TY - CONF A1 - Gluth, Gregor T1 - Activities related to quality infrastructure in the construction industry in Africa T2 - africa re:load 2013 CY - Weimar, Germany DA - 2013-07-11 PY - 2013 N1 - Geburtsname von Priebe, Nsesheye Susan: Msinjili, N. S. - Birth name of Priebe, Nsesheye Susan: Msinjili, N. S. AN - OPUS4-29023 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Shrinkage and bond behaviour of one-part alkali-activated mortars N2 - Mortars for application on concrete, e.g. repair mortars or protective coatings, need to have a durable bond to the substrate. This bond is determined by the adhesion between the two materials and by the differential deformations of the mortar and the substrate. In the present contribution, the hygric deformations (shrinkage/expansion) of novel one-part alkali-activated mortars and their bond to concrete substrates are studied. Shrinkage of the mortars was studied at 50 % r.H., while expansion was studied on mortars stored over an open water surface (> 99% r.H.). The bond behaviour was studied by pull-off tests according to DIN EN 1542 and by optical microscopy. The alkali-activated mortars exhibit hygric deformations much lower than the deformations of an established, commercial mortar for sewer maintenance that was tested as reference in parallel with the alkali-activated mortars. The bond behaviour of the alkali-activated mortars depends strongly on their mix-design and curing. Optical microscopy showed that in the mortars with lower bond strength, cracks developed in the mortar during curing. Mortars with appropriate mix-design and curing did not exhibit cracking, and their pull-off strength (up to > 3 MPa) conformed to the requirements of relevant standards. T2 - International Conference on Sustainable Materials, Systems and Structures (SMSS 2019) CY - Rovinj, Croatia DA - 20.03.2019 KW - Alkali-activated materials KW - Bond strength KW - Hygric deformations KW - Repair mortars KW - Sewer repair PY - 2019 AN - OPUS4-47618 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Investigation of calcined brick clays from Central Germany for use as SCM N2 - The production of Portland cement causes a substantial environmental impact, since the calcination of limestone results in high emissions of carbon dioxide. The use of supplementary cementitious materials such as calcined clays as partial replacement for Portland cement offers a solution to limit this environmental impact. This paper investigates four clays from deposits in central Germany with the aim of obtaining pozzolans for the production of Portland-pozzolana cement. The results obtained show that the calcined clays possess pozzolanic proper¬ties, which differ depending on calcination temperature and the relative amounts of kaolinite and 2:1 clay minerals. T2 - International Conference on Sustainable Materials, Systems and Structures (SMSS 2019) CY - Rovinj, Croatia DA - 20.03.2019 KW - Blended cements KW - Calcined clays KW - Brick clays KW - Supplementary cementititous materials PY - 2019 N1 - Geburtsname von Priebe, Nsesheye Susan: Msinjili, N. S. - Birth name of Priebe, Nsesheye Susan: Msinjili, N. S. AN - OPUS4-47617 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - One-part alkali-activated materials with high sulfuric acid resistance N2 - Materials with a high acid resistance are required in different important infrastructures. Examples include repair systems for sewer structures, where biogenic sulfuric acid corrosion is the major degradation mechanism. Low-calcium alkali-activated materials (AAMs) have been repeatedly observed to exhibit high acid resistance. However, the reasons for the high acid resistance of these materials were not fully under¬stood until recently, and the use of highly alkaline activator solutions to produce AAMs appears to hamper their commercial uptake. These issues have been tackled by characterising one-part AAMs and studying their alteration when exposed to sulfuric acid. One-part AAMs were synthesized by mixing blends of solid silica and sodium aluminate with water, and subsequent curing at 60–80 °C. Acid resistance testing was performed according to DIN 19573, i.e. exposure to sulfuric acid at pH = 1 for 70 days. Characterisation of the cured and the acid-exposed materials was done by XRD, ATR-FTIR, SEM as well as 29Si, 27Al and 1H MAS NMR spectroscopy, including cross-polarisation and double-resonance methods. Materials synthesized from industrial silicas were gel-zeolite composites, containing a substantial amount of unreacted ‘excess’ silica, while materials synthesized from rice husk ash were fully amorphous, containing ‘excess’ hydrous alumina. The sulfuric acid resistance of mortars based on these binders conformed to the requirements of DIN 19573 for sewer repair applications. The high acid resistance was caused by precipitation of silica gel at the mortar–solution interface, inhibiting further degradation. The presence of alumina gel may inhibit bacterial activity, potentially further improving performance in sewer environments. The phase assemblage of silica/sodium aluminate-based one-part AAMs can be adjusted via choice of the silica starting material. Properly designed materials exhibit excellent acid resistance, caused by precipi¬tation of silica gel which protects subjacent regions, and they may also inhibit bacterial activity. T2 - XVI ECerS Conference CY - Turin, Italy DA - 16.06.2019 KW - Alkali-activated materials KW - One-part mix KW - Acid resistance PY - 2019 AN - OPUS4-48236 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Einkomponentige