Two types oI zirconia-based thermal barrier coatings (TBCs) were prepared using two diIIerent processes: air plasma spraying (APS) and high-velocity oxygen Iuel (HVOE) top coats were coated onto each bond coat using the APS process. The bond coat thickness plays an important role in limiting the eIIect oI damage.
Two types oI zirconia-based thermal barrier coatings (TBCs) were prepared using two diIIerent processes: air plasma spraying (APS) and high-velocity oxygen Iuel (HVOE) top coats were coated onto each bond coat using the APS process. The bond coat thickness plays an important role in limiting the eIIect oI damage.
Two types oI zirconia-based thermal barrier coatings (TBCs) were prepared using two diIIerent processes: air plasma spraying (APS) and high-velocity oxygen Iuel (HVOE) top coats were coated onto each bond coat using the APS process. The bond coat thickness plays an important role in limiting the eIIect oI damage.
EIIect oI bond coat nature and thickness on mechanical characteristic
and contact damage oI zirconia-based thermal barrier coatings
Jae-Young Kwon a , Jae-Hyun Lee a , Yeon-Gil Jung a, , Ungyu Paik b a School of Nano and Advanced Materials Engineering, Changwon National Universitv, 9 Sarim-dong, Changwon, Kvungnam 641-773, Republic of Korea b Division of Advanced Materials Science Engineering, Hanvang Universitv, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791, Republic of Korea Received 28 March 2006; accepted in revised Iorm 27 July 2006 Available online 7 September 2006 - Mechanical characterization and contact damage oI zirconia-based thermal barrier coatings (TBCs) have been investigated using nanoindentation and Hertzian indentation tests. Two types oI TBC systems with diIIerent bond coat thicknesses oI 60+20 and 280+20 m were prepared using two diIIerent processes: air plasma spraying (APS) and high-velocity oxygen Iuel (HVOE). Top coats were coated onto each bond coat using the APS process. The TBC system with the bond coat Iormed using the HVOE process shows a step-like decrease in mechanical properties on passing Irom the substrate to the top coat, and the bond coat Iormed using the HVOE process indicates higher values oI E and H than that prepared using the APS process. The mechanical properties directly aIIect indentation stressstrain curves oI the TBC systems, and the stressstrain curves oI the TBC system with the APS bond coat are signiIicantly lower than those with the HVOE process. The bond coat thickness plays an important role in limiting the eIIect oI damage, indicating that the thin bond coat enhances contact damage and transmits the damage to the substrate, whereas the thick bond coat limits the damage to within the bond coat at a relatively low load oI P500 N. As the indentation load and the number oI cycles increase, the contact damage is enhanced and becomes more severe in the TBC system with the APS bond coat. The Iracture modes in the top coat and between the top coat and the bond coat oI the TBC system are dependent on the bond coat nature, including the accumulation oI damage and its development at high loads oI 1000 and 1500 N. The TBC system with the APS bond coat shows a bigger and more intensive damage region. 2006 Elsevier B.V. All rights reserved. Kevwords. Bond coat; Plasma spraying; High-velocity oxyIuel (HVOE); Zirconium oxide; Thermal barrier coatings (TBCs)
Zirconia-based thermal barrier coatings (TBCs) on metal alloy substrates are widely used in gas turbines in power generation, and particularly on the Iirst stage oI these gas turbines. Among the various Iabrication methods used Ior TBCs to protect gas turbine blades Irom oxidation and corrosion at high temperatures, the air plasma spraying (APS) process and the electron beam physical vapor deposition (EB-PVD) process have been particularly widely used |18|. APS technology is preIerred commercially in contrast to the use oI complex and expensive EB-PVD equipment, even though EB-PVD coatings have superior properties, such as better corrosion resistance, bond strength, and surIace roughness |9,10|. A bond coat is usually employed in TBCs to improve their structural eIIectiveness and the adhesion between the zirconia- based top coat and the superalloy substrate. In addition, the bond coat plays an important role in protecting the substrate Irom