Fractionation of Lignocellulosic Biomass using the OrganoCat Process

Summary

OrganoCat is a method for the pretreatment and fractionation of lignocellulose under mild conditions into lignin, fermentable sugars, and cellulose pulp. In a biogenic, biphasic solvent system of water and 2-methyltetrahydrofuran with 2,5-furancarboxylic acid as catalyst, the OrganoCat products are separated in situ for straightforward product recovery.

Abstract

The shift from a petroleum-based to a more sustainable and bio-based economy requires the development of new refinery concepts to maintain the supply of raw materials and energy. For these novel and sustainable biorefinery concepts, it is important to use catalysts and solvents that are aligned with the principles of Green Chemistry. Therefore, the implementation of biogenic alternatives can be a promising solution. The lignocellulose pretreatment and fractionation process presented herein-OrganoCat-is an integrated fractionation of lignocellulose into its main components using biogenic acids such as 2,5-furandicarboxylic acid as catalyst. Hemicelluloses and other non-cellulosic polysaccharides are selectively depolymerized by the diluted acid and dissolved, while the crystalline cellulose remains in the solid pulp. In the presence of a second organic phase consisting of biogenic 2-methyltetrahydrofuran, disentangled lignin is extracted in situ. The process allows for the efficient fractionation of the three main components-lignin, cellulose, and non-cellulosic sugars. This helps to focus on the quality of the lignin, the improvement of enzymatic hydrolysis of the cellulose-enriched pulp, and the mild non-cellulosic sugar extraction with low degradation.

Introduction

The use of fossil resources has brought great technological advances as they form the basis for numerous products that are essential for everyday life. However, the limitation of resources such as oil and gas on earth and the environmental damages connected with their exploitation create an urgent need for alternatives. Lignocellulosic biomass is a promising source for carbon-based chemicals, as it is renewable, versatile, and carbon neutral¹. Lignocellulose basically consists of three main fractions to make use of: hemicelluloses, cellulose, and lignin. Its industrial processing has a long history. However, established and widespread processes, such as the sulfite and Kraft processes from paper industry, mainly focus on cellulose for utilization in the pulp and paper industry². A full valorization of all three lignocellulosic fractions is needed to make lignocellulose processing towards chemicals more profitable from economic and environmental perspectives.

In many lignocellulose valorization strategies, lignin is a mere byproduct that is often burned for energy recovery. Currently, only 1-2% of the industrially produced lignin is used to produce value-added products such as concrete additives, surfactants, and vanillin³. Nevertheless, it is the largest renewable source of aromatics and therefore has promising properties for application as a basis for polymers⁴, carbon fibers⁵, and fuel². The challenges in the valorization of lignin lie in its complex structure and diversity, depending on the source material and extraction conditions. Moreover, due to their process conditions, the most prevalent lignocellulose fractionation processes deliver sulfonated lignin with a high number of C-C linkages between the monomer units. Therefore, commercially available lignin is challenging to depolymerize.

A range of different approaches, which focus on the holistic utilization of all three fractions, have been developed for lignocellulose fractionation. Most processes rely on the hydrolysis of hemicellulose, either with diluted acids and bases or by utilizing the autoprotolysis of water at elevated temperatures. As one of the most explored options, organosolv processes use low-boiling organic solvents, usually in combination with water. Well-known variants of this process include the Alcell process, which utilizes 50% ethanol, and the Organocell process, which uses methanol in the first step and adds NaOH in the second step. Acid organosolv processes that use formic or acetic acid are also described². Owing to the recent focus on the valorization of lignin as a major biorefinery product, new approaches have been developed, which combine lignin extraction with subsequent or integrated conversion steps to yield smaller lignin compounds and more stable and valuable products^6,7,8.

