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PEER-REVIEWEDAssessment Evaluation of Bio-Ethanol Yield for Energizing Prosthetics Production Plant Based on Bacterial Growth and Shaking Rate
C. I. Nwoye1,
, P. C. Agu2, B. C. Chukwudi3, S. O. Nwakpa1, I. A. Ijomah1, N. E. Idenyi4
1Department of Metallurgical and Materials Engineering, Nnamdi Azikiwe University, Awka, Nigeria
2Department of Metallurgical and Materials Engineering, Federal University of Technology, Owerri, Nigeria
3Department of Mechanical Engineering, Imo State University, Owerri, Nigeria
4Department of Industrial Physics, Ebonyi State University, Abakiliki, Nigeria
Abstract
This paper presents an assessment evaluation of bio-ethanol yield based on the bacteria growth (BG) and shaking rate (SR) during bioprocessing of sugar cane molasses with Saccharomyces cerevisiae. Critical computational analysis of generated experimental results indicates that the bio-ethanol yield response typified an empirical model which is exponential-linear in nature. The model was validated prior to evaluation of the yield response coefficient and predictive analysis of generated results. The validity of the derived model expressed as; ζ = 4.6335e[0.0068(ϑ/ɤ)] + 0.00012₰ - 0.00004ε was rooted on the core model expression ζ - 0.00012 ₰ = 4.6335e 0.0068(ϑ/ɤ) - 0.00004ε where both sides of the expression are correspondingly approximately equal. Results of ethanol yield were generated using regression model and its trend of distribution was compared with that from derived model for the purpose of verifying its validity relative to experimental results. The results of the verification process show very close dimensions of covered areas and alignment of curves designating ethanol yield, which precisely translated into significantly similar trend of data point’s distribution for experimental (ExD), derived model (MoD) and regression model-predicted (ReG) results. Ethanol yield per unit input ratio SR/ BG were evaluated from experimental, derived model & regression model predicted results as 0.0496, 0.0573 & 0.0565 rpm/ O.D respectively. Standard errors incurred in predicting ethanol yield for each value of SR, BG & SR/ BG considered as obtained from experiment, derived model and regression model were 0.13369, 0.9674 and 1.3380%, 1.3096, 1.3615 and 1.5300 % & 1.3701, 0.5969 and 1.1459 x 10-5 respectively. The operationally viable deviation range of model-predicted ethanol yield from the experimental results was 0.9 -13.47 %. This translated into 86.53-99.1 % operational confidence and reliability level for the derived models, as well as 0.86 - 0.99 yield response coefficient of ethanol to the input ratio SR/ BG. Consequently, in order to obtain high confidence level, the derived model considers input parameter value; 50 rpm (shaking rate) very extraneous. This was as a result of 23.66% deviation associating the use of this input parameter value.
Keywords: Bio-Ethanol yield, input ratio of shaking rate and microbial growth, bioprocessing sugar cane molasses, Saccharomyces cerevisiae
Received August 17, 2014; Revised October 25, 2014; Accepted June 25, 2015
Copyright © 2015 Science and Education Publishing. All Rights Reserved.Cite this article:
- C. I. Nwoye, P. C. Agu, B. C. Chukwudi, S. O. Nwakpa, I. A. Ijomah, N. E. Idenyi. Assessment Evaluation of Bio-Ethanol Yield for Energizing Prosthetics Production Plant Based on Bacterial Growth and Shaking Rate. Biomedical Science and Engineering. Vol. 3, No. 1, 2015, pp 15-22. https://pubs.sciepub.com/bse/3/1/4
- Nwoye, C. I., et al. "Assessment Evaluation of Bio-Ethanol Yield for Energizing Prosthetics Production Plant Based on Bacterial Growth and Shaking Rate." Biomedical Science and Engineering 3.1 (2015): 15-22.
- Nwoye, C. I. , Agu, P. C. , Chukwudi, B. C. , Nwakpa, S. O. , Ijomah, I. A. , & Idenyi, N. E. (2015). Assessment Evaluation of Bio-Ethanol Yield for Energizing Prosthetics Production Plant Based on Bacterial Growth and Shaking Rate. Biomedical Science and Engineering, 3(1), 15-22.
