Glossary of Terms

Total Page:16

File Type:pdf, Size:1020Kb

Glossary of Terms ASM Handbook, Volume 9: Metallography and Microstructures Copyright © 2004 ASM International® G.F. Vander Voort, editor All rights reserved. www.asminternational.org Glossary of Terms 1-butanol. See n-butyl alcohol. chromatic aberration for two colors. See also alloy system. A complete series of compositions 2-butoxyethanol. See butyl cellosolve. achromatic objective. produced by mixing in all proportions any achromatic objective. Objective are achromatic group of two or more components, at least one when corrected chromatically for two colors, of which is a metal. A generally red and green, and spherically for alpha (␣) The low-temperature allotrope of ti- light of one color, usually in the yellow-green tanium with a hexagonal close-packed crystal aberration. Any error that causes image degra- portion of the spectrum. structure that occurs below the b transus. dation. Such an error may be chromatic, acicular alpha. A product of nucleation and alpha-beta structure. A microstructure contain- spherical, astigmatic, or comatic and can re- growth from b to the lower-temperature allo- ing ␣ and b as the principal phases at a specific sult from design, execution, or both. See also trope ␣ phase. It may have a needlelike ap- temperature. See also beta. astigmatism, chromatic aberration, coma, and pearance in a photomicrograph and may have alpha brass. A solid-solution phase of one or spherical aberration. needle, lenticular, or flattened bar morphology more alloying elements in copper having the abrasion. The process of grinding or wearing in three dimensions. See also alpha. same crystal lattice as copper. away through the use of abrasives; a rough- acid extraction. Removal of phases by disso- alpha case. The oxygen-, nitrogen-, or carbon- ening or scratching of a surface due to abra- lution of the matrix metal in an acid. See also enriched ␣-stabilized surface resulting from sive wear. extraction. elevated-temperature exposure. See also al- abrasion artifact. A false structure introduced adhesive wear. The removal of material from a pha stabilizer. during an abrasion stage of a surface-prepa- surface by the welding together and subse- alpha double prime (orthorhombic marten- ration sequence. quent shearing of a minute area of two sur- site). A supersaturated, nonequilibrium ortho- abrasion fluid. A liquid added to an abrasion faces that slide across each other under pres- rhombic phase formed by a diffusionless system. The liquid may act as a lubricant, as sure. Contrast with abrasive wear. transformation of the b phase in certain alloys. a coolant, or as a means of flushing abrasion age hardening. Hardening by aging, usually af- alpha iron. Solid phase of pure iron that is stable debris from the abrasion track. ter rapid cooling or cold working. See also below 910 ЊC (1670 ЊF), possesses the body- abrasion process. An abrasive machining pro- aging. centered cubic lattice, and is ferromagnetic cedure in which the surface of the workpiece aging. A change in properties that occurs at am- below 768 ЊC (1415 ЊF). is rubbed against a two-dimensional array of bient or moderately elevated temperatures af- alpha prime (hexagonal martensite). A super- abrasive particles under approximately con- ter hot working, heat treating, or cold working saturated, nonequilibrium hexagonal ␣ phase stant load. (strain aging). The change in properties is of- formed by a diffusionless transformation of abrasion rate. The rate at which material is re- ten due to a phase change (precipitation) but the b phase. It is often difficult to distinguish moved from a surface during abrasion. It is does not alter chemical composition. See also from acicular ␣, although the latter is usually usually expressed in terms of the thickness re- age hardening, artificial aging, interrupted less well defined and frequently has curved, moved per unit of time or distance traversed. aging, natural aging, overaging, precipitation instead of straight, sides. abrasive. A substance capable of removing ma- hardening, precipitation heat treatment, pro- alpha stabilizer. An alloying element that dis- terial from another substance in machining, gressive aging, quench aging, step aging, and solves preferentially in the ␣ phase and raises abrasion, or polishing that usually takes the strain aging. the ␣-b transformation temperature. form of several small, irregularly shaped par- alignment. A mechanical or electrical adjust- alpha transus. The temperature that designates ticles of a hard material. ment of the components of an optical device b ם ␣ the phase boundary between the ␣ and abrasive machining. A machining process in so that the path of the radiating beam coin- fields. which the points of abrasive particles are used cides with the optical axis or other predeter- aluminum chloride, anhydrous. as machining tools. Grinding is a typical abra- mined path in the system. See also magnetic Solid; AlCl3; sive machining process. reacts violently with water, evolving HCl gas; alignment, mechanical alignment, and voltage • abrasive wear. The removal of material from a alignment. use of hydrated form, AlCl3 6H2O, is pre- surface when hard particles slide or roll across allotriomorphic crystal. A crystal having a nor- ferred. the surface under pressure. The particles may mal lattice structure but an outward shape that ammonium molybdate. Crystals; also called be loose or may be part of another surface in is imperfect, because it is determined to some ammonium paramolybdate or heptamolyb- • contact with the surface being abraded. Con- extent by the surroundings. The grains in a date; (NH4)6Mo7O42 4H2O; can be used inter- trast with adhesive wear. metallic aggregate are allotriomorphic crys- changeably with “molybdic acid, 85%.” a-butyl alcohol. Liquid; normal butyl alcohol; tals. Compare with idiomorphic crystal. amplifier. A negative lens used instead of an also called butyl alcohol and 1-butanol. allotropy. The property by which certain ele- eyepiece to project under magnification the accelerating potential. A relatively high voltage ments may exist in more than one crystal image formed by an objective. The amplifier applied between the cathode and anode of an structure. See also polymorphism. is designed for flatness of field and should be electron gun to accelerate electrons. alloying element. An element added to and re- used with an apochromatic objective. achromatic. Free of color. A lens or objective is maining in a metal that changes structure and analyzer. An optical device capable of produc- achromatic when corrected for longitudinal properties. ing plane-polarized light. It is used for detect- 1116 / Reference Information ing the effect of the object on plane-polarized aperture (optical). In optical microscopy, the axis (crystal). The edge of the unit cell of a light produced by the polarizer. working diameter of a lens or a mirror. See space lattice. Any one axis of any one lattice angle of reflection. (1) Reflection: the angle be- also angular aperture. is defined in length and direction relative to tween the reflected beam and the normal to aplanatic. Corrected for spherical aberration and other axes of that lattice. the reflecting surfaces. See also normal. (2) coma. Diffraction: the angle between the diffracted apochromatic objective. Objectives corrected beam and the diffracting planes. chromatically for three colors and spherically angstrom unit (A˚ ). A unit of linear measure for two colors are called apochromats. These B -m, or 0.1 nm. Although not an corrections are superior to those of the ach 10מequal to 10 accepted SI unit, it is occasionally used for romatic series of lenses. Because apochromats backing film. A film used as auxiliary support small distances, such as interatomic distances, are not well corrected for lateral color, special for the thin replica or specimen-supporting and some wavelengths. eyepieces are used to compensate. See also film. angular aperture. In optical microscopy, the an- achromatic. back reflection. The diffraction of x-rays at a gle between the most divergent rays that can artifact. A feature of artificial character, such as Bragg angle approaching 90Њ. pass through a lens to form the image of an a scratch or a piece of dust on a metallographic bainite. A eutectoid transformation product of object. See also aperture (optical). specimen, that can be erroneously interpreted ferrite and a fine dispersion of carbide gener- anisotropy. Characterized by having different as a real feature. See also abrasion artifact, ally formed below 450 to 500 ЊC (840 to 930 values of a property in different directions. mounting artifact, and polishing artifact. ЊF). Upper bainite is an aggregate that con- annealing. A generic term denoting a treat- artificial aging. Aging above room temperature. tains parallel lath-shaped units of ferrite, pro- ment—heating to and holding at a suitable Compare with natural aging. duces the so-called “feathery” appearance in temperature, followed by cooling at a suitable astigmatism. A defect in a lens or optical system optical microscopy, and is formed above ap- Њ Њ rate—used primarily to soften metallic mate- that causes rays in one plane parallel to the proximately 350 C (660 F). Lower bainite, rials but also to produce desired changes si- optical axis to focus at a distance different which has an acicular appearance similar to multaneously in other properties or in micro- from those in the plane at right angles to it. tempered martensite, is formed below approx- Њ Њ structure. When applied only for the relief of ASTM grain size number. See grain size. imately 350 C (660 F). stress, the process is called stress relieving or athermal. Not isothermal. Changing rather than banding. Inhomogeneous distribution of alloy- stress-relief annealing. In ferrous alloys, an- constant temperature conditions. ing elements or phases aligned in filaments or nealing is carried out above the upper critical atomic replica. A thin replica devoid of struc- plates parallel to the direction of working. See temperature, but the time-temperature cycles ture on the molecular level. It is prepared by also ferrite-pearlite banding and segregation vary widely in maximum temperature attained the vacuum or hydrolytic deposition of metals banding.
