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Nondestructive testing of defects in adhesive joints

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Abstract<br />

Swell<strong>in</strong>g behaviour <strong>of</strong> hydrogels based on crossl<strong>in</strong>ked<br />

NR/PEG block copolymers.<br />

Christ<strong>in</strong>a George and M.R. Gop<strong>in</strong>athan Nair<br />

School <strong>of</strong> Chemical Sciences, Mahatma Gandhi University, Priyadarsh<strong>in</strong>i Hills<br />

Kottayam 686560, India.<br />

E-mail: christeena.george@gmail.com<br />

A series <strong>of</strong> NR/PEG block copolymers were prepared from polyethylene glycol (PEG) and<br />

hydroxyl term<strong>in</strong>ated liquid natural rubber (HTNR) by solution polymerization and dynamics <strong>of</strong><br />

the water sorption process were studied. The effect <strong>of</strong> NCO/OH ratio and pH <strong>of</strong> the swell<strong>in</strong>g<br />

medium were <strong>in</strong>vestigated with respect to the water sorption characteristics <strong>of</strong> the hydrogels.<br />

Results <strong>in</strong>dicated that the hydrogels exhibited overshoot<strong>in</strong>g effect <strong>in</strong> their dynamic swell<strong>in</strong>g<br />

behaviour. Mechanism <strong>of</strong> sorption, sorption k<strong>in</strong>etics and transport coefficients <strong>in</strong>clud<strong>in</strong>g diffusion<br />

coefficient, sorption coefficient and permeation coefficient were also determ<strong>in</strong>ed. The sorption<br />

behaviour was found to vary with the variation <strong>in</strong> NCO/OH ratio <strong>of</strong> the block copolymers.<br />

Introduction<br />

Hydrogels are multi – component systems compris<strong>in</strong>g <strong>of</strong> hydrophilic polymeric networks capable<br />

<strong>of</strong> absorb<strong>in</strong>g enough water (> 20% <strong>of</strong> its dry weight) caus<strong>in</strong>g macroscopic changes <strong>in</strong> the sample<br />

dimension while ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g its structural <strong>in</strong>tegrity. Due to the relatively high water content <strong>of</strong><br />

these materials, they have found a plethora <strong>of</strong> applications <strong>in</strong> biomedical, pharmaceutical, food<br />

and environmental fields. Their high water content lends them high biocompatibility and makes<br />

them well tolerated when implanted <strong>in</strong> vivo. Consequently, they have emerged as promis<strong>in</strong>g<br />

candidates for a variety <strong>of</strong> biomedical applications such as drug delivery systems [1], wound<br />

dress<strong>in</strong>gs [2], contact lenses [3], artificial implants [4] etc. However, on <strong>in</strong>creas<strong>in</strong>g the water<br />

content, the mechanical strength <strong>of</strong> the hydrogel becomes lower and the gel transparency can<br />

decrease as a consequence <strong>of</strong> a macrophase separation between water and polymer. Hence to<br />

achieve a gel with high mechanical strength, transparency and water content, a composite<br />

molecular structure is needed. This structure will comprise <strong>of</strong> a hydrophilic component that<br />

absorbs large amounts <strong>of</strong> water and a hydrophobic component, which improves the mechanical<br />

strength [5]. It is accord<strong>in</strong>g to this idea that for our study we synthesized amphiphilic NR/PEG<br />

block copolymers with hydrophobic natural rubber (NR) and hydrophilic polyethylene glycol<br />

(PEG).<br />

The multitude <strong>of</strong> hydrogels available leaves numerous choices for polymeric formulations. The<br />

best approach for development <strong>of</strong> a hydrogel with desired characteristics is to correlate the<br />

macromolecular structure <strong>of</strong> the polymer with desired swell<strong>in</strong>g characteristics. The swell<strong>in</strong>g<br />

studies not only describes the amount <strong>of</strong> water conta<strong>in</strong>ed with<strong>in</strong> the hydrogel at equilibrium but<br />

also give ample <strong>in</strong>sight <strong>in</strong>to the network structure <strong>of</strong> the gels and the transport mechanisms <strong>of</strong> the<br />

water uptake process 4 . Dur<strong>in</strong>g these studies controllable volume change can be brought about <strong>in</strong><br />

the hydrogels by chang<strong>in</strong>g the surround<strong>in</strong>g conditions such as pH [6], temperature [7], salt<br />

concentrations [8], chemistry [9], electric field [10], photo irradiation [11] and solvent<br />

composition [12].<br />

Polyethylene glycol (PEG) with its desired set <strong>of</strong> properties has always been a front-runner<br />

among synthetic polymers used for design<strong>in</strong>g hydrogels primarily because <strong>of</strong> its nontoxicity and<br />

biocompatibility [4]. The dynamic swell<strong>in</strong>g behaviour <strong>of</strong> amphiphilic block copolymer based on<br />

polyethylene glycol (PEG) and polybutyl acrylate (PBA) was reported by Wang et al [13]. Bajpai

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