scholarly journals Development of Strength for Calcium Aluminate Cement Mortars Blended with GGBS

2019 ◽  
Vol 2019 ◽  
pp. 1-12 ◽  
Author(s):  
Hee Jun Yang ◽  
Ki Yong Ann ◽  
Min Sun Jung

In the present study, the development of strength in different calcium aluminate cement (CAC) mixture mortars with granulated ground blast-furnace slag (GGBS) was investigated. The substitution of GGBS levels was 0, 20, 40, and 60% weight of binder, of which the CAC used in this study naturally contained C2AS clinker as a secondary phase. To activate a hydraulic nature of the phase, in addition to the mineral additive, all specimens were cured at 35 ± 2°C for the first 24 hours and then stored in a 95% humidity chamber at 25 ± 2°C. The penetration resistance of fresh mortar was measured immediately after pouring, and the mortar compressive strength was monitored for 365 days. Simultaneously, to evaluate the hydration kinetics at early ages, in terms of heat evolution, the calorimetric analysis was performed at the isothermal condition (35°C) for 24 hours. The hydration behavior in the long term was characterized by X-ray diffraction, which was supported by microscopic observation using scanning electron microscopy with energy dispersive spectroscopy. Furthermore, an examination of the pore structure was accompanied to quantify the porosity. As a result, it was found that an increase in the GGBS content in the mixture resulted in an increased setting time, as well as total heat evolved for 24 hours in normalized calorimetry curves. In addition, the strength development of mortar showed a continuous increased value up to 365 days, accounting 43.8–57.5 MPa for the mixtures, due to a formation of stratlingite, which was identified at the pastes cured for 365 days using chemical and microscopic analysis. However, GGBS replacement did not affect on the pore size distribution in the cement matrix, except for total intrusion volume.

2008 ◽  
Vol 35 (4) ◽  
pp. 400-407 ◽  
Author(s):  
Jincheol Kim ◽  
Jonghyun Ryu ◽  
R. D. Hooton

The influence of rapid-set accelerating admixtures on the setting behavior and early-age strength of a cement matrix was investigated to evaluate the appropriateness of the specification and test methods for shotcrete set accelerators. The results verified two different rapid setting behaviors according to the types of accelerator. The aluminate-base and the calcium aluminate cement-base accelerators facilitate hydration by formation of a calcium aluminate solid solution, whereas the alkali-free set accelerating agents present rapid setting time by the formation of ettringite. It was also found that the Vicat test was more desirable than the Gillmore test as the standard for setting time evaluation. Additionally, the cement mortar mixed with the aluminate-base and the calcium aluminate cement-base accelerators exhibited very fast development of early-age compressive strength. However, most of the set accelerators, except for alkali-free accelerators, failed to satisfy the specification because of greater than 40% compressive strength loss at 28 d.


2021 ◽  
Vol 2076 (1) ◽  
pp. 012035
Author(s):  
Yu Zhang ◽  
Jiahao Yang ◽  
Yu Liu ◽  
Bin Liu ◽  
Fengqing Zhao

Abstract The construction material from anhydrite-II phosphogypsum is dense in structure and has good water resistance. But its disadvantages are low hydration activity and long setting time. In this work, anhydrite-II phosphogypsum is modified by adding a composite activator, which is made of sulfuric acid modified steel slag, β-hemihydrate gypsum and calcium aluminate cement. With this, the hydration rate of anhydrite-II phosphogypsum is clearly increased and setting time shortened. The performance of self leveling mortar prepared is as per JC/T 1023-2021, with softening coefficient of 0.8.


