Handout 3: Casting of metals Flashcards

1
Q

Give the process and steps of sand casting

A
  1. A solid re-usable pattern (often wooden) is made of the component.
  2. Sand with a small amount of resin binder is packed around the pattern in a box called a drag.
  3. The drag is inverted and the pattern is lifted out, leaving a cavity. In-gates and runners may be carved or moulded into the sand.
  4. Interior detail may be produced by inserting a core (also molded out of sand) into the cavity. The upper part of the mould( the cope ) is formed from sand, incorporating a pouring basin, a sprue, vents, runners and risers(either moulded from patterns - e.g. runner pin and riser pin shown.
  5. Mould bolted together, metal poured in. Once the casting has solidified, the sand mould and any cores are broken up and brushed out.
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2
Q

What are the different classifications of casting processes?

A

Ingot or Continous casting:

  • Permanent mould

Shaped casting

  • Permanent mould
  • Permanent pattern
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3
Q

Describe ingot or continous casting

A
  • Continous casting for most high-volume steel; “direct chill” (DC) casting for wrought aluminium alloys.
  • Ingot casting (permanent mould) used for lower volume alloys.
  • Post-processing:
    • Homogenisation + Thermomechanical processing, e.g. hot/cold rolling, forging, extrusion + heat treatment
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4
Q

Describe shaped casting

A

Permanent mould

  • Simple shapes: need easy removal of mould, and multiple use.
  • Moulds expensive(tool steel; may make 103-106 castings).
  • Typically used for large numbers of small parts
  • Examples:
    • pressure die casting
    • gravity die casting
    • centrifugal casting

Permanent pattern

  • More intricate shapes: mould is created around a pattern and destroyed to remove the casting.
  • Low setup costs and production rates.
  • Used for larger parts, or when small production runs.
  • Examples:
    • Sand casting
    • Investment casting
    • Evaporative mould casting

Post processing:

  • “Fettling” (trim solidified feeder channels)
  • Machine/grind critical areas (improve tolerances and surface finish around joints, seals, contact surfaces)
  • Drilling
  • Some casting heat-treated to improve properties.
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5
Q

Give the advantages of the different permanent pattern moulding methods.

A

Sand casting

  • Advantages: Versatile, low material and equipment costs, OK for large simple parts, internal details and re-entrant features possible.
  • Disadvantages: Poor dimensional accuracy and surface finish, not suitable for thin sections; relatively high labour costs; “dirty” process.

Investment casting

  • A hybrid process: here “permanent pattern” actually means a permanent mould is used to make an expandable pattern. This pattern is covered in an expandable ceramic/ refractory shell, in which the casting itself is produced.
  • Advantages: Excellent accuracy and surface finish
  • Disadvantages: Limited to small parts; labour intensive; more expensive

Evaporative mould casting

  • Closely related variant, using a polystyrene foam pattern.
  • Advantages: High accuracy and surface finish (especially with small-bead polystyrene); lighter patters than wax, so suitable for large parts.
  • Disadvantages: Labour again relatively high
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6
Q

Give descriptions of the different types of permanent mould casting.

A

Pressure die casting

  • Externally applied pressure permits use of higher viscosity fluid, thinner sections, and minmises waste from runners, risers etc. Susceptible to entrapped bubbles due to turbulance, which can be detrimental to properties.
  • Limited to low-melting point alloys (because the dies must not distort or wear whilst making many thousands of castings)

Gravity die casting

  • Variant process using gravity feed (as in sand casting) but with permanent mould in two separable parts, as in pressure die casting.

Centrifugal casting

  • Used for axisymmetric hollow parts (e.g. pipes)
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7
Q

What are the differences in alloy compositions between casting alloys and wrought alloys.

A

Casting uses dedicated alloy compositions that provide castability(i.e the ability to fill moulds, without major defects). This is controlled by the melt viscosity, the freezing range between liquidus/solidus and the desirability of a lower melting point.

Compositions for thermomechanical (wrought) processes are dominated by solid-state formability and microstructural control for properties (e.g. by heat treatment). For example:

  • wrought carbon steels (Fe + 0.1-0.8wt% C): hot/cold formed.
  • cast iron (Fe + 4wt% C): only cast
  • wrought Al alloys (Al + 1-5wt% Mg, Cu, Zn or Si): hot/cold rolled, extruded
  • cast Al alloys (Al + 12% Si): only cast

Castings generally have poorer mechanical properties than wrought counter parts, largely because of porosity, and high content of second phases (brittle). But casting plus heat treatment can lead to high-quality componentes (e.g. jet engine nickel alloy turbine blades)

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8
Q

What is Chvorinov’s rule?

