PTFE material with aggregations of nodes

Abstract
A novel polytetrafluoroethylene (PTFE) material includes a plurality of aggregates connected together by a plurality of relatively long fibrils. Each of the aggregates are formed of PTFE nodes that are connected together by relatively short fibrils. Preferably, the long fibrils have lengths of 500 to 1000 microns and the short fibrils have a lengths of 10 to 30 microns. The aggregates have densities of less than 2.0 grams per cubic centimeter which is lower than the densities of the solid PTFE nodes which have densities of about 2.0 to 2.2 grams per cubic centimeter.
Description
RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 09/918,844, filed Jul. 31, 2001, now abandoned, which is a continuation of U.S. patent application Ser. No. 09/373,348, filed August 12, 1999, now issued as U.S. Pat. No. 6,342,294, both of which are hereby incorporated by reference in their respective entireties.


STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable.


BACKGROUND OF THE INVENTION

The present invention relates generally to composite articles formed from expanded polytetrafluoroethylene (“ePTFE”) materials, and particularly to a composite article made up of a plurality of polytetrafluoroethylene (“PTFE”) components having differing expansion characteristics.


Conventional micro porous ePTFE articles are utilized for many useful articles, such as filters, fabrics, gaskets, electrical insulation and human implant devices. These ePTFE articles are typically produced by blending PTFE resin with a lubricant, compressing the blended resin into a billet, extruding the billet into an extrudate, drying the extrudate, calendering the extrudate (if desired), stretching or expanding the extrudate, and sintering the expanded extrudate to form the final article. The ePTFE article can be manufactured in any extruded shape, including sheets, tubes, rods or filaments.


The micro porous structure of known ePTFE articles is characterized by a plurality of nodes that are connected together by a plurality of fibrils. The nodes are essentially solid PTFE, having a density of about 2.0-2.2 grams per cubic centimeter, whereas the density of the expanded material is less than about 2.0 grams per cubic centimeter. Typically, the fibrils of ePTFE materials average in length from about 0.1 microns to about 100 microns, and the volume of the structure occupied by the fibrils has a density ranging from about 2.0 grams per cubic centimeter to less than 0.5 grams per cubic centimeter. The shape, size and orientation of the nodes and fibrils within the structure can be controlled by varying the expansion rate, expansion ratio, number of expansion axes and other processing parameters to yield many different structures. It is also known that properties such as the expandability and microstructure of the expanded article vary with the molecular weight, particle size and other physical characteristics of the PTFE resin. Various methods of producing ePTFE with differing physical properties are described in the literature, e.g. U.S. Pat. No. 3,953,566, to Gore, herein incorporated by reference.


For some applications it is desirable to provide an article having an asymmetric microstructure in which the fibrils adjacent one surface of the article are relatively short in comparison to the fibrils disposed adjacent the opposite surface of the article. However, attempted solutions to this technical problem have been unsatisfactory due to cost and functionability considerations.


BRIEF SUMMARY OF THE INVENTION

It is an object of the present invention to overcome the technical problems found in conventional ePTFE articles exhibiting asymmetric microstructures, and to provide a composite material that is made up of a plurality of PTFE components having differing expansion characteristics and that possesses an advantageous asymmetric microstructure.


In accordance with these and other objects of the present invention, a multi-layered article, such as a sheet, film or tube, of ePTFE is provided which includes at least two different component layers. At least one of the layers includes anode-fibril structure presenting substantially full-density nodes that are connected together by a first plurality of relatively short fibrils. At least one additional layer of the article includes a plurality of aggregates connected together by a plurality of relatively long fibrils having an average length of greater than about 100 microns. Each of the aggregates are formed of ePTFE including substantially full density nodes that are connected together by a second plurality of relatively short fibrils. Preferably, the short fibrils have an average length of 10-100 microns. A method of producing the article includes the steps of extruding a first PTFE material to form a first extrudate, and extruding a second PTFE material to form a second extrudate, wherein the first PTFE material is highly expandable relative to the second PTFE material. A stack is formed from at least one layer of the first extrudate and at least one layer of the second extrudate, and the stack is expanded and sintered to form the article.


