The collisional &activation ot COz(OOO 1) by n-prtrpyl am1 rso-propyl :11c01101 hnr been wdied using the lw~ evctted fhoresccncc method in the tcmpCratUrc range 303-514 K. The cncrgy transfer cros wctl0n5 dccrcascd wltlr increa4inp temperature and near-reson&lnt V-V energy trnnsfcr procclsses 9r(: t
Vibrational deactivation of CO2(0001) by ethane
β Scribed by I.Veerabhadra Rao; Y.V.Chalapati Rao; S.V. Babu; V.Subba Rao
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 403 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
β¦ Synopsis
The deactivation of C&(OO"l) by ethane in.ihe temperature ran9 300-600 K has been strrdied using 2 laser induced fluorescence technique. Thhd energ transfer cross section dccrased from 0.23 A2 at 3CO K to 0.16 AZ at 600 K. The magnitude of the cross section is consistent with the expectation that ncx tCSOMIlt V-V energy transfcr processes are responsible for the energ tnqsfer between COz(OO" L) and cthane during coUisions even thOu$ the observed temperature dependence of the enera transfer cross section does not follow that predicted by the CXisting theories.
π SIMILAR VOLUMES
Intramolecular vibration-vibration energy transfer cross sections have beer. calculated for COz (0001) + H2,!Dz -+ COz(ll'0) + Hz/Dz,+ C02(10Β°0) + Hz/D\*, and-C02(20Β°0) + Hz/D2 based on the mechanism that the energy mismatch is transferred to the translational motion. For CO2 + Hz. the calculated cr
intramoleculv vibration--vibration energy transfer cross sections ha--e been calculated for COs(OO" 1) -I-Ne and COa(OO" 1) + COa (OOOO) over the tempemture range 100-3000 K. It is shown that (00'1) + (11'0) is the most important process at lower temperatures, while (00'1) + (10'0) dominates others