Small Scale GTL (STG Plus) Plant

Small Scale GTL (STG Plus) PlantCourse intrinsic Gas Processing engineering (ENCH 609, Winter 2017) drift TITLEGTL Syn fellate to Gasoline (STG Plus)Professor Dr. Nashaat NassarList of figures and tablesFig 1. Schematic sketch of the STG+ system (from Primus unripe Energy TM) .. (6)Fig 2. Sensitivity Analysis for case 62.5 MMSCFD (14) send back 1. Economic Indicators for invent evaluation (Detail calculation in Appendix).. (15)AppendixFig 1. Operating GTL plants on the world map The Oil Gas Year, 2015 . (21)Fig 2. example flow chart developed for the project (from Aspen plus V 7.2 Microsoft Visio 2010) (22) display panel 1 Used compounds and Values of yields for nuclear reactor 4 in the pattern . (19-20)Table 2 Economic Evaluation for case 1 10 MMSCFD ..(23)Table 3 Economic Evaluation for Case 2 62.45 MMSCFD (24)Table 4 push-down list balance of streams 1-22 for Case 1 10 MMSCFD .(25-26)Table 5 Mass balance of streams 1-22 for Case 2 62.45 MMSCFD .. (27-28)AbstractThe worlds energy demand is growing exponentially and to meet this demand, bringing new supply sources to the market is extremely critical. Natural gas resources atomic number 18 plentiful, geographically diverse and currently overly the cleanest burning dodo give the sack. Gas to Liquids (GTL) is a chemic act that transforms subjective gas or other gaseous hydro coulombs into towering quality liquid products that would otherwise be produced from naive oil Shell Global. GTL creates an additional opportunity to monetize a countrys resource of rude(a) gas by turning them into mellow quality liquid force come knocked out(p)s. GTL products argon colorless and odorless hydrocarbons with very low level of impurities.The purpose of this project is to simulate a small scale GTL (STG Plus) plant that transposes 10 MMSCFD of rich-methane natural gas into 672 gun barrel/day of gasoline. The first step of the STG Plus mould is called move reforming and it consists of the reaction betw een the methane in the natural gas with abundant water. The second step of the growth is the reaction between the hydrogen, and the carbon monoxide producing methanol. The methanol thus formed pass on be converted to dimethyl ether (DME) and finally, the DME impart be dehydrated, producing gasoline. The project lead also highlight the difference between two major GTL technologies Fischer Tropsch and STG Plus. An economic evaluation was conducted to check the viability of this process and at 10 MMSCFD conversion of methane the project proves to be economically profitable, with an NPV value of $14.66M at 10% discount rate. It was also determined that if the merchandise of gasoline increases to over 4,100BBL/day, the profitability of this project will increase significantly.1.0. Introduction 1.1. GTL Technology and the WorldGasoline to Liquid (GTL) is a technology that converts natural gas or other gaseous hydrocarbons into high quality liquid products like gasoline or diesel moto r fuel, otherwise produced from unsmooth oil . GTL products are colorless and odorless hydrocarbons with very low level of impurities. Refineries can also use GTL to convert some of their gaseous hydrocarbon waste products into valuable fuel oil which can be used to generate income.The worlds first commercial GTL plant was opened by Shell in Bintulu, Malaysia in 1993. In 2011, the largest GTL plant, Pearl GTL was opened in Qatar Shell Global. Figure 1 in the Appendix shows all operating GTL plants and their turn backing locations on the world map.1.2. GTL OriginIn 1920s, when Germany found itself short of petroleum but with ample reserves of coal, GTL and Coal-to-Liquids (CTL) technologies were pioneered using a process known as Fischer-Tropsch (F-T) discount (Heng et al. 2004). Methanol-to-gasoline (MTG), Mobils synthetic gasoline process, establish on the transformation of methanol to hydrocarbons using zeolite accelerator pedals, was the first major synfuel process developmen t in half a deoxycytidine monophosphate since the development of the Fischer-Tropsch process (Frerich J. Keil, 1998).1.3. Gas-to-Liquid (GTL) technologyGas to Liquids (GTL) is a refinery process that converts gas or other gaseous hydrocarbons into products with longer carbon chains. Gasoline and diesel fuel are classic examples. Gases with a high concentration of methane are transformed into liquid synthetic fuels chase two methods direct transformation using processes without the front man of catalysts that convert methane to methanol or by using syngas as a midway product, such as in the Fischer Tropsch, Syngas to Gasoline Plus and Mobil processes.This project will focus on designing a small scale Syngas to Gasoline (STG) plus plant that uses methane rich natural gas as render and converts it to high quality gasoline and other products.2.0. Syngas-to-Gasoline plus (STG+) processSTG+ process was derived from the MTG (Methanol-to-Gasoline) process, which was developed by Mobil in the 1970s. This technology directly converts natural gas-derived syngas into drop-in gasoline and jet fuel through a catalytic thermo-chemical single-loop process that minimizes complexity, improves product quality and yield. The plus in STG+ stands for the alternate end products yielded by the process.The STG+ technology is currently operating by Primus commons Energy company in Hillsborough, New Jersey at pre-commercial scale with a production of 100,000 gallons (approximately) of distinct quality gasoline per year from natural gas with surpassed performance of the STG+ system and catalyst and 720 hours of continuous operation. The STG+ process consists of the following operating steps in one continuous process loop. It comprises of Syngas generation by move reforming method, four fixed bed reactors in series and a two phase separator.Figure 1 Schematic sketch of the STG+ system (from Primus Green Energy TM)2.1. Syngas Generation by go reforming methodThe first step in the S TG+ process is to convert the natural gas feed into syngas or deductive reasoning gas which is an intermediate gas feed for many dissimilar petrochemical processes. This processing basically removes contaminants, such as mercaptans, sulfides, mercury and any others that can compromise the conglomerate catalysts performance that are used in the STG+ reactors before it is fed to the syngas generation unit. Either partial oxidation or steam reforming processes are used for syngas production.Steam reforming process is widely used to generate syngas for feedstock in different petrochemical processes. A mixture of hydrogen, carbon monoxide, carbon dioxide, and unconverted methane and steam are formed when methane reacts with steam in the presence of a catalyst such as Nickel or Rhodium at high temperature (800-1000 C), high pressure (20-40 bars) and steam-to-carbon ratio variable between 1.8 and 4 in the steam reforming process which is highly endothermic in nature (Mbodji et al., 201 2).The possible reactions areThe steam methane reforming reaction (SMR)CH4 + H2O CO + 3H2 H = +206 kJ mol-1 (strongly endothermic).. (1)The water-gas shift (WGS)CO + H2O carbon dioxide + H2 H = -41 kJ mol-1 (moderately exothermic) . (2)The product from the reformer depends on the operating pressure temperature, composition of the feed gas, and the proportion of steam fed to the reactor. The thermodynamics and kinetics of the reaction within the reformer decides the amount of carbon monoxide in the final product from the steam reformer (Larminie Dicks, 2000).2.2. Reactor 1 (Methanol Synthesis) outward-developing compressors are used to compress the syngas from reforming unit which enters the reactor 1 containing copper zinc as catalyst and the following reaction occurs.2H2 + CO CH3OH H = -92 kJ mol-1 .. (3) callable to the exothermic nature of the reactions, low temperatures favor conversion to methanol and pre- pepperinessing of the reactant gas and heating of the boiler feed water are done by this special heat. The position of the equilibrium depends on the pressure and temperature. The methanol formation is favored by increase in pressure.2.3. Reactor 2 (Dimethyl Ether (DME) Synthesis)After the crude methanol from reactor 1 is preheated, vaporized and then superheated between 300-320oC in a series of heat exchangers, it