Benssassi Mohamed El Hadi, Dali Awatef, Sehili Tahar, Ustun-Odabasi Sevde, Harakat Dominique
Laboratoire des Sciences et Technologies de l'Environnement (LSTE), Faculté des Sciences Exactes, Université des Frères Mentouri Constantine 1, 25000, Constantine, Algeria.
Faculty of Process Engineering, University Constantine 3 Salah Boubnider, Constantine, Algeria.
Environ Sci Pollut Res Int. 2025 Jan;32(2):833-848. doi: 10.1007/s11356-024-35820-3. Epub 2024 Dec 20.
In this study, the photodegradation of cetirizine dihydrochloride (CET) by BiO/TiO heterojunctions under simulated solar light irradiation (300-800nm) was examined in detail for the first time. A hydrothermal synthesis of the photocatalyst was carried out, and several analytical techniques were used to characterize the product. The resulting BiO/TiO photocatalyst effectively removed CET from an aqueous solution. The BiO/TiO (5.0%/95.0%) ratio exhibited the highest photocatalytic performance for CET degradation, degrading 75.85% of CET after 60 min of irradiation, with a high pseudo-first-order rate constant (k = 0.022 min; t = 31.50 min; natural pH). Moreover, TOC decreased by 40.45% after 420 min of irradiation. The BiO/TiO photocatalyst has also been proven effective in degrading CET in different real aqueous matrices (Seawater (99.89%) > spring water (68.44%) > tap water (52.62%)), and the degradation under natural solar irradiation is more effective and faster than under artificial irradiation. Additionally, the BiO/TiO photocatalyst demonstrated excellent photo-stability in a five-cycle photocatalytic experiment. The influence of various parameters showed that the removal of CET was heightened with a dose of 1 g/L of the BiO/TiO and enhanced under acidic conditions (pH = 2.3). Moreover, the involvement of different reactive species was investigated by introducing diverse scavengers, revealing that hydroxyl radicals and photo-holes were the main reactive species involved in the CET photodegradation process over the BiO/TiO photocatalyst. The primary photodegradation byproducts were identified using HPLC-MS analysis, and a possible mechanism was proposed.
在本研究中,首次详细考察了BiO/TiO异质结在模拟太阳光照射(300 - 800nm)下对盐酸西替利嗪(CET)的光降解作用。进行了光催化剂的水热合成,并使用多种分析技术对产物进行表征。所得的BiO/TiO光催化剂能有效从水溶液中去除CET。BiO/TiO(5.0%/95.0%)比例对CET降解表现出最高的光催化性能,照射60分钟后降解了75.85%的CET,具有较高的准一级速率常数(k = 0.022 min⁻¹;t₁/₂ = 31.50 min;自然pH)。此外,照射420分钟后总有机碳(TOC)降低了40.45%。BiO/TiO光催化剂在不同的实际水体基质中降解CET也被证明是有效的(海水(99.89%)>泉水(68.44%)>自来水(52.62%)),并且在自然太阳光照射下的降解比人工照射更有效、更快。此外,BiO/TiO光催化剂在五循环光催化实验中表现出优异的光稳定性。各种参数的影响表明,BiO/TiO投加量为1 g/L时对CET的去除效果增强,且在酸性条件(pH = 2.3)下效果更佳。此外,通过引入不同的清除剂研究了不同活性物种的参与情况,结果表明羟基自由基和光生空穴是BiO/TiO光催化剂上CET光降解过程中的主要活性物种。使用高效液相色谱 - 质谱(HPLC - MS)分析鉴定了主要光降解副产物,并提出了可能的机理。