Friction Behavior of Silver Perrhenate in Oil as Lubricating Additive for Use at Elevated Temperatures

In this study, we use an aqueous solution synthesis method to prepare silver perrhenate powders and suspend them into a poly alpha olefin (PAO) base oil with polyoxyethylene octylphenyl ether. Four ball tests and ball-on-disk reciprocating mode are performed to determine how silver perrhenate performs tribologically as a lubricating additive over a wide range of temperatures. The physical and chemical properties, as well as the lubricating mechanisms of the silver perrhenate additive, are characterized via X-ray diffraction, scanning electron microscope, Fourier transformation infrared spectroscopy, Raman spectrum, and X-ray photoelectron spectroscopy. The four-ball test results demonstrate that the oil added with silver perrhenate additive is more effective than the base oil in reducing friction and improving wear resistance, and provides the best lubricating performance when at a concentration of 0.5 wt%. The reciprocating mode findings indicate that the hybrid lubricant exhibits distinctively better tribological properties than the base oil at high temperatures, and its low shear strength and chemical inertness allow for low friction at elevated temperatures. The resulting silver perrhenate layer that incorporates native superalloy oxides on the worn surface can provide lubrication by serving as a barrier that prevents direct contact between the rubbing surfaces at elevated temperatures.

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Ultra-low wear and anti-oxidation properties of microcrystalline graphite oxide-magnesium silicate hydroxide composite nanoadditives in the poly-alpha-olefin base oil

Journal of Tribology ◽

10.1115/1.4051200 ◽

2021 ◽

pp. 1-23

Author(s):

Wang Kai ◽

Qiuying Chang ◽

Rongqin Gao

Keyword(s):

Graphite Oxide ◽

Photoelectron Spectroscopy ◽

Hydrothermal Process ◽

Magnesium Silicate ◽

Wear Scar ◽

Wear Properties ◽

Wear Scar Diameter ◽

Base Oil ◽

X Ray ◽

Alpha Olefin

Abstract Graphite-based materials and hydrothermal synthetic magnesium silicate hydroxide (MSH) had shown outstanding performances as lubricant additives. In this paper, microcrystalline graphite oxide-magnesium silicate hydroxide (MGO-MSH) composite additives using pre-oxidized MGO as one of the precursors were prepared at a mild hydration condition, and their tribological properties in poly-alpha-olefin oil (PAO 10) were demonstrated by a four-ball tester. The tribological results showed that the optimal concentration of MGO-MSH in oil was 0.3 wt% under 600 N, 600 rpm. Meanwhile, the average wear scar diameter of the ball samples tested in composite-suspending oil was reduced by 36.3% compared with that obtained by pure PAO 10. By means of scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Raman spectra, and X-ray photoelectron spectroscopy (XPS), it was verified that MGO was involved in the synthesis of MSH, and MSH was anchored on MGO during the hydrothermal process. In addition, it was confirmed that carbon-containing tribo-film was formed on the smooth wear region of the wear scar, and was of excellent anti-oxidation wear properties.

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Development of a nitrogen-doped 2D material for tribological applications in the boundary-lubrication regime

Beilstein Journal of Nanotechnology ◽

10.3762/bjnano.8.147 ◽

2017 ◽

Vol 8 ◽

pp. 1476-1483 ◽

Cited By ~ 13

Author(s):

Shende Rashmi Chandrabhan ◽

Velayudhanpillai Jayan ◽

Somendra Singh Parihar ◽

Sundara Ramaprabhu

Keyword(s):

Electron Microscopy ◽

Tribological Properties ◽

Photoelectron Spectroscopy ◽

Large Scale ◽

Synthesis Method ◽

Field Trials ◽

Base Oil ◽

X Ray ◽

Nitrogen Doped ◽

Sliding Mechanism

The present paper describes a facile synthesis method for nitrogen-doped reduced graphene oxide (N-rGO) and the application of N-rGO as an effective additive for improving the tribological properties of base oil. N-rGO has been characterized by different characterization techniques such as X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and Raman spectroscopy. N-rGO-based nanolubricants are prepared and their tribological properties are studied using a four-ball tester. The nanolubricants show excellent stability over a period of six months and a significant decrease in coefficient of friction (25%) for small amounts of N-rGO (3 mg/L). The improvement in tribological properties can be attributed to the sliding mechanism of N-rGO accompanied by the high mechanical strength of graphene. Further, the nanolubricant is prepared at large scale (700 liter) and field trials are carried out at one NTPC thermal plant in India. The implementation of the nanolubricant in an induced draft (ID) fan results in the remarkable decrease in the power consumption.