oxidation, having the thickness oI 75150 m|1114|. The bond coat is usually coated onto the substrate using the APS process because oI economic considerations, even though a high number oI deIects, such as pores and microcracks, can occur. However, an increase in the working temperature oI a turbine can lead to service limits oI the TBCs having a bond coat prepared using the APS process. ThereIore, mechanical properties and oxidation resistance oI a bond coat in the TBC system should be enhanced and improved to elongate their liIetime. Recently many techniques Ior Iorming a bond coat have been developed, such as vacuumplasma spraying (VPS), low-pressure plasma spraying (LPPS), high-Irequency pulse detonation (HEPD), and high-velocity oxygen Iuel (HVOE) spraying SurIace & Coatings Technology 201 (2006) 34833490 www.elsevier.com/locate/surIcoat Corresponding author. Tel.: 82 55 289 7201; Iax: 82 55 262 6486. E-mail address. jungygchangwon.ac.kr (Y.-G. Jung). 0257-8972/$ - see Iront matter 2006 Elsevier B.V. All rights reserved. doi:10.1016/j.surIcoat.2006.07.240 |11,1519|. Among these preparation techniques, HVOE spray- ing provides a good microstructure and better adhesive strength, and has low operating coats compared with the APS process, resulting in its replacing the APS process as the Iabrication method Ior Iorming a bond coat in gas turbines. ThereIore, there is a need to estimate and understand the mechanical characteristic and Iracture behavior or damage mode in TBC systems having bond coats prepared using diIIerent processes, such as the APS and HVOE processes, which is essential to improving the reliability and liIetime perIormance oI these TBC systems. The mechanical properties, such as elastic modulus, E, and hardness, H, oI TBCs have been measured using various techniques and reported in the literature, with the Iocus being on zirconia-based top coats |2023|. However, the reported values are inconsistent and dependent on the deIect density in the top coat, such as pores and microcracks, and on geometric Iactors in the measuring method employed. The Iracture behavior and materials response oI layered-structure materials having a plasma- sprayed coating layer Ior contact environments have been developed and well described through model studies, especially in the works oI Lawn et al. |2428|, using the Hertzian contact technique, but the behavior oI real TBC systems has not. The simple Hertzian tests provide quantitative data on indentation stressstrain relationship, and provide qualitative inIormation on the Iracture modes and the evolution oI damage Irom the bonded-interIace technique |24,25|. In this work, the mechanical properties and contact damage oI TBCs with diIIerent bond coats have been evaluated using nanoindentation and Hertzian indentation tests. The relationship between the mechanical properties and the contact damage is discussed, and the advantages oI the HVOE and APS processes Ior Iorming a bond coat in the cyclic contact environments are highlighted.
2.1. Materials and preparation Anickel-based superalloy (GTD-111 developed by the General Electric Company, USA) was used as a substrate. Elat rectangular test samples were machined Irom the shrunken section oI a Iully heat-treated GTD-111 turbine blade using an electro-discharge machining process. Details oI the substrate have been described elsewhere in the literature |20|. The samples were ground and polished to remove the recast layer. Two types oI bond coats were chosen to compare the eIIect oI the bond coat nature and its thickness on the mechanical properties and contact damage in zirconia-based TBCs. One sample was Iormed using the HVOE process with powdered CoNiCrAlYalloy (AMDRTY 4195, Sulzer Metco HoldingAG, Switzerland), and the other coatingwas Iormed using the APS process with powdered CoNiCrAlY alloy (AMDRY 995C, Sulzer Metco Holding AG, Switzerland). Bond coats with two diIIerent thicknesses oI 60+20 and 280+ 20 m were prepared. Top coats were Iormed using powdered zirconia (ZrO 2 ) containing 8 wt. oI yttria (Y 2 O 3 ) (METCO 204NS-G, Sulzer Metco Holding AG, Switzerland), which was air plasma-sprayed to a thickness oI 230+20 monto the bond coats. The Iabrication parameters oI the APS and HVOE processes are shown in Table 1. These are recommended by the manuIacturer. 