This invention relates to an apparatus for indicating the passage of time to a viewer, a method therefor, and an article or container therewith such as badges and containers that are used in connection with a time-sensitive product or a service.
Many products or services presently available to a consumer are “time-sensitive” in the sense that their freshness, efficacy and/or safety have a limited time duration, or “shelf life”. There have been various attempts to provide a time-indicating apparatus that enables a consumer to track the time before which a product becomes unusable.
A time-indicating apparatus relies upon the change in color of a substance from an initial perceived color to a final perceived color. The time interval during which the change from the initial to the final perceived color of the substance occurs is termed the “color transition time interval”. In the context of this application this interval is measured from the time that the substance begins to transition away from the hue of the initial perceived color and ends when the final hue is achieved. A preliminary “delay time interval” may be defined from some initial time milestone until the onset of the color transition time interval. The overall “elapsed time” for the operation of the time-indicating apparatus is the sum of the delay time interval and the color transition time interval.
Time-indicating apparatus can be based on dye diffusion or on reaction of a reduced dye with oxygen where the reaction is carried out within an enclosed receptacle. See, e.g., U.S. Pat. Nos. 4,903,254, 5,633,835, and 3,480,402 and WO 02/46741.
To manufacture the time-indicating apparatus based on the reaction of a reduced dye with oxygen the dye is reduced outside of the receptacle and then deposited onto a filter paper substrate. The substrate is rinsed before it is inserted into the receptacle. This process is time-consuming and raises the process cost for producing the apparatus. Further, due to the uncontrolled absorption of the dye and the reducing agent on the filter paper it is difficult to control precisely the amount of reduced dye and excess reducing agent packaged within the receptacle. This makes it difficult to control the length of the color transition time interval and the elapsed time.
Time-indicating technology based on reaction of oxygen with a reduced redox dye can also deal with monitoring time-temperature history for packaging where a predetermined time-temperature combination is determined from the concentration of zinc in solution. See, e.g., U.S. Pat. No. 3,768,976 which includes a lamination step and dye reduction is performed outside the pouch. These steps, among others, make it likely that the cost to manufacture such a system is high. In addition, the time-indicating method uses a considerable amount of liquid that contains reactive ingredients and breakage of the pouch may create a safety hazard.
Accordingly, in view of the foregoing it is desirable to provide an apparatus for indicating the passage of time and to a method for making that apparatus that is economical. It is also believed to be advantageous to provide a time-indicating apparatus in which both the delay time and the color transition time are able to be precisely adjusted. It is believed to be of further advantage to provide an article that includes a time-indicating apparatus such as a container or a badge useful with a time-sensitive product or service.
Such time-indicating apparatus and methods of making and using the same are believed to provide significant cost and performance advantages to a user over those available in the prior art.
The present invention is directed to a time-indicating apparatus and to methods of making and using the same. The time-indicating apparatus in accordance with the present invention is based on the color change property of a reduced redox dye in the presence of oxygen.
The present invention is characterized by the initial introduction into a receptacle of a predetermined metered amount of a redox dye in its oxidized form together with a predetermined effective amount of a reducing agent in an alkaline medium. The receptacle is then sealed. The conversion of the oxidized form of the redox dye into its reduced form occurs in situ (i.e., within the receptacle). The receptacle is made of one or more materials such that oxygen is able to enter into the interior volume of the receptacle at an oxygen transmission rate in the range from 0.1 cc-mil/100 inch2-day-atm to 350 cc-mil/100 inch2-day-atm.
Precisely controlling the amount of both the oxidized dye and the amount of reducing agent that are introduced into the receptacle ensures that only a predetermined amount of the reduced form of the redox dye is able to be formed within the receptacle. By controlling the amount of reduced dye able to be formed within the receptacle and by controlling the rate at which oxygen is able to enter into the receptacle (by the selection of the materials used to fabricate the receptacle and the surface area of the receptacle) the color transition time interval of the redox dye is able to be precisely controllable.
The amount of reducing agent introduced into the receptacle may be exactly that amount needed to convert the entire amount of the oxidized form of redox dye into its reduced form. Alternatively, either an amount in excess of, or an amount less than, this amount of reducing agent may be introduced into the receptacle. A reducing agent is an aqueous solution comprising sodium hydrosulfite (“hydro”) and sodium hydroxide (NaOH). A moisture retainer, such as glycerol, may also be included in the solution.
