[go: up one dir, main page]

US3565815A - Phosphor containing plastic polystyrene - Google Patents

Phosphor containing plastic polystyrene Download PDF

Info

Publication number
US3565815A
US3565815A US694082A US3565815DA US3565815A US 3565815 A US3565815 A US 3565815A US 694082 A US694082 A US 694082A US 3565815D A US3565815D A US 3565815DA US 3565815 A US3565815 A US 3565815A
Authority
US
United States
Prior art keywords
polystyrene
phthalate
percent
product
wax
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US694082A
Inventor
Alexander C Christy
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Industrial Manufacturing Co Inc
Original Assignee
Industrial Manufacturing Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Industrial Manufacturing Co Inc filed Critical Industrial Manufacturing Co Inc
Application granted granted Critical
Publication of US3565815A publication Critical patent/US3565815A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/10—Esters; Ether-esters
    • C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02—Homopolymers or copolymers of hydrocarbons
    • C08L25/04—Homopolymers or copolymers of styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06—Waxes
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S273/00—Amusement devices: games
    • Y10S273/02—Styrene
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S273/00—Amusement devices: games
    • Y10S273/24—Luminescent, phosphorescent
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00—Stock material or miscellaneous articles
    • Y10S428/913—Material designed to be responsive to temperature, light, moisture

