This study reports on the highly simple fabrication of green carbon black (GCB) generated from scrap tires with acetic acid to improve the adsorption efficiency for water purification, which is thoroughly compared with conventional carbon black (CB) obtained from petrochemicals. Unlike traditional modification processes with strong acids or bases, the introduction of a relatively mild acid readily allowed for the effective modification of GCB to increase the uptake capability of metal ions and toxic organic dyes to serve as effective adsorbents. The morphological features and thermal decomposition patterns were examined by electron microscopy and thermogravimetric analysis (TGA). The surface functional groups were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The structural information (ratio of D-defects/G band-graphitic domains) obtained by Raman spectroscopy clearly suggested the successful fabrication of GCB (ID/IG ratio of 0.74), which was distinctively different from typical CB (ID/IG ratio of 0.91). In the modified GCB, the specific surface area (SBET) gradually increased with the reduction of pore size as a function of acetic acid content (52.97 m2/g for CB, 86.64 m2/g for GCB, 102.10-119.50 m2/g for acid-treated GCB). The uptake capability of the modified GCB (312.5 mg/g) for metal ions and organic dyes was greater than that of the unmodified GCB (161.3 mg/g) and typical CB (181.8 mg/g), presumably due to the presence of adsorbed acid. Upon testing them as adsorbents in an aqueous solution, all these carbon materials followed the Langmuir isotherm over the Freundlich model. In addition, the removal rates of cationic species (>70% removal of Cu2+ and crystal violet in 30 min) were much faster and far greater than those of anionic metanil yellow (<40% removal in 3 h), given the strong electrostatic interactions. Thus, this work demonstrates the possibility of recycling waste tires in the powder form of GCB as a cost-effective and green adsorbent that can potentially substitute traditional CB, and the modification strategy provides a proof of concept for developing simple fabrication guidelines of other carbonaceous materials.
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Rapid Adsorption of Cationic Methylene Blue Dye onto Volcanic Ash‑metakaolin Based Geopolymers
In this study, four geopolymer sorbents GP0, GP10, GP30 and GP50 were synthesized using volcanic ash (VA) and metakaolin (MK) blends as precursors with 0, 10, 30 and 50% MK content by mass, respectively. The materials were characterized by X-ray fuorescence (XRF), X-ray difraction (XRD), Raman spectroscopy, and Brunauer–Emmett–Teller (BET) surface area analyses, revealing successful geopolymerization of the precursors and increasing surface area with increasing MK content. The sorption performance of the VA, MK and VA-MK geopolymers was then evaluated for the removal of cationic methylene blue (MB) dye from aqueous media. Sorption capacity was independent of composition, providing fexibility in sorbent synthesis. Sorption rate, on the other hand, was 3–8 times greater for the VA-MK geopolymers than the precursor materials. The equilibrium adsorption data were suitably explained by the Freundlich model, denoting multilayer adsorption onto a heterogeneous adsorption surface with higher Freundlich afnity constant (KF) for geopolymers than VA. The adsorption kinetics obeyed the pseudo-second-order (PSO) kinetic law with an average of 98% removal efciency in 30 min. MB uptake was pH-dependent and driven by electrostatic chemisorption interactions. These results motivate further studies on the use of locally sourced geopolymers for water purifcation applications.
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- Award ID(s):
- 2032590
- PAR ID:
- 10342225
- Date Published:
- Journal Name:
- Silicon
- ISSN:
- 1876-9918
- Page Range / eLocation ID:
- 1-11
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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