Spirogyra Oil-Based Biodiesel: Response Surface Optimization of Chemical and Enzymatic Transesteriﬁcation and Exhaust Emission Behavior

: Algae are emerging as a major and reliable source of renewable biodiesel that could meet the energy requirements of the world. Like plants, algae produce and store oils in their cells. Algal samples were collected from Gujrat District, Pakistan, their oil content was analyzed, and the best oil producing alga was identiﬁed as Spirogyra crassa . After collecting sample, oil was extracted using the Soxhlet extraction method. Spirogyra oil was characterized physico-chemically for the evaluation of its quality. Acid value, density, saponiﬁcation value, peroxide value, as well as viscosity and iodine values were determined and their values were 16.67 ± 3.53 mg KOH / g, 0.859 ± 0.050 g / cm 3 , 165.33 ± 13.20 mg KOH / g, 4.633 ± 0.252 meq / kg, 5.63 ± 0.833 mm 2 / mL, and 117.67 ± 13.01 mg I 2 / g, respectively. Chemical as well as enzymatic transesteriﬁcation protocols were employed for biodiesel production using NaOCH 3 and NOVOZYME-435, respectively. Di ﬀ erent reactions parameters involved in transesteriﬁcation were optimized by the response surface methodology. The optimized yield of biodiesel (77.3 ± 1.27%) by the chemical transesteriﬁcation of algal oil (spirogyra) was observed by carrying out the reaction for 90 minutes at a reaction temperature of 45 ◦ C using 1.13% catalyst (NaOCH 3 ) concentration and 6:1 methanol:oil. Meanwhile, for enzymatic transesteriﬁcation, the optimized yield (93.2 ± 1.27%) was obtained by conducting the reaction for 42.5 h at the temperature of 35 ◦ C using 1% enzyme concentration and 4.5:1 methanol:oil. Fuel properties, including ﬂash point, pour point, cloud point, ﬁre point, kinematic viscosity, and density, were determined and their values are 125.67 ± 2.11 ◦ C, − 19.67 ± 0.8 ◦ C, − 13 ± 1 ◦ C, 138.667 ± 2.52 ◦ C, 5.87 ± 2.20 mm 2 / mL, and 0.85 6 ± 0.03 g / cm 3 , respectively. Fourier transfer infrared spectroscopic (FTIR) and Gas chromatography with ﬂame ionization detector (GC-FID) analysis were performed for the monitoring of the transesteriﬁcation process and fatty acid methyl acid (FAME) proﬁling, respectively.


Introduction
Energy is a vital necessity for growth and economic development in every sector of life, such as transportation, industrial unit and agriculture [1]. The requirement of energy is increasing day by day owing to the expansion of the population and spread of industries throughout the world to meet the requirements of an expanding human pollution. The world largely depends on fossil fuels which are nonrenewable energy resources, and they are depleting [2]. Among biofuels, biodiesel has emerged as an alternate renewable energy resource which is nontoxic and environment friendly [3]. Among biofuels, biodiesel has emerged as an alternate renewable energy resource which is nontoxic and environmentally friendly. Biofuels are obtained from natural resources. They contain a lesser amount of Sulphur, and as such lead to a very small release of oxides of Sulphur [4,5]. Based upon the feedstock/source and technology used for biofuel production, liquid biofuels can be categorized into three generations, namely first generation, second generation, and third generation biofuels [6]. First generation biofuels correspond to those which are produced from crops and edible oils. However, utilizing food crops as a source of biofuel presents some issues that limit the use of food crops in biofuel production. For instance, as it reduces the land available for agricultural purposes, this will lead to a shortage of food all over the world, in turn raising the prices of food. Deforestation may also arise in this situation, which may cause the destruction of habitats of wildlife and an ecological imbalance [7]. Second generation biofuels are produced from waste vegetable oils, non-edible plant seeds oil, and animal fats [8]. Second generation biofuel has certain advantages over the first-generation biofuels, e.g., non-edible oils are used for the production second generation biofuel which eliminates the competition for land used for food and feedstock because it is not used as a food material. Byproducts obtained are very useful because these can be utilized for heat and power generation [9]. Although second generation biofuels has solved the problems related to first generation biofuels, there are also certain limitations related to second generation biofuels, e.g., second generation biofuels have poor performance at lower temperatures. Furthermore, a large amount of saturated fatty acids is present in animal fats which make the process of transesterification difficult for biodiesel production. This difficulty has led to the search for third generation biofuel [10]. Algae can also serve as a source of bio fuel and algal oil based biodiesel is the third generation biofuel [11]. Microalgae are the organisms capable of photosynthesis and give the best yield of biodiesel [12]. Algae are the best source of biodiesel, because of their biodegradability, non-toxic nature, rapid growth, and such growth being independent of fresh water supply [1]. The algae are economically viable oil sources because they take less amount of water and energy while the oil productivity of algae is higher than other crops [13]. The transesterification of plant seeds or algal oils is the most widely adopted method to produce biodiesel at the micro as well as macro level. The transesterification process brings the viscosity of oil to a lower level. The transesterification process is collectively affected by the molar ratio, type of alcohol, temperature, reaction time, nature and amount of catalysts, reaction mode, and alcohol type. Enzymatic transesterification yields high purity biodiesel and glycerol. This process involves zero soap production and is also environment friendly. Lipases are frequently used for the transesterification of vegetable oils and fats from various sources [14]. Lipase enzyme has emerged as a most important industrial enzyme due to its vast applications. The lipase mediated transesterification process provides an easy approach to remove glycerol from the reaction mixture to bring equilibrium to the alkyl ester regime. Lipase assisted reactions are usually environment friendly and have limited space for side products. Lipase extracted from various sources and even microorganisms are immobilized on a suitable support for enhanced and prolonged usage [15]. Extracellular lipases are more accepted and need downstream extraction followed by immobilization on some feasible support for their repeated use. This approach develops sustainability in the transesterification process and helps to reduce the cost of the process. The current work was designed to optimize the process of lipase catalyzed transesterification of extracted Spirogyra oil as a feedstock and to study of the exhaust emission behavior.

