Relevant bibliographies by topics / Solids

Academic literature on the topic 'Solids'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 July 2024

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Journal articles on the topic "Solids"

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Houot, Robert. "Séparation solide-solide. / Separation between solids." Sciences Géologiques. Bulletin 46, no. 1 (1993): 125–41. http://dx.doi.org/10.3406/sgeol.1993.1900.

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Gai, Pratibha L., and Michael W. Anderson. "Solid catalysts and porous solids." Current Opinion in Solid State and Materials Science 5, no. 5 (October 2001): 363–64. http://dx.doi.org/10.1016/s1359-0286(01)00033-x.

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Gai, Pratibha L., and Michael W. Anderson. "Solid catalysts and porous solids." Current Opinion in Solid State and Materials Science 6, no. 5 (October 2002): 379. http://dx.doi.org/10.1016/s1359-0286(02)00121-3.

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Davis, MarkE, and IanE Maxwell. "Solid catalysts and porous solids." Current Opinion in Solid State and Materials Science 1, no. 1 (February 1996): 55–56. http://dx.doi.org/10.1016/s1359-0286(96)80010-6.

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Zones, Stacey, and Ian E. Maxwell. "Solid catalysts and porous solids." Current Opinion in Solid State and Materials Science 2, no. 1 (February 1997): 55–56. http://dx.doi.org/10.1016/s1359-0286(97)80105-2.

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Cheetham, Anthony K., and Sir John Meurig Thomas. "Solid catalysts and porous solids." Current Opinion in Solid State and Materials Science 3, no. 1 (February 1998): 61–62. http://dx.doi.org/10.1016/s1359-0286(98)80066-1.

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Anderson, Michael W. "Solid catalysts and porous solids." Current Opinion in Solid State and Materials Science 7, no. 3 (June 2003): 189. http://dx.doi.org/10.1016/j.cossms.2003.10.002.

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Anderson, M. W. "Solid Catalysts and Porous Solids." Current Opinion in Solid State and Materials Science 8, no. 6 (December 2004): 396. http://dx.doi.org/10.1016/j.cossms.2005.05.001.

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Davies, J. W., D. Butler, J. L. Small, V. Sekuloski, and C. Jefferies. "Gross solids transport and degradation." Water Science and Technology 37, no. 1 (January 1, 1998): 61–68. http://dx.doi.org/10.2166/wst.1998.0016.

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The paper describes the first stages of a study of the origin, transport, and fate of sewer gross solids. The background to the project, its overall plan, and relevant previous studies are outlined. Progress to-date is described. A laboratory study of physical degradation of gross solids has confirmed general existing field observations that many sanitary solids undergo little degradation, whereas toilet paper and faeces are readily degraded. A study of solid advection and deposition in a laboratory pipe system has covered a wide variety of sanitary and artificial solids. The velocity at which sanitary solids are advected with the flow has been observed to be similar for most solids in spite of a considerable range of shapes and sizes. Pipe-full conditions, introducing the retarding effect of the pipe wall at the soffit, have tended to reduce solid velocities especially for floating solids. Generally the advective velocity of artificial solids of the same material and shape has not varied significantly with solid size. However size has had a clearer influence on deposition: with decreasing size, solids of the same density have been deposited at lower values of depth and velocity.
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TARASOV, VASILY E. "DYNAMICS OF FRACTAL SOLIDS." International Journal of Modern Physics B 19, no. 27 (October 30, 2005): 4103–14. http://dx.doi.org/10.1142/s0217979205032656.

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We describe the fractal solid by a special continuous medium model. We propose to describe the fractal solid by a fractional continuous medium model, where all characteristics and fields are defined everywhere in the volume but they follow some generalized equations which are derived by using fractional integrals of fractional order. The order of fractional integral can be equal to the fractal mass dimension of the solid. Fractional integrals are considered as an approximation of integrals on fractals. We suggest the approach to compute the moments of inertia for fractal solids. The dynamics of fractal solids are described by the usual Euler's equations. The possible experimental test of continuous medium model for fractal solids is considered.
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Dissertations / Theses on the topic "Solids"

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Pradhan, Sulolit. "Solid state charge transfer in nanoparticle solids /." Diss., Digital Dissertations Database. Restricted to UC campuses, 2008. http://uclibs.org/PID/11984.

