CA2048343A1 - Microwave active coating material including a nitrocellulose or ethyl cellulose resin - Google Patents
Microwave active coating material including a nitrocellulose or ethyl cellulose resinInfo
- Publication number
- CA2048343A1 CA2048343A1 CA 2048343 CA2048343A CA2048343A1 CA 2048343 A1 CA2048343 A1 CA 2048343A1 CA 2048343 CA2048343 CA 2048343 CA 2048343 A CA2048343 A CA 2048343A CA 2048343 A1 CA2048343 A1 CA 2048343A1
- Authority
- CA
- Canada
- Prior art keywords
- coating material
- microwave active
- material according
- conductive particles
- electrically conductive
- 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.)
- Abandoned
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 82
- 239000000463 material Substances 0.000 title claims abstract description 81
- 239000011248 coating agent Substances 0.000 title claims abstract description 76
- 239000011347 resin Substances 0.000 title claims abstract description 30
- 229920005989 resin Polymers 0.000 title claims abstract description 30
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 239000001856 Ethyl cellulose Substances 0.000 title claims abstract description 21
- 235000019325 ethyl cellulose Nutrition 0.000 title claims abstract description 20
- 229920001249 ethyl cellulose Polymers 0.000 title claims abstract description 20
- 239000000020 Nitrocellulose Substances 0.000 title claims abstract description 19
- 229920001220 nitrocellulos Polymers 0.000 title claims abstract description 19
- 239000011230 binding agent Substances 0.000 claims abstract description 23
- 239000002904 solvent Substances 0.000 claims abstract description 23
- 238000007639 printing Methods 0.000 claims abstract description 14
- 239000002245 particle Substances 0.000 claims description 33
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 22
- 229910052759 nickel Inorganic materials 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- 229910001092 metal group alloy Inorganic materials 0.000 claims description 2
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- 230000000996 additive effect Effects 0.000 claims 2
- 238000001035 drying Methods 0.000 claims 1
- 238000011065 in-situ storage Methods 0.000 claims 1
- 238000010022 rotary screen printing Methods 0.000 claims 1
- 239000003607 modifier Substances 0.000 abstract description 15
- 239000000758 substrate Substances 0.000 abstract description 15
- 239000012799 electrically-conductive coating Substances 0.000 abstract 1
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- YKYONYBAUNKHLG-UHFFFAOYSA-N propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 7
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
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- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
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- 239000000203 mixture Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 2
- 229940011051 isopropyl acetate Drugs 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- -1 propyl alcohols Chemical class 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Natural products C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- CYUOWZRAOZFACA-UHFFFAOYSA-N aluminum iron Chemical compound [Al].[Fe] CYUOWZRAOZFACA-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 229960002598 fumaric acid Drugs 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
- Paints Or Removers (AREA)
Abstract
A MICROWAVE ACTIVE COATING MATERIAL INCLUDING
A NITROCELLULOSE OR ETHYL CELLULOSE RESIN
ABSTRACT OF THE INVENTION
A microwave active coating material is provided which includes electrically conductive elements and a binder system.
The binder system includes a nitrocellulose or ethyl cellulose resin and a solvent. The coating material is capable of pattern coating a substrate to form a plurality of discrete electrically conductive elements. The discrete electrically conductive elements have a maximum dimension sufficiently small to obviate arcing. In addition, the elements form an array which operates as a microwave field modifier. The modifier may constitute a dielectric substrate having a plurality of discrete surface areas which are coated with an electrically conductive coating material to form discrete electrically conductive elements, and which discrete elements on a given surface are disposed in a predetermined array. Preferably the elements are elongate; and, preferably, the array constitutes a plurality of rows of linearly aligned elements which rows are in parallel relation, and in which the elements in adjacent rows are in staggered relation. The electrically conductive elements are preferably formed by printing an electrically conductive ink-like coating material on the dielectric substrate.
A NITROCELLULOSE OR ETHYL CELLULOSE RESIN
ABSTRACT OF THE INVENTION
A microwave active coating material is provided which includes electrically conductive elements and a binder system.
The binder system includes a nitrocellulose or ethyl cellulose resin and a solvent. The coating material is capable of pattern coating a substrate to form a plurality of discrete electrically conductive elements. The discrete electrically conductive elements have a maximum dimension sufficiently small to obviate arcing. In addition, the elements form an array which operates as a microwave field modifier. The modifier may constitute a dielectric substrate having a plurality of discrete surface areas which are coated with an electrically conductive coating material to form discrete electrically conductive elements, and which discrete elements on a given surface are disposed in a predetermined array. Preferably the elements are elongate; and, preferably, the array constitutes a plurality of rows of linearly aligned elements which rows are in parallel relation, and in which the elements in adjacent rows are in staggered relation. The electrically conductive elements are preferably formed by printing an electrically conductive ink-like coating material on the dielectric substrate.
Description
20~8343 A MICROWAVE ACTIVE COATING MATERIAL INCLUDING
- A NITROCELLULOSE OR ETHYL CELLULOSE RESIN
BACKGROUND OF THE INVENTION
1. Field of the Invention The present invention relates to microwave susceptible coating materials, and more particularly, to such coating materials useful for creating patterned microwave field modifiers.
