26.12.2012 Views

Radioactive beams by fragmentation and ISOL techniques - CERN

Radioactive beams by fragmentation and ISOL techniques - CERN

Radioactive beams by fragmentation and ISOL techniques - CERN

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

cmu Lxssasaexas, GENEVH<br />

|||l|||Ill||1|$||||l||I||llI|I|||1||}|||§I|l|IJIHII<br />

¤m@¤212a4<br />

RADIOACTIVE BEAMS BY FRAGMENTATION<br />

AND <strong>ISOL</strong> TECHNIQUES!<br />

W. Mittig<br />

GANIL, B.P. 5027, 14021 CAEN, France<br />

Invited contribution to the "lnteraational Workshop on <strong>Radioactive</strong><br />

Nuclear Beans produced <strong>by</strong> fragnent-separator techniquea", V<br />

arna, Bulgaria, October 12-15, 1993.<br />

GAN11. P 94 05 OCR Output<br />

g,.;w1L 3 “5*e·0`$<br />

Qw Qs *c®‘?>


OCR OutputRADIOACTIVE BEAMS BY FRAGMENTATION<br />

GANIL, B.P. 5027, 14021 CAEN, France<br />

Abstract: The general behaviour of <strong>fragmentation</strong> cross—sections lead to simple<br />

approximate analytical formulas. These formulas are used to compare the relative merits<br />

of the <strong>fragmentation</strong> <strong>and</strong> the Isol method to obtain radioactive <strong>beams</strong>. lt is seen that for<br />

<strong>beams</strong> with energies near the Coulomb barrier the Isol method gives much more intense<br />

<strong>beams</strong>, whereas for high energy, the <strong>fragmentation</strong> method is more effective. The break<br />

even is situated above or around 100 MeV/nucleon, the exact point depending on the<br />

relative Isol <strong>and</strong> spectrometer efficiency. OCR Output<br />

AND <strong>ISOL</strong> TECHNIQUES1)<br />

W. Mittig


intensity.<br />

During the last two decades, starting at LBL <strong>and</strong> continuing with high intensity<br />

high energy heavy ion <strong>beams</strong> at GANH., RIKEN, MSU <strong>and</strong> more recently at GSI/SIS.<br />

the <strong>fragmentation</strong> of the projectile was successfully used to produce secondary <strong>beams</strong>]<br />

Simultaneously, the <strong>ISOL</strong>—method (isotope separation on line) was used to produce low<br />

energy <strong>beams</strong> of 60 keV mainly for studies of decay <strong>and</strong> of ground state properties at<br />

<strong>ISOL</strong>DE/<strong>CERN</strong>2). The combination of these methods corresponds to the <strong>fragmentation</strong><br />

of the beam or the target <strong>and</strong> the reacceleration of the reaction products to energies high<br />

enough forstudies of nuclear reactions, this is of the order of 1-100 MeV/nucleon. The<br />

first <strong>beams</strong> using this method were obtained at Louvain—la-Neuve3). Various projects all<br />

over the world are very vigourously studied. A quite up-to—date compilation can be found<br />

in the proceedings of the Dourdan workshop4). I-Iere we dont want to discuss the relative<br />

merits of these projects but compare the <strong>fragmentation</strong> <strong>and</strong> the Isol methods for the<br />

production of high energy secondary <strong>beams</strong>.<br />

II. BEAM FRAGMENTATION<br />

In this section we deduce a simple formula which allows to estimate the intensity<br />

of a secondary beam produced <strong>by</strong> <strong>fragmentation</strong> <strong>and</strong> selected <strong>by</strong> a spectrometer. Three<br />

main points will be discussedza) the influence of the primary beam energy on the yield<br />

due to limited target thickness <strong>and</strong> spectrometer transmission, b) the choice of the primary<br />

beam, c) the effect of degrading of the the energy of the secondary beam energy on the<br />

a) Beam energy<br />

The use of the <strong>fragmentation</strong> of the projectile produces nuclei over a broad range<br />

of the nuclear chart. If the aim is the study of nuclei far from stability, a very selective<br />

