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258    Cha pte r  Ei g h t


























            1.00              27.50    5.47  5.54  9.55  7.71  24.23  36.22  28.72  237.94  37.84


             7.0  6.5  6.0  5.5  5.0  4.5  4.0  3.5  3.0  2.5  2.0  1.5  1.0
                                        ppm
          FIGURE 8.1  NMR spectra of transesterifi ed Jatropha oil with methanol.


               detector. The used capillary is 30 m long with an internal diameter of
               0.25 mm. The carrier gas is nitrogen at a flow rate of 1 mL/min. The
               injection port temperature is 150°C and the ionization detector tem-
               perature is 170°C.
                   The transesterified product can also be analyzed by nuclear
               magnetic resonance (NMR). A reaction aliquot is taken with CDCl  in
                                                                      3
               a NMR tube and is placed in a NMR spectroscope (400 MHz, Bruker
               BioSpin, Fällanden, Switzerland) for analysis. The percentage conver-
                                                   1
               sion of reactant to product is analyzed by  H NMR (Fig. 8.1), consid-
               ering the peak of methoxy groups in the methyl esters at δ = 3.7 ppm
               (singlet) and of the  α-carbonyl methylene groups of fatty ester
               derivatives at δ = 2.3 ppm. The percentage of conversion is equal to
               (2 × A   /3 × A   ) × 100 where A is the integrated peak area at
                     δ = 3.7  δ = 2.3
               different chemical shifts.

               8.1.3  Property Measurement of Transesterified Oils
               The suitability of any material as fuel, including biodiesel, is influ-
               enced by the nature of its major components as well as that of minor
               components arising from production or other sources. The nature of
               these components ultimately determines the fuel and its physical
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