1 Introduction

Diesel engines are used in transportation, power plants, construction, and rural agricultural and industrial activities; consequently, it has led to increasing in demand for petroleum-based diesel (Boggavarapu and Ravikrishna 2013), while fossil fuel reserves in the world are limited. Also, the problems of air pollution and global warming have been becoming even more critical than ever. Scientists worldwide have been working diligently to find out renewable, carbon–neutral, and environmentally friendly fuels to replace the petroleum-based diesel. As shown in previous reports (Rajasekar et al. 2010; Altin et al. 2001; Fukuda et al. 2001; Sayin and Canakci 2009; Han et al. 2010; Kannan et al. 2011; Macor et al. 2011), biodiesel fuel, oxygenated, biodegradable, non-toxic, and environmentally friendly fuel, has been considered as a very promising alternative fuel to replace traditional diesel fuel.

Biodiesel produced from various resources such as rapeseed, soybean, cottonseed oil, palm oil, jojoba oil, sunflower has been used in internal combustion engines without major modifications as reported by Muralidharan and Vasudevan (2011). Saravanan et al. (2010) also investigated the combustion characteristics of a heavy commercial vehicle compression-ignition engine fueled with crude rice bran oil methyl ester (CRBME). Consequently, when comparing CRBME with diesel fuel they found that the delay period was shorter by about 15%, the peak pressure was slightly lower, the maximum heat release rate and the thermal brake efficiency were 34% and 8% lower, respectively; meanwhile, the brake specific energy consumption (BSEC) was about 18% higher. Qi et al. (2009) tested biodiesel produced from crude soybean oil on a single-cylinder, naturally aspirated, and direct injection diesel engine. They observed that the peak cylinder pressure of biodiesel was higher at lower engine loads and identical at higher engine loads, and combustion started earlier at all engine loads. They also showed that the power output of the biodiesel engine was almost the same as that of a diesel engine under-speed characteristic at full load. Under almost all engine speed ranges, the BSEC of biodiesel was closer than that of diesel. In another research, Huang et al. (2010) investigated two different biodiesels produced from pistachio and jatropha to compare performance and emission characteristics when they were used for a diesel engine. They found that exhaust emissions could be reduced by using biodiesel. Indeed, carbon monoxide (CO) and hydrocarbon (HC) emissions were reduced at high engine loads. Moreover, nitrogen oxides (NOx) and smoke emissions were also reduced dramatically at different engine loads. Also, the engine performance and emissions run by pistache were very similar to those run by jatropha biodiesel.

Compared to petroleum-based diesel, the high cost and most of the biodiesels produced from edible oils such as rapeseed oil, sunflower oil, and palm oil are major barriers to commercialize. Approximately 70%–80% of the total biodiesel production cost from the raw material cost (Meng e al. 2008). Moreover, the use of these oils would cause the competition of farming land for food and fuel supply, which results in oil and food price inflation (Huang et al. 2010). Therefore, the use of low-cost, non-edible feedstock such as waste cooking oil is expected to be competitive in price with petroleum diesel and to ensure food security in the world. Furthermore, the use of waste cooking oil as an engine fuel also contributes to reducing environmental problems due to the waste-oil disposal process.

In their experiment with waste palm oil (WPOME) and canola oil methyl esters (COME), Necati et al. (2009) observed that the maximum engine torque slightly dropped. At the same time, the BSFC increased in comparison with those of the petroleum-based diesel fuel (PBDF). The maximum brake torques for PBDF, WPOME, and COME at 1500 rpm corresponding to the full load condition were 328.69, 320.24, and 319.80 N m, respectively. The BSFC of WPOME and COME increased by 7.48% and 6.18%, while thermal brake efficiency reduced by 1.42% and 0.12%, respectively. In another research, Muralidharan and Vasudevan (2011) investigated the effects of compression ratio on characteristics of a variable compression ratio engine using methyl esters of waste cooking oil and diesel blends. As a result, the thermal brake efficiency for B40 significantly improved at a compression ratio of 21 in comparison to that of standard diesel. The specific fuel consumption of the blend B40 at the compression ratio of 21 was 0.259 kg/kWh, whereas it was 0.314 kg/kWh in the case of standard diesel.

