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Abstract
Seaweed has attracted considerable attention as a potential biofuel feedstock. The pyrolytic and kinetic characteristics of maize straw and the seaweed Ulva pertusa were studied and compared using heating rates of 10, 30 and 50°C min−1 under an inert atmosphere. The activation energy, and pre-exponential factors were calculated by the Flynn-Wall-Ozawa (FWO), Kissinger-Akahira-Sunose (KAS) and Popescu methods. The kinetic mechanism was deduced by the Popescu method. The results indicate that there are three stages to the pyrolysis; dehydration, primary devolatilization and residual decomposition. There were significant differences in average activation energy, thermal stability, final residuals and reaction rates between the two materials. The primary devolatilization stage of U. pertusa can be described by the Avramic-Erofeev equation (n = 3), whereas that of maize straw can be described by the Mampel Power Law (n = 2). The average activation energy of maize straw and U. pertusa were 153.0 and 148.7 KJ mol−1, respectively. The pyrolysis process of U.pertusa would be easier than maize straw. And co-firing of the two biomass may be require less external heat input and improve process stability. There were minor kinetic compensation effects between the pre-exponential factors and the activation energy.
Citation: Ye N, Li D, Chen L, Zhang X, Xu D (2010) Comparative Studies of the Pyrolytic and Kinetic Characteristics of Maize Straw and the Seaweed Ulva pertusa. PLoS ONE 5(9): e12641. https://doi.org/10.1371/journal.pone.0012641
Editor: Matthew H. Todd, University of Sydney, Australia
Received: April 21, 2010; Accepted: August 15, 2010; Published: September 10, 2010
Copyright: © 2010 Ye et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the National Natural Science Foundation of China (40706050, 40706048 and 30700619), the National Science & Technology Pillar Program (2006BAD01A13 and 2008BAC49B04), National special fund for transgenic project (2009ZX08009-019B), Natural Science Foundation of Shandong Province (2009ZRA02075), Qingdao Municipal Science and Technology plan project (09-2-5-8-hy) and the Hi-TechResearch and Development Program (863) of China (2006AA10Z414). Funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
In recent years, marine origin biomass such as seaweed, has attracted considerable attention as a potential biofuel feedstock. Seaweeds are an important component in marine ecosystems providing an important and unique ecological function. As a potential biofuel feedstock, macroalgae seaweeds have a number of desirable features, such as fast growth, high biomass conversion rate, short growth cycle, ease of handling and the potential for zero net CO2 emissions.
Pyrolysis can be used to harvest the energy contained in macroalgae. The technique has been previously proposed and the pyrolytic characteristics of macroalgae have been examined [1]–[5]. However, the product yield from pyrolysis is still very low and the resulting bio-oils have many complex components which can be corrosive or hygroscopic [1]. Thus, to produce a practical process route further study of the pyrolytic characteristics of macro-algae is required.
Ulva pertusa is native to China and exhibits fast growth and a high reproductive capacity. The alga differs from higher plants, by having a cell wall comprises of two layers, the inner layer is composed of cellulose and the external layer is composed of pectin which in turn consists of D-galactose, L-alabinose, D-xylose and an L-rhamnose complex on the cell surface [6]. U. pertusa is a green algae. In terms of cell wall construction and biochemical elements, these green algae most closely resemble higher plants.
Chinese agriculture is producing huge amount of maize straw as a by-product [7]. Maize straw can be used for pyrolytic oil production using recently developed technologies such as fast pyrolysis [8].
In this study, maize straw is chosen as a representative of terrestrial crops composed of hemicelluloses, cellulose and lignin, to compare to U. pertusa in terms of pyrolytic and kinetic characteristics. The average activation energy, pre-exponential factors, and reaction orders associated with pyrolysis were calculated to facilitate the efficient design, operation, and modeling of pyrolytic and related thermo-chemical conversion systems for both algae and higher plants.
Results and Discussion
Characteristics of the thermal degradation process
As previous studies [1]–[2], thermogravimetric (TG) (Fig. 1) and differential thermogravimetric (DTG) (Fig. 2) curves of maize straw and U. pertusa indicated that there are three stages in the pyrolytic process. The first stage (I) occurred as the temperature increased from ambient to T1, while the second stage (II) occurred as the temperature increased from T1 to T5. However, the samples revealed large differences in degradation behavior during stage II. Stage II was composed of two zones for maize straw, with zone I occurring as the temperature increased from T1 to T3 with a maximum weight loss point at T2 and zone II occurring as the temperature increased from T3 to T5 with a maximum weight loss point at T4. For U. pertusa, there was only one zone in stage II, which occurred as the temperature increased from T1 to T5 with a maximum weight loss point at T3. The third stage (III) occurred as the temperature increased from T5 to 800°C. The characteristic temperatures are shown in Table 1 and Fig. 2.