is then sent to the dimethyl ether (DME) reactor containing a dehydration catalyst (alumina) where methanol is partially dehydrated to an equilibrium mixture of DME, water and methanol which is a reversible and exothermic reaction.2CH3OH CH3OCH3 + H2O . (4)2.4. Reactor 3 (Gasoline Synthesis)In reactor 3, in presence of catalyst the product gas from reactor 2 converts to hydrocarbons including paraffins (alkanes), aromatics, naphthene (cycloalkanes) and olefins (alkenes), mostly from C6 to C10.2.5. Reactor 4 (Gasoline Treatment) To have high octane enumerate for synthetic gasoline and desirable volumetric properties, the product from reactor 3 is treated in reactor 4 to reduce the durene (tetra methylbenzene), Iso durene and tri methylbenzene components which have high freezing points.2.6. SeparatorFinally, in the reactor 4 two or three phase separation is done to obtain synthetic gasoline comprised of paraffins, aromatics and naphthene, non-condensed gas and water. The non-condensed gas is recycled back to the feed stream for reactor 1 and water is recycled back to the Steam Reformer (Syngas Generation Unit).3.0. Why STG+?The previous group answerable for GTL used the conventional GTL technology called Fisher Tropsh (FT) in their manakin process. Fischer-Tropsch (FT), which is a technology developed in early 1920s, converts gas into liquid hydrocarbons mainly diesel through a very complex process. While there have been significant improvements on the efficiency and technology of the Fisher-Tropsch process, the industry is in an urgent pauperization of new technologies capable of converting as much gas as pos sible into liquid fuels in a cheaper and more efficiently manner. As consequence, we decided to go for for our project the novel process called STG+ developed by Primus Energy. The main product of STG+ is gasoline as opposed to diesel. Since the most demanded liquid fuel in Canada, peculiarly in Alberta, is gas, we decided non use FT or any new technology producing diesel. STG+ has numerous advantages over the conventional GTL techniques such as bring low operating and peachy costs, higher production, better product quality and faster delivery times. The rival technology of STG+ is ExxonMobils MTG process. However, ExxonMobils MTG process has a greater environmental stupor and it is not very cost-effective. STG+ process was designed to correct some inefficiencies in the ExxonMobil process . The main correction is the integration of the reactors in a single-loop that increases the production and yields a higher quality of the gasoline with a less environmental impact A key exam ple is integration of the reactors in the STG+ process.4.0. Project Design/ salutary example4.1. Flowchart DescriptionThe lists of components that are considered in the simulation for the STG+ process and the yields in mass base for the one-quarter reactor (Keil, 2012) are shown in the Appendix (Table 1). The flow chart developed for the STG+ process is shown in the fig. 2 of Appendix.A brief explanation of the flowchart will be done now. First, our feedstock is basically the natural gas. For simplification purposes, our feed of natural gas is basically methane. Another feedstock that this process will have is fresh water. The water will be heated in a heat exchanger (HE-01) and will be mixed with the methane to enter the first reactor (R-01). In this reactor, carbon monoxide, carbon dioxide and hydrogen will be produced, as explained above. The fractional conversion in the first reaction is 83.4% of the methane, the limiting reactant. The conversion in the second reaction is 6% of the carbon monoxide (Choudhary et al, 1992). The exit stream of the reactor R-01 is cooled in a heat exchanger (HE-02), enters a compressor (CP-01) to increase the pressure for the second reaction process and, finally, enters another heat exchanger (HE-03) to adjust the temperature for the ideal temperature in reactor R-02. The operating conditions of this reactor are 69 bar and 380C (Wood et al, 2012). In it, basically, the syngas will be consumed to form methanol. The fractional conversion of this reaction is 63.7% of