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151.
Jin-Hae Chang Bong-Ku Choi Jae-Hoon Kim Soo-Min Lee Myung-Sik Bang 《Polymer Engineering and Science》1997,37(9):1564-1571
A thermotropic liquid crystalline polymer (LCP) with an alkyl side-group was synthesized. Blends of the LCP with polycarbonate (PC) were prepared by coprecipitatton from a common solvent. The rheological behavior of the LCP/PC blends was found to be very different from that of PC, and significant viscosity reductions were observed in the temperature range of 200–230°C. Blends of different LCP compositions were extruded with different draw ratio from a capillary rheometer. The ultimate tensile strength showed a maximum at a 10 wt% LCP composition in the blends. It decreased for compositions greater the 10 wt% LCP, whereas the initial modulus increased with increasing LCP content. The morphology of the blends was found to be affected by their compositions. Scanning electron microscopy (SEM) studies revealed finely dispersed spherical LCP domains in the PC matrix. The SEM micrographs also showed a poor adhesion between the two phases. 相似文献
152.
Drop-on-demand ink-jet inks made from dyes generally show poor light and wet fastness. A number of studies have been carried out previously to improve the fastness of such inks by introducing novel dyes and new additives. Based on the research results, use of fast dyes could give ink-jet inks with good properties. This study describes new black dyes for aqueous ink-jet inks, which show better light and wet fastness and print quality, compared to an analogous ink formulated from CI Food Black 2. 相似文献
153.
The removal of hydrogen sulfide (H2S) from simulated gas was carried out in a batch type fluidized-bed reactor using natural manganese ore (NMO), which consists
of several metal oxides (MnOx: 51.85%, FeOy: 3.86%, CaO: 0.11%). The H2S breakthrough curves were obtained by changing temperature, gas velocity, initial H2S concentration, and aspect ratio. Moreover, the effects of the particle size and the particle-mixing fraction on H2S removal were investigated in a binary system of different particle size. From this study, H2S removal efficiency increased with increasing temperature but decreased with increasing excess gas velocity. The breakthrough
time for H2S decreased as the gas velocity increased, which leads to reducing gas-solid contacting due to gas bypassing in a fluidized
bed reactor. Improvement of H2S removal efficiency in continuous process can be expected from the results of the binary particle system with different size
in a batch experiment. The NMO could be considered as a potential sorbent in H2S removal. 相似文献
154.
Han Mo Jeong Shang Hoon Lee Kwang Jae Cho Young Tae Jeong Kap Ku Kang Jae Kwon Oh 《应用聚合物科学杂志》2002,84(9):1709-1715
The block copolymer of poly(1‐hexadecene) (PHD) and polypropylene (PP) was effectively synthesized by the sequential polymerization of propylene and 1‐hexadecene by using highly isospecific TiCl3/Cp2Ti(CH3)2 (Cp = cyclopentadienyl). The block copolymers had two separate melting temperatures of constituent blocks. The modulus of PHD–PP block copolymer was enhanced as the content of sequentially polymerized PP block was increased. The elongation at break showed positive deviation at the intermediate compositions from the simple additive values of constituent homopolymers. Shape memory effect which utilizes the crystalline PHD block as a reversible phase and the crystalline PP block as a fixed structure was examined. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1709–1715, 2002; DOI 10.1002/app.10551 相似文献
155.
In a previous study, CETP inhibitory peptide (3 kDa) was isolated from hog plasma. The peptide, synthesized chemically according
to the amino acid sequence of the 3-kDa peptide (designated P28), showed CETP inhibitory activity both in vitro and in vivo [Cho et al. (1998) Biochim. Biophys. Acta 1391, 133–144]. We report herein further unique features of P28 when it was associated with the cholesteryl ester (CE)-donor and-acceptor lipoproteins. Lipoprotein substrates with P28 present in both HDL (as a CE-donor) and LDL (as a CE-acceptor) served as poor substrates, with CE-transfer activity decreased
up to 60% compared to normal substrates without P28. P28 was found to be located in HDL fractions of hog plasma and showed the same electromobility as that visualized by PAGE on
7% polyacrylamide gel under nondenaturing conditions. Addition of apolipoprotein A-1 (apoA-1) or apoB antibody to a normal
CE-transfer mixture did not alter CE-transfer activity. However, addition of apoA-1 or −B antibody to a CETP-inhibition mixture
decreased the inhibitory activity of P28 by ca. 20%. Western blot analysis revealed that P28 was associated only with human and hog HDL among several lipoproteins purified from human, hog, and rabbit. CFTP-inhibition
assays with various lipoprotein substrates revealed that P28 exhibited substrate-specific inhibitory activity. The inhibitory activity of P28 was highly dependent on the type of lipoprotein substrate (whether CE-donor or-acceptor); P28 inhibited CE transfer from HDL to LDL, but it did not inhibit CE transfer from HDL to HDL. 相似文献
156.
