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newSchoolWorks.com › VoTechWorks › Manufacturing & Marine › Fiberglass / Composites (boatbuilding) › Vacuum Infusion for Composite Boatbuilding › Lesson 7
MFG-COMP18-04 · Lesson 7 · 15 clock hours · lab

Integrated Infusion Build: Marine Hull Panel with Full Documentation

Objective. Each student will independently execute a complete vacuum infusion of a curved marine structural panel — from mold prep through post-cure and final quality inspection — producing a batch record, process log, and a written summary that meets industry traceability requirements.

⚠ Pending professional review

This lesson, its worked examples and its practice questions has not yet been verified by a licensed engineer or certified journey-level tradesperson or by a certification or approval body. It is a study draft and may contain errors. Do not use it as instructions for work on a job site or on live equipment. Always follow your instructor, your supervising professional, and current official references and regulations.

VoTechWorks program approval and accreditation are still in progress. Credentials are issued only by the certifying bodies named in each program, after their own exams.

Integrated Infusion Build: Marine Hull Panel with Full Documentation

This lab is your capstone infusion exercise. You will work alone — from bare mold to inspected part — and produce documentation that mirrors what a production composite shop submits with every structural marine panel. Accuracy in both the laminate and the paperwork is the professional standard the industry expects and what ACMA CCT and ABYC composite credentials test.

Why Documentation Matters in Marine Composites

A boat hull carries human lives. Regulatory bodies, surveyors, and insurance underwriters all expect that a builder can demonstrate — after the resin has cured and the mold is pulled — exactly what materials went in, at what temperature, mixed at what ratio, and inspected by whom. The production traveler, batch record, and process log are how that proof exists. In a certified shop, an incomplete batch record is treated the same as a nonconforming part: it stops production.

Your documentation package for this lab consists of three forms:

Mold Preparation and Stack Installation

Begin with a clean, structurally sound mold. Inspect for scratches or voids that could lock the part. Apply release agent per the manufacturer's system — paste wax, semi-permanent, or PVA — fully buffed and cured before any laminate touches the surface. Skipping or rushing release is the leading cause of part lockup.

Lay the reinforcement dry, following the instructor-provided laminate schedule. For this panel the schedule specifies biaxial fabric and woven roving over a structural core (PVC foam or balsa). Cut each ply precisely; overlapping biaxial layers at joints should meet the schedule's specified overlap width. Position the core, bevel or score the edges for resin flow if required. Install the infusion mesh or flow medium, spiral wrap feed line, and perimeter vacuum line, keeping feed and vacuum lines on opposite sides of the panel to ensure full cross-laminate flow.

Seal the bag, then pull vacuum. Hold the target vacuum level for a minimum 15 minutes with the pump isolated — watch the gauge for any rise. A passing integrity test shows less than the allowable pressure rise per your shop's standard (your instructor will state the acceptance criterion). Do not proceed to resin introduction until your instructor signs off on the vacuum test. This is the mandatory criterion; an infusion made without a passing test earns a zero regardless of part quality.

Safety Before You Mix

Vinyl ester resin with MEKP catalyst presents serious hazards.

Resin Mixing and Batch Record

Weigh resin and catalyst on a calibrated digital scale. Record lot numbers for resin, catalyst, and every reinforcement ply on the batch record before you open containers. Calculate the gel time for your room temperature using the resin technical data sheet. Your resin introduction must be planned so that you expect to complete flow before 80 percent of pot life has elapsed — this is the gel-time utilization criterion. Record ambient temperature and relative humidity at mix time; vinyl ester systems are sensitive to both.

Infusion Execution

With vacuum confirmed and instructor sign-off in hand, submerge your feed line, release the clamp, and watch the resin front advance. Photograph the flow front at three intervals (early, mid-panel, near completion) and timestamp each photo in your process log. Monitor vacuum level throughout — any significant drop indicates a bag breach; clamp the feed line and locate the leak before resin travels further. When resin reaches the vacuum line, pinch the line closed and maintain vacuum through gel. Log the time resin flow stopped and the time gel was visually confirmed.

Post-Cure Inspection and Nonconformance Reporting

After full cure, trim the panel with appropriate tooling. Perform a visual inspection under good lighting using a 10× loupe: look for dry spots, air bubbles, resin-starved zones, delamination at the core bond line, and pinholes. Follow with a tap test — use a tap-test mallet or coin and listen for the hollow thud that indicates a void or delamination compared to the solid ring of a well-consolidated area. Mark any anomaly with a pencil circle and record its location, size, and character on the nonconformance report form. Even a perfect part gets a completed NCR form showing no findings — that is what a traceable record looks like.

