Thermal shock resistance of FeMnCrAl/Cr3C2-Ni9Al coatings deposited by high velocity arc spraying

FeMnCrAl/Cr₃C₂ and FeMnCrAl/Cr₃C₂-Ni9Al coatings were deposited onto low-carbon steel substrates by high velocity arc spraying. The cross-section and interface microstructures of the coatings were analyzed by optical microscopy (OM). The thermal shock resistance of the coatings was investigated. The characteristics of the coatings after the thermal cycling test were studied by OM, field emission scanning electron microscopy, and energy dispersion spectrometry. The results show that laminated structures with pores, oxide phases, and unmelted particles were found on all the prepared coatings. The FeMnCrAl/Cr₃C₂ coating with a Ni9Al interlayer registered the best thermal shock resistance, which may be attributed to the interdiffusion between the low-carbon steel substrates and the Ni9Al arc-sprayed coating that converted the mechanical bond between the substrates and the coatings to a metallurgical one.     

超音速火焰喷涂Cr3C2/NiCr涂层抗加沙空蚀性分析

采用HVOF技术在1Cr18Ni9Ti不锈钢基体上制备了Cr3C2/NiCr涂层,借助XRD,TEM,SEM等方法分析了涂层的组织形貌及相组成.以1Cr18Ni9Ti奥氏体不锈钢作为对比材料,用磁致伸缩空蚀仪配备扬沙装置测试了涂层在清水以及含沙水中抗空蚀性能.结果表明,涂层呈层状结构,含有未熔颗粒和少量孔隙,涂层由Cr3C2,Cr7C3,Cr23C6及NiCr等相组成;在清水试验中,1Cr18Ni9Ti不锈钢抗空蚀性能良好,与空蚀过程中1Cr18Ni9Ti奥氏体不锈钢产生加工硬化有直接关系;在含沙40 kg/m3试验水中,Cr3C2/NiCr涂层呈现出较好的抗空蚀性能,与涂层自身相组成以及较高硬度有关.Cr3C2/NiCr涂层破坏总是从孔隙等薄弱环节开始,而1Cr18Ni9Ti奥氏体不锈钢的破坏起始于晶界和孪晶界.     

Hot corrosion behavior of detonation gun sprayed Cr3C2–NiCr coatings on Ni and Fe-based superalloys in Na2SO4–60% V2O5 environment at 900 °C

The present work investigates the hot corrosion resistance of detonation gun sprayed (D-gun) Cr₃C₂–NiCr coatings on Superni 75, Superni 718 and Superfer 800 H superalloys. The deposited coatings on these superalloy substrates exhibit nearly uniform, adherent and dense microstructure with porosity less than 0.8%. Thermogravimetry technique is used to study the high temperature hot corrosion behavior of bare and Cr₃C₂–NiCr coated superalloys in molten salt environment (Na₂SO₄–60% V₂O₅) at high temperature 900 °C for 100 cycles. The corrosion products of the detonation gun sprayed Cr₃C₂–NiCr coatings on superalloys are analyzed by using XRD, SEM, and FE-SEM/EDAX to reveal their microstructural and compositional features for elucidating the corrosion mechanisms. It is shown that the Cr₃C₂–NiCr coatings on Ni- and Fe-based superalloy substrates are found to be very effective in decreasing the corrosion rate in the given molten salt environment at 900 °C. Particularly, the coating deposited on Superfer 800 H showed a better hot corrosion protection as compared to Superni 75 and Superni 718. The coatings serve as an effective diffusion barrier to preclude the diffusion of oxygen from the environment into the substrate superalloys. It is concluded that the hot corrosion resistance of the D-gun sprayed Cr₃C₂–NiCr coating is due to the formation of desirable microstructural features such as very low porosity, uniform fine grains, and the flat splat structures in the coating.     

