Biobleaching of Pulp with Dioxygen in the Laccase-Mediator System. Part 1. Kinetics of Delignification

Holzforschung ◽  
2000 ◽  
Vol 54 (4) ◽  
pp. 390-396 ◽  
Author(s):  
Mikhail Balakshin ◽  
Chen-Loung Chen ◽  
Josef S. Gratzl ◽  
Adrianna G. Kirkman ◽  
Harald Jakob

SummaryKinetics of pine kraft-AQ pulp delignification with the laccase-mediator system (LMS) and the effects of variable factors on the delignification were studied. The delignification was conducted in acetate buffer solution at pH 4.5 and at 40°C under atmospheric pressure. Only a part of the residual lignin could be removed in one-stage processes. Kinetics of kappa number reduction follows a pseudo-second order rate law with pulp consistency of 10 %, mediator charge of 0.1 mmole HOBT/g pulp and laccase charage of 10 UCorioluslaccase/g pulp. Kinetics of dioxygen uptake follows a pseudo-first order rate law up to first 8 hours of the reaction and a pseudo-zero order rate law at the reaction time of 8–24 hours. The amounts of dioxygen consumed per removal of one C9-unit equivalent of residual lignin is rather high, 1.5–2.5 mole, and increases with increasing reaction time. Experimental data show that side reactions between the Laccase-Mediator System and products of oxidative degradation of lignin strongly inhibit the delignification either by chemical or physical means or both. Removal of the degraded lignin fragments by alkaline extraction effectively restores the delignification of pulp with LMS. A four-stage process consisting of consecutive treatment of pulp with dioxygen-laccase-HOBT (LMS) followed by alkaline extraction (E), (LMS-E)4, decreased kappa number of a pine kraft-AQ pulp from 21.8 to less than 5. On the basis of the kinetic data, the mechanism of the pulp delignification with LMS is discussed.

Holzforschung ◽  
2000 ◽  
Vol 54 (2) ◽  
pp. 171-175 ◽  
Author(s):  
Mikhail Yu. Balakshin ◽  
Chen-Loung Chen ◽  
Josef S. Gratzl ◽  
Adrianna G. Kirkman ◽  
Harald Jakob

Summary The kinetics of dioxygen uptake in the laccase-catalyzed oxidation of veratryl alcohol with dioxygen in the presence of ABTS, the mediator, was studied. The kinetics of dioxygen uptake consists of two phases: (1) the initial phase up to a reaction time of one hour, and (2) the second phase, after a reaction time of one hour. In the initial phase, ABTS is mainly oxidized to the corresponding cation radical. The kinetics of dioxygen uptake follows a pseudo-zero order rate law. The dioxygen uptake under the reaction condition correlates with the initial ABTS concentration according to the stoichiometric relationship of 0.25 moles dioxygen per mole ABTS. In the second phase, veratryl alcohol is mainly oxidized to veratraldehyde. The kinetics of the dioxygen uptake follows a pseudo-first order rate law. The dioxygen uptake correlates linearly with the yield of veratraldehyde. The stoichiometric ratio between the formation of veratraldehyde and the consumption of dioxygen differs slightly at different M/S ratios. On average, however, it is 0.42 moles of dioxygen per one mole of veratraldehyde formed. The reaction mechanism is discussed on the basis of the kinetic data.


Holzforschung ◽  
2001 ◽  
Vol 55 (1) ◽  
pp. 47-56 ◽  
Author(s):  
A. Potthast ◽  
T. Rosenau ◽  
K. Fischer

SummaryInvestigations into the reaction kinetics of the laccase-mediator system (LMS) have been carried out. Two widely used mediators, 2,2′-azino-bis(3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS,3) and 1-hydroxybenzotriazole (HOBT,4), were compared by means of a model reaction, the oxidation of 2,4-dimethoxybenzyl alcohol (DMBA,1) to 2,4-dimethoxybenzaldehyde (DMA,2). The consumption of dioxygen was recorded electrochemically, substrate consumption and product formation were monitored by GLC.With ABTS as the mediator, the LMS reaction proceeded in two clearly distinguishable stages. The first phase is characterized by a fast decrease in oxygen with zero-order kinetics and no detectable formation of 2,4-dimethoxybenzaldehyde (2). ABTS is converted into oxidized species, the cation radical6and the dication7, respectively. In the second phase, oxygen consumption was considerably slower and followed a second-order kinetics, while the benzaldehyde was produced according to a zero-order rate law. According to the kinetic studies, the ABTS dication, but not the enzyme itself, is acting as the actual oxidant. The rate of oxidation product formation increased with increasing mediator / benzyl alcohol ratio. Less oxygen than the equivalent amount was consumed in the second reaction stage indicating that the oxidized ABTS formed in the first stage acts as an oxidant reservoir, being reduced to ABTS in turn.The LMS reaction with HOBT (4) as the mediator did not exhibit distinguishable phases, and was characterized by a comparatively slow oxygen uptake with zero-order kinetics throughout. Enzymatic oxidation of HOBT to the HOBT radical (5), which acts as the actual oxidant towards the benzyl alcohol, was the rate-determining step. The production of 2,4-dimethoxybenzaldehyde thus followed a zeroorder rate law as well. The reaction rate increased with increasing HOBT / benzyl alcohol ratios. Increasing concentrations of4caused less oxygen to be consumed per equivalent of benzaldehyde formed, indicating the occurrence of another reaction pathway at high mediator charges. At low HOBT / benzyl alcohol ratios the HOBT radical (5) acts as one-electron oxidant and is reduced to HOBT in a reversible process. In contrast, at higher HOBT / benzyl alcohol ratios5acts as a three-electron oxidant, being irreversibly reduced to benzotriazole. At commonly employed mediator concentrations, a superposition of both mechanisms results. The pure borderline cases can only be observed at HOBT / benzyl alcohol ratios below 1 and above 6, respectively.


