Disposable reversible thermometer

Claim 2

A composition of matter comprising: (1) a heat-sensitive composition capable of reversibly changing color at a predetermined temperature comprising at least one heat-sensitive phase/color change agent and present in a quantity of from about 40% to about 70% by weight; (2) a non-polar matrix-forming amorphous material present in a quantity of from about 20% to about 40% by weight; and (3) a non-polar film-forming material that is more crystalline than said matrix-forming amorphous material and present in a quantity to form a film over said matrix having said heat-sensitive composition dispersed therein sufficient to prevent subliming of said heat-sensitive composition therethrough, and capable of forming a matrix having said heat-sensitive composition dispersed therein, with the proviso that at least each of (2) and (3) is (a) soluble in said heat-sensitive composition at a temperature of from about 25° C. to about 35° C. above the melting point of said heat-sensitive composition; (b) insoluble in said heat-sensitive composition below the melting point thereof plus at least 5° C.; (c) a non-solvent for any heat-sensitive composition phase/color change agents; (d) inert toward said heat-sensitive composition; and (e) possessed of a melting point at least 15° C. above the melting point of said heat-sensitive composition.

Claim 3

The composition of claim 1 further comprising a solubilizing agent for said heat-sensitive composition and present in a quantity of from about 20% to about 25% by weight, said solubilizing agent being (a) soluble in said heat-sensitive composition at a temperature of from about 25° C. to about 35° C. above the melting point of said heat-sensitive composition; (b) insoluble in said heat-sensitive composition below the melting point thereof plus at least 5° C.; (c) a non-solvent for any heat-sensitive composition phase/color change agents; (d) inert toward said heat-sensitive composition; (e) possessed of a melting point at least 15° C. above the melting point of said heat-sensitive composition; (f) capable of solubilizing said heat-sensitive composition in the balance of the composition at high temperatures in order to make manufacture possible at lower temperatures; (g) insoluble and inert toward said heat-sensitive composition at low temperatures; (h) possessed of a melting point at least 10° C. above the temperature to be measured; (i) inert to said matrix-forming amorphous material and said filmforming material; (j) clear or translucent; and (k) capable of encapsulating materials inert to said solubilizing agent.

Claim 4

The compositions of matter of claim 1, wherein said heat-sensitive composition is substantially free of impurities and consisting essentialy of: (a) a solvent adapted to change from a solid state to aliquid state at substantially a predetermined temperature; and (b) an effective amount of one or more suitable organic moieties dissolved in and inert towards said solvent and adapted to change the color of the composition visible to the naked eye upon the change in state at substantially the predetermined temperature when so dissolved, and selected from one or both of the groups consisting of: (1) one or more of a Group III body of compounds consisting of pinacyanol iodide, 1,1'-diethyl-2,2'-cyanine iodide, quinaldine red, pinacyanol chloride, thionin, methylene blue, cresol red, chlorophenol red, neutral red iodide, neutral red chloride, crystal violet, acridin orange, Orasol Orange RLN™, Orasol Navy Blue™, Irgalith Red PR™, Fat REd BS™, Xylene Cyanol FF™, Rhodamine B™, Rhodamine 6G™, Irgalith Magneta TCB™, Irgalith Pink TYNC™, Toluidine Blue O™, Savinyl Green B™, Savinyl Blue RS™, purpurin, 3,3'-diethylthiadicarboxyanine iodide, cryptocyanine, Dicyanine A™, Merocyanine 540™, 4-(p-ethoxyphenylazo)-m-phenylene diamine monohydrochloride, Yellow Orange S™, Chrysoidan G™, fuchsin, aurintricarboxylic acid (ammonium salt), Victoria Blue R™, Pyronin G™, gallein, Erythrosin Yellow Blend™, chlorophenol blue, bromophenol blue, bromocresol purple, Coriphosphine O™, acriflavine, acridine orange, rhoduline violet, Alizarin cyanin 2R™, Alizarin Red S™,alcannin, Aurantia, Direct Green G™, Fast Red Salt 3GL™, Fast Blue Salt BB™, Fast Garnet Salt GBC™, Carta Yellow G 180 o/o™, Murexide, Savinyl Blue GLS™, Irgalith Blue GLSM™, phthalocyanine, Di Amingreen B™, Alizarin Blue S, Celliton Blue Extra™, neocyanine, Janus Green™, dimethyl yellow, Fast Yellow™, methyl red sodium salt, Alizarin yellow R™, Eriochrome black T™, Chromotrope 2R™, Ponceau 6R™, Brilliant Ponceau G/R/2R, chomolan yellow, Sudan Red B™, Bismarck brown G, Fat Black™, Resorcin Brown™, Benzofast pink 1BL™, Oil Red EGN™, Euroglaucine, Fuchsin NB™, parafuchsin, Patent Blue™, Irgalith Blue TNC™, Phloxin B™, fluorescein sodium salt, Rhodamine B base™, Eosinscarlet, Eosin Yellowish™, Erythrosin extra bluish, 4'5-dibromo fluorescein, ethyleosin, Phloxine™, Cyanovin b™, chlorocresol green, pinacyanol bromide, 2-(p-dimethylaminostyryl)-1-ethyl pyridinium iodide, ethyl red, nigrosine, Savinyl Blue B™, Orasol Blue BLN™, Safranin O™, Azoicarnun G™, Phenosafranine™, Azocarmine BX™, Solophenyl Brilliant Blue BL™, Nile Blue a™, gallocyanine, gallamine blue, celestine blue, methylene green, Azure A/B/C™, Blue VIF Organol™, Alizarin, Nitrofast Green GSB™, quinalizarine, Oil Blue N™, Solvay purple, Ciba Blue™, Indigo synthetic™, Chromophtal Bordeaux RS™, Acid Alizarin Red B™, 5-Aminofluoresecein, Rose Bengal™, Martius Yellow™, Chicago Blue 6B™, Alcian Blue 86X™, cresyl violet, 4,4'Bis (dimethylamino)benzhydrol, Zinc Phthalocyanine, Sudan III™, Pyronin Y™, Toluylene Blue™, cresyl violet perchlorate, Mendola's Blue™, Phosphine Dye™, Nitrol™, cresyl violet acetate, ceres orange R™, 4-phenylazo-1-naphthyl-amine, 4-(4-Dimethylamino-1-naptylazo)-3-methoxybenzene sulfonic acid, Bindschedler's Green™, and p-(p-dimethylaminophenylazo)benzoic acid, or (2) a binary mixture of: (A) one or more of a Group I body of compounds soluble in said solvent consisting of the halogenated sulfonphthaleins and the organic acids having a pK 1 less than about four; and (B) one or more of a Group II body of compounds consisting of the aminotriphenylmethanes and their soluble salts; 8-hydroxyquinoline, and the cyanines; wherein the weight ratio of the Group I body of compounds to the Group II body of compunds is more than or about 3to 1 and with the proviso that if the Group II compounds consist solely of one or more aminotriphenylmethanes or their soluble salts, then the Group I compound must be selected from one or more of the group consisting of oxalic acid, suitable soluble sulfonic acids, and the tetrahalogenated sulfonphthaleins, and the other organic acids having a pK 1 of less than or about 2, and (3) one or more of the aforesaid Group III body of compounds with one or more of the Group I or Group II bodies of compounds.

