Structural concrete based on alkali-activated binders: Terminology, reaction mechanisms, mix designs and performance

2017 ◽  
Vol 19 (3) ◽  
pp. 918-929 ◽  
Author(s):  
Annemarie Herrmann ◽  
Andreas Koenig ◽  
Frank Dehn
Keyword(s):  
Reaction Mechanisms ◽  
Structural Concrete ◽  
And Performance ◽  
Alkali Activated Binders ◽  
Alkali Activated

scholarly journals Insights into the Microstructure of Hydrothermal Synthesized Nanoscale K2O-Al2O3-SiO2-H2O Particles

Nanomaterials ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 63 ◽  
Author(s):  
Liu ◽  
Zhu ◽  
Zhuang ◽  
Shuai ◽  
Li ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Surface Area ◽  
Three Dimensional ◽  
Structural Rearrangement ◽  
Curing Temperature ◽  
Bet Surface Area ◽  
Transmission Electron ◽  
And Performance ◽  
Alkali Activated Binders ◽  
Alkali Activated

K-A-S-H (K2O-Al2O3-SiO2-H2O) gel is a key phase that forms in most alkali-activated binders (eco-friendly binders which utilize a substantial amount of industrial by-product). An in-depth understanding of the microstructure and performance of this nano-sized key phase facilitates better application to alkali-activated binders. However, such studies remain little and undetailed. Therefore, our research aims to provide insights into the microstructure of K-A-S-H particles synthesized with accurate stoichiometric control by the hydrothermal method through thermogravimetric analysis (TG), Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and BET surface area. The results show that for materials prepared at the curing temperature lower than 80 °C, the K-A-S-H products were completely amorphous. With increased curing temperature and time, the K-A-S-H products were transformed from the amorphous phase to the crystalline zeolite phase structure, with a reduction in the specific surface area. The TG results indicate that the crystalline phase contains more non-evaporated water or zeolite water for structural rearrangement. The degree of tetrahedral polymerization slightly decreased with an increase of the K2O/SiO2 ratio as the amount of non-bridged oxygen atoms increased, whereas it gradually increased with an increase of curing temperature and time, as suggested by the FTIR and NMR results. Various K2O/SiO2 ratios resulted in the formation of zeolite K-H and K-G zeolite, both of which exhibited highly polymerized three-dimensional network structures. However, there was no significant effect of the SiO2/Al2O3 ratio on the structure of K-A-S-H products. Overall, these results provide insight into understanding the chemical stability of K-A-S-H.

scholarly journals Alkali-Activated Binders Using Bottom Ash from Waste-to-Energy Plants and Aluminium Recycling Waste

2021 ◽  
Vol 11 (9) ◽  
pp. 3840 ◽  
Author(s):  
Alex Maldonado-Alameda ◽  
Jofre Mañosa ◽  
Jessica Giro-Paloma ◽  
Joan Formosa ◽  
Josep Maria Chimenos
Keyword(s):  
Bottom Ash ◽  
Physicochemical Characterization ◽  
Waste To Energy ◽  
Promising Alternative ◽  
Leaching Potential ◽  
Aluminium Recycling ◽  
Alkaline Activator ◽  
Alkali Activated Binders ◽  
Energy Plants ◽  
Alkali Activated

Alkali-activated binders (AABs) stand out as a promising alternative to replace ordinary Portland cement (OPC) due to the possibility of using by-products and wastes in their manufacturing. This paper assessed the potential of weathered bottom ash (WBA) from waste-to-energy plants and PAVAL® (PV), a secondary aluminium recycling process by-product, as precursors of AABs. WBA and PV were mixed at weight ratios of 98/2, 95/5, and 90/10. A mixture of waterglass (WG) and NaOH at different concentrations (4 and 6 M) was used as the alkaline activator solution. The effects of increasing NaOH concentration and PV content were evaluated. Alkali-activated WBA/PV (AA-WBA/PV) binders were obtained. Selective chemical extractions and physicochemical characterization revealed the formation of C-S-H, C-A-S-H, and (N,C)-A-S-H gels. Increasing the NaOH concentration and PV content increased porosity and reduced compressive strength (25.63 to 12.07 MPa). The leaching potential of As and Sb from AA-WBA/PV exceeded the threshold for acceptance in landfills for non-hazardous waste.

