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<title>Senior Design Reports (CBE)</title>
<copyright>Copyright (c) 2013 University of Pennsylvania All rights reserved.</copyright>
<link>http://repository.upenn.edu/cbe_sdr</link>
<description>Recent documents in Senior Design Reports (CBE)</description>
<language>en-us</language>
<lastBuildDate>Wed, 23 Jan 2013 18:07:49 PST</lastBuildDate>
<ttl>3600</ttl>








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<title>Production of Acetaldehyde from Acetic Acid</title>
<link>http://repository.upenn.edu/cbe_sdr/45</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/45</guid>
<pubDate>Fri, 26 Oct 2012 13:07:40 PDT</pubDate>
<description>
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	<p>Our group has designed a process to manufacture 101,520,000 lb/yr of acetaldehyde by hydrogenation of acetic acid over a 20% wt. palladium on iron oxide catalyst. The reaction conditions used are the optimum according to a patent filed by Eastman Chemical (Tustin, et.al., U.S. Patent No. 6,121,498): temperature is range is from 557-599 °F at a pressure of 254 psi. The conversion of acetic acid in the reactor is 46 %, with selectivity of 86% to acetaldehyde. Major by-products are ethanol, acetone, carbon dioxide, and the light hydrocarbons methane, ethane, and ethylene. Acetaldehyde is purified in a series of steps: it is first absorbed with an acetic-acid rich solvent, then distilled to separate acetaldehyde from heavier components. A refrigerated condenser is then used to recover additional acetaldehyde from the vapor distillate of the main separation. Acetic acid is purified and recycled to the reactor to limit the amount of feedstock required.  Ethyl acetate is produced as a by-product in the acetaldehyde distillation column and is purified and sold.</p>
<p>The economics of the process is strongly dependent on the price of acetic acid, and we examined scenarios under which acetic acid was available at either $0.16/lb or $0.12/lb. The total capital investment in either situation is approximately $47,000,000. If acetic acid is available at $0. 16/1b, we estimate an IRR of 11.3 %, but if acetic acid can be purchased for $0.12/Ib the IRR is 18.5% after 20 years. It is our recommendation to pursue more research into projecting both the cost of acetic acid and the market for acetaldehyde. If acetic acid will be available at the lower price, the company should pursue production of acetaldehyde.</p>

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<author>Calvin daRosa et al.</author>


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<title>CELLULOSE TO COKE BOTTLES</title>
<link>http://repository.upenn.edu/cbe_sdr/44</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/44</guid>
<pubDate>Mon, 20 Aug 2012 11:37:02 PDT</pubDate>
<description>
	<![CDATA[
	<p>This project explores the plant-scale process design and economic viability of production of ethylene glycol using a patented direct route from cellulose. Switchgrass was selected as the source of cellulose because it is a low-cost, non-feedstock plant capable of growing under a variety of conditions. The plant is designed to produce 100 million pounds of 99.5 % pure ethylene glycol which is the required purity for ethylene glycol used in plastic bottle production. The project is environmentally friendly and meets the Federal and state emission regulations.</p>
<p>The process design consists of three major components: pre-treatment, reaction and separation. In the pre-treatment stage, the switchgrass is ground and cellulose is extracted using highly dilute base. The reaction occurs in water solvent under 5 MPa of hydrogen in a fixed bed catalytic reactor with a retention time of 30 minutes. The ethylene glycol product is separated from the solvent and byproducts by flash vessels and column distillation in order to attain 99.5 % purity. A side product, propylene glycol, is also produced at 99.5 % purity and is separated in a similar fashion.</p>
<p>For the economic analysis, the plant was assumed to be located in Tennessee (near the Gulf Coast) where switchgrass is readily available. The total capital investment is $349,000,000, including a working capital of $7,747,000. The process is sensitive to the amount of solvent used. In the base case scenario using the same amount of solvent as used in the patent with ethylene glycol priced at $0.50/lb, propylene glycol byproduct priced at $0.78/lb, switchgrass priced at $50/dry ton, hydrogen priced at $1.00/lb, and catalyst priced at $5.08/lb, the net present value (NPV) of the project is negative $565,500,000 based on an interest rate of 15%, and the investor’s rate of return (IRR) is negative. The process is not profitable under the current conditions but may become profitable with advances in technology as described by the sensitivity analysis section of the report. Although the current version of the process is unprofitable, it is expect that the further development of the technology described in the referenced patent will allow for profitable future versions of this process, and it is recommended by the design team that the management retain this report for future reference</p>

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<author>Quyen Dinh et al.</author>


