Fe3O4 nanoparticles coated with a guanidinium-functionalized polyelectrolyte extend the pH range for phosphate binding. Issue 35 (11th August 2017)

• Record Type: Journal Article
• Authors: Paltrinieri, Laura; Wang, Min; Sachdeva, Sumit; Besseling, Nicolaas A. M.; Sudhölter, Ernst J. R.; de Smet, Louis C. P. M.
• Is Part Of: Journal of materials chemistry. Volume 5:Issue 35(2017)
• Page Start: 18476
• Page End: 18485
• Publication Date: 2017-08-11
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c7ta04054g
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : This work shows the enhanced effect of functional coatings on phosphate adsorption at alkaline conditions using Fe3 O4 NPs. Abstract : In this work commercially available Fe3 O4 NPs were coated with polyallylamine hydrochloride (PAH) and PAH functionalized with guanidinium groups (PAH–Gu) for investigating the phosphate adsorption properties under alkaline conditions. The coating can be prepared easily and rapidly and results in Fe3 O4 NPs with improved properties related to phosphate binding and colloidal stability. At a low initial phosphate concentration (2 mg L −1 ), the novel Fe3 O4 @PAH–Gu material was able to remove phosphate rather independently of the pH condition (4.0, 3.6 and 3.7 mg g −1 at pH = 5, 8 and 10, respectively), whereas for the uncoated Fe3 O4 NPs the amount of adsorbed phosphate drops by >75% upon changing from acidic to alkaline conditions (0.84 mg g −1 at pH = 10). Under alkaline conditions, the fastest adsorption was observed for Fe3 O4 @PAH–Gu followed by Fe3 O4 @PAH and Fe3 O4 . This can be related to the additional interaction forces due to the presence of primary amine groups (in PAH and PAH–Gu) and Gu groups (in PAH–Gu only) in coatings. Over 80% of the phosphate adsorbed on the novel Fe3 O4 @PAH–Gu material was successfully desorbed and the coated NPs were re-used over three adsorption/desorption cycles. This work will stimulate the design and preparation of functionalized polyelectrolytes for an extended area of applications, especially for the selective removal of target compounds from wastewater.