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19 pages, 6569 KiB  
Article
Sustainable Cementitious Materials: Strength and Microstructural Characteristics of Calcium Carbide Residue-Activated Ground Granulated Blast Furnace Slag–Fly Ash Composites
by Xing Liu, Guiyuan Xiao, Dunhan Yang, Lin Dai and Aiwei Tang
Sustainability 2024, 16(24), 11168; https://doi.org/10.3390/su162411168 - 19 Dec 2024
Viewed by 665
Abstract
This study developed a sustainable low-carbon cementitious material using calcium carbide residue (CCR) as an alkali activator, combined with ground granulated blast furnace slag (GGBS) and fly ash (FA) to form a composite. The objective was to optimize the CCR dosage and the [...] Read more.
This study developed a sustainable low-carbon cementitious material using calcium carbide residue (CCR) as an alkali activator, combined with ground granulated blast furnace slag (GGBS) and fly ash (FA) to form a composite. The objective was to optimize the CCR dosage and the GGBS-to-FA ratio to enhance the unconfined compressive strength (UCS) of the composite, providing a viable alternative to traditional Portland cement while promoting solid waste recycling. Experiments were conducted with a water-to-binder ratio of 0.55, using six GGBS-to-FA ratios (0:10, 2:8, 4:6, 6:4, 8:2, and 10:0) and CCR contents ranging from 2% to 12%. Results indicated optimal performance at a GGBS-to-FA ratio of 8:2 and an 8% CCR dosage, achieving a peak UCS of 18.04 MPa at 28 days, with 79.88% of this strength reached within just 3 days. pH testing showed that with 8% CCR, pH gradually decreased over the curing period but increased with higher GGBS content, indicating enhanced reactivity. Microstructural analyses (XRD and SEM-EDS) confirmed the formation of hydration products like C-(A)-S-H, significantly improving density and strength. This study shows CCR’s potential as an effective and environmentally friendly activator, advancing low-carbon building materials and resource recycling in construction. Full article
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<p>Particle size grading curves of CCR, GGBS, and FA.</p>
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<p>XRD spectrum of GGBS.</p>
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<p>XRD spectrum of FA.</p>
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<p>XRD spectrum of CCR.</p>
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<p>The whole process of the test.</p>
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<p>UCS of specimens with different GGBS/FA ratios at different CCR doping levels. (<b>a</b>) CCR = 2, 4, and 6%; (<b>b</b>) CCR = 8, 10, and 12%.</p>
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<p>Specimens with 8% CCR, with a GGBS/FA ratio of 10:0.</p>
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<p>The effect of CCR dosage on the UCS of G8F2.</p>
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<p>Effect of maintenance time on UCS of composite cementitious materials.</p>
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<p>Effect of FA-GGBS ratio and curing time on pH value.</p>
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<p>Microscopic test results of G0F10: (<b>a</b>) morphology, (<b>b</b>) energy spectrum of region A; and (<b>c</b>) XRD.</p>
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<p>Microscopic test results of G4F6: (<b>a</b>) SEM morphology, (<b>b</b>) energy spectrum of region B, and (<b>c</b>) XRD.</p>
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<p>Microscopic test results of G8F2: (<b>a</b>) SEM morphology, (<b>b</b>) energy spectrum of region C, and (<b>c</b>) XRD.</p>
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<p>Microscopic test results of G10F0: (<b>a</b>) SEM morphology, (<b>b</b>) energy spectrum of region D, and (<b>c</b>) XRD.</p>
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<p>Chemical reaction process of CCR to stimulate GGBS-FA cementitious material.</p>
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23 pages, 491 KiB  
Article
Definition and Identification of Honey Bee Welfare Practices Within the Five Domains Framework for Sustainable Beekeeping
by Giovanni Formato, Elena Giannottu, Valentina Lorenzi, Cristina Roncoroni, Marco Pietropaoli, Camilla Pedrelli, Marina Bagni and Stefano Palomba
Appl. Sci. 2024, 14(24), 11902; https://doi.org/10.3390/app142411902 - 19 Dec 2024
Viewed by 286
Abstract
This paper aims to define and identify the Honey Bee Welfare Practices (HBWPs) that beekeepers should adopt within a modern framework for sustainable apiculture. Once identified, HBWPs were categorized according to the Five Domains Model used in other animal species. Drawing on findings [...] Read more.
This paper aims to define and identify the Honey Bee Welfare Practices (HBWPs) that beekeepers should adopt within a modern framework for sustainable apiculture. Once identified, HBWPs were categorized according to the Five Domains Model used in other animal species. Drawing on findings of the European BPRACTICES Horizon 2020 project, we identified, for the first time, 243 HBWPs: while all practices were considered impacting the mental state domain, 38 were assigned to nutrition/hydration, 90 to environment, 220 to health, and 50 to behavior. The proposed HBWPs aim to fill existing gaps by introducing a new approach that more fully respects honey bee behavior and helps prevent unnecessary suffering for each bee and the whole beehive at the same time. Future efforts should focus on maximizing welfare benefits within the One Welfare framework, moving beyond the previously considered One Health perspective. This welfare-oriented focus benefits honey bees, supports beekeepers, and promotes environmental sustainability, aligning with the principles of One Welfare. Full article
(This article belongs to the Special Issue New Advances in Beekeeping, Bee Behavior and Its Bionic Applications)
13 pages, 5248 KiB  
Article
Improving the Effect of Calcined Salt Mud on Mechanical Properties of 3D Printing Materials Using Recycled Construction Aggregates
by Yuntao Wang, Shangjin Jiang, Sudong Hua, Hongfei Yue and Yanan Zhang
Appl. Sci. 2024, 14(24), 11868; https://doi.org/10.3390/app142411868 - 19 Dec 2024
Viewed by 286
Abstract
Using solid waste-based materials, such as recycled building aggregate (RCA), preparing 3D-printed materials can reduce costs but increase the water–cement ratio of the printed material, which reduces its mechanical performance. In order to solve the problem of mechanical properties decline caused by an [...] Read more.
