This study reports the high temperature erosion-oxidation (E-O) behavior of conventional and nanostructured Cr3C2-25(Ni-20Cr) coatings prepared by high velocity oxygen fuel (HVOF) spraying. As-received and nanostructured Cr3C2-25(Ni-20Cr) powders with mean crystallite sizes of 145 nm and 50 nm respectively, were used to prepare 120 - 200 µm thick coatings on AISI 310 samples. The E-O behavior of the coatings prepared with the as-received (AR) and nanostructured (NS) powders was determined as weight change in a custom designed rig at room temperature, 450, 700 and 800 ºC. The Vickers microhardness, Young's Modulus and fracture toughness of the AR and NS coatings were determined, and the NS coatings exhibited higher values compared with the AR coatings. The E-O resistance of the NS coating was higher than that of AR coating at all temperatures, and particularly at 800 ºC. The increase in E-O resistance of the NS coatings is due to its superior mechanical properties as well as to the presence of some heterogeneities in the AR coatings. The E-O mechanisms of both types of the coatings are discussed, with special attention to that at high temperatures. The results suggest that at 800 ºC the E-O process is controlled by erosion of the oxide.

Long term isothermal and cyclic oxidation behavior of yttrium dioxide (Y2O3) coated Fe-20Cr alloy was studied. Oxidation tests were carried out in air for periods of up to 200 hours at 1000°C and the oxidation behavior of the alloy was evaluated gravimetrically. The Y2O3 coating reduced markedly the mass gain of the alloy. Energy dispersive spectroscopic analysis of scale sections on oxidized Y2O3 coated specimens revealed a Cr rich layer close to the metal/oxide interface and the presence of Y and Cr near the oxide/air interface, indicating diffusion of Cr through the Y2O3 layer. Further evidence of this diffusion was seen as change in colour of the Y2O3 coating from white to green after prolonged oxidation. X-ray diffraction analysis of the scale revealed perovskite-type YCrO3.This study attributes the increased oxidation resistance of the Y2O3 coated Fe-20Cr alloy to increased oxygen ion diffusion through the Cr2O3 scale due to YCrO3 formation and grain boundary segregated Y ion blocking alloy cation diffusion.

Pitting corrosion of the aluminium cladding of spent nuclear fuels stored in light water pools has been observed. To prevent this, coating of the Al cladding with hydrotalcite (HTC) was proposed. This paper presents the effect of chemical bath and processing parameters on microstructure and corrosion behavior of HTC coatings on alloy AA 6061 specimens. The HTC coating from the high temperature nitrate bath was homogeneous, thicker and consisted of well-defined intersecting platelets than that formed from the room temperature carbonate bath. Electrochemical polarization tests carried out with HTC coated AA 6061 specimens in 0.01 M NaCl revealed that specimens coated with HTC from the nitrate bath and further treated in a cerium salt solution were the most resistant to corrosion. Field tests in which un-coated and coated AA 6061 alloy coupons as well as full-size plates were exposed to the IEA-R1 reactor's spent fuel basin for duration of up to 14 months further corroborated the high corrosion resistance imparted by the high temperature HTC + Ce coating. The mechanism by which the HTC coating and cerium protect the Al alloy is discussed.

A variety of metallic components rely on properties that are specific to the alloy and its surface. Coatings have been extensively used to protect metallic surfaces from the aggressive effects of the environment to which it is exposed. In this investigation, the high temperature oxidation behavior of a FeCr and a FeCrY alloy coated with an aluminium based paint has been studied. The objective was to form the more resistant alumina surface layer on an aluminium free alloy. Aluminium based paint coated and uncoated specimens of the two alloys were oxidized for up to 200 hours at 1000 °C in air. The oxidized specimens were examined in a scanning electron microscope coupled to an energy dispersive system and the surfaces were analyzed by X ray diffraction analysis. The aluminium based paint coating increased the oxidation resistance of the alloys, mainly over extended periods. The FeCrY alloy coated with the Al based paint exhibited the highest oxidation resistance.

