Title page for etd-0224112-154839


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URN etd-0224112-154839
Author Tsung-Hsiang Chou
Author's Email Address No Public.
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Department Environmental Engineering
Year 2011
Semester 2
Degree Master
Type of Document
Language zh-TW.Big5 Chinese
Title Removal of Environmental Hormones and Pharmaceuticals from Aqueous Solution via Nano-Fe3O4/S2O82- Oxidation Assisted by the Simultaneous Electrocoagulation/Electrofiltration Process
Date of Defense 2012-02-13
Page Count 216
Keyword
  • Tubular composite membrane
  • Electrocoagulation
  • Nano-Fe3O4
  • Pharmaceuticals
  • Environmental hormones
  • Sodium persulfate
  • Electrofiltration
  • Abstract Water recycling has become a global trend because of water scarcity and increased demand of water supply. Therefore, attentions to the improvement of reclaimed water quality have been paid. In the past decade various environmental hormones and PPCPs (pharmaceuticals and personal care products) have been detected in different aquatic environments. Even though their concentrations are in the range of ng/L to μg/L, these emerging contaminants might cause harm to human health and the environment. Nanoscale contaminants are another type of emerging contaminants cannot be neglected because many nanomaterials have been used in household goods of our daily lives. Thus, how to effectively separate and/or recover those nanomaterials from aqueous solution to reduce their potential hazards is an important issue
    The first objective of this study was to assess the efficiency of nano-Fe3O4/S2O82- oxidation against selected environmental hormones (i.e., di(2-ethylhexyl)phthalate (DEHP) and perfluorooctane sulphonates (PFOS)) and pharmaceuticals (i.e., erythromycin (ERY) and sulfamethoxazole (SMX)) in aqueous solution. The optimal operating conditions obtained from the above-indicated oxidation process were then transferred to a simultaneous electrocoagulation and electrofiltration (EC/EF) treatment module into which a tubular TiO2/Al2O3 composite membrane was incorporated. The purpose of this practice was to evaluate whether the EC/EF process could further enhance the removal of target contaminants.
    In this work nanoscale magnetite (nano-Fe3O4) used for activation of S2O82- oxidation was prepared by chemical coprecipitation. Then, X-ray powder diffractometry was used to confirm the crystal structure of the prepared particles as magnetite. The employment of 3 wt% soluble starch was found to be sufficient to stabilize nano-Fe3O4 for later uses. Further, slurries of nano-Fe3O4 and S2O82- (sodium persulfate) were prepared with three dosage ratios, namely 1:2.5, 1:5 and 1:10.
    Nano-Fe3O4/S2O82- slurries thus prepared were used for evaluating their efficiencies in removing target contaminants (i.e., DEHP, PFOS, ERY, and SMX) of two concentration levels. In this study the high concentration level referred to 38 mg/L for DEHP and 10 mg/L each for the rest of target contaminants, whereas 10 μg/L as the low concentration level for each of target contaminants. Batch experiments of nano-Fe3O4/S2O82- oxidation against target contaminants were first carried out in glass beakers. In the case of high concentration level with a nano-Fe3O4-to-S2O82- dosage ratio of 1:10, the respective removal efficiencies for all target contaminants were greater than 98%. Using the same dosage ratio for the case of low concentration level, however, the respective removal efficiencies for all target contaminants decreased to 78-91% except for ERY. When all target contaminants of low concentration level co-existed in the reaction vessel, the residual concentrations of environmental hormones were found to be greater than that of pharmaceuticals. Under the circumstances, the removal efficiency of DEHP dropped to 70% or so.
    The reaction pathways of nano-Fe3O4/S2O82- oxidation against each of target contaminants with a high concentration level were also investigated. The degradation intermediates detected for all target contaminants were all in line with the literature. Besides, the degradation intermediates were all close to their respective end products except those originated from DEHP. In other words, nano-Fe3O4/S2O82- per se had a phenomenal oxidation rate against each target contaminant.
    The performance of EC/EF-assisted nano-Fe3O4/S2O82- oxidation against target contaminants of low concentration level was also evaluated in this study. In each test every contaminated aqueous solution was physically preconditioned within the EC/EF treatment module for 20 min prior to the application of an electric field to enact electrocoagulation and electrofiltration. The optimal operating conditions obtained were given as follows: aluminum anode, electric field strength of 60 V/cm, transmembrane pressure of 98 kPa, and crossflow velocity of 3.33 cm/s. Under such conditions, the removal efficiencies for DEHP, PFOS, ERY, and SMX were determined to be 95%, 99%, 100%, and 99%, respectively. In the case of mixed environmental hormones and pharmaceuticals, the respective removal efficiencies slightly decreased to 85-99%. It is evident that the coupling of the EC/EF process with nano-Fe3O4/S2O82- oxidation yielded a substantial removal increase for selected target contaminants. Additionally, in all tests of EC/EF-assisted nano-Fe3O4/S2O82- oxidation against target contaminants, no residual nano-Fe3O4 was found in permeate. After a simple adjustment of pH, permeate thus treated would be ready for reuse in cooling towers.
    Advisory Committee
  • Daming Wang - chair
  • Shuchen Hsieh - co-chair
  • Gordon C. C. Yang - advisor
  • Files
  • etd-0224112-154839.pdf
  • Indicate in-campus at 5 year and off-campus access at 5 year.
    Date of Submission 2012-02-24

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