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 we find that polyaniline (PANI), synthesized by aniline chemical polymerization at a surface of template polycarbonate (PC) particles, is significantly different in molecular weight, structural order, oxidation state, and conductivity from a neat PANI. Molecular weight of the PANI phase in the composite (Mw = 158,000) is 1.6 times higher than that of the neat PANI synthesized in the absence of the template particles. Moreover, XRD analysis shows that crystallinity of the PANI phase in the composite is three times higher than that of the neat PANI. Raman spectroscopy indicates that the oxidation level of PANI in the PC/PANI composite is lower than that of the neat PANI. These noticeable changes of the PANI phase properties suggest specific interactions of reagents in the polymerization medium and formed PANI with the template phase as well as an orientation effect of the latter surface. FTIR spectroscopy reveals that hydrogen bonding in the neat doped PANI is weaker than one between -NH- of PANI and C═O of PC at their interface. The discovered differences are supported by the fact that conductivity of the PANI phase in the composite is more than three times higher than that of the neat PANI.
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Source |
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http://dx.doi.org/10.1021/jp311898v | DOI Listing |
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