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 nanosheet structure of FeO/g-CN magnetic composite has been prepared and utilized as adsorbent for the ultrasound-assisted dispersive magnetic micro-solid-phase extraction of the ultra-trace inorganic mercury [Hg(II)]. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction and Fouries transform infrared spectroscopy images manifested that the hydrothermal systhesis promoted the binding of FeO particles with g-CN. The enrichment performance of composites depended on their compositions, and the recovery of Hg(II) on C-m30 (with FeO/g-CN mass ratio 2:3) was higher than that on other ratios. Recorded data showed that ultrasound wave was an effective method for reducing the agglomeration of magnetic materials and enhancing their adsorption properties. The Hg signal obtained by 80% power input is 3.2 times stronger than the signal by strring mode. X-ray diffraction characterization of the recovered adsorbent showed that g-CN needed to be updated after repeated use for four times. In addition, competitive adsorption may be main factor affecting the inhibitory effect of high concentration methylmercury on inorganic mercury. Under the optimized conditions, the detection limit of the proposed method was 1.4 ng L and relative standard deviation of 4.6% for 0.05 μg L Hg(II) was obtained. The linear calibration range was 0.005-0.4 μg L. The accuracy of the method was verified through analysis of the certificated reference materials. The proposed method has been applied in the determination of inorganic Hg in natural water samples.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.aca.2019.04.062 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!