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Nucleation Density (nucleation + density)
Selected AbstractsCrystalline morphology and dynamical crystallization of antibacterial ,-polypropylene compositeJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Xin Chen Abstract The crystalline morphology and dynamical crystallization of antibacterial polypropylene composite and pure polypropylene were investigated via differential scanning calorimeter (DSC), wide angle X-ray diffraction (WAXD), and real-time hot-stage optical microscopy (OM). The results reveal that the crystalline morphology of antibacterial PP composites changes with variations of the crystallization conditions and compositions. The crystalline phase consists of both ,-PP and ,-PP crystals. The content of ,-PP decreases with the increase in antibacterial agent content and cooling rate. With the addition of ,-nucleating agent, the morphologies of all dynamically crystallized antibacterial PP composites show no obvious spherulitic morphology, and the decrease of crystal perfection and the increase of nucleation density of antibacterial PP composite system could be observed. With the increase of antibacterial agent content, the overall crystallization rates of the antibacterial PP composite increase dramatically, while the content of ,-PP in all antibacterial PP composite decrease distinctly under given cooling conditions. These results can be explained by the interruptive effect of antibacterial agent on interactions of ,-nucleating agent components and the obstructing effect of antibacterial agent on the mobility of PP chains in melts. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Crystallization of poly(butylene terephthalate)/poly(ethylene octene) blends: Nonisothermal crystallizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008Jiann-Wen Huang Abstract Poly(ethylene octene) (POE), maleic anhydride grafted poly(ethylene octene) (mPOE), and a mixture of POE and mPOE were added to poly(butylene terephthalate) (PBT) to prepare PBT/POE (20 wt % POE), PBT/mPOE (20 wt % mPOE), and PBT/mPOE/POE (10 wt % mPOE and 10 wt % POE) blends with an extruder. The melting behavior of neat PBT and its blends nonisothermally crystallized from the melt was investigated with differential scanning calorimetry (DSC). Subsequent DSC scans exhibited two melting endotherms (TmI and TmII). TmI was attributed to the melting of the crystals grown by normal primary crystallization, and TmII was due to the melting of the more perfect crystals after reorganization during the DSC heating scan. The better dispersed second phases and higher cooling rate made the crystals that grew in normal primary crystallization less perfect and relatively prone to be organized during the DSC scan. The effects of POE and mPOE on the nonisothermal crystallization process were delineated by kinetic models. The dispersed phase hindered the crystallization; however, the well- dispersed phases of an even smaller size enhanced crystallization because of the higher nucleation density. The nucleation parameter, estimated from the modified Lauritzen,Hoffman equation, showed the same results. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Contrasting textural record of two distinct metamorphic events of similar P,T conditions and different durationsJOURNAL OF METAMORPHIC GEOLOGY, Issue 8 2005O. LEXA Abstract A structural, metamorphic and geochronological study of the Staré M,sto belt implies the existence of two distinct metamorphic events of similar peak P,T conditions (700,800 °C, 8,10 kbar) during the Cambro-Ordovician and the Carboniferous tectonometamorphic events. The hypothesis of two distinct periods of metamorphism was suggested on the basis of structural discordance between an undoubtedly Carboniferous granodiorite sill intrusion and earlier Cambro-Ordovician fabrics of a banded amphibolite complex. The analysis of crystal size distribution (CSD) shows high nucleation density (N0) and low average growth rate (Gt) for Carboniferous mylonitic metagabbros and mylonitic granodiorites. The parameter N0 decreases whereas the quantity Gt increases towards higher temperatures progressively approaching the values obtained from the Cambro-Ordovician banded amphibolite complex. The spatial distribution of amphibole and plagioclase shows intense mechanical mixing for lower-temperature mylonitic metagabbros. In high-temperature mylonites a strong aggregate distribution is developed. Cambro-Ordovician amphibolites unaffected by Carboniferous deformation show a regular to anticlustered spatial distribution resulting from heterogeneous nucleation of individual phases. This pattern, together with CSD, was subsequently modified by the grain growth and textural equilibration controlled by diffusive mass transfer during Carboniferous metamorphism. The differences between the observed textures of the amphibolites are interpreted to be a consequence of the different durations of the Carboniferous and Cambro-Ordovician thermal events. [source] Diamond Growth on a Si Substrate With Ceramic InterlayersJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 5 2007Y. S. Li Deposition of diamond films on Si substrates precoated with a series of ceramic intermediate layers was examined. The interlayers containing SiC, SiNx, SiCN, TiSiN, and TiAlSiN were prepared by a liquid injection plasma-enhanced chemical vapor deposition (PECVD) method using alkoxide solution precursors. The subsequent diamond synthesis on these coatings was carried out by microwave plasma-assisted CVD (MPCVD) using a H2,1%CH4 mixture. A higher nucleation density of diamond was obtained on these intermediate layers than on the as-polished Si wafer, along with a nonuniform surface distribution of diamond. Diamond powder scratching pretreatment of these interlayers enhanced the nucleation density and promoted the formation of fully uniform diamond films. Particularly, nanocrystalline