TY - JOUR
T1 - Achieving highly selective CO2 adsorption on SAPO-35 zeolites by template-modulating the framework silicon content
AU - Li, Yan
AU - Chen, Hongwei
AU - Wang, Chaoran
AU - Ye, Yu
AU - Li, Libo
AU - Song, Xiaowei
AU - Yu, Jihong
N1 - Publisher Copyright:
© 2022 The Royal Society of Chemistry.
PY - 2022/4/19
Y1 - 2022/4/19
N2 - Small-pore silicoaluminophosphate (SAPO) zeolites with 8-ring pore windows and appropriate acidities/polarities, for example, SAPO-34 (CHA) and SAPO-56 (AFX), have proven to be potential adsorbing materials for selective adsorption of CO2. However, SAPO-35 zeolites (LEV framework topology) synthesized using conventional templates are less reported for highly selective CO2 adsorption which might be due to inappropriate Si contents and acidities in the framework. In this work, by using N-methylpiperidine (NMP) as a template, SAPO-35 zeolites with various Si contents were synthesized under hydrothermal conditions, which allowed SAPO-35 zeolites with modulated acidities and polarities. The CO2 adsorption and separation properties of SAPO-35_x (x: Si/(Si + P + Al) in molar ratio) were investigated, and a close relationship between the acidity, polarity and CO2 adsorption and separation capacity was revealed. SAPO-35_0.14 with the strongest acidity showed the highest CO2 uptake of 4.76 mmol g−1 (273 K and 100 kPa), and appeared to be one of the best SAPO materials for CO2 adsorption. Moreover, increased Brønsted acidity can significantly enhance the adsorption selectivity of CO2 over N2. At 298 K and 100 kPa, SAPO-35_0.14 showed the highest CO2/N2 selectivity of 49.9, exhibiting potential for industrial processes. Transient binary breakthrough experiments on SAPO-35_0.14 further proved the efficient separation performance and stable circulation. The results of this study prove that the framework Si content of SAPO-35 zeolites is essential for regulating their CO2 adsorption performance. This work demonstrates that modulating the silicon content and acidity in SAPO zeolites via a suitable choice of template, as well as polarity, is of great significance for the rational synthesis of zeolites with superior CO2 adsorption and separation abilities.
AB - Small-pore silicoaluminophosphate (SAPO) zeolites with 8-ring pore windows and appropriate acidities/polarities, for example, SAPO-34 (CHA) and SAPO-56 (AFX), have proven to be potential adsorbing materials for selective adsorption of CO2. However, SAPO-35 zeolites (LEV framework topology) synthesized using conventional templates are less reported for highly selective CO2 adsorption which might be due to inappropriate Si contents and acidities in the framework. In this work, by using N-methylpiperidine (NMP) as a template, SAPO-35 zeolites with various Si contents were synthesized under hydrothermal conditions, which allowed SAPO-35 zeolites with modulated acidities and polarities. The CO2 adsorption and separation properties of SAPO-35_x (x: Si/(Si + P + Al) in molar ratio) were investigated, and a close relationship between the acidity, polarity and CO2 adsorption and separation capacity was revealed. SAPO-35_0.14 with the strongest acidity showed the highest CO2 uptake of 4.76 mmol g−1 (273 K and 100 kPa), and appeared to be one of the best SAPO materials for CO2 adsorption. Moreover, increased Brønsted acidity can significantly enhance the adsorption selectivity of CO2 over N2. At 298 K and 100 kPa, SAPO-35_0.14 showed the highest CO2/N2 selectivity of 49.9, exhibiting potential for industrial processes. Transient binary breakthrough experiments on SAPO-35_0.14 further proved the efficient separation performance and stable circulation. The results of this study prove that the framework Si content of SAPO-35 zeolites is essential for regulating their CO2 adsorption performance. This work demonstrates that modulating the silicon content and acidity in SAPO zeolites via a suitable choice of template, as well as polarity, is of great significance for the rational synthesis of zeolites with superior CO2 adsorption and separation abilities.
UR - http://www.scopus.com/inward/record.url?scp=85129930338&partnerID=8YFLogxK
U2 - 10.1039/d2sc00702a
DO - 10.1039/d2sc00702a
M3 - Article
AN - SCOPUS:85129930338
SN - 2041-6520
VL - 13
SP - 5687
EP - 5692
JO - Chemical Science
JF - Chemical Science
IS - 19
ER -