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 the electronics industry, the efficient recovery and capture of sulfur hexafluoride (SF ) from SF /N mixtures is of great importance. Herein, three metal-organic frameworks with fine-tuning pore structures, Cu(peba) , Ni(pba) , and Ni(ina) , were designed for SF capture. Among them, Ni(ina) has perfect pore sizes (6 Å) that are comparable to the kinetic diameter of sulfur hexafluoride (5.2 Å), affording the benchmark binding affinity for SF gas. Ni(ina) exhibits the highest SF /N selectivity (375.1 at 298 K and 1 bar) and ultra-high SF uptake capacity (53.5 cm g at 298 K and 0.1 bar) at ambient conditions. The remarkable separation performance of Ni(ina) was verified by dynamic breakthrough experiments. Theoretical calculations and the SF -loaded single-crystal structure provided critical insight into the adsorption/separation mechanism. This porous coordination network has the potential to be used in industrial applications.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202207066 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!