Characterization of Spirogyra Oil
The physico-chemical properties including acid value, density, iodine value, viscosity, saponification value, and peroxide value of Spirogyra oil, as calculated by the American Oil Chemists Society (AOCS) methods, are given in Table 1. Acid value describes the presence of free fatty acids in oil. The observed acid value before acid transesterification of the algal oil (Spirogyra oil) under study was 16.67 ± 3.53 mg KOH/g. The observed value is comparable to 12.21 mgKOH/g of oil that was reported by Bhraatheraja et al. [16]. For base catalyzed biodiesel production, oil was subjected to acid esterification as a pre-step. After this step, the acid value was reduced from 16.17 ± 3.53 to 1.23 ± 0.53 mg KOH/g.
Iodine value describes the extent of unsaturation in oils [17]. The observed iodine value of the Spirogyra oil was 117.67 ± 13.01 mg I 2 /g. The saponification value is "the number of grams of NaOH required to completely saponify all the triglyceride esters in one gram of a particular oil" [18]. The saponification value of the spirogyra oil was found to be 165.33 ± 13.20 mg KOH/g, which was slightly lesser than the 173 mg KOH/g reported by Stanelay et al. [18].
"Density is a weight of unit volume of oil" [19]. The density of the Spirogyra oil under study was 0.86 ± 0.050 g/cm 3 , which is comparable to 0.883 g/cm 3 as reported by Phathak et al. [20].
The extent to which an oil sample undergoes primary oxidation can be defined by its peroxide value. The observed peroxide value of algal oil (Spirogyra) in our study was 4.63 ± 0.25 meq/kg that is comparable to 4.26 meq/kg revealed by Ojo-Awo, for the same algal oil [21]. According to International Olive Oil Council (IOOC) standards, a good oil should have less than 10 meq/kg peroxide value.

