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Alginate/graphene double network hydrogel has recently been demonstrated as a promising adsorbent for water pollutants. To improve the adsorption capacity of the double network hydrogel, physical and chemical modifications are made to obtain an excellent porous structure and more functional groups. As-modified alginate/graphene double network hydrogel has a higher hydroxyl group content under a higher polyvinyl alcohol content and a higher carboxyl group content with a higher oxidation degree. Moreover, the CO2 produced by CaCO3 is used as pore formation agent avoiding the use of toxic organic matters. The modified alginate/graphene double network hydrogel shows a higher specific surface area, a larger mean pore diameter, and a higher pore volume with a higher initial CaCO3. In antibiotics adsorption, the mechanistic understanding shows that hydrogen bonds have greater influence on adsorption than carboxyl groups. The results reported here pave the way for the use of the alginate/graphene double network hydrogel for water treatment.
This article was published in the following journal.
Name: Journal of colloid and interface science
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Sterile solutions, essentially free from foreign particles and suitably compounded and dispensed, for instillation into the eye. It does not include solutions for cleaning eyeglasses or CONTACT LENS SOLUTIONS. (From Dorland, 27th ed)
Local antibacterial that probably acts by releasing formaldehyde in aqueous solutions. It is used for irrigation of infected body cavities - bladder, peritoneum, etc. and as a spray for burns.
A strong oxidizing agent used in aqueous solution as a ripening agent, bleach, and topical anti-infective. It is relatively unstable and solutions deteriorate over time unless stabilized by the addition of acetanilide or similar organic materials.
An anionic surfactant, usually a mixture of sodium alkyl sulfates, mainly the lauryl; lowers surface tension of aqueous solutions; used as fat emulsifier, wetting agent, detergent in cosmetics, pharmaceuticals and toothpastes; also as research tool in protein biochemistry.
Nonsusceptibility of bacteria to the action of the beta-lactam antibiotics. Mechanisms responsible for beta-lactam resistance may be degradation of antibiotics by BETA-LACTAMASES, failure of antibiotics to penetrate, or low-affinity binding of antibiotics to targets.