Bibliografías temáticas / Organosilica

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Literatura académica sobre el tema "Organosilica"

Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 10 de febrero de 2022

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Artículos de revistas sobre el tema "Organosilica"

Mohd, Hanafi Ani, Maziati Akmal Mohd Hatta y Raihan Othman. "Effect of Al Ions on Adsorption Efficiency of Mesoporous Organosilica for Water Treatment". Advanced Materials Research 415-417 (diciembre de 2011): 2024–31. http://dx.doi.org/10.4028/www.scientific.net/amr.415-417.2024.

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Porous organosilica is a promising material to be applied in water treatment due to high adsorption capacity of contaminants. Sol-gel method was used to fabricate mesoporous organosilioca from triblock copolymers, poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) as the template and tetraethylorthosilicate as silicate source. The organosilica is doped with Al powder and Al2SO3 in order to evaluate the effect of ions on their adsorption capacity. It was demonstrated that the adsorption capacity is proportional to Al concentration, and inversely proportional to porosity. Metallic compound doped in organosilica enhances the remediation process and optimize the water treatment process. Moreover, impregnation the samples into cellulosic sponge improves the adsorption efficiency by 25%.

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Asefa, Tewodros y Zhimin Tao. "Mesoporous silica and organosilica materials — Review of their synthesis and organic functionalization". Canadian Journal of Chemistry 90, n.º 12 (diciembre de 2012): 1015–31. http://dx.doi.org/10.1139/v2012-094.

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Mesoporous silica and organosilica materials are a class of nanostructured materials that have porous structures with tunable nanometer pores, large surface areas, high pore volumes, and, in some cases, well-ordered mesostructures. Furthermore, in the case of mesoporous organosilicas, the materials possess various types of organic functional groups. This review highlights the different synthetic methods developed for mesoporous silica and organosilica nanomaterials. The review also discusses the various synthetic strategies used to functionalize the surfaces of mesoporous silica materials and produce highly functionalized mesoporous materials. Rational design and synthetic methods developed to place judiciously chosen one or more than one type of functional group(s) on the surfaces of mesoporous silica materials and generate monofunctional and multifunctional mesoporous silica materials are also introduced. These organic functionalization methods have made possible the synthesis of organically functionalized mesoporous silicas and mesoporous organosilicas with various interesting properties and many potential applications in different areas, ranging from catalysis to drug delivery and biosensing.

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Nakamura, Michihiro. "Biomedical applications of organosilica nanoparticles toward theranostics". Nanotechnology Reviews 1, n.º 6 (1 de diciembre de 2012): 469–91. http://dx.doi.org/10.1515/ntrev-2012-0005.

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AbstractNanoparticles for biomedical applications have several advantages as multifunctional agents. Among various types of nanoparticles for biomedical applications, silica nanoparticles have characteristic positioning due to their inherent property. The recent development of silica nanoparticles is creating a new trend in nanomedicine. A novel type of silica nanoparticle, organosilica nanoparticle, is both structurally and functionally different from the common (inorgano)silica nanoparticle. The organosilica nanoparticles are inherent organic-inorganic hybrid nanomaterials. The interior and exterior functionalities of organosilica nanoparticles are useful for their multifunctionalization. Biomedical applications of organosilica nanoparticles are leading to a wide range of nanomedical fields such as basic biomedical investigations and clinical applications. Multifunctionalizations peculiar to organosilica nanoparticles enable the creation of novel imaging systems and therapeutic applications. In this review, I will introduce differences between (inorgano)silica nanoparticles and organosilica nanoparticles, and then focus on biomedical applications of organosilica nanoparticles toward theranostics.

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Niu, Dechao, Yongsheng Li y Jianlin Shi. "Silica/organosilica cross-linked block copolymer micelles: a versatile theranostic platform". Chemical Society Reviews 46, n.º 3 (2017): 569–85. http://dx.doi.org/10.1039/c6cs00495d.

