CMAS corrosion resistance,thermal shock resistance and numerical simulation of novel surface micromesh thermal barrier coatings

Thermal barrier coatings (TBCs) are widely used as insulating layers to protect the underlying metallic structure of gas turbine blades. However, the thermal cycling performance of TBCs is affected by their complex working environments, which may shorten their service life. Previous studies have shown that preparing a mesh structure in the bonding layer can relieve thermal stress and improve the bonding strength, thereby prolonging the service life of TBCs. In this paper, a micromesh structure was prepared on the surface of the bonding layer via wet etching. The microstructure and failure mechanism of the micromesh TBCs after CMAS (CaO-MgO-Al₂O₃-SiO₂) thermal erosion were investigated. Numerical simulation was combined with thermal shock experiments to study the stress distribution of the micromesh-structured TBCs. The results showed that the circular convex structure can effectively improve the CMAS corrosion resistance and thermal shock resistance of TBCs.     

Thermal cycling behavior of EB-PVD rare earth oxides co-doping ZrO2-based thermal barrier coatings

Novel ceramic topcoat of Gd₂O₃–Yb₂O₃–Y₂O₃ co-stabilized ZrO₂ (GYbYSZ) thermal barrier coatings were fabricated via EB-PVD technique. The phase structural stability, phase constituent, chemical composition, morphology and cyclic oxidation of the thermal barrier coatings (TBCs) were systematically studied. Based on the XRD results, the GYbYSZ ceramics has not undergone phase transformation upon long-term annealing at 1373 K and 1523 K. Although the chemical content of the GYbYSZ ceramic coat deviates from the stoichiometric value, the coating is mostly composed of cubic phase, which is accord with the XRD pattern of the original ingot. A pyramidal-like morphology appears in the microtexture of the column tips and the measured diameters of the pyramids are about 2.5~4 μm. After thermal cycling, the surface of the coating presents a multi-layer structure, which is followed by layer-by-layer spallation. The failure zone of the ceramic coats is possible to occur the interior of the thermally grown oxide (TGO) layer, or within the top ceramic coat at the interface of bond coat/TGO layers. The degradation of GYbYSZ TBCs is primarily attributed to the accumulation and relaxation of residual stress, propagation of vertical through microcracks, the growth rumpling of TGO layer, the ridges of grain boundary and the abnormal oxidation of bond coat.     

CMAS corrosion of YSZ thermal barrier coatings obtained by different thermal spray processes

Degradation of yttria-stabilized zirconia (YSZ) layers by molten CaO-MgO-Al₂O₃-SiO₂ (CMAS)-based deposits is an important failure mode of thermal barrier coating (TBC) systems in modern gas turbines. The present work aimed to understand how the chemical purity and microstructure of plasma-sprayed YSZ layers affect their response to CMAS corrosion. To this end, isothermal corrosion tests (1 h at 1250 °C) were performed on four different kinds of YSZ coatings: atmospheric plasma-sprayed (APS) layers obtained from standard- and high-purity feedstock powders, a dense – vertically cracked (DVC) layer, and a suspension plasma sprayed (SPS) one. Characterization of corroded and non-corroded samples by FEG-SEM, EBSD and micro-Raman spectroscopy techniques reveals that, whilst all YSZ samples suffered grain-boundary corrosion by molten CMAS, its extent could vary considerably. High chemical purity limits the extent of grain-boundary dissolution by molten CMAS, whereas high porosity and/or fine crystalline grain structure lead to more severe degradation.     

