Demineralization Kinetics of Chitin Isolation from. Shrimp Shell Waste

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Contemporary Engineering Sciences, Vol. 1, 217, no. 29, 149-1418 HIKARI Ltd, www.m-hikari.com https://doi.org/1.12988/ces.217.79118 Demineralization Kinetics of Chitin Isolation from Shrimp Shell Waste Ahmad Fadli, Drastinawati, Komalasari, Yesi Afriani and Subkhan Maulana Department of Chemical Engineering, Faculty of Engineering, Riau University Jl. H.R Subrantas No. 12,5 Km, Pekanbaru 28293, Indonesia Feblil Huda Department of Mechanical Engineering, Faculty of Engineering, Riau University Jl. H.R Subrantas No. 12,5 Km, Pekanbaru 28293, Indonesia Copyright 217 Ahmad Fadli et al. This article is distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Chitin is a biopolymer material which widely used in any field especially for absorbent and dietary drugs. Chitin was isolated by deproteination and demineralization of shrimp shell waste. The aim of this research is determining kinetics of demineralization of chitin isolation. At first, NaOH at concentration 2,5%; shrimp shell; and HCl concentration ranges,2 1,8 N mixed at room temperature in beaker glass stirred at 5 till 2 rpm. Samples were took off the beaker glass every 5 2 minutes for 2 ml. The sample then washed until the ph was neutral. Furthermore, the chitin filtered and destructed by H2SO4 and HNO3 to determining calcium carbonate content by titration of complexometry. The results showed that the kinetic was following pseudo second order equation. The reaction rate increased along with the increasing of HCl concentration. The reaction rate in addition of HCl concentration from.2-1.8 N and stirring rate of 15 rpm increased from.3 to.44 min -. The effect of stirring rate toward reaction rate was undefined by kinetic homogenous reaction. The range of reaction rate in range.167 up to.394 min - 1. Introduction Sources of chitin are estimated to be as abundant as those for cellulose with a

141 Ahmad Fadli et al. yearly production of approximately 1 1-1 12 metric ton [11]. The shrimps production caused 6-7% of total mass become a waste that cause many environmental problems. Shrimp shell usually consist of head, skin, and tail which consists mainly of 3 4% protein, 3 5% calcium carbonate and 15-3% chitin which 8% chitin can be converted into chitosan [7]. Small portion of the waste is used for animal feed, protein hydrolyzate, silage, raw materials of shrimp paste, petis and shrimp crackers that have low selling value, but in some country has been processed into chitin and other derivates for higher selling value. Chitin and derivates are usually applied in various fields such as textile, photography, agricultures, cosmetics, biotechnology, water treatment, waste treatment, and biomedical industries [3]. Some applications require specific architectures, and the effectiveness of the polymers for these applications was shown to depend on the molecular weight distribution and the degree of deacetylation (DA) [6]. Cost-effective, fast, and easily controlled industrial process for producing chitins of high molecular weight and DA still remains to be developed [8]. According to Percot et al [8] the optimum deproteination process obtained with 1 M NaOH within 24 h at temperature close to 7 o C. The optimum demineralization also obtained within 15 min at ambient temperature in an excess of HCl.25 M (with a solid-to-liquid ratio of about 1/4 (w/v)). The results showed that content of calcium in shrimp shells is below.1% and the DA is almost 95%. Chang and Tsai [1] was reported the kinetics of chitin demineralization reaction could be review by the homogeneous reaction kinetic equation. The kinetics equation of the reaction is obtained by the quasi-order kinetics equation. The optimum results were obtained under HCl 1.7 N, and a ratio of 1: 9 ml/g with a range of k values between.2 -.17 min -1. This study was reported that chitin could be isolated from shrimp shell by deproteination and demineralization. We had successfully obtaining chitin from shrimp shell waste by using NaOH 3.5% and HCl 12 N. The effect of HCl concentration and stirring rate on the result were investigated and reported as well. 2. Experimental Deproteination has done with 3.5% NaOH solution (Merck, German) which introduced into a conical flask reacted with the powder of shrimp shell solid-toliquid ratio was 1:1 (w/v) at 65 C for 2 h and stirred using a magnetic stirrer (Dragon Lab, China) at 15 rpm of a stirring rate. The results of deproteination then quickly filtered and washed with deionized water until neutrality as determined using a ph meter. Furthermore, the precipitate dried in an oven at 1 C for 4 hours. The deproteinized shell was then soaked in.2 solution of HCl at room temperature for 1 hour with stirring rate at 5 rpm. The demineralized samples

