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101.
Miscibility has been investigated in blends of poly(butylene succinate) (PBSU) and poly(vinyl phenol) (PVPh) by differential scanning calorimetry in this work. PBSU is miscible with PVPh as shown by the existence of single composition dependent glass transition temperature over the entire composition range. In addition, the polymer–polymer interaction parameter, obtained from the melting depression of PBSU using the Nishi–Wang equation, is composition dependent, and its value is always negative. This indicates that PBSU/PVPh blends are thermodynamically miscible in the melt. Preliminary morphology study of PBSU/PVPh blends was also studied by optical microscopy (OM). OM experiments show the spherulites of PBSU become larger with the PVPh content, indicative of a decrease in the nucleation density, and the coarseness of PBSU spherulites increases too with increasing the PVPh content in the blends. 相似文献
102.
Harumi Sato Masahiko Shimoyama Taeko Kamiya Toru Amari Slobodan aic Toshio Ninomiya Heinz W. Siesler Yukihiro Ozaki 《应用聚合物科学杂志》2002,86(2):443-448
Raman spectra have been measured for pellets of five samples of high‐density polyethylene (HDPE), seven samples of low‐density polyethylene (LDPE), and six samples of linear low‐density polyethylene (LLDPE). The obtained Raman spectra have been compared to find out characteristic Raman bands of HDPE, LDPE, and LLDPE. Principal component analysis (PCA) was applied to the Raman spectra in the 1600–650 cm?1 region after multiplicative scatter correction (MSC) to discriminate the Raman spectra of the three different PE species. They are classified into three groups by a score plot of PCA factor 1 vs. 2. HDPE with high density and high crystallinity gives high scores on the factor 1 axis, while LDPE with low density and low crystallinity yields negative scores on the same axis. It seems that factor 1 reflects the density or crystallinity. A PC weight loadings plot for factor 1 shows six upward peaks corresponding to the bands arising from the crystalline parts or all‐trans ? (CH2)n? groups and seven downward peaks ascribed to the bands of the amorphous or anisotropic regions and those arising from the short branches. Partial least‐squares (PLS‐1) regression was applied to the Raman spectra after MSC to propose calibration models that predict the density, crystallinity, and melting points of the polyethylenes. The correlation coefficient was calculated to be 0.9941, 0.9800, and 0.9709 for the density, crystallinity, and melting point, respectively, and their root‐mean‐square error of cross validation (RMSECV) was found to be 0.0015, 3.3707, and 2.3745, respectively. The loadings plot of factor 2 for the prediction of melting point is largely different from those for the prediction of density and crystallinity. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 443–448, 2002 相似文献
103.
The breakup of non-Newtonian emulsion jets into drops was experimentally studied by ejecting both O/W and W/O emulsions vertically downward into stagnant air through nozzles. Breakup lengths of non-Newtonian emulsion jets were found to be almost equivalent to those of Newtonian jets. Experimental breakup data establish that the static surface tension of the oil phase can be used as the surface tension of W/O emulsion jets, whereas the dynamic surface tension of aqueous surfactant solutions is used as that of O/W emulsion jets. Diameters of drops formed from non-Newtonian emulsion jets are in good agreement with the prediction from the stability theory previously developed by the authors. When the rheological index in a power law model is appreciably smaller than unity and the Ohnesorge number is significantly large, however, drop sizes are larger than the prediction because of the profile relaxation in jets. The critical velocity of emulsion jets, either O/W or W/O emulsion, is significantly lower than that of homogeneous Newtonian jets. 相似文献
104.
One-pot polymerization of polyimide from 3,3′,4,4′-biphenyl tetracarboxylic dianhydride (BPDA) and 4,4′-oxydianiline (ODA) was examined. The equilibrium in the polyimide with water was examined in detail in p-chlorophenol solution during the polymerization. The equilibrium constant was expressed by log K = 1.50 + 1433 (1/T). The polymerization reaction is exothermic. The molecular weight increased with decrease of temperature. © 1996 John Wiley & Sons, Inc. 相似文献
105.
Takaho Kaneda Toshio Katsura Kanji Nakagawa Hiroshi Makino Masao Horio 《应用聚合物科学杂志》1986,32(1):3151-3176
The polyimides based on 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA) described in Part I of this series were dissolved in p-chlorophenol and spun into fibers using a coagulating bath of ethanol. The fibers as spun had in general low tenacities and low moduli, but a heat treatment at 300–500°C under tension produced a remarkable increase in strength and modulus, and fibers with a tensile strength of 26 g/den (3.1 GPa) and an initial modulus higher than 1,000 g/den (120 GPa) could be obtained. Thus, the annealed fibers of polyimides are comparable to aramid fibers in mechanical properties. To heating in air and in the saturated steam, the polyimide fibers showed higher resistance than the aramid fibers. The polyimide fibers surpassed the aramid fibers in resistance to acid treatment and ultraviolet (UV) irradiation, but were inferior in resistance to alkali treatment. The annealed fibers of polyimides displayed distinct X-ray diffraction patterns. The chain repeat distance of 20.5 Å determined on the fibers of polyimide prepared from BPDA and o-tolidine, and 20.6 Å determined on the fibers of polyimide derived from BPDA and 3,4′-diaminodiphenyl ether are reasonable when the dimensions of monomeric units and the shapes of the molecular chains are considered. The X-ray reflections of both polyimide fibers were indexed satisfactorily on the basis of postulated unit cells. 相似文献
106.
Toshio Haga 《应用聚合物科学杂志》1981,26(8):2649-2655
The swelling kinetics of crystalline PET films in chloroform–n-hexane mixtures were examined as a function of chloroform concentration. With increasing concentration, the swelling mechanism varied from Fickian to Case II behavior. The dependence of the swelling mechanism on the equilibrium uptake and activation energy for swelling were thoroughly compatible with those presented by other workers. From a viewpoint of superposition of Fickian and Case II swelling, the intermediate swelling between the above two limiting cases was analyzed by Kwei's equation. The magnitude of the diffusion coefficient obtained was remarkably smaller than that presented for the swollen amorphous polymer. The magnitude of the penetration velocity is also discussed in comparison with the data for amorphous polymer. 相似文献
107.
Sakai T Yano H Ohno M Shibata H Torigoe K Utsumi S Sakamoto K Koshikawa N Adachi S Sakai H Abe M 《Journal of oleo science》2008,57(11):629-637
Hexagonal-structured self-assemblies of nanocrystalline (anatase) titania templated by cetyltrimethylammonium bromide (C(16)H(33)N(CH(3))(3)Br; CTAB) (Hex-ncTiO(2)/CTAB Nanoskeleton) were formed after mixing of aqueous solutions containing CTAB spherical micelles and titanium oxysulfate acid hydrate (TiOSO(4).xH(2)SO(4).xH(2)O) as a titania precursor in the absence of any other additives. Formation mechanism of the Hex-ncTiO(2)/CTAB Nanoskeleton was examined in terms of the reaction temperature, titania precursor/CTAB mixing ratio, surfactant type, electrostatic interaction, micelle formation and molecular component. We found that crystal growth of crystalline (anatase) titania (polymorphic crystallization) was promoted with higher temperature and lower titania precursor content in aqueous solutions. In addition, we revealed that the crystalline (anatase) titania was formed in polycation, poly(allylamine hydrochloride ([CH(2)CH(CH(2)NH(2))HCl](n); PAH), and formamide (HCONH(2)) solutions. On the other hand, no titania formation was observed in anionic systems such as sodium dodecyl sulfate (CH(3)(CH(2))(11)OSO(3)Na; SDS) and poly(sodium 4-styrenesulfonate ([C(8)H(7)SO(3)Na](n); PSSS). This indicates that hydrolysis reaction of the titania precursor is initiated by not only cations but also nitrogen atoms in molecules and polymers. Hexagonally structure was formed in only cationic surfactant micellar solutions but not in polycation solutions and formamide. 相似文献
108.
Kuniaki Kawaguchi Kazuhiro Mizuguchi Katsutoshi Suzuki Hideaki Sakamoto Toshio Oguni 《应用聚合物科学杂志》2010,118(4):1910-1920
We investigated the mechanical and physical characteristics of composites composed of polyacetal [alternatively called polyoxymethylene (POM)] and cellulose fiber (CelF) derived from wood pulp [10–52 wt % (9.3–50.1 vol %)] without any fiber surface treatment. The modulus, deflection temperature under load, and thermal conduction coefficient of the POM/CelF composites were effectively enhanced with increasing CelF content, and the composites had an advantage of specific modulus compared to glass fiber (GF)‐filled POM. The flexural modulus of POM/CelF 40 wt % (38.2 vol %) was measured to be about 6 GPa, which was comparable to that of POM/GF 20 wt % (12.1 vol %). In the composites, the CelFs were distributed randomly as monofilaments, and the debonding of the interface between the fibers and POM matrices in the fracture faces was confirmed as less by scanning electron microscopy observation. The POM/CelF composites possessed lower specific wear rates than the POM/GF composites, and they had damping behaviors near that of neat POM. No clear dependence of the melt flow index of the base POM on these characteristics was observed, except on Charpy impact strength. The composites studied here were unique in their performance and ability to be designed in accordance with specific demands, and they could be potential replacements for mineral‐filled and GF‐filled POM composites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
109.
Nanoparticles were prepared by the thermosensitive aggregation of the elastin model polypeptide, (GVGVP)251, and gamma-ray crosslinking. Three different heating processes, “slow heating,” “fast heating,” and “heat shock,” were used
for the aggregation of the peptide, followed by gamma-ray crosslinking. Only the “heat shock” process successfully yielded
stable nanoparticles with diameters of less than ca. 150 nm and a narrow size distribution. Circular dichroism (CD) spectrometry
showed that this polypeptide formed a type-II β-turn structure when the temperature was increased to above the cloudy point
in the case of the “heat shock” process; suggesting that this structure might contribute to stable nanoparticle formation
by gamma-rays. CD spectrometry also suggested that this structure would be affected during the formation of stable crosslinked
particles. 相似文献
110.
The effect of particle agglomeration on sintering has been studied by slipcasting suspensions with pH values ranging from 2 to 11. The rate of densification has been found to depend on the degree of agglomeration. Complete dispersion of alumina primary particles has not been attained through adjustment of pH of suspensions, and agglomerates also remained in the best-dispersed suspension. Elimination of the agglomerates by sedimentation lowered the densification temperature of slip-cast compacts. The grain size-density curve is a function of temperature. High-density and small-grained sintered bodies were obtained by low-temperature long-time firing. 相似文献