2.2. Characteri:ation The as-prepared samples were sectioned and given a Iinal polish using 1 m diamond paste Ior characterization. To remove any residual stress induced by the grinding and polishing operations, the samples were Iinally polished with a 10 nm silica (SiO 2 ) colloidal solution. Nanoindentation tests were conducted on each component oI the TBC systems to determine the values oI E and H using a nanoindentor (Nanoinstruments, MTS Systems Corp., Eden Prairie, USA) with a Berkovich tip (tip radius 100 nm), using the continuous stiIIness measurement (CSM) option. The data were selected aIter indentation oI up to 2000 nm depth. Minimum 10 indentations were conducted on each layer-top coat, bond coat, and substrate Ior minimum three samples. Indentation tests using an Instron mechanical properties testing machine (Model 1122, Instron Corp., Canton, MA, USA) employing tungsten carbide (WC) spheres with radius r1.98 9.52 mmwere conducted on the polished top surIaces oI the TBCs with diIIerent types and thicknesses in the bond coat, as well as on the bond coat/substrate without the top coat and on the substrate alone, to obtain indentation stressstrain curves |2428|. The values oI Hand E Ior a WCindenter used in this study are 19 GPa and 614 GPa, respectively |27|. The test surIaces were Iirst polished with 1 mdiamond paste and were then re-polished with a 10 nm silica (SiO 2 ) colloidal solution. AIter indentation, the residual contact radius, a, Ior sphere radius, r, at each applied load was measured, and then indentation stress (p o P/ a 2 ) as a Iunction oI indentation strain, a/r |26,27| was computed. A thin gold coating was deposited on the surIace beIore indentation to help measure the actual contact area at relatively low loads. The bonded-interIace samples polished on both sides were prepared by adhering with cyano-acrylate-based adhesive (Loctite Co., Newington, CT, USA), and then clamped |24,25|. The interIace thickness was below 5 m. The top surIace was slightly polished, and Iinished oII using a 1 m diamond paste beIore clamping. As reIerence specimens, bond coat/substrate samples without the top coat were also prepared Table 1 Starting materials and Iabrication parameters oI the APS and HVOE processes HVOE (Ior bond coat) APS (Ior bond coat) APS (Ior top coat) Material AMDRY 4195 AMDRY 99C METCO 204NS-G Gun JK 3000 Metco 9MB Metco 9MB Primary and secondary gas O 2 and H 2 Ar and H 2 Ar and H 2 Powder carrier gas (psi) Argon (150+2) Nitrogen (40+2) Argon (60+2) Eeed rate (g/min) 35+5 44+5 60+5 Gun-to-work distance (in.) 9+0.5 3+0.5 4+0.5 Gun traverse speed (mm/s) 3+1 5+1 5+1 3484 J.-Y. Kwon et al. / Surface & Coatings Technologv 201 (2006) 34833490 using the HVOE and APS processes. Single-cycle indentations were perIormed on the top surIaces oI the samples using a WC spherical indenter with radius r 3.18 mm up to a peak load oI P1500 N. Normally, the reported compressive residual stresses on thermal barrier coated high pressure turbine blade are 2.42.8 GPa Ior as-prepared and 2.33.1 GPa aIter service, depending on surIace geometry oI thermally grown oxides |29|. ThereIore, we have adjusted the indenter size (WC sphere) Ior the contact tests, based on indentation stressstrain results. In addition, multi-cycle indentations at a peak load oI P500 N were carried out up to 10 6 cycles, and P1000 N up to 10 5 cycles, at a Irequency oI 10 Hz using an Instron cyclic testing machine (Model 8500, Instron Corp., Canton, MA, USA). The indentations were conducted along the trace oI the bonded interIace on the top surIace. The indented specimens were then separated and cleaned, and viewed using an optical microscope. All experiments were perIormed in air at room temperature. -- --- 3.1. Mechanical properties The elastic modulus, E, and hardness, H, oI each component in the TBC systems, which were measured in the nanoindenta- tion tests, are shown in Table 2. The values oI E in the TBC system with the HVOE bond coat show a step-like decrease on passing Irom the substrate to the top coat, whereas the values oI E in the TBC system with the APS bond coat show a sudden decrease on passing through the interIace between the substrate and the bond coat. The values oI H also are not much changed, having a lower value in the bond coat than in the top coat in the TBC system with the APS