Magnetocaloric Effect Caused by Paramagnetic Austenite–Ferromagnetic Martensite Phase Transformation

: In the present work, the magnetization of Ni 50 Mn 17.5 Ga 25 Cu 7.5 alloy undergoing the ﬁrst-order phase transition from paramagnetic austenite to ferromagnetic martensite was measured to evaluate the magnetic-ﬁeld-induced entropy change (MFIEC) and refrigerant capacity (RC) of the alloy. A standard method (SM) of evaluation of MFIEC is based on thermodynamic Maxwell relation. In view of the criticism of SM expressed by some scientists, the alternative method (AM), which is based on thermodynamic relationships for free energy, was proposed recently for the determination of MFIEC. We developed this method and computed MFIEC in two ways—by AM and SM. The values of MFIEC obtained for Ni 50 Mn 17.5 Ga 25 Cu 7.5 alloy by these methods appeared to be large but very different from each other. Moreover, AM reveals the possibility of both normal and inverse magnetocaloric effects in the adjoining temperature ranges, while SM results only in the normal magnetocaloric effect.


Introduction
The normal/inverse magnetocaloric effect (MCE) is the decrease/increase of the temperature of a solid in the presence of a decreasing or increasing magnetic field. The solid cooled under a variable magnetic field can absorb the heat from the environment, so magnetic materials exhibiting large MCEs can be used for the design of magnetic refrigerators. Magnetic shape memory alloys (SMAs) are among materials considered to be promising for application in magnetic refrigeration technology, and have, accordingly, been studied in detail [1,2].
To describe the heat transfer between a solid exhibiting MCE and the environment, the isothermal entropy change induced by the external magnetic field increasing from H 1 to H 2 is evaluated, usually from the equation where M(T, H) is the magnetization value in the magnetic material [3]. Equation (1) is a consequence of thermodynamic Maxwell relations; it shows that a large entropy change and most pronounced MCE should be expected in the temperature range corresponding to the abrupt change of magnetization value. This feature of magnetization behavior has attracted the attention of researchers to martensitic transformations (MTs) from ferromagnetic austenite to paramagnetic martensite, observed in the metamagnetic SMAs [1,2]. However, the abrupt change in magnetization also appears in the temperature range of first-order phase transformation of SMA, from paramagnetic austenite to ferromagnetic martensite [4][5][6]. Therefore, a theoretical estimation of the magnetic-field-induced entropy change for SMA undergoing such phase transformation may be a guide for experiments aimed at the improvement of magnetic refrigeration technology. However, sound arguments against the applicability of thermodynamic Maxwell relations to ferromagnetic solids undergoing first-order phase transitions were presented (see Refs. [1,7,8] and references therein). It was argued, firstly, that these relations were obtained for the equilibrium thermodynamic phase, and therefore, that they are not applicable to the mixed two-phase thermodynamic state arising in the temperature range of first-order phase transitions. It was found, secondly, that the MCE value strongly depends on the shift of phase transition temperature under magnetic field [9]. This feature of MCE obviously cannot follow from the equation obtained for the equilibrium thermodynamic phase. In this connection, other ways of evaluating MCE deserve careful attention.
In the present study, we analyze the possibility of evaluating MCE from the fundamental thermodynamic relationship which relates entropy function S to the temperature derivative of Helmholtz free energy F. The expression for free energy is a starting point of the Landau-type theories of magnetic, structural, and magnetostructural phase transitions. Due to this, Equation (2) was used recently for the evaluation of the magnetic-field-induced entropy change and heat capacity of metamagnetic SMA [10,11]. The free energy depends on temperature through the temperature-dependent magnetization value. Therefore, for the detailed theoretical analysis of MCE we used the experimental temperature dependences of magnetization of a Ni 50 Mn 17.5 Ga 25 Cu 7.5 alloy, which undergoes the phase transformation from paramagnetic austenite to ferromagnetic martensite. These dependences enabled the estimation of the MCE value not only from Equation (2), but from the Equation (1) as well. The function ∆S 1→2 (T) obtained using Equation (2) appeared to be qualitatively and quantitatively different from that computed from Equation (1). In this respect, the theory of the first-order magnetic phase transition presented in Ref. [12] should be mentioned. Comparing the predictions of the theory with the results obtained using the Maxwell relations, the author of this work concluded that these relations are applicable to the evaluation of the field-induced entropy change in the temperature range of the first-order magnetic phase transition with narrow temperature hysteresis, but that the phase transitions in multiferroic systems need special consideration. The SMAs belong to such systems.

