Page |1 Simulation of Methanol Production from Synthesis Gas Dr. Ruhul Amin, Imran Hassan, Avijit Das, RabetaYeasmin, Taslima Rahman, Tania Hossain Department of Chemical Engineering Bangladesh University of Engineering and Technology, Dhaka-1000, Bangladesh. Abstract An innovative process scheme to produce methanol from carbon monoxide and carbon dioxide is here presented and accessed via simulation.In this configuration, the synthesis gas stream, composed by CO, CO2, and H2 and fed to the methanol synthesis reactor, is produced by means of a reverse-water–gas-shift by which a CO stream is partially converted in carbon dioxide. A simulation model is applied to define the proper operating conditions to achieve synthesis gas composition targets. The simulation results show that the plant configuration represents a feasible way to produce methanol using carbon dioxide, competitively with the traditional process in which the synthesis gas is produced by a natural gas steam reforming unit.From the simulation, some graphs were plotted. These graphs showed the dependency of simulation on variables (temperature, pressure etc).This were useful to understand the changes that will occur if properties of each unit were changed. Since pilot plants are expensive for this type of case, HYSYS gives us an opportunity to observe and realize the plant and the process happening inside. From the plots, optimum conditions for methanol production are found to be reactor temperature 200-300oC, reactor pressure 40-50atm. Keywords: Methanol; Synthesis Gas; Production of methanol; Purification; Simulation; Recycling. Page |2 1. Introduction Methanol, also known as methyl alcohol, wood alcohol, wood naphtha or wood spirits, is a chemical with the formula CH3OH. Methanol acquired the name "wood alcohol" because it was once produced chiefly as a byproduct of the destructive distillation of wood. At room temperature, it is a polar liquid, and is used as an antifreeze, solvent, fuel, and as a denaturant for ethanol. It is also used for producing biodiesel via transesterification reaction. From paints and plastics, furniture and carpeting, to car parts and windshield wash fluid, methanol is a chemical building block used in making hundreds of products that touch our daily lives. Methanol is a light, colorless, flammable liquid at room temperature, and contains less carbon and more hydrogen than any other liquid fuel. It is a stable biodegradable chemical that is produced and shipped around the globe everyday for a number of industrial and commercial applications. Methanol occurs naturally in the environment, and quickly breaks down in both aerobic and anaerobic conditions. The methanol industry spans the entire globe, with production in Asia, North and South America, Europe, Africa and the Middle East. Worldwide, over 100 methanol plants have a combined production capacity of about 100 million metric tons (33 billion gallons or 125 billion liters), and each day more than 180,000 tons of methanol is used as a chemical feedstock or as a transportation fuel (60 million gallons or 225 million liters). The global methanol industry generates $36 billion in economic activity each year, while creating over 100,000 jobs around the globe. Methanol is produced naturally in the anaerobic metabolism of many varieties of bacteria, and is commonly present in small amounts in the environment. As a result, there is a small fraction of methanol vapor in the atmosphere. Over the course of several days, atmospheric methanol is oxidized with the help of sunlight to carbon dioxide and water. [1] In a typical plant, methanol production is carried out in three steps. The first step is to convert the feedstock natural gas into a synthesis gas stream consisting of CO, CO2, H2O and hydrogen. This is usually accomplished by the catalytic reforming of feed gas and steam. Partial oxidation is another possible route. The second step is the catalytic synthesis of methanol from the synthesis gas. Each of these steps can be carried out in a number of ways and various technologies offer a Page |3 spectrum of possibilities which may be most suitable for any desired application. And, the