1998
DOI: 10.1002/cjce.5450760214
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Enhancement of the retention performance of the poly(ethylene oxide) — tannic acid system by poly (diallyldimethyl ammonium chloride)

Abstract: The retention performance of the poly(ethy1ene oxide) (PEO) and tannic acid (TA) dual system was studied in the presence of poly(diallyldimethyl ammonium chloride) (PDADMAC). The zeta potential, and size of the association complex between PEO and TA in the presence of PDADMAC as well as the infrared spectra of TA and the PEO-TA system were also studied. It was shown that hydrogen bonds are formed between the phenolic and acidic groups of TA and the oxygen atoms of the PEO macromolecules. Moreover, it was found… Show more

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Cited by 14 publications
(8 citation statements)
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“…In addition, there was an increment in the C=O vibration in TA, which was changed from 1713 cm −1 (free TA) to 1739 cm −1 (TA in complex) [27], which indicates an interaction between the C=O of the Cu (CH 3 COO) 2 and the O-H groups of TA, as a hydrogen donors. These two types of chemical energy shifts shown in FT-IR were similar to previous reported studies [23,28], which confirms that both the C=O and -OH found in TA are key elements for the complex formation.…”
Section: Surface Composition Analysissupporting
confidence: 90%
“…In addition, there was an increment in the C=O vibration in TA, which was changed from 1713 cm −1 (free TA) to 1739 cm −1 (TA in complex) [27], which indicates an interaction between the C=O of the Cu (CH 3 COO) 2 and the O-H groups of TA, as a hydrogen donors. These two types of chemical energy shifts shown in FT-IR were similar to previous reported studies [23,28], which confirms that both the C=O and -OH found in TA are key elements for the complex formation.…”
Section: Surface Composition Analysissupporting
confidence: 90%
“…However, these shifts turned into one peak at 3430 cm −1 for the adhesive, revealing transformation of the free hydroxyls into associated H-bonds. 64 For the physical mixture of PEG and TA powders, there existed unbound hydroxyl groups and weak H-bonds by appearance of the shifts at 3518, 3580, and 3430 cm −1 . After forming the PEG/TA adhesive, the strong stretching vibration of −CH 2 at 2872 cm −1 and CO at 1740 cm −1 shifted to peaks of 2903 and 1724 cm −1 , respectively, which ascribed to the steric effect caused by the formed H-bonds.…”
Section: ■ Results and Discussionmentioning
confidence: 97%
“…At the well-defined region of −OH attributed to 3300–3600 cm –1 , the shifts of 3518 and 3580 cm –1 in PEG-SG and 3622 cm –1 in TA were assigned to free or unbound −OH. However, these shifts turned into one peak at 3430 cm –1 for the adhesive, revealing transformation of the free hydroxyls into associated H-bonds . For the physical mixture of PEG and TA powders, there existed unbound hydroxyl groups and weak H-bonds by appearance of the shifts at 3518, 3580, and 3430 cm –1 .…”
Section: Results and Discussionmentioning
confidence: 99%
“…All these changes show the intermolecular interaction between TA and PEG via hydrogen bonds. 16,22 Meanwhile, the adhesive force of TAPE was dependent on the molar ratio of pyrogallol in TA and the terminal −OH of PEGs in TAPE (Figure 1d). As the pyrogallol ratio to the hydroxyl group of PEG increased, enhancement of adhesive force was observed.…”
Section: ■ Results and Discussionmentioning
confidence: 97%