Solidification Flashcards

1
Q

What do grain boundaries do to material strength?

A

Increase strength at low temperatures, decrease strength at high temps (as they deform first)

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2
Q

What is the driving force for nucleation and how is it calculated?

A

Free energy reduction caused by solidification, calculated by the difference between liquid and solidus lines
ΔGv = ΔHv.ΔT/Tm
Gv = Gibbs energy per volume, Hv 0 enthalpy per volume
Only true for pure alloys (used as estimate for others)

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3
Q

What is undercooling?

A

When a substance is cooled below a transformation temperature without transforming (in a meta-stable state)

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4
Q

What’s the free energy change caused by nucleation?

A
ΔGr = Vs.ΔGv + A.Ysl
Gr = free energy change, Vs = nucleus volume, Gv = free energy difference of solidification per volume, A = area, Ysl = solid/liquid interface energy
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5
Q

What is meant by the critical radius?

A

On a ΔG vs r curve, VsΔGv and A.Ysl are plotted, product of them plotted, r* = peak of this product = when increasing nucleated particle is energetically favourable
Below r* energetically favourable p decrease nucleation, above r* energetically favourable to increase nucleation

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6
Q

Define the energy barrier

A

This is the minimum energy required to nucleate, this is the corresponding G value for r* on the ΔG vs r graph

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7
Q

How is the probability of clusters forming with a certain radius calculated?

A
P(r) = e^(-ΔGr/KT)
Gr = free energy change upon nucleation, k = Boltzmann constant,T = temp, P(r) is the probability of clusters forming with radius r
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8
Q

What is the maximum cluster size?

A

r* is the maximum cluster size because smaller radii are more likely to spontaneously form (require less atoms to collide)

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9
Q

Explain critical undercooling

A

Nucleation barrier drops with increased undercooling which means probability of getting nuclei with a critical radius is 0 until a critical degree of undercooling has occurred

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10
Q

What is heterogenous nucleation?

A

An already existing interface acts as a nucleation point = lower nucleation barrier = more likely nucleation, r* is unaffected, once nucleation has occurred atoms are added like normal for the nucleation point to grow

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11
Q

What is the wetting angle?

A

Wetting angle is how much an interface reduces the nucleation barrier by, a small wetting angle = large reduction

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12
Q

Explain the effects of dendritic solidification

A
Solubility is lower in solid than in liquid = As interface moves it rejects alloying elements = enriched liquid 
K = Cs/Cl 
Partition coefficient (dictates how much solid is rejected) = comp of solid/comp of liquid
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13
Q

What’s the difference between global and local equilibrium?

A

Global - phase fractions and comp follow phase diagram, G always at minimum, no temp or comp gradients
Local - variation in comp and temp, level rule not follow, phase diagram only followed at interface

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14
Q

What is meant by constitutional undercooling?

A

Cooling of liquid below solidification temp, means dendrites form as small fluctuations at the interface result in larger driving forces = dendritic growth

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15
Q

When does dendritic growth occur?

A

Can only occur when an alloy
When cooling > diffusion
When G/V < To/Dl
G = temp gradient, V = interface velocity, To = Temp L - Temp S, Dl = diffusion in liquid
When G/V > To/Dl then planar interfacial growth occurs

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16
Q

What is equiaxed solidification?

A

Accelerated growth as surrounding liquid always undercooled = fast dendritic growth

17
Q

Why can’t dendrites grow in pure metals?

A

No chemical differences = dendritic structure can’t be seen

18
Q

Draw a dendritic structure and label

A

Dendrites have a parabolic tip as inc SA:volume = faster solidification (easiest or eject solute)
Primary, secondary and tertiary arms in direction of solidification, PDAS and SDAS

19
Q

What happens when cooling > diffusion rate?

A

Expelled solute can’t diffuse away = different comp of liquid = follows different part of phase diagram, when comp = eutectic comp then rest of liquid follows eutectic reaction
Means solid has enriched outer layers (layer that solidifies last) = segregation = diff material properties throughout structure = incipient melting could occur (some melts first)

20
Q

What happens when diffusion rate > cooling rate

A

Phase diagram is followed as liquid always in equilibrium as solute can diffuse away