Bibliografías temáticas / Oxide

Literatura académica sobre el tema "Oxide"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 8 de junio de 2024

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Artículos de revistas sobre el tema "Oxide"

1

She, Weiqing, Zhenzhen Xu, Lianjie Zhai, Junlin Zhang, Jie Huang, Weiqiang Pang y Bozhou Wang. "Synthetic Methods Towards Energetic Heterocyclic N-Oxides via Several Cyclization Reactions". Crystals 12, n.º 10 (25 de septiembre de 2022): 1354. http://dx.doi.org/10.3390/cryst12101354.

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Due to the introduction of oxygen atoms, N-oxide energetic compounds have a unique oxygen balance, excellent detonation properties, and a high energy density, attracting the extensive attention of researchers all over the world. N-oxides are classified into two categories based on the structural characteristics of their skeletons: azine N-oxides and azole N-oxides, whose N→O coordination bonds are formed during cyclization. There are six kinds of azine N-oxides, namely 1,2,3,4-tetrazine-1,3-dioxide, 1,2,3,5-tetrazine-2-oxide, 1,2,3-triazine-3-oxide, 1,2,3-triazine-2-oxide, pyridazine-1,2-dioxide, and pyrazine-1-oxide. Azole N-oxides include 1,2,5-oxadiazole-2-oxide, pyrazole-1-oxide, and triazole-1-oxide. Synthetic strategies towards these two categories of N-oxides are fully reviewed. Corresponding reaction mechanisms towards the aromatic N-oxide frameworks and examples that use the frameworks to create high-energy substances are discussed. Moreover, the energetic properties of N-oxide energetic compounds are compared and summarized.
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2

Möhrle, H. y R. Nießen. "Reaktionen von Isochinolinium-Salzen mit Hydroxylamin-Derivaten, 2. Mitteilung N-(Alkyl)- und N-(Aryl)-substituierte Verbindungen / Reactions of Isoquinolinium Salts with Hydroxylamine Derivatives, 2nd Communication N-(Alkyl) and N-(Aryl) Substituted Compounds". Zeitschrift für Naturforschung B 54, n.º 4 (1 de abril de 1999): 532–40. http://dx.doi.org/10.1515/znb-1999-0417.

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The N -alkyl- and N -aryl-isoquinolinium salts 7, 15-17 reacted with free hydroxylamine in pyridine to give the isoquinoline-2-oxide (9) as final product. The intermediate dioximes 8 were isolated and characterized by derivatisation with acetic anhydride to the oxime ester nitrile 10. From the reaction o f 8 with trifluoroacetic anhydride/triethylam ine 3-amino-isoquinoline- 2-oxide (12) resulted after hydrolysis. Due to the electronic influence the 5-nitroisoquinolinium salts 1 -3 react faster than the 5-hydroxy derivative 20. but with the same course of conversion via dioximes to amine oxides. An optimized method for preparation of the amine oxides was developed .
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3

Kim, Youngsun, Donghee Choi, Hosun Jang, Changsu Na, Moonhyeon Hwang, Joohyun Cho, Kyoungin Lee, Sunmin Kim, Byoungsik Pyo y Daehwan Youn. "Effects of Acupuncture at ST41, BL60, GB38 on Changes of Nitric Oxide and Nitric Oxide Synthase in Rats". Korean Journal of Acupuncture 30, n.º 2 (27 de junio de 2013): 97–103. http://dx.doi.org/10.14406/acu.2013.30.2.097.

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Cha, Wu-Shin, Junsik Lee, Malkeshkumar Patel, Kibum Lee y Joondong Kim. "Flexible and Transparent Heater with Oxide/Metal/Oxide Structure". Transactions of The Korean Institute of Electrical Engineers 72, n.º 1 (31 de enero de 2023): 87–92. http://dx.doi.org/10.5370/kiee.2023.72.1.87.

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Majhi, Sanjit Manohar, Ali Mirzaei, Hyoun Woo Kim y Sang Sub Kim. "Reduced Graphene Oxide (rGO)-Loaded Metal-Oxide Nanofiber Gas Sensors: An Overview". Sensors 21, n.º 4 (14 de febrero de 2021): 1352. http://dx.doi.org/10.3390/s21041352.

