Relevant bibliographies by topics / Solid state chemistry

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Solid state chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 29 July 2024

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Journal articles on the topic "Solid state chemistry"

1

DiSalvo, F. J. "Solid state chemistry." Solid State Communications 102, no. 2-3 (April 1997): 79–85. http://dx.doi.org/10.1016/s0038-1098(96)00713-2.

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Kauzlarich, Susan M. "Special Issue: Advances in Zintl Phases." Materials 12, no. 16 (August 11, 2019): 2554. http://dx.doi.org/10.3390/ma12162554.

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Zintl phases have garnered a great deal of attention for many applications. The term “Zintl phase” recognizes the contributions of the German chemist Eduard Zintl to the field of solid-state chemistry. While Zintl phases were initially defined as a subgroup of intermetallic phases where cations and anions or polyanions in complex intermetallic structures are valence satisfied, the foundational idea of electron counting to understand complex solid-state structures has provided insight into bonding and a bridge between solid-state and molecular chemists. This Special Issue, “Advances in Zintl Phases”, provides a collage of research in the area, from solution to solid-state chemistry.
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TAKAMURA, Hitoshi. "Solid State Chemistry Division." Denki Kagaku 89, no. 4 (December 5, 2021): 395. http://dx.doi.org/10.5796/denkikagaku.21-ot0047.

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Byrn, S. R., R. R. Pfeiffer, G. Stephenson, D. J. W. Grant, and W. B. Gleason. "Solid-State Pharmaceutical Chemistry." Chemistry of Materials 6, no. 8 (August 1994): 1148–58. http://dx.doi.org/10.1021/cm00044a013.

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Whittingham, M. Stanley. "Solid state chemistry. Techniques." Solid State Ionics 34, no. 3 (May 1989): 213. http://dx.doi.org/10.1016/0167-2738(89)90045-3.

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Wold, Aaron. "Basic solid state chemistry." Journal of Solid State Chemistry 82, no. 1 (September 1989): 179. http://dx.doi.org/10.1016/0022-4596(89)90241-7.

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Catlow, C. R. A. "Computational solid state chemistry." Computational Materials Science 2, no. 1 (January 1994): 6–18. http://dx.doi.org/10.1016/0927-0256(94)90042-6.

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Green, Malcolm L. H., Jingui Qin, and Dermot O'Hare. "Organometallic solid state chemistry." Journal of Organometallic Chemistry 358, no. 1-3 (December 1988): 375–88. http://dx.doi.org/10.1016/0022-328x(88)87091-8.

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Lorenzelli, V. "Basic solid state chemistry." Materials Chemistry and Physics 21, no. 3 (March 1989): 320. http://dx.doi.org/10.1016/0254-0584(89)90128-4.

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Schedler, U., J. Bendig, and L. Dähne. "Solid State Chemistry of Polymethines." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 264, no. 1 (May 1995): 11–21. http://dx.doi.org/10.1080/10587259508037297.

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Dissertations / Theses on the topic "Solid state chemistry"

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Qin, J. "Studies in organometallic solid state chemistry." Thesis, University of Oxford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379942.

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Brown, Craig. "Solid state chemistry of selected fullerenes." Thesis, University of Sussex, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.264552.

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Peacock, Heather Margaret. "Solid state oxide chemistry of ruthenium." Thesis, University of Aberdeen, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.257552.

