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
The surface hydrophobicity of solid particles plays a critical role in the nucleation of gas hydrate formation, and it was found that the hydrophobic surface will promote this nucleation process, but the underlying mechanism is still unveiled. Herein, we proposed for the first time our new theory that the formation of methane nanoscale gas bubbles on the hydrophobic surface provides the nuclei sites for further formation of methane hydrate. First, we studied the effect of hydrophobicity of particles on the nucleation of hydrate. It was found that the hydrophobic graphite and silica particles would promote the nucleation of hydrate, but the hydrophilic silica particles did not promote the methane hydrate nucleation. Then, we designed the atomic force microscopy experiment to explain this mechanism from a nanometer scale. The results showed that the methane nanobubbles were formed on the hydrophobic highly ordered pyrolytic graphite surface, but they were hard to form on the hydrophilic mica surface. These results indicated that the methane nanobubbles on the hydrophobic surface could provide the gas hydrate nucleation sites and may induce a rapid nucleation of methane hydrate.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acs.langmuir.8b01900 | DOI Listing |
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