Academic literature on the topic 'Novel Catalysis'

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Journal articles on the topic "Novel Catalysis"

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Gai, P. L., K. Kourtakis, H. Dindi, and S. Ziemecki. "Novel Xerogel Catalyst Materials for Hydrogenation Reactions and the Role of Atomic Scale Interfaces." Microscopy and Microanalysis 5, S2 (1999): 704–5. http://dx.doi.org/10.1017/s1431927600016846.

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We are developing a new family of heterogeneous catalysts for hydrogenation catalysis. Catalyst synthesis is accomplished using colloidal polymerization chemistry which produce high surface area xerogel catalysts. These xerogels have been synthesized by one-step sol gel chemistry. These catalysts contain ruthenium and modifiers such as gold occluded or incorporated in a titanium oxide matrix. The materials, especially the modified systems exhibit favorable performance in microreactor evaluations for hydrogenation reactions and exhibit high activities. Nanostructural studies have revealed that
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Wan, Qiang, Sen Lin, and Hua Guo. "Frustrated Lewis Pairs in Heterogeneous Catalysis: Theoretical Insights." Molecules 27, no. 12 (2022): 3734. http://dx.doi.org/10.3390/molecules27123734.

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Frustrated Lewis pair (FLP) catalysts have attracted much recent interest because of their exceptional ability to activate small molecules in homogeneous catalysis. In the past ten years, this unique catalysis concept has been extended to heterogeneous catalysis, with much success. Herein, we review the recent theoretical advances in understanding FLP-based heterogeneous catalysis in several applications, including metal oxides, functionalized surfaces, and two-dimensional materials. A better understanding of the details of the catalytic mechanism can help in the experimental design of novel h
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Hamzaoui, Bilel, Anissa Bendjeriou-Sedjerari, Eva Pump, et al. "Atomic-level organization of vicinal acid–base pairs through the chemisorption of aniline and derivatives onto mesoporous SBA15." Chemical Science 7, no. 9 (2016): 6099–105. http://dx.doi.org/10.1039/c6sc01229a.

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Moene, R., M. Makkee, and J. A. Moulijn. "Novel application of catalysis in the synthesis of catalysts." Catalysis Letters 34, no. 3-4 (1995): 285–91. http://dx.doi.org/10.1007/bf00806877.

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Wang, Dabin, Weisong Yu, Bin Jiang, et al. "A Novel Chemiluminescent Method for Efficient Evaluation of Heterogeneous Fenton Catalysts Using Cigarette Tar." Toxics 11, no. 1 (2022): 30. http://dx.doi.org/10.3390/toxics11010030.

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The evaluation of the catalytic capacity of catalysts is indispensable research, as catalytic capacity is a crucial factor to dictate the efficiency of heterogeneous Fenton catalysis. Herein, we obtained cigarette tar-methanol extracts (CTME) by applying methanol to cigarette tar and found that CTME could cause CL reactions with Fe2+/H2O2 systems in acidic, neutral, and alkaline media. The CL spectrum experiment indicated that the emission wavelengths of the CTME CL reaction with Fe2+/H2O2 systems were about 490 nm, 535 nm, and 590 nm. Quenching experiments confirmed that hydroxyl radicals (•O
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Bridges, Denzel, David Fieser, Jannira J. Santiago, and Anming Hu. "Novel Frontiers in High-Entropy Alloys." Metals 13, no. 7 (2023): 1193. http://dx.doi.org/10.3390/met13071193.

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There is little doubt that there is significant potential for high-entropy alloys (HEAs) in cryogenic and aerospace applications. However, given the immense design space for HEAs, there is much more to be explored. This review will focus on four areas of application for HEAs that receive less attention. These focus areas include joining technologies, HEA nanomaterial synthesis, catalysis, and marine applications. The performance of HEAs as a filler metal for welding and brazing as well as their performance as a welded/brazed base metal will be discussed. Various methods for synthesizing HEA na
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Ranocchiari, Marco, Christian Lothschütz, Daniel Grolimund, and Jeroen Anton van Bokhoven. "Single-atom active sites on metal-organic frameworks." Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 468, no. 2143 (2012): 1985–99. http://dx.doi.org/10.1098/rspa.2012.0078.