The article of the present invention includes an asymmetric structure in which the lengths of the fibrils provided in the structure are longer adjacent one surface of the article than adjacent the opposite surface. Numerous advantages are realized from this construction. For example, by providing a material comprised of at least one layer of a first PTFE material of a relatively high expandability, and at least one layer of a second PTFE material of a relatively low expandability, it is possible to provide an article having an asymmetric microstructure that varies in fibril length across the thickness of the article. As such, the article has application as a biomedical material, a filter architecture, a textile fabric, a biotech cell-culture substrate, and the like.





BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING

The preferred embodiment of the present invention is described below with reference to the attached drawing figures, wherein:



FIG. 1 is a schematic view of a first layer of a composite PTFE article constructed in accordance with the preferred embodiment, illustrating a node-fibril structure of the first layer;



FIG. 2 is a schematic view of a second layer of the composite PTFE article, illustrating an aggregate-fibril structure of the second layer;



FIG. 3 is a scanning electron microscope photograph at 25× of the second layer of the composite PTFE article, illustrating ePTFE aggregates connected to each other with relatively long fibrils;



FIG. 4 is a scanning electron microscope photograph at 500× of the composite PTFE article, illustrating the underlying node-fibril structure of the first layer;



FIG. 5 is a scanning electron microscope photograph at 1000× of the composite PTFE article, illustrating the underlying node-fibril structure of the first layer;



FIG. 6 is a scanning electron microscope photograph at 90× of the composite PTFE article, illustrating a side edge thereof;



FIG. 7 is a scanning electron microscope photograph at 500× of the composite PTFE article, illustrating a transition area between the aggregates and the long fibrils of the second layer of the article;



FIG. 8 is a scanning electron microscope photograph at 500× of the composite PTFE article, illustrating the transition area between an aggregate and the long fibrils of the second layer of the article, and depicting the node-fibril structure of the aggregate; and



FIG. 9 is a scanning electron microscope photograph at 1000× of the composite PTFE article, illustrating the node-fibril structure of an aggregate of the second layer.





DETAILED DESCRIPTION OF THE INVENTION

A composite article constructed in accordance with the preferred embodiment of the present invention is illustrated in FIG. 6, and broadly includes two component layers that are referred to herein as first and second or inner and outer layers in order to facilitate an understanding of the invention. It is understood that the layers can be reversed or provided in any other desired arrangement, and that more than one layer of either or both of the components, or of a different component, may be provided without departing from the scope of the present invention.


As described in detail below, the article of the present invention is formed of at least two different PTFE components having differing expansion properties. These components are extruded separately, stacked in layers, brought into intimate contact by means of calendering or compressing in a press or die, expanded, and finally sintered. The resulting article has an asymmetric fibril structure, a unique macro-structure, and a unique micro-structure.


The individual components of the inventive article may be brought into intimate contact by any known means, such as by calendering the layered sheets together or by compressing layered sheets in a press or die. While the methods detailed herein illustrate a process for making a composite sheet material, it is not intended to limit the scope of the present invention to sheet materials. Other useful articles, such as rods, tubes, or other layered configurations can be made in a similar manner.


The multi-layered sheet is preferably comprised of two or more layers of separately extruded resins of differing expandability, referred to herein as type H and type L tapes, wherein type H tapes are those exhibiting an expansion characteristic that renders the material more highly expandable than a type L tape. These tapes are stacked in layers, brought into intimate contact by means such as a press or by calendaring, expanded below the crystalline melt point of PTFE, and then sintered.


