An Experimental Analysis of Soybean Straw Combustion on Both CO and NOX Emission Characteristics in a Tubular Furnace

In this study, an experiment is conducted to explore the potential to protect both the environment and resource shortage of soybean straw, for combustion in a tubular furnace. Then, the combustion characteristics, gas emissions, and energy consumption of soybean straw are analyzed at a combustion temperature range of 773–1173 K. The results show that the total emissions of CO and NOX are the largest at a temperature of 873 K. For NOX, the emission time is significantly improved at temperatures of 973–1173 K. At high temperatures, the reaction of NOX with CO and coke reduces the total emission of NOX. The average weight loss rate at combustion temperatures of 973, 1073, and 1173 K increased by 27.38%, 61.47% and 77.97%, respectively, relative to that of 873 K. However, the energy consumption increases with the increase in combustion temperature, resulting in unnecessary waste. To get an optimal characteristic between energy utilization and pollutant discharge, a temperature range of 873–973 K is determined as the appropriate temperature for burning soybean straw.


Introduction
Energy conservation and environmental improvement, common concerns of humankind, are very important to social development all the time [1], especially for energy consumption [2], energy conversion [3] and energy saving [4]. According to the statistics of the proven energy reserves in the world, oil could still be mined for 40.5 years, natural gas for 66.7 years, and coal for 164 years [1]. With the increase in the demand for energy, it is difficult to meet the demand for a single energy supply mode of fossil fuel [1,5]. Meanwhile, the environmental problems caused by fuel combustion need to be considered [6]. The establishment of a diversified energy supply system can alleviate energy shortage and environmental pollution. Therefore, many scholars turn to the development, utilization and transformation technology of renewable energy [7].
Biomass is popular around the world because of its wide distribution, great energy storage [8,9], and its renewable and environment-friendly characteristics [10][11][12]. Biomass is considered to be a potential renewable resource [8] and it is widely used in thermal energy production, power generation, and liquefaction and gasification to produce biofuels [13]. Over 400 million tons of biomass waste is generated in China each year [14]. Soybean is one of the most widely grown cereal crops, however, throw away or burn in the field is regarded as the common management of soybean straw [15]. For soybean straw occupying a lot of land resources, and generating many pollutants during combustion, this article explores the appropriate soybean straw combustion temperature to avoid wasting resources and polluting the atmosphere.

Sample Preparation
The soybean straw used in the experiment was from Meizhou City, Guangdong Province, China. It was dried at 378 K for 24 h in a desiccator (Yike Instrument and Equipment Co., Ltd. 101 A. Chengdu, China); the material was ground and screened into powder with a particle size of 80 meshes. The powder was packed into a sealing bag and saved in a drying basin on standby. Elementary analysis (based on the dry basis) and proximate analysis (based on the wet basis) were based on the ASTM D5373 standard and the E0870-82R98E01 standard, respectively; results are shown in Table 1.

Apparatus and Methods
As shown in Figure 1, the combustion characteristics of soybean straw at different temperatures were investigated in a tubular furnace (Yahua Furnace CO., LTD. SK2-4-13, Wuhan, China). The inner combustion chamber of the furnace was a quartz tube, and the temperature was detected by a thermocouple. The experimental combustion temperature was set to 773, 873, 973, 1073 and 1173 K, adjusted by an intelligent temperature controller with a deviation value of 1.5 K. Air at a flow rate of 0.1 m 3 /h was passed for 15 min before the start of the experiment to stabilize the gas flow in the reaction chamber. Each time 0.1 g soybean straw powder was placed in a porcelain boat (45 mm in length), measured by electronic balance with a resolution of 0.1 mg, and sent into the high-temperature zone by an iron hook. The flue gas generated by the reaction was analyzed by a flue gas analyzer Energies 2020, 13, 1587 3 of 12 (Leshi Alliance Technology CO., LTD, ECOM-J2KNIB, Beijing, China), the data acquisition time was 1 s, and the result was recorded by a computer. The remaining part of the flue gas was collected by a gas bag for further investigation and the rest was discharged, after treatment to a harmless state by the effluent gas treatment system. The solid residues in the porcelain boat were weighed with an electronic balance.
Energies 2020, 13, x FOR PEER REVIEW 3 of 12 temperature zone by an iron hook. The flue gas generated by the reaction was analyzed by a flue gas analyzer (Leshi Alliance Technology CO., LTD, ECOM-J2KNIB, Beijing, China), the data acquisition time was 1 s, and the result was recorded by a computer. The remaining part of the flue gas was collected by a gas bag for further investigation and the rest was discharged, after treatment to a harmless state by the effluent gas treatment system. The solid residues in the porcelain boat were weighed with an electronic balance.
where is the volume of the tubular furnace, m 3 ; is the sectional area of the tube, m 2 ; is the length of the tube, m; is the diameter of the tube, m; and is the air volume flow, m 3 /h. The value of is 1.5 m, is 0.07 m and is 0.1 m 3 /h as the tube furnace specifications and experimental project setup; then the value can be obtained as 9.69 s.

Volume Reduction Rate
where is the yield of solid residue, is the weight of the material, g; is the weight of solid residue, g; and is the volume reduction rate.

Energy Consumption and Proportion
where V t is the volume of the tubular furnace, m 3 ; S is the sectional area of the tube, m 2 ; L is the length of the tube, m; D is the diameter of the tube, m; and q v is the air volume flow, m 3 /h. The value of L is 1.5 m, D is 0.07 m and q v is 0.1 m 3 /h as the tube furnace specifications and experimental project setup; then the value t s can be obtained as 9.69 s.

Volume Reduction Rate
where η s is the yield of solid residue, m o is the weight of the material, g; m s is the weight of solid residue, g; and η v is the volume reduction rate.

Energy Consumption and Proportion
W r = P n t r , Energies 2020, 13, 1587 4 of 12 W n = P n t n , where S 1 is the heating section area of the tubular furnace, cm 2 ; L 1 is the length of the heating section, it is 77 cm as the tube furnace specification; P n is the electrical power, kW; and P e is the electrical power per unit area, kW/cm 2 . When the temperature is 773, 873, 973, 1073 and 1173 K, the electrical power per unit area is 0.0006, 0.0008, 0.001, 0.0013 and 0.0016 kW/cm 2 , respectively [10]; W r , is the power consumption cost by temperature-rise period, kWh; t r is the heating-up time, h; W n is the electric energy consumption, kWh; t n is the experiment time, h; and η is the cost proportion of W r . Figure 2 shows the CO emission concentration regularity under different temperatures. The peak concentration of CO rises first and then decreases, indicating that CO has undergone a strong formation reaction, which is closely related to temperature. The maximum peak concentration of CO was 3215 ppmv, which was 200 times as large as the minimum (16 ppmv).

CO Emission
Energies 2020, 13, x FOR PEER REVIEW 4 of 12 where 1 is the heating section area of the tubular furnace, cm 2 ; 1 is the length of the heating section, it is 77 cm as the tube furnace specification; is the electrical power, kW; and is the electrical power per unit area, kW/cm 2 . When the temperature is 773, 873, 973, 1073 and 1173 K, the electrical power per unit area is 0.0006, 0.0008, 0.001, 0.0013 and 0.0016 kW/cm 2 , respectively [10]; , is the power consumption cost by temperature-rise period, kWh; is the heating-up time, h; is the electric energy consumption, kWh; is the experiment time, h; and is the cost proportion of . Figure 2 shows the CO emission concentration regularity under different temperatures. The peak concentration of CO rises first and then decreases, indicating that CO has undergone a strong formation reaction, which is closely related to temperature. The maximum peak concentration of CO was 3215 ppmv, which was 200 times as large as the minimum (16 ppmv). The total CO emissions at different temperatures are shown in Figure 3. The slope of the curve shows that the CO overflow rate increased at first, then decreased, with a maximum value of 127.5 ppmv/s at 873 K. However, the total emission also first increased and then decreased just like the variation tendency found in the literature [20,23]. Total emission arrived at 873 K, with its peak value as 354,570 ppmv, which was 194.61 times as large as the minimum (1822 ppmv). This may be because 873 K is an excess temperature from incomplete combustion to complete combustion, whereas, CO can hardly overflow at 1173 K, indicating that soybean straw burned to a complete state. The total CO emissions at different temperatures are shown in Figure 3. The slope of the curve shows that the CO overflow rate increased at first, then decreased, with a maximum value of 127.5 ppmv/s at 873 K. However, the total emission also first increased and then decreased just like the variation tendency found in the literature [20,23]. Total emission arrived at 873 K, with its peak value as 354,570 ppmv, which was 194.61 times as large as the minimum (1822 ppmv). This may be because 873 K is an excess temperature from incomplete combustion to complete combustion, whereas, CO can hardly overflow at 1173 K, indicating that soybean straw burned to a complete state.

