US2992175A - Neutronic reactor shielding - Google Patents

Neutronic reactor shielding Download PDF

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US2992175A
US2992175A US552559A US55255944A US2992175A US 2992175 A US2992175 A US 2992175A US 552559 A US552559 A US 552559A US 55255944 A US55255944 A US 55255944A US 2992175 A US2992175 A US 2992175A
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shielding
aggregate
neutrons
water
cement
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Lyle B Borst
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    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21CNUCLEAR REACTORS
    • G21C11/00Shielding structurally associated with the reactor
    • G21C11/02Biological shielding ; Neutron or gamma shielding
    • G21C11/028Biological shielding ; Neutron or gamma shielding characterised by the form or by the material
    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21FPROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F1/00Shielding characterised by the composition of the materials
    • G21F1/02Selection of uniform shielding materials
    • G21F1/04Concretes; Other hydraulic hardening materials
    • G21F1/042Concretes combined with other materials dispersed in the carrier
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/30Nuclear fission reactors

Definitions

  • shielding has involved protection against the radiations zfrom radium or similar substances or against X-rays, namely the most common sources of radiation which heretofore have been employed industrially.
  • the use of lead shielding material, certain rubber materials and certain concretes or plasters have been found to constitute satisfactory shielding against X-rays and the like.
  • This invention has for one object to provide an improved shielding medium tfor use against neutrons.
  • Still another object is to provide a shielding medium that is efiective against neutrons of high energies.
  • Still another object is to provide a solid type of shielding medium that is easy to pour or cast into various configurations.
  • a still further object is to provide a shielding medium that is structurally strong and otherwise lends itself to large scale construction and use.
  • Still another object is to provide a shielding material that is susceptible of variation in composition dependent upon the nature and intensity of the radiations against which shielding is desired.
  • Still another object is to provide a shielding material that is particularly useful in shielding chain reactions involving nuclear fission.
  • the construction to be described will be generally referred to as a pile.
  • the pile constitutes an environment in which to expose natural uranium or comparable material under conditions whereby nuclear fission is obtained along with the generation of fission products and various radiations such as neutrons, gamma rays and the like.
  • Various materials i.e. elements having a light nucleus
  • high purity graphite blocks constitute a convenient construction material.
  • Suitable openrectangular or cubical pile is the particular embodiment described herein.
  • the particular dimensions and spacing of the uranium material therein would be governed by the overall size and the amount of material to undergo pile treatment. A construction of the order of 7 to 20 feet or more on each dimension would be satisfactory.
  • suitable openings and channels may be provided for placing in and removing from the pile, the material to undergo the chain reaction. Also openings or conduits may be provided in or through the pile for access thereto for other purposes.
  • control means for operating the pile.
  • regulating and safety means may be comprised of cadmium, boron, mercury, gadolinium or alloys thereof.
  • boron alloy steel is satisfactory.
  • Such materials absorb neutrons. By varying the amount of such material concentrated in the zoneof high neutron activity, the above referred to chain reaction may be controlled.
  • the entire graphite section may be enclosed in my improved shielding composition confining the radiations therewithin as will be described in detail hereinafter.
  • FIG. 1 is a diagrammatic sectional view of a pile construction illustrating one type of unit in connection with which my shielding may be employed.
  • Fig. 2 is a detailed view taken through a section of one species of shielding in accordance with the present invention for showing on a larger scale a composite arrangement of shielding such as has been employed utilizing my invention.
  • FIG. 3 is a sectional view illustrating a section of ordinary concrete for comparative purposes herein.
  • 1 represents the overall construction of an illustrative graphite pile.
  • the passageways 2 are channels for the uranium material as above discussed.
  • the shielding is broadly indicated at 6, and this incloses the graphite 3, but suitable provisions may be made to include openings 17 in the shielding for access to the channels so that the channels may be charged with the metal to undergo fission in the chain reaction.
  • other openings and passageways may be provided as at 4 for the introduction of control means broadly indicated at 5.
  • the particular type of control means is not a limitation on the present invention. The means may be inserted from various points and would be in accordance with good engineering practice. given to desirability of locating control driving mechanism and related parts so as to least interfere with pile operation.
  • control means would preferably be located so that its effectiveness will operate in a zone of high neutron intensity, as for example, in or near the center of the pile graphite or other media in which the chain reaction is being controlled.
  • the shielding 6 as shown may preferably inclose the graphite pile on all sides, but may be spaced therefrom as indicated at 7 to provide passageway through the pile for That is, consideration would be the circulation of the cooling medium such as air.
  • the shielding indicated at 6 represents the broader aspect of my invention. That is, it is similar to ordinary concrete excepting that it contains special aggregate as will be described.
  • Suitable damper means indicated at 8 may be placed at one or more points for controlling and directing the air flow. Other details of construction may be included such as air conduit 9.
  • Metal undergoing fission is indicated at 10.