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Silica/organosilica cross-linked block copolymer micelles are a novel class of hybrid materials that combine the advantages of amphiphilic block copolymers and silica/organosilica cross-linking agents into one unit. This Tutorial Review summarizes the recent progress in the design, synthesis and biomedical applications of various silica/organosilica cross-linked block copolymer micelles.

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Poscher, Vanessa y Yolanda Salinas. "Trends in Degradable Mesoporous Organosilica-Based Nanomaterials for Controlling Drug Delivery: A Mini Review". Materials 13, n.º 17 (19 de agosto de 2020): 3668. http://dx.doi.org/10.3390/ma13173668.

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The last few years of enhancing the design of hybrid mesoporous organosilica nanoparticleshas allowed their degradation under specific pathologic conditions, which finally is showing a lightin their potential use as drug delivery systems towards clinical trials. Nevertheless, the issueof controlling the degradation on-demand at cellular level still remains a major challenge, even if ithas lately been addressed through the incorporation of degradable organo-bridged alkoxysilanesinto the silica framework. On this basis, this mini review covers some of the most recent examplesof dierent degradable organosilica nanomaterials with potential application in nanomedicine,from degradable non-porous to mesoporous organosilica nanoparticles (MONs), functionalized withresponsive molecular gates, and also the very promising degradable periodic mesoporous organosilicamaterials (PMOs) only consisting of organosilica bridges.

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Zebardasti, Ali, Mohammad Dekamin y Esmail Doustkhah. "The Isocyanurate-Carbamate-Bridged Hybrid Mesoporous Organosilica: An Exceptional Anchor for Pd Nanoparticles and a Unique Catalyst for Nitroaromatics Reduction". Catalysts 11, n.º 5 (12 de mayo de 2021): 621. http://dx.doi.org/10.3390/catal11050621.

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Hybridisation of mesoporous organosilicas (MO) to reinforce the surface capability in adsorption and stabilisation of noble metal nanoparticles is of great attention in generating/supporting noble metal within their matrices and transforming them into efficient heterogeneous catalysts. Here, we used a unique hybrid of organic-inorganic mesoporous silica in which pore profile pattern was similar to the well-known mesoporous silica, SBA-15 for catalysis. This hybrid mesoporous organosilica was further engaged as a support in the synthesis and stabilisation of Pd nanoparticles on its surface, and then, the obtained Pd-supported MO was employed as a heterogeneous green catalyst in the conversion of aqueous p-nitrophenol (PNP) to p-aminophenol (PAP) at room temperature with efficient recyclability.

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Ren y Tsuru. "Organosilica-Based Membranes in Gas and Liquid-Phase Separation". Membranes 9, n.º 9 (22 de agosto de 2019): 107. http://dx.doi.org/10.3390/membranes9090107.

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Organosilica membranes are a type of novel materials derived from organoalkoxysilane precursors. These membranes have tunable networks, functional properties and excellent hydrothermal stability that allow them to maintain high levels of separation performance for extend periods of time in either a gas-phase with steam or a liquid-phase under high temperature. These attributes make them outperform pure silica membranes. In this review, types of precursors, preparation method, and synthesis factors for the construction of organosilica membranes are covered. The effects that these factors exert on characteristics and performance of these membranes are also discussed. The incorporation of metals, alkoxysilanes, or other functional materials into organosilica membranes is an effective and simple way to improve their hydrothermal stability and achieve preferable chemical properties. These hybrid organosilica membranes have demonstrated effective performance in gas and liquid-phase separation.

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Jaroniec, Mietek. "Organosilica the conciliator". Nature 442, n.º 7103 (agosto de 2006): 638–40. http://dx.doi.org/10.1038/442638a.