Definitions

  • a moldable plastic product comprising polystyrene or copolymers of polystyrene such as the vinyls including, for example, vinyl chloride, vinyl acetate, vinyl butyral, vinylidene chloride, acrylonitrile, butadiene, alpha or betamethyl styrene and maleic anhydride, and others, at least 45 percent by weight polystyrene of a phthalate plasticizer such as the alkyl, aryl, alkyl aryl, dialkyl and diaryl phthalates and in particular the dioctyl' phthalates, at least 3 percent by weight polystyrene or any wax such as natural or synthetic animal, vegetable or mineral waxes; preferred are the paraffin waxes containing paraffinic hydrocarbons having a carbon content of at least 16 carbon atoms, and at least .001 percent by weight polystyrene of an electroluminescent, fluorescent or phosphorescent
  • the present invention relates generally to a moldable plastic polystyrene. More particularly, the present invention relates to a useful amusement product of polystyrene which can be molded shaped and has adhesive properties and can be made to glow in the dark.
  • Amusement devices have been known in the past which include moldable clay, plastic type putty which may be molded and shaped into various forms or extruded into unusual designs in accordance with an exchangeable extrusion plate.
  • Other plastic moldable compositions have been known to have elastic and resilient properties, many of which have met with gerat commercial success in the amusement device and toy manufacturing industry.
  • toys and amusement devices form a part of an industry that is highly competitive.
  • the art reflecting this competition is constantly striving for new products which may attract the eye of the purchaser and provide entertainment for not only chlidren but also adults.
  • Toys and amusement devices which have been found to have met with considerable success in the past are those that provide changeable visible effects. Included in this group are for instance the motor operated toys.
  • Another class that has been found to be particularly attractive to the public are toys of the lighted or illuminated type which, in the dark, provide unusual visual effects.
  • Another object of the present invention is the provision of an amusement device which is moldable and plastic and which can be safely handled by anyone.
  • a further object of the present invention is the provision of a moldable plastic product which may be charged ice by actinic light rays and be made to glow in the dark.
  • Another object of the present invention is to provide a moldable plastic product which can be severed, perforated and shaped and retain a uniform glow in a darkened environment.
  • the present invention is a discovery that the properties and characteristics of polystyrene and also various copolymers of polystyrene can be greatly changed with the addition of a large amount of a phthalate plasticizer, additional desirable characteristics can be obtained by the incorporation of a wax such as a paraffin wax or any animal, vegetable or mineral including the natural or synthetic waxes, and finally this modified polystyrene is capable of receiving phosphors intimately mixed in the product so as to permit the plastic product containing the phosphors to be molded into shapes, severed, or sculptured and at the same time glow in reduced light upon receiving excitation by actinic light rays.
  • a wax such as a paraffin wax or any animal, vegetable or mineral including the natural or synthetic waxes
  • the polystyrene used in accordance with the present invention may be used alone or as a copolymer with a number of the monomers that will copolymerize with styrene.
  • monomers include the vinyls including vinyl chloride, vinyl acetate, vinyl butyral, vinylidene chloride, acrylonitrile, butadiene, alpha or beta-methyl styrene, maleic anhydride, and other vinyl monomers well known to be compatible for copolymerization with polystyrene.
  • plasticizer While it has been known in the past to plasticize polystyrene, the amounts of such plasticizer have been relatively small. In the present invention it has been found that at least 45 percent by weight of the polystyrene alone should be a phthalate plasticizer.
  • esters of phthalic acid that may be utilized are the alkyl, aryl, alkyl aryl, dialkyl and diaryl phthalates.
  • dimethyl phthalate diethyl phthalate, dibutyl phthalate, di-isobutyl phthalate, dihexyl phthalate (n or iso), dimethylisobutylcarbinyl phthalate, butyl octyl phthalate, butyl isodecyl phthalate (decyl butyl phthalate), butyl iso-hexyl phthalate, dioctyl phthalate, di-n-octyl phthalate, dioctyl isophthalate, diisooctyl phthalate, di-isooctyl isophthalate, dicapryl phthalate, di-(Z-ethylhexyl) phthalate, dinonyl phthalate, n-octyln-decyl phthalate, N-decyl/N-octyl phthalate (phthalate of
  • phthalic acid derivatives such as the normal alcohol phthalate, alkoxy alkyl phthalate, for example the dibutoxy ethyl phthalate and fatty acid phthalates may be used in accordance with the present invention provided they are compatible with respect to polystyrene.
  • the alkyl or aryl radicals forming the phthalates in accordance with the present invention should have between 3 and 26 carbon atoms.
  • the amount of the phthalate plasticizer should be at least 45 percent by weight of the polystyrene alone, exclusive of any monomer copolymerized with the polystyrene. Preferably, the amount of plasticizer should be approximately to percent of the weight of the polystyrene.
  • polystyrene will become liquid and when blended with the plasticizer, for instance the di-isooctyl phthalate, the polystyrene and the phthalate appear to take the form of a reaction product.
  • the identity or composition of the product so formed is not clear, nor is it certain that a reaction product does in fact take place. Analytical evidence and the combining quantities however do support the theory that at least a strong physical combination, if not a chemical bonding, takes place between the polystyrene and the phthalate plasticizer.
  • wax such as any natural or synthetic animal, vegetable or mineral wax.
  • Such waxes are desirable to provide supporting means dispersed in the product to enable the user to retain the form or shape produced.
  • the product is found to have desirable shape retention properties.
