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Submitted on 1 Jan 1975
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Saintignon
To cite this version:
HOW DOES THE
ELASTIC SCATTERING OF
12C
+20Ne
COMPARE WITH THAT OF
16O
+16O ?
H.
DOUBRE,
E. PLAGNOL(*),
J. C. ROYNETTEInstitut de
Physique
Nucléaire,
BP1,
91406Orsay,
Franceand
J. M.
LOISEAUX,
P.MARTIN,
P. de SAINTIGNON Institut des SciencesNucléaires,
BP257,
38044Grenoble,
FranceRésumé. - Les fonctions d’excitation de
cinq voies de sortie du système 12C + 20Ne entre
22 et 28 MeV (C.M.) présentent une structure importante à 90° et 130° (C.M.). Cette structure, analogue à celle qu’on observe
pour
16O + 16O est analysée en termes d’accord des momentsangulaires.
On présente une distribution angulaire à 24,7 MeV (C.M.). Il est montré quel’absorption
due aux voies directes est intermédiaire entre celle de 16O + 16O et 18O + 18O.
Abstract. - Excitation functions for 5 exit channels of the 12C + 20Ne
system are given in the range 22-28 MeV centre of mass incident energy. An important structure is observed in the elastic scattering excitation functions taken at 90° and 130° (C.M.). This structure, which reminds one of the 16O + 16O case, is studied in terms of angular momentum matching. An angular distribution taken at 24.7 MeV (C.M.) is also presented. The direct channel absorption is shown to be inter-mediate between the 16O + 16O and 18O + 18O cases.
Since the observation
[1]
of a strong gross structurein
the 160
+16 0
elasticscattering
functions,
many other systems of identical or non identicallight
nuclei have been studied
[2].
It was soonrecognized
that the observed structure is not a
specific
featureof identical
particles (i.e.
not due to the lack ofodd-partial
waves in thescattering amplitude)
as the180 + 180
system shows astrongly damped
struc-ture and a small average cross-section.Upon
consi-derations onangular
momentummatching
between the entrance channel and the reactionchannels,
it wassuggested [3]
that thepronounced
structure and thelarge
cross-sections observed in the160 + 160
elastic
scattering
were related to theinability
for this system to carry awaythrough
the direct reaction channels thelarge
angular
momentumbrought
inby
thegrazing
waves of the entrance channel. Interms of
optical-model
parameters, thisimplies
thatthe
magnitude
of the average cross-section isroughly
determinedby
thestrength
of theimaginary
potential,
whereas thepeak-to-valley
ratiocritically depends
on its transparency for thegrazing
partial
waves.Such an
interpretation
seems to bestrongly supported
by
theimpressive improvements
of the fits to the(*) Now at S.P.N.B.E., C.E.N. Saclay, BP 2, 91190
Gif-sur-Yvette, France.
experimental
data,
obtained when an1-dependent
imaginary
potential
is used[4].
Potentials of this type are able toexplain
the appearance ofshape
resonances. The
existence,
in the160( 160,
12C)
2 ONe
reaction
[5, 6]
of a similar structure has beeninterpret-ed as evidence for such a mechanism. This
coupling
may,however,
also beexplained
by
considerationsbased on the
I-space
localisation of the4-particle
transfer
[6], [11].
From thisviewpoint,
thecomparison
of the12C
+2°Ne
system with the160
+ 160 system is of interest. In terms ofangular
momentummatching,
it has been shownby
Vandenbosch,
Webb and Zisman[7]
that some differences shouldexist between them and result in a more
damped
structure and smaller cross-sections in
the 12C
+2°Ne
system. This seems to besupported by
theirdata,
which was however limited for
experimental
reasonsto smaller
(80°)
centre of mass(C.M.)
angles.
In thisletter,
we present excitation functions ofthe
12C
+2°Ne
system for the elastic channel and the 4 reaction channels which are best matched withthe entrance channel. These measurements,
performed
at
70°,
90° and 1300(C.M.)
show for the backwardangles
someinteresting
differences with the conclu-sions of reference[7].
An elasticscattering
angular
distribution at 24.7 MeV(C.M.)
incident energy is alsogiven.
I.S.N. Grenoble
Cyclotron.
The beam energy, asmeasured
by
magnetic
analysis,
is considered to beknown within an absolute accuracy of 500 keV
(lab.),
and the energydispersion
of the beam to beapproxi-mately
400 keV(lab.),
that is 150 keV(C.M.).
