This document summarizes a study that introduces a new pretreatment method called co-solvent-enhanced lignocellulosic fractionation (CELF) to reduce enzyme requirements for high sugar yields from lignocellulosic biomass. CELF employs THF mixed with dilute acid to pretreat corn stover. The study found that CELF achieved near 95% theoretical sugar yields from corn stover even at very low enzyme loadings of only 2 mg enzyme per g glucan. This was attributed to high lignin removal through CELF pretreatment as supported by compositional analysis, modeling, and imaging. CELF pretreatment also produced solids that when subjected to simultaneous saccharification and fermentation with low enzymes produced
This document summarizes Keith Biggart's Masters research project on the characterization of cellulose degradation products obtained through pressurized hot water extraction. The research involved conducting extractions of cellulose at varying temperatures and catalytic conditions. Analytical techniques like FT-IR, DLS, HPLC-MS, LC-MSn, GC-MS were used to qualitatively characterize the extracts. The results showed increased cellulose conversion and smaller molecule sizes in the extracts at higher temperatures. Static extractions and use of metal catalysts further improved degradation. Platform chemicals like furfural and dimethylfuran were identified in extracts processed at over 250°C, indicating PHWE is an environmentally friendly method for cellulose degradation.
This document summarizes a study that assessed the biogas production potential of co-digesting various fruits, vegetables, and mixtures. Batch experiments were conducted in lab-scale reactors to co-digest combinations of substrates. Kinetic models were applied to analyze degradation performance and biogas production, including first-order, two-step, and two-pool models. The models fit the observed biogas production data well. Estimated kinetic constants were similar for vegetable digestion and co-digestion with oil but significantly higher for fruit co-digestion, indicating faster degradation. The study provides insights into kinetics of co-digestion processes.
Synthesis of customized petroleum-replica fuel molecules by targeted modifica...biocenose_consultoria
1) Researchers engineered E. coli to produce fuel-like hydrocarbons by expressing genes that utilize free fatty acids as substrates for alkane biosynthesis, allowing the hydrocarbon output to be tailored.
2) Expression of genes from Photorhabdus luminescens and Nostoc punctiforme enabled E. coli to produce a variety of linear and branched alkanes and alkenes matching the carbon chain lengths of diesel and aviation fuels.
3) Modifying the fatty acid pool through genetic modifications or exogenous supplementation successfully altered the hydrocarbon output in predictable ways, demonstrating the ability to design microbial pathways for producing industrially relevant fuel molecules.
This document summarizes a study that used tetrahydrofuran (THF) as a co-solvent to enhance the production of fuel precursors like furfural, hydroxymethylfurfural (HMF), and levulinic acid from maple wood biomass. Key findings include:
1) THF allowed over 90% of lignin to be extracted from maple wood while hydrolyzing it to sugars, achieving higher yields of fuel precursors than water alone.
2) A maximum overall yield of 87% of theoretical fuel precursors from C5 and C6 sugars was achieved using a THF to water ratio of 1:1.
3) Solids remaining after THF treatment were highly digestible
Kinetics and feasibility studies of thiol oxidation using magnetically separa...Pawan Kumar
This work describes kinetic studies of the catalytic oxidation of thiols (RSHs) found in kerosene to disulphides using a magnetically separable iron oxide coated Mg-Al layered double hydroxide supported tetra-sulphonated cobalt phthalocyanine (CoPcS/LDH@Fe3O4) catalyst in an alkali-free environment. Using 1-octanethiol as a representative RSH, we investigated the effects of different experimental parameters on RSH oxidation kinetics, including catalyst concentration, temperature (30–60 °C), and initial thiol concentration ([RSH]0, 100–300 ppm). The catalyst concentration was varied so that the [RSH]0/[Co]tot molar ratio ranged from 45 to 180. Based on the results, we propose a mechanistic rate expression to explain the observed oxidation of RSH in the presence of the CoPcS/LDH@Fe3O4 catalyst. The proposed rate law resembles double substrate Michaelis-Menten kinetics, however, for commonly …
Sunlight-driven water-splitting using two-dimensional carbon based semiconduc...Pawan Kumar
The overwhelming challenge of depleting fossil fuels and anthropogenic carbon emissions has driven research into alternative clean sources of energy. To achieve the goal of a carbon neutral economy, the harvesting of sunlight by using photocatalysts to split water into hydrogen and oxygen is an expedient approach to fulfill the energy demand in a sustainable way along with reducing the emission of greenhouse gases. Even though the past few decades have witnessed intensive research into inorganic semiconductor photocatalysts, their quantum efficiencies for hydrogen production from visible photons remain too low for the large scale deployment of this technology. Visible light absorption and efficient charge separation are two key necessary conditions for achieving the scalable production of hydrogen from water. Two-dimensional carbon based nanoscale materials such as graphene oxide, reduced …
This document summarizes Keith Biggart's Masters research project on the characterization of cellulose degradation products obtained through pressurized hot water extraction. The research involved conducting extractions of cellulose at varying temperatures and catalytic conditions. Analytical techniques like FT-IR, DLS, HPLC-MS, LC-MSn, GC-MS were used to qualitatively characterize the extracts. The results showed increased cellulose conversion and smaller molecule sizes in the extracts at higher temperatures. Static extractions and use of metal catalysts further improved degradation. Platform chemicals like furfural and dimethylfuran were identified in extracts processed at over 250°C, indicating PHWE is an environmentally friendly method for cellulose degradation.
This document summarizes a study that assessed the biogas production potential of co-digesting various fruits, vegetables, and mixtures. Batch experiments were conducted in lab-scale reactors to co-digest combinations of substrates. Kinetic models were applied to analyze degradation performance and biogas production, including first-order, two-step, and two-pool models. The models fit the observed biogas production data well. Estimated kinetic constants were similar for vegetable digestion and co-digestion with oil but significantly higher for fruit co-digestion, indicating faster degradation. The study provides insights into kinetics of co-digestion processes.
Synthesis of customized petroleum-replica fuel molecules by targeted modifica...biocenose_consultoria
1) Researchers engineered E. coli to produce fuel-like hydrocarbons by expressing genes that utilize free fatty acids as substrates for alkane biosynthesis, allowing the hydrocarbon output to be tailored.
2) Expression of genes from Photorhabdus luminescens and Nostoc punctiforme enabled E. coli to produce a variety of linear and branched alkanes and alkenes matching the carbon chain lengths of diesel and aviation fuels.
3) Modifying the fatty acid pool through genetic modifications or exogenous supplementation successfully altered the hydrocarbon output in predictable ways, demonstrating the ability to design microbial pathways for producing industrially relevant fuel molecules.
This document summarizes a study that used tetrahydrofuran (THF) as a co-solvent to enhance the production of fuel precursors like furfural, hydroxymethylfurfural (HMF), and levulinic acid from maple wood biomass. Key findings include:
1) THF allowed over 90% of lignin to be extracted from maple wood while hydrolyzing it to sugars, achieving higher yields of fuel precursors than water alone.
2) A maximum overall yield of 87% of theoretical fuel precursors from C5 and C6 sugars was achieved using a THF to water ratio of 1:1.
3) Solids remaining after THF treatment were highly digestible
Kinetics and feasibility studies of thiol oxidation using magnetically separa...Pawan Kumar
This work describes kinetic studies of the catalytic oxidation of thiols (RSHs) found in kerosene to disulphides using a magnetically separable iron oxide coated Mg-Al layered double hydroxide supported tetra-sulphonated cobalt phthalocyanine (CoPcS/LDH@Fe3O4) catalyst in an alkali-free environment. Using 1-octanethiol as a representative RSH, we investigated the effects of different experimental parameters on RSH oxidation kinetics, including catalyst concentration, temperature (30–60 °C), and initial thiol concentration ([RSH]0, 100–300 ppm). The catalyst concentration was varied so that the [RSH]0/[Co]tot molar ratio ranged from 45 to 180. Based on the results, we propose a mechanistic rate expression to explain the observed oxidation of RSH in the presence of the CoPcS/LDH@Fe3O4 catalyst. The proposed rate law resembles double substrate Michaelis-Menten kinetics, however, for commonly …
Sunlight-driven water-splitting using two-dimensional carbon based semiconduc...Pawan Kumar
The overwhelming challenge of depleting fossil fuels and anthropogenic carbon emissions has driven research into alternative clean sources of energy. To achieve the goal of a carbon neutral economy, the harvesting of sunlight by using photocatalysts to split water into hydrogen and oxygen is an expedient approach to fulfill the energy demand in a sustainable way along with reducing the emission of greenhouse gases. Even though the past few decades have witnessed intensive research into inorganic semiconductor photocatalysts, their quantum efficiencies for hydrogen production from visible photons remain too low for the large scale deployment of this technology. Visible light absorption and efficient charge separation are two key necessary conditions for achieving the scalable production of hydrogen from water. Two-dimensional carbon based nanoscale materials such as graphene oxide, reduced …
1) Self-assembled monolayer coated gold nanoparticles catalyze the aerobic oxidation of alpha-hydroxy ketones to aryl 1,2-diketones in water.
2) This provides an efficient one-pot synthesis of quinoxaline derivatives by in situ oxidation of alpha-hydroxy ketones and subsequent condensation with aryl 1,2-diamines in water.
3) 4-Aminothiophenol self-assembled monolayer coated gold nanoparticles were found to be an effective catalyst for these reactions, providing good to excellent yields of products under mild conditions in water.
1) A one-pot synthesis of novel 9-aminoacridine derivatives is described using simple nucleophilic aromatic substitution and addition-elimination reactions with readily available starting materials.
2) Two general reaction conditions are established - refluxing in ethanol overnight or using cesium carbonate in DMF at 90°C for 12 hours. These methods give moderate to good yields of various substituted 9-aminoacridine derivatives.