Using solid waste-based materials, such as recycled building aggregate (RCA), preparing 3D-printed materials can reduce costs but increase the water–cement ratio of the printed material, which reduces its mechanical performance. In order to solve the problem of mechanical properties decline caused by an increase in the w/c ratio, this experiment found that adding calcined salt mud (CSM) to the printing materials and changing the water-to-cement ratio from 0.37 to 0.4 CSM can ensure that the compressive strength of the printing materials remains basically unchanged. Moreover, through TG, SEM, and other microscopic data, it can be seen that calcium hydroxide in CSM can not only participate in the synergistic reaction of ethylene/vinyl acetate copolymer (EVA) and dust ash (DA), produce more NaOH, and promote the hydration of granulated blast furnace slag (GBFS) but also promote the formation of ettringite together with SO42− in solution, optimizing pore size distribution. Full article
(This article belongs to the Section Additive Manufacturing Technologies)
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<p>Salt mud analyses.</p>
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<p>Particle size of raw material.</p>
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<p>Static yield stress.</p>
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<p>Printing viscosity.</p>
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<p>Mechanical strengths of different w/c ratios.</p>
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<p>Hydration heat analysis of different samples. (<b>a</b>) The incremental curves og heat flow vs. hydration (A1: heat of hydration water of C3S. A2: hydrolysis of C3A, the formation of sulphoaluminate, and the hydration exotherm of GBFS. A3: the formation of AFM between residual C3A and ettringite). (<b>b</b>) The cumulative exothermic curve.</p>
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<p>TG and DSC analysis of mixture at 28d.</p>
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<p>Results of rheological tests on the prepared mixtures.</p>
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<p>Scanning electron microscopy (SEM) image of the sample.</p>
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20 pages, 8144 KiB  
Article
Failure Behavior of Nano-Metakaolin Concrete Under Splitting Tension Based on Digital Image Correlation Method
by Hao Chen, Yingfang Fan, Qiuchao Li and Chang Peng
Polymers 2024, 16(24), 3482; https://doi.org/10.3390/polym16243482 - 13 Dec 2024
Viewed by 416
Abstract
Nano metakaolin (NMK) has attracted considerable interest for its potential to improve the durability of cementitious materials. However, the effect of NMK on the splitting tensile performance of concrete has not been systematically investigated. This study investigates the splitting tensile performance of NMK [...] Read more.
Nano metakaolin (NMK) has attracted considerable interest for its potential to improve the durability of cementitious materials. However, the effect of NMK on the splitting tensile performance of concrete has not been systematically investigated. This study investigates the splitting tensile performance of NMK concrete and analyzes its failure behavior under splitting load. Different NMK dosages (0%, 1%, 3%, 5%, and 7%) were considered, and splitting tensile tests were conducted. The crack propagation process, crack width, and crack growth rate on the surface of NMK concrete during the splitting tensile test are analyzed using the Digital Image Correlation (DIC) method. The mechanisms by which NMK affects the splitting tensile performance of concrete were examined using X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscopy/Energy Dispersive Spectroscopy (SEM/EDS), and Thermogravimetric Analysis (TG). The results indicate that the incorporation of NMK enhances the splitting tensile performance of concrete. Concrete with 5% NMK addition exhibited the highest splitting tensile strength, with an increase of 17.4% compared to ordinary concrete. NMK improved the cracking resistance and overall integrity under splitting tensile load. With 5% NMK addition, the surface crack length, width, and main crack propagation rate of the concrete decreased by 4.5%, 35.3%, and 29.6%, respectively. NMK contributed to a denser internal structure of the concrete, promoted the formation of C-S-H gel, and increased the degree of cement hydration. Moreover, a lower thickness and Ca/Si ratio of interfacial transition zone (ITZ) were observed in NMK concrete. The ITZ thickness and Ca/Si ratio of concrete with 5% NMK were reduced by 64.4% and 85.4%, respectively, compared to ordinary concrete. In summary, the influence mechanism of NMK addition on the splitting tensile strength and failure behavior of concrete is explored in this study, providing experimental data to support the application of NMK concrete in practical engineering. Full article
(This article belongs to the Special Issue Polymer Admixture-Modified Cement-Based Materials)
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<p>The physical index of materials. (<b>a</b>) XRD pattern; (<b>b</b>) TEM morphology; (<b>c</b>) particle size distribution.</p>
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<p>Preparation of NMK concrete.</p>
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<p>The setup of the compressive and splitting tensile strength tests.</p>
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<p>The test devices and the required samples.</p>
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<p>The splitting tensile strength of NMK concrete.</p>
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<p>Splitting tensile load-displacement curves of NMK concrete.</p>
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<p>The strain clouds of NMK concrete surface at different loading stages.</p>
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<p>The process of initiation, propagation, and penetration of main crack.</p>
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<p>Failure crack pattern of NMK concrete.</p>
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<p>The fractal dimension of NMK concrete.</p>
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<p>Relationship between fractal dimension of failure cracks and splitting tensile strength.</p>
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<p>XRD patterns of NMK concrete.</p>
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<p>FTIR curves of NMK concrete.</p>
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<p>SEM images of NMK concrete.</p>
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<p>Schematic diagram of EDS line scan position.</p>
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<p>Distribution Patterns of Ca and Si in NM0.</p>
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<p>Distribution Characteristics of Ca and Si in NMK Concrete.</p>
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<p>Distribution Characteristics of Ca and Si in NMK Concrete.</p>
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<p>TG-DTG curves of concrete with NMK content.</p>
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21 pages, 9724 KiB  
Article
Study on pH-Responsive Delayed, Cross-Linking and Weighted Fracturing Fluid
by Hao Bai, Fujian Zhou, Xinlei Liu, Xiaozhi Xin, Huimin Zhao, Zhiyuan Ding, Yunjin Wang, Xin Wang, Xingting Li, Wei Li and Erdong Yao
Molecules 2024, 29(24), 5847; https://doi.org/10.3390/molecules29245847 - 11 Dec 2024
Viewed by 362
Abstract
Hydraulic fracturing of deep, high-temperature reservoirs poses challenges due to elevated temperatures and high fracture pressures. Conventional polymer fracturing fluid (QCL) has high viscosity upon adding cross-linking agents and significantly increases wellbore friction. This paper examines a polymer fracturing fluid with pH response [...] Read more.
