Design Of A Sulfuric Acid Production Plant Engineering Essay

Design Of A sulfuric Acid Production set Engineering EssayThis bulge out is prep ared according to the requirements of chemic engineering department, and its as well as a preliminary study of sulphuric venereal infection doing plant.The project begins with chapter one which includes introduction, definition of siemensic acerbic and shows the main uses of mental cropic pungent which have made it an important chemical in the world, followed by chapter two which negotiation about literature, market survey and the history and current adjoines for harvestion the sulfuric venomous also it gives small glimpse of the prices trends of the bare-ass material and product.That is followed by verbal description for various processes to produce sulfuric sultry in chapter three, which ends with the selection of the best process which is the double contact process the description and flow sheet of the selected process are discussed in chapter four.Material and energy balance resu lts are listed in chapter five and the location of the plant is selected in chapter six by comparing dissimilar locations, and the best location for the plant (as its set in this report) is Aqaba city. .Finally, material and energy balance details are discussed in the appendix, that includes the employ charts and references.CHAPTER ONEINTRODUCTION1.1 commentSulfuric acid is a strong mineral acid with the molecular produceula H2SO4. It is a clear, colorless, odorless, viscous bland that is very corrosive. It is soluble in irrigate at all concentrations. Sulfuric acid has m any applications, and is one of the top products of the chemical industry. on that point are another names for sulfuric acid, it is sometimes called crude oil of vitriol.1Its chemical formula is lick (1.1.1) Sulfuric Acid Formula11.2 Physical and Chemical propertiesThis table shows the main chemical and physical properties of sulfuric acidSulfuric acidIUPACOil of vitriolOther nameH2O4SMolecular formula98.08 g mol1Molar massClear, colorless, odorless unruffledAppearances1.84 g/cm3, liquid slow-wittedness10C, 283K, 50FMelting point337C, 610K, 639FBoiling pointMiscibleSolubility in water3Acidity(pka) acrid odorOdorNon-flammableFlash point26.7 cP (20 C)Viscosity0.3PhTable (1.2.1) physical properties11.3 Application and UsesSulfuric acid is a very important chemical commodity, and indeed, a nations sulfuric acid production is a good indicator of its industrial strength.It is employ as electrolyte in lead-acid batteries (accumulators) .It is important in the production of fertilizers such(prenominal) as ammonium sulfate (sulfate of ammonia), (NH4)2SO4, and superphosphate, Ca(H2PO4)2, which is organize when rock phosphate is treated with sulfuric acid.It is used to leave off oxides from iron and steel to begin with galvanising or electroplating .Concentrated sulfuric acid is used as a dehydrating agent, that is, to remove water, since it has a tendency to form hyd evaluate such as H2SO4 .H2O, H2SO4.2H2O.Sulfuric acid is used in the production of nitroglycerine, an inorganic ester organic nitrate, which is used as an explosive.It is used in petroleum refining to wash impurities out of fluffoline and other refinery products.It is used in manufacturing of hydrochloric acid, nitric acid, phosphoric acid, ether, plastics, metal sulfates, cellophane, dyes, drugs, perfumes, disinfectants and even glue.1This chart shows the distribution of using sulfuric acidFigure (1.3.1) Sulfuric Acid Distribution.1Specification of raw materialssulfur, S, 16Name, symbol, number32.065gmol1Standard atomic weightYellow colored lumps, crystals, powder, or formed shapeAppearancesLumps 75-115 lbs./ft3 Powder 33-80 lbs./ft3Bulk Density388.36K,115.21C,239.38FMelting point717.8K,444.6C,832.3FBoiling pointInsolubleSolubility In WaterSolidPhysical State1.819 gcm3Liquid density at maps.Table (1.3.1) Physical Chemical Properties of Sulfur.1CHAPTER TWOLITERATURE ANDMARKET SURVEY2.1 History and Curr ent processesThe discovery of sulfuric acid is credited to the 8th century che bedim and alchemist, Jabir ibn Hayyan (Geber). The acid was later studied by 9th century Persian physician and alchemist Ibn Zakariya al-Razi (Rhazes), who obtained the