scholarly journals Surface Treatment of Industrial-Grade Magnetite Particles for Enhanced Thermal Stability and Mitigating Paint Contaminants

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2299
Author(s):  
Mohua Sinhababu ◽  
Anurag Roy ◽  
Narendra Kumar ◽  
Monojit Dutta ◽  
Senthilarasu Sundaram ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Surface Treatment ◽  
Photoelectron Spectroscopy ◽  
Large Scale ◽  
Low Cost ◽  
High Surface ◽  
Color Difference ◽  
X Ray ◽  
Industrial Grade ◽  
Paint Industry

Pigments can retain their color for many centuries and can withstand the effects of light and weather. The paint industry suffers from issues like aggressive moisture, corrosion, and further environmental contamination of the pigment materials. Low-cost, long-lasting, and large-scale pigments are highly desirable to protect against the challenges of contamination that exist in the paint industry. This exploratory study reinforces the color and thermal stability of industrial-grade (IG) magnetite (Fe3O4). IG Fe3O4 pigments were further considered for surface treatment with sodium hexametaphosphate (SHMP). This metaphosphate hexamer sequestrant provides good dispersion ability and a high surface energy giving thermal and dust protection to the pigment. Various physicochemical characterizations were employed to understand the effectiveness of this treatment across various temperatures (180–300 °C). The X-ray diffraction, Raman, and X-ray photoelectron spectroscopy techniques signify that the SHMP-treated Fe3O4 acquired magnetite phase stability up to 300 °C. In addition, the delta-E color difference method was also adopted to measure the effective pigment properties, where the delta-E value significantly decreased from 8.77 to 0.84 once treated with SHMP at 300 °C. The distinct color retention at 300 °C and the improved dispersion properties of surface-treated Fe3O4 positions this pigment as a robust candidate for high-temperature paint and coating applications. This study further encompasses an effort to design low-cost, large-scale, and thermally stable pigments that can protect against UV-rays, dust, corrosion, and other color contaminants that are endured by building paints.

scholarly journals Role of Ag+ in the Bioleaching of Arsenopyrite by Acidithiobacillus ferrooxidans

Metals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 403
Author(s):  
Yan Zhang ◽  
Qian Li ◽  
Xiaoliang Liu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Acidithiobacillus Ferrooxidans ◽  
Large Scale ◽  
Low Cost ◽  
Xrd Analysis ◽  
Green Technology ◽  
Environmental Friendliness ◽  
X Ray ◽  
Pre Treatment

Arsenopyrite (FeAsS) is often associated with gold, but pre-treatment is necessary prior to gold leaching, mainly due to the gold encapsulation in the matrix of FeAsS. Bio-oxidation is attractive and promising, largely due to its simplicity, low cost and environmental friendliness. A critical problem that still impedes the large-scale applications of this green technology is its slow leaching kinetics. Some metal ions such as Ag+ have previously been found to expedite the bioleaching process. In this paper, the role of Ag+ in the arsenopyrite bioleaching by Acidithiobacillus ferrooxidans was investigated in detail by bioleaching experiments and a series of analyses including thermodynamics, X-ray diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Experimental results suggested that addition of 5 mg/L Ag+ to the leaching system could significantly improve the final As leaching efficiency from 30.4% to 47.8% and shorten the bioleaching period from 19 days to 15 days. Thermodynamic analysis indicates that Ag+ destabilises As2S2, As2S3 and S0 via forming Ag2S, which is confirmed by the XRD analysis on the phase transformation during bioleaching. SEM and XPS analyses further showed that Ag+ removed the passivating film consisting mainly of As2S2, As2S3 and S0 because Ag2S formed on the arsenopyrite surface from the start bioleaching of 36 h. In the presence of Fe3+, Ag2S could easily be dissolved to Ag+ again, likely leading to the establishment of the Ag+/Ag2S cycle. The bacteria utilised the two synergistic cycles of Fe3+/Fe2+ and Ag+/Ag2S to catalyse the bioleaching of arsenopyrite.

scholarly journals Non-Thermal Plasma-Modified Ru-Sn-Ti Catalyst for Chlorinated Volatile Organic Compound Degradation

Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1456
Author(s):  
Yujie Fu ◽  
You Zhang ◽  
Qi Xin ◽  
Zhong Zheng ◽  
Yu Zhang ◽  
...  
Keyword(s):  
Plasma Treatment ◽  
Photoelectron Spectroscopy ◽  
High Surface ◽  
High Surface Area ◽  
Surface Oxidation ◽  
Treatment Method ◽  
X Ray ◽  
Chlorinated Volatile Organic Compounds ◽  
Volatile Organic ◽  
Doped Titania

