scholarly journals Preparation of BaZrO3 powders by a spray-drying process

2003 ◽  
Vol 18 (6) ◽  
pp. 1325-1332 ◽  
Author(s):  
B. Robertz ◽  
F. Boschini ◽  
A. Rulmont ◽  
R. Cloots ◽  
I. Vandriessche ◽  
...  
Keyword(s):  
Spray Drying ◽  
Precursor Solution ◽  
Barium Zirconate ◽  
Drying Process ◽  
X Ray Diffraction ◽  
High Quality ◽  
Corrosion Resistant ◽  
X Ray ◽  
Potential Use ◽  
Scanning Electron

The potential use of barium zirconate for the manufacture of corrosion-resistant substrates emphasizes the need for a simple, inexpensive, and easily scalable process to produce high-quality powders with well-controlled composition and properties. However, the classical solid-state preparation of barium zirconate leads to an inhomogeneous powder unsuitable for applications in highly corrosive environment. For this paper, the possibility to use the spray-drying technique for the preparation of BaZrO3 powders with a controlled size distribution and morphology was investigated. The influence of the nature and concentration of the precursor solution and the influence of the spray-drying step are discussed on the basis of x-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and dilatometric measurements.

Corrosion Behavior of Q235A Steel under Wet-Dry Cyclic Condition

2012 ◽  
Vol 557-559 ◽  
pp. 139-142
Author(s):  
Jian Guo Liu ◽  
Yan Tao Li ◽  
Bao Rong Hou
Keyword(s):  
Electron Microscopy ◽  
Chloride Concentration ◽  
Corrosion Products ◽  
Drying Process ◽  
X Ray Diffraction ◽  
Cathodic Process ◽  
X Ray ◽  
Reduction Processes ◽  
Cyclic Condition ◽  
Scanning Electron

The corrosion processes and mechanisms of Q235A steel under wet-dry cyclic condition were studied using polarization curve compared with immersion samples, while, the corrosion morphologies and corrosion products of the steel samples were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD). The cathodic process of wet-dry samples was likely to be controlled not by the oxygen reduction, but rather by the reduction of corrosion products. During the drying process of the wet-dry sample, the electrolyte thickness decreased and chloride concentration increased. Oxygen would be much easier to diffuse into the interface of electrolyte/metal, which improved the cathodic reduction processes. Except for this, the rust itself took part in the reduction processes and hence increased the corrosion rate of the steel samples.

scholarly journals Layer-by-Layer Self-Assembled Ferrite Multilayer Nanofilms for Microwave Absorption

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Jiwoong Heo ◽  
Daheui Choi ◽  
Jinkee Hong
Keyword(s):  
Electron Microscopy ◽  
Self Assembly ◽  
Precursor Solution ◽  
Ferrite Nanoparticles ◽  
Energy Dispersive ◽  
Layer By Layer ◽  
X Ray Diffraction ◽  
Simple Method ◽  
X Ray ◽  
Scanning Electron

We demonstrate a simple method for fabricating multilayer thin films containing ferrite (Co0.5Zn0.5Fe2O4) nanoparticles, using layer-by-layer (LbL) self-assembly. These films have microwave absorbing properties for possible radar absorbing and stealth applications. To demonstrate incorporation of inorganic ferrite nanoparticles into an electrostatic-interaction-based LbL self-assembly, we fabricated two types of films: (1) a blended three-component LbL film consisting of a sequential poly(acrylic acid)/oleic acid-ferrite blend layer and a poly(allylamine hydrochloride) layer and (2) a tetralayer LbL film consisting of sequential poly(diallyldimethylammonium chloride), poly(sodium-4-sulfonate), bPEI-ferrite, and poly(sodium-4-sulfonate) layers. We compared surface morphologies, thicknesses, and packing density of the two types of ferrite multilayer film. Ferrite nanoparticles (Co0.5Zn0.5Fe2O4) were prepared via a coprecipitation method from an aqueous precursor solution. The structure and composition of the ferrite nanoparticles were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy, and scanning electron microscopy. X-ray diffraction patterns of ferrite nanoparticles indicated a cubic spinel structure, and energy dispersive X-ray spectroscopy revealed their composition. Thickness growth and surface morphology were measured using a profilometer, atomic force microscope, and scanning electron microscope.

scholarly journals Preparation and Properties of Ginger Essential Oil β-Cyclodextrin/Chitosan Inclusion Complexes

Coatings ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 305 ◽  
Author(s):  
Yan Zhang ◽  
Hui Zhang ◽  
Fang Wang ◽  
Li-Xia Wang
Keyword(s):  
Particle Size ◽  
Essential Oil ◽  
Spray Drying ◽  
Small Particle Size ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ft Ir ◽  
Thermal Stability Of ◽  
Scanning Electron

The ginger essential oil/β-cyclodextrin (GEO/β-CD) composite, ginger essential oil/β-cyclodextrin/chitosan (GEO/β-CD/CTS) particles and ginger essential oil/β-cyclodextrin/chitosan (GEO/β-CD/CTS) microsphere were prepared with the methods of inclusion, ionic gelation and spray drying. Their properties were studied by using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermo-gravimetry analysis (TGA), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). The results showed that the particle size of GEO/β-CD composite was smaller than that of β-CD and GEO/β-CD/CTS particles were loose and porous, while the microsphere obtained by spray drying had certain cohesiveness and small particle size. Besides, results also indicated that β-CD/CTS could modify properties and improve the thermal stability of GEO, which would improve its application value in food and medical industries.

