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
In this work, a series of innovative metal oxide impregnated waste-derived activated carbons (MO/AC) was synthesized and used to purify the simulated biohydrogen based on the concept of CO removal from the gas stream. Effects of metal oxide types (CaO, SrO and MgO) and contents of the best metal oxides on the morphology and the CO adsorption capacity from the biohydrogen were investigated. It was found that both metal oxide types and contents played an important role on the adsorbent textural property and surface chemistry as well as the CO adsorption capacity. Among all synthesized adsorbent, the MgO-impregnated AC with 12 wt.% MgO (12MgO/AC) exhibited the highest CO adsorption capacity of around 94.02 mg/g. With this successive adsorbent, the biohydrogen with the H purity higher than 90 mol% can be achieved from the gas stream with 50 mol% CO for the first 2 min of adsorption period in a fixed bed reactor. The mechanism of CO adsorption occurred via a combined process of the physisorption and chemisorption. Besides, the 12MgO/AC exhibited a high recyclability after several repetitive adsorption/desorption cycles.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033907 | PMC |
http://dx.doi.org/10.1038/s41598-023-31723-4 | DOI Listing |
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