ACCELERATOR VACUUM PROBLEMS: IN-LINE OIL TRAPPING BETWEgN THE STANFORD LINEAR ACCELERATOR AND THE BEAM SWITCHYARD

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slac-pub-75 March 1965 ACCELERATOR VACUUM PROBLEMS: IN-LINE OIL TRAPPING BETWEgN THE STANFORD LINEAR ACCELERATOR AND THE BEAM SWITCHYARD E. L. Hoyt and E. L. Garwin Stanford Linear Accelerator Center Stanford University, Stanford,,California Summary The thirty accelerator sectors (each 330 feet long) of the two-mile machine will be evacuated with sputter-ion pumps to pressures 1~:: enounh to limit rf breakdown and multipact r problems. hfter the bt-aleaves the xcelerator 3. will be ",-jitched" by pulsed magnets to one or more of the axprimental areas through the looo-foot beam switchyard. Due to the nature of the equipment in the beam switchyard and the requirements for inexpensive, non-elastomeric, remotely operable couplings, there will be a high probability for virtual and real leaks and a consequent need for continuous high throughput pumping. Oil diffusion pumps are therefore used to evacuate the four branching beam tubes of the beam switchyard. Some kind of in-line oil trap is needed to separate the clean, low pressure (10e7 torr), ionpumped accelerator from the oil-pumped (lo-" torr) beam switchyard end of the machine. This trap should limit the amount of oil and organic fractions passing back through to the accelerator and should provide some of the impedance necessary to obtain the three-order-of-magnitude pressure difference between accelerator and switchyard. The pressure differe,ice will be maintained by differentially pumping on each of two in-line vacuum impedances. One of these impedances will be a standard lo-foot section of disk-loaded waveguide and will act as an oil trap. When refrigerated, such a trap had measured transmission probabilities of 10-g to 10-s for heavy hydrocarbons. Test Setup and Procedure Figure 1 is a photograph of a standard lo-foot waveguide with longitudinal cooling tubes. Figure 2 shows a cutaway section of the disk-loaded waveguide. Figure 3 shows the test setup. The idea was to simulate the anticipated pressure and gas throughput conditions of the differential pumping system and to measure the amount of oil or hydroisy-oon fractions that traversed the waveguide when it was refrigerated and oil was purposely introduced at the diffusion pump end. DC 705 Oil The tests were conducted with Dow Corning 705 diffusion pump oil. Chemically, DC 705 is pentaphenyl trimethyl trisiloxane with a molecular weight of 546 and a specific gravity at 25'C of 1.095 g/cc. The vapor pressure of DC 705 follows the simple relation: ~~12.31 and B=6490 which gives a vapor pressure of < lo-' torr at 25OC and = 1 torr at 25oOc. The diffusion pump and both oil effusion cells were loaded with DC 705 oil.. Mass Spectrometer A Consolidated Electrodynamics Corporation Type 21-613 residual gas analyzer was the principal tooi employed to measure the partial pressures of the gases reaching the -- ion-pumped end of the test section. Tne instrument was calibrated with nitrogen and found to have a sensitivity of 4 X lo-l1 torr/division for this gas. On the basis of other work showing sensitivities for most other gases not different by more than a factor of 2, we assumed a sensitivity of 4 x lo-ii torr/scale division for all gases commonly measured except hjjdrcgen and helium. The mass spectrometer, connecting tubes, and the chamber at the ion-pump end were all held at temperatures of 80-100~~: dzing the tests. This ensured that any oil entering this region would be at a high enough vapor pressure to be readily detected with the mass spectrometer. Test Sequence Complete mass spectra patterns were recorded intermittently during all phases of the tests. Altogether over 100 pat.terns covering the mass range 2 to 400 were obtained during the following test sequence: 1. Ion pumping only. 2. Diffusion pius ion pumping. 3. Before and after baking system. 4. Following refrigeration ofwaveguideto-37'c. 5. Following heating of transverse injection oil cell to > 2OOOC (vapor pressure approtimately 80 microns). 6. Following introduction of nitrogen through x Work supported by U. S. Atomic Energy Commission (Submitted to IEEE Particle Acceierator Conference, Washington, D.C., March 10-12, 1965)

