GB2038478A - Thermochromic Composition - Google Patents
Thermochromic Composition Download PDFInfo
- Publication number
- GB2038478A GB2038478A GB7943636A GB7943636A GB2038478A GB 2038478 A GB2038478 A GB 2038478A GB 7943636 A GB7943636 A GB 7943636A GB 7943636 A GB7943636 A GB 7943636A GB 2038478 A GB2038478 A GB 2038478A
- Authority
- GB
- United Kingdom
- Prior art keywords
- article according
- temperature
- article
- organic material
- decomposable
- 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.)
- Granted
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K9/00—Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
- C09K9/02—Organic tenebrescent materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C61/00—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
- B29C61/06—Making preforms having internal stresses, e.g. plastic memory
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C61/00—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
- B29C61/06—Making preforms having internal stresses, e.g. plastic memory
- B29C61/0608—Making preforms having internal stresses, e.g. plastic memory characterised by the configuration or structure of the preforms
- B29C61/0666—Making preforms having internal stresses, e.g. plastic memory characterised by the configuration or structure of the preforms comprising means indicating that the shrinking temperature is reached
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C67/00—Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
- B29C67/0007—Manufacturing coloured articles not otherwise provided for, e.g. by colour change
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01K—MEASURING TEMPERATURE; MEASURING QUANTITY OF HEAT; THERMALLY-SENSITIVE ELEMENTS NOT OTHERWISE PROVIDED FOR
- G01K11/00—Measuring temperature based upon physical or chemical changes not covered by groups G01K3/00, G01K5/00, G01K7/00 or G01K9/00
- G01K11/12—Measuring temperature based upon physical or chemical changes not covered by groups G01K3/00, G01K5/00, G01K7/00 or G01K9/00 using changes in colour, translucency or reflectance
- G01K11/16—Measuring temperature based upon physical or chemical changes not covered by groups G01K3/00, G01K5/00, G01K7/00 or G01K9/00 using changes in colour, translucency or reflectance of organic materials
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
Heat-recoverable articles carrying a "thermochromic" composition comprising organic materials which melt and decompose to provide a colour-change indicating that the articles have been heated to a certain temperature, e.g. to melt a sealant carried on the surface of the article which is to contact a substrate around which the article is to be shrunk. Mixtures of relatively simple compounds may be used to graduate the colour change, and means are described for preventing reversion to the original colour on long-term exposure to moisture.
Description
SPECIFICATION
Thermochromic Composition
This invention relates to thermochromic compositions and more especially to such compositions in the form of coating compositions, such as paints, and markers such as crayons.
Thermochrnmic materials are those which change colour on being heated to a typical, usually well-defined, temperature. The change in colour is frequently reversible and associated with a reversible chemical change which occurs at that temperature. Such materials are discussed and reviewed, for example, in two articles by Jess. He. Day in Chem. Rev. 63, 65 (1963) and Chem. Rev.
68,649(1968).
Typically thermochromic materials are used as warning indicators that a certain maximum safety temperature has been reached or as means whereby a subsequent check will reveal that some critical temperature was attained; they have also found use in desk thermometers where different materials indicate different temperatures.
One especially interesting application of thermochromic materials has been in the field of heatrecoverable articles such as the heat-shrinkable polymeric sleeves described and claimed in U.S.
Patents Nos. 2,027,962; 3,086,242 and 3,957,372 and the heat-shrinkable wraparound sleeves described and claimed in U.S. Patent No. 3,379,218 and British Patents Nos. 1,155,470: 1,211,988 and 1 346,479. Another type of heat-recoverable article is described in British Patent No. 1 440,524 in which an elastomer member such as an outer tubular member is "held out" in a stretched state by a second member, such as an inner tubular member, which upon heating weakens and thus allows the elastomeric member to recover.
These heat-recoverable articles are typically provided with a sealant coating, for example on the inner surface of a heat-shrinkable sleeve, so that a seal is made between the sleeve and a substrate such as a pipe or cable when the sleeve shrinks around it. The sealants are usually mastics or hot-melt adhesives, for example those described and claimed in British Patent No. 1 ,440,8 10 and German OS 2,723,1 16. In such cases, heat is required both to shrink the expanded plastics material and to melt the sealant. The heating means is often simply a torch which may degrade the plastic if it becomes too hot and yet, on the other hand, it is important that sufficient heat is applied to cause the sealant to melt and flow when in contact with the substrate. it has been proposed therefore in, for example, U.S.
Patent No. 3,816,335 and British Patent No. 1,511,053, to use a suitable thermochromic paint on the surface of the heat-recoverable article in order to monitor and control the heat during recovery.
