scholarly journals Synthesis, Characterization and Applications of MoO3-Fe3O4 Nanocomposite Material

2019 ◽  
Vol 2 (2) ◽  
Author(s):  
Madhukar Eknath Navgire ◽  
Akash Nagare ◽  
Ganesh Kale ◽  
Sandesh Bhitre

In the present investigation a series of MoO3-Fe3O4 nanocomposite material such as MoO3, Fe3O4, Beta cyclodextrin (b-CD) doped MoO3-Fe3O4 and Graphite doped MoO3-Fe3O4 have been synthesized successfully by co-precipitation method. Synthesized nanomaterials were characterized in detail by XRD, FT-IR, TEM-HRTEM, UV-Vis DRS techniques. The crystalline size was in the range of 10±2 nm. The activity of the prepared material as a heterogeneous catalyst was successfully tested on the organic reaction of synthesis of substituted m-Chloro-Nitrobenzene and it was found to give excellent yield.

2015 ◽  
Vol 645-646 ◽  
pp. 1339-1344 ◽  
Author(s):  
Yan Ting Yin ◽  
Qing Hua Chen ◽  
Ting Ting Yan ◽  
Qing Hua Chen

The objective of this study was to develop a novel silica modified large-sized hydroxyapatite whiskers with improved properties for use in bone repair applications. Large-sized whiskers with a mean length of 250μm were obtained by a hydrothermal co-precipitation method at 150°C, 7.5Mpa in high-pressure reactor. Silica modified hydroxyapatite whiskers were prepared by dissolving TEOS in ethanol solution, then sintering with hydroxyapatite. The compositional and morphological properties of prepared whiskers were studied by means of x-ray diffraction (XRD), Fouier transform infrared (FT-IR), scanning electron microscopy (SEM). The results indicated the evidence of nanosilicon dioxide particles on the surface of HAP whiskers. The size of nanosilicon dioxide particles depends on dropping and stirring rate. Hence, this new type of silica modified large-sized hydroxyapatite whiskers is a valuable candidate for biomedical applications.Key words: hydroxyapatite, hydrothermal co-precipitation, surface modified, whiskers


2013 ◽  
Vol 838-841 ◽  
pp. 2306-2309
Author(s):  
Guang Hua Wang ◽  
Kun Chen ◽  
Wen Bing Li ◽  
Dong Wan ◽  
Qin Hu ◽  
...  

Magnetic modified organobentonite (Fe3O4/CTAB–Bent) was synthesized by chemical co-precipitation method in which CTAB–Bent was firstly achieved via ion–exchange.The composite materials have been characterized by powder X–ray diffraction (XRD), Fourier transform infrared spectroscopy (FT–IR) and Scanning electron microscopy (SEM) . The results revealed that basal spacing of bentonite was increased through organic modification and the Fe3O4 particles synthesized which covering the surfaces of bentonite .Compared with natural bentonite, the adsorption capacity of Fe3O4/CTAB–Bent for Orange II was greatly enhanced and can be easily separated from the reaction medium by an external magnetic field after the treatment.


Catalysts ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 750 ◽  
Author(s):  
Ali M. A. Al-Najar ◽  
Faris A. J. Al-Doghachi ◽  
Ali A. A. Al-Riyahee ◽  
Yun Hin Taufiq-Yap

Pt,Pd,Ni/MgO, Pt,Pd,Ni/Mg0.97La3+0.03O, Pt,Pd,Ni/Mg0.93La3+0.07O, and Pt,Pd,Ni/Mg0.85La3+0.15O (1% of each of the Ni, Pd, and Pt) catalysts were prepared by a surfactant-assisted co-precipitation method. Samples were characterized by the XRD, XPS, XRF, FT-IR, H2-TPR, TEM, the Brunauer–Emmett–Teller (BET) method, and TGA and were tested for the dry reforming of methane (DRM). TEM and thermal gravimetric analysis (TGA) methods were used to analyze the carbon deposition on spent catalysts after 200 h at 900 °C. At a temperature of 900 °C and a 1:1 CH4:CO2 ratio, the tri-metallic Pt,Pd,Ni/Mg0.85La3+0.15O catalyst with a lanthanum promoter showed a higher conversion of CH4 (85.01%) and CO2 (98.97%) compared to the Ni,Pd,Pt/MgO catalysts in the whole temperature range. The selectivity of H2/CO decreased in the following order: Pt,Pd,Ni/Mg0.85La3+0.15O > Pt,Pd,Ni/Mg0.93La3+0.07O > Pt,Pd,Ni/Mg0.97La3+0.03O > Ni,Pd,Pt/MgO. The results indicated that among the catalysts, the Pt,Pd,Ni/Mg0.85La23+0.15O catalyst exhibited the highest activity, making it the most suitable for the dry reforming of methane reaction.


2016 ◽  
Vol 855 ◽  
pp. 47-53
Author(s):  
Ampa Jimtaisong ◽  
Nisakorn Saewan

Inclusion complex of β-cyclodextrin (β-CD) and Plai (Zingiber cassumunar) oil was prepared using a simple co-precipitation method at β-CD to Plai oil in different ratios. The inclusion complexes were characterized using Fourier transform-infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC). The FT-IR absorption bands of inclusion complex at 3600-3200 cm-1 were broader and shifted toward lower frequencies compared with that of pure β-CD (3359 cm-1). DSC of the inclusion complexes showed two endothermic peaks shifted to lower temperatures (90-100°C and 295-300°C) compared to that of β-CD. The different physicochemical characteristic could be an indication of an embedded guest molecule in the β-CD cavities in the inclusion complex preparation.