  • the waxes that may be utilized in accordance with the present invention are any of the animal, vegetable or mineral waxes such as beeswax, candelilla, carnauba, ceresene, insect wax, esparto, Japan, montan, ouricury, ozokerite, parafiin, spermaceti, sugar cane, wool fat.
  • beeswax candelilla
  • carnauba ceresene
  • insect wax esparto
  • Japan montan
  • ouricury ozokerite
  • parafiin spermaceti
  • sugar cane wool fat.
  • paraffin wax which is a mixture of hydrocarbons melting in a range above 43 C. and which is a constituent of petroleum from which it may be distilled.
  • any of the paraflin hydrocarbon series of waxes having a carbon content of at least 16 carbon atoms such as for instance hexadecane, heptadecane, octadecane, etc., may also be used without limitation up through and including the C and greater hydrocarbons such as hepta- Contane.
  • the mixtures as well as isomers of the parafimic hydrocarbons are also useful for the purposes of this invention.
  • the amount of wax may vary from about to 45 percent of the polystyrene.
  • composition including the polystyrene, the plasticizer and the wax is usable without more as a moldable product. However, it does not have the unique characteristics of being able to radiate visual effects in reduced light. It has now been discovered that when a phosphor in an amount between .001 percent of the polystyrene is added to the plastic product that the unusual visual effects can be attained. Electroluminescent, fluorescent, and phosphorescent phosphors generally described as P P may be used to achieve the visual effects of the present invention.
  • any of the inorganic phosphors of the sulfide or oxide type may be usable as long as they are excited by sources of actinic radiation.
  • sources of actinic radiation Preferably those which are excited by sources readily available such as visible light or ultraviolet radiation are the most suitable. Since the phosphors vary considerably in the color of the radiation emitted, it is possible to use particular phosphors for obtaining almost any color.
  • the styrene is heated to a liquid state which is between 375 and 465 F. (the melting temperature may be correspondingly varied in accordance with the identity of the copolymer).
  • the phthalate such as di-isooctyl phthalate is blended and mixed with the polystyrene. It is believed that at this elevated temperature the polystyrene molecules are excited to the extent that the spacing between the molecules is increased such that the phthalate molecules are enabled to take a position betwen the polystyrene molecules.
  • the preferred temperature is 420 F.
  • the wax is added at the time after the phthalate plasticizer is completely blended. Thereafter the phosphors are added to provide the necessary glow pr perties.
  • the product may be stretched, severed, sculptured, molded in any manner and, upon activation from normal light present, the contained phosphor will provide a glow in the dark. It has further been found that irrespective of what shape or how stretched or molded the product has been, the glow will be uniform and homogeneous in appearance. More importantly, the glow will be of substantial magnitude, far greater than could be expected of phosphors on the surface. Depending upon the phosphor used, the glow will be retained for several minutes up to an hour or more.
  • the glow is not attained solely by surface phosphors but, due to the important radiation transmitting and almost transparent nature of the polystyrene phthalate and wax matrix, there is substantially no obstruction to the passage of the phosphor radiation from all contained phosphors through the matrix to obtain the full measure of the glow.
  • oleaginous materials such as Vaseline or any oil fats may be added if desired to provide purely a smoother, softer feel to the product.
  • the addition of the Vaseline or other oleaginous material is not essential to the performance of the product.
  • the product of the present invention will act as an image retaining means when impressed upon a surface such as paper which has been written upon with ball point pen or soft pencil and will transfer a portion of this image to another surface including the human skin or paper when impressed upon this other surface.
  • the product of the present invention is also nontoxic to humans and does not harden with nonuse. Shelf life has been found to be outstanding in tests performed to date.
  • composition of the present invention may be formed in the shape of pellets or bullets and, if propelled as if shot from a gun in the dark, the bullets or pellets would glow and have the appearance of tracer or light bullets.
  • a phthalate plasticizer selected from the group consisting of alkyl radical containing 3-26 carbon atoms, cycloalkyl, aryl, alkoxy alkyl, alkyl aryl, alcohol, fatty acid, dialkyl and diaryl phthalates, and including at least 3 percent up to 50% by weight polystyrene of a wax selected from the group consisting of
  • polystyrene is in the form of a copolymer and wherein at least percent of the copolymer is polystyrene.
  • plasticizer is selected from the group of sulfide and oxide phosphors.
  • plasticizer is a dioctyl phthalate and is present in the amount of 90 to 110 percent of the polystyrene.
  • the product of claim 1 including a dioctyl phthalate as the plasticizer, a wax having a carbon content 16-70, and a phosphor selected from the group of sulfide and oxide phosphors.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A MOLDABLE PLASTIC PRODUCT COMPRISING POLYSTYRENE OR COPOLYMERS OF POLYSTYRENE SUCH AS THE VINYLS INCLUDING FOR EXAMPLE, VINYL CHLORIDE, VINYL ACETATE, VINYL BUTYRAL, VINYLIDENE CHLORIDE, ACRYLONITRILE, BUTADIENE, ALPHA OR BETAMETHYL STYRENE AND MALEIC ANHYDRIDE, AND OTHERS, AT LEAST 45 PERCENT BY WEIGHT POLYSTYRENE OF A PHTHALATE PLASTICIZER SUCH AS THE ALKYL, ARYL, ALKYL ARYL, DIALKYL AND DIARYL PHTHALATES AND IN PARTICULAR THE DIOCTYL PHTHALATES, AT LEAST 3 PERCENT BY WEIGHT POLYSTYRENE OR ANY WAX SUCH AS NATURAL OR SYNTHETIC ANIMAL, VEGETABLE OR MINERAL WAXES; PREFERRED ARE THE PARAFFIN WAXES CONTAINING PARAFFINIC HYDROCARBONS HAVING A CARBON CONTENT OF AT LEAST 16 CARBON ATOMS, AND AT LEAST .001 PERCENT BY WEIGHT POLYSTYRENE OF AN ELECTROLUMINESCENT, FLUORESCENT OR PHOSPHORESCENT PHOSPHOR SUCH AS THE P1-P30 TYPE PHOSPHORS WHICH INCLUDE THE SULFIDE AND OXIDE PHOSPHORS.

