APPROXIMATIONS FOR THE TEMPERATURE INTEGRAL Their underlying relationship

Transcription

1 Journal of Thermal Analysis and Calorimetry, Vol. 9 (08), APPROXIMATIONS FOR THE TEMPERATURE INTEGRAL Their underlying relationship H. X. Chen * and N. A. Liu ** State Key Laboratory of Fire Science, University of Science and Technology of China Hefei, Anhui 3006, P. R. China The temperature integral cannot be analytically integrated and many simple closed-form epressions have been proposed to use in the integral methods. This paper first reviews two types of simple approimation epressions for temperature integral in literature, i.e. the rational approimations and eponential approimations. Then the relationship of the two types of approimations is revealed by the aid of a new equation concerning the 1 st derivative of the temperature integral. It is found that the eponential approimations are essentially one kind of rational approimations with the form of h()=a+k That is, they share the same assumptions that the temperature integral h() can be approimated by A+k It is also found that only two of the three parameters in the general formula of eponential approimations are needed to be determined and the other one is a constant in theory. Though both types of the approimations have close relationship, the integral methods derived from the eponential approimations are recommended in kinetic analysis. Keywords: Approimation, temperature integral, thermal analysis, underlying relationship Introduction Thermal analysis techniques, such as thermogravimetry (TG) and differential scanning calorimetry (DSC), have been widely used to study the kinetics and mechanism of solid-state thermal decomposition process, generally carried out under a linear temperature program. The kinetic triplet (activation energy E, frequency factor A and kinetic model) can be derived from the eperimental data based on the kinetic equation of solid-state decomposition process as follows: d A ep( ERT / ) f( (1) dt where (0<<1) is the fractional conversion, (K s 1 ) the heating rate, E (kj mol 1 ) the activation energy, A (s 1 ) the pre-eponential factor, and R the gas constant. T (K) is the absolute temperature. The specific form of f() represents the hypothetical kinetic model of the reaction mechanism. The approaches to etract the kinetic triplet (E A f()) from the above epression may be generally classified as the differential methods and the integral methods. The main difference between the two classes of methods is that the differential methods refer to local data and offer the values of the kinetic parameters in the given point, whilst the integral ones refer to interval data and offer the values of the kinetic parameters averaged for the considered interval. For the integral methods, integrating Eq. (1) and substituting =E/RT for T gives: AE G ( ) R p ( ) where G( ( ) ) d f ( ), p ( ) e 0 d () Here p() is the well-known Arrhenius temperature integral. Although the integral methods are believed to be more reliable and accurate than the differential methods, the temperature integral has been a subject of much concern and controversy for a long time, since it cannot be analytically integrated. Many authors have proposed etensive approimations for the temperature integral p() with different mathematical compleities and numerical precisions. Flynn provided a review on the various approimate epressions for the temperature integral, in which the solutions of the temperature integral are classified into three categories, i.e. series solution, comple approimations and simple approimations. In fact, most of the comple and simple approimations can be derived from one-term, two-term or three-term * Author for correspondences: hchen@ustc.edu.cn ** liunai@ustc.edu.cn /$.00 Akadémiai Kiadó, Budapest, Hungary 08 Akadémiai Kiadó, Budapest Springer, Dordrecht, The Netherlands