alkaliaktivierte Bindemittel und Mörtel mit hohem Schwefelsäure-Widerstand N2 - Einkomponentige alkaliaktivierte Bindemittel (AAB), d. h. AAB, bei denen der Aktivator als Feststoff im Bindemittel vorliegt, weisen Vorteile hinsichtlich der praktischen Anwendung im Bauwesen gegenüber konventionellen AAB auf. Einkomponentige AAB lassen sich als Gemische aus reaktiver Silica und Natriumaluminat herstellen, wobei die Reaktionsprodukte von der eingesetzten Silica und den Verhältnissen Na2O/Al2O3/SiO2/H2O abhängen: Während Mikrosilica und ähnliche Reststoffe zu zeolithreichen Produkten führen, erhält man aus Reisschalenasche vollständig amorphe Gele (sog. «Geopolymere»). Mörtel auf Basis solcher Bindemittel entsprechen den Anforderungen von DIN 19573:2016-03 hinsichtlich des Widerstands gegen Schwefelsäureangriff (Prüfung bei pH = 1 für 70 d) und sind damit potentiell als Reparatursysteme für Abwasserinfrastruktur geeignet. Untersuchungen mittels 29Si-MAS-NMR und 1H-29Si-Kreuzpolarisations(CP)-MAS-NMR sowie REM-Aufnahmen von erhärteten und dem Schwefelsäureangriff ausgesetzten AAB zeigen, dass der hohe Säurewiderstand v. a. auf die Fällung von Silicagel an der Grenzfläche Mörtel/Säure zurückzuführen ist, wodurch der Korrosionsfortschritt in darunterliegenden Schichten verlangsamt wird. T2 - Tagung Bauchemie der GDCh-Fachgruppe Bauchemie CY - Aachen, Germany DA - 30.09.2019 KW - Alkaliaktivierte Bindemittel KW - Biogene Schwefelsäurekorrosion KW - Abwasserinfrastruktur KW - Reparatursysteme PY - 2019 AN - OPUS4-49269 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Nachhaltige Betone: Calcinierte Tone als Zementhauptbestandteil N2 - Der Einsatz von calcinierten Tonen als Zementhauptbestandteil ist ein vielversprechender Weg, die mit der Zementherstellung und -verwendung verbundenen CO2-Emissionen zu senken. Im Vortrag werden die Randbedingungen hierfür sowie Ergebnisse eines aktuellen Vorhabens zur Calcinierung von illitreichen Tonen (Ziegeltonen) und anderen Tonen vorgestellt. T2 - Kolloquium Angewandte Geowissenschaften, Technische Universität Berlin CY - Berlin, Germany DA - 14.01.2019 KW - Calcinierte Tone KW - Dreischichtminerale KW - Metakaolin KW - Puzzolane KW - Metatone PY - 2019 N1 - Geburtsname von Priebe, Nsesheye Susan: Msinjili, N. S. - Birth name of Priebe, Nsesheye Susan: Msinjili, N. S. AN - OPUS4-47198 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Strength Development and Characterization of the Reaction of a One-Part-Geopolymer Derived From a Silica Residue and Sodium Aluminate T2 - International Conference on Advances in Cement and Concrete Technology in Africa CY - Johannesburg, South Africa DA - 2013-01-28 PY - 2013 AN - OPUS4-27661 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Geopolymer-bound intumescent coatings for fire protection N2 - Intumescent coatings for fire protection offer advantages over (non-intumescent) cementitious coatings and boards regarding speed of construction, architectural aesthetics, sometimes costs, and other features. However, conventional organic intumescent coatings as well as soluble silicate (waterglass) coatings form foams with low mechanical stability, and the latter coatings generally suffer from low resistance against humidity. Therefore, the search for novel intumescent coatings for more demanding conditions (e.g., abrasive environments) is a necessity in the context of steadily increasing requirements of society and industry. In this contribution, we present results on intumescent aluminosilicate coatings for fire protection that form foams with significantly increased mechanical strength. Two base formulations, a metakaolin/silica-based mix, adapted from Krivenko et al., and a silica/corundum-based mix, developed at Curtin University, as well as formulations modified with additives (Al(OH)3, Mg(OH)2, B2O3, Na2B4O7), were applied to steel plates (75 mm × 75 mm) and exposed to simulated fire conditions (fire curve according to ISO 834-1:1999). Temperature-time curves were recorded to assess the degree at which the coatings insulated the substrate. In addition, XRD, TG, oscillatory rheometry, and SEM were employed to characterise the coatings. The coatings were observed to partly expand during hardening due to H2 formation. When the hardened coatings were exposed to elevated temperatures they intumesced as expected, with the degree and nature of expansion dependent on the formulation. Oscillatory rheometry provided insights into the intumescent processes in an apparently brittle material. It revealed that the hardened aluminosilicate coatings became viscous (loss factor > 1) at 75–225 °C, in the temperature range of major water release, as opposed to a “standard” metakaolin-based geopolymer, which continued to behave as a solid. This explains the intumes¬cent behavior of the coatings, i.e. further expansion and foam formation. Microstructural analysis confirmed pore expansion and coalescence; XRD showed that the phases formed after heating (max. temperature ~840 °C) were of ceramic-type. The fire protection (defined here as the time for the steel substrate to reach the critical temperature of 500 °C) depended mainly on the thick¬ness of the fully expanded coating, i.e. after intumescence. An alumino¬silicate coating free of additives with an original thickness of 12 mm was able to protect the steel for >30 min. The addition of 10 % anhydrous borax (Na2B4O7) caused a significant improvement, such that an original coating thickness of only 6 mm was sufficient to protect the steel for ~30 min. This was caused by the formation of sodium metaborate