Research Article  Open Access
A Kinetic Study of Marginal Soil Energy Plant Helianthus annuus Stalk Pyrolysis
Abstract
The pyrolytic characteristics and kinetics of new marginal soil energy plant Helianthus annuus stalk were investigated using thermogravimetric (TG) method from 50 to 800°C in an inert argon atmosphere at different heating rates of 5, 10, 20, and 30°C min^{−1}. The kinetic parameters of activation energy and preexponential factor were deduced by Popescu, FlynnWallOzawa (FWO), and KissingerAkahiraSunose (KAS) methods, respectively. The results showed that three stages appeared in the thermal degradation process. The primary devolatilization stage of H. annuus stalk can be described by the AvramiErofeev function . The average activation energy of H. annuus stalk was only 142.9 kJ mol^{−1}. There were minor kinetic compensation effects between the preexponential factor and the activation energy. The results suggest that H. annuus stalk is suitable for pyrolysis, and more importantly, the experimental results and kinetic parameters provided useful information for the design of pyrolytic processing system using H. annuus stalk as feedstock.
1. Introduction
As potential “next generation” biofuel feedstock, marginal soil plants have attracted considerable attention because of their advantages, such as high photosynthetic efficiency, maximum biomass production, fast growing, high conversion rate, ease of harvesting, and lack of arable soil requirements. Helianthus annuus can grow well in barren marginal lands and has good resistance to adverse situations. Moreover, it does not compete with grain crops for arable lands, which is significant for one populous country lack of arable land as China. The agriculture is producing huge amount of H. annuus stalks as byproducts of seeds every year in China. It has been reported that the stalk yield was ranging between 5 and 14 tons per hectare. H. annuus has an excellent adaptability, and the growth cycle is only about 100 days. These characteristics of H. annuus suggest that it can be used as a good potential energy source and should be further studied as a good biofuel feedstock candidate [1–8].
Biomass pyrolysis has demonstrated itself to be a kind of biomassenergy utilization technology which transforms lowenergy density biomass materials into highenergy density liquid products which can be utilized more efficiently in an environmentfriendly manner. A thorough knowledge of the thermal behavior and pyrolysis kinetics of biomass are required for the proper design and operation of the pyrolysis conversion systems. Thermogravimetry (TG) analysis method was selected to investigate the thermal decomposition process. The kinetic data from TG are not only very useful for understanding the thermal degradation processes and mechanisms, but also can be used as input parameters for a thermal degradation reaction system [9–11].
In present study, H. annuus stalk pyrolysis was investigated using a TG/DSC instrument with nonisothermal thermogravemetric (TG) analysis method at different heating rates under an inert atmosphere. The pyrolysis characteristics and kinetics were examined by Popescu, FlynnWallOzawa (FWO) and KissingerAkahiraSunose (KAS) methods and then the average activation energy, preexponential factors, and reaction orders were deduced. The objective of this study was to obtain the kinetic parameters of thermal decomposition and then to determine the degradation mechanism for facilitating the efficient design, operation, and modeling of pyrolysis and related thermochemical conversion systems for energy plants.
2. Materials and Methods
2.1. Materials
H. annuus stalk was collected from the marginal land of Shandong University of Science and Technology campus, Qingdao, China, January 2012. Sample was dried in one drying oven at 100 ± 2°C for 10 hours and pulverized in a plant disintegrator to be able to pass through a 120mesh sieve, and then stored in a desiccator.
2.2. Proximate and Component Analysis of the Sample
Proximate analysis was carried out according to the national standard GB21291 (China). For analysis of composition, the biomass materials were hydrolyzed using 72%, 2 mol/L HCl and concentrated HCl to analyze cellulose, hemicellulose and lignin contents according to established methods, respectively [10, 12, 13]. The results were presented in Table 1. All tests were carried out in triplicate.
 
