Hypothesis: Carbon microspheres have been shown to reduce friction and surface wear at relatively low speeds and high applied loads (i.e., within the boundary lubrication regime). We hypothesize that in dilute colloidal lubricating systems there is an interplay between the size of the carbon microspheres and the lubrication gap size, which determines the dominant lubricating mechanism of the system.
Experiments: A 60 wt% aqueous glycerol solution was used as the base lubricant and compared to various carbon particle-based lubricant formulations ranging in particle concentrations from 0.05 to 0.30 vol%. The tribological properties of the various lubricant formulations were tested on a pin-on-disk tribometer. A simplified Stribeck plot was produced to understand the changing mechanism of lubrication over a wide range of conditions.
Findings: The Stribeck curves show that the carbon microspheres assist lubrication by a rolling mechanism primarily in the boundary lubrication regime. A 0.20 vol% carbon-based lubricant formulation showed the best friction reduction compared to the base lubricant. Increasing speed increases the lubricating gap between the friction pair beyond the size of the particles, thereby nullifying the rolling mechanism of the particles. We introduce a modified specific film thickness parameter to determine the lubrication regime in a particle-lubricant system.
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http://dx.doi.org/10.1016/j.jcis.2023.07.089 | DOI Listing |
Sci Rep
December 2024
Shandong Engineering Research Center of Green and High-value Marine Fine Chemical, Weifang University of Science and Technology, Shouguang, 262700, People's Republic of China.
To enhance the volumetric energy density and initial coulombic efficiency (ICE) of titanium oxide (TiO) as anode electrode material for lithium-ion batteries (LIB), this study employed a surface-confined in-situ inter-growth mechanism to prepare a TiO embedded carbon microsphere composite. The results revealed that the composite exhibited a highly integrated structure of TiO with oxygen vacancies and carbon, along with an exceptionally small specific surface area of 11.52 m/g.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, P. R. China.
Developing hybrid fluorescence (FL)/room-temperature phosphorescent (RTP) materials in dry-state, aqueous, and organic solvents holds paramount importance in broadening their applications. However, it is extremely challenging due to dissolved oxygen and solvent-assisted relaxation causing RTP quenching in an aqueous environment and great dependence on SiO-based materials. Herein, an efficient endogenetic carbon dot (CD) strategy within melamine-formaldehyde (MF) microspheres to activate RTP of CDs has been proposed through the pyrolysis of isophthalic acid (IPA) molecules and branched-chain intra-microspheres.
View Article and Find Full Text PDFNanoscale
December 2024
Key Laboratory of Advanced Energy Storage and Conversion of Wenzhou, Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, P. R. China.
Lead oxides (PbO, 1 ≤ ≤ 2) are promising high-capacity and low-cost anodes for lithium ion batteries (LIBs). However, the huge lithiation-induced volume expansion of conventional large-sized PbO particles leads to severe electrode pulverization with poor cycling stability. Herein, a rare mixed-valence PbO with a unique hierarchical architecture of nanoparticle-assembled interconnected hollow spheres (denoted PbO NAHSs) is crafted by introducing polyvinylpyrrolidone (PVP) into the solution of generating β-PbO microspheres (MSs), which is exploited for the first time as a potential advanced anode material for LIBs.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
December 2024
Department of Organic Chemistry, Faculty of Chemistry, Alzahra University, Tehran, Iran.
The efficient utilization of light and the prolonged lifetime of photo-induced charge carriers are essential elements that contribute to superior photocatalytic activity. Yolk-shell nanostructures with porous shells and mobile cores offer significant structural advantages in achieving these goals. However, designing yolk-shell multicomponent nanocomposites with diverse architectures remains a persistent challenge.
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