卟啉锌金属有机骨架室温催化降解阿莫西林抗生素的形态结构研究

IF 1.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Advances in Materials Science Pub Date : 2021-07-13 DOI:10.11648/J.AM.20211002.12
S. Saxena, Punya Saluja, J. Krishna, T. Basu
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引用次数: 0

摘要

过去几十年来,环境中持久性和生物活性微污染物的大量增加。由于大多数临床模式充斥着抗生素,污水处理废水、地表水和二次排水等环境样本显示世界范围内存在生物顽固性抗生素,因此抗生素耐药微生物的数量急剧上升。为了避免阿莫西林浓度的上升(微克/升),我们设计了一个潜在的金属有机框架(MOF),并对其催化功能进行了实验室测试。以四(4-羧基苯基)卟啉H2TCPP(>97%)为配体,乙酸锌为金属盐,溶剂热合成了锌-卟啉MOF。利用FESEM、XRD、EDAX、FTIR和uv -可见光谱对其进行了形貌和结构表征。制备的MOF催化剂在室温黑暗环境下具有良好的降解阿莫西林的能力,在0.1 mg/ml浓度下,其降解效率约为97.3%。催化剂暴露于抗生素90分钟显示最大的降解,之后阿莫西林浓度没有进一步变化。我们首次利用电化学循环伏安(CV)测量来监测降解过程,并通过FTIR记录验证,并注意到降解过程遵循一级动力学。我们还讨论了制备的锌卟啉MOF在抗生素暴露后的形态稳定性,并报道了不同MOF种类催化效率的比较大纲。高孔隙率和羧基苯基卟啉配体在Zn+2空位d轨道上的有效电荷转移是室温下有效吸附和降解阿莫西林抗生素的关键因素。我们期望所开发的锌卟啉MOF由于其能量效率(暗)和有效降解抗生素的简单过程而具有成功的商业应用前景。
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Morphological and Structural Elucidation of Room Temperature Catalytic Degradation of Amoxicillin Antibiotic Using Zinc Porphyrin Metal Organic Framework
Environment is witnessing an extensive increase in persistent and bioactive micro pollutants from the last few decades. Since most clinical modalities are flooded with antibiotics, environmental samples such as sewage treatment effluents, surface water and secondary water drainage etc. reveal the presence of bio-recalcitrant antibiotics worldwide, ergo there is a spurring rise in antibiotic resistant microorganisms. In order to circumvent the escalating concentration of amoxicillin (microgram/liter) we contrived a potential metal organic framework (MOF) and lab tested it for catalytic functionality. A zinc-porphyrin MOF using Tetra (4-carboxyphenyl) porphyrin H2TCPP (>97%) as a ligand and Zinc acetate as a metal salt was solvo-thermally synthesized. The morphological and structural characterization were performed using FESEM, XRD, EDAX, FTIR and UV-Visible spectroscopy. The fabricated MOF catalyst exhibits sterling ability of amoxicillin degradation in a dark environment at room temperature, accounting a degradation efficiency of about 97.3% in a 0.1 mg/ml concentration. 90 minutes of catalyst exposure to the antibiotic shows maximum degradation after which there is no further change in amoxicillin concentration. First time we have exploited electrochemical cyclic voltametric (CV) measurement to monitor the degradation process which was validated by FTIR recording, and noticed that the degradation process followed a first order kinetics. We have also discussed the morphological stability of the fabricated Zn porphyrin MOF after antibiotic exposure and reported a comparative outline between catalytic efficiency of different MOF species. High porosity and effective charge transfer between carboxyphenyl) porphyrin ligand to vacant d orbital of Zn+2 are pivotal factors for effective sorption and degradation of amoxicillin antibiotics dark at room temperature. We would expect the developed Zn porphyrin MOF is very promising for successful commercial application due to its energy efficiency (dark) and simple process for effective degradation of antibiotics.
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Advances in Materials Science
Advances in Materials Science MATERIALS SCIENCE, MULTIDISCIPLINARY-
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