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991.
This article presents numerical simulations of the laminar flow of lubricating greases in a channel with rectangular cross section. Three greases with different consistencies (NLGI grades 00, 1, and 2) have been considered in three different configurations composed of a rectangular channel without restrictions, one rectangular step restriction, and one double-lip restriction. The driving pressure drop over the channel spans from 30 to 250 kPa. The grease rheology is described by the Herschel-Bulkley rheology model, and both the numerical code and rheology model have been validated with analytical solutions and flow measurements using micro-particle image velocimetry. 相似文献
992.
Christoph Schmerbauch Jesus Gonzalez‐Julian Robert Röder Carsten Ronning Olivier Guillon 《Journal of the American Ceramic Society》2014,97(6):1728-1735
We report the sintering behavior of nanocrystalline zinc oxide under external AC electric field between 0 and 160 V/cm. In situ acquisition of density by means of laser dilatometry, evaluation of specimen temperature, real‐time measurement of electric field and current help analyze this peculiar behavior. Field strength and blocking electrodes significantly affect densification and microstructure, which was evaluated in the vicinity of the flash event and for the fully sintered material. High current densities flow through the sample at high electric fields, entailing a sudden increment of the temperature estimated to several hundreds of K and an exaggerated grain growth. In contrast, low current density flows through the sample at lower electric fields, which guarantees normal grain growth and highest final density. Macroscopic photoluminescence measurements give insights into the development of the defect structure. Electric fields are expected to enhance defect mobility, explaining the high densification rates observed during the sintering process. 相似文献
993.
Jiadong Zang Ming Li Derek C. Sinclair Wook Jo Jürgen Rödel 《Journal of the American Ceramic Society》2014,97(5):1523-1529
The electrical and dielectric properties of (1 ? x)(0.94Bi1/2Na1/2TiO3–0.06BaTiO3)–x(K0.5Na0.5NbO3) with x = 0, 0.03, 0.09, 0.18 have been investigated by impedance spectroscopy over a wide temperature range. The dc conductivity of the ceramics follows the Arrhenius law with an activation energy ranging from ~1.20 to 1.50 eV. Measurements under different atmospheres show the materials exhibit n‐type semiconducting behavior at elevated temperatures. The presence of a highly polarizable phase for all compositions is revealed by electric modulus (M″) spectra. The Burns temperature decreases with increasing KNN content. The change in temperature‐dependent permittivity with composition is explained by the difference in thermal evolution of polar nanoregions induced by the addition of KNN. 相似文献
994.
Maria Teresa Calejo Anna‐Lena Kjøniksen Atoosa Maleki Bo Nyström Sverre Arne Sande 《应用聚合物科学杂志》2014,131(7)
In this work, a hydrophobically modified (HM) chitosan derivative was prepared by covalent linkage of C12 groups to the chitosan backbone. HM‐chitosan microparticles were prepared according to an emulsification‐solvent evaporation method and naltrexone (NTX) was used as a model drug. For comparison, unmodified chitosan and poly lactic‐co‐glycolic acid (PLGA) microparticles were also tested as carriers for NTX. HM‐chitosan formed viscous semi‐dilute solutions, suggesting a high level of chain entanglements and hydrophobic associations. HM‐chitosan microparticles generally showed higher production yield and encapsulation efficiency, as compared with chitosan and PLGA. The burst release shown by chitosan microparticles was significantly reduced when using the HM‐chitosan derivative. An enhanced control of drug release was observed over at least 50 days. PLGA particles demonstrated inferior controlled release properties as compared to HM‐chitosan subsequent to the initial release stage. These results revealed the potential of hydrophobic modification of chitosan as a means to improve the stability and sustained delivery properties of the polymer. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40055. 相似文献
995.
Platinum electrocatalysts were prepared using PtCl4 as a starting material and 1-decylamine, N,N-dimethyldecylamine, 1-dodecylamine, N,N-dimethyldodecylamine, 1-hexadecylamine, and 1-octadecylamine as surfactants. These surfactants were used for the first time in this synthesis to determine whether the primary and/or tertiary structure and/or chain length of the surfactants, affects the size and/or activity of the catalysts in C1–C3 alcohol electro-oxidation reactions. Electrochemical measurements (cyclic voltammetry and chronoamperometry) indicated that the highest electrocatalytic performance was observed for the Pt nanocatalysts that were stabilized by N,N-dimethyldecylamine, and this has a tertiary amine structure with a short chain length (R = C10H21). The high performance may be due to the high electrochemical surface area, Pt(0)/Pt(IV) ratio, %Pt utility, and roughness factor (R f). X-ray photoelectron spectroscopy, X-ray diffraction, atomic force microscopy, and transmission electron microscopy were used to determine the parameters that affect the catalytic activities. 相似文献
996.
