Introduction to particle
accelerators and their applications - Parte II:
Components
Gabriele Chiodini
Istituto Nazionale di Fisica Nucleare
Sezione di Lecce
PhD lessons in Physics for Università del Salento
2015-16 (20 hours, 4 CFD)
The component of an accelerator
• Source
• Injection (non treated here)
• Vacuum
• Magnets
• RF
• Extraction (non treated here)
Source
Electrons
Thermionic emission Photoemission
Ions
ECR
Penning (PIG)
Negative Ions
Electron sources
• Vacuum
• Electrons emitted by a cathode
• An anode with or without a hole
• Acceleration potential
• Focusing structure
Thermionic emission
Metals heated to temperatures close to incandescence emit
Photoemission
Planck constant h=6.6E-34 J x s = 4.1E-15eV x s
The electrons of a metal can receive higher energy than vacuum energy absorbing photons ( photocathode and laser)
Metals QE=0.01% !
Semiconductor QE ~=10-30%
The accelerating structure is a RF cavity
QE=Quantum efficiency=N electrons/N photons
Quantum efficiency
QE is determined by a three step process:
!
1. Electron excitation from the valence band to conductive band
2. Electron-phonon and electron-electron scattering thermalise the electron approaching the surface
3. The electron affinity with respect to the conduction band minimum determine the probability of emission in vacuum of electron in conduction band and near the surface
! • Step 2 and 3 is less favorevol for metal than semiconductor.
• The semiconductor photocathode have high QE but low
stability in time.
Ions source
• Gas inlet
• Ionizing power input
• Plasma production region
• Magnetic confinement
• Ions extractions
Plasma
The 4th state of matter:
the plasma
• It is a rarefied and ionized gas electrically neutral (molecules, ions+, ions-, electrons).
• It screens electrically a charged object placed inside by the formation of a charge layer
• It is created by heating,
electric discharge, microwave
absorption, laser absorption
Charged particle motion in a plasma
1. Cyclotron motion along B.
Radius of tens of micron for electrons and few millimetre for ions.
2. Drift motion orthogonal to E and B equals for electrons and ions (no charge, no mass dependence).
3. Magnetic mirror or bottle (not homogeneous B push charged particles versus low field region).
ρ
girazione= qB mv
v
drift= E
B
1
2
3
ECR (Electron Cyclotron Resonace) ion source
f
girazione(elettroni) = v
2 πρ = 1 2 π
eB m
ef
girazione(elettroni) = 28B(T) = f
ECR(GHz) condizione di risonananza ECR
• The ECR plasma production region ( discharge region ) corresponds to the region where the electron cyclotron frequency is equal to the frequency of the input microwave ( resonance).
• The electrons are trapped by the magnetic mirror and heats up to keV and even to MeV energy level.
• The ions slip-out the magnetic mirror because heavier than electrons, and form the ion beam.
• No thermionic filament is used and then it is a very robust source.
ECR resonance condition
real ECR
Penning ion source or
Philips Ionization Gauge(PIG)
• Pressure = 1E-3 Atm
• B=0.1 T
• Hot or cold cathode
• Electrons are accelerated in arc discharge due to the high voltage between anode and cathode (V=1kV and I=0.1-50A )
• Electrons rotate around B (tens of micron radius) and ionise the gas very effectively before to reach the anode.
• The ions slip-out from the hole and form the
ion beam.
Real PIG real
Negative ion source
The negative ions are generated from positive ions or neutral atoms by electron transfer from substance with low electron affinity, such as an alkali metal ( for example cesium ).
Electron affinity = Energy released from electron transfer
B
Production and extraction of negative ions
NEGATIVE ION EXTRACTION
• The extraction of negative ions favours also the extraction of electrons because they have the same charge .
• By means of a dipole you can separate the electron current from the negative ion beam.
Technique 1: caesium coated cathode (surface phenomena)
Technique 2: gas+caesium
mixture(bulk phenomena)
Vacuum systems
Pressure units
The vacuum is a force: Pressure x Surface
P = nkT
Gas law n[molecules/m3]=molecular density
!
Boltzman's constant k=1.38E-23 J/K = 8.6E-5eV/K
Mass flow and Throughput
!