Recommended publications
  • Crystal Structures
    Crystal Structures Academic Resource Center Crystallinity: Repeating or periodic array over large atomic distances. 3-D pattern in which each atom is bonded to its nearest neighbors Crystal structure: the manner in which atoms, ions, or molecules are spatially arranged. Unit cell: small repeating entity of the atomic structure. The basic building block of the crystal structure. It defines the entire crystal structure with the atom positions within. Lattice: 3D array of points coinciding with atom positions (center of spheres) Metallic Crystal Structures FCC (face centered cubic): Atoms are arranged at the corners and center of each cube face of the cell. FCC continued Close packed Plane: On each face of the cube Atoms are assumed to touch along face diagonals. 4 atoms in one unit cell. a 2R 2 BCC: Body Centered Cubic • Atoms are arranged at the corners of the cube with another atom at the cube center. BCC continued • Close Packed Plane cuts the unit cube in half diagonally • 2 atoms in one unit cell 4R a 3 Hexagonal Close Packed (HCP) • Cell of an HCP lattice is visualized as a top and bottom plane of 7 atoms, forming a regular hexagon around a central atom. In between these planes is a half- hexagon of 3 atoms. • There are two lattice parameters in HCP, a and c, representing the basal and height parameters Volume respectively. 6 atoms per unit cell Coordination number – the number of nearest neighbor atoms or ions surrounding an atom or ion. For FCC and HCP systems, the coordination number is 12. For BCC it’s 8.
    [Show full text]
  • Extrusion.Pdf
    Extrusion: Second Edition Copyright © 2006 ASM International® M. Bauser, G. Sauer, K. Siegert, editors, p 195-321 All rights reserved. DOI:10.1361/exse2006p195 www.asminternational.org CHAPTER 5 The Production of Extruded Semifinished Products from Metallic Materials* THE HOT-WORKING PROCESS extrusion ered to be the most important of the hot-working is, in contrast to other compressive deformation processes. processes used to produce semifinished prod- ucts, a deformation process with pure compres- sive forces in all three force directions. These favorable deformation conditions do not exist in other production processes for semifinished products. Even in rolling, which is the most im- Extrusion of Materials with portant compressive working process for pro- ducing semifinished products, tensile forces oc- Working Temperatures cur in the acceleration zone of the roll gap as between 0 and 300 ЊC well as in the cross rolling process used to pierce blanks in the rolling of steel tubes. These Gu¨nther Sauer* tensile forces cause problems in the rolled prod- uct if the deformation conditions are not opti- mized. The benefits of this three-dimensional compression in terms of deformation technol- 5.1 Extrusion of Semifinished ogy, which have already been discussed in this Products in Tin Alloys book, can be clearly seen in Fig. 5.1 based on experimental results for face-centred cubic (fcc) Tin is a silver-white, very soft metal with a aluminum and zinc with its hexagonal lattice stable tetragonal lattice in the temperature range structure. 20 to 161 ЊC. The pure metal has a density of The extensive variations in the extrusion pro- 7.28 g/cm3 and a melting point of 232 ЊC.
