Università degli Studi "Aldo Moro" di Bari, Dip. Chimica, Via Orabona, 4-70126 Bari, Italy.
Consiglio Nazionale delle Ricerche CNR-IPCF, UOS Bari, Via Orabona, 4-70126 Bari, Italy.
Biomolecules. 2019 Oct 5;9(10):571. doi: 10.3390/biom9100571.
This paper reported the first example on the use of chitosan films, without further modification, to remove and recover, through bio-sorption processes, the emerging pollutant Diclofenac from water. The latter was adopted as a model, among non-steroidal anti-inflammatory drugs, by obtaining a maximum adsorption capacity, q, on chitosan of about 10 mg/g, under the applied experimental conditions of work. The literature gap about the use of chitosan films, which was already used for dyes and heavy metals removal, to adsorb emerging pollutants from water was covered, claiming the wide range application of chitosan films to remove a different class of pollutants. Several parameters affecting the Diclofenac adsorption process, such as the pH and ionic strength of solutions containing Diclofenac, the amount of the bio-sorbent and pollutant, and the temperature values, were investigated. The kinetics and the adsorption isotherms, along with the thermodynamic parameters (ΔG°, ΔH°, and ΔS°) were also evaluated. The process occurred very efficiently, and Chitosan/Diclofenac amounts dependent, remove about the 90% of the pollutant, in 2 h, from the tested solutions, through electrostatic interaction involving the carboxylic moiety of Diclofenac and Chitosan amino groups. This finding was confirmed by the pH and salt effects on the bio-sorption process, including swelling measurements of Chitosan films and by FTIR-ATR analysis. In detail, the maximum adsorption was observed at pH 5, when pollutant and Chitosan were negatively and positively charged, respectively. By reducing or increasing the pH around this value, a reduced affinity was observed. Accordingly, the presence of salts retarded the Diclofenac removal screening its charges, which hinders the interaction with Chitosan. The sorption was spontaneous (ΔG° < 0) and endothermic (ΔH° > 0) following the pseudo-second order kinetic model. The process was Diclofenac and Chitosan amount dependent. In addition, the Freundlich and Temkin isotherms well described the process, which showed the heterogeneous character of the process. Experiments of the complete desorption were also performed by using NaCl solutions 0.25 M (like sea water salt concentration) proposing the reuse of the pollutant and the recycling of the bio-sorbent lowering the associated costs. The versatility of the adsorbent was reported by exploring the possibility to induce the Diclofenac light-induced degradation after the adsorption and by-products adsorption onto chitosan films. To emphasize the chitosan capacity of treating water, the removal of another pollutant such as Ketoprofen and the mixture of Diclofenac and Ketoprofen were investigated. In this way, a green and eco-friendly production-pollution prevention technology for removing emerging pollutants from water was presented, which reduced the overall environmental impact. This illustrated experiments both in static and dynamic conditions for potential industrial applications.
本文报道了壳聚糖膜首次用于去除水中新兴污染物双氯芬酸的实例,该过程无需进一步修饰,即可通过生物吸附过程实现。双氯芬酸被选为非甾体抗炎药模型,在实验工作条件下,壳聚糖对其的最大吸附容量 q 约为 10mg/g。该研究填补了壳聚糖膜在吸附水中新兴污染物方面的文献空白,证明了壳聚糖膜在去除不同类型污染物方面具有广泛的应用前景。研究还考察了影响双氯芬酸吸附过程的多个参数,例如含有双氯芬酸的溶液的 pH 值和离子强度、生物吸附剂和污染物的用量以及温度值等。同时还评估了动力学和吸附等温线以及热力学参数(ΔG°、ΔH°和ΔS°)。结果表明,该过程非常高效,壳聚糖/双氯芬酸的用量依赖关系可在 2 小时内从测试溶液中去除约 90%的污染物,这是通过涉及双氯芬酸的羧酸部分和壳聚糖氨基之间的静电相互作用实现的。这一发现得到了 pH 值和盐效应对生物吸附过程的影响的证实,包括壳聚糖膜的溶胀测量和傅里叶变换衰减全反射(FTIR-ATR)分析。具体而言,当污染物和壳聚糖分别带负电荷和正电荷时,最大吸附发生在 pH 值为 5 时。通过降低或增加该值附近的 pH 值,观察到吸附亲和力降低。因此,盐的存在阻碍了双氯芬酸的去除,屏蔽了其电荷,从而阻碍了与壳聚糖的相互作用。吸附是自发的(ΔG°<0)和吸热的(ΔH°>0),符合准二级动力学模型。该过程与双氯芬酸和壳聚糖的用量有关。此外,Freundlich 和 Temkin 等温线很好地描述了该过程,表明该过程具有异质性。还通过使用 0.25 M 的 NaCl 溶液(类似于海水盐浓度)进行了完全解吸实验,提出了再利用污染物和生物吸附剂的可能性,从而降低了相关成本,以实现循环利用。通过探索吸附后诱导双氯芬酸光降解和副产物吸附到壳聚糖膜上的可能性,报道了吸附剂的多功能性。为了强调壳聚糖处理水的能力,还研究了去除另一种污染物如酮洛芬以及双氯芬酸和酮洛芬混合物的情况。通过这种方式,提出了一种从水中去除新兴污染物的绿色环保生产-污染预防技术,从而降低了整体环境影响。这说明了在静态和动态条件下进行实验的潜在工业应用。