The use of these materials has been successful but those so far proposed have been inorganic in nature, which may occasionally be environmentally undesirable, and they have in general also exhibited a reversible colour change. This has caused some problems in applications where a check is made some time after recovery to ensure that the heat-recoverable device was heated to the correct temperature. A further problem has been that the basic (i.e. low temperature) colour of the inorganic thermochromic substance has clashed with design and/or coding requirements.
The present invention provides a heat-recoverable article which is to be heated to a pre-selected temperature during installation or use, which carries a temperature indicating composition comprising an organic material which on heating of the article to the said temperature melts and decomposes to provide a visible colour change. We have found that temperature-indicating compositions which are satisfactory for use on heat-recoverable materials can be based, according to the present invention, on surprisingly simple and inexpensive organic materials which decompose at or about their melting point.
As will be explained in more detail hereinafter the materials are, in some respects, not classically "thermochromic" insofar as the colour change is generally irreversible. However, for convenience, they will hereinafter be referred to as thermochromic materials.
The essence of the present invention is that the thermochromic ingredient melts and decomposes on heating to a certain temperature (or narrow temperature range) and yields a decomposition product which has a different colour. In addition, on melting, a change in refractive index usually occurs which
usefully acts as an indication of the onset of the irreversible colour change.
One advantage of using such materials is that they may themselves be virtually colourless thus
allowing the use of conventional pigments for colouration and, for example, of fluorescent and/or
phosphorescent substances for specific design purposes.
The substances preferably decompose at a temperature which is not more than +100C, preferably
not more than +5 C different from the melting point. Given this concept, those skilled in the art will
readily be able to choose suitable low-cost, non-toxic and, often, naturally-occurring materials for any given temperature. However, for heat-recoverable articles the temperature range of interest is typically from about 600C to 4000 C, advantageously from 1 800C to 3000 C, and the materials listed in the following Table have been found to be especially useful, the relevant decomposition temperature being
indicated.Those compounds marked with a cross are thought to be most advantageous and, in
particular, allantoin (white to black), absorbic acid (white to black), lactose (white to black), creatine
(white to black) and azo dicarbonamide (yellow to black) have been found most useful at their
respective temperatures. Others which are found likely to be advantageous for particular end uses are
D(+)-galactose, sucrose, methylene blue, #-aIanine, methyl violet, glycine, nicotinic acid-N-oxide and 5-aminosalicylic acid.
It will be appreciated that may variations and modifications are possible within the basic concept of the present invention. For example the thermochromic ingredient may be part of an aqueous or nonaqueous vehicle comprising, for example, a polymeric binder, or may be part of a solid formulation, for example, a crayon based on a wax such as a paraffin wax. The nature of the thermochromic formulation will, of course, depend on the end use in a specific application.
Table
Tm
Preferred (decomposition)
1,2-Benzoquinone 60--70 Citraconic acid X 93
Azobisisobutyronitrile 102-- 103 C
Fructose X 103-1050C Methyl yellow X 111
2,3-benzoxazin-1 -one 120
Formamidine sulfinic acid 124-127 D(+) Maltose X 130
Malonic acid 132 1 3-acetonedicarboxylic acid X 133
4-aminosalicylic acid 135 5-anilino-1 ,2,3,4-thiatriazole X 146 1-phenyl-5-mercapto-tetrazole 150
Formamidine acetate X 165
D(+)-galactose X 170 d(-)-tartaric acid X 171-174 Aminoguanidine bicarbonate X 170
Oxytetracycline 182-184 Chinolinic acid X 185
Sucrose X 190~192 Ascorbic acid X 190~194 Methylene blue X 190 2-hydroxy-1 ,4-dinaftoguinone X 192-195 2-methyl-3-indolylacetic acid 196-197 Guanidinecarbonate X 198
P-aminophenylacetic acid 1 99-200 5-amino-tetrazole monohydrate 200~204 ss-alanine X 200
L-glutamic acid X 205
Methyl violet X 208~210 L-lysine 210
2,4-dihydroxybenzoic acid 214-216 4-hydrazinobenzoic acid 215
Azodicarbonamide X 215
a-lactose X 219 3-amino-1 -phenyl-pyrazolone 220
4-amino-3-hydroxy-butyric acid 225 4-amino-3-hydrazino-5-mercapto-1 ,2,4-triazole 228~230 Allantoin X 234
Imino-diacetic acid 240
Dimethylglyoxime 242
Oxalic acid dihydrazide 242-244 Ethylene diamino tetra acetic acid X 245
Glycine X 250
Hesperidin 250~255 Barbituric acid 250~252 Nicotinic acid-N-oxide 260
Phenyl-2-piperidyl-acetic acid 260~265 Succinamide 263-266 DL-phenylalanine X 271-273 5-amino-salicylic acid 280
DL-methionine X 281
DL-alanine X 290
Table (contd.)
