[Preparation of fluorescent carbon dots by flow-assisted melt polymerization for tetracycline detection in medical wastewater].

Zi-Wei Liu, Lan-Xiu Ni, Jie Chi, Ying-Xi Qin, Zhen-Jia Shi, Yu Wang, Huang-Zhao Wei, Liang Feng, Cheng-Lin Sun
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The control measures and environmental management of TC pollutants in environmental water samples require precise determination of TC pollutant concentrations. Carbon dots (CDs) are an emerging type of fluorescent material with numerous advantages such as easy preparation, low cost, low toxicity, and good biocompatibility. Consequently, they have attracted widespread attention in the field of TC detection. Herein, we synthesized TE-CDs with good blue-fluorescence performance via flow-assisted melt polymerization using tricarboxylic acid and ethylenediamine as raw precursors. The morphology and structure of the prepared TE-CDs were characterized. The transmission electron microscopy (TEM) results showed that the prepared TE-CDs were well dispersed, with an average diameter of (2.43±0.48) nm. The X-ray diffraction (XRD) results showed that the TE-CDs had an amorphous carbon structure. Infrared spectroscopy and X-ray photoelectron spectroscopy (XPS) characterizations showed that the surface of the TE-CDs was rich in hydrophilic groups, such as amino, hydroxyl, and carboxyl groups, which indicated that TE-CDs had good water solubility and were advantageous for detecting TC in medical wastewater. Subsequently, the optical properties of the TE-CDs were investigated. The fluorescence emission spectra of the TE-CDs were recorded at various excitation wavelengths. The emission spectra of the TE-CDs exhibited excitation wavelength dependence and when the excitation wavelength changes from 300 nm to 400 nm, their fluorescence intensity decreased to varying degrees. The TE-CDs exhibited optimal fluorescence intensity at an excitation wavelength of 368 nm, while the emission wavelength was 448 nm. TC could effectively quench the blue fluorescence of the CDs, and by utilizing this property, the detection of TC concentration could be achieved. After the addition of TC, the fluorescence of the system immediately reached an extreme value, and no significant change was observed within 10 min. An incubation time of 20 s was selected to obtain precise results. Additionally, the TE-CDs exhibited stable fluorescence intensity over a wide pH range. The fluorescence stability of the TE-CDs was investigated, and no significant change in fluorescence intensity was observed after standing for 10 d, indicating that the prepared TE-CDs had excellent fluorescence stability. The fluorescence intensity of the TE-CDs decreased to varying degrees within the range of 2-200 mg/L TC until complete quenching occurred. TC mass concentration in the range of 4-20 mg/L showed a good linear relationship (<i>R</i><sup>2</sup>=0.9978) with the fluorescence quenching intensity of the TE-CDs. The limit of detection was 0.2 mg/L. A preliminary investigation was undertaken to explore the quenching mechanism of the TE-CDs fluorescence by TC. Upon addition of TC, a significant reduction in the fluorescence lifetime of the TE-CDs was observed. During the quenching process, no new substances were observed by UV absorption spectroscopy. Additionally, no significant changes in the <sup>1</sup>H NMR spectra of the TE-CDs were noted before and after the addition of TC, indicating the absence of an interaction between the TE-CDs and TC. Therefore, the quenching mechanism may involve dynamic quenching. The selectivity and anti-interference ability of the developed method were evaluated; in the presence of interfering substances, TC quenched the fluorescence of the TE-CDs, indicating that the TE-CDs had good selectivity and anti-interference performance towards TC. The method was applied to the quantitative detection of TC in medical wastewater, with recoveries of 96.5%-119.8% and relative standard deviations of 0.8%-2.6%. 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引用次数: 0

Abstract

Tetracycline (TC) is one of the most important therapeutic drugs that is widely used in hospitals. However, its harmful effects on human health and various ecosystems cannot be ignored. Owing to its poor metabolic activity and low biodegradability, TC commonly discharges as the parent compound and accumulates readily in sludges and soils by precipitation from wastewater, which can induce the evolution of antibiotic-resistant bacteria; therefore, it has been listed as one of the new pollutants with potential ecotoxicological risk. The control measures and environmental management of TC pollutants in environmental water samples require precise determination of TC pollutant concentrations. Carbon dots (CDs) are an emerging type of fluorescent material with numerous advantages such as easy preparation, low cost, low toxicity, and good biocompatibility. Consequently, they have attracted widespread attention in the field of TC detection. Herein, we synthesized TE-CDs with good blue-fluorescence performance via flow-assisted melt polymerization using tricarboxylic acid and ethylenediamine as raw precursors. The morphology and structure of the prepared TE-CDs were characterized. The transmission electron microscopy (TEM) results showed that the prepared TE-CDs were well dispersed, with an average diameter of (2.43±0.48) nm. The X-ray diffraction (XRD) results showed that the TE-CDs had an amorphous carbon structure. Infrared spectroscopy and X-ray photoelectron spectroscopy (XPS) characterizations showed that the surface of the TE-CDs was rich in hydrophilic groups, such as amino, hydroxyl, and carboxyl groups, which indicated that TE-CDs had good water solubility and were advantageous for detecting TC in medical wastewater. Subsequently, the optical properties of the TE-CDs were investigated. The fluorescence emission spectra of the TE-CDs were recorded at various excitation wavelengths. The emission spectra of the TE-CDs exhibited excitation wavelength dependence and when the excitation wavelength changes from 300 nm to 400 nm, their fluorescence intensity decreased to varying degrees. The TE-CDs exhibited optimal fluorescence intensity at an excitation wavelength of 368 nm, while the emission wavelength was 448 nm. TC could effectively quench the blue fluorescence of the CDs, and by utilizing this property, the detection of TC concentration could be achieved. After the addition of TC, the fluorescence of the system immediately reached an extreme value, and no significant change was observed within 10 min. An incubation time of 20 s was selected to obtain precise results. Additionally, the TE-CDs exhibited stable fluorescence intensity over a wide pH range. The fluorescence stability of the TE-CDs was investigated, and no significant change in fluorescence intensity was observed after standing for 10 d, indicating that the prepared TE-CDs had excellent fluorescence stability. The fluorescence intensity of the TE-CDs decreased to varying degrees within the range of 2-200 mg/L TC until complete quenching occurred. TC mass concentration in the range of 4-20 mg/L showed a good linear relationship (R2=0.9978) with the fluorescence quenching intensity of the TE-CDs. The limit of detection was 0.2 mg/L. A preliminary investigation was undertaken to explore the quenching mechanism of the TE-CDs fluorescence by TC. Upon addition of TC, a significant reduction in the fluorescence lifetime of the TE-CDs was observed. During the quenching process, no new substances were observed by UV absorption spectroscopy. Additionally, no significant changes in the 1H NMR spectra of the TE-CDs were noted before and after the addition of TC, indicating the absence of an interaction between the TE-CDs and TC. Therefore, the quenching mechanism may involve dynamic quenching. The selectivity and anti-interference ability of the developed method were evaluated; in the presence of interfering substances, TC quenched the fluorescence of the TE-CDs, indicating that the TE-CDs had good selectivity and anti-interference performance towards TC. The method was applied to the quantitative detection of TC in medical wastewater, with recoveries of 96.5%-119.8% and relative standard deviations of 0.8%-2.6%. In conclusion, the analytical performance of the proposed method is comparable with that of previously reported detection methods; moreover, the method has the advantages of low operational cost, simple preparation process, time-saving, and good repeatability. Therefore, the TE-CDs can be used as chemical sensors for the detection of TC in medical wastewater and have good practical applications.

