Contribution of alpha-cluster transfer processes in 12C(9Be,8Be)13C reactions

1978 ◽  
Author(s):  
L. Jarczyk ◽  
B. Kamys ◽  
A. Strzal̸kowski ◽  
M. Hugi ◽  
J. Lang ◽  
...  
2021 ◽  
Vol 252 ◽  
pp. 04006
Author(s):  
A. Pakou ◽  
P. D. O’Malley ◽  
L. Acosta ◽  
A. M. Sánchez-Benítez ◽  
J. J. Kolata ◽  
...  

Unexpected and challenging experimental results, at below barrier energies for weakly bound nuclei, are briefly reviewed in this article. The emphasis will be on our recent breakup results for 8B+208Pb at deep sub-barrier energies, indicating a dominance of direct mechanisms at this low energy regime. We will also present, a preliminary analysis of the 4He and 3He - particle production events for the 7Be + 208Pb reaction. These data were collected at the same experiment and at similar deep sub-barrier energies, exhibiting large yields compatible with cluster transfer processes. To confirm these results a new experiment to be performed at TriSol is planned, as soon as the upgrading of this facility will be completed.


1980 ◽  
Vol 343 ◽  
pp. 161-188 ◽  
Author(s):  
J. Jänecke ◽  
F.D. Becchetti ◽  
D. Overway

2011 ◽  
Vol 859 (1) ◽  
pp. 29-38 ◽  
Author(s):  
Sh. Hamada ◽  
N. Burtebayev ◽  
K.A. Gridnev ◽  
N. Amangeldi

Author(s):  
M. Arif Hayat

Although it is recognized that niacin (pyridine-3-carboxylic acid), incorporated as the amide in nicotinamide adenine dinucleotide (NAD) or in nicotinamide adenine dinucleotide phosphate (NADP), is a cofactor in hydrogen transfer in numerous enzyme reactions in all organisms studied, virtually no information is available on the effect of this vitamin on a cell at the submicroscopic level. Since mitochondria act as sites for many hydrogen transfer processes, the possible response of mitochondria to niacin treatment is, therefore, of critical interest.Onion bulbs were placed on vials filled with double distilled water in the dark at 25°C. After two days the bulbs and newly developed root system were transferred to vials containing 0.1% niacin. Root tips were collected at ¼, ½, 1, 2, 4, and 8 hr. intervals after treatment. The tissues were fixed in glutaraldehyde-OsO4 as well as in 2% KMnO4 according to standard procedures. In both cases, the tissues were dehydrated in an acetone series and embedded in Reynolds' lead citrate for 3-10 minutes.


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