Cr3C2-Ni20Cr coatings have been used for corrosion and wear resistant applications. However, one of the shortcomings of these coatings is its low hardness, and consequent low wear resistance, for long term high temperature applications. Nanostructured coatings of many materials have exhibited higher hardness and strength compared with conventional coatings of the same material. Consequently, nanostructured coatings of other materials, including Cr3C2-Ni20Cr have been attempted to enhance overall performance. In this study the effects of high energy milling parameters on Cr3C2-25(Ni20Cr) powder characteristics as well as the microstructure and mechanical properties of nanostructured Cr3C2-25(Ni20Cr) coatings formed by high velocity oxygen fuel (HVOF) spraying have been evaluated. The average particle size and crystallite size of milled Cr3C2-25(Ni20Cr) powders decreased with increase in milling time and this decrease was more pronounced in nitrogen compared to that in hexane. This difference has been attributed to a cushioning effect in the latter medium. The coatings prepared with milled Cr3C2-25(Ni20Cr) powders had a more uniform microstructure, were harder and had higher relative fracture toughness compared with coatings prepared with as-received powders.

The high temperature oxidation and erosion-oxidation (E-O) behavior of steels AISI 1020, 304, 310, and 410 were determined. These steels were selected to evaluate the effect of chromium content on its E-O resistance. The oxidation behavior was determined in a thermogravimetric analyzer. A test rig in which a specimen assembly was rotated through a fluidized bed of erodent particles was used to determine the E-O behavior. Alumina powder (200 µm) was used as the erodent. The E-O tests were carried out in the temperature range 25-600 °C, with average particle impact velocities of 3.5 and 15 ms-1 and impact angle of 90°. The oxidation resistance of the steels increased with chromium content. The E-O behavior of the steels was determined as wastage. The E-O wastage of the steels exposed to particle impact at low velocity was low but increased with temperature above 300 °C. The E-O wastage of the different steels exposed to particle impact at high velocity was quite similar. The wastage increased with increase in temperature above 500 °C. The increases in E-O wastage of the steels observed at temperatures above 300, 400 or 500 °C, depending on the steel, were due mainly to a transition in the dominant wastage process, from 'erosion' to 'erosion-oxidation'.

Rare earths (RE) have been used to increase high temperature oxidation resistance of chromium dioxide and alumina forming alloys. The RE can be added as elements (or oxides) to the alloys or applied as an oxide coating to the alloy surface. RE oxide gels, obtained by the sol-gel technique, were used to coat Fe-20Cr specimens prior to cyclic oxidation tests in the temperature range RT-900 °C. The cyclic oxidation resistance of the alloy increased with time required to reach a specific chromium dioxide layer thickness, and this was influenced by RE ion radius, the coating morphology and coverage. Extended cyclic oxidation tests from peak temperatures of 900, 1000 and 1100 °C at cooling rates of 330 and 1000 °C/s revealed the marked influence of La2O3 coatings. The role of RE in increasing overall oxidation resistance of chromium dioxide forming alloys is discussed.

Doped lanthanum chromite has been used in solid oxide fuel cell (SOFC) interconnects. The high costs involved in obtaining dense lanthanum chromite have increased efforts to find suitable metallic materials for interconnects. In this context, the oxidation behavior of lanthanum chromite coated Fe-20Cr and Fe-20Cr-4Al alloys at SOFC operation temperature was studied. Isothermal oxidation tests were carried out at 1000 °C for 20, 50 and 200 hours. Cyclic oxidation tests were also carried out and each oxidation cycle consisted of 7 hours at 1000/°C followed by cooling to room temperature. The oxidation measurements and the results of SEM/EDS as well as XRD analyses indicated that lanthanum chromite coated Fe-20Cr and Fe-20Cr-4Al alloys were significantly more resistant to oxidation compared with the uncoated alloys.

