Page 167 - Biofuels Refining and Performance
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150   Chapter Five


           ignition quality, cold flow, oxidative stability, viscosity, and lubricity.
           This chapter discusses the influence of the structure of fatty esters on
           these properties. Not all of these properties have been included in
           biodiesel standards, although all of them are essential to proper func-
           tioning of the fuel in a diesel engine.
             Generally, as the least expensive alcohol, methanol has been used to
           produce biodiesel. Biodiesel, in most cases, can therefore be termed the
           fatty acid methyl esters (FAME) of a vegetable oil or animal fat.
           However, as mentioned above, both the fatty acid chain and the alcohol
           functionality contribute to the overall properties of a fatty ester. It is
           worthwhile to consider the properties imparted by other alcohols yield-
           ing fatty acid alkyl esters (FAAE) that could be used for producing
           biodiesel. Therefore, both structural moieties will be discussed in this
           chapter. Table 5.1 lists fuel properties of neat alkyl esters of fatty acids.
           Besides the fuel properties discussed here, the heat of combustion (HG)
           of some fatty compounds [3] is included in Table 5. 1, for the sake of under-
           scoring the suitability of fatty esters as fuel with regard to this property.

           TABLE 5.1 Properties of Fatty Acids and Esters a
            Trivial (systematic)   MP c  BP c,d                      HG , f
             name; acronym b    ( C)    ( C)  Cetane no.  Viscosity e  (kcal/mol)
           Caprylic          16.5     239.3
            (Octanoic); 8:0
                                                           j
           Methyl ester               193     33.6 (98.6) g  0.99 ; 1.19 k  1313
           Ethyl ester        43.1    208.5             1.37 (25 ) j  1465
           Capric            31.5     270     47.6 (98.0) g       1453.07 (25 )
            (Decanoic); 10:0
                                                           j
           Methyl ester               224     47.2 (98.1) g  1.40 ; 1.72 k  1625
           Ethyl ester        20      243–5   51.2 (99.4) g  1.99 (25 )  j  1780
           Lauric            44       131 1                       1763.25 (25 )
            (Dodecanoic); 12:0
                                                           j
           Methyl ester      5        266 766  61.4 (99.1) g  1.95 ; 2.43 k  1940
           Ethyl ester        1.8fr   163 25            2.88 j    2098
           Myristic          58       250.5 100                   2073.91 (25 )
            (Tetradecanoic); 14:0
           Methyl ester      18.5     295 751  66.2 (96.5) g  2.69 j  2254
           Ethyl ester       12.3     295     66.9 (99.3) g       2406
           Palmitic          63       350                         2384.76 (25 )
            (Hexadecanoic); 16:0
                                                           j
                                                      g
           Methyl ester      30.5     415–8 747  74.5 (93.6) ; 3.60 ; 4.38 k  2550
                                               85.9 i
           Ethyl ester       19.3/24  191 10  93.1 i              2717
           Propyl ester      20.4     190 12  85.0 i
           Isopropyl ester   13–4     160 2   82.6 i
           Butyl ester       16.9             91.9 i
           2-Butyl ester                      84.8 i
           Isobutyl ester    22.5, 28.9 199 5  83.6 i
           Stearic           71       360 d   61.7 h              2696.12 (25 )
            (Octadecanoic); 18:0
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