Academic literature on the topic 'Thermal Expansion'

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Journal articles on the topic "Thermal Expansion"

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Miyagawa, Azusa, Shogo Nobukawa, and Masayuki Yamaguchi. "Thermal Expansion Behavior of Antiplasticized Polycarbonate." Nihon Reoroji Gakkaishi 42, no. 4 (2014): 255–60. http://dx.doi.org/10.1678/rheology.42.255.

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LI, Z., and R. C. BRADT. "Thermal Expansion and Thermal Expansion Anisotropy of SiC Polytypes." Journal of the American Ceramic Society 70, no. 7 (July 1987): 445–48. http://dx.doi.org/10.1111/j.1151-2916.1987.tb05673.x.

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Thiéblot, Laurent, Jacques Roux, and Pascal Richet. "High-temperature thermal expansion and decomposition of garnets." European Journal of Mineralogy 10, no. 1 (January 26, 1998): 7–16. http://dx.doi.org/10.1127/ejm/10/1/0007.

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Jackson, Jennifer M., James W. Palko, Denis Andrault, Stanislav V. Sinogeikin, Dmitry L. Lakshtanov, Jingyun Wang, Jay D. Bass, and Chang-Sheng Zha. "Thermal expansion of natural orthoenstatite to 1473 K." European Journal of Mineralogy 15, no. 3 (June 10, 2003): 469–73. http://dx.doi.org/10.1127/0935-1221/2003/0015-0469.

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Barrera, G. D., J. A. O. Bruno, T. H. K. Barron, and N. L. Allan. "Negative thermal expansion." Journal of Physics: Condensed Matter 17, no. 4 (January 15, 2005): R217—R252. http://dx.doi.org/10.1088/0953-8984/17/4/r03.

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Fakhruddin, Hasan. "Thermal expansion ‘‘paradox’’." Physics Teacher 31, no. 4 (April 1993): 214. http://dx.doi.org/10.1119/1.2343727.

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Küchler, R., P. Gegenwart, K. Heuser, E. W. Scheidt, G. R. Stewart, and F. Steglich. "Thermal expansion of." Physica B: Condensed Matter 359-361 (April 2005): 53–55. http://dx.doi.org/10.1016/j.physb.2004.12.054.

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Haverland, Gordon Wayne. "Thermal expansion coefficient." JOM 49, no. 8 (August 1997): 6. http://dx.doi.org/10.1007/bf02914380.

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AZUMA, Masaki. "Zero-Thermal Expansion Composite with Giant Negative Thermal Expansion Powder." Hosokawa Powder Technology Foundation ANNUAL REPORT 23 (2015): 18–22. http://dx.doi.org/10.14356/hptf.13101.

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Lim, Teik-Cheng. "Negative thermal expansion structures constructed from positive thermal expansion trusses." Journal of Materials Science 47, no. 1 (July 28, 2011): 368–73. http://dx.doi.org/10.1007/s10853-011-5806-z.

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Dissertations / Theses on the topic "Thermal Expansion"

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Miller, Wayne. "Negative Thermal Expansion Materials." Thesis, University of Exeter, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531676.

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Hansen, Glenn Alexander. "TWO ULTRAPRECISE THERMAL EXPANSION INVESTIGATIONS: SODIUM SILICATE - A LOW-EXPANSION CEMENT, AND THERMAL EXPANSION UNIFORMITY OF ZERODUR." Thesis, The University of Arizona, 1985. http://hdl.handle.net/10150/291814.

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Maksimova, E. M., and A. I. Zamkovskaya. "Visualization of Thermal Crystals Expansion." Thesis, Sumy State University, 2015. http://essuir.sumdu.edu.ua/handle/123456789/40672.

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Greyling, Guillaume Hermanus. "Negative thermal expansion of organic compounds." Thesis, Stellenbosch : Stellenbosch University, 2011. http://hdl.handle.net/10019.1/6896.