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<title>COAL AND NATURAL GAS TO LIQUID ALKANES BY HYBRID PROCESSING</title>
<link>http://repository.upenn.edu/cbe_sdr/43</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/43</guid>
<pubDate>Mon, 20 Aug 2012 11:37:01 PDT</pubDate>
<description>
	<![CDATA[
	<p>This report describes a process to convert coal and natural gas to a mixture of liquid hydrocarbons, which is intended to be sold as a feedstock for a refinery. Given that the region has a large amount of coal production and sits atop the Marcellus shale with its expanding natural gas production, as well as the proximity to refineries in Ohio, southwestern Pennsylvania is a natural location for such a venture.</p>
<p>2600 tons per day of coal and 66 million standard cubic feet per day of natural gas are converted to syngas in separate, parallel process trains. The hydrogen rich natural gas syngas is mixed with the hydrogen lean coal syngas to give the desired syngas composition. Fischer-Tropsch chemistry is used to convert syngas with a 2 to 1 H<sub>2</sub>:CO molar ratio to a distribution of alkanes. The alkanes are separated to give 15,500 barrels per day of liquid product.</p>
<p>The total capital investment of the project was estimated to be $1,308 million. Using the EIA baseline projection for the price of oil and a 15% discount rate, the project is expected to have a net present value of -$258 million, with an internal rate of return of 11%. The profitability of the project is especially dependent on the price of oil and the total capital investment.</p>

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<author>Pat Driscoll et al.</author>


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<title>TWO-STEP PRODUCTION OF 1,3-BUTADIENE FROM ETHANOL</title>
<link>http://repository.upenn.edu/cbe_sdr/42</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/42</guid>
<pubDate>Mon, 20 Aug 2012 11:36:59 PDT</pubDate>
<description>
	<![CDATA[
	<p>A plant utilizing a two-step reaction process, which takes a 95% ethanol stream (by mass) and produces a 98% 1,3-butadiene stream, was designed for this project. The production goal for this plant was 200,000 tonnes of butadiene with the main motivation behind the project being the recent rise in butadiene prices. The process first passes ethanol through a catalytic dehydrogenation reactor to convert ethanol to acetaldehyde and hydrogen. A kinetic model was used to determine the reaction rates and operating conditions of the reactor. The acetaldehyde intermediate is further reacted with ethanol in a catalytic reactor to form butadiene. A hydrogen byproduct stream is also generated in this design and is purified for sale.</p>
<p>This report provides a design and economic analysis for the production of butadiene on the Gulf Coast. Process flow sheets, energy and utility requirements, and equipment summaries are provided and analyzed. Process profitability is sensitive to the cost of both ethanol and butadiene. It is shown that the plant is very profitable for its expected 15-year lifespan with an expected internal rate of return of 40%, return on investment of 34%, and net present value of $172,000,000 (for a discount rate of 15%). The process becomes unprofitable if the price of ethanol increases to over $3.00/gallon. A combination of increased ethanol price and decreased butadiene price will also cause the plant to be unprofitable. Therefore, plant construction is only recommended given an acceptable price of ethanol and butadiene.</p>

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<author>Jonathan Burla et al.</author>


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<title>DIRECT ROUTE TO PHENOL FROM BENZENE</title>
<link>http://repository.upenn.edu/cbe_sdr/41</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/41</guid>
<pubDate>Mon, 20 Aug 2012 11:36:57 PDT</pubDate>
<description>
	<![CDATA[
	<p>This report contains a preliminary process design for a direct route to phenol from benzene based on the 2009 patent issued to the Council of Scientific Research in New Delhi. This patent describes a significantly improved method to produce phenol using a vanadyl pyrophosphate catalyst. The process evades over-oxidized byproducts and yield loss. The resulting design produces the desired 500 million pounds per year of phenol by combining the ideas presented in the patent and adjustments made by the design group. The optimal process presented utilizes two parallel series of three reactors each to produce the phenol. Through a combination of azeotropic distillation and flash vaporization, it is possible to achieve greater than 99 percent pure phenol as a product while recycling all components not consumed. The plant requires a capital investment of 85.7 million USD with an internal rate of return of 4.98 percent and return on investment of 1.48 percent. It is suggested that the research and development department greatly improve the catalyst activity while maintaining the selectivity to phenol. Such improvements would enable the plant presented in this design to be economically feasible based on the current market for phenol.</p>

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<author>Alp Kutlu et al.</author>