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[利用流动辅助熔融聚合法制备荧光碳点,用于检测医疗废水中的四环素】。]
四环素(TC)是医院广泛使用的最重要的治疗药物之一。然而,它对人类健康和各种生态系统的有害影响也不容忽视。由于其代谢活性差、生物降解性低,TC 通常以母体化合物的形式排放,并容易通过废水沉淀在淤泥和土壤中积累,从而诱发抗生素耐药菌的进化,因此已被列为具有潜在生态毒理学风险的新污染物之一。环境水样中 TC 污染物的控制措施和环境管理需要精确测定 TC 污染物的浓度。碳点(CD)是一种新兴的荧光材料,具有制备简单、成本低、毒性小、生物相容性好等诸多优点。因此,碳点在三氯甲烷检测领域受到广泛关注。在此,我们以三羧酸和乙二胺为原料,通过流动辅助熔融聚合法合成了具有良好蓝光性能的 TE-CD。对制备的 TE-CD 的形态和结构进行了表征。透射电子显微镜(TEM)结果表明,制备的 TE-CD 分散良好,平均直径为(2.43±0.48)nm。X 射线衍射(XRD)结果表明 TE-CD 具有无定形碳结构。红外光谱和 X 射线光电子能谱(XPS)表征表明,TE-CD 表面富含亲水基团,如氨基、羟基和羧基,这表明 TE-CD 具有良好的水溶性,有利于检测医疗废水中的 TC。随后,研究了 TE-CD 的光学特性。在不同的激发波长下记录了 TE-CD 的荧光发射光谱。TE-CD 的发射光谱与激发波长有关,当激发波长从 300 纳米变为 400 纳米时,其荧光强度会有不同程度的下降。TE-CD 在激发波长为 368 nm 时的荧光强度最佳,而发射波长为 448 nm。TC 可以有效淬灭 CD 的蓝色荧光,利用这一特性可以实现 TC 浓度的检测。加入 TC 后,系统的荧光立即达到极值,10 分钟内未观察到明显变化。为了获得精确的结果,选择了 20 秒的孵育时间。此外,TE-CD 在很宽的 pH 值范围内都表现出稳定的荧光强度。对 TE-CDs 的荧光稳定性进行了研究,在放置 10 d 后未观察到荧光强度发生显著变化,表明制备的 TE-CDs 具有良好的荧光稳定性。在 2-200 mg/L TC 的范围内,TE-CD 的荧光强度有不同程度的下降,直至完全淬灭。TC 质量浓度在 4-20 mg/L 范围内与 TE-CDs 的荧光淬灭强度呈良好的线性关系(R2=0.9978)。检测限为 0.2 毫克/升。为探索 TC 对 TE-CDs 荧光的淬灭机制,进行了一项初步调查。加入 TC 后,观察到 TE-CDs 的荧光寿命显著缩短。在淬灭过程中,紫外吸收光谱没有观察到新的物质。此外,在添加 TC 前后,TE-CD 的 1H NMR 光谱也没有发生明显变化,这表明 TE-CD 与 TC 之间不存在相互作用。因此,淬灭机制可能涉及动态淬灭。对所建立方法的选择性和抗干扰能力进行了评价;在干扰物质存在的情况下,TC淬灭了TE-CDs的荧光,表明TE-CDs对TC具有良好的选择性和抗干扰性。将该方法应用于医疗废水中三氯乙酸的定量检测,回收率为96.5%-119.8%,相对标准偏差为0.8%-2.6%。总之,该方法的分析性能与之前报道的检测方法相当,而且具有操作成本低、制备工艺简单、省时、重复性好等优点。因此,TE-CD 可作为化学传感器检测医疗废水中的 TC,具有良好的实际应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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