SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Ström Henrik 1981)
 

Sökning: WFRF:(Ström Henrik 1981) > (2020-2024) > Complete Reaction C...

Complete Reaction Cycle for Methane-to-Methanol Conversion over Cu-SSZ-13: First-Principles Calculations and Microkinetic Modeling

Engedahl, Unni, 1990 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Boje, Astrid, 1991 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Ström, Henrik, 1981 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
visa fler...
Grönbeck, Henrik, 1966 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Hellman, Anders, 1974 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
visa färre...
 (creator_code:org_t)
2021-07-05
2021
Engelska.
Ingår i: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 125:27, s. 14681-14688
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The steadily increasing consumption of natural gas imposes a need to facilitate the handling and distribution of the fuel, which presently is compressed or condensed. Alternatively, reduced volatility and increased tractability are achieved by converting the chemical energy of the main component, methane, into liquid methanol. Previous studies have explored direct methane-to-methanol conversion, but suitable catalysts have not yet been identified. Here, the complete reaction cycle for methane-to-methanol conversion over the Cu-SSZ-13 system is studied using density functional theory. The first step in the reaction cycle is the migration of Cu species along the zeolite framework forming the Cu pair, which is necessary for the adsorption of O2. Methane conversion occurs over the CuOOCu and CuOCu sites, consecutively, after which the system is returned to its initial structure with two separate Cu ions. A density functional theory-based kinetic model shows high activity when water is included in the reaction mechanism, for example, even at very low partial pressures of water, the kinetic model results in a turnover frequency of ∼1 at 450 K. The apparent activation energy from the kinetic model (∼1.1 eV) is close to recent measurements. However, experimental studies always observe very small amounts of methanol compared to formation of more energetically preferred products, for example, CO2. This low selectivity to methanol is not described by the current reaction mechanism as it does not consider formation of other species; however, the results suggest that selectivity, rather than inherent kinetic limitations, is an important target for improving methanol yields from humid systems. Moreover, a closed reaction cycle for the partial oxidation of methane has long been sought, and in achieving this over the Cu-SSZ-13, this study contributes one more step toward identifying a suitable catalyst for direct methane-to-methanol conversion.

Ämnesord

NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Kemiteknik -- Annan kemiteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Chemical Engineering -- Other Chemical Engineering (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy