Chemosphere · 2020
Towards a comparison between the hybrid ozonation-coagulation (HOC) process using Al- and Fe-based coagulants: Performance and mechanism.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Jin Xin, Liu Yuguo, Wang Yong, Zhang Shaohua, Zhang Weijie, Jin Pengkang, Xu Lu, Shi Xuan, Wang Xiaochang C, Lv Shiwen
Аннотация
In this study, the removal performance of a hybrid ozonation-coagulation (HOC) process using AlCl36H2O (Al-HOC) and FeCl36H2O (Fe-HOC) as coagulants for the treatment of wastewater treatment plant (WWTP) effluent and ibuprofen (IBP) was investigated. Compared with the conventional coagulation process and pre-ozonation-coagulation process, much better organic matter removal performance can be achieved for both the Al-HOC and Fe-HOC processes. The Fe-HOC process showed an obviously higher dissolved organic carbon (DOC) removal efficiency than that of the Al-HOC process. Surface hydroxyl groups were determined to be the active sites in generating OH in the HOC process, and the hydrolysed Fe species possessed a higher content of surface hydroxyl groups than the hydrolysed Al species according to fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectra (XPS) analyses. In addition, the hydrolysed Fe species contained a higher portion of tetrahedral sites that were more likely to be stronger Lewis acid sites to react with ozone to generate OH. Furthermore, peroxone reactions in the HOC process were other possible way to enhance the OH generation, and higher H2O2 generation was observed in the Fe-HOC process due to higher O2- generation. Therefore, better removal performance of the Fe-HOC process can be obtained due to the increased OH generation in the Fe-HOC process.