Engineered handbook material

SEK Swedish Kroner. BDT Bangladeshi Taka. Environment Engineering. Mechanical Engineering. Electrical Engineering. Engineered Materials Handbook Vol. Send to friend.

Title: Engineered Materials Handbook Vol. About Us Contact us. All rights reserved. Therefore, hardness is important from an engineering standpoint because resistance to wear by either friction or erosion by steam, oil, and water generally increases with hardness.

Hardness tests serve an important need in industry even though they do not measure a unique quality that can be termed hardness. The tests are empirical, based on experiments and observation, rather than fundamental theory.

Its chief value is as an inspection device, able to detect certain differences in material when they arise even though these differences may be undefinable.

For example, two lots of material that have the same hardness may or may not be alike, but if their hardness is different, the materials certainly are not alike.

Several methods have been developed for hardness testing. The first four are based on indentation tests and the fifth on the rebound height of a diamond-tipped metallic hammer. The file test establishes the characteristics of how well a file takes a bite on the material. As a result of many tests, comparisons have been prepared using formulas, tables, and graphs that show the relationships between the results of various hardness tests of specific alloys. There is, however, no exact mathematical relation between any two of the methods.

Another convenient conversion is that of Brinell hardness to ultimate tensile strength. For quenched and tempered steel, the tensile strength psi is about times the Brinell hardness number provided the strength is not over , psi. Nickel is an important alloying element. It will not raise the hardness when added in these small quantities because it does not form carbides, solid compounds with carbon.

Chromium in steel forms a carbide that hardens the metal. The chromium atoms may also occupy locations in the crystal lattice, which will have the effect of increasing hardness without affecting ductility. The addition of nickel intensifies the effects of chromium, producing a steel with increased hardness and ductility.

Copper is quite similar to nickel in its effects on steel. Copper does not form a carbide, but increases hardness by retarding dislocation movement. Molybdenum forms a complex carbide when added to steel. Because of the structure of the carbide, it hardens steel substantially, but also minimizes grain enlargement.

Molybdenum tends to augment the desirable properties of both nickel and chromium. An important characteristic of these steels is their resistance to many corrosive conditions. Heat treatment and working of the metal are discussed as metallurgical processes used to change the properties of metals. Personnel need to understand the effects on metals to select the proper material for a reactor facility.

Heat treatment of large carbon steel components is done to take advantage of crystalline defects and their effects and thus obtain certain desirable properties or conditions. During manufacture, by varying the rate of cooling quenching of the metal, grain size and grain patterns are controlled. Grain characteristics are controlled to produce different levels of hardness and tensile strength. Generally, the faster a metal is cooled, the smaller the grain sizes will be.

This will make the metal harder. As hardness and tensile strength increase in heat-treated steel, toughness and ductility decrease. The cooling rate used in quenching depends on the method of cooling and the size of the metal. Uniform cooling is important to prevent distortion. Typically, steel components are quenched in oil or water. Because of the crystal pattern of type stainless steel in the reactor tank tritium production facility , heat treatment is unsuitable for increasing the hardness and strength.

Welding can induce internal stresses that will remain in the material after the welding is completed. In stainless steels, such as type , the crystal lattice is face-centered cubic austenite. In this temperature region, the austenite is transformed into a body-centered cubic lattice structure bainite. When the metal has cooled, regions surrounding the weld contain some original austenite and some newly formed bainite. The bainite that has been formed occupies more space than the original austenite lattice.

This elongation of the material causes residual compressive and tensile stresses in the material. Welding stresses can be minimized by using heat sink welding, which results in lower metal temperatures, and by annealing. Annealing is another common heat treating process for carbon steel components.

During annealing, the component is heated slowly to an elevated temperature and held there for a long period of time, then cooled. The annealing process is done to obtain the following effects. Plastic deformation which is carried out in a temperature region and over a time interval such that the strain hardening is not relieved is called cold work. Considerable knowledge on the structure of the cold-worked state has been obtained. In the early stages of plastic deformation, slip is essentially on primary glide planes and the dislocations form coplanar arrays.

As deformation proceeds, cross slip takes place. The cold-worked structure forms high dislocation density regions that soon develop into networks. The grain size decreases with strain at low deformation but soon reaches a fixed size. Cold working will decrease ductility. Hot working refers to the process where metals are deformed above their recrystallization temperature and strain hardening does not occur. Hot working is usually performed at elevated temperatures.

Lead, however, is hot-worked at room temperature because of its low melting temperature. At the other extreme, molybdenum is cold-worked when deformed even at red heat because of its high recrystallization temperature.

