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Title: Mechanism and kinetics of carbide dissolution in near alpha Ti-5.6Al-4.8Sn-2Zr-1Mo-0.35Si-0.7Nd titanium alloy

Journal Article · · Materials Characterization
 [1];  [2]
  1. School of Environmental and Materials Engineering, Yantai University, 32 Qingquan Road, Yantai 264005 (China)
  2. Titanium Alloy Laboratory, Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang 110016 (China)

The present work evaluates the influence of bulk carbon content and aging temperature on the stability of carbide in near alpha Ti-5.6Al-4.8Sn-2Zr-1Mo-0.35Si-0.7Nd titanium alloy. The carbide particles were formed during heat treatment in the {beta} phase field and preserved by water quenching. Subsequent aging treatments at 750-850 Degree-Sign C caused partial dissolution of these precipitates, as a result of the peritectoid reaction between the {beta} phase and carbide. The models based on interface reaction controlled dissolution, via uniform atomic detachment, dislocation mechanism or vacancy flow, yielded experimental predictions comparable to the observed dissolution kinetics. Furnace cooling after heat treatment in the {beta} phase field dissolved carbide particles completely, and the microstructure changed from acicular-like or block {alpha} to equiaxed {alpha} with increase of carbon content. - Highlights: Black-Right-Pointing-Pointer Carbide dissolution occurs at precipitate/matrix interfaces, forming {beta}-depleted zone. Black-Right-Pointing-Pointer Peritectoid reaction is responsible for drastic reduction of carbide volume fraction. Black-Right-Pointing-Pointer Slower dissolution rate is accounted by dislocation, vacancy flow, and curvature. Black-Right-Pointing-Pointer Lamellar changed to equiaxed {alpha} with increasing carbon from {beta} furnace cooling.

OSTI ID:
22066398
Journal Information:
Materials Characterization, Vol. 62, Issue 12; Other Information: Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 1044-5803
Country of Publication:
United States
Language:
English