    [Show full text]
  • Synthesis and Characterisation of Carbide Derived Carbons
    Synthesis and Characterisation of Carbide Derived Carbons Sigita Urbonaite Department of Physical, Inorganic and Structural Chemistry Stockholm University 2008 Doctoral Thesis 2008 Department of Physical, Inorganic and Structural Chemistry Stockholm University Cover: Some artefacts found during TEM investigation of CDCs. Faculty opponent: Prof. Rik Brydson Department of Nanoscale Materials Characterisation Institute for Materials Research University of Leeds, UK Evaluation committee: Prof. Bertil Sundqvist, Nanofysik och material, UmU Prof. Margareta Sundberg, Strukturkemi, SU Prof. Kristina Edström, Strukturkemi, UU Docent Lioubov Belova, Teknisk materialfysik, KTH © Sigita Urbonaite, Stockholm 2008 ISBN 978-91-7155-589-2 pp. 1-82. Printed in Sweden by US-AB, Stockholm 2008 Distributor: FOOS/Structurkemi ii ABSTRACT Carbide derived carbons (CDCs) have been synthesised through chlorina- tion of VC, TiC, WC, TaC, NbC, HfC and ZrC at different temperatures. The aim of the investigation was to systematically study changes of struc- tural and adsorption properties depending on the synthesis conditions. CDCs were characterised using nitrogen and carbon dioxide adsorption, Raman spectroscopy, scanning electron microscopy, transmission electron micros- copy, and electron energy loss spectroscopy. The studies revealed the CDCs structures to range from amorphous to ordered, from microporous to mesoporous. It was found that structural ordering and porosity can be modi- fied by: i) synthesis temperature, ii) precursor, iii) density and volume of precursor, iv) catalysts, v) incorporation of nitrogen in to carbide structure, and CDCs can be tuned up to the demanded quality. They also exhibited a high potential for methane storage. iii iv LIST OF PUBLICATIONS Paper I. Porosity development along the synthesis of carbons from metal carbides S.
    [Show full text]
  • Carbon – Science and Technology
    © Applied Science Innovations Pvt. Ltd., India Carbon – Sci. Tech. 1 (2010) 139 - 143 Carbon – Science and Technology ASI ISSN 0974 – 0546 http://www.applied-science-innovations.com ARTICLE Received :29/03/2010, Accepted :02/09/2010 ----------------------------------------------------------------------------------------------------------------------------- Ablation morphologies of different types of carbon in carbon/carbon composites Jian Yin, Hongbo Zhang, Xiang Xiong, Jinlv Zuo State Key Laboratory of Powder Metallurgy, Central South University, Lushan South Road, Changsha, China. --------------------------------------------------------------------------------------------------------------------------------------- 1. Introduction : Carbon/carbon (C/C) composites the ablation morphology and formation mechanism of combine good mechanical properties and designable each types of carbon. capabilities of composites and excellent ultrahigh temperature properties of carbon materials. They have In this study, ablation morphologies of resin-based low densities, high specific strength, good thermal carbon, carbon fibers, pyrolytic carbon with smooth stability, high thermal conductivity, low thermal laminar structure and rough laminar structure has been expansion coefficient and excellent ablation properties investigated in detail and their formation mechanisms [1]. As C/C composites show excellent characteristics were discussed. in both structural design and functional application, 2 Experimental : they have become one of the most competitive high temperature materials widely used in aviation and 2.1 Preparation of C/C composites : Bulk needled polyacrylonitrile (PAN) carbon fiber felts spacecraft industry [2 - 4]. In particular, they are were used as reinforcements. Three kinds of C/C considered to be the most suitable materials for solid composites, labeled as sample A, B and C, were rocket motor nozzles. prepared. Sample A is a C/C composite mainly with C/C composites are composed of carbon fibers and smooth laminar pyrolytic carbon, sample B is a C/C carbon matrices.
