High-efficiency catalytic reduction of residual oxygen for purification of carbon dioxide streams from high-pressure oxy-combustion systems

2021 ◽  
Author(s):  
Hong Lu ◽  
Luke Schideman ◽  
Qing Ye ◽  
Yongqi Lu
Keyword(s):  
Carbon Dioxide ◽  
High Efficiency ◽  
Catalytic Reduction ◽  
Reverse Flow ◽  
Fixed Bed ◽  
Flue Gases ◽  
Fixed Bed Reactor ◽  
Composite Catalysts ◽  
Residual Oxygen ◽  
Excellent Activity

Cobalt–manganese composite catalysts in a reverse-flow fixed-bed reactor showed excellent activity and selectivity for reduction of residual O2 for CO2 purification from pressurized oxy-combustion flue gases.

Efficient Recovery of Carbon Dioxide from Flue Gases of Coal-Fired Power Plants by Cyclic Fixed-Bed Operations over K2CO3-on-Carbon

1998 ◽  
Vol 37 (1) ◽  
pp. 185-191 ◽  
Author(s):  
Hiromu Hayashi ◽  
Jun Taniuchi ◽  
Nobuyoshi Furuyashiki ◽  
Shigeru Sugiyama ◽  
Shinichi Hirano ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Power Plants ◽  
Fixed Bed ◽  
Flue Gases ◽  
Efficient Recovery

Preparation and Performance of Several Non-Precious Metal Oxides Catalysts for the Low Temperature SCR of NOx with NH3

2011 ◽  
Vol 356-360 ◽  
pp. 1528-1534
Author(s):  
Wei Fang Dong
Keyword(s):  
Low Temperature ◽  
Metal Oxides ◽  
Flue Gas ◽  
Precious Metal ◽  
Catalytic Reduction ◽  
Fixed Bed ◽  
Catalytic Performance ◽  
Fixed Bed Reactor ◽  
Low Temperature Scr ◽  
Scr Of Nox

A series of non-precious metal oxides catalysts were prepared for low-temperature selective catalytic reduction (SCR) of NOx with NH3 in a fixed bed reactor. The catalytic performance was evaluated by the removal efficiency of NOx and N2selectivity which were respectively detected by flue gas analyzer and flue gas chromatograph. Furthermore, the components of gas products from the above experiments were analysed with 2010 GC-MS. The results illustrated that the MnO2exhibited the highest NOx conversion to 95.46% and the highest selectivity of N2to 100% at temperature of 393K, then followed ZrO2, Al2O3and Fe2O3.

Experimental Study of the Reforming of Methane with Carbon Dioxide over Coal Char

2008 ◽  
Vol 6 (1) ◽  
Author(s):  
Yanbing Li ◽  
Rui Xiao ◽  
Baosheng Jin ◽  
Huiyan Zhang
Keyword(s):  
Carbon Dioxide ◽  
Flow Rate ◽  
Fixed Bed ◽  
Coke Oven ◽  
Fixed Bed Reactor ◽  
Internal Diameter ◽  
Generation System ◽  
Coke Oven Gas ◽  
Surface Areas ◽  
Conversion Of Methane

As one of the fundamental issues of the new poly-generation system on the basis of gasification gas and coke oven gas, carbon dioxide reforming of methane experiments have been performed over coal chars derived from different parent coals in a lab-scale fixed-bed reactor (internal diameter 12 mm, length 700 mm). The char derived from TongChuan coal exhibited higher activity than other samples employed under the same conditions. After the reforming reaction, the char samples were covered with different amounts of carbon deposition which resulted in the surface areas decrease. As the flow rate of feed gas increased from 200 ml/min to 600 ml/min over the Xuzhou char sample at 1050 degrees Celsius, the conversion of methane decreased from 52.7% to 17.5% and the H2 /CO dropped from 0.75 to 0.55. While maintaining the flow rate of CO2 at 20ml/min at 1050 degrees Celsius, the mole ratio of reactants CH4/CO2 was varied from 1 to 1.75 which led to the H2/CO ratio increase from 0.75 to 1.2.

Denitrification Activities of Mo-V-Ti Catalysts Prepared by Dipping Method at Low Temperature

2018 ◽  
Vol 913 ◽  
pp. 900-906
Author(s):  
Dong Zhu Ma ◽  
Jian Li ◽  
Di Yin ◽  
Yuan Huang ◽  
Rui Min Wang ◽  
...  
Keyword(s):  
Low Temperature ◽  
Conversion Efficiency ◽  
Flue Gas ◽  
Catalytic Reduction ◽  
Fixed Bed ◽  
Space Velocity ◽  
Fixed Bed Reactor ◽  
Optimum Ratio ◽  
Denitrification Activity ◽  
Gas Space

Mo-V-Ti catalysts of low temperature denitrification were prepared by dipping method. In order to study the activity of selective catalytic reduction, the catalyst was placed in a fixed bed reactor. Industrial flue gas was simulated with cylinder gas. The experimental condition is NO: 500ppm, NH3:500ppm, O2:8%, SO2:100ppm, N2: equilibrium gas, space velocity: 36000h-1. Results indicate that the catalyst prepared by dipping method had good denitrification activity and sulfur resistance at low temperature. The optimum ratio of catalyst was 3V2O5-6MoO3-91TiO2 (wt %). The conversion efficiency of NO was 80~93%, and the conversion efficiency of SO2 was less than 1% at 180~260 °C.

Hydrate-Based Carbon Capture Process: Assessment of Various Packed Bed Systems for Boosted Kinetics of Hydrate Formation

2020 ◽  
Vol 143 (3) ◽  
Author(s):  
Amit Arora ◽  
Asheesh Kumar ◽  
Gaurav Bhattacharjee ◽  
Chandrajit Balomajumder ◽  
Pushpendra Kumar
Keyword(s):  
Carbon Dioxide ◽  
Carbon Capture ◽  
Carbon Dioxide Capture ◽  
Fixed Bed ◽  
Hydrate Formation ◽  
Packed Bed ◽  
Fixed Bed Reactor ◽  
Capture Process ◽  
Novel Technologies ◽  
Kinetics Of

Abstract The case for developing novel technologies for carbon dioxide (CO2) capture is fast gaining traction owing to increasing levels of anthropogenic CO2 being emitted into the atmosphere. Here, we have studied the hydrate-based carbon dioxide capture and separation process from a fundamental viewpoint by exploring the use of various packed bed media to enhance the kinetics of hydrate formation using pure CO2 as the hydrate former. We established the fixed bed reactor (FBR) configuration as a superior option over the commonly used stirred tank reactor (STR) setups typically used for hydrate formation studies by showing enhanced hydrate formation kinetics using the former. For the various packing material studied, we have observed silica gel with 100 nm pore size to return the best kinetic performance, corresponding to a water to hydrate conversion of 28 mol% for 3 h of hydrate growth. The fundamental results obtained in the present study set up a solid foundation for follow-up works with a more applied perspective and should be of interest to researchers working in the carbon dioxide capture and storage and gas hydrate fields alike.

Sign in / Sign up

Export Citation Format

Share Document