  • the inner portion of the shielding as indicated at 11 includes the shielding composition of the present invention the component parts of which will be described in detail hereinafter. Surfaces of this inner portion may be coated with a waterproofing .material such as bituminous composition as indicated at 12 and 13 but this is not mandatory. These surfaces may be further .overcoated by standard .cement compositions or slabs indicated at 14 and 15.
  • the particular internal structure, such as the graphite section 3, the cooling means 9 and related parts form no part of the present invention and are not a limitation excepting insofar as the special composition and structure of the present shielding may cooperate therewith.
  • the shielding material may be regarded as somewhat similar to standard concrete in that it is made up of aggregate, cement, and water.
  • this novel shielding material there are certain ingredients incorporated in proportions and under conditions not comparable to ordinary concrete. That is, in shielding material of the present invention, there is incorporated content of barium sulfate (barytes) aggregate.
  • barium sulfate barytes
  • a content of the porous type of aggregate exemplified by that disclosed in Patent No. 1,707,395 of Hayde may be incorporated.
  • a substantially larger amount of water than normally employed may be used.
  • the patent of Hayde discloses in detail a particular type of porous aggregate which I may use as a matter of choice as one of the ingredients of the shielding material.
  • the aggregate is manufactured from a raw material of an argillaceous or clayey character which upon being burned will harden and form a clinker or mass which is subsequently crushed before mixing with the .cementitious ma: terial.
  • the basic raw material is first broken up into suitable sizes which may, for example, be such as to pass a screen of about 4-inch mesh.
  • the material thus prepared is then burned in a suitable kiln at a temperature in excess of 1500 C. so as to first expand the material, destroy the organic matter therein, and produce a hard mass or clinker of cellular formation.
  • the temperature and burning period is regulated so as to give a hard cellular for-mation without burning the material to such an extent as to vitrify it.
  • the individual materials used in making up my shield- 1 ing compositions should be of a good grade. That is,
  • Portland cement may be used, but preferably it should be carefully handled and stored under conditions so that there is no detrimental effect thereupon by moisture or weather conditions. Also, preferably a reasonably new cement, namely one which has not been in storage sufficiently long to have any opportunity to deteriorate .is employed.
  • the aggregates should be substantially free of, orcontain a minimum of soft, friable, thick, flaky, elongatedor laminated particles, ligniteor other deleterious sub-, stances. Also, the aggregate material shouldnot contain strong alkali or organic materials. The size and amount of the aggregate and other related information will be described in further detail below.
  • C3-0'A1203'FE203 410 Calcium sulfate, CaSO 2. to 3.5 Free calcium oxide, CaO 0.1 to 1.0 Magnesium oxide, MgO 1.6 to 3.5 Ignition loss 0.6 to 1.9
  • the fineness modulus preferably is maintained between 2.70 and 2.90.
  • the special aggregate comprised barytes (barium sulfate) of two sizes, the sieve analysis of which is approximately as follows:
  • Example I the general aspects of compositions in accordance with the present invention are illustrated. In the other examples certain species of compositions are illustrated.
  • Example I The components comprising the mix were present in the following percentages ranges by weight on a dry basis.
  • Example 11 l Lbs. Low heat cement-about 7 bags per cu. yd. 658 Special aggregate A plus B 1 2015 Porous type aggregate 943 Mixing water about 55 gals 459 Water absorbed by porous type aggregate about 7% or 66 Total Water 525 Slump approximately 3%" A.S.T.M. Standard Method Strength at 28 days 2000 lbs. to 2500 lbs. per sq. in.
  • a still further example is as follows:
  • Example III Basic weights are per cu. yd. of concrete. Surface moisture content of special aggregate was 11.5%. The sur-. face moisture on the porous type aggregate was estimated as about 5%. The water absorbed by the porous type aggregate was estimated as about 26%.
  • compositions may be used as cast.
  • the surfaces may be sealed with membrane waterproofing or bituminous coatings as indicated in FIG. 2 at 12 and
  • the membrane waterproofing and the bituminous coating are commercially obtainable materials which are waterproof and serve to deter moisture evaporation from the cement. Such material is applied to form a complete and impervious moi-sture'retaining envelope.
  • a coat of conventional primer may be applied before these finishes are applied on the shielding.
  • the concrete In the compositions containing porous aggregate preferably the concrete would be kept Wet but not to the extent of dripping.
  • the porous type aggregate material may absorb 25 percent or more of water and hence the material preferably is kept near this saturation. Spraying should be done carefully and uniformly, preferably within approximately 4.8 hours previous to use.
  • compositions in accordance with this invention may require slightly more time for mixing than standard ma terials and hence the mixing time may be increased to a minimum of 1 /2 minutes but excessive mixing is to be avoided to prevent pulverizing the aggregates involved.
  • Full speed mixing time usually may be limited to about 2 /2 or 3 minutes.
  • compositions in accordance with this invention are poured or cast in a conventional manner.
  • the porous type aggregate ingredient may be' reduced or omitted and a satisfactory neutron shielding still obtained;
  • the compositions may be fabricated' into any desired configuration as for example the structure shown in FIG. 2 may be poured.
