Possibility of bringing TRI  P to HIE-ISOLDE Dual magnetic Spectrometer Olof TENGBLAD ISCC Oct. 22nd 2013 There will be a presentation during the ISOLDE.

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Presentation transcript:

Possibility of bringing TRI  P to HIE-ISOLDE Dual magnetic Spectrometer Olof TENGBLAD ISCC Oct. 22nd 2013 There will be a presentation during the ISOLDE workshop November by Lorens Willman from the TRI  P collaboration at KVI. But as not everyone will be present I will give some background and some explanation to what the TRI  P is and how it could fit at HIE-ISOLDE.

Zero-degree Hie-Isolde 2 Workshop in LUND March 2011 where it was expressed a strong interest for having a Zero- degree spectrometer coupled to HIE-ISOLDE. The initiative was postpone due to the rapid advance of the TSR project and two such projects on the same time was too much

INCIDENT BEAM (d,t) forward of 45° (d,d) just forward of 90° (d,p) from 180° to forward of 80° transfer products on neutron-rich side can sequentially n-decay USING RADIOACTIVE BEAMS in INVERSE KINEMATICS isobaric beams can be identified and/or physically separated (possibly further stripped, e.g. 15 N 3+ / 21 O 4+ ) Knock-on carbons from CD 2 targets fusion-evaporation products from reactions on C in CD 2 targets WHY a Zero-degree spectrometer Wilton Catford University of Surrey, UK

26 Ne(d,p) 27 Ne 26 Ne(d,p) 27 Ne  26 Ne+n ZERO DEGREE = SPECTROMETER ZERO DEGREE = SCINTILLATOR RESULTS from TIARA/MUST2 Nov2007RESULTS from SHARC Aug2009 Energy v Theta with trifoil 26 Na g.s. 26 Na ex. states (d,d) (p,p) 25 Na(d,p) 26 Na 5 A.MeV Wilton Catford University of Surrey, UK

Original KVI 5 27 August 1999 This is not some old equipment laying around. Original proposal for funding in August 1999, to build a “Microlaboratorie for fundamental Physics at KVI using Trapped radioactive Isotopes” 2001 Start building – 2005 ready for Beam 4.6 M€ project, where the Recoil separatar was 1.7 M€.

6 TRI  The radioactive nuclei are produced using beams from the superconducting cyclotron AGOR. The high energy radioactive beam is transformed to a low-energy. High quality bunched beam by the combined fragment and recoil-separator.

TRI  P test beam report

TRI  P separator 8 B1-B4 4 dipole- & Q1-Q9 8 quadrupole- magnets Q3 was omitted in final design Slits Sec. 1 Dispersion: Separate isotopes of different rigidity Sec. 2 reversed:  Achromatic image Dipole magnets H-type DANFYSIK

Fragmentation mode m m 20 mm 10 mm Target spot size +/-2 mm horizontal +/- 1 mm vertical

10 The time of flight vs. energy loss in a 100 mm silicon detector shows various nuclides at the intermediate plane (T2). At the final focal plane (T3) there is only 21 Na and a small contamination of stable 20 Ne which could be reduced to below 0.5 % 21 Ne(p,n) 21 Na 21 Ne 43 MeV/u on 20 mg/cm 2 polyethylen target The emerging primary beam now 21 Ne 10+ is stopped in slits SH2

11 15 N( d,p ) 16 N 16 N separated & implanted in a DSSSD. For beta decay study P20 ENSAR supported experiment in N from AGOR on Deuterated gas T1  the produced 16 N was separated and transported and slowed down to be implanted in a micro strip detector to measure. 16 N   16 O +  measure the summed deposit energy R. Raabe & H. Fynbo TRI  P is new equipment still in use & with an existing collaboration.

12 TRI  P with MiniBall MiniBall

What would an ideal zero-degree device achieve? identification of reaction products physical separation of reaction products  beam physical separation of reaction products  fusion-evaporation physical separation of isobaric beams or other beam contaminants large enough angular acceptance to pick up sequential decay products excellent angular resolution to allow kinematic reconstruction – missing-p