Making particulates of controlled dimensions by electroplating

Stock material or miscellaneous articles – Web or sheet containing structurally defined element or... – Including a second component containing structurally defined...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C148S306000, C148S313000, C252S06251C, C428S402000, C428S403000, C428S935000

Reexamination Certificate

active

06376063

ABSTRACT:

TECHNICAL FIELD
The present invention relates to an electroplating method for making particulates of controlled dimensions, to the particulates themselves (especially magnetic Fe—Co ones), and to products using the particulates.
BACKGROUND OF THE INVENTION
Flat metallic particles of controlled thickness and shape typically are difficult and expensive to make. Ball milling results in relatively thick flake with little control of size and shape. Vacuum deposition followed by a chemical or mechanical removal of particulates from the substrate is costly with little control of shape of the flake. Vacuum/chemical vapor deposition of coatings onto existing particulates such as flakes (e.g., mica) or spheres produces flakes limited to the shape and size of the existing particulate. Pre-existing flake shapes are typically too thick and the shape too jagged for high performance coatings.
Thin film metal particulates are expensive, because existing process to make them, like those described in U.S. Pat. Nos. 4,879,140 or 5,100,599, use exotic equipment such as plasma generators or vacuum chambers, or are labor intensive, small scale processes like photolithography. The equipment cost and relative slow rate of production using skilled labor to operate the sophisticated equipment increases the cost. The prior art particulates are not readily produced in reasonable volume, and cost as much as $5,000/oz. At these prices, paints that use the particulates as the pigment are only suitable for highly specialized applications. There is a need for a lower cost, higher volume process for rapidly and reliably making thin film metal particulates usable as paint pigments.
In U.S. Pat. No. 5,100,599, Jensen et al. described a vapor deposition/photolithography method for making thin film particulates of controlled shape. Independent deposition sites are defined with layers of photoresist. The thin films are deposited on the sites. Then, the photoresist is dissolved to free the flakes.
In U.S. Pat. No. 5,895,524, Dickson described a method for making thin film metal particulates including the steps of immersing a metallized sheet of fluorinated ethylene propylene (FEP) first in an aqueous base and then in an aqueous acid to loosen and release the metal from the FEP. The particulates are brushed from the FEP into the acid tank, and are recovered. The FEP is reusable. The particulates are usually aluminum or germanium metal having a thickness of about 900 to 1100 Å, and preferably, 1000 Å. The method for freeing the particulates may also include ultrasonically vibrating the metallized sheet following the immersions.
For making aluminum particulates, the preferred base is 7% Na
2
CO
3
and the preferred acid is 0.01-0.1 N acetic acid. For making germanium particulates, the preferred base is 2.5 N NaOH, since this metal is harder to loosen from the FEP. The acid bath neutralizes the basic reaction between the metal film and base.
The base immersion takes about 15 seconds. Prior to the acid immersion, the base-treated metallized film is exposed to air for about 25 seconds. The acid immersion lasts about 15 seconds before brushing the particulates from the FEP. A metallized roll of the FEP is readily towed through the several operations in a continuous process, as will be understood by those of ordinary skill.
Particulates are recovered from the acid bath by filtering, rinsing, and drying. The particulates are sized. Then, as described in U.S. Pat. No. 5,874,167, the particulates are treated using conventional aluminum treatments. Suitable treatments include applying chemical conversion coatings or protective sol coatings. The conversion coatings may be chromic acid anodizing, phosphoric acid anodizing, Alodine treating (particularly using either Alodine 600 or Alodine 1200); cobalt-based conversion coating as described in Boeing's U.S. Pat. Nos. 5,298,092; 5,378,293; 5,411,606; 5,415,687; 5,468,307; 5,472,524; 5,487,949; and 5,551,994; or the like. The sol coating method creates a sol-gel film on the surface using a hybrid organozirconium and organosilane sol as described in Boeing's U.S. Pat. No. 5,849,110. Related sol-gel coated aluminum flakes are described in U.S. Pat. No. 5,261,955.
