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Melting Point (melting + point)
Kinds of Melting Point Selected AbstractsThe Fluid-Mosaic Model, Homeoviscous Adaptation, and Ionic Liquids: Dramatic Lowering of the Melting Point by Side-Chain Unsaturation,ANGEWANDTE CHEMIE, Issue 15 2010Samuel Unerwartet: Ionische Flüssigkeiten mit langen ungesättigten Alkylresten (obere Struktur) trotzen den gängigen Trends, nach denen lange ionengebundene Alkylgruppen höhere Schmelzpunkte bedeuten, und sind weniger viskos als ein gesättigter Standard (untere Struktur) bei derselben Temperatur. Diese Merkmale ähneln denjenigen bei der Viskositätsanpassung der Zellmembran in manchen Organismen und sprechen für einen Flüssig-Mosaik-Charakter im Nanomaßstab. [source] Estimation of the ideal solubility (crystal,liquid fugacity ratio) of organic compoundsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 3 2010Samuel H. Yalkowsky Abstract Melting point, entropy of melting and heat capacity of melting are required for the calculation of the ideal solubility of a solid solute via the Clausius,Clapyron equation. This article reviews the published approximations of estimating entropy and heat capacity of melting. By comparing the available experimental results to calculated values the authors attempt to identify the best estimation of the ideal solubility and crystal,liquid fugacity ratio for organic compounds. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 1100,1106, 2010 [source] Effect of characteristics of compounds on maintenance of an amorphous state in solid dispersion with crospovidoneJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 6 2007Yusuke Shibata Abstract Solid dispersion (SD) of indomethacin with crospovidone (CrosPVP) shows useful characteristics for preparation of dosage forms. This study aimed to determine the types of drugs that could adopt a stable amorphous form in SD. Twenty compounds with various melting points (70,218°C), molecular weights (135,504) and functional groups (amide, amino, carbonyl, hydroxyl, ketone etc.) were prepared in SD with CrosPVP. The CrosPVP SDs were prepared using a mechanical mixing and heating method. Melting point and molecular weight were found to have no influence on the ability of a compound to maintain an amorphous state in SD. All compounds containing hydrogen-bond-donor functional groups existed in an amorphous state in SD for at least 6 months. Infrared spectra suggested an interaction between the functional groups of these compounds and amide carbonyl group of CrosPVP. Compounds without hydrogen-bond-donor groups could not maintain an amorphous state and underwent recrystallization within 1 month. It was suggested that the presence of a hydrogen-bond-donor functional group in a compound is an important factor affecting the stable formation of SD with CrosPVP, which contains a hydrogen-bond acceptor. © 2006 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 96:1537,1547, 2007 [source] Preparation of ZnO thin films by MO-CVD method using bis(acetylacetonato) zinc(II) anhydrate fiberPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 6 2010Shigeyuki Seki Abstract The MO-CVD method as a deposition process corresponding to the mass production of the high-quality ZnO film that can be used as an active layer in the thin film transistor is paid to attention. Bis(acetylacetonato) zinc(II) (Zn(acac)2) which has chemical stability and low toxicity is promising as the inexpensive raw material for CVD. The problem includes (1) pollution with water in process by character to easily take water of crystallization, and (2) the supply of the gas-phase raw material by sublimation should be not able to be controlled easily because it is a fine particle. In this study, Zn(acac)2 anhydrate fiber was prepared from Zn(acac)2 monohydrate powder by the sublimation process. Melting point of this fiber was almost same (,134 °C) as the monohydrate powder in N2 atmosphere. ZnO film was deposited on r-face sapphire substrate by MO-CVD process using Zn(acac)2 anhydrate fiber, successfully. RMS of the film flatness was 0.48 nm. This film had resistivity of 4.6 × 10,1 ,·cm, carrier electron density of 9.1 × 1017 cm,3 and Hall mobility of 15 cm2·V,1·s,1. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Preparation and evaluation of composite electromagnetic wave absorbers made of aluminum fine particles dispersed in polystyrene mediumELECTRONICS & COMMUNICATIONS IN JAPAN, Issue 1 2010Norizumi Asano Abstract We developed composite electromagnetic wave absorbers consisting of dispersed aluminum fine particles in a polystyrene medium and evaluated their properties in order to realize single-layer electromagnetic wave absorbers with good absorption in the gigahertz region. Polystyrene particles with two diameters (approximately 200 ,m and 1 ,m) and fine aluminum particles were mixed by mechanical milling. The mixture was heated above the melting point of polystyrene and then cooled naturally in air. The frequency characteristics of the complex relative permeability and the complex relative permittivity were calculated from the values of the scattering parameters of a coaxial line loaded with a sample of a toroidal-core shape. Both the diamagnetism and the magnetic loss increased in proportion to the volume mixing ratios of aluminum particles