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Facile Preparation of Carbon Nitride-ZnO Hybrid Adsorbent for CO2 Capture: The Significant Role of Amine Source to Metal Oxide Ratio

Catalysts ◽

10.3390/catal11101253 ◽

2021 ◽

Vol 11 (10) ◽

pp. 1253

Author(s):

Siti Aishah Anuar ◽

Khairul Naim Ahmad ◽

Ahmed Al-Amiery ◽

Mohd Shahbudin Masdar ◽

Wan Nor Roslam Wan Isahak

Keyword(s):

Electron Microscopy ◽

Metal Oxide ◽

Photoelectron Spectroscopy ◽

Physical Adsorption ◽

Synthesis Method ◽

Chemical Properties ◽

Gaseous Fuel ◽

X Ray ◽

Transmission Electron ◽

Adsorption Analysis

The presence of CO2 in gaseous fuel and feedstock stream of chemical reaction was always considered undesirable. High CO2 content will decrease quality and heating value of gaseous fuel, such as biohydrogen, which needs a practical approach to remove it. Thus, this work aims to introduce the first C3N4-metal oxide hybrid for the CO2 cleaning application from a mixture of CO2-H2 gas. The samples were tested for their chemical and physical properties, using field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), physical adsorption analysis (BET), fourier-transform infrared (FTIR), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The CO2 capacity test was carried out by means of a breakthrough test at 1 atm and 25° C using air as a desorption system. Among the samples, amine/metal oxide mass ratio of 2:1 (CNHP500-2(2-1)) showed the best performance of 26.9 wt. % (6.11 mmol/g), with a stable capacity over 6 consecutive cycles. The hybrid sample also showed 3 times better performance than the raw C3N4. In addition, it was observed that the hydrothermal C3N4 synthesis method demonstrated improved chemical properties and adsorption performance than the conventional dry pyrolysis method. In summary, the performance of hybrid samples depends on the different interactive factors of surface area, pore size and distribution, basicity, concentration of amine precursors, ratio of amines precursors to metal oxide, and framework stability.

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Efficient Adsorption of Methylene Blue by Porous Biochar Derived from Soybean Dreg Using a One-Pot Synthesis Method

Molecules ◽

10.3390/molecules26030661 ◽

2021 ◽

Vol 26 (3) ◽

pp. 661

Author(s):

Zhiwei Ying ◽

Xinwei Chen ◽

He Li ◽

Xinqi Liu ◽

Chi Zhang ◽

...

Keyword(s):

Electron Microscopy ◽

Methylene Blue ◽

Photoelectron Spectroscopy ◽

Synthesis Method ◽

Urban Pollution ◽

Maximum Adsorption Capacity ◽

One Pot ◽

Average Pore ◽

X Ray ◽

Isotherm Equation

Soybean dreg is a by-product of soybean products production, with a large consumption in China. Low utilization value leads to random discarding, which is one of the important sources of urban pollution. In this work, porous biochar was synthesized using a one-pot method and potassium bicarbonate (KHCO3) with low-cost soybean dreg (SD) powder as the carbon precursor to investigating the adsorption of methylene blue (MB). The prepared samples were characterized with scanning electron microscopy (SEM), transmission electron microscopy (TEM), elemental analyzer (EA), Brunauer-Emmett-Teller (BET), X-ray diffractometer (XRD), Raman spectroscopy (Raman), Fourier transform infrared spectrometer (FTIR), and X-ray photoelectron spectroscopy (XPS). The obtained SDB-K-3 showed a high specific surface area of 1620 m2 g−1, a large pore volume of 0.7509 cm3 g−1, and an average pore diameter of 1.859 nm. The results indicated that the maximum adsorption capacity of SDB-K-3 to MB could reach 1273.51 mg g−1 at 318 K. The kinetic data were most consistent with the pseudo-second-order model and the adsorption behavior was more suitable for the Langmuir isotherm equation. This study demonstrated that the porous biochar adsorbent can be prepared from soybean dreg by high value utilization, and it could hold significant potential for dye wastewater treatment in the future.

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Synthesis of Ce1−xPdxO2−δ Solid Solution in Molten Nitrate

Catalysts ◽

10.3390/catal10060640 ◽

2020 ◽

Vol 10 (6) ◽

pp. 640

Author(s):

Hideaki Sasaki ◽

Keisuke Sakamoto ◽

Masami Mori ◽

Tatsuaki Sakamoto

Keyword(s):

Electron Microscopy ◽

Solid Solution ◽

Solid Solutions ◽

Photoelectron Spectroscopy ◽

Synthesis Method ◽

X Ray Diffraction ◽

X Ray ◽

Transmission Electron ◽

Co Precipitation ◽

Ionic States

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.

