Summary: In this work, blends of monomer casting polyamide 6 (MCPA6) and acrylonitrile‐butadiene‐styrene (ABS) were successfully prepared by in situ polymerization via the application of ε‐caprolactam as a reactive solvent. The morphology and thermal properties of MCPA6/ABS were investigated by means of wide angle X‐ray diffraction (WAXD), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM), respectively. The domain sizes of the ABS phase in MCPA6/ABS blends were much finer than those in corresponding polyamide 6 (PA6)/ABS blends prepared by simple melt blending. With an increased amount of ABS in MCPA6, the melt enthalpy (ΔHf), the rate of crystallization (Tc) and the degree of crystallinity (Xc(DSC)) of MCPA6 in MCPA6/ABS blends were all decreased. The degree of supercooling (ΔTd) showed a contrary trend. However, the melting temperatures of these blends were almost unchanged. All the results could be attributed to in situ polymerization and the hydrolysis reaction of ABS that occurred during the polymerization process. Furthermore, WAXD results showed that only α‐form crystals existed in the MCPA6/ABS blends, despite the ABS content and heat treatment.
SEM micrograph of the fractured surface of an MCPA6/ABS blend with an ABS content of 20 wt.‐% (×10 000). 相似文献
Summary: Silica sols were first prepared based on different ratios of tetraethoxysilane (TEOS) and methyltriethoxysilane (MTES) by an acid‐catalyzed sol–gel process, and then incorporated into acrylic‐based polyurethanes. The structures and morphologies of silicone‐oxo clusters were studied by 29Si NMR, SAXS, and scanning electron microscopy (SEM), whereas the mechanical properties of polyurethane/silica hybrids were characterized by DMA and tensile tests. The silicone‐oxo clusters in both silica sol and polyurethane hybrids became denser and larger at a higher molar ratio of TEOS/MTES and higher silica content, and the silica‐oxo clusters of polyurethane/silica hybrids even became more compact and larger than those of silica sols, increasing the elastic modulus and tensile strength of polyurethane/silica hybrids.
Typical structure of silica sol prepared from the hydrolysis and condensation of TEOS and MTES with acid as the catalyst. 相似文献
Abstract. The purpose of the present study was to examine the changes in maximum voluntary isometric contraction (MVC) in the contralateral
untrained limb during unilateral resistance training and detraining, and to examine the factors inducing these changes by
means of electrophysiological techniques. Nine healthy males trained their plantar flexor muscles unilaterally 4 days·week–1 for 6 weeks using 3 sets of 10–12 repetitions at 70–75% of one-repetition maximum a day, and detrained for 6 weeks. Progressive
unilateral resistance training significantly (P<0.05) increased MVC, integrated electromyogram (iEMG), and voluntary activation in the trained and contralateral untrained
limbs. The changes in MVC after training were significantly correlated with the changes in iEMG in both limbs. No significant
changes occurred in MVC, voluntary activation, and iEMG in the contralateral limb after detraining. The changes in MVC after
detraining did not correlate with the changes in voluntary activation or iEMG in either limb. Training and detraining did
not alter twitch and tetanic peak torques in either limb. These results suggest that the mechanisms underlying cross education
of muscular strength may be explained by central neural factors during training, but not solely so during detraining.
Electronic Publication 相似文献
Due to the nonlinear, viscoelastic material properties of brain, its mechanical response is dependent upon its total strain history. Therefore, a low strain rate, large strain will likely produce a tissue injury unique from that due to a high strain rate, moderate strain. Due to a lack of current understanding of specific in vivo physiological injury mechanisms, a priori assumptions cannot be made that a low strain rate injury induced by currently employed in vitro injury devices is representative of clinical, nonimpact, inertial head injuries. In the present study, an in vitro system capable of mechanically injuring cultured tissue at high strain rates was designed and characterized. The design of the device was based upon existing systems in which a clamped membrane, on which cells have been cultured, is deformed. However, the present system incorporates three substantial improvements: (1) noncontact measurement of the membrane deflection during injury; (2) precise and independent control over several characteristics of the deflection; and (3) generation of mechanical insults over a wide range of strains (up to 0.65) and strain rates (up to 15s–1). Such a system will be valuable in the elucidation of the mechanisms of mechanical trauma and determination of injury tolerance criteria on a cellular level utilizing appropriate mechanical injury parameters. 相似文献
Summary: After the condensation polymerization of benzoguanamine (BGA) and pyromellitic dianhydride (PMDA) under microwave irradiation, the resulting p‐π conjugate poly(amic acid) was grafted via the azo coupling reaction. The obtained side‐chain polymers were further grafted with TDI‐aliphatic alcohol derivatives and TDI‐aniline derivatives. The third‐order NLO coefficient and response time of PAA and graft polymers were measured by degenerated four wave mixing (DFWM) technique and their fluorescent properties were also investigated. All of the graft polymers have larger NLO coefficients and film‐formability than PAA. Their fluorescent properties were also changed by the different electronic effect of the side‐chains. The influences of the introduction of side‐chains, the side‐chain length and the electronic effect of the substituting groups on the azobenzol side‐chain to both optical properties of the polymers by varying the conjugation degree were investigated.