全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Kinetic Studies on Saponification of Poly(ethylene terephthalate) Waste Powder Using Conductivity Measurements

DOI: 10.1155/2014/321560

Full-Text   Cite this paper   Add to My Lib

Abstract:

Conductometric measurement technique has been deployed to study the kinetic behavior during the reaction of poly(ethylene terepthalate) (PET) and NaOH. A laboratory made arrangement with facility of continuous stirring was used to carry out experiments at desired temperature. With conductometry, the determination of kinetic as well as thermodynamic parameters becomes more simple and faster as compared to gravimetry. Chemical kinetics of this reaction shows that it is a second order reaction with reaction rate constant ?g?1?s?1 at 70°C. The specific reaction rates of the saponification reaction in the temperature range at various temperatures (50–80°C) were determined. From the data, thermodynamic parameters such as activation energy, Arrhenius constant (frequency factor), activation enthalpy, activation entropy, and free energy of activation obtained were 54.2?KJ?g?1, ?min?1, 90.8?KJ?g?1, 126.5?JK?1?g?1, and 49.9?KJ?g?1, respectively. 1. Introduction The saponification of poly(ethylene terephthalate) (PET) is one of the known reactions in polymer chemistry and it is represented as an example of pseudofirst order in the literature dealing with chemical kinetics [1, 2]. This reaction has been studied by several investigators at different temperatures using different techniques and reagents. Alcoholysis has been carried out by different workers [3–9]. Hydrolysis of PET gives terephthalic acid (TPA) and ethylene glycol (EG) as a reaction product [10–13]. Aminolysis and methanolysis [14–16] give dimethyl terephthalate (DMT) and terephthalamide as a reaction product. Acid alkali and water hydrolysis of PET waste in organic solvent have been reported by several workers [17–21]. Kinetics of a phase transfer catalyzed alkaline hydrolysis of PET has been studied by Kosmidis et al. [22, 23]. They have used trioctylmethylammonium bromide as phase transfer catalyst. The method is useful because, nowadays, terephthalic acid is replacing dimethyl terephthalate as the main monomer in the industrial production of PET. Chemical recycling of PET has been carried out by Karayannidis and Achilias [24]. They found an effective way for production of secondary value-added materials. Alkaline hydrolysis of PET belongs to relatively frequently investigated reactions. Most often, the course of reaction is studied by gravimetry in withdrawn samples. The error in the kinetic and thermodynamic parameters are more in gravimetry as compared to conductometry. Another disadvantage of this method is high Inplace of labouriosity change time and considerable consumption of chemicals.

