Tantuvoy Sonam, Bose Saptarshi, Ghosh Alakananda, Kumar Satvir, Kumar Mathava
Environmental Engineering Division, Department of Civil Engineering, Indian Institute of Technology Madras, Chennai, Tamil Nadu, 600036, India.
Environmental Engineering Division, Department of Civil Engineering, Indian Institute of Technology Madras, Chennai, Tamil Nadu, 600036, India.
J Environ Manage. 2025 Jan;373:123772. doi: 10.1016/j.jenvman.2024.123772. Epub 2024 Dec 24.
The release of toxic chemical dyes from the industrial effluent poses huge challenges for the environmental engineers to treat it. Azo dyes encompass the huge part of textile discharges which are difficult to degrade due to their complex chemical aromatic structures and due to the presence of strong bonds (-N=N-). Thus, the removal of a carcinogenic azo dye (i.e., malachite green (MG)), via microwave (MW) - assisted technology in the presence of spinel cobalt ferrite (CoFeO) catalyst was investigated. The synthesized CoFeO nanoparticles were characterized via XRD, FTIR, TGA, VSM, and SEM-EDAX analytical techniques. The nanoparticles were found to be spherical (17.42 nm), and crystalline in nature. The impact of MW power (300-700W), MW temperature (60°- 90 °C), CoFeO dosage (0-1.2 g/L), and initial MG dye concentrations (15-100 mg/L) on MG removal were studied. The maximum MG decolorization (>90%) was observed within 2 min, and the remaining decolorization was completed within next 3 min under the optimized condition. The reaction rates were significantly boosted by MW irradiation, resulting in faster MG degradation with pseudo second-order kinetics rate (R ∼ 0.99). The MW irradiation would induce the localised hotspot zones over the catalytic surface, thus promoting the reactive radical species generation, which targeted the organic pollutant achieving the higher degree of mineralization (TOC∼90%). The toxicity reduction after the MW treatment suggests that the bulky toxic aromatic chains of the dye compound might have fragmented into simpler, smaller, and less toxic compounds. The ⦁OH played a major role in the degradation of MG dye through demethylation, elimination of benzene rings, and subsequent mineralization to CO, and HO. No detectable leaching of cobalt (Co) metal was observed from the catalyst, which ensured the stability of Co in the catalyst. Moreover, CoFeO was recovered easily after the MW treatment via external magnetic separation, due to its high saturation magnetization value (i.e., 59.5 emu/g). Additionally, cost incurred for dye removal via MW irradiation was compared ($ 308 per kg of the dye pollutant removed) with several other processes, and found on economic side in comparison. According to the findings, the microwave irradiation process assisted by CoFeO treatment offers a practical, and potential approach for treating dye laden wastewater, along with the easier catalyst retrieval mechanism using magnetism.
工业废水中有毒化学染料的排放给环境工程师处理废水带来了巨大挑战。偶氮染料占纺织废水的很大一部分,由于其复杂的化学芳香结构以及存在强键(-N=N-),难以降解。因此,研究了在尖晶石钴铁氧体(CoFeO)催化剂存在下,通过微波(MW)辅助技术去除致癌偶氮染料(即孔雀石绿(MG))。通过XRD、FTIR、TGA、VSM和SEM-EDAX分析技术对合成的CoFeO纳米颗粒进行了表征。发现这些纳米颗粒呈球形(17.42纳米),且为晶体。研究了微波功率(300-700W)、微波温度(60°-90°C)、CoFeO用量(0-1.2g/L)和初始MG染料浓度(15-100mg/L)对MG去除的影响。在优化条件下,2分钟内观察到最大MG脱色率(>90%),接下来3分钟内完成其余脱色。微波辐射显著提高了反应速率,导致MG以准二级动力学速率更快降解(R∼0.99)。微波辐射会在催化表面诱导局部热点区域,从而促进活性自由基的产生,这些自由基靶向有机污染物,实现更高程度的矿化(TOC∼90%)。微波处理后毒性降低表明,染料化合物庞大的有毒芳香链可能已分解为更简单、更小且毒性更低的化合物。⦁OH在MG染料的降解中起主要作用,通过脱甲基、消除苯环以及随后矿化为CO和HO。未观察到催化剂中有可检测到的钴(Co)金属浸出,这确保了催化剂中Co的稳定性。此外,由于CoFeO具有高饱和磁化值(即59.5emu/g),微波处理后通过外部磁分离很容易回收。此外,将通过微波辐射去除染料的成本(每去除1kg染料污染物308美元)与其他几种工艺进行了比较,发现从经济角度来看具有优势。根据研究结果,CoFeO处理辅助的微波辐射工艺为处理含染料废水提供了一种实用且有潜力的方法,同时具有利用磁性更易于回收催化剂的机制。