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JOURNAL OF COMPUTER SCIENCE AND ENGINEERING, VOLUME 17, ISSUE 2, FEBRUARY 2013 6

A Comparative Study of Biobutanol Processes as Biofuel from Agricultural Substrates


Neo Lei Yee, Lim Soo King, and Low Chong Yu
Abstract A comparative study of biobutanol processes from various agricultural substrates was performed based on the results obtained from the current available research techniques. The most favorable economical and optimized process technique is aimed to obtain for production in industrial scale and future research study. The physical and chemical properties of biobutanol are closed to gasoline leading it to be a superior alternative biofuel as compared to other such as bioethanol. The low cost lignocellulosic substrates are widely available that has significant impact on the overall cost of biobutanol production. Pre-treatment and hydrolysis of lignocellulosic substrates, ABE fermentation, and product recovery are the major processes involved in the production of biobutanol. From the study, fed-batch fermentation integrated with in-situ gas stripping is the most favorable process and able to have an average productivity and yield of 1.16g/L.h and 0.47g/g respectively in the control experiment as compared to other process techniques like batch fermentation. Simultaneous hydrolysis and fermentation can further enhance the efficiency of the production system and reduce the overall cost of production with productivity and yield of 0.36g/L.h and 0.44g/g respectively by using wheat straw. In future study, optimization of the developed process technique and simultaneous hydrolysis and fermentation will be carried out with experiments and simulations by using sugarcane bagasse as fermentation substrates with industrial and agricultural collaborators. Index Terms ABE fermentation, biobutanol, biofuel, lignocellulosic substrates

1 OBJECTIVES

he objective of this study is to provide a fundamental concept of biobutanol as biofuel and its production from agriculture waste by introducing and comparing current available techniques from various research papers. The properties of n-butanol will be compared with conventional gasoline and ethanol as supporting details to the recent intensive research in biobutanol to replace bioethanol as better quality of biofuel. Comparison of various biobutanol production techniques along the process starting from fermentation substrate to its end product will be discussed in detailed to identify the most efficient and economical approach to be opted. Further

research can be continued to optimize the process in industrial scale which is economically competitive manner.

2 INTRODUCTION

The development of an economically viable and environmentally friendly fuel alternative is drawing increasing attention worldwide corresponds to the drastic increase of fuel price, decrease of fossil oil reserves and increase of awareness on environmental issues such as greenhouse effect and acid rain. Biofuel is any liquid fuel made from plant material which can be used as an alternative replacing petroleum-derived fuel. Intensive research and finding applications on various biofuels such as bioethanol, biobutanol, biodiesel, biomethanol, Neo Lei Yee is with the Faculty of Engineering & Science, Universiti bioDME and etc would lead to rapid growth of share of Tunku Abdul Rahman, Kuala Lumpur, Malaysia. Lim Soo King is with the Faculty of Engineering & Science, Universiti biofuels in the automotive fuel in the next decade [1]. Tunku Abdul Rahman, Kuala Lumpur, Malaysia. Among all the biofuels, biobutanol is a promising liquid Low Chong Yu is with the Faculty of Green Technology & Engineering, fuel as it is more superior as compared to the other alcoUniversiti Tunku Abdul Rahman, Kampar, Perak, Malaysia.
2013 JCSE www.Journalcse.co.uk

TABLE 1 PHYSICAL AND CHEMICAL PROPERTIES OF CONVENTIONAL FOSSIL FUEL AND ALCOHOL FUELS [1, 4, 5, 6, 7]

Molecular Formula Energy Density (MJ/L) Air-fuel Ratio Heat of Vaporization (MJ/kg) Research Octane Number (RON) Motor Octane Number (MON) Density, 20oC (kg/m3) Boiling Point (oC) Auto-ignition Temperature (oC) Flash Point (oC) Oxygen Content (% weight) Kinematic Viscosity, 20oC (cSt) Blend RVP (psi) Saturation Pressure, 38oC (kPa) Water Solubility

Gasoline C4 C12 32.5 14.6 0.36 91-99 81-89 720-775 <210 ~300 -45 to -38 0.4-0.8 7-15 31.01 Immiscible
(c)

Bioethanol C2H5OH 21.2 9 0.92 129 102 794 78.3 434 8 34.8 1.52 18-22 13.8 100%

Biobutanol C4H9OH 29.2 11.2 0.43 96 78 801 108 385 35 21.6 3.64 4.5-5.5 2.27 8.5%

hol fuels [2] due to its advantageous characteristics. Biobutanol is a four carbon alcohol derived from the fermentation of renewable resources similar to ethanol. nButanol or biobutanol is the common terms for butanol which is produced from biomass, where it is usually being assumed as a straight-chain molecule structure [1]. nButanol is produced by traditional method known as ABE (Acetone-Butanol-Ethanol) fermentation with Clostidium acetobutylicum and Clostridium beijerinckii as two common ABE fermentation agents [3].

