Probe bonding method having improved control of bonding material

Information

  • Patent Grant
  • 8230593
  • Patent Number
    8,230,593
  • Date Filed
    Thursday, May 29, 2008
    16 years ago
  • Date Issued
    Tuesday, July 31, 2012
    12 years ago
  • Inventors
  • Original Assignees
  • Examiners
    • Nguyen; Donghai D.
    Agents
    • Peacock; Deborah A.
    • Updegraff; Samantha A.
    • Peacock Myers, P.C.
Abstract
In assembly of probe arrays for electrical test, a problem can arise where a bonding agent undesirably wicks between probes. According to embodiments of the invention, this wicking problem is alleviated by disposing an anti-wicking agent on a surface of the probe assembly such that wicking of the bonding agent along the probes toward the probe tips is hindered. The anti-wicking agent can be a solid powder, a liquid, or a gel. Once probe assembly fabrication is complete, the anti-wicking agent is removed. In preferred embodiments, a template plate is employed to hold the probe tips in proper position during fabrication. In this manner, undesirable bending of probes caused by introduction or removal of the anti-wicking agent can be reduced or eliminated.
Description
FIELD OF THE INVENTION

This invention relates to probe assemblies for making temporary electrical contact to devices or circuits under test.


BACKGROUND

Probes and probe arrangements for making temporary electrical contact to devices or circuits under test have been in widespread use for many years. Accordingly, many aspects of this technology have been developed. Although much of this technological development has focused on details pertaining to the probes, other aspects of probe technology have also been considered. More specifically, probes are typically attached to a probe card, or some other form of substrate, and some work has focused on improvements relating to the probe card/substrate.


For example, in U.S. Pat. No. 6,881,974, a probe card manufacturing approach which starts by forming blind holes in a substrate and filling these holes with an electrically conductive metal is considered. After subsequent processing, part of the metal in the blind holes is exposed to form the probe pins. In U.S. Pat. No. 6,259,261, a probe assembly is considered where a selector card can be employed to determine the pin pattern of the probing card. In U.S. Pat. No. 6,566,898, a multi-layer probe card substrate having an improved thermal expansion match to silicon is considered. In U.S. Pat. No. 6,586,955, a probe assembly having cavities filled with a low melting point metal, which are individually electrically connected to probe tips, is considered. By including a molten or near-molten metal section in each probe, metal fatigue in the probes can be alleviated, and cracking can be avoided or rendered less harmful by self-healing.


However, as integrated circuit technology continues to develop, it is necessary to probe at increasingly fine probe pitch (i.e., reduced probe spacing). This evolution can generate problems that have not apparently arisen in connection with electrical probing before, and which require new solutions.


SUMMARY

One such problem is shown in the example of FIGS. 1a-d. FIG. 1a shows a probe assembly 104 having probes 102 fixed in position by a bonding material 106 (e.g., epoxy). This kind of probe bonding approach has been considered in U.S. Pat. No. 7,345,492, issued to the present inventor, and incorporated herein by reference in its entirety. It has been found that a wicking problem can arise in connection with this probe bonding approach, as shown on FIG. 1b. Throughout this application, “wicking” refers to situations where bonding material ends up being disposed between probes at locations (e.g., 108 on FIG. 1b) outside the main bonding cavity of the probe assembly. This wicking is highly undesirable because it typically interferes with proper probe motion during operation.


In investigations to date, wicking has most commonly been observed in irregular probe arrays (e.g., probe array 112 on FIG. 1d), where closely spaced probes that are well-separated from other probes in the array tend to experience wicking. In general, probes having relatively large pitch (e.g., lateral spacing 175 μm or more) tend not to exhibit wicking, while regular probe arrays (e.g., probe array 110 on FIG. 1c) tend to be relatively well-behaved with respect to wicking (e.g., no wicking seen on a regular probe array having 110 μm probe pitch). However, it is expected that wicking in regular probe arrays is likely to be a problem for pitches of 100 μm or less. It is presently believed that wicking of the epoxies presently used for probe bonding occurs mainly during curing of the epoxy, because the elevated temperature for curing causes a temporary reduction in epoxy viscosity. This reduced viscosity enables the epoxy to more freely flow along the probes, thereby exacerbating the wicking problem.


According to embodiments of the invention, this wicking problem is alleviated by disposing an anti-wicking agent on a surface of the probe assembly such that wicking of the bonding agent along the probes toward the probe tips is hindered. The anti-wicking agent can be a solid powder, a liquid, or a gel. Once probe assembly fabrication is complete, the anti-wicking agent is removed. In preferred embodiments, a template plate is employed to hold the probe tips in proper position during fabrication. In this manner, undesirable bending of probes caused by introduction or removal of the anti-wicking agent can be reduced or eliminated.





BRIEF DESCRIPTION OF THE DRAWINGS


FIGS. 1
a-b show a problem that can arise in connection with probe assemblies having closely spaced probes.



FIGS. 1
c-d show examples of probe arrangements.



FIGS. 2
a-d show steps of a probe assembly fabrication sequence according to an embodiment of the invention.



FIG. 3 shows an approach for prevention of inter-probe wicking according to an alternate embodiment of the invention.



FIGS. 4
a-b show steps in a process for evaluating the suitability of anti-wicking materials for practicing embodiments of the invention.



FIG. 5 shows a probe tip template arrangement suitable for use with a preferred embodiment of the invention.





DETAILED DESCRIPTION


FIGS. 2
a-d show steps of a probe assembly fabrication sequence according to an embodiment of the invention. On FIG. 2a, a first guide plate 202 is separated from a second guide plate 204 by a spacer 206. Guide plates 202 and 204, in combination with spacer 206, form a guide plate assembly and define a bonding cavity (i.e., the region between plates 202 and 204 and surrounded by spacer 206). Guide plates 202 and 204 include holes within which probes are disposed.


More specifically, each of probes 208 has a base section and a tip section. The base and tip sections of one of the probes are shown on FIG. 2a as 212 and 210 respectively. The base sections of the probes are disposed in the guide plate holes such that the base sections of the probes pass through the bonding cavity of the guide plate assembly. By way of example, gaps between the probes and the guide plates at the holes are typically between 5 μm and 40 μm, and lateral probe spacing is typically less than about 150 μm.


Typically, the first and second guide plates have corresponding first and second hole patterns that are aligned with each other, so that substantially straight probe base sections fit into the guide plate assembly, as shown. In most cases, all of the probe tip sections face the same way relative to the guide plate assembly, also as shown.



FIG. 2
b shows the result of filling the bonding cavity with a curable bonding agent 214. Such filling can be performed by introducing the bonding agent through guide plate holes such as 205 and 207 on FIG. 2a. Suitable bonding agents include, but are not limited to: epoxies, thermally set materials, molten plastics and injection molding materials.



FIG. 2
c shows the result of the following steps:

  • a) (optional) providing a probe tip template 220 (supported by a frame 222) and engaging tip sections of probes 208 with the probe tip template (e.g., as shown on FIG. 2c) before adding the anti-wicking agent;
  • b) disposing an anti-wicking agent 218 on a surface of the guide plate assembly facing the tip sections of the probes; and
  • c) curing the bonding agent after disposing the anti-wicking agent. The cured bonding agent is referenced as 216. Typically, curing is performed by heating the probe assembly, although other curing processes can also be employed in practicing the invention. The bonding agent and curing process are preferably selected such that the bonding agent viscosity is lower during part of the curing step than before curing is initiated. This combination of properties facilitates elimination of bonding agent wicking according to embodiments of the invention, because wicking is suppressed at points in the process where it would otherwise be most likely to occur (i.e., during curing). Suitable materials for the optional probe tip template include polyimide, ceramics and metals.



