A highly active and efficient thin-felt Al-fiber-structured Co-MnO x composite oxide catalyst (named Co-MnO x -Al) with unique form factor and high permeability is developed for highthroughput catalytic decomposition of gaseous ozone (O 3 ). Thin-sheet Al-fiber felt (60 μm diameter; 90 vol % voidage) chips underwent a steam-only oxidation and calcination for endogenously growing a 0.7-μm-thick mesoporous layer of γ-Al 2 O 3 nanosheets along with the Al-fiber. Cobalt and manganese were placed onto the ns-γ-Al 2 O 3 /Al-fiber chips by incipient wetness co-impregnation method. The best catalyst is the one with a Co/Mn molar ratio of 0.36 and Co-Mn loading of 5 wt % after calcining at 500°C (named Co-MnO x (0.36)-Al), being able to achieve full O 3 conversion at 25°C for a feed gas containing 1000 � 30 ppm O 3 , using a high gas hourly space velocity of 48000 mL g cat.À 1 h À 1 ; full O 3 conversion is retained in the absence of moisture till the testing end after 720 min; in case with a relative humidity of 50 %, O 3 conversion slides from 88 % of the initial value to a flat of~66 % within 90 min. CoO x modification is paramount for improved formation of Mn 2 + species while leading to the highest fraction of (Mn 2 + + Mn 3 + ) in total (Mn 2 + + Mn 3 + + Mn 4 + ) and more oxygen vacancies on Co-MnO x (0.36)-Al catalyst surface.[a] L.
The Cover Feature shows a decoupling of CO2 utilization from the H2 economy. We review catalyst and reactor technologies for bulk chemical synthesis using CO2 and emerging feedstocks without any direct H2 input. These carbon recycling pathways are not contingent on the high cost of renewable H2. Approximately 1 Gt of CO2 can be potentially converted to bulk chemicals this way, avoiding the consumption of 29 Mt H2. More information can be found in the Review by L. Tao et al.
Decarbonizing the chemical industry will eventually entail using CO 2 as a feedstock for chemical synthesis. However, many chemical syntheses involve CO 2 reduction using inputs such as renewable hydrogen. In this review, chemical processes are discussed that use CO 2 as an oxidant for upgrading hydrocarbon feedstocks. The captured CO 2 is inherently reduced by the hydrocarbon co-reactants without consuming molecular hydrogen or renewable electricity. This CO 2 utilization approach can be potentially applied to synthesize eight emission-intensive molecules, including olefins and epoxides. Catalytic systems and reactor concepts are discussed that can overcome practical challenges, such as thermodynamic limitations, overoxidation, coking, and heat management. Under the best-case scenario, these hydrogen-free CO 2 reduction processes have a combined CO 2 abatement potential of approximately 1 gigatons per year and avoid the consumption of 1.24 PWh renewable electricity, based on current market demand and supply.
While metal−organic frameworks (MOFs) are promising gas adsorbents, their tortuous microporous structures cause additional resistance for gas diffusion, thus hindering the accessibility of interior active sites. Here, we present a practical strategy to incorporate missing cluster defects into a representative low-coordinated MOFs structure, Mg-MOF-74, while maintaining the stability of a defect-rich structure. In this proposed method, graphene oxide (GO) is employed as modulator, and crystallization time is varied to promote defect formation by altering the nucleation and crystal growth processes. The best performing GOmodified Mg-MOF-74 sample (MOF@GO 40 h) achieved 18% and 15% improvement in surface area and total pore volume, respectively, over pristine Mg-MOF-74. The reduced diffusion resistance to gas flow translates to increased accessibility for gas molecules to active Mg adsorption sites inside the MOFs, leading to enhanced CO 2 capture performance; the CO 2 uptake quantity of MOF@GO 40 h arrives at 6.06 mmol/g at 0.1 bar and at 9.17 mmol/g at 1 bar and 25 °C, 19.29% and 16.37% higher, respectively, than that of the pristine Mg-MOF-74, with a CO 2 /N 2 selectivity around 17.36% greater than that of pristine Mg-MOF-74. Our study demonstrates a facile approach for incorporating defects into MOFs systems with low coordination environments, thus expanding the library of defect-rich MOFs beyond the current highly coordinated MOF systems.
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