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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Routra, N | - |
| dc.contributor.author | Bhatta, D | - |
| dc.date.accessioned | 2013-02-11T17:04:28Z | - |
| dc.date.available | 2013-02-11T17:04:28Z | - |
| dc.date.issued | 1999-10 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/15947 | - |
| dc.description | 1047-1050 | en_US |
| dc.description.abstract | Influence
of the semiconducting
oxide, CuO,
(1.0-10.0 mol%) and -irradiation
(0.5-5.0×102 KGy) on the thermal decomposition of barium
oxalate has been studied by the gas evolution
method. The process
occurs through initial gas evolution followed by a
sigmoidal zone consisting of acceleratory and
decay periods.
Lower concentrations of the additive reduce the value of fraction decomposed, , and decrease the rate of reaction in the acceleratory
and decay
stages, the effect being more
prominent in the case of former. However, reaction
rate
increases with increasing concentration of the additive. The extent
as well as the rate of decomposition in the acceleratory stage is facilitated on irradiation
but the reverse takes place in the decay period, the effect being higher at higher doses. | 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.38A(10) [October 1999] | en_US |
| dc.title | Role of semiconducting oxide (CuO) and -irradiation on the thermal decomposition of barium oxalate | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.38A(10) [October 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 38A(10) 1047-1050.pdf | 792.65 kB | Adobe PDF | View/Open |
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-irradiation
(0.5-5.0×102 KGy) on the thermal decomposition of barium
oxalate has been studied by the gas evolution
method. The process
occurs through initial gas evolution followed by a
sigmoidal zone consisting of acceleratory and
decay periods.
Lower concentrations of the additive reduce the value of fraction decomposed,
, and decrease the rate of reaction in the acceleratory
and decay
stages, the effect being more
prominent in the case of former. However, reaction
rate