The OrganoCat lignocellulose fractionation process (OrganoCat) is based on a two-phase system of water and 2-methyltetrahydrofuran (2-MTHF)⁹. Additionally, a recyclable organic acid is used as catalyst, which selectively hydrolyzes hemicelluloses at mild temperatures. All process chemicals can be produced in a relatively inexpensive and biogenic manner, which lowers the environmental impact of the process in accordance to the principles of Green Chemistry¹⁰. The process delivers three separate product streams with lignin in the organic phase, depolymerized hemicellulose sugars in the aqueous phase, and cellulose-enriched pulp as a solid residue. As the product streams can be easily separated, downstream steps, energy demand, and material costs can be reduced significantly compared to, for example, monophasic approaches. The lignin has a relatively low molecular weight and a high number of β-O-4 linkages¹¹. The depolymerized hemicellulose sugars can be used for fermentation or conversion into fine chemicals¹². The cellulose pulp is highly accessible for enzymatic depolymerization⁹.

The original OrganoCat process uses oxalic acid as catalyst to fractionate lignocellulose. Oxalic acid can then be recovered by crystallization⁹. However, this increases the process costs for cooling the reaction and the partial evaporation of water. The partial decomposition of oxalic acid would diminish the revenues further¹³. For this reason, the OrganoCat process was improved by introducing 2,5-furandicarboxylic acid (FDCA) as catalyst¹¹. FDCA is not only sufficiently acidic to catalyze the reaction, but can also be derived from glucose via dehydration to 5-hydroxymethylfurfural and subsequent oxidation with metal-based catalysts or biocatalysts^14,15,16,17. Although the acidity of FDCA is slightly lower, it has a higher thermal stability than oxalic acid. FDCA has a low solubility in water at room temperature, which allows its straightforward recovery from the aqueous phase after the reaction.

A scale-up of the OrganoCat process was successfully developed to a 3 L reactor¹⁸. Additional studies on OrganoCat lignin found that antisolvent precipitation with n-hexane or n-pentane allow an energy efficient lignin recovery¹⁹. It was possible to get lignin fractions with different molecular weights²⁰. This paper presents the full preparative method for a scalable, one-step fractionation process of lignocellulosic biomass using FDCA as catalyst. This process yields extracted lignin, depolymerized hemicelluloses, and cellulose pulp in three easily separable product streams.

Protocol

NOTE: The process may be paused at any point by leaving the samples at room temperature (for a few days) or in the refrigerator (for longer periods). See the Table of Materials for details on the materials used in this protocol.

1. Beech wood particles

1. Generate the desired particle size of beech wood (Fagus sp.) using a cutting mill with a 10 mm sieve, and dry the particles at 50 °C to constant mass (~24 h), leaving a residual moisture content of ~10% water.

2. Lignocellulosic fractionation and workup

1. Lignocellulose pretreatment and fractionation
   1. Suspend 500 mg of beech wood (Fagus sp.) particles and 78.0 mg (0.5 mmol, 0.1 M) of FDCA in 5 mL of ultrapure water at room temperature in a 25 mL stainless steel high-pressure reactor. Add 5 mL of 2-MTHF and a stirring bar to the suspension, and close the reactor. Heat the reactor to 160 °C on a heating plate at a stirring speed of 1500 rpm for 1 h.
   2. Let the reaction cool down to room temperature in ice-water over a period of ~10 min. Open the reactor, add 52.5 µL of NaOH solution (50 wt% NaOH in distilled water), and stir for 15 min at room temperature and 500 rpm on a stirring plate.
2. Isolation of organic phase and lignin quantification
   1. Centrifuge the mixture (room temperature, 5 min, 1880 × g). Use a pipette to transfer the organic phase (2-MTHF) to a 50 mL round-bottom flask.
   2. Evaporate the organic phase in a rotary evaporator (40 °C, 200 rpm, 180 mbar) until a solid and dry lignin fraction is obtained. Determine the lignin yield by weighing with an analytical balance. Store the solid lignin at room temperature for further analysis.
3. Separation of solid cellulose-enriched pulp and aqueous phase
   1. Filter the aqueous phase using a cellulose filter paper (17-30 µm pore size) in a funnel to isolate the cellulose-enriched pulp, and transfer the aqueous phase to a 5 mL vial. Wash the pulp until neutral pH with 3 x 25 mL water, and store the washing solution separately in a 100 mL beaker. Dry the pulp at 80 °C to constant mass (~24 h).
   2. Determine the dried pulp yield by weighing with an analytical balance.
4. FDCA recovery and isolation of aqueous phase
   1. Adjust the pH of the aqueous phase and the washing solution from step 2.3 separately under constant stirring to pH 1 using concentrated HCl while cooling the solution in an ice bath. Control the pH using universal indicator paper.
   2. Filter the precipitated solid (FDCA) from both solutions, combine the residues, and dry at 80 °C to constant mass (~24 h). Discard the washes. Determine the FDCA yield by weighing with an analytical balance.
   3. Transfer the aqueous phase to a 25 mL flask, and store it at 4 °C for analysis.
5. Sample preparation for furfural quantification
   1. Perform a separate experiment to determine the quantity of furfural. Repeat steps 2.1.1-2.2.1.
   2. Add 40 mg of n-decane as an internal standard to the collected organic solvent fraction, and store for analysis.

