2008
DOI: 10.1016/j.carbpol.2007.11.009
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Ionic interactions between sulfuric acid and chitosan membranes

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Cited by 126 publications
(78 citation statements)
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“…Genipine and tripolyphosphate (TPP) have been applied in this sense with a great deal of emphasis [16]. Studies have shown the use of sulfuric acid as a crosslinking agent to be applied as materials for proton exchange and evaporation, as studied by Devi et al [17] and Cui et al [18]. However, its application in the biomedical field, until the present moment, has not been studied yet for biomedical applications.…”
Section: Introductionmentioning
confidence: 99%
“…Genipine and tripolyphosphate (TPP) have been applied in this sense with a great deal of emphasis [16]. Studies have shown the use of sulfuric acid as a crosslinking agent to be applied as materials for proton exchange and evaporation, as studied by Devi et al [17] and Cui et al [18]. However, its application in the biomedical field, until the present moment, has not been studied yet for biomedical applications.…”
Section: Introductionmentioning
confidence: 99%
“…Chitosan (beta-(1,4)-2-amino-2-deoxy-d-glucose) is a low cost N-deacetylated product of chitin. Since CS contains active amino groups and hydroxyl groups that can form hydrogen bonds with water, in the past decades, chitosan has been well recognized as a very promising hydrophilic material for pervaporation membranes and construction of functional films [2,3,7,9,[20][21][22][23][24][25][26]. In this paper, the CS complex membranes were formed under a dynamic filtration process.…”
Section: Introductionmentioning
confidence: 99%
“…The sulfonation of the C 2 amino groups by concentrated H 2 SO 4 solutions occurs in two steps: the amino groups of chitosan are firstly protonated by H 2 SO 4 ; then a SO 4 2-anion interacts with two NH 3 + groups to form ionic bridges between them. 21,22 Therefore, the sulfonation at the C 2 amino groups can also realize the crosslinking of chitosan. The sulfonation reaction of the C 6 hydroxyl groups is illustrated in Fig.…”
Section: Synthesis Mechanism Of Sccrmentioning
confidence: 99%
“…The peak at 1260 cm -1 is attributed to the S=O bond, and that at 802 cm -1 corresponds to the C-O-S bond, indicating the formation of C 6 -O sulfate ester. [21][22][23] Moreover, the characteristic adsorptions of the primary alcoholic C-O bond and glycoside bond in the saccharide ring are overlapped into a broad peak be-…”
mentioning
confidence: 99%