کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
9451345 1307812 2005 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
An assessment of the suitable operating conditions for the CeO2/γ-Al2O3 catalyzed wet air oxidation of phenol
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست شیمی زیست محیطی
پیش نمایش صفحه اول مقاله
An assessment of the suitable operating conditions for the CeO2/γ-Al2O3 catalyzed wet air oxidation of phenol
چکیده انگلیسی
It has been shown that the CeO2/γ-Al2O3 catalyst is a feasible alternative to CeO2 for the catalytic wet air oxidation (CWAO) of phenol because it remains an effective catalyst and yet is cheaper to prepare. In this study, we found that the optimal cerium content in the CeO2/γ-Al2O3 catalyst was 20 wt.%, regardless of catalyst loading. Furthermore, at 180 °C, with a phenol concentration of 1000 mg l−1, and an O2 partial pressure of 1.0 MPa or 1.5 MPa, the optimal catalyst loading was 3.0 g l−1. The efficacy of CWAO of phenol improved with O2 partial pressure, although the effects of O2 pressure were more significant between 0.5 MPa and 1.5 MPa than between 1.5 MPa and 2.0 MPa. After 2 h of reaction, approximately 100% phenol conversion and 80% total organic carbon (TOC) removal was recorded at 180 °C, 1000 mg l−1 of phenol and 3.0 g l−1 of catalyst. Because these percentages subsequently leveled off, it is suggested that 2 h is a suitable time over which to run the reaction. The efficacy of CWAO of phenol decreased as initial phenol concentration was raised (from 400 to 2500 mg l−1), with the exception of phenol conversion after about 2 h, for which 400 mg l−1 produced the lowest phenol conversion figure. Higher phenol concentrations require both catalyst loading and O2 partial pressure to be increased to maintain high performance. For example, for 2000 mg l−1 and 2500 mg l−1 phenol, nearly 100% phenol conversion and 90% TOC removal after 4 h of reaction at 180 °C required 4.0 g l−1 of catalyst and 2.0 MPa.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemosphere - Volume 58, Issue 4, January 2005, Pages 485-492
نویسندگان
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