Summary Statistics of Selected Model
The biodiesel yield data acquired by chemical and enzymatic transesterification of Spirogyra oil was examined to select the appropriate statistical models. Selected response surface models were utilized for the optimization of different reaction conditions to get the maximum yield of biodiesel through chemical and enzymatic transesterification of algal oil. Based on the best fitted experimental data, (i.e., model significance, R 2 value, adjusted R 2 value, and lack of fitness test) quadratic models were selected out of linear, cubic, and 2F1 and quadratic models. The summary statistics of selected quadratic models for both chemical and enzymatic transesterification of the oil under study to biodiesel are presented below in Table 2. In model a, for the chemical transesterification of sample oil, p value, R 2 value, and adjusted R 2 value were <0.0001, 0.9933, and 0.987. However, in the case of model b for enzyme catalyzed biodiesel production, these values are <0.0001, 0.9954, and 0.9991, respectively. These summary statistics illustrate the validity of quadratic models for the chemical and enzymatic routes of biodiesel production.
Predicted vs actual graphs and normality plots for both models also helped to validate the quadratic model selection ( Figure 1). The linear distribution of data and absence of outliers in the normal plot of residues for both models predict the accuracy of the quadratic model. The predicted values of biodiesel yield were also in agreement with the actual/calculated values of biodiesel yield as illustrated by the normal distribution of data in predicted vs actual plots of both models.
Catalysts 2020, 10, x FOR PEER REVIEW 4 of 13 In model a, for the chemical transesterification of sample oil, p value, R 2 value, and adjusted R 2 value were <0.0001, 0.9933, and 0.987. However, in the case of model b for enzyme catalyzed biodiesel production, these values are <0.0001, 0.9954, and 0.9991, respectively. These summary statistics illustrate the validity of quadratic models for the chemical and enzymatic routes of biodiesel production.
Predicted vs actual graphs and normality plots for both models also helped to validate the quadratic model selection ( Figure 1). The linear distribution of data and absence of outliers in the normal plot of residues for both models predict the accuracy of the quadratic model. The predicted values of biodiesel yield were also in agreement with the actual/calculated values of biodiesel yield as illustrated by the normal distribution of data in predicted vs actual plots of both models.

Optimized Reaction Parameters and Optimum Yield
The optimum yield of biodiesel by the chemical transesterification of algal oil (Spirogyra) was achieved by carrying out the reaction for 90 min at reaction temperature of 45 °C using 1.13% catalyst (NaOCH3) concentration and a 6:1 methanol to oil molar ratio (Table 3). Renita et al. [22] also reported the optimization of different reaction parameters involved in algal oil-based biodiesel production using the response surface methodology. They revealed that the maximum yield of biodiesel was obtained when the reaction was performed at 60 °C using 0.3% by wt. catalyst (NaOH) and a 5:1 alcohol to oil molar ratio for 90 min [22].
In the case of enzymatic biodiesel production, the optimum yield was obtained by conducting the reaction for 42.5 h at the temperature of 35 °C using 1% enzyme (NOVOZYME-435) concentration and 4.5:1 methanol to oil molar ratio.

Optimized Reaction Parameters and Optimum Yield
The optimum yield of biodiesel by the chemical transesterification of algal oil (Spirogyra) was achieved by carrying out the reaction for 90 min at reaction temperature of 45 • C using 1.13% catalyst (NaOCH 3 ) concentration and a 6:1 methanol to oil molar ratio (Table 3). Renita et al. [22] also reported the optimization of different reaction parameters involved in algal oil-based biodiesel production using the response surface methodology. They revealed that the maximum yield of biodiesel was obtained when the reaction was performed at 60 • C using 0.3% by wt. catalyst (NaOH) and a 5:1 alcohol to oil molar ratio for 90 min [22]. In the case of enzymatic biodiesel production, the optimum yield was obtained by conducting the reaction for 42.5 h at the temperature of 35 • C using 1% enzyme (NOVOZYME-435) concentration and 4.5:1 methanol to oil molar ratio.

Analysis of Variance (ANOVA)
The impacts of various reaction parameters on the percentage biodiesel yield in the form of linear terms, first order interactions, and quadratic terms are described by the ANOVA in Table 4. The terms (a) and (b) represent the quadratic model for NaOCH 3 and NOVOZYME-435 catalyzed transesterification of Spirogyra oil, respectively. In Table 4, the terms having a p value < 0.05 were statistically significant. The linear terms A (catalyst concentration), B (methanol:oil ratio), and C (reaction temperature) were found to be significant for both models, while D (reaction time) was significant for model (a) only. For model (a), among the first order interaction terms, only AC (catalyst concentration × reaction time) was revealed to be significant with the p value 0.0008, while all other first order terms, i.e., AB, AD, BC, BD, and CD, were found to be insignificant with the p values greater than 0.05, i.e., 0.189, 0.728, 0.288, 0.467, and 0.938, respectively. On the other hand, for model (b), three first order interaction terms, i.e., AC, AD, and BC with p-values 0.005, 0.001, and 0.0145 were depicted to have significant effects on the model response (p-value < 0.05).
All the quadratic terms showed a significant influence on the NaOCH 3 catalyzed transesterification (Model (a)) with p values < 0.05. Meanwhile, in the case of enzyme catalyzed transesterification (Model (b)), the terms A 2 , B 2 , and C 2 have a significant quadratic effect with p values 0.0001, 0.019, and 0.0001, respectively. However, D 2 was insignificant with p value 0.3902.

