We consider the collinear ternary fission which is a sequential ternary decay with a very short time between the ruptures of two necks connecting the middle cluster of the ternary nuclear system and outer fragments. In particular, we consider the cas
e where the Coulomb field of the first massive fragment separated during the first step of the fission produces a lower pre-scission barrier in the second step of the residual part of the ternary system. In this case, we obtain a probability of about $10^{-3}$ for the yield of massive clusters such as uclide[70]{Ni}, uclide[80-82]{Ge}, uclide[86]{Se}, and uclide[94]{Kr} in the ternary fission of uclide[252]{Cf}. These products appear together with the clusters having mass numbers of $A = 132$--$140$. The results show that the yield of a heavy cluster such as uclide[68-70]{Ni} would be followed by a product of $A = 138$--$148$ with a large probability as observed in the experimental data obtained with the FOBOS spectrometer at the Joint Institute for Nuclear Research. The third product is not observed. The landscape of the potential energy surface shows that the configuration of the Ni + Ca + Sn decay channel is lower about 12 MeV than that of the Ca + Ni + Sn channel. This leads to the fact, that the yield of Ni and Sn is large. The analysis on the dependence of the velocity of the middle fragment on mass numbers of the outer products leads to the conclusion that, in the collinear tripartition channel of uclide[252]{Cf}, the middle cluster has a very small velocity, which does not allow it to be found in experiments.
The evaporation residue yields from compound nuclei $^{220}$Th formed in the $^{16}$O+$^{204}$Pb, $^{40}$Ar+$^{180}$Hf, $^{82}$Se+$^{138}$Ba, $^{124}$Sn+$^{96}$Zr reactions are analyzed to study the entrance channel effects by comparison of the captu
re, fusion and evaporation residue cross sections calculated by the combined dinuclear system (DNS) and advanced statistical models. The difference between evaporation residue (ER) cross sections can be related to the stages of compound nucleus formation or/and at its surviving against fission. The sensitivity of the both stages in the evolution of DNS up to the evaporation residue formation to the angular momentum of DNS is studied. The difference between fusion excitation functions are explained by the hindrance to complete fusion due to the larger intrinsic fusion barrier $B^*_{rm fus}$ for the transformation of the DNS into a compound nucleus and the increase of the quasifission contribution due to the decreasing of quasifission barrier $B_{rm qf}$ as a function of the angular momentum. The largest value of the ER residue yields in the very mass asymmetric $^{16}$O+$^{204}$Pb reaction is related to the large fusion probability and to the relatively low threshold of the excitation energy of the compound nucleus. Due to the large threshold of the excitation energy (35 MeV) of the $^{40}$Ar+$^{180}$Hf reaction, it produces less the ER yields than the almost mass symmetric $^{82}$Se+$^{138}$Ba reaction having the lowest threshold value (12 MeV).
A possibility of formation of the three reaction products having comparable masses at the spontaneous fission of $^{252}$Cf is theoretically explored. This work is aimed to study the mechanism leading to observation of the reaction products with mass
es $M_1=$136---140 and $M_2=$68---72 in coincidence by the FOBOS group in JINR. The same type of ternary fission decay has been observed in the reaction $^{235}$U(n$_{rm th}$,fff). The potential energy surface for the ternary system forming a collinear nuclear chain is calculated for the wide range of mass and charge numbers of constituent nuclei. The results of the PES for the tripartition of $^{252}$Cf(sf,fff) shows, that we have favorable dynamical conditions for the formation of fragments with mass combinations of clusters $^{68-70}$Ni with $^{130-132}$Sn and with missing cluster $^{48-52}$Ca.
The synthesis of superheavy elements stimulates the effort to study the peculiarities of the complete fusion with massive nuclei and to improve theoretical models in order to extract knowledge about reaction mechanism in heavy ion collisions at low e
nergies. We compare the theoretical results of the compound nucleus (CN) formation and evaporation residue (ER) cross sections obtained for the $^{48}$Ca+$^{248}$Cm and $^{58}$Fe+$^{232}$Th reactions leading to the formation of the isotopes A=296 and A=290, respectively, of the new superheavy element Lv (Z=116). The ER cross sections, which can be measured directly, are determined by the complete fusion and survival probabilities of the heated and rotating compound nucleus. That probabilities can not be measured unambiguously but the knowledge about them is important to study the formation mechanism of the observed products. For this aim, the $^{48}$Ca+$^{249}$Cf and $^{64}$Ni+$^{232}$Th reactions have been considered too. The use of the mass values of superheavy nuclei calculated in the framework of the macroscopic-microscopic model by Warsaw group leads to smaller ER cross section for all of the reactions (excluding the $^{64}$Ni+$^{232}$Th reaction) in comparison with the case of using the masses calculated by Peter Moller {it et al}.
The fusion and evaporation residue cross sections for the $^{50}$Ti+$^{249}$Cf and $^{54}$Cr+$^{248}$Cm reactions calculated by the combined dinuclear system and advanced statistical models are compared. These reactions are considered to be used to s
ynthesize the heaviest superheavy element. The $^{50}$Ti+$^{249}$Cf reaction is more mass asymmetric than $^{54}$Cr+$^{248}$Cm and the fusion excitation function for the former reaction is higher than the one for the latter reaction. The evaporation residue excitation functions for the mass asymmetric reaction is higher in comparison with the one of the $^{54}$Cr+$^{248}$Cm reaction. The use of the mass values of superheavy nuclei calculated in the framework of the macroscopic-microscopic model by the Warsaw group leads to smaller evaporation residue cross section for both the reactions in comparison with the case of using the masses calculated by Peter Moller {it et al}. The $^{50}$Ti+$^{249}$Cf reaction is more favorable in comparison with the $^{54}$Cr+$^{248}$Cm reaction: the maximum values of the excitation function of the 3n-channel of the evaporation residue formation for the $^{50}$Ti+$^{249}$Cf and $^{54}$Cr+$^{248}$Cm reactions are about 0.1 and 0.07 pb, respectively, but the yield of the 4n-channel for the former reaction is lower (0.004 pb) in comparison with the one (0.01 pb) for the latter reaction.
