Academic literature on the topic 'Concrete pore solution'

Three epoxy-coated reinforcing steel (ECR) types removed from job sites, one shipped directly from the coater's plant, three commercial corrosion inhibitors, and one ECR plus a corrosion inhibitor were evaluated as reinforcing steel corrosion protection systems against chloride induced corrosion. The three corrosion inhibitors were calcium nitrite, an aqueous mixture of esters and amines, and a mixture of alcohol and amine. The ECR was tested in two groups, 0% and 1% coating damage. Corrosion protection performance was evaluated by the amount of visually observed blister surface area, for the ECR, and corroded surface area, for the tested corrosion inhibitors. Results of the ECR testing demonstrated that coating debondment and corrosion of ECR is directly related to the amount of damage present in the coating, as well as coating thickness. For the bare steel tested with and without corrosion inhibitors, the results showed that corrosion increases with increasing chloride concentrations. Corrosion inhibition characteristics were demonstrated only by the calcium nitrite corrosion inhibitor. A corrosion protection evaluation test was developed for concrete corrosion inhibitor admixtures. The test solution is a simulated concrete pore water. Corrosion is accelerated by evaluating the temperature to field conditions of 40 C. The test consists of a 7 day pretreatment period followed by a 90 day test period. The corrosive sodium chloride is added to the solution containing the bare or epoxy-coated reinforcing steel specimens after the 7 day pretreatment period. In addition, the solution is periodically saturated with oxygen.<br>Master of Science

This investigation is an examination of the behavior of dual coated reinforcing steel (DCR) with defects in the polymer coating exposing the only zinc layer in simulated concrete pore solution with and without chlorides. The intentional defects simulated the condition typically experienced by the rebar in service. Specimens were tested at open circuit potential, +100 mV, -500 mV, and -1000 mV for 30 to 100 days. The results were compared with that from previous DCR investigation with to-steel defects and epoxy-coated rebar (ECR). DCR with to-zinc defects had extensive corrosion damage when under strong anodic polarization and exposed to chlorides and was similar to that seen for DCR with to steel defects. The freely corroding (OCP) to-zinc DCR specimens in solutions both with and with no-chlorides experienced initially very active dissolution which ended after ~1 day. The zinc exposed at the coating breaks was not completely consumed even after 100 days and there was no visible corrosion product accumulation. This may be due to the formation of a calcium hydroxyzincate passive film and shows that the zinc passivates in alkaline solutions without the benefit of a crevice environment. The DCR with to-steel defects and the DCR with to-zinc defects had similar amounts of disbondment for all test conditions. Notable disbondment was seen only in highly anodic polarization regime with chlorides and was due to large amounts of solid corrosion product formation. These results suggest then that the overall process of zinc wastage in DCR in concrete pore water is not likely to be rapid, which would be beneficial to extending the period in which the barrier and galvanic properties of the zinc are maintained.

Corrosion of reinforcing steel in concrete exposed to chloride-laden environments is a well-known and documented phenomenon. The need for cost effective systems for protection against corrosion has become increasingly clear since the first observations of severe corrosion damage to interstate bridges in the 1960's. As one potential solution to the mounting problem of corrosion deterioration of structures, corrosion-inhibiting admixtures have been researched and introduced into service. This report conveys the results of a three-part laboratory study of corrosion inhibiting admixtures in concrete. The commercial corrosion inhibiting admixtures for concrete have been analyzed by three evaluation methods, including: * Conventional concrete corrosion cell prisms under ponding, * Black steel reinforcing bars immersed in simulated concrete pore solutions, * Electrochemical screening tests of special carbon steel specimens in electrochemical corrosion cells containing filtered cement slurry solution. The purposes of the study include: * Determining the influence of a series of commercially available corrosion inhibiting admixtures on general concrete handling, performance and durability properties not related to corrosion. * Determining the effectiveness of corrosion inhibiting admixtures for reduction or prevention of corrosion of reinforcing steel in concrete, relative to untreated systems, under laboratory conditions. * Conducting a short-term pore solution immersion test for inhibitor performance and relating the results to those of the more conventional long-term corrosion monitoring techniques that employ admixtures in reinforced concrete prisms. * Determining whether instantaneous electrochemical techniques can be applied in screening potential inhibitor admixtures. Concrete properties under test included air content, slump, heat of hydration, compressive strength, and electrical indication of chloride permeability. Monitoring of concrete prism specimens included macro-cell corrosion current, mixed-cell corrosion activity as indicated by linear polarization, and ancillary temperature, relative humidity, and chloride concentration documentation. Simulated pore solution specimens were analyzed on the basis of weight loss and surface area corroded as a function of chloride exposure. Electrochemical screening involved polarization resistance of steel in solution. Results include corrosion potential, polarization resistance and corrosion current density.<br>Master of Science

