scholarly journals Synthesis and Characterization of New Ferrite-Lignin Hybrids

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2495
Author(s):  
Iuliana Spiridon ◽  
Ioan-Andrei Dascalu ◽  
Adina Coroaba ◽  
Irina Apostol ◽  
Mircea Nicolae Palamaru ◽  
...  

The paper presents the synthesis and characterization of new cobalt ferrite-lignin hybrids. The hybrids were obtained through the combustion of cobalt nitrate and ferric nitrate, two kinds of lignin being used as combustion agents. The temperatures of calcination were 500 °C and 900 °C, respectively. The hybrids were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), and X-ray photoelectron spectroscopy (XPS). The magnetic properties were also assessed by vibrating sample magnetometer system (VSM). This facile synthesis method made it possible to obtain cobalt ferrite-lignin hybrids with a spinel structure. Their particle sizes and crystallite sizes have increased with an increment in the calcination temperature. A different occupancy of cations at octahedral and tetrahedral sites also occurred upon the increase in temperature. The hybrids comprising organic lignin presented the best magnetic properties.

2020 ◽  
Vol 43 (1) ◽  
pp. 26-42 ◽  
Author(s):  
Zahra Hajian Karahroudi ◽  
Kambiz Hedayati ◽  
Mojtaba Goodarzi

AbstractThis study presents a preparation of SrFe12O19– SrTiO3 nanocomposite synthesis via the green auto-combustion method. At first, SrFe12O19 nanoparticles were synthesized as a core and then, SrTiO3 nanoparticles were prepared as a shell for it to manufacture SrFe12O19–SrTiO3 nanocomposite. A novel sol-gel auto-combustion green synthesis method has been used with lemon juice as a capping agent. The prepared SrFe12O19–SrTiO3 nanocomposites were characterized by using several techniques to characterize their structural, morphological and magnetic properties. The crystal structures of the nanocomposite were investigated via X-ray diffraction (XRD). The morphology of SrFe12O19– SrTiO3 nanocomposite was studied by using a scanning electron microscope (SEM). The elemental composition of the materials was analyzed by an energy-dispersive X-ray (EDX). Magnetic properties and hysteresis loop of nanopowder were characterized via vibrating sample magnetometer (VSM) in the room temperature. Fourier transform infrared spectroscopy (FTIR) spectra of the samples showed the molecular bands of nanoparticles. Also, the photocatalytic behavior of nanocomposites has been checked by the degradation of azo dyes under irradiation of ultraviolet light.


2000 ◽  
Vol 15 (10) ◽  
pp. 2076-2079
Author(s):  
Chika Nozaki ◽  
Takashi Yamada ◽  
Kenji Tabata ◽  
Eiji Suzuki

Synthesis of a rutile-type lead-substituted tin oxide with (110) face was investigated. The characterization was performed by x-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, infrared spectroscopy, x-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area measurements. The homogeneous rutile-type lead-substituted tin oxide was obtained until 4.1 mol% of tin was substituted with lead. The surface of obtained oxide had a homogeneously lead-substituted (110) face.


2002 ◽  
Vol 718 ◽  
Author(s):  
Job Rijssenbeek ◽  
Sylvie Malo ◽  
Takashi Saito ◽  
Vincent Caignaert ◽  
Masaki Azuma ◽  
...  

AbstractPerovskite-like mixed metal ruthenates are of interest owing to their varied electronic and magnetic properties, which are heavily dependent on the ordering of the transition metals. We report the synthesis and structural characterization of the first 1:2 ordered perovskite ruthenate, Sr3CaRu2O9. The structure was determined from a combination of powder X-ray, electron and neutron diffraction data and is characterized by a 1:2 ordering of Ca2+ and Ru5+ over the sixcoordinate B-sites of the perovskite lattice. Sr3CaRu2O9 is the first example of this structure-type to include a majority metal with d electrons (Ru(V), d3). The relationship of this material to the K2NiF4-type Sr1.5Ca0.5RuO4 (i.e., Sr3CaRu2O8) highlights the dramatic effects of the ruthenium valence on the resultant structure. Remarkably, these two structures can be quantitatively interconverted by the appropriate choice of reaction temperature and atmosphere.