An oxygen-scavenging material able to react more quickly with oxygen than does the redox dye may also be introduced into the receptacle. The amount of oxygen-scavenging material within the receptacle is determined in accordance with the oxygen transmission rate into the receptacle and the surface area of the receptacle such that a predetermined delay time is defined prior to the onset of the color transition time. The duration of the delay time is adjustably selectable in accordance with the amount of oxygen-scavenging material.
Since a reducing agent is itself an oxygen-scavenging material, when an excess amount of this reducing agent is used, that portion in addition to that required to convert the oxidized dye to the reduced form serves to control the delay time. In the other instances when the exact amount or a lesser amount of a reducing agent is used (or, if a reducing agent that is not able to serve as an oxygen scavenger is used) an additional oxygen-scavenging material could be disposed in the receptacle.
It is contemplated that immediately after manufacture, the time-indicating apparatus of the present invention will typically be enclosed in a jacket formed of a suitable oxygen-impermeable material. Upon rupture of the jacket, diffusion of oxygen into the receptacle may begin. The time-indicating apparatus of the present invention may be used with a wide variety of containers within which a myriad of time-sensitive products may be packaged. The time-indicating apparatus may also be used in connection with a service, such as in a badge (e.g., a security pass for indicating the expiration of a period of legitimacy) or for indicating a time for lubricant or filter replacement. In any case the time-indicating apparatus may be attached on the exterior or disposed within the interior of the container or badge, as the case may be. Of course, if the time-indicating apparatus is sealed within the interior of the container or badge, an oxygen-impermeable jacket is likely not used.
The invention will be more fully understood from the following detailed description thereof, taken in connection with the accompanying drawings, which form a part of this application and in which:
Throughout the following detailed description similar reference characters refer to similar elements in all Figures of the drawings.
As summarized above, in one aspect the present invention is directed to a time-indicating apparatus that utilizes a transition of a reduced redox dye to a final perceived color of an oxidized dye as the signal to a user that a predetermined time period has elapsed. The overall elapsed time period (ET) is graphically indicated in
The time interval during which the reduced redox dye changes from its initial perceived color coto its final perceived color c2 is termed the “color transition time interval” denoted in
A preliminary “delay time interval” (DT) is defined as extending between the initial time milestone to and time t1(which indicates the onset of the color transition time interval CTT). At some point during the delay time interval the reduced redox dye achieves its initial perceived color c0. There may be instances in which the redox dye undergoes preliminary color modifications before the initial perceived color is achieved. These color modifications are not indicative of the onset of the color transition time interval, but are merely prefatory changes necessary for the reduced redox dye to achieve a condition wherein the initial perceived color may be exhibited.
As the hues of the reduced redox dye progress from the initial perceived color c0 toward the final perceived color c2 they pass through a “contrast color range” c0. The beginning of the contrast color range c1 occurs at a time tm, where tm is between the times t1 and time t2.
As will be fully developed herein the time-indicating apparatus of the present invention may also include a message indicia disposed therein. The message indicia is rendered in a predetermined message color. The message color can be selected such that it is obscured by hues outside of the contrast color range c1, but exhibits a discernible contrast with the hues within the contrast color range c1. The interval between times tm and the time t2 thus defines a “message appearance time interval” (MAT) during which the message indicia exhibits increasingly higher contrast to the hues in the contrast color range, thus becoming progressively more and more visible to a viewer.
With reference to
The receptacle 12 may be configured in any of a variety of forms. Preferably, as shown in
Barrier Film
Any of a number of various polymeric materials may be used for the barrier films 16, 18. The polymeric materials are desirably inert to the contents of the receptacle 12. Suitable polymeric materials include polyamide, polyester, polyvinyl chloride, polyvinylidene chloride, polyethylene, and polypropylene (unoriented or biaxially oriented). Heat-sealable polyester films and nanoclay-containing films are also suitable. Coated materials such as poly(vinylidene chloride)-coated polyethylene terephthalate (PET) film or poly(vinylidene chloride)-coated polypropylene film may also be used to decrease the rate of oxygen transmission into the interior volume of the receptacle. Other suitable coatings include silica, carbon, aluminum, polyvinylidene chloride (PVDC), or polymers containing nanoclay particles.