Description

United States Patent 3,565,815 PHOSPHOR CONTAINING PLASTIC POLYSTYRENE Alexander C. Christy, Morgantown, W. Va., assignor to Industrial Manufacturing Company, Inc., Morgantown, W. Va., a corporation of West Virginia N0 Drawing. Filed Dec. 28, 1967, Ser. No. 694,082 Int. Cl. A6311 33/00; C08c 1 1 70; C09k N00 US. Cl. 252-3013 10 Claims ABSTRACT OF THE DISCLOSURE A moldable plastic product comprising polystyrene or copolymers of polystyrene such as the vinyls including, for example, vinyl chloride, vinyl acetate, vinyl butyral, vinylidene chloride, acrylonitrile, butadiene, alpha or betamethyl styrene and maleic anhydride, and others, at least 45 percent by weight polystyrene of a phthalate plasticizer such as the alkyl, aryl, alkyl aryl, dialkyl and diaryl phthalates and in particular the dioctyl' phthalates, at least 3 percent by weight polystyrene or any wax such as natural or synthetic animal, vegetable or mineral waxes; preferred are the paraffin waxes containing paraffinic hydrocarbons having a carbon content of at least 16 carbon atoms, and at least .001 percent by weight polystyrene of an electroluminescent, fluorescent or phosphorescent phosphor such as the P P type phosphors which include the sulfide and oxide phosphors.
The present invention relates generally to a moldable plastic polystyrene. More particularly, the present invention relates to a useful amusement product of polystyrene which can be molded shaped and has adhesive properties and can be made to glow in the dark.
Amusement devices have been known in the past which include moldable clay, plastic type putty which may be molded and shaped into various forms or extruded into unusual designs in accordance with an exchangeable extrusion plate. Other plastic moldable compositions have been known to have elastic and resilient properties, many of which have met with gerat commercial success in the amusement device and toy manufacturing industry.
It is well known that the toys and amusement devices form a part of an industry that is highly competitive. The art reflecting this competition is constantly striving for new products which may attract the eye of the purchaser and provide entertainment for not only chlidren but also adults. Toys and amusement devices which have been found to have met with considerable success in the past are those that provide changeable visible effects. Included in this group are for instance the motor operated toys. Another class that has been found to be particularly attractive to the public are toys of the lighted or illuminated type which, in the dark, provide unusual visual effects.
Until the present invention, it has not been known to incorporate visual effects in the dark in a moldable plastic material. Moreover, in the toy and amusement field it is necessary to also provide maximum safety precautions against physical hazards. Thus, for a successful commercial toy or amusement device it is important to provide for the safe use of the toy.
Accordingly, it is the principal object of the present invention to provide a moldable plastic product which provides visual effects in a darkened environment.
Another object of the present invention is the provision of an amusement device which is moldable and plastic and which can be safely handled by anyone.
A further object of the present invention is the provision of a moldable plastic product which may be charged ice by actinic light rays and be made to glow in the dark.
Another object of the present invention is to provide a moldable plastic product which can be severed, perforated and shaped and retain a uniform glow in a darkened environment.
The present invention is a discovery that the properties and characteristics of polystyrene and also various copolymers of polystyrene can be greatly changed with the addition of a large amount of a phthalate plasticizer, additional desirable characteristics can be obtained by the incorporation of a wax such as a paraffin wax or any animal, vegetable or mineral including the natural or synthetic waxes, and finally this modified polystyrene is capable of receiving phosphors intimately mixed in the product so as to permit the plastic product containing the phosphors to be molded into shapes, severed, or sculptured and at the same time glow in reduced light upon receiving excitation by actinic light rays.
The polystyrene used in accordance with the present invention may be used alone or as a copolymer with a number of the monomers that will copolymerize with styrene. Among such monomers are the vinyls including vinyl chloride, vinyl acetate, vinyl butyral, vinylidene chloride, acrylonitrile, butadiene, alpha or beta-methyl styrene, maleic anhydride, and other vinyl monomers well known to be compatible for copolymerization with polystyrene.
It has been found that the amount of copolymerization, if any, is not critical or necessary, but that the desirable qualities of the present invention are more noticeable when the styrene monomer represents at least percent by weight of the copolymer.
While it has been known in the past to plasticize polystyrene, the amounts of such plasticizer have been relatively small. In the present invention it has been found that at least 45 percent by weight of the polystyrene alone should be a phthalate plasticizer. Among the esters of phthalic acid that may be utilized are the alkyl, aryl, alkyl aryl, dialkyl and diaryl phthalates. Within this broad classification may be listed the following: dimethyl phthalate, diethyl phthalate, dibutyl phthalate, di-isobutyl phthalate, dihexyl phthalate (n or iso), dimethylisobutylcarbinyl phthalate, butyl octyl phthalate, butyl isodecyl phthalate (decyl butyl phthalate), butyl iso-hexyl phthalate, dioctyl phthalate, di-n-octyl phthalate, dioctyl isophthalate, diisooctyl phthalate, di-isooctyl isophthalate, dicapryl phthalate, di-(Z-ethylhexyl) phthalate, dinonyl phthalate, n-octyln-decyl phthalate, N-decyl/N-octyl phthalate (phthalate of mixed N-alcohols), octyl decyl phthalate (isooctyl isodecyl phthalate) (isooctyl decyl phthalate), di-decyl phthalate (di-isodecyl phthalate), decyltridecyl phthalate, ditridecyl phthalate, octyl fatty phthalic ester, ethylhexyl decyl phthalate, butyl-ethylhexyl phthalate, diallyl hthalate, butyl cyclohexyl phthalate, butyl benzy phthalate (BBP), di(methylcyclohexyl) phthalate, diphenyl phthalate, 2- ethyl hexyl isodecyl phthalate. Other phthalic acid derivatives such a the normal alcohol phthalate, alkoxy alkyl phthalate, for example the dibutoxy ethyl phthalate and fatty acid phthalates may be used in accordance with the present invention provided they are compatible with respect to polystyrene.
The alkyl or aryl radicals forming the phthalates in accordance with the present invention should have between 3 and 26 carbon atoms. The amount of the phthalate plasticizer should be at least 45 percent by weight of the polystyrene alone, exclusive of any monomer copolymerized with the polystyrene. Preferably, the amount of plasticizer should be approximately to percent of the weight of the polystyrene.
At elevated temperature of approximately 375 to 465 F. and preferably around 420 F. polystyrene will become liquid and when blended with the plasticizer, for instance the di-isooctyl phthalate, the polystyrene and the phthalate appear to take the form of a reaction product. The identity or composition of the product so formed is not clear, nor is it certain that a reaction product does in fact take place. Analytical evidence and the combining quantities however do support the theory that at least a strong physical combination, if not a chemical bonding, takes place between the polystyrene and the phthalate plasticizer.
In order to obtain shape retention properties of the product produced from the combination of the polystyrene and the phthalate plasticizer and also to minimize cold flow, it has been found to be important to add a wax such as any natural or synthetic animal, vegetable or mineral wax. Such waxes are desirable to provide supporting means dispersed in the product to enable the user to retain the form or shape produced. When such waxes are used in an amount between 3 and 50 percent by weight of the polystyrene, the product is found to have desirable shape retention properties.
