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71.
72.
During a recent design study involving a critically stressed “tongue-and-groove” type compression joint of dissimilar materials, a novel technique was conceived for nullifying the effects of an otherwise high local stress-concentration factor. In principle, the nominal stresses in the tongue-and-groove portions of the joint are forced to be uniform. For idealizedfit conditions, the stress concentration in the fillet under this stress-equalized condition is theorized to approach unity (1.00). In the present paper, experimental verification is provided. 相似文献
73.
Here, we present a fast and simple hydrogen peroxide assay that is based on time-resolved fluorescence. The emission intensity of a complex consisting of terbium ions (Tb3+) and phthalic acid (PA) in HEPES buffer is quenched in the presence of H2O2 and this quenching is concentration-dependent. The novel PATb assay detects hydrogen peroxide at a pH range from 7.5 to 8.5 and with a detection limit of 150 nmol L−1 at pH 8.5. The total assay time is less than 1 min. The linear range of the assay can be adapted by a pH adjustment of the aqueous buffer and covers a concentration range from 310 nmol L−1 to 2.56 mmol L−1 in total which encompasses four orders of magnitude. The assay is compatible with high concentrations of all 47 tested inorganic and organic compounds. The PATb assay was applied to quantify H2O2 in polluted river water samples. In conclusion, this fast and easy-to-use assay detects H2O2 with high sensitivity and precision. 相似文献
74.
To describe material behaviour more precisely than nowadays, tomorrows simulation software will include multi-scale homogenisation techniques. State of the art are various scale bridging strategies, like FE-ODE, FE-Phasefield or FE2-Method. We are dealing with the FE2-Method, see [3], [4], which gives us the possibility to take the geometric, discrete micro-structure of a material into account. Furthermore, it allows to integrate enhanced continuum mechanical models. Here, we are researching on two-scale approach with poro-mechanical coupling based on the Theory of Porous Media (TPM), for more details see [1] or [2]. The framework is demanding and need a lot of computational effort. In order to receive industrial recognition, it is necessary to decrease the computation runtime. One way to go is definitely using high performance cluster. (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
75.
Klodian Xhanari Kristin Syverud Gary Chinga-Carrasco Kristofer Paso Per Stenius 《Cellulose (London, England)》2011,18(2):257-270
Adsorption isotherms of single and double chain cationic surfactants with different chain length (cetyltrimethyl-, didodecyl-
and dihexadecyl ammonium bromide) onto cellulose nanofibrils were determined. Nanofibrillated cellulose, also known as microfibrillated
cellulose (MFC), with varying contents of carboxyl groups (different surface charge) was prepared by TEMPO-mediated oxidation
followed by mechanical fibrillation. The fibril charge was characterized by potentiometric and conductometric titration. Surfactant
adsorption was verified by Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Photoelectron Spectroscopy (XPS). Wetting
and adhesion of water onto fibril films was determined by contact angle measurements. Small aggregates (admicelles) of surfactant
were shown to form on the nanofibril surfaces, well below critical micelle concentrations. The results demonstrate the possibility
of using cationic surfactants to systematically control the degree of water wettability of cellulose nanofibrils. 相似文献
76.
A valveless microdevice has been developed for the integration of solid phase extraction (SPE) and polymerase chain reaction (PCR) on a single chip for the short tandem repeat (STR) analysis of DNA from a biological sample. The device consists of two domains--a SPE domain filled with silica beads as a solid phase and a PCR domain with an ~500 nL reaction chamber. DNA from buccal swabs was purified and amplified using the integrated device and a full STR profile (16 loci) resulted. The 16 loci Identifiler? multiplex amplification was performed using a non-contact infrared (IR)-mediated PCR system built in-house, after syringe-driven SPE, providing an ~80-fold and 2.2-fold reduction in sample and reagent volumes consumed, respectively, as well as an ~5-fold reduction in the overall analysis time in comparison to conventional analysis. Results indicate that the SPE-PCR system can be used for many applications requiring genetic analysis, and the future addition of microchip electrophoresis (ME) to the system would allow for the complete processing of biological samples for forensic STR analysis on a single microdevice. 相似文献
77.
