Direct Conversion of Methane to Value-Added Chemicals over Heterogeneous Catalysts: Challenges and Prospects

2017 ◽  
Vol 117 (13) ◽  
pp. 8497-8520 ◽  
Author(s):  
Pierre Schwach ◽  
Xiulian Pan ◽  
Xinhe Bao
2018 ◽  
Vol 34 (5) ◽  
pp. 595-655 ◽  
Author(s):  
Mohammad Ghashghaee

Abstract The reduced availability of propylene and C4 products from steam crackers continues to provoke on-purpose technologies for light olefins such that almost 30% of propylene in 2025 is predicted to be supplied from unconventional sources. Furthermore, the recent discoveries of natural gas reservoirs have urged interest in the conversion of surplus alkanes and alkenes, especially ethane and ethylene. The direct conversion of ethylene to propylene or a combination of value-added chemicals, including butylenes and oligomers in the range of gasoline and diesel fuel, provides the capability of responding to the fluctuations in the balance between supply and demand of the main petrochemicals. A comprehensive review of heterogeneous catalysts for the gas-phase conversion pathways is presented here in terms of catalytic performances (ethylene conversion and product selectivities), productivities, lifetimes, active sites, physicochemical properties, mechanisms, influence of operating conditions, deactivation and some unresolved/less-advanced aspects of the field. The addressed catalysts cover both zeolitic materials and transition metals, such as tungsten, molybdenum, rhenium and nickel. Efforts in both experimental and theoretical studies are taken into account. Aside from the potential fields of progress, the review reveals very promising performances for the emerging technologies to produce propylene, a mixture of propylene and butenes, or a liquid fuel from ethylene.


2018 ◽  
Vol 2018 ◽  
pp. 1-21 ◽  
Author(s):  
Guangbi Li ◽  
Wei Liu ◽  
Chenliang Ye ◽  
Xiaoyun Li ◽  
Chuan-Ling Si

Chemocatalytic transformation of lignocellulosic biomass to value-added chemicals has attracted global interest in order to build up sustainable societies. Cellulose, the first most abundant constituent of lignocellulosic biomass, has received extensive attention for its comprehensive utilization of resource, such as its catalytic conversion into high value-added chemicals and fuels (e.g., HMF, DMF, and isosorbide). However, the low reactivity of cellulose has prevented its use in chemical industry due to stable chemical structure and poor solubility in common solvents over the cellulose. Recently, homogeneous or heterogeneous catalysis for the conversion of cellulose has been expected to overcome this issue, because various types of pretreatment and homogeneous or heterogeneous catalysts can be designed and applied in a wide range of reaction conditions. In this review, we show the present situation and perspective of homogeneous or heterogeneous catalysis for the direct conversion of cellulose into useful platform chemicals.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Jinshu Tian ◽  
Jiangqiao Tan ◽  
Zhaoxia Zhang ◽  
Peijie Han ◽  
Min Yin ◽  
...  

Abstract Direct oxidation of methane to value-added C1 chemicals (e.g. HCHO and CO) provides a promising way to utilize natural gas sources under relatively mild conditions. Such conversions remain, however, a key selectivity challenge, resulting from the facile formation of undesired fully-oxidized CO2. Here we show that B2O3-based catalysts are selective in the direct conversion of methane to HCHO and CO (~94% selectivity with a HCHO/CO ratio of ~1 at 6% conversion) and highly stable (over 100 hour time-on-stream operation) conducted in a fixed-bed reactor (550 °C, 100 kPa, space velocity 4650 mL gcat−1 h−1). Combined catalyst characterization, kinetic studies, and isotopic labeling experiments unveil that molecular O2 bonded to tri-coordinated BO3 centers on B2O3 surfaces acts as a judicious oxidant for methane activation with mitigated CO2 formation, even at high O2/CH4 ratios of the feed. These findings shed light on the great potential of designing innovative catalytic processes for the direct conversion of alkanes to fuels/chemicals.


2017 ◽  
Vol 19 (8) ◽  
pp. 1969-1982 ◽  
Author(s):  
Deepak Verma ◽  
Rizki Insyani ◽  
Young-Woong Suh ◽  
Seung Min Kim ◽  
Seok Ki Kim ◽  
...  

For realizing sustainable bio-based refineries, it is crucial to obtain high yields of value-added chemicalsviadirect conversion of cellulose and lignocellulosic biomass.


Zeolites ◽  
1992 ◽  
Vol 12 (8) ◽  
pp. 882-888 ◽  
Author(s):  
M.A. Bañares ◽  
B. Pawelec ◽  
J.L.G. Fierro

RSC Advances ◽  
2021 ◽  
Vol 11 (49) ◽  
pp. 31058-31061
Author(s):  
Amy J. Knorpp ◽  
Ana B. Pinar ◽  
Mark A. Newton ◽  
Teng Li ◽  
Adelaide Calbry-Muzyka ◽  
...  

The synthesis and selection of large-port mordenite is critical for optimizing productivity for the direct conversion of methane to methanol.


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