Microstructure and abrasive wear performance of chromium carbide reinforced Ni3Al matrix composite coating

A Ni-Al-Cr₃C₂ welding wire was produced by metal-powder-core technique. When the welding wires were welded on the surface of carbon steel, under the effect of the physical heat of arc, Ni reacted with Al to form Ni₃Al and carbide particles reinforced Ni₃Al matrix composite was formed. Cr₃C₂ was decomposed during welding and dispersed Cr₇C₃ with stripe shape formed, which strengthened the matrix significantly. The Cr₇C₃-Ni₃Al interface has broadened into a zone of interdiffusion and a new phase M₂₃C₆, which indicates that a good bond has been formed. The pin-abrasion wear test showed that the abrasion resistance of Cr₇C₃/Ni₃Al composite is six times higher than that of Stellite12 alloy at room temperature. The good wear resistance of Cr₇C₃/Ni₃Al composite coating can be attributed to large volume fraction of carbides, high hardness, and good phases interface bond.     

Degradation behaviour of ZrO2-Ni/Al gradient coatings in molten Zn

In order to improve the corrosion resistance of metallic materials in molten zinc, ZrO₂-Ni/Al gradient coatings were sprayed on the surface of the Fe-0.35-0.44 wt.% C steel. The corrosion behaviour and corrosion mechanism of the ZrO₂-Ni/Al gradient coatings in molten zinc were studied. The ZrO₂-Ni/Al gradient coatings on the surface of steels prolonged the lifetime of samples and changed the corrosion behaviour of the samples in molten zinc. The lifetime of the ZrO₂-Ni/Al gradient coatings immersed in molten zinc at 620 °C is 28 days, which is 4 times as long as that of the general ZrO₂ coatings. The ZrO₂-Ni/Al gradient coatings were corroded in molten zinc at 620 °C, which was caused by zinc atom diffusing along the crystal boundary and pores of the ZrO₂-Ni/Al gradient coatings, and reacting with Ni/Al particle in the ZrO₂-Ni/Al gradient coatings. The corrosion mechanism of the coatings in molten zinc at 620 °C was crystal boundary corrosion, pitting corrosion and reaction corrosion.     

Preparation and wear performance of NiCr/Cr3C2-NiCr/hBN plasma sprayed composite coating

NiCr clad hexagonal BN powder (NiCr/hBN) was added to NiCr/Cr₃C₂ feedstock to improve the tribological properties of chromium carbide nichrome coating. The microstructure, flowability and apparent density of the composite powder, as well as the structure and mechanical properties of the plasma sprayed coating were characterized. The friction and wear behavior of the NiCr/Cr₃C₂-NiCr/hBN coating from ambient temperature up to 800 °C was evaluated on a ball-on-disk wear tester and compared with that of NiCr/Cr₃C₂ coating and NiCr/Cr₃C₂-NiCr/BaF₂·CaF₂ coating. The results show that NiCr cladding can reduce the decarburization of Cr₃C₂ and oxidation of hBN during the thermal spray. The main wear mechanisms of the NiCr/Cr₃C₂-NiCr/hBN composite coating are ploughing and adhesive wear. Layered hexagonal BN particle reduce the direct contact and severe adhesion between friction pairs, thus decreasing the friction coefficient. The NiCr/Cr₃C₂-NiCr/hBN composite coating shows a promising application in the high temperature environment with the request of both wear resistance and friction reduction.     

Oxidation of Cr2AlC coatings in the temperature range of 1230 to 1410 °C

The isothermal oxidation behavior of Cr₂AlC coatings on alumina substrates was investigated in the temperature range of 1230 to 1410 °C. The structure, surface morphology, microstructure evolution and chemistry of the reaction products have been investigated. In the investigated temperature range, the Cr₂AlC films form a dense continuous oxide scale consisting of α-Al₂O₃ on Cr carbides. The oxidation rates determined by thermo gravimetric analysis (TGA) were parabolic, indicating that diffusion through the scale is the rate limiting mechanism. The activation energy for oxidation was determined to be 348 kJ mol^− 1 and the parabolic rate constant at 1230 °C was 7.1 × 10^− 10 kg² m^− 4 s^− 1. Hence, the oxidation behavior is comparable to NiAl in the temperature range and time intervals investigated. With increasing oxidation time voids form at the interface between oxide and Cr carbides and the amount of Cr₇C₃ increases at the expense of Cr₃C₂. Based on our thermodynamic calculations the oxygen partial pressure below the oxide scale increases as Al is depleted and Cr carbides oxidize, resulting in CO gas- and Cr₂O₃-formation. The formation of gas may together with the depletion of Al and Cr lead to the significant void formation observed in the Cr carbide interlayer. Observation of both Cr carbide precipitates and the formation of (Al,Cr)₂O₃ solid solution support this notion. For comparison bulk Cr₂AlC was oxidized. It is argued that the absence of pores in oxidized bulk Cr₂AlC is due to the considerably larger amount of Al available.     

