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用于从模拟废水中去除蛋白胨的双木质素衍生聚合物体系。

Dual lignin-derived polymeric system for peptone removal from simulated wastewater.

作者信息

Wang Yingchao, Wang Qiang, Sabaghi Sanaz, Kaboli Afrouz, Soltani Farshid, Kang Kang, Kongvarhodom Chutima, Fatehi Pedram

机构信息

State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology (Shandong Academy of Sciences), Jinan, Shandong, 250353, China; Green Processes Research Centre and Chemical Engineering Department, Lakehead University, 955 Oliver Road, Thunder Bay, ON, P7B 5E1, Canada.

State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology (Shandong Academy of Sciences), Jinan, Shandong, 250353, China.

出版信息

Environ Pollut. 2024 Feb 15;343:123142. doi: 10.1016/j.envpol.2023.123142. Epub 2023 Dec 22.

Abstract

The long-term existence of peptone can breed a large number of bacteria and cause the eutrophication of municipal wastewater. Thus, removing peptone in the wastewater is a major challenge facing the current industry. This study used cationic and anionic lignin polymers, i.e., kraft lignin-[2-(methacryloyloxy)ethyl] trimethylammonium methyl sulfate (cationic lignin polymer, CLP) and kraft lignin-acrylic acid (anionic lignin polymer, ALP), as flocculants to eliminate peptone from model wastewater in the single and dual component systems. The affinity of peptone for ALP or CLP was assessed by quartz crystal microbalance with dissipation, X-ray photoelectron spectroscopy, contact angle, and vertical scan analyzer. Results illustrated that the adsorption effect of CLP for peptone was significantly superior to that of ALP owing to the stronger vital interaction between cationic polymer and peptone molecules. Based on destabilization and sedimentation analyses, introducing CLP triggered the preliminary flocculation of peptone via bridging action, as indicated by a considerable increment in the destabilization index (from 1.1 to 10.6). Moreover, peptone adsorbed more on the CLP coated surface than on the ALP coated one (14.8 vs 5.4 mg/m), while ALP facilitated its further adsorption in the dual polymer system. This is because CLP adsorbed a part of peptone molecules on its surface. Then, ALP entrapped the unattached peptone onto the CLP coated surface through electrostatic interaction. Compared with the single polymer system, mixing ALP and CLP subsequently into the peptone solution in the dual system generated larger size aggregates (mean diameter of 6.1 μm) and made the system destabilization (Turbiscan stability index up to 58.1), thereby yielding more flocculation and sedimentation. Finally, peptone was removed successfully from simulated wastewater with a turbidity removal efficiency of 92.5%. These findings confirmed that the dual-component system containing two lignin-derived polymers with opposite charges could be viable for treating peptone wastewater.

摘要

蛋白胨的长期存在会滋生大量细菌,导致城市污水富营养化。因此,去除污水中的蛋白胨是当前行业面临的一项重大挑战。本研究使用阳离子和阴离子木质素聚合物,即硫酸盐木质素-[2-(甲基丙烯酰氧基)乙基]三甲基铵(阳离子木质素聚合物,CLP)和硫酸盐木质素-丙烯酸(阴离子木质素聚合物,ALP),作为絮凝剂,在单组分和双组分系统中从模拟废水中去除蛋白胨。通过具有耗散功能的石英晶体微天平、X射线光电子能谱、接触角和垂直扫描分析仪评估蛋白胨对ALP或CLP的亲和力。结果表明,由于阳离子聚合物与蛋白胨分子之间更强的重要相互作用,CLP对蛋白胨的吸附效果明显优于ALP。基于失稳和沉降分析,引入CLP通过架桥作用引发蛋白胨的初步絮凝,失稳指数显著增加(从1.1增至10.6)表明了这一点。此外,蛋白胨在CLP包覆的表面上比在ALP包覆的表面上吸附更多(14.8对5.4mg/m),而ALP在双聚合物系统中促进其进一步吸附。这是因为CLP在其表面吸附了一部分蛋白胨分子。然后,ALP通过静电相互作用将未附着的蛋白胨捕获到CLP包覆的表面上。与单聚合物系统相比,在双系统中随后将ALP和CLP混合到蛋白胨溶液中会产生更大尺寸的聚集体(平均直径为6.1μm),并使系统失稳(Turbiscan稳定性指数高达58.1),从而产生更多的絮凝和沉降。最后,成功从模拟废水中去除了蛋白胨,浊度去除效率达到92.5%。这些发现证实,含有两种带相反电荷的木质素衍生聚合物的双组分系统可用于处理蛋白胨废水。

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