International Journal of Polymer Science
Volume 2015 (2015), Article ID 470928, 4 pages
http://dx.doi.org/10.1155/2015/470928

Research Article

Synthesis of Cotton from Tossa Jute Fiber and Comparison with Original Cotton

Md. Mizanur Rahman,¹ Md. Rezaur Rahman,² Sinin Hamdan,¹ Md. Faruk Hossen,² Josephine Chang Hui Lai,² and Fui Kiew Liew¹

¹Department of Mechanical and Manufacturing Engineering, Faculty of Engineering, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia
²Department of Chemical Engineering and Energy Sustainability, Faculty of Engineering, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia

Received 6 March 2015; Accepted 24 March 2015

Academic Editor: Vijay K. Thakur

Copyright © 2015 Md. Mizanur Rahman et al. This is an open access article 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.

Cotton fibers were synthesized from tossa jute and characteristics were compared with original cotton by using FTIR and TGA. The FTIR results indicated that the peak intensity of OH group from jute cotton fibers occurred at 3336 cm⁻¹ whereas the peak intensity of original cotton fibers occurred at 3338 cm⁻¹. This indicated that the synthesized cotton fiber properties were very similar to the original cotton fibers. The TGA result showed that maximum rate of mass loss, the onset of decomposition, end of decomposition, and activation energy of synthesized cotton were higher than original cotton. The activation energy of jute cotton fibers was higher than the original cotton fibers.

1. Introduction

In recent years, lignocellulosic materials have grown to be more attractive to the material engineering sectors. These materials, comprising lignin, hemicellulose, and cellulose, have become alternatives to conventional materials. This is due to their environmentally friendly nature and lignocellulosic materials are derived from plants. If the cellulose resources can be fully utilized, much energy can be saved and the environmental pollution can be decreased [1].

Jute is a natural biodegradable fiber, largely produced in India, China, and Bangladesh. In recent years, the development of biodegradable materials from renewable sources has increased [2]. Jute fibers are durable with many advantages, which include low cost, low density, and light weight. Jute fibers are conventionally used as packaging material and carpet backing. Nowadays, jute fiber of improved qualities has attracted its use in different areas, namely, technical textiles, jute gunny sack, jute gunny bag, jute yearn, household textiles, and so forth [3]. Therefore, it is important to develop new products from jute to regain its economic importance. Original cotton fiber is a natural soft fiber obtained from the boll of the cotton plant.

The largest producing areas of cotton are China, India, Pakistan, Bangladesh, Republic of Uzbekistan, Brazil, Australia, Greece, and Syria. Original cotton is stable with many advantages such as low cost, light weight, and easy possessing. The original cotton fibers are conventionally used in medical sector and household textiles. Presently, original cotton fibers are increasingly used in different items, like paper, fiber pulp, food casing, textile mills, spinning mills, knitting mills, and so forth. The original cotton production, however, is less than the actual demand. Therefore, synthesized cotton fibers can be used to fulfill the high demand for original cotton.

Acetic acid and alkali processing is an effective alternative method to fabricate jute cotton fibers [4]. This method also includes dewaxing and delignification. The fabricated cotton fibers derived from jute fibers possess improved properties [5]. The synthesized jute cotton fibers can be used for diverse purposes. In this present work, a new technique and chemical process were developed to prepare cotton from jute fibers, and the result was compared with the characteristics of original cotton fiber.

2. Materials and Methods

2.1. Materials

Chemicals used in this study were ethanol approximately 96% (C₂H₆O), hydrogen peroxide 35% (H₂O₂), supplied by Brightchem Sdn Bhd. Malaysia, toluene (C₆H₅CH₃), acetic acid (glacial) 100% (CH₃COOH), titanium (IV) oxide (TiO₂), and potassium hydroxide (solid KOH), supplied by Mallinckrodt Baker, Inc., Sweden. The jute fibers were collected from Bangladesh Jute Research Institute (BJRI), Dhaka, Bangladesh.

2.1.1. Fiber Extraction

The raw jute fibers were cleaned and then washed with tap water to remove dust and other undesirable elements. After that, the jute fibers were air-dried for two days under direct sunlight. The middle parts of the jute fibers were taken and chopped into lengths of approximately 3 mm. Then, the chop fibers were placed in a forced air convection oven for drying to remove the moisture content, with a temperature of 105°C for 24 hours to ensure that all the moisture has evaporated.