Although there have been many investigations, as listed above, in the useability of waste cooking oil on compression-ignition engines, these investigations used biodiesels produced from waste cooking oil throughout the transesterification reaction directly waste cooking oil to fuel for the engine. Also, these studies only focused on testing at some operating engine points, such as speed characteristics at full load or load characteristic at rated engine speed. For these reasons, the objectives of this study are to produce biodiesel from waste cooking oil and investigate the compression-ignition engine performance and its combustion characteristics fueled by waste cooking oil synthetic diesel (WCOSD) corresponding to all main operating engine points.

2 Catalytic cracking process of waste cooking oil

Waste Cooking Oil (WCO) was collected from local restaurants in Hanoi city in Vietnam. Catalytic cracking manipulations were carried out at 450 °C in a rounded bottom one-liter batch reactor in the presence of 5 wt% MgO catalyst, as showed in Fig. 1. For each experiment, 500 g of sample and 25 g of MgO were placed in the reactor. The reactor temperature was gradually raised to 450 °C by an electric furnace at heating rates of 10 °C/min and kept at isothermal condition until no more vapour. We use an AC electrical source (220 V and 4 A) to supply for the electric furnace. It took 40 min to reach an operating temperature of 450 °C, and then this temperature is continuously controlled by turn ON and OFF the electrical source. We got the first litre of biodiesel after 40 min, and then it took 40 min to get one more litre of the biodiesel. The average electrical cost to produce 1 L of biodiesel is approximately a quarter of the price of diesel on the market. Also, by using waste cooking oil as raw material, it will reduce the cost of paying for disposing of waste cooking oil. The vapour was allowed to pass through a condenser to collect WCOSD in the liquid phase.

Fig. 1
figure 1

Principle diagram of the WCO cracking system

In our production process, the catalyst only was added to the reactor after the temperature of the reactor reached the operating temperature of 450 °C. The valve connecting the reactor and condenser is opened 20 min after the catalyst added to the reactor. Therefore, the temperature for catalytic cracking always controlled at approximately 450 °C. The cracked products compose of naphtha (approximately 2.9%), kerosene (approximately 8.7%), diesel (67% including), and residue (21.4%). It needed approximately 1.5 L of waste cooking oil to produce 1 L of biodiesel. We repeated the production process five times, and observed that the yield and composition of the cracking product were quite stable as the raw materials were the same. One disadvantage of using fixed-bed of catalysts is that it might be necessary to change the catalysts quite often as byproducts can contaminate on the surface of the fixed-bed, hence reducing the contact area between the vapours and the catalysts and affecting the quality of the biodiesel. In addition, it might be more challenging to change catalyst fixed in the heated bed, and the product prices might be increased due cost for preparing catalyst beds. The catalyst was mixed to the raw materials in the reactor so that the effect of a catalyst on the cracking reactions was maintained stable. Moreover, changing the catalyst was pure as the catalyst was taken out together with byproducts. In our experiment, we have prepared 20 L of biodiesel for all tests, performance test, and fuel property tests. Although the volume of the reactor is approximately 1 L, our production process is continuous. When the biodiesel was taken out from the condenser, the raw materials and catalyst were added to the reactor at the same time.

The fuel properties of WCOSD products were evaluated to compare to regular diesel fuel using ASTM methods. Cetane number, density, kinematic viscosity, flash point, carbon residue, ash, sulfur and the calorific value of WCOSD were characterized. Cetane number was determined by comparing its combustion characteristics in a test engine with those for blends of reference fuels of known cetane number under standard operating conditions (ASTM D-613). A digital density analyzer was used to measure the sample at 25 °C temperature (ASTM D-4052). Kinematic viscosity was determined using a U-tube viscometer (ASTM D-445). Flashpoint of WCOSD was determined by filling the test cup with WCOSD to the filling mark inside of the test cup, and the lighted test flame was passed along the circumference of the cup (ASTM D-92). The calorific values of the samples were determined using a bomb calorimeter (ASTM D-240). Carbon residue was calculated through the amount of carbon residue left after evaporation and pyrolysis of the sample (ASTM D-189). Ash was calculated by igniting and burning samples until only ash and carbon remain (ASTM D-482). The sulfur content was determined using an energy-dispersive X-ray fluorescence analyzer (ASTM D-4294).