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Liu, Weidong. "High density solids downflow gas-solids reactors." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0001/MQ42081.pdf.

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Pinto, Maria do Rosario. "Perfect solids." Thesis, University of Southampton, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358006.

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Tian, Jian Atwood J. L. "Molecular organic solids for gas adsorption and solid-gas interaction." Diss., Columbia, Mo. : University of Missouri--Columbia, 2009. http://hdl.handle.net/10355/6882.

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Title from PDF of title page (University of Missouri--Columbia, viewed on Feb 24, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Dissertation advisor: Dr. Jerry L. Atwood. Vita. Includes bibliographical references.
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Yang, Wei. "Solids phase chromatography." Thesis, University of Leeds, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.505060.

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The present study focuses on the development of a novel technique, namely Solids Phase Chromatography (SPC), for particle classification and size analysis. SPC is a fractionation based technique and utilises a separation channel to fractionate the particle samples into sub-fractions according to their sizes. Subsequently, the products may be analysed by various detectors and recovered for other investigations.
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Mitchell, Martin R. "Investigation of structure and disorder in inorganic solids using solid-state NMR." Thesis, University of St Andrews, 2013. http://hdl.handle.net/10023/3367.

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The use of solid-state NMR and DFT calculations to study Y₂Sn[subscript(x)]Ti[subscript(2-x)]O₇, Y₂Sn[subscript(x)]Zr[subscript(2-x)]O₇ and Y₂Ti[subscript(x)]Zr[subscript(2-x)]O₇, materials with applications for the safe encapsulation of radioactive actinides is investigated. As a result of cation or anion disorder in these materials, NMR spectra are often complex and difficult to interpret. Therefore, an investigation using a range of NMR active nuclei and measurement of a variety of NMR parameters (isotropic chemical shift, δ[subscript(iso)]; span, Ω and quadrupolar coupling, C[subscript(Q)]) were used to provide a full and detailed picture of each material. The measurement of Ω in these disordered compounds with multiple resonances in the NMR spectra, required the use of 2D CSA-amplified PASS (CAPASS) experiments to enable the separation of each of the spinning sideband manifolds. An experimental assessment of the CAPASS experiment showed that although low ν₁/Ω[subscript(Hz)] ratios (as found in ⁸⁹Y NMR) resulted in distortions in the spectra obtained, a modified fitting procedure could be utilised to compensate for this fact, which allowed the accurate measurement of Ω. Despite the difficulties in acquiring the ⁸⁹Y NMR spectra, they were found to be the most informative of the NMR-active nuclei available. ¹¹⁹Sn NMR spectra, although much easier to acquire than ⁸⁹Y, were more complex and harder to analyse, owing to the overlapping resonances. Therefore, ¹¹⁹Sn NMR could only be used to confirm or support the results obtained using ⁸⁹Y NMR. Although ¹⁷O NMR was found to be useful, a full study could not be implemented due to the lack of ¹⁷O enriched samples; an area where future investigation may prove fruitful. Finally, [superscript(47/49)]Ti and ⁹¹Zr NMR spectra were found to be the most difficult to acquire due to their low receptivities and the quadrupolar broadened lineshapes, and as a result, little additional information was obtained. As a result of this analysis, for the Y₂Sn[subscript(x)]Ti[subscript(2-x)]O₇ pyrochlore solid solution, using primarily ⁸⁹Y δ[subscript(iso)] and Ω, and additionally confirmed with ¹¹⁹Sn δ[subscript(iso)], it was found that the Sn and Ti cations were randomly ordered throughout the B-sites. Additionally, ⁸⁹Y Ω could be used to obtain approximate Y-O[subscript(48f)] and Y-O[subscript(8b)] bond lengths for each type of Y environment. The study of Y₂Sn[subscript(x)]Zr[subscript(2-x)]O₇ using ⁸⁹Y NMR showed that although the end members were single phase, pyrochlore (Y₂Sn₂O₇) or defect fluorite (Y₂Zr₂O₇), the intermediate compositions were mostly two phase mixtures, consisting of an ordered pyrochlore (with an average formula of Y₂Sn₁.₈Zr₀.₂O₇) and a disordered phase, where the proportions of the pyrochlore and disordered phases decreased and increased, respectively, with the Zr content. Additionally, although the coordination states of the Y and Sn cations were easily determined using ⁸⁹Y and ¹¹⁹Sn NMR, respectively, the coordination states of the Zr cations could not be confirmed directly by ⁹¹Zr NMR. However, using indirect analysis from results obtained with ⁸⁹Y and ¹¹⁹Sn NMR, it was determined that 6 coordinate Zr was present in each composition, and it was always present in a greater proportion than 8 coordinate Zr. Finally, although ⁸⁹Y NMR spectra of Y₂Ti[subscript(x)]Zr[subscript(2-x)]O₇ were extremely difficult to analyse, it was tentatively proposed that they could be similar to Y₂Sn[subscript(x)]Zr[subscript(2-x)]O₇ due to some similarities observed between the spectra.
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Cockroft, Nigel J. "Solid state spectroscopy : laser selective excitation of erbium ions in crystalline solids." Thesis, University of Canterbury. Physics, 1987. http://hdl.handle.net/10092/8056.

