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High-density Polyethylene (high-density + polyethylene)
Selected AbstractsHigh-density polyethylene (HDPE)-degrading potential bacteria from marine ecosystem of Gulf of Mannar, IndiaLETTERS IN APPLIED MICROBIOLOGY, Issue 2 2010V. Balasubramanian Abstract Aims:, Assessment of high-density polyethylene (HDPE)-degrading bacteria isolated from plastic waste dumpsites of Gulf of Mannar. Methods and Results:, Rationally, 15 bacteria (GMB1-GMB15) were isolated by enrichment technique. GMB5 and GMB7 were selected for further studies based on their efficiency to degrade the HDPE and identified as Arthrobacter sp. and Pseudomonas sp., respectively. Assessed weight loss of HDPE after 30 days of incubation was nearly 12% for Arthrobacter sp. and 15% for Pseudomonas sp. The bacterial adhesion to hydrocarbon (BATH) assay showed that the cell surface hydrophobicity of Pseudomonas sp. was higher than Arthrobacter sp. Both fluorescein diacetate hydrolysis and protein content of the biofilm were used to test the viability and protein density of the biomass. Acute peak elevation was observed between 2 and 5 days of inoculation for both bacteria. Fourier transform infrared (FT-IR) spectrum showed that keto carbonyl bond index (KCBI), Ester carbonyl bond index (ECBI) and Vinyl bond index (VBI) were increased indicating changes in functional group(s) and/or side chain modification confirming the biodegradation. Conclusion:, The results pose us to suggest that both Pseudomonas sp. and Arthrobacter sp. were proven efficient to degrade HDPE, albeit the former was more efficacious, yet the ability of latter cannot be neglected. Significance and Impact of the Study:, Recent alarm on ecological threats to marine system is dumping plastic waste in the marine ecosystem and coastal arena by anthropogenic activity. In maintenance phase of the plastic-derived polyethylene waste, the microbial degradation plays a major role; the information accomplished in this work will be the initiating point for the degradation of polyethylene by indigenous bacterial population in the marine ecosystem and provides a novel eco-friendly solution in eco-management. [source] Ultrasound aided extrusion process for preparation of polyolefin,clay nanocompositesPOLYMER ENGINEERING & SCIENCE, Issue 8 2008Sergey Lapshin A continuous ultrasound assisted process using a single screw compounding extruder with an ultrasonic attachment was developed to prepare polyolefin/clay nanocomposites. High-density polyethylene and isotactic polypropylene were compared. The feed rate that controls the residence time of the polymer in the ultrasonic treatment zone was varied. Die pressure and power consumption were measured. Rheological properties, morphology, and mechanical properties of the untreated and ultrasonically treated nanocomposites were studied. Similarities and differences of obtained nanocomposites are discussed based on their properties and structural characteristics. The modified Halpin-Tsai theory of composite materials has been employed in order to predict the effect of incomplete exfoliation of clay platelets on the Young's modulus of the nanocomposites. A good agreement between experimental and theoretical data has been observed when reduction of the reinforcement efficiency of clay had been incorporated through the reduced aspect ratio of elementary clay platelets. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Multiaxial fatigue criterion for a high-density polyethylene thermoplasticFATIGUE & FRACTURE OF ENGINEERING MATERIALS AND STRUCTURES, Issue 6 2010A. BERREHILI ABSTRACT The multiaxial fatigue behaviour of a high-density polyethylene was investigated at room temperature and constant frequency. As a consequence of the mode of failure, an end-of-life criterion for fatigue tests is discussed in the first part of the work, in order to define the number of cycles to failure. Based on force controlled fatigue tests under tension, compression and torsion at two stress ratio, a multiaxial fatigue criterion including the stress-ratio effect is proposed for the fatigue design of this polymer. This criterion is based on the maximum and mean values of the second invariant of the stress tensor. [source] On the high-density polyethylene extrusion: Numerical, analytical and experimental modelingADVANCES IN POLYMER TECHNOLOGY, Issue 3 2010A. G. Mamalis Abstract A three-dimensional numerical model was developed to investigate the nonisothermal, non-Newtonian polymer flow through a cone cylindrical die used in the HDPE (high-density polyethylene) extrusion process. The numerical model was based on the computational fluid dynamics code COMSOL 3.4 the finite element method, and it was used to calculate pressure, flow, and temperature distributions in a cone cylindrical die used for industrial-scale extrusion of an HDPE rod. The model also accounted for viscous heating. In addition, pressure and temperature data were derived using an analytical solution. The numerical approach agrees fairly well with the experimental data recorded during the extrusion process of the material. © 2010 Wiley Periodicals, Inc. Adv Polym Techn 29:173,184, 2010; View this article online at wileyonlinelibrary. DOI 10.1002/adv.20185 [source] Effect of EVA as compatibilizer on the mechanical properties, permeability characteristics, lamellae orientation, and long period of blown films of HDPE/clay nanocompositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010Juliano