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
Bisphenol A (BPA) is a typical kind of endocrine disruption chemical, which has a negative effect on human health, and thus it is necessary to remove BPA from water. Herein, activation of peroxymonosulfate (PMS) by Fe, Cu-Coordinated ZIF-Derived Carbon Framework bifunctional catalyst (Fe/Cu@NC-x) fabricated via hydrothermal-calcination method for BPA removal. The physicochemical properties of Fe/Cu@NC-x were studied by X-ray diffraction, Transmission electron microscopy, Scanning electron microscopy, Raman Spectroscopy, Brunauer-Emmett Teller, and X-ray photoelectron spectroscopy. The effects of the Fe/Cu@NC-900 dosage and PMS concentration, initial pH, and co-existing anions on BPA degradation were evaluated. Under optimized factors (pH unadjusted, Fe/Cu@NC-900 = 0.2 g/L, and PMS = 0.75 g/L), the degradation efficiency of BPA can reach 98% after 30 min. In addition, the BPA degradation efficiency was different extents restrain by inorganic anions (SO > Cl > HCO > NO). Furthermore, the free radicals (SO·, ·OH, and O·) and non-radical (O) contribute to rapid BPA degradation in Fe/Cu@NC-900/PMS system. This study presents a novel material with significant performance for the removal of organic pollutants.
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Source |
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http://dx.doi.org/10.1016/j.chemosphere.2021.133455 | DOI Listing |
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