3) Specifically, 9-(azaarylamino)acridines are synthesized from chloropyridines and chloropyrimidines via SNAr reactions. 9-(Acridinylamino)quinones are also synthesized from haloquinones and halo naphtho
This document discusses hydrogen delivery through liquid organic hydrides (LOH) such as cycloalkanes. It covers considerations for this potential technology, including dehydrogenation catalysts, catalyst supports, and reaction kinetics and thermodynamics. Key points include: (1) Cycloalkanes such as cyclohexane and methylcyclohexane can store 6-8% hydrogen by weight and are liquid at ambient conditions, making them suitable for hydrogen transport. (2) Dehydrogenation over metal catalysts such as Pt is an effective way to release hydrogen from the hydrides. (3) Pt-based catalysts generally have the highest activity and selectivity, while bi-metallic catalysts may have even higher activity through synergistic effects
This document summarizes research on developing an orthogonal fatty acid biosynthesis system in E. coli for oleochemical production. Key findings include:
- Several type I fatty acid synthase (FAS) enzymes from Corynebacterium glutamicum and Mycobacterium tuberculosis were cloned and expressed solubly in E. coli.
- The activity of several type I FAS enzymes was demonstrated in vivo, and C. glutamicum FAS was used to produce fatty alcohols and methyl ketones.
- This represents the first example of a heterologous FAS pathway in E. coli and lays the groundwork for further optimizing renewable oleochemical production.
This study evaluated the biodegradability of the antioxidant diaryl-p-phenylene diamine (DAPD) using a modified inherent biodegradation test. DAPD is used in tires and rubber products. Previous studies found it was not readily biodegradable using standard tests. This study used radiolabeled DAPD (R-898) at low concentrations of 10-100 μg/L added to silica gel to enhance solubility, along with a surfactant. After 28 days, no parent compound remained. After 63 days, 37% had mineralized and 29% was incorporated into biomass, demonstrating biodegradation. The modifications enhanced the sensitivity of the test to show DAPD
This document describes research on the heterologous expression of an NADP-dependent [NiFe]-hydrogenase from Pyrococcus furiosus in Escherichia coli. The researchers were able to successfully produce a functional form of the recombinant hydrogenase enzyme by co-expressing 13 P. furiosus genes involved in hydrogenase maturation in E. coli. Remarkably, providing only the four structural genes encoding the hydrogenase subunits and a single protease from P. furiosus was sufficient for the native E. coli maturation machinery to generate functional hydrogenase. This demonstrates that E. coli can assemble a functional hydrogenase from a phylogenetically distant hyperthermophilic organism.
Liquid crystal bio-based epoxy coating with enhanced performanceIJERA Editor
Tetrafunctional rosin based epoxy was synthesized and cured with either rosin based hardener or conventional
phenylene diamine to study the feasibility of producing high performance thermosetting polymer from
renewable resource. The chemical structure of the prepared epoxy was confirmed by elemental analysis, FTIR,
1HNMR, UV, total acid number and epoxy equivalent weight. Dynamic mechanical (DMA) and
thermogravimetric (TGA) analyses results indicate that fully biobased epoxy system possesses high glass
transition temperature (Tg), high modulus (G`) and improved thermal stability.
1) An efficient protocol has been developed for the synthesis of biaryls via Pd/Cu catalyzed coupling of phenylhydrazines in water without using any ligands.
2) Both Pd and Cu catalysts were found to be essential for the reaction, with Pd(TFA)2 and Cu(OAc) providing the best results.
3) A range of substituted phenylhydrazines underwent homo- and cross-coupling reactions under the optimized conditions to provide the biaryl products in good to excellent yields.
This document discusses an integrated acetic acid based one-pot ethanolamine acetate pretreatment process for efficient depolymerization of poplar polysaccharides. Key points:
(1) The new process simultaneously removes 88% of hemicellulose and extracts up to 46% of lignin from poplar biomass.
(2) It yields over 80% enzyme-hydrolyzed glucose, attributed to increased accessible surface area of cellulose.
(3) Analysis indicates the ionic liquid component is a good lignin solvent, leading to higher delignification.
Overall, integrating ionic liquid with acid pretreatment is a promising strategy for effective pretreatment of woody lignocellulose.
Highly stable pt ru nanoparticles supported on three-dimensional cubic ordere...suresh899
The cost of the catalysts used in the direct methanol fuel cell
poses a challenge to its widespread use as an energy efficient and environment
friendly fuel conversion technology. In this study, two types of highly ordered
mesoporous carbon CMK-8 (I and II) with high surface area and 3-D
bicontinuous interpenetrating channels were synthesized and deposited with
PtRu nanoparticles using the sodium borohydride reduction method. The
electrocatalytic capabilities for methanol oxidation were investigated using
cyclic voltammetry and chronoamperometry, and the results were compared
with that of PtRu deposited on Vulcan XC-72 using the same preparation
method as well as with commercial PtRu/C (E-TEK) catalyst. Pt Ru/CMK-8-I synthesized by the method developed in this work revealed an
outstanding specific mass activity (487.9 mA/mg) and superior stability
compared with the other supports, thus substantiating its potential to reduce
the costs of DMFC catalysts.
This document summarizes a student research project analyzing the dose response of cellulase enzyme cocktails under variable temperature, pH, and ionic liquid conditions. The student determined the optimal temperatures and pH levels for different enzymes to catalyze glucose production from cellulose. Initial experiments found optimal temperatures of 65°C and 85°C for enzymes Cel_9A and Cel_5A, respectively. Further experiments analyzed the effects of varying temperature, pH, and ionic liquid concentration on glucose production across different enzyme doses. The goal was to optimize conditions to maximize glucose yields for producing biofuels through fermentation.
Steam pretreatment and acid-catalyzed pretreatment technologies are widely used to make lignocellulose more accessible to enzymatic hydrolysis. During these pretreatments, hemicellulose is partially removed and lignin is redistributed, increasing the surface area and pore volume of the material. This exposes the cellulose microfibrils and makes them more accessible to cellulase enzymes. Still, some technical challenges around maximizing sugar yields and reducing costs remain to be solved before these pretreatment technologies can be commercially viable at large scale.
This document summarizes a study on the hydrothermal dissolution of willow biomass in hot compressed water. The key findings are:
1) A 95% dissolution of willow was achieved at temperatures as low as 200°C and pressures of 10 MPa, with lignin and hemicellulose dissolving first, followed by cellulose between 280-320°C.
2) A proposed dissolution mechanism involves the rapid fragmentation and hydrolysis of lignin, hemicellulose, and cellulose into oligomers and other water-soluble products like glucose.
3) A continuous flow process was found to be more effective for dissolution than a batch process, due to reduced recondensation of dissolved oligomers.
cellulose, the most abundant natural biopolymer, has long been
investigated as a new green source to replace non-renewable materials and chemicals, but its highly ordered hydrogen bond network
and high crystallinity, which both detract cellulose reactivity and
solubility (Kondo, 1998), have made it difficult to exploit the full
potential of cellulose materials. To overcome these problems, many
new solvent systems have been studied to enable the homogeneous
modification of cellulose (Ramos, Frollini, & Heinze, 2005; Wu
et al., 2004). Many modifications are nevertheless still preferably
conducted heterogeneously in an aqueous medium, particularly
because of the advantages of this approach with regard to toxicity,
volatility and price.
One potential react
The document presents a kinetic model for the acid-catalyzed delignification of sugarcane bagasse by aqueous acetic acid (AcH). The model introduces the concept of "potential degree of delignification (dD)" to account for the multilayered structure of plant cell walls and the inhibitory effect of dissolved lignin. Experimental results showed that delignification rate followed first-order kinetics with respect to sulfuric acid concentration but had a high reaction order with respect to AcH concentration. The activation energy for delignification was determined to be 64.41 kJ/mol. Mechanism analysis found that cleavage of α-aryl ether bonds in lignin was mainly responsible for lignin fragment formation, and increasing AcH
This document discusses improving the bioenergy conversion efficiency of food waste through pretreatment, co-digestion, and reactor type selection. Food waste has great potential for methane production through anaerobic digestion but currently suffers from low conversion efficiency due to its long hydraulic retention time, low organic loading rate, and low conversion rate. Pretreatment technologies like enzymatic pretreatment and co-digestion with other wastes can help accelerate hydrolysis of organic solids and enhance methane production. Using a third generation anaerobic reactor along with enzymatic pretreatment and co-digestion of food waste with landfill leachate may allow over 90% of organic matter in food waste to be recovered as bioenergy with an organic loading rate greater
This document summarizes research on the hydrothermal liquefaction of algae feedstocks in a continuous-flow reactor system. Key points:
- Algae can be converted to an upgradeable biocrude through hydrothermal liquefaction at 350°C and 20 MPa in a continuous-flow reactor, without the need for solvents. High carbon conversions were achieved even at high algae concentrations.
- Catalytic hydrotreating was effectively used to upgrade the biocrude through hydrodeoxygenation, hydrodenitrogenation, and hydrodesulfurization, producing hydrocarbon fuels.
- Catalytic hydrothermal gasification of the aqueous byproduct stream effectively produced fuel gas and allowed for
Water as a solvent in microwave assisted organic synthesisPrashantChavan93
Prashant Chavan
Reserach Scholar
M.S.(Pharm) in Medicinal Chemistry
National Institute of Pharmaceutical Education and Research Mohali, Punjab (India) 160062
mcm20_prashant@niper.ac.in
This document discusses a study on the hydrothermal conversion of pentoses like xylose and arabinose to furfural with simultaneous extraction of furfural using supercritical carbon dioxide (SC-CO2). The maximum furfural yield from xylose was 68% at 230°C and 12 MPa. Kinetic data on the conversion of arabinose to furfural was also provided, showing similarities to xylose conversion. Furfural yields from biomass hydrolysates were lower than from pure sugars due to side reactions. Simultaneous SC-CO2 extraction significantly increased furfural extraction yields in all cases. The processing route could be integrated into biorefinery concepts utilizing water and CO2 as
1) The document describes a study that investigates the esterification of palm fatty acid distillate (PFAD) using a heterogeneous sulfonated microcrystalline cellulose catalyst and compares it to using sulfuric acid as the catalyst.
2) The solid catalyst was characterized and tested under various conditions of catalyst loading, temperature, and fatty acid to methanol ratio. Sulfuric acid performed better but the solid catalyst allows for easier recovery and reusability.
3) The kinetics of the esterification reaction were analyzed considering the biphasic liquid-liquid nature of the system that forms, with the two phases reaching equilibrium, in both catalyst systems.
The document discusses using the solvent N-methylmorpholine-N-oxide (NMMO) to dissolve cellulose for enzymatic hydrolysis. Key findings include:
1) Enzymatic hydrolysis rates were higher for cellulose dissolved in NMMO compared to regenerated cellulose. This supports conducting pretreatment and hydrolysis in a single step.
