A drawn high density polyethylene(HDPE)has been measured by Raman spectroscopy and differential scanning calorimetry (DSC). The crystalline structure of drawn HDPE is analysed by the Raman internal modes in terms of mass fractions of the crystalline orthorhombic phase, the liquid- like amorphous phase and the disordered anisotropic phase. The mass fractions depend on draw temperature T_d and draw ratio R_d . The fraction of disordered anisotropic amorphous phase changes very little with, the T_d and increases with increasing R_d. Sum of the mass fractions of crystalline orthorhombic phase and the disordered anisotropic phase increases linearly as the same slope as the crystallinity W_c determined from DSC measurements with increasing T_d or R_d and it is higher than the W_c for all the samples. The results show that the mass fraction of disordered anisotropic phase is partially devoted by the taut tie molecules (TTM s) in the amorphous state. The dependence of the disordered anisotropic phase on T_d and R_d supports the mechanism of plastic deformation of fibre structure. 相似文献
The correlation between Young's modulus of mica-filled high density polyethylene (HDPE), low density polyethylene(LDPE) and the state of dispersion of plasma-treated mica in the polymer matrices was studied. The modulus and the number average diameter of mica aggregates in matrix were determined with tensile testing and image analysis respectively. The interface structure of the filler/matrix and the bulk structure of matrix were examined through the dielectric spectrometry, differential scanning calorimetry (DSC) and dynamic viscoelastic spectrometry. The results show that the Young's modulus of the filial polyethylene depends to a great extent upon the state of dispersion of filler in matrix, but it is independent of the interface structure and bulk structure. The better the dispersion, the higher the Young's modulus. 相似文献
The phase diagram of a ternary system of PVDF,dibutyl phthalate (DBP) and di(2-ethylhexyl) phthalate (DEHP) was determined in terms of a pseudo binary system with the same polymer concentration and different DBP content in diluent mixture.The experimental results showed that as the DBP content increased in diluent mixture,the phase separation changed from liquid-liquid phase separation to solid-liquid phase separation,and both the cloudy point for L-L phase separation and crystallization temperature shif... 相似文献
In this paper, we theoretically show that the field-free molecular alignment can be controlled by shaping the femtosecond laser pulse with a periodic phase step modulation, involving the maximum degree and temporal structure of the molecular alignment. We show that the molecular alignment can be completely suppressed or reconstructed as that by the transform-limited laser pulse, the temporal structure of the alignment transient can be controlled with a desired shape, and the molecular alignment and antialignment for any temporal structure can be switched. Furthermore, we also show that both the degree and direction of the molecular alignment at a fix time delay can be continuously modulated. 相似文献
A novel and a simple method that allows direct imaging of viscous samples by cryo-TEM (cryo-transmission electron microscopy) is presented. A fracture on the vitrified sample is created in a controlled way. In the fracture, some edges are thin enough to allow direct imaging in transmission mode. The method was used to directly image a nonionic surfactant lamellar phase where a random mesh structure is formed at lower temperatures (<10 degrees C). A so-called random mesh phase, characterized by the presence of perforated surfactant bilayers, is imaged here for the first time. Images from the mesh structure are compared with images from the classical lamellar structure formed at room temperature. 相似文献
Summary: A mixture of poly(vinyl methyl ether) (PVME) and a polystyrene derivative bearing cinnamate groups (PSC) was chemically designed so that its phase separation can be tunable by visible light for computer‐assisted irradiation (CAI) experiments. This PSC/PVME blend exhibits a lower critical solution temperature (LCST) and undergoes phase separation upon irradiation with 405 nm visible light. The phase separation was induced by photodimerization of the cinnamate moieties in the presence of 5‐nitroacenaphthene used as a photosensitizer. It was found that for visible light with high intensity, phase separation process was almost frozen by photodimerization of the cinnamate groups which act as a photo‐cross‐linker for the PSC component. It is demonstrated in this work that by using this PSC/PVME blend, phase separation restricted to the micrometer scales can be induced and manipulated by irradiation using a computer‐controlled digital projector. These preliminary results open a new route for spatio‐temporal manipulation of phase separation in photo‐reactive polymer blends.
Computer‐assisted irradiation method for a polymer blend with phase separation drivable by visible light. 相似文献
