Research Article | Open Access
Dilip B. Patil, Vijendra Batra, Sushil B. Kapoor, "Kinetic Studies on Saponification of Poly(ethylene terephthalate) Waste Powder Using Conductivity Measurements", Journal of Polymers, vol. 2014, Article ID 321560, 7 pages, 2014. https://doi.org/10.1155/2014/321560
Kinetic Studies on Saponification of Poly(ethylene terephthalate) Waste Powder Using Conductivity Measurements
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.
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 . 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.
Hence, in the present work, an online conductivity measurement is carried out to evaluate the second order reaction rate constants with possibly lowest experimental error for saponification of PET waste powder in order to obtain information about activation energy, activation enthalpy, activation entropy, and free energy of activation.
All chemicals used in the present work were of analytical reagent grade. The solution of NaOH was prepared using conductivity water. PET waste bottles were procured from local corporation area of Nagpur, Maharashtra state, India. The bottles were dipped into the solution of Teepol and then washed using double distilled water. Finally, washed with high-purity water having Millipore water conductivity less than 1 µs cm−1. All the bottles were dried with hot air blower. The cleaned and dried bottles were chilled to increase their brittleness, then, crushed, ground, and sieved into different particle sizes ranging from 800 to 100 µm.
The optimum parameters for saponification of PET waste powder were determined by gravimetric measurements. PET waste powder (2–12 g) was taken into 100 mL of conductivity water containing (4–10 g) of sodium hydroxide, and 3 mL of pyridine was added to keep the reaction mixture at pH 14. The reaction mixture was refluxed at 50–80°C for 150 minutes in 250 mL three-vertical-neck round bottom flask equipped with a reflux water condenser, microcontroller based stirrer, and internal digital temperature measurement probe. After 150 min, the cooled reaction mixture was filtered to separate PET powder residue and sodium salt of TPA. The salt was precipitated with stoichiometric amount of HCl. A white precipitate of TPA, after complete removal of chloride ions, was vacuum dried at 90°C for 2 h. The product obtained by saponification was characterized by instrumental analysis such as FTIR spectra (Figure 1). FTIR spectra of product were compared to standard TPA spectra (Figure 2). The optimum parameters determined were further used for the kinetic measurement using conductometry.
In kinetic measurements, three-vertical-neck round bottom flask was fixed with refluxed water condenser, an internal digital temperature measurement probe, a conductivity measuring cell, and microcontroller based vertical type of stirrer. The conductivity cell used was a vertical Teflon probe with platinum electrodes. The cell constant of the cell was about unity. It was cleaned with hydrochloric acid solution and ensured its platinized layer of platinum black before being used. The cell was treated with water or reaction mixture in which PET waste was saponified to give similar concentrations of ions as in the kinetic measurements. A conductivity measurement was made by using a digital conductivity meter made up of Equiptronic India Ltd. Since the aim of the work is to determine kinetic and thermodynamic parameters, the temperature stability and its measurement are important. High precision thermostat and digital temperature measurement probe were used in the present work (Figure 3).
Kinetic experiments were carried out at optimum parameters to determine the rate constant. 10 g PET waste powder (100 µm) and 3 mL of pyridine were added into the reaction flask placed in thermostat. Here, pyridine does not play any role in the kinetics. It maintains the reaction mixture at pH 14. The platinized electrode surfaces of the conductivity measuring cell and tip of the temperature probe were adjusted so that they are not struck by the vertical stirrer bar (Figure 3). 7 g sodium hydroxide in 100 mL conductivity water was placed in the separate 250 mL beaker in the thermostat to the desired reaction temperature. When the thermal equilibrium has been reached, sodium hydroxide solution was added to PET waste powder containing pyridine. Immediately, stopwatch was started. Online conductance of the reaction mixture was measured at various time intervals up to 150 min. is the conductance of conductivity water and , , and are the conductance of reaction mixture at times zero, , and infinity, respectively. From these, the values of and were determined then and . Where is the amount of PET depolymerized at zero time, is the amount of PET depolymerized at time “” and “” is the initial amount of PET. Therefore for second order reaction if plot values (ordinate) against time , is a straight line, rate constant can be deduced from the slope.
