Gotowe bibliografie tematyczne / Sol-gel

Spis treści

  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji
  6. Raporty organizacyjne

Gotowa bibliografia na temat „Sol-gel”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 26 października 2024

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Artykuły w czasopismach na temat "Sol-gel"

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Shkuropatenko, V. A. "Sol-gel synthesis of NZP phosphates". Functional materials 23, nr 1 (15.03.2016): 92–97. http://dx.doi.org/10.15407/fm23.01.092.

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MACKENZIE, John D. "Sol-Gel Optics". Journal of the Ceramic Society of Japan 101, nr 1169 (1993): 1–10. http://dx.doi.org/10.2109/jcersj.101.1.

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NAKAZUMI, Hiroyuki. "Sol-Gel Process". Journal of the Japan Society of Colour Material 68, nr 4 (1995): 245–51. http://dx.doi.org/10.4011/shikizai1937.68.245.

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Livage, J. "Sol-gel processes". Current Opinion in Solid State and Materials Science 2, nr 2 (kwiecień 1997): 132–38. http://dx.doi.org/10.1016/s1359-0286(97)80057-5.

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Livage, J., i C. Sanchez. "Sol-gel chemistry". Journal of Non-Crystalline Solids 145 (styczeń 1992): 11–19. http://dx.doi.org/10.1016/s0022-3093(05)80422-3.

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Moszner, Norbert, Alexandros Gianasmidis, Simone Klapdohr, Urs Karl Fischer i Volker Rheinberger. "Sol–gel materials". Dental Materials 24, nr 6 (czerwiec 2008): 851–56. http://dx.doi.org/10.1016/j.dental.2007.10.004.

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LIVAGE, J. "Sol-gel ionics". Solid State Ionics 50, nr 3-4 (luty 1992): 307–13. http://dx.doi.org/10.1016/0167-2738(92)90234-g.

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Schmidt, H. "Sol-Gel-Processing". Physik Journal 45, nr 10 (październik 1989): 418–19. http://dx.doi.org/10.1002/phbl.19890451014.

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Schubert, Ulrich. "Sol-Gel-Chemie". Chemie in unserer Zeit 52, nr 1 (8.09.2017): 18–25. http://dx.doi.org/10.1002/ciuz.201700792.

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Reuter, Hans. "Sol-gel processes". Advanced Materials 3, nr 5 (maj 1991): 258–59. http://dx.doi.org/10.1002/adma.19910030510.

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Rozprawy doktorskie na temat "Sol-gel"

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Yang, Quanzu. "Composite sol-gel ceramics". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape8/PQDD_0019/NQ46453.pdf.

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Zheng, Lei. "Cobaltferrite-bariumtitanate sol-gel biferroics". College Park, Md. : University of Maryland, 2006. http://hdl.handle.net/1903/3648.

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Thesis (M.S.) -- University of Maryland, College Park, 2006.
Thesis research directed by: Dept. of Material Science and Engineering. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
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Gardener, Martin. "Studies in sol-gel chemistry". Thesis, Nottingham Trent University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341276.

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Borislav, Simendić. "Niskotemperaturno procesiranje sol-gel mulita". Phd thesis, Univerzitet u Novom Sadu, Tehnološki fakultet Novi Sad, 2003. https://www.cris.uns.ac.rs/record.jsf?recordId=71471&source=NDLTD&language=en.

