The effects of ultrasonic oscillations on properties and structure of extruded highdensity polyethylene (HDPE) were studied. The experimental results show that ultrasonic oscillations can improve the surface appearance of the HDPE extrudates; increase the productivity of the HDPE extrudates; and decrease the die pressure, melt viscosity, and flow activation energy of the HDPE. The processing properties of the HDPE improve greatly in the presence of ultrasonic oscillations. Linear viscoelastic properties tests show that dynamic shear viscosity and zero shear viscosity decrease in the presence of ultrasonic oscillations. Ultrasonic oscillations can improve crystal perfection and thermal stability of HDPE. At appropriate ultrasound intensity, ultrasonic scillations could also increase the mechanical strength of extruded HDPE. The gel permeation chromatography (GPC) results show that at high ultrasound intensity and low rotation speed of extrusion, ultrasonic oscillations causes chain scission of HDPE, which result in a decrease of molecular weight and an increase of melt flow index.

The ultrasonic degradation of polyamide 6 (PA6) melt was conducted in a specially designed reactor. The effects of initial molecular weight of PA6, irradiation time, ultrasonic intensity as well as ultrasonic irradiation distance on the ultrasonic degradation of PA6 melt were investigated. Some surprising experimental results show that for low molecular weight PA6 (LPA6), the viscosity-average molecular weight of LPA6 increases in the presence of ultrasonic oscillations due to extension reaction of end groups (eCOOH and eNH2), while for high molecular weight PA6 (HPA6), the viscosity-average molecular weight of HPA6 decreases with irradiation time, and passes through a minimum, then increases with irradiation time, up to a limiting molecular weight. Ultrasonic degradation kinetics of HPA6 melt obey the equation: Mt% MNCAe kt: FTIR analysis and a microtitration method confirm that the chain scission of HPA6 under ultrasonic irradiation occurs at CeN bonds. A plausible ultrasonic degradation model of the polymer melt based on molecular movement is proposed. Published by Elsevier Ltd.

Three kinds of polymer/layered nanocomposites were prepared via ultrasonic extrusion. Experimental results showed that ultrasonic oscillations could mostly decrease the size and its distribution of clay particles in polymer matrix. Therefore, crystal size of polymer matrix decreases. For PA6-based nanocomposites with higher compatibility, the ultrasonic oscillations can also affect the microstructure of clay, causing more regions of exfoliated clay. Due to better dispersion of clay and smaller crystal size, the elongation at break of polymer/layered nanocomposites ultrasonically treated got greatly increased, meanwhile ultrasonic oscillations also improved their other mechanical properties, such as tensile and impact strength.

In this paper, high power ultrasound was introduced into polystyrene (PS)/ethylene-propylene diene monomer (EPDM)(80/20) blend melts during extrusion. The structure and properties of PS/EPDM blends treated ultrasonically, such as their mechanical properties, phasemorphology, dynamic rheological behavior and the size distribution fractal dimension of dispersed particles, as well as the interfacial tension between the PS and EPDMphases, were studied. The experimental results indicated that ultrasonic treatment could improve the compatibility of PS/EPDM blends. This is attributed to the formation of a copolymer of PS and EPDMby the combination of different macroradicals, resulting from the homolytic cleavage of polymer chains induced by ultrasonic irradiation. The disproportional termination of the macroradicals leads to the degradation of PS and EPDM. Some properties, like mechanical and linear viscoelastic characteristics, were affected by both ultrasonic compatibilization and degradation. These properties depended strongly on the ultrasonic intensity, ultrasonic treatment time and number of extrusions (repeated extruded times). Differential particle size distribution of the dispersed phase in PS/EPDM blends.

In this paper, the effect of ultrasonic intensity on the degradation of high-density polyethylene (HDPE) melt, degradation mechanism, ultrasonic degradation kinetics of HDPE melt as well as the development of molecular weight distribution of HDPE melt during ultrasonic degradation were studied. In the initial stage, the ultrasonic degradation of HDPE melt shows a random scission process, and the molecular weight distribution broadens. After that, the ultrasonic degradation of HDPE melt shows a nonrandom scission process, and the molecular weight distribution of HDPE melt narrows with ultrasonic irradiation time. The average molecular weight of HDPE decreases with the increase of ultrasonic intensity and increases and trends forward that of undegraded HDPE with the increase of distance from ultrasonic probe tip, indicating that attenuation of ultrasonic intensity in HDPE melt is very quick. Ultrasonic degradation kinetics of HDPE melt obeys the equation: Mt