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<title>Environmental &amp; Water Resources Engineering Masters Projects</title>
<copyright>Copyright (c) 2013 University of Massachusetts - Amherst All rights reserved.</copyright>
<link>http://scholarworks.umass.edu/cee_ewre</link>
<description>Recent documents in Environmental &amp; Water Resources Engineering Masters Projects</description>
<language>en-us</language>
<lastBuildDate>Fri, 25 Jan 2013 18:19:22 PST</lastBuildDate>
<ttl>3600</ttl>





<item>
<title>Two-Stage Filtration to Control Manganse and DBPS at the Lantern Hill Water Treatment Plant</title>
<link>http://scholarworks.umass.edu/cee_ewre/51</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/51</guid>
<pubDate>Wed, 08 Feb 2012 13:16:24 PST</pubDate>
<description>
	<![CDATA[
	<p>This research involved full- and pilot-scale studies of treatment of the Aquarion</p>
<p>Water Company (AWC) Lantern Hill groundwater source. With elevated levels of both</p>
<p>dissolved manganese (~0.19 mg/L), dissolved iron (~1.9 mg/L) and natural organic</p>
<p>matter (NOM) (~3 mg/L) the existing treatment plant is having difficulty in achieving</p>
<p>required manganese removal while maintaining low concentrations of disinfection byproducts</p>
<p>(DBPs) in finished water. At full-scale, dissolved manganese in the raw water is</p>
<p>removed through pre-filter oxidation and adsorption on iron precipitates via application</p>
<p>of free chlorine and permanganate as well as adsorption of dissolved manganese onto</p>
<p>MnO</p>
<p>x(s) coated filter media (anthracite and greensand) which is continuously reactivated</p>
<p>by free-chlorine oxidation. The addition of pre-filter chlorine to the raw water with high</p>
<p>concentration of NOM leads to the formation of elevated levels of regulated DBPs such</p>
<p>as trihalomethanes (THMs) and haloacetic acids (HAAs).</p>

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</description>

<author>Pham, Minh</author>

<source></source>

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<title>Utilizing a Decision Support System to Optimize Reservoir Operations to Restore the Natural Flow Distribution in the Connecticut River Watershed</title>
<link>http://scholarworks.umass.edu/cee_ewre/50</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/50</guid>
<pubDate>Wed, 08 Feb 2012 13:16:21 PST</pubDate>
<description>
	<![CDATA[
	<p>Reservoir development on the Connecticut River Basin has altered the natural hydrograph and detrimentally affected the region's aquatic ecosystems that thrive on natural variability.  This thesis examines ways in which flows in the river and its triburaries can be returned to a more natural regime withouy negatively impacting other users.  The analysis offers alternative operations to meet the various objectives as well as evaluates the impacts of climate change on the basin.  This paper focuses on the upper third of the basin as a proof of concept to demonstrate the decision support system and to generate initial results for the large effort.</p>

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</description>

<author>Pitta, Brian</author>

<source></source>

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<title>Advanced Oxidation of Drinking Water using Ultraviolet Light and Alternative Solid Forms of Hydrogen Peroxide</title>
<link>http://scholarworks.umass.edu/cee_ewre/49</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/49</guid>
<pubDate>Wed, 08 Feb 2012 11:49:37 PST</pubDate>
<description>
	<![CDATA[
	<p>With the increasing focus on removing emerging, unregulated drinking water contaminants, the use of advanced oxidation processes (AOPs) has become more prevalent. A commonly used AOP is the ultraviolet light/hydrogen peroxide (UV/H2O2) less harmful forms. In this analysis, two alternative solid forms of H AOP. This process utilizes the formation of hydroxyl radicals to oxidize contaminants to 2O2, sodium perborate (SPB) and sodium percarbonate (SPC) were used as sources of H 2O2 in the UV/H2O2 AOP. The potential advantage of SPB and SPC is that they are solids in nature,  and as a result, the shipping costs and shipping energy requirements can be reduced significantly compared to that of liquid H 2O2.</p>

