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Temperature.
Kinds of Temperature. Selected AbstractsCombined effects of crucible geometry and Marangoni convection on silicon Czochralski crystal growthCRYSTAL RESEARCH AND TECHNOLOGY, Issue 8 2009F. Mokhtari Abstract In order to understand the influence of crucible geometry combined with natural convection and Marangoni convection on melt flow pattern, temperature and pressure fields in silicon Czochralski crystal growth process, a set of numerical simulations was conducted. We carry out calculation enable us to determine temperature, pressure and velocity fields in function of Grashof and Marangoni numbers. The essential results show that the hemispherical geometry of crucible seems to be adapted for the growth of a good quality crystal and the pressure field is strongly affected by natural and Marangoni convection and it is more sensitive than temperature. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Micronization of the officinal component baicalin by SEDS-PA processCRYSTAL RESEARCH AND TECHNOLOGY, Issue 6 2007Wen Zhi He Abstract Application of micronizing technologies in processing Chinese herbal medicines is very important to improve the forms of prepared Chinese herbal medicines and promote their therapeutic efficacy. Baicalin, a major active component of the typical Chinese herb medicine Scullateria baicallensis Georgi, was micronized using the Solution Enhanced Dispersion by Supercritical fluids though Prefilming Atomization (SEDS-PA) process with the aim of evaluating the efficiency of applying supercritical fluid precipitation technologies in Chinese herb medicine. This study has shown that acicula or rod-like baicalin crystals with Particle Size (PS) of about 20×100 ,m were successfully micronized by the SEDS-PA process to long rod-like, twisted fiber-like or fibrous net-like microparticles with PS of 0.1-2.2 ,m in width within the range of experiments performed. It was found that a substantial reduction of baicalin microparticles' sizes could lead to a marked increase of adhesions among them and subsequent microparticles agglomeration. With the increase of supercritical CO2 flow rate and the decrease of solution concentration and solution flow rate, smaller and much more agglomerated microparticles were obtained. Increasing pressure led to formation of smaller microparticles. A larger tendency of particles agglomeration was produced at a higher temperature. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Photoelectrical properties of crystalline titanium dioxide thin films after thermo-annealingCRYSTAL RESEARCH AND TECHNOLOGY, Issue 5 2007R. Sathyamoorthy Abstract This paper reports the photoelectrical properties of sol gel derived titanium dioxide (TiO2) thin films annealed at different temperatures (425-900°C). The structure of the as-grown film was found to be amorphous and it transforms to crystalline upon annealing. The trap levels are studied by thermally stimulated current (TSC) measurements. A single trap level with activation energy of 1.5 eV was identified. The steady state and transient photocurrent was measured and the results are discussed on the basis of structural transformation. The photocurrent was found to be maximum for the films annealed at 425°C and further it decreases with annealing at higher temperatures. The photoconduction parameters such as carrier lifetime, lifetime decay constant and photosensitivity were calculated and the results are discussed as a function of annealing temperature. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Determination of lattice parameters and thermal expansion of CuGe2P3 + 0.2 Ge3P4 at elevated temperaturesCRYSTAL RESEARCH AND TECHNOLOGY, Issue 9 2006G. Bhikshamaiah Abstract CuGe2P3 is a p-type semiconductor with zincblende structure. Ge3P4 is soluble up to 35 mole% in CuGe2P3. Lattice parameters of CuGe2P3 + 0.2 Ge3P4 have been determined at elevated temperatures from room temperature to 873 K using the x-ray diffraction profiles (111), (200), (220), (311), (222), (400), (331), (420), (422) and (511) obtained from high temperature diffractometer. It is found that the lattice parameter increases linearly from 0.53856 nm at RT to 0.54025 nm at 873 K. The data on lattice parameter is used and coefficient of lattice thermal expansion of CuGe2P3 +0.2 Ge3P4 was determined at different temperatures. It is found that the coefficient of thermal expansion of CuGe2P3 +0.2 Ge3P4 is 5.48 x 10 -6 K -1 and is independent of temperature. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Thermal properties of conduction current and carrier behavior in an organic electroluminescent deviceELECTRONICS & COMMUNICATIONS IN JAPAN, Issue 3 2009Masahiro Minagawa Abstract Organic electroluminescent device (OLED) was fabricated using a vacuum evaporation method and thermal properties were investigated. The OLED has an indium tin oxide (ITO)/N,N,-diphenyl- N,N,-bis(3-methylphenyl)-1,1,-biphenyl-4,4,-diamine (TPD)/tris(8-hydroxyquinoline) aluminum (Alq)/lithium fluoride (LiF)/aluminum (Al) structure. An electron-dominant device of Al/Alq/LiF/Al structure, or a hole-dominant device of ITO/TPD/Al structure was also fabricated in order to study the carrier behavior in the OLEDs. The current density versus voltage (J,V) properties with various thickness of organic layers were investigated in both electron- and hole-dominant devices, and the thermal dependence of J,V properties was observed in the devices. At room temperature, conductions in a wide current region were considered to be due to space-charge-limited current for all of the devices. Especially for the Al/Alq/LiF/Al device and the OLED, relationships were observed across a wide current region. At low temperature, tunnel currents were estimated for the ITO/TPD/Al device. For the Al/Alq/LiF/Al device and the OLED, relationships were observed across a wide current region at low temperature. © 2009 Wiley Periodicals, Inc. Electron Comm Jpn, 92(3): 24,31, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/ecj.10048 [source] Thermoelectric properties of RE2,xMxCuO4 oxide sintering bulksELECTRONICS & COMMUNICATIONS IN JAPAN, Issue 12 2008Yusuke Ichino Abstract La2,xSrxCuO4 (LSCO) and Sm2,xCexCuO4 (SCCO) polycrystal bulks with x=0 to 0.10 were made by solid-phase reaction method. From the X-ray diffraction patterns, LSCO and SCCO were confirmed single phase. Seebeck coefficient, resistivity, and heat conductivity decreased with increasing amount of Sr2+ and Ce2+ substitution. We estimated ZT from these values and found that the highest value of ZT=0.034 at 323 K was achieved in the LSCO with x=0.02. As a result, we conclude that LSCO and SCCO showed high thermoelectric properties around room temperature. We can expect RE2,xMxCuO4 will be a very useful material for thermoelectric module operating at room temperature. © 2009 Wiley Periodicals, Inc. Electron Comm Jpn, 91(12): 24,28, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/ecj.10003 [source] Long-Lived Luminescent Dendrimers with a [Ru(dpp)3]2+ -Type Core: Synthesis and Photophysical PropertiesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 18 2009Uwe Hahn Abstract Metallodendrimers built around a [Ru(dpp)3]2+ -type core (dpp = 4,7-diphenyl-1,10-phenanthroline) were prepared containing peripheral phenyl moieties. The convergent synthesis of the ligands was accomplished by coupling dendritic branches with a focal amino function to the chelating phenanthroline precursor under the formation of sulfonamide linkages. Complexation of ruthenium ions afforded the corresponding metallodendrimers with up to 24 peripheral phenyl units in the case of the largest dendritic structure. The absorption spectra and luminescence properties of the four new dendrimers are reported. The dendritic effect is clearly visible, going from zero to second generation, as demonstrated by an elongation in the excited-state lifetime in aerated acetonitrile and improved emission quantum yields relative to the reference complex containing a [Ru(dpp)3]2+ core. Interestingly, the use of rigid and conjugated ruthenium-based cores results, for all dendritic structures, in luminescence lifetimes that are several microseconds long in deaerated solutions, even at room temperature.