FIG. 2
d shows the result of removing anti-wicking agent 218 after the bonding agent is cured (and of removing the probe tip template in cases where a probe tip template is employed). Anti-wicking agent 218 can be removed by vacuuming, and ultrasonic cleaning can be employed as a final cleaning step.


In the example of FIGS. 2a-d, anti-wicking agent 218 is a solid powder. It is important that bonding agent 214 not wick into the solid particles of anti-wicking agent 218. Various methods can be employed, individually or in combination, to reduce/prevent such wicking. For example, the particles of anti-wicking agent 218 can be compacted during deposition. Another method is to select solid powder materials having surfaces that are not wetted by the bonding agent. For example, talc and starch flour have been found to be suitable anti-wicking agents for an epoxy bonding agent. Fine powders are typically employed for the anti-wicking agent (e.g., particle size about 3 μm). A powder anti-wicking agent having ˜3 μm particles has been found to be effective for blocking epoxy wicking through probe to guide plate gaps of about 20 μm. A syringe capable of delivering the solid particles (i.e., having a needle bore substantially larger than the particle size) has been found suitable for delivering and compacting the anti-wicking agent. A commercial programmable epoxy dispenser can be adapted to control the amount of applied anti-wicking powder.



FIG. 3 shows a fabrication step relating to an alternate embodiment of the invention. FIG. 3 corresponds to FIG. 2c, except that a gel or liquid anti-wicking agent 302 is used on FIG. 3 instead of the solid powder anti-wicking agent of FIG. 2c. In order for a gel or liquid to function properly as an anti-wicking agent, it is preferred that the anti-wicking agent and the bonding agent be immiscible. Suitable gel or liquid anti-wicking agents for practicing embodiments of the invention include silicone based gels and lithography compatible masking fluids. After the bonding agent is cured, the anti-wicking agent can be removed by standard lithographic processes, and accordingly it is preferred for gel or liquid anti-wicking agents to be removable in this manner. In situations where probe assembly fabrication is performed in a clean room environment, it is preferred for the anti-wicking agent to be a gel or a liquid, as opposed to a powder.



FIGS. 4
a-b show steps in a process for evaluating the suitability of anti-wicking materials for practicing embodiments of the invention. In this method, a drop of uncured bonding agent 406 is disposed on a bed of a candidate material 404 on a substrate 402. The bonding agent is cured and then separated from the bed to provide a bead 408. If the surface of bead 408 is smooth and has substantially the same shape as the surface of uncured bonding agent 406 on FIG. 4a, then the bonding agent does not significantly wick into candidate material 404 as it cures, and so candidate material 404 may be a suitable anti-wicking agent. If the surface of bead 408 is rough and/or if the shape of bead 408 is substantially different than the shape of bonding agent 406 on FIG. 4a, then candidate material 404 (as prepared in this test) is not suitable for practicing embodiments of the invention. This test can be employed to evaluate the suitability of powder, liquid and gel candidate materials for practicing embodiments of the invention. It can also be used to evaluate deposition conditions, such as degree of compaction for a powdered candidate material.



FIG. 5 shows a probe tip template arrangement suitable for use with a preferred embodiment of the invention. More specifically, this figure shows a close-up view of a probe tip section 504 passing through a probe tip template 502 and having a tip 506. Preferably, tip section 504 is narrower than tip 506, as shown. The probe can move vertically with respect to the probe tip template, where tip 506 acts as a limit to keep the probe tip template from sliding off during processing. Preferably, all of the probes in the probe array have this feature which prevents the probe tip template from inadvertently sliding off the probes.