dihydrate (NaB(OH)4) in the coating that led to a significantly extended dehydration plateau in the temperature-time curve at ~100 °C during the fire exposure. T2 - Alkali Activated Materials and Geopolymers CY - Tomar, Portugal DA - 27.05.2018 KW - Geopolymers KW - Fire protection KW - Fire proofing KW - Intumescence PY - 2018 AN - OPUS4-45088 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Durability-related properties of geopolymer mortars N2 - Knowledge of the durability and related properties of alkali-activated materials is a prerequisite for their application as building materials. However, to date only limited data exists in this regard. The present contribution focuses on durability-related transport properties of geopolymer-based materials. We present results of accelerated carbonation, rapid chloride migration (RCM) and air permeability measurements, together with strength and porosity data, for fly ash-based geoplymers, including formulations containing ground granulated blast furnace slag (GGBFS). It was found that, despite comparable total porosities, the carbonation depths, the chloride migration coefficients and the air permeabilities of the mortars differed significantly. In general, the addition of GGBFS to the binders improved the performance (decreased transport coefficients); however, this was not found to be true for the air permeability in all cases. This latter effect can be explained by drying damage of the C-(A-)S-H gel in GGBFS-containing binders. On the other hand, low transport coefficients can also be achieved by optimization of the binder formulation without the addition of GGBFS, which is also reflected in the material’s air permeability. Thus, there exists no simple correlation between air permeability (of harshly dried mortars) and durability-related transport coefficients for the studied alkali-activated materials. In addition, corrosion potential, polarization resistance data and current density-potential curves of carbon steel in two of the geopolymer mortars are presented. The corrosion potential vs. time curves in combination with polarization resistance values reveal that the steel reinforcement in geopolymer mortars assumed a passive state. However, this happened considerably later than for steel in CEM I-based mortars. T2 - 6th International Conference on Non-Traditional Cement & Concrete (NTCC) CY - Brno, Czech Republic DA - 19.06.2017 KW - Geopolymers KW - Alkali-activated materials KW - Durability KW - Steel corrosion KW - Transport coefficients PY - 2017 AN - OPUS4-41293 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Chemical resistance of hybrid cements against aggressive saline solutions N2 - The safe storage of radioactive material in nuclear waste repositories is a major task of our societies. The sealing function of such repositories is depending on the ability of the applied construction materials to form and maintain a geotechnical barrier with the surrounding rock. Corrosion of the construction material can lead to leakage of radioactive compounds and must therefore be avoided or minimized. Since concretes based on conventional Portland cement have not been found suitable in this context, alternative binders must be evaluated. One such class of binders are hybrid cements, which are blends of low fractions of Portland cement or Portland clinker and high fractions of supplementary cementitious materials, such as blast furnace slag and fly ash, activated by an alkali salt. Besides a low heat of hydration and a sufficient early compressive strength [1], chemical similarities with ancient Roman concrete suggest an excellent durability in saline environments [2], which makes these cements potentially suitable for applications in nuclear waste repositories in evaporite rock, such as the Morsleben repository in Germany. In the present study, two previously designed and characterized [3] hybrid cements, an alkali-activated slag/fly ash blend, and an OPC paste were studied regarding their resistance against corrosion in an aggressive saline solution. The saline solution was designed by the Gesellschaft für Anlagen- und Reaktorsicherheit (GRS) [Association for Facility and Reactor Safety] as a reference representing a solution forming as the result of contact of surface water with evaporite rock. The cement pastes were exposed to the saline solution up to 70 days and characterized by X-ray diffraction, thermogravimetric analysis and spatially resolved X-ray fluorescence spectroscopy. In addition, thermodynamic modelling was performed to simulate the alterations of the phase assemblage with increasing exposure to the saline solution and, thus, provide indications on the long-term durability of the cement pastes. The experimental results revealed a correlation between the Portland clinker content of the cements and the resistance of the cement pastes against attack by the saline solution. This outcome was related to the formation of portlandite when sufficient clinker was available, which maintained the pore solution pH at ~12.5, and thus prevented the dissolution of cementitious phases. Once portlandite was consumed, C-N-A-S-H and ettringite dissolved and released calcium, aluminium, and hydroxide ions in the solution, maintaining the pH at ~10. In this pH range, the formation Cl-AFm phases was observed. At lower pH values, i.e., extended exposure durations, gypsum was the major corrosion product. The pH-dependent dissolution and formation of phases lead to pronounced zonation in the exposed cement pastes. Thermodynamic modelling indicated that the