G
Gabriele Centi
Researcher at University of Messina
Publications - 574
Citations - 27331
Gabriele Centi is an academic researcher from University of Messina. The author has contributed to research in topics: Catalysis & Maleic anhydride. The author has an hindex of 77, co-authored 542 publications receiving 23856 citations. Previous affiliations of Gabriele Centi include Tianjin University & United Nations Industrial Development Organization.
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Opportunities and prospects in the chemical recycling of carbon dioxide to fuels
TL;DR: In this paper, the opportunities and prospects in the chemical recycling of carbon dioxide to fuels, as a complementary technology to carbon sequestration and storage (CSS), are analyzed, and it is remarked that the requisites for this objective are (i) minimize as much as possible the consumption of hydrogen (or hydrogen sources), (ii) produce fuels that can be easily stored and transported, and (iii) use renewable energy sources.
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Nanocarbons for the Development of Advanced Catalysts
TL;DR: This poster presents a probabilistic procedure to evaluate the response of the H2O/O2 mixture to various pyrolysis conditions and shows promising results in both the horizontal and the vertical domain.
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Catalysis for CO2 conversion: a key technology for rapid introduction of renewable energy in the value chain of chemical industries
TL;DR: In this article, the authors discuss the routes, opportunities and barriers in increasing the share of renewable energy by using CO2 reaction and their impact on the chemical and energy value chains.
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Mechanistic aspects of maleic anhydride synthesis from C4 hydrocarbons over phosphorus vanadium oxide
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Electrocatalytic Synthesis of Ammonia at Room Temperature and Atmospheric Pressure from Water and Nitrogen on a Carbon-Nanotube-Based Electrocatalyst.
Shiming Chen,Siglinda Perathoner,Claudio Ampelli,Chalachew Mebrahtu,Dangsheng Su,Gabriele Centi +5 more
TL;DR: Data indicate that the active sites in NH3 electrocatalytic synthesis may be associated to specific carbon sites formed at the interface between iron particles and CNT and able to activate N2, making it more reactive towards hydrogenation.