^{
a}Mass percentage on asreceived basis; ^{b}calculated by difference. 
2.3. Pyrolysis by Thermogravimetric Analyzer
Pyrolytic characteristics were determined by using a thermal analyzer (TGA/DSC1/1600LF Mettler Toledo Co., Switzerland). In the experiment, argon gas was used as a carrier gas with a flow rate of 50 cm^{3} min^{−1}. The heating rate was controlled at 5, 10, 20, 30°C min^{−1} from 50 to 800°C. The sample mass that was used for the thermogravimetric analysis in each experiment was 10 mg approximately. Mass loss and calorific changes in response to temperature were recorded and used to plot thermogravimetric (TG), derivative thermogravimetric analysis (DTG), and differential scanning calorimetric (DSC) curves [14, 15]. All experiments were replicated three times. The software Origin 8.0 was used to analyze the data and plot the curves.
2.4. Kinetic Analysis
2.4.1. Popescu Method
The Popescu method was used to evaluate the most probable mechanism of the pyrolytic reaction [12, 13]. In other words, the Arrhenius equation was selected to analyze the thermal decomposition reactions. The dynamic equation is: where is the conversion rate and is defined as follows: and here, , , are the initial, actual, and the end mass of samples, mg;
where is the velocity constant, and is the differential coefficient mechanism function.
Consider
thus, with the combination of (1), (2), and (3), the rate of a solidstate reaction can generally be described by:
and then, if the temperature is controlled at a constant heating rate, . Therefore, (4) gives:
Then the integral form of (5) is: For this equation, where , are two different degrees of conversion, and , are their corresponding temperatures, and here , and can be described as follows, respectively:
Therefore, a plot of versus gives a straight line with an intercept of zero. If the experiment data and are chosen properly, a plot of versus gives a straight line with an intercept of zero. Then, this is the proper mechanism that can express the true chemical reaction process.
By logarithmic transformation of (6), a linear equation is deduced:
A plot of versus gives a straight line with a slope of and intercept of . Therefore, and can be determined.
2.4.2. FWO and KAS Method
It is well known that flynnwallozawa (FWO) method and kissingerakahirasunose (KAS)method were generally used to deduce the activation energy and preexponential factor, and the apparent activation energy is influenced by temperature and fractional conversion [13, 16–20]. So, activation energy can be obtained with the change of heating rate .
FlynnWallOzawa equation:
KAS equation:
According to (9) and (10), plots of , versus with a certain conversion rate give straight lines with slopes of , and the activation energy can be determined. Then, the activation energy () can be determined. Substituting the value of and the mechanism function back into (9) and (10) in conjunction with and , can be calculated.
3. Results and Discussion
3.1. Characteristics of the Thermal Degradation Process
According to thermogravimetric (TG) and differential thermogravimetric (DTG) curves of H. annuus stalk (Figures 1 and 2), the results indicated that the pyrolysis process was made up of three stages. The stage I occurred as the temperature increased from room temperature to , while the second started as the temperature that increased from to (II). However, the sample revealed somewhat different during stage II. Stage II included two zones for H. annuus stalk pyrolysis process: zone I occurred as the temperature increased from to with a maximum mass loss point at , and zone II occurred as the temperature increased from to with a maximum mass loss point at . The last one, stage III occurred as the temperature increased from to 800°C. The concrete contents of the temperature characteristics were shown in Table 2 and Figure 2.

The TG and DTG curves of the sample at different heating rates (Table 2) and 20°C min^{−1} (Figures 1 and 2, all profiles of different heating rates are not presented here, and 20°C min^{−1} was shown as an example for concision) showed that three stages appeared corresponding to three different pyrolytic processes. The stage I was the process of slow mass loss corresponding to the evaporation of water and other volatile components, in other words, it is that both the internal cellular water and the external water bound by surface tension were lost [12]. From the Figure 2, stage II – was the devolatilization stage, during which the main pyrolytic process occurred. In this stage, various volatile components were gradually released, and biological macromolecules were depolymerized and fractured; that resulted in a large mass loss and formation of the main pyrolytic products. The temperature range of three samples during stage II was 130.4–272.5°C (H. annuus stalk) at different heating rates. During the stage III, the residual was slowly decomposed [26], resulting in the formation of a loose porous endproduct.
Heating rates have significant effects on the pyrolysis process. As the heating rate increasing, the mass loss rate and the average reaction rate both increased. The results were shown in Table 3.
 