CO Emission
The effects of temperature on the important parameters of CO emission are shown in Table 2. In order to obtain an exact value, the residence time of CO in the tubular furnace (t s = 9.69 s) should be subtracted. The time CO stays in the filter bank and the time for signal conversion and transmission should be ignored due to their small values.  The effects of temperature on the important parameters of CO emission are shown in Table 2. In order to obtain an exact value, the residence time of CO in the tubular furnace ( = 9.69 s) should be subtracted. The time CO stays in the filter bank and the time for signal conversion and transmission should be ignored due to their small values. As seen from Table 2, the output time of CO is brought forward with a rise of temperature, and the maximum extent is about 7 s. It is made clear that volatile overflowed more easily. It should be on this account that the output of volatile is in close relation to heat flux [24]. From the point of view of heat transport, with higher combustion temperature, the material has a larger thermal gradient and heat flux from inside to outside, and its temperature rose more rapidly to improve the material drying degree and volatile precipitation. From the point of view of mass transfer, under lowtemperature levels, pyrolysis plays a major role in the initial stage of combustion, whereas a large amount of coke formed by incomplete pyrolysis in the outer layer of material, which will have reactions with the overflow of volatile and even block the volatile [25]. In addition, the CO reached its maximum emission level at 221 s. As the temperature increases, CO emissions gradually stabilize at lower emission levels, because in the state of high heat flux density, volatiles are easily emitted and completely burned [26]. It can also be seen that the average overflow rate of CO increased first after declining; a tendency also noted in the research of Tang [27]. The maximum average emission rate (808.95 ppmv/s) was 113 times as large as the minimum rate (7.16 ppmv/s). In this paper, the average overflow rate of CO reached its peak value at 873 K, indicating once again that 873 K was the excessive temperature from incomplete combustion to complete combustion.

Volume Reduction Rate
The volume reduction rate and average weight loss rate of soybean straw under different temperature levels are shown in Figures 4 and 5, respectively. As the temperature rose, their values increased. The weight loss was mainly carried out at temperatures below 873 K, which matched up to the research of cellulosic material combustion [23]. It might be owed to devolatilization of lignocellulose and fixed carbon combustion [28], for the volatile and fixed carbon can reach up to  As seen from Table 2, the output time of CO is brought forward with a rise of temperature, and the maximum extent is about 7 s. It is made clear that volatile overflowed more easily. It should be on this account that the output of volatile is in close relation to heat flux [24]. From the point of view of heat transport, with higher combustion temperature, the material has a larger thermal gradient and heat flux from inside to outside, and its temperature rose more rapidly to improve the material drying degree and volatile precipitation. From the point of view of mass transfer, under low-temperature levels, pyrolysis plays a major role in the initial stage of combustion, whereas a large amount of coke formed by incomplete pyrolysis in the outer layer of material, which will have reactions with the overflow of volatile and even block the volatile [25]. In addition, the CO reached its maximum emission level at 221 s. As the temperature increases, CO emissions gradually stabilize at lower emission levels, because in the state of high heat flux density, volatiles are easily emitted and completely burned [26]. It can also be seen that the average overflow rate of CO increased first after declining; a tendency also noted in the research of Tang [27]. The maximum average emission rate (808.95 ppmv/s) was 113 times as large as the minimum rate (7.16 ppmv/s). In this paper, the average overflow rate of CO reached its peak value at 873 K, indicating once again that 873 K was the excessive temperature from incomplete combustion to complete combustion.