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Thesis (MSc)--Stellenbosch University, 2011.
ENGLISH ABSTRACT: The primary objective of the work was to investigate the negative thermal expansion of organic materials and to determine the mechanisms governing this phenomenon by using the principles of crystal engineering. To this end, the following three compounds were studied in detail: • 4,4'-Diiodobiphenyl • 4-Iodobenzoic acid • Methyl Paraben The rationale behind this work was to determine the mechanisms responsible for the observed negative thermal expansion and to uncover the structural factors that induce negative thermal expansion. Single-crystal X-ray diffraction was employed as the primary analytical tool, owing to the unique information it can provide regarding intermolecular interactions in the solid state. A total of twenty organic compounds were analysed, of which three exhibited negative thermal expansion. Each compound employs a specific mechanism for negative thermal expansion, two of which are closely related and the third distinct.
AFRIKAANSE OPSOMMING: Die hoof doel van hierdie studie was om ondersoek in te stel in die verskynsel van ‘negative thermal expansion’ in organiese materiale en gevolglik die meganisme vas te stel deur die beginsels van kristalmanipulsie (‘crystal engineering’) te gebruik. Gevolglik was drie organise stowwe ondersoek: • 4,4'-Diiodobiphenyl /4,4'-Diiodobifeniel • 4-Iodobenzoic acid /4-Iodobensoësuur • Methyl Paraben Die redenasie hieragter is om die meganisme verantwoordelik vir die ‘negative thermal expansion’ vas te stel en die verskillende faktore wat bydra tot dit te bevestig. Enkel-kristal diffraksie word benut as die primêre analitiese tegniek as gevolg van die unieke inligting wat verkry kan word met betrekking tot die intermolekulêre interaksies. 'n Totaal van twintig stowwe is geanaliseer waarvan drie die spesifieke termisie eienskap besit. Elk van die drie stowwe het ‘n ander meganisme te vore laat kom waarvan twee baie ooreenstem en die derde verskil.
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Tu, Jie. "Thermal expansion of chemically modified mullite." Thesis, Virginia Tech, 1988. http://hdl.handle.net/10919/43063.

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Solid-state reaction and sol-gel, processing techniques were used extensively to form chemically-modified mullite solid solutions in an effort to lower their thermal expansion coefficients. TiO2, B203, CrPO4, P205, Ga203, Cr203, and WO3 and the half-breed Si02 compounds AlPas, BPO4, GaPO4, BAsO4, AIAsO4, GaAsO4, and Ge02 were chosen as the modifiers. The results indicate that, apart from Ti02, none of the substitutions made in mullite significantly change the thermal expansion properties. The solubility of 3 wt% TiO2 in mullite reduces the coefficient of thermal expansion by about 10%; That corresponds to a reduction in A1203/Si02 molar ratio ( < 1.5) compared to stoichiometric mullite (3A1203⠢2Si02). The formation of Ti02-modified mullite depends on processing condition and heat treatment. The possible mechanism of lowering the CTE of mullite by the addition of TiO2 is discussed in terms of the bond strength. The axial expansion of a Ga203-modified mullite was measured' up to 1200°C to show that the expansion is increased along the c-axis compared with that of the stoichiometric mullite.
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Greve, Benjamin K. "Exploring the thermal expansion of fluorides and oxyfluorides with ReO₃-type structures: from negative to positive thermal expansion." Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/43753.

