Imaging of Microstructural Features and Local Stiffness of α and β Phases in Titanium Ti-6Al-4V Alloy by Atomic Force Acoustic Microscopy

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5th International Workshop NDT in Progress Meeting of NDT experts, October 12 14, 2009 Prague, Czech Republic, Hotel and Congress center Floret Imaging of Microstructural Features and Local Stiffness of α and β Phases in Titanium Ti-6Al-4V Alloy by Atomic Force Acoustic Microscopy Jonas Rabe, Ute Rabe, Sigrun Hirsekorn Fraunhofer Institut für zerstörungsfreie Prüfverfahren (IZFP) Campus E3.1, 66123 Saarbrücken

Outline Principle of Atomic Force Acoustic Microscopy (AFAM), dynamic operation mode of an Atomic Force Microscope (AFM) in the ultrasonic frequency range Mechanical models of AFM cantilevers and the contact between a sensor tip and a sample surface, resonance vibrations of the cantilever without and with sample contact Application of AFAM to image microstructural features and local stiffnesses of α and β phases in the Titanium alloy Ti-6Al-4V

Frequencies and Wavelengths of Elastic Waves Hypersound

Sensors of Commercial Atomic Force Microscopes Small elastic beams: Length: a few 100 µm, width: a few 10 µm, thickness: a few µm, Sensor tip: Radius of a few nm up to of a few 100 nm, Material: Silicon single crystal (cantilever and chip ond piece), Vibration resonances in the ultrasonic frequency range, i.e. usable as a near field ultrasonic probe. Optical microscopy image SEM image Cantilever 10 µm Sensor tip Typical values: 1. Free bending resonance frequency: 10-300 khz Spring constant: ca. 0.1-60 N/m

Dynamic AFM Operation Modes with Ultrasonic Frequencies - Atomic Force Acoustic Microsopy (AFAM), vertical und lateral, - Ultrasonic piezo-mode, - Ultrasonic Friction Force Microscopy (UFFM) exploit flexural and torsional vibration resonances of AFM cantilevers Imaging of sample surfaces: Spectroscopy: - Amplitude Contact resonance spectroscopy - Phase (Quantitative determination of - Contact resonance frequency local material parameters)

Atomic Force Acoustic Microscopy (AFAM), Set-Up U. Rabe and W. Arnold, Appl. Phys. Lett. 64 (1994) 1493 O. Kolosov and K. Yamanaka, Jap. J. Appl. Phys. 32 (1993) 22 K. Yamanaka and S. Nakano, Jap. J. Appl. Phys. 35 (1996) 3787 K.B. Crozier et al. Appl. Phys. Lett. 76 (2000) 1950.. AFM: Atomic Force Microscopy

Flexural Vibrations of a Beam of Constant Cross Section Equation of motion of flexural vibrations in a bar: E: Young's modulus ρ: Mass density γ: Damping constant A: Cross section area I: Area moment of inertia Boundary conditions: clamped-free beam solutions from textbooks clampled-surface coupled beam nonlinear force curve

Quasi-Static Force Curve Between a Sensor Tip and a Sample Calculated from a measured AFM force distance curve, Silicon cantilever in contact with a chromium sample Setpoint z Force [10-8 N] e Repulsive forces 1 k* = -0.2-0.1 0.1 z [nm] -df/dz(z -1 e ) -2-3 -4 Attractive forces -5 Repulsive region: Hertzian model of the contact forces Relation between the contact stiffness k* and the local indentation modulus of the sample surface Equivalent for shear forces and torsional resonances shear modulus S. Hirsekorn Nanotechnology 8, 1997, 57-66.

Cantilever Beam and Contact Model k*, k* lat : Vertical and lateral contact stiffness γ, γ lat : Vertical and lateral interaction damping L+L': Length of the cantilever L: Position of the sensor tip h: Length of the sensor tip α 0 : Angle between cantilever and sample surface k C : Static spring constant of the AFM cantilever beam U. Rabe Applied Scanning Probe Methods II, Springer, 2006, 37-90.

Hertzian Model of the Mechanical Contact AFM tip Sample Contact radius Contact stiffness P = 2aE* Isotropic materials 1 2 (1 νs) (1 = + ν E* E E S E T : Young s modulus tip ν T : Poisson ratio tip E S : Young s modulus sample ν S : Poisson ratio sample T 2 T ) Lateral contact stiffness k lat* = 8aG * E*, G*: Effective Young's and shear modulus of the contact D. Maugis Contact, Adhesion and Rupture of Solids, Springer, 2000.