Any combination of polymeric materials may be selected for use as the barrier films 16, 18 such that oxygen is able to enter into the interior volume 14 of the receptacle 12 at an oxygen transmission rate in the range from range from 0.1 cc-mil/100 inch2-day-atm to 350 cc-mil/100 inch2-day-atm. The amount of oxygen entering the receptacle 12 is also affected by the thickness of the barrier films 16, 18 and the total surface area of the receptacle. Preferably, each of the barrier films 16, 18 has a thickness dimension in the range one-half mil (0.5 mil) to five mils (5 mils) (12 μm to 125 μm).
The mode of forming the peripheral seals 20 can also assist in controlling the rate of oxygen transmission. For example, the peripheral seal can be formed using a heat seal, an adhesive or a mechanical clamp or fastener.
In the embodiment of the invention illustrated in
Redox Dye
Any redox dye or mixture of redox dyes, including leucomethylene blue, indigo carmine, Ciba Scarlet B. G., Cibanone Yellow, sodium anthraquinone beta-sulfonate, may be used. The weight of the reduced redox dye disposed in the receptacle having a surface area of approximately four square inches (4 in2; 6.45 cm2) is preferably in the range from 0.025 mg to 200 mg, and more preferably in the range from 0.025 mg to 1 mg.
A preferred redox dye is a Cibanone Yellow dye. The reduced form of this dye gives a perceived initial color as intense blue or red-orange (depending upon the ratio of the components of the preferred reducing agent, to be discussed). The perceived final color of the oxidized form of this dye is yellow.
Interestingly, it has been found that when relatively low barrier films, like polypropylene, are used to form the receptacle, the color change starts at the edge of the dyed area of the substrate 24 and proceeds toward the center.
Substrate As illustrated in
In another embodiment it lies within the contemplation of the present invention that the reduced redox dye 22 may be directly received within the interior volume 14. For example, the reduced redox dye 22 may be disposed in the form of a powder, a pill, a liquid, or a gel. In those instances, a separate message panel (not shown) may be placed in the receptacle 12 and positioned beneath the reduced redox dye.
In accordance with the present invention the redox dye is introduced into the receptacle 14 while in its oxidized form. The redox dye is converted in situ (i.e., within the interior volume 14 of the receptacle 12) in the presence of a predetermined metered amount of a reducing agent in an alkaline medium that is also introduced into the receptacle 12 prior to the sealing thereof. The reducing agent in an alkaline medium is illustrated diagrammatically in
At some point the receptacle also has a predetermined amount of spent reducing agent therein. For purposes of illustration the spent reducing agent 28 is diagrammatically indicated in
Reducing Agent
Suitable reducing agents include ammonium sulfate, ferrous compounds, sodium hydrosulfite (“hydro”), monosaccharides, and oligo-saccharides, ascorbic acid, or glucose. The preferred reducing agent is an aqueous solution of sodium hydrosulfite (“hydro”) and sodium hydroxide (NaOH).
The reducing agent can be introduced in an alkaline medium, which can be made from deoxygenated water containing metered alkali.
The ratio of the sodium hydrosulfite (“hydro”) to sodium hydroxide (NaOH) determines the initial perceived color of the redox dye. The ratio of sodium hydrosulfite to sodium hydroxide can be in the range from one (1) to eight (8), or from one (1) to four (4).
The ratio of the reducing agent in an alkaline medium to the redox dye is in the range from sixteen to ten thousand (16 to 10,000).
Color Transition Time Interval Control
A feature of the time-indicating apparatus 10 of the present invention is the ability to control precisely the duration of the color transition time interval. In accordance with the present invention this control is achieved by disposing within the receptacle 12 a predetermined amount of the reduced form of redox dye. The desired amount of the reduced form of redox dye is determined in accordance with the oxygen transmission rate into the receptacle and the surface area of the receptacle. Both of these factors influence the amount of oxygen entering the receptacle. Control over the precise amount of reduced redox dye is achieved by initially introducing an oxidized form of the redox dye into the receptacle and thereafter introducing a predetermined effective amount of a reducing agent into the receptacle. The precise predetermined amount of the reduced redox dye is thereby produced in situ (i.e., within the receptacle) by the conversion of the oxidized form.
In one case, the effective amount of the reducing agent introduced into the receptacle substantially equals only that amount necessary to convert all of the oxidized form of the redox dye into its reduced form.
However, as an alternative, the effective amount of the reducing agent may be in excess of that necessary to convert all of the oxidized form of the redox dye into its reduced form, thus leaving an excess of reducing agent within the receptacle.