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A Highly Sensitive Room Temperature CO2 Gas Sensor Based on SnO2-rGO Hybrid Composite

Materials ◽

10.3390/ma14030522 ◽

2021 ◽

Vol 14 (3) ◽

pp. 522

Author(s):

Zhi Yan Lee ◽

Huzein Fahmi bin Hawari ◽

Gunawan Witjaksono bin Djaswadi ◽

Kamarulzaman Kamarudin

Keyword(s):

Electron Microscopy ◽

Carbon Dioxide ◽

Gas Sensor ◽

Photoelectron Spectroscopy ◽

Hybrid Composite ◽

Room Temperature ◽

Co2 Gas ◽

X Ray ◽

Wide Range ◽

Co2 Gas Sensor

A tin oxide (SnO2) and reduced graphene oxide (rGO) hybrid composite gas sensor for high-performance carbon dioxide (CO2) gas detection at room temperature was studied. Since it can be used independently from a heater, it emerges as a promising candidate for reducing the complexity of device circuitry, packaging size, and fabrication cost; furthermore, it favors integration into portable devices with a low energy density battery. In this study, SnO2-rGO was prepared via an in-situ chemical reduction route. Dedicated material characterization techniques including field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), energy dispersive X-ray (EDX) spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) were conducted. The gas sensor based on the synthesized hybrid composite was successfully tested over a wide range of carbon dioxide concentrations where it exhibited excellent response magnitudes, good linearity, and low detection limit. The synergistic effect can explain the obtained hybrid gas sensor’s prominent sensing properties between SnO2 and rGO that provide excellent charge transport capability and an abundance of sensing sites.

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Nano-PAA-CuCl2 Composite as Fenton-Like Reusable Catalyst to Enhanced Degrade Organic Pollutant MB/MO

Catalysts ◽

10.3390/catal11010010 ◽

2020 ◽

Vol 11 (1) ◽

pp. 10

Author(s):

Yang Dang ◽

Yu Cheng ◽

Yukun Zhou ◽

Yifei Huang ◽

Kaige Wang

Keyword(s):

Photoelectron Spectroscopy ◽

Self Assembly ◽

Organic Pollutant ◽

Energy Dispersive Spectrometer ◽

Chemical Properties ◽

Anodic Alumina ◽

Alumina Substrate ◽

Reusable Catalyst ◽

X Ray ◽

Nanoporous Anodic Alumina

The treatment of organic dye contaminants in wastewaters has now becoming more imperative. Fenton-like degradation of methylene blue (MB) and methyl orange (MO) in aqueous solution was investigated by using a nanostructure that a layer of CuCl2 nanoflake film grown on the top surface of nanoporus anodic alumina substrate (nano-PAA-CuCl2) as catalyst. The new nano-PAA-CuCl2 composite was fabricated with self-assembly approach, that is, a network porous structure film composed of CuCl2 nanoflake grown on the upper surface of nanoporous anodic alumina substrate, and the physical and chemical properties are characterized systematically with the X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and high-resolution transmission electron microscopy (HRTEM), Energy Dispersive Spectrometer (EDS), X-ray photoelectron spectroscopy (XPS). The experimental results showed that the nano-PAA-CuCl2 catalyst presented excellent properties for the degradation of two typical organic pollutants such as MB and MO, which were almost completely degraded with 8 × 10−4mol/L nano-PAA-CuCl2 catalyst after 46 min and 60 min at reaction conditions of H2O2 18 mM and 23 mM, respectively. The effects of different reaction parameters such as initial pH, H2O2 concentration, catalyst morphology and temperature were attentively studied. And more, the stability and reusability of nano-PAA-CuCl2 were examined. Finally, the mechanism of MB and MO degradation by the nano-PAA-CuCl2/H2O2 system was proposed, based on the experimental data of the BCA and the temperature-programmed reduction (H2-TPR) and theoretical analysis, the reaction kinetics belonged to the pseudo-first-order equation. This new nanoporous composite material and preparation technology, as well as its application in Fenton-like reaction, provide an effective alternative method with practical application significance for wastewater treatment.

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Oxidation of Alloy-X in Subcritical, Transition, and Supercritical Water

CORROSION ◽

10.5006/3881 ◽

2021 ◽

Author(s):

Zachary Karmiol ◽

Dev Chidambaram

Keyword(s):

Supercritical Water ◽

Photoelectron Spectroscopy ◽

Focused Ion Beam ◽

Elevated Temperatures ◽

Subcritical Water ◽

Ion Beam ◽

X Ray Diffraction ◽

X Ray ◽

Nickel Based Superalloy ◽

Before And After

This work investigates the oxidation of a nickel based superalloy, namely Alloy X, in water at elevated temperatures: subcritical water at 261°C and 27 MPa, the transition between subcritical and supercritical water at 374°C and 27 MPa, and supercritical water at 380°C and 27 MPa for 100 hours. The morphology of the sample surfaces were studied using scanning electron microscopy coupled with focused ion beam milling, and the surface chemistry was investigated using X-ray diffraction, Raman spectroscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy before and after exposure studies. Surfaces of all samples were identified to comprise of a ferrite spinel containing aluminum.