2013 ◽  
Vol 203-204 ◽  
pp. 81-85 ◽  
Author(s):  
Małgorzata Zienkiewicz-Strzałka ◽  
Marek Rotko ◽  
Stanislaw Pikus

This paper reports, for the first time, synthesis and characterization of new bifunctional materials containing platinum and silver ions deposited on mesoporous ordered silica SBA-15. Both types of ions were incorporated on silica surface during adsorption from water solutions containing various amounts of dissolved tetraamineplatinum(II) dichloride and diamminesilver(I) hydroxide or tetraamineplatinum(II) dichloride and diamminesilver(I) chloride complexes. The silanol groups on silica surface play important role in adsorption mechanism and one of the most commonly used technique for their characterization is photoacoustic spectroscopy. This technique provides clear evidence of successfully incorporation two types of precious metal ions (Pt and Ag) on SBA-15 surface. The decomposition process of absorbed complexes was investigated according to high temperature in helium. The products of decomposition were analyzed by mass spectrometer. Obtained results show that decomposition temperature of platinum and silver complexes are quite vary. Similarly mechanisms of decomposition of ligands from silver and platinum complexes are also different. Moreover, the structural and chemical properties of Pt,Ag-SBA-15 samples were characterized by X-ray diffraction (XRD), nitrogen adsorption-desorption, transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS).


Crystals ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 466
Author(s):  
Loisangela Álvarez ◽  
Blanca Rojas de Gascue ◽  
Rolando J. Tremont ◽  
Edgar Márquez ◽  
Euclides J. Velazco

A new compound, Bi2O2CO3:Al, was synthesized by the coprecipitation method. The characterization was done by X-ray diffraction (XRD), Fourier transformed infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), electronic scanning microscopy (SEM), and energy dispersive X-ray spectroscopy (EDX). The characterization methods allowed to identify the Bi2O2CO3:Al compound, such as the Al-doped Bi2O2CO3 by XRD, the anionic part (CO32−) by FTIR, and the presence of aluminum in the compound by XPS and EDX. It was confirmed to have a nanostructure like a nanosheet and a microstructure that resembles a type sponge by SEM.


e-Polymers ◽  
2017 ◽  
Vol 17 (1) ◽  
pp. 65-70 ◽  
Author(s):  
Chunhua Luo ◽  
Meijuan Qian ◽  
Qiujing Dong

AbstractThermosensitive PNIPAM-coated Au nanoparticles (AuNPs@P(NIPAM-co-MADMAC)) were synthesized by the radical “grafting through” copolymerization of 4-methacryloyloxy-4′-dimethylaminochalcone (MADMAC), MAEL-capped AuNPs and N-isopropylacrylamide (NIPAM) using azobisisobutyronitrile (AIBN) as the initiator. AuNPs@P(NIPAM-co-MADMAC) were characterized by transmission electron microscopy (TEM), ultraviolet-visible (UV-Vis) spectroscopy, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), 1H nuclear magnetic resonance (NMR), and Fourier transform infrared (FTIR) spectroscopy. AuNPs@P(NIPAM-co-MADMAC) exhibited thermo-sensitivity from poly(NIPAM-co-MADMAC) chains and sensitive fluorescence from the MADMAC group. AuNPs@P(NIPAM-co-MADMAC) showed weak fluorescence after the temperature increased from 25°C to 45°C, or after β-cyclodextrin (β-CD) was added. Furthermore, it exhibited strong fluorescence when the solvent was changed to ethanol or chloroform.


2019 ◽  
Vol 966 ◽  
pp. 237-242
Author(s):  
Fahmi Astuti ◽  
Mizuki Miyajima ◽  
Takahito Fukuda ◽  
Masashi Kodani ◽  
Takehito Nakano ◽  
...  