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<title>Heat Recovery from Natural Gas Liquefaction Process</title>
<link>http://repository.upenn.edu/cbe_sdr/40</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/40</guid>
<pubDate>Mon, 20 Aug 2012 11:36:56 PDT</pubDate>
<description>
	<![CDATA[
	<p>This project recommends several possible processes which expand and improve upon an existing section of a natural gas liquefaction plant. The section in question involves the combustion of the effluent fuel from the liquefaction process to produce usable work that drives the overall process. The existing process involves a simple gas turbine, which utilizes a Brayton cycle to convert combustion heat to shaft work.</p>
<p>While the existing platform successfully provides power to the overall liquefaction process, the gaseous exhaust from this process leaves the system at elevated temperatures. The processes presented in this project seek to recover the heat that is lost through the exhaust and therefore, improve the thermodynamic efficiency of this system. Additionally, these processes more rigorously meet environmental standards concerning flue gas compositions and temperatures. Seven such processes are presented in this report. Each of these provides a net of 40MW, the required power to drive the liquefaction process, while performing at higher thermodynamic efficiencies than the simple gas turbine process.</p>
<p>Rigorous economic analyses were performed for each of the presented processes. One recovery system has a lower net present value (NPV) than that of the simple gas turbine, four have approximately equal NPVs, and two systems have significantly better NPVs than that of the simple gas turbine. The optimal system has an NPV of $22 million and an internal rate of return (IRR) of 28.2% versus the simple gas turbine with an NPV of $12.3 million and an IRR of 20.3%. Further analyses of the economic and pricing assumptions may be required before final project approval.</p>

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<author>Michelle Calabrese et al.</author>


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<title>Process Design for the Production of Ethylene from Ethanol</title>
<link>http://repository.upenn.edu/cbe_sdr/39</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/39</guid>
<pubDate>Mon, 20 Aug 2012 11:36:54 PDT</pubDate>
<description>
	<![CDATA[
	<p>This project considers using ethanol dehydration as a means to mass-produce ethylene. 2.3MM tonnes of a 95% ethanol / 5% water feed will be converted into 1MM tonnes of 99.96% pure ethylene per year using a series of adiabatic, fixed-bed catalytic reactors operating at 750°F and 600psi. The catalyst is gamma-alumina in the form of 1cm diameter spherical pellets. After the dehydration process, the product will be purified using two flash separation units, an adsorption unit with zeolite 13X sorbent, and finally a cryogenic distillation unit. The plant will be located in São Paulo, Brazil. Because ethanol production in Brazil is seasonal, the plant will operate only 280 days per year at a very high capacity. This includes 30 days worth of on-site feed storage. After conducting an analysis of the sensitivity of the plant’s Net Present Value and Internal Rate of Return to ethylene and ethanol prices, it was determined that while profitability is not attainable in the current market (which prices ethanol at $0.34/lb and ethylene at $0.60/lb), profitability is attainable should ethylene prices rise to $0.64/lb and ethanol prices fall to $0.305/lb.</p>

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<author>Gregory Cameron et al.</author>


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<title>Reclamation of Isopropyl Alcohol and N-Propyl Bromide</title>
<link>http://repository.upenn.edu/cbe_sdr/38</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/38</guid>
<pubDate>Mon, 20 Aug 2012 11:36:53 PDT</pubDate>
<description>
	<![CDATA[
	<p>The purpose of this design project is to recover a co-solvent mixture that is used to remove oil and water from metal machine parts. The cleansing solvents used are n-propylbromide (NPB) and isopropyl alcohol (IPA), which respectively remove oleic acid and water. The solvent mixture starts at an IPA/NPB molar ratio of 56/44 and can be used for cleaning machinery until the water reaches 7.5% by mole. This spent cleaning mixture is then delivered for reclamation of IPA and NPB so that it can be used for cleaning again. A 6,240 gallon truckload is delivered every two days, and the mixture to be cleaned has a molar composition of 47.6% IPA, 37.4% NPB, 7.5% oleic acid, and 7.5% water. The goals of the project are to completely remove the oleic acid, reduce the water molar composition to below 2.5%, maximize co-solvent recovery, and maximize profitability.</p>
<p>A major challenge of the project is the non-ideal behavior of the components, which includes multiple azeotropes and distillation boundaries. Another important characteristic of this design project is the unusually small scale: one 6,240 gallon quantity of used co-solvent mixture must be processed every two days. Due to this scale, batch processes were investigated as well as continuous processes.</p>
<p>The continuous alternative utilizes three major separation units: a 15-tray distillation column, a decanter for the distillate, and an evaporator for the bottoms. 93.8% of the original IPA and 99.2% of the original NPB is recovered. There is no oleic acid and 0.5% by mole of water in the product. Pure NPB and IPA are added at the end of the separation to compensate for the lost co-solvents, and to restore the IPA/NPB ratio to 56/44. A $0.45/lb selling price of reclaimed co-solvent returns an IRR of 45.6% and an NPV of $2,657,300 in year 10 of production.</p>
<p>The batch alternative utilizes a batch distillation column with multiple receivers and recovers 95.4% of the original IPA and 99.7% of the original NPB. There is 0.8% water by mole and no oleic acid in the product. Pure NPB and IPA also must be added to restore the original ratio. Because the composition of water is higher in the batch product than in the continuous, the co-solvent mixture is sold at a lower $0.42/lb, resulting in an IRR of 37.2% and an NPV of $2,452,500 in year 10. However, the batch process has significant down time and can potentially handle up to four times the solvent demand (2 trucks of solvent/day), resulting in an IRR of 130% and an NPV of $22,494,500 at the same selling price. Because of the batch plant’s ability to handle demand growth, its flexibility in separating different co-solvent ratios, and its robust economic potential, we recommend the construction of the batch co-solvent reclamation plant.</p>