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Knezevic, Nikola Z., Chiara Mauriello Jimenez, Martin Albino, Aleksandar Vukadinovic, Ana Mrakovic, Erzsebet Illes, Djordje Janackovic, Jean-Olivier Durand, Claudio Sangregorio y Davide Peddis. "Synthesis and Characterization of Core-Shell Magnetic Mesoporous Silica and Organosilica Nanostructures". MRS Advances 2, n.º 19-20 (2017): 1037–45. http://dx.doi.org/10.1557/adv.2017.69.

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ABSTRACTInitial results en route toward construction of complex magnetic core-shell silica and organosilica nanotheranostics are presented. Magnetite nanoparticles are synthesized by three different methods and embedded within mesoporous silica and organosilica frameworks by different surfactant-templated procedures to produce three types of core-shell nanoparticles. Magnetite nanoparticles (15 nm in diameter) are embedded within mesoporous silica nanoparticles to produce cell-like material with predominantly one magnetite nuclei-resembling core per nanoparticle, with final particle diameter of ca. 150 nm, specific surface area of 573 m2/g and hexagonally structured tubular pores (2.6 nm predominant diameter), extended throughout the volume of nanoparticles. Two forms of spherical core-shell nanoparticles composed of magnetite cores embedded within mesoporous organosilica shells are also obtained by employing ethylene and ethane bridged organobisalkoxysilane precursors. The obtained nanomaterials are characterized by high surface area (978 and 820 m2/g), tubular pore morphology (2 and 2.8 nm predominant pore diameters), different diameters (386 and 100-200 nm), in case of ethylene- and ethane-composed organosilica shells, respectively. Different degree of agglomeration of magnetite nanoparticles was also observed in the obtained materials, and in the case of utilization of surfactant-pre-stabilized magnetite nanoparticles for the syntheses, their uniform and non-agglomerated distribution within the shells was noted.

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Poscher, Vanessa, George S. Pappas, Oliver Brüggemann, Ian Teasdale y Yolanda Salinas. "Hybrid Porous Microparticles Based on a Single Organosilica Cyclophosphazene Precursor". International Journal of Molecular Sciences 21, n.º 22 (13 de noviembre de 2020): 8552. http://dx.doi.org/10.3390/ijms21228552.

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Porous organosilica microparticles consisting of silane-derived cyclophosphazene bridges were synthesized by a surfactant-mediated sol-gel process. Starting from the substitution of hexachlorocyclotriphosphazene with allylamine, two different precursors were obtained by anchoring three or six alkoxysilane units, via a thiol-ene photoaddition reaction. In both cases, spherical, microparticles (size average of ca. 1000 nm) with large pores were obtained, confirmed by both, scanning and transmission electron microscopy. Particles synthesized using the partially functionalized precursor containing free vinyl groups were further functionalized with a thiol-containing molecule. While most other reported mesoporous organosilica particles are essentially hybrids with tetraethyl orthosilicate (TEOS), a unique feature of these particles is that structural control is achieved by exclusively using organosilane precursors. This allows an increase in the proportion of the co-components and could springboard these novel phosphorus-containing organosilica microparticles for different areas of technology.

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Tesis sobre el tema "Organosilica"

Mun, Ellina A. "Functionalised organosilica nanoparticles : synthesis, mucoadhesion and diffusion". Thesis, University of Reading, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.659018.