One approach for providing such a probe tip template is as follows. A probe template can be made from a polyimide sheet (e.g., 25 μm thick) with rectangular or square holes formed by laser drilling. The hole size is chosen to be slightly larger than the cross section of probe tip section 504 and slightly smaller than the cross section of probe tip 506, so the probe tip can “click” into the hole with application of a slight insertion force. After assembly and curing of the bonding agent, the template can be removed mechanically by gently pulling it off the probe tips, or chemically or via plasma etch. When mechanical removal is employed, the probe tips sometime mechanically “give” and lose alignment, so the plasma etch removal method is preferred. Plasma etching completely dissolves the polyimide template without changing probe tip alignment.

Claims
  • 1. A method for fabricating a probe assembly comprising: forming a bonding cavity;passing a plurality of probes through the bonding cavity;filling the bonding cavity with a bonding agent;disposing an anti-wicking agent on a surface of the bonding agent in the bonding cavity; andcuring the bonding agent in the bonding cavity; and removing the anti-wicking agent.
  • 2. The method of claim 1 further comprising providing a guide plate assembly having a first guide plate separated from a second guide plate by a spacer, the guide plate assembly defining the bonding cavity.
  • 3. The method of claim 2 further comprising disposing holes in the first and second guide plates.
  • 4. The method of claim 3 further comprising disposing the probes in the holes.
  • 5. The method of claim 4 further comprising providing gaps between the probes and the guide plates at the holes between 5 μm and 40 μm.
  • 6. The method of claim 4 comprising lateral spacing of the probes less than about 150 μm.
  • 7. The method of claim 3 further comprising aligning the first and second guide plates using corresponding first and second hole patterns.
  • 8. The method of claim 3 wherein the filling the bonding cavity comprises introducing the bonding agent through the holes.
  • 9. The method of claim 1 further comprising facing probe tip sections the same way relative to the guide plate assembly.
  • 10. The method of claim 1 comprising boding with a material selected from the group consisting of epoxy, thermally set material, molten plastic, and injection molding material.
  • 11. The method of claim 1 further comprising: providing a probe tip template; andengaging a tip section of each of the plurality of probes with the probe tip template prior to disposing the anti-wicking agent.
  • 12. The method of claim 11 wherein the probe tip template comprises a material selected from the group consisting of polyimide, ceramic, and metal.
  • 13. The method of claim 1 wherein curing comprises heating.
  • 14. The method of claim 1 wherein removing the anti-wicking agent comprises vacuuming out the anti-wicking agent.