Examples of expansion characteristics that render the PTFE more or less expandable than another include the molecular weight of the PTFE resin, the particle sizes in the PTFE resin, the lubricant level during extrusion, the dryness of expanded resin, the dye configuration during extrusion, calendering, and expansion conditions including temperature, expansion rates, and expansion speeds. Thus, a PTFE resin with a relatively high molecular weight might be selected to form the layer with the intended higher expandability, whereas a PTFE resin with a lower molecular weight might be selected to form the less expandable layer. Similarly, a PTFE resin with relatively large particle sizes could be selected to make one layer more expandable, whereas a PTFE resin with relatively small particle sizes might be selected to form the layer with the lesser expandability.


A specific formulation of PTFE paste can be produced by extruding a material that is highly expandable (hereinafter referred to as “type H”). The expanded sintered articles produced from this type H material have a normal node and fibril structure as is known, with fibrils typically ranging from about 5 microns to about 10 microns. An extrudate sheet produced from a different formulation of PTFE paste (hereinafter referred to as “type L”) can produce a PTFE material that is not as highly expandable. The expanded sintered articles produced from this type L material are difficult to make without fracturing, but when made the structure is a typical node-fibril configuration as is conventional.


When type H and L stacked tapes are expanded together at relatively high expansion ratios, the type H component of the article has unexpectedly long fibril lengths, ranging from about 10 to 30 microns. The L type component does not fracture as it would if expanded alone under the given expansion conditions. Instead, it forms a unique large scale aggregate-fibril structure including aggregates having diameters ranging in size from about 500 to 1000 microns, and fibrils connecting the aggregates together and ranging in average length from about 100 to 1000 microns, and preferably from about 500 to 1000 microns. The aggregates, rather than being essentially solid, are actually composed of a fine scale node-fibril structure, with nodes ranging in size from about 10 microns×10 microns and fibrils ranging in average length from about 10 to 30 microns. Thus, the large scale nodes have a density of less than full density, i.e. less than about 2.0 grams per cubic centimeter, while the fine scale nodes are understood to have a density of about 2.0 to 2.2 grams per cubic centimeter as is known in prior art.


The article of the preferred embodiment has two key characteristics. First, the node-fibril structure of the layer or layers formed from the more expandable type H tape is similar to the node-fibril structure known in the prior art. That is, the nodes are essentially solid PTFE, having a density of about 2.0 to 2.2 grams per cubic centimeter. However, the structure of the layer or layers formed from the less expandable type L tape has a large-scale structure of aggregates and fibrils, not similar in appearance to the previously known node-fibril structures. Further, the large-scale aggregates are actually composed of smaller nodes and fibrils; hence the large scale aggregates have a density of less than about 2.0 grams per cubic centimeter. As such, each aggregate is actually comprised of ePTFE, and these aggregates are connected together by fibrils of a length substantially longer than the fibrils defining the fine scale node-fibril structure of each aggregate.


A second key characteristic of the composite article of the present invention is that the fibril lengths of the two component layers differ, with the type L tape layer having unusually long fibrils connected between the aggregates, while the type H tape component layer has more typical fibril lengths. Furthermore, the type H component layer was found to have unexpected and longer fibril lengths in the composite article than would have been formed had it been expanded and sintered alone.


Turning to FIG. 1, the inner layer of the article is illustrated as including a node-fibril structure in which a plurality of nodes 10 are connected together by fibrils 12. The nodes 10 are made of high-density or non-expanded PTFE more typical to normal ePTFE and exhibit a density of about 2.0-2.2 gm/cc. The fibrils 12 of the inner layer connect the nodes together, and typically average 10-30 microns in length. FIG. 5 is a scanning electron microscope photograph at a magnification of 1000×, illustrating the node-fibril structure of the inner layer through the relatively long fibrils of the aggregate-fibril structure of the outer layer.


As shown in FIG. 2, the outer layer of the article exhibits an expanded aggregate-fibril structure including aggregates 14 connected to one another and to the inner layer by very long fibrils 16. As shown in FIG. 9, the aggregates each include a fine scale node-fibril structure that resembles the node-fibril structure of the inner layer, including a plurality of nodes 18 connected together by fibrils 20. The nodes 18 are made of high-density or non-expanded PTFE more typical to normal ePTFE and exhibit a density of about 2.0-2.2 gm/cc. The fibrils 20 within the aggregates connect the nodes 18 together, and typically average 10-30 microns in length.


