Neutron Physics - MIT

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Neutron PhysicsMIT Department of Physics(Dated: October 16, 2014)The technique of time-of-flight spectroscopy with a mechanical beam chopper is used to study theproperties of thermal neutrons in a beam emerging from the MIT Research Reactor (MITR-II) at theMIT Nuclear Reactor Laboratory. First, the distribution in velocity of the neutrons is measured,and the results are compared with the Maxwell-Boltzmann distribution for the temperature ofthe reactor. Second, the De Broglie relation between wavelength and momentum of neutrons isdetermined from measurements of the angle of Bragg reflection of the beam from a copper crystal asa function of the velocity measured by time-of-flight. Third, the absorption cross sections of severalelements are measured, and the 1/v dependence of the boron cross section is observed.PREPARATORY QUESTIONSPlease visit the Neutron Physics chapter on the 8.13xwebsite at mitx.mit.edu to review the background material for this experiment. Answer all questions found inthe chapter. Work out the solutions in your laboratorynotebook; submit your answers on the web site.SAFETYthe experiment remotely from Junior Lab. Any time youneed to visit the experiment in the reactor containmentbuilding, you must be escorted by an authorized JuniorLab staff member or NRL personnel. NRL protocolsrequire that you wear long pants and closed-toeshoes without pointed heels whenever visiting thefacility.For the purpose of Junior Laboratory experimentation,the following steps should be taken in order to have accessto the reactor:Training Requirements1. First, complete the trainings described in the Neutron Spectrometer Operation Manual.The following must be completed before starting theexperiment:2. Entry into the NRL building is through a lockeddoor on Albany Street which may be opened withan authorized MIT ID, or by ringing the doorbell.1. Peruse the MIT NRL website and familiarize yourself with the reactor setup and experimental facilities: http://web.mit.edu/nrl/www/index.html.2. Read through the Neutron Spectrometer OperationsManual, which is posted in the Materials section ofthe course’s Stellar website. Note, this document isprotected for class-only access, and should not beshared outside MIT.3. Radiation Safety: Reactor training (web-based,EHS00311w). This may take up to two hours, andcan be done from any computer with MIT personalcertificates installed. Instructions can be found inthe Neutron Spectrometer Operation Manual.Experimentation at the MIT Research Reactor:Radiation Protection, Access, and SecurityAs with all nuclear reactor facilities in the UnitedStates, access to the reactor building is restricted in accordance with federal regulations administered by the USNuclear Regulatory Commission. You will be required tocomplete radiation safety training and be escorted at alltimes.In keeping with the spirit of the Junior Lab, you willoperate all the equipment yourself during the first labsession at the reactor. After that, you will be able to run3. Entry procedures for the reactor containmentbuilding will be described during the practicumtour. All access to the containment building andthe experiment is restricted. You must be accompanied by an authorized escort.4. For your first scheduled lab period, begin by meeting your lab partner at Junior Lab. An instructoror technical staff member will then take you to theNRL and show you the apparatus and procedures.Please contact Junior Lab staff (extensions x3-5082or x2-2122) in advance if a conflict or change ofschedule interferes with this important introductory session.5. The equipment is reserved for your use at thescheduled lab time. To operate the experiment remotely you must remotely access the experimentcomputer. Instructions can be found in the Neutron Spectrometer Operation Manual. You shouldrequest any proposed changes to your scheduled attendance with your section instructor.SUGGESTED SCHEDULEBy the end of the second session, you should calculatethe velocity of the particles to zeroth order using MCSId: 38.neutrons.tex,v 1.97 2014/10/16 15:00:40 spatrick Exp