Experimental
A polycrystalline alloy with nominal composition Ni 50 Mn 17.5 Ga 25 Cu 7.5 was prepared from high-purity elements by arc melting under Ar atmosphere. The ingots were homogenized in vacuum quartz ampoules at 1170 K for 24 h and quenched in water at room temperature. The actual composition of the homogenized alloy was determined by energy-dispersive X-ray spectroscopy (EDS, Bruker X-flash detector 4010, EDS, Bruker X-flash detector 4010, Bruker, Germany) in a scanning electron microscope (Hitachi S-3400 N, Hitachi S-3400 N, Hitachi, Japan), and shown to be Ni 49.3 Mn 17.8 Ga 25.2 Cu 7.7 . The temperature dependences of magnetization of this alloy measured for different values of external magnetic field are shown in Figure 1.

Model Formulation
Experimentally-measured magnetization of SMA, M exp (T, H), corresponds to magnetization of the austenitic phase at T > T MS and the martensitic phase at T < T MF . In the temperature range T MF < T < T MS , the experimentally-measured magnetization is the average value of magnetizations of coexisting microscopic domains of the austenitic and martensitic phases. To simplify the theoretical description of MCE, the average value of the magnetic exchange parameter J av (T, H) is used below. This value is expressed through the magnetic exchange parameters of austenitic, J aust (T), and martensitic, J mart (T), phases, and the volume fraction of martensite, α(T, H), which is equal to zero in the austenitic phase and to one in the martensitic phase. The free energy density of SMA is expressed as where The parameters J aust (T) and J mart (T) are not equal, because the PM austenite-FM martensite transformation is accompanied by the volume change of ferromagnetic SMA (FSMA) and the intensity of spin-exchange process drastically depends on the distances between the magnetic atoms. The magnetic exchange parameters are interrelated as where v MT is the relative volume change during MT, δ 0 is the magnetoelastic constant describing the volume magnetostriction, and M 2 0 is the sum of magnetic moments of atoms contained in the unit volume of SMA [13]. The volume fraction of martensite can be modeled by the function where This function qualitatively represents the experimental temperature dependence of the volume fraction of martensite measured for Ni 2 MnGa alloy with a MT temperature of about 210 K [14]. Therefore, Equations (3) and (4) describe the free energy of SMA at any temperature achievable in the experiments. The ferromagnetic ordering of austenitic phase appears when J aust (T) changes its sign, that is, at Curie temperature, T C . Thus, the equation J aust (T) = J 0 (T − T C )/T C is accepted in the Landau theory of phase transitions. To describe the first-order magnetic phase transition, the terms proportional to M 4 and M 6 must be included in the expression for the free energy F(T, H) [12]. In Ni-Mn-Ga-based alloys, the second-order PM−FM phase transitions are observed, so such terms can be omitted in Equation (3). The first-order character of the PM austenite−FM martensite phase transition is caused by the jump-like change of lattice parameters.
Equations (3), (4) and (6) illustrate a very important feature of the PM austenite-FM martensite transformation: the average value of magnetic exchange energy depends on the magnetic field not only through the magnetization value, but also through the volume fraction of martensite, which is involved in Equation (4) for the average value of exchange parameter. It should be emphasized, moreover, that the dependence of the exchange parameter on the magnetic field vanishes in the limiting case The magnetic-field-induced entropy change is expressed through the free energy as (One ought not to confuse the field-induced entropy change with the entropy change accompanying martensitic transformation.) According to Equation (3), the expression for the entropy change Equation (7) includes the terms, which are proportional to ∂M(T, H 1 )/∂T and −∂M(T, H 2 )/∂T. It may be expected that these summands give the main contribution to the field-induced entropy change in the temperature range of the phase transition, due to the abrupt change of magnetization value (see Figure 1).

Application of Simplified Model to Ni 50 Mn 17.5 Ga 25 Cu 7.5 Alloy
The magnetic-field-induced entropy change computed from Equations (2)-(7) using the experimental values M exp (T, H) measured in the fields µ 0 H 1 = 1 T and µ 0 H 2 = 7 T (see Figure 1) is presented by a dashed line in Figure 2. The wavy shape of this line is an artefact caused by the interpolation of experimental points performed by the software. The physical parameters used for computation are given in the Appendix A, and the mode of evaluation of these parameters is explained there. The meaning of the solid line is explained in Section 4.2.    the magnetic field of 7 T, that is, between the temperatures T MS (H 2 ) = 335.7 K and T MF (H 2 ) = 332.0 K (see also Figure 1). The entropy change can be positive as well, due to the quick change of magnetization M(T, H 1 ) in the temperature range of MT in the magnetic field of 1 T, that is, between the temperatures T MS (H 1 ) = 330.3 K and T MF (H 2 ) = 328.5 K. The point is that the temperature ranges of MT in the fields H 1 and H 2 do not overlap (T MF (H 2 ) > T MS (H 1 )), so the positive term S(T,H 2 ) in Equation (7) is not overcompensated by the negative term −S(T, The inverse MCE arises due to the shift of phase transition temperature under the magnetic field. This effect will be analyzed below in the course of a detailed theoretical analysis of the field-induced entropy change. Two important remarks are appropriate here: (i) The high magnitude of the entropy change −30 J kg −1 K −1 caused by the field change µ 0 ∆H = 5 T was reported for the La-Fe-Si compound, which exhibited magnetization behavior similar to that shown in Figure 2 [15].
(ii) An almost linear dependence of maximal value of the entropy change on the magnetic field has been reported (see Ref. [12] and references therein). Therefore, the high absolute value of negative entropy change, |∆S 1→2 (T)| ∼ 10 J kg −1 K −1 , which corresponds to strong "conventional" MCE, can be predicted for the moderate field change µ 0 ∆H = 1 T. It makes the alloys exhibiting a PM austenite-FM martensite phase transition promising for applications in magnetic refrigeration. The negative values of the entropy change are interesting because they point to possibility of inverse MCE. This possibility arises from the shift of MT temperature under a magnetic field, and does not follow from Equation (1) because the temperature derivative of magnetization is negative at all temperature and field values.

Theoretical Basis
For a detailed thermodynamic analysis of MCE observed during MT, one must take into account the fact that MT is a first-order phase transition, which goes through the mixed austenitic-martensitic state, and calculate the field-induced entropy change ∆S 1→2 from the free energies F aust and F mart of austenitic and martensitic phases, respectively. For this purpose, the theoretical magnetization functions M aust (T, H) and M mart (T, H) must be derived from certain physical considerations, and substituted into the expressions The free energy of the alloy, must be used then for the calculation of entropy change.
The function α(T, H), which models the volume fraction of martensite, depends on the martensite start and martensite finish temperatures. The experiments show that these temperatures almost linearly depend on the magnetic field, that is where dT MS,MF /dH are constants. In contrast to the equations of the simplified model, the values of magnetization and exchange parameter of the mixture of austenitic and martensitic domains are not involved in Equations (8) and (9) for the free energy of the alloy. Instead, the free energy is expressed through the individual characteristics of mixed phases J aust (T), J mart (T), M aust (T, H) and M mart (T, H). This is an appreciable Metals 2019, 9, 11 6 of 13 difference between the simplified model and the theory in question. Therefore, the equations describing the magnetization functions M aust (T, H) and M mart (T, H) of the austenitic and martensitic phases must be used for the evaluation of the field-induced entropy change. As shown in Refs. [13,16], a quantitative agreement between the theoretical and experimental temperature dependences of magnetization in the saturating magnetic field ∼ 1 T could be achieved starting from the conception of the local Curie temperatures T C (n) attributed to small spatial domains of FSMA. (The integer n = 1, 2, . . . N enumerates the spatial domains.) The difference between the local temperatures is assumed to be caused by the difference in the values of magnetic exchange parameters inherent to different domains. It was found empirically that the temperature dependences of magnetization measured in strong magnetic fields (~2-10 T) can be described by the introduction of field-dependent parameters involved into the equations for magnetization value M(T, H, n) in the nth spatial domain being in the austenitic or martensitic state, respectively. According to the fundamentals of phase transitions theory, these parameters are not the phase transition temperatures from the paramagnetic to ferromagnetic phase, but they satisfactorily describe the temperature dependences of heat capacity and entropy change if the constant parameter ∆ T is adjusted properly by fitting the theoretical magnetization values to experimental ones [10,11]. The magnetization values in the nth spatial domain of alloy, which undergoes phase transformation, are expressed by the standard equation with T C (H, n) = T CA (H, n) for austenitic phase, or T C (H, n) = T CM (H, n) for martensitic phase.
The small spatial domains of alloy contribute to the magnetization values involved in Equation (9) for the free energy with different statistical weights p(n). The difference in statistical weights is caused by the difference in the volume fractions of spatial domains with different Curie temperatures. The computations performed previously for the Ni-Mn-Ga alloys showed that the theoretical temperature dependence of magnetization could be fitted to experimental one using the Gauss-like distributions of statistical weights where The terms depending on the "ordinary" magnetic susceptibility of the austenitic and martensitic phases, χ(T), are included into Equation (14). These terms are not of principal importance, but they increase the accuracy of fitting theoretical magnetization curves to experimental ones.
Equations (3)-(13) enable the study of MCE caused by martensitic transformations of FSMAs with different MT temperatures and Curie points. Formally, the magnetostructural phase transformation from paramagnetic austenite to ferromagnetic martensite corresponds to the Curie point of martensite situated above MT temperature.