Several values of beam energy for the excitation functionswere obtained
by slowing
down the incident ionsthrough
carbon foils. It was checked that the beamquality
suffered nosignificant
deterioration.The
experimental
set-upcomprised
two differentsystems of detection. For centre of mass
angles
close to90°,
particles
were identifiedby
theassociated-particle
method in two 200mm2
solid-state surface-barrier detectors. One waskept
fixed at 45°(lab.)
while the
position
of the other wasadjusted
to obtain the maximumcounting
rate. For the excitation function measurements, the solidangle
was aslarge
as 2.4 msr. Thepresented
excitation functions areaveraged
over a ± 3°(C.M.)
horizontalangle.
Forthe elastic
scattering angular
distribution,
this valuewas
brought
down to ± 1°(C.M.).
With this system, the energy resolution was limitedmainly by
thetarget thickness
(100
Jlgjcm2)
andby
the beam energydispersion.
Special
care was taken to make sure ofthe maximum
efficiency
of the system, but nocorrec-tion has been
applied
(e.g.
for inflight
gammadecay
of an excited nucleus or
multiple scattering).
The otherdetecting
system was a standard AE - Etelescope
(10 ~m)
for detection and identification of reactionproducts
emitted in a 0.2 msr. solidangle
at alaboratory angle
~ 25°(lab.),
(i.e.
70°(C.M.)
if 2°Ne are detected or > 130°(C.M.)
ifrecoil 12C are
detected).
Energy
resolution inFIG. 1. - Excitation functions of the 12C
+ 2°Ne elastic scattering thick full curve guides the eye between experimental points thin full line = optical model predictions with the potential of refe-rence [8] dashed line = optical model predictions with the potential
of reference [7] (see text).
cross-sections are
given
within an accuracy of 25%.
The elasticscattering
excitation functions appearin
figure
1. At 700(C.M.),
it isstrongly
decreasing,
without any strong structure and in excellent
agree-ment with the results of
Vandenbosch,
Webb andZisman
[7].
Excitation functions at 700 for the12C
+ 2 °Ne and the 160
+ 160 systems werecompar-ed in reference
[7].
It was concluded that the differentbehaviour of the excitation functions was due to a
larger absorption
forhigh
1-values in the12C
+2°Ne
case. In contrast with what is observed at
700,
both the 900(C.M.)
and the 1300(C.M.)
elasticscattering
excitation functionsclearly
show a structure. It is well-knownthat,
at 900(C.M.)
the absence ofodd-partial
waves in thescattering amplitude
cangive
morepronounced
structure to thecross-section,
but this argument nolonger
holds at 1300 where a similarstructure is observed. The 900 excitation function is
quite
comparable
to the 160 + 160 one at the sameangle.
The main differences are in thepeak-to-valley
ratio,
which isslightly
smaller(though
the limited energy andangular
resolution of thisexperi-ment can account for some reduction of this
value),
and in the absolute values of thecross-sections,
one order ofmagnitude
smaller for12C
+2°Ne,
evenif the
identity
ofparticles
in the 160 +160
systemis taken into account.
FIG. 2. - Angular distribution of the 12C + 2°Ne elastic
scattering ,
at 24.7 MeV (C.M.). Full line = optical model predictions with the
potential of reference [7]. Dashed line = optical model predictions
As shown in the same
figure,
theexperimental
data lie between thepredictions
of theoptical-model
potential proposed
in reference[7]
for12C
+2°Ne
and of Gobbi’s
potential
[8]
applied
to the samesystem. The latter appears to be too transparent
whereas the former allows for too much
absorption.
It is
interesting
to note that thedisagreement
between the data andpredictions
of theoptical-model
poten-tial of reference[7]
increases withangle.
Such aconclusion is also
supported
by
figure
2 where theangular
distribution at 24.7 MeV(C.M.)
incidentFIG. 3. - Excitation functions for the reaction channels 1606-7MeV corresponds to the 4 excited states of 160 at 6.05 MeV (0+), 6.13 MeV (3-), 6.92 MeV (2+) and 7.12 MeV (1-), at ~c.M. ~ 62~.
In
figure
3 arepresented
the excitation functionsfor several reaction
channels,
namely
the inelasticscattering
to the2+,
(1.63 MeV)
and the4+,
(4.25 MeV)
excited states of2 °Ne,
and the4-particle
transfers to theground
state and to the 6-7 MeV excitationenergy doublets in 160. These channels were chosen
because of their
ability
to carry away theangular
momentum
brought
inby
the entrance channel.A strong structure
only
appears for the4-particle
transfer
leading
to theground
stateof 160,
for whichthe results agree with those of the inverse reaction
studied in reference
[5].
