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Relevant bibliographies by topics / Inorganic polymers

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Academic literature on the topic 'Inorganic polymers'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 March 2023

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Journal articles on the topic "Inorganic polymers"

1

Chujo, Yoshiki, and Ryo Tamaki. "New Preparation Methods for Organic–Inorganic Polymer Hybrids." MRS Bulletin 26, no. 5 (May 2001): 389–92. http://dx.doi.org/10.1557/mrs2001.92.

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Nano-ordered composite materials consisting of organic polymers and inorganic compounds have been attracting attention for their use in creating high-performance or high-functionality polymeric materials. The term “polymer hybrid” describes blends of organic and inorganic components with molecular-level dispersions.

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Oleshkevich, Elena, Isabel Romero, Francesc Teixidor, and Clara Viñas. "All inorganic coordination polymers have been made possible with them-carboranylphosphinate ligand." Dalton Transactions 47, no. 41 (2018): 14785–98. http://dx.doi.org/10.1039/c8dt03264e.

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All inorganic coordination polymers (CPs) of Mn^II, Cd^IIand Zn^IIhave been achieved by using purely inorganicm-carboranylphosphinate ligands as a versatile building block bridging each of the two metal centres. The first described Cd^IIpolymer with phosphinate ligands is reported in this work.

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Juneja, H. D., Manisha Joshi, and N. T. KhatiI. "Synthesis and Structural Studies of Some Inorganic Polymers of Succinoyl Carboxymethyl Cellulose." E-Journal of Chemistry 8, no. 4 (2011): 1993–99. http://dx.doi.org/10.1155/2011/369492.

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The inorganic polymers containing transition metals such as Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) were synthesized by using succinoyl carboxymethyl cellulose (SCMC) in aqueous media. The newly synthesized polymers were characterized by elemental analysis, IR spectroscopy, TG analysis, UV reflectance spectra and magnetic moment. On the basis of these studies, the composition of the polymeric unit was found to be [M(II)L]n, [Mʼ(II)L.2H2O]n, {[Mˮ(II)L.2H2O]n H2O}, where M= Zn(II), Mʼ = Mn(II), Ni(II) and Cu(II) and Mˮ = Co(II), L = SCMC ligand. On the basis of instrumental techniques, it has been found that the [Zn(II)(SCMC)]n inorganic polymer has tetrahedral geometry, whereas {[Cu(II)(SCMC)].2H2O}n has square planar geometry and [Mn(II)(SCMC).2H2O]n, {[Co(II)(SCMC).2H2O)].H2O}n and [Ni(II) (SCMC).2H2O]n have octahedral geometry. The decomposition temperatures of the inorganic polymers have been determined by TGA. The TGA reveal that the Mn(II) polymer of SCMC is highly thermally stable than rest of the polymers and these polymers can be used as thermal resisting materials.

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PRASAD, P. N. "POLYMERS FOR PHOTONICS." Journal of Nonlinear Optical Physics & Materials 03, no. 04 (October 1994): 531–41. http://dx.doi.org/10.1142/s0218199194000316.

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Polymers have emerged as an important class of materials for applications in photon-ics. In this review, a brief background is presented on photonics and nonlinear optical processes, the latter providing many of the operational functions for the photonics technology. Nonlinear optical processes in polymeric materials are discussed along with the needed structural requirements. The three types of nonlinear polymeric systems discussed are: (i) χ(2) materials; (ii) χ(3) materials and (iii) photorefractive polymers. The photorefractive polymeric systems utilize the combined action of photoconductivity and nonlinear optical effect. New developments using sol-gel processed inorganic glass: polymer composites for nonlinear optics are discussed.

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KAJIWARA, Meisetsu. "Inorganic Polymers." Kobunshi 52, no. 2 (2003): 79. http://dx.doi.org/10.1295/kobunshi.52.79.

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Kuroda, Kazuyuki. "Inorganic polymers." Kobunshi 39, no. 10 (1990): 760–63. http://dx.doi.org/10.1295/kobunshi.39.760.

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Eaborn, Colin. "Inorganic polymers." Journal of Organometallic Chemistry 427, no. 2 (April 1992): C19. http://dx.doi.org/10.1016/0022-328x(92)83093-w.

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Khayal, Areeba. "A NOVEL ROUTE FOR THE FORMATION OF GAS SENSORS." International journal of multidisciplinary advanced scientific research and innovation 1, no. 6 (August 16, 2021): 96–108. http://dx.doi.org/10.53633/ijmasri.2021.1.6.04.