MCE in Ni 50 Mn 17.5 Ga 25 Cu 7.5 Alloy
The experimental temperature dependences of magnetization depicted in Figure 3 show that the Curie point of Ni 50 Mn 17.5 Ga 25 Cu 7.5 alloy is situated not far from the MT temperature range.
increase the accuracy of fitting theoretical magnetization curves to experimental ones.
Equations (3)-(13) enable the study of MCE caused by martensitic transformations of FSMAs with different MT temperatures and Curie points. Formally, the magnetostructural phase transformation from paramagnetic austenite to ferromagnetic martensite corresponds to the Curie point of martensite situated above MT temperature.

MCE in Ni50Mn17.5Ga25Cu7.5 Alloy
The experimental temperature dependences of magnetization depicted in Figure 3 show that the Curie point of Ni50Mn17.5Ga25Cu7.5 alloy is situated not far from the MT temperature range.   (8)) and the free energy of alloy undergoing the MT through the mixed austenitic-martensitic state (Equation (9)). It should be stressed that M av (T, H) is not used for the computation of free energy and entropy change; it is needed only for the determination of physical values involved in Equations (12)- (14). However, the M av (T, H) values are plotted in Figure 3 as the functions of temperature to illustrate the accuracy of theoretical description of MCE presented below. Figure 4a shows the values of magnetic entropy and field-induced entropy change computed from Equations (7)-(9) for two field values, µ 0 H 1 = 1 T, µ 0 H 2 = 7 T, and different temperatures. The computations were carried out using the theoretical temperature dependences of magnetization, M mart (T, H 1,2 ), M aust (T, H 1,2 ), expressed by Equation (14). The entropy change shown in Figure 4a is presented also in Figure 2 to illustrate the accuracy of simplified model of MCE.
The behavior of magnetic entropy functions is in agreement with fundamental principles of thermodynamics, namely: (i) The value S(0, 0) is equal to zero, because in general an entropy function is unique up to a constant, and therefore, one can put S(0, 0) = 0 (in agreement with the third law of thermodynamics).
(ii) The magnetic entropy functions S(T, H 1,2 ) are negative, because the magnetic free energy is negative in ferromagnetic phase (as far as it is lower than the energy of paramagnetic phase), its absolute value decreases with temperature, and therefore, the value −∂F/∂T = ∂|F|/∂T is positive. austenitic-martensitic state (Equation (9)). It should be stressed that av ( , ) M T H is not used for the computation of free energy and entropy change; it is needed only for the determination of physical values involved in Equations (12)- (14). However, the av ( , ) M T H values are plotted in Figure 3 as the functions of temperature to illustrate the accuracy of theoretical description of MCE presented below. Figure 4a shows the values of magnetic entropy and field-induced entropy change computed from Equations (7)-(9) for two field values, 01 (14). The entropy change shown in Figure 4a is presented also in Figure 2 to illustrate the accuracy of simplified model of MCE.   Figures 2 and 4a is an unforeseen prediction of the theory, which points to possibility of both conventional and inverse MCE in different temperature ranges, while the M(T) function is monotone in this temperature range. (The observation of "neighboring" conventional and inverse magnetocaloric effects in metamagnetic SMAs is caused by the nonmonotonic change of M(T) below the Curie temperature [17][18][19].) This result follows from two features of Ni 50 Mn 17.5 Ga 25 Cu 7.5 alloy: first, the noticeable field-induced shift of MT temperature (~5 K), and second, abrupt change of large magnetization value M(T, H 1 ) during MT. These features result in the positive contribution −S(T, H 1 ) to the field-induced entropy change, which is not overcompensated by the negative term S(T, H 2 ). In this connection, one more peculiarity of experimental dependences M(T, H 1 ) and M(T, H 