The invention relates in general to methods of processing lignocellulosic biomass and to methods of pre-treatment of lignocellulosic biomass. In particular, the invention provides methods which fix moisture levels in lignocellulosic biomass to levels near the inherent water holding capacity of the material.
Bioethanol offers a promising alternative to fossil fuels, providing renewable and “carbon neutral” energy sources that do not disrupt global atmospheric carbon dioxide balance. Amongst other possible sources of bioethanol precursors, lignocellulosic biomass can be enzymatically hydrolysed to provide fermentable carbohydrates. However, because of its complex chemical structure, lignocellulose can only be efficiently hydrolysed by presently known enzyme activities after some pre-treatment that renders cellulose fibers accessible to enzyme catalysis. Such pre-treatment processes typically involve heating to comparatively high temperatures, between 100 and 250° C. Large scale bioethanol production from lignocellulosic biomass requires large scale pre-treatment and processing. Accordingly, an intense interest has arisen in methods of biomass pre-treatment and processing that reduce costs or otherwise increase commercial viability of bioethanol on production scale.
Two factors which heavily influence overall costs of bioethanol production from lignocellulosic biomass are energy costs of ethanol distillation from fermentation mixtures and energy costs of biomass pre-treatment.
Energy costs of ethanol distillation can be greatly reduced where ethanol content of fermentation mixtures exceeds 4%. However, to achieve these high ethanol levels in fermentation mixtures, without requiring costly and inefficient additional process steps, enzymatic hydrolysis of pre-treated lignocellulosic biomass should be conducted at relatively high dry matter content (DM)—at least about 15-20%. Previous attempts to achieve high DM content in fermentation mixtures have been hampered by accumulation of fermentation inhibitors generated during pre-treatment and by other problems arising during enzyme hydrolysis and fermentation. See e.g. refs. 1-7.
Recently, however, production scale methods for enzyme hydrolysis of pre-treated lignocellulosic biomass have been reported that are efficient and effective at DM greater than 20%. These methods provide liquefaction and saccharification of biomass using “free fall” mixing, as described by WO 2006/56838 (ref. 8), which is hereby incorporated by reference in entirety.
Energy costs of pre-treatment can be reduced where biomass is pre-treated at high DM. Greater dry matter content of biomass corresponds with reduced aqueous content. Thus, the greater the dry matter content of biomass during pre-treatment, the less energy is wasted heating aqueous content. It is, thus, generally advantageous during pre-treatment to achieve the highest possible DM levels (lowest possible aqueous levels) of lignocellulosic biomass that do not contribute to eventual reduction of ethanol yield (% theoretical) from fermentation mixtures.
Optimal pre-treatment conditions require that biomass have some aqueous content. Eventual ethanol yield (% theoretical) from lignocellulosic biomass is generally improved to the extent that it is pre-treated under conditions in which cellulose fibers do not contain air. Biomass that is simply exposed to moisture can, eventually, with time, achieve homogenous aqueous saturation of cellulose fibers. However, such an “impregnation” approach is slow, and accordingly unsuitable for production scale pre-treatment. Aqueous content of biomass has been previously optimized on production scale by soaking and pressing prior to pre-treatment, for example, as described by WO 2007/009463 (ref. 9), which is hereby incorporated by reference in entirety. After soaking in an excess of aqueous solution, then pressing to remove as much aqueous content as possible, lignocellulosic biomass will typically comprise a “saturation level” of aqueous content corresponding to DM greater than about 30%.
While such soaking and pressing methods are effective, they require additional energy for pressing, time delays for soaking, as well as additional process steps. These introduce additional costs and production inefficiencies.
Accordingly, it is advantageous to provide methods of processing lignocellulosic biomass, suitable for use in continuous processing on production scale, that provide homogenous, aqueous saturation of cellulose fibers quickly, with low energy cost, and with the fewest possible process steps.
In some embodiments, the invention provides methods of processing lignocellulosic biomass whereby biomass is wetted with an amount of aqueous solution sufficient to provide moisture levels near the inherent water holding capacity of the material then thoroughly mixed, optionally using a mixer that massages water content into lignocellulosic fibers.
As used herein, the following terms have the following meanings:
Lignocellulosic biomass refers to material derived from plants or other organisms in which carbohydrate content is substantially cellulose and hemicellulose and which comprises more than 5% lignin. Cellulose is a polysaccharide composed of
Dry matter refers to insoluble material. Typically, dry matter comprises insoluble fibers.
(iii). Inherent Water Holding Capacity of the Biomass.
Inherent water holding capacity of the biomass refers to the amount of water, or aqueous solution, that remains after repeated “pressing” in a biomass that has been “soaked” in a “soaking and pressing” process such as that described in WO 2007/009463.