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The oxygen stoichiometry of RuO2+atop -x was investigated by thermogravimetric and isopiestic techniques, in the temperature range 200-800oC. RuO2+atop -x could be made hyperstoichiometric to a maximum of RuO2.014 at 500oC and hypostoichiometric to a maximum of RuO1.9808 at 600oC. Above 800oC loss of ruthenium as the volatile species RuO3(g) and RuO4(g) prevented any reasonable determination of oxygen stoichiometry. Solid solutions were prepared in the Ru-V-O, Ru-Nb-O, Ru-W-O and Ru-Mo-O systems by solid state reaction. Complete solid solution was observed in the Ru-V-O system. Unit cell parameters were determined by X-ray powder diffraction for a range of compositions in the Ru-V-O system. Large deviations from the linearity predicted by Vegard's law were found for both a and c, e.g. at 5 wt.% vanadium a = 4.489, c = 3.089 and at 75 wt.% vanadium a = 4.592, c = 2.873. Conductivity of polycrystalline pressed pellets of RuO2:VO2 solid solutions was measured using a four point probe technique. All small vanadium concentrations conductivity increased with percent dopant i.e. resistivity decreased from 8.5 k Ω cm at 2 wt.% vanadium to 4.5 k Ω cm at 5 wt.% vanadium. Solid solutions containing 25-85 wt.% vanadium were found to be semiconducting and increasing amounts of vanadium in this range produced no significant change in resistivity. Solid solutions containing 95 wt.% vanadium showed a transition, at -13oC, from metallic to semiconducting behaviour as the temperature was lowered. In the Ru-Nb-O, Ru-W-O and Ru-Mo-O systems only 5 wt.% dopant could be successfully incorporated into the RuO2 lattice. On the basis of the Ru-V-O system however these materials are considered to be potentially good conductors. Resistor inks dilute in ruthenium could prove economically viable. The high vanadium containing materials may have potential as temperature sensitive electronic switching devices. The temperature programmed reduction of an RuO2:VO2 solid solution containing 25 wt.% vanadium showed that the onset of reduction occurred at a much higher temperature (234oC) than for RuO2 itself (63oC). This suggests that vanadium containing solid solutions of RuO2 are more resistant to reduction than RuO2 itself, a much sought after property in the production of thick film resistors.
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Wilson, Graeme. "Solid-state chemistry of zirconium dioxide." Thesis, University of Aberdeen, 1987. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU009973.

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A systematic literature search on the system Na2O-ZrO2-SiO2 is presented which reveals inconsistencies on the number and identity of the ternary phases. New X-ray diffraction data are presented for Na2ZrSiO5, Na2ZrSi2O7 and Na2ZrSi4O11; these data are substantiated by good agreement with data calculated from single-crystal work. The unit-cell parameters were redetermined. The compounds Na2ZrSi4O11 and Na4Zr2Si10O31 have now been successfully synthesised by solid state reaction, although the latter could not be prepared phase-pure; these phases had previously only been synthesised hydrothermally. The subsolidus compatibility relations at 1000oC have been reassessed, taking into account the two phases mentioned above, which have not featured in any previously published phase diagram. The addition of dopants, such as calcia, magnesia or yttria, as the oxide, carbonate etc., into solid solution with zirconia are known to stabilise the cubic phase to room temperature. A comparative trial is reported of the physical properties of these powders produced using either organic or inorganic gel-processing routes; the organic route consistently provided powders with greater thermal stability and surface area, which should lead to a more sinterable product, therefore this method was extended to include lanthanide oxide dopants. The incorporation of these dopants has been previously reported, but long sintering times at elevated temperatures were necessary; the organic precursor route described above successfully produced cubic zirconia more rapidly and at much reduced temperatures. The gelation tendencies of the lanthanide dopants are discussed. The binary system ZrO2-SnO2 was investigated at various temperatures; at 1000oC one metastable phase, zirconium stannate, which was observed previously but was poorly characterised, has been studied by X-ray diffraction techniques; new unit-cell parameters and X-ray diffraction data are presented; these data have been substantiated by agreement with calculated data. This phase has now been shown, by various techniques, to exsolve to two distinct phases with average compositions 90ZrO210SnO2 and 82SnO218ZrO2. The monoclinic zirconia solid-solution has been proven by the influence of this inclusion of tin oxide on the physical properties of pure monoclinic zirconia. A discussion of the crystallography of zirconium titanate, which is isostructural with zirconium stannate, is also reported. The extent of solid solubility of tin oxide in zirconium titanate has been determined at 1000, 1350, 1500 and 1550oC; the compositions in this single-phase region are known as zirconium tin titanates and are used as microwave dielectric resonators. A large metastable region of ZrO2-TiO2 solid solution was noted at 1000oC which is similar to data previously published. At 1350oC, the extent of solid solution in the ternary region was also as previously published, but a vast increase in solid-solubility was noted at higher temperatures. A comparison of the dielectric properties of pellets produced by mixed oxide sintering and gel-processing is reported.
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Vitorica, Inigo. "Solid state supramolecular chemistry : gas-solid reactions and intermolecular interactions." Thesis, University of Sheffield, 2012. http://etheses.whiterose.ac.uk/3926/.

