a06v33n1.pdf Introduction Benzoic acid and some of its derivatives are used as conservant, catalyst polymers precur- sors, in pharmaceutical industries, etc. A survey of literature shows that the complexes of rare earth elements with benzoic acid and some of their derivatives have been investigated in aque- ous solutions [1-5] and in solid state [6-25]. In the present study, as an extension of the work of ref. 25, benzoates of trivalent lanthanides and yttrium (III) were investigated by using simultaneous thermogravimetry and differential thermal analysis (TG-DTA) in a CO2 atmosphere. The results of this study are discussed in connec- tion with those found for previously study involv- ing these compounds in an air atmosphere. Experimental The preparation of the solid state compounds of trivalent lanthanides and yttrium (III) with Bz, as well as, the determination of hydration water, metal- lic ions and ligand contents, the same procedure were used as previously described in Ref. 25. The Simultaneous TG-DTA curves were obtained with thermal analysis system model SDT 2960 from TA Instruments. The purge gas was a CO2 with flow of 100 mL min-1. A heating rate of 20 ºC min-1 was adopted with samples weighing about 7 mg. Alumina crucibles were used for TG-DTA. Results and Discussion The analytical and thermoanalytical (TG) data were obtained in air atmosphere, Table 1 Ref. 25. These results establish the stoichiometry of these compounds, which are in agreement with the Ln(Bz)3.nH2O general formula, where Ln represents trivalent lanthanides or yttrium, Bz is benzoate and n= 2.5 (Nd), 2 (La, Ce, Pr, Sm), 1.5 (Eu, Gd), 1(Tb), 0.5 (Dy) and 0 (Ho to Lu and Y). The simultaneous TG and DTA curves of the compounds are shown in Fig. 1. These curves exhibit mass loss in steps and endothermic peaks 43Ecl. Quím., São Paulo, 33(1): 43-48, 2008 www.scielo.br/eq www.ecletica.iq.unesp.br Volume 33, número 1, 2008 Thermal decomposition of solid state compounds of lanthanide and yttrium benzoates in CO2 atmosphere J. R. Locatelli1, A. B. Siqueira2, C. T. Carvalho2, M. Ionashiro2* 1Academia da Força Aérea, AFA. Estrada de Aguaí; s/n, CEP 13630-000 Pirassununga, SP, Brazil. 2Instituto de Química, UNESP, C. P. 355, CEP 14801 – 970 Araraquara, SP, Brazil *massaoi@yahoo.com.br Abstract: Solid-state Ln-Bz compounds, where Ln stands for trivalent lanthanides and Bz is benzoate have been synthesized. Simultaneous thermogravimetric and differential thermal analysis in a CO2 atmosphere were used to study the thermal decomposition of these compounds. Keywords: lanthanides; benzoate; thermal decomposition; CO2 atmosphere. 44 Ecl. Quím., São Paulo, 33(1): 43-48, 2008 Figure 1. TG-DTA curves of the compounds: (a) La(L)3.2H2O (m = 7.014 mg), (b) Ce(L)3.2H2O (m = 6.937 mg), (c) Pr(L)3.2H2O (m = 7.156 mg), (d) Eu(L)3.1.5H2O (m = 6.806 mg), (e) Gd(L)3.1.5H2O (m = 7.022 mg), (f) Ho(L)3 (m = 7.062mg), (g) Yb(L)3 (m = 7.108 mg). L= benzoate. corresponding to these losses or due to physical phenomenon, Table 2. For the lanthanum to dysprosium com- pounds, the first mass loss (range: 130 – 90ºC), associated to endothermic peaks at 120 – 80 ºC, is ascribed to the dehydration, which occurs in a single step. No influence of the atmosphere (CO2 or air) was observed in the dehydration process of these compounds. Once dehydrated, the anhydrous com- pounds are stable up to 350 ºC (La to Sm), 375 ºC (Eu), 385 ºC (Er, Tm) and 400 ºC (Gd to Ho, Yb, Lu, Y), showing that the anhydrous com- pounds are more stable in CO2 than in an air atmosphere. Above these temperatures the TG – DTA curves show mass losses in steps charac- teristic of each compound and the general aspect of these curves allows the division into the four groups; first group: La, Pr, Nd; second group: Ce, Sm, Gd, Tb; Third group: Eu and fourth group: Dy to Lu and Y. Thus the feature of