The Chemistry of Al-Tobermorite and its Coexisting Phases AT 175°C

1989 ◽  
Vol 179 ◽  
Author(s):  
Mary W. Barnes ◽  
Barry E. Scheetz

AbstractThe substitution of Al into the structure of tobermorite was investigated, along with the resultant phase assemblages that compatibly coexist with the Al-tobermorite. All experiments were conducted under hydrothermal conditions at saturated steam pressure. The temperatures of the experiments varied from 90° to 190°C and times from 1 to 28 days. Ca/Si ratios varied from 0.7 to 1.7, Al/(Al+Si) from 0.12 to 0.30. NaOH varied from none to 5 moles/mole tobermorite constituents. X-ray diffraction was used not only to identify phases but to determine degree of substitution and the rate of approach to steady state.Maximum Al substitution was found to be Al/(Al+Si) = 0.13, and the maximum interlayer spacing was 11.42 ± 0.015 Å. This is in agreement with previously published work which found a trace of hydrogarnet at Al(Al+Si) = 0.15 and a maximum interlayer spacing of 11.45 ± 0.02 A. When Al concentrations in the mix are greater than enough to make maximum Al-tobermorite, “low”-hydrogarnet (“low”-hydrogarnet has ∼0.1 SiO2 per mole). As Al concentration is raised, a variable composition hydrogamet is formed and then a “high”-garnet of constant composition (SiO2 = 0.7 moles/mole hydrogarnet) is formed.NaOH was found to have a major effect on the kinetics and the phase assemblages at a given time. Al-tobermorite, although stable at 90°C, converts to xonotlite at 175°C in the absence of NaOH. In its presence, even at a level too low to make Na-containing phases, Al-tobermorite persists at 21 days at 175°C. In the absence of NaOH, at 175°C, Al-tobermorite forms at up to 7–10 days but is converted to xonotlite at 28 days. Coexisting phases are gyrolite and cowlesite at Ca/Si ≥ 1 and hillebrandite and “low”-garnet at Ca/Si > 1. When there is enough NaOH to form Na-containing phases, Al-tobermorite coexists with reyerite and analcime at Ca/Si > 1. At Ca/Si < 1 and Al less than the composition on the tie line between Al-tobermorite and “low”-garnet, Al-tobermorite coexists with “low”-garnet and portlandite. In the compatibility triangle between Al-tobermorite, “low”-garnet, and “high”-garnet, Al-tobermorite coexists with variable Si-gamet. When Al exceeds its limiting value on the tie line, Al-tobermorite-“high”-gamet, the assemblage is Al-tobermorite-“high”-gamet-cowlesite.

2012 ◽  
Vol 204-208 ◽  
pp. 3644-3647
Author(s):  
Chang Jun Ke ◽  
Shu Ying Wang ◽  
Jun Li Liu

the relationship between hydration products transformation and the compressive strength was studied with X-ray diffraction, infrared spectroscopy analysis. The results showed, 0.505nm hydrogarnets diffraction peaks weakened and 0.183nm CSH diffraction peak enhanced with different autoclaved time under 1.2MPa saturated steam pressure. 0.505nm hydrogarnets diffraction peak enhanced under lower saturated steam pressure for autoclaving 6h, then weaken under higher saturated steam pressure. And 0.183nm CSH diffraction peaks enhanced with different saturated steam pressure for autoclaving 6h. During autoclaving, hydrogarnet translate into Al-substituted calcium silicate hydrate (C-S-H). Transformation of hydration products is favorable for compressive strength of autoclaved sample.