Fu et al. (2008) [9] indicated that the maize straw showed a DTG curve with a single peak and a shoulder. However, Muller-Hagedorn et al. (2007) [10] found that the two maize samples in their studies showed only one wide DTG curve peak. Normally, DTG curves from biomass exhibit a peak at high temperatures that is mainly due to the pyrolysis of the cellulose and a shoulder at lower temperatures that can be attributed to the pyrolysis of the hemicelluloses [10]. A previous study of green algae by our research group [1] showed DTG curves with one wide peak for Enteromorpha prolifera, as well as U. pertusa.
During stage I, cellular water and the external water bound by surface tension are lost. Stage II is the devolatilization stage, during which the main pyrolytic process occurs. In this stage, various volatile components are gradually released, resulting in a large weight loss and formation of the main pyrolytic products. Stage II occurred over a temperature range of 200–408°C for maize straw and 182.3–316°C for U. spertusa. The onset of decomposition occurs at a lower temperature for U. pertusa than for maize straw. This may be caused by the low polymerization of the polysaccharides and the presence of inorganic salts in U. pertusa [2], [5]. During the third stage, the residue slowly decomposed, resulting in the formation of a loose porous product.
The weight loss is seen in the three samples during stage I (Table 2) were primarily due to the loss of moisture and were similar to the moisture content values reported in Table 3. The amount of the final residue of maize straw at 800°C was lower than U. pertusa. In addition, the instantaneous maximum reaction rate for maize straw was higher than U. pertusa. For maize straw, the instantaneous maximum reaction rate occurred in zone II of stage II.
Heating rate has significant effect on the pyrolysis of maize straw and U. pertusa. As the heating rate increased, the initial pyrolytic temperature, the average reaction rate and the temperature at which the maximum weight loss occurred, all increased (Tables 1 and 2).
As the heating rate increased, the reaction exotherm also increased (Fig. 3). There was an endothermic peak during stage I that corresponded with moisture evaporation. As the temperature increased, an exothermic effect appeared during stage II and exothermic peaks were observed at 5–15°C after the maximum weight loss point. These findings indicate that the devolatilization stage (stage II) produced heat. Moreover, as the temperature continued to rise, there were differences among the differential scanning calorimetry (DSC) curves produced using different heating rates. Specifically, there was an endothermic effect during the maize straw stage III. There was also an exothermic effect during stage III when heating rates of 50°C/min were used for U. pertusa.
1 is the DSC curve of maize straw at heating rate of 10°C/min; 2 is the DSC curve of maize straw at heating rate of 30°C/min; 3 is the DSC curve of maize straw at heating rate of 50°C/min; 4 is the DSC curve of U. pertusa at heating rate of 10°C/min; 5 is the DSC curve of U. pertusa at heating rate of 30°C/min; 6 is the DSC curve of U. pertusa at heating rate of 50°C/min.
An endothermic maximum peak corresponding to the maximum weight loss rate peak appeared on the maize straw DSC curve (Fig. 4A). However, the highest exothermic peak appeared on the DSC curve of U. pertusa (Fig. 4B). This suggests that the pyrolysis of U. pertusa is mainly an exothermic process. Generally speaking, an endotherm can be related to depolymerization and volatilization processes, whereas an exotherm is due to charring [3], [11]. This may be caused by the low depolymerization energy requirement and inorganic salts present in U. pertusa assisting in robust char formation and exothermic effects [2], [11].
Kinetic analysis of the pyrolysis process
Popescu method for determining the kinetic mechanism.
Different conversion rates in stage II at different heating rates and temperatures were chosen to determine the mechanism function (Table 4). Forty-one typical mechanisms [12] were analyzed using the Popescu method. Table 4 shows correlation coefficients (R) and standard deviations (SD).
As shown in Table 4, function 19 () is the best fit function for U. pertusa (n = 3), while function 27 (
) is the best fit function for maize straw (n = 2). For U. pertusa, the most probable mechanism may be interpreted as random nucleation and nuclei growth. At first, the decomposition reaction occurred on partional point of solid phase and activation center generated randomly. Thereafter, partial activation center produce decomposition product or inactivated, and partial activation center contnuning to grow followed by newly formed activation center. For maize straw, the most probable mechanism was nucleation.
Wang et al. [3] and Li et al.[2] found that random nucleation and growth was predominant during the main pyrolysis of algae, which is described by the Amirami-Erofeev function. We obtained similar results (n = 3) to the mechanism proposed for L. japonica and S. pallidum [2].
Maize straw was mainly composed by lignocellulosic material (approximately for 80%). However, Ulva pertusa were mainly composed of protein, polysaccharides and little cellulose. Moreover, large amount of inorganic salts in seaweeds may be the other reaons which can induce the heterogeneous nucleation of the volatile [3]. The different mechanisms of maize straw and U. pertusa may be the result of differing sample compositions and the physical configuration of the powder.