substance by ironical distillation of minerals including iron(II) sulfate heptahydrate, FeSO47H2O, and copper(II) sulfate pentahydrate, CuSO45H2O. When igniteed, these compounds decompose to iron(II) oxide and copper(II) oxide, respectively, giving off water and sulfur trioxide, which combine to produce a dilute solution of sulfuric acid. 1This method was popularized in Europe through with(predicate) translations of Arabic and Persian treatises, as well as books by European alchemists, such as the 13th-century German Albertus Magnus.1There are two major processes (lead bedchamber and contact) for production of sulfuric acid and it is available commercially in a number of grades and concentrations. The lead chamber process, the elder of the two processes, is used to produce ofttimes of the acid used to make fertilizers it produces a relatively dilute acid (62%-78% H2SO4). The contact process produces a purer, more concentrated acid but requires purer raw materials and the use of expensive particle accelerators. n both processes sulfur dioxide is oxidized and dissolved in water. The sulfur dioxide is obtained by keen sulfur, by burning pyrites (iron sulfides), by roasting nonferrous sulfide ores preparatory to smelting, or by burning hydrogen sulfide spoil. Some sulfuric acid is also made from ferrous sulfate waste solutions from pickling iron and steel and from waste acid sludge from oil refineries. 12.2 Supply and DemandThis table shows the production rates of sulfuric acid (in metric tones) in some countries at different years.Production of sulfuric acid in metric tonesYear arena1994199720002006France2227224222691755Germany3380349648984595Greece360675688815Italy1228159010431616Spain2348281024183500Unite d kingdom122512051058447Sweden5186306291010Table (2.2.1) Production Rates of Sulfuric Acid.3This table shows the production and sales amounts of sulfuric acid and the consumption rate of sulfur in Jordan from 2000 to 2005, these amounts in (ton/year).Sulfur consumption(ton/tear)Sulfuric acidYearSales(ton/year)Production(ton/year)3709254382411086052000309816466149195482001351011433071055208200226586551445961208200336430149661110289920043463454832310465402005Table (2.2.2)Jordan Production, Sales and Raw Material Consumption.52.3 Prices trends of the raw material and productThe global sulfuric acid market experienced an unprecedented rise and fall in pricing between fall 2007 and spring 2009. Consumption of sulfuric acid for fertilizers fell steeply in the back up half of 2008 due to the collapse in the global economy. The second half of 2009 is expected to experience around flat to slightly positive growth, anticipating the improvement in market conditions in 2010. Trade is expected to fall globally, except for Southeast Asia, which would continue to depend on imports. As of early spring 2009, the market is continuing to deteriorate as the supply shortage situation has been replaced by product oversupply in near all regions.And the world sulfuric acid supply trends are shown in the following chart.Figure (2.3.1) World Sulfuric Acid Supply.2CHAPTER THREEPROCESS picking functioning SelectionSulfuric acid is an important raw material used in many industrial processes, such as phosphate fertilizer production and to a much lesser extent for nitrogen and kilobyte fertilizers, sulfuric acid is produced by catalytic oxidation of sulfur dioxide to sulfur trioxide, which is afterwardward absorbed in water to form sulfuric acid.There are no major variations of commercial interests on this mentioned chemistry. There are alternatives as to beginning of Sulfur dioxide and method of conversion to sulfur trioxide. The two most common methods for the conversion of sulfur dioxide to sulfuricacid are1. Lead Chamber Process.2. get through Process3.1 Lead Chamber ProcessThis is an old process and was introduced in Europe in near the middle of 18th century, its used to produce much of the acid used to make fertilizers it produces a- relatively dilute acid (62%-78% H2SO4).The classic lead chamber process consists of three stages Glover towboat, lead chambers and Guy-Lussac Tower.In this method zesty sulfuric dioxide gas enters the bottom of the reactor called a Glover tower where it is wash with nitrous vitriol (sulfuric