Adsorption Separation of Various Polar Dyes in Water by Oil Sludge-Based Porous Carbon

Autor: Huanquan Cheng, Longgui Peng, Jia Liu, Cuiying Ma, Fangtao Hao, Bin Zheng, Jianye Yang
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: Applied Sciences, Vol 14, Iss 16, p 7283 (2024)
Druh dokumentu: article
ISSN: 2076-3417
DOI: 10.3390/app14167283
Popis: The pollution caused by printing and dyeing wastewater is increasingly severe, posing significant harm to aquatic plants and animals. In this study, porous carbon was synthesized via the high-temperature pyrolysis of light and heavy organic matter present in oily sludge, utilizing low oil content sludge as the raw material and zinc chloride as a chemical activator. The results exhibited a significant increase in the specific surface area of the oily sludge-based porous carbon, from 4.95 m²/g to 10.95 m²/g. The effects of various parameters such as pH, amount of sorbent, dye concentration, temperature, and contact time on dye removal have been studied. The results showed that the oil sludge-based porous carbon exhibited high efficiency in removing Malachite Green from aqueous solutions, which has low polarity and remains consistently above 97%. The removal rate of Crystal Violet, which is more polar, was as low as 24.14%. The corresponding adsorption capacities were 33.41 mg/g for Malachite Green, 16.41 mg/g for Crystal Violet, and 13.56 mg/g for Methylene Blue. The adsorption capacity of OSC700 for three types of dyes was characterized by monolayer adsorption, primarily driven by chemical adsorption, with significant contributions from electrostatic and hydrophobic effects. The adsorption process was spontaneous, exothermic, and accompanied by an increase in entropy. For less polar substances, the adsorption on oily sludge-based porous carbon is primarily driven by aromatic functional groups on the carbon surface, hydrophobicity, π-π electron-donor-acceptor (π-π EDA) interactions, and surface hydrogen bond formation. In contrast, for more polar dyes, electrostatic and hydrophobic interactions dominate, with electrostatic adsorption being the predominant mechanism and minimal hydrogen bond formation during adsorption.
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