TY - JOUR
T1 - Hierarchically porous zirconium-based metal–organic frameworks for rapid adsorption and enrichment of sulfonamide antibiotics
AU - Han, Lizhen
AU - Qin, Peige
AU - Li, Mengyuan
AU - Li, Dan
AU - Mu, Mengyao
AU - Gao, Yanmei
AU - Zhu, Shiping
AU - Lu, Minghua
AU - Cai, Zongwei
N1 - This work was sponsored by National Natural Science Foundation of China (22076038), Natural Science Foundation of Henan Province , China (202300410044), and Henan key scientific research programs to Universities and Colleges (22ZX003).
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/1/15
Y1 - 2023/1/15
N2 - Due to serious risk to human health and eco-environmental security, antibiotics in water and foods received considerable concern. Herein, a series of stable hierarchically porous zirconium-based metal–organic frameworks (MOFs) namely HP-NU-902-X were prepared via modulator-induced defect-guided formation strategy for the first time and functioned as sorbents to removal and preconcentration of sulfonamide antibiotics (SAs). The pore size and specific surface area of HP-NU-902-X were systematically adjusted by changing concentration of monocarboxylic acid modulator. The adsorption performance of HP-NU-902-X were greatly improved by forming defects. Experiments demonstrated that HP-NU-902-80 possessed the highest adsorption efficiency to SAs. The limits of detection (S/N = 3) were achieved ranging 0.08 to 0.25 ng/mL. The spiked recoveries of water and milk samples were obtained in the range of 70.34–103.4 % and 73.83–100.5 %. Enrichment factors were calculated between 203 and 358. The SAs can be completely removed within 10 min, and adsorption kinetic data was best consistent with pseudo-second-order model. Using Langmuir isotherm model, maximum adsorption capacities for sulfadiazine, sulfapyridine, sulfametoxydiazine, sulfachloropyridazine, sulfabenzamide and sulfamethazine were calculated as 279.9, 467.7, 414.4, 433.1, 415.5 and 336.6 mg/g, respectively. The improved adsorption capacity was mainly owing to high surface area and extra defect sites. This synthetic strategy provides a way to prepare stable defective MOFs and enhance their potential applications in removal and extraction of environmental pollutants.
AB - Due to serious risk to human health and eco-environmental security, antibiotics in water and foods received considerable concern. Herein, a series of stable hierarchically porous zirconium-based metal–organic frameworks (MOFs) namely HP-NU-902-X were prepared via modulator-induced defect-guided formation strategy for the first time and functioned as sorbents to removal and preconcentration of sulfonamide antibiotics (SAs). The pore size and specific surface area of HP-NU-902-X were systematically adjusted by changing concentration of monocarboxylic acid modulator. The adsorption performance of HP-NU-902-X were greatly improved by forming defects. Experiments demonstrated that HP-NU-902-80 possessed the highest adsorption efficiency to SAs. The limits of detection (S/N = 3) were achieved ranging 0.08 to 0.25 ng/mL. The spiked recoveries of water and milk samples were obtained in the range of 70.34–103.4 % and 73.83–100.5 %. Enrichment factors were calculated between 203 and 358. The SAs can be completely removed within 10 min, and adsorption kinetic data was best consistent with pseudo-second-order model. Using Langmuir isotherm model, maximum adsorption capacities for sulfadiazine, sulfapyridine, sulfametoxydiazine, sulfachloropyridazine, sulfabenzamide and sulfamethazine were calculated as 279.9, 467.7, 414.4, 433.1, 415.5 and 336.6 mg/g, respectively. The improved adsorption capacity was mainly owing to high surface area and extra defect sites. This synthetic strategy provides a way to prepare stable defective MOFs and enhance their potential applications in removal and extraction of environmental pollutants.
KW - Adsorption
KW - Dispersive solid-phase extraction
KW - HP-NU-902
KW - Metal–organic frameworks
KW - Sample pretreatment
KW - Sulfonamide antibiotics
UR - http://www.scopus.com/inward/record.url?scp=85145610090&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2022.140969
DO - 10.1016/j.cej.2022.140969
M3 - Journal article
AN - SCOPUS:85145610090
SN - 1385-8947
VL - 456
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 140969
ER -