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Working with Phase Diagrams
Overall composition of the alloy Liquidus and solidus temperatures Limits of solid solubility Chemical composition of phases at any temperature Amount of phases at any temperature Structural change with temperature
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Isomorphous Phase Diagrams
Phase diagrams of components that are completely soluble to each other (Type 1 phase diagrams). Example: Copper – Nickel phase diagram. Wt% Ni Both Cu and Ni can go into solution completely into each other in the solid state without forming any supersaturated solution i.e., there is no solubility limits.
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Phase Diagram Nomenclatures
Liquidus Start of solidification or, end of liquification Temperature X Y % Y added Liquid Solidus End of solidification or, start of liquification Liquid + Solid Freezing range Not to be confused with Solvus, which indicates the limit of solid solubility in a solid solution Solid Composition of alloy Relative amounts of X and Y The scale can be in weight %, atomic % or mole % Phase diagram with complete solubility of one component into another (Type 1 Phase Diagram)
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Chemical composition of Phases
Chemical composition of each phase in the system (indicating how much X and Y in the phase). For systems having more than one phase, each phase will have a unique chemical composition which will be different from each other, and will also be different from the overall composition. Not to be confused with overall composition of the alloy. Relative amounts of Phases For system having more than one phase, relative amount is the amount of each phase relative to overall amount of the alloy (indicating kg of each phase in overall weight of the alloy). Depends on temperature and composition of the alloy. Not to be confused with composition of phases.
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The Cooling Curve Cooling curve indicates the gradual change in temperature with time during cooling of alloy X Y % Y L S L+ S TX Temperature ARREST POINTS Temperature Time Freezing range Alloy 1 Solid Liquid Liquid + Solid start of solidification end of solidification TX Pure metal X Alloy 1
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Interpreting Phase Diagrams
Predicting the nature of stable phases as a function of T, P and X Number and types of phases Composition of each phase Relative amount of each phase
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Predicting the nature of stable phases as a function of T, P and X
Independent variables: T and X ( always P=1 atm) one-phase area (L) two-phase area (L + a) one-phase area (a)
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Number and types of phases
Phase diagram rule #1: If we know the alloy composition, C0, then we can tell the number and type of phases present in the structure at any given temperature. wt.%Ni Point A: (30%Ni, 1225°C) Phases are: L and a Point B: (60%Ni, 1100°C) Phases are: a only Cu-Ni Phase Diagram
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Composition of each phase
Phase diagram rule #2: Tie Line Rule If we know C0, then we can tell the composition of each phase at any temperature. tie line At TA: L phase only CL = 35%Ni At TB: L and a phases CL = Ca = Cliquidus = 32%Ni Csolidus = 43%Ni At TD: a phase only Ca = 35%Ni
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Relative amount of each phase
Phase diagram rule #3: Lever Rule If we know C0, then we can tell the weight fraction of each phase at any temperature. Consider C0 = 35 wt.%Ni At TA, only L phase WL = 100 wt.% At TD, only a phase Wa = 100 wt.% At TB, both L and a phases WL = = = 73 wt.% 100 (43-35) 43-32 100 S R+S Wa = = = 27 wt.% 100 (35-32) 43-32 100 R R+S
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To summarise: Finding the composition in a two phase region:
1. Locate composition and temperature in diagram. 2. In the two phase region, draw a tie line at the given temperature. 3. The liquid composition will be on the liquidus line and the solid composition will be on the solidus line. Note the intersections with phase boundaries. Read compositions at the intersections. Finding the amounts of phases in a two phase region: 1. Locate composition and temperature in diagram. 2. In the two phase region, draw a tie line at the given temperature. 3. Fraction of a phase is determined by taking the length of the tie line to the phase boundary for the other phase, and dividing it by the total length of tie line.
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Problem One kilogram of an alloy of 70% Pb and 30% Sn is slowly cooled from 300ºC. Calculate the following: 1. Chemical composition of the liquid and a phase at 225ºC. 2. Weight % of liquid and a at 225ºC.
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Problem One kilogram of an alloy of 70% Pb and 30% Sn is slowly cooled from 300ºC. Calculate the following: R S 1. Chemical composition of the liquid and a phase at 225ºC. 2. Weight % of liquid and a at 225ºC. CL = 45 wt.% Sn Ca = 17 wt.% Sn 100 (30 – 17) WL = = 56 wt.% 100R R+S = 100 (45 – 30) Wa = = 54 wt.% 100S
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Development of Microstructures
The microstructural development depends on the overall composition and the cooling rate of the alloy 1300 1200 1100 20 30 40 50 C0=35 T (°C) wt.% Ni L+a L a Equilibrium Cooling of Alloy A C0=35 B 34 46 C 43 32 Point A L: 35 wt.%Ni Point E a: 35 wt.%Ni D 36 24 Point D a: 36 wt.%Ni L: 24 wt.%Ni E Point C a: 43 wt.%Ni L: 32 wt.%Ni Point B a: 46 wt.%Ni L: 34 wt.%Ni Binary isomorphous phase diagram of Copper and Nickel
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All microstructures at a glance
Summary of Solidification Process Solidification begins at the liquidus line and continues upon cooling The composition and amount of the solid and the liquid change gradually during cooling Solid phase grows by consuming all the liquid and solidification ends at the solidus line
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Non-Equilibrium Cooling of Alloy
The cooling of alloy is so fast that the time required for transformation is not given. Faster cooling rate cored structure – a.k.a. microsegregation Slower cooling rate equilibrium structure Uniform Ca 35 wt.% Ni First a to solidify: 46 wt.% Ni Last a to solidify: <35 wt.% Ni Ca composition is equals to C0 throughout Ca changes during solidification
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Problem with cored structure
On re-heating, grain boundaries will melt first, as they are rich in lower melting-point constituent. This can lead to premature mechanical failure! Lighter phase with low Al content Darker phase with high Al content Cored structure in Al-Cu alloy Homogenising the cored structure Microsegregation or the cored structure can be eliminated by reheating the material at a higher temperature. Diffusion of inhomogeneous element takes place. Macrosegregation, however, cannot be eliminated by reheating.
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