Characterization of LSCF-Based Composite and LSCF as Cathodes for Intermediate Temperature SOFCs

2012 ◽  
Vol 727-728 ◽  
pp. 657-662
Author(s):  
Reinaldo Azevedo Vargas ◽  
Everton Bonturim ◽  
Marco Andreoli ◽  
Rubens Chiba ◽  
Emília Satoshi Miyamaru Seo
Keyword(s):  
Solid Oxide Fuel Cells ◽  
Solid Oxide ◽  
Intermediate Temperature ◽  
Oxide Fuel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Powder Spraying ◽  
Potential Use ◽  
Scanning Electron

The (La0.60Sr0.40)(Co0.20Fe0.80)O3-δ - LSCF, (Ce0.90Gd0.10)O1.95 - CGO composites and LSCF were deposited by wet powder spraying deposition method for the purpose of investigating their potential use in Intermediate Temperature Solid Oxide Fuel Cells. The interlayers are necessary between CGO electrolytes and LSCF cathodes in order to improve the performance of these materials. LSCF particles synthesized by citrate technique were calcined at 900 °C for 4 h and, their LSCF-CGO composites and LSCF suspensions deposited on CGO substrate and, sintered in 1100 °C for 1 h, were formed pseudo-perovskite. The ceramics materials were analyzed by X-ray diffraction (XRD) and chemical composition of different half-cells layers by scanning electron microscope with energy dispersive (SEM-EDS). The results are in agreement with the literature and indicate that route studied is adequate for crystal structures formation compatible with films the 35 µm thick total for study of conductivity between the cathode and the electrolyte.

Structural and Morphological Properties of HfxZr1-xO2 Thin Films Prepared by Pechini Route

2010 ◽  
Vol 644 ◽  
pp. 113-116
Author(s):  
L.A. García-Cerda ◽  
Bertha A. Puente Urbina ◽  
M.A. Quevedo-López ◽  
B.E. Gnade ◽  
Leo A. Baldenegro-Perez ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Annealing Temperature ◽  
Precursor Solution ◽  
Dip Coating ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dip Coating Technique ◽  
Scanning Electron

In this study, HfxZr1-xO2 (0 < x < 1) thin films were deposited on silicon wafers using a dip-coating technique and by using a precursor solution prepared by the Pechini route. The effects of annealing temperature on the structure and morphological properties of the proposed films were investigated. HfxZr1-xO2 thin films with 1, 3 and 5 layers were annealed in air for 2 h at 600 and 800 °C and the structural and morphological properties studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM). XRD results show that the films have monoclinic and tetragonal structure depending of the Hf and Zr concentration. SEM photographs show that all films consist of nanocrystalline grains with sizes in the range of 6 - 13 nm. The total film thickness is about 90 nm.

Study of Fluxing Process for Hot Dipping Galfan Alloy on Steel Wire

2011 ◽  
Vol 383-390 ◽  
pp. 1901-1904
Author(s):  
An Du ◽  
Yan Huo ◽  
Jie Hu
Keyword(s):  
Orthogonal Experiment ◽  
Steel Wire ◽  
Optimal Parameters ◽  
X Ray Diffraction ◽  
Experiment Research ◽  
Corrosion Resistant ◽  
X Ray ◽  
Corrosion Resistant Coatings ◽  
Fluxing Agent ◽  
Scanning Electron

Through the orthogonal experiment, research on the process parameters of the qualiity coating with the new auxiliary ,such as different pickled time, parched time, hot-dip time , and analyzed by scanning electron microscopy, X-ray diffraction. The results show that BiOCl is a new fluxing agent and the optimal parameters for pickled time, the parch time , hot-dip time, respectively,10s,120s,9s,through this we can get bright, smooth, corrosion resistant coatings.

scholarly journals Effect of H2O Activity on Zeolite Formation

Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4780
Author(s):  
Claudia Belviso ◽  
Francesco Cavalcante
Keyword(s):  
Liquid Nitrogen ◽  
Sodium Aluminate ◽  
Drying Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lta Zeolite ◽  
Zeolite Formation ◽  
Silica Alumina ◽  
Over Time ◽  
Scanning Electron

In an effort to understand the effects of H2O activity on zeolite formation, we have synthesized LTA zeolite using a combination of freezing processes and varying drying temperatures. Sodium aluminate and sodium silicate were used to form LTA zeolite, according to the IZA (International Zeolite Association) protocol. The synthesis steps were modified by adding the precursor frozen process by a rapid liquid nitrogen (−196 °C) treatment or slow conventional freezer treatment (−20 °C). The samples were subsequently sonicated and then dried at 80 °C or 40 °C. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were performed on the samples immediately after the drying process as well as after 2 weeks and 1 month of aging the solid products. The results indicated that LTA zeolite does not form. The silica-alumina precursor after both freezing processes and after being dried at 80 °C showed the presence of sodalite displaying stable behavior over time. Both sets of samples dried at 40 °C and did not show the presence of zeolite immediately after the drying process. However, after 2 weeks, the liquid nitrogen–frozen precursor was characterized by the presence of EMT whereas zeolites never formed in the −20 °C samples. These results suggest that freezing processes differently control the H2O activity during the drying and aging processes in the solid state. Thus, although the precursor chemical composition is the same, the type of zeolite formed is different.

scholarly journals Influence of Strong Acid Hydrolysis Processing on the Thermal Stability and Crystallinity of Cellulose Isolated from Wheat Straw

2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
Chemar J. Huntley ◽  
Kristy D. Crews ◽  
Mohamed A. Abdalla ◽  
Albert E. Russell ◽  
Michael L. Curry
Keyword(s):  
Electron Microscopy ◽  
Thermal Stability ◽  
Scanning Electron Microscopy ◽  
Acid Hydrolysis ◽  
Wheat Straw ◽  
Cellulose Fibers ◽  
Drying Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Cellulose extractions from wheat straw via hydrochloric, nitric, and sulfuric acid hydrolysis methods were carried out. X-ray diffraction spectral analyses reveal that depending on the acid conditions used the structure of the cellulose exhibited a mixture of polymorphs (i.e., CI and CIII cellulose phases). In addition, the percent crystallinity, diameter, and length of the cellulose fibers varied tremendously as determined by X-ray diffraction and scanning electron microscopy. Thermal gravimetric analysis measurements revealed that the thermal stability of the extracted cellulose varied as a function of the acid strength and conditions used. Scanning electron microscopy analysis revealed that the aggregation of cellulose fibers during the drying process is strongly dependent upon the drying process and strength of the acids used.

scholarly journals Nano-CL-20/HMX Cocrystal Explosive for Significantly Reduced Mechanical Sensitivity

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Chongwei An ◽  
Hequn Li ◽  
Baoyun Ye ◽  
Jingyu Wang
Keyword(s):  
Spray Drying ◽  
Raw Materials ◽  
Drop Height ◽  
Drying Method ◽  
X Ray Diffraction ◽  
Mechanical Sensitivity ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Friction Sensitivity ◽  
Scanning Electron

Spray drying method was used to prepare cocrystals of hexanitrohexaazaisowurtzitane (CL-20) and cyclotetramethylene tetranitramine (HMX). Raw materials and cocrystals were characterized using scanning electron microscopy, X-ray diffraction, differential scanning calorimetry, Raman spectroscopy, and Fourier transform infrared spectroscopy. Impact and friction sensitivity of cocrystals were tested and analyzed. Results show that, after preparation by spray drying method, microparticles were spherical in shape and 0.5–5 µm in size. Particles formed aggregates of numerous tiny plate-like cocrystals, whereas CL-20/HMX cocrystals had thicknesses of below 100 nm. Cocrystals were formed by C–H⋯O bonding between –NO2 (CL-20) and –CH2– (HMX). Nanococrystal explosives exhibited drop height of 47.3 cm, and friction demonstrated explosion probability of 64%. Compared with raw HMX, cocrystals displayed significantly reduced mechanical sensitivity.

scholarly journals ZnO Film Photocatalysts

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Bosi Yin ◽  
Siwen Zhang ◽  
Dawei Zhang ◽  
Yang Jiao ◽  
Yang Liu ◽  
...  
Keyword(s):  
Waste Water ◽  
Zno Films ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
Zno Film ◽  
High Quality ◽  
X Ray ◽  
Photodegradation Efficiency ◽  
Hydrothermal Approach ◽  
Scanning Electron

We have synthesized high-quality, nanoscale ultrathin ZnO films at relatively low temperature using a facile and effective hydrothermal approach. ZnO films were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), Raman spectroscopy, photoluminescence spectra (PL), and UV-vis absorption spectroscopy. The products demonstrated 95% photodegradation efficiency with Congo red (CR) after 40 min irradiation. The photocatalytic degradation experiments of methyl orange (MO) and eosin red also were carried out. The results indicate that the as-obtained ZnO films might be promising candidates as the excellent photocatalysts for elimination of waste water.

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