{"title":"Effect of Silica on Nitrate-Incorporated Vanadia Catalysts in Low-Temperature Selective Catalytic Reduction of Nitrogen Oxides","authors":"Gibum Kwon, Shin Ae Song, Duck Hyun Lee","doi":"10.1021/acsomega.6c06102","DOIUrl":null,"url":null,"abstract":"<p>Developing shaped\r\ncatalysts for the low-temperature selective catalytic\r\nreduction (SCR) of NO<sub><em>x</em></sub> often results in\r\nsevere physical detachment and efficiency loss. Building on our previous\r\ndevelopment of highly active nitrate-incorporated V<sub>2</sub>O<sub>5</sub>–WO<sub>3</sub>/TiO<sub>2</sub> powder catalysts, we\r\ninvestigated the effect of SiO<sub>2</sub> as a structural binder\r\nfor coating these catalysts onto glass fiber sheets. Coatings with\r\n0–30 wt % SiO<sub>2</sub> were prepared and evaluated. The\r\naddition of 10 wt % SiO<sub>2</sub> significantly improved catalyst\r\ndispersion, coating uniformity, and mechanical adhesion, successfully\r\npreventing the structural degradation typically observed under highly\r\nhumid operating conditions. Consequently, the SiO<sub>2</sub>-containing\r\ncatalyst demonstrated enhanced physical stability, maintaining consistent\r\nNO<sub><em>x</em></sub> removal efficiencies for at least\r\n80 h, whereas the SiO<sub>2</sub>-free coating showed progressive\r\ndeactivation due to physical peeling. The optimized catalyst (10 wt\r\n% SiO<sub>2</sub>, 4 wt % V<sub>2</sub>O<sub>5</sub>) achieved a 98.7%\r\nNO<sub><em>x</em></sub> removal efficiency at 180 °C\r\nunder dry conditions and 95.2% in the presence of 10 vol % H<sub>2</sub>O. These findings clearly demonstrate that SiO<sub>2</sub> acts as\r\nan exceptionally robust structural binder, effectively bridging the\r\ngap between highly active fundamental powders and macroscopically\r\nstable industrial applications.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"11 41","pages":"63101–63109"},"PeriodicalIF":5.2000,"publicationDate":"2026-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Omega","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsomega.6c06102","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/29 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Developing shaped
catalysts for the low-temperature selective catalytic
reduction (SCR) of NOx often results in
severe physical detachment and efficiency loss. Building on our previous
development of highly active nitrate-incorporated V2O5–WO3/TiO2 powder catalysts, we
investigated the effect of SiO2 as a structural binder
for coating these catalysts onto glass fiber sheets. Coatings with
0–30 wt % SiO2 were prepared and evaluated. The
addition of 10 wt % SiO2 significantly improved catalyst
dispersion, coating uniformity, and mechanical adhesion, successfully
preventing the structural degradation typically observed under highly
humid operating conditions. Consequently, the SiO2-containing
catalyst demonstrated enhanced physical stability, maintaining consistent
NOx removal efficiencies for at least
80 h, whereas the SiO2-free coating showed progressive
deactivation due to physical peeling. The optimized catalyst (10 wt
% SiO2, 4 wt % V2O5) achieved a 98.7%
NOx removal efficiency at 180 °C
under dry conditions and 95.2% in the presence of 10 vol % H2O. These findings clearly demonstrate that SiO2 acts as
an exceptionally robust structural binder, effectively bridging the
gap between highly active fundamental powders and macroscopically
stable industrial applications.
ACS OmegaChemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍:
ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.