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Relevant bibliographies by topics / Surface

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Academic literature on the topic 'Surface'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 April 2025

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Journal articles on the topic "Surface"

1

Chan, Chi-Ming, Lu-Tao Wang, and Lin Li. "Applications of Surface Analysis Techniques in Surface Characterization of Polymer Surfaces and Interfaces." Journal of The Adhesion Society of Japan 38, no. 5 (2002): 173–92. http://dx.doi.org/10.11618/adhesion.38.173.

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CHUMA, Kenichiro, Yuji FURUKAWA, Yujie HAN, and Akira KAKUTA. "A Study on Surface Integrity of SiC/Si Hybrid Nano-Structured Surfaces(Surface and edge finishing)." Proceedings of International Conference on Leading Edge Manufacturing in 21st century : LEM21 2005.3 (2005): 1199–204. http://dx.doi.org/10.1299/jsmelem.2005.3.1199.

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Grigoruk, V. I., V. I. Kanevskii, S. A. Kolenov, and V. S. Sidorenko. "Scattering of light by quartz rough surface described as sequence of surface three-cornered form irregularities." Surface 9(24) (December 30, 2017): 69–80. http://dx.doi.org/10.15407/surface.2017.09.069.

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Cha, Judy J., and Yi Cui. "The surface surfaces." Nature Nanotechnology 7, no. 2 (February 2012): 85–86. http://dx.doi.org/10.1038/nnano.2012.9.

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Kevan, S. D. "Surface Fermi Surfaces." Physica Scripta T31 (January 1, 1990): 32–34. http://dx.doi.org/10.1088/0031-8949/1990/t31/005.

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Vlasova, N. M., and O. V. Markitan. "Adsorption of adenine nucleotides on the nanocrystalline ceria surface." Surface 9(24) (December 30, 2017): 96–103. http://dx.doi.org/10.15407/surface.2017.09.096.

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Semchuk, O. Yu, O. O. Havryliuk, and A. A. Biliuk. "Kinetic theory of surface plasmon resonance in metal nanoparticles." Surface 12(27) (December 30, 2020): 3–19. http://dx.doi.org/10.15407/surface.2020.12.003.

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In recent years, interest in studying the optical properties of metallic nanostructures has grown. This interest is primarily related to the possibility of practical application of such nanostructures in quantum optical computers, micro- and nanosensors. These applications are based on the fundamental optical effect of surface plasmon excitation. The consequence of this phenomenon is surface plasmon resonance (SPR) - an increase in the cross section of energy absorption by a metal nanoparticle as the frequency of incident light (laser radiation) approaches the SPR frequency of the nanoparticle. Plasmon structures are used to improve the efficiency of thin-film SC. In such structures, metal nanoparticles can primarily act as additional scattering elements for the long-wavelength component of sunlight illuminating SC. As a collective phenomenon, SPR can be described using kinetic approaches, ie using the Boltzmann kinetic equation for the conduction electrons of metal nanoparticles. In this work, the theory of SPR based on the kinetic equation for the conduction electrons of nanoparticles is constructed. to the well-known results derived from the Drude-Sommerfeld theory. Second, the kinetic method makes it possible to study metal nanoparticles with sizes larger or ptical conductivity tensor for spheroidal metal nanoparticles. It is shown that the effect of nanoparticle asymmetry on the ratio of the components of the optical conductivity tensor differs not only smaller than the average electron free path length. The developed theory is used to calculate the oquantitatively but also qualitatively in high-frequency and low-frequency surface scattering. It was found that in metal nanoparticles in a dielectric matrix, under SPR conditions, the full width of the SPR line in a spherical metal nanoparticle depends on both the radius of the particle and the frequency of the electromagnetic (laser) radiation exciting this SPR. It is shown that oscillations of the SPR line width with a change in the dielectric constant of the medium in which they are located can be observed in metal nanoparticles. The magnitude of these oscillations is greater the smaller the size of the nanoparticle and increases significantly with increase. As the radius of the spherical nanoparticle increases, the width of the SPR line decreases significantly and prevails around a certain constant value in media with a higher value of dielectric constant.