As a further alternative, the effective amount of the reducing agent may be less than that amount necessary to convert all of the oxidized form of the redox dye into its reduced form. In this instance a remainder portion of the oxidized form of the redox dye remains in the receptacle. (The presence of an excess of reducing agent or a remainder portion of the oxidized dye within the receptacle is an embodiment of “other receptacle contents” 29 and is diagrammatically indicated in
Delay Time Interval Control
An oxygen-scavenging material able to react more quickly with oxygen than does the reduced redox dye may also be introduced into the receptacle. The amount of oxygen-scavenging material within the receptacle is determined in accordance with the oxygen transmission rate into the receptacle and the surface area of the receptacle. The duration of the delay time interval DT (
Since the preferred reducing agent is itself an oxygen-scavenging material, when an excess amount of this reducing agent is used, that portion in addition to that required to convert the oxidized dye to the reduced form serves to control the delay time. In the other instances when the exact amount or a lesser amount of the preferred reducing agent is used (or if a reducing agent that is not able to serve as an oxygen scavenger is used) an additional oxygen-scavenging material could be disposed in the receptacle.
Oxygen-Scavenging Material
Any oxygen-scavenging material, preferably one that is activated by ultraviolet light, may be used. Suitable oxygen-scavenging materials include the oxygen-indicating tablets sold by Mitsubishi Chemical Company under the trademark, “Ageless®”, such as Ageless® E-200 oxygen-indicating tablets. The ultraviolet light activatable polymeric oxygen-scavenging system sold by Cryovac Company as Cryovac® OS2000 system, or the ultraviolet light activatable semiconductor formulation described in PCT published application WO 2004/005424, may also be used. Other suitable oxygen-scavenging materials include tannin, carbohydrazide and the material sold by Completion Products and Services as OS-8, an organic salt that is a non-sulfur-based oxygen scavenger. An ultraviolet light activatable material may be preferred as it offers the advantage for longer shelf life for a time-indicating apparatus because it removes the necessity of storage of the time-indicating apparatus in a non-oxygen environment.
Moisture Retainer
The receptacle may also contain a moisture-retaining material. Suitable moisture-retaining materials include glycerol, water-glycerol mixture, PEG, agar-water mixture. (The presence of the moisture-retaining material in the receptacle is another embodiment of “other receptacle contents” indicated by 29 in
Combinations of excess reducing agent/remainder portion of the oxidized dye, oxygen scavenging material and/or moisture retainer may be included in “other receptacle contents” indicated by 29 in
Oxygen-Impermeable Jacket
The receptacle 12 can be enclosed in a oxygen-impermeable jacket 30 formed from superimposed upper and lower sheaths 32, 34, respectively. The sheaths are sealed in an oxygen-impermeable manner along their mutually abutting edges, as suggested by reference character 36. Portions of the upper sheath 32 of the oxygen-impermeable jacket 30 and one of the films 16 forming the receptacle are broken-away in
A region of the upper sheath 32 is perforated, as at 38, to define a removable tab 40. With the tab 40 in place, no oxygen is available for transmission into the receptacle 12. However, removal of the tab 40 exposes a portion of the upper film 16 to oxygen, thereby permitting oxygen transmission into the receptacle 12. This action denotes the time to and starts the delay time interval.
Alternatively, instead of using an oxygen-impermeable jacket the reducing agent may be encapsulated in a film or in a frangible material, such as crosslinkable polyethers, vinyl terminated polydimethylsiloxane, alginate, etc.
The message indicia 42 may be carried on the paper substrate 24, in which event it may be printed in a water insoluble ink. Alternatively, the indicia may be printed or otherwise attached to the film 16 or 18 or to a separate message panel disposed within the receptacle.
The indicia 42 is rendered in a color that is obscured by hues outside of the contrast color range c1 (including the initial perceived color c0) but has a discernible contrast with hues within the contrast color range c1 and including the final perceived color c2. As such, the indicia becomes more visible as the redox dye changes from the initial perceived color c1 to the final perceived color c2.
As seen in
More than one message indicia may be used in a time-indicating apparatus 10. Each message indicia is rendered in a predetermined color that is either obscured or discernible to a viewer based upon the color contrast range and message appearance time.
