| |
Development has been
completed on the low-energy neutron facility which produces a series of low-energy
neutron spectra having maximum neutron energies from 40 to 110 keV, minimal
dose contributions from higher energy neutrons and g
rays, and dose rates usable for irradiation of cultured cells. The facility
is based on the 7Li(p,n)7Be reaction and uses a rotating
target design to minimize the heating of the lithium, which melts at 180°
C. Learn more about the specifications of the low-energy
neutron facility here.
There are many compelling reasons to
study slow neutrons. Some of these include:
|
Low-energy Neutron Facility
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.

Mechanistic
Rationale
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.
- 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.
-
- Boron Neutron
Capture Therapy
-
- 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.
|
|