Spelling suggestions: "subject:"microconstituents"" "subject:"microconstituent""
1 |
Sorption of Microconstituents onto Primary and Activated Sludge to which Alum Has Been AddedZhu, Ying January 2014 (has links)
Microconstituents (MCs) have become an emerging concern to scientists and researchers. Due to the development of analytical technology, it is now possible to study MCs at ηg/L to μg/L levels.
Wastewater treatment plants (WWTPs) are the major point source for MCs entering the environment based on the literature. WWTPs are known to be unable to remove many MCs to a safe level. In order to fully understand the fate of MCs in WWTPs and to further improve the design of WWTPs in terms of MC removal, it is necessary to examine removal mechanisms such as sorption and biodegradation in WWTPs.
Three MCs, bisphenol A (BPA), 17-α-ethinylestradiol (EE2) and triclosan (TCS), were chosen for this study. They are chemicals reported to be hydrophobic and have low vapor pressure, which makes sorption a highly potential removal mechanism.
Primary sludge and activated sludge (AS) were used to perform sorption kinetics and isotherm experiments for BPA, EE2 and TCS. Primary sludge was collected from local WWTPs, and AS was generated from a lab-scale continuous flow bioreactor system maintained at solids retention times of 15, 10 and 5 d and hydraulic retention time (HRT) of 6 h. Alum was added to synthetic wastewater influent at concentrations typically used for phosphorus removal at some plants. Alum has the potential to change sludge structure and influence the sorption process. A comparison was made with AS as the adsorbent with and without alum addition to the AS to study the influence of alum on the sorption processes.
The selected MCs were found to reach sorption equilibrium with primary sludge within 7 h. A pseudo second-order kinetic model was an excellent fit to describe the sorption processes of selected MCs.
The solids-liquid partitioning coefficient (Kd) was determined for the three chosen MCs. The Kd values found for primary sludge and AS are very close. The Kd for MCs sorbed to AS in this study were compared with the Kd for AS without alum addition. Although alum addition showed no influence on effluent soluble chemical oxygen demand, it decreases the Kd for BPA and EE2 sorbed to AS. In contrast, a much higher Kd for TCS was observed for AS with alum addition.
Judging from the R2 values, the linear sorption model is not suitable for some of the isotherms. Langmuir and Freundlich sorption isotherms were further used to fit the experimental data by applying linear regression and nonlinear regression approaches. The Freundlich isotherm was found to be the most suitable model to describe the experiment data.
|
2 |
General Fate Model for Microconstituents in an Activated Sludge SystemBanihashemi, Bahman January 2014 (has links)
Mathematical models elaborated for removal of microconstituents (MCs) in activated sludge (AS) system have not incorporated developments in International Water Association (IWA) models. In this thesis, sorption and biodegradation kinetic models that can be applied to describe transformation of MCs in an AS process were evaluated (volatilization and photodegradation were considered negligible).
Bisphenol-A (BPA), 17α-ethinylestradiol (EE2), and triclosan (TCS) have been selected as target compounds in this thesis. Sorption batch tests were conducted to retrieve kinetic and equilibrium data. Nine lab-scale continuous flow porous-pot bioreactors operating at various solids retention times (SRTs) and hydraulic retention times (HRTs) were studied for biodegradation of MCs. The effects of SRT, HRT and the biomass concentration on sorption and removal of MCs were also investigated and the results of each phase were incorporated into MCs fate models. Freundlich and linear sorption isotherms and pseudo-second-order kinetic models with different kinetic rates were found to best fit the sorption and desorption results. The result of biodegradation study in the presence of 20 µg/L of MCs demonstrated 90-98, 63-91 and 97-98% mean removal rates of BPA, EE2 and TCS, respectively, in systems operating at SRT of 5–15 d and HRT of 4-10 h. Calculation of mass fluxes of selected MCs in the dissolved and particulate phases showed that biotransformation was the principal removal mechanism of targeted MCs.
The fate models for the degradation mechanism of selected MCs were evaluated by applying various mathematical models. The pseudo-second-order model was found to best fit the results when active MCs degraders (XC) were used in the model. It was found that biodegradation studies should incorporate XC and not mixed liquor suspended solids concentration in their kinetic formulations. Therefore, the result of this study could be seen in the context, where the active MCs degraders are proposed to reduce the variability of biodegradation kinetic rates in AS systems operating at different operational conditions. Finally nitrification inhibitors, allylthiourea (ATU) were added to reactors and it was found that although nitrification process affects the fate of MCs in AS system, heterotrophs were most likely responsible for the biotransformation of the targeted MCs.
|
3 |
Evaluation of Biosolids as a Soil Amendment for Use in Ecological RestorationBusalacchi, Dawn M. 20 June 2012 (has links)
No description available.
|
Page generated in 0.0657 seconds