Results 41 to 50 of about 83,093,681 (218)
Conversion of Stearic Acid into Bio-Gasoline over Pd/ZSM-5 Catalysts with Enhanced Accessibility
Palladium supported on nanocrystalline ZSM-5 (n-ZSM-5, Si/Al = 32) and hierarchical ZSM-5 (h-ZSM-5) with different acidity (Si/Al = 33, 51, 122) were tested in the liquid-phase conversion of stearic acid under nitrogen atmosphere (6 bar).
Marta Arroyo +3 more
doaj +1 more source
Abstract This work studies the combined effect of increasing the post‐reformer temperature and introducing red mud as a support catalyst in the thermocatalytic reforming (TCR®) of digestate. The TCR® method, developed by the Fraunhofer Institute for Environmental, Safety and Energy Technology UMSICHT (abbreviated as Fraunhofer UMSICHT), is an extension
Hillary Onyishi +4 more
wiley +1 more source
Dimerization of naphtha-range Fischer-Tropsch olefins into diesel-range products over zeolite H-ZSM-5 and amorphous silica-alumina [PDF]
Includes abstract.Includes bibliographical references.In this study, the dimerization of 1-hexene and 1-octene (as model compounds for Fischer-Tropsch naphtha-range olefins) into diesel-range olefins was carried out in a tubular, continuous flow fixed ...
Maselosne, Molladi Andrew
core +1 more source
Abstract Energy security and sustainability drive the exploration of innovative conversion strategies for abundant biomass waste into energy‐dense products (solid, liquid, and gaseous biofuels). This study demonstrated the catalytic potential of a coal fly ash (CFA)‐derived ZSM‐5 zeolite in enhancing biomass pyrolysis, focusing on lignocellulosic ...
Januario Da Costa Hossi, Kevin Harding
wiley +1 more source
This review summarizes recent advances in Zn/ZSM‐5 catalysts for propane dehydroaromatization, focusing on active site engineering, co‐aromatization systems, morphological regulation, and machine learning‐guided development. ABSTRACT Propane dehydroaromatization (PDA) represents a promising route for the value‐added utilization of shale gas resources ...
Shijie Zhao +9 more
wiley +1 more source
Fe3Cu1/C (CuFe5O8) was synthesized by high‐temperature carbonization of FexCuyBDC MOF, which exhibited excellent catalytic performance for methane selective oxidation at 80°C. The synergistic effect between Cu and Fe in the derived Fe3Cu1/C (CuFe5O8) composite oxide inhibits deep oxidation compare to Fe/C (Fe3O4), and the reaction proceeds via a free ...
Jiaxin Cai +7 more
wiley +1 more source
Recent Advances in Ionizing Radiation as a Nonequilibrium Chemical Field for Catalysis
Ionizing radiation acts as a nonequilibrium chemical field that generates reactive species and structural perturbations. These radiation‐induced effects bridge catalytic material construction, including metal loading, framework evolution, defect engineering, and carbon‐network reorganization, with selective transformations such as oxidation, reduction,
Junhua Kuang +8 more
wiley +1 more source
The present review discusses the advancement in the catalytic synthesis of 5‐alkoxymethylfurfural (AMF) and levulinate esters (LEs) from the aspects of catalytic systems, reaction mechanisms, product isolation, and techno‐economic analysis, supplying valuable insights toward future sustainable and efficient manufacture of AMF and LEs. ABSTRACT The huge
Jun Zhang +6 more
wiley +1 more source
An Investigation on the Catalytic Degradation of Dyeing Wastewater with Fe-ZSM-5 Zeolite
A homogeneous ferrous salt catalyst was used in the traditional Fenton oxidation technology for dyeing wastewater. However, it was difficult to avoid the secondary pollution and loss of ferrous ions.
BI Hai-chao +3 more
doaj
Unbiased Reaction Network Exploration of C–C Coupling in Methane Dehydroaromatization Over Mo‐ZSM‐5
Automated reaction route mapping reveals distinct methane coupling pathways over mono‐ and dinuclear Mo carbide species in ZSM‐5. Mononuclear [MoC]2+ selectively forms desorbable C2H4, whereas dinuclear [Mo2C2]2+ promotes strongly adsorbed C3/C4 intermediates linked to coke formation.
Shunsaku Yasumura, Masaru Ogura
wiley +1 more source

