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    National Fertilizers Ltd.Bathinda

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    Sections

    Ammonia Plant

    Urea Plant

    Steam Generation Plant

    Bagging Plant

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    Ammonia Plant

    Desulphurization Section

    Reforming Section

    Shift Section

    Carbon Dioxide Removal Section

    Methanation Section

    Ammonia Synthesis Section

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    HYDROGENATOR: Reactions involved in Hydrogenator are:

    RSH + H 2 RH + H 2S

    R 1SSR 2 + 3H 2 R 1H + R 2H + 2H 2S

    R 1SR

    2 + 2H

    2 R

    1H + R

    2H + H

    2S

    COS + H 2 CO + H 2S If some content of CO 2 is also exist in Natural Gas feed then:

    CO + H CO + H O

    CO + H S COS + H O CoMo or NiMo based catalyst is used in Hydrogenator.

    Desulphurization Section

    Natural Gas Feed

    Recycle Hydrogen

    Feed Gas Preheater

    Hydrogenator

    Sulphur

    AbsorberNo. 1

    400 oC38 Kg/cm 2

    395 oC

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    Desulphurization Section

    H S ABSORBER: The Hydrogenated Natural Gas is fed to the Sulphur Absorbers.

    Zinc oxide catalyst is in the form of 4 mm cylindrical extrudates.

    Operating temperature is approx. 395C.

    ZnO + H S ZnS + H O

    ZnO + COS ZnS + CO

    Sulphur content in the natural gas is less than 0.1 ppm by weight.

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    Reforming Section

    Desulphurized gas is converted into synthesis gas by catalytic reforming of thehydrocarbon mixture with steam and the addition of air.

    Reactions involve in Reformer Section:

    CnH2n+2 + 2H O Cn-1H2n + CO + 3H - heat

    CH + 2H O CO + 4H - heat

    CO + H CO + H O heat

    Reactions take place in two steps

    1. Primary reforming

    2. Secondary reforming

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    Primary Reformer

    Desulphurized Gas

    Process Steam

    Preheater

    PrimaryReformer

    785-795 o

    520 oC

    34 - 31 kg/cm2 g

    Steam Carbon Mole Ratio=3/1

    Composition of catalyst (% w/w)1. Nickel Monoxide, NiO (17)2. Calcium Oxide, CaO (7)3. Potassium oxide, K2O (4)4. Aluminum Oxide , Al 2O 3 (Balance)

    Composition : (Mole%)(At Inlet of CatalystTubes)Ar 0.02CH4 79.68CO 2 ppm

    CO2 0.24H2 4.09N2 2.54C2H6 6.48C3H8 2.63C4H10 1.88C6H12 - 0.24

    As we have seen that we are getting around

    12.86 mole % of methane and we dont want

    it to be exist in stream just because it will be

    acting as inert in whole further processes.

    So we have to remove it.

    `For removing this access of methane we

    use Secondary Reformer.

    P r o

    d u c t

    S t r e a m

    o f P r i m a r y

    R e f o r m e r

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    Secondary Reformer

    The process gas is mixed with air with keeping theratio of H2/N2 Ratio: 3.0.

    Partial combustion takes place in the top of reactor. Methane concentration is 0.60 mole%. Outlet gas contains about 13.05mole% CO and

    7.24mole% CO that are removed further becausecatalyst may get poisioned.

    791 oC

    30 kg/cm2 g

    Catalystcomposition(%mole):

    NiO = 8 10%Al2O3 = 87 90 %Cao = < 0.05 %

    Gas inletcomposition (mole%)Ar 47 ppmCH4 12.86CO 9.5CO2 10.70

    H2 66.20 N2 0.74

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    CO Shift Section

    Exothermic reaction which occurs in this section is:

    CO + H 2O H2 + CO 2 + heat

    Shift reaction takes place in the two CO converters:

    1. HT CO-Converter.

    2. LT CO- converter with process gas cooling after each converter.

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    Methanator trimheater

    HT/LT CO Convertors

    Process gas from Reformer Section

    HT CO

    Convertor

    Waste heatboiler BFW Preheater 1 BFW

    360 oC29.6kg/cm 2

    432 oC205 oC

    205 oC28.6kg/cm 2

    227 oC

    LT COConvertor

    Catalysts composition(mole%) which isavailable in pellet form.Fe2O3 - 85- 95 %Cr 2O3 - 7-9 %CuO - 1-2%Al2O3 - 1.0%

    Catalyst cooxides of CAl, Which

    active in be250 oC.

    Composition (mole%)of inlet stream of HTCO Converter is:Ar 0.27, CH4 0.60,CO 13.37, CO2 7.65 , H2 55.61, N2 22.47

    Composition (mole%)of outlet stream of HTCO Converter is:Ar 0.24, CH4 0.55CO 3.22, CO2

    15.94H2 59.59, N2 20.48

    CoCAC1H

    340 oC

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    CO 2 Removal Section

    Outlet gas from CO converter contain 18.32 mole% CO2 Based on two stage activated MDEA process The solvent used for CO2 absorption is aMDEA(40%) Consists of a two stage CO2 absorber, a CO2 stripper and

    two flesh vessels.