2) Among ionic liquids tested, enzymatic activity was highest in NMMO and gradually decreased in two other ionic liquids.
3) Preliminary experiments in a twin screw reactor demonstrated the potential to process high cellulose loads and achieve higher sugar yields in a continuous process.
Isolation and Screening of Hydrogen Producing Bacterial Strain from Sugarcane...Editor IJCATR
The aim of this study is to isolate a highly competent bacterium with potent cellulose degrading capability and a better
hydrogen producer. Soil sample from sugarcane bagasse yard was isolated, serially diluted and plated on cellulose specific nutrient
agar plate. Four colonies have been isolated in which a single colony has potent cellulose degrading ability and the highest hydrogen
productivity of 275.13 mL H2 L-1. The newly isolated bacterium was morphologically and biochemically characterized. The
molecular characterization of the bacterium was carried out using 16S rDNA sequencing and the organism was identified as
Bacilllus subtilis AuChE413. Proteomic analysis such as MALDI-TOF was carried out to differentiate the isolated Bacillus subtilis
from Bacillus thuringiensis and Bacillus amyloliquefaciens. Phylogenetic tree was constructed to analyze the evolutionary
relationship among different genus and species with the newly isolated strain.
1) Self-assembled monolayer coated gold nanoparticles catalyze the aerobic oxidation of alpha-hydroxy ketones to aryl 1,2-diketones in water.
2) This provides an efficient one-pot synthesis of quinoxaline derivatives by in situ oxidation of alpha-hydroxy ketones and subsequent condensation with aryl 1,2-diamines in water.
3) 4-Aminothiophenol self-assembled monolayer coated gold nanoparticles were found to be an effective catalyst for these reactions, providing good to excellent yields of products under mild conditions in water.
1) A one-pot synthesis of novel 9-aminoacridine derivatives is described using simple nucleophilic aromatic substitution and addition-elimination reactions with readily available starting materials.
2) Two general reaction conditions are established - refluxing in ethanol overnight or using cesium carbonate in DMF at 90°C for 12 hours. These methods give moderate to good yields of various substituted 9-aminoacridine derivatives.
3) Specifically, 9-(azaarylamino)acridines are synthesized from chloropyridines and chloropyrimidines via SNAr reactions. 9-(Acridinylamino)quinones are also synthesized from haloquinones and halo naphtho
This document discusses hydrogen delivery through liquid organic hydrides (LOH) such as cycloalkanes. It covers considerations for this potential technology, including dehydrogenation catalysts, catalyst supports, and reaction kinetics and thermodynamics. Key points include: (1) Cycloalkanes such as cyclohexane and methylcyclohexane can store 6-8% hydrogen by weight and are liquid at ambient conditions, making them suitable for hydrogen transport. (2) Dehydrogenation over metal catalysts such as Pt is an effective way to release hydrogen from the hydrides. (3) Pt-based catalysts generally have the highest activity and selectivity, while bi-metallic catalysts may have even higher activity through synergistic effects
This document summarizes research on developing an orthogonal fatty acid biosynthesis system in E. coli for oleochemical production. Key findings include:
- Several type I fatty acid synthase (FAS) enzymes from Corynebacterium glutamicum and Mycobacterium tuberculosis were cloned and expressed solubly in E. coli.
- The activity of several type I FAS enzymes was demonstrated in vivo, and C. glutamicum FAS was used to produce fatty alcohols and methyl ketones.
- This represents the first example of a heterologous FAS pathway in E. coli and lays the groundwork for further optimizing renewable oleochemical production.
This study evaluated the biodegradability of the antioxidant diaryl-p-phenylene diamine (DAPD) using a modified inherent biodegradation test. DAPD is used in tires and rubber products. Previous studies found it was not readily biodegradable using standard tests. This study used radiolabeled DAPD (R-898) at low concentrations of 10-100 μg/L added to silica gel to enhance solubility, along with a surfactant. After 28 days, no parent compound remained. After 63 days, 37% had mineralized and 29% was incorporated into biomass, demonstrating biodegradation. The modifications enhanced the sensitivity of the test to show DAPD
This document describes research on the heterologous expression of an NADP-dependent [NiFe]-hydrogenase from Pyrococcus furiosus in Escherichia coli. The researchers were able to successfully produce a functional form of the recombinant hydrogenase enzyme by co-expressing 13 P. furiosus genes involved in hydrogenase maturation in E. coli. Remarkably, providing only the four structural genes encoding the hydrogenase subunits and a single protease from P. furiosus was sufficient for the native E. coli maturation machinery to generate functional hydrogenase. This demonstrates that E. coli can assemble a functional hydrogenase from a phylogenetically distant hyperthermophilic organism.
Liquid crystal bio-based epoxy coating with enhanced performanceIJERA Editor
Tetrafunctional rosin based epoxy was synthesized and cured with either rosin based hardener or conventional
phenylene diamine to study the feasibility of producing high performance thermosetting polymer from
renewable resource. The chemical structure of the prepared epoxy was confirmed by elemental analysis, FTIR,
1HNMR, UV, total acid number and epoxy equivalent weight. Dynamic mechanical (DMA) and
thermogravimetric (TGA) analyses results indicate that fully biobased epoxy system possesses high glass
transition temperature (Tg), high modulus (G`) and improved thermal stability.
1) An efficient protocol has been developed for the synthesis of biaryls via Pd/Cu catalyzed coupling of phenylhydrazines in water without using any ligands.
2) Both Pd and Cu catalysts were found to be essential for the reaction, with Pd(TFA)2 and Cu(OAc) providing the best results.
3) A range of substituted phenylhydrazines underwent homo- and cross-coupling reactions under the optimized conditions to provide the biaryl products in good to excellent yields.
This document discusses an integrated acetic acid based one-pot ethanolamine acetate pretreatment process for efficient depolymerization of poplar polysaccharides. Key points:
(1) The new process simultaneously removes 88% of hemicellulose and extracts up to 46% of lignin from poplar biomass.
(2) It yields over 80% enzyme-hydrolyzed glucose, attributed to increased accessible surface area of cellulose.
(3) Analysis indicates the ionic liquid component is a good lignin solvent, leading to higher delignification.
Overall, integrating ionic liquid with acid pretreatment is a promising strategy for effective pretreatment of woody lignocellulose.
Highly stable pt ru nanoparticles supported on three-dimensional cubic ordere...suresh899
The cost of the catalysts used in the direct methanol fuel cell
poses a challenge to its widespread use as an energy efficient and environment
friendly fuel conversion technology. In this study, two types of highly ordered
mesoporous carbon CMK-8 (I and II) with high surface area and 3-D
bicontinuous interpenetrating channels were synthesized and deposited with
PtRu nanoparticles using the sodium borohydride reduction method. The
electrocatalytic capabilities for methanol oxidation were investigated using
cyclic voltammetry and chronoamperometry, and the results were compared
with that of PtRu deposited on Vulcan XC-72 using the same preparation
method as well as with commercial PtRu/C (E-TEK) catalyst. Pt Ru/CMK-8-I synthesized by the method developed in this work revealed an
outstanding specific mass activity (487.9 mA/mg) and superior stability
compared with the other supports, thus substantiating its potential to reduce
the costs of DMFC catalysts.
This document summarizes a student research project analyzing the dose response of cellulase enzyme cocktails under variable temperature, pH, and ionic liquid conditions. The student determined the optimal temperatures and pH levels for different enzymes to catalyze glucose production from cellulose. Initial experiments found optimal temperatures of 65°C and 85°C for enzymes Cel_9A and Cel_5A, respectively. Further experiments analyzed the effects of varying temperature, pH, and ionic liquid concentration on glucose production across different enzyme doses. The goal was to optimize conditions to maximize glucose yields for producing biofuels through fermentation.
Steam pretreatment and acid-catalyzed pretreatment technologies are widely used to make lignocellulose more accessible to enzymatic hydrolysis. During these pretreatments, hemicellulose is partially removed and lignin is redistributed, increasing the surface area and pore volume of the material. This exposes the cellulose microfibrils and makes them more accessible to cellulase enzymes. Still, some technical challenges around maximizing sugar yields and reducing costs remain to be solved before these pretreatment technologies can be commercially viable at large scale.
This document summarizes a study on the hydrothermal dissolution of willow biomass in hot compressed water. The key findings are:
1) A 95% dissolution of willow was achieved at temperatures as low as 200°C and pressures of 10 MPa, with lignin and hemicellulose dissolving first, followed by cellulose between 280-320°C.
2) A proposed dissolution mechanism involves the rapid fragmentation and hydrolysis of lignin, hemicellulose, and cellulose into oligomers and other water-soluble products like glucose.
3) A continuous flow process was found to be more effective for dissolution than a batch process, due to reduced recondensation of dissolved oligomers.
cellulose, the most abundant natural biopolymer, has long been
investigated as a new green source to replace non-renewable materials and chemicals, but its highly ordered hydrogen bond network
and high crystallinity, which both detract cellulose reactivity and
solubility (Kondo, 1998), have made it difficult to exploit the full
potential of cellulose materials. To overcome these problems, many
new solvent systems have been studied to enable the homogeneous
modification of cellulose (Ramos, Frollini, & Heinze, 2005; Wu
et al., 2004). Many modifications are nevertheless still preferably
conducted heterogeneously in an aqueous medium, particularly
because of the advantages of this approach with regard to toxicity,
volatility and price.
