Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
MIL-101-NH2-TFR and MIL-101-NH2-TFR/Cu2+ as novel hybrid materials for efficient adsorption of iodine and reduction of Cr(VI). / Askari, Saeed; Khodaei, Mohammad Mehdi; Benassi, Enrico и др.
в: Materials Today Communications, Том 35, 105990, 06.2023.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
}
TY - JOUR
T1 - MIL-101-NH2-TFR and MIL-101-NH2-TFR/Cu2+ as novel hybrid materials for efficient adsorption of iodine and reduction of Cr(VI)
AU - Askari, Saeed
AU - Khodaei, Mohammad Mehdi
AU - Benassi, Enrico
AU - Jafarzadeh, Mohammad
N1 - This study was funded by Razi University with no grant number. Публикация для корректировки.
PY - 2023/6
Y1 - 2023/6
N2 - Today, due to the earnest jeopardies of environmental contaminants from various sources and their deteriorating effects on the ecosystem, the adsorption and reduction of these highly toxic pollutants with an efficient and cost-effective protocol can be considered a desirable phenomenon. Herein, a chromium-based metal-organic framework (MIL-101-NH2) was modified with thiourea and formaldehyde to form a polymeric layer on the surface (MIL-101-NH2-TFR). The resulting nanohybrid, as an adsorbent, was applied for efficient capture of iodine (I2) molecules from cyclohexane solution. MIL-101-NH2-TFR nanohybrid signified a superior adsorption performance for the capture of I2, compared to the pristine MIL-101-NH2, with a theoretical maximum uptake value of 625 mg/g and adsorption efficiency of 96.9 % through thionyl (C[dbnd]S), amino, and phenyl groups. The pseudo-second-order rate equation and the Langmuir model were best fitted for the I2 adsorption over MIL-101-NH2-TFR adsorbent. Quantum chemical calculations were conducted to reveal the mechanism of I2 adsorption onto the surface of MIL-101-NH2-TFR. Moreover, MIL-101-NH2-TFR was used to anchor Cu2+ to generate a catalytic system (MIL-101-NH2-TFR/Cu2+) for detoxification of Cr(VI) in the presence of formic acid as an eco-friendly reducing reagent in an aqueous medium. MIL-101-NH2-TFR and MIL-101-NH2-TFR/Cu2+ were reused several times for the adsorption/desorption process and the catalytic reduction, respectively.
AB - Today, due to the earnest jeopardies of environmental contaminants from various sources and their deteriorating effects on the ecosystem, the adsorption and reduction of these highly toxic pollutants with an efficient and cost-effective protocol can be considered a desirable phenomenon. Herein, a chromium-based metal-organic framework (MIL-101-NH2) was modified with thiourea and formaldehyde to form a polymeric layer on the surface (MIL-101-NH2-TFR). The resulting nanohybrid, as an adsorbent, was applied for efficient capture of iodine (I2) molecules from cyclohexane solution. MIL-101-NH2-TFR nanohybrid signified a superior adsorption performance for the capture of I2, compared to the pristine MIL-101-NH2, with a theoretical maximum uptake value of 625 mg/g and adsorption efficiency of 96.9 % through thionyl (C[dbnd]S), amino, and phenyl groups. The pseudo-second-order rate equation and the Langmuir model were best fitted for the I2 adsorption over MIL-101-NH2-TFR adsorbent. Quantum chemical calculations were conducted to reveal the mechanism of I2 adsorption onto the surface of MIL-101-NH2-TFR. Moreover, MIL-101-NH2-TFR was used to anchor Cu2+ to generate a catalytic system (MIL-101-NH2-TFR/Cu2+) for detoxification of Cr(VI) in the presence of formic acid as an eco-friendly reducing reagent in an aqueous medium. MIL-101-NH2-TFR and MIL-101-NH2-TFR/Cu2+ were reused several times for the adsorption/desorption process and the catalytic reduction, respectively.
KW - Cr(VI) reduction
KW - DFT
KW - Iodine adsorption
KW - MIL-101-NH2
KW - Metal-organic frameworks
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85153087794&origin=inward&txGid=451187f96e7895531d1575462211daf3
UR - https://www.mendeley.com/catalogue/7442d95b-fbe0-3dd1-a312-fe5517981535/
U2 - 10.1016/j.mtcomm.2023.105990
DO - 10.1016/j.mtcomm.2023.105990
M3 - Article
VL - 35
JO - Materials Today Communications
JF - Materials Today Communications
SN - 2352-4928
M1 - 105990
ER -
ID: 59290097