diamond films were directly generated on TiSiN and TiAlSiN layers under an identical deposition condition that had favored the formation of microcrystalline diamond films on Si wafers and the Si(C,N) interlayers. The mechanism for this difference is attributed primarily to a higher amount of residual amorphous carbon in TiSiN and TiAlSiN layers than that inside Si(C,N) layers. [source] Using Chitosan as a Nucleation Agent in Thermoplastic Foams for Heavy Metal AdsorptionMACROMOLECULAR SYMPOSIA, Issue 1 2009Milton O. Vázquez Abstract Thermoplastics/chitosan-powder composite foams were prepared by extrusion using azodicarbonamide (ACA) as chemical blowing agent. The effect of chitosan content on morphology (cell size, nucleation density and foam density) of the foams was studied. Chitosan particles are located on the bubbles periphery. Morphological quantification showed that foam cell size decreased and cell population increased with addition of chitosan into polymeric matrix from 1 to 10%. Further, optimum chitosan content was obtained for each polymer. Polymers foamed with chitosan were tested as a chelating resin to adsorb chromium (Cr VI) from different concentration solutions. [source] Designing the Si(100) conversion into SiC(100) by GePHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 2 2010Richard Nader Abstract The deposition of Germanium (Ge) prior to the conversion of Si(100) into 3C-SiC(100) results in changes of the structure and surface morphology of the formed silicon carbide layer. First of all it reduces the thickness of the 3C-SiC layer grown during the conversion process and therefore the probability of voids formation. Secondly, it increases the nucleation density of the formed 3C-SiC nuclei and therefore, decreases the grain size at Ge coverages below two monolayers. These affect the roughness of the SiC surface positively by modifying the width of the SiC-Si interface. If the Ge coverages exceed two monolayers the structural and morphological properties begin to degrade. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Numerical modeling of nonisothermal polymer crystallization kinetics: Flow and thermal effectsPOLYMER ENGINEERING & SCIENCE, Issue 10 2010Matthieu Zinet A numerical model able to simulate polymer crystallization under nonisothermal flows is developed. It is based on the assumption that the trace of the extra-stress tensor, calculated according to a viscoelastic multimode Upper Convected Maxwell (UCM) model, is the driving force of the flow-induced extra nucleation. Two distinct sets of Schneider equations are used to describe the growth of thermally and flow induced nuclei. The model is then coupled with the momentum equations and the energy equation. As an application, a shear flow configuration between two plates (Couette flow) is simulated. The relative influence of the mechanical and thermal phenomena on the crystallization development as well as the final morphology distribution is then analyzed as a function of the shearing intensity and the cooling kinetics, in terms of nucleation density and crystallite mean sizes. POLYM. ENG. SCI., 50:2044,2059, 2010. © 2010 Society of Plastics Engineers [source] Effect of thermomechanical history on the crystallization of poly(ether- block -amide)POLYMER ENGINEERING & SCIENCE, Issue 12 2008Bruno Tavernier The quiescent and flow-induced crystallization of a poly(ether- block -amide) is studied by means of rheo-optical methods. Both optical microscopy and small angle light scattering have been used. The multiblock copolymer has a microphase-separated structure with an order,disorder transition at 180,185°C, as measured with rheometry and SAXS. The number of nuclei, spherulitic growth rates, and the characteristic time scale for crystallization are compared with that of a polyamide of similar molar mass. For the poly(ether- block -amide),containing a majority of amide segments,the growth rates of the spherulites during quiescent crystallization are similar for the block copolymer and the homopolymer, even if the spherulitic structures are not the same. When flow is applied, the two materials behave differently. The flow increased the nucleation density in the homopolymer but not in the block copolymer. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Polyolefin nanocomposites: Essential work of fracture analysisPOLYMER ENGINEERING & SCIENCE, Issue 6 2004M. N. Bureau The tensile properties and the fracture toughness, based on the essential work of fracture (EWF) method, of melt-compounded polymer nanocomposites based on polypropylene (PP) with organo-modified clays (montmorillonite) and maleic anhydride (MA),grafted PP coupling agents were studied. Depending on the compounding sequence and on whether a coupling agent was used, some improvements in tensile properties were observed. These improvements were related to the level of dispersion of clay particles. The highest tensile properties were obtained for the PP/clay compound showing the highest surface density of uniform sub-micron particles. The mechanical improvements of the PP/clay compounds were those of a microcomposite in which the fiber reinforcement has an average aspect ratio of 17,35. The PP/clay compounds with coupling agents and with highest surface density of uniform sub-micron particles showed very good fracture toughness, with EWF values slightly higher than those of unfilled PP. Fractographic observations showed that clay particles acted as void nucleation sites, which then grew and coalesced, promoting fibrillation of the remaining material between the voids. The EWF results indicated that the void nucleation density determined the fracture toughness. The EWF results also indicated that the plastic work dissipation related to the stability of the fibrillation, which was promoted by the use of a coupling agent. Polym. Eng. Sci. 44:1142,1151, 2004. © 2004 Society of Plastics Engineers. [source] | ||||||||||