- A NITROCELLULOSE OR ETHYL CELLULOSE RESIN
BACKGROUND OF THE INVENTION
1. Field of the Invention The present invention relates to microwave susceptible coating materials, and more particularly, to such coating materials useful for creating patterned microwave field modifiers.
2. DescriDtion of the Prior Art i Microwave ovens possess the ability to heat, cook or bake items, particularly ~ foodstuffs, extremely rapidly.
Unfortunately, microwave heating also has its disadvantages. For example~ microwave heating alone in today's microwave ovens often fails to achieve such desirable results as evenness, uniformity, browning, crispening, and reproducibility. Contemporary approaches to achieving these and other desirable results with microwave ovens include the use of microwave field modifying devices such as microwave susceptors and/or microwave shields.
Microwave susceptors and shields, like other materials and constructions have some degree of microwave reflectance (R), absorbance (A) and transmittance (T); or collectively RAT
properties. RAT properties are measured in terms of percentage of microwave energy reflected by (R), absorbed by (A), and transmitted through (T) a material or con~truction. Thus, the aggregate of the R, A and T values will total 100%.
Generically, a microwave shield is relatively opaque to microwave energy. In terms of RAT, a shield will have a relatively low T value. Microwave shields are exemplified by such highly electrically conductive materials as aluminum foil.
Although shields are generally thought of as non-heating elements, a shield could also be a susceptor, i.e., heat appreciably, and visa-versa. Thus, a shield is an element with relatively low transmittance regardless of its tendency to generate heat.
Generically, microwave susceptors are devices which, when disposed in a microwave energy field such as exists in a microwave oven, respond by generating a significant amount of 204~343 heat. The susceptor absorbs a portion of the microwave energy and converts it directly to heat which is useful, for example, to crispen or brown foodstuffs. Thus, microwave susceptors generally have a relatively high microwave absorbance value. In addition to high absorbance, susceptors include a mechanism to convert the absorbed microwave energy to heat. For example, heat may result from microwave induced, intramolecular or intermolecular action;
or from induced electrical currents which result in so called I-squared-R losses in electrically conductive devices; or from dielectric heating of dielectric material disposed between eléctrically conductive particles, elements or areas which type of heating is hereinafter alternatively referred to as fringe field heating or capacitive heating.
As noted, microwave susceptors and shields, and other materials and constructions, have an effect on the microwave power distribution within a microwave oven. That is, they interact with the microwave energy within the oven through their RAT properties and cause the microwave energy field to be modified. Accordingly, devices and constructions which act to modify the microwave field or microwave energy power distribution within a microwave oven are referred to herein collectively as microwave field modifiers.
U.S. Patent 4,914,266 discloses a microwave susceptor which is created by coating a coating material. The coating material includes carbon or graphite and an ink vehicle. The ink vehicle comprises a resin and a solvent. The resins include polymeric resins soluble in alcohol but insoluble in water such as nitrocellulose, cellulose acetate, methyl cellulose, ethyl cellulose and cellulose acetate butyrate. The solvent is alcohol which comprehends allyl, amyl, benzyl, butyl, cetyl, isopropyl and propyl alcohols.
SUMMARY OF THE INVENTION
In accordance with one aspect of the present invention a coat~ng material is provided which is microwave active when dry.
The coating material includes electrically conductive particles and a binder system. The binder system comprehends a solvent and a nitrocellulose or ethyl cellulose binder. The coating material is preferably susceptible of being coated on a substrate by means 20'1~343 of a high speed pattern coating process. The coating material preferably dries forming discrete electrically conductive elements having a conductivity, expressed in terms of resistivity, of less than about 100 ohms per square.
BRIEF DESCRIPTION OF THE DRAWINGS
While the specification concludes with claims which particularly point out and distinctly claim the invention, it is believed the present invention will be better understood from the following description of a preferred embodiment taken in conjunction with the accompanying drawings, in which like reference numerals identify identical elements and wherein;
Figure 1 is a perspective view of a preferred embodiment of a microwave field modifier which can be made using the coating material of the present invention; and Figure 2 is an enlarged scale, fragmentary portion of the microwave field modifier shown in Figure 1.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The coating material of the present invention generally includes a binder system, which comprehends either ethyl cellulose or nitrocellulose resin material and a solvent, and electrically conductive particles. In addition, the coating material may include various other components.
The binder system is used to bind the electrically conductive particles together in contacting relation. The binder system also preferably functions to bind the coating material to the dielectric substrate. Included in the binder system is a solvent and nitrocellulose or ethyl cellulose.
Typical solvents of ethyl cellulose and nitrocellulose include alcohols. "Alcohol" is commonly used to mean ethyl alcohol (or ethanol) but also may include allyl, amyl, benzyl, butyl, cetyl, methyl, n-butyl, isobutyl, isopropyl, and propyl alcohols. Nitrocellulose is also soluble in toluene, xylene and n-butyl acetate, ethyl acetate, n-propyl acetate, isopropyl acetate, and cellosolve acetate.