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</description>

<author>Monge, Zachary F.</author>

<source></source>

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<title>Remote Sensing Models of Algal Blooms and Cyanobacteria in Lake Champlain</title>
<link>http://scholarworks.umass.edu/cee_ewre/48</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/48</guid>
<pubDate>Mon, 06 Feb 2012 09:44:58 PST</pubDate>
<description>
	<![CDATA[
	<p>We developed empirical remote sensing models to estimate chlorophyll</p>
<p><em>a </em>concentrations and</p>
<p>cyanobacteria synoptically, over a large inland lake using available Landsat Enhanced Thematic</p>
<p>Mapper Plus (ETM+) data. In contrast to previous studies which rely on the spectral</p>
<p>characteristics of the cyanobacterial specific pigment, phycocyanin, we developed remote</p>
<p>sensing models capable of directly detecting cyanobacterial biovolume. This distinction is</p>
<p>important because Landsat ETM+ data lacks the spectral band information required for optimal</p>
<p>phycocyanin detection. Each model was calibrated and cross-validated with existing</p>
<p><em>in situ</em></p>
<p><em> </em></p>
<p>measurements</p>
<p>from Lake Champlain’s Long-Term Water Quality and Biological Monitoring</p>
<p>Program (LTMP). Lake station measurements taken between 2006 and 2009 were matched with</p>
<p>radiometrically converted exoatmospheric reflectance data from seven spectral bands on the</p>
<p>Landsat ETM+ sensor. Step-wise multi-linear regression indicated data from Landsat ETM+</p>
<p>bands 1, 2 and 3 were most significant for predicting chl-</p>
<p><em>a </em>and cyanobacteria biovolume. Based</p>
<p>on statistical analysis, the linear models that included visible band ratios slightly outperformed</p>
<p>single band models. The final models captured the extents of cyanobacterial blooms throughout</p>
<p>the 2006-2009 study period. The results serve as an added monitoring tool for resource</p>
<p>managers and present new insight into the initiation and propagation of cyanobacterial blooms in</p>
<p>Lake Champlain.</p>

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</description>

<author>Trescott, Adam</author>

<source></source>

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<item>
<title>Biodegradation of Ethylene Dibromide (EDB)  Under In Situ and Biostimulated Conditions at  MMR</title>
<link>http://scholarworks.umass.edu/cee_ewre/47</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/47</guid>
<pubDate>Mon, 06 Feb 2012 09:43:02 PST</pubDate>
<description>
	<![CDATA[
	<p>An extensive microcosm study was conducted to investigate the biodegradation of 1,2-dibromoethane (EDB) under  <em>in situ </em>and biostimulated conditions within a plume at the Massachusetts Military Reservation in Cape Cod, MA. This particular EDB plume is unique because it has persisted for over 38 years, is more than 61 m below the ground surface, and has both aerobic and anaerobic zones with EDB levels above the maximum contaminant level (MCL) of 0.05 μg/L (ppb). Microcosms were constructed with <em>in situ </em>materials and conducted under environmentally relevant conditions (field EDB concentrations; incubated at 12°C). The results showed that natural attenuation occurred under anaerobic conditions but not under aerobic conditions. The lack of natural attenuation occurring in the aerobic zone, which is much larger than the anaerobic zone, offers valuable insight as to why EDB is so persistent at this site. EDB degradation rates were greater under biostimulated conditions for both the aerobic and anaerobic microcosms. On average, methane-amended aerobic microcosms degraded EDB at a first order rate eight times faster than unamended microcosms with the best performing replicate showing EDB degradation at a rate of 7.0 yr-1 (half-life (t1/2) = 0.10 yr). The lactate amended anaerobic microcosms degraded EDB at an average first order rate of 3.5 yr-1 (t1/2 = 0.20 yr) which was 19% faster than the unamended anaerobic microcosms. These results indicate potential for enhanced natural attenuation at the FS-12 site, especially under aerobic conditions.</p>

