Preparation and Characterization of A Composite Obtained through Ti (IV) and Phosphoric Acid

2014 ◽  
Vol 775-776 ◽  
pp. 97-101
Author(s):  
Loanda Raquel Cumba ◽  
U.O. Bicalho ◽  
D.R. Carmo
Keyword(s):  
Phosphoric Acid ◽  
Titanium Isopropoxide ◽  
Deionized Water ◽  
Spherical Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electron Microscopies ◽  
Prepared Material ◽  
Scanning Electron

This paper describes the preparation and complementary characterization of a composite formed from the activation of titanium isopropoxide by phosphoric acid and deionized water (TiP).Techniques such as, X-ray diffraction (XRD), Raman , electronic (UV-vis) and Scanning electron microscopies (SEM) were used for characterization of this new composite formed. In the X-ray diffractogram of TIP was observed four intense peaks. A strong absorption was observed in the region 362-445 nm. The scanning electron microscopy of TiP, shows that the prepared material consists mostly of a cluster of spherical particles with diameters ranging from 2.35 to 2.60 μm.

Synthesis and characterization of polyether structure carbon nitride

2004 ◽  
Vol 19 (6) ◽  
pp. 1736-1741 ◽  
Author(s):  
Tiancheng Mu ◽  
Jun Huang ◽  
Zhimin Liu ◽  
Buxing Han ◽  
Zhonghao Li ◽  
...  
Keyword(s):  
Spectroscopic Data ◽  
Carbon Nitride ◽  
Average Diameter ◽  
Building Blocks ◽  
Spherical Particles ◽  
X Ray Diffraction ◽  
Substantial Evidence ◽  
X Ray ◽  
Prepared Material

Carbon nitride powder with an atomic N/C ratio of 1 has been prepared by reaction of cyanuric chloride with sodium metal. X-ray diffraction, Fourier transform infrared spectra, and x-ray photoelectron spectroscopic data provide substantial evidence for a graphite-like sp2-bonded structure composed of building blocks of s-triazine rings bridged by carbon-carbon atoms in the bulk carbon nitride. The electron-microscopy results reveal that the material is spherical particles with an average diameter of 50 nm. The optical properties and thermal stability are also characterized. Based on the experimental results, it is deduced that the structure of as-prepared material carbon nitride has polyether structure.

scholarly journals BIORREMEDIATION OF EMERGING POLLUTANTS WITH THE USE OF STRUCTURED MATERIALS

2017 ◽  
Vol 14 (28) ◽  
pp. 87-104
Author(s):  
Mima Sales Loiola ROSA ◽  
Luís Antônio Oliveira NUNES ◽  
Ives Brian Campelo Leite SILVA ◽  
Francisco Cardaso FIGUEIREDO ◽  
José Ribeiro dos SANTOS JUNIOR
Keyword(s):  
Emerging Pollutants ◽  
Energy Dispersive ◽  
Chemical Adsorption ◽  
X Ray Diffraction ◽  
Structured Materials ◽  
X Ray ◽  
Electron Microscopies ◽  
Bioremediation Processes ◽  
Scanning Electron

Human activities in industry, transportation, agriculture and urbanization have been generating the release of emerging pollutants, in other words substances resistant especially in water bodies such as drugs, endocrine disruptors, heavy metals, textile dyes, chloride compounds, nitro phenols and pesticides. For the treatment of systems reached by these emerging pollutants, the bioremediation process has been used worldwide, and consists in using microorganisms that degrade pollutants. This process can be potentiated using structured materials that immobilize the microorganisms by physical or chemical adsorption and transports them to the pollutant. This review highlights the characterization of the structured immobilized or free materials by Scanning Electron Microscopies (SEM) and Transmission (TEM), Energy Dispersive Spectroscopy (EDS), Energy Dispersive X-ray Analysis (EDAX), Fourier transform infrared spectroscopy (FTIR), X-ray Diffraction (XRD) and the influence of the pH on immobilization and bioremediation processes.

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.

Preliminary Preparation and Characterization Studies of Cellulose from Merbau (Intsia bijuga)

2012 ◽  
Vol 620 ◽  
pp. 314-319
Author(s):  
Nur Amira Mamat Razali ◽  
Fauziah Abdul Aziz ◽  
Saadah Abdul Rahman
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Alkaline Treatment ◽  
Raw Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Preliminary Preparation ◽  
Characterization Studies ◽  
Scanning Electron

Hardwood is wood from angiosperm trees. The characteristic of hardwood include flowers, endosperm within seeds and the production of fruits that contain the seeds. This paper aims to discuss the preparation and characterization of cellulose obtained from hardwood. The hardwood Merbau (Intsia bijuga) was chosen as raw material in this study. Alkaline treatment and delignification methods were used for the preparation of cellulose. Acid hydrolysis was employed to produce cellulose nanocrystal (CNC). The treated and untreated samples were characterized using x-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). The final product, from both trated and untreated samples were then compared.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

Characterization of hydrofluoric acid treated Y–Ba–Cu–O oxides

1989 ◽  
Vol 4 (6) ◽  
pp. 1320-1325 ◽  
Author(s):  
Q. X. Jia ◽  
W. A. Anderson
Keyword(s):  
Hydrofluoric Acid ◽  
Electron Spectroscopy ◽  
Auger Electron ◽  
Surface Passivation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Zero Resistance ◽  
Reaction With Water ◽  
Scanning Electron

Effects of hydrofluoric acid (HF) treatment on the properties of Y–Ba–Cu–O oxides were investigated. No obvious etching of bulk Y–Ba–Cu–O and no degradation of zero resistance temperature were observed even though the oxides were placed into 49% HF solution for up to 20 h. Surface passivation of Y–Ba–Cu–O due to HF immersion was verified by subsequent immersion of Y–Ba–Cu–O in water. A thin layer of amorphous fluoride formed on the surface of the Y–Ba–Cu–O during HF treatment, which limited further reaction between Y–Ba–Cu–O and HF, and later reaction with water. Thin film Y–Ba–Cu–O was passivated by HF vapors and showed no degradation in Tc-zero after 30 min immersion in water. The properties of the surface layer of Y–Ba–Cu–O oxide after HF treatment are reported from Auger electron spectroscopy, x-ray diffraction, and scanning electron microscopy studies.

Isolation and characterization of lignocellulosic fiber from jute bast by the organic solvent degumming system: an alkali-free method

2021 ◽  
pp. 004051752110154
Author(s):  
Zhihui Qin ◽  
Shuyuan Zhao ◽  
Liu Liu ◽  
Zhaohe Shi ◽  
Longdi Cheng ◽  
...  
Keyword(s):  
National Standards ◽  
X Ray Diffraction ◽  
High Concentration ◽  
X Ray ◽  
Lignocellulosic Fibers ◽  
Lignocellulosic Fiber ◽  
Isolation And Characterization ◽  
Alkali Consumption ◽  
Scanning Electron

Degumming is the dominant method for insolating lignocellulosic fibers in textile applications. Traditional alkaline degumming (TAL), as a common method, requires a high-concentration alkali and has been a severe challenge to the environment. In the research reported here, the possibility of innovative jute degumming by organic solvents 1-2 propylene glycol and a combination of additive green oxygen (GO-OS) was studied. The results revealed that fibers could be extracted by this system (under condition of 0.9% GO-OS, 180°C, 120 min), and obtained fibers with higher breaking tenacity (7.1 cN/dtex), yield (65.7%), breaking elongation (2.87%) and residual gum (11.7%), which all meet the requirement of the relevant Chinese Textile National Standards. Notably, the required reaction time (120 min) of the GO-OS system was 180 min shorter than that of the TAL method. Furthermore, the modifications introduced by the degumming effect on physicochemical aspects were characterized and confirmed by Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray diffraction. This study provides a promising degumming method for separating jute lignocellulose without acid and alkali consumption.

Characterization of a coating for radioprotection, by X-ray diffraction, scanning electron microscopy, and dispersive energy spectroscopy

2022 ◽  
Vol 321 ◽  
pp. 126326
Author(s):  
Gladis Aparecida Galindo Reisemberger de Souza ◽  
Ramón Sigifredo Cortés Paredes ◽  
Frieda Saicla Barros ◽  
Gustavo Bavaresco Sucharski ◽  
Sebastião Ribeiro Junior ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

scholarly journals Investigations of M3Al8O15:Eu3+,Dy3+ (M = Ba, Ca, Mg) phosphors

2016 ◽  
Vol 34 (2) ◽  
pp. 412-417
Author(s):  
Esra Öztürk
Keyword(s):  
Electron Microscopy ◽  
Solid State Reaction Method ◽  
Morphological Characterization ◽  
X Ray Diffraction ◽  
Reaction Method ◽  
X Ray ◽  
Three Samples ◽  
Scanning Electron ◽  
The Eu

AbstractIn this work, aluminate type phosphorescence materials were synthesized via the solid state reaction method and the photoluminescence (PL) properties, including excitation and emission bands, were investigated considering the effect of trace amounts of activator (Eu3+) and co-activator (Dy3+). The estimated thermal behavior of the samples at certain temperatures (> 1000 °C) during heat treatment was characterized by differential thermal analysis (DTA) and thermogravimetry (TG). The possible phase formation was characterized by X-ray diffraction (XRD). The morphological characterization of the samples was performed by scanning electron microscopy (SEM). The PL analysis of three samples showed maximum emission bands at around 610 nm, and additionally near 589 nm, 648 nm and 695 nm. The bands were attributed to typical transitions of the Eu3+ ions.

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