scholarly journals Formation of Geopolymers Using Sodium Silicate Solution and Aluminum Orthophosphate

Materials ◽  
2020 ◽  
Vol 13 (18) ◽  
pp. 4202
Author(s):  
Stephan Partschefeld ◽  
Torben Wiegand ◽  
Frank Bellmann ◽  
Andrea Osburg
Keyword(s):  
Sodium Silicate ◽  
Ph Value ◽  
Sodium Silicate Solution ◽  
Silicate Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Amorphous Phases ◽  
Amorphous Aluminosilicate ◽  
Kinetics Of ◽  
Aluminum Orthophosphate

This paper reports the formation and structure of fast setting geopolymers activated by using three sodium silicate solutions with different modules (1.6, 2.0 and 2.4) and a berlinite-type aluminum orthophosphate. By varying the concentration of the aluminum orthophosphate, different Si/Al-ratios were established (6, 3 and 2). Reaction kinetics of binders were determined by isothermal calorimetric measurements at 20 °C. X-ray diffraction analysis as well as nuclear magnetic resonance (NMR) measurements were performed on binders to determine differences in structure by varying the alkalinity of the sodium silicate solutions and the Si/Al-ratio. The calorimetric results indicated that the higher the alkalinity of the sodium silicate solution, the higher the solubility and degree of conversion of the aluminum orthophosphate. The results of X-ray diffraction and Rietveldt analysis, as well as the NMR measurements, confirmed the assumption of the calorimetric experiments that first the aluminum orthophosphate was dissolved and then a polycondensation to an amorphous aluminosilicate network occurred. The different amounts of amorphous phases formed as a function of the alkalinity of the sodium silicate solution, indicate that tetrahydroxoaluminate species were formed during the dissolution of the aluminum orthophosphate, which reduce the pH value. This led to no further dissolution of the aluminum orthophosphate, which remained unreacted.

scholarly journals Pressure-Induced Geopolymerization in Alkali-Activated Fly Ash

2018 ◽  
Vol 10 (10) ◽  
pp. 3538 ◽  
Author(s):  
Sol Park ◽  
Hammad Khalid ◽  
Joon Seo ◽  
Hyun Yoon ◽  
Hyeong Son ◽  
...  
Keyword(s):  
Fly Ash ◽  
Sodium Hydroxide ◽  
Sodium Silicate ◽  
Sodium Silicate Solution ◽  
Silicate Solution ◽  
Elevated Pressure ◽  
X Ray Diffraction ◽  
27Al Mas Nmr ◽  
Alkali Activated

The present study investigated geopolymerization in alkali-activated fly ash under elevated pressure conditions. The fly ash was activated using either sodium hydroxide or a combination of sodium silicate solution and sodium hydroxide, and was cured at 120 °C at a pressure of 0.22 MPa for the first 24 h. The pressure-induced evolution of the binder gel in the alkali-activated fly ash was investigated by employing synchrotron X-ray diffraction and solid-state 29Si and 27Al MAS NMR spectroscopy. The results showed that the reactivity of the raw fly ash and the growth of the zeolite crystals were significantly enhanced in the samples activated with sodium hydroxide. In contrast, the effects of the elevated pressure conditions were found to be less apparent in the samples activated with the sodium silicate solution. These results may have important implications for the binder design of geopolymers, since the crystallization of geopolymers relates highly to its long-term properties and functionality.

Thermodynamics and Kinetics of Crystal-Amorphous Transformation in A1–x Bx Alloys During Reaction with Hydrogen

1985 ◽  
Vol 58 ◽  
Author(s):  
X. L. Yeh ◽  
W. L. Johnson ◽  
J. Y. Tang ◽  
C. R. Shi ◽  
W. M. Keck
Keyword(s):  
Amorphous Phase ◽  
Hydrogen Permeation ◽  
Depth Profiling ◽  
Sample Surface ◽  
Hydride Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Amorphous Phases ◽  
Kinetics Of ◽  
Amorphous Phase Formation

ABSTRACTThe kinetics of amorphous phase formation in polycrystalline A1–xBx (A=Zr, Hf, B=Pd, Rh,.15<x<.25) alloys during reaction with hydrogen has been studied by x-ray diffraction, +19F nuclear reaction depth profiling, TEM and electron diffraction. The formation of the amorphous hydride phase is observed by TEM to begin at grain bounderies of the polycrystalline Zr1–xRhx much in the same manner that “melting” nucleates at grain boundaries. TEM micrographs further show that the phase boundary between the crystalline and amorphous phases remains sharp during the growth of the amorphous phase. Both x-ray diffraction and nuclear depth profiling studies suggest that the overall rate of transformation to the amorphous hydride phase is limited by the rate of hydrogen permeation through the sample surface.Based on the present experiments and an analysis of the relevant free energy curves, we discuss the thermodynamic and kinetic aspects of this effect to explain why an amorphous phase is formed.