  • 15. The method of claim 1 further comprising cleaning the probe assembly via ultrasonic cleaning.
  • 16. The method of claim 1 wherein the anti-wicking agent comprises a powder.
  • 17. The method of claim 16 wherein the bonding agent does not substantially wick into the powder.
  • 18. The method of claim 1 wherein the anti-wicking agent comprises talc.
  • 19. The method of claim 1 wherein the anti-wicking agent comprises starch flour.
  • 20. The method of claim 1 wherein the anti-wicking agent comprises a powder having a particle size of about 3 μm.
  • 21. The method of claim 1 further comprising compacting the anti-wicking agent.
  • 22. The method of claim 1 wherein the disposing the anti-wicking agent is performed with a syringe capable of delivering the powder.
  • 23. The method of claim 1 wherein the anti-wicking agent comprises a gel.
  • 24. The method of claim 23 wherein the gel comprises a silicone based gel.
  • 25. The method of claim 23 wherein the gel and bonding agent are substantially immiscible.
  • 26. The method of claim 1 wherein the anti-wicking agent comprises a liquid.
  • 27. The method of claim 26 wherein the liquid comprises lithography compatible masking fluid.
  • 28. The method of claim 26 wherein the liquid and bonding agent are substantially immiscible.
US Referenced Citations (228)
Number Name Date Kind
3518612 Dunman et al. Jun 1970 A
3599093 Oates Aug 1971 A
3710251 Hagge et al. Jan 1973 A
3812311 Kvaternik May 1974 A
4027935 Byrnes et al. Jun 1977 A
4115736 Tracy Sep 1978 A
4116523 Coberly et al. Sep 1978 A
4423376 Byrnes et al. Dec 1983 A
4525697 Jones et al. Jun 1985 A
4532423 Tojo et al. Jul 1985 A
4567433 Ohkubo et al. Jan 1986 A
4593961 Cosmo Jun 1986 A
4618767 Smith et al. Oct 1986 A
4618821 Lenz Oct 1986 A
4706019 Richardson Nov 1987 A
4730158 Kasai et al. Mar 1988 A
4747698 Wickramasinghe et al. May 1988 A
4757255 Margozzi Jul 1988 A
4772846 Reeds Sep 1988 A
4773877 Kruger et al. Sep 1988 A
4807159 Komatsu et al. Feb 1989 A
4901013 Benedetto et al. Feb 1990 A
4967148 Doemens et al. Oct 1990 A
5015947 Chism May 1991 A
5026291 David Jun 1991 A
5030318 Reche Jul 1991 A
5061192 Chapin et al. Oct 1991 A
5067007 Otsuka et al. Nov 1991 A
5145384 Asakawa et al. Sep 1992 A
5205739 Malo et al. Apr 1993 A
5207585 Byrnes et al. May 1993 A
5225771 Leedy Jul 1993 A
5230632 Baumberger et al. Jul 1993 A
5237743 Busacco et al. Aug 1993 A
5354205 Feigenbaum et al. Oct 1994 A
5399982 Driller Mar 1995 A
5422574 Kister Jun 1995 A
5430614 Difrancesco Jul 1995 A
5436571 Karasawa Jul 1995 A
5476211 Khandros Dec 1995 A
5531022 Beaman et al. Jul 1996 A
5576631 Stowers et al. Nov 1996 A
5632631 Fjelstad et al. May 1997 A
5635846 Beaman et al. Jun 1997 A
5644249 Kister Jul 1997 A
5676599 Ricks et al. Oct 1997 A
5701085 Malladi et al. Dec 1997 A
5720098 Kister Feb 1998 A
5742174 Kister et al. Apr 1998 A
5751157 Kister May 1998 A
5764070 Pedder Jun 1998 A
5764072 Kister Jun 1998 A
5764409 Colvin Jun 1998 A
5767691 Verkuil Jun 1998 A
5772451 Dozier, II et al. Jun 1998 A
5773987 Montoya Jun 1998 A