acid with nitric oxide, NO, and nitrogen dioxide, NO2, dissolved in it) and mixed with nitric oxide and nitrogen dioxide gases.The Glover tower serves two functions concentration of the chamber acid and stripping of nitrogen oxides from the liquid to the gas. Concentration of the chamber acid (62% to 68% H2SO4) is achieved by the hot gases entering the tower which evaporate water from the acid.Some of the sulfur dioxide is oxidized to sulfur trioxide and dissolved in the acid wash to form tower acid or Glover acid (about 78% H2SO4). The dissolved nitrogen oxides are stripped from the acid and carried with the gas out of the Glover tower into the lead chambers.From the acid tower a mixture of gases (including sulfur dioxide and trioxide, nitrogen oxides, nitrogen, oxygen, and steam) is transferred to a lead-lined chamber where it is reacted with more water.Sulfuric acid is formed by a complex serial publication of reactions it condenses on the walls and collects on the floor of the chamber. There may be from three to twelve chambers in a series. The acid produced in the chambers, often called chamber acid or fertilizer acid, contains 62% to 68% H2SO4.After the gases have passed through the chambers they are passed into a reactor called the Gay-Lussac tower where they are washed with cooled concentrated acid (from the acid tower) the nitrogen oxides and unreacted sulfur dioxide dissolve in the acid to form the nit rous vitriol used in the acid tower. remain waste gases are unremarkably action into the atmosphere.Product acid at a concentration of 78% H2SO4is drawn from the cooled acid stream that is circulated from the Glover tower to the Guy-Lussac tower. northward losses are made up with nitric acid which is added to the Glover tower.The major disadvantage includes the limitations in throughput, quality and concentration of the acid produced, also the environmental pollution.Figure (3.1.1) Typical process flow sheet for the lead Chamber.3.2 Contact ProcessBecause of economic reasons Contact plants are widely used compared to the lead plants, they are separate according to the raw materials charged to them elemental Sulfur burning, spent sulfuric acid and hydrogen sulfide burning, and metal sulfide ores and smelter gas burning. The contributions from these plants to the numerate acid production are 81, 8, and 11 percent, respectively.The contact process incorporates three basic operatio ns (stages), each of which corresponds to a distinct chemical reaction.First, elemental sulfur is received in a solid form containing various impurities. The sulfur is melted in the sulfur melter in the presence of hydrated lime which neutralizes any acidity present in the sulfur. This neutralization prevents problems of acid corrosion which would otherwise be encountered.Heat for the melting of the sulfur is supplied from steam coils. The molten sulfur is unploughed agitated to improve heat transfer, to prevent solids settling on the bottom of the sulfur pits and to prevent a crust forming on top. The dirty sulfur is filtered to remove impurities present and after filtering is transferred to the clean sulfur pit where it is kept molten until it is pumped to the burner.Molten sulfur at a temperature of 130C is sprayed into the burner in the presence of warm, dry air. The sulfur burns, forming sulfur dioxideS + O2 SO2 H = -300 kJ mol-1The resulting sulfur dioxide is fed to a proces s unit called a converter, where it is catalytically oxidized to sulfur trioxide (SO3)2SO2 + O2 2SO3 H = -100 kJ mol-1Its apparent that the equation gives a decrease in volume this reaction would be aided by cart. High conversions are however, obtainable with catalysts at 400 to 500oC with a small excess of oxygen and the use of pressure.The available methods to maximize the constitution of SO3As this is an exothermal process, a decrease in temperature by removal of the heat will favour the formation of SO3.Increased oxygen concentration.SO3 removal (as in the case of the double absorption process).Increased pressure.Catalyst selection, to subvert the working temperature (equilibrium).Longer reaction time.In the contact processes, the sulfur dioxide is converted to sulfur trioxide by the use of metal oxide catalyst, the characteristics