The order of reaction was determined by varying the amount of sodium hydroxide and PET waste powder in the reaction mixture. In both cases, rate constant was determined.
In order to evaluate kinetic and thermodynamic parameters, rate constant determinations were also carried out at various temperatures ranging from 50°C to 80°C. From the results, activation energy, frequency factor, activation entropy, activation enthalpy, and free energy of activation were evaluated.
3. Results and Discussion
Saponification of PET waste powder was carried out using various amounts of PET waste powder, sodium hydroxide, and particle size. The saponification was also studied at different temperatures. The results of the optimum saponification parameters are shown in Table 1. These parameters are used to study the kinetics. Conductometric kinetics of saponification of PET waste powder was undertaken on the basis of the hydroxide ion and terephthalate formed in the reaction product. The reaction product was analyzed by FTIR spectra. The FTIR spectra of pure TPA and TPA obtained by saponification reaction were recorded. The FTIR in Figures 1 and 2 shows that the product obtained from saponification of PET waste powder has the same characteristic peaks as pure TPA. The peaks corresponding to aromatic rings are at wave numbers of 700 cm−1 and 800 cm−1, while the peaks corresponding to carboxylic groups are at wave numbers 1730–1650 cm−1. The peak at 3540 cm−1 is for hydroxyl end group and the peak at 3200 cm−1 is for carbonyl overtone. This suggests that the obtained product is TPA because its spectra are similar to those of pure TPA.
The rate constant of saponification was determined by online conductivity measurements at various time intervals. With progress of reaction, highly conducting OH- ions in the reaction mixture were replaced by an identical number of very less conducting terepthalate ions, resulting in continuous decrease in conductivity of the reaction mixture. From the start of the reaction, the decrease in conductivity was continuously monitored online using conductivity meter. The conductivity values at each 25 min. interval of time were recorded. In each case, conductivity contributed by conductivity water () was deducted and corrected conductivity values were recorded. At infinity time, both reactants, PET and NaOH, are completely converted to sodium terephthalate and ethylene glycol as a reaction product. Hence, the specific conductance at infinity time () was recorded by measuring conductivity of reaction product after prolonged period of six hours. The conductivity of the product in the reaction vessel is governed only by sodium terephthalate since ethylene glycol does not contribute to conductivity change (Scheme 1). As shown in Scheme 1, each chain breaking utilizes two sodium hydroxide molecules to form one each of sodium terephthalate and ethylene glycol. Therefore, the progress of the reaction was studied by measuring the conductivity of the sodium hydroxide over a definite reaction time.
The specific conductivity of reaction mixture before the start of reaction, that is, at zero time (), and at various reaction times () during the course of reaction was measured. The specific conductivity of conductivity water () was deducted from the specific conductivity at zero time () and from various reaction times () to get corrected values of and . With the help of corrected values of and , the values of were calculated. The values of were obtained by deducting the conductivity at infinity time (). From these values of and at various reaction times, the values of were evaluated (Table 2). A plot of shows a straight line passing through origin and indicates the second order kinetics (Figure 4). The slope of this plot gives the reaction rate constant. The reaction rate constant is 2.88 × 10−3 g−1s−1 at 70°C. The reaction rate constant was determined by varying the PET waste powder (in grams) and NaOH (in grams). It is observed that the reaction rate constant changes with change in amount of PET waste powder and NaOH each. This confirms the second order nature of this saponification reaction as the concentration of PET waste power and NaOH affects the saponification above and below 10 g of PET and 7 g of NaOH.
|Slope of the graph of versus time = reaction rate constant, = 2.88 × 10−3 g−1s−1.|
The saponification of PET waste powder was also studied at temperature ranging from 50°C to 80°C. The reaction rate constant at these range were determined from the respective slope of the plot are presented in Table 3 and Figure 5. It is observed that, in some cases, the plot intercepts at instead of passing through origin, as expected theoretically.
|Slope of the graph of verses = −2829 K.|
Activation energy: = 54.2 KJg−1.