(d)

3 PROPERTIES OF N-BUTANOL
The physical and chemical properties of gasoline, ethanol and n-butanol obtained from various studies are summarized in Table 1. Biobutanol has significant advantages compared to bioethanol as a liquid fuel. It is also a cleaner burning biofuel [2] which leads to a healthier environment due to lesser smoke density. Comparing biobutanol with bioethanol fermentation process, bioethanol fermentation is a known and mature biotechnological process leading to broader applications. However, in todays research of biobutanol has been more intensive as compared to bioethanol due to following superiorities: (a) Higher energy density. Energy density of alcohol fuels increases with increased number of carbon atom. Four carbon atoms of n-butanol have twice the number of carbon in ethanol results in 25% more energy. Energy content of n-butanol is closed to gasoline. (b) Closer air-fuel ratio to gasoline. Standard engines running on gasoline are capable to accommodate variations in fuel by adjusting the air-fuel ratio only within certain limits or else the engine will be damaged if the ratio is out of range. n-Butanol to gasoline mixing ratio can be higher for use in standard engines instead of ethanol.

(e)

(f)

(g)

(h)

Higher blending ratio. Blending of n-Butanol and gasoline can be at higher ratio for the use in existing refineries without retrofitting the engine, whereas ethanol can only be mixed at a percentage of ~10% for effective use in conventional internal combustion engines. Less ignition problems. Since the heat of vaporization of n-butanol is halved the bioethanol and slightly higher than gasoline, igniting an engine running on n-butanol in cold weather is easier [1]. Less detonation. Octane rating is a standard measurement indicating the fuels ability to resist detonation. Ability of fuel to withstand compression increases with increasing octane number. nButanol has octane rating closed to gasoline that able to reduce engine knocking. Lower volatility. Saturation pressure is a measure of volatility and it decreases with increasing carbon atom number. There will be fewer tendencies for n-butanol to undergo vapor lock problem and cavitation. Higher flash point also contributed to safer use in high temperature. Easier distribution. n-Butanol is less corrosive and better tolerance with water contamination as compared to ethanol, thus it can be distributed via existing petroleum distribution infrastructure [8]. n-Butanol also can be directly used in existing automotive engine without any modifications. Water insoluble. n-Butanol does not absorb water or sludge, phase separation occurs during blending. It is less polar and thus will remain in its hydrocarbon phase when it comes in contact with water. Alcohol fuels quality is maintained thus, there will be no dilution of gasolines octane number.

TABLE 2 COMPOSITION OF VARIOUS LIGNOCELLULOSIC MATERIALS FOR BIOFUELS

Percent Composition (%) Cellulose Hemicellulose Extractive Ash Lignin Uronic Acids Starch Wax
Reference

Barley Straw 42 28 11 7 [4]

Wheat Straw 32 23 13 10 17 2 [11]

Cassava Bagasse 25 9 10 43 [12]

Sugarcane Bagasse 43.6 33.5 2.3 18.1 0.8


[13]

Switchgrass 35 26 14 6 17 2 [11]

Hybrid Poplar 42 21 2 1 25 3 [11]

Corn Stover 36 25 6 11 18 3 [11]

4 PROCESS TECHNIQUES OF N-BUTANOL


4.1 Fermentation Substrates Over the past decades, there has been development on the production of biofuels from fermentation using agriculturally based substrates. Traditional substrates include corn, potato, sugarcane, molasses, whey permeate, etc. During the beginning stage of research, the production of biobutanol appears to be not cost effective due to conflicts between food demand and feed for fuel production [9]. The increasing demand in the market resulted in high price of food-based substrates, which become the main reason in the unfavorable economics of the process. As evaluated in past economic analysis, the cost of production heavily depends on the cost of substrate as it contributes about 63% on the total cost of production [10]. Therefore, in an effort in reducing the cost of biobutanol production, an alternative to the use of foodbased substrate is agriculture biomass, also known as lignocellulosic material. Lignocellulosic materials are mainly comprises of cellulose, hemicellulose and lignin, including wood (hardwood), by-products from corn milling (corn fibre), whey permeate, agriculture residues (wheat straws, barley straws), etc [9]. Nevertheless, these agriculture residues had proven to be valuable substrates that can be converted into n-butanol and other products in the recent studies [2]. Table 2 shows the composition of various lignocellulosic substrates used in the production of alcohol fuels. Fig. 1 shows the price comparison of lignocellulosic and non-cellulosic substrates. It has shown a significant difference as glucose and other noncellulosic substrates are having much higher cost compared to lignocellulosic substrates. The use of lignocellulosic substrates has becoming more favorable due to its wide availability, low cost of feedstocks and sugar composition [14]. In order to use linocellulosic material as substrates, both lignin and hemicellulose from cellulose have to be separated by undergoing pretreatment and hydrolysisprocess. Furthermore, these processes are able to increase porosity of material and reduce crystallinity of cellulose, thus enhancing the effectiveness of cellulose hydrolysis [15] in producing hydrolysate for fermentation.
Price ($/kg)

