Yannick H. Emminger, Luca Ladner, Cristina Ruiz-Agudo
{"title":"Comparative study of the early stages of crystallization of calcium silicate hydrate (C-S-H) and calcium aluminate silicate hydrate (C-A-S-H)","authors":"Yannick H. Emminger, Luca Ladner, Cristina Ruiz-Agudo","doi":"10.1016/j.cemconres.2025.107873","DOIUrl":"10.1016/j.cemconres.2025.107873","url":null,"abstract":"<div><div>The use of SCMs as partial substitutes for PC has made C-A-S-H a key binding phase in modern cement, yet its crystallization mechanism remains elusive. This study investigates the early stages of synthetic C-A-S-H formation and compares them with C-S-H using double addition of stoichiometric calcium and silicon amounts at a Ca/Al ratio of 5. Through real-time monitoring of solution parameters—transmittance, free Ca<sup>2+</sup> conductivity, and pH—complemented by structural and morphological characterization (FTIR, XRD, SEM, TEM, and NMR), we demonstrate that C-A-S-H formation is at least a two-step process involving amorphous globules, which then evolve into foil-like particles with higher crystallinity. Additionally, we reveal that Al promotes Ca binding during the prenucleation stage and slightly accelerates nucleation. These results highlight important differences in the formation pathways of both hydrates, particularly the extended stability of the C-A-S-H globules, which might affect the workability and setting time in aluminium-containing blended cements.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"193 ","pages":"Article 107873"},"PeriodicalIF":10.9,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143608516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Corrosion behavior of steel reinforcement in magnesium silicate hydrate (M-S-H) concrete","authors":"Dan Meng, En-Hua Yang, Shunzhi Qian","doi":"10.1016/j.cemconres.2025.107858","DOIUrl":"10.1016/j.cemconres.2025.107858","url":null,"abstract":"<div><div>Magnesium silicate hydrate (M-S-H) binder has been considered a promising alternative binder for engineering application. However, its low pH environment raises concerns for its adoption in steel reinforced concrete structures. To evaluate the corrosion behavior of steel reinforced M-S-H system under ambient and chloride environments, electrochemical tests were conducted. Additionally, phase formation, microstructure development, pore structure and solution chemistry were evaluated to better understand the corrosion mechanism. Corrosion resistance of the tested M-S-H system subjected to ambient environment was higher than that of the PC system because of significantly higher impedance of the bulk matrix, which was attributed to lower internal moisture, finer pore structure and lower conductivity of the pore solution in the M-S-H system. When subjected to cyclic chloride immersion, the M-S-H system exhibited higher corrosion rate, which was mainly due to its low pH and more electrolyte available on the steel surface.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"193 ","pages":"Article 107858"},"PeriodicalIF":10.9,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143598871","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zhanzhao Li , Christopher A. Gorski , Aaron Thompson , Jeffrey R. Shallenberger , Gopakumar Kaladharan , Aleksandra Radlińska
{"title":"Dissolution kinetics of iron sulfide minerals in alkaline solutions","authors":"Zhanzhao Li , Christopher A. Gorski , Aaron Thompson , Jeffrey R. Shallenberger , Gopakumar Kaladharan , Aleksandra Radlińska","doi":"10.1016/j.cemconres.2025.107850","DOIUrl":"10.1016/j.cemconres.2025.107850","url":null,"abstract":"<div><div>Deleterious aggregate reactions induced by iron sulfide minerals, especially pyrrhotite and pyrite, have devastated concrete structures across many global regions. While these minerals have been extensively studied under acidic conditions, their behavior in alkaline environments, such as concrete, remains poorly understood. This study investigates the kinetics and mechanisms of iron sulfide dissolution at high pH (13–14). Results revealed that pyrrhotite dissolves orders of magnitude more rapidly than pyrite, with dissolution rates increasing with both pH and temperature. The type of alkali (potassium or sodium) in the solution was not found to affect the dissolution behavior. Kinetic modeling and experimental characterization indicated that the dissolution kinetics of pyrrhotite is controlled by a combination of chemical reactions (oxidation of iron and sulfur species) and diffusion (through an Fe(III)-(oxy)hydroxide layer). These findings provide practical insights into controlling dissolution and mitigating iron sulfide-induced damage in concrete.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"193 ","pages":"Article 107850"},"PeriodicalIF":10.9,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143590120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Rate effect on the pull-out load of individual fibers in concrete: A probabilistic modeling approach","authors":"Takeru Kanazawa , John E. Bolander","doi":"10.1016/j.cemconres.2025.107857","DOIUrl":"10.1016/j.cemconres.2025.107857","url":null,"abstract":"<div><div>Understanding of the load-rate dependence of fiber pull-out from concrete has been hindered by the large scatter of test data. Relatively little attention has been given to the statistical nature of single-fiber pull-out under different loading rates. The present study is based on a probabilistic interpretation of the pull-out phenomenon, assessing the statistical fluctuations observed in the common finding that complete pull-out occurs at greater load levels under higher loading rates. Since progressive debonding along the fiber–matrix interface affects the pull-out behavior, interfacial crack growth is modeled using a fracture mechanics approach. Based on a theoretical justification, the transition probability to debonding is devised and implemented within a Markov chain model. The Markov model accounts for debonding propagation with each stress increment until complete pull-out. The results demonstrate that the probability distributions of stress at complete pull-out differ from a normal distribution. The coefficient of variation is also independent of the loading rates. These findings show reasonable agreement with statistical variations observed from test data.