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The rapid development of conductive polymers shows great potential in temperature chemical gas detection as their electrical conductivity is often changed upon spotlight to oxidative or reductive gas molecules at room temperature. However, the relatively low conductivity and high affinity toward volatile organic compounds and water molecules always exhibit low sensitivity, poor stability and gas selectivity, which hinder their practical gas sensor applications. In addition, inorganic sensitive materials show totally different advantages in gas sensors like high sensitivity, fast response to low concentration analytes, high area and versatile surface chemistry, which could harmonize the conducting polymers in terms of the sensing individuality. It seems to be a good option to combine inorganic sensitive materials with polymers for gas detection for the synergistic effects which has attracted extensive interests in gas sensing applications. In this appraisal the recapitulation of recent development in polymer inorganic nanocomposites-based gas sensors. The roles of inorganic nanomaterials in improving the gas sensing performances of conducting polymers are introduced and therefore the progress of conducting polymer inorganic nanocomposites including metal oxides, metal, carbon (carbon nanotube, graphene) and ternary composites are obtainable. Finally, conclusion and perspective within the field of gas sensors incorporating conducting polymer inorganic nanocomposites are summarized. Keywords: Gas sensor, conducting polymer, polymer-inorganic nanocomposites; conducting organic polymers nanostructure, synergistic effect, polypyrrole (PPY), polyaniline (PANI).

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Ponou, Josiane, Tomohito Ide, Akiko Suzuki, Hideyuki Tsuji, Li Pang Wang, Gjergj Dodbiba, and Toyohisa Fujita. "Evaluation of the flocculation and de-flocculation performance and mechanism of polymer flocculants." Water Science and Technology 69, no. 6 (January 2, 2014): 1249–58. http://dx.doi.org/10.2166/wst.2014.004.

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Understanding the interaction mechanism between polymeric flocculants and solid particles in two oppositely charged solutions: bentonite and calcium fluoride, is of great practical and fundamental importance. In this work, inorganic flocculants based on aluminum(III) or iron(III); cationic, anionic and non-ionic organic flocculants were used. The solution pH, which highly influenced the flocculation performance of the system, has been used as a function of turbidity removal, sediment volume and velocity. Results show that the flocculation of inorganic polymers does not depend on the zeta potential but on the solution pH, contrary for cationic and anionic polymers. Non-ionic polymer was independent on both. By varying the final pH of the heterogeneous solution formed of flocs-liquid, it was found for inorganic polymers, the optimum condition of pH < 3 to separate inorganic flocculant particles from flocs. Inductively coupled plasma atomic emission spectrometer and X-ray fluorescence analysis proved the reversibility of flocculation process by indicating the concentration of flocculant representative atom (Al or Fe) in the flocs and in the emerging solutions when the flocculation was optimized and the reversibility was effective. As results, weak forces were suggested as responsible for inorganic polymers flocculation where electrostatic interaction and hydrogen bonds may enroll the mechanism of organic flocculants.

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Guglielmi, M., G. Brusatin, G. Facchin, and M. Gleria. "Hybrid materials based on the reaction of polyorganophosphazenes and SiO2 precursors." Journal of Materials Research 11, no. 8 (August 1996): 2029–34. http://dx.doi.org/10.1557/jmr.1996.0255.

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New molecular composite materials can be prepared based on an inorganic oxide network and an organic polymer. The polymeric component generally requires low process temperatures, due to the presence of the organic backbone or side groups. A sol-gel process therefore is suitable for synthesizing the inorganic component by dissolving soluble polymers into sol-gel precursor solutions in order to obtain ceramic and polymeric solid phases. In this work polyorganophosphazenes were used because they have many technologically interesting properties (chemical, optical, electrical, mechanical). The methods to obtain covalent bonds between polymer and inorganic network and to obtain homogeneous, transparent hybrid materials without phase separation were studied. It was possible to avoid phase separation by preparing phosphazenes containing free hydroxyl functions and by adequately choosing the experimental conditions.

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Dissertations / Theses on the topic "Inorganic polymers"

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HE, ZHOUYING. "ORGANIC/INORGANIC HYBRID COATINGS FOR ANTICORROSION." University of Akron / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=akron1437870016.