Id: 38.neutrons.tex,v 1.97 2014/10/16 15:00:40 spatrick Expdistributions of neutron time of flights at the near andfar detector positions.2values, you will find for the nuclear masses of the entriesin the first reaction:M (23592 U) 235.11240I.M (8735 Br) 86.95722INTRODUCTIONThis experiment was developed for Junior Lab by Professor Clifford Shull [1]. It employs a rather intense beamof low energy neutrons produced at the MIT ResearchReactor (MITR-II) located in Building NW12 on theedge of the campus at 138 Albany Street. The MIT reactor has been operating since 1958 and has served as abase for countless investigations by faculty, graduate andundergraduate thesis students, UROP and other undergraduate student projects. Use of its facilities is perfectlysafe, providing reasonable and common-sense guidelinesand procedures are followed. These guidelines and procedures are covered in the training you are instructed tocomplete in the Neutron Spectrometer Operation Manual.The three main parts of the experiment are: theMaxwell-Boltzmann distribution, Bragg scattering ofthermalized neutrons and the De Broglie relation, andfinally neutron absorption cross sections.I.1.Operational Physics of a Nuclear ReactorThe nuclear reactor is a chain-reacting system whichbears resemblance in operational principle to a coal fire,with nuclear reactions being the source of heat ratherthan chemical reactions. In a coal fire, some carbonatoms are excited by thermal “starting” so that theycombine with oxygen (burn). The heat released inthis exothermic chemical reaction activates other carbonatoms to do the same, thereby forming a chain reactionwithout further need of starting. The fire grows in intensity until an equilibrium level is reached, wherein heatlosses from the system limit the thermal power availablefor further steps in the chain reacting process.In a nuclear reactor, the counterpart to the carbon fuelis the nuclear fuel (most commonly the fissionable isotope of uranium, 23592 U), and neutrons serve as the communicative thermal energy counterpart. In 1939 Hahnand Strassman discovered that neutrons react with uranium nuclei to cause fission in which the heavy nucleussplits into two smaller and not necessarily equal nucleiplus “debris” such as neutrons, gamma-rays, electrons,etc. The fragmentation can proceed in many differentways. Typical reactions are shown in Equation 1.10n871481 23592 U 35 Br 57 La 0 n 9436Kr 13956Ba 310 n(1a)(1b)Notice that the above reaction equations are writtenas balanced equations in both numbers of nucleons andcharge. However, if you look in a table of precise massM (14857 La) 147.98930These values imply a mass loss of 0.16588 mass unitsin the reaction. Using the Einstein mass-energy equivalence, this calculates to 155 MeV of energy which, according to the energy conservation principle, must show up askinetic energy distributed among the reaction fragments.This is a very large amount of energy when comparedwith that of ordinary nuclear processes such as alpha,beta or gamma decay (1–10 MeV), and especially whencompared to chemical reactions ( 5 eV).A second notable feature of fission reactions is thatneutrons are released as debris. Shortly after the discovery of fission, careful measurements in several laboratories proved that the average number of neutrons released per fission is more than one. It was then apparent that under appropriate circumstances these neutronscould initiate fission of other 23592 U nuclei and that thephysical basis for a nuclear chain reaction exists. Thepossibilities for practical nuclear power generation andfor weapons were immediately recognized by experts allover the world, and a race began. The first controllednuclear chain reaction was achieved in 1941 at the University of Chicago by a team under the direction of EnricoFermi, and the first bomb was exploded in 1945.Nuclide23392 U23592 U23994 Puνηtherm ηfast2.50 2.27 2.602.43 2.06 2.182.90 2.10 2.74TABLE I. Number of neutrons liberated per neutron capturein fissile material. In the table, ν is the neutrons liberated perthermal neutron induced fission, ηtherm is the neutrons liberated per thermal neutron absorbed, and ηfast is the neutronsliberated per fast neutron absorbed.Table I lists the average numbers of neutrons releasedin various fissile materials. In this table, the differencesbetween ν and η (defined therein) arises because neutronsare sometimes captured without producing fission.For technical reasons of efficiency and control, most nuclear reacting systems operate so that the neutrons whichproduce the fissioning are “slow”, i.e. have very low kinetic energy. On the other hand, the neutrons whichare released in the fission process are “fast” neutronswith relatively high kinetic energy, on the average about1.5 MeV. Thus they must be slowed down (or moderated)to a low energy. This can be done by elastic scattering ofthe neutrons from light atoms in a cool moderator. Eachscattering reduces the energy of a neutron until its energyapproaches the mean energy of the moderator atoms in