- Nwoye, C. I., P. C. Agu, B. C. Chukwudi, S. O. Nwakpa, I. A. Ijomah, and N. E. Idenyi. "Assessment Evaluation of Bio-Ethanol Yield for Energizing Prosthetics Production Plant Based on Bacterial Growth and Shaking Rate." Biomedical Science and Engineering 3, no. 1 (2015): 15-22.
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At a glance: Figures
1. Introduction
The renewed growing need and demand for a cheap fuel, usable in the transportation system; for conveying goods and services as well as running industrial machines has resulted to successful processing and usage of agricultural products, such as cassava and molasses, for ethanol production which is 99.5% pure alcohol by volume [1]. Ethanol production from agro-products and wastes was also anchored on the fact that increased fossil-fuel demand, due to the increased global energy consumption, and the attendant limitations of fossil carbon reservoir compelled human beings to consider alternative energy source, biofuel which is renewable and produced with quasi-zero Co2 [2].
Reported has shown [3] that the vast majority of ethanol for use as fuel, is produced by fermentation: when certain species of yeast (such as Saccharomyces cerevisiae) metabolize sugar in the absence of oxygen, they produce ethanol and carbon dioxide. The overall chemical reaction conducted by the yeast may be represented by the chemical equation
 | (1) |
The researcher [3] showed that a fermenting strain of Saccharomyces cerevisiae could be utilized for alcoholic fermentation using sugarcane molasses. The scientist optimized fermentation of molasses with respect to temperature, pH and sugar concentration. Results of the process revealed a temperature of 30°C, pH 6.0 and 20% sugar concentration as optimum for fermentation. Under optimized conditions, S.cerevisiae produced 11.6% of ethanol. Immobilization resulted in 10.4% ethanol after 48 hours and the same yeast cells were reused to carry out fermentation. The reuse of immobilized cells gave 7.9% ethanol yield. Ethanol production capacity of novel Xylose-fermenting yeast, Scheffersomyces shehatae UFMG-HM52.2 was evaluated under batch fermentation conditions using sugarcane bagasse hemicellulosic hydrolysate as carbon source and found very laudable and recommendable [4]
Alcoholic fermentation has been carried out using a number of sugary materials depending upon their availability and suitability in particular geographic situations. Various raw materials like sugarcane juice and molasses [5, 6] sugar beet, beet molasses [6, 7], Sweet sorghum [8] and starchy materials like sweet potato [9] Corn cobs and hull [10, 11], cellulosic materials like cocoa, pineapples and sugarcane waste [12] and milk/cheese/whey using lactose hydrolyzing fermenting strains [13, 14] have been reported. Amongst these, simple sugar bearing materials are the easiest to process, since the yeast ferment these directly while other carbohydrates like starch/cellulose have to be first hydrolyzed to fermentable sugars using current and sound commercial technologies (physio-chemical/enzymatic preparation) before they can be fermented to yield ethanol.
Studies [15] show that ethanol production from wheat starch. Hydrolyzed wheat starch was used as a substrate for ethanol production using 2 strains of S.cerevisiae. Wheat flour slurry (25%w/v) was gelatinized and conditions were standardized for saccharification and fermentation of wheat starch for ethanol production.
Ethanol in India and other developing countries is mainly produced by fermentation of dilute molasses at ambient temperature of 25-35oC employing Saccharomyces cerevisiae [8, 16].
A researcher [17] studied the effect of pretreatment of sugarcane molasses for ethanol production by yeast. The effect of pretreatment of molasses with H2SO4 and K4Fe(CN)6 on ethanol production by different yeast strain was studied in order to find an effective method to reduce the load of various inhibitory substances and to select a suitable yeast strain for fermentation of pretreated molasses. Pretreatment resulted in decreased level of inhibitory substances like Ca, Cu, and Fe in the molasses solution with improved ethanol production. The inhibitory effect of these constituents was confirmed by supplementation of synthetic medium with residues from different pretreatments and the inhibitory level for various constituents was found to be Ca>0.5%, iron> 46ppm and Cu >5.4ppm. The fermentable carbohydrates in molasses are sucrose and other sugars mainly glucose and fructose.
