New Rapid Setting Alkali Activated Cement Compositions

1989 ◽  
Vol 179 ◽  
Author(s):  
D. M. Roy ◽  
M. R. Silsbee ◽  
D. Wolfe-Confer
Keyword(s):  
Mechanical Property ◽  
Alkali Activation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Blended Cements ◽  
Setting Times ◽  
Rapid Setting ◽  
Alkali Activated ◽  
Alkali Activated Cement

AbstractThe advantage of utilizing blended cements for many applications has been well documented. However, the use of these materials has been limited by the longer setting times associated with the use of these materials. This report discusses the development of formulations employing alkali activation to shorten the setting times. The results of characterization of these materials using calorimetry, microscopic, x-ray diffraction, and mechanical property techniques are discussed.

scholarly journals Zeolite Adsorption of Chloride from a Synthetic Alkali-Activated Cement Pore Solution

Materials ◽  
2019 ◽  
Vol 12 (12) ◽  
pp. 2019 ◽  
Author(s):  
Jorge Osio-Norgaard ◽  
Wil V. Srubar
Keyword(s):  
Chemical Composition ◽  
Pore Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Elemental Chlorine ◽  
Cage Size ◽  
Synthetic Zeolites ◽  
Diffraction Patterns ◽  
Alkali Activated ◽  
Alkali Activated Cement

This work presents experimental evidence that confirms the potential for two specific zeolites, namely chabazite and faujasite (with a cage size ~2–13 Å), to adsorb small amounts of chloride from a synthetic alkali-activated cement (AAC) pore solution. Four synthetic zeolites were first exposed to a chlorinated AAC pore solution, two faujasite zeolites (i.e., FAU, X-13), chabazite (i.e., SSZ-13), and sodium-stabilized mordenite (i.e., Na-Mordenite). The mineralogy and chemical composition were subsequently investigated via X-ray diffraction (XRD) and both energy- and wavelength-dispersive X-ray spectroscopy (WDS), respectively. Upon exposure to a chlorinated AAC pore solution, FAU and SSZ-13 displayed changes to their diffraction patterns (i.e., peak shifting and broadening), characteristic of ion entrapment within zeolitic aluminosilicate frameworks. Elemental mapping with WDS confirmed the presence of small amounts of elemental chlorine. Results indicate that the chloride-bearing capacity of zeolites is likely dependent on both microstructural features (e.g., cage sizes) and chemical composition.

Preparation and Characterization of PCL/PVP Blend Membrane

2011 ◽  
Vol 311-313 ◽  
pp. 1638-1641
Author(s):  
Jun Hua Wang ◽  
Xiang Biao Cheng ◽  
Gang Huang ◽  
Feng Chun Dong ◽  
Yong Tang Jia
Keyword(s):  
Mechanical Property ◽  
Membrane Structure ◽  
Solution Method ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Blend Membrane ◽  
X Ray ◽  
Structure And Morphology ◽  
Xrd Techniques

PCL/PVP blend membrane was prepared by casting solution method. Scanning electron microscopy (SEM), diffraction scanning calorimetry (DSC), and X-ray diffraction (XRD) techniques were employed to characterize membrane structure and morphology. Moreover, the hydrophilicity, mechanical property and biodegradability of membranes were investigated. Due to introducing PVP, the crystallinity and mechanical property of PCL altered to some extent. The hydrophilicity of the blend membrane improved remarkably with increasing PVP content, which was expressed by the contact angle declining and the rate of water absorption increasing. Lipase accelerated the degradation rate of PCL/PVP membrane.

scholarly journals Alkaline Activation of Kaolin Group Minerals

Crystals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 268 ◽  
Author(s):  
Oliwia Biel ◽  
Piotr Rożek ◽  
Paulina Florek ◽  
Włodzimierz Mozgawa ◽  
Magdalena Król
Keyword(s):  
Sodium Hydroxide ◽  
Water Glass ◽  
Small Addition ◽  
Alkali Activation ◽  
Structural Studies ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Bulk Materials ◽  
X Ray ◽  
Alkali Activated

