Prepreg plies
Fiber, resin content, backing, tack, batch and shelf/out-life are controlled.
Prepreg autoclave molding lays resin-impregnated reinforcement on a tool, seals it under vacuum and cures it in a pressure vessel with programmed temperature and external gas pressure. The route supports high-performance laminates when material life, lay-up, debulk, bag integrity and cure are tightly controlled.
Vacuum evacuates the bag while autoclave pressure consolidates the laminate during resin flow and cure. The complete pressure-temperature-vacuum history must match the qualified material and laminate thickness.
Verify prepreg condition, remaining life and frozen-storage history.
Cut kits and place each ply to the controlled orientation and boundary.
Compact interim stacks, install cauls and consumables, then seal the final bag.
Apply the qualified temperature, pressure and vacuum schedule.
Demold, trim, drill and verify the cured laminate and bonds.
Fiber, resin content, backing, tack, batch and shelf/out-life are controlled.
Honeycomb, foam, film adhesive and local details need compatible cure cycles.
Cauls, peel ply and release films shape surfaces and resin movement.
Breather, bag film, seals, ports, hoses and autoclave tooling.
A supplier claim is useful only when the process window is tied to the offered material, tooling, drawing revision and production batch.
| Stage | What must be controlled | Evidence to request |
|---|---|---|
| Material life | Storage, thaw, out-time, moisture and batch status. | Digital material-life log and freezer record. |
| Lay-up | Ply material, orientation, location, splices and foreign-object control. | Ply traveler, kit labels and inspection sign-off. |
| Bag & cure | Leak tightness plus pressure, vacuum and part temperature history. | Leak test and calibrated autoclave cure chart. |
| Release | Cure state, porosity, delamination, dimensions and machining. | Cure acceptance, NDT map and final inspection report. |
Likely cause: Air or volatile entrapment, poor vacuum, inadequate compaction or cure deviation.
Detection: Ultrasonic inspection, microscopy and cure-record review.
Likely cause: Poor drape, bridging, thermal movement or insufficient debulk.
Detection: In-process ply checks and final ultrasound/section analysis.
Likely cause: Contamination, trapped film, poor core fit or cure mismatch.
Detection: Ultrasound, tap testing where suitable and bondline inspection.
This guide uses the JEC process taxonomy, CAMX/ACMA/SAMPE review framework and process-specific material from industry associations, national research centers or government laboratories. Sources explain the process; they do not endorse listed suppliers.
Industry-level process taxonomy covering RTM, infusion, pultrusion, winding, fibre placement and additive manufacturing.
Peer-reviewed conference framework for manufacturing, processing, NDE and testing topics.
Bag stack, atmospheric compaction, air removal and prepreg or wet-lay-up routes.
Research evidence connecting cure processing, porosity risk and ultrasonic inspection.
Reviewed 16 August 2026. Verify current standards editions, material datasheets and project-specific acceptance requirements before award.
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Prepreg changes while warm and exposed. Uncontrolled cumulative out-time can alter tack, flow and cure response, so every thaw and lay-up interval must remain inside the qualified material specification.
Check calibrated part and tool temperatures, heat-up rate, dwell, pressure, vacuum continuity, cooling and any alarm or lag against the approved cure specification.
No. NASA research treats porosity as a critical cure defect; material handling, lay-up, bagging, vacuum and the cure cycle still determine quality and must be verified by process records and inspection.
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