1.2 1 0.8 0.6


Non-cellulosic substrates Lignocellulosic substrates

0.4 0.2 0

Fig. 1. Cost of lignocellulosic and non-cellulosic substrates based on global market in 2011 including transport costs [4]

4.2 n-Butanol Producing Cultures n-Butanol is naturally formed by a number of sporeforming, rod-shaped Gram positive bacteria known as clostridia which is typically an anaerobic microorganism [1]. Different categories of Clostridia have been categorized based on their types and ratio of solvent produced. The most commonly used microbial strains in n-butanol production are Clostridium acetobutylicum and Clostridium beijerinckii. Unlike natural ethanol producing strains (yeast), the Clostridium species have an added advantage as they are able to consume both hexose and pentose sugars simultaneously that are present in biomass hydrolysates [16]. As reported in Qureshi et al. (2012), C. beijerinckii P260 is a strain that has demonstrated good productivity and yield using wheat straw hydrolysate [2]. 4.3 Pre-treatment and Hydrolysis Fig. 2 is a schematic process block diagram showing the general process of n-butanol production. Pre-treatment and hydrolysis come after the physical process of wet grinding. Many studies have shown that hydrolyzates of a variety of lignocellulosic biomass substrates are fit for

ABE fermentation. They are required to be hydrolyzed prior to fermentation by combining the pre-treatment (acid or alkali) and hydrolysis (chemically or enzymatically) techniques [17] to break the complex structure of biomass into simpler sugar. This study is focusing on the dilute sulphuric acid (H2SO4) pre-treatment and three hydrolytic enzymes hydrolysis which comprises of cellulase, -glucosidase, and xylanase as it is the commonly applied technique in biobutanol production. Dilute sulphuric acid pre-treatment is normally carried out at high temperature (121-160oC) [2]. The mixture is then cooled to ~45oC and its pH has to be adjusted to 5.0 with either sodium hydroxide (NaOH) or potassium hydroxide (KOH). The mixture shall then be hydrolysed enzymatically at 45-65oC, pH 4.2-5 and 80rpm agitation [12, 17]. Polymers of cellulose and hemicellulose are cleaved into their respective monomers by hydrolysis reaction, yielding glucose from cellulose and complete hydrolysis of hemicellulose yields hexose and pentose sugars. Unfortunately, a major problem exists with the high temperature pre-treatment is the formation of microbial inhibitors that are harmful to ABE fermentation [18]. A variety of inhibitory chemicals generated would retard the rate of fermentation or completely inhibit cell growth and biobutanol production. These inhibitors in-

clude furfurls, 5-hydroxymethylfurfural (HMF), syringaldehyde, and various acids including acetic, coumaric, glucuronic, and ferulic [2]. Treatment prior to fermentation is necessary in order to remove these inhibitors. However, it was reported that the presence of furfural and HMF within the concentration range of 0.302.00g/L will not inhibit the reaction [19]. A number of detoxification methods are developed to reduce inhibitory effects of hydrolysate, such as overliming and/or adsorbent resin/molecular sieve method to remove inhibitors, dilution method of hydrolysate and development of inhibitor tolerant/metabolizing strains [19]. Both dilution with distilled water and overliming are the more economical methods where these methods will be discussed further in the discussion section.

Fig. 2. Schematic process block diagram from lignocellulosic feedstocks to n-butanol [4]

4.4 Fermentation ABE fermentation is one of the oldest industrial known fermentation techniques which was first performed by Louis Pasteur in 1861 [12]. In terms of metabolite production, ABE fermentation shows a biphasic growth pattern which comprises of two phases. Acidogenic phase is the first stage where the major products formed are butyrate, acetate, and carbon dioxide and hydroge and it occurs during exponential growth of the bacterial culture. The second stage is known as solventogenic phase. It begins at the later stage of exponential growth phase and continues into the stationary phase of the bacterial culture. In this phase, the acids produced in previous phase will be reassimilated and converted to solvents and the main products formed are butanol, acetone and ethanol [20]. Sometime, isopropanol is produced instead of acetone by C. beijerinckii strain. The solvent ratio produced varies according to the strain and fermentation conditions. However, the typical ratio of butanol-acetone-ethanol is about 6:3:1 [21]. One of the most critical issues in ABE fermentation is solvent toxicity because the presence of ~20g/L or more solvents would cause the Clostridial cellular metabolism to cease. Low solvent concentration and productivity would then be resulted due to the limitation of carbon substrate that can be utilized by the culture [1]. During fermentation, oxygen-free N2 gas is required to purge through the medium to eliminate all oxygen and maintain anaerobic environment in the reactor after inoculation. The optimum conditions of fermentation are 35oC and pH 6.5-5.0 [17]. The conventional method of ABE fermentation is batch fermentation as studies were initiated in batch reactors. The fermentors are normally ranging in size from 100 to 200 m3 [21]. However, batch fermentation often faces challenges such as low n-butanol productivity, yield and titer, which directly leads to high cost of production [12]. Low productivity in batch reactors mainly caused byproduct inhibition, long lag phase and down time for intermediate processes such as filling, cleaning and sterilizing. Thus, the solvent yields and production solvent ratio will not be always desirable since the fermentation process has its intrinsic limitations. Advanced fermentation techniques

