Abstract

Literature is strongly contradictory about the molecular reasons for yellowing and brightness reversion of pure (lignin- and hemicellulose-free) celluloses, such as in highly bleached pulps, bacterial cellulose, or cotton linters. While oxidized groups—carbonyls (CO) and carboxyls (COOH)—have been recognized as the initiators of yellowing, they are generally always found together; thus, their effects are permanently superimposed in real-world cellulose. For this reason, their individual contributions could not be reliably determined. To tackle this conundrum, we have used a two-stage study: the employment of glucopyranose-derived model compounds and the use of special cellulosic pulps. Both substrates had either only carbonyl functions, only carboxyl functions, or defined ratios of both functionalities present at the same time. The model compounds alone already provided strong indications of the CO-related and COOH-related effects, and further confirmation was obtained by the pulp study. Here, in regard to the polymer case, the carbonyl groups are the minimum functional unit in cellulose responsible for chromophore generation (termed as the “CO effect”). The carbonyl groups are the precursors for the chromophores that are formed later upon yellowing/aging. Chromophore formation increases strictly linearly with the carbonyl content at a constant given carboxyl content. Carboxyl groups alone (i.e., in the absence of carbonyl groups) are fully innocent regarding the color generation. However, they have a strong promotive action when carbonyl groups are present (termed as the “COOH effect”), which includes acidic catalysis and an additional activation by electronic effects. The general roles of CO and COOH are the same for all aging types (e.g., thermal, acidic, or alkaline), while the respective rates of chromophore generation evidently depend on various parameters such as the temperature, medium, and pH value.Graphical abstract

Highlights

  • Yellowing and brightness reversion of celluloses, two recognizable aspects of the more general term ‘‘cellulose aging,’’ have always been linked to oxidation phenomena

  • degree of substitution (DS)-difference (DDS) plots show the difference in carbonyl/carboxyl profiles between two pulps, which is especially useful to monitor the effect of various cellulose treatments

  • The combination of model compound experiments and studies on special pulps allowed a clear definition of the factors causing yellowing of celluloses

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Summary

Introduction

Yellowing and brightness reversion of celluloses, two recognizable aspects of the more general term ‘‘cellulose aging,’’ have always been linked to oxidation phenomena. The oxidation of the only reducing chain end of cellulose (a hemiacetal) to the and irradiation), and thermal stress (high temperatures). These factors cause the yellowing individually or in combination. Considering the role of the pulp and paper industries as a mainstay in many economies worldwide, the importance of bleaching processes in the pulp and paper industries, and the customer’s notion that bright white materials are of high quality and purity, it is evident that yellowing and brightness reversion of celluloses have been a topic of great interest (Suess 2010)

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