Volume Reduction Rate
The volume reduction rate and average weight loss rate of soybean straw under different temperature levels are shown in Figures 4 and 5, respectively. As the temperature rose, their values increased. The weight loss was mainly carried out at temperatures below 873 K, which matched up to the research of cellulosic material combustion [23]. It might be owed to devolatilization of lignocellulose and fixed carbon combustion [28], for the volatile and fixed carbon can reach up to 83.81% of material proximate analysis. When the temperature was higher than 873 K, the volume reduction was relatively small, and the increasing range of volume reduction rate was only 2.31%. 83.81% of material proximate analysis. When the temperature was higher than 873 K, the volume reduction was relatively small, and the increasing range of volume reduction rate was only 2.31%.  From 873 to 1173 K, the weight loss can be related to the reduction reaction of semicoke with CO2 [28,29] and degradation of minerals [30]. However, the average weight loss rate rose as the combustion temperature increased, indicating that high temperature is quite advantageous to rapid volume reduction of material. Moreover, 873 K was the inflection temperature of the average weight loss rate. The average weight loss rate at 973, 1073, and 1173 K increased by 27.38%, 61.47% and 77.97%, respectively, relative to that of 873 K; it stood to reason that complete combustion could promote volatile to separate out, cause the flammable substance to break down, and raise the combustion efficiency [31]. Figure 6 shows the NOX emission concentration under different temperatures. As shown in the figure, the NOX peak concentration increased as temperature rose, and the time to reach peak concentration shortened. The most conspicuous difference occurred between 873 and 973 K; within that range the peak concentration increased 63.75%, and the time to reach peak concentration was reduced by 143 s. Combined with the analysis of CO emission, it is clear that NOX formation has a strong relation to combustion temperature and combustion state [32][33][34]. 83.81% of material proximate analysis. When the temperature was higher than 873 K, the volume reduction was relatively small, and the increasing range of volume reduction rate was only 2.31%.  From 873 to 1173 K, the weight loss can be related to the reduction reaction of semicoke with CO2 [28,29] and degradation of minerals [30]. However, the average weight loss rate rose as the combustion temperature increased, indicating that high temperature is quite advantageous to rapid volume reduction of material. Moreover, 873 K was the inflection temperature of the average weight loss rate. The average weight loss rate at 973, 1073, and 1173 K increased by 27.38%, 61.47% and 77.97%, respectively, relative to that of 873 K; it stood to reason that complete combustion could promote volatile to separate out, cause the flammable substance to break down, and raise the combustion efficiency [31]. Figure 6 shows the NOX emission concentration under different temperatures. As shown in the figure, the NOX peak concentration increased as temperature rose, and the time to reach peak concentration shortened. The most conspicuous difference occurred between 873 and 973 K; within that range the peak concentration increased 63.75%, and the time to reach peak concentration was reduced by 143 s. Combined with the analysis of CO emission, it is clear that NOX formation has a strong relation to combustion temperature and combustion state [32][33][34]. From 873 to 1173 K, the weight loss can be related to the reduction reaction of semicoke with CO 2 [28,29] and degradation of minerals [30]. However, the average weight loss rate rose as the combustion temperature increased, indicating that high temperature is quite advantageous to rapid volume reduction of material. Moreover, 873 K was the inflection temperature of the average weight loss rate. The average weight loss rate at 973, 1073, and 1173 K increased by 27.38%, 61.47% and 77.97%, respectively, relative to that of 873 K; it stood to reason that complete combustion could promote volatile to separate out, cause the flammable substance to break down, and raise the combustion efficiency [31]. Figure 6 shows the NO X emission concentration under different temperatures. As shown in the figure, the NO X peak concentration increased as temperature rose, and the time to reach peak concentration shortened. The most conspicuous difference occurred between 873 and 973 K; within that range the peak concentration increased 63.75%, and the time to reach peak concentration was reduced by 143 s. Combined with the analysis of CO emission, it is clear that NO X formation has a strong relation to combustion temperature and combustion state [32][33][34]. NOX total emission, under different temperature levels, is shown in Figure 7. The occurrence time of NOX advances with the increase of temperature. After the temperature is higher than 873 K, there is a large span advance. When the temperature was 973, 1073, and 1173 K, the output time was moved forward by 102, 110, and 119 s, respectively, compared to 873 K. It seems that NOX formation could be related to combustion temperature [35]. However, the total emission of NOX increased first and reduced afterward, reaching its peak value (10,875 ppmv) at 873 K, increasing to about 46.11% of the total emission (7443 ppmv) at 1173 K; according to previous studies, possibly because at high temperature the catalysis of alkaline earth metal oxide reduces the NOX [36,37]. On the other hand, the reaction between NOX and CO is shown in Equations (10) and (11). The main products are N2 and N2O. The products in the high-temperature range are mainly N2 [26,38]. At the same time, a large amount of volatiles will overflow at high temperatures. A large number of carbon pore structures are produced, which makes NOX more likely to contact coke [39,40], and the reaction Equation (12) consumes some NOX, resulting in a reduction in the total amount of NOX.  NO X total emission, under different temperature levels, is shown in Figure 7. The occurrence time of NO X advances with the increase of temperature. After the temperature is higher than 873 K, there is a large span advance. When the temperature was 973, 1073, and 1173 K, the output time was moved forward by 102, 110, and 119 s, respectively, compared to 873 K. It seems that NO X formation could be related to combustion temperature [35]. However, the total emission of NO X increased first and reduced afterward, reaching its peak value (10,875 ppmv) at 873 K, increasing to about 46.11% of the total emission (7443 ppmv) at 1173 K; according to previous studies, possibly because at high temperature the catalysis of alkaline earth metal oxide reduces the NO X [36,37]. On the other hand, the reaction between NO X and CO is shown in Equations (10) and (11). The main products are N 2 and N 2 O. The products in the high-temperature range are mainly N 2 [26,38]. At the same time, a large amount of volatiles will overflow at high temperatures. A large number of carbon pore structures are produced, which makes NO X more likely to contact coke [39,40], and the reaction Equation (12) consumes some NO X, resulting in a reduction in the total amount of NO X .