Unfortunately, microwave heating also has its disadvantages. For example~ microwave heating alone in today's microwave ovens often fails to achieve such desirable results as evenness, uniformity, browning, crispening, and reproducibility. Contemporary approaches to achieving these and other desirable results with microwave ovens include the use of microwave field modifying devices such as microwave susceptors and/or microwave shields.
Microwave susceptors and shields, like other materials and constructions have some degree of microwave reflectance (R), absorbance (A) and transmittance (T); or collectively RAT
properties. RAT properties are measured in terms of percentage of microwave energy reflected by (R), absorbed by (A), and transmitted through (T) a material or con~truction. Thus, the aggregate of the R, A and T values will total 100%.
Generically, a microwave shield is relatively opaque to microwave energy. In terms of RAT, a shield will have a relatively low T value. Microwave shields are exemplified by such highly electrically conductive materials as aluminum foil.
Although shields are generally thought of as non-heating elements, a shield could also be a susceptor, i.e., heat appreciably, and visa-versa. Thus, a shield is an element with relatively low transmittance regardless of its tendency to generate heat.
Generically, microwave susceptors are devices which, when disposed in a microwave energy field such as exists in a microwave oven, respond by generating a significant amount of 204~343 heat. The susceptor absorbs a portion of the microwave energy and converts it directly to heat which is useful, for example, to crispen or brown foodstuffs. Thus, microwave susceptors generally have a relatively high microwave absorbance value. In addition to high absorbance, susceptors include a mechanism to convert the absorbed microwave energy to heat. For example, heat may result from microwave induced, intramolecular or intermolecular action;
or from induced electrical currents which result in so called I-squared-R losses in electrically conductive devices; or from dielectric heating of dielectric material disposed between eléctrically conductive particles, elements or areas which type of heating is hereinafter alternatively referred to as fringe field heating or capacitive heating.
As noted, microwave susceptors and shields, and other materials and constructions, have an effect on the microwave power distribution within a microwave oven. That is, they interact with the microwave energy within the oven through their RAT properties and cause the microwave energy field to be modified. Accordingly, devices and constructions which act to modify the microwave field or microwave energy power distribution within a microwave oven are referred to herein collectively as microwave field modifiers.
U.S. Patent 4,914,266 discloses a microwave susceptor which is created by coating a coating material. The coating material includes carbon or graphite and an ink vehicle. The ink vehicle comprises a resin and a solvent. The resins include polymeric resins soluble in alcohol but insoluble in water such as nitrocellulose, cellulose acetate, methyl cellulose, ethyl cellulose and cellulose acetate butyrate. The solvent is alcohol which comprehends allyl, amyl, benzyl, butyl, cetyl, isopropyl and propyl alcohols.
SUMMARY OF THE INVENTION
In accordance with one aspect of the present invention a coat~ng material is provided which is microwave active when dry.
The coating material includes electrically conductive particles and a binder system. The binder system comprehends a solvent and a nitrocellulose or ethyl cellulose binder. The coating material is preferably susceptible of being coated on a substrate by means 20'1~343 of a high speed pattern coating process. The coating material preferably dries forming discrete electrically conductive elements having a conductivity, expressed in terms of resistivity, of less than about 100 ohms per square.
BRIEF DESCRIPTION OF THE DRAWINGS
While the specification concludes with claims which particularly point out and distinctly claim the invention, it is believed the present invention will be better understood from the following description of a preferred embodiment taken in conjunction with the accompanying drawings, in which like reference numerals identify identical elements and wherein;
Figure 1 is a perspective view of a preferred embodiment of a microwave field modifier which can be made using the coating material of the present invention; and Figure 2 is an enlarged scale, fragmentary portion of the microwave field modifier shown in Figure 1.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The coating material of the present invention generally includes a binder system, which comprehends either ethyl cellulose or nitrocellulose resin material and a solvent, and electrically conductive particles. In addition, the coating material may include various other components.
The binder system is used to bind the electrically conductive particles together in contacting relation. The binder system also preferably functions to bind the coating material to the dielectric substrate. Included in the binder system is a solvent and nitrocellulose or ethyl cellulose.
Typical solvents of ethyl cellulose and nitrocellulose include alcohols. "Alcohol" is commonly used to mean ethyl alcohol (or ethanol) but also may include allyl, amyl, benzyl, butyl, cetyl, methyl, n-butyl, isobutyl, isopropyl, and propyl alcohols. Nitrocellulose is also soluble in toluene, xylene and n-butyl acetate, ethyl acetate, n-propyl acetate, isopropyl acetate, and cellosolve acetate.
A nitrocellulose is available from General Printing, Ink Division, Sun Chemical Corporation, Cleveland, Ohio as a 40%
solution of 18-25cps RS Nitrocellulose. This solution includes 17% isopropyl alcohol, 23% ethyl acetate and 20% n-propyl acetate by weight. An ethyl cellulose is available from Hercules Inc., Wilmington, Delaware under the name Ethyl Cellulose N-4.
The nitrogen percentage of the nitrocellulose is preferably from about 10% to about 14%, and more preferably from about 11% to about 13%. The ethoxy content of the ethylcellulose is,preferably from about 47% to about 48%.