up to approximately 34 vol for samples made of polystyrene particles with approximately 200 ,m or 1,m diameter. The diamagnetism was almost frequency-independent and the magnetic loss decreased with increasing frequency for all samples. These results were in agreement with qualitative theoretical prediction. © 2009 Wiley Periodicals, Inc. Electron Comm Jpn, 93(1): 30, 40, 2010; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/ecj.10169 [source] Acute toxicity of fatty acids to the freshwater green alga Selenastrum capricornutumENVIRONMENTAL TOXICOLOGY, Issue 5 2003Yasushi Kamaya Abstract The acute toxicity of fatty acids (C14 to C18) commonly found in wood was determined by the standard algal growth inhibition test using the freshwater green alga Selenastrum capricornutum. Toxicity, quantified as IC50 values, varied depending on the number of total carbons and double bonds. Of the tested acids, oleic (cis -9-octadecenoic) acid showed the highest toxicity (72-h IC50 = 0.47 mg/L) to the alga, and triolein, a triglyceride of oleic acid, showed no apparent toxicity. Further examination of a series of C18:1 acids with a double bond at the 6, 11, or 12 position revealed that both double-bond position and cis or trans configuration affected toxicity. The 72-h IC50 data for these fatty acids and related compounds seemed to correlate well with the melting point (mp), showing two separate linear relationships: at mp < 35°C toxicity increased with increasing melting point, and at mp > 40°C toxicity decreased with melting point. © 2003 Wiley Periodicals, Inc. Environ Toxicol 18: 289,294, 2003. [source] Determination of physicochemical properties of tetrabromobisphenol AENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2008Hidetoshi Kuramochi Abstract Aqueous solubility (Sw), 1-octanol/water partition coefficient (KOW), and vapor pressure of the nonionic form of 2,2,,6,6,-tetrabromo-4,4,-isopropylidenediphenol (tetrabromobisphenol A or TBBP-A) were measured. From this, enthalpies of solution and vaporization were estimated. Furthermore, enthalpy of fusion and melting point were measured to estimate subcooled liquid vapor pressure, the infinite dilution activity coefficient, and Henry's law constant. Since TBBP-A is expected to exit in both ionic and nonionic forms at near neutral pH, pH effects on physicochemical properties were also examined. Because of the ionization of TBBP-A, Sw increased by five orders of magnitude, while KOW decreased by eight orders of magnitude. Furthermore, an analytical model based on mass balance and dissociation of TBBP-A was applied to represent the pH dependence. [source] Extraction, purification and characterization of wax from flax (Linum usitatissimum) strawEUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, Issue 7 2009Yasantha Athukorala Abstract The chemical composition and selected physical parameters of wax extracted from flax straw with supercritical CO2 (SC-CO2) and hexane have been determined. From the GC/MS results, clear variations in composition and component distributions were observed between SC-CO2 - and hexane-extracted samples. The major components of the SC-CO2 and hexane extracts from three flax cultivars were: fatty acids (36,49%), fatty alcohols (20,26%), aldehydes (10,14%), wax esters (5,12%), sterols (7,9%) and alkanes (4,5%). Purification of SC-CO2 -extracted wax with silica gel chromatography yielded 0.4,0.5% (dry matter) and was composed primarily of wax esters (C44, C46 and C48) and alkanes (C27, C29 and C31). UV-Vis scans of the purified wax samples exhibited two main peaks indicating the presence of conjugated dienes and carotenoids or related compounds. Fourier transform infrared results showed prominent peaks at 2918 (-C-H), 2849 (-C-H), 1745 (-C=O), 1462 (-C-H), 1169 (-C-O) and 719,cm,1 (-(CH2)n -), with NorLin wax showing a slightly deviating pattern compared to the other samples. Thermal analysis by differential scanning calorimetry revealed a mean melting point of 55,56,°C and oxidation temperatures of 146,153,°C for purified wax from flax straw processed using different procedures. [source] Effects of hydrogenation parameters on trans isomer formation, selectivity and melting properties of fatEUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, Issue 3 2008Anar Musavi Abstract Effects of hydrogenation conditions (temperature, hydrogen pressure, stirring rate) on trans fatty acid formation, selectivity and melting behavior of fat were investigated. To this aim, soybean oil was hydrogenated under various conditions and fatty acid composition, trans isomer formation, slip melting point (SMP), solid fat content (SFC) and iodine number (IV) of the samples withdrawn at certain intervals of the reactions were monitored. A constant ratio (0.03%) of Nysosel 222 was used in the various combinations of temperature (150, 165 and 180,°C), stirring speed (500, 750 and 1000,rpm) and hydrogen pressure (1, 2 and 3,bar). Raising the temperature increased the formation of fatty acid isomers, whereas higher stirring rates decreased this formation, while changes in hydrogen pressure had no effect or slightly reduced it, depending on other parameters. Results also indicated that the trans fatty acid ratio increased with IV reduction, reached the highest value when the IV was about 70 and decreased at IV < 70 due