A novel population balance model for the dilute acid hydrolysis of hemicellulose
- Ava A Greenwood^{1}Email author,
- Troy W Farrell^{1},
- Zhanying Zhang^{2} and
- Ian M O’Hara^{2}
https://doi.org/10.1186/s13068-015-0211-5
© Greenwood et al.; licensee BioMed Central. 2015
Received: 18 September 2014
Accepted: 23 January 2015
Published: 19 February 2015
Abstract
Background
Acid hydrolysis is a popular pretreatment for removing hemicellulose from lignocelluloses in order to produce a digestible substrate for enzymatic saccharification. In this work, a novel model for the dilute acid hydrolysis of hemicellulose within sugarcane bagasse is presented and calibrated against experimental oligomer profiles. The efficacy of mathematical models as hydrolysis yield predictors and as vehicles for investigating the mechanisms of acid hydrolysis is also examined.
Results
Experimental xylose, oligomer (degree of polymerisation 2 to 6) and furfural yield profiles were obtained for bagasse under dilute acid hydrolysis conditions at temperatures ranging from 110°C to 170°C. Population balance kinetics, diffusion and porosity evolution were incorporated into a mathematical model of the acid hydrolysis of sugarcane bagasse. This model was able to produce a good fit to experimental xylose yield data with only three unknown kinetic parameters k _{ a },k _{ b } and k _{ d }. However, fitting this same model to an expanded data set of oligomeric and furfural yield profiles did not successfully reproduce the experimental results. It was found that a “hard-to-hydrolyse” parameter, α, was required in the model to ensure reproducibility of the experimental oligomer profiles at 110°C, 125°C and 140°C. The parameters obtained through the fitting exercises at lower temperatures were able to be used to predict the oligomer profiles at 155°C and 170°C with promising results.
Conclusions
The interpretation of kinetic parameters obtained by fitting a model to only a single set of data may be ambiguous. Although these parameters may correctly reproduce the data, they may not be indicative of the actual rate parameters, unless some care has been taken to ensure that the model describes the true mechanisms of acid hydrolysis. It is possible to challenge the robustness of the model by expanding the experimental data set and hence limiting the parameter space for the fitting parameters. The novel combination of “hard-to-hydrolyse” and population balance dynamics in the model presented here appears to stand up to such rigorous fitting constraints.
Keywords
Background
Sugarcane bagasse is a promising feedstock for the production of second-generation bioethanol, whereby the cellulosic material within bagasse is hydrolysed by enzymes to produce glucose, which is subsequently fermented to produce bioethanol [1,2]. Bagasse fibres are structurally complex, comprised of three key materials: cellulose, hemicellulose and lignin. Hemicellulose forms a monolayer coating around cellulose and thus inhibits the enzymatic saccharification process [3,4]. Acid pretreatment is a method of removing hemicellulose from bagasse by hydrolysing the linkages between the monomeric units of the hemicellulose polymers. This allows enzymes greater access to the cellulosic material. Ensuring the efficiency of acid pretreatment improves the overall cost-effectiveness of bioethanol production from second-generation feedstocks [5].
Mathematical models can prove to be useful in testing the impact of varying reaction conditions upon a chemical system, with a significant time and cost saving compared to experimentation. Models may also help to inform the influence that certain input parameters and experimental conditions have upon the reaction outcomes. However, the ability of a model to both represent the chemical and physical behaviours of a system and to predict experimental outcomes must be carefully scrutinised. Without testing the robustness of a model, there may be little confidence attached to its outcomes.
A simple model of acid hydrolysis is the Saeman kinetic model in which hemicellulose is hydrolysed to form xylose, which in turn produces its own degradation products [6]. A particularly enduring variation of this model was derived by Kobayashi and Sakai in which the bagasse is portioned into two subsets, one fast hydrolysing and the other slow to hydrolyse [7,8]. Hereafter, this model is referred to as the “hard-to-hydrolyse” model. Often an oligomeric phase is introduced into these models, or a full oligomeric spectrum may be obtained through the population balance framework of Simha [9]. Such models allow for the inclusion of chain-dependent phenomena in the model, such as solubility and diffusivity. The authors have previously incorporated diffusivity and time-dependent porosity calculations into a population balance model of microscale acid hydrolysis [10]. This model was used to propose constraints on model fitting parameters but was not predictive due to the small size scale, which limited the scope for experimental validation.