device is needed, in order to have a high rejection of beam particles <strong>and</strong> of nuclei near<br />

stability, produced with several orders of magnitude higher yields. All recent studies have<br />

made use of magnetic spectrometers for such a selection. These spectrometers have a<br />

limited angular (A9, Arp) <strong>and</strong> momentum (Ap/p) acceptance.ln the following we will<br />

estimate the losses due to such a device.<br />

The variance ofthe distributions in the three dimensions (A0. Arp. Ap/phnay be<br />

estimated using the Goldhaberjl rule :<br />

é€f)<br />

Gimg = Ofcrmi -%,%-j OCR Output


where ofmg is the variance of the momentum distribution of the fragment, ofcimi<br />

is the fermi·momentum of about 100 MeV/c, <strong>and</strong> Af <strong>and</strong> AD the mass of the fragment <strong>and</strong><br />

the projectile respectively.<br />

(2)<br />

(4)<br />

The variance 0 of the distributions in 0, tp, Ap/p for a given fragment is then<br />

where Ei is the incident energy.<br />

An other important factor is the limitation of the target thickness due to energyloss<br />

differences between the incident <strong>and</strong> outgoing particle of atomic number Zi <strong>and</strong> Zi<br />

respectively. The energy loss in the target is approximately AE = CA2!/E where c is zi<br />

constant. The momentum spread introduced <strong>by</strong> the target of a thickness t is then<br />

We used the fact that the energy per nucleon before <strong>and</strong> after <strong>fragmentation</strong> is<br />

essentially the same. The maximum useful target thickness tom will be obtained if<br />

(Ap/p)img€i ~ omg/p; for thicker targets the loss in transmission due to broadening of the<br />

distributions will be stronger than the gain of yield due to a thicker target .<br />

The final yield y we will obtain for a given fragment is proportional the target<br />

thickness topi, <strong>and</strong> the angular <strong>and</strong> the momentum acceptance. If, as is the case very<br />

often, the acceptance of the spectrometer is smaller as than the width of the distribution.<br />

the yield ys at the exit of the spectrometer will be given <strong>by</strong><br />

Therefore the yield will increase with the incident energy in MeV/nucleon to the power<br />

7/2. The validity of ths formula can be checked <strong>by</strong> comparison with codes as LISEO) <strong>and</strong><br />

Intensity’l. This is shown on fig. l). Deviations observed for energies above several<br />

hundreds MeV/nucleon can be attributed to the fact that the distributions are no longer<br />

very broad as compared to the acceptance of the spectrometer. Where this happens is<br />

dependant on the reaction <strong>and</strong> the spectrometer acceptance considered. This can be seen<br />

<strong>by</strong> writing explicitly the A-dependance of the yield. Using equation (1). we otain. for<br />

example for G9 : OCR Output<br />

Ofrag ] ($9i:($(p:()'A :——o


(5)<br />

(4,)<br />

A A -A B<br />

69 = % = Gfumi IV ET`<br />

Z _ Sym DE V A;(Ap—l) Ap’Af<br />

Rewriting equation (4) gives<br />

YOc E?/2/UXP-1<br />

S (X)) P ‘ Af 3/2<br />

A quantitative formula can be easily obtained from the considerations above with<br />

of,ag=l()()MeV/c <strong>and</strong> Ei in units of MeV/nucleon<br />

YS=opmd.tOp[.(l) 3/2 Q?—.&.<br />

4,,) H G9 GQ? 6Ap/p<br />

Z 4.08 (5,,,.,., . t.,,,,(§§<br />

where SS, os, (Ap/p)S are the half acceptances of the spectrometer in units of<br />

radians <strong>and</strong> percent respectively This formula is valid as long as the acceptance is small<br />

as compared to the respective o—values of equation (5). Otherwise the gaussian<br />

distribution should be integrated using the error function. The final intensities can be<br />

obtained multiplying with the intensity of the incident beam.<br />

b) Choice of the beam<br />

A rough idea about the influence of the choice of the incident beam may be<br />

obtained <strong>by</strong> the following considerations.<br />

3/2 i*’l 30<br />

9, (D, . Ei<br />

The number of nuclei which will be produced can be approximated <strong>by</strong> the fact that<br />

the width of the isotope chains is approximately proportional to the atomic number Zbcam.<br />

