Large Volume Inorganic Chemicals - Ammonia ... - ammk-rks.net
Large Volume Inorganic Chemicals - Ammonia ... - ammk-rks.net Large Volume Inorganic Chemicals - Ammonia ... - ammk-rks.net
Chapter 3Option 1 Option 2 Option 3Design values, lowsteam exportLow HNO 3concentration, lowsteam exportMost economicoption, high steamexportAbsorption pressure in bar 15 15 12Produced HNO 3 concentration in % 65 56 60NO x tail gas levelppm 100 40 130 – 170mg/Nm 3 205 82 267 – 349Table 3.11: Theoretical study of the optimisation of the absorption stage design at ZAK, Tarnow[88, infoMil, 1999]The nitric acid plant of Yara, Porsgrunn was built in 1992 and has a capacity of 2000 tonneHNO 3 /day. It is a M/H plant (5/11 bar). Due to the design of the absorption column and thetemperature of the cooling water (as a result of the climate in Porsgrunn, the temperature of thewater is 4 – 6 o C without cooling), NO x emissions at 80 – 90 ppm (164 – 185 mg/Nm 3 ) wereachieved without using an additional abatement system.The nitric acid plant of Agropolychim, Devnia was built in 2003, has a capacity of 1100tonnes/day and is designed as a M/H plant (3.5/12.8 bar). At absorption temperatures of 20 –40 ºC, NO x levels of 170 – 200 ppm are achieved.Economics• monopressure operation has been shown in the past to give special economical advantages.Capital costs are lower, because only one compression unit is required. When feedstock andenergy prices are low: low investment costs ensure a quick payback. If feedstock and energyprices are high, yield and energy efficiency must be maximised, so higher investment costsare more acceptable. Plant size also plays an important role. For a large production capacity(>1000 tonnes 100 % HNO 3 /day) it is more realistic to build a dual pressure plant• in a dual pressure system, stainless steel compressor units are necessary to compress NO X .As a result, dual pressure plants need investments that are approximately 15 – 20 % higherthan the investment for a monopressure plant. On the other hand, a dual pressure plantoptimises the NO yield and energy recovery, thereby recovering the higher investmentcosts. As stated above, a dual pressure plant is more feasible if a large production capacityis desired (>1000 tonne 100 % HNO 3 /day)• total costs for NO x removal using the HEA system were in 1998 USD 0.6/tonne HNO 3produced (about EUR 0.55/tonne HNO 3 produced, figures based on a 365 tonne 100 %HNO 3 /day plant).Driving force for implementationOptimised HNO 3 yield and lower NO x emissions.Reference literature and example plants[88, infoMil, 1999, 94, Austrian UBA, 2001], ZAK, Tarnow; Yara, Porsgrunn, Agropolychim,Devnia, Haifa Chemicals Ltd.120 Large Volume Inorganic Chemicals – Ammonia, Acids and Fertilisers
Chapter 33.4.5 N 2 O decomposition by extension of the reactor chamberDescriptionYara has developed and patented a technology that reduces the production of N 2 O by increasingthe residence time in the reactor at high temperatures (850 – 950 °C). This technology consistsof an ‘empty’ reaction chamber of approximately 3.5 m extra in length between the platinumcatalyst and the first heat exchanger. For illustration, see Figure 3.7. Due to the longer residencetime of 1 – 3 seconds, a N 2 O reduction of 70 – 85 % might be obtained, since N 2 O is metastableat higher temperatures and decomposes to N 2 and O 2 .NH 3airPlatinum gauze packExtended reactor chamberHeatrecoveryTo absorberFigure 3.7: Decomposition of N 2 O by extension of the reactor chamberFigure based on [87, infoMil, 2001]Achieved environmental benefitsThe example plant achieves an N 2 O emission level of 2 – 3 kg/tonne 100 % HNO 3 [80, Jenssen,2004, 104, Schöffel, 2001] or about 400 ppm [17, 2nd TWG meeting, 2004].Cross-media effectsNone believed likely.Large Volume Inorganic Chemicals – Ammonia, Acids and Fertilisers 121
- Page 98 and 99: Chapter 22.4.7 Advanced process con
- Page 100 and 101: Chapter 22.4.9 Combined Claus unit
- Page 102 and 103: Chapter 2Operational dataSee Descri
- Page 104 and 105: Chapter 22.4.12 Preheating of combu
- Page 106 and 107: Chapter 22.4.14 Isothermal shift co
- Page 108 and 109: Chapter 22.4.16 Stripping and recyc
- Page 110 and 111: Chapter 22.4.18 Use of sulphur resi
- Page 112 and 113: Chapter 22.4.20 Indirect cooling of
- Page 114 and 115: Chapter 22.4.22 Ammonia removal fro
- Page 116 and 117: Chapter 22.4.24 Metal recovery and
- Page 118 and 119: Chapter 2Driving force for implemen
- Page 120 and 121: Chapter 22.5 BAT for ammoniaBAT is
- Page 123 and 124: Chapter 33 NITRIC ACID3.1 General i
- Page 125 and 126: Chapter 3Pressure in bar Temperatur
- Page 127 and 128: Chapter 33.2.5 Tail gas properties
- Page 129 and 130: Chapter 33.3 Current emission and c
- Page 131 and 132: Chapter 3N 2 O emission levelProces
- Page 133 and 134: Chapter 3N 2 O emission levelProces
- Page 135 and 136: Chapter 3Process typeNO x emission
- Page 137 and 138: Chapter 3Process typeNO x emission
- Page 139 and 140: Chapter 3140120Generation factor %1
- Page 141 and 142: Chapter 33.4.2 Optimisation of the
- Page 143 and 144: Chapter 33.4.3 Alternative oxidatio
- Page 145 and 146: Chapter 33.4.4 Optimisation of the
- Page 147: Chapter 3Achieved environmental ben
- Page 151 and 152: Chapter 33.4.6 Catalytic N 2 O deco
- Page 153 and 154: Chapter 3According to [89, Kuiper,
- Page 155 and 156: Chapter 33.4.7 Combined NO x and N
- Page 157 and 158: Chapter 3EconomicsInvestment costs.