    [Show full text]
  • Quartz Crystal Division of Seiko Instruments Inc
    (1) Quartz Crystal Division of Seiko Instruments Inc. and affiliates, which is responsible for manufacturing the products described in this catalogue, holds ISO 9001 and ISO 14001 certification. (2) SII Crystal Technology Inc. Tochigi site holds IATF 16949 certification. Quartz Crystal Product Catalogue Electronic Components Sales Head Office 1-8, Nakase, Mihamaku, Chiba-shi, Chiba 261-8507, Japan Telephone:+81-43-211-1207 Facsimile:+81-43-211-8030 E-mail:[email protected] <Manufacturer> SII Crystal Technology Inc. 1110, Hirai-cho, Tochigi-shi, Tochigi 328-0054, Japan Released in February 2019 No.QTC2019EJ-02C1604 Creating Time - Optimizing Time - Enriching Time Seiko Instruments Inc. (SII), founded in 1937 as a member of the Seiko Group specializing in the manufacture of watches, has leveraged its core competency in high precision watches to create a wide range of new products and technologies. Over the years SII has developed high-precision processed parts and machine tools that pride themselves on their sub-micron processing capability, quartz crystals that came about as a result of our quartz watch R&D, and electronic components such as micro batteries. Optimizing our extensive experience and expertise, we have since diversified into such new fields as compact, lightweight, exceedingly quiet thermal printers, and inkjet printheads, a key component in wide format inkjet printers for corporate use. SII, in the years to come, will maintain an uncompromised dedication to its time-honored technologies and innovations of craftsmanship, miniaturization, and efficiency that meet the needs of our changing society and enrich the lives of those around us. SEIKO HOLDINGS GROUP 1881 1917 1983 1997 2007 K.
    [Show full text]
  • WHAT IS...A Quasicrystal?, Volume 53, Number 8
    ?WHAT IS... a Quasicrystal? Marjorie Senechal The long answer is: no one is sure. But the short an- diagrams? The set of vertices of a Penrose tiling does— swer is straightforward: a quasicrystal is a crystal that was known before Shechtman’s discovery. But with forbidden symmetry. Forbidden, that is, by “The what other objects do, and how can we tell? The ques- Crystallographic Restriction”, a theorem that confines tion was wide open at that time, and I thought it un- the rotational symmetries of translation lattices in two- wise to replace one inadequate definition (the lattice) and three-dimensional Euclidean space to orders 2, 3, with another. That the commission still retains this 4, and 6. This bedrock of theoretical solid-state sci- definition today suggests the difficulty of the ques- ence—the impossibility of five-fold symmetry in crys- tion we deliberately but implicitly posed. By now a tals can be traced, in the mineralogical literature, back great many kinds of aperiodic crystals have been to 1801—crumbled in 1984 when Dany Shechtman, a grown in laboratories around the world; most of them materials scientist working at what is now the National are metals, alloys of two or three kinds of atoms—bi- Institute of Standards and Technology, synthesized nary or ternary metallic phases. None of their struc- aluminium-manganese crystals with icosahedral sym- tures has been “solved”. (For a survey of current re- metry. The term “quasicrystal”, hastily coined to label search on real aperiodic crystals see, for example, the such theretofore unthinkable objects, suggests the website of the international conference ICQ9, confusions that Shechtman’s discovery sowed.
    [Show full text]
  • Crystal Structure of a Material Is Way in Which Atoms, Ions, Molecules Are Spatially Arranged in 3-D Space
    Crystalline Structures – The Basics •Crystal structure of a material is way in which atoms, ions, molecules are spatially arranged in 3-D space. •Crystal structure = lattice (unit cell geometry) + basis (atom, ion, or molecule positions placed on lattice points within the unit cell). •A lattice is used in context when describing crystalline structures, means a 3-D array of points in space. Every lattice point must have identical surroundings. •Unit cell: smallest repetitive volume •Each crystal structure is built by stacking which contains the complete lattice unit cells and placing objects (motifs, pattern of a crystal. A unit cell is chosen basis) on the lattice points: to represent the highest level of geometric symmetry of the crystal structure. It’s the basic structural unit or building block of crystal structure. 7 crystal systems in 3-D 14 crystal lattices in 3-D a, b, and c are the lattice constants 1 a, b, g are the interaxial angles Metallic Crystal Structures (the simplest) •Recall, that a) coulombic attraction between delocalized valence electrons and positively charged cores is isotropic (non-directional), b) typically, only one element is present, so all atomic radii are the same, c) nearest neighbor distances tend to be small, and d) electron cloud shields cores from each other. •For these reasons, metallic bonding leads to close packed, dense crystal structures that maximize space filling and coordination number (number of nearest neighbors). •Most elemental metals crystallize in the FCC (face-centered cubic), BCC (body-centered cubic, or HCP (hexagonal close packed) structures: Room temperature crystal structure Crystal structure just before it melts 2 Recall: Simple Cubic (SC) Structure • Rare due to low packing density (only a-Po has this structure) • Close-packed directions are cube edges.
