2018
DOI: 10.1098/rsos.171927
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Preparation of chitosan/MCM-41-PAA nanocomposites and the adsorption behaviour of Hg(II) ions

Abstract: A novel functional hybrid mesoporous composite material (CMP) based on chitosan and MCM-41-PAA was reported and its application as an excellent adsorbent for Hg(II) ions was also investigated. Innovatively, MCM-41-PAA was prepared by using diatomite and polyacrylic acid (PAA) with integrated polymer–silica hybrid frameworks, and then CMP was fabricated by introducing MCM-41-PAA to chitosan using glutaraldehyde as a cross-linking agent. The structure and morphology of CMP were characterized by X-ray diffraction… Show more

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Cited by 19 publications
(3 citation statements)
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“…This occurs through the exchange or sharing of electrons between sunset yellow, indigo carmine, titan yellow, and orange G dye, and the functional groups present in the SBA-15/polypyrrole composite. [25][26][27] This is also in accordance with the results from 3.8.1 (ii) in the work, which suggests that the possible mechanism of dyes involves electrostatic interactions between the SBA-15/polypyrrole composite and dye molecules.…”
Section: Pseudo-second-order Modelsupporting
confidence: 91%
“…This occurs through the exchange or sharing of electrons between sunset yellow, indigo carmine, titan yellow, and orange G dye, and the functional groups present in the SBA-15/polypyrrole composite. [25][26][27] This is also in accordance with the results from 3.8.1 (ii) in the work, which suggests that the possible mechanism of dyes involves electrostatic interactions between the SBA-15/polypyrrole composite and dye molecules.…”
Section: Pseudo-second-order Modelsupporting
confidence: 91%
“…Cross-linked poly(acrylic acid)—p(AA) particles are examples of nanogels sensitive to pH. Due to the presence of a high amount of carboxylic groups, pAA gels undergo a big-volume transition in response to appropriate pH changes [18]. At pH smaller than p K a of pAA (4.5) [19], they exist in the shrunken state (carboxylic groups are protonated), while at pH higher than p K a they are swollen (carboxylic groups are dissociated).…”
Section: Introductionmentioning
confidence: 99%
“…have many applications in drug release [8][9][10][11][12][13][14][15][16][17] (for more details regarding the application of chitosan and its derivatives in drug release, see review, [18] and references therein), biological activity [19][20][21][22][23][24] (for more details regarding the biological activity of chitosan and its derivatives, see review, [25] and references therein)), beverages and food industry [26][27][28][29] (also see [30] and references therein, an extensive review reporting the application of chitosan and its derivatives in beverages and food industry) as well as membranes for the removal of various pollutants such as metals, ions, dyes, pharmaceuticals/drugs, phenols, pesticides, herbicides, etc. [31][32][33][34][35][36][37][38][39][40][41][42][43][44] (references [31] and [44] are extensive reviews).…”
Section: Introductionmentioning
confidence: 99%