One potential react
The document presents a kinetic model for the acid-catalyzed delignification of sugarcane bagasse by aqueous acetic acid (AcH). The model introduces the concept of "potential degree of delignification (dD)" to account for the multilayered structure of plant cell walls and the inhibitory effect of dissolved lignin. Experimental results showed that delignification rate followed first-order kinetics with respect to sulfuric acid concentration but had a high reaction order with respect to AcH concentration. The activation energy for delignification was determined to be 64.41 kJ/mol. Mechanism analysis found that cleavage of α-aryl ether bonds in lignin was mainly responsible for lignin fragment formation, and increasing AcH
This document discusses improving the bioenergy conversion efficiency of food waste through pretreatment, co-digestion, and reactor type selection. Food waste has great potential for methane production through anaerobic digestion but currently suffers from low conversion efficiency due to its long hydraulic retention time, low organic loading rate, and low conversion rate. Pretreatment technologies like enzymatic pretreatment and co-digestion with other wastes can help accelerate hydrolysis of organic solids and enhance methane production. Using a third generation anaerobic reactor along with enzymatic pretreatment and co-digestion of food waste with landfill leachate may allow over 90% of organic matter in food waste to be recovered as bioenergy with an organic loading rate greater
This document summarizes research on the hydrothermal liquefaction of algae feedstocks in a continuous-flow reactor system. Key points:
- Algae can be converted to an upgradeable biocrude through hydrothermal liquefaction at 350°C and 20 MPa in a continuous-flow reactor, without the need for solvents. High carbon conversions were achieved even at high algae concentrations.
- Catalytic hydrotreating was effectively used to upgrade the biocrude through hydrodeoxygenation, hydrodenitrogenation, and hydrodesulfurization, producing hydrocarbon fuels.
- Catalytic hydrothermal gasification of the aqueous byproduct stream effectively produced fuel gas and allowed for
Water as a solvent in microwave assisted organic synthesisPrashantChavan93
Prashant Chavan
Reserach Scholar
M.S.(Pharm) in Medicinal Chemistry
National Institute of Pharmaceutical Education and Research Mohali, Punjab (India) 160062
mcm20_prashant@niper.ac.in
This document discusses a study on the hydrothermal conversion of pentoses like xylose and arabinose to furfural with simultaneous extraction of furfural using supercritical carbon dioxide (SC-CO2). The maximum furfural yield from xylose was 68% at 230°C and 12 MPa. Kinetic data on the conversion of arabinose to furfural was also provided, showing similarities to xylose conversion. Furfural yields from biomass hydrolysates were lower than from pure sugars due to side reactions. Simultaneous SC-CO2 extraction significantly increased furfural extraction yields in all cases. The processing route could be integrated into biorefinery concepts utilizing water and CO2 as
1) The document describes a study that investigates the esterification of palm fatty acid distillate (PFAD) using a heterogeneous sulfonated microcrystalline cellulose catalyst and compares it to using sulfuric acid as the catalyst.
2) The solid catalyst was characterized and tested under various conditions of catalyst loading, temperature, and fatty acid to methanol ratio. Sulfuric acid performed better but the solid catalyst allows for easier recovery and reusability.
3) The kinetics of the esterification reaction were analyzed considering the biphasic liquid-liquid nature of the system that forms, with the two phases reaching equilibrium, in both catalyst systems.
The document discusses using the solvent N-methylmorpholine-N-oxide (NMMO) to dissolve cellulose for enzymatic hydrolysis. Key findings include:
1) Enzymatic hydrolysis rates were higher for cellulose dissolved in NMMO compared to regenerated cellulose. This supports conducting pretreatment and hydrolysis in a single step.
2) Among ionic liquids tested, enzymatic activity was highest in NMMO and gradually decreased in two other ionic liquids.
3) Preliminary experiments in a twin screw reactor demonstrated the potential to process high cellulose loads and achieve higher sugar yields in a continuous process.
Isolation and Screening of Hydrogen Producing Bacterial Strain from Sugarcane...Editor IJCATR
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hydrogen producer. Soil sample from sugarcane bagasse yard was isolated, serially diluted and plated on cellulose specific nutrient
agar plate. Four colonies have been isolated in which a single colony has potent cellulose degrading ability and the highest hydrogen
productivity of 275.13 mL H2 L-1. The newly isolated bacterium was morphologically and biochemically characterized. The
molecular characterization of the bacterium was carried out using 16S rDNA sequencing and the organism was identified as
Bacilllus subtilis AuChE413. Proteomic analysis such as MALDI-TOF was carried out to differentiate the isolated Bacillus subtilis
from Bacillus thuringiensis and Bacillus amyloliquefaciens. Phylogenetic tree was constructed to analyze the evolutionary
relationship among different genus and species with the newly isolated strain.
Oleaginous fungal lipid fermentation on combined acid and alkali-pretreated ...zhenhua82
A combined hydrolysis process, which first mixed dilute acid- and alkali-pretreated corn stover at a 1:1 (w/w) ratio, directly followed by enzymatic saccharification without pH adjustment, has been developed in this study in order to minimize the need of neutralization, detoxification, and washing during the process of lignocellulosic biofuel production. The oleaginous fungus Mortierella isabellina was selected and applied to the combined hydrolysate as well as a synthetic medium to compare fungal lipid accumulation and biodiesel production in both shake flask and 7.5 L fermentor. Fungal cultivation on combined hydrolysate exhibited comparable cell mass and lipid yield with those from synthetic medium, indicating that the integration of combined hydrolysis with oleaginous fungal lipid fermentation has great potential to improve performance of advanced lignocellulosic biofuel production
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Poultry Manure (PM) produced in Egypt in huge amount and considered as an environmental problem. Poultry waste can, however, be fermented anaerobically to produce biogas, but its great majority of nitrogen that affects the efficiency and methane ratio of generated biogas. So, the aim of this work to enhance the methane ratio in biogas produced from Poultry Manure using the Dried Bread (DB). 100:0, 25:75, 50:50, 75:25 and 0:100% ratios of DB:PM mixtures has been studied. Biogas yield, C/N ratio, pH, and methane content were studied. The initial pH was 6.43±0.01, 6.85+0.31 6.87±0.56, 6.89±0.23, and 6.95±0.35 respectively; and finally, it was 7.9±0.50, 8.20±0.03, 8.51±0.34, 8.64±0.21 and 8.86+0.25 respectively. While the produced biogas from 100 gm from each mixture was 1180, 1050, 943, 890 and 785 mL respectively with regression coefficient = 0.983. From the obtained results the biogas with high methane content (56%) was produced from mixture of 3:1 DB: PM. The study conclude that Dried Bread can be used to enhance the properties of poultry manure for best biogas quality.)
This document describes a project to design an energy-producing waste treatment system using anaerobic co-digestion of organic wastes from the University of Arkansas Swine and Poultry Units coupled with algae cultivation. A prototype was constructed and tested to generate data for designing a full-scale system. The full-scale system was designed to treat all biological wastes from the units while producing net energy and retaining nutrients that could be used as fertilizer.
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This document summarizes a student's project to produce bioethanol from waste paper through acid hydrolysis, fermentation, and distillation. The student measured various physico-chemical properties of the produced bioethanol, including viscosity, density, boiling point, and specific gravity, and compared the results to literature standards. Overall, the student was able to successfully produce bioethanol from waste paper and determined that the conversion and fermentation processes were effective, though the yields and some properties differed from literature values potentially due to feedstock characteristics and production technology used.
This document summarizes a study that explored using an aqueous two-phase system (ATPS) composed of polyethylene glycol (PEG) and sodium citrate to purify lectin from Canavalia grandiflora seeds. A 24 full factorial design was used to study how four factors (PEG molar mass, PEG concentration, pH, and citrate concentration) affected the partitioning of the lectin ConGF. The results showed that ConGF preferentially partitioned to the PEG-rich top phase. A system of 20% PEG 400 and 20% citrate at pH 6 allowed recovery of ConGF with an 8.67 partitioning coefficient and 104% yield, demonstrating the efficiency of this ATPS for pur
Partition of lectin from canavalia grandiflora benth in aqueous two phase
201403045_ftp
1. Co-solvent Pretreatment Reduces Costly Enzyme
Requirements for High Sugar and Ethanol Yields from
Lignocellulosic Biomass
Thanh Yen Nguyen,[a, b]
Charles M. Cai,[a, c, d]
Rajeev Kumar,[a, d]
and Charles E. Wyman*[a, b, c, d]
Introduction
Lignocellulosic biomass, in the form of agricultural, herba-
ceous, and woody residues and energy crops, promises to pro-
vide a sufficient sustainable resource to address global energy
demands and reduce dependence on petroleum-based liquid
fuels.[1]
Its low cost is also attractive with lignocellulosic bio-
mass at $60drytonÀ1
, which is equivalent in unit energy cost
to oil at approximately $20barrelÀ1
.[2]
Natural gas production
from fossil resources can serve to reduce petroleum consump-
tion in the near future, however, it is a finite resource, and its
consumption contributes to overall atmospheric greenhouse
gas (GHG) emissions. In contrast, bioenergy from lignocellulo-
sic biomass is sustainable in the long term, and the GHGs pro-
duced from burning biofuels originate from atmospheric CO2
sequestered by photosynthesis and are reabsorbed by growing
new plants to replace those harvested. In light of this, realistic
and scalable technologies are particularly needed to capture
the energy in lignocellulosic biomass as aromatic, hydrocarbon,
and alcohol transportation fuels because the transportation
sector currently consumes approximately two-thirds of the
world’s petroleum production.[3]
Lignocellulosic biomass is composed of hemicellulose, cellu-
lose, and lignin in a heterogeneous matrix that is recalcitrant;
it is structurally durable and resistant to microbial or enzymatic
breakdown.[4]
This recalcitrance is the major economic obstacle
to the conversion of biomass to sugars or other reactive inter-
mediates with high yields at low enough costs for widespread
use.[1a,3b]
Biomass pretreatment is essential to overcome the re-
calcitrance of most biomass materials to downstream biologi-
cal and chemical processes. Chemical and physical pretreat-
ment methods include heat, acid, and/or chemicals, usually in
aqueous-based reactions.[4a,5]
In these two-stage operations,
thermochemical pretreatment (Stage 1) opens up the biomass
structure for subsequent enzymatic saccharification (Stage 2)
by a mixture of enzymes (“cocktails”) that release sugars from
the pretreated solids.[5a,6]
Although modern saccharification en-
zymes are highly stable and selective, their effectiveness is
largely influenced by the efficacy of the pretreatment stage in
which 1) incomplete removal/relocation of hemicellulose and/
or lignin impedes enzyme function, which necessitates higher
enzyme loadings that increase costs significantly, and 2) inef-
fective alteration of the polysaccharides that remain in the
solids from pretreatment can reduce enzyme access to binding
sites, which limits potential sugar yields.[7]
Thus, it is desirable
We introduce a new pretreatment called co-solvent-enhanced
lignocellulosic fractionation (CELF) to reduce enzyme costs dra-
matically for high sugar yields from hemicellulose and cellu-
lose, which is essential for the low-cost conversion of biomass
to fuels. CELF employs THF miscible with aqueous dilute acid
to obtain up to 95% theoretical yield of glucose, xylose, and
arabinose from corn stover even if coupled with enzymatic hy-
drolysis at only 2 mgenzyme gglucan
À1
. The unusually high sacchari-
fication with such low enzyme loadings can be attributed to
a very high lignin removal, which is supported by composition-
al analysis, fractal kinetic modeling, and SEM imaging. Subse-
quently, nearly pure lignin product can be precipitated by the
evaporation of volatile THF for recovery and recycling. Simulta-
neous saccharification and fermentation of CELF-pretreated
solids with low enzyme loadings and Saccharomyces cerevisiae
produced twice as much ethanol as that from dilute-acid-pre-
treated solids if both were optimized for corn stover.