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were therefore being developed to overcome the limitations of batch fermentation process. When the substrate concentration in the medium is highly toxic to the culture, fed-batch fermentation is suitable to be applied instead of batch fermentation. It is initiated in batch mode at a low medium volume and low substrate concentration where it will not cause any inhibitory effect to the culture. Over time, substrates are being consumed by the fermentation microbial strains. Thus, more concentrated substrate solution is needed to be added at a slow rate to maintain the process, at the same time the detrimental substrate level must not be exceeded. The volume in the reactor will increase gradually over time. When the liquid volume has reached about 75% of the total volume of the reactor [1], the culture is then be harvested and the cycle is repeated. Fed-batch fermentation is designed in a way to utilize highly concentrated substrate, thus wastewater generated in the process and hydraulic load can be reduced. According to Ezeji, Qureshi & Blaschek (2004), reduction of product inhibition by decreasing substrate concentration is able to improve reactor productivity as there is greater cell growth in the reactor. Nevertheless, effective fed-batch fermentation must be incorporated with separation of product simultaneously since butanol is toxic to the Clostridium species [22]. Other advanced fermentation techniques are available and are aimed to improve the reactor productivity, by using continuous stirred tank reactors, immobilized cell

continuous reactors and membrane cell recycle reactors. However, discussion of these techniques are not included in this study whereas only results between batch fermentation and fed-batch fermentation are being discussed by comparing results obtained from other research papers. In addition, simultaneous saccharification and fermentation technique in both batch and fed-batch reactors are compared as well with the conventional approaches.

4.5 n-Butanol Recovery Techniques Traditional steam stripping distillation is often continued after batch fermentation in order to separate the major products formed in the reactor. High operation cost is often the major challenge exists in traditional distillation process as it is energy intensive due to n-butanol toxicity to the cultures is limited by final solvent concentration up to certain level only. Thus, high energy is required by traditional distillation to separate n-butanol in such low concentration compared to the energy content of the product itself [23]. Therefore, advanced downstream processing techniques are investigated to render a process that is economically competitive in the industry. Table 3 briefly summarizes the characteristics of various nbutanol recovery techniques such as gas stripping, perstraction, liquid-liquid extraction, pervaporation and adsorption.

TABLE 3 PROPERTIES OF VARIOUS DOWNSTREAM PROCESSING TECHNIQUES [1, 12, 21, 24]

Gas Stripping

Principle Heating of effluent, purging with gas, condensation of solvent/water vapor

Liquid-liquid Extraction

Perstraction

Pervaporation

Adsorption

Contact with waterimmiscible solvent with fermentation broth, recovery of dissolved solvents by distillation Similar to liquid-liquid extraction, with a membrane separating fermentation broth and extractant Selective diffusion of solvents across a non-porous membrane, recovery of evaporated vapours by applying vacuum or sweep gas Adherence of solvents such as silicate or ion exchange resins, heat regeneration

Advantages Simple to perform, low chance of clogging or fouling, selectively removes volatile substances, reduce substrate inhibition, does not strip nutrients out or harm the cells High capacity, high selectivity, low chance of clogging or fouling, low energy requirement, does not strip nutrients out High selectivity, simple to perform

Disadvantages Does not remove solvents completely, more energy requirement compared to membrane-based process

Expensive to perform, possible forming of emulsions

Large membrane area required, possible clogging or fouling Lower membrane flux compared to membrane evaporation, possible clogging or fouling High price of material, low capacity, low selectivity, possible fouling

High selectivity compared to membrane evaporation, simple to perform

Lowest energy requirements of all the other methods

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Gas stripping is considered as the most economic and favorable option among all product recovery techniques due to its simplicity in operation [12]. In order to enhance the productivity, fed-batch fermentation is often incorporated with in-situ gas stripping by circulating nitrogen gas or fermentation gases (CO2 and H2) through the fermentation broth. It is normally initiated after a certain period after inoculation or right after the fermentation gases are produced at a rate of litre per min [25]. Butanol can be easily captured by the bubbled gas as it has lower vapor pressure in gas phase compared to the fluid phase. The solvents can be recovered from the gas by cooling it off in a condenser and condensed solvent will be collected in a receiver tank while the cleaned gas is recycled back to the fermentor. Gas stripping is continued until all fermentable sugars are utilized by the culture, or until there is a rapid decreased in productivity.