3 Testing equipment, experiment setup, and test procedure

3.1 Test fuels and engine used in the experiment

In this study, the waste cooking oil synthetic diesel successfully produced from waste cooking oil in this research was used and compared with conventional diesel fuel when they were used to run on an internal combustion engine. The physical and chemical properties of WCOSD and CD fuels are shown in Table 1. The test engine is a four-stroke, single-cylinder, water-cooled, naturally aspirated, direct injection diesel engine.

Table 1 Physical and chemical properties of tested fuels

3.2 Test setup and experimental procedure

Figure 2 shows the schematic diagram of engine testbed, including a test engine, chassis dynamometer, exhaust gas analyzer device, control unit, fuel consumption device, airflow measurement instrument, and temperature sensors. To conduct the specific engine speed, the experiments were conducted with the single-cylinder diesel engine corresponding to various engine speeds. In the experiment, the engine was coupled with a 40 kW regenerative dynamometer. The cylinder pressures were recorded by a high-speed data acquisition system, including two high accuracies of piezoelectric pressure transducers, a crank angle encoder, and a combustion analyzer device. The fuel consumption device determined the fuel rate supplied for the test engine. In order to measure the airflow rate, the air consumption meter was set up on the intake manifold of the test engine. Also, six different digital thermocouples were set up to measure the exhaust gas, engine oil, coolant inlet and outlet, fuel, and air inlet temperature. Furthermore, the ambient temperature, air density, and relative humidity also were recorded. To control the engine and dynamometer, the control system was used to; consequently, it collected signals from measuring equipment and displayed measuring results. The exhaust emissions of the tests, including CO, CO2, Hydrocarbon (HC), O2 and NOx were measured by an exhaust gas analyzer device manufactured for measuring internal combustion engine emissions. The characteristics of the measuring instruments and the gas analyzers are presented in Table 2.

Fig. 2
figure 2

Schematic diagram of the engine testbed and completed engine testbed in the experiment

Table 2 Accuracies of the measuring instruments and the gas analyzers

4 Results and discussions

4.1 Comparison of properties between WCOSD and diesel fuels

The properties of WCOSD are showed in Table 3 and compared to the standard Euro V specification of diesel fuel. The cetane number of WCOSD was slightly lower than diesel fuel due to the content of unsaturated components; that could inhibit the combustion of the fuel in the engine. Another disadvantage was the low calorific value of WCOSD because of the high content of oxygenates compounds (Wako et al. 2018), which had a worse effect on the performance of the engine. The viscosity of the biodiesel was slightly higher than that of diesel fuel, which caused worse atomization in the engine and probably reduced the combustion efficiency due to the formation of carbon deposits contaminating in the combustion chamber. However, WCOSD had some advantages such as completely free of sulfur, free of ash content, and carbon residue as compared to diesel fuel. The properties of WCOSD were found to be closer to regular diesel fuel; hence regular diesel was used as a comparison fuel in the engine performance test.

Table 3 Fuel properties of WCOSD compared to EN 590:2009 standard specifications of diesel fuel

4.2 Comparison of engine performance characteristics

Figure 3a shows a comparison of the engine performance at different engine speeds and full load conditions when WCOSD and CD were utilized as test fuels. Generally, the engine performance was entirely consistent over the engine speed range from 1400 to 2100 rpm. Indeed, when CD used as a fuel, the brake powers at engine operating speeds of 1400 rpm and 1700 rpm were, respectively, 2.90%, 2.43% higher in comparison with those of WCOSD. Also, the fuel consumption characteristics of the test engine in case of using WCOSD were higher than those in the case of using CD, as shown in Fig. 3b, which probably resulted from WCOSD lower calorific value, as shown in Table 1. Moreover, the density and kinematic viscosity of diesel were higher than those of WCOSD, which also contributed to a reduction of the engine power because of an increase in the friction loss. However, as shown in Fig. 3a at high speed, the engine power in the case of using WCOSD was slightly higher than that of CD, which resulted from the effect of viscosity. Since the WCOSD viscosity was smaller than the CD viscosity, the mixture of WCOSD and air became more advantageous compared to that of CD, especially in case of high engine speeds as the duration for mixture formation was limited.