Nasir Mahmood Asad Ullah Khan Klaus Werner Stöckelhuber Amit Das Dieter Jehnichen Gert Heinrich 《应用聚合物科学杂志》2014,131(11)
This article reports the preparation and characterization of multiwalled carbon nanotubes (MWCNTs)‐filled thermoplastic polyurethane–urea (TPUU) and carboxylated acrylonitrile butadiene rubber (XNBR) blend nanocomposites. The dispersion of the MWCNTs was carried out using a laboratory two roll mill. Three different loadings, that is, 1, 3, and 5 wt % of the MWCNTs were used. The electron microscopy image analysis proves that the MWCNTs are evenly dispersed along the shear flow direction. Through incorporation of the nanotubes in the blend, the tensile modulus was increased from 9.90 ± 0.5 to 45.30 ± 0.3 MPa, and the tensile strength at break was increased from 25.4 ± 2.5 to 33.0 ± 1.5 MPa. The wide angle X‐ray scattering result showed that the TPUU:XNBR blends were arranged in layered structures. These structures are formed through chemical reactions of ? NH group from urethane and urea with the carboxylic group on XNBR. Furthermore, even at a very low loading, the high degree of nanotubes dispersion results in a significant increase in the electrical percolation threshold. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40341. 相似文献
997.
The tableting process causes a temperature increase due to dissipation of energy. Therefore, with time the temperature of the tablets and the tablet press increases. Depending on the calculated tablet temperature, this temperature increase is discussed for different compression forces and lubricant concentrations. Two different measurement techniques are presented and compared. 相似文献
998.
Designing oligomeric ethylene terephtalate building blocks by chemical recycling of polyethylene terephtalate 下载免费PDF全文
The intelligent recycling of plastics waste is a major concern. Because of the widespread use of polyethylene terephtalate, considerable amounts of PET waste are generated that are ideally re‐introduced into the material cycle by generating second generation products without loss of materials performance. Chemical recycling methods are often expensive and entail environmentally hazardous by‐products. Established mechanical methods generally provide materials of reduced quality, leading to products of lower quality. These drawbacks can be avoided by the development of new recycling methods that provide materials of high quality in every step of the production cycle. In the present work, oligomeric ethylene terephthalate with defined degrees of polymerization and defined molecular weight is produced by melt‐mixing PET with different quantities of adipic acid as an alternative pathway of recycling PET with respect to conventional methods, offering ecofriendly and economical aspects. Additionally, block‐copolyesters of defined block length are designed from the oligomeric products. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39786. 相似文献
999.
Kinetic modeling of hemicellulose hydrolysis in the presence of homogeneous and heterogeneous catalysts 下载免费PDF全文
Tapio Salmi Dmitry Yu. Murzin Päivi Mäki‐Arvela Bright Kusema Bjarne Holmbom Stefan Willför Johan Wärnå 《American Institute of Chemical Engineers》2014,60(3):1066-1077
Kinetic models were developed for the hydrolysis of O‐acetyl‐galactoglucomannan (GGM), a hemicellulose appearing in coniferous trees. Homogeneous and heterogeneous acid catalysts hydrolyze GGM at about 90°C to the monomeric sugars galactose, glucose, and mannose. In the presence of homogeneous catalysts, such as HCl, H2SO4, oxalic acid, and trifluoroacetic acid, the hydrolysis process shows a regular kinetic behavior, while a prominent autocatalytic effect was observed in the presence of heterogeneous cation‐exchange catalysts, Amberlyst 15 and Smopex 101. The kinetic models proposed were based on the reactivities of the nonhydrolyzed sugar units and the increase of the rate constant (for heterogeneous catalysts) as the reaction progresses and the degree of polymerization decreases. General kinetic models were derived and special cases of them were considered in detail, by deriving analytical solutions for product distributions. The kinetic parameters, describing the autocatalytic effect were determined by nonlinear regression analysis. The kinetic model described very well the overall kinetics, as well as the product distribution in the hydrolysis of water soluble GGM by homogeneous and heterogeneous catalysts. The modelling principles developed in the work can be in principle applied to hydrolysis of similar hemicelluloses as well as starch and cellulose. © 2014 American Institute of Chemical Engineers AIChE J, 60: 1066–1077, 2014 相似文献
1000.