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HAL Id: jpa-00214855

https://hal.archives-ouvertes.fr/jpa-00214855

Submitted on 1 Jan 1971

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TRANSFER REACTIONS BETWEEN 18O IONS AND LIGHT NUCLEI

Y. Eyal, I. Dostrovsky, Z. Fraenkel

To cite this version:

Y. Eyal, I. Dostrovsky, Z. Fraenkel. TRANSFER REACTIONS BETWEEN 18O IONS AND LIGHT NUCLEI. Journal de Physique Colloques, 1971, 32 (C6), pp.C6-189-C6-191.

�10.1051/jphyscol:1971637�. �jpa-00214855�

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JOURNAL DE PHYSIQUE Colloque C6, supplkment au no 1 1-1 2, Tome 32, Novembre-De'cembre 197 1, page C6-189

TRANSFER REACTIONS BETWEEN ''0 IONS AND LIGHT NUCLEI

Y. EYAL, I. DOSTROVSKY and Z. FRAENKEL The Weizmann Institute of Science, Rehovot, Israel

R&umk. - Les sections efficaces cx$rimentales des reactions dc transfert de deux neutrons 180(180, 200)160 et 14C(180, 200)IZC sont comparkes aux sections efficaces des reactions de transfert d'un neutron correspondantes. Aux energies incidentes proches de la barriere coulom- bienne, on observe des sections efficaces considerablement plus grandes pour les rkctions de transfert de deux neutrons. Les fonctions d'excitation et les distributions angulaires experimentales de la reaction de transfert de deux neutrons 2Wg(l80, 160)28Mg sont comparees a des calculs faits dans le cadre de I'approximation de Born avec ondes deformks et du modele diffractionnel.

Abstract. -The experimental 180(130, 200)lG0 and 14C(I", 2"0)12C Zneutron transfer reaction cross sections are compared with the corresponding single-neutron transfer reactions.

The 2-neutron transfer reactions are found to have a considerably larger cross section at bombar- ding energies near the Coulon~b barrier. The experimental excitation function and angular distri- bution of the 26Mg(lxO, 160)28Mg 2-neutron transfer reaction are compared to calculations based on the DWBA method and the diffraction model.

In figure 1 we show the excitation functions for the 2-neutron transfer reaction 180("0, 200)160, the single-neutron transfer reaction 180('80, 190)170 and the triton transfer reaction "O("0, I5N)"F.

These reactions were measured by bombarding a thin (75 pg/cmz oxygen) target of highly enriched (98 %

"0) tantalum oxide on 21 mg/cm2 tantalum backing with ''0 ions. The reaction products were stopped in the tantalum backing and the 190, 200 and "F formation cross sections were determined on the basis of the gamma ray energy and half life of these nuclides. In figure 2 we show the experimental excita-

reactions respectively since the alternative possibility (6He and 5He transfer) involves the transfer of much heavier and more strongly bound clusters.

Moreover, the comparison of figures 1 and 2 shows a great similarity of the ("0, "0) and ("0, 190) excitation functions for the two targets. The most important conclusion which may therefore be drawn from the experimental results of figures 1 and 2 is that for both the "0

+

"0 and the ''0

+

14C reaction channels the 2-neutron transfer reactions cross section is considerably larger than the single- tion functions for the reactions 14c(180, 160)16C

.,

; In0 I + I 8

1 4 ~ ( 1 8 0 , 2 0 0 ) 1 2 ~ ; 1 4 ~ ( 1 8 0 , 1 9 0 ) 1 3 ~ and 1 418 ~

( 0 9

15N)17N. These cross sections were determined by

,,-

bombarding a 125 pg/cm2 thick enriched (83 o/,

1 4) 14 ~C-polyacetylene target on 245 mg/cm2 gold backing with ''0 ions. The '4C(180, 2 0 0 ) 1 2 C and

14C(180, 190)13C cross sections were again determined : o - through the measurement of the "0 and "0 gamma

activity whereas the cross sections of the remaining 2 -

two reactions were measured by counting the delayed b neutron activity of the "N and 16C reaction products with a BF,-paraffin neutron counter. Since the detailed decay scheme of '% is unknown we have assumed that one delayed neutron is emitted per

disintegration of 16C. Unlike the case of the "0

+

"0

,,,

reaction the transferred clusters are not uniquely

determined by the reaction products in the "0

+

14C I c 20 25 30 35 . I.- 40

reactions. Yet one may assume that the 14C(180, 2 0 0 ) "0 L A B E N E R G Y ( M e V )

l z C and 14C(180, 190)13C are essen- FIG. 1. - Excitation functions for 190, 200, and 21F from the

tially pure Zneutron and single-neutron transfer reaction 180

+

1x0.

Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphyscol:1971637

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C6-190 Y. EYAL, L. DOSTROVSKY A N D 2. F R A E N K E L

"0 L A B E N E R G Y ( M e V 1

FIG. 2.

