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On-line version ISSN 1678-4618
Eclet. Quím. vol.31 no.1 São Paulo 2006
Comportamento térmico da decomposição de alguns complexos metálicos de poliditiooxamidas
H. Al-MaydamaI; A. El-Shekeil*; M. A. KhalidII; A. Al-KarboulyIII
IChemistry Department, Faculty of Science, Sana'a University, P. O. Box 12463, Sana'a, Yemen
IIPhysics Department, Faculty of Science, Sana'a University, P. O. Box 12463, Sana'a, Yemen
IIIChemistry Department, Faculty of Science, Anbar University, Khalidiya, Iraq
The thermal decomposition behavior of the Fe(II), Co(II), Ni(II) and Zn(II) complexes of polydithiooxamide has been investigated by thermogravimetric analysis (TGA) at a heating rate of 20°C min-1 under nitrogen. The Coats-Redfern integral method is used to evaluate the kinetic parameters for the successive steps in the decomposition sequence observed in the TGA curves. The processes of thermal decomposition taking place in the four complexes are studied comparatively as the TGA curves indicate the difference in the thermal decomposition behavior of these complexes. The thermal stabilities of these complexes are discussed in terms of repulsion among electron pairs in the valence shell of the central ion and electronegativity effects.
Keywords: polydithiooxamide-complexes; thermal behaviour; kinetic parameters; thermal stability.
O comportamento térmico da decomposição dos complexos de poli-ditiooxamidas de Fe(II), Co(II), Ni(II) e Zn(II) foi estudado por termogravimetria (TG), com razão de aquecimento de 20°C min-1 sob atmosfera de nitrogênio. O método integral de Coats-Redfern foi usado para calcular os parâmetros cinéticos das etapas sucessivas da decomposição observada nas curvas TGA. Os processos de decomposição térmica observados nos quatro complexos foram comparados e as suas respectivas estabilidades térmicas foram discutidas em função da repulsão entre os pares de elétrons da camada de valência do íon central e dos efeitos da eletronegatividade.
Palavras-chave: complexos de poliditiooxamidas; comportamento térmico; parâmetros cinéticos; estabilidade térmica.
The well-established thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) techniques have been reliably widely used over many decades in studying the thermal behaviour and properties of various types of materials and evaluating the thermal parameters for their degradation processes. These methods have allowed determination of the chemical steps of the investigated degradation and the evaluation, by some methods [1, 2], of the kinetic parameters for each step. The evaluation of the kinetic parameters has been often performed by using a single thermogravimetric curve (TG curve) recorded at a certain heating rate and atmospheres (under nitrogen or air flow).
Some recent results concerning the thermal and thermo-oxidative degradation of polymers or polymeric material, metal complexes, medicinal plant leaves and thermoplastic starch obtained by thermoanalytical methods (TG, DTG, DTA, DSC) have been reported [3 14]. These reports show that the kinetic parameters evaluated for each step of degradation processes are carried out by using the integral methods considering a reaction order model for the kinetic analysis of the a single thermogravimetric curve data.
In our previous studies published elsewhere , the temperature variation of the DC electrical conductivity was measured in the range 298 498 K for the polymer-metal complexes under investigation in the present work, and as a result the activation energies for different temperature segments were worked out. For the reason that a change in the composition may lead to changes of the measured electrical quantities (i.e. the role of adsorbed water), the thermal analysis results (TGA curves) were used only to monitor the loss of adsorbed water in order to study its effect on the DC electrical conductivity at 298 498 K range.
In this work, we illustrate a comparative study of some polymer-metal complexes of a particular ligand with various metals from the point of view of the thermogravimetric analysis (TGA) and its thermal parameters at a give condition (i.e. heating rate of 20°C min-1 under nitrogen). The chosen organic compound, dithiooxamide, is rich in electrons due to the existence of nitrogen and sulphur atoms forming the desired polydithiooxamide-metal complexes (PDTA) wherein the metal ion is placed in the backbone chain itself. In other words, the metal ion is the connecting link between the organic units in the linear chain, i.e. polymerization through coordination with the metal ion. We have chosen for the complex-ion the 3d-transition elements: Fe(II), Co(II), Ni(II) and Zn(II). The processes of thermal degradation taking place in these polymer-metal complexes have been investigated by thermogravimetric method (TG, DTG) and Coats-Redfern integral method  has been used to determine the associated kinetic parameters for the successive steps in the decomposition sequence. Although these four polymer-metal complexes are identical in terms of the ligand type around the metal ions of Fe(II), Co(II), Ni(II) and Zn(II), the difference in thermal decomposition behaviour and that in thermal stability are clearly observed.