Therefore for a constant total cross-section the cross-section will be devided <strong>by</strong> a number<br />

of channels which increases as Zi. As the energy loss is AE/E = cAZbcami/(EE)<br />

Zbeam for a given energy per nucleon we expect that the yield for a given channel in a<br />

<strong>fragmentation</strong> process will decrease as l/Zjbcam. This simple prediction is once again<br />

checked with respect to the codes LISE <strong>and</strong> Intensity on fig. 2.<br />

Thus, the beam should be choosen as light as possible to produce a given final<br />

product. However, one should not forget that more complicated processes than<br />

<strong>fragmentation</strong> contribute. Pick—up reactions for example may give significant yields. as OCR Output<br />

Q


1010<br />

8 10<br />

-A— —~ —Y‘ nd ES. 1 ) E? S<br />

10°<br />

104<br />

106<br />

105<br />

104<br />

1000<br />

100<br />

%<br />

100<br />

10 100 1000<br />

E (MeV/nuclcon)<br />

Fig 1: Prediction of secondary beam intensities <strong>by</strong> the programs LISE <strong>and</strong><br />

Intensity for a constant spectrometer acceptance compared tothe 7/2 E1aw,equ. (4).<br />

Z beam<br />

Fig 2: yield of 61-Ie as a function ofthe atomic number ofthe incident beum from<br />

LISE <strong>and</strong> Intensity codes(open circles) compared to the Z ‘—‘ lawttriunglesl. OCR Output<br />

10<br />

\\<br />

AV<br />

/ _ .<br />

/ c,<br />

/ Z<br />

\\<br />

100


37<br />

for example Si <strong>and</strong> 38 P observed with an 40Ar beam with sufficient yield to measure<br />

their massgl.<br />

product<br />

(5)<br />

c) Slowing down of energetic reaction products<br />

For several domains of physics, it is necessary to have low energy products. For<br />

example, interesting phenomena have been predicted in the fusion of neutron rich<br />

nuclei9). Energies of 1-5 MeV/nucleon are therefore necessary. These may be obtained <strong>by</strong><br />

slowing down the <strong>beams</strong> before the reaction. For a study of fusion of Be isotopes with<br />

an U target we measured the loss of intensity due to this slowing down]<br />

Slowing down in a thick degrader increases the absolute width of the momentum<br />

distribution. Writing a taylor serie to first order for Bpy as a fonction of Bp,<br />

Bp{=Bp{()+(dBpf/dBpi)ABri, we see that the initial width GA;)/p will be multiplied <strong>by</strong><br />

(dBpf/dBpi<br />

The transmission of the spectrometer is given <strong>by</strong> Ap/p, so even for a constant<br />

width a loss of transmission of Bpi/Bpf will result. Thus the loss factor fi will be the<br />

Fig. 3 shows that this relation holds experimentallyl<br />

An achromatic degrader could in principle give better results than a thick target. In<br />

practice, we found a yield 3 times lower than in the thick target case. The main reason is<br />

the limitation of spectrometers : with a thick target the straggling will add to the finite<br />

distribution of the nuclear reaction, <strong>and</strong> at least in the case studied here, the straggling is<br />

small as compared to the width of the nuclear reaction in the (9,q>, Ap/p) space. With an<br />

achromatic degrader, the Hrst part of the spectrometer already makes a severe cut in this<br />

space. A very thick degader will enlarge this distribution once again due to straggling.<br />

