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Development of electroless silver plating on Para ‐aramid fibers and growth morphology of silver deposits
Author(s) -
Zhang Huiru,
Zou Xinguo,
Liang Jingjing,
Ma Xiao,
Tang Zhiyong,
Sun Jinliang
Publication year - 2011
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.35332
Subject(s) - aramid , materials science , plating (geology) , composite material , morphology (biology) , scanning electron microscope , chemical engineering , fiber , biology , engineering , genetics , geophysics , geology
The development of a conductive fiber with flame resistance is an urgent concern particularly in national defense and other specialized fields. Aramid fibers ( para ‐ or meta ‐) exihibit high strength and excellent fire resistance. Electroless silver plating on para ‐aramid fibers and growth morphology of silver deposits was investigated in the present work. The surface of para ‐aramid fibers was roughened using sodium hydride/dimethyl sulfoxide to guarantee successful electroless plating. Two complexing agents (ethylene diamine/ammonia) and two reducing agents (glucose/seignette salt) were used for the electroless silver plating bath design. Structure and properties of the resulting silver‐deposited para ‐aramid fibers were evaluated based on scanning electron microscopy, silver weight gain percentage calculation, electrical resistance measurement, crystal structure analysis, and mechanical properties test. The results showed that a higher silver weight gain was advantageous to the improvement of conductivity for the silver‐deposited para ‐aramid fibers. The obtained silver deposit was homogenous and compact. Electroless silver‐plating deposits were considered to be three‐dimensional nucleation and growth model (Volmer–Weber). Black, silver gray, and white deposits appeared sequentially with progressive plating. The breaking strength of silver‐deposited para ‐aramid fibers remained at value up to 44 N. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012