Therefore, information concerning the thermal decomposition behaviour, thermal stability, mechanism and kinetics of the investigated degradation process obtained from the TG curves recorded for the four conducting polymer-metal complexes at a certain condition (i.e. heating rate of 20°C min-1 and nitrogen flow) has become of interest to be studied comparatively.
Synthesis of polymer complexes and physical analysis
Complete details of the synthesis, physical measurements, characterization and identification as well as the DC electrical conductivity of the three conducting polymer complexes of interest (PDTA-Fe, PDTA-Co, PDTA-Ni and PDTA-Zn) and their structure shown in structure 1 are published elsewhere .
The TG and DTG curves were obtained by using, Perkin-Elmer thermogravimetric Analyzer at a heating rate of 20°C min-1 under nitrogen flow and heating programme 30 800°C.
From the TG and DTG curves recorded for the successive steps in the decomposition process of these polymer complexes it was possible to determine the following characteristic thermal parameters for each reaction step:
Initial point temperature of decomposition (Ti): the point at which DTG curve starts deviating from its base line.
Final point temperature of decomposition (Tf): the point at which DTG curve returns to its base line.
Peak temperature, i.e. temperature of maximum rate of weight loss (TDTG): the point obtained from the intersection of tangents to the peak of DTG curve.
Mass loss at the decomposition step (Dm): it is the amount of mass that extends from the point Ti up to the reaction end point Tf on the TG curve, i.e. the magnitude of the ordinate of a TG curve. The material released at each step of the decomposition is identified by attributing the mass loss (Dm) at a given step to the component of similar weight calculated from the molecular formula of the investigated complexes, comparing that with literatures of relevant compounds considering their temperature. This may assist identifying the mechanism of reaction in the decomposition steps taking place in the polymer complexes under study.
Activation energy (Ea) of the composition step: the integral method used is the Coats-Redfern equation  for reaction order n ¹ 1, which when linearised for a correctly chosen n yields the activation energy from the slop;
where: a = fraction of weight loss, T = temperature (K), n = order of reaction, Z = pre-exponential factor, R = molar gas constant, Ea = activation energy and q = heating rate.
Order of reaction (n): it is the one for which a plot of the Coats-Redfern expression gives the best straight line among various trial values of n that are examined relative to that estimated by the Horovitz-Metzger method .
Results and discussion
The thermogravimetric (TG) and derivative thermogravimetric (DTG) curves, which characterize the thermal decomposition of the Fe(II), Co(II), NI(II) and Zn(II) complexes of polydithiooxamide (PDTA) in nitrogen atmosphere at a heating rate of 20°C min-1 are given in Figure 1. These curves show clearly the difference in the thermal decomposition behaviour of these polymer-metal complexes and the results are summarized in Table 1. Close examination of the TG / DTG curves (Fig. 1) reveals that with overlapping steps being various, a two-step decomposition process for PDTA-Zn complex at the 132-746°C range, a three-step process for PDTA-Fe complex at the 30-587°C range, a four-step for PDTA-Co complex at the 40-600°C and a five-step for PDTA-Ni complex at the 40-784°C range. It seems that the overlapping steps increase as the electronegativety of the metals increases; Ni > Co > Fe > Zn.
Table 1 compares the characteristic thermal and kinetic parameters determined or evaluated, from the TG curves, for each step in the decomposition sequence of the complexes. It can be seen clearly (Table 1) that the mass losses obtained from the TG curves and that calculated for the corresponding molecule or molecules are in good agreement as is the case for all of these complexes. However, as the compositions of the final decomposition products (i.e. final residues) are not proved, ill-defined final states are considered for the thermal decomposition of these four complexes. The activation energies (Ea) are calculated from the slopes of the best fit straight lines obtained when the plots of the Coats-Redfern equation  are used for the best values of reaction order (n).
The first-steps of decomposition in the TG curves at the 30-140°C, 40-163°C and 40-190°C range with their temperatures of maximum rate of weight loss (TDTG) in the DTG curves (Fig 1a,b,c) at 87 °C, 88 °C and 90°C indicate the loss of half molecule, one and half molecules and three molecules of water of crystallization in the Fe, Co and Ni-polymer complexes, respectively. This corresponds well with weight loss data for Fe (found 3.60%, cal 3.52%), Co (found 9.68%, cal 9.75%) and Ni polymer complex (found 17.54%, cal 17.79%). Dehydration of adsorbed water is not observed in the case of Zn complex. The temperature ranges reported [17-19] for releasing adsorbed water in some metal complexes are in good agreement with that mentioned above. The activation energy determined for these reactions in the polymer complexes of Fe, Co and Ni are 50.8 kJ mol-1, 48.5 kJ mol-1 and 49.1 kJ mol-1, respectively. Their temperature ranges and order of reaction (1.1, 1.7 and 2.6 for the Fe, Co and Ni complexes respectively) slightly vary (Table 1).