-

Excitation functions for 16C. 17N, 1 9 0 and 2 0 0 from the reaction '$0 i '4C.

neutron transfer reaction cross section at bombarding energies in the neighborhood of the Coulomb barrier (22-24 MeV). This indicates that the two neutrons are transformed as a correlated pair, most likely with zero angular momentum. In figure 3 the excitation function of ' 8 0 ( 1 8 0 , 2 0 0 ) 1 6 0 below the Coulomb barrier is compared with the results of a calculation based on the DWBA method of Buttle and Goldfarb [I]

(solid line). These authors calculate the cross section for single neutron transfer between heavy ions at bombarding energies below the Coulomb barrier.

Since in our case the reaction products 160 and 200 are probably mainly produced in their ground states we have used the formula which applied to zero angular momentum transfer [I]. The absolute value of the calculated curve has been normalized to experi- mental results. It is seen in figure 3 that despite the fact that in our reactions two neutrons rather than one are transferred between the heavy ions, the shape of the calculated curve fits that of the experimental results reasonably well.

In figure 3 are also shown the experimental and calculated excitation functions for the 2-neutron transfer reaction 2 6 ~ g ( ' 8 0 , 160)28Mg. The expcri- mental reaction cross sections were obtained by bombarding natural magnesium targets 100- 1 200 pg/cm2 thick on 25 mglcm2 nickel backing with 180 ions. The 28Mg which was completely stopped in the target or backing was later separated radiochemically and the activity of the daughter nucleus 28A1 was measured by the P-y coincidence method. For the calculated curve we used the same formula as was used for the 180(180, 2 0 0 ) 1 G 0 reaction. However, in the present case the assumption of zero angular-momentum transfer is not justified

I I I , I I I I

2 0 25 20 25 30

Ie0 L A B ENERGY (MeV)

FIG. 3. - Experimental excitation functions of 180(180,

2 0 0 ) 1 6 0 and 26Mg(lKO, 160)28Mg below the Coulomb barrier.

Thc solid curves are rcsults of calculations based on theory of Buttle and Goldfarb [ I ]

.

since a sizeable fraction the 28Mg is created in its first excited state (1.468 MeV, 2'3. This is explained by the fact that unlike the Q-value for the 180('80,200)'60 reaction which is negative for all final states, the Q-value for the 26Mg(180, 160)28Mg is positive for the two first states of 28Mg (assuming

160 in its ground state). It is seen in figure 3 that indeed the shape of the calculated curve (which has been arbitrarily normalized to one experimental point) does not fit the experimental results.

In figures 4 and 5 we show the experimental angular distribution for the 2GMg('80, 160)28Mg reaction t o given final states at two bombarding energies.

These results were obtained by bombarding enriched (99.4 O/, '"g) magnesium targets of 80-100 pg/cm2 thickness on 15 pg/cm2 carbon backings with an

180 beam and detecting the two reactions products in two solid state detectors in coincidence. The most surprising result is the substantial fine structure in the angular distribution at the 180 laboratory energy of 33.5 MeV and the absence of the sizable structure at 35.7 MeV. We have tried to fit the diffraction model of Dar and Koslovsky [2] to the experimental angular distribution. The results are shown in the solid lines of figures 4 and 5. The calculations have been nor- malized to the experimental results by a least square fit. Whereas the 35.7t.MeV data could be fitted with

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TRANSFER REACTIONS BETWEEN 1 8 0 IONS A N D LIGHT NUCLEI C6-191

i I I 1 i

"Mg ("0, '60g,s) 28 Mgg 33.5 MeV T

and the cc diffuseness parameters >> d (d = 0.025 F) in order to fit the 33.5 MeV data (other parameters used : O , = 7 2 O , ro = 1.69 F).

160 CM ANGLE(de9) FIG. 5. - Center of mass angular distributions of - ' 6 0 from the

Frti. 4. - Center of mass angular distribution of 160 from the reactions 2 6 M ~ ( 1 a 0 , 1 6 0 ~ . ~ . ) 2 8 M g ~ . ~ . and 2 6 M d 1 8 0 . 2 6 0 g . ~ . ) reaction 26Mg(180, 160,.,,) 28Mg,,,, at 1 8 0 laboratory energy 28Mglstat labratory energy Of 35'7 MeV determined by the of 33.5 by the coincidence method. The curve coincidence method. The curves represent results of calculations

represents results of calculation by the diffraction model. by the diffraction model.

a cc reasonable )> set of parameters (8, = 660, Acknowledgement. - We are deeply grateful to ro = 1.60 F, Lo = 16 and d = 0.35 F (for definitions Professor P. Marmier for his generous hospitality and details see [ 2 ] ) we had to use unreasonably low and help which made the measurements at the E. T. H.

values for the cut-off angular momentum Lo (Lo = 9) Tandem Accelerator possible.

References

[ I ] BVTTLE (P. J. A.) a n d GOLDFARU (L. J. B.), NIICI. Phys., 1966, 78, 409.

[2] DAR (A.j and Koz~owsav (B.), P/zys. Rev. Letters, 1965, 15, 1036.

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