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Surfactant-Assisted Synthesis and Characterization of Novel Chain-Like CoNi Alloy AssembliesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 25 2007Lu-Ping Zhu Abstract Novel chain-like CoNi alloy assemblies with a length of up to 6,7 ,m were successfully prepared by a surfactant-assisted hydrothermal synthetic route at 100 °C for 2 h. The individual submicrospheres built from smaller CoNi nanoparticles had a diameter of about 400,500 nm. These microspheres were then integrated to form the novel chain-like CoNi alloy assemblies. The effects of synthetic parameters such as surfactant and solvent on the formation and morphology of CoNi samples were investigated. The experimental results showed that N2H4·H2O and CTA+ play important roles in the formation of the novel chain-like CoNi alloy assemblies. Based on the structural information provided by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, selected-area electron diffraction and energy-dispersive X-ray analysis, a growth mechanism was tentatively proposed for the formation of chain-like CoNi alloy assemblies. Magnetic hysteresis measurement revealed that the chain-like CoNi alloy assemblies display ferromagnetic behavior with a saturation magnetization of 96.15 emu/g and a coercivity of 144.75 Oe at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Nb-Doped VO2 Thin Films Prepared by Aerosol-Assisted Chemical Vapour DepositionEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 25 2007Clara Piccirillo Abstract Niobium-doped vanadium dioxide (VxNb1,xO2, x = 0,0.037) thin films were prepared by aerosol-assisted chemical vapour deposition (AACVD) of vanadyl(IV) acetonate and niobium(V) ethoxide in ethanol. Samples were analysed by EDX, XRD, Raman, XPS and SEM. The analyses confirmed the deposition of niobium, even if no separated phase was formed; the morphological structure of the films was affected by the dopant presence. The thin films showed thermochromic behaviour, with a marked change in optical properties above and below the switching temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Novel Cadmium(II) Adipate Coordination Polymers with Structural Transformation via Oxalate Ligand: Syntheses, Structures and Fluorescence PropertiesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 20 2004Na Hao Abstract Two novel cadmium adipate coordination polymers [Cd{O2C(CH2)4CO2}{1,10-phen}]n (1) and [Cd2(C2O4){O2C(CH2)4CO2(OH2)2}{2,2,-bipy}]·H2O (2) [adipic acid = HO2C(CH2)4CO2H] have been hydrothermally synthesized and characterized by elemental analyses, IR spectroscopy, thermogravimetric analysis and single-crystal X-ray diffraction. Crystallographic data for 1: monoclinic, C2/c, a = 16.186(3) Å, b = 15.487(3) Å, c = 14.052(3) Å, , = 112.73(3)°, Z = 8. Crystal data for 2: monoclinic, Cc, a = 23.448(5) Å, b = 11.826(2) Å, c = 8.3163(17) Å, , = 99.08(3)°, Z = 4. The structural analysis reveals that 1 forms a novel one-dimensional chain in which the binuclear Cd centers are linked by adipate anions. Compound 2 is the first example in which both a 2,2,-bipy ligand and an oxalate group are found in the {M/adipate} system. Compound 2 possesses one-dimensional sine- or cosine-type chains, which are alternately connected together by the oxalate group to form a three-dimensional framework. The structural determination reveals that the introduction of the oxalate ligand causes the dimensional transformation of the compounds. Compounds 1 and 2 show strong fluorescent properties at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] The Electronic Structure of (Diiminopyridine)cobalt(I) ComplexesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 6 2004Quinten Knijnenburg Abstract DFT calculations show that square-planar LCoIR complexes of a diiminopyridine ligand are best regarded as containing low-spin CoII antiferromagnetically coupled to a ligand radical anion. The lowest triplet state, corresponding to a 3d,,* excitation, is calculated to be only a few kcal/mol above the ground state, and is thermally accessible. The anomalous 1H NMR chemical shifts of the LCoR complexes are suggested to be due to thermal population of the triplet state at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] Synthesis, Crystal Structure, and Photoluminescent Properties of a Tetracarbonyl(naphthyridylcarbamoyl)rhenium(I) Complex and a Highly Emissive Tetracarbonyl(naphthyridylamido)rhenium(I) ComplexEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 2 2003Jing-Lin Zuo Abstract The reactions of Re(CO)5X (X = Cl, Br) with 7-amino-2,4-dimethyl-1,8-naphthyridine (H2L1) and 7-[2-(6-chloropyridyl)amino]-2,4-dimethyl-1,8-naphthyridine (HL2) in the presence of tBuOK afforded the ,1 -naphthyridylcarbamoyl complex [Re(CO)4(HL1CO)] (1) and the naphthyridylamido complex [Re(CO)4(L2)] (2), respectively. The structures of HL2, 1·CHCl3, 1·HL3·2CH2Cl2 [HL3 = (7-chloronaphthyridyl)(5,7-dimethylnaphthyridyl)amine], and 2 have been determined by X-ray crystallography. Complex 1 displays a weak emission at 453 nm in an EtOH/MeOH (1:4, v/v) glassy solution at 77 K; complex 2 exhibits an intense (quantum yield: 0.22 in CH2Cl2) and long-lived emission (46 ,s in CH2Cl2), with a solvent-sensitive ,max, in degassed solutions at room temperature. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2003) [source] Protonation of Diarylacetylenes in Superacid HSO3F and Their Oxidation in the HSO3F/PbO2 System: One-Pot Synthesis of Polysubstituted NaphthalenesEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 27 2008Aleksander V. Vasilyev Abstract In the superacid HSO3F, diarylacetylenes bearing one electron-withdrawing group (NO2, CN, COMe, CO2Me) in each arene ring form stable ions, protonated at these groups. Oxidation of such diarylacetylenes in the HSO3F/PbO2 system at ,75 to ,50 °C over 2,2.5 h, followed by quenching of the reaction mixture with hydrochloric (or hydrobromic) acid at ,60 to 25 °C, resulted in the formation of (E,E)-1,4-dichloro (or dibromo)-1,2,3,4-tetraarylbuta-1,3-dienes. These butadienes spontaneously undergo electrocyclic transformation into polysubstituted naphthalenes at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] A New Approach to the Synthesis of N,N -Dialkyladenine DerivativesEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 29 2007M. José Alves Abstract N,N- Dialkyladenine derivatives were prepared by two different reaction sequences starting from 5-amino-4-cyanoformimidoylimidazoles. When these imidazoles were treated with dimethylformamide diethyl acetal, a 5-aminomethyleneamino-4-cyanoformimidoylimidazole was isolated and evolved to the N,N- dialkyladenine in the presence of a secondary alkylamine. The same purine structure was isolated when the 5-amino-4-cyanoformimidoylimidazole was first treated with a secondary amine to give a stable 4-amidino-5-aminoimidazole. The desired product was generated when the 4-amidino-5-aminoimidazole was combined with dimethylformamide diethyl acetal, at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] N -Functionalization of Azoles through Coupling Reactions with Alkoxydienyl and Alkoxystyryl Boronic EstersEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 8 2007Annamaria Deagostino Abstract Alkoxydienyl boronates 1a and 1b and alkoxystyryl boronate 2 have been used in various copper mediated cross-coupling reactions with azoles. A variety of N -alkoxydienyl- and N -styrylazoles have been synthesized under mild conditions. The process utilizes Cu(OAc)2 in the presence of CsF in CH2Cl2 at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Lithium Perchlorate-Catalyzed Three-Component Coupling: A Facile and General Method for the Synthesis of ,-Aminophosphonates under Solvent-Free ConditionsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 23 2003Najmedin Azizi Abstract A simple, efficient, and general method has been developed for the synthesis of ,-aminophosphonates in the presence of solid lithium perchlorate under solvent-free conditions. Thus secondary and tertiary ,-aminophosphonates were synthesized relatively quickly in good yields at room temperature. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003) [source] Research on the human thermal model with a poly-segmented handHEAT TRANSFER - ASIAN RESEARCH (FORMERLY HEAT TRANSFER-JAPANESE RESEARCH), Issue 2 2008Ding Li Abstract A more integral human thermal model was built by combining the human thermal cylindrical model and the manual poly-segment thermal model. Finite element methods (FEM) was used to define the body thermal model. It was in good agreement with the experimental results. The results show: the experimental results are consistent with the calculated value, when suitable blood flux is taken into consideration. The blood flux is in a certain range when the manual temperature is stable. Blood flux is the major factor in the manual temperature field. Body temperature and intake artery temperature have little effect on the hand temperature. © 2008 Wiley Periodicals, Inc. Heat Trans Asian Res, 37(2): 94,100, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/htj.20187 [source] A basic study on humidity recovery by using micro-porous media (Effects of thermal condition of fluids and geometrical condition