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Optical absorption and laser selective excitation (l.s.e.) spectroscopy have been used to study Er³⁺ ions in the CsCdBr₃ and hydrogenated CaF₂ and SrF₂ crystalline lattices. Sixteen hydrogenic charge compensation sites for both the H- and D- isotopes were found in CaF₂:0.05%Er³⁺, and nine new D- ion sites in SrF₂ :0.05%Er3³⁺. The relative occurrence of these sites can be controlled by variation of the duration of hydrogenation. For SrF₂:Er³⁺, this results in a change of the principal D- ion charge compensation arrangement. Classification of local-mode vibronic fluorescence transitions and consideration of isotope shifts of electronic transitions enabled the assignment of model configurations to several sites. Most hydrogenic sites were classified into one of two distinct families. A new effect, reversible polarised bleaching was observed, whereby hydrogenic ion migration in Er³⁺ ion site configurations can be controlled by l.s.e. with polarised light in oriented crystals. One hydrogenic site was found to consist of two photo-induced interconvertible components. Five new fluoride ion sites in CaF₂:Er³⁺ and nine in SrF₂:Er³⁺ were also determined. For <100> and <111> oriented crystals, the fluorescence spectra of several sites exhibited well defined polarisation which may be used to determine the Er³⁺ ion symmetry. Trigonal symmetry of the F- B site of CaF₂:Er³⁺ was confirmed by this means. Crystal field analysis of tetragonal and trigonal symmetry sites is also reported. An infra-red study revealed local mode lines of seven new sites in hydrogenated CaF₂:Er³⁺ and enabled correlation of some sites to those observed in the optical spectra. Reduction of Er³⁺ ions by the short range beta decay of tritium in the lattice was identified by local mode absorption. Erbium ions in CsCdBr₃ exhibited efficient upconverted fluorescence consistent with the formation of a dominant dimer site. Detailed spectroscopy resulted in the assignment of energy levels from twelve groups of transitions. Several of these transitions, studied by absorption and l.s.e., were found to consist of two components.
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Mujaji, Marjorie. "Solid state spectroscopy : laser selective excitation of holmium ions in crystalline solids." Thesis, University of Canterbury. Physics, 1992. http://hdl.handle.net/10092/8145.