2 ) should be noted: the change of M(T, H 2 ) during MT is smaller than the change of M(T, H 1 ), because of the huge contribution of the magnetic field H 2 = 7 T to magnetization value measured above MT temperature (see Figure 3). This peculiarity may be explained by the field-induced shift of MT temperature in the case of the "paramagnetic Curie temperature" of austenite, which is involved in the Curie−Weiss low, and is lower but close enough to MT temperature. In this case, the magnetic field of 7 T approaches the MT temperature to the maximum point of magnetic susceptibility of austenite and therefore induces large magnetization value.
The magnetic-field-induced entropy change ∆S 1→2 resulting from Equations (8)- (14) is shown in Figure 4a and represented by solid line in Figure 2 to illustrate the quantitative agreement between the predictions of the simplified model and detailed analysis of MCE. In this relation, it should be emphasized that both the simplified model and detailed analysis are based only on three principal points, namely, (i) the experimentally-observed shift of MT temperature under a magnetic field, (ii) the relationship between the entropy and free energy (Equation (2)), and (iii) the expression for the magnetic free energy of a ferromagnetic solid (Equations (3) and (8)). It should be emphasized that the Equation (2) is one of fundamental relationships of thermodynamics; the Equations (3) and (8) are derived from the quantum mechanical Heisenberg expression for the Hamiltonian describing the spin-exchange interaction and from the fundamental electrodynamic equation for the energy of magnetic moment in an external magnetic field. Therefore, the predicted possibility of the observation of conventional and inverse MCE in two neighboring temperature intervals is well-grounded, and may be considered as a guide for experiments. One of the obstacles to the observation of inverse MCE may be related to the narrow (~2-5 K) temperature interval of negative entropy change (see Figure 2). However, this difficulty is surmountable: conventional and inverse MCE were observed in Ni 50 Mn 35 In 15 in the narrow temperature interval~10K [17][18][19].

MCE in the Ni 50 Mn 18 Ga 25 Cu 7 Ribbon
The detailed experimental study of the transformational behavior and magnetic properties of a Ni 50 Mn 18 Ga 25 Cu 7 ribbon was carried out in Ref. [5] and the maximum value ∆S max 1→2 = 17.8 J kg −1 K −1 was reported. Experimental data presented in this work enable an additional verification of the theory developed above. The magnetization values determined in Ref. [5] for µ 0 H = 5 T provide the physical parameters needed for the detailed theoretical description of MCE (see Appendix A). These parameters result in a good fit of the theoretical magnetization curve to experimental values obtained in the field µ 0 H 2 = 5 T, and enable the computation of temperature dependences of magnetization for the other field values, in particular, µ 0 H 1 = 1 T. Figure 5 shows the entropy functions, S(T, H 1 ), S(T, H 2 ), and field-induced entropy change ∆S 1→2 (T) computed using the magnetization curves shown in the Inset. The entropy functions noticeably depend on temperatures in the range shown in Figure 5, but become almost constant in the low-temperature range (below 200 K), where the magnetization value is close to its low-temperature limit M(0, 0) = 400 G. It should be stressed, first, that the maximal entropy change resulting from computations (19.8 J kg −1 K −1 , see Figure 5) is close to the experimental value 17.8 J kg −1 K −1 reported in Ref. [5]. (This fact may be considered as verification of the results obtained from the thermodynamic relationship for the free energy, Equation (2)). Secondly, it is important that the computations performed for Ni 50 Mn 18 Ga 25 Cu 7 ribbon do not point to the possibility of inverse MCE because of the smooth variation of M(T, H 1 ) function, and, correspondingly, feebly-marked minimum of the entropy.

