TY - JOUR A1 - Bäßler, Ralph A1 - Bettge, Dirk A1 - Bender, R. A1 - Féron, D. A1 - Mills, D. A1 - Ritter, S. A1 - de Graeve, I. A1 - Dugstad, A. A1 - Grassini, S. A1 - Hack, T. A1 - Halama, M. A1 - Han, E.-H. A1 - Harder, T. A1 - Hinds, G. A1 - Kittel, J. A1 - Krieg, R. A1 - Leygraf, C. A1 - Martinelli, L. A1 - Mol, A. A1 - Neff, D. A1 - Nilsson, J.-O. A1 - Odnevall, I. A1 - Paterson, S. A1 - Paul, S. A1 - Prosek, T. A1 - Raupach, M. A1 - Revilla, R. I. A1 - Ropital, F. A1 - Schweigart, H. A1 - Szala, E. A1 - Therryn, H. A1 - Tidblad, J. A1 - Virtanen, S. A1 - Volovitch, P. A1 - Watkinson, D. A1 - Wilms, M. A1 - Winning, G. A1 - Zheludkevich, M. T1 - La corrosion: un défi pour une société durable N2 - Une transition mondiale vers des systèmes énergétiques plus durables, abordables et fiables a été initiée par l’accord de Paris et l’Agenda 2030 des Nations unies pour un développement durable. Il s’agit là d’un défi industriel majeur car les systèmes et infrastructures énergétiques résilients au changement climatique exigent de se positionner pour le long terme. Se pencher sur le comportement dans la durée des matériaux structurels - principalement des métaux et des alliages - s’impose alors comme une nécessité. Dans cette optique, « La corrosion : un défi pour une société durable »présente une série de cas montrant l’importance de la tenue à la corrosion et de la protection anticorrosion des métaux et des alliages pour le développement de systèmes durables, économiques et fiables de production d’énergie. KW - Corrosion KW - Coûts de la corrosion KW - Protection KW - Anticorrosion KW - Stratégies deprévention PY - 2023 DO - https://doi.org/10.51257/a-v1-cor2000 SN - 2555-5383 VL - 2023 IS - Avril SP - 1 EP - 23 CY - Saint-Denis, France AN - OPUS4-57927 LA - fra AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bäßler, Ralph A1 - Mietz, Jürgen A1 - Raupach, M. A1 - Goltermann, P. T1 - Use of Embeddable Sensors in an Integrated Monitoring System for Reinforced Concrete Structures T2 - Corrosion 2003 CY - San Diego, CA, USA DA - 2003-03-16 KW - Chloride Induced Corrosion KW - Integrated Monitoring System KW - Embedded Sensors PY - 2003 IS - 03436 SP - 1(?) EP - 13(?) PB - NACE International CY - Houston, Tex. AN - OPUS4-2381 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Angst, U.M. A1 - Geiker, M.R. A1 - Alonso, M.C. A1 - Polder, R. A1 - Isgor, O.B. A1 - Elsener, B. A1 - Wong, H. A1 - Michel, A. A1 - Hornbostel, K. A1 - Gehlen, C. A1 - François, R. A1 - Sanchez, M. A1 - Criado, M. A1 - Sørensen, H. A1 - Hansson, C. A1 - Pillai, R. A1 - Mundra, Shishir A1 - Gulikers, J. A1 - Raupach, M. A1 - Pacheco, J. A1 - Sagüés, A. T1 - The effect of the steel-concrete interface on chloride-induced corrosion initiation in concrete: a critical review by RILEM TC 262-SCI N2 - The steel–concrete interface (SCI) is known to influence corrosion of steel in concrete. However, due to the numerous factors affecting the SCI—including steel properties, concrete properties, execution, and exposure conditions—it remains unclear which factors have the most dominant impact on the susceptibility of reinforced concrete to corrosion. In this literature review, prepared by members of RILEM technical committee 262-SCI, an attempt is made to elucidate the effect of numerous SCI characteristics on chloride-induced corrosion initiation of steel in concrete. We use a method to quantify and normalize the effect of individual SCI characteristics based on different literature results, which allows comparing them in a comprehensive context. It is found that the different SCI characteristics have received highly unbalanced research attention. Parameters such as w/b ratio and cement type have been studied most extensively. Interestingly, however, literature consistently indicates that those parameters have merely a moderate effect on the corrosion susceptibility of steel in concrete. Considerably more pronounced effects were identified for (1) steel properties, including metallurgy, presence of mill scale or rust layers, and