each of these compounds are discussed on the base of their similar thermal profiles. Lanthanum, praseodymium and neodymium com- pounds The TG-DTA curves of the lanthanum and praseodymium as representative of these com- pounds are shown in Fig. 1. The first mass loss up to 130 ºC (La) and 120 ºC (Pr, Nd) with the cor- responding endothermic peaks at 120 ºC (La) and 110 ºC (Pr, Nd) is due to the release of 2.5H2O (Nd) and 2H2O (La, Pr). After their dehydration the anhydrous compounds are stable up to 350 ºC, and the endothermic peaks at 250 ºC (La), 245 ºC (Pr) and 240 ºC (Nd) are atributed to the reversible crystalline phase transition, in agreement with the thermal decomposition of these compounds in an air atmosphere [25]. The thermal decomposition of the anhy- drous compounds occurs in three (La, Pr) and four (Nd) steps. The first one corresponding to endothermic peaks is attributed to thermal decom- position of these compounds and tests with hydrochloric acid solution on samples heated up to the final temperature of this step, showed in all 45Ecl. Quím., São Paulo, 33(1): 43-48, 2008 cases, the presence of carbonaceous residue and evolution of CO2, indicating the formation of car- bonate or a derivative of carbonate, as intermedi- ate. The formation of carbonate or derivative car- bonate and carbonaceous residue, undoubtedly was favoured by CO2 used as purge gas. The for- 46 Ecl. Quím., São Paulo, 33(1): 43-48, 2008 mation of intermediate derivative of carbonate had already been observed during the thermal decom- position of other lanthanide compounds [26, 27]. The second step corresponding to endother- mic peaks is attributed to the thermal decomposi- tion of the intermediate and carbonaceous residue to lanthanide dioxycarbonate [26, 27]. The last (La, Pr) or the two last (Nd) steps corresponding to endothermic peaks are attributed to the thermal decomposition of the dioxycarbonate to the respec- tive oxide, La2O3, Pr6O11, Nd2O3. Cerium, samarium, gadolinium and terbium com- pounds The TG-DTA curves of the cerium and gadolinium as representative of these compounds are shown in Fig. 1. The first mass loss up to 120 ºC (Ce), 110 ºC(Sm), 105 ºC (Gd) and 95 ºC (Tb) with the corresponding endothermic peak at 115 ºC (Ce), 105 ºC (Sm), 100 ºC (Gd) and 90 ºC (Tb) is due to the dehydration with loss of 2H2O (Ce, Sm), 1.5H2O (Gd) and 1H2O (Tb). The anhydrous compounds are stable up to 350 ºC (Ce, Sm) and 400 ºC (Gd, Tb) and the endothermic peak at 250 ºC (Ce, Gd), 230 ºC (Sm) and 265 ºC (Tb) is ascribed to the reversible crys- talline phase transition, as already observed [25]. The thermal decomposition of the anhy- drous compounds takes place in two steps. The first one accompanied by a small endothermic peak is attributed to the thermal decomposition of these compounds with the formation of a mixture of carbonaceous residue and carbonate or a deriv- ative of carbonate, as intermediate. The last mass loss corresponding to the endothermic peaks is attributed to the thermal decomposition of the carbonaceous residue and of the intermediate to the respective oxide; CeO2, Sm2O3, Gd2O3 and Tb4O7. Europium compound The TG-DTA curves of the europium compound are shown in Fig. 1. The first mass loss up to 110 ºC with the corresponding endothermic peak at 105 ºC is due to the dehy- dration with loss of 1.5H2O. The anhydrous compound is stable up to 375 ºC and the endothermic peak at 245 ºC is attributed to the reversible crystalline phase transition [25]. The thermal decomposition of the anhy- drous compounds takes place in three steps with the two last overlapping ones. The first step correspon- ding to endothermic peak is attributed to the ther- mal decomposition of the compound with the for- mation of a mixture of carbonaceous residue and a derivative of carbonate, as intermediate. The two last overlapping