The condensed behavior of polymer fluids were studied based on the van der Waals interaction. By comparing the phase diagram of pure polymer fluids and that of van der Waals non-ideal fluids, it is found that (1) pure polymer fluids show a similar phase diagram to van der Waals non-ideal fluids; (2) the differences between the phase diagrams were caused by the difference of chain lengths. It is explained that why the vapor pressure of polymer is hard to detect and why the negative pressure can exist in polymer liquids. It is also found that some scaling relations exist between the reduced critical pressure and the chain length, and the reduced critical volume and the chain length.
The isothermal and non-isothermal crystallization kinetics of LCBPP and linear-iPP was investigated by optical microscopy and differential scanning calorimetry (DSC). The optical microscopy results in the isothermal crystallization process show that the crystals of LCBPP grow slower than the crystals of the linear-iPP. This originates from the low chain mobility, or in other words, the lower chain diffusion rate of LCBPP due to the existence of long side chains. The DSC results in the isothermal crystallization process show that the LCBPP exhibits, however, a higher overall crystallization rate with respect to the linear-iPP. This is related to the higher nucleation ability of LCBPP since the isothermal crystallization process of both LCBPP and linear-iPP are nucleation-dominated. Avrami analysis indicates that the nucleation nature and crystal growth manner of LCBPP and linear-iPP are about the same. The analy- ses of the non-isothermal crystallization processes indicate an increment in crystallization rate with increasing cooling rate. But at any cooling rate, the linear-iPP crystallizes more quickly than the LCBPP. This implies that the non-isothermal crystallization processes of LCBPP and linear-iPP are diffu- sion-dominated, in which the lower chain diffusion rate of LCBPP results in the slower crystallization of it.
Hyperbranched polymer-cored star polyfluorenes with high molecular weights and narrow molecular weight distribution were prepared by palladium-catalyzed one-pot Suzuki polycondensation of multi- functional cores and an AB-type monomer. The optical, electrochemical and thermal properties of the hyperbranched polymer-cored star polymers were investigated. These polymers exhibited good ther- mal and color stability in solid state, and there was no significant blue-green emission after the poly- mers had been annealed in air for 2.5 h. Their three-dimensional hyperbranched structures could ef- fectively reduce the aggregation of the peripheral rigid linear conjugated polyfluorene chains.
Crystallization behavior and resultant crystalline structure of a series of temperature-rising elu-tion-fractionated specimen of a Ziegler-Natta catalyst-synthesized propylene-ethylene random co-polymer were studied by DSC, WAXD and AFM. The experimental results indicate that both crystalliza-tion temperature and propylene sequence length exhibit great influence on the crystallization behavior and crystalline structure of the copolymer. It was found that the ethylene co-monomers acting as point defects inserted into the polypropylene chains play an important role in the formation of γ-iPP. As the co-monomer content increases, the crystallizable sequence length of iPP decreases, which produces an appropriate condition for its γ crystallization. At the same time, the existence of chain defects leads to a lower crystallinity of the copolymer and imperfection of the resultant crystals. For each individual sample with certain propylene sequence length or ethylene content, the increment of γ-iPP crystal content with increasing crystallization temperature demonstrates that higher crystallization tempera-ture is in favor of the γ-iPP crystallization. Pure γ-iPP crystals have been got in samples with propylene sequence length lower than 21 under suitable crystallization conditions.
Inspired by the locomotion of terrestrial limbless animals, the present work attempt to study the motion of biomimetic system based on poly（vinyl alcohol） / dimethylsulfoxide gel. The system was operated in air by employing a non-contacted DC electric field. The results showed that the gel exhibited a long-range snail-like motion and had a very fast response rate.
