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
Hydrogenation of CO to form methanol utilizing green hydrogen is a promising route to realizing carbon neutrality. However, the development of catalyst with high activity and selectivity to methanol from the CO hydrogenation is still a challenge due to the chemical inertness of CO and its characteristics of multi-path conversion. Herein, a series of highly active carbon-confining molybdenum sulfide (MoS@C) catalysts were prepared by the in-situ pyrolysis method. In comparison with the bulk MoS and MoS/C, the stronger interaction between MoS and the carbon layer was clearly generated. Under the optimized reaction conditions, MoS@C showed better catalytic performance and long-term stability. The MoS@C catalyst could sustain around 32.4% conversion of CO with 94.8% selectivity of MeOH for at least 150 h.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104557 | PMC |
http://dx.doi.org/10.3390/ijms23095220 | DOI Listing |
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