to saturation. Selectivity values (S21) at that point ranged between 5.78 and 11.59. Lower temperatures and higher stirring rates decreased not only the trans isomer content but also the S21 values at significant levels. However, same effects were not observed with the changes in hydrogen pressure. It was determined that a high SMP does not necessarily mean a high SFC. Selective conditions produced samples with higher SFC but lower SMP, which is possibly because of higher trans isomer formation as well as lower saturation. [source] Microstructure and Properties of SiC Honeycomb StructuresADVANCED ENGINEERING MATERIALS, Issue 12 2008D. Galsterer In this work, a novel processing route was used for fabrication of porous beta-SiC materials below 1450,°C. Honeycomb structures, based on Si, C and Al, were extruded and afterwards converted into SiC based ceramics at temperatures between 1050,°C and 1450,°C in Ar atmosphere. A conversion temperature below 1450,°C was applied due to the low melting point of the used Si-Al-alloy. [source] Developmental and environmental regulation of antifreeze proteins in the mealworm beetle Tenebrio molitorFEBS JOURNAL, Issue 21 2000Laurie A. Graham The yellow mealworm beetle, Tenebrio molitor, contains a family of small Cys-rich and Thr-rich thermal hysteresis proteins that depress the hemolymph freezing point below the melting point by as much as 5.5 °C (,T = thermal hysteresis). Thermal hysteresis protein expression was evaluated throughout development and after exposure to altered environmental conditions. Under favorable growth conditions, small larvae (11,13 mg) had only low levels of thermal hysteresis proteins or thermal hysteresis protein message, but these levels increased 10-fold and 18-fold, respectively, by the final larval instar (> 190 mg), resulting in thermal hysteresis >,3 °C. Exposure of small larvae (11,13 mg) to 4 weeks of cold (4 °C) caused an ,,20-fold increase in thermal hysteresis protein concentration, well in excess of the less than threefold developmental increase seen after 4 weeks at 22 °C. Exposure of large larvae (100,120 mg) to cold caused 12-fold and sixfold increases in thermal hysteresis protein message and protein levels, respectively, approximately double the maximum levels they would have attained in the final larval instar at 22 °C. Thus, thermal hysteresis increased to similar levels (> 4 °C) in the cold, irrespective of the size of the larvae (the overwintering stage). At pupation, thermal hysteresis protein message levels decreased >,20-fold and remained low thereafter, but thermal hysteresis activity decreased much more slowly. Exposure to cold did not reverse this decline. Desiccation or starvation of larvae had comparable effects to cold exposure, but surprisingly, short daylength photoperiod or total darkness had no effect on either thermal hysteresis or message levels. As all environmental conditions that caused increased thermal hysteresis also inhibited growth, we postulate that developmental arrest is a primary factor in the regulation of T. molitor thermal hysteresis proteins. [source] Advances in modelling heat transfer through wood framed walls in fireFIRE AND MATERIALS, Issue 6 2001P. Clancy Described in this paper are advances made in modelling heat transfer through wood framed walls in fire. Previously unpublished experimental results are also given. This type of modelling is used for the determination of the performance of fire safety systems, such as wood framed wall barriers, in accordance with new performance-based building regulations being introduced around the world. Advances include a discrete modelling method for radiative heat transfer in cavities with re-entrant corners and gaps formed by the shrinkage of stud cross-sections. It has been shown that the formation of the gaps can prevent temperatures rising in the fire side of studs by as much as 100,200°C. A simple means of modelling heat transfer by the movement of moisture and vapour, involving the modification of conductivity values has been developed. Sloughing of gypsum board sheets has been satisfactorily modelled assuming that a sheet sloughs when the temperature on the surface opposite the fire reaches the melting point of glass fibres in the gypsum board; that is, approximately 700°C. Recommendations on thermal properties obtained independently by other researchers are presented. Overall, the advances improve temperature predictions and broaden the range of walls that can be modelled including staggered stud walls as well as ordinary cavity walls. Copyright © 2002 John Wiley & Sons, Ltd. [source] Enhanced Thermal Stability and Efficiency of Polymer Bulk-Heterojunction Solar Cells by Low-Temperature Drying of the Active LayerADVANCED FUNCTIONAL MATERIALS, Issue 5 2010Ching Lin Abstract This study addresses two key issues, stability and efficiency, of polymer solar cells based on blended poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) by demonstrating a film-forming process that involves low-temperature drying (,5,°C) and subsequent annealing of the active layer. The low-temperature process achieves 4.70% power conversion efficiency (PCE) and ,1250,h storage half-life at 65,°C, which are significant improvements over the 3.39% PCE and ,143,h half-life of the regular room-temperature process. The improvements