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Modified Macroporous Adsorption Resins With Amino and Acetyl Groups Through a Novel Method and Adsorption Behaviors for Alizarin Yellow GG

机译:一种新颖的氨基和乙酰基改性大孔吸附树脂及其对茜素黄GG的吸附行为

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摘要

Under bubble with air compressor, macroporous adsorption resin was functionalized with amino and acetyl groups. The method avoided the fragmentation of the resin during modification. Alizarin yellow GG (AYGG) was used as an adsorbate to investigate adsorption kinetics of the modified resins. It showed that pseudofirst-order and pseudosecond-order kinetics cannot reasonably express the adsorption process. A new kinetic model, multi-layer adsorption model, showed much better fit to the adsorption kinetic data and corresponding kinetic parameters could predict adsorption mechanism. Meantime, AYGG can be easily recovered, and the resins can be regenerated. Due to n-n, electrostatic force and hydrogen bond interaction between the resin and car-boxyl, phenolic hydroxyl, and azo groups of AYGG, the resin with amino group showed higher adsorption capacity than the other resins used in this study. Steric hindrance and decrease in electrostatic force were unfavorable for the enrichment of AYGG by the resin with acetyl group. Response surface model combining with central composite design was used to determine effects of pH and initial concentration on adsorption. It showed that a second-order polynomial regression model could reasonably express the experimental data and optimum adsorption conditions were obtained. The design provided an effective methodology to optimize an adsorption process.
机译:在空气压缩机的鼓泡下,大孔吸附树脂被氨基和乙酰基官能化。该方法避免了改性期间树脂的碎裂。茜素黄GG(AYGG)被用作吸附物以研究改性树脂的吸附动力学。结果表明,伪一级和伪二级动力学不能合理地表示吸附过程。一个新的动力学模型,即多层吸附模型,显示出对吸附动力学数据的更好拟合,并且相应的动力学参数可以预测吸附机理。同时,AYGG可以容易地回收,并且树脂可以再生。由于AYGG的羧基,羧基,酚羟基和偶氮基团之间存在n-n,静电力和氢键相互作用,因此带有氨基的树脂比本研究中使用的其他树脂具有更高的吸附能力。立体位阻和静电力的降低不利于带有乙酰基的树脂对AYGG的富集。响应表面模型与中心复合材料设计相结合,用于确定pH和初始浓度对吸附的影响。结果表明,二阶多项式回归模型可以合理地表达实验数据,并获得了最佳的吸附条件。该设计提供了一种有效的方法来优化吸附过程。

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