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Article

Some Aspects of Extended Kinetic Equation

Department of Basic Sciences, Amal Jyothi College of Engineering, Koovapally P.O., Kanjirapally, Kerala 686518, India
Axioms 2015, 4(3), 412-422; https://doi.org/10.3390/axioms4030412
Submission received: 20 May 2015 / Revised: 27 August 2015 / Accepted: 31 August 2015 / Published: 18 September 2015

Abstract

:
Motivated by the pathway model of Mathai introduced in 2005 [Linear Algebra and Its Applications, 396, 317–328] we extend the standard kinetic equations. Connection of the extended kinetic equation with fractional calculus operator is established. The solution of the general form of the fractional kinetic equation is obtained through Laplace transform. The results for the standard kinetic equation are obtained as the limiting case.
MSC Classification:
35K57; 26A33; 44A35; 33C60; 33E12

1. Introduction

The chemical evolution of a star like sun could be effectively explained by kinetic equations. The kinetic equations explain the rate of change of chemical composition of a star in terms of the thermonuclear reaction rates for destruction and production of the species involved. An arbitrary reaction is characterized by the rate of change d N d t of a time dependent quantity N ( t ) between the destruction rate d and production rate p. Here the destruction or production at time t depends not only on N ( t ) but also on the past history N ( τ ) , τ < t of the variable N. This may be formally represented by following [1,2]
d N ( t ) d t = d ( N t ) + p ( N t )
where N t denotes the function defined by N t ( t * ) = N ( t t * ) , t * > 0 . It should be noted that d and p are functionals and Equation (1) represents a functional-differential equation. If we consider a simplified form of Equation (1) we could consider the decay rate of a radio-active substance which is given by a homogeneous differential equation
d N d t = λ N
where N is the number density of the radio-active substance and λ is the decay constant. The solution of this differential equation with initial condition N = N 0 at t = 0 is
N ( t ) = N 0 e λ t
If we consider a more general form of the differential Equation (2) for the decay rate of a radio-active substance as
d N d t = λ N α
we have the solution of the form
N α ( t ) = N 0 [ 1 + a ( α 1 ) t ] 1 α 1
where a is a constant. One may get the solution in Equation (3) from Equation (5) as α 1 . These types of problems arise in many experimental situations where one needs to switch from one family of functions to another family. In 2005, Mathai [3,4] introduced the pathway model by which one can switch among three different families of functions, say, type-1 beta families, type-2 beta families and gamma families. We get three different functional forms by varying the pathway parameter α. The pathway model in the real scalar case is defined as
f ( x ) = c 1 | x | γ [ 1 a ( 1 α ) | x | δ ] η 1 α , 1 a ( 1 α ) | x | δ > 0 , α < 1 c 2 | x | γ [ 1 + a ( α 1 ) | x | δ ] η α 1 , < x < , α > 1 c 3 | x | γ e a η | x | δ , < x < , α 1
where a > 0 , δ > 0 , γ > 0 , η > 0 . c 1 , c 2 and c 3 are the normalizing constants when we consider the functions as statistical densities. The three different functional forms are respectively generalized type-1 beta, generalized type-2 beta and generalized gamma forms. By writing 1 α = ( α 1 ) , the generalized type-2 beta form can be obtained from generalized type-1 beta form. Both generalized type-1 beta form and generalized type-2 beta form reduce to generalized gamma form as α 1 .
Due to this switching property, the pathway model has been widely used in many areas. In this paper, we use the pathway model to extend kinetic equations. The present paper is organized as follows: In the next section we discuss the extended kinetic equation and its solution with a brief description of the extended reaction rate probability integral. Connection of the extended kinetic equation with fractional calculus is examined in Section 3. In Section 4 we try to solve fractional kinetic equations and their various generalizations. Concluding remarks are given in Section 5.

