Yuanyuan Yue

ORCID: 0000-0002-0385-9131
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About
Contact & Profiles
Research Areas
  • Zeolite Catalysis and Synthesis
  • Catalytic Processes in Materials Science
  • Catalysis and Hydrodesulfurization Studies
  • Mesoporous Materials and Catalysis
  • Catalysis and Oxidation Reactions
  • Nanomaterials for catalytic reactions
  • Catalysis for Biomass Conversion
  • Asymmetric Synthesis and Catalysis
  • Metal-Organic Frameworks: Synthesis and Applications
  • Crystallization and Solubility Studies
  • Axial and Atropisomeric Chirality Synthesis
  • X-ray Diffraction in Crystallography
  • Chemical Synthesis and Characterization
  • Covalent Organic Framework Applications
  • Ammonia Synthesis and Nitrogen Reduction
  • Seismic Waves and Analysis
  • Seismic Imaging and Inversion Techniques
  • Catalytic C–H Functionalization Methods
  • Oxidative Organic Chemistry Reactions
  • Clay minerals and soil interactions
  • Petroleum Processing and Analysis
  • Electrocatalysts for Energy Conversion
  • Food Quality and Safety Studies
  • Chemical Synthesis and Analysis
  • Lignin and Wood Chemistry

Fuzhou University
2016-2024

Henan Normal University
2013-2024

China National Petroleum Corporation (China)
2008-2024

Dongbei University of Finance and Economics
2023

Henan University of Technology
2019

China University of Petroleum, Beijing
2014-2015

Henan Institute of Technology
2015

Beijing University of Technology
2012-2014

Zero to Three
2014

Sichuan University
2005-2007

Catalytic dehydrogenation of propane over a Pt-based catalyst to propylene has received considerable interests in recent years because this route is able provide an economical and efficient way fill the gap between supply demand market. The low dispersion Pt particle at support surface sintering nanoparticles under harsh reaction condition are main challenges practical application catalyst. Herein, highly Pt/Sn-Beta catalysts developed for dehydrogenation, which exhibits high activity,...

10.1021/acscatal.9b03527 article EN ACS Catalysis 2019-12-06

Nanocarbon-supported Pt nanoparticles (NPs) were prepared and tested for the propane dehydrogenation reaction (PDH). The nanocarbon support is composed of a nanodiamond core defective, ultrathin graphene nanoshell (ND@G). Pt/ND@G catalyst experienced slight deactivation during 100 h PDH test, while Pt/Al2O3 showed severe after 20 test. NPs exhibited superior sintering resistance versus that ND@G support. This particular structure allows electrons on defects to transfer NPs, leading strong...

10.1021/acscatal.6b03452 article EN ACS Catalysis 2017-04-06

A series of unmodified bulk Al<sub>2</sub>O<sub>3</sub> materials show an intrinsic activity for selectively catalyzing propane dehydrogenation.

10.1039/d0cy00779j article EN Catalysis Science & Technology 2020-01-01

Abstract Iron-modified ZSM-5 zeolites (FeZSM-5s) have been considered to be a promising catalyst system reduce nitrogen oxide emissions, one of the most important global environmental issues, but their synthesis faces enormous economic and challenges. Herein we report cheap green strategy fabricate hierarchical FeZSM-5 from natural aluminosilicate minerals via nanoscale depolymerization-reorganization method. Our is featured by neither using any aluminum-, silicon-, or iron-containing...

10.1038/srep09270 article EN cc-by Scientific Reports 2015-03-20

This article describes a novel method to dealuminate and realuminate H-beta zeolites as catalysts for removing organic acids from bio-oils <italic>via</italic> their esterification reactions with alcohols.

10.1039/c7ra05298g article EN cc-by-nc RSC Advances 2017-01-01

Life cycle assessment and green metrics were used to comparatively assess the synthesis of zeolites from natural minerals chemicals in which former exhibits a better balance between efficiency environmental impacts than latter.

10.1039/d3gc05146c article EN Green Chemistry 2024-01-01

Sulfated zirconia (SZ) and its modified versions attract great interest in recent years, because of their promising potential n-alkane isomerization. The oxidative protonation routes are active interactional activation over SZ catalysts. bimolecular reaction becomes dominant with increasing the density sites on surface decreasing carbon chain feed. Pentane hexane mainly isomerized by protonated cyclopropane mechanism, while which is thermodynamically unflavored for n-butane deactivation...

10.1002/er.4995 article EN International Journal of Energy Research 2020-01-10
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