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Environmental chamber cleanliness is critical: the right cleaning protocol can eliminate false failures.


A quality or reliability test is only as good or accurate as the test equipment used. When performing humidity testing, results can only be accurate indicators of product performance if the interior of the testing chamber is free of contaminants. Having an effective cleaning protocol to control the testing environment is crucial to achieve valuable results. Take care in choosing a cleaner for the interior of a chamber, because many cleaners have the potential to introduce contamination into the chamber. When contaminants in a chamber deposit on boards during environmental testing, these contaminants will interact with the moisture introduced through humidity to potentially cause false failures for clean boards.

[TEXT NOT REPRODUCIBLE IN ASCII ASCII or American Standard Code for Information Interchange, a set of codes used to represent letters, numbers, a few symbols, and control characters. Originally designed for teletype operations, it has found wide application in computers. ]

In a recent investigation, assemblies were failing 100% of the time during ESS (1) (Electronic Switching System) A large-scale computer from Lucent used to route telephone calls in a telephone company office. The 5ESS is a Class 5 central office switch, and the 4ESS is a Class 4 tandem office switch.  testing on three consecutive attempts. This was a new ESS testing chamber, identical to a chamber from another facility. The only difference was that the operating environment In computing, an operating environment is the environment in which users run programs, whether in a command line interface, such as in MS-DOS or the Unix shell, or in a graphical user interface, such as in the Macintosh operating system.  outside the chamber was not climate-controlled; the older chamber was in a climate-controlled environment and did not present a significant amount of failures. We received boards from the failed humidity tests along with untested boards to perform ion chromatography Ion-exchange chromatography (or ion chromatography) is a process that allows the separation of ions and polar molecules based on the charge properties of the molecules.  analysis and determine the precise levels of ionic i·on·ic
adj.
Of, containing, or involving an ion or ions.



ionic

pertaining to an ion or ions.


ionic medication
iontophoresis.
 contamination. Current ROSE (resistivity resistivity

Electrical resistance of a conductor of unit cross-sectional area and unit length. The resistivity of a conductor depends on its composition and its temperature.
 of solvent extract) testing showed passing results, and very little difference between groups.

[ILLUSTRATION OMITTED]

Using ion chromatography analysis, the boards showed acceptably low levels of all detected residues prior to humidity testing. These low-residue levels pose little or no risk of electrochemical electrochemical /elec·tro·chem·i·cal/ (-kem´i-k'l) pertaining to interaction or interconversion of chemical and electrical energies.

e·lec·tro·chem·i·cal
adj.
 or electromigration problems in a biased, high humidity environment. The 30 assemblies that underwent high humidity (90% RH) testing in a non-condensing biased environment all failed due to electromigration. Ion chromatography analysis of these boards showed very high chloride and sulfate sulfate, chemical compound containing the sulfate (SO4) radical. Sulfates are salts or esters of sulfuric acid, H2SO4, formed by replacing one or both of the hydrogens with a metal (e.g., sodium) or a radical (e.g., ammonium or ethyl).  levels of up to eight times greater than the levels found prior to high humidity exposure.

A second set of samples was submitted for testing: alcohol wiping samples from a 1 i[n.sup.2] area (for 30 sec. of contact time) of the chamber door, walls, ceiling and floor. A second type of sample was a 4 i[n.sup.2] piece of aluminum foil Noun 1. aluminum foil - foil made of aluminum
aluminium foil, tin foil

foil - a piece of thin and flexible sheet metal; "the photographic film was wrapped in foil"
 that had been placed in the chamber in the same manner the boards were placed, and was exposed to the high humidity for 24 hours Adv. 1. for 24 hours - without stopping; "she worked around the clock"
around the clock, round the clock
. After collecting the wiping samples, running the chamber and extracting samples of the deionized de·i·on·ize  
tr.v. de·i·on·ized, de·i·on·iz·ing, de·i·on·iz·es
To remove ions from (a solution) using an ion-exchange process.



de·i
 feed water and steam reservoir, all these samples were sent along with a control sample of each.

The analysis of the second set of samples (foil and alcohol wiping samples) showed that a high contamination event had occurred, but the DI feed water and the steam reservoir showed low levels of contamination. The contamination was high in chloride, sulfate and amines amines (mēnz´),
n.pl organic compounds that contain nitrogen.
. The amounts of chloride, sulfate and amines were much higher before the cleaning of the chamber, and after the chamber cleaning, no failures occurred on ionically clean assemblies (Table 1).

[TEXT NOT REPRODUCIBLE IN ASCII]

Based on these findings, we suggested that the customer clean the chamber first by scrubbing the inside with a Scotch Brite pad with 10 M[OMEGA 1. (programming) Omega - A prototype-based object-oriented language from Austria.

["Type-Safe Object-Oriented Programming with Prototypes - The Concept of Omega", G. Blaschek, Structured Programming 12:217-225, 1991].
2.
] deionized water Deionized water (DI water or de-ionized water; also spelled deionised water, see spelling differences) is water that lacks ions, such as cations from sodium, calcium, iron, copper and anions such as chloride and bromide. , working from top to bottom. The chamber should be scrubbed three times, then wiped with DI water and a lint-free cloth over all surfaces including the vents and air inlet inlet /in·let/ (-let) a means or route of entrance.

pelvic inlet  the upper limit of the pelvic cavity.

thoracic inlet  the elliptical opening at the summit of the thorax.
 opening. Next, the chamber should be wiped three times with IPA IPA - International Phonetic Alphabet  using critical contact polyester wipes.