Comparison of Obtained MCE Values with Evaluation Resulting from Maxwell Relations
The good fit of theoretical M(T, H 1 ) and M(T, H 2 ) curves to experimental magnetization values obtained for Ni 50 Mn 17.5 Ga 25 Cu 7.5 alloy encourage the use of theoretical magnetization values, M(T n , H), for evaluation of magnetocaloric effect from Equation (1), which results from Maxwell relations. These functions have been computed from Equations (12)- (15) for the discrete temperature values T n , with the step T n − T n−1 = 1 K and substituted into Equation (1). In such a way, the discrete values of the field-induced entropy change ∆S 1→2 (T n ) have been computed from this equation by the integration of theoretical functions M(T n , H) from µ 0 H 1 = 1 T to µ 0 H 2 = 7 T with the integration step of 0.01 T. These values are shown in Figure 6 by the open circles; the connecting line serves merely as a guide for eye. The increase of the integration step by factor 10 did not noticeably change the result of integration. The function obtained above from Equations (2) and (7) is represented in Figure 6 for reference, and thus, the drastic difference between the MCE values obtained from these equations, on one hand, and Equation (1), on the other hand, is illustrated.  (1) and Equations (2) and (7). The vertical arrows point to the temperatures used for estimation of refrigerant capacity (see Equation (16)).

Refrigerant Capacity
The practically important parameter of MCE is the refrigerant capacity (RC), which is most commonly defined as where the temperatures 1 T and 2 T correspond to the half-maximum values of 12 () ST   function [20]. However, for the comparison of two ways of estimating MCE, it is more instructive to have these temperatures equal to the 1 326 K T  and 2 337 K T  , because these temperatures bound the temperature interval of large absolute values of entropy changes computed in two different ways, that is, from the Maxwell relationship and from the free energy (as shown in Figure 6 by the vertical arrows  Figure 6, because in our theory, the positive contribution to refrigerant capacity partially compensates for the negative one.

Discussion and Conclusion
The disagreement between the results obtained from Equations (1) and (2) is not completely clear from a physical point of view. To become aware of the formal reasons for the difference, let us recall that the results of the simplified model, which uses free energy with average values of magnetization and magnetic exchange parameter, appeared to be in agreement with the findings of the detailed analysis, which uses the free energies and magnetization values of two phases. Therefore, the difference between the 12 () ST   and 12 () n ST   curves, shown in Figure 6, arises not from the averaging of physical values over the domains of two phases; rather, it arises, firstly, because the integration in finite terms, 1 H , 2 H , predetermined by Equation (1), smooths over the influence of two functions,   (1) and Equations (2) and (7). The vertical arrows point to the temperatures used for estimation of refrigerant capacity (see Equation (16)).

Refrigerant Capacity
The practically important parameter of MCE is the refrigerant capacity (RC), which is most commonly defined as where the temperatures T 1 and T 2 correspond to the half-maximum values of ∆S 1→2 (T) function [20]. However, for the comparison of two ways of estimating MCE, it is more instructive to have these temperatures equal to the T 1 = 326 K and T 2 = 337 K, because these temperatures bound the temperature interval of large absolute values of entropy changes computed in two different ways, that is, from the Maxwell relationship and from the free energy (as shown in Figure 6 by the vertical arrows). In this case, the refrigerant capacity calculated from the ∆S(T) curve estimated from Maxwell relations is RC ≈ − 100 ± 5 J/kg, while the simplified model and detailed analysis give RC ≈ − 160 ± 5 J/kg. Thus, the relative difference in RC values is much smaller than the relative difference of maximum values of ∆S 1→2 (T) functions shown in Figure 6, because in our theory, the positive contribution to refrigerant capacity partially compensates for the negative one.

Discussion and Conclusion
The disagreement between the results obtained from Equations (1) and (2) is not completely clear from a physical point of view. To become aware of the formal reasons for the difference, let us recall that the results of the simplified model, which uses free energy with average values of magnetization and magnetic exchange parameter, appeared to be in agreement with the findings of the detailed analysis, which uses the free energies and magnetization values of two phases. Therefore, the difference between the ∆S 1→2 (T) and ∆S 1→2 (T n ) curves, shown in Figure 6, arises not from the averaging of physical values over the domains of two phases; rather, it arises, firstly, because the integration in