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Publication numberUS3033797 A
Publication typeGrant
Publication dateMay 8, 1962
Filing dateApr 19, 1957
Priority dateApr 19, 1957
Publication numberUS 3033797 A, US 3033797A, US-A-3033797, US3033797 A, US3033797A
InventorsDe Leo Felix R, Edward Shapiro
Original AssigneeLuminous Products Corp
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Self-luminous paints
US 3033797 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 3,033,797 Patented May 8, 1962 3,033,797. SELF-LUMIN US PAINTS Felix R. De Leo, Needham, and Edward Shapiro, Newton, Mass, assignors, by mesne assignments, to Luminous Products Corp., Boston, Mass a corporation of Massachusetts No Drawing. Filed Apr. 19, 1957, Ser. No. 653,733 3 Claims. (Cl. 252-3011) This invention relates to a self-luminous paint and more particularly to a self-luminous paint comprising the radioactive isotope tritium.

Heretotore self-luminous paints have been made using as the exciting agent a compound of radium. Generally the radium compound is in intimate admixture with the phosphor crystals and is not an integral part of the paint vehicle. Unfortunately radium is a particularly dangerous form of radioactive material since when ingested by the body, it has a tendency to lodge in the bony structurewith its radiations causing serious damage to surrounding tissue. In addition, radium and its radioactive descendants emit penetrating gamma radiation which results in continual radiation doses to those who are eX- posed to it as, for example, workers Who apply radium self-luminous paints to watch, clock and instrument dials. A further disadvantage of radium paints lies in the fact that the alpha particles emitted by radium are capable of destroying the phosphorescent quality of the phosphor crystals in the paint, so that a radium paint loses about one-half of its original brightness each year following compounding of the paint. Thus there is a limited useful period for any radium paint. A luminous watch, clock or instrument dial which is several years old will be found to havelost most of its original luminosity.

Because of these and other disadvantages, efforts have been made to produce self-luminous paints superior to radium paints.

Accordingly it is the purpose of this invention to provide a self-luminous paint which avoids the aforementioned difiiculties common to radium paints.

In particular it is the object of this invention to provide a selfrluminous paint in which the radioactive isotope tritium is used to furnishthe energy forexcitation of the phosphor to produce luminescence, thereby eliminating radium with all of its concomitant disadvantages.

Another specific object of this invention is to provide a self-luminous paint which can be prepared and used without hazard to personnel and which can be applied by brushing, dipping or silk screening, as desired.

Another object of the present invention is to provide a self-luminous paint comprising a predetermined amount of phosphor particles of predetermined size and tritiated hydrogenous paint vehicle which is substantially nonvolatile. 7

Other objects and many of the attendant advantages of the present invention willrbecome' more apparent as reference is had to the following detailed description.

By the present invention it is proposed to provide a self-luminous paint comprising an intimate mixture of a pigment which is a phosphorescent'material, a tritiated vehicle, the vehicle comprising either a substantially nonvolatile hydrogenous plastic binder alone or a plastic binder combined with an hydrogenous substantially nonvolatile paint modifier such as a plasticizer, and a solvent for the vehicle.

' In developing this invention it has been determined that the choice of phosphor is determined by two factors: (1) the efficiencyof conversion of beta-ray energy to visible light, and (2) the size of the phosphor particles. The first factor is believed to. be obvious. The second factor can be demonstrated as follows:

Assume a paint mixture which upon drying contains 100 grams of phosphor dispersed uniformly throughout 100 grams of tritiated plastic, the phosphor and plastic having the following physical characteristics: a

( 1) Density of plastic -L- 1.25 grams/cmfi. (2) Density of phosphor 4.00 grams/cm. (3) Volume of plastic 100/ 1.25:80 cmfi. (4) Volume of phosphor l00/4.0=2S cm. (5) Volume of paint 105 cm.

Number of phosphor particles in the length of a cube is (4.8 10 =3.6X10 The number of phosphor particles per centimeter length 3.6 X l0 /4.7=7.7 X 10 j The average distance between the centers of individual particles is l/7.7 10 =l.3 X10 cm.

' Since the average diameter of the phosphor particles is 1.0x 10- cm., the distance between phosphor particle surfaces is 1.3 10-' minus 1.0x l0- or This thickness of plastic is less than one twenty-fifth the range of tritium beta rays in the plastic, so that an appreciable fraction of beta radiation Will strike phosphor particles, exciting them to luminescence.

