1,551 research outputs found
Initiation and stagnation of room temperature grain coarsening in cyclically strained gold films
Despite the large number of experiments demonstrating that grains in a
metallic material can grow at room temperature due to applied mechanical load,
the mechanisms and the driving forces responsible for mechanically induced
grain coarsening are still not understood. Here we present a systematic study
of room temperature grain coarsening induced by cyclic strain in thin
polymer-supported gold films. By means of detailed electron backscatter
diffraction analysis we were able to capture both the growth of individual
grains and the evolution of the whole microstructure on the basis of
statistical data over thousands of grains. The experimental data are reported
for three film thicknesses with slightly different microstructures and three
different amplitudes of cyclic mechanical loading. Although different kinds of
grain size evolution with increasing cycle number are observed depending on
film thickness and strain amplitude, a single model based on a thermodynamic
driving force is shown to be capable to explain initiation and stagnation of
grain coarsening in all cases. The main implication of the model is that the
grains having lower individual yield stress are coarsening preferentially.
Besides, it is demonstrated that the existence of local shear stresses imposed
on a grain boundary is not a necessary requirement for room-temperature grain
coarsening
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Research into defectiveness of welded joints of steam pipes operated over a long time
Проведено аналіз пошкоджуваності металу зварних з'єднань паропроводів із Cr–Mo–V теплостійких перлітних сталей, які тривалий час експлуатуються в умовах повзучості та малоциклової втоми. Наведені зварні з'єднання пошкоджуються одночасно порами повзучості та тріщинами втоми. Розглянуто фактори, які викликають пошкоджуваність, а також залежність пошкоджуваності від структури зварних з'єднань і умов експлуатації. Їх пошкоджуваність переважно має крихкий характер
Metastable phases and "metastable" phase diagrams
The work discusses specifics of phase transitions for metastable states of
substances. The objects of condensed media physics are primarily equilibrium
states of substances with metastable phases viewed as an exception, while the
overwhelming majority of organic substances investigated in chemistry are
metastable. It turns out that at normal pressure many of simple molecular
compounds based on light elements (these include: most hydrocarbons; nitrogen
oxides, hydrates, and carbides; carbon oxide (CO); alcohols, glycerin etc) are
metastable substances too, i.e. they do not match the Gibbs' free energy
minimum for a given chemical composition. At moderate temperatures and
pressures, the phase transitions for given metastable phases throughout the
entire experimentally accessible time range are reversible with the equilibrium
thermodynamics laws obeyed. At sufficiently high pressures (1-10 GPa), most of
molecular phases irreversibly transform to more energy efficient polymerized
phases, both stable and metastable. These transformations are not consistent
with the equality of the Gibbs' free energies between the phases before and
after the transition, i.e. they are not phase transitions in "classical"
meaning. The resulting polymeric phases at normal pressure can exist at
temperatures above the melting one for the initial metastable molecular phase.
Striking examples of such polymers are polyethylene and a polymerized
modification of CO. Many of energy-intermediate polymeric phases can apparently
be synthesized by the "classical" chemistry techniques at normal pressure.Comment: 5 pages, 4 figure
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