2. Extended Kinetic Equations

The following discussion is based on [1,2]. If we consider a production and destruction of nuclei in the proton-proton chain reaction, we can describe it by the equation
d N i d t = j N i N j σ v i j + k , l i N k N l σ v k l
where N i is the number density of the species i over time. Here the summation is taken over all reactions, productions or destructions of the species i. The number density N i of the species i can be expressed by the relation N i = ρ N A X i A i where ρ is the mass density, X i is the mass abundance, N A is the Avogadro number and A i is the mass of species i in mass units. The mean life time τ j ( i ) of species i for destruction by species j is given by the relation [2]
λ j ( i ) = 1 τ j ( i ) = N j σ v i j = ρ N A X j A j σ v i j
where λ j ( i ) is the decay rate of i for interaction with j. σ v i j denotes the reaction probability for an interaction involving species i and j defined as
σ v i j = 2 μ 0 E 1 2 f ( E ) σ ( E ) d E
where μ is the reduced mass of the particles given by μ = m 1 m 2 m 1 + m 2 , E = μ v 2 2 is the kinetic energy of the particles in the center of mass system. Consider the cross section σ ( E ) for low-energy non-resonant reactions given by
σ ( E ) = ν = 0 2 S ( ν ) ( 0 ) ν ! E ν 1 e 2 π μ 2 1 2 Z i Z j e 2 E 1 2 E B 1
where Z i and Z j are the atomic numbers of the nuclei i and j, e is the quantum of electric charge, is the Planck’s quantum of action, B the nuclear barrier height, S ( E ) is the cross-section factor which is a slowly varying function of energy over a limited energy range and which can be characterized depending on the nuclear reaction. The density function of the relative velocities of the nuclei for a non-degenerate and non-relativistic gas is assumed to be Maxwell-Boltzmann given as
f M B D ( E ) d E = 2 π 1 π k T 3 2 e E k T E d E
By substituting Equation (11) and Equation (10) in Equation (9) the reaction probability σ v i j is obtained as
σ v i j = 8 π μ 1 2 1 k T 3 2 ν = 0 2 S ( ν ) ( 0 ) ν ! 0 E ν e E k T 2 π μ 2 1 2 Z i Z j e 2 E 1 2 d E
If a deviation from the thermodynamic equilibrium with regard to their velocities is considered then it results in a deviation from the Maxwell-Boltzmann velocity. In this context, we consider a more general density function than Maxwell-Boltzmann density function by using the pathway model defined in Equation (6). The pathway energy density function has the form
f P D ( E ) d E = 2 π ( α 1 ) 3 2 ( π k T ) 3 2 Γ 1 α 1 Γ 1 α 1 3 2 E 1 + ( α 1 ) E k T 1 α 1 d E
for α > 1 , 1 α 1 3 2 > 0 . Replacing the Maxwell-Boltzmann density Function Equation (11) by the pathway energy density Equation (13), we get the extended thermonuclear reaction probability integral in the form
σ v i j = 8 π μ 1 2 α 1 k T 3 2 Γ 1 α 1 Γ 1 α 1 3 2 ν = 0 2 S ( ν ) ( 0 ) ν !
× 0 E ν 1 + ( α 1 ) E k T 1 α 1 exp 2 π μ 2 1 2 Z i Z j e 2 E 1 2 d E
Putting y = E k T and x = 2 π μ 2 k T 1 2 Z i Z j e 2 we get
σ v i j = 8 π μ 1 2 ( α 1 ) 3 2 Γ 1 α 1 Γ 1 α 1 3 2 ν = 0 2 1 k T ν + 1 2 S ( ν ) ( 0 ) ν ! I 1 α ( ν , 1 , x , 1 2 )
where
I 1 α ( ν , 1 , x , 1 2 ) = 0 y ν [ 1 + ( α 1 ) y ] 1 α 1 e x y 1 2 d y
Following [5], by taking the Mellin transform of Equation (16) and simplifying, we get
M I 1 α ( s ) = Γ ( s ) Γ ( ν + 1 + s 2 ) Γ 1 α 1 ν 1 s 2 ( α 1 ) ν + 1 + s 2 Γ 1 α 1
where ( s ) > 0 , ( ν + 1 + s 2 ) > 0 , 1 α 1 ν 1 s 2 > 0 . By taking the inverse Mellin transform we get,
I 1 α ( ν , 1 , x , 1 2 ) = 1 ( α 1 ) ν + 1 Γ 1 α 1 1 2 π i L Γ ( s ) Γ ( ν + 1 + s 2 )
× Γ 1 α 1 ν 1 s 2 [ x ( α 1 ) 1 2 ] s d s
where L is a suitable contour which separates the poles of Γ ( s ) and Γ ( ν + 1 + s 2 ) from the poles of Γ 1 α 1 ν 1 s 2 . Putting s = 2 s and using Legendre’s duplication formula [6]
Γ ( 2 z ) = π 1 2 2 2 z 1 Γ ( z ) Γ z + 1 2 , z C
we get
I 1 α ( ν , 1 , x , 1 2 ) = π 1 2 ( α 1 ) ν + 1 Γ 1 α 1 1 2 π i L Γ ( s ) Γ ( 1 2 + s ) Γ ( ν + 1 + s )
× Γ 1 α 1 ν 1 s ( α 1 ) x 2 4 s d s
= π 1 2 ( α 1 ) ν + 1 Γ 1 α 1 G 1 , 3 3 , 1 ( α 1 ) x 2 4 | 0 , 1 2 , ν + 1 2 1 α 1 + ν
where G 1 , 3 3 , 1 ( . ) is the G-function originally introduced by C.S. Meijer in 1936, see [5,7,8]. The G 1 , 3 3 , 1 ( . ) used in Equation (21) converges for all ( α 1 ) x 2 4 , x 0 . The contour line L appearing in the integral in Equation (20) is c i to c + i for 0 < c < 1 α 1 ν 1 so that all the poles of Γ ( s ) , Γ ( 1 2 + s ) and Γ ( ν + 1 + s ) lie to the left and all the poles of Γ 1 α 1 ν 1 s lie to the right. G 1 , 3 3 , 1 ( . ) is evaluated as the sum of the residues at the poles of Γ ( s ) , Γ ( 1 2 + s ) and Γ ( ν + 1 + s ) .
In most of the cases the nuclear factor S ( ν ) ( 0 ) used in Equation (15) is approximately constant across the fusion window. Hence taking S ( ν ) ( 0 ) = 0 for ν = 1 and ν = 2 and taking S 0 ( 0 ) = S ( 0 ) we get
σ v i j = 8 ( α 1 ) μ k T 1 2 1 π Γ 1 α 1 3 2 S ( 0 ) G 1 , 3 3 , 1 ( α 1 ) x 2 4 | 0 , 1 2 , 1 2 1 α 1
