CA1256628A

CA1256628A - Electrically conductive microspheres and compositions incorporating same

Info

Publication number: CA1256628A
Application number: CA000463244A
Authority: CA
Inventors: Wayne L. Gindrup; Rebecca R. Vinson
Original assignee: Carolina Solvents Inc
Current assignee: Carolina Solvents Inc
Priority date: 1984-05-21
Filing date: 1984-09-14
Publication date: 1989-06-27
Also published as: US4624865A; ATE41260T1; EP0162979A1; DE3477083D1; EP0162979B1; JPS60254514A; JPH0381241B2

Abstract

ABSTRACT OF THE DISCLOSURE

Electrically conductive microparticles characterized by high conductivity and low density are comprised of electrically nonconductive microspheres having an electrically conductive coating of a metal.
When dispersed in an electrically nonconductive matrix, an electrically conductive composite material is formed in which the microparticles form a network of contacting particles throughout the matrix.

Description

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The present invention relates to conductive micro-particles, their formation, and their use in a matrix of electrically nonconductive materials to produce an electrically conductive composite.
It is known that the inclusion of conductive metal particles in a matrix of electrically nonconductive material will produce a composite which is electrically conductive. Such composites rely upon particle-to-particle contact to produce a network of particles through which electrical current may flowO Typical composites rely upon particles of metals such as copper, tin, silver, gold, platinum, stainless steel, nickel, and various alloys thereof, or other conductive materials such as car-bon or carbon fibers~ These conductive particles have been mixed into polymers such as acrylics, phenolics, alkyds, rubbers, silicones, vinyls, urethanes, and other electrically nonconductive materials.
These composites all suffer from the following detrimental characteristics: (1) In materials utilizing metals as the conductive component, the metal particles are very dense compared to the polymer matrix and thus tend to separate from one another both before and during usage. (2) In materials utilizing carbon as the conduc-tive component, the amount of carbon required to produce desirable conductivity causes the resulting composite to lose desirable mechanical properties. (3) In com-positions which do not achieve good conductivity thequantity of particles that must be incorporated make them very heavy.
Accordingly, one aspect of the present invention provides electrically conductive microparticles characterized by high conductivity and low density, said microparticles comprisin~ hollow microspheres of a ceramic composition containing magnetic impurities impartin~
permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, and a plating of an electrically conductive metal uniformly covering the surface of said microspheres and imparting electrically conductive properties thereto.
The present invention further provides an electrically conductive composite material characterized by high conductivity, low density and structural integrity, the composite material comprising an electrically nonconductive matrix, and an electrically conductive network of contacting microparticles extending throughout the matrix, each of the microparticles comprisin~ a microsphere and a coating of an electrically conductive material on the surf~ce of the microsphere.
Such composites have a number o~ useful applications, a number of which will be described herein.
Additionally, a further aspect of the present invention provides a method of producing an electrically conductive bright mirror-like metal coating on the surface of microparticles comprising hollow microspheres of a ceramic composition containing magnetic impurities imparting permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, comprising dispersing the microspheres in a plating solution consisting essentially of (a) a salt of one or more me-tals selected from the group consisting of silver, copper, nickel, gold, platinum, osmium, iridium and tin; (b) a reducing sugar and (c) an organic chelating agent, and chemically reducing the metal salt to form a bright mirror-like metal coating on the surface of the microspheres.
A still further aspect of the invention provides 6 a method of produclny an electrically conductive metal ~right mirror-like coating on the surface of microparticles comprising hollow microspheres of a ceramic composition containing magnetic impurities imparting permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, comprising sensitizing the surface of the mlcrospheres by treatment with the salt of a metal selected from the group consisting of tin, platinum and palladium, and thereafter forming a bright mirror-like metal plating onto the sensitized surface by chemically reducing with a reducing sugar in the presence of an organic chelating agent a salt of one or more metals selected from the group consisting of silver, copper, nickel, gold, platinum, palladlum, osmium, iridium and tin.
It has been found in accordance with the present invention that electrically nonconductive microspheres may be coated with an extremely thin layer of metal to produce a material which can be incorporated into electrically nonconductive materials to glve composites with superior electrical conductivity. These composites have a very low density, often lower than the electrically nonconductive plastic. Additionally, the desirable mechanical properties of the composite are only slightly affected by the inclusion of metal coated microspheres.
The term "microspheres" is understood by persons skilled in the art as referring to minute low density particles in the form of hollow or porous spheres formed of plastic, glass or ceramic. They are most commonly used as fillers in solid materials such as resins to form low density high strength composite materials. The preferred microspheres for use in the presen-t invention are glass or ceramic microspheres such as those described in U.S.