Tm
Preferred (decomposition)
N-hydroxyethyl ethylenediamine triacetic acid
trisodium salt dihydrate 288~290 Creatine X 295
2-amino octanic acid 295
Maleic acid dihydrazide X- 300
Nile blue X 305
2-hydroxy-benzimidazole 318 1 ,4-benzenedicarboxylic acid X 325
Dinicotinic acid X 325
4,4-azobenzenedicarboxylic acid X 330
6-uracilcarboxylic acid X 347
Melamine X 354
Guanine X 360
Oxamide X 400
However, as will be understood from the foregoing discussion, the present invention is especially useful in the thermochromic marking of heat-recoverable articles, especially heat-shrinkable tubing, wrap-around sleeves and end-caps. For this purpose, it is advantageous to formulate a coating composition usually comprising a polymeric binder.
For example, one currently preferred thermochromic paint for the production of heat-recoverable articles according to the invention comprises the organic thermochromic material, e.g. allantoin, a polymeric binder, e.g. an acrylic resin, and an organic solvent, preferably a halogenated, e.g.
chlorlnated, solvent. Chlorinated solvents have been especially useful because they are good solvents for the binder, have low toxicity, are non-flammable and evaporate quickly at room temperature because of their high vapour pressures. Amongst suitable chlorinated solvents there may be mentioned 1,1,1 -trichloroethylene and mixtures thereof. Suitable binder resins include acrylic resins such as
Paraloid B-66 (Rohm a Haas) which is a copolymer of n-butylmethacrylate with methylmethacrylate.
Other suitable materials include ethylene/vinyl acetate copolymers, ethylene/alkylacrylate copolymers, chlorinated polyethylenes, vinyl chloride homo- and co-polymers, especially vinylacetate/vinyl chloride co-polymers which may be wholly or partially hydrolyzed, and polyvinyl acetate, which may also be partially hydrolyzed.
However, it must be emphasized that other materials will be suited to different applications, including, for example, water-based latex paints.
Equally, the amount of thermochromic material incorporated may vary according to the application but in the coating compositions described above, will typically be in the range of from 1 to 20%, especially from 5 to 10%, based on the weight of the composition.
Other ingredients can be added as appropriate. For example a pigment such as an organic dye, e.g. sunfast blue or sumatra yellow may be added for colouring purposes. Thickening agents, e.g.
fumed silica (e.g. Cab-O-Sil and Aerosol) may be added to improve the rheological properties. In this respect, organic thickening agents which low melting points are especially preferred because they do not interfere with the colour change.
One such organic thickening agent is Thixatrol ST which is a derivative of castor oil sold by
National Lead which may be used at levels of 0.5% by weight and higher, especially 1% and more, in the above described formulations.
Antioxidants, such as Irganox 1010 and Platinox 1212, and plasticizers such as dioctyl phthalate may also advantageously be incorporated.
It is usually preferred to use a temperature-indicating composition according to the present invention which is initially green in colour, and this may be achieved by addition of suitable dye-stuffs to the formulation. A colour change to black or near-black is often desirable for optimum appearance when black heat-recoverable articles are installed, and this is readily achieved by the use of the aforementioned materials which decompose at the relevant temperature to give black or near-black decomposition products.
Mixtures of the decomposable materials may be used to produce a more gradual colour change as a signal to the operator that the desired temperature is being approached, and in such cases it is preferred to use about 9 parts of a material having a higher decomposition temperature to one part of material(s) having a lower decomposition temperature. For example nine parts of allantoin to one part of ascorbic acid or sucrose could be used.
In some cases it has been found that the decomposition products may be leached out by long term exposure to moisture leaving behind a shell of binder which may incorporate enough dyestuff to resemble the original (unheated) colour of the chromogenic paint, thus leading to confusion as to whether or not the heat-recoverable product was correctly heated on installation. This effect can be rendered less troublesome by including in the formulation a background-colouring dyestuff which is itself decomposed during the heating. Methylene Blue is one possible material for this purpose but it is preferred to use the less water-soluble dyestuff Indigo Blue. A most preferred approach, however, is to attach the dyestuff or pigment to the decomposable material (e.g. allantoin) preferably by chemical coupling and preferably before it is incorporated in the temperature indicating composition.The coupling bond may be ionic or covalent, and suitable bonds may be obtained by the use of appropriate coupling agents, for example sulphonyl or cyanuric chloride.