The following derivations are adapted from [9]. From the Mellin-Barnes representation of the G-function, G 1 , 3 3 , 1 ( ( α 1 ) x 2 4 ) appearing in Equation (20) with ν = 0 , the poles of Γ ( s ) are s = 0 , 1 , 2 , ; the poles of Γ 1 2 + s are s = 1 2 , 3 2 , 5 2 , ; and the poles of Γ ( 1 + s ) are s = 1 , 2 , 3 , . Here the poles of Γ ( s ) and Γ ( 1 + s ) will coincide at all points except at s = 0 and hence the pole s = 0 is a pole of order 1, s = 1 2 , 3 2 , 5 2 , are each of order 1 and s = 1 , 2 , 3 , are each of order 2. The sum of residues corresponding to the pole s = 0 is given by
R 1 = π Γ 1 α 1 1
The sum of the residues corresponding to the poles s = 1 2 , 3 2 , 5 2 , is
R 2 = r = 0 ( 1 ) r r ! Γ ( 1 2 r ) Γ ( 1 2 r ) Γ ( 1 α 1 1 2 + r ) ( α 1 ) x 2 4 1 2 + r
= 2 π Γ 1 α 1 1 2 ( α 1 ) x 2 4 1 2 1 F 2 1 α 1 1 2 ; 3 2 , 1 2 ; ( α 1 ) x 2 4
where 1 F 2 is the hypergeometric function defined by
1 F 2 ( a ; b , c ; x ) = r = 0 ( a ) r ( b ) r ( c ) r x r r !
where
( a ) r = a ( a + 1 ) ( a + r 1 ) if r 1 , a 0 1 if r = 0
The sum of the residues corresponding to poles s = 1 , 2 , 3 , . of order 2 can be obtained as follows:
R 3 = r = 0 lim s 1 r s [ ( s + 1 + r ) 2 Γ ( 1 + s ) Γ ( s ) Γ 1 2 + s × Γ 1 α 1 1 s ( α 1 ) x 2 4 s ] = r = 0 lim s 1 r s Γ 2 ( 2 + s + r ) Γ 1 2 + s Γ 1 α 1 1 s ( s + r ) 2 ( s + r 1 ) 2 ( s + 1 ) 2 s ( α 1 ) x 2 4 s
= r = 0 lim s 1 r s Φ ( s )
where
Φ ( s ) = Γ 2 ( 2 + s + r ) Γ 1 2 + s Γ 1 α 1 1 s ( s + r ) 2 ( s + r 1 ) 2 ( s + 1 ) 2 s ( α 1 ) x 2 4 s
We have
s Φ ( s ) = Φ ( s ) s [ ln ( Φ ( s ) ]
ln Φ ( s ) = 2 ln Γ ( 2 + s + r ) + ln Γ 1 2 + s + ln Γ 1 α 1 1 s s ln ( α 1 ) x 2 4 2 ln ( s + r ) 2 ln ( s + 1 ) ln ( s ) s [ ln ( Φ ( s ) ] = 2 Ψ ( 2 + s + r ) + Ψ 1 2 + s + Ψ 1 α 1 1 s ln ( α 1 ) x 2 4 2 s + r 2 s + r 1 2 s + 1 1 s
lim s 1 r { s ln [ Φ ( s ) ] } = Ψ 1 2 r + Ψ 1 α 1 + r + Ψ ( 1 + r )
+ Ψ ( 2 + r ) ln ( α 1 ) x 2 4
where Ψ ( z ) is a Psi function or digamma function (see Mathai [5]) and Ψ ( 1 ) = γ , γ = 0 . 5772156649 is Euler’s constant. Now
lim s 1 r Φ ( s ) = ( 1 ) 1 + r 2 π Γ 1 α 1 + r 3 2 r r ! ( 1 + r ) ! ( α 1 ) x 2 4 1 + r
Then by using Equation (25)–Equation (27) we get,
R 3 = r = 0 ( 1 ) 1 + r 2 π Γ 1 α 1 + r 3 2 r r ! ( 1 + r ) ! ( α 1 ) x 2 4 1 + r
× Ψ 1 2 r + Ψ 1 α 1 + r + Ψ ( 1 + r ) + Ψ ( 2 + r ) ln ( α 1 ) x 2 4
= 2 π ( α 1 ) x 2 4 r = 0 ( α 1 ) x 2 4 r A r ln ( α 1 ) x 2 4 B r
where
A r = Ψ 1 2 r + Ψ 1 α 1 + r + Ψ ( 1 + r ) + Ψ ( 2 + r )
and
B r = ( 1 ) r Γ 1 α 1 + r 3 2 r r ! ( 1 + r ) !
Thus the series representation for the reaction probability is
σ v i j = 8 ( α 1 ) μ k T 1 2 1 Γ 1 α 1 3 2 S ( 0 ) { 1 π Γ 1 α 1 1
