Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
A Cu-Zn/core-shell Al-MCM-41 catalyst with various Cu and Zn species was investigated for selective catalytic reduction of NO with NH₃. The roles of Zn in the NO adsorption properties and the acidity of the catalysts were studied by temperature-programmed desorption of NO and Fourier transform infrared spectroscopy of NO+O₂ adsorption and NH₃ adsorption. The presence of Zn can promote the number of acid sites and improve the NO adsorption capacity by providing the additional sites for NO adsorption and subsequent nitrite and nitrate formation. Based on the experimental results, a possible reaction pathway was suggested. Cu-Zn/Al-MCM-41 exhibited higher activity compared with that of Cu/Al-MCM-41, having an average NO conversion of 73%. However, the average NO conversion was increased to 77% when Zn was loaded as ZnO form instead of various Zn species. X-ray adsorption near edge structure during reduction by H₂ revealed that there is a higher number of Cu in Cu-ZnO/Al-MCM-41 than that in Cu-Zn/Al-MCM-41. Under wet condition, the average NO conversion of Cu-ZnO/core-shell Al-MCM-41 was dropped to 68%. However, activity of Cu-ZnO/core-shell Al-MCM-41 was more stable than that of Cu-Zn/core-shell Al-MCM-41.
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Source |
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http://dx.doi.org/10.1166/jnn.2019.15756 | DOI Listing |
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