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Corona Treater Dyne Level Verification Log

Log corona-treated film dyne readings before printing or lamination, so you can verify surface energy, catch treatment-side errors, and release only film that meets adhesion requirements.

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Built for: Flexible Packaging · Plastics Converting · Printing And Labeling · Film Extrusion

Overview

The Corona Treater Dyne Level Verification Log is an inspection record for confirming that corona-treated film has the surface energy needed for ink, coating, or adhesive adhesion before it moves into printing or lamination. It captures the inspection date and time, line or asset ID, film grade, downstream process, and the reference SOP so the reading can be tied to a specific run and procedure.

Use this template when surface treatment quality matters and a missed reading could lead to poor adhesion, print defects, or lamination failure. The form walks the inspector through treatment identification, including the roll or batch number, treated side, line speed, and treatment settings or power level, then records left, center, and right edge dyne readings to check uniformity across the web. It also provides space to document deficiencies, corrective action, and a retest after adjustment.

Do not use this as a substitute for process setup or maintenance records. If the issue is electrical, mechanical, or related to treater hardware condition, this log only documents the verification and the resulting release decision. It is also not a general lab test form for unrelated material properties. The value of the template is in making the surface-energy check repeatable, traceable, and easy to review when a job is held, adjusted, or released.

Standards & compliance context

  • This template supports ISO 9001:2015-style traceability, documented verification, and control of non-conforming output in a quality management system.
  • The record can be used as part of customer quality requirements for flexible packaging, printing, and converting operations where adhesion performance must be demonstrated.
  • If your site ties the log to chemical or process controls, align it with internal procedures and any applicable ANSI or industry consensus standards for surface treatment verification.
  • When the film is used in regulated packaging or food-contact workflows, keep the log aligned with your site’s FDA Food Code or customer-specific quality documentation practices as applicable.

General regulatory context for orientation only — verify current requirements with counsel or the relevant agency before relying on this template for compliance.

What's inside this template

Inspection Details

This section anchors the record to a specific run, so the reading can be traced back to the right line, material, and procedure.

  • Inspection date and time (critical · weight 3.0)
  • Production line or asset ID (critical · weight 3.0)
  • Film grade / material description (critical · weight 3.0)
  • Downstream process (weight 3.0)
  • Reference SOP or work instruction (weight 3.0)

Film and Treatment Identification

This section verifies that the correct roll and treated side were checked, which is essential for avoiding false passes and wrong-side errors.

  • Roll, lot, or batch number (critical · weight 4.0)
  • Treatment side identified and marked (critical · weight 4.0)
  • Corona treatment applied on correct side (critical · weight 4.0)
  • Line speed at time of treatment (weight 4.0)
  • Treatment settings or power level recorded (weight 4.0)

Dyne Readings and Surface Energy

This section captures the actual surface-energy results and shows whether the treatment is uniform enough for the downstream process.

  • Target dyne level for this job (critical · weight 6.0)
  • Dyne reading at left edge (critical · weight 8.0)
  • Dyne reading at center (critical · weight 8.0)
  • Dyne reading at right edge (critical · weight 8.0)
  • Readings are uniform across the web (critical · weight 5.0)
  • Surface energy meets minimum requirement for adhesion (critical · weight 5.0)

    Confirm the treated surface is at least 8-10 mN/m above the ink or adhesive surface tension target used for the job.

Condition, Deficiencies, and Corrective Action

This section documents what was wrong, what was done to fix it, and whether the fix was verified before release.

  • Any deficiency or non-conformance observed (weight 4.0)
  • Corrective action taken (weight 4.0)
  • Retest performed after adjustment (weight 4.0)
  • Retest dyne reading (weight 3.0)

Closeout and Attestation

This section records the final release decision and who approved it, creating a clear accountability trail.

  • Film released for printing or lamination (critical · weight 4.0)
  • Inspector signature (critical · weight 3.0)
  • Supervisor review required (weight 3.0)

How to use this template

  1. Enter the inspection date, time, production line or asset ID, film grade, downstream process, and the SOP or work instruction that defines the acceptance criteria.
  2. Record the roll, lot, or batch number, identify and mark the treated side, and note the line speed and treatment settings used during corona treatment.
  3. Measure dyne level at the left edge, center, and right edge of the web, then compare the readings to the target dyne level for the job and the minimum adhesion requirement.
  4. Document any deficiency or non-conformance, apply the corrective action, and repeat the test after the adjustment if the first reading is out of spec.
  5. Record the retest dyne reading, decide whether the film can be released for printing or lamination, and obtain the required inspector and supervisor signoff.

