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EN
A multiscale model for simulating the hydrodynamic behavior of catalytic bale packings has been proposed. This model combines computational fluid dynamics (CFD) and macroscopic calculation. At small scale calculation, the CFD model includes 3-D volume-of-fluid (VOF) simulation within representative elementary unit (REU) under unsteady-state conditions. The REU constitutes gauze and catalyst domain, and porous media model is applied. At large scale calculation, a new mechanistic model deduced from the unit network model is employed. Based on liquid split proportion from small scale calculation, liquid distribution of the entire bale packing can be predicted. To evaluate different packing design, three common bale arrangements, i.e. one-bale, nine-bales and seven-bales, are compared. The area-weighted Christiansen uniformity coefficient is introduced to assess the distribution performance. A comparison between simulation and experimental results is made to validate the multiscale model. The present methodology is proved to be effective to analysis and design of catalytic distillation columns.
EN
The general trend in soft matter is to study systems of increasing complexity covering a wide range in time and frequency. Mechanical spectroscopy is a powerful tool for understanding the structure and relaxation dynamics of these materials over a large temperature range and frequency scale. In this work, we collect a few recent applications using low-frequency mechanical spectroscopy for elucidating the structural changes and relaxation dynamics in soft matter, largely based on the author’s group. We illustrate the potential of mechanical spectroscopy with three kinds of soft materials: colloids, polymers and granular systems. Examples include structural changes in colloids, segmental relaxations in amorphous polymers, and resonant dissipation of grain chains in three-dimensional media. The present work shows that mechanical spectroscopy has been applied as a necessary and complementary tool to study the dynamics of such complex systems.
PL
Ogólnym trendem w miękkiej materii jest, aby badać układy o rosnącej złożoności, obejmującej szeroki zakres czasu i częstotliwości. Spektroskopia mechaniczna jest potężnym narzędziem dla zrozumienia struktury i dynamiki relaksacji tych materiałów w szerokim zakresie temperatury i skali częstotliwości. W niniejszej pracy, zebraliśmy kilka ostatnich zastosowań spektroskopii mechanicznej niskiej częstotliwości do poznania zmian strukturalnych i dynamiki relaksacji w miękkiej materii, w dużej mierze opartych na grupie autorów. Opisujemy potencjał spektroskopii mechanicznej w przypadku trzech rodzajów materiałów miękkich: koloidów, polimerów i układów ziarnistych. Przykłady obejmują zmiany strukturalne w koloidach, segmentowe relaksacje amorficznych polimerów, i rezonansowe rozpraszanie łańcuchów ziaren w mediach trójwymiarowych. Niniejsza praca pokazuje, że spektroskopię mechaniczną zastosowano jako niezbędne i uzupełniające narzędzie do badania dynamiki takich systemów złożonych.
EN
The ESR dating method requires to describe the evolution of the ESR signal intensities vs. increasing gamma doses, then to extrapolate the equivalent dose of radiation received by the sample since its deposition using mathematical fitting. The function classically used to describe the growth curves of ESR aluminium signal in quartz was recently discussed and challenged for Lower Pleisto-cene sediments. In the present work, some alluvial sediments sampled in Upper Pleistocene fluvial terraces of the Yellow River system (China) permit us to test the application of another extrapolation function (linear + exponential) recently proposed for Lower Pleistocene sediments. The equivalent doses obtained here for the recent deposits of the Yellow River system and the corresponding ages are promising and indicate the potential of ESR to date quartz deposits from Upper Pleistocene times.
EN
A novel method of immobilizing horse radish peroxidase enzyme (HRP) onto the surface of gold nanoparticles (GNPs) was developed. As a result, a high-activity bionanoconjugates was obtained through utilizing the biotin-streptavidin (SA) system. The HRP-SA-GNP bionanoconjugate with high activity was conveniently prepared through the biotin- avidin system. Compared with the HRP-GNP bioconjugate prepared through the traditional electrostatic absorption method, the enzyme activity per GNPs of this new bionanoconjugate was enhanced by 10 times. Moreover, the enzyme activity of this bionanoconjugate was controllable. The above method of bionanoconjugation preparation has promising applications In the fi elds including preparing highly active bio-nanoprobe and immobilized enzyme.
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