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244  4 Life Cycle Impact Assessment

          Table 4.10  ODP (based on mass) of some ozone-depleting gases according to WMO
          (1999); time horizon ∞ (stationary model).

          Compound                                     Residence time Life span  ODP
                                                             (a)       (a)  (kg CFC11
                                                           R        OH
                                                                            eq/kg)
          CFC-11, trichlorofluoromethane (CCl F)            45      <6400     1.0
                                   3
          CFC-12, dichlorodifluoromethane (CCl F )          100     <6400     0.82
                                    2 2
          CFC-113, trichlorofluoroethane (CCl FCClF )       90        —       0.90
                                  2    2
          CFC-114, 1,2 dichloro-1,1,2,2-tetrafluoroethane (CF ClCF Cl)  —  —  0.85
                                            2
                                                2
          CFC-115, chlorine-1,1,2,2,2-pentafluoroethane (CF ClCF )  —  —      0.40
                                           2    3
          Tetrachloromethane (CCl )                        35       >130     1.20
                           4
          Methyl chloride (CH Cl)                        About 1.3  1.3      0.02
                       3
          HCFC-22, chlorodifluoromethane (CHClF )          11.8      12.3    0.034
                                      2
          HCFC-123, 2,2-dichloro-1,1,1-trifluoroethane (CF CHClF)  —  —      0.012
                                           3
          HCFC-124, 2-chlorine-1,1,1,2-tetrafluoroethane (CF CHClF)  —  —    0.026
                                            3
          HCFC-141b, 1,1-dichloro-1-fluoroethane (CFCl CH )  9.2     10.4    0.086
                                         2
                                            3
          HCFC-142b, 1-chloro-1,1-difluoroethane (CF ClCH )  18.5    19.5    0.043
                                        2   3
          1,1,1-trichloroethane (CH CCl )                  4.8      5.7      0.11
                              3
                           3
          Halon 1301, bromine trifluoromethane (CBrF )      65        —       12
                                        3
          Halon 1211, bromine chlorodifluoromethane (CBrClF )  11     —       5.1
                                              2
          Halon 2402, 1,2-dibromo-1,1,2,2-tetrafluoroethane (CBrF CBrF )  —  —  6.0
                                                2   2
          Methyl bromide (CH Br)                           0.7      1.8   0.37 (0.2-0.5)
                        3
          Dinitrogenmonoxide (N O)                         120       —      0.017 c
                          2
          a Average tropospheric retention. 197)
          b
          Average tropospheric life span, computed from the OH-reaction constant and an average concentration of
          OH-radicals in the troposphere. 197)
          c
          Interim values according to Ravishankara, Daniel and Portmann (2009), see text above.
                    In this regard it should be noted, that about two-third of the total emission of N O
                                                                                  2
                                              −1
                    is natural and one-third (10.5 Mt a ) anthropogenic.
                      Lane and Lant 198)  recommend that these findings should be included into the
                    ozone depletion category of LCIA, if N O emissions are significant. They propose to
                                                 2
                    use the ODP calculated as interim characterisation factor for mid-point modelling.
                    As a result, land use, agriculture and industries contributing to N O emissions
                                                                         2
                    would also contribute to ozone depletion.
                      The release of N O into the troposphere is essentially due to bacterial metabolism
                                  2
                    in the soil. It is enforced by fertilisers containing nitrogen in agriculture whereby
                    the percentage of the nitrogen converted into N O is possibly underestimated. 199)  A
                                                         2
                    practical aspect for the proposed inclusion is that N O emissions have to be recorded
                                                           2
                    anyhow for calculating the GWP within the impact category ‘Climate change’.
                    197) Numerical values according to WMO (1999); for the definition of residence time and lifetime see
                        Kl¨ opffer and Wagner (2007a).
                    198) Lane and Lant (2012).
                    199) Crutzen et al. (2007).
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