Synthesis of Silica Materials from the Slurry Waste

2018 ◽  
Vol 765 ◽  
pp. 79-82 ◽  
Author(s):  
Zih Yao Shen ◽  
Zhong Chen Lu ◽  
Yun Chi Liu ◽  
Maw Tien Lee
Keyword(s):  
Silicon Carbide ◽  
Sodium Silicate ◽  
Liquid Mixture ◽  
Sol Gel ◽  
Sodium Silicate Solution ◽  
Silicate Solution ◽  
X Ray Diffraction ◽  
Fourier Transformation Infrared Spectroscopy ◽  
Solar Energy Industry ◽  
Silicon Silicon

In solar energy industry, large amount of slurry wastes were produced during the wafer dicing process. The slurry waste contains silicon, silicon carbide and cutting oil. In this study, silicon in the slurry waste was treated with sodium hydroxide to produce a liquid mixture of the sodium silicate. The residue of the reaction was silicon carbide. The liquid mixture was separated to be a sodium silicate solution and used as a silica precursor for producing the silica powder and a hydrophobic silica aerogel by using the sol-gel method. The products were characterized by Fourier transformation infrared spectroscopy (FTIR) and powder X-ray diffraction (pXRD). Experimental results show that the characteristics of the products produced from the slurry waste are similar to that obtained by using the pure sodium silicate solution. It indicates that the wafer dicing slurry waste has a high potential to be a resource for other industries.

An Exploration of Factors Affecting the Preparation of SiO2-Coated α-Al2O3 Pearlescent Pigment

2014 ◽  
Vol 983 ◽  
pp. 26-29
Author(s):  
Nan Wu ◽  
Qing Hua Chen ◽  
Wei Ming Zhou ◽  
Mei Zhen Ke ◽  
Qing Rong Qian ◽  
...  
Keyword(s):  
Sodium Silicate ◽  
Reaction Temperature ◽  
Ph Value ◽  
Sodium Silicate Solution ◽  
Silicate Solution ◽  
Liquid Phase Deposition ◽  
Factors Affecting ◽  
Solution Reaction ◽  
Pearlescent Pigment

The SiO2-coated α-Al2O3 pearlescent pigment was prepared by liquid phase deposition (LPD). The effects of concentration of sodium silicate solution, reaction temperature and pH value of the aluminum oxide suspending liquid were systemically studied in this paper. The obtained samples were characterized by scanning electron microscopy (SEM). The results showed that when the process parameters are the concentration of sodium silicate solution of 0.1 mol/L, the reaction temperature of 80 °C and the pH value of 9.0, the high quality of SiO2-coated α-Al2O3 pearlescent pigment could be obtained.

scholarly journals JOINT TREATMENT OF BENTONITES WITH INORGANIC POLYELECTROLYTES AND CATIONIC SURFACTANTS IN ORDER TO PROMOTE ORGANOCLAY EXFOLIATION

2019 ◽  
Vol 62 (5) ◽  
pp. 71-77
Author(s):  
Viktor A. Gerasin ◽  
Viktor V. Kurenkov
Keyword(s):  
Polymer Composites ◽  
Sodium Silicate ◽  
Young Modulus ◽  
Sodium Silicate Solution ◽  
Silicate Solution ◽  
X Ray Diffraction ◽  
New Approach ◽  
Polymer Properties ◽  
Activated Bentonite ◽  
Set Up

A new approach to production of organomodified bentonites is offered. Bentonites are consecutively treated with inorganic polyelectrolyte (sodium silicate solution) and quaternary ammonium salts, as a result exfoliated organoclays are obtained. An ejector set up has been used for treatment of natural bentonites. Samples of activated bentonites treated in the ejector set up with sodium silicate solution (up to 21 g of sodium silicate per 100 g of bentonite) were prepared. Structure of the obtained bentonite and organoclay samples was established by X-ray diffraction analysis. It has been shown that treatment of the activated bentonite with sodium silicate does not influence the structure of the non-modified bentonite particles, but facilitates exfoliation of clay after organomodification. Polymer composites based on EVA containing 5% wt. of bentonites were prepared by extrusion mixing. In case of non-modified bentonites microcomposites are formed. In case of organomodified bentonites, not treated with sodium silicate, intercalated nanocomposites are formed. Treatment of bentonite with sodium silicate solution and subsequent organomodification ensures the production of exfoliated nanocomposite. Mechanical properties of obtained polymer composites were determined. Incorporation of 5% wt. clays or organoclays into the polymer material leads to increase in Young modulus (up to 50%), tensile strength (up to 20%); elongation at break decreases by 10% or less. In order to ensure the more significant reinforcing effect in EVA composites optimization of the organomodified bentonite composition (selection of surfactant and its content in the organoclay) has to be carried out with account for the polymer properties.

