2017
DOI: 10.1016/j.cej.2017.03.073
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Removal of perfluorooctanoic acid from water with economical mesoporous melamine-formaldehyde resin microsphere

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Cited by 72 publications
(23 citation statements)
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“…In addition, the strongest absorption at 1050 cm −1 was observed in the SF adhesive, corresponding to C–O bending [34]. The peak at 993 cm −1 was attributed to the –OH out-of-plane bending vibration [35,36]. A strong and sharp peak was found at 812 cm −1 , which was a characteristic of the triazine ring [37].…”
Section: Resultsmentioning
confidence: 99%
“…In addition, the strongest absorption at 1050 cm −1 was observed in the SF adhesive, corresponding to C–O bending [34]. The peak at 993 cm −1 was attributed to the –OH out-of-plane bending vibration [35,36]. A strong and sharp peak was found at 812 cm −1 , which was a characteristic of the triazine ring [37].…”
Section: Resultsmentioning
confidence: 99%
“…Thus, a wide range of adsorbents have been investigated for PFAS elimination from polluted waters. Conventional PFAS adsorbents mainly include activated carbon (AC) 11 , ion exchange resins 12 , minerals 13 , molecularly imprinted polymer (MIP) 14 , biosorbents 15 18 , carbon nanotubes (CNTs) 19 , metal-organic frameworks (MOFs) 20 , and covalent organic frameworks (COFs) 21 . However, these adsorbents often have some limitations including low capacity (0.63 × 10 −3 –753 mg g −1 ) 12 14 , 16 , 20 , long equilibrium time (1–48 h) 11 14 , 20 , weak binding affinity, poor water/chemical stabilities, and low natural organic matter (NOM) selectivity, which limit their practical applications in the treatment of contaminated water 22 , 23 .…”
Section: Introductionmentioning
confidence: 99%
“…Note that HMP shows a peak at 2950 cm −1 that is not present in the melamine spectra; this is attributed to C–H stretching vibrations. In addition, the following are also observed in the HMP spectra: An absorption peak at 3325 cm −1 , which represents amino (–NH 2 ) and amino (–NH–) vibrations [31]; a methylene C–H bending vibration at 1485 cm −1 [32]; and a secondary amine C–N stretching at 1157 cm −1 [33]. All of these findings indicate that melamine reacted with formaldehyde to develop methylol melamine and these methylol melamine further formed a prepolymer with –NH–CH 2 –NH– linkage by a self-condensation reaction (Figure 1b).…”
Section: Resultsmentioning
confidence: 99%