AFAM Contact Resonance Spectra, Nonlinear Forces Sample: silicon; cantilever: silicon, 2nd contact bending mode Increase of the excitation amplitude: softening effect, asymmetric shape of the resonance peak, and amplitude jump Inversion of the direction of the frequency scan: hysteresis

Topography, AFAM, and Piezo-Mode Images Polycritalline Barium Titanate Ceramic, imaging of ferroelectric domains Topography, Height scale 20 nm AFAM, 860 khz, Amplitude Image Piezo-Mode, 865 khz, Amplitude Image Diamond coated cantilever; Spring constant: 54 N/m; 1st bending mode; Static load: 540 nn; Image size: 10 µm x 10 µm U. Rabe, et al. Journal of Physics D Applied Physics, Vol. 35, 2002, 2621-2635.

AFAM Amplitude Images of the First Bending Mode Contact stiffness k* Small Frequency Large Area with higher contact stiffness Amplitude of Cantilever vibration 0 V 8 V Sample: PIC 151, Polycritalline Barium Titanate Ceramic (PTC) Imaging of ferroelectric domains within a grain, the different orientations influence the elastic behaviour. 1. Bending contact resonance: 697.5 khz Image size: 4.5 x 4.5 µm 2 U. Rabe, et al. Journal of Physics D Applied Physics, Vol. 35, 2002, 2621-2635.

Topography and AFAM Image of Nanocrystalline Nickel Cantilever spring constant: kc = 48 N/m, Free bending resonances: f1 = 166 khz f2 = 1031 khz Sample: Nanocrystalline nickel Grain size: 167 nm Topography image, Height scale 10 nm Image size: 1.5 x 1.5 µm2 Contact resonance frequency AFAM image, frequency scale: 730 750 khz U. Rabe, et al. Surface and Interface Analysis Vol. 33, 2002, 65-70.

AFAM Contact stiffness Image of Nanocrystalline Nickel Contact stiffness k * [N/m] 2 1 f free modes f contact modes Flexural Beam Theory k* Contact Stiffness k* Hertzian Theory Indentation Modulus M Indentation modulus M of nickel: 3 Image size: 1.4 x 1.5 µm 2 Experiment [GPa]: M Pos 1 = 234 M Pos 2 = 184 M Pos 3 = 176 Calculated from single crystal literature values [GPa]: M (111) = 223 M (110) = 218 M (100) = 202 U. Rabe, et al. Surface and Interface Analysis Vol. 33, 2002, 65-70.

Titanium - Titanium: transition metal, strong, highly creep resistant, light, heatresisting, biocompatible, and corrosion resistant broad field of industrial applications. - Primarily two different crystal structures in titanium: the hexagonal close-packed (hcp) α-phase and the body-centred cubic (bcc) β-phase. - Pure titanium: 100% α-phase at room temperature if cooled down slowly enough to allow diffusion; above the β transition temperature (BTT = 882 C for pure titanium) the bcc structure is stable. - Transition of theβ-phase during cooling: Depending on temperature and cooling rate theβ-phase transforms either into the metastable β-phase, the stiff hcp α -, or the soft tetragonal closepacked (tcp) α -martensite structures. - Strong variations of the bulk properties with the ratio of the phases: the hcp α-phase with strong elastic anisotropy has the highest indentation modulus (~117 GPa); the metastable bcc β-phase with significantly lower anisotropy has the lowest indentation modulus (~82 GPa). - Forming preferred just above the β transition temperature: the bcc-structure contains more slip planes, i.e. is easier to deform than the hcp-structure.

Titanium Alloy Ti-6Al-4V Titanium alloys: Stability of α- und β-phase below the β transition temperature by adding appropriate elements to the fluid titanium; stabilisation of theα-phase and increase of β transition temperature by e.g. N, O, C, Al, Sn and Zr; stabilisation of theβ-phase and decrease of β transition temperature by e.g. Fe, Bi, Mn, Cr, Co Mo, Ni, Pb, Cu, V und Nb (in order of decreasing effect). Most common titanium alloy: Ti-6Al-4V - 60% of the titanium market, 80% thereof aircraft industry; - Al for α-, V for β-phase stabilisation, β transition temperature ca. 1000 C; - Slow cooling to room temperature (i.e. time for diffusion processes): α- and stable β-phase (at least 15% proportion of weight vanadium); - Quenching to room temperature (i.e. no time for reorganisation of atoms): depending on temperature and cooling rate transformation into metastabile β-phase, soft tcp α - or hard hcp α -Phase; - Microstructure and arrangement of α- and β-phases dependent on heat treatment: lamellar, equiaxed, and a mixture of both.