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This thesis explores the thermal expansion and high pressure behavior of some materials with the ReO₃ structure type. This structure is simple and has, in principle, all of the features necessary for negative thermal expansion (NTE) arising from the transverse thermal motion of the bridging anions and the coupled rotation of rigid units; however, ReO₃ itself only exhibits mild NTE across a narrow temperature range at low temperatures. ReO₃ is metallic because of a delocalized d-electron, and this may contribute to the lack of NTE in this material. The materials examined in this thesis are all based on d⁰ metal ions so that the observed thermal expansion behavior should arise from vibrational, rather than electronic, effects. In Chapter 2, the thermal expansion of scandium fluoride, ScF₃, is examined using a combination of in situ synchrotron X-ray and neutron variable temperature diffraction. ScF₃ retains the cubic ReO₃ structure across the entire temperature range examined (10-1600 K) and exhibits pronounced negative thermal expansion at low temperatures. The magnitude of NTE in this material is comparable to that of cubic ZrW₂O₈, which is perhaps the most widely studied NTE material, at room temperature and below. This is the first report of NTE in an ReO₃ type structure across a wide temperature range. Chapter 3 presents a comparison between titanium oxyfluoride, TiOF₂, and a vacancy containing titanium hydroxyoxyfluoride, Tiₓ(O/OH/F)₃. TiOF₂ was originally reported to adopt the cubic ReO₃ structure type under ambient conditions, therefore the initial goal for this study was to examine the thermal expansion of this material and determine if it displayed interesting behavior such as NTE. During the course of the study, it was discovered that the original synthetic method resulted in Tiₓ(O/OH/F)₃, which does adopt the cubic ReO₃ structure type. The chemical composition of the hydroxyoxyfluoride is highly dependent upon synthesis conditions and subsequent heat treatments. This material readily pyrohydrolyizes at low temperatures (~350 K). It was also observed that TiOF₂ does not adopt the cubic ReO₃ structure; at room temperature it adopts a rhombohedrally distorted variant of the ReO₃ structure. Positive thermal expansion was observed for TiOF₂ from 120 K through decomposition into TiO₂. At ~400 K, TiOF₂ undergoes a structural phase transition from rhombohedral to cubic symmetry. High pressure diffraction studies revealed a cubic to rhombohedral phase transition for Tiₓ(O/OH/F)₃ between 0.5-1 GPa. No phase transitions were observed for TiOF₂ on compression. In Chapter 4, an in situ variable pressure{temperature diffraction experiment examining the effects of pressure on the coefficients of thermal expansion (CTE) for ScF₃ and TaO₂F is presented. In the manufacture and use of composites, which is a possible application for low and NTE materials, stresses may be experienced. Pressure was observed to have a negligible effect on cubic ScF₃'s CTE; however, for TaO₂F the application of modest pressures, such as those that might be experienced in the manufacture or use of composites, has a major effect on its CTE. This effect is associated with a pressure-induced phase transition from cubic to rhombohedral symmetry upon compression. TaO₂F was prepared from the direct reaction of Ta₂O₅ with TaF₅ and from the digestion of Ta₂O₅ in hot hydro uoric acid. The effects of pressure on the two samples of TaO₂F were qualitatively similar. The slightly different properties for the samples are likely due to differences in their thermal history leading to differing arrangements of oxide and uoride in these disordered materials. In Chapter 5, the local structures of TiOF₂ and TaO₂F are examined using pair distribution functions (PDFs) obtained from X-ray total scattering experiments. In these materials, the anions (O/F) are disordered over the available anion positions. While traditional X-ray diffraction provides detailed information about the average structures of these materials, it is not suffcient to fully understand their thermal expansion. Fits of simple structural models to the low r portions of PDFs for these materials indicate the presence of geometrically distinct M{X{M (M = Ti, Ta; X = O, F) linkages, and a simple analysis of the TaO₂F variable temperature PDFs indicates that these distinct links respond differently to temperature.
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Ruschman, Chad. "Chemical tuning of thermal expansion in oxides." Thesis, Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/34778.

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This work focuses on the chemical substitution of cations and anions in the frameworks of materials that have been known to exhibit negative thermal expansion (NTE). Zr2(PO4)2(SO4) is a member of the A(2)M(3)O(12) family which has been known to exhibit NTE. We have shown that Zr2(PO4)2(SO4) exhibits anisotropic positive thermal expansion. We have also shown that this material has been characterized in the wrong space group. Hf2(PO4)2(SO4) behaves similarly to Zr2(PO4)2(SO4) and follows this trend. Under pressure, Hf2(PO4)2(SO4) appears to undergo a phase transition. We have still yet to determine what space group the materials transitions to. While many members of the AX(2)O(7) family of frameworks have been fully characterized, the thermal expansion of PbP2O7 has yet to be reported. We were unable to obtain a reproducible procedure for synthesis of PbP2O7 from its precursor. Finally, variable temperature and variable pressure studies were performed on ZrMo2O8 in an attempt to learn more about the local structure. We found that space groups P213 and Pa-3 gave poor fits of the local structure at low r. Behavior of the nearest neighbor Zr-Mo distance was very similar to the bulk CTE. On compression, pressure induced amorphization is observed in ZrMo2O8. All interatomic correlations above 4 angstroms are washed out. Zr-O-Mo linkages remain well defined and do not massively deform as the pressure is increased. Finally, we we observed that Zr-O-Mo linkages change geometry reversibly as the pressure is increased.
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Mackenzie, D. S. "Modeling negative thermal expansion in network structures." Thesis, University of Exeter, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.441808.