final step is distillation of the final product to obtain required product specification. [2][4] Computer based simulation has been popular now-a-days for different chemical engineering purposes. Though our task was to represent production of methanol in renowned aspen HYSYS software, making some assumptions and using hypothetical reactors we have performed the methanol production simulation. Though it does not give the real world performance or the real life production environment, but it can give relief from making wide range of experiment without making the small scale reactors or plant. Here, a short literature review of methanol synthesis and its kinetics and modeling is presented. The simulators for the process are developed based on the models from the literature. The simulators are used to evaluate the steady state behavior of the process even though the mutual agreement about the reaction mechanism has not been established and thus the reliability of the results cannot be evaluated. The evaluation of the results will be carried out later when the applicability of the models found from the literature will be studied with the process data. Page |4 2. Methodology 2.1 Process Description The process chain for producing methanol is rather simple including the following phases • Production of synthesis gas • Conversion of synthesis gas to methanol and • Distillation of the final product to obtain required product specification. [3] 2.2 Production of synthesis gas Synthesis gas is a fuel gas mixture consisting primarily of hydrogen, carbon monoxide, and very often some carbon dioxide. CO, CO2 and H2 produced from various sources through steam reforming, partial oxidation, CO2 reforming or auto thermal reforming [Lovik 2001]. Originally, synthesis gas for the production of methanol came from coal. Today, synthesis gas is most commonly produced from the methane component in natural gas, because natural gas contains hydrogen. Three processes are commercially practiced. At moderate pressures of 4 MPa (40 atm) and high temperatures (around 850 °C), methane reacts with steam on a nickel catalyst to produce synthesis gas according to the chemical equation: CH4 + H2O → CO + 3 H2 This reaction, commonly called steam-methane reforming or SMR, is endothermic, and the heat transfer limitations place limits on the size of and pressure in the catalytic reactors used. Methane can also undergo partial oxidation with molecular oxygen (at atmospheric pressure) to produce synthesis gas, as the following equation shows: 2 CH4 + O2 → 2 CO + 4 H2 This reaction is exothermic, and the heat given off can be used in-situ to drive the steam-methane reforming reaction. When the two processes are combined, it is referred to as autothermal reforming. The high pressures and high temperatures needed for steam-reforming require a greater capital investment in equipment than is needed for a simple partial-oxidation process; however, the energy-efficiency of steam-reforming is higher than for partial-oxidation, unless the waste-heat from partial-oxidation is used. [5][6] In methanol synthesis, either CO or CO2 or both hydrogenates to methanol. The reactions are [Klier 1982] Page |5 CO + 2H2↔CH3OH (1) CO2+ 3H2 ↔CH3OH + H2O (2) Also the water gas shift reaction may occur [Skrzypek 1995].The water gas shift reaction is CO + H2O → CO2 + H2 (3) [7] The production of methanol is strongly influenced by thermodynamics. The thermodynamic equilibrium limits the process to a low conversion and thus the recycling of the outlet is required if a high conversion is desired. The overall reaction is also strongly exothermic and thus a significant cooling is required. The recycling and the cooling are the main causes of the investment costs. The methanol synthesis reactors have been designed based on three principlesthe high cooling demand, the low pressure drop and the favourable economy of scale. [Lange 2001]. Equilibrium constant of reactions depend largely on temperatures. For equation (1) equilibrium constant vs. temperature graph is shown below: Table 01: Variation of equilibrium constant of reaction 1 with temperature Keq 1 4574 20.5 0.349 1.44E-02 1.11E-03 