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聚氧乙烯-聚氧丙烯-聚氧乙烯(PEO-PPO-PEO)嵌段共聚物是一类重要的非离子表面活性剂,在选择性溶剂中可以自组装成多种形貌的介观结构。对PEO-PPO-PEO嵌段共聚物在水溶液中自组装行为进行了综述,介绍了其自组装行为的实验研究技术;阐明了嵌段共聚物构型、分子量、温度、浓度、添加剂等因素对PEO-PPO-PEO嵌段共聚物聚集行为的调控和作用机理;介绍了嵌段共聚物自组装特性的热力学模型、分子模拟及计算机预报等研究方法和研究进展;重点介绍了PEO-PPO-PEO嵌段共聚物在介孔材料制备、药物载体、生物大分子分离、嵌段共聚物修饰等方面的应用。 相似文献
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嵌段共聚物通过自组装可以形成特定的周期性纳米结构,然而这些有限种类的体相结构却无法有效满足实际应用中的众多需求.为丰富嵌段共聚物自组装的纳米结构库,几何受限的引入是最为有效的方法之一.几何受限改变了体相结构的平移对称性,嵌段高分子为了缓解这一破坏带来的结构受挫,从而形成更多的新相结构.本文以AB两嵌段高分子为例,从本体... 相似文献
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针对丙烯腈-丁二烯-苯乙烯(ABS)树脂中的橡胶粒子相形态难以精确调控的问题,提出采用可逆加成断裂链转移(RAFT)乳液聚合合成苯乙烯-丙烯腈无规共聚物和苯乙烯-丙烯腈/丁二烯嵌段共聚物,并通过共混制备嵌段型ABS树脂,研究嵌段共聚物分子结构对材料相形态和机械性能的影响。结果表明,通过乳液共混可制得橡胶粒子均匀分散的ABS树脂,与市售产品相比,采用两嵌段共聚物为增韧剂的嵌段型ABS树脂具有优异的综合性能,将增韧剂改为三嵌段共聚物,材料的拉伸断裂韧性能进一步提升,但缺口冲击性能下降明显。 相似文献
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CV Kulkarni 《Nanoscale》2012,4(19):5779-5791
Lipid crystallization is ubiquitous in nature, observed in biological structures as well as in commercial products and applications. In a dehydrated state most of the lipids form well ordered crystals, whereas in an aqueous environment they self-assemble into various crystalline, liquid crystalline or sometimes macroscopically disordered phases. Lipid self-organization extends further to hierarchical levels including structured emulsions and nanostructured particles. Many consumer products including cosmetics, foods and medicines account for such lipid architectures. Cell membranes primarily consist of planar lipid bilayers; however sub-cellular biomembranes are more of a convoluted type. Some of the biological entities have lipids in truly crystalline form; yet liquid crystalline lipid phases are prevalent, in general. Crystallization of fats - triglyceride lipids - has been relatively well documented and reviewed more often, but this review features other areas where lipid organization is crucial and diverse. Some recent advances along with a few explicit examples of model lipid phases and biological evidences are also reported. 相似文献
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Summary Liquid crystalline/conducting polymer blends have been prepared. The conductingpolymer [poly(2,5-dimethoxyphenylene vinylene)]
retards the liquid crystallinity of the liquid crystalline polymer (hydroxypropyl cellulose), while the liquid crystalline
polymer reduces the conductivity of the conducting polymer. However, blends with 17% conducting polymer were both liquid crystalline
and conductive.
