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
FeO@MnO magnetic composite microsphere with hierarchical shells structure has been synthesized through a facile two-step hydrothermal reaction for ultra-trace arsenic enrichment. Scanning electron microscopy and transmission electron microscopy images clearly indicated that the as-synthesized material is a porous hydrangea-like morphology, as well as the size of the composite microspheres and the widths of pore are related to the reaction conditions. The N adsorption-desorption isotherms demonstrated that the specific surface areas and pore volume of FeO@MnO with 8 h hydrothermal synthesis are 121.9260 m g and 0.21 cm g, respectively. The enrichment performance of composites depends on their compositions, and the recovery of As(III) on FeO@MnO with Mn/Fe ratio 1:2 was 1-2.3 times of that on other ratios. In comparison with As(V), experimental data indicated that the prepared composites have faster adsorption rate for As(III). In addition, slurry sampling chemical hydride generation technology can effectively remove and reduce the adsorbed As(III) or As(V) to the gaseous product, thus ensuring that the composite is at least repeated over 5 times. Under the optimized conditions, the detection limit of the proposed method was 2.9 ng L and relative standard deviation of 4.8% for 0.1 μg L As(III) was obtained. The linear calibration range was 0.01-1.5 μg L. The accuracy of the method was verified through analysis of the certificated reference materials. The proposed method has been applied to the determination of inorganic As in natural water samples.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.talanta.2018.06.065 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!