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Patent~ 3,365,315; 3,699,050 and 3,796,777. Typically, they have a specific gravity on the order of 0.2 to 2 and a particle ~ize ranging from one micron to a maximum of about 500 microns. A particularly suitable microsphere has a specific ~ravity on the order of about 0.7.
It has been found in the present invention that certain ceramic microspheres such as Q-Cel Grades 100, 110, 120, 200, 300, and others from The PQ Corporation;
and Extendospheres XOL-200, CG, SG, 5F-14, and others ~rom PA Industries have ma~netic properties. The magnetic properties are attributable to the presence in the ceramic ~omposition of magnetic components such as iron, niçkel, iron oxide, ferrite or mixtures of these materials. This magnetic property enhances the tendency of the metal coated microspheres to form networks, and gives composites with exceptional electrical conductivity.
The metal coated microspheres of the present invention are advantageous in several respects. First, because of their light wei~ht, they may be included in a composite material without significantly adding to its weight, and indeed in some cases, may actually serve to advantageously reduce the density of the composite to a density less than the matrix from which the composite i5 made. Thus, the metal coated microspheres suffer none of the disadvantages of excess weight that exist where metal particles are used in such a matrix, and are also considerably less costly.
Second, the structural inte~rity and low density of the metal coated microspheres enables them to exhibit inherently good mechanical properties, both by themselves and when included in a composite material as described herein.
Additionally, the ma~netic properties which have been discovered in certain o~ the microspheres prior to concentration of silver nitrate is much higher than taught in the prior art, when the reducing agent is a sugar such as fructose or dextrose, and when a chelating a~ent is *trade marks \
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used in an amount ~lightly more than is otherwise required to ~ive a clear ~olution when added to a silver nitrate solution.
For best results, it is desirable to carry out the metal plating in a two-step operation in which the surface of the microspheres is first sensitized by treatment with a salt of a metal selected from the ~roup consi~ting of tin, platinum or palladium, followed by chemically reducin~ salts of metals selected from the group consistin~ of silver, copper, nlckel, ~old, platinum, palladium, osmium, iridium, tin or their mixture~ using a mild reducing a~ent such as a reducing sugar (e.g. fructose or dextrose).
PreDaration of Metal Coated MicrosPheres The following examples illustrate typical methods of forming the metal-plated microspheres according to embodiments of the present invention.
EXAMPLE #1 40 grams of Q-Cel 400 obtained from the ~~
Corporation were placed in a 1 liter separatory funnel with 500 milliliters water and a solution of 3 grams of stannous chloride and 3 milliliters of concentrated hydrochloric acid in 100 milliliters water was added.
This mi~ture was ~haken and those beads which settled were removed. The remaining microspheres were washed with 800 ml. tap water three times and with 200 ml. distilled water twice. The microspheres were then washed with acetone, gravity filtered, and air dried at 60C.
50 ml. of a 2% fructose solution was added to 30 1.4 grams of the above dry microsphere~ in a 300 ml.
polyethylene ~ar. A second solution was prepared by taklng 50 ml. of 2~ silver nitrate and adding 50~ by weight aqueous AMP-95 (2-amino-2-methyl-1-propanol from International Minerals and Chemical Corp.) until the solution ~ust cleared, and then addin~ a few extra drops of AMP-95. This solution was added to the 300 ml.
polyethylene ~ar and the mlx was tumbled for 45 minutes.
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, . , The microspheres were gravity filtered, washecl with tap water and air dried. ~right uniformly coated spheres were produced.
Because Q-Cel 400, when added to water, gives an alkaline solution with a pH of 10, addition of stannous chloride without additional hydrochloric acid would cause stannous hydroxide tn precipitate and give a useless product for silvering.
EXAMPLE #2 80 grams of Q-Cel 110 from the PQ Corporation were placed in a 1 liter separatory funnel with 500 ml.
tap water, shaken, and those microspheres settling were removed. To this mixture was added a solution of 4 grams stannous chloride and 6 ml. concentrated hydrochloric acid in 100 ml. water. This mix was shaken for 5 minutes and any microspheres settling were again removed. The microspheres were washed in the separatory funnel twice wlth 500 ml. tap water and twice with 200 ml. di~tilled water. This product was then air dried.
50 gram~ of the resultin~ tinned microspheres were placed in a 550 ml. polyethylene ~ar. 200 ml. of a

