首页|NTA-Fe@PDA/H2O2氧化去除废水中盐酸土霉素

NTA-Fe@PDA/H2O2氧化去除废水中盐酸土霉素

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利用聚多巴胺(PDA)与氮川三乙酸(NTA)接枝并螯合Fe3+,形成以PDA为载体、NTA为Fe3+螯合剂的芬顿催化剂NTA-Fe@PDA,采用NTA-Fe@PDA/H2O2芬顿氧化法去除废水中盐酸土霉素(OTC)。材料表征结果发现,NTA-Fe@PDA属于典型的介孔结构,Fe元素与有机配体成功螯合,PDA的聚合效果良好。探讨了 H2O2投加量、NTA-Fe@PDA投加量和初始pH值对OTC降解的影响。结果表明,在NTA-Fe@PDA浓度为200mg/L,H2O2浓度为5mmol/L,初始pH值为4。85的条件下,反应60min后,20mg/L OTC的降解率达到96。23%。自由基鉴定实验表明,·OH是OTC降解过程中的主要自由基。通过LC-MS分析结果推测了 OTC降解的中间产物和可能的降解路径。NTA-Fe@PDA在反应体系中重复利用8次以后,OTC的降解率仍在86。80%以上。NTA-Fe@PDA/H2O2芬顿法为抗生素废水处理提供了一种新思路和技术参考。
NTA-Fe@PDA/H2O2 oxidation for removal of oxytetracycline hydrochloride from wastewater
In this paper,polydopamine(PDA)grafted with nitrilotriacetic acid(NTA)and Fe3+were chelated to form Fenton catalyst.Advanced oxidation process of NTA-Fe@PDA activated H2O2 was used to remove oxytetracyclin hydrochloride(OTC)from wastewater.The material characterization analysis showed that NTA-Fe@PDA was a typical mesoporous structure,Fe successfully chelated with organic ligand,and the polymerization effect of PDA was good.The effects of H2O2 dosage,NTA-Fe@PDA dosage and initial pH value on the degradation of OTC were investigated.Experimental results indicated that the degradation rate of 20mg/L OTC reached 96.23%after reaction for 60min,under the conditions of 5mmol/L H2O2,200mg/L NTA-Fe@PDA and initial pH 4.85.Free radical quenching experiments confirmed that·OH was the main free radical for OTC degradation.The possible degradation path of OTC was inferred by LC-MS analysis.The degradation rate of OTC was still above 86.80%after NTA-Fe@PDA was reused for 8times.Fenton oxidation process of NTA-Fe@PDA provided a new idea and technical reference for the treatment of antibiotic wastewater.

polydopamine(PDA)Fe3+chelating agentFenton oxidationoxytetracycline hydrochloride(OTC)degradation mechanism

林嘉伟、苏冰琴、李兴发、卫月星、郑晓晓、张霞玲、宋鑫峂、赵文博

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太原理工大学环境科学与工程学院,山西 晋中 030600

山西省市政工程研究生教育创新中心,山西 晋中 030600

聚多巴胺 Fe3+螯合剂 芬顿氧化 盐酸土霉素 降解机制

山西省自然科学基金国家自然科学基金

2021030212317422206149

2024

中国环境科学
中国环境科学学会

中国环境科学

CSTPCDCHSSCD北大核心
影响因子:2.174
ISSN:1000-6923
年,卷(期):2024.44(5)