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Inicio Ciência & Tecnologia dos Materiais Spectral analysis of the chemical structure of carboxymethylated cellulose produ...
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Vol. 29. Núm. 2.
Páginas 55-62 (mayo - agosto 2017)
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Vol. 29. Núm. 2.
Páginas 55-62 (mayo - agosto 2017)
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Spectral analysis of the chemical structure of carboxymethylated cellulose produced by green synthesis from coir fibre
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E.U. Ikhuoriaa,
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esyikhuoria@yahoo.com

Corresponding author.
, S.O. Omorogbeb,c, O.G. Agbonlahora, N.O. Iyarea, S. Pillaib, A.I. Aigbodionc
a Department of Chemistry, University of Benin, Benin-City. 300213, Nigeria
b Materials Science and Technology Division, CSIR - National Institute for Interdisciplinary Science and Technology (NIIST), Thiruvananthapuram, Kerala - 695019, India
c Rubber Research Institute of Nigeria. Benin City. 300272, Nigeria
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Abstract

In this work, CMC was synthesized from cellulose obtained from coir fibres. The obtained CMC yield was about 64.0%. The Degree of Substitution value obtained was 0.44. The spectral pattern and thermogravimetric analysis of the synthesized CMC and cellulose were evaluated using FT-IR, XRD, and TGA/DTG. Characterization of the cellulose and CMC revealed their high crystallinity with cellulose showing a lower crystallinity value due to its lignin content. The CMC also showed a higher degree of crystallinity (56.93%) and hydrogen bonding compared to some earlier literature reports for CMC. The DTG curve revealed that the CMC had a maximum rate of degradation at about 310°C. The FT-IR spectra of the obtained CMC showed a finger print region characteristic of CMC (1590cm-1). This work shows that the spectral characteristic and crystallinity of CMC can be related to the synthetic method applied in obtaining the cellulose prior to CMC synthesis.