2% fructose solution were added, and this mixture was tumbled. For the plating, 6 grams of silver nitrate were dissolved in 150 ml. distilled water and 15 ml. of 50% by weight AMP-95 was added to give a clear solution. Thi~
silver nltrate sollltlon was added to the polyethylene jar and the mix was tumbled for 45 minutes. The microspheres were then vacuum filtered, washed with 500 ml. tap water, rin~ed with tap water, acetone, and air dried. The yield was essentially quantitative. Examination of the spheres with a microscope showed each uniformly covered with a bright mirror-like silver coating.
EXAMPLE #3 Tin-sen~itized Q-Cel 110 as prepared in E~ample 2 may be silverplated at various silver ratios.
Typically, the weight of Q-110 could be 5, 10, 20, 25 or 30 grams treated with 3 grams silver nitrate by the following procedure. The Q-110 is placecl in a 300 ml.

polyethylene ~ar and 100 ml. of 2~ fructose is added.
This mix i~ tumbled while a solution is prepared from 3 grams of silver nitrate dissolved in iO0 ml. distilled water and ~.5 ml. of 50% by weight aqueous AMP-95. A few extra drops of the AMP-95 solution are added. The tumbler is stopped while the sil~er nitrate solution is being added. Tumbling i5 continued for 45 minutes. These microspheres may be gravity or vacuum filtered, washed, and air dried. This procedure ~ave excellent results, producing silver coated microspheres having loadings of silver ranging from approximately 28% silver to 6.25%
silver. A11 spheres gave a bright shiny appearance.
EXAMPLE #4 500 grams of Q-Cel 110 were placed into a 2 gallon stainles3 steel container. A solution was prepared of 5 grams of stannous chloride and 5 ml. concentrated hydrochloric acid in 500 ml. tap water. This solution was added to the microspheres and stirred for 5 minutes.
Approximately 2 liters of tap water were then added and the mix was stirred and then allowed to sit for about 10 minutes. The microspheres which floated ~approximately 96%) were then removed and vacuum filtered. The microspheres were then washed with 2 liters tap water followed by 600 ml. of distilled water. The damp, tin-sensitized microspheres were placed in a lined gallon canalong with 65 grams of dextrose in 1300 ml. of distilled water. 64 grams of silver nitrate were then dissolved in 700 ml. distilled water. 82 ml. AMP-95 (as received from the distributor~ was added to the silver nitrate solution, producing a clear solution. This solution was added to the gallon can which was then sealed and tumbled for 4 hours. After tumbling, the microspheres were vacuum filtered and washed with tap water. Following an acetone rinse, the bright, shiny silver coated microspheres were air dried. This procedure yielded approximately 480 grams of product.
Uses of Metal Coated Microspheres .,~
.~., According to the present invention, many significant and advantageous uses may be made of the plated microspheres, of which the following are examples not intended to limit the scop2 of -the present invention:
The metal coated microspheres of the present invention may be incorporated into typical coating formulas to give electrically conductive coatings. These coating~ may be applied by brwshing, spraying, or other methods. As an example, a cellulo~e acetate butyrate lacquer was ~ixed with 20% by weight of the material as prepared in Example 4 herein and sprayed on a gla~s panel.
After drying, measurements with an ohm meter gave readings of 6 ohms with a probe spread of 8 inches or abaut 4 ohms with a probe spread of 4 inches. This coating was an effective radio frequency shield.
The metal plated microspheres may also be used to produce an electrically conductive adhesive when they are incorporated into an adhesive composition. As an example, a commercially available hot melt adhesive was melted and 30% by weight of the metal coated microspheres prepared in Example 4 herein were stirred in. Tin panels were joined with this hot melt as a separation of 1/8 inch. When cooled, the conductivity across the adhesive joint was found to be 0.1 ohm.
The metal coated microspheres may also be used to produce an electrically conductive liquîd which is suitable for the replacement of mercury in certain types of switches. A mixture of silicone oil or other electrically nonconductive liquid mixed with 30% by weight metal coated microspheres behaves as an electrically conductlve liquid and will cause a low resistance electrical circuit to be formed when placed between two electrodes.
The ~trength of the microspheres i5 sufficient to allow for in~ection molding and extrwsion. If sufficient metal coated microspheres are used, in~ection molded or extruded parts are highly electrically conductive.

