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Solubility Limit (solubility + limit)
Selected AbstractsInfluence of sediment ingestion and exposure concentration on the bioavailable fraction of sediment-associated tetrachlorobiphenyl in oligochaetes,ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 4 2008Arto J. Sormunen Abstract The desorption and bioavailability of 3,3,,4,4,-tetrachlorobiphenyl (PCB 77) were studied in spiked natural sediments at six concentrations. The desorption kinetics were measured in a sediment,water suspension using Tenax® resin extraction, and the bioavailability was measured by exposing Lumbriculus variegatus (Oligochaeta) to PCB 77,spiked sediment in a 14-d kinetic study. In addition, freely dissolved pore-water concentrations were measured using the polyoxymethylene solid-phase extraction method. The present study examined whether bioavailability can be defined more accurately by measuring the size of desorbing fractions and the pore-water concentrations than by using the standard equilibrium partitioning approach. The importance of ingested sediment in bioaccumulation also was investigated. Our data showed a clear, decreasing trend in the rapid-desorbing fractions and in the standard biota,sediment accumulation factors (BSAF) with increasing concentration in sediment. Desorbing fractions,refined BSAFs were more uniform across the concentration treatments, and the pore-water PCB 77 concentration predicted tissue concentrations close to observed values. In the risk assessment process, pore-water concentration or desorbing fractions would lead to more precise bioavailability estimates compared with those from the traditional equilibrium partitioning approach. The result also showed, however, that sediment-ingesting worms had access to an additional bioavailable chemical fraction that was especially evident when PCB 77 pore-water concentrations most likely approached the solubility limit. Thus, feeding may modify the bioavailable fraction that cannot be explained by simple equilibrium partitioning models. [source] Global Techniques for Characterizing Phase Transformations , A Tutorial ReviewADVANCED ENGINEERING MATERIALS, Issue 6 2010Michel Perez To characterize phase transformations, it is necessary to get both local and global information. No experimental technique alone is capable of providing these two types of information. Local techniques are very useful to get information on morphology and chemistry but fail to deal with global information like phase fraction and size distribution since the analyzed volume is very limited. This is why, it is important to use, in parallel, global experimental techniques, that investigate the response of the whole sample to a stimulus (electrical, thermal, mechanical,). The aim of this paper is not to give an exhaustive list of all global experimental techniques, but to focus on a few examples of recent studies dealing with the characterization of phase transformations, namely (i) the measurement of the solubility limit of copper in iron, (ii) the tempering of martensite, (iii) the control of the crystallinity degree of a ultra high molecular weight polyethylene and (iii) a precipitation sequence in aluminum alloys. Along these examples, it will be emphasized that any global technique requires a calibration stage and some modeling to connect the measured signal with the investigated information. [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] Terephthalic acid synthesis at higher concentrations in high-temperature liquid water.AICHE JOURNAL, Issue 6 2009Abstract We synthesized terephthalic acid (TPA) from p -xylene at an initial concentration above its solubility limit in high-temperature liquid water (HTW). The nominal p -xylene loading at the reaction conditions was 0.4 mol L,1, which is the highest reported to date for generation of high TPA yields (>70 mol %) in HTW. The presence of two liquid phases during the reaction did not appear to accelerate the rate, unlike behavior reported for some other organic reactions done "on water" at lower temperatures. Adding oxygen gas in a large increment during synthesis produced a black liquid and a black solid byproduct, which is a previously undocumented problem. Adding oxygen in smaller increments prevented formation of the liquid and solid byproducts and also provided high selectivities (90 mol %) and yields (>70 mol %) of TPA. These results demonstrate the feasibility of HTW as a medium for TPA synthesis at p -xylene concentrations even higher than its solubility limit. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Hot Isostatic Pressing of Transparent Nd:YAG CeramicsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2009Sang-Ho Lee This paper demonstrates that fine-grained (2,3 ,m), transparent Nd:YAG can be achieved at SiO2 doping levels as low as 0.02 wt% by the sinter plus hot isostatic pressing (HIP) approach. Fine grain size is assured by sintering to 98% density, in order to limit grain growth, followed by HIP. Unlike dry-pressed samples, tape-cast samples were free of large, agglomerate-related pores after sintering, and thus high transparency (i.e., >80% transmission at 1064 nm) could be achieved by HIP at <1750°C along with lower silica levels, thereby avoiding conditions shown to cause exaggerated grain growth. Grain growth was substantially limited at lower SiO2 levels because silica is soluble in the YAG lattice up to ,0.02,0.1 wt% at 1750°C, thus allowing sintering and grain growth to occur by solid-state diffusional processes. In contrast, liquid phase enhanced densification and grain growth occur at ,0.08,0.14 wt% SiO2, especially at higher temperatures, because the SiO2 solubility limit is exceeded. [source] Phase Relations and Thermal Expansion Studies in the Ceria,Yttria SystemJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2004Sandeep V. Chavan The synthesis, characterization, and bulk and lattice thermal expansions of a series of compounds with general composition Ce1,xYxO2,x/2 (0.0 ,x, 1.0) are reported. The XRD pattern of each product was refined to learn the solid solubility limit and the homogeneity range. The solid solubility limit of YO1.5 in CeO2 lattice, under the conditions of slow cooling from 1400°C, is represented as Ce0.55Y0.45O1.775 (i.e., 45 mol% of YO1.5). The subsequent compositions were biphase. There was no solubility of CeO2 into the lattice of YO1.5. The bulk thermal expansion measurements from ambient to 1123 K, as investigated using a dilatometer, revealed that the ,l (293,1123 K) values, within the homogeneity range, decreased on increased Y3+ content. A similar trend was observed for average lattice thermal expansion coefficient, ,a (293,1473 K), as investigated using high-temperature XRD. No ordered phases were obtained in this system under the used conditions. These studies on Ce1,xYxO2,x/2 (0.0 ,x, 1.0) system can be used to simulate the phase relation and thermal expansion behavior of Pu1,xYxO2,x/2 (0.0 ,x, 1.0), because CeO2 is widely used as a surrogate material for PuO2. [source] ZnCdO/ZnO , a new heterosystem for green-wavelength semiconductor lasingLASER & PHOTONICS REVIEWS, Issue 3 2009S. Kalusniak Abstract We report on our efforts to cultivate the ternary compound ZnCdO as a semiconductor laser material. Molecular beam epitaxy far from thermal equilibrium allows us to overcome the standard solubility limit and to fabricate alloys with band gaps ranging from 3.4 down to 2.1 eV. Optimized structures containing well-defined quantum wells as active zones are capable of low-threshold lasing under optical pumping up to room temperature. The longest lasing wavelength achieved so far is 510 nm. [source] In-situ doping and implantation of GaN layers with MnPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue S2 2009k Sofer Abstract In this paper we present a growth of Ga1,xMnxN layers by MOVPE and ion implantation of GaN layers with Mn. The Mn concentration detected by electron microprobe and PIXE was well below the solubility limit, ranging from 0.2 to 1.1 at.%. Implanted doses of Mn ions were in the range 1x1016 -5x1016 Mn atoms.cm,2 with energy of 330 keV. The analysis of the MOVPE deposition process of Ga1,xMnxN thin films revealed an unfavorable ratio between the apparent Mn concentration in the gas phase and its doping level in the deposited layer. On the other hand, the incorporation of Mn has a positive effect on the resulting surface morphology. The optimal deposition temperature of 1000 °C was found out as a compromise between the layer quality and Mn concentration. In both in-situ grown and implanted samples, a ferromagnetic component persisting up to room temperature and a prevailing paramagnetic phase were observed. The ferromagnetic moment observed in implanted samples was influenced by free carrier concentration in GaN layers which were used for implantation. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Study of the magnetic disaccommodation in La doped YIGPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 10 2005C. Torres Abstract The relaxation of the initial magnetic permeability of La doped yttrium iron garnet (YIG) samples with nominal composition Y3,xLaxFe5O12 (0< x <0.6) is analysed in this work. The results show a very different behaviour depending on the sintering atmosphere used for the fabrication of the samples. Concretely, for the samples sintered in air, it just have been detected the usual relaxation peak found in YIG at 130 K. However, a new relaxation peak appears around room temperature for the samples sintered in CO2 atmosphere when the La content is at least of 0.3. These results have been interpreted in terms of the formation of a secondary perovskite phase when the La solubility limit is reached. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Thermal and morphological properties of high-density polyethylene/ethylene,vinyl acetate copolymer composites with polyhedral oligomeric silsesquioxane nanostructurePOLYMER INTERNATIONAL, Issue 2 2010Patrícia Scapini Abstract The demand for improved properties of common polymers keeps increasing, and several new approaches have been investigated. In the study reported here, composites with a polymer matrix comprising a blend of high-density polyethylene with ethylene,vinyl acetate copolymer (EVA), and with polyhedral oligomeric silsesquioxane (POSS) as a nanostructure, were processed and characterized in terms of their thermal and morphological properties. For the preparation of the composites, the concentrations of the blend components (0, 50 and 100 wt%) and of the POSS (0, 1 and 5 wt%) were varied. X-ray diffraction results indicated that the presence of EVA in the composites led to the appearance of crystalline domains at lower POSS concentrations. Transmission and scanning electron microscopy showed that samples with 1 wt% of POSS had a homogeneous distribution in the polymer matrix with average dimensions of ca 150 nm. However, the formation of aggregates occurred in samples with 5 wt% of POSS. Differential scanning calorimetry and thermogravimetic analyses indicated that the POSS did not affect the melt and degradation temperatures of the polymer matrix. POSS underwent aggregation at higher concentrations during the composite processing, indicating a solubility limit of around 1 wt%. The presence of EVA in the composite favors POSS aggregation due to an increase in the polarity of the polymer matrix. Copyright © 2009 Society of Chemical Industry [source] Sorption of male hormones by soils and sedimentsENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 2 2007Il Kim Abstract ,This paper reports the sorption of two male hormones, testosterone and androstenedione, by four soil and sediment samples at both equilibrium and rate-limiting conditions. Unlike prior studies, androstenedione was studied independently of testosterone. Apparent sorption equilibrium is achieved in one to two weeks when the initial aqueous hormone concentrations (C0) at 10,000 ,g/L (,30% of their solubility limits [Sw]) and two to three weeks when the C0 is 300 ,g/L (less than 1% of Sw). The Freundlich model parameter n ranged from 0.698 to 0.899 for all soil,solute systems indicating nonlinear sorption isotherms. Isotherm nonlinearity leads to an inverse correlation between single-point organic carbon,normalized sorption distribution coefficients (KOC) and equilibrium androgen concentration (Ce). When Ce/Sw = 0.012, the log KOC values for testosterone and androstenedione on the various sorbents ranged from 6.18 to 6.75 and 6.83 to 6.04, respectively, compared to 6.30 to 6.80 and 6.16 to 6.92 when Ce/Sw = 0.004. This study suggests that male hormones may exhibit slow rates of sorption over 14 d or longer and that soils and sediments may have greater sorption distribution coefficients when concentrations fall into the ng/L range. [source] The Role of Surface and Interface Energy on Phase Stability of Nanosized Insertion CompoundsADVANCED MATERIALS, Issue 25-26 2009Marnix Wagemaker Thermodynamic theory reveals the impact of surface and interface energies on the equilibrium properties and solubility limits of interstitial ions in nanosized crystallites. Applied to LixFePO4 especially interface energy contributions play important roles, and their effect explains observations of the narrowing of electrochemically measured miscibility gaps in nanostructured electrodes. [source] Phase Relations in the Pyrochlore-Rich Part of the Bi2O3,TiO2,Nd2O3 SystemJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2009pela Kunej In this study we used solid-state synthesis to determine the phase relations in the pyrochlore-rich part of the Bi2O3,TiO2,Nd2O3 system at 1100°C. The samples were analyzed using X-ray powder diffraction and scanning electron microscopy with energy- and wavelength-dispersive spectroscopy. A single-phase pyrochlore ceramic was obtained with the addition of 4.5 mol% of Nd2O3. We determined the solubility limits for the three solid solutions: (i) the pyrochlore solid solution Bi(1.6,1.08x)NdxTi2O(6.4+0.3x), where 0.25 Comprehensive Linkage of Defect and Phase Equilibria through Ferroelectric Transition Behavior in BaTiO3 -Based Dielectrics: Part 1.JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2008Defect Energies Under Ambient Air Conditions Defect and phase equilibria have been investigated via the ferroelectric phase transition behavior of pure and equilibrated nonstoichiometric BaTiO3 powder samples. Through fabricating the BaTiO3 materials under highly controlled conditions to preserve the equilibrium conditions with respect to Ba/Ti ratio, annealing temperature (T), and oxygen partial pressure (PO2), systematic variations in the phase transition temperature can be noted with respect to Ba/Ti ratio and T. From the data extracted, we can then determine solubility limits. Equilibrating the defect reactions at the solubility limits provides a direct approach to identify and calculate the defect energetics. The phase transition temperature decreased with increasing concentration of the TiO2 partial-Schottky defects (BaTi1,,O3,2,) and the BaO partial-Schottky defects (Ba1,,TiO3,,), and showed discontinuous changes in the two-phase region. The formation enthalpy and entropy for the partial-Schottky defect reactions was evaluated to be 2.32±0.1 eV and 10.15±0.7 kB for the BaO partial-Schottky defect, and 2.89±0.1 eV and 8.0±1.5 kB for the TiO2 partial-Schottky defects equilibrated under air annealing conditions. [source]
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