国产精品日日摸夜夜添夜夜添无码_亚洲国产成人精品无码区99_蜜桃秘做爰免费网站_国产一区二区不卡视频_精品人人槡人妻人人玩_色777狠狠狠综合伊人_日日夜夜嫩草_国产精品无码久久久_国产精品无码久久久久av_五月天堂婷婷爱_久草资免费资源_羞羞答答综合网_又湿又紧又爽视频免费软件_每日更新日韩精品_欧美精品18videosex性欧_橙人精品在线观看

當(dāng)前位置: 首頁(yè) >> 產(chǎn)業(yè)發(fā)展 >> 正文

A conducting Polymer with Rubbery Elasticity

時(shí)間:2005-04-28
關(guān)鍵詞:conducting Polymer Rubbery Elasticity 來(lái)源:Asia Polymer Symposium(APOSYM/2004)October 10-16

Qi Xue,* Ning Xu, and Wei Chen
Department of polymer Science & Engineering
Nanjing University, Nanjing, 210093, P.R.China

      Conducting polymers, named as “synthetic metals”, are expected to have many applications such as light-emitting diode, large area organic displays, biosensor, DNA-compatible materials, artificial muscle, and other functional materials. But most conducting polymers are composed of rigid π-conjugated chains having hetero-cyclic repeating units, resulting in poor elasticity. In many practical applications, such as artificial muscle, micro-electronics, and some industry purposes, a conductive film with high modulus and rubbery elasticity are required. For improvement of their poor processibility and instability, researchers have employed numerous techniques and conditions for preparation of aromatics to obtain conjugated polymers having good mechanical properties and stable electrical properties. The development has been brought about mainly by the synthesis of new derivatives of the major conducting polymers, and by combining existing conducting polymer with appropriate dopants, and conventional polymers, to form composites, blends, and colloidal dispersion. Blending with block copolymers shows its advantage because the macroscopic phase separation is suppressed and individual important properties of homo-polymers are retained. However, it is unfavorable for the gradual loss of conductivity for the mechanically blends upon elongation and aging in environments. In this paper, we demonstrate a simple idea for modifying the morphology of a conducting polymer film by electro-chemical polymerization of pyrrole in the presence of a tri-block copolymer consisted of a flexible elastomer block and two sulfonated polystyrene blocks. In this experiment, the block copolymer were crosslinked by polypyrrole (PPY) segments, whereas the sulfonated styrene block acted as the dopant for conducting polypyrrole, resulting in a three-dimensional network film with excellent rubber elasticity and manipulated electrical conductivity. Besides, a few orders of magnitude increase in the electrical anisotropy for this rubbery film upon elongation was observed.

      The visco-elastic behavior of PPY-sulfonated SEBS rubber as a function of temperature was measured by DMTA, and the data are illustrated in the lower diagram in the Figure. For comparison DMTA diagrams of sulfonated SEBS elastomer are shown in the upper curves in the following Figure.



The curve of Tan(delta) (E’/E) in the upper diagram shows two peaks at –30 and 130 ℃, corresponding to the glass transitions of the poly(ethylene/butylenes) blocks and sulfonated polystyrene blocks, respectively. In the lower DMTA diagrams in Figure 1, only one Tg peak at –30 ℃ in the curve of Tan (delta) (E’/E) was found. Above Tg, a so-called “rubber plateau” is reached and the polymer is infusible.14,15 The data in Figure 1 show that the tested PPY-sulfonated SEBS film is a typical rubber.

論文來(lái)源:Asia Polymer Symposium(APOSYM/2004)October 10-16