' Case B:

Average diameter of phosphor particles is 10 microns (.001 cm.).

By calculations analogous to the foregoing, it will be found that the average distance between phosphor particles surfaces is 03x10" cm. This corresponds to a plastic thickness nearly one-half the range of tritium beta rays in the plastic. In such 'a case it has been found that approximately 90% of the beta energy will be expended in the plastic, resulting in'poor luminous eificiency.

From extensive research'it has been discovered that for a given amount of radioactivity best results are obtained when the phosphor particles have a maximum average size in the range of 1 to 2 microns. At the same concentration of radioactivity, increasing thesize of the particles to 3 microns gives satisfactory results, although the efficiency is somewhat lower than with particles of 2 microns. Above 3 microns the efiiciency drops rapidly, but the loss in efiiciency due to the increase in phosphor particle size can be compensated for by increasing the concentration of radioactivity As pointed out more fully hereinafter,

. increasing the-concentration of tritium does not increase the rate of loss of brightness. Accordingly, particle sizes up to approximately 10 micronsaverage diameter may be used if the concentration of tritium is also increased. However, in view of the relatively high cost of tritium, it is more economical to use particles having a maximum diameter of 3 microns or less because of the markedly greater efiiciency that results. Of course particles smaller than 1 micron will give even better results. Unfortunately smaller particles having good efficiency of conversion of beta-ray energy to visible light are not available commercially.

Fortunately there are various phosphors available in the desired sizes. Zinc orthosilicate: manganese activated phosphor is available in 1 and 2 micron average diameter, and has-been found to be eminently suitable for use in formulating a tritium self-luminous paint. A silicate phosphor is preferred to a sulfide phosphor inasmuch as it is more resistant to the deleterious action of moisture and high energy radiations. This choice, however, is not to rule out the use of other phosphors such as 1) zinc sulphide: copper; (2) zinc sulphide: silver; (3) zinc cadmium sulfide: copper; or other types such as zinc orthogermanate when these are available as eflicient phosphors with small 1 to 3 (and preferably 1 to 2) micron diameters.

The choice of phosphor will determine the color of the paint. A blue paint can be made by using calcium magnesium silicate: titanium activated. A green paint results from using zinc orthosilicate: manganese activated. A yellow paint can be prepared using zinc cadmium sulfide: silver activated. A red paint can be made with zinc phosphate: manganese activated. Similarly, an orange paint can be obtained using zinc cadmium sulfide: silver activated.

Speaking generally a self-luminous paint comprises a phosphor, a vehicle, a solvent and a source of radioactive energy for exciting the phosphor to luminescence. As used herein the term vehicle excludes the volatile components of an ordinary paint and includes not only the plastic binder but the plastic binder in combination with any other modifying agent as, for example, a plasticizer, which is compatible with the binder and is non-volatile. In the present invention the tritium is chemically combined in the vehicle, either by tritiation of the plastic hinder or by tritiation of the plasticizer or other nonvolatile hydrogenous modifying agent included in the vehicle as defined herein.

Preparation of Tritiated Plastic Binder The vehicle of the paint may comprise a tritiated plastic. Thus, for example, tritiated polyvinyl acetate can be used as the plastic binder component of the vehicle of a self-luminous paint. This plastic is prepared first as a monomer, vinyl acetate, by the following reactions, and the monomer subsequently polymerized to polyvinyl acetate:

Ten millimoles of tritium gas (10 millimoles=60 milligrams=600 curies) is allowed to react slowly with oxygen in the presence of a palladium catalyst by allowing tritium gas to diffuse through a heated palladium thimble into a flask containing oxygen. Tritium oxide produced by reaction (1) is continuously removed by freezing into a small tube attached to the flask. After completion of reaction (1) the palladium thimble is cooled andunreacted tritium gas is collected on powdered uramum.

Tritiated water contained in said tube is transferred by freezing into a flask containing ten millimoles of acetic anhydride. When the transfer is complete the contents of the flask are warmed to room temperature, and reaction 2) proceeds rapidly to completion, forming tritiated glacial-acetic acid. Tritiated glacial acetic acid reacts with acetylene according to reaction (3) in the presence of a mercuric salt catalyst. The product, tritiated vinyl acetate, is purified by distillation, allowed to polymerize into polyvinyl acetate, then dissolved in amyl acetate. specific activity of the material prepared by this series of reactions is, 60 curies per millimole of vinyl acetate, which can be reduced to any desired specific activity by addition of inactive polyvinyl acetate solution in amyl acetate.