Hydraulic fracturing of deep, high-temperature reservoirs poses challenges due to elevated temperatures and high fracture pressures. Conventional polymer fracturing fluid (QCL) has high viscosity upon adding cross-linking agents and significantly increases wellbore friction. This paper examines a polymer fracturing fluid with pH response and low friction. Experimental results indicate that cross-linking occurs quickly in acid, while alkali can slow the cross-linking process and reduce friction. Sodium carbonate (Na2CO3) serves as an effective candidate. An optimized formulation consisting of “salt + pH + polymer + cross-linking agent” is proposed in two stages: low viscosity for fracture generation and high viscosity for sand transport. PH control enhances polymer hydration, increasing sand-carrying in the low-viscosity stage. Scanning electron microscopy (SEM) reveals that the fluid’s structure varies with pH, showing that alkali promotes a stable network structure. Infrared spectroscopy (IR) shows that higher pH increases negative charges of the polymer chains, which enhances their hydrodynamic radius, slightly raises viscosity, and enhances sand carrying. Field tests confirm the formulation’s effectiveness, leading to lower operating pressures, stable sand transport, and notable production, averaging 107.57 m3 of oil and 276 m3 of gas per day. Overall, this research provides low-friction solutions for the efficient development of deep reservoirs. Full article
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<p>Laboratory temperature and shear resistance of the QCL cross-linking and weighted fracturing fluid system (pH = 6–7).</p>
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<p>Laboratory gel breaking and dissolution test of the QCL cross-linking and weighted fracturing fluid system: (<b>a</b>) the residue content changes with the gel-breaking time; (<b>b</b>) gel-breaking situation of the QCL fluid system; (<b>c</b>) the dissolution situation of the QCL fluid system.</p>
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<p>Cross-linking situations of the QCL fracturing fluid system under different pH conditions: (<b>a</b>) hanging time and viscosity of the QCL fluid under different pH conditions; (<b>b</b>) hanging state of the QCL fluid.</p>
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<p>The temperature and shear resistance situations of the QCL fracturing fluid system under different pH conditions: (<b>a</b>) pH = 3; (<b>b</b>) pH = 9; (<b>c</b>) pH = 12.</p>
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<p>Temperature and shear resistance situations of NaOH-adjusted QCL fracturing fluid system.</p>
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<p>Temperature and shear resistance situations of NaHCO<sub>3</sub>-adjusted QCL fracturing fluid system.</p>
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<p>The gel breaking of the QCL fracturing fluid system under different alkali types (from left to right: NaHCO<sub>3</sub>, NaOH, and Na<sub>2</sub>CO<sub>3</sub>).</p>
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<p>Viscosity changes of the QCL fracturing fluid system with only pH adjustment cross-linking.</p>
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<p>Temperature and shear resistance situations of the QCL fracturing fluid system with only pH adjustment cross-linking.</p>
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<p>Viscoelastic modulus curves of cross-linking fracturing fluid under different conditions: (<b>a</b>) Only pH—low viscosity stage; (<b>b</b>) Only cross-linked agent—low viscosity stage; (<b>c</b>) pH + cross-linking agent—high viscosity stage.</p>
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<p>Temperature and shear resistance situations of the QCL fracturing fluid system under different conditions (from left to right: only pH, only cross-linking agent, pH + cross-linking agent).</p>
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<p>The friction reduction rate curves of cross-linking fracturing fluid under different conditions.</p>
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<p>SEM structure of the QCL polymer fracturing fluid under different conditions: (<b>a</b>) only pH- acid conditions (400 μm accuracy); (<b>b</b>) only cross-linking agent (100 μm accuracy); (<b>c</b>) only pH- alkali conditions (100 μm accuracy); (<b>d</b>) pH + cross-linking agent (100 μm accuracy).</p>
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<p>Infrared spectra of the QCL fracturing fluid system under different pH conditions.</p>
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<p>Acid-promoted organic zirconium cross-linking agent releases zirconium ions.</p>
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<p>Charge and hydrolysis changes of the QCL polymer in the process of gradually adding sodium carbonate.</p>
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<p>Field fracturing operation curve of Man X well.</p>
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<p>Field fracturing curves of Man X well after adjusting pump sequence.</p>
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<p>Production situations after fracturing in Man X well.</p>
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20 pages, 9896 KiB  
Article
Enhancing Mid-Term Strength and Microstructure of Fly Ash–Cement Paste Backfill with Silica Fume for Continuous Mining and Backfilling Operations
by Xiaoping Shao, Zhengchun Wang, Renlong Tang, Bingchao Zhao, Jianbo Ning, Chuang Tian, Wei Wang, Yibo Zhang and Xing Du
Materials 2024, 17(24), 6037; https://doi.org/10.3390/ma17246037 - 10 Dec 2024
Viewed by 474
Abstract
Fly ash–cement composite backfill slurry, prepared by partially replacing cement with fly ash, has been demonstrated to effectively reduce the mine backfill costs and carbon emissions associated with cement production. However, the use of fly ash often results in insufficient early and medium-term [...] Read more.
Fly ash–cement composite backfill slurry, prepared by partially replacing cement with fly ash, has been demonstrated to effectively reduce the mine backfill costs and carbon emissions associated with cement production. However, the use of fly ash often results in insufficient early and medium-term strength of the backfill material. To address the demand for high medium-term strength in backfill materials under continuous mining and backfilling conditions, this study developed a silica fume–fly ash–cement composite backfill slurry. The effects of varying silica fume contents on the slurry’s flowability, uniaxial compressive strength, microstructure, and pore characteristics were systematically investigated. The results showed that increasing the silica fume content significantly reduced the slurry’s flowability. However, at a silica fume content of 5%, the slurry achieved optimal medium-term strength, with a 14-day uniaxial compressive strength of 3.98 MPa, representing a 25% improvement compared to the control group. A microstructural analysis revealed that a moderate silica fume content promoted the formation of calcium silicate hydrate gel, filled micropores, and optimized the pore structure, thereby enhancing the overall strength and durability of the material. Conversely, an excessive silica fume content above 5% led to a marked decrease in both flowability and strength. Based on a comprehensive evaluation of silica fume’s effects on the flowability, strength, and microstructure, the optimal silica fume content was determined to be 5%. This study provides a theoretical basis and practical guidance for improving the efficiency of continuous mining and backfilling operations, and for designing high-performance backfill materials suitable for continuous mining and filling conditions. Full article
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<p>Particle size distribution of SF.</p>
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<p>XRD results for fly ash.</p>
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<p>Experimental flow chart.</p>
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<p>The initial and final condensation times of SFCP.</p>
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<p>Slump and diffusivity of fresh SFCP slurry.</p>
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<p>Shear stress of SFCP slurry.</p>
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<p>Apparent viscosity of SFCP slurry.</p>
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<p>UCS of SFCP at four ages.</p>
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<p>XRD results for SFCP samples at 14 days.</p>
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<p>SEM images of SFCP at 14 days of age. (<b>a</b>) C-SF0. (<b>b</b>) C-SF2.5. (<b>c</b>) C-SF5. (<b>d</b>) C-SF7.5. (<b>e</b>) C-SF10.</p>
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<p>Pore size distribution curve of SFCP.</p>
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25 pages, 5862 KiB  
Article
The Effect of μ-Limestone Additions on the Mechano-Chemical and Microstructural Properties of Slag and Binary Slag/Ground Fly Ash Alkaline-Activated Binders
by Francisco Javier Vázquez-Rodríguez, Lucio Guillermo López-Yépez, Nora Elizondo-Villarreal, Ana María Guzmán-Hernández, Lauren Yolanda Gómez-Zamorano and Edén Amaral Rodríguez-Castellanos
Materials 2024, 17(23), 5940; https://doi.org/10.3390/ma17235940 - 4 Dec 2024
Viewed by 538
Abstract
An alternative approach to reducing the clinker factor, i.e., worldwide CO2 emissions resulting from the production of composite cement, is to replace these materials with supplementary aluminosilicate-based materials that promote the formation of alkali-activated cements, whose elevated temperature resistance, limited permeability, strong [...] Read more.
An alternative approach to reducing the clinker factor, i.e., worldwide CO2 emissions resulting from the production of composite cement, is to replace these materials with supplementary aluminosilicate-based materials that promote the formation of alkali-activated cements, whose elevated temperature resistance, limited permeability, strong binding properties, excellent durability, high chemical corrosion resistance, confinement of toxic waste, and environmentally low impact have attracted a lot of attention in the cement industry. The principal aluminosilicate-based supplementary materials (SCMs) used in the cement industry are fly ash and blast-furnace slag. Recently, limestone has been proposed for use in alkali-activated cement to improve mechanical resistance and promote nucleation sources for the hydration of hybrid gels. In the current research work, the effect of 5 and 10 wt% limestone additions to slag and fly ash/slag alkali-activated cements with NaOH-4M was studied to evaluate the mechano-chemical and microstructural properties of alkali-activated cement. The effect of limestone was studied using mechanical resistance, XRD, FTIR, SEM-EDS, and calorimetry methods. The XRD, FTIR, and SEM-EDS results demonstrated the formation of portlandite Ca(OH)2 after the activator solution’s reaction with limestone. The limestone’s dissolution in Ca2+ contributes to hybrid gel formation ((N, C)-A-S-H, N-A-S-H, and C-A-S-H), resulting in compressive strength higher than 20 MPa, the recommended resistance for commercial cement. Full article
(This article belongs to the Section Construction and Building Materials)
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<p>(<b>a</b>) Diffractograms of raw materials (limestone—LSP, ground fly ash—MFA, and slag—S). C, M, Q, and W refer to limestone, mullite, quartz, and merwinite, respectively. (<b>b</b>) Particle size distribution of raw materials (limestone—LSP, ground fly ash—MFA, and slag—S).</p>
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<p>(<b>a</b>) X-ray diffraction and (<b>b</b>) FTIR analyses of treatment of limestone powders in different solutions. CaCO<sub>3</sub> (713, 881, 1435, 1812, 2515, 2875, and 2982 cm<sup>−1</sup>). Ca(OH)<sub>2</sub> (1031 and 3640 cm<sup>−1</sup>).</p>
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<p>The microstructure of (<b>a</b>) μ-limestone submerged in water and (<b>b</b>) μ-limestone submerged in NaOH for 28 days and the variation in chemical composition in terms of the mineralogical nature of the limestone investigated by EDS microanalysis.</p>
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<p>Compressive strength results.</p>
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<p>Flexural strength results.</p>
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<p>Microstructure of the 100S10C paste. (<b>a</b>) Distribution of the limestone embedded in the cementitious matrix and (<b>b</b>) interaction of limestone with the slag paste.</p>
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<p>Microstructure of the 60S40MFA10C paste. (<b>a</b>) shows the interaction of limestone with hybrid hydration gels. (<b>b</b>) shows the dissolution of the particles and the formation of hydration gels such as the N-A-S-H gel and hybrid (N, C)-A-S-H gel formation.</p>
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<p>Microstructure of the 60S40MFA10C paste. (<b>a</b>) shows the formation of a well-defined portlandite-Ca(OH)<sub>2</sub> with hexagon-like morphology. (<b>b</b>) shows the formation of (N, C)-A-S-H and N-A-S-H gels.</p>
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<p>Mineralogical formation of compounds in the 100S paste with and without the addition of limestone. (<b>a</b>) 100S paste, (<b>b</b>) 100S5C paste, and (<b>c</b>) 100S10C paste. Calcite (Cc), quartz (q), mullite (M), merwinite (W), tobermorite (C), and hydrotalcite (H).</p>
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<p>Mineralogical formation of compounds in the 60S40MFA paste with and without the addition of limestone. (<b>a</b>) 60S40MFA paste, (<b>b</b>) 60S40MFA5C paste, and (<b>c</b>) 60S40MFA10C paste. Calcite (Cc), quartz (q), mullite (M), merwinite (W), tobermorite (C), and hydrotalcite (H).</p>
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<p>(<b>a</b>) FTIR spectra of 100S paste and (<b>b</b>) 100S510C paste.</p>
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<p>(<b>a</b>) FTIR spectra of 60S40MFA paste and (<b>b</b>) 60S40MFA10C paste.</p>
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<p>Heat flow of mixtures: (<b>a</b>) 0.5 h and (<b>b</b>) time scale of 2 h.</p>
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<p>Heat flow of all mixtures with limestone additions. (<b>a</b>) Time scale of 100 h and (<b>b</b>) 25 h.</p>
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18 pages, 6388 KiB  
Article
Deep Learning-Assisted Analysis of GO-Reinforcing Effects on the Interfacial Transition Zone of CWRB
by Jiajian Yu, Zhiwei Chen, Xiaoli Xu, Xinjie Su, Shuai Liang, Yanchao Wang, Junqing Hong and Shaofeng Zhang
Materials 2024, 17(23), 5926; https://doi.org/10.3390/ma17235926 - 4 Dec 2024
Viewed by 479
Abstract
Understanding the enhancing mechanisms of graphene oxide (GO) on the pore structure characteristics in the interfacial transition zone (ITZ) plays a crucial role in cemented waste rock backfill (CWRB) nanoreinforcement. In the present work, an innovative method based on metal intrusion techniques, backscattered [...] Read more.
Understanding the enhancing mechanisms of graphene oxide (GO) on the pore structure characteristics in the interfacial transition zone (ITZ) plays a crucial role in cemented waste rock backfill (CWRB) nanoreinforcement. In the present work, an innovative method based on metal intrusion techniques, backscattered electron (BSE) images, and deep learning is proposed to analyze the micro/nanoscale characteristics of microstructures in the GO-enhanced ITZ. The results showed that the addition of GO reduced the interpore connectivity and the porosity at different pore throats by 53.5–53.8%. GO promotes hydration reaction in the ITZ region; reduces pore circularity, solidity, and aspect ratio; enhances the mechanical strength of CWRB; and reduces transport performance to form a dense microstructure in the ITZ. Deep learning-based analyses were then proposed to classify and recognize BSE image features, with a high average recognition accuracy of 95.8%. After that, the deep Taylor decomposition (DTD) algorithm successfully located the enhanced features of graphene oxide modification in the ITZ. The calculation and verification of the typical pore optimization area of the location show that the optimization efficiency reaches 9.6–9.8%. This study not only demonstrated the deepening of the enhancement effect of GO on the pore structure in cement composites and provided new insights for the structural modification application of GO but also revealed the application prospect of GO in the strengthening of CWRB composites and solid waste recycling. Full article
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<p>(<b>a</b>) ITZ aperture color map of CWRB sample; (<b>b</b>) ITZ equivalent aperture distribution of CWRB samples under different w/c ratios. Mechanical properties of the Ref group and GO-modified CWRB specimens: (<b>c</b>) tensile strength and (<b>d</b>) Young’s modulus.</p>
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<p>(<b>a</b>) The color distribution changes in the ITZ aperture when the pore throat threshold is set to 1.03 µm, 1.54 µm, and 2.05 µm. The relationship between cumulative porosity and equivalent pore size of the ITZ under different pore throats of (<b>b</b>) 1.03 µm, (<b>c</b>) 1.54 µm, and (<b>d</b>) 2.05 µm. The measured equivalent aperture distributions of the ITZ under different pore throats are (<b>e</b>) 1.03 µm, (<b>f</b>) 1.54 µm, and (<b>g</b>) 2.05 µm.</p>
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<p>(<b>a</b>) Circularity, (<b>b</b>) solidity, and (<b>c</b>) aspect ratio of the ITZ pore structure in the CWRB sample.</p>
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<p>CNN architecture design.</p>
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<p>The calculated confusion matrix shows (<b>a</b>) the image recognition accuracy at different w/c when the image size is 160 pixels; (<b>b</b>) the image recognition accuracy at the same w/c; (<b>c</b>) the recognition accuracy of four groups of CWRB samples by a CNN algorithm under different training image sizes; and (<b>d</b>) typical examples of image representation precision maps trained at 130, 160, and 190 pixels.</p>
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<p>Extraction and visualization of the CWRB sample enhanced feature pattern based on deep learning. (<b>a</b>) The Ref group and (<b>e</b>) the GO group correctly classified typical BSE images by deep learning. (<b>b</b>) DTD visual heat maps of the Ref group and (<b>f</b>) the GO group, representing microscale characteristic patterns of BSE images. The correlation between each pixel in the BSE image and the classification decision is represented by a color bar. (<b>c</b>) The Ref group and (<b>g</b>) the GO group locations of feature regions in training images. Feature regions of (<b>d</b>) the Ref group and (<b>h</b>) the GO group in CWRB samples extracted from training images.</p>
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<p>(<b>a</b>) Pore color distribution changes in ITZ typical characteristic regions when the pore throat threshold is set to 0.51 µm and 1.03 µm. The relationship between cumulative porosity and equivalent pore size of ITZ under different pore throats is (<b>b</b>) 0.51 µm and (<b>d</b>) 1.03 µm. The measured equivalent pore size distributions of the ITZ under different pore throats are (<b>c</b>) 0.51 µm and (<b>e</b>) 1.03 µm.</p>
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15 pages, 2266 KiB  
Article
Optimizing Cement Content in Controlled Low-Strength Soils: Effects of Water Content and Hydration Time
by Yilian Luo, Liangwei Jiang, Libing Qin, Qiang Luo, David P. Connolly and Tengfei Wang
Materials 2024, 17(23), 5915; https://doi.org/10.3390/ma17235915 - 3 Dec 2024
Viewed by 482
Abstract
The Ethylene Diamine Tetra-acetic Acid (EDTA) titration test is widely used for determining cement content, but its reliability is influenced by the hydration process of cement, which is affected by factors such as water content and hydration time. Despite their importance, these factors [...] Read more.
The Ethylene Diamine Tetra-acetic Acid (EDTA) titration test is widely used for determining cement content, but its reliability is influenced by the hydration process of cement, which is affected by factors such as water content and hydration time. Despite their importance, these factors have received limited attention in existing research. This study explores the relationships between the volume of titrant required for stabilization, cement content, water content, and hydration time. Using a regression orthogonal test, the primary and secondary relationships, as well as the interdependencies among these factors, are analyzed. Results reveal a negative linear relationship between the titrant volume and both water content and hydration time. Cement content, water content, and hydration time are identified as the most significant factors, with minimal interdependencies observed. Within the test parameters, calculated values exhibit an error margin below 2.4%. Deviations of 2.9% in water content and 86 min in hydration time correspond to an approximate 0.5% change in cement content. These findings offer valuable insights for optimizing cement content detection in Controlled Low-Strength Material (CLSM) mixes, promoting more sustainable construction practices. Full article
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<p>EDTA titration test: (<b>a</b>) Procedure; (<b>b</b>) Reagent preparation; (<b>c</b>) Phenomena observed during testing.</p>
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<p>Orthogonal experimental design.</p>
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<p>Relationship between volume of titrant used (<span class="html-italic">V</span>) and cement content (<span class="html-italic">C</span>).</p>
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<p>Relationship between volume of titrant used (<span class="html-italic">V</span>) and water content (<span class="html-italic">W</span>).</p>
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<p>Relationship between volume of titrant used (<span class="html-italic">V</span>) and hydration time (<span class="html-italic">T</span>).</p>
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<p>Variation in cement content detection error (Δ<span class="html-italic">c</span>) with changes in water content (Δ<span class="html-italic">w</span>) and hydration time (Δ<span class="html-italic">t</span>).</p>
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20 pages, 21889 KiB  
Article
The Effects of Combined Use of Sodium Citrate and PCE Plasticizer on Microstructure and Properties of Binary OPC-CAC Binder
by Victoria Shvetsova, Vadim Soloviev, Evgenii Matiushin and Vladimir Erofeev
Materials 2024, 17(23), 5901; https://doi.org/10.3390/ma17235901 - 2 Dec 2024
Viewed by 459
Abstract
This study examines the impact of sodium citrate and a plasticizing additive, along with their sequential introduction into a cement slurry or concrete mix, on the heat evolution of the cement slurry, the microstructure, phase composition of the cement paste, and the compressive [...] Read more.