Id: 38.neutrons.tex,v 1.97 2014/10/16 15:00:40 spatrick ExpFission Cross Section for U235Nuclide Fission Capture Capture/Fission(barns) (barns)ratio23290 Th23392 U23592 U23892 U23994 Pu310Cross Section 20.184—0.387TABLE II. Thermal neutron cross-sections for nuclear materials.110I.2.0Design Features of a Nuclear Reactor10 210010210Neutron Energy (eV)4610FIG. 1. Schematic fission cross-section foratom.kaeri.re.kr/ton.1023592 U.Data fromaccordance with the equipartition theorem of statisticalphysics. Carbon in the form of graphite was used as themoderator in Fermi’s first reactor. Light water (H2 O) isnow commonly used (as in the MIT reactor). Analysisshows that, on the average, one needs about 18 scattering events with hydrogen nuclei (protons) to reduce theneutron energy from 1.5 MeV to a typical thermal energyof 1/40 eV at which point further scattering events canraise as well as lower the neutron energy. The thermalequilibrium is characterized by the physical temperatureof the moderator (about 50 C at MIT, but much higherin a power-producing reactor).The efficiency of neutrons in producing fission depends upon the neutron energy and is conventionallydescribed in terms of the fission cross section, or effective target area of the fissioning nucleus, expressed inbarns (a picturesque name for 10 24 cm2 ). The dependence of this upon neutron energy for the case of 23592 Uis shown in Figure 1 which displays a nice distinctionbetween commonly-designated neutron groups: slow orthermal ( 0.1 eV), resonance (0.1–1000 eV), and fast( 10, 000 eV). Note particularly the much higher fissioncross section for thermal neutrons. Neutron physics issometimes studied in regimes beyond the above classes,in particular as cold or ultra-cold ( 10 7 eV). Ultra-coldneutrons (UCN) exhibit very interesting properties. Forexample, in a life-time measurement of UCN it was foundthat they cannot penetrate surfaces and can be containedin an experimental “bottle”!An important quantity for reactor design purposes isthe fission cross section at the thermal energy which isattained by most of the neutrons after moderation. For amoderator kept at temperature T (absolute Kelvin), thethermal energy is kT and at room temperature this isabout 1/40 eV. The cross sections for fissionable nucleiare listed in Table II.In the preceding section, we have surveyed some ofthe physical concepts and parameters that are of significance in thinking about a nuclear chain reaction. Ofcourse, this is far removed from answering the question,“how to make it work?”. Many different reactor designshave evolved, each one aimed at achieving certain objectives. Research reactors produce radiation, radionuclides or other products useful in scientific and medicalstudies; power reactors produce energy for practical use;production reactors use excess neutrons to transmute theabundant non-fissionable isotope of uranium, 23892 U, intofissionable plutonium, 23994 Pu for weapons.Components of a reactor that are common to all designs include:Fuel Elements: Either natural uranium or uranium enriched in the isotope 23592 U, usually in the form ofuranium oxide or alloyed with aluminum and sealedin aluminum tubes or plates.Moderator: Frequently light or heavy water, but insome cases graphite or beryllium.Thermal Heat Transfer System: Removes the heatgenerated by conversion of the kinetic energy of thefission fragments. The latter are entirely retainedin the fuel elements.Control Elements: Neutron absorbing elements suchas cadmium are used to control the neutron fluxdensity and hence the rate of the chain reactionand power output of the reactor.Surrounding Radiation Shield: Intense neutron andgamma radiation, produced by the fission processand the radioactive decay of fission fragments, mustbe contained by shielding.The simplest spatial configuration of these componentswould be many small fuel elements positioned in a spatiallattice and immersed in a liquid moderator which is circulated through an external heat exchanger to dissipateor utilize the heat generated by the process. To maintainthe desired power level thermometers and/or radiation