Power Consumption
3C + 4NO = CO 2 + 2CO + 2N 2 (11) 2CO + 2NO = 2CO 2 + N 2 (12) Energies 2020, 13, x FOR PEER REVIEW 7 of 12 NOX total emission, under different temperature levels, is shown in Figure 7. The occurrence time of NOX advances with the increase of temperature. After the temperature is higher than 873 K, there is a large span advance. When the temperature was 973, 1073, and 1173 K, the output time was moved forward by 102, 110, and 119 s, respectively, compared to 873 K. It seems that NOX formation could be related to combustion temperature [35]. However, the total emission of NOX increased first and reduced afterward, reaching its peak value (10,875 ppmv) at 873 K, increasing to about 46.11% of the total emission (7443 ppmv) at 1173 K; according to previous studies, possibly because at high temperature the catalysis of alkaline earth metal oxide reduces the NOX [36,37]. On the other hand, the reaction between NOX and CO is shown in Equations (10) and (11). The main products are N2 and N2O. The products in the high-temperature range are mainly N2 [26,38]. At the same time, a large amount of volatiles will overflow at high temperatures. A large number of carbon pore structures are produced, which makes NOX more likely to contact coke [39,40], and the reaction Equation (12) consumes some NOX, resulting in a reduction in the total amount of NOX.