of the used catalyst are holey carrier having large surface area, controlled pore size and resistance to process gases at high gear temperature in pellet form if used in improve bed andpowdered form if used for fluidized bed. Ex- Alumina, silica gel, zeolites.Active catalytic agentPreparations are world(a)ly kept secret for the competitive reasons but they usuallyconsist of adding water soluble compounds to gels or porous substrates and firingat temperature below the sintering point.PromoterAlkali and/or metallic compounds added in trace amounts to rise the activityof the catalytic agent.A catalyst, vanadium pentoxide (V2O5) is used to increase the reaction rate because its relatively immune to poisons, also because of its low initial enthronement and solitary(prenominal) 5% replacement per year. It is only effective above its melting point of 400 C. The greatest conversion of SO2 to SO3 is reached by passing the gas over several(prenominal) catalyst beds, cooling the gas between each pass so that the reaction temperature remains between 400 and 500 C. As can be seen the figure.The disadvantages of using the V2O5 cata lyst are that it must use dilute SO2 input (7-10%), as a catalyst it is less active and requires high oxygen or sulfur dioxide to give economic conversions also it requires larger converters and thus higher initial investment.Finally, the sulfur trioxide is absorbed in to very concentrated sulfuric acid (a 98-99 percent solution of H2SO4 in water), This operation takes place in the absorbing tower where the gas travels up through the tower, counter-current to the acid falling from the top of the tower producing a thick fuming liquid called oleum, the oleum is mixed carefully with water to avoid producing fine mist of sulfuric acid that is difficult to condense and could escape to stain the air, the sulfur trioxide in the oleum reacts with the water as followsSO3 + H2O H2SO4 H = -200 kJ mol-1It is clear that the reaction is exothermic and the absorbing sulfuric acid has to be cooled continuously the heat is available at a relatively low temperature and is not worth recovering.The ef ficiency of the absorption step is related to The H2SO4 concentration of the absorbing liquid. (98.5 99.5%).The temperature range of the liquid (normally 70 -120 0C).The technique of the acid distribution.The raw gas humidity (mist passes the absorption equipment).The mist filter.The temperature of incoming gas.The co-current or countercurrent character of the gas stream in the absorbing liquid.Main disadvantages of the contact process are that concentrated acid (98%) of high purity can be produced directly and that compact plants of quite high capacity have now become rather common place.The contact process can be applied in different techniques three of those techniques are described in the following sections3.2.1 Single contact / individual absorption processAfter purification and drying, the SO2 is converted to SO3 using a series of four catalyst beds, containing alkali and V2O5. Afterwards, the SO3 is absorbed in concentrated sulfuric acid and, if necessary, an oleum absorber is installed upstream. SO3 reacts with the water contained in the absorber acid to yield H2SO4. The absorber acid is kept at the craved concentration of approximately 99% w/w by addition of water or dilute H2SO4.The wiz contact/single absorption process is generally used for gases with an SO2 Content from 3 6 %. New single contact plants are built only for inlet gases with substantial fluctuation of the SO2 content.The investment cost of this technique is low compared to the investment cost of double contact plants.Figure (3.2.1.1) Typical process flow sheet for a single contact action plant.3.2.2 Double Contact/ Double Absorption ProcessThe double contact process was implemented to develop the single contact/single absorption process. In this process a primary SO2 conversion of 85 95 % is achieved in the first catalysis stage of the converter before entry into an intermediate absorber, depending on the arrangement of the converter beds and the contact time.What makes the doubl e contact/double absorption process more advantageous is that its ability to feed gases with higher SO2 concentrations than would be achievable