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Journal ArticleDOI

Activation and catalytic transformation of methane under mild conditions

TLDR
In this article , the fundamental understanding of these chemical and catalytic transformations of CH4 under mild conditions has been achieved to some extent, although currently neither a catalyst nor a catalytic process can be used for chemical production at a large scale.
Abstract
In the last few decades, worldwide scientists have been motivated by the promising production of chemicals from the widely existing methane (CH4) under mild conditions for both chemical synthesis with low energy consumption and climate remediation. To achieve this goal, a whole library of catalytic chemistries of transforming CH4 to various products under mild conditions is required to be developed. Worldwide scientists have made significant efforts to reach this goal. These significant efforts have demonstrated the feasibility of oxidation of CH4 to value-added intermediate compounds including but not limited to CH3OH, HCHO, HCOOH, and CH3COOH under mild conditions. The fundamental understanding of these chemical and catalytic transformations of CH4 under mild conditions have been achieved to some extent, although currently neither a catalyst nor a catalytic process can be used for chemical production under mild conditions at a large scale. In the academic community, over ten different reactions have been developed for converting CH4 to different types of oxygenates under mild conditions in terms of a relatively low activation or catalysis temperature. However, there is still a lack of a molecular-level understanding of the activation and catalysis processes performed in extremely complex reaction environments under mild conditions. This article reviewed the fundamental understanding of these activation and catalysis achieved so far. Different oxidative activations of CH4 or catalytic transformations toward chemical production under mild conditions were reviewed in parallel, by which the trend of developing catalysts for a specific reaction was identified and insights into the design of these catalysts were gained. As a whole, this review focused on discussing profound insights gained through endeavors of scientists in this field. It aimed to present a relatively complete picture for the activation and catalytic transformations of CH4 to chemicals under mild conditions. Finally, suggestions of potential explorations for the production of chemicals from CH4 under mild conditions were made. The facing challenges to achieve high yield of ideal products were highlighted and possible solutions to tackle them were briefly proposed.

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Journal ArticleDOI

Singly Dispersed Ir1Ti3 Bimetallic Site for Partial Oxidation of Methane at High Temperature

TL;DR: In this paper , a singly dispersed bimetallic site (SDBM), Ir 1 Ti 3 , formed on TiO 2 support during partial oxidation of methane to produce syngas.
Journal ArticleDOI

Visible‐Light‐Induced, Single‐Metal‐Catalyzed, Directed C−H Functionalization: Metal‐Substrate‐Bound Complexes as Light‐Harvesting Agents

TL;DR: In this article , the photochemical modulation of the reaction mechanism using a single transition metal complex can be used as both the photosensitizer and catalyst to promote C−H bond functionalization.
Journal ArticleDOI

Identifying the Metallic State of Rh Catalyst on Boron Nitride during Partial Oxidation of Methane by Using the Product Molecule as the Infrared Probe

TL;DR: In this paper , a rhodium catalyst on boron nitride (Rh/BN) for the partial oxidation of methane (POM) is reported, with exceptional activity and long-term stability at 600 °C for 230 h.
Journal ArticleDOI

Photocatalytic Chlorination of Methane Using Alkali Chloride Solution

TL;DR: In this paper , a photocatalytic approach was proposed to convert inert methane into methyl chloride over NaTaO3 photocatalyst using an alkali chloride solution as the chlorine source under ambient conditions.
Journal ArticleDOI

Direct photocatalytic conversion of methane to value-added chemicals

Huidong Song, +1 more
- 01 Sep 2022 - 
TL;DR: In this article , the authors present the latest advances in direct photocatalytic conversion of methane to liquid oxygenates and higher hydrocarbons, with an emphasis on the strategies for the rational design of photatalysts to improve the activity and selectivity of the desired products.
References
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Journal ArticleDOI

Activation of c-h bonds by metal complexes

TL;DR: In this article, it was shown that the same alkylhydridoplatinum(IV) complex is the intermediate in the reaction of ethane with platinum(II) σ-complexes.
Journal ArticleDOI

Understanding and exploiting C–H bond activation

TL;DR: The recent development of promising catalytic systems highlights the potential of organometallic chemistry for useful C-H bond activation strategies that will ultimately allow us to exploit Earth's alkane resources more efficiently and cleanly as discussed by the authors.
Journal ArticleDOI

New interpretations of XPS spectra of nickel metal and oxides

TL;DR: In this paper, a scheme for fitting the Ni 2p spectra using multiplet envelopes is proposed, based on charge transfer assignments of the main peak at 854.6 eV and the broad satellite centred at around 861 eV to the cd 9 L and the unscreened cd 8 final state configurations, respectively.
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