In this work, we propose a fibre scale model that marries the chain length dependency of population balance equations with “hard-to-hydrolyse” kinetics. This new model also accounts for the diffusion of species from within the fibre into the surrounding hydrolysate and allows for the porosity of the material to vary temporally and spatially. The model parameters were determined by simultaneously fitting the model to experimentally obtained xylose and oligomer yield profiles (degree of polymerization (DP) 2 to 6) as well as the yield of furfural, a degradation product of xylose. By comparing the model results to oligomer profiles in addition to the monomer (xylose) yield curve, the variability associated with the model parameters is restricted. Hence, it is hypothesised that the resultant parameters carry more weight than those which have not been subjected to an equivalently stringent fitting process.
Model development
A discrete population balance approach is used to account for the chain degradation kinetics by formulating chain scission as a series of polymer degradation equations [9]. This methodology enables hemicellulose chains of all lengths to be explicitly counted, which allows for the inclusion of chain-length dependent solubility and diffusion [10]. Time-dependent polydispersity information was also collected due to the population balance equations, which provided a more stringent set of criteria to be used when parameter fitting the rate constants.
In the literature, the existence of a fast and slow hydrolysing hemicellulose fraction is readily observed [7]; however, the population balance framework does not readily allow for Kobayashi and Sakai’s separate “hard-to-hydrolyse” and “easy-to-hydrolyse” classes to be incorporated into the model [8]. In order to best approximate this phenomenon while maintaining full chain length dependence, it is assumed that the rate of hydrolysis of the slow component of hemicellulose is effectively zero on the timescale of the fast hydrolysis reaction. Consequently, there exists an unreactive portion of bagasse, (α(T)), and a hydrolysable portion, (1−α(T)), as an alternative to the easy and hard-to-hydrolyse kinetic model, where T represents temperature (K). A similar parameter has been used in conjunction with the Saeman kinetic model by Bustos et al. [11], and Zhao et al. have developed a parameter to represent the “potential hydrolysis degree” which is alike in interpretation to (1−α) [12]. Yan et al. also use a similar ratio to describe an unreactive component of cellulose in a model of cellulosic acid hydrolysis; however, the interpretation of this parameter is not the same in this context [13].
where Equations 1 through 4 describe the time (t) rate of change of the volume averaged concentrations of furfural, ϕ _{ F } (kg m ^{−3}), xylose, ϕ _{1} (kg m ^{−3}), aqueous oligomers, ϕ _{ i } i=2,…,m (kg m ^{−3}) and reactive xylan, ϕ _{ i } i=m+1,…,N (kg m ^{−3}), respectively. Here, \(\phantom {\dot {i}\!}\psi _{H^{+}}\) (mol m ^{−3}) is the effective acid concentration given by \(\epsilon _{v} C_{H^{+}}\phantom {\dot {i}\!}\). It is assumed that only one mole of hydrogen ions is liberated from one mole of sulfuric acid [14,15]. The reaction rate constants k _{ a }, k _{ b } and k _{ d } are demonstrated in Figure 2. The parameter Ω _{ i,j−i } is the breakage kernel (from the population balance kinetics), and D _{eff}(ε _{ v }) (m ^{2} s ^{−1}) represents an effective diffusion coefficient used to account for the tortuous nature of the bagasse fibre interior. Xylan was taken to have a maximum chain length of N=100. Although this falls within the range of the expected degree of polymerisation of hemicellulose (DP 80-200), the exact choice of N=100 was motivated by convenience [3].
where \({\epsilon _{v}^{3}}\) accounts for the tortuous nature of the fibre [16,17], k _{ B } (m^{2} kg s^{−2} K^{−1}) is Boltzmann’s constant, η (kg m ^{−1} s ^{−1}) is the dynamic viscosity of the acid solution and \(R_{h}(i) = 0.676l\sqrt {i} \) (m) is the hydrodynamic radius of polymer chains of length i in solution. A detailed description of the derivation of the model and these auxillary equations can be found in [10].
