Synthesis of (2D) MNPs nanosheets of nickel ferrite using a low-cost co-precipitation process

2018 ◽  
Vol 232-235 ◽  
pp. 48-54 ◽  
Author(s):  
N. Hosni ◽  
K. Zehani ◽  
R. Pires Brazuna ◽  
J. Moscovici ◽  
L. Bessais ◽  
...  
2018 ◽  
Vol 34 (5) ◽  
pp. 2577-2582
Author(s):  
Mohamed H. H. Mahmoud ◽  
Mahmoud M. Hessien

Nanomagnetic ferrite materials are of great technological importance in several industries due to their high performance, ease of preparation and low cost. The ferrite properties are based on composition, structure and methods of preparation. Nickel ferrite, NiFe2O4, was prepared by the simple microwave assisted-hydrothermal method. Nickel chloride and ferric chloride solutions (stoichiometric ratio of 1: 2 respectively) were mixed, the pH was raised to 10.5 and the mixture was heated at 180 °C in a closed Teflon vessel using a microwave oven at different periods of time (2 - 24 h). The formed powders were examined by XRD, TEM, and VSM. The intensity of nickel-ferrite in the XRD patterns increased with time owing to increase in crystallinity of the formed phase. The TEM images showed that, the size was in the range of 20-40 nm and contents of fine particles noticeably decreased with increasing reaction time to 4-6 hrs and contents of more regular cubic particles are formed. The NiFe2O4 magnetization was continuesly increased with raising the heating time from 2h (9 emu/g) to 24 h (43 emu/g) which may be due to the high purity and crystallinity of the formed NiFe2O4. The results showed that the properties of the formed ferrite can be tailored by controlling the heating time. Microwave assisted co-precipitation followed by hydrothermal digestion resulted in a substance of good homogeneity and crystallinity at a short time.


2013 ◽  
Vol 13 (4) ◽  
pp. 1109-1115
Author(s):  
Duc Canh Nguyen ◽  
Hyun Ju Park ◽  
Seok Dockko ◽  
Moo Young Han

Arsenic pollution has become a dominant environmental concern in recent years. Various techniques for arsenic removal from water have been developed. However, these techniques efficiently remove arsenic from drinking water but require toxic and expensive chemicals and generate a large amount of exhaust sludge, which is not always regenerable. In this study a novel Fe-Mn-Si oxide material was prepared from environmentally friendly and low-cost materials through a co-precipitation process. Batch adsorption experiments were conducted to study adsorption kinetics, adsorption capacity and the effect of temperature and pH on the adsorption of arsenic on Fe-Mn-Si oxide. The maximum adsorption capacity was found to be 9.62, 10.18, and 10.50 mg/g at 25, 35, and 45 °C, respectively. The results compare favorably with those obtained using other adsorbents. The used Fe-Mn-Si oxide could be regenerated using a NaOH solution; 73.4% of the adsorbed arsenic was desorbed by 0.2 N NaOH. Results from this study demonstrate the potential usability of Fe-Mn-Si oxide as a good arsenic-selective adsorbent.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Robert Christie

Abstract This paper presents an overview of the general chemical principles underlying the structures, synthesis and technical performance of azo pigments, the dominant chemical class of industrial organic pigments in the yellow, orange, and red shade areas, both numerically and in terms of tonnage manufactured. A description of the most significant historical features in this group of pigments is provided, starting from the discovery of the chemistry on which azo colorants are based by Griess in the mid-nineteenth century, through the commercial introduction of the most important classical azo pigments in the early twentieth century, including products known as the Hansa Yellows, β-naphthol reds, including metal salt pigments, and the diarylide yellows and oranges, to the development in the 1950s and 1960s of two classes of azo pigments that exhibit high performance, disazo condensation pigments and benzimidazolone-based azo pigments. A feature that complicates the description of the chemical structures of azo pigments is that they exist in the solid state as the ketohydrazone rather than the hydroxyazo form, in which they have been traditionally been illustrated. Numerous structural studies conducted over the years on an extensive range of azo pigments have demonstrated this feature. In this text, they are referred to throughout as azo (hydrazone) pigments. Since a common synthetic procedure is used in the manufacture of virtually all azo (hydrazone) pigments, this is discussed in some detail, including practical aspects. The procedure brings together two organic components as the fundamental starting materials, a diazo component and a coupling component. An important reason for the dominance of azo (hydrazone) pigments is that they are highly cost-effective. The syntheses generally involve low cost, commodity organic starting materials and are carried out in water as the reaction solvent, which offers obvious economic and environmental advantages. The versatility of the approach means that an immense number of products may be prepared, so that they have been adapted structurally to meet the requirements of many applications. On an industrial scale, the processes are straightforward, making use of simple, multi-purpose chemical plant. Azo pigments may be produced in virtually quantitative yields and the processes are carried out at or below ambient temperatures, thus presenting low energy requirements. Finally, provided that careful control of the reaction conditions is maintained, azo pigments may be prepared directly by an aqueous precipitation process that can optimise physical form, with control of particle size distribution, crystalline structure, and surface character. The applications of azo pigments are outlined, with more detail reserved for subsequent papers on individual products.


