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Synthesis, Characterization, and Gas Permeation Properties

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General Introduction<br />

cellulose to decipher the impact of polar substituents on the structural characteristics<br />

<strong>and</strong> hence the gas permeation parameters of the polymeric membranes. The<br />

attenuated FFV of the polymer matrices has been described to be at the helm of the<br />

decrement in the gas diffusion <strong>and</strong> solubility <strong>and</strong> consequently the decreased gas<br />

permeability of the membranes. However, the increase in CO2 permselectivity was<br />

not so evident <strong>and</strong> has been explicated by the author to be due to the unavailability of<br />

the polar groups on the peripheries to interact with CO2. As discussed above,<br />

spherical pendants are acknowledged to endow the polymers with enhanced local<br />

mobility; therefore a blend of polar <strong>and</strong> spherical substituents was envisioned to<br />

enhance permeability without loss in CO2 permselectivity. The interpolation of<br />

moderately polar carbamoyl groups with spherical t-butyl periphery was accomplished<br />

to bring in the improved gas permeability which was much more pronounced for the<br />

carbamates of cellulose acetate while no significant decrease in CO2 permselectivity of<br />

polymer membranes has been ascribed to the retained solubility selectivity.<br />

The intricate features of synthetic strategies <strong>and</strong> mechanistic aspects of<br />

cellulosic membranes explored in the present study are anticipated to lead us to new<br />

frontiers of potential applications of this renewable energy resource.<br />

Outline of the Thesis<br />

The present dissertation delineates the synthesis of novel functional cellulose<br />

ethers/esters, their characterization <strong>and</strong> investigation of various properties, <strong>and</strong> is<br />

comprised of five chapters. A variety of functional substituents have been appended<br />

to the backbone of different organosoluble cellulosics, i.e., ethyl cellulose, cellulose<br />

acetate, <strong>and</strong> hydroxypropyl cellulose while the core synthetic strategy was to exploit<br />

the residual hydroxy protons for the sake of derivatization. The incorporated<br />

moieties encompass various silyl, perfluoroacyl, dendryl, carbamoyl, <strong>and</strong><br />

aminoalkanoyl groups, <strong>and</strong> the nature of the substituents was revealed to be of<br />

considerable significance in determining the solubility <strong>and</strong> thermal characteristics of<br />

17

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