scholarly journals Use of Steel Industry Wastes for the Preparation of Self-Cleaning Mortars

Materials ◽  
2019 ◽  
Vol 12 (4) ◽  
pp. 621 ◽  
Author(s):  
José Balbuena ◽  
Luis Sánchez ◽  
Manuel Cruz-Yusta
Keyword(s):  
Steel Industry ◽  
Diffuse Reflectance ◽  
Construction Material ◽  
Added Value ◽  
X Ray Diffraction ◽  
X Ray ◽  
Before And After ◽  
New Material ◽  
Lamination Process ◽  
Self Cleaning

An important problem, which must be solved, is the accumulation of industrial waste in landfills. Science has an obligation to transform this waste into new products and, if possible, with high added value. In this sense, we propose the valorization of the waste which is generated in the steel lamination process (HSL) through its conversion into a new material with photocatalytic activity which is suitable for use as an additive to obtain a self-cleaning construction material. The valorization of steel husk lamination waste is achieved through a grinding process, which allows the sample to be homogenized, in size, without altering its phase composition, and a thermal treatment that turns it into iron oxide, which acts as a photocatalyst. These residues, before and after treatment, were characterized by different techniques such as PXRD (Powder X-Ray Diffraction), TGA (Thermogravimetric Analysis), SBET (Specific surface area, Brunauer-Emmett-Teller), SEM (Scanning Electron Microscopy) and Diffuse reflectance (DR). MB and RhB tests show that this material is capable of self-cleaning, both of the material itself and when it is incorporated into a construction material (mortar). In addition, the NOx gas elimination test shows that it is also capable of acting on greenhouse gases such as NOx.

Evaluation of the Apatite Coating on Silicon Nitride Based Ceramics Sintered with Re2O3 Additives (Re = Y, La, Yb)

2012 ◽  
Vol 727-728 ◽  
pp. 1243-1248
Author(s):  
Juliana Marchi ◽  
Cecília Chaves Guedes e Silva ◽  
E.C.S. Rigo ◽  
Ana Helena de Almeida Bressiani ◽  
José Carlos Bressiani
Keyword(s):  
Silicon Nitride ◽  
Diffuse Reflectance ◽  
X Ray Diffraction ◽  
Promising Candidate ◽  
X Ray ◽  
Apatite Coating ◽  
Biomimetic Coating ◽  
Before And After ◽  
Diffuse Reflectance Infrared ◽  
Zirconia Implants

As alternative for alumina and zirconia implants, silicon nitride based ceramics are considered promising candidate due to its biocompatibility and mechanical properties. However, this materials exhibit a bioinert character, leading to clinical failures. To overcome this problem, a biomimetic coating of hydroxyapatite is proposed in this paper, so that the surface can be bioactive and, consequently, the osteointegration process can be enhanced. Silicon nitride samples were sintered with different additives (Y, La and Yb) and the surfaces before and after coating were characterized by diffuse reflectance infrared Fourier transformed (DRIFT), X ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed that the surfaces of bioinert silicon nitride samples sintered with different additives could be transformed into bioactive by the formation of a hydroxyapatite layer through biomimetic process.

Evaluation of Freezing Methods by Low Temperature X-Ray Diffraction

1977 ◽  
Vol 35 ◽  
pp. 330-333
Author(s):  
T. Gulik-Krzywicki ◽  
M.J. Costello
Keyword(s):  
Biological Materials ◽  
Molecular Organization ◽  
X Ray Diffraction ◽  
Glass Capillary ◽  
X Ray ◽  
Rate Dependent ◽  
Before And After ◽  
Freeze Etching ◽  
Diffraction Patterns ◽  
Set Up

Freeze-etching electron microscopy is currently one of the best methods for studying molecular organization of biological materials. Its application, however, is still limited by our imprecise knowledge about the perturbations of the original organization which may occur during quenching and fracturing of the samples and during the replication of fractured surfaces. Although it is well known that the preservation of the molecular organization of biological materials is critically dependent on the rate of freezing of the samples, little information is presently available concerning the nature and the extent of freezing-rate dependent perturbations of the original organizations. In order to obtain this information, we have developed a method based on the comparison of x-ray diffraction patterns of samples before and after freezing, prior to fracturing and replication.Our experimental set-up is shown in Fig. 1. The sample to be quenched is placed on its holder which is then mounted on a small metal holder (O) fixed on a glass capillary (p), whose position is controlled by a micromanipulator.