Microstructural characterization of GZ/CYSZ thermal barrier coatings after thermal shock and CMAS+hot corrosion test

In this study, first, Gd₂Zr₂O₇/ceria–yttria stabilized zirconia (GZ/CYSZ) TBCs having multilayered and functionally graded designs were subjected to thermal shock (TS) test. The GZ/CYSZ functionally graded coatings displayed better thermal shock resistance than multilayered and single layered Gd₂Zr₂O₇ coatings. Second, single layered YSZ and functionally graded eight layered GZ/CYSZ coating (FG8) having superior TS life time were selected for CMAS + hot corrosion test. CMAS + hot corrosion tests were carried out in the same experiment at once. Furthermore, to generate a thermal gradient, specimens were cooled from the back surface of the substrate while heating from the top surface of the TBC by a CO₂ laser beam. Microstructural characterizations showed that the reaction products were penetrated locally inside of the YSZ. On the other hand, a reaction layer having ∼6 μm thickness between CMAS and Gd₂Zr₂O₇ was seen. This reaction layer inhibited to further penetration of the reaction products inside of the FG8.     

Calcium-Magnesium-Aluminosilicate (CMAS) corrosion resistance of high entropy rare-earth phosphate (Lu0.2Yb0.2Er0.2Y0.2Gd0.2)PO4: A novel environmental barrier coating candidate

Single phase (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄ was synthesized, and its thermal properties and CMAS resistance were investigated to explore its potential as an environmental barrier coating (EBC) candidate. The high entropy phosphate (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄ displays a lower thermal conductivity (2.86 W m⁻¹ K⁻¹ at 1250 K) than all the single component xenotime phase rare-earth phosphates. Interaction of (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄ pellets with CMAS at 1300 °C led to the formation of a dense and uniformed Ca₈MgRE(PO₄)₇ reaction layer, which halted the CMAS penetration into the bulk pellet. At 1400 and 1500 °C the (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄-CMAS corrosion showed CMAS penetrating beyond the reaction layer into the bulk pellet via the grain boundaries, and SiO₂ precipitates remaining at the pellet surface. The effects of duration, temperature, and compositions on the resistance against CMAS corrosion are discussed within the context of optimizing materials design and performance of high entropy rare-earth phosphates as candidates for advanced EBC applications.     

Comparison of corrosion behaviors and wettability of CMAS on Ta2O5-Y2O3 co-stabilized ZrO2 and YSZ thermal barrier coatings

High-temperature degradation of the plasma sprayed 16 mol% TaO_2.5 + 16 mol% YO_1.5 co-stabilized ZrO₂ (YTZ) and YSZ (7.6 wt% Y₂O₃-stabilized ZrO₂) coatings under calcium-magnesium-aluminon-silicate (CMAS) attack at 1200 °C and 1250 °C were comparatively investigated. Results indicated that the coatings were insensitive to the infiltration of CMAS after 10 h corrosion at 1200 °C. At 1250 °C, the entire YSZ cross-section completely failed and also underwent serious chemical corrosion after 3 h hot corrosion. Even after 10 h corrosion, the penetration depth of CMAS into the YTZ was only about 80 µm. For YTZ coating, the YTaO₄ stabilizer could not easily dissolve in CMAS and precipitated out of the YTZ crystal lattice owing to the strong chemical interaction between Ta⁵⁺ and Y³⁺. The wettability of CMAS on YTZ coating was worse than that on YSZ coating. Compared with YSZ coating, the YTZ coating showed better resistance to CMAS corrosion.     

Lanthanum magnesium hexaluminate thermal barrier coatings with pre-implanted vertical microcracks: Thermal cycling lifetime and CMAS corrosion behaviour

Atmospheric plasma-sprayed (APS) coatings have a layered structure as well as lower strain tolerance and a shorter lifetime than EB-PVD coatings. In this study, TBCs composed of a LaMgAl₁₁O₁₉ (LMA) top coat and a NiCrAlY bond coat were prepared by APS coupled with dry-ice blasting to implant vertical microcracks in the top coat. The thermal cycling lifetime and CMAS corrosion behaviour of LMA-TBCs with pre-implanted vertical microcracks were investigated in detail. The results show that the LMA top coat possesses an improved proportion of vertical microcracks and that the corresponding TBC has an improved thermal cycling lifetime. The vertical microcracks in the top coats, which not only reduce the thermal stress but also improve the strain tolerance of TBCs, dramatically contribute to the improvement in the thermal cycling lifetime. Surprisingly, the CMAS corrosion resistance of LMA-type TBCs with implanted vertical microcracks is better than that of conventional TBCs with a typical layered structure.     