[a] T. Y. Nguyen,+
Dr. C. M. Cai,+
Dr. R. Kumar, Prof. C. E. Wyman
Center for Environmental Research and Technology (CE-CERT)
Bourns College of Engineering
University of California
Riverside, 1084 Columbia Avenue, Riverside, California 92507 (USA)
Fax: (+1)951-781-5790
E-mail: cewyman@engr.ucr.edu
[b] T. Y. Nguyen,+
Prof. C. E. Wyman
Department of Bioengineering
Bourns College of Engineering
University of California
Riverside, 217 Materials Science & Engineering
900 University Ave., Riverside, CA 92507 (USA)
[c] Dr. C. M. Cai,+
Prof. C. E. Wyman
Department of Chemical and Environmental Engineering
Bourns College of Engineering
University of California
Riverside, 446 Winston Chung Hall
900 University Ave., Riverside, CA 92507 (United States)
[d] Dr. C. M. Cai,+
Dr. R. Kumar, Prof. C. E. Wyman
BioEnergy Science Center (BESC)
Oak Ridge National Laboratory (ORNL)
Oak Ridge, TN (USA)
[+
] These authors contributed equally to this work.
Supporting Information for this article is available on the WWW under
http://dx.doi.org/10.1002/cssc.201403045.
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Full PapersDOI: 10.1002/cssc.201403045
2. for an effective pretreatment to remove hemicellulose and
lignin to improve the accessibility of the pretreated solids to
enzymes so that high total sugar yields from both hemicellu-
lose and cellulose can be achieved with low enzyme load-
ings.[7a,8]
Currently, leading pretreatment strategies that are attractive
for commercial use include, but are not limited to, processes
based on hydrothermal, dilute acid (DA), solvent (such as etha-
nol-organosolv or cellulose solvent and organic solvent based
lignocellulose fractionation; COSLIF), ammonia (ammonia fiber
expansion (AFEX), ammonia recycled percolation (ARP), and
soaking in aqueous ammonia), and alkali treatment.[6,9]
Although each approach has its advantages, incremental imple-
mentation costs must be compensated by significant improve-
ments in total sugar recovery and the ability to achieve high
yields of fuels in downstream bioconversion processes at low
enzyme loadings. We present here a new solvent-based pre-
treatment strategy called co-solvent-enhanced lignocellulosic
fractionation (CELF) that employs aqueous THF solutions to en-
hance DA pretreatment significantly. DA pretreatment is a re-
search and commercial pretreatment benchmark[10]
as evi-
denced by its wide adoption for pretreatment-related research
and choice for techno-economic analyses by the National Re-
newable Energy Laboratory (NREL)[11]
as a relatively low-cost and
effective pretreatment for corn stover and other feedstocks.[12]
CELF employs THF because it is a unique polar aprotic sol-
vent that is miscible with water over a wide range of condi-
tions and concentrations and has the added benefit that it can
be produced sustainably from biomass.[13]
In its miscible
regime at high reaction severities, we showed previously that
the reaction of lignocellulosic biomass with acidified aqueous
THF solutions caused extensive lignin removal from biomass
solids and catalyzed the solubilization of cellulose and hemicel-
lulose to enhance the overall sugar dehydration product yields
(furfural, 5-hydroxymethylfurfural, and levulinic acid) that could
be used as fuel precursors for catalytic reactions.[13,14]
These re-
sults prompted us to hypothesize that less severe reaction
conditions would solubilize most of the hemicellulose sugars
with limited breakdown to dehydration products and remove
most of the lignin to produce cellulose-rich solids that would
lend themselves to nearly complete sugar release at low
enzyme loadings. Thus, the study reported here was undertak-
en to optimize CELF as a pretreatment of corn stover as
a model biomass feedstock, directly compare the resulting per-
formance with that by DA pretreatment to define the unique
advantages of CELF, and demonstrate its integration with si-
multaneous saccharification and fermentation (SSF) to produce
valuable fuels and chemicals.
Results and Discussion
Optimization of corn stover pretreatment to maximize over-
all total sugar yields
This study focused on the fate of glucose, xylose, and arabi-
nose during CELF and DA pretreatments in light of their domi-
nance in corn stover composition. To present a fair compari-
son, we first optimized reaction conditions to achieve the high-
est total sugar yields (glucose, xylose, and arabinose) from
CELF or DA pretreatment of corn stover (Stage 1) combined
with subsequent enzymatic hydrolysis of the pretreated solids
(Stage 2). Dilute sulfuric acid (0.5 wt%) was used for both CELF
and DA pretreatments as it is an inexpensive strong acid that
can be neutralized easily at dilute concentrations and is often
the acid of choice. We selected a 1:1 THF/water volume mix-
ture for all CELF reactions as it was found previously to be the
lowest solvent concentration required for effective delignifica-
tion of lignocellulosic biomass.[13]
Although higher solvent
ratios up to 7:1 can further improve biomass solubilization, the
formation of unwanted sugar dehydration products is also in-
creased. For CELF, the lowest optimal reaction temperature of
1508C was chosen to remain outside the known miscibility
gap for THF/water mixtures between 71.8 and 137.18C.[15]
Short heat-up (4 min) and cool-down (1 min) times ensure
that the reactants spend little time passing through the immis-
cible region to minimize the possibility of some impact on re-
action kinetics. For optimization, Stage 2 enzymatic hydrolysis
of pretreated corn stover solids was performed with the Accel-
lerase 1500 enzyme cocktail (cellulase+b-glucosidase) at an
enzyme loading of 15 mgenzyme gglucan
À1
to yield glucose mono-
mers. Enzyme loadings were based on the glucan composition
of the corn stover before pretreatment for a fair comparison
between the two pretreatments.[5a]
The total sugar yields from combined pretreatment and en-
zymatic hydrolysis were determined over a range of pretreat-
ment times to find the optimal reaction time for the CELF pre-
treatment of corn stover (Figure 1). Most of the xylose and ara-
binose was released in Stage 1, whereas the majority of the
glucose was obtained in Stage 2, consistent with the typical
production of sugars from DA pretreatment. However, in con-
trast to DA pretreatment trends in which Stage 2 glucose
yields tend to increase continually with pretreatment time,
Stage 2 glucose yields from the enzymatic hydrolysis of CELF-
pretreated corn stover remained relatively constant over
a range of pretreatment times (Figure 1A). As little degradation
of glucose occurred under the CELF pretreatment conditions
applied and enzymatic hydrolysis was effective over a wide
range of pretreatment times, the total glucose yield from both
stages was nearly 100% of the theoretical maximum that par-
alleled the trend for Stage 2. However, the Stage 1 xylose yield
for CELF peaked at 89% for an approximately 25 min pretreat-
ment, and further reaction reduced xylose yields as a result of
degradation. As most of the xylose was released in Stage 1
and most of the xylose that remained in the pretreated solids
was released in subsequent enzymatic hydrolysis, the total
xylose yield paralleled the trend for Stage 1. Arabinose yields
were fairly constant at approximately 80% of the theoretical
yield over the course of the reaction times. As a result of these
trends, the optimal reaction time of 25 min for the total com-
bined sugars yield from CELF pretreatment shown in Figure 1C
was largely dictated by the xylose yield from Stage 1 (Fig-
ure 1B). This outcome suggested that CELF pretreatment of
corn stover could be optimized simply based on xylose recov-
ery in the liquid hydrolyzate from pretreatment.
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Full Papers
3. The optimal reaction conditions developed in this study for
DA pretreatment of corn stover without THF were consistent
with those established by previous work:[16]
a 20 min reaction
at 1608C with 0.5 wt% sulfuric acid. Maximization of the total
sugar yields from combined pretreatment and enzymatic hy-
drolysis required tradeoffs as sugar yields from enzymatic hy-
drolysis increased continually with pretreatment time and
xylose yields from pretreatment peaked well before the maxi-
mum glucose yield was obtained. This contrasts with CELF pre-
treatment in which xylose was not sacrificed in Stage 1 to real-
ize high enough yields in Stage 2 to achieve the highest possi-
ble overall total sugar yields.[16]
The compositions of solids from both DA and CELF pretreat-
ments of corn stover under the optimal conditions for the
highest overall total sugar yields are shown in Figure 2 based
on 100 g of initial raw corn stover before pretreatment. These
results show that although the fates of glucan and arabinan
were similar for both pretreatments, CELF pretreatment im-
proved the removal of xylan and lignin dramatically compared
to DA pretreatment. The remaining component masses are
1.3 g xylan and 3.4 g lignin for the CELF-pretreated solids com-
pared to 2.9 g xylan and 15.0 g lignin for the DA-pretreated
solids based on 100 g of initial corn stover (Figure 2). The re-
duced solid mass from CELF pretreatment was largely because
of extensive delignification, which is not possible with DA pre-
treatment, higher solubilization of other components such as
ash, proteins, and extractives, and less pseudolignin formation
caused by sugar degradation that may actually increase the
measured K-lignin content in pretreated solids from the DA
pretreatment.[17]
As observed previously with maple wood,[13]
THF is highly effective in the delignification of biomass and in
this case produces a much more glucan-enriched material than
that from DA pretreatment (75 vs. 52 wt% glucan, respective-
ly). However, the total mass of glucan that remained in the
solids was comparable after DA and CELF pretreatments de-
spite a 108C reduction in temperature with CELF under opti-
mal reaction conditions, which supports our early observation
that THF can catalyze the hydrolysis of biomass sugars.[13]
Effect of reduced enzyme loadings on total sugar yields
As enzymes contribute approximately 20% of the total cost of
the production of fermentable carbohydrates from lignocellu-
losic biomass,[3b]
one of the most important challenges in the
development of effective pretreatment technologies is the re-
duction of the enzyme requirement for high sugar yields. En-
zymes have been estimated to cost up to $1.47gallonethanol
À1
based on typical yields and conversions (%70%) for ethanol
production from corn stover based on a benchmark DA pre-
treatment at a moderate loading of 20 mgenzyme gglucan
À1
.[18]
Thus, as an example, the reduction of the enzyme loading by
a factor of four could lower enzyme costs significantly to
a more economical value of $0.37gallonethanol
À1
. The results of
the Stage 2 enzymatic hydrolysis of solids produced from opti-
mized DA and CELF pretreatments of corn stover for loadings
of 30, 15, 5, and 2 mgenzyme gglucan
À1
based on the raw glucan
composition are shown in Figure 3. These results show that
CELF pretreatment (Figure 3B) achieved higher total sugar
yields at all enzyme loadings compared to DA pretreatment
Figure 1. Optimization of pretreatment times for the CELF pretreatment of corn stover to maximize total sugar (glucose, xylose, and arabinose) yields from
combined pretreatment (Stage 1) and enzymatic hydrolysis (Stage 2): A) glucose yields, B) xylose yields, and C) total combined glucose+xylose+arabinose
yields. Reaction conditions: 5 wt% corn stover, 1508C, 0.5% H2SO4, and 1:1 THF/water volume ratio. Stage 2 was performed using a 15 mgprotein gglucan
À1
load-
ing of Accellerase 1500 enzyme based on glucan in corn stover before pretreatment.