  • the proportions chosen are such that larger amounts of the finer aggregate are present to obtain workability.
  • FIG. 2 there is diagrammatically shown a section of shielding of a measured thickness of a composition in accordance with the present invention. That is, the composition indicated by reference numeral 11 was of a mix in accordance with Example IV. This inner section 11 was coated with bituminous'materials at 1 2 and 13 and layers of ordinary concrete applied at 14 and 15.
  • the overall width or thickness W of the shielding of FIG. 2 was the same as the overall Width or thickness W of an equivalent amount of ordinary cement diagrammatically shown in FIG. 3. In the particular situation being described W was approximately seven feet.
  • an extended source of equal intensity of fast neutrons was applied against one side of the shielding.
  • extended source reference is made to a relatively widely destributed source of neutrons as compared with a point source or beam. This source is indicated by the symbol I and probably was of the order of neutrons per square centimeter per second. However, since the intensity was of the same magnitude in both instances, the specific value thereof is not material for the purposes of this comparison.
  • the shielding material in accordance with the. present invention may be substituted for or used in conjunction with conventional means that have been employed for shielding cyclotrons or other neutron generating units not only with the advantage of easier fabrication and upkeep, but in many instances being considerable more economical to install.
  • My shielding may comprise concrete with only a'content of barium sulfate as above described and such material is effective against fast neutrons.
  • the porous type aggregate component may be omitted or reduced in quantity.
  • a content of porous type aggregate or other water absorbing aggregate in some instances may be employed in addition to my invention relative to using barium sulfate.
  • composition as respect solid components in a mix will comprise cement 15% to 45%, special barytes component 30% to 60%, and other aggregates or conventional components from a small amount to 40%.
  • Sufiicient Water would be added in accordance with the principles illustrated in the above examples to' obtain good mixing and adequately wet porous aggregate if any has been included.
  • compositions may be made in the composition as for example certain iron compounds such as iron oxides, sulfides or the like may be included for supplementing the content of barytes. Other changes will occur to those skilled in the art.
  • improved neutron-shield means comprising a mass of solid hydrogenous concrete composition compounded of cement, water, and aggregate, at least a portion of said aggregate comprising barytes, ingredients other than water being in approximately the following proportions by weight: cement 15 to 45%, barytes aggregate 30 to 60%, and the balance other aggregate, said cement comprising the following ingredients in substantially the indicated ranges of proportions by weight:
  • Tricalcium silicate 3CaO.SiO 21 to 45 Dicalcium silicate, 2CaO.SiO 25 to 50 Tricalcium aluminate, 3CaO.Al O 4 to 8 Tetracalcium alumino-ferrite, 4CaO.A1 O .Fe O t Calcium sulfate, CaSO 2 to 3.5 Free calcium oxide, CaO 0.1 to 1.0 Magnesium oxide, MgO 1.6 to 3.5

Description

July 11, 1961 B. BORST NEUTRONIC REACTOR SHIELDING Filed Sept. 2, 1944 u I ...Q
N3 Fa INVENTOR. Kyle B. Batu-Z N N S K M NRQQ United States Patent Ofice 2,992,175 Patented July ll, 1961 r 2,992,175 NEUTRONIC REACTOR SHIEIJDING Lyle B. Borst, 'Oak Ridge, Tenn., assignor to the United States of America as represented by the United States Atomic Energy Commission Filed Sept. 2, 1944, Ser. No. 552,559 1 Claim. (Cl. 204-1932) This invention relates to improvements in shielding against radioactivity. More particularly, this invention concerns improved shielding against very high activities and particularly activities such as neutrons.
Whilc certain radioactive emanations have been known and used for some time and have served many useful purposes, it has also been appreciated that there is considerable danger associated with the handling and use of such radiations. It has already been proposed in the art to use shielding for protecting workers and equipment. However, compared with the magnitude and type of radiations obtainable at present, the prior art methods of shielding are insufficient.
In the past shielding has involved protection against the radiations zfrom radium or similar substances or against X-rays, namely the most common sources of radiation which heretofore have been employed industrially. The use of lead shielding material, certain rubber materials and certain concretes or plasters have been found to constitute satisfactory shielding against X-rays and the like. I
More recently, however, with the advent of the cyclotron, the subject'of shielding has again presented problems not only because of the greater intensities of radiations, but because of the emission of neutrons against which shielding is required. The publication Applied Nuclear Physics by Pollard and Davidson, published by John W. Wiley & Sons, New York, 1942, discusses protection against radiations including the protection against cyclotron radiations. For example, it is thereindicated that water'or other hydrogen-containing media is the principal shielding material for use against neutrons. While tanks containing water under certain conditions constitute effective neutron shielding, it is apparent that the fabrication of complicated shielding configurations tor containingwater is limited or presents considerable difliculty. Also, there is the attendant danger that tanks may leak thereby rendering the shielding ineffective. In addition, water is not too effective at high neutron energies but functions at neutron energies below 100,000 electron volts, namely low energy and slow neutrons.