carbon monoxide (Lebarbier et al, 2012).The exit stream of reactor R-02 will pass through a heat exchanger (HE-04) to adjust the temperature of the mixture to enter reactor R-03. The methanol will form dimethyl ether (DME) and water. The operating conditions of this reactor are 12 bar and 325C (Wood et al, 2012). The fractional conversion of the methanol for this process is 76% (Kasaie et al, 2010).The stream that comes out of reactor R-03 passes through a heat ex changer (HE-05) to reduce its temperature and then enters a liquid-vapor flash vas (FV-01). The dimethyl ether along with the non-polar components will come out in the gas stream, while the water will come out in the substructure or liquid stream, which can be sent to the outflowing treatment plant. The gas stream will pass through a compressor (CP-02) and then through a heat exchanger (HE-06) to adjust the temperature and pressure for the fourth reaction process in reactor R-04. Basically, in this reactor, the dimethyl ether will be dehydrated in order to break down its molecule into -C2H4- radicals, which will be combined to form bigger molecules, as explained above. Since the reaction process is complex and the number of reactions is big, the stoichiometry of the process will be very complicated. at that placefore, this paper precisely shows the yield in mass basis of each component formed in reactor R-04 (yield per unit mass of total feed of components that are not listed a s inerts) (Aspentech Support Technology, 2001). Since only the dimethyl ether (DME) is a reactant in reactor R-04, all of the other compounds that enter reactor R-04 are considered inerts.The exit stream of reactor R-04 will pass through a compressor (CP-03) and through a heat exchanger (HE-07) to adjust the pressure and temperature for the last flash vessel (FV-02). This flash vessel is a liquid-liquid-vapor separator that will separate on the top the gas and lightest products. The middle liquid stream will be the gasoline formed (main stream) and the bottom liquid stream will be the water that was formed in the reactor R-04 and must be removed. The gas stream can be exchange to an industry that processes gas phase hydrocarbons, while the water removed can be sent to the effluent treatment plant.4.2. Thermodynamic Model and Simulation ConsiderationsThe simulation of the STG+ process was developed in the software Aspen Plus version 7.2. In our simulation, we chose the GRAYSON model , because it was developed for systems consisting of hydrocarbons, such as carbon dioxide and hydrogen sulfide. This method should return good results for temperatures in the range of 60F to 800F and pressures up to 3000 psia (Aspentech Support Technology, 2001). Since our process contains hydrogen and all the temperatures of the streams are within this temperature range, we can use the GRAYSON model (Aspentech Support Technology, 2001).The first three reactors (R-01, R-02 and R-03) were modeled in Aspen Plus as RSTOIC reactors since only fractional conversions and stoichiometry were considered for them. The last reactor (R-04) was modeled as an RYIELD reactor. In this model, the excitant data that is required consists of the outlet temperature and pressure of the reactor, as intimately as the yield values for the components that are products of the reaction process.4.3. Assumptions adopted in the simulation Natural gas feed consists only of methaneWe used only flash drums to perf orm the separation of the components after the reactions.The gasoline yields only consist of paraffins, olefins, aromatics and cyclic hydrocarbons from C2 to C11.Fractional conversions and stoichiometry are only considered for the first three reactors and no kinetic parameters for the reaction processes and catalyst deactivation are considered cod to lack of data.Even though the STG+ process is hearty known for the loop which defines the efficiency of the process, due to lack of data on fractional conversions for C2-C11 compounds, we restricted our simulation till gasoline production and planned to wander our product (Gasoline and Natural Gas) to the other parties who are in charge of