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Nasiedkin, D. B., M. O. Nazarchuk, A. G. Grebenyuk, L. F. Sharanda, and Yu V. Plyuto. "Quantum chemical simulation of MoO3 dispergation on hydroxylated SiO2 surface." Surface 13(28) (December 30, 2021): 75–83. http://dx.doi.org/10.15407/surface.2021.13.075.

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Метою даної роботи є оцінка енергетичної сприятливості утворення різних молібдатних груп (≡Si‑O‑)2Mo(=O)2 та =Si(‑O‑)2Mo(=O)2 під час термічно ініційованого диспергування MoO3 на гідроксильованій поверхні SiO2. Для цього було здійснено квантовохімічне моделювання реакції O12Si10(OH)16 + MoO3 = O12Si10(OH)14O2MoO2 + H2O в температурному інтервалі 300–1100 K із використанням обмеженого методу Хартрі-Фока (наближення ЛКАО) з валентним базисом SBKJC (Stevens-Basch-Krauss-Jasien-Cundari). Кластер O12Si10(OH)16, який являє собою структурний фрагмент кристала β‑кристобаліту, був використаний як модель високогідроксильованої поверхні кремнезему. Ми розглянули дві структури молібдатних груп (≡Si‑O‑)2Mo(=O)2, прикріплених до кремнеземного кластера O12Si10(OH)16 через силанольні групи. Молібдатні групи (Etot ‑584.60147 Hartree), прикріплені до кремнеземного кластера через віддалені силанольні групи, виявляються більш енергетично вигідними, ніж молібдатні групи (Etot ‑584.56565 Hartree), прикріплені до кремнеземного кластера через сусідні силанольні групи. Енергія молібдатних груп =Si(‑O‑)2Mo(=O)2 (Etot ‑584.48399 Hartree), прикріплених до кремнеземного кластера O12Si10(OH)16 через силандіольні групи, менш енергетично вигідні в порівнянні з подібними групами, прикріпленими через силанольні групи, через більше напруження кута між зв’язками. Знайдено, що реакція O12Si10(OH)16 + MoO3 = O12Si10(OH)14O2MoO2 + H2O в температурному інтервалі 300–1100 K, змодельована шляхом квантовохімічних розрахунків, свідчить, що процес диспергування MoO3 на гідроксильованій поверхні SiO2 є енергетично вигідним. Експ The aim of the present work is to evaluate the energetic favourability of the formation of different molybdate species (≡Si‑O‑)2Mo(=O)2 and =Si(‑O‑)2Mo(=O)2 during the thermally induced MoO3 dispergation on hydroxylated SiO2 surface. In order to do this a quantum chemical modelling of the reaction O12Si10(OH)16 + MoO3 = O12Si10(OH)14O2MoO2 + H2O within the temperature interval of 300–1100 K was undertaken using the Restricted Hartree-Fock method (the LCAO approximation) with the SBKJC (Stevens-Basch-Krauss-Jasien-Cundari) valence basis set. The cluster O12Si10(OH)16 which represents a structural fragment of a β‑cristobalite crystal was used in this work as a model of highly hydroxylated silica surface. We considered two structures of molybdate (≡Si‑O‑)2Mo(=O)2 species attached to O12Si10(OH)16 silica cluster via silanol groups. Molybdate species (Etot ‑584.60147 Hartree) attached to silica cluster via distant silanols appeared more energetically favourable than molybdate species (Etot ‑584.56565 Hartree) attached to silica cluster via nearby silanols. The energy of molybdate =Si(‑O‑)2Mo(=O)2 species (Etot ‑584.48399 Hartree) attached to O12Si10(OH)16 silica cluster via silanediol group is less favourable energetically in comparison with those attached via silanol groups because of higher bond angle straining. The reaction O12Si10(OH)16 + MoO3 = O12Si10(OH)14O2MoO2 + H2O in the temperature interval of 300–1100 K which simulates by quantum chemical calculations the dispergation of MoO3 on hydroxylated SiO2 surface was found to be energetically favourable. The experimentally optimised temperature of ca. 800 K required for dispergation of MoO3 on hydroxylated SiO2 surface is determined by MoO3 evaporation and transportation via the gas phase. ериментальна оптимальна температура (близько 800 K), потрібна для диспергування MoO3 на гідроксильованій поверхні SiO2, визначається випаровуванням та перенесенням MoO3 в газовій фазі.