Submitted by Luciana Ferreira (lucgeral@gmail.com) on 2016-10-03T11:31:01Z No. of bitstreams: 2 Dissertação - Plínio Ferreira Pires - 2016.pdf: 6131513 bytes, checksum: 8fa6643740293050fba973c250df0e54 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)<br>Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2016-10-03T11:31:21Z (GMT) No. of bitstreams: 2 Dissertação - Plínio Ferreira Pires - 2016.pdf: 6131513 bytes, checksum: 8fa6643740293050fba973c250df0e54 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)<br>Made available in DSpace on 2016-10-03T11:31:21Z (GMT). No. of bitstreams: 2 Dissertação - Plínio Ferreira Pires - 2016.pdf: 6131513 bytes, checksum: 8fa6643740293050fba973c250df0e54 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2016-07-27<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>The carbonation phenomenon consists in a physicochemical process which reduces the alkalinity of concrete. Carbonation can destabilize the protective layer of the steel, leaving it susceptible to corrosion, which is one of the most significant and costly causes of deterioration in reinforced concrete. Accordingly, chemical analysis of the pore solution has been held for about 60 years, but few studies are focused on types of concrete containing mineral additions subjected to carbonation, due to the difficulty of obtaining the pore solution, given its structure densification under these conditions. Depending on the concrete composition, the natural carbonation process can take several years to present sufficient analyzable data, therefore, most of the studies on this topic use accelerated tests to simulate this phenomenon. However, even with full control of the laboratory environment, it is not possible to reproduce the randomness of the variables responsible for the degradation that occur in real situations. This study aims to evaluate the process of natural carbonation in 36 different types of concrete or analysis conditions, which cover a wide range of characteristics and properties of concrete that represent the various service situations of the structures, after about 14 years of exposure, in typical urban environment. The results are presented for types of concrete with and without mineral additions (silica fume, rice husk ash, metakaolin, fly ash and blast furnace slag); three water/binder (0.40, 0.55 and 0.70) and two curing conditions (dry-cured and moist-cured). The study was conducted by the application of simplified models of carbonation and statistical analysis on an extensive experimental database (over 2000 measurements) obtained by eight evaluations of carbonation carried at different ages, through 14 years of natural exposure prototypes of concrete beams. In addition, chemical analysis of pH, ionic strength and conductivity of the pore solution - obtained through innovative method - were conducted in both the carbonated layer and the non-carbonated layer of concrete. The results indicate that the empirically-analytical model proposed by Tuutti, has an excellent representativity of carbonated depth over time. The use of a coefficient of carbonation, from Tuutti’s model, calculated from early ages, can generate mistaken conclusions: underestimating the dry-cured concrete and overestimating the moist-cured concrete. In the overall analysis of the natural carbonation coefficients obtained by ANOVA showed that the water/binder ratio is the most significant factor, followed by curing type and, finally, the type of addition. The best performances as the carbonation are observed to the lower water/binder concretes, subjected to wet cure. Under the method used to obtain the pore solution, it was possible to compare the difference between the chemical properties of non-carbonated and carbonated layers of each type of concrete analyzed.