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Organosilica nanoparticles, due to their versatile properties, attract considerable attention for pharmaceutical applications. The first chapter of this thesis gives an introduction to organosilica materials and traditional methods of their synthesis, provides a literature review on functionalisaUon of silica nanoparticles, in particular PEGylation, and describes recently investigated routes of their application in pharmaceutical science. This is followed by a brief description of methods and techniques used in the current study for synthesis and characterisation of organosilica nanoparticles. Chapter 3 represents a novel size-controlled method of synthesis of thiolated and PEGylated organosilica nanoparticles from 3-mercaptopropyltrimethoxysilane (MPTS) using various organic solvents as media. The mechanism of the nanoparticle formation is proposed, the dependence of nanoparticles size on solvent's dielectric constant is determined, and other factors affecting the nanoparticle size are investigated. Thiol-groups on the surface of organosilica nanoparticles are available for a direct conjugation. Therefore, their surfaces were funcUonalised with two types of fluorescent dyes and PEG maleimide of two molecular weights (750and 5000 Oa). Additionally, polymer- and surfactant-templated mechanisms of MPTS nanoparticle formaUon are reported. The synthesis chapter is followed by studying the properties of thiolated and PEGylated organosilica nanoparticles. Mucoadhesive properties of silica nanoparticles were investigated using a newlyintroduced in vitro method assessing their retention ability on the urinary bladder by the means of fluorescence microscopy. The main factors affecting mucoadhesive properties of MPTS nanoparticles were revealed and thiolated nanoparticles were demonstrated to be promising mucoadhesive materials for intravesical drug delivery. PEGylated nanoparticles were found to be less mucoadhesive which led to the hypothesis of providing better permeation by PEGylation. This was considered in the subsequent chapter (chapter 5), studying the barrier functions of the cornea using thiolated and PEGylated nanoparticles. The "whole eye" in vitro method combined with the fluorescence microscopy demonstrated a good permeation of the latter through de-epithelialised ocular tissue into the stroma. This revealed the interaction of nanoparticles with the corneal surface to be a more impcrtant factor than the particle size, determining their permeation ability. As most organs of the human body are covered with biological hydrogels, the ability of silica nanoparticles to permeate through biological tissues has risen an interest in studying their capability to diffuse through such gels. Therefore, the diffusion of thiolated and PEGylated nanoparticles in different polymer solutions, which were selected as prototypes of biological hydrogels, was studied using NanoSight tracking analysis with fluorescent detection. The main factors affecting the diffusion of organosilica nanoparticles were revealed, and it was demonstrated that the presence of strong attractive interactions between the nanoparticles and macromolecules present in solutions can hamper the diffusion. This was followed by studying biocompatible properties of organosilica nanoparticles using an alternative to traditional methods, a slug mucosal irritation test, revealing their non-irritant nature. Finally, the general results of the current study are summarised and discussed in the last chapter of the thesis, proposing plans for the future work and expansion of the investigations on organosilica nanoparticles presented so far.

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Jahns, Mandy [Verfasser]. "Nanoporöse Organosilica-Materialien für biomedizinische Anwendungen / Mandy Jahns". Hannover : Gottfried Wilhelm Leibniz Universität Hannover, 2019. http://d-nb.info/1190283433/34.

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Terpstra, Andrea Susanne. "Chiral nematic mesoporous organosilica materials templated with cellulose nanocrystals". Thesis, University of British Columbia, 2017. http://hdl.handle.net/2429/64160.

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Voß, Rebecca. "Mesoporous organosilica materials with amine functions : surface characteristics and chirality". Phd thesis, Universität Potsdam, 2005. http://opus.kobv.de/ubp/volltexte/2005/528/.

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In this work mesoporous organisilica materials are synthesized through the silica sol-gel process. For this a new class of precursors which are also surfactant are synthesized and self-assembled. This leads to a high surface area functionality which is analysized with copper (II) and water adsorption.
Im Rahmen dieser Arbeit werden mesoporöse Amin-funktionalisierte Organo-Silikate durch den Silika Sol-Gel Prozess hergestellt. Dabei werden neue Alkoxysilyl-Precursoren synthetisiert und condensiert die die gewünschte Funktion auf die Oberfläche dirigieren. Herstellt werden primäre, secundäre und chirale Amine. Die Oberflächenfunktionalität wird mit Kupfer (II) und Wasser Adsorption analysiert.

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Gehring, Julia Johanna [Verfasser]. "Mesoporous organosilica nanoparticles as antibacterial coating materials / Julia Johanna Gehring". Konstanz : Bibliothek der Universität Konstanz, 2016. http://d-nb.info/1118316541/34.

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Voss, Rebecca. "Mesoporous organosilica materials with amine functions surface characteristics and chirality /". [S.l. : s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=975976362.

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De, Witt Joanna Christine. "Switching the reflection in chiral nematic mesoporous silica and organosilica films". Thesis, University of British Columbia, 2012. http://hdl.handle.net/2429/43781.

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Simon, Tamás [Verfasser] y Michael [Akademischer Betreuer] Fröba. "Periodisch Mesoporöse Organosilica - Mit speziellen Morphologien - / Tamás Simon ; Betreuer: Michael Fröba". Hamburg : Staats- und Universitätsbibliothek Hamburg, 2019. http://d-nb.info/1186891874/34.

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Ide, Andreas Hans Peter. "Self-Structuring of functionalized micro- and mesoporous organosilicas using boron-silane-precursors". Phd thesis, Universität Potsdam, 2008. http://opus.kobv.de/ubp/volltexte/2008/2371/.

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The structuring of porous silica materials at the nanometer scale and their surface functionalization are important issues of current materials research. Many innovations in chromatography, catalysis and electronic devices benefit from this knowledge. The work at hand is dedicated to the targeted design of functional organosilica materials. In this context a new precursor concept based on boron-silanes is presented. These precursors combine the properties of a structure directing group and a silica source by covalent borane linkage. Formation of the precursor is easily realized by a sequential two-step hydroboration, firstly on bis(triethoxysilyl)ethene, and secondly on an unsaturated structure directing moiety such as alkenes or polymers. The so prepared precursors self-organize when hydrolysis of their inorganic moiety takes place via an aggregation of their organic side chains into hydrophobic domains. In this way, the additional use of a surfactant as a template is not necessary. Chemical cleavage of these moieties (e.g. by ammonolysis or oxidative saponification) yields an organosilica where all functionalities are exclusively located at the pore wall and therefore accessible. The accessibility of the functionalities is a vital point for applications and is not necessarily granted for common silica functionalization approaches. Further advantages of the boron-silane concept are the possibility to introduce a variety of surface functionalities by heterolytic cleavage of the boron linker and the control of the pore morphology. For that purpose the covalent linkage of different alkyl groups and polymers was studied. Another aspect is the access to chiral boron silane precursors yielding functionalized mesoporous organosilica with chiral functionalities exclusively located at the pore walls after condensation and removal of the structure directing moiety. These materials possess great potential for applications documented by preliminary investigations on chiral resolution of a racemic mixture by HPLC and asymmetric catalysis. In the course of this work valuable insights into the targeted structuring and surface functionalization of organosilicas were gained. A promising outlook for further investigations is the extension of this concept by altering the structure directing moieties of the precursor. That way the morphology of the final organosilica might be controlled by for example mesogens. Furthermore, the use of the boron linker enables the introduction of multiple functionalities into organosilicas, making the obtained material unique in its performance.
Die Nanostrukturierung von funktionalisierten porösen Materialien auf Silikatbasis steht im Brennpunkt der aktuellen Forschung. Anwendungen wie Chromatographie, Katalyse oder die Herstellung elektronischer Bauteile profitieren von den Erkenntnissen, die auf diesem Gebiet gewonnen werden. Die vorliegende Arbeit soll einen Beitrag zur gezielten Herstellung dieser Funktions-materialien leisten. Hierfür wurde ein neues Precursor-Konzept auf der Basis von Borsilanen vorgestellt. Diese Precursoren werden über eine sequentielle zweistufige Hydroborierung an Bis(triethoxysilyl)ethene und ein Alken oder ein ungesättigtes Polymer erhalten. Über den zweiten Schritt wird hierbei die so genannte strukturgebende Gruppe eingeführt und damit das Template kovalent gebunden. Dadurch entfällt im Vergleich zum bekannten Nanocasting-Mechanismus zum einen die Verwendung des herkömmlichen Templates für die Bildung der Porenstruktur und zusätzlich führt die Mikrophasenseparation während der Kondensation zu einer Anordnung der strukturgebenden Gruppen des Precursors an der Silikatphasengrenze. Nach der chemischen Abspaltung dieser Gruppen, die gleichzeitig zur Einführung funktioneller Gruppen führt, werden somit hochporöse Organosilikate erhalten, in denen sich die funktionellen Gruppen ausschließlich an der Porenoberfläche befinden. Ein Vorteil der Verwendung der Hydroborieung wird in der Vielfalt der funktionellen Gruppen deutlich, die eingeführt werden können. Die Zugänglichkeit der funktionellen Gruppen ist entscheidend für potentielle Anwendungen und bei herkömmlichen Organosilikaten nicht zwangsläufig gegeben. Ein herausragender Aspekt dieses Konzepts besteht in der Möglichkeit, sehr einfach chirale Precursoren und damit Organosilikate mit hoch funktionalisierten, chiralen Oberflächen herzustellen. Es konnte gezeigt werden, dass sich diese Materialien sowohl für die chromatographische Trennung von Racematen mittels HPLC als auch für die asymmetrische Katalyse eignen. Durch die in dieser Arbeit erhaltenen Ergebnisse konnten wertvolle Erkenntnisse zur Ober-flächenfunktionalisierung und Strukturierung von mesoporösen Silikaten gewonnen werden. Die Möglichkeit, das vorgestellte Konzept auf andere strukturgebende Gruppen wie zum Beispiel Mesogene zu übertragen und damit die Porenmorphologie gezielt zu steuern, eröffnet viele weitere interessante Materialeigenschaften.

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Parameswaran, Priya. "Photoresponsive glasses: Control of physical and chemical effects in hybrid organosilica sol-gels with light /". Available to subscribers only, 2006. http://proquest.umi.com/pqdweb?did=1136089781&sid=12&Fmt=2&clientId=1509&RQT=309&VName=PQD.

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Libros sobre el tema "Organosilica"

McInall, Mark David. Non-ionic surfactant assembly of nanoporous organosilica frameworks. Sudbury, Ont: Laurentian University, School of Graduate Studies, 2006.

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Ha, Chang-Sik y Sung Soo Park. Periodic Mesoporous Organosilicas. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-2959-3.

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Chandra, Grish, ed. Organosilicon Materials. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-540-68331-5.

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I͡A, Lukevit͡s Ė. Nucleoside synthesis: Organosilicon methods. New York: Ellis Horwood, 1991.

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Alan, Bassindale y Gaspar P. P, eds. Frontiers of organosilicon chemistry. Cambridge: Royal Society of Chemistry, 1991.

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I͡A, Lukevit͡s Ė. Molecular structure of organosilicon compounds. Chichester: E. Horwood, 1989.

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Alekseev, P. G. Thermophysical properties of organosilicon compounds: A handbook. New York: Begell House, 1996.

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Johann, Weis y Auner Norbert, eds. Organosilicon chemistry V: From molecules to materials. Weinheim: Wiley-VCH, 2003.

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Weis, Johann y Norbert Auner. Organosilicon chemistry III: From molecules to materials. Weinheim: Wiley-VCH, 1998.

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Whittaker, Stephen Mark. Some chemistry of sterically hindered organosilicon compounds. Salford: University of Salford, 1993.

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Capítulos de libros sobre el tema "Organosilica"

Qiao, Shiz Zhang, Lian Zhou Wang, Qiu Hong Hu, Zhong Hua Zhu y Gao Qing Max Lu. "Synthesis of Highly Ordered Large-Pore Periodic Mesoporous Organosilica Rods". En Solid State Phenomena, 381–84. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-30-2.381.

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Florek, Justyna, Dominic Larivière y Freddy Kleitz. "Nanostructured Organosilica Hybrids as Highly Efficient and Regenerable Sorbents for Rare Earth Extraction". En ACS Symposium Series, 107–17. Washington, DC: American Chemical Society, 2016. http://dx.doi.org/10.1021/bk-2016-1224.ch006.

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Willai, Stéphanie, Maryse Bacquet y Michel Morcellet. "Organosilica Mesoporous Materials with Double Functionality: Amino Groups and β-Cyclodextrin Synthesis and Properties". En Silicon Based Polymers, 213–21. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-8528-4_15.

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Lockwood, Sarah B. y Bakul C. Dave. "A Closer Look at “Green” Glass: Remediation with Organosilica Sol-Gels Through the Application of Green Chemistry". En Green Chemistry for Environmental Remediation, 699–727. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118287705.ch22.

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Barton, Thomas J. y Philip Boudjouk. "Organosilicon Chemistry". En Advances in Chemistry, 3–46. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/ba-1990-0224.ch001.

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Rochow, Eugene G. "Organosilicon Compounds". En Inorganic Syntheses, 50–56. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132340.ch13.

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Hiyama, Tamejiro y Eiji Shirakawa. "Organosilicon Compounds". En Topics in Current Chemistry, 61–85. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45313-x_3.

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Krska, Shane W., David Y. Son y Dietmar Seyferth. "Organosilicon Dendrimers". En Silicon-Containing Polymers, 615–41. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-3939-7_23.

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Borst, Christopher L., William N. Gill y Ronald J. Gutmann. "CMP of Organosilicate Glasses". En Chemical-Mechanical Polishing of Low Dielectric Constant Polymers and Organosilicate Glasses, 97–118. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-1165-6_5.

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Moberg, William K., Gregory S. Basarab, John Cuomo y Paul H. Liang. "Biologically Active Organosilicon Compounds". En ACS Symposium Series, 288–301. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0355.ch026.

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Actas de conferencias sobre el tema "Organosilica"

Corrie, Simon, Gwen Lawrie, Bronwyn Battersby y Matt Trau. "Organosilica Particles for DNA Screening Applications". En 2006 International Conference on Nanoscience and Nanotechnology. IEEE, 2006. http://dx.doi.org/10.1109/iconn.2006.340599.

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Edmiston, Paul L., Justin Keener, Scott Buckwald, Bob Sloan y John Terneus. "Flow Back Water Treatment Using Swellable Organosilica Media". En SPE Eastern Regional Meeting. Society of Petroleum Engineers, 2011. http://dx.doi.org/10.2118/148973-ms.

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Fu, Shuang, Ke-Jia Qian, Shi-Jin Ding, Wei Zhang y Zhong-yong Fan. "Characterization of ultra-low k porous organosilica thin films". En 2010 10th IEEE International Conference on Solid-State and Integrated Circuit Technology (ICSICT). IEEE, 2010. http://dx.doi.org/10.1109/icsict.2010.5667532.

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Cui, Yan, Bin Ren, Rui Wang, Jun Zhang, Ning-Shao Xia, Zhong-Qun Tian, P. M. Champion y L. D. Ziegler. "Metal Core Organosilica Shell Multifunctional Nanoparticles for Multimodal Cell Imaging". En XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482267.

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CZECHURA, KRYSTYNA y ABDELHAMID SAYARI. "PHOTORESPONSIVE MESOPOROUS ORGANOSILICA WITH MOLECULAR ORDER IN THE PORE WALLS". En Proceedings of the 5th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812779168_0013.

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Reisr, Glaydson Simões dos, Carlos Hoffmann Sampaior, Eder Claudio Lima, Amilton Feliciano Castro y Irineu Antônio Schadach de Brum. "HYDROPHOBIC ORGANOSILICA ADSORBENTS FOR REMOVAL OF SODIUM DICLOFENAC FROM AQUEOUS SOLUTIONS". En 71º Congresso Anual da ABM. São Paulo: Editora Blucher, 2017. http://dx.doi.org/10.5151/1516-392x-27786.

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Abdullah, P. Pertiwi, I., D. U. C. Rahayu y Y. K. Krisnandi. "Synthesis and characterization of nickel immobilized on aminated Periodic Mesoporous Organosilica". En 3RD INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0062169.

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Zhang, Jiawei, Guoping Zhang, Rong Sun, S. W. Ricky Lee y C. P. Wong. "Low-dielectric-constant novel periodic mesoporous organosilica thin film for interlayer dielectric". En 2016 17th International Conference on Electronic Packaging Technology (ICEPT). IEEE, 2016. http://dx.doi.org/10.1109/icept.2016.7583109.

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Henning, Torsten, Juergen J. Brandner, Lutz Eichhorn, Klaus Schubert, Martin Schreiber, Martin Gu¨ngerich, Hermann Gu¨nther, Peter J. Klar, Vivian Rebbin y Michael Fro¨ba. "Selective Adsorption of Solvents in a Multiscale Device". En ASME 4th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2006. http://dx.doi.org/10.1115/icnmm2006-96190.

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Resumen

We have incorporated microspheres, 50 μm to 80 μm in diameter, of periodic mesoporous organosilica (inner surfaces up to 1000 m2/g and pore sizes in the nanometre range) with two types of organic functionalities (benzene and ethane bridges, respectively) inside microstructured channels (each 200 μm wide and 100 μm deep) and, exemplarily, monitored by Raman microscopy that the temperature characteristics of the adsorption-desorption equilibria of benzene and ethanol vary significantly with the type of organic functionality of the microspheres and the pore morphology. The integration of this class of nanostructured material into devices by means of microchannels is a promising novel approach to, among others, substance separation in analytics, micro process engineering, and micro chemistry.

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Yang, Shu, Yun Liu, Huamin Yi, Liquan Sun y Aiqin Luo. "Preparation and characterization of molecularly imprinted mesoporous organosilica for biphenol Z recognition and separation". En 2015 IEEE International Conference on Mechatronics and Automation (ICMA). IEEE, 2015. http://dx.doi.org/10.1109/icma.2015.7237617.

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Informes sobre el tema "Organosilica"

Zhao, G. Synthesis of organosilicon compounds. Office of Scientific and Technical Information (OSTI), enero de 1996. http://dx.doi.org/10.2172/453770.

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Xie, Ren. Syntheses and studies of organosilicon compounds. Office of Scientific and Technical Information (OSTI), febrero de 1999. http://dx.doi.org/10.2172/348883.

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Seyferth, Dietmar. Organosilicon Compounds and Polymers and Silicon Ceramics. Fort Belvoir, VA: Defense Technical Information Center, marzo de 1989. http://dx.doi.org/10.21236/ada206589.

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Fenton, Kyle R., Ganesan Nagasubramanian, Chad L. Staiger, Harry D. Pratt, III, Susan B. Rempe, Kevin Leung, Mangesh I. Chaudhari y Travis Mark Anderson. Organosilicon-Based Electrolytes for Long-Life Lithium Primary Batteries. Office of Scientific and Technical Information (OSTI), septiembre de 2015. http://dx.doi.org/10.2172/1222982.

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Parikh, Bosky. Synthesis, characterization and catalytic studies of N-doped ordered mesoporous carbons and functionalized periodic mesoporous organosilicas. Office of Scientific and Technical Information (OSTI), diciembre de 2017. http://dx.doi.org/10.2172/1505185.

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Kim, H. C. Templating Organosilicate Vitrification Using Unimolecular Self Organizing Polymers: Evolution of Morphology and Nanoporosity Development with Network Formation. Office of Scientific and Technical Information (OSTI), diciembre de 2004. http://dx.doi.org/10.2172/839714.

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