热喷涂TiB2-Ni复合涂层组织结构和力学性能

采用团聚烧结方法制备TiB₂-Ni复合粉末喂料,并采用大气等离子喷涂和高速火焰喷涂两种喷涂方法制备了TiB₂-Ni涂层,比较分析了两种涂层的显微组织、物相组成、孔隙率、硬度和断裂韧性.结果表明,与等离子喷涂相比,高速火焰喷涂制备的TiB₂-Ni涂层具有更高的致密度,TiB₂含量,硬度和断裂韧性.两种涂层中TiB₂都没有发生明显的脱硼,氧化,但等离子喷涂过程中TiB₂向金属相中发生了溶解生成了大量脆性Ni₂₀Ti₃B₆相,并降低了涂层中TiB₂的含量,这是涂层硬度和断裂韧性相对较低的主要原因.     

Comparative study of Cr3C2-NiCr coatings obtained by HVOF and hard chromium coatings

In the present work the corrosion resistance of micro-cracked hard chromium and Cr₃C₂-NiCr (HVOF) coatings applied on a steel substrate have been compared using open-circuit potential (E_OC) measurements, electrochemical impedance spectroscopy (EIS) and polarization curves. The coatings surfaces and cross-section were characterized before and after corrosion tests using optical microscopy (OM) and scanning electron microscopy (SEM). After 18 h of immersion, the open-circuit potential values were around −0.50 and −0.25 V/(Ag∣AgCl∣KCl_sat) for hard chromium and Cr₃C₂-NiCr, respectively. The surface analysis done after 12 h of immersion showed iron on the hard chromium surface inside/near surface cracks, while iron was not detected on the Cr₃C₂-NiCr surface even after 18 h. For longer immersion time hard chromium was more degraded than thermal sprayed coating. For hard chromium coating a total resistance values between 50 and 80 kΩ cm² were measured and two well-defined time constants were observed, without significant change with the immersion time. For Cr₃C₂-NiCr coating the total impedance diminished from around 750 to 25 kΩ cm² as the immersion time increased from 17 up to 132 h and two overlapped time constants were also observed. Polarization curves recorded after 18 h of immersion showed a lower current and higher corrosion potential for Cr₃C₂-NiCr coating than other samples studied.     

Effect of alloying with Al on oxidation behavior of MoSi2 coatings at 1100 °C

MoSi₂ - 0, 15.3, 22, and 29.3 at.% Al coatings were prepared on the nickel-based super-alloy substrates by electro-thermal explosion ultrahigh speed spraying technology. The analysis showed that the coatings had fine microstructure with grain sizes ranging from 0.5 to 2 μm. The bonding between coating and substrate was typically metallurgical cohesion. The oxidation resistance of the coating was further studied at 1100 °C in air. Al alloyed in MoSi₂ coatings increased the oxidation resistance of the coatings, and the oxidation resistance of MoSi₂-15.3 at.% Al coating was higher than the other two MoSi₂–Al coatings. This suggested the oxidation resistance might have close relations to the obtained grain size.     

