Page 253 - Chemistry ICSE Class X
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Study of Compounds–Nitric Acid                                                                       239
                                 >200°C
                     4HNO (l)  o         4NO (g)    +   O (g)   +   2H O(g)
                                                2
                                                            2
                           3
                                                                         2
                      nitric acid        nitrogen dioxide     oxygen
                     y the residue (K SO ) left in the retort would form a hard crust
                                   2
                                       4
                     which sticks to the glass. Its removal becomes a problem.
            ƒ  Conc. hydrochloric acid [HCl(aq)] should not be used in place of conc.
               sulphuric acid (H SO ). This is because HCl is volatile and therefore
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                                    4
               the HNO  vapour will also contain HCl vapour.
                        3
          How is nitric acid obtained on industrial scale
          On industrial (or commercial) scale, nitric acid can be obtained by Ostwald’s
          process described below.
          In this process, nitric acid is produced by the oxidation of ammonia.
              According to the Le-Chatelier’s principle, the favourable conditions
          for this reaction are,
            ƒ  Temperature. 750–900°C (800°C is the optimum value)
            ƒ  Pressure. 6–7 atm
            ƒ  Ammonia : Air ratio. 1 : 8 (by volume)
            ƒ  Catalyst. Pt (90%) + Rh (10%)
              About 90–95% yield is achieved in this reaction.


          Description of the plant
          The plant used in the process is shown in Fig. 10.2 and
          consists of the following parts:
            ƒ  Catalytic converter. %CVCN[VKE EQPXGTVGT KU ſVVGF YKVJ
               a platinum-rhodium gauze. The gauze is initially
               heated to 800°C electrically. As the oxidation of
               ammonia is an exothermic reaction, therefore, no
               external heating is required subsequently.
              A mixture of ammonia and clean air (volume ratio
          1 : 8) is passed through the gauze. Here, ammonia gets         Fig. 10.2  The Ostwald’s process for the manufacture
          oxidised to nitric oxide (NO).                                               of nitric acid
                                               Pt–Rh
                     4NH (g)     +   5O (g)   o      4NO(g)   +  6H O(g)
                          3
                                        2
                                                                       2
                                               800°C
            ƒ  Oxidation tower.  The nitric oxide containing nitrogen and some
               water vapour coming out of the converter are cooled to about 100°C
               by passing through coolers. In oxidation tower, nitric oxide is mixed
               with more air and it gets converted to NO .
                                                        2
                      2NO(g)     +   O (g)     o      2NO (g)
                                       2
                                                            2
                     nitric oxide      from air      nitrogen dioxide
            ƒ  Absorption tower. Nitrogen dioxide is allowed to enter the absorption
               tower from the lower end. Water is sprinkled from the top of the tower    ǀĞƌLJ ϭϬϬϬ Đŵ  ĂƌĞĂ ŽĨ ƚŚĞ ŐĂƵnjĞ
                                                                                                 2
               packed with quartz pieces. Here, NO  is absorbed into water in the      ƉƌŽĚƵĐĞƐ ĂďŽƵƚ ϱϬϬ ŬŐ ŽĨ ŶŝƚƌŝĐ ŽdžŝĚĞ
                                                    2
               presence of air to yield nitric acid.                                   ĞǀĞƌLJ Ϯϰ ŚŽƵƌƐ͘
                4NO (g) +  2H O(l) +  O (g)  o 4HNO (aq)
                                                            3
                    2
                                          2
                               2
                nitrogen dioxide          from air      nitric acid
          How to increase the concentration of nitric acid                              ŽŵŵĞƌĐŝĂů ŶŝƚƌŝĐ ĂĐŝĚ ŚĂƐ Ă ďƌŽǁŶ
          The aqueous nitric acid obtained by this method can be concentrated by       ĐŽůŽƵƌ ĚƵĞ ƚŽ ƚŚĞ ĚŝƐƐŽůǀĞĚ EK ͘
                                                                                                              2
                                                                                        ŽůŽƵƌůĞƐƐ ĂĐŝĚ ĐĂŶ ďĞ ŽďƚĂŝŶĞĚ
          distillation to ~ 68.5% (by mass). Further concentration to 98% acid (called   ĨƌŽŵ ƚŚĞ ďƌŽǁŶŝƐŚ ĂĐŝĚ ďLJ ďƵďďůŝŶŐ
          fuming nitric acid) can be achieved by  dehydration with concentrated        ĚƌLJ Ăŝƌ ƚŚƌŽƵŐŚ ǁĂƌŵ ĐŽŵŵĞƌĐŝĂů
          sulphuric acid.                                                              ŶŝƚƌŝĐ ĂĐŝĚ͘ dŚŝƐ ƉƌŽĐĞĚƵƌĞ ĚƌŝǀĞƐ
              Anhydrous nitric acid can be obtained by distillation of concentrated    ĂǁĂLJ ƚŚĞ ĚŝƐƐŽůǀĞĚ ŶŝƚƌŽŐĞŶ ĚŝŽdžŝĚĞ
          aqueous nitric acid with phosphorus pentoxide (P O  or P O ).                ĂŶĚ ƚŚĞ ĂĐŝĚ ďĞĐŽŵĞƐ ůŝŐŚƚ ŝŶ ĐŽůŽƵƌ͘
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