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Sökning: swepub > Högskolan Dalarna > Olsson Mikael > Refereegranskat

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51.
  • Berglund, T., et al. (författare)
  • High velocity compaction of high speed steel powder : possibilities and constraints
  • 2007
  • Ingår i: Proceedings of the Euro Powder Metallurgy Congress and Exhibition, Euro PM 2007. ; , s. 21-26
  • Konferensbidrag (refereegranskat)abstract
    • It is known that gas atomized powders as well as high alloyed metal powders are difficult to press into green bodies using conventional quasi static pressing techniques. However, the development of the high velocity compaction (HVC) technique has expanded the possibility to compact a larger spectrum of metal powders. Although the HVC technique has many similarities with conventional pressing techniques, the high energy impact makes it an interesting technique not only for the pressing of conventional metal powders to green bodies of high density but also for the pressing of "difficult to press metal powders". Today, high speed steel (HSS) is increasingly being used in different types of components. Consequently, there is an increasing interest in the near net shape manufacturing of HSS components. The aim of the present study is to evaluate the possibility to utilize HVC to press green bodies from different types of HSS powder covering both gas and water atomized HSS powders. The results show that the HSS powders investigated differ with respect to compaction properties, i.e. compressibility and green body quality. While the water atomized powders exhibit very good compaction properties, resulting in green bodies of high density, good surface finish and high strength, the gas atomized powders cannot be pressed in the as-atomized condition using HVC. However, agglomerated as well as milled gas atomized HSS powders show significant improved compaction properties compared to the as-atomized powders, although all showed defects of varying sizes depending on the applied energy during compaction.
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52.
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53.
  • Bexell, Ulf, et al. (författare)
  • Characterisation of a Non-Organofunctional Silane Film Deposited on Al, Zn and Al-43.4Zn-1.6Si Alloy-Coated Steel, Part I. Surface Characterization by ToF-SIMS
  • 2001
  • Ingår i: Surface and Interface Analysis. - 0142-2421 .- 1096-9918. ; 31:3, s. 212-222
  • Tidskriftsartikel (refereegranskat)abstract
    • The need to develop new environmentally friendly pretreatments in the surface engineering of metal substrates has become more and more important.This is mainly due to the toxic and carcinogenic properties of the chromium-based surface pretreatments frequently used in the industry. During the last decade, simple solution-dip silane-based pretreatments have emerged as promising candidates for the replacement of currently used pretreatments of metals. Recent investigations have shown that the performance of these newly developed pretreatments is strongly dependent on the chemical composition and structure of the silane film and consequently a lot of work, based on advanced surface analytical techniques, is needed in order to characterize these properties. In the present study, time-of-flight secondary ion mass spectrometry (ToF-SIMS) has been used to characterize the structure of thin films of the non-organofunctional silane 1,2-bis(triethoxysilyl)ethane (BTSE) deposited on three different metal substrates, i.e. Al, Zn and Al-43.4Zn-1.6Si (AlZn) alloy-coated steel. Of special interest was an evaluation of the influence of substrate material on the structure and composition of the silane films. The results show that the BTSE silane forms a thin, evenly distributed film over the substrate surfaces and that the molecular structure of the silane film is independent of the type of metal substrate. Analysis of the molecular ions in the positive mode shows that the surface structure of the BTSE silane is very complex and that the BTSE condensates via one to three SiOSi bridges. Also, the results show that the BTSE silane is not fully hydrolysed using a hydrolysing time of 1 h. Finally, if an alcohol is used as a solvent for the BTSE there is a clear chemical interaction between the alcohol and the silane, resulting in an exchange of alkoxy groups between the alcohol and the silane. Copyright © 2001 John Wiley & Sons, Ltd.
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54.
  • Bexell, Ulf, et al. (författare)
  • Characterisation of a Non-Organofunctional Silane Film Deposited on Al, Zn and Al-43.4Zn-1.6Si Alloy Coated Steel, Part II. Interfacial Characterization by ToF-SIMS and AES
  • 2001
  • Ingår i: Surface and Interface Analysis. - 0142-2421 .- 1096-9918. ; 31:3, s. 223-231
  • Tidskriftsartikel (refereegranskat)abstract
    • Time-of-flight secondary ion mass spectrometry (ToF-SIMS) has been used to analyse the interface between a non-organofunctional silane and three different metal substrates (aluminium, zinc and an aluminium-zinc alloy). Ion etching using Ga+ ions was used to expose the interfacial region. Ion fragments from the samples were examined carefully where supposed metal-oxygen-silicon ion fragments should appear in the mass spectra. From high mass resolution spectra it was concluded that there exists an AlOSi+ ion fragment at nominal mass m/z = 71 amu on the aluminium and aluminium-zinc alloy substrates and a ZnOSi+ ion fragment at nominal mass m/z = 108 amu on the zinc and aluminium-zinc alloy substrates. These results are further enhanced by the fact that the characteristic ion pattern of ZnOSi+-type ion fragments, composed of different naturally stable zinc and silicon isotopes, in the mass range m/z = 108-112 amu showed the expected relative peak height relations. The presence of these metal-oxygen-silicon ion fragments is a strong indication that chemical interaction between the silane and the metal substrates exists and that the nature of this interaction is due to the formation of a covalent bond between the silane and the metal substrate. Copyright © 2001 John Wiley & Sons, Ltd.