Id: 38.neutrons.tex,v 1.97 2014/10/16 15:00:40 spatrick Expmonitors would be connected to servo-mechanisms to adjust automatically the positions of cadmium control rodsinserted into the lattice. Details of the particular featuresof the MITR-II will be provided to you at the time of yourpracticum. Useful references on nuclear engineering andreactors include [2–4].I.3.Bragg Diffraction of Neutrons and theDe Broglie RelationSee Bragg (1915) [5].In the early years of the twentieth century, physicistswere faced with the wave-particle dilemma in describingthe properties of the electromagnetic field and how it interacts with matter. Young’s interference experimentswith visible light (1801), Hertz’s experiments with radiowaves (1887), and von Laue’s discovery of x-ray diffraction (1912) showed wave interference and provided measures of wavelength for electromagnetic radiation fromradio to x rays. On the other hand, Planck’s theory of theblack-body spectrum (1901), and Einstein’s theory of thephotoelectric effect (1905) showed that electromagneticradiation is absorbed at a surface in discrete amounts ofenergy (quanta) and not as a continuous flow. Bohr’stheory of the hydrogen atom (1913) showed that electromagnetic energy is emitted in discrete quanta. And,finally, Compton’s interpretation of his own experimentson the incoherent scattering of x rays (1923) showed thatx rays of wavelength λ interact with free electrons likeparticles with energy hc/λ and momentum h/λ. A composite picture was thus formed in which electromagneticradiation is characterized by the seemingly contradictoryconcepts of wave frequency and wavelength, and particlemomentum and energy.Recognizing this interrelation for photons betweenwave and dynamical properties, De Broglie suggested in1924 (in his PhD thesis) that similar properties shouldcharacterize all particles of matter. At that period, matter was considered to be made up of electrons and protons. This meant that electrons and protons (or anycomposite of them like an atom, a baseball, or the Earth)in motion should possess a wave character. De Broglieproposed a relation between the wavelength λ and momentum mv:hλ ,(2)mvwhere h is Planck’s constant. This relation is the same asfor photons, with, however, the recognition that photonmomentum obeys p E/c (with the photon energy E hν and ν the electromagnetic wave frequency).Although not taken too seriously at first — it is reported that Einstein himself was incredulous initially —De Broglie’s suggestion was given full acceptance withthe discovery of electron diffraction by G. P. Thompson and by Davison and Germer in 1927. They drewupon the fact that atoms in a crystal are positioned relative to each other in a very regular way, and that their4spacing is a few Angstroms (1Å 10 10 m) in scale.Their experiments on the reflection of electron beamsfrom metal crystals demonstrated that wave interferenceeffects were obtained with electrons of an energy suchthat their De Broglie wavelength is comparable to theseparation of the crystal planes, a result completely analogous to that previously observed with x-ray photons(which certainly were endowed with a wavelength) andinterpreted by Laue and Bragg. Since that time, furtherconfirmation of the wave-particle duality has come forother types of particles (waves) such as alpha particles,atoms, neutrons and mesons. We shall see this dualityin full display in Section I.3 of this experiment, wherewe shall again directly measure the velocity of a groupof neutrons and at the same time observe the diffractionof these same neutrons by a crystal, thereby establishingtheir De Broglie wavelength.II.II.1.THEORYThermal Spectrum TheoryThe Maxwell-Boltzmann distribution law describes thedistribution in speed (or kinetic energy or momentum) ofatoms in a gas in a state of thermal equilibrium. Neutrons within the reactor can be expected to obey a similardistribution law, namely 2 4N v 2vn(v)dv exp 2 dv,(3)v0π v03where v is the neutron speed, v0 is the most probablespeed (i.e. the peak of the speed spectrum), N is volumedensity of all neutrons (i.e. neutrons/volume), n(v)dv isthe neutron density for those with speeds falling in thespeed interval between v and v dv. (See texts on gaskinetic theory, e.g. Reference [6, 7].)This can be recast in terms of other kinetic parameterssuch as kinetic energy E for which we have1E mv 2anddE mvdv,(4)2yielding 1/2 EEn(E)dE exp dE,(5)E0E0with1mv 2 kT,(6)2 0where m is the neutron mass.The corresponding flux density in the collimated beam,i.e. the number of neutrons per unit area per unit timewith velocity between v and v dv passing a given point,isE0 j(v)dv vn(v)dv 2 v J0 v exp 2 dv.v03(7)

