CeO2-modified CaO/Ca12Al14O33 bi-functional material for CO2 capture and H2 production in sorption-enhanced steam gasification of biomass

Energy ◽  
2020 ◽  
Vol 192 ◽  
pp. 116664 ◽  
Author(s):  
Xianyao Yan ◽  
Yingjie Li ◽  
Xiaotong Ma ◽  
Zhiguo Bian ◽  
Jianli Zhao ◽  
...  
2021 ◽  
Vol 11 (10) ◽  
pp. 4713
Author(s):  
Carlos Arnaiz del Pozo ◽  
Schalk Cloete ◽  
Ángel Jiménez Álvaro ◽  
Felix Donat ◽  
Shahriar Amini

The hydrogen economy has received resurging interest in recent years, as more countries commit to net-zero CO2 emissions around the mid-century. “Blue” hydrogen from natural gas with CO2 capture and storage (CCS) is one promising sustainable hydrogen supply option. Although conventional CO2 capture imposes a large energy penalty, advanced process concepts using the chemical looping principle can produce blue hydrogen at efficiencies even exceeding the conventional steam methane reforming (SMR) process without CCS. One such configuration is gas switching reforming (GSR), which uses a Ni-based oxygen carrier material to catalyze the SMR reaction and efficiently supply the required process heat by combusting an off-gas fuel with integrated CO2 capture. The present study investigates the potential of advanced La-Fe-based oxygen carrier materials to further increase this advantage using a gas switching partial oxidation (GSPOX) process. These materials can overcome the equilibrium limitations facing conventional catalytic SMR and achieve direct hydrogen production using a water-splitting reaction. Results showed that the GSPOX process can achieve mild efficiency improvements relative to GSR in the range of 0.6–4.1%-points, with the upper bound only achievable by large power and H2 co-production plants employing a highly efficient power cycle. These performance gains and the avoidance of toxicity challenges posed by Ni-based oxygen carriers create a solid case for the further development of these advanced materials. If successful, results from this work indicate that GSPOX blue hydrogen plants can outperform an SMR benchmark with conventional CO2 capture by more than 10%-points, both in terms of efficiency and CO2 avoidance.


Processes ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 462
Author(s):  
Houssame Boujjat ◽  
Sylvain Rodat ◽  
Stéphane Abanades

Solar biomass gasification is an attractive pathway to promote biomass valorization while chemically storing intermittent solar energy into solar fuels. The economic feasibility of a solar gasification process at a large scale for centralized H2 production was assessed, based on the discounted cash-flow rate of return method to calculate the minimum H2 production cost. H2 production costs from solar-only, hybrid and conventional autothermal biomass gasification were evaluated under various economic scenarios. Considering a biomass reference cost of 0.1 €/kg, and a land cost of 12.9 €/m2, H2 minimum price was estimated at 2.99 €/kgH2 and 2.48 €/kgH2 for the allothermal and hybrid processes, respectively, against 2.25 €/kgH2 in the conventional process. A sensitivity study showed that a 50% reduction in the heliostats and solar tower costs, combined with a lower land cost of below 0.5 €/m2, allowed reaching an area of competitiveness where the three processes meet. Furthermore, an increase in the biomass feedstock cost by a factor of 2 to 3 significantly undermined the profitability of the autothermal process, in favor of solar hybrid and solar-only gasification. A comparative study involving other solar and non-solar processes led to conclude on the profitability of fossil-based processes. However, reduced CO2 emissions from the solar process and the application of carbon credits are definitely in favor of solar gasification economics, which could become more competitive. The massive deployment of concentrated solar energy across the world in the coming years can significantly reduce the cost of the solar materials and components (heliostats), and thus further alleviate the financial cost of solar gasification.