Plasma sprayed nanostructured GdPO4 thermal barrier coatings: Preparation microstructure and CMAS corrosion resistance

Nanostructured GdPO₄ thermal barrier coatings (TBCs) were prepared by air plasma spraying, and their phase structure evolution and microstructure variation due to calcium–magnesium–alumina–silicate (CMAS) attack have been investigated. The chemical composition of the coating is close to that of the agglomerated particles used for thermal spraying. Nanozones with porous structure are embedded in the coating microstructure, with a percentage of ~30%. CMAS corrosion tests indicated that nanostructured GdPO₄ coating is highly resistant to penetration by molten CMAS at 1250°C. Within 1 hour heat treatment duration, a continuous dense reaction layer forms on the coating surface, which are composed of P–Si apatite based on Ca_2+xGd_8?x(PO₄)_x(SiO₄)_6?xO₂, anorthite and spinel phases. This layer provides effective prevention against CMAS further infiltration into the coating. Prolonged heat treatment densifies the reaction layer but does not change its phase composition.     

Crystallization behavior of CMAS and NaVO3+CMAS mixture and its potential effect to thermal barrier coatings corrosion

Calcium-magnesium-alumina-silicate (CMAS) and molten salt corrosion pose great threats to thermal barrier coatings (TBCs), and recently, a coupling effect of CMAS and molten salt has been found to cause even severer corrosion to TBCs. In this study, the crystallization behavior of CMAS and CMAS+NaVO₃ is investigated for potentially clarifying their corrosion mechanisms to TBCs. Results indicated that at 1000 °C and 1100 °C, CMAS was crystallized to form CaMgSi₂O₆, while at 1200 °C, the crystallization products were CaMgSi₂O₆, CaSiO₃ and CaAl₂Si₂O₈. The introduction of NaVO₃ in CMAS reduced the crystallization ability, and as the NaVO₃ content increased, glass crystallization occurred at a lower temperature, with crystallization products mainly consisting of CaAl₂Si₂O₈ and CaMgSi₂O₆. At 1200 °C, CMAS+10 wt% NaVO₃ was in a molten state without any crystallization, which suggested that NaVO₃ addition in CMAS could reduce its melting point, indicating enhanced penetration ability in TBCs and thus increased corrosiveness.     

Preparation of nanostructured Gd2Zr2O7-LaPO4 thermal barrier coatings and their calcium-magnesium-alumina-silicate (CMAS) resistance

Nanostructured 30 mol% LaPO₄ doped Gd₂Zr₂O₇ (Gd₂Zr₂O₇-LaPO₄) thermal barrier coatings (TBCs) were produced by air plasma spraying (APS). The coatings consist of Gd₂Zr₂O₇ and LaPO₄ phases, with desirable chemical composition and obvious nanozones embedded in the coating microstructure. Calcium-magnesium-alumina- silicate (CMAS) corrosion tests were carried out at 1250 °C for 1–8 h to study the corrosion resistance of the coatings. Results indicated that the nanostructured Gd₂Zr₂O₇-LaPO₄ TBCs reveals high resistance to penetration by the CMAS melt. During corrosion tests, an impervious crystalline reaction layer consisting of Gd-La-P apatite, anorthite, spinel and tetragonal ZrO₂ phases forms on the coating surfaces. The layer is stable at high temperatures and has significant effect on preventing further infiltration of the molten CMAS into the coatings. Furthermore, the porous nanozones could gather the penetrated molten CMAS like as an absorbent, which benefits the CMAS resistance of the coatings.     