Id: 38.neutrons.tex,v 1.97 2014/10/16 15:00:40 spatrick ExpAs mentioned above, the neutron detector is a “thin”counter for which the efficiency e varies with neutronspeed as 1/v. Thuse A(1/v),B(8)with A being some constant. If we now call j 0 (v)dv thenumber of detected neutrons per unit area of detector perunit time with velocity between v and v dv, then 2 v(9)j 0 (v)dv Bv 2 exp 2 dv,v0where B is a constant. Can you figure out the reason forusing a “thin” counter rather than using one with higherefficiency of say 50%, aside from the fact that we don’tneed the higher efficiency because the measured intensityis adequately high?In the experiment you will perform, the quantity actually measured by the apparatus in each event is not thevelocity, but rather the time interval between a fiducial“start” signal from a photodetector and the detection ofa neutron by a BF3 detector. The accumulated data isthen the number Ni of neutrons detected in the ith timechannel, corresponding, after appropriate calibration andzero-time correction, to a flight time ti . Since L vt,we have 1L2Ni D 4 exp 2 2 t,(10)tiv0 t iwhere t is the finite and constant width of a the timechannels, ti is a flight time within the ith interval, and Dis a constant.Note that 2 2L1ln(t4i Ni ) constant,(11)v0tior, equivalently, that Niv2 Q i2 ,ln4viv0(12)where Q is a constant. Thus a display of the quantity(Ni /vi4 ) against vi2 on semi-log scale should be a straightline with negative slope (1/v02 ). It will be convenient todisplay the data in this way to check the validity of theMaxwell-Boltzmann distribution and to evaluate v0 andT.II.2.BBragg Diffraction of Neutrons and theDe Broglie RelationWe shall require some facts about crystals and thewave interference effects that may be observed withthem. As mentioned above, a crystal represents a collection of many atoms bound together by inter-atomicforces to form a three-dimensional solid. (However, twodimensional cases and liquid crystals are known to exist.)5atomplanethree-dimensional crystalFIG. 2. Schematic representation of a crystal with rows ofatoms extending into the page.θΒλθΒatomplaneσFIG. 3. Schematic representation of a diffraction grating as aone-dimensional set of scattering centers.In a perfect crystal, the atoms are positioned in a spatialarray (or lattice) with precision, this being determinedby the symmetry and balancing of inter-atomic forces oneach atom. With this regularity of position, illustratedschematically in Figure 2, it is easy to envision the overallcrystal as being made up of parallel sheets (or planes) ofatoms which can serve to provide wave interference between the components of radiation scattered by individual atoms. Almost any textbook on modern physics (e.g.,reference [8, 9]) will have an elementary derivation of theconditions necessary for constructive interference of radiation scattered from atoms in a crystal plane. Theseconditions are expressed by Bragg’s law,nλ 2d sin θB ,(13)where n {1, 2, 3, . . .} is the order of diffraction, λ isthe wavelength, d is the interplanar spacing, and θB ,called the Bragg angle, is the grazing angle of incidenceand reflection. It is deceptively similar in appearance tothe law describing constructive interference from a onedimensional set of scattering centers (e.g. a grating), andit is worth pointing out the difference.In the one-dimensional case, illustrated in Figure 3,the approach angle θ1 may have any value, and the exiting angle θ2 for constructive interference is then defined by the interference equation with θ2 not necessarilyequal to θ1 . For reasons not so obvious, this generality is not present in three-dimensional diffraction whereθ1 θ2 θB . In fact, diffraction from a crystal al-

