Kinetics of delignification and hexenuronic acid decomposition during kraft pulp bleaching with peroxyacetic acid

2000 ◽  
Vol 15 (2) ◽  
pp. 142-149 ◽  
Author(s):  
Anna-Stiina Jääskeläinen ◽  
Kristiina Poppius-Levlin
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.


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

1999 ◽  
Vol 40 (1) ◽  
pp. 281-288 ◽  
Author(s):  
Işıl Akmehmet Balcıoǧlu ◽  
Ferhan Çeçen

In this study the biological treatability and TiO2 photocatalyzed oxidation characteristics of sulfate pulp bleaching effluents were investigated. The original wastes had a low biodegradability as determined by BOD5/COD ratios. Biological treatment was conducted in a batch activated sludge reactor. The non-biodegradable fraction amounted to 60% of the initial COD and compounds specific to these wastes were not removed during biotreatment. In order to enhance the biodegradability of these wastes, mixed raw effluent, C/E-H stage effluent, D/E-D stage effluent and biologically pretreated wastes were subjected to TiO2 photocatalyzed oxidation. Photocatalytic oxidation led to an increase in the BOD5/COD ratio of D/E-H stage raw and biologically treated wastewater, while chloride formation was observed in both cases in a five-hour reaction period in the presence of 1g 1−1 TiO2 and 15×10−3 M H2O2 at pH=6.5. The specific absorption values (A272nm/CODs, A254nm/CODs, A346nm/CODs, A436nm/CODs) exhibited parallel decreases during photocatalytic oxidation which indicate that oxidation reactions were nonspecific with respect to the organics present in these wastes. As a conclusion it can be suggested that biological treatment should be placed before the photocatalytic oxidation method. Even in this scheme, the application of photocatalytic oxidation could only then be favored when the COD and chloride concentrations in the wastewater were below certain values or when wastewater was diluted.


Holzforschung ◽  
2006 ◽  
Vol 60 (2) ◽  
pp. 137-142 ◽  
Author(s):  
Zhi-Hua Jiang ◽  
Jean Bouchard ◽  
Richard Berry

Abstract The finding that hexenuronic acid (HexA) groups can be selectively removed from kraft pulps by acid hydrolysis has provided an opportunity to reduce bleaching chemicals. However, there is evidence that the acid hydrolysis is not uniform. In this report, we evaluate the kinetics of acid hydrolysis of HexA in a xylan sample enriched with HexA, a conventional kraft pulp, and three modified kraft pulps: anthraquinone pulp (Kraft-AQ), polysulfide pulp (PS), and polysulfide-anthraquinone pulp (PS-AQ). We found that HexA present in the xylan and conventional kraft pulp behaved similarly toward the acid hydrolysis throughout. On the other hand, HexA present in the Kraft-AQ, PS-AQ and PS pulps was heterogeneous toward acid hydrolysis and the reaction can be separated into two pseudo-first-order kinetic phases, each of which has a different rate constant. The kinetic data provide evidence for the formation of lignin-HexA-xylan complexes during modified kraft pulping processes.


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