh; Bor-Yann Chen; Chia-Yi Yen

This novel comparative study tended to disclose how the molecular structures present in seven azo dyes including two types of azo dyes (i.e., naphthol type azo dyes--Reactive Black 5 (RB 5), Reactive Blue 171 (RB 171), Reactive Green 19 (RG19), Reactive Red 198 (RR198), Reactive Red 141 (RR141), and non-naphthol type azo dyes--Direct Yellow 86 (DY86), Reactive Yellow 84 (RY84)) affected color removal capability of Aeromonas hydrophila. Generally speaking, the decolorization rate of naphthol type azo dye with hydroxyl group at ortho to azo bond was faster than that of non-naphthol type azo dye without hydroxyl group, except of RG19. The azo dyes with electron-withdrawing groups (e.g., sulfo group in RR198, RB5 and RR141) would be easier to be decolorized than the azo dyes with the electron-releasing groups (e.g., -NH-triazine in RB171 and RG19). In addition, the azo dyes containing more electron-withdrawing groups (e.g., RR198, RB5 and RR141) showed significantly faster rate of decolorization. The azo dyes with electron-withdrawing groups (e.g., sulfo group) at para and ortho to azo bond (e.g., RR198, RB5 and RR141) could be more preferred for color removal than those at meta (e.g., DY86 and RY84). The former azo dyes with para and ortho sulfo group provided more effective resonance effects to withdraw electrons from azo bond, causing azo dyes to be highly electrophilic for faster rates of reductive biodecolorization. However, since the ortho substituent caused steric hindrance near azo linkage(s), azo dyes with para substituent could be more favorable (e.g., SO(2)(CH(2))(2)SO(4)(-) in RR198 and RB5) than those with ortho substituent (e.g., sulfo group at RR141) for decolorization. Thus, the ranking of the position for the electron-withdrawing substituent in azo dyes to escalate decolorization was para>ortho>meta. This study suggested that both the positions of substituents on the aromatic ring and the electronic characteristics of substituents in azo dyes all significantly affected the performance of biodecolorization of A. hydrophila.


Bioresource Technology | 2010

Comparative study on characteristics of azo dye decolorization by indigenous decolorizers.

Meng-Meng Zhang; Wen-Ming Chen; Bor-Yann Chen; Chang-Tang Chang; Chung-Chuan Hsueh; Yongtao Ding; Kae-Long Lin; Huizhong Xu

This study provides a first attempt to explore indigenous strains with excellent decolorization capability from the most biodiverse region in Taiwan for dye-bearing wastewater treatment. Bacterial isolates were obtained via serial selections under selection pressure of the fungicide nystatin and model textile dye(s). According to profiles of protein expression and PCR-augmented 16S rRNA gene analyses for strain identification, >99% of nucleotide sequences in isolated strains were identical to type strains Aeromonas hydrophila, Klebsiella pneumoniae, Enterobacter cancerogenus, Proteus hauseri, Acinetobacter johnsonii. This first-attempt study not only explored most abundant decolorizers in Taiwan, but also compared their color removal performance for further applications.


Journal of Environmental Sciences-china | 2011

Application of magnetic particles modified with amino groups to adsorb copper ions in aqueous solution

Ya-Fen Lin; Hua-Wei Chen; Kae-Long Lin; Bor-Yann Chen; Chyowsan Chiou

A magnetic adsorbent can be easily recovered from treated water by magnetic force, without requiring further downstream treatment. In this research, amine-functionalized silica magnetite has been synthesized using N-[3-(trimethoxysilyl)propyl]-ethylenediamine (TPED) as a surface modification agent. The synthesized magnetic amine adsorbents were used to adsorb copper ions in an aqueous solution in a batch system, and the maximum adsorption was found to occur at pH 5.5 +/- 0.1. The adsorption equilibrium data fitted the Langmuir isotherm equation reasonably well, with a maximum adsorption capacity of 10.41 mg/g. A pseudo second-order model could best describe the adsorption kinetics, and the derived activation energy was 26.92 kJ/mol. The optimum condition to desorb Cu2+ from NH2/SiO2/Fe3O4 was provided by a solution with 0.1 mol/L HNO3.