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The effect of cobalt on morphology, structure, and ORR activity of electrospun carbon fibre mats in aqueous alkaline environments

Beilstein Journal of Nanotechnology ◽

10.3762/bjnano.12.87 ◽

2021 ◽

Vol 12 ◽

pp. 1173-1186

Author(s):

Markus Gehring ◽

Tobias Kutsch ◽

Osmane Camara ◽

Alexandre Merlen ◽

Hermann Tempel ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Inductively Coupled Plasma ◽

Elevated Temperatures ◽

Current Collector ◽

Alkaline Media ◽

Emission Spectrometry ◽

Free Standing ◽

X Ray ◽

Turbostratic Carbon ◽

Current Densities

An innovative approach for the design of air electrodes for metal–air batteries are free-standing scaffolds made of electrospun polyacrylonitrile fibres. In this study, cobalt-decorated fibres are prepared, and the influence of carbonisation temperature on the resulting particle decoration, as well as on fibre structure and morphology is discussed. Scanning electron microscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, elemental analysis, and inductively coupled plasma optical emission spectrometry are used for characterisation. The modified fibre system is compared to a benchmark system without cobalt additives. Cobalt is known to catalyse the formation of graphite in carbonaceous materials at elevated temperatures. As a result of cobalt migration in the material the resulting overall morphology is that of turbostratic carbon. Nitrogen removal and nitrogen-type distribution are enhanced by the cobalt additives. At lower carbonisation temperatures cobalt is distributed over the surface of the fibres, whereas at high carbonisation temperatures it forms particles with diameters up to 300 nm. Free-standing, current-collector-free electrodes assembled from carbonised cobalt-decorated fibre mats display promising performance for the oxygen reduction reaction in aqueous alkaline media. High current densities at an overpotential of 100 mV and low overpotentials at current densities of 333 μA·cm−2 were found for all electrodes made from cobalt-decorated fibre mats carbonised at temperatures between 800 and 1000 °C.

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Graphitic Nitrogen in Carbon Catalysts Important for the Reduction of Nitrite Revealed by 15N NMR Spectroscopy at Natural Abundance

10.26434/chemrxiv.12906227.v1 ◽

2020 ◽

Author(s):

Zheng Chen ◽

Aleksander Jaworski ◽

Jianhong Chen ◽

Tetyana Budnyak ◽

Ireneusz Szewczyk ◽

...

Keyword(s):

Electron Microscopy ◽

Photoelectron Spectroscopy ◽

Reduction Reaction ◽

Nitrite Reduction ◽

15N Nmr ◽

Carbon Catalyst ◽

X Ray ◽

Wide Range ◽

Alkaline Conditions

Metal-free nitrogen-doped carbon is considered as a green functional material, but the structural determination of the atomic positions of nitrogen remains challenging. We recently demonstrated that directly-excited solid state 15N NMR (ssNMR) spectroscopy is a powerful tool for the determination of such positions in an N-doped carbon at natural 15N isotope abundance. Here we present a green chemistry approach to the synthesis of N-doped carbon using cellulose as precursor, and a study of the catalytic properties and atomic structures of the related catalyst. The N-doped carbon (NH3) was obtained by oxidation of cellulose with HNO3 followed by ammonolysis at 800°C. It had a N content of 6.5 wt.% and a surface area of 557 m2 g–1, and 15N ssNMR spectroscopy provided evidence for graphitic nitrogen besides of regular pyrrolic and pyridinic nitrogen. This structure determination enabled probing the role of graphitic nitrogen for electrocatalytic reactions, such as the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and nitrite reduction reaction. The N-doped carbon catalyst (NH3) had higher electrocatalytic activities in OER and HER under alkaline conditions and a higher activity for nitrite reduction, as compared with a catalyst prepared by carbonization of the HNO3-treated cellulose in N2. The electrocatalytic selectivity for nitrite reduction of the N-doped carbon catalyst (NH3) was directly related to the graphitic nitrogen functions. Complementary structural analysis by means of 13C and 1H ssNMR, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and low-temperature N2 adsorption were preformed and provided support to the findings. The results show that directly-excited 15N ssNMR at natural 15N abundance is generally capable to provide information on N-doped carbon materials, and it is expected that the approach can be applied to a wide range of solids with an intermediate amount of N atoms.

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