Academic literature on the topic 'Bifunctional catalysis'

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Journal articles on the topic "Bifunctional catalysis"

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Dixon, Darren J. "Bifunctional catalysis." Beilstein Journal of Organic Chemistry 12 (May 25, 2016): 1079–80. http://dx.doi.org/10.3762/bjoc.12.102.

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Elsby, Matthew R., and R. Tom Baker. "Strategies and mechanisms of metal–ligand cooperativity in first-row transition metal complex catalysts." Chemical Society Reviews 49, no. 24 (2020): 8933–87. http://dx.doi.org/10.1039/d0cs00509f.

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Gao, Jing, Dan Ren, Xueyi Guo, Shaik Mohammed Zakeeruddin, and Michael Grätzel. "Sequential catalysis enables enhanced C–C coupling towards multi-carbon alkenes and alcohols in carbon dioxide reduction: a study on bifunctional Cu/Au electrocatalysts." Faraday Discussions 215 (2019): 282–96. http://dx.doi.org/10.1039/c8fd00219c.

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Murzin, D. Yu. "Mesolevel Bifunctional Catalysis." Kinetics and Catalysis 61, no. 1 (2020): 80–92. http://dx.doi.org/10.1134/s0023158420010073.

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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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Tan, Kian, Xixi Sun, and Amanda Worthy. "Scaffolding Catalysis: Expanding the Repertoire of Bifunctional Catalysts." Synlett 23, no. 03 (2012): 321–25. http://dx.doi.org/10.1055/s-0031-1290321.

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Choudhury, Joyanta, and Shrivats Semwal. "Emergence of Stimuli-Controlled Switchable Bifunctional Catalysts." Synlett 29, no. 02 (2017): 141–47. http://dx.doi.org/10.1055/s-0036-1591741.

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Can a single catalyst perform more than one ‘type’ of reaction? If we consider traditional design of catalysts, then the answer would probably be ‘no’. However, with the advancement of catalyst design concepts, chemists have been able to demonstrate the above task, thanks to ‘stimuli-switchable bifunctional catalysts’. Within the nascent research area of ‘artificial switchable catalysis’, this new type of system offers the potential to achieve complex functions which are otherwise difficult or impossible. This Synpacts article highlights the rise of these new-generation catalysts.1 Introductio
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Breslow, Ronald. "Bifunctional binding and catalysis." Supramolecular Chemistry 1, no. 2 (1993): 111–18. http://dx.doi.org/10.1080/10610279308040656.

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KIKUCHI, K., R. HANNAK, M. GUO, A. KIRBY, and D. HILVERT. "Toward bifunctional antibody catalysis." Bioorganic & Medicinal Chemistry 14, no. 18 (2006): 6189–96. http://dx.doi.org/10.1016/j.bmc.2006.05.071.

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Jahan, Maryam, Satoshi Tominaka та Joel Henzie. "Phase pure α-Mn2O3 prisms and their bifunctional electrocatalytic activity in oxygen evolution and reduction reactions". Dalton Transactions 45, № 46 (2016): 18494–501. http://dx.doi.org/10.1039/c6dt03158g.

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Synthesizing manganese oxide nanomaterials with exact control of shape and phase is difficult, making it challenging to understand the influence of the surface structure on catalysis. We show that phase pure bixbyite crystals can function as bifunctional non-precious metal catalysts for OER and ORR.
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Dissertations / Theses on the topic "Bifunctional catalysis"

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Goldys, Anna M. "Immobilisation and application of bifunctional iminophosphorane organocatalysts." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:f4f28a47-0373-4b66-8537-d4e7028d4d63.

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Bifunctional iminophosphoranes, containing a triaryl-substituted iminophosphorane and bis(3,5- trifluoromethyl)phenyl thiourea on a single enantiomer scaffold are novel asymmetric superbase organocatalysts reported by the Dixon group in 2014. This thesis describes our efforts to expand their scope and utility in a variety of challenging chemical transformations. Chapter 2 describes the development and application of immobilised bifunctional iminophosphorane organocatalysts. We have successfully immobilised bifunctional iminophosphoranes on a crosslinked polystyrene support and applied this sol
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Daly, Christopher Gary. "Applications of amido-N-heterocyclic carbene ligands in bifunctional catalysis." Thesis, University of Leicester, 2013. http://hdl.handle.net/2381/27800.

