Instituto de Química, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9500 Porto Alegre, RS, Brazil.
Instituto de Química, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9500 Porto Alegre, RS, Brazil.
Sci Total Environ. 2020 Nov 15;743:140629. doi: 10.1016/j.scitotenv.2020.140629. Epub 2020 Jul 4.
A tube-in-tube membrane reactor, with radial addition of hydrogen peroxide, was used for the oxidation of four pharmaceuticals, paracetamol (PCT), furosemide (FRS), nimesulide (NMD), and diazepam (DZP), in a continuous-mode operation, using photochemical and photocatalytic processes, driven by UVA or UVC photons. This reactor allows a controlled titration of small HO doses (inside-out mode) to the catalyst particles immobilized in the membrane shell side and to the annular space between the membrane inner tubing and the concentric outer quartz tubing, where water to be treated flows. Tests were performed using synthetic (SWW) and real (urban wastewater after secondary treatment) (UWW) matrices, both spiked with the pharmaceutical mix solution (200 μg L of each). The photochemical and photocatalytic oxidation efficiency was evaluated as a function of HO dose (5-20 mg L), oxidant injection mode (radial permeation vs injection upstream from the reactor inlet), light source (UVA vs UVC lamps) and aqueous matrix (synthetic vs real matrix). At steady-state regime, the UVC/HO/TiO system, with radial HO addition (20 mg L), showed the highest pharmaceuticals removal percentage, PCT (27.4%), FRS (35.0%), NMD (24.2%) and DZP (30.0%) in SWW. A substantial decrease in pharmaceuticals elimination was observed for UWW (PCT - 11.5%, FRS - 20.3%, NMD - 8.2% and DZP - 12.6%), in comparison with the SWW matrix. Finally, twelve transformation products (TPs) were identified; most of them showed in their structures hydroxylation in aromatic moiety; all TPs chemical structures were evaluated by BIOWIN software indicating that the TPs are non-biodegradables.
管式膜反应器,采用过氧化氢径向添加方式,在连续操作模式下,使用光化学和光催化过程,利用 UVA 或 UVC 光子,氧化四种药物,对乙酰氨基酚(PCT)、呋塞米(FRS)、尼美舒利(NMD)和地西泮(DZP)。该反应器允许对固定在膜壳侧的催化剂颗粒和膜内管与同心外石英管之间的环形空间中(待处理的水流动)的小 HO 剂量(内向外模式)进行受控滴定。使用合成(SWW)和实际(二级处理后的城市废水)(UWW)基质进行了测试,均用药物混合溶液(每种 200μg/L)进行了加标。评估了 HO 剂量(5-20mg/L)、氧化剂注入方式(径向渗透与反应器入口上游注入)、光源(UVA 与 UVC 灯)和水基质(合成与实际基质)对光化学和光催化氧化效率的影响。在稳态下,采用径向添加 HO(20mg/L)的 UVC/HO/TiO 系统,在 SWW 中对药物的去除率最高,PCT(27.4%)、FRS(35.0%)、NMD(24.2%)和 DZP(30.0%)。与 SWW 基质相比,UWW 中药物消除率大幅下降(PCT-11.5%、FRS-20.3%、NMD-8.2%和 DZP-12.6%)。最后,鉴定出 12 种转化产物(TPs);它们的结构大多显示芳族部分的羟化;所有 TPs 的化学结构均通过 BIOWIN 软件进行了评估,表明 TPs 不可生物降解。