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 groupscarbonyls (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

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Although efficient and inexpensive, conventional viscometry to determine the average degree of polymerization (DP) of cellulose may mislead the final DP because cellulose degradation occurs in the used solvents, which consist of alkaline amino complexes of transition metals, such as cupri-ethylenediamine (CED). For oxidatively damaged pulps or celluloses, viscosity-DP determinations may be more inaccurate because alkali-induced β-elimination reactions render such oxidized celluloses even more vulnerable. Despite the risk identified in many studies, a systematic investigation of the parameters affecting the viscosity-DP assessed by reliable analytics is still required. Here, a new approach evaluating the effects of CED on oxidized cellulosics was used (i.e., immediate pulp regeneration after dissolution in CED). In-depth molecular feature characterization (e.g., absolute molar masses and oxidized groups’ profiling related to molecular weight distribution) by gel permeation chromatography coupled with fluorescence and multiangle laser light scattering clarified the behavior of oxidized celluloses and the influencing parameters upon dissolution in CED.

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2,5-Dihydroxy-[1,4]-benzoquinone (DHBQ, 1) is the most prominent representative of cellulosic key chromophores, which occur almost ubiquitously in all types of aged cellulosics. The degradation of DHBQ by chlorine dioxide under conditions of industrial pulp bleaching (''D stage'') was studied, i.e. in moderately acidic medium (pH 3) at temperatures between 50 and 90°C. The degradation in the presence of excess ClO 2 generates rhodizonic acid (RhA, 5,6-dihydroxycyclohex-5-ene-1,2,3,4-tetrone, 2) as a secondary chromophore which is even more stable and more potent as a chromophore than the starting DHBQ, especially in the form of its salts. At least a threefold ClO 2 excess is needed for complete DHBQ consumption. The reaction from DHBQ to RhA involves pentahydroxybenzene (PHB, I) as an intermediate which is either readily further oxidized to RhA by excess ClO 2 or slowly reconverted to DHBQ in the absence of ClO 2. The RhA yield after 30 min reaction time had a maximum of 83% at a DHBQ/ ClO 2 molar ratio of 1:5, and decreased with increasing ClO 2 charge, reaching 38% at a DHBQ/ClO 2 ratio of

Correctness and reliability of molar mass data by viscometry in organometallic solvents (cuen, cuoxam, cadoxen) are compromised by the alkalinity of these solvents which causes immediate depolymerization especially in the case of pulps with higher carbonyl content (oxidative damage). The viscosity values thus correspond to the molar mass after the beta-elimination reactions that underly these degradative processes, which is sometimes significantly smaller than the molar mass determined by gel permeation chromatography (GPC) in the non-degrading solvent system DMAc/LiCl. Despite this well-known drawback, viscosity measurements have become a standard approach for molar mass measurements due to their ease and fastness, especially in the pulp and paper industries. A potential way to reduce the inherent error of these molar mass determinations via viscosity measurements is a reductive treatment prior to dissolution of the pulp in the organometallic solvents, which converts the labile, alkali-sensitive carbonyl structures back to the respective alcohols. Using sodium borohydride (NaBH4) on different types of cellulosic pulps, we demonstrate the beneficial effects of such a reduction step on the determined degree of polymerization (DP) for all three common solvents: cuen, cuoxam and cadoxen. Molar mass distributions and profiles of carbonyl groups were determined by GPC and by carbonyl selective fluorescence labeling (“CCOA method”). Such a reductive treatment was especially valuable for hemicellulose-containing pulps. While the decreased measurement error according to the new protocol is beyond doubt, an immediate acceptance in the pulp and paper industries is at least questionable, because the new, more correct data would not agree with the old – wrong, but consistent – numbers accumulated over years and decades. In the long run, however, the new, improved protocol will prevail here as well due to its lower error rate.