2016
DOI: 10.1080/19443994.2015.1012333
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Synthesis and evaluation of methacrylic acid functionalized β-cyclodextrin based molecular imprinted polymer for 2,4-dichlorophenol in water samples

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Cited by 12 publications
(5 citation statements)
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References 63 publications
(79 reference statements)
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“…3A. Strong absorption bands at around 3432, 2930 and 1700 cm −1 were observed, which could be attributed to the stretching vibration of C O, C H and O H in MAA [22]. Absorption bands at around 1600 and 1450 cm −1 were observed due to C C stretching vibration in benzene ring of DVB or MAA [23].…”
Section: Preparation and Characterization Of Mt-mipsmentioning
confidence: 90%
“…3A. Strong absorption bands at around 3432, 2930 and 1700 cm −1 were observed, which could be attributed to the stretching vibration of C O, C H and O H in MAA [22]. Absorption bands at around 1600 and 1450 cm −1 were observed due to C C stretching vibration in benzene ring of DVB or MAA [23].…”
Section: Preparation and Characterization Of Mt-mipsmentioning
confidence: 90%
“…[ 30 ] The binding ability of the MIP was superior to NIP owning to the supramolecularly imprinted hydrogen bonding interactions. Surikumaran and coworkers [ 31 ] linked MAA and β‐CD via toluene‐2,4‐diisocyanate (TDI) to prepare MAA‐TDI‐β‐CD as the functional monomer. The MAA‐TDI‐β‐CD MIP had a stronger binding ability to 2,4‐dichlorophenol (2,4‐DCP) in water samples than that of MAA‐MIP due to the triple interaction between MAA‐TDI‐β‐CD and 2,4‐DCP (hydrogen bonding, π–π interaction, and host–guest inclusion), whereas there were only hydrogen bonds between MAA and 2,4‐DCP without specificity.…”
Section: Molecularly Imprinted Polymers With Cyclodextrin As Functional Monomersmentioning
confidence: 99%
“…This is maybe because the phenols were retained on the NIP MAA-βCD by physical adsorption, and thus they were easily eluted in the washing step (15). The binding force between MIP MAA-βCD and the phenols in this study was mainly due to the inclusion complex formation between β-CD cavity and phenols and π-π interaction (between double bond of MAA in polymer network and π-electron from benzene ring of phenol compounds) besides the presence of imprinted cavities (38,40). This explains well the highest recoveries obtained for phenol compounds when MIP MAA-βCD was employed as the SPE material in this study.…”
Section: Comparison With Other Spe Sorbentsmentioning
confidence: 99%
“…The synthesis of MAA-βCD monomer was performed first according to some literature with slight modification (32,39) and then followed by synthesis of imprinted polymers which was reported in our previous works (38,40). First, the template molecule, 2,4-DCP (0.14 mmol) was dissolved in 60 mL DMAC in a flask.…”
Section: Synthesis Of Mip Maa-βcd Sorbentmentioning
confidence: 99%
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