In other applicatlons, the metal coated microspheres of the present invention may be sprayed to a tacky surface of paint, polymer or other similar materials to produce an electrically conductive surface.
The metal coated microspheres of the present invention al50 perform well in certain applications even without being plac~d in a polymer matrix. For example, the equivalent of an electrically conductive wire that will not break upon repeated flexing may be prepared by tightly filling a piece of rubber tubin~ with the dry metal coated microspheres. This device will maintain conductivity without breaking upon repeated flexing.
Where a thin coating of catalytic metal such as platinum i8 applied to the microspheres, a unique catalyst may be prepareA which is useful for fluidized beds, and in contrast to more den~e beads, ha~ a very low heat capacity and the pressures reguired to maintain the fluidized condltion are extremely low.
Metal coated microspheres below 50 microns in diameter may be incorporated into printing inks and pastes to produce electrically conductive printing suitable for detection by electronic means.
Electrically conductive epoxy castings and adhe~ives may be prepared by incorporating sufficient metal coated microspheres of the present invention. As an example, a two component epoxy system was prepared and 30%
by weight of the metal coated microsphere~ were ~tirred in. The mix was placed in several polyethylene containers and allowed to harden. The resulting plastic castings exhibited very good electrical conductivity.
A very unique material may be prepared by adding a self-setting system such as an epoxy, urethane, or polyester to a large amount of metal coated microspheres.
This yields a putty-like material which will 500~ harden to a very li~ht matrix with excellent mechanical and electrical properties. A similar system may also be prepared by lightly wetting the spheres with a thermosetting polymer such as a phenolic and bakin~ it.

This also yields an extra light and strong electrically conductive part.
In certaln applications, it ls advantageous for certain injection molded parts to be surface coated with a different material after molding has been completed. This may be accomplished by first spraying the mold parts with a coating before injection molding a part. According to the present invention, the coating incorporates metal coated microspheres, a part may then be injection molded which will result in a surface of any colour, texture, or strength that is electrically conductive and suitable for RF ~hieldiny.
Static electricity causes many problems in hospital operating rooms, aircraft, computer rooms, or other areas where static charges may be generated. In the past, to bleed these electrostatic charges away, plastics were produced with very high carbon contents to produce materials with ~ufficierlt conductivity to dissipate such charges. Because the percentages of carbon required was 20 80 high, the physical properties of such coatings, coverings and floorings were poor. Incorporation of electrically conduc-tive metal coated microspheres according to the present invention, however, yields conductive materials, flooring, and upholstery which retain good physical properties and have conductivities much greater than materials loaded with carbon.
Electronic printed circuit boards utilizing high speed solid state components often suffer from unwanted coupling, cross-talk, and external RF interference. The metal coated microspheres of the present invention may be used to produce the e~uivalent of a form fittlng ground plane which will completely shield the board from e~ternal fields and limit internal coupling. Such a plane may be prepared by first coating the finished board with a non-electrically conductive barrier coat and then completelyspraying the board with a suitable coating which incorporates sufficient metal coated microspheres to become electrically conductive.

., , In certain applications, coatings or castings incorporatlng sufficient metal coated microspheres of the present invention may be used in reflectors of electromagnetic radiation. As an e~ample, a concave dish made of plastic which is electrically nonconductive and transparent to mlcrowaves may be used as a microwave antenna by coating the concave surface with paint containing sufficient metal coated microspheres to make the surface electrically conductive.
For other application, a useful patching material may be prepared by adding sufficient metal coated miorospheres to a silicone rubber or the like and troweling and smoothing this mix onto such substrates as the metal plates used in complex shaped radio frequency molds.
A useful shielding material suitable for shielding telephone cables and other such electronic transmission devices may be prepared by incorporating sufficient metal coated microspheres into a mastic or putty to render the mix electrically conductive.
A useful gasket for radio frequency shielding in cable couplings may be made by incorporating sufficient metal coated microspheres to yield a conductive gasket.
A useful radio frequency shield may be prepared by incorporating sufficient metal coat~fl microspheres in heat shrinkable tubin~ to produce the equivalent of a heat shrinkable metal tube.
A more uniform, reliable, and less expensive Qwitch may be prepared by adding metal coated microspheres to a rubber, such as a silicone. In the past, pressure sensitive switches have been prepared by adding metal ~lakes or powder to a rubber in a concentration ~ust below where electrical conductivity is achieved. Upon compressin~ the rubber the particles touch and the composite becomes a good electrical conductor.
The metal flakes and powder used in the past tended to settle before the liquid silicone set to a rubber. The random particle shapes of the powder and ;.~.
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flakes also caused consistent reproducibility to be difficult to achieve. Metal coated microspheres do not have any of these deficiencies. The uniform spherical shape and no tendency to settle allow the production of switches of uniform and constant electrical ch~racteristics.
Very high static electricity charges are generated during reentry of space vehicles into the atmosphere. The metal coated microspheres of the present invention may be lncorporated into the heat shields used in space vehicles to render the heat shields electrically conductive and thereby dissipate static electricity charges.