surface roughness, and (2) the moisture state. Unfortunately, however, these aspects have received comparatively little research attention. Due to their apparently strong influence, future corrosion studies as well as developments towards predicting corrosion initiation in concrete would benefit from considering those aspects. Particularly the working mechanisms related to the moisture conditions in microscopic and macroscopic voids at the SCI is complex and presents major opportunities for further research in corrosion of steel in concrete. KW - Steel-concrete interface KW - Interfacial transition zone KW - Durability KW - Corrosion KW - Inhomogeneity KW - Variability PY - 2019 DO - https://doi.org/10.1617/s11527-019-1387-0 VL - 52 IS - 4 SP - 88-1 EP - 88-25 PB - Springer Nature AN - OPUS4-48689 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Nikoonasab, Ali A1 - Müller, Thoralf A1 - Licht, M. A1 - Raupach, M. A1 - Gluth, Gregor ED - Rogge, Andreas ED - Meng, Birgit T1 - Sulfides in the pore solutions of GGBFS-containing concretes - Influence on the corrosion of reinforcing steel N2 - Steel corrosion in sulfide-containing solutions is a challenge in various environments, such as reinforced concrete structures. In concrete, sulfides are introduced by ground granulated blast-furnace slag (GGBFS), used in standard cements and alkali-activated materials (AAMs), affecting steel corrosion. This study examined steel in synthetic GGBFS-containing cement pore solutions using electrochemical techniques. Compared to Portland cement solutions, steel in sulfide-containing solutions exhibits lower open circuit potentials and polarisation resistances. Thus, Portland cement concrete corrosion assessment standards are unsuitable for GGBFScontaining concrete. T2 - 11. Jahrestagung des DAfStb mit 63. Forschungskolloquium der BAM Green Intelligent Building CY - Berlin, Germany DA - 16.10.2024 KW - Corrosion KW - Reinforcing steel PY - 2024 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-612963 SN - 978-3-9818564-7-7 SP - 55 EP - 59 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-61296 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Nikoonasab, Ali A1 - Licht, M. A1 - Weiler, L. A1 - Achenbach, R. A1 - Raupach, M. A1 - Gluth, Gregor T1 - Pore Solution composition of GGBFS-containing cement pastes N2 - Ground Granulated Blast-Furnace Slag (GGBFS), a by-product of the iron-making process, has gained significant attention as a supplementary cementitious material and has become increasingly popular in recent years due to its remarkable properties. GGBFS can significantly reduce the environmental impact of cement production when it comes to building concrete structures. GGBFS can either be blended with ordinary Portland cement (OPC) (up to a 90% replacement), or it can be used in the production of alkali-activated materials (AAMs). However, a comprehensive understanding of the pore solution composition is necessary for understanding various aspects of cementitious materials and their durability, including corrosion behavior, passivation of steel, and resistance to deteriorative processes. In the present work, the pore solutions of seven different GGBFS-containing cements (alkali-activated slag, alkali-activated slag/fly ash blends, a hybrid alkaline cement, CEM III/C, and CEM III/B) were extracted and analysed by inductively coupled plasma-optical emission spectroscopy, ion chromatography, pH, redox potential, and conductivity measurements. For comparison, a Portland cement pore solution was analysed similarly. The Concentrations of reduced sulfur were noteworthy in all GGBFS-containing cements, particularly in alkali-activated cements, where concentrations were notably higher compared to standard cements. The redox potentials of the pore solutions were primarily dictated by the concentrations of reduced sulfur, although other factors may contribute. Additionally, sulfur species in the pore solutions had an impact on pH, electrical conductivity, and other properties pertinent to the corrosion