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<author>Haoyu Deng et al.</author>


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<title>Renewable Acrylic Acid</title>
<link>http://repository.upenn.edu/cbe_sdr/37</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/37</guid>
<pubDate>Mon, 20 Aug 2012 11:36:51 PDT</pubDate>
<description>
	<![CDATA[
	<p>Acrylic acid is an important industrial chemical, used as a raw material in a wide variety of consumer end products. The present predominant source of acrylic acid is from the partial oxygenation of propene, produced as a by-product in the industrial production of ethylene and gasoline. Both processes depend heavily on the processing of petrochemicals as the base raw material. The purpose of this process is to produce acrylic acid from renewable carbon sources (such as corn or sugarcane) in an economically preferential manner. Our process has used genetically recombinant <em>Escherichia coli (E. coli) </em>to ferment the carbohydrate content of the proposed feedstock to 3-hydroxypropionic acid (3-HP) which is then dehydrated in the presence of strong acid catalyst (phosphoric acid) to form acrylic acid. The acrylic acid is then purified to the standard required for use as a polymer raw material (99.98% by mass) with total capacity of 160,000 MT/year of product.</p>
<p>This design analyzes two proposed locations, the US Midwest or Brazil, and their associated renewable feedstocks, corn or sugarcane juice, respectively. This report investigates the relative economic attractiveness of each option. The US case requires location near an existing industrial ethanol fermentation plant to give easy access to dry-ground corn as a carbohydrate source. This case yields an IRR of 17.56% and an overall NPV of $35.2 million at a 15% discount rate. The Brazil case has comparatively cheaper feedstock, however because of seasonality and total usable carbohydrate content, it requires a greater mass of feedstock and increased capital investment relative to the US case. The NPV difference of the two cases is extremely sensitive to the assumed price of sugarcane juice which has recently shown extraordinary volatility. Based on this analysis, the US location seems most promising; however, detailed laboratory level studies are needed to confirm the profitability and assumptions made.</p>

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<author>Andrew Cie et al.</author>


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<title>Renewable Para-Xylene</title>
<link>http://repository.upenn.edu/cbe_sdr/36</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/36</guid>
<pubDate>Mon, 20 Aug 2012 11:36:49 PDT</pubDate>
<description>
	<![CDATA[
	<p>This report details a process designed to renewably produce 400 million pounds of para-xylene per year from corn dry grind, sugar cane molasses (SCM), or woody biomass while minimizing water use. The para-xylene should be suitable for the production of polymers and plastics, and should be economical and green. All three feedstocks are equally suitable for the process and available for use.</p>
<p>The process is designed for SCM and consumes a total feed of 9.35 billion pounds of molasses per year. Corn dry grind is simply too expensive, and biomass, while cheaper per pound, imposes too many additional pre-processing costs. The molasses first undergoes hydrolysis then hydrogenation, followed by condensation and separation involving distillation and crystallization. Transalkylation and aqueous phase reforming are also employed to boost yield and create a self-contained process.</p>
<p>Several key assumptions are inherent in this process’s design. First, all reactor yields come directly from specific examples in the literature. Second, results found in the patents for glycerol were assumed valid for sorbitol as well, since not all patents used the same materials for their examples. Third, the economic analysis assumes that raw materials for catalyst manufacture can be purchased in bulk for a quarter of the price for small quantities. This assumption was suggested by Dr. Fabiano.</p>
<p>Based on these assumptions, the process designed herein meets the desired non-financial criteria, but results in an investor’s rate of return of negative 2.90% and a net present value of negative $196 million. However, further research into the catalyst or reactor yields could easily allow the process to break even or offer an attractive return.</p>

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<author>Eric Castillo et al.</author>