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"193 ","pages":"Article 107857"},"PeriodicalIF":10.9,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143590118","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
R. Besselink , A. Poulain , M. la Bella , A.-L. Auzende , S. Goberna-Ferron , M.P. Asta , V. Magnin , S. Bureau , L. Fernández-Carrasco , A.E.S. Van Driessche , A. Fernandez-Martinez
{"title":"High energy X-ray scattering reveals the short-range order of proto-C-S-H: Implications for the nucleation of cement hydrates","authors":"R. Besselink , A. Poulain , M. la Bella , A.-L. Auzende , S. Goberna-Ferron , M.P. Asta , V. Magnin , S. Bureau , L. Fernández-Carrasco , A.E.S. Van Driessche , A. Fernandez-Martinez","doi":"10.1016/j.cemconres.2025.107855","DOIUrl":"10.1016/j.cemconres.2025.107855","url":null,"abstract":"<div><div>The heterogeneous nature of the cement clinker, its complex coupled dissolution/re-precipitation process and the complex defect chemistry of the hydrates formed during cement hydration, make that the nucleation and growth mechanisms of cement hydrates are not fully understood. Recent studies have suggested the existence of a disordered precursor prior to the crystallization of C-S-H. Here, a combination of X-ray scattering and electron microscopy experiments are used to study the structure and crystallization kinetics of this amorphous intermediate. Our results suggest that proto-C-S-H is predominantly composed of 6-fold oxygen-to-calcium coordinated CaO<sub>x</sub> polyhedra, in contrast to the 7-fold coordinated polyhedra in C-S-H with a tobermorite-like structure. The addition of gluconate, a widely used additive, resulted in an increased kinetic persistence of proto-C-S-H. Overall, our study provides new insights into the formation and structure of proto-C-S-H, and suggests that it plays an important role in the crystallization mechanism of C-S-H.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"193 ","pages":"Article 107855"},"PeriodicalIF":10.9,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143590050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yikai Liu , Maria Chiara Dalconi , Maurizio Pietro Bellotto , Luca Valentini , Simone Molinari , Xinyi Yuan , Daolin Wang , Wei Hu , Qiusong Chen , Alejandro Fernandez-Martinez , Gilberto Artioli
{"title":"Pb-induced retardation of early hydration of Portland cement: Insights from in-situ XRD and implications for substitution with industrial by-products","authors":"Yikai Liu , Maria Chiara Dalconi , Maurizio Pietro Bellotto , Luca Valentini , Simone Molinari , Xinyi Yuan , Daolin Wang , Wei Hu , Qiusong Chen , Alejandro Fernandez-Martinez , Gilberto Artioli","doi":"10.1016/j.cemconres.2025.107867","DOIUrl":"10.1016/j.cemconres.2025.107867","url":null,"abstract":"<div><div>Using industrial by-products as substitutes for Ordinary Portland Cement (OPC) is a promising strategy to reduce its environmental impact. However, heavy metals like Pb strongly interfere with initial kinetics. The dynamic physicochemical environment makes it challenging to identify the key factors. Here, we employed <em>in-situ</em> XRD as a time-dependent method, alongside conventional characterization techniques and geochemical modeling, to investigate the Pb-induced retardation in CEMI 42.5R and 52.5R. The results show that Pb-hydroxides and Pb-O-Si clusters are expected to be the primary mechanisms for this inhibition. Among clinker phases, C<sub>3</sub>A dissolution is less affected and serves as the primary source of alkalinity in early hydration, promoting hydration products precipitation and gypsum dissolution. Geochemical modeling suggests that Pb species concentration in the solution regulates the precipitation of hydration products, especially portlandite. The comparison of hydration kinetics of 2 types of OPC highlights optimizing particle size as a solution to mitigate retardation impact.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"193 ","pages":"Article 107867"},"PeriodicalIF":10.9,"publicationDate":"2025-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143576380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A preliminary study on an effective and simplistic self-healing concept for cement using coarse clinker particles as the healing agent","authors":"Jialiang Wang, Min Wu","doi":"10.1016/j.cemconres.2025.107859","DOIUrl":"10.1016/j.cemconres.2025.107859","url":null,"abstract":"<div><div>Effective, low-cost and simplistic self-healing strategies for cement-based systems are attractive. This work proposed a concept where coarse clinker particles were used to replace cement and acted as the healing agent, and the effectiveness was validated by comprehensive studies. The results showed the high potential of the clinker sizes (40–60 μm, 60–90 μm, 0.5–1 mm) and replacement ratios (20–40%) under the studied conditions. For the clinker sized 40–60 μm, the 28d tensile and compressive strength recovery rates achieved 1.12 and 0.91, and the 56d crack sealing width and area reached 300–400 μm and 83.4%–94.4%, which even exceeds conventional autonomous self-healing strategies. The microscopic analyses indicated that larger clinker particles affected reaction kinetics of hydrating particles and improved spatial distribution of the hydration products. By retaining abundant unhdyrated parts and leading to more uniform distribution of the hydration products, the coarse clinker particles significantly improved self-healing properties of the cement mixes.