Microstructure and properties of Cr3C2-modified nickel-based alloy coating deposited by plasma transferred arc process

The nickel-based alloy with 30 wt.% chromic carbide (Cr₃C₂) particles has been deposited on Q235-carbon steel (including 0.12 wt.% C) using plasma transferred arc (PTA) welding machine. The microstructure and properties of the deposited coatings were investigated using optical microscope, scanning electron microscope (SEM) equiped with X-ray energy spectrometer (EDS), X-ray diffraction (XRD), transmission electron microscopy (TEM), microhardness testes, and sliding wear test. It was found that the γ(Ni, Fe), M₇(C,B)₃, Ni₄B₃, and (Cr,Fe)₂B phases existed in the Cr₃C₂-free nickel-based alloy coating obtained by PTA process. The typical hypoeutectic structure and composition segregation in the solid solution could be found clearly. The addition of 30 wt.% Cr₃C₂ particles led to the existing of Cr₃C₂ phase and the microstructure changing from hypoeutectic structure into hypereutectic structure. The composition segregation in the solid solution could not be found clearly. The average microhardness of the Cr₃C₂-free nickel-based alloy coating increased by 450-500 HV after the addition of 30 wt.% Cr₃C₂ particles. The partial dissolution of Cr₃C₂ particles led to the enrichment of carbon and chromium in the melten pool, and hence caused the formation of more chromium-rich carbides after the solidification process. The undissolved Cr₃C₂ particles and the increasing of chromium-rich carbides was beneficial to enhance the hardness and wear resistance of the Cr₃C₂-modified nickel-based alloy coating deposited by PTA process.     

Influence of feedstock powder characteristics and spray processes on microstructure and properties of WC-(W,Cr)2C-Ni hardmetal coatings

The composition WC-(W,Cr)₂C-Ni (commercial designations WC-‘CrC’-Ni, WC-Cr₃C₂-Ni and WC-NiCr) is unique among the WC-based materials used for the preparation of thermally sprayed hardmetal coatings. These coatings show a significantly higher oxidation resistance and high-temperature sliding wear resistance than WC-Co and WC-CoCr coatings do. Unlike WC-Co and Cr₃C₂-NiCr, WC-(W,Cr)₂C-Ni is not a simple binary hard phase-binder metal composite as it is composed of two hard phases: WC and (W,Cr)₂C. Surprisingly this composition has been poorly investigated in the past.In this paper coating microstructures and properties obtained from five commercial feedstock powders of different origins using two different liquid-fuelled high velocity oxy-fuel (HVOF) systems (K2 and JP-5000) were investigated. Additional experiments were performed with one powder using atmospheric and vacuum plasma spraying (APS and VPS, respectively). The microstructures and phase compositions of the powders and the coatings were studied. Focus was on the appearance, composition and distribution of the (W,Cr)₂C phase which might form or might change its Cr/W ratio during the spray process. The composition of the (W,Cr)₂C phase was estimated from the lattice parameters. Hardness HV0.3 was measured for all coatings. The density, Young's modulus and abrasion wear resistance of HVOF-sprayed coatings were studied.     

The study of NiAl-TiB2 coatings prepared by electro-thermal explosion ultrahigh speed spraying technology

NiAl-TiB₂ composite coatings with 0, 10 and 20 wt.% TiB₂ were synthesized on the Ni-based superalloy substrate using electro-thermal explosion ultrahigh speed spraying technology. The microstructure analysis shows that the coatings consist of submicron grains. The bond between coatings and substrate is metallic cohesion. TiB₂ as a powerful reinforcement is doped in NiAl for increasing its hardness. The isothermal oxidation test is carried out for the composite coatings at 1100 °C in air. The result shows that the oxidation resistance of NiAl coating is higher than that of NiAl-10TiB₂ and NiAl-20TiB₂ coatings. The phases of oxides on the coatings during the process at high temperature have been analyzed by X-ray diffraction. The results show that Al₂O₃ and Cr₂O₃ coexistence on surface of NiAl coating, while Al₂O₃, Cr₂O₃, TiO₂ and a small amount of NiO form on surface of NiAl-10TiB₂ and NiAl-20TiB₂ coatings after oxidation for 4 h.     

