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首页> 外文期刊>Environmental Engineering Science >Adsorption of Fluoxetine and Venlafaxine onto the Marine Seaweed Bifurcaria bifurcata
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Adsorption of Fluoxetine and Venlafaxine onto the Marine Seaweed Bifurcaria bifurcata

机译:氟西汀和文拉法辛在海洋紫菜双歧杆菌上的吸附

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摘要

Marine macroalga Bifurcaria bifurcata was investigated as sorbent for two environmental emerging pollutants, the pharmaceuticals venlafaxine (VLF) and fluoxetine (FLX), from aqueous solutions, both in mono and bi-component batch systems. The alga was characterized by means of IR spectroscopy, allowing to identify the most important groups for biosorption, carboxylic, sulfonic and hidroxile. The point of zero charge was determined, being 6.4. Adsorption of FLX follows a pseudo first order kinetics and kinetic constants are higher for FLX than for VLF. Its adsorption better represented by the pseudo second order model. For both pharmaceuticals, the equilibrium was reached within similar to 100 min. Adsorption studies reveal that the process was more efficient at lower pH range and followed the Langmuir-Freundlich's model for VLF and Langmuir's model for FLX. Maximum adsorption capacities reached a level of 12 +/- 3 and 22 +/- 4 mu mol/g for VLF and FLX, respectively, in the mono-component system. The difference was attributed to the presence of various functional groups of varying polarity within the adsorbates' molecules that affected their interactions with the adsorbent surface. The Langmuir-Freundlich's extended model was applied to the adsorption data of the bi-component system and no changes in the maximum adsorption capacities were found (14 +/- 2 and 20 +/- 3 mu mol/g for VLF and FLX, respectively), there is no evidence of competition between the adsorbates.
机译:研究了海洋大型藻类双歧双歧杆菌(Bifurcaria bifurcata)作为单组分和双组分分批系统中水溶液中两种环境新兴污染物(药物文拉法辛(VLF)和氟西汀(FLX))的吸附剂。通过红外光谱对藻类进行了表征,从而可以鉴定出最重要的生物吸附基团,即羧基,磺酸基和Hidroxile。确定零电荷点为6.4。 FLX的吸附遵循伪一级动力学,并且FLX的动力学常数高于VLF。假二阶模型较好地表示了它的吸附。对于两种药物,均在约100分钟内达到平衡。吸附研究表明,该工艺在较低的pH范围内更有效,并且遵循Langmuir-Freundlich VLF模型和Langmuir FLX模型。在单组分系统中,VLF和FLX的最大吸附容量分别达到12 +/- 3和22 +/- 4μmol/ g。差异归因于被吸附物分子中存在极性不同的各种官能团,这些官能团影响它们与吸附剂表面的相互作用。将Langmuir-Freundlich扩展模型应用于双组分系统的吸附数据,未发现最大吸附容量发生变化(VLF和FLX分别为14 +/- 2和20 +/- 3μmol / g) ),没有证据表明被吸附物之间存在竞争。

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