The waxes that may be utilized in accordance with the present invention are any of the animal, vegetable or mineral waxes such as beeswax, candelilla, carnauba, ceresene, insect wax, esparto, Japan, montan, ouricury, ozokerite, parafiin, spermaceti, sugar cane, wool fat. The
preferred wax is paraffin wax which is a mixture of hydrocarbons melting in a range above 43 C. and which is a constituent of petroleum from which it may be distilled. Additionally, any of the paraflin hydrocarbon series of waxes having a carbon content of at least 16 carbon atoms such as for instance hexadecane, heptadecane, octadecane, etc., may also be used without limitation up through and including the C and greater hydrocarbons such as hepta- Contane. The mixtures as well as isomers of the parafimic hydrocarbons are also useful for the purposes of this invention. Preferably, the amount of wax may vary from about to 45 percent of the polystyrene.
The composition including the polystyrene, the plasticizer and the wax is usable without more as a moldable product. However, it does not have the unique characteristics of being able to radiate visual effects in reduced light. It has now been discovered that when a phosphor in an amount between .001 percent of the polystyrene is added to the plastic product that the unusual visual effects can be attained. Electroluminescent, fluorescent, and phosphorescent phosphors generally described as P P may be used to achieve the visual effects of the present invention.
Typical, though by no means exhaustive, of the types of phosphors that may be used are those such as CaSrSzBi; ZnCdSzCuzMg; siO zMg; CdS:Cu; ZnO; ZnS:Ni:Mn; ZnS:Cu:Mn; ZnSzCuzAg; (Zn, Cd) SzAg. In general, any of the inorganic phosphors of the sulfide or oxide type may be usable as long as they are excited by sources of actinic radiation. Preferably those which are excited by sources readily available such as visible light or ultraviolet radiation are the most suitable. Since the phosphors vary considerably in the color of the radiation emitted, it is possible to use particular phosphors for obtaining almost any color.
In order to form the product of the invention, the styrene is heated to a liquid state which is between 375 and 465 F. (the melting temperature may be correspondingly varied in accordance with the identity of the copolymer). When the polystyrene is liquefied the phthalate such as di-isooctyl phthalate is blended and mixed with the polystyrene. It is believed that at this elevated temperature the polystyrene molecules are excited to the extent that the spacing between the molecules is increased such that the phthalate molecules are enabled to take a position betwen the polystyrene molecules. The preferred temperature is 420 F. The wax is added at the time after the phthalate plasticizer is completely blended. Thereafter the phosphors are added to provide the necessary glow pr perties.
4 EXAMPLE I 325 grams of polystyrene were heated to 420 F. and 400 grams of di-isooctyl phthalate were added and blended with agitation. Upon completion of the blending, 100 grams of paraffin wax and 35 grams of zinc sulfide, copper activated (ZnSICu) phosphor was added. Agitation is continued until a homogeneous product is obtained.
Upon cooling, it was found that the product may be stretched, severed, sculptured, molded in any manner and, upon activation from normal light present, the contained phosphor will provide a glow in the dark. It has further been found that irrespective of what shape or how stretched or molded the product has been, the glow will be uniform and homogeneous in appearance. More importantly, the glow will be of substantial magnitude, far greater than could be expected of phosphors on the surface. Depending upon the phosphor used, the glow will be retained for several minutes up to an hour or more.
One of the reasons for the magnitude of the glow has been found to be that the phosphors throughout the product contribute to the visible radiation. This is one of the unique facets of the present invention that the glow is not attained solely by surface phosphors but, due to the important radiation transmitting and almost transparent nature of the polystyrene phthalate and wax matrix, there is substantially no obstruction to the passage of the phosphor radiation from all contained phosphors through the matrix to obtain the full measure of the glow.
To the above composition, oleaginous materials such as Vaseline or any oil fats may be added if desired to provide purely a smoother, softer feel to the product. The addition of the Vaseline or other oleaginous material is not essential to the performance of the product.
Another of the unique characteristics of the product of the present invention is that the product will act as an image retaining means when impressed upon a surface such as paper which has been written upon with ball point pen or soft pencil and will transfer a portion of this image to another surface including the human skin or paper when impressed upon this other surface.
The product of the present invention is also nontoxic to humans and does not harden with nonuse. Shelf life has been found to be outstanding in tests performed to date.
It is also contemplated that as a toy or amusement device, the composition of the present invention may be formed in the shape of pellets or bullets and, if propelled as if shot from a gun in the dark, the bullets or pellets would glow and have the appearance of tracer or light bullets.
From the foregoing detailed description it will be evident that there are a number of changes, adaptations and modifications of the present invention which come within the province of those skilled in the art. However, it is intended that all such variations not departing from the spirit of the invention be considered as within the scope thereof as limited solely by the appended claims.
What is claimed is:
1. A moldable plastic product formed from polystyrene and at least 45 percent by weight polystyrene of a phthalate plasticizer selected from the group consisting of alkyl radical containing 3-26 carbon atoms, cycloalkyl, aryl, alkoxy alkyl, alkyl aryl, alcohol, fatty acid, dialkyl and diaryl phthalates, and including at least 3 percent up to 50% by weight polystyrene of a wax selected from the group consisting of natural and synthetic animal, vegetable and mineral waxes, and at least .001 percent by weight polystyrene of a phosphor.
2. The product of claim 1 wherein polystyrene is in the form of a copolymer and wherein at least percent of the copolymer is polystyrene.
3. The product of claim 1 wherein the plasticizer is selected from the group of sulfide and oxide phosphors.
4. The product of claim 1 wherein the wax is a paraffin wax.
5. The product of claim 1 wherein the wax is a solid paraflinic hydrocarbon having a carbon content from 16-70.
6. The product of claim 1 wherein the plasticizer is a dioctyl phthalate and is present in the amount of 90 to 110 percent of the polystyrene.
7. The product of claim 4 whereinthe paraffin is present in the amount of 25 to 40 percent of the polystyrene.
8. The product of claim 1 including a dioctyl phthalate as the plasticizer, a wax having a carbon content 16-70, and a phosphor selected from the group of sulfide and oxide phosphors.
9. The product of claim 1 wherein the plasticizer is present in the amount of 90-110 percent by weight of the polystyrene and the wax is present in an amount of 25 to 40 percent by weight of the polystyrene.
10. The product of claim 9 wherein the wax is a parafiin wax.
References Cited TOBIAS E. LEVOW, Primary Examiner A. P. DEMERS, Assistant Examiner US. Cl. XJR.
US694082A 1967-12-28 1967-12-28 Phosphor containing plastic polystyrene Expired - Lifetime US3565815A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US69408267A 1967-12-28 1967-12-28

