The Infiltration Process and Texture Transition of 2D C/C Composites

Transcription

1 J. Mater. Sci. Technol., Vol.25 No.1, The Infiltration Process and Texture Transition of 2D C/C Composites Hejun Li, Guozhong Xu, Kezhi Li, Chuang Wang, Wei Li and Miaoling Li Carbon/carbon Composites Research Center, Key Laboratory of Ultrahigh Temperature Composites, Northwestern Polytechnical University, Xi an , China [Manuscript received November 9, 2007, in revised form June 16, 2008] 2D needle-punched fiber felt was infiltrated by a kind of rapid isothermal chemical vapor infiltration technique. The infiltration process and texture transition of the infiltrated C/C composites were investigated. The porosity and the variations of the cumulative pore volume were determined by mercury porosimetry. The texture of matrix carbon was studied under a polarized light microscope. The results show that the relative mass gain of the sample increases directly as the infiltration time at the initial stage until 20 h, and subsequently the increasing rate of the relative mass gain decreases gradually with the prolonging of infiltration time. Three layers of pyrocarbon were formed around fibers. Low-textured pyrocarbon was obtained at the initial stage. With the densification going on, high-textured pyrocarbon was formed on the surface of low-textured pyrocarbon. Then, low-textured pyrocarbon was produced again during the final stage of densification. The texture transition is ascribed to the variation of the ratio of cumulative inner surface area to volume of pores and the gas partial pressure in pores. KEY WORDS: C/C composites; Isothermal chemical vapor infiltration (ICVI); Pyrocarbon; Mercury porosimetry; Polarized light microscope 1. Introduction Isothermal chemical vapor infiltration (ICVI) is currently a major process to produce carbon/carbon (C/C) composites. But this process has been considered to be strongly diffusion-limited since it was developed in the 1960s, which results in a long densification period [1,2]. To overcome this problem, some new techniques have been developed such as thermal gradient CVI [3,4], pulse CVI [5 7], forced flow thermal gradient CVI [8,9] and film boiling CVI [10,11]. However, these techniques cannot replace the ICVI process for mass production [12]. Therefore the study on the ICVI, which is mainly focused on the improvement of infiltration rate and control of texture structure, has never been ceased in recent years. In our previous work, the conventional ICVI furnace was improved, which reduced the densification period of ICVI to 125 h at ambient pressure using 2D needle-punched carbon felt as preform [13]. It has been found that the texture of the pyrocarbon around fibers changes abruptly even if the infiltration temperature, the total pressure, the partial pressure, and the residence time keep constant. This special phenomenon was also reported [12,14 16]. However, up to now, the reason for the abrupt change of the pyrocarbon texture has not been explained deeply. The aim of the present study was to analyze the infiltration process and the mechanism of the texture transition of pyrocarbon around fibers in detail. 2D needle-punched carbon felts were infiltrated by improved ICVI process at ambient pressure for different time. Natural gas was used as the precursor. The infiltration temperature, the partial pressure of methane and the residence time of gases were kept constant. The relative mass gain, accumulated pores Corresponding author. Prof.; Tel.: ; address: lihejun@nwpu.edu.cn (H.J. Li). volume and the ratio of cumulative inner surface area to volume of pores (As/Vr) of as-obtained samples as a function of densification time were systematically investigated. 2. Experimental 2.1 Preparation of C/C composites The preform used in the experiment was a kind of 2D needle-punched fiber felt, of which the volume percentage of carbon fibers was 28.7% and the architecture was 0 0 /90 0 /0 0 /90 0. The density of fibers was 1.72 g/cm 3. The pores are distributed among both fiber bundles and fiber layers as shown in Fig. 1. The preform size was 60 mm (height) 45 mm (length) 11 mm (thickness). According to the length of the felt, the infiltration depth amounts to 22.5 mm. Natural gas was used as precursor and the composition of the natural gas is shown in Table 1. Using nitrogen as the diluent Table 1 The composition of nature gas used in experiment Nature composition Volume percent/% CH C 2H C 3H C 4H CO H 2S 20 ml/m 3 H 2 and N 2 Trace gas, an improved infiltration furnace used in literature [12,17] was applied to manufacture C/C composites by a new technology [13,18]. The chemical vapor infiltration of the preforms was performed under ambient pressure. The infiltration time was varied by 5, 10, 15, 20, 25, 30, 50, 75, 100 and 125 h at a constant