are attributed to the enhanced nucleation of P3HT crystallites as well as the minimized separation of the P3HT and PCBM phases at the low drying temperature, which upon post-drying annealing results in a morphology consisting of small PCBM-rich domains interspersed within a densely interconnected P3HT crystal network. This morphology provides ample bulk-heterojunction area for charge generation while allowing for facile charge transport; moreover, the P3HT crystal network serves as an immobile frame at heating temperatures less than the melting point (Tm) of P3HT, thus preventing PCBM/P3HT phase separation and the corresponding device degradation. [source] A thermochemical boundary layer at the base of Earth's outer core and independent estimate of core heat fluxGEOPHYSICAL JOURNAL INTERNATIONAL, Issue 3 2008David Gubbins SUMMARY Recent seismological observations suggest the existence of a ,150-km-thick density-stratified layer with a P -wave velocity gradient that differs slightly from PREM. Such a structure can only be caused by a compositional gradient, effects of a slurry or temperature being too small and probably the wrong sign. We propose a stably stratified, variable concentration layer on the liquidus. Heat is transported by conduction down the liquidus while the light and heavy components migrate through the layer by a process akin to zone refining, similar to the one originally proposed by Braginsky. The layer remains static in a frame of reference moving upwards with the expanding inner core boundary. We determine the gradient using estimates of co, the concentration in the main body of the outer core, and cb, the concentration of the liquid at the inner core boundary. We determine the depression of the melting point and concentrations using ideal solution theory and seismologically determined density jumps at the inner core boundary. We suppose that co determines ,,mod, the jump from normal mode eigenfrequencies that have long resolution lengths straddling the entire layer, and that cb determines ,,bod, the jump determined from body waves, which have fine resolution. A simple calculation then yields the seismic, temperature, and concentration profiles within the layer. Comparison with the distance to the C-cusp of PKP and normal mode eigenfrequencies constrain the model. We explore a wide range of possible input parameters; many fail to predict sensible seismic properties and heat fluxes. A model with ,,mod= 0.8 gm cc,1, ,,bod= 0.6 gm cc,1, and layer thickness 200 km is consistent with the seismic observations and can power the geodynamo with a reasonable inner core heat flux of ,2 TW and nominal inner core age of ,1 Ga. It is quite remarkable and encouraging that a model based on direct seismic observations and simple chemistry can predict heat fluxes that are comparable with those derived from recent core thermal history calculations. The model also provides plausible explanations of the observed seismic layer and accounts for the discrepancy between estimates of the inner core density jumps derived from body waves and normal modes. [source] Formation and Properties of Responsive Siloxane-Based Polymeric Surfaces with Tunable Surface Reconstruction KineticsADVANCED FUNCTIONAL MATERIALS, Issue 3 2009Julie Ann Crowe-Willoughby Abstract Here, the formation of responsive polymeric materials with tunable response time is reported. These structures are fabricated by chemically modifying poly(vinylmethyl siloxane) (PVMS) networks with alkanethiols bearing a hydrophilic end-group (COOH or OH). The response time is facilitated by the liquid nature of the PVMS backbone and increases with increase in length of the methylene spacer (CH2)n in the alkanethiol pendent group. While for n,=,2 and 6, the surface reconstructs almost instantaneously, specimens with n,=,11 resist reconstruction because of strong van der Waals forces, leading to the formation of semi-crystalline regions. It is demonstrated that the responsive nature of PVMSS(CH2)11OH can be fine-tuned by varying the temperature; it possesses a faster response at temperatures above the melting point of the S(CH2)11OH moiety. [source] Fabrication of Microcantilever Sensors Actuated by Piezoelectric Pb(Zr0.52Ti0.48)O3 Thick Films and Determination of Their Electromechanical Characteristics,ADVANCED FUNCTIONAL MATERIALS, Issue 12 2005H. Park Abstract The integration and the device realization of Pb(Zr,,Ti)O3 (PZT) thick films on Si substrates are known to be extremely difficult because the processing temperature of the PZT thick film is close to the melting point of Si. However, PZT thick-film devices on Si warrant attention as they are appropriate for biological transducers; they generate large actuating forces and have a relatively high sensitivity for mass detection, especially in liquids. In this study, Pb(Zr0.52Ti0.48)O3 thick-film cantilever devices are successfully fabricated on a Pt/TiO2/SiNx/Si substrate using a screen-printing method and microelectromechanical systems (MEMS) process. Elastic and electromechanical properties such as the Young's modulus and transverse piezoelectric coefficient are determined from microstructural and electrical analyses for further mechanical study. The calculated Young's modulus of the thick film, 53.9,±,3.85,GPa, corresponds to the resonant frequency obtained from