The different treatments can impart different tint to the pigment. Alodine imparts a yellow or greenish-yellow tint. The cobalt treatments impart blue tints.
The sol coating is preferable a hybrid mixture wherein the zirconium bonds to the aluminum flake covalently while the organic tail of the organosilane bonds with the paint binder. The anodizing treatments promote adhesion primarily by mechanical surface phenomena. The sol coating provides adhesion both through mechanical surface phenomena (surface microroughening) and through chemical affinity, chemical compatibility, and covalent chemical bonds.
The particulates are pigments for paints or surface coatings and generally are used in urethane, cyanate ester, or urea binders. The organosilane in the sol coating generally will include a lower aliphatic amine that is compatible with the binder.
Kenneth Suslick of the University of Illinois pioneered research into sonochemistry, a technique that uses the energy of sound to produce cavitation bubbles in a solvent. The bubbles collapse during the compression portion of the acoustic cycle with extreme microscale energy release evidenced by high (microscale) localized temperatures and pressures estimated at about 5200° F. and 1800 atm, respectively. Suslick determined that sonochemistry was an effective way to produce amorphous metal particles. He developed laboratory processes for making amorphous iron agglomerates desired as catalysts in hydrocarbon reforming, carbon monoxide hydrogenation, and other reactions.
Suslick also discovered that he could produce metal colloids and supported catalysts if he sonicated the metal precursors (principally volatile metal carbonyls or other organometallics) with a suspended polymer like polyvinylpyrrolidone or with suspended inorganic oxide supports, such as silica or alumina.
Suslick's work focused on sonochemical techniques to form catalysts composed of agglomerated metal nanoparticles. These catalysts are efficient because of their large surface areas. His work is described in the following articles that we incorporate by reference:
(1) K. Suslick, “
Sonochemistry,”
247 Science 1439-1445 (Mar. 23, 1990);
(2) K. Suslick et al., “
Sonochemical Synthesis of Amorphous Iron”,
353 Nature 414-416 (Oct. 3, 1991); and
(3) K. Suslick, “
The Chemistry of Ultrasound
,” Yearbook of Science & the Future, Encyclopedia Britannica, Inc., 138-155 (1994). Similar work is described in the following articles by Lawrence Crum, that we also incorporate by reference:
(1) L. Crum, “
Sonoluminescence
,” Physics Today, September 1994, pp. 22-29, and
(2) L. Crum “
Sonoluminescence, Sonochemistry, and Sonophysics
”, J. Acoust. Soc. Am. 95(1), January 1994, pp. 559-562.
Gibson sonicated Co
2+
(aq) with hydrazine to produce anisometric cobalt nanoclusters. Science, vol. 267, Mar. 3, 1995. He produced anisometric, hexagonal disk-shaped, cobalt nanoclusters about 100 nanometers in width and 15 nanometers in thickness with oriented (001) crystals comparable to cells of &agr;-cobalt. The nanoclusters were small enough to be strongly influenced by Brownian forces and thereby were resistant to agglomeration. Working with hydrazine, however, on a commercial scale poses safety questions.
In U.S. Pat. Nos. 5,520,717; 5,766,764; and 5,766,306, Boeing described a process to create “nanophase” or “nanoscale” amorphous metal particles with Suslick's sonochemistry techniques using organometallic precursors like iron pentacarbonyl (Fe(CO)
5
) in an alkane (like n-heptane or n-decane) under an inert atmosphere with sonication at about 20 kHz and 40-100 Watts for 0.1-24 hours. The particles (distributed in the range of about 5-100 nm in diameter) were extracted from the alkane using a polar solvent of reasonably high vapor pressure, such as ethylene glycol monomethyl ether (CH
3
O—CH
2
CH
2
—OH).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Making particulates of controlled dimensions by electroplating does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Making particulates of controlled dimensions by electroplating, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Making particulates of controlled dimensions by electroplating will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2825741

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.