In fermentation of the various ethanol producing micro-organism yeast belonging to Saccharomyces cerevisiae have been used most commonly. Scientists [18] have isolated yeast from spoiled high sugar foods. Another scientist [19] compared the rates of growth and ethanol production by 11 different strains of Zymomonas, with some strains being more tolerant of high sugar or ethanol concentration and high incubation temperature than others. One of the most promising ethanol producing organisms is the bacterium Zymomonas mobilis which is used to make palm wines. This bacterium can produce upto 1.9 mol of ethanol from each mole of glucose fermented.
Following a comparative study [20] carried out on ethanol production from molasses using Saccharomyces cerevisiae & Zymomonas mobilis, yeast was found to be more ethanol tolerant and produced more ethanol at sugar concentration above 15% (v/v).
A yeast, S. cerevisiae was also isolated [21] from palm wine, which produced increased amounts of ethanol in yeast extract peptone dextrose medium. Later research [22] revealed isolation of new strains of S.cerevisiae on basal medium containing 48% sucrose from fermenting sample collected from Brazilian alcohol factories. Isolated strains fermented concentrated sugarcane syrups as well as high sucrose solution in synthetic medium with conversion efficiency of 89-92%.
Fermentation efficiencies less than 90% are quite common though it should be 95% on an average. Secondly, exact conditions of temperature, pH and nutrients, which are essential for yeast fermentation, are not vigorously maintained.
An empirical model was derived [23] for assessment evaluation of the concentration of ethanol yield during microbial treatment of sugar cane molasses. The model expressed as;
 | (2) |
shows that the concentration of ethanol produced during the bio-treatment process is dependent on the inoculums size and the growth of microbes attacking the substrate. Ethanol productions per unit inoculums size and microbial growth are -1.86% / O.D and -1.6397% / O.D & - 4.5146 and –3.9798 % (O.D)-1 as obtained from experiment & derived model respectively. Statistical analysis of the results indicate that the variance and standard deviation as obtained from experiment and derived model are 5.2674 and 2.2951 as well as 4.8777 and 2.2086 respectively, indicating proximate agreement. Deviational analysis indicates that the maximum deviation of the model-predicted ethanol yield from the corresponding experimental value is less than 14%. The validity of the model was found to be rooted on the expression 0.204 y = 0.1634 γ3 – γ2 + 1.5584 γ – 1.4039 β2 + 3.1898 β – 0.1655 where both sides of the expression are correspondingly approximately almost equal. Optimization of ethanol production was based on variation in microbial growth while the inoculum size and all other process parameters were assumed constant. The optimization model; y = 31.272β – 13.763β2 – 5.9758 which was constituted by only the parameter for microbial growth indicates that the optimum ethanol production; 13.9198% would be obtained at an optimum microbial growth of 1.1361 (O.D). The validity of the optimization model was found to be rooted on the expression equations 0.1673 y + 1 = 5.2331 β – 2.3031 β2.
An empirical model [24] was successfully derived for predictive analysis of the concentration of ethanol yield during bio-treatment of sugar cane molasses. The model expressed as;
 | (3) |
shows that the concentration of ethanol produced during the bio-treatment process is dependent on the shaking rate of the reaction vessel and the growth of microbes attacking the substrate. Ethanol production per unit shaking rate are 0.0320 and 0.0391 % (rpm)-1 as obtained from experiment and derived model respectively. Similarly, ethanol production per unit growth of microbes are 7.1429 and 8.7290 % (O.D)-1 as obtained from experiment and derived model respectively. Statistical analysis of the results indicate that the variance and standard deviation as obtained from experiment and derived model are 10.1588 and 3.1873 as well as 11.6728 and 3.4166 respectively, indicating proximate agreement. The validity of the model was found to be rooted on the expression 0.1090 β – 0.0985 = 0.0037α – 5.45 x 10-6 α2 + γ - 0.2912 γ2 where both sides of the expression are correspondingly approximately almost equal. Optimization of ethanol production was based on variation in shaking rate only while the microbial growth and all other process parameters were assumed constant. The optimization model; β = 0.0684 α – 0.0001 α2 + 4.3607 which was constituted by only the shaking rate parameter indicates that the optimum ethanol production; 16.0571% would be obtained at an optimum shaking rate of 342 rpm. The validity of the optimization model was found to be rooted on the expression 0.2293 β -1 = 0.0157 α – 2.29 x 10-5 α2.