Claim 5

The composition of matter of claim 3, wherein (a) the Group I body of compounds are one or more of the group consisting of oxalic acid, bromophenyl blue, bromothymol blue, chlorophenol red, bromochlorophenyl blue, bromocresol green, 3,4,5,6-tetrabromophenolsulfonphthalein, 2-naphthalene-sulfonic acid, trichloroacetic acid, chloroanilic acid, bromophenol red, and chlorocresol green, and (b) the Group II body of compounds are one or more of the group consisting of ethyl red, crystal violet, pararosaniline, pararosaniline acetate, 3-ethyl-2-[5-(3-ethyl-2-benzothiazolinylidene)-1,3-pentadienyl]-benzothiazolium iodide, basic fuchsin, 8-hydroxyquinoline, ethyl violet, brilliant green, dicyanine, pinacyanol chloride, 1-ethyl-pyridinium iodide, 3,3'-diethylthiodicarbocyanine iodide, and cryptocyanine.

Claim 6

The composition of matter of claim 4, wherein the weight percentage of organic moieties soluble in the solvent is from about 0.025 to about 0.05% of the weight of the solvent and said soluble organic moieites.

Claim 7

The composition of matter of claim 4, wherein the predetermined temperature is from about 96° F. to about 105° F.

Claim 8

The composition of matter of claim 4, wherein the solvent is selected from one or more of the group consisting of ortho-chloronitrobenzene, ortho-bromonitrobenzene, 1-thymol, 2-naphthol, 2-ethoxybenzamide, and naphthalene.

Claim 9

The composition of matter of claim 4, wherein the solvent is a binary mixture of ortho-chloronitrobenzene and ortho-bromonitrobenzene having a proportion of orthochloronitrobenzene to ortho-bromonitrobenzene of about 43.8:56.2 to about 4.0:96.0.

Claim 10

The composition of matter of claim 4, wherein the Group I compounds consist of the halogenated sulfonphthaleins having a pK 1 of about 2 and a pK 2 of about 7 to about 9.

Claim 11

The composition of matter of claim 1, wherein said matrix-forming amorphous material is polyisobutylene.

Claim 12

The composition of matter of claim 1, wherein said film-forming material is selected from the group consisting of paraffin wax, and low molecular weight polyethylene.

Claim 13

The composition of matter of claim 2, wherein said solubilizing compound has the formula C n H 2n-1 OH, wherein n is in the range of 18 to 24.

Claim 14

The composition of matter of claim 2, wherein said solubilizing compound is docosanol.

Claim 15

The composition of matter of claim 1, wherein said heat-sensitive composition consists essentialy of pinacyanol iodide and a mixture of ortho-chloronitrobenzene and orthobromonitrobenzene.

Claim 16

A composition of matter comprising: (a) a heat-sensitive composition capable of reversibly changing color at a predetermined temperature substantially free of impurities consisting essentially of an effective amount of pinacyanol iodide in a solvent consisting of a mixture of orthochloronitrobenzene and ortho-bromonitrobenzene; (b) polyisobutylene; (c) HISTOWAX® HX482; and (d) docosanol; the weight ratio of (a):(b):(c):(d) being approximately 48:26:5:21.

Claim 17

A composition of matter comprising: (a) a heat-sensitive composition capable of reversibly changing color at a predetermined temperature substantially free of impurities consisting essentially of an effective amount of pinacyanol iodide in a solvent consisting of a mixture of orthochloronitrobenzene and ortho-bromonitrobenzene; (b) polyisobutylene; (c) HISTOWAX® HX482; and (d) docosanol; the weight ratio of (a):(b):(c):(d) being approximately 48:26:5:21.