What’s past isn’t prologue: A better understanding of contamination is needed.

Process Doctor The definition of board cleanliness is changing. It is not just the general visual or normalized number for the whole board we have understood it to be. Historically, it has been defined by total board cleanliness requirements of the military and IPC specifications of the 1970s. Board cleanliness has not evolved as assembly, interconnect, flux and component packaging have evolved. The difference between the historical definition of cleanliness and what is needed today is a direct understanding of what localized contamination is around critical sensitive circuits.

Historically, board cleanliness was:


ImageWhat has changed that limits the effectiveness of this type of cleanliness testing? The primary changes can be answered by looking at four key areas:


Localized cleanliness. To understand an assembly’s cleanliness requires a look at the effect of each process and nearby process, especially in critical circuit areas. The cleanliness of individual components, and spacing between leads on QFP, DIPS, QFN and connector leads, are areas for residues to impact performance. No-clean manufacturing techniques using selective wave techniques, dirty components, dirty bare boards, high levels of contamination on innerlayers, hand solder residues, residues nearby and areas around brush cleaning all rely on the understanding that these residues are benign.

Board cleanliness must represent the amount of residues detected in critical areas that correlates to electrical performance in the field and environmental stress screening. This approach as a process control technique must permit the assembler the opportunity to have failures (dirty boards) optimize the process, and then maintain this cleanliness level and not have field failures from qualified processes.

Terry Munson is with Foresite Inc. (residues.com); tm_foresite@residues.com. His column appears monthly.

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