2015 ◽  
Vol 735 ◽  
pp. 177-181
Author(s):  
Ee Ting Wong ◽  
Pei Cheng Teh ◽  
Kian Hwa Chan ◽  
Ani Idris

The magnetic nanoparticles of manganese-doped magnetite (Mn-Fe2O4) were synthesized by the simple co-precipitation method. The stable Mn2+ and Fe3+ salts in the ratio of 1:2 in aqueous solution, were added into the sodium hydroxide solution to form the Mn-Fe2O4 precipitate at temperature of 95°C. The synthesized nanoparticles were then characterized by Fourier Transform-Infrared Spectroscopy (FT-IR) and X-ray diffraction spectroscopy (XRD). It was then entrapped in the PVA-alginate matrix to form the nanophotoadsorbent in beads form. The synthesized nanoparticles embedded bead was characterized by Scanning Electron Microscopy (SEM). The effects of various parameters, such as contact time, pH, nanoparticles dosage were investigated. The control study was also performed to reveal the performance of photo-adsorbent towards the Cu (II) removal under the light and dark conditions. It was found that the removal efficiency of the Cu (II) achieved 97.07% (1.46ppm) which complied to the WHO drinking water standard of less than 1.5ppm after 180 min treatment.


2020 ◽  
pp. 13-20
Author(s):  
Luma Ahmed ◽  
Eitemad S. Fadhil ◽  
Ayad F. Mohammed

This article describes the synthesis of ZnO nanoparticles (Nps) using the co-precipitation method and then calcinated at 500oC for 2 h. The photo activity of ZnO nanoparticles was examined in photo decolorization of methyl green dye under artificial UV -A light. This prepared photocatalyst (ZnO Np) was modified his surface by 2% Ag doped using the photo deposition method under inert gas for 3h. The characterization of undoped and 2% Ag doped ZnO Nps were estimated by Fourier-transform infrared spectroscopy (FT-IR), X-ray Diffraction (XRD), and Atomic force microscopy (AFM). In FT-IR analysis, the new peaks occurred around 624-778 cm-1 confirmed the Ag really is doped on prepared ZnO Np. Based on data from XRD, the mean crystal size was reduced with doped the 2% Ag. The AFM images for the prepared photocatalysts ensure that the shapes of all samples are semi-spherical with nanometer size. Series of kinetics experiments were performed for the photocatalytic decolourization of methyl green dye using undoped and 2% Ag doped ZnO nanoparticle and found to be pseudo-first-order kinetics.


Author(s):  
Pelin Aktaş

BaTi5O11 has been widely researched due to its unique microwave properties. Conventionally it is challenging to obtain this compound as a single phase. The BaTi5O11 was synthesized via co-precipitation technique using an aqueous solution of titanium(IV)(triethanolaminato) isopropoxide, barium nitrate and ammonia as precursors which are stable in an aqueous media. The phase evolution, purity, and structure were identified by X-ray diffraction (XRD), scanning electron microscope (SEM) and energy dispersive X-ray (EDX) spectroscopy analysis. The desired BaTi5O11 structure was obtained by calcination at 900?C. Furthermore, the structure is characterized by TGA, FT-IR and Raman studies. The study showed that the particles were between 80 and 120 nm in size and the average crystallite size was determined from the Scherrer formula as 68.1 nm at 900?C.


2016 ◽  
Vol 25 (6) ◽  
pp. 096369351602500 ◽  
Author(s):  
Ruimin Fu ◽  
Mingfu Zhu

Nowadays, the hummers method for preparation of graphene oxide (GO) was improved. The grapheme oxide @ Fe3O4 magnetic nanocomposites were synthesized by co-precipitation method. After analysing the morphology and structure of obtained nanocomposites by X-ray diffraction (XRD), transmission electron microscope (TEM) and Fourier transform infrared (FT-IR) spectroscopy, the result was shown as follows. The particle size of Fe3O4 in nanocomposites is 30 nm. Many functional groups are found in grapheme oxide, and such groups could be used to bind with the drug. In the test for magnetic properties, the nanocomposites gathered rapidly in the vicinity of the permanent magnet. The nanocomposites, with high superparamagnetism, can be used in the following applications: drug targeting transports, drug carrier, and diagnosis assistant system.


2020 ◽  
Vol 1159 ◽  
pp. 60-66
Author(s):  
J.R. Sheeba ◽  
Sathasivam Radhika ◽  
C.M. Padma

Pure and copper doped tin oxide nanoparticles were synthesized by co-precipitation method and are characterized by XRD, SEM, EDAX, UV-Visible, photoluminescence, and FT-IR analysis techniques. Tetragonal rutile structure is confirmed from XRD and the crystallite size is found to be between 3.8nm and 4.8nm. The optical band gap is observed from UV-Vis spectrum and is found to be 3.99eV and 3.93eV for tin oxide and copper doped tin oxide respectively. The optical band gap of pure and Copper doped tin oxide were blue shifted due to quantum confinement. Photoluminescence spectrum shows UV, blue and green emission peaks.


2021 ◽  
Vol 10 (3) ◽  
pp. xx-xx
Author(s):  
Thu Le Dieu ◽  
Hoang Tran Vinh

In this study, heavy metal ions or organic in the aqueous solution are removed by adsorbent without filtration or centrifugation as well as incorporate magnetic materials into the adsorbent. A composite film GO/PVA from PVA and self – synthesized GO by co - precipitation method has synthesized successfully. This composite was characterized by XRD, SEM, FT-IR to evaluate the properties of this material. The results showed that there was an interaction between GO and PVA so we have tested the adsorption capacity of this composite with Co(II) ions and the obtained efficiency of this process was 99.5% with the initial concentration of solution is 20 mg.L-1. This film is completely capable of removing heavy metal ions from waste water.


Sign in / Sign up

Export Citation Format

Share Document