2 CHEN, LIU truncations of different series solutions. Besides, some simple approimations are obtained through data-fitting process, and another kind of approimations are proposed through integration over small temperature intervals to enhance the accuracy. Recently, some new simple approimations with high precision are proposed. Though so many approimations for the temperature integral have appeared in the literature, it seems that there are very few papers considering the critical appraisal of the approimations and especially, the inherent relationship of the approimations. In this work, an equation concerning the 1 st order derivative of the temperature integral is proposed and then, the relationship of various approimations for the temperature integral is presented. It is shown that many approimations share the same assumption. Theoretical background A range of the approimations for the temperature integral p() have been suggested in literature, and here we will consider the best known and the most accurate approimations. Firstly we introduce another function, h(, to simplify the mathematical forms of some approimations. h() is defined as: h() =p() e or p ( ) e h ( ) (3) The values of p() andh() are calculated vs. by numerical integral and showed in Fig. 1. Compared with p(), h() varies slowly and has an asymptotic value of 1 as increases, and consequently it may be more easy to eplore or appraise the approimations for the temperature integral. Both p() and h() can be called the temperature integral. Fig. 1 Values of h()and p() in the domain of 1100 As pointed out in our previous paper [], the integral methods can be generally classified into two categories. The difference is that one type of integral methods uses the rational approimations for the temperature integral and the other uses the eponential approimations. The term of rational approimations was first proposed by Senum and Yang [10], who provided a series of such approimations. The fourth order approimation, which is believed to hold very high accuracy, is given by: h ( ) (4) The simplest one of rational approimations is Frank Kameneskii s approimation [4]: h ( )1 (5) and the classical one is Coats Redfern s approimation [3]: h ( ) 1 (6) There are many other forms of rational approimations [5 7, 14, 16, 19]. Recently, some new ones were proposed, for eample: h ( ) (Wanjun Yumen [13]) (7). h ( ) (Cai [1]) (8) It seems that eploring new approimations through data-fitting process or parameter optimization has become fashionable. The new approimations are often more accurate. However, it should be noted that only very simple approimations can be considered for use in thermal analysis [, 1]. In mathematical sense, reasonable approimations should be able to be justified by their accordance with the mathematical features of the temperature integral. For eample, the approimation is anticipated to approach unity as increases since the function of h() has an asymptotic value of 1. In this sense, Eq. (7) is somewhat of deviation. The term of eponential approimations refers to the approimations which contain eponential function, or equivalently logarithmic function, as follows []: lnhaln+b+c or lnpa'ln+b'+c' (9) where a, b, c, a', b', c' are the parameters and a, b are not both zero (otherwise it will become a rational 574 J. Therm. Anal. Cal., 9, 08

3 APPROXIMATIONS FOR THE TEMPERATURE INTEGRAL Table 1 Typical values of the parameters appeared in the eponential approimation as p()=ep( A+B)/ k Source A k B No. Doyle [] Starink [3] Starink [3] Madhusudanan et al. [15] Madhusudanan et al. [8] Madhusudanan et al. [8] Tang et al. [11] approimation, for eample, Frank Kameneskii s approimation). The most famous eponential approimation was suggested by Doyle []: p ( ) ep( ) (10) Another widely-used approimation of this kind was first proposed by Madhusudanan et al. [15], for which the approimate formula of ln[p()] is ln[ p ( )] ln (11) Madhusudanan et al. [15] also proposed the general formula of eponential approimations as a1 b a b1 p ( )e e. Starink [3] provided another general formula as p()=ep( A+B)/ k recently. It is obvious that the two formulae are identical in mathematics. Table 1 lists some typical values of the parameters appeared in Starink s general formula of eponential approimations. Relationship of the eponential and the rational approimations The eponential and rational approimations are deduced from different mathematical approaches and both are widely used in thermal analysis as two types of integral methods []. It seems that no discussion concerning the relationship of the two types of approimations appeared in literature. Here we will consider how the two types of approimations are related to each other. The general formula of eponential approimations p()=ep( A+B)/ k can be arranged into the form of Eq. (9): ln[h()]=( k)ln+(1 A)+B. The differential form of this equation is: h' ( ) k ( 1 A) (1) h ( ) By differentiating the definition equation of h(), h()e =p(), we can obtain the 1 st order derivative of the function h(): h ' ( ) 1 h ( ) 1 (13) This equation seems to appear firstly in our previous paper []. It has many applications for the research of temperature integral, for eample, higher order derivative can be deduced and then a series of new approimations for the temperature integral can be obtained [19]. Combining the Eqs (1) and (13), one can obtain: h ( ) (14) Ak It is very interesting that Eq. (14) is just one kind of the rational approimations. That is to say, the eponential approimations in essence belong to the rational approimations, and are very simple rational approimations. They share the same assumption that the temperature integral h() can be approimated by /(A+k). If A=1, Eq. (14) becomes ordinary rational approimations, for eample, Gorbachev s approimation [5]. It is surprising that the rational approimation with the form of Eq. (14) and A1, i.e. Eq. (7), was proposed just a few years ago. And in the above part, it is pointed out that Eq. (7) is somewhat of deviation from mathematical features of h(). Maybe this consideration delays the discovery of more rational approimations with the form of Eq. (14). Two parameters of the eponential approimation p()=ep( A+B)/ k, A and k, appear in Eq. (14). Where is B? It can be deduced that B is an integral constant. Integrating Eq. (1) in the range [ 0, ] will produce: with ln[ h ( )] ( k) ln( 1 A ) B (15) Bln[ h( 0)] ( k)ln0 ( 1 A) 0 (16) From this equation, it is obvious that B is a constant and can be calculated directly, however, many papers have regarded it as a variable which needs to be determined. In fact, the values of B calculated from Eq. (16) will vary a little with 0 (see J. Therm. Anal. Cal., 9,