    These are the reactions occurs in CO 2 removal section.R 3 N + CO2 + H 2O R 3 NH + + HCO 3-

    2R 2 NH + CO 2 R 2 NH 2+ + R 2 N-COO -

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    CO2 to Urea

    Condensate

    StripperReboiler

    HEL S Pump

    Cooler

    Chiller

    L PFlash

    HPPump

    BFW

    Preheater

    Semilean Sol n

    Lean Solution

    Stripper160C 27.8 Kg/cm2

    131C

    65

    50C 5.1 Kg/cm2

    72C 0.59 Kg/cm2

    95C

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    Methanation Section

    Methanation, a process in which the residual Carbon Oxides (CO, CO 2) are converted intoMETHANE because it acts as inert in Ammonia Synthesis Section.

    Reactions involve in Methanator are:

    CO + 3H 2 CH 4 + H 2O + heat

    CO2 + 4H 2 CH 4 + 2H 2O + heat

    As we can see these reactions are exothermic so Low temperature, high pressure and alow water vapour content favours the methanation equilibrium.

    After converting all Carbon Oxides into METHANE, product stream is pressurised from25Kg/cm 2 to 187Kg/cm 2 by using compressors and gas boosters and for maintainingtemperature, chillers are being used.

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    Gas/GasHE

    Trimheater

    Process gas fromHT CO Converter

    Process gas forLT CO Converter

    Synthesis Gas FroCO 2 Removal Se

    Methanator

    Synthesis gas to loop

    60C 26.8 Kg/cm2

    285 C

    300 C

    322 C

    90C 25 Kg/cm2

    Nickel based catalystis used here in methanatorwhich consist around 27%wt Nickel. (280-420 C)

    Composition(%at inlet is:

    Ar- 0.29, CH4- CO2-0.05,CO-0H2- 74.29,N2- 2

    Composition(%mole)at inlet is:

    Ar- 0.29, CH4- 1.08,H2- 73.95, N2- 24.88

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    High pressure and low temperature favourable equilibrium conditions of ammoniareaction.

    About 20% of N2 and H2 is converted into ammonia at given operating conditions. Unconverted remainder is recycled back.

    There are three beds we use in Ammonia Convertor:First bed : 370-510 C Second bed: 425-480 C Third bed: 420-460 C

    Ammonia Synthesis Section

    3H 2 + N 2 = 2NH 3 + heat ( H = 92.4 kJ/mol) 130C 187 Kg/cm

    Feed gas inlet

    Feed gas in

    Fe Oxied (Fe3O4) % wt 93 2 CaO, Al 2O 4, K2O, SiO 2, % wt 7 2With the irregular shape beadswith the size of 1.5-3mmBulk density 2.8kg/l

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    130C 187Kg/cm 2

    StartupHeater

    Product letDown tank

    AmmoniaSeparator

    Purg

    Makeup SynthesisGas

    Ammonia

    Converter

    Cooler

    SynthesisHotHeatExchanger

    SteamBoiler HE

    Chiller

    Compressors

    10C

    10C

    11

    27

    12

    25

    10C 178.9Kg/cm 2

    354C 270C 180C

    Composition(mole%) atOutlet of AmmoniaConverterAr- 2.11, CH4- 7.14 H2- 52.84, N2- 17.61

    NH3- 20.30

    ComPurConAr-H2

    NH

    CoDCoAH

    N

    ComStreAr-H2-

    NH

    Composition(mole%) atInlet of AmmoniaConverterAr- 1.82, CH4- 6.18 ,

    H2- 65.95, N2- 21.99, NH3- 4.06

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    Ammonia Recovery

    AmmoniaReflux

    AmmoniaOH Drum

    DistillationColumn

    Reboiler

    Purge GasAbsorber

    Lean Sol n Cooler

    Circulation Pump

    Purge Gas

    Let Down Gas

    Steam

    RichleanSol n

    Exchanger

    Fuel

    248C

    11C 27Kg/cm 2

    10C 178.9Kg/cm 2

    61C 20Kg/cm 2

    45C 25Kg/cmComposition(mole%) of

    Purge Gas:Ar- 2.49, CH4- 8.38

    H2- 82.48, N2- 20.82 NH3- 5.82

    Composition(mole%) ofLet Down Gas:Ar- 3.16, CH4- 16.12 H2- 38.06, N2- 15.76

    NH3- 26.88

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    Conclusion

    National Fertilizer Ltd. Bhatinda is producing 99.80% pure Ammoniaby Using Natural Gas with the help of helder tropsch method forfurther production of Urea.

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    Thank You !!!