Chlorinated volatile organic compounds (CVOCs) are vital environmental concerns due to their low biodegradability and long-term persistence. Catalytic combustion technology is one of the more commonly used technologies for the treatment of CVOCs. Catalysts with high low-temperature activity, superior selectivity of non-toxic products, and resistance to chlorine poisoning are desirable. Here we adopted a plasma treatment method to synthesize a tin-doped titania loaded with ruthenium dioxide (RuO2) catalyst, possessing enhanced activity (T90%, the temperature at which 90% of dichloromethane (DCM) is decomposed, is 262 °C) compared to the catalyst prepared by the conventional calcination method. As revealed by transmission electron microscopy, X-ray diffraction, N2 adsorption, X-ray photoelectron spectroscopy, and hydrogen temperature-programmed reduction, the high surface area of the tin-doped titania catalyst and the enhanced dispersion and surface oxidation of RuO2 induced by plasma treatment were found to be the main factors determining excellent catalytic activities.

scholarly journals Performance Improvement of ZnSnO Thin-Film Transistors with Low-Temperature Self-Combustion Reaction

Electronics ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1099
Author(s):  
Ye-Ji Han ◽  
Se Hyeong Lee ◽  
So-Young Bak ◽  
Tae-Hee Han ◽  
Sangwoo Kim ◽  
...  
Keyword(s):  
Thin Film ◽  
Photoelectron Spectroscopy ◽  
Large Scale ◽  
Low Cost ◽  
Thermal Analyses ◽  
Thin Film Transistor ◽  
Sol Gel ◽  
Annealing Temperatures ◽  
Zinc Tin Oxide ◽  
Thermal Limitation

Conventional sol-gel solutions have received significant attention in thin-film transistor (TFT) manufacturing because of their advantages such as simple processing, large-scale applicability, and low cost. However, conventional sol-gel processed zinc tin oxide (ZTO) TFTs have a thermal limitation in that they require high annealing temperatures of more than 500 °C, which are incompatible with most flexible plastic substrates. In this study, to overcome the thermal limitation of conventional sol-gel processed ZTO TFTs, we demonstrated a ZTO TFT that was fabricated at low annealing temperatures of 350 °C using self-combustion. The optimized device exhibited satisfactory performance, with μsat of 4.72 cm2/V∙s, Vth of −1.28 V, SS of 0.86 V/decade, and ION/OFF of 1.70 × 106 at a low annealing temperature of 350 °C for one hour. To compare a conventional sol-gel processed ZTO TFT with the optimized device, thermogravimetric and differential thermal analyses (TG-DTA) and X-ray photoelectron spectroscopy (XPS) were implemented.

scholarly journals Synthesis of Exosome-Based Fluorescent Gold Nanoclusters for Cellular Imaging Applications

2021 ◽  
Vol 22 (9) ◽  
pp. 4433
Author(s):  
Eun Sung Lee ◽  
Byung Seok Cha ◽  
Seokjoon Kim ◽  
Ki Soo Park
Keyword(s):  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
Stokes Shift ◽  
Gold Nanoclusters ◽  
Human Colon ◽  
Cellular Imaging ◽  
Metal Nanoclusters ◽  
Human Colon Cancer ◽  
X Ray ◽  
High Concentrations

In recent years, fluorescent metal nanoclusters have been used to develop bioimaging and sensing technology. Notably, protein-templated fluorescent gold nanoclusters (AuNCs) are attracting interest due to their excellent fluorescence properties and biocompatibility. Herein, we used an exosome template to synthesize AuNCs in an eco-friendly manner that required neither harsh conditions nor toxic chemicals. Specifically, we used a neutral (pH 7) and alkaline (pH 11.5) pH to synthesize two different exosome-based AuNCs (exo-AuNCs) with independent blue and red emission. Using field-emission scanning electron microscopy, energy dispersive X-ray microanalysis, nanoparticle tracking analysis, and X-ray photoelectron spectroscopy, we demonstrated that AuNCs were successfully formed in the exosomes. Red-emitting exo-AuNCs were found to have a larger Stokes shift and a stronger fluorescence intensity than the blue-emitting exo-AuNCs. Both exo-AuNCs were compatible with MCF-7 (human breast cancer), HeLa (human cervical cancer), and HT29 (human colon cancer) cells, although blue-emitting exo-AuNCs were cytotoxic at high concentrations (≥5 mg/mL). Red-emitting exo-AuNCs successfully stained the nucleus and were compatible with membrane-staining dyes. This is the first study to use exosomes to synthesize fluorescent nanomaterials for cellular imaging applications. As exosomes are naturally produced via secretion from almost all types of cell, the proposed method could serve as a strategy for low-cost production of versatile nanomaterials.