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<title>THE DIAMOND HEMESEP BLOOD PROCESSING UNIT: A REAL-TIME MICROFLUIDIC WHOLE BLOOD SEPARATION PROCESS</title>
<link>http://repository.upenn.edu/cbe_sdr/35</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/35</guid>
<pubDate>Mon, 20 Aug 2012 11:36:48 PDT</pubDate>
<description>
	<![CDATA[
	<p>Recent advancements in the field of microfabrication and microfluidics have made possible the design of separation devices and clinical diagnostic kits that use relatively smaller volumes of sample material than existing technologies. Using this technology, as well as existing technologies in membrane and immunomagnetic separations, a novel blood processing unit based on microfluidics has been designed. This report will detail the operation and layout of a microfluidic chip that produces three outputs (serum, plasma and a white blood cell lysate) from a human whole blood input. Microfluidic technology has allowed for the design of several distinctive features that make the performance of the blood processing unit comparable to existing centrifuge technologies available clinically and in research laboratories. Among other features, the chip produces a stabilized white blood cell lysate and is designed to match the blueprint of existing 96-well plates. In addition to describing the on-board processes and features of the chip, this report will also discuss the components needed for operation of the chip as well as a process to manufacture the product.</p>
<p>This product, known as the Diamond HemeSep blood processing unit, could offer more standardized, efficient blood separation technologies that would benefit health care providers, patients and researchers. Moreover, the product is predicted to have a healthy financial outlook: based on the target market of clinical laboratories performing preclinical and clinical trials involving numerous samples of blood, we expect to sell 1 million cartridges in the first year of production with sales growing to 1.7 million cartridges in the tenth and final year. The net present value (NPV) of the proposed project, based on a selling price of $25 a cartridge, is expected to be $51 million. For the current projections, Series A investors can expect returns of 45%.</p>

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<author>Daniel Moonan et al.</author>


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<title>TWO-STEP PRODUCTION OF 1,3-BUTADIENE FROM ETHANOL</title>
<link>http://repository.upenn.edu/cbe_sdr/34</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/34</guid>
<pubDate>Mon, 20 Aug 2012 11:36:46 PDT</pubDate>
<description>
	<![CDATA[
	<p>A plant utilizing a two-step reaction process, which takes a 95% ethanol stream (by mass) and produces a 98% 1,3-butadiene stream, was designed for this project. The production goal for this plant was 200,000 tonnes of butadiene with the main motivation behind the project being the recent rise in butadiene prices. The process first passes ethanol through a catalytic dehydrogenation reactor to convert ethanol to acetaldehyde and hydrogen. A kinetic model was used to determine the reaction rates and operating conditions of the reactor. The acetaldehyde intermediate is further reacted with ethanol in a catalytic reactor to form butadiene. A hydrogen byproduct stream is also generated in this design and is purified for sale.</p>
<p>This report provides a design and economic analysis for the production of butadiene on the Gulf Coast. Process flow sheets, energy and utility requirements, and equipment summaries are provided and analyzed. Process profitability is sensitive to the cost of both ethanol and butadiene. It is shown that the plant is very profitable for its expected 15-year lifespan with an expected internal rate of return of 40%, return on investment of 34%, and net present value of $172,000,000 (for a discount rate of 15%). The process becomes unprofitable if the price of ethanol increases to over $3.00/gallon. A combination of increased ethanol price and decreased butadiene price will also cause the plant to be unprofitable. Therefore, plant construction is only recommended given an acceptable price of ethanol and butadiene.</p>

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<author>Jonathan Burla et al.</author>


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<title>Membranes for Olefin Separations</title>
<link>http://repository.upenn.edu/cbe_sdr/33</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/33</guid>
<pubDate>Mon, 20 Aug 2012 11:36:45 PDT</pubDate>
<description>
	<![CDATA[
	<p>Polymer grade propylene (99.5wt% propylene, 0.5wt% propane) is in high demand because it is used to produce polypropylene, which is used in many industry applications. Polymer grade propylene can be purified either from chemical grade propylene (93wt% propylene, 7wt% propane) produced by a steam cracker reactor or from refinery grade (35wt% propylene, 65wt% propane) propylene produced from a propane dehydrogenation reactor. The conventional distillation separation processes is expensive and energy intensive. This report attempts to explore membrane-only and hybrid systems as possible alternative paths to achieving the desired product purities.</p>
<p>A separations process incorporating a membrane presents a unique opportunity for our company to penetrate the market for olefin separations. Possible membrane separation processes include a membrane-only separation process and a hybrid system, the latter consisting of both membranes and distillation columns. The costs and benefits of each process were analyzed to determine the price of the membrane that would make a membrane separation process competitive. More specifically, the conventional distillation processes were examined as base cases to establish the target internal rate of return. Then the price of membrane that would yield the same IRR as the conventional distillation process was calculated for both membrane only and hybrid processes in each of the three cases below. For each of the three cases below, the conventional distillation separation process was established as the base case while the membrane only separation process and the hybrid system were explored as alternatives.</p>
<p>The cases below represent the feed and product combinations desired for the various separation processes that were explored.  <ul> <li><strong>Case A: </strong>Chemical grade (93%) to polymer grade (99.5%) propylene, with the chemical grade propylene feed coming from a steam cracker</li> <li><strong>Case B: </strong>Refinery grade (35%) to polymer grade (99.5%) propylene, with the refinery grade propylene feed coming from the propane dehydrogenation process</li> <li><strong>Case C: </strong>Refinery grade (35%) to chemical grade (93.0%) propylene, with the refinery grade propylene feed coming from the propane dehydrogenation process</li> </ul></p>
<p>After examining the three cases, the hybrid system was not considered a viable option for separation in case B and case C. The price of the membrane is obtained when the IRR of the membrane only and/or hybrid process are equal to that of conventional distillation. The price of the membrane was determined to be in the price range of $47-52/m<sup>2</sup>. This price was capped at the lowest membrane price calculated for any process ($52), for reasons explained in detail in the Conclusion. However, the membrane product must be priced lower than $52, because the IRR of a membrane process must be higher than that of conventional distillation in order to give our clients a compelling enough reason to adopt our membrane technology.</p>

