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MPa Pressure (mpa + pressure)
Selected AbstractsCrystallization effects on autoclave foaming of polycarbonate using supercritical carbon dioxideADVANCES IN POLYMER TECHNOLOGY, Issue 4 2006L. Mascia Abstract In this study, the conditions leading to the formation of cells and to the onset of crystallization of polycarbonate were examined with the use of supercritical carbon dioxide for the production of foams from preforms. Small plaques cut from extruded sheets were treated with supercritical carbon dioxide in an autoclave at temperatures varying from 60 to 200°C and from 4.5 to 30 MPa pressure. Visual observations and stereoscan electron microscopy examination revealed that penetration of supercritical carbon dioxide takes place via the advancing layer mechanism and that, for the particular grade of polycarbonate used in this study, the nucleation of the cells can take place at temperatures as low as 60°C. It requires, however, long treatment times and high pressures, and the growth of foam cells is severely restricted. Nucleation and growth of cells occurred much more readily at somewhat higher temperatures. With treatments at around 80°C, the onset of crystallization started to impose considerable hindrance to the formation of uniform and evenly distributed cells. This becomes increasingly evident at higher temperatures, between 100 and 180°C, owing to the formation of large spherulitic crystalline domains. A very effective nucleation and growth mechanism for the formation of cells was obtained, on the other hand, with treatments at 200°C due to the absence of crystallization phenomena. The degree of crystallinity increased with increasing treatment temperature, and the resulting morphology gave rise to two broad melting peaks. These are displaced to higher temperatures and become closer, merging into one peak with a low-temperature shoulder. These events were monitored by thermal analysis and wide-angle X-ray diffraction examinations. © 2007 Wiley Periodicals, Inc. Adv Polym Techn 25:225,235, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20075 [source] Accelerated ageing of polypropylene stabilized by phenolic antioxidants under high oxygen pressureJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Emmanuel Richaud Abstract Polypropylene (PP) samples stabilized by a hindered phenol (Irganox 1010) were submitted to thermal ageing at 80°C in air at atmospheric pressure or in pure oxygen at 5.0 MPa pressure. Both the polymer oxidation and the stabilizer consumption were monitored by Infrared spectrometry and thermal analysis. The stabilizer efficiency, as assessed by the ratio induction time/stabilizer concentration is almost constant at atmospheric pressure even when the stabilizer concentration is higher than its solubility limit in PP (0.4% or 24 × 10,3 mol L,1). In contrast, at high pressure, the efficiency decreases almost hyperbolically with the stabilizer concentration when this latter is higher than 6.0 × 10,3 mol L,1. The results indicate the existence of a direct phenol-oxygen reaction negligible at low oxygen pressure but significant at 5.0 MPa pressure. The reality of this reaction has been proved on the basis of a study of the thermal oxidation of a phenol solution in a nonoxidizable solvent. A kinetic model of PP oxidation in which stabilization involves three reactions has been proposed. It simulates correctly the effect of oxygen pressure and stabilizer concentration on carbonyl build-up and stabilizer consumption. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Application of poly(acrylic acid) superporous hydrogel microparticles as a super-disintegrant in fast-disintegrating tabletsJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 4 2004Shicheng Yang ABSTRACT Poly(acrylic acid) superporous hydrogel (SPH) microparticles possessing a unique porous structure were used as a wicking agent to decrease disintegration time of fast-disintegrating tablets (FDTs). The compression behaviour of poly(acrylic acid) SPH microparticles was evaluated using the Kawakita equation. Effects of various SPH microparticle sizes and a 19-run fractional factorial design were evaluated. The factorial design was based on four factors consisting of ketoprofen, SPH microparticle, filler, and tableting pressure, and each factor contained three levels on the disintegration time and tensile strength of the prepared FDTs. The poly(acrylic acid) SPH microparticles existed in an amorphous state and swelled approximately 80-times in distilled water and 50-times in pH 6.8 0.2 m phosphate buffer. The compressibility of SPH microparticles increased significantly as the microparticle size increased. The FDTs made of SPH microparticles in the range of 75,106 ,m showed the fastest disintegration time and higher tensile strength. SPH microparticle, tableting pressure and ketoprofen had significant effects on disintegration time and tensile strength of ketoprofen FDTs. The FDTs that were prepared with 2.5% w/w SPH microparticles of 75,106 ,m at 63 MPa pressure possessed a tensile strength of 84.4+4.1 N cm,2 and disintegrated in 15.0+2.0 s. It was concluded that the poly(acrylic acid) SPH microparticles could serve as a good super-disintegrant decreasing the disintegration time