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Terebinska, M. I., O. I. Tkachuk, and V. V. Lobanov. "X-ray photoelectron spectroscopy and auger in research solid surface." Surface 8(23) (December 30, 2016): 15–49. http://dx.doi.org/10.15407/surface.2016.08.015.

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Plyuto, Yu V., L. F. Sharanda, D. B. Nasedkin, and I. V. Babich. "Characterisation of Mo(VI) oxo-species on the surface of the rationally designed MoO3/Al2O3 and MoO3/SiO2 model systems." Surface 16(31) (December 30, 2024): 164–72. https://doi.org/10.15407/surface.2024.16.164.

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Model well-defined MoO3/Al2O3 and MoO3/SiO2 systems were rationally designed by anchoring of MoOCl4 on the supports surface of fumed Al2O3 and SiO2 nanoparticles. The subsequent hydrolysis of the anchored groups by water vapours followed by thermal treatment resulted in the formation of Mo(VI) oxo-species on the supports surface. By application of the anchoring – hydrolysis cycles the model MoO3/Al2O3 systems with the molybdena loading of 1.10, 1.92 and 2.34 Mo/nm2 were synthesised. The synthesised MoO3/SiO2 systems had a molybdena loading of 0.82, 1.05 and 1.21 Mo/nm2. X-ray diffraction patterns characteristic for MoO3 crystallites were not observed in the synthesised MoO3/Al2O3 and MoO3/SiO2 systems up to the highest achieved molybdena loading of 2.34 and 1.21 Mo/nm2 respectively. This confirms that the used preparation route resulted in the formation of highly dispersed Mo(VI) oxo-species on the surface of both Al2O3 and SiO2 supports. The degree of aggregation of Mo(VI) oxo-species depends on the nature of the support surface and molybdena loading. Increase of the molybdena loading on the surface of both Al2O3 and SiO2 supports results in an increase of the degree of aggregation of Mo(VI) oxo-species. On Al2O3 support, at a molybdena loading which corresponds to the population of surface hydroxyl groups, monomeric Mo(VI) oxo-species appear to be predominant. At higher molybdena loading, the formation of polymeric Mo(VI) oxo-species was detected. On SiO2 support, at a molybdena loading which corresponds or exceeds the population of surface hydroxyl groups, simultaneous presence of monomeric and polymeric Mo(VI) oxo-species was observed.

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Dissertations / Theses on the topic "Surface"

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Chen, Yizhou. "Adhesion of Spider Glue on Different Surface Energy and Surface Potential Surfaces." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1462227997.

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Kruithof, Nico Gerard Hugo. "Envelope surfaces surface design and meshing /." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 2006. http://irs.ub.rug.nl/ppn/292152264.

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Johansson, Lars. "SURFACE DRAG MODELING FOR MILLED SURFACES." Thesis, KTH, Mekanik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-204017.

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One of the governing sources of energy loss in a modern day jet engine is attributed to surfacedrag. This energy loss can be divided into friction loss and to surface geometry loss. Thefriction loss is the shear stress the fluid experience due to a no slip condition at the wall, whilethe surface geometry loss is due to pressure drop when the fuel passes an obstacle.The objective of this work is to study the drag coefficient of a plate for different types ofmilled tracks and for different kinds of flow conditions. The theories used to calculate thedrag coefficient are based on the momentum thickness theory including shear stress- andpressure integration. The computations were carried out with ANSYS CFX assuming a ShearStress Transport 𝑘 − 𝜔 turbulence model. The steady state flow conditions tested are varyingboundary layer thicknesses, milled track heights, milled track widths, Reynolds numbers overthe milled track height, Reynolds numbers over the plate length and free-stream angle ofattack. By knowing what affects the drag coefficient for different types of milled tracks, morepractical models can be developed making the prediction of surface drag inside the jet enginemore accurate.This report has resulted in a formula that predicts the drag coefficient for different types ofmilled surfaces. The formula is derived from the assumption that the CFD results on ANSYSCFX are correct. A physical test has not been made to verify those results, however this has tobe done to prove that this formula is valid.

