Chemical kinetics is a branch of physical chemistry that analyzes the rate of reaction in each elemental stage as well as the catalytic mechanism that governs it. Molecular reaction dynamics, catalytic dynamics, elemental reaction dynamics, macrodynamics, and microdynamics are mainly included in it. The catalyst volume, surface, or mass can all influence the catalytic reaction rate. Furthermore, rates are frequently denoted as per volume of reactor in practical applications. In heterogeneous catalysis, such a study field has numerous applications. Chemical kinetics has advanced at a breakneck pace in recent years, with the confined fields gradually expanding as the study mode progressed from the basement state to the excitation state, from small molecules to large molecules, and from the gas phase to the condensed phase.
Stanislaw Dzwigaj
Sorbonne University, France
Sergey Suchkov
R&D Director of the National Center for Human Photosynthesis, Mexico
Thomas J J Muller
Heinrich-Heine-Universitat Dusseldorf, Germany
Dai Yeun Jeong
Jeju National University, Korea, Republic of
Ephraim Suhir
Portland State University, United States
Vladimir Valentinovich Egorov
FSRC “Crystallography and Photonics” RAS, Russian Federation
Carlos Fonte
Johnson Matthey Technology Centre, United Kingdom
Junwang Tang
Tsinghua University, ChinaSubmit your abstract Today
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Sergey Suchkov, R&D Director of the National Center for Human Photosynthesis, Mexico
Title : Application of metal single-site zeolite catalysts in heterogeneous catalysis
Stanislaw Dzwigaj, Sorbonne University, France
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Dai Yeun Jeong, Jeju National University, Korea, Republic of
Title : Catalytic one-pot multicomponent syntheses of functional chromophores – Synthetic efficiency meets functionality design
Thomas J J Muller, Heinrich-Heine-Universitat Dusseldorf, Germany
Title : Analytical expressions of substrate concentrations for different particles in an immobilized enzyme system by new method AYM
M R Akbari, Department of Civil Engineering and Chemical Engineering, Germany
Title : From photocatalysis to photon-phonon co-driven catalysis for inert molecules activation
Junwang Tang, Tsinghua University, China