scholarly journals Multicycle Performance of CaTiO3 Decorated CaO-Based CO2 Adsorbent Prepared by a Versatile Aerosol Assisted Self-Assembly Method

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3188
Author(s):  
Ren-Wei Chang ◽  
Chin-Jung Lin ◽  
Ya-Hsuan Liou

Calcium oxide (CaO) is a promising adsorbent to separate CO2 from flue gas. However, with cycling of carbonation/decarbonation at high temperature, the serious sintering problem causes its capture capacity to decrease dramatically. A CaTiO3-decorated CaO-based CO2 adsorbent was prepared by a continuous and simple aerosol-assisted self-assembly process in this work. Results indicated that CaTiO3 and CaO formed in the adsorbent, whereas CaO gradually showed a good crystalline structure with increased calcium loading. Owing to the high thermal stability of CaTiO3, it played a role in suppressing the sintering effect and maintaining repeated high-temperature carbonation and decarbonation processes. When the calcium and titanium ratio was 3, the CO2 capture capacity was as large as 7 mmol/g with fast kinetics. After 20 cycles under mild regeneration conditions (700 °C, N2), the performance of CO2 capture of CaTiO3-decorated CaO-based adsorbent nearly unchanged. Even after 10 cycles under severe regeneration conditions (920 °C, CO2), the performance of CO2 capture still remained nearly 70% compared to the first cycle. The addition of CaTiO3 induced good and firm CaO dispersion on its surface. Excellent kinetics and stability were evident.

Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2220 ◽  
Author(s):  
Szu-Chen Wu ◽  
Po-Hsueh Chang ◽  
Chieh-Yen Lin ◽  
Cheng-Hsiung Peng

In this study, Ca-based multi-metals metal-organic framework (CaMgAl-MOF) has been designed as precursor material for carbon dioxide (CO2) capture to enhance the CO2 capture capacity and stability during multiple carbonation-calcination cycles. The CaMgAl-MOFs were constructed from self-assembly of metal ions and organic ligands through hydrothermal process to make metal ions uniformly distributed through the whole structure. Upon heat treatment at 600 °C, the Ca-based multi-metals CaMgAl-MOF would gradually transform to CaO and MgO nanoparticles along with the amorphous aluminum oxide distributed in the CaO matrix. XRD, Fourier transform infrared (FTIR), and SEM were used to identify the structure and characterize the morphology. The CO2 capture capacity and multiple carbonation-calcination cyclic tests of calcined Ca-based metal-organic framework (MOF) (attached with O and indicated as Ca-MOF-O) were performed by thermal gravimetric analysis (TGA). The single metal component calcined Ca-MOF sorbent have the highest CO2 capture capacity up to 72 wt.%, but a lower stability of 61% due to severe particle aggregation. In contrast, a higher Ca-rich MOF oxide sorbent with tailoring the Mg/Al ratios, Ca0.97Mg0.025Al0.005-MOF-O, showed the best performance, not only having the high stability of ~97%, but also maintaining the highest capacity of 71 wt.%. The concept of using Ca-based MOF materials combined with mixed-metal ions for CO2 capture showed a potential route for achieving efficient multiple carbonation-calcination CO2 cycles.


ChemSusChem ◽  
2011 ◽  
Vol 4 (12) ◽  
pp. 1844-1851 ◽  
Author(s):  
Po-Hsueh Chang ◽  
Yen-Po Chang ◽  
San-Yuan Chen ◽  
Ching-Tsung Yu ◽  
Yau-Pin Chyou

2017 ◽  
Vol 22 (3) ◽  
pp. 215 ◽  
Author(s):  
Oscar H Ojeda-Niño ◽  
Carolina Blanco ◽  
Carlos E Daza

Hydroxyapatite (HAp) was obtained from tilapia scales by two extraction<br />methods: direct calcination and acid-base treatment. The physicochemical<br />characteristics of the obtained HAps were evaluated by thermogravimetric<br />analysis, X-ray fluorescence, X-ray diffraction, scanning electron microscopy, surface area, infrared spectroscopy, and basicity measurement at 298 K by CO2-pulse titration. Furthermore, the CO2 capture capacity of the solids at high temperature was also determined. Both methods showed the presence of a HAp phase although significant differences in the properties of the solids were found. The HAp obtained by direct calcination, exhibited a lower crystallinity and a greater surface area and basicity than the HAp obtained by the acid-base treatment. These features were correlated with the solid’s CO2 capture capacity. In this work, CO2 capture capacity values for HAp yielded by calcination ranged from 2.5 to 3.2 mg CO2 /g captured at 973 K, and for the acid-base treatment-derived HAp, CO2 capture capacity values between 1.2 to 2.5 mg CO2 /g were recorded. These results reveal the potential of HAps extracted from tilapia scales as solids with high CO2 capture capacity, thermal stability, and capture/release cycles reversibility.


2021 ◽  
Author(s):  
Manohara Gudiyor Veerabhadrappa ◽  
David Norris ◽  
Mercedes Maroto-Valer ◽  
Susana García

Layered double hydroxides (LDHs) based mixed metal oxides (MMOs) are promising high temperature CO2 capture sorbents. In order to improve their CO2 capture capacity, it is crucial to bring in...


2021 ◽  
Vol 12 (13) ◽  
pp. 4825-4835 ◽  
Author(s):  
Rajesh Belgamwar ◽  
Ayan Maity ◽  
Tisita Das ◽  
Sudip Chakraborty ◽  
Chathakudath P. Vinod ◽  
...  

Capturing CO2 before its release. Lithium silicate nanosheets showed high CO2 capture capacity (35.3 wt%) with ultra-fast kinetics (0.22 g g−1 min−1) and enhanced stability at 650 °C for at least 200 cycles, due to mixed-phase-model of CO2 capture.


2012 ◽  
Vol 55 ◽  
pp. 18-26 ◽  
Author(s):  
Qiang Wang ◽  
Hui Huang Tay ◽  
Zhanhu Guo ◽  
Luwei Chen ◽  
Yan Liu ◽  
...  

2016 ◽  
Vol 4 (3) ◽  
pp. 1439-1445 ◽  
Author(s):  
Jie Chen ◽  
Jie Yang ◽  
Gengshen Hu ◽  
Xin Hu ◽  
Zhiming Li ◽  
...  

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