As shown in FIG. 3, the relatively long fibrils are connected between the aggregates of the outer layer and average from about 500-1000 microns (about 0.5 to 1 mm) in length. In addition, as illustrated in FIG. 4, the long fibrils of the outer layer connect downward to the underlying node-fibril structure of the first or inner layer, connecting not only the aggregates to one another, but to the underlying inner layer of the article as well.


The transition area between an aggregate and the fibrils of the outer layer is illustrated in FIG. 7, and includes both the fine node-fibril structure of the aggregate and the relatively long fibrils that connect the aggregate to other aggregates. As shown in FIG. 8, the high density nodes of the node-fibril structure of the aggregate are connected together by longer and longer fibrils in the transition area, demonstrating the manner in which the material is stretched during formation to create the relatively long fibrils of the layer.


Turning to FIG. 6, the second or outer layer of the composite article is connected to the underlying or inner layer by a large number of the relatively long fibrils of the outer layer across the entire area of the article between the aggregates. The existence of this high density area of the relatively long fibrils in the absence of nodes is considered novel to the present invention, and the advantages of this construction are apparent to those of skill in the art. For example, the high number of fibrils connected between the layers ensures attachment of the outer layer to the underlying structure, enhancing overall strength, and the fibrils function as a natural and stress-dissipating region during flexure of the article.


The method of manufacturing the article of the preferred embodiment broadly includes the steps of extruding two different PTFE components to form first and second extrudates, one of which possesses an expansion characteristic that differs from the other.


A stack is formed from at least one layer of each of the different components, and is calendered to a desired thickness to form a multi-layered sheet. Subsequent to calendering, the sheet is heated in an oven to a temperature below the crystalline melt temperature to remove the mineral spirits, and dried. Thereafter, the dried sheet is expanded, e.g. by a radial expansion process or the like, and is sintered above the crystalline melt temperature of the PTFE to “lock” the structure.


As mentioned above, the suitable characteristics for the invention include a novel macro-structure of expanded ePTFE juxtaposed to a fine or small micro-structure of ePTFE. Macro-structures that exhibit about a 1 mm average fibril length connecting expanded ePTFE aggregates overlying a micro-structure of 20-30 micron fibrils connecting full density PTFE nodes can be made by heat processing the aforementioned expanded assemblies.


EXAMPLE 1

A PTFE resin was blended with a typical amount of mineral spirits (about 100 cc per pound of resin) to form a paste, and the paste was billeted, extruded and calendered in a conventional manner to make a tape of the type H PTFE component. The type H PTFE tape was then stacked into 10 layers, and the stack was calendered to a final thickness of about 0.1 inches. The multi-layered sheet resulting from the calendering step was dried in an oven to remove the mineral spirits, and dried. Thereafter, the dried sheet was radially expanded at an expansion ratio of about 5:1 and at an expansion rate of about 200%/second. The resulting first ePTFE article was sintered above the crystalline melt temperature of the PTFE to “lock” the structure.


A PTFE resin was blended with a high amount of mineral spirits (about 200 cc per pound of resin) and the paste was billeted, extruded, and calendered in a conventional manner to make a tape of the type L PTFE component. The type L PTFE tape was then stacked, calendered, dried, expanded, and sintered as described with reference to the type H PTFE tape, forming a second ePTFE article.


A stack was made of 8 sheets of the type H PTFE component, and a sheet of the type L PTFE component was added to both the top and bottom of the stack. The multi-layered stack was then calendered to a final thickness of about 0.1 inches, forming a sheet that was subsequently dried in an oven to remove the mineral spirits. The dried sheet was then radially expanded and sintered as described above with reference to the first and second ePTFE articles. The results are shown in Table 1.












