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January 2006

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Subject:
From:
Clavius Chin <[log in to unmask]>
Reply To:
(Leadfree Electronics Assembly Forum)
Date:
Mon, 30 Jan 2006 09:39:11 +0700
Content-Type:
text/plain
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text/plain (299 lines)
Lee,


        Your suggestion is good. However, if the Pb layer is too thin, it
may make SEM/EDX analysis difficult. If this happens, an alternative
analysis is to perform XPS/Auger Electron Spectroscopy with sputtering.
This would be able determine the thickness distribution of Pb.



Best Regards,
Clavius Chin, Ph.D.
Failure Analysis & Lab Manager
Tel: +66-38-493561 EXT. 1249
        +66-1-9839128 (H/P)



Lee parker <[log in to unmask]>
Sent by: Leadfree <[log in to unmask]>
01/28/2006 03:50 AM
Please respond to
"(Leadfree Electronics Assembly Forum)" <[log in to unmask]>; Please respond
to
Lee parker <[log in to unmask]>


To
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cc

Subject
Re: [LF]






Don

By viewing the cross section with a SEM plus EDAX you can determine what
is on the surface or at any other point in the structure, even if you do
not want to know!

Best regards

Lee

J. Lee Parker, Ph.D.
JLP Consultants LLC
804 779 3389
  ----- Original Message -----
  From: Abbott, Don<mailto:[log in to unmask]>
  To: [log in to unmask]<mailto:[log in to unmask]>
  Sent: Friday, January 27, 2006 3:25 PM
  Subject: Re: [LF]


  Lee,
  This bring up an interesting point - if the Pb is only on the surface,
  as it is plated, then would it be considered "homogeneous" (as it can be
  mechanically removed by scraping) - in which case is would be 100% Pb
  and thus a clear violation?

  XRF may be preferable to sectioning, in light of the above.

  Regards,
  Don Abbott
  TI
  508-236-1569

  -----Original Message-----
  From: Leadfree [mailto:[log in to unmask]] On Behalf Of Lee parker
  Sent: Friday, January 27, 2006 3:17 PM
  To: [log in to unmask]<mailto:[log in to unmask]>
  Subject: Re: [LF]

  Carol

  I agree with George. XRF is only suitable for measuring the thickness of
  an identified metal. It does not tell you where in the composite the
  metal is located. An approach you may want to pursue is to make cross
  sections of the problem area (probably a pad) and then use a SEM with
  EDAX capability. Place the cross section into the SEM and then focus the
  EDAX beam at several points on the cross section starting at the surface
  and working down. You will then have an elemental analysis at several
  points and you can then determine what metals are on the surface, the
  transition region and the base material. If you do not have this
  capability on site, there are many labs across the country that do.

  Good luck

  Lee

  J. Lee Parker, Ph.D.
  JLP Consultants LLC
  804 779 3389

  ----- Original Message -----
    From: Wenger, George M.<mailto:[log in to unmask]<
mailto:[log in to unmask]>>
    To: [log in to unmask]<mailto:[log in to unmask]<mailto:[log in to unmask]<
mailto:[log in to unmask]>>
    Sent: Friday, January 27, 2006 1:36 PM
    Subject: Re: [LF]


    Carol,

    What are the units for the 0.14-0.19?  Are they percent of XRF signal
  or
    are they XRF thickness measurements?  How does the XRF analysis tell
  you
    the Pb is on top?  Do you have an XRF spectrum you can send or post on
    Steve's web page?


    Regards,
    George
    George M. Wenger
    Reliability / FMA Engineer
    Base Station and Subsystems Group
    Andrew Corporation, 40 Technology Drive, Warren, NJ 07059 (908)
  546-4531

[log in to unmask]<mailto:[log in to unmask]<mailto:[log in to unmask]<
mailto:[log in to unmask]>>

    -----Original Message-----
    From: Leadfree [mailto:[log in to unmask]] On Behalf Of Carol Spiers
    Sent: Friday, January 27, 2006 1:20 PM
    To: [log in to unmask]<mailto:[log in to unmask]<mailto:[log in to unmask]<
mailto:[log in to unmask]>>
    Subject: [LF]

    I have just had an analysis completed on a first batch run of leadfree
    boards.  Results indicate we have  uniform contamination of 0.14-0.19
    layer of lead across the board.  The testing and measurements were
    obtained using  xray flouresence and indicate the lead is on the top
    layer of the melded solder.  We confirmed that all parts were
  documented
    as being Lead Free (but not tested by us for compliance).  Boards were
    double sided silver immersion smt and thru hole combinations.  Solder
    paste used was SAC, wave solder bar used was SAC.  The wave solder
    machine is brand new (never used in a leaded process).  SMT oven is
  used
    for both leaded and unleaded processes.
    Because the contamination appears to be uniformly spread across the
    board I tend to think this isn't a problem related to a couple of
    components not actually being lead free and contiminating the huge pot
    of solder in the wave.  One suggestion was that there might have been
  a
    thin layer of lead over top of the silver immersion on the bare
  boards.

    Is there anyone out there that would care to offer some suggestions as
    to where we should focus our investigation or if any alternative
  testing
    should be used.
    So far we are going to:
    1) do comparison testing of two batches of bare boards of the same
    product coming from different suppliers and undergoing identical
    processing.
    2) have a sample of the wave solder evaluated for contaminates and to
    establish the bench for future sample evaluations.

    Once again, your input and help will be much appreciated.

    Carol
    C. M. Spiers
    Director of Operations
    Interalia Inc.



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