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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.
Two design approaches for multifunctional information carriers are introduced. In the first one, quick response (QR) code carriers, which were composed of poly(ester urethane) (PEU) and microencapsulated thermochromic pigments (T-PIGs), differing in color and color switching temperature (CST), were prepared. The obtained material systems exhibited machine-readable QR codes at 23 °C and a two-stage decolorization when heated, culminating in unreadable QR codes at temperatures above the highest CST of the employed T-PIGs. In the second scenario, information carriers were sealed with a dark, thermochromic PEU layer. As a result, the QR codes were hidden at 23 °C and became readable upon heating due to color fading. Beyond the characterization of the employed components, preparation methods, functionality analyses and durability investigations are reported. When heated after thermo-mechanical programming, pronounced shape memory properties could be verified. The thermo-responsiveness of such multifunctional material systems may qualify them for usage in anti-counterfeiting applications.
We report the selective ring opening copolymerisation (ROCOP) of
oxetane and phthalic thioanhydride by a heterobimetallic Cr(III)K
catalyst precisely yielding semi-crystalline alternating poly(esteralt-
thioesters) which show improved degradability due to the
thioester links in the polymer backbone.
Many standardised durability testing methods have been developed for Portland cement-based concretes, but require validation to determine whether they are also applicable to alkali-activated materials. To address this question, RILEM TC 247-DTA ‘Durability Testing of Alkali-Activated Materials’ carried out round robin testing of carbonation and chloride penetration test methods, applied to five different alkali-activated concretes based on fly ash, blast furnace slag or metakaolin. The methods appeared overall to demonstrate an intrinsic precision comparable to their precision when applied to conventional concretes. The ranking of test outcomes for pairs of concretes of similar binder chemistry was satisfactory, but rankings were not always reliable when comparing alkali-activated concretes based on different precursors. Accelerated carbonation testing gave similar results for fly ash-based and blast furnace slag-based alkali-activated concretes, whereas natural carbonation testing did not. Carbonation of concrete specimens was observed to have occurred already during curing, which has implications for extrapolation of carbonation testing results to longer service life periods. Accelerated chloride penetration testing according to NT BUILD 443 ranked the tested concretes consistently, while this was not the case for the rapid chloride migration test. Both of these chloride penetration testing methods exhibited comparatively low precision when applied to blast furnace slag-based concretes which are more resistant to chloride ingress than the other materials tested.
The current understanding of the carbonation and the prediction of the carbonation rate of alkali-activated concretes is complicated inter alia by the wide range of binder chemistries used and testing conditions adopted. To overcome some of the limitations of individual studies and to identify general correlations between mix design parameters and carbonation resistance, the RILEM TC 281-CCC ‘Carbonation of Concrete with Supplementary Cementitious Materials’ Working Group 6 compiled and analysed carbonation data for alkali-activated concretes and mortars from the literature. For comparison purposes, data for blended Portland cement-based concretes with a high percentage of SCMs (≥ 66% of the binder) were also included in the database. The analysis indicates that water/CaO ratio and water/binder ratio exert an influence on the carbonation resistance of alkali-activated concretes; however, these parameters are not good indicators of the carbonation resistance when considered individually. A better indicator of the carbonation resistance of alkali-activated concretes under conditions approximating natural carbonation appears to be their water/(CaO + MgOeq + Na2Oeq + K2Oeq) ratio, where the subscript ‘eq’ indicates an equivalent amount based on molar masses. Nevertheless, this ratio can serve as approximate indicator at best, as other parameters also affect the carbonation resistance of alkali-activated concretes. In addition, the analysis of the database points to peculiarities of accelerated tests using elevated CO2 concentrations for low-Ca alkali-activated concretes, indicating that even at the relatively modest concentration of 1% CO2, accelerated testing may lead to inaccurate predictions of the carbonation resistance under natural exposure conditions.
For almost 15 years, carbon fibre-reinforced polymer (CFRP) plates and sheets have been used for strengthening and repair of civil engineering structures. CFRP plates were applied to upgrade structures for change in use or increasing traffic load. CFRP laminates have also been used to repair deteriorated structures such as multi-storey parking or bridges. The execution quality and condition of the strengthening measure in terms of bond integrity were neither monitored nor tested systematically. Inspectors eventually applied simple hammer knocking during regular main inspection for subjective noise distinction as a measure for eventual insufficient bond. This paper presents the feasibility and the limitations of low-frequency transversal ultrasonic waves with dry-coupling point-contact sensors for inspection and defect detection between CFRP laminate and concrete surfaces. The German Centre of Competence in Civil Engineering (DIBt) has initiated a national research project [Helmerich et al. (2012). Condition analysis of bonded CFRP-applications on concrete structures by means of non-destructive testing [in German: Zustandsuntersuchung von CFK-Klebeverstärkungen an Betonbauteilen mittels zerstörungsfreier Prüfung (ZfP)]. Final, internal project report], carried out at the Federal Institute for Materials Research and Testing (BAM), Germany. The aim of the project was to present a potential non-destructive testing method for bond defect detection as a measure for the durability of the strengthening system more than 10 years after application.
