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Träfflista för sökning "WFRF:(Münger Peter) srt2:(2000-2004)"

Sökning: WFRF:(Münger Peter) > (2000-2004)

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1.
  • Carlberg, M H, et al. (författare)
  • Dynamics of self-interstitial structures in body-centred-cubic W studied by molecular dynamics simulation
  • 2000
  • Ingår i: Journal of Physics. - 0953-8984 .- 1361-648X. ; 12:1, s. 79-86
  • Tidskriftsartikel (refereegranskat)abstract
    • This study concerns a molecular dynamics (MD) simulation, using the embedded-atom method (EAM), of the self-diffusion of an interstitial in the bcc metal tungsten (W) at 2000 K. It is found that the interstitial moves only along (111) diagonals and that the switches to other nonparallel directions take place through a two-dimensional process. The (011) dumb-bell is central to this process. Movement along the (111) diagonals takes place through (111) crowdions occupying 2-6 lattice sites. The probabilities of a direction switch and a move are 0.249 and 0.751, respectively. Translating the complicated movement mechanism into the simple picture of interstitial hopping between lattice points, the diffusion velocity is calculated to be 520 m s(-1), and the activation energy for the interstitial self-diffusion is calculated to be 0.54 eV/interstitial.
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2.
  • Chirita, Valeriu, et al. (författare)
  • Cluster diffusion and surface morphological transitions on Pt (111) via reptation and concerted motion
  • 2000
  • Ingår i: Thin Solid Films. - 0040-6090 .- 1879-2731. ; 370:1, s. 179-185
  • Tidskriftsartikel (refereegranskat)abstract
    • Embedded-atom molecular dynamics simulations were used to follow the diffusion dynamics of compact Pt clusters with up to 19 atoms on Pt (111) surfaces. The results reveal a novel cluster diffusion mechanism, involving successive shear translations of adjacent subcluster regions, which give rise to reptation, a snake-like gliding motion. We show that for compact clusters with 4 to 6 atoms, this mechanism competes energetically with that of island diffusion through concerted motion. However, as the cluster size increases from > 7 to ? 20 atoms, reptation becomes the energetically favored diffusion mechanism. The concerted shear motion of subcluster regions, leading to reptation, is also shown to play a significant role in dendritic-to-compact morphological transitions of Pt island.
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3.
  • Münger, Peter, et al. (författare)
  • Adatom/vacancy interactions and interlayer mass transport in small two-dimensional Pt clusters on Pt(1 1 1)
  • 2003
  • Ingår i: Surface Science. - 0039-6028 .- 1879-2758. ; 539:1-3
  • Tidskriftsartikel (refereegranskat)abstract
    • We use embedded-atom molecular dynamics simulations to follow the dynamics of adatoms, vacancies, and adatom/vacancy pairs on two-dimensional hexagonal Pt19 clusters on Pt(1 1 1) surfaces at 1000 K. All configurations are found to be quite stable and have essentially the same migration mobilities as compact hexagonal clusters. However, the presence of a single vacancy dramatically decreases the lifetime of an adatom on the cluster by a factor of three. This occurs primarily through an enhancement of the rate of push-out/exchange reactions at the outer cluster edge resulting from vacancy-induced softening of edge atom bonds. Overall, adatoms in the presence of vacancies descend to the terrace via vacancy filling 10% of the time, and through reactions with outer cluster edges the remaining 90%. Direct vacancy filling mechanisms are analogous to, and have similar activation energies with, those at outer cluster edges: adatom hopping over descending steps and push-out/exchange reactions. © 2003 Elsevier B.V. All rights reserved.
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4.
  • Suuronen, Erik J., et al. (författare)
  • Functional innervation in tissue engineered models for in vitro study and testing purposes
  • 2004
  • Ingår i: Toxicological Sciences. - : Oxford University Press (OUP). - 1096-6080 .- 1096-0929. ; 82:2, s. 525-533
  • Tidskriftsartikel (refereegranskat)abstract
    • The biotechnology industry is rapidly expanding and the emerging field of tissue engineering is projected to have a high impact in the near future. Recently the field of cellular, drug, and prosthetic delivery has melded with the field of tissue engineering to make simulated tissues. In addition to their roles as tissue substitutes for transplantation, these simulated tissues may provide more accurate models and environments for toxicology testing and the study of peripheral nerves. The current study demonstrates the importance of innervation, in general, for the function of engineered tissues. We observe that the presence of nerves in a tissue engineered (TE) human cornea model enhances the growth of the epithelium and the formation of its protective mucin layer. Innervation also confers protection to the epithelium from chemical insult, as determined by the level of post-treatment epithelial cell death. We demonstrate differential responses of the nerves to chemical stimuli by changes in intracellular sodium as measured by 2-photon microscopy. The 2-photon imaging techniques also allow for the visualization and study of the fine sensory axon fibers within the 3-dimensional tissue. This work demonstrates a role for innervation in the protective quality and function of the engineered tissue, and the potential to use the nerves themselves as indicators of the severity of an insult. These results are important to consider for the development of any optimized TE models for in vitro study and testing purposes.
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5.
  • Suuronen, Erik J., et al. (författare)
  • Innervated human corneal equivalents as in vitro models for nerve-target cell interactions
  • 2003
  • Ingår i: The FASEB Journal. - : Federation of American Society of Experimental Biology (FASEB). - 0892-6638 .- 1530-6860. ; 17, s. 170-
  • Tidskriftsartikel (refereegranskat)abstract
    • A sensory nerve supply is crucial for optimal tissue function. However, the mechanisms for successful innervation and the signaling pathways between nerves and their target tissue are not fully understood. Engineered tissue substitutes can provide controllable environments in which to study tissue innervation. We have therefore engineered human corneal substitutes that promote nerve in-growth in a pattern similar to in vivo re-innervation. We demonstrate that these nerves (a) are morphologically equivalent to natural corneal nerves; (b) make appropriate contact with target cells; (c) can generate action potentials; (d) respond to chemical and physical stimuli; and (e) play an important role in the overall functioning of the bioengineered tissue. This model can be used for studying the more general topics of nerve ingrowth or regeneration and the interaction between nerves and their target cells and, more specifically, the role of nerves in corneal function. This model could also be used as an in vitro alternative to animals for safety and efficacy testing of chemicals and drugs.
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