Response Surface Plots for Chemical Transesterification
The 3D response surface plots are used to determine the process conditions that produce a desirable/maximum response (i.e., biodiesel yield resulted from the chemical transesterification of Spirogyra oil). The 3D plot for the only significant first order interaction term (A × C) is presented Catalysts 2020, 10, 1214 6 of 12 as Figure 2. The 3D plot shows that the optimum values for reaction temperature and catalyst concentration are 45 • C and 1.13%, respectively. The steep curves at the edges inferred that varying the reaction temperature or catalyst concentration above and below the optimum point can significantly reduce the biodiesel yield ( Figure 2). The 3D response surface plots are used to determine the process conditions that produce a desirable/maximum response (i.e., biodiesel yield resulted from the chemical transesterification of Spirogyra oil). The 3D plot for the only significant first order interaction term (A × C) is presented as Figure 2. The 3D plot shows that the optimum values for reaction temperature and catalyst concentration are 45 °C and 1.13%, respectively. The steep curves at the edges inferred that varying the reaction temperature or catalyst concentration above and below the optimum point can significantly reduce the biodiesel yield ( Figure 2).

Response Surface Plots for Enzymatic Transesterification of Algal Oil
The impact of interaction terms on the yield of biodiesel obtained by the NOVOZYME-435 catalyzed transesterification of algal oil is illustrated by 3D response surface plots (Figure 3). It can be observed from plots that the optimal response (biodiesel yield%) was achieved by using 1% enzyme concentration at 35 °C for 42.5 h with a 4.5:1 methanol to oil molar ratio. However, above and below these levels, a decline in the optimal response was observed.

Response Surface Plots for Enzymatic Transesterification of Algal Oil
The impact of interaction terms on the yield of biodiesel obtained by the NOVOZYME-435 catalyzed transesterification of algal oil is illustrated by 3D response surface plots (Figure 3). It can be observed from plots that the optimal response (biodiesel yield%) was achieved by using 1% enzyme concentration at 35 • C for 42.5 h with a 4.5:1 methanol to oil molar ratio. However, above and below these levels, a decline in the optimal response was observed.

Fuel Properties of Resultant Biodiesel
The fuel properties of synthesized biodiesel; which were calculated by the American Society for Testing and Materials (ASTM) standard methods, are given in Table 5. The kinematics viscosity of the Spirogyra oil-based biodiesel was depicted to be 5.87 ± 2.20 mm 2 /mL, which was slightly higher than 4.36 mm 2 /mL as reported by Ashokkumar et al. [23] and 5.52 mm 2 /mL reported by Ashokkumar et al. [23]. Biodiesel exhibits a higher kinematic viscosity than that of conventional diesel [23]. The kinematic viscosity of biodiesel increases due to high polarity in biodiesel as compared to petro-diesel

Fuel Properties of Resultant Biodiesel
The fuel properties of synthesized biodiesel; which were calculated by the American Society for Testing and Materials (ASTM) standard methods, are given in Table 5. The kinematics viscosity of the Spirogyra oil-based biodiesel was depicted to be 5.87 ± 2.20 mm 2 /mL, which was slightly higher than 5.52 mm 2 /mL reported by Ashokkumar et al. [23]. Biodiesel exhibits a higher kinematic viscosity than that of conventional diesel [23]. The kinematic viscosity of biodiesel increases due to high polarity in biodiesel as compared to petro-diesel [24]. According to international standard ASTM 6751, the value of kinematic viscosity ranges from 4 to 6 mm 2 /mL. Our reported value also lies in this range. The density of synthesized biodiesel was found to be 0.856 ± 0.03 g/cm 3 . The observed value was closer to 0.853 g/cm 3 that was described by Ashokkumar et al. [23]. In another previous study, the density for the algal oil is reported to be 0.866 g/cm 3 , which is also comparable with the value observed in current study. Biodiesel also possesses a higher density than conventional diesel, and that is why it produces a flame with less smoke. The density reported in this study is comparable with the value of 0.864 g/cm 3 according to ASTM D 6751 standard. The temperature at which the vapors over the fuel become flammable is known as flash point [25]. The observed value of flash point of Spirogyra oil-based biodiesel was 125.67 ± 2.11 • C, that was comparable to 140 • C as reported by Ashokkumar et al. [23], whereas it is slightly lower than 145 • C as revealed by Ahmad et al. [26]. The flash point is related to the safety of an engine. If the value of the flash point is higher than is considered safe to use, it becomes easier to store the biodiesel [24]. The flash point in our study falls within the range of 100-170 • C as described in ASTM D 6751. Pour point is the temperature at which the quantity of wax out of solution is adequate to gel the fuel [27]. In this study, the pour point of Spirogyra oil-based biodiesel was found to be −19.67 ± 0.8 • C, which was comparable to −19 • C as reported by Ashokkumar et al. [23]. However, the pour point value reported in another study was −10 • C, which is different than our observed value [28]. Fire point is the lowest fuel temperature at which the diffusion flame is sustained above the fuel pool without any external heat supply. The fire point of the sample oil-based biodiesel was depicted to be 138.66 ± 2.52 • C. According to international standards, fire point should range from 120 to 180 • C and our observed value falls in this range, owning to the good fuel properties biodiesel is getting attention as a renewable fuel [29]. The cloud point (CP) is referred to as the temperature at which crystals starts to form in the fuel [30]. In our study, the value of cloud point is observed to be −13.00 ± 1 • C. Cloud point affects the starting of a passenger car and heavy-duty engine. An engine shows good performance when the cloud point is around −20 • C. The above mentioned fuel properties have a large impact on the combustion of biodiesel and efficiency of the engine. Viscosity affects the starting of the engine. If the fuel is viscose, then there will be an incomplete combustion of fuel, as black smoke and incomplete combustion cause the lowering of engine power. Pour point and cloud point determine the lowest operating temperature, below these temperatures fuel become useless. Flash point is related to safety of fuel, and if the value of flash point is higher, then it is easy to use and easy to store at elevated temperatures.

