In the final design below, the target
surface is normal to the beam direction, and the cell samples
are positioned above the beam, making placement much easier and
permitting the use of multiple samples. To enable the use of high
beam currents without melting the lithium, the target is rotated
at high speed. A beam spot 1 mm wide by 5 mm high is used to minimize
the time that the lithium is heated by the beam. The lithium is
evaporated in place in an annular ring using the port located
directly below the axis of rotation while the target is being
rotated.
The samples are positioned 2.5 cm
from the center of the beam in order to maximize the dose rates,
which are as low as 0.1 Gy/hr for the lowest-energy spectrum,
but considerably higher for the higher-energy spectra. A filter
up to 1 cm long consisting of depleted uranium, tin, copper and
aluminum is inserted between the target and the sample to reduce
the dose rate from the 477 keV gamma rays arising from the 7Li(p,p'g)7Li reaction and the characteristic X rays from the
uranium.
Dose contributions as a function
of neutron energy are presented below for the three low-energy
neutron spectra. Note that the bin widths double above 121 keV.
In the past two decades, it has
become clear that energy deposition at the nanometer level is
the prime determinant of biological effectiveness. This conclusion
has been largely based on studies using ultrasoft x-rays as a
mechanistic probe, whose secondary photoelectrons have nanometer
dimensions, However, the interpretation of these soft x-ray studies
has been strongly hampered by the non-uniform dose distribution
produced by these x rays over the range of a cellular nucleus,
due to the high attenuation coefficient of the x rays. Unlike
soft x-rays, however, low-energy neutrons produce a uniform dose
distribution across cell nuclei, thus avoiding the major problems
of dosimetry and interpretation inherent in the soft x ray approach.
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Occupational Exposure to low-energy neutrons
A significant number of people
are potentially exposed occupationally over a protracted period
to low doses of neutrons. In DOE facilities (1988 figures, Merwin
et al 1990), about 92,000 individuals were monitored as
potentially receiving neutron dose, and about 7,000 individuals
absorbed measurable neutron doses. In addition, of the approximately
600,000 monitored workers under NRC regulation, about 6,000 per
year (primarily research workers, well loggers and reactor workers)
receive measurable neutron doses (NRC, 1988 and private communication
from C. Raddatz, NRC, 1991). There is also increasing concern
about the neutron dose to which airline crew members (300,000
in U.S. airlines) are exposed. Calculations (e.g. Friedberg, 1989,
Wilson and Townsend, 1988) indicate that in some cases crew members
will receive more than the maximum permissible dose for non-radiation
workers, about half the dose equivalent coming from neutrons.
For reactor workers the neutron
energy spectrum to which occupationally exposed individuals
will be subject varies widely, even within a given reactor facility.
The neutron spectrum depends on the neutron source and on the
degree of shielding, and thus moderation, to which the neutrons
are exposed. In addition, of course, the neutrons are moderated
by the body of the exposed individual. Whether this is important
in terms of the biological effectiveness depends on whether
the neutron biological effectiveness varies significantly in
the neutron energy range of interest for occupational exposure.
The significant neutron energy
range, in terms of dose deposited, varies according to the fluence
spectrum to which the individual is exposed. The neutron energy
range from 10 to 200 keV is, however, the energy range where
there is evidence that there may be significant variations in
biological response. In the neutron energy range below ~100
keV, there are two major groups of data sets available, both
based on filtered reactor beams; these are from Sevankaev et
al (1979) in the Soviet Union (nominal 40, 90 keV) and Lloyd
and colleagues (nominal 24 keV), in the U.K. (e.g. Lloyd
et al, 1988, Morgan
et al, 1988). The yield (per unit dose at low doses)
of chromosomal aberrations in human lymphocytes, as measured
by Sevankaev et al (1979), is considerably decreased
compared with the yield at a neutron energy of a few hundred
keV. This is in accord with earlier results for cellular survival
(Hall et al, 1973)
and is also in accord with biophysical expectations (e.g. ICRU
1986, Blue et al 1995),
as well as recent ICRP recommendations (ICRP, 1991). On the
other hand, the results of the Harwell group, both for chromosomal
aberration yields in human lymphocytes, and for other end points
in rodent cells (e.g. Morgan et al 1988), suggest comparable
yields to those at a few hundred keV.
This disagreement is significant
on two levels. First, in terms of the radiation protection issues
addressed in the current proposal, a significant decrease in
the biological effectiveness of neutrons from the hundreds of
keV to the tens of keV range would result in a decrease in the
quality factor appropriate for most occupational exposure situations.
Second, in terms of biological mechanisms, radiobiological models
based on energy deposition in cellular or nucleus-sized targets
unequivocally predict a decrease in biological effect as the
neutron energy decreases; if this decrease were not to be confirmed,
then such models would be substantially falsified.
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Slow neutrons are aimed at a tumor
containing a borated drug, and neutron capture by boron causes
the emission of a highly-damaging alpha-particle in the tumor.
The limiting normal tissue damage will be produced by the soft
neutrons themselves, the biological effectiveness of which is
poorly understood.
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