Recently there have been other developments in method and means of producing radiations whereby there are obtained neutron emissions and other radiations of a magnitude which far exceeds the intensities previously obtained by means of the largest X-ray equipment, cyclotron or similar devices. When it is considered that the activity involved is comprised largely of neutrons, and that neutrons are several timm more potent than, for
example, gamma or X-r-ays, it is apparent that the provision of suitable shielding" for such high intensity sources presents a problem of considerable magnitude.
I have found, however, a solid 'type of shielding material for use against such radiations which may be em ployed either alone or in conjunction with media such as water or other hydrogen-containing substances.
This invention has for one object to provide an improved shielding medium tfor use against neutrons.
Still another object is to provide a shielding medium that is efiective against neutrons of high energies.
Still another object is to provide a solid type of shielding medium that is easy to pour or cast into various configurations.
A still further object is to provide a shielding medium that is structurally strong and otherwise lends itself to large scale construction and use.
Still another object is to provide a shielding material that is susceptible of variation in composition dependent upon the nature and intensity of the radiations against which shielding is desired.
Still another object is to provide a shielding material that is particularly useful in shielding chain reactions involving nuclear fission.
Other objects will appear hereinafter.
I have found that certain types of cement or concrete compositions containing in addition to or in place of certain of the standard ingredients such as cement, aggregate, sand, water, and the like, but also containing barium sulfate not only forms a shielding medium against gamma rays but provides a shielding medium which efiectively slows down fast neutrons. I have found that the material of the present invention is particularly useful in forming a shielding medium for surrounding a chain reaction involving nuclear fission, as for example, the shielding of a pile or comparable unit.
Inasmuch as the types of reactions giving ofi neutrons of high energy and related information concerning the generation of extremely high intensity radiation is relatively new and known in the art to a limited extent, cer tain preliminary description is set forth primarily for background. That is, the construction of means for accomplishing nuclear reactions involving fission and the operations of such nuclear reactions therein are described below for giving a better understanding of the conditions and environment under which my improved shielding may be utilized. However, the specific details of constructing a pile, neutron reactor, or comparable device for carrying out chain reactions is not a limitation on the present invention, and is not claimed herein excepting insofar as it may cooperate with the particular shielding described.
The construction to be described will be generally referred to as a pile. The pile constitutes an environment in which to expose natural uranium or comparable material under conditions whereby nuclear fission is obtained along with the generation of fission products and various radiations such as neutrons, gamma rays and the like.
Various materials (i.e. elements having a light nucleus) as heavy hydrogen, helium, beryllium, and carbon may be used as the environment for the material undergoing fission. For example, high purity graphite blocks constitute a convenient construction material. Suitable openrectangular or cubical pile is the particular embodiment described herein. The particular dimensions and spacing of the uranium material therein would be governed by the overall size and the amount of material to undergo pile treatment. A construction of the order of 7 to 20 feet or more on each dimension would be satisfactory. As indicated, suitable openings and channels may be provided for placing in and removing from the pile, the material to undergo the chain reaction. Also openings or conduits may be provided in or through the pile for access thereto for other purposes.
There may also be provided adequate control means -for operating the pile. This would include rods, compressible springs orthe like, designated as regulating means or shim rods, positioned within or adapted to be inserted into the pile in a manner so that the effective amount thereof may be varied. These regulating and safety means may be comprised of cadmium, boron, mercury, gadolinium or alloys thereof. For example, boron alloy steel is satisfactory. Such materials absorb neutrons. By varying the amount of such material concentrated in the zoneof high neutron activity, the above referred to chain reaction may be controlled. The entire graphite section may be enclosed in my improved shielding composition confining the radiations therewithin as will be described in detail hereinafter.
When a properly constructed pile has been charged with auranium material, such as natural uranium including a content of uranium U and the control means are adjusted, fission will be brought about by a random slow neutron r bythe spontaneous splitting of an atom of U As is known, natural uranium has a concentration of about one part U to 139 parts of U When fission occurs in the environment described with the emission of neutrons, the neutrons that escape from the apparatus are limited and the speeds of others are reduced, permitting the setting up of a chain reaction. By suitable control, as indicated, the chain reaction proceeds giving 06 intense radiations.
For further understanding of the construction which has been discussed broadly in the preceding paragraphs, reference is made to the attached drawing forming a part of the present application.
FIG. 1 is a diagrammatic sectional view of a pile construction illustrating one type of unit in connection with which my shielding may be employed. Fig. 2 is a detailed view taken through a section of one species of shielding in accordance with the present invention for showing on a larger scale a composite arrangement of shielding such as has been employed utilizing my invention. FIG. 3 is a sectional view illustrating a section of ordinary concrete for comparative purposes herein.