This study examines the impact of sodium citrate and a plasticizing additive, along with their sequential introduction into a cement slurry or concrete mix, on the heat evolution of the cement slurry, the microstructure, phase composition of the cement paste, and the compressive strength of fine-grained concrete. The binder used in this research was a blended binder consisting of 90% Portland cement and 10% calcium aluminate cement. This type of binder is characterized by an increased heat evolution and accelerated setting time. The addition of sodium citrate at 5% of the binder mass alters the phase composition of newly formed compounds by increasing the quantity of AFt and AFm phases. The presence of sodium citrate significantly delays the hydration process of tricalcium silicate by a factor of 3.3. Initially, it accelerates belite hydration by 31.6%, but subsequently slows it down, with a retardation of 43.4% observed at 28 days. During the hardening process, the hydration of tricalcium aluminate and tetracalcium aluminoferrite is accelerated throughout the hardening process, with the maximum acceleration occurring within the first 24 h. During the first 24 h of hydration, the dissolution rates of tricalcium aluminate and tetracalcium aluminoferrite were 40.7% and 75% faster, respectively. Sodium citrate enhances heat evolution during the initial 24 h by up to 4.3 times and reduces the induction period by up to 5 times. Furthermore, sodium citrate promotes early strength development during the initial curing period, enhancing compressive strength by up to 6.4 times compared to the reference composition. Full article
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<p>XRD pattern of Portland cement.</p>
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<p>XRD pattern of calcium aluminate cement.</p>
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<p>Mixer Controls.</p>
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<p>Microscope FEI Quanta 250.</p>
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<p>Isothermal calorimeter TAM Air.</p>
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<p>Diffractometer ARL X’TRA.</p>
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<p>Testing machine Controls.</p>
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<p>Dependence of heat flow on time: (<b>a</b>) 4 h; (<b>b</b>) 12 h; (<b>c</b>) 168 h.</p>
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<p>Cumulative heat evolution.</p>
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<p>Mass fractions of phases of the composition: (<b>a</b>) 10/90; (<b>b</b>) 10/90+SC 5%.</p>
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<p>Dependence of concrete strength on the addition sequence of additives: (<b>a</b>) compressive strength of concrete samples at 3 days, (<b>b</b>) compressive strength of concrete samples at 28 days.</p>
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16 pages, 3139 KiB  
Article
Properties of Cement-Based Materials Incorporating Ground-Recycled Diatom
by Carlos Rodriguez, Fernando Fernandez, Roberto Rodriguez, Marina Sanchez, Pablo Gómez, Felipe Martí, Miriam Hernández, Isabel Miñano, Carlos Parra, Francisco Benito and Irene Beleña
Crystals 2024, 14(12), 1030; https://doi.org/10.3390/cryst14121030 - 28 Nov 2024
Viewed by 503
Abstract
This research investigates the use of recycled diatomaceous earth (diatomite) from the wine, beer, and oil industries as supplementary cementitious materials in cement-based mixtures. This study aims to reduce embodied energy and promote circular economy practices by incorporating these industrial by-products. The research [...] Read more.
This research investigates the use of recycled diatomaceous earth (diatomite) from the wine, beer, and oil industries as supplementary cementitious materials in cement-based mixtures. This study aims to reduce embodied energy and promote circular economy practices by incorporating these industrial by-products. The research evaluates the compressive strength, durability, and pozzolanic activity of the mixtures over 7, 28, and 90 days of hydration. The results demonstrate that uncalcined diatoms from wine and oil showed lower compressive strength than natural diatomite, whereas calcination at 500 °C significantly improved performance. Beer diatoms exhibited the lowest mechanical strength because of the organic matter content in their composition. The incorporation of quicklime failed to induce pozzolanic activity in uncalcined diatoms; however, calcination at 500 °C led to improved long-term performance, highlighting the importance of heat treatment for activating diatoms’ pozzolanic properties. This study concludes that recycled diatoms, particularly when calcined, have potential as sustainable cementitious materials. Full article
(This article belongs to the Section Hybrid and Composite Crystalline Materials)
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<p>Concrete pipes made with diatomite cement [<a href="#B33-crystals-14-01030" class="html-bibr">33</a>].</p>
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<p>Natural diatoms (N) and recycled diatoms from the filtering of beer (B), wine (W), and oil (O). Beer diatoms (B) appear together with some mill balls in the picture.</p>
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<p>Particle size distribution of natural diatomite (N) and recycled diatoms (B, W, and O).</p>
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<p>TGA of diatoms (N, B, W, and O).</p>
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<p>Evolution of Water demand replacing OPK by Natural (N) and Beer (B) diatoms (wt%).</p>
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<p>Evolution of Water demand replacing OPK by Wine (W) and Oil (O) diatoms (wt%).</p>
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<p>Setting time of different formulations according to the origin of the diatom.</p>
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<p>Setting time of different formulations according to the origin of the diatom.</p>
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16 pages, 4704 KiB  
Article
Promoting Sustainability in the Cement Industry: Evaluating the Potential of Portuguese Calcined Clays as Clinker Substitutes for Sustainable Cement Production
by Karyne Ferreira dos Santos, Samuel Santos, Manuel Vieira, António Santos Silva and Cinthia Maia Pederneiras
Sustainability 2024, 16(23), 10365; https://doi.org/10.3390/su162310365 - 27 Nov 2024
Viewed by 789
Abstract
The cement industry significantly contributes to global CO2 emissions, posing several challenges for a future low-carbon economy. In order to achieve the target established by the European Sustainable Development Goals of reaching carbon neutrality by 2050, the European Cement Association (Cembureau) has [...] Read more.
The cement industry significantly contributes to global CO2 emissions, posing several challenges for a future low-carbon economy. In order to achieve the target established by the European Sustainable Development Goals of reaching carbon neutrality by 2050, the European Cement Association (Cembureau) has devised a comprehensive roadmap based on five key approaches, referred to as the 5C strategies. Portland clinker is one of the crucial concerns, since its production emits over 60% of the cement manufacturing emissions. Therefore, supplementary cementitious materials (SCMs) to partially replace clinker content in cement have gained significant attention in providing alternatives to traditional clinker in cement production. This paper evaluates the potential of Portuguese calcined clays (CCs) as viable substitutes for clinker to enhance sustainability in cement manufacturing. More than 50 clays were characterised through chemical and mineralogical analyses to assess their reactivity and suitability for calcination using the strength activity index (SAI), along with XRD, XRF, and TGA techniques. This study investigated the calcination conditions that provide the best clay reactivity, which were subsequently used for calcination. This investigation is part of a project to evaluate the behaviour of calcined clays through mechanical, hydration, and durability properties. The findings indicate that Portuguese calcined clays exhibit promising pozzolanic activity. Furthermore, these clays could significantly reduce CO2 emissions and raw material consumption in cement production. This research underscores the potential of local calcined clays as a sustainable clinker substitute, promoting eco-friendly practices in the construction industry. Full article
(This article belongs to the Special Issue CO2 Capture and Utilization: Sustainable Environment)
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<p>Clays collected in Portugal.</p>
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<p>CaO-SiO<sub>2</sub>-Al<sub>2</sub>O<sub>3</sub> phase diagram (Clays are represented as grey dots).</p>
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<p>Gaussian distribution for the principal reactive minerals: (<b>a</b>) kaolinite, (<b>b</b>) illite, and (<b>c</b>) montmorillonite.</p>
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<p>Gaussian distribution for (<b>a</b>) quartz and (<b>b</b>) muscovite.</p>
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<p>Mineral compositions of the different clay samples.</p>
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<p>DTG curves of reference clays and samples under analysis.</p>
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<p>Graphic showing the regions of clay reactivity.</p>
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<p>Gaussian distribution for (<b>a</b>) humidity results and (<b>b</b>) LOI results.</p>
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<p>Compressive strength of the hardened cement mortars for the selected calcined clays (700 °C, 800 °C, and 900 °C) and reference cement.</p>
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<p>Strength activity index (SAI) for clay samples (800 °C).</p>
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29 pages, 12142 KiB  
Review
Research Progress and Outlook of Molecular Dynamics Simulation on Carbon Dioxide Applied for Methane Exploitation from Hydrates
by Qiannan Yu, Chenglong Li, Boyang Peng, Huimin Tang, Tao Yang, Yang Yu, Kun Zhang and Zhijing Chen
Molecules 2024, 29(23), 5579; https://doi.org/10.3390/molecules29235579 - 26 Nov 2024
Viewed by 506
Abstract
Research progress of carbon dioxide applied for methane exploitation from hydrates is summarized, with a focus on advances in molecular dynamics simulations and their application in understanding the mechanism of carbon dioxide replacement for hydrate exploitation. The potential of carbon dioxide in enhancing [...] Read more.