5 DISCUSSIONS
The availability of various type of agricultural crop for fermenting n-butanol was studied. The types and quantity of crops produced are heavily dependent on the cli-

mate of the country. Table 4 briefly summarizes the crop production in various countries for five commonly used substrates based on the statistics from Food and Agriculture Organization of the United Nation (FAO) in 2010 [26]. Over the years, Brazil is the largest producer of sugarcane, China for wheat, Midwest region of United States for corn, Nigeria for cassava, and Germany for barley. Large quantity of fibrous residues is produced from starch extraction and other industrial processes are treated as solid waste which to be disposed into landfills or used as low-value animal feed [12]. Thus, these agricultural wastes or lignocellulosic materials is said to have very low cost or almost zero value. The quantity of residue generated from the crop is estimated based on its residue-to-crop ratio. This ratio varies accordingly to various conditions during the growth of crops such as climate of grown area, fertilizer used and high yielding crops species. The selected values of ratio as shown in Table 4 are the average residue to crop production ratios for each type of crop. Factors such as climate, crop variety and differences in farming practice are included in consideration [27]. Based on the study of

TABLE 4 VARIOUS AGRICULTURAL CROPS AND ITS RESIDUE PRODUCTION IN 2010

Crop

Largest Producers
a

Crop Production
a

Worldwide Production
a

Residue-to-Crop Ratio
b

Rangeb

Residue Productione (million ton)

(million ton) Sugarcane Bagasse Brazil India China Wheat Straw China India United States Corn Stover United States China Brazil Cassava Bagasse Nigeria Brazil Indonesia Barley Straw Germany France Ukraine
aFood bYevich

(million ton) 1700 0.24 (240kg bagasse/ton of sugarcane) 654 1.30


c

717.5 292.3 111.5 115.2 80.8 60.1 316.2 177.5 55.4 37.5 24.5 23.9 10.4 10.1 0.8

172.2 70.2 26.8

0.9 1.6

149.8 105.0 78.1

840

2.0

0.9 4.0

632.4 355.0 110.8

230

0.93 (280 ton bagasse/300 ton of cassava)


d

34.9 22.8 22.2

1.60

1.4 2.0

16.6 16.2 1.3

and Agriculture Organization of the United Nation (2010) [26] & Logan(2003) [27] cDias et al.(2009) [15] dPandey, Soccol, Nigam, Soccol, Vandenberghe& Mohan (2000) [28] eCrop production multiply by residue-to-crop ratio

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Montano (2009), 1.4 million ton of wheat straw is required per annum for a biobutanol plant capacity of 100 kton/year biobutanol or 167 kton ABE/year [8]. It is shown that the residue generated by China, India, and United States have far more enough wheat straw to be utilized to produce biobutanol, at the same time able to protect the environment with proper waste disposal. In order to evaluate and compare the performance of various process experiments, control experiment is usually utilizing glucose as the pure substrate. A total of 17.6020.10g/L of ABE is produced in the batch reactors within fermentation period of 68-72 hours [16, 19, 22]. ABE productivity and yield of the control are 0.28-0.31g/L.h and 0.41g/g respectively. Various approaches of ABE fermentation were investigated and the results obtained from various researchers are listed in Table 5. The most common n-butanol producing culture used by the researchers is C.beijerinckii P260 and these results have proven that C.beijerinckii P260 has outstanding ability to convert biomass derived sugars (hydrolysates) into n-butanol [16]. It is noticed that wheat straw hydrolysate (WSH) fermentation can be fully consumed in a shorter period of 42 hours as compared to glucose fermentation that requires 72 hours. It is suggested that perhaps there are fermentation stimulatory components within WSH [19]. In addition, the results obtained from Qureshi et al. (2012) are having an ABE productivity of 0.60g/L.h, which has improved over 200% from the glucose fermentation [2]. Undiluted barley straw hydrolysate (BSH) fermentation is poor in comparison to WSH with productivity of 0.10g/L.h. The presence of inhibitory chemicals in BSH may have been the main reason for its poor performance. Thus, WSH is suggested to be more superior compared to BSH in ABE fermentation. On the other hand, cassava bagasse hydrolysate (CBH) undergone enzymatic hydrolysis has a productivity and yield of 0.62g/L.h and 0.39g/g respectively. CBH is suggested to be a suitable carbon source for ABE fermentation due to its high glucose content with little acids [12]. Sugar yield from pre-treatment and hydrolysis is strongly dependent on the composition of the biomass and types of pre-treatment. One gram of cassava bagasse which hydrolyzed by two-step enzymatic hydrolysis is able to produce 0.465g of sugars [12] whereas dilute acid and enzymatic hydrolysis of wheat straw is able to obtain 60.2g/L of sugars from 86g/L of substrate [16]. Total sugar yield of WSH is much higher, 0.7g/g of wheat straw compared to CBH, 0.465g/g of cassava bagasse. Inhibitors are the by-products obtained from pretreatment and hydrolysis. Table 6 and Fig. 3 show the presence of inhibitors and sugar degradation products in various untreated agricultural residue and energy crops hydrolysates. The concentration range of acetic acids, furfural, and HMF are 6.43-10.10g/L, 0.04-0.64g/L and 0.120.52g/L respectively. Among the four types of agricultural crops, wheat straw has the lowest by-product concentration. Unlike other lignocellulosic substrates, it was reported in recent studies that WSH does not required any