<br>O fenômeno da carbonatação consiste em um processo físico-químico que leva à redução de alcalinidade do concreto. Isto pode desestabilizar a camada protetora do aço, deixando-o passível de corrosão, que é uma das mais importantes e onerosas causas de deterioração do concreto armado. Nesse sentido, a análise química da solução do poro tem sido realizada há cerca de 60 anos, contudo raros trabalhos focam em concretos submetidos à carbonatação contendo adições minerais, dada a dificuldade de se obter a solução devido à densificação na estrutura porosa nessas condições. Dependendo da composição do concreto, o processo de carbonatação natural pode levar vários anos para apresentar dados passíveis de análise, diante disso, a maioria dos estudos nesse tema utilizam ensaios acelerados para simular tal fenômeno, contudo, mesmo com todo controle do ambiente de laboratório, não se pode reproduzir a aleatoriedade das variáveis que ocorre em situações reais de degradação. Este trabalho tem como objetivo avaliar o processo de carbonatação natural em 36 diferentes concretos ou condições de análise, os quais cobrem uma ampla faixa de características e propriedades dos concretos, representando as mais diversas situações de serviço para as estruturas, após cerca de 14 anos de exposição, em ambiente típico urbano. São, portanto, apresentados resultados de concretos sem e com adições minerais (sílica ativa, cinza de casca de arroz, metacaulim, cinza volante e escória de alto-forno); três relações água/ligante (0,40; 0,55 e 0,70) e duas condições de cura (seca e úmida). O estudo se deu por meio de aplicações de modelos simplificados de carbonatação e análises estatísticas em um extenso banco de dados experimentais (mais de 2000 medidas) obtido por oito avaliações da frente de carbonatação realizadas em diferentes idades, durante 14 anos de exposição natural de protótipos de vigas de concreto. Foram realizadas também análises químicas de pH, força iônica e condutividade da solução do poro, obtida através de método inovador, tanto da camada carbonatada quanto da camada não carbonatada dos concretos. Os resultados indicam que o modelo empírico-analítico, proposto por Tuutti, possui excelente representatividade da profundidade carbonatada ao longo do tempo. A utilização de um coeficiente de carbonatação, do modelo de Tuutti, calculado a partir de idades iniciais pode gerar conclusões equivocadas: subestimando os concretos sem cura e superestimando os de cura úmida. A análise global dos coeficientes de carbonatação, obtidos pela ANOVA, demonstrou que a relação água/ligante é o fator mais significativo, seguido do tipo de cura e, por último, o tipo de adição. Os melhores desempenhos quanto à carbonatação são observados para os concretos de menor relação água/ligante, submetidos à cura úmida. De acordo com o método empregado para obtenção da solução do poro, foi possível comparar a diferença entre as propriedades químicas da camada não carbonatada e a carbonatada, para toda a família de concretos analisada.

Fly ash has been used extensively to control deleterious alkali-silica reaction in concrete. The majority of fly ashes can be used to control ASR induced expansion. Fly ashes with high CaO contents are less effective at reducing expansion and fly ashes with high alkali contents can be counter active. Class C fly ashes are less effective at reducing the pH of the pore solution because they are less pozzolanic. The pozzolanic reaction in Class F fly ashes enhances the ability for the hydration products to bind alkalis. This prevents the availability of these alkalis for ASR. This project aims to characterize fly ash in a way that best predicts how it will perform in concrete with an emphasis on ASR. Fly ashes with a variety of chemical compositions were evaluated using a range of analytical and characterization techniques. Research data from several universities were used to correlate their long term data with this project’s accelerated tests. This research aimed at evaluating the mineralogical, chemical, and physical characteristics that most affect the ability of a given fly ash to prevent ASR-induced expansion and cracking.<br>text