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This thesis describes the synthesis of amino/amido-N-heterocyclic carbene (NHC) complexes of late transition metals, in order to investigate bifunctional catalysis involving a metal-amido bond. Chapter one introduces bifunctional catalysis, with an emphasis on the mechanism of bifunctional bond-breaking during catalytic reactions. Mechanisms of C-H activation are described and the features of bifunctional C-H activation (AMLA) discussed. The ligand properties, and methods of synthesis, of NHC and amido ligands are described, and the choice of ligand to investigate bifunctional catalysis ration
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Yamaguchi, Yukako. "Molecular Design of Bifunctional Amino Sulfonamides for Asymmetric Enamine Catalysis." 京都大学 (Kyoto University), 2009. http://hdl.handle.net/2433/124447.

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Knapp, Spring Melody, and Spring Melody Knapp. "Investigation of Secondary Coordination Sphere Effects for Cyanohydrin Hydration with Transition Metal Catalysts." Thesis, University of Oregon, 2012. http://hdl.handle.net/1794/12362.

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The synthesis of high value acrylic monomers is currently done industrially via cyanohydrin hydration using concentrated acids, resulting in large quantities of useless byproducts. This current process is energy intensive and lacks atom economy; therefore, alternative cyanohydrin hydration strategies are under investigation. Ideally, cyanohydrin hydration would be done using organometallic nitrile hydration catalysts. Cyanohydrin hydration with these catalysts is challenging, because it needs to be done at low temperatures and under acidic conditions to reduce cyanohydrin degradation and catal
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Kinghorn, Michael James. "Bifunctional Helical Peptide Catalysts for Enzyme-like Reactivity and Selectivity and Selective Stapling of Natural Amino Acid Residues with Hydrophilic Squaric Acid Derivatives." BYU ScholarsArchive, 2019. https://scholarsarchive.byu.edu/etd/8714.

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Peptide secondary structure provides an exceptional scaffold on which to design highly reactive and selective enzyme-like catalysts. This work describes the rational design and synthesis of a suite of helical peptide catalysts that are capable of achieving proximity-induced rate enhancement in Diels-Alder cycloadditions and indole alkylations. Microwave assisted synthesis of resin-supported polypeptides enables incorporation of non-natural amino acid residues that induce helicity (Aib) or provide functional handles on which organic catalytic residues can be attached. These small peptide cat
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Fitchett, Brandon. "Oxidation State Roulette:Synthesis and Reactivity of Cobalt Complexes Containing SNS Ligands." Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/38566.

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The use of rare and expensive noble metals in the chemical industry as organometallic catalysts has grown exponentially in the past few decades due to their high activity, selectivity and their ability to catalyze a wide range of reactions. With this growth in use has also come a proportional growth in concern as these toxic metals inevitably leach into the environment and their negative effects on public health and our ecosystems are becoming better understood. First-row transition metal catalysts provide both environmental and economic benefits as alternatives to these noble metals due to th
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Abudawood, Raed Hasan. "Hydroisomerization of alkanes over metal-loaded zeolite catalysts." Thesis, University of Manchester, 2011. https://www.research.manchester.ac.uk/portal/en/theses/hydroisomerization-of-alkanes-over-metalloaded-zeolite-catalysts(4511d50c-ff42-49e6-9a8a-d7ad88576bb1).html.

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Zeolite catalysis plays an important role in many industrial applications due to their unique properties and has become widely used in the area of oil refining. Of particular interest is Zeolite Y, which can be hydrothermally treated into its ultrastable form, USY. USY offers a superior practicality, especially when dealuminated and metal-loaded. The importance of alkanes hydroisomerization arises from the continuingly stricter regulations imposed on the utilization of gasoline as an automotive fuel. The requirements to reduce the aromatics content in gasoline present a need to find an alterna
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Cesari, Cristiana <1988&gt. "Novel Ruthenium Complexes for Bifunctional Catalysis: the Dual Role of Cyclopentadienone and N-Heterocyclic Carbene." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amsdottorato.unibo.it/7525/1/cesari_cristiana_tesi.pdf.