Preparation of a Tritiated Paint Modifier Ten" millimoles of diisooctyl maleate weighing 3.40 grams is dissolved in120 ml. of ethyl acetate contained in The a pressure flask. 300 milligrams of pre-reduced 30% palladium on charcoal catalyst is added to the solution. 20 millimoles of tritium gas (1200 curies) is added to the flask and the contents of the flask including the tritium are shaken until no further takeup of tritium is observed as measured on a mercury manometer. The unreacted tritium (about 600 curies) is collected in a reservoir for future use. The catalyst is removed from solution by filtration, and ethyl acetate is evaporated from the filtrate by a stream of nitrogen. The residue, tritiated diisooctyl succinate, is dissolved in a suitable high-boiling solvent such as xylene, and stored in solution. This material functions as a plasticizer to modify the characteristic of a paint.

Self-luminous paints may be formulated using a tritiated plastic hinder or a non-tritiated plastic binder in conjunction with a tritiated paint modifier, an example of which is tritiated plasticizer. Following are two examples illustrating how such a paint may be prepared.

Preparation of a Self-Luminous Paint Using a T ritiated Plastic Binder A self-luminous paint comprising a tritiated binder can be prepared according to the following procedure. A mixture of 45 grams of zinc orthosilicate; manganese activated phosphor, having an average particle diameter of l to 2 microns, is'mixed together with 5 grams of aluminum stearate in a solution of 50 grams of polyvinyl acetate (not radioactive) in grams of amyl acetate. The amyl acetate functions as a solvent or thinner. This mixture is milled gently for 10 minutes until the mixture is homogeneous. 60 curies of tritiated polyvinyl acetate (1 millimole of material prepared as previously described) is added to the paint mixture and dispersed homogeneously by stirring. 15 grams of a non-radioactive plasticizer, such as dioctyl phthalate, is added if a high initial paint film flexibility is required. The resultant mixture constitutes a self-luminous paint which can be made more viscous by evaporation of amyl acetate or less viscous by addition of more amyl acetate, depending upon the method by which the paint is to be applied.

The brightness of a given thickness of coating Will depend upon the amount of radioactive polyvinyl acetate added per gram of paint. It will also depend upon the coating thickness for thicknesses up to about 20 milligrams/cm? Preparation of a Self-Lumin0us Paint Using a T ritiated Paint Modifier A self-luminous paint comprising a phosphor, and a vehicle therefor comprising a non-tritiated plastic binder and a tritiated plasticizer for the binder can be prepared as follows. A mixture of 45 grams of zinc orthosilicate: manganese activated phosphor having an average particle diameter between 1 and 2 microns is stirred together with 5 grams of aluminum stearate into a solution comprising 33 grams of Acryloid F-lO (manufactured by Rohm & Haas (30., Philadelphia, Pa.) and 25 grams of mineral spirits. Acryloid F-lO is a solution of acrylic resin dissolved in mineral spirits. The additional 25 grams of mineral spirits acts to thin the resin. This mixture is milled gently for 10 minutes until homogeneous. A solution of tritiated plasticizer, diisooctyl succinate-HS, containing 60 curies of tritium and prepared as previously described is added to the paint to make it self-luminous. The radioactive compound must be homogeneously dispersed throughout the paint and this is accomplished by stirring. The viscosity is increased by evaporating the solvent and is decreased by adding solvent.

The brightness'of the self-luminous coatings with this paint can be increased by increasing the number of curies of tritiated plasticizer which is added. Similarly the brightness can be decreased by decreasing the number of curies added. The brightness is also dependent upon the coating thickness up to thicknesses of about 20 milligrams persquare centimeter.

One of the advantages of the present invention resides in the fact that it can be applied to paints comprising various plastic binders and paint modifiers. Following is a list of plastic binders which can be tritiated to produce a self-luminous paint: acrylic resins, alkyd resins, cellulose acetate, ethyl cellulose, hydroxyethyl cellulose, phenol formaldehyde resins, polyester resins, polystyrene resins, urea formaldehyde resins, vinyl resins, polyvinyl resins, polyvinyl alcohol.

The foregoing plastics may comprise all or part of the vehicle of the paint, excluding the volatile constituents thereof. Following is a list of plasticizers which can be tritiated for the purposes of the present invention: dioctyl adipate, diisooctyl azelate, polyethyleneglycol dibenzoate, tri-n-butyl citrate, glycerol tributyrate, glycerol monolaurate, arnyl oleate, di-n-octyl phthalate, dibutyl sebacate, amyl stearate, dibutyl succinate, dibutyl tartrate.