Tailoring thermal and mechanical properties of rare earth niobates by coupling entropy and composite engineering

In this paper, a series of high-entropy rare earth niobates, including fluorite RE₃NbO₇ (HE317), monoclinic RENbO₄ (HE114) and RENbO₄/RE₃NbO₇ composite (HE-composite), are prepared via solid state reaction, following by a study about their thermal and mechanical properties. The high-entropy rare earth niobates exhibit excellent phase stability after thermally exposed to 1300 °C for 100 h, indicating entropy can stabilized high-entropy rare earth niobates. Compared with the single element rare earth niobates, high-entropy rare earth niobates have higher fracture toughness and hardness. The high-entropy RENbO₄/RE₃NbO₇ composite has the best mechanical properties, with a fracture toughness of 2.71 ± 0.17 MPa·m^1/2 and hardness of 9.46 ± 0.24 GPa, respectively. The high-entropy niobates exhibit high coefficients of thermal expansion which is close to 7 wt% Y₂O₃ stabilized ZrO₂. It is also proved that the configurational entropy has little effect on the critical temperature from monoclinic to tetragonal phase transition. The thermal conductivity of HE-composite is lower than HE114, indicating the combination of HE114 and H317 is a more efficient strategy to decrease the thermal conductivity of HE114 than entropy engineering.     

The mechanical and thermal properties,CMAS corrosion resistance,and the wettability of novel thermal barrier material GdTaO4

Because the CMAS corrosion and phase transformation at elevated temperatures above 1250 °C have limited the applications of traditional YSZ, the design of novel thermal barrier materials is a hotspot. GdTaO₄ is considered as a type of potential novel thermal barrier material owing to its low thermal conductivity. In this study, the mechanical and thermal properties, CMAS corrosion resistance, and the wettability of the GdTaO₄ were studied and compared with that of YSZ. The results show that the coefficient of thermal expansion and hardness of GdTaO₄ are 14.1 × 10⁻⁶ K⁻¹ (1350 °C) and 534.2 Hv_0.3 respectively. The thickness of CMAS reaction layer of GdTaO₄ is ~30.8 μm after 24 h reaction at 1350 °C, which is thinner than that of YSZ. After corrosion reaction, the CMAS glass aggregated instead of completely disappearing or continuously extending over the surface of GdTaO₄. The main reaction product is Ca₂Ta₂O₇, and the anorthite phase may not be detected, which is similar to YTaO₄. By comparison, the dense substrate of YSZ became porous and CMAS glass has disappeared after 10 h. CMAS corrosion at 1350 °C. The on-line contact angle results show that the wettability of CMAS on GdTaO₄ is worse than that on YSZ at 1350 °C, while the opposite of the work of adhesion, which indicates that GdTaO₄ can remove liquid CMAS more easily than YSZ TBCs during the service. Furthermore, the corrosion depth and areas of GdTaO₄ are smaller than those of YSZ in the same situation. These findings suggest that GdTaO₄ possesses better high-temperature properties and CMAS corrosion resistance than YSZ as a kind of potential of thermal barrier material.     

Hot corrosion studies of nanostructured gadolinium zirconate thermal barrier coatings

Improvement of hot corrosion resistance is one of the important parameters governing the lifetime and efficiency of the thermal barrier coatings (TBCs). In this study, the Gadolinium Zirconate (GZ) was synthesized by ball milling method and deposited by Electron Beam-Physical Vapour Deposition (EB-PVD) on Ni-based superalloy substrate with NiCrAlY as an intermediate bond coat. The effect of nanostructured GZ TBCs on hot corrosion resistance were studied under three different salt mixture environments viz; SM1, SM2 and SM3 in isothermal condition at 900 °C for 12 h. The results indicated that EB-PVD coated nanostructured GZ TBCs have improved the hot corrosion resistance and performed well under SM1 and SM3 conditions with minimal weight gain and without any spallation, whereas, the TBC suffered severe spallation under of SM2 salt condition with higher weight gain among the other two conditions. The formation of microcracks along the columnar gaps of the topcoat were found in the SM2 condition, have allowed the molten salts infiltration up to the coating interface. The formation of dense corrosive products GdVO₄ and m-ZrO₂ phases were identified after hot corrosion in SM1 and SM3 condition, which were absent in SM2 condition.     