Successful analysis and prediction of ethanol yield was carried out [25] during biodegradation of sugar cane molasses. Validity of the derived model expressed as;
 | (4) |
was rooted on the expression 0.3372 (α + 35.8547) = 1.8292 ln β – 0.0161 γ2 + γ where both sides of the expression are correspondingly approximately equal. The model shows the dependency of produced ethanol on the treatment temperature and the growth of microbes attacking the substrate. Ethanol yield per unit temperature rise during the process are 15.3889 and 17.3578% / 0C as obtained from experiment and derived model respectively. Similarly, ethanol production per unit growth of microbes are – 0.1847 and – 0.2083 % (O.D)-1 as obtained from experiment and derived model respectively. Statistical analysis of the results indicate that the variance and standard deviation as obtained from experiment and derived model are 8.1440 and 2.8538 as well as 7.4053 and 2.7213 respectively, indicating proximate agreement.
The present work aims at taking an assessment evaluation of bio-ethanol yield (for energizing prosthetics production plant) based on the input ratio of shaking rate and microbial growth during bioprocessing of sugar cane molasses with Saccharomyces cerevisiae. [1] reported that the produced bio-ethanol is cheap; 99.5% pure and applicable for running industrial machines such as machines for prosthetics production. Therefore this work shows the relationship between the biofuel yield (which are supplied directly to the prosthetics plant) and the process inputs: bacterial growth and shaking rate of reaction vessel affecting the yield.
2. Materials and Methods
A weighed quantity of prepared sugar cane molasses was put in a reaction vessel containing the appropriate Saccharomyces cerevisiae. Details of the experimental procedure and associated process conditions are as stated in the past report [1]. Analysis of the bio-ethanol production was carried out based on the input ratio of shaking rate and microbial growth using a derived and validated empirical model.
2.1. Model FormulationExperimental data obtained from research work [1] were used for this work. Computational analysis of the data [1] shown in Table 1, gave rise to Table 2 which indicate that;
 | (5) |
Introducing the values of S, K and N into equation (5) reduces it to;
 | (6) |
 | (7) |
S = 0.00012, K = 0.0068, N = 4.6335 and Se = 0.00004 are empirical constants (determined using C-NIKBRAN [26].
Where
(ϑ) = Shaking rate (SR) (rpm)
(ɤ) = Microbial growth (BG)
(ζ) = Ethanol yield conc. (%)
(ϑ/ɤ)= input ratio SR/ BG
(₰ ) = Treatment temperature (0C)
(ε) = Reaction time (hrs)
Table 1. Variation of ethanol yield concentration with shaking rate (SR), microbial growth (BG) and input ratio SR/ BG [1]
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3. Boundary and Initial Condition
Consider sugar cane molasses interacting with microbes. The atmosphere in the reaction vessel was not contaminated i.e (free of unwanted gases and dusts). Range of shaking rate, microbial growth and input ratio SR/ BG used: 0-250 rpm, 0.43-1.55 and 0 – 161.2903 respectively. Furthermore, reaction time and treatment temperature used maintained constant as 72hrs and 30°C respectively. Mass of wastes used and other process conditions are as stated in the experimental technique [1].
The prevailed boundary conditions are: anaerobic atmosphere to enhance microbial action on the sugar cane molasses. At the bottom of the particles, a zero gradient for the gas scalar are assumed and also for the gas phase at the top of the waste particles. The biodegraded waste was stationary. The sides of the waste particles are taken to be symmetries.