Titanium Alloy Ti-6Al-4V Microstructures and local stiffnesses of theα- and β-phases in the titanium alloy Ti-6Al-4V: - Determine the macroscopic material behaviour. - Quantitative investigation of the microstructure of titanium alloys after different heat treatments lead to guidelines of systematic material design. - Appropriate tool: Atomic Force Acoustic Microscopy (AFAM). - In addition: energy-dispersive X-ray spectroscopy (EDX) in order to identify the different phases and to determine their chemical composition, backscattered electron (BSE) imaging in order to compare the results with another method.

Titanium Alloy Ti-6Al-4V, AFAM and BSE Images 5 µm khz khz Initial state 5 µm Heat treatment: 650 C (1h), Quenching with water 5 µm 5 µm α-phase: large grains, identification by BSE; β-phase: small dark spots at theα-phase grain boundaries; α-phase: higher contact resonance frequencies and thus higher stiffness than the β-phase; Variation of the stiffness from grain to grain within theα-phase due to the high single crystal anisotropy and different grain orientation. J. Rabe, Diploma thesis, EEIGM, Materialwissenschaft und Werkstofftechnik Fakultät III der Universität des Saarlandes, Saarbrücken, 2009

Titanium Alloy Ti-6Al-4V, AFAM and BSE Images khz Heat treatment: 850 C (1h), Quenching with water 5 µm 5 µm Heating only below the β transition temperature, i.e. the microstructure is mainly determined by hot forming processes, which change structures and induce stresses; the α- and β-phases are present; heating after forming leads to stress reduction and recrystallization, the grain size grows with the temparature of the heat treatment. α-phase: large grains, identification by BSE; β-phase: small dark spots at theα-phase grain boundaries; α-phase: higher contact resonance frequencies and thus higher stiffness than the β-phase; Variation of the stiffness from grain to grain within theα-phase due to the high single crystal anisotropy and different grain orientation. J. Rabe, Diploma thesis, EEIGM, Materialwissenschaft und Werkstofftechnik Fakultät III der Universität des Saarlandes, Saarbrücken, 2009

Titanium Alloy Ti-6Al-4V, AFAM Image khz 5 µm Heat treatment at 1050 C (1h): 100% β-phase; Quenching with water: 100% very fine needle-like tcp α -martensite structure, visible in the AFAM, but not in the BSE image. J. Rabe, Diplomarbeit, EEIGM, Materialwissenschaft und Werkstofftechnik Fakultät III der Universität des Saarlandes, Saarbrücken, 2009

Titanium Alloy Ti-6Al-4V, AFAM and BSE Images khz 5 µm 5 µm khz 2nd Heat treatment at 650 C, quenching with water 2nd Heat treatment at 850 C, quenching with water 5 µm 5 µm Heat treatment at 1050 C (1h), quenching with water, 2nd heat treatment (1h), quenching with water; Sample 5: long plates of α-phase of high stiffness, intermediate theβ-phase of lower stiffness; Sample 6: larger thickness of α-phase plates because of the larger mobility of the atoms during the heat treatment due to the higher temperature. J. Rabe, Diplomarbeit, EEIGM, Materialwissenschaft und Werkstofftechnik Fakultät III der Universität des Saarlandes, Saarbrücken, 2009

Titanium Alloy Ti-6Al-4V, AFAM and BSE Images khz 2nd Heat treatment at 950 C, quenching with water 5 µm 5 µm Heat treatment at 1050 C (1h), quenching with water, 2nd heat treatment (1h), quenching with water. Sample 7: The temperature of the 2nd heat treatment (950 C) is higher than the martensite transition temperature causing transformation of theβ-phase into theα -martensite structure (of lower stiffness than theα-phase). J. Rabe, Diplomarbeit, EEIGM, Materialwissenschaft und Werkstofftechnik Fakultät III der Universität des Saarlandes, Saarbrücken, 2009

Titanium Alloy Ti-6Al-4V Summary of the results: - AFAM and BSE images: consistent, but in contrary to BSE, AFAM clearly shows stiffness variations of different grains in the α-phase due to its strong single crystal anisotropy and different grain orientations as well as the fine needle-like structure of the α -martensite-phase. - Energy-dispersive X-ray spectroscopy (EDX): the chemical composition of the α-phase and thus its lattice parameters and elastic moduli are almost independent on the heat treatment; this is not the case in theβ-phase. - The macroscopic behaviour of Ti-6Al-4V is mainly determined by the ratio of the phases, but not by the chemical composition of the β-phase: AFAM measurements indicate an increasing indentation modulus of the β-phase with decreasing amount of vanadium while ultrasonic bulk measurements show a decreasing macroscopic modulus with increasing temperature. - Investigating microscopic properties as function of heat treatments leads to "material design".