2 Γ 1 α 1 1 2 ( α 1 ) x 2 4 1 2 1 F 2 1 α 1 1 2 ; 3 2 , 1 2 ; ( α 1 ) x 2 4
+ 2 ( α 1 ) x 2 4 π r = 0 ( α 1 ) x 2 4 r A r ln ( α 1 ) x 2 4 B r }
where A r and B r are as defined in Equations (29) and (30). For detailed theory of extended reaction rates and its series representations see Haubold and Kumar [10,11], Kumar and Haubold [12].
The following discussion is adapted from [1]. The solution of the differential Equation (4) with initial condition N i ( t ) = 1 when t = 0 is
N i α ( t ) d t = [ 1 + ( α 1 ) c i t ] 1 α 1 d t
When c i in Equation (32) is a constant, the total number of reactions in the time interval 0 t t 0 is obtained as
0 t 0 N i α ( t ) d t = 0 t 0 [ 1 + ( α 1 ) c i t ] 1 α 1 d t = 1 c i ( 2 α ) [ 1 + ( α 1 ) c i t 0 ] 2 α α 1 1
Now [ 1 + ( α 1 ) c i t 0 ] 2 α α 1 1 is the probability that the lifetime of species i is t 0 when t follows a distribution with density function
f ( t ) = c i ( 2 α ) [ 1 + ( α 1 ) c i t ] 1 α 1 , 0 t < , c i > 0 , 1 < α < 2
or we have
N i ( t ) = f ( t ) c i ( 2 α )
Equation (34) is the Tsallis statistics for α > 1 , see [13,14] which can also be seen as a particular case of the pathway model Equation (6) for α > 1 . If c i in Equation (32) is a function of time, say c i ( t ) , then it should be replaced by c i ( t ) d t . When c i = c i ( t ) = d i t where d i > 0 is independent of t, then in this case c i ( t ) d t = d i t 2 2 , then
N i ( t ) = Γ 1 α 1 1 2 Γ 1 α 1 π 2 d i ( α 1 ) 1 2 g ( t )
where
g ( t ) = Γ 1 α 1 Γ 1 α 1 1 2 2 d i ( α 1 ) π 1 2 [ 1 + ( α 1 ) d i t 2 2 ] 1 α 1 , 0 t < , d i > 0 , 1 < α < 2
The density in Equation (34) is the lifetime density of the destruction of the species i, with the expected mean value
E ( t ) = 1 c i ( 3 2 α )
where E ( · ) is the expected value of ( · ) . The mean value of the lifetime density function given in Equation (37) is
E ( t ) = Γ 1 α 1 Γ 1 α 1 1 2 2 ( α 1 ) π d i 1 2 1 2 α
Now as α 1 we get the expected mean lifetime
E ( t ) = 2 π d i 1 2
of the lifetime density function
g * ( t ) = 2 d i π 1 2 e d i t 2 2 , 0 t < , d i > 0
considered by Haubold and Mathai [1].
From the lifetime density function given in Equation (34) and the mean lifetime Equation (38) we can infer that
  • the expected lifetime of the species depends on the value of c i and α. As c i ( 3 2 α ) increases the expected lifetime decreases and vice versa.
  • 1 c i ( 2 α ) f ( t ) Δ ( t ) can be interpreted as the amount of the net destruction in a small time interval Δ ( t ) . As the net destruction is faster the lifetime becomes smaller.