Marini Abstract Two ethylene-vinyl acetate (EVA) resins with 19% (EVA19) and 28% (EVA28) of vinyl groups were used as compatibilizers for nanocomposites of high-density polyethylene (HDPE) and nanoclays. Two nanoclays were also used, one with a nonpolar surfactant (C15A) and another with a polar surfactant (C30B). The HDPE/EVA19/C15A formed an intercalated structure, while the HDPE/EVA28/C30B had surfactant loss. Blown films of these compositions were produced. A two-phase morphology made of HDPE and EVA/nanoclay particles was observed, which was responsible for the increase in water vapor and oxygen permeability rates of the films. The elastic modulus E along the transverse direction of the films was higher than along the machine direction due to preserved orientation given by the spiral die; the lamellae orientation was measured by small-angle X-rays diffraction. The highest E was observed in the HDPE/EVA19/C15A film due to stronger interactions. The long period of the HDPE lamellas was not affected by the presence of the EVA and nanoclay. A model was proposed to explain the improvement in elastic modulus due to the processing conditions and components' interactions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Rheology behavior of high-density polyethylene/diluent blends and fabrication of hollow-fiber membranes via thermally induced phase separationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2010Jianli Wang Abstract The phase-separation behavior of high-density polyethylene (HDPE)/diluent blends was monitored with a torque variation method (TVM). The torque variation of the molten blends was recorded with a rheometer. It was verified that TVM is an efficient way to detect the thermal phase behavior of a polymer,diluent system. Subsequently, polyethylene hollow-fiber membranes were fabricated from HDPE/dodecanol/soybean oil blends via thermally induced phase separation. Hollow-fiber membranes with a dense outer surface of spherulites were observed. Furthermore, the effects of the spinning temperature, air-gap distance, cold drawing, and HDPE content on the morphology and gas permeability of the resultant membranes were examined. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Crystallization and melting behavior of HDPE in HDPE/teak wood flour composites and their correlation with mechanical propertiesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2010Kamini Sewda Abstract The nonisothermal crystallization behavior and melting characteristics of high-density polyethylene (HDPE) in HDPE/teak wood flour (TWF) composites have been studied by differential scanning calorimetry (DSC) and wide angle X-ray diffraction (WAXD) methods. Composite formulations of HDPE/TWF were prepared by varying the volume fraction (,f) of TWF (filler) from 0 to 0.32. Various crystallization parameters evaluated from the DSC exotherms were used to study the nonisothermal crystallization behavior. The melting temperature (Tm) and crystallization temperature (Tp) of the composites were slightly higher than those of the neat HDPE. The enthalpy of melting and crystallization (%) decrease with increase in the filler content. Because the nonpolar polymer HDPE and polar TWF are incompatible, to enhance the phase interaction maleic anhydride grafted HDPE (HDPE-g-MAH) was used as a coupling agent. A shift in the crystallization and melting peak temperatures toward the higher temperature side and broadening of the crystallization peak (increased crystallite size distribution) were observed whereas crystallinity of HDPE declines with increase in ,f in both DSC and WAXD. Linear correlations were obtained between crystallization parameters and tensile and impact strength. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Photografting of acrylic acid and methacrylic acid onto polyolefines initiated by formaldehyde in aqueous solutionsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2009Jianmei Han Abstract Formaldehyde aqueous solution can act as an effective photoinitiating system for water-borne photografting. The photografting of acrylic acid (AA) and methacrylic acid (MAA) onto high-density polyethylene (HDPE), low-density polyethylene (LDPE) and polypropylene (PP) initiated by formaldehyde aqueous solutions has been reported. The effects of formaldehyde content and monomer concentration on grafting varied with the polymeric substrates and monomers used. For the grafting of AA onto HDPE, the extent of grafting increased with increasing formaldehyde content in the solution, monomer concentration had a little effect on grafting. Whereas for the grafting of MAA onto HDPE, the grafting performed in 8% formaldehyde aqueous solution lead to the highest extent of grafting, the extent of grafting increased with monomer concentration till 2.5 mol/L. MAA was easier to be grafted onto the polyolefins than AA. The easiness of grafting occurring on the polyolefins was in a decreasing order of LDPE > HDPE > PP. Qualitative and semi-quantitative Fourier transform infrared (FTIR) characterizations of the grafted samples were performed. For both grafted LDPE and PP samples, at the same irradiation time, the carbonyl index of the samples grafted with MAA was higher than that grafted with AA. The FTIR results are in accord with the results obtained by gravimetric method. The water absorbency of the grafted samples increased almost linearly with the extent of grafting. The PE films grafted with AA adsorbed more water than those grafted with MAA. This study had broadened the water-borne initiating system for photografting. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Influence of compatibilizer on notched impact strength and fractography of HDPE,organoclay compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2009Waraporn Rattanawijan Abstract The focus of this study was the notched impact property of high-density polyethylene (HDPE),organoclay composites and the resultant morphology of impact-fractured surfaces. Composites with a different organoclay content and degree of organoclay dispersion were compared with neat HDPE under identical conditions. The degree of organoclay dispersion was controlled through the use of a compatibilizer, maleic anhydride grafted polyethylene. It was found that the addition of organoclay can slightly increase the elastic modulus and notched impact strength of the composite. When the level of organoclay dispersion was improved by using compatibilizer, elastic modulus and toughness further increased. A significant increase in yield strength was also notable. The presence of organoclay was found to suppress strain hardening of the matrix during tensile testing. The impact-fractured surfaces of failed specimens were studied with scanning electron microscopy. The micromechanism for the increased toughness of HDPE,organoclay composites was discussed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Simultaneous measurement of resistance and viscoelastic responses of carbon black-filled high-density polyethylene subjected to dynamic torsionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008Jianfeng Zhou Abstract The conduction and viscoelastic responses to temperature are measured simultaneously for carbon black (CB) filled high-density polyethylene (HDPE) subjected to dynamic torsion. PTC/NTC transition was correlated with the loss tangent peak and the quasi modulus plateau, which was ascribed to the filler network. The bond-bending model of elastic percolation networks was used to reveal the structural mechanisms for the cyclic resistance changes at different temperatures. The resistance changes at lower temperatures depended on the deformation of the polymer matrix, while the changes in melting state were mainly attributed to the rearrangement of the CB network. A simple scaling law is derived to relate resistance and dynamic storage modulus in the melting region. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Morphologies and mechanical properties of HDPE induced by small amount of high-molecular-weight polyolefin and shear stress produced by dynamic packing injection moldingJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008Zhanchun Chen Abstract To better understand the effect of a small amount of high-molecular-weight polyethylene (HMWPE) on the mechanical properties and crystal morphology under the shear stress field, the dynamic packing injection molding (DPIM) was used to prepare the oriented pure polyethylene and its blends with 4% HMWPE. The experiment substantiated that the further improvement of tensile strength along the flow direction (MD) of high-density polyethylene (HDPE)/HMWPE samples was achieved, whereas the tensile strength along the transverse direction (TD) still substantially exceeded that of conventional molding. Tensile strength in both flow and TDs were highly enhanced, with improvements from 23 to 76 MPa in MD and from 23 to 31 MPa in TD, besides the toughness was highly improved. So, the samples of HDPE/HMWPE transformed from high strength and brittleness to high strength and toughness. The obtained samples were characterized via SEM and TEM. For HDPE/HMWPE, the lamellae of the one shish-kebab in the oriented region may be stretched into other shish-kebab structures, and one lamella enjoys two shish or even more. This unique crystal morphology could lead to no yielding and necking phenomena in the stress,strain curves of HDPE/HMWPE samples by DPIM. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Toughening of recycled polystyrene used for TV backsetJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Xiaoting Fu Abstract The recycled polystyrene (rPS) was toughened with ethylene-octylene copolymer thermoplastic elastomer (POE) and high-density polyethylene (HDPE) with various melt flow index (MFI), compatibilized by styrene-butadiene-styrene copolymer (SBS) to enhance the toughness of rPS for use as TV backset. The rPS/POE binary blends exhibited an increased impact strength with 5,10 wt % POE content followed by a decrease with the POE content up to 20 wt %, which could be due to poor compatibility between POE and rPS. For rPS/POE/SBS ternary blends with 20 wt % of POE content, the impact strength increased dramatically and a sharp brittle-ductile transition was observed as the SBS content was around 3,5 wt %. Rheological study indicated a possible formation of network structure by adding of SBS, which could be a new mechanism for rPS toughening. In rPS/POE/HDPE/SBS (70/20/5/5) quaternary blends, a fibril-like structure was observed as the molecular weight of HDPE was higher (with lower MFI). The presence of HDPE fibers in the blends could not enhance the network structure, but could stop the crack propagation during fracture process, resulting in a further increase of the toughness. The prepared quaternary blend showed an impact strength of 9.3 kJ/m2 and a tensile strength of 25 MPa, which can be well used for TV backset to substitute HIPS because this system is economical and environmental friendly. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Amorphous orientation and its relationship to processing stages of blended polypropylene/polyethylene fibersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Amy M. Trottier Abstract Changes in the molecular orientation, melting behavior, and percent crystallinity of the individual components in a fibrous blend of isotactic polypropylene (iPP) and high-density polyethylene (HDPE) that occur during the melt extrusion process were examined using wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). The crystalline orientation of each component was found using Wilchinsky's treatment of uniaxial orientation and described by the Hermans,Stein orientation parameter. The amorphous orientation was found by resolving the X-ray diffraction pattern in steps of the azimuthal angle into its iPP and HDPE crystalline and amorphous reflections. The utility of DSC and WAXD analyses to capture the effects of small differences in processing, and the use of these results as fingerprints of a particular manufacturing process were demonstrated. Major increases in the melting temperatures, percent crystallinities, and molecular orientations of the iPP and HDPE components occurred during the main stretching stage of the melt extrusion process. The annealing stage was found to have little to no effect on the melting behavior and molecular orientation of these components. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Effect of morphology on the electric conductivity of binary polymer blends filled with carbon blackJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007Zhongbin Xu Abstract Several carbon black (CB)-filled binary polymer blends were prepared in Haake rheometer. Distribution states of CB and effect of morphology on the electric conductivity of different ternary composites were investigated. Under our experimental condition CB particles located preferentially at the interface between polymethyl methacrylate (PMMA) and polypropylene (PP) in PMMA/PP/CB composites, in high-density polyethylene (HDPE) phase in PP/HDPE/CB composites, and in Nylon6 (PA6) phase in polystyrene (PS)/PA6/CB, PP/PA6/CB, PMMA/PA6/CB, and polyacrylonitrile (PAN)/PA6/CB composites; the ternary composites in which CB particles locate at the interface of two polymer components have the highest electric conductivity when the mass ratio of the two polymers is near to 1 : 1. The ternary composites in which CB particles located preferentially in one polymer have the highest electric conductivity usually when the amount of the polymer component having CB particles is comparatively less than the amount of the polymer component not having CB particles; if the formulations of PS/PA6/CB, PP/PA6/CB, and PMMA/PA6/CB composites equaled and PA6/CB in them is in dispersed phase, PS/PA6/CB composites have the highest electric conductivity and PP/PA6/CB composites have the lowest electric conductivity; suitable amount of PS or PAN in PA6/CB composites increase the electric conductivity due in the formation of a parallel electrocircuit for electrons to transmit. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Dispersion of graphite nanosheets in polymer resins via masterbatch techniqueJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Guohua Chen Abstract The dispersion of graphite nanosheets (GNs) in polymer matrices via the masterbatch technique was investigated. Modifying resin was added to GNs to prepare blend which is designated as the masterbatch. Such masterbatches, containing 70,80 wt % of GN filler, were blended with target polymers via melt extrusion process to prepare polymer/GN nanocomposites. The extruded nanocomposites showed characteristic conducting percolation behaviors with the percolation thresholds mainly dependent on the miscibility of the modifying resin with polymer matrix. The percolation thresholds of AS (Acrylonitrile-Styrene compolymer)/GN and high-density polyethylene (HDPE)/GN nanocomposites prepared by this technique were about 9 and 14 wt % of GN, respectively. Scanning electron microscopy and other characterizations showed that the GNs were well dispersed in AS and HDPE resins. The extrusion process and compatibility of the modifying resin with target polymer proved to be important factors for the homogeneity of the nanodispersion. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3470,3475, 2007 [source] Dynamic mechanical properties and morphology of high-density polyethylene/CaCO3 blends with and without an impact modifierJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Yu-Lin Yang Abstract Dynamic mechanical analysis and differential scanning calorimetry were used to investigate the relaxations and crystallization of high-density polyethylene (HDPE) reinforced with calcium carbonate (CaCO3) particles and an elastomer. Five series of blends were designed and manufactured, including one series of binary blends composed of HDPE and amino acid treated CaCO3 and four series of ternary blends composed of HDPE, treated or untreated CaCO3, and a polyolefin elastomer [poly(ethylene- co -octene) (POE)] grafted with maleic anhydride. The analysis of the tan , diagrams indicated that the ternary blends exhibited phase separation. The modulus increased significantly with the CaCO3 content, and the glass-transition temperature of POE was the leading parameter that controlled the mechanical properties of the ternary blends. The dynamic mechanical properties and crystallization of the blends were controlled by the synergistic effect of CaCO3 and maleic anhydride grafted POE, which was favored by the core,shell structure of the inclusions. The treatment of the CaCO3 filler had little influence on the mechanical properties and morphology. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3907,3914, 2007 [source] Thermal and mechanical properties of uncrosslinked and chemically crosslinked polyethylene/ethylene vinyl acetate copolymer blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2007H. A. Khonakdar Abstract Uncrosslinked and chemically crosslinked binary blends of low- and high-density polyethylene (PE), with ethylene vinyl acetate copolymer (EVA), were prepared by a melt-mixing process using 0,3 wt % tert -butyl cumyl peroxide (BCUP). The uncrosslinked blends revealed two distinct unchanged melting peaks corresponding to the individual components of the blends, but with a reduced overall degree of crystallinity. The crosslinking further reduced crystallinity, but enhanced compatibility between EVA and polyethylene, with LDPE being more compatible than HDPE. Blended with 20 wt % EVA, the EVA melting peak was almost disappeared after the addition of BCUP, and only the corresponding PE melting point was observed at a lowered temperature. But blended with 40% EVA, two peaks still existed with a slight shift toward lower temperatures. Changes of mechanical properties with blending ratio, crosslinking, and temperature had been dominated by the extent of crystallinity, crosslinking degree, and morphology of the blend. A good correlation was observed between elongation-at-break and morphological properties. The blends with higher level of compatibility showed less deviation from the additive rule of mixtures. The deviation became more pronounced for HDPE/EVA blends in the phase inversion region, while an opposite trend was observed for LDPE/EVA blends with co-continuous morphology. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3261,3270, 2007 [source] Low-Temperature Atomic Layer-Deposited TiO2 Films with Low PhotoactivityJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 3 2009Xinhua Liang Atomic layer deposition (ALD) has been successfully utilized for the conformal and uniform deposition of ultrathin titanium dioxide (TiO2) films on high-density polyethylene (HDPE) particles. The deposition was carried out by alternating reactions of titanium tetraisopropoxide and H2O2 (50 wt% in H2O) at 77°C in a fluidized bed reactor. X-ray photoelectron spectroscopy confirmed the deposition of TiO2 and scanning transmission electron microscopy showed the conformal TiO2 films deposited on polymer particle surfaces. The TiO2 ALD process yielded a growth rate of 0.15 nm/cycle at 77°C. The results of inductively coupled plasma atomic emission spectroscopy suggested that there was a nucleation period, which showed the reaction mechanism of TiO2 ALD on HDPE particles without chemical functional groups. TiO2 ALD films deposited at such a low temperature had an amorphous structure and showed a much weaker photoactivity intensity than common pigment-grade anatase TiO2 particles. [source] Effect of hindered piperidine light stabilizer molecular structure and UV absorber addition on the oxidation of HDPE.JOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 4 2004Part 2: Mechanistic aspects, electron spin resonance spectroscopy study, molecular modeling The first in this series of papers explored the effect of the structural characteristics of 2,2,6,6-tetramethylpiperidine-based hindered amine light stabilizers (HALS) on the thermal and photostabilization of high-density polyethylene. In the second part, the energies (stabilities) of the nitroxyl radicals and various intermediate species have been predicted using AccuModel® and related to stabilization performance and electron spin resonance (ESR) spectral data. Nitroxyl radicals with low predicted stability generally afforded improved thermal and photostabilization. ESR spectra were used to obtain values of nitroxyl radical concentration ([>NO·]) and g -factor as a function of pre-aging time for combinations of pre-aged HDPE and >NH HALS. Demethylation reactions of > N-methyl HALS resulted in uselessly weak ESR spectra. The HALS that afforded poor thermal oxidative stabilization gave rise to pronounced minima in [>NO·] that coincided with a maximum in hydroperoxide concentration. The g -factor values indicated that a predominant nitroxyl canonical form generally promoted superior thermal oxidative stabilization, whereas a predominance of the dipolar N·+O, form promoted superior photo-oxidative stabilization. These trends may be related to greater radical-scavenging and peroxide-trapping effects, respectively. Molecular modeling and ESR spectra can therefore provide valuable insight into the effectiveness of HALS and stabilization mechanisms. J. Vinyl Addit. Technol. 