The foregoing list of plastics and plasticizers is not to be construed as limiting the invention but are presented by way of example only. The primary requisite of this invention is that the paint comprise a non-volatile hydrogenous material which may function either as a binder or as a paint modifier and which is tritiated.

Tritiating the paint modifier is just as eifective as tritiating the plastic binder. A self-luminous tritium paint is eflicient only if the tritiated compound is homogeneously dispersed throughout the paint. Because a plasticizer or other paint modifier must be compatible with the plastic binder, it readily disperses uniformly throughout the binder. Accordingly, if the paint modifier is tritiated the radioactivity will be uniformly distributed in the paint.

Tritium and tritium paints have many advantages over radium and radium paints. One of the advantages of using tritium is that it is especially suitable as a radiation source for exciting phosphors. It has very low penetrating power, the beta radiation emitted therefrom having a penetration power of about 0.8 milligram per square centimeter. In most plastics this corresponds to a linear range of approximately 8 (10- cm. In addition it is readily available at a relatively low cost. Tritium is about 100,000 times less hazardous than radium if absorbed by the human body and no expensive shielding is required in preparing, handling and using the paint. Moreover, the beta radiations from tritium do not result in phosphor destruction so that the rate of loss of brightness of tritiated paints is essentially the same as the rate of radioactive decay of tritium, about 6% per year.

Another advantage of tritium paints is that they can be made in various colors more efiectively than radium paints. If it is desired to make a self-luminous paint in a color other than the conventional green but with the same brightness, it would be necessary, due to the human eyes lower response to colors other than green, to increase the concentration of radioactivity in the paint. However, when this is done with radium, it is found that the rate of destruction of the phosphor by the radium is increased tremendously, resulting in an unstable paint having a short useful life.

In the case of tritium, however, no such adverse result is produced. When the concentration of tritium is increased, the rate of loss of brightness remains substantially the same. Hence paints in colors other than green in brightnesses perceptible to the human eye are possible under the present invention. Similarly, it is possible to increase the brightness of green tritium paints by adding more radioactivity without affecting the stability thereof. By the present invention it is possible to produce green paints having a brightness to 30 times as great as those paints employing radium compounds, and still not in-,

crease the rate of loss of brightness. 7

Another advantage of tritium paints resides in their adaptability to application by silk screening. Due to the hazards of its radiations, radium paint must be handled in small concentrations. Thus, for example, it is the practice to silk screen only one clock dial at a time.

Naturally this increases the cost of manufacturing the dial. With tritium there is no such danger and it is possible to silk screen clock dials in quantity without hazard to personnel. This saving in time reduces the cost of producing clock dials.

Still a further advantage of the present invention is that the radioactive material is a component part of the paint vehicle. Because the plastic binder and the paint modifier, either of which may be modified, are non-volatile, there is no loss of radioactivity to the atomsphere. In this connection it is to be noted that if the plastic binder is tritiated, it must not be in the monomer state since monomers generally are volatile. The plastic binder, if tritiated, must be at least partly polymerized so as to have low volatility. It is recognized that where the paint modifier is tritiated, the plastic binder may be in a volatile state since evaporation of binder will not produce any loss of radioactivity, the tritiated modifier being non-volatile. Nevertheless, the loss of any binder at all is to be avoided for reasons of economy. Accordingly, in practice the embodiments of the present invention will comprise a plastic binder which is at least partially polymerized, that is, in a non-volatile state, regardless of whether the binder or the paint modifier is tritiated, and a solvent or thinner for the binder.

Obviously many modifications and variations of the present invention are possible in the light of the above teachings. Therefore, it is to be understood that the invention is not limited in its application to the details specifically described hereinabove and that within the scope of the appended claims it may be practiced otherwise than as specifically described.

We claim:

I. A self-luminous paint consisting essentially of an inorganic phosphorescent material in particle form and a tritiated hydrogenous nonvolatile polymerized organic plastic dispersed uniformly in a volatile solvent for said plastic, said plastic selected from the group consisting of acrylic resins, alkyd resins, cellulose acetate, ethyl cellulose, hydroxy-ethyl cellulose, phenol formaldehyde resins, polyester resins, polystyrene resins, urea formaldehyde resins and vinyl resins, the average distance between adjacent phosphorescent particles being less than about 3 microns when said solvent is removed.