Microstructure evolution of CMAS glass below melting temperature and its potential influence on thermal barrier coatings

CaO–MgO–Al₂O₃–SiO₂ (CMAS) deposition significantly degrades the performance of thermal barrier coatings (TBCs). In this study, the microstructure evolution of CMAS glass at temperatures below its melting point was investigated in order to study the potential influence of temperature on the applicability of CMAS glass in TBCs. The CMAS glass fabricated in this study had a melting point of 1240 °C, became opaque, and underwent self-crystallization when the temperature reached 1000 °C. After heat treatment at 1050 °C, diopside and anorthite phases precipitated from the glass; at a higher temperature (1150 °C), diopside, anorthite, and wollastonite were formed as the self-crystallization products. An increase in the dwelling time resulted in the transformation of diopside to wollastonite and anorthite. At 1250 °C, all products formed a eutectic microstructure and melted. The results indicate that even at low temperatures, CMAS glass underwent microstructure evolution, which could influence the coating surface and stress distribution when deposited on TBCs.     

Improvement of corrosion resistance of magnesium metal by rare earth elements

Mg metal containing rare earth metals (REs) can be electrowon directly by molten salt electrolysis. The clarification of the optimum RE content in Mg is necessary to fix the electrolytic conditions in the direct electrowinning of Mg with RE. From this point of view, effect of RE addition in Mg metal on its corrosion property was studied in detail in this study. The specimen was prepared by adding La, Nd, or Ce in melted Mg metal, and its corrosion resistance was examined by an immersion test in 3 mass%-NaCl solution at room temperature. The corrosion resistance of Mg was improved greatly by adding a small amount of RE, whereas the excess addition of RE deteriorated the corrosion resistance. The optimum RE content was about 0.5 mass%. In this study, the corrosion property of Mg with an artificial surface oxide layer was also studied to clarify the effect of surface oxide. The corrosion resistance of Mg was particularly strengthened by conversion coating in a solution including La(NO₃)₃, Nd(NO₃)₃, or Ce(NO₃)₃, with Mg(NO₃)₂. This result suggests that the surface oxide film consisting of both Mg and RE gives ideal corrosion resistance to Mg metal. Mg metal with conversion coating including RE should also be of use as a corrosion-resistant material.     

Thermo-mechanical properties and CMAS resistance of (Ho0.4Yb0.3Lu0.3)2SiO5 solid solution for environmental barrier coating applications

Rare earth monosilicate (RE₂SiO₅) is one of the most promising candidates as an environmental barrier coating (EBC) for SiC_f/SiC ceramic matrix composites. But single-component RE₂SiO₅ is hard to meet the multiple and harsh performance requirements of EBC which brings a significant challenge to their applications. Based on our previous research on single-component RE₂SiO₅ ceramics, (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ solid solution was designed and successfully fabricated in this work. Doping of multiple RE elements endows (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ with excellent thermal insulation properties and matched thermal expansion coefficient with SiC_f/SiC substrates. In addition, it exhibits lower elastic modulus and comparable hardness than that of single-component RE₂SiO₅. (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ also presents good resistance to calcium-magnesium alumino-silicates (CMAS) corrosion. Rational composition design allows (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ to retain the merits of single-component RE₂SiO₅ while taking advantage of the solid solution effect. The results of this work suggest (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ as a promising EBC candidate.     