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Reduced graphene oxide (rGO) is a reduced form of graphene oxide used extensively in gas sensing applications. On the other hand, in its pristine form, graphene has shortages and is generally utilized in combination with other metal oxides to improve gas sensing capabilities. There are different ways of adding rGO to different metal oxides with various morphologies. This study focuses on rGO-loaded metal oxide nanofiber (NF) synthesized using an electrospinning method. Different amounts of rGO were added to the metal oxide precursors, and after electrospinning, the gas response is enhanced through different sensing mechanisms. This review paper discusses rGO-loaded metal oxide NFs gas sensors.
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6

Novosyolov, A., I. Olianina, I. Novoselova, Y. Vasina, Y. Ershova, T. Loik y Yu Kudelina. "RESEARCH OF THE POSSIBILITY OF REDUCING THE CIRCULATION OF SULFUR OXIDE IN THE PRODUCTION OF WHITE CEMENT". Bulletin of Belgorod State Technological University named after. V. G. Shukhov 6, n.º 7 (10 de julio de 2021): 89–98. http://dx.doi.org/10.34031/2071-7318-2021-6-7-89-98.

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The article discusses the possibility of reducing the circulation of sulfur oxide in the production of white cement by introducing alkaline potassium oxides K2O and sodium Na2O. A decrease in the circulation of sulfur oxide SO3 is achieved by increasing its yield in the clinker by transferring SO3 from a more sublimated compound of calcium sulfate CaSO4 to less sublimated potassium sulfates K2SO4 and sodium Na2SO4. Potassium and sodium oxides are introduced in the composition of carbonates and feldspar. The amount of introduced alkali oxides is controlled by the molar ratio A/S between sulfur oxide SO3 and alkaline oxides K2O and Na2O. It is shown that with the same molar ratio between sulfur oxide and alkaline oxides, the amount of SO3 removed with clinker depends on the ratio between potassium and sodium oxides. The higher the sodium oxide content, the more sulfur oxide comes out with the clinker and less remains to circulate in the kiln. The sublimation of sulfur oxide decreases from 70.5% - without the introduction of alkaline oxides, to 38,5 % at the maximum A/S ratio with the addition of potassium and sodium oxides in a ratio of 80:20 %. When potassium and sodium oxides are added in a ratio of 20:80%, the sublimation of sulfur oxide is reduced to 7,7 % at the same A/S ratio.
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7

Pourroy, G., J. L. Guille y P. Poix. "Reactivity of metal oxides copper(I) oxide, manganese(II) oxide, cobalt(II) oxide, nickel(II) oxide, copper(II) oxide and zinc oxide with indialite". Chemistry of Materials 2, n.º 2 (marzo de 1990): 101–5. http://dx.doi.org/10.1021/cm00008a007.

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Li, Huaying y Aichun Zhao. "Pickling Behavior of Duplex Stainless Steel 2205 in Hydrochloric Acid Solution". Advances in Materials Science and Engineering 2019 (25 de febrero de 2019): 1–6. http://dx.doi.org/10.1155/2019/9754528.

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The oxide-scale structure and pickling behavior of oxided 2205 duplex stainless steel in the electrolytes containing hydrochloric acid were investigated. The oxide scales mainly consist of two layers: the outer layer is dense Fe2O3, and the inner granular is FeCr2O4 spinel. During the pickling process, pittings form around the boundaries of FeCr2O4 particles or interfaces of two kinds of oxides, which results in that the electrolyte can directly react with the chromium-depleted layer along the pittings to produce an “undercut” effect so that the pickling efficiency is improved markedly. The pickling mechanism was discussed, and the model was established.
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9

Read, RW y WP Norris. "The Nucleophilic Substitution Reactions of 5- and 7-Chloro-4,6-dinitrobenzofurazan 1-Oxide by Aromatic Amines." Australian Journal of Chemistry 38, n.º 3 (1985): 435. http://dx.doi.org/10.1071/ch9850435.

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7-Chloro-4,6-dinitrobenzofurazan 1-oxide is a powerful electrophile which reacts with a variety of primary and secondary aromatic amines, even those with deactivating substituents , to give arylamino - benzofurazan oxides under mild conditions. Tertiary aromatic amines react through carbon to give aminoarylbenzofurazan oxides. During, or as a consequence of, the substitution reactions, tautomerism occurs to give in all but one example an equilibrium mixture of 5- and 7-substituted 4,6-dinitrobenzofurazan oxides in which the latter predominates. Thus 5-chloro-4,6-dinitrobenzofurazan 1-oxide and 7- chloro-4,6-dinitrobenzofurazan 1-oxide both react with aniline to yield the same isomeric mixture of products: 4,6-dinitro-7- phenylaminobenzofurazan oxide (predominantly 1-oxide) (major) and 4,6- dinitro-5-phenylaminobenzofurazan 1-oxide (minor). The 5- and 7- phenylamino 4,6-dinitrobenzofurazans were prepared to assist in structural assignment of the N-oxides.
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10

Navrotsky, Alexandra y Anastasia Koryttseva. "Acid–Base Properties of Oxides Derived from Oxide Melt Solution Calorimetry". Molecules 28, n.º 12 (7 de junio de 2023): 4623. http://dx.doi.org/10.3390/molecules28124623.

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The paper analyzes the relationships among acid–base interactions in various oxide systems and their thermodynamics. Extensive data on enthalpies of solution of binary oxides in oxide melts of several compositions, obtained by high-temperature oxide melt solution calorimetry at 700 and 800 °C, are systematized and analyzed. Oxides with low electronegativity, namely the alkali and alkaline earth oxides, which are strong oxide ion donors, show enthalpies of solution that have negative values greater than −100 kJ per mole of oxide ion. Their enthalpies of solution become more negative with decreasing electronegativity in the order Li, Na, K and Mg, Ca, Sr, Ba in both of the commonly used molten oxide calorimetric solvents: sodium molybdate and lead borate. Oxides with high electronegativity, including P2O5, SiO2, GeO2, and other acidic oxides, dissolve more exothermically in the less acidic solvent (lead borate). The remaining oxides, with intermediate electronegativity (amphoteric oxides) have enthalpies of solution of between +50 and −100 kJ/mol, with many close to zero. More limited data for the enthalpies of solution of oxides in multicomponent aluminosilicate melts at higher temperature are also discussed. Overall, the ionic model combined with the Lux–Flood description of acid–base reactions provide a consistent and useful interpretation of the data and their application for understanding the thermodynamic stability of ternary oxide systems in solid and liquid states.
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Tesis sobre el tema "Oxide"

1

Gillispie, Meagen Anne. "Metal oxide-based transparent conducting oxides". [Ames, Iowa : Iowa State University], 2006.

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2

Field, Marianne Alice Louise. "Transition metal oxides and oxide-halides". Thesis, University of Southampton, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.401833.

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Boltz, Janika [Verfasser]. "Sputtered tin oxide and titanium oxide thin films as alternative transparent conductive oxides / Janika Boltz". Aachen : Hochschulbibliothek der Rheinisch-Westfälischen Technischen Hochschule Aachen, 2012. http://d-nb.info/1019850485/34.

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Messi, C. "Nanostructured catalytic metal oxides supported over oxide supports of various nature : the iron oxide system". Doctoral thesis, Università degli Studi di Milano, 2008. http://hdl.handle.net/2434/57081.

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Sayle, D. C. "Computer simulation of heteroepitaxial oxide/oxide and metal/oxide interfaces". Thesis, University of Bath, 1992. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317429.

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Lockyer, D. M. "Adsorption and reaction of cyanogen with copper oxide, chromium oxide and copper oxide-chromium oxide surfaces". Thesis, University of Bath, 1988. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383244.

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7

Reeder, Askia Enrico. "STUDY OF THE STRUCTURE AND THE ELECTRONIC PROPERTIES OF THE OXIDE/OXIDE INTERFACES IN MIXED METAL OXIDES". Doctoral thesis, Università degli studi di Padova, 2014. http://hdl.handle.net/11577/3423844.

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A very important role is played by metal oxides in many areas of chemistry, physics, and materials science. Transition metal and rare-earth metal elements are able to form a large diversity of oxide compounds which can adopt an ample array of atomic structures and electronic properties that can exhibit metallic, semiconductor, or insulator characteristics. In technological applications, metal oxides are used in the fabrication of microelectronic components, sensors, fuel cells, coatings to protect surfaces against corrosion, and as catalysts. In this thesis we have decided to study two known catalytic materials Zirconia-Titania and Ceria-Titania mixed oxides. For both materials bibliography principally concerns powders thus in order to better study their interfaces, of which a deeper study is still lacking, we decided to deposit zirconia and ceria as thin films onto rutile TiO2(110). We first studied the zirconia-titania system by depositing an ultra-thin film of zirconium oxide via a metal-organic precursor: Zirconium Tetra tert-Butoxide. The deposition was carried at three different substrate temperatures 677 K, 738 K, 773 K in five stages of a minute each and the results were traced by using XPS. The chemical characterization via XPS showed an interesting chemistry undergoing on the substrate’s surface and we have observed the formation of carbonaceous species at the interface. Zirconium appeared to be at its highest oxidation state while titanium was seen to undergo reduction with each successive deposited layer. The ratio of the Zr/Ti signals showed that zirconia didn’t completely wet the surface. Furthermore, no long range order was observed via LEED. XPD measurements showed that zirconia does not form a substitutional oxide with titania. However with the aid of computer simulation we deduced that very likely zirconia forms nanochains on the surface of TiO2(110). This surface was exposed to 100 L of pyridine to test its acidity. In the case of ceria, we have deposited the oxide on a heated TiO2(110) substrate via metal evaporation from a Mo crucible since the process is rather easy and garners clean deposits. During deposition the substrate was kept at 677 K and in an O2 environment of 5.2•10-6mbar, and, in order to obtain an ordered homogeneous surface the sample was further annealed in the same environment at 900 K. Through LEED imaging different phases were observed and were dependent on sample history and film thickness. Via computer simulation these phases were then referred to the parent oxide in order to better comprehend the difference in respect to the bulk phase. All films showed cerium present at Ce(III). Ultra-violet Photoelectron Spectroscopy showed the electronic properties of the film showing a binding energy shift and the population of Ce4f states due to stabilization of Ce(III) by TiO2(110). The reactivity of the ceria-titania system was the probed by using methanol and ethanol. Results showed that the addition of ceria opened the dehydrogenation path from alcohol to aldehyde. We have observed that oxygen pre-oxidation of the CeOx-TiO2(110) system had an impact on its selectivity by opening also a dehydration path from methanol and ethanol to respectively, methane and ethylene. This alternative path was viable only for low cerium oxide coverages as interaction with the substrate was needed for dehydration to occur. Aldehyde formation was seen to occur at mild temperatures (330 K) and was independent of film thickness. Subsequently, ceria-titania mixed oxide powders were characterized via XPS and we have observed that for increasing amount of cerium the element gradually became present at its highest oxidation state Ce(IV). By XPS we have also determined the formation of a very intimate composite between the two oxides by observing the increasing the full width at half maximum of the Ti2p peak for increasing amounts of cerium. Furthermore, compositional calculation showed that cerium had the tendency to disperse within the titania particles. These data helped to uncover a possibly good recipe for the formation of cerium titanate a composite with good oxygen storage capacity.
Un ruolo molto importante è svolto dagli ossidi metallici in molti settori della chimica, fisica e scienza dei materiali. I metalli di transizione e le terre rare sono in grado di formare una grande diversità di composti ossidici che possono adottare un'ampia gamma di strutture atomiche ed proprieta’ elettroniche che possono esibire caratteristiche metalliche, semiconduttrici o isolanti. In applicazioni tecnologiche, gli ossidi metallici sono impiegati nella fabbricazione di componenti microelettronici, sensori, celle a combustibile, rivestimenti per proteggere le superfici dalla corrosione, e come catalizzatori. In questa tesi abbiamo deciso di studiare due noti materiali catalitici: gli ossidi misti di Zirconia-Titania Ceria-Titania. Per entrambi i materiali la bibliografia riguarda principalmente le polveri quindi, al fine di studiare meglio le loro interfacce, di cui uno studio più approfondito e’ tuttora neccessario, abbiamo deciso di depositare film sottili di ossido di zirconio e ossido di cerio su rutilo TiO2(110). Abbiamo prima studiato il sistema zirconia-titania depositando un film ultra-sottile di ossido di zirconio mediante un precursore metallo-organico: Zirconio Tetra tert-butossido. La deposizione è stata effettuata a tre diverse temperature del substrato 677. K, 738 K, 773 K in cinque fasi di un minuto ciascuno. La caratterizzazione mediante XPS ha mostrato una chimica interessante sulla superficie del substrato e abbiamo osservato la formazione di specie carboniose all'interfaccia. Lo zirconio sembrava essere nel suo piu’ alto stato di ossidazione mentre il titanio è stato visto gradualmente ridursi con ogni successive strato di deposito. Il rapporto dei segnali Zr/Ti ha mostrato che la zirconia non ha completamente coperto la superficie. Inoltre,tramite LEED non si e’ osservato nessun ordine a lungo raggio. Misure XPD ha mostrato che la zirconia non forma un ossido di sostituzione con la titania. Tuttavia, con l'ausilio di simulazione al computer abbiamo dedotto che la zirconia forma, molto probabilmente nanocatene sulla superficie di TiO2(110). Questa superficie è stato esposta a 100 L di pyridinina per testarne la acidita’. Nel caso di ceria, abbiamo depositato l'ossido su un substrato riscaldato di TiO2 (110) tramite evaporazione del metallo da un crogiolo Mo poiché il processo è piuttosto facile e fornisce depositi puliti. Durante la deposizione il substrato è stata mantenuto a 677 K in un ambiente di 5,2 • 10 -6 mbar di O2, e, al fine di ottenere una superficie omogenea e ordinata il campione è stato ulteriormente sottoposto a trattamento termico nello stesso ambiente a 900 K. Tramite la tecnica LEED sono state osservate differenti fasi dipendenti dalla storia del campione e dallo spessore del film. Tramite simulazione al computer queste fasi sono stati poi riferite rispetto al biossido di cerio per meglio comprendere le differenze rispetto alla fase massiva. Tutti i film hanno mostrato cerio presenti come Ce(III). La Spettroscopia Fotoelettronica a Ultravioletti ha mostrato le proprietà elettroniche del film che mostra uno spostamento in energia di legame e un popolamento degli stati Ce4f. Questo e’ dovuto alla stabilizzazione di Ce (III) da parte di TiO2 (110). Si e’ volute osservare la reattività del sistema ceria-titania nei confronti di metanolo ed etanolo. I risultati hanno mostrato che l'aggiunta di ceria ha aperto il percorso della deidrogenazione degli alcoli ad aldeidi. Abbiamo osservato che la pre-ossidazione con ossigeno del sistema CeOx-TiO2(110) ha avuto un impatto sulla sua selettività aprendo anche un percorso di disidratazione di metanolo ed etanolo rispettivamente a metano ed etilene. Questa via alternativa era valida solo per basse coperture di ossido di cerio avendo osservato che l’interazione con il substrato è stato necessario perche’ avvenga la disidratazione. La formazione di aldeidi fu osservata avvenire a temperature piuttosto (330 K) ed essere indipendente dallo spessore del film. Successivamente sono state caratterizzate tramite XPS delle polveri di ossidi misti di ceria e titania. Abbiamo osservato che per quantità crescenti di cerio l'elemento diventa gradualmente sempre piu’ presente al suo stato di ossidazione più alto Ce (IV). Con XPS abbiamo anche determinato la formazione di un composito molto intimo tra i due ossidi osservando l'aumento della larghezza a metà altezza del picco Ti2p per quantità crescenti di cerio. Inoltre, la determinazione della composizione ha mostrato che il cerio ha la tendenza di disperdersi all'interno delle particelle di titania. Questi dati hanno contribuito a scoprire una possibile buona ricetta per la formazione di cerio titanato; un composito con buona capacità di stoccaggio di ossigeno.
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Burkardt, Sven. "Oxide and oxide supported nanoclusters on quasicrystals". Berlin Logos-Verl, 2009. http://d-nb.info/999419471/04.

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Zhang, Huichun. "Metal oxide-facilitated oxidation of antibacterial agents". Diss., Available online, Georgia Institute of Technology, 2004:, 2004. http://etd.gatech.edu/theses/available/etd-07072004-152317/unrestricted/zhang%5Fhuichun%5F200407%5Fphd.pdf.

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Thesis (Ph. D.)--School of Civil and Environmental Engineering, Georgia Institute of Technology, 2005. Directed by Ching-Hua Huang.
Wine, Paul, Committee Member ; Pavlostathis, Spyros, Committee Member ; Mulholland, James, Committee Member ; Yiacoumi, Sotira, Committee Member ; Huang, Ching-Hua, Committee Chair. Includes bibliographical references.
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Taujale, Saru. "INTERACTIONS BETWEEN METAL OXIDES AND/OR NATURAL ORGANIC MATTER AND THEIR INFLUENCE ON THE OXIDATIVE REACTIVITY OF MANGANESE DIOXIDE". Diss., Temple University Libraries, 2015. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/347169.

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Civil Engineering
Ph.D.
Mn oxides have high redox potentials and are known to be very reactive, rendering many contaminants susceptible to degradation via oxidation. Although Mn oxides typically occur as mixtures with other metal oxides (e.g., Fe, Al, and Si oxides) and natural organic matter (NOM) in soils and aquatic environments, most studies to date have studied the reactivity of Mn oxides as a single oxide system. This study, for the first time, examined the effect of representative metal oxides (Al2O3, SiO2, TiO2, and Fe oxides) and NOM or NOM-model compounds (Aldrich humic acid (AHA), Leonardite humic acid (LHA), pyromellitic acid (PA) and alginate) on the oxidative reactivity of MnO2, as quantified by the oxidation kinetics of triclosan (a widely used phenolic antibacterial agent) as a probe compound. The study also examined the effect of soluble metal ions released from the oxide surfaces on MnO2 reactivity. In binary oxide mixtures, Al2O3 decreased the reactivity of MnO2 as a result of both heteroaggregation and complexation of soluble Al ions with MnO2. At pH 5, the surface charge of MnO2 is negative while that of Al2O3 is positive resulting in intensive heteroaggregation between the two oxides. Up to 3.15 mM of soluble Al ions were detected in the supernatant of 10 g/L of Al2O3 at pH 5.0 whereas the soluble Al concentration was 0.76 mM in the mixed Al2O3 + MnO2 system at the same pH. The lower amount of soluble Al in the latter system is the result of Al ion adsorption by MnO2. The experiments with the addition of 0.001 to 0.1 mM Al3+ to MnO2 suspension indicated the triclosan oxidation rate constant decreased from 0.24 to 0.03 h-1 due to surface complexation. Fe oxides which are also negatively charged at pH 5 inhibited the reactivity of MnO2 through heteroaggregation. The concentration of soluble Fe(III) ions ( 4 mg-TOC/L or [alginate/PA] > 10 mg/L, a lower extent of heteroaggregation was also observed due to the negatively charged surfaces for all oxides. Similar effects on aggregation and MnO2 reactivity as discussed above were observed for ternary MnO2‒Al2O3‒NOM systems. HAs, particularly at high concentrations (2.0 to 12.5 mg-C/L), alleviated the effect of soluble Al ions on MnO2 reactivity as a result of the formation of soluble Al-HA complexes. Alginate and PA, however, did not form soluble complexes with Al ions so they did not affect the effect of Al ions on MnO2 reactivity. Despite the above observations, the amount of Al ions dissolved in MnO2+Al2O3+NOM mixtures was too low, as a result of NOMs adsorption on the surface to passivate oxide dissolution, to have a major impact on MnO2 reactivity. In conclusion, this study provided, for the first time, a systematical understanding of the redox activity of MnO2 in complex model systems. With this new knowledge, the gap between single oxide systems and complex environmental systems is much narrower so that it is possible to have a more accurate prediction of the fate of contaminants in the environment.
Temple University--Theses
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Libros sobre el tema "Oxide"

1

Surface Chemistry Studies of Transition Metal Oxides: Titanium Oxide and Iron Oxide. [New York, N.Y.?]: [publisher not identified], 2015.

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Ishihara, Tatsumi, ed. Perovskite Oxide for Solid Oxide Fuel Cells. Boston, MA: Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-77708-5.

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Chowdhury, Geeta, Boguslaw Kruczek y Takeshi Matsuura, eds. Polyphenylene Oxide and Modified Polyphenylene Oxide Membranes. Boston, MA: Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1483-1.

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Perovskite oxide for solid oxide fuel cells. Dordrecht: Springer, 2009.

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Mayer, Bernd, ed. Nitric Oxide. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3.

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Higashiwaki, Masataka y Shizuo Fujita, eds. Gallium Oxide. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-37153-1.

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Dimiev, Ayrat M. y Siegfried Eigler, eds. Graphene Oxide. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119069447.

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Klingshirn, Claus F., Bruno K. Meyer, Andreas Waag, Axel Hoffmann y Jean Geurts. Zinc Oxide. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10577-7.

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McCarthy, Helen O. y Jonathan A. Coulter, eds. Nitric Oxide. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61737-964-2.

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Gao, Wei, ed. Graphene Oxide. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15500-5.

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Capítulos de libros sobre el tema "Oxide"

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Keller, Kristin A., George Jefferson y Ronald J. Kerans. "Oxide-Oxide Composites". En Ceramic Matrix Composites, 236–72. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118832998.ch8.

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Stoneham, A. M. y P. W. Tasker. "Oxide Interfaces: Theory of Oxide-Oxide and Oxide-Metal Interfaces". En Ceramic Microstructures ’86, 155–65. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1933-7_16.

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Moncada, S. "Introduction". En Nitric Oxide, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_1.

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Balligand, J. L. "Regulation of Cardiac Function by Nitric Oxide". En Nitric Oxide, 207–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_10.

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McNaughton, L., A. Radomski, G. Sawicki y Marek W. Radomski. "Regulation of Platelet Function". En Nitric Oxide, 235–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_11.

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Garthwaite, J. "The Physiological Roles of Nitric Oxide in the Central Nervous System". En Nitric Oxide, 259–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_12.

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Martin, W. "The Role of Nitric Oxide in the Peripheral Nervous System". En Nitric Oxide, 277–313. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_13.

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Navarra, P., A. Costa y A. Grossman. "Nitric Oxide and Neuroendocrine Function". En Nitric Oxide, 315–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_14.

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Hackenthal, E. "The Role of Nitric Oxide in Kidney Function". En Nitric Oxide, 329–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_15.

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Kojda, G. "Therapeutic Importance of Nitrovasodilators". En Nitric Oxide, 365–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_16.

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Actas de conferencias sobre el tema "Oxide"

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Jurf, Robert A. y Steven C. Butner. "Advances in Oxide-Oxide CMC". En ASME 1999 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/99-gt-190.

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Recent advances in COI’s oxide-oxide CMC materials will be presented including basic processing steps, updated material properties, and fabrication techniques. Material properties of COI’s alumino-silicate system reinforced with various oxide fabrics will be compared, along with progress in developing a 1200°C oxide matrix system for future turbine system applications. Examples of fabricated hardware, including a subscale combustion liner, will be shown. Recent test and evaluation data will be provided.
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Chiang, Steve, Roger Wang, Jacob Chen, Ken Hayes, John McCollum, Esmat Hamdy y Chenming Hu. "oxide-Nitride-oxide Antifuse Reliability". En 28th International Reliability Physics Symposium. IEEE, 1990. http://dx.doi.org/10.1109/irps.1990.363520.

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Van de Walle, Chris G. "Doping of gallium oxide and aluminum gallium oxide alloys". En Oxide-based Materials and Devices XII, editado por Ferechteh H. Teherani, David C. Look y David J. Rogers. SPIE, 2021. http://dx.doi.org/10.1117/12.2588459.

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Rafitasari, Yeti, Haris Suhendar, Nurul Imani, Fitri Luciana, Hesti Radean y Iman Santoso. "SINTESIS GRAPHENE OXIDE DAN REDUCED GRAPHENE OXIDE". En SEMINAR NASIONAL FISIKA 2016 UNJ. Pendidikan Fisika dan Fisika FMIPA UNJ, 2016. http://dx.doi.org/10.21009/0305020218.

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Grundmann, Marius. "Trigonal oxide semiconductor heterostructures". En Oxide-based Materials and Devices XIII, editado por Ferechteh H. Teherani y David J. Rogers. SPIE, 2022. http://dx.doi.org/10.1117/12.2617537.

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Cao, Feng, Zhenyu Song, Yupeng An, Baojia Guo, Lei Li y Yiding Wang. "Highly transparent and conductive Tantalum-doped ZnO films prepared by radio frequency sputtering". En Oxide-based Materials and Devices. SPIE, 2010. http://dx.doi.org/10.1117/12.841286.

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Nagar, S. y S. Chakrabarti. "A detailed temperature dependent Hall study of As-doped ZnO thin films". En Oxide-based Materials and Devices. SPIE, 2010. http://dx.doi.org/10.1117/12.842013.

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Ohtani, N., T. Katayama, H. Yamamoto y H. Koyama. "Detection of Gate Oxide Defects Using Electrochemical Wet Etching in KOH:H2O Solution". En ISTFA 1997. ASM International, 1997. http://dx.doi.org/10.31399/asm.cp.istfa1997p0279.

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Abstract A new technique to detect gate oxide defects has been developed. This method is based on electrochemical wet (ECW) etching of Si in KOH:H 20 electrolyte. Using this method, only leaky poly-Si gates caused by gate oxide defects can be clearly observed. When applying a certain voltage to a Si substrate in KOH:H20 after exposing the polySi gates, normal poly-Si gates can be etched, but poly-Si gates shorted to the Si substrate through gate oxide defects remain unetched because of the anodic oxide which covers the leaky gate. This method has proved to be very effective in obtaining information concerning gate oxide integrity without direct observation of gate oxides, which requires complicated deprocessing and a lot of time. This technique also reveals electrical characteristics of gate oxides which may be difficult to identify by conventional physical analysis.
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Zhang, Dianyun, Pascal Meyer y Anthony M. Waas. "Tensile Response of Oxide/Oxide Woven Ceramic Composites". En 56th AIAA/ASCE/AHS/ASC Structures, Structural Dynamics, and Materials Conference. Reston, Virginia: American Institute of Aeronautics and Astronautics, 2015. http://dx.doi.org/10.2514/6.2015-0464.

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Felsch, C. y E. Rosenbaum. "The relation between oxide degradation and oxide breakdown". En Proceedings of 1995 IEEE International Reliability Physics Symposium. IEEE, 1995. http://dx.doi.org/10.1109/relphy.1995.513667.

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Informes sobre el tema "Oxide"

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Lei, Ming y Hassel Ledbetter. Oxides and oxide superconductors :. Gaithersburg, MD: National Institute of Standards and Technology, 1991. http://dx.doi.org/10.6028/nist.ir.3980.

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Lad, R. J. Structure, adhesion, and stability of metal/oxide and oxide/oxide interfaces. Office of Scientific and Technical Information (OSTI), enero de 1991. http://dx.doi.org/10.2172/6335383.

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Lad, R. J. Structure, adhesion, and stability of metal/oxide and oxide/oxide interfaces. Office of Scientific and Technical Information (OSTI), noviembre de 1992. http://dx.doi.org/10.2172/6895283.

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Lad, R. J. Structure, adhesion, and stability of metal/oxide and oxide/oxide interfaces. Office of Scientific and Technical Information (OSTI), enero de 1992. http://dx.doi.org/10.2172/5766870.

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Elliot R. Bernsteinq. Interactions of Neutral Vanadium Oxide & Titanium Oxide Clusters with Sufur Dioxides, Nitrogen Oxides and Water. Office of Scientific and Technical Information (OSTI), agosto de 2006. http://dx.doi.org/10.2172/890716.

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Jackson, Jay Matthew, Marisa Jennifer Monreal, Kirk Ryan Weisbrod, David Anthony Tyler Rodriguez y Michael F. Simpson. Electrolytic Oxide Reduction of Plutonium Oxide Surrogates. Office of Scientific and Technical Information (OSTI), octubre de 2018. http://dx.doi.org/10.2172/1475332.

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Egami, Takeshi y John M. Vohs. Utilizing metal-oxide and oxide-oxide interactions for improved automotive emissions control catalysts. Final report. Office of Scientific and Technical Information (OSTI), febrero de 2003. http://dx.doi.org/10.2172/810694.

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Wagner, R. A. Novel Oxide-Oxide Fiber Reinforced Hot Gas Filter Development. Office of Scientific and Technical Information (OSTI), diciembre de 1996. http://dx.doi.org/10.2172/419964.

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Metiu, Horia. Catalysis by Nanostructures: Methane, Ethylene Oxide, and Propylene Oxide. Fort Belvoir, VA: Defense Technical Information Center, diciembre de 2002. http://dx.doi.org/10.21236/ada409509.

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Lad, Robert J. Structural, electronic and chemical properties of metal/oxide and oxide/oxide interfaces and thin film structures. Office of Scientific and Technical Information (OSTI), diciembre de 1999. http://dx.doi.org/10.2172/758832.

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