3. Analysis

1. Analysis of sugar in the aqueous phase by high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD)
   1. Dilute 10 µL of the aqueous phase collected in step 2.4.3 with 190 µL of distilled water. Add 10 µL of 2 mM 2-deoxy-D-glucose to the diluted sample.
   2. Perform the separation of monosaccharides on a monosaccharide separator column with a flow rate of 0.5 mL∙min^-1, and inject the sample after equilibration with 2 mM NaOH for 10 min. Separate the neutral sugars with 2 mM NaOH over 18 min. Afterwards, use 550 mM NaOH for 10 min to separate the uronic acids. Rinse the column with 800 mM NaOH for 10 min.
      NOTE: The software normalizes the amounts of monosaccharides to the amount of the internal standard and quantifies them by using standard calibration curves of the different monosaccharides.
2. Lignin analysis via ¹H-¹³C heteronuclear single quantum correlation nuclear magnetic resonance (¹H-¹³C-HSQC NMR)
   1. Dissolve ~50 mg of lignin in 0.5 mL of deuterated dimethylsulfoxide ([d₆] DMSO), and transfer the mixture to an NMR tube. Conduct ¹H-¹³C HSQC (measurement time 220 min) NMR measurements using a 400 MHz spectrometer.
   2. Determine the types of linkages present in the lignin using the spectrum.
      1. Reference the chemical shift of the spectrum to the DMSO signal (δ(¹H) = 2.500 ppm; δ(¹³C) = 39.52 ppm).
      2. Perform a manual phase correction on both axes until all the signals are positive, then perform a baseline correction.
      3. Integrate the signals of the aromatic units and the linkages of the lignin; see Table 1 for the chemical shifts.
   3. Calculate the sum of the aromatic units (arom.) using the following formula:
      Σ(arom.) = (S_2,6 / 2) + ((G₂ + G₅) / 2) + (H_2,6 / 2) (1)
      ​With S_i being the integral over the signal corresponding to the 2 and 6 syringyl protons, G_i being the integrals over the signals corresponding to the 2 and 5 guaiacyl protons, and H_i being the integral over the signal corresponding to the 2 and 6 p-hydroxyphenyl protons.
   4. Calculate the percentage of each unit using the following formulas:
      S = (S_2,6/ 2) / Σ(arom.) × 100% (2)
      G = ((G₂ + G₅) / 2) / Σ(arom.) × 100% (3)
      H = (H_2,6 / 2) / Σ(arom.) × 100% (4)
      ​With S, G, and H being the percentages of respective monomers-syringyl- (S), guaiacyl- (G), and p-hydroxyphenyl (H)-monomer units per 100 monomer units.
   5. Calculate the number of linkages per 100 units using the following formulas:
      β-O-4 linkages = α β-O-4 / Σ(arom.) × 100% (5)
      linkages = (α β-β + β β-β + γ β-β) / Σ(arom.) × 100% (6)
      linkages = (α β-5 + β β-5 + γ β-5) / Σ(arom.) × 100% (7)
      With α, β, and γ being the integral over the signal corresponding to the α-, β- and γ-proton signals of the corresponding β-O-4-, β-β- and β-5 linkages.
      NOTE: Linkages are given as linkage per 100 monomer units. Due to overlapping of peaks, β-O-4 is calculated using only the α proton signal. β-β and β-5 linkages are calculated using all signals of the corresponding linkage.
3. Gel permeation chromatography (GPC) analysis
