Change search
Refine search result
1 - 9 of 9
CiteExportLink to result list
Permanent link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Rows per page
  • 5
  • 10
  • 20
  • 50
  • 100
  • 250
Sort
  • Standard (Relevance)
  • Author A-Ö
  • Author Ö-A
  • Title A-Ö
  • Title Ö-A
  • Publication type A-Ö
  • Publication type Ö-A
  • Issued (Oldest first)
  • Issued (Newest first)
  • Created (Oldest first)
  • Created (Newest first)
  • Last updated (Oldest first)
  • Last updated (Newest first)
  • Disputation date (earliest first)
  • Disputation date (latest first)
  • Standard (Relevance)
  • Author A-Ö
  • Author Ö-A
  • Title A-Ö
  • Title Ö-A
  • Publication type A-Ö
  • Publication type Ö-A
  • Issued (Oldest first)
  • Issued (Newest first)
  • Created (Oldest first)
  • Created (Newest first)
  • Last updated (Oldest first)
  • Last updated (Newest first)
  • Disputation date (earliest first)
  • Disputation date (latest first)
Select
The maximal number of hits you can export is 250. When you want to export more records please use the Create feeds function.
  • 1.
    Boubitsas, Dimitrios
    RISE, SP – Sveriges Tekniska Forskningsinstitut, CBI Betonginstitutet AB, Betong & Berg. Lund University, Sweden.
    Chloride transport and chloride threshold values: studies on concretes and mortars with Portland cement and limestone blended cement2016Doctoral thesis, comprehensive summary (Other academic)
    Abstract [en]

    Reinforced concrete is one of the most widely used building materials and if it is properly designed and produced, it is an extremely durable material with a service life up to 100 years. However, under certain environmental conditions the service life of reinforced concrete structures is more limited. Deterioration ofconcrete structure is in most cases caused by the penetration of aggressive media from the surrounding environment. Chloride initiated reinforcement corrosion is one of the major causes of deterioration of Concrete structures. One conflicting issue is how replacing Portland cement with mineral additions influences chlorideinitiated reinforcement corrosion. This issue is of immediate interest, as there is a steady growth in the use of cement blended with mineral additions, such as blast-furnace slag, fly ash and limestone filler. This is done by the cement and concrete industry to reduce the CO2 emissions linked to Portland cement manufacturing, bylimiting the use of clinker in the cement.The main objective of this work has been to further clarify the role of limestone filler as partial substitute to Portland cement on the two main decisive parameters for chloride induced reinforcement corrosion: chloride ingress rate and chloride threshold values. In the first part of this work the chloride ingress was studied both with accelerated laboratory methods and also after field exposure. The initial focus for the second part of the study was to determine the chloride threshold values for the binders investigated in the first part, so a comprehensive view of the effect of limestone addition on chloride initiated corrosion could be presented.However, during the work the need for the development of a practice-related method for determining the chloride threshold values was identified and the focus of the research was redirected to meet that need.The efficiency of limestone filler concerning chloride ingress showed to be dependent on replacement ratio, time (age) and on the test method. It was not possible to draw any rigid conclusion of the limestone filler’s efficiency regarding chloride ingress. But part of the inconsistency in the results was identified to be that limestone filler has two opposite effects on chloride ingress, on one hand contribute to a refinement of microstructure and on the other hand diminishing the chloride binding.The steel surface condition was shown to have a strong effect on the corrosion initiation, and can likely be one of the most decisive parameters attributing to the variability in the reported chloride threshold values obtained in laboratory experiments. The chloride threshold value for the sulphate resistant Portland cement fromthe laboratory experiments was estimated to be about 1% by weight of binder. For the concrete with limestone blended cement (CEM II/A-LL 42.5R) tested in this work the chloride threshold value was at the same level as for the sulphate resistant Portland cement. From the field study but with a somewhat different definition ofchloride threshold value, a chloride threshold value of about 1% by weight of binder was also estimated for ordinary Portland cement and sulphate resistance Portland with 5% silica fume exposed to marine environment.