any post treatment required.Since we are not including the durene/Isodurene in our output, the Gasoline treatment reactor is not considered.5.0. Economic EvaluationIn order to evaluate the economics of the project, a cash flow analysis is made based on the following considerationsOur business model consider buying treated natural gas to be used as both feedstock and fuel gas (we dont pay royalties because we are not producing it), paying for electrical energy consumption and revenues come from gasoline and natural gas sales.Two years for construction and 20 years of operations.340 days of production per year.Analysis in constant American dollars of January 2017, exchange rate of 1.30 CAD to USD.Annual non-fuel operating and maintenance cost equal to 3.6% (Haro P. et al ,2013) of total capital expenditures.Corporate income tax rate equal to 28%. electricity consumption, fuel gas required, flow rates (feed and products) from the simulation model.Current monetary values for gasoline, natural gas and electricity in Alberta, taken from Alberta Energy websites.Capital Cost Allowance (CCA) with a half year rule is considered for tax calculation purpose according to Alberta legislation. displace rate 10%.Capital expenditure (CAPEX) for syngas generation is estimated using figures for a known plant (Yang Ogden, 2005) and the following equation to take into account the different capacities. . (5)Where,Cx = capital cost for a plant of size x (Sx), Cb = capital cost of the known plant of size b (Sb).CAPEX related to the STG+ process itself is estimated based on the ratio given by Primus Green Energy (company proprietary of the STG+ technology) that syngas generation typically represents 60% of total capital cost for commercial-scale plant and the STG+ process itself represents the other 40%.Two scales are considered 10 MMSCFD of natural gas in the feed for comparison purpose with the previous years group and 62.5 MMSCFD of natural gas in the feed to evaluate the influence of the scale on the economic indicators.The economic indicators of the project are summarized in the following table commit Gas Flow rates (MMSCFD)1062.5Net Present Value NPV 10% (million $)14.66371.86Internal Rate of Return IRR12.12%22.87%Profit to Investment Ratio PIR0.140.97Breakeven price f or Gasoline (CAD/L)0.910.62Table 1 Economic Indicators for project evaluation (Detail calculation in Appendix)Finally, a sensitivity analysis is made to see the influence of different variables natural gas price, electricity price, gasoline price and capital cost on the NPV of the project. For these, all variables are changed +10% and -10% and the NPV are calculated. Results shown in the fig. 2 correspond to the case with 62.5 MMSCFD in the feed. However, it is the same trend in both casesFigure 2 Sensitivity Analysis for case 62.5 MMSCFDIt can be concluded that the project is economically feasible and the variable that impact the most the economics of the project is the gasoline price.6.0. RecommendationsWe recommend considering the fractional conversions for C2-C11 compounds in reactor 1 to have a better picture of STG+ with its close loop process.A thorough composition analysis for gasoline in the fourth reactor gives more realistic results.There is much scope to extend our work by adding gasoline treatment and distillation column (instead of flash drum for more efficient separation) with proper chemical reactions and stoichiometric fractional conversions and kinetics to improve the market value of our product.There is possibility for considering more components in the feed gas till C5-C6.In our model, due to lack of data, we focused on chemical reactions and stoichiometric fractional conversions. There is scope for more efficient designing by working on catalyst cycle life.7.0. ConclusionThe 21st century is witnessing the establishment of a new global business based on natural gas processing. As a consequence, the gas-to-liquids (GTL) industry is becoming increasingly important as it is getting more difficult to find and extract new oil reserves as well as the presence of more environmental restraints. This is why we decided to