COMPETING/PARALLEL REACTION OF CHLORINE AND CHLORINE DIOXIDE DURING KRAFT PULP BLEACHING

1993 ◽  
Vol 126 (1) ◽  
pp. 27-41 ◽  
Author(s):  
PETER W. HART ◽  
JEFFERY S. HSIEH
TAPPI Journal ◽  
2010 ◽  
Vol 9 (8) ◽  
pp. 27-35 ◽  
Author(s):  
BRIAN N. BROGDON

The present investigation meticulously analyzes how oxidative alkaline extraction can be augmented through process changes, and how these augmentations can be leveraged to optimize chlorine dioxide usage with elemental chlorine-free (ECF) sequences for a conventional softwood kraft pulp. Bleaching data from Basta and co-workers (1992 TAPPI Pulping Conference) are re-examined and re-interpreted in this study. We determined that ~60% to 65% of the overall ClO2 charge should be applied in the D0-stage. Peroxide addition to an (EOP) can replace 0.6 to 2.5 Kg. ClO2 per Kg H2O2. Boosting the (EO) temperature to 80°C is equivalent to a 70°C (EOP) with 0.25% to 0.30% H2O2,whereas a 90°C (EO) is equivalent to 0.50% – 0.75% H2O2 in a 70°C (EOP). The stoichiometric bleaching data from this study can guide decision-making for lowering chemical usage and minimize costs to reach target brightness levels with three- and five-stage sequences.


Holzforschung ◽  
2003 ◽  
Vol 57 (5) ◽  
pp. 503-512 ◽  
Author(s):  
C. S. R. Freire ◽  
A. J. D. Silvestre ◽  
C. Pascoal Neto

Summary The structural changes of E. globulus wood extractives during bleaching with chlorine dioxide (D), oxygen (O), ozone (Z) and hydrogen peroxide (P) were studied. The detailed characterisation of the extractive derivatives detected in the partially bleached D, O, P and Z pulps was achieved by performing reactions of pure reference compounds with the different bleaching agents. The results show that the unsaturated sterols and fatty acids are extensively degraded during chlorine dioxide and ozone bleaching and only partially degraded during oxygen and hydrogen peroxide bleaching. The corresponding saturated extractives as well as the long chain aliphatic alcohols and ω-hydroxyfatty acids were stable during bleaching. The main oxidation products of β-sitosterol and oleic and linoleic acids, including one chlorinated derivative of linoleic acid, were identified here for the first time in E. globulus bleached pulps and bleaching filtrates.


TAPPI Journal ◽  
2016 ◽  
Vol 15 (4) ◽  
pp. 285-295 ◽  
Author(s):  
UMIT SEZGI ◽  
JANAINA RESENDE ◽  
LEWIS SHACKFORD ◽  
JORGE COLODETTE ◽  
MARCELA ANDRADE

Mills have largely used chlorine dioxide (ClO2) for eucalyptus kraft pulp bleaching. Different mills have observed significant variation in ClO2 demand to reach full brightness (≥90 ISO). These large differences in ClO2 consumption derive from many factors. The most significant include differences in carryover loads and hexenuronic acid (HexA) contents and the level of chlorate formation across bleaching. Handling of pulp with high HexA content and ClO2 losses to chlorate can be minimized by proper operation of the ClO2 stages across the bleach plant. An oxygen delignified eucalyptus kraft pulp with a kappa of 10-12 units contains only 4-6 units actually derived from lignin. This scarce amount of lignin (0.6%-0.9%) is not able to consume high ClO2 doses and, as a consequence, the excess ClO2 applied can end up being converted into chlorate. Hence, proper optimization of ClO2 bleaching stages can save significant amounts of this oxidant. This study focused on optimizing ClO2 bleaching for a typical oxygen delignified eucalyptus kraft pulp of kappa number 11.7. Elemental chlorine free bleaching was carried out with the D0-(EP)-D1 sequence. The following conditions were varied in the D0 stage: temperature, end pH, and kappa factor. The results indicated that maximum ClO2 bleaching efficiency is achieved when minimum chlorate is formed, especially when ClO2 bleaching is adjusted in such a way that residual active chlorine is maintained to a minimum. The most significant variable affecting chlorate formation is pH; however, ClO2 doses (ClO2 concentration) also play a very important role. Chlorate formation is more intense in the D1 stage in relation to the D0 stage. Optimum conditions to run the D0 stage were 90°C, 3.5 pH, and 0.22 kappa factor.


2004 ◽  
Vol 50 (3) ◽  
pp. 242-247 ◽  
Author(s):  
Keiichi Nakamata ◽  
Youichi Motoe ◽  
Hiroshi Ohi

Chemosphere ◽  
1996 ◽  
Vol 33 (12) ◽  
pp. 2431-2440 ◽  
Author(s):  
S. Juuti ◽  
T. Vartiainen ◽  
J. Ruuskanen

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