Figure 2. Tracking the mass of glucan, xylan, arabinan, lignin, and other
compounds left in the solids produced by DA and CELF pretreatments at
conditions optimized for the recovery of the highest total overall sugar
yields. The values shown for DA and CELF are based on the content of each
component in 100 g of corn stover before pretreatment. Reaction condi-
tions: DA: 1608C, 0.5% H2SO4, 20 min; CELF: 1508C, 0.5% H2SO4, 25 min, 1:1
THF/water volume ratio.
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Full Papers
4. (Figure 3A). Additionally, the CELF-pretreated material realized
nearly theoretical yields of glucose even at low loadings of 2
and 5 mgenzyme gglucan
À1
, albeit at longer incubation times (16
and 5 days, respectively). These profiles are in stark contrast to
those for DA-pretreated corn stover solids that had lower rates
of glucan release and incomplete hydrolysis at loadings of
15 mgenzyme gglucan
À1
or less, likely caused by cellulose surface
blockage by lignin and pseudolignin and/or enzyme inhibition/
adsorption by lignin and/or pseudolignin.[17a,19]
The glucose
yield profiles versus enzymatic hydrolysis incubation time also
show that long-term glucose yields for solids from DA pretreat-
ment decreased with each successively lower enzyme loading,
whereas long-term yields reached nearly 100% for the CELF-
pretreated material, although it required longer reaction times.
Thus, CELF pretreatment reduced the recalcitrance of corn
stover to such an extent that a 10-fold reduction in enzyme
loading still achieved very high yields and could translate into
a decrease of the enzyme cost to $0.15gallonethanol
À1
, a saving
of over $1.00gallonethanol
À1
. Future techno-economic analysis is
needed to evaluate the cost of implementing CELF pretreat-
ment compared to DA pretreatment to demonstrate overall
cost savings. As described later, the extent of THF recovery
would be crucial to plant economics.
The total combined sugar yields at loadings of 2, 5, and
15 mgenzyme gglucan
À1
for solids from CELF and DA pretreatments
under optimized pretreatment conditions expressed as the
sum of glucose, xylose, and arabinose masses obtained from
Stage 1+Stage 2 divided by the initial total mass of these
three sugars and normalized based on 100 g total sugars in
the initial material before pretreatment are shown in Figure 4.
Although the xylose (34–36%) and arabinose yields (5%) were
comparable for both CELF and DA pretreatments as a result of
the similar sugar release in Stage 1, total combined sugar
yields were higher for CELF pretreatment than for DA pretreat-
ment at all enzyme loadings because of the higher glucose re-
lease in Stage 2 from the CELF-pretreated solid. Notably, the
overall sugar yields from CELF-pretreated solids reached ap-
proximately 95% even at the low enzyme loading of
2 mgenzyme gglucan
À1
, although it took 14 days to reach this level,
whereas yields from DA-pretreated solids were only approxi-
mately 70% after 14 days at this low enzyme loading. The ap-
parent rate of glucose release was also higher from CELF-pre-
treated solids, as illustrated by the recovery of over 95% of the
total potential sugar in corn stover in only two days following
CELF pretreatment compared to the 14 days needed for the
DA-pretreated material to achieve an 85% total sugar yield at
a loading of 15 mgenzyme gglucan
À1
. Even at the longer incubation
times for the latter, the lower total combined sugar yields were
mostly attributable to incomplete glucan hydrolysis in Stage 2,
as xylose and arabinose recovery was comparable to that from
CELF pretreatment. A mass balance that illustrates the fate of
each sugar is shown in Supporting Information Figure S1).
Figure 3. Comparison of glucose yields from the enzymatic hydrolysis of
solids from optimized A) DA and B) CELF pretreatments of corn stover
versus enzymatic hydrolysis time over a range of Accellerase 1500 enzyme
loadings from 2–30 mgenzyme gglucan
À1
. Pretreatment reaction conditions were
those that gave the highest total combined sugar yields at a loading of
15 mgenzyme gglucan
À1
: DA: 1608C, 0.5% H2SO4, 20 min; CELF: 1508C, 0.5%
H2SO4, 25 min, 1:1 THF/water volume ratio.
Figure 4. Overall Stage 1+Stage 2 yields of glucose, xylose, and arabinose
from CELF- and DA-pretreated corn stover solids based on 100 g of total
monomeric equivalent of the glucan, xylan, and arabinan content in untreat-
ed corn stover. The Stage 2 incubation time in days is shown at the top of
each bar, e.g., D14 represents 14 days. 100% corresponds to the maximum
amount of sugars that could be realized from the total glucan, xylan, and
arabinan in corn stover.
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5. Insights gained by a fractal model of enzymatic hydrolysis
kinetics
A fractal kinetic model based on an empirical curve fitted to
the enzymatic hydrolysis results presented provided additional
insights into the cause of the sugar-yield plateau suffered by
DA-pretreated corn stover compared to the highly reactive ma-
terial produced by CELF (fractal model and experimental fit pa-
rameters are given in Table S1 and Figure S2, respectively). The
fractal model used is based on classical first-order kinetics but
replaces the rate constant k with a transient rate coefficient
kt =ktÀh
that decays over time with a fractal exponent h. The
values of the transient rate parameter kt can be interpreted in
terms of both substrate features and enzyme loadings to sug-
gest mechanistic differences in the enzymatic hydrolysis of
CELF- and DA-pretreated solids. If kt is plotted against the
glucan conversion (Figure 5A), differences in the enzyme–sub-
strate interactions can be seen. Specifically, in the higher
glucan conversion regime of 60–100% in which the accessible
substrate surface area was reduced significantly, CELF-pretreat-
ed corn stover exhibited higher kt values that decreased more
slowly with increasing conversion from 0.039–0.030 hÀ1
(Fig-
ure 5A) at the lower loading of 5 mgenzyme gglucan
À1
, compared to
the larger decrease for DA-pretreated corn stover at higher
loadings from 0.019–0.006 hÀ1
for 15 mgenzyme gglucan
À1
and
0.027–0.007 hÀ1
for 30 mgenzyme gglucan
À1
. This large difference
suggests that CELF pretreatment produces substrates that sus-
tain a greater accessibility to enzymes over the course of hy-
drolysis compared to DA pretreatment, which results in the
nearly complete digestion of CELF-pretreated corn stover
solids.
From a different perspective, the change of reaction rate co-
efficient kt with respect to hydrolysis time for both DA and
CELF pretreatments is shown in Figure 5B. The temporal pro-
gression of kt from the CELF-pretreated corn stover at 2 and
5 mgenzyme gglucan
À1
loadings was consistently 3–4 times greater
than that of DA-pretreated corn stover at corresponding
enzyme loadings, which validates the superior enzymatic reac-
tivity of CELF-pretreated corn stover. As DA and CELF removed
similar levels of hemicellulose, these results can be attributed
to the extensive removal of lignin during CELF pretreatment,
which results in less cellulose surface blockage and enzyme in-
hibition than that of DA pretreatment. Wang et al.[20]
proposed
that a smaller h value correlates with less lignin inhibition, and
a lower h value was observed for CELF-pretreated corn stover
(0.169 at 5 mgenzyme gglucan
À1
) in comparison to DA-pretreated
material at the same enzyme loadings (0.607 at
5 mgenzyme gglucan
À1
; Table S1). Future work with CELF pretreat-
ment will be coupled with fractal kinetic modeling to further
investigate how delignification by CELF pretreatment affects
substrate–enzyme interactions.
Changes resulting from lignin removal by CELF observed by
SEM
An SEM comparison is shown in Figure 6 of the macro- and mi-
crostructure between raw corn stover and solids produced by
DA and CELF pretreatments to aid us to understand mecha-
nisms that could account for the extraordinary reactivity of
CELF-pretreated corn stover with cellulolytic enzymes. As
a result of the heterogeneous distribution of raw corn stover,
particles with common surface features were imaged for com-
parison. The outer structure of raw corn stover appears porous
with sheetlike pleats that surround the open vascular networks
used for water and nutrient delivery to the plant (Figure 6A). If
the corn stover was pretreated with DA, the macrostructure of
the solids was changed by the destruction of the sheetlike
walls to reveal the porous vascular network underneath (Fig-
ure 6B), which is likely a primary feature to improve accessibili-
ty for enzyme attack. The significant amount of lignin still pres-
ent in solids following DA pretreatment apparently preserves
the major features of raw corn stover. In contrast, CELF altered
the macro- and microstructural features that are vital for the
efficient deconstruction of lignocellulosic biomass significantly
(Figure 6C),[7a]
which is likely caused by extensive lignin remov-
al that collapses most of the superstructure so that neither the
sheetlike walls nor the vascular channels can be distinguished
easily. This drastic destruction and collapse shown in the dried
cell-wall structure after CELF pretreatment may be responsible
for the sustained reactivity of the substrate to enzymatic hy-
Figure 5. Comparison of the change in fractal kinetic rate coefficient with re-
spect to: A) percent conversion in the higher glucan conversion regime of
60–100% in which the accessible substrate surface area had decreased sig-
nificantly for CELF pretreatments at 5 mgenzyme gglucan
À1
(CELF, 5 mg) and DA
pretreatments at 15 and 30 mgenzyme gglucan
À1
(DA, 15 and DA, 30 mg respec-
tively) and B) enzymatic hydrolysis time for the DA and CELF pretreatments
at low loadings of 2 and 5 mgenzyme gglucan
À1
(denoted as DA/CELF, 2 mg and
DA/CELF, 5 mg, respectively).
