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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TQ630

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    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).

    Reference
    [1] BANERJEE G, CHATTOPADHYAY P. Vanillin biotechnology: the perspectives and future[J]. Journal of the Science of Food and Agriculture, 2019, 99(2): 499-506.
    [2] MOTA M I F, PINTO P C R, LOUREIRO J M, et al. Successful recovery and concentration of vanillin and syringaldehyde onto a polymeric adsorbent with ethanol/water solution[J]. Chemical Engineering Journal, 2016, 294: 73-82.
    [3] PRIEFERT H, RABENHORST J, STEINBUCHEL A. Biotechnological production of vanillin[J]. Applied Microbiology and Biotechnology, 2001, 56(3-4): 296-314.
    [4] WALTON N J, NARBAD A, FAULDS C B, et al. Novel approaches to the biosynthesis of vanillin[J]. Current Opinion in Biotechnology, 2000, 11(5): 490-496.
    [5] MUHEIM A, LERCH K. Towards a high-yield bioconversion of ferulic acid to vanillin[J]. Applied Microbiology and Biotechnology, 1999, 51(4): 456-461.
    [6] WANG J X (王建新), JIN B D (金宝德), PENG Q J (彭奇均), et al. Research on the synthesis of vanillin from guaiacol and glyoxylic acid[J]. Fine Chemicals (精细化工), 2000, 17(9):511-514.
    [7] RAO S R, RAVISHANKAR G A. Vanilla flavour: production by conventional and biotechnological routes[J]. Journal of the Science of Food and Agriculture, 2000, 80(3): 289-304.
    [8] GOMES E D, RODRIGUES A E. Recovery of vanillin from kraft lignin depolymerization with water as desorption eluent[J]. Separation and Purification Technology, 2020, 239.
    [9] YUSOF N N M, TANIOKA E, KOBAYASHI T. Molecularly imprinted polymer particles having coordinated hydrogen bonding in covalent-imprinting for efficient recognition towards vanillin[J]. Separation and Purification Technology, 2014, 122: 341-349.
    [10] TARABANKO V E, CHELBINA Y V, KUDRYASHEV A V, et al. Separation of vanillin and syringaldehyde produced from lignins[J]. Separation Science and Technology, 2013, 48(1): 127-132.
    [11] XU X W, LI P H, ZHONG Y D, et al. Review on the oxidative catalysis methods of converting lignin into vanillin[J]. International Journal of Biological Macromolecules, 2023, 243: 125203.
    [12] JI Y C (季迎春), WU Q L (吴菁岚), ZHOU J W (周精卫), et al. Adsorption equilibrium, kinetic and dynamic adsorption of vanillin onto macroporous resin[J]. Chinese Journal of Bioprocess Engineering (生物加工过程), 2018, 16(4): 16-22.
    [13] WANG Z J, CHEN K F, LI J, et al. Separation of vanillin and syringaldehyde from oxygen delignification spent liquor by macroporous resin adsorption[J]. CLEAN - Soil, Air, Water, 2010, 38(11): 1074-1079.
    [14] HUANG Y (黄艳), CHENG G(陈功), WANG R M(王睿猛), et al. Synergistic desorption of low volatile vanillin with ethanol on MIL-100(Fe)[J]. CIESC Journal (化工学报), 2021, 72(5): 2697-2705.
    [15] ZHANG H (张昊), LI Y X (李雅兴), ZHANG Y (张毅), et al. Synthesis of starch-based sulfonic ion exchange resin and its adsorption properties of dyes[J]. Fine Chemicals (精细化工), 2020, 37(1): 135-146.
    [16] TANG W (谭望), GUO X H (郭兴华), ZHANG S (张顺), et al. Synthesis of nitrogen-rich covalent organic framework and its adsorption property for volatile iodine[J]. Scientia Sinica(Chimica)(中国科学:化学), 2019, 49(1): 207-214.
    [17] WANG C L (王昌禄), LI S L (李士炼), ZHOU Q L (周庆礼), et al. Extraction of vanillin in fermented broth by macroporous adsorption resin[J]. Fine Chemicals (精细化工), 2005, 22(6): 458-460.
    [18] GUO P T (郭鹏涛), CHENG X T (成西涛), ZHENG A L (郑阿龙), et al. Synthesis and application progress of hypercrosslinked polymeric adsorbent resin[J]. Applied Chemical Industry (应用化工), 2021, 50(10): 2892-2894+2898.
    [19] MOTA M I F, RODRIGUES PINTO P C, LOUREIRO J M, et al. Recovery of vanillin and syringaldehyde from lignin oxidation: a review of separation and purification processes[J]. Separation Purification Reviews, 2015, 45(3): 227-259.
    [20] XU M C (徐满才), SHI Z Q (史作清), HE B L (何炳林). Synthesis, structures and properties of hypercrosslinked polystyrene adsorbents[J]. Ion Exchange and Adsorption (离子交换与吸附), 1994, 10(6): 555-562.
    [21] Zheng J Y, Hu L, He X D, et al. Evaluation of pore structure of polarity-controllable post-cross-linked adsorption resins on the adsorption performance of 5-hydroxymethylfurfural in both single- and ternary-component systems[J]. Industrial Engineering Chemistry Research, 2020, 59(39): 17575-17586.
    [22] CAO Z N (曹志农), WEI J (韦嘉), YAN J (严俊). Postcrosslinking of macroporous st-dvb copolymer in the presence of carbon tetrachloride[J]. Acta Polymerica Sinica (高分子学报), 2002(04), 452-456.
    [23] Jin X Y, Huang J H. Adsorption of vanillin by an anisole-modified hyper-cross-linked polystyrene resin from aqueous solution: equilibrium, kinetics, and dynamics[J]. Advances in Polymer Technology, 2013, 32(S1): E221-E230.
    [24] LANGMUIR I. The constitution and fundamental properties of solids and liquids. Part I. Solids[J]. Journal of the American Chemical Society, 1916, 38(11): 2221-2295.
    [25] FREUNDLICH H. über die adsorption in l?sungen[J]. Zeitschrift für Physikalische Chemie, 1907, 57U(1): 385-470.
    [26] ZHENG K, PAN B C, ZHANG Q J, et al. Enhanced adsorption of p-nitroaniline from water by a carboxylated polymeric adsorbent[J]. Separation and Purification Technology, 2007, 57(2): 250-256.
    [27] EDER S, MULLER K, AZZARI P, et al. Mass transfer mechanism and equilibrium modelling of hydroxytyrosol adsorption on olive pit-derived activated carbon[J]. Chemical Engineering Journal, 2021, 404: 126519.
    [28] MANES M, HOFER L J. Application of the Polanyi adsorption potential theory to adsorption from solution on activated carbon[J]. The Journal of Physical Chemistry, 1969, 73(3): 584-590.
    [29] LAGERGREN S K. About the theory of so-called adsorption of soluble substances[J]. Sven Vetenskapsakad Handingarl, 1898, 24(4): 1-39.
    [30] HO Y S, MCKAY G. Kinetic models for the sorption of dye from aqueous solution by wood[J]. Process Safety and Environmental Protection, 1998, 76(2): 183-191.
    [31] WEBER WALTER J, MORRIS J C. Kinetics of adsorption on carbon from solution[J]. Journal of the sanitary engineering division, 1963, 89(2): 31-59.
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History
  • Received:November 17,2023
  • Revised:March 26,2024
  • Adopted:February 20,2024
  • Online: December 10,2024
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