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71.
A. V. Kukhto É. É. Kolesnik A. L. Gurskii E. V. Lutsenko K. A. Osipov V. N. Pavlosvskii Yu. V. Grazulyavichyus A. Nedelcheva I. K. Grabchev 《Journal of Applied Spectroscopy》2007,74(6):915-920
We have studied the effect of the intensity of the exciting radiation and the temperature on the emission properties of two
kinds of thin-film samples based on blends of two types of organic electroactive materials: polyfluorene + iridium triphenylpyridinate
and polyepoxypropylcarbazole + zero-th order PAMAM dendrimer with eosin. We have shown that an increase in the excitation
intensity leads to an increase in the intensity of the luminescence of the polymer matrices and the iridium complex up to
a power density of 300 kW/cm2, and the emission of the dendrimer is rapidly saturated and does not return to the initial value when the excitation level
decreases. Heating up to 170°C followed by cooling causes an increase in the intensity for all the components except the dendrimer.
The data obtained show that annealing is an important method for improving the emission efficiency of the proposed thin-film
structures, due to a change in the packing of the activator molecules in the polymer matrix leading to more efficient transfer
of the excitation energy. Molecules of the studied dendrimer are not stable when exposed to optical radiation and temperature.
__________
Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 6, pp. 820–825, November–December, 2007. 相似文献
72.
The data presented for polysulfone in o-dichlorobenzene support previous observations on other systems in which the heats of solution decrease linearly with increasing temperature of measurement. Consistent with similar measurements on polycarbonate and polyphenylene oxide, a dramatic slope change from 0.078 cal/g-C° below 120°C to 0.019 cal/g-C° above 120°C occur for the data on polysulfone. The source of these heats is due primarily to the enthalpy difference between the solid polymer and its corresponding liquid amorphous state at the measurement temperature since the heats of mixing are rationalized to be small. 相似文献
73.
The effects of adding A–B diblock copolymer to a polymer blend (A/B) on phase‐separation kinetics and morphology have been investigated in a fixed shallow‐quench condition (ΔT = 1.5 °C) by in situ time‐resolved light scattering and phase‐contrast optical microscopy. A shear‐quench technique was used in this study instead of a conventional temperature‐quench method. Mixtures of nearly monodisperse low relative‐molecular masses of polybutadiene (Mw = 2.8 kg/mol), polystyrene (Mw = 2.6 kg/mol), and a near‐symmetric butadiene–styrene diblock copolymer (Mw = 6.3 kg/mol) as an interfacial modifier were studied. We observed that the addition of the diblock copolymer could either retard or accelerate the phase‐separation kinetics depending on the concentration of the diblock copolymer in the homopolymer blends. In contrast to the conventional temperature quench, we observed complex phase‐separation kinetics in the intermediate and late stages of phase separation by the shear‐quench technique. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 819–830, 2001 相似文献
74.
Defeng Wu Yisheng Zhang Lijuan Yuan Ming Zhang Weidong Zhou 《Journal of Polymer Science.Polymer Physics》2010,48(7):756-765
Poly(ε‐caprolactone)/polylactide blend (PCL/PLA) is an interesting biomaterial because the two component polymers show good complementarity in their physical properties. However, PCL and PLA are incompatible thermodynamically and hence the interfacial properties act as the important roles controlling the final properties of their blends. Thus, in this work, the PCL/PLA blends were prepared by melt mixing using the block copolymers as compatibilizer for the studies of interfacial properties. Several rheological methods and viscoelastic models were used to establish the relations between improved phase morphologies and interfacial properties. The results show that the interfacial behaviors of the PCL/PLA blends highly depend on the interface‐located copolymers. The presence of copolymers reduces the interfacial tension and emulsified the phase interface, leading to stabilization of the interface and retarding both the shape relaxation and the elastic interface relaxation. As a result, besides the relaxation of matrices (τm) and the shape relaxation of the dispersed PLA phase (τF), a new relaxation behavior (τβ), which is attribute to the relaxation of Marangoni stresses tangential to the interface between dispersed PLA phase and matrix PCL, is observed on the compatibilized blends. In contrast to that of the diblock copolymers, the triblock copolymers show higher emulsifying level. However, both can improve the overall interfacial properties and enhance the mechanical strength of the PCL/PLA blends as a result. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 756–765, 2010 相似文献
75.