A

Solidification time of a section is proportional to [Volume/Surface area]2

ts = k(V/A)2

Physical basis:

  • k(V/A) = shortest length scale
  • ts = k(heat flow distance)2
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9
Q

What are the three main physical origins of defects?

A

fluidity

turbulance

shrinkage

(Porosity is also caused by dissolved gas being released during solidification)

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10
Q

What are Misruns and cold shuts, what is the solution?

A

Misrun: caused by lack of fluidity

Cold shut: caused by streams of metal bring too cold to fuse.

Solutions:

Redesign running and gating system (position, size and number of ingates and vents). Increase fluidity by raising pouring temperature or preheating mould, or by changing alloy composition (lower freezing range).

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11
Q

What turbulance defects in moulds ?

A

Turbulance may arise close to where metal is poured into mould, or within the mould if there are abrupt changes in section.

  • air may be trapped, leading to the formation of large-scale porosity. The surface of the liquid metal is often oxide covered: with turbulent flow, more oxide is formed and entrapped in the casting.
  • Pressure die-casting always results in turbulance and porosity.
  • In sand casting, the mould may also be damaged by rapid metal flow at ingates, leading to sand particle defects in the casting, and causing loss of dimensional accuracy of the casting.
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12
Q

Describe what shrinkage defects are in moulds.

A

Metals shrink considerably during casting, both due to thermal contraction (in liquid and solid state), and due to crystallisation on solidification.

Moulds are designed to hold a reserve of molten metal (the “risers”) to allow metal to be fed in during solidification. Hence the metal in the feeder head must solidify last, otherwise parts of the casting may be starved, leading to porosity.

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13
Q

What are “mushy freezers” and what are their associated problems?

A

Feeding the mould to accommodate shrinkage is more difficult in “mushy freezers” i.e. alloys with a large freezing range (between liquidus and solidus). Liquid percolates more slowly through the semi-solid region, giving a greater risk of shrinkage defects. This is one advantage of using eutectic compositions.

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14
Q

How are issues such as stress buildups (leading to hot tearing) or shrinkage cavaties avoided?

A
  • Maintaining a more uniform mould section
  • Making changes in section more gradual rather than sharp corners.
  • When section changes are unavoidable, the solidification patern may be altered by the use of chills, to cause early solidification (and thus strengthening) in vulnerable regions (e.g. embeddding metal inserts in the sand mould.)
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15
Q

What is Gibbs free energy? and explain how it becomes the driving for solidification. (Draw a G vs T graph)

A
  • G = H - TS (H enthalpy, absolute temperature T, entropy S)
  • On cooling a liquid below melting temperature, the system can reduce its free energy by transforming from liquid to solid. The free energy difference G between the two states is the driving force (approximately proportional to the undercooling change in T)
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16
Q

Explain homogeneous nucleation.

A

Solid crystals first nucleate: i.e. form spontaneously within the liquid when cooled below its melting temperature. Nuclei have a critical radius above which they are stavle and subsequently grow - the greater the driving force, the smaller the critical radius.

Homogenous nucleation - involves the formation of isolated solid spheres within the melt.

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17
Q

Explain heterogeneous nucleation

A

Involves the formation of a spherical cap of solid on a substrate in contact with the melt (i.e the mould wall or a solid particle within the liquid)

The undercoolig for hetergeneous nucleation is typically a few degrees - much smaller than for homogeneous - so nucleation from surfaces and particles dominates in casting.

Heterogeneous nucleation is characterized by the contact angle, which depends on the balance between three surface energies: γSLNLNS.

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18
Q

Draw and explain the initial transient of 1D solidification of liquid with initial concentration Co.