2.1.2. Dewaxing

The dewaxing was done by applying the Leavitt-Danzer method. In this process, two types of chemicals were used, namely, toluene (C₆H₅CH₃) and ethanol (C₂H₆O), with ratios of 2 : 1. The extraction process was done using the extraction column (Soxhlet extractor, Round Bottom Flask, Liebig Condenser, Heater, Membrane, and Thermometer). Then, the chopped jute fibers were immersed in the extraction column. This process was continued for 3 hours at 150°C. The collected fibers were later placed in the forced air convention oven for 24 hours at 75°C.

2.1.3. Delignification

The delignification was implied using acetic acid (CH₃COOH) and hydrogen peroxide (H₂O₂) in present titanium oxide (TiO₂) in a round bottom vector vessel. Then, the dewaxed jute fibers were placed in the round bottom vessel. This process was continued for 3 hours at 130°C. After this, the collected fibers were carefully washed and placed in the forced air convention oven for 24 hours at 70°C.

2.1.4. Alkali Treatment

Potassium hydroxide (6%) (KOH) was placed in 1000 mL of conical flax and the delignified jute fibers were immersed in the solution for eight hours at 30°C and 60°C, respectively. After that, the collected samples were carefully washed and placed in the forced air convention oven for 24 hours at 70°C. Dried fibers used as synthesis cotton fibers characterization are shown in Figure 1.

Figure 1: Flow chart of the synthesized jute cotton fibers.

2.2. Microstructural Analysis

2.2.1. Fourier Transform Infrared (FTIR) Spectroscopy

The infrared spectra of the synthesized cotton fibers from jute and original cotton fibers were recorded on a Shimadzu FTIR Spectrophotometer with dynamic alignment system sealed interferometer with autodryer and wavenumber range was 350 to 7,800 cm⁻¹. The obtained spectra are presented and discussed in Section 3.

2.2.2. Thermogravimetric Analysis (TGA)

Thermogravimetric analysis (TGA) was used to study the thermal stability of synthesized cotton fibers from jute fibers and original cotton fibers. The thermal stability analysis was performed using Perkin-Elmer thermal analyzer (TGA). The specimen (10 mg) was heated from room temperature to 800°C at a dynamic heating rate of 5°C/min under N₂ using a flow rate of 100 mL/min.

3. Result and Discussion

3.1. Fourier Transform Infrared (FTIR) Spectroscopy

The FTIR spectroscopic analyses of the cotton fibers from jute and original cotton fibers are shown in Figure 2. The wavenumber from 3600 to 3000 cm⁻¹ corresponded to the stretching of H bonds in the OH groups [6, 7]. The IR spectrum showed the peak intensity of jute cotton fibers at 3336 cm⁻¹ of OH groups whereas the original cotton fibers peak intensity was recorded at 3338 cm⁻¹.

Figure 2: FTIR spectra of (a) jute cotton fiber and (b) original cotton fiber.

Stretching of the C-H group of synthesized jute cotton fibers occurred at 2897 cm⁻¹ while the original cotton fibers showed stretching at 2890 to 2362 cm⁻¹ [8]. The C=O absorption band for jute cotton occurred at 1654 cm⁻¹ and the original cotton fibers absorption band occurred at 1648 cm⁻¹ [9]. The absorption band of synthesized jute cotton and original cotton fibers at 1313 and 1321 cm⁻¹ can be attributed to the symmetrical deformation of NO₂ in the cellulose azo compound [10]. Therefore, the FTIR results proved that both synthesized jute cotton fibers and original cotton fibers possess similar properties.

3.2. Thermogravimetric Analysis (TGA)

Thermogravimetric analysis (TGA) was carried out on the synthesized cotton fibers and original cotton fibers to determine the thermal stability. The thermal stability of synthesized cotton fibers and original cotton fibers is shown in Figure 3. The weight losses of synthesized cotton fibers and original cotton fibers can be illustrated in three stages: (1) dehydration of absorbed moisture and water (<200°C), (2) the breaking of the cellulose chain of C-C and C=O (200~380°C), and finally (3) aromatization (>380°C), the residual chair formation [11].

Figure 3: TGA curves of jute cotton fibers and original cotton fibers.

From the thermogravimetric analysis on synthesized cotton fibers, it is anticipated that dehydration is approximately 4.6% of water. According to Rahman et al. [12] there is no degradation up to 160°C. Above this temperature, the thermal property decreases gradually and decomposition occurs. The initial and final temperature decompositions (, ) of jute cotton fibers were slightly higher than that of original cotton fibers which is shown in Table 1. The larger activation energy showed higher stability. The activation energy of jute cotton fibers was slightly higher than the original cotton fibers. Therefore, it can be assumed that the synthesized jute cotton fibers and original cotton fibers possess similar properties regarding thermal stability.