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"193 ","pages":"Article 107859"},"PeriodicalIF":10.9,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143546521","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"From bauxite residue mineralogy to reactivity and properties of blended cements","authors":"Michael Wenzel, Fabien Georget, Thomas Matschei","doi":"10.1016/j.cemconres.2025.107854","DOIUrl":"10.1016/j.cemconres.2025.107854","url":null,"abstract":"<div><div>This paper reviews the efforts taken towards developing bauxite residue (BR) based blended cements (>30% substitution) contributing to the cement industry's net-zero targets, while utilizing the Bayer-processes by-product. We provide a comprehensive review of physical properties, element composition and mineralogy of Bayer and sintering BR. This defines the main challenges that BR based SCMs have to overcome to be utilized in sustainable blended cements. Several activation treatments and their impact on SCM characteristics and reactivity are introduced and compared to other reactive SCMs.</div><div>Furthermore, the review summarizes the impact of BR addition on the engineering performance of blended cements and includes selected durability issues. Our main goal is linking macroscopic observations to microstructural features of the binders and outlining a way towards a complete understanding of these blended cements. We outline specific knowledge gaps, in particular the effect of bauxite residues on the phase assemblage and microstructure of blended cements.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"192 ","pages":"Article 107854"},"PeriodicalIF":10.9,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143532580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Mechanisms governing in-depth infiltration of crack filling solutions in concrete using a magnetic approach","authors":"Onur Ozturk, Sriramya Duddukuri Nair","doi":"10.1016/j.cemconres.2025.107856","DOIUrl":"10.1016/j.cemconres.2025.107856","url":null,"abstract":"<div><div>Cracks reduce the strength and service life of concrete structures. Although high-performance crack filling materials are available in market, achieving deep infiltration is often difficult. In this work, we propose the utilization of a magnetic approach for enhanced infiltration and examine the mechanisms governing its effectiveness. Our experiments demonstrate that employing magnetic fields in the milliTesla range can significantly enhance the filling ability of solutions containing <1% by volume of magnetic particles. To facilitate flow observations and gain a deeper understanding of the fundamental mechanisms, we used transparent box samples and guar gum solutions in this study. In line with the objectives of this study, we discuss potential mechanisms relevant to real concrete cracks and crack filling materials. Finally, we provide suggestions for field implementation of the proposed technology, considering the typical characteristics of concrete cracks and structural elements.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"192 ","pages":"Article 107856"},"PeriodicalIF":10.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143526500","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Songyue Chai , Jianyu Song , Muhan Wang , Yue Zhang , Bo-Tao Huang , Bing Yin , Pan Wang , Dongshuai Hou
{"title":"Freezing behavior of ionic solutions within calcium silicate hydrate gel pores","authors":"Songyue Chai , Jianyu Song , Muhan Wang , Yue Zhang , Bo-Tao Huang , Bing Yin , Pan Wang , Dongshuai Hou","doi":"10.1016/j.cemconres.2025.107841","DOIUrl":"10.1016/j.cemconres.2025.107841","url":null,"abstract":"<div><div>Salt-frost damage is a crucial issue affecting the durability of concrete structures, however, the freezing behavior and micro-mechanisms of ionic solutions within cementitious material gel pores remain unclear, which is not conducive to optimizing cold-resistant concrete design from the bottom up. In this study, the models of saturated calcium silicate hydrate (C-S-H) gel pores containing NaCl, Na<sub>2</sub>SO<sub>4</sub>, and aqueous solution, respectively, were constructed by molecular dynamics (MD) simulation. We investigated the freezing behavior of ionic solutions within the gel pores at 230 K. The freezing process of models exhibited a distinct periodic pattern. Na<sup>+</sup> and Cl<sup>−</sup> delayed the freezing of pore water, while <span><math><msubsup><mi>SO</mi><mn>4</mn><mrow><mn>2</mn><mo>−</mo></mrow></msubsup></math></span> accumulated near the freezing front, significantly hindering freezing progression. The freezing resulted in two types of nano brine pockets in the NaCl model. This work provides new molecular insights into salt freezing in cementitious materials and informs the design of cold-resistant concrete at the molecular scale.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"192 ","pages":"Article 107841"},"PeriodicalIF":10.9,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143518892","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}