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ACS Applied Materials & Interfaces · 2025 · IF 8.2

Enhancing Biodegradation of Insoluble High Molecular Weight Polycyclic Aromatic Hydrocarbons in Macroemulsion (ME) Bioreactors with a Liquid–Liquid Interface

Ke Han,Rui Li,Yule Lu,Xin Sun,Jie Cui,Yin-Zhu Wang,Yong Wang,Hao Lv,Yonghong Hu,Li Mi

Due to the low bioavailability and insolubility of high molecular weight polycyclic aromatic hydrocarbons (HMW-PAHs) in aqueous solutions, their degradation efficiency is significantly limited in wastewater treatment and environmental remediation. To address this challenge, we designed oil-in-water (O/W) macroemulsion (ME) bioreactors with mixed surfactants (Tween-80 and Triton X-100), n-butanol, corn oil, and Burkholderia vietnamiensis (BVs) to enhance the degradation efficiency of pyrene. Owing to the higher solubility of pyrene in MEs, it could be easily adsorbed onto hydrophobic groups on the cell surface. Furthermore, the fluorescence images showed that the BVs were adsorbed on the surface of the MEs, increasing the contact frequency and interactions between pyrene and BVs. Meanwhile, the degradation efficiency of the prepared ME bioreactor was improved by up to 198% compared to that of the conventional surfactant. Therefore, the constructed ME bioreactors can provide green guidance for HMW-PAH biodegradation in industrial wastewater and environmental remediation.

CAS / MDL: 7385-67-3 129-00-0
研究领域: 环境科学 · 微生物学
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RSC Advances · 2016 ·Vol. 6 ·期 91 ·88701-88706 · IF 3.289

In situ charge neutralization on governing particle coagulation nucleation and size distribution in macroemulsion polymerization

B. J. Liu,W. T. Meng,M. Y. Zhang,H. X. Zhang

Fabricating monodispersed polymer latex particles with ∼300 nm size at high monomer concentrations by batch macroemulsion polymerization remains significantly challenging because of latex stability. In this study, we developed a novel approach based on in situ charge neutralization to prepare 40 wt% solid content latex containing monodispersed sub-300 nm latex particles. The cationic initiator 2,2′-azobis(2-methylpropionamidine)dihydrochloride (AIBA) was used to induce in situ charge neutralization in the particle nucleation period and shield the negative charges of surfactant sodium dodecyl sulfate molecules to further reduce the electrostatic repulsion between primary particles, resulting in primary particle coagulation nucleation. The primary particle coagulation promoted particle number decreased to ∼1016 L−1, and the average particle size increased to ∼100 nm at a very low monomer conversion (<0.12). With increasing AIBA concentrations from 0.6 and 0.8 to 1.0 wt% (the molar ratio of AIBA/SDS is 0.64, 0.85 and 1.06, respective), the average particle size of the latex ultimately attained from 170.6 and 221.7 to 288.0 nm, respectively. Moreover, the addition of an electrolyte and copolymerization composition also governed the particle coagulation extent and affected the particle size distribution of the ultimate latex particles. To the best of our knowledge, this is the simplest, most efficient, and inexpensive approach to prepare large sized, monodispersed latex particles.

研究领域: 化学工程 · 材料科学
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