4. Results and Discussion
4.1. Model ValidationEquation (7) is the derived model.
The validity of the model is strongly rooted on equation (5) where both sides of the equation are correspondingly approximately equal. Table 2 also agrees with equation (5) following the values of ζ - 0.00012 ₰ and 4.6335e0.0068(ϑ/ɤ) - 0.00004ε which were precisely evaluated from the experimental results in Table 1. Furthermore, the derived model was validated by comparing the ethanol yield predicted by the model and that obtained from the experiment [1]. This was done using the 4th Degree Model Validity Test Techniques (4th DMVTT); computational, graphical, statistical and deviational analysis [27].
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Statistical Analysis
Standard Error (STEYX)
The standard errors incurred in predicting ethanol yield for each value of SR, BG & SR/BG considered as obtained from experiment and derived model were 1.3369, 1.3096 & 1.3701% and 0.9674, 1.3615 & 0.5969 % respectively. The standard error was evaluated using Microsoft Excel version 2003.
Correlation (CORREL)
The correlation coefficient between ethanol yield and SR, BG & SR/BG were evaluated (using Microsoft Excel Version 2003) from results of the experiment and derived model. These evaluations were based on the coefficients of determination R2 shown in Figure 1-Figure 6.
 | (8) |
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The evaluated correlations are shown in Tables 3-5. These evaluated results indicate that the derived model predictions are significantly reliable and hence valid considering its proximate agreement with results from actual experiment.
Table 3. Comparison of the correlations evaluated from derived model predicted and experimental results based on shaking rate
Table 4. Comparison of the correlations evaluated from derived model predicted and experimental results based on microbial growth
Table 5. Comparison of the correlations evaluated from derived model predicted and experimental results based on input ratio SR/ BG
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Graphical Analysis
Comparative graphical analysis of Figure 7-Figure 9 show very close alignment of the curves and shapes from the experimental (ExD) and model-predicted (MoD) ethanol yields. Furthermore, the degree of alignment of these curves is indicative of the proximate agreement between both experimental and model-predicted ethanol yields.
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Comparison of derived model with standard model
The validity of the derived model was also verified through application of the regression model (Reg) (Least Square Method using Excel version 2003) in predicting the trend of the experimental results. Comparative analysis of Figure 10-Figure 12 shows very close dimensions of aligned areas covered by ethanol yield, which precisely translated into significantly similar trend of data point’s distribution for experimental (ExD), derived model (MoD) and regression model-predicted (ReG) results of ethanol yield.
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Also, the calculated correlations (from Figure 10-Figure 12) between ethanol yield and SR, BG & SR/BG for results obtained from regression model were 0.8750, 0.8641 & 0.9878 respectively. These values are in proximate agreement with both experimental and derived model-predicted results. The standard errors incurred in predicting ethanol yield for each value of SR, BG & SR/BG considered as obtained from regression model were 1.3380, 1.53 & 3.1459 x 10-5 % respectively.
Computational Analysis
Critical computational analysis of the experimental and model-predicted ethanol yield was carried out to ascertain the degree of validity of the derived model. This was done by comparing results of evaluated ethanol yield per unit value of input ratio SR/ BG as obtained from experimental and derived model within shaking rate and microbial growth range: 0-250 rpm and 0.43 – 1.55 O.D respectively.
Ethanol yield per unit SR /BG ratio ζ / (ϑ /ɤ) (rpm/O.D) was calculated from the equation;
 | (9) |
Re-written as
 | (10) |
Equation (10) is detailed as
 | (11) |
Where
Δζ = Change in the ethanol yield ζ 2, ζ 1 at two values of SR/ BG ratios (ϑ /ɤ)2 , (ϑ /ɤ)1.
Considering the points (0, 4.93) & (161.2903, 12.93), (0, 4.6335) & (161.2903, 13.875) and (0, 4.1491) & (161.2903, 13.2548) as shown in Table 1 and Figure 12, then designating them as (ζ1, (ϑ /ɤ) 1) & (ζ2, (ϑ /ɤ) 2) for experimental, derived model and regression model predicted results respectively, and then substituting them into equation (11), gives the slopes: 0.0496, 0.0573 and 0.0565 (rpm/O.D) respectively as their corresponding ethanol yield per unit input ratio SR/ BG.
