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The triple mechanisms of atenolol adsorption on ca-montmorillonite: Implication in pharmaceutical wastewater treatment

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The triple mechanisms of atenolol adsorption on ca-montmorillonite: Implication in pharmaceutical wastewater treatment. / Chang, Po Hsiang; Jiang, Wei Teh; Sarkar, Binoy et al.
In: Materials, Vol. 12, No. 18, 2858, 05.09.2019.

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Chang PH, Jiang WT, Sarkar B, Wang W, Li Z. The triple mechanisms of atenolol adsorption on ca-montmorillonite: Implication in pharmaceutical wastewater treatment. Materials. 2019 Sept 5;12(18):2858. doi: 10.3390/ma12182858

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@article{d08403a94e364ca683118ebfd4069508,
title = "The triple mechanisms of atenolol adsorption on ca-montmorillonite: Implication in pharmaceutical wastewater treatment",
abstract = "The adsorption of atenolol (AT) from aqueous solutions by Ca-montmorillonite (SAz-2) was investigated in batch studies under different physicochemical conditions. The AT existed in neutral un-dissociated form at pH 10, and was adsorbed on dioctahedral smectite (SAz-2) obeying the Langmuir isotherm with a maximum adsorption capacity of 330 mmol/kg. The kinetic adsorption suggested that both strong and weak adsorption sites existed on SAz-2 and participated in the adsorption mechanisms. The amount of exchangeable cations desorbed from SAz-2 during AT adsorption was linearly correlated with the amounts of adsorbed AT having slopes of 0.43, which implied that a cation exchange based adsorption mechanism was also in place. A comprehensive basal spacing change of SAz-2 was observed after AT adsorption on the clay mineral when tested with or without AT recrystallization. The intercalation of AT into the SAz-2 interlayers did not result in swelling due to the low adsorption capacity of the drug. Prominent interactions between the pharmaceutical molecule and SAz-2 were evidenced by apparent shifts of the infrared absorption bands after adsorption. The interlayer configurations and hydrogen bonding of AT on SAz-2 were also supported by infrared, X-ray diffraction and thermogravimetric analyses. This study suggested that SAz-2 is an excellent material to remove not only AT from pharmaceutical wastewater, but can potentially remove many other β-receptor blocker drugs. The results helped us to understand the possible interlayer configurations and adsorption mechanisms of the drugs on natural clay mineral based adsorbents.",
keywords = "Cation exchange, Clay minerals, Exfoliation, Hydrogen bonding, Pharmaceutical wastewater treatment, β-receptor blocker drugs",
author = "Chang, {Po Hsiang} and Jiang, {Wei Teh} and Binoy Sarkar and Wendong Wang and Zhaohui Li",
year = "2019",
month = sep,
day = "5",
doi = "10.3390/ma12182858",
language = "English",
volume = "12",
journal = "Materials",
issn = "1996-1944",
publisher = "MDPI AG",
number = "18",

}

RIS

TY - JOUR

T1 - The triple mechanisms of atenolol adsorption on ca-montmorillonite

T2 - Implication in pharmaceutical wastewater treatment

AU - Chang, Po Hsiang

AU - Jiang, Wei Teh

AU - Sarkar, Binoy

AU - Wang, Wendong

AU - Li, Zhaohui

PY - 2019/9/5

Y1 - 2019/9/5

N2 - The adsorption of atenolol (AT) from aqueous solutions by Ca-montmorillonite (SAz-2) was investigated in batch studies under different physicochemical conditions. The AT existed in neutral un-dissociated form at pH 10, and was adsorbed on dioctahedral smectite (SAz-2) obeying the Langmuir isotherm with a maximum adsorption capacity of 330 mmol/kg. The kinetic adsorption suggested that both strong and weak adsorption sites existed on SAz-2 and participated in the adsorption mechanisms. The amount of exchangeable cations desorbed from SAz-2 during AT adsorption was linearly correlated with the amounts of adsorbed AT having slopes of 0.43, which implied that a cation exchange based adsorption mechanism was also in place. A comprehensive basal spacing change of SAz-2 was observed after AT adsorption on the clay mineral when tested with or without AT recrystallization. The intercalation of AT into the SAz-2 interlayers did not result in swelling due to the low adsorption capacity of the drug. Prominent interactions between the pharmaceutical molecule and SAz-2 were evidenced by apparent shifts of the infrared absorption bands after adsorption. The interlayer configurations and hydrogen bonding of AT on SAz-2 were also supported by infrared, X-ray diffraction and thermogravimetric analyses. This study suggested that SAz-2 is an excellent material to remove not only AT from pharmaceutical wastewater, but can potentially remove many other β-receptor blocker drugs. The results helped us to understand the possible interlayer configurations and adsorption mechanisms of the drugs on natural clay mineral based adsorbents.

AB - The adsorption of atenolol (AT) from aqueous solutions by Ca-montmorillonite (SAz-2) was investigated in batch studies under different physicochemical conditions. The AT existed in neutral un-dissociated form at pH 10, and was adsorbed on dioctahedral smectite (SAz-2) obeying the Langmuir isotherm with a maximum adsorption capacity of 330 mmol/kg. The kinetic adsorption suggested that both strong and weak adsorption sites existed on SAz-2 and participated in the adsorption mechanisms. The amount of exchangeable cations desorbed from SAz-2 during AT adsorption was linearly correlated with the amounts of adsorbed AT having slopes of 0.43, which implied that a cation exchange based adsorption mechanism was also in place. A comprehensive basal spacing change of SAz-2 was observed after AT adsorption on the clay mineral when tested with or without AT recrystallization. The intercalation of AT into the SAz-2 interlayers did not result in swelling due to the low adsorption capacity of the drug. Prominent interactions between the pharmaceutical molecule and SAz-2 were evidenced by apparent shifts of the infrared absorption bands after adsorption. The interlayer configurations and hydrogen bonding of AT on SAz-2 were also supported by infrared, X-ray diffraction and thermogravimetric analyses. This study suggested that SAz-2 is an excellent material to remove not only AT from pharmaceutical wastewater, but can potentially remove many other β-receptor blocker drugs. The results helped us to understand the possible interlayer configurations and adsorption mechanisms of the drugs on natural clay mineral based adsorbents.

KW - Cation exchange

KW - Clay minerals

KW - Exfoliation

KW - Hydrogen bonding

KW - Pharmaceutical wastewater treatment

KW - β-receptor blocker drugs

U2 - 10.3390/ma12182858

DO - 10.3390/ma12182858

M3 - Journal article

AN - SCOPUS:85072561404

VL - 12

JO - Materials

JF - Materials

SN - 1996-1944

IS - 18

M1 - 2858

ER -