1.34E-04 2.29E-05 5.09E-06 1.40E-06 4.54E-07 1.70E-07 7.11E-08 3.28E-08 1.64E-08 8.80E-09 Keq 1 vs Temperature 5000 4000 3000 Keq Temperature(°C) 37.8 93.3 148.9 204.4 260 315.6 371.1 426.7 482.2 537.8 593.3 648.9 704.4 760 815.6 2000 Keq 1 1000 0 0 500 1000 -1000 Temperature (°C) Figure 01: Keq1 vs. Temperature plot Page |6 For equation (2) equilibrium constant vs. temperature graph is shown below: Table 02: Variation of equilibrium constant of reaction 2 with temperature Keq 2 9.12E-02 4.52E-03 4.46E-04 7.00E-05 1.53E-05 4.27E-06 1.44E-06 5.65E-07 2.49E-07 1.21E-07 6.40E-08 3.62E-08 2.17E-08 1.37E-08 8.98E-09 1.00E-01 8.00E-02 6.00E-02 Keq 2 Temperature(°C) 37.8 93.3 148.9 204.4 260 315.6 371.1 426.7 482.2 537.8 593.3 648.9 704.4 760 815.6 4.00E-02 Keq 2 2.00E-02 0.00E+00 0 -2.00E-02 500 1000 Temperature (°C) Figure 02: Keq2 vs. Temperature plot The production of methanol from synthesis gas may take place under the low or high pressure. The high pressure process operates typically at 200 atm and 350°C while the low pressure process operates at 50 - 100 atm and 220 - 250°C. The low pressure process has such economical and operational benefits that almost all the methanol plants built after year 1967 operate at the low pressure. [Klier 1982] [9] Page |7 Some of the units used in HYSYS are given below: Mixer: Mixes two or more fluid stream input and gives one output. Heater: This unit heats up the feed to desired temperature by specifying the pressure drop and outlet pressure. Methanol synthesis reactor (MSR): It is an equilibrium reactor chosen from the library. It is used for the equilibrium reaction sets only. This reactor is valid both for exothermic and endothermic reactions. It is also possible to maintain a constant temperature in the reactor by removing or supplying heat. Cooler: It is used to cool the process stream to desired temperature. Separator: It is used for separating liquid and vapor mixture in given process stream at a constant temperature or by inputting or removing heat. It is also possible to add reaction sets here. Distillation column: It is the most versatile tool in HYSYS. Any kind of distillation is possible in this unit. It works by separating most volatile components from a process feed. [8] Page |8 Page |9 3. Result and Discussions After performing the simulation we have found that the production of methanol (purity and production rate) depends on different parameters of the process. So by controlling these parameters optimum methanol production can be obtained. [11] From the simulation result we have observed the effect of several parameters on production. Those effects are described in below3.1 Purity of methanol on Feed stage to distillation The relation between composition of methanol in final product and feed stage to distillation can be easily realized from the table and plot given belowTable 03:Variation of purity of methanol with feed stage. Composition (%) 94 1 87.2328 93 2 89.5223 92 3 91.1117 4 92.2185 5 92.9683 6 93.4376 7 93.618 87 8 93.5038 86 9 92.9323 10 90.3068 Composition(%) Feed Stage 91 90 89 88 0 1 2 3 4 5 6 7 8 9 10 11 Feed Stage Figure03: Composition of methanol in product versus feed stage of distillation. From the table and plot, it is observed that purity of methanol increases in higher feed stage from top and reaches at maximum and then again decreases. For this synthesis, optimum feed stage is 6th stage. 3.2 Conversion of CO and CO2 on reactor feed temperature Conversion of both carbon monoxide and carbon dioxide both decrease with temperature increase. [10] But reaction rate will be low at low temperature. Considering these two opposite aspects, the reaction is done in 200oC. These phenomena can be easily observed from the table and the plot given below- P a g e | 10 Table 04: Variation of conversion of CO and CO2 with reactor feed temperature. Conversion of CO (%) 0.1802 Conversion of CO2 (%) 3.306 15 2.997 6.997 20 5.052 9.505 25 6.51 11.54 30 7.662 13.27 35 8.624 14.8 40 9.245 15.95 45 9.245 15.95 90 80 70 Conversion(%) Reactor feed pressure(atm) 10 60 Conversion CO 50 Conversion CO2 40 30 20 10 0 -10 0 50 100 150 200 250 300 350 400 450 500 Reactor feed