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A Study <strong>of</strong> mechanical properties <strong>of</strong> flax-g-poly(MA) re<strong>in</strong>forced phenol-<br />

formaldehyde composites<br />

Susheel Kalia 1* , B.S. Kaith 2 , Sanjeev Sharma 1 , and Bandna Bhardwaj 1<br />

1 Department <strong>of</strong> Chemistry, S<strong>in</strong>ghania University, Pacheri Bari, Jhunjhunu – 333 515 (Rajasthan)<br />

India<br />

2 Department <strong>of</strong> Chemistry, Dr. B.R. Ambedkar National Institute <strong>of</strong> Technology (Deemed<br />

University), Jalandhar - 144 011, Panjab, India<br />

* E-mail: susheel_kalia@yahoo.com, susheel.kalia@gmail.com<br />

Abstract<br />

In the present paper, we report the preparation <strong>of</strong> graft copolymers <strong>of</strong> flax fibers with methyl<br />

acrylate (MA) us<strong>in</strong>g Fenton’s reagent (FAS-H2O2) as redox system. Synthesized flax-g-poly(MA)<br />

was characterized with FTIR, TGA/DTA, scann<strong>in</strong>g electron microscopy (SEM), and X-ray<br />

diffraction (XRD) techniques. Composites were prepared us<strong>in</strong>g flax-g-poly(MA) as a<br />

re<strong>in</strong>forcement and phenol-formaldehyde (PF) as the b<strong>in</strong>d<strong>in</strong>g material. Mechanical properties <strong>of</strong><br />

phenol-formaldehyde composites were compared and it has been found that composites<br />

re<strong>in</strong>forced with flax-g-poly(MA) showed improvement <strong>in</strong> mechanical properties. Composites<br />

re<strong>in</strong>forced with flax-g-poly(MA) showed better tensile strength (235 N) and compressive strength<br />

(814 N) <strong>in</strong> comparison to composites re<strong>in</strong>forced with orig<strong>in</strong>al flax fiber which showed lesser<br />

tensile strength (162 N) and compressive strength (372 N). Composites re<strong>in</strong>forced with flax-gpoly(MA)<br />

shows the improved MOR, MOE, and SP.<br />

Key Words: Fiber, Flax-g-poly(MA), Composites, Mechanical Properties.<br />

Introduction<br />

The renewed <strong>in</strong>terest <strong>in</strong> the natural fiber has resulted <strong>in</strong> a large number <strong>of</strong> modifications <strong>in</strong><br />

order to br<strong>in</strong>g it at par with and even superior to synthetic fibers. A rebirth <strong>in</strong> the application <strong>of</strong><br />

natural fibers as re<strong>in</strong>forc<strong>in</strong>g agent is occurr<strong>in</strong>g ma<strong>in</strong>ly <strong>in</strong> the automobile and pack<strong>in</strong>g <strong>in</strong>dustries.<br />

Advantage <strong>of</strong> <strong>in</strong>digenous natural fiber <strong>in</strong> their applications <strong>in</strong> the preparation <strong>of</strong> composites over<br />

synthetic fibers has been reported by Paramasivam and Kalam [1]. Flax fiber is a better<br />

re<strong>in</strong>forc<strong>in</strong>g material for composites due to ecological and environmental merits and the attractive<br />

mechanical properties. Flax fiber is considered to be one <strong>of</strong> the strongest fibers among the natural<br />

fibers. Mechanical properties <strong>of</strong> polymers such as tensile strength, impact-strength, and<br />

extensibility have a direct correlation with the percentage graft<strong>in</strong>g (Pg). On graft<strong>in</strong>g crystal lattice<br />

<strong>of</strong> the polymer is disrupted but the strength <strong>of</strong> the material may act to re<strong>in</strong>force the structure [2,<br />

3]. However, if crystall<strong>in</strong>ity is not disturbed on graft<strong>in</strong>g, then cont<strong>in</strong>uous <strong>in</strong>crease <strong>in</strong> strength can<br />

be obta<strong>in</strong>ed with <strong>in</strong>crease <strong>in</strong> Pg [4]. Most <strong>of</strong> the cellulosic fibers possess both crystall<strong>in</strong>e and<br />

amorphous regions. The X-ray pattern <strong>of</strong> crystall<strong>in</strong>e polymers show both sharp features<br />

associated with regions <strong>of</strong> three-dimensional order and more diffused features characteristics <strong>of</strong><br />

molecularly disordered substances like liquid. The occurrence <strong>of</strong> both types <strong>of</strong> features <strong>in</strong> the<br />

fibers <strong>in</strong>dicates that ordered and disordered regions co-exist <strong>in</strong> crystall<strong>in</strong>e polymers. Lower<br />

crystall<strong>in</strong>ity means higher amorphous regions, which are more accessible to chemicals and water<br />

[5]. Methyl acrylate was graft copolymerized onto cellulose <strong>in</strong> alkal<strong>in</strong>e aqueous solution us<strong>in</strong>g<br />

1

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