Publications (1)

Publication Number Publication Date
US3565815A true US3565815A (en) 1971-02-23

Family

ID=24787329

Family Applications (1)

Application Number Title Priority Date Filing Date
US694082A Expired - Lifetime US3565815A (en) 1967-12-28 1967-12-28 Phosphor containing plastic polystyrene

Country Status (1)

Country Link
US (1) US3565815A (en)

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3902722A (en) * 1973-07-05 1975-09-02 John A Skillern Elastic band
US3996176A (en) * 1972-03-08 1976-12-07 Zareh Lorenian Method of manufacturing shaped members of synthetic thermoplastic materials free of softeners
US4525295A (en) * 1980-05-27 1985-06-25 Adver-Togs, Inc. Method of and composition for producing glow printing
US4629583A (en) * 1985-06-11 1986-12-16 Jones And Vining, Incorporated Phosphorescent polymer-containing compositions and articles made therefrom
US4640797A (en) * 1985-06-11 1987-02-03 Jones And Vining, Incorporated Phosphorescent polymer-containing compositions and articles made therefrom
US4735660A (en) * 1987-06-26 1988-04-05 Mattel, Inc. Cross-linked gel modeling composition
WO1991015553A1 (en) * 1990-04-05 1991-10-17 William Grandmont Phosphorescent marking material
US5116533A (en) * 1990-04-05 1992-05-26 William Grandmont Phosphorescent marking material
US5157063A (en) * 1991-11-21 1992-10-20 Wetherell Joseph J Elastic modeling paste
US5258068A (en) * 1992-01-21 1993-11-02 Mattel, Inc. Play material composition
US5330195A (en) * 1989-12-15 1994-07-19 Sports Glow, Inc. Glow-in-the-dark-golf ball making method
US5695696A (en) * 1994-12-19 1997-12-09 Interface, Inc. Method of forming a floor mat with phosphorescent border
US5876995A (en) * 1996-02-06 1999-03-02 Bryan; Bruce Bioluminescent novelty items
US5916949A (en) * 1997-08-18 1999-06-29 Mattel, Inc. Moldable compositions and method of making the same
US6117363A (en) * 1997-03-10 2000-09-12 Sony Corporation Method for producing light-emitting material
US6232107B1 (en) 1998-03-27 2001-05-15 Bruce J. Bryan Luciferases, fluorescent proteins, nucleic acids encoding the luciferases and fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items
US6247995B1 (en) 1996-02-06 2001-06-19 Bruce Bryan Bioluminescent novelty items
US6312782B1 (en) * 1991-03-18 2001-11-06 Rochelle L. Goldberg Discreet shaped colored polymeric objects in a transparent or translucent matrix
US20010045647A1 (en) * 1996-09-20 2001-11-29 Osram Opto Semiconductors Gmbh & Co., Ohg Method of producing a wavelength-converting casting composition
US20030092098A1 (en) * 2000-03-15 2003-05-15 Bruce Bryan Renilla reniformis fluorescent proteins, nucleic acids encoding the fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items
US6881781B1 (en) 2003-12-01 2005-04-19 The Wingum Company Modeling compound
US20050127385A1 (en) * 1996-06-26 2005-06-16 Osram Opto Semiconductors Gmbh & Co., Ohg, A Germany Corporation Light-radiating semiconductor component with a luminescence conversion element
US20080150173A1 (en) * 2005-01-19 2008-06-26 Ivan To Method For Fabricating Luminescent Articles
US10274291B2 (en) 2015-03-04 2019-04-30 Kryptolight Targets Llc Luminescent archery target