With reference to
The product or article can be any item whose freshness, efficacy and/or safety has a limited time duration or an inherent, optimum, lifetime. An illustrative (but not exhaustive) list of such products would include: processed foods (e.g., baby food,
The container is constructed in any convenient manner and may exhibit any convenient size and shape to accommodate any of the listed articles.
An apparatus 10 for indicating the passage of time in accordance with the present invention is attached to the container. As used throughout this description and claims, by “attached” it is meant that the apparatus 10 is positioned in any convenient location on or within the container such that the redox dye within the receptacle 12 is presented to and is visible by a viewer.
The time-indicating apparatus 10 may be attached to either the exterior of the container (
A supply strip 102 of substrates 24 is conveyed on a supply conveyor 104 in a direction 106 toward a loading station 108. The loading station 108 is located adjacent to a main processing conveyor 110. Each of the substrates 24 contains a predetermined metered amount of an oxidized form of a redox dye 22 deposited thereon. A message indicia 42 is printed on the substrate 24. The deposit of the oxidized redox dye 22 and the printing of the message indicia 42 may occur in a preliminary manufacturing line adjacent to the supply conveyor 104 or elsewhere.
The main processing conveyor 110 moves in a direction 112 past the loading station 108. A strip of metallic foil forming the lower foil sheath 34 of the oxygen-impermeable jacket and the lower polymeric film 18 are carried, one atop the other, by the main processing conveyor 110.
At the substrate loading station 108 individual paper substrates 24 are cut from the supply strip 102 by a cutter 114 and sequentially deposited onto the lower polymeric film 18 on the main processing conveyor 110. This action is diagrammatically indicated by the reference arrow 116. The paper substrates 24 are laid on the film 18 with a predetermined spacing distance 118 defined therebetween.
The substrates 24 are conveyed into a housing 122 containing a non-oxygen atmosphere. Although any inert atmosphere may be used, a nitrogen atmosphere is preferred. At a dispensing station 124 within the housing 122 a predetermined metered amount of a reducing agent is deposited onto each substrate 24. It is important that the reducing agent is carried in an alkaline medium. It has been found that adding hydro alone to either a dyed substrate or a dyed substrate containing an alkaline compound does not result in full conversion of the redox dye to its reduced form.
The amount of reducing agent dispensed on the substrate 24 is that amount able to convert, in situ, the oxidized form of redox dye on the substrate 24 into a predetermined amount of its reduced form. As discussed earlier the predetermined amount of the reduced form of the redox dye is determined in accordance with the oxygen transmission rate into the receptacle 12 (
At a point 128 within the housing 122 downstream of the dispensing station 124 the upper film 16 is laid over the lower film 18. The upper and lower films 16, 18 re then sealed together along their margins 20 by a heat sealer diagrammatically indicated by reference character 130, thereby forming the sealed receptacle 12. As may be appreciated from the foregoing discussion the sealed receptacle 12 formed in the manner described has therein both a predetermined metered amount of an oxidized form of a redox dye together with an effective amount of a reducing agent in an alkaline medium. The amount of reducing agent within the receptacle is that amount able to convert, in situ (i.e., within the receptacle 12), the oxidized form of redox dye into a predetermined amount of its reduced form. The predetermined amount of the reduced form of redox dye is determined in accordance with the oxygen transmission rate into the receptacle such that the color transition time of the reduced form of redox dye is able to be controlled precisely.
To accelerate the conversion of the redox dye to its reduced form the receptacle 12 can be heated in a heated zone 132 within the housing 122. The temperature in the heating zone may be below sixty degrees Celsius (60° C.).
After leaving the heated zone 132 but while still within the housing 122, the upper sheath 32 of the jacket 30 is superimposed over the lower sheath 34. This is indicated by the reference character 136. The oxygen-impermeable seal 36 between the mutually abutting edges of the upper sheath 32 and the lower sheath 34 is formed by a sealer 140.
The strip of finished time-indicating apparatuses are collected by a take-up reel 142.
As an alternative, as suggested at reference character 146, the indicia 42 may be printed directly onto the lower film 18. In this event, the need for the supply conveyor 104 to supply substrates 24 to the main processing line is obviated.
Disposing the oxidized form of a redox dye and an effective amount of a reducing agent in an alkaline medium within a sealed receptacle the conversion of the dye to its reduced form can occur in situ (i.e., within the sealed receptacle). Thus, the time-indicating apparatus 10 in accordance with the present invention can be manufactured by a high speed, high throughput manufacturing process. The amenability to such a manufacturing processes may reduce the cost of the time-indicating apparatus.