5802699 Fjelstad et al. Sep 1998 A
5806181 Khandros et al. Sep 1998 A
5821763 Beamann et al. Oct 1998 A
5829128 Eldridge et al. Nov 1998 A
5832601 Eldridge et al. Nov 1998 A
5847936 Forehand et al. Dec 1998 A
5852871 Khandros Dec 1998 A
5864946 Eldridge et al. Feb 1999 A
5884395 Dabrowiecki et al. Mar 1999 A
5892539 Colvin Apr 1999 A
5914613 Gleason et al. Jun 1999 A
5917707 Khandros et al. Jun 1999 A
5923178 Higgins et al. Jul 1999 A
5926951 Khandros et al. Jul 1999 A
5932323 Throssel Aug 1999 A
5934914 Fjelstad et al. Aug 1999 A
5936421 Stowers et al. Aug 1999 A
5945836 Sayre et al. Aug 1999 A
5952843 Vinh Sep 1999 A
5969533 Takagi Oct 1999 A
5970167 Colvin Oct 1999 A
5974662 Eldridge et al. Nov 1999 A
5994152 Khandros et al. Nov 1999 A
6027630 Cohen Feb 2000 A
6029344 Khandros et al. Feb 2000 A
6031282 Jones et al. Feb 2000 A
6064215 Kister May 2000 A
6066957 Van Loan et al. May 2000 A
6071630 Tomaru et al. Jun 2000 A
6086386 Fjelstad et al. Jul 2000 A
6133072 Fjelstad Oct 2000 A
6184576 Jones et al. Feb 2001 B1
6204674 Dabrowiecki et al. Mar 2001 B1
6205660 Fjelstad et al. Mar 2001 B1
6215320 Parrish Apr 2001 B1
6218203 Khoury et al. Apr 2001 B1
6246245 Akram et al. Jun 2001 B1
6246247 Eldridge et al. Jun 2001 B1
6247228 Distefano et al. Jun 2001 B1
6255126 Mathieu et al. Jul 2001 B1
6259261 Engelking et al. Jul 2001 B1
6278284 Mori et al. Aug 2001 B1
6292003 Fredrickson et al. Sep 2001 B1
6334247 Beaman et al. Jan 2002 B1
6336269 Eldridge et al. Jan 2002 B1
6344753 Takada et al. Feb 2002 B1
6411112 Das et al. Jun 2002 B1
6419500 Kister Jul 2002 B1
6420887 Kister et al. Jul 2002 B1
6424164 Kister Jul 2002 B1
6433571 Montoya Aug 2002 B1
6437584 Gleason et al. Aug 2002 B1
6441315 Eldridge et al. Aug 2002 B1
6443784 Kimoto Sep 2002 B1
6482013 Eldridge et al. Nov 2002 B2
6483328 Eldridge et al. Nov 2002 B1
6486689 Nishikawa Nov 2002 B1
6496026 Long et al. Dec 2002 B1
6525552 Kister Feb 2003 B2
6529021 Yu et al. Mar 2003 B1
6530148 Kister Mar 2003 B1
6566898 Theissen et al. May 2003 B2
6570396 Kister May 2003 B1
6573738 Matsuo et al. Jun 2003 B1
6575767 Satoh et al. Jun 2003 B2
6576485 Zhou et al. Jun 2003 B2
6586955 Fjelstad et al. Jul 2003 B2
6615485 Eldridge et al. Sep 2003 B2
6624648 Eldridge et al. Sep 2003 B2
6633176 Takemoto et al. Oct 2003 B2
6641430 Zhou et al. Nov 2003 B2
6646455 Maekawa et al. Nov 2003 B2
6676438 Zhou et al. Jan 2004 B2
6677245 Zhou et al. Jan 2004 B2
6690185 Khandros et al. Feb 2004 B1
6707311 Hohenwarter Mar 2004 B2
6727719 Liao et al. Apr 2004 B2
6731123 Kimoto May 2004 B2
6765228 Lin et al. Jul 2004 B2
6825422 Eldridge et al. Nov 2004 B2
6842023 Yoshida et al. Jan 2005 B2
6847221 Kimoto et al. Jan 2005 B2
6853208 Okubo et al. Feb 2005 B2
6881974 Wood et al. Apr 2005 B2
6890185 Kister et al. May 2005 B1
6897666 Swettlen et al. May 2005 B2
D507198 Kister Jul 2005 S
6917102 Zhou et al. Jul 2005 B2
6917525 Mok et al. Jul 2005 B2
D510043 Kister Sep 2005 S
6945827 Grube et al. Sep 2005 B2
6956389 Mai Oct 2005 B1
6965244 Miller Nov 2005 B2
6965245 Kister et al. Nov 2005 B2
