Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/26063Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pachauri, Manisha | - |
| dc.contributor.author | Upadhyay, Santosh K | - |
| dc.date.accessioned | 2014-01-24T09:47:29Z | - |
| dc.date.available | 2014-01-24T09:47:29Z | - |
| dc.date.issued | 2000-07 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/26063 | - |
| dc.description | 747-750 | en_US |
| dc.description.abstract | Polymerization of methyl methacrylate (MMA) with triethanolamine (TEA) and carbon tetrachloride has been investigated in the presence of RuCl3 and in dimethyl sulphoxide (DMSO) medium by employing a dilatometric technique at 60oC. The rate of polymerization (Rp) of MMA has been found to be proportional to [MMA], [TEA]1/2 [CCl4]1/2 and {kI+ kII[RuCL3]1/2} where kI and kII are rate constants for uncatalysed and catalysed polymerization respectively. The rate of polymerization has been inhibited by hydroquinone, suggesting a free radical mechanism. The kinetic data indicate the possible participation of the charge transfer complex formed between {TEA-RuIII} and CCl4 during the polymerization of MMA. In the absence of either TEA or CCl4, no polymerization of MMA has been observed under the present experimental conditions. | 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.39A(07) [July 2000] | en_US |
| dc.title | Kinetics of ruthenium (III) catalysed polymerization of methyl methacrylate by triethanolamine in presence of CCl4 | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.39A(07) [July 2000] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 39A(7) 747-750.pdf | 3.33 MB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.