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The PhD thesis herein presented deal with the synthesis, characterization and catalytic application of new ruthenium transition metal complexes which exhibit unprecedented combination of ligands: cyclopentadienones and N-heterocyclic carbenes (NHC). In the first year of the PhD work it was developed a straightforward and efficient synthetic route to novel Ru N-heterocyclic carbenes (NHC) complexes by transmetallation of non-bulky imidazolylidene silver complexes to ruthenium dicarbonyl tetraarylcyclopentadienone. The same procedure with sterically demanding NHC resulted in the formation of unp
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Cesari, Cristiana <1988&gt. "Novel Ruthenium Complexes for Bifunctional Catalysis: the Dual Role of Cyclopentadienone and N-Heterocyclic Carbene." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2016. http://amsdottorato.unibo.it/7525/.

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The PhD thesis herein presented deal with the synthesis, characterization and catalytic application of new ruthenium transition metal complexes which exhibit unprecedented combination of ligands: cyclopentadienones and N-heterocyclic carbenes (NHC). In the first year of the PhD work it was developed a straightforward and efficient synthetic route to novel Ru N-heterocyclic carbenes (NHC) complexes by transmetallation of non-bulky imidazolylidene silver complexes to ruthenium dicarbonyl tetraarylcyclopentadienone. The same procedure with sterically demanding NHC resulted in the formation of unp
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Catherin, Nelly. "Selective ring opening of naphthenes over bifunctional catalysts in the presence of H2S." Thesis, Lyon, 2016. http://www.theses.fr/2016LYSE1246.

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L'ouverture sélective de cycle (OSC) d'hydrocarbures polycycliques vise à augmenter le nombre de cétane des carburants diesel. OSC efficace peut être atteint par l'hydroconversion sur des catalyseurs bifonctionnels métal noble/fonction acide. La décaline et, à plus faible mesure, le perhydroindane, le butylcyclohexane et la tétraline, ont été utilisés comme molécules modèles pour l'étude des l'OSC de sulfures de métaux de transition (TMSs) supportés sur zéolithes ou silice-alumine amorphe dans un réacteur à lit fixe sous haute pression (5 MPa) avec une concentration élevée d'H2S dans la charge
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Books on the topic "Bifunctional catalysis"

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Ikariya, Takao, and Masakatsu Shibasaki, eds. Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-20731-0.

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Ikariya, Takao. Bifunctional Molecular Catalysis. Springer-Verlag Berlin Heidelberg, 2011.

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Horkan, Carlos K. Bifunctional catalysis in organic chemistry. UMIST, 1998.

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Wang, Yan-Jie, Rusheng Yuan, Anna Ignaszak, David P. Wilkinson, and Jiujun Zhang. Advanced Bifunctional Electrochemical Catalysts for Metal-Air Batteries. CRC Press, 2018. http://dx.doi.org/10.1201/9781351170727.

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Fang, Zhen, Richard L. Smith, and Hu Li, eds. Production of Biofuels and Chemicals with Bifunctional Catalysts. Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-5137-1.

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Joseph, Singer, and United States. National Aeronautics and Space Administration., eds. A study of NAxPtO as an O electrode bifunctional electrocatalyst. National Aeronautics and Space Administration, 1991.

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Ikariya, Takao, and Masakatsu Shibasaki. Bifunctional Molecular Catalysis. Springer, 2013.

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Ikariya, Takao, and Masakatsu Shibasaki. Bifunctional Molecular Catalysis. Springer, 2011.

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Lalonde, Mathieu Pascal. Chiral thioureas in asymmetric catalysis: From simple to bifunctional. 2009.

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Nikoshvili, Linda Zh, Lioubov Kiwi-Minsker, and Valentin Yu Doluda, eds. Transition-Metal-Containing Bifunctional Catalysts: Design and Catalytic Applications. MDPI, 2025. https://doi.org/10.3390/books978-3-7258-4073-1.