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Single-site heterogeneous catalysis has been recently accepted as a novel branch of heterogeneous catalysis. Catalysts with single-atom active sites (SAHCs) allow the design and fine-tuning of the active moiety, and can potentially combine the advantages of heterogeneous and homogeneous catalysis. This study illustrates how porous metal-organic frameworks (MOFs) can be synthesized with homogeneous distribution of SAHCs. The catalytic potential of MIXMOFs is shown. A short overview of catalysis with mesoporous silica materials is described to demonstrate their importance in SAHC.
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Zheng, Yidan, Tianze Liu, Jingyou Tai, and Ning Ma. "Recent Advances in Carbon-Based Catalysts for Heterogeneous Asymmetric Catalysis." Molecules 30, no. 12 (2025): 2643. https://doi.org/10.3390/molecules30122643.

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Carbon materials, including graphene, carbon nanotubes, and fullerenes, serve as effective supports for catalysts and play a pivotal role in heterogeneous asymmetric catalysis due to their unique properties and ability to create defined environments for catalytic reactions. Recent research has focused on developing novel carbon-based catalysts that combine the advantages of heterogeneous catalysis with enhanced stability and reusability. This review highlights the synthesis and catalytic applications of graphene, carbon nanotubes, and fullerenes as heterogeneous support materials in asymmetric
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Li, Yong Xiu, Chang Yong Sun, Chang Jiang Yu, Chao Xian Wang, Yun Jun Liu, and Ying Bing Song. "Graphene Oxide and its Applications in Catalysis." Advanced Materials Research 476-478 (February 2012): 1488–95. http://dx.doi.org/10.4028/www.scientific.net/amr.476-478.1488.

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Graphene, a two-dimensional carbon material, has attracted tremendous research interest in recent years due to its exceptional properties, such as excellent electrical, mechanical and thermal properties. Meanwhile, various kinds of novel functional materials based on Graphene oxide are employed in different fields like solar cell, sensor and catalysis. With the increasing number of catalysts during synthesizing graphene-based composites, the development of catalysis science and technology will surely be promoted. This paper reviews recent advances in the preparation and structure of graphene o
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Zhong, Chenglin, Qingwen Zhou, Shengwen Li, et al. "Enhanced synergistic catalysis by a novel triple-phase interface design of NiO/Ru@Ni for the hydrogen evolution reaction." Journal of Materials Chemistry A 7, no. 5 (2019): 2344–50. http://dx.doi.org/10.1039/c8ta11171e.

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High-efficiency synergistic catalysis was realized by a novel triple-phase interface design of the bifunctional catalysts of NiO and Ru nanoparticles, leading to simultaneous enhancement of all elementary steps.
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Dissertations / Theses on the topic "Novel Catalysis"

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Browne, Danielle M. "Novel selenium catalysis." Thesis, Cardiff University, 2008. http://orca.cf.ac.uk/54706/.

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This thesis describes work carried out on catalytic selenium reagents in a range of organic transformations. Four different areas have been investigated and are reported herein. Chapter 2 reports the unsuccessful development into prochiral ligands, where three different chalcogen atoms are incorporated into either a trisubstituted structure or into a crown ether ring. Then reports how these structures could attach to a metal atom and become chiral. A SSe I SeR Chapter 3 describes a range of selenium-based ligands, which has been used in the palladium allylic substitution reaction to see if the
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Neate, Peter Gregory Nigel. "Pathways to sustainable catalysis : from novel catalysts to mechanistic understanding." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/25441.

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Catalysis allows for the controlled formation of new bonds, whilst reducing both time and energy expenditure in the process. Catalysis has traditionally been the realm of precious metals, which have been used to carry out a bewildering array of reactions. However, there is an ever-increasing drive for the development of catalytic methodology employing sustainable and environmentally benign catalysts. Two such candidates are organocatalysis, omitting the need for metals where possible, or the use of iron catalysis. Two key areas to the advancement of the of field catalysis are the identificatio
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Mbuvi, Harun M. "Novel catalysis by metalloporphyrins." [Ames, Iowa : Iowa State University], 2007.

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Trant, Aoife Geraldine. "Structural and catalytic studies of novel Au/Ni enantioselective catalysts." Thesis, St Andrews, 2008. http://hdl.handle.net/10023/854.

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Paliga, James Francis. "Developing Earth-abundant metal-catalysts for hydrofunctionalisation." Thesis, University of Edinburgh, 2018. http://hdl.handle.net/1842/31115.

