Nonplanar microstructures form most frequently during the solidification of alloys, and play a crucial role in governing the properties of the solidified material. This article emphasizes the basic ideas, characteristic lengths, and the processing conditions required to control the columnar and equiaxed microstructures. The formation of cellular and dendritic structures in one- and two-phase structures is presented with emphasis on the effect of processing conditions and composition on the selection of microstructure and microstructure scales.

The process of solidification is the same in all cases, whether it is the freezing of water on a windshield or in a freezer or the solidification of metal in a casting or in the weld that joins two solids. This article discusses the solidification of alloy welds and provides a comparison of casting and welding solidification. The constitutional supercooling model for describing weld solidification is presented because it qualitatively describes the evolution of different weld microstructures. The article describes the welding rate effect on weld pool shape and microstructure, as well as the nonequilibrium effects.

This article discusses the fractal characteristics of fracture surfaces as a means for describing and quantifying irregular, complex curves and surfaces of fractured materials. It describes the important relationship between the profile and surface roughness parameters that yield the surface area of irregular fracture surfaces. The article reviews the experimental procedures required to obtain profiles and measurements that are made. In addition, fractal equations that linearize all the experimental data and provide constant fractal dimensions are presented in the article. Modified fractal dimensions that result from these analyses appear to possess some generality for natural irregular nonplanar surfaces and their profiles.

Triaxial Hopkinson techniques can be used to simultaneously subject a sample to axial and lateral compressions. The lateral compression may be applied through a pneumatic pressure vessel or dynamically using a special Hopkinson technique. This article reviews these two techniques in detail. It illustrates a 75-mm Hopkinson system, particularly designed to test large samples of concrete, rock, polymeric composites, and other materials with relatively coarse microstructures. The article also provides information on the pneumatic pressure vessel for a 75-mm Hopkinson bar test system and the dynamic triaxial load cell on a 19-mm Hopkinson bar.

The principal objective of quantitative fractography is to express the characteristics of features in the fracture surface in quantitative terms, such as the true area, length, size, spacing, orientation, and location. This article provides a detailed account of the development of more quantitative geometrical methods for characterizing nonplanar fracture surfaces. Prominent techniques for studying fracture surfaces are based on the projected images, stereoscopic viewing, and sectioning. The article provides information on various roughness and materials-related parameters for profiles and surfaces. The applications of quantitative fractography for striation spacings, precision matching, and crack path tortuosity are also discussed.

Interdiffusion microstructures appear as a region on either side of the original interface of contact between two materials. This article outlines the principles used in analyzing various interdiffusion microstructures: binary systems, copper-base systems, nickel-base systems, and silicide-forming systems. The analysis can be helpful in classifying microstructures and in understanding how they change with alloy composition, especially when thermal history is known. The microstructures also help in identifying microstructural artifacts caused by polishing and in recognizing errors in reported heat treating schedules.

The quantitative characterization of fracture surface geometry, that is, quantitative fractography, can provide useful information regarding the microstructural features and failure mechanisms that govern material fracture. This article is devoted to the fractographic techniques that are based on fracture profilometry. This is followed by a section describing the methods based on scanning electron microscope fractography. The article also addresses procedures for three-dimensional fracture surface reconstruction. In each case, sufficient methodological details, governing equations, and practical examples are provided.

Sputtering is a nonthermal vaporization process in which the surface atoms are physically ejected from a surface by momentum transfer from an energetic bombarding species of atomic/molecular size. It uses a glow discharge or an ion beam to generate a flux of ions incident on the target surface. This article provides an overview of the advantages and limitations of sputter deposition. It focuses on the most common sputtering techniques, namely, diode sputtering, radio-frequency sputtering, triode sputtering, magnetron sputtering, and unbalanced magnetron sputtering. The article discusses the fundamentals of plasma formation and the interactions on the target surface. A comparison of reactive and nonreactive sputtering is also provided. The article concludes with a discussion on the several methods of process control and the applications of sputtered films.

The development of quantitative fractography (QF) parameters basically requires topological data of a fracture surface that can be derived from the stereological analysis of multiple projected scanning electron microscope (SEM) images; the profilometry-based techniques that measure the fracture surface profile along x-y sections of a fracture surface from metallographic sections or nondestructive techniques; and the three-dimensional reconstruction of the fracture surface topology using imaging methods such as stereo SEM imaging and confocal scanning laser microscopy. These three general methods of assessing fracture surface topology are reviewed in this article.

