Hybrid catalytic materials with CO2 capture and oxygen transfer functionalities for high–purity H2 production

2020 ◽  
Author(s):  
Andy N. Antzaras ◽  
Eleni Heracleous ◽  
Angeliki A. Lemonidou
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 ◽  
...  

2018 ◽  
Vol 6 (9) ◽  
pp. 1777-1787 ◽  
Author(s):  
Lili Tan ◽  
Changlei Qin ◽  
Zhonghui Zhang ◽  
Jingyu Ran ◽  
Vasilije Manovic

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.


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.


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