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Advances in Hydration Chemistry for Low-Carbon Cementitious Materials

A Special Issue of Materials (ISSN 1996-1944) belonging to the section "Construction and Building Materials".

Deadline for manuscript submissions: 20 May 2027 | Viewed by 2839

Editors

School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001, China
Interests: cement hydration chemistry; mineral activation; low-carbon cementitious materials; low-calcium clinker; solid waste resource utilization

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Guest Editor
School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001, China
Interests: functionalized green building materials; high performance concrete; low-carbon cementitious materials; solid waste resource utilization

Special Issue Information

Dear Colleagues,

Against the backdrop of global carbon neutrality goals, the cement and concrete industry—one of the largest industrial carbon emitters—has prioritized the development of low-carbon cementitious materials as a core strategy for decarbonization. Innovations such as high-volume supplementary cementitious materials (SCMs, e.g., fly ash, slag, limestone powder), alkali-activated materials (AAMs), low-carbon cement clinkers and bio-based cementitious systems have emerged as mainstream alternatives to traditional Portland cement. However, the macro-performance, microstructure, carbon reduction efficiency and long-term service reliability of these low-carbon cementitious materials are fundamentally governed by their hydration chemistry—including the type, formation rate, and spatial distribution of hydration products, the degree of hydration and interfacial chemical reactions.

Despite significant progress in low-carbon cementitious material research, critical knowledge gaps remain in the field of hydration chemistry: (i) the synergistic hydration mechanisms of multi-component low-carbon systems are still not fully elucidated, especially under complex environmental conditions; (ii) the correlation between micro-scale hydration processes and macro-scale material properties lacks systematic characterization; (iii) efficient chemical regulation strategies for hydration are insufficiently developed; and (iv) the long-term hydration stability of low-carbon cementitious materials and its impact on carbon emission persistence have not been thoroughly explored. These gaps hinder the translation of fundamental research on low-carbon cementitious materials into practical engineering applications.

This Special Issue, “Advances in Hydration Chemistry for Low-Carbon Cementitious Materials”, aims to bridge this divide by focusing on the latest scientific advancements, innovative technologies and engineering practices that link hydration chemistry to the development and optimization of low-carbon cementitious materials. We seek to provide a platform for researchers and engineers worldwide to share cutting-edge findings on the mechanisms, characterization, regulation and application of hydration chemistry in low-carbon systems, thereby advancing the fundamental understanding and industrial implementation of low-carbon cementitious materials. Both original research articles and comprehensive review articles are welcome.

Topics of particular interest encompass, but are not confined to:

  • Hydration reaction mechanisms of multi-component low-carbon cementitious systems;
  • In situ and dynamic characterization techniques for hydration chemistry;
  • Chemical regulation of hydration processes in low-carbon cementitious materials;
  • Correlation between hydration products/microstructure and macro-performance of low-carbon cementitious materials;
  • Hydration behavior of low-carbon cementitious materials under extreme environmental conditions;
  • Life-cycle assessment (LCA) of low-carbon cementitious materials from the perspective of hydration chemistry;
  • Hydration activation mechanisms of industrial solid wastes as alternative cementitious materials;
  • Hydration control strategies for low-carbon cementitious materials in emerging applications;
  • Long-term hydration stability and durability evolution of low-carbon cementitious materials in service;
  • Machine learning and data-driven modeling of hydration chemistry for low-carbon cementitious materials design and performance prediction.

This Special Issue aligns with the journal’s mission to promote sustainable innovation in civil engineering materials and support global decarbonization efforts. We look forward to receiving your valuable contributions that will advance the science of hydration chemistry and accelerate the adoption of low-carbon cementitious materials in the construction industry.

Dr. Lei Liu
Dr. Xiaohai Liu
Guest Editors

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Keywords

  • low-carbon cementitious materials
  • hydration chemistry
  • microstructure
  • characterization techniques
  • chemical regulation
  • life-cycle assessment
  • long-term hydration stability
  • machine learning

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Published Papers (3 papers)