The paper presents the results of a study dealing with the performance of water repellents on hardened blended cement pastes. Since on the European market Portland cement does not play the dominant role anymore and due to the new national and European policies concerning Greenhouse Gases and sustainability, cement manufacturers produce more and more blended cements (CEM IICEM V). Nevertheless, the majority of experience concerning the efficacy of water repellents is gained from Portland cement; therefore knowledge in regard to the interactions of blended cement with water repellent agent is minimal. Two silane-based products were applied on 'fresh' and carbonated cement substrates containing limestone, fly ash, slag and trass, and were investigated in terms of their functionality. The evaluation of the treatments' performance and effectiveness were assessed using various laboratory measurements. Hydrophobicity, water absorption, colour changes and the penetration depth of silanes into the substrate were evaluated before and after artificial aging experiments. Moreover, the outdoor weathering test was performed to shed light on treated surface appearance in a 'real' outdoor environment. The results showed that surface wettability was independent on water ingress or colour variations, especially for cement specimens artificially aged by accelerated carbonation. Cement pastes containing slag and trass seemed to more distinctly affect the water repellents' surface performance.
The service-life of steel-reinforced concrete structures is primarily determined by the ability of the concrete cover to resist chloride ingress. With limited literature available on the ingress of chloride into alkali-activated slags (AAS) under service conditions, it is critical that this is described by appropriate models. This paper describes an interactive software framework to relate chloride ingress into AAS with the chemistry of the concrete cover, by considering the chloride binding capacity and porosity of the binder as a function of time, based on thermodynamic calculations of the phase assemblage as a function of slag and activator composition. This provides a major step towards developing the ability to predict the ingress of chlorides in alkali-activated concretes from a sound theoretical basis, which is essential in providing confidence in the durability of these materials in essential infrastructure applications.
The interaction of municipal solid waste incinerator bottom ash (MSWI bottom ash), when utilized as an aggregate in concrete, with the cement matrix was investigated. The most prominent reaction observed in lab and field concrete was the formation of aluminium hydroxide and the release of hydrogen gas from aluminium grains reacting in the alkaline environment. The expansive aluminium reaction was identified as a main cause of extensive spalling on the concrete surface. Due to the higher content of bottle glass as part of the ash, in all samples, reaction products of an alkali-silica reaction (ASR) could be observed as well. However, damage due to ASR were less severe than those caused by the aluminium reaction. The expansion rates were low and only a few of the lab samples showed cracking. Microstructural analysis of the samples indicated clearly that a large quantity of the alkali-silica gel which was formed was accommodated in the pores and voids without exerting any strain on the material.
Data are reported from oven aging in circulating air and water immersion tests at 80°C on various polyolefin (polyethylene (PE) and polypropylene (PP)) needle-punched nonwoven geotextiles (GTnws) and the results of these long-term tests are compared with the oxidative resistance of high-density PE geomembranes (HDPE GMs) described in a preceding paper (Polym. Degr. Stability 79(1) (2003) 161). Polyolefin fibers used in geotextiles are typically less stabilized, have a very high surface-to-volume ratio and an oriented morphology compared with HDPE GMs. Therefore, significant differences in the oxidation behavior of these products are expected which may affect their durability. Two general results can be obtained from our measurements: Firstly, while the lifetime of the HDPE GM is essentially determined by the slow loss of stabilizers, for all GTnws a rapid reduction in the oxidative induction time (OIT) and, as we conclude, in the amount of stabilizer was observed during water immersion and air aging. Secondly, the mechanical property degradation of the GTnws depended strongly on the oxidation conditions: the induction period prior to the degradation was much longer for immersion in water than for oven aging in circulating air. After antioxidant depletion, an induction time of the oxidation reaction, which depends on the draw ratio of the stretched fibers and the oxygen supply, might substantially contribute to the induction period of the mechanical property degradation of GTnws. For one PP GTnw product, a sudden reduction in the mechanical strength occurred after onset of degradation which continued rapidly until complete deterioration. For other PP samples as well as for all PE GTnws the reduction in mechanical strength proceeded slowly. Best fits were obtained by modeling the degradation process of the PE GTnws by a second-order kinetic. Using an activation energy of 60 kJ/mol (Geotextiles, Geomembranes and Related Products, Balkema, Rotterdam, 1990; Conference Proceedings of the Sixth International Conference on Geosynthetics, Industrial Fabrics Association International (IFAI), Atlanta, USA, 1998, pp. 683690; Clay Geosynthetic Barriers, Balkema, Lisse, The Netherlands, 2002, pp. 8796), lower limits of the half-live of the degradation at worst case field conditions were obtained in the range 3083 years. Some decades have to be added for the overall induction time. However, under field conditions with limited oxygen supply, the expected service lifetime might be at least half an order of magnitude longer.