2011 ◽  
Author(s):  
Darminto ◽  
Machida N. Cholishoh ◽  
Feby A. Perdana ◽  
Malik A. Baqiya ◽  
Mashuri ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1617
Author(s):  
Silviu-Adrian Predoi ◽  
Carmen Steluta Ciobanu ◽  
Mikael Motelica-Heino ◽  
Mariana Carmen Chifiriuc ◽  
Monica Luminita Badea ◽  
...  

In the present study, a new low-cost bioceramic nanocomposite based on porous hydroxyapatite (HAp) and cetyl trimethyl ammonium bromide (CTAB) as surfactant was successfully obtained by a simple chemical co-precipitation. The composition and structure of the HAp-CTAB were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscope (SEM) equipped with an energy dispersive X-ray (EDX) spectrometer, and N2 adsorption/desorption analysis. The capacity of HAp-CTAB nanocomposites to remove the lead ions from aqueous solutions was studied by adsorption batch experiments and proved by Langmuir and Freundlich models. The Pb2+ removal efficiency of HAp-CTAB biocomposite was also confirmed by non-destructive ultrasound studies. The cytotoxicity assays showed that the HAp-CTAB nanocomposites did not induce any significant morphological changes of HeLa cells after 24 h of incubation or other toxic effects. Taken together, our results suggests that the obtained porous HAp-CTAB powder could be used for the decontamination of water polluted with heavy metals, such as Pb2+.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Dian Gong ◽  
Gaofeng Zeng

AbstractTransition metal oxides are the potential catalysts to replace noble-metal based catalyst for the catalytic combustion of methane due to the tolerable reactivity and low cost. However, these catalysts are challenged by the low temperature reactivity. Herein, the surface defective Co3O4 nanoplates are realized through a facile co-precipitation and thermal reduction method with the association of GO. The resultant catalysts (CoGO50) demonstrate a superior low-temperature reactivity for the methane oxidation to CO2 and H2O in comparison with the common Co3O4 catalyst. The reliable stability of CoGO50 catalyst was proved by 80 h testing with intermittent feeding of water vapor. The experimental analysis demonstrates that the presence of a small amount of GO significantly affects the catalysts in surface valence state, active oxygen species and surface oxygen vacancies through reacting with the cobalt oxide as a reductant. Moreover, GO plays as 2D confine template to form smaller and thinner nanoplates. This work provides a facile method to control the surface properties of catalyst not only for Co3O4 based catalysts but also for wider solid catalysts.


2009 ◽  
Vol 79-82 ◽  
pp. 505-508
Author(s):  
Li Li ◽  
H. Zhao ◽  
Wei Wang ◽  
F.F. Nie

The magnetic Fe3O4 nanoparticles had been synthesized by co-precipitation process and surface treatment by silane coupling agent (KH570). The magnetic Fe3O4/PMMA nanocomposite films were prepared by blend method, and the chemical structure, mechanical properties, surface morphology and the biocompatibility of the nanocomposite films were studied in this work. The magnetic Fe3O4 nanoparticles were well dispersed in the Fe3O4/PMMA nanocomposite films. The strength of the nanocomposite films, as well as the strain, decreased first and then increased with the increasing of the nanoparticles. The hemolytic ratio indicated that the nanocomposite films had a better blood compatibility.


RSC Advances ◽  
2016 ◽  
Vol 6 (54) ◽  
pp. 49228-49235 ◽  
Author(s):  
Chengwei Gao ◽  
Baojun Li ◽  
Ning Chen ◽  
Jie Ding ◽  
Qiang Cai ◽  
...  

Fe3O4/HNT@rGO composite (FHGC) was fabricated via a facile co-precipitation process, followed by heat treatment. For RhB and As5+removal, the high performance and easy separation of FHGC highlight its potential application in water treatment.


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