the measured harmonic oscillation response. The transverse piezoelectric constant, d31, of ,20.7 to ,18.8,pC,N,1 is comparable to that of a dense thin film. These values promise the possibility of determining the resonance properties of a thick-film cantilever by designing its structure and then simulating the harmonic oscillation response. Using the PZT thick-film cantilever, a strong harmonic oscillation with a quality (Q) factor of about 23 is demonstrated in water. The observation of strong harmonic oscillation in liquid implies the feasibility of precise real-time recognition of biomolecules using PZT thick-film cantilevers. [source] Numerical simulation of thermal runaway phenomena in silicon semiconductor devicesHEAT TRANSFER - ASIAN RESEARCH (FORMERLY HEAT TRANSFER-JAPANESE RESEARCH), Issue 6 2002Kazanori Shioda Abstract A mathematical model for heat production due to thermal excitation of conductive electrons and positive holes in a semiconductor pn junction is derived and discussed. The model is applied to simulate the thermal runaway phenomena in power electronics semiconductor devices. Our discussion focuses especially on the modeling of unexpected huge currents due to an excessive temperature increase. Calculated dynamics of temperature distributions of a silicon wafer while cooling performance decreases proved it is possible for a silicon wafer to be heated over its melting point in a few milliseconds. Our results indicate that if a local hot spot arises in a wafer, the thermal intrinsic excitation carries an increased diffusion current of minor carriers and a recombination current in the depletion layer of a pn junction. Also it appears to be important that cooling performance should be uniform on the wafer to avoid the growth of hot spots and thermal-runaway itself. © 2002 Wiley Periodicals, Inc. Heat Trans Asian Res, 31(6): 438,455, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/htj.10044 [source] Synthesis and Incorporation of C(5,) -Ethynylated Uracil-Derived Phosphoramidites into RNAHELVETICA CHIMICA ACTA, Issue 12 2004Simon Eppacher The D - allo- and L - talo -hept-6-ynofuranosyluracil-derived phosphoramidites 11A and 11T were prepared in 9,10% yield over eight steps from the previously described propargylic alcohols 1A and 1T, respectively. The corresponding nucleotides were incorporated into rU14 by standard solid-phase synthesis. While the duplex consisting of rU14 with one L - talo -hept-6-ynofuranosyluracil in the middle of the strand and rA14 (I,V) had the same melting point as the reference duplex rU14,rA14 (I,II), the duplex with one D - allo -hept-6-ynofuranosyluracil in the middle of rU14 and rA14 (I,III) melted 1.5° lower than the reference duplex. The duplex I,VI consisting of rU14 with six L - talo -hept-6-ynofuranosyluracils distributed over the entire strand and rA14 showed a melting point that is 11° lower than the reference duplex. The corresponding duplex I,IV of rU14 possessing six D - allo -hept-6-ynofuranosyluracils and rA14 showed a melting point which is more than 20° below the one of the reference duplex. These results are in qualitative agreement with the predictions based on the conformational analysis of the nucleosides and the interference of the ethynyl moiety with the hydration of the oligonucleotides. [source] Evidence for seasonal subglacial outburst events at a polythermal glacier, Finsterwalderbreen, SvalbardHYDROLOGICAL PROCESSES, Issue 12 2001J. L. Wadham Bulk runoff and meteorological data suggest the occurrence of two meltwater outburst events at Finsterwalderbreen, Svalbard, during the 1995 and 1999 melt seasons. Increased bulk meltwater concentrations of Cl, during the outbursts indicate the release of snowmelt from storage. Bulk meltwater hydrochemical data and suspended sediment concentrations suggest that this snowmelt accessed a chemical weathering environment characterized by high rock:water ratios and long rock,water contact times. This is consistent with a subglacial origin. The trigger for both the 1995 and 1999 outbursts is believed to be high rates of surface meltwater production and the oversupply of meltwater to areas of the glacier bed that were at the pressure melting point, but which were unconnected to the main subglacial drainage network. An increase in subglacial water pressure to above the overburden pressure lead to the forcing of a hydrological connection between the expanding subglacial reservoir and the ice-marginal channelized system. The purging of ice blocks from the glacier during the outbursts may indicate the breach of an ice dam during connection. Although subglacial meltwater issued continually from the glacier terminus via a subglacial upwelling during both melt seasons, field observations showed outburst meltwaters were released solely via an ice-marginal channel. It is possible that outburst events are a seasonal phenomenon at this glacier and reflect the periodic drainage of meltwaters from the same subglacial reservoir from year to year. However, the location of this reservoir is uncertain. A 100 m high bedrock ridge traverses the glacier 6·5 km from its terminus. The overdeepened area up-glacier from this is the most probable site for subglacial meltwater accumulation. Copyright © 2001 John Wiley & Sons, Ltd. [source] N-Palmitoyl-4-Hydroxy- L -Proline Palmityl