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Kyriazi, Eleni. "Inorganic/organic hybrid polymers." Thesis, University of Greenwich, 2005. http://gala.gre.ac.uk/6214/.

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The aims of this project were to synthesise and characterise a range of inorganic/organic hybrid polymers containing pendant vinyl groups and to study their uses as possible fire retardants. The work consisted of several parallel strands: the synthesis of organically modified silicas; the preparation of vinyl containing silsesquioxanes based on the hydrolysis of cyclohexyltrichlorosilane or propylmethacrylatepolysiloxane; the synthesis of latexes by co-polymerisation of either N-Isopropylacrylamide (NIPAM) or styrene with vinyltrimethoxysilane and the intercalation of styrene or NIPAM into montmorillonite. All samples were characterised using a range of instrumental techniques including infrared spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), X-ray diffraction (XRD), elemental analysis, thermal analysis, surface area analysis and electrokinetic analysis. Vinyl modified silicas having large surface areas (about 400m2g-1) were successfully obtained. On calcining at 540°C silicas having surface area in excess of 1000m2g-1 were formed. Both the original organically modified silica and a sample after calcining were incorporated into poly(methylmethacrylate) and these samples were compared with pure poly(methymethacrylate) in a cone calorimeter to study their thermal properties. No significant enhancement to the thermal stability of the polymers was observed when the silica was incorporated. Analysis of the co-polymer latexes were inconclusive, in the case of the products obtained from NIPAM but particles having a narrow size distribution were obtained using styrene. There was no apparent trend in the value of the zeta potential with composition. Analysis of the intercalation of monomers into clays and the synthesis of silsesquioxanes were inconclusive.

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Spinu, Maria. "Silicon-based organic and inorganic polymers." Diss., This resource online, 1990. http://scholar.lib.vt.edu/theses/available/etd-02052007-081236/.

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Chang, Kaiguo. "Synthesis and characterization of conducting polymer-inorganic composite materials /." View online ; access limited to URI, 2000. http://0-wwwlib.umi.com.helin.uri.edu/dissertations/dlnow/3108646.

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Abbas, Bassam. "Linear and nonlinear optical phenomena in thin sol-gel organic-inorganic films." Thesis, University of Reading, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298744.

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Lee, William K. "Solid-gel interactions in geopolymers." Connect to thesis, 2002. http://repository.unimelb.edu.au/10187/1071.

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This is partly because the requirements for such an ultimate material change with people’s perception about its properties as well as its environmental impact. Thus, the once-believed ultimate Portland cement binder is now becoming unacceptable for a number of reasons including poor durability as well as severe environmental impact during production. Thus, an improved mineral binder is required by modern society to serve the same purposes as the existing Portland cement binder, as well as to reduce the current environmental impact caused by Portland cement production.
Geopolymerisation is such a ‘green’ technology capable of turning both natural ‘virginal’ aluminosilicates and industrial aluminosilicate wastes, such as fly ash and blast furnace slag, into mechanically strong and chemically durable construction materials. However, the source materials for geopolymer synthesis are less reactive than Portland cement clinkers and the chemical compositions of these source materials can vary significantly. Consequently, product quality control is a major engineering challenge for the commercialisation of geopolymers.
This thesis is therefore devoted to the mechanistic understanding of the interfacial chemical interactions between a number of natural and industrial aluminosilicates and the various activating solutions, which govern the reactivity of the aluminosilicate source materials. The effects of activating solution alkalinity, soluble silicate dosage and anionic contamination on the reactivity of the aluminosilicate source materials to produce geopolymeric binders, as well as their bonding properties to natural siliceous aggregates for concrete making, are examined. In particular, a new set of novel ‘realistic’ reaction models has been developed for such purposes. These reaction models have been further utilised to develop a novel analytical procedure, which is capable of studying geopolymerisation on ‘real’ geopolymers in situ and in real time. This novel procedure is invaluable for the total understanding of geopolymerisation, which is in turn vital for effective geopolymer mix designs.

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Fan, Weizheng. "Development of Photoresponsive Polymers and Polymer/Inorganic Composite Materials Based on the Coumarin Chromophore." University of Akron / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=akron1366903513.

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Rahner, Nils. "Inorganic polymers (geopolymers) as potential bioactive materials : a thesis submitted to the Victoria University of Wellington in fulfilment of the requirements for the degree of Master of Science in Chemistry /." ResearchArchive@Victoria e-thesis, 2009. http://researcharchive.vuw.ac.nz/handle/10063/952.