  • 2.
    Ejenstam, Lina
    et al.
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Polymer och fiber. KTH Royal Institute of Technology, School of Chemical Science and Engineering, Department of Chemistry, Division of Surface and Corrosion Science.
    Swerin, Agne
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik. KTH Royal Institute of Technology, School of Chemical Science and Engineering, Department of Chemistry, Division of Surface and Corrosion Science.
    Pan, J.
    Claesson, Per M.
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik. Department of Chemistry Surface and Corrosion Science, KTH Royal Institute of Technology.
    Corrosion protection by hydrophobic silica particle-polydimethylsiloxane composite coatings2015In: Corrosion Science, ISSN 0010-938X, E-ISSN 1879-0496, Vol. 99, p. 89-97Article in journal (Refereed)
    Abstract [en]

    In this study, the time-dependent corrosion protection ability of 10-15. μm thin polydimethylsiloxane-nanoparticle composite coatings was evaluated using mainly open circuit potential and electrochemical impedance spectroscopy measurements. The best result was obtained for the coating containing 20. wt% hydrophobic silica nanoparticles, where it was possible to achieve protection for almost 80 days in 3. wt% NaCl solution. The protective properties offered by this coating are suggested to be due to a synergistic effect of the hydrophobicity of the polydimethylsiloxane matrix and the prolonged diffusion path caused by addition of hydrophobic silica particles.

  • 3.
    Ejenstam, Lina
    et al.
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Polymer och fiber. KTH Royal Institute of Technology, School of Chemical Science and Engineering, Department of Chemistry, Division of Surface and Corrosion Science.
    Tuominen, Mikko
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik.
    Haapanen, J.
    Mäkelä, J. M.
    Pan, J.
    Swerin, Agne
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik. KTH Royal Institute of Technology, Division of Surface and Corrosion Science.
    Claesson, Per M.
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik. Department of Chemistry Surface and Corrosion Science, KTH Royal Institute of Technology.
    Long-term corrosion protection by a thin nano-composite coating2015In: Applied Surface Science, ISSN 0169-4332, E-ISSN 1873-5584, Vol. 357, no Part B, p. 2333-2342Article in journal (Refereed)
    Abstract [en]

    We report and discuss the corrosion protective properties of a thin nano-composite coating system consisting of an 11μm thick polyester acrylate (PEA) basecoat, covered by an approximately 1-2μm thick layer of TiO2 nanoparticles carrying a 0.05μm thick hexamethyl disiloxane (HMDSO) top coat. The corrosion protective properties were evaluated on carbon steel substrates immersed in 3wt% NaCl solution by open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) measurements. The protective properties of each layer, and of each pair of layers, were also evaluated to gain further understanding of the long-term protective properties offered by the nano-composite coating. The full coating system showed excellent corrosion protective properties in the corrosive environment of 3wt% NaCl-solution for an extended period of 100 days, during which the coating impedance, at the lower frequency limit (0.01Hz), remained above 108 Ωcm2. We suggest that the excellent corrosion protective properties of the complete coating system is due to a combination of (i) good adhesion and stability of the PEA basecoat, (ii) the surface roughness and the elongated diffusion path provided by the addition of TiO2 nanoparticles, and (iii) the low surface energy provided by the HMDSO top coat.

  • 4.
    Fast, Lars
    et al.
    RISE - Research Institutes of Sweden.
    Lang, Jenny
    RISE - Research Institutes of Sweden.
    Nygren, Kristian
    Impact Coatings AB.
    Bodén, Andreas
    Power Cell AB.
    Ofstad, A.B.
    Leisner, Peter
    RISE - Research Institutes of Sweden. Jönköping University.
    Successful Development of Coating for BipolarPlates for Proton exchange Membrane Fuel Cell2015Conference paper (Refereed)
  • 5. Hedberg, Y. S.
    et al.
    Pradhan, S.
    Cappellini, F.
    Karlsson, M. -E
    Blomberg, Eva
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Life Science. KTH Royal Institute of Technology, Sweden.
    Karlsson, H. L.
    Odnevall Wallinder, I.
    Hedberg, J. F.
    Electrochemical surface oxide characteristics of metal nanoparticles (Mn, Cu and Al) and the relation to toxicity2016In: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 212, p. 360-371Article in journal (Refereed)
    Abstract [en]

