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
Although sulfite-based advanced oxidation processes (AOPs) have received renewed attention due to the production of oxysulfur radicals, the feasibility of using ultrasound (US) to activate sulfite remains unknown. In this work, low frequency ultrasound has been applied for the first time to develop a novel sulfite activation process (US-S(IV)) for enhanced oxidation of arsenite (As(III)). Our results showed that the US-S(IV) process with 1 mM sulfite addition and 20 kHz 650 W ultrasound can achieve approximately 2.9-fold increase in As(III) oxidation rate compared to the US process at pH 7. The mechanisms underpinning the US-S(IV) process have been probed through radical-scavenging experiments and electron spin resonance (ESR) spectrometry. Direct ultrasonolysis of sulfite has been demonstrated to be the predominant pathway producing the primary sulfite radical (SO⁻) in the US-S(IV) process. Besides, the US-S(IV) process also works well in the treatment process of natural water, suggesting that this process could be promising in commercial scale application. This work not only provides a new application of ultrasound in sulfite-based AOP, but also provides further insights into how sulfite impacts the US process.
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Source |
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http://dx.doi.org/10.1016/j.chemosphere.2021.130860 | DOI Listing |
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