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Shukla, Nisha. "Surface spectroscopic studies of coadsorbed molecules and surface reactions at single crystal metal surfaces." Thesis, Cardiff University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275212.

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Zheleva, Zhasmina Vasileva. "Surface crystallography of complex and disordered surfaces." Thesis, University of Reading, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553057.

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Mansfield, Mark. "Surface stress and reconstructions on metal surfaces." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359866.

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Myshlyavtsev, Alexander V., and Marta D. Myshlyavtseva. "Modeling of surface diffusion for stepped surfaces." Universitätsbibliothek Leipzig, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-193477.

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Lee, Chee-kwan. "Modelling of flexible surfaces using a point mass system /." [Hong Kong : University of Hong Kong], 1992. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13204889.

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Zhang, Jinhong. "Surface Forces between Silica Surfaces in CnTACl Solutions and Surface Free Energy Characterization of Talc." Diss., Virginia Tech, 2006. http://hdl.handle.net/10919/29997.

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In general, the stability of suspension can be studied using two methods. One is to directly measure the forces between two interacting surfaces in media. The other is to study the interfacial surface free energies of the particles in suspension. Direct surface force measurements were conducted between silica surfaces in octadecyltrimetylammonium chloride (C₁₈TACl) solutions using an Atomic Force Microscope (AFM). The results showed that the hydrophobic force existed in both air-saturated and degassed C₁₈TACl solutions. The attraction decreased with NaCl addition, and was the strongest at the point of charge neutralization (p.c.n.) of silica substrate. The force measurement results obtained in C_nTACl solutions showed that the attractions decayed exponentially and became the maximum at the p.c.n.'s. The decay lengths (D) increased with surfactant chain length. The measured forces were fitted to a charged-patch model of Miklavic et al. (1994) with rather large patch sizes. It was also found that the decay length decreased linearly with the effective concentration of the CH2/CH3 groups raised to the power of -1/2. This finding is in line with the model of Eriksson et al. (1989). It suggested that the long-range attractions are hydrophobic forces originating from the changes in water structure across a hydrophobic surface-solution interface. For the TiO₂/water/TiO₂ system, the Hamaker constant was found to be 4±1×10^-20 J. The force curves obtained in the TiO₂/C_nTACl system showed a repulsion-attraction-repulsion transition with increasing surfactant concentration. The long-range attraction observed between TiO₂ surfaces in C_nTACl solutions reached maximum at the p.c.n., and the decay length increased with chain length. In present work, the thin-layer wicking technique was used to determine the surface free energy (γ_s) and its components of talc samples. The results showed that the basal surfaces of talc are weakly basic while the edge surfaces are acidic. The effect of chemicals on the surface free energies of talc was systemically studied. The results showed that CMC (carboxymethyl cellulose sodium salt) and EO/PO (ethylene oxide/propylene oxide) co-polymers made talc surface hydrophilic by increasing the surface free energies, especially γ^LW and γ^-. SOPA (sodium polyacrylate) increased greatly the zeta-potentials instead of the surface free energies.
Ph. D.

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Dalpé, Denis. "Schwarz's surface and the theory of minimal surfaces." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape15/PQDD_0023/MQ39958.pdf.

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Books on the topic "Surface"

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1933-, Neumann A. W., and Spelt Jan K. 1956-, eds. Applied surface thermodynamics. New York: M. Dekker, 1996.

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Hudson, John B. Surface science: An introduction. Boston: Butterworth-Heinemann, 1992.

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1936-, Nowotny Janusz, and Dufour Louis-Claude, eds. Surface and near-surface chemistry of oxide materials. Amsterdam: Elsevier, 1988.

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Wolf, Rory A. Plastic surface modification: Surface treatment and adhesion. Munich [Germany]: Hanser, 2010.

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1941-, Andrade Joseph D., and American Chemical Society. Rocky Mountain Regional Meeting, eds. Polymer surface dynamics. New York: Plenum Press, 1988.

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Wandelt, K. Surface and interface science. Weinheim: Wiley-VCH, 2012.

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Davison, Sydney G. Basic theory of surface states. New York: Clarendon Press, 1996.

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M, Walls J., and Smith R, eds. Surface science techniques. Oxford, England: Pergamon, 1994.