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Apstrakt je obrađen tehnologijama za optičko prepoznavanje teksta (OCR).Mehanizam nastanka mulita zavisi od načina doziranja polaznih oblika reaktanata kao što su alumina i silika. Dobijanje mulita sol-gel postupkom je u velikoj meri poboljšano u odnosu na klasično procesiranje zbog mogućnosti homogenog mešanja AI2O3 i SiO2 komponenti i kontrole dodataka. Sol-gel metod omogućuje pripremu vrlo homogenih i reaktivnih gelova koji mogu da sinteruju na nižim temperaturama pri čemu se može postići vrlo fina mikrostruktura. U ovom radu koji se odnosio na procesiranje mulita sol-gel postupkom, hipoteza je bila da se na samom početku procesiranja aluminijumovi joni iz alkoholnog rastvora Al-soli uključuju u polimernu gel strukturu koju formira silika. Svrha ovog rada, je proučavanje uticaja procesnih promenjivih, dodatka fluornog jona i “seedinga” na temperaturu nastanka sol-gel mulita pri čemu se očekuje što je moguće niža tempertura nastanka mulita (niža od 9800C). Polimerni sol je dobijen u prvom slučaju mešanjem TEOS-a i aluminijum nitrata nanohidrata koji je prethodno rastvoren u etil alkoholu. U drugom slučaju, u polimerni sol je dodavan fluorni jon u koncentraciji 2 do 5 % mas. u odnosu na očekivani prinos mulita i u trećem slučaju je dodavana različita količina mulitnih klica (2-4 % mas.). Eksperimantalno je potvrđeno da procesne promenljive; pH, temperatura geliranja i R odnos imaju, veliki uticaj na brzinu geliranja i na nastanak mulita. U slučaju dodavanja fluornog jona, potvrdena je hipoteza da fluorni jona na različite načine utiče na mehanizam nastanka mulita, pri čemu u prvom slučaju prisustvo fluornog jona obezbeduje mesta u oblastima razdvajanja granica faza nakon geliranja koja utiču na proces nukleacije. Ova mesta slično procesu kristalizacije stakla, omogućuju lakšu nukleaciju mulita prilikom njegove transformacije iz gela. Mesta na granici razdvanja faza postaju mesta na kojima se uspostavlja proces heterogene nukleacije što je jedan od mogućih načina za snižavanje temperature nastanka mulita. Pored ovoga, dodavanje fluornog jona je doprinelo promeni mulitnih gel struktura, pri čemu je promena brzine hidrolize silike imala za posledicu promenu sadržaja vezane vode u toku geliranja što se takođe značajno odražavalo na temperaturu nastanka mulita. Eksperimentalni rezultati termički obradenih gelova su pokazali, da dodavanje lluornog jona u polimerni mulitni sol stvara uslove za snižavanje temperature obrazovanja mulita sve do 8900C. U ovom radu je takođe pokazano da mulitne čestice, kao nukleanti pri “seeding" procesiranju, doprinose nastanku mulitnog gela koji nakon termičke obrade na 10000C pokazuje veoma finu mikrostrukturu.
Abstract was processed by technology for Optical character recognition (OCR).The mechanism of mullite formation depends upon the method of combining the alumina and silica containing reactants. Mullite can be obtained through the sol-gel process and can be greatly improved by the control of some reaction conditions particulaiiy by homogeneous mixing of Al2O3 and SiO2, and controlling of the additions. Sol-gel method allow preparation of very homogenous and reactive gels which can be sintering at low temperature and consequently submicronic microstructure can be reached. In this study of the mullite formation by sol-gel method, the hypothesis was that aluminium ions from alcoholic solulion of its salts incorporate to polymeric silica gel structure. The aim of this work was the investigation of the effect processing variables, fluorine addition and “seeding”on the temperature of sol-gel mullite formation and to obtain as lower temperature of mullite formation as possible (smaller than 980°C). Polymeric sols, were prepared by the mixing of TEOS and aluminum nitrate nanohydrate dissolved in absolute ethyl alcohol and by adding fluorine ions in the second case from 2 wt.% to 5 wt.% and by different content of mullite seeded (2- 4 wt. %). Experimentally is determined that the processing variables as pH, gelling temperature and R ratio have high influence on the gelling rate and mullite formation. The hypothesis in the case of fluorine addition was that addition of fluorine ions could have different effects on the mechanism of mullite formation; the first it makes the sites at boundary of phase separation regions after gelling which influence at the process of the nucleation. These sites will act as a place for easy mullite nucleation, similar to process of the glass crystallization. The boundaries of the phase separation are the sites for heterogeneous nucleation which is one of the condition for lowering the temperature of mullite formation. Besides, fluorine addition could change the mullite gel structure (by changing the rate of hydrolyses of silica and it could change the content of bonded water during gelling), which should be very important for the temperature of mullite formation, too. The experimental results of heat treated gels showed that the addition of fluorine ion does decrease the temperature of mullite formation (in respect to classical sol-gel mullite processing) up to 8900C. As a nucleant in this study the mullite powder by “seeding” process contribute to muillite gel formation that after heat treatment up to 10000C showed very fine microstructure.
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Pohl, Annika. "Sol−Gel Synthesis of CMR Manganites". Doctoral thesis, Uppsala University, Department of Materials Chemistry, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3970.