    Most metal nanoparticles (NPs), except noble metal NPs, rapidly form a thin surface oxide in ambient conditions. The protective properties of these oxides improve or worsen depending on the environment, e.g., the human lung. Several properties, including the chemical/electrochemical stability and defect density, determine the capacity of these surface oxides to hinder the bulk metal from further oxidation (corrosion). The aim of this study was to investigate whether electrochemical surface oxide characterization of non-functionalized base metal NPs of different characteristics (Al, Mn and Cu) can assist in understanding their bioaccessibility (metal release) in cell media (DMEM+) and their cytotoxic properties following exposure in lung epithelial (A549) cells. The composition and valence states of surface oxides of metal NPs and their electrochemical activity were investigated using an electrochemical technique based on a graphite paste electrode to perform cyclic voltammetry in buffer solutions and open circuit potential measurements in DMEM+. The electrochemical surface oxide characterization was complemented and verified by Raman spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The open circuit potential trends in DMEM+ correlated well with metal release results in the same solution, and provided information on the kinetics of oxide dissolution in the case of Cu NPs. Extensive particle agglomeration in cell medium (DMEM+) was observed by means of photon-cross correlation spectroscopy for all metal NPs, with sedimentation taking place very quickly. As a consequence, measurements of the real dose of added non-functionalized metal NPs to cell cultures for cytotoxicity testing from a sonicated stock solution were shown necessary. The cytotoxic response was found to be strongly correlated to changes in physico-chemical and electrochemical properties of the surface oxides of the metal NPs, the most potent being Cu NPs, followed by Mn NPs. No cytotoxicity was observed for Al NPs. The electrochemical surface oxide characterization corresponded well with other tools commonly used for nanotoxicological characterization and provided additional information.

  • 6. Jafarzadeh, S.
    et al.
    Claesson, Per M.
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik. Department of Chemistry Surface and Corrosion Science, KTH Royal Institute of Technology.
    Sundell, P. -E
    Tyrode, E.
    Pan, J.
    Active corrosion protection by conductive composites of polyaniline in a UV-cured polyester acrylate coating2016In: Progress in organic coatings, ISSN 0300-9440, E-ISSN 1873-331X, Vol. 90, p. 154-162Article in journal (Refereed)
    Abstract [en]

    Polyaniline doped with phosphoric acid (PANI-PA) was synthesized and characterized by impedance and Raman spectroscopy. Exposure to UV-light resulted in a slight decrease in the PANI's electrical conductivity and no significant change in the oxidation state (of an emeraldine salt). Composite coatings containing 0, 1, 3 and 5 wt.% PANI-PA in a UV-curable polyester acrylate (PEA) resin were prepared and applied on polished carbon steel. Closely packed PANI-PA particles of several tens of nanometers were observed inside the composite coating by scanning electron microscopy, and a connected conductive network across the film was detected by Peak Force TUNA atomic force microscopy. The evolution of open circuit potential and impedance data during long-term exposure to 3 wt.% NaCl electrolyte revealed that the short-term barrier-type corrosion protection provided by the insulating PEA coating can be turned into a long-term and active protection by addition of as little as 1 wt.% PANI-PA to the formulation. Stable ennoblement in the corrosive media was observed for the coatings containing conducting polymer up to 3 wt.%. However, higher content of PANI-PA (5 wt.%) led to poorer protective properties, probably due to the hydrophilicity of PANI-PA facilitating water transport in the coating and the presence of potentially weaker spots in the film. An iron oxide layer was found to fully cover the metal surface beneath the coatings containing PANI-PA after final failure observed by electrochemical testing.