TABLE 1





Expansion at
“type H”
“type L”



200%/sec
PTFE Tape
PTFE Tape
Preferred Invention


and 5:1 ratio
Material
Material
PTFE Tape Material







Result
Expanded into
Fractured
Macro-structure of



typical high density
and did not
expanded nodes



node fibril
expand.
connected by long



microstructure.

fibrils.





Superimposed over





Microstructure


Fibril Length
5-15-micron
No result.
About 1000 micron





macrostructure over





a 20-30 micron





microstructure.


Density
~0.4 gm/cc
No result.
About 0.2 gm/cc


Tensile
About 2000 psi.
No result
About 700 psi.


Strength









The physical characteristics of the preferred invention are given in Table 2.












TABLE 2









Result of expansion:
Expanded and formed




unique node-fibril




structure



Outer Structure:
Coarse “mm” structure




ePTFE; rough to the touch



Inner structure:
Fine “micron” structure




ePTFE; smooth to the




touch










Although the present invention has been described with reference to the preferred embodiment illustrated in the attached drawing, it is noted that substitutions may be made and equivalents employed herein without departing from the scope of the following claims.

Claims
  • 1. A composite expanded polytetrafluoroethylene article comprising: at least one layer of a first polytetrafluoroethylene material including a first plurality of nodes interconnected by a first plurality of short fibrils; at least one layer of a second polytetrafluoroethylene material including a plurality of aggregates of nodes and fibrils, each of the aggregates comprising a second plurality of nodes interconnected by a second plurality of short fibrils; anda plurality of long fibrils interconnecting the aggregates in the at least one layer of a second polytetrafluoroethylene material and connecting the aggregates in the at least one layer of a second polytetrafluoroethylene material with selected ones of the first plurality of nodes in the at least one layer of a first polytetrafluoroethylene material.
  • 2. The composite article of claim 1 wherein each of the first plurality of fibrils has an average length of about 10-100 microns.
  • 3. The composite article as recited in claim 1 wherein each of the second plurality of fibrils has an average length of about 10-100 microns.
  • 4. The composite article of claim 1 wherein each of the plurality of long fibrils has an average length of about 100 to 1000 microns.
  • 5. The composite article of claim 4 wherein each of the plurality of long fibrils has an average length of about 500-1000 microns.
  • 6. The composite article of claim 1 wherein the first and second plurality of short fibrils and the plurality of long fibrils are all formed by radial expansion.
  • 7. The composite article of claim 1 wherein each of the first plurality of nodes has a density of about 2.0-2.2 grams per cubic centimeter.
  • 8. The composite article of claim 1 wherein each of the plurality of aggregates has a density of less than 2.0 grams per cubic centimeter.
  • 9. The composite article of claim 1 wherein each of the second plurality of nodes has a density of about 2.0-2.2 grams per cubic centimeter.
