Transient Molecular Transfer During Vacuum Testing

Abstract

A common question in contamination budgeting involves the loss of collected volatiles during ambient I&T activity under vacuum and the resultant cross-contamination from outgassing. (1) How much of the material collected under ambient conditions evaporates under vacuum? (2) Why do pristine surfaces sometimes show increased molecular contamination after vacuum bakeout? (3) How much of the collected molecular contamination is transient (i.e. migratory) and how much is permanent? Measuring the transient deposition may be accomplished using a thermally passive QCM