Referring to FIG. 1, 1 represents the overall construction of an illustrative graphite pile. The passageways 2 are channels for the uranium material as above discussed. The shielding is broadly indicated at 6, and this incloses the graphite 3, but suitable provisions may be made to include openings 17 in the shielding for access to the channels so that the channels may be charged with the metal to undergo fission in the chain reaction. Also other openings and passageways may be provided as at 4 for the introduction of control means broadly indicated at 5. The particular type of control means is not a limitation on the present invention. The means may be inserted from various points and would be in accordance with good engineering practice. given to desirability of locating control driving mechanism and related parts so as to least interfere with pile operation.
The control means, however, would preferably be located so that its effectiveness will operate in a zone of high neutron intensity, as for example, in or near the center of the pile graphite or other media in which the chain reaction is being controlled.
The shielding 6 as shown may preferably inclose the graphite pile on all sides, but may be spaced therefrom as indicated at 7 to provide passageway through the pile for That is, consideration would be the circulation of the cooling medium such as air. The shielding indicated at 6 represents the broader aspect of my invention. That is, it is similar to ordinary concrete excepting that it contains special aggregate as will be described. Suitable damper means indicated at 8 may be placed at one or more points for controlling and directing the air flow. Other details of construction may be included such as air conduit 9. Metal undergoing fission is indicated at 10.
Referring now to the shielding construction, one special embodiment is as shown in FIG. 2. The inner portion of the shielding as indicated at 11 includes the shielding composition of the present invention the component parts of which will be described in detail hereinafter. Surfaces of this inner portion may be coated with a waterproofing .material such as bituminous composition as indicated at 12 and 13 but this is not mandatory. These surfaces may be further .overcoated by standard .cement compositions or slabs indicated at 14 and 15.
As indicated, the particular internal structure, such as the graphite section 3, the cooling means 9 and related parts form no part of the present invention and are not a limitation excepting insofar as the special composition and structure of the present shielding may cooperate therewith.
Considering now the composition of the shielding material with which the present invention is particularly concerned, its method of preparation and related details are described below.
In general, the shielding material may be regarded as somewhat similar to standard concrete in that it is made up of aggregate, cement, and water. However, in this novel shielding material there are certain ingredients incorporated in proportions and under conditions not comparable to ordinary concrete. That is, in shielding material of the present invention, there is incorporated content of barium sulfate (barytes) aggregate. In certain special embodiments a content of the porous type of aggregate exemplified by that disclosed in Patent No. 1,707,395 of Hayde may be incorporated. Also in certain species a substantially larger amount of water than normally employed may be used.
The patent of Hayde discloses in detail a particular type of porous aggregate which I may use as a matter of choice as one of the ingredients of the shielding material. The aggregate is manufactured from a raw material of an argillaceous or clayey character which upon being burned will harden and form a clinker or mass which is subsequently crushed before mixing with the .cementitious ma: terial. In manufacturing the aggregate the basic raw material is first broken up into suitable sizes which may, for example, be such as to pass a screen of about 4-inch mesh. The material thus prepared is then burned in a suitable kiln at a temperature in excess of 1500 C. so as to first expand the material, destroy the organic matter therein, and produce a hard mass or clinker of cellular formation. The temperature and burning period is regulated so as to give a hard cellular for-mation without burning the material to such an extent as to vitrify it.
The individual materials used in making up my shield- 1 ing compositions should be of a good grade. That is,
Portland cement may be used, but preferably it should be carefully handled and stored under conditions so that there is no detrimental effect thereupon by moisture or weather conditions. Also, preferably a reasonably new cement, namely one which has not been in storage sufficiently long to have any opportunity to deteriorate .is employed.
The aggregates should be substantially free of, orcontain a minimum of soft, friable, thick, flaky, elongatedor laminated particles, ligniteor other deleterious sub-, stances. Also, the aggregate material shouldnot contain strong alkali or organic materials. The size and amount of the aggregate and other related information will be described in further detail below.
Percent Tricalcium silicate, 3 CaO=-Si 21 to 45 Dicalcium silicate, 2. CaO-SiO 25 to 50 Tnicalcium aluminate, 3 CaO-Al O 4 to 8 Tetracalcium alurnino-fernite, 4
C3-0'A1203'FE203 410 Calcium sulfate, CaSO 2. to 3.5 Free calcium oxide, CaO 0.1 to 1.0 Magnesium oxide, MgO 1.6 to 3.5 Ignition loss 0.6 to 1.9
The sieve analysis of the particular porous type of aggregate described above, used in some of the as described herein conformed approximately to the following:
Percent Actual Sieve No. Passing Test,
Limits Percent Passing The fineness modulus (F.M.) preferably is maintained between 2.70 and 2.90.
The special aggregate comprised barytes (barium sulfate) of two sizes, the sieve analysis of which is approximately as follows:
' Aggregate Aggregate BieveNo. or. Size of Mesh A", Percent B," Percent Passing Passing F.M.= 3.33 to 2.58
A further understanding of my invention may be had by a consideration of the following examples. In Example I the general aspects of compositions in accordance with the present invention are illustrated. In the other examples certain species of compositions are illustrated.
Example I The components comprising the mix were present in the following percentages ranges by weight on a dry basis.