- Page 159 and 160: Chapter 3Operational dataSee descri
- Page 161 and 162: Chapter 3NOx removal efficiency in
- Page 163 and 164: Chapter 33.4.10 Addition of H 2 O 2
- Page 165 and 166: Chapter 33.4.11 NO X reduction duri
- Page 167 and 168: Chapter 3Installing a low temperatu
- Page 169 and 170: Chapter 3NO x emission level as NO
- Page 171: Chapter 3Operational dataNo specifi
- Page 174 and 175: Chapter 4Country Company Location C
- Page 176 and 177: Chapter 4Country Company Location C
- Page 178 and 179: Chapter 4Figure 4.2 gives an overvi
- Page 180 and 181: Chapter 4Two general converter type
- Page 182 and 183: Chapter 4Figure 4.6 gives an impres
- Page 184 and 185: Chapter 44.2.3 Sulphur sources and
- Page 186 and 187: Chapter 44.2.3.5 Non-ferrous metal
- Page 188 and 189: Chapter 4Sulphur source/SO 2 produc
- Page 190 and 191: Chapter 44.3 Current emission and c
- Page 192 and 193: Chapter 410Tail gas specific SO2 lo
- Page 194 and 195: Chapter 4Capacity in tonnesof 100 %
- Page 196 and 197: Chapter 4Capacity in tonnesof 100 %
Chapter 3Option 1 Option 2 Option 3Design values, lowsteam exportLow HNO 3concentration, lowsteam exportMost economicoption, high steamexportAbsorption pressure in bar 15 15 12Produced HNO 3 concentration in % 65 56 60NO x tail gas levelppm 100 40 130 – 170mg/Nm 3 205 82 267 – 349Table 3.11: Theoretical study of the optimisation of the absorption stage design at ZAK, Tarnow[88, infoMil, 1999]The nitric acid plant of Yara, Porsgrunn was built in 1992 and has a capacity of 2000 tonneHNO 3 /day. It is a M/H plant (5/11 bar). Due to the design of the absorption column and thetemperature of the cooling water (as a result of the climate in Porsgrunn, the temperature of thewater is 4 – 6 o C without cooling), NO x emissions at 80 – 90 ppm (164 – 185 mg/Nm 3 ) wereachieved without using an additional abatement system.The nitric acid plant of Agropolychim, Devnia was built in 2003, has a capacity of 1100tonnes/day and is designed as a M/H plant (3.5/12.8 bar). At absorption temperatures of 20 –40 ºC, NO x levels of 170 – 200 ppm are achieved.Economics• monopressure operation has been shown in the past to give special economical advantages.Capital costs are lower, because only one compression unit is required. When feedstock andenergy prices are low: low investment costs ensure a quick payback. If feedstock and energyprices are high, yield and energy efficiency must be maximised, so higher investment costsare more acceptable. Plant size also plays an important role. For a large production capacity(>1000 tonnes 100 % HNO 3 /day) it is more realistic to build a dual pressure plant• in a dual pressure system, stainless steel compressor units are necessary to compress NO X .As a result, dual pressure plants need investments that are approximately 15 – 20 % higherthan the investment for a monopressure plant. On the other hand, a dual pressure plantoptimises the NO yield and energy recovery, thereby recovering the higher investmentcosts. As stated above, a dual pressure plant is more feasible if a large production capacityis desired (>1000 tonne 100 % HNO 3 /day)• total costs for NO x removal using the HEA system were in 1998 USD 0.6/tonne HNO 3produced (about EUR 0.55/tonne HNO 3 produced, figures based on a 365 tonne 100 %HNO 3 /day plant).Driving force for implementationOptimised HNO 3 yield and lower NO x emissions.Reference literature and example plants[88, infoMil, 1999, 94, Austrian UBA, 2001], ZAK, Tarnow; Yara, Porsgrunn, Agropolychim,Devnia, Haifa <strong>Chemicals</strong> Ltd.120 <strong>Large</strong> <strong>Volume</strong> <strong>Inorganic</strong> <strong>Chemicals</strong> – <strong>Ammonia</strong>, Acids and Fertilisers