SummaryAlmost all matter including viscoelastic cellulose respond to energy changes which almost invariably influence its atomic and molecular bond characteristics (length, orientation, and geometry). Changes in bond characteristics and quantised energy states/levels of conformationally isomeric cellulose is characterised by variations in the relative amounts of rotamers which has implications on the molecular organization and physical properties/integrity of cellulose that informs the processing and material application of cellulose. Cellulose is also reported to be auxetic. To fully establish how variations in the relative amounts of rotamers impact molecular organization and physical properties/integrity of cellulose and auxetics typical of crystalline cellulose as is usually found in non-native sources, a 1D bundle of cellulose microfibrils and 2D networks of cellulose mircofibrils were stretched in a Deben microtester, and their molecular straining followed with Raman spectroscopy. In generality, the amounts of rotamers was found to decrease with stress or strain, which influences the level of molecular order or disorder (degree of crystallinity), and in turn changes (inter-conversions) of cellulose conformations/allomorphs or even polymorphs. The auxetics of crystalline cellulose was also found to be around unity (-1.00).
Expanded backgroundAlmost all matter respond to quantised energy changes as occurs in chemical reactions or physical loading, which almost invariably influence atomic and molecular organisation, bond characteristics (orientation and geometry) which in turn results in changes in energy states of matter. This change in atomic and or molecular bond characteristics is even more dramatic and crucial in in viscoelastic polymers (polymers with side chains). Cellulose as a plentiful, renewable, tuneable, affordable, non-toxic, semi-crystalline, lightweight, thermally stable, stiff and green viscoelastic polymer, exhibits conformational isomerism under quantised energy change (be it endothermic or exothermic) in which its isomers (low energy side chains) are found to solely rotate about at least one characteristic sigma bond as occurs in the CH2 (C-6) scissor mode of -CH2OH (hydroxymethyl/methylene bridge) functional group/moiety on (C-6) of cellulose (Jarvis; Agarwal and Ralph). Three kinds of rotamers, namely: gg (gauche-gauche), gt (trans-gauche) and tg (gauche-trans) characterize this scissor mode, and according to Argawal and Ralph (2014), the relative amounts of these three rotamers, are found to influence the intensity, shape and frequency of spectra located at 1460 cm -1 , 1470 cm -1 and 1480 cm -1 Raman bands corresponding to each kind of rotamer respectively. The relative amounts of the three ratamers varies within and between native (unprocessed) cellulose I and non-native (processed) cellulose I (i.e cellulose I, II, III, IV), with relative amounts of rotamers being significantly higher and more complex in native cellulose than non-native cellulose (Argawal and Ralph, 2014). Neverthele...