Power Consumption
Energy consumption can be regarded as an important index [41][42][43]. The effect of combustion temperature on power consumption is shown in Table 3. As shown in the table, when the temperature rose, the time of the experiment test expanded, and the maximum range was 58.315%. The cause was that when the set combustion temperature was higher, more heating-up time was required [44]. It was the efficient cause of the increased power consumption; the maximum (1.709 kWh) was 4.222 times as high as the minimum (0.405 kWh). However, during the experiment, the energy consumption cost from the heating period accounts for more than half of the total power consumption. With the continuous improvement of the temperature, the proportion of W r can reach 88.456%. This may be due to the small amount of experimental materials used, resulting in low power consumption cost during combustion. It is apparent that the power consumption during experiment preparation cannot be ignored, and it has a high impact on energy loss analysis of the experiment.

Optimum Combustion Temperature
The CO, NO X and volume reduction rate increment of unit power consumption in different combustion temperatures are shown in Figures 8-10.
In the range 773-873 K, the total emission of CO and NO X increased as energy input; the increments were 411046.1 and 49.8 ppmv/kWh, respectively. It seems that this temperature stage is inadvisable because it consumes more energy and produces more pollutants synchronously. However, during each temperature stage which was higher than 873 K, the total emission of unit power consumption of CO and NO X decreased, and the maximum decrements (857023.6 and 59.2 ppmv/kWh, respectively) were carried out in 873-973 K, indicating that in this temperature stage combustion ran to its complete state, and NO X emission reduced quickly at the same time. It is of great benefit to save energy and protect the environment.
Energies 2020, 13, x FOR PEER REVIEW 8 of 12 Energy consumption can be regarded as an important index [41][42][43]. The effect of combustion temperature on power consumption is shown in Table 3. As shown in the table, when the temperature rose, the time of the experiment test expanded, and the maximum range was 58.315%. The cause was that when the set combustion temperature was higher, more heating-up time was required [44]. It was the efficient cause of the increased power consumption; the maximum (1.709 kWh) was 4.222 times as high as the minimum (0.405 kWh). However, during the experiment, the energy consumption cost from the heating period accounts for more than half of the total power consumption. With the continuous improvement of the temperature, the proportion of can reach 88.456%. This may be due to the small amount of experimental materials used, resulting in low power consumption cost during combustion. It is apparent that the power consumption during experiment preparation cannot be ignored, and it has a high impact on energy loss analysis of the experiment.

Optimum Combustion Temperature
The CO, NOX and volume reduction rate increment of unit power consumption in different combustion temperatures are shown in Figures 8,9,and 10. In the range 773-873 K, the total emission of CO and NOX increased as energy input; the increments were 411046.1 and 49.8 ppmv/kWh, respectively. It seems that this temperature stage is inadvisable because it consumes more energy and produces more pollutants synchronously. However, during each temperature stage which was higher than 873 K, the total emission of unit power consumption of CO and NOX decreased, and the maximum decrements (857023.6 and 59.2 ppmv/kWh, respectively) were carried out in 873-973 K, indicating that in this temperature stage combustion ran to its complete state, and NOX emission reduced quickly at the same time. It is of great benefit to save energy and protect the environment.  As seen in Figure 10, the volume reduction rate increment of unit power consumption during 773-873 K had a maximum value of 18.304%/kWh. However, when the experiment entered the next three temperature stages of 873-973, 973-1073, and 1073-1173 K, the relevant value sharply declined to 4.504%, 2.871% and 0.127%/kWh, respectively. It meant that when the temperature was higher than 873 K, the material volume lessens little with the power input. Therefore, a temperature higher than 873 K should be selected in order to reduce the volume to a large extent. According to the analysis, it seems that the temperature stage of 873-973 K is of great benefit to lower CO and NOX emission, and the residual mass remained basically stable. So 873-973 K seems to be propitious to high efficiency and low emission combustion of soybean straw.