2021 ◽  
pp. 1-29
Author(s):  
Sanghamitra Bharati ◽  
Manjini Sambandam ◽  
Pankaj Lochan

Strict environmental norms and raising concern to recycle solid wastes generated during ironmaking and steelmaking processes has been the key driving force in developing various technologies. The present study describes a calcium-aluminate clinker prepared from steel ladle slag by modifying its mineral compositions. The slag paste prepared by mixing with water exhibited flash setting behaviour due to the presence of C12A7 and C3A phases. In contrast, the slag clinker, developed by sintering a mixture of pre-determined quantity of slag and Al2O3 at 1400°C for 2h and 4h, contained CA, CA2, Gehlenite and ‘Q’ phases. Hydration of slag clinker contained stable C3AH6, AH3 and stratlingite with preferential growth of calcium-aluminate hydrate prisms along c-axis that provided a well-defined raceme like morphology with interlinked structure. It improved the setting time and crushing strength of the clinkers after 6h and 24h curing at room temperature. Additionally, presence of ‘Q’ phase with lamellar prismatic crystals also helped in enhancing the strength. The developed clinker also exhibited superior crushing strength as compared to commercially available calcium aluminate cement of medium purity. The slag, used as a source of CaO could replace CaCO3 completely and thus contributed to reduction in CO2 emission during clinker making process.


2004 ◽  
Vol 19 (4) ◽  
pp. 1062-1067 ◽  
Author(s):  
S.H. Oh ◽  
R. Finones ◽  
S. Jin ◽  
S.Y. Choi ◽  
K.N. Kim

The influence of tricalcium aluminate (3CaO·Al2O3) phase doping on in vitro biocompatibility and bioactivity of calcium aluminate (CaO·Al2O3) based bone cement has been investigated. It is demonstrated that the presence of approximately 25% tricalcium aluminate in the bone cement remarkably improves the bioactivity, yet still retains desirable mechanical strength and biocompatibility. An intermediary compound layer such as Ca3Al2(OH)12 was formed on the surface of the doped sample onto which hydroxyapatite (HAp) began to form soon, after only 2 days of immersion in a simulated body fluid solution. This is about seven-fold acceleration in the HAp formation over undoped calcium aluminate cement on which it took approximately15 days to nucleate the HAp phase. The depth of the HAp-containing layer after60 days of soaking was as much as 85 μm, about an order of magnitude more than the undoped calcium aluminate cement. The dramatically accelerated nucleation and growth of hydroxyapatite caused by the presence of tricalcium aluminate is attributed to the occurrence of intermediate layer materials such as Ca3Al2(OH)12, which most likely acts as the nuclei for HAp formation. This doped bone cement can be useful for injectable orthopedic applications, as the setting time for hardening has also been significantly reduced (by a factor of at least 4) to a practical regime of tens of minutes.


2016 ◽  
Vol 680 ◽  
pp. 455-461 ◽  
Author(s):  
Hao Dai ◽  
Shu Peng Zhang ◽  
Cheng Lan Ju ◽  
Dong Xu Li

The effect of calcium sulfates varieties on the properties of calcium aluminate cement-based self-leveling mortar have been investigated, and the hydration kinetics, hydrated products and microstructures are characterized by isothermal calorimeter, X-ray diffraction and mercury intrusion porosimetry, respectively. The results show that the technological properties of mortars are significantly affected by calcium sulfate varieties and content. The setting times are shortened drastically with the addition of calcium sulfates. Mortars with hemihydrate show higher early strength and less drying shrinkage. In contrast, using anhydrite in mortars cause lower strength and higher drying shrinkage at early age but larger growth of strength in the late. The increasing calcium sulfates content may result in the delay of main hydration peak in the heat evolution curve. For formulation with hemihydrate, the appearance of main hydration peaks are advanced compared with formulation without addition of calcium sulfates. Moreover, mortar microstructures are optimized by addition of β-hemihydrate, the proportion of large pores are lower than that of mortars with anhydrite.


2015 ◽  
Vol 154 ◽  
pp. 158-163 ◽  
Author(s):  
Boquan Zhu ◽  
Yanan Song ◽  
Xiangcheng Li ◽  
Pingan Chen ◽  
Zheng Ma

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