Advances in MXene Films: Synthesis, Assembly, and Applications

2021 ◽  
Author(s):  
Xiaohua Li ◽  
Feitian Ran ◽  
Fan Yang ◽  
Jun Long ◽  
Lu Shao
Keyword(s):  
Spin Coating ◽  
Reaction Mechanisms ◽  
Membrane Separation ◽  
Synthesis Methods ◽  
Metal Carbides ◽  
Max Phases ◽  
Practical Applications ◽  
Coating Methods ◽  
And Performance ◽  
Important Form

AbstractA growing family of two-dimensional (2D) transition metal carbides or nitrides, known as MXenes, have received increasing attention because of their unique properties, such as metallic conductivity and good hydrophilicity. The studies on MXenes have been widely pursued, given the composition diversity of the parent MAX phases. This review focuses on MXene films, an important form of MXene-based materials for practical applications. We summarized the synthesis methods of MXenes, focusing on emerging synthesis strategies and reaction mechanisms. The advanced assembly technologies of MXene films, including vacuum-assisted filtration, spin-coating methods, and several other approaches, were then highlighted. Finally, recent progress in the applications of MXene films in electrochemical energy storage, membrane separation, electromagnetic shielding fields, and burgeoning areas, as well as the correlation between compositions, architecture, and performance, was discussed.

scholarly journals Effect of CaSO4 Incorporation on Pore Structure and Drying Shrinkage of Alkali-Activated Binders

Materials ◽  
2019 ◽  
Vol 12 (10) ◽  
pp. 1673 ◽  
Author(s):  
Hyeongmin Son ◽  
Sol Moi Park ◽  
Joon Ho Seo ◽  
Haeng Ki Lee
Keyword(s):  
Fly Ash ◽  
Pore Structure ◽  
Drying Shrinkage ◽  
Phase Changes ◽  
X Ray Diffraction ◽  
Activated Slag ◽  
Capillary Tension ◽  
Alkali Activated Binders ◽  
Internal Pore Structure ◽  
Alkali Activated

This present study investigates the effects of CaSO4 incorporation on the pore structure and drying shrinkage of alkali-activated slag and fly ash. The slag and fly ash were activated at a 5:5 ratio by weighing with a sodium silicate. Thereafter, 0%, 5%, 10%, and 15% of CaSO4 were incorporated to investigate the changes in phase formation and internal pore structure. X-Ray Diffraction (XRD), thermogravimetry (TG)/derivative thermogravimetry (DTG), mercury intrusion porosimetry (MIP), nuclear magnetic resonance (NMR), and drying shrinkage tests were carried out to find the correlation between the pore structure and drying shrinkage of the specimens. The results showed that CaSO4 incorporation increased the formation of thenardite, and these phase changes affected the pore structure of the activated fly ash and slag. The increase in the CaSO4 content increased the pore distribution in the mesopore. As a result, the capillary tension and drying shrinkage decreased.

scholarly journals Leaching, carbonation and chloride ingress in reinforced alkali-activated fly ash mortars

2018 ◽  
Vol 199 ◽  
pp. 02025 ◽  
Author(s):  
Gregor J. G. Gluth ◽  
Petr Hlaváček ◽  
Steffi Reinemann ◽  
Gino Ebell ◽  
Jürgen Mietz
Keyword(s):  
Fly Ash ◽  
Visual Inspection ◽  
Electrochemical Behaviour ◽  
Transport Coefficients ◽  
Chloride Penetration ◽  
Chloride Ingress ◽  
Reaction Products ◽  
Steel Bars ◽  
Alkali Activated Binders ◽  
Alkali Activated

Alkali-activated fly ash mortars were studied with regard to durability-relevant transport coefficients and the electrochemical behaviour of embedded carbon steel bars on exposure of the mortars to leaching, carbonation and chloride penetration environments. The transport coefficients differed considerably between different formulations, being lowest for a mortar with BFS addition, but still acceptable for one of the purely fly ash-based mortars. Leaching over a period of ~300 days in de-ionized water did not lead to observable corrosion of the embedded steel, as shown by the electrochemical data and visual inspection of the steel. Exposure to 100 % CO2 atmosphere caused steel depassivation within approx. two weeks; in addition, indications of a deterioration of the mortar were observed. The results are discussed in the context of the different reaction products expected in highand low-Ca alkali-activated binders, and the alterations caused by leaching and carbonation.

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