3. Connection of Extended Kinetic Equation to Fractional Calculus

Let Φ 1 ( t 1 ) be an integrable function as defined in Equation (34) and Φ 2 ( t 2 ) = θ ( t ) be any integrable function, then by the Mellin convolution property, we have
Φ ( u ) = t 1 t Φ 1 ( t ) Φ 2 ( u t ) d t = t 1 t Φ 1 ( u t ) Φ 2 ( t ) d t
Then Φ ( u ) , after substituting Φ 1 ( t 1 ) and Φ 2 ( t 2 ) , takes the form
Φ ( u ) = c i ( 2 α ) t = 0 1 t [ 1 + ( α 1 ) c i u t ] 1 α 1 θ ( t ) d t
for α > 1 which can be considered as a generalized fractional Kober type operator of an integrable function θ ( t ) . Here as α 1 we have
Φ ( u ) = c i ( 2 α ) t = 0 t 1 e c i u t θ ( t ) d t
More general cases can be seen in the paper Mathai and Haubold [15].

4. Fractional Kinetic Equation and Its Solution

The following discussion is based on [16,17]. In Equation (4), if instead of an ordinary classical integral we use a fractional integral, we get the reaction equation as
N ( t ) N 0 = c ν 0 D t ν N ( t ) , ν > 0
where 0 D t ν N ( t ) represents the Riemann-Liouville fractional integral defined as
0 D t ν f ( t ) = 1 Γ ( ν ) 0 t ( t u ) ν 1 f ( u ) d u , ν > 0
with 0 D t 0 f ( t ) = f ( t ) . Taking Laplace transform, simplifying and then taking the inverse Laplace transform one gets
N ( t ) = N 0 k = 0 ( 1 ) k ( c t ) k ν Γ ( 1 + k ν ) = N 0 E ν ( c ν t ν )
where E ν ( c ν t ν ) is the Mittag-Leffler function, introduced by M. G. Mittag-Leffler in 1903 [18] as
E β ( z ) = k = 0 z k Γ ( β k + 1 ) , β C , ( β ) > 0 , z C
If we consider a generalization of the fractional kinetic equation considered by Mathai, Haubold and Saxena [16,17] in the form
N ( t ) N 0 t ω 1 E ν , ω γ ( c ν t ν ) = c ν 0 D t ν N ( t ) , ν > 0 , ω > 0 , γ > 0
where E ν , ω γ ( . ) is the generalized three parameter Mittag-Leffler function introduced by Prabhakar [19] defined as
E β , ρ γ ( z ) = k = 0 ( γ ) k z k Γ ( β k + ρ ) k ! , β , ρ , γ C , ( β ) > 0 , ( ρ ) > 0 , z C
then the solution of the fractional kinetic Equation (49) is
N ( t ) = N 0 t ω 1 E ν , ω γ + 1 ( c ν t ν )

5. Conclusions

The linear and non-linear kinetic equations establish a connection between the Boltzmann-Gibbs statistical mechanics and Tsallis non-extensive statistical mechanics. The pathway parameter α plays a key role in switching between these two cases. The theory of extended reaction rates and its closed form solutions can be seen in Haubold and Kumar [10] and Kumar and Haubold [12]. Further, the fractional diffusion equation and its solution help us to understand the connection with the classical Laplace transform. In 2013, the author has solved the fractional kinetic equations discussed here by P α -transform [20]. Various fractional differential equations and their solution by various transforms are studied by many authors, see [21,22]. It should be noted that the Mittag-Leffler function arises in the solution of a fractional diffusion equation whereas the exponential function arises in the solution of its classical counterpart. A possible connection of the extended kinetic equation to fractional calculus can be established through the procedure adopted here.