pre-treatment to remove inhibitors in order to be successfully fermented to n-butanol as fermentation of WSH was vigorous [2, 16]. Productivity of 0.60g/L.h of untreated WSH has proven that it does not inhibit the activity of the culture in the broth, including both cell growth and fermentation. In the undiluted BSH, ABE productivity is poor as there is no cell growth shown in the culture as a result of inhibition. In contrast, dilution of BSH with distilled water showed a significant improved in productivity (0.41g/L.h), which has improved 410% from the productivity of undiluted BSH (0.10g/L.h) and the yield improves from 0.33g/g to 0.39g/g [19]. On the other hand, corn stover hydrolysate (CSH) and switchgrass hydrolysate (SGH) shows a productivity of both 0.17g/L.h and yield of 0.43g/g and 0.39g/g respectively. The second approach of detoxification is known as overliming. The pH of the hydrolysate is needed to be adjusted to 10 with calcium hydroxide [Ca(OH)2]. A total of 26.64g/L ABE solvent is obtained from BSH with overliming approach with productivity and yield of 0.39g/L.h and 0.43 g/g respectively. High solvent production in the broth clearly proved that the inhibitors are removed successfully by overliming BSH. Similarly, overliming CSH is able to produced 26.27g/L of total ABE with productivity and yield of 0.31g/L.h and 0.44g/g respectively [9]. TABLE 6 PRESENCE OF INHIBITORS AND SUGAR DEGRADATION PRODUCTS IN VARIOUS UNTREATED AGRICULTURAL RESIDUE AND ENERGY CROPS HYDROLYSATES [19]

Substrate Wheat Straw Barley Straw Corn Stover Switchgrass

Acetic acid (g/L) 6.43 6.90 10.10 7.00

Furfural (g/L) 0.04 0.08 0.64 0.04

HMF (g/L) 0.12 0.16 0.52 0.48

Concentration (g/L)

0.8 0.6 0.4 0.2

Furfural

HMF

Fig. 3. Presence of inhibitors and sugar degradation products in


various untreated agricultural residue and energy crops hydrolysates [19]

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TABLE 5 SOLVENT PRODUCTION FROM GLUCOSE AND AGRICULTURAL RESIDUES IN BATCH AND FED-BATCH REACTORS
Substrate Strain Pretreatment/ Hydrolysis Treatment/ Product Recovery Gas stripping Simultaneous fermentation Simultaneous fermentation, gas stripping Undiluted Diluted with distilled water Overliming Diluted with distilled water Overliming Diluted with distilled water Overliming + XAD-4 Fermentation Time (h) Initial Substrate (g/L) 62.0 58.3 60.2 25.4 25.6 26.1 Substrate Utilized (g/L) 48.9 51.4 45.4 59.3 25.4 25.6 26.1 ABE (g/L) Acetone (g/L) Butanol (g/L) ABE Productivity (g/L.h) 0.28 0.31 0.29 0.60 0.60 0.19 0.27 0.31 ABE Yield (g/g) 0.41 0.41 0.39 0.47 0.42 0.37 0.42 0.41 Reference

Batch Fermentation Glucose Glucose Glucose Glucose Wheat straw Wheat straw Wheat straw Wheat straw

C.beijerinckiiP260 C.beijerinckiiP260 C.beijerinckiiBA101 C.beijerinckiiBA101 C.beijerinckiiBA101 C.beijerinckiiP260 C.beijerinckiiP260 C.beijerinckiiP260

Dilute acid Dilute acid Dilute acid + enzyme Dilute acid + enzyme Dilute acid Dilute acid Dilute acid Dilute acid Dilute acid Dilute acid Dilute acid + enzyme Enzyme

72 68 42 50 45 71

20.10 21.06 17.60 75.90 25.00 9.36 11.93 21.42

6.70 5.44 27.40 11.90 2.72 3.74 -

12.70 15.21 46.4 12.00 6.05 7.40 -

Qureshi et al. (2007) Qureshi et al. (2009a) Ezeji et al. (2004) Lu et al. (2011) Qureshi et al. (2012) Qureshi et al. (2007a) Qureshi et al. (2007a) Qureshi et al. (2007a)