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B, Duke Charles, ed. Surface science: The first thirty years. Amsterdam: North-Holland, 1994.

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H, Clark R. J., and Hester R. E, eds. Spectroscopy for surface science. Chichester: Wiley, 1998.

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Book chapters on the topic "Surface"

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Karpfinger, Christian. "Surfaces and Surface Integrals." In Calculus and Linear Algebra in Recipes, 675–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65458-3_60.

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Fusco, Nicola, Paolo Marcellini, and Carlo Sbordone. "Surfaces and Surface Integrals." In UNITEXT, 525–66. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04151-8_10.

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Grzesik, Wit, Bogdan Kruszynski, and Adam Ruszaj. "Surface Integrity of Machined Surfaces." In Surface Integrity in Machining, 143–79. London: Springer London, 2010. http://dx.doi.org/10.1007/978-1-84882-874-2_5.

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Bulou, H., C. Goyhenex, and C. Massobrio. "Surface Diffusion on Inhomogeneous Surfaces." In Advances in the Atomic-Scale Modeling of Nanosystems and Nanostructured Materials, 123–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-04650-6_5.

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Raether, Heinz. "Surface plasmons on smooth surfaces." In Springer Tracts in Modern Physics, 4–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/bfb0048319.

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Wolf, Gert W. "Topographic Surfaces and Surface Networks." In Topological Data Structures for Surfaces, 13–29. Chichester, UK: John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/0470020288.ch2.

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Birdi, K. S. "Surface Chemistry of Solid Surfaces." In Surface Chemistry and Geochemistry of Hydraulic Fracturing, 87–117. Boca Raton : Taylor & Francis Group, 2017. | “A CRC title.”: CRC Press, 2016. http://dx.doi.org/10.1201/9781315372372-4.

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Hüfner, Stefan. "Surface States, Surface Effects." In Photoelectron Spectroscopy, 501–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-09280-4_8.

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Hüfner, Stefan. "Surface States, Surface Effects." In Springer Series in Solid-State Sciences, 367–402. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03209-1_8.

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Hüfner, Stefan. "Surface States, Surface Effects." In Springer Series in Solid-State Sciences, 367–402. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-662-03150-6_8.

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Conference papers on the topic "Surface"

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Elber, G., and Myung-Soo Kim. "A computational model for nonrational bisector surfaces: curve-surface and surface-surface bisectors." In Proceedings Geometric Modeling and Processing 2000. Theory and Applications. IEEE, 2000. http://dx.doi.org/10.1109/gmap.2000.838267.

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Pregliasco, R. G., J. E. Gayone, E. A. Sánchez, and O. Grizzi. "TOF-Ion scattering spectrometer for surface analysis: Application to a GaAs (110) surface." In The 8th Latin American congress on surface science: Surfaces , vacuum, and their applications. AIP, 1996. http://dx.doi.org/10.1063/1.51182.

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Zhang, F. S., R. H. Wang, H. A. Macleod, R. E. Parks, and M. R. Jacobson. "Surface Plasmon Detection Of Surface Contamination Of Metallic Film Surfaces." In Technical Symposium Southeast, edited by A. Peter M. Glassford. SPIE, 1987. http://dx.doi.org/10.1117/12.967076.

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Sámano, E. C., and W. E. Carr. "Atom flux measurement by surface ionization." In The 8th Latin American congress on surface science: Surfaces , vacuum, and their applications. AIP, 1996. http://dx.doi.org/10.1063/1.51178.

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Thoemel, Jan, and Olivier Chazot. "Surface Catalysis of Rough Surfaces." In 41st AIAA Thermophysics Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2009. http://dx.doi.org/10.2514/6.2009-3931.

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Ratner, Buddy D., and David G. Castner. "Surface analysis for biomaterials and biological systems." In The 8th Latin American congress on surface science: Surfaces , vacuum, and their applications. AIP, 1996. http://dx.doi.org/10.1063/1.51193.

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Velasco, P. A., V. A. Bustos, and G. Zgrablich. "Multilayer adsorption with surface reconstruction: A simple model." In The 8th Latin American congress on surface science: Surfaces , vacuum, and their applications. AIP, 1996. http://dx.doi.org/10.1063/1.51162.