    [Show full text]
  • Determination of Focal Length of a Converging Lens and Mirror
    Physics 41- Lab 5 Determination of Focal Length of A Converging Lens and Mirror Objective: Apply the thin-lens equation and the mirror equation to determine the focal length of a converging (biconvex) lens and mirror. Apparatus: Biconvex glass lens, spherical concave mirror, meter ruler, optical bench, lens holder, self-illuminated object (generally a vertical arrow), screen. Background In class you have studied the physics of thin lenses and spherical mirrors. In today's lab, we will analyze several physical configurations using both biconvex lenses and concave mirrors. The components of the experiment, that is, the optics device (lens or mirror), object and image screen, will be placed on a meter stick and may be repositioned easily. The meter stick is used to determine the position of each component. For our object, we will make use of a light source with some distinguishing marking, such as an arrow or visible filament. Light from the object passes through the lens and the resulting image is focused onto a white screen. One characteristic feature of all thin lenses and concave mirrors is the focal length, f, and is defined as the image distance of an object that is positioned infinitely far way. The focal lengths of a biconvex lens and a concave mirror are shown in Figures 1 and 2, respectively. Notice the incoming light rays from the object are parallel, indicating the object is very far away. The point, C, in Figure 2 marks the center of curvature of the mirror. The distance from C to any point on the mirror is known as the radius of curvature, R.
    [Show full text]
  • Identifying the Elastic Isotropy of Architectured Materials Based On
    Identifying the elastic isotropy of architectured materials based on deep learning method Anran Wei a, Jie Xiong b, Weidong Yang c, Fenglin Guo a, d, * a Department of Engineering Mechanics, School of Naval Architecture, Ocean and Civil Engineering, Shanghai Jiao Tong University, Shanghai 200240, China b Department of Mechanical Engineering, The Hong Kong Polytechnic University, Kowloon, Hong Kong, China c School of Aerospace Engineering and Applied Mechanics, Tongji University, Shanghai 200092, China d State Key Laboratory of Ocean Engineering, Shanghai Jiao Tong University, Shanghai 200240, China * Corresponding author, E-mail: [email protected] Abstract: With the achievement on the additive manufacturing, the mechanical properties of architectured materials can be precisely designed by tailoring microstructures. As one of the primary design objectives, the elastic isotropy is of great significance for many engineering applications. However, the prevailing experimental and numerical methods are normally too costly and time-consuming to determine the elastic isotropy of architectured materials with tens of thousands of possible microstructures in design space. The quick mechanical characterization is thus desired for the advanced design of architectured materials. Here, a deep learning-based approach is developed as a portable and efficient tool to identify the elastic isotropy of architectured materials directly from the images of their representative microstructures with arbitrary component distributions. The measure of elastic isotropy for architectured materials is derived firstly in this paper to construct a database with associated images of microstructures. Then a convolutional neural network is trained with the database. It is found that the convolutional neural network shows good performance on the isotropy identification.