   1. Dissolve 10 mg of dried lignin and 1 mg of glucose (as internal standard) in 1 mL of a 0.1 M NaOH and 0.01 wt% NaN₃ aqueous solution in a 1.5 mL gas chromatography (GC)-vial. Close the GC-vial using a cap with septum.
   2. Inject 100 µL of the sample into a high-performance liquid chromatography (HPLC) system equipped with an ultraviolet detector and monitoring a wavelength of λ = 280 nm. Use a system consisting of a precolumn programmed-temperature split/splitless injector system with polar silica (8 mm x 50 mm) and three gel columns (8 mm x 300 mm, particle diameter: 5 µm, nominal pore width: 1000 Å) at a flow rate of 1 mL min^-1. Reference the obtained data to the signal of the internal standard (glucose). Calculate the mass distribution using the software, referenced to an external calibration with poly(styrene sulfonate) in a range from 266 to 65000 Da.
4. Furfural quantification via GC
   1. Add 20 mg n-decane as internal standard to the organic phase of the OrganoCat pretreatment. Transfer 1 mL of the organic phase into a 1.5 mL GC-vial.
   2. Inject 1 µL of this solution into a gas chromatograph using a 30 m column with a polar polyurethane glycol stationary phase and helium as the carrier gas with a flow rate of 1.5 mL min^-1 and a flame-ionization detector. Set the initial temperature to 50 °C, then raise by 8 °C min^-1 to 250 °C and maintain at 250 °C for 5 min.
   3. Quantify furfural using the integrals (Int) given by the software and an externally calculated correction factor (cf).
      1. Prepare a sample of 1 mg of furfural and 5 mg of n-decane in 1 mL of 2-MTHF, and inject it into the GC using the aforementioned procedure. Calculate the correction factor as follows:
         cf = (Int(n-decane) / m(n-decane)) / (Int(furfural) / Int(furfural)) (8)
      2. Use the correction factor to calculate the amount of furfural in the unknown sample with the following formula:
         m(furfural) = m(n-decane) / Int(n-decane) × cf × Int(furfural) (9)
5. Cellulose-enriched pulp hydrolysis
   1. Carry out pulp hydrolysis of cellulose-enriched residue obtained from OrganoCat pretreatment in a heating block with mixing (see the Table of Materials) using 1.5 mL vials.
   2. Add 20 mg of cellulose-enriched pulp and 10 µL of cellulase (60 filter paper units (FPU) mL^-1 and 82 cellobiase units (CBU) mL^-1) to 1 mL of citrate buffer (pH = 4.5) in a 1.5 mL vial, and shake at 50 °C for 0 h, 1 h, or 72 h. Afterwards, heat the samples to 99 °C for 10 min to denature the enzymes.
   3. Determine the glucose concentration using a glucose (hexokinase) assay kit.

Results

A typical set of conditions for the lignocellulose pretreatment and fractionation process OrganoCat (OrganoCat) uses 0.1 M FDCA as a catalyst, a biomass loading of 100 g L^-1 (beech wood, compared to the aqueous phase), 1 h of reaction time and 160 °C as the reaction temperature. The composition of beech wood has been published elsewhere²¹ (~48% cellulose, 27% hemicellulose, 26% lignin). Figure 1 shows the extracted hemicellulose hydrolysate with this set of conditions as well as longer reaction time (3 h) and lower temperature (140 °C).