The nitrocellulose or ethyl cellulose resin is dissolved in a solvent to form solutions of preferably from about 8% to about 30% by weight resin in solvent; more preferably from about 10% to about 25%; and from about 15% to about 20% is most preferred. The higher percentages are preferred for particulate carrying properties but the lower percentages are favored for achieving a favorable printing viscosity.
Electrically conductive particles which may be used to make coating materials in accordance with the present invention preferably include carbon particles and graphite particles; and even more preferably include pure metallic particles such as nickel, iron, copper, silver and tin, some metallic oxides such as tin oxide, metal alloy particles such as aluminum iron alloys.
Coating materials made with the more preferred particles are more conductive and therefore more reflective. Furthermore, the conductive particles preferably have irregular shapes; even more preferably are also relatively flat; and most preferably are also of differing shapes and sizes; all of which promote electrical contact between the elements. In addition, the conductive particles are preferably less than 25 microns in size and more preferably less than 10 microns in size; i.e., their maximum dimension.
A preferred conductive particle which has been found successful is Nickel Flake HCA-1 which may be purchased from the Novamet Company, Wyckoff, N.J. The Novamet Nickel Flake HCA-1 is a dendritic particle formed of spheroids which have been connected - - .
~a~ls3~3 together and smashed flat. Thus, a preferred conductive particle has a flattened dendritic shape.
The conductive particles preferably constitute from about 40% to about 80% by weight of the coating material; and even more preferably from about 55% to about 65% by weight of the coating material.
The viscosity of the coating material is preferably from about 50 cps to about 7000 cps. For rotogravure printing the viscosity is preferably from about 100 cps to about 175 cps as me,asured with a ~3 zahn cup. In any event the viscosity should be such that the coating material is suitable for the chosen coating process used; be it painting, spraying, printing, silkscreen printing or rotogravure printing. Achieving the desired viscosity may require the addition of resin, solvents or other additives after the initial mixing of the coating material as is commonly done in printing processes. The percentages given above as percent by weight of the resin, solvent and conductive particles are believed broad enough to cover these situations.
Viscosity, however, can sometimes be drastically affected by the addition of small quantities of various additional components. In these situations the conductive particle to resin ratio will generally remain the same. Thus, preferred ranges can also be expressed in terms of a conductive particle:resin ratio by weight. The conductive particle:resin ratio is preferably from about 2:1 to about 20:1 and even more preferably from about 4:1 to about 10:1.
Some other components which may be used as constituents of coating materials in accordance with the present invention include emulsifying agents, acids and liquid materials which will chemically unite with the other constituents of the coating material to cause the coating material to solidify after being applied in a fluidized state. In applications of coating materials which require some flexibility, the coating materials may further comprise plasticizer material. Additionally, anti-settling agents or other constituents may be included in coating material formulations.
~0~8343 The coating material may be used to create a particularly preferred microwave field modifier such as is indicated generally as 20 in Figure 1. The microwave field modifier basically includes a substrate 22 and an array formed from a plurality of discrete electrically conductive elements 24 disposed thereon. The discrete electrically conductive elements 24 are formed from pattern coating the coating material 26 to areas of the substrate 22. Among the advantages of this structure are significant cost and equipment savings relative to current thin film susceptors. It is even more preferable if the coating material is applied to the substrate 22 by printing and most preferably by rotogravure printing. Printing offers advantages such as cost and efficiency savings over other coating processes and rotogravure printing equipment is generally currently available to carton manufacturers.
The conductive elements 24 have relatively low surface resistance: preferably one-hundred (100) ohms or less per square;
more preferably ten (10) ohms or less per square; still more preferably three (3) ohms or less per square; even more preferably one (1) ohm or less per square; and most preferably one-tenth (0.1) ohm or less per square. The maximum dimension of the elements 24 is preferably less than about four centimeters and even more preferably from about lcm to about 3cm. The elements 24 preferably have an elongate portion and/or preferably are staggered relative to each other side to side as described hereinafter.
As used herein, elongate has its ordinary meaning: i.e., having a form notably long in comparison to its width.
Additionally, the elongate elements 24 described herein are preferably substantially straight albeit it is not intended to thereby exclude serpentine, wavy, and curved shapes. Also, the elongate elements 24 preferably have radiused ends as shown to lessen the propensity for electrical arcing.
Staggered relation, as used herein, is intended to include but not be limited to shapes such as elongate, square, and rectangular elements 24 which are in side by side relation but 20~83~3 which have their ends offset from one another. The offset need not be necessarily uniform throughout the array.
Achieving a dried coating having conductivity in the desired-ranges identified above is aided by certain features. For example, putting down a sufficient quantity of coating material is important. The more coating material, i.e., the thicker the coating material, the more conductive. Coating material thickness is preferably from about 0.0001 inches to about 0.003 inches and even more preferably from about 0.0005 inches to about 0.002 inches.
Additionally, an undercoating placed on the substrate prior to printing increases conductivity. Likewise, an overcoating placed over the elements increases conductivity.
Conductivity is further increased by using both an undercoating and an overcoating. If binder of the undercoating and/or overcoating uses the same solvent as the binder of the coating material conductivity is increased even further. Consequently, an undercoating or overcoating is used, more preferably an undercoating and an overcoating is used, even more preferably an undercoating or overcoating uses the same solvent as the coating material and most preferably an undercoating and overcoating uses the same solvent as the binder of the coating material.
