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The corrosion behavior of galvanized steels and zinc components under atmospheric exposure depends mostly on the corrosion product‐based cover layer formation under the prevailing conditions. The use of agar‐based gel electrolytes makes it possible to use electrochemical methods to obtain a characteristic value from these cover layers that describe their current and future protective capacity. It is shown here that different states of galvanized steel can be distinguished very well under laboratory conditions and that this method is also suitable for use under practical conditions. Based on the characteristic values and assuming future time of wetness, it is very easy to draw up a forecast for the future corrosion rate, which provides plausible values. [ABSTRACT FROM AUTHOR]

Corrosion monitoring of reinforced or prestressed concrete structures has become increasingly important in recent years. Areas of application include components that are no longer accessible after completion or where potential field measurements cannot be carried out due to existing coatings. Corrosion monitoring can also be used to monitor the progress of corrosion in corroding systems, e.g. to prove the success of repair measures according to repair principle 8 in accordance with EN 1504‐9 or repair method 8.3 in accordance with the DIBt repair guideline. It also could be used to prove the functionality of cathodic corrosion protection systems in accordance with ISO 12696. Despite the increasing importance of corrosion monitoring, no guidelines or recommendations existed until 2018. This gap was closed by the English version of specification B12, "Corrosion Monitoring of Reinforced and Prestressed Concrete Structures," of the German Society for Non‐Destructive Testing, which was published in 2021. This article introduces specification B12 by explaining the basic measurement principles and illustrating the potential of corrosion monitoring in new and existing buildings. [ABSTRACT FROM AUTHOR]

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The critical chloride content Ccrit is an indicator of the corrosion resistance of reinforcing steels in concrete. In this article, several experimental methods for determining the critical chloride content Ccrit of mild and alloyed (12% Cr) steel in cementitious materials are compared. The methods used include accelerated polarization tests and tests employing more natural (unpolarized) conditions in which chloride ingress occurs by diffusion and capillary uptake. The advantages and disadvantages of the methods are discussed, in particular, against the objective of reaching a compromise between applicability to practice and feasibility in laboratory testing. [ABSTRACT FROM AUTHOR]

Copyright of Bautechnik is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The critical chloride content Ccrit is an indicator of the corrosion resistance of reinforcing steels in concrete. In this article, several experimental methods for determining the critical chloride content Ccrit of mild and alloyed (12% Cr) steel in cementitious materials are compared. The methods used include accelerated polarization tests and tests employing more natural (unpolarized) conditions in which chloride ingress occurs by diffusion and capillary uptake. The advantages and disadvantages of the methods are discussed, in particular, against the objective of reaching a compromise between applicability to practice and feasibility in laboratory testing. [ABSTRACT FROM AUTHOR]

Risk of hydrogen evolution on martensitic screw anchors under practical construction conditions The present investigation deals with the question of whether the formation of hydrogen is possible on fully martensitic screw anchors under practical conditions. In contrast to austenitic materials, martensitic steels always have the possibility of hydrogen‐induced embrittlement of the material in the presence of hydrogen. For this purpose, a scenario was chosen which is frequently encountered in practice and which comprises a galvanic element consisting of stainless screw anchors (in this case martensitic) and a galvanized anchor plate on a concrete body. The element current between the components as well as the corrosion potential are recorded to prove hydrogen development. The results of the tests show that a strong cathodic polarization of the martensitic screw anchors occurs over a limited period due to the corrosive dissolution of the zinc. As a result, water decomposition occurs in the phase boundary area of the screw anchors and atomic hydrogen is formed. The calculated gas volume of the resulting hydrogen at the steel anchors was determined and was 11.14 ± 1.94 ml on average. Diffusion of the hydrogen adsorbed on the steel surface into the martensitic material is thus theoretically possible and implies a possible risk of hydrogen‐induced crack formation and spontaneous failure under load. [ABSTRACT FROM AUTHOR]

Chloride contents at the steel–mortar interface that initiate steel corrosion were determined for carbon steel in alkali‐activated fly ash mortar for three different exposure conditions: exposure to 1 M NaCl solution; leaching in deionized water and then exposure to 1 M NaCl solution; and leaching in deionized water, aging in air at 20°C and natural CO2 concentration, and then exposure to 1 M NaCl solution. For comparison, a Portland cement mortar, exposed to 1 M NaCl solution, was studied. The median values of the corrosion‐initiating chloride contents (average over the full length of the rebar) in the alkali‐activated fly ash mortar varied between 0.35 and 1.05 wt% Cl with respect to binder, consistently lower than what was obtained for the Portland cement mortar, but with no clear trend regarding the exposure conditions. For most of the alkali‐activated fly ash mortar specimens, preferential corrosion at the connection between the working electrode and the external measurement setup was observed, while preferential corrosion did not occur for the Portland cement mortar. Scanning electron microscopy and auxiliary experiments in synthetic solutions indicated that this behavior was caused by inhomogeneities at the steel–mortar interface in the alkali‐activated mortar, likely due to its peculiar rheological properties in the fresh state. [ABSTRACT FROM AUTHOR]

Determination of the corrosion‐inducing chloride content of stainless ferritic reinforcing steels in mortar The corrosion protection mechanism for stainless steel in concrete is different than for unalloyed steel. In carbonated concrete, stainless steels are in a passive state and do not have any uniform corrosion. The chloride content for the initiation of pitting corrosion on stainless steels in concrete depends not only on the content of alloying elements (above all chromium) and the surface condition. It also depends on the concentration ratio between OH– and Cl– in the electrolyte. It can be expected that lower chloride contents can initiate corrosion in carbonated concretes than in concretes with higher pH values. This ap‐plies especially to stainless steel with low chromium contents such as products made of the material 1.4003 (X2CrNi12). In order to determine the critical corrosion‐inducing chloride content using the example of a pickled ferritic chromium steel available on the market, extensive laboratory tests were carried out at the Federal Institute for Materials Research and Testing (BAM). In accelerated corrosion tests in alkaline and carbonated mortars, the critical chloride contents in the phase boundary between reinforcing steel and mortar were determined and evaluated by means of laser induced breakdown spectroscopy (LIBS). [ABSTRACT FROM AUTHOR]

Copyright of Bautechnik is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Beton- Und Stahlbetonbau is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Tests for assessing prestressing steels' susceptibility to hydrogen‐induced stress corrosion cracking are essential for approvals, in‐house monitoring, and third‐party material testing. According to ISO 15630‐3, the time to brittle fracture by constant load under corrosive conditions in thiocyanate test solutions (A or B) at 50°C is measured. In the literature, a high scattering in stress corrosion tests is reported, which questions the integrity of the test procedure. This paper shows the results of studies about the influence of solution composition on hydrogen charging in electrochemical and permeation measurements. Electrochemical experiments show that polished steel surfaces without common drawing layers have more consistent free corrosion currents, polarization resistances, and B‐values in solution A with low scattering compared to the solution B experiments. The influence of temperature at 50°C and an ambient temperature of 22°C was also tested. [ABSTRACT FROM AUTHOR]