Abstract In-situ chlorine generation has high disinfection potential for small to medium scale wa... more Abstract In-situ chlorine generation has high disinfection potential for small to medium scale water treatment systems. Electrodes were prepared by coating Pt-, Ni-, Co-oxides on graphite substrate using electrodeless deposition method and characterized with SEM, EDS, XRD, XPS and cyclic voltammetry. Results showed that the molar ratio of Ni- and Co-oxides on graphite surface influenced surface structure and in-situ chlorine generation capacity. Pt0.01Ni0.24Co0.75 electrode exhibited a unique surface structure and the highest in-situ chlorine generation capability. The Pt0.01Ni0.24Co0.75-G electrode exhibited highly porous 3D structure and high oxygen deficit, which significantly promoted the formation of M-Cl- binding on electrode surface and enhanced chlorine generation. The onset of chlorine evolution potential was lower than that of oxygen on Pt0.01Ni0.24Co0.75-G electrode. Moreover, the transfer coefficient of chloride oxidation was smaller than that of water oxidation, which would enhance chloride oxidation current efficiency. The in-situ chlorine generation capability increased with NaCl concentration. The kinetics of chlorine generation was well described by the Langmuir-Hinsheldwood mechanism. The in-situ disinfection rate decreased with the increase in initial E. coli density. A 7.5-log disinfection was achieved in 15 min in the presence of 0.01 M NaCl under 5 mA/cm2 current density at room temperature. The lipid peroxide, morphology changes and destruction of E. coli cell membrane were observed in the in-situ disinfection process, indicating that reactive species such as chlorine radical in addition to free chlorine played the main role of in-situ disinfection.
Abstract The capability of manganese dioxide (MnO2) supported on loofah-derived activated carbon ... more Abstract The capability of manganese dioxide (MnO2) supported on loofah-derived activated carbon (AC) in the electrosorptive removal of common inert ions was studied in constant potential mode. Four MnO2 polymorphs were prepared by redox chemical precipitation and characterized by XRD, SEM, BET and XPS. The pseudocapacitance property of the MnO2/AC electrode, significantly affected by the surface- and diffusion-controlled charge storage mechanism, was assessed via voltammetry and modified Langmuir adsorption isotherm. Batch electrosorption experiments were then performed at constant potential in the range of −1.5 V to + 1.5 V (vs. Ag/AgCl) using AC and α-MnO2/AC electrodes in the presence of common simple electrolytes, including NaNO3, Li2SO4, and Ca(ClO4)2. Consequently, the applied working potential (Eapp) positively affected the ion electrosorption rate and capacity. Faradaic processes occurred on MnO2, i.e., Mn(III)/Mn(IV) transition, increased the diffusion capacitance of AC, thus enhancing the first-order rate and monolayer capacity, mainly for the electrosorption of cations. Results showed that ion solvation, controlled by the ionic radius and valence of an ion, which impacted ion intercalation in MnO2 and affected ion adsorption characteristics. The cation sorption capacity of α-MnO2/AC followed the order of Na+ (2.8 × 10-4 mol g−1) > Ca2+ (2.1 × 10-4 mol g−1) > Li+ (0.76 × 10-4 mol g−1) at Eapp = -1.5 V. The differential capacitance as affected by polarized potential and the shift of zero net charge or IEP toward more positively charging potential further highlighted the contribution of pseudocapacitance to ion adsorption on α-MnO2/AC electrode.
Dyes are hazardous compounds commonly found in industrial wastewaters. Efficient and inexpensive ... more Dyes are hazardous compounds commonly found in industrial wastewaters. Efficient and inexpensive removal of dye molecules from the water matrix has been demonstrated by adsorption processes. Magnetic nano-adsorbents, such as metal ferrites, can be efficiently recovered from the reaction mixture after treating the pollutant. Herein, MFe2O4@GO (M = Cu, Co or Ni) was synthesized via solution combustion method for the removal of dye molecules from aqueous solutions. The characteristics of the MFe2O4@GO, including surface area and pore diameter, surface functional groups, and elemental composition, were examined. Methylene blue was used as representative dye pollutant. Batch adsorption results conformed to the Langmuir isotherm. Maximum adsorption capacities of the MFe2O4@GO (M = Cu, Co or Ni) were 25.81, 50.15 and 76.34 mg g-1, respectively. Kinetics of methylene blue adsorption fitted the pseudo-second-order model. Overall, NiFe2O4@GO exhibited the highest adsorbent performance among the graphene-metal ferrites investigated, primarily because of its high specific surface area and presence of mesopores.
