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Subject:
From:
Bev Christian <[log in to unmask]>
Reply To:
TechNet E-Mail Forum <[log in to unmask]>, Bev Christian <[log in to unmask]>
Date:
Tue, 27 May 2014 21:26:45 -0400
Content-Type:
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text/plain (207 lines)
Well, I guess I have decided to wade in as well - with respect to using FTIR
(Fourier transform infrared spectroscopy).  Basically one is allowing
infrared light of different frequencies to interact with the changing dipole
moment as covalent bonds vibrate at infrared frequencies.

Let's first look at what this means for ionic solutions.  Salts with cations
like sodium, potassium, magnesium and calcium and anions like fluoride,
chloride and bromide are going to be completely disassociated in the water
and there will be no IR spectrum due to these salts. They are completely
ionic entities and there are no covalent bonds. 

What about sodium nitrate and sodium sulfate? Again the salts disassociate,
but in this case the anions are multi-atom entities that stay together (NO3-
and SO4-2).  Nitrate has four vibrations around 1040, 820, 1440 and 700 wave
numbers. I say "around", as the book I have only shows the values for the
solid salts and the values vary from salt to salt.  In solution only the
latter three vibrations are active in the infrared.  Many spectrometers use
NaCl cells and optics with the cutoff being 625 wave numbers, so for the
band at 700 it may be buried in the decreasing transparency as one
approaches 625 cm-1.  This doesn't give one a lot to work with.  If it is
mixed with organic molecules, which have a messy "fingerprint" region
(usually defined as below 1500 wave numbers), then hand me the aspirin.  

Multi-atom ions will have more active bands in solids because of crystal
effects splitting bands and making those active which are normally not
infrared active in the free gas or liquid phase.  However, this also can be
said for the other materials the salts may be mixed with.  What a mess. 

FTIR is NOT the technique to be looking for inorganic salts.

Now if one is looking for a common flux residue, coffee, Coke/Pepsi/Mountain
Dew, yes, we can tell the difference.  :)  

Regards,
Bev

-----Original Message-----
From: TechNet [mailto:[log in to unmask]] On Behalf Of Joe Russeau
Sent: Tuesday, May 27, 2014 2:41 PM
To: [log in to unmask]
Subject: Re: [TN] PCB Cleanliness Via Ion Chromatography Poll (informal)

Graham, Graham, Graham,

I about choked on my afternoon tea when I read your post.  I must disagree 
with you that IC is an unsuitable tool.  In fact, I would say it is highly 
suitable for evaluating bare board cleanliness.  And the items you point out

about bromide and false positives or false negatives are not necessarily a 
function of the tool, but perhaps more from improper use or inexperience 
using the tool or in understanding what it is that is being evaluated.  The 
gist of Rich's question (I think) is regarding what the industry experts 
consider as an appropriate metric for evaluating IC test results.  Rich 
correct me if I am wrong on that.

To add my 2 cents, I have said for many years now that there is no 
one-size-fits-all to this question.  Documents like IPC-5704 provide a 
general guideline for the evaluation of IC data on bare boards, but you have

to answer the question of how applicable that criteria is for your 
product(s).  If you have no clue of where to begin, then 5704 provides a 
remedial starting point.  As you begin to gather data, take the time to log 
it and evaluate it.  Hopefully, you are pulling data across multiple product

designs.  I tell clients all the time that every board has its own threshold

for how much residue it can tolerate.  So if you are only evaluating one 
board type, you can set a misleading standard for your other products.

Case in point, I had a client a couple of years back that had set an IC 
standard so low that none of their products could meet it.  When asked how 
they developed the standard, they told me that their competitor down the 
road used the same standard and they knew if their competitor could meet it,

so could they.  They neglected to take into account the material and process

differences they used compared to their competitor AND they never thought to

factor in their board supplier's process.  They went off assumptions.  We 
still do that in industry even today and make assumptions about what we 
think we know.  In my world, data is king.  So I would suggest that you 
test, re-test and test some more and look across multiple product lines.  I 
would look at different board laminates and different surface finishes and 
would tabulate the data that I collect.  Over time you should begin to see 
what the "typical" cleanliness picture is for your boards and then you will 
have a standard that is relevant to you.  Until then, I would recommend 
consulting the experts and utilize IPC documents as they are suppose to be 
derived from a consensus of industry experts that have knowledge and 
experience in a given area or discipline.

My 2 pennies.

Joe Russeau




----- Original Message ----- 
From: "Graham Naisbitt" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Tuesday, May 27, 2014 12:11 PM
Subject: Re: [TN] PCB Cleanliness Via Ion Chromatography Poll (informal)


Hi Richard

I was going to respond sooner but, being equally interested in the response,

thought I would wait to see what was said.

IMHO this is not a suitable test.

My reasoning being that the test is run by washing / "de-ionising" the 
eluent until it squeaks. Then heating it to 80DegC, and immersing the 
specimen / sample into the eluent for 1 hour.

Problem? The laminate closely resembles a sponge, it is hydrophilic and 
contains more ions than you could shake a stick at.

Result? False negatives?

Why? Br could well be leached out through the mask onto the surface..but Br 
is a requirement.

I have had several board fabricators asking for assistance on this matter as

they are struggling to get anything to pass... my answer has been: Use SIR 
sir.

It does not discriminate between ionic and non-ionic contamination, it 
simply examines changes to insulation resistance that might be pre-cursors 
of unwanted electro-chemical activity.

Use IC when you need to know what is present that is causing the problem..or

use FTIR?

Use Process Ionic Contamination Testing (PICT) to control the process. Fast,

simple, relatively inexpensive and effective.

Always at your service,

BR Graham Naisbitt


On 23 May 2014, at 14:27, Richard Kraszewski <[log in to unmask]>

wrote:

> I actually sent this out on May  16th, but never got a single response. 
> Hoping that was not due to lack of interest, but rather due to the TechNet

> being down. Hence, I think I'll try this one more time.
>
> I am  hoping to run an informal " min straw poll " here.
>
> Questions stated  are as follows:
>
>
> 1.       "Is your organization testing  incoming  PCB cleanliness  via 
> ion- chromatography?             Replies such as "YES" or "NO" will 
> suffice, but more detailed explanations are also acceptable.
>
>
>
> 2.       " If testing via IC, do you use IPC -5704 Table 4.1 limits or 
> other?                                                Replies such as " 
> IPC"  or "other"  will suffice, but more detailed explanations are also 
> acceptable.
>
> What's in  it for  you?   I will summarize and post the results after a 
> few days of replies.
>
> Rich  Kraszewski
> Senior Process Engineer
> Plexus
>
>
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