dissolved silicon from C-N-A-S-H reacts with magnesium ions in the saline solution to form M-S-H, and that long-term exposure eventually leads to a material rich in amorphous silica and brucite. T2 - Joint 6th International Workshop on Mechanisms and Modelling of Waste / Cement Interactions & EURAD - WP CORI Workshop CY - Prague, Czech Republic DA - 20.11.2023 KW - Hybrid cement KW - Corrosion KW - Salt solution KW - Magnesium chloride KW - Evaporite rock PY - 2023 AN - OPUS4-58885 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Sulfuric acid resistance of copper-doped and plain metakaolin-based alkali-activated materials studied by 29Si, 27Al and 1H MAS NMR, and Cu K-edge XANES spectroscopy N2 - Alkali-activated materials have been repeatedly reported to exhibit high acid resistance, but no generally accepted hypothesis regarding the underlying mechanisms has emerged yet. To contribute to this issue, K-waterglass-activated metakaolin specimens, with and without the addition of CuSO4·5H2O in the starting mix, were exposed to either a chemically aggressive sewer environment (mortars) or sulfuric acid (pastes). The mode of copper incorporation in the materials and the formation of copper phases in the corroded layers were studied by XANES at the Cu K-edge, and 29Si, 27Al and 1H MAS NMR was employed to understand the processes during acid attack. Copper was found as a spertiniite-like phase in the as-cured materials, while in the deterioration layers of the pastes it was present as copper sulfate. In the corroded regions of the mortars, unequivocal identification of Cu phases was not possible, but the results were reconcilable with the presence of copper carbonate hydroxide. The solid-state NMR results revealed virtually complete dissolution of the K-A-S-H gel and the formation of silica gel, interpreted to be a central mechanism determining the acid resistance. No significant differences between the microstructural alterations of the pastes with and without Cu addition on (chemical) sulfuric acid attack were observed. T2 - 74th RILEM Annual Week & 40th Cement and Concrete Science Conference CY - Online meeting DA - 31.08.2020 KW - Alkali-activated materials KW - Sulfuric acid resistance KW - Sewer structures PY - 2020 AN - OPUS4-51198 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Durlo Tambara, Luís Urbano A1 - Dehn, F. A1 - Gluth, Gregor T1 - Effect of alkali-activated concrete composition on carbonation rate under accelerated and natural conditions N2 - While alkali-activated binders offer certain advantages over traditional Portland cement binders, particu¬larly in terms of resistance against chemical attacks and potentially environmental footprint, their degradation mechanisms remain incompletely understood at present, specifically carbonation. Thus, this study investigates the impact of natural and accelerated carbonation (1% and 4% CO2) on three different compositions of alkali-activated concretes: 100% calcined clay (C100) binder, 100% ground blast furnace slag (S100) binder, and a 40% calcined clay and 60% blast furnace slag blend (C40S60). C100 concretes exhibit faster carbonation kinetics, with five times greater natural carbonation depths than S100. This difference diminishes under accelerated carbonation, showing a 1.5 times difference for 1% CO2 and complete carbonation for 4% CO2 at 90 days. The results thus confirm that accelerated carbonation testing of low-Ca alkali-activated concretes yields results that are not representative of natural carbonation. The C40S60 sample demonstrates a carbonation profile similar to a CEM I concrete, i.e., a high carbonation resistance. Microstructure analysis indicates the formation of three polymorphs of calcium carbonate for S100 (calcite, vaterite, and aragonite), with a higher CO2 concentration favouring aragonite over vaterite. C100 exhibits no calcium carbonates; instead, sodium carbonates form, including trona for 4% CO2 and natrite for both accelerated tests. C40S60 shows calcium and sodium carbonates, although to a lesser extent, containing predominantly calcite and minor signals of natrite. Suitable compositions, like C40S60, prove as effective during natural or accelerated carbonation tests as conventional Portland cement concrete. T2 - RILEM Spring Convention 2024 CY - Milan, Italy DA - 10.04.2024 KW - Alkali-activated concrete KW - Carbonation KW - Calcined clay KW - Slag KW - Durability PY - 2024 AN - OPUS4-59915 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Dauerhaftigkeit von Betonen auf Basis klimafreundlicher Bindemittel N2 - Aus Gründen des Klimaschutzes werden in den kommenden Jahren mehr Zemente mit verringertem Klinkerfaktor und alternative Bindemittel (klimafreundliche Bindemittel) zum Einsatz kommen. Für ihre sichere und zuverlässige Verwendung ist ein umfangreiches Verständnis der Einflüsse auf die Dauerhaftigkeit der aus ihnen hergestellten Betone notwendig. Der vorliegende Beitrag gibt einen kurzen Überblick über einige jüngere Entwicklungen und Forschungsergebnisse auf dem Gebiet. Der Fokus liegt auf Ergebnissen der Arbeiten von Technischen Komitees der RILEM sowie der EFC und eigenen Forschungsergebnissen. T2 - 11. Jahrestagung des DAfStb mit 63. Forschungskolloquium der BAM Green Intelligent Building CY - Berlin, Germany DA - 16.10.2024 KW - Beton KW - Bindemittel KW - Klimaschonender Zement KW - Bewehrungskorrosion KW - Chlorideindringen KW - Carbonatisierung PY - 2024 AN - OPUS4-61816 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - RILEM TC 281-CCC WG6 - Carbonation of alkali-activated concrete: preliminary results N2 - Preliminary results of RILEM TC 281-CCC Working Group 6 'Carbonation of alkali-activated concrete' are presented. T2 - 74th RILEM Annual Week & 40th Cement and Concrete Science Conference CY - Online meeting DA - 31.08.2020 KW - Alkali-activated materials KW - Carbonation PY - 2020 AN - OPUS4-51199 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 - CONF A1 - Gluth, Gregor T1 - Corrosion of steel reinforcement in geopolymer mortars - carbonation resistance, chloride migration, and preliminary corrosion potential data N2 - Alkali-activated materials such as geopolymers are currently receiving a lot of attention because of their potential to be used as binders for concrete with advantageous engineering properties and reduced manufacturing CO2 emissions. Knowledge of the durability of steel in these concretes and related properties of alkali-activated materials is a prerequisite for their application as building materials, if they are to be used for steel reinforced elements. However, to date only limited data exists on this topic. The present contribution focuses on durability-related transport properties of geopolymer-based mortars (as model systems for concrete). We report results of accelerated carbonation, rapid chloride migration (RCM) and air permeability measurements as well as porosity data for fly ash-based geopolymer mortars, including mixes containing ground granulated blast furnace slag (GGBFS). In addition, we report polarization resistance data and corrosion potential vs. time curves for carbon steel bars embedded in two of the fly ash-based geopolymer mortars and a CEM I-based mortar (as reference). Despite comparable total porosities, the carbonation depths, the chloride migration coefficients and the air permeabilities of the mortars differed significantly. In general, the addition of GGBFS to the binders improved the performance (decreased transport coefficients); however, this was not found to be true for the air permeability in all cases. This latter effect can be explained by drying damage of the C-(A-)S-H gel in GGBFS-containing binders. On the other hand, low transport coefficients can also be achieved by optimization of the binder formulation without the addition of GGBFS, which is also reflected in the material’s air permeability. Thus, there exists no simple correlation between air permeability (of harshly dried mortars) and durability-related transport coefficients for the studied alkali-activated materials. The corrosion potential vs. time curves in combination with polarization resistance values reveal that the steel reinforcement in geopolymer mortars assumed a passive state. However, this happened considerably later than for steel in CEM I-based mortars. The free corrosion potential of carbon steel reinforcement in the geopolymer mortars had different values than the free corrosion potential values for the CEM I-based mortar for both the active and the passive state; possible reasons for this behavior are discussed. T2 - EUROCORR 2017 CY - Prague, Czech Republic DA - 03.09.2017 KW - Geopolymers KW - Alkali-activated materials KW - Corrosion KW - Steel reinforcement KW - Concrete PY - 2017 AN - OPUS4-41869 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Corrosion of steel in geopolymer mortars N2 - The contribution reports on durability-related transport properties of geopolymer-based mortars. We show results of accelerated carbonation, rapid chloride migration (RCM), accelerated chloride diffusion, and air permeability measurements for fly ash-based geopolymer mortars, including mixes containing ground granulated blast furnace slag (GGBFS). In addition, we report polarization resistance data and corrosion potential vs. time curves for carbon steel bars embedded in two of the fly ash-based geopolymer mortars and a CEM I-based mortar (as reference). Despite comparable total porosities, the carbonation depths, the chloride migration coefficients and the air permeabilities of the mortars differed significantly. In general, the addition of GGBFS to the binders improved the performance (decreased transport coefficients); however, this was not found to be true for the air permeability in all cases. This latter effect can be explained by drying damage of the C-(A-)S-H gel in GGBFS-containing binders. On the other hand, low transport coefficients can also be achieved by optimization of the binder formulation without the addition of GGBFS, which is also reflected in the material’s air permeability. The corrosion potential vs. time curves in combination with polarization resistance values reveal that the steel reinforcement in geopolymer mortars assumed a passive state. However, this happened considerably later than for steel in CEM I-based mortars. The free corrosion potential of carbon steel reinforcement in the geopolymer mortars had different values than the free corrosion potential values for the CEM I-based mortar for both the active and the passive state. T2 - International Workshop on Alkali-Activated Materials CY - Ljubljana, Slovenia DA - 11.05.2017 KW - Geopolymers KW - Alkali-activated materials KW - Reinforcement corrosion KW - Carbonation KW - Chloride ingress PY - 2017 AN - OPUS4-40241 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Vergleich unterschiedlicher Verfahren zur Messung der Oberflächenrauheit T2 - 7. Internationales Kolloquium Industrieböden CY - Ostfildern, Germany DA - 2010-12-14 PY - 2010 AN - OPUS4-22795 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - LightSHIP II - Inorganic Binder System for Innovative Panel Technology