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Research

28 pages, 34091 KB  
Article
Effects of Titanium Gypsum and Flue Gas Desulfurization Gypsum on the Hydration and Mechanical Properties of Anhydrite–Phosphogypsum-Based Supersulfated Cement
by Youquan Xie, Li Yang, Xiaodong Li, Jiaqing Wang, Yanbo Li, Hao Zhou and Yueyang Hu
Materials 2026, 19(6), 1273; https://doi.org/10.3390/ma19061273 - 23 Mar 2026
Cited by 1 | Viewed by 833
Abstract
Supersulfated cement (SSC) is an environmentally friendly cementitious material with a low clinker content, in which industrial byproduct gypsum serves as the sulfate source, thereby enabling the valorization of solid waste. The hydration process, pore structure, microstructure, and hydration products were investigated using [...] Read more.
Supersulfated cement (SSC) is an environmentally friendly cementitious material with a low clinker content, in which industrial byproduct gypsum serves as the sulfate source, thereby enabling the valorization of solid waste. The hydration process, pore structure, microstructure, and hydration products were investigated using paste samples by means of isothermal calorimetry, X-ray diffraction (XRD), thermogravimetric analysis (TG–DTG), Fourier transform–infrared spectroscopy (FT-IR), mercury intrusion porosimetry (MIP), and scanning electron microscopy (SEM), while compressive strength was evaluated using mortar specimens. Compared with ordinary Portland cement (OPC), SSC offers clear advantages in reducing energy consumption and greenhouse gas emissions. In this study, the effects of titanium gypsum (TG) and flue gas desulfurization gypsum (FGD) on the hydration behavior, fluidity, mechanical properties, and microstructural evolution of an anhydrite (AH)–phosphogypsum (PG)-based SSC were systematically investigated. The results indicate that the incorporation of 11% TG and FGD mitigates the strong sulfate environment caused by the rapid dissolution of soluble AH, thereby regulating the hydration process. As the proportion of TG and FGD increased, the cumulative heat release within 72 h gradually decreased. When AH was completely replaced, the cumulative heat release of TG4 and FG4 decreased by approximately 19.7% and 28.6%, respectively. TG and FGD exhibited opposite effects on the fluidity of SSC while both promoting strength development. Among all mixtures, TG2 and FG2 showed the best performance, with the highest 28-day compressive strengths of 50.15 MPa and 51.95 MPa, respectively. Microstructural analysis reveals that differences in particle size distribution and dissolution kinetics among gypsums governed the sulfate release characteristics and slag activation mechanisms, thus leading to distinct hydration pathways, pore structure evolution, and microstructural densification. This study provides a theoretical basis for the efficient utilization of various industrial byproduct gypsums and offers important guidance for the controllable design of SSC performance. Full article
(This article belongs to the Special Issue Advances in Hydration Chemistry for Low-Carbon Cementitious Materials)
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21 pages, 8221 KB  
Article
Study on the Regulation of Diethylene Glycol on the Hydration Process of High-Activity Calcium Oxide
by Yu Fan, Wei Guo, Yueyang Hu, Yue Zhang, Jiaqing Wang and Zhaijun Wen
Materials 2026, 19(6), 1132; https://doi.org/10.3390/ma19061132 - 14 Mar 2026
Cited by 1 | Viewed by 759
Abstract
Traditional calcium hydroxide (Ca(OH)2) typically exhibits low specific surface area and reactivity, significantly limiting its efficacy in industrial gas–solid reactions such as flue gas desulfurization and thermochemical energy storage. To address these limitations, this study proposes a two-stage synthesis strategy designed [...] Read more.
Traditional calcium hydroxide (Ca(OH)2) typically exhibits low specific surface area and reactivity, significantly limiting its efficacy in industrial gas–solid reactions such as flue gas desulfurization and thermochemical energy storage. To address these limitations, this study proposes a two-stage synthesis strategy designed to enhance the surface properties and chemical activity of Ca(OH)2. The process involves the preparation of high-activity calcium oxide (CaO), followed by controlled hydration using diethylene glycol (DEG). Drawing on established mechanisms from cement chemistry, wherein potassium ions (K+) catalyze the decomposition of calcium carbonate (CaCO3), limestone particles (10–20 mm) were pre-soaked in a 0.1 mol/L potassium nitrate (KNO3) solution for 48 h prior to calcination. Characterization via X-ray diffraction (XRD), scanning electron microscopy (SEM), and Blaine Air Permeability Method analysis revealed that this pretreatment accelerated decomposition kinetics by inducing surface defects, yielding CaO with a maximum reactivity of 435.7 mL. Subsequent hydration at 80 °C with 70 wt% DEG effectively suppressed particle agglomeration and promoted the formation of thin platelet structures. The resulting Ca(OH)2 achieved a utilization efficiency of 98.5% and a specific surface area of 43.24 m2/g, demonstrating a robust technical route for fabricating high-performance calcium-based sorbents for environmental and energy applications. Full article
(This article belongs to the Special Issue Advances in Hydration Chemistry for Low-Carbon Cementitious Materials)
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21 pages, 4949 KB  
Article
Corrosion Resistance of Fly Ash-Enhanced Cement-Based Materials in High-Chloride Gas Storage Reservoirs
by Hong Fu, Defei Chen, Bao Zhang, Hongjun Wu, Sheng Huang, Weizhi Tuo, Kun Chen, Hexiang Zhou and Yuanwu Dong
Materials 2026, 19(2), 406; https://doi.org/10.3390/ma19020406 - 20 Jan 2026
Cited by 2 | Viewed by 737
Abstract
This study investigates the use of fly ash to mitigate the long-term performance degradation of Portland cement-based sealing materials in high-salinity environments, such as those found in gas storage reservoirs. We systematically evaluated the evolution of material properties under different temperatures and curing [...] Read more.
This study investigates the use of fly ash to mitigate the long-term performance degradation of Portland cement-based sealing materials in high-salinity environments, such as those found in gas storage reservoirs. We systematically evaluated the evolution of material properties under different temperatures and curing periods. Our integrated methodology combining mechanical tests, microstructural analysis, and chloride migration assessment, reveals a multi-faceted mechanism by which fly ash enhances chloride resistance. The key findings demonstrate that reactive Al2O3 in fly ash promotes the formation of Friedel’s salt, increasing chemical chloride binding and reducing the chloride ingress rate in the Portland cement–Fly ash system (PFS) to only 26.6% of that in the Portland Cement system (PCS). Concurrently, the pozzolanic reaction consumes portlandite (Ca(OH)2), forming stable C-A-S-H gel and refining the pore structure by filling interconnected channels. This nanoscale pore refinement decreased permeability by nearly an order of magnitude. After 90 days of curing in 90 °C saline solution, PFS achieved a compressive strength of 28.2 MPa and maintained an exceptionally low internal chloride content of 0.08 wt.%, demonstrating superior long-term durability. This work clarifies the synergistic mechanisms of fly ash modification and temperature effects, providing a theoretical basis for optimizing sealing materials for deep geological reservoirs and experimental support for the application of fly ash in high-temperature, high-salinity engineering environments. Full article
(This article belongs to the Special Issue Advances in Hydration Chemistry for Low-Carbon Cementitious Materials)
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