Keywords:
carboxymethylcellulose
spectral pattern
coir fibres
cellulose
liquid phase oxidation
degree of substitution
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References
[1]
R.J. Moon, A. Martini, J. Nairn, J. Simonsen, J. Youngblood.
Chem. Soc. Rev., 40 (2011), pp. 3941
[2]
H.A. Ambjornsson, K. Schenzel, U. Germgard.
Biores., 8 (2013), pp. 1918
[3]
R.A. Dar, I. Saba, M. Shahnawaz, M.K. Sangale, A.B. Ade, S.A. Rather, P.H. Qazi.
Adv. Enz. Res., 1 (2013), pp. 91
[4]
N. Benmouhoub, N. Simmonet, N. Agoudjil, T. Coradin.
Green Chem., 10 (2008), pp. 957
[5]
J.Z. Yi, L.M. Zhang.
J. Appl. Polym. Sci., 103 (2007), pp. 3553
[6]
R. Barbucci, A. Magnani, M. Consumi.
Macromol, 33 (2000), pp. 7475
[7]
G. Marci, G. Mele, L. Palmisano, P. Pulito, A. Sannino.
Green Chem., 8 (2006), pp. 439
[8]
L.Y. Jiang, Y.B. Li, X.J. Wang, I. Zhang, J.Q. Wen, M. Gong.
Carbohydr. Polym., 74 (2008), pp. 680
[9]
D. Pasqui, A. Rossi, F. Di Cintio, R. Barbucci.
Biomacromol, 8 (2007), pp. 3965
[10]
M. Mohkami, M. Talaeipour.
Bio. Res., 6 (2011), pp. 1988
[11]
A. Hebeish, M. Hashem, M.M.A. El-Hady, S. Sharaf.
Carbohydr. Polym., 92 (2013), pp. 407
[12]
M. Hashem, S. Sharaf, M.M.A. El-Hady, A. Habeish.
Carbohydr. Polym., 95 (2013), pp. 421
[13]
J. Wang, P. Somasundaran.
J. Coll. Interf. Sci., 291 (2005), pp. 75
[14]
W. Wang, A. Wang.
Carbohydr. Polym., 82 (2010), pp. 83
[15]
M. Pohl, G.A. Morris, S.E. Harding, T. Heinze.
Europ. Polym. J., 45 (2009), pp. 1098
[16]
J. Chen, J. Wang, X. Zhang, Y. Jin.
Mater. Chem. Phy., 108 (2008), pp. 421
[17]
B. Hoang, M.J. Ernsting, M. Murakami, E. Undzys, S. Li.
Intl. J. Pharmac., 471 (2014), pp. 224
[18]
F.G. Carmacho, E.M. Grima, A.S. Miron, V.G. Pascual, Y. Chisti.
Enzy. Microb. Tech., 29 (2001), pp. 602
[19]
W. Li, B. Sun, P. Wu.
Carbohydr. Polym., 78 (2009), pp. 454
[20]
T. Heinze, A. Koschella.
Macromol. Symp., 223 (2005), pp. 13
[21]
H.D. Heydarzadeh, G.D. Najafpour, A.A. Nazari-Moghadam.
J.W. Appl. Sci., 6 (2009), pp. 564
[22]
V. Pushpamalar, S.J. Langford, M. Ahmad, Y.Y. Lim.
Carbohydr. Polym., 64 (2006), pp. 312
[23]
T.H. Heinze, M. Schobitz, M. Pohl, F. Meister.
J. Appl. Polym. Sci. Part A. Polymer Chem, 46 (2008), pp. 3853
[24]
C. Zhang, L.M. Price, W.H. Daly.
Polym. Prep., 45 (2004), pp. 421
[25]
C. Zhang, W.H. Daly, L.M. Price.
Biomacromol, 7 (2006), pp. 139
[26]
H.D. Heydarzadeh, D.G. Najafpour, A.A. Nazari-Moghadam.
J.W. Appl. Sci., 6 (2009), pp. 564
[27]
M. Mohkami, M. Talaeipour.
BioResources., 6 (2011), pp. 1988
[28]
M. Fan, D. Dai, B. Huang.
Fourier Transform Infrared Spectroscopy for Natural Fibres, pp. 45
[29]
M. Poletto, A.J. Zattera.
S.R.M.C, J. Appl. Polym. Sci., 126 (2012), pp. 336
[30]
W. Li, B. Sun, P. Wu.
Carbohydr. Polym., 78 (2009), pp. 454
[31]
Y. Nishiyama, P. Langan, H. Chanzy.
J. Am. Chem. Soc., 124 (2002), pp. 9074
[32]
V. Stigsson, G. Kloow, U. Germgard.
Paper Asia, 10 (2001), pp. 16
[33]
K. Mae, I. Hasegawa, N. Sakai, K. Miura.
Energy Fuels, 14 (2000), pp. 1212
[34]
A. Bono, P.H. Ying, F.Y. Yan, C.L. Muei, R. Sarbatly, D. Krishnaiah.
Adv. Nat. Appl. Sci., 3 (2009), pp. 5
[35]
ASTM.
Document CK-G06 Edition, 05 (2005),
D-1439-1403
[36]
M. Elomaa, T. Asplund, P. Soininen, R. Laatikainen, S. Peltonen, S. Hyvarinen.
Carbohydr. Polym., 57 (2004), pp. 261
[37]
F. Yan Yan, D. Krishniah, M. Rajin, A. Bono.
J. Eng. Sci. Technol., 4 (2009), pp. 57
[38]
B.K. Barai, R.S. Singhal, P.R. Kulkarni.
Carbohydr. Polym., 32 (1996), pp. 229
[39]
M. Adinugraha, D. Marseno.
Carbohydr. Polym., 62 (2005), pp. 164
[40]
H. Togrul, N. Arslan.
Carbohydr. Polym., 54 (2003), pp. 73
[41]
M.L. Nelson.
R.T. O’Connor, J. Appl. Polym. Sci., 8 (1964), pp. 1325
[42]
M.-C. Popescu, C.-M. Popescu, G. Lisa, Y. Sakata.
J. Mol. Struct., 988 (2011), pp. 65
[43]
M. Poletto, H.L. Ornaghi Júnior, A.J. Zattera.
Materials, 7 (2014), pp. 6105
[44]
C.-M. Popescu, M.-C. Popescu, G. Singurel, C. Vasile, D.S. Argyropoulos, S. Willfor.
Appl. Spect., 61 (2007), pp. 1168
[45]
M. Brebu, M. Vasile.
Cellul. Chem. Technol., 44 (2010), pp. 353
[46]
M. Poletto, A.J. Zattera, M.M.C. Forte, R.M.C. Santana.
Bioresource Technol., 109 (2012), pp. 148
[47]
M. Joonobi, J. Harun.
Bioresources, 4 (2009), pp. 626
[48]
M.L. Nelson, R.T. O’Connor.
J. Appl. Polym. Sci., 8 (1964), pp. 1311
[49]
E.U. Ikhuoria, S.O. Omorogbe, O.G. Agbonlahor, R.E. Etiuma.
Am. Chem. Sci. J., 9 (2015), pp. 1
[50]
M. Poletto, A.J. Zattera.
S.R.M.C, J. Appl. Polym. Sci., 126 (2012), pp. 336
[51]
M. Wada, T. Okano, J. Sugiyama.
J. Wood Sci., 47 (2001), pp. 124
[52]
X. He, S. Wu, D. Fu, J. Ni.
J. Chem. Tech. Biotech., 84 (2009), pp. 427
[53]
J.F. Su, Z. Huang, X.Y. Yuan, X.Y. Wang.
Carbohydr. Polym., 79 (2010), pp. 145
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