in East Africa T2 - Africa Re:Load/Discover new opportunities for innovation and business, öffentlicher Workshop CY - Weimar, Germany DA - 2011-08-29 PY - 2011 AN - OPUS4-24471 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - LightSHIP II: Inorganic Binder Systems for Innovative Panel Technology in East Africa T2 - Workshop Cement and Concrete for Africa CY - Berlin, Germany DA - 2011-08-17 PY - 2011 AN - OPUS4-24725 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Chloride binding by LDH/AFm phases and alkali-activated slag pastes N2 - Chloride binding by the hydrate phases of cementitious materials influences the rate of chloride ingress into these materials and, thus, the time at which chloride reaches the steel reinforcement in concrete structures. A particularly important role in this context is played by layered double hydroxides (LDHs), including AFm phases. Chloride binding isotherms of individual LDH/AFm phases would be required as input for computational models of chloride ingress, but such isotherms are only available for a few AFm phases, and in addition the available data are partly conflicting. The present study, conducted in the context of RILEM TC 283-CAM ‘Chloride transport in alkali-activated materials’, significantly extends the available database by determining the chloride binding isotherms of LDH/AFm phases (monosulfate, strätlingite, hydrotalcite, and meixnerite), and of alkali-activated slags (AAS) produced with four different activators (Na2SiO3, Na2O∙1.87SiO2, Na2CO3, and Na2SO4), in NaOH/NaCl solutions at various liquid/solid ratios. Selected solids after chloride binding were analysed by X-ray diffraction, and thermodynamic modelling was applied to simulate the phase changes occurring during chloride binding by the AFm phases. The chloride binding isotherms of LDH/AFm phases depended strongly on the liquid/solid ratio during the experiments, resolving apparent contradictions of the previously available data. The dependency on liquid/solid ratio must be attributed to kinetic restrictions, which are, however, currently poorly understood. Chloride binding by AAS pastes was generally higher than for Portland cement pastes and was only moderately influenced by the employed activator. A steep increase of the chloride binding by AAS occurred at free chloride concentrations above approx. 1.0 M, which is possibly related to chloride binding by the C-(N-)A-S-H gel in the AAS. T2 - RILEM Spring Convention 2024 & Conference on Advanced Construction Materials and Processes for a Carbon Neutral Society CY - Milan, Italy DA - 07.04.2024 KW - Chloride binding KW - Layered double hydroxides KW - AFm phases KW - Alkali-activated slags KW - Chloride sorption isotherms PY - 2024 AN - OPUS4-59855 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Thermo-mechanical and spalling behavior of normal weight and lightweight geopolymer concretes N2 - The mechanical and microstructural properties of two geopolymer concretes, produced with either quartz aggregate or expanded clay aggregate, were assessed before, during and after high-temperature exposure up to 750 °C in order to better understand the engineering properties of the material. SEM investigations were also undertaken to better understand the observed changes in the mechanical properties. It was found that dehydration of capillary water caused micro-cracking and strength losses at temperatures ≤ 300 °C. At higher temperatures (T ≥ 500 °C) sintering promoted strength increases, leading significant strength advantages over conventional concretes. Stress-mechanical strain curves, which are the basis of the fire design of concrete structures, were determined. In addition, the two geopolymer concretes where exposed to the ISO 834-1 standard fire curve in a small-scale spalling test set-up. Acoustic emission measurements during, and acoustic measurements and optical microscopy after heat exposure were employed to investigate crack formation during the tests. Both concretes did not spall, which is attributed to their comparatively high permeability and their low amount of chemically bound water. Significant crack formation was detected only around the temperature of the α–β quartz transition (573 °C) and on cooling. Because of aggregate deformations at the quartz transition temperature, deterioration after heating was more significant in the geopolymer concrete with quartz aggregates. Crack formation occurred also in the concrete with expanded clay aggregates, presumably caused by shrinkage of the geopolymer paste on cooling. T2 - Advances in Cement and Concrete Technology in Africa (ACCTA 2016) CY - Dar es Salaam, Tanzania DA - 27.01.2016 KW - Geopolymers KW - Concrete KW - Transient thermal creep KW - Spalling KW - Heat exposure PY - 2016 AN - OPUS4-36922 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Alkalisch aktivierte Bindemittel mit hohem Säurewiderstand für die Kanalsanierung N2 - Die biogene Schwefelsäurekorrosion (BSK) von Betonbauteilen in Abwassersystemen verursacht weltweit hohen Reparaturbedarf. Um zukünftigen Reparaturbedarf zu minimieren, werden für Neubau- und Sanierungsmaßnahmen z. T. Materialien mit besonders hohem Widerstand gegen BSK benötigt. Der vorliegende Beitrag beschreibt Forschungen zu alkalisch aktivierten Bindemitteln, die bei geeigneter Formulierung einen hohen Widerstand gegen BSK bzw. Säureangriff aufweisen. Zusätzlich werden jüngste Fortschritte bei der Bewertung von Methoden zur Prüfung des Widerstands gegen BSK dargestellt. T2 - 11. Jahrestagung des DAfStb mit 63. Forschungskolloquium der BAM Green