  • 10. The composite article of claim 1 wherein the first polytetrafluoroethylene material is highly expandable relative to the second polytetrafluoroethylene material.
  • 11. The composite article of claim 10 wherein the first polytetrafluoroethylene material includes a greater molecular weight than the second polytetrafluoroethylene material such that the first polytetrafluoroethylene material is more expandable than the second polytetrafluoroethylene material.
  • 12. The composite article of claim 1 wherein the first polytetrafluoroethylene material is formed from particles of a first size and the second polytetrafluoroethylene material is formed from particles of a second size smaller than the first size such that the first polytetrafluoroethylene material is more expandable than the second polytetrafluoroethylene material.
US Referenced Citations (152)
Number Name Date Kind
3953566 Gore Apr 1976 A
4025679 Denny May 1977 A
4082893 Okita Apr 1978 A
4187390 Gore Feb 1980 A
4208745 Okita Jun 1980 A
4283448 Bowman Aug 1981 A
4304010 Mano Dec 1981 A
4332035 Mano Jun 1982 A
4385093 Hubis May 1983 A
4478665 Hubis Oct 1984 A
4482516 Bowman et al. Nov 1984 A
4650833 Sakagami et al. Mar 1987 A
4656234 Murayama et al. Apr 1987 A
4713070 Mano Dec 1987 A
4743480 Campbell et al. May 1988 A
4816339 Tu et al. Mar 1989 A
4819478 Melcher Apr 1989 A
4820787 Kataoka et al. Apr 1989 A
4824898 Sukigara et al. Apr 1989 A
4849285 Dillon Jul 1989 A
4859383 Dillon Aug 1989 A
4876051 Campbell et al. Oct 1989 A
4877661 House et al. Oct 1989 A
4902423 Bacino Feb 1990 A
4952630 Morgan et al. Aug 1990 A
5024671 Tu et al. Jun 1991 A
5026513 House et al. Jun 1991 A
5064593 Tamaru et al. Nov 1991 A
5071609 Tu et al. Dec 1991 A
5194154 Moyer et al. Mar 1993 A
5225131 Tamaru et al. Jul 1993 A
5234739 Tanaru et al. Aug 1993 A
5234751 Harada et al. Aug 1993 A
5258014 Harada et al. Nov 1993 A
5308664 House et al. May 1994 A
5330782 Kanazawa Jul 1994 A
5374473 Knox et al. Dec 1994 A
5426128 Burger et al. Jun 1995 A
5429869 McGregor et al. Jul 1995 A
5433909 Martakos et al. Jul 1995 A
5437900 Kuzowski Aug 1995 A
5453235 Calcote et al. Sep 1995 A
5462781 Zukowski Oct 1995 A
5474824 Martakos et al. Dec 1995 A
5476589 Bacino Dec 1995 A
5480711 Ruefer Jan 1996 A
5545475 Korleski Aug 1996 A
5607478 Lentz et al. Mar 1997 A
5620763 House et al. Apr 1997 A
5641566 Kranzler et al. Jun 1997 A
5665114 Weadock et al. Sep 1997 A
5688836 Yamamoto et al. Nov 1997 A
5718973 Lewis et al. Feb 1998 A
5741330 Brauker et al. Apr 1998 A
5800512 Lentz et al. Sep 1998 A
5879794 Korleski Mar 1999 A
6030694 Dolan et al. Feb 2000 A
6033758 Kocher et al. Mar 2000 A
6039755 Edwin et al. Mar 2000 A
6099791 Shannon et al. Aug 2000 A
6103172 Newman et al. Aug 2000 A
6110333 Spethmann et al. Aug 2000 A
6117555 Fujimori et al. Sep 2000 A
6127486 Burger et al. Oct 2000 A
6130175 Rusch et al. Oct 2000 A
6133165 Tamaru et al. Oct 2000 A
6143675 McCollam et al. Nov 2000 A
6149998 Hettinga Nov 2000 A
6162885 Ruefer Dec 2000 A
6177533 Woodward Jan 2001 B1
6194050 Koerber et al. Feb 2001 B1
6194074 Wiesemann et al. Feb 2001 B1
6196708 Rogers Mar 2001 B1