The mechanism leading to the formation of the observed products of the collinear cluster tripartition is carried out within the framework of the model based on the dinuclear system concept. The yield of fission products is calculated using the statis
tical model based on the driving potentials for the fissionable system. The minima of potential energy of the decaying system correspond to the charge numbers of the products which are produced with large probabilities in the sequential fission (partial case of the collinear cluster tripartition) of the compound nucleus. The realization of this mechanism supposes the asymmetric fission channel as the first stage of sequential mechanism. It is shown that only the use of the driving potential calculated by the binding energies with the shell correction allows us to explain the yield of the true ternary fission products. The theoretical model is applied to research collinear cluster tripartition in the reaction $^{235}$U(n$_{rm th}$,f). Calculations showed that in the first stage of this fission reaction, the isotopes $^{82}$Ge and $^{154}$Nd are formed with relatively large probabilities and in the second stage of sequential fission of the isotope Nd mainly Ni and Ge are formed. This is in agreement with the yield of the isotope $^{68}$Ni which is observed as the product of the collinear cluster tripartition in the experiment.
A variety of phenomena connected with the formation of a dinuclear complex is observed in the heavy ion collisions at low energies. The dinuclear system model allows us to analyze the experimental data and to interpret them by comparison of the parti
al capture, fusion and evaporation residue cross sections measured for the different reactions leading to the same compound nucleus. The comparison of theoretical and experimental values of the mass and angular distributions of the reaction products gives us a detailed information about reaction mechanism forming the observed yields. The observed very small cross sections of the evaporation residues may be explained by the strong fusion hindrance and/or instability of the heated and rotating compound nucleus and smallness of its survival probability. The fusion hindrance arises due to competition between complete fusion and quasifission while the smallness of survival probability is connected with the decrease of the fission barrier at large excitation energy and angular momentum of compound nucleus.
The excitation functions of capture, complete fusion, and evaporation residue formation in the $^{16}$O+$^{184}$W and $^{19}$F+$^{181}$Ta reactions leading to the same $^{200}$Pb compound nucleus has been studied theoretically to explain the experime
ntal data showing more intense yield of evaporation residue in the former reaction in comparison with that in the latter reaction. The observed difference is explained by large capture cross section in the former and by increase of the quasifission contribution to the yield of fission-like fragments in the $^{19}$F+$^{181}$Ta reaction at large excitation energies. The probability of compound nucleus formation in the $^{16}$O+$^{184}$W reaction is larger but compound nuclei formed in both reactions have similar angular momentum ranges at the same excitation energy. The observed decrease of evaporation residue cross section normalized to the fusion cross section in the $^{19}$F+$^{181}$Ta reaction in comparison with the one in the $^{16}$O+$^{184}$W reaction at high excitation energies is explained by the increase of hindrance in the formation of compound nucleus connected with more quick increase of the quasifission contribution in the $^{19}$F induced reaction. The spin distributions of the evaporation residue cross sections for the two reactions are also presented.
The angular distributions of fission fragments for the $^{32}$S+$^{184}$W reaction at center-of-mass energies of 118.8, 123.1, 127.3, 131.5, 135.8, 141.1 and 144.4 MeV were measured. The experimental fission excitation function is obtained. The fragm
ent angular anisotropy ($mathcal{A}_{rm exp}$) is found by extrapolating the each fission angular distributions. The measured fission cross sections of the $^{32}$S+$^{182,184}$W reaction are decomposed into fusion-fission, quasifission and fast fission contributions by the dinuclear system model. The total evaporation residue excitation function for the $^{32}$S+$^{184}$W reaction calculated in the framework of the advanced statistical model is in good agreement with the available experimental data up to about $E_{rm c.m.}approx 160$ MeV. The theoretical descriptions of the experimental capture excitation functions for both reactions and quantities $K_0^2$, $<ell^2>$ and $mathcal{A}_{rm exp}$ which characterize angular distributions of the fission products were performed by the same partial capture cross sections at the considered range of beam energy.
The effect of ultralow-frequency or static magnetic and electric fields on biological processes is of huge interest for researchers due to the resonant change of the intensity of biochemical reactions although the energy in such fields is small. A si
mplified model to study the effect of the weak magnetic and electrical fields on fluctuation of the random ionic currents in blood and to solve the $k_BT$ problem in magnetobiology is suggested. The analytic expression for the kinetic energy of the molecules dissolved in certain liquid media is obtained. The values of the magnetic field leading to resonant effects in capillaries are estimated. The numerical estimates showed that the resonant values of the energy of molecular in the capillaries and aorta are different: under identical conditions a molecule of the aorta gets $10^{-9}$ times less energy than the molecules in blood capillaries. So the capillaries are very sensitive to the resonant effect, with an approach to the resonant value of the magnetic field strength, the average energy of the molecule localized in the capillary is increased by several orders of magnitude as compared to its thermal energy, this value of the energy is sufficient for the deterioration of the chemical bonds.