Id: 38.neutrons.tex,v 1.97 2014/10/16 15:00:40 spatrick caaface-centeredcubicFIG. 4. The three forms of cubic crystals.ways occurs in symmetrical fashion from atom planeswith both incident and emergent angles being equal toθB . (This subtle distinction is discussed in [10] and invarious texts on crystallography, e.g. X-Ray Crystallography, M. Wolfson, Cambridge 1970.) A given set ofatom planes of spacing d will reflect radiation of wavelength λ with intensity concentrated in a narrow range ofangles (typically within 10 5 radians) with a maximumat the Bragg angle θB defined above. This is not truefor the one-dimensional grating where, for any incidentangle θ1 , diffraction maxima occur at angles θ2 given bythe formula in the figure, provided d λ.II.3.-X-Yaaa6CrystallographyA crystal may be considered as being made up of aninfinite number of different atom plane layers, each setwith a different interplanar spacing and different orientation. Bragg diffraction can occur from any of thesesets as long as the Bragg law is satisfied. What we needat this point is a shorthand method of classifying thesedifferent sets of planes, which we now develop. Sincenature causes atoms to pack together in different ways(but always in a given way for a given species of atomsor molecules; a change of external conditions such as thetemperature, pressure, or magnetic field application caninvoke a change of structure, a phase transition), it isapparent that many different forms of crystal structuremay be encountered. These are classified according tosymmetry characteristics: cubic, hexagonal, orthorhombic, etc. Common to all forms is the concept of the unitcell which represents the smallest collection of atoms (ormolecules) which, when repeated along the three axes,make up the whole crystal. Thus cubic crystals have cubic unit cells and the size of the unit cell a0 is set by onedimension. However, cubic cells may contain any one ofthree different atom configurations as shown in Figure 4.For the general case, the unit cell can be defined bythree vectors a, b, and c directed parallel to the unitcell edges and of magnitude equal to the size in thatdirection. Furthermore, we can identify the orientationof any plane of atoms in the crystal by the intersectionsof this plane with the three axes of the unit cell. It is agreat convenience to do this in terms of the Miller indicesh, k, and l (small integers) with a/h, b/k, c/l being theintersection points of the plane with the respective axes,Xahbkca bY(100)ca b-Z(112)ca b(200)cba(111)ca b(110)FIG. 5. Diagrams showing how Miller indices are used todefine crystal planes.as illustrated in Figure 5.We label a particular set of atomic planes as being(hkl) planes according to these Miller indices. A littlegeometry will show, for the case of a cubic crystal, thatthe interplanar spacing dhkl will be given simply bydhkl a0.(h2 k 2 l2 )1/2(14)In our experiment, we shall be using a metal crystalof pure copper which has a face centered cubic structure (four unique atoms per unit cell) with unit cell sizea0 3.6147 Å. Note that this value of a0 may be calculated from the measured density ρ 8.939 g·cm 3 ,Avogadro’s number 6.0221 1023 atoms per mole, themolecular weight 63.55 g/mole, and the number of atomsper unit cell. Check that this is so. Also calculate interplanar spacing values for planes (200), (220), and (111),which you will be using in the experiment. You shouldidentify in the above figure of cubic unit cells just whichatoms are unique to the unit cell. There are four for facecentered cubic. (How many are there for the other cells?)Incidentally, some common elements like Fe, Cr, Na, andMo crystallize as body centered cubic (BCC), while Cu,Al, Au, and Pb crystallize as face centered cubic (FCC).No element is known to exist in simple cubic form.Before leaving our crystallographic considerations, weshould investigate whether there are restrictions on theappearance of Bragg diffraction from the many (hkl) setsof planes. To illustrate this for our FCC case, a view ofthe unit cell normal to a face shows atoms and atomplanes as shown in Figure 6. There are sheets of atomsseparated by the fundamental distance d(002) a0 /2,with common atomic density in all sheets. If we wereto attempt to observe (001) diffraction as prescribed byBragg’s law, we would find reflected rays (A) and (C) tobe in phase, as would (B) and (D), but the two groupswould be out of phase with respect to each other, andhence overall destructive interference would occur. Thuszero intensity in (001) diffraction is expected, but finiteintensity in (002) diffraction. Without going into detail,the general rule for an FCC structure is that the Millerindices must be either all even integers or all odd integers in order for constructive interference to occur. Thusthere will be no (100), (110), or (221) diffraction occurring, but there can be (020), (111), (022), or (311) forFCC. Other crystal structures would have different selection rules.