scholarly journals Improvement of the thermal stability of dendritic silver-coated copper microparticles by surface modification based on molecular self-assembly

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Tae Hyeong Kim ◽  
Hyeji Kim ◽  
Hyo Jun Jang ◽  
Nara Lee ◽  
Kwang Hyun Nam ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Electrically Conductive ◽  
X Ray ◽  
Alkyl Chains ◽  
Conductive Film ◽  
Initial Resistance ◽  
Thermal Stability Of ◽  
Scanning Electron

AbstractIn the study reported herein, silver-coated copper (Ag/Cu) powder was modified with alkanethiols featuring alkyl chains of different lengths, namely butyl, octyl, and dodecyl, to improve its thermal stability. The modification of the Ag/Cu powders with adsorbed alkanethiols was confirmed by scanning electron microscopy with energy dispersive spectroscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis. Each powder was combined with an epoxy resin to prepare an electrically conductive film. The results confirmed that the thermal stability of the films containing alkanethiol-modified Ag/Cu powders is superior to that of the film containing untreated Ag/Cu powder. The longer the alkyl group in the alkanethiol-modified Ag/Cu powder, the higher the initial resistance of the corresponding electrically conductive film and the lower the increase in resistance induced by heat treatment.

scholarly journals Yttrium Doped TiO2 Thin Film for Gas Sensing Application Prepared by Spin Coating Method

2020 ◽  
Author(s):  
M Abdul Kaiyum ◽  
Naim Ahmed ◽  
Arif Alam ◽  
M Shamimur Rahman
Keyword(s):  
Thin Film ◽  
Photoelectron Spectroscopy ◽  
Gas Sensing ◽  
Low Cost ◽  
Pure Titanium ◽  
X Ray ◽  
Sensing Applications ◽  
Coating Method ◽  
Set Up ◽  
Spin Coater

Abstract Yttrium (Y) doped and pure Titanium Di-oxide (TiO2) thin films were prepared by using spin coater. The coater was set up in laboratory with low cost investment. The films were calcined at 450 °C for 1 hour. For characterization, Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Analysis (EDX), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Atomic Force Microscopy (AFM) were carried out. LCR Bridge - GW Instek LCR-821 was used for gas sensing applications. XPS showed that the change of electronic structure due to Y doping. SEM and AFM analysis were carried out to determine the surface morphology of the films. Yttrium (Y) decreased the crystallite size of the films and increased the surface roughness and porosity value, which was very good for many sensing applications. Gas sensing property of the deposited films were improved by the incorporation of yttrium impurities and the sensing property improved almost two times than pure TiO2 thin film. Different researches have been done their research related to this topic but no one researchers provide a precise explanation of their results, authors of this research have tried to do that. Moreover the films were prepared by a simple spin coater to reduce the production cost also.

Band alignment of HfO2/Al0.25Ga0.75N determined by x-ray photoelectron spectroscopy: Effect of SiH4 surface treatment

2014 ◽  
Vol 104 (9) ◽  
pp. 091605 ◽  
Author(s):  
Man Hon Samuel Owen ◽  
Maruf Amin Bhuiyan ◽  
Qian Zhou ◽  
Zheng Zhang ◽  
Ji Sheng Pan ◽  
...  
Keyword(s):  
Surface Treatment ◽  
Photoelectron Spectroscopy ◽  
Band Alignment ◽  
X Ray

scholarly journals Thermal Stability of Octadecyltrichlorosilane and Perfluorooctyltriethoxysilane Monolayers on SiO2

Nanomaterials ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 210
Author(s):  
Xiangdong Yang ◽  
Haitao Wang ◽  
Peng Wang ◽  
Xuxin Yang ◽  
Hongying Mao
Keyword(s):  
Thermal Stability ◽  
Thermal Behavior ◽  
Work Function ◽  
Photoelectron Spectroscopy ◽  
Vacuum Annealing ◽  
Moderate Temperature ◽  
Ultraviolet Photoelectron Spectroscopy ◽  
X Ray ◽  
Thermal Stability Of

