水溶性高分子與界面活性劑固態錯合體之奈米結構與物性研究-Polyacrylamide-DodecylBenzenesulfonicacid系統

• Main Authors: Lucy-Chang, 張敏妮
• Other Authors: Hsin-Lung Chen
• Format: Others
• Language: zh-TW
• Published: 1999
• Online Access: http://ndltd.ncl.edu.tw/handle/55237473331281689333

碩士 === 國立清華大學 === 化學工程學系 === 88 === The solid-state complexes of a flexible polymer, polyacrylamide(PAA),and an amphiphilic surfactant, dodecylbenzenesulfonic acid(DBSA),have been investigated. Complexation between PAA and DBSA occurred via proton transfer from DBSA to the carbonyl group in PAA, giving rise to a "supramolecular comb-like polymer" with ionic bonding. The mesomorphic phase in the complexes was identified by the birefrigent patterns under polarized optical microscopy. Wide angle X-ray diffraction (WAXS) and small-angle X-ray scattering (SAXS) revealed that the complexes microphase separated into a lamellae morphology consisting of alternating polar and nonpolar layers with the long period of ca. 3nm. As the composition x(the average number of DBSA molecules bound with a PAA repeating unit)30.7,the SAXS profiles were characterized by a scattering peak associated with the flat lamellae structure .Multiple scattering peaks were observed at lower degree of complexation(x≦0.6),which were ascribed to the formation of undulated lamellae that organized into a macrolattice with the diffraction patterns observable by SAXS .Preliminary assignments of the lattice planes suggested that the lobes of the undulated lamellae organized into body centered cubic(bcc) or simple cubic(sc) types of unit cell. The glass transition temperature of the polar layers in PAA(DBSA) complexes increased with increasing degree of complexation owing to the stiffening of polymer chains. Complexation with DBSA also enhanced the thermal stability of PAA, where the thermal decomposition temperature can be raised by as much as 35℃.