Intelligent Building CY - Berlin, Germany DA - 16.10.2024 KW - Alkalisch aktivierte Bindemittel KW - Biogene Schwefelsäurekorrosion KW - Säurewiderstand PY - 2024 AN - OPUS4-61747 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Geopolymers - Novel low-calcium cements T2 - International Conference on Advances in Cement and Concrete Technology in Africa - Pre Conference Workshop CY - Johannesburg, South Africa DA - 2013-01-25 PY - 2013 AN - OPUS4-27662 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Reinforcing steel in sulfide-containing concretes – corroding or not corroding? N2 - Blast furnace cements (CEM III) and alkali-activated slags are binders for concretes with several advantageous engineering properties, and their increased adoption in construction industry could contribute to reducing the CO2 emissions associated with cement production and use. However, the current knowledge about how these cements protect steel reinforcement in concretes against corrosion is very incomplete, which impedes their large-scale application. This knowledge gap is mainly due to the fact that these cements release sulfide and other reduced sulfur species into the concrete pore solution, the consequences of which for the state of the reinforcement and electrochemical measurements are not fully understood. The present contribution first describes peculiarities of electrochemical measurements of steel in sulfide-containing cementitious materials and related solutions as reported in the literature and a recent report by EFC Working Party 11. It is demonstrated that the high sulfide concentrations in these systems lead to low open circuit potentials and low polarisation resistances, which may be incorrectly interpreted as indicating active corrosion of the steel. Second, preliminary results of an ongoing project [funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – 458297195] related to the passivation and corrosion initiation of steel in sulfide-containing solutions and mortars are presented. Eight mortars based on one alkali-activated blast furnace slag (BFS), three alkali-activated BFS/fly ash blends, one sodium sulfate-activated CEM III/C (‘hybrid cement’), one CEM III/C, one CEM III/B, and one CEM I (ordinary Portland cement, OPC) were produced, and their pore solutions expressed and analysed after 7, 14, 28, and 56 days of curing. The pH values of the solutions differed systematically, with the highest pH values recorded for the CEM I and the alkali-activated BFS/fly ash blends with a high proportion of fly ash, and the lowest pH recorded for the CEM III/B. The redox potentials of the solutions were between −500 mV and −340 mV vs. Ag/AgCl for the alkali-activated binders, approx. +10 mV vs. Ag/AgCl for the CEM I, and in between for the CEM III/B and the CEM III/C. As expected, the electrical conductivity was highest for the alkali-activated binders. These results are explained by the chemical compositions of the pore solutions of the mortars. Finally, a test set-up to investigate the behaviour of steel in sulfide-containing solutions and the changes on subsequent oxygen and/or chloride addition is introduced. Preliminary electrochemical measurements of steel in sulfide-containing solutions are presented and discussed in the context of the above-mentioned data from the literature and the compositions of the pore solutions of the studied mortars. T2 - 7th Swiss Corrosion Science Day 2023 CY - Zurich, Switzerland DA - 24.04.2023 KW - Reinforcing steel KW - Sulfide KW - Concrete KW - Ground granulated blast furnace slag KW - Corrosion PY - 2023 AN - OPUS4-57386 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - One-part geopolymers and geopolymer-zeolite composites based on silica: factors influencing microstructure and engineering properties N2 - Mixing and curing of geopolymers and related alkali-activated materials without storage and handling of highly alkaline solutions possesses advantages regarding safety and economic viability; one possible approach is to produce these materials from solid silica feedstocks and solid sodium aluminate, and subsequent mixing with water. We present a comparison between geopolymers and geopolymer-zeolite composites synthesized by this route from different silica feedstocks (by-product silica from chlorosilane production, microsilica, rice husk ash) and with different SiO2/Al2O3 ratios, using results from XRD, NMR, SEM, thermal analysis, mechanical and acid resistance testing. The use of rice husk ash favors formation of a fully amorphous geopolymer with high strength. Utilization of the other silica feedstocks leads to formation of geopolymer-zeolite composites, the amount and kind of zeolites depending on the feedstock and the SiO2/Al2O3 ratio. These composites show beneficial dehydration behavior, viz. no distinct dehydration step of thermal strain, with the phase assemblage after heating to 1000 °C controlled by the starting composition. Mortars produced from both, the geopolymers as well as the compo¬sites, exhibit high resistance to sulfuric acid attack, making them promising materials for the construction and the repair of industrial and sewer structures. T2 - 42nd International Conference and Expo on Advanced Ceramics and Composites CY - Daytona Beach, FL, USA DA - 21.01.2018 KW - Alkali-activated materials KW - Geopolymers KW - Acid resistance KW - High-temperature resistance PY - 2018 AN - OPUS4-44145 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Geopolymerisation kieselsäurehaltiger Rückstände aus der Reststoffaufbereitung der Chlorosilanproduktion