Chemical and Microstructural Properties of Designed Cohesive M-S-H Pastes

Concretes can be exposed to a magnesium attack in several environments leading to the formation of magnesium silicate hydrates (M-S-H) and brucite (MH). The formation of M-S-H is likely to alter the properties of the cement matrix because it is linked to the decalcification of C-S-H. However, relatively few data on M-S-H exist in the literature. In order to characterize, physically and mechanically, the M-S-H phase, pure M-S-H cohesive pastes are needed. This work studies the formation of cohesive M-S-H pastes made with MgO-to-SiO2 atomic ratios of 0.78, 1 and 1.3, from two types of silica (silica fume or colloidal silica) and under 20 °C and 50 °C thermal curing. X-ray diffraction and thermogravimetric analyses confirmed that the consumption of brucite and the formation of M-S-H were quicker with a 50 °C curing. Energy-dispersive X-ray spectroscopy and microtomography showed that colloidal silica enabled a better distribution of the particles than silica fume. Microstructural characterizations were conducted under the protocol with colloidal silica and 50 °C thermal curing. Porosity investigations allowed to describe the M-S-H pastes as highly porous materials with a low content of micropores in comparison with mesopores. The type of mixing influenced the mesopore size distribution.

Effect of Aluminum Incorporation on the Reaction Process and Reaction Products of Hydrated Magnesium Silicate

In this study, we investigated the impact of aluminium ion (Al3+) incorporation on the microstructure and the phase transformation of the magnesium silicate hydrate system. The magnesium silicate hydrate system with aluminium was prepared by mixing magnesium oxide and silica fume with different aluminium ion contents (the Al/Si molar ratios of 0.01, 0.02, 0.05, 0.1, 0.2) at room temperature. The high degree of polymerization of the magnesium silicate hydrate phases resulted in the limited incorporation of aluminium in the structure of magnesium silicate hydrate. The silicon-oxygen tetrahedra sites of magnesium silicate hydrate layers, however, were unable to substitute for silicon sites through inverted silicon-oxygen linkages. The increase in aluminium ion content raised the degree of polymerization of the magnesium silicate hydrate phases from 0.84 to 0.92. A solid solution was formed from residual aluminum-amorphous phases such as hydroxyl-aluminum and magnesium silicate hydrate phases. X-ray diffraction (XRD), field emission scanning electron microscope (F-SEM), and 29Si and 27Al MAS NMR data showed that the addition of Al3+ promotes the hydration process of MgO and has an obvious effect on the appearance of M-S-H gel. The gel with low aluminum content is fluffy, while the gel with high aluminum content has irregular flakes. The amount of Al3+ that enters the M-S-H gel increased with the increase of Al3+ content, but there was a threshold: the highest Al/Si molar ratio of M-S-H gel can be maintained at about 0.006.

The integrity of synthetic magnesium silicate in charged compounds

Magnesium silicate is an inorganic compound used as an ingredient in product formulations for many different purposes. Since its compatibility with other components is critical for product quality and stability, it is essential to characterize the integrity of magnesium silicate in different solutions used for formulations. In this paper, we have determined the magnitude of dissociation of synthetic magnesium silicate in solution with positively charged, neutral, and negatively charged compounds using Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS), and Liquid Chromatography-High Resolution Mass Spectrometry (LC-HRMS). The EDS results were verified through Monte Carlo simulations of electron-sample interactions. The compounds chosen for this study were positively charged cetylpyridinium chloride (CPC), neutral lauryl glucoside, and negatively charged sodium cocoyl glutamate and sodium cocoyl glycinate since these are common compounds used in personal care and oral care formulations. Negatively charged compounds significantly impacted magnesium silicate dissociation, resulting in physio-chemical separation between magnesium and silicate ions. In contrast, the positively charged compound had a minor effect on dissociation due to ion competition, and the neutral compound did not have such an impact on magnesium silicate dissociation. Further, when the magnesium ions are dissociated from the synthetic magnesium silicate, the morphology is changed accordingly, and the structural integrity of the synthetic magnesium silicate is damaged. The results provide scientific confidence and guidance for product development using synthetic magnesium silicate.