6207251 Balsimo et al. Mar 2001 B1
6218000 Rudolf et al. Apr 2001 B1
6228477 Klare et al. May 2001 B1
6261497 Wong et al. Jul 2001 B1
6287497 Kawachi et al. Sep 2001 B1
6312814 Kolouch Nov 2001 B1
6342294 Ruefer et al. Jan 2002 B1
6388033 Noda et al. May 2002 B2
6410084 Klare et al. Jun 2002 B1
6436533 Heffner et al. Aug 2002 B1
6451396 Zumbrum et al. Sep 2002 B1
6454744 Spohn et al. Sep 2002 B1
6479161 Araki et al. Nov 2002 B1
6500532 Ruefer et al. Dec 2002 B1
6511927 Ellis et al. Jan 2003 B1
6518360 Ausen et al. Feb 2003 B1
6518381 Kobayashi et al. Feb 2003 B2
6521697 Miura et al. Feb 2003 B2
6524334 Thompson Feb 2003 B1
6531559 Smith et al. Mar 2003 B1
6547814 Edwin et al. Apr 2003 B2
6547915 Taylor et al. Apr 2003 B2
6548612 Smith et al. Apr 2003 B2
6582113 Rogers Jun 2003 B2
6599997 Araki et al. Jul 2003 B2
6616876 Labrecque et al. Sep 2003 B1
6620190 Colone Sep 2003 B1
6638468 Hill et al. Oct 2003 B1
6673455 Zumbrum et al. Jan 2004 B2
6712919 Ruefer et al. Mar 2004 B2
6737158 Thompson May 2004 B1
20010006268 Delrosario et al. Jul 2001 A1
20010008672 Norvell et al. Jul 2001 A1
20010018096 Klare Aug 2001 A1
20010021756 Noda et al. Sep 2001 A1
20010033925 Trapp et al. Oct 2001 A1
20020001704 Ruefer et al. Jan 2002 A1
20020001705 Ruefer et al. Jan 2002 A1
20020004107 Rogers Jan 2002 A1
20020011684 Bahar et al. Jan 2002 A1
20020025747 Rock et al. Feb 2002 A1
20020031628 Zumbrum et al. Mar 2002 A1
20020045041 Dillon et al. Apr 2002 A1
20020051879 Tamai et al. May 2002 A1
20020053367 Kamikawa et al. May 2002 A1
20020076542 Kramer et al. Jun 2002 A1
20020096246 Sennet et al. Jul 2002 A1
20020124953 Sennett et al. Sep 2002 A1
20020132104 Urakami et al. Sep 2002 A1
20020140181 Werner Oct 2002 A1
20020147486 Soukup et al. Oct 2002 A1
20020161149 Kobayashi et al. Oct 2002 A1
20020169265 Kobayashi et al. Nov 2002 A1
20020197481 Jing et al. Dec 2002 A1
20020197924 Halley et al. Dec 2002 A1
20030010423 Nakakado et al. Jan 2003 A1
20030012905 Zumbrum et al. Jan 2003 A1
20030017775 Sowinski et al. Jan 2003 A1
20030054155 Nomi et al. Mar 2003 A1
20030062644 Oyama et al. Apr 2003 A1
20030062650 Martakos et al. Apr 2003 A1
20030065115 Kobayashi et al. Apr 2003 A1
20030067097 Yu et al. Apr 2003 A1
20030069343 Smith et al. Apr 2003 A1
20030088264 Spohn et al. May 2003 A1
20030102587 Kobayashi et al. Jun 2003 A1
20030104741 Kelmartin et al. Jun 2003 A1
20030109654 Kobayashi et al Jun 2003 A1
20030113546 Cho et al. Jun 2003 A1
20030118836 Lee et al. Jun 2003 A1
20030139806 Haverkost et al. Jul 2003 A1
20030204270 Berman et al. Oct 2003 A1
20030207118 Fukushi Nov 2003 A1
20030216531 Aten et al. Nov 2003 A1
20030228463 Abusleme et al. Dec 2003 A1
20030230834 Wynne et al. Dec 2003 A1
20040019167 Smith et al. Jan 2004 A1
20040038038 Yeung Feb 2004 A1
20040084304 Thompson May 2004 A1
Foreign Referenced Citations (6)
Number Date Country
2417901 Apr 1974 DE
0813331 Dec 1997 EP
1107749 May 2003 EP
11-80705 Jul 1989 JP
04-353534 Aug 1992 JP
WO9419170 Sep 1994 WO
Related Publications (1)
Number Date Country
20050153121 A1 Jul 2005 US
Continuations (2)
Number Date Country
Parent 09918844 Jul 2001 US
Child 10945520 US
Parent 09373348 Aug 1999 US
Child 09918844 US