Fixed dry matter content refers to moisture content of lignocellulosic biomass adjusted prior to pre-treatment and/or enzymatic hydrolysis. The dry matter content is adjusted or “fixed” by adding a quantity of water, or aqueous solution comprising one or more chemical additives, sufficient to provide moisture levels between 80-120% of the inherent water holding capacity of the biomass then thoroughly mixing. Mixing is “thorough” where substantially all of the dry matter of the lignocellulosic biomass is wetted by added water or aqueous solution. Dry matter content is “fixed” where substantially all of the water, or aqueous solution, is incorporated within fibers with substantially no excess water, or aqueous solution, that is not incorporated within fibers, except an amount not exceeding an amount of water, or aqueous solution, added in excess of 100% of the inherent water holding capacity of the biomass. Soaking typically involves excess water, >120% of the inherent water holding capacity of the biomass, that is not incorporated within fibers and does not provide fixed dry matter content as used herein.
Water content is massaged into wetted biomass fibers by subjecting them to a form of mixing that acts to alternately compress fibers then restore them to a relaxed state. An example of a mixer that massages water content into wetted biomass fibers is the Cormall Multimix MTX two auger livestock feed mixer.
Pre-treatment refers to a manipulation of lignocellulosic biomass that renders its cellulosic component more accessible to enzymes that convert carbohydrate polymers into fermentable sugars. Heat pre-treatment refers to a pre-treatment in which biomass is heated to temperatures of 100° C. or more.
(vii). Enzymatic Hydrolysis
Enzymatic hydrolysis refers to treatment of a lignocellulosic biomass with a mixture of enzyme activities comprising one or more cellulytic enzyme in such manner as to convert cellulose content to carbohydrates with at least 20% theoretical yield.
Some embodiments provide a method of processing lignocellulosic biomass comprising;
Other embodiments provide a method of processing lignocellulosic biomass comprising;
Embodiments of the invention may be practiced in batch, semi-continuous or continuous modes of operation.
In preferred embodiments, the dry matter content is fixed to levels corresponding to moisture content of greater than 85% but less than 100% of the inherent water holding capacity of the biomass. In more preferred embodiments, the dry matter content is fixed to levels corresponding to moisture content of greater than 95% but less than 100% of the inherent water holding capacity of the biomass. In still more preferred embodiments, other embodiments, the dry matter content is fixed to levels corresponding to moisture content about 100% of the inherent water holding capacity of the biomass.
In preferred embodiments, dry matter content of lignocellulosic biomass is fixed on a large scale, having dry matter mass at least 40 kg, or having dry matter mass greater than 50 kg, or greater than 100 kg, or greater than 1000 kg, or greater than 10,000 kg.
In the practice of some embodiments, any suitable lignocellulosic biomass feedstock having intrinsic dry matter content greater than about 50% may be used including at least corn stover, wheat straw, rice straw, bagasse, corn fiber, hardwood bulk, softwood bulk, nut shells, corn cobs, grasses, including but not limited to coastal Bermuda grass and switch grass, paper, including newspaper, waste papers and paper from chemical pulps, sorted refuse, cotton seed hairs, empty fruit baskets and other materials well known in the art.
The lignocellulosic biomass may be pre-processed by chopping, grinding, ball milling, or other mechanical treatment processes.
In preferred embodiments, a lignocellulosic biomass will have a distribution of particle sizes prior to pre-treatment having 80% falling within the range of 1 to 10 cm. In other embodiments, a lignocellulosic biomass will have a distribution of particle sizes having 80% falling within the range of 0.5 to 15 cm.
In practice of preferred embodiments, it is helpful to determine the inherent water holding capacity of a lignocellulosic biomass, for example, by measuring the moisture content that remains after “pressing” in a biomass that has been “soaked” in a “soaking and pressing” process such as that described in WO 2007/009463. For example, wheat straw typically has an inherent water holding capacity corresponding to about 42% DM.
In preferred embodiments, intrinsic DM content of a lignocellulosic biomass is first determined by means of drying to no loss of weight or by any method known in the art. A quantity of water, or aqueous solution, sufficient to provide moisture levels between 80-120% of the inherent water holding capacity of the biomass can then be readily determined based on the dry mass of the lignocellulosic biomass. For example, for 10,000 kg of wheat straw having dry matter content 92.0%, 30,000 liters of water or aqueous solution should be added to provide dry matter content of about 30% (moisture content about 120% of the inherent water holding capacity). For the same lignocellulosic biomass, to provide dry matter content of about 40% (moisture content about 103% of the inherent water holding capacity), only 23,000 liters of water or aqueous solution need be added.
In other embodiments, dry matter content of a lignocellulosic biomass can be estimated visually, or based upon reference materials or prior experience.
In other embodiments, an appropriate amount of water or aqueous solution can be approximated or added in amounts that may vary within constraints of some process limitations such as water availability. For example, dry matter content may be fixed imprecisely at between 30-40% by adding an amount of water or aqueous solution that is not precisely measured, although sufficient, in that it does not exceed the amount required for 30% dry matter.