2 110 J. Mater. Sci. Technol., Vol.25 No.1, Fig. 1 The image of 2D needle-punched fiber felt (m-m 0 )/ m 0 / % (m-m 0 )/m 0 / % Y= X R= Infiltration time, t / h Fig. 3 Relative mass gains of the preform as a function of the infiltration time 70 Porosity / % Sample 1B Sample 2B Fig. 2 The scheme of segment of samples temperature of C, methane partial pressure of kpa and residence time of s. The samples were cut in accordance with Fig. 2 for measurement. 2.2 Characterization of C/C composites One of the goals of this work is to study the infiltration process of preform. Therefore, the relative mass gain (RMG) of preform and the pore parameters of samples as a function of infiltration time were investigated, respectively. A 9310 mercury porosimeter made in US was used to determine the porosity and cumulative pore volumes of the as-received samples 1B and 2B at various infiltration time. RMG of preform and A s /V r were calculated in accordance with Eqs. (1) and (2), respectively: RMG = m m 0 m 0 (1) where m 0 is initial weight of preform and m is the weight of sample infiltrated. A s V r = Cumulative pore surface area per gram Cumulative pore volume per gram (2) The initial A s /V r of preform was calculated by Eq. (3): [ As ] = 2 1 P 0 1 (3) V r P 0 r 0 where P 0 is the porosity of preform and r 0 is the initial radius of fibers, which was 4 µm in our experiment. Fig. 4 The open porosity as a function of the infiltration time The texture of the as-received samples 1A and 2C at different infiltration time was observed under a Leica DLM polarized light microscope to study the mechanisms of abrupt transition texture of carbon. 3. Results and Discussion 3.1 Study of infiltration process Figure 3 shows RMG of the preform vs. the infiltration time, from which RMG of the preform increases with the prolonging of the infiltration time. Additionally, the curve can be roughly divided into two stages. In the first 20 h, it shows a similar linearity. After 20 h, the increment of RMG reduces gradually. Figure 4 shows the open porosity as a function of the infiltration time. It can be seen that the porosity of the samples is also reduced with the prolonging of the infiltration time. However, the porosity in the initial stage of densification decreases rapidly while that decreases slowly in the final stage, which conforms to trend of RMG of the preform. The porosity of the sample 1B is slightly lower than that of the sample 2B, which sufficiently proves that there exists weak diffusion limited in the improved ICVI techniques. The correlation between the accumulated pore volumes and pore radius distribution of the samples 1B and 2B is shown in Fig. 5. As the infiltration time increases from 5 to 125 h, the accumulated pore volumes of the samples 1B and 2B both decrease gradually and their difference becomes smaller and smaller. In the end of infiltration, the accumulated pore

3 J. Mater. Sci. Technol., Vol.25 No.1, Cumulative pore volum / cm 3 g -1 Cumulative pore volume / cm 3 g -1 Cumulative pore volume/cm 3 g (a) (b) (c) Pore radius / m 1B 2B Pore radius / m 1B 2B Pore radius / m 1B 2B Fig. 5 Cumulative pore volumes as a function of the pore radius of perform infiltrated. (a) 5 h, (b) 20 h, (c) 125 h volume of sample 2B is still higher than that of sample 1B (Fig. 5(c)). The relationship between the bulk density of the samples and the infiltration time is shown in Fig. 6, and the bulk density distribution as a function of the distance from the center of preform is shown in Fig. 7. In the initial stage of densification, the bulk density increases with the infiltration time, and the increasing rate of bulk density gradually reduced with the prolongation of time. After 100 h, no apparent changes occur. According to Fig. 7, there is nearly no difference in density between the inner region and the outer one in the initial stage of densification. However, with the