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Gallon, Daniel. "Structure-property relationships in solid state chemistry." Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270616.

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Khamar, Dikshitkumar. "Solid state chemistry of hydrate forming compounds." Thesis, Liverpool John Moores University, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555688.

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Polymorphism presents complex issues for the pharmaceutical industry from processing, regulatory, patenting and stability perspectives. It can be further challenging to control the same form throughout processing and development when it has the capacity to form a hydrate. Incorporation of water into the crystal lattice contributes to significant differences in solubility, stability and bioavailability of the active pharmaceutical ingredient (API). During processing and formulating steps, water is used in many procedures such as, recrystallisation, wet granulation, aqueous coating lyophilisation etc. This can trigger anhydrous to hydrate conversion and could be detrimental for bioavailability and stability of the product. The factors responsible for this type of transition such as, role of solvent, activity of solvent, thermodynamic stability of different forms, equilibrium conditions, processing induced transformations are investigated. Theophylline, a channel hydrate, is chosen as a model compound which exhibits both polymorphs and solvates. The value of water activity at which the theophylline monohydrate is thermodynamically stable form was investigated using solubility, cooling crystallisation and slurry experiments and found to be aw 2: 0.70 at 25 QC. Full characterisation of the solid state chemistry of theophylline has resulted in the discovery of a new, previously unreported, anhydrous form of theophylline, called Form IV. Using solubility, crystallisation, slurrying and thermal experiments, Form IV was found to be thermodynamically more stable than the currently known stable form, Form H. The crystal structure of Form IV and Form I was determined by single crystal :X-Ray diffraction technique. The crystal structures for Form IV and Form I are deposited in Cambridge Structural Database (CSD) with reference code BAPLOT03 and BAPLOT04 respectively. The experimentally observed stability behaviour was correlated with the structural features of solid forms and also with the energy calculations. The kinetic ally stable Form H serves as the intermediate for polymorphic and hydrate-anhydrate transformations as the catemer motif observed in Form II can easily propagate by forming a strong and directional hydrogen bonds. In contrast, the dimer of theophylline molecules as observed in Form IV needs the presence of solvent to link through other dimers only by weak interactions. This results in the generation of Form IV only via solvent mediated transformations. Solid state chemistry of hydrate forming compounds Theophylline has also been used here as a model compound to study eo crystallisation with various saturated, dicarboxylic acids. A new, eo crystal of theophylline with adipic acid was generated and using thermal methods and PXRD, the stoichiometry (1 :2, adipic acid: theophylline) is confirmed. The complex hydration-dehydration behaviour of theophylline was investigated. The samples subjected to different pharmaceutical processing conditions for hydration-dehydration, generated various .intermediate phases suggesting multiple dehydration mechanisms and the potential of phase transformations during processing of such kind of hydrate forming compounds. The sensitivity of thermal methods over other bulk methods such as PXRD, in detecting a small amount of phase impurity, has been highlighted.
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Brown, Michael Ewart. "Reactions in the solid state." Link to this resource, 2005. http://eprints.ru.ac.za/252/.

