Suppr超能文献

使用石英晶体微天平对聚酰胺薄膜在氯和过氧乙酸水溶液中的降解动力学进行比较研究。

Comparative Degradation Kinetics Study of Polyamide Thin Films in Aqueous Solutions of Chlorine and Peracetic Acid Using Quartz Crystal Microbalance.

作者信息

Mohona Tashfia M, Dai Ning, Nalam Prathima C

机构信息

Department of Civil, Structural and Environmental Engineering, University at Buffalo, Buffalo, New York 14260, United States.

Department of Materials Design and Innovation, University at Buffalo, Buffalo, New York 14260, United States.

出版信息

Langmuir. 2021 Dec 7;37(48):14214-14227. doi: 10.1021/acs.langmuir.1c02835. Epub 2021 Nov 18.

Abstract

Polyamide thin film composite membranes are widely used in water reclamation. Peracetic acid (PAA) is an emerging wastewater disinfectant with a potential for membrane cleaning and disinfection; however, its interaction with polyamide remains poorly understood. This study employs quartz crystal microbalance with dissipation (QCM-D) to determine the PAA-induced degradation kinetics of polyamide thin films, in comparison with the conventional disinfectant-free chlorine (HOCl). Polyamide films showed a sorption phase followed by a degradation phase when exposed to PAA (1000 mg L) and HOCl (100 mg L) solutions. While the sorption phase in HOCl experiments was short (1.4-3.5 min) and followed a Boltzmann-sigmoidal model, it spanned over 3-33 h in PAA experiments and displayed a two-stage behavior. The latter kinetics are attributed to sequential processes of the physical sorption of PAA in polyamide films followed by PAA-induced polyamide oxidation. In the degradation phase, the HOCl-exposed films followed a rapid, two-step exponential decay reaching an equilibrium mass of ∼50% of the initial (wet) mass after ∼5 h of exposure. In contrast, the PAA-exposed films followed a Boltzmann-sigmoidal decay, with ∼80% of the initial (wet) mass remaining intact after >10 h of exposure. Fast force maps generated using atomic force microscopy showed a progressive increase in the morphological heterogeneity of the polyamide films in HOCl solution due to pitting, cracking, bulging, and eventual delamination under both flow and no-flow conditions. In contrast, PAA only formed small pits on the polyamide film under flow; in a stagnant PAA solution, the film had no visible changes even after ∼148 h of exposure. This is the first comparative study on the chemical and morphological changes in polyamide films induced by PAA and HOCl. The much higher compatibility of polyamide with PAA than with chlorine supports the potential of PAA being used as a halogen-free membrane cleaning/disinfecting agent.

摘要

聚酰胺复合薄膜广泛应用于水回收领域。过氧乙酸(PAA)是一种新兴的废水消毒剂,具有膜清洗和消毒的潜力;然而,其与聚酰胺的相互作用仍知之甚少。本研究采用带耗散监测的石英晶体微天平(QCM-D)来测定PAA诱导的聚酰胺薄膜降解动力学,并与传统消毒剂游离氯(HOCl)进行比较。当聚酰胺薄膜暴露于PAA(1000 mg/L)和HOCl(100 mg/L)溶液时,呈现出一个吸附阶段,随后是降解阶段。虽然HOCl实验中的吸附阶段较短(1.4 - 3.5分钟),且符合玻尔兹曼 - 西格莫伊德模型,但在PAA实验中,该阶段持续3 - 33小时,并呈现出两阶段行为。后一种动力学归因于PAA在聚酰胺薄膜中的物理吸附以及随后PAA诱导的聚酰胺氧化的连续过程。在降解阶段,暴露于HOCl的薄膜呈现快速的两步指数衰减,暴露约5小时后达到平衡质量,约为初始(湿)质量的50%。相比之下,暴露于PAA的薄膜呈现玻尔兹曼 - 西格莫伊德衰减,暴露超过10小时后,约80%的初始(湿)质量保持完整。使用原子力显微镜生成的快速力图谱显示,在流动和非流动条件下,由于点蚀、开裂、鼓包以及最终分层,HOCl溶液中聚酰胺薄膜的形态异质性逐渐增加。相比之下,PAA在流动条件下仅在聚酰胺薄膜上形成小坑;在静止的PAA溶液中,即使暴露约148小时后,薄膜也没有明显变化。这是第一项关于PAA和HOCl诱导的聚酰胺薄膜化学和形态变化的比较研究。聚酰胺与PAA的兼容性远高于与氯的兼容性,这支持了PAA作为无卤膜清洗/消毒剂的潜力。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验