Various surfactants, such as nonionic Triton X-100 and Simple Green™ (SG), and anionic sodium dod... more Various surfactants, such as nonionic Triton X-100 and Simple Green™ (SG), and anionic sodium dodecylsulfate (SDS) and sodium dodecylbenzene sulfonate (SDBS) were utilized to remove polycyclic aromatic hydrocarbons (PAHs) from heavily contaminated harbor sediments dredged from Kaohsiung Harbor in Taiwan. Desorption/re-sorption equilibrium, kinetics, and washability of PAHs using the selected surfactant were evaluated under different critical micelle concentrations (CMC). Experimental results revealed that the desorption rate of high molecular weight PAHs was greater than those of low molecular weight PAHs, and the anionic SDS was relatively effective in the removal of total PAHs (>50%) compared to the other surfactants. The correlation between the effectiveness of the surfactant washing processes and the physicochemical properties of individual PAH was statistically analyzed. The resulting data suggested that hydrophobic factors (Kow, Koc and Sw) affected PAH treatability more than the reactivity of PAH (electron affinity and ionization potential). Since the adsorption of anionic surfactant altered the hydrophobicity of organic matter in the sediment, PAHs preferred transferring from the sediment to the hydrophobic core of micelles in aqueous solution. Nevertheless, the nonionic surfactant enhanced the PAH partition in the aqueous phase, thus increasing the micellar solubilization of PAH.
This work demonstrates the synthesis of a novel KMnO(4)-modified form of iron oxide, MnBT-4, usin... more This work demonstrates the synthesis of a novel KMnO(4)-modified form of iron oxide, MnBT-4, using a fluidized bed reactor (FBR) for the adsorptive removal of arsenic (III)/(V). Characterization by XRD, BET, and SEM indicated that the BT-4 support was poorly crystallized goethite (α-FeOOH) with a specific surface area of 229 m(2) g(-1). In FBR experiments of synthesizing MnBT-4, the Fe and Mn salts were found to have an optimal dosage ratio of less than 4, which maximized the KMnO(4) immobilization efficiency. The immobilized Mn compounds on MnBT-4 underwent an additional oxidation step of As (III), promoting arsenic adsorption. When applied MnBT-4 for As (III) removal from solution, the sorption isotherm was accurately fitted with Langmuir and Freundlich models, while the maximum adsorption capacity of 27.4 mg g(-1) exceeded those of other adsorbents in the literature. Batch experimental results revealed that both raw BT-4 and MnBT-4 could take up a large amount of As (V). However, the MnBT-4 provided a substantially higher As (III) removal efficiency than BT-4.
Abstract Mesoporous zirconium pyrophosphate(ZPP) adsorbents were synthesized, with six quaternary... more Abstract Mesoporous zirconium pyrophosphate(ZPP) adsorbents were synthesized, with six quaternary ammonium salts (Quats), namely, Octyltrimethylammonium (OTMA, C8), Decyltrimethylammonium (DCTMA, C10), Dodecyltrimethylammonium (DDTMA, C12), Tetradecyltrimethylammonium (TDTMA, C14), Hexadecyltrimethylammoium (HDTMA, C16), and Octadecyltrimethylammonium (ODTMA, C18), as template for studying fluoride adsorption. Quats of long carbon chain length significantly affected the specific surface area of mesoporous ZPP adsorbents. C18-ZPP exhibited the largest specific surface area and fluoride adsorption density. Fluoride adsorption density remained constant at pH 10–11. Langmuir adsorption isotherm described fluoride adsorption characteristics well. Results showed that mesoporous ZPP synthesized with C18 at Zr to C18 molar ratio of 0.57:1 exhibited the best fluoride adsorption capacity (32 mmol/g) among all ZPP adsorbents prepared at various Zr to C18 molar ratios. C18-ZPP exhibited two-fold increase in fluoride removal capacity compared to plain ZPP. The reusability of C18-ZPP was assessed by running fluoride removal at least five cycles. Mesoporous ZPP is a promising adsorbent for fluoride removal from water with much enhanced adsorption capacity, regenerability, and reusability.
Municipal and industrial wastewater can be a potential source of magnesium. Therefore, the develo... more Municipal and industrial wastewater can be a potential source of magnesium. Therefore, the development of magnesium recovery technology can both release the burden of wastewater treatment and help ...
Abstract In-situ chlorine generation has high disinfection potential for small to medium scale wa... more Abstract In-situ chlorine generation has high disinfection potential for small to medium scale water treatment systems. Electrodes were prepared by coating Pt-, Ni-, Co-oxides on graphite substrate using electrodeless deposition method and characterized with SEM, EDS, XRD, XPS and cyclic voltammetry. Results showed that the molar ratio of Ni- and Co-oxides on graphite surface influenced surface structure and in-situ chlorine generation capacity. Pt0.01Ni0.24Co0.75 electrode exhibited a unique surface structure and the highest in-situ chlorine generation capability. The Pt0.01Ni0.24Co0.75-G electrode exhibited highly porous 3D structure and high oxygen deficit, which significantly promoted the formation of M-Cl- binding on electrode surface and enhanced chlorine generation. The onset of chlorine evolution potential was lower than that of oxygen on Pt0.01Ni0.24Co0.75-G electrode. Moreover, the transfer coefficient of chloride oxidation was smaller than that of water oxidation, which would enhance chloride oxidation current efficiency. The in-situ chlorine generation capability increased with NaCl concentration. The kinetics of chlorine generation was well described by the Langmuir-Hinsheldwood mechanism. The in-situ disinfection rate decreased with the increase in initial E. coli density. A 7.5-log disinfection was achieved in 15 min in the presence of 0.01 M NaCl under 5 mA/cm2 current density at room temperature. The lipid peroxide, morphology changes and destruction of E. coli cell membrane were observed in the in-situ disinfection process, indicating that reactive species such as chlorine radical in addition to free chlorine played the main role of in-situ disinfection.
Abstract The capability of manganese dioxide (MnO2) supported on loofah-derived activated carbon ... more Abstract The capability of manganese dioxide (MnO2) supported on loofah-derived activated carbon (AC) in the electrosorptive removal of common inert ions was studied in constant potential mode. Four MnO2 polymorphs were prepared by redox chemical precipitation and characterized by XRD, SEM, BET and XPS. The pseudocapacitance property of the MnO2/AC electrode, significantly affected by the surface- and diffusion-controlled charge storage mechanism, was assessed via voltammetry and modified Langmuir adsorption isotherm. Batch electrosorption experiments were then performed at constant potential in the range of −1.5 V to + 1.5 V (vs. Ag/AgCl) using AC and α-MnO2/AC electrodes in the presence of common simple electrolytes, including NaNO3, Li2SO4, and Ca(ClO4)2. Consequently, the applied working potential (Eapp) positively affected the ion electrosorption rate and capacity. Faradaic processes occurred on MnO2, i.e., Mn(III)/Mn(IV) transition, increased the diffusion capacitance of AC, thus enhancing the first-order rate and monolayer capacity, mainly for the electrosorption of cations. Results showed that ion solvation, controlled by the ionic radius and valence of an ion, which impacted ion intercalation in MnO2 and affected ion adsorption characteristics. The cation sorption capacity of α-MnO2/AC followed the order of Na+ (2.8 × 10-4 mol g−1) > Ca2+ (2.1 × 10-4 mol g−1) > Li+ (0.76 × 10-4 mol g−1) at Eapp = -1.5 V. The differential capacitance as affected by polarized potential and the shift of zero net charge or IEP toward more positively charging potential further highlighted the contribution of pseudocapacitance to ion adsorption on α-MnO2/AC electrode.
Dyes are hazardous compounds commonly found in industrial wastewaters. Efficient and inexpensive ... more Dyes are hazardous compounds commonly found in industrial wastewaters. Efficient and inexpensive removal of dye molecules from the water matrix has been demonstrated by adsorption processes. Magnetic nano-adsorbents, such as metal ferrites, can be efficiently recovered from the reaction mixture after treating the pollutant. Herein, MFe2O4@GO (M = Cu, Co or Ni) was synthesized via solution combustion method for the removal of dye molecules from aqueous solutions. The characteristics of the MFe2O4@GO, including surface area and pore diameter, surface functional groups, and elemental composition, were examined. Methylene blue was used as representative dye pollutant. Batch adsorption results conformed to the Langmuir isotherm. Maximum adsorption capacities of the MFe2O4@GO (M = Cu, Co or Ni) were 25.81, 50.15 and 76.34 mg g-1, respectively. Kinetics of methylene blue adsorption fitted the pseudo-second-order model. Overall, NiFe2O4@GO exhibited the highest adsorbent performance among the graphene-metal ferrites investigated, primarily because of its high specific surface area and presence of mesopores.
Various surfactants, such as nonionic Triton X-100 and Simple Green™ (SG), and anionic sodium dod... more Various surfactants, such as nonionic Triton X-100 and Simple Green™ (SG), and anionic sodium dodecylsulfate (SDS) and sodium dodecylbenzene sulfonate (SDBS) were utilized to remove polycyclic aromatic hydrocarbons (PAHs) from heavily contaminated harbor sediments dredged from Kaohsiung Harbor in Taiwan. Desorption/re-sorption equilibrium, kinetics, and washability of PAHs using the selected surfactant were evaluated under different critical micelle concentrations (CMC). Experimental results revealed that the desorption rate of high molecular weight PAHs was greater than those of low molecular weight PAHs, and the anionic SDS was relatively effective in the removal of total PAHs (>50%) compared to the other surfactants. The correlation between the effectiveness of the surfactant washing processes and the physicochemical properties of individual PAH was statistically analyzed. The resulting data suggested that hydrophobic factors (Kow, Koc and Sw) affected PAH treatability more than the reactivity of PAH (electron affinity and ionization potential). Since the adsorption of anionic surfactant altered the hydrophobicity of organic matter in the sediment, PAHs preferred transferring from the sediment to the hydrophobic core of micelles in aqueous solution. Nevertheless, the nonionic surfactant enhanced the PAH partition in the aqueous phase, thus increasing the micellar solubilization of PAH.
This work demonstrates the synthesis of a novel KMnO(4)-modified form of iron oxide, MnBT-4, usin... more This work demonstrates the synthesis of a novel KMnO(4)-modified form of iron oxide, MnBT-4, using a fluidized bed reactor (FBR) for the adsorptive removal of arsenic (III)/(V). Characterization by XRD, BET, and SEM indicated that the BT-4 support was poorly crystallized goethite (α-FeOOH) with a specific surface area of 229 m(2) g(-1). In FBR experiments of synthesizing MnBT-4, the Fe and Mn salts were found to have an optimal dosage ratio of less than 4, which maximized the KMnO(4) immobilization efficiency. The immobilized Mn compounds on MnBT-4 underwent an additional oxidation step of As (III), promoting arsenic adsorption. When applied MnBT-4 for As (III) removal from solution, the sorption isotherm was accurately fitted with Langmuir and Freundlich models, while the maximum adsorption capacity of 27.4 mg g(-1) exceeded those of other adsorbents in the literature. Batch experimental results revealed that both raw BT-4 and MnBT-4 could take up a large amount of As (V). However, the MnBT-4 provided a substantially higher As (III) removal efficiency than BT-4.
Abstract Mesoporous zirconium pyrophosphate(ZPP) adsorbents were synthesized, with six quaternary... more Abstract Mesoporous zirconium pyrophosphate(ZPP) adsorbents were synthesized, with six quaternary ammonium salts (Quats), namely, Octyltrimethylammonium (OTMA, C8), Decyltrimethylammonium (DCTMA, C10), Dodecyltrimethylammonium (DDTMA, C12), Tetradecyltrimethylammonium (TDTMA, C14), Hexadecyltrimethylammoium (HDTMA, C16), and Octadecyltrimethylammonium (ODTMA, C18), as template for studying fluoride adsorption. Quats of long carbon chain length significantly affected the specific surface area of mesoporous ZPP adsorbents. C18-ZPP exhibited the largest specific surface area and fluoride adsorption density. Fluoride adsorption density remained constant at pH 10–11. Langmuir adsorption isotherm described fluoride adsorption characteristics well. Results showed that mesoporous ZPP synthesized with C18 at Zr to C18 molar ratio of 0.57:1 exhibited the best fluoride adsorption capacity (32 mmol/g) among all ZPP adsorbents prepared at various Zr to C18 molar ratios. C18-ZPP exhibited two-fold increase in fluoride removal capacity compared to plain ZPP. The reusability of C18-ZPP was assessed by running fluoride removal at least five cycles. Mesoporous ZPP is a promising adsorbent for fluoride removal from water with much enhanced adsorption capacity, regenerability, and reusability.
Municipal and industrial wastewater can be a potential source of magnesium. Therefore, the develo... more Municipal and industrial wastewater can be a potential source of magnesium. Therefore, the development of magnesium recovery technology can both release the burden of wastewater treatment and help ...
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