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55.
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56.
  • Bexell, Ulf, et al. (författare)
  • High temperature oxidation of plastically deformed ferritic interconnect steel
  • 2011
  • Ingår i: ECS Transactions. - Pennington : The Electrochemical Society. - 1938-5862 .- 1938-6737. ; 35:1, s. 2463-2470
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, thin sheets of a 22% Cr ferritic steel, Sandvik Sanergy HT has been coated with a thin metallic cobalt film. Samples of the coated steel sheet were exposed to two different forming experiments simulating different aspects of sheet metal forming and post high temperature oxidation. The results show that the metallic cobalt film cracks when the steel sheet is subjected to biaxial straining but that the cracks heal at high temperature. Material subjected to modified scratch testing i.e. simulating the contact between sheet metal and forming tool will oxidize in the same manner as non-scratched material. Also, from high temperature corrosion point of view there is no difference between materials formed under lubricated or dry conditions when oxidized. However, from a tribological point of view a lubricated contact situation is preferred.
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57.
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58.
  • Bexell, Ulf, et al. (författare)
  • Tribological Characterisation of an Organic Coating by the use of ToF-SIMS
  • 2003
  • Ingår i: Applied Surface Science. - 0169-4332 .- 1873-5584. ; 203-204, s. 596-599
  • Tidskriftsartikel (refereegranskat)abstract
    • ToF-SIMS has been used to analyse tribological induced chemical changes of organic coatings deposited on steel strip hot-dip coated with a 55.0% Al–43.4% Zn–1.6% Si alloy (Aluzink). The organic coating was a styrene–acrylic co-polymer containing different forming additives. The forming properties of the organic coatings were evaluated with modified scratch testing. The friction curves show that organic coated hot-dip coated steel displays significantly better tribological properties, i.e. lower coefficient of friction and lower wear, as compared to hot-dip coated steel. Furthermore, the organic coatings showing the highest material transfer tendency also show the highest wear. ToF-SIMS spectra show that a transfer film consisting of species from the organic coating is formed on the ball counter surface. Finally, a combination of SEM and ToF-SIMS analysis shows that mechanical failure of the coating dominates, i.e. no tribochemical changes of the coatings could be detected in the wear track.
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59.
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60.
  • Canovic, Sead, et al. (författare)
  • Microstructural investigation of the initial oxidation of the FeCrAlRE alloy Kanthal AF in dry and wet O2 at 600 and 800°C
  • 2010
  • Ingår i: Journal of the Electrochemical Society. - : The electrochemical society. - 0013-4651 .- 1945-7111. ; 157:6, s. C223-C230
  • Tidskriftsartikel (refereegranskat)abstract
    • The FeCrAlRE (where RE is reactive element) alloy Kanthal AF was exposed isothermally at 600 and 800°C for 72 h in dry O2 and in O2 with 10 vol % H2O. The mass gains were 3–5 times higher at the higher temperature. The presence of water vapor increased the oxidation rate at 800°C, while no significant effect was observed at 600°C. A thin two-layered oxide formed at 600°C: an outer (Fe,Cr)2O3 corundum-type oxide, containing some Al, and an inner, probably amorphous, Al-rich oxide. At 800°C a two-layered oxide formed in both environments. The inner layer consisted of inward grown a-Al2O3. In dry O2 the originally formed outward grown g-Al2O3 had transformed to a-Al2O3 after 72 h. Water vapor stabilized the outward grown g-Al2O3 and hence no transformation occurred after 72 h in humid environment. RE-rich oxide particles with varying composition (Y, Zr, and Ti) were distributed in the base oxide at both temperatures and in both environments. The RE-rich particles were separated from the alloy substrate by a layer of Al-rich oxide. At 800°C the Y-rich RE particles were surrounded by thick oxide patches in both dry and humid O2.
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