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Rimmer, Leila Heather Najla. "Negative thermal expansion in flexible framework materials." Thesis, University of Cambridge, 2014. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.707927.

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Lind, Cora. "Negative thermal expansion materials related to cubic zirconium tungstate." Diss., Georgia Institute of Technology, 2001. http://hdl.handle.net/1853/30861.

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Books on the topic "Thermal Expansion"

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1928-, Ho C. Y., and Taylor R. E. 1934-, eds. Thermal expansion of solids. Materials Park, OH: ASM International, 1998.

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Bach, Hans, ed. Low Thermal Expansion Glass Ceramics. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-662-03083-7.

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Bach, Hans, and Dieter Krause, eds. Low Thermal Expansion Glass Ceramics. Berlin/Heidelberg: Springer-Verlag, 2005. http://dx.doi.org/10.1007/3-540-28245-9.

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1930-, Bach Hans, and Krause Dieter 1933-, eds. Low thermal expansion glass ceramics. 2nd ed. Berlin: Springer, 2005.

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1930-, Bach Hans, ed. Low thermal expansion glass ceramics. Berlin: Springer, 1995.

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Ellis, David L. Thermal conductivity and thermal expansion of graphite fiber/copper matrix composites. [Washington, DC]: National Aeronautics and Space Administration, 1991.

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radiomettalurgist, Sengupta A. K., and Bhabha Atomic Research Centre, eds. Thermal expansion data of (Th,U)O2 fuels. Mumbai: Bhabha Atomic Research Centre, 2000.

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Barron, T. H. K. Heat capacity and thermal expansion at low temperatures. New York: Kluwer Academic/Plenum, 1999.

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Barron, T. H. K., and G. K. White. Heat Capacity and Thermal Expansion at Low Temperatures. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4695-5.

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Jackson, Douglas Anthony. The thermal expansion characteristics of fibre reinforced thermoplastics. Salford: University of Salford, 1989.

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Book chapters on the topic "Thermal Expansion"

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Hummel, Rolf E. "Thermal Expansion." In Electronic Properties of Materials, 291–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-662-02424-9_22.

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Hummel, Rolf E. "Thermal Expansion." In Electronic Properties of Materials, 358–60. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-017-4914-5_22.

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Ventura, Guglielmo, and Mauro Perfetti. "Thermal Expansion." In Thermal Properties of Solids at Room and Cryogenic Temperatures, 81–91. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-8969-1_4.

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Hummel, Rolf E. "Thermal Expansion." In Electronic Properties of Materials, 397–99. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-86538-1_22.

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Mörner, Nils-Axel. "Thermal Expansion." In Encyclopedia of Earth Sciences Series, 1692–94. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-93806-6_375.

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Gooch, Jan W. "Thermal Expansion." In Encyclopedic Dictionary of Polymers, 741–42. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11747.

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Mörner, Nils-Axel. "Thermal Expansion." In Encyclopedia of Earth Sciences Series, 1–3. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-48657-4_375-1.

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Janssen, Jules J. A. "Thermal expansion." In Mechanical Properties of Bamboo, 11. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3236-7_2.

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Godovsky, Yuli K. "Thermal Expansion." In Thermophysical Properties of Polymers, 75–106. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-51670-2_3.

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Fei, Yingwei. "Thermal Expansion." In AGU Reference Shelf, 29–44. Washington, D. C.: American Geophysical Union, 2013. http://dx.doi.org/10.1029/rf002p0029.

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Conference papers on the topic "Thermal Expansion"

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GOETZE, PITT, SIMON HUMMEL, RHENA WULF, TOBIAS FIEBACK, and ULRICH GROSS. "Challenges of Transient-Plane-Source Measurements at Temperatures Between 500K and 1000K." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30332.

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HUME, DALE, ANDREY SIZOV, BESIRA M. MIHIRETIE, DANIEL CEDERKRANTZ, SILAS E. GUSTAFSSON, and MATTIAS K. GUSTAVSSON. "Specific Heat Measurements of Large-Size Samples with the Hot Disk Thermal Constants Analyser." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30333.