The quantity of gas flowing through a piping element is described by:
• Mass Flow=Mass/Time (Kg/s)
• Throughput Q = pV/Time (mbar x litre / s ) . NB 1: In a perfect gas pV=M/mkT
NB 2: The outgassing is measured in mbar x litre /s like Q
C[litres/s]=Conductance
Q=Throughput [litre x mbar / s] P1-P2=pressure drop[mbar]
Conductances in parallel increase
Conductances in series decrease C(hole area A )=11.6A[cm
2] C(tube of diameter D and length L )
=12.1D
3/L[cm
2]
It is better short and large tubes
Effective pumping speed
The pumping speed is limited by the conductance of the connecting pipe:
Example: a turbo molecular pump of 8 keuro have a pumping speed S=400 l/s.
If I connect a pipe of diameter d=10 cm and length L=2m I have C=60l/s then S
eff~60l/s.
Pumping speed of a pump
Pumping time
Q = S x p
Vdp/dt = S x p dp/dt = S x p / V dp/dt/p=S/V
In a vacuum tight volume V at pressure p without gas leak the pumping time is determined by the
where S is the effective pumping speed
The pressure follow the exponential decay law with time
constant = S/V
Viscous and molecular flow
λ
aria[cm] ~ 6.7 ⋅10
−3P[mbar]
1 < P < 10
3mbar 6.7 ⋅10
−6< λ
aria< 6.7 ⋅10
−3cm
10
−3< P < 1 mbar 6.7 ⋅10
−3< λ
aria< 6.7 cm
P < 10
−3mbar 6.7 cm < λ
ariaMolecular flux: dominated by collisions with the wall Viscous flux: dominated by intra-molecule collisions Molecular mean free path in air
• The two regimes differ each other completely for calculations and vacuum components.
• The molecular regime is the true vacuum technology and is dominated by the nature of the surface
walls which continuously release molecules ( Outgassing )
Vacuum classification
• Medium vacuum: 10 -3 <P<1mbar
viscous flux
• High vacuum: 10 -7 <P<10 -3 mbar
molecular flux
• Ultra high vaccum: 10 -12 <P<10 -7 mbar
molecular flux
Outgassing and cleaning
• In a vacuum system the final pressure is given by the OUTGASSING of the surface walls.
• The outgassing depends on the nature, treatment, cleaning, temperature and pumping time
• Methods of cleaning
• Remove residues by chemical products
• Fire under vacuum at 9500C to extract hydrogen from stainless steel
• Electrical discharges to remove gas and atomic metal
• Heating to 1500C to remove water molecules ( bake- out )
P finale = Q outgas sin g
S eff
Use ONLY metals NEVER plastics:
Q plastics =5000Q metals
Metals vs Plastics
P
finale= Q
outgas sin gS
eff= q
outgas sin gA
S
effVacuum measurements 1:
1E-4mbar<P<1 mbar
PIRANI GAUGE
below 1E-4mbar gives wrong values The reading is done by zeroing a resistive bridge by
setting the current value necessary to maintain constant
the temperature of a THERMISTOR placed in vacuum .
Lower is the pressure, less cooling on the thermistor
and less current is needed to keep it warm.
Vacuum measurements 2:
1E-10mbar<P<1E-5 mbar
PENNING GAUGE
M e a s u r e t h e
discharge current of
a P e n n i n g c e l l
b e t w e e n c o l d
cathode and cold
anode in magnetic
field.
Vacuum measurements 3:
1E-12mbar<P<1E-5 mbar
BAYARD-ALPERT GAUGE
Measure the current of the electrons emitted in
vacuum from a hot filament and rotating in a
magnetic field
Pumps to create the vacuum
Primary rotational pump ( dry or oil ) used to pump from environmental pressure to 1E - 2 mbar . S = m3 / h .
It works in viscous regime creating a pressure drop between input and output .
Often it prepares the vacuum for the turbomolecular pump.
Pumps to create the vacuum
Turbo-molecular pump used to pump from 1E-2 mbar up to 1E-11mbar and then it can be removed. S = 10 to 3000 l / s .
It works in molecular regime by
momentum transfer: when a
molecule touches the blades
rotating at a very high speed
comparable to the molecule
thermal speed the molecule is
removed from the volume .
Pumps to keep the vacuum
!
Ion sputtering pump is used to maintain the vacuum and can work from 1E- 5 mbar up to 1E-11mbar. S = 1-500 l/s .