<strong>and</strong> it will be larger than the acceptance of the second part of the spectrometer, which is in<br />

most existing devices identical to the one of the first part. The conclusion may be<br />

different if the second part of the spectrometer has a very large acceptance. For the<br />

spectrometer LISEwe U) concluded, that it is more easy, more efficient <strong>and</strong> gives lower<br />

emittance <strong>beams</strong> if a thick target is used for simultaneous production <strong>and</strong> slowing down<br />

instead of the use of an achromatic degrader.<br />

For this case, we can use the analytical formulas of J.P. Dufour et allil. to<br />

estimate the loss . We get OCR Output<br />

f, 2 _<br />

dBp{ Bpi<br />

&Ea


(6)<br />

<strong>and</strong><br />

(8)<br />

(9)<br />

III. <strong>ISOL</strong> PRODUCTION<br />

incident beam can be used. This gives in a gain factor gl. Essentially all reaction products<br />

from beam or target <strong>fragmentation</strong> will be collected in the target. This corresponds to a<br />

gain gs with respect to a spectrometer, with gs = l/ts. Here, ts is the transmission of the<br />

spectrometer. For a given acceptance of a spectrometer, this gain factor gs will depend on<br />

energy as 1/Ei, 3/2as<br />

seen in equation (4).<br />

<strong>and</strong> reaccelerated. These different operations imply losses, which we will combine in the<br />

factor fisoi. So the ratio of the yield between the two methods i.e. lsol <strong>and</strong> beam<br />

fragemetation products, as a function of the incident energy <strong>and</strong> the final energy is<br />

(10)<br />

fl =<br />

(dBpi/Epi) _ 1<br />

(dBpr/Bpf) 1 - 4- `<br />

where R is the range of the secondary particle considered <strong>and</strong> d the thickness of the target<br />

between production <strong>and</strong> the end of the target. We have<br />

(7) Ef E(d) E, (1 ) R<br />

. f = E Y with Ei ~ 1.75 1 Y<br />

Combining with equation (4), the yield is<br />

3·5<br />

¤ _¤ y(Er,E1)< E{- E, {<br />

This equation will be used for the comparison with the <strong>ISOL</strong>-method.<br />

a) General considerations <strong>and</strong> comparison with beam <strong>fragmentation</strong><br />

Using the lSOL—method, a very thick target corresponding to the range of the<br />

However, in the lsol-method, the ions must be extracted from the target, ionized.<br />

where we approximated Y = 2. OCR Output<br />

R : Yisol = gigsfisol ,X {lsol fisol ·· (AKAI)-1 if/2<br />

YM; fi E?/2.fi 12?’2 Et A¤·Ar


The absolute value of R depends on the acceptance of the spectrometer<br />

12136<br />

considered. For a reaction C(C, He) we find, for fiSOi=1, R :1800 for the LISEO<br />

spectrometer <strong>and</strong> R :360 for SISSI13), for Ei = Ef <strong>and</strong> Ei : 50 MeV/nucleon. ln the<br />

following we will use R :500.<br />

MeV/nucleon.<br />

We can now plot the behaviour of R as a function of incident energy, using<br />

equation (10) on fig 4). In order to limit the number of parameters, we fixed Ef : 5<br />

This figure 4) should be considered as qualitative, because as stated above, the<br />

exact value or R depends on the spectrometer acceptance <strong>and</strong> on the reaction considered.<br />

However, it allows us a general conclusion: if experiments with the secondary beam are<br />

to be done at the energy of the primary beam (in units/nucleon), there is a break even<br />

point of both methods at around 100 MeV/nucleon if the final yield is considered for a<br />

given incident beam intensity The exact value of this energy depends on the <strong>ISOL</strong><br />

efficiency <strong>and</strong> the spectrometer characteristics considered.<br />

lf low energy secondary <strong>beams</strong> are needed, the gain factor of the lsol method with<br />

respect to slowed down products increase with the energy of the primary beam. So, for<br />

low energies of the secondary <strong>beams</strong> the lsol method gives higher intensities <strong>and</strong> better<br />

beam quality as long as the lsol efficiency is in a reasonable range (fisoi > 10*). For an<br />

energy of the primary beam of about 100MeV/nucleon <strong>and</strong> of a final energy of<br />

5MeV/nucleori the ratio R is about 1000 for fiSOi:0.0l as can be seen on figure 4)<br />

b)Beams for <strong>ISOL</strong>-<strong>techniques</strong><br />

Up to now, we considered the same beam for the production of secondary <strong>beams</strong><br />

<strong>by</strong> <strong>fragmentation</strong> <strong>and</strong> <strong>ISOL</strong> <strong>techniques</strong>. In the lsol <strong>techniques</strong> the beam <strong>and</strong> the target<br />

may be choosen more independantly than in the direct <strong>fragmentation</strong> technique, if target<br />

residues are used. This means essentially that light ion <strong>beams</strong> of high intensity may be<br />

used, such as high energy proton <strong>beams</strong>.<br />

Here a delicate balance of production cross-section, range, <strong>and</strong> extraction<br />

efficiency from the target will determine if light ion <strong>beams</strong> or heavy ion <strong>beams</strong> are more<br />

efficient. As a general thumbrule, it turns out that heavy ion <strong>beams</strong> are. at same beam<br />

power in units of Watt. are better for the production of ions below A ~100. whereas light<br />

ion <strong>beams</strong> are more efficient for the production of secondary <strong>beams</strong> with A>l()0. Actual<br />

limits for heavy ion <strong>beams</strong> in the 1 GeV region are 1-10 kW. Proton <strong>beams</strong> with about 1<br />

GeV <strong>and</strong> more than 100 kW exist, <strong>and</strong> may be the most promising long range possibility<br />

for the production of secondary <strong>beams</strong>. R+D programs for the use of these very intense<br />

<strong>beams</strong> exist at Triumphm), PSIIS) <strong>and</strong> RAU6) <strong>and</strong> may show that the use of these very<br />

intense <strong>beams</strong> for the present purpose is practical. A more detailed discussion may be<br />

found in reference 17.18). OCR Output


5,, 1000<br />

0.8<br />

’·· 0.6<br />

0.1<br />

0.4<br />

0.2 l—<br />

105<br />

10<br />

I0<br />

0 0.2 0.4 0.6 0.8 1 1 .2<br />

before slowing down Ii (see equation 5)<br />

&....=1<br />

Q\`~<br />

» - - ·i ’ "'<br />

fl$0I=0·01<br />

Fig 4: Ratio of Isol <strong>and</strong> beam—<strong>fragmentation</strong> secondary beam intensities as a function of<br />

the primary beam intensity. In the last case it is supposed that the secondary beam is<br />

selected <strong>by</strong> a spectrometer It is shown for two Isol efficiencies, <strong>and</strong> two cases of the<br />

energy ofthe secondary beam, one is constant 5 MeV/nucleon, the other is equal to the<br />

primary beam energy. Note that this graph is only qualitative, it depends on the reaction<br />

<strong>and</strong> the spectrometer acceptance (see text). OCR Output<br />

(dBm/dBpf>


emittance.<br />

If a broad range of nuclei far from stability are to be produced, a total energy of<br />

about l GeV in the composite system is needed. Lower total energies will give more<br />

localised populations of the nuclear chart, thus giving higher cross—sections for nuclei<br />

near the stability, however the cross-section far from stability will drop much faster. This<br />

is, for example, the case for the Arenas device at Louvain la Neuvel9), where a 30 MeV<br />

proton beam was used, <strong>and</strong> for the Oak Ridgem) project.<br />

c) Special problems of the Isol <strong>techniques</strong><br />

The <strong>ISOL</strong> technique needs the extraction of the secondary ions out of the target<br />

material, the ionisation <strong>and</strong> reacceleration of these ions. Due to different physico-chemical<br />

behaviour each element has different problems. The 20 years of experience of<br />

<strong>ISOL</strong>DE/<strong>CERN</strong> show simultaneously that these problems may be solved for most of the<br />

elements, <strong>and</strong> however for each element a lot of R+D is required to get optimum results.<br />

Besides the chemical behaviour, the diffusion—effusion time from the target to the<br />

ion source is a difficultfproblems. The diffusion out of the target is determined mainly <strong>by</strong><br />

the mechanical structure of the target <strong>and</strong> the temperature, the effusion from the target to<br />

the ion source <strong>by</strong> the sticking time of the atoms to the walls. Typical total delay times are<br />

of the order of secondsm). This may be a serious h<strong>and</strong>icap for very short lived ions.<br />