proceeding of densification, the difference in bulk density gradually increases, though the final bulk density difference of the samples between the inner region and outer one is only around 0.05 g/cm 3. The CVI technique of C/C composites is extremely complicated. There exist the gas-phase reactions (homogeneous reactions), gas-solid phase reactions (heterogeneous reactions) and the diffusion of tha gas as well as their competition [19,20]. If the Bulk density / (g cm -3 ) Fig. 6 Bulk density as a function of infiltration time Bulk density / (g cm) h 10 h 50 h 75 h 100 h 125 h Distance from the center of the sample / mm Fig. 7 Bulk density as a function of the distance from the center of the samples infiltrated at different infiltration time gas-phase reaction is dominant, the diffusion limitation will appear, which will lead to a long densification period. This disadvantage exists in traditional ICVI techniques. If the gas-solid reaction is dominant, the infiltration rate is high. In this study, an improved ICVI technique was adopted to infiltrate the 2D needle-punched fiber felt [13]. By adjusting the gas flow volume, the shorter residence time of the gas in the reaction zone was obtained to control the pyrolysis reaction of precursor outside the preform. As a result, the densification period is much shorter than that of traditional ICVI techniques. In the initial stage of densification, RMG of the preform and the bulk density are in proportional to the infiltration time owing to the lower diffusion resistance of the flowing gases and the larger specific surface area of the preform. With the proceeding of densification, the volume of the porosity becomes smaller gradually as shown in Fig. 5, which results in the diffusion limitation due to the narrower tunnel of diffusion. Therefore, the increasing rates of RMG of the preform and the bulk density are both declined gradually. In the final stage of densification, the gas diffusion tunnel becomes far smaller and the amount of gas diffused into pores gets less and less so that the increment of RMG of the preform and bulk density become much smaller. At this time, the crust of pyrocarbon will be formed on the surface of the perform, resulting in the further increasing of density difference between the inner region and the outer one, as shown in Fig. 7. Under such a condition, the bulk density of the sample in the inner region cannot be enhanced obviously even if the infiltration time prolongs continuously.

4 112 J. Mater. Sci. Technol., Vol.25 No.1, 2009 Fig. 8 The polarized light microscopy of resultant samples 1A. The infiltration time of 5 h (a), 20 h (b), 75 h (c) and 125 h (d) Fig. 9 The polarized light microscopy of resultant samples 2C. The infiltration time of 5h (a), 20 h (b), 75 h (c) and 125 h (d) 3.2 Texture transition To control the texture of C/C composites is as important as the rapid and uniform densification because ideal microstructure endows the composites with good properties. Figure 8 shows the texture of the sample 1A after different densification time. In the initial densification (0 5 h), a layer of lowtextured (LT) pyrocarbon was infiltrated on the fiber surface as shown in Fig. 8(a), in which no optical activities could be found under a polarized light microscope. The color of the matrix is almost the same as that of the fiber. When the infiltration time reaches 20 h, a layer of high-textured (HT) pyrocarbon as shown in Fig. 8(b) was formed that possessed high reflectivity and the irregular extinction cross under the polarization. Meanwhile, HT became thicker as the densification time proceeds. The pores had been filled by HT when the infiltration time was 75 h as shown in Fig. 8(c). By the end of densification, a layer of LT had been produced on the HT surface among fiber bundles as shown in Fig. 8(d). The pyrocarbon textures of the sample 2C are similar to those of the sample 1A after same infiltration time (Fig. 9). In experiments, the infiltration temperature, the partial pressure of the precursor outside the preform and the residence time of the gas remained constant. Thus, the variation of the texture is only attributed to the