Equation 5 describes the porosity of the fibre as it evolves over time. It was assumed that the porosity of the fibre was initially 25.4 % (v/v) based on the porosity measurement of rice hulls [18]. Although the porosity of sugarcane bagasse has been reported in the literature, a measure of porosity as a volume fraction is specifically required for this model due to the volume averaged nature of the equations [19,20]. Sugarcane bagasse and rice hulls are both lignocellulosic agricultural residues, and hence, it is assumed that the porosity of rice hulls provides a reasonable substitute. It is difficult to validate or reject this assumption based on the SEM image of bagasse in Figure 1, since the orientation of the image and cell type featured may distort the apparent porosity [21]. The parameters \(\hat {F}\) and ε _{ α } represent the fixed volume fractions of lignocellulose and unreactive hemicellulose, respectively. The unreactive portion of hemicellulose is defined such that if the initial total volume fraction of hemicellulose is \({\epsilon _{N}^{0}}\) (assuming an initially monodisperse state, for simplicity), then \(\epsilon _{\alpha } = \alpha (T){\epsilon _{N}^{0}}\). The initial volume fractions of lignin, cellulose and xylan make up the remaining non-porous 74.6 % of the bagasse material. The initial volume fractions of cellulose, lignin and xylan were determined so as to preserve the ratio of components determined experimentally. Although these experiments measured the mass fraction of each component, the composition values were assumed to be a suitable substitute for volume fractions since the densities of lignin and hemicellulose cannot be determined.
The hydrolysate model is stated similarly to the fibre model with two notable exceptions. Firstly, as indicated in Figure 2, all insoluble chains of length i=m+1,…,N are omitted. Secondly, the void volume fraction is equivalent to the total volume of the region, ε _{ v }=1, and hence is not explicitly stated in the equations.
In this work, we take the radial distance of the hydrolysate, R _{ o }−R _{ i } to be 2.32 times that of the fibre length, R _{ i }. This was determined experimentally, whereby the volume of the hydrolysate pumped into the reactor was on average ten times the total volume of the bagasse fibres.
Parameter values used for model simulation
Parameter | Value | Units | Ref |
---|---|---|---|
\(C_{H^{+}}\phantom {\dot {i}\!}\) | 51 | mol m^{−3} | - |
0.5 | wt % | ||
R | 8.314 | J K ^{−1} mol ^{−1} | [26] |
R _{ i } | 3.75×10^{−4} | m | - |
\(D^{F}_{\infty }\) | 1.12×10^{−9} | m ^{2} s ^{−1} | [27] |
\(\hat {F}\) | 0.581 | - | - |
N | 100 | - | [3] |
m | 15 | - | [28] |
k _{ B } | 1.38×10^{−23} | m^{2} kg s^{−2} K^{−1} | [26] |
l | 0.65×10^{−9} | m | [29] |
\({\epsilon _{N}^{0}}\) | 0.165 | - | - |
where \(\hat {R}_{i}\) and \(\hat {R}_{o}\) represent the number of spatial nodes in the fibre and total domain, respectively. Water was assumed to be in excess and was not modelled explicitly. Consequently, in the model, the mass of a xylose monomer does not increase by the weight of a water molecule when scised. In reality, the yield of xylose as a mass fraction could be greater than 100% due to the addition of the water, and hence, the experimental yield must be corrected as described in the Methods section. The efficacy of this model was determined by fitting the model yields, Y _{ i }, to the experimentally obtained oligomer profiles.
