Microbubble-induced oxidation offers an effective approach for activating the C(sp)-H bond of methane under mild conditions, achieving a methane activation rate of up to 6.7% per hour under optimized parameters. In this study, microbubbles provided an extensive gas-liquid interface that promoted the formation of hydroxyl (OH˙) and hydrogen radicals (H˙), which facilitated the activation of methane, leading to the generation of methyl radicals (CH˙). These species further participated in free-radical reactions at the interface, resulting in the production of ethane and formic acid. The microbubble system was optimized by adjusting gas-liquid interaction time, water temperature, and bubble size, with the optimal conditions (150 s of water-gas interaction, 15 °C, 50 μm bubble size) yielding a methane conversion rate of 171.5 ppm h, an ethane production rate of 23.5 ppm h, and a formic acid production rate of 2.3 nM h during 8 h of continuous operation. The stability and efficiency of this process, confirmed through electron spin resonance, high-resolution mass spectrometry, and gas chromatography, suggest that microbubble-based methane activation offers a scalable and energy-efficient pathway for methane utilization.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11446311PMC
http://dx.doi.org/10.1039/d4sc05773bDOI Listing

Publication Analysis

Top Keywords

csp-h bond
8
methane activation
8
formic acid
8
bubble size
8
production rate
8
methane
7
methane csp-h
4
activation
4
bond activation
4
activation water
4

Similar Publications

Palladium Iodide Catalyzed Multicomponent Carbonylative Synthesis of 2-(4-Acylfuran-2-yl)acetamides.

Molecules

September 2023

Laboratory of Industrial and Synthetic Organic Chemistry (LISOC), Department of Chemistry and Chemical Technologies, University of Calabria, Via Pietro Bucci 12/C, 87036 Arcavacata di Rende, Italy.

2-Propargyl-1,3-dicarbonyl compounds have been carbonylated under oxidative conditions and with the catalysis of the PdI/KI catalytic system to selectively afford previously unreported 2-(4-acylfuran-2-yl)acetamides in fair to good yields (54-81%) over 19 examples. The process takes place under relatively mild conditions and occurs via a mechanistic pathway involving C-H activation by oxidative monoamincarbonylation of the terminal triple bond of the substrates with formation of 2-ynamide intermediates, followed by 5---cyclization (via intramolecular conjugate addition of the in situ formed enolate to the 2-ynamide moiety) and aromative isomerization.

View Article and Find Full Text PDF

Recent progress in the oxidative coupling of unactivated Csp-H bonds with other C-H bonds.

Chem Commun (Camb)

December 2021

Department of Chemistry, Fudan University, 2005 Songhu Rd, Shanghai, 200438, China.

Article Synopsis
  • - The article discusses the oxidative coupling of carbon-hydrogen (C-H) bonds as a simple and efficient way to create carbon-carbon (C-C) bonds from hydrocarbons without needing any prior modifications.
  • - It highlights recent advancements in coupling unactivated Csp-H bonds with various hybrid C-H bonds, including combinations with Csp-H bonds.
  • - The paper provides a summary of the types of substrates used, proposed reaction mechanisms, and potential applications, aiming to inspire new methods for building Csp-C bonds effectively.
View Article and Find Full Text PDF

Metal-Catalyzed Decarboxylative C-H Functionalization.

Chem Rev

July 2017

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou, Fujian 350002, China.

Article Synopsis
  • C-H bond activation and decarboxylation are important techniques in organic synthesis, leading to a new method called decarboxylative C-H bond functionalization.! -
  • This review highlights recent advancements in utilizing this method to synthesize various organic compounds, including styrenes, chalcones, and heterocycles.! -
  • The article discusses the effectiveness, limitations, and potential applications of decarboxylative functionalization across different types of C-H bonds.!
View Article and Find Full Text PDF

Synthesis of bicyclic p-diiodobenzenes via silver-catalyzed Csp-H iodination and ruthenium-catalyzed cycloaddition.

J Am Chem Soc

June 2006

Department of Applied Chemistry Graduate School of Engineering, Nagoya University, Chikusa, Nagoya 464-8603, Japan.

Highly substituted iodobenzenes were efficiently and regioselectively synthesized from readily available 1,6-diynes via two-step process consisting of silver-catalyzed Csp-H iodination and subsequent ruthenium-catalyzed [2 + 2 + 2] cycloaddition of resultant iododiynes. Some of the obtained iodobenzenes were subjected to palladium-catalyzed C-C bond-forming reactions such as Mizoroki-Heck reaction, Sonogashira reaction, and Suzuki-Miyaura coupling, giving highly conjugated molecules.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!