_-- -- - I leak valve to simulate gas load in switchyard and flow toward ion pump end. 7. Following heating of axial injection oil cell to 250~~ (vapor pressure approximately 1 torr). 8. Following admission of viscous flow pressure waves sent down waveguide by ra_oidly opening the nitrogen leak valve at the diffusion pump end. _ 9. Pllowing cut-off of refrigpratic- al,d r?- turn of pipe to room temper9ure. how long it might take to cover the internal parts of the accelerator with a monolayer of organic molecules. time to form monolayer = number of sites rate of arrival x sticking fraction r'-om -ler':: 7~11 diffraction work we can assume mon.,l aye cc le;-st:: r-e-iuil-es 2 X 1014 molecules/cm2 for rrml~c~~.~-s of average mass 100. 10. Following heating of waveguide and ion puml: end in effort to drive back hydrocarbons. 11. Following re-refrigeration of waveguide to -37Oc. Results Figure 4 shows the changes in the sum;ned partial pressures of the heavy hydrocarbon groups (all masses > 44) as changes were made ill the test conditions. It can be seen that any sudden change in pressure drove additional hydrocarbons through the trap. However, even under the most severe condition tested, the hydrocarbon pressure ratio from one end to the other of the refrigerated "trap" was of the order of 106, while under steady-state conditions, the ratio was 10' or greater. From the test results we can make some estimate of how much oil and/or organic fractions might get through the "trap" under the worst anticipated conditions. For this analysis, let us assume a steady-state transmission rate for heavy organics, corresponding to a partial pressure, during the tests, of 10 -lo torr. Transmission rate = pumping speed X partial pressure Speed for mass 58 measured at the spectrometer was 20 liters/set. Therefore, liters transmission rate = 20 set X 10-i' torr For this argument, we assume that the sticking probability for heavy organics is 1.0. Therefore the minimum time required to get a monolayer on 1 cm2 would be: 2 x 1014 6.6 x lo'" = 3000 seconds The inte,nal area of the last ten-foot section of the accelerator with related waveguide and vacuum plumbing is approximately lo5 cm2. Therefore, monolayer coverage of this part would take 3 x 10' seconds or nearly 10 years. Conclusions It has been demonstrated that a refrigerated disk-loaded waveguide section can act as an effective barrier and reduce to low values (< 1O'i molecules/sec) the number of heavy hydrocarbon molecules reaching the accelerator from the beam switchyard and the end stations where oil pumps will be used. For noncondensable gases in the molecular-flow regime, pressure ratios of 100 to 300 can easily be maintained across the disk-loaded waveguide. The waveguide will be maintained sufficiently 3ut of tune to prevent significant absorption of rf power from the beam. Heating the "trap" in order to drive back the accumulated oil and oil fractions did not appear promising. Therefore, great care will be taken to ensure that the trap remains cold, or valved-off when permitted to warm up. -._ =2x10-9 torr-liter set Converting to molecules, we get 2 x 10-9 torr-liter x 3.3 x 101s molecules see torr-liter = lo molecules 6.6 x 10 set From this transmission rate, we can estimate

_-- -- FIG. l--standard lo-foot accelerator section (disk-loaded wave&de).

I - -- - -_ -. %

/ ION GAGE RESIDUAL GAS ANALYZER DEWAR-, I uuuuuuuuuuuuuuuuuuuuuuuuu~ nnnnnnnnnnnnn_nnnnnnnnnu ~~73!!!!!2~ ION L VALVE THERMOCOUPLES -J\ L\ I OIL CELL-TRAN3 1EFtSE FIG, 3 - TEST SETUP USING IO FT. ACCELERATOR SECTION AS AN OIL BARRIER 130-I-A

I I I I I 1 I I I I I I FOLLOWING CUT-OFF---, OF REFRIGERATION BEGIN REFRIGERATION : ~ T a~ns%%$~ll CELL FOLLOWING VISCOUS FLOW PRESSURE BURSTS \ BEGIN ON-AXIS HEATING OIL L 0 4 B 12 I6 20 24 28 32 TIME - MINUTES X10 \ - 36 40 44 48 52 FIG.4 - PARTIAL PRESSURE OF HEAVY HYDROCARBONS MEASURED AT MASS SPECTROMETER DURING OIL TRAPPING TESTS 130-2-A