Research progress of carbon dioxide applied for methane exploitation from hydrates is summarized, with a focus on advances in molecular dynamics simulations and their application in understanding the mechanism of carbon dioxide replacement for hydrate exploitation. The potential of carbon dioxide in enhancing energy recovery efficiency and promoting carbon capture and storage is emphasized. An overview is provided of the advancements made in utilizing carbon dioxide for methane hydrate exploitation, highlighting its significance. Subsequently, the theoretical foundations and techniques of molecular dynamics simulations are delved into, encompassing key elements such as statistical ensembles, molecular force fields, and numerical solution methods. Through simulations, various characterization parameters including mean square displacement, radial distribution functions, coordination numbers, angular order parameters, and hydrogen bonds are computed and analyzed, which are crucial for understanding the dynamic changes in hydrate structures and the replacement process. Thorough research and analysis have been conducted on the two possible and widely debated mechanisms involved in the replacement of methane hydrates by carbon dioxide, with a particular emphasis on guest molecular replacement and hydrate reconfiguration. These processes encompass the intricate interactions between carbon dioxide molecules and the cage-like structure of hydrates, as well as the rearrangement and stabilization of hydrate structures. Several key issues surrounding the application of carbon dioxide for methane hydrate exploitation are identified, including the influence of thermodynamic conditions, the selection of auxiliary gases, and other potential factors such as geological conditions and fluid properties. Addressing these issues is crucial for optimizing the extraction process and enhancing economic and environmental benefits. A theoretical foundation and technical reference for the application of carbon dioxide in methane hydrate exploitation are provided, while future research directions and priorities are also outlined. Full article
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<p>Equilibrium curves of methane hydrate and carbon dioxide hydrates for different salinities.</p>
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<p>High-frequency keyword clustering co-occurrence map of natural gas hydrates.</p>
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<p>Water molecule angular order parameters for different hydrate layers (Tung, Y.T. et al., 2011 [<a href="#B54-molecules-29-05579" class="html-bibr">54</a>]).</p>
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<p>Variation in the oxygen atom pair distribution function during simulation (Qi, Y. et al., 2011 [<a href="#B56-molecules-29-05579" class="html-bibr">56</a>]).</p>
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<p>Trajectories of carbon dioxide molecules in hydrate cages at 315 K (Liang, S. et al., 2016 [<a href="#B57-molecules-29-05579" class="html-bibr">57</a>]. Where green wireframe represents cage structure of hydrate, combination of one green ball and two blue balls represents carbon dioxide molecule).</p>
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<p>Conformational diagram of the system for the replacement of methane hydrate by carbon dioxide in NaCl solution (Yi, L. et al., 2016 [<a href="#B58-molecules-29-05579" class="html-bibr">58</a>]).</p>
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<p>Coordination number of water molecules in hydrates (Iwai, Y. et al., 2012 [<a href="#B59-molecules-29-05579" class="html-bibr">59</a>]).</p>
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<p>Initial system conformation (Bai, D. et al., 2012 [<a href="#B60-molecules-29-05579" class="html-bibr">60</a>]).</p>
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<p>Hydration numbers in different regions (Bai, D. et al., 2012 [<a href="#B60-molecules-29-05579" class="html-bibr">60</a>]).</p>
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<p>Variation in the number of hydrogen bonds in methane hydrates with simulation time under different temperature conditions (Uddin, M. et al., 2014 [<a href="#B61-molecules-29-05579" class="html-bibr">61</a>]).</p>
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<p>Variation in the number of hydrate cages for pressures of 20 bar and 50 bar at 255 K temperature (Wu, G. et al., 2019 [<a href="#B62-molecules-29-05579" class="html-bibr">62</a>]).</p>
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<p>RDF values for methane hydrate at 2–210 K (Cladek, B.R. et al., 2021 [<a href="#B65-molecules-29-05579" class="html-bibr">65</a>]).</p>
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<p>RDF of particles in the system at 3MPa with different temperatures (Guo, P. et al., 2022 [<a href="#B66-molecules-29-05579" class="html-bibr">66</a>]).</p>
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<p>Changes in the number of methane and carbon dioxide molecules with temperature (Gajanayake, S. et al., 2022 [<a href="#B67-molecules-29-05579" class="html-bibr">67</a>]).</p>
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<p>Variation in tetrahedrality order parameter with temperature at 8 MPa pressure (Gajanayake, S. et al., 2022 [<a href="#B67-molecules-29-05579" class="html-bibr">67</a>]).</p>
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<p>RDF of hydrate oxygen atom pairs (<b>a</b>), methane hydrate (<b>b</b>), and carbon dioxide hydrate (<b>c</b>) at different temperatures (Cheng, L. et al., 2024 [<a href="#B68-molecules-29-05579" class="html-bibr">68</a>]).</p>
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<p>MSD of nitrogen and carbon dioxide in nitrogen hydrate and carbon dioxide hydrate (Liu, J. et al., 2016 [<a href="#B70-molecules-29-05579" class="html-bibr">70</a>]).</p>
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<p>Recovery of methane in the replacement of natural gas hydrates with pure nitrogen, pure carbon dioxide, and nitrogen–carbon dioxide gas mixtures in different ratios (Matsui, H. et al., 2016 [<a href="#B71-molecules-29-05579" class="html-bibr">71</a>]).</p>
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<p>RDF of pure carbon dioxide (<b>a</b>), pure nitrogen (<b>b</b>), and nitrogen–carbon dioxide gas mixtures (<b>c</b>) before and after gas hydrate replacement (Song, W. et al., 2020 [<a href="#B72-molecules-29-05579" class="html-bibr">72</a>]).</p>
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<p>Number of replaced methane molecules varies with time, 265 K (Li, D. et al., 2021 [<a href="#B73-molecules-29-05579" class="html-bibr">73</a>]).</p>
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<p>F4φ order parameters for different system substitutions at 260 K and 50 MPa (Palodkar, A.V. et al., 2022 [<a href="#B74-molecules-29-05579" class="html-bibr">74</a>]).</p>
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<p>RDF of carbon dioxide hydrate with time in pure water and porous media systems (Zhang, X. et al., 2023 [<a href="#B75-molecules-29-05579" class="html-bibr">75</a>]).</p>
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<p>Changes in the number of methane and carbon dioxide molecules with initial carbon dioxide concentration (Gajanayake, S. et al., 2022 [<a href="#B67-molecules-29-05579" class="html-bibr">67</a>]).</p>
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14 pages, 10241 KiB  
Article
An Experimental Investigation of the Hydrate Formation Mechanism in the Throttling of Carbon Dioxide-Containing Trace Moisture
by Zhen Xu, Wenlei Xu, Zeli Dai, Rong Cao, Lina Meng, Zengqi Liu, Yiwei Wang, Qiang Sun, Jianyi Chen and Xuqiang Guo
Processes 2024, 12(12), 2665; https://doi.org/10.3390/pr12122665 - 26 Nov 2024
Viewed by 497
Abstract
Carbon capture, utilization and storage are facilitated through carbon dioxide (CO2) transport. Pipe transportation is the main method for transporting CO2. However, hydrate blockages reduce transport efficiency in the pipelines, and the throttling devices are the main location of [...] Read more.