Calculation of the activation energy and pre-exponential factors.
The activation energy and lnA of maize straw and U. pertusa are listed in table 5. The results have confidence values ranging from 0.9179 to 0.99999. Therefore, the activation energy calculated by the Popescu method, FWO and the KAS methods are valid. However, the activation energy revealed fluctuations related to conversion rates. This may be ascribed to the complex composition of the samples and the complex reactions that occur during pyrolysis. For maize straw, the rank order of the activation energies calculated by the different methods are Popescu method, FWO method and KAS method. However, for U. pertusa, the order is FWO method, KAS method and Popescu method. It also indicates that the activation energy calculated by the FWO method is always higher than from the KAS method. The average activation energy of U. pertusa (148.7 KJ/mol) was lower than maize straw (153.0 KJ/mol), indicating that U.pertusa caught fire easily than maize straw. However, the lnA values of U.pertusa were higher than that of maize straw which indicated that the pyrolysis process of the former would be easier than the latter. This suggested that co-firing of the two biomass may be require less external heat input and improve process stability. The activation energy distribution of U.pertusa were wider than maize straw.
Comparisons of the decomposition temperature and activation energy of several types of biomass are provided in Table 6 [1], [2], [13], [14], [15]. The results indicated that the decomposition temperature of algae is lower than that of the higher plants, however the activation energies do differ. These findings suggest that thermal behavior is greatly influenced by feedstock choice.
Table 7 shows the kinetic compensation effects of the pre-exponential factors and activation energies. In addition to the pre-exponential factors and the activation energy calculated by Popescu methods of U. pertusa, there were minor kinetic compensation effects between the pre-exponential factors and the activation energies.
Conclusions
The pyrolysis of biomass can be influenced by the choice of biomass type, pyrolytic temperature, and heating rate. Therefore, the pyrolytic characteristics and kinetics need to be studied for each type of biomass under consideration as feedstock, prior to designing thermal-chemical conversion systems.
Our studies found that there were three stages during the pyrolysis of maize straw and U. pertusa which were distinguished as moisture evaporation (stage I), a main pyrolysis process (stage II) and a slow decomposition process (stage III). However, there are significant differences between stages for the different materials. U. pertusa is easier to pyrolyse than maize straw. There is more residue from the pyrolysis of U. pertusa than from maize straw, indicating that the inorganic salts should be washed out of U. pertusa before use as a pyrolysis feedstock.
In addition, there are differences between pyrolysis mechanisms. The primary devolatilization stage of U. pertusa can be described by Avramic-Erofeev equation (n = 3), whereas that of maize straw can be described by Mampel Power Law (n = 2).
Further investigation of pyrolysis products is required to fully understand the mechanisms of thermal degradation of the two samples.
Materials and Methods
Sample preparation
U. pertusa was collected in June of 2009 from the Zhanqiao piers in Qingdao, China. Dry maize straw was collected from the maize planting regions surrounding Liaocheng, Shandong province, China. U. pertusa was sun dried for four days, after which both the U. pertusa and the dry maize straw were pulverized in a plant disintegrator to all passing a 120 mesh sieve. All samples were stored in a desiccator.
Proximate analysis of the samples
The moisture analysis was conducted according to established methods [16]. The ash content was determined according to the method described in [17]. The volatile matter content was analyzed according to the method described in [18]. The fixed carbon was expressed as the 100%-ash content-volatile matter-moisture content. Calorific values were determined according to the method described in [19]. All measurements were replicated three times.
Pyrolysis of the samples
The pyrolytic characteristics were determined according to Li et al. (2010) [2]. Ten milligrams of the sample were put into platinum crucibles with lids on a high accuracy DSC-cp sample holder of a thermal analyzer (TG/DSC STA449, NETZSCH Instruments Co. Ltd., Germany), after which they were heated from ambient temperature to 800°C at rates of 10, 30 and 50°C/min in the furnace under a nitrogen atmosphere of 80 ml/min. The weight loss and calorific changes in response to temperature were then recorded and used to plot the thermogravimetric analysis (TGA), derivative thermogravimetric analysis (DTG) and differential scanning calorimetric (DSC) curves. All experiments were replicated three times.
The kinetic parameters of the samples
The most probable mechanism was determined by the Popescu method [20], [2], and the activation energy and pre-exponential factor were calculated by using the Popescu method [20], [2], FWO method [21]–[22], [1]–[2] and KAS method [23], [2].
All plots were generated and the lines were fitted using the Origin 7.5 software package (OriginLab Corporation).
Author Contributions
Conceived and designed the experiments: NY. Performed the experiments: DL LC. Analyzed the data: LC XZ DX. Contributed reagents/materials/analysis tools: NY. Wrote the paper: NY DL.
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