RSC Advances ◽  
2014 ◽  
Vol 4 (33) ◽  
pp. 17097-17104 ◽  
Author(s):  
Nora Harwardt ◽  
Natascha Stripling ◽  
Simon Roth ◽  
Haifeng Liu ◽  
Ulrich Schwaneberg ◽  
...  

Conductivity and viscosity explain part of the effect of ionic liquids on the laccase–mediator system kinetics, but not all.


1981 ◽  
Vol 36 (12) ◽  
pp. 1371-1377 ◽  
Author(s):  
M. Buback ◽  
H. Lendle

AbstractThe decomposition of tert. butylperoxypivalate dissolved in n-heptane has been measured ir-spectroscopically in optical high-pressure cells up to 2000 bar at temperatures between 65 °C and 105 °C. The reaction follows a first order rate law with an activation energy Ea = 122.3 ±3.0 kJ · mol-1 and an activation volume ⊿V≠ = 1.6 ± 1.0 cm3 mol-1 .


2011 ◽  
Vol 236-238 ◽  
pp. 1420-1424
Author(s):  
Xiao Feng Pan ◽  
Le Fan Ma ◽  
Qin Qin Qu ◽  
Jia Liang Lan ◽  
Li Hong Tan

The kinetics of reed kraft pulp oxygen delignification process is studied, suitable kinetics model determined is -dk/dt=Aexp(-E/RT) [OH-]b[PO2]cKa, and the parameters in the model is calculated. The function for estimation of the kappa number at different reaction time is established for the reed kraft pulp oxygen delignification process. The reaction order fitted is 6.72 for delignification (a), 0.87 for alkali concentration (b), and 0.62 for oxygen pressure(c), respectively. The activation energy E is 80.96KJ/mol and frequency factor A 1.5×104.


1974 ◽  
Vol 52 (15) ◽  
pp. 2667-2672 ◽  
Author(s):  
Louise Nadon ◽  
Miklos Zador

The kinetics of decomposition of the organo-thallic adduct formed in methanol between styrene and Tl(OAc)3, (C6H5—CH(OCH3)—CH2—Tl(OAc)2) has been studied in a water–methanol solvent. The reaction follows a first order rate law. The organo-thallic compound, RTl(OAc)2, is shown to be dissociated at low concentrations yielding two reactive species, RTlOH+ and RTl2+. The influence of acidity on the rate of decomposition shows that RTl2+ is much more reactive than RTiOH+. The kinetic parameters have been determined. The implication of the results on the rate-determining step of Tl(III) oxidation of styrene is discussed.


2001 ◽  
Vol 13 (1-3) ◽  
pp. 1-16 ◽  
Author(s):  
Mikhail Balakshin ◽  
Ewellyn Capanema ◽  
Chen-Loung Chen ◽  
Josef Gratzl ◽  
Adrianna Kirkman ◽  
...  

Holzforschung ◽  
2003 ◽  
Vol 57 (5) ◽  
pp. 513-519 ◽  
Author(s):  
O. García ◽  
S. Camarero ◽  
J. F. Colom ◽  
Á. T. Martínez ◽  
M. J. Martínez ◽  
...  

SummaryFlax pulp obtained by anthraquinone-soda pulping, resulting in a kappa number of 11.1, a viscosity of 950 ml/g and 36.7% ISO brightness, was bleached in a totally chlorine-free sequence using the enzyme laccase from the fungusPycnoporus cinnabarinusand 1-hydroxybenzotriazole (HBT) as redox mediator (stage L), followed by a hydrogen peroxide stage (P). The laccase treatment was optimized using a three-variable sequential statistical plan over the following ranges: 1–20 U/g o.d.p. (oven-dried pulp) laccase dose, 0.5–7.5% o.d.p. HBT dose and 1–24 h reaction time. The influence of these variables on several pulp properties after the P stage of the LP sequence was examined. The models defined from the results obtained predicted variations in ISO brightness, viscosity and kappa number of 57.6–74.8%,590–955 ml/g and 0–6.2, respectively. The variables most strongly influencing these pulp properties were found to be the reaction time and the enzyme dose. A compromise was adopted as regards the operating conditions in order to ensure optimum results. The study was completed by conducting a biobleaching assay in a pressurized reactor (590 kPa) to assess the effect of oxygen pressure. The high pressure level resulted in improved pulp properties by the laccase-mediator system.


Author(s):  
Vu Duy ◽  
Le Van Chieu ◽  
Cao The Ha

Decolorization rate of Reactive Blue 21 by peracetic acid in aqueous solutions was measured at pH 6.0. Concentrations of peracetic acid were applied in the range of 1 - 3 mM. The reaction kinetics were monitored by recording the light absorption of the Reactive Blue 21 at 660 nm. The obtained results showed that the decolorization happened via non-catalytic and auto-catalytic reactions. Both the reactions were proposed to obey the second-order rate law.


1999 ◽  
Vol 64 (11) ◽  
pp. 1770-1779 ◽  
Author(s):  
Herbert Mayr ◽  
Karl-Heinz Müller

The kinetics of the electrophilic additions of four diarylcarbenium ions (4a-4d) to tricarbonyl(η4-cyclohepta-1,3,5-triene)iron (1) have been studied photometrically. The second-order rate constants match the linear Gibbs energy relationship log k20 °C = s(E + N) and yield the nucleophilicity parameter N(1) = 3.69. It is concluded that electrophiles with E ≥ -9 will react with complex 1 at ambient temperature.


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