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</description>

<author>McKeever, Robert</author>

<source></source>

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<title>Conventional Water Treatment Processes for Removing Pharmaceutical and  Endocrine Disrupting Compounds</title>
<link>http://scholarworks.umass.edu/cee_ewre/46</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/46</guid>
<pubDate>Mon, 06 Feb 2012 09:41:02 PST</pubDate>
<description>
	<![CDATA[
	<p>Endocrine disrupting chemicals (EDCs) are natural or synthetic compounds that act like hormones in the endocrine system and disrupt the physiologic function of endogenous hormones. Although no standards concerning EDCs in drinking water have been established, there are rising concerns about the effects of EDCs in drinking water on human health.</p>
<p>The main objective of this study is to conduct bench scale experiments to investigate the effectiveness of conventional drinking water treatment processes at removing selected endocrine disrupting compounds (EDCs), pharmaceutical and personal care products (PPCPs) from municipal water supplies. It was also a goal of this work to provide utilities with information on likely removal of these compounds under a board range of water qualities and treatment scenarios.</p>
<p>Raw water used for this work came from 15 participating utilities, and each utility had at least one source water and treatment system. Samples were collected at different times of the year, and important water quality parameters, such as UV254, TOC and DOC were measured. The concentration of the target compounds in the raw water, travel blank, and treated water was also measured.</p>
<p>Overall, the treatment processes that include oxidation such as ozonation, chlorination and chloramination are the most effective processes resulting in around 80% to 100% of the target compounds removal. Chlorination alone is very effective at removing most of the target compounds that were studied. N-N-diethyltoluamide (DEET) and Tris (2 chloroethyl) phosphate (TCEP) are relatively resistant to all the treatment techniques that were tested (coagulation, ozonation, chlorination, chloramination and GAC/dual-media filtration).</p>
<p>However, filtration on adsorptive media was able to remove most of the DEET when the DEET concentration was low. This could be due to the result of adsorption on the GACmedia. The ozone-GAC biofiltration process is very effective at controlling and removing most target compounds.</p>

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</description>

<author>Lin, Jing</author>

<source></source>

</item>


<item>
<title>2-D Spill Modeling in the Wachusett Reservoir with CEQUAL-W2 for Years 2003-2006</title>
<link>http://scholarworks.umass.edu/cee_ewre/45</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/45</guid>
<pubDate>Mon, 06 Feb 2012 09:35:37 PST</pubDate>
<description>
	<![CDATA[
	<p>This study examines the effects of various environmental conditions on the behavior of a</p>
<p>contaminant spill as it travels across the Wachusett Reservoir. The reservoir, located in central</p>
<p>Massachusetts, is a 65 billion gallon water body that supplies drinking water to the Boston</p>
<p>Metropolitan area and consists of numerous inflows and outflows. The Quabbin Reservoir, a</p>
<p>412 billion gallon system, accounts for close to half of the inflow. The Wachusett Reservoir</p>
<p>receives Quabbin water through the Quabbin aqueduct located on its eastern side. CEQUAL</p>
<p>W2, a two-dimensional, laterally averaged, hydrodynamic and water quality model was utilized</p>
<p>to perform numerous simulations. The current version, version 3.6, was used due to its</p>
<p>computational speed and ability to apply past years data without changing input files.</p>
<p>Four years were analyzed, 2003-2006, in order to examine similarities and differences from year</p>
<p>to year. Simulations for years 2005 and 2006 were calibrated to measured temperature and</p>
<p>conductivity profiles within the North Basin of the Wachusett Reservoir (Years 2003 and 2004</p>
<p>were completed prior to this research). Simulations were performed in order to better understand</p>
<p>the behavior of the spill under three main scenarios: 1) seasonal change, 2) variation of spill</p>
<p>temperature, and 3) turning the Quabbin transfer on or off. Spill characteristics and location</p>
<p>were kept the same for each simulation to allow for comparison. The date of the spill was</p>
<p>chosen based on similar wind conditions for each season of every year. The behavior of the spill</p>
<p>was evaluated by analyzing conductivity versus time at the withdrawal of the reservoir, the</p>
<p>Cosgrove intake. Profiles of conductivity versus water depth at some locations along the</p>
<p>reservoir were observed in order to better understand spill behavior.</p>
<p>Model results demonstrated that similarities between years existed. The arrival time of the spill</p>
<p>was affected by the seasonal change. Spring spills consistently arrived at the withdrawal within</p>
<p>2-3 days, fall spills within approximately 7-10 days, and summer spills took 10-15 days. The</p>
<p>summer spills showed more variability, having larger peaks than the other seasons. Changing</p>
<p>the temperature of the spill displayed minimal effect for the spring and fall seasons. The summer</p>
<p>of 2004 showed a faster arrival time at the intake for a warm spill whereas the summers of 2003,</p>
<p>2005 and 2006 displayed negligible differences in spill behavior when changing the spill</p>
<p>temperature. Altering the condition of the Quabbin transfer showed the most effect during the</p>
<p>summer months for all four years. Turning the transfer off for a period of two weeks after the</p>
<p>significantly. CEQUAL W2 V3.6 proved to be an effective tool in examining the behavior of a</p>
<p>contaminant spill within the Wachusett Reservoir under various scenarios.  spill caused the variability of spill concentration measured at the withdrawal to dampen</p>