The Effect of Milling Time on the Size of Silica Particles from Silica Sand

2018 ◽  
Vol 917 ◽  
pp. 162-166 ◽  
Author(s):  
Agus Ismail ◽  
Insan Akbar Alamsyah ◽  
Muhammad Kholil ◽  
Bambang Heru Susanto ◽  
Mohamad Nasikin
Keyword(s):  
Silica Nanoparticles ◽  
Sodium Silicate ◽  
Milling Time ◽  
Sol Gel ◽  
Sodium Silicate Solution ◽  
Silicate Solution ◽  
High Energy ◽  
Silica Sand ◽  
X Ray Diffraction ◽  
Sol Gel Process

We report a method to adjust the size of silica nanoparticles from silica sand. In this study, synthesized silica nanoparticles by sol gel process from silica sand were conducted, with previously was controlled the size of silica sand by mechanical milling. Silica sand was milled by High Energy Milling in order to reduce the size into powder form. Effect of milling time shown the content of sodium and silicon is increased in sodium silicate solution obtained from various times of silica sand milling (30, 60 and 90 minutes, respectively) which is reacted with sodium hydroxide 8 M. The result of silica nanoparticles from sol gel process of sodium silicate solution were characterized using atomic absorption spectroscopy, scanning electron microscopy and X-ray diffraction techniques. It was found that the size of silica nanoparticles could be tailored with the change of milling time.

The Effect of Activators on the Fly Ash-Based Geopolymers

2011 ◽  
Vol 477 ◽  
pp. 85-90
Author(s):  
Yun Fen Hou ◽  
Dong Min Wang
Keyword(s):  
Compressive Strength ◽  
Fly Ash ◽  
Sodium Silicate ◽  
Sodium Silicate Solution ◽  
Solution Concentration ◽  
Silicate Solution ◽  
Strength Development ◽  
X Ray Diffraction ◽  
Sodium Potassium ◽  
Class F Fly Ash

This paper studies the influences of concentration and modulus of sodium silicate solution (Na activator) and sodium potassium silicate solution (Na-K activator) on the phase composition, microstructure and strength development in the geopolymers prepared using Class F fly ash. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and MAS NMR were utilized. It shows that the compressive strength increases while Na activator solution modulus increases, but when modulus exceeds 1.4, the compressive strength decreases, and it decreases markedly while modulus is greater than 2.0. The compressive strength improves with increase of sodium silicate solution concentration, and when concentration is 32%, compressive strength reaches the maximum, and then it reduces with concentration increment. It shows that the compressive strength increases while Na-K activator solution modulus increases, but when modulus exceeds 1.7, the compressive strength decreases, and it decreases markedly while modulus is greater than 2.0. The compressive strength improves with increase of Na-K activator solution concentration, and when concentration is 36%, compressive strength reaches the maximum. The main product of reaction in the geopolymeric material is amorphous alkali aluminosilicate gel.

Leaching Studies of Cement-Glass Package Containing Sodium Borate

1986 ◽  
Vol 84 ◽  
Author(s):  
Masahiro Okamoto ◽  
Koichi Chino ◽  
Tsutomu Baba ◽  
Tatsuo Izumida ◽  
Fumio Kawamura ◽  
...  
Keyword(s):  
Sodium Silicate ◽  
Liquid Waste ◽  
Sodium Borate ◽  
Pressurized Water Reactor ◽  
X Ray Diffraction ◽  
Adsorption Ability ◽  
Pressurized Water ◽  
X Ray ◽  
Solidification Reaction ◽  
Main Components

