Characterization
Reza Poorghasemi; Yousef Jahani
Abstract
In this work, the compatibility and crystallinity of low density polyethylene (LDPE) and polybutene-1 (PB-1) blends were studied. Various blends of LDPE/PB-1 containing 5, 10 and 20 wt.% PB-1 were prepared in a corotating twin-screw extruder and characterized by scanning electron microscopy (SEM), shear ...
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In this work, the compatibility and crystallinity of low density polyethylene (LDPE) and polybutene-1 (PB-1) blends were studied. Various blends of LDPE/PB-1 containing 5, 10 and 20 wt.% PB-1 were prepared in a corotating twin-screw extruder and characterized by scanning electron microscopy (SEM), shear oscillation rheology and wide-angle X-ray diffractometry (WAXD). A matrix-droplet morphology was observed in SEM images, indicating incompatibility of the two polymers in the solid state. Compared to neat LDPE, the relaxation spectra of the blends were broadened, and a slight increase in their relaxation times was observed. The relaxation time of the blends was enhanced by increasing PB-1 content, which was further proved by fitting rheological data in the Carreau-Yasuda model. Deviation of Cole-Cole diagrams from circular shape means that the blend samples were not miscible and the positive-deviation behavior of the complex viscosity and storage modulus from the mixing rule revealed the formation of strong interfacial interactions. The crystallinity of both LLDPE and PB-1 was decreased as a result of blending. The peaks attributed to the form II of PB-1 crystals were eliminated and the peaks related to LDPE were obviously weakened, suggesting to prevent crystallinity of polymers which is associated with a reduction in the total crystallinity percentage for the blend. The reduction of crystallinity was more pronounced in PB-1 phase.
Polyolefin degradation
Soheyl Khajehpour-Tadavani; Gholam-Reza Nejabat; Mohammad-Mahdi Mortazavi
Abstract
Crystallinities of high-density polyethylene (HDPE) films containing various amounts of an oxo-biodegradable additive (HES-W) were investigated immediately after preparation and 6 weeks after ultraviolet (UV) irradiation (λ=254 nm). HDPE granules were mixed with oxo-biodegradable masterbatch in ...
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Crystallinities of high-density polyethylene (HDPE) films containing various amounts of an oxo-biodegradable additive (HES-W) were investigated immediately after preparation and 6 weeks after ultraviolet (UV) irradiation (λ=254 nm). HDPE granules were mixed with oxo-biodegradable masterbatch in a twin-screw extruder and the extrudates were converted into films with thicknesses of 35±5 micrometers. The films were exposed to UV light for 6 weeks. Crystallinities of the films are investigated by X-ray diffraction spectroscopy (XRD) and differential scanning calorimetry (DSC). The XRD results show that upon UV exposure, the crystallinities of the films enhance. The DSC thermograms have confirmed the XRD results and also show a decrease in melting points of the samples after UV exposure. Further investigations on viscosity average molecular weights (Mv) of the samples show that their Mv decrease sharply after UV exposure. Scanning electron microscopy (SEM) shows clear cracks on the samples surfaces after 6 weeks exposure to UV irradiation. Investigating the functionalities of the polymers through Fourier transform infrared spectroscopy (FTIR) show the emergence of carbonyl peaks after UV irradiation so that the carbonyl index of the samples increases. It is concluded that maximum oxo-biodegradation enhancement of the HDPE film samples can be achieved by using a specific amount of the oxo-compound (3 wt%); furthermore the crystallinities of the samples show considerable enhancement after UV exposure which can be due to better packing ability of low molecular weight chains along with probable dipole-dipole attractions between the carbonyl groups on different newly formed short polar chains.
Structure and property relationship
Majid Habibollahi; Morteza Ehsani; Jalil Morshedian
Abstract
In this study, poly carbonate (PC) and poly (ethylene terephthalate) (PET) were reactive melt-blended under two different conditions to produce PC/PET copolymers. For each condition, samples were taken at specified mixing times representative a specific structure of copolymers and each one employed to ...
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In this study, poly carbonate (PC) and poly (ethylene terephthalate) (PET) were reactive melt-blended under two different conditions to produce PC/PET copolymers. For each condition, samples were taken at specified mixing times representative a specific structure of copolymers and each one employed to physically compatibilize a PC/PET blend with a fixed composition. Reactive blending and copolymer structure are described by solubility analysis results. Continues declining and going through a minimum are two trends of solubility versus mixing time depending on reactive blending condition. Decreasing and increasing patterns of solubility curves were attributed to the formation of copolymers with longer and shorter block lengths, respectively, and the level of solubility was related to the amount of produced copolymers. Differential scanning calorimetry (DSC) and scanning electron microscopy (SEM) techniques were employed to investigate blend compatibility. The content and structure of copolymers showed favorable correlation of Tg differences of blend components and PET crystallinity. As expected, Tg of blend components approached to each other by the addition of copolymers, and the copolymers with longer block length caused less Tg differences. The melting point and crystallinity of PET were affected by introducing the copolymers too. In addition to the main melting endotherm, melting endotherm peaks of compatibilized blends had a shoulder that its corresponding melting point and crystallinity are related to the copolymer structure so that the longer length of block copolymer or higher its amount leads to the higher melting points. The SEM micrographs showed that, after the addition of the copolymer, smaller PET particles formed and uniformly dispersed in the PC matrix. A strong correlation between the blend morphology and the level of blend compatibility was demonstrated. The more compatibilized PC/PET blend, the better dispersion of PET particles in the PC matrix was obtained. The results of this study could be a basis for designing and production of compatibilizers suitable to achieve a desired level of compatibility in PC and polyester blends, specially in PC/PET blend.
Structure and property relationship
Ali Yadegari; Jalil Morshedian; Hossein-Ali Khonakdar; Udo Wagenknecht
Abstract
High density polyethylene (HDPE) films were produced using cast film extrusion process with different draw ratios, ranging from 16.9 to 148.8. Morphology, crystallinty and orientation state of crystalline and amorphous phases of the cast films were investigated using scanning electron microscopy (SEM), ...
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High density polyethylene (HDPE) films were produced using cast film extrusion process with different draw ratios, ranging from 16.9 to 148.8. Morphology, crystallinty and orientation state of crystalline and amorphous phases of the cast films were investigated using scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and polarized Fourier transform infrared spectroscopy (FTIR) analyses, respectively. The anisotropic crystalline structures of row-nucleated lamellar morphology were observed for the films produced with high draw ratios. The crystalline phase axes orientation functions were found to be significantly dependent on the applied draw ratios. As expected, annealing increased the crystallinity and melting point temperature (Tm) of the cast films and on the other hand, it also enhanced the crystalline phase orientation. However, the results revealed that annealing also promoted non-twisted lamellar structures, since it increased fc values (c-axis orientation function) and decreased fa values (a-axis orientation function) simultaneously. Additionally, it was found that the annealing induced enhancement in c-axis orientation function was more significant for the cast films with lower draw ratios, therefore, it was dependent on the draw ratio.