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SONG, ZHUORUI, TYSON WATKINS, and HENG BAN. "Measurement of Thermal Diffusivity at High Temperature by Laser Flash Method." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30334.

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CASTIGLIONE, PAOLO, and GAYLON CAMPBELL. "Improved Transient Method Measures Thermal Conductivity of Insulating Materials." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30335.

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GARDNER, LEVI, TROY MUNRO, EZEKIEL VILLARREAL, KURT HARRIS, THOMAS FRONK, and HENG BAN. "Laser Flash Measurements on Thermal Conductivity of Bio-Fiber (Kenaf) Reinforced Composites." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30336.

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DEHN, SUSANNE, ERIK RASMUSSEN, and CRISPIN ALLEN. "Round Robin Test of Thermal Conductivity for a Loose Fill Thermal Insulation Product in Europe." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30337.

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ILLKOVA, KSENIA, RADEK MUSALEK, and JAN MEDRICKY. "Measured and Predicted Thermal Conductivities for YSZ Layers: Application of Different Models." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30338.

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LAGER, DANIEL, CHRISTIAN KNOLL, DANNY MULLER, WOLFGANG HOHENAUER, PETER WEINBERGER, and ANDREAS WERNER. "Thermal Conductivity Measurements of Calcium Oxalate Monohydrate as Thermochemical Heat Storage Material." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30339.

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YARBROUGH, DAVID W., and MICHEL P. DROUIN. "Long-Term Thermal Resistance of Thin Cellular Plastic Insulations." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30340.

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KANTHARAJ, RAJATH, ISHAN SRIVASTAVA, AMY M. MARCONNET, and TIMOTHY S. FISHER. "Granular Jamming and Thermal Modeling in Faceted Particle Packings." In Thermal Conductivity 33/Thermal Expansion 21. Lancaster, PA: DEStech Publications, Inc., 2019. http://dx.doi.org/10.12783/tc33-te21/30341.

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Reports on the topic "Thermal Expansion"

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Menikoff, Ralph. Thermal Expansion of PBX 9502. Office of Scientific and Technical Information (OSTI), June 2018. http://dx.doi.org/10.2172/1441276.

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Schonfeld, F. W., and R. E. Tate. The thermal expansion behavior of unalloyed plutonium. Office of Scientific and Technical Information (OSTI), September 1996. http://dx.doi.org/10.2172/385588.

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Tucker, Laura, and Philip Schembri. Calculating the Secant Coefficient of Thermal Expansion. Office of Scientific and Technical Information (OSTI), February 2023. http://dx.doi.org/10.2172/1924392.

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Thompson, Darla Graff, and Racci DeLuca. Coefficient of Thermal Expansion of Pressed PETN Pellets. Office of Scientific and Technical Information (OSTI), March 2015. http://dx.doi.org/10.2172/1172824.

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Berthelot, Y. Laser Generation of Sound by Nonlinear Thermal Expansion. Fort Belvoir, VA: Defense Technical Information Center, February 1994. http://dx.doi.org/10.21236/ada276955.

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Kautz, D. D., R. L. Sites, and W. R. Cobb. WPH-6112A thermal expansion test of PRESS tubulation. Office of Scientific and Technical Information (OSTI), May 1994. http://dx.doi.org/10.2172/10170478.

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C.B. Skidmore, T.A. Butler, and C.W. Sandoval. The Elusive Coefficients of Thermal Expansion in PBX 9502. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/809945.

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Eash, D. T. Cryogenic Thermal Expansion of Y-12 Graphite Fuel Elements. Office of Scientific and Technical Information (OSTI), July 2013. http://dx.doi.org/10.2172/1087006.

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Thompson, Darla Graff, Caitlin Savanna Woznick, and Racci DeLuca. The Volumetric Coefficient of Thermal Expansion of PBX 9502. Office of Scientific and Technical Information (OSTI), March 2018. http://dx.doi.org/10.2172/1425787.

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Feng, W., and T. Hoheisel. Coefficients of thermal expansion for a carbon-carbon composite. Office of Scientific and Technical Information (OSTI), November 1989. http://dx.doi.org/10.2172/5244635.

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