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Träfflista för sökning "WFRF:(Geiger T.) srt2:(2010-2014)"

Sökning: WFRF:(Geiger T.) > (2010-2014)

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1.
  • Hollertz, Rebecca, et al. (författare)
  • Improvement of toughness and electrical properties of epoxy composites with carbon nanotubes prepared by industrially relevant processes
  • 2011
  • Ingår i: Nanotechnology. - : IOP Publishing. - 0957-4484 .- 1361-6528. ; 22:12, s. 125702-
  • Tidskriftsartikel (refereegranskat)abstract
    • The addition of carbon nanotubes (CNTs) to polymeric matrices or master batches has thepotential to provide composites with novel properties. However, composites with a uniformdispersion of CNTs have proved to be difficult to manufacture, especially at an industrial scale.This paper reports on processing methods that overcome problems related to the control andreproducibility of dispersions. By using a high pressure homogenizer and a three-rollcalendaring mill in combination, CNT reinforced epoxies were fabricated by mould castingwith a well dispersed nanofiller content from 0.1 to 2 wt%. The influence of the nano-carbonreinforcements on toughness and electrical properties of the CNT/epoxies was studied. Asubstantial increase of all mechanical properties already appeared at the lowest CNT content of0.1 wt%, but further raising the nanofiller concentration only led to moderate further changes.The most significant enhancement was obtained for fracture toughness, reaching up to 82%.The low percolation thresholds were confirmed by electrical conductivity measurements on thesame composites yielding a threshold value of only about 0.01 wt%. As corroborated by athorough microscopic analysis of the composites, mechanical and electrical enhancement pointsto the formation of an interconnected network of agglomerated CNTs.
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2.
  • Geiger, T., et al. (författare)
  • Initial quantitative proteomic map of 28 mouse tissues using the SILAC mouse
  • 2013
  • Ingår i: Molecular & Cellular Proteomics. - 1535-9476 .- 1535-9484. ; 12:6, s. 1709-1722
  • Tidskriftsartikel (refereegranskat)abstract
    • Identifying the building blocks of mammalian tissues is a precondition for understanding their function. In particular, global and quantitative analysis of the proteome of mammalian tissues would point to tissue-specific mechanisms and place the function of each protein in a whole-organism perspective. We performed proteomic analyses of 28 mouse tissues using high-resolution mass spectrometry and used a mix of mouse tissues labeled via stable isotope labeling with amino acids in cell culture as a "spike-in" internal standard for accurate protein quantification across these tissues. We identified a total of 7,349 proteins and quantified 6,974 of them. Bioinformatic data analysis showed that physiologically related tissues clustered together and that highly expressed proteins represented the characteristic tissue functions. Tissue specialization was reflected prominently in the proteomic profiles and is apparent already in their hundred most abundant proteins. The proportion of strictly tissue-specific proteins appeared to be small. However, even proteins with household functions, such as those in ribosomes and spliceosomes, can have dramatic expression differences among tissues. We describe a computational framework with which to correlate proteome profiles with physiological functions of the tissue. Our data will be useful to the broad scientific community as an initial atlas of protein expression of a mammalian species.
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