Dedicated to Prof. Dragutin Fleš on the occasion of his 70th birthday 相似文献
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We synthesized a ferroelectric liquid crystalline monomer (4‐[4′‐(7‐octeneloxy)benzoyloxy]benzoate‐2‐methylbutyester, OBBM) possessing both carboxyl p‐benzolxybenzoate and carboxyl (s)‐(‐)‐2‐methylbutylester as a mesogenic group in its side chain. The liquid crystalline and styrene monomers were employed to make matrices of microspheres prepared by dispersion, suspension, or emulsion polymerization. In this study, we investigated, in detail, physicochemical properties, thermal responses, and electrooptical responses of the microspheres possessing liquid crystalline abilities. The ferroelectric liquid crystalline monomer OBBM had a thermotropic liquid crystalline ability, two‐phase transition temperatures, and a Smectic C* texture, which is characteristic of ferroelectric liquid crystalline substances. The microspheres prepared also exhibited a liquid crystalline ability, and the phase‐transition temperatures toward the liquid crystalline segments into the microspheres prepared by copolymerizing the liquid crystalline and styrene monomers could be decreased with increasing of the styrene monomer. Furthermore, we found that the microspheres remarkably exhibited electrooptical responses at about 8 V. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 2490–2499, 2001 相似文献
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A series of liquid crystalline polyrotaxanes containing azobenzene mesogenic moieties (AzoPR) with different length of spacer
were synthesized, and the relationship between the spacer length and the liquid crystalline behavior was investigated. The
molecular characterization of the AzoPR was performed with 1H NMR, FT-IR, and gel permeation chromatography. The thermal stability was investigated via thermogravimetric analysis. Their
phase structures and liquid crystalline properties were studied by differential scanning calorimetry, polarized optical microscopy
and wide-angle X-ray diffraction. The experimental results suggested that AzoPR with spacer length of 2 and 4 failed to show
the liquid crystalline behavior, and AzoPR with spacer length of 6 showed the columnar nematic phase. However, when the spacer
length increases to 11, the columnar nematic phase formed, meanwhile, the liquid crystalline domains with high ordered structure
were developed by azobenzene mesogens. 相似文献
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Attempts to extend the IPN technology to liquid crystalline polymer (LCP) systems have been made in search for a new approach for enhancing the compatibility of liquid crystalline polymer with engineering thermoplastics. A new type of interpenetrating polymer network based on liquid crystalline polymer : semi‐interpenetrating liquid crystalline polymer network comprising liquid crystalline polymer PET/60PHB (LCP) and crosslinked polystyrene (PS) (for short: semi‐ILCPN LCP/PS) has been successfully prepared. The compatibility and thermal properties of the semi‐ILCPN LCP/PS with different amount of crosslinking agent were investigated by FTIR, SEM, DSC, and TGA, respectively. Furthermore, the possible application of the semi‐ILCPN LCP/PS as a new kind of compatibilizer in PPO/LCP blends was also studied and discussed. Well‐compatibilized PPO/LCP composites with considerably improved mechanical properties were obtained. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 1141–1150, 2000 相似文献
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We investigated liquid crystallization of liquid crystalline polyester BB-5 during isothermal annealing by digital high-fidelity microscope and light scattering. A liquid crystalline spherical domain having a radius of micrometers appeared by annealing at around 180 °C. The domain grew dendritically in all directions. Neighboring liquid crystalline regions coalesced and then interconnected. The interconnected structure changed to a co-continuous two-phase structure with increasing ordering of the liquid crystalline phase, and the interface between the liquid crystalline phase and the isotropic phase became smoother over time. Liquid crystallization stopped before volume filling the whole space, and the liquid crystalline phase and isotropic phase coexisted. The liquid crystalline region became narrower with an increase in the temperature of the liquid crystallization. Such structural development is different from the liquid-liquid phase separation via spinodal decomposition, and it may be attributed to the segregation of non-liquid crystallizable low molecular weight molecules from the growth front by fractionation of the molecular weight distribution during the liquid crystallization in terms of the instability of the diffusion-controlled interface. 相似文献
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Jui-Hsiang Liu Yu-Kan Wang Chien-Chih Chen Po-Chih Yang Feng-Ming Hsieh Yi-Hong Chiu 《Polymer》2008,49(18):3938-3949
A series of novel side chain liquid crystalline polyacrylates with pendant chiral groups were synthesized. It was found that monomers with electron releasing -OC4H9 terminal groups seem beneficial for the formation of liquid crystalline phases. Copolymerization of the monomers was carried out and the physical properties of the copolymers were investigated. All synthesized polymers revealed liquid crystalline phases and appeared highly thermally stable with decomposition temperatures (Td) at 10% weight loss greater than 384 °C and about 50% weight loss occurred beyond 442 °C under nitrogen atmosphere. Two miscible chiral compounds were also synthesized and used as chiral dopants to induce cholesteric liquid crystalline phases of polymers. Liquid crystalline phases of the polymers were investigated using DSC and XRD, and confirmed with POM technique. The optical properties of the induced cholesteric liquid crystalline polymers were investigated using UV-vis spectrometer. The appearance and the color variation of the polymer films before and after UV irradiation were also investigated. Typical helical morphology of the cholesteric liquid crystalline film was analyzed by SEM technique. 相似文献
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Elizabeth J. Robinson Elliot P. Douglas John J. Mecholsky 《Polymer Engineering and Science》2002,42(2):269-279
The fracture toughness of a liquid crystalline epoxy was compared with that of a standard bisphenol‐A based epoxy to understand how both the liquid crystalline structure and the crosslink density affect fracture toughness. For the liquid crystalline epoxy, the liquid crystalline domain size decreased with increasing temperature of cure and away from the stoichiometric formulation. Quantitative fractography showed that there is a competition between the liquid crystalline domain structure and the stoichiometry in determining the fracture toughness. At some cure conditions the effect of the domains is dominant. When the cure conditions are adjusted to reduce the domain size, the domains become too small to affect the fracture toughness, and thus the effect of the stoichiometry is dominant. The result is that the formation of liquid crystalline structure only increases the fracture toughness relative to that of a traditional epoxy at and near the stoichiometric formulation. 相似文献