2015 ◽  
Vol 71 (4) ◽  
pp. 330-337 ◽  
Author(s):  
Sabina Kovač ◽  
Ljiljana Karanović ◽  
Tamara Đorđević

Two isostructural diarsenates, SrZnAs2O7(strontium zinc diarsenate), (I), and BaCuAs2O7[barium copper(II) diarsenate], (II), have been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The three-dimensional open-framework crystal structure consists of corner-sharingM2O5(M2 = Zn or Cu) square pyramids and diarsenate (As2O7) groups. Each As2O7group shares its five corners with five differentM2O5square pyramids. The resulting framework delimits two types of tunnels aligned parallel to the [010] and [100] directions where the large divalent nine-coordinatedM1 (M1 = Sr or Ba) cations are located. The geometrical characteristics of theM1O9,M2O5and As2O7groups of known isostructural diarsenates, adopting the general formulaM1IIM2IIAs2O7(M1II= Sr, Ba, Pb;M2II= Mg, Co, Cu, Zn) and crystallizing in the space groupP21/n, are presented and discussed.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Xinzhao Xia ◽  
Lixian Xia ◽  
Geng Zhang ◽  
Yuxuan Jiang ◽  
Fugang Sun ◽  
...  

Abstract In this work, a new type of zinc(II) coordination polymer {[Zn(HIDC)(BBM)0.5]·H2O} n (Zn-CP) was synthesized using 4,5-imidazoledicarboxylic acid (H3IDC) and 2,2-(1,4-butanediyl)bis-1,3-benzimidazole (BBM) under hydrothermal conditions. Its structure has been characterized by infrared spectroscopy, elemental analysis and single crystal X-ray diffraction analysis. The Zn(II) ion is linked by the HIDC2− ligand to form a zigzag chain by chelating and bridging, and then linked by BBM to form a layered network structure. Adjacent layers are further connected by hydrogen bond interaction to form a 3-D supramolecular framework. The solid-state fluorescence performance of Zn-CP shows that compared with free H3IDC ligand, its fluorescence intensity is significantly enhanced.


2014 ◽  
Vol 68 (8) ◽  
Author(s):  
Selvakumar Dhanasingh ◽  
Dharmaraj Nallasamy ◽  
Saravanan Padmanapan ◽  
Vinod Padaki

AbstractThe influence of cetyltrimethylammonium bromide and ethylene glycol on the size and dispersion of indium oxide nanoparticles prepared under hydrothermal conditions was investigated. The precursor compound, indium hydroxide, obtained by the hydrothermal method in the absence as well as the presence of cetyltrimethylammonium bromide, was converted to indium oxide by sintering at 400°C. The formation of nanoscale indium oxide upon sintering was ascertained by the characteristic infrared adsorption bands and X-ray diffraction patterns of indium oxide. Transmission electron microscopy and band gap values confirmed that the cetyltrimethylammonium bromide facilitated the formation of indium oxide nanoparticles smaller in size and narrower in distribution than those prepared without the assistance of cetyltrimethylammonium bromide.


Polymers ◽  
2018 ◽  
Vol 10 (8) ◽  
pp. 896 ◽  
Author(s):  
Qiqi Fan ◽  
Guangping Han ◽  
Wanli Cheng ◽  
Huafeng Tian ◽  
Dong Wang ◽  
...  

In this work, an easy way to prepare the polylactic acid (PLA)/wheat straw fiber (WSF) composite was proposed. The method involved uses either the dopamine-treated WSF or the two-step montmorillonite (MMT)-modified WSF as the filler material. In order to achieve the dispersibility and exfoliation of MMT, it was modified by 12-aminododecanoic acid using a two-step route. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were performed to characterize the modified MMT and the coated WSF. As for the properties of PLA/WSF composites, some thermal (using Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis) and mechanical properties (flexural, tensile, and impact) were analyzed. The results showed that the dopamine was successfully coated onto the WSF. Furthermore, Na-MMT was successfully transformed to organo-montmorillonite (OMMT) and formed an exfoliated structure. In addition, a better dispersion of MMT was obtained using the two-step treatment. The interlayer spacing of modified MMT was 4.06 nm, which was 123% higher than that of the unmodified MMT. Additionally, FT-IR analysis suggested that OMMT diffused into the PLA matrix. The thermogravimetric analysis (TGA) showed that a higher thermal stability of PLA/WSF composites was obtained for the modified MMT and dopamine. The results also showed that both the dopamine treated WSF and the two-step-treated MMT exhibited a positive influence on the mechanical properties of PLA/WSF composites, especially on the tensile strength, which increased by 367% compared to the unmodified precursors. This route offers researchers a potential scheme to improve the thermal and mechanical properties of PLA/WSF composites in a low-cost way.