    [Show full text]
  • Appendix F. Glossary
    Appendix F. Glossary 2DEG 2-dimensional electron gas A/D Analog to digital AAAR American Association for Aerosol Research ADC Analog-digital converter AEM Analytical electron microscopy AFM Atomic force microscope/microscopy AFOSR Air Force Office of Scientific Research AIST (Japan) Agency of Industrial Science and Technology AIST (Japan, MITI) Agency of Industrial Science and Technology AMLCD Active matrix liquid crystal display AMM Amorphous microporous mixed (oxides) AMO Atomic, molecular, and optical AMR Anisotropic magnetoresistance ARO (U.S.) Army Research Office ARPES Angle-resolved photoelectron spectroscopy ASET (Japan) Association of Super-Advanced Electronics Technologies ASTC Australia Science and Technology Council ATP (Japan) Angstrom Technology Partnership ATP Adenosine triphosphate B Magnetic flux density B/H loop Closed figure showing B (magnetic flux density) compared to H (magnetic field strength) in a magnetizable material—also called hysteresis loop bcc Body-centered cubic BMBF (Germany) Ministry of Education, Science, Research, and Technology (formerly called BMFT) BOD-FF Bond-order-dependent force field BRITE/EURAM Basic Research of Industrial Technologies for Europe, European Research on Advanced Materials program CAD Computer-assisted design CAIBE Chemically assisted ion beam etching CBE Chemical beam epitaxy 327 328 Appendix F. Glossary CBED Convergent beam electron diffraction cermet Ceramic/metal composite CIP Cold isostatic press CMOS Complementary metal-oxide semiconductor CMP Chemical mechanical polishing
    [Show full text]
  • How Does the Light Adjustable Lens Work? What Should I Expect in The
    How does the Light Adjustable Lens work? The unique feature of the Light Adjustable Lens is that the shape and focusing characteristics can be changed after implantation in the eye using an office-based UV light source called a Light Delivery Device or LDD. The Light Adjustable Lens itself has special particles (called macromers), which are distributed throughout the lens. When ultraviolet (UV) light from the LDD is directed to a specific area of the lens, the particles in the path of the light connect with other particles (forming polymers). The remaining unconnected particles then move to the exposed area. This movement causes a highly predictable change in the curvature of the lens. The new shape of the lens will match the prescription you selected during your eye exam. What should I expect in the period after cataract surgery? Please follow all instructions provided to you by your eye doctor and staff, including wearing of the UV-blocking glasses that will be provided to you. As with any cataract surgery, your vision may not be perfect after surgery. While your eye doctor selected the lens he or she anticipated would give you the best possible vision, it was only an estimate. Fortunately, you have selected the Light Adjustable Lens! In the next weeks, you and your eye doctor will work together to optimize your vision. Please make sure to pay close attention to your vision and be prepared to discuss preferences with your eye doctor. Why do I have to wear UV-blocking glasses? The UV-blocking glasses you are provided with protect the Light Adjustable Lens from UV light sources other than the LDD that your doctor will use to optimize your vision.
    [Show full text]
  • ROLLING of METAL (Auxiliary Operations Used in Connection With
    CPC - B21B - 2017.08 B21B ROLLING OF METAL (auxiliary operations used in connection with metal- working operations covered in B21, see B21C; bending by rolling B21D; manufacture of particular objects, e.g. screws, wheels, rings, barrels, balls, by rolling B21H; pressure welding by means of a rolling mill B23K 20/04) Definition statement This place covers: Methods and devices for rolling of metal. Rolling is a metal forming process in which metal is passed through a pair of rotating rolls for plastic deformation of the metall. Rolling is classified according to the temperature of the metal rolled. If the temperature of the metal is above its recrystallization temperature, then the process is termed as hot rolling. If the temperature of the metal is below its recrystallization temperature, the process is termed as cold rolling. A rolling mill is a machine for plastic deformation of metal between rotating rolls. In a broader sense, a rolling mill is an automatic system or line of machines that performs both rolling and auxiliary operations: transport of the original billet from the stock to the heating furnaces and the mill rolls, transfer of the rolled material from one groove to another, turning, transport of the metal after rolling, cutting into sections, marking or stamping, trimming, packing, and conveyance to the stock of finished product. This subclass includes the following main groups: Rolling of metal in general: • Methods or devices in general B21B 1/00, B21B 11/00 - B21B 13/00 • Control B21B 37/00 • Measuring B21B 38/00 • Operation B21B 35/00, B21B 39/00, B21B 41/00 • Details of rolling mills B21B 27/00, B21B 29/00, B21B 31/00 • Maintenance of rolling rolls B21B 28/00 • Safety devices B21B 33/00 • Cooling beds and accessories B21B 43/00 Rolling of special formats: • tube rolling B21B 17/00, B21B 19/00, B21B 23/00 1 B21B (continued) CPC - B21B - 2017.08 • accessories for tube rolling B21B 25/00 • Extending closed shapes of metal bands B21B 5/00 Rolling of special alloys: B21B 3/00 Rolling of metal under special conditions (e.g.
    [Show full text]