Jerónimo Juan-Juan
Research Subjects
Jerónimo Juan-Juan has a total of 27 co-authors. Here are the top co-authors by number of shared publications:
- Maria Carmen Román-Martínez
MCMA Group Department of Inorganic Chemistry and Materials Institute (IUMA) University of Alicante Alicante E‐03080 Spain
4 shared publications - María José Illan Gómez
MCMA Group, Inorganic Chemistry Department, Materials Institute of the University of Alicante (IUMA), Faculty of Sciences, University of Alicante, 03690 Alicante, Spain
4 shared publications - Angel Linares-Solano
Grupo de Materiales Carbonosos y Medioambiente, Dpto. Química Inorgánica, Facultad de Ciencias, Universidad de Alicante, Ap. 99, E-03080 Alicante, Spain
3 shared publications - Diego Cazorla-Amorós
Materials Institute and Inorganic Chemistry Department, University of Alicante, Ap. 99, E-03080 Alicante, Spain
3 shared publications - Ion Such Basáñez
Technical Research Services (SSTTI) University of Alicante Parque Científico 03690 Sant Vicent del Raspeig, Alicante Spain
3 shared publications - Fabián Suárez García
Instituto de Ciencia y Tecnología del Carbono (INCAR-CSIC), C/ Francisco Pintado Fe, 26, 33011 Oviedo, Spain
2 shared publications
Latest Publications
- 1 September 2019
- Published by Elsevier in Surface Science
- Vol. 687, 17-24
Plasmon-driven catalysis of adsorbed p-nitroaniline (PNA) by surface-enhanced Raman scattering (SERS): Platinum versus silver
- 1 September 2019
- Published by Elsevier in Surface Science
- Vol. 687, 17-24
Plasmon-driven catalysis of adsorbed p-nitroaniline (PNA) by surface-enhanced Raman scattering (SERS): Platinum versus silver
- 1 February 2019
- Published by Elsevier in Journal of Archaeological Science: Reports
- Vol. 23, 265-280
Sources of the ochres associated with the Lower Magdalenian “Red Lady” human burial and rock art in El Mirón Cave (Cantabria, Spain)
- 1 February 2019
- Published by Elsevier in Journal of Archaeological Science: Reports
- Vol. 23, 265-280
Sources of the ochres associated with the Lower Magdalenian “Red Lady” human burial and rock art in El Mirón Cave (Cantabria, Spain)
- Open Access
Improved CO Oxidation Activity of 3DOM Pr-Doped Ceria Catalysts: Something Other Than an Ordered Macroporous Structure
It is demonstrated that the synthesis procedure for preparing three-dimensionally ordered macroporous (3DOM) Pr-doped ceria catalysts using a polymethylmethacrylate (PMMA) template not only affects the porous structure, but also the chemistry of the ceria surface. The PMMA template does not affect the crystalline features (type of phases, crystallite size, and cell parameter) of Pr-doped ceria, Ce and Pr location into the particles, and the bulk reduction of the Ce-Pr mixed oxide catalysts. On the contrary, the utilization of the PMMA template improves both the porosity and surface redox properties. 3DOM Ce-Pr mixed oxide catalysts combine micro, meso, and macropores, the most area being in the macropore range, while a reference unshaped catalyst presents poor porosity in all ranges. However, the catalyzed CO oxidation rates do not correlate with the surface area of the catalysts (neither micro nor meso/macro). The Ce-Pr-3DOM catalyst also presents improved surface reducibility with regards to the counterpart reference material prepared without the template, and improved redox behavior under reaction conditions; that is, it has a higher area and this area is reduced and reoxidized more easily. X-ray photoelectron spectroscopy analysis evidences that this is mainly attributed to praseodymium cations, which accomplish redox cycles more easily than cerium cations.
Open AccessImproved CO Oxidation Activity of 3DOM Pr-Doped Ceria Catalysts: Something Other Than an Ordered Macroporous Structure
It is demonstrated that the synthesis procedure for preparing three-dimensionally ordered macroporous (3DOM) Pr-doped ceria catalysts using a polymethylmethacrylate (PMMA) template not only affects the porous structure, but also the chemistry of the ceria surface. The PMMA template does not affect the crystalline features (type of phases, crystallite size, and cell parameter) of Pr-doped ceria, Ce and Pr location into the particles, and the bulk reduction of the Ce-Pr mixed oxide catalysts. On the contrary, the utilization of the PMMA template improves both the porosity and surface redox properties. 3DOM Ce-Pr mixed oxide catalysts combine micro, meso, and macropores, the most area being in the macropore range, while a reference unshaped catalyst presents poor porosity in all ranges. However, the catalyzed CO oxidation rates do not correlate with the surface area of the catalysts (neither micro nor meso/macro). The Ce-Pr-3DOM catalyst also presents improved surface reducibility with regards to the counterpart reference material prepared without the template, and improved redox behavior under reaction conditions; that is, it has a higher area and this area is reduced and reoxidized more easily. X-ray photoelectron spectroscopy analysis evidences that this is mainly attributed to praseodymium cations, which accomplish redox cycles more easily than cerium cations.
- 1 June 2016
- Published by Elsevier in Journal of Catalysis
- Vol. 338, 154-167
One step-synthesis of highly dispersed iron species into silica for propylene epoxidation with dioxygen
- 1 June 2016
- Published by Elsevier in Journal of Catalysis
- Vol. 338, 154-167
One step-synthesis of highly dispersed iron species into silica for propylene epoxidation with dioxygen
- 1 February 2012
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 37 (3) , 2370-2381
MOF-5 and activated carbons as adsorbents for gas storage
- 1 February 2012
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 37 (3) , 2370-2381
MOF-5 and activated carbons as adsorbents for gas storage
- 1 August 2010
- Published by Elsevier in Chemical Engineering Journal
- Vol. 162 (2) , 599-608
Gas-phase hydrodechlorination of dichloromethane with activated carbon-supported metallic catalysts
- 1 August 2010
- Published by Elsevier in Chemical Engineering Journal
- Vol. 162 (2) , 599-608
Gas-phase hydrodechlorination of dichloromethane with activated carbon-supported metallic catalysts
- 1 December 2009
- Published by Elsevier in Applied Catalysis A: General
- Vol. 371 (1-2) , 54-59
Ni, Co and bimetallic Ni–Co catalysts for the dry reforming of methane
- 1 December 2009
- Published by Elsevier in Applied Catalysis A: General
- Vol. 371 (1-2) , 54-59
Ni, Co and bimetallic Ni–Co catalysts for the dry reforming of methane
- 1 February 2009
- Published by Elsevier in Applied Catalysis A: General
- Vol. 355 (1-2) , 27-32
Nickel catalyst activation in the carbon dioxide reforming of methane
- 1 February 2009
- Published by Elsevier in Applied Catalysis A: General
- Vol. 355 (1-2) , 27-32
Nickel catalyst activation in the carbon dioxide reforming of methane
- 1 February 2006
- Published by Elsevier in Applied Catalysis A: General
- Vol. 301 (1) , 9-15
Effect of potassium content in the activity of K-promoted Ni/Al2O3 catalysts for the dry reforming of methane
- 1 February 2006
- Published by Elsevier in Applied Catalysis A: General
- Vol. 301 (1) , 9-15
Effect of potassium content in the activity of K-promoted Ni/Al2O3 catalysts for the dry reforming of methane