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• W2895979576 abstract "Abstract Struvite crystallization is one of the most promising routes for phosphorus recovery from phosphorus-rich sludge. However, the adsorption of alginic acid, a surrogate of extracellular polymeric substances in phosphorus-rich sludge, on struvite crystals has been proved to significantly inhibit struvite crystallization. To comprehensively understand the inhibitory mechanism, the adsorption behavior was evaluated at various adsorption time, the concentration of alginic acid, pH and ionic strength in the present study. Subsequently, adsorption equilibrium isotherm, kinetic and thermodynamics models were employed to fit the adsorption data. Interestingly, the adsorption mechanism was explored by X-ray photoelectron spectra (XPS) and Fourier transform infrared spectroscopy analysis (FTIR), which was further elucidated by triple-layer model (TLM). The results indicated that the adsorption capacity of struvite crystals almost reached a plateau value within the first 30 min. Meanwhile, the adsorption capacity was significantly reduced with increasing pH, but slightly increased with increasing ionic strength. Moreover, the adsorption process obeyed pseudo-second order kinetic model and Langmuir adsorption isotherm model, whereas intra-particle diffusion was a main rate-limited step. Furthermore, hydrogen bonding and surface complexation between alginic acid and struvite crystals dominated the adsorption mechanism. Additionally, alginic acid underwent surface reactions by virtue of two outer-sphere surface complexes and one inner-sphere surface complex. The findings presented herein will facilitate understanding of the inhibitory mechanism of organic matters on struvite crystallization from phosphorus-rich sludge." @default.
• W2895979576 created "2018-10-26" @default.
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• W2895979576 date "2019-02-01" @default.
• W2895979576 modified "2023-10-02" @default.
• W2895979576 title "New insights into the adsorption behavior and mechanism of alginic acid onto struvite crystals" @default.
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• W2895979576 doi "https://doi.org/10.1016/j.cej.2018.10.110" @default.
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