2019 ◽  
Vol 95 (7) ◽  
pp. 614-617 ◽  
Author(s):  
Alisa V. Balakayeva ◽  
N. V. Rusakov

There are presented results of the comparative evaluation of the effectiveness of plants for disinfection of medical waste which use 4 most common hardware technologies: treatment by saturated steam pressure, moist heat, microwave exposure and chemical disinfection with refinement. The efficiency ofplants using physical methods of influence was shown to be higher in comparison with hardware chemical disinfection.


2011 ◽  
Vol 396-398 ◽  
pp. 417-420 ◽  
Author(s):  
Xiao Hua Gu ◽  
Shi Wei Li ◽  
Bing Zheng ◽  
Jia Liang Zhou

A novel method is proposed to modify montmorillonite with anionic surfactants, cationic surfactants and halides stearyl cationic surfactants made by our group (Z-surfactant). The structure of organophilic montmorillonite (OMMT) was characterized by XRD and TG. The results of X-ray diffraction show that cationic surfactants and anionic surfactants are all intercalated into the layer of MMT. When modified with cationic surfactants, the interlayer spacing of MMT increases from 1.24 nm to the maximum of 3.76 nm. When it was secondary modified, the insertion order is to insert the cation first and then the anion. The interlayer spacing of montmorillonite increases to 4.80 nm, the modification effect is well.


2016 ◽  
Vol 694 ◽  
pp. 88-93
Author(s):  
Ahmad Fauzi Mohd Noor ◽  
Harmiza Zainudin

Sintering has major effect on the final properties of materials such as density, porosity and microstructure. Sintering of Mg-Si CHA in particular is a complex process since changes could occur during sintering, which include phase formation, grain size, pore size and carbonate content, and this in turn affects the mechanical properties. Improved mechanical properties of Mg-Si CHA is critical in load bearing implant applications. Poor control of thermal treatment of Mg-Si CHA during sintering would cause carbonate loss, leading to partial or total decomposition of Mg-Si CHA, subsequently would affect the physical and mechanical properties. The influence of powder properties (particle size, porosity, morphology) and sintering parameters (heating rate, firing atmosphere) on the sintered Mg-Si CHA microstructure was studied using scanning electron microscopy (SEM) characterization technique. The SEM results showed that we are able to produce sintered Mg-Si CHA without cracking of the compacted pellets, while keeping the carbonate level in the amount required (2 – 8%). X-Ray diffraction (XRD) was also performed on the sintered samples and the results indicated that a single phase Mg-Si-CHA was obtained, while Fourier transform infra-red (FTIR) spectroscopy result confirmed that as-synthesized Mg-Si CHA powder was a B-type.


2018 ◽  
Vol 74 (8) ◽  
pp. 936-943
Author(s):  
Galina V. Kiriukhina ◽  
Olga V. Yakubovich ◽  
Ekaterina M. Kochetkova ◽  
Olga V. Dimitrova ◽  
Anatoliy S. Volkov

Caesium manganese hexahydrate phosphate, CsMn(H2O)6(PO4), was synthesized under hydrothermal conditions. Its crystal structure was determined from single-crystal X-ray diffraction data. The novel phase crystallizes in the hexagonal space group P63 mc and represents the first manganese member in the struvite morphotropic series, AM(H2O)6(TO4). Its crystal structure is built from Mn(H2O)6 octahedra and PO4 tetrahedra linked into a framework via hydrogen bonding. The large Cs atoms are encapsulated in the framework cuboctahedral cavities. It is shown that the size of the A + ionic radius within the morphotropic series AM(H2O)6(XO4) results is certain types of crystal structures and affects the values of the unit-cell parameters. Structural relationships with Na(H2O)Mg(H2O)6(PO4) and the mineral hazenite, KNa(H2O)2Mg2(H2O)12(PO4)2, are discussed.


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