Furthermore, increasing the acidity of the binder seems to have a beneficial effect on conductivity. The more acidic the binder the greater the conductivity. Thus, it may be beneficial to add ac;dic binder additives to the coating material, such as acid complex forming additives. While not intending to be bound it is believed the surface chemistry effects of adsorption may be providing this benefit. The adsorption may allow for closer contact of the metal particles with each other giving rise to better conductivity. Also, it is possible salts are being formed with the ox;de making the metal more free for electrical conduction.
F;gure 1 illustrates a preferred microwave field modifier, indicated generally as 20, which may be printed using the coating material of the present invention. The substrate 22 of Figure 1 is twenty point cartonboard such as is commonly 2~ 3A3 converted into such things as cartons for packaging microwaveable food products: i.e., packages which are suitable for being placed in a microwave oven to heat, cook or bake the contents of the package without removing the contents from the carton. Other exemplary substrate 22 materials include cartonboard, coated cartonboard, thermoplastic film, thermoplastic nonwovens, thermoset plastics, or ceramic.
Disposed on the substrate 22 is an array formed from a plurality of discrete electrically conductive elements 24. In Figure 1, the array extends over the entire top surface 28 of the substrate 22 except for a perimetric zone 29 which is devoid of coating material 26. The peri~metric zone 29 acts to insulate the edges of modifier 20 so as to substantially obviate arcing between the electrically conductive elements 24 and any metallic material disposed adjacent the modifier 20. Furthermore, although the array of Figure 1 extends over the entire surface of the substrate 22, the modifier may be limited to one or more zones of the substrate 22.
Referring now to the enlarged fragmentary view of Figure 2, the preferred modifier 20 of Figure 1 includes elements 24 which are uniform in size and shape except a~ some row ends, and have lengths L and widths W, respectively. Thus, the array preferably substantially comprises elements 24 which are uniformly configured. Additionally, the elements 24 are preferably linearly aligned in straight rows parallel to each other. The rows are linearly spaced apart by a distance designated SL; and side by side rows are spaced widthwise a distance designated SW. Further, the rows are in staggered relation so that side by side adjacent elements are linearly offset by a distance designated OS. The degree of stagger, in percent, of such an array is (OS/L)(100).
Examples of ethyl cellulose and Nitrocellulose based coating materials of the present invention which may be used to print a microwave field modifier similar to the one described above are as follows:
Example 1 This Example uses a 9.3 percent solution of Nitrocellulose resin. A 9.3 percent solution can be obtained by 2~4~3~3 g starting with 4.0 grams of nitrocellulose resin. To this add 4.0 grams of a plasticizer such as Hercolyn D ~hydrogenated methyl ester of rosin), available from Hercules Chemical Corp, Wilmington, Delaware. Add 35 grams of 38/28/34 mixture of isopropyl acetate/isopropyl alcohol/n-propyl acetate as a solvent, providing a total of 43 grams of the 9.3 percent solution. To this add 57 grams of Novamet nickel HCA-1 flakes; creating a 57%
nickel and 43% (9.3% resin) resin solution coating material. Thus the final solution consists of 57 grams nickel and 43 grams of 9,3/O resin solution.
This solution is then screen printed or rotogravure printed (with only minor adjustments to viscosity) in a pattern similar to that of Figure 1. The dimensions of this pattern may be as follows: end gap SL of 0.045 inches; side gap SW of 0.0275 inches; length L of 0.787 inches; width W of 0.035 inches; and a stagger of 31%.
ExamDle 2 This Example uses a 5.4 percent solution of ethyl cellulose. A 5.4 percent solution can be obtained by starting with 2.2 grams of ethyl cellulose resin. To this add 0.5 grams of an anti-settling agent such as Bentone SD2 which is available from National LEad Chemicals, Hightstown, New Jersey. Add 4.4 grams of a modifier such as Uni-Rez 7055 (fumaric-acid modified rosin ester binder), available from Union Camp Corp., Wayne, New Jersey; and 1.8 grams of a plasticizer such as Herculon-4 (hydrogenated methyl ester of rosin), available from Hercules Chemical Corp, Wilmington, Delaware. Also add 32.1 grams of n-propyl acetate as a solvent providing a 5.4 percent ethyl cellulose solution. To this add 59 grams of Novamet nickel HCA-l flakes; creating a 59%
nickel and 41% (5.4% resin) ethyl cellulose resin solution coating material. Thus the final solution consists of 59 grams nickel and 41 grams of 5.4% resin solution.
This solution is then screen printed or rotogravure printed (with only minor adjustments to viscosity) in a pattern similar to that of Figure 1. The dimensions of this pattern may be as follows: end gap SL of 0.045 inches; side gap SW of 0.0275 2~483A3 inches; length L of 0.787 inches; width W of 0.035 inches; and a stagger of 31%.
Exam~le 3 Either of the formulations of the Examples above may be rotogravure printed; requiring only minor alterations to solution viscosity through the addition of ethanol or n-propyl acetate solvent. These solutions may be rotogravure printed in a pattern similar to Figure 1. The dimensions of this pattern may be as follows: end gap SL of 0.080 inches; side gap SW of 0.040 inches;
length L of 0.787 inches; width W of 0.020 inches; and a stagger of 25%.
Although particular embodiments of the present invention have been shown and described, modification may be made to the coating material without departing from the teachings of the present invention. Accordingly, the present invention comprises all embodiments within the scope of the appended claims.
solution of 18-25cps RS Nitrocellulose. This solution includes 17% isopropyl alcohol, 23% ethyl acetate and 20% n-propyl acetate by weight. An ethyl cellulose is available from Hercules Inc., Wilmington, Delaware under the name Ethyl Cellulose N-4.
The nitrogen percentage of the nitrocellulose is preferably from about 10% to about 14%, and more preferably from about 11% to about 13%. The ethoxy content of the ethylcellulose is,preferably from about 47% to about 48%.
The nitrocellulose or ethyl cellulose resin is dissolved in a solvent to form solutions of preferably from about 8% to about 30% by weight resin in solvent; more preferably from about 10% to about 25%; and from about 15% to about 20% is most preferred. The higher percentages are preferred for particulate carrying properties but the lower percentages are favored for achieving a favorable printing viscosity.
Electrically conductive particles which may be used to make coating materials in accordance with the present invention preferably include carbon particles and graphite particles; and even more preferably include pure metallic particles such as nickel, iron, copper, silver and tin, some metallic oxides such as tin oxide, metal alloy particles such as aluminum iron alloys.
Coating materials made with the more preferred particles are more conductive and therefore more reflective. Furthermore, the conductive particles preferably have irregular shapes; even more preferably are also relatively flat; and most preferably are also of differing shapes and sizes; all of which promote electrical contact between the elements. In addition, the conductive particles are preferably less than 25 microns in size and more preferably less than 10 microns in size; i.e., their maximum dimension.
A preferred conductive particle which has been found successful is Nickel Flake HCA-1 which may be purchased from the Novamet Company, Wyckoff, N.J. The Novamet Nickel Flake HCA-1 is a dendritic particle formed of spheroids which have been connected - - .
~a~ls3~3 together and smashed flat. Thus, a preferred conductive particle has a flattened dendritic shape.
The conductive particles preferably constitute from about 40% to about 80% by weight of the coating material; and even more preferably from about 55% to about 65% by weight of the coating material.
The viscosity of the coating material is preferably from about 50 cps to about 7000 cps. For rotogravure printing the viscosity is preferably from about 100 cps to about 175 cps as me,asured with a ~3 zahn cup. In any event the viscosity should be such that the coating material is suitable for the chosen coating process used; be it painting, spraying, printing, silkscreen printing or rotogravure printing. Achieving the desired viscosity may require the addition of resin, solvents or other additives after the initial mixing of the coating material as is commonly done in printing processes. The percentages given above as percent by weight of the resin, solvent and conductive particles are believed broad enough to cover these situations.
Viscosity, however, can sometimes be drastically affected by the addition of small quantities of various additional components. In these situations the conductive particle to resin ratio will generally remain the same. Thus, preferred ranges can also be expressed in terms of a conductive particle:resin ratio by weight. The conductive particle:resin ratio is preferably from about 2:1 to about 20:1 and even more preferably from about 4:1 to about 10:1.
Some other components which may be used as constituents of coating materials in accordance with the present invention include emulsifying agents, acids and liquid materials which will chemically unite with the other constituents of the coating material to cause the coating material to solidify after being applied in a fluidized state. In applications of coating materials which require some flexibility, the coating materials may further comprise plasticizer material. Additionally, anti-settling agents or other constituents may be included in coating material formulations.
~0~8343 The coating material may be used to create a particularly preferred microwave field modifier such as is indicated generally as 20 in Figure 1. The microwave field modifier basically includes a substrate 22 and an array formed from a plurality of discrete electrically conductive elements 24 disposed thereon. The discrete electrically conductive elements 24 are formed from pattern coating the coating material 26 to areas of the substrate 22. Among the advantages of this structure are significant cost and equipment savings relative to current thin film susceptors. It is even more preferable if the coating material is applied to the substrate 22 by printing and most preferably by rotogravure printing. Printing offers advantages such as cost and efficiency savings over other coating processes and rotogravure printing equipment is generally currently available to carton manufacturers.
The conductive elements 24 have relatively low surface resistance: preferably one-hundred (100) ohms or less per square;
more preferably ten (10) ohms or less per square; still more preferably three (3) ohms or less per square; even more preferably one (1) ohm or less per square; and most preferably one-tenth (0.1) ohm or less per square. The maximum dimension of the elements 24 is preferably less than about four centimeters and even more preferably from about lcm to about 3cm. The elements 24 preferably have an elongate portion and/or preferably are staggered relative to each other side to side as described hereinafter.
As used herein, elongate has its ordinary meaning: i.e., having a form notably long in comparison to its width.
Additionally, the elongate elements 24 described herein are preferably substantially straight albeit it is not intended to thereby exclude serpentine, wavy, and curved shapes. Also, the elongate elements 24 preferably have radiused ends as shown to lessen the propensity for electrical arcing.