The thermochromic composition of the present invention is especially useful on heat-recoverable articles which are to be applied around a body, e.g. a cable splice, and have on their interior surface installed a coating which must be melted to ensure adequate sealing of the resulting enclosure. The composition in such cases is formulated to produce the colour change when the exterior surface of the article has been heated to a temperature which results in the desired melting of the interior coating when in contact with the substrate (assuming no abnormal heat-sink effects).
The following Example illustrates a typical thermochromic paint formulation for use in accordance with the present invention with heat-recoverable articles.
Parts by
Compound Weight
Paraloid B-66 (Acrylic resin) 4.00
1,1,1 -Trichloroethane 57.69
Perchloroethylene 20.00
Allantoin 16.00
Sunfast Blue or Cinquasia Green 0.06
Irganox 1010 0.25
Plastinox 1212 0.25 # r Dioctyl phthalate 0.50 Methanol/H20 (smoothing agent) 0.25 ", 1 Thixatrol ST 1.00
Whilst one object of the present invention is to provide thermochromic paints and inks which are suitable for use in the monitoring and control of heating plastics articles, especially cross-linked polymeric articles such as the heat-recoverable products mentioned above, it will be appreciated that it is also applicable to other substrates and applications, including, for example, heat-recoverable articles made from memory metals as described in British Patents Nos. 1 327,441 and 1,488,393, especially the preconditioned alloys described and claimed in U.S. Patents Nos. 4,036,669; 4,067,752 and 4,095,999.
In contrast with the previously proposed inorganic thermochromic formulations which have sometimes been adversely affected by heat-aging, or environmentally undesirable, and have had an undesirable tendency to reverse colour, especially under wet or moist conditions and a tendency to deteriorate catalysed by acids and bases with a resultant change in temperature response, the organic compounds of the present invention are generally stable, non-reversible, environmentally acceptable, and give reproducible results.
A further preferred embodiment of the invention is that in which the melting/decomposition temperature is within the range 350#4500 C, most preferably using oxamide (melting point 4000 C) as the decomposable organic material. It has very surprisingly been found that this large increase
(compared with allantoin) iri colour change temperature on the outside of a heat-shrinkable sleeve
results in only about 1 00C increase in the bond-line temperature within the sleeve, and only about 10% increase in sleeve installation time. The oxamide composition may be especially useful in countering
the effects of low-temperature installation environments.
Claims (20)
1. A heat recoverable article which is to be heated to a pre-selected temperature during
installation or use, which carries a temperature indicating composition comprising decomposable
organic material which, on heating of the article to said temperature, melts and decomposes to provide
a visible colour change.
2. An article according to Claim 1, capable of forming an enclosure about a body and carrying on
a surface which will face the interior of the enclosure a meltable composition, wherein the said
temperature indicating composition is carried on a surface which will be visible when the article is
enclosing the body and is formulated to produce said colour change when heated to a temperature
which results in the melting of said meltable composition to effect sealing of the enclosure.
3. An article according to Claim 1 or 2, wherein the decomposition of the organic material in the
temperature indicating composition is substantially irreversible.
4. An article according to any of the preceding Claims, wherein the temperature indicating
composition comprises a mixture of decomposable organic materials which melt and decompose at
different temperatures from one another.
5. An article according to Claim 4, wherein the temperature indicating composition comprises 8.5 to 9.5 parts by weight of a decomposable organic material having a higher decomposition temperature, and 0.5 to 1.5 parts by weight of a decomposable organic material having a lower decomposition temperature.
6. An article according to any of the preceding Claims, wherein the said decomposable organic material is or includes allantoin.
7. An article according to any of the preceding Claims, wherein the said decomposable organic material is or includes ascorbic acid, lactose, creatine, or azo dicarbonamide.
8. An article according to any of the preceding Claims, wherein the said decomposable material is or includes D(+)-galactose, sucrose, methylene blue, #-alanin, methyl violet, lysine, nicotinic acid-Noxide, or 5-amino-salicylic acid.
9. An article according to any of the preceding Claims, wherein the temperature indicating composition is coloured by means of a pigment or dyestuff in addition to the said decomposable organic material.
10. An article according to Claim 9, wherein the said coloured pigment or dyestuff also decomposes during the heating to produce a substantially irreversible visible colour change independently of the colour change brought about by the said decomposable materials.
11. An article according to Claim 9 or 10, wherein the said pigment or dyestuff is attached to the said decomposable organic material.
12. An article according to Claim 11, wherein the said pigment or dyestuff is chemically coupled to the said decomposable organic material.
13. An article according to any of the preceding Claims wherein the said decomposable material is selected to give the said colour change within the range from 350 to 4500C.