bond coat. In this study, the changes in E and H at the interIace and the dependence on the bond coat thickness are not considered. The relatively porous microstructure oI the APS bond coat leads to the lower values oI the E and H in the bond coat. The values oI E are changed more dramatically than the values oI H, indicating that the stiIIness is closely related to the microstruc- ture and/or deIects, such as pores and microcracks |21|. A cracking or delamination at the interIace between the bond coat and the top coat will be expected to occur in the indentation tests as the diIIerence in the values oI E and H increases, because oI the elastic/plastic mismatch stress present |20,26|. 3.2. Indentation stressstrain curves Eig. 1 shows indentation stressstrain curves Ior the TBC system with the HVOE bond coat and the HVOE bond coat/ substrate system without the top coat as a Iunction oI the bond coat thickness, and Ior the substrate alone. The system becomes soIter as the bond coat and the top coat are Iormed on the substrate. This result can be expected Irom the values oI E and H in Table 2. The stressstrain curves are not aIIected much by a change in the bond coat thickness, except in the lower and higher stress regions Ior the bond coat/substrate and the top coat/bond coat/substrate systems, respectively. In the bond coat/ substrate system, a compression stress applied to the thin bond coat is constrained in the early stages by the harder substrate, resulting in a smaller contact area in the lower stress region compared with the case oI the thick bond coat. In the top coat/ bond coat/substrate system, the bond coat or the substrate reacts to the compression stress in the higher strain region, resulting in the same response observed Ior the porous microstructure oI the top coat versus the compression stress in the lower strain region. Consequently, the top coat and the bond coat in the TBC systems result in a soItening oI the substrate, with a minor eIIect oI the bond coat thickness on the soItening. The stressstrain curves Ior the APS bond coat are much lower than those prepared using the HVOE process, and this is especially so Ior the thick bond coat (Eig. 2). DeIects, such as pores and microcracks, are accumulated in the bond coat as the bond coat thickness is increased. ThereIore, the stressstrain curves in the bond coat/substrate system with the APS bond coat show a dramatic change with increasing the bond coat thickness. It is interesting to note that the stressstrain curve oI the top coat/bond coat/substrate system is located below that oI the bond coat/substrate system, even though the values oI E and H are slightly higher. The nanoindentation tests provide the values oI E and H in localized regions, which lowers any eIIect oI changes in the microstructure. Previous studies have indicated that the global and local properties oI TBCs show a large scatter in the observed data |21,23,30|. The inIluence oI the hard substrate can be considered as another possibility, because the value oI E oI the substrate is much higher than those oI the top and the bond coat. As a result, the properties oI the Table 2 Elastic modulus, E, and hardness, H, oI the substrate, bond coats, and top coat measured using the nanoindentation technique Properties Substrate (GTD 111) HVOE (Ior bond coat) APS (Ior bond coat) APS (Ior top coat) E (GPa) 232+28 155+21 90+35 94+32 H (GPa) 5.6+0.4 5.0+0.8 3.2+0.9 4.2+0.9 The bond coats were prepared using diIIerent processes: HVOE and APS. Eig. 1. Indentation stressstrain curves Ior substrate, bond coat/substrate, and top coat/bond coat/substrate in the TBC system with the bond coat being prepared using the HVOE process. The data were obtained using WC spheres with r 1.989.52 mm. The solid curves are empirical data Iits. 3485 J.-Y. Kwon et al. / Surface & Coatings Technologv 201 (2006) 34833490 thermal barrier top coat make the system soIter, and this is independent oI the bond coat type. In addition, the stressstrain curves oI the bond coat/substrate system with the APS bond coat are dependent on the bond coat thickness. However, the relatively hard bond coat Iormed by the HVOE process diminishes the soItening eIIect and the eIIect oI the bond coat thickness on the stressstrain curves, which is consistent with the observed mechanical properties. 