Attack of YBa2Cu3O6.8 by acidic aqueous solutions

The dissolution of YBa2Cu3O6.8 in acidic aqueous solutions was studied at 298 K as a function of pH, nature and concentration of present anions and time, t. In the range 2.0 ≤ pH ≤ 4.0, dissolution is congruent and proceeds to completion; dissolution profiles are deceleratory and comply with a contr...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autor principal: Candal, R.J
Otros Autores: Blesa, M.A, Regazzoni, A.E
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Springer Netherlands 1996
Materias:
PH
Acceso en línea:Registro en Scopus
DOI
Handle
Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
LEADER 07916caa a22009977a 4500
001 PAPER-3422
003 AR-BaUEN
005 20230518203253.0
008 190411s1996 xx ||||fo|||| 00| 0 eng|d
024 7 |2 scopus  |a 2-s2.0-0029732084 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JMTSA 
100 1 |a Candal, R.J. 
245 1 0 |a Attack of YBa2Cu3O6.8 by acidic aqueous solutions 
260 |b Springer Netherlands  |c 1996 
270 1 0 |m Candal, R.J.; INQUIMAE, Facultad de Ciencias Exactes, Pabellón 2, 1428-Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Myhra, S., Pham, D.K., Smart, R.St.C., Turner, P.S., (1991) Science of Ceramic Interfaces, p. 569. , edited by J. Nowotny Elsevier, Amsterdam 
504 |a Barkatt, A., Hojaji, H., Amarakoon, V.R.W., Fagan, J.G., (1993) Mater. Res. Soc. Bull., SEPTEMBER, p. 45 
504 |a Hyde, B.G., Thompson, J.G., Withers, R.L., Fitzgerald, J.D., Stewart, A.M., Bevan, D.J.M., Anderson, J.S., Paterson, M.S., (1987) Nature, 327, p. 402 
504 |a Thompson, J.G., Hyde, B.G., Withers, R.L., Anderson, J.S., Fitzgerald, J.D., Bitmead, J., Paterson, M.S., Stewart, A.M., (1987) Mater. Res. Bull., 22, p. 1715 
504 |a Wang, J., Stevens, R., Bultitude, J., (1988) J. Mater. Sci., 23, p. 3393 
504 |a Bansal, N.P., Sandkuhl, A.L., (1988) Appl. Phys. Lett., 52, p. 323 
504 |a Horowitz, H.S., Bordia, R.K., Flippen, R.B., Johnson, R.E., Chowdhry, U., (1988) Mater. Res. Bull., 23, p. 821 
504 |a Jin, S.G., Liu, L.G., Zhu, Z.Z., Huang, Y.L., (1989) Solid State Commun., 69, p. 179 
504 |a Dexin, Z., Mingshan, X., Ziqing, Z., Shubin, Y., Huansui, Z., Shuxia, S., (1988) Solid State Commun., 65, p. 339 
504 |a Dominec, J., Smrčka, L., Vašek, P., Geurten, S., Smrčková, O., Sýkorová, D., Hájek, B., (1988) Solid State Commun., 65, p. 373 
504 |a Pham, D.K., Rupeng, Z., Fielding, P.E., Myhra, S., Turner, P.S., (1991) J. Mater. Res., 6, p. 1148 
504 |a Rupeng, Z., Goringe, M.J., Myhra, S., Turner, P.S., (1992) Phil. Mag. A, 66, p. 491 
504 |a Zhou, J.P., Riley, D.R., McDevitt, J.T., (1993) Chem. Mater., 5, p. 361 
504 |a McDevitt, J.T., Longmire, M., Gollmar, R., Jernigan, J.C., Dalton, E.F., McCarley, R., Murray, R.W., Collman, J.P., (1988) J. Electroanal. Chem., 243, p. 465 
504 |a Rochani, S., Hibbert, D.B., Dou, S.X., Bourdillon, A.J., Liu, H.K., Zhou, J.P., Sorrell, C.C., (1988) J. Electroanal. Chem., 248, p. 461 
504 |a Rosamilia, J.M., Miller, B., (1988) J. Electroanal. Chem., 249, p. 205 
504 |a Rosamilia, J.M., Miller, B., (1988) J. Electroanal. Soc., 135, p. 3030 
504 |a Rosamilia, J.M., Miller, B., Schneemeyer, L.F., Waszczak, J.V., O'Bryan Jr., H.M., (1987) J. Electroanal. Soc., 134, p. 1863 
504 |a Magee, V.M., Rosamilia, J.M., Kometani, T.K., Schneemeyer, L.F., Waszczak, J.V., Miller, B., (1988) J. Electroanal. Soc., 135, p. 3026 
504 |a Hepburn, B.J., Lau, H.L., Lyon, S.B., Newman, R.C., Thompson, G.E., Alford, N., (1992) Corrosion Sci., 33, p. 515 
504 |a Crubelatti, R., Smichowski, P., Battistoni, D., Polla, G., Manghi, E., (1990) Solid State Commun., 75, p. 101 
504 |a Gautier, E.A., Gettar, R.T., Servant, R.E., (1988) Anal. Chim. Acta, 6, p. 281 
504 |a Urrutia, G.A., Blesa, M.A., (1988) React. Solids, 6, p. 281 
504 |a Blesa, M.A., Morando, P.J., Regazzoni, A.E., (1994) Chemical Dissolution of Metal Oxides, , CRC Press, Boca Raton, FL 
504 |a Myhra, S., Smart, R.St.C., Turner, P.S., (1988) Scanning Microsc., 2, p. 715 
