scholarly journals Molecular Vibrational States in the Binary Cold Fission of 252Cf

1997 ◽  
Vol 12 (18) ◽  
pp. 1343-1348 ◽  
Author(s):  
Ş. Mişicu ◽  
A. Săndulescu ◽  
W. Greiner

We predict a molecular vibrational state in the cold binary fission of 252 Cf using a simple decay cluster model. The Hamiltonian of two even–even fragments in the pole–pole configuration is built in the same fashion as that for the dinuclear molecule formed in heavy-ions collisions. The interaction between the two fragments is described by the double-folding M3Y potential. The spectrum of the butterfly vibrations is derived and its dependence on fragments deformation and mass-asymmetry is discussed. Some experimental implications are commented.

2001 ◽  
Vol 691 (3-4) ◽  
pp. 671-690 ◽  
Author(s):  
M. El-Azab Farid ◽  
Z.M.M. Mahmoud ◽  
G.S. Hassan

1996 ◽  
Vol 51 (3) ◽  
pp. 207-214
Author(s):  
Jürgen Preusser ◽  
Manfred Winnewisser

The direct I- type transitions of H133C14N16O in the vibrational states (υ4,υ5) = (01) and (03) were measured in the frequency range from 18 to 40 GHz. These transitions show a nuclear quadrupole hyperfine structure caused by the 14N nucleus, which could partially be resolved at Doppler-limited resolution. The analogous transitions of the parent species. H12C14N16O, were remeasured. They displayed a very similar hyperfine structure, also partially resolved. The hyperfine patterns of both H12C14N16O and H13C14N16O were analysed by means of contour fitting s to the absorption profiles. The parameter ηseQq, which is responsible for the splittings, is determined to be 645(20) kHz for the vibrational state (01) and 890(44) kHz for the vibrational state (03) for H12C14N16O and 642(32) kHz for (01) and 898(22) kHz for (03) for H13C14N16O. This unexpectedly large splitting parameter for states involving the large amplitude motion υ5 (HCN bending) is discussed as another consequence of the quasilinearity of fulminic acid, in view of the fact that the analogous transitions for the vibrational state (10) (NCO bending) do not split or even show a significant line broadening at the resolution used for the present measurements


2018 ◽  
Vol 98 (4) ◽  
Author(s):  
B. D. C. Kimene Kaya ◽  
S. M. Wyngaardt ◽  
T. T. Ibrahim ◽  
W. A. Yahya

1990 ◽  
Vol 05 (26) ◽  
pp. 2101-2105 ◽  
Author(s):  
D. N. POENARU ◽  
M. MIREA ◽  
W. GREINER ◽  
I. CĂTA ◽  
D. MAZILU

A two-center parametrization with smoothed neck is used to describe the shapes during the fission process of 234 U in a wide range of mass asymmetry (cold fission with 100 Zr fragment, 28 Mg radioactivity and α-decay). The optimum fission path has been found by minimizing the action integral. The neck influence is stronger for lower mass asymmetry.


1974 ◽  
Vol 29 (8) ◽  
pp. 1213-1215 ◽  
Author(s):  
N. W. Larsen ◽  
B. P. Winnewisser

Rotational transitions of 16012C32S and 16013C32S in the ground vibrational state and of 16012C32S in several excited states have been accurately measured in the millimeter wave region for a minimum of four different J values. The analysis of the measured frequencies leads to rotational constants for the following vibrational states: 0 00 0 of 16O13C32S and 0 00 0, 0 1 1c 0, 0 1 1d 0, 0 20 0, 0 22c 0, 0 22d 0, 0 00 1 of 16O12C32S. Since the two components of the 0 22 0 transitions were resolved, an analysis of the l-type resonance was carried out and the interval 0 22 0 - 0 20 0 has been determined to be -4.63(10) cm-1. The result is in good agreement with the presently available determination of this level from vibrational spectra.


