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991.
ABSTRACTTwo series of novel side-chain liquid crystal (LC) polysiloxanes grafted with chiral liquid crystalline dimers containing cholesteryl mesogens were synthesised. The chemical structure and LC properties of comonomers and polymers were characterised by FTIR, 1H-NMR, DSC, TGA, POM and XRD. M1 and M2 were chiral nematic (N*) dimers, and M3 was an achiral LC monomer displaying nematic mesophase in a narrow mesomorphic temperature range, while the copolymers exhibited N* mesophase whose mesomorphic temperature ranges were much wider than those of the comonomers. Moreover, the glass transition temperatures and isotropization temperatures of the polymers all decreased with decreasing the dimer components. Reflection spectra showed that Pa series tend to attain wide-band selective reflection at long wavelengths, while Pb series were more potential at short wavelengths with narrow bandwidths. Decreasing the dimer components led the wavelength of the selective reflection to blue shift, which was an abnormal phenomenon in chiral mixture system. 相似文献
992.
ABSTRACTOptical diffusers are promising diffusing materials in the optical devices such as monitors, projectors, fibre optics, light-emitting diode (LED) systems and liquid crystal displays (LCDs). We report optical diffusers comprising uniformly distributed nano-sized polymer balls/nematic liquid crystals (LCs) by ultraviolet (UV) click reaction of ene monomer and thiol monomer. By optimising the mass ratio 1:1 of ene and thiol, of which the average diameter of the corresponding nano-sized polymer balls is about 900 nm, relatively high optical transmission and haze with 88.99% and 94.49% are yielded, respectively. Furthermore, by controlling the curing time, the average diameter of nano-sized polymer balls can be reduced to 810 nm, and the developed film exhibits high transmission (98.49%) without sacrificing the high haze (91.77%). This paper demonstrates that UV click reaction is an economical approach to fabricate optical diffusers in a controllable manner. 相似文献
993.
Sambhu Bhadra 《European Polymer Journal》2008,44(6):1763-1770
Substitution in aniline has tremendous effect in the synthesis of poly(substituted anilines) as well as in their properties. In this investigation polyaniline (PANI), poly(m-nitro aniline) (PMNA), poly(m-amino phenol) (PMAP) and poly(o-ethyl aniline) (POEA) were synthesized by oxidative polymerization under identical conditions. Different properties were measured and compared with PANI to find out the presence of electron donating -OH group, electron withdrawing -NO2 group and less effecting ethyl group on the properties of poly(substituted anilines). It was found that presence of any type of substitution in the benzene ring of aniline increases the solubility of the resulted polymer but reduces the yield, degree of polymerization, thermal stability, electrical and thermal conductivity. The colors, bulk density, particle size, percentage of crystallinity vary considerably depending on the nature of substitution. 相似文献
994.
Jichang Feng 《European Polymer Journal》2008,44(10):3314-3319
A hyperbranched copolymer (HTP) containing triphenylamine and divinyl bipyridyl units has been synthesized via Heck coupling reaction from 5,5′-divinyl-2,2′-bipyridyl and tris(4-bromophenyl)amine. The polymer had a number-average molecular weight of 1895 and a weight-average molecular weight of 2315, and was readily soluble in common organic solvents, such as THF, DMF and chloroform. The chemical structure of HTP was confirmed by FT-IR, 1H NMR. Its thermal, electrochemical and optical properties have been investigated. The thermal analysis revealed that the polymer had a good thermal stability with the onset decomposition temperature at ca. 267 °C. The Uv-vis absorption and photoluminescence (PL) spectra exhibited that the Stokes shift between the absorption and emission of HTP was relatively large: 103 for HTP solution and 135 nm for HTP film. The electrochemical analysis showed that the electrochemical band gap of HTP was 0.92 eV. The fluorescence of the polymer in solution can be quenched by various transition metal ions and HTP showed different sensitivity in transition metal ions sensing. 相似文献
995.