Acknowledgments

The author acknowledges gratefully the encouragements given by Professor A. M. Mathai, Centre for Mathematical and Statistical Sciences, KFRI, Peechi, Kerala, and Hans J. Haubold, Chief Scientist, Office of Outer Space Affairs, Vienna, Austria in this research work. The author would also like to thank the unknown referees for their valuable suggestions which enhanced the paper in the present form.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Haubold, H.J.; Mathai, A.M. A heurisitc remark on the periodic variation in the number of solar neutrinos detected on Earth. Astrophys. Space Sci. 1995, 228, 113–134. [Google Scholar] [CrossRef]
  2. Haubold, H.J.; Mathai, A.M. The fractional kinetic equation and thermonuclear functions. Astrophys. Space Sci. 2000, 273, 53–63. [Google Scholar] [CrossRef]
  3. Mathai, A.M. A Pathway to matrix-variate gamma and normal densities. Linear Algebra Appl. 2005, 396, 317–328. [Google Scholar] [CrossRef]
  4. Mathai, A.M.; Haubold, H.J. Pathway model, superstatistics, Tsallis statistics and a generalized measure of entropy. Phys. A 2007, 375, 110–122. [Google Scholar] [CrossRef]
  5. Mathai, A.M. A Handbook of Generalized Special Functions for Statistical and Physical Sciences; Clarendo Press: Oxford, UK, 1993. [Google Scholar]
  6. Rainville, E.D. Special Functions; Chelsea Publishing Company: New York, NY, USA, 1960. [Google Scholar]
  7. Mathai, A.M.; Saxena, R.K.; Haubold, H.J. The H-function: Theory and Applications; Springer: New York, NY, USA, 2010. [Google Scholar]
  8. Meijer, C.S. Uber Whittakersche bzw. Besselsche Funktionen und deren Produkte. Nieuw Arch. Wiskd. 1936, 18, 10–39. [Google Scholar]
  9. Haubold, H.J.; Mathai, A.M. The Maxwell-Boltzmannian Approach to the Nuclear Reaction Rate Theory. Fortschr. Phys. 1985, 33, 623–644. [Google Scholar] [CrossRef]
  10. Haubold, H.J.; Kumar, D. Extension of thermonuclear functions through the pathway model including Maxwell-Boltzmann and Tsallis distributions. Astropart. Phys. 2008, 29, 70–76. [Google Scholar] [CrossRef]
  11. Haubold, H.J.; Kumar, D. Fusion yield: Guderley modeland Tsallis statistics. J. Plasma Phys. 2011, 77, 1–14. [Google Scholar] [CrossRef]
  12. Kumar, D.; Haubold, H.J. On extended thermonuclear functions through pathway model. Adv. Space Res. 2009, 45, 698–708. [Google Scholar] [CrossRef]
  13. Tsallis, C. Possible generalization of Boltzmann-Gibbs statistics. J. Stat. Phys. 1988, 52, 479–487. [Google Scholar] [CrossRef]
  14. Tsallis, C. Introduction to Nonextensive Statistical Mechanics: Approaching a Complex World; Springer: New York, NY, USA, 2009. [Google Scholar]
  15. Mathai, A.M.; Haubold, H.J. Erdélyi-Kober Fractional Integral Operators from a Statistical Perspective-I. 2013; arXiv:1303.3978. [Google Scholar]
  16. Saxena, R.K.; Mathai, A.M.; Haubold, H.J. On fractional kinetic equations. Astrophys. Space Sci. 2002, 282, 281–287. [Google Scholar] [CrossRef]
  17. Saxena, R.K.; Mathai, A.M.; Haubold, H.J. Unified fractional kinetic equation and a fractional diffusion equation. Astrophys. Space Sci. 2004, 209, 299–310. [Google Scholar] [CrossRef]
  18. Mittag-Leffler, G.M. Sur la nouvelle fonction Eα(x). CR Acad. Sci. Paris 1903, 137, 554–558. [Google Scholar]
  19. Prabhakar, T.R. A singular integral equation with a generalized Mittag-Leffler function in kernel. Yokohama Math. J. 1971, 19, 7–15. [Google Scholar]
  20. Kumar, D. Solution of fractional kinetic equation by a class of integral transform of pathway type. J. Math. Phys. 2013, 54. [Google Scholar] [CrossRef]
  21. Diethelm, K. The Analysis of Fractional Differential Equations; Springer: Berlin, Germany, 2010. [Google Scholar]
  22. Gorenflo, R.; Mainardi, F. Fractional calculus, integral and differential equations of fractional order. In Fractals and Fractional Calculus in Continuum Mechanics; Carpinteri, A., Mainardi, F., Eds.; Springer: Wien, Austria, 1997; pp. 223–276. [Google Scholar]

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Kumar, D. Some Aspects of Extended Kinetic Equation. Axioms 2015, 4, 412-422. https://doi.org/10.3390/axioms4030412

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Kumar D. Some Aspects of Extended Kinetic Equation. Axioms. 2015; 4(3):412-422. https://doi.org/10.3390/axioms4030412

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