Investigation into the effect of a plant‐derived stabiliser on the light and wash fastness of sulphur‐dyed cotton and nylon fabrics

In this study, cotton fabric and nylon fabric were dyed with a range of commercial sulphur dyes and the light and wash fastness of the coloured fabrics was investigated. The effect of after‐treating the coloured cotton and nylon fabrics with a tannin‐based commercial product, Bayprotect Cl, in the presence or absence of sodium sulphate in the treatment bath, was found to significantly improve the light fastness of the sulphur‐dyed cotton, and the photoprotective effect was partially stable to ISO 105‐C06 washing. In addition, the tannin‐based after‐treatment also improved the colour stability of the dyed fabrics to the perborate‐based ISO 105‐C06 washing. The possible mechanisms for the improved fastness properties are also discussed. The application of sulphur dyes to nylon is potentially commercially useful but has been limited because of the reported poor light fastness of the dyeings. The photoprotective effect of the tannin‐based after‐treatment was investigated with a view to providing the necessary commercial performance. However, it was established that on this fibre, the light fastness improvement was marginal, and the associated wash fastness to oxidative bleach‐based ISO 105‐C06 washing was limited

Oxidative degradation of non-recycled and recycled paper

AbstractThe degradation of paper-based materials involves several and complex mechanisms, such as hydrolysis and oxidation. The behaviour of different types of pulps can be very variable. In this study, the difference upon oxidation of contemporary non-recycled and recycled papers, which now constitute a considerable fibre source, is investigated. A 0.015 M potassium periodate solution is used to oxidise five types of paper, two non-recycled and three recycled, for 0.5, 1, 2 and 4 h. The effects of such oxidation treatments are evaluated in terms of carbonyl content and degree of polymerisation (DP). A modified procedure of the Szabolcs's method and viscometry are used to measure the carbonyl content and DP, respectively. The carbonyl groups are found to increase more rapidly in the recycled papers than in the non-recycled ones. On the contrary, oxidation causes a larger decrease of the DP values in the non-recycled papers, the paper made of pure cellulose being the most sensitive in terms of depolymerisation. The DP values measured for pure cellulose paper are in line with previously reported data. Moreover, in accordance with the Ekenstam equation, the plots of the reciprocal of DP as a function of oxidation time show good linear correlations for all types of paper investigated. Pseudo rate constants are thus calculated from the slopes of these plots, those of the non-recycled papers being found to be higher than those of the recycled papers. Graphic abstrac

The impact of paper constituents on the efficiency of mechanical strengthening by polyaminoalkylalkoxysilanes

International audienceThe aim of the research was to evaluate the influence of certain components of paper such as lignin and papermaking additives (fillers and sizing) on the efficiency of a recently proposed treatment for simultaneous deacidification and mechanical strengthening with polyaminosiloxane copolymer networks. Mixed mechanical and chemical pulp papers containing various additives were treated with aminoalkylalkoxysilanes (AAAS) by immersion or by spray. Upon treatment, the deposited alkaline reserve varied from 0.34 to 1.14 mol kg−1. For all the papers, copolymers formed from binary mixtures of a di- and a tri-functional AAAS provided the best improvement in the mechanical properties, i.e. in the tensile strength and the folding endurance, indicating an increase in the interfiber bonding energy and in the paper flexibility and plasticity, respectively. It was found that fillers had no influence while sizing hampered the efficiency of the treatment. The presence of mechanical pulp was shown to have a significant impact on the effect of the treatments as well by increasing the tensile resistance more than the folding endurance, indicating an increase in the paper rigidity. This observation was attributed to the response of lignin to the treatment

Controlled thermo-catalytic modification of regenerated cellulosic fibres using magnesium chloride Lewis acid

The Lewis-acid catalytic reactions of magnesium chloride with regenerated cellulosic fibres under baking conditions can be interpreted using existing semi-crystalline morphological models. Reaction at 180 °C is associated with chain scission, which takes place randomly within the accessible regions of the fibre structure. This causes a rapid reduction in the cellulose degree of polymerization, which stabilizes at a limiting value, analogous to that observed with wet-state mineral acid catalysed hydrolysis. A slower scission-reaction is also observed, believed to be due to the liberation of single glucan units from crystallite ends, again analogous to wet-state mineral acid hydrolysis. Dry-state catalysis is promoted by thermal molecular motion, allowing migration of catalyst ions and also conformational flexing of the cellulose polymer, which also induces a small amount of recrystallisation at crystallite lateral surfaces. Differences in the dry-state reaction have been observed for lyocell, viscose and modal regenerated fibres, which can be related to differences in crystallinity and resulting accessibility of the magnesium chloride catalyst. For lyocell the accessibility towards magnesium chloride is lower than found with mineral acids, which may be significant in the development of treatments to promote mechanical fibrillation, without sacrificing fibre tensile properties