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<strong>GSI</strong>-UPGRADE-ACC-09 <strong>GSI</strong> SCIENTIFIC REPORT 2009<br />

154<br />

<strong>GSI</strong>Template2007<br />

Status of the SIS 18 Vacuum Upgrade*<br />

M.C.Bellachioma, M.Bender, J. Cavaco, H. Kollmus, A. Kraemer, J. Kurdal, and H. Reich-Sprenger<br />

<strong>GSI</strong>, Darmstadt, Germany.<br />

In the context of the technical developments for the<br />

construction of the Facility for Antiproton and Ion Research<br />

at <strong>GSI</strong>, an intensive programme for the vacuum<br />

upgrade of the existing heavy ion synchrotron (SIS 18)<br />

was started in 2005, with the aim to improve the beam<br />

lifetime and the beam intensity. To reach these purposes<br />

the installation of NEG coated dipole and quadrupole<br />

chambers was foreseen, and additionally to overcome the<br />

dynamic vacuum instability a collimation system<br />

equipped with thin film coated absorbers was designed<br />

and commissioned.<br />

The production of the thin film getter was carried out in<br />

two cylindrical magnetron sputtering facilities described<br />

in details in Ref. [1]. The surface chemical composition<br />

and the good activation behaviour of the produced thin<br />

films (≈ 1μm thick) were proved at CERN and at the<br />

Magdeburg University by X-ray Photoelectron Spectroscopy<br />

(XPS). Considering that the vacuum chambers<br />

mounted in accelerators undergo several ventingactivation<br />

cycles, a deep investigation on the NEG ageing<br />

was performed last year at <strong>GSI</strong> by Elastic Recoil Detection<br />

Analysis (ERDA) [2]. In each activation cycle an<br />

identical quantity of oxygen is dissolved in the film bulk.<br />

However heating at temperatures lower than 250°C (as<br />

performed for the <strong>GSI</strong> coated chambers) does not allow a<br />

uniform oxygen concentration to be reached in the film<br />

and, as a consequence, oxygen atoms are settled in the<br />

film to form a concentration profile with the maximum<br />

close to the surface (see fig.1) which finally leads to accelerated<br />

performance degradation. The film degradation<br />

can be also explained in terms of C accumulation on the<br />

surface; in effect this element needs a higher heating temperature<br />

to be dissolved in the film bulk [3]. An abrupt<br />

reduction of the pumping speed was observed for thin<br />

coatings (0.25μm) after about 12 cycles when heating at<br />

200°C [4].<br />

Figure 1: The number of activation cycle is plotted from<br />

light to dark colour, carbon in red and oxygen in blue.<br />

* Work supported by EU design study, DIRAC-PHASE-<br />

1 RP6 SIS18-2 contract No. 515876.<br />

# cee@aps.anl.gov<br />

In parallel to the production and characterisation of the<br />

thin film getters an ion catcher system was designed and<br />

commissioned to guarantee that the loss of the charge<br />

exchanged particles behind the dipole chambers of the<br />

SIS 18 occurs on a low desorbing material and in a high<br />

pumping environment (assured by a NEG thin film).<br />

Lowest desorption was observed for gold coated copper<br />

targets, where a thin nickel film between copper and gold<br />

avoid diffusion of the materials into each other during the<br />

standard UHV bakeout. For this purpose a Ni film thickness<br />

around 200nm is sufficient [2, 5].<br />

Initially two geometries were realized: a wedge and a<br />

<strong>block</strong> shaped absorber. The first one, which separates the<br />

region where the losses occur from the circulating beam,<br />

has the disadvantage that the particles hit the absorber<br />

under grazing incident causing high desorption. The second<br />

one, which can be placed in the correct position by a<br />

linear motion feedthrough guarantees instead perpendicular<br />

incident with the disadvantage of an open geometry.<br />

Experiments have shown [5] that the <strong>block</strong> shaped absorber<br />

has a lower desorption yield on the level of 25<br />

molecules per incident ion. Therefore it represents the<br />

favourite solution for the ion catcher system.<br />

At the end of 2008 two ion catcher prototypes, 14<br />

coated dipole chambers and one quadrupole chamber<br />

were implemented in the SIS18. First experiments to<br />

evaluate the vacuum upgrade achievement showed a clear<br />

improvement in achievable U 28+ beam lifetime caused by<br />

the upgraded UHV system [6].<br />

During the 2 upgrade shutdowns in 2009 all the remaining<br />

coated dipole and quadrupole (except for the one in<br />

S11) chambers and ten ion catcher were mounted in the<br />

accelerator. In summary, during the upgrade shutdowns<br />

from 2006 to 2009 24 dipole magnet chambers, 11 long<br />

quadrupole chambers, 5 short quadrupole chambers, 10<br />

collimator chambers and 5 straight vacuum chambers<br />

were replaced by NEG-coated UHV chambers, which<br />

corresponds to app. 65% of the SIS 18 circumference.<br />

Commissioning of the UHV system upgraded will be performed<br />

in the beginning of 2010. Detailed measurements<br />

of the improved performance will follow in 2010.<br />

References<br />

[1] M.C.Bellachioma et al., Vacuum 82 (2008), p.435-<br />

439.<br />

[2] M.C.Bellachioma et al., Proceedings of PAC09,<br />

Vancouver, BC, Canada.<br />

[3] P.Chiggiato and P.Costa Pinto, Thin Solid Film 515,<br />

(2006), p.382-388.<br />

[4] P.Chiggiato et al., unpublished, to be submitted to<br />

J.Vac.Sci.Technol. A.<br />

[5] Kollmus et al., this <strong>GSI</strong> Annual Report<br />

[5] G.Weber et al., Phys.Rev.STAB, 12, 084201 (2009).

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