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6. drolysis. The visible “wrinkling” of the material after CELF pre-
treatment was likely because of the drying of the sample,
which indicates that the material may be structurally weaker
and become expanded readily if rehydrated by water, some-
what like a sponge. Our next steps include the application of
13
CP NMR spectroscopy and Simons’ staining and water reten-
tion to compare the relative effects of CELF and DA pretreat-
ments on crystallinity and accessibility, respectively, as well as
to record more extensive SEM images and particle size distri-
butions to test these hypotheses.
Simultaneous saccharification and fermentation of pretreat-
ed corn stover to ethanol
We applied SSF to both CELF- and DA-pretreated solids to
demonstrate the compatibility of CELF pretreatment with the
achievement of high ethanol yields by fermentation. SSF com-
bines the enzymatic hydrolysis of biomass to sugars with sugar
fermentation to ethanol in a single step to reduce the end-
product inhibition of enzymes by high soluble sugar concen-
trations and thereby increase ethanol yields and titers.[10,21]
In
this study, SSF was applied to pretreated solids in 125 mL
shake flasks at 4 wt% glucan loading; each flask contained
50 mL working volume and was fitted with a bubble trap and
inoculated with the D5A strain of S. cerevisiae yeast along with
Accellerase 1500. The ethanol yields obtained if SSF was ap-
plied to solids produced by DA and CELF pretreatments under
optimized conditions compared to yields from an Avicel cellu-
lose control at loadings of 5 and 15 mgenzyme gglucan
À1
are shown
in Figure 7A and B. These results show that although a concern
of solvent-based pretreatment,
such as with ionic liquids, can be
the toxicity of residual solvent in
pretreated solids towards en-
zymes or microbes that would
reduce ethanol yields, simply
washing CELF-pretreated solids
with water through a vacuum
filter was sufficient to achieve
high yields by SSF. Furthermore,
consistent with our results for
just enzymatic hydrolysis of the
same solids, higher SSF ethanol yields were obtained for solids
from CELF pretreatment at both enzyme loadings. For the
higher loading of 15 mgenzyme gglucan
À1
, the ethanol yield pla-
teaued at approximately 90 and 83% of the theoretical yield
for solids from CELF and DA pretreatments, respectively, and
the yield increased much more rapidly for the CELF-pretreated
solids (Figure 7A). However, Avicel microcrystalline cellulose
was more recalcitrant than corn stover solids produced by
either pretreatment, and the ethanol yields were still increasing
at ~300 h fermentation time. These results suggest that, unlike
CELF-pretreated material, the high lignin content of DA-pre-
treated corn stover and the lower enzyme accessibility of crys-
talline Avicel limit the effectiveness of hydrolytic enzymes and
reduce overall ethanol yields. The differences are even more
dramatic at a more commercially affordable enzyme loading of
5 mgenzyme gglucan
À1
, for which yields from CELF-pretreated solids
peaked at over 90% in only four days, whereas the yield for
DA-pretreated solids was only approximately 50% after six
days. Thus, CELF pretreatment gave a superior conversion of
corn stover to ethanol compared to either of the other two
substrates to achieve ~90% or higher ethanol yields consis-
tently at both 15 and 5 mggglucan
À1
enzyme loadings. Future
studies will optimize SSF ethanol yields from CELF-pretreated
solids at higher solid concentrations to realize more economi-
cally attractive ethanol titers.
The yields of metabolites after seven days of culture to close
material balances on sugars are shown in Figure 7C. More
glycerol was produced by the conversion of CELF- than DA-
pretreated corn stover solids, likely because of the greater os-
motic stress generated by the higher initial glucose concentra-
Figure 6. SEM images of solids at 1000X magnification from A) raw corn stover, B) DA-pretreated corn stover
(1608C, 0.5 wt% sulfuric acid, 20 min), and C) CELF-pretreated corn stover (1508C, 0.5 wt% sulfuric acid, 25 min).
Scale bar is shown.
Figure 7. Ethanol yields from SSF of solids from DA and CELF pretreatment of corn stover and Avicel PH-101 cellulose versus culture time at A) 15 mggglucan
À1
and B) 5 mggglucan
À1
loading of Accellerase 1500 enzyme. C) Cumulative yields [%] of SSF metabolites from a seven day culture.
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7. tions[22]
or higher ethanol concentrations at the completion of
the fermentation. Additional optimization to reduce residual
glucose concentrations during culture may further improve
ethanol yields. Acetic acid and cellobiose concentrations re-
mained minimal throughout the fermentation for each of the
samples. Thus, ethanol yields from SSF were mostly governed
by the extent of sugar release by enzymes and not by yeast
performance.
The integration of CELF pretreatment with SSF to produce
ethanol from lignocellulosic biomass is outlined in Figure 8 in
a simplified block flow diagram. THF and sulfuric acid can be
introduced directly to wet biomass and fed to a high-solids re-
actor (i.e., a Pandia reactor) that is heated to reaction tempera-
ture by direct steam injection. After the CELF reaction, depres-
surization of the contents at the reactor exit decreases the
temperature rapidly to 1008C to quench further reaction. The
solids from the reactor can then be separated from the liquids
and washed with water in a countercurrent belt filter to
remove soluble inhibitors released in pretreatment and limit
sugar dilution. The liquids are then delivered to a distillation
island in which THF can be recovered. Although THF forms
a 95% azeotrope with water, further energy-intensive separa-
tion is not required because the recycled THF stream does not
require a high purity.[13]
Furthermore, the CELF process is inher-
ently aqueous based and does not require distillation of THF
to dryness, which avoids the concentration of THF peroxides
to dangerous levels. If needed, peroxide destruction methods
practiced industrially, such as caustic soda treatment, can be
implemented without detriment to the process. Upon the re-
moval and recovery of THF, the dissolved lignin product pre-
cipitates as a solid that could potentially be upgraded catalyti-
cally to valuable chemicals and fuel products or burned to pro-
vide process heat and power. Neutralization and conditioning
of the liquid stream by a suitable base (e.g., overliming with
calcium hydroxide) is applied to make the dissolved xylose and
arabinose released during pretreatment suitable for biological
fermentation. Although Figure 8 shows that both the liquid
and washed-solid streams feed the same SSF operation, the
liquid stream rich in xylose and arabinose from CELF pretreat-
ment could be fed to one fermentation train and the cellulose-
rich solids fed to a separate SSF operation. In the latter case,
micro-organisms engineered for the fermentation of dissolved
xylose and arabinose sugars could be employed in the first fer-
menter, and conventional yeast such as S. cerevisiae could be
employed for the combined enzymatic hydrolysis and fermen-
tation of the cellulose-rich solids in the second, with high etha-
nol yields expected based on the results in this study. Our
future work will comprise fermentation of the soluble sugars
from Stage 1 to ethanol.
Conclusions
THF is a biomass-sourced green solvent with catalytic qualities
that promotes biomass deconstruction and delignification. We
have shown a significant augmentation of traditional DA pre-
treatment by application of THF as a miscible co-solvent,
which represents a significant advancement in pretreatment
technology. Optimization of this pretreatment strategy, co-sol-
vent-enhanced lignocellulosic fractionation (CELF), at 1508C
with 0.5 wt% sulfuric acid resulted in total (arabinan, xylan,
and glucan) combined (Stage 1+Stage 2) sugar yields of ~95%
of the theoretical maximum at a low enzyme loading of
2 mggglucan
À1
. Unlike DA pretreatment, yields from the enzy-
matic hydrolysis of solids from the CELF pretreatment of corn
stover remained high over a wide range of pretreatment times,
such that optimization of the process could focus on the maxi-
mization of the xylose recovery in Stage 1. The exceptional
sugar yields from the enzymatic hydrolysis of CELF-pretreated
solids also translated into an excellent simultaneous saccharifi-
cation and fermentation (SSF) performance with S. cerevisiae
D5A of over 90% ethanol yields at an enzyme loading of only
5 mgprotein gglucan
À1
. A process strategy was outlined such that
CELF pretreatment could be integrated with SSF to produce
ethanol directly from lignocellulosic biomass and THF could be
recycled. Future characterization of the pretreated solids on
multiple feedstocks is planned to better understand how CELF
alters the physiochemical fea-
tures of biomass and enhances
sugar yields.
CELF also provided new in-
sights into promising pretreat-
ment strategies that could en-
hance enzymatic hydrolysis. By
tracing the fate of the primary
components in biomass after DA
and CELF pretreatments, we
showed that virtually complete
lignin removal was the key dif-
ference that could account for
the enhanced enzymatic hydrol-
ysis of the solids from CELF pre-
treatment. Our fractal kinetic
analysis of the experimental en-
zymatic hydrolysis data also
pointed to lignin removal by
Figure 8. Simplified block flow diagram of a proposed biomass conversion process that integrates CELF pretreat-
ment with SSF to produce ethanol.
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8. CELF that resulted in higher accessibility and less inhibition to-
wards cellulolytic enzymes than that possible for DA pretreat-
ment. SEM images showed that extensive lignin removal by
CELF pretreatment apparently altered the vascular and support
structures of corn stover dramatically such that the cell walls
were completely collapsed and the material appeared “wrin-
kled” after air-drying.
Experimental Section
Compositional analysis of corn stover was performed according to
the established NREL procedure (version 8-03-2012) in triplicate.
