New method for calculation of nuclear cluster structure of nuclei

2005 ◽  
Author(s):  
A. I. Ibishi
2021 ◽  
Vol 103 (5) ◽  
Author(s):  
Lei Wang ◽  
Jian Liu ◽  
Rensheng Wang ◽  
Mengjiao Lyu ◽  
Chang Xu ◽  
...  

2013 ◽  
Vol 110 (26) ◽  
Author(s):  
Bo Zhou ◽  
Y. Funaki ◽  
H. Horiuchi ◽  
Zhongzhou Ren ◽  
G. Röpke ◽  
...  

2011 ◽  
Vol 20 (04) ◽  
pp. 938-942 ◽  
Author(s):  
YU. E. PENIONZHKEVICH

Experimental excitation functions are presented for complete fusion and transfer reactions in the interaction of 6 He and 6,8,9 Li with 206 Pb , 209 Bi , and nat Pt targets. The data on fusion in the 6 He -induced reactions at energies close to the Coulomb barrier differ from predictions within the framework of the statistical model for compound nucleus decay. For these exit channels a strong enhancement has been observed. Enhancement of the cross section for neutron transfer (with the 6 He and 8,9 Li beams) and deuteron transfer (with the 6 Li beam) reactions is observed at deep sub-barrier energies. The results are discussed from the viewpoint of how the nuclear cluster structure influences the probability of interaction at near-barrier energies.


Author(s):  
C. C. Clawson ◽  
L. W. Anderson ◽  
R. A. Good

Investigations which require electron microscope examination of a few specific areas of non-homogeneous tissues make random sampling of small blocks an inefficient and unrewarding procedure. Therefore, several investigators have devised methods which allow obtaining sample blocks for electron microscopy from region of tissue previously identified by light microscopy of present here techniques which make possible: 1) sampling tissue for electron microscopy from selected areas previously identified by light microscopy of relatively large pieces of tissue; 2) dehydration and embedding large numbers of individually identified blocks while keeping each one separate; 3) a new method of maintaining specific orientation of blocks during embedding; 4) special light microscopic staining or fluorescent procedures and electron microscopy on immediately adjacent small areas of tissue.


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