Title: study of T1 relaxation time
1study of T1 relaxation time
- A proposal to test T1 using a dilution fridge and
SQUID NMA at Royal Hollow University,London
2neutron EDM temperatures, concentrations and
magnetic field
- Temperature 0.3 -0.5 K
- Relative Concentration of 3He x10-10
- Magnetic field 1 - 0.1 ?T, 32 - 3.2 Hz
-
- T1 relaxation time
- 1/T1 1/T1 Binh 1/T1bulk 1/T1wall
3Magnetic field inhomogeneities
- Relaxation of spins due to field inhomogeneities
in gaseus samples at low magnetic fields and low
pressures - G.D.Gates,S.R.Shaefer,W.Happer, PR A 37, 1988,
pp.2877 - relaxation rate at high pressure is scaled as
- That is proportional to the diffusion
constant D - In contrary, at low pressures it is inversely
proportional to the diffusion constant D
4Measurements of bulk relaxation
- Pyrex cell, Cs coating,optical pumping at room
temperature - This is a most recent result
- N.Piegay,G.Tastevin, JLTP 126 (2002)157
- Field 2 mT, 64 kHz
- cell 0.5 cc
- 3He concentrations from 0.3 to 34
- T 1.1 K
- Linear dependence on concentration
- Claim No dependence on the surface/volume ratio
- Claim relaxation rate is pure bulk effect
extrapolation to the zero concentration gives 10h - But the actual T1 measured at 0.3 were 3.5 h,
2.5 h and ? 1.5h in different cells
In this paper they do not explicitly mention how
the cells were cleaned prior to filling, however
in earlier work the cells were evacuated and
degassed above 150?C for several days before
introducing the cesium and sealing in the gas
mixture. Piegay and Tastevin say that they
present data from the three best cells. This
suggests that wall relaxation can vary. In the
paper cited for experimental detail, H2 coatings
were used with a dilute mixture and here wall
relaxation dominated, the measure total T1 being
around 400 s at 450 mK .
5Wall relaxation
- Theory predicted no substrate states for He-3
impurities - Impurity dinamics in boson quantum film,
B.E.Clements, E.Krotscheck,M.Saarela, - Phys Rev B 55 (1997),5959
- Ballistic movement of He-3 implies a very short
correlation time -gt less sensitivity to the local
fields of the wall magnetic/paramagneic
impurities - C.Lusher,PhD
6What has been measured with plastic?
- Stycast 1266
- This is a most pessimistic result
- Los Alamos group, PR B 37,N4, 1988
- Field 3T
- cylindrical cell 0.2-in r. x 0.62-in
- 3He concentrations 0.1, 0.01 and 10-3
- At 1.5 K T1 50 sec,
- no dependence on concentration
- ?-point dependence
- relaxation rate is pure wall effect that is
defined by diffusion time - ?R 2/ D
-
7What has been measured with plastic?
- Nylon cell, open geometry
- The spin diffusion Coefficient of 3He in 3He-4He
solutions - D.C. Chang and H.E. Rorschach, JLTP 10, 1973
- T1 and spin diffusion coefficient were measured
by spin-echo technique - Field 30.3 MHz, 1 T, T2100 sec
- cell volume 0.1 cc
- Gas handling system glass and stainless steel
with LHe trap for Helium sample - 3He concentrations 5 , 9 , 14 and 24
- At 0.9 K and 5 T1 25 sec,
- Below ?-point T1 is sensitive to concentration
- relaxation rate is due to wall effect defined
by diffusion time - ?R 2/ D
8Possible Experiments at Royal Holloway
Universityproposed by Chris Lusher
- We would propose to measure T1 under conditions
closer to that in the final EDM experiment. By
using DC SQUIDs we can measure T1 down to very
low magnetic fields. - The sample cell, prepared at HMI, would be
mounted on a cryostat at RHUL, allowing
measurements down to 300 mK. - We will use an open geometry with a high vacuum
gas handling system. - There are no optical pumping facilities at RHUL,
however since the DC SQUIDs are extremely
sensitive detectors of magnetic flux we can
detect lower concentrations of thermally
polarized 3He than can be obtained using
conventional NMR techniques. - We would use much higher 3He concentrations than
10-10, however in the low concentration regime
(where wall relaxation dominates over bulk
effects) the observed relaxation time is expected
to be concentration independent, since (n3B/n3W)
should be concentration independent. - It should also be relatively temperature
independent since there should be no bound state
for the 3He near the surface. - The x3 dependence should be checked since Piegay
and Tastevin say they observed some concentration
dependence of wall contributions in their
experiments. The concentration dependence could
relatively easily be measured given the open
geometry of our proposed set-up. The sensitivity
of the spectrometer is such that a signal to
noise of 1 in a single shot could be obtained at
1 K and 50 k Hz for a concentration of 10-3 for
a right circular cylinder of 10 mm length and 10
mm diameter. - Our dilution refrigerator is conventional and
therefore it is not non-magnetic. However we do
not expect field inhomogeneities to be a problem
in low fields. T2 might well be limited by
diffusion in a gradient, but the upper limit on
T2 will be T1. - We would measure the longitudinal relaxation
times as a function of frequency, temperature and
concentration in order to put a limit on the
relaxation times that could be achieved with the
deuterated plastic sample chamber in the EDM
experiment. Cryogenic coatings e.g D2 could also
be investigated.
9 Predicted sensitivity of the DC SQUID
spectrometers
- We have calculated the expected signal to noise
in a dilute solution for both a tuned and a
broadband SQUID system. The sample is considered
to be a right circular cylinder. Numbers as
follows for thermal polarizations - Broadband system at 500 kHz, concentration 10-5,
d 10 mm (right circular cylinder), T 1K,
signal to noise of 3.6 (T2)1/2 in a single shot.
Proportionally higher concentrations would be
required to go to lower magnetic
fields/frequencies. For example at 50 kHz with a
T2 of 1 ms a signal to noise of 1 would be
obtained in a single shot from x3 10-3. Since
the surface area would be made large to reduce
the observed T1 then significant improvement
could be obtained by signal averaging. - For the tuned system at 1 MHz, concentration of
10-5, d 10 mm (right circular cylinder), T
1K, a signal to noise is 38 (T2)-1/2 should be
obtained in a single shot. - We would probably use a broadband set-up in order
to measure the frequency dependence of T1.
However the possibility of looking at smaller
concentrations using a tuned spectrometer exists.
10Comparison of glass with Plastic walls
- Substrate potential is not homogeneous, surface
is rough, density is lower then glass - probably,
He-3 can be trapped? - Gases easy diffuse in at room temperature,
therefore plastic can be used only at low
temperatures, porosity and diffusion at low
temperatures- we dont know - Wall cleaning cant be baked
- can be only pumped out in vacuum
- Best result with glass is 500 sec at 0.5K, 0.5
cm3 - Nylon demonstrate 25 sec at 1K
11Open geometry and wall contamination
- Open geometry and dirty cell
- Both demonstrate a drop at ?-point
- Both demonstrate T1 ? 103 sec at 4.2K while the
clean cells usually have T1 ? 105 sec - Therefore, preliminary tests at 4.2K could be
very useful to give some ideas about quality of
the sample and cleaning procedure but real
estimation for EDM could come only from low
temperature measurement -
12Summary
- August, 2003 we can provide some samples to
TUNL. Samples can be plastic foil coated with d-
and h-coatings - September-Octobe-November - development of the
coating technic for a small cell and gas handling
system - We can do test of the chemical content (element
traces) at HMI - Magnetic susceptibility?