The atoms must be ionised, <strong>and</strong> here other losses will occur. Three possibilities<br />

are studied <strong>and</strong>/or used actually: production of negative ions for use in t<strong>and</strong>ems.<br />

production of singly charged positive ions, <strong>and</strong> multiple charged ions. With modern<br />

ECR—sources the last possibility is promising, however a lot of R+D is still necessary to<br />

make this possibility operational for a broad range of elements <strong>and</strong> of live—times together<br />

with a high power (~lO kW) beam incident on the target near the plasma. Acceleration<br />

will imply further losses, depending on the acceleration mode choosen, efficiency of<br />

stripping if necessary in the acceleration mode chosen, <strong>and</strong> on the initial ion source<br />

Following the preceeding considerations, it is clear that no general num ber exists<br />

for the total <strong>ISOL</strong> efficiency. Best numbers which may be expected for a multi-charged<br />

ion source followed <strong>by</strong> a cyclotron as at Louvain la Neuve <strong>and</strong> as in the Ganil—Spirale<br />

project may be taken to be 2 x 10%, using 20 % for the total target + ionisation<br />

efficiency, 20 % for the most probable charge state, <strong>and</strong> 50 % for the acceleration<br />

efficiency. Actual best results are about l order of magnitude below this number.<br />

These problems are avoided in direct use of <strong>fragmentation</strong> products. where short<br />

life-times of down to l tts are available, <strong>and</strong> no chemical selectivity exists. OCR Output


Referen<br />

The <strong>ISOL</strong>—method will give <strong>beams</strong> of good emittance, the same as the one of<br />

primary <strong>beams</strong>. It will in most cases purify the <strong>beams</strong> <strong>by</strong> the specific selectivity of the ion<br />

source <strong>and</strong> the accelerator. In the case of secondary <strong>beams</strong> <strong>by</strong> <strong>fragmentation</strong>, the<br />

emittance is determined <strong>by</strong> the target thickness <strong>and</strong> the nuclear reaction, <strong>and</strong> will<br />

correspond in most cases to the acceptance of the beam-lines. This may be a h<strong>and</strong>icap for<br />

the study of nuclear reactions induced <strong>by</strong> these ions. It may be overcome <strong>by</strong> tagging the<br />

incoming particles, determining their characteristics event <strong>by</strong> event. This will limit the<br />

intensity of the secondary beam below 106/s. Severe losses can occur <strong>by</strong> the purification<br />

of the beam, due to increase of emittance <strong>and</strong> charge exchange in degraders <strong>and</strong>/or other<br />

filters. Purification will often be necessary in order to separate the rare ions of interest<br />

from much more frequent other ions, transmitted even after a magnetic rigidity selection.<br />

These losses were not included in the numbers for figure 4) <strong>and</strong> in equation (l()).<br />

V.C0nclusi0n<br />

The <strong>ISOL</strong>—technique for the production of energetic secondary <strong>beams</strong> opens new<br />

perspectives for the study of nuclear structure far from stability because it offers or will<br />

offer several oders of mgnitude of increase in intensity of good quality, pure secondary<br />

<strong>beams</strong>. With the actual <strong>techniques</strong>, the domain where this method is most advantageous<br />

with respect to the direct use of <strong>fragmentation</strong> products of the beam is at energies around<br />

the Coulomb-barrier. A breakeven of secondary beam intensities obtained from these two<br />

methods occurs at an energy of the secondary beam above or around l()OMeV/nucleon if<br />

the primary beam considered is the same.<br />

The author thanks A.C.C.Villari for a careful reading of the manuscript.<br />

1) see for example the proceedings of the first international Conference on<br />

"<strong>Radioactive</strong> Nuclear Beams", Berkeley, oct 1991. ed W.D.l\/Iyers. J.l\/l.Nitschke.<br />