6970005 Rincon et al. Nov 2005 B2
7015707 Cherian Mar 2006 B2
7036221 Higashida et al. May 2006 B2
7046021 Kister May 2006 B2
7059865 Kister et al. Jun 2006 B2
7064564 Kister et al. Jun 2006 B2
D525207 Kister et al. Jul 2006 S
7071715 Shinde et al. Jul 2006 B2
7073254 Eldridge et al. Jul 2006 B2
7078921 Haga et al. Jul 2006 B2
7088118 Liu et al. Aug 2006 B2
7091729 Kister Aug 2006 B2
7108546 Miller et al. Sep 2006 B2
7109731 Gleason et al. Sep 2006 B2
7143500 Byrd Dec 2006 B2
7148709 Kister Dec 2006 B2
7150658 Chien Dec 2006 B1
7173441 Kister et al. Feb 2007 B2
7189078 Kister et al. Mar 2007 B2
7202682 Cooper et al. Apr 2007 B2
7217138 Kister et al. May 2007 B2
7218127 Cooper et al. May 2007 B2
7218131 Tanioka et al. May 2007 B2
7225538 Eldridge et al. Jun 2007 B2
7227371 Miller Jun 2007 B2
7265565 Chen et al. Sep 2007 B2
7274195 Takemoto et al. Sep 2007 B2
7281305 Iyer et al. Oct 2007 B1
7285966 Lee et al. Oct 2007 B2
7312617 Kister Dec 2007 B2
7345492 Kister Mar 2008 B2
7417447 Kister Aug 2008 B2
7436192 Kister Oct 2008 B2
7511523 Chen et al. Mar 2009 B2
7514948 Kister Apr 2009 B2
7649367 Kister Jan 2010 B2
7659739 Kister Feb 2010 B2
7671610 Kister Mar 2010 B2
7759949 Kister Jul 2010 B2
7786740 Kister Aug 2010 B2
20010012739 Grube et al. Aug 2001 A1
20010040460 Beaman et al. Nov 2001 A1
20020070743 Felici et al. Jun 2002 A1
20020125584 Umehara et al. Sep 2002 A1
20020153913 Okubo et al. Oct 2002 A1
20020190738 Beaman et al. Dec 2002 A1
20020194730 Shih et al. Dec 2002 A1
20030027423 Zhou et al. Feb 2003 A1
20030116346 Forster et al. Jun 2003 A1
20040036493 Miller Feb 2004 A1
20040046579 Chraft et al. Mar 2004 A1
20040104737 Haga et al. Jun 2004 A1
20040119485 Koch et al. Jun 2004 A1
20040239352 Mizoguchi Dec 2004 A1
20050012513 Cheng et al. Jan 2005 A1
20050179458 Chen et al. Aug 2005 A1
20050184743 Kimura Aug 2005 A1
20050189955 Takemoto et al. Sep 2005 A1
20050189958 Chen et al. Sep 2005 A1
20060033516 Rincon et al. Feb 2006 A1
20060040417 Eldridge et al. Feb 2006 A1
20060073712 Suhir Apr 2006 A1
20060082380 Tanioka et al. Apr 2006 A1
20060170440 Sudin Aug 2006 A1
20060171425 Lee et al. Aug 2006 A1
20070145989 Zhu et al. Jun 2007 A1
20070167022 Tsai et al. Jul 2007 A1
20080074132 Fan et al. Mar 2008 A1
20090201041 Kister Aug 2009 A1
20100109691 Kister May 2010 A1
20100176832 Kister Jul 2010 A1
20100182030 Kister Jul 2010 A1
20100182031 Kister Jul 2010 A1
20100289512 Kister Nov 2010 A1
20110006796 Kister Jan 2011 A1
20110062978 Kister Mar 2011 A1
20110273198 Kister Nov 2011 A1
20110273199 Kister Nov 2011 A1
Foreign Referenced Citations (16)
Number Date Country
4237591 May 1994 DE
0144682 Jun 1985 EP
0764352 May 2004 EP
63-307678 Dec 1988 JP
01128535 May 1989 JP
7-021968 Jan 1995 JP
7-333232 Dec 1995 JP
10-506238 Jun 1998 JP
10-221374 Aug 1998 JP
11241690 Aug 1999 JP
WO 8704568 Jul 1987 WO
WO9210010 Jun 1992 WO
WO 9615458 May 1996 WO
WO9637332 Nov 1996 WO
WO9743653 Nov 1997 WO
WO0109623 Feb 2001 WO
Related Publications (1)
Number Date Country
20090293274 A1 Dec 2009 US