temperature (ºC) Figure04: Conversion versus reactor feed temperature 3.3 Purity of distilled methanol on fraction of recycle Purity of methanol increases with increase in fraction of recycle. But there may be inert in the feed and to control the buildup of inert in the product, some reactor outlet has to be purged after separation and before recycle. Reactor feed pressure(atm) 10 Conversion of CO (%) 0.1802 Conversion of CO2 (%) 3.306 15 2.997 6.997 20 5.052 9.505 25 6.51 11.54 30 7.662 13.27 35 8.624 14.8 40 9.245 15.95 45 9.245 15.95 . Composition of Methanol (%) Table 05: Variation of purity of methanol with fraction of recycle. 93.6 93.4 93.2 93 92.8 92.6 92.4 92.2 92 91.8 0 0.2 0.4 0.6 0.8 1 Fraction of Recycle Figure 05: Composition of methanol in product versus fraction of recycle. P a g e | 11 3.4 Conversion of CO &CO2 on Feed pressure Conversion of both CO and CO2 increases with feed pressure i.e. reactor pressure. But considering the safety purpose and operational cost, optimum pressure is chosen at 39.48 atm. Reactor feed pressure(atm) 10 Conversion of CO (%) 0.1802 Conversion of CO2 (%) 3.306 15 2.997 6.997 20 5.052 9.505 25 6.51 11.54 30 7.662 13.27 35 8.624 14.8 40 9.245 15.95 45 9.245 15.95 Conversion(%) Table 06:Variation of conversion of CO and CO2 with reactor pressure. 18 16 14 12 10 8 6 4 2 0 Conversiom of CO Conversion of CO2 0 10 20 30 Pressure (atm) 40 50 Figure 06: Conversion of CO and CO2 versus reactor pressure 3.5 Purity of methanol on separator feed temperature Distilled methanol purity increases with increase in separator feed temperature. But after a certain temperature, it becomes constant. Table 07: Variation of composition of distilled methanol with separator temperature. Comp of distilled methanol (%) 91.338 92.1072 92.4105 92.834 93.1935 93.4369 93.592 93.6192 93.6351 93.6634 94 Composition(%) Separator Temperature (°C) 10 20 30 40 50 60 70 80 85 86 93.5 93 92.5 92 91.5 91 0 50 Separator temperature (°C) 100 Figure 07: Composition of distilled methanol versus separator feed temperature. P a g e | 12 3.6 Methanol production rate on reactor feed temperature Methanol production rate decrease with increase in reactor feed temperature. Temperature,(°C) 25 Production flow rate, (kgmole/hr) 222.7 50 217 100 204.6 150 186 200 161 250 125.2 300 75.89 350 30.06 400 5.32 430 0.6258 Methanol production rate(kmole/hr) Table 08: Variation of methanol production with reactor feed temperature. 250 225 200 175 150 125 100 75 50 25 0 Methanol production rate vs. reactor feed temperature 0 50 100 150 200 250 300 350 400 450 500 Reactor feed temperature(ºC) Figure 08: Methanol production rate versus reactor feed temperature. 3.7 Methanol production rate on Feed pressure Methanol production rateincreases with feed pressure i.e. reactor pressure. But considering the safety purpose and operational cost, optimum pressure is chosen at 39.48 atm. Pressure of Feed (atm) 10 15 20 25 30 35 36 37 38 39 40 Production Rate (kmole/hr) 65.16 142.9 174.2 191.1 203.4 211.3 212.9 216.2 213.7 216.6 217.1 Production Rate (Kmole/Hr) Table 09: Methanol production rate with reactor pressure. Production Rate vs. 250 Feed Pressure 200 150 100 50 0 0 20 40 Feed Pressure (atm) 60 Figure 09: Methanol production rate versus feed pressure. P a g e | 13 4. Conclusion Methanol synthesis is an important chemical process. In our paper, we have generated data based on the simulation performed in HYSYS. This data can help us understand the process in different situation in industrial practice. By varying the different parameters in this simulation environment, the effects of these parameters on methanol production are observed and the results are shown in graphical and tabular form. Using the plots, the optimum conditions for methanol production can be easily found out. P a g e | 14 References 1. Kurtz M., Wilmer H., Genger T., Hinrichsen O. and Muhler M. (2003) Deactivation of supported copper catalysts for methanol synthesis. Catalysis Letters, vol. 86, p. 77-80. 2. Lange J.-P. (2001) Methanol synthesis: a short review of technology improvements. Catalysis Today, vol. 64, p. 3-8. 3. 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