Staggered relation, as used herein, is intended to include but not be limited to shapes such as elongate, square, and rectangular elements 24 which are in side by side relation but 20~83~3 which have their ends offset from one another. The offset need not be necessarily uniform throughout the array.
Achieving a dried coating having conductivity in the desired-ranges identified above is aided by certain features. For example, putting down a sufficient quantity of coating material is important. The more coating material, i.e., the thicker the coating material, the more conductive. Coating material thickness is preferably from about 0.0001 inches to about 0.003 inches and even more preferably from about 0.0005 inches to about 0.002 inches.
Additionally, an undercoating placed on the substrate prior to printing increases conductivity. Likewise, an overcoating placed over the elements increases conductivity.
Conductivity is further increased by using both an undercoating and an overcoating. If binder of the undercoating and/or overcoating uses the same solvent as the binder of the coating material conductivity is increased even further. Consequently, an undercoating or overcoating is used, more preferably an undercoating and an overcoating is used, even more preferably an undercoating or overcoating uses the same solvent as the coating material and most preferably an undercoating and overcoating uses the same solvent as the binder of the coating material.
Furthermore, increasing the acidity of the binder seems to have a beneficial effect on conductivity. The more acidic the binder the greater the conductivity. Thus, it may be beneficial to add ac;dic binder additives to the coating material, such as acid complex forming additives. While not intending to be bound it is believed the surface chemistry effects of adsorption may be providing this benefit. The adsorption may allow for closer contact of the metal particles with each other giving rise to better conductivity. Also, it is possible salts are being formed with the ox;de making the metal more free for electrical conduction.
F;gure 1 illustrates a preferred microwave field modifier, indicated generally as 20, which may be printed using the coating material of the present invention. The substrate 22 of Figure 1 is twenty point cartonboard such as is commonly 2~ 3A3 converted into such things as cartons for packaging microwaveable food products: i.e., packages which are suitable for being placed in a microwave oven to heat, cook or bake the contents of the package without removing the contents from the carton. Other exemplary substrate 22 materials include cartonboard, coated cartonboard, thermoplastic film, thermoplastic nonwovens, thermoset plastics, or ceramic.
Disposed on the substrate 22 is an array formed from a plurality of discrete electrically conductive elements 24. In Figure 1, the array extends over the entire top surface 28 of the substrate 22 except for a perimetric zone 29 which is devoid of coating material 26. The peri~metric zone 29 acts to insulate the edges of modifier 20 so as to substantially obviate arcing between the electrically conductive elements 24 and any metallic material disposed adjacent the modifier 20. Furthermore, although the array of Figure 1 extends over the entire surface of the substrate 22, the modifier may be limited to one or more zones of the substrate 22.
Referring now to the enlarged fragmentary view of Figure 2, the preferred modifier 20 of Figure 1 includes elements 24 which are uniform in size and shape except a~ some row ends, and have lengths L and widths W, respectively. Thus, the array preferably substantially comprises elements 24 which are uniformly configured. Additionally, the elements 24 are preferably linearly aligned in straight rows parallel to each other. The rows are linearly spaced apart by a distance designated SL; and side by side rows are spaced widthwise a distance designated SW. Further, the rows are in staggered relation so that side by side adjacent elements are linearly offset by a distance designated OS. The degree of stagger, in percent, of such an array is (OS/L)(100).
Examples of ethyl cellulose and Nitrocellulose based coating materials of the present invention which may be used to print a microwave field modifier similar to the one described above are as follows:
Example 1 This Example uses a 9.3 percent solution of Nitrocellulose resin. A 9.3 percent solution can be obtained by 2~4~3~3 g starting with 4.0 grams of nitrocellulose resin. To this add 4.0 grams of a plasticizer such as Hercolyn D ~hydrogenated methyl ester of rosin), available from Hercules Chemical Corp, Wilmington, Delaware. Add 35 grams of 38/28/34 mixture of isopropyl acetate/isopropyl alcohol/n-propyl acetate as a solvent, providing a total of 43 grams of the 9.3 percent solution. To this add 57 grams of Novamet nickel HCA-1 flakes; creating a 57%
nickel and 43% (9.3% resin) resin solution coating material. Thus the final solution consists of 57 grams nickel and 43 grams of 9,3/O resin solution.
This solution is then screen printed or rotogravure printed (with only minor adjustments to viscosity) in a pattern similar to that of Figure 1. The dimensions of this pattern may be as follows: end gap SL of 0.045 inches; side gap SW of 0.0275 inches; length L of 0.787 inches; width W of 0.035 inches; and a stagger of 31%.
ExamDle 2 This Example uses a 5.4 percent solution of ethyl cellulose. A 5.4 percent solution can be obtained by starting with 2.2 grams of ethyl cellulose resin. To this add 0.5 grams of an anti-settling agent such as Bentone SD2 which is available from National LEad Chemicals, Hightstown, New Jersey. Add 4.4 grams of a modifier such as Uni-Rez 7055 (fumaric-acid modified rosin ester binder), available from Union Camp Corp., Wayne, New Jersey; and 1.8 grams of a plasticizer such as Herculon-4 (hydrogenated methyl ester of rosin), available from Hercules Chemical Corp, Wilmington, Delaware. Also add 32.1 grams of n-propyl acetate as a solvent providing a 5.4 percent ethyl cellulose solution. To this add 59 grams of Novamet nickel HCA-l flakes; creating a 59%
nickel and 41% (5.4% resin) ethyl cellulose resin solution coating material. Thus the final solution consists of 59 grams nickel and 41 grams of 5.4% resin solution.