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The technique of laser selective excitation has been used to study the spectra of 23 Ho³⁺centres present in CaF₂ and SrF₂ crystals, in mixed Ca₀.₉₉Sr₀.₀₁F₂ and Ca₀.₉₉Ba₀.₀₁F₂ crystals and in CsCdBr₃ crystals. The polarisation of the fluorescence from < 100> and < 111> oriented crystals has been used to assign specific Ho³⁺ site symmetries to the various centres and to label the crystal-field energy levels of each centre by their group irreps. The two principal Ho³⁺ centres (A and B) observed in both CaF2:Ho³⁺and SrF2:Ho³⁺ crystals have been shown to be of C₄ᵥ and C₃ᵥ symmetry respectively. The four new centres identified in Ca₀.₉₉Sr₀.₀₁F₂:Ho3³⁺ and Ca₀.₉₉Ba₀.₀₁F₂:Ho³⁺ crystals, are derived from the parent CaF₂ C₄ᵥ symmetry (A) centre by an on-axis and an off-axis placement of a dopant cation, Sr²⁺+ or Ba²⁺, in the vicinity of the Ho³⁺ - F- pair. The three additional centres found in SrF₂:Ho³⁺ crystals are from similar Ca²⁺and Ba²⁺ substitutions in the SrF₂ lattice. Seven centres associated with n- charge compensation were observed in deuterated CaF₂:Ho³⁺ and SrF₂:Ho³⁺ crystals, with no C₄ᵥ symmetry centre being apparent. For the CsCdBr3:Ho³⁺ system, spectra of the principal dimer centre and three other minority centres are reported. Strong upconversion fluorescence was observed for the principal dimer centre, enabling crystal-field energy levels for 18 Ho³⁺ multiplets to be determined. Low symmetry crystal-field splittings and pair splittings were observed on some of the sharper transitions. Crystal-field analyses performed for all the C₄ᵥ and C₃ᵥ symmetry centres in CaF2:Ho³⁺, SrF2:Ho³⁺ and CsCdBr3:Ho³⁺ crystals are reported and the resulting crystal-field parameters discussed. Fluorescence lifetimes determined for the major Ho³⁺ centres are also presented. The high resolution and ODNMR results for the C₄ᵥ symmetry A and SB1 centres in SrF2:Ho³⁺ crystals confirm the centre symmetry assignments and the model configurations proposed on the basis of the polarisation ratio measurements. The superhyperfine ODNMR frequencies correlate well with the changes in the crystal-field parameters between the two centres.
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Zatari, Taha Mohammed. "High solids anaerobic digestion of the putrescible fraction of municipal solid waste." Thesis, University of Newcastle Upon Tyne, 1996. http://hdl.handle.net/10443/389.

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Anaerobic digestion is increasingly becoming essential for treating the organic fraction of municipal solid waste (MSW) according to the growing 'energy from waste' recycle concept. Over the last decade, efforts have been made to control the anaerobic digestion of the putrescible fraction of municipal solid waste in engineered reactors, rather than continuing with 'free' digestion in landfill sites. This way of increasing treatment efficiency can be achieved with significantly reduced retention time (days rather than years) and enables the recovery of valuable energy from waste without biogas emissions into the atmosphere, which cause adverse greenhouse effects. Three basic approaches have been explored for the anaerobic treatment of MSW: (a) conventional 'low solids' slurry digestion; (b) two-phase digestion; and (c) high solids 'dry and semi-dry' digestion. The advantages of high solids digestion processes include high loading rates, and high yields of biogas and methane. Anaerobic digestion at high solids content is also reported to reduce capital and operating costs through smaller reactor volume. Different reactor design configurations have been applied at full-scale and their performance evaluated. Commercial plants which use a high solids digestion process, recycle a portion of the digested solids residue in addition to the liquid from the digested residue. However, the exact recycling ratio and data concerning the recycling impact on the stability and performance of the digestion process, are not well documented in the literature. Also, it is recognised that mixing is important to enhance anaerobic digestion but little research has concentrated on the impact of mixing on continuous or semi-continuous high solids anaerobic digestion systems. The main aim of this research was to evaluate the potential methane production in the stabilisation of the putrescible fraction of MSW using two novel reactor designs. A vertical sequential reactor (VSR) was used to assess the effects of digested recycle ratio (DRR) and leachate recycling (LR) and a horizontal rotary reactor (I-IRR) was used to evaluate the impact of mixing on the digestion of the PFMSW. Experiments were conducted in both batch and semi-continuous mode using three 70 1 reactors, under mesophilic conditions (3 5°C) and high total solids content. Process performance was assessed using various waste parameters for solid waste and leachate treatment. Regarding solid waste treatment, VS removal, biogas and methane production and yields were the main parameters used for assessment, among several others. Accordingly, COD, VFA, pH, alkalinity, N1H3-N, TKN etc. have been some of the parameters used to monitor leachate quality. Furthermore, internal biological activity in the VSR was assessed using the observed VFA concentrations and degradation under different operational conditions (DRR and LR). Initially, batch experiments were carried out in order to evaluate the first start-up of high solids digestion. Furthermore, they provided seed digested residues for the subsequent semi-continuous studies, in addition to providing essential information regarding ultimate process efficiency in terms of methane yield and VS removal. Also, rapid start-up batch experiments were used to determine the required RT for semi-continuous studies. Optimum DRR and LR were determined with the use of the VSR semicontinuous process. A DRR of 0.5 was found to be optimum in terms of volumetric methane production, while LR2 (3.5 £ leachate recycle) provided a desirable economical option, because of its lower liquid requirements. I-IRR gave limited indicatory results expressing high treatment potential for high solids anaerobic digestion of the putrescible fraction of MSW. Finally, a mathematical model was developed for optimising the VSR operational conditions, utilising data produced under semi-continuous conditions.
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Kwetkus, Bernhard Andreas. "Contact electrification of solids /." [S.l.] : [s.n.], 1992. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=9788.