Conclusions
An experimental investigation on soybean straw combustion was performed to determine a balance of temperature impact on both energy consumption and environmental protection. Then, the emission and combustion characteristics of soybean straw were compared at different temperatures. Results show that the pollutants such as CO and NOX from soybean straw combustion at 873 K are higher than other temperatures. CO reached its maximum total emission as 354,570 ppmv at 873 K, which was 195 times as large as it was at 1173 K. The NOX at 873 K had its maximum total emission 10,875 ppmv, which was 53.018% higher than the minimum of 7107 ppmv at 1173 K. The volume As seen in Figure 10, the volume reduction rate increment of unit power consumption during 773-873 K had a maximum value of 18.304%/kWh. However, when the experiment entered the next three temperature stages of 873-973, 973-1073, and 1073-1173 K, the relevant value sharply declined to 4.504%, 2.871% and 0.127%/kWh, respectively. It meant that when the temperature was higher than 873 K, the material volume lessens little with the power input. Therefore, a temperature higher than 873 K should be selected in order to reduce the volume to a large extent.
Energies 2020, 13, x FOR PEER REVIEW 9 of 12 Figure 9. NOX increment of unit power consumption in different temperature phases.
As seen in Figure 10, the volume reduction rate increment of unit power consumption during 773-873 K had a maximum value of 18.304%/kWh. However, when the experiment entered the next three temperature stages of 873-973, 973-1073, and 1073-1173 K, the relevant value sharply declined to 4.504%, 2.871% and 0.127%/kWh, respectively. It meant that when the temperature was higher than 873 K, the material volume lessens little with the power input. Therefore, a temperature higher than 873 K should be selected in order to reduce the volume to a large extent. According to the analysis, it seems that the temperature stage of 873-973 K is of great benefit to lower CO and NOX emission, and the residual mass remained basically stable. So 873-973 K seems to be propitious to high efficiency and low emission combustion of soybean straw.

Conclusions
An experimental investigation on soybean straw combustion was performed to determine a balance of temperature impact on both energy consumption and environmental protection. Then, the emission and combustion characteristics of soybean straw were compared at different temperatures. Results show that the pollutants such as CO and NOX from soybean straw combustion at 873 K are higher than other temperatures. CO reached its maximum total emission as 354,570 ppmv at 873 K, which was 195 times as large as it was at 1173 K. The NOX at 873 K had its maximum total emission 10,875 ppmv, which was 53.018% higher than the minimum of 7107 ppmv at 1173 K. The volume According to the analysis, it seems that the temperature stage of 873-973 K is of great benefit to lower CO and NO X emission, and the residual mass remained basically stable. So 873-973 K seems to be propitious to high efficiency and low emission combustion of soybean straw.

Conclusions
An experimental investigation on soybean straw combustion was performed to determine a balance of temperature impact on both energy consumption and environmental protection. Then, the emission and combustion characteristics of soybean straw were compared at different temperatures. Results show that the pollutants such as CO and NO X from soybean straw combustion at 873 K are higher than other temperatures. CO reached its maximum total emission as 354,570 ppmv at 873 K, which was 195 times as large as it was at 1173 K. The NO X at 873 K had its maximum total emission 10,875 ppmv, which was 53.018% higher than the minimum of 7107 ppmv at 1173 K.
The volume reduction rate at 1173 K was only 2.31% higher than that at 873 K. Furthermore, the time to reach the peak NO X emission concentration at 973 K was 143 s faster than at 873 K. The higher temperature keeps the soybean straw in a complete state of combustion, which avoids excessive CO and inhibits the generation of NO X . However, the additional energy consumption caused by the increased temperature needs to be considered in the test. All the power consumption during the temperature-rise period was over 60% of the total power consumption. Therefore, the soybean straw combustion temperature of 873-973 K is recommendable as a comprehensive consideration of energy consumption and environmental protection.