Table 1: Thermal characteristics of jute cotton fibers and original cotton fibers.

Sample names

Activation energy,

(°C)a
(°C)b
(°C)c
(%)d
(%)e
(%)f
(J/°K)

Jute cotton fibers
200
301
673
88.44
82.87
43.58
59.09

Original cotton fibers
39
296
492
81.32
71.74
35.10
52.25

aTemperature corresponding to the beginning of decomposition.

bTemperature corresponding to the maximum rate of mass loss.

cTemperature corresponding to the end of decomposition.

dMass loss of temperature corresponding to the beginning of decomposition.

eMass loss of temperature corresponding to the maximum rate of mass loss.

fMass loss of temperature corresponding to the end of decomposition.

4. Conclusions

In this study, jute cotton fibers were synthesized by chemical processes. The FTIR spectrum showed that synthesized jute cotton fibers characteristic band was very similar to the original cotton fibers. The TGA result also showed that the maximum rate of mass loss, onset of decomposition, end of decomposition, and activation energy for synthesis jute cotton fibers were slightly higher than original cotton fibers. It can be concluded that synthesized cotton fiber characteristics were similar to the original ones.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors would like to acknowledge the Ministry of Higher Education of Malaysia and Universiti Malaysia Sarawak for their financial support, Grant no. ERGS/02 (08)/860/2912 (12).

References

Y. D. Wu, J. M. He, Y. D. Huang, F. W. Wang, and F. Tang, “Oxidation of regenerated cellulose with nitrogen dioxide/carbon tetrachloride,” Fibers and Polymers, vol. 13, no. 5, pp. 576–581, 2012.

B. M. Cherian, A. L. Leão, S. F. De Souza et al., “Cellulose nanocomposites with nanofibres isolated from pineapple leaf fibers for medical applications,” Carbohydrate Polymers, vol. 86, no. 4, pp. 1790–1798, 2011.

S. Sengupta and S. Debnath, “Studies on jute based ternary blended yarns,” Indian Journal of Fibre and Textile Research, vol. 37, no. 3, pp. 217–223, 2012.

M. S. Jahan, A. Saeed, Z. He, and Y. Ni, “Jute as raw material for the preparation of microcrystalline cellulose,” Cellulose, vol. 18, no. 2, pp. 451–459, 2011.

H. Takagi and A. Asano, “Effects of processing conditions on flexural properties of cellulose nanofiber reinforced ‘green’ composites,” Composites Part A, vol. 39, no. 4, pp. 685–689, 2008.

L. Wang, G. Han, and Y. Zhang, “Comparative study of composition, structure and properties of Apocynum venetum fibers under different pretreatments,” Carbohydrate Polymers, vol. 69, no. 2, pp. 391–397, 2007.

Y. Sun, L. Lin, H. Deng et al., “Structural changes of bamboo cellulose in formic acid,” BioResources, vol. 3, no. 2, pp. 297–315, 2008.

Y. Bulut and A. Aksit, “A comparative study on chemical treatment of jute fiber: potassium dichromate, potassium permanganate and sodium perborate trihydrate,” Cellulose, vol. 20, no. 6, pp. 3155–3164, 2013.

E. Sinha and S. K. Rout, “Influence of fibre-surface treatment on structural, thermal and mechanical properties of jute fibre and its composite,” Bulletin of Materials Science, vol. 32, no. 1, pp. 65–76, 2009.

M. S. Islam, S. Hamdan, M. R. Rahman, I. Jusoh, A. S. Ahmed, and M. Idrus, “Dynamic young's modulus, morphological, and thermal stability of 5 tropical light hardwoods modified by benzene diazonium salt treatment,” BioResources, vol. 6, no. 1, pp. 737–750, 2011.

H. Wang, L. Huang, and Y. Lu, “Preparation and characterization of micro- and nano-fibrils from jute,” Fibers and Polymers, vol. 10, no. 4, pp. 442–445, 2009.

M. R. Rahman, S. Hamdan, A. S. Ahmed et al., “Thermogravimetric analysis and dynamic Young's modulus measurement of N,N-dimethylacetamide-impregnated wood polymer composites,” Journal of Vinyl and Additive Technology, vol. 17, no. 3, pp. 177–183, 2011.