The lack of structure in theinelastic
scattering
excitation function should notbe too
surprising.
This isstrongly
reminiscent of160+
160 inelasticscattering
where,
with acompa-rable
angular
momentummatching,
there is nostructure in the inelastic excitation function.
4-particle
energy is
compared
to the sameoptical-model
pre-dictions.
Up
to 700 the strong decrease of the cross-section withangle
may beinterpreted
as due to a strongabsorption,
asproposed
in reference[7].
At morebackward
angles,
theangular
distribution is veryrapidly
oscillating,
with aperiod
close to 1 ()ü(C.M.).
Eventhough
it does not extend to the utmost back-wardangles,
it shows no evidence for an elastictransfer
contribution,
which would involve a veryimprobable 8-particle
transfer.transfer to the 6-7 MeV doublets of
160
presents a moreintriguing
behaviour. From1-matching
consi-derations,
the 3 - component of these doublets is in a favorableposition
andaccording
to theanalysis
performed
by
Rossner et al.[6],
this shouldimply
a
large
crosssection,
whereas the0+,
1- and 2+levels should exhibit smaller cross sections. The data collected so far
indicate,
quite contrarily,
that the contributions of bothdoublets
are of the same orderof
magnitude.
To elucidate thisunexpected
andinteresting
behaviour,
a morecomplete
experimental
and theoretical
analysis
is necessary.Finally,
it could be worthwile to mention a small butpersistent irregularity
present on every excitationfunction at about 25 MeV. However, such an
irregu-larity
does not appear in the2°Ne(12C, a)2gSi
data160 + 16 0 and 180 + 180 systems with
regard
to both the structure and themagnitude
of the cross-sections. This can be related to the factthat,
in thiscase,
only
few direct reaction channels are able tocarry away the entrance
angular
momentum, whereasin the 180 +
180
case, a verylarge
number of chan-nels exist. In the 160 + 160 case, there are none,at least up to 30 MeV
(C.M.)
incident energy. Asthe energy
rises,
the still limited number of thesereactions channels
increases,
resulting
in a reductionof the observed elastic cross-section with however a
persistent
structure[10].
In the1.2C
+2 °Ne
case,the
integrated
cross-sections of these channels(2+
and 4+ inelastic
scattering)
werecrudely
evaluatedand amount to about 100-150 mb. It can be noticed
the intermediate behaviour of the
12C
+ 2°Ne elasticscattering.
Finally,
thestudy
of the12c
+2°Ne
systemconfirms
nicely
thatangular
momentumconsidera-tions
[3]
canprovide
a reliable tool forpredicting
thequalitative
differences forabsorption
inheavy
ion reactions.Acknowledgments.
- Three ofus
(H.
D.,
E. P. and J. C.R.)
thank Professor J. Valentin for his kindhospitality
and thecyclotron
crew for efficientoperation.
We thank Professor P. P.
Singh
and Dr. A.Weidin-ger for many
enlightening,
discussions.References
[1] SIEMSSEN, R. H., MAHER, J. V., WEIDINGER, A. and BROMLEY,
D. A., Phys. Rev. Lett. 19 (1967) 369.
[2] See, for instance, SIEMSSEN, R. H. in Heavy ion scattering,
Argonne National Laboratory Report ANL 7837 (1971)
unpublished.
[3] VANDENBOSCH, R., in Heavy ion scattering, Argonne National
Laboratory Report ANL 7837 (1971) unpublished.
[4] CHATVIN, R. A., ECK, J. S., ROBSON, D. and RICHTER, A.,
Phys. Rev. C 1 (1970) 795.
[5] SINGH, P..P. et al., Phys. Rev. Lett. 28 (1972) 1714.
[6] ROSSNER, H. H., HINDERER, G., WEIDINGER, A. and EBERHARD,
K. A., Nucl. Phys. A 218 (1974) 605.
[7] VANDENBOSCH, R., WEBB, M. P. and ZISMAN, M. S., Phys.
Rev. Lett. 33 (1974) 842.
[8] GOBBI, A. et al., Phys. Rev. C 7 (1973) 30.
[9] COSNAN, E. R. et al., Bull. Am. Phys. Soc. 18 (1973) 565.
[10] HALBERT, M. L. et al., Phys. Lett. B 51 (1974) 345.