Claims

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. Electrically conductive microparticles characterized by high conductivity and low density, said microparticles comprising hollow microspheres of a ceramic composition containing magnetic impurities imparting permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, and a plating of an electrically conductive metal uniformly covering the surface of said microspheres and imparting electrically conductive properties thereto.

2. Electrically conductive microparticles according to claim 1, wherein said microspheres have a diameter of from 1 to 500 microns and a specific gravity of 0.2 to 2.

3. Electrically conductive microparticles characterized by high conductivity and low density, said microparticles comprising hollow microspheres formed of a ceramic composition having permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, said microspheres having a diameter of between about 1 and 500 microns and a specific gravity of between about 0.2 to 2; and an electrically conductive coating of metal uniformly covering the surface of said microspheres and imparting electrical conductivity thereto, said metal being chosen from the group consisting of silver, copper, nickel, gold, platinum, palladium, osmium, iridium, and tin and alloys consisting essentially of these metals.

4. Electrically conductive microparticles according to claim 3, wherein said ceramic composition includes a magnetic material selected from the group consisting or iron, nickel, iron oxide, ferrite, or mixtures of these materials imparting magnetic properties to the microspheres.

5. Electrically conductive microparticles characterized by high conductivity and low density, said microparticles comprising hollow ceramic magnetic microspheres, said microspheres having permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, and said microspheres having a diameter of from 1 to 500 microns and a specific gravity of between about 0.2 and 2, and a bright mirror-like silver plating uniformly covering the surface of said microspheres and imparting electrical conductivity thereto.

6. Electrically conductive microparticles according to claim 1, 3 or 5, wherein said electrically conductive microparticles are dispersed in an electrically nonconductive matrix and are magnetically attracted to one another to form an electrically conductive network.

7. Electrically conductive microparticles according to claim 1, 3 or 5, wherein said electrically conductive microparticles are adhered to an electrically nonconductive base and are magnetically attracted to one another to form an electrically conductive network.

8. Electrically conductive microparticles according to claim 1, 3 or 5, wherein said electrically conductive microparticles are dispersed in an electrically nonconductive polymeric adhesive and are magnetically attracted to one another to form an electrically conductive network.

9. Electrically conductive microparticles according to claim 1, 3 or 5, wherein said electrically conductive microparticles are dispersed in an electrically nonconductive liquid and are magnetically attracted to one another to form an electrically conductive network.

10. A method of producing an electrically conductive bright mirror-like metal coating on the surface of microparticles comprising hollow microspheres of a ceramic composition containing magnetic impurities imparting permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, comprising dispersing the microspheres in a plating solution consisting essentially of (a) a salt of one or more metals selected from the group consisting of silver, copper, nickel, gold, platinum, osmium, iridium and tin;
(b) a reducing sugar and (c) an organic chelating agent, and chemically reducing the metal salt to form a bright mirror-like metal coating on the surface of the microspheres.

11. A method of producing an electrically conductive metal bright mirror-like coating on the surface of microparticles comprising hollow microspheres of a ceramic composition containing magnetic impurities imparting permanent magnet properties which render the microspheres magnetically attractive to one another to form a network of contacting particles, comprising sensitizing the surface of the microspheres by treatment with the salt of a metal selected from the group consisting of tin, platinum and palladium, and thereafter forming a bright mirror-like metal plating onto the sensitized surface by chemically reducing with a reducing sugar in the presence of an organic chelating agent a salt of one or more metals selected from the group consisting of silver, copper, nickel, gold, platinum, palladium, osmium, iridium and tin.

12. A method according to claim 10 or 11, wherein the metal salt which is chemically reduced to form said metal coating comprises silver nitrate.

13. A method according to claim 10 or 11, wherein the microspheres have a diameter between about 1 and 500 microns and a specific gravity of between 0.2 and 2.