Zeolites can be obtained in the process of the alkali-activation of aluminosilicate precursors. Such zeolite–geopolymer hybrid bulk materials merge the advantageous properties of both zeolites and geopolymers. In the present study, the effect of the type and concentration of an activator on the structure and properties of alkali-activated metakaolin, and metahalloysite was assessed. These two different kaolinite clays were obtained by the calcination of kaolin and halloysite, and then activated with sodium hydroxide and water glass. The phase compositions were assessed by X-ray diffraction, the microstructure was observed via scanning electron microscope, and the structural studies were conducted on the basis of the infrared spectra. The structure and properties of the obtained alkali-activated materials depend on both the type of a precursor and the type of an activator. The formation of zeolite phases was observed when the activation was carried out with sodium hydroxide alone, or with a small addition of water glass, regardless of the starting material used. The higher proportion of silicon in the activator solution does not give crystalline phases, but only an amorphous phase. Geopolymers based on metahalloysite have better compressive strength as the result of the better reactivity of metahalloysite compared to metakaolin.

scholarly journals The effect of the concentration of alkaline activator and aging time on the structure of metakaolin based geopolymer

2020 ◽  
Vol 52 (2) ◽  
pp. 219-229
Author(s):  
Marija Ivanovic ◽  
Ljiljana Kljajevic ◽  
Jelena Gulicovski ◽  
Marijana Petkovic ◽  
Ivona Jankovic-Castvan ◽  
...  
Keyword(s):  
Aging Time ◽  
Mass Spectra ◽  
Surface Characterization ◽  
Alkali Activation ◽  
X Ray Diffraction ◽  
Structural Reorganization ◽  
X Ray ◽  
Fourier Transformation Infrared Spectroscopy ◽  
Alkaline Activator

This paper outlines the production of an inorganic polymer/geopolymer using a metakaolin by an environmental friendly, energy saving, clean technology to conserve natural environment and resources. The influence of alkali activation, i.e. different concentration of NaOH as a component of alkali activator mixture on the process of geopolymerization of metakaolin is investigated. Also, process of aging time of geopolymer is followed by several analytical methods. The structure of metakaolin and metakaolin based geopolymers and their physicochemical properties were studied using X-ray diffraction (XRD), Fourier transformation infrared spectroscopy (FTIR) and after 28days scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) was applied for the surface characterization of the samples. A shift of the Si-O or Si-O-X (X=Al, Si, Na...) bands as the molarity of activator increasing during geopolymerization process was observed by FTIR. Mass spectra of geopolymers were characterized by MALDI TOF mass spectrometer. Structural reorganization of geopolymer samples occurs during the curing/aging in accordance with a geopolymerization mechanism.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

High Resolution Replication of Organoclay Surfaces

1982 ◽  
Vol 40 ◽  
pp. 576-577
Author(s):  
W. W. Barker ◽  
W. E. Rigsby ◽  
V. J. Hurst ◽  
W. J. Humphreys
Keyword(s):  
Clay Mineral ◽  
Organic Molecule ◽  
Organic Molecules ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Naturally Occurring ◽  
Silicate Layers ◽  
Mineral Identification

Experimental clay mineral-organic molecule complexes long have been known and some of them have been extensively studied by X-ray diffraction methods. The organic molecules are adsorbed onto the surfaces of the clay minerals, or intercalated between the silicate layers. Natural organo-clays also are widely recognized but generally have not been well characterized. Widely used techniques for clay mineral identification involve treatment of the sample with H2 O2 or other oxidant to destroy any associated organics. This generally simplifies and intensifies the XRD pattern of the clay residue, but helps little with the characterization of the original organoclay. Adequate techniques for the direct observation of synthetic and naturally occurring organoclays are yet to be developed.