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The development of more advanced materials forms the basis of technological progress. One group of fascinating compounds with many potential applications in spintronic devices are the mixed-valence perovskite manganites. These have attracted considerable interest during the last decade through their very large magnetoresistance near the Curie Temperature. Although the properties of a material determinie any application, the development of reliable and flexible synthesis methods is crucial, as is the understanding of these methods. Knowledge of how different materials are formed is also of general importance in tailoring new materials. The aim of this project has therefore been not only to develop a new synthesis route, but also to understand the mechanisms involved.

This thesis describes the synthesis and characterization of a novel manganese alkoxide and its use in sol–gel processing of magnetoresistive perovskite manganites. In searching for a soluble manganese alkoxide for sol–gel processing, we found that the methoxy-ethoxide, [Mn19O12(moe)14(moeH)10]·moeH, has a high solubility in appropriate organic solvents. Being 1.65 nm across, it is one of the largest alkoxides reported; it is also of interest because of its (for oxo-alkoxides) rare planar structure. After mixing with La, Nd, Ca, Sr, and Ba methoxy-ethoxides, [Mn19O12(moe)14(moeH)10]·moeH was used in the first purely alkoxide based sol–gel processing of perovskites manganites. The phase evolution on heating xerogel powders to 1000°C was studied, and thin films were prepared by spin-coating.

It was found that the easily oxidised Mn-alkoxide facilitates the formation of high oxygen-excess modifications of the perovskites. The reactive precursor system yields fully hydrolysed gels almost without organic residues, but the gel absorbs CO2 from the air, leading to carbonate formation. The carbonate decomposition is the limiting step in oxide formation. Transport measurements of La0.67Ca0.33MnO3 films on LaAlO3 substrate show that all-alkoxide sol–gel derived films can compete with PLD films in terms of quality of epitaxy and transport. The somewhat different behaviour of the sol–gel derived films compared to PLD films is attributed to differences in morphology and oxygen stoichiometry.

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Barreau, Stephanie. "Biosensing with sol-gel-immobilised proteins". Thesis, Loughborough University, 1999. https://dspace.lboro.ac.uk/2134/27275.

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Low temperature-processed, porous sol-gel glasses represent a new class of materials for the immobilisation of biomolecules. If used to entrap biological recognition elements, these transparent and chemically inert glasses offer a new approach in the development of optical biosensors.
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Noureddine, Achraf. "Approches Click en Chimie Sol-Gel". Thesis, Montpellier, Ecole nationale supérieure de chimie, 2014. http://www.theses.fr/2014ENCM0005/document.

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Nous visons dans ce travail de thèse à développer une méthodologie de fonctionnalisation par chimie click des silices hybrides synthétisées par voie sol-gel. La réaction click de cycloaddition azoture-alcyne catalysée au cuivre (CuAAC) offre une tolérance exceptionnelle pour les fonctions organiques en plus de conversions très élevées. Dans cette optique, nous avons mis en œuvre en premier lieu des matériaux clickables à base d'organosilice pure (organosilice à mésoporosité périodique (PMO) et silsesquioxanes pontés (BS)) qui ont permis une conversion quasi-quantitative de greffage par CuAAC. Nous avons ensuite utilisé cette particularité pour contrôler les propriétés de surface des BS en modifiant leur caractère hydrophile/lipophile. Dans le second axe de travail, nous nous sommes intéressés à l'apport de la chimie click pour la préparation de nanoparticules mésoporeuses de silice multifonctionnelles, dites mécanisées, pour des systèmes à délivrance contrôlée de principes actifs
The present work aims to develop a trustful methodology of functionalization for hybrid silica materials made by the sol-gel process using the copper-catalyzed alkyne-azide cycloaddition (CuAAC)Click reaction. This transformation can be highly useful in materials science thanks to its high conversions and the excellent functional group tolerance. In this prospect, we have synthesized fully clickable bridged silisesquioxanes and periodic mesoporous organosilica that show high extents of click grafting. CuAAC was then used for tailoring the surface of bridged silsesquioxane and fine-tuning the hydrophilic/lipophilic balance. Finally, the click reaction was used as an efficient way to obtain multiply functionalized mesoporous silica nanoparticles in order to make nanomachines for controlled delivery of cargo molecules
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Stani´c, Vesha. "Sol-gel processing of metal sulfides". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq21641.pdf.

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Chisham, Jason E. (Jason Edward). "Sol-gel materials for integrated optics". Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=23992.