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<author>Diya Li et al.</author>


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<title>MICROFLUIDIC PRODUCTION OF DEPO-HALOPERIDOL WITH A CONTROLLED RELEASE PROFILE</title>
<link>http://repository.upenn.edu/cbe_sdr/32</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/32</guid>
<pubDate>Mon, 20 Aug 2012 11:36:43 PDT</pubDate>
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<author>William Mulhearn et al.</author>


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<title>ALGAE TO BIODIESEL</title>
<link>http://repository.upenn.edu/cbe_sdr/31</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/31</guid>
<pubDate>Tue, 24 Jul 2012 11:44:44 PDT</pubDate>
<description>
	<![CDATA[
	<p>In the spring of 2010, a CBE 459 design team focused on cultivating algae with the SimgaeTM Algal Biomass Production System, extracting algal lipids using OriginOilTM single-step extraction technology, and converting lipids into green diesel fuel. It was determined that the process was profitable, but required a staggering capital investment of 2.8 billion dollars. In the past year, both public and private institutions have joined the race to produce biofuels from an algal feedstock in an economically responsible manner that is by maintaining profitability while minimizing high capital costs. The intention of this report is to contribute to the global discourse on alternative-fuels and to reevaluate the promise of algae as a renewable resource for alternative fuels in light of the latest research and technological advances.</p>
<p>The algae-to-biofuel venture was segmented into three modules: algal cultivation, lipid extraction and lipid processing. Each module was studied thoroughly and several strategies were proposed for the reduction of its associated fixed, capital and variable costs. As contrasted with a previous study, it was concluded that heterotrophic algal cultivation and transesterification lipid- processing technologies would improve the efficiency and reduce the total capital investment. Once each module was designed in detail, the three segments were stitched together to perform an overall economic analysis. Based on the current market price of $3.30 per gallon for pure biodiesel, a project life of 15 years, and a 15% discount rate, the results indicate that an algae-to- biodiesel process may not only be profitable, but also a sound and reasonable investment. The project’s projected Net Present Value (NPV) is $1.3 billion and the Return on Investment (ROI) was determined to be 32%.</p>
<p>Although these economic results are promising, they are based on an analysis that necessarily invoked highly uncertain postulates in the dearth of published data. For example, the kinetics used to model the lipid-processing module were based on data collected for palm oil at similar conditions, while the details of lipid-extraction energy usage for a high-density slurry were approximated on the basis of results for low-density slurry. Furthermore, it was concluded that the income from the sale of the algal biomass byproduct of lipid-extraction is a critical factor in the profitability. Based on its protein content, this report considered the use of algal biomass as animal feed and determined its economic worth accordingly. However, to ensure the economic success of biodiesel production, an additional analysis should focus on algal usage of biomass as a feedstock and confirm the safety of its use. Further analyses could examine other potential applications for the byproduct, including opportunities within the pharmaceutical and power generation industries. Overall, in order to convince investors that the attractive economics published in this report may be translated into actual earnings, it is critical to move beyond modeling. Pilot studies must be conducted in order to bolster the proposed algae-to-biodiesel venture with experimental data and identify possible pitfalls.</p>

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<author>Daniel Choi et al.</author>