Calcium Concentration (N) Demineralization kinetics of chitin isolation from... 1411 were dried and weighed. This was repeated in turns for other HCl concentrations.6; 1; 1.4; and 1.8 N. The entire demineralization procedure was then repeated for the stirring rate 5; 15; and 2 rpm. The concentration of calcium, in the raw as well as demineralized solid materials, was determined using complexometric titration. 3. Result and Discussion 3.1 Reactant Concentration and Stirring Rate Effects on Calcium Conversion Figure 1 shows calcium conversion at vary concentration and 25 rpm stirring rate, which the highest conversion reached 98%. The demineralization process using HCl with a concentration of.2;.6; 1; 1.4 obtained the conversion of calcium carbonates by 32%; 93%; 96%; 97%; and 98%, these results showed that the conversion of calcium carbonate increases along with the increasing of HCl concentration. The volume of HCl decreased along with time of reaction, and the conversion is inversely proportional to the addition of HCl. Also with time reaction increased, the conversion did too. Figure 1 show linearly results between conversion changed with HCl concentration. Synowiecki and Al-Khateeb [1] explained that the rate of reaction is a reduction of reagent concentration the increasing of product concentration in time union. 3 2,5 2 Figure 1. Calcium concentration at various HCl concentration 1,5 1,5,2 N,6 N 1 N 1,4 N 1,8 N 1 2 3 4 5 6 Time (minutes) Figure 1. Conversion of CaCO3 at different HCl concentration

CaCO 3 Conversion (%) 1412 Ahmad Fadli et al.,9,8,7,6,5,4,3,2,1 2 4 6 8 Time (minutes) 5 rpm 1 rpm 15 rpm 2 rpm 25 rpm Figure 2. Conversion of CaCO3 at different stirring rate The higher HCl concentration the more HCl molecular would have reacted with material such calcium carbonate molecular to produce an aqueous solution (CaCl2). Time reaction is another important factor to reduce the calcium concentration because the longer time reaction makes the more HCl molecules diffuse into chitin molecules. Another parameter we used is stirring rate which the results completely was not significant factor for demineralization due to the result obtained. Figure 2 show the conversion increasing along the stirring time, the longer stirring time was held the higher conversion percentage obtained. Based on this study the variance of stirring rate does not significantly affected the demineralization of chitin isolation. However, the stirring rate still given an influence aspect due to the conversion percentage obtained, in the first 15 minutes sampling test, at the stirring rate of 5 and 25 rpm the conversion of calcium carbonates are 94% and 96%. Non-linear results gained from the effect of stirring rate caused by CO2 gas formed from the reaction between calcium carbonate and HCl cause solids come up to the reactor walls so that stirring was uneven. So at high speed stirring the solid which powder of deproteination shrimp shell will be more attached. As explained before there were not much effect of stirring rate towards conversion. The data of the result showed in the table below. Figure 2 shows that stirring rate parameter for 5 to 25 does not have significantly differences. According to Levenspiel [4] theoretical explanation that is reaction rate just have a big impact with both of concentration-dependent term and temperature-dependent term. These experimental results showed righteousness of that theory. 3.1 Determination of Reaction Order (n) Determining of reaction order used by two methods: differential and integral method [2]. The method used in this research was integral method. The data obtained

Demineralization kinetics of chitin isolation from... 1413 from the integral method shows the order of reaction on chitin demineralization in each concentration and agitation rate were more likely to be second-order. Demineralization reaction shows as follow CaCO 3 (s) + 2HCl (l) CaCl 2(aq) + H 2O(l) + CO 2(g) (1) aa + bb cc + Dd (2) C A (M) 3 2,5 (a) 2 R² =,6981 Zero-order eq. C A = C A kt 1,5 1,5 1 2 3 4 5 6 Figure 3. Kinetic-order at,6 N HCl and 15 rpm for zero-order 2,5 2 First-order eq. ln ( C A C A ) = kt (b) ln C Ao/ C A 1,5 1 R² =,834,5 1 2 3 4 5 6 Figure 4. Kinetic-order at,6 N HCl and 15 rpm for first-order