of apparatus on transport performance)HEAT TRANSFER - ASIAN RESEARCH (FORMERLY HEAT TRANSFER-JAPANESE RESEARCH), Issue 8 2006Shixue Wang Abstract Using an experimental apparatus to examine the performance of heat and mass transfer between constant-temperature water and dry air through a porous plate having extremely small pores, the effects of the thermal conditions in the fluids and the geometric condition of the apparatus on moisture transport were measured. The effects of water temperature, thickness of the porous plate, and channel height of the flowing air on moisture transport are noticeable. However, the effect of air temperature in the channel inlet on moisture transport is slight. In addition, in order to evaluate the degree of air humidity absorption, a parameter called the moisture absorption rate was introduced. The moisture absorption rate was shown to decrease with increasing air velocity and varies only slightly for a plate thickness of 1 mm and decreases for a plate thickness of 3.5 mm with increasing water temperature. © 2006 Wiley Periodicals, Inc. Heat Trans Asian Res, 35(8): 568,581, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/htj.20133 [source] A modified and green methodology for preparation of polysubstituted furansHETEROATOM CHEMISTRY, Issue 4 2005Javad Azizian In this study, we introduced a very simple, one-pot and green methodology for preparation of polysubstituted furans by reaction of aromatic aldehydes, DMAD, and alkylisocyanides in water and at room temperature. © 2005 Wiley Periodicals, Inc. 16:259,262, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20086 [source] Shock tube study of 1,3,5-triazine dissociation and relaxation and relaxation of pyrazineINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 4 2010Hui Xu The three-body dissociation of 1,3,5-triazine (s-triazine, s-C3H3N3 , 3HCN) has been observed in incident shock waves with the laser-schlieren technique. The experiments use 5% triazine/Kr and cover 1630,2350 K for 100,600 Torr. These experiments show dissociation rates with strong falloff and a slight but fully expected pressure dependence. The dissociation is without secondary reaction save for a possible, but rather unlikely, contribution from the isomerization HCN , HNC. Electronic structure calculations of the transition-state properties (G3B3, HL1, Eo = 84.6 kcal/mol) are used to construct a Rice,Ramsperger,Kassel,Marcus (RRKM) model whose fit to the rate measurements suggests a ,,E,down of 1200 cm,1. However, a seemingly better fit is achieved using the barrier of 81 kcal/mol proposed by Dyakov et al. (J. Phys. Chem. A 2007, 111, 9591,9599). With this barrier k, (s,1) = 5.3 × 1016 exp(,86.6(kcal/mol)/RT), and the fit now accepts the more routine ,,E,down = 126(T/298)0.9. It seems the dissociation most likely occurs by a direct, one-step, "triple" dissociation to 3HCN, although the present experiments cannot rule out a multistep process. Vibrational relaxation of the triazine was also examined in 5% and 20% mixtures with Kr over 770,1500 K for pressures between 6 and 14 Torr. Relaxation is very fast, with a slight inverse temperature dependence, P, rising from 100 to 200 ns-atm over the full temperature range. Integrated gradients are in good accord with calculated total changes in density, indicating a single exponential relaxation. A separate investigation of relaxation in the related molecule pyrazine (500,1300 K, in 1% and 5% in Kr, between 13 and 66 Torr) is included. Again relaxation is rapid, but here the temperature dependence seems more normal, the relaxation times decreasing slightly with temperature. © 2010 Wiley Periodicals, Inc. Int J Chem Kinet 42: 211,220, 2010 [source] The complexity of formulating diets for zoo animals: a matrixINTERNATIONAL ZOO YEARBOOK, Issue 1 2005S. Crissey The nutrition matrix presented here identifies a variety of factors that need to be considered when formulating diets for wild animals in captivity. The matrix is designed to be adapted so that it can be customized as required. Food consumption, nutritional requirements, health status and management constraints and opportunities are the four main categories to focus on when developing diets. Each of these categories may, in turn, be affected by other factors. (1) Food consumption is affected by the diet offered, client (zoo animal manager, keeper or veterinarian) wishes