Shavorskiy A Aksoy F Grass ME Liu Z Bluhm H Held G 《Journal of the American Chemical Society》2011,133(17):6659-6667
The coadsorption of water with organic molecules under near-ambient pressure and temperature conditions opens up new reaction pathways on model catalyst surfaces that are not accessible in conventional ultrahigh-vacuum surface-science experiments. The surface chemistry of glycine and alanine at the water-exposed Cu{110} interface was studied in situ using ambient-pressure photoemission and X-ray absorption spectroscopy techniques. At water pressures above 10(-5) Torr a significant pressure-dependent decrease in the temperature for dissociative desorption was observed for both amino acids, accompanied by the appearance of a new CN intermediate, which is not observed for lower pressures. The most likely reaction mechanisms involve dehydrogenation induced by O and/or OH surface species resulting from the dissociative adsorption of water. The linear relationship between the inverse decomposition temperature and the logarithm of water pressure enables determination of the activation energy for the surface reaction, between 213 and 232 kJ/mol, and a prediction of the decomposition temperature at the solid-liquid interface by extrapolating toward the equilibrium vapor pressure. Such experiments near the equilibrium vapor pressure provide important information about elementary surface processes at the solid-liquid interface, which can be retrieved neither under ultrahigh vacuum conditions nor from interfaces immersed in a solution. 相似文献
78.
Xhanari K Syverud K Chinga-Carrasco G Paso K Stenius P 《Journal of colloid and interface science》2011,356(1):58-62
The nature of layers formed by cellulose nanofibrils that had been surface modified (hydrophobized) at the oil/water (o/w) interface was investigated. The aim of the study was to clarify the mechanism underlying the excellent ability of these nanoparticles to stabilize emulsions. Layers of hydrophobized nanofibrillated cellulose spread at the o/w interface were deposited on glass slides by the Langmuir-Blodgett deposition technique. Overall evaluation of layer structures was performed by image analysis based on a Quadtree decomposition of images obtained from a flatbed scanner. A more detailed characterization of the layer structures was performed by Atomic Force Microscopy (AFM), and Field-Emission Scanning Electron Microscopy (FE-SEM). The results show that nanofibrils that were able to stabilize emulsions occur as single, dispersed fibrils or form large, network-like aggregates at the o/w interface. Fibrils that were insufficiently hydrophobized and therefore did not stabilize emulsions were only partially deposited and formed small, compact aggregates. We conclude that it is likely that the network formation is the main mechanism by which the fibrils prevent coalescence of emulsion droplets. 相似文献
79.
Mysak ER Smith JD Ashby PD Newberg JT Wilson KR Bluhm H 《Physical chemistry chemical physics : PCCP》2011,13(16):7554-7564
X-ray photoelectron spectroscopy (XPS) is used to monitor the heterogeneous reaction of hydroxyl radicals (OH) and ozone with thin films (~5 ?) of coronene. Detailed elemental and functional group analysis of the XPS spectra reveals that there is a competition between the addition of oxygenated functional groups (functionalization) and the loss of material (volatilization) to the gas phase. Measurements of the film thickness and elemental composition indicate that carbon loss is as important as the formation of new oxygenated functional groups in controlling how the oxygen-to-carbon ratio (O/C) of the coronene film evolves during the surface reaction. When the O/C ratio of the film is small (~0.1) the addition of functional groups dominates changes in film thickness, while for more oxygenated films (O/C > 0.3) carbon loss is an increasingly important reaction pathway. Decomposition of the film occurs via the loss of both carbon and oxygen atoms when the O/C ratio of the film exceeds 0.5. These results imply that chemically reduced hydrocarbons, such as primary organic aerosol, age in the atmosphere by forming new oxygenated functional groups, in contrast to oxygenated secondary organic aerosol, which decompose by a heterogeneous loss of carbon and/or oxygen. 相似文献
80.
We show that the value function of a singular stochastic
control problem is equal to the integral of the value function
of an associated optimal stopping problem. The connection is
proved for a general class of diffusions using the
method of viscosity solutions. 相似文献