, Percent Low heat cement 15 to 4 5 Special aggregate A and/or B 30 to 60 Sand or other conventional ingredients 0 to 40 .Sufficient water, in accordance with the practice in the art, to obtain good mixing was incorporated with the above ingredients.
' Examples of illustrating species of compositions under the invention are described below.
Example 11 l Lbs. Low heat cement-about 7 bags per cu. yd. 658 Special aggregate A plus B 1 2015 Porous type aggregate 943 Mixing water about 55 gals 459 Water absorbed by porous type aggregate about 7% or 66 Total Water 525 Slump approximately 3%" A.S.T.M. Standard Method Strength at 28 days 2000 lbs. to 2500 lbs. per sq. in.
Special aggregate 50% "A" and 50% B with permissible variation i5%.
A still further example is as follows:
Example III Basic weights are per cu. yd. of concrete. Surface moisture content of special aggregate was 11.5%. The sur-. face moisture on the porous type aggregate was estimated as about 5%. The water absorbed by the porous type aggregate was estimated as about 26%.
Basic dry weight Cement7.5 bags (per cubic yard) lbs 705 Special aggregate (barytes) ..lbs 1991 Porous type aggregate lbs.. '892 Mixing water added-48 gal. Surface water in special aggregate 1.5%'=30 lbs.
Surface water in Haydite 5%=45 lbs.
75 lbs.=9 gal.)
Lbs.
Total water-57 gal. 475
Water absorbed by Haydite-26% 23 1 Strength about 2 400 lbs. per sq. in. at 28 days Slump, approx. 5 /2" A.S.T.M. Standard Method- Example IV Basic dry weight Porous type aggregate sand (moisture 33%) lbs 1779 Barium sulfate coarse aggregate "lbs-.. 3017 Low heat cement lbs 1058 Water gal 61 Example V Basic dry weight Porous type aggregate sand lbs 1177 Barium sulfate coarse aggregate -Elbs-.. 2021 Low heat cement lbs 705 Water gal 42 Slump (A.S.T.M. Standard Method) in 6 The chemical composition of the low heat Portland cement used in Examples IV and V was:
Symbol Percentage Chemical Compound 44. 24 Tricalcium Silicate.
Dicalcium Silicate. Tricalcium Aluminate.
Tetracalclum Alumlno Ferrite.
The correct design for any shielding using the above ingredients would preferably result from trial batches run to determine any peculiarities of given ingredients.
The above compositions may be used as cast. However, with respect to the composition containing large amounts of water, in addition to the barium sulfate content in accordance with my invention, if desired, the surfaces may be sealed with membrane waterproofing or bituminous coatings as indicated in FIG. 2 at 12 and The membrane waterproofing and the bituminous coating are commercially obtainable materials which are waterproof and serve to deter moisture evaporation from the cement. Such material is applied to form a complete and impervious moi-sture'retaining envelope. A coat of conventional primer may be applied before these finishes are applied on the shielding.
Care should be observed in rodding the concrete compositions in place to secure density and accurate placement and at the same time preserve the accuracy of the work without disturbing inserts, pipes, sleeves and the like.
In the compositions containing porous aggregate preferably the concrete would be kept Wet but not to the extent of dripping. The porous type aggregate material may absorb 25 percent or more of water and hence the material preferably is kept near this saturation. Spraying should be done carefully and uniformly, preferably within approximately 4.8 hours previous to use.
Compositions in accordance with this invention may require slightly more time for mixing than standard ma terials and hence the mixing time may be increased to a minimum of 1 /2 minutes but excessive mixing is to be avoided to prevent pulverizing the aggregates involved. Full speed mixing time usually may be limited to about 2 /2 or 3 minutes.
The compositions in accordance with this invention are poured or cast in a conventional manner.
If mechanical vibration is utilized this should be carefullycarried out. Since the ingredients used in the compositionof thisinventionmay differ materially in weight,
there may be a tendency toward segregation and this is avoided; Effort is made to keep the temperature of the composition as low as possible by proper wetting and curing methods, and as stated previously, with respect to certain of the compositions care is taken to retain all moisture within the body of the composition until a membrane or moisture sealing envelope is applied.
In the above mixes the porous type aggregate ingredient may be' reduced or omitted and a satisfactory neutron shielding still obtained; The compositions may be fabricated' into any desired configuration as for example the structure shown in FIG. 2 may be poured. When intricate shapes are involved or inserts as plugs 17 are to be included, the proportions chosen, are such that larger amounts of the finer aggregate are present to obtain workability.
The property of the shielding described herein for slowing downfast'neutrons' is indicated by the following comparison, reference beingmade to FIGS. 2 and 3.
In FIG. 2 there is diagrammatically shown a section of shielding of a measured thickness of a composition in accordance with the present invention. That is, the composition indicated by reference numeral 11 was of a mix in accordance with Example IV. This inner section 11 was coated with bituminous'materials at 1 2 and 13 and layers of ordinary concrete applied at 14 and 15.