with the single catalysis process. Which leads to smaller gas volumes and therefore smaller equipment with comparable production capacities.This results in a considerably higher conversion rate, if the residual gas is passed through the following converter beds (usually one or two). The SO3 which is formed in the second catalysis stage is absorbed in the final absorber.In general the process uses gases with an SO2 content of 10 t o11 %. The inlet gas temperature is about 4000C. Gases with lower temperatures require reheating from 50 to 4000C. This is usually carried out with recovered heats from the conversion process.operating(a) the double contact process at an elevated pressure of 5 bar increases the conversion rate by shifting the conversion equilibrium and favouring the formation of SO3.The disadvantages are higher electricity consumpt ion and, at the same time, less steam production. Higher NOx emissions are caused by higher sulfur combustion temperatures (18000C), but savings of 10 -17 % on investment costs are gained.Figure 3.2.2.1 Typical process flow sheet for a sulfur burning double catalysisplant.3.2.3 Wet catalysis processThe wet catalysis process is applicable to wet SO2 gases. The potential for the formation of sulfuric acid mist might require tail gas treatment.Wet SO2 gases (eg. from the burning of H2S gases or from the catalytic conversion of H2S gases) are directly supplied into the contact tower without previous drying. SO3 formed by the catalytic conversion immediately reacts with the moisture of the gases, thereby forming the acetic acid. The sulfuric acid is condensed in a condenser installed after the contact tower.FactorsSulfuric Acid Production By Lead Chamber processSulfuric Acid Production By single contact/single absorption processSulfuric Acid Production By double contact/double absorptio n processSulfuric Acid Production By Wet contact action processHealth and safety hazards involved little safe, waste gases are carry out to the atmosphereLess amount of SO3 is absorbed so the rest is discharged to the atmosphereA larger amount of SO3 is absorbedA larger amount of SO3 is absorbedOperating costHigh operating costLess operatingThe least operating costLess operating costRaw materialSO2, NO, NO2, O2, H2O.Melted sulfur, O2, SO2, SO3.Melted sulfur, H2O, O2, SO2, SO3.Wet SO2 gases, H2S, O2, SO3.Waste products and by products rake gases are discharged to the atmosphereLarge amounts of SO2 gas are discharged to the atmosphereLess amounts of SO2 gas are discharged to the atmosphere, less heat released after each successive catalyst bed.A larger amount of SO3 is absorbedEquipmentAcid Tower (Glover Tower), Lead Chambers, Reactor (Gay-lussac Tower)Air dryer, burner, waste heat boiler, converter, single absorption column.Air dryer, burner, waste heat boiler, converter, intermedi ate and external absorption column.Burner, convertor, acid tower.YieldYields 78% H2SO4New plants achieve 98 to99 % conversion ratesYields about 98%Yields 70 to 80 % H2SO4Environmental pollutionMore gases are discharged to the atmosphereMore gases discharged to the atmosphereLess gases discharged to the atmosphereMore gases are discharger to the atmospherePurity of productsLow purityLow purityHigh purityLow purityTable (3.2.1) Process selectionFactorsSulfuric Acid Production By Lead Chamber processSulfuric Acid Production By single contact/single absorption processSulfuric Acid Production By double contact/double absorption processSulfuric Acid Production By Wet Catalysis processHealth and safety hazards involved5553Operating cost6475Raw material6575Waste products and by products6675Equipment7586Yield5679Environmental pollution5564Purity of products6579Total (80)46415446Table (3.2.2) Process SelectionAccording to the discussion and the data presented above we choose the Double Contac t/Double Absorption process.CHAPTER FOURPROCESS DISCRIPTION4.1 Production of H2SO4 by double contact processThe process begins in the burner, in which the melt sulfur is pumped to the burner where it is burnt in an excess of dry air. The gas exiting the burner is maintained at (8 9%v/v) sulfur dioxide and approximately 830C due to the heat produced by the exothermic reaction.Sulfurs on burning gives about one third of