Ester: A Pseudoceramide that Provides Efficient Skin Barrier Repair and ProtectionINTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 1 2006G. Vielhaber Ceramides are the main constituents of the epidermal permeability barrier, and it has been demonstrated that the application of ceramide enriched creams promotes epidermal barrier repair. However, nature-identical ceramides are extremely expensive and difficult to formulate. We therefore developed a new pseudoceramide, N-palmitoyl-4-hydroxy- l -proline palmityl ester (BIO391). Due to its low melting point of £60°C the pseudoceramide BIO391 can easily be incorporated into cosmetic formulations. In addition, it is very safe for use in cosmetics. The efficacy of the pseudoceramide BIO391 was investigated in vivo in a model for detergent-induced barrier disruption. Trans-epidermal water loss, redness, and skin hydration were recorded before and after barrier disruption as well as during the subsequent 9-day treatment with the test products. Barrier repair of skin treated with the pseudoceramide BIO391 was accomplished earlier than that of untreated and vehicle treated skin. Optimum barrier repair was achieved with 1.0% pseudoceramide BIO391 and optimum erythema reduction with 0.5% pseudoceramide BIO391. The optimum dosage could be reduced to 0.1% pseudo-ceramide by synergistic combination with 0.1% (-)-a-bisabolol. In addition, the pseudoceramide BIO391 proved to be as effective as nature-identical ceramides 2 and 3. In summary, N-palmitoyl-4-hydroxy- l -proline palmityl ester is a highly efficient barrier repair agent with efficacy equivalent to that of nature-identical ceramides, and it has excellent formulation properties. [source] Production of zero trans Iranian vanaspati using chemical transesterification and blending techniques from palm olein, rapeseed and sunflower oilsINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 3 2008Jamshid Farmani Summary Chemical transesterification and blending techniques were used for producing zero trans fats suitable for use as Iranian vanaspati. Triple blends of palm olein (POo), rapeseed (RSO) and sunflower oil (SFO) were subjected to two different treatments: (i) blending and then transesterification (BT) and (ii) transesterification of pure POo before blending with RSO and SFO (TB). The changes in slip melting point (SMP), solid fat content (SFC), carbon number (CN) triacylglycerol (TAG) composition, induction period (IP) of oxidation at 120 °C and IP of crystallisation at 20 °C of blends before and after treatments were investigated. Both BT and TB methods resulted in an increase in the CN48 TAG molecules, SMP and SFC, and a decrease in the IP of oxidation and crystallisation of initial blends. Samples made by TB method had higher CN48 TAG content, SMP, SFC and IP of oxidation, and lower IP of crystallisation than those made by BT method. Correlation between SFC at 20 °C and saturated fatty acid (SFA) content of the treated blends indicated that the SFA must be higher than 33.1% and 26.8% for BT and TB methods, respectively, to obtain fats suitable for use as vanaspati. [source] Synthesis, characterization, and degradation of poly(ester-anhydride) for particulate deliveryISRAEL JOURNAL OF CHEMISTRY, Issue 4 2005Sweta Modi A series of poly(ester-anhydride) from poly(lactic acid) and poly(sebacic acid) have been synthesized and characterized. Poly(lactic acid) of molecular weight 2,550 Da has been synthesized from pharmaceutical grade lactic acid. The copolymers are in the molecular weight range of 3,000-15,000 Da, with the higher molecular weights obtained for the polymers with higher sebacic acid content. With increase in sebacic acid content, the melting point is also found to increase. The polymers with 50% or more poly(sebacic acid) content melt between 80 and 84 °C. These polymers have been formulated into microspheres and their degradation studied. Due to their biodegradability and the flexibility to alter their degradation profile, they find a wide application in drug delivery. [source] Polylactide copolymers: Effect of copolymer ratio and end capping on their propertiesADVANCES IN POLYMER TECHNOLOGY, Issue 2 2005D. M. Bigg Abstract Racemic copolymers of polylactic acid were investigated to determine the effect of copolymer ratio on melting point, degree of crystallinity, mechanical properties, and processing behavior. The copolymer ratio was found to have a strong influence on the crystallization behavior of the polymer. In addition to the ratio of the L -form to a random mixture of the D and L forms of the lactic acid in the copolymer, the effect of the polymer's molecular weight was examined. The copolymers were produced from the lactide form of the monomer to achieve weight average molecular weights above 100,000. The molecular weight had a profound influence on processability and rate of crystallization. Other notable factors influencing the properties and processing of the copolymers were the concentration of residual monomer in the polymer, the processing time-temperature history, and the extent of molecular weight degradation during processing. An important factor in the commercial development of biodegradable polymers is the ability to control the rate of degradation. Ideally, the polymer should not degrade during functional use, but degrade quite rapidly when discarded. This paper discusses various aspects associated with the control of the rate of degradation of polylactide copolymers; both from the perspective of stabilizing the polymer during processing and product use, and subsequently accelerating the rate of degradation after disposal. Of particular interest are the influences of molecular weight, crystallinity, end capping, and plasticization. © 2005 Wiley Periodicals, Inc. Adv Polym Techn 24:69,82, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20032 [source] Morphological study of Czochralski-grown lanthanide orthovanadate single crystals and implications on the mechanism of bulk spiral formationJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2 2010Hengjiang Cong Single crystals of monoclinic Nd:LaVO4 with dimensions up to Ø28 × 21,mm have been grown from the near-stoichiometric melt by the Czochralski method, making use of various seed orientations that are perpendicular to the (010), (10), (001) and (00) crystal planes. A sample was also prepared with the seed orientation in an arbitrary direction relative to the crystal. The anisotropic properties of the crystal are manifested in the growth morphology of the as-grown crystals, where different degrees of bulk spiral growth were observed. It was also found that employing the (001) or (00) seed faces severely suppressed the bulk spiral growth, and thus high quality and large-scale Nd:LaVO4 crystals were obtained. The constituent segregation coefficients and high-temperature stability, including the melting point, were determined and evaluated. Based on the attachment energy model of Hartman,Perdok theory, morphology predictions were made for monoclinic LaVO4 and tetragonal YVO4 orthovanadate single crystals. Correlating with the as-grown morphology of both crystals developed along different seed orientations, a theoretical explanation is provided for the influences of seed crystals on bulk spiral formation, crystal quality and utilization ratio. It suggests that breaking the axial symmetry of the ideal atomic level interface between crystal and melt plays a crucial triggering role in bulk spiral formation in the Czochralski growth of lanthanide orthovanadate single crystals. Selecting a proper seed orientation that yields such a highly axially symmetric surface structure consisting of a series of large-area facets with similar growth velocities can greatly reduce bulk spiral formation and thus is preferable in the Czochralski growth of large-sized low-symmetry oxide crystals. [source] Preparation and properties of heat-shrinkable cross-linked low-density polyethyleneADVANCES IN POLYMER TECHNOLOGY, Issue 2 2003J. Morshedian Abstract In this work, heat-shrinkable characteristics of a polyethylene compound were obtained by blending mixtures of low-density polyethylene with varying amount of peroxide. These were then extruded and molded to the required shape and then cross-linked by chemical means, followed by heating and stretching and then cooled to "freeze-in" the oriented polymer structure (elastic memory). A decrease in the melting point and heat of fusion (,Hf), as determined from the DSC melting enthalpies, was observed with an increase in the dicumyl peroxide (DCP) concentration. Tests on the heat shrinkablity of the samples showed that the stretching temperature has a large effect on the shrinkage temperature. The results showed that by increasing the peroxide content, the shrinkage temperature was decreased. The elongation at break decreased with an increase in the DCP concentration. Increasing the temperature in lightly cross-linked samples (low percent DCP) resulted in a reduction in the elongation at break. Increasing the cross-linking density (DCP content) gave an opposite effect. © 2003 Wiley Periodicals, Inc. Adv Polym Techn 22: 112,119, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.10041 [source] Studies on , to , phase transformations in mechanically deformed PVDF filmsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010Vijayakumar R. P. Abstract PVDF cast films were drawn at different temperatures to different draw ratios at constant draw rate to understand the mechanism of , to , phase transformation during mechanical deformation. WAXD and FTIR studies were carried out to determine the formation and content of , phase in the drawn films. Lower stretch temperatures gave higher fractions of , phase. The cast PVDF films were also drawn at suitable temperatures below the PVDF ambient melting point to the draw ratio of 6.4. The highest fraction of , phase obtained in these ultra drawn films was 0.98. SALS studies carried out for films at different stretch ratios show the change in spherulitic structure with the stretching parameters and give information for the understanding of phase transformation during stretching of PVDF films. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Dimethylsilylbis(1-indenyl) zirconium dichloride/methylaluminoxane catalyst supported on nanosized silica for propylene polymerizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Kuo-Tseng Li Abstract A dimethylsilylene-bridged metallocene complex, (CH3)2Si(Ind)2ZrCl2, was supported on a nanosized silica particle, whose surface area was mostly external. The resulting catalyst was used to catalyze the polymerization of propylene to polypropylene. Under identical reaction conditions, a nanosized catalyst exhibited much better polymerization activity than a microsized catalyst. At the optimum polymerization temperature of 55°C, the former had 80% higher activity than the latter. In addition, the nanosized catalyst produced a polymer with a greater molecular weight, a narrower molecular weight distribution, and a higher melting point in comparison with the microsized catalyst. The nanosized catalyst's superiority was ascribed to the higher monomer concentration at its external active sites (which were free from internal diffusion resistance) and was also attributed to its much larger surface area. Electron microscopy results showed that the nanosized catalyst produced polymer particles of similar sizes and shapes, indicating that each nanosized catalyst particle had uniform polymerization activity. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Modeling of coat-hanger die under vibrational extrusionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008Jin-Ping Qu Abstract The distributions of the pulsatile pressure field, the pulsatile velocity field, and the pulsatile resident time of the polymeric melt in the coat-hanger die are derived by using the pulsation of volumetric flow rate and pressure. Subsequently, formulae of the manifold radius and the slope of the manifold are deduced via volumetric flow rate pulsation. Polypropylene (PP) was employed for the experiments of the vibrational extrusion. The results indicate that the average extrusion pressure declines with frequency or amplitude decreasing; the distribution of residence time along the width of the coat-hanger die performs uniformly during the vibrational extrusion process; the theoretical extrusion pressure well agrees with the experimental pressure; the experiments of tensile test, impact test implicate that vibration improves the mechanical properties of products; differential scanning calorimetry testing demonstrates that the melting point of PP is moved to a higher temperature value, and the endothermic enthalpy and the crystallinity are improved as well when superimposing the vibrational force field. Accordingly, the model of the coat-hanger die under vibrational extrusion is well consistent with the experiments. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Biodegradable poly(vinyl alcohol)- graft - poly(,-caprolactone) comb-like polyester: Microwave synthesis and its characterizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Zhaoju Yu Abstract Poly(vinyl alcohol)-initiated microwave-assisted ring opening polymerization of ,-caprolactone in bulk was investigated, and a series of poly(vinyl alcohol)- graft -poly(,-caprolactone) (PVA- g -PCL) copolymers were prepared, with the degree of polymerization (DP) of PCL side chains and the degree of substitution (DS) of PVA by PCL being in the range of 3,24 and 0.35,0.89, respectively. The resultant comb-like PVA- g -PCL copolymers were confirmed by means of FTIR, 1H NMR, and viscometry measurement. The introduction of hydrophilic backbone resulted in the decrease in both melting point and crystallization property of the PVA- g -PCL copolymers comparing with linear PCL. With higher microwave power, the DP of PCL side chains and DS of PVA backbone were higher, and the polymerization reaction proceeded more rapidly. Both the DP and monomer conversion increased with irradiation time, while the DS increased first and then remained constant. With initiator in low concentration, the DP and DS were higher, while the monomer was converted more slowly. Microwaves dramatically improved the polymerization reaction in comparison of conventional heating method. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104, 3973,3979, 2007 [source] Microcellular foaming of PE/PP blendsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Ping Zhang Abstract Three different polyethylene/polypropylene (PE/PP) blends were microcellular foamed and their crystallinities and melt strengths were investigated. The relationship between crystallinity, melt strength, and cellular structure was studied. Experimental results showed that the three blends had similar variation patterns in respect of crystallinity, melt strength, and cellular structure, and these variation patterns were correlative for each blend. For all blends, the melt strength and PP melting point initially heightened and then lowered, the PP crystallinity first decreased, and then increased as the PE content increased. At PE content of 30%, the melt strength and PP melting point were highest and the PP crystallinity was least. The blend with lower PP crystallinity and higher melt strength had better cellular structure and broader microcellular foaming temperature range. So, three blends had best cellular structure at PE content of 30%. Furthermore, when compared with PE/homopolymer (hPP) blend, the PE/copolymer PP (cPP) blend had higher melt strength, better cellular structure, and wider microcellular foaming temperature range, so it was more suited to be microcellular foamed. Whereas LDPE/cPP blend had the broadest microcellular foaming temperature range because of its highest melt strength within three blends. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 4149,4159, 2007 [source] | |||||||||||||||||||||||||||||||||||||||||||