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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Parmar, ML | - |
| dc.contributor.author | Rao, Ch V Nageshwara | - |
| dc.date.accessioned | 2019-03-25T09:01:55Z | - |
| dc.date.available | 2019-03-25T09:01:55Z | - |
| dc.date.issued | 1990-10 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/46517 | - |
| dc.description | 958-962 | en_US |
| dc.description.abstract | Partial molar volumes and viscosities of ammonium aluminium sulphate and potassium aluminium sulphate have been determined in dimethyl sulphoxide (DMSO) + water (5, 10, 15 and 20 wt %) mixtures at different concentrations and temperatures. The density data have been analysed using Masson's equation. The limiting apparent molar volumes (ϕ ) and the slopes (S ) have been interpreted in terms of solute-solvent and solute-solute interactions, respectively. The ϕ values vary with temperature as a power series of temperature. Structure making/breaking capacities of the multi-charged electrolytes have been inferred from the sign of (∂2ϕ /∂ T2). Both multi-charged electrolytes behave like the symmetrical tetraalkylammonium salts and act as structure makers/promotors. The experimental results of viscosity have been analysed using the Jones-Dole equation. The activation parameters of viscous flow have been obtained to throw light on the mechanism of viscous flow. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.29A(10) [October 1990] | en_US |
| dc.title | Partial molar volumes and viscosities of some multicharged electrolytes in dimethyl sulphoxide-water mixtures | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.29A(10) [October 1990] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 29A(10) 958-962.pdf | 4.74 MB | Adobe PDF | View/Open |
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) and the slopes (S
) have been interpreted in terms of solute-solvent and solute-solute interactions, respectively. The ϕ