Cited By (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3996176A (en) * 1972-03-08 1976-12-07 Zareh Lorenian Method of manufacturing shaped members of synthetic thermoplastic materials free of softeners
US3902722A (en) * 1973-07-05 1975-09-02 John A Skillern Elastic band
US4525295A (en) * 1980-05-27 1985-06-25 Adver-Togs, Inc. Method of and composition for producing glow printing
US4629583A (en) * 1985-06-11 1986-12-16 Jones And Vining, Incorporated Phosphorescent polymer-containing compositions and articles made therefrom
US4640797A (en) * 1985-06-11 1987-02-03 Jones And Vining, Incorporated Phosphorescent polymer-containing compositions and articles made therefrom
US4735660A (en) * 1987-06-26 1988-04-05 Mattel, Inc. Cross-linked gel modeling composition
US5330195A (en) * 1989-12-15 1994-07-19 Sports Glow, Inc. Glow-in-the-dark-golf ball making method
WO1991015553A1 (en) * 1990-04-05 1991-10-17 William Grandmont Phosphorescent marking material
US5116533A (en) * 1990-04-05 1992-05-26 William Grandmont Phosphorescent marking material
US6312782B1 (en) * 1991-03-18 2001-11-06 Rochelle L. Goldberg Discreet shaped colored polymeric objects in a transparent or translucent matrix
US5157063A (en) * 1991-11-21 1992-10-20 Wetherell Joseph J Elastic modeling paste
US5258068A (en) * 1992-01-21 1993-11-02 Mattel, Inc. Play material composition
US5695696A (en) * 1994-12-19 1997-12-09 Interface, Inc. Method of forming a floor mat with phosphorescent border
US5876995A (en) * 1996-02-06 1999-03-02 Bryan; Bruce Bioluminescent novelty items
US6113886A (en) * 1996-02-06 2000-09-05 Bruce Bryan Bioluminescent novelty items
US20060053505A1 (en) * 1996-02-06 2006-03-09 Bruce Bryan Bioluminescent novelty items
US6152358A (en) * 1996-02-06 2000-11-28 Bruce Bryan Bioluminescent novelty items
US6247995B1 (en) 1996-02-06 2001-06-19 Bruce Bryan Bioluminescent novelty items
US7151283B2 (en) 1996-06-26 2006-12-19 Osram Gmbh Light-radiating semiconductor component with a luminescence conversion element
US7345317B2 (en) 1996-06-26 2008-03-18 Osram Gmbh Light-radiating semiconductor component with a luminescene conversion element
US9196800B2 (en) 1996-06-26 2015-11-24 Osram Gmbh Light-radiating semiconductor component with a luminescence conversion element
US7629621B2 (en) 1996-06-26 2009-12-08 Osram Gmbh Light-radiating semiconductor component with a luminescence conversion element
US20080149958A1 (en) * 1996-06-26 2008-06-26 Ulrike Reeh Light-Radiating Semiconductor Component with a Luminescence Conversion Element
US7126162B2 (en) 1996-06-26 2006-10-24 Osram Gmbh Light-radiating semiconductor component with a luminescence conversion element
US7078732B1 (en) 1996-06-26 2006-07-18 Osram Gmbh Light-radiating semiconductor component with a luminescence conversion element
US20050127385A1 (en) * 1996-06-26 2005-06-16 Osram Opto Semiconductors Gmbh & Co., Ohg, A Germany Corporation Light-radiating semiconductor component with a luminescence conversion element
US20050161694A1 (en) * 1996-06-26 2005-07-28 Osram Gmbh Light-radiating semiconductor component with a luminescence conversion element
US20050231953A1 (en) * 1996-06-26 2005-10-20 Osram Gmbh Light-radiating semiconductor component with a luminescence conversion element
US7276736B2 (en) 1996-09-20 2007-10-02 Osram Gmbh Wavelength-converting casting composition and white light-emitting semiconductor component
US7709852B2 (en) 1996-09-20 2010-05-04 Osram Gmbh Wavelength-converting casting composition and light-emitting semiconductor component
US20010045647A1 (en) * 1996-09-20 2001-11-29 Osram Opto Semiconductors Gmbh & Co., Ohg Method of producing a wavelength-converting casting composition
US8071996B2 (en) 1996-09-20 2011-12-06 Osram Gmbh Wavelength-converting casting composition and light-emitting semiconductor component
US20040084687A1 (en) * 1996-09-20 2004-05-06 Osram Opto Semiconductors Gmbh Wavelength-converting casting composition and white light-emitting semiconductor component
US20100176344A1 (en) * 1996-09-20 2010-07-15 Hoehn Klaus Wavelength-converting casting composition and light-emitting semiconductor component
US7235189B2 (en) 1996-09-20 2007-06-26 Osram Gmbh Method of producing a wavelength-converting casting composition
US20070216281A1 (en) * 1996-09-20 2007-09-20 Klaus Hohn Wavelength-converting casting composition and light-emitting semiconductor component
US6117363A (en) * 1997-03-10 2000-09-12 Sony Corporation Method for producing light-emitting material
US5916949A (en) * 1997-08-18 1999-06-29 Mattel, Inc. Moldable compositions and method of making the same
US6232107B1 (en) 1998-03-27 2001-05-15 Bruce J. Bryan Luciferases, fluorescent proteins, nucleic acids encoding the luciferases and fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items
US6436682B1 (en) 1998-03-27 2002-08-20 Prolume, Ltd. Luciferases, fluorescent proteins, nucleic acids encoding the luciferases and fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items
US20030092098A1 (en) * 2000-03-15 2003-05-15 Bruce Bryan Renilla reniformis fluorescent proteins, nucleic acids encoding the fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items
US20050272111A1 (en) * 2000-03-15 2005-12-08 Bruce Bryan Renilla reniformis fluorescent proteins, nucleic acids encoding the fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items
US7109315B2 (en) 2000-03-15 2006-09-19 Bruce J. Bryan Renilla reniformis fluorescent proteins, nucleic acids encoding the fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items
US6881781B1 (en) 2003-12-01 2005-04-19 The Wingum Company Modeling compound
US20080150173A1 (en) * 2005-01-19 2008-06-26 Ivan To Method For Fabricating Luminescent Articles
US10274291B2 (en) 2015-03-04 2019-04-30 Kryptolight Targets Llc Luminescent archery target