2. A composition of matter consisting essentially of an inorganic phosphorescent material in particle form embedded in a tritiated organic polymer plastic, said plastic selected from the group consisting of acrylic resins, alkyd resins, cellulose acetate, ethyl cellulose, hydroxy-ethyl cellulose, phenol formaldehyde resins, polyester resins, polystyrene resins, urea formaldehyde resins and vinyl resins, the average distance between adjacent phosphorescent particles being less than about 3 microns.

3. A self-luminous paint consisting essentially of an inorganic phosphorescent material in particle form dispersed in a tritiated organic plastic selected from the group consisting of acrylic resins, alkyd resins, cellulose acetate, ethyl cellulose, hydroxyethyl cellulose, phenol formaldehyde resins, polyester resins, polystyrene resins, urea formaldehyde resins and vinyl resins, the average distance between adjacent phosphorescent particles being less than about 3 microns.

References Cited in the file of this patent UNITED STATES PATENTS 2,039,734 Meder May 5, 1936 2,749,251 Shapiro June 5, 1956 FOREIGN PATENTS 646,414 Great Britain Nov. 22, 1950 OTHER REFERENCES Luminous and Fluorescent Paints, by Dept. of Comm. Nat. Bureau of Standards, Sept. 9, 1942; Circular Letter LC 703 and 678.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2039734 *Feb 23, 1933May 5, 1936Ig Farbenindustrie AgNew compositions of matter containing luminous substances
US2749251 *Oct 29, 1953Jun 5, 1956Tracerlab IncSource of luminosity
GB646414A * Title not available
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3147243 *Aug 8, 1960Sep 1, 1964Continental Oil CoRadioactive polymers
US3238139 *Apr 25, 1961Mar 1, 1966Trilux Lenze Gmbh & Co KgMethod of making a tritiated selfluminescent body
US3325420 *Apr 15, 1964Jun 13, 1967Westo Gmbh Fabrik Fur ChemischTritium-activated luminous pigments
US3342743 *Mar 19, 1965Sep 19, 1967Lab For Electronics IncProcess of preparing a zinc sulfide powder coated with tritiated polystyrene
US3366573 *Oct 24, 1965Jan 30, 1968Canrad Prec Ind IncCoated phosphor having radioisotope dispersed therein and method of preparation
US3436242 *Oct 13, 1965Apr 1, 1969Fluckinger & CieMethod of making luminescent dial with resin and fluorescent top layer
US4889660 *Dec 24, 1987Dec 26, 1989Battelle Memorial InstituteRadioluminescent light sources, tritium containing polymers, and methods for producing the same
US5008579 *Mar 3, 1989Apr 16, 1991E. F. Johnson Co.Light emitting polymer electrical energy source
US5100968 *Dec 21, 1989Mar 31, 1992Battelle Memorial InstituteTritium containing polymers having a polymer backbone substantially void of tritium
US5124610 *Mar 4, 1991Jun 23, 1992E. F. Johnson CompanyTritiated light emitting polymer electrical energy source
US5235232 *Sep 4, 1990Aug 10, 1993E. F. Johnson CompanyAdjustable-output electrical energy source using light-emitting polymer
US5237233 *Sep 4, 1990Aug 17, 1993E. F. Johnson CompanyOptoelectronic active circuit element
US7234498Apr 6, 2004Jun 26, 2007The Goodyear Tire & Rubber CompanySelf-luminescent pneumatic tire
US20040238782 *May 12, 2004Dec 2, 2004Tomio InoueElectric characteristic modifying material
US20040238802 *May 12, 2004Dec 2, 2004Tomio InoueCombustion promoting material
US20050217782 *Apr 6, 2004Oct 6, 2005Giorgio AgostiniSelf-luminescent pneumatic tire
US20130040765 *Aug 8, 2011Feb 14, 2013Teno DeMont MylesLuminous attachable basketball training device
EP0387624A1 *Mar 1, 1990Sep 19, 1990E.F. Johnson CompanyLight emitting polymer electrical energy source
WO1990010938A1 *Feb 26, 1990Sep 20, 1990E.F. Johnson CompanyLight emitting polymer electrical energy source
Classifications
U.S. Classification252/646
International ClassificationC09K11/00, C09D5/22, C09K11/04
Cooperative ClassificationC09K11/04, C09D5/22
European ClassificationC09K11/04, C09D5/22