The overall width or thickness W of the shielding of FIG. 2 was the same as the overall Width or thickness W of an equivalent amount of ordinary cement diagrammatically shown in FIG. 3. In the particular situation being described W was approximately seven feet.
For the purpose of comparing the shielding value, an extended source of equal intensity of fast neutrons was applied against one side of the shielding. By extended source reference is made to a relatively widely destributed source of neutrons as compared with a point source or beam. This source is indicated by the symbol I and probably was of the order of neutrons per square centimeter per second. However, since the intensity was of the same magnitude in both instances, the specific value thereof is not material for the purposes of this comparison.
Evidence of neutrons on the opposite side of the shielding of FIG. 2 away from the source was tested for and nonewere detected. Ontheother hand, with respect to The ratio of I to 1 of FIG. 2 was of the-order of The ratio of I, to I of FIG. 3 was of the order of In this comparison it will be kept in mind that the I represents a source of neutrons of all energiesto theupper limit of the fission energy spectrum. It will be observed that the shielding of FIG. 2 in accordance with the present invention reduced the intensity of the fast neutrons (the most penetrating component) many hundreds of thousands of times that of the same thickness of the ordinary cement section represented in FIG. 3.
It has been found that for fast neutrons the barium sulfate containing concrete compositions in accordance with the present invention, particularly where the neutron intensity is in excess of two million electron volts' is especially effcctive in slowing down such neutrons.
At the order of one hundred thousand electron volts or less water is an effective medium. Therefore, in some of the species of compositions of the present invention where both barium sulfate and a water content are present, neutron emissions of high intensity may be readily shielded against.
From the foregoing it will be noted that while certain of the species of shielding compositions may contain;
substantial amounts of water and while it is'known thatwater shields against neutrons, the content of water in the compositions of the present invention is insufiicient to account for the ability to slow down neutrons. ,Consequently, it is apparent that the ingredients, particularly the barium sulfate content, as above described cooperate in. some manner to provide a material particularly effective in slowing down fast neutrons as well as shielding against gamma radiations. Although it has been known that barium sulfate functions as a shielding medium against X-rays, it is believed that it has not heretofore been known in the art that this material would also function to slow down fast neutrons-whileat the same time acting as shielding against gamma radiations.
The shielding material in accordance with the. present invention may be substituted for or used in conjunction with conventional means that have been employed for shielding cyclotrons or other neutron generating units not only with the advantage of easier fabrication and upkeep, but in many instances being considerable more economical to install.
My shielding may comprise concrete with only a'content of barium sulfate as above described and such material is effective against fast neutrons. In the above compositions the porous type aggregate component may be omitted or reduced in quantity. However, as indicated, a content of porous type aggregate or other water absorbing aggregate in some instances, may be employed in addition to my invention relative to using barium sulfate.
In general the composition as respect solid components in a mix will comprise cement 15% to 45%, special barytes component 30% to 60%, and other aggregates or conventional components from a small amount to 40%. Sufiicient Water would be added in accordance with the principles illustrated in the above examples to' obtain good mixing and adequately wet porous aggregate if any has been included.
Certain changes may be made in the composition as for example certain iron compounds such as iron oxides, sulfides or the like may be included for supplementing the content of barytes. Other changes will occur to those skilled in the art.
It is to be understood that all matters contained in the above description and examples are illustrative only and do not limit the scope of this invention, as it is intended to claim the invention as broadly as possible in view of the prior art.
I claim:
In a neutronic nuclear fission reactor including neutron-shield for restraining the egress of neutron radiation therefrom, improved neutron-shield means comprising a mass of solid hydrogenous concrete composition compounded of cement, water, and aggregate, at least a portion of said aggregate comprising barytes, ingredients other than water being in approximately the following proportions by weight: cement 15 to 45%, barytes aggregate 30 to 60%, and the balance other aggregate, said cement comprising the following ingredients in substantially the indicated ranges of proportions by weight:
Percent Tricalcium silicate, 3CaO.SiO 21 to 45 Dicalcium silicate, 2CaO.SiO 25 to 50 Tricalcium aluminate, 3CaO.Al O 4 to 8 Tetracalcium alumino-ferrite, 4CaO.A1 O .Fe O t Calcium sulfate, CaSO 2 to 3.5 Free calcium oxide, CaO 0.1 to 1.0 Magnesium oxide, MgO 1.6 to 3.5
10 References Cited in the file of this patent UNITED STATES PATENTS 1,576,730 Harth Mar. 16, 1926 1,707,395 Hayde Apr. 2, 1929 1,744,869 Cross Jan. 28, 1930 1,943,584 Cross Jan. 16, 1934 2,206,634 Fermi July 2, 1940 2,231,577 Hare Feb. 11, 1941 2,398,347 Anderson Apr. 16, 1946 FOREIGN PATENTS 114,150 Australia May 2, 1940 OTHER REFERENCES American Journal of Roentgenology and Radium Therapy, April 1925 (pages 383 and 384).
Atomics, volume 6, No. 6, pages 4l5, November- December, 1950, published bi-monthly by Technical Publishing Company, Chicago 3, Illinois.
