TY - JOUR
T1 - Use of covalent organic framework TpPa(OH)2 as pH-responsive adsorbent for copper ions from water
AU - Liao, Jun Bo
AU - Chang, Jo Shu
AU - Lee, Duu Jong
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/5/1
Y1 - 2023/5/1
N2 - For the first time, this study applied the covalent organic framework TpPa(OH)2 as a pH-responsive adsorbent for copper ions from water. The Langmuir adsorption capacities at pH 7 and 25, 35, and 45 °C are 56.2, 84.8, and 109.9 mg copper ions/g, respectively, an endothermic and entropy-driven process. The adsorption capacity of TpPa(OH)2 on copper ions at pH −0.2 and 35 °C is reduced to 11.3 mg/g, an 86.7% loss. The layered structures of TpPa(OH)2 are deteriorated by proton attacks at pH −0.2. The pH-swing (7, −0.2, then 7) increases the Langmuir capacity at pH 7 by 35.5%, contributed by excess sites of the exfoliated layers. The TpPa(OH)2 can be applied as a pH-responsive adsorbent, adsorbing 109.5 ± 3.2 mg copper ions/g at pH 7 and releasing 82.6% adsorbed copper ions at pH −0.2.
AB - For the first time, this study applied the covalent organic framework TpPa(OH)2 as a pH-responsive adsorbent for copper ions from water. The Langmuir adsorption capacities at pH 7 and 25, 35, and 45 °C are 56.2, 84.8, and 109.9 mg copper ions/g, respectively, an endothermic and entropy-driven process. The adsorption capacity of TpPa(OH)2 on copper ions at pH −0.2 and 35 °C is reduced to 11.3 mg/g, an 86.7% loss. The layered structures of TpPa(OH)2 are deteriorated by proton attacks at pH −0.2. The pH-swing (7, −0.2, then 7) increases the Langmuir capacity at pH 7 by 35.5%, contributed by excess sites of the exfoliated layers. The TpPa(OH)2 can be applied as a pH-responsive adsorbent, adsorbing 109.5 ± 3.2 mg copper ions/g at pH 7 and releasing 82.6% adsorbed copper ions at pH −0.2.
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U2 - 10.1016/j.matlet.2023.134061
DO - 10.1016/j.matlet.2023.134061
M3 - Article
AN - SCOPUS:85150443592
SN - 0167-577X
VL - 338
JO - Materials Letters
JF - Materials Letters
M1 - 134061
ER -