Influence of Silica Fume Source on Crystallization of Xonotlite in a New Process Making Medium Density Ca-Silicate Based Products

2018 ◽  
Vol 788 ◽  
pp. 3-12
Author(s):  
Felipe Marti-Montava ◽  
Ann Opsommer ◽  
David Garcia-Sanoguera

This paper investigates the influence of different types of silica fume on the crystallization process of medium density calcium silicate based products. The products are formed by a new technology that consists of two steps. In the first step, a mixture containing calcium silicate hydrates (C-S-H) is formed by reaction of lime with special silicas at temperatures below 100°C. This mixture is then molded into boards by a filter-pressing technique. In the second step, the boards are treated in hydrothermal conditions enabling the conversion of the C-S-H into important contents of xonotlite (Ca6Si6O17(OH)2); this is the most stable calcium silicate hydrate phase at high temperatures. In order to make C-S-H in pressure less conditions, the use of reactive forms of silica is required. In this work we used silica fume as reactive silica. To understand the influence of the silica fume on the formation of xonotlite, several properties were studied, such as particle size, purity and specific surface area (BET). It was found that the particle size distribution and degree of agglomeration for the silica fume were the most important properties. A proper dispersion technique must be applied in order to break the silica fume agglomerates, forming particles small enough to react with dissolved lime and to form C-S-H phases that are able to be converted into xonotlite under hydrothermal conditions. Finally, it was also found that the formation of xonotlite is favored by the use of high purity silica fume.

Nanomaterials ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 1299
Author(s):  
Domante Niuniavaite ◽  
Kestutis Baltakys ◽  
Tadas Dambrauskas ◽  
Anatolijus Eisinas ◽  
Dovile Rubinaite ◽  
...  

In this work, the thermal stability, microstructure, and catalytic activity in oxidation reactions of calcium silicate hydrates formed in the CaO-SiO2-Cr(NO3)3-H2O system under hydrothermal conditions were examined in detail. Dry primary mixture with a molar ratio of CaO/SiO2 = 1.5 was mixed with Cr(NO3)3 solution (c = 10 g Cr3+/dm3) to reach a solution/solid ratio of the suspension of 10.0:1. Hydrothermal synthesis was carried out in unstirred suspensions at 175 °C for 16 h. It was determined that, after treatment, semicrystalline calcium silicate hydrates C-S-H(I) and/or C-S-H(II) with incorporated Cr3+ ions (100 mg/g) were formed. The results of in situ X-ray diffraction and simultaneous thermal analyses showed that the products were stable until 500 °C, while, at higher temperatures, they recrystallized to calcium chromate (CaCrO4, 550 °C) and wollastonite (800–850 °C). It was determined that both the surface area and the shape of the dominant pore changed during calcination. Propanol oxidation experiments showed that synthetic semicrystalline calcium silicate hydrates with intercalated chromium ions are able to exchange oxygen during the heterogeneous oxidation process. The obtained results were confirmed by XRD, STA, FT-IR, TEM, SEM, and BET methods, and by propanol oxidation experiments.


2019 ◽  
Vol 198 ◽  
pp. 218-225 ◽  
Author(s):  
G.M. Kim ◽  
Y.K. Kim ◽  
Y.J. Kim ◽  
J.H. Seo ◽  
B.J. Yang ◽  
...  

RSC Advances ◽  
2018 ◽  
Vol 8 (49) ◽  
pp. 28198-28208 ◽  
Author(s):  
Xiaoling Qu ◽  
Zhiguang Zhao ◽  
Xuguang Zhao

The phase assembly and microstructure of the aluminum-incorporated CaO–SiO2–H2O system were investigated using XRD, SEM, FTIR and NMR depending on aluminum addition, reaction temperature and curing time.


2000 ◽  
Vol 18 (3) ◽  
pp. 195-204
Author(s):  
E.E. Hekal ◽  
N.A. Mousa

The effect of sodium naphthalene formaldehyde sulphonate polycondensate and stearic acid on the surface properties of calcium silicate hydrates, formed as a result of the hydration reaction between silica fume and calcium hydroxide, has been examined by the use of low-temperature nitrogen gas adsorption techniques. In addition, the interaction of such admixtures with the calcium silicate hydrates formed was investigated by infrared (IR) spectroscopic analysis. It was observed that both admixtures increased the specific surface area of the calcium silicate hydrates quite considerably relative to the behaviour of a blank sample (i.e. without addition of admixture), especially during the initial stages of hydration (after 24 h). IR examination demonstrated that the admixtures used did not interact chemically with the calcium silicate hydrates although physical interaction was possible.


2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Lu Zeng ◽  
Ligang Yang ◽  
Shuping Wang ◽  
Kai Yang

Different crystalline calcium silicate hydrates (CSH) were synthesized under specific hydrothermal conditions and several methods were used to analyze samples. Amorphous calcium silicate hydrates (ACSH) mainly consists of disordered calcium silicate hydrate gel (C-S-H gel) and crystalline calcium silicate hydrates (CCSH) consists of crystallized tobermorite. The adsorption of carcinogenic aflatoxin B1 (AFB1) onto ACSH and CCSH was investigated. The adsorption kinetics was studied using pseudo-first-order and pseudo-second-order kinetic models and intraparticle diffusion model. The pseudo-second-order model provided the best correlation and the intraparticle diffusion controlled the adsorption process of AFB1 onto CCSH. Adsorption isotherm parameters were obtained from Langmuir and Freundlich and the adsorption data fitted to Freundlich much better. Based on the results of N2adsorption/desorption, adsorption kinetics, and adsorption isotherms, the adsorption mechanism of AFB1 onto CCSH was developed. All results indicate that CCSH has a great potential to be a safe, easy-made, and cost-effective material for the control of AFB1 contamination.


Langmuir ◽  
2015 ◽  
Vol 31 (13) ◽  
pp. 3779-3783 ◽  
Author(s):  
Julio C. da Silva ◽  
Pavel Trtik ◽  
Ana Diaz ◽  
Mirko Holler ◽  
Manuel Guizar-Sicairos ◽  
...  

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