Results and discussion
Dilute acid pretreatments were conducted with 0.5% H_{2}SO_{4} at five different temperatures ranging between 110°C and 170°C. For each temperature, a time series of yields was obtained for furfural, xylose and oligomers from xylobiose to xylohexaose (X _{2} – X _{6}). The maximum xylose yields obtained for each temperature ranged from 63.2 % at 110°C after 360 min to 92.1 % obtained at 155°C after 20 min. The maximum oligomer and furfural yields recorded were significantly smaller than those obtained for xylose, although some appreciable amounts of the shorter oligomer chains were recorded.
These experimental results were used to first calibrate and then validate the model presented in the Model Development section. The calibration was necessary in order to identify suitable values for the unknown model parameters by fitting the model to the experimental data collected at 110°C, 125°C and 140°C, respectively. The hemicellulose yields recorded at 155°C and 170°C were not used to fit rate parameters and hence do not appear in the Arrhenius plot discussed below. This is because the experimental yields measured at 155°C and 170°C were compromised by the automated heating time of the Dionex™ ASE™ 350. The heat up time of the solvent extractor was long compared to the timescale of acid hydrolysis at these higher temperatures; hence, the yields measured at zero static time (that is, at t=0) were non-zero to a statistically significant degree. Calculations exist in the literature to distinguish the yield due to the preheating time from the true experimental yield; however, these calculations are typically based on simpler kinetics [30]. An investigation into such calculations for non-linear population balance kinetics may provide an interesting future course of enquiry.
The calibration was completed using PEST, a model-independent parameter estimation tool. PEST uses the Gauss-Marquardt-Levenberg method to find values of the fitting parameters that minimise the discrepancies between the model results and the experimental data via least squares [31]. The sum of the squared residuals, Φ, was used to compare the accuracy of the fitting results below. The fitting parameters obtained from this calibration exercise were used to calculate parameters for 155°C and 170°C without fitting.
In this model, there exist three unknown rate parameters k _{ a }, k _{ b } and k _{ d } (m ^{3} mol ^{−1} s ^{−1}) and one unknown material parameter α. If α=0 then there is no unreactive bagasse, and the standard population balance equation system with no “hard-to-hydrolyse” consideration is resumed. It is noted that there is also some potential uncertainty in the diffusion coefficients which shall be investigated further below. Presently, however, existing formulae and information from the literature are used to estimate the diffusion coefficients in the model.
An important benefit of using population balances in the form of polymer degradation equations is that oligomer yields can be predicted for any chain length. The stringency of the fit is limited by the number of experimentally measurable oligomers in solution, rather than the model itself. Here, an analysis of the ability of the model to compare oligomer yield profiles for chains of length one to six, in addition to the yield of furfural over a range of temperatures, namely 110°C, 125°C and 140°C, is presented. The solid curves in Figure 3 demonstrate the results of using PEST to obtain the best fit between the model and the experimental yields of xylose, oligomers and furfural at 110°C. In fitting the data, k _{ a }, k _{ b } and k _{ d } are varied and α is set to zero. This approach is therefore the same as that used to fit the model to the xylose yield data without oligomers (dashed curve). However, unlike the model fit to xylose alone, the best fit of the model when all oligomer profiles are used in the fitting criteria does not correlate well (Φ=1,182) with any of the experimental profiles. This discrepancy is clear in Figure 3. Therefore, even though the model looked capable of reproducing the xylose curve, it can be seen that under a more stringent fitting regime, the model does not accurately capture the chemical and/or physical processes that are occurring during dilute acid hydrolysis of bagasse fibre, and hence, its usefulness as a predictive tool would seem to be questionable.