10:159,167, 2004. © 2004 Society of Plastics Engineers. [source] Additive interactions in the stabilization of film grade high-density polyethylene.JOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 2 2002Part I: Stabilization, influence of zinc stearate during melt processing The melt stabilization activity of some of the most commercially significant phenolic antioxidants and phosphites (alone and in combination), without and with zinc stearate, was studied in high-density polyethylene (HDPE) produced by Phillips catalyst technology. Multiple pass extrusion experiments were used to degrade the polymer melt progressively. The effect of stabilizers was assessed via melt flow rate (MFR) and yellowness index (YI) measurements conducted as a function of the number of passes. The level of the phenolic antioxidant remaining after each extrusion was determined by high-performance liquid chromatography (HPLC). Phenolic antioxidants and phosphites both improved the melt stability of the polymer in terms of elt viscosity retention; the influence of zinc stearate was found to be almost insignificant. However, phosphites and zinc stearate decreased the discoloration caused by the phenolic antioxidants. A correlation was found between the melt stabilization performance of phosphites and their hydroperoxide decomposition efficiency determind via a model hydroperoxide compound. Steric and electronic effects associated with the phosphorus atom influenced the reactivity towards hydroperoxides. Furthermore, high hydrolytic stability did not automatically result in lower efficiency. Besides phosphite molecular structure, stabilization activity was also influenced by the structure of the primary phenolic antioxidant and the presence of zinc stearate. [source] High-density polyethylene (HDPE)-degrading potential bacteria from marine ecosystem of Gulf of Mannar, IndiaLETTERS IN APPLIED MICROBIOLOGY, Issue 2 2010V. Balasubramanian Abstract Aims:, Assessment of high-density polyethylene (HDPE)-degrading bacteria isolated from plastic waste dumpsites of Gulf of Mannar. Methods and Results:, Rationally, 15 bacteria (GMB1-GMB15) were isolated by enrichment technique. GMB5 and GMB7 were selected for further studies based on their efficiency to degrade the HDPE and identified as Arthrobacter sp. and Pseudomonas sp., respectively. Assessed weight loss of HDPE after 30 days of incubation was nearly 12% for Arthrobacter sp. and 15% for Pseudomonas sp. The bacterial adhesion to hydrocarbon (BATH) assay showed that the cell surface hydrophobicity of Pseudomonas sp. was higher than Arthrobacter sp. Both fluorescein diacetate hydrolysis and protein content of the biofilm were used to test the viability and protein density of the biomass. Acute peak elevation was observed between 2 and 5 days of inoculation for both bacteria. Fourier transform infrared (FT-IR) spectrum showed that keto carbonyl bond index (KCBI), Ester carbonyl bond index (ECBI) and Vinyl bond index (VBI) were increased indicating changes in functional group(s) and/or side chain modification confirming the biodegradation. Conclusion:, The results pose us to suggest that both Pseudomonas sp. and Arthrobacter sp. were proven efficient to degrade HDPE, albeit the former was more efficacious, yet the ability of latter cannot be neglected. Significance and Impact of the Study:, Recent alarm on ecological threats to marine system is dumping plastic waste in the marine ecosystem and coastal arena by anthropogenic activity. In maintenance phase of the plastic-derived polyethylene waste, the microbial degradation plays a major role; the information accomplished in this work will be the initiating point for the degradation of polyethylene by indigenous bacterial population in the marine ecosystem and provides a novel eco-friendly solution in eco-management. [source] Aliphatic Ketones as Photoinitiators for PhotograftingMACROMOLECULAR RAPID COMMUNICATIONS, Issue 13 2004Huiliang Wang Abstract Summary: The photografting of methacrylic acid (MAA) onto high-density polyethylene (HDPE) initiated by butanone, pentan-3-one, and heptan-3-one is presented. These aliphatic ketones can act as photoinitiators for photografting when they are a component of a suitable solvent mixture with water and ethanol. It is possible that the photoinitiation effect of the aliphatic ketone is induced by the hydrogen bond formed between it and water. The grafting of 2 M MAA in different ketone/water/ethanol (30/30/40) solvents. [source] Quality of orange juice in barrier packaging materialPACKAGING TECHNOLOGY AND SCIENCE, Issue 5 2008C. Berlinet Abstract The vitamin C content and the colour of orange juice made from concentrate were measured during 9 months of storage at 20°C either under artificial light or in darkness. The packaging materials used were glass, standard monolayer polyethylene terephthalate (PET) and multilayer PET (PET/nylon and oxygen scavenger/PET) containers. In this experiment, all bottles were sealed with aluminium foil in order to avoid any cap effect. The results showed that in plastic packaging materials, the loss of vitamin C was related to the oxygen permeability, and that glass provided the best preservation of ascorbic acid. No statistical difference (p < 0.05) was revealed between the vitamin C content in the juice stored under artificial light or in darkness, whatever the packaging used. The modification of colour was studied with the L, a* and b* values during storage at 20°C under artificial light. L and b* decreased, revealing a reduction of lightness and yellow colour of the juice, whereas a* increased, due to the formation of brown pigments. This change in colour was partly related to the oxygen permeability of the packaging used. The losses of aroma compounds by permeation through the bottle (PET) and the cap (high-density polyethylene, HDPE) have also been investigated. The results showed that permeation mainly took place through the cap. The use of a multilayer cap [HDPE with internal barrier layer of low-density polyethylene (LDPE)/EvOH/LDPE] considerably limited the permeation of the