4 CHEN, LIU below), which roots in the assumption that the temperature integral can be approimated by p()=ep( A+B)/ k. Thus the rationality of the eponential approimations can be assessed through the deviation degree of B from its average value. In the following, we will analyze all the three parameters (A k B) of the eponential approimations presented in Table 1 in detail. No. 1: Doyle s approimation In Doyle s approimation (Eq. (10)), k=0. So Eq. (14) can be converted into: h ( ) 1 (17) A i.e. the underlying assumption of Doyle s approimation is that the function h() can be regarded as a constant. The parameter A has a physical meaning that it is the reciprocal of averaged value (represented by h() in the following) of h(). So it can be obtained theoretically other than through Doyle s approaches. In the range of [, ] which is the valid domain of Doyle s approimation, h() can be calculated as: h ( ) h ( ) d/ ldp ( ) e d/ 40 (18) By combining the asymptotic epansion of p(), Eq. (18) becomes: ( j )! h ( ) j e ( 1) 1 1 e d/ 40 j j= ln j= 1 j ( 1) j ( j+ 1)! 1 j / (19) Thus from Eq. (17), A equals 1.053, which is very close to in Doyle s approimation. As for the parameter B, it can be calculated from Eq. (16). Figure gives the theoretical value of B when 0 is sampled from the range of [, ]. Here h() is approimated by Eq. (4) and A= It can be seen that B varies with the value of 0 and differs from which appeared in Doyle s approimation. This is because Doyle s assumption (Eq. (17)) is too simple and deviates much from the true values. Therefore this approimation should be used carefully. No. : Starink s approimation According to Eq. (14), Starink s approimation is equal to: h ( ) () 195. It can be regarded as an improvement of Gorbachev s approimation [5], where h()=/(+). Because Eq. () is also very simple, it can be deduced that the values of B from Eq. (16) will differ from 0.35 in Starink s approimation, as Fig. 3 shows. Fig. 3 Comparison of the values of B calculated from Eq. (16) with the value from Table 1 for Starink s approimation (No. ) No. 3 7: M-approimations Fig. Comparison of the values of B calculated from Eq. (16) with the value from Table 1 for Doyle s approimation The approimations represented by No. 3 7 (named as M-approiamtions for convenience) in Table 1 have some common features. Madhusudanan s approimations (No. 4 6) are derived from the twoor three-term truncations of MKN epansion of p() [15]. No. 3 and 7 can be regarded as the improved forms of Madhusudanan s approimations. Especially, No. 7 used two-step linearly fitting process to obtain more accurate (A k B) values and the corresponding integral methods are more reliable. 576 J. Therm. Anal. Cal., 9, 08