In the following Examples, the receptacle for the time-indicating apparatus is made using a high oxygen barrier plastic film (e.g., PVDC-coated PET films or heat-sealable PET film) or a polypropylene film. The dye, Cibanon Yellow GC PST (00943HF4) dye was obtained from Ciba Specialty Chemicals, High Point, N.C.. The amounts of dye, NaOH and sodium hydrosulfite (“hydro”) used in the Examples are indicated below.
The time intervals for the “elapsed time” (ET), the “color transition time” (CTT), “delay time” (DT) and “message appearance time” (MAT) are as defined in connection with
General Procedure for Preparing Time-Indicating Apparatus
Time-indicating apparatus in accordance with the present invention as hereinabove described were prepared for use in the Examples as follows:
Receptacles of the desired size (e.g., 1.5 inch×3.0 inch (3.8 cm×7.6 cm) or 1 inch×1 inch (2.5 cm×2.5 cm)) were prepared by placing two pieces of film on top of each other and double heat-sealing the bottom edge and one side edge.
A filter paper substrate was cut to the desired size, e.g., 0.375 inch (1 cm) discs or 1 inch (2.5 cm) squares.
A predetermined amount of dye solution was pipetted onto the filter paper substrate and allowed to air dry.
The dyed filter paper substrate was inserted into the receptacle and an additional edge was double heat sealed.
A solution of sodium hydrosulfite (“hydro”) in aqueous NaOH was prepared under an inert atmosphere, giving a solution with pH greater than 11.
A predetermined amount of the hydro/aqueous NaOH solution was added to the receptacle under a nitrogen purge, excess nitrogen was removed by squeezing the receptacle with a clamp, and the final edge of the receptacle was double heat-sealed.
Unless otherwise stated in the Examples below, the ratios given are weight ratios. The Cibanon Yellow GC PST (00943HF4) dye used in these examples is yellow in its oxidized form and blue or red-orange in its reduced form. In the sealed receptacle in the presence of hydro and aqueous NaOH, the dyed filter paper substrate turns from yellow to blue or red-orange in the absence of oxygen. This conversion can be accelerated by heating the receptacle briefly to a temperature less than 60° C. The elapsed time for the reduced dye to change back to its original (yellow) color is dependant on the relative amounts of NaOH, dye and hydro, and the Oxygen Transmission Rate (OTR) of the polymeric film receptacle. Manipulating these variables allows one to vary the elapsed time for color change in a controlled way within a range of a few hours to more than one month.
Since the amount of oxygen entering the receptacle will vary with both the oxygen transmission rate and the total surface area of the receptacle, the amount of redox dye and reducing agent may need to be adjusted for receptacles of less than two square inches (2 inch2; 5.08 cm2) or greater than nine square inches (9 inch2; 22.8 cm2).
A. Effect of Dye/Hydro Ratios on Elapsed Time
According to the General Procedure described above, 1 inch×1 inch (2.54 cm×2.54 cm) filter paper substrates were dyed using the weight of dye indicated in Table 1 and placed into receptacles made from biaxially oriented polypropylene film. Aqueous solutions containing selected ratios of NaOH to hydro were added and the receptacles sealed. The receptacles measured approximately 1.05 in×1.05 in (2.67 cm×2.67 cm). The receptacles were thermally sealed and kept at 23° C. and 55% relative humidity (“RH”). The Elapsed Time for each example is shown in Table 1.
Examples 1-3 demonstrate that increasing the hydro/dye ratio increased the Elapsed Time.
B. Effect of the Temperature and Hydro to NaOH Ratio on Elapsed Time
Time-indicating apparatus were made according to the General Procedure described above, using the amounts of dye, NaOH and hydro indicated in Table 2. The receptacles were made from one film of PET, coated on one side with PVDC, and one film of heat-sealable PET barrier film. (The PVDC coating faced the interior volume inside of the receptacle.) The receptacles were thermally sealed and evaluated at temperatures of 10° C., 22° C., and 30° C., 50-55% RH.
These Examples 4-6 demonstrate that the Elapsed Time is essentially independent of the hydro/NaOH ratio and that increasing the temperature decreases the Elapsed Time.
