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dc.contributor.authorManoj, S V-
dc.contributor.authorSingh, R-
dc.contributor.authorSharma, M-
dc.contributor.authorGupta, K S-
dc.date.accessioned2013-09-13T12:52:28Z-
dc.date.available2013-09-13T12:52:28Z-
dc.date.issued2000-05-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21113-
dc.description507-521en_US
dc.description.abstractCadmium sulphide and Mn(II) catalysed autoxidation of aqueous sulphur(IV) has been studied in detail. The CdS catalysed reaction obeys rate law (i), with k3 = 1.17×10-12 mol L-1s-1

-d [S(IV)] /dt = k3 [S(IV)]2 [H+]-2 + k4 [CdS] [S(IV)]2 [H+]-1                              .....(i)

  and k4 = 4.5 × 10-7 L2.mol-2 g-1 s-1 at 30°C in acetate buffered medium. For manganese(II) catalysed reaction, the overall rate law is given by Eq. (ii) with ke =2×10-4 L mol-1s-1 and kf = 6.9×10-2 L2 mol-2 s-1
  Robs = Ro + ke [Mn(II)] [S(IV)] [H+]-1 + kf [Mn(II)] [S(IV)]2 [H+]-1                           ....(ii)

  at 30°C in acetate buffered medium. Ro term represents the uncatalysed and /or trace metal ion catalysed rate. Ethanol strongly inhibits both the reactions indicating the operation of a radical chain mechanism. A study of the effect of ethanol shows that whereas the non-transition metal oxide catalysed sulphur(IV) autoxidation is severely inhibited, the transition metal oxide catalysed autoxidation is inhibited only slightly. This has been interpretated in terms of the operation of a radical chain mechanism in the case of former and a non-radical mechanism in the case of the latter.
en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.39A(05) [May 2000]en_US
dc.titleKinetics and mechanism of heterogeneous cadmium sulphide and homogeneous manganese(II) catalysed oxidation of sulphur(IV) by dioxygen in acetate buffered mediumen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.39A(05) [May 2000]

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