3.3. Contact damages The eIIect oI the bond coat thickness and the top coat in the TBC system with the HVOE bond coat on the evolution oI contact damage is shown in Eig. 3, which shows micrographs oI the subsurIace damage aIter cyclic indentation tests carried out at a peak load oI P500 N Ior n1, 10 5 , and 10 6 , using a WC spherical indenter with r 3.18 mm. The damage in the substrate is easily developed Irom a single indentation in the TBC system with the thin bond coat, which is extended to a depth limited by the coat. The top coat is disintegrated as the number oI cycles is increased. Meanwhile, the TBC system with the thick bond coat shows a damage zone contained within the bond coat, which is not transmitted to the substrate, even Ior a high number oI cycles, n10 6 . The contact diameter is not much aIIected by diIIerent bond coat thickness, except when a higher number oI cycles, n10 6 , is applied. The subsurIace damage indicates that the thicker bond coat is more eIIicient in protecting the substrate Irom contacts than the thinner bond coat, although indentation stressstrain curves shown in Eig. 1 are similar. The system without the top coat, i.e., the bond coat/ substrate system, also shows a well-deIined damage zone, with Eig. 3. Contact damages oI top coat/bond coat/substrate and bond coat/substrate, at peak load P500 N and Irequency 10 Hz, Ior n1, 10 5 , and 10 6 . (a) and (b) are the top coat/bond coat/substrate Ior bond coat thicknesses oI d 60 and 280 m, respectively, and (c) is the bond coat/substrate Ior bond coat thickness oI d 280 m. The contact diameter is shown by arrows. The bond coats were prepared using the HVOE process. Indentation was carried out using a WC sphere with r 3.18 mm. Eig. 2. Indentation stressstrain curves Ior bond coat/substrate and top coat/bond coat/substrate in the TBC system with the bond coat being prepared using the APS process. The data were obtained using WC spheres with r 1.989.52 mm. The solid curves are empirical data Iits. The dashed curve is the substrate material shown in Eig. 1, and is included Ior comparison. 3486 J.-Y. Kwon et al. / Surface & Coatings Technologv 201 (2006) 34833490 a minor damage occurring in the substrate. The contact diameter oI the bond coat/substrate system is independent oI the number oI cycles, showing a similar contact diameter in all cases. However, the contact diameter oI the bond coat/substrate system is smaller than those oI the top coat/bond coat/substrate systems, consistent with the data shown in Eig. 1, indicating that the top coat is soIter than the bond coat. The damage zone Iormed in the bond coat is not extended, only showing damage accumulation within the bond coat, whereas the damage zone in the thinner bond coat is well deIined within the substrate (results not shown), and this damage is extended into the substrate with increasing the number oI cycles. The subsurIace damage oI the TBC system with the APS bond coat is shown in Eig. 4. The test condition was same with the case oI Eig. 3. In comparison with Eig. 3(c), the damage zone in the bond coat/substrate system reaches the interIace Ior a single indentation, and this is accumulated and is extended with increasing the number oI cycles. An intensive damage zone is developed because oI the soIt bond coat. As mentioned above in the discussion on indentation stressstrain curves, the soIter bond coat will transIer the stress to the substrate and damage the substrate. The top coat acts as a protective layer in a contact environment, showing less damage in the bond coat and no damage in the substrate compared with the case without the top coat. The contact diameter oI the TBC system with the top coat is larger than that oI the TBC system without the top coat, indicating that the hard substrate restrains the development oI contact damage. This result is consistent with the stressstrain curves shown in Eig. 2. The evolution oI damage Ior each case is shown in Eigs. 5 and 6 when the indentation load is increased to P1000 N. Eig. 5 shows micrographs Ior the TBC system with the HOVE bond coat. The damage zone is extended to the substrate to a limited depth Ior a single indentation, and this is independent oI the top coat. The damage zones in both the bond coat and the substrate and the contact diameter are much smaller than those oI