Catalytic Conversion of Light Alkanes

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Catalysis in Organic and Polymer Chemistry".

Deadline for manuscript submissions: closed (10 December 2021) | Viewed by 272

Special Issue Editors


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Guest Editor
Industrial Catalysis, School of Chemical Engineering, Dalian University of Technology, Dalian, China
Interests: Interests: heterogeneous catalysis; catalytic conversion of light alkanes; noble metal catalyst; oxide and nitride catalyst

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Guest Editor
National Engineering Research Center of Chemical Fertilizer Catalyst, School of Chemical Engineering, Fuzhou University, Fuzhou 350002, China
Interests: heterogeneous catalysis; light alkane activation and conversion; zeolite; supported metal catalyst

Special Issue Information

Dear Colleagues,

Catalytic conversions of light alkanes into industrial chemicals, such as olefins, aromatics, oxygenates, and organic nitrides, are promising candidates for traditional petroleum-based or coal-based producing routes. In recent years, research enthusiasm in this field has been reignited by the rapid exploration of shale gas, combustible ice, and deep-water gas, which contain a considerable amount of light alkane resources. The main aim of scientists in this field remains to develop active, selective, and stable catalysts that are economical and environmentally friendly. New chemical-synthesizing strategies, structure-tuning methods, and novel catalyst systems are crucial to that end, but atomic-scale knowledge of catalyst structures and molecule-level understanding of reaction processes must be achieved in order to develop active and stable catalysts. Further advances are expected to combine theoretical simulation, spectroscopic characterization, and dynamic analysis to disclose the reaction mechanism under realistic reaction conditions.

This Special Issue aims to report on recent progress and developments in light-alkane-converting catalysts. It will focus on catalyst synthesis and characterization, as well as research into understanding the reaction mechanism of alkane conversion. We invite the scientific community to contribute original research or review articles that explore light-alkane-converting catalysts to optimize catalytic performance.

Prof. Dr. Lei Shi
Prof. Dr. Haibo Zhu
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Catalysts is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • light alkanes
  • catalyst synthesis
  • catalytic dehydrogenation
  • oxidative dehydrogenation
  • selective oxidation
  • ammoxidation
  • aromatization

Published Papers

There is no accepted submissions to this special issue at this moment.
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