Hi allWhy does a molten metal solidify with decrease in

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Discussion Overview

The discussion revolves around the phenomenon of molten metals solidifying upon cooling, specifically exploring the reasons behind the stability of closed-packed structures compared to amorphous liquid states. Participants delve into concepts of free energy, nucleation, and the conditions under which solidification occurs, including the role of impurities and supercooling.

Discussion Character

  • Exploratory
  • Technical explanation
  • Conceptual clarification
  • Debate/contested

Main Points Raised

  • Some participants question why molten metals solidify at specific temperatures and whether they can remain in a liquid state below the melting point.
  • Others explain that solidification is driven by a decrease in free energy when a liquid is supercooled, referencing the role of nucleation and impurities in this process.
  • A participant cites a textbook that discusses the relationship between free energy, enthalpy, and entropy during phase transformations, emphasizing that solidification is energetically favorable when the liquid is undercooled.
  • There are discussions about the critical radius for nucleation and how it influences the solidification process, with mathematical formulations provided to illustrate these concepts.
  • Some participants propose that the stability of solids is linked to higher bond density compared to liquids, suggesting that this contributes to lower free energy states.
  • Questions arise regarding the nature of the heat of fusion and how excess energy is stored in the liquid state, with references to the potential energy associated with atomic separation.
  • There is acknowledgment that not all metals adopt face-centered cubic (FCC) or hexagonal close-packed (HCP) structures, with electronic structure being a contributing factor.
  • One participant notes that while crystallinity is a common state for metals, it is not the only form of solid, and the discussion touches on the broader implications of solid-state physics and bonding theories.

Areas of Agreement / Disagreement

Participants express various viewpoints on the mechanisms of solidification and the factors influencing free energy, indicating that multiple competing views remain. The discussion does not reach a consensus on the specific reasons for the stability of solid states over liquid states.

Contextual Notes

Limitations in understanding arise from the complexity of phase transformations and the dependence on specific conditions such as temperature, impurities, and atomic structure. The discussion highlights the nuanced nature of free energy contributions from enthalpy and entropy without resolving these complexities.

pukb
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Hi all

Why does a molten metal solidify with decrease in temperature. or in other words why is a closed packed structure more stable than an amorphous liquid melt. I have read that the free energy below melting point is lesser for solid state than that of for liquid state at the same temperature.But the question that is troubling me is why is free energy in solid state lesser?
 
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Liquid to solid. Most elements do this, but at different temperatures.

Solids tend to form along crystalline planes.

To make amorphous materials, particularly in metals, usually requires rapid solidification. Metal oxides would more readily form amorphous compounds, particularly where different cation species are involved.
 


But the question is exactly that. Why does it solidify at certain temperatures?
Cant it remain in liquid phase below melting point?
 


Supercooling liquids is possible. Water can be cooled to about 253K without it freezing but it has to be clean water free of impurities. A liquid freezes becuase it nucleates at a point. Nucleation occurs due to impurities, surface texture of container e.t.c and it becomes energetically favourable to change state.

A good treatment of this is in "Phase Transformations of Metals and Alloys" by Porter and Eastling.
 


Page 10 of this book desribe this.

"In dealing with pahse transformations we are often concerned with the difference in free energy between two phases at temperatures away from the equilibrium temperature. For example, if a liquid is undercooled by a ΔT below T[itex]_{m}[/itex] beofre it solidifies, solidification will be accompanied by a decrease in free energy [itex]\Delta[/itex]G. This free energy decrease provised the driving force for solidification"

At temp T

[itex]\Delta[/itex]G = [itex]\Delta[/itex]H -T[itex]\Delta[/itex]S

[itex]\Delta[/itex]H = H[itex]^{L}[/itex] - H[itex]^{S}[/itex]

[itex]\Delta[/itex]S = S[itex]^{L}[/itex] - S[itex]^{S}[/itex]

At eqilibrium melting temperature T[itex]_{m}[/itex] the free energies of the liquid and solid are the same.

So [itex]\Delta[/itex]G = 0

[itex]\Delta[/itex]S = L/T[itex]_{m}[/itex]

If the liquids is supercooled by even a small amount then it become energically favourable for the liquid to become a solid and realese latent heat.
 


Page 187 goes into more detail.