Fig. 3
figure 3

Comparison of engine characteristics a engine power and b fuel consumption

Figure 4 presents the variation of brake specific fuel consumption (BSFC) corresponding to each constant engine speed of 1400, 1700 and 2100 rpm and the engine torque ranging from 0 to 50 N m when the test engine fueled with WCOSD and CD. The results showed that the BSFC of WCOSD was always higher than that of CD at every engine operation point. At the same operating conditions, the highest difference in BSFC between the two fuels is 19% at the operating point of 1700 rpm engine speed and 25% load. Meanwhile, the BSFC of the two fuels was similar at 75% of the maximum torque. This trend is the same as those concluded from Meng et al. (2008), Necati et al. (2009), Hirkude and Padalkar (2012), Zhu et al. (2011), Di et al. (2009) and Necati and Canakci (2010) investigating two types of biodiesel derived from waste palm oil and canola oil. In order to maintain the same power output, a higher amount of WCOSD should be supplied, as suggested by Muralidharan and Vasudevan (2011), Buyukkaya (2010), Hirkude and Padalkar (2012), Zhu et al. (2011) and Di et al. (2009) due to the lower calorific value of WCOSD compared to CD.

Fig. 4
figure 4

Brake specific consumption of the test engine fueled CD and WOCSD at a 1400 rpm, b 1700 rpm, c 2100 rpm, and d full load

The lower output power and higher fuel consumption of WCOSD led to the lower brake thermal efficiency (BTE) in comparison to that of CD at all engine operating conditions, as depicted in Fig. 5. For example, at the same operating condition of 1400 rpm and 70% of load condition, the BTE of the engine fueled with CD reached the highest value of 38.3% while that fueled with WCOSD was 36.6%. Notably, at the operating point of 1400 rpm and 25% of load, the difference in BTE between WCOSD and CD was as high as approximately 21%. The second reason for these results can be explained by the higher viscosity and weak volatility of WCOSD, resulting in more poor atomization and combustion characteristics, as described in results concluded in Hirkude and Padalkar (2012) and Necati and Canakci (2010).

Fig. 5
figure 5

Brake thermal efficiency of the test engine fueled CD and WOCSD at a 1400 rpm, b 1700 rpm, c 2100 rpm and d full load

4.3 Comparison of combustion characteristics

Combustion characteristics of WCOSD and CD in this research were investigated based on means of in-cylinder pressure and ignition delay. To analyze the combustion process, the in-cylinder pressure and fuel line pressure data of 200 cycles with a 0.4° resolution of crank angle were measured and analyzed. Figure 6a shows the variation of in-cylinder pressure versus crank angle when the test engine fueled with CD and WCOSD fuels at a speed of 1400 and various engine loads of 11, 23, and 35 N m. The observed in-cylinder pressure peaks for the engine running with WCOSD were lower than those of CD by 0.43, 0.32, and 0.74 bar at 11, 23, and 35 N m, respectively. However, the in-cylinder pressures were quite similar in the areas far from the top dead center. The lower in in-cylinder pressure peaks can result from the improper mixing of WCOSD with air at low engine temperature due to its characteristics.

Fig. 6
figure 6

Variation of in-cylinder pressure of the test engine fueled CD and WOCSD at a 1400 rpm, b 1700 rpm, c 2100 rpm, and d ignition delay at different operating conditions

Figure 6d compares the ignition delay, which is defined as the time interval between the start of injection and the start of combustion, of the test engine fueled by WCOSD and CD at different operating conditions. It can be observed that the ignition of the WCOSD started earlier than that of CD by from 0.4 to 0.8°CA. The advanced ignition start of WCOSD results from the physical properties of WCOSD (Tesfa et al. 2013). Also, the ignition delay for WCOSD was shorter than that for CD at low and medium load, whereas the opposite result was found at high loads, as shown in Fig. 6d.

4.4 The compassion of exhaust emissions

4.4.1 Comparison of carbon monoxide emissions

Figure 7 shows the experimental results of carbon monoxide (CO) emissions from the test engine fueled WCOSD and CD. It can be seen that the trends of CO emissions from the engine fueled with the two fuels were similar to each other. The CO emissions were low at the low and medium loads and high at the full loads. The main reason for this phenomenon is that the mixtures at full load were more abundant than those at low and medium loads, resulting in a lack of oxygen in the combustion process at full load conditions. At full load conditions, the CO emissions of the engine fueled with CD were higher than that with WCOSD, 34.85% higher at 1400 rpm, and 58.33% higher at 1700 rpm. However, the trend was opposite at high engine speed. At 2100 rpm, when the test engine fueled with CD, the CO emissions were 45.9% lower than that fueled with WCOSD.

