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ABSTRACT:Crystal structure and mechanical properties of cellulose fibers were studied to investigate the effect of chemical treatment on the fiber. Pretreatment by acetone extraction, mercerization with 3-20% wt/v sodium hydroxide (NaOH), and acrylonitrile (AN) grafting initiated by azo-bis-isobutylonitrile were performed. From Fourier transform infrared spectroscopy and wide-angle X-ray diffraction quantitative measurements, the pretreated fibers showed an induced slight decrease of crystallinity index. The structural transformation of the fibers from cellulose I to cellulose II was observed at high NaOH concentration of 10 -20% wt/v. The amount of grafting, 1.56, 2.94, 6.04, 8.34, or 10.46%, was dependent upon the initiator concentration and the volume of monomer in the reactor. The AN grafted fibers had no transformation of crystalline structure as observed after mercerization. Only a variation of X-ray crystallinity index with grafting amount was observed. Moisture regain of pretreated and modified fibers depended on the structure of the fiber and the amount of grafting. The mechanical properties performed by a single fiber test method were strongly influenced by the cellulose structure, lateral index of crystallinity, and fraction of grafting. Scanning electron microscopy was used for analysis of surface morphologies of treated fibers.

Bioscouring of hemp (Cannabis Sativa L) using pectate lyase (EC 4.2.2.2), Scourzyme L, was performed at 55 degrees C and pH 8.5 in a nonagitated system. The enzyme concentration, treatment time and substrate concentration were varied to obtain the kinetic constants, K(m) and V(m). Greater enzyme concentration and a longer treatment improved the removal of the low methoxy pectin component as indicated by UV spectroscopy. Removal of pectate caused no crystalline transformation in the fibres, except for a slight decline in the crystallinity order index analysed by Fourier Transform infrared spectroscopy and wide angle X-ray diffraction. This corresponded well with the single fibre bundle tensile mechanical properties test. Smooth surfaces and separated fibres observed using SEM images were evidence of successful treatment, supported by weight loss at low temperature of a pectic substance. After treatment, the pectin substance was no longer observed during thermogravimetry. An increase in surface area and pore size after scouring were further evidence of modification.

The structural degradation of cellulose fibre from hemp (Cannabis Sativa L.) by a ball-milling process and the recrystallization behavior of the product were studied. A linear increase in the Brunauer -EmmettTeller specific surface area was observed; indicating the fibre bundles were being crushed and disrupted to single fibres, which was confirmed by SEM. An increase in the milling duration gradually destroyed the crystalline structure of the cellulose fibres, observed by a reduction of the 002 plane intensity in wide angle X-ray scattering measurements. The crystalline order index calculated from the area ratio of the 002 to the 021, 101 and 002 planes was decreased from 65 to 36 after milling for 330 min. Subsequently the lower thermal stability of ball-milled fibre was observed from a decrease in the temperature at the maximum mass loss rate using thermogravimetry. An increase in solvent polarity, solvent-fibre ratio, agitation speed and drying rate resulted in the rearrangement of ball-milled cellulose crystalline structure to a greater order. Moreover, an increase in the BET specific surface area and the amorphous fraction improved the scouring efficiency of the ball-milled cellulose using the pectate lyase enzyme (EC. 4.2.2.2).

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