A New Polyethylene Corrosion Protecting Coating with Ion Selectivity

2011 ◽  
Vol 314-316 ◽  
pp. 273-278
Author(s):  
Yu Hua Dong ◽  
Ke Ren ◽  
Qiong Zhou
Keyword(s):  
Ion Selectivity ◽  
Nano Particles ◽  
Ammonium Bromide ◽  
Linear Low Density Polyethylene ◽  
X Ray Diffraction ◽  
Sulfosalicylic Acid ◽  
X Ray ◽  
Chemically Modified ◽  
Before And After ◽  
Industrial Standards

Linear low density polyethylene (LLDPE) was chemically modified with grafting maleic anhydride (MAH) monomer on its backbone by melting blending. Nano-particles SiO2 was modified by cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB) and anionic surfactant sulfosalicylic acid (SSA) and added to PE coating respectively. Measurement of membrane potential showed that the coating containing modified SiO2 nano-particles had characteristic of ion selectivity. The properties of the different coatings were investigated according to relative industrial standards. Experimental results indicated that PE coating with ion selectivity had better performances, such as adhesion strength, cathodic disbonding and anti-corrosion, than those of coating without ion selectivity. Crystal structure of the coatings before and after alkali corrosion was characterized by Fourier transform infrared spectra (FTIR) and X-ray diffraction (XRD). Structure of the coating without ion selectivity was damaged by NaOH alkali solution, causing mechanical properties being decreased. And the structure of the ion selective coatings was not affected.

Sedimentary Clays as Geopolymer Precursor

2018 ◽  
Vol 39 ◽  
pp. 97-111
Author(s):  
F. Mostefa ◽  
Nasr Eddine Bouhamou ◽  
H.A. Mesbah ◽  
Salima Aggoun ◽  
D. Mekhatria
Keyword(s):  
Sodium Hydroxide ◽  
Mineralogical Composition ◽  
Cementitious Materials ◽  
Raw Material ◽  
X Ray Diffraction ◽  
Calcination Time ◽  
Calorimetric Analysis ◽  
X Ray ◽  
Before And After ◽  
Mechanical Performances

This work aims to study the feasibility of making a geopolymer cement based on dredged sediments, from the Fergoug dam (Algeria) and to evaluate their construction potential particularly interesting in the field of special cementitious materials. These sediments due to their mineralogical composition as aluminosilicates; are materials that can be used after heat treatment. Sedimentary clays were characterized before and after calcination by X-ray diffraction, ATG / ATD, spectroscopy (FTIR) and XRF analysis. The calcination was carried out on the raw material sieved at 80 μm for a temperature of 750 ° C, for 3.4 and 5 hours. The reactivity of the calcined products was measured using isothermal calorimetric analysis (DSC) on pastes prepared by mixing an alkaline solution of sodium hydroxide (NaOH) 8 M in an amount allowing to have a Na / Al ratio close to 1 (1: 1). Also, cubic mortar samples were prepared with a ratio L / S: 0.8, sealed and cured for 24 hours at 60 ° C and then at room temperature until the day they were submited to mechanical testing. to check the extent of geopolymerization. The results obtained allowed to optimize the calcination time of 5 hours for a better reactivity of these sediments, and a concentration of 8M of sodium hydroxide and more suitable to have the best mechanical performances.

Full-field X-ray diffraction microscopy using polymeric compound refractive lenses

2014 ◽  
Vol 47 (6) ◽  
pp. 1882-1888 ◽  
Author(s):  
J. Hilhorst ◽  
F. Marschall ◽  
T. N. Tran Thi ◽  
A. Last ◽  
T. U. Schülli
Keyword(s):  
Imaging Techniques ◽  
Light And Electron Microscopy ◽  
Added Value ◽  
Acquisition Time ◽  
Imaging Method ◽  
X Ray Diffraction ◽  
Polymeric Compound ◽  
Full Field ◽  
X Ray ◽  
Diffraction Imaging

Diffraction imaging is the science of imaging samples under diffraction conditions. Diffraction imaging techniques are well established in visible light and electron microscopy, and have also been widely employed in X-ray science in the form of X-ray topography. Over the past two decades, interest in X-ray diffraction imaging has taken flight and resulted in a wide variety of methods. This article discusses a new full-field imaging method, which uses polymer compound refractive lenses as a microscope objective to capture a diffracted X-ray beam coming from a large illuminated area on a sample. This produces an image of the diffracting parts of the sample on a camera. It is shown that this technique has added value in the field, owing to its high imaging speed, while being competitive in resolution and level of detail of obtained information. Using a model sample, it is shown that lattice tilts and strain in single crystals can be resolved simultaneously down to 10−3° and Δa/a= 10−5, respectively, with submicrometre resolution over an area of 100 × 100 µm and a total image acquisition time of less than 60 s.

Visible-Light-Induced Photocatalytic Activity of Boron-Doped BiVO4

2014 ◽  
Vol 809-810 ◽  
pp. 890-894
Author(s):  
Dan Li ◽  
Lian Wei Shan ◽  
Gui Lin Wang ◽  
Li Min Dong ◽  
Wei Li ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Diffuse Reflectance ◽  
Diffuse Reflectance Spectroscopy ◽  
Sol Gel ◽  
Reflectance Spectroscopy ◽  
Scheelite Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Boron Doped

Boron-BiVO4 samples were synthesized by sol-gel method. They were characterized by UV-vis diffuse reflectance spectroscopy, X-ray diffraction. Photocatalytic activity of the obtained BiVO4 samples was investigated through degrading methylene blue (MB). The results reveal that boron-BiVO4 catalysts have monoclinic scheelite structure. The BiVO4 and Co-BiVO4 photocatalysts were responsive to visible light. Co-BiVO4 photocatalyst showed higher photocatalytic activity than pure BiVO4, resulting in the significantly improved efficiency of degradation of MB.

Aging of iron manganite negative temperature coefficient thermistors

1998 ◽  
Vol 13 (5) ◽  
pp. 1238-1242 ◽  
Author(s):  
T. Battault ◽  
R. Legros ◽  
A. Rousset
Keyword(s):  
Temperature Coefficient ◽  
Spinel Structure ◽  
Negative Temperature Coefficient ◽  
Negative Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Octahedral Sites ◽  
Before And After ◽  
Structural Equilibrium ◽  
Electrical Data

“Aging,” defined as the drift of resistance with temperature after 1000 h, was investigated for iron manganite temperature coefficient thermistors. For these devices, aging is relatively large, about 10%. The cationic distributions before and after aging were determined by Mössbauer spectroscopy. These distributions explain all the x-ray diffraction and correlated electrical data. The origin of the aging observed on iron manganites thermistors has been identified. It is due to the migration of Fe3+ ions from tetrahedral to octahedral sites of the spinel structure in order to reach a structural equilibrium.

scholarly journals Carbonation Resistance of Surface Protective Materials Modified with Hybrid NanoSiO2

Coatings ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 269
Author(s):  
Kailun Xia ◽  
Yue Gu ◽  
Linhua Jiang ◽  
Mingzhi Guo ◽  
Lei Chen ◽  
...  
Keyword(s):  
Construction Material ◽  
Chemical Components ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Carbonation Depth ◽  
X Ray ◽  
Carbonation Resistance ◽  
Ideal Situation ◽  
Caco3 Content ◽  
Reference Samples

To date, reinforcement concrete is the main construction material worldwide. As the concentration of atmospheric CO2 is steadily increasing, carbonation of the reinforcement concrete becomes a pressing concern. In this study, novel surface protective materials (SPMs) modified with hybrid nanoSiO2 (HNS), fly ash, and slag were developed to reduce CO2 emissions and extend the service life of the reinforcement concrete. The carbonation depths were measured by phenolphthalein to reflect the carbonation resistance. X-ray diffraction (XRD), fourier-transform infrared spectroscopy (FTIR), and thermal gravimetric analysis (TGA) were conducted to analyze the chemical components of the samples after carbonation. In addition, MIP was carried out to examine the microstructures of the samples prior to carbonation. Thermodynamic modeling was employed to calculate the changes in the phase assemblages of each blends in an ideal situation. The experimental results showed that the carbonation depth and CaCO3 content of the SPM modified with HNS decreased by 79.0% and 64.6% compared with the reference, respectively. The TGA results showed that after carbonation, the CaCO3 contents were 4.40% and 12.42% in the HNS modified samples and reference samples, respectively. MIP analysis demonstrated that the incorporation of HNS in SPM led to a 48.3% and 58.5% decrease in big pores and capillary pores, respectively. Overall, the SPMs modified with HNS in this study possessed better carbonation resistance and refined pore structures.

Oxidation of Alloy-X in Subcritical, Transition, and Supercritical Water

CORROSION ◽  
10.5006/3881 ◽  
2021 ◽  
Author(s):  
Zachary Karmiol ◽  
Dev Chidambaram
Keyword(s):  
Supercritical Water ◽  
Photoelectron Spectroscopy ◽  
Focused Ion Beam ◽  
Elevated Temperatures ◽  
Subcritical Water ◽  
Ion Beam ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nickel Based Superalloy ◽  
Before And After

This work investigates the oxidation of a nickel based superalloy, namely Alloy X, in water at elevated temperatures: subcritical water at 261°C and 27 MPa, the transition between subcritical and supercritical water at 374°C and 27 MPa, and supercritical water at 380°C and 27 MPa for 100 hours. The morphology of the sample surfaces were studied using scanning electron microscopy coupled with focused ion beam milling, and the surface chemistry was investigated using X-ray diffraction, Raman spectroscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy before and after exposure studies. Surfaces of all samples were identified to comprise of a ferrite spinel containing aluminum.

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