of reinforcements. T2 - RILEM Spring Convention 2024 & Conference on Advanced Construction Materials and Processes for a Carbon Neutral Society CY - Milan, Italy DA - 10.04.2024 KW - GGBFS KW - AAM KW - Sulfide KW - Pore solution composition KW - Redox potential PY - 2024 AN - OPUS4-59960 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mundra, Shishir A1 - Samson, G. A1 - Masi, G. A1 - Achenbach, R. A1 - Bastidas, D. M. A1 - Bernal, S. A. A1 - Bignozzi, M. C. A1 - Criado, M. A1 - Cyr, M. A1 - Gartner, N. A1 - von Greve-Dierfeld, S. A1 - Legat, A. A1 - Nikoonasab, Ali A1 - Provis, J. L. A1 - Raupach, M. A1 - Gluth, Gregor T1 - Stahlkorrosion in alkalisch aktivierten Bindemitteln und Betonen: Anwendung elektrochemischer Methoden N2 - Alkalisch aktivierte Bindemittel (AAB) und Betone können herkömmliche Zemente beziehungsweise Betone potentiell in vielen Anwendungen ersetzen und dadurch den CO2-Fußabdruck der Bauindustrie wesentlich verkleinern. Zur Untersuchung der Stahlkorrosion in bewehrten („armierten“) Betonbauteilen werden elektrochemische Methoden wie Messungen des Freien Korrosionspotentials, des Polarisationswiderstands oder von Stromdichte-Potential-Kurven eingesetzt. Diese Methoden und die etablierten Grenzwerte zur Detektion von Korrosion sind für die Anwendung bei herkömmlichen Zementen beziehungsweise Betonen entwickelt und erprobt worden. Neue Forschungsergebnisse demonstrieren, dass Unterschiede zwischen den Porenlösungszusammensetzungen von herkömmlichen Zementen und bestimmten AAB sowie anderen schlackehaltigen Zementen erhebliche Unterschiede bei den Ergebnissen der elektrochemischen Messungen bewirken und damit zur fehlerhaften Detektion von Stahlkorrosion führen können. Ursache hierfür sind vor allem reduzierte Schwefelspezies in den Porenlösungen von AAB und anderen schlackehaltigen Zementen. KW - Zement KW - Hüttensandmehl KW - Schlacke KW - Sulfid KW - Korrosion PY - 2023 UR - https://bit.ly/GIT-Gluth UR - https://analyticalscience.wiley.com/content/magazine-do/git-labor-fachzeitschrift-10-2023 SN - 0016-3538 VL - 67 IS - 10 SP - 28 EP - 31 PB - Wiley-VCH AN - OPUS4-58573 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Licht, M. A1 - Nikoonasab, Ali A1 - Gluth, Gregor A1 - Raupach, M. ED - Claßen, M. ED - Hegger, J. ED - Matschei, T. ED - Raupach, M. T1 - Alkali-aktivierte Hüttensandbetone – CO2-reduzierte Bindemittel mit hohem Korrosionsschutzpotential N2 - Durch den Ersatz von Portlandzement können alkali-aktivierte Bindemittel einen bedeutenden Beitrag zur Verringerung der durch die Zementklinkerherstellung verursachten CO2-Emissionen leisten. Für die Verwendung von alkali-aktivierten Bindemitteln in Stahlbetonkonstruktionen, die Chloriden oder Carbonatisierung ausgesetzt sind, ist die Fähigkeit des Stahls, den passiven Zustand zu erreichen und aufrechtzuerhalten, von großer Bedeutung. Die Prozesse der Deckschichtbildung von Stahl in alkali-aktivierten Materialien unterscheiden sich jedoch zum Teil grundlegend von denen in Portlandzementen. Alkali-aktivierte Hüttensandbetone weisen gute technische Eigenschaften auf, bisher fehlen jedoch grundlegende Kenntnisse bzgl. ihrer schützenden Wirkung bei korrosiven Angriffen. Dies ist vor allem auf ihre sulfidhaltige Porenlösung zurückzuführen, welche die elektrochemischen Eigenschaften der Stahloberfläche beeinflusst und die Verwendung herkömmlicher Bewertungsmaßstäbe erschwert. Es werden erste Ergebnisse eines DFG-Forschungsprojektes vorgestellt, in dem das Passivierungsverhalten von Stahl in alkali-aktivierten Hüttensandmörteln unterschiedlicher Zusammensetzungen sowie in Mörteln auf Basis hüttensandhaltiger Normzemente untersucht wird. Über einen Zeitraum von mindestens 28 Tagen werden an Zylinderprüfkörpern im 3-Elektroden-Aufbau das Ruhepotential sowie die Polarisationswiderstände der Stahlelektroden ermittelt. T2 - 10. DAfStb-Jahrestagung mit 62. Forschungskolloquium CY - Aachen, Germany DA - 26.09.2023 KW - Bewehrung KW - Stahlkorrosion KW - Hüttensandmehl KW - Sulfid PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-593775 