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Volume fraction

About: Volume fraction is a research topic. Over the lifetime, 16312 publications have been published within this topic receiving 374181 citations.


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Journal ArticleDOI
TL;DR: In this paper, BN particles fabricated with different surface treatments were used to prepare thermally conductive polymer composites by epoxy wetting, and the results indicate that surface-curing agents interrupt the interaction between the filler and matrix, and do not always enhance thermal conductivity.

94 citations

Journal ArticleDOI
TL;DR: In this paper, an analytical model that accounts for the different variation of the limiting grain radius with volume fraction of particles found in previous computer simulations as compared to the classic Zener predictions is presented.

93 citations

Journal ArticleDOI
TL;DR: In this article, a new gelcasting system based on aqueous-based alumina-poly(vinyl alcohol) (PVA) suspensions cross-linked by an organotitanate coupling agent has been developed.
Abstract: A new gelcasting system based on aqueous-based alumina-poly(vinyl alcohol) (PVA) suspensions cross-linked by an organotitanate coupling agent has been developed. The chemorheological properties of this system exhibited a strong compositional dependence. A sol-gel phase diagram was established, which yielded the critical titanium concentration ([Ti]c) required for gelation at a given PVA volume fraction as well as the minimum PVA volume fraction (φminPVA= 0.0245) and titanium concentration ([Ti]min= 9.984 × 10-4 g of Ti/mL) below which gelation was not observed irrespective of solution composition. The gelation time of suspensions of constant PVA volume fraction (φsolnPVA) decreased with increased cross-linking agent concentration, temperature, and solids volume fraction. The steady-state viscosity and elastic modulus of polymer solutions (φsolnPVA= 0.05) of varying [Ti] were well described by the percolation model, giving scaling exponents of 0.84 and 1.79, respectively. The steady-state elastic modulus of gelcasting suspensions, which provided a measure of their handling strength in the as-gelled state, increased with increased solids volume fraction.

93 citations

Journal ArticleDOI
TL;DR: In this article, the changes in the microstructure and wear resistance of a powder metallurgical high-Cr white iron after the incorporation of TiC particles were studied in the present work.
Abstract: The changes in the microstructure and wear resistance of a powder metallurgical high-Cr white iron after the incorporation of TiC particles were studied in the present work. Various reinforcement volume fractions and sizes were used in order to examine their influence on the three-body abrasion wear resistance. The experiments were carried out at three different austenitizing temperatures. The most important observation after a microstructural examination was the increased amount of martensite in the composites subjected to identical heat treatment procedures with the unreinforced alloy. The austenite-to-martensite transformation in the composites increased with the TiC volume fraction and with the austenitizing temperature. This indicates that the two parameters have a key role in the transformation mechanism, which seems to be mechanically induced. The increasing of martensitic transformation with the TiC content in the composites enhanced continuously the supporting ability of the iron alloy matrix to the TiC particles, which in turn increased the wear resistance of the composites. The abrasion wear resistance increased with the TiC volume fraction until the onset of spalling. However, in composites containing coarse reinforcements, spalling occurred earlier in the wear process. This decreased wear resistance significantly because spalled TiC particles contributed additionally to wear.

93 citations

Journal ArticleDOI
TL;DR: In this paper, phase field simulations of grain growth in three-dimensional polycrystalline systems containing finely dispersed second-phase particles were executed with various volume fractions of the secondphase particles.

93 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023965
20222,020
2021744
2020736
2019786
2018696