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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
In this study, spherical α-FeO prepared by the hydrothermal method was used as a template for the first time; LaFeO perovskite catalysts were successfully synthesized by the molten salt method (M-LF-), sol-gel method (S-LF-), and co-precipitation method (C-LF-), respectively. To determine the optimal synthesis method, X-ray diffraction patterns were obtained and showed that single phase LaFeO with good crystallinity was prepared by the molten salt method after calcination at 600 °C for 4 h. SEM and TEM images showed that the M-LF-600 catalyst preserved the spherical structure of α-FeO template. Compared with the catalysts synthesized by the sol-gel method and co-precipitation method, the M-LF-600 catalyst had the highest BET surface area of 16.73 m g. X-ray photoelectron spectroscopy analysis showed that the M-LF-600 catalyst had the highest surface Fe/Fe molar ratio and the best surface oxygen adsorption capacity. The CO oxidation of the LaFeO catalyst demonstrated that the M-LF-600 catalyst had the best catalytic performance.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683013 | PMC |
http://dx.doi.org/10.1039/d2ra05986j | DOI Listing |
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