Id: 38.neutrons.tex,v 1.97 2014/10/16 15:00:40 spatrick Exp7(A)(B)(C)do(D)d001d002FIG. 6. Illustration of Bragg reflection from a FCC crystal inwhich destructive interference between reflections from adjacent (001) planes occurs.Miller indices can be taken negative as well as positive,and a negative index is written as a bar over the index.Thus (111̄) would designate an allowed set of planes inthe FCC structure Bragg diffraction.FIG. 7. Experimental setup for time-of-flight spectroscopy atthe MIT Nuclear Reactor. [11]Chopper WheelIII.III.1.Chopper slit width 0.965 mmspin axis to beam 54.5 mmAPPARATUSTime-of-Flight SpectrometerspinaxisBF detectorIn all of the present experimentation we shall use apulsed, collimated beam of neutrons emerging from thereactor in a setup shown schematically in Figure 7. Thedistribution in energy of the neutrons in the beam reflects the equilibrium spectrum of the moderated neutrons in the reactor. In accordance with the principlesof statistical physics, we anticipate that this spectrumis the Maxwell-Boltzmann spectrum characterized by atemperature that is the same as the physical temperatureof the moderating agent in the reactor (normal water inthe case of our reactor; some new reactor designs are employing molten salt instead), providing complete moderation of the neutrons has occurred. Thus we can thinkof the neutrons in the reactor as constituting a neutrongas in thermal equilibrium with the moderator, with acertain density and temperature. We will examine thevelocity spectrum of the neutrons by letting some escapeas a collimated beam through a small opening in the reactor shield.We will measure the velocity spectrum by timing theflight of individual neutrons over a laboratory distance ofabout 1.25 meters. We do this by “chopping” the beamas it emerges from the reactor to produce periodic shortbursts of neutron intensity. After traveling the flight distance ,the neutrons are detected with a small neutroncounting tube, and the occurrence times of the individual counting pulses relative to the starting time of theburst are recorded with a multichannel scaler (MCS).III.2.The Neutron ChopperThe chopper is a slotted disk of neutron-absorbing cadmium which rotates about an axis above and parallel toneutron beamfrom reactorfastneutronslowneutronfixed slit1.00 mm wide5.00 mm highLflight distanceFIG. 8. Schematic diagram of the time of flight spectrometershowing the beam chopper and the BF3 detector.the neutron beam line, as illustrated in Figure 8. Cadmium is very absorptive to neutrons of energy less thanabout 0.40 eV (speed of 8760 m/sec), and serves as agood shutter for thermal neutrons. The cadmium diskof thickness 1 mm is sandwiched between two aluminumdisks for mechanical stability. Around the periphery ofthe disk assembly, eight radial slots have been cut. Thewidth of each slot is 0.95 mm. Immediately upstreamof the chopper disk is a fixed slit opening made of neutron absorbing material (boron containing plastic) withwidth 1.00 mm and height 5 mm. This serves

Oct 16, 2014 · Neutron Physics MIT Department of Physics (Dated: October 16, 2014) The technique of time-of-ight spectroscopy with a mechanical beam chopper is used to study the properties of thermal neutrons in a beam emerging from the MIT Research Reactor (MITR-II) at the MIT Nuclear Reactor Laboratory. First, the distribution in velocity of the neutrons is .

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