C. Effect of Hydro on Elapsed Time
Time-indicating apparatus were made according to the General Procedure described above, using the amounts of dye, hydro, and hydro/NaOH ratio indicated in Table 3. The receptacles were made from films of PET, coated on both sides with PVDC. The receptacles were thermally sealed and kept at 22° C. and 50% RH. Elapsed Time for each example is shown in Table 3.
These Examples 7-11 demonstrate that increasing the amount of hydro increases the Elapsed Time.
D. Effect of Amount of Dye on Color Transition Time and Elapsed Time
Time-indicating apparatus were made according to the General Procedure described above, using the amounts of dye, NaOH and hydro indicated in Table 4. The receptacles were made from films of biaxially oriented polypropylene. The receptacles were thermally sealed and kept at 23° C. and 55% RH. The initial perceived color was red-orange; the final perceived color was yellow. Elapsed Time for each example is shown in Table 4.
The Elapsed Times are comparable for all four examples (from 85.5 to 86.3 hours), while the Color Transition Time increased almost two-fold when the dye weight was increased from 0.05 mg to 10 mg. These results demonstrate that the Color Transition Time can be controlled independently of the Elapsed Time.
These Examples 12-15 also demonstrate that the Color Transition Time is controlled in accordance with the amount of reduced redox dye present in the receptacle. Decreasing the amount of reduced dye in the receptacle leads to a lower Color Transition Time.
E. Effect of Hydro on Color Transition Time and Message Access Time
Time-indicating apparatus were made according to the General Procedure described above, using 0.025 mg of dye, hydro/NaOH ratio=4, and the amount of NaOH indicated in Table 5. The receptacles were made from two films of PET coated on one side with PVDC. (PVDC coatings were toward the interior volume on the inside of the receptacle.) The receptacles were thermally sealed and kept at 22° C. and 50% RH. The Color Transition Time (CTT) and message appearance time (MAT) for each example are shown in Table 5.
These Examples 16-18 demonstrate that the color transition time, the message appearance time and the elapsed time all increase with increasing hydro.
These Examples 16-18 also demonstrate that increasing the amount of hydro, which functions both as a reducing agent and an oxygen scavenger, increases the Delay Time.
F. Examples of Indicator Packages Using Polypropylene Films.
Time-indicating apparatus were made according to the General Procedure described above, using 0.1 mg of dye, and the amount of hydro and the hydro/NaOH ratio indicated in Table 6. The receptacles were made from two films of unoriented polypropylene sold by Copol International Ltd, North Sydney, Nova Scotia, as CP-301 UO PP film. The receptacles were thermally sealed and kept at 23° C. and 55% RH. Color Transition Time and Message Appearance Time for each Example are shown in Table 6.
These Examples 19-21 utilize unoriented polypropylene film for the receptacle and result in relatively short CTT, MAT and ET.
These Examples 19-21 also demonstrate that increasing the amount of hydro, which functions both as a reducing agent and an oxygen scavenger, increases the Delay Time.
G. Effect of Film Type and Composition on Activation Energy
According to the General Procedure described above, disc or square shaped filter paper substrates were dyed with the weights listed for each example in Table 7 and placed in the receptacle made using the barrier films listed in Table 7. Receptacles made from two films of polypropylene are designated “PP/PP”. Receptacles made from one film of PET coated on one side with PVDC, and one film of heat-sealable PET barrier film are designated “PET-PVDC/HS-PET”.
Each receptacle measured approximately 1.05 inch×1.05 inch (2.7 cm×2.7 cm). The aqueous solution (0.1 ml) containing hydro and NaOH for each example was pipetted into the receptacle while under a nitrogen atmosphere. The receptacle was then thermally sealed and kept at 23° C. and 55% RH. Elapsed Times and Activation Energy for each example are shown in Table 7.
Those skilled in the art having the benefit of the teachings of the present invention as hereinabove set forth may effect numerous modifications thereto. Such modifications are to be construed as lying within the contemplation of the present invention, as defined by the appended claims.
This application claims priority to US provisional application Ser. Nos. 60/630842 (filed Nov. 24, 2004), 60/630843 (filed Nov. 24, 2004), and 60/630858 (filed Nov. 24, 2004). The entire disclosures of these provisional applications are incorporated herein by reference.
Number | Date | Country | |
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60630842 | Nov 2004 | US | |
60630843 | Nov 2004 | US | |
60630868 | Nov 2004 | US |