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Microphase-separated Structure (microphase-separated + structure)
Selected AbstractsSynthesis and characterization of proton-conducting copolyimides bearing pendant sulfonic acid groupsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 8 2005Yan Yin Abstract A series of sulfonated copolyimides (co-SPIs) bearing pendant sulfonic acid groups were synthesized from 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTDA), bis(3-sulfopropoxy) benzidines (BSPBs), and common nonsulfonated diamines via statistical or sequenced polycondensation reactions. Membranes were prepared by casting their m -cresol solutions. The co-SPI membrane had a microphase-separated structure composed of hydrophilic and hydrophobic domains, but the connecting behavior of hydrophilic domains was different from that of the homo-SPIs. The co-SPI membranes displayed clear anisotropic membrane swelling in water with negligibly small dimensional changes in the plane direction of the membrane. With water uptake values of 39,94 wt %, they showed dimensional changes in membrane thickness of about 0.11,0.58, which were much lower than those of homo-SPIs. The proton conductivity , values of co-SPI membranes with ion exchange capacity values ranging from 1.95,2.32 meq/g increased sigmoidally with increasing relative humidity. They displayed , values of 0.05,0.16 S/cm at 50 °C in liquid water. Increasing temperature up to 120 °C resulted in further increase in proton conductivity. The co-SPI membranes showed relatively good conductivity stability during the aging treatment in water at 100 °C for 300 h. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1545,1553, 2005 [source] Gelation Rate Modulation of an , -Cyclodextrin and Poly(ethylene glycol)-Grafted Hyaluronic Acid Solution System by Inclusion Complexation of a Microphase-Separated StructureMACROMOLECULAR RAPID COMMUNICATIONS, Issue 6 2004Tsuyoshi Nakama Abstract Summary: The gelation rate of a poly(ethylene glycol)-grafted hyaluronic acid (PEG- graft -HA) solution with adding , -CD was investigated in term of the microphase separation between the grafted PEG and HA. The gelation rate of PEG- graft -HA exhibiting the microphase-separated structure was two times higher than that of PEG- graft -HA showing a homogeneous miscible state. The formation of microphases by PEG- graft -HA contributes to its rapid gelation upon the addition of , -CDs. [source] Architecture of Polymeric Superstructures Constructed by Mesoscopically Ordered Cubic LatticesMACROMOLECULAR RAPID COMMUNICATIONS, Issue 4 2003Koji Ishizu Abstract Highly monodisperse crosslinked core-shell polymer microspheres could be prepared easily by introducing special crosslinking reagents into the segregated core in block copolymer assembly films. The crosslinked core was stabilized sterically by highly branched shell chains in solution. These microspheres moved like pseudo-latex. The microspheres formed a lattice with a body-centered cubic (BCC) structure near the overlap threshold (C*). This structure changed to a face-centered cubic (FCC) lattice in the bulk region of the films. Photofunctionalized core-shell microspheres were prepared by introducing dithiocarbamate (DC) groups into shell parts by means of polymer reactions, where DC groups could be propagated using vinyl monomers such as methyl methacrylate (MMA) with living radical mechanism. Polymeric superstructure (three microphase-separated structure) films were constructed by graft copolymerization of MMA initiated with photofunctionalized microspheres such as macroinitiators under UV irradiation, exhibiting self-coloring due to Bragg diffraction. These materials can be used for the construction of optical devices such as for the fabrication of light modulators. Photograph of a solution of the microsphere in MMA. [source] Effect of thermomechanical history on the crystallization of poly(ether- block -amide)POLYMER ENGINEERING & SCIENCE, Issue 12 2008Bruno Tavernier The quiescent and flow-induced crystallization of a poly(ether- block -amide) is studied by means of rheo-optical methods. Both optical microscopy and small angle light scattering have been used. The multiblock copolymer has a microphase-separated structure with an order,disorder transition at 180,185°C, as measured with rheometry and SAXS. The number of nuclei, spherulitic growth rates, and the characteristic time scale for crystallization are compared with that of a polyamide of similar molar mass. For the poly(ether- block -amide),containing a majority of amide segments,the growth rates of the spherulites during quiescent crystallization are similar for the block copolymer and the homopolymer, even if the spherulitic structures are not the same. When flow is applied, the two materials behave differently. The flow increased the nucleation density in the homopolymer but not in the block copolymer. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Proton conducting membranes based on poly(vinyl chloride) graft copolymer electrolytesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 7 2008Jin Kyu Choi Abstract The direct preparation of proton conducting poly(vinyl chloride) (PVC) graft copolymer electrolyte membranes using atom transfer radical polymerization (ATRP) is demonstrated. Here, direct initiation of the secondary chlorines of PVC facilitates grafting of a sulfonated monomer. A series of proton conducting graft copolymer electrolyte membranes, i.e. poly(vinyl chloride)- g -poly(styrene sulfonic acid) (PVC- g -PSSA) were prepared by ATRP using direct initiation of the secondary chlorines of PVC. The successful syntheses of graft copolymers were confirmed by 1H-NMR and FT-IR spectroscopy. The images of transmission electron microscopy (TEM) presented the well-defined microphase-separated structure of the graft copolymer electrolyte membranes. All the properties of ion exchange capacity (IEC), water uptake, and proton conductivity for the membranes continuously increased with increasing PSSA contents. The characterization of the membranes by thermal gravimetric analysis (TGA) also demonstrated their high thermal stability up to 200°C. The membranes were further crosslinked using UV irradiation after converting chlorine atoms to azide groups, as revealed by FT-IR spectroscopy. After crosslinking, water uptake significantly decreased from 207% to 84% and the tensile strength increased from 45.2 to 71.5,MPa with a marginal change of proton conductivity from 0.093 to 0.083,S,cm,1, which indicates that the crosslinked PVC- g -PSSA membranes are promising candidates for proton conducting materials for fuel cell applications. Copyright © 2008 John Wiley & Sons, Ltd. [source] Facile synthesis of functional polyperoxides by radical alternating copolymerization of 1,3-dienes with oxygenTHE CHEMICAL RECORD, Issue 5 2009Eriko Sato Abstract We have developed a facile synthesis of degradable polyperoxides by the radical alternating copolymerization of 1,3-diene monomers with molecular oxygen at an atmospheric pressure. In this review, the synthesis, the degradation behavior, and the applications of functional polyperoxides are summarized. The alkyl sorbates as the conjugated 1,3-dienes gave a regiospecific alternating copolymer by exclusive 5,4-addition during polymerization and the resulting polyperoxides decomposed by the homolysis of a peroxy linkage followed by successive , -scissions. The preference of 5,4-addition was well rationalized by theoretical calculations. The degradation of the polyperoxides occurred with various stimuli, such as heating, UV irradiation, a redox reaction with amines, and an enzyme reaction. The various functional polyperoxides were synthesized by following two methods, one is the direct copolymerization of functional 1,3-dienes, and the other is the functionalization of the precursor polyperoxides. Water soluble polyperoxides were also prepared, and the LCST behavior and the application to a drug carrier in the drug delivery system were investigated. In order to design various types of degradable polymers and gels we developed a method for the introduction of dienyl groups into the precursor polymers. The resulting dienyl-functionalized polymers were used for the degradable gels. The degradable branched copolymers showed a microphase-separated structure, which changed owing to the degradation of the polyperoxide segments. © 2009 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 9: 000,000; 2009: Published online in Wiley InterScience (www.interscience.wiley.com) DOI 10.1002/tcr.200900009 [source] | ||||||||||