In this dehydration process, the ease of water desolvation (30°C < T < 190°C) in these complexes suggests that the water molecules are trapped in the crystal voids and make no contribution to the lattice forces [20, 21]. The small differences in the TDTG values (87, 88 and 90°C for the Fe, Co and Ni complexes, respectively) and that in the values of the activation energies (50.8, 48.5 and 49.1 kJ mol-1 for Fe, Co and Ni complexes, respectively) suggest that the water in these complexes may be identical, i.e., play similar little or no role in holding the crystal together.
The first-step of the PDTA-Zn complex decomposition occurs at the 132-273°C range (Fig 1d) with a very large and strongly sharp peak (TDTG) at 239°C indicates a rapid and vigorous decomposition feature. This step is accompanied by 54.23% weight loss recorded on the TG curve (Fig 1d) which may be accounted for by the evolution of two chloride atoms along with the decomposition of 56.71% of the backbone components (cal. 54.22%). The activation energy (136.1 kJ mol-1) is determined for the reaction of this step.
In the contrary, the second-step of Zn-complex (Fig 1d) at the 273-746 °C range, with a small and weak TDTG (699°C) due to extremely slow bleed of 20.38% weight loss, corresponds to the elimination of the remaining 43.29% of the backbone components (cal. 20.29%). The total mass loss up to 746°C leaves a 25.39% residual weight, which is in agreement with the final product (cal. 25.49%) at the end of the Zn-complex decomposition with an ill-defined final state. The activation energy (23.40 kJ mol-1) is determined for the reaction at this second step.
The TG curve of the PDTA-Fe complex (Fig 1a) suggests that the weight loss (57.37%) of a rapid decomposition at the second-step (153-397°C) with a very large and strong TDTG (293°C), and consecutively the weight loss (17.25%) of a gradual decomposition at the third-step (397-587°C) with a small and broad TDTG (468°C). These correspond to the co-evolution of two chlorine atoms with 63.35% of the backbone components (cal 57.45%) and the elimination of the remaining 36.65% of the backbone components (cal. 17.22%), respectively. The final residual weight found (21.78%) is referred to an ill-defined final product (cal 21.82%) at the end of the Fe-complex decomposition. The following activation energies; 39.20 kJ mol-1 and 167.60 kJ mol-1 are calculated for the second and third steps in the sequential decomposition of the PDTA-Fe complex, respectively.
From the TG curve of the PDTA-Co complex (Fig. 1b), four steps in the decomposition sequence are observed. The second and third steps in the (170-370°C) range clearly appear as consecutive and overlapping steps. The weight loss (12.84%) at the second-step (170-300°C) with a weak and very broad peak (TDTG) at 262°C suggests a very slow evolution of one chlorine atom (cal 12.80%). This temperature range is within the acceptable limit to that reported for the release of chlorine in some complexes of cobalt [18, 20, 22]. However, the weight loss (27.67%) at the third-step (300-370°C) with a large and strongly sharp peak TDTG at 333°C indicating a rapid and vigorous decomposition for the co-evolution of the second chlorine atom with 34.14% of the backbone components (cal 27.61%). The activation energies 90.6 kJ mol-1 and 293 kJ mol-1 are determined for the second and third steps.
The fourth-step (370-600°C) with a small and weak TDTG (533°C) indicates that the weight loss (found 15.16%, cal. 15.07%) is due to a very slow elimination of 34.74% of the backbone components. The total mass loss up to 600°C is in agreement with the relative magnitude (found 34.84%, cal. 34.77%) of an ill-defined final residue of the Zn-complex decomposition. The activation energy (120.40 kJ mol-1) is determined for this step.
Unlike the others, the TG curve (Fig 1c) for the Ni-complex decomposition shows five steps, with the second, third and fourth being overlapping steps at the peaks (TDTG) 284°C, 348°C and 390°C , respectively. These three overlapping steps are consequent upon three rapid and consecutive decomposition processes. Therefore, the Ni-complex losses its first chlorine atom (cal. 11.67%) at the second step (190-300 °C), and the second one (cal. 11.67%) at the third step (300-372°C) and then followed by the loss of 26.66% of the backbone (cal. 10.55%) at the fourth step (372-452°C). This corresponds to 11.79%, 11.64% and 10.71% weight losses from the TG curve (Fig. 1c) for these three consecutive and overlapping steps in the (190-452°C) range, respectively. The temperatures (270°C, 315°C, 220-374°C, 217-291°C and 330°C) reported for the release of chlorine atom in some nickel complexes [18, 20, 23, 24] are in accordance with that obtained. The activation energies (53.8 kJ mol-1, 206.2 kJ mol-1 and 400.1 kJ mol-1) are determined for the second, third and fourth step reactions, respectively.