Bioresource Technology | 2011

Understanding interactive characteristics of bioelectricity generation and reductive decolorization using Proteus hauseri.

Bor-Yann Chen; Yu-Min Wang; I-Son Ng

This first-attempt study quantitatively explored interactive characteristics of bioelectricity generation and dye decolorization in air-cathode single-chamber microbial fuel cells (MFCs) using indigenous Proteus hauseri ZMd44. After approx. 15 cycles (30 days) acclimatization in dye-bearing cultures, P. hauseri could express its stable capability of simultaneous bioelectricity generation and color removal (SBP&CR) in MFCs. Evidently, appropriate acclimation strategy for formation of the electrochemically active anodic biofilm played a crucial role to enhance the performance of SBP&CR in MFCs. Gradually increased supplementations of C.I. reactive blue 160 resulted in progressively decreased decay rate of bioelectricity generation. That is, a dye decolorized in a faster rate would result in a lower capability for bioelectricity generation and vice versa. In addition, a reduced dye with less toxicity potency (e.g., 2-aminophenol) might work as a redox mediator of electron transport to anodic biofilm for bioelectricity generation in MFCs.


Journal of Hazardous Materials | 2009

Revealing interactive toxicity of aromatic amines to azo dye decolorizer Aeromonas hydrophila.

Bor-Yann Chen; Kai-Wei Lin; Yu-Min Wang; Chia-Yi Yen

This study attempted to combine chemostat pulse technique (CPT) and dose-mortality assessment in pursuit of quantitative rankings of toxicity of model aromatic amines (MAAs) in the presence of diazo dye reactive red 141 (or Evercion Red H-E7B; RR141) upon Aeromonas hydrophila. As known, bacterial decolorization performance of azo dyes is directly dependent upon both the characteristics of biochemical reactivity and biotoxicity of dyes and related aromatic amines towards color removal. Thus, the findings herein indicated that the relative toxicity series of MAAs were (1) ortho>para>MAA-free control>meta position (for isomeric aminophenols); (2) -OH>-SO(3)H>MAA-free control (-NH(2) at ortho position); (3) -COOH>MAA-free control>-OH (-NH(2) at meta position) through the CPT at 200mg/L MAAs. Comparison on results in higher levels of MAAs at 1000 mg/L almost showed parallel relative toxicity rankings at 200mg/L. Quantification using traditional plate count method also confirmed nearly similar trends for corresponding MAAs except 3-aminophenol, revealing the promising feasibility of CPT for the toxicity assessment in practical applications. In addition, dose-mortality analysis regularly used in toxicology was used to quantitatively determine toxicity rankings of MAAs. In conclusion, this study directly provided a kinetic model to quantify the relative toxicity ranking of MAAs in the presence of RR141. It could provide a feasible guideline for assessment on the toxicity or treatability of azo dyes and MAAs to A. hydrophila in wastewater treatment.


Journal of Bioscience and Bioengineering | 2012

Deciphering simultaneous bioelectricity generation and dye decolorization using Proteus hauseri

Bor-Yann Chen; Yu-Min Wang; I-Son Ng; Shi-Qi Liu; Jhao-Yin Hung

This first-attempt study disclosed how and why electron-shuttling mediators were capable to stimulate bioelectricity-generating capabilities of dye-bearing microbial fuel cells (MFCs) using Proteus hauseri. Due to significant biotoxicity of 4-aminophenol (4AP) and the absence of electron-mediating potential of 3AP, only 2AP among all isomers could work as an exogenous mediator to stimulate bioelectricity generation of P. hauseri. Dye toxicity to cells on anodic biofilm in MFCs apparently affected the performance of simultaneous bioelectricity production and color removal (SBP&CR) in MFCs. Plus, dose-response analysis upon toxicity potency of reactive blue 160 revealed that cells on anodic biofilm in MFCs had a higher tolerance to reactive blue 160 than suspended cells. Apparently, augmentation of electron mediator(s) with low toxicity was a feasible means to facilitate bioelectricity-generating capability of SBP&CR.


Bioresource Technology | 2013

Deciphering mediating characteristics of decolorized intermediates for reductive decolorization and bioelectricity generation.