A
  • Solidification starts at temperature T0.
  • For typical solidification rates, there is essentially no diffusion in the solid, hence the depleted concentration gradient in the solid is “locked in”, with the excess solute being pushed into the liquid ahead of the solid-liquid interface: this is segregation. Solute diffusion in the liquid extends some distance ahead of the interface, but the concentration profile as maintained as the interface also moves to the right.
  • With each incremental advance of the interface, the solute level in the solid stays below average for the alloy. Hence the peak solute concentratio i the liquid at the interface rises, with that in the corresponding solid maintaining the partition coefficient ratio, such that Cs= kCL.
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19
Q

Draw and explain the steady state of 1D solidification of liquid with initial concentration Co.

A

As the interface advances, Cs rises asymptotically towards Co, at which point steady state is reached.

The solidification temperature = T1, with Cs=Co and Cl=Co/k.

The “bow-wave” of elevated solute advances at the same speed as the interface.

20
Q

What is macrosegregation?

A

In a real casting, solidification proceeds from opposing walls of the mould towards the centre. Hence the excess solute from both sides concentrates into the last part to solidify. This is called macrosegregation.

This leads to poor mechanical properties (e.g. high concentrations of weak second phases in the central grain boundaries). And if the segregating solute is a gas, this may lead to the formation of macroporosity in the centre of the casting.

21
Q

What is constitutional supercooling of alloys?

A

Consider again the steady-state distribution of composition. From the phase diagram, the higher the concentration of the liquid, the lower its solidification temperature. This temperature therefore has essentially the same form of the concentration curve, but inverted.

Now superimpose the actual temperature gradient in the casting (decreasing from right to left, the direction of head conduction). This temperature is equal to the local solidification temperature at the interface, but there are then two scenarious, depending on the gradient in the temperature (dT/dx) compared to the gradient in the local solidification temperature (dTm/dx).

  • case (i): (dT/dx) > or = (dTm/dx): T in liquid everywhere above its local melting point; solidification is stable at the interface (leading to a planar solidification front or “cellular growth of a few grains”.
  • case (ii): (dT/dx) < (dTm/dx): in a region ahead of the interface, T in the liquid is below its (local) melting point: this is known as constitutional supercooling, since it is a gradient in composition (coupled with a thermal gradient) that leads to the supercooling. Here solidification is unstable, leading to dendrite formation.
22
Q

What are dendrites?

A

In constitutional supercooling, there is a greater driving force for solidification ahead of the solid-liquid interface than at the interface itself. Unstable growth occurs as follows: if a small part of the solid interface spontaenously extends into the surrounding liquid, it can continue growing rapidly into the melt, leading to long thin crystals. The same behaviour may then be repeated on the sides of these crystals, giving secondary side arms.

  • The distinctive crystal shape formed during solidification is known as a dendrite.
  • Once the arms of a given dendrite meet, they form a single grain, and their characteristic structure is not visible - the final structure only reveals the grain boundaries where the crystal orientation changes.
23
Q

Why is it often desirable to ensure that equiaxed grains form the major part of the casting?

A
  • Finer grain size: improves strength
  • Reduce the extent of macrosegregation
  • Interfaces between columnar grains contain high proportions of impuritiies/gas, due to lateral segragation. Fully columnar casting can contain interconnected porosity, particularly in mushy feeders where feeding liquid metal into these regions is difficult. This may lead, for example, to leaking in cast pipes.
24
Q

What different ways can nuclei for grains in the equiaxed zone arise?

A
  • Oxide particles (or other impurities) entrapped during pouring.
  • Inoculants (grain refiners): small amounts of specific solid (fine powder) added just before puring. Inoculants must have a very low contact angle to promote easy nucleation (the inoculant particles become coated in solid, overcoming the critical radius barrier). e.g. addition of 0.05-0.1% TiB2 is standard for cast Al alloys.
    • Turbulence in melt may break of dendrites, which form stable nuclei in the melt.
25
Q

Explain how columnar zone growth in cast alloys leads to macro-segregation.

A

A columnar zone through the whole casting leads to inhomogeneity on the scale of the casting. Impurity accumulations in the centre of the casting lead to a plane of weakness. In square section (e.g. in continous casting), the columnar grains impinge along the diagonals, again giving planes of weakness.

26
Q

What are techniques to remove impurities before casting?

A

It is expensive or impossible to remove the impurities before casting. One solution is additional alloying, to trap the impurities in a harmless form throughout the casting.

Example: all C steels cotain sulphur as an impurity; the addition of Mn leads to the formation of a dispersion of MnS particles throughout the casting, rather than letting the S segregate to the grain boundaries, forming brittle FeS.

