The usage of a highly efficient, low-cost, and sustainable adsorbent material as an industrial wastewater treatment technique is required. Herein, the usage of the novel, fully sustainable tannin-5-(hydroxymethyl)furfural (TH) aerogels, generated via a water-based sol-gel process, as compatible biosorbent materials is presented. In particular, this study focusses on the surface modification of the tannin biosorbent with carboxyl or amino functional groups, which, hence, alters the accessible adsorption sites, resulting in increased adsorption capacity, as well as investigating the optimal pH conditions for the adsorption process. Precisely, highest adsorption capacities are acquired for the metal cations and cationic dye in an alkaline aqueous environment using a carboxyl-functionalized tannin biosorbent, whereas the anionic dye requires an acidic environment using an amino-functionalized tannin biosorbent. Under these determined optimal conditions, the maximum monolayer adsorption capacity of the tannin biosorbent ensues in the following order: Cu > RB > Zn > MO, with 500, 244, 192, 131 mg g, respectively, indicating comparable or even superior adsorption capacities compared to conventional activated carbons or silica adsorbents. Thus, these functionalized, fully sustainable, inexpensive tannin biosorbent materials, that feature high porosity and high specific surface areas, are ideal industrial candidates for the versatile adsorption process from contaminated (heavy) metal or dye solutions.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10606356PMC
http://dx.doi.org/10.3390/gels9100822DOI Listing

Publication Analysis

Top Keywords

tannin biosorbent
20
fully sustainable
8
biosorbent materials
8
adsorption capacity
8
optimal conditions
8
adsorption process
8
adsorption capacities
8
adsorption
7
biosorbent
6
tannin
5

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!