The validity of α as a useful fitting tool has been demonstrated; however it is important to determine the value of α as a descriptor of the mechanisms of acid hydrolysis. There are two possibilities to consider: firstly, that the introduction of an additional unknown parameter improved the fit simply by increasing the degrees of freedom in the parameter space, or alternatively that α improves the fit because it broadly captures some behaviour in the bagasse acid hydrolysis process that is influential to the yield results. To make this distinction, the model was fit with α kept fixed (α=0), but with the bulk diffusivities, D _{ ∞ } and \(D_{\infty }^{F}\) introduced as additional free parameters, thus increasing the number of free parameters in the model to five. When PEST was used to obtain the best fit between the model and experimental yield data at 110°C where k _{ a }, k _{ b }, k _{ d }, D _{ ∞ } and \(D_{\infty }^{F}\) were allowed to vary, the resultant sum of the squared residuals was Φ=1282, similar to that obtained for the case where only three parameters k _{ a }, k _{ b } and k _{ d } were fit. Interestingly, it is observed that this permutation of the model is not able to reproduce the experimental results with the same consistency as the “hard-to-hydrolyse” model, Figure 4, despite having an increased degree of freedom in the parameter space. Consequently, these results anecdotally suggest that α or some equivalent parameter that characterises the structural properties of hemicellulose in bagasse may be needed when modelling dilute acid pretreatment.
Rate parameters
k _{ a } (m ^{ 3 } mol ^{ −1 } s ^{ −1 } ) | k _{ b } (m ^{ 3 } mol ^{ −1 } s ^{ −1 } ) | k _{ d } (m ^{ 3 } mol ^{ −1 } s ^{ −1 } ) | α | |
---|---|---|---|---|
110°C | 2.0630 ×10^{−4} | 1.5434 ×10^{−5} | 7.9618 ×10^{−9} | 0.32016 |
125°C | 5.7028 ×10^{−4} | 5.7128 ×10^{−5} | 5.3401 ×10^{−8} | 0.17809 |
140°C | 1.6667 ×10^{−2} | 1.2914 ×10^{−4} | 2.6999 ×10^{−7} | 0.05211 |
k ^{0} (m ^{3} mol ^{−1} s ^{−1}) | 1.6467 ×10^{22} | 8.9850 ×10^{7} | 9.9506 ×10^{12} | - |
E _{ a } (J mol ^{−1}) | 1.9129 ×10^{5} | 9.3422 ×10^{4} | 1.54675 ×10^{5} | - |
An exponential relationship was chosen in order to ensure that the function approaches zero asymptotically and is thus non-negative at high temperatures. This assumption is in line with work in the literature which suggests that there is no need for separate fast and slow kinetic pathways at high temperatures [30]. It is noted that as temperature decreases, the magnitude of α(T) increases rapidly (exponentially), and hence, the formulation presented in Equation 14 is not suitable at lower temperatures. Further experimentation is required to determine an expanded temperature profile for α(T), and without this information, it is difficult to assume the functional form of temperature dependence at temperatures outside the scope of the experimental work conducted here (110°C to 170°C).
It is observed that at both temperatures, the model predictions compare reasonably well to the experimental results. It can be seen that the model predictions appear to be slightly shifted (in time) to the right of the experimental results; however, this was expected given that the long heat up time in the experimental set-up caused the experimental data to reflect that a significant amount of hydrolysis had already occurred by t=0.
The results in Figure 9 suggest that the model described in Equations 1 to 5 and 8 to 10, with boundary conditions given by Equation 11 and an initial condition as specified in Equation 12, and with parameters from Equations 6 and 14 is a useful tool for accurately predicting the yield of hemicellulose obtained from the acid pretreatment of sugarcane bagasse.
Conclusions
A novel mathematical model of the hydrolysis of sugarcane bagasse has been developed in this study that uses population balance kinetics to describe chain degradation, diffusion to account for mass transport of soluble oligomers in solution and conservation of volume arguments to account for the change in porosity of the fibrous material caused by the solubilisation of solid xylan chains. Experimental yield profiles were obtained for the dilute acid hydrolysis of hemicellulose oligomers (X _{2}– X _{6}) as well as xylose and furfural. The experimental data obtained was used to calibrate the model by elucidating unknown parameter values through parameter fitting.
Careful consideration must be given to the interpretation of parameters obtained from model fitting when only a single set of data (for example, xylose yield) is used to constrain the fit. The robustness of an acid hydrolysis model can be determined by comparing the model generated yield profiles to a more stringent set of fitting criteria. Such an exercise has been undertaken in this work where the model fit was constrained by oligomer profiles for xylobiose through xylohexaose, in addition to the typical xylose and furfural data sets.