apply the new STG+ process technology in our project to demonstrate its efficiency in the conversion of methane to gasoline. As pr eviously stated, we decided to differ from the previous group process, mainly because its technology is old and their product is diesel as opposed to STG+ process which is a novel technology and its product being gasoline, which is more demanded in Canada. We chose to do the simulation of a small scale GTL plant that processes 10 MMSCFD of methane, producing 672 bbld, which resulted in an economically viable process. The economic indicators showed that, by increasing the production of gasoline, the profit would increase significantly (proven with the case 0f 62.5 MMSCFD). In conclusion, STG+ might be indeed prospered and profitable in Alberta if there is a reliable source of natural gas and good market conditions. 8.0. ReferencesAlberta energy website.http//www.energy.alberta.ca/NaturalGas/1316.asp. Accessed on March 16th, 2017.Alberta energy website.http//www.energy.alberta.ca/Electricity/679.asp. Accessed on March 16th, 2017.Aspentech Support Technology, Inc. Aspen Physical Prope rty System 11.1 Cambridge, MA, September 2001.Choudhary V. R., Rajput A. M., Prabhakar B Low temperature oxidative conversion of methane to syngas over NiO-CaO catalyst Chemical engineering Division National Chemical Laboratory, India, May 1992.Haro P, Trippe F, Stahl R, Henrich E. Bio-syngas to gasoline and olefins via DME A comprehensive Techno-economic assessment Apple Energy 2013 volume 108 page no. 54-65.Heng H.C., Idrus. S The proximo of gas to liquids as a gas monetization option diary of Natural Gas Chemistry 13, 2004 pages 63-70.http//www.albertagasprices.com/index.aspx?fuel=C . Accessed on March 16th, 2017.Kasaie M., Sohrabi M. energizing Study on Methanol Dehydration to Dimethyl Ether Applying Clinoptilolite Zeolite as the Reaction Catalyst Chemical Engineering Department, Amirkabir University of Technology, Tehran, Iran, January 2010.Keil, Frerich J. Methanol-to-hydrocarbons process technology Department of Chemical Engineering, practiced University of Hamburg-Harburg , Hamburg, Germany, July 1998 page 49.Larminie, James, Dicks, Andrew Fuel Cell Systems Explained West Sussex, U.K. John Wiley Sons 2000.Lebarbier V. M., Dagle R. A., Kovarik L., Adarme J. A. L., King D. L., Palo D. R. Synthesis of methanol and dimethyl ether from syngas over Pd/ZnO/Al2O3 catalysts Richland, USA, June 2012.Mbodji M., Commenge J.M., Falk L., Di Marco, Rossignol F., Prost L., Valentin S., Joly R., Del-Gallo P. Steam methane reforming reaction process intensification by using a milli structured reactor Experimental setup and model validation for global kinetic reaction rate estimation, Chemical Engineering Journal, vol. 207-208, pages 871-884.Primus Green Energy website (http//primusge.wpengine.com/press-room/white-papers/), Accessed in March 2017.Shell Global Website (http//www.shell.com/energy-and-innovation/natural-gas/gas-to-liquids.htm), Accessed March 05, 2017.Wood, David A., Nwaoha C., Towler, Brian F Gas-to-liquids (GTL) A review of an industry offering several routes for monetizing natural gas Journal of Natural Gas Science and Engineering, Volume 9, November 2012.Yang, Christopher Ogden, Joan M. (2005).Analyzing Natural Gas Based Hydrogen Infrastructure Optimizing Transitions from Distributed to Centralized H2 Production Institute of Transportation Studies UC Davis.9.0. Appendix portion in Aspen PlusComponent nameFormulaMass yieldMETHANEMethaneCH4-METHANOLMethanolCH4O-COCarbon monoxideCO-CO2Carbon dioxideCO2-H2OWaterH2O-ETHERDimethyl etherC2H6O-H2HydrogenH2-OCTANEn-OctaneC8H183.582HEXANEn-HexaneC6H142.702HEPTANEn-HeptaneC7H163.142NONANEn-NonaneC9H204.022DECANEn-DecaneC10H224.462N-C11n-UndecaneC11H2424.602N-C5n-PentaneC5H1236.078OXYGENOxygenO247.549ETHANEEthaneC2H64.901PROPANEPropaneC3H845.691N-BUTANEn-ButaneC4H1069.321ISOC4IsobutaneC4H10101.615ISOC52-Methyl-butaneC5H1275.269ISOC62-Methyl-pentaneC6H1434.921ISOC72,2-DimethylpentaneC7H163.137ISOC82,2-DimethylhexaneC8H181.690ISOC92-MethyloctaneC9H200.491ISOC102-MethylnonaneC10H2237.092ARO MC6BenzeneC6H64.024AROMC7o-XyleneC8H1