The resistance of metals to plastic deformation generally falls with temperature. For this reason, larger massive sections are always worked hot by forging, rolling, or extrusion. Metals display distinctly viscous characteristics at sufficiently high temperatures, and their resistance to flow increases at high forming rates.

This occurs not only because it is a characteristic of viscous substances, but because the rate of recrystallization may not be fast enough. Corrosion is a major factor in the selection of material for a reactor plant.

The material selected must resist the various types of corrosion discussed in the Chemistry Fundamentals Handbook. Corrosion is the deterioration of a material due to interaction with its environment.

It is the process in which metallic atoms leave the metal or form compounds in the presence of water and gases. Metal atoms are removed from a structural element until it fails, or oxides build up inside a pipe until it is plugged. All metals and alloys are subject to corrosion. Even the noble metals, such as gold, are subject to corrosive attack in some environments. The corrosion of metals is a natural process.

Most metals are not thermodynamically stable in the metallic form; they want to corrode and revert to the more stable forms that are normally found in ores, such as oxides. Corrosion is of primary concern in nuclear reactor plants.

Corrosion occurs continuously throughout the reactor plant, and every metal is subject to it. Even though this corrosion cannot be eliminated, it can be controlled. General corrosion involving water and steel generally results from chemical action where the steel surface oxidizes, forming iron oxide rust. Many of the systems and components in the plant are made from iron.

Some standard methods associated with material selection that protect against general corrosion include:. Galvanic corrosion occurs when two dissimilar metals with different potentials are placed in electrical contact in an electrolyte. It may also take place with one metal with heterogeneities dissimilarities for example, impurity inclusions, grains of different sizes, difference in composition of grains, or differences in mechanical stress.

A difference in electrical potential exists between the different metals and serves as the driving force for electrical current flow through the corrodant or electrolyte. This current results in corrosion of one of the metals. The larger the potential difference, the greater the probability of galvanic corrosion.

Galvanic corrosion only causes deterioration of one of the metals. The less resistant, more active one becomes the anodic negative corrosion site. The stronger, more noble one is cathodic positive and protected. If there were no electrical contact, the two metals would be uniformly attacked by the corrosive medium. This would then be called general corrosion. For any particular medium, a list can be made arranging metals sequentially from most active, or least noble, to passive, or most noble.

The galvanic series for sea water is discussed in the Chemistry Fundamentals Handbook. Galvanic corrosion is of particular concern in design and material selection. Material selection is important because different metals come into contact with each other and may form galvanic cells. Design is important to minimize differing flow conditions and resultant areas of corrosion buildup. Loose corrosion products are important because they can be transported to the reactor core and irradiated.

In some instances, galvanic corrosion can be helpful in the plant. For example, if pieces of zinc are attached to the bottom of a steel water tank, the zinc will become the anode, and it will corrode. The steel in the tank becomes the cathode, and it will not be effected by the corrosion. This technique is known as cathodic protection. The metal to be protected is forced to become a cathode, and it will corrode at a much slower rate than the other metal, which is used as a sacrificial anode.

Localized corrosion is defined as the selective removal of metal by corrosion at small areas or zones on a metal surface in contact with a corrosive environment, usually a liquid. It usually takes place when small local sites are attacked at a much higher rate than the rest of the original surface. Localized corrosion takes place when corrosion works with other destructive processes such as stress, fatigue, erosion, and other forms of chemical attack.

Localized corrosion mechanisms can cause more damage than any one of those destructive processes individually. There are many different types of localized corrosion.

Pitting, stress corrosion cracking, chloride stress corrosion, caustic stress corrosion, primary side stress corrosion, heat exchanger tube denting, wastage, and intergranular attack corrosion are discussed in detail in the Chemistry Fundamentals Handbook.

One of the most serious metallurgical problems and one that is a major concern in the nuclear industry is stress-corrosion cracking SCC. SCC is a type of intergranular attack corrosion that occurs at the grain boundaries under tensile stress.

It tends to propagate as stress opens cracks that are subject to corrosion, which are then corroded further, weakening the metal by further cracking. The cracks can follow intergranular or transgranular paths, and there is often a tendency for crack branching. The cracks form and propagate approximately at right angles to the direction of the tensile stresses at stress levels much lower than those required to fracture the material in the absence of the corrosive environment.

As cracking penetrates further into the material, it eventually reduces the supporting cross section of the material to the point of structural failure from overload. Stresses that cause cracking arise from residual cold work, welding, grinding, thermal treatment, or may be externally applied during service and, to be effective, must be tensile as opposed to compressive. SCC occurs in metals exposed to an environment where, if the stress was not present or was at much lower levels, there would be no damage.