Microstructural study and hot corrosion behavior of bimodal thermal barrier coatings under laser heat treatment

In this study, nanostructured YSZ powders were deposited on the Hastalloy X Superalloy substrate coated with a metallic bond coat by plasma spraying to produce a nanostructured thermal barrier coating with bimodal microstructure. After that, the coated samples were heat-treated using a Nd:YAG laser. Then, the microstructures of the conventional and nanostructured TBCs before and after the laser glazing process were examined using a scanning electron microscope (SEM). The coating phases were studied by X-ray diffractometry (XRD). The high-temperature corrosion behavior of the nanostructured plasma sprayed coating in the presence of Vanadium pentoxide and Sodium sulfate molten salt was compared with that of the conventional coatings before and after laser treatment at 1050 °C. The hot corrosion results showed that the coatings had a similar degradation mechanism based on which the corrosive molten salt reacted with the stabilizer of YSZ, producing hot corrosion products such as YVO₄. It led to an unwanted phase transformation from tetragonal (t) to monoclinic (m) Zirconia and the final degradation of the TBC system. However, reducing molten salt penetration, decreasing surface roughness and, reduction of the specific surface area are three important mechanisms that improved hot corrosion resistance, finally extending the lifetime of the glazed samples. The results also showed that the nanostructured TBC had higher hot corrosion resistance in comparison with other samples.     

Characterization of stress in a thermal barrier coating during CMAS corrosion using Ce3+ photoluminescence spectroscopy

The stress caused by calcium–magnesium–alumino–silicate (CMAS) corrosion is a critical factor in thermal barrier failure of thermal barrier coatings (TBCs). For the service safety of TBCs, it is important to characterize the stress inside TBCs during CMAS corrosion using a nondestructive and accurate method. In this study, photoluminescence spectroscopy technology was applied to characterize the stress in TBCs during CMAS corrosion. First, TBC specimens containing yttrium–aluminum–garnet doped with trace Ce³⁺ ions (YAG:Ce³⁺)/yttrium oxide partially stabilized zirconia double-ceramic-layer were prepared by atmospheric plasma spraying. Then, CMAS corrosion experiments were performed using the TBC specimens, and a mechanical model was derived based on Ce³⁺ photoluminescence spectroscopy to investigate the stress in the TBCs. Finally, the microstructure, extent of CMAS corrosion and stress field in TBC specimens, was characterized. The results reveal that the penetration of CMAS leads to local stress concentration and a nonlinear stress distribution from the outside surface to the inside of the YAG:Ce³⁺ layer. In addition, an increase in corrosion time, temperature, and CMAS concentration can significantly influence the evolution of the stress field in TBCs.     

Influence of rare earth oxides on kinetics and reaction mechanisms in CMAS silicate melts

Dissolution of different rare earth oxides RE₂O₃ and cyclosilicate Ca₃RE₂(Si₃O₉)₂ was studied at 1200 °C in a pseudo-ternary CAS melt. This investigation is relevant to CMAS resistant thermal barrier coatings (TBC) used in aircraft engines. CMAS is a generic term for the molten siliceous deposits resulting from the ingestion of mineral particles with the intake air. The aim was to assess the influence of the rare earth on the reaction kinetics, solubility limits and underlying phase equilibria in a model CAS melt. RE₂O₃ (RE = Nd, Sm, Gd, Dy and Yb) were selected to span a wide range of trivalent lanthanide sesquioxides and Lewis basicities. Powders dispersed in CAS glass-beads were reacted at 1200 °C and quenched after several durations. All the RE₂O₃ led to the formation of metastable apatite, and then to stabilization of cyclosilicate in CAS. Disilicate Yb₂Si₂O₇ was also obtained in Yb₂O₃ bead-sample during early-stage of interaction. However, RE₂O₃ oxide basicity has a direct influence on silicates (apatite, disilicate and cyclosilicate) solubility limits in CAS, on RE-apatite crystal growth as well as on induction time for RE-cyclosilicate nucleation. The results are discussed in the light of crystal chemistry, thermodynamic considerations and RE cation field strength (Z/r²) which is alternative to define oxide basicity.