Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process

博士 === 國立交通大學 === 環境工程所 === 91 === An evaluation of physicochemical characteristic of vanadia-titania catalyst for NO removal by selective catalytic reduction (SCR) process was conducted in this study. The intrinsic rate constant, effective rate constant and characteristic time were obtained using a...

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Main Authors: Chia-Hsin Lin, 林家欣
Other Authors: Hsunling Bai
Format: Others
Language:zh-TW
Published: 2003
Online Access:http://ndltd.ncl.edu.tw/handle/03834034858692834764
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spelling ndltd-TW-091NCTU05150342016-06-22T04:14:28Z http://ndltd.ncl.edu.tw/handle/03834034858692834764 Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process 釩鈦觸媒孔隙擴散限制及表面酸性之研究 Chia-Hsin Lin 林家欣 博士 國立交通大學 環境工程所 91 An evaluation of physicochemical characteristic of vanadia-titania catalyst for NO removal by selective catalytic reduction (SCR) process was conducted in this study. The intrinsic rate constant, effective rate constant and characteristic time were obtained using a mathematical model employing the effective factor method to describe physical and chemical characteristic of SCR reaction. The result showed that the physical enhancement was obvious by increasing pore radius that resulted in a higher effective diffusivity. One the contrast, decreasing pore radius that resulted in lower effective diffusivity and reduced the NO removal efficiency although it has higher surface area. The effects of operating parameters (moisture, vanadia content, working temperature) on the roles of Bronsted and Lewis acids acting in the SCR reaction were specified by the observed NO removals and the spectra of in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). The results indicated that H2O competed with NH3 molecules to be adsorbed on the pure titania catalyst that contained only Lewis acid sites. But competition did not occur over vanadia-based catalyst. Both Bronsted and Lewis acid sites appeared on vanadia-based catalyst in the presence of H2O. But a lower catalytic activity was observed and this may be due to less reaction sites are available as compared to that under dry conditions where only Lewis acid sites were found. It is concluded that surface acid sites are varied according to different operation conditions. Lewis acidity was dominant under the condition of low vanadia content and in the absence of H2O molecules. It is also less irrelevant to temperature. In contrast, Bronsted acidity was dominant under the condition of high vanadia content and with the presence of H2O molecules. It is also highly affected by temperature. Hsunling Bai 白曛綾 2003 學位論文 ; thesis 127 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 博士 === 國立交通大學 === 環境工程所 === 91 === An evaluation of physicochemical characteristic of vanadia-titania catalyst for NO removal by selective catalytic reduction (SCR) process was conducted in this study. The intrinsic rate constant, effective rate constant and characteristic time were obtained using a mathematical model employing the effective factor method to describe physical and chemical characteristic of SCR reaction. The result showed that the physical enhancement was obvious by increasing pore radius that resulted in a higher effective diffusivity. One the contrast, decreasing pore radius that resulted in lower effective diffusivity and reduced the NO removal efficiency although it has higher surface area. The effects of operating parameters (moisture, vanadia content, working temperature) on the roles of Bronsted and Lewis acids acting in the SCR reaction were specified by the observed NO removals and the spectra of in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). The results indicated that H2O competed with NH3 molecules to be adsorbed on the pure titania catalyst that contained only Lewis acid sites. But competition did not occur over vanadia-based catalyst. Both Bronsted and Lewis acid sites appeared on vanadia-based catalyst in the presence of H2O. But a lower catalytic activity was observed and this may be due to less reaction sites are available as compared to that under dry conditions where only Lewis acid sites were found. It is concluded that surface acid sites are varied according to different operation conditions. Lewis acidity was dominant under the condition of low vanadia content and in the absence of H2O molecules. It is also less irrelevant to temperature. In contrast, Bronsted acidity was dominant under the condition of high vanadia content and with the presence of H2O molecules. It is also highly affected by temperature.
author2 Hsunling Bai
author_facet Hsunling Bai
Chia-Hsin Lin
林家欣
author Chia-Hsin Lin
林家欣
spellingShingle Chia-Hsin Lin
林家欣
Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process
author_sort Chia-Hsin Lin
title Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process
title_short Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process
title_full Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process
title_fullStr Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process
title_full_unstemmed Study of Intra-Pore Diffusion and Surface Acidity of Vanadia/Titania catalyst for the SCR process
title_sort study of intra-pore diffusion and surface acidity of vanadia/titania catalyst for the scr process
publishDate 2003
url http://ndltd.ncl.edu.tw/handle/03834034858692834764
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