mass losses cor- responding to the endothermic peaks are attrib- uted to the thermal decomposition of the car- bonaceous residue and of the intermediate to the respective oxide, Eu2O3. Dysprosium to lutetium and yttrium compounds The TG-DTA curves of the holmium and ytterbium as representative of these compounds are shown in Fig. 1. these curves show that all the compounds were obtained in the anhydrous state and stable up to 385 ºC (Eu, Tm) 400 ºC (Dy, Ho, Yb, Lu) and 420 ºC (Y) and the endothermic peak at 270 ºC (Dy), 275 ºC (Lu) and 280 ºC (Ho, to Yb, Y) is ascribed to the reversible crystalline phase transition [25]. The thermal decomposition of these compounds occurs in three (Ho to Lu) or four (Dy, Y) steps. The first one corresponding to endothermic peaks is attributed to the thermal decomposition of these compounds with the for- mation of an intermediate derivative of carbonate and carbonaceous residue. Above 620 ºC (Dy to Yb) and 630 ºC (Lu, Y) the mass losses corre- sponding to endothermic peaks are attributed to the thermal decomposition of the intermediate derivative of carbonate followed by the carbona- ceous residue, with formation of the respective oxide, Ln2O3 (Ln= Dy to Lu, Y). For these com- pounds the thermal decomposition of the inter- mediate derivative of carbonate occurs before of the carbonaceous residue, due to the decreasing thermal stability of these intermediates with increasing atomic number of the lanthanide ions, as had already been observed [28]. For this rea- son the large endothermic event between 850 – 1100 ºC attributed to the thermal decomposition of the carbonaceous residue is not observed for the light lanthanide compounds since the car- bonaceous residue is evolved before the thermal decomposition of the intermediate derivative of the carbonate. 47Ecl. Quím., São Paulo, 33(1): 43-48, 2008 References [1]. S. J. Yun, S. K. Kang, S. S.Yun. Thermochim. 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[25]. J. R. Locatelli, E. C. Rodrigues, A. B. Siqueira, E. Y. Ionashiro, G. Bannach, M. Ionashiro J. Thermal Anal. Cal., 90(3) (2007) 737. [26]. L. C. S. de Oliveira, C. B. Melios, M. Spirandeli Crespi, C. A. Ribeiro, M. Ionashiro, Thermochim Acta, 219 (1993) 215. [27]. M. H. Miyano, C. B. Melios, C. A. Ribeiro, H. Redigo, M. Ionashiro, Thermochim. Acta, 221 (1993)53. [28]. L. Moscardini D’ Assunção, I. Giolito, M. Ionashiro, Thermohim. Acta, 137 (1989) 319. Conclusions In the dehydration process of these com- pounds, no influence of the atmosphere (CO2 or air) is observed in TG-DTA curves, however the thermal decomposition of the anhydrous com- pounds significative differences is observed. The thermal decomposition in air atmos- phere, the TG-DTA curves suggest the formation of dioxycarbonate or a mixture of dioxycarbonate and oxide only for La, Nd, Sm and Eu com- pounds, while in a CO2 atmosphere the TG-DTA curves suggest for all the compounds the forma- tion of a mixture of carbonate, oxy or dioxycar- bonate, as intermediate. These curves also show that the thermal stability of the anhydrous compounds is greater in CO2 than in an air atmosphere. Acknowledgements The authors thank FAPESP, CNPq and CAPES Foundations (Brazil) for financial support. Recebido em 30 de janeiro de 2008 Aceito em 04 de março de 2008. 48 Ecl. Quím., São Paulo, 33(1): 43-48, 2008 J. R. Locatelli, A. B. Siqueira , C. T. Carvalho, M. Ionashiro. Decomposição térmica dos ben- zoatos de lantanídeos e ítrio no estado sólido em atmosfera de CO2. Resumo: Foram sintetizados no estado sólido os compostos Ln-Bz, onde Ln representa lantanídeos trivalentes e Bz benzoato. Análise termogravimétrica e análise térmica diferencial (TG/DTA) foi usada para estudar a decomposição térmica destes compostos em atmosfera de CO2. Palavras chaves: lantanídeos, benzoato, decomposição térmica, atmosfera de CO2.