Advanced oxidation processes involving O3/H2O2 and O3/catalyst were used to compare the degradability and the effect of pH on the oxidation of 1,4-dioxane. Oxidation processes were carried out in a bubble column reactor under different pH. Initial hydrogen peroxide concentration was 3.52 mM in O3/H2O2 process and 115 g/L (0.65 wt.%) of activated carbon impregnated with palladium was packed in O3/catalyst column. 1,4-dioxane concentration was reduced steadily with reaction time in O3/H2O2 oxidation process, however, in case of O3/catalyst process, about 50～75% of 1,4-dioxane was degraded only in 5 minutes after reaction. Overall reaction efficiency of O3/catalyst was also higher than that of O3/H2O2 process. TOC and CODCr were analyzed in order to examine the oxidation characteristics with O3/H2O2 and O3/catalyst process. The results of CODCr removal efficiency and ΔTOC/ΔThOC ratio in O3/catalyst process gave that this process could more proceed the oxidation reaction than O3/H2O2 oxidation process. Therefore, it was considered that O3/catalyst advanced oxidation process could be used as a effective oxidation process for removing non-degradable toxic organic materials.

The mechanism of stomatal closing in response to O_3 was indirectly investigated by using H_2O_2 which is the intermediate product of O_3 metabolites. Stomata in epidermal strips close in response to H_2O_2. The effect of H_2O_2 on stomatal closing was dependent on the concentration of H_2O_2. 10 ppm H_2O_2 showed a clear effect on stomatal closing and 1000 ppm H_2O_2 induced complete stomatal closing after the treatment of 3 hours. Stomatal closing by H_2O_2 in intact leaf was also observed by measuring the diffusion resistance with porometer. It was found that the stomatal closing by H_2O_2 was not mediated by Ca^2+, and that was a different result observed in stomatal closing by water stress. Reversely, Ca^2+, showed a great inhibition on stomatal closing. The leakage of K^+ in epidermal strips was doubled in response to H_2O_2 when it was campared to the control. 10 ppm H_2O_2 decreased photosynthetic activity. Fv/Fm representing the activity of Photosystem Ⅱ was reduced about 4 % in 10 ppm H_20_2 and 8 % in 100 ppm H_2O_2 in the treatment of 1.5 hour. However, stomatal closing by 10 ppm H_2O_2 was reduced about 56 %. Accordingly, it can be suggetsted that stomatal closing by H_2O_2 is related with the decrease of photosynthetic activity, but it was chiefly induced by the change of the membrane permeability.