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Seal-area contamination control

How Do You Keep Product Out of Sachet Seals?

Keep product out of sachet seals by controlling dose volume, cut-off, drop path, settling time, headspace, film movement and the interval before the cross jaws close.

Sachet forming and sealing machine used to explain product contamination at the seal area

The direct answer

Product is kept out of the cross seal by giving the dose a controlled path and enough usable pack volume to finish moving before the jaws close. The solution may involve dose, nozzle or auger timing, headspace, cut-off, dust control, film motion and product-feed stability.

Seal settings cannot compensate reliably for product trapped between the film layers. Begin by identifying when contamination appears and what product mechanism caused it, then confirm the corrected process with an agreed pack-integrity method and retained samples.

Why does product enter the sachet seal area?

Common causes include overfill, insufficient headspace, late product fall, liquid dripping, paste stringing, foam rise, powder dust, particle bounce and movement of the pack before the dose has settled.

The cause may be continuous or linked to a transient such as refill, stop, restart or temperature change. Inspect sequential packs and the machine timing rather than treating every contaminated seal as a film or heater fault.

How do headspace and fill timing reduce contamination?

Headspace creates a clear zone between the product and the cross seal, while timing allows the dose to enter and settle before the film advances or the jaws close.

More headspace can improve margin but increases pack length and material use. More settling time can reduce cycle output. The optimum must be proven with the most demanding product/dose/pack combination, not chosen from an empty-film test.

What should be checked when contamination appears after refill?

Check whether refill changes product pressure, aeration, bulk density, hopper level, agitation, feeder flow or the timing of the next dose.

Liquids may entrain air or surge; powders may become aerated or compacted; granules may avalanche. Retain packs immediately before, during and after refill and record the relevant level or feeder state. Later stable packs cannot explain the transient.

How do powder dust and liquid drips need different controls?

Powder dust is controlled through product flow, drop containment, air movement and film/jaw cleanliness, while liquid drips require valve and nozzle closure, pressure control and enough time for cut-off.

A paste tail may need a different closure or suck-back action, and granules may need a wider path or reduced bounce. The acceptance test should use product-specific observations and not one generic statement that the seal “looks good”.

Why can increasing seal temperature hide the real problem?

Higher temperature may temporarily bond around light contamination, but it does not remove product, restore film-to-film contact or correct a dosing and timing fault.

Excessive heat can reduce process margin, distort film, increase residue or create inconsistent seals after a stop. Return to the approved film and seal window, clean and inspect the jaws, then correct the product path before revalidating the seal.

Seal-contamination fault table

Evidence patternLikely process areaNext controlled check
Every packPack volume, fill timing or constant cut-off problemReduce to known baseline and observe dose-to-jaw sequence
Only after refillFeed pressure, aeration, compaction or surgeRecord levels and sequential packs around refill
One lane onlyLane-specific nozzle, auger, chute or seal alignmentKeep lane identity and compare neighbouring lanes
Only at higher speedInsufficient settle/cut-off time or unstable film motionCompare accepted packs across controlled setpoints
After a pauseDrip, relaxation, settling or first-dose responseInspect first packs and stopped product position

Acceptance and enquiry inputs

  • Product condition, dose, pack volume and required headspace.
  • Film structure and the agreed seal-process window.
  • Nozzle, auger or chute geometry and product feed conditions.
  • Samples from start-up, stable running, refill, pause, restart and upper intended output.
  • Agreed visual, strength or leak-test method and pass criteria.
  • Lane identification, reject response and retained-sample plan.

For food applications, the pack owner should use packaging suitable for the intended food-contact use and retain the appropriate supporting evidence. Machinery trials establish runnability and seal-process evidence but do not replace material compliance or shelf-life assessment. Read Food Standards Agency packaging guidance.

Related answers

Continue with the next connected decision

Review film and sealing

Connect laminate construction, sealant layer, web drawing and trial method to the required pack-integrity result.

Troubleshoot sachet faults

Use a controlled fault record to separate product-path, film, jaw, timing, temperature and pressure causes.

Control foaming liquids

Reduce product entering the seal by addressing aeration, fill motion, headspace and settling before closure.

Control difficult powders

Reduce dust at the jaws by controlling feed, dosing, film movement and the condition of the seal faces.

Apply the answer to your production case

Send the product, sachet and operating conditions for review

Provide representative product, dose range, sachet drawing, film or artwork data, target accepted output and the site or line constraints that affect the answer. Lancing Ltd can then identify the machine route and evidence still required before quotation.

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