Similar Documents

Publication Publication Date Title
US3565815A (en) Phosphor containing plastic polystyrene
US3847865A (en) Use of alumina trihydrate in a polymethyl methacrylate article
GB1529603A (en) Amorphous polyester graft polymer alloys
CA1168790A (en) Flame-retardant molding composition including a specific copolymer, polyvinyl chloride and a specific graft copolymer
KR960014264A (en) Light diffuser composition
CA1093808A (en) Lubricant composition for vinyl chloride polymers
BR9206960A (en) Composition composition suppressant additive substrate material and molded product or article
US3634280A (en) Glowing bouncing putty
JPS575755A (en) Dunkelsperser
US3897389A (en) Flame retardant compositions
US4236715A (en) Amusement device of coated paper and adherable object of oil-extended radial teleblock copolymer
US3261793A (en) Vinylidene polymer films with mixtures of mgo and epoxidized soybean oil
KR830004347A (en) Vinylidene Chloride Copolymer Latex Composition
KR860001417A (en) Magnetic recording media
US2273262A (en) Stabilized vinylidene chloride compositions
ES480960A1 (en) Plasticized PVC compositions.
US2782176A (en) Halogen containing vinylidene resins stabilized with a mixture of zinc and calcium salts of phenyl carboxylic acids
JPH0412724B2 (en)
DE68922824D1 (en) Stable mixtures with low loss of styrene from unsaturated polyesters and vinyl esters.
US2317137A (en) Polystyrene plastic
JPS6176547A (en) Molded products for light diffusion and transmission
EP0604843A3 (en) Transparent and impact-resistant moulding compounds.
GB1008994A (en) Flame retardant composition
KR890701682A (en) Vinylidene chloride interpolymer
GB2042578A (en) Phosphorescent plastics compositions