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<title>BIONOMER PILOT PLANT</title>
<link>http://repository.upenn.edu/cbe_sdr/30</link>
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<pubDate>Tue, 24 Jul 2012 11:44:37 PDT</pubDate>
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	<p>The purpose of this project is to develop a pilot-scale process for the bacterial production of methacrylic acid (MAA) and methyl ethyl ketone (MEK) from biomass feedstocks and the subsequent purification steps. The pilot plant will also be located on site at a sugar cane refinery in Brazil where the feedstock should be inexpensive and readily available. Although these sugar cane refineries only operate for 9 months each year, molasses can be stored so that the pilot plant runs year-round.</p>
<p>To obtain useful information about the feasibility and scalability of the process, 30 M kg/yr of each product will be produced. The products will be tested for purity and samples will be sent out to consumers to demonstrate the quality of the product. The MAA and MEK must be of the same purity generated by current commercial processes. The pilot plant will be designed in three major parts. The first part consists of the bacterial fermentors that are used to produce and scale up MAA and MEK production. Relatively little is currently known about the efficiency of production of MAA and MEK by <em>E. coli </em>and this part of the plant will provide critical data about conditions required for the bacteria as well as production rates. The second part of the plant consists of the MAA purification process. Many options will be considered for the purification steps, many of which will have to be modeled in ASPEN because MAA is usually not produced in the aqueous phase. The final section of the plant will be used for MEK purification. To reduce plant costs, the design will try to share equipment between the two purification processes.</p>
<p>The main goal of the plant is to obtain data and demonstrate feasibility, not to demonstrate sustainable profitability. Estimates for total capital investment and show that the plant will not be profitable for the first five years of operation, but the valuable data gained from the operation will be used to design the larger, more efficient, full-scale plant. The total capital investment required for the plant is approximately $ 6.33 million. Returns generated from sales are minimal compared to the capital investment and operating costs. A full scale plant is expected to be profitable over time because of economies of scale and the price of inputs and outputs of the process.</p>

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<author>Sifat A. Ahmad et al.</author>


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<title>MICRO$EC: Cost Effective, Whole-Genome Sequencing</title>
<link>http://repository.upenn.edu/cbe_sdr/29</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/29</guid>
<pubDate>Tue, 24 Jul 2012 11:44:36 PDT</pubDate>
<description>
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	<p>While the feasibility of whole human genome sequencing was proven by the success of the Human Genome Project several years ago, the prevalence of personal genome sequencing in the medical industry is still elusive due to its unrealistic cost and time requirements. <em>Micro$eq </em>is a startup company with the goal of overcoming these limitations by sequencing a minimum of 12 complete human genomes per day at an error rate less than ten parts in million at a profitable market price of less than US$1000 per genome. To overcome the technology bottlenecks hindering current biotech companies from achieving these target throughput, error rate, and market price goals, <em>Micro$eq </em>has developed an innovative sequencing technique that uses shortread fragments with high coverage on a microfluidics platform. Short, amplified DNA fragments are generated from an input of customer saliva. 6 base pair(bp) sequence hybridization is used for sequencing each of the DNA fragments individually. The results are these hydridization reads are then assembled via de Bruijn graph theory and the graphical reconstructions of each fragment’s sequence are then assembled to a complete genome via shotgun sequencing with an expected error rate less than 1 in 100,000bp. Upon the completion of financial analysis, both a small-scale business model producing 72 genomes per day at US$999 per genome, and a largescale business model producing 52.2 genomes per year at a market price of US$299 per genome were found to be profitable, yielding Micro$eq investors return margins of ~90% and 300% for the small and large scale models, respectively<em>. </em>With a market price <em>Micro$eq</em> offers personal genome sequencing at one-tenth of its nearest potential competitor’s cost. Additionally, its ability for bulk-sequencing allows it to profitably venture into the previously untapped Pharmaceutical Industry market sector, enabling the creation of large-scale genome databases which are the next step forward in the quest for truly personalized.</p>

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<author>Kulika Chomvong et al.</author>


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<title>Drinking Water Supply System using Solar Power</title>
<link>http://repository.upenn.edu/cbe_sdr/28</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/28</guid>
<pubDate>Tue, 24 Jul 2012 11:44:35 PDT</pubDate>
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	<p>The main objective of the project was to provide affordable and sustainable power to the water supply systems in Las Delicias, El Salvador and Apatut, the Philippines. The best fit for our system was determined to be a photovoltaic cell system. The PV solar technology was implemented in both project sites and is expected to provide the energy for all the water pump needs, which include 7.5 hp (5.625 kW) in Apatut and 34 hp (25.5 kW) in Las Delicias.</p>
<p>The current water supply system in Las Delicias consists of 75 hp (56.25 kW) pump system. It was determined that a re-design of the hydraulic system was necessary to reduce power requirements. The new design added a new holding tank and eliminated the need for a 60 hp booster pump, reducing the total pump power needs to 34 hp (25.5 kW). This design allows the villagers to receive continuous water. The total investment of this new design is $120,000 and yields a NPV of $413,000 (at 1.6% discount rate) and an IRR of 36%.</p>
<p>The system in Apatut is a grass roots project. We worked with the initial design provided by the EWB-MAP team that is currently involved with the project. The total investment is $22,000 and yields a NPV of $78,000 (at 1.6% discount rate) and an IRR of 41%.</p>

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<author>Renata Bakousseva et al.</author>