Bor-Yann Chen; Chung-Chuan Hsueh; Shi-Qi Liu; I-Son Ng; Yu-Min Wang

As decolorized intermediates could play a role of electron-shuttling mediator to enhance the performance of dye decolorization and bioelectricity generation, this study selected model compounds with auxochromes (e.g., benzene-1,2-diol, 1,2-diaminobenzene) to explore how chemical structure(s) affected color removal and power producing capabilities in microbial fuel cells (MFCs). According to cyclic voltammetry, respiratory testing and MFC data, promising electron-shuttling capabilities of aforementioned compounds were revealed using Proteus hauseri ZMd44, Aeromonas sp. C78, Acinetobacter johnsonii NIUx72 bearing MFCs. These findings clearly indicated that chemical structure(s) of decolorized mediators directly affected characteristics of simultaneous reductive decolorization and bioelectricity generation in MFCs, suggesting feasible operation strategy of MFCs for industrial applications.


Journal of Hazardous Materials | 2009

Comparative assessment upon dye removal capability of indigenous bacterial strains from Lanyang Plain in northeast Taiwan.

Bor-Yann Chen; Wen-Ming Chen; Hsiang-Yin Kuo; Chung-Chuan Hsueh

This study provides a first attempt from a geological and ecological perspective to look forward isolations of indigenous strains with the decolorization capability from the most biodiverse region in Taiwan for dye-laden wastewater treatment. Serial selections were conducted by a specific use of the fungicide nystatin and model azo dye C.I. reactive red 141 (RR141) during isolation. Several bacterial strains with the excellent capability of azo dye decolorization were predominantly isolated from river water and mud samples of Lanyang River Basin. Phase-curve profiles indicated that azo dye decolorization was found to be non-growth associated for both mixed cultures and isolated pure strains. The color removal efficiency of the mixed culture was nearly 10-fold to that of Pseudomonas luteola at ca. 600mgL(-1) RR141, indicating a promising feasibility of isolated cultures to be applicable for practical treatments. The decolorization performance of unacclimated and acclimated pure cultures was at most 20% and 70-80% to that of the mixed cultures, respectively. It might suggest that combined interactions among decolorizers were crucial for the optimal color removal. According to the results of physiological and 16S rRNA gene sequence examinations, the isolated strains should belong to Aeromonas species (very likely A. hydrophila).


Waste Management & Research | 2010

Waste brick’s potential for use as a pozzolan in blended Portland cement

Kae-Long Lin; Bor-Yann Chen; Chyow-San Chiou; An Cheng

This study investigated the pozzolanic reactions and engineering properties of waste brick-blended cements in relation to various replacement ratios (0—50%). The waste brick consisted of SiO2 (63.21%), Al2O3 (16.41%), Fe2O3 (6.05%), Na2O (1.19%), K2O (2.83%) and MgO (1.11%), and had a pozzolanic activity index of 107%. The toxic characteristic leaching procedure (TCLP) results demonstrate that the heavy-metal content in waste bricks met the Environmental Protection Agency regulatory limits. Experimental results indicate that 10, 20, 30, 40 and 50% of cement can be replaced by waste brick, which causes the initial and final setting times to increase. Compressive strength development was slower in waste brick-blended cement (WBBC) pastes in the early ages; however, strength at the later ages increased significantly. Species analyses demonstrate that the hydrates in WBBC pastes primarily consisted of Ca(OH)2 and calcium silicate hydrate (C—S—H) gel, like those found in ordinary Portland cement (OPC) paste. Pozzolanic reaction products formed in the WBBC pastes, in particular, various reaction products, including hydrates of calcium silicates (CSH), aluminates (CAH) and aluminosilicates (CASH), formed as expected, resulting in consumption of Ca(OH)2 during the late ages of curing. The changes in the properties of WBBC pastes were significant as blend ratio increased, due to the pores of C—S—H gels and CAH filling via pozzolanic reactions. This filling of gel pores resulted in densification and subsequently enhanced the gel/space ratio and degree of hydration. Experimental results demonstrate waste brick can be supplementary cementitious material.

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Wen-Ming Chen

National Kaohsiung Marine University

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I-Son Ng

National Cheng Kung University

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Bin Xu

Southeast University

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Po-Wei Tsai

Chang Jung Christian University

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En-Hua Zhang

Chinese Academy of Sciences

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