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The reactive red 3 was degraded by catalytic wet oxidation process over Fe-RH-MCM-41 prepared by Direct Hydrothermal Technique (DHT) at Si/Fe molar ratio of 10 using silica from rice husk. The extended reaction conditions were studied as a function of reaction temperatures, initial H2O2 concentrations and initial pH of solutions designed by Box-Behnken design (BBD) based on Response Surface Methodology (RSM) to achieve the optimal condition and interaction of independent variables. The characterizations of catalyst were studied by XRD, BET surface area and TEM to explain the morphology of surface and to confirm the hexagonal structure. The results showed the 2theta peak can be indexed to hexagonal lattice that also confirmed by TEM result and surface area about 650 m2/g. All of independent variables showed significant on the degradation of reactive red 3 except for initial H2O2 concentration.

-RH-MCM-41 was synthesized by using silica from rice husk and further modified to increase acidity by adding Al with grafting method with Si/Al ratio of 75 and 25. The resulting materials were referred to as RH-AlMCM-41(75) and RH-AlMCM-41(25). The XRD spectra of all RH-AlMCM-41 confirmed a mesoporous structure of MCM-41. Surface areas of all RH-AlMCM-41 were in the range of 700-800 m 2 /g, lower than that of the parent RH-MCM-41, which was 1230 m 2 /g. After Al addition the Si/Al ratios of RHAlMCM-41(75) and RH-AlMCM-41(25) were higher than that of the parent RH-MCM-41. The RH-AlMCM-41 materials were used as supports for bimetallic platinum−iron catalysts, denoted as Pt-Fe/RH-AlMCM-41, with Pt and Fe amounts of 0.5 and 5.0% by weight, respectively. Results from TPR indicated that the presence of Al might assist the interaction between Pt and Fe as the reduction temperature of iron oxides shifted to a lower value. All catalysts were active for phenol hydroxylation using H 2 O 2 as an oxidant, for which the highest conversions were observed on the RH-MCM-41 material with the highest surface area. The acidity of the supports did not present a significant role in improving the catalytic performance.