Coke formation and metal dusting of electroplated Ni3Al-CeO2-based coatings in CO-H2-H2O

Coke formation and metal dusting of electrodeposited pure, 5 μm CeO₂-dispersed, and 9-15 nm CeCO₂-dispersed Ni₃Al coatings were investigated in CO-H₂-H₂O at 650 °C for a period of 500 h. All Ni₃Al coatings showed the inferior long-term resistance to coke formation and metal dusting to the Fe-Ni-Cr alloy due to failure to form a continuous Al₂O₃ scale. CeO₂-dispersed Ni₃Al coatings, especially 9-15 nm CeCO₂-dispersed coatings, exhibited more severe coke formation and metal dusting than the pure Ni₃Al coating. The detrimental effect of CeO₂ is believed to be caused by the enhanced formation of NiO/Ni crystals on the coating surfaces or at the grain boundaries, which catalysed the carbon deposition and promoted the carbon attack on Ni₃Al coatings.     

Y2O3 对DZ125合金表面Cr-Al-Y渗层的组织结构及抗氧化性能影响

为进一步提高DZ125合金高温服役性能,通过扩散渗方法在其表面制备了稀土元素Y改性的Cr-Al共渗层,研究了Y₂O₃含量对渗层组织结构及抗高温氧化性能的影响。结果表明：不同条件下制备的Cr-Al-Y渗层均具有三层结构,由外向内依次为：Cr+Ni₃Cr₂外层,Ni₃Cr₂+Al₁₃Co₄中间层,以及Ni₃Al内层。当渗剂中Y₂O₃含量为0%～2%(质量分数,下同)时,渗层的厚度与密度显著增加;当稀土Y₂O₃的添加量过高时(5%),渗层的密度及厚度反而下降。1100℃高温氧化实验表明,Cr-Al-Y渗层显著提高了DZ125合金的抗高温氧化性能。     

激光热喷涂Co30Cr8W1.6C3Ni1.4Si涂层在PAO+2.5%MoDTC油中摩擦学特性

为了提高TC4合金的耐磨性能,采用激光热喷涂技术在其表面制备了Co₃₀Cr₈W_1.6C₃Ni_1.4Si涂层。通过扫描电子显微镜（SEM）和X射线衍射（XRD）分析了涂层的形貌和物相,并通过摩擦磨损实验研究了涂层在PAO+2.5% MoDTC（质量分数）油中的磨损行为。结果表明,激光热喷涂的Co₃₀Cr₈W_1.6C₃Ni_1.4Si涂层主要由Ti、WC_1-x、CoO、Co₂Ti₄O和CoAl相组成,在涂层界面形成冶金结合。在激光功率为1000、1200和1400 W时所制备的涂层平均摩擦因数分别为0.151、0.120和0.171,其对应的磨损率分别为1.17×10^-6、1.33×10^-6和2.80×10^-6 mm³?N^-1?m^-1,磨损机理为磨粒磨损,其枝晶尺寸对降磨起主要作用。     

Microstructure and adhesion of Cr3C2-NiCr vacuum plasma sprayed coatings

Vacuum plasma spraying (VPS) was used to spray a Cr₃C₂-NiCr coating of ∼ 150, 300 and 450 μm in thickness onto a plain carbon steel substrate, employing a commercially available Cr20Ni9.5C powder. The splat microstructures observed in the coating were found to consist of a NiCr matrix with a predominant Cr₃C₂ phase, besides Cr₇C₃ and Cr₂O₃. The adhesion of the coating to the substrate was evaluated by means of interfacial indentation techniques. It has been found that the interfacial toughness value changes from 7.6 to 10.1 MPa m^1/2 when the thickness increases from 150 to 450 μm. Also, it has been found that the parameter Kca_o, determined by linear regression from the Kca versus 1 / e² curve by means of the interfacial indentation model advanced by Chicot et al., has a value of ∼ 9.8 MPa m^1/2.     