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Book chapters on the topic "Bifunctional catalysis"

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Shibasaki, Masakatsu, Motomu Kanai, Shigeki Matsunaga, and Naoya Kumagai. "Multimetallic Multifunctional Catalysts for Asymmetric Reactions." In Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_1.

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Ikariya, Takao. "Bifunctional Transition Metal-Based Molecular Catalysts for Asymmetric Syntheses." In Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_2.

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Mizuno, Noritaka, Keigo Kamata, and Kazuya Yamaguchi. "Liquid-Phase Selective Oxidation by Multimetallic Active Sites of Polyoxometalate-Based Molecular Catalysts." In Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_3.

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Li, Pingfan, and Hisashi Yamamoto. "Bifunctional Acid Catalysts for Organic Synthesis." In Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_4.

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Ito, Jun-ichi, and Hisao Nishiyama. "Bifunctional Phebox Complexes for Asymmetric Catalysis." In Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_5.

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Gunanathan, Chidambaram, and David Milstein. "Bond Activation by Metal-Ligand Cooperation: Design of “Green” Catalytic Reactions Based on Aromatization-Dearomatization of Pincer Complexes." In Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_6.

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Warner, Madeleine C., Charles P. Casey, and Jan-E. Bäckvall. "Shvo’s Catalyst in Hydrogen Transfer Reactions." In Bifunctional Molecular Catalysis. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/3418_2011_7.

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Pihko, Petri M., and Hasibur Rahaman. "Bifunctional Acid-Base Catalysis." In Enantioselective Organocatalyzed Reactions I. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3865-4_6.

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Tanabe, Kozo. "Acid-Base Bifunctional Catalysis." In Acidity and Basicity of Solids. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0986-4_16.

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Thybaut, J. W., M. K. Saeys, G. G. Martens, G. B. Marin, P. A. Jacobs, and J. A. Martens. "Hydrocracking on Bifunctional Zeolites: An Integrated Approach." In Combinatorial Catalysis and High Throughput Catalyst Design and Testing. Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4329-5_21.

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Conference papers on the topic "Bifunctional catalysis"

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Falowo, Olayomi Abiodun, Olusegun John Ojediran, Ibukun Joedanace Adedara, Olumuyiwa Moses, and Bamidele Ogunsemi. "Application of Bifunctional Catalyst in Optimization of Transesterification of Delonix Regia Seed Oil via One-pot Production Route." In 2024 International Conference on Science, Engineering and Business for Driving Sustainable Development Goals (SEB4SDG). IEEE, 2024. http://dx.doi.org/10.1109/seb4sdg60871.2024.10630045.

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Neylon, Michael K., Mario J. Castagnola, A. Jeremy Kropf, and Christopher L. Marshall. "Bifunctional Catalysts for the Selective Catalytic Reduction of NO by Hydrocarbons." In ASME 2004 Internal Combustion Engine Division Fall Technical Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/icef2004-0902.

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Novel bifunctional catalysts combining two active phases, typically Cu-ZSM-5 and a modifier, were prepared and tested for the selective catalytic reduction of nitrogen oxides using propylene in order to overcome the hindering effects of water typically seen for single-phase catalysts such as Cu-ZSM-5. The catalysts were made by typical preparation techniques, but parameters could be varied to influence the catalyst. The physical characterization of the materials showed that the modification phase was added strictly to the external surface of the zeolite without hindering any internal surface a
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Palos, Roberto, David Trueba, Francisco J. Vela, José M. Arandes, and Alazne Gutiérrez. "CuO/ZnO/MnO-based bifunctional catalysts for glycerol hydrogenolysis." In 14th Mediterranean Congress of Chemical Engineering (MeCCE14). Grupo Pacífico, 2020. http://dx.doi.org/10.48158/mecce-14.dg.04.02.

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Al. Sofy, Shatha Abd-Alhameed. "Enhanced surface acidity in bifunctional X-zeolite catalysts: FTIR study." In 2ND INTERNATIONAL CONFERENCE ON MATERIALS ENGINEERING & SCIENCE (IConMEAS 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0000442.

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Shkurenok, V. A., M. D. Smolikov, D. I. Kir'yanov, and A. S. Belyi. "Isomerization of alkanes over bifunctional Pt(Pd)/WO3-ZrO2 catalysts." In OIL AND GAS ENGINEERING (OGE-2021). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0075226.

