The knowledge of the physicochemical properties of the basic lead sulphates is of great interest from the point of view of the technology of lead-acid batteries.Facultad de Ciencias Exacta

Baran, Enrique José

Grasselli, M. C.

Journal of Materials Science Letters

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J O U R N A L  O F  M A T E R I A L S  S C I E N C E  L E T T E R S  3 ( 1 9 8 4 )  9 4 9 - 9 5 0  IR spectroscopic characterization of tetrabasic lead sulphate M.C.  GRASSELL I ,  E. J. BARAN Area de Oufmica Inorg~nica, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, 1900-La Plata, Argentina The knowledge of the physicochemical properties of the basic lead sulphates is of great interest from the point of view of the technology of lead-acid batteries. Crystallographic data for the tetrabasic lead sulphate, PbSOg.4PbO, have recently been repor- ted [1] and as it is also possible to obtain this phase in a very pure form [1, 2], we have investi- gated its infrared (IR) spectrum in order to obtain an insight into the spectroscopic behaviour of such materials and also to facilitate their identi- fication by this method. Pure samples of PbSO4.4PbO have been obtained in the form of microcrystalline powders, by the reaction of PbO with diluted HzSO4 (spe- cific gravity = 1.4g cm -3) at 80°C during 4 to 6h  and subsequent heating of the product at 550°C [2]. The samples were characterized by their pow- der diagram [1 ]. The IR spectra were recorded with a Perkin Elmer 580 B-spectrophotometer using the KBr pellet technique. The spectrum of one of the pre- pared PbSOa'4PbO samples is shown in Fig. 1. As PbSO4"4PbO belongs to the monoclinic sys- tem, space group P21/c and Z = 4, the ideally tetrahedral SO~- ions are located in the crystal on the general Ca positions. Therefore, according to a site symmetry analysis [3, 4], a total activation and a complete removement of degeneracies of the vibrational modes of the tetrahedral ion are expec- ted. These predictions are fully confirmed both in the stretching and bending regions of the sulphate vibrations. The antisymmetric stretching vibration u3 appears to be split into four components, located at 1051, 1077, 1105 and 1135 cm -x. The fact that there is one band more than those predicted by the site symmetry analysis can be explained by the activation of a combination mode or by the con- tribution of dynamic crystal field effects, which originate in the interaction between the anions in the unit cell. 0261-8028/84 $03.00 +.  12 The symmetric stretching vibration vt, which is also activated in the crystal, is clearly seen as a sharp band at 965 cm -1. In the bending region, the antisymmetric defor- mation mode u4 appears as a well defined doublet at 609 to 600 cm -1, whereas the third expected component can be seen as a weak shoulder at 614cm -1. The symmetric bending vibration v2, which usually lies around 450cm -1 [3] is over- lapped by the strong band multiplet lying below 500 cm -1 (peaks at 483,445 (sh), 430 (sh), 372, 341 (sh), 290 and 278(sh)cm-X). This last multi- plet is surely associated with PbO modes, as has been shown in our former study of the phases V2Os'4PbO and V2Os-8PbO, which present strong absorptions in the same spectral range [5]. Pure PbO also possesses strong bands in this region [6]. Comparison of the PbSO4"4PbO spectrum and that of pure PbSO4 [7] shows a slight displacement of all bands to lower wave numbers in the case of the basic sulphate. As it has been shown by Dapo [2], basic lead sulphates always retain some amount of carbon dioxide and water. He postulates that, in general, the composition of tetrabasic lead sulphate may be formulated as (PbSO4)I_x(PbCO3"H20)x'4PbO. The CO2 and H20 can be eliminated by the heating process at 550 ° C [2]. 1200 1000 800 I I I I 600 400 (cm_~) Figure 1 Infrared spectrum of PbSO4.4PbO. © 1984 Chapman and Hail Ltd. 949 IR spectra of samples not subjected to the heat treatment are slightly more diffuse than those of pure PbSO4"4PbO. The sulphate bands appear at 1132, 1095, 1040, 962 and 610/601 cm -1, i.e. slightly displaced in relation to those of the pure material. The disappearance of one of the v3 com- ponents in the carbonated samples, strongly sup- ports the idea that the origin of the fourth band in this region, in the case of pure PbSO4-4PbO, must be a dynamic coupling effect. As the CO~- ions occupy a part of the SO~- positions in the lattice, they cause a diminution of the SO4/SO 4 interac- tions and partially suppress this coupling effect. The spectrum also shows two of the carbonate bands (1400cm -~, strong and broad; 685 cm -1, medium and well defined), whereas the water bands are very weak and not clearly defined. Finally, it is very interesting to comment that when pure PbSO4"4PbO samples are maintained for some weeks in direct contact with air, they absorb newly atmospheric CO2, which is easily detected by the appearance of the two character- istic carbonate absorption bands. But the incor- porated CO2 can be eliminated by a short reheating of the sample at 550 ° C. This study has also shown that the spectro- scopic behaviour of tetrabasic lead sulphate is in good agreement with the theoretical expectations based on a site symmetry analysis. The IR spec- trum, which is very characteristic and repro- ducible, shows two typical regions, one dominated by the internal SO~- vibrations (1200 to 600cm -1) and the other by PbO modes (550 to 250 cm-1). Also, carbonate impurities, which can usually be present in these materials, are easily detected by their strong IR absorptions at 1400 and 685 cm -1. Acknowledgements This work was supported by CONICET (Programa "QUINOR") and CICPBA. MCG acknowledges also a special support from the CRUN, which made possible her participation in this research. References 1. B. F. MENTZEN, J. C. VIALA, A. SARTRE and J. BOUIX, Compt. Rend. Acad. Sci. Paris Sdr. H 293 (1981) 1053. 2. R. F. DAPO, J. Eleetrochem. Soc. 121 (1974) 253. 3. S. D. ROSS, "Inorganic Infrared and Raman Spectra" (McGraw Hill, London, 1972), 4. A. MULLER, E.J. BARAN and R.O. CARTER, Struet. Bonding 26 (1976) 81. 5. M.E. ESCOBAR and E. J. BARAN, Z. Anorg. Allg. Chem. 453 (1979) 190. 6. J. D. DONALDSON, M.T. DONOGHUE and S.D. ROSS, Spectrochim. Acta 30A (1974) 1967. 7. E. STEGER and W. SCHMIDT, Bet. Bunsenges. Phys. Chem. 68 (1964) 102. Received 6 March and accepted 26 March 1984 950 

IR spectroscopic characterization of tetrabasic lead sulphate

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IR spectroscopic characterization of tetrabasic lead sulphate

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