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The iron-catalysed hydromagnesiation of styrene derivatives has been developed further from previous publications, expanding the electrophile scope to enable the regioselective formation of new carbon-carbon and carbon-heteroatom bonds (Scheme A1). A commercially available pre-catalyst and ligand were used to give an operationally simple procedure that did not require prior synthesis of a catalyst. This work also investigated the hydromagnesiation of dienes, using a screen of ligands commonly used in transition metal catalysis. An investigation into the magnesium-catalysed hydroboration of ole
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Burton, Aaron Steven. "Characterization of Novel Functions and Topologies in RNA." PDXScholar, 2010. https://pdxscholar.library.pdx.edu/open_access_etds/363.

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The RNA World hypothesis describes a period of time during the origins of life in which RNA molecules performed all catalysis and were the only form of information storage. A great deal of evidence has been obtained in support of this hypothesis, however a few key demonstrations are lacking. The first demonstration is of a molecule capable of self-replication that could have plausibly arisen from the prebiotic soup. Previously in the Lehman Laboratory, a 198-nucleotide RNA was discovered that could be fragmented into as many as four pieces ranging from 39 - 63 nucleotides in length. When these
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Ucyigit, Asli Cemil. "Novel triphosphine ligands for carbonylation catalysis." Thesis, University of Bristol, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.406955.

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Frost, Christopher Gregory. "Novel enantiopure ligands for asymmetric catalysis." Thesis, Loughborough University, 1994. https://dspace.lboro.ac.uk/2134/33263.

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The scope of the palladium catalysed allylic substitution reaction is reviewed with particular reference to stereocontrol. The use of enantiopure oxazolines and acetals in asymmetric synthesis is briefly outlined. The work presented is concerned with the design and construction of enantiopure ligands which are able to impart very high levels of enantioselectivity in the aforementioned palladium-catalysed allylic substitution reaction. The ligands exploit the stereochemistry-controlling properties of the oxazoline moiety, whilst incorporating a secondary donor atom. The ligands rely upon an ele
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Clarke, Matthew Lee. "Asymmetric catalysis using novel platinum complexes." Thesis, University of Bath, 1999. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299846.

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Kim, Kyungduk. "Novel Nanocatalyst for the Selective Hydrogenation of Bio-Oil Model Compounds." Thesis, The University of Sydney, 2016. http://hdl.handle.net/2123/16353.

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This thesis focuses on the understanding the effect of various factors, such as physical structures of metal particles, chemical composition of supports and metal-support interactions, on the catalytic performance of Pd or Pt nanocatalysts for hydrodeoxygenation (HDO) of bio-oil model compounds. The first part of the thesis addressed the alternative catalyst synthesis strategy based on emerging double-flame spray pyrolysis method (FSP), which was able to tune the catalytic properties of nanocatalysts without changing their precursors and chemical compositions during the synthesis. A series o
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Books on the topic "Novel Catalysis"

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Baker, R. T. K., 1938-, Murrell Larry L. 1942-, American Chemical Society Meeting, American Chemical Society. Division of Colloid and Surface Chemistry., and Symposium on New Catalytic Materials and Techniques (1989 : Miami Beach, Fla.), eds. Novel materials in heterogeneous catalysis. American Chemical Society, 1990.

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Baker, R. Terry K., and Larry L. Murrell, eds. Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.

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Shirran, Colette. Novel sulfur ligands for palladium catalysis. University College Dublin, 1998.

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Cybulski, Andrzej, Jacob A. Moulijn, and Andrzej Stankiewicz, eds. Novel Concepts in Catalysis and Chemical Reactors. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527630882.

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Bravo-Suárez, Juan J., Michelle K. Kidder, and Viviane Schwartz, eds. Novel Materials for Catalysis and Fuels Processing. American Chemical Society, 2013. http://dx.doi.org/10.1021/bk-2013-1132.

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Lakes, Aisling M. Novel diamine and phosphinamine ligands and their application in asymmetric catalysis. University College Dublin, 1997.

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Moulijn, Jacob A., Andrzej Cybulski, and Andrzej I. Stankiewicz. Novel concepts in catalysis and chemical reactors: Improving the efficiency for the future. Wiley-VCH, 2010.

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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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Philippou, A. Solid state NMR studies of zeolite catalysis and investigation of novel microporous titanosilicates. UMIST, 1995.

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Book chapters on the topic "Novel Catalysis"

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Wolf, E. E., A. Kumar, and A. S. Mukasyan. "Combustion synthesis: a novel method of catalyst preparation." In Catalysis. Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788016971-00297.

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Dumesic, J. A., and W. S. Millman. "Redox Catalysis in Zeolites." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch006.