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Marinič, Dana, Brigita Hočevar, Miha Grilc, and Blaž Likozar. "One-pot Algae Conversion Into Sustainable Biofuel by Catalytic Hydroprocessing." In International Conference on Technologies & Business Models for Circular Economy. University of Maribor Press, 2022. http://dx.doi.org/10.18690/um.fkkt.3.2022.2.

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Microalgae have emerged as a promising feedstock for third generation biofuels. This study aims to investigate the reaction conditions for biodiesel production from microalgae. Microalgae were liquefied and transformed into a mixture of diesel like hydrocarbons using commercial bifunctional NiMo/γ-Al2O3 catalyst. GC-MS analysis revealed that the produced bio-oils are a complex mixtures of partially or completely deoxygenated compounds. The most promising experiment using 25 wt% of catalyst at 350 °C of reaction temperature and 50 bar of initial hydrogen pressure yielded 22.6 wt% of liquid alka
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"PRODUCTION OF PROPYLENE CARBONATE FROM CO2 USING BIFUNCTIONAL HALOMETALLATE CATALYSTS [Bu4N]n[MCl4]." In International Symposium on Energy: Energy Transition, Green Hydrogen and Sustainable Industry. Softaliza Tecnologias, 2024. https://doi.org/10.55592/ise.v2i1.11179.

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Mahmud, Nafis, Muhammad Arsalan, Haya N. Al Jehani, Muneer M. Ba-Abbad, and Muftah H. El-Naas. "Bifunctional Cu-Based Catalyst for Electrochemical Conversion of Carbon Dioxide into CO and Formate." In 8th International Conference on Theoretical and Applied Nanoscience and Nanotechnology. Avestia Publishing, 2024. http://dx.doi.org/10.11159/tann24.137.

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Astar, Ismail, Thamrin Usman, Nelly Wahyuni, Rudiyansyah, and Andi Hairil Alimuddin. "Bifunctional heterogeneous catalysts from oil palm empty fruit bunches ash and alum for biodiesel synthesis simultaneously." In PROCEEDINGS FROM THE 14TH INTERNATIONAL SYMPOSIUM ON THERAPEUTIC ULTRASOUND. Author(s), 2017. http://dx.doi.org/10.1063/1.4978177.

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Palomo Nicolau, Claudio, Saioa Diosdado, Julen Etxabe, et al. "Catalytic Enantioselective Synthesis of Tertiary Thiols from 5H-Thiazol-4-ones: Bifunctional Ureidopeptide-Based Brønsted Base Catalyst." In MOL2NET 2016, International Conference on Multidisciplinary Sciences, 2nd edition. MDPI, 2016. http://dx.doi.org/10.3390/mol2net-02-08017.

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Reports on the topic "Bifunctional catalysis"

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Betley, Theodore, M. Lalonde, G. T. Sazama, and A. B. Scharf. Bifunctional Catalysts for CO2 Reduction. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada610432.

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Connor, William. Bifunctional Nanostructured Base Catalysts: Opportunities for BioFuels. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/1129860.

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Dumesic, James. FUNDAMENTAL STUDIES OF BIFUNCTIONAL CATALYSTS FOR TANDEM REACTIONS. Office of Scientific and Technical Information (OSTI), 2022. http://dx.doi.org/10.2172/1906353.

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Klier, K., R. G. Herman, and M. Deemer. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6737408.

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Klier, K., R. G. Herman, and M. Richards-Babb. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7233244.

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Klier, K., R. G. Herman, M. Richards-Babb, and M. Kieke. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5744996.

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Klier, K., and R. G. Herman. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5348544.

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Klier, K., R. G. Herman, and M. Deemer. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/6649378.

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Klier, K., R. G. Herman, and M. Richards-Babb. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Technical progress report, March--May 1992. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10163729.

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Klier, K., R. G. Herman, M. Richards-Babb, and M. Kieke. Ethanol synthesis and water gas shift over bifunctional sulfide catalysts. Technical progress report, September--November 1991. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/10127128.

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