5 APPROXIMATIONS FOR THE TEMPERATURE INTEGRAL Here we can point out that only the first-step linearly fitting process (to determine A and k) in their paper is necessary and the second-step (to determine B) can be omitted because B is an integral constant. M-approimations are identical to Eq. (14) with more accurate values of (A k). Up to now, the most accurate values appear in Eq. (7) with A= and k= Then the value of B can be determined from Eq. (16). Obviously, the values of (A k) depend on the range of and the accuracy can be enhanced by reasonable manipulation of Eq. (14). For eample, Eq. (14) can be linearized as: y=a+k, y (1) h ( ) In the range of [15, ] (in which the overwhelming majority of reactions occur [3]), the fitted line will produce the parameters with A= and Fig. 4 The linear relationship of y=/h() with in the range of [15, ] Fig. 5 Comparison of the values of B calculated from Eq. (16) with the value from Table 1 for M-approimation (No. 3 7) k= (Fig. 4, data points are sampled from [15, ] with the interval of 0.01). When (A k) are set, the value of B can be calculated by Eq. (16). Figure 5 presents the theoretical B values compared with the values from Table 1. It can be seen that Starink s and Tang s approimations hold higher precision than others and thus they are recommended in thermal analysis. Conclusions The temperature integral has played a somewhat enigmatic role in the development of thermal analysis reaction kinetics [17]. Many of the problems have resulted from the inability to accurately approimate the temperature integral by a simple closed-form epression which is suitable for use in the integral methods. So various approimations for the temperature integral have appeared in literature. As two main types of approimations, the rational and eponential approimations have been proposed separately and developed into two types of integral methods. In this paper, the relationship of the rational and eponential approimations is revealed by the aid of a new equation concerning the 1 st derivative of the temperature integral. It is found that the eponential approimations are essentially one kind of the rational approimations with the form of h()=/(a+k). That is, they share the same assumptions that the temperature integral h() can be approimated by /(A+k). It is also found that only two of the three parameters in the general formula of eponential approimations are needed to be determined and the other one is a constant in theory. Though the eponential approimations belong to the rational approimations, their corresponding integral methods use them in different ways. For eample, the rational approimation Eq. (7) is used as: G( ) ln T AR ln ( E RT) E RT () The integral method still needs to assume that AR ln ( E RT) is nearly a constant for T and the plot of lng()/t ~1/T would result in a straight line for the correct reaction model. While the eponential approimation No. 7 [11] is used as: J. Therm. Anal. Cal., 9,

6 CHEN, LIU G( ) ln. T AE ln ln E R (3) E RT The plot of lng()/t ~1/T will result in a straight line for the correct reaction model. This integral method adopts no assumptions other than the approimation for the temperature integral and will be more accurate in the calculation of kinetic parameters []. Therefore, the integral methods, which are derived from the eponential approimations, are recommended to be a prior choose in kinetic analysis, though the eponential approimations in essence are one kind of the rational approimations. Acknowledgements This work was sponsored by China Postdoctoral Science Foundation, National Natural Science Foundation of China under Grants , and the Program for New Century Ecellent Talents in University. References 1 C. Popescu and E. Segal, International J. Chem. Kinetics, 30 (1998) 313. J. H. Flynn and L. A. Wall, J. Res. Nat. Bur. Stds., 70A (1966) A. W. Coats and J. P. Redfern, Nature, 1 (1964) D. A. Frank-Kamenenskii, Princeton University, Princeton V. M. Gorbachev, J. Thermal Anal., 8 (1975) T. V. Lee and S. R. Beck, AIChE J., 30 (1984) C. H. Li, AIChE J., 31 (1985) P. M. Madhusudanan, K. Krishnan and K. N. Ninan, Thermochim. Acta, 1 (1993) 13. 9J.esták, V. Satava and W. W. Wendlandt, Thermochim. Acta, 7 (1973) J. I. Senum and R. T. Yang, J. Thermal Anal., 11 (1977) W. J. Tang, Y. W. Liu, H. Zhang and C. X. Wang, Thermochim. Acta, 408 (03) J. M. Cai, F. S. Yao, W. M. Yi and F. He, AIChE J., 5 (06) T. Wanjun, L. Yuwen, Z. Hen, W. Zhiyong and W. Cunin, J. Therm. Anal. Cal., 74 (03) Q. Y. Ran and S. Ye, J. Thermal Anal., 44 (1995) P. M. Madhusudanan, K. Krishnan and K. N. Ninan, Thermochim. Acta, 97 (1986) R. K. Agrawal, AIChE J., 33 (1987) J. H. Flynn, Thermochim. Acta, 300 (1997) E. Urbanovici and E. Segal, Thermochim. Acta, 3 (199) H. X. Chen and N. Liu, AIChE J., 5 (06) N. Liu, H. Chen, L. Shu and M. Statheropoulos, J. Therm. Anal. Cal., 81 (05) A. Ortega, L. A. Perez Maqueda and J. M. Criado, Thermochim. Acta, 83 (1996) 9. C. D. Doyle, J. Appl. Polym. Sci., 5 (1961) M. J. Starink, Thermochim. Acta, 404 (03) 163. Received: January 5, 07 Accepted: April 17, 07 OnlineFirst: January 6, 08 DOI: /s J. Therm. Anal. Cal., 9, 08