the APS process (Eig. 6). Also, the bending oI the bond coat is constrained in the HVOE process. This is due to better mechanical properties conIerred by the HVOE process, which is consistent with the stressstrain data. AIter the cyclic tests, the damage zones and contact diameter oI the TBC system with the HVOE bond coat are smaller than those oI the TBC system with the APS bond coat, indicating that the values oI EandHoI the APS bond coat aIIect the development oI contact damage and the accumulation oI damage. ThereIore, the HVOE bond coat is eIIective in improving the damage tolerance oI the TBCs system. In high magniIication micrographs shown in Eig. 7, the diIIerence between the HVOE and APS processes is particularly apparent. In the TBC system with the HVOE bond coat, crack or delamination at the interIace oI the top coat and the bond coat is apparent, along with a small damage zone in the bond coat. Meanwhile, in the TBC system with the APS bond coat, the Iracture is developed within the top coat and not the interIace. The diIIerence in preparation method oI the top coat and the bond coat in the TBC system with the HVOE bond coat aIIect the Iracture behavior at the interIace between the top coat and the bond coat, according to the diIIerent Iormation behavior Ior each coat. In addition, the damage zone is smaller than that Eig. 4. Contact damages oI (a) bond coat/substrate and (b) top coat/bond coat/ substrate with bond coat thickness oI d 280 m prepared using the APS process, at peak load P500 N and Irequency 10 Hz, Ior n1, 10 5 , and 10 6 . The contact diameter is shown by arrows. Indentation was carried out using a WC sphere with r 3.18 mm. 3487 J.-Y. Kwon et al. / Surface & Coatings Technologv 201 (2006) 34833490 observed Ior the APS process. However, there are no cone-like cracks on the top coat created in the dense and brittle material or vertical cracks at the interIace caused by the soIt substrate |28|. The Iracture mode in the top coat is also dependent on the bond coat type. The Iracture oI the top coat in the TBC system with the harder bond coat (prepared using the HVOE process) arise Eig. 5. Contact damages oI (a) bond coat/substrate and (b) top coat/bond coat/ substrate with bond coat thickness oI d 280 m prepared using the HVOE process, at peak loads P1000 N and Irequency 10 Hz, Ior n1, 10 3 , and 10 5 . The contact diameter is indicated by arrows. Indentation was carried out a WC sphere with r 3.18 mm. Eig. 6. Contact damages oI (a) bond coat/substrate and (b) top coat/bond coat/ substrate with bond coat thickness oI d 280 m prepared using the APS process, at peak loads P1000 N and Irequency 10 Hz, Ior n1, 10 3 , and 10 5 . The contact diameter is indicated by arrows. Indentation was carried out using a WC sphere with r 3.18 mm. 3488 J.-Y. Kwon et al. / Surface & Coatings Technologv 201 (2006) 34833490 because oI the compression on the top coat with less crack coalescence, whereas the Iracture in the TBC system with the soIter bond coat (prepared using the APS process) is due to the mixed mode oI compression on the top coat and bending in the bond coat with larger and more open cracks. Contact damage under a high load P1500 N is shown in Eig. 8, Ior the TBC systems with diIIerent bond coats Iormed using the HVOE and APS processes (Eigs. 8(a) and 8(b), respectively). The damage modes in the bond coat and the substrate oI the TBC system with the HVOE bond coat Iollow the mechanical properties oI each coat and show a gradual transition on passing Irom the top coat to the substrate. The bond coat should Iorm a protection layer against impacts. However, the bond coat with similar mechanical properties to the top coat enhances any damage in the substrate, showing a bigger damage zone in the bond coat. This study shows that a relatively porous bond coat will be advantageous Irom the viewpoint oI energy absorption, especially at low impact loads Ior P 500 N or Ior a lower number oI cycles. However, this structural advantage is diminished at higher loads above P1000 N or Ior a higher number oI cycles, as this enhances the damage and so expands the damage zone in both the bond coat and the substrate. In view oI the liIetime oI the system, a porous structure lessens damage tolerance and accelerates the Iailure oI the system, even though it has been reported