5 J. Mater. Sci. Technol., Vol.25 No.1, A s /V r / 10 3 mm Outside Inside Fig. 10 The surface area/volume ratio as a function of the infiltration time determined for pore entrance diameter larger than µm variation of A s /V r ratios and partial pressure of precursor in pores. Consequently, the variation of A s /V r ratio as a function of densification time was investigated as shown in Fig. 10. The A s /V r ratio first increases apparently and then slightly decreases and increases again with the prolonging of the densification time. At the initial stage of densification, most fibers are not joint with one another, so the total surface area of the pores increases and the volume decreases with the thickening of pyrocarbon on the fiber surface, leading to the increase in A s /V r ratio obviously. As the densification time is about 20 h, fibers inside the fiber bundles are connected by pyrocarbon, resulting in the reduction of the A s /V r ratio. After h, the pyrocarbon infiltration mainly takes place in larger pores among fiber bundles. Under such a condition, pores can be approximately regarded as hollow spheres. Then A s /V r is equal to 16/3R (R is the radius of the sphere). Therefore, with the densification proceeding, the radius of the spheres becomes smaller gradually, resulting in the increase in A s /V r ratio. The A s /V r ratio controls the competition between the gas-phase pyrolysis reactions and gas-solid heterogeneous reactions [20]. The higher A s /V r ratio means the smaller pore volume and the larger surface area, which is beneficial to the gas-solid heterogeneous reactions. On the contrary, the smaller A s /V r ratio signifies the smaller surface area and the larger pore volume, which is beneficial to the gas-phase reactions. According to the Particle-filler mode and G-T model [21,22], when the proportions of aromatic molecule particle (such as benzene, anthracene, naphthalene and other aromatic molecules) and small linear molecule filler (acetylene as the major component) in a gas mixture reach an optimal value scope, HT pyrocarbon can be formed. Otherwise, the lower-textured (LT or MT) pyrocarbon will be formed for the excess of the amount of aromatic molecule or small linear molecule. The transition texture can be explained by combining the Particle-filler mode with A s /V r ratio variety. In the initial stage of densification, a layer of LT is firstly infiltrated on the fiber surface. On the one hand, the pore radius is bigger, so the resistance of gas flow is lower, leading to the higher gas partial pressure in the pores. On the other hand, the A s /V r ratio of preform is lower. The higher gas partial pressure and the lower A s /V r ratio are both in favor of the sufficient pyrolysis reaction in the gas phase. Thus, the excessive aromatic molecules are produced. After 20 h, the A s /V r ratio increases gradually and partial pressure of precursor in pore reduces gradually. The pyrolysis reaction of precusor in pore is restricted, which leads to the reduction of amount of aromatic molecules. At this time, the ratio of the larger aromatic molecules to the smaller linear molecules in the gases is in an optimum scope such that the HT is formed on the surface of LT as shown in Fig. 8(b) and (c). In the later densification period, the pore radius becomes smaller and smaller and the pores inside the fiber bundles are nearly full of pyrocarbon. At this time, A s /V r ratio is very high and partial pressure of precursor in the pores become very low, which is not in favor of the gas-phase reaction. The amount of gases that diffuse into the pores is much small and the surface area of the pores is still large. Therefore, the gas-phase pyrolysis reaction of precusor in pores cannot take place sufficiently, resulting in the excess of small linear molecules, so LT is formed on the surface of HT again. 4. Conclusions (1) The increment of RMG of preform depends on the variation of A s /V r. In the initial stage of densification of C/C composites, RMG of the preform increases linearly with the densification time. As the densification proceeds, the increment of RMG of the preform becomes slower and slower. (2) The porosity and accumulated pore volume gradually reduces and the difference in accumulate pore volume between the interior and the exterior of the sample gradually decreases as the densification proceeds. (3) The A s /V r value first increases apparently and then decreases and increases again with the prolonging of the densification time. 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