E.B.Norman,World Scientific<br />

2) B.W.Allardyce, H.L.Ravn, <strong>and</strong> the Isolde Collaboration, NIM B26(l987)l I2 OCR Output


367, 375, 391<br />

3) see the proceedings of the Second International Conference on <strong>Radioactive</strong><br />

Nuclear Beams, Louvain la Neuve, august 1991, pages 121, 173, 265, 277, 279, 281,<br />

B70(1987)215<br />

4) Proceedings of the international Workshop on Physics <strong>and</strong> Techniques of<br />

Secondary Nuclear Beams, Dourdan, pages 311-452, France,march 1992 ed<br />

J.F.Bru<strong>and</strong>et, B.Fern<strong>and</strong>ez, M,Bex, editions frontieres,France<br />

5) A.S.Goldhaber, Phys.Lett. 53B(1974)306<br />

6) D.Bazin, private communication<br />

7) J.A.Winger, B.M. Sherrill, <strong>and</strong> D.J.Morrissey,NIMB70(1992)380<br />

8) A.Gillibert, W.Mittig, L.Bianchi, A.Cunsolo, B.Fern<strong>and</strong>ez, A.Foti,<br />

J.Gastebois, C.Gregoire, Y.Schutz,<strong>and</strong> C.Stephan, Phys.Lett.B192(1987)39<br />

9) M.S.Hussein et al,Phys.Rev.C46(1992)377<br />

10) Yang Yong Feng, W.Mittig, J.L.Sida,P.Roussel-Chomaz, M.Lewitowicz,<br />

N.Alamanos, F.Auger, C.Borcea, C.Cabot, A.Cunsolo, A.Foti, A.Gillibert <strong>and</strong><br />

C.Volant, NIM B82(1993)175<br />

11) R.Anne, D.Bazin, A.C.Mueller, J.C.Jacmart, <strong>and</strong> M.Langevin. _NlM<br />

12) J.P.Dufour, R.del Moral, I-I.Emmermann, F.}-Iubert, D.Jean, C.Poinot.<br />

M.S.Pravikoff <strong>and</strong> A.F1eury NIMA248(1986)267<br />

13) C.Grunberg, D.Larson, W.Mittig, F.Ripouteau, preprint Ganil R 89-09<br />

14) I.D.D'Auria, M.Domsky, L.Buchmann, H.Sprenger, J.Vincent,proceedings<br />

of the first intemational Conference on "<strong>Radioactive</strong> Nuclear Beams", page 34, Berkeley.<br />

oct 1991, ed W.D.Myers, J.M.Nitschke, E.B.Norman,World Scientific<br />

15) I-I.W.Gaeggeler, I-I.W.Drissi, S.Kern, proceedings of the Physics <strong>and</strong><br />

Techniques of Secondary Nuclear Beams, Dourdan, page 429, France,march 1992 ed<br />

J.F.Bru<strong>and</strong>et, B.Fern<strong>and</strong>ez, M,Bex, editiond frontieres,France<br />

16) see the NUPECC report may 1993, Europeen <strong>Radioactive</strong> Beam Facilities<br />

17) idem<br />

18) the IsoSpin Laboratory, LALP-91-51 <strong>and</strong> J.D.Garrett,proceedings of the<br />

Physics <strong>and</strong> Techniques of Secondary Nuclear Beams, Dourdan, page 311.<br />

France,march 1992 ed J.F.Bm<strong>and</strong>et, B.Fem<strong>and</strong>ez, M,Bex, editiond frontieres,France<br />

19) see 16) <strong>and</strong> P.Decrock et al,proceedings of the Physics <strong>and</strong> Techniques of<br />

Secondary Nuclear Beams, Dourdan, page 423, France,march 1992 ed l.F.Bru<strong>and</strong>et.<br />

B.Fern<strong>and</strong>ez, M,Bex, editiond frontieres,France<br />

20) Physics with radioactive <strong>beams</strong> at the I-lolifield Heavy Ion Research<br />

Facility,Oakridge, 1990, preprint<br />

21) K.Kirchner, NIM B70(1992)165, NIM A292(l990)203

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!