and animal preferences. (2) Nutritional requirements are defined by known species requirements and National Research Council recommendations, morphology and feeding ecology. Nutritional requirements may also be influenced by season, life-stage, activity, health status, stress and body temperature. (3) Health status can be affected by nutritional deficiencies or toxicities in the diet offered. Certain health conditions may require specific dietary input. (4) Animal-management protocols, such as housing, breeding opportunities and environment, are affected by other animals, food storage and preparation capacity, and feeding regime, which, in turn, can be affected by training, exercise and enrichment. [source] Synthesis, characterization, and comparison of properties of novel fluorinated poly(imide siloxane) copolymersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Anindita Ghosh Abstract Four new poly(imide siloxane) copolymers were prepared by a one-pot solution imidization method at a reaction temperature of 180°C in ortho -dichlorobenzene as a solvent. The polymers were made through the reaction of o -diphthaleic anhydride with four different diamines,4,4,-bis(p -aminophenoxy-3,3,-trifluoromethyl) terphenyl, 4,4,-bis(3,-trifluoromethyl- p -aminobiphenyl ether)biphenyl, 2,6-bis(3,-trifluoromethyl- p -aminobiphenyl ether)pyridine, and 2,5-bis(3,-trifluoromethyl- p -aminobiphenylether)thiopene,and aminopropyl-terminated poly dimethylsiloxane as a comonomer. The polymers were named 1a, 1b, 1c, and 1d, respectively. The synthesized polymers showed good solubility in different organic solvents. The resulting polymers were well characterized with gel permeation chromatography, IR, and NMR techniques. 1H-NMR indicated that the siloxane loading was about 36%, although 40 wt % was attempted. 29Si-NMR confirmed that the low siloxane incorporation was due to a disproportionation reaction of the siloxane chain that resulted in a lowering of the siloxane block length. The films of these polymers showed low water absorption of 0.02% and a low dielectric constant of 2.38 at 1 MHz. These polyimides showed good thermal stability with decomposition temperatures (5% weight loss) up to 460°C in nitrogen. Transparent, thin films of these poly(imide siloxane)s exhibited tensile strengths up to 30 MPa and elongations at break up to 103%, which depended on the structure of the repeating unit. The rheological properties showed ease of processability for these polymers with no change in the melt viscosity with the temperature. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Functional properties of thermoformed wheat gluten/montmorillonite materials with respect to formulation and processing conditionsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008Hélène Angellier-Coussy Abstract Wheat gluten (WG)/montmorillonite (MMT) films were prepared by a thermomechanical process consisting of first mixing the components in a two-blade, counter-rotating device and second thermoforming the obtained dough. A significant loss in protein solubility due to the formation and rearrangement of disulfide bonds was observed upon mixing and thermoforming. In the range of studied glycerol contents (25,42.8 wt %), it was shown that glycerol had no significant effect on the mechanical properties or water sensitivity of WG-based films. Increasing the thermoforming temperature from 60 to 120°C led to considerable improvements of the mechanical properties (increases in both the stress and strain at break) and a significant reduction of the water sensitivity. The introduction of MMT (up to 5 wt %) allowed the achievement of mechanical properties that were not possible by just the variation of the glycerol content and the processing temperature. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Thermal analysis of polymer,water interactions and their relation to gas hydrate inhibitionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007Manika Varma-Nair Abstract Gas hydrates formed in oil production pipelines are crystalline solids where hydrocarbon gas molecules such as methane, propane, and their mixtures are trapped in a cagelike structure by hydrogen-bonded water molecules to form undesirable plugs. Methanol and glycol are currently used to prevent these plugs via thermodynamic inhibition. Small amounts of water-soluble polymers may provide an alternate approach for preventing gas hydrates. In this study, we expand the fundamental understanding of water,polymer systems with differential scanning calorimetry. Nonfreezable bound water was used to quantify polymer,water interactions and relate them to the chemical structure for a series of polymers, including acrylamides, cyclic lactams, and n -vinyl amides. For good interactions, the water structure needs to be stabilized through hydrophobic interactions. An increased hydrophobicity of the pendant group also appears to favor polymer performance as a gas hydrate inhibitor. Good inhibitors, such as poly(diethyl acrylamide) and poly(N -vinyl caprolactam), also show higher heat capacities, which indicate higher hydrophobicity, than poor performers such as polyzwitterions, in which hydrophilicity dominated. The phase behavior and thermodynamic properties of dilute polymer solutions were also evaluated through measurements of the heat of demixing and lower critical solution temperature. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2642,2653, 2007 [source] Time-dependent quantum study of H(2S) + FO(2,) , OH(2,) + F(2P) reaction on the 13A, and 13A, statesJOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 14 2010Fahrettin Gogtas Abstract The dynamics of the H(2S) + FO(2,) , OH(2,) + F(2P) reaction on the adiabatic potential energy surface of the 13A, and 13A, states is investigated. The initial state selected reaction probabilities for total angular momentum J = 0 have been calculated by using the quantum mechanical real wave packet method. The integral cross sections and initial state selected reaction rate constants have been obtained from the corresponding J = 0 reaction probabilities by means of the simple J -Shifting technique. The initial state-selected reaction probabilities and reaction cross section do not manifest any sharp oscillations and the initial state selected reaction rate constants are sensitive to the temperature. © 2010 Wiley Periodicals, Inc. J Comput Chem 2010 [source] MOISTURE SORPTION CHARACTERISTICS of STARCH GELS.JOURNAL OF FOOD PROCESS ENGINEERING, Issue 3 2004PART II: THERMODYNAMIC PROPERTIES ABSTRACT A thermodynamic approach was used to interpret the experimental adsorption and desorption isotherm data for potato starch gel. Calculation of the thermodynamic properties (differential enthalpy, integral enthalpy, differential entropy and integral entropy) provides an understanding of the properties of water and energy requirements associated with the sorption behavior. Isosteric heats (differential enthalpies) were calculated through direct use of moisture isotherms by applying the Clausius-Clapeyron equation. the differential enthalpy and entropy decreased with increasing moisture content and were adequately characterized by an exponential model. A plot of differential heat versus entropy satisfied the enthalpy-entropy compensation theory. the spreading pressure increased with increasing water activity, and decreased with increasing temperature. the net integral enthalpy increased with moisture content to a maximum value (around the monolayer moisture content) and then decreased. In a reverse manner, the net integral entropy decreased with moisture content to a minimum value and then increased. [source] JOURNAL of FOOD PROCESSING and PRESERVATION SEP 2000 Vol-24.4. DEVELOPMENT of A PROCESS FOR DETECTING NONTHERMAL EFFECTS of MICROWAVE ENERGY ON MICROORGANISMS AT LOW TEMPERATURE,JOURNAL OF FOOD PROCESSING AND PRESERVATION, Issue 4 2000MICHAEL KOZEMPEL We developed an experimental process capable of isolating thermal and nonthermal effects of microwave energy relative to the destruction of microorganisms at low temperature. the concept combines instantaneous energy input to the food system by microwaves with rapid removal of thermal energy. the process used a double tube heat exchanger inside a continuous microwave dryer. the outer tube was transparent to microwaves, whereas the inner tube was stainless steel and was used for cooling the system. the microwave energy, 5,6 kW power, was absorbed by the process fluid in the annulus. the cooling water flowing in the inner tube removed the thermal energy from the process fluid to control temperature at or below 45C. the process was at turbulent flow to assure a uniform temperature and dwell time. There were no detected nonthermal effects from microwave energy for yeast, Pediococcus sp., Escherichia coli, Listeria innocua, or Enterobacter aerogenes in various test fluids, such as water, liquid egg, beer, apple juice, apple cider, and tomato juice. [source] Ethyl-paraben and nicotinamide mixtures: Apparent solubility, thermal behavior and X-ray structure of the 1:1 co-crystal,JOURNAL OF PHARMACEUTICAL SCIENCES, Issue 11 2008S. Nicoli Abstract This work aims at investigating the nicotinamide (NA),ethyl-paraben (EP) binary system both in solution and in the solid state. In particular, the apparent EP solubility in water was studied in the presence of different NA concentrations (between 0.28 and 1.64 M). It was found that the apparent EP solubility increase (nearly twofold) observed at the highest NA concentration tested can be ascribed to a change in the polarity of the solvent mixture, rather than to a direct effect of NA on EP. The effect of fusion and re-crystallization from water or ethanol solutions on EP and NA mixtures was investigated by means of differential scanning calorimetry, elemental analysis and X-ray diffraction both on powder and single crystal. It was discovered that EP and NA form a co-crystal having a 1:1 molar composition that can be easily crystallized from ethanol. Single crystal X-ray analysis of this species revealed that the NA and EP molecules form corrugated layers within which the two components are intimately associated by a dense network of hydrogen bonds. In the presence of an excess NA in solution, the EP-NA co-crystal has lower water solubility with respect to both the single co-crystal formers and precipitates in aqueous solutions at ambient temperature. © 2008 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 97:4830,4839, 2008 [source] Polymorph transitions of bicalutamide: A remarkable example of mechanical activationJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 8 2008Zoltán Német Abstract Bicalutamide, an active pharmaceutical ingredient possessing antiandrogenic activity, is known to exhibit polymorphism. The higher melting Form I relates monotropically to the lower melting Form II. The amorphous form can be easily produced by quench cooling the melt, but it is known to crystallize spontaneously to Form II at room temperature within days. Our results show that crystallization of amorphous bicalutamide is greatly influenced by experimental conditions and sample treatment. The effect of mechanical activation on the polymorph transitions is investigated in detail. Seeds of Form I can be formed in the amorphous phase even due to gentle mechanical treatment, which results in crystallization to the more stable structure at elevated temperature. The crystalline Form II may as well be transformed to the stable modification through mechanical activation at elevated temperature. © 2007 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 97: 3222,3232, 2008 [source] Room-temperature RAFT copolymerization of 2-chloroallyl azide with methyl acrylate and versatile applications of the azide copolymersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 6 2010Guang Li Abstract A new vinyl azide monomer, 2-chlorallyl azide (CAA), has been synthesized from commercially available reagent in one step. The reversible addition fragmentation chain transfer (RAFT) copolymerization of CAA with methyl acrylate (MA) was carried out at room temperature using a redox initiator, benzoyl peroxide (BPO)/N,N -dimethylaniline (DMA), in the presence of benzyl 1H -imidazole-1-carbodithioate (BICDT). The polymerization results showed that the process bears the characteristics of controlled/living radical polymerizations, such as the molecular weight increasing linearly with the monomer conversion, the molecular weight distribution being narrow, and a linear relationship existing between ln([M]0/[M]) and the polymerization time. Chain extension polymerization was performed successfully to prepare block copolymer. Furthermore, the azide copolymers were functionalized by CuI -catalyzed "click" reaction with alkyne-containing poly(ethylene glycol) (PEG) to yield graft copolymers with hydrophilic PEG side chains. Surface modification of the glass sheet was successfully achieved via the crosslinking reaction of the azide copolymer under UV irradiation at ambient temperature. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1348,1356, 2010 [source] | ||||||||||||||||||||||