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Thesis (D.Sc. (Chemistry)) - Rhodes University, 2006.
[Appendix]. Dedication - Acknowledgements - Curriculum vitae - Biographical notes - Publication list - Introduction to my research - Commentary-books - Commentary-research papers - Conclusions.
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Brown, Michael Ewart. "Reactions in the solid state." Thesis, Rhodes University, 2006. http://hdl.handle.net/10962/d1015762.

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I have chosen the title for this thesis, "Reactions in the Solid State", for two reasons: Firstly, it is broad enough to cover all of my areas of research, which have been: • Effects of irradiation on solids (PhD topic) • Silver refining (while at the Chamber of Mines) • Kinetics of decomposition of solids (with Dr A.K. Galwey and various others) • Techniques of thermal analysis • Pyrotechnic delay systems (with support from AECI Explosives) • Thermal and photostability of drugs (with Prof B.D. Glass) and, secondly, it was the title of the very successful book co-authored by Drs Andrew Galwey, David Dollimore and me. A large part of my research has been involved in the writing and editing of books, so these are covered in a separate commentary, while commentary on the more than 100 papers to which I have contributed forms the main part of this compilation. It is hoped that the electronic format will enable ready access of to all aspects of my research, including electronic versions of the original papers. The reader will need a copy of Adobe Acrobat Reader to access these.
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Drummond-Brydson, Richard. "Electron energy loss spectroscopy in solid-state chemistry." Thesis, University of Cambridge, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.237906.

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Books on the topic "Solid state chemistry"

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K, Cheetham A., and Day Peter 1938-, eds. Solid state chemistry: Techniques. Oxford: Clarendon, 1988.

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Moore, Elaine A., and Lesley E. Smart. Solid State Chemistry. Fifth edition. | Boca Raton : CRC Press, [2021]: CRC Press, 2020. http://dx.doi.org/10.1201/9780429027284.

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Wold, Aaron, and Kirby Dwight. Solid State Chemistry. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1476-9.

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Smart, Lesley, and Elaine Moore. Solid State Chemistry. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-6830-2.

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Chakrabarty, D. K. Solid state chemistry. New Delhi: New age international publishers, 2005.

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1928-, Ardon Michael, ed. Solid state chemistry. Berlin: Springer-Verlag, 1987.

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K, Cheetham A., and Day P, eds. Solid state chemistry: Techniques. Oxford [Oxfordshire]: Clarendon Press, 1987.

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R, Desiraju G., ed. Organic solid state chemistry. Amsterdam: Elsevier, 1987.

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K, Cheetham A., and Day P, eds. Solid state chemistry: Compounds. Oxford [England]: Clarendon Press, 1992.

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R, West Anthony, ed. Basic solid state chemistry. Chichester [West Sussex]: Wiley, 1988.

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Book chapters on the topic "Solid state chemistry"

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Fahlman, Bradley D. "Solid-State Chemistry." In Materials Chemistry, 13–156. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-0693-4_2.

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Fahlman, Bradley D. "Solid-State Chemistry." In Materials Chemistry, 13–85. Dordrecht: Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6120-2_2.

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Fahlman, Bradley D. "Solid-State Chemistry." In Materials Chemistry, 23–169. Dordrecht: Springer Netherlands, 2018. http://dx.doi.org/10.1007/978-94-024-1255-0_2.

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Fahlman, Bradley D. "Solid-State Chemistry." In Materials Chemistry, 31–189. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-18784-1_2.

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Hickey, Anthony J., and Stefano Giovagnoli. "Solid-State Chemistry." In AAPS Introductions in the Pharmaceutical Sciences, 5–10. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-91220-2_2.

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Catlow, C. R. A., R. M. Barrer, and I. S. Kerr. "Solid state chemistry." In 100 Years of Physical Chemistry, 339–50. Cambridge: Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847550002-00339.

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Ehrenfreund, Pascale, and Helen Fraser. "Ice Chemistry in Space." In Solid State Astrochemistry, 317–56. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0062-8_10.

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Jha, Ashok Kumar. "Solid-State Reactions." In Solid-State Chemistry, 1–18. New York: Apple Academic Press, 2023. http://dx.doi.org/10.1201/9781003328629-1.

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van der Put, Paul J. "Structural Solid State Chemistry." In The Inorganic Chemistry of Materials, 111–65. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-0095-1_4.

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Koltzenburg, Sebastian, Michael Maskos, and Oskar Nuyken. "Polymers in Solid State." In Polymer Chemistry, 93–103. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49279-6_4.

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Conference papers on the topic "Solid state chemistry"

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Zharikov, E. V. "CHROMIUM-DOPED GARNET HOSTS: CRYSTAL CHEMISTRY DEVELOPMENT AND PROPERTIES." In Advanced Solid State Lasers. Washington, D.C.: OSA, 1986. http://dx.doi.org/10.1364/assl.1986.tha1.

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Patil, Supriya Veer, Ashwini Kshirsagar, Deepali D. Andhare, Supriya R. Patade, Govind D. Kulkarni, and K. M. Jadhav. "Synthesis of nanocrystalline nickel ferrite through soft chemistry method: A green chemistry approach using ginger extract." In DAE SOLID STATE PHYSICS SYMPOSIUM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0017071.

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Toner, Brandy M., Brandi Cron, Colleen Hoffman, Sarah L. Nicholas, and Brandy Stewart. "Solid-State Chemistry of Near-Field Hydrothermal Particles." In Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.2610.

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Kushwaha, Ajay, Vijay Singh, M. Aslam, Alka B. Garg, R. Mittal, and R. Mukhopadhyay. "Energy Efficient and Size Tunable Synthesis of ‘Colloidal’ Zinc Oxide Nanoparticles by Simple Beaker Chemistry." In SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3605899.

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Singh, Kulwinder, Manjeet Kumar, Paviter Singh, Gurpreet Kaur, Bikramjeet Singh, Anup Thakur, Ju-Hyung Yun, and Akshay Kumar. "NiO nanostructures: Effect of iron doping on structural, defect chemistry and spectroscopic properties." In DAE SOLID STATE PHYSICS SYMPOSIUM 2018. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5112960.

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Petricevic, V. "Novel Cr4+- Based Tunable Solid-State Lasers." In Recent Advances in the Uses of Light in Physics, Chemistry, Engineering, and Medicine. SPIE, 1992. http://dx.doi.org/10.1117/12.2322284.

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Ghosh, Swapan K. "Chemistry of molecules to physics of materials: A unified view through density window at different length scales." In SOLID STATE PHYSICS: Proceedings of the 56th DAE Solid State Physics Symposium 2011. AIP, 2012. http://dx.doi.org/10.1063/1.4709865.

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Chuang, T. J. "Laser Induced Gas-Surface Chemistry and Photoetching of Solids." In 1986 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1986. http://dx.doi.org/10.7567/ssdm.1986.a-4-1.

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Kolb, Vera M. "Solventless and solid-state reactions as applied to the meteoritic chemistry." In SPIE Optical Engineering + Applications, edited by Richard B. Hoover, Gilbert V. Levin, Alexei Y. Rozanov, and Paul C. W. Davies. SPIE, 2010. http://dx.doi.org/10.1117/12.858621.

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MADAR, ROLAND. "CRYSTAL CHEMISTRY OF METAL SILICIDES." In Proceedings of the 16th Course of the International School of Solid State Physics. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812792136_0001.

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Reports on the topic "Solid state chemistry"

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Bernhard, W. Solid state radiation chemistry of the DNA backbone. Office of Scientific and Technical Information (OSTI), September 1989. http://dx.doi.org/10.2172/5430309.

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Processing water-chemistry data, Gulf Coast aquifer systems, south-central United States; with summary of dissolved-solids concentrations and water types. US Geological Survey, 1986. http://dx.doi.org/10.3133/wri864186.

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