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Khan, N. A., J. R. Kitchin, V. Schwartz, L. E. Murillo, K. M. Bulanin, and J. G. Chen. "Novel Catalytic Properties of Bimetallic Surface Nanostructures." In Nanotechnology in Catalysis. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9048-8_2.

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Ghaida, Fatima Abi, Sébastien Clément, and Ahmad Mehdi. "Heterogenized Catalysis on Metals Impregnated Mesoporous Silica." In Novel Nanoscale Hybrid Materials. John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119156253.ch10.

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Utz, Bruce R., Anthony V. Cugini, and Elizabeth A. Frommell. "Dispersed-Phase Catalysis in Coal Liquefaction." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch027.

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Dosch, Robert G., Frances V. Stohl, and James T. Richardson. "Hydrous Titanium Oxide-Supported Catalysts." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch026.

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Scaife, Charles W. J., S. Richard Cavoli, and Steven L. Suib. "Crystallization in Space." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch001.

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Zones, Stacy I., and Robert A. Van Nordstrand. "Templates in the Transformation of Zeolites to Organozeolites." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch002.

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Newsam, J. M., T. O. Brun, F. Trouw, L. E. Iton, and L. A. Curtiss. "Inelastic Neutron Scattering from Non-Framework Species Within Zeolites." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch003.

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Cox, David F., and Mark E. Davis. "Silicoaluminophosphate Molecular Sieves." In Novel Materials in Heterogeneous Catalysis. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0437.ch004.

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Conference papers on the topic "Novel Catalysis"

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Mih�ly, Norbert B., Miruna Prodan, Vasile M. Cristea, and Anton A. Kiss. "Sustainable Downstream Process Design for HMF Conversion to Value-Added Chemicals." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.185398.

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Biomass conversion to chemical derivatives and essential intermediates is regarded as a long-term strategy for the chemical sector. Among the numerous valuable chemicals obtained from biomass, 5-hydroxymethylfurfural (HMF) is considered an industrially relevant compound due to its capacity to be converted into a variety of value-added chemicals. Compared to conventional catalytic synthesis, bio-catalysis has emerged as a potential greener substitute for HMF conversion to value-added compounds. HMF conversion through bio-catalysis, although more sustainable, seldom leads to the production of a
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Markova, Mariia, Antonina Stepacheva, Vladimir Molchanov, Galina Demidenko, and Mikhail Sulman. "FISCHER-TROPSCH SYNTHESIS OVER POLYMER SUPPORTED PROMOTED IRON CATALYSTS." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s17.12.

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In recent decades, the interest of researchers has focused on the development of methods for obtaining alternative energy sources. Fischer-Tropsch synthesis is one of the methods for obtaining a wide range of hydrocarbons and their derivatives. Ru, Ni, Fe and Co are the widely used catalytically active metals in FTS. To increase the activity of the catalyst, as well as increase the yield of target products, promoters are introduced into catalytic systems. In FTS, oxides of alkaline and rare earth metals, oxides of lanthanides and actinides, and noble metals are used as modifiers. In this work,
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Shin, Junyoung, Scott Kovaleski, Matthew Maschmann, Connor Gunter, and Marshall Lindsay. "Precise 3D CNT array catalyst patterning using two-photon lithography for enhanced liftoff and scalability." In Novel Patterning Technologies 2025, edited by Richard A. Farrell and Ricardo Ruiz. SPIE, 2025. https://doi.org/10.1117/12.3051129.

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Stepacheva, Antonina, Mariia Markova, Oleg Manaenkov, Elena Shimanskaya, and Valentina Matveeva. "SAWDUST LIQUIEFACTION OVER SCHUNGITE-BASED CATALYST." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s17.26.

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The deep processing of lignocellulose feedstock (including waste from the woodworking industry, agriculture, and agro-industry) allowing the high-added value products to be obtained is one of the key scientific problems. Lignocellulose biomass is a potential feedstock for the production of heat, electricity, fuel, chemicals, and other bioderived products. The liquefaction is considered to be one of the most promising ways to convert lignocellulose biomass into liquid fuels. During the liquefaction, lignocellulose biomass can be efficiently converted into important base compounds, such as furfu
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Hosono, Hideo. "Novel oxide semiconductors for OLEDs and catalysis." In 2016 Compound Semiconductor Week (CSW) [Includes 28th International Conference on Indium Phosphide & Related Materials (IPRM) & 43rd International Symposium on Compound Semiconductors (ISCS)]. IEEE, 2016. http://dx.doi.org/10.1109/iciprm.2016.7528725.