Changyong Choi Su Young Chae Tai‐Hyoung Kim Jung Keon Kweon Chong Su Cho Mi‐Kyeong Jang Jae‐Woon Nah 《应用聚合物科学杂志》2006,99(6):3520-3527
Diblock copolymers with different poly(ε‐caprolactone) (PCL) block lengths were synthesized by ring‐opening polymerization of ε‐caprolactone in the presence of monomethoxy poly(ethylene glycol) (mPEG‐OH, MW 2000) as initiator. The self‐aggregation behaviors and microscopic characteristics of the diblock copolymer self‐aggregates, prepared by the diafiltration method, were investigated by using 1H NMR, dynamic light scattering (DLS), and fluorescence spectroscopy. The PEG–PCL block copolymers formed the self‐aggregate in an aqueous environment by intra‐ and/or intermolecular association between hydrophobic PCL chains. The critical aggregation concentrations of the block copolymer self‐aggregate became lower with increasing hydrophobic PCL block length. On the other hand, reverse trends of mean hydrodynamic diameters were measured by DLS owing to the increasing bulkiness of the hydrophobic chains and hydrophobic interaction between the PCL microdomains. The partition equilibrium constants (Kv) of pyrene, measured by fluorescence spectroscopy, revealed that the inner core hydrophobicity of the nanoparticles increased with increasing PCL chain length. The aggregation number of PCL chain per one hydrophobic microdomain, investigated by the fluorescence quenching method using cetylpyridinium chloride as a quencher, revealed that 4–20 block copolymer chains were needed to form a hydrophobic microdomain, depending on PCL block length. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3520–3527, 2006 相似文献
157.
Because silica has strong filler–filler interactions, a silica‐filled rubber compound shows a poor filler dispersion compared to a carbon black‐filled one. Improvement of the filler dispersion in silica‐filled styrene–butadiene rubber (SBR) compounds was studied using low molecular weight polybutadiene (liquid PBD) with the high content of 1,2‐unit. By adding the liquid PBD to the silica‐filled SBR compound, the filler dispersion and flow property are improved. The cure time and cure rate become faster as the 1,2‐unit content of the liquid PBD increases for the compounds containing the liquid PBD. The crosslink density increases linearly with increase in the 1,2‐unit content of the liquid PBD. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3135–3140, 2003 相似文献
158.
The onset of hydrodynamical instability induced by impulsive spin-down to rest in a cylinder containing a Newtonian fluid
is analyzed by using propagation theory. It is well-known that the primary transient swirl flow is laminar, but with initial
high velocities secondary motion sets in at a certain time. The dimensionless critical time Τc to mark the onset of instability is presented here as a function of the Reynolds number Re. Available experimental data indicate
that for large Re deviation of the velocity profiles from their momentum diffusion occurs starting from a certain time Τ≈4Τc. This means that secondary motion is detected at this characteristic time. It seems evident that during Τc⪯Τ⪯4Τc, secondary motion is relatively very weak and the primary diffusive momentum transfer is dominant. 相似文献
159.
Summary The chemical process of preparing poly(vinylchloride)-polypyrrole composite films with high electrical conductivity and transparency has been studied. Pyrrole has been diffused into the poly(vinylchloride) matrix in the swelling medium of n-hexane and acetone mixture. The oxidative polymerization of the diffused pyrrole in the binary solvent system of acetonitrile and methanol gives high conductivity of the polypyrrole as well as the good penetration of the oxidant into the PVC polymer matrix. The analytical testing of the composite film shows the formation of homogeneous mixture of polypyrrole and poly(vinylchloride) conductive layer within the 1.0m of thickness on the film surface. The transparency of the composite film showed about 50–60% at 500 nm. The electrical conductivity of the composite was about 20 s/cm. 相似文献
160.
Seokkyu Lee Wonbong Jang Seunghyuk Choi Kannan Tharanikkarasu Yonggun Shul Haksoo Han 《应用聚合物科学杂志》2007,104(5):2965-2972
Semi‐interpenetrating polymer network (semi‐IPN) membranes based on novel sulfonated polyimide (SPI) and poly (ethylene glycol) diacrylate (PEGDA) have been prepared for the fuel cell applications. SPI was synthesized from 1,4,5,8‐naphthalenetetracarboxylic dianhydride, 4,4′‐diaminobiphenyl 2,2′‐disulfonic acid, and 2‐bis [4‐(4‐aminophenoxy) phenyl] hexafluoropropane. PEGDA was polymerized in the presence of SPI to synthesize semi‐IPN membranes of different ionic contents. These membranes were characterized by determining, ion exchange capacity, water uptake, water stability, proton conductivity, and thermal stability. The proton conductivity of the membranes increased with increasing PEGDA content in the order of 10?1 S cm?1 at 90°C. These interpenetrating network membranes showed higher water stability than the pure acid polyimide membrane. This study shows that semi‐IPN SPI membranes based on PEGDA which gives hydrophilic group and structural stability can be available candidates comparable to Nafion® 117 over 70°C. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 相似文献