Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Heterocyclic aromatic hydrocarbons are concerned pollutants with carcinogenic toxicity, which exist universally in various environmental matrices and have great harm to environmental and human health. In present work, magnetic resorcinol-formaldehyde composites (FeO@SiO@R-F) were fabricated via aldol condensation reaction under alkaline condition. The prepared magnetic materials were examined and analyzed with Fourier transform infrared spectroscopy and other related instruments. The FeO@SiO@R-F composites were utilized to develop an efficient magnetic solid phase extraction (MSPE) method for extracting six heteropolyclic aromatic hydrocarbons from environmental water samples including carbazole (CB), 7-methylquinoline (7-MQL), 9-methylcarbazole (9-MCB), dibenzothiophene (DBT), 4-methyldibenzothiophene (4-MDBT), and 4,6-dimethyldibenzothiophene (4,6-DMDBT). The analytes were analyzed by high performance liquid chromatography-ultraviolet variable wavelength detector (HPLC-VWD). The main factors affecting MSPE were optimized. With the optimal parameters, 9-MCB and 4-MDBT have good linearity over the concentration range of 0.1-300 μg L, and 7-MQL, CB, DBT and 4,6-DMDBT have good linearity over the concentration range of 0.5-300 μg L. The limits of detection were over the concentration range of 0.012-0.031 μg L. This method was successfully employed to measure real waters, and the spiked recoveries ranged from 89.4% to 99.9%. The results confirmed that the developed method was reliable, robust and could be employed as a usefully alternate way for analyzing such pollutants in waters.
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http://dx.doi.org/10.1016/j.talanta.2024.125864 | DOI Listing |