[16] [19] [22] [12] [2] [17] [17] [17]

Barley straw Barley straw Barley straw Corn stover Corn stover Switch grass Corn fibre Cassava bagasse +glucose

C.beijerinckiiP260 C.beijerinckiiP260 C.beijerinckiiP260 C.beijerinckiiP260 C.beijerinckiiP260 C.beijerinckiiP260 C.beijerinckiiBA101 C. acetobutylicum JB200

68 42 68 96 85 84 55

58.8 59.0 63.4 60.0 60.3 58.9 -

21.8 44.5 62.3 37.3 59.8 86.2

7.09 17.42 26.64 16.00 26.27 14.61 9.30 33.87

6.93 4.70 8.00 4.35 5.30 10.20

18.01 10.40 14.50 9.55 11.90 20.32

0.10 0.41 0.39 0.17 0.31 0.17 0.10 0.62

0.33 0.39 0.43 0.43 0.44 0.39 0.39 0.39

Qureshi et al. (2009a) Qureshi et al. (2009a) Qureshi et al. (2009a) Qureshi et al. (2009b) Qureshi et al. (2009b) Qureshi et al. (2009b) Ezeji, T. & Blaschek, H. (2008) Lu et al. (2011)

[19] [19] [19] [9] [9] [9] [29] [12]

Fed-batch Fermentation Glucose C.beijerinckiiBA101 Cassava bagasse C. acetobutylicum JB200 Cassava bagasse C. acetobutylicum JB200 Wheat straw + C.beijerinckiiP260 glucose Wheat straw C.beijerinckiiP260

Dilute acid Dilute acid Dilute acid Dilute acid

Gas stripping Gas stripping Gas stripping Overliming, gas stripping Simultaneous Fermentation, gas stripping

201 169 263 533

433.9

500.0 244.6 336.6 430.0

232.80 90.31 108.50 47.60 192.00

77.70 25.72 26.98 -

151.70 59.81 76.44 -

1.16 0.53 0.41 0.36 0.36

0.47 0.37 0.32 0.37 0.44

Ezeji et al. (2004) Lu et al. (2011) Lu et al. (2011) Qureshi et al. (2007) Qureshi et al. (2007b)

[22] [12] [12] [16] [25]

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Fig. 4. Simplified process flow diagram for overall biobutanol production [2, 9, 17, 19, 24, 25]

Fermentation is stopped due to deficiency of sugars when the substrate has completely utilized all fermentable sugars in the broth (residual sugar = 0g/L) [17]. When sugar utilization is faster than hydrolysis, the culture might be affected negatively and thus reducing system productivity. Therefore, fed-batch system is recommended where sugar solution is fed at a slow rate into the broth to enable continuous sugar utilization. Based on the research in Ezeji et al. (2004), the control experiment in a fed-batch reactor utilizing glucose produced a total ABE of 232.8g/L in 201 hours [22]. The ABE productivity and yield are 1.16g/L.h and 0.47g/g respectively. In comparison with batch fermentation (0.29g/L.h), fed-batch fermentation is able to improve the productivity up to 400%. Unlike batch system, fed-batch system is running in longer period in order to hydrolyze the substrate completely. Fed-batch fermentation integrated with in-situ gas stripping is more superior to the batch fermentation in overall ABE production due to simultaneous product removal that can maintain its toxicity at low level. The control experiment in batch reactor with gas stripping results in a productivity of 0.60g/L.h and yield of 0.47g/g, with a total solvent production of 75.90g/L [12]. The solvent production has significantly enhanced by the effect of gas stripping at a minimum of 3.6 fold (21.06g/L in control batch reactor without gas stripping). Continuous gas stripping allows n-butanol concentration to maintain below the toxic level as it preferentially removes n-butanol over acetone from the fermentation broth. As reported by Lu et al. (2011), typical production ratio of n-butanol to acetone in batch fermentation is 2:1 whereas butanol to acetone ratio for fed-batch system with integrated gas stripping has a significant increased to greater than two (2.33-2.84) [12]. This system can effectively produces large quantity of ABE (90.31-108.5g/L), at the same time able to keep the solvent concentration at almost the same concentration of ~10g/L in the broth. Fig. 4 shows a simplified process flow diagram for the overall biobutanol production. It is a conceptual design de-