of FDTs. [source] Hydrothermal Synthesis of Alpha Alumina (,-Al2O3) Powders: Study of the Processing Variables and Growth MechanismsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2010Wojciech L. Suchanek Alpha alumina (,-Al2O3) powders and ,-Al2O3/boehmite (,-AlOOH) mixtures with controlled ,-AlOOH contents were synthesized hydrothermally under alkaline or acidic conditions at 380°,435°C for 1,10 days, under 6.9,14.5 MPa pressure, from concentrated precursors without stirring. The precursors were formed by mixing different types of aluminum hydroxides with water, and optionally with ,-Al2O3 seeds, hydrogen peroxide, sulfuric acid, dopants (i.e., KMnO4), and/or other additives. The experiments were performed on industrial scale in large production autoclaves. The synthesized ,-Al2O3 powders exhibited up to 100% phase purity, 99.98% chemical purity, equiaxed morphology, low aggregation levels, narrow crystallite size distributions with primary particle sizes ranging between 100 nm and 40 ,m, and high reproducibility. Precursor types, seeds, chemical additives, and temperature/time of the hydrothermal synthesis were found to govern properties of the powders. Different growth mechanisms for nanosized and rough powders are discussed. Results of this study enable the use of hydrothermal ,-Al2O3 powders in a multitude of applications, and make their hydrothermal production a commercial reality. [source] Distribution of Cerium Ions in Cerium-Doped ,,-SiAlON and Its Effect on Grain MorphologyJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2002Fang-Fang Xu Cerium-doped ,,-SiAlON material was prepared by spark plasma sintering at 1750°C under 30 MPa pressure for 10 min. Yttrium ,,-SiAlON seeds (1 wt%) were added to the starting powder mixture. Recent work showed that up to 45 wt% of ,,-SiAlON phases are formed in the present sintered ceramics. The material presented a microstructure, containing rodlike cerium-doped ,,-SiAlON crystals. In this paper, transmission electron microscopy and energy dispersive spectroscopy examinations of the ,,-SiAlON grains are reported. The structural analyses revealed a high density of domain boundaries, within which larger amounts of cerium ions were segregated than in the matrix. The density of the domain boundaries was proportional to the amount of incorporated cerium ions. These structural defects eventually dominated the growth habits of the ,,-SiAlON crystals, by modifying the structure of the interstices at the boundary sites. The role of yttrium ,,-SiAlON seeds also is discussed in this paper. [source] Morphology and Crystalline Structure of Poly(, -Caprolactone) Nanofiber via Porous Aluminium Oxide TemplateMACROMOLECULAR MATERIALS & ENGINEERING, Issue 9 2006Yang Chen Abstract Summary: Poly(, -caprolactone) (PCL) nanofibers with a dimension of about 150 nm were successfully fabricated by using a process of extruding PCL solution via a porous aluminium oxide template and then solidifying in methanol. The morphology, melting behavior and crystalline structure of the nanofibers were investigated by using scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and X-ray diffraction (XRD). The results revealed that the weight-average molecular weight () of PCL hardly influenced the morphology of the nanofibers. However, the melting temperature (Tm) of the PCL crystalline increased slightly from 55.4 to 57.5,°C with an increase in . The accessional pressure and the presence of the porous template played an important role in the improvement of the orientation and crystallization structures of the polymer chains when they were passing through the nano-scale porous channel, leading to the conglomeration of the fiber and the much larger diameter than those from the pressure-induced extrusion process. Furthermore, comparing the processes with and without accessional pressure, the crystallinity of the nanofibers obtained under 0.2 MPa pressure increased, and the diffraction for the (001) lattice plane occurred. SEM image of PCL nanofibers extruded via a porous aluminium oxide template with the aid of pressure. [source] Microbial Inactivation Kinetics during High-Pressure Carbon Dioxide Treatment: Nonlinear Model for the Combined Effect of Temperature and Pressure in Apple JuiceJOURNAL OF FOOD SCIENCE, Issue 8 2008G. Ferrentino ABSTRACT:, Isobaric and isothermal semi-logarithmic survival curves of natural microflora in apple juice treated with high-pressure carbon dioxide at 7, 13, and 16 MPa pressures and 35, 50, and 60 °C temperatures were fitted with a nonlinear equation to find the values of the coefficient b(P ), b(T ), n(P ), and n(T ). Profiles of the model parameters were obtained as a function of pressure and temperature. The model fitted with good agreement (R2 > 0.945), the survival curves. An empirical equation was proposed to describe the combined effects of pressure and temperature. The equation, derived from a power law model, was written in the form: . The proposed model fitted the experimental data well. At 7 MPa and 50 and 60 °C, 13 MPa and 35 and 60 °C, 16 MPa and 35 °C, the model provided log10 reduction residual values (observed value , fitted value) lower than 0.284 showing a good agreement between the experimental and the predicted survival levels. [source] | |||||||||||||