Aqueous solutions suitable for practice of some embodiments may comprise acids, bases, salts, metals, or other chemical additives, enzymes or microorganisms. In preferred embodiments, a mildly acidic solution is added. Optimum pH is typically between 3.5-4.0. This lowers heat requirements for pre-treatment and prevents sticking of “cooked” biomass to reactor vessels or communication lines. Wash effluent or extracts of pre-treated biomass, typically containing acetic acid, may be added as aqueous solutions suitable for practice of some embodiments.
In preferred embodiments, the lignocellulosic biomass and added water or aqueous solution may be mixed thoroughly using a mixer that massages water content into lignocellulosic fibers. One such mixer, suitable for practice of preferred embodiments, is illustrated in
In other embodiments, the lignocellulosic biomass and added water or aqueous solution may be mixed thoroughly using a mixer that imparts a combination of shear and/or pressing forces such that the biomass is mixed thoroughly within 60 minutes, or, optionally, within 30 minutes, or, optionally, within 20 minutes, or, optionally, within 10 minutes. In still other embodiments, the lignocellulosic biomass and added water or aqueous solution may be mixed by any means that provides that, within 60 minutes, or, optionally, within 30 minutes, or, optionally, within 20 minutes, or, optionally, within 10 minutes, substantially all of the water, or aqueous solution, is incorporated within fibers with substantially no excess water, or aqueous solution, that is not incorporated within fibers.
In practice of some embodiments, water or aqueous solution may be added as cold liquid, which is typically absorbed in a shorter time, or as steam or a combination of steam and liquid. In practice of some embodiments, water or aqueous solution may be added directly in the mixer. Alternatively, water or aqueous solution may be added within a vertical column through which biomass is falling, by force or gravity or conveyance, into the mixer. Other possible arrangements can be readily imagined.
After processing by embodiments of the invention, the biomass can be pre-treated by any heat pre-treatment and, further, to any post pre-treatment processing.
In some embodiments, a biomass that does not require pre-treatment may be used. For example, waste paper and other paper pulp feedstocks, do not require heat pre-treatment but can be used directly in enzymatic hydrolysis.
These data origin from the IBUS pilot plant of Inbicon in Fredericia, Denmark. Cut wheat straw and liquid were mixed in a KUHN Euromix II type 1460 feed mixer. The dry matter content of the wetted straw after mixing was varied from 20 to 50% DM, which corresponds with moisture levels of between 138 to 86% of the inherent water holding capacity of the biomass.
500 kg of cut (2-10 cm in length) wheat straw was added to the mixer. Liquid in an adjusted amount was sprayed on the straw. Then the mixer was started, and the liquid was massaged in to the straw. Residence time in the mixer was 30 minutes. After mixing the dry matter content was measured in the wetted straw and it was found to be in agreement with the calculated. In this way samples of wetted wheat straw with a content of 20, 30, 40 and 50±1% DM were prepared. Two samples were prepared at 40% DM, which corresponds with moisture levels of about 103% of the inherent water holding capacity of the biomass.
These samples were loaded in to the pilot pre-treatment facilities of Inbicon. In this pilot plant the wetted wheat straw in a continuously way was steam treated at 185° C. for 10 minutes.
As a reference, for comparison with the “fixed dry matter” samples, soaked and pressed wheat straw was also pre-treated. In the reference sample,s cut straw was soaked for 5-10 minutes in 80° C. hot liquid. After the soaking the straw was pre-treated at a dry matter content of 18-22%, which corresponds with moisture levels of between 141 to 134% of the inherent water holding capacity of the biomass.
The pre-treatment must ensure that the structure of the lignocellulosic content is rendered accessible for enzymatic hydrolysis, and at the same time the concentrations of harmful inhibitory by-products such as acetic acid, furfural and hydroxymethyl furfural remain substantially low. Therefore, after heat pre-treatment, the pre-treated straw is washed by water or condensate then pressed. After post-pre-treatment washing and pressing, the cellulosic fibres have a dry matter content of app. 25-35%. The pre-treated straw was collected in plastic bags and stored at 1-5° C. until use.
The pre-treated wheat straw samples were evaluated regarding convertibility of cellulose in a shake flask set up at 12% DM, where the samples were simultaneous saccharified and fermented (SSF). The pre-treated fibre fraction was diluted with an acetic acid buffer, pre-hydrolysed 6 hours with Novozym 188 and Celluclast 1.5 FG at 50° C. using an enzyme loading of 5.0 FPU (g DM)−1 then simultaneously saccharified and fermented (SSF) 144 hours at 30-33° C. with common bakers yeast (Baker's yeast, De Danske Spritfabrikker).