One object of this series of papers (Lennard-Jones and others 1935-7) is to consider in detail the mechanism of condensation, migration and evaporation of atoms and molecules at solid surfaces and to try to find the processes which govern the transition from one state to another. It has been shown that under certain conditions the thermal vibrations of a solid may activate an adsorbed atom from one vibrational state to a higher one or even eject it from the surface altogether. But the theory there developed is limited in the sense that it deals only with the transfer of single quanta to or from the solid, and consequently the quantized vibrational levels of the adsorbed atom must be closer together than the largest single quantum of energy which the solid can emit. An attempt has been made (Strachan 1937) to find the probability of the simultaneous emission or absorption of several quanta by the solid, and the indication is that the probability of several such simultaneous events is small. Now when atoms are bound to solid surfaces by valency forces, the vibrational levels are widely spaced compared with those of the solid, and many thermal quanta must be transferred simultaneously to the adsorbed atom to change its state of vibration. While this process may occur in nature, it seemed desirable to look for other possible processes whereby adsorbed atoms could be activated to higher vibrational states. One such possible mechanism, in metals at any rate, is by the transfer of energy from the conduction electrons. A simple calculation by classical methods indicates that in a typical case a surface atom may suffer as many as 10 15 collisions per second with the “free” electrons of a metal, and as, according to modern views, these electrons are moving with an energy of several volts, there is here an ample reservoir of energy from which adsorbed atoms may absorb energy or to which they can re-emit it, and thus change their vibrational state, or indeed, also their electronic state.


2005 ◽  
Vol 19 (15n17) ◽  
pp. 2365-2368 ◽  
Author(s):  
CHANG XU ◽  
ZHONGZHOU REN

A new cluster model of α decay is proposed where the effective potential between α-cluster and daughter nucleus is obtained from the double folding integral of the renormalized M3Y nucleon-nucleon interaction and of the density distributions of α particle and daughter nucleus. Without introducing any extra adjustment on the potential, the new model (named as the density-dependent cluster model) can successfully reproduce the experimental half-lives of α decay within a factor of 3. The model also works well for new superheavy elements which are the current interests of nuclear physics and chemistry.


In a previous paper entitled “Structure in the Secondary Hydrogen Spectrum,” Part IV, it was shown that there were a number of bands associated with Fulcher’s bands. It now appears that these and other related bands form a set of band systems whose null lines are connected by a Rydberg-Ritz formula. This formula has the normal value of the Rydberg constant, as is the case with the formula found by Fowler to connect the heads of some of the helium bands. This discovery makes it possible to apportion the effects observed as between electron jumps and vibration jumps, a matter which had to be left open in the previous paper (p. 740). The present paper deals only with the Q branches which are the most strongly developed and have been investigated most fully. A preliminary account of some of the results has been published a letter to ‘Nature,’ but the numbering of the vibrational states of the H α bands proposed therein has since been abandoned. It will be shown that all the lines of Fulcher’s red bands arise as a result of transitions in which the total quantum number (electron jump) changes from 3 to 2 and the vibrational quantum number is unchanged. In the part of the band denoted by A in “Structure,” Part IV, the vibrational state has the lowest possible quantum number both before and after the transition. I shall indicate this state of affairs by the symbol 0 → 0. The corresponding vibrational states in the parts denoted by B, C, D, E and F are, both initially and finally, 1, 2, 3, 4 and 5, and I shall denote these transitions by 1 →1, 2 → 2 , 3 → 3 , 4 → 4 and 5 → 5 respectively. The different lines in part A all have the same electron jump (3 → 2) and the same vibration state (0 → 0) but have different rotational jumps either of the molecule as a whole or of the emitting electron or of both. This statement will be equally true if the letter A is replaced by any of the letters B, C, D, E or F, except that the vibrational jump 0 0 is replaced by 1 → 1, 2 → 2, etc. In the present paper I shall confine my attention to the Q branches so that all the rotational transitions here dealt with are of the type m + ½ → m + ½ , m = 1, 2, 3, 4, 5, etc. (see Part IV, p. 749). Fulcher’s green bands also have the same electron jumps (3 → 2), but in these bands the vibrational quantum number is higher by unity in the initial than in the final states. Thus for the various green bands denoted by the letters A, B, C, D, E and F the vibrational transitions are 1 → 0, 2 → 1, 3 → 2, 4 → 3, 5 → 4 and 6 → 5 respectively. In addition to these, bands with the same electron jump (3 → 2) can be found in the infra-red with the vibrational jumps 0 → 1, 1 → 2, 2 → 3, 3 → 4 and 4 → 5 and others on the side of the green towards the violet which correspond to the vibration jumps 2 → 0, 3 → 1, 4 → 2, 5 → 3 and 6 → 4, and a few lines which may correspond to the vibration jumps 3 → 0 and 5 → 2. All these lines have the electron jump 3 → 2 and are the band analogue of the single line H α in the line spectrum of the hydrogen atom. For this reason it is convenient to refer to this system of bands as the H α bands.


2015 ◽  
Vol 590 ◽  
pp. 012046
Author(s):  
Azni Abdul Aziz ◽  
Norhasliza Yusof ◽  
Muhammad Zamrun Firihu ◽  
Hasan Abu Kassim

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