This study aimed to explore a new degradation method-photocatalysis technology to polish membrane bioreactor(MBR) effluent, using 2,6-di-tert-butylphenol(2,6-DTBP) as a model soluble microbial product(SMP).2,6-DTBP is...This study aimed to explore a new degradation method-photocatalysis technology to polish membrane bioreactor(MBR) effluent, using 2,6-di-tert-butylphenol(2,6-DTBP) as a model soluble microbial product(SMP).2,6-DTBP is one of the predominant SMPs in MBR effluent, which is refractory and difficult to biodegrade.This study developed a novel carboxylated graphene oxide/titanium dioxide/silver(GO-COOH/TiO2/Ag) nanocomposite to photodegrade 2,6-DTBP.GO-COOH/TiO2/Ag was successfully synthesized, using L-cysteine as the linker bonding TiO2/Ag to GO-COOH.The structural, morphological and optical properties of the GO-COOH/TiO2/Ag nanocomposite were characterized using various techniques.Owing to synergistic effects, the GO-COOH/TiO2/Ag nanocomposite exhibited enhanced photocatalytic degradation performance under solar light irradiation when compared to TiO2, Ag and GO-COOH.To remove 25 mg/L 2,6-DTBP, the reaction time for GOCOOH/TiO2/Ag was only 30 min, faster than the 90 min required for pure TiO2 or Ag.In addition, the 200 mg/L GO-COOH/TiO2/Ag nanocomposite aqueous solution showed the best performance under solar light, with 99% removal of 2,6-DTBP.This enhanced capability is likely due to the surface plasmon resonance(SPR) effect contributed by Ag nanoparticles(NPs) doped onto the TiO2.In addition, GO-COOH had a high effective surface area, which assisted in degrading the 2,6-DTBP through improved adsorption.The stability study showed that the photocatalytic activity of the GO-COOH/TiO2/Ag was stable enough for recycling multiple times.The effective degradation performance and excellent stability demonstrates that the GO-COOH/TiO2/Ag nanocomposite can be a promising photocatalyst in the field of effluent SMP photodegradation, which solves the problem of the difficult biodegradation of highly toxic 2,6-DTBP.展开更多
Scanning Mobility Particle Sizer (SMPS) spectrometers are subject to several restrictions when a radioactive source is employed to bring the aerosol to a steady-state charge distribution. An alternative solution, comm...Scanning Mobility Particle Sizer (SMPS) spectrometers are subject to several restrictions when a radioactive source is employed to bring the aerosol to a steady-state charge distribution. An alternative solution, commercially available, is represented by the soft X-ray neutralizer. The present study investigates the outcome of a combination of a Grimm SMPS, which employs a 241Am radioactive source, with the soft X-ray advanced aerosol neutralizer (TSI model 3087). To date, the latter device has been interfaced only with TSI’s Electrostatic Classifiers. Particle size distribution of sodium chloride aerosol was measured with both neutralizers and it was found that the particle number concentration agreed to be within 9% for the 10 - 700 nm range. This difference mainly corresponds to the bias reported by TSI, when the X-ray device is mounted on a TSI spectrometer. It was concluded that the X-ray neutralizer could be usefully employed, as a standalone device, in combination with Grimm Electrostatic Classifiers.展开更多
基金the financial support received from China Postdoctoral Science Foundation Funded Project(No.2018M641387).
文摘This study aimed to explore a new degradation method-photocatalysis technology to polish membrane bioreactor(MBR) effluent, using 2,6-di-tert-butylphenol(2,6-DTBP) as a model soluble microbial product(SMP).2,6-DTBP is one of the predominant SMPs in MBR effluent, which is refractory and difficult to biodegrade.This study developed a novel carboxylated graphene oxide/titanium dioxide/silver(GO-COOH/TiO2/Ag) nanocomposite to photodegrade 2,6-DTBP.GO-COOH/TiO2/Ag was successfully synthesized, using L-cysteine as the linker bonding TiO2/Ag to GO-COOH.The structural, morphological and optical properties of the GO-COOH/TiO2/Ag nanocomposite were characterized using various techniques.Owing to synergistic effects, the GO-COOH/TiO2/Ag nanocomposite exhibited enhanced photocatalytic degradation performance under solar light irradiation when compared to TiO2, Ag and GO-COOH.To remove 25 mg/L 2,6-DTBP, the reaction time for GOCOOH/TiO2/Ag was only 30 min, faster than the 90 min required for pure TiO2 or Ag.In addition, the 200 mg/L GO-COOH/TiO2/Ag nanocomposite aqueous solution showed the best performance under solar light, with 99% removal of 2,6-DTBP.This enhanced capability is likely due to the surface plasmon resonance(SPR) effect contributed by Ag nanoparticles(NPs) doped onto the TiO2.In addition, GO-COOH had a high effective surface area, which assisted in degrading the 2,6-DTBP through improved adsorption.The stability study showed that the photocatalytic activity of the GO-COOH/TiO2/Ag was stable enough for recycling multiple times.The effective degradation performance and excellent stability demonstrates that the GO-COOH/TiO2/Ag nanocomposite can be a promising photocatalyst in the field of effluent SMP photodegradation, which solves the problem of the difficult biodegradation of highly toxic 2,6-DTBP.
文摘Scanning Mobility Particle Sizer (SMPS) spectrometers are subject to several restrictions when a radioactive source is employed to bring the aerosol to a steady-state charge distribution. An alternative solution, commercially available, is represented by the soft X-ray neutralizer. The present study investigates the outcome of a combination of a Grimm SMPS, which employs a 241Am radioactive source, with the soft X-ray advanced aerosol neutralizer (TSI model 3087). To date, the latter device has been interfaced only with TSI’s Electrostatic Classifiers. Particle size distribution of sodium chloride aerosol was measured with both neutralizers and it was found that the particle number concentration agreed to be within 9% for the 10 - 700 nm range. This difference mainly corresponds to the bias reported by TSI, when the X-ray device is mounted on a TSI spectrometer. It was concluded that the X-ray neutralizer could be usefully employed, as a standalone device, in combination with Grimm Electrostatic Classifiers.