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Myrex, Ronald Dustan. "Synthesis and characterization of phosphorus-containing inorganic polymers." Birmingham, Ala. : University of Alabama at Birmingham, 2007. https://www.mhsl.uab.edu/dt/2007r/myrex.pdf.

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Thesis (Ph. D.)--University of Alabama at Birmingham, 2007.
Additional advisors: Houston Boyd, Tracy Hamilton, Christopher Lawson, Charles Watkins. Description based on contents viewed Feb. 8, 2008; title from title screen. Includes bibliographical references.

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Köberle, Peter, and André Laschewsky. "Hybrid materials from organic polymers and inorganic salts." Universität Potsdam, 1994. http://opus.kobv.de/ubp/volltexte/2008/2688/.

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The prepaparation of amorphous, homogeneous blends of zwitterionic polymers and transition metal salts was investigated. Homogeneous miscibility was achieved in many cases up to equimolar amounts of salt, depending on the anion and cation chosen. Various analytical techniques point to a solid state solution of the inorganic ions in the polymer matrix.

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Books on the topic "Inorganic polymers"

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R, Allcock H., and West Robert 1928-, eds. Inorganic polymers. 2nd ed. New York: Oxford University Press, 2005.

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R, Allcock H., and West Robert 1928-, eds. Inorganic polymers. Englewood Cliffs, N.J: Prentice Hall, 1992.

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Müller, Werner E. G., Xiaohong Wang, and Heinz C. Schröder, eds. Biomedical Inorganic Polymers. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-41004-8.

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De, Jaeger Roger, and Gleria Mario, eds. Silicon-based inorganic polymers. New York: Nova Science Publishers, 2008.

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Archer, Ronald D. Inorganic and Organometallic Polymers. New York, USA: John Wiley & Sons, Inc., 2001. http://dx.doi.org/10.1002/0471224456.

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Zeldin, Martel, Kenneth J. Wynne, and Harry R. Allcock, eds. Inorganic and Organometallic Polymers. Washington, DC: American Chemical Society, 1988. http://dx.doi.org/10.1021/bk-1988-0360.

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Inorganic and organometallic polymers. New York: Wiley-VCH, 2001.

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Inorganic and organometallic polymers. Berlin: Springer, 2004.

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9

Wisian-Neilson, Patty, Harry R. Allcock, and Kenneth J. Wynne, eds. Inorganic and Organometallic Polymers II. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0572.

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Ropp, R. C. Inorganic polymeric glasses. Amsterdam: Elsevier, 1992.

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Book chapters on the topic "Inorganic polymers"

1

Gooch, Jan W. "Inorganic." In Encyclopedic Dictionary of Polymers, 390. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6345.

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Gooch, Jan W. "Inorganic Polymer." In Encyclopedic Dictionary of Polymers, 390. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6349.

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Naka, Kensuke. "Inorganic Polymers: Overview." In Encyclopedia of Polymeric Nanomaterials, 1–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-36199-9_121-1.

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Naka, Kensuke. "Inorganic Polymers: Overview." In Encyclopedia of Polymeric Nanomaterials, 995–1000. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_121.

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Gooch, Jan W. "Inorganic Coatings." In Encyclopedic Dictionary of Polymers, 390. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6346.

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Gooch, Jan W. "Inorganic Fibers." In Encyclopedic Dictionary of Polymers, 390. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6347.

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Gooch, Jan W. "Inorganic Pigments." In Encyclopedic Dictionary of Polymers, 390. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6348.

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Carraher, E. C. "Selected Polymers." In Inorganic Reactions and Methods, 201–2. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145326.ch109.

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Schmulbach, C. D. "Phosphonitrile Polymers." In Progress in Inorganic Chemistry, 275–379. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166055.ch5.

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Vohlídal, Jiří, and Muriel Hissler. "Metallo-Supramolecular Polymers." In Smart Inorganic Polymers, 141–62. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527819140.ch6.

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Conference papers on the topic "Inorganic polymers"

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Levenson, R., J. Liang, C. Rossier, M. Van Beylen, C. Samyn, F. Foll, Rousseau, and J. Zyss. "Stability-Efficiency Trade-Off in Non-Linear Optical Polymers." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.wd.6.

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Organic nonlinear optical materials have been the subject of increasing interest over the past decade[1]. Polymeric materials with highly polarizable molecules exhibit nonresonant NLO responses surpassing those obtained from traditional inorganic NLO materials, e.g. LiNbO3, KDP etc. Polymers offer the possibilities to optimize, by chemical synthesis, properties required for materials such as high mechanical and thermal stability. The dielectric constants of polymers ensure a very fast response-time for polymer devices [2], Compared to guest-host polymers, side chain polymers whereby NLO molecules are covalently attached lead to an increased density of nonlinear chromophores and may therefore exhibit higher nonlinear susceptibilities.

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Schmidt, H. "Inorganic-Organic Polymers as Materials for Optical Applications." In Optical Fabrication and Testing. Washington, D.C.: Optica Publishing Group, 1987. http://dx.doi.org/10.1364/oft.1987.waa3.

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The use of organic polymers for optical purposes requires special properties: The refractive index should be high or able to be adapted, light scattering should be extremely low, low thermal expansion and high surface hardness are advantageous. Temperature stability should be as high as 100 to 120 °C. Only a few organic polymeric materials have been used for optical purposes in the past e.g. PMMA, polycarbonate, polystyrene and CR 39 for eye glass lenses. Materials for contact lenses are a speciality, since additional requirements such as non-toxicity, oxygen permeability or surface hydrophilicity exist.

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Fujiwara, M., W. Mori, and K. Yamaguchi. "Molecular design of ferromagnetic and ferrimagnetic inorganic polymers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834721.

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Kippelen, Bernard, Sandalphon, Nasser Peyghambarian, Scott R. Lyon, Anne B. Padias, and Henry K. Hall. "Azo-dye-doped photorefractive polymers." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.thc.3.

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Since its recent discovery1, photorefractivity in polymers2-7 has attracted particular attention because photorefractive materials are versatile media for reversible optical storage applications and because organic materials like polymers have potential advantages over inorganic photorefractive crystals: low dielectric constant, ease of processing, and low cost. The capabilities of this new class of composites materials6 have rapidly reached a level comparable to those of some inorganic crystals and further improvement is expected since the magnitude of some intrinsic parameters such as the electro-optic coefficient for instance are not optimized yet. Here, we describe photorefractivity in azo-dye doped polymers. Azo dyes are molecules with strong second order nonlinear optical properties and are also known to undergo trans-cis photoisomerization8-9. The azo-dye-doped polymers presented here, can store two different types of erasable holograms originating from two different physical processes: photorefractivity and trans-cis photoisomerization. We show that the strong polarization nature of the isomerization process allows isolating exclusively the photorefractive effect by selecting the polarization of the reading beam. Moreover, we discuss the possible enhancement of the read-out photorefractive efficiency by photoisomerization-assisted poling of the sample.

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Kippelen, B., K. Meerholz, B. L. Volodin, Sandalphon, and N. Peyghambarian. "High Efficiency Photorefractive Polymers." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.wgg.2.

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The processibility and structural flexibility of photorefractive polymers give them an important technological potential and have driven intensive research efforts to improve the performance of this new class of PR materials. Since the first proof of principle of photorefractivity in a polymer [1], numerous PR polymeric materials have been synthesized by using different approaches [2], but significant performance improvement was obtained by using the photoconductive polymer poly(N-vinylcarbazole) (PVK) as the composite host and by doping it with nonlinear optical molecules referred to as chromophores [3,4]. In plasticized PVK-based polymer composites doped with the chromophore 2,5-dimethyl-4-(p-nitrophenylazo)anisole) (DMNPAA) [4], we recently demonstrated [5] that PR polymeric materials can exhibit light-induced refractive index modulation amplitudes as high as Δn = 7 × 10-3 at 1 W/cm2 writing intensity, and applied field of 90 V/µm. As shown in Fig. 1, such a high index modulation leads to complete diffraction and periodic energy transfer between the probe and diffracted beams in four-wave mixing (FWM) experiments and also, to net gain coefficients in excess of 200 cm-1 in two-beam coupling (TBC) experiments [5]. These results demonstrate that PR polymeric materials can reach performance levels that are competing with those of the best inorganic crystals, but with better processing capabilities.

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Baker, Gregory L., S. Etemad, and F. K ajzar. "Conjugated Polymers For Nonlinear Optics." In Advances in Nonlinear Polymers and Inorganic Crystals, Liquid Crystals, and Laser Media, edited by Solomon Musikant. SPIE, 1988. http://dx.doi.org/10.1117/12.941967.

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Tescione, F., G. G. Buonocore, M. Stanzione, M. Oliviero, and M. Lavorgna. "Controlling the release of active compounds from the inorganic carrier halloysite." In TIMES OF POLYMERS (TOP) AND COMPOSITES 2014: Proceedings of the 7th International Conference on Times of Polymers (TOP) and Composites. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4876874.

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Prasad, Paras N., Maciek E. Orczyk, Bogdan Swedek, Jaroslaw W. Zieba, Chanfeng Zhao, Chi-Kyun Park, Ryszard Burzynski, Yue Zhang, Saswati Ghosal, and Martin K. Casstevens. "Photorefractive processes in polymers and organic-inorganic glass composites." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by Gustaaf R. Moehlmann. SPIE, 1995. http://dx.doi.org/10.1117/12.222793.

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Feldmann, J., U. Lemmer, R. Hennig, A. Ochse, M. Hopmeier, E. O. Göbel, W. Guss, J. Pommerehne, R. Mahrt, and H. Bässler. "Polymers in Optical Micro cavities." In Quantum Optoelectronics. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/qo.1995.qthb4.

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The control of the emission properties of light-emitting devices is currently a subject of intense research in the field of inorganic as well as organic semiconductor physics [1]. The possibility to suppress or to enhance the spontaneous emission rate by using optical microcavities [2] is of particular interest, since this can lead to an enhanced light emission [3,4].

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Verdolotti, Letizia, Barbara Liguori, Ilaria Capasso, Domenico Caputo, Marino Lavorgna, and Salvatore Iannace. "Cellular morphology of organic-inorganic hybrid foams based on alkali alumino-silicate matrix." In TIMES OF POLYMERS (TOP) AND COMPOSITES 2014: Proceedings of the 7th International Conference on Times of Polymers (TOP) and Composites. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4876819.

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Reports on the topic "Inorganic polymers"

1

Sneddon, Larry G. Inorganic polymers and materials. Final report. Office of Scientific and Technical Information (OSTI), January 2001. http://dx.doi.org/10.2172/808136.

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Haddad, Timothy S., and Brent D. Viers. Organic Polymers Modified with Inorganic Polyhedra. Fort Belvoir, VA: Defense Technical Information Center, May 2002. http://dx.doi.org/10.21236/ada410052.

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Kunerth, D. C., and E. S. Peterson. Magnetic field processing of inorganic polymers. Office of Scientific and Technical Information (OSTI), May 1995. http://dx.doi.org/10.2172/105130.

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Phillips, S., R. Gonzales, K. Chaffee, T. Haddad, and G. Hoflund. Remarkable AO Resistance of POSS Inorganic/Organic Polymers. Fort Belvoir, VA: Defense Technical Information Center, January 2000. http://dx.doi.org/10.21236/ada397900.

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Phillips, Shawn H., Rene I. Gonzalez, Rusty L. Blanski, Brent D. Viers, and Gar B. Hoflund. Hybrid Inorganic/Organic Reactive Polymers for Severe Environment Protection. Fort Belvoir, VA: Defense Technical Information Center, February 2002. http://dx.doi.org/10.21236/ada410034.

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Allcock, Harry L. Inorganic-Organic Polymers and Their Role in Materials Science. Fort Belvoir, VA: Defense Technical Information Center, May 1994. http://dx.doi.org/10.21236/ada279715.

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Matyjaszewski, Krzysztof. Preparation of Inorganic and Organometallic Polymers with Controlled Structures. Fort Belvoir, VA: Defense Technical Information Center, May 1991. http://dx.doi.org/10.21236/ada235359.

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Allcock, Harry R. Reactions of Inorganic High Polymers as a Route to Tailored Solids. Fort Belvoir, VA: Defense Technical Information Center, February 1989. http://dx.doi.org/10.21236/ada204602.

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Matyjaszewski, Krzysztof. Catalysts and Initiators as Instruments Controlling Structure of Polymers with Inorganic Backbone. Fort Belvoir, VA: Defense Technical Information Center, May 1991. http://dx.doi.org/10.21236/ada235350.

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Allcock, Harry R. Strained Inorganic Heterocyclic Compounds and their Conversion to Macrocycles and High Polymers. Fort Belvoir, VA: Defense Technical Information Center, October 1991. http://dx.doi.org/10.21236/ada241414.

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