1414 Ahmad Fadli et al. 2 1,5 1/C A 1 R² =,9191,5 Second-order eq. 1 C A = 1 C AO + kt 1 2 3 4 5 6 Time (minutes) Figure 5. Kinetic-order at,6 N HCl and 15 rpm for second-order d [A] d [B] m n r = = = kc dt dt A C B (3) If the amount of HCl used in excess volume, so it assumed that HCl concentration does not change during the process, thus the rate of demineralization reaction is only influenced by the concentration of calcium carbonate. r = dc A dt = kc A m (4) Where k` is k [HCl] n and we want to determine the n (reaction order) value. Demineralization in this study was observed at zero-order, first-order and second order kinetics. a. The zero-order (m = ) is a reaction that occurs when the magnitude of the reaction rate is not affected by the reactant concentration. The zero-order reaction equation is shown in the following equation: ( dc A ) = k (5) dt and after integrating we have C A = C A kt (6) Once integrated and applied to the graph when the process occurs at time (t) versus the magnitude of the CA concentration. Zero-order is shown in Figure 3. b. The first-order (m = 1) is a reaction which rate of reaction directly proportional to the concentration of the reactants. r = dc A dt = k C A (7)

k (1/minute) Demineralization kinetics of chitin isolation from... 1415 In C AO C A = kt (8) Once integrated and applied to the graph it was shown by Figure 4. c. The second order (m = 2) is a reaction which speed is proportional to the square of the concentration of one of its reactants or by the product of the concentration of the two reactants. For the second order reaction equation, the equation becomes as follows. r = dc A dt = k C A 2 (9) 1 = 1 + kt (1) C A C A Once integrated and applied to the graph it was shown by Figure 5. Based on the values of percentage error it was indicate small difference of the reaction rate constant (k) between theoretical and data were obtained at second-order kinetics. The highest and lowest percentage error showed respectively by second-order and zero-order with 75.48% and 1.13%. According to Levenspiel [4] the smaller percentage error means smaller deviance of graphical. It also showed second-order kinetics deviance standart were smaller and more relevant to theoretical and experimental results. 3.2 Effect of Reactant Concentration and Stirring rate on Reaction Rate Constant (k) Reactant concentration is one of the influence factors that can extremely affecting the rate of reactions. The greater concentration of reactant will cause significant conversion increase and faster reaction.,4,35,3,25,2,15,1,5,5 1 1,5 2 HCl Concentration (N) Figure 6. The relationship between HCl concentration and reaction rate constant

1416 Ahmad Fadli et al. The increasing of concentration reactant causes the reaction move to shift at the right side and will increasing the collision frequency thus increasing the rate constant of reactions. Le Chatelier principles declared there were changing inside a system that was in the equilibrium condition, it will shift equilibrium in the direction which could restore to initial state. Theoretically a substance can react with other substance if the particles collide with each other, and then the collision will produced energy to begin the reaction. According to Arrhenius formula The way to speed up the collision process is stirring [4]. Figure 6 shows the increasing of k value along the increasing of HCl concentration and stirring rate. The value of k at.2;.6; 1; 1.4; and 1.8 N at 5 rpm are.16/minute;.77/minute;.136/minute;.163/minute and.23/minute. The lowest k value just only reach.16/minute when the addition of.2 N while the highest k value reach number of.23/minute obtained when the addition 1.8 N of HCl. Figure above also shows that the effect of stirring rate on reaction rate constant. The addition of 1.8 N HCl at 5; 1; 15; 2; and 25 rpm obtained k values are.23/minute;.299/minute;.22/minute;.2/minute; and.22/minute. These fluctuating data caused by CO2 gas formed from the reaction between calcium carbonates and HCl that formed solid to come up into the reactor walls which causing the stirring was uneven. 3.3 FT-IR Analyzing FT-IR analysis aims to identify the clusters that form a compound so that the known compounds can be known. Figure below show the graphical analyzing of chitin, generally interpretation of chitin spectrum of FT-IR i.e the absorbance band 3649-32 cm -1 show the vibration of OH; NH asymmetric groups in the 3267 cm -1 ; 3125.5-2891 cm -1 shows CH-aliphatic vibration; 131 cm -1 showing CN vibration; 1654 cm -1 showing a vibration C = O and the absorption of 156 cm -1 indicating vibration of NH Amide II (Liu et al, 212). FT-IR Analyzed showed a results obtained OH group in the absorption of 344 cm -1 ; the α-ch vibration in the absorption of 2829 cm -1 and also seen uptake at 13 cm -1 as CH-buckling; and C = O vibration as the amide group at 1666 cm -1. Wavenumber (cm -1 ) Figure 7. The Result of FT-IR Analyze of Chitin Isolation