If the structure, subject to the same stresses, were in a different environment noncorrosive for that material , there would be no failure. Examples of SCC in the nuclear industry are cracks in stainless steel piping systems and stainless steel valve stems. The most effective means of preventing SCC in reactor systems are: 1 designing properly; 2 reducing stress; 3 removing critical environmental species such as hydroxides, chlorides, and oxygen; 4 and avoiding stagnant areas and crevices in heat exchangers where chloride and hydroxide might become concentrated.

Low alloy steels are less susceptible than high alloy steels, but they are subject to SCC in water containing chloride ions. Nickel-based alloys, however, are not effected by chloride or hydroxide ions. An example of a nickel-based alloy that is resistant to stress-corrosion cracking is inconel. One of the most important forms of stress corrosion that concerns the nuclear industry is chloride stress corrosion.

Chloride stress corrosion is a type of intergranular corrosion and occurs in austenitic stainless steel under tensile stress in the presence of oxygen, chloride ions, and high temperature.

It is thought to start with chromium carbide deposits along grain boundaries that leave the metal open to corrosion. This form of corrosion is controlled by maintaining low chloride ion and oxygen content in the environment and use of low carbon steels.

Despite the extensive qualification of inconel for specific applications, a number of corrosion problems have arisen with inconel tubing. Other problems that have been observed with inconel include wastage, tube denting, pitting, and intergranular attack. Personnel need to be aware of the conditions for hydrogen embrittlement and its formation process when selecting materials for a reactor plant. This chapter discusses the sources of hydrogen and the characteristics for the formation of hydrogen embrittlement.

Another form of stress-corrosion cracking is hydrogen embrittlement. Although embrittlement of materials takes many forms, hydrogen embrittlement in high strength steels has the most devastating effect because of the catastrophic nature of the fractures when they occur. Hydrogen embrittlement is the process by which steel loses its ductility and strength due to tiny cracks that result from the internal pressure of hydrogen H 2 or methane gas CH 4 , which forms at the grain boundaries.

In zirconium alloys, hydrogen embrittlement is caused by zirconium hydriding. At nuclear reactor facilities, the term "hydrogen embrittlement" generally refers to the embrittlement of zirconium alloys caused by zirconium hydriding.

Sources of hydrogen causing embrittlement have been encountered in the making of steel, in processing parts, in welding, in storage or containment of hydrogen gas, and related to hydrogen as a contaminant in the environment that is often a by-product of general corrosion. It is the latter that concerns the nuclear industry. Hydrogen may be produced by corrosion reactions such as rusting, cathodic protection, and electroplating. Hydrogen may also be added to reactor coolant to remove oxygen from reactor coolant systems.

As shown in Figure 10, hydrogen diffuses along the grain boundaries and combines with the carbon C , which is alloyed with the iron, to form methane gas. The methane gas is not mobile and collects in small voids along the grain boundaries where it builds up enormous pressures that initiate cracks.

Hydrogen embrittlement is a primary reason that the reactor coolant is maintained at a neutral or basic pH in plants without aluminum components.

If the metal is under a high tensile stress, brittle failure can occur. At normal room temperatures, the hydrogen atoms are absorbed into the metal lattice and diffused through the grains, tending to gather at inclusions or other lattice defects. If stress induces cracking under these conditions, the path is transgranular.

At high temperatures, the absorbed hydrogen tends to gather in the grain boundaries and stress-induced cracking is then intergranular. The cracking of martensitic and precipitation hardened steel alloys is believed to be a form of hydrogen stress corrosion cracking that results from the entry into the metal of a portion of the atomic hydrogen that is produced in the following corrosion reaction.

Hydrogen embrittlement is not a permanent condition. If cracking does not occur and the environmental conditions are changed so that no hydrogen is generated on the surface of the metal, the hydrogen can rediffuse from the steel, so that ductility is restored. To address the problem of hydrogen embrittlement, emphasis is placed on controlling the amount of residual hydrogen in steel, controlling the amount of hydrogen pickup in processing, developing alloys with improved resistance to hydrogen embrittlement, developing low or no embrittlement plating or coating processes, and restricting the amount of in-situ in position hydrogen introduced during the service life of a part.

Hydrogen embrittlement is a problem with zirconium and zirconium alloys, which often are used as cladding materials for nuclear reactors. Zirconium reacts with water as follows. Part of the hydrogen produced by the corrosion of zirconium in water combines with the zirconium to form a separate phase of zirconium hydride ZrH 1. The metal then becomes embrittled ductility decreases and it fractures easily. Cracks begin to form in the zirconium hydride platelets and are propagated through the metal.