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Books on the topic "Solids"

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Seitz, Frederick. The modern theory of solids. New York: Dover Publications, 1987.

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Leonardi, Cesare. Solidi, 1983-1993 =: Solids, 1983-1993. S. Damaso, Modena: Logos, 1995.

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Riley, Peter D. Solids & liquids. North Mankato, MN: Smart Apple Media, 2008.

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Smoothey, Marion. Solids. New York: Marshall Cavendish, 1993.

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Ian, Graham. Solids. North Mankato, MN: Chrysalis Education, 2006.

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Hoffmann, Sara. Solids. Minneapolis: LernerClassroom, 2013.

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Smoothey, Marion. Solids. New York: Marshall Cavendish, 1993.

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Carr, Aaron. Solids. New York: AV² by Weigl, 2013.

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Harrison, Walter A. Electronic structure and the properties of solids: The physicsof the chemical bond. New York: Dover Publications, 1989.

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1931-, Laskar Amulya L., and Chandra Suresh 1938-, eds. Superionic solids and solid electrolytes: Recent trends. Boston: Academic Press, 1989.

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Book chapters on the topic "Solids"

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Askerov, Bahram M., and Sophia R. Figarova. "Solids." In Thermodynamics, Gibbs Method and Statistical Physics of Electron Gases, 175–212. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-03171-7_6.

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Manini, Nicola. "Solids." In Introduction to the Physics of Matter, 147–242. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-14382-8_5.

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de Oliveira, Mário J. "Solids." In Equilibrium Thermodynamics, 297–315. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36549-2_16.

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Watson, Keith L. "Solids." In Foundation Science for Engineers, 190–98. London: Macmillan Education UK, 1993. http://dx.doi.org/10.1007/978-1-349-12450-3_20.

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de Oliveira, Mário J. "Solids." In Equilibrium Thermodynamics, 315–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53207-2_16.

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Gooch, Jan W. "Solids." In Encyclopedic Dictionary of Polymers, 676. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_10860.

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Manini, Nicola. "Solids." In Introduction to the Physics of Matter, 149–244. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-57243-3_5.

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Allan, Neil, Elaine A. Moore, and Lesley E. Smart. "Solids." In Solid State Chemistry, 159–86. Fifth edition. | Boca Raton : CRC Press, [2021]: CRC Press, 2020. http://dx.doi.org/10.1201/9780429027284-4.

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Weigold, Erich, and Ian E. McCarthy. "Solids." In Electron Momentum Spectroscopy, 215–29. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4779-2_7.

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Watson, Keith L. "Solids." In Foundation Science for Engineers, 197–205. London: Macmillan Education UK, 1998. http://dx.doi.org/10.1007/978-1-349-14714-4_21.