Writing the Process Summary

Your one-page summary must cover: material lot numbers, process conditions (temperature, humidity, gel-time utilization), a brief narrative of infusion events, inspection results, and your NCR conclusions. Write it so someone who was not present could reproduce the critical decisions you made. That is the standard the industry — and both credential bodies — expect.

Key terms9

Batch recordA completed form documenting the exact materials used in a composite layup, including lot numbers, mix ratios, quantities, and ambient conditions at the time of processing — the primary traceability document for a structural part.
Gel-time utilizationThe fraction of available pot life consumed during an infusion or layup operation, expressed as a percentage; industry practice limits use to 80 percent or less to ensure adequate flow before the resin becomes too viscous.
Vacuum integrity testA pressure-hold check performed after bagging but before resin introduction, in which the vacuum pump is isolated and the gauge is monitored for a set period to confirm the bag and fittings are leak-free.
Tap testA non-destructive inspection method in which a mallet, coin, or dedicated tool is tapped across a cured laminate surface; a hollow or dull sound compared to the surrounding area indicates a void, delamination, or disbond.
Nonconformance report (NCR)A formal record documenting any deviation from specification found during inspection — including location, size, and nature of the defect — used to decide whether a part is accepted, repaired, or rejected.
Production travelerA set of documents that travels with a part through the manufacturing process, collecting batch records, inspection sign-offs, and process notes so the complete history of the part is captured and auditable.
MEKP (methyl ethyl ketone peroxide)The organic peroxide catalyst used to initiate cure in polyester and vinyl ester resin systems; classified as an oxidizer and a serious eye and skin hazard requiring chemical-splash goggles and chemical-resistant gloves.
Flow medium (infusion mesh)A highly porous, open-weave material placed on top of the dry laminate stack in vacuum infusion to distribute resin rapidly across the surface before it penetrates through the reinforcement layers.
Biaxial fabricA fiberglass reinforcement with fibers oriented in two directions (commonly ±45° or 0°/90°), stitched together without crimp, providing balanced in-plane strength suited to marine structural panels.

Worked examples4

1. You are mixing vinyl ester resin for the infusion panel. The laminate schedule calls for 1,200 g of resin. The technical data sheet specifies 1.5% MEKP by weight. How many grams of MEKP do you need, and what do you record on the batch record?
  1. Identify the resin mass: 1,200 g.
  2. Convert the percentage to a decimal: 1.5% = 0.015.
  3. Multiply resin mass by the decimal: 1,200 g × 0.015 = 18 g of MEKP.
  4. Record on the batch record: resin lot number, resin mass = 1,200 g; MEKP lot number, MEKP mass = 18 g; mix ratio = 1.5% by weight; date/time; operator name; ambient temperature and humidity.
Answer: 18 g of MEKP. The batch record must show both lot numbers, both masses, the calculated ratio (1.5% w/w), and the ambient conditions at mix time.
2. At your shop temperature the resin technical data sheet shows a pot life of 25 minutes. The gel-time utilization limit is 80%. What is the latest time (in minutes from mixing) at which infusion flow must be complete, and how much working time margin does that leave?
  1. Multiply pot life by the utilization limit: 25 min × 0.80 = 20 minutes.
  2. This means resin flow must reach the vacuum line by 20 minutes after mixing.
  3. Remaining margin before actual gel: 25 min − 20 min = 5 minutes of buffer.
Answer: Flow must be complete by 20 minutes after mixing, leaving a 5-minute safety margin before the resin reaches its gel point.
3. During your vacuum integrity test, you isolate the pump with the gauge reading 25 in-Hg. After 15 minutes the gauge reads 23.5 in-Hg. Your shop standard allows a maximum rise of 1 in-Hg over 15 minutes. Does the bag pass or fail, and what must you do next?
  1. Calculate the pressure rise: 25 in-Hg − 23.5 in-Hg = 1.5 in-Hg rise (vacuum dropped, so absolute pressure increased by 1.5 in-Hg).
  2. Compare to the acceptance criterion: 1.5 in-Hg rise exceeds the 1 in-Hg limit.
  3. The bag fails the integrity test.
  4. Reconnect the pump, restore vacuum, and use soapy water or leak-detection film to locate and seal the leak, then repeat the 15-minute hold test before calling for instructor sign-off.
Answer: The bag fails — 1.5 in-Hg exceeds the 1 in-Hg allowable rise. You must find and seal the leak, then repeat the integrity test until it passes before proceeding.
4. Your tap-test inspection reveals a circular area that sounds hollow. You measure it as roughly 9 mm in diameter. The rubric states that no dry spots greater than 6 mm are acceptable. How do you handle this on your documentation?
  1. Confirm the measurement: 9 mm > 6 mm threshold, so this is a nonconforming condition.
  2. Mark the location on the part with a pencil circle.
  3. Complete the nonconformance report: record the location (e.g., distance from panel edge), measured size (9 mm diameter), character (hollow tap response, suspected dry spot or void), and your name and date.
  4. The panel does not pass criterion 3 of the rubric; note this in your written process summary and state that the NCR has been filed.
  5. Do not alter or sand the area before the instructor reviews it.
Answer: The 9 mm anomaly exceeds the 6 mm limit. Complete the NCR fully, mark the location on the part, note the nonconformance in your process summary, and present the part to the instructor without modification.