heat combustion of coal ,and this heat raises the temperature of combustion gases more or less in accordance with the figure (4.1.1) as shown.Figure (4.1.1) Theoretical Flame Temperature.8This heat is high in temperature and there is plenty of it, consequently it is worth utilizing and the hot gases are led crosswise pipes through which the water passes. The water is heated, steam is raised and the gases are cooled.The sulfur dioxide/air gas mixture is then passed through the stream to converter. The sulfur dioxide is converted to sulfur trioxide by reacting with oxy gen over a catalyst.This reaction is described by the equation2SO2 + O2 2SO3 H = -100 kJ mol-1This reaction occurs in the converter, a four-stage reaction vessel with each stage consisting of a solid catalyst bed through which the gas is passed. The catalyst used is vanadium pentoxide (V2O5), and potassium sulphate dispersed on a silica base which forms a porous support, giving a large surface area for reaction.This reaction is exothermic and its equilibrium constant decreases with increasing temperature (Le Chatelier.s Principle).Figure (4.1.2) shows the percentage conversion of SO2 to SO3 that would be reached at an SO2 concentration of 8% v/v and a range of gas temperatures.However, the reaction rate is also temperature dependent, so that if the temperature becomes too low the equilibrium point will not be reached.In practice, the gas temperature must be maintained between (400 500C) to maintain a high reaction rate and also high conversion equilibrium.As the reaction is exother mic, heat is generated across each of the catalyst beds. This heat must be removed between each stage to maintain the optimum reaction temperature into the following stage. The temperature rise through each catalyst bed and the inter-stage cooling is shown in Figure (4.1.2).Figure (4.1.2) The Temperature Rise Through Beds.7The gas after passing through three catalyst bed goes to the first absorption tower where the Sulfur trioxide is removed. The gas is then reheated to about 420 C, passed through the fourth catalyst bed, then cooled and sent to a second absorption tower.The gas mixture goes to the first and second absorption tower, a packed tower where SO3 is absorbed into a counter-current flow of 98 99% sulfuric acid.The overall reaction can be described by the following equation, where sulfur trioxide reacts with the free water to produce sulfuric acidSO3 + H2O H2SO4 H = -200 kJ mol-1The circulating sulfuric acid must be maintained at about 98% concentration and temperature is controlled in the desired rang of (70C_90C) to maximize the absorption efficiency.The acid strength is important because the vapor pressure of sulfur trioxide above sulfuric acid is at a minimum at an acid strength of 98% (see Figure (4.1. 3)).At higher concentrations the increased vapor pressure is caused by SO3 and at lower concentrations the water vapor pressure increases sharply and the resultant acid mist is not readily re-absorbed and escapes to the atmosphere. A stream of sulfuric acid is continuously bled off and cooled through a plate heat exchanger before being passed into the storage tanks.Figure (4.1.3) Relation Between Vapor Pressure and Concentration.7Figure (4.1.4) Flow SheetCHAPTER FIVEENERGY AND majority BALANCE5.1 MASS BALANCE*DrierComponents substance%H201.271.3O221.1223N269.475.7Temperature25Cpressure1 atmM1M2Components issue forth%H2SO439.498H2O0.82Temperature150Cpressure1 atmM3ComponentsAmount%O221.1223.3N269.476.7Temperature25Cpressure1 atmM4ComponentsAmount %H2SO439.4295H2O2.15Temperature150Cpressure1 atm*BurnerM3ComponentsAmount%O221.1223.3N269.476.7Temperature26Cpressure1 atmM5ComponentsAmount%S3.76100ComponentsAmount%SO228.1629O27.047N269.464Temperature830Cpressure1 atmM6*ConverterM6ComponentsAmount%SO228.1629O27.047N269.464Temperature400Cpressure1 atmM7ComponentsAmount%O22.112N269.4466SO28.458SO324.6424Temperature450pressure1 atmM8ComponentsAmount%SO226.7226O21.691.6N269.4466.4SO326.7226Temperature450pressure1 atmM9ComponentsAmount%SO20.3146O20.07681.5N23.4766.5SO31.3626Temperature450pressure1 atmM10ComponentsAmount%SO20.3146O20.07681.5N23.4766.5SO31.3626Temperature450pressure1 atmM11ComponentsAmount%SO26.086O21.546N265.9766.5SO325.8426Temperature