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World Journal of Environmental Engineering

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Figure

Figure 1. Absorption of DCF at 290 nm and the reaction product (after electrolysis) at 450 nm (insert)
Figure 2. Three consecutive cyclic voltammograms of 100 µmol/L diclofenac in (NH4)2HPO4
Figure 6 shows the results at different temperatures (300°C, 400°C and 500°C). The GC-MS spectrum is quite different from those spectra shown above: No chlorinated products are detectable
Figure 5. GC-MS of DCF after treatment with H2O2: Peak 4.9: monochloroaniline; peak 5.1: dichlorophenol; peak 5.6: dichloroaniline; peaks around 9: dichlororbenzene derivatives; peaks around 11: dichlorophenyl-benzene; peak 13.5: decarboxylated DCF

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