A second solution is to promote the formation of the equiaxed zone, trapping impurities in more dilute concentrations over a large area of grain boundary: grain-scale segragation.

27
Q

What is dendrite-scale segregation?

A
  • Segregation also occurs between the dendrites arms (primary and secondary)
  • The dendrite arm spacing refers to the length scale of the secondary dendrite arms (typically a few micro m). It is often cited as a key length-scale of a cast microstructure (i.e. the scale of inhomogeneity that can be influenced by heat treatment).
  • Grain-scale/dendrite-scale is preferable to macro-segregation, but high solute/impurity contents at grain boundaries can still cause problems: localized corrosion, or coarse precipitation reducing toughness or ductility.
28
Q

Explain homogenisation heat treatment.

A

Homogenisation is a prolonged “soak” of a casting at high temperature in the single phase field (e.g. 24 hours at 530-580*C for Al alloys, with melting point c.630*C), This requires bulk diffusion of the components that are distributed inhomogenously. In most cases the alloying additions form substitutional solid solutions (rather than interstitial), and therefore are inherently slow to diffuse - hence high temperatures and long hold times are needed.

29
Q

How is the degree of homogenisation estimated?

A

Estimated using the rule-of-thumb diffusion equation:

x2 = Dt

where diffusion of an element takes place over a characteristic distance x in time t, with a diffusion rate D = D0exp(-Q/RT).

30
Q

Explain what porosity is and solutions to this problem in casting.

A

Porosity is common in castings due to dissolved gas coming out of solution during solidification. Gases may be absorbed from the atmosphere, or may be injected as part of prior processing - e.g. oxygen is injected in steel-making to burn off the excess carbon in pig iron (to the much lower level needed in the steel), leaving residual oxygen, CO and CO2 dissolved in the steel.

Vacuum degassing, though expensive, improves casting quality - the metal is held under vacuum before casting. But as with other impurities, dissolved gas can also be rendered harmless by converting it into solid particles (e.g. oxides) during solidification.

Example: ‘killing; a steel means adding Al powder to produce Al2O3 particles, removing much of the oxygen from solution.

31
Q

Give a brief description of continous casting and how it avoids porosity.

A

Over 90% of steel is produced by continous casting. the steel is vacuum degassed before casting, but macroporosity problems are avoided: most released gas escapes upwards through the liquid “sump” into which liquid steel is fed continously.

32
Q

Draw the diagram for the as-cast and homogenised version of Al-4% Cu. Explain the differences.

A
  • As-cast:
    • Dark regions are inter-dendritic regions and grain boundaries.
    • The contrast arises from etching of impurities, and from porosity.
  • Homogenised:
    • Dendritic structure within grains no longer visible: impurities have redistributed.
    • Dark spots in the grain are porosity trapped between dendrite arms.
  • Note that microporosity remains after homogenisation: the pores are filled with gas mostly in the form of molecules rather than atoms, and the diffusion rate for molecules is very small (due to their size).
33
Q

How is microporosity removed from castings?

A

Microporosity in ingots is largely removed by hot rolling - but this is not a solution for near-net shape castings. Hot isostatic pressing(HIPing) can be used to remove microporosity - costly, but provides marked improvement in mechanican properties. Easiest for Al and Mg alloys, where HIPing temperature required is comparatively low (so relatively economical).

34
Q

What are the advantages of using eutectic composition alloys in casting?

A
  • Low melting temperature -> Cheap heating cost + faster production rates
  • Low solidification (“freezing”) range means high fluidity and easiest to feed: lower shrinkage defects, lower porosity.
35
Q

What are the consequences of using eutectic alloy compositions in castings?

A

Eutectics are two-phase material with a high volume fraction of a fine-scale hard second phase - which suggests potential for precipitation hardening. However, these second phases often non-metallic and brittle (e.g. Si in Al casting alloys). This has implications for strength and toughness - these properties depend on the morphology (i.e size and shape) of the second phases fomed in the casting. This is sensitive to whether the second phase is metallic or non-metallic.

36
Q

Explain how metal and non-metal phases solidify and their effects on the alloys properties.