AbstractA new solidification technique using cement-glass, which is a mixture of sodium silicate, cement, additives, and initiator of the solidification reaction, was developed for sodium borate liquid waste generated from pressurized water reactor (PWR) plants. The cement-glass could solidify eight times as much sodium borate as cement could, because the solidifying reaction of the cement-glass is not hindered by borate ions.The reaction mechanism of sodium silicate and phosphoric silicate (initiator), the main components of cement-glass, was studied through X-ray diffraction and compressive strength measurements. It was found that three- dimensionally bonded silicon dioxide was produced by polymerization of the two silicates. The leaching ratio of cesium from the cement-glass package was one-tenth that of the cement one. This low value was attributed to a high cesium adsorption ability of the cement-glass and it could be theoretically predicted accordingly.

scholarly journals Stable and Metastable Phase Equilibria Involving the Cu6Sn5 Intermetallic

2021 ◽  
Author(s):  
A. Leineweber ◽  
M. Löffler ◽  
S. Martin
Keyword(s):  
Phase Equilibria ◽  
Electron Backscatter Diffraction ◽  
Metastable Phase ◽  
Stable Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Ordered Phases ◽  
Backscatter Diffraction ◽  
Kinetics Of

Abstract Cu6Sn5 intermetallic occurs in the form of differently ordered phases η, η′ and η′′. In solder joints, this intermetallic can undergo changes in composition and the state of order without or while interacting with excess Cu and excess Sn in the system, potentially giving rise to detrimental changes in the mechanical properties of the solder. In order to study such processes in fundamental detail and to get more detailed information about the metastable and stable phase equilibria, model alloys consisting of Cu3Sn + Cu6Sn5 as well as Cu6Sn5 + Sn-rich melt were heat treated. Powder x-ray diffraction and scanning electron microscopy supplemented by electron backscatter diffraction were used to investigate the structural and microstructural changes. It was shown that Sn-poor η can increase its Sn content by Cu3Sn precipitation at grain boundaries or by uptake of Sn from the Sn-rich melt. From the kinetics of the former process at 513 K and the grain size of the η phase, we obtained an interdiffusion coefficient in η of (3 ± 1) × 10−16 m2 s−1. Comparison of this value with literature data implies that this value reflects pure volume (inter)diffusion, while Cu6Sn5 growth at low temperature is typically strongly influenced by grain-boundary diffusion. These investigations also confirm that η′′ forming below a composition-dependent transus temperature gradually enriches in Sn content, confirming that Sn-poor η′′ is metastable against decomposition into Cu3Sn and more Sn-rich η or (at lower temperatures) η′. Graphic Abstract

scholarly journals Zeolite NaP1 Functionalization for the Sorption of Metal Complexes with Biodegradable N-(1,2-dicarboxyethyl)-D,L-aspartic Acid

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2518
Author(s):  
Dorota Kołodyńska ◽  
Yongming Ju ◽  
Małgorzata Franus ◽  
Wojciech Franus
Keyword(s):  
Experimental Data ◽  
Aspartic Acid ◽  
Ph Value ◽  
Complexing Agents ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
Modified Zeolite ◽  
X Ray ◽  
Slow Release Fertilizers ◽  
Pseudo Second Order

The possibility of application of chitosan-modified zeolite as sorbent for Cu(II), Zn(II), Mn(II), and Fe(III) ions and their mixtures in the presence of N-(1,2-dicarboxyethyl)-D,L-aspartic acid, IDHA) under different experimental conditions were investigated. Chitosan-modified zeolite belongs to the group of biodegradable complexing agents used in fertilizer production. NaP1CS as a carrier forms a barrier to the spontaneous release of the fertilizer into soil. The obtained materials were characterized by Fourier transform infrared spectroscopy (FTIR); surface area determination (ASAP); scanning electron microscopy (SEM-EDS); X-ray fluorescence (XRF); X-ray diffraction (XRD); and carbon, hydrogen, and nitrogen (CHN), as well as thermogravimetric (TGA) methods. The concentrations of Cu(II), Zn(II), Mn(II), and Fe(III) complexes with IDHA varied from 5–20 mg/dm3 for Cu(II), 10–40 mg/dm3 for Fe(III), 20–80 mg/dm3 for Mn(II), and 10–40 mg/dm3 for Zn(II), respectively; pH value (3–6), time (1–120 min), and temperature (293–333 K) on the sorption efficiency were tested. The Langmuir, Freundlich, Dubinin–Radushkevich, and Temkin adsorption models were applied to describe experimental data. The pH 5 proved to be appropriate for adsorption. The pseudo-second order and Langmuir models were consistent with the experimental data. The thermodynamic parameters indicate that adsorption is spontaneous and endothermic. The highest desorption percentage was achieved using the HCl solution, therefore, proving that method can be used to design slow-release fertilizers.

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