veloped based on the research results of various studies. Agricultural residue is first milled into smaller particle size before being fed into the pre-treatment tank. Dilute H2SO4 is added for pre-treatment and Ca(OH)2 will be added in the mixing tank for overliming to remove the inhibitors. This process is having simultaneous hydrolysis and fermentation with agitation by gas stripping in a fed-batch reactor. This system is developed by Qureshi et al. (2007b) with the main objective to economize the production of n-butanol by combining hydrolysis and fermentation process integrated with product recovery in a single step [25]. At the time of inoculation, three hydrolytic enzymes are required to be added together into the reactor. Agitation of fermentation broth for nbutanol recovery can be performed by circulating CO2 and H2 gases produced during fermentation. At the same time, a more concentrated sugar solution is fed into the fermentor at a slow rate to establish fed-batch fermentation. In batch reactor, as compared to conventional approach, the ABE production from WSH has increased from 9.36g/L to 11.93g/L, shows a significant improvement of 27% as shown in Table 5. ABE production further increased to 21.42g/L when the simultaneous hydrolysis and fermentation is integrated with gas stripping, with productivity and yield of 0.31g/L.h and 0.41 g/g respectively. On the other hand, ABE productivity is enhanced to about 16%, from 0.31g/L.h in batch system to 0.36g/L.h in fed-batch system. ABE production in this fed-batch system is 192g/L, very much close to control experiment utilizing glucose (232.8g/L), and results in a much higher production compared to conventional approach. Thus, this study concluded that WSH is hydrolyzed completely and made simultaneous hydrolysis and fermentation a successful process. After fermentation, the downstream processing design is adopted from the study of Merwe et al. (2012) [24]. Among several process designs being investigated, it is reported that this process design is considered to be in favorable energy performance position as liquid-liquid extraction has high performance with low energy requirement.

15

CONCLUSION
[8] [9]

In this study, the overall production techniques of biobutanol were studied. Biobutanol has proven to be a superior biofuel as compared to ethanol due to its more favorable physical and chemical properties. Utilization of lignocellulosic substrates such as wheat straw, barley straw, sugarcane bagasse, cassava bagasse and etc is the current trend in biobutanol production due to its low cost and wide availability. Among all, wheat straw is an effective substrate in ABE production and does not required any pretreatment of inhibitors, with an average productivity and yield of 0.36g/L.h and 0.44g/g respectively. C. beijerinckii P260 is a good strain in converting biomass into fermentable sugars. Further improvement in productivity can be done in fed-batch system integrated with gas stripping. In addition, simultaneous hydrolysis and fermentation is able to further enhance the efficiency of the system, at the same time greatly reduce the cost of production.

[10] [11]

[12]

[13] [14]

[15]

FUTURE WORK AND CHALLENGES


[16]

In future study, optimization of the developed process design in simultaneous hydrolysis and fermentation will be carried out by conducting more experiments and simulations by using sugarcane bagasse as fermentation substrates in the collaboration with industrial and agricultural estate such as sugarcane plantation in Australia, as well as to perform a detailed economic assessment on the overall biobutanol production. Current technology involved in the production of biobutanol as biofuel is still immature. Most of the research is still proceeding in laboratory-scale.

[17]

[18] [19]

REFERENCES
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Neo Lei Yee is current a final year chemical engineering student of Universiti Tunku Abdul Rahman, Kuala Lumpur, Malaysia. She had her earlier education in Sekolah Menengah Kebangsaan Taman Connaught, Kuala Lumpur, Malaysia. She holds student membership of Institute of Engineer Malaysia and Institute of Chemical Engineer, Malaysia. Her academic achievement has earned her to be listed in President and Dean honor-list consecutively for year 2009-2012. She had participated and won prizes in a number of national level Chemical Engineering Design competitions. Lim Soo King obtained his BSc(Hons) degree from University of London in 1979, MSc degree from University of Malaya in 1993, and PhD degree from University of Malaya in 2000. He started his first employment in Malaysia with Semiconductor Division of Harris Corporation, Florida, USA. His last position with the company was an Engineering Manager. In year 2004, he joined Universiti Tunku Abdul Rahman as an associate professor. In his last nine years of employment with Universiti Tunku Abdul Rahman, he had held several key management positions including chairperson of a research centre and Dean of a Faculty. He has actively involved in research publication. To date he has authored and co-authored more than 30 conference proceedings and journal papers. He had sat in a number of conference committees as paper reviewer and conference session chairperson. He is an active consultant for semiconductor industry in Malaysia. Low Chong Yu is currently an assistant professor with the Faculty of Engineering & Green Technology, Universiti Tunku Abdul Rahman, Perak, Malaysia. He has more than 28 years of working experience in process equipment & plant design, and troubleshooting of simulation systems for the petrochemical industries in Singapore & Malaysia. He earned his BSc in chemical engineering from National Taiwan University in 1974. He obtained his MSc degree in petrochemical & hydrocarbon chemistry and PhD degree in chemical engineering respectively in 1976 and in 1979 from the University of Manchester, England. He has postgraduate qualifications in process equipment design with international standard codes, process simulation with Hysys system analysis, management consulting and training. He is a professional engineer registered with the Board of Engineers, Malaysia. His consulting work include oil & gas and petrochemical industries in the areas of corporate development and knowledge models for process & petrochemical plants development to address decision-making needs. His research interest includes ethanol or butanol blended with gasoline as a biofuel from different types of agricultural sources.

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