A large and a very broad peak (TDTG) at 661°C for the fifth-step (478-784°C ) weight loss (21.11%) is attributed to the gradual elimination of 53.34% of the backbone components (cal 21.10%). The final residual weight found (27.15%) corresponds to an ill-defined final product (cal 27.22%) at the end of the Ni-complex decomposition. The activation energy (110.9 kJ mol-1) is obtained for this slow reaction at the fifth-step.
As preceded, the complex of cobalt and that of nickel both lose their two chlorine atoms in two steps. In case of nickel complex one chlorine atom in each step is observed. The second-step of the Co-complex and of the Ni-complex assigned for the release of one chlorine atom are comparable with each other in terms of their temperature range and temperature peak (TDTG), but their order of reaction and activation energies are incomparable. This reflects the kinetic difference and nature of these two molecules at the transition-state, i.e. their activated molecules are of different reaction nature. Therefore, rapid elimination of the chlorine atom with the lower activation energy (53.8 kJ mol-1) is observed in case of the Ni-complex, while in case of the Co-complex slow elimination of chlorine atom with the higher activation energy (90.6 kJ mol-1) is observed.
On the other hand, the thermal stability of these four polymer-metal complexes under investigation is discussed here on the basis of the starting point (i.e. initial temperature) of the first decomposition reaction which alters the multiple-bonding (six bonds) to a lower coordination numbers in the valence shells of the central ions. Hence, as the initial temperature (Ti) of the decomposition peak (Table 1) is taken as a measure of the thermal stabilities of these complexes, the following may be concluded:
The nickel complex shows a higher thermal stability (190°C) than those of cobalt (170°C), iron (153°C) and zinc (132°C) and this seems to be in accordance with the increasing values of the elecronegativity in the following order Ni > Co > Fe > Zn and decreasing ionic size Ni < Co < Fe =Zn. However, these initial temperatures (190°C, 170°C, 153°C,132°C for the complexes of Ni, Co, Fe, and Zn, respectively) generally suggest a low thermal stability feature for these complexes. This may be due to a high repulsion among the multiple-bonding (six bonds) electron pairs in the valence shells of these complex-ions, while the small and close differences (20°C, 17°C, and 21°C; Ni-Co, Co-Fe and Fe-Zn, respectively) show no steric effect as they have only two chelate rings.
Furthermore, it is noteworthy that in the situation of lower coordination numbers where the repulsion between the electron pairs in the valence shall of the central ion is decreased, the electronegativity of the central metal seems to become the predominant factor in the stability. This is observed in the backbone decomposition of the cobalt and nickel complexes of lower coordination numbers that are produced after losing their chlorine atoms individually. As the Co-complex loses its first chlorine atom and the Ni-complex loses its two chlorine atoms, they become of lower coordination numbers as five and four-bonding electron pairs in the valence shell of the cobalt and nickel ions, respectively. In fact, the nickel of the higher electronegativity and smaller ionic size unlike the others becomes of a five and four-bonding by losing its chlorine atoms successively as degradation proceeds. Hence, if the stability of the backbone with respect to the lower coordination numbers is considered, the nickel complex shows a higher thermal stability (372°C) for the initial decomposition of the backbone components, and a high thermal stability (300°C) for the cobalt complex is observed. These high thermal stabilities of the nickel and cobalt complexes perhaps suggest the electronegativity as the predominant factor. However, the thermal stability difference (72°C) between these two complexes explains the difference in the repulsion between the electron pairs in the five-bonding and that in the four-bonding of the cobalt and nickel complexes, respectively, i.e. higher repulsion in the five than that in the four-bonding electron pairs, and also considering the electronegativity difference between nickel and cobalt.
The results obtained from the TG and DTG curves (Table 1) confirm the hydration degree and the stoichiometry of the prepared PDTA metal complexes (structure 1) that are established  by elemental analysis (CHN analyzer) and metal content measurements (Atomic absorption Spectrophotometer). In addition to that, although these polymer-metal complexes are of a particular ligand with various metals, various thermal decomposition behaviour and thermal stability are clearly observed. This may be attributed to the differences in the electronegativity values of the metals.
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Recebido em: 05/12/2005
Aceito em: 08/03/2005