Selective adsorption of methylparaben by submicrosized molecularly imprinted polymer / Minjia Meng in Industrial & engineering chemistry research, Vol. 51 N° 45 (Novembre 2012)  

Public ISBD [article]  inIndustrial & engineering chemistry research > Vol. 51 N° 45 (Novembre 2012) . - pp. 14915–14924 Titre : Selective adsorption of methylparaben by submicrosized molecularly imprinted polymer : Batch and dynamic flow mode studies Type de document : texte imprimé Auteurs : Minjia Meng, Auteur ; Zhipeng Wang, Auteur ; Linli Ma, Auteur Année de publication : 2013 Article en page(s) : pp. 14915–14924 Note générale : Industrial chemistry Langues : Anglais (eng) Mots-clés : Adsorption Polymer Résumé : Highly selective submicrosized molecularly imprinted polymer (SMIPMP) for methylparaben (MP) was synthesized by molecular imprinting technique with a sol–gel process on silica submicroparticles. The prepared SMIPMP was characterized by FT-IR, SEM, TG, and N2 adsorption–desorption techniques. Compared with microsized methylparaben imprinted polymer (MMIPMP) adsorbent, SMIPMP adsorbent with small particle size and high specific surface area showed faster adsorption rate and stronger adsorption capacity for MP. The maximum static adsorption capacity for MP of SMIPMP was 32.68 mg g–1, and the adsorption equilibrium could be reached in 40 min. The SMIPMP adsorbent could be used at least 5 times without significant loss in adsorption capacity. Compared with submicrosized nonimprinted polymer (SNIP), SMIPMP indicated excellent recognition and binding affinity toward MP molecules, whose selectivity coefficients for MP relative to methyl salicylate (MS) and p-hydroxybenzoic acid (p-HB) were 5.664 and 6.129, respectively. The mechanism for static adsorption of MP onto SMIPMP was found to follow Freundlich, Redlich-Peterson isotherm, and pseudo-second-order model. Thomas’ model was applied in the quantitative description and parametrization of the dynamic adsorption of MP to SMIPMP and SNIP, which showed that the linear and nonlinear methods were both suitable to predict the breakthrough curves but the nonlinear method was better. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie301890b [article] Selective adsorption of methylparaben by submicrosized molecularly imprinted polymer : Batch and dynamic flow mode studies [texte imprimé] / Minjia Meng, Auteur ; Zhipeng Wang, Auteur ; Linli Ma, Auteur . - 2013 . - pp. 14915–14924. Industrial chemistry Langues : Anglais (eng) in Industrial & engineering chemistry research > Vol. 51 N° 45 (Novembre 2012) . - pp. 14915–14924 Mots-clés : Adsorption Polymer Résumé : Highly selective submicrosized molecularly imprinted polymer (SMIPMP) for methylparaben (MP) was synthesized by molecular imprinting technique with a sol–gel process on silica submicroparticles. The prepared SMIPMP was characterized by FT-IR, SEM, TG, and N2 adsorption–desorption techniques. Compared with microsized methylparaben imprinted polymer (MMIPMP) adsorbent, SMIPMP adsorbent with small particle size and high specific surface area showed faster adsorption rate and stronger adsorption capacity for MP. The maximum static adsorption capacity for MP of SMIPMP was 32.68 mg g–1, and the adsorption equilibrium could be reached in 40 min. The SMIPMP adsorbent could be used at least 5 times without significant loss in adsorption capacity. Compared with submicrosized nonimprinted polymer (SNIP), SMIPMP indicated excellent recognition and binding affinity toward MP molecules, whose selectivity coefficients for MP relative to methyl salicylate (MS) and p-hydroxybenzoic acid (p-HB) were 5.664 and 6.129, respectively. The mechanism for static adsorption of MP onto SMIPMP was found to follow Freundlich, Redlich-Peterson isotherm, and pseudo-second-order model. Thomas’ model was applied in the quantitative description and parametrization of the dynamic adsorption of MP to SMIPMP and SNIP, which showed that the linear and nonlinear methods were both suitable to predict the breakthrough curves but the nonlinear method was better. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie301890b

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