The math in this lesson2

Learners compute MEKP for 1,200 g of resin and the latest infusion time at 80 percent of pot life.
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Brush up in the math halls at newSchoolWorks.com:
In class: Individual mold preparation and stack installation: student applies release, lays up the specified biaxial and core laminate schedule (instructor-provided drawing), installs infusion consumables, and achieves a passing vacuum-integrity test before calling for instructor sign-off to proceed. · Solo infusion execution: student mixes resin batch, records all batch-record fields, executes infusion from resin introduction to vacuum-line shutoff, photographs infusion front at three intervals, and timestamps each event. · Post-cure quality inspection and written summary: after cure, student trims part, performs visual inspection and tap test, records any anomalies on a nonconformance report, and writes a one-page process summary covering material lot numbers, process variables, observations, and inspection results — modeled on production traveler documentation used in the marine composites industry.
Materials: Curved mold (instructor-provided, representing a hull section), specified fiberglass reinforcement (biaxial and woven roving per laminate schedule), structural core material (PVC foam or balsa), infusion vinyl ester resin, MEKP, full infusion consumable set, digital scale, thermometer, hygrometer, batch-record and process-log forms, nonconformance report form, tap-test mallet, 10× loupe, PPE, trimming tools (pneumatic cutter or oscillating saw, hearing protection)
Check: Instructor evaluates finished panel against a five-criterion rubric: (1) vacuum integrity achieved before infusion, (2) batch record complete and gel-time utilization ≤ 80%, (3) no dry spots > 6 mm on visual and tap-test inspection, (4) process log fully completed with timestamps and photos, (5) written summary includes all required fields. Pass = 4 of 5 criteria met at acceptable standard; criterion 1 (vacuum integrity) is mandatory — a part infused without a passing integrity test scores zero. ACMA CCT and ABYC composite domain competencies mapped here.

Practice check8

Answer each question, then check it. Nothing is recorded; this is your own practice.

ACMA CCT — Vacuum Infusion Process
1. According to this lesson, what must happen before a student is permitted to introduce resin into the vacuum bag?
ACMA CCT — Resin Chemistry and Mixing
2. A student mixes 800 g of vinyl ester resin with 1.5% MEKP by weight. What mass of MEKP is needed?
ABYC Composite Boat Builder — Safety
3. Which personal protective equipment is specifically required when mixing and handling MEKP-catalyzed vinyl ester resin, beyond standard safety glasses?
ACMA CCT — Process Control
4. The gel-time utilization limit for an infusion is 80%. If the resin pot life at room temperature is 30 minutes, by how many minutes after mixing must the infusion flow be complete?
ABYC Composite Boat Builder — Quality Inspection
5. During a tap test, a section of the cured panel produces a noticeably hollow sound compared to surrounding areas. What is the most likely explanation?
ACMA CCT — Vacuum Infusion Process
6. A student's vacuum integrity test shows a 0.8 in-Hg rise over 15 minutes against a shop standard allowing a maximum 1 in-Hg rise. What is the correct action?
ABYC Composite Boat Builder — Documentation and Traceability
7. Which fields are required on a composite batch record to meet industry traceability requirements as described in this lesson?
ACMA CCT — Quality Assurance and Documentation
8. A student discovers a circular anomaly 9 mm in diameter that sounds hollow on tap testing. The rubric criterion states no dry spots greater than 6 mm are acceptable. What is the correct professional response before presenting the part to the instructor?
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