超高交联吸附树脂的制备及其对香草醛的吸附性能
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广东工业大学 轻工化工学院

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TQ630

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国家自然科学基金(21978053,51508547);广东省重点领域研发计划项目(2020B0101070001)


Preparation of hyper-cross-linked adsorption resin and its adsorption characteristics of vanillin
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School of Chemical Engineering Light Industry,Guangdong University of#$NBSTechnology

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    摘要:

    以悬浮聚合法和悬挂双键后交联法为基础,选用不同的制孔剂,制备出四种不同的树脂作为香草醛的吸附介质。其中由甲苯作制孔剂制备的PCL-PDE树脂吸附香草醛的性能最佳。以PCL-PDE树脂作为吸附介质系统地研究了其在单组份香草醛水溶液中的静态吸附行为。在吸附温度为25℃、初始浓度为1.0 g/L的条件下,PCL-PDE树脂对香草醛的吸附容量高达80.0 mg/g(湿树脂)。动力学结果表明,PCL-PDE树脂吸附香草醛是一个先快后慢的过程,最后在180 min内达到平衡。Langmuir吸附模型拟合的最高吸附容量为240.4 mg/g,Freundlich吸附模型拟合的指数n均大于1,说明该吸附是优惠性吸附。热力学参数表明,该吸附过程是一个自发的放热过程(ΔG<0,ΔH<0)。关键词:香草醛;吸附;超高交联吸附树脂;动力学;热力学中图分类号:TQ630 文献标识码: A 文章编号:1003-5214 (2020) 01-0000-00

    Abstract:

    Four different resins were prepared as adsorption medium for vanillin based on suspension polymerization and post-suspension double bond crosslinking, and different pore-making agents were used. The results showed that the PCL-PDE resin prepared from toluene as the pore-making agent has the best performance in the adsorption of vanillin. The static adsorption behavior of vanillin in single component aqueous solutions on the resin was systematically investigated using PCL-PDE resin as the adsorption medium. The adsorption capacity of PCL-PDE resin for vanillin was as high as 80.0 mg/g (wet resin) at an adsorption temperature of 25 °C and an initial concentration of 1.0 g/L. Kinetic studies showed that the adsorption of vanillin by PCL-PDE resin was a fast and then slow process, reaching equilibrium within 180 min. The highest adsorption capacity fitted by the Langmuir adsorption model was 240.4 mg/g, and the exponents n fitted by the Freundlich adsorption model were all greater than 1, indicating that the adsorption was preferential. The thermodynamic calculations showed that the adsorption process was a spontaneous exothermic process (ΔG < 0, ΔH < 0).

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邱全源,胡蕾,曾越任,刘泾柯,宋九航,林晓清.超高交联吸附树脂的制备及其对香草醛的吸附性能[J].精细化工,2024,41(12):

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  • 收稿日期:2023-11-17
  • 最后修改日期:2024-03-26
  • 录用日期:2024-02-20
  • 在线发布日期: 2024-12-10
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