Carbon capture, utilization and storage are facilitated through carbon dioxide (CO2) transport. Pipe transportation is the main method for transporting CO2. However, hydrate blockages reduce transport efficiency in the pipelines, and the throttling devices are the main location of hydrate blockages. In this paper, the mechanism of hydrate formation in the throttling of CO2-containing trace moisture was investigated. The throttling device in a pipe was mimicked using a cylindrical orifice plate. The work also studied the effects of moisture content, upstream pressure and upstream temperature on hydrate formation. The results indicate that the Joule–Thomson cooling effect is a key contributor, and promotes the condensation of trace moisture, resulting in the free water necessary for hydrate nucleation. Under the effect of gas flow back-mixing, it is easy for the hydrate to adhere to the inner surface of the pipe behind the orifice plate. When the moisture content in the gas increases from 123 μmol/mol to 1024 μmol/mol, the hydrate induction time decreases from infinity to 792 s. However, the moisture content has no effect on the adhesion strength of the hydrate to the inner surface of the pipe. When the initial upstream pressure increases from 2.0 MPa to 3.5 MPa, the hydrate induction time decreases from infinity to 306 s. When the upstream temperature decreases from 291.15 K to 285.15 K, the hydrate induction time decreases from infinity to 330 s. With the decrease in the initial upstream temperature, the adhesion of hydrate particles to the inner surface of the pipe is promoted. This study provides experimental evidence for the characteristics of hydrate formation in the process of CO2 throttling. Full article
(This article belongs to the Section Chemical Processes and Systems)
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<p>The throttling experimental device. 1. Gas cylinder; 2. reduction valve; 3. flash tank; 4. the heating water bath; 5. Pt100 platinum resistance; 6. heat exchange coil; 7. pressure transmitter; 8. front transparent tube; 9. throttle orifice plate; 10. rear transparent tube; 11. SONY DV; 12. air bath; 13. the heating water bath; 14. back pressure valve; 15. dew point meter; 16. rotor flow meter.</p>
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<p>The phenomenon of hydrate formation and deposition in the throttling process. (<b>a</b>) Schematic diagram of orifice plate. (<b>b</b>) Various time-based states of water/hydrate. (<b>c</b>) Downstream pressure (<math display="inline"><semantics> <mrow> <msub> <mrow> <mi>P</mi> </mrow> <mrow> <mi mathvariant="normal">r</mi> </mrow> </msub> </mrow> </semantics></math>) of diagram. (<b>d</b>) Downstream temperature (<math display="inline"><semantics> <mrow> <msub> <mrow> <mi>T</mi> </mrow> <mrow> <mi mathvariant="normal">r</mi> </mrow> </msub> </mrow> </semantics></math>) of diagram.</p>
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<p>Hydrate formation mechanism in throttling of CO<sub>2</sub>-containing trace moisture.</p>
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<p>Throttling characteristics under different moisture contents. (<b>a</b>) The pressure response. (<b>b</b>) The statistical characteristics of pressure response.</p>
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<p>The induction time of hydrate in different moisture content conditions.</p>
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<p>The temperature response of the CO<sub>2</sub> with different moisture content in throttling process.</p>
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<p>Throttling characteristics under different upstream pressures. (<b>a</b>) The pressure response. (<b>b</b>) The statistical characteristics of pressure response.</p>
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<p>The induction time of hydrate in different initial upstream pressure conditions.</p>
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<p>The temperature response with different initial upstream pressures in throttling process.</p>
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<p>Throttling characteristics under different initial upstream temperatures. (<b>a</b>) The pressure response. (<b>b</b>) The statistical characteristics of pressure response.</p>
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<p>The induction time of hydrate in different initial upstream temperature conditions.</p>
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<p>The temperature change in the outlet of throttle orifice at different initial upstream temperatures.</p>
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16 pages, 3480 KiB  
Article
Research on Mechanical Properties of Silica Fume Cementitious Materials Excited by Wet Grinding Methods
by Canhao Zhao, Ben Li, Kaihang Li and Zhuocheng Li
Buildings 2024, 14(12), 3757; https://doi.org/10.3390/buildings14123757 - 25 Nov 2024
Viewed by 381
Abstract
Silica fume (SF) has been widely used in engineering; however, its densification during transportation reduces its original pozzolanic activity. This paper investigates the effects of wet grinding and chemical activation on the mechanical properties and hydration products of silica fume in cement-based materials, [...] Read more.
Silica fume (SF) has been widely used in engineering; however, its densification during transportation reduces its original pozzolanic activity. This paper investigates the effects of wet grinding and chemical activation on the mechanical properties and hydration products of silica fume in cement-based materials, revealing the mechanism by which wet grinding improves these properties. The results indicate that wet grinding effectively reduces the particle size of silica fume. Under optimal excitation conditions (250 r/min, 20 min), the median particle size is reduced to 12.1 μm, 2.27 times smaller than before excitation. The 28-day compressive strength of the silica fume cement paste reaches 60.8 MPa, 23.7% higher than that of the reference group. This approach effectively mitigates nano-agglomeration, enhances the pozzolanic activity of silica fume, and promotes AFt and C-S-H gel formation. The findings demonstrate that wet grinding activation can further enhance the utilization rate of silica fume. Full article
(This article belongs to the Section Building Materials, and Repair & Renovation)
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<p>Cement composition and silica ash composition of graphite tailings.</p>
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<p>Experimental and research flow chart of this paper.</p>
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<p>Particle size distribution of silica fume.</p>
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<p>Compressive strength of cement paste specimen: (<b>a</b>) compressive strength of 150 r/min; (<b>b</b>) compressive strength of 250 r/min; (<b>c</b>) compressive strength of chemical excitation.</p>
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<p>Changes in the hydration products of SFGE0.</p>
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<p>Variation in compressive strength of SFGC.</p>
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<p>Changes in the hydration products of SFGC.</p>
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<p>Changes in the hydration products of SFGC.</p>
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