Synthesis and characterization of TiN / Ti / AISI 410 coatings

2018 ◽  
Vol 2 (1) ◽  
pp. 7
Author(s):  
S Chirino ◽  
Jaime Diaz ◽  
N Monteblanco ◽  
E Valderrama
Keyword(s):  
Synthesis And Characterization ◽  
Photoemission Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Columnar Grains ◽  
Tin Thin Films ◽  
Steel Aisi ◽  
Interacting Surfaces ◽  
Stainless Steel Aisi

The synthesis and characterization of Ti and TiN thin films of different thicknesses was carried out on a martensitic stainless steel AISI 410 substrate used for tool manufacturing. The mechanical parameters between the interacting surfaces such as thickness, adhesion and hardness were measured. By means of the scanning electron microscope (SEM) the superficial morphology of the Ti/TiN interface was observed, finding that the growth was of columnar grains and by means of EDAX the existence of titanium was verified.  Using X-ray diffraction (XRD) it was possible to observe the presence of residual stresses (~ -3.1 GPa) due to the different crystalline phases in the coating. Under X-ray photoemission spectroscopy (XPS) it was possible to observe the molecular chemical composition of the coating surface, being Ti-N, Ti-N-O and Ti-O the predominant ones.

Studies on the Preparation, Characterization and Solubility of -Cyclodextrin-Roxythromycin Inclusion Complexes

2009 ◽  
Vol 2 (2) ◽  
pp. 523-530
Author(s):  
D. Nagasamy Venkatesh ◽  
S. Karthick ◽  
M. Umesh ◽  
G. Vivek ◽  
R.M. Valliappan ◽  
...  
Keyword(s):  
Dissolution Rate ◽  
Inclusion Complexes ◽  
Phase Solubility ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ir Studies ◽  
Poorly Soluble ◽  
Poorly Soluble Drug

Roxythromycin/ β-cyclodextrin (Roxy/ β-CD) dispersions were prepared with a view to study the influence of β-CD on the solubility and dissolution rate of this poorly soluble drug. Phase-solubility profile indicated that the solubility of roxythromycin was significantly increased in the presence of β-cyclodextrin and was classified as AL-type, indicating the 1:1 stoichiometric inclusion complexes. Physical characterization of the prepared systems was carried out by differential scanning calorimetry (DSC), X-ray diffraction studies (XRD) and IR studies. Solid state characterization of the drug β-CD binary system using XRD, FTIR and DSC revealed distinct loss of drug crystallinity in the formulation, ostensibly accounting for enhancement of dissolution rate.

New Coordination Compounds of Fe(III) with Organic Ligands

2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Mihaela Flondor ◽  
Ioan Rosca ◽  
Doina Sibiescu ◽  
Mihaela-Aurelia Vizitiu ◽  
Daniel-Mircea Sutiman ◽  
...  
Keyword(s):  
Chemical Analysis ◽  
Complex Compounds ◽  
Organic Ligands ◽  
X Ray Diffraction ◽  
X Ray ◽  
Elemental Chemical Analysis ◽  
Structural Formulae ◽  
Paramagnetic Properties

In this paper the synthesis and the study of some complex compounds of Fe(III) with ligands derived from: 2-(4-chloro-phenylsulfanyl)-1-(2-hydroxy-3,5-diiodo-phenyl)-ethanone (HL1), 1-(3,5-dibromo-2-hydroxy-phenyl)-2-phenylsulfanyl-ethanone(HL2), and 2-(4-chloro-phenylsulfanyl)-1-(3,5-dibromo-2-hydroxy-phenyl)-ethanone (HL3) is presented. The characterization of these complexes is based on method as: the elemental chemical analysis, IR and ESR spectroscopy, M�ssbauer, the thermogravimetric analysis and X-ray diffraction. Study of the IR and chemical analysis has evidenced that the precipitates form are a complexes and the combination ratio of M:L is 1:2. The central atoms of Fe(III) presented paramagnetic properties and a octaedric hybridization. Starting from this precipitation reactions, a method for the gravimetric determination of Fe(III) with this organic ligands has been possible. Based on the experimental data on literature indications, the structural formulae of the complex compounds are assigned.

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