2013 ◽  
Author(s):  
Saeed Danaei Kenarsari ◽  
Yuan Zheng

A lab-scale CO2 capture system is designed, fabricated, and tested for performing CO2 capture via carbonation of very fine calcium oxide (CaO) with particle size in micrometers. This system includes a fixed-bed reactor made of stainless steel (12.7 mm in diameter and 76.2 mm long) packed with calcium oxide particles dispersed in sand particles; heated and maintained at a certain temperature (500–550°C) during each experiment. The pressure along the reactor can be kept constant using a back pressure regulator. The conditions of the tests are relevant to separation of CO2 from combustion/gasification flue gases and in-situ CO2 capture process. The inlet flow, 1% CO2 and 99% N2, goes through the reactor at the flow rate of 150 mL/min (at standard conditions). The CO2 percentage of the outlet gas is monitored and recorded by a portable CO2 analyzer. Using the outlet composition, the conversion of calcium oxide is figured and employed to develop the kinetics model. The results indicate that the rates of carbonation reactions considerably increase with raising the temperature from 500°C to 550°C. The conversion rates of CaO-carbonation are well fitted to a shrinking core model which combines chemical reaction controlled and diffusion controlled models.


2018 ◽  
Vol 230 ◽  
pp. 1660-1672 ◽  
Author(s):  
Tien-Lin Hsieh ◽  
Dikai Xu ◽  
Yitao Zhang ◽  
Sourabh Nadgouda ◽  
Dawei Wang ◽  
...  

Energy ◽  
2015 ◽  
Vol 88 ◽  
pp. 9-17 ◽  
Author(s):  
Kristin Jordal ◽  
Rahul Anantharaman ◽  
Thijs A. Peters ◽  
David Berstad ◽  
John Morud ◽  
...  

Author(s):  
Peng Pei ◽  
Manohar Kulkarni

Integrated Gasification Combined Cycle (IGCC) is believed to be one of the most promising technologies to offer electricity and other de-carbon fuels with carbon capture requirement as well as to meet other emission regulations at a relatively low cost. As one of the most important parts, different gasification technologies can greatly influence the performance of the system. This paper develops a model to examine the feasibilities and advantages of using Ultra Superheated Steam (USS) gasification technology in IGCC power plant with carbon dioxide capture and storage (CCS). USS gasification technology converts coal into syngas by the endothermic steam reforming reaction, and the heat required for this reaction is provided by the sensible heat in the ultra superheated steam. A burner utilizes synthetic air (21% O2 and 79% H2O) to burn fuel gas to produce the USS flame for the gasification process. The syngas generated from USS gasification has a higher hydrogen fraction (more than 50%) then other gasification processes. This high ratio of hydrogen is considered to be desired for a “capture-ready” IGCC plant. After gas cleanup and water gas shift reaction, the syngas goes to the Selexol process for carbon dioxide removal. Detailed calculations and analysis are performed to test the performance of USS gasification technology used in IGCC generation systems. Final results such as net output, efficiency penalty for CO2 capture part, and net thermal efficiency are calculated and compared when three different coal types are used. This paper uses published data of USS gasification from previous research at the University of North Dakota. The model also tries to treat the IGCC with carbon dioxide capture system as a whole thermal system, the superheated steam used in USS gasification can be provided by extracting steam from the lower pressure turbine in the Rankine Cycle. The model will make reasonable use of various waste energies and steams for both mechanical and chemical processes to improve the performance of the plant, and incorporate CO2 capture system into the design concept of the power plant.


2018 ◽  
Vol 12 (5) ◽  
pp. 735-748 ◽  
Author(s):  
Zakir Khan ◽  
Suzana Yusup ◽  
Murni M Ahmad ◽  
Abrar Inayat ◽  
Muhammad Naqvi ◽  
...  

2019 ◽  
Vol 479 ◽  
pp. 25-30 ◽  
Author(s):  
Laura Proaño ◽  
Edisson Tello ◽  
Martha A. Arellano-Trevino ◽  
Shuoxun Wang ◽  
Robert J. Farrauto ◽  
...  

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