This article provides information on the typical experimental observations of formation and propagation of small fatigue cracks under various stress states and explores the relation to long crack fracture mixed-mode fracture mechanics. It discusses state I crystallographic and stage II normal stress-dominated growth, along with some observations regarding the influence of combined stress state on the propagation of small cracks. The article discusses the differences between low-cycle fatigue and high-cycle fatigue (HCF) behaviors. Several other features of multiaxial fatigue are also explained, including mean stress effects, sequences of stress/strain amplitude or stress state, nonproportional loading and cycle counting, and HCF fatigue limits. In addition, the article covers the formation and propagation of cracks on the order of several grain sizes in diameter in initially isotropic and ductile structural alloys.

This article demonstrates the depth and breadth of commercial and third-party software packages available to simulate metals processes. It provides a representation of the spectrum of applications from simulation of atomic-level effects to manufacturing optimization. The article tabulates the software name, function or process applications, vendor or developer, and website information.

The metallographic specimen preparation process for microstructural investigations of cast iron specimens usually consists of five stages: sampling, cold or hot mounting, grinding, polishing, and etching with a suitable etchant to reveal the microstructure. This article describes the general preparation of metallographic specimens and the methods of macroscopic and microscopic examination. Usually, gray-scale (black-and-white) metallography is sufficient for microstructural analysis of cast irons. The article discusses the use of color metallography of gray irons and ductile irons. It also presents application examples of color metallography.

Solidification processing is one of the oldest manufacturing processes, because it is the principal component of metal casting processing. This article discusses the fundamentals of solidification of cast iron. Undercooling is a basic condition required for solidification. The article describes various undercooling methods, including kinetic undercooling, thermal undercooling, constitutional undercooling, and pressure undercooling. For solidification to occur, nuclei must form in the liquid. The article discusses the various types of nucleation: homogeneous nucleation, heterogeneous nucleation, and dynamic nucleation. It reviews the classification of eutectics based on their growth mechanism: cooperative growth and divorced growth. The article concludes with a discussion on the solidification structures of peritectics.

This article describes the metallographic specimen preparation procedures for cast iron test samples, including mounting, grinding, polishing, and etching. It discusses the makeup and use of black-and-white and selective color etchants and where one might be preferred over the other. The article provides information on nearly 100 micrographs, discussing the microstructure of flake graphite in gray iron, nodular graphite in ductile iron, and temper graphite in malleable iron. It also examines the matrix microstructures of gray, ductile, compacted, and malleable cast iron samples.

This article provides information on four different length scales at which surface morphology can be viewed: macro, meso, micro and nanoscale. Elementary thermodynamics demonstrates that a liquid cannot solidify unless some undercooling below the equilibrium (melting) temperature occurs. The article details five types of solidification undercooling, namely, kinetic, thermal, constitutional (solutal), curvature, and pressure undercooling. It explains the types of nucleation which occur in the melt during solidification. The effects of local instabilities at the solid/liquid interface during growth are illustrated. The article also describes the solidification structures of pure metals, solid solutions, eutectics, peritectics, and monotectics.

This article reviews the fundamental solidification concepts for understanding microstructural evolution in fusion welds. The common concepts, namely, nucleation, competitive grain growth, constitutional supercooling, solute redistribution, and rapid solidification, depend on the solidification parameters during welding, are discussed. The article discusses important solidification parameters, including temperature gradient, solid/liquid interface growth rate, and cooling rate.

Microscopy is a valuable tool in materials investigations related to problem solving, failure analysis, advanced materials development, and quality control. This article describes the sample preparation techniques of composite materials. These techniques include mounting, rough grinding, and polishing. The preparation techniques of ultrathin sections are also summarized. The article explains the illumination methods used by reflected light microscopy to view a specimen. These consist of epi-bright-field illumination, epi-dark-field illumination, epi-polarized light, and epi-fluorescence. The article also provides information on transmitted light microscopy.

This article discusses the basic operating principles, industrial applications, and advantages as well as the parameters influencing the process of laser-induced forward transfer (LIFT) of solid materials, liquid materials, laser-absorbing layers, intact structures, and metallic 3D microstructures in additive manufacturing.

This article describes how composite specimens are sectioned, documented, and labeled during sample preparation. The mounting procedures for the specimen are summarized. The article explains sample clamping, which involves not mounting the specimens using an adhesive or casting resin and corresponds to clamped samples used in automated polishing heads. It details that cavity molds involve mounting the composite specimens using a casting resin in a preset mold. The article also discusses the mounting of composite materials for hand polishing.

This article describes the various aspects relating to the selection and preparation of ultrathin-section specimens of fiber-reinforced polymeric composites for examination by transmitted light microscopy. It provides information on the contrast-enhancement methods used by transmitted-light microscopy and optimization of microscope conditions. Examples of composite ultrathin sections analyzed using transmitted-light microscopy contrast methods are also presented.