Emission Profiling
To evaluate the impact of Spirogyra biodiesel blending on the emission characteristics of conventional diesel engine, NOx, CO, and HC were monitored upon combustion in an IC engine at full load ( Table 6). The comparison of pure biodiesel (S100) and neat diesel (D100) was also made on the basis of exhaust gas emissions. The findings reflected significant reductions in CO and HC for biodiesel blend (S5, S20, S40, and S100) when compared with conventional diesel. The reduction CO for S5 blend relative to D100 was 4.16% at full engine load. A reduction of 33.47% was calculated for S100 when compared with D100. The S20 blend exhibited a 16.36% reduction of CO emission as emitted by D100. Similar trends were observed for HC emissions and reductions in HC concentration were observed for all biodiesel blends in comparison with D100. The HC emissions were reduced by 7.48% for S5, 38.19% for S100, and 22.86% for S20 as compared with D100. However, NOx emissions were expectedly higher than D100. It was found that, by increasing the biodiesel fraction in blend, NOx emissions started to increase and the S100 blend exhibited 23.88% higher emissions than D100. The S5 blend showed a negligible rise of 2.55% in NOx when compared with D100, which can be tolerated. The high NOx values for Spirogyra biodiesel blends were probably due to the high oxygen contents of algal oil used for biodiesel synthesis [32]. The emission rate of CO and HC for biodiesel blends was substantially lower than the conventional diesel, which indicated the environment friendly domain of biodiesel from algal biomass.

Extraction of Spirogyra Oil
Algal samples were collected from the ponds situated in different areas of Gujart and were identified as Spirogyra crassa by one of the co-authors from the Institute of Industrial Biotechnology, GC University Lahore, Pakistan. Algal oil was extracted by Soxhlet apparatus using n-hexane and diethyl ether (1:1) as solvents. Extra solvent was removed on rotary evaporator under vacuum.

Physico-Chemical Characterization of Spirogyra crassa Oil
The oil extracted from Spirogyra crassa was characterized by measuring density, acid value (AV), saponification value (SV), peroxide value (PV), and iodine value (IV) using standard analytical protocols.

Experimental Design for Transesterification
Two central composite response surface designs consisting of 30 experimental runs were constructed separately for the chemical and enzymatic biodiesel production utilizing Design Expert 7. The reaction parameters selected for the optimization of the chemical transesterification of algal oil were arranged as catalyst concentration (0.25-2%), methanol:oil (3:1-9:1), reaction temperature (35-65 • C), and reaction time (40-150 min.), while for the enzyme catalyzed reaction, the reaction parameters were enzyme concentration (0.5-1.5%), methanol:oil (3:1-9:1), reaction temperature (15-55 • C), and reaction time (20-65 h). To perform the acid catalyzed esterification, 100 grams of oil was taken in a 250 mL three neck round bottom flask. Then, 0.05 g concentrated sulphuric acid (H 2 SO 4 ) and 2.25 g of methanol for each gram of free fatty acid (FFA) present in the oil were added to the flask. The reaction mixture was stirred for 120-180 min at 65 • C. The acid value was determined periodically after 15 min. Base catalyzed transesterification reactions were carried out in a 250 mL three necked flask. For this purpose, 50 g of oil was taken in a three neck flask. Then, the designated amount of catalyst NaOCH 3 was added in alcohol according to the central composite rotatable design (CCRD) and this was transferred into the flask containing Spirogyra oil (algal oil) that was attached to a thermometer, condenser, and magnetic stirrer. The reaction mixture was stirred according to the CCRD design at a specific temperature for a designated time. Spirogyra oil and methanol were mixed together and then NOVOZYME-435 was added to this mixture. After that, the reaction mixture was placed in a shaker incubator. The reaction conditions were selected as per CCRD. At the end of reaction, enzyme was separated from the reaction mixture through filtration process. Biodiesel was separated from glycerol and was purified.