that damage accumulated on the top coat or the bond coat can improve the thermal protection oI the substrate |31|. Using the HVOE process Ior the bond coat is the better choice Ior improving damage tolerance and Ior protecting the substrate in TBC systems. In addition, a thicker bond coat has to be applied to a TBC system to protect the substrate Irom impacts. However, a dense microstructure and higher mechan- ical properties lead to a higher degree oI stiIIness, resulting in low thermo-mechanical stability because oI high residual stress and a low strain tolerance during service at high temperature |23,32|. ThereIore, the damage modes and mechanical properties oI the TBC system aIter thermal Iatigue need to be investigated to conIirm the eIIect oI the bond coat on contact damage and to determine the best conditions Ior the bond coat in TBC systems in a real application. These studies are now in progress and will be reported on in a later publication. In this work, two types oI TBCs with diIIerent bond coats prepared using the HVOE and APS processes were prepared to evaluate the eIIect oI the bond coat nature, i.e., HVOE or APS process derived with thicknesses oI 60+20 and 280+20 m, on Iracture behavior and contact damage in air plasma-sprayed zirconia-based TBCs. The mechanical properties oI each componentthe top coat, bond coat and substratein the TBC systems were measured using nanoindentation tests to obtain the elastic modulus, E, and hardness, H. The Hertzian indentation tests provide indentation stressstrain curves Ior each component and TBCs with diIIerent natures and thicknesses in the bond coat. The mechanical properties oI the bond coat are dependent on the preparation method and are consistent with indentation stressstrain curves. The bonded- Eig. 8. Contact damages oI top coat/bond coat/substrate systems with bond coat thickness oI d 280 m prepared using the (a) HVOE and (b) APS processes. Indentation was carried out using a WC sphere with r 3.18 mm and P1500 N, Ior n1. The solid and dotted lines indicate the damaged regions in the bond coat and the substrate, respectively. Eig. 7. High magniIication optical micrographs oI top coat/bond coat/substrate systems with bond coat thickness oI d 280 m prepared using the (a) HVOE and (b) APS processes. Indentation was carried out using a WC sphere with r 3.18 mm, P1000 N, and Irequency 10 Hz Ior n10 5 . 3489 J.-Y. Kwon et al. / Surface & Coatings Technologv 201 (2006) 34833490 interIace samples show an accumulation oI damage and the evolution oI Iracture in the TBC system. These indicate that the bond coat nature and its thickness aIIect the contact damage obtained Irom cyclic contact tests, including the eIIect oI the top coat on the evolution oI damage. -- The mechanical properties, E and H, oI the bond coat are dependent on the preparation process, and show higher values when the bond coat is Iabricated using the HVOE process. The values oI E and H in the TBC system with the HVOE bond coat show a step-like decrease Irom the substrate and the top coat, whereas the values oI the APS bond coat show a sudden decrease on passing through the interIace between the substrate and the bond coat. The values oI E and H are strongly inIluenced by the bond coat nature. In the TBC system with the HVOE bond coat, the stressstrain curves are not much aIIected by the bond coat thickness, except in the lower and higher stress regions oI the bond coat/substrate and the top coat/bond coat/ substrate systems, respectively. Consequently, the top coat and the bond coat result in a soItening oI the substrate, with a resulting lower eIIect oI the bond coat. The stressstrain curves Ior the APS bond coat are much lower that those oI the HVOE process, especially Ior the thick bond coat. However, the relatively hard bond coat Iormed using the HVOE process diminishes the eIIect oI soItening and the thickness, which is consistent with the observed mechanical properties. The subsurIace damage indicates that the thick bond coat is more eIIicient Ior protecting the substrate Irom the contact environment than the thin bond coat. The TBCsystemwithout the top coat, i.e., bond coat/substrate system, also exhibits well- deIined damage within the bond coat, with a minor damage in the substrate, and this represents a larger contact diameter Ior the APS