Using in situ ultraviolet photoelectron spectroscopy (UPS) and X-ray photoelectron spectroscopy (XPS) measurements, the thermal behavior of octadecyltrichlorosilane (OTS) and 1H, 1H, 2H, and 2H-perfluorooctyltriethoxysilane (PTES) monolayers on SiO2 substrates has been investigated. OTS is thermally stable up to 573 K with vacuum annealing, whereas PTES starts decomposing at a moderate temperature between 373 K and 423 K. Vacuum annealing results in the decomposition of CF3 and CF2 species rather than desorption of the entire PTES molecule. In addition, our UPS results reveal that the work function (WF)of OTS remains the same after annealing; however WF of PTES decreases from ~5.62 eV to ~5.16 eV after annealing at 573 K.

scholarly journals Green and facile synthesis of cerium doped Ni3Fe electrocatalyst for efficient oxygen evolution reaction

2020 ◽  
Vol 34 (2) ◽  
pp. 353-363
Author(s):  
F. Kanwal ◽  
A. Batool ◽  
R. Akbar ◽  
S. Asim ◽  
M. Saleem
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Large Scale ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Three Dimensional ◽  
Alkaline Electrolyte ◽  
Hydrogen Electrode ◽  
Molar Ratios

Electrochemical water splitting is the most promising pathway to produce high-purity hydrogen to alleviate global energy crisis. This reaction demands inexpensive, efficient and robust electrocatalyst for its commercial use. Herein, we demonstrate an effective, facile and scalable method for the synthesis of cerium doped Ni3Fe nanostructures as an electrocatalyst for oxygen evolution reaction (OER) by following simple chemical bath deposition route. The different molar ratios (3, 6 and 12 mM) of cerium in the chemical bath were used to study its effect on the structural and the electrochemical properties of the Ni3Fe nanostructured films. Doping of cerium contents induced variations in the morphology of deposited Ni3Fe nanostructures. The optimized electrocatalyst Ni3Fe/Ce-6 yielded high surface area catalyst nanosheets uniformly deposited on three-dimensional conductive scaffold to ensure increase in the exposure of doped Ni3Fe catalytic sites with high electrical conductivity. As a result, this earth-abundant electrocatalyst affords high OER performance with a small overpotential of 310 mV versus reversible hydrogen electrode (RHE) at 10 mA cm-2 and retains good stability up to ~ 10 h in alkaline electrolyte. This scalable strategy has great potential in future advancement of efficient and low-cost electrocatalysts for their large-scale application in energy conversion systems.                     KEY WORDS: Oxygen evolution, Electrocatalyst, Ni3Fe nanostructures, Cerium, Alkaline electrolyte   Bull. Chem. Soc. Ethiop. 2020, 34(2), 353-363 DOI: https://dx.doi.org/10.4314/bcse.v34i2.12

scholarly journals Nanosheets of CuCo2O4 As a High-Performance Electrocatalyst in Urea Oxidation

2019 ◽  
Vol 9 (4) ◽  
pp. 793 ◽  
Author(s):  
Camila Zequine ◽  
Fangzhou Wang ◽  
Xianglin Li ◽  
Deepa Guragain ◽  
S.R. Mishra ◽  
...  
Keyword(s):  
Fuel Cells ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Nickel Foam ◽  
Low Cost ◽  
Agricultural Waste ◽  
Bifunctional Catalyst ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electroactive Material

The urea oxidation reaction (UOR) is a possible solution to solve the world’s energy crisis. Fuel cells have been used in the UOR to generate hydrogen with a lower potential compared to water splitting, decreasing the costs of energy production. Urea is abundantly present in agricultural waste and in industrial and human wastewater. Besides generating hydrogen, this reaction provides a pathway to eliminate urea, which is a hazard in the environment and to people’s health. In this study, nanosheets of CuCo2O4 grown on nickel foam were synthesized as an electrocatalyst for urea oxidation to generate hydrogen as a green fuel. The synthesized electrocatalyst was characterized using X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. The electroactivity of CuCo2O4 towards the oxidation of urea in alkaline solution was evaluated using electrochemical measurements. Nanosheets of CuCo2O4 grown on nickel foam required the potential of 1.36 V in 1 M KOH with 0.33 M urea to deliver a current density of 10 mA/cm2. The CuCo2O4 electrode was electrochemically stable for over 15 h of continuous measurements. The high catalytic activities for the hydrogen evolution reaction make the CuCo2O4 electrode a bifunctional catalyst and a promising electroactive material for hydrogen production. The two-electrode electrolyzer demanded a potential of 1.45 V, which was 260 mV less than that for the urea-free counterpart. Our study suggests that the CuCo2O4 electrode can be a promising material as an efficient UOR catalyst for fuel cells to generate hydrogen at a low cost.

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