A
  • Metals solidify easily from a liquid, because the surface energy of the solid-liquid interface is relatively low, so the surface can be atomically “rough” and there are many sites available for atoms to attach themselves to the new solid. This leads to rounded, ‘blobby’ solid particles.
  • Non-metals (e.g. graphite, silicon) have a higher surface energy with the liquid, so prefer to form an atomically smooth surface. Growth is easiest parallel to the interface. Overall this is slower than forming a solid metal phase, and leads to elongated, angular particle shapes, such as needles of flakes.
37
Q

Explain poisoning.

A

particle morphology such as needles is not good news for toughness - the brittle phases behave like cracks. The solution is to modify the growth by poisoning: atoms of an alloy addition which half the growth of steps, leading to smaller more rounded particles of the brittle second phase.

38
Q

Explain the weaknesses of Al-13% Si eutectic are avoided.

A

Al-13% Si eutectic

  • In unmodified Al-Si, the silicon forms a fine dispersion of hard, brittle needles in the soft Al matrix. Considerably improved strength, toughness and ductility are achieved by poisoning : adding just 0.01% sodium immediately before casting modifies the growth to give finer, more rounded particles of silicon.
39
Q

Describe the microstructre of grey cast iron, and the weaknesses that arise from the flakes.

A

Microstructure: ferrite + graphite (+ iron carbide, sometimes as pearlite, depending on the composition and heat treatment)

The graphite morphology is an interconnected network of flakes:

The graphite flakes are weak, and act like cracks - so unmodified cast iron has poor tensile properties. The flake size scales inversely with the velocity of the solid-liquid interface: faster cooling gives more nucleation, smaller flakes and high strength. Hence smaller cast iron castings tend to have higher strength.

The graphite flakes are good for damping mechanical vibration (so useful for machine tool mountings), and cast iron can be machined easily without lubricant (as the graphite provides sufficient lubrication).

40
Q

What are the compositions required to produce ‘nodular’ cast iron.

A

Improved mechanical properties can again be achieved by poisoning: changing the growth mechanism of the (non-metallic) graphite. In this case, the addition of approx. 0.5wt% of magnesium or cerium causes the graphite to form as rounded nodules, significantly improving the strength and toughness.

41
Q

What are the dimensional advantages on solidification of cast iron.

A

A further benefit of grey cast irons is that they show very low shrinkage. Graphite is a low density phase, so the formation of graphite counteracts the contraction of the iron on solidification. For near-eutectic compositions of grey cast iron there is effectively zero volume change on solidification - useful for producing casting directly to final size and shape.

42
Q

Give the properties of the three base alloys (and what they need improvement on):

Aluminium

Iron

Nickel

A

Aluminium, Al: low density, stiff relative to weight, but needs strengthening

Iron, Fe: inherently strong, tough and abundant, and can be greatly strengthened.

Nickel, Ni: high melting point, enhance for optimum creep resistance.

43
Q

List the different alloy additions for properties

A
  • primarily directly, by producing two-phase microstructures and precipitation hardening (and/or solid solution hardening), e.g.
    • C in steels: Fe3C (pearlite)
    • Si in Al: Al-Si solid solution + eutectic Si
    • (W in alloy steels: more stable carbide, WC, and effective solid solution, both for high temperature strength)
  • Some additions work indirectly, by changing the response to the environment or to temperature, or by influencing grain structure, or by modifying the morphology of brittle phases, e.g.
    • Cr: corrosion resistance in stainless steels
    • Ni: keeps stainless steel FCC, avoiding ductile-brittle transition(so steels remain tough at cryogenic temperatures)
    • Incoulants in castings: TiB2 in Al castings to nucleate fine grains
    • Poisoning in castings: Na in Al-Si castings to poison growth of large Si flakes, Mg or Ce in grey cast iron to poison growth of graphite flakes.
44
Q

List the different alloy additions for processing.

A
  • Additions to make it easier to process an alloy, e.g. Si in Al casting alloys: lower melting point, greater fluidity.
  • Ni,Cr,Mo,W in C steels: increase hardenability - enabling Q/T properties in thicker sections and reducing risk of quench cracking.
45
Q

List different impurity “fixers” for alloying.

A
  • Mn in C steels to form harmless MnS particles, rather than segragating S to grain boundaries (where it forms brittle FeS)
  • Al in steels: add to melt before casting (“killing” the steel) to form harmless solid Al2O3 particles, rather than the dissolved oxygen forming porosity.