Properties of Cr3C2-NiCr cermet coating sprayed by high power plasma and high velocity oxy-fuel processes

The structure, hardness, and shear adhesion strength have been investigated for Cr₃C₂-NiCr cermet coatings sprayed onto a mild steel substrate by 200 kW high power plasma spraying (HPS) and high velocity oxy-fuel (HVOF) processes. Amorphous and supersaturated nickel phases form in both as-sprayed coatings. The hardness of the HVOF coating is higher than that of the HPS coating, because the HVOF coating contains more nonmelted Cr₃C₂ carbide particles. On heat treating at 873 K, the amorphous phase decomposes and the supersaturated nickel phase precipitates Cr₃C₂ carbides so that the hardness increases in the HPS coating. The hardness measured under a great load exhibits lower values compared with that measured with a small load because of cracks generated from the indentation. The ratio of the hardnesses measured with different loads can be regarded as an index indicating the coating ductility. The ductility of the HVOF coating is higher than that of the HPS coating. Adhesion strength of the HVOF coating was high compared with the HPS coating. The adhesion of the coatings is enhanced by heat treating at 1073 K, and that of the HVOF coating is over 350 MPa.     

Effects of Al and Al4C3 contents on combustion synthesis of Cr2AlC from Cr2O3-Al-Al4C3 powder compacts

Preparation of the ternary carbide Cr₂AlC was conducted by combustion synthesis in the mode of self-propagating high-temperature synthesis (SHS) from the Cr₂O₃-Al-Al₄C₃ powder compact. Effects of the contents of Al and Al₄C₃ on the product composition and combustion behavior were studied by formulating the reactant mixture with a stoichiometric proportion of Cr₂O₃:Al:Al₄C₃ = 3:5x:y, where x and y varied from 1.0 to 1.5. When compared to those of the powder compact with Cr₂O₃:Al:Al₄C₃ = 3:5:1 (i.e., x = y = 1.0), the combustion temperature and reaction front velocity increased with content of Al, but decreased with that of Al₄C₃. Besides Cr₂AlC and Al₂O₃, the final products always contained a secondary phase Cr₇C₃ that was substantially reduced by adopting additional Al and Al₄C₃ in the reactant compacts. For the sample with Cr₂O₃:Al:Al₄C₃ = 3:7.5:1 (x = 1.5), solid state combustion reached a peak temperature of 1245 °C and yielded Cr₂AlC with a trivial amount of Cr₇C₃. Although Cr₇C₃ was lessened by introducing extra Al₄C₃, the increase of Al₄C₃ from y = 1.1 to 1.5 produced almost no further reduction of Cr₇C₃ in the final product. This is partly attributed to the low combustion temperature in the range of 1065-1095 °C for the samples with additional Al₄C₃, and in part, due to the role of Al₄C₃ which might react with Cr to form Cr₇C₃, Cr₂Al, and Cr₂AlC.     

Microstructure and Properties of HVOF-Sprayed WC-(W,Cr)<Subscript>2</Subscript>C-Ni Coatings

The composition WC-(W,Cr)₂C-Ni is one of the standard compositions used for the preparation of thermally sprayed coatings by high velocity oxy-fuel (HVOF) spraying. Surprisingly, this composition has been poorly investigated in the past. Frequent use of commercial designations WC-‘CrC’-Ni, WC-Cr₃C₂-Ni, and WC-NiCr indicates the insufficient knowledge about the phase compositions of these powders and coatings. The properties of these coatings differ significantly from those of WC-Co and WC-CoCr coatings. In this paper, the results of different series of experiments conducted on HVOF-sprayed WC-(W,Cr)₂C-Ni coatings are compiled and their specific benefits pointed out. The focus of this study is on the analysis of the microstructures and phase compositions of the feedstock powders and coatings. Unlike WC-Co and Cr₃C₂-NiCr, WC-(W,Cr)₂C-Ni is not a simple binary hard phase—binder metal composite. The phase (W,Cr)₂C with unknown physical and mechanical properties appears as a second hard phase, which is inhomogeneously distributed in the feedstock powders and coatings. As examples of coating properties, the oxidation resistance and dry sliding wear properties are compared with those of WC-10%Co-4%Cr coatings.