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Kinetic study of low-temperature transient liquid phase joining of an aluminum-sic composite

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Abstract

The transient liquid phase (TLP) joining of an aluminum 6061-SiC composite using a gallium interface has been investigated. The observed kinetics of this process suggest that diffusion occurs along interphase and subgrain boundaries at low temperatures (<723 K). An existing TLP model has been modified to account for this behavior.

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Abbreviations

C :

binary solute concentration

C β :

solute concentration in original predeposited film

t :

time coordinate

Dl, Ds:

solute diffusivity in liquid and solid

h o :

half-thickness of original predeposited solute film

ξ :

position of solid/liquid interface (x direction)

γ :

growth constant

C :

solute concentration at α liquidus

C αl :

solute concentration at α solidus

D app :

apparent solute diffusivity

h exp :

location of experimentally observed slope change on semilog plots

h,theo:

location of theoretically predicted slope change on semilog plots

τ :

liquid residence time

σ :

thickness of liquid film at grain boundaries

x, y :

Cartesian coordinates

h 1 h 2 :

maximum penetration distance (x direction)

h 3 :

for stages 1 through 3

t1, t2, t3:

time required to complete stages 1 through 3

X l :

volume fraction of liquid phase

I :

excess solute content

Jx, Jy:

flux of solute inx andy directions

D :

interdiffusion coefficient┐

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Sabathier, V., Edwards, G.R. & Cross, C.E. Kinetic study of low-temperature transient liquid phase joining of an aluminum-sic composite. Metall Mater Trans A 25, 2705–2714 (1994). https://doi.org/10.1007/BF02649223

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