Fig. 7
figure 7

Carbon monoxide emissions of the test engine fueled CD and WOCSD at a 1400 rpm, 1700 rpm, 2100 rpm and b full load

4.4.2 Comparison of nitrogen oxides emissions

Figure 8 shows the variation of nitrogen oxides (NOx) emissions versus engine speeds and loads. At the same operating conditions, the NOx emissions produced by WCOSD were higher in comparison to that of CD. The highest NOx emissions produced by WCOSD were 1165, 1140, and 846 at 1400, 1700, and 2100 rpm, respectively, whereas those of CD were respectively 1150, 1023, and 833 ppm. The higher NOx emission of the test engine in case of using WCOSD might result from the provision of the oxygen content in WCOSD, which probably contributed to the formation of NOx. Another factor that caused the increase of NOx emission is the higher peak temperature during combustion for WCOSD compared to diesel.

Fig. 8
figure 8

NOx emissions of the test engine fueled CD and WOCSD at a 1400 rpm, 1700 rpm, 2100 rpm and b full load

4.4.3 Comparison of hydrocarbon emissions

The hydrocarbon (HC) emissions of the test engine running on both WCOSD and CD were found to be very low at all engine operating conditions. The variations of HC emissions between two types of fuels at the 12 operating conditions tested in this study is shown in Fig. 9. It can be seen that under most operating conditions, the HC emissions of test engines running on WCOSD were lower than those of CD. The HC emission of the engine fueled by WCOSD reduced by 26.3% on average compared to that of the engine fueled by CD. From these results, we can conclude that the use of WCOSD generally resulted in lower HC emissions due to its clearer combustion. Besides, at full load conditions, when the engine speed increased from 1400 to 2100 rpm, the HC emission of an engine running on two types of fuel significantly reduced due to the higher temperatures leading to better atomization and volatility.

Fig. 9
figure 9

Hydrocarbon emissions of the test engine fueled CD and WOCSD at a 1400 rpm, 1700 rpm, 2100 rpm and b full load

4.4.4 Comparison of smoke emissions

Figure 10 presents the smoke emission experimental results of the test engine fueled WCOSD and CD. The trends of black smoke emissions from the engine fueled with both two tested fuels were similar. The smoke emissions were low at the low and medium loads and high at the full loads. The main reason for this phenomenon is that the mixtures at full load were substantially richer than these at low and medium loads, leading to the oxygen lack in the combustion process when the engine operated at full load conditions. Also, it can also be found that the average amount of black smoke emissions as the engine fueled with WCOSD was 17% lower than that with CD. At full load conditions, with both fuels, the smoke emissions from the engine increased the speed accordingly, as seen in Fig. 10b. This phenomenon can be explained that when the engine speed increased, the timings for fuel evaporation and mixing processes became shorter, which reduced the combustion quality.

Fig. 10
figure 10

Smoke emissions of the test engine fueled CD and WOCSD at a 1400 rpm, 1700 rpm, 2100 rpm and b full load

5 Conclusions

In this paper, waste cooking oil synthetic diesel from waste cooking oil was produced by catalytic cracking in a batch reactor using MgO as a catalyst and used as investigated fuel. The engine fueled with WCOSD and CD to compare the engine characteristics, including engine power, fuel consumption, combustion process, and emissions. The results showed that the produced biodiesel is suitable in quality for running on diesel engines. Although the engine brake power of WCOSD slightly dropped at low and medium engine speed due to the lower of its heat value, it slightly increased at high engine speed since the ower viscosity of WCOSD enhanced air–fuel mixture formation in the combustion chamber. Furthermore, the BSFC of the test engine running on WCOSD increased at almost all engine operating conditions. In contrast, the in-cylinder pressure peaks in the engine running with WCOSD were lower than those of CD by 0.43, 0.32, and 0.74 bar at 11, 23, and 35 N m, respectively. Besides, the emissions of nitrogen oxides of the test engine fueled WCOSD were higher than those of CD at all tested conditions. The hydrocarbon was lower for WCOSD in comparison to those of CD at almost all operating conditions. The HC emission of an engine fueled by WCOSD averagely reduced by 26.3%. The smoke emission of the test engine in case of using WCOSD was 17% lower on average than that of CD. However, the carbon monoxide emissions were lower at the low and medium loads and higher at the full loads. For future research, we will focus to scale our system for commercial production as well as apply WCOSD for worldwide diesel vehicles.