The results showed that adapting “hard-to-hydrolyse” dynamics for a population balance model of acid hydrolysis appears to be able to reproduce yield profiles of not only xylose and furfural but also short-chain oligomers with some degree of accuracy. The model also showed some predictive capability in approximating yield profiles at higher temperatures, where the experimental data was compromised by the heating time of the experimental equipment.
The model presented here has reproduced laboratory scale experimental results. To apply such a model to an industrial “reactor” scale would be largely beneficial in reducing the number of resource intensive hydrolysis experiments required to determine optimal reactor conditions. Further investigation is needed to determine the applicability of this model on such a scale. Although the model appears to capture the chemistry of acid hydrolysis, the industrial scale poses new challenges specific to the reactor design, and some assumptions made at the laboratory scale may need to be revisited. Reactor scale data is needed before any judgements can be made about scaling up this model.
Methods
Materials
Sugarcane bagasse was collected from Racecourse Sugar Mill (Mackay Sugar Limited) in Mackay, Australia. Sugarcane bagasse was washed with hot water at 90°C to remove residual sugars to a negligible amount. The washed sugarcane bagasse was air-dried and gently shaken on a sieve having an aperture size of 1.0 cm to remove pith, and the residues were ground by a cutter grinder (Retsch®; SM100, Retsch GmBH, Germany). The milled bagasse was screened, and particles having width range of 0.5 to 1.0 mm were collected and stored for acid hydrolysis. The water mass fraction of the sieved bagasse sample was 6.3 %. The mass fractions of glucan, xylan, arabinan, lignin, acetyl and ash in the dry bagasse sample were 43.8 %, 20.2 %, 3.3 %, 27.5 %, 2.5 % and 2.1 %, respectively [34]. Sulphuric acid (98 %, mass fraction), xylose (analytical standard) and furfural (99 %, mass fraction) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Xylan oligomers standards (xylobiose, xylotriose, xylotetraose, xylopentaose and xylohexaose) were purchased from Megazyme (Bray, Wicklow, Ireland).
Acid hydrolysis of bagasse samples
Acid hydrolysis of sugarcane bagasse was conducted with a Dionex™ ASE™ 350 Accelerated Solvent Extractor system (Thermo Scientific, Waltham, MA, USA). A glass fibre was placed to the bottom of a 66-mL Dionium™ cell before loading bagasse to the cell. Afterwards, the cell was loosely packed with 5.00 g of milled sugarcane bagasse (4.68-g dry mass). The cell was automatically placed into the oven preheated to the required temperature. Dilute acid (0.5 % H_{2}SO_{4}, mass fraction) was pumped to fill the cell, and the reaction time was counted when the automated cell heat up time had finished. The dilute acid volume pumped into the cell was recorded, which varied slightly between different batches. The temperature used for acid hydrolysis was in a range of 110°C to 170°C in increments of 15°C. After hydrolysis, the cell was purged with nitrogen for 60 s to drain the hydrolysate. The mass of the hydrolysate was recorded. The hydrolysate was stored at −20°C for analysis.