AISI 304L stainless steel powder compacts containing 2 vol% high purity rare earth oxides were prepared by mixing the different powders in a vibratory mill followed by pressing. The compacts thus obtained were sintered in a vacuum furnace and isothermal oxidation measurements were carried out in a muffle furnace, in air, up to 200 hours at 900 °C. The oxidized surfaces were examined in a scanning electron microscope and micro regions of the reaction products were studied using energy dispersive analysis. The addition of rare earth oxides decreased the oxidation rate of the stainless steel. Further evidence of predominant oxygen ion diffusion controlling the overall oxidation process in rare earth containing chromium oxide forming alloys has been observed.

Rare earths have been used to increase high temperature oxidation resistance of many chromium dioxide and alumina forming alloys. These rare earths can be added as elements (or as oxide dispersions) to the alloys or applied as an oxide coating to the alloy surface. The sol-gel technique is considered to be very efficient to apply fine oxide particle coatings. Oxide gel coatings of various rare earths such as lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, dysprosium, yttrium, erbium and ytterbium have been applied to an iron-chromium alloy to determine their influence on the cyclic oxidation behavior (RT-900 °C) of the alloy. The morphology and coverage of the rare earth oxide gels varied with the type of rare earth. The cyclic oxidation resistance of the alloy increased with increase in time at temperature required to reach a specific chromium dioxide layer thickness and this in turn was influenced by the rare earth ion radius and characteristics of the rare earth oxide coating such as morphology, stability, coverage, resistance to thermal stresses and consequently adhesion.

An apparatus to conduct high temperature erosion-oxidation studies up to 850 °C and with particle impact velocities up to 15 m.s-1 was designed and constructed in the Corrosion Laboratories of IPEN. The erosion-oxidation behavior of high velocity oxy fuel (HVOF) sprayed alloy and cermet coatings of Ni20Cr, WC 20Cr7Ni and Cr3C2 Ni20Cr on a steel substrate has been studied. Details of this apparatus and the erosion-oxidation behavior of these coatings are presented and discussed. The erosion-oxidation behavior of HVOF coated Cr3C2 25(Ni20Cr) was better than that of WC 20Cr7Ni, and the erosion-oxidation regimes have been identified for these coatings at particle impact velocity of 3.5 m.s-1, impact angle of 90° and temperatures in the range 500 to 850 °C.

The addition of small quantities of reactive elements such as rare earths (RE) to chromia or alumina forming alloys improves the high temperature oxidation resistance. Traditionally, these elements are alloying additions or are added as oxides to form a dispersion. The alloys can also be coated with RE oxides. Several methods can be used to coat alloy substrates with RE oxides and the sol-gel process is considered to be quite efficient, as it generates the very small oxide particles. This paper presents the influence of surface coatings of Ce, La, Pr, and Y oxide gels on the oxidation behavior of an Fe-20Cr alloy at 1000 °C. The morphology of the rare earth (RE) oxide coatings varied with the nature of RE. The oxidation rate of RE oxide coated Fe-20Cr was significantly less than that of the uncoated alloy. The extent of influence the RE oxide coating exercised on the oxidation rate decreased in the following order: La, Ce, Pr, Y. The scale formed in the presence of RE oxide was very thin, fine grained and adherent chromia. A direct correlation between rare earth ion radius and the extent of influence on chromia growth rate at 1000 °C was observed.

High temperature corrosion of structural alloys in sulfur bearing environments is many orders of magnitude higher than in oxidizing environments. Efforts to increase sulfidation resistance of these alloys include addition of alloying elements. Aluminum additions to iron-chromium alloys bring about increase in sulfidation resistance. This paper reports the effect of pre-oxidation on the sulfidation behavior of Fe-20Cr and Fe-20Cr-5Al alloys in H2-2% H2S environment at 800 °C. The surfaces of sulfidized specimens were also examined. Pre-oxidation of the two alloys results in an incubation period during subsequent sulfidation. After this incubation period, the Fe-20Cr alloy showed sulfidation behavior similar to that when the alloy was not pre-oxidized. The incubation period during sulfidation of the Fe-20Cr-5Al alloy was significantly longer, over 45 h, compared to 2 h for the Al free alloy. Based on the microscopic and gravimetric data a mechanism for sulfidation of these alloys with pre-oxidation has been proposed.