When a particle of solid nucleates it's free energy will depend on its size

[itex]\Delta[/itex]G = -[itex]\frac{4}{3}[/itex][itex]\pi[/itex]r[itex]^{3}[/itex][itex]\Delta[/itex]G[itex]_{v}[/itex] + 4[itex]\pi[/itex]r[itex]^{2}[/itex][itex]\gamma[/itex][itex]_{sl}[/itex]

Subscript r and v represent radius and volume terms and [itex]\gamma[/itex] is surface energy of the interface.

There is a critical radius r[itex]^{*}[/itex]. If r < r[itex]^{*}[/itex] then the system can lower it free energy dissolution of the solid. If r > r[itex]^{*}[/itex] then the system can lower its free energy by growing the solid.

[itex]\Delta[/itex]G[itex]_{v}[/itex] = L[itex]_{v}[/itex]ΔT/T[itex]_{m}[/itex]
[itex]\Delta[/itex]T is the undercooling temperature.

r[itex]^{*}[/itex] = (2[itex]\gamma^{3}_{SL}[/itex]T[itex]^{2}_{m}/L_{v})(\frac{1}{ΔT^{2}}[/itex])

So if you could measure this critical radius you could determine the melting point for the undercooling required.
 
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If you agree that the formation of a chemical bond tends to lower free energy (leaving aside the details of enthalpy and entropy), then a state which maximizes the bond density will tend to be the most stable. Solids are more close packed than liquids (i.e., they have a higher bond density), thus they tend to represent a lower energy state.

Solids melt when the thermal energy of its constituent atoms/molecules overcome the bond energy. (This is why, near the melting point of most materials, the product of the coefficient of thermal expansion and absolute temperature gives a strain on the order of ten percent - much more and the solid is no longer stable -- the bond length becomes too great!)

Once you understand this, a more interesting question is why does the solid assume the crystal symmetry that it does? (i.e., why aren't all solids close packed) But I suspect this is a little beyond what you're looking for.
 


I agree that free energy decreases when a chemical bond is formed. Is it due to release of heat of fusion and decrease in entropy? In what form was the excess energy (heat of fusion) stored in liquid state?

The question which uby has mentioned was troubling me from some time. I have read that all metals are not FCC/HCP because it depends on electronic structure of atoms. But I am not fully satisfied.
 


pukb: Entire theories of bonding have been created whose primary purpose are to explain the observed structures and properties of materials. Solid state physics, physical and molecular chemistry, etc. Unfortunately, there isn't a very concise explanation and you will need to endure a lot of reading to fully grasp these theories. I myself am not fully versed in anything but the most introductory aspects of most of these theories.

A couple quick points: generally, the entropic contribution to the total free energy of condensed phases is small compared to the enthalpic contribution - this is not to be confused with the contribution to the free energy of solution/mixing/etc., where there can often be zero enthalpic contribution.

Most liquids exhibit short-range order (on the molecular length scale) but lack long-range order (in the order of molecules) unlike solids. This lack of long-range order is manifested in a lower bond density. The greater the bond density, the lower the overall free energy. For example, [SiO4] tetrahedra in a silicate liquid are mostly corner-shared with each other (allowing for many degrees of freedom and an increased free volume) while in the solid they can exhibit much more rigid bonds along faces and/or edges depending on the crystal structure.
 
  • #10


Astronuc said:
METALS tend to form along crystalline planes.

To make amorphous materials, particularly in metals, usually requires rapid solidification.

Fixed that for you. Be aware, however, that this is misleading. Crystallinity is merely a subset of a few types of solids; or more rigorously defined as a description of a microstructure with long-range order (theoretically infinite LRO). For instance, there exist crystalline metals, polymers, ceramics, et al.

As far as solidification is concern, it's an energetically driven phenomenon that, in the most refined way known, is detailed above by bm0p700f from the exact textbook that I, too, favor.

I agree that free energy decreases when a chemical bond is formed. Is it due to release of heat of fusion and decrease in entropy? In what form was the excess energy (heat of fusion) stored in liquid state?

Heat of fusion, or more generally just latent heat, is (assuming you know the definition already here) actually "hidden." It's not used in the chemical bonding, but is rather a form of potential energy associated with separating atoms.
 

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