Using harsher conditions, e.g., higher temperature and longer reaction time, might lead to higher extraction yields, but also leads to more degradation of the products-furfural is a degradation product of xylose, whereas 5-(hydroxymethyl)furfural (5-HMF) is the corresponding degradation product of glucose. A higher amount of furfural was noted in the products (distributed between the aqueous and the organic phases) with a reaction time of 3 h at 160 °C. As the sugar degradation products are highly reactive and tend to form humins-oligomers of furans and sugars-the shorter reaction time at higher temperature might be considered a good compromise between high extraction efficiency and low sugar degradation.

The amount of extracted lignin is directly related to the reaction temperature and time as well. Figure 2 displays the amount of lignin extracted, the β-O-4-linkage content, and the mass-average molar masses of the extracted lignins. While the extracted lignin yield rises with longer reaction time, the number of intact β-O-4-linkages diminishes by approximately half when reacting for 3 h instead of 1 h. Lowering the reaction temperature from 160 °C to 140 °C has a much lower impact on lignin, resulting in slightly less yield, smaller mass-average molar mass, and higher β-O-4-content.

As enzymatic hydrolysis of (lingo-)cellulose is a common indicator for pulping efficiency, a commercial cellulose cocktail was applied to the different OrganoCat pulps resulting from the above mentioned OrganoCat reaction condition sets (Figure 3). As the cellulase is not optimized for the substrates, the overall cellulose conversion is not comparable to state-of-the-art performance; however, it allows the comparison of the different pulps to each other. The longer reaction time exhibits a significant impact on the initial reaction time and the glucose yield after 72 h, improving by a factor of ~2.5. Lowering the temperature appears to show a much smaller impact, implying that the main factor causing the differences in enzymatic digestibility within this treatment is the degree of delignification.

Figure 1: Sugar extraction and furfural production in OrganoCat process with 0.1 M 2,5-furandicarboxylic acid as catalyst and 100 g L^-1 beech wood (compared to the aqueous phase) at different reaction temperatures and times as indicated on the x-axis¹¹. All experiments have been performed in triplicate. The average is shown with the standard deviation. Please click here to view a larger version of this figure.

Figure 2: Amount and analysis of lignin extracted by OrganoCat process with 0.1 M 2,5-furandicarboxylic acid as catalyst and 100 g L^-1 beech wood (compared to the aqueous phase) at different reaction temperatures and times as indicated on the x-axis¹¹. Lignin yields have been calculated in triplicate. The average is shown with the standard deviation. Molecular mass and linkages were derived from representative single experiments. Please click here to view a larger version of this figure.

Figure 3: Enzymatic hydrolysis of pulps. Glucose yields after 72 h (blue bars) and reaction rates within the first hour (gray bars) from the hydrolysis of untreated beech wood and cellulose-enriched pulps obtained from OrganoCat with 0.1 M 2,5-furandicarboxylic acid as catalyst and 100 g L^-1 beech wood (compared to the aqueous phase) at different reaction temperatures and times as indicated on the x-axis. Cellulase was applied to the different substrates at 50 °C for up to 72 h in contrite buffer (pH 4.5)¹¹. All experiments have been performed in triplicate. The average is shown with the standard deviation. Please click here to view a larger version of this figure.