DO - https://doi.org/10.18154/RWTH-2023-06676 SP - 233 EP - 238 PB - RWTH Aachen CY - Aachen AN - OPUS4-59377 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nikoonasab, Ali A1 - Licht, M. A1 - Weiler, L. A1 - Achenbach, R. A1 - Raupach, M. A1 - Gluth, Gregor T1 - Pore solution compositions and redox potentials of ground granulated blast furnace slag-containing cement pastes N2 - The pore solutions of hardened ground granulated blast furnace slag (GGBFS)-containing cements differ from the pore solutions of other cements with effects on reinforcement corrosion, application of electrochemical methods and immobilisation of radioactive waste. In the present study, the pore solutions of seven different GGBFS-containing cements (alkali-activated slag, alkali-activated slag/fly ash blends, hybrid alkaline cement (HAC), CEM III/C and CEM III/B) were extracted and their elemental and sulfate concentration, pH, redox potential and conductivity were determined; a Portland cement (CEM I) pore solution was analysed analogously. The silicon and aluminium concentrations of the alkali-activated cements increased with fly ash fraction, reaching values up to 5 mM and 10 mM, respectively, and thus were considerably higher than those of the standard cements. The redox potentials of the pore solutions of the GGBFS-containing cements were in the range from −100 mV to –500 mV vs Ag/AgCl, that is considerably lower than that of the Portland cement (8–20 mV vs Ag/AgCl), with the value depending on the GGBFS fraction and whether the cements were alkali-activated or not. These results indicate that the effects of reduced sulfur species from GGBFS in cements are more pronounced in alkali-activated materials, including HAC, and increase with GGBFS fraction. KW - Alkali-activated materials KW - Ground granulated blast furnace slag KW - Sulfide KW - Redox potential KW - Pore solution PY - 2025 DO - https://doi.org/10.1680/jadcr.25.00041 SN - 1751-7605 SN - 0951-7197 SP - 1 EP - 12 PB - Emerald AN - OPUS4-64619 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mundra, S. A1 - Samson, G. A1 - Masi, G. A1 - Achenbach, R. A1 - Bastidas, D. M. A1 - Bernal, S. A. A1 - Bignozzi, M. C. A1 - Criado, M. A1 - Cyr, M. A1 - Gartner, N. A1 - von Greve-Dierfeld, S. A1 - Legat, A. A1 - Nikoonasab, Ali A1 - Provis, J. L. A1 - Raupach, M. A1 - Gluth, Gregor T1 - Application of electrochemical methods for studying steel corrosion in alkali-activated materials N2 - Alkali-activated materials (AAMs) are binders that can complement and partially substitute the current use of conventional cement. However, the present knowledge about how AAMs protect steel reinforcement in concrete elements is incomplete, and uncertainties exist regarding the application of electrochemical methods to investigate this issue. The present review by EFC WP11-Task Force ‘Corrosion of steel in alkali-activated materials’ demonstrates that important differences exist between AAMs and Portland cement, and between different classes of AAMs, which are mainly caused by differing pore solution compositions, and which affect the outcomes of electrochemical measurements. The high sulfide concentrations in blast furnace slag-based AAMs lead to distinct anodic polarisation curves, unusually low open circuit potentials, and low polarisation resistances, which might be incorrectly interpreted as indicating active corrosion of steel reinforcement. No systematic study of the influence of the steel–concrete interface on the susceptibility of steel to corrosion in AAMs is available. Less common electrochemical methods present an opportunity for future progress in the field. KW - Alkali-activated materials KW - Reinforcement corrosion KW - Steel corrrosion KW - Electrochemical methods KW - Concrete PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-572241 DO - https://doi.org/10.1002/maco.202313743 SN - 1521-4176 VL - 74 IS - 7 SP - 988 EP - 1008 PB - Wiley-VCH CY - Weinheim AN - OPUS4-57224 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -