Effect of mechanical alloying on the synthesis of Fe-TiC nanocomposite

2017 ◽  
Vol 24 (5) ◽  
pp. 739-745 ◽  
Author(s):  
Ali Reza Jam ◽  
Mansour Razavi ◽  
Leila Nikzad
Keyword(s):  
Mechanical Alloying ◽  
Crystallite Size ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Sem Images ◽  
The Mean ◽  
Xrd Patterns ◽  
Tic Particulates ◽  
Mean Strain ◽  
Microstructural Studies

AbstractTiC particulates-reinforced Fe-based nanocomposites were fabricated using ferrotitanium and carbon black powders by mechanical alloying (MA). The raw materials were milled in a planetary ball mill and sampled in different times. The phase type, crystallite size, and mean strain of milled samples were estimated by X-ray diffraction (XRD) instrument. The scanning electron microscopy (SEM) images of milled powders showed that titanium carbide was synthesized gradually after 90 min of milling and its formation was completed after 5 h and the crystallite size of the produced carbide was in nanometer scale. Increasing milling times gave rise to the reduction of crystallite size as well as the augmentation of the mean strain. Microstructural studies confirmed the accuracy of crystallite size calculations by XRD patterns.

scholarly journals Investigation of Ferrimagnetic Sr-hexaferrite Nanocrystals for Clinical Hyperthermia

2021 ◽  
pp. X
Author(s):  
Burcu ERTUĞ
Keyword(s):  
Crystallite Size ◽  
Room Temperature ◽  
Vibrating Sample Magnetometry ◽  
Sem Images ◽  
Ceramic Method ◽  
X Ray ◽  
The Mean ◽  
Xrd Patterns ◽  
Potential Use ◽  
Scanning Electron

Sr-hexaferrite samples were produced via the conventional ceramic method. X-ray diffractometry (XRD) patterns confirmed the single nanocrystal phase as Sr-hexaferrite where any pattern peaks of unreacted Fe2O3 phase were  not detected. The mean crystallite size values were determined to be 44.12±3.4nm and 41.2±3.2nm for SHF-O1 and SHF-O2, respectively. The chemical bonding peaks of our sample indicated that the structure of Sr-hexaferrite formation was confirmed by FTIR spectra result. Scanning electron microscopy (SEM) images indicated clearly observed porosity regions with relative densities as high as 94% and 87% for SHF-O1 and SHF-O2 samples.The vibrating sample magnetometry (VSM) of each sample at 2K and under a magnetic field of 10 kOe yielded saturation magnetizations, Ms of 93.5 and 94.1 emu/g; remanence values, Mr of 76.4 and  67.8 emu/g for SHF-O1 and SHF-O2, respectively. The magnetization loops of both samples indicated a soft ferrimagnetic behaviour in which the saturation magnetizations were higher than those measured  at room temperature in the previous studies. The coercivities, Hc were measured to be 150Oe for both samples. The squareness values, SQR (Mr/Ms) were measured to be high, approximately 0.82 and 0.72 for SHF-O1 and SHF-O2, respectively. Depending on the adequate values of magnetization and coercivity along with small mean crystallite size and low porosity values of the obtained Sr-hexaferrite samples, we estimate that these samples are likely to be evaluated further for the potential use as thermoseeds in the field of clinical hyperthermia.

Effect of Polyvinyl Pyrrolidone Dosage on Barium Ferrite Fibers via Electrospinning

2016 ◽  
Vol 848 ◽  
pp. 333-338
Author(s):  
Yue Guang Chen ◽  
Gui Fang Liu ◽  
Shi Jiao Wang
Keyword(s):  
Barium Ferrite ◽  
Raw Materials ◽  
Precursor Solution ◽  
Vinyl Pyrrolidone ◽  
Dimethyl Formamide ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Vibration Sample Magnetometer ◽  
Poly Vinyl Pyrrolidone ◽  
Xrd Patterns

Barium ferrite micro/nanofibers were successfully prepared via the electrospinning by using dimethyl formamide (DMF) as the solvent, poly vinyl pyrrolidone (PVP) as the spinning auxiliaries and iron nitrate and barium nitrate as raw materials. The effect of poly vinyl pyrrolidone on the structure, morphology, magnetic and microwave absorbing properties were investigated by scanning electron microscope (SEM), X-ray diffraction analysis (XRD), vibration sample magnetometer (VSM) and vector network analyzer (VNA). XRD patterns of the samples confirmed that when the additive content of PVP was up to 10%, (wt%) pure barium ferrite fibers formed under the condition of the same heat treatment. Also, the FE-SEM images showed that the morphology of the fibers improved with the increase of PVP content. Moreover, the VSM results demonstrated that the saturation magnetization can reach 54.7 emu/g when the PVP dosage is 14% (wt%) in the precursor solution.

Investigation of Microstructure and Property of Fe3Al/Al2O3 Composites

2010 ◽  
Vol 150-151 ◽  
pp. 1409-1412 ◽  
Author(s):  
Tao Jiang
Keyword(s):  
Heat Treatment ◽  
Phase Composition ◽  
Mechanical Alloying ◽  
Sintering Process ◽  
Composite Powders ◽  
Al2o3 Composite ◽  
Al2o3 Phase ◽  
The Mean ◽  
Xrd Patterns ◽  
Al2o3 Matrix

The Fe3Al/Al2O3 composites were fabricated by pressureless sintering process. The Fe3Al intermetallics compounds powders were fabricated by mechanical alloying and heat treatment, then the Fe3Al powders and Al2O3 powders were mixed and the Fe3Al/Al2O3 composite powders were prepared, so the Fe3Al/Al2O3 composites were fabricated by sintering process at 1700oC for 2h. The phase composition and microstructure of Fe3Al intermetallics compounds powders produced by mechanical alloying and heat treatment were investigated. The phase composition, microstructure and mechanical properties of the Fe3Al/Al2O3 composites sintered bulks were investigated. The XRD patterns results showed that there existed Fe3Al phase and Al2O3 phase in the sintered composites. The Fe3Al/Al2O3 composites sintered bulks exhibited the homogenous and compact microstructure, the Fe3Al particles were homogenously distributed in the Al2O3 matrix, the mean particles size of Fe3Al intermetallics was about 3-5μm. The Fe3Al/Al2O3 composites exhibited more homogenous and compact microstructure with the increase of Fe3Al content in the Al2O3 matrix. The density and relative density of the Fe3Al/Al2O3 composites increased gradually with the increase of Fe3Al content. The fracture strength and fracture toughness of the Fe3Al/Al2O3 composites increased gradually with the increase of Fe3Al content. The elastic modulus and hardness (HRA) of the Fe3Al/Al2O3 composites decreased gradually with the increase of Fe3Al content.

The Use of the Pseudo-Voigt Function in the Variance Method of X-ray Line-Broadening Analysis

1997 ◽  
Vol 30 (4) ◽  
pp. 427-430 ◽  
Author(s):  
F. Sánchez-Bajo ◽  
F. L. Cumbrera
Keyword(s):  
Crystallite Size ◽  
Original Form ◽  
Line Broadening ◽  
X Ray Diffraction ◽  
Stabilized Zirconia ◽  
X Ray ◽  
Variance Method ◽  
The Mean ◽  
Voigt Function

A modified application of the variance method, using the pseudo-Voigt function as a good approximation to the X-ray diffraction profiles, is proposed in order to obtain microstructural quantities such as the mean crystallite size and root-mean-square (r.m.s.) strain. Whereas the variance method in its original form is applicable only to well separated reflections, this technique can be employed in the cases where there is line-profile overlap. Determination of the mean crystallite size and r.m.s. strain for several crystallographic directions in a nanocrystalline cubic sample of 9-YSZ (yttria-stabilized zirconia) has been performed by means of this procedure.

Synthesis, Characterization and Properties of PANI/(La-Nd Doped BaFe12O19) Composites

2017 ◽  
Vol 727 ◽  
pp. 327-334
Author(s):  
Yan Wang ◽  
Jun Wang ◽  
Xiao Fei Zhang ◽  
Ya Qing Liu
Keyword(s):  
Sol Gel ◽  
Network Analyzer ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Structure Morphology ◽  
Xrd Patterns ◽  
Hexagonal Platelet ◽  
Peak Value ◽  
Properties Of Composites

La-Nd co-doped barium hexaferrites, Ba0.7(LamNdn)0.3Fe12O19 (D-BaM), were successfully prepared by sol-gel method. PANI / D-BaM composites were synthesized by in-situ polymerization in solution. The structure, morphology and properties of samples have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), four-probe conductivity tester and vector network analyzer. The XRD patterns showed that the crystal structure of all the samples exist as M-type phases. The SEM images revealed that the particles presented a hexagonal platelet-like morphology. The magnetic properties could be improved by substitutions of La and Nd ions. The saturation magnetization (Ms) and coercive force (Hc) increased with the change of La / Nd ratio to the maximum at La / Nd = 3:1. The doped particles have also been embedded in conductive PANI to prepare electromagnetic materials, and the conductivity kept on the order of 10-2. The microwave absorbing properties of composites at 30 MHz-6 GHz improved obviously, the peak value of reflection loss could reach-7.5 dB.

Elaboration, Structure and Mössbauer Spectroscopy of Nanostructured Fe100−xSix Powders Elaborated by Mechanical Alloying

SPIN ◽  
2017 ◽  
Vol 07 (02) ◽  
pp. 1750002 ◽  
Author(s):  
M. Hemmous ◽  
A. Guittoum
Keyword(s):  
Magnetic Field ◽  
Solid Solution ◽  
Mechanical Alloying ◽  
Hyperfine Magnetic Field ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
The Mean ◽  
Xrd Studies

We have studied the effect of the silicon concentration on the structural and hyperfine properties of nanostructured Fe[Formula: see text]Six powders ([Formula: see text], 20, 25 and 30[Formula: see text]at.%) prepared by mechanical alloying. The X-ray diffraction (XRD) studies indicated that after 72[Formula: see text]h of milling, the solid solution bcc-[Formula: see text]-Fe(Si) is formed. The grain sizes, [Formula: see text]D[Formula: see text] (nm), decreases with increasing Si concentration and reaches a minimum value of 11[Formula: see text]nm. We have found that the lattice parameter decreases with increasing Si concentration. The changes in values are attributed to the substitutional dissolution of Si in Fe matrix. From the adjustment of Mössbauer spectra, we have shown that the mean hyperfine magnetic field, [Formula: see text]H[Formula: see text] (T), decreases with increasing Si concentration. The substitutional dependence of [Formula: see text]H[Formula: see text] (T) can be attributed to the effect of p electrons Si influencing electrons d of Fe.

scholarly journals Influence of B2O3 doping on synthesis of MgTiO3 ceramics from recycled magnesia-hercynite materials

2021 ◽  
Vol 8 (12) ◽  
pp. 125901
Author(s):  
Xiaodong Jia ◽  
Shuo Mao ◽  
Lin Tian ◽  
Shujiang Chen ◽  
Guohua Li ◽  
...  
Keyword(s):  
Dielectric Properties ◽  
Raw Materials ◽  
Microwave Dielectric Properties ◽  
Synthesis Rate ◽  
Cement Kiln ◽  
X Ray Diffraction ◽  
Optimum Amount ◽  
X Ray ◽  
Microwave Dielectric ◽  
Microstructural Studies

Abstract Herein, magnesium metatitanate (MgTiO3) ceramics were synthesised using recycled magnesia-hercynite (MH) bricks as the raw materials to achieve solid waste reusing of cement kiln refractories. The recycled MH materials were mixed with anatase TiO2 to investigate the effect of addition of doped B2O3 during the synthesis of MgTiO3 ceramics at 1400 °C. Phase compositions and microstructural studies were performed using x-ray diffraction (XRD) and scanning electron microscope (SEM), respectively. In addition, energy-dispersive spectroscopy (EDS) was conducted and the dielectric properties of the samples were studied. Results show that the addition of B2O3 can promote sintering, improve shrinkage, promote densification, stabilise MgTiO3 lattice, and inhibit the formation of MgTiO3. In addition, the presence of appropriate amount of B2O3 can accelerate the material diffusion and result in grain growth through the formation of intercrystalline liquid phase. Results also suggest that an increase in dielectric constant results in a decrease in dielectric loss. It was concluded that 2 wt% was the optimum amount of B2O3 required to obtain the most favourable synthesis rate of MgTiO3 (98.2%). The samples exhibited a maximum density of 3.69 g·cm−3 and excellent microwave dielectric properties at ε r = 18.28 and tanδ = 0.086.

Synthesis and Characterization of Cadmium with Titanium Oxide (Cd-TiO2) Nanocomposite: Testing its Antibacterial Effect

2021 ◽  
Vol 12 (4) ◽  
pp. 2523-2529
Author(s):  
Daniel Sam N ◽  
Anish C I ◽  
Sabeena G ◽  
Rajaduraipandian S ◽  
Manobala ◽  
...  
Keyword(s):  
Sol Gel ◽  
Gram Negative Bacteria ◽  
X Ray Diffraction ◽  
Sem Images ◽  
Gram Negative ◽  
X Ray ◽  
Weight Percentage ◽  
Inhibition Concentration ◽  
Xrd Patterns

Sol gel methods were used for the study of the antimicrobial activity of Cd-TiO2 against gram-negative and positive bacteria. These Cd-TiO2 have been characterized by various optical and techniques. They have been exhibited by X-ray diffraction, scanning electron microscopy, ultraviolet spectroscopy, and infrared spectroscopy. The structures of the various XRD patterns indicate that the product has a structure. The particle size of Cd-TiO2 is 35nm. The SEM images confirm the spherical appearance of the sample. The energy X-ray spectra have been confirmed as well and then C, O, Ti, Cd, Pt element are present in Cd-TiO2. The weight percentage of Cadmium is 5.8%, Ti is 51.03%, C is 5.13% and O is 31.75% in Cd-TiO2. BET image shows that the major pore size distribution of Cd-TiO2 is ranged from 2.24 nm. The Cd-TiO2 that the antibacterial activity when tested against the pathogens only gram-negative bacteria such as Pseudomonas. The zone of minimum inhibition concentration was measured in a range of 20mm in 25μl and 30mm in 100μl.

Photocatalytic Comparative Study of TiO2, ZnO, Ag-G-ZnO and Ag-G-TiO2 Nanocomposite Films

2017 ◽  
Vol 751 ◽  
pp. 825-830 ◽  
Author(s):  
Phuri Kalnaowakul ◽  
Tonghathai Phairatana ◽  
Aphichart Rodchanarowan
Keyword(s):  
Colloidal Solution ◽  
Nanocomposite Films ◽  
Blue Dye ◽  
Methylene Blue Dye ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Photocatalytic Activities ◽  
Xrd Patterns

In this study, the photocatalytic properties and morphology of TiO2, ZnO, Ag-graphene-zinc oxide (Ag-G-ZnO) and Ag-graphene-titanium dioxide (Ag-G-TiO2) nanocomposite were compared. The Ag-G-ZnO and Ag-G-TiO2 nanocomposite were successfully prepared by thermal decomposition of colloidal solution. These prepared composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-Vis spectroscopy and photocatalytic activities. The results from XRD patterns show that Ag-G-TiO2 composites and the Ag-G-ZnO nanocomposites were in the form of fcc and hcp crystal structure, respectively. The SEM images show that at calcination of 500 °C for 3 h, the composite thin film of Ag-G-ZnO and Ag-G-TiO2 were homogenous. In the case of the photocatalytic experiments using methylene blue dye (MB) under UV irradiation, the order of the photocatalytic activities from high to low performances are Ag-G-ZnO, Ag-G-TiO2, ZnO and TiO2, respectively.

scholarly journals Effect of Magnesium Borates on the Fire-Retarding Properties of Zinc Borates

2014 ◽  
Vol 2014 ◽  
pp. 1-12 ◽  
Author(s):  
Azmi Seyhun Kipcak ◽  
Nil Baran Acarali ◽  
Emek Moroydor Derun ◽  
Nurcan Tugrul ◽  
Sabriye Piskin
Keyword(s):  
Raw Materials ◽  
High Strength ◽  
High Heat ◽  
Zinc Borate ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Magnesium Borate ◽  
Sem Images ◽  
Ir And Raman Spectroscopies ◽  
Coefficient Of Elasticity

Magnesium borate (MB) is a technical ceramic exhibiting high heat resistance, corrosion resistance, great mechanical strength, great insulation properties, lightweightness, high strength, and a high coefficient of elasticity. Zinc borate (ZB) can be used as a multifunctional synergistic additive in addition to flame retardant additives in polymers. In this study, the raw materials of zinc oxide (ZnO), magnesium oxide (MgO), and boric acid (H3BO3) were used in the mole ratio of 1 : 1 : 9, which was obtained from preexperiments. Using the starting materials, hydrothermal synthesis was applied, and characterisation of the products was performed using X-Ray diffraction (XRD) and Fourier transform infrared (FT-IR) and Raman spectroscopies. The forms of Zn3B6O12·3.5H2O, MgO(B2O3)3·7(H2O), and Mg2(B6O7(OH)6)2·9(H2O) were synthesised successfully. Moreover, the surface morphology was investigated using scanning electron microscopy (SEM), and the B2O3content was determined. In addition, the reaction yields were calculated. The results of the B2O3content analysis were in compliance with the literature values. Examination of the SEM images indicated that the obtained nanoscale minerals had a reaction efficiency ranging between 63–74% for MB and 87–98% for ZB. Finally, the fire-retarding properties of the synthesised pure MBs, pure ZBs, and mixtures of MB and ZB were determined using differential thermal analysis and thermal gravimetry (DTA-TG) and differential scanning calorimetry (DSC).

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