Statistical Optimization
Analysis of variance (ANOVA), diagnostic checks, 3D response surface plots, and descriptive statistics were built to study optimization process. Based upon experimental results, the best fitted model was selected by considering the following parameters: lack of fit values, statistical significance of selected model, and higher values of R 2 and adjusted R 2 .

Biodiesel Characterization
Chemical characterization of the synthesized biodiesel was performed by FTIR spectroscopy (Carry-660-Agilent Technologies, Santa Clara, CA, USA) and GC-FID (Shimadzu, Tokyo, Japan) techniques. FTIR analysis was performed to confirm the conversion of fatty acid into fatty acid methyl esters using an FTIR spectrophotometer. Spectra were taken for a scanning range of 400-4000 cm −1 . Major fatty acid methyl esters (FAME) were detected by gas chromatography equipped with a flame ionization detector (FID). The capillary column used was made of fused silica (with 30 m × 0.25 mm with 0.25 µm film thickness). The controlled column temperature program was used and the initial temperature was maintained at 100 • C for 4 min. Then, it was increased to 220 • C at the rate of 3 • C per minute and maintained for 4 min, followed by an increase in temperature up to 260 • C with a hold-up time of 10 min. Temperatures of the injector and detector were set at 250 • C and 260 • C, respectively. With a flow rate of 1.0 ml/min, Helium was used as a carrier gas. Varian WS software was used to record the chromatogram. Fatty acids were identified by a comparison of the relative retention times of FAME peaks from samples with those of reference standards procured from Sigma-Aldrich (St. Louis, MO, USA).

Fuel Properties of Produced Biodiesel
The fuel properties of Spirogyra oil-based biodiesel were estimated by performing standard ASTM tests for the following properties: density (ASTM D 5002), Fire point, flash point (ASTM D93), kinematic viscosity (ASTM D445), cloud point (ASTM D2500), and pour point (ASTM D97).

Exhaust Emission Profiling
Biodiesel synthesized from Spirogyra oil was mixed with fossil diesel to evaluate the emission profile of blends at full engine load conditions. The B100 (Diesel 100%), S5 (Spirogyra biodiesel 5% and diesel 95%), S20 (Spirogyra biodiesel 20% and diesel 80%), S40 (Spirogyra biodiesel 40% and diesel 60%), and S100 (Spirogyra biodiesel 100%) blends were prepared and combusted at 100% load. The internal combustion engine (IC) used to quantify exhaust gas emissions was a diesel engine having 11.75 KW power with bore stroke 110 × 125 mm at 2200 rpm. The minimum fuel consumption was 2.5 L/hr. The engine was operated at 100% load to measure gaseous emissions. Testo 350 portable emission analyzer was employed to measure CO, NOx, and HC emissions upon burning the fuel fractions.

Statistical Analysis
Statistical analysis of all the experimental results was performed using SPPS statistical software (Chicago, IL, USA) and Design Expert-7, Stat Ease (Minneapolis, MN, USA).

Conclusions
A locally isolated Spirogyra crassa was found to be a good source of oil which was used for the synthesis of biodiesel. Based on the acid value, saponification value, peroxide value, density, viscosity, and iodine values, spirogyra oil was found to be suitable for biodiesel production. Fuel properties, such as flash point, fire point, cloud point, density, and kinematic viscosity of the spirogyra-based biodiesel were found to be within the limits of ASTM standards. The biodiesel production process was monitored by FTIR spectroscopy and the fatty acid profiling of resultant biodiesel was done by GC-FID analysis. Based on biodiesel characterization, it was ascertained that the synthesized biodiesel exhibited technically compatible fuel characteristics and hence may be used as a potential green fuel.