Studies at Westinghouse, Batelle, and elsewhere have revealed that the nickel in the zircaloy-2 was responsible for the hydrogen pickup.

This has led to the development of zircaloy- 4, which has significantly less nickel than zircaloy-2 and is less susceptible to embrittlement. In addition, the introduction of niobium into zircaloy-4 further reduces the amount of hydrogen absorption. PDH Classroom offers a continuing education course based on this properties of metals reference page. Engineering Library.

Pumps Valves. Structural Calculators. PDH Classroom. Materials Research Society. The Minerals, Metals and Materials Society. American Society for Engineering Education. Technology Student Association. National Council of Examiners for Engineering and Surveying. National Society of Professional Engineers. ASM International.

Engineering Education Service Center. Materials Engineers. Bureau of Labor Statistics, U. Last Modified Date: Wednesday, January 5, The What They Do tab describes the typical duties and responsibilities of workers in the occupation, including what tools and equipment they use and how closely they are supervised.

This tab also covers different types of occupational specialties. The Work Environment tab includes the number of jobs held in the occupation and describes the workplace, the level of physical activity expected, and typical hours worked. It may also discuss the major industries that employed the occupation. This tab may also describe opportunities for part-time work, the amount and type of travel required, any safety equipment that is used, and the risk of injury that workers may face.

The How to Become One tab describes how to prepare for a job in the occupation. This tab can include information on education, training, work experience, licensing and certification, and important qualities that are required or helpful for entering or working in the occupation.

The Pay tab describes typical earnings and how workers in the occupation are compensated—annual salaries, hourly wages, commissions, tips, or bonuses. Within every occupation, earnings vary by experience, responsibility, performance, tenure, and geographic area.

For most profiles, this tab has a table with wages in the major industries employing the occupation. The Job Outlook tab describes the factors that affect employment growth or decline in the occupation, and in some instances, describes the relationship between the number of job seekers and the number of job openings. The Similar Occupations tab describes occupations that share similar duties, skills, interests, education, or training with the occupation covered in the profile.

The More Information tab provides the Internet addresses of associations, government agencies, unions, and other organizations that can provide additional information on the occupation. The wage at which half of the workers in the occupation earned more than that amount and half earned less. Additional training needed postemployment to attain competency in the skills needed in this occupation.

Work experience that is commonly considered necessary by employers, or is a commonly accepted substitute for more formal types of training or education. The employment, or size, of this occupation in , which is the base year of the employment projections. The projected percent change in employment from to The average growth rate for all occupations is 8 percent. Menu Search button Search:.

Summary Please enable javascript to play this video. What Materials Engineers Do About this section Materials engineers work with metals, ceramics, and plastics to create new materials. Work Environment About this section Materials engineers may work in laboratories or industrial settings to observe the results of their research and development.

How to Become a Materials Engineer About this section Materials engineers plan and evaluate new projects, consulting with others as necessary. Job Outlook About this section Materials Engineers Percent change in employment, projected Total, all occupations. CareerOneStop CareerOneStop includes hundreds of occupational profiles with data available by state and metro area.

Similar Occupations About this section This table shows a list of occupations with job duties that are similar to those of materials engineers. Suggested citation: Bureau of Labor Statistics, U.

What They Do The What They Do tab describes the typical duties and responsibilities of workers in the occupation, including what tools and equipment they use and how closely they are supervised. Work Environment The Work Environment tab includes the number of jobs held in the occupation and describes the workplace, the level of physical activity expected, and typical hours worked. Pay The Pay tab describes typical earnings and how workers in the occupation are compensated—annual salaries, hourly wages, commissions, tips, or bonuses.

Job Outlook The Job Outlook tab describes the factors that affect employment growth or decline in the occupation, and in some instances, describes the relationship between the number of job seekers and the number of job openings. Similar Occupations The Similar Occupations tab describes occupations that share similar duties, skills, interests, education, or training with the occupation covered in the profile.

Contacts for More Information The More Information tab provides the Internet addresses of associations, government agencies, unions, and other organizations that can provide additional information on the occupation.

On-the-job Training Additional training needed postemployment to attain competency in the skills needed in this occupation. Entry-level Education Typical level of education that most workers need to enter this occupation. Work experience in a related occupation Work experience that is commonly considered necessary by employers, or is a commonly accepted substitute for more formal types of training or education.

Number of Jobs, The employment, or size, of this occupation in , which is the base year of the employment projections. Job Outlook, The projected percent change in employment from to Employment Change, The projected numeric change in employment from to Employment Change, projected The projected numeric change in employment from to