The proximity between these values indicates significantly high validity level for the derived model.
Deviational Analysis
Critical analysis of the ethanol yields precisely obtained from experiment [1] and derived model shows deviations on the part of the model-predicted values relative to values obtained from the experiment. This is attributed to the fact that surface properties of the sugar cane molasses and the physico-chemical interactions between the molasses and the infesting microbes which played vital roles during the biofuel production process [1] were not considered during the model formulation. This necessitated the introduction of correction factor, to bring the model-predicted ethanol yield to those of the corresponding experimental values.
The deviation Dv, of model-predicted ethanol yield from the corresponding experimental result was given by
 | (12) |
Where
ζExD and ζMoD are ethanol yield evaluated from experiment and derived model respectively.
The correction factor took care of the negligence of operational contributions of surface properties of the sugar cane molasses and the physico-chemical interactions between the cane molasses and infesting microbes which actually played vital role during the ethanol production process. The model predicted results deviated from those of the experiment because these contributions were not considered during the model formulation. Introduction of the corresponding values of Cf from equation (11) into the model gives exactly the corresponding experimental ethanol yield.
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Deviational analysis of Table 6 relative to input ratio SR/BG indicates that the operationally viable deviation range of model-predicted ethanol yield from the experimental results is 0.9-13.47 %. This invariably translated into 86.53-99.1 % operational confidence and reliability level for the derived models as well as 0.86-0.99 reliability coefficient for the yield response of ethanol to input ratio SR/ BG.
Consequently, in order to obtain high confidence level, the derived model considers input parameter value; 50 rpm (shaking rate) very extraneous. This was as a result of 23.66% deviation associating the use of this input parameter value.
Consideration of equation (12) and critical analysis of Table 6 and Figure 12 indicate that the highlighted deviation range corresponds to ethanol yields: 11.6140 - 11.2058 % and input ratio SR/BG:135.1351-129.8701 rpm/ O.D respectively.
Correction factor, Cf to the model-predicted results was given by
 | (13) |
Critical analysis of Table 6 indicates that the evaluated correction factors are negative of the deviation as shown in equations (12) and (13). Table 6 shows that the operationally viable range of correction factors to the model-predicted methane gas yield were – 0.9 to + 13.47 %. Table 6 and Figure 12 indicate that these highlighted correction factors correspond to ethanol yields: 11.6140-11.2058 % and input ratio SR/BG: 135.1351-129.8701 rpm/ O.D respectively.
It is important to state that the deviation of model predicted results from that of the experiment is just the magnitude of the value. The associated sign preceding the value signifies that the deviation is a deficit (negative sign) or surplus (positive sign).
5. Conclusion
Ethanol yield response was evaluated based on the operational input ratio of shaking rate (SR) and microbial growth (BG) during bioprocessing of sugar cane molasses with Saccharomyces cerevisiae. Ethanol yield response typified an empirical model which is exponential-linear in nature. The validity of the derived model was rooted on the core model expression ζ - 0.00012 ₰ = 4.6335e 0.0068(ϑ/ɤ) - 0.00004ε where both sides of the expression are correspondingly approximately equal. Ethanol yield per unit input ratio SR/ BG were evaluated from experimental, derived model & regression model predicted results as 0.0496, 0.0573 & 0.0565 rpm/ O.D respectively. Standard errors incurred in predicting ethanol yield for each value of SR, BG & SR/ BG considered as obtained from experiment, derived model and regression model were 0.13369, 0.9674 and 1.3380%, 1.3096, 1.3615 and 1.5300 % & 1.3701, 0.5969 and 1.1459 x 10-5 respectively. The operationally viable deviation range of model-predicted ethanol yield from the experimental results was 0.9 -13.47 %. This translated into 86.53-99.1 % operational confidence and reliability level for the derived models, as well as 0.86 - 0.99 yield response coefficient of ethanol to the input ratio SR/ BG. Consequently, in order to obtain high confidence level, the derived model considers input parameter value; 50 rpm (shaking rate) very extraneous. This was as a result of 23.66% deviation associating the use of this input parameter value.
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