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Conference papers on the topic "Solids"

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Phillips, Victor. "Smart Centrifuge for Solid Answers to Solids Control." In IADC/SPE Drilling Conference. Society of Petroleum Engineers, 1998. http://dx.doi.org/10.2118/39378-ms.

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Ramaswami, Krishnan, Yasushi Yamaguchi, and Fritz B. Prinz. "Spatial partitioning of solids for solid freeform fabrication." In the fourth ACM symposium. New York, New York, USA: ACM Press, 1997. http://dx.doi.org/10.1145/267734.267814.

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O’Hern, T. J., S. M. Trujillo, J. B. Oelfke, P. R. Tortora, and S. L. Ceccio. "Solids-Loading Measurements in a Gas-Solid Riser." In ASME 2004 Heat Transfer/Fluids Engineering Summer Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/ht-fed2004-56602.

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Gas-solid multiphase flows are commonly used in chemical processing, petroleum fluid catalytic cracking, and other industrial applications. The distribution of the solid phase in gas-solid flows (generally in the form of small particles) is seldom uniform, but more commonly involves clusters, streamers, and core-annular distributions, depending on the flow orientation and the overall gas and solid flowrates and their ratio. For this reason, tomographic techniques are of great interest for measurement of cross-sectional solids distributions in such flows. The cross-sectional profiles of solids loading can be integrated to yield a cross-sectionally averaged solids loading. Determination of this averaged solids loading is needed to understand the axial variations of solids loading and its sensitivity to flow parameters and to optimize performance. A common technique for determining volume-averaged solids loading in vertical flows like the riser section of a circulating fluidized bed (CFB) is by measurement of the time-averaged axial pressure gradients along the riser axis (differential pressure or ΔP method). Neglecting acceleration and wall friction, the axial momentum balance simplifies to equate the multiphase hydrostatic pressure term with the pressure gradient along the axis. Many authors (e.g., Louge and Chang, 1990) have pointed out the neglected terms in this approach and generally show that ΔP is applicable in the special cases of no solids-loading gradient (fully developed flow) or small solids flux. A more generally applicable technique for measuring solids loading in gas-solid flows is gamma tomography. A gamma tomography system using a 100-mCi Cs-137 source collimated into a fan beam and an array of scintillation detectors, has been developed and implemented for application to a cold-flow (non-reacting) CFB. The CFB has a 14-cm-ID 6-m tall riser, and is currently operated with a multiphase mixture of air and fluid catalytic cracking (FCC) catalyst particles. Typical operating conditions include mean superficial gas velocities up to 7.4 m/s and solids fluxes up to approximately 100 kg/m2·s. Quantitative comparison of gamma- and ΔP-determined solids loadings was made over a range of operating conditions (combination of superficial gas velocity and solids flux). Results indicate that the differences between gamma and ΔP-determined cross-sectionally averaged solids loading are most pronounced near the base of the riser, where solids concentration is highest and the mixture is accelerating. Higher in the riser, the agreement is better. Additionally, the difference is larger in cases of higher superficial gas velocity. In addition, several studies were performed to design an electrical-impedance tomography (EIT) system for a gas-solid flow to collect data suitable for validating computational models. A two-electrode bulk impedance system was studied experimentally. The required accuracy, spatial resolution and temporal resolution of an EIT system are addressed, and modeling and reconstruction are discussed. Bulk solid volume fractions measured by the two-electrode system and by gamma-densitometry tomography are in general agreement. Experiments with the two-electrode system also show that the Maxwell-Hewitt relation, used to convert the mixture impedance to solid volume fraction, must be applied carefully, paying attention to the identity of the dispersed and continuous phases. The design of a 16-electrode system is also described.
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Severino, Jose G., Luis Eduardo Gomez, Shoubo Wang, Ram S. Mohan, and Ovadia Shoham. "Mechanistic Modeling of Solids Separation in Solid/Liquid Hydrocyclones." In SPE Annual Technical Conference and Exhibition. Society of Petroleum Engineers, 2009. http://dx.doi.org/10.2118/124499-ms.