Optical Properties and Radiation Stability of Magnesium Silicate

A microwave (MW) method of hydrothermal synthesis of magnesium silicate is developed. At low temperature (240 0C), nuclei of crystalline phase of магний silicate are obtained. Some optical characteristics of the synthesized product are determined. Based on, X-ray and thermographic studies are revealed that the synthesis of magnesium silicate from water-soluble salts of initial components in microwave ovens promotes the formation of magnesium at lower temperatures. MW synthesis of magnesium silicate ensures obtaining of nanosized powder after heat treatment at 850 0C.

Effects of Disodium Hydrogen Phosphate Addition and Heat Treatment on the Formation of Magnesium Silicate Hydrate Gel

The formation of magnesium silicate hydrate gel is crucial in preventing magnesia aggregates from over hydrated during the construction of refractory castables since the presence of magnesium hydroxide diminish the mechanical properties of the material. This work aimed to investigate the accelerating effects of sodium hydrogen phosphate and heat treatment on the formation of magnesium silicate hydrate gel. Time-dependent pH of magnesia - silica fume slurries with and without sodium hydrogen phosphate addition and heat treatment was measured to verify the dissolution of MgO and magnesium silicate hydrate formation. The effects of sodium hydrogen phosphate were differentiable only at small added amounts, whereas heat treatment at 50 degrees Celsius performed noticeable acceleration. This observation could be applicable in molding to maintain the stability of basic refractory castables.

A New Perspective on Adsorbent Materials Based Impregnated MgSiO3 with Crown Ethers for Palladium Recovery

The study of new useful, efficient and selective structures for the palladium ions’ recovery has led to the development of a new series of macromolecules. Thus, this study presents a comparative behavior of two crown benzene ethers that modify the magnesium silicate surface used as adsorbent for palladium. These crown ethers are dibenzo18-crown-6 (DB18C6) and dibenzo 30-crown-10 (DB30C10). The obtained materials were characterized by scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX) and Fourier-transform infrared spectroscopy (FT-IR). The specific surface area (BET) and point of zero charge (PZC) of the two materials were determined. The palladium ions’ recovery from synthetic aqueous solutions studies aimed to establish the adsorption mechanism. For this desideratum, the kinetic, equilibrium and thermodynamic studies show that MgSiO3-DB30C10 have a higher adsorption capacity (35.68 mg g−1) compared to MgSiO3-DB18C6 (21.65 mg g−1). Thermodynamic studies highlight that the adsorption of Pd(II) on the two studied materials are spontaneous and endothermic processes. The positive values of the entropy (ΔS0) suggest that the studied adsorption processes show a higher disorder at the liquid/solid interface. Desorption studies were also performed, and it was found that the degree of desorption was 98.3%.

Extraction of magnesium from salt pond waste with low lithium grade using sodium silicate reagent

Nowadays, Indonesia’s salt production process has shifted from a traditional salt pond process to a salt pond with a geomembrane tarpaulin system. This system has the advantage of producing a faster salting process and a better salt quality and producing a thick yellow liquid waste known as bittern. The waste produced has not been fully utilized, even though the waste contains valuable elements, namely magnesium, lithium, and others. This paper investigates the potential utilization of bittern by extracting magnesium from by-product salt pond using sodium silicate reagent with various concentrations of 125–250 g/l. The bittern used in this experiment had the chemical composition as follows: 33,184 ppm magnesium (Mg), 23,787 ppm sodium (Na), 6.1 ppm lithium (Li), 5,491 ppm potassium (K), 617 ppm calcium (Ca), 152 ppm boron (B). The highest removal of magnesium ion by addition of sodium silicate of 250 g/l was about 96.2%. The results showed that the solid products were magnesium silicate precipitates without containing asbestos compounds. The magnesium silicate precipitate product can be applied as talc raw material for the pharmaceutical industry.