应用红外差谱技术测定二元混纺纤维的种类 总被引:1,自引:0,他引:1
应用傅立叶变换红外光谱测定六种二元混纺纤维,得到了清晰的红外光谱图,应用计算机差谱技术得到高质量的差谱结果,准确判明了混纺纤维的种类。本方法不需要对混纺纤维进行分离、预处理,制样简单、准确度好、操作简便。 相似文献
76.
N. C. Das H. Wang J. Mewis P. Moldenaers 《Journal of Polymer Science.Polymer Physics》2005,43(24):3519-3533
Viscoelastic properties of model immiscible blend were studied here under steady state condition at different initial conditions and transient flow conditions. The flow‐induced microstructure has been studied on these model blends. For this system, the elastic properties of the blend are mainly governed by the interface. Measurement of the dynamic modulus and of the first normal stress difference, both reflecting this enhanced elasticity, have been used to prove the blend morphology. The dynamic moduli after cessation of shear flow, the mean diameter of the disperse phase as generated by the shear flow, have been calculated using the model of Palierne. A procedure based on a direct fitting of the dynamic moduli with the model is compared with the one that uses a weight relaxation spectrum. On the other hand, the steady state normal stress data have been related to the morphology of the blend by means of Doi and Ohta model. The specific interfacial area is found to be inversely proportional to the ratio of interfacial tension over shear stress for the blend. The flow behavior during transient shear flow was also discussed. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 3519–3533, 2005 相似文献
77.
78.
Tadashi Yokohara 《European Polymer Journal》2008,44(3):677-685
Structure and properties are studied for binary blends composed of poly(lactic acid) (PLA) and poly(butylene succinate) (PBS). The rheological measurements in the molten state reveal that the entanglement molecular weight of PLA is lower than that of PBS. Further, the interfacial tension of the immiscible blend system is evaluated employing a rheological emulsion model and found to be 3.5 [mN/m]. Moreover, thermal analysis directly detects that addition of PBS enhances the crystallization of PLA even though PBS is in a molten state. Further, the cold-crystallization for quenched blends occurs at lower temperature than that for a quenched PLA. This would be attributed to the nucleating ability of PBS, leading to generation of PLA crystallites during the quench operation. 相似文献
79.
Zhaoju Yu Yuanqin Jiang Weiwei Zou Jiangjiang Duan Xiaopeng Xiong 《Journal of Polymer Science.Polymer Physics》2009,47(17):1686-1694
Blend films from cellulose and konjac glucomannan (KGM) in room temperature ionic liquid 1‐allyl‐3‐methylimidazolium chloride were satisfactorily prepared by coagulating with water. The composition of the blend films was gravimetrically analyzed, and the compatibility of the two natural polymers was characterized by Fourier transform infrared spectroscopy and wide‐angle X‐ray diffraction. The results indicate good compatibility and strong interactions between cellulose and KGM, resulting in almost no loss of the water‐soluble KGM from the blend films even after the water coagulating and washing. However, microstructure analyses portrayed phase separations in the blend films, namely, egg‐like new phase particles were embedded in a continuous matrix base (MB). Phase diagram analysis and differential scanning calorimetry of the phase inversion coagulation process suggest that relative low molecular mass part of both cellulose and KGM formed the continuous MB, whereas the egg‐like new phase particles were super patterns of relative high molecular mass of both polymers, which played an important role in strengthening the blend material. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1686–1694, 2009 相似文献
80.
Inorganic nanoparticles are widely used to improve space charge behavior, DC breakdown strength and other electrical properties of polymer insulating materials, but the uniform distribution of inorganic nanofillers in matrix is difficult due to their agglomeration and bad compatibility with the polymeric matrix. In this paper, polypropylene (PP)/polystyrene (PS) blends were prepared to suppress space charge accumulation and improve DC breakdown strength. Polypropylene-g-polystyrene (PP-g-PS) graft copolymer was used as compatibilizer to improve the compatibility of PP matrix and PS filler. The evolution of microstructure of PP/PS blends were investigated by scanning electron microscope (SEM), the space charge distributions were measured by a pulsed electro-acoustic (PEA) system, and DC breakdown strength was also tested. The morphologies show that the size of PS particles reduced to 310 nm when the content of PP-g-PS graft copolymer increased to 24 wt%, and the interaction between PP matrix and PS particles enhanced. The presence of PS particles in all PP/PS blends suppressed the space charge accumulation compared to neat PP, but the DC breakdown strength in uncompatibilized blend was lower than neat PP. The increasing of content of PP-g-PS improved the DC breakdown strength with the maximum value of 408.9 kV/mm was obtained. This may attribute to excellent interface structure formed between PP matrix and PS particles. 相似文献