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Medeiros, Antonia Carlene R. F., Alice Maria R. Bernardino, Marcos C. de Souza, and Fernando L. Ortiz. "Synthesis of novel phosphinamide phosphoramidate conjugates with possible applications in catalysis." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819201137.

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Peng, Kai. "SUPERHYDROPHILIC, SUPERAEROPHOBIC NIFE-LDH@NI95CU5 ELECTRODE FOR EFFICIENT OER CATALYSIS." In Pure & Applied Sciences International Conference, 08-09 July 2025, Singapore. Global Research & Development Services Publishing, 2025. https://doi.org/10.20319/mijst.2025.2728.

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Water splitting is a promising technique to produce green hydrogen, but it is severely limited by the sluggish kinetics of the oxygen evolution reaction (OER). Addressing this issue demands not only efficient OER catalysts but also better electrode structure which can guarantee effective and stable utilization of the catalysts. Superhydrophilic/superaerophobic porous structure is an ideal candidate for gas evolution reactions. However, fabricating such electrodes usually involves complex procedures and harsh conditions. Moreover, the effects of porous structure on electrode hydrophilicity, aer
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Huang, B. R., S. M. Wang, C. H. Chen, et al. "The novel method to improve electrical characteristics of p-GaN by using Ni catalysis." In 2004 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2004. http://dx.doi.org/10.7567/ssdm.2004.d-10-2.

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Yang, Hung-Ming, and Wei-Ming Chu. "Ultrasound-Assisted Phase-Transfer Catalysis: Green Synthesis of Substituted Benzoate with Novel Dual-Site Phase-Transfer Catalyst in Solid-Liquid System." In 14th Asia Pacific Confederation of Chemical Engineering Congress. Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-1445-1_210.

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Carey, P. C. "Studies of enzymes by resonance Raman spectroscopy." In International Laser Science Conference. Optica Publishing Group, 1986. http://dx.doi.org/10.1364/ils.1986.thg3.

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By creating a resonance Raman probe in the active site of an enzyme, it is possible to obtain the vibrational spectrum associated with those bonds undergoing catalytic transformation. The approach involves reacting thionoesters RC(= S)OCH3 with a class of enzymes known as cysteine proteases which have an essential SH group in their active sights HS-enzyme. The reaction produces an intermediate RC(= S) S-enzyme which is a dithioester with a λmax near 315 nm. The 324-nm excited RR spectra of the dithioester provide a wealth of detail on the substrate during catalysis; the confirmation of the sub
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Reports on the topic "Novel Catalysis"

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Thayumanavan, Sankaran. A Novel Dendrimer Design for Phase Transfer Catalysis in the Fluorophase. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada433715.

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Pfefferle, Lisa D., and Gary L. Haller. Novel Reforming Catalysts. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1053078.

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Ikura, M., M. Stanciulescu, and J. F. Kelly. Development of novel microemulsion catalysts. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1992. http://dx.doi.org/10.4095/304541.

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Gu, Tianbao, Samuel Simon Araya, and Vincenzo Liso. CFD Modeling of NH3 Synthesis on Ru-Based Catalyst for Hydrogen Storage and Transport. Aalborg University, 2024. https://doi.org/10.54337/aau772652211.

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Hydrogen is often considered as a promising alternative to fossil fuels, however its low boiling point and diffusivity cause a huge challenge for storage and transport. Therefore an alternative fuel like ammonia, containing 17 wt.% hydrogen with a higher boiling point, seems a very promising solution for hydrogen storage and transport. In this paper, ammonia synthesis via the most widely used Haber-Bosch process has been investigated. A computational fluid dynamics (CFD) model is developed for a lab-scale reactor, incorporating the modified Temkin kinetic model describing the complex catalytic
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Stuart Nemser, PhD. Novel Catalytic Membrane Reactors. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/1063626.

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Stair, Peter C. Synthesis and Understanding of Novel Catalysts. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1087079.

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Haynes, H. W. Jr. Novel supports for coal liquefaction catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5252950.

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Haynes, Jr ,. H. W. Novel supports for coal liquefaction catalysts. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/5142662.

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Haynes, H. W. Jr. Novel supports for coal liquefaction catalysts. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6540332.

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Haynes, H. W. Jr. Novel supports for coal liquefaction catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10133264.

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