Hackhs Chemical Dictionary, pages 97, 99, 100, 1946, printing of third edition copyrighted 1944, Blakiston.
Smyth: A General Account of the Development of Methods of Using Atomic Energy for Military Purposes under the Auspices of the United States Government, published August 1945, for Sale by Superintendent of Documents, Washington, D.C., pages 22, 25, 27.
The Science and Engineering of Nuclear Power by Clark Goodman, published by Addison-Wesley Press, Inc. (1947). Pages 275.
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US3141055A (en) * 1958-12-01 1964-07-14 Schmitt Wilhelm Open hearth smelter system
US3169932A (en) * 1962-03-21 1965-02-16 Pakistan Council Of Scient And Method of producing artificial marble from barium sulfate and aqueous alkali silicate
US3239422A (en) * 1960-03-11 1966-03-08 Atomic Energy Authority Uk Gas cooled nuclear reactor with improved shield and control rod arrangement
US3780309A (en) * 1970-07-28 1973-12-18 Robatel Slpi Insulated container for radioactive and like substances
US4257912A (en) * 1978-06-12 1981-03-24 Westinghouse Electric Corp. Concrete encapsulation for spent nuclear fuel storage
US4366114A (en) * 1979-07-20 1982-12-28 Kraftwerk Union Ag Dry storage for spent fuel assemblies
US5673528A (en) * 1992-04-03 1997-10-07 Siemens Aktiengesellschaft Safety wall for a building
US6565647B1 (en) 2002-06-13 2003-05-20 Shieldcrete Ltd. Cementitious shotcrete composition
US20070102672A1 (en) * 2004-12-06 2007-05-10 Hamilton Judd D Ceramic radiation shielding material and method of preparation
US20090159852A1 (en) * 2007-12-21 2009-06-25 Construcciones Tecnicas De Radio Terapia, S.L. Heavy mass for the execution of radioprotection barriers in an X-ray environment
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US1707395A (en) * 1920-02-10 1929-04-02 American Aggregate Company Method of burning argillaceous material and product resulting therefrom
US1744869A (en) * 1925-04-20 1930-01-28 Silica Products Co Waterproof concrete and process of making same
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US2206634A (en) * 1934-10-26 1940-07-02 G M Giannini & Co Inc Process for the production of radioactive substances
US2231577A (en) * 1940-05-29 1941-02-11 Texaco Development Corp Locating cement
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US1707395A (en) * 1920-02-10 1929-04-02 American Aggregate Company Method of burning argillaceous material and product resulting therefrom
US1576730A (en) * 1924-04-04 1926-03-16 Nat Pigments & Chemical Compan Plaster or concrete opaque to x-rays
US1744869A (en) * 1925-04-20 1930-01-28 Silica Products Co Waterproof concrete and process of making same
US1943584A (en) * 1929-03-28 1934-01-16 Silica Products Co Inorganic gel composition
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Publication number Priority date Publication date Assignee Title
US3141055A (en) * 1958-12-01 1964-07-14 Schmitt Wilhelm Open hearth smelter system
US3239422A (en) * 1960-03-11 1966-03-08 Atomic Energy Authority Uk Gas cooled nuclear reactor with improved shield and control rod arrangement
US3169932A (en) * 1962-03-21 1965-02-16 Pakistan Council Of Scient And Method of producing artificial marble from barium sulfate and aqueous alkali silicate
US3780309A (en) * 1970-07-28 1973-12-18 Robatel Slpi Insulated container for radioactive and like substances
US4257912A (en) * 1978-06-12 1981-03-24 Westinghouse Electric Corp. Concrete encapsulation for spent nuclear fuel storage
US4366114A (en) * 1979-07-20 1982-12-28 Kraftwerk Union Ag Dry storage for spent fuel assemblies
US5673528A (en) * 1992-04-03 1997-10-07 Siemens Aktiengesellschaft Safety wall for a building
US6565647B1 (en) 2002-06-13 2003-05-20 Shieldcrete Ltd. Cementitious shotcrete composition
US20070102672A1 (en) * 2004-12-06 2007-05-10 Hamilton Judd D Ceramic radiation shielding material and method of preparation
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US8440108B2 (en) 2005-12-06 2013-05-14 Co-Operations, Inc. Chemically bonded ceramic radiation shielding material and method of preparation
USRE46797E1 (en) 2005-12-06 2018-04-17 Co-Operations, Inc. Chemically bonded ceramic radiation shielding material and method of preparation
USRE48014E1 (en) 2005-12-06 2020-05-26 Co-Operations, Inc. Chemically bonded ceramic radiation shielding material and method of preparation
US20090159852A1 (en) * 2007-12-21 2009-06-25 Construcciones Tecnicas De Radio Terapia, S.L. Heavy mass for the execution of radioprotection barriers in an X-ray environment
US20200027593A1 (en) * 2018-07-04 2020-01-23 Rolls-Royce Plc Nuclear power plant

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