Apparently, the equipment fabricator fab·ri·cate  
tr.v. fab·ri·cat·ed, fab·ri·cat·ing, fab·ri·cates
1. To make; create.

2. To construct by combining or assembling diverse, typically standardized parts:
 had used a stainless steel stainless steel: see steel.
stainless steel

Any of a family of alloy steels usually containing 10–30% chromium. The presence of chromium, together with low carbon content, gives remarkable resistance to corrosion and heat.
 cleaner to clean the chamber before shipment, and this residue was introducing the harmful chloride, sulfate and amine amine (əmēn`, ăm`ēn): see under amino group.
amine

Any of a class of nitrogen-containing organic compounds derived, either in principle or in practice, from ammonia (NH3).
 residues that caused the humidity tests to fail. The presence of these contaminants caused the ESS test results to be an inaccurate gauge of product performance. After following our recommended cleaning protocol, this customer saw results that were much more accurate predictors of product cleanliness Cleanliness
See also Orderliness.

Cleverness (See CUNNING.)

Berchta

unkempt herself, demands cleanliness from others, especially children. [Ger. Folklore: Leach, 137]

cat

continually “washes” itself.
 and reliability. The first two groups after cleaning showed 0% failures with low ionic residue problems. We conducted ongoing monitoring of this chamber for several months, and the contamination problem was alleviated. This case exemplifies how important it is to maintain the cleanliness of test equipment to achieve meaningful results upon which quality decisions can be made.
TABLE 1: Contaminant levels before and after chamber cleaning.

all values are in [micro]g/i[n.sup.2]        Ion Chromatography
unless otherwise noted

Sample Description                      Cl *    Br *  S[O.sub.4.sup.2-]

Assembly prior to ESS biased humidity
testing

Sample area U5                          1.24    1.32        0.26

Assembly after ESS biased humidity
testing

Sample area U5                          10.27   6.39        7.59

Wiping samples of 1 i[n.sup.2] areas
(30 sec) prior to cleaning

 Door area                              15.26    0          9.36

 Right wall area                        19.39    0          8.54

 Left wall area                         14.24    0          8.11

 Back wall area                         15.61    0          9.06

 Ceiling area                           19.22    0         10.21

 Floor area                             27.36    0         13.26

 Control wiping (unused)                 0.23    0          0.43

 Foil exposed to ESS humidity chamber    8.95    0          5.39
 24 hours

 Control foil sample prior to            0.06    0          0.09
 exposure (unused)

Wiping samples of 1 in2 areas (30
seconds) After Cleaning with DI water
and Scotch Brite (green pad)

  Door area                              0.27    0            0

  Right wall area                        0.37    0            0

  Left wall area                         0.42    0            0

  Back wall area                         0.61    0            0

  Ceiling area                           0.24    0            0

  Floor area                             0.89    0            0

  Control wiping (unused)                0.19    0            0

  Foil exposed to ESS humidity           0.64    0          0.08
  chamber 24 hours

  Control foil sample prior to           0.03    0          0.04
  exposure (unused)

DI feed water                          .02 ppm   0         .01 ppm

DI water from steam resevoir           .03 ppm   0         .03 ppm

all values are in [micro]g/i[n.sup.2]         Ion Chromatography
unless otherwise noted

Sample Description                      WOA     Na+    N[H.sub.4]+   K+

Assembly prior to ESS biased humidity
testing

Sample area U5                         12.36   0.26       0.89      0.11

Assembly after ESS biased humidity
testing

Sample area U5                         11.08   0.34       5.69      0.08

Wiping samples of 1 i[n.sup.2] areas
(30 sec) prior to cleaning

 Door area                               0       0        8.59       0

 Right wall area                         0       0        9.68       0

 Left wall area                          0       0        8.77       0

 Back wall area                          0       0        9.36       0

 Ceiling area                            0       0        9.18       0

 Floor area                              0       0       10.07      0

 Control wiping (unused)                 0       0          0        0

 Foil exposed to ESS humidity chamber    0       0        4.74       0
 24 hours

 Control foil sample prior to            0       0          0        0
 exposure (unused)

Wiping samples of 1 in2 areas (30
seconds) After Cleaning with DI water
and Scotch Brite (green pad)

  Door area                              0       0        0.11       0

  Right wall area                        0       0        0.06       0

  Left wall area                         0       0        0.13       0

  Back wall area                         0       0        0.05       0

  Ceiling area                           0       0        0.18       0

  Floor area                             0       0        0.22       0

  Control wiping (unused)                0       0          0        0

  Foil exposed to ESS humidity           0       0        0.13       0
  chamber 24 hours

  Control foil sample prior to           0       0          0        0
  exposure (unused)

DI feed water                            0    .01 ppm       0        0

DI water from steam resevoir             0    .02 ppm       0        0


Terry Munson is with Foresite Inc. (residues.com); tm_foresite@residues.com
COPYRIGHT 2005 UP Media Group, Inc.
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2005, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Title Annotation:Process Doctor
Author:Munson, Terry
Publication:Circuits Assembly
Date:Mar 1, 2005
Words:1230
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