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Boissonnat, J. D. "Reconstruction of solids." In the first annual symposium. New York, New York, USA: ACM Press, 1985. http://dx.doi.org/10.1145/323233.323240.

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Pitt, Robert, and Shirley Clark. "Coarse Solids Management." In Water Resources and Environment History Sessions at Environmental and Water Reources Institute Annual Meeting 2004. Reston, VA: American Society of Civil Engineers, 2006. http://dx.doi.org/10.1061/9780784408728.006.

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Townsend, Joshua. "QMCPACK for Solids." In Proposed for presentation at the QMCPACK workshop in ,. US DOE, 2021. http://dx.doi.org/10.2172/1899258.

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Buehler, Blake, Pablo Moreno, Gustavious P. Williams, E. James Nelson, Oliver Obregon, Nicolas Gonzalez, and Nathan R. Swain. "Correlations between Total Solids, Total Suspended Solids, Total Volatile Suspended Solids, and Phosphate at Deer Creek Reservoir." In World Environmental And Water Resources Congress 2012. Reston, VA: American Society of Civil Engineers, 2012. http://dx.doi.org/10.1061/9780784412312.341.

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9

Machado, J. C., and P. F. Castilho. "Solids Control and Low-Solids: Important Binary to Drill Deep Wells." In SPE Latin America Petroleum Engineering Conference. Society of Petroleum Engineers, 1992. http://dx.doi.org/10.2118/23626-ms.

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10

Diaconescu, E. N., and V. F. Zegrean. "A Simple Flow Model for Amorphous Molecular Solids." In ASME 2008 9th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2008. http://dx.doi.org/10.1115/esda2008-59426.

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Abstract:
Theoretical and experimental investigations suggest that EHD oil films exhibit amorphous solid properties. Therefore, oil EHD traction properties may be found by the shear of corresponding molecular solids, such as amorphous paraffin. To check this possibility, the viscosity of solid paraffin under controlled pressure and temperature is measured on a computer assisted shear device. Experimental results indicate that some viscosity properties in amorphous solids do not match those found in liquids. AFM investigations show that solid paraffin structure is a mixture of clusters and simple molecules. A possible mechanism of flow in molecular amorphous solid was advanced which explains the observed discrepancies.
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Reports on the topic "Solids"

1

Murray, R. W. Solid state voltammetry and sensors in solids and gases. Office of Scientific and Technical Information (OSTI), April 1992. http://dx.doi.org/10.2172/5830050.

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2

Murray, R. (Solid state voltammetry and sensors in solids and gases). Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/5315509.

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3

Beaux, II, Miles Frank. Air-Buoyant Solids. Office of Scientific and Technical Information (OSTI), July 2017. http://dx.doi.org/10.2172/1367831.

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4

Holcomb, H. P. Tank C6A solids. Office of Scientific and Technical Information (OSTI), March 1988. http://dx.doi.org/10.2172/665917.

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5

Cooke, Gary A. Solid Phase Characterization of Solids Recovered from Failed Sluicer Arm. Office of Scientific and Technical Information (OSTI), March 2015. http://dx.doi.org/10.2172/1172386.

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6

Walker, D. D., and T. B. Edwards. Tetraphenylborate Solids Stability Tests. Office of Scientific and Technical Information (OSTI), December 1997. http://dx.doi.org/10.2172/301975.

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Hugo S. Caram and Natalie Foster. WET SOLIDS FLOW ENHANCEMENT. Office of Scientific and Technical Information (OSTI), July 1999. http://dx.doi.org/10.2172/780798.

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Caram, Hugo S., and Natalie Foster. WET SOLIDS FLOW ENHANCEMENT. Office of Scientific and Technical Information (OSTI), March 1997. http://dx.doi.org/10.2172/786382.

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Caram, Hugo S., and Natalie Foster. WET SOLIDS FLOW ENHANCEMENT. Office of Scientific and Technical Information (OSTI), March 1998. http://dx.doi.org/10.2172/786387.

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Caram, Hugo S., and Natalie Foster. WET SOLIDS FLOW ENHANCEMENT. Office of Scientific and Technical Information (OSTI), March 1999. http://dx.doi.org/10.2172/786388.

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