^{
a}Mass loss,%; ^{b}Average reaction rate,%/min; ^{c}Zone I; ^{d}Zone II; ^{e}Final residual at 800°C,%. 
The differential scanning calorimetry (DSC) curves of three samples at different heating rates were presented in Figure 3. As the heating rate increasing, an obvious exothermic effect appeared, and this finding indicated that the pyrolysis process produced heat. During the stage I, there was an obvious endothermic peak, which corresponded to moisture evaporation. In stage II (devolatiliation stage), there were some differences among these three samples. As the temperature increased, H. annuus stalkmaintained the exothermic effect, while as the heating rate increasing, the exothermic effect became more obvious with the peak area increased. At the temperature of 400 to 500°C, there was an exothermic peak, which showed that the charring process occurred at this moment. Generally speaking, an endothermic process can be related to depolymerization and volatilization processes, while an exothermic process is due to charring. The pyrolysis had no clear endothermic effects, which suggested that the decomposition process needs low energy and the inorganic salts promote charring and exothermic effects.
3.2. Kinetic Analysis of the Pyrolysis Process
3.2.1. Determination of G(α)
Different conversion rates at different heating rates and temperatures were chosen to determine the pyrolysis mechanism function. These temperatures should be applied during stage II. The 41 kinds of typical mechanism functions [27] were analyzed according to the Popescu method to determine the function. And at last, according to these 41 kinds of typical mechanism functions, the function appeared as the most probable mechanism function for H. annuus stalk (Table 4). And then, the activation energy and preexponential factors can be calculated by function [28].
 
: Correlation coefficient; SD: standard deviation. 
3.2.2. Calculation of the Activation Energy and PreExponential Factors
According to (8), a plot of versus gives a straight line with a slope of and intercept of . Therefore, and can be determined. And on basis of (9) and (10), a plot of , against should be a linear relationship by FWO method and KAS method. Similarly, the activation energy and preexponential can be calculated (Figure 4). The values of activation energy and was listed in Table 5. The value of Square was close to 0.9500, that is to say, the values of coefficient of correlation were relatively high. So the values of activation energy deduced and calculated by Popescu, FWO, and KAS methods are valid. However, the values of activation energy increased with a different fluctuation at different conversion rates. This may be ascribed to the complex composition of the sample and the complex reactions during pyrolysis. In the end, the average activation energy value of H. annuus stalkwas 142.9 kJ mol^{−1}.
 
E: Activation energy; A: preexponential factor; R: correlation coefficient. 
(a)
(b)
(c)
In Table 6, various kinetic parameters of pyrolysis between different biomass sources were compared. Other results are not similar to the present study, which suggests that thermal behavior is influenced greatly by feedstock types [29].
In Table 7, the kinetic compensation effects of the preexponential factors and activation energy were shown. These results indicated that there was a partial compensation effect for when changed.

4. Conclusions
High priority should be given to the development and protection of biomass pyrolysis from new marginal soil energy plant with great potential, which is widely recognized as a technically feasible way for sustainability. In the present work, there were three stages in the process of H. annuus stalk pyrolysis, and stage II was the main pyrolysis process, and most of the organic materials were decomposed in this stage, and heating rates had a significant effect on the pyrolysis process of biomass.
The Popescu, FWO, and KAS methods were adopted to determine the kinetic parameters of the pyrolysis reaction. During the primary decomposition reactions, the most probable mechanism functions for H. annuus stalk was . The values of activation energy calculated by these three methods were similar. There was only a partial compensation effect for when changed. The results suggest that H. annuus stalk is suitable for pyrolysis, and more importantly, the experimental results and kinetic parameters provided useful information for the design of pyrolytic processing system using H. annuus stalk as feedstock.
Conflict of Interests
The authors declare that they have no conflict of interests.
Authors’ Contribution
H. Yan and H. Zhao participated in the design and coordination of the study, interpreted the data, and drafted and corrected the manuscript. Y. Zhang et al. participated in the interpretation of the data and corrected the draft paper. All authors read and approved the final paper.
Disclosure
H. Yan is a staff member of College of Chemical and Environmental Engineering, Shandong University of Science and Technology, Qingdao, China. Dr. H. Zhao is the leader of Biochemical Engineering and Bioresources Laboratory at College of Chemical and Environmental Engineering. His areas of specialization are biochemical engineering, energy, and environmental engineering. He has published over 10 papers in international journals. Y. Zhang is one master degree candidate. Y. Tian and K. Xie are the leaders of Key Laboratory of Lowcarbon Energy Chemical Engineering in Universities of Shandong, Shandong University of Science and Technology, Qingdao 266590, China, and contributed to supply the excellent research platform and guide research works.
Acknowledgments
This work was financially supported by National Natural Science Foundation of China (21076117, 41202165), Open Funding from the State Key Laboratory of Crop Biology in Shandong Agricultural University (2010KF06 and 2011KF14), Projects of Shandong Province Higher Educational Science and Technology Program (J10LC15), Open Project Program of Key Lab of Marine Bioactive Substance and Modern Analytical Technique (MBSMAT201203), and Qingdao Government Scientific and Technological Program.
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Copyright
Copyright © 2013 Huaxiao Yan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.