References

[1]  S. Mishra, V. S. Zope, and A. S. Goje, “Kinetics and Thermodynamics of Hydrolytic Depolymerization of Poly(ethylene terephthalate) at High Pressure and Temperature,” Journal of Applied Polymer Science, vol. 90, no. 12, pp. 3305–3309, 2003.
[2]  S. Mishra, V. S. Zope, and A. S. Goje, “Kinetic and thermodynamic studies of depolymerisation of poly(ethylene terephthalate) by saponification reaction,” Polymer International, vol. 51, no. 12, pp. 1310–1315, 2002.
[3]  S. Baliga and T. W. Wong, “Depolymerization of poly(ethylene terephthalate) recycled from post-consumer soft-drink bottles,” Journal of Polymer Science Part A: Polymer Chemistry, vol. 27, no. 6, pp. 2071–2082, 1989.
[4]  V. R. Vaidya and V. M. Nadkarni, “Unsaturated polyester resins from poly(ethylene terephthalate) waste. 2. Mechanical and dynamic mechanical properties,” Industrial and Engineering Chemistry Research, vol. 27, pp. 2056–2060, 1988.
[5]  U. R. Vaidya and V. M. Nadkarni, “Unsaturated polyester resins from poly (ethylene terephthalate) waste. 1. Synthesis and characterization,” Industrial & Engineering Chemistry Research, vol. 26, no. 2, pp. 194–198, 1987.
[6]  V. N. Orekov and B. M. Rudenko, Vest Khar’kpolytech Inst., vol. 195, p. 10, 1982.
[7]  A. Sniezko, P. Penczek, and R. Ostrysk, InstIndChemwarsaw pol., Forbe lack, vol. 87, p. 1014, 1981.
[8]  R. D. Leaversuch, “Chemical recycling brings real versatility to solid-waste management,” Modern Plastics, vol. 68, no. 7, pp. 41–43, 1991.
[9]  B. Mikalojezyk, A. Lubawy, M. Djewska, P. Smoczynski, and A. Pozniak, Boebel, 11, pol. Pat. PL 120, 009, 1985.
[10]  J. W. Mandoki, VS patent 4 604 772, 1986.
[11]  D. Paszun and T. Spychaj, “Chemical recycling of poly(ethylene terephthalate),” Industrial & Engineering Chemistry Research, vol. 36, no. 4, pp. 1373–1383, 1997.
[12]  H. K. Reimschuessel, “Poly(ethylene terephthalate) formation. Mechanistic and kinetic aspects of direct esterification process,” Industrial & Engineering Chemistry Product Research and Development, vol. 19, pp. 117–125, 1980.
[13]  J. Otton and S. Ratton, “Investigation of the formation of poly(ethylene terephthalate) with model molecules: Kinetics and mechanism of the catalytic esterification and alcoholysis reactions. I. Carboxylic acid catalysis (monofunctional reactants),” Journal of Polymer Science Polymer Chemistry Edition, vol. 26, p. 2183, 1988.
[14]  . Jacques B, J. Devaux, R. Legras, and E. Nield, “Reactions induced by triphenyl phosphite addition during melt mixing of PET/PBT blends: chromatographic evidence of a molecular weight increase due to the creation of bonds of two different natures,” Polymer, vol. 38, no. 21, pp. 5367–5377, 1997.
[15]  M. E. Cagiao, F. J. B. Calleja, C. Vanderdonckt, and H. G. Zachmann, “Study of the morphology of semicrystalline poly(ethylene terephthalate) by hydrolysis etching,” Polymer, vol. 34, no. 10, pp. 2024–2029, 1993.
[16]  Toray Industries, Japanese patent, 146 567, 1976.
[17]  T. Yoshioka, T. sato, A. Okuwaki, and J. Appl, “Hydrolysis of waste PET by sulfuric acid at 150°C for a chemical recycling,” Journal of Applied Polymer Science, vol. 52, pp. 1353–1355, 1994.
[18]  J. R. Campanelli, M. R. Kamal, and D. G. Cooper, “A kinetic study of the hydrolytic degradation of polyethylene terephthalate at high temperatures,” Journal of Applied Polymer Science, vol. 48, no. 3, pp. 443–451, 1993.
[19]  T. Yoshioka, N. Okayama, and A. Okuwaki, “Kinetics of hydrolysis of PET powder in nitric acid by a modified shrinking-core model,” Industrial and Engineering Chemistry Research, vol. 37, pp. 336–340, 1998.
[20]  T. Yoshioka, T. Motoki, and A. Okuwaki, “Kinetics of hydrolysis of poly(ethylene terephthalate) powder in sulfuric acid by a modified shrinking-core model,” Industrial & Engineering Chemistry Research, vol. 40, pp. 75–79, 2001.
[21]  S. Mishra, A. S. Goje, and V. S. Zope, in Proceedings of the International Conference on Plastic Waste Management and Environment, pp. 163–169, New Delhi, India, 2001.
[22]  V. A. Kosmidis, D. S. Achilias, and G. P. Karayannidis, “Poly(ethylene terephthalate) recycling and recovery of pure terephthalic acid. Kinetics of a phase transfer catalyzed alkaline hydrolysis,” Macromolecular Materials and Engineering, vol. 286, no. 10, pp. 640–647, 2001.
[23]  G. P. Karayannidis, A. P. Chatziavgoustis, and D. S. Achilias, “Poly(ethylene terephthalate) recycling and recovery of pure terephthalic acid by alkaline hydrolysis,” Advances in Polymer Technology, vol. 21, no. 4, pp. 250–259, 2002.
[24]  G. P. Karayannidis and D. S. Achilias, “Chemical recycling of poly(ethylene terephthalate),” Macromolecular Materials and Engineering, vol. 292, no. 2, pp. 128–146, 2007.
[25]  B. R. Puri, L. R. Sharma, and M. S. Pathania, Principles of Physical Chemistry, Vishal Publishing, Jalandhar, India, 2005.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133