It is a Penning cell where the emitted electrons ( 6kV ) ionize residual molecules and sputter the titanium covering the cathode.
The sputtered titanium can
chemically bond the residual
gases or bury the not reactive
o n e ( n o b l e g a s e s a n d
hydrocarbons ) carrying them
on the metal walls where they
Vacuum components
Below
Cooper pipe
Collar,gasket, L-pipe Flange
Secti on va lves
Normal conductive
magnets
Magnet components
Normal conductive magnet
• PRO IRON
• Less Ampere x Nturn
• Less dissipated power
• Guide and shape the magnetic field
• CONV IRON
• Saturate at about 2 Tesla (all magnetic domains are oriented along B)
B
traferro= µ
0NI
h = B
NI(1 + χ
ferro)
Microscopic currents (oriented magnetic domain)
The standard coil is made by rectangular wires of copper or Coil
aluminium with cooling water going through.
The wires are isolated and glued together by glass and epoxy resin.
2 Layers
4 Layers
• Maximise NI (Ampere x turn)
• Choose conductor area A and number of turn N
• Current density J= NI/A
Many N: low current (less losses), small terminal (easy and cheap connection), more isolation, more assembly cost, higher voltage
Low J : less losses, less consumption, less cooling
The limit of the normal conductive magnets
The iron saturates at T = 1.5 -1.8T and in ramping regime as in a synchrotrons can not exceed a magnetic field of 1-1.2T .
!
You need to switch to the superconducting magnets (zero electric resistance) which are free of iron, but just coils with very high currents (10,000 A) and no power dissipation.
!
But the superconductive magnet coil must be kept at
temperatures close to absolute zero and therefore require
cryogenics cooling systems.
Comparison normal and super conductive magnets
T=4.2K At LHC (Large Hadron Collider) all the magnets are made of NbTi superconductive and cooled
down to less than 2 K.
!
The cryogenic fluid at LHC is the superfluid He II (PERFECT HEAT CONDUCTOR):
• zero viscosity
• second sound (heat waves)
Radio-Frequency
accelerating structure
What is a RF system
• A charged particle could be accelerated only electric field parallel to the direction of motion
• Variable fields can increase energy without voltage built-up
• Wideroe’s drift tube can work only at low frequency because at high frequency the drift tube are not anymoe equipotential:
• low energy
• low filed gradient
It is necessary to abandon drift tubes with uniform fields
for accelerating structures with distributed fields
Electromagnetic
spectrum
Dispersion relation in a pipe
Vacuum Cylindrical
pipe
Waveguide
Dispersion relation in a RF cavity
RF cavity
Waveguide with
obstacles
Main RF components
• RF oscillator
• RF power amplifier
• Coupling amplifier-cavity
• Accelerating cavity
• IN and OUT beam
• IN and OUT RF wave
• Power meter (Antenna)
Disk-loaded guide waves with traveling waves (TW)
Guide wave IRIS-loaded:
• f=2.856 GHz (S band)
• 86 acceleration cells
• Coupling input/output
• Accelerating file 30 MV/m
Wave guide allows to create a
longitudinal component to the
electromagnetic field and the
discs to reduce the wave
phase velocity less than the
velocity of light in vacuum in
such a way it can accelerate
RF resonator with standing wave (SW)
Reentrant Nose-cone Disk-loaded Coaxial
The resonant cavities are characterised by stationary resonant modes that oscillate in time with frequency f and in the space with a wavelength λ without propagate ( Standing Wave ) . The standing wave is the sum of two waves traveling in the opposite direction and completely interfering at the boundaries.
V
viaggiante(x, t) = V
0sin(2πft − 2π λ x) V
stazionaria(x, t) = V
0sin(2πft)sin( 2π λ x)
Traveling wave Standing wave
The boundary conditions
decide if TW o SW
Figure of merit of a RF cavity
• E=Accelerating field =V/L (Inside the Cavity)
• Q=Total Energy/ Dissipated Energy =U/P=f
0/Δf
• Dissipated energy P due to surface resistivity of the RF conductor wall at high frequency (skin effect) = V x I = V
2/R = I
2R (In Cavity Wall).
R can be drastically reduce by a super-conducing RF cavity (Rs=8nΩ one million time lower than
0