Determination of xylose oligomer concentrations
High-performance liquid chromatography (HPLC) systems were used to determine concentrations of xylose, xylose oligomers and the xylose degradation product (furfural). One HPLC system (Waters, Milford, MA, USA) equipped with a RPM monosaccharide column (300 × 8.0 mm, Phenomenex, Lane Cove, NSW, Australia), a pump (Waters 1515), a refractive index (RI) detector (Waters 410) and an autosampler (Waters 2707) was used to determine xylose in acid hydrolysed samples. The samples were neutralised with CaCO _{3} prior to HPLC analysis. The temperature for both columns was 85°C and the mobile phase was water, with a flow rate of 0.5 mL min ^{−1}. The other HPLC system equipped with an Aminex HPX-87H column (300 × 8.0 mm, Bio-Rad, Richmond, CA, USA), an integrated pump and autosampling system (Waters e2695) and a RI detector (Waters 410) was used to determine xylose degradation product furfural. The samples subjected to determination of furfural were not neutralised. The column temperature was 65°C and the mobile phase was 5 mmol L ^{−1} H _{2} SO _{4}, with a flow rate of 0.6 mL min ^{−1}. Xylose oligomers in pretreatment solution were detected by the HPLC system (Waters, Milford, MA, USA) equipped with a Dionex CarboPac™ PA-100 column (BioLCTM 4 × 250 mm, Thermo Scientific, Waltham, MA, USA), an electrochemical detector (Waters 2465) and the pump and autosampling system (Waters e2695, Milford, MA, USA). The mobile phase consisted of solvent A (150 mmol L ^{−1} NaOH) and solvent B (150 mmol L ^{−1} sodium acetate and 150 mmol L ^{−1} NaOH). The column was run at 30°C with a flow rate of 1 mL min ^{−1} using the gradient method according to curve 6 based on the detection waveform from Dionex Technical Note 21 (Thermo Scientific, Waltham, MA, USA). The gradient method started at 86.7 % solvent A and 13.3 % solvent B (0 to 1 min). The volume ratio of A to B was changed to 0 % : 100 % over 1 to 30 min, to 86.7 % to 13.3 % over 30 to 32 min and maintained at this ratio over 32 to 40 min.
Calculation of furfural, xylose and xylose oligomer yields
Numerical methods
The model equations are formed in terms of two continuous variables (space, r, and time, t) and one discrete variable (chain length, i). The equations were non-dimensionalised, and a vertex-centred finite volume scheme was used to discretise the dimensionless spatial variable, reducing the model to a system of ordinary differential equations (ODEs) in dimensionless time [35]. In MATLAB, the SUNDIALS IDA solver was used to implement the discretised differential algebraic equation (DAE) system [36]. The spatial domain consisted of 100 uniformly spaced nodes in the fibre and 250 uniformly spaced nodes in the hydrolysate. The code was vectorised for efficiency in MATLAB, and the banded structure of the Jacobian was utilised to improve runtime and facilitate a real-time implementation of the parameter fitting algorithm. The run time of a single iteration of the code was a few minutes on a desktop PC.
Parameter fitting was completed using the model independent parameter estimation tool (PEST) [31]. The PEST programme was used to identify values of the rate parameters k _{ a }, k _{ b }, k _{ d } and α that produce a fit of the model results to the experimental data at each temperature. For each temperature, the unknown parameters were varied to find the best simultaneous fit of the model yields to a series of oligomer profiles encompassing furfural, xylose and oligomers up to six chain lengths long. The PEST inputs include a template file (.tpl), an input file (.inp), an instruction file (.ins), a parameter value file (.par) and model output file (.out), which were created manually. PEST also requires a model executable file. The observation file (.obf) and the control file (.pst) were created using the INSCHEK and PESTGEN commands, respectively. The control file was edited such that NOPTMAX =30, PHIREDSTP =0.005, NPHISTP =4, NPHINORED =4, RELPARSTP =0.005 and NRELPAR =4 to more closely align with the recommended control data values in the PEST manual. A relative increment of 0.01 was chosen; however, an increment lower bound (DERINCLB) was specified for each parameter due to the small magnitude of the parameters. The parameters themselves were given a zero lower bound to prevent them from becoming negative, and an upper bound to prevent non-physical values. All observation data points were given equal weighting in the least squares calculation. Spline interpolation was used to find model values at the experimental time points, using MATLAB’s inbuilt interp1 function. An Arrhenius plot was used to find the temperature-dependent form of the rate parameters as discussed in the Results section, and excel was used to find the exponential form of α(T).
Declarations
Acknowledgements
The authors would like to gratefully acknowledge the technical assistance of Shane Russell from Queensland University of Technology’s Institute for Future Environments lab. We would also like to acknowledge Dr. Jayantha Pasdunkorale for his assistance in setting up the PEST framework. Computational resources and services provided by the Queensland University of Technology’s HPC and Research Support Group were used in the production of this manuscript.
Authors’ Affiliations
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