TL;DR: In this paper, the relationship between the microstructure and engineering properties of cement-treated marine clay was examined using x-ray diffraction, scanning electron microscopy, pH measurement, mercury intrusion porosimetry, and laser diffractometric measurement of the particle size distribution.
Abstract: This paper examines the relationship between the microstructure and engineering properties of cement-treated marine clay. The microstructure was investigated using x-ray diffraction, scanning electron microscopy, pH measurement, mercury intrusion porosimetry, and laser diffractometric measurement of the particle size distribution. The engineering properties that were measured include the water content, void ratio, Atterberg limit, permeability, and unconfined compressive strength. The results indicate that the multitude of changes in the properties and behavior of cement-treated marine clay can be explained by interaction of four underlying microstructural mechanisms. These mechanisms are the production of hydrated lime by the hydration reaction which causes flocculation of the illite clay particles, preferential attack of the calcium ions on kaolinite rather than on illite in the pozzolanic reaction, surface deposition and shallow infilling by cementitious products on clay clusters, as well as the presence of water trapped within the clay clusters.
TL;DR: In this article, the early stages of hydration of Portland cement Type I in the presence and absence of sodium lignosulfonate (a superplasticizer) have been investigated by Fourier transform infrared spectroscopic technique.
TL;DR: In this article, the carbonation behaviors of hydraulic and non-hydraulic calcium silicate phases, including tricalcium silicate (3CaO·SiO2 or C3S), γ-dical calcium silicates (γ-2C2S, β-C 2S, and β-c2S), rankinite (3CO·2SiO 2 or c3S2), and wollastonite (CaO•SiO•O 2 ) were investigated.
Abstract: This paper presents a study on the carbonation behaviors of hydraulic and non-hydraulic calcium silicate phases, including tricalcium silicate (3CaO·SiO2 or C3S), γ-dicalcium silicate (γ-2CaO·SiO2 or γ-C2S), β-dicalcium silicate (β-2CaO·SiO2 or β-C2S), rankinite (3CaO·2SiO2 or C3S2), and wollastonite (CaO·SiO2 or CS). These calcium silicate phases were subjected to carbonation reaction at different CO2 concentration and temperatures. Thermogravimetric analysis (TGA) tests were performed to quantify the amounts of carbonates formed during the carbonation reactions, which were eventually used to monitor the degree of reactions of the calcium silicate phases. Both hydraulic and non-hydraulic calcium silicates demonstrated higher reaction rate in case of carbonation reaction than that of the hydration reaction. Under specific carbonation scenario, non-hydraulic low-lime calcium silicates such as γ-C2S, C3S2 and CS were found to achieve a reaction rate close to that of C3S. Fourier transformed infrared (FTIR) spectroscopy and scanning electron microscope (SEM) tests were performed to characterize the carbonation reaction products of the calcium silicate phases. The FTIR spectra during the early stage of carbonation reaction showed formation of calcium silicate hydrate (C–S–H) from C3S, γ-C2S, β-C2S, and C3S2 phases with a similar degree of polymerization as that of the C–S–H that forms during the hydration reaction of C3S. However, upon further exposure to CO2, these C–S–H phases decompose and eventually converted to calcium-modified (Ca-modified) silica gel phase with higher degree of silicate polymerization. Contradictorily, CS phase started forming Ca-modified silica gel phase even at the early stage of carbonation reaction. This paper also revealed the stoichiometry of the Ca-modified silica gel that formed during the carbonation reaction of the calcium silicate phases using the SEM/energy dispersive spectroscopy (EDS) and TGA results.
TL;DR: In this article, the effect of bovine carbonic anhydrase on the hydration of CO2 and its precipitation in the form of calcium carbonate, was studied.
Abstract: Biological sequestration of carbon dioxide (CO2) in geological formations is one of the proposed methods to reduce the carbon dioxide released into the atmosphere. In this method, an enzyme is used to enhance the hydration and subsequent precipitation of CO2. In the present work, the effect of bovine carbonic anhydrase on the hydration of CO2, and its precipitation in the form of calcium carbonate, was studied. The enzyme enhanced the hydration reaction. The rate of hydration reaction increased with both the enzyme concentration and temperature. The precipitation of calcium carbonate was promoted in the presence of the enzyme. The concentration of the enzyme did not affect the precipitation; however, temperature impacted the precipitation of calcium carbonate. At higher temperatures, less calcium carbonate was formed. Also, in the presence of the enzyme, calcium carbonate settled more quickly. The enzyme activity was not influenced by the pH of the reaction mixture. In contrast, the formation of calcium c...
TL;DR: In this paper, the effects of graphene oxide nanosheets with different sizes and dosages on cement hydration crystal shapes and the mechanical strength of cement paste are investigated, and it is found that flower-like crystals are more prominent at low GO dosage (0.03%).