This solution is then screen printed or rotogravure printed (with only minor adjustments to viscosity) in a pattern similar to that of Figure 1. The dimensions of this pattern may be as follows: end gap SL of 0.045 inches; side gap SW of 0.0275 2~483A3 inches; length L of 0.787 inches; width W of 0.035 inches; and a stagger of 31%.
Exam~le 3 Either of the formulations of the Examples above may be rotogravure printed; requiring only minor alterations to solution viscosity through the addition of ethanol or n-propyl acetate solvent. These solutions may be rotogravure printed in a pattern similar to Figure 1. The dimensions of this pattern may be as follows: end gap SL of 0.080 inches; side gap SW of 0.040 inches;
length L of 0.787 inches; width W of 0.020 inches; and a stagger of 25%.
Although particular embodiments of the present invention have been shown and described, modification may be made to the coating material without departing from the teachings of the present invention. Accordingly, the present invention comprises all embodiments within the scope of the appended claims.
Claims (20)
1. A coating material which is microwave active when dry comprising electrically conductive particles and a binder system including a solvent and either ethyl cellulose or nitrocellulose resin.
2. A microwave active coating material according to Claim 1 wherein said binder system comprises from about 8% to about 30% by weight resin in solvent.
3. A microwave active coating material according to Claim 2 wherein said binder system comprises from about 10% to about 25%
by weight resin in solvent.
by weight resin in solvent.
4. A microwave active coating material according to Claim 1 wherein said electrically conductive particles comprise from about 40% to about 80% by weight of said coating material.
5. A microwave active coating material according to Claim 2 wherein said electrically conductive particles comprise from about 40% to about 80% by weight of said coating material.
6. A microwave active coating material according to Claim 1 wherein the weight ratio of said conductive particles to said binder resin is from about 2:1 to about 20:1.
7. A microwave active coating material according to Claim 1 further comprising an acidic material additive.
8. A microwave active coating material according to Claim 5 further comprising an acidic material additive.
9. A coating material which is microwave active when dry comprising electrically conductive particles and a binder system including a solvent and a ethyl cellulose or nitrocellulose resin, said coating material having a viscosity of from about 100 cps to about 175 cps.
10. A microwave active coating material according to Claim 9 wherein said binder system comprises from about 10% to about 25%
by weight resin in solvent.
by weight resin in solvent.
11. A microwave active coating material according to Claim 1 wherein said conductive particles are selected from the group consisting of pure metallic particles, some metallic oxides, metal alloy particles, and carbon and graphite particles.
12. A microwave active coating material according to Claim 9 wherein said conductive particles are less than about 25 microns in size.
13. A microwave active coating material according to Claim 9 wherein said conductive particles have a flat shape.
14. A microwave active coating material according to Claim 11 wherein said conductive particles have a dendritic shape.
15. A microwave active coating material according to Claim 12 wherein said conductive particles are nickel flakes.
16. A microwave active coating material according to Claim 10 wherein said conductive particles are nickel flakes having a flat dendritic shape.
17. A coating material which is microwave active when dry comprising electrically conductive particles and a binder system including a nitricellulose or ethylcellulose resin and sufficient solvent to enable application of said coating material by a high speed pattern coating process and subsequent drying in situ.
18. A coating material according to Claim 14 wherein said high speed coating process is rotogravure printing.
19. A coating material according to Claim 14 wherein said high speed coating process is rotary screen printing.
20. A coating material according to Claim 14 wherein said dried coating has an electrical conductivity expressed in terms of surface resistivity of less than about 100 ohms per square.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56801090A | 1990-08-16 | 1990-08-16 | |
| US568,010 | 1990-08-16 | ||
| US61434190A | 1990-11-15 | 1990-11-15 | |
| US614,341 | 1990-11-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2048343A1 true CA2048343A1 (en) | 1992-02-17 |
Family
ID=27074643
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2048343 Abandoned CA2048343A1 (en) | 1990-08-16 | 1991-08-02 | Microwave active coating material including a nitrocellulose or ethyl cellulose resin |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2048343A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016019461A1 (en) * | 2014-08-06 | 2016-02-11 | Fpinnovations | Printing a duplex microwave interactive susceptor structure on cellulose-based substrates for sustainable microwave packaging |
-
1991
- 1991-08-02 CA CA 2048343 patent/CA2048343A1/en not_active Abandoned
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016019461A1 (en) * | 2014-08-06 | 2016-02-11 | Fpinnovations | Printing a duplex microwave interactive susceptor structure on cellulose-based substrates for sustainable microwave packaging |
| US10271387B2 (en) | 2014-08-06 | 2019-04-23 | Fpinnovations | Printing a duplex microwave interactive susceptor structure on cellulose-based substrates for sustainable microwave packaging |
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