process, but independent oI the number oI cycles. The damage Iormed in the thick bond coat is not extended and the bond coat/ substrate only shows damage that has accumulated within the bond coat at a relatively low load oI P500 N, whereas the damage zone in the thin bond coat is well deIined in the substrate and extended into the substrate with increasing the number oI cycles. The HVOE bond coat is eIIicient in improving the damage tolerance oI the TBC system. The Iracture oI the top coat in the TBCsystemwith the HVOE bond coat is due to compression with less crack coalescence, whereas the Iracture with the APS bond coat is due to the mixed mode oI compression on the top coat and bending in the bond coat with the Iormation oI larger open cracks. The damage mode in the bond coat and the substrate oI the TBC system with the HOVE bond coat Iollows the mechanical properties oI each coat and shows a gradual transition Iromthe top coat to the substrate. The bond coat should act as a protective layer Ior impacts. However, the TBC system with the APS bond coat, which has similar mechanical properties to the top coat, enhances damage in the substrate and shows a bigger damage in the bond coat. - This work was Iinancially supported by MOCIE through an EIRC program, a program Ior cultivating graduate students in regional strategic industry, and Changwon National University in 2005. Thanks are due to Brian Lawn Ior providing continual encouragement during this work. - |1| D.R. Clarke, C.G. Levi, Annu. Rev. Mater. Res. 33 (2003) 383. |2| R.A. Miller, SurI. Coat. Technol. 30 (1987) 1. |3| R.L. Jones, J. Therm. Spray Technol. 6 (1) (1997) 77. |4| B. Siebert, C. Eunke, R. Vaben, D. Stover, J. Mater. Process. Technol. 92 93 (1999) 217. |5| R. Vaben, N. Czech, W. Mallener, W. Stamm, D. Stover, SurI. Coat. Technol. 141 (2001) 135. |6| V. Schulz, M. Schmucker, Mater. Sci. Eng., A, Struct. Mater., Prop. Microstruct. Process. 276 (2000) 1. |7| D.E. WolIe, J. Singh, R.A. Miller, J.I. Eldridge, D.M. Zhu, SurI. Coat. Technol. 190 (2005) 132. |8| S. Guo, Y. Kagawa, Ceram. Inter. 32 (2006) 263. |9| Y. Itoh, M. Saitoh, M. Tamura, J. Eng. Gas Turbine Power 122 (2000) 43. |10| Y.N. Wu, G. Zhang, Z.C. Eeng, B.C. Zhang, Y. Liang, E.J. Liu, SurI. Coat. Technol. 138 (2001) 56. |11| L.B. Ereund, S. Suresh, Thin Eilm Materials, Cambridge University Press, Cambridge, UK, 2003, p. 10. |12| J.R. Brandon, R. Taylor, SurI. Coat. Technol. 69 (10) (1992) 75. |13| A. Bennett, Mater. Sci. Technol. 30 (1987) 1. |14| R.L. Jones, in: K.H. Sterm (Ed.), Metallurgical and Ceramic Coatings, Chapman and Hall, London, 1996, p. 194. |15| M.-P. Bacos, P. Josso, N. Vialas, D. Poquillon, B. Pieraggi, D. Monceau, J.R. Nicholls, N. Simms, A. Encinas-Oropesa, T. Ericsson, S. Stekovic, Appl. Therm. Eng. 24 (2004) 1745. |16| S. Takahashi, M. Yoshiba, Y. Harada, Mater. High Temp. 18 (2001) 125. |17| N.J. Simms, P.J. Kilgallon, C. Roach, J.E. Oakey, Mater. High Temp. 20 (2003) 519. |18| Kh.G. Schmitt-Thomas, H. Haindl, D. Eu, SurI. Coat. Technol. 9495 (1997) 149. |19| E. Tang, L. Ajdelsztain, G.E. Kim, V. Provenzano, J.M. Schoenung, SurI. Coat. Technol. 185 (2004) 228. |20| H.J. Jang, D.H. Park, Y.G. Jung, J.C. Jang, S.C. Choi, U. Paik, SurI. Coat. Technol. 200 (2006) 4355. |21| J.A. Thompson, T.W. Clyne, Acta Mater. 49 (2001) 1565. |22| C.A. Johnson, J.A. Ruud, R. Bruce, D. Wortman, SurI. Coat. Technol. 108 (1998) 80. |23| J. Malzbender, R.W. Steinbrech, J. Mater. Res. 18 (8) (2003) 1975. |24| E. Guiberteau, N.P. Padture, B.R. Lawn, J. Am. Ceram. Soc. 77 (1994) 1825. |25| H. Cai, M.A. Stevens KalceII, B.R. Lawn, J. Mater. Res. 9 (1994) 762. |26| A. Pajares, L. Wei, B.R. Lawn, N.P. Paduture, C.C. Berndt, Mater. Sci. Eng., A, Struct. Mater., Prop. Microstruct. Process. 208 (1996) 158. |27| S. Wuttiphan, A. Pajares, B.R. Lawn, C.C. Berndt, Thin Solid Eilms 293 (1997) 251. |28| A. Pajares, L. Wei, B.R. Lawn, C.C. Berndt, J. Am. Soc. 79 (1996) 1907. |29| Y.H. Sohn, E.Y. Lee, B.A. Nagaraj, R.R. Biederman, R.D. Sisson Jr., SurI. Coat. Technol. 146147 (2001) 132. |30| D. Basu, C. Eunke, R.W. Steinbrech, J. Mater. Res. 14 (1999) 12. |31| L. Wei, A. Pajares, B.R. Lawn, J. Mater. Res. 11 (1996) 1329. |32| N.P. Paduture, M. Gell, E.H. Jordan, Science 296 (2002) 280. 3490 J.-Y. Kwon et al. / Surface & Coatings Technologv 201 (2006) 34833490