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</description>

<author>Sojkowski, Bryan R.</author>

<source></source>

</item>


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<title>Sub-Daily Multi-Objective Models for Optimizing Hydropower in the Deerfield River</title>
<link>http://scholarworks.umass.edu/cee_ewre/44</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/44</guid>
<pubDate>Mon, 30 Jan 2012 13:20:52 PST</pubDate>
<description>
	<![CDATA[
	
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</description>

<author>Adamec, Kelcy</author>

<source></source>

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<title>High-Strength Wastewater Treatment by Microalgae</title>
<link>http://scholarworks.umass.edu/cee_ewre/43</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/43</guid>
<pubDate>Mon, 30 Jan 2012 12:45:55 PST</pubDate>
<description>
	<![CDATA[
	<p>Microalgae spontaneously convert CO</p>
<p>2 and supplementary nutrients into biomass in the presence of light via photosynthesis, and at much higher rates than convention oil-producing crops. Algal biomass can then be transformed into methane via anaerobic bacteria-mediated fermentation, or to biodiesel via lipid extraction, as well as other by-products of secondary metabolism. Production of biofuel by microalgae can be made more sustainable through coupling microalgal biomass production with existing power generation and wastewater treatment infrastructure. On the other hand, integration of algal biofuel production into wastewater treatment plant anaerobic digestion infrastructure has the potential to increase biogas production, decrease high and variable internal nitrogen loads, and improve sludge digestibility and dewaterability</p>

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</description>

<author>Yuan, Xin</author>

<source></source>

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<title>Characterization of Proteins in Effluents from Three Wastewater Treatment Plants that Discharge to the Connecticut River</title>
<link>http://scholarworks.umass.edu/cee_ewre/42</link>
<guid isPermaLink="true">http://scholarworks.umass.edu/cee_ewre/42</guid>
<pubDate>Mon, 30 Jan 2012 12:17:08 PST</pubDate>
<description>
	<![CDATA[
	<p>This research characterizes the proteins in domestic wastewater treatment plant effluents in order to understand the organic fraction of effluent nitrogen. Domestic wastewater treatment plants have been identified as a major source of excess nitrogen that leads to eutrophication in marine environments in general, and the Long Island Sound, in particular. Initiatives to reduce the nitrogen load into Long Island Sound are underway. In Connecticut, regulators have instituted a cap and trade program for nitrogen releases from wastewater treatment plants, and in western Massachusetts new NPDES permits are requiring facilities that release into receiving waters that flow into the sound to monitor and report influent and effluent nitrogen concentrations. The total nitrogen released by wastewater treatment facilities can be successfully reduced through the addition of a nitrification/ denitrification process that removes inorganic nitrogen; however, the process does not remove most of the organic nitrogen. While proteins comprise a significant fraction of wastewater effluent organic carbon and nitrogen, they have not been extensively characterized, and little is known about their fate in the environment.</p>

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</description>

<author>Westgate, Pamela J.</author>

<source></source>

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