  • 7. Li, J.
    et al.
    Ecco, L.
    Ahniyaz, Anwar
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik.
    Fedel, Michele
    RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor, Material och ytteknik.
    Pan, J.
    In situ AFM and electrochemical study of a waterborne acrylic composite coating with CeO2 nanoparticles for corrosion protection of carbon steel2015In: Journal of the Electrochemical Society, ISSN 0013-4651, E-ISSN 1945-7111, Vol. 162, no 10, p. C610-C618Article in journal (Refereed)
    Abstract [en]

    The corrosion protection of a waterborne acrylic composite coating with 1 wt% ceria nanoparticles (CeNP) coated on carbon steel in 3 wt% NaCl solution was investigated by ex-situ and in situ as well as electrochemical atomic force microscopy (AFM) observations, combined with open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) measurements. The synthesized CeNP were stabilized by acetic acid. The transmission electron microscopy characterization showed fine nano-size of as-synthesized CeNP, the ex-situ AFM imaging revealed uniform dispersion of the CeNP in the composite coating and greatly reduced nano-sized pinholes in the coating. The in situ and electrochemical (EC) AFM investigations indicate release of some CeNP and aggregates from the coating surface and then precipitation of some particles and cerium-compounds during the exposure. The OCP and EIS results demonstrated that the addition of 1 wt% CeNP leads to a significantly improved long term barrier type corrosion protection of the waterborne acrylic composite coating for carbon steel in 3 wt% NaCl solution. The beneficial effect of the CeNP is attributed to the blocking of nano-sized defects and inhibition by the cerium compounds originated from the acetic acid stabilized CeNP.

  • 8.
    Zhu, Baiwei
    et al.
    Jönköping University, Sweden.
    Fedel, Michele
    University of Trento, Italy.
    Andersson, Nils-Eric
    Jönköping University, Sweden.
    Leisner, Peter
    RISE - Research Institutes of Sweden, Safety and Transport, Electronics. Jönköping University, Sweden.
    Deflorian, Flavio
    University of Trento, Italy.
    Zanella, Caterina
    Jönköping University, Sweden.
    Effect of Si content and morphology on corrosionresistance of anodized cast Al-Si alloys2017In: Journal of the Electrochemical Society, ISSN 0013-4651, E-ISSN 1945-7111, Vol. 164, no 7, p. C435-C441Article in journal (Refereed)
    Abstract [en]

    This paper investigates the influence of Si content and Si particle morphology on the corrosion protection of anodized oxide layers on Al-Si alloys. Two Al alloys with low Si concentrations (2.43 wt-% and 5.45 wt-%, respectively) were studied and compared with 6082-T6 via electrochemical impedance spectroscopy (EIS) in 3 wt-% NaCl solution prior to oxide layer sealing. Si particles were also modified by the addition of Sr to study the influence of Si particle morphology on the corrosion protection of the oxide layer. The EIS showed that the corrosion protection provided by the oxide layer on Al-Si alloys is significantly affected by the presence of Si particles. Si particles make the oxide layer locally thinner and more defective in the eutectic region, thereby increasing the ease of substrate corrosion attack. However, the addition of Sr can improve the corrosion protection of anodized Al-Si alloys significantly. Furthermore, it was proved that higher Si level influences negatively the anodized oxide corrosion protection due to the higher amount of cracks and defects, but Sr modification is efficient in preventing this negative effect.

  • 9.
    Zhu, Baiwei
    et al.
    Jönköping University, Sweden.
    Fedel, Michele
    University of Trento, Italy.
    Andersson, Nils-Eric
    Jönköping University, Sweden.
    Leisner, Peter
    RISE - Research Institutes of Sweden, Safety and Transport, Electronics. Jönköping University, Sweden.
    Deflorian, Flavio
    University of Trento, Italy.
    Zanella, Caterina
    Jönköping University, Sweden.
    Influence of the Srmodification and post-treatment on corrosion resistance of oxide layer of cast Al-(low)Si alloys2017Conference paper (Refereed)
1 - 9 of 9
CiteExportLink to result list
Permanent link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
v. 2.35.5