14. An article according to Claim 13 wherein the said decomposable material is or includes oxamide.
15. An article according to Claim 1, wherein the temperature indicating composition is substantially as described in the foregoing Example.
16. An article according to any of the preceding Claims, which has been subjected to a temperature such that the temperature indicating composition has undergone said visible colour change.
17. An article according to any of Claims 1 to 16, which has been installed around a suitable shaped body.
1 8. A method of enclosing a body, comprising positioning around the body a heat recoverable article according to any of Claims 1 to 15, and heating the article so as to recover it about the said body and to cause the temperature indicating composition to undergo the said visible colour change.
19. A kit of parts for use in providing a sleeve enclosure around an elongate body, the kit including an article according to any of Claims 1 to 15.
20. A coating composition capable of being applied to an article to form the temperature indicating composition of an article according to any of Claims 1 to 1 5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7943636A GB2038478B (en) | 1978-12-22 | 1979-12-19 | Thermochromic composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7849880 | 1978-12-22 | ||
GB7943636A GB2038478B (en) | 1978-12-22 | 1979-12-19 | Thermochromic composition |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2038478A true GB2038478A (en) | 1980-07-23 |
GB2038478B GB2038478B (en) | 1983-09-28 |
Family
ID=26270080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7943636A Expired GB2038478B (en) | 1978-12-22 | 1979-12-19 | Thermochromic composition |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2038478B (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0042285A1 (en) * | 1980-06-16 | 1981-12-23 | N.V. Raychem S.A. | Thermochromic composition and articles |
WO1984000608A1 (en) * | 1982-07-30 | 1984-02-16 | Raychem Corp | Thermochromic composition |
US4498938A (en) * | 1980-05-12 | 1985-02-12 | N.V. Raychem S.A. | Splicing, branching or terminating cable |
EP0132692A2 (en) * | 1983-07-20 | 1985-02-13 | ANT Nachrichtentechnik GmbH | Heat-recoverable article with temperature indication |
EP0181485A2 (en) * | 1984-10-05 | 1986-05-21 | Röhm Gmbh | Temperature-variable light transmission vitrifications |
US4925727A (en) * | 1982-07-30 | 1990-05-15 | Raychem Corporation | Curable temperature indicating composition |
US5120137A (en) * | 1991-03-29 | 1992-06-09 | Minnesota Mining And Manufacturing Company | Time and temperature indicating device |
DE4140273A1 (en) * | 1991-12-06 | 1993-06-09 | Stewing Gmbh & Co Kg Werk Berlin, 1000 Berlin, De | Useful coatings for heat-shrink prods. - consists of suitable polymer which bonds to heat-shrink article and incorporates indicator to show when correct shrinkage temp. arises |
-
1979
- 1979-12-19 GB GB7943636A patent/GB2038478B/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4498938A (en) * | 1980-05-12 | 1985-02-12 | N.V. Raychem S.A. | Splicing, branching or terminating cable |
EP0042285A1 (en) * | 1980-06-16 | 1981-12-23 | N.V. Raychem S.A. | Thermochromic composition and articles |
WO1984000608A1 (en) * | 1982-07-30 | 1984-02-16 | Raychem Corp | Thermochromic composition |
US4925727A (en) * | 1982-07-30 | 1990-05-15 | Raychem Corporation | Curable temperature indicating composition |
EP0132692A2 (en) * | 1983-07-20 | 1985-02-13 | ANT Nachrichtentechnik GmbH | Heat-recoverable article with temperature indication |
EP0132692A3 (en) * | 1983-07-20 | 1986-06-25 | Ant Nachrichtentechnik Gmbh | Heat-recoverable article with temperature indication |
EP0181485A2 (en) * | 1984-10-05 | 1986-05-21 | Röhm Gmbh | Temperature-variable light transmission vitrifications |
EP0181485A3 (en) * | 1984-10-05 | 1986-09-10 | Rohm Gmbh | Temperature-variable light transmission vitrifications |
US5120137A (en) * | 1991-03-29 | 1992-06-09 | Minnesota Mining And Manufacturing Company | Time and temperature indicating device |
DE4140273A1 (en) * | 1991-12-06 | 1993-06-09 | Stewing Gmbh & Co Kg Werk Berlin, 1000 Berlin, De | Useful coatings for heat-shrink prods. - consists of suitable polymer which bonds to heat-shrink article and incorporates indicator to show when correct shrinkage temp. arises |
Also Published As
Publication number | Publication date |
---|---|
GB2038478B (en) | 1983-09-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PE20 | Patent expired after termination of 20 years |
Effective date: 19991218 |