T2 - 18. Internationale Baustofftagung (IBAUSIL) CY - Weimar, Germany DA - 2012-09-12 PY - 2012 AN - OPUS4-26556 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Structure, acid resistance and high-temperature behavior of silica-based one-part AAMs N2 - One-part geopolymers (OPGs) are a sort of alkali-activated materials (AAMs) which production avoids the use of highly-alkaline activator-solutions and contributes to a better acceptance of alternative mineral binders in terms of safety-related and economic aspects. In the present contribution OPGs were synthesized by blending silica sources (two industrial silicas and two biogenic silicas) with sodium aluminate and only water must be added to initiate the hardening, i.e. mixing is performed in the same way as for conventional Portland cements. The OPGs were characterized by XRD, and SEM and the degrees of reaction of the silicas were determined by a chemical dissolution method. The industrial silicas led to the formation of geopolymer-zeolite composites, that contained, besides geopolymeric gel, crystalline tectosilicates (e.g. zeolite A and hydrosodalite) and depending on the starting composition also unreacted silica. The biogenic silicas provided a higher reactivity and avoided the formation of crystallite by-products. The differences in the microstructures caused differences in the mechanical strength of the specimens. The treatment of the OPG composites at moderate elevated temperatures revealed promising behavior on thermal dehydration in terms of shrinkage and residual strength up to 700 °C. Above 700 °C sintering and partial melting occurred, and new phase formation commenced. After exposure to 1000 °C the specimens appeared virtually amorphous or formed stuffed silica structures of nepheline- or carnegieite-type type. The investigations of the OPG based mortars on their resistance against sulfuric acid in accordance with DIN 19573 (Appendix A) revealed very high residual strengths up to 78 % after treatment with H2SO4 (pH 1) for 70d. A mechanism of dissolution of the primary aluminosilicate reaction products of the pastes and the precipitation of a silica gel that protects the remaining aluminosilicates and decelerates further corrosion was found to be the main reason for the good performance under acidic conditions. The addition of CaO-containing feedstocks enhanced hardening, but at a certain content the resistance against sulfuric acid decreased, due to the formation of gypsum on exposure to sulfate. In addition, the mortars exhibited excellent shrinkage behavior as well as good bond to concrete substrates with pull-off strength up to > 3 MPa. The workability of the fresh mortars provided very good manual applicability; automatic applications such as sprayed and spun mortars will require further optimization regarding rheological properties. In summary, the studied OPG are promising materials for the construction and the repair of concrete structures, such as sewers, that are affected by biogenic sulfuric acid corrosion. T2 - Alkali Activated Materials and Geopolymers CY - Tomar, Portugal DA - 27.05.2018 KW - Alkali-activated materials KW - Geopolymers KW - Acid resistance KW - Solid state NMR PY - 2018 AN - OPUS4-45087 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Design and Characterization of Fly Ash-Based Geopolymer Concretes for a Round Robin Durability Testing Program T2 - Geopolymers: The route to eliminate waste and emissions in ceramic and cement manufacturing CY - Hernstein, Austria DA - 2015-05-24 PY - 2015 AN - OPUS4-33513 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Inhalt der Verordnungen für Heizungsanlagen - Überblick N2 - Seit dem 26.09.2015 gelten in Deutschland Anforderungen an die umweltgerechte Gestaltung und die Energiekennzeichnung von Heizgeräten und Verbundanlagen mit Heizgeräten. Der Vortrag stellt die zugrundeliegenden EU-Verordnungen und die sich ergebenden Konsequenzen überblicksmäßig vor. T2 - Kolloquium Marktüberwachung im Bereich Heizungsanlagen CY - Berlin, Germany DA - 06.04.2016 KW - Heizgeräte KW - Verbundanlagen KW - Umweltgerechte Gestaltung KW - Ökodesign KW - Energieverbrauchskennzeichnung PY - 2016 AN - OPUS4-36924 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Influence of sodium concentrations of the activating solution on the hydration of calcium carbonate-rich wastepaper sludge ash T2 - 5th International Conference on Non-Traditional Cement & Concrete CY - Brno, Czech Republic DA - 2014-06-16 PY - 2014 AN - OPUS4-33514 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Structural Investigations n One-Part Geopolymers after Different Drying Regimes T2 - 34th Cement & Concrete Science Conference CY - Sheffield, England DA - 2014-09-14 PY - 2014 AN - OPUS4-33516 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Hydration and strength development of calcite-rich wastepaper sludge ash T2 - Concrete Innovation Conference - CIC 2014 CY - Oslo, Norway DA - 2014-06-11 PY - 2014 AN - OPUS4-33515 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Energieverbrauchskennzeichnung: Aktivitäten von BAM, UBA und dena T2 - Auftaktveranstaltung - Deutsche Akteursplattform Solarthermie-Labeling CY - Frankfurt/Main DA - 2015-07-06 PY - 2015 AN - OPUS4-33701 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gluth, Gregor T1 - Inhalt der neuen Verordnungen für Heizungstechnik T2 - Informationsveranstaltung Ökodesign und Energieverbrauchskennzeichnung von Heizgeräten CY - Berlin, Deutschland DA - 2015-09-09 PY - 2015 AN - OPUS4-35244 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -