Relevant bibliographies by topics / Surface structure, reactivity and catalysis

Contents

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

Academic literature on the topic 'Surface structure, reactivity and catalysis'

Author: Grafiati
Published: 17 September 2021
Last updated: 30 July 2025

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Journal articles on the topic "Surface structure, reactivity and catalysis"

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KIM, D. "Surface structure and reactivity of CrO3/SiO2 catalysts." Journal of Catalysis 136, no. 1 (1992): 209–21. http://dx.doi.org/10.1016/0021-9517(92)90120-7.

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Kim, Do Gun, Seong Won Im, Kyung Hwan Ryu, Seoung Ho Jo, Min Gyeong Choe, and Seok Oh Ko. "Dependency of Catalytic Reactivity on the Characteristics of Expanded Graphites as Representatives of Carbonaceous Materials." Molecules 30, no. 11 (2025): 2275. https://doi.org/10.3390/molecules30112275.

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Carbonaceous materials (CMs) have gained great attention as heterogeneous catalysts in water treatment because of their high efficiency and potential contribution to achieving carbon neutrality. Expanded graphite (EG) is ideal for studying CMs because the reactivity in CMs largely depends on graphitic structures, and most surface of EG is exposed, minimizing mass transfer resistance. However, EG is poor in adsorption and catalysis. In this study, EG was modified by simple thermal treatment to investigate the effects of characteristics of graphitic structures on reactivity. Tetracycline (TC) re
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Wu, Zhiyi, Jiahui Shen, Chaoran Li, et al. "Niche Applications of MXene Materials in Photothermal Catalysis." Chemistry 5, no. 1 (2023): 492–510. http://dx.doi.org/10.3390/chemistry5010036.

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MXene materials have found emerging applications as catalysts for chemical reactions due to their intriguing physical and chemical applications. In particular, their broad light response and strong photothermal conversion capabilities are likely to render MXenes promising candidates for photothermal catalysis, which is drawing increasing attention in both academic research and industrial applications. MXenes are likely to satisfy all three criteria of a desirable photothermal catalyst: strong light absorption, effective heat management, and versatile surface reactivity. However, their specific
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Herrero, Enrique, Pepe Jordá-Faus, Rubén Rizo, and Rosa Aran-Ais. "(Invited) Understanding the Oxygen Reduction Reaction on PtPd Single-Crystal Electrodes: The Role of Surface Structure and Composition." ECS Meeting Abstracts MA2025-01, no. 55 (2025): 2666. https://doi.org/10.1149/ma2025-01552666mtgabs.

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The oxygen reduction reaction (ORR) is critical for energy conversion technologies, and its efficiency depends strongly on the electrocatalyst's surface structure and composition. In this study, well-defined PtPd single-crystal electrodes were employed to investigate the influence of surface orientation and Pd incorporation on ORR catalysis in both HClO4 (acidic) and NaOH (alkaline) solutions. Voltammetric analysis in the supporting electrolyte revealed that the addition of Pd alters the adsorption strength of hydroxyl (OH) species, with this effect varying depending on the surface orientation
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Derouane, EricG. "Studies in surface science and catalysis, volume 48 structure and reactivity of surfaces." Journal of Molecular Catalysis 60, no. 1 (1990): 136–37. http://dx.doi.org/10.1016/0304-5102(90)85076-t.

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Trudeau, M. L., and J. Y. Ying. "Nanocrystalline materials in catalysis and electrocatalysis: Structure tailoring and surface reactivity." Nanostructured Materials 7, no. 1-2 (1996): 245–58. http://dx.doi.org/10.1016/0965-9773(95)00308-8.

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Morankar, Ankita, Siddharth Deshpande, Gaurav Deshmukh, Pushkar Ghanekar, Zhenhua Zeng, and Jeffrey Greeley. "(Invited) First Principles Treatments of Heterogeneous Electrocatalysis – Reactivity Trends and Electrocatalyst Structure." ECS Meeting Abstracts MA2024-01, no. 45 (2024): 2553. http://dx.doi.org/10.1149/ma2024-01452553mtgabs.

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Advances in the theoretical understanding of electrochemical systems have, over the past decade, led to growing use of periodic Density Functional Theory studies to treat a surprisingly large ensemble of electrocatalytic reactions, ranging from carbon dioxide electroreduction to oxygen evolution. Many such studies have employed simplified models of the electrochemical environment to determine reactivity trends across a broad space of catalytic materials, while other efforts have focused on developing detailed descriptions of electrochemical phenomena, such as the structure of electrochemical d
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Légaré, Pierre, Gabriela F. Cabeza, and Norberto J. Castellani. "Atomic and electronic structure dependence of surface chemical reactivity." Catalysis Today 89, no. 3 (2004): 363–68. http://dx.doi.org/10.1016/j.cattod.2003.12.009.

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Šutka, Anna, Andris Šutka, Mārtiņš Vanags, et al. "Identifying Iron-Bearing Nanoparticle Precursor for Thermal Transformation into the Highly Active Hematite Photo-Fenton Catalyst." Catalysts 10, no. 7 (2020): 778. http://dx.doi.org/10.3390/catal10070778.

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The hematite photo-Fenton catalysis has attracted increasing attention because it offers strong oxidation of organic pollutants under visible light at neutral pH. In the present work, aqueous synthesis of hematite photo-Fenton catalysts with high activity is demonstrated. We compare photo-Fenton activity for hematite obtained by hydrolyzation at 60 °C or by a thermally induced transformation from iron-bearing nanoparticles, such as amorphous iron oxyhydroxide or goethite. A link between their structure and visible light photo-Fenton reactivity is established. The highest activity was observed
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Sun, Qian, Chun Zeng, Meng-Meng Xing, et al. "Efficiently Engineering Cu-Based Oxide by Surface Embedding of Ce for Selective Catalytic Reduction of NO with NH3." Nano 14, no. 06 (2019): 1950079. http://dx.doi.org/10.1142/s1793292019500796.

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Deliberately engineering oxide composites on constructing and manipulating interactive structures particularly in surface layers was highly desirable for heterogeneous catalysis. Herein, upon the redox replacement reaction between Ce(IV) precursor (Ce(NO[Formula: see text] and Cu2O nano-substrate, an attempt to directly engineer the surface structure of Cu-based substrate was performed by the Ce(IV)–Cu2O etching-embedding process, then the obtained powders were thermo-treated to get a series of Ce–O–Cu catalysts with different Ce:Cu molar ratios for NH3 selective catalytic reduction (NH3-SCR)
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Dissertations / Theses on the topic "Surface structure, reactivity and catalysis"

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Fourre, Elodie. "Surface science and catalysis studies of the structure and reactivity of model catalysts." Thesis, Cardiff University, 2006. http://orca.cf.ac.uk/56085/.

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In this thesis, the structure and reactivity of palladium on titania has been studied on high surface area powdered materials and on low surface area models. Mathematical models have been established which relate the particle radius to various parameters such as particle surface area, density of particles, interparticle distance and coverage. The sintering process is studied through STM imaging and particle size distribution (PSD) calculation on two models. The technique resulting in PSD consists in the calculation of the particle density as a function of 4 parameters: perimeter, area, height
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Jacobs, Luc. "On the importance of the structure and composition in the catalytic reactivity of Au-Ag catalysts." Doctoral thesis, Universite Libre de Bruxelles, 2021. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/325803.

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Au-based catalysts present excellent low temperature activity and selectivity for partial oxidation reactions, but the fundamental issue of atomic oxygen availability, the key parameter to obtain such reactivity, remains present. To enable the O2 dissociation reaction, Au nanoparticles must be smaller than 5 nm, which induces structural issues for upscaled applications. Alloying Au creates synergistic catalytic effects, and this option is investigated here: using residual amounts of Ag enables the O2 dissociation, regardless of the size of the Au-Ag catalyst. Questions remain about the precise
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Newton, Mark A. "Alloy effects in catalysis : the structure and reactivity of the CuPd[85:15]{110}p(2x1) surface." Thesis, University of Liverpool, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240235.

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Stone, Peter John. "STM studies of the structure and reactivity of oxide surfaces and model catalysts." Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340075.

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Miró, Ramírez Pere. "Giant polyoxometalates : dynamic structure and reactivity." Doctoral thesis, Universitat Rovira i Virgili, 2010. http://hdl.handle.net/10803/9104.

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Giant Polyoxometalates : Dynamic Structure and Reactivity. <br/><br/>In this thesis different methods were used to study several systems in which giant polyoxometalates are involved. The validity of the theoretical methods applied and the results obtained were always contrasted with the experimental evidence provided by the groups of Prof. Achim Müller (Bielefeld) and Prof. Marcella Bonchio (Padova). In certain cases the theoretical results provided an explanation for experimental observations and in other cases they had allowed prediction as main objective.<br/><br/>Chapter IV presents the re
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Hermes, A. C. "Structure and reactivity of transition metal clusters." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:91e9449f-8c1e-4955-8c08-d9f24e5bbe6a.

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A range of computational and experimental techniques have been applied to the study of four metal cluster systems. Decorated rhodium clusters Rh n O m (N 2 O) + ( n = 4 − 8, m = 0 − 2) have been investigated both experimentally by IR-MPD and computationally using DFT. The effect of cluster size as well as oxygen coverage on the spectroscopy of the N 2 O bend are analyzed. The infrared-induced decomposition of N 2 O on Rh n O + m is observed on all cluster sizes, with marked differences as a function of size and oxygen coverage, particularly in the case of Rh 5 (N 2 O) + . The oxidation of CO w
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Grillo, Federico. "Structure and reactivity of model oxides related to automobile exhaust catalysis." Thesis, Cardiff University, 2007. http://orca.cf.ac.uk/56181/.

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In this thesis, different ceria and barium oxide based model systems, related to automobile exhaust catalysis, are studied, with the aim of characterizing their structure and reactivity. Chapter 1 is an introduction to the relevance of surface science studies and its cross links with heterogeneous catalysis. The knowledge of a process at atomic scale, which can ultimately be achieved through surface science, can help to improve the design and performance of a material. A description of the techniques used is presented in Chapter 2. The studies of ceria based systems are described in Chapter 3.
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Önsten, Anneli. "Surface Reactivity and Electronic Structure of Metal Oxides." Doctoral thesis, KTH, Materialfysik, MF, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-33667.

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The foci of this thesis are the metal oxides Cu2O, ZnO and Fe3O4 and their interaction with water and sulfur dioxide (SO2). The intention is to study SO2-induced atmospheric corrosion on a molecular level. All studies are based on photoelectron spectroscopy (PES) and scanning tunneling microscopy (STM) measurements. The band structure of Cu2O in the Γ-M direction has been probed by angle-resolved PES (ARPES). It reveals a more detailed picture of the bulk band structure than earlier data and gives the first experimental evidence of a dispersive hybridized Cu 3d-Cu 4s state. The experimental da
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Satterley, Christopher James. "Thiolates on Gold : Surface Structure, Bonding and Reactivity." Thesis, University of Nottingham, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.519388.

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Lee, Yong-Kul. "Reactivity and Structure of Supported Nickel Phosphides (Ni2P) in Deep Hydrodesulfurization Catalysis." Diss., Virginia Tech, 2004. http://hdl.handle.net/10919/30228.

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This dissertation describes preparation and characterization of Ni2P catalysts and their application in deep hydrodesulfurization (HDS) of a model sulfur compound, 4,6-dimethyldibenzothiophene (4,6-DMDBT), one of the most refractory S-compounds. This topic is of great importance in addressing recently enacted environmental regulations limiting the sulfur content in fuels. The work carried out includes synthesis of Ni2P on different siliceous supports, SiO2, MCM-41, and ultra-stable Y zeolite (USY). It also includes determining the characteristics of the supported Ni2P catalysts with a wide
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Books on the topic "Surface structure, reactivity and catalysis"

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Derouane, Eric G. Zeolite Microporous Solids: Synthesis, Structure, and Reactivity. Springer Netherlands, 1992.

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Claudio, Morterra, Zecchina Adriano 1936-, Costa Giacomo 1922-, and Associazione italiana di chimica fisica., eds. Structure and reactivity of surfaces: Proceedings of a European conference, Trieste, Italy, September 13-16, 1988. Elsevier, 1989.

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T, Andras Maria, Hepp Aloysius F, and United States. National Aeronautics and Space Administration., eds. Reactivity of [pi]-complexes of Ti, V, and Nb towards dithioacetic acid: Synthesis and structure of novel metal sulfur-containing complexes. National Aeronautics and Space Administration, 1990.

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T, Andras Maria, Hepp Aloysius F, and United States. National Aeronautics and Space Administration., eds. Reactivity of [pi]-complexes of Ti, V, and Nb towards dithioacetic acid: Synthesis and structure of novel metal sulfur-containing complexes. National Aeronautics and Space Administration, 1990.

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Wise, Henry. Material concepts in surface reactivity and catalysis. Academic Press, 1990.

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Wise, Henry. Material concepts in surface reactivity and catalysis. Dover Publications, 2001.

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Wise, Henry. Material concepts in surface reactivity and catalysis. Dover Publications, 2001.

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Jacques, Oudar, ed. Material concepts in surface reactivity and catalysis. Academic Press, 1990.

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Dyall, Kenneth G. Theoretical investigation of gas-surface interactions. National Aeronautics and Space Administration, Ames Research Center, 1994.

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M, Lambert R., Pacchioni G. 1954-, North Atlantic Treaty Organization. Scientific Affairs Division., and NATO Advanced Study Institute on Chemisorption and Reactivity on Supported Clusters and Thin Films: Towards an Understanding of Microscopic Processes in Catalysis (1996 : Erice, Italy), eds. Chemisorption and reactivity on supported clusters and thin films: Towards an understanding of microscopic processes in catalysis. Kluwer Academic Publishers, 1997.

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Book chapters on the topic "Surface structure, reactivity and catalysis"

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Gallezot, Pierre. "Low-Nuclearity Metal Clusters: Structure and Reactivity." In Surface Organometallic Chemistry: Molecular Approaches to Surface Catalysis. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-2971-5_7.

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Koel, Bruce E. "Structure, Characterization and Reactivity of Pt–Sn Surface Alloys." In Model Systems in Catalysis. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-98049-2_2.

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Bordes, E. "Surface Reactivity of Oxides." In Elementary Reaction Steps in Heterogeneous Catalysis. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1693-0_9.

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van Santen, R. A. "Quantum Chemistry of Surface Chemical Reactivity." In Fundamental Aspects of Heterogeneous Catalysis Studied by Particle Beams. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-5964-7_9.

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Centi, Gabriele, Fabrizio Cavani, and Ferruccio Trifirò. "Control of the Surface Reactivity of Solid Catalysts." In Selective Oxidation by Heterogeneous Catalysis. Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-4175-2_4.

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Centi, Gabriele, Fabrizio Cavani, and Ferruccio Trifirò. "Control of the Surface Reactivity of Solid Catalysts." In Selective Oxidation by Heterogeneous Catalysis. Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-4175-2_5.

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Borfecchia, Elisa, Luca Braglia, Francesca Bonino, et al. "Probing Structure and Reactivity of Metal Centers in Metal–Organic Frameworks by XAS Techniques." In XAFS Techniques for Catalysts, Nanomaterials, and Surfaces. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43866-5_26.

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Bowker, Michael. "The effect of surface structure on reactivity." In The Basis and Applications of Heterogenuous Catalysis. Oxford University Press, 1998. http://dx.doi.org/10.1093/hesc/9780198559580.003.0002.

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This chapter discusses the effect of the surface structure on reactivity. Since the nature of the surface involved in heterogeneous catalysis is crucial to performance, it is important to consider the structure as a starting point for the discussion of catalytic properties. Generally speaking, surfaces with lower coordination surface atoms have the highest surface free energy, the highest reactivity for adsorption, and the strongest binding for the adsorbate (high adsorption heat). Because the surface is a region of high energy, thermodynamics dictates that there will be a tendency to minimise
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"Studies in Surface Science and Catalysis." In Structure and Reactivity of Surfaces. Elsevier, 1989. http://dx.doi.org/10.1016/s0167-2991(08)60758-2.

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Doi, Y., S. Suzuki, F. Nozawa, K. Soga, and T. Keii. "Structure and Reactivity of “Living” Polypropylene." In Studies in Surface Science and Catalysis. Elsevier, 1986. http://dx.doi.org/10.1016/s0167-2991(09)60331-1.

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Conference papers on the topic "Surface structure, reactivity and catalysis"

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Malatji, Residence, Michel Kalenga, and Kasongo Didier Nyembwe. "A REVIEW ON THE USAGE OF BIOCHAR AS AN ALTERNATIVE REDUCTANT IN THE PYROMETALLURGICAL TREATMENT OF ORES." In 24th SGEM International Multidisciplinary Scientific GeoConference 2024. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024v/4.2/s17.11.

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Carbon emission has increasingly become a topic of the day. Carbothermic reduction processes and energy generating units have for years used generic carbonaceous materials contributing to high carbon pollution. Ongoing investigations are showing good prospects. This paper corroborates a comprehensive review on the potential of biochar as an innovative and sustainable alternative to traditional carbon sources in pyrometallurgical processes, addressing the environmental ithreats caused by fossil fuel use, such as greenhouse gas emissions and global warming, and the urgent need for greener reduct
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Bohnsack, G. "Chemistry of Corrosion Inhibition and Surface Passivation of Mild Steel by Hydrazine in Power Plant Circuits." In CORROSION 1989. NACE International, 1989. https://doi.org/10.5006/c1989-89461.

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Abstract After a brief description of the three-component system iron/water/oxygen, a review is given of the several possibilities which hydrazine has to react in this chemical system. The activation of molecular oxygen is of special significance for the passivation of mild steel. The oxidation of ferrous ions in homogeneous aqueous solution is accelerated in accordance with a model of induced oxidation. Complex formation and catalysis of the SCHIKORR reaction are additional properties of hydrazine in boiler feedwater. Hydrazine influences the structure of iron oxides formed and favors the for
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Michalske, T. A. "Fundamental Studies of Glass Fracture." In CORROSION 1992. NACE International, 1992. https://doi.org/10.5006/c1992-92161.

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Abstract Because glass is a brittle material, its susceptibility to fracture often limits its use in technological applications and is thus a topic of practical concern. A particularly vexing phenomenon known to occur in glass is delayed failure or static fatigue. By studying the effect of controlled amounts of reactive gases on the fracture rate in silica glass, we have developed models for the crack tip chemical reactions that lead to stress corrosion fracture. In this study, the measured rates of reaction on strained silicate model compounds and silica surface defect species are used to dem
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Flounders, Emer C., and Marshall K. Judges. "Corrosion Condition Evaluation of Reinforced Concrete Tanks in the National Aquarium in Baltimore." In CORROSION 1994. NACE International, 1994. https://doi.org/10.5006/c1994-94284.

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Abstract Two oval shaped reinforced concrete tanks built one over the other, exhibited significant concrete damage in addition to cracking. The annular space between the walls of the tanks are filled with man made sea water for marine life habitation. Cracks were observed on the walls and the floor slabs. It was suspected that the cracks may be active and that a change in width would occur over time, allowing access of chloride saturated sea water to the reinforcing steel. A detailed field survey was performed to evaluate the condition of the tanks. Select cracks were monitored to determine wh
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Srinivasan, Sridhar, and Gerrit Buchheim. "High Temperature Corrosion Quantification in Renewable Diesel and Sustainable Aviation Fuel Applications." In MECC 2023. AMPP, 2023. https://doi.org/10.5006/mecc2023-20056.

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Abstract Production of Renewable Diesel (RD) and Sustainable Aviation Fuels (SAF) from biological sources (natural oils) has seen exponential growth in recent years, stemming from worldwide government mandated climate change initiatives alongside the need for carbon capture and sequestration. Significant, rapid investments have occurred in retrofitting / adapting existing refinery hydroprocessing infrastructure to process natural oils or coprocess natural oils blended with crudes to produce RD and SAF. This stems from the fact that natural oils have the hydrocarbon (HC) structures to fit withi
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Srinivasan, Sridhar, Winston Robbins, and Gerrit Buchheim. "Quantifying High Temperature Corrosion in Renewable Diesel and Sustainable Aviation Fuel Production." In CONFERENCE 2023. AMPP, 2023. https://doi.org/10.5006/c2023-19457.

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Abstract Production of Renewable Diesel (RD) and Sustainable Aviation Fuels (SAF) from bio / natural oils has seen tremendous interest and investment in recent years, stemming from worldwide government mandated need to reduce fossil fuel CO2 emissions. Significant, rapid investments have occurred in retrofitting / adapting existing refinery hydroprocessing infrastructure to process natural oils or coprocess natural oils blended with crudes to produce RD and SAF. This stems from the fact that natural oils have the hydrocarbon (HC) structures to fit within the mid-distillate fuel product such as
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Zhu, Xiaoyang. "Laser Probe Of Surface Reaction Dynamics." In Laser Applications to Chemical and Environmental Analysis. Optica Publishing Group, 1998. http://dx.doi.org/10.1364/lacea.1998.ltub.5.

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Understanding surface chemical kinetics is essential to the advancement of the frontiers of many vital technologies, such as semiconductor device fabrication and heterogeneous catalysis. This indisputable driving force, along with the rapid development of a large repertoire of atomic, molecular, and structural sensitive surface probes, has been responsible for the built-up of an immense literature on the chemical pathways and kinetics of a large number of molecules on an equally large number of solid surfaces. A typical example of a surface chemical study may involve the identification of surf
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De Oliveira Vigier, Karine, Christophe Coutanceau, and Steve Baranton. "Electro-oxidation of glycerol and diglycerol in the presence of Pt or Pd-based electrocatalyst follows by the reductive amination of the products obtained." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/olba8004.

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The selective electro-oxidation of bio-based organic molecules such as glycerol, polyglycerols, saccharides and furanic compounds has received particular attention in recent years, due to the high value-added compounds that result and their numerous industrial applications. Electrochemical methods are therefore well suited for the controlled oxidation of small organic molecules in aqueous media. Glycerol valorization through partial oxidation is a good way of obtaining many different molecules with high added value such as glyceric acid, tartronic acid, dihydroxyacetone, glyceraldehyde etc.,
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FREUND, HANS-JOACHIM. "STRUCTURE-REACTIVITY RELATIONS THROUGH CHARGE CONTROL AT THE ATOMIC LEVEL IN HETEROGENEOUS CATALYSIS." In 24th International Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2018. http://dx.doi.org/10.1142/9789813237179_0015.

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Singer, David M., François Farges, and Gordon E. Brown. "Biogenic UO2 — Characterization and Surface Reactivity." In X-RAY ABSORPTION FINE STRUCTURE - XAFS13: 13th International Conference. AIP, 2007. http://dx.doi.org/10.1063/1.2644500.

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Reports on the topic "Surface structure, reactivity and catalysis"

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Leeladee, Pannee. Cooperative small-molecule activation toward sustainable catalysis. Faculty of Science, Chulalongkorn University, 2018. https://doi.org/10.58837/chula.res.2018.47.

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In this research, a series of copper complexes containing polypyridyl ligands were designed to study the influence from ligands, nuclearity, solvents and secondary coordination on reactivity toward small-molecule activation. This structure-reactivity relationship was used in investigation for oxygen reduction reactions (ORR), and applied in detection of ascorbic acid (AsH₂). Firstly, copper (II) complexes containing polypyridyl derivatives ligands (i.e., Cu(dpa), Cu(adpa) and Cu₂ (addpa)) were synthesized and fully characterized by elemental analysis, mass spectrometry and X-ray crystallograph
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Tao, Franklin. Understanding of catalysis on early transition metal oxide-based catalysts through exploration of surface structure and chemistry during catalysis using in-situ approaches. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1331817.

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Chefetz, Benny, Baoshan Xing, and Yona Chen. Interactions of engineered nanoparticles with dissolved organic matter (DOM) and organic contaminants in water. United States Department of Agriculture, 2013. http://dx.doi.org/10.32747/2013.7699863.bard.

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Background: Engineered carbon nanotubes (CNTs) are expected to be increasingly released into the environment with the rapid increase in their production and use. The discharged CNTs may interact with coexisting contaminants and subsequently change environmental behaviors and ecological effects of both the CNTs themselves and the contaminants. Dissolved organic matter (DOM) plays a critical role in the transport of CNTs in the aquatic environment, affecting both CNT's surface properties through adsorption, and its colloidal stability in solution. Therefore, CNT-bound DOM complexes may interact
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