504 |a Stumm, W., Holh, H., Dalang, F., (1976) Croat. Chem. Acta, 48, p. 491 
504 |a Schindler, P.W., Stumm, W., (1987) Aquatic Surface Chemistry, , edited by W. Stumm Wiley, New York, Ch. 4 
504 |a Wieland, E., Wehrli, B., Stumm, W., (1988) Geochim. Cosmochim. Acta, 52, p. 1969 
504 |a Furrer, G., Stumm, W., (1986) Geochim. Cosmochim. Acta, 50, p. 1847 
504 |a Zinder, B., Furrer, G., Stumm, W., (1986) Geochim. Cosmochim. Acta, 50, p. 1861 
504 |a Vermilyea, D.A., (1966) J. Electrochem. Soc., 113, p. 1067 
504 |a Diggle, J.W., (1973) Oxides and Oxide Films, 2. , edited by J. W. Diggle Marcel Dekker, New York, Ch. 4 
504 |a Valverde, N., (1976) Ber. Bunsenges. Phys. Chem., 80, p. 333 
504 |a Shevelev, N.P., Gorichev, J.G., Klyuchnikov, N.G., Nasarova, R.I., (1974) Russian J. Inorg. Chem., 19, p. 931 
504 |a Huheey, J.E., (1978) Inorganic Chemistry: Principles of Structure and Reactivity, , Ch. 12, 2nd Edn Harper & Row, New York 
504 |a Salvador, P., Fernández Sánchez, E., García Domínguez, J.A., Amador, J., Cascales, C., Rasines, I., (1989) Solid State Commun., 70, p. 71 
520 3 |a The dissolution of YBa2Cu3O6.8 in acidic aqueous solutions was studied at 298 K as a function of pH, nature and concentration of present anions and time, t. In the range 2.0 ≤ pH ≤ 4.0, dissolution is congruent and proceeds to completion; dissolution profiles are deceleratory and comply with a contracting volume rate law up to t0.5. The rate of dissolution, which is limited by slow surface reactions, decreases with increasing pH; the kinetic order on proton concentration is a fractional and variable number. At higher pH values, dissolution is arrested at intermediate conversion values. In these cases, congruent dissolution is followed by the precipitation of less soluble solid phases which form a passive layer. The nature of this passive layer depends on pH and on the nature and concentration of present anions, which also define the extent of conversion attained at passivation. The dissolution behaviour of YBa2Cu3O6.8 is described in terms of two consecutive surface reactions: fast equilibrated protonation of surface metal ions is followed by the slow release of cations. Barium surface ions are identified as the more reactive sites. The effect of the fast initial leaching of barium ions on the reactivity of yttrium and copper sites is discussed. The influence of the formal Cu(III) oxidation state is also stressed. © 1996 Chapman & Hall.  |l eng 
593 |a INQUIMAE, Facultad de Ciencias Exactes, Pabellón 2, 1428-Buenos Aires, Argentina 
593 |a Departamento Químíca de Reactores, Comisión Nacional de Energía Atómica, Av. del Libertador 8250, 1429-Buenos Aires, Argentina 
690 1 0 |a BARIUM 
690 1 0 |a CHEMICAL REACTIONS 
690 1 0 |a COPPER 
690 1 0 |a DISSOLUTION 
690 1 0 |a IONS 
690 1 0 |a LEACHING 
690 1 0 |a OXIDATION 
690 1 0 |a PRECIPITATION (CHEMICAL) 
690 1 0 |a PROTONS 
690 1 0 |a SOLUTIONS 
690 1 0 |a SURFACE PHENOMENA 
690 1 0 |a ACIDIC AQUEOUS SOLUTIONS 
690 1 0 |a OXIDATION STATE 
690 1 0 |a PASSIVE LAYER 
690 1 0 |a PROTONATION 
690 1 0 |a SURFACE REACTIONS 
690 1 0 |a VOLUME RATE LAW 
690 1 0 |a YTTRIUM BARIUM COPPER OXIDE 
690 1 0 |a OXIDE SUPERCONDUCTORS 
650 1 7 |2 spines  |a PH 
700 1 |a Blesa, M.A. 
700 1 |a Regazzoni, A.E. 
773 0 |d Springer Netherlands, 1996  |g v. 31  |h pp. 54-60  |k n. 1  |p J Mater Sci  |x 00222461  |w (AR-BaUEN)CENRE-5658  |t Journal of Materials Science 
856 4 1 |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029732084&doi=10.1007%2fBF00355126&partnerID=40&md5=f8634f5fbca7edef50dbbc96051f31be  |y Registro en Scopus 
856 4 0 |u https://doi.org/10.1007/BF00355126  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00222461_v31_n1_p54_Candal  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00222461_v31_n1_p54_Candal  |y Registro en la Biblioteca Digital 
961 |a paper_00222461_v31_n1_p54_Candal  |b paper  |c PE 
962 |a info:eu-repo/semantics/article  |a info:ar-repo/semantics/artículo  |b info:eu-repo/semantics/publishedVersion 
999 |c 64375