Accordingly, by practice of embodiments of the invention, it is possible to reduce energy consumption, stream line process steps, and reduce process time without loss of yield, by reducing the water content of the biomass during pre-treatment. However, as shown in
These data origin from the IBUS pilot plant of Inbicon in Fredericia, Denmark. Cut wheat straw and liquid were mixed in a KUHN Euromix II type 1460 feed mixer. The dry matter content of the wetted straw after mixing was 35%, which corresponds to about 112% of the water holding capacity of the biomass.
500 kg of cut (2-10 cm in length) wheat straw was added to the mixer. A pre-determined amount of aqueous solution, sufficient to provide dry matter content of about 35%, was sprayed on the straw. Then the mixer was started, and the liquid was massaged in to the straw. Residence time in the mixer was varied from 10 to 30 minutes. After mixing the dry matter content was measured in the wetted straw and it was found to be in agreement with the calculated. In this way samples of wetted wheat straw with a content of 35±1% DM were prepared.
These samples were loaded in to the pilot pre-treatment facilities of Inbicon. In this pilot plant the wetted wheat straw in a continuously way was steam treated at 185° C. for 10 minutes.
The pre-treatment must ensure that the structure of the lignocellulosic content is rendered accessible for enzymatic hydrolysis, and at the same time the concentrations of harmful inhibitory by-products such as acetic acid, furfural and hydroxymethyl furfural remain substantially low. Therefore, after heat pre-treatment, the pre-treated straw is washed by water or condensate then pressed. After post-pre-treatment washing and pressing, the cellulosic fibres have a dry matter content of app. 25-35%. The pre-treated straw was collected in plastic bags and stored at 1-5° C. until use.
The pre-treated wheat straw samples were evaluated regarding convertibility of cellulose in a shake flask set up at 12% DM, where the samples were simultaneous saccharified and fermented (SSF). The pre-treated fibre fraction was diluted with an acetic acid buffer, pre-hydrolysed 6 hours with Novozym 188 and Celluclast 1.5 FG at 50° C. using an enzyme loading of 5 FPU (g DM)−1 then simultaneously saccharified and fermented (SSF) 400 hours at 30-33° C. with common bakers yeast (Baker's yeast, De Danske Spritfabrikker).
Accordingly, by practice of embodiments of the invention, it is possible to reduce energy consumption, stream line process steps, and reduce process time without loss of yield, by reducing the water content of the biomass during pre-treatment, through a processing that provides thorough mixing within 60 minutes, or, optionally, within 30 minutes, or, optionally, within 20 minutes, or, optionally within 10 minutes.
These data origin from the IBUS pilot plant of Inbicon in Fredericia, Denmark. Dried empty fruit bunches (EFB) of oil palm and liquid were mixed in a KUHN EUROMIX II™ type 1460 feed mixer.
500 kg of EFB (average fibre length of app. 5-10 cm) was added to the mixer. Liquid in an adjusted amount was sprayed on the EFB. Then the mixer was started, and the liquid was massaged in to the EFB. Residence time in the mixer was 60 minutes. After mixing the dry matter content was measured in the wetted EFB and it was found to be in agreement with the calculated. In this way samples of wetted EFB with a content of 25 and 35±1% DM were prepared.
These samples were loaded in to the pilot pre-treatment facilities of Inbicon. In this pilot plant the wetted EFB in a continuously way was steam treated at 200° C. for 12 minutes.
The pre-treatment must ensure that the structure of the lignocellulosic content is rendered accessible for enzymatic hydrolysis, and at the same time the concentrations of harmful inhibitory by-products such as acetic acid, furfural and hydroxymethyl furfural remain substantially low. Therefore, after heat pre-treatment, the pre-treated EFB is washed by water or condensate then pressed. After post-pre-treatment washing and pressing, the cellulosic fibres had a dry matter content of app. 25-35%. The pre-treated EFB was collected in plastic bags and stored at 1-5° C. until use.
The pre-treated EFB samples were evaluated regarding convertibility of cellulose in a shake flask set up at 12% DM, where the samples were simultaneously saccharified and fermented (SSF). The pre-treated fibre fraction was diluted with an acetic acid buffer, pre-hydrolysed 6 hours with ACCELLERASE 1500™ (Genencor) at 50° C. using an enzyme loading of 0.21 ml (g cellulose)-1 then simultaneously saccharified and fermented (SSF) 144 hours at 30-33° C. with common bakers yeast (Baker's yeast, De Danske Spritfabrikker). In these experiments a cellulose conversion of 88% was reached.
The examples and descriptions provide representative examples of particular embodiments and are not intended to limit the scope of the invention.
Number | Date | Country | Kind |
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PA 2008 00524 | Apr 2008 | DK | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IB09/05231 | 4/14/2009 | WO | 00 | 9/30/2010 |
Number | Date | Country | |
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61043743 | Apr 2008 | US |