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Weisz, S. Z., J. Avalos, M. Gomez, A. Many, Y. Goldstein, and E. Savir. "Bulk and surface states on hydrogenated amorphous silicon." In The 8th Latin American congress on surface science: Surfaces , vacuum, and their applications. AIP, 1996. http://dx.doi.org/10.1063/1.51116.

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Irusta, S., L. M. Cornaglia, E. E. Miró, and E. A. Lombardo. "Surface characterization of vanadium on silica (V/SiO2) catalysts." In The 8th Latin American congress on surface science: Surfaces , vacuum, and their applications. AIP, 1996. http://dx.doi.org/10.1063/1.51152.

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Garland, P. P., and R. J. Rogers. "Progress on experimental and finite element studies of oblique elastic impact." In CONTACT/SURFACE 2007. Southampton, UK: WIT Press, 2007. http://dx.doi.org/10.2495/secm070161.

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Reports on the topic "Surface"

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Whitman, P., J. DeYoreo, T. Land, E. Miller, T. Suratwala, C. Thorsness, and E. Wheeler. Surface Dynamics during Environmental Degradation of Crystal Surfaces. Office of Scientific and Technical Information (OSTI), February 2001. http://dx.doi.org/10.2172/15013517.

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Yang, S. L., D. Oryang, and M. J. Ho. A surface definition code for turbine blade surfaces. Office of Scientific and Technical Information (OSTI), May 1992. http://dx.doi.org/10.2172/10146608.

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De Yoreo, J., and I. Smolsky. Surface dynamics during environmental degradation of crystal surfaces. Office of Scientific and Technical Information (OSTI), April 1999. http://dx.doi.org/10.2172/10791.

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Yang, S. L., D. Oryang, and M. J. Ho. A surface definition code for turbine blade surfaces. Office of Scientific and Technical Information (OSTI), May 1992. http://dx.doi.org/10.2172/5246536.

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White, Brandy J., Martin H. Moore, and Anthony P. Malanoski. Bioinspired Surface Treatments for Improved Decontamination: Icephobic Surfaces. Fort Belvoir, VA: Defense Technical Information Center, June 2017. http://dx.doi.org/10.21236/ad1036844.

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Goldman, N., and R. G. Mullen. Conducting quantum simulations of surface reactivity on actinide surfaces. Office of Scientific and Technical Information (OSTI), November 2018. http://dx.doi.org/10.2172/1490949.

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Wang, Qing. Shipboard Measurements of Surface Flux and Near Surface Profiles and Surface Flux Parameterization. Fort Belvoir, VA: Defense Technical Information Center, September 2010. http://dx.doi.org/10.21236/ada542627.

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Wang, Qing. Shipboard Measurements of Surface Flux and Near Surface Profiles and Surface Flux Parameterization. Fort Belvoir, VA: Defense Technical Information Center, September 2012. http://dx.doi.org/10.21236/ada590698.

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Slattery, Kevin. Unsettled Topics on Surface Finishing of Metallic Powder Bed Fusion Parts in the Mobility Industry. SAE International, January 2021. http://dx.doi.org/10.4271/epr2021001.

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Abstract:

Laser and electron-beam powder bed fusion (PBF) additive manufacturing (AM) technology has transitioned from prototypes and tooling to production components in demanding fields such as medicine and aerospace. Some of these components have geometries that can only be made using AM. Initial applications either take advantage of the relatively high surface roughness of metal PBF parts, or they are in fatigue, corrosion, or flow environments where surface roughness does not impose performance penalties. To move to the next levels of performance, the surfaces of laser and electron-beam PBF components will need to be smoother than the current as-printed surfaces. This will also have to be achieve on increasingly more complex geometries without significantly increasing the cost of the final component. Unsettled Topics on Surface Finishing of Metallic Powder Bed Fusion Parts in the Mobility Industry addresses the challenges and opportunities of this technology, and what remains to be agreed upon by the industry.

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Campion, Alan. In-Situ Surface during Laser-Controlled Chemical Processing of Surfaces. Fort Belvoir, VA: Defense Technical Information Center, June 1988. http://dx.doi.org/10.21236/ada200206.

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