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<title>Electrical Energy Storage Using Fuel Cell Technology</title>
<link>http://repository.upenn.edu/cbe_sdr/27</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/27</guid>
<pubDate>Tue, 24 Jul 2012 11:44:34 PDT</pubDate>
<description>
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	<p>The goal of this project was to design three different energy storage systems utilizing reversible solid oxide fuel cells. Two of the systems use gaseous feed stocks and require storage for the gas produced by electrolysis. In the third design, molten antimony oxide is reduced to pure antimony during electrolysis rather than storing the energy in a gas. The three systems discussed in this report use electric power during off-peak demand hours to electrolyze a chemical feedstock. The resulting products are then stored for use during peak demand time in fuel cell operation. The systems were designed to store 1 MW of electrical power over a 12 hour period of off-peak demand and release power during a 12 hour period of peak demand. In the two gaseous systems, the fuel cell is made of an yttria-stabilized-zirconia (YSZ) electrolyte with porous nickel at the anode and YSZ-LaMnO<sub>3</sub> composite at the cathode.</p>
<p>In the electrolysis of steam to form hydrogen, the hydrogen is stored in pressurized vessels at 100 psi. During fuel cell mode, the hydrogen gas is oxidized in the fuel cell to form water, which is again stored for use in electrolysis the following day. The operating temperature for both electrolysis and fuel cell operation is 1472°F. The overall efficiency for the hydrogen system is 52.4%, with the main losses occurring as heat supplied to the electrolyzer.</p>
<p>The second design electrolyzes a mixture of steam to hydrogen and carbon dioxide to carbon monoxide at 1292°F and 147 psia. The resulting syngas is fed through a methanation reactor to produce a methane rich stream. The overall efficiency of the methane-based system is 55.7%, with the main losses coming from compression and heating for electrolysis mode.</p>
<p>The molten antimony fuel cell uses an equimolar mixture of antimony and antimony trioxide as the feedstock for electrolysis. The electric current in the electrolyzer reduces the antimony trioxide to form a stream of pure molten antimony. Both the electrolyzer and fuel cell operate isothermally at 1292°F and 14.7 psia. The overall efficiency for the antimony design is 53.7%, with the main losses coming from heat supplied to the electrolyzer.</p>
<p>For profitability analysis, off peak electricity was priced at $0.06/kWh and peak power was priced at $0.20/kWh. Under these optimistic assumptions, the return on investment (ROI) for the hydrogen design was calculated to be -26.1%. For the methane system, the ROI was calculated to be -19.2%. For the antimony case, the ROI was found to be -34.2%. These designs serve as a framework for future work with electrical energy storage. However, we believe that with improvements in system efficiency and reductions in the initial capital investment, future reversible fuel cell systems will be profitable and competitive with other forms of electrical energy storage.</p>

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<author>Erica Harkins et al.</author>


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<title>Glycerol to Propylene Glycol</title>
<link>http://repository.upenn.edu/cbe_sdr/26</link>
<guid isPermaLink="true">http://repository.upenn.edu/cbe_sdr/26</guid>
<pubDate>Tue, 24 Jul 2012 11:44:32 PDT</pubDate>
<description>
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	<p>A Cu-ZnO-Al<sub>2</sub>O<sub>3</sub> catalyst has been observed in laboratory scale tests to effectively produce propylene glycol from glycerol using a liquid phase hydrogenolysis reaction, which occurs at 410 F and 580 psia. A trickle-bed reactor will be used to ensure the full contact of liquid and vapor phases with the solid catalyst. This project aims to successfully scale up this reactor model, which has thus far only been tested in bench scale. The design specification stipulates that this process will produce 100 MM lb/year of propylene glycol. Using crude glycerol harvested from biodiesel production, a final product purity of 99.6% was achieved from a feedstock of 80% glycerol, 15% water, 1% methanol, and 4% sodium chloride by weight, plus trace amounts of organic salts.</p>
<p>The economic analysis that follows assumes a grassroots plant on the US Gulf Coast. The total capital investment was calculated to be $34.0 million, which includes a working capital of $9.78 million. Under the assumptions that the prices of crude glycerol, hydrogen, and propylene glycol are $0.22, $0.50, and $1.00 per pound respectively, the net present value (NPV) at the end of the 15 year allotted course of the project is $88.4 million and the investors’ rate of return (IRR) is 58.45%. The price of glycerol is projected to remain stable or decrease in the future and the price of propylene glycol is projected to remain stable or increase suggesting that this project could become even more profitable in the future.</p>
<p>The apparent profitability of this project is largely caused by the efficient and cost effective method of desalting glycerol through electrodeionization. Unfortunately, the proprietary nature of this new process precludes public access to true costing and specifications for the equipment since firms as Dow largely control the technology. Thus, conservative estimations were made in our economic analysis to account for this uncertainty.</p>

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<author>Kumar Chatterjee et al.</author>


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