The presence of such a small intersect may be due to difficulties arising in determining the specific conductivity at zero time () at higher temperature. The Arrhenius plot was also plotted using the values of versus (Table 3 and Figure 6). The slope of the curve is −2829 K, from which activation energy obtained was 54.2 KJg−1. The Arrhenius constant was determined using the formula , where = reaction rate constant at temperature , = activation energy, = gas constant, and = Arrhenius constant. The Arrhenius constant evaluated was Min−1. The other thermodynamic parameters in the saponification reaction of PET and NaOH, such as activation enthalpy, activation entropy, and free energy of activation, were evaluated by Eyring-Polanyi equation  using reaction rate constant at various temperatures. A plot of versus was plotted and, from the slope and intercept of the curve, activation enthalpy obtained was −90.8 KJg−1, while the activation entropy was 126.5 JK−1g−1. From these two values, free energy of activation obtained was 49.9 KJg−1. (Table 4 and Figure 7).
|Slope of the graph of verses = −10925.92.|
Intercept of verses = −4.90.
∴ Activation enthalpy: = −90.8 KJg−1.
Activation energy: = 126.5 JK−1g−1.
Free energy of activation: = 49.9 KJg−1.
To ensure the reliability in the kinetic and thermodynamic parameters, we conducted experiments six times at each temperature. Using these data of reaction rate constant at different temperature, the thermodynamic parameters were determined and shown in Table 5. The results show excellent agreement with these thermodynamic parameters with relative standard deviation from 0.8% to 1.5%.
|Activation energy : 54.2 ± 0.7 kJg−1.|
Activation enthalpy : 90.8 ± 0.6 kJg−1.
Activation entropy : −126.5 ± 1.5 Jg−1K−1.
Free energy of activation: 49.9 ± 0.8 KJg−1.
The reaction rate constant and activation energy for saponification reaction, as obtained from the present work, were compared with the data reported by Mishra et al. . They reported high value of activation energy 59.71 KJg−1 as compared to the value reported in this work. Such a large variation in the values on activation energy can be attributed to errors associated with gravimetric technique by forming a precipitate of product and its drying and weighing at periodical interval, which is an offline technique.
In present work, with online conductivity measurement, it was possible to determine reaction rate constant of saponification reaction of PET waste powder and NaOH. The rapid online measurement of conductivity and use of reflux water condenser minimized the error due to CO2 pick-up from atmosphere by NaOH solution and evaporation loss of reaction product ethylene glycol during the saponification.
In view of simplicity in experimental arrangement and measurement technique, the conductivity seems to be better technique for this kinetic investigation. Early investigators found the reaction as first order by different technique [1, 2]. Our conductometric study shows the second order kinetics since both the reactants were consumed in the reaction. The reaction rate constant had also led to evaluating thermodynamic parameter for this saponification reaction. Our reported value on activation energy is lower and more precise than the value obtained by gravimetric technique reported by Mishra et al. .
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The author thanks the Director of Institute of Science, Nagpur, for providing necessary facilities to carry out this work.
- 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.
- 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.
- 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.
- 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.
- 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.
- V. N. Orekov and B. M. Rudenko, Vest Khar’kpolytech Inst., vol. 195, p. 10, 1982.
- A. Sniezko, P. Penczek, and R. Ostrysk, InstIndChemwarsaw pol., Forbe lack, vol. 87, p. 1014, 1981.
- R. D. Leaversuch, “Chemical recycling brings real versatility to solid-waste management,” Modern Plastics, vol. 68, no. 7, pp. 41–43, 1991.
- B. Mikalojezyk, A. Lubawy, M. Djewska, P. Smoczynski, and A. Pozniak, Boebel, 11, pol. Pat. PL 120, 009, 1985.
- J. W. Mandoki, VS patent 4 604 772, 1986.
- D. Paszun and T. Spychaj, “Chemical recycling of poly(ethylene terephthalate),” Industrial & Engineering Chemistry Research, vol. 36, no. 4, pp. 1373–1383, 1997.
- 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.
- 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.
- . 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.
- 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.
- Toray Industries, Japanese patent, 146 567, 1976.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- B. R. Puri, L. R. Sharma, and M. S. Pathania, Principles of Physical Chemistry, Vishal Publishing, Jalandhar, India, 2005.
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