The resulting mass composition was (37.1Æ0.7)% glucan, (25.1Æ
0.3)% xylan, (4.2Æ0.1)% arabinan, (14.5Æ0.4)% K-lignin, and
28.0% other materials.[23]
Other materials are usually composed of
ash (4–6 wt%), proteins (2–3 wt%), acetic acid (2–4 wt%), sugar
acids (1–2 wt%), and extractives (2–8 wt%) that were not quanti-
fied in this study.[24]
Frozen stock of Saccharomyces cerevisiae (D5A)
was prepared from plate monocultures that were transferred and
cultured in a shaker incubator at 150 rpm and 388C in yeast pep-
tone dextrose (YPD) media that contained yeast extract (10 gLÀ1
),
peptone (20 gLÀ1
), and glucose (50 gLÀ1
). After 24 h incubation,
a 40 wt% glycerol in water solution was added, and 1 mL aliquots
of the resulting mixture were transferred to sterile cryovials and
placed in a À708C freezer. Before each SSF run, the inoculum was
prepared by thawing, transferring, and growing the frozen stock
on a shaker incubator at 150 rpm and 378C for 12 h in 250 mL baf-
fled flasks with YPD medium. The inoculum was then centrifuged
and resuspended in sterile deionized (DI) water twice for washing
and prepared for inoculation at a 0.5 optical density (O.D.).
Analytical procedures
All chemical analyses were based on Laboratory Analytical Proce-
dures (LAPs) documented by NREL (Golden, CO; http://www.nrel.-
gov/biomass/analytical_procedures.html). Liquid samples along
with appropriate calibration standards were analyzed by HPLC
(Waters Alliance 2695 system equipped with a Bio-Rad Aminex
HPX-87H column and Waters 2414 refractive index (RI) detector)
with an eluent (5 mm sulfuric acid) flow rate of 0.6 mLminÀ1
. The
chromatograms were integrated by using Empower 2 software
package (Waters Co., Milford, MA). As developed and practiced
consistently in our laboratory,[16,25]
combined total sugar yields
(Stage 1+Stage 2) from each pretreatment were determined as the
sum of the total mass of soluble glucose, xylose, and arabinose re-
leased by pretreatment (Stage 1) plus the total mass of these three
sugars released by saccharification of the washed pretreated solids
with enzymes (Stage 2, enzymatic hydrolysis). Details of the calcu-
lation of sugar yields are outlined in the Supporting Information.
As a result of their greater abundance in corn stover composition,
total sugars were considered to include glucose, xylose, and arabi-
nose. The total lignin recovered was calculated from the mass of
total unwashed K-lignin precipitated upon recovery of THF, where-
as delignification was calculated from the percentage of K-lignin
that remained in the pretreated material compared to the initial K-
lignin content of the raw material.
Pretreatment of corn stover
Pretreatment reactions were performed in a 1 L Hastelloy Parr au-
toclave reactor (236HC Series, Parr Instruments Co., Moline, IL)
equipped with a double stacked pitch blade impeller rotated at
200 rpm. The THF co-solvent mixture for CELF pretreatment con-
tained a 1:1 volume ratio of THF (99% purity, Fisher Scientific,
Pittsburgh, PA) and water. A 0.5 wt% sulfuric acid (Ricca Chemical
Company, Arlington, TX) concentration was found to achieve the
highest total glucose+xylose+arabinose yield from DA alone or
CELF pretreatment coupled with subsequent enzymatic hydroly-
sis.[16]
Before each reaction, corn stover was added to the acid solu-
tion and soaked overnight at 48C. Corn stover solid loadings were
5 wt% for both the CELF and DA pretreatments based on the total
working mass of liquids and solids in the reaction. All reactions
were maintained at temperature (Æ28C) by convective heating by
using a 4 kW fluidized sand bath (Model SBL-2D, Techne, Princeton,
NJ), and the reactor temperature was measured directly by using
an in-line thermocouple (Omega, K-type). The sand bath tempera-
ture was set to 3408C to reduce the heat-up time to under
3 min.[26]
At the conclusion of each reaction, the reactor was
cooled by submerging quickly it in a large water bath at RT. The
solids were then separated from the reaction liquor by vacuum fil-
tration at RT through glass fiber filter paper (Fisher Scientific, Pitts-
burgh, PA). The mass and density of the liquid fractions were mea-
sured to complete accurate yield calculations. As a result of differ-
ences in density between the co-solvent mixtures and pure water,
final densities were determined by weighing 25 mL of the reacted
liquid in a volumetric flask after each reaction. Liquid samples were
analyzed by HPLC as described previously.
Enzymatic hydrolysis of pretreated corn stover and Avicel
cellulose
As noted in the NREL standard protocol,[27]
enzymatic hydrolysis of
pretreated materials was performed in triplicate using 125 mL Er-
lenmeyer flasks with a 50 g total working mass that contained
50 mm citrate buffer (pH 4.8) to maintain pH, 0.02% sodium azide
to prevent microbial growth, and approximately 1 wt% glucan
from pretreated solids or Avicel PH-101 cellulose (Sigma Aldrich, St.
Louis, MO). The cellulase enzyme (Accellerase1500, DuPont Indus-
trial Biosciences, Palo Alto, CA) loadings were varied from 2–
30 mgenzyme gglucan
À1
based on the mass of glucan in the raw corn
stover, as described elsewhere,[28]
and not according to the glucan
content of the pretreated material to provide a useful comparison
among different pretreatments.[5a,6b,29]
Enzyme loadings based on
the raw material are important because a pretreatment should not
be penalized for releasing sugars before enzymatic hydrolysis, as
total sugar yields from both Stage 1 (pretreatment)+Stage 2 (enzy-
matic hydrolysis) should be maximized.[30]
The flasks that contained
biomass slurry were placed in a Multitron orbital shaker (Infors HT,
Laurel, MD) set at 150 rpm and 508C and allowed to equilibrate for
1 h before the addition of enzyme. Samples of approximately
0.75 mL were taken periodically into 2 mL centrifuge vials (Fisher
Scientific, Pittsburgh, PA) from each flask and centrifuged at
14000 rpm for 5 min to determine the progress of the enzymatic
hydrolysis. The supernatant was then transferred into 500 mL HPLC
vials (Grace Davison, Deerfield, IL) for HPLC analysis.
Fractal modeling of hydrolysis kinetics
A fractal model based on first-order chain breakdown to form glu-
cose was found to best describe cellulose hydrolysis with the rate
coefficient kt related to the hydrolysis time raised to the fractal ex-
ponent h [Eq. (1)]:[31]
dC
dt
¼ ktC, in which kt ¼ ktÀh ð1Þ
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Full Papers
9. The model described by Equation (2) was used to fit the experi-
mental data from the enzymatic hydrolysis by nonlinear regression
using MATLAB 7.0 (damped least squares) in which X [%] is the
conversion and t [h] is time:
X ¼ 100 Ã 1 À exp Àk 1 þ
t1Àh
À 1
1 À h
! '
ð2Þ
Cell cultivation and SSF
Consistent with NREL standard protocols,[32]
SSF was performed in
triplicate in 125 mL flasks with a 50 g working mass that contained
citrate buffer (50 mm, pH 4.8), yeast extract (10 gLÀ1
, Becton, Dick-
inson and Company, Redlands, CA), peptone (20 gLÀ1
, Becton,
Dickinson and Company, Redlands CA), tetracycline (40 mgLÀ1
,
Sigma Aldrich, St. Louis, MO) as an antimicrobial agent, Accellerase
1500 cellulase (loaded at 5 or 15 mgprotein gglucan
À1
), and D5A frozen
stock culture. DI water and solids were loaded into flasks (with at-
tached bubble traps) to achieve a 4 wt% glucan loading of either
the pretreated solid residues or Avicel PH 101 cellulose, and
masses of the whole flask assembly were recorded before autoclav-
ing at 1218C for 30 min. Flasks were then cooled, reweighed, and
moved into a laminar flow hood (Baker and Baker Ruskinn, Sanford,
ME) for aseptic readdition of presterilized DI water to replenish
water loss, yeast extract, citrate buffer, tetracycline, Accellerase
1500 cellulase, and cell inoculum.
SEM imaging
A field-emission scanning electron microscope (Philips XL-30) was
used to provide images of the raw, pretreated, and post-enzymatic
hydrolysis corn stover. Air-dried samples of each were placed on
pin-stub mounts with carbon tape and sputter coated with Pt by
using a Cressington 108 Auto system (Ted Pella Inc, Redding CA).
The surface macro- and microstructures of the samples were char-
acterized at an acceleration voltage of 2 kV.
Acknowledgements
We are grateful for funding by the Office of Biological and Envi-
ronmental Research in the Department of Energy (DOE) Office of
Science through the BioEnergy Science Center (BESC) at Oak
Ridge National Laboratory (Contract DE-PS02-06ER64304), the
National Science Foundation (Grant #2013142496), and the Uni-
versity of California Transportation Center (UCTC) for making this
research possible. We also acknowledge the Center for Environ-
mental Research and Technology (CE-CERT) of the Bourns College
of Engineering for providing the facilities and the Ford Motor
Company for funding the Chair in Environmental Engineering
that facilitates projects such as this one. We would like to ac-
knowledge Dr. Taiying Zhang for her contribution to the incep-
tion of this paper.
Keywords: biomass · enzymes · hydrolysis · renewable
resources · solvent effects
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Full Papers
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Received: September 24, 2014
Revised: December 7, 2014
Published online on , 0000
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Full Papers
11. FULL PAPERS
T. Y. Nguyen, C. M. Cai, R. Kumar,
C. E. Wyman*
–
Co-solvent Pretreatment Reduces
Costly Enzyme Requirements for High
Sugar and Ethanol Yields from
Lignocellulosic Biomass
Break it down! We describe a new pre-
treatment approach, co-solvent-en-
hanced lignocellulosic fractionation
(CELF), that reduces plant recalcitrance
by solvating biomass lignin using acidi-
fied aqueous THF solutions to improve
sugar yields and reduce enzyme re-
quirements for saccharification. Our re-
sults provide important insights into
promising biomass pretreatment
strategies.
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These are not the final page numbers! ÞÞThese are not the final page numbers! ÞÞ