Best practices

  • Mark the treated side immediately after treatment so the wrong side is not tested or released by mistake.
  • Take readings at the same web locations on every roll to make results comparable across shifts and jobs.
  • Record the actual treatment settings or power level at the time of the run, not the nominal setup value from the recipe.
  • Use the same dyne test method and dwell time each time so the readings are consistent and defensible.
  • Flag any edge-to-center variation as a process issue, not just a pass/fail result, because non-uniform treatment often predicts downstream adhesion problems.
  • Photograph or attach evidence for any non-conformance when the film is held, especially if the roll will be reworked or retested later.
  • Do not release film after a failed reading until the retest confirms the corrected condition meets the minimum requirement.

What this template typically catches

Issues teams running this template most often surface in practice:

Treated side not identified, which leads to testing or printing the wrong surface.
Dyne readings taken at only one point on the web, missing edge-to-center variation.
Treatment power or line speed not recorded, making the run difficult to troubleshoot.
Readings below the target dyne level released without a documented corrective action or retest.
Film held for adhesion concerns but no non-conformance description was entered.
Supervisor review missing on jobs that require formal release authorization.
Retest performed after adjustment but the new reading was not captured in the log.

Common use cases

Packaging Quality Inspector
A quality inspector verifies corona-treated film before a flexographic print run to confirm the surface energy is high enough for ink anchorage. The log provides a clear release record if the roll is accepted or a documented hold if the readings are low.
Converting Line Lead
A line lead checks treated film after a speed change on the corona treater because adhesion complaints have increased on recent jobs. The template captures the settings change, the three-point readings, and the retest after the adjustment.
Lamination Process Technician
A technician confirms that the treated side of a film roll is correct before adhesive lamination begins. The form helps prevent a costly reversal error and records the minimum surface energy needed for bond performance.
Plant Quality Manager
A quality manager reviews dyne logs during a customer complaint investigation to trace whether the film met release criteria at the time of production. The structured record supports root-cause analysis and non-conformance review.

Frequently asked questions

What does this dyne verification log actually cover?

This template captures the inspection details, film and treatment identification, three-point dyne readings across the web, and any corrective action taken before release. It is designed for corona-treated film that will be printed, laminated, or otherwise bonded. The log also includes signoff fields so you can document who verified the result and whether supervisor review was required.

When should this log be used in production?

Use it after corona treatment and before downstream printing, coating, or lamination. It is especially useful at startup, after roll changes, after line adjustments, and whenever adhesion problems are suspected. If the job has a strict minimum surface energy requirement, this log should be completed before the material is released.

Who should complete the inspection?

A trained operator, quality inspector, or line lead should record the readings, with supervisor review when the template calls for escalation. The person taking the readings should know how to use the dyne test method consistently and how to identify the treated side of the film. If your site uses a formal quality system, assign the role in the SOP or work instruction referenced in the log.

Does this template help with compliance requirements?

Yes, it supports quality records and process verification expected under ISO 9001-style document control and traceability practices. It also helps demonstrate that the process was checked against internal specifications before release. While dyne testing itself is usually a quality control practice rather than a direct legal requirement, the record can support customer audits and non-conformance investigations.

What are the most common mistakes this log helps prevent?

Common failures include testing the wrong side of the film, recording only one reading instead of checking across the web, and releasing material without documenting a retest after adjustment. Another frequent issue is treating the line without recording the settings or power level, which makes troubleshooting difficult later. This log forces those details into one place.

How often should dyne readings be taken?

That depends on your process and customer specification, but many plants verify at startup, after treatment changes, after roll changes, and at defined intervals during the run. If the film is sensitive to speed, power, or material variation, more frequent checks are appropriate. The template includes a place to record the time and line conditions so you can align the cadence with your SOP.

Can this be customized for different films or downstream processes?

Yes, the target dyne level, acceptance criteria, and downstream process field can be tailored for specific film grades, inks, adhesives, or laminations. You can also add fields for test pen lot number, ambient conditions, or operator ID if your quality system requires it. The structure is flexible enough to support multiple product families without changing the core verification logic.

How does this compare with ad hoc notes or verbal release?

Ad hoc notes often miss the treatment side, the actual reading locations, or the retest result after adjustment. That makes it hard to prove the film was ready when it moved to the next process. A structured log creates a repeatable record that supports troubleshooting, traceability, and consistent release decisions.

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