Polymer materials used in railway field are degraded by environmental factors such as thermal, oxidative, photolytic, hydrolytic, and mechanical. The expected service life of the polymer materials used in railway field is approximately 20 years that is relatively long period for the polymer material; therefore, respective degradation factors should be well considered. Some of the degradation conditions indicate similar mechanism. The oxidative reaction was seen in every degradation conditions under air atmosphere. The hydrolytic reaction was mainly observed in chemical and biological degradations. The degradation behavior of the polymer material was analyzed by various methods. FTIR, thermal analysis (TG, DSC), and molecular weight determination were mainly applied for its purpose. However, the degradation mechanism of practical products made of polymer material was insufficiently studied and the exchange criteria of the products depended on the visual inspection without the suitable degradation analysis not only in the railway field but also in other commercial and industrial fields. In addition, most of the methods to analyze degradation of polymer material are performed on the standard specimen forms. For the installed product, some kinds of damage are generated through the sample collection process; therefore, the damaged products have to be exchanged for brand new ones or repaired totally to be used for more period. Moreover, it is hard to suspend the railway service for the degradation analysis of polymer products. From these backgrounds, the prospect of degradation analysis related to polymer materials used in railway field was proposed. 相似文献
996.
Theoretical study on the geometries and electronic properties of new conjugated compounds based on thiophene and phenylene was carried out. The theoretical ground-state geometries and electronic structures of the studied molecules were obtained using the density functional theory (DFT) method at B3LYP level with 6-31G(d) basis set. The electronic properties were determined by ZINDO/s, CIS/3-21G(d), and TD//B3LYP/3-21G(d) calculations performed on the B3LYP/6-31(d) optimized geometries. The effects of the ring structure and the substituents on the geometries and electronic properties of these materials were discussed. The results of this study indicate how the electronic properties can be tuned by the backbone ring or side group and suggest these compounds as good candidates for opto-electronic applications. 相似文献
997.
多嵌段聚醚氨酯脲为基质的新型高分子固态离子导体 总被引:2,自引:0,他引:2
本文合成了一系列聚乙二醇型多嵌段聚醚氨酯脲,而且用这类聚醚氨酯甩与高氯酸锂制得了一种新型的高分子固态离子导体复合物。在室温和50℃之间,其电导率比聚环氧乙烷为基质的固体电解质的高一到二个数量级,它还具有优良的综合性能。因此,对于室温薄膜蓄电池来说,这种新型的固体电解质是一类良好的候选材料。 相似文献
998.
The morphology and the crystallization behavior of blends of linear low density polyethylene (LLDPE) with an experimental sample of a semiflexible liquid crystalline polymer (SBH 112 by Eniricerche, Italy) have been studied by differential scanning calorimetry (DSC), polarized optical microscopy (POM) and scanning electron microscopy (SEM). The blends possess a two-phase morphology, due to immiscibility of the two components. SEM observations show that dispersion of the minor SBH phase is favored at low (相似文献
999.
Kubo T Hosoya K Nomachi M Tanaka N Kaya K 《Analytical and bioanalytical chemistry》2005,382(7):1698-1701
A molecularly imprinted polymer was prepared using a water-soluble crosslinking agent. An ionic complex was utilized as the assembly for the template molecule and the functional monomer, and water as porogenic solvent during preparation of the imprinted polymer. The results of chromatographic evaluations for the prepared polymer suggested that the polymer had much lower hydrophobicity compared with usual octadecyl group bonded silica or the usual molecular imprinted polymer prepared from ethyleneglycol dimethacrylate, and the selective recognition ability for template molecule in the completely aqueous condition. 相似文献
1000.
N. Kruszewska 《Physica A》2010,389(16):3053-3068
In-plane (bio)matter aggregations of amphiphilic nature are modeled extensively by Monte Carlo simulation in their natural entropic contexts. The modeling starts by designing the aggregations at a molecular level, pointing to its well-known configuration vs conformation character. Then, the conformational behavior is distributed over the aggregations obtained, with the aim of revealing their main sol-gel type (viscoelastic) effects. The passage between the resulting sol and gel phases is not controlled by a scan in the temperature domain, on the contrary, the control parameter is selected to be the hydrophobic-interaction strength while the temperature remains unchanged. The distribution of ordered fringed micelles, and the overall crystalline inclusions of the gel phase, suggested a first-order phase change, reasonably conceivable in terms of Avrami-Kolmogorov formalism for such hydrophobic-force driven and percolation-in-nature systems. A phase transition diagram has been presented as a novel proposition to discern between sol vs gel phases. As specific results, also of high experimental value, a damped-oscillating cluster-involving effect on the resulting hydrophobic-polar matrices has been detected and analysed. Other additional intermolecular-sharing entropy-influenced effects on clustering, as seen in terms of chain-to-chain connectivities, have been addressed as being of sufficient relevance to the gelation mechanism described. The microcrystalline inclusions downgrade to some extent the overall picture of entropy-affected gelation, being all together suitable for experimental check-out. 相似文献