Polycrystalline rubidium superoxide (RbO2) has been synthesized by using solution method followed by the reaction process under the cooling condition of-40 °C. X-ray Powder Diffraction (XRD) spectra showed that RbO2 was successfully synthesized by this method. The magnetic susceptibility and pulsed muon spin relaxation (μSR) measurements were carried out in order to study the magnetic properties of RbO2.


2005 ◽  
Vol 494 ◽  
pp. 537-542 ◽  
Author(s):  
M. Radić ◽  
N. Ignjatović ◽  
Zoran Nedić ◽  
M. Mitrić ◽  
Dejan Miličević ◽  
...  

In this paper we report the results on synthesis of a composite biomaterial based on biphasic calcium phosphate (BCP) and poly-(DL-lactide-co-glycolide) (DLPLG). Besides, we have investigated the influence of new synthesis method on the structure and characteristics of the composite. The synthesis of biphasic calcium phosphate from Ca(NO3)2 x 4H2O and (NH4)3 PO4 in alkali environment was performed by means of precipitation technique. Composite material BCP/DLPLG was first prepared from commercial granules using chemical methods. Powdered polymer DLPLG was then homogenized at appropriate ratio with addition of biphasic calcium phosphate into the suspension. All samples were characterized by DSC, IR, X-Ray and SEM techniques.


1999 ◽  
Vol 14 (3) ◽  
pp. 1137-1141 ◽  
Author(s):  
Jie Yu ◽  
E. G. Wang ◽  
Guichang Xu

B–C–N compounds were prepared on molybdenum by means of bias-assisted hot filament chemical vapor deposition (HFCVD). Effect of the substrate temperature (Ts) on the growth of B–C–N films has been investigated systematically by x-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) based on the detailed analysis and calculation of the XPS. The substrate temperature plays a key role in the formation of the bonding states, the composition, and the surface morphology. Boron carbonitride is the main phase at all depositing temperatures, and the obtained compounds are as follows: B0.83C0.17 + B0.39C0.35N0.26 at 873 K, B0.30C0.34N0.36 at 973 K, B0.64C0.36 + B0.51C0.23N0.26 at 1073 K, B0.51C0.31N0.18 at 1173 K, and B0.37C0.54N0.09 at 1273 K.


2021 ◽  
Vol 1195 (1) ◽  
pp. 012047
Author(s):  
L D Anbealagan ◽  
T L Chew ◽  
Y F Yeong ◽  
Z A Jawad ◽  
C D Ho

Abstract Over the years, functionalization of zeolite is gaining popularity among researchers to further modify the properties of the zeolite for wide applications. The procedure of functionalization is crucial to ensure that the framework and structure of the zeolite would not be destroyed by the functionalization process. In this work, zeolite AlPO-18 was synthesized via hydrothermal synthesis method and functionalized by (3-Aminopropyl) triethoxysilane (APTES). The effect of the APTES functionalization on zeolite AlPO-18 was investigated in this work. Both unfunctionalized and silane-functionalized zeolite AlPO-18 were characterized using Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and Thermogravimetric analysis (TGA) for their properties. The morphology and the composition of the elements present in zeolite AlPO-18 and zeolite NH2-AlPO-18 were examined using Field Emission Scanning Electron Microscopy (FESEM) and Energy-Dispersive spectroscopy (EDX) respectively. The XRD pattern of NH2-AlPO-18 was similar to that of zeolite AlPO-18, however, the intensity of the peaks was lower compared to zeolite AlPO-18. Based on the FTIR spectra, the presence of N-H stretching and bending vibration band of aminosilane were observed in the NH2-AlPO-18 sample. According to FESEM images, the morphology of NH2-AlPO-18 was comparable to that of zeolite AlPO-18 even after functionalization, proving that functionalization of aminosilane on zeolite does not affect on the zeolite structure. Besides that, EDX proves the presence of 3.02 % of element N in the NH2-AlPO-18 sample which is absent in the zeolite AlPO-18 sample. All of the characterizations evinced the presence of aminosilane, APTES in the NH2-AlPO-18 sample.


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