aroma compounds studied, whatever the PET bottle used. Copyright © 2007 John Wiley & Sons, Ltd. [source] Packaging materials for fermented milk: effects of material crystallinity and polarity on food qualityPACKAGING TECHNOLOGY AND SCIENCE, Issue 3 2001S. E. A. Jansson Abstract The ability of a packaging material to protect the food product and extend its shelf-life depends on several material properties. In this work the effects of material crystallinity and polarity on the quality of fermented milk were studied. The fermented milk is a high-quality Swedish product, similar to yoghurt. The quality of the food product was determined as a function of storage time by containing the liquid in pouches of different materials. The material crystallinity was varied by using very low-density polyethylene, high-density polyethylene and aluminium laminate as packaging materials. Aluminium was used on account of its ,100%' gas-tightness. The polarity was varied by comparing an aliphatic polyketone with polyethylene of similar crystallinity. The carbon dioxide (CO2) and oxygen (O2) contents in the headspace of the pouches were determined. The food quality was determined by measuring whey syneresis, viscosity and the content of desired Bifidobacteria, as well as of undesired yeast and mould. A trained taste panel determined the degree of acidity and of the sparkling taste. It was found that the content of CO2 increased and that of O2 decreased in the pouches with increasing degree of crystallinity and increasing polarity. The sparkling taste of fermented milk was a clear function of the headspace CO2 content. The data presented here could thus be used to ,design' a package for a desired sparkling taste of the fermented milk by selecting a certain material crystallinity. Whey syneresis, viscosity and content of Bifidobacteria were found to be independent of pouch material. While the degree of whey syneresis and the viscosity increased with increasing storage time, the content of Bifidobacteria slowly decreased. The content of yeast and mould in the liquid was below the existing limit values for foodstuffs. The degrees of acidity and sparkling taste were highest for the liquids contained in aluminium and polyketone pouches, although the differences in acidulous taste between the various pouch materials were small. Copyright © 2001 John Wiley & Sons, Ltd. [source] Effects of reduced-rate methyl bromide applications under conventional and virtually impermeable plastic film in perennial crop field nurseriesPEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 8 2010Bradley D Hanson Abstract BACKGROUND: Producers of perennial crop nursery stock in California use preplant soil fumigation to meet state phytosanitary requirements. Although methyl bromide (MB) has been phased out in many agricultural industries, it is still the preferred treatment in the perennial nursery industry and is used under Critical Use Exemptions and Quarantine/Preshipment provisions of the Montreal Protocol. The present research was conducted to evaluate reduced-rate MB applications sealed with conventional and low-permeability plastic films compared with the primary alternative material. RESULTS: Reduced rates (100,260 kg ha,1) of MB applied in combination with chloropicrin (Pic) and sealed with a low-permeability plastic film provided weed and nematode control similar to the industry standard rate of 392 kg ha,1 MB:Pic (98:2) sealed with high-density polyethylene (HDPE) film. However, the primary alternative chemical, 1,3-dichloropropene (1,3-D), tended to provide slightly lower pest control even on sites with relatively low plant parasitic nematode, soil-borne pathogen and weed pest pressure. CONCLUSION: If California regulations change to allow the use of low-permeability films in broadcast fumigant applications, the results of this research suggest that reduced rates of MB in perennial crop nurseries could serve as a bridge strategy until more technically, economically and environmentally acceptable alternatives are developed. Published 2010 by John Wiley & Sons, Ltd. [source] Thermal and morphological characterization of composites prepared by solution crystallization method of high-density polyethylene on carbon nanotubesPOLYMER COMPOSITES, Issue 5 2010Linghao He The morphology, nucleation, and crystallization of polyethylene/carbon nanotubes composites prepared by solution crystallization method of high density polyethylene on Multiwall Carbon Nanotubes (MWNTs) are studied. Transmission electron microscopy (TEM) results show that the center stems of MWNTs are decorated with lamellar crystals. The nonisothermal crystallization kinetics of pure PE and PE/MWNTs composites are investigated by differential scanning calorimetry at various cooling rates. It is found that the Avrami analysis modified by Jeziorny and Mo can describe the nonisothermal crystallization process of pure PE and PE/MWNTs very well. The difference in the value of exponent between PE and PE/MWNTs suggests that addition of the MWNTs influences the mechanism of nucleation and the growth of PE crystallites. On one hand, the increasing of temperature corresponding to the maximum rate of crystallization and the onset crystallization temperature and the study of the nucleation activity reveal that the inorganic component (MWNTs) can act as the nucleating agent to facilitate the crystallization of PE in the hybrids. On the other hand, the decreasing degree of crystallinity and the increasing of half-crystallization time imply that the MWNTs networks confine the crystallization of PE. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers [source] Investigation of oxygen barrier properties of organoclay/HDPE/EVA nanocomposite films prepared using a two-step solution methodPOLYMER COMPOSITES, Issue 6 2009S.M. Reza Dadfar In this article, oxygen barrier properties of nanocomposite films composed of organoclay (OC), high-density polyethylene (HDPE), and ethylene vinyl acetate (EVA) copolymer have been investigated. The nanocomposite films whose EVA forms a dominant fraction were prepared using the solution method. The dispersion of the OC in the HDPE/EVA blend was improved through taking two-step procedure in the preparation of nanocomposite. First, the OC and EVA were dissolved in chloroform. Then, the resulting product, after evaporating most of the solvent, along with HDPE was dissolved in xylene. The obtained nanocomposite films underwent a number of tests in order to examine their barrier properties including X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results showed that OC/HDPE/EVA nanocomposites are intercalated and partially exfoliated. Furthermore, from the TEM micrographs, the organoclay experimental aspect ratio was found. Also, the O2 permeability through the films was evaluated, which showed that adding both OC and HDPE to EVA leads to a remarkable increase in the barrier properties of EVA films. Finally, by using the gas permeation results and existing permeation theories, the organoclay theoretical aspect ratio was predicted. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source] Effect of high-energy vibro-milling of filler on the mechanical properties of filled high-density polyethylenePOLYMER COMPOSITES, Issue 3 2003Shaoyun Guo The effect of high-energy mechanical milling of CaCO3 (calcium carbonate) and STC (a mixture of sericite, tridymite and cristobalite) on mechanical properties, rheological and dynamical mechanical behavior of high-density polyethylene (HDPE)/CaCO3 and HDPE/STC was studied through SEM (scanning electron microscope), DMTA (dynastic mechanical test analysis), mechanical and melt rheological properties tests. The experimental results show that addition of fillers treated by coupling agent and vibromilling to HDPE makes the impact strength of HDPE greatly increased. The impact strength of HDPE/treated CaCO3 (60/40) and HDPE/treated STC (60/40) is ca. 4 and 3 times respectively as high as that of HDPE. The SEM micrographs of impact fractured surfaces of treated fillers filled HDPE show extensive plastic deformation of HDPE matrix, indicating that the plastic deformation of matrix induced by the treated fillers is the main contribution for absorbing a great amount of impact energy. This is the reason why the impact strength of HDPE greatly increases with addition of coupling agent and vibromilling treated fillers. The intensity of , relaxation peak of HDPE in HDPE/treated CaCO3 on tan, vs. temperature curve increases and the peak shifts to higher temperature due to its stronger interface interaction as compared with that of HDPE/untreated CaCO3. [source] Mechanical behavior of cold plasma,treated sisal and high-density polyethylene compositesPOLYMER COMPOSITES, Issue 3 2003Adriana R. Martin Sisal fibers and finely powdered high-density polyethylene were surface functionalized with dichlorosilane on a RF(radio frequency)-plasma reactor. Composites made from sisal and high-density polyethylene were compounded using a thermokinetic mixer. The discharged mass was cooled, granulated, and injected molded into composite specimens for testing. The mechanical behaviors (tensile, impact and thermal dynamical mechanical properties) of composites made from cold plasma-treated and untreated components are compared and discussed. The best mechanical performance was generally obtained for composites where only the inert thermoplastic matrix was plasma-functionalized. Plasma treatment of lignocellulosic fibers seems to induce decomposition processes of the surface layers structures exposed to the plasma that generally does not contribute to significant improvement on the mechanical behavior of the composite. [source] Adhesion improvement in glass fiber reinforced polyethylene composite via admicellar polymerizationPOLYMER COMPOSITES, Issue 1 2003Usa Somnuk Admicellar polymerization (polymerization of monomer solubilized in adsorbed surfactant bilayers) has been used to form a thin film of polyethylene onto the surface of milled glass fibers using sodium dodecyl sulfate as the surfactant. The decrease in ethylene pressure was used to follow the solubilization and adsolubilization processes as well as the reaction processes. An increase in initiator (Na2S2O8) to surfactant ratio gave thicker and more uniform coatings of polymer onto the glass fiber surface according to SEM micrographs. Although a substantial amount of ethylene polymerized in solution according to the pressure drop, the decrease in pressure attributed to admicelle polymerization corresponded to the amount of polymer formed on the glass fiber, indicating little, if any, solution polymer deposited on the fibers. The admicellar-treated glass fiber was used to make composites with high-density polyethylene. The composites showed an increase in tensile and flexural strength over composites made from as-received glass fiber, indicating an improvement in the fiber-matrix adhesion of the admicellar-treated glass fiber. [source] | ||||||||||||||||