Demineralization kinetics of chitin isolation from... 1417 Based on functional group analysis showed that the chitin isolation which obtained from shrimp shell waste contained chitin-forming groups and the uptake pattern was close to chitins. 3.4 Comparison with Previous Research The related research homogenous demineralization kinetics had done by Chang (1997) with raw material type Solonecera Melantho or called red shrimp. Table 2. The Comparison this study with previous research Information Chang (1997) This Study (217) Raw Material Solonecera Melantho Metapenaeus sp. Reaction Order Pseudo first order Pseudo second order k Range.156 -.17 min -1 Range.255 -.4 min -1 Raw material Composition Protein: 18.1%, Fat:.8%, Calcium: 16.1%, Chitin : 17.4% Protein: 24.3%, Fat: 5.14%, Calcium: 16.6%, Chitin : 18.7% 4. Conclusion Based on results of this study, it was found a great effects of HCl concentration to calcium conversion. Higher conversion was obtained by added 1.8 N HCl which increase conversion up to 98%. The opposite results were showed from stirring rate as a parameter which nonlinear data obtained caused by most of physical factor. Stirring rate does not significantly affected the conversion yield, for the same time and HCl concentration. The reaction kinetics obtained follow the pseudo-second-order kinetics equation. Acknowledgements. This studied was supported by Ministry of Research, Technology and Higher Education of the Republic of Indonesia. References [1] K.L.B. Chang and G. Tsai, Response surface optimization and kinetics of isolating chitin from pink shrimp (Solenocera melantho) shell, Journal of Agriculture Food Chemistry, 45 (1997), no. 5, 19-194. https://doi.org/1.121/jf96687

1418 Ahmad Fadli et al. [2] H. S. Fogler, Elements of Chemical Reaction Engineering, 3th Ed, Prentice-Hall Incorporation, New Jersey, 1999. [3] E. Khor, Chitin: Fulfilling a Biomaterials Promise, Elsevier Ltd., United States of America, 21. [4] O. Levenspiel, Chemical Reaction Engineering, 3 rd edition, John Willey and Sons Inc, Singapore, 1999. [5] S. Liu, J. Sun, L. Yu, C. Zhang, J. Bi, F. Zhu, M. Qu, C. Jiang and Q. Yang, Extraction and characterization of chitin from the beetle Holotrichia Parallela Motschulsky, Molecules, 17 (212), 464-4611. https://doi.org/1.339/molecules174464 [6] R.A.A. Muzzarelli, Chitin, Pergamon Press, New York, 1977. [7] No, H.K. and S.P. Meyers, Preparation and Characterization of Chitin and Chitosan-A Review, Journal of Aquatic Food Product Technology, 4 (1995), no. 2, 27-52. https://doi.org/1.13/j3v4n2_3 [8] A. Percot, V. Cristophe and D. Alain, Optimization of chitin extraction from shrimp shells, Biomacromolecules, 4 (23), 12 18. https://doi.org/1.121/bm2562k [9] G.A.F. Roberts, Chitin Chemistry, 1 st ed, MacMillan, London, Springer, 1992. https://doi.org/1.17/978-1-349-11545-7 [1] E. Z. Sikorski, Chemical and Functional Properties of Food Components, 3 rd edition, CRC Press, United States of America, 27. [11] J. Synowiecki and N.A. Al-Khateeb, Production properties and some new applications of chitin and its derivatives, Critical Reviews Food Science and Nutrition, 43 (23), 145-171. https://doi.org/1.18/1486939826473 Received: October 1, 217; Published: December 15, 217