Unit	Shift δ (1H)(13C)	Linkage	Shift δ (1H)(13C)
	[ppm]		[ppm]
S2,6	(6.95–6.46)(106.8–101.9)	α β-O-4	(5.08–4.69)(75.8–69.9)
G2	(7.12–6.72)(113.4–108.7)	α β-β	(4.72–4.58)(87.46–84.0)
G5	(7.04–6.51)(117.8–113.4)	β β-β	(3.35–3.11)(62.0–57.9)
H2,6	(7.01–6.8)(129.1–123.2)	γ β-β 1	(4.26–4.09)(73.0–70.0)
		γ β-β 2	(3.87–3.71)(73.0–70.0)
		α β-5	(5.51–5.41)(88.8–86.6)
		β β-5	(3.52–3.42)(54.0–52.1)
		γ β-5	(3.80–3.67)(64.1–62.1)

Table 1: Chemical shifts determined by ¹H-¹³C heteronuclear single quantum correlation nuclear magnetic resonance (¹H-¹³C-HSQC NMR) for different linkages in lignin. Abbreviations: S = syringyl unit, G = guaiacyl unit, H = p-hydroxyphenyl unit.

Discussion

The described fractionation of lignocellulose shows a tradeoff between hemicellulose hydrolysis efficiency and selectivity to avoid sugar degradation to furans, depending on reaction time and temperature (Figure 1). Lignin extraction was similarly affected by the harsher conditions. Especially the reduction of β-O-4-linkages and enhancement of mass average molecular weight due to recondensation at higher temperature and reaction time underlines this compromise that must be made. The selection of reaction time and temperature is therefore a critical step in this lignocellulose fractionation process. As the efficiency of enzymatic hydrolysis appears to be mostly determined by delignification in the FDCA-catalyzed OrganoCat process, the harshest processing conditions afford the most accessible pulp. Other variations of the process^9,11,18,22, e.g., using different catalysts, show that the strength of the catalyst and the final pH in the reactive solution have the strongest effect on process efficiency. Modifications of the procedure, e.g., preswelling with phosphoric acid, have been shown to have a beneficial effect as well²². Due to the variety in composition, however, the process needs optimization, depending on the different feedstocks²¹. Considering the overall process performance, downstream purification of the separated fractions must be considered, which is why selectivity plays a major role. Compared to other organosolv-like processes, OrganoCat uses a biphasic water/2-MTHF system, which affords the major components in three relatively straightforward, separate streams. This way, further downstream and resulting energy and equipment costs can be reduced^13,18.

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
1200 HPLC system	Agilent	n.a.	was used for size exclusion chomatogaphy
2,5-furandicarboxylic acid	TCI Deutschland GmbH	F0710	Purity: >98.0%(T)(HPLC)
2-methyltetrahydrofuran	Carl Roth GmbH	6845.4	SOLVAGREEN ≥99 %, extra pure
Accellerase 1500	Provided by Genencor (60 FPU mL-1 and 82 CBU mL-1; 2300 AE Leiden, Netherlands)	n.a.	cellulase for pulp hydrolysis
beech wood (Fagus sp.)	local supplier	n.a.
BioTek Power Wave HT UV-Vis Spectrometer	BioTek Germany, 74177 Bad Friedrichshall, Germany	BT-RPRWI
Bruker AS400 (400 MHz) Spectrometer	Bruker, Billerica, MA 01821, USA	n.a.	HSQC-NMR analysis
CarboPac PA20 column	Dionex	302747	monosaccharide separator column for high-performance anion-exchange chromatography
centrifuge 5430 R	Eppendorf	5428000610
Focus GC	Thermo Fischer	n.a.	gas chromatograph
Glucose (hexokinase) assay kit	Sigma-Aldrich	GAHK20-1KT
GPC- precolumn PSS PolarSil in DMAc	PSS Polymer Strandards Service GmbH	PSA080505	precolumn with polar silica (8 x 50 mm)
HP-INNOwax column 30 m	Agilent J & W	19091N-213IE	GC column with a polar polyethylene glycol stationary phase
PSS MCX	PSS Polymer Strandards Service GmbH	MCA0830051E3	gel columns (8 x 300 mm, particle diameter: 5 µm, nominal pore width: 1000 Å
ThermoMixer	Eppendorf	n.a.	mixing and heating block
tinyclave steel Typ 3 / 25 mL	Büchi	49,33,45,10,000	100 bar, 200 °C