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The sol-gel process is a low temperature solution route to amorphous and crystalline materials. Organic modification of the precursors allows the formation of organic-inorganic composite materials. We use the sol-gel process to produce an organically-modified ceramic for integrated optical applications. Photosensitive organic components allow the fabrication of passive integrated optical devices by photolithography. We demonstrate the fabrication and characterization of channel waveguides, waveguide devices and gratings in this material. Active devices based on the emission of erbium at 1.55 $ mu$m are under much investigation because of their potential use in telecommunications. Luminescence quenching is a major problem as an Er$ sp{3+}$ ion in its excited state transfers its energy to a nearby vibrational mode of its environment and decays non-radiatively to the ground state. Encapsulation of the ion into a coordination sphere to shield the ion from its surroundings may lead to reduced quenching. We synthesize several erbium tetrakis $ beta$-diketone complexes and dope them into different solvent environments and sol-gel hosts to probe guest-host interactions in the excited state.
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Bellatone, Maria. "Sol-gel derived antimicrobial bioactive glass". Thesis, Imperial College London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394943.

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Książki na temat "Sol-gel"

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Klein, Lisa C., red. Sol-Gel Optics. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3.

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Guglielmi, Massimo, Guido Kickelbick i Alessandro Martucci, red. Sol-Gel Nanocomposites. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1209-4.

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Levy, David, i Marcos Zayat, red. The Sol-Gel Handbook. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527670819.

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W, Scherer George, red. Sol-gel science: The physics and chemistry of sol-gel processing. Boston: Academic Press, 1990.

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Attia, Yosry A., red. Sol-Gel Processing and Applications. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2570-7.

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Pierre, Alain C. Introduction to Sol-Gel Processing. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5659-6.

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Innocenzi, Plinio. The Sol to Gel Transition. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39718-4.

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Pierre, Alain C. Introduction to Sol-Gel Processing. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38144-8.

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Innocenzi, Plinio. The Sol-to-Gel Transition. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-20030-5.

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Pierre, Alain C. Introduction to sol-gel processing. Boston: Kluwer Academic Publishers, 1998.

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Części książek na temat "Sol-gel"

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Johnson, D. W. "Sol-Gel". W Inorganic Reactions and Methods, 9–10. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145333.ch5.

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Rabinovich, Eliezer M. "Sol Gel Processing — General Principles". W Sol-Gel Optics, 1–37. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_1.

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Klein, Lisa C. "Nanocomposite Fabrication for Transparent Windows". W Sol-Gel Optics, 215–32. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_10.

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Ganguli, Dibyendu. "Single Layer and Multilayer Colored Coatings on Glass". W Sol-Gel Optics, 233–54. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_11.

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Sayer, M., i G. Yi. "Sol Gel Processing of Ferroelectric Films". W Sol-Gel Optics, 255–77. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_12.

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Shahriari, M. R., i J. Y. Ding. "Doped Sol-Gel Films for Fiber Optic Chemical Sensors". W Sol-Gel Optics, 279–302. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_13.

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Zink, Jeffrey I., i Bruce Dunn. "Sol-Gel Encapsulated Molecules: Optical Probes and Optical Properties". W Sol-Gel Optics, 303–28. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_14.

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Nogami, Masayuki. "Semiconductor-Doped Sol-Gel Optics". W Sol-Gel Optics, 329–44. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_15.

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López, Tessy, i Ricardo Gómez. "Catalyst Doped Sol-Gel Materials". W Sol-Gel Optics, 345–71. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_16.

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Che, Tessie M., Mark A. Banash, Paul R. Soskey i Paul B. Dorain. "Gel Derived Gradient Index Optics — Aspects of Leaching and Diffusion". W Sol-Gel Optics, 373–90. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2750-3_17.

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Streszczenia konferencji na temat "Sol-gel"

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Davis, S. R., A. Wilson i J. D. Wright. "Flammable gas sensors based on sol-gel materials". W IEE Colloquium on Sol-Gel Materials for Device Applications. IEE, 1998. http://dx.doi.org/10.1049/ic:19980581.

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Phillips, Nicholas J. "Sol-gel technology". W SIRA - DL tentative, redaktor Lionel R. Baker. SPIE, 1992. http://dx.doi.org/10.1117/12.57755.

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Newport, A., J. Silver i A. Vecht. "Synthesis of luminescent sol gel materials for active electronic devices". W IEE Colloquium on Sol-Gel Materials for Device Applications. IEE, 1998. http://dx.doi.org/10.1049/ic:19980577.

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Seddon, A. B. "Sol-gel derived organic-inorganic hybrid materials for photonic applications". W IEE Colloquium on Sol-Gel Materials for Device Applications. IEE, 1998. http://dx.doi.org/10.1049/ic:19980582.

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Sale, F. R. "The citrate-gel processing of electronic and magnetic ceramics". W IEE Colloquium on Sol-Gel Materials for Device Applications. IEE, 1998. http://dx.doi.org/10.1049/ic:19980580.

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Perry, C. "Chemical considerations in the formulation of sol-gel materials for device applications". W IEE Colloquium on Sol-Gel Materials for Device Applications. IEE, 1998. http://dx.doi.org/10.1049/ic:19980578.

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Hodgson, S. N. B., L. Weng i S. M. Tracey. "Sol-gel processing of tellurium oxide thin films for optical data storage application". W IEE Colloquium on Sol-Gel Materials for Device Applications. IEE, 1998. http://dx.doi.org/10.1049/ic:19980579.

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Zhang, Q., R. W. Whatmore, M. E. Vickers i Z. Huang. "Structural studies on sols for PZT thin films". W IEE Colloquium on Sol-Gel Materials for Device Applications. IEE, 1998. http://dx.doi.org/10.1049/ic:19980583.

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Darracq, B., D. Riehl, M. Canva, Y. Levy i A. Brun. "Photorefractive Sol-Gel Films". W Proceedings of European Meeting on Lasers and Electro-Optics. IEEE, 1996. http://dx.doi.org/10.1109/cleoe.1996.562357.

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Ulatowska-Jarża, A., U. Bindig, H. Podbielska, I. Hołowacz, I. Gersonde, J. Beuthan, G. Müller i H. J. Eichler. "Photoactive sol-gel biocoatings". W SPIE Proceedings, redaktorzy Katarzyna Kolacz i Jacek Sochacki. SPIE, 2006. http://dx.doi.org/10.1117/12.676078.

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Raporty organizacyjne na temat "Sol-gel"

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Caverly, Spencer. LCO Synthesis by Sol-Gel Method. Office of Scientific and Technical Information (OSTI), październik 2024. http://dx.doi.org/10.2172/2463015.

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Young, Sandra K. Overview of Sol-Gel Science and Technology. Fort Belvoir, VA: Defense Technical Information Center, styczeń 2002. http://dx.doi.org/10.21236/ada398036.

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Debsikdar, J., E. Samsel, C. Sellers, K. Telschow i D. Miley. Superconducting film fabrication by the sol-gel process. Office of Scientific and Technical Information (OSTI), wrzesień 1989. http://dx.doi.org/10.2172/5651016.

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Ramamurthi, S. Molecular growth pathways in silica sol-gel polymerization. Office of Scientific and Technical Information (OSTI), styczeń 1989. http://dx.doi.org/10.2172/6236739.

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Simpson, Randall L., William Hubble, Bradley Stevenson, Alexander Gash, Joe Satcher i Patricia Metcalf. Safe and Environmentally Acceptable Sol-Gel-Derived Pyrophoric Pyrotechnics. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2004. http://dx.doi.org/10.21236/ada438451.

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Benicewicz, Brian C., Glenn A. Eisman, S. K. Kumar i S. G. Greenbaum. Sol-Gel Based Polybenzimidazole Membranes for Hydrogen Pumping Devices. Office of Scientific and Technical Information (OSTI), luty 2014. http://dx.doi.org/10.2172/1121336.

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Kueper, T. W. Sol-gel derived ceramic electrolyte films on porous substrates. Office of Scientific and Technical Information (OSTI), maj 1992. http://dx.doi.org/10.2172/5011926.

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Simspon, R., J. Satcher i A. Gash. Safe and Environmentally Acceptable Sol-gel Derived Pyrophoric Pyrotechnics. Office of Scientific and Technical Information (OSTI), czerwiec 2004. http://dx.doi.org/10.2172/15014310.

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Knobbe, Edward T. Sol-Gel Derived Surface Treatments for Aircraft Aluminum Alloys. Fort Belvoir, VA: Defense Technical Information Center, marzec 2002. http://dx.doi.org/10.21236/ada405721.

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Kueper, Timothy Walter. Sol-gel derived ceramic electrolyte films on porous substrates. Office of Scientific and Technical Information (OSTI), maj 1992. http://dx.doi.org/10.2172/10159001.

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