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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
Photocatalytic removal of nitrate in wastewater has attracted wide attention because of its simple operation and environmental protection. However, the preparation of photocatalysts with high efficiency and high nitrogen selectivity is still a challenge. In this paper, TiO is grown in situ on TiC MXene by a simple calcination method and modified with silver particles. The presence of TiC reduces the recombination rate of photogenerated electrons and generates more photogenerated electrons. At the same time, the silver particles also increase the photoelectron density and further improve the carrier separation of the catalyst. Due to its unique structure and optical properties, the prepared photocatalyst shows an excellent nitrate removal rate under a high-pressure mercury lamp. At 500 mg/L, the nitrate removal rate reaches 96.1%, and the nitrogen selectivity reaches 92.6%. Even after 5 cycles, the prepared photocatalyst still maintains a high nitrate photocatalytic removal efficiency (89%). The electron transfer path is verified by density functional theory calculations.
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Source |
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http://dx.doi.org/10.1007/s11356-022-19616-x | DOI Listing |
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