3.2 Cleaning Methods & Fixtures
The effectiveness of board cleaning hinges on two elements working in harmony: the chemistry that dissolves residues and the fixturing that ensures fluids reach every hidden surface. Each method—aqueous spray, semi-aqueous, vapor degrease, or ultrasonic—has strengths tailored to specific geometries, soils, and sensitivities. Yet even the best chemistry fails without proper drainage angles, shielding for delicate parts, and drying that eliminates trapped moisture. Mastery comes from controlling measurable variables—time, temperature, turbulence, chemistry strength, and rinse purity—so that cleaning is no longer trial and error but a predictable, verifiable process.
3.2.1 Methods at a glance (what each is good for)
Inline vs batch: Inline is repeatable for volume; batch is flexible for NPI and diverse product sizes.
3.2.2 How to choose (simple matrix)
3.2.3 The 4T+M controls (what you actually set)
- Time: wash + rinse + dry durations; long enough to saturate crevices, not cook labels.
- Temperature: wash 45–65 °C typical; rinse 25–60 °C; vapor solvents per spec.
- Turbulence (impingement): nozzle pressure/angle, spray pattern, part rotation.
- Titration (chemistry strength): maintain by titration or refractometer; adjust for soil load.
- M—Megohm DI: final rinse ≥ 10–15 MΩ·cm (process target), stable and logged.
3.2.4 Spray-in-air setup (what “good” looks like)
- Nozzles: mix of fan + cone; aim across and into component fields; stagger heights to break shadowing.
- Pressure/flow: enough to flip beads from under BTC edges (don’t sandblast mask). Start around 1.5–3.0 bar and tune by coupon.
- Conveyor/rotation: slow enough for full wet-out; rotate or oscillate baskets for complex builds.
- Rinse train: at least 2–3 stages (counter-flow/cascade). Last stage is hot DI to cut spots.
- Breaks & drains: brief dwell after each stage so chemistry doesn’t drag forward.
Proof tools: glass test coupon with fiducials, hydrophobic marker tests, and UV tracer to check spray reach.
3.2.5 Ultrasonics (if you must)
- Limit to fixtures, shields, pallets, or very robust boards.
- Keep frequency ≥ 40 kHz and power low; short bursts.
- Do not use near MEMS mics/gyros, reed relays, quartz cans, or partially sealed components.
- Always rinse and dry thoroughly—ultrasonic loosened soils redeposit if not carried off.
3.2.6 Vapor degrease basics (modern, compliant units)
- Solvent choices: modern fluorinated / modified alcohol blends—check plastics, labels, and EHS.
- Zones: boil sump → rinse sump → freeboard; keep freeboard chiller cold to prevent loss.
- Process: pre-clean dip (optional) → vapor zone dwell until drip runs clear → slow lift to avoid streaks.
- Maintenance: water/sebum load skimming, solvent purity testing, leak checks, operator PPE.
3.2.7 Fixtures & shields (cleaning is 50% fixturing)
Goals: expose residues, prevent water traps, and protect “do-not-wet” parts.
- Angle for drainage: tilt 10–20° so trapped pockets empty; avoid perfectly flat panels.
- Open architecture: wire frames or perforated trays; no solid pans under boards.
- Hold-downs: minimal contact points; avoid masking solder joints; use PEEK/Delrin grips that survive chemistry/heat.
- Component covers: snap-on caps for relays, MEMS, trimmers, speakers, buzzers, displays, open frame coils, and any user-lubed mechanisms.
- Label guards: mask or shield labels/ink that aren’t wash-proof; spec wash-resistant labels at design time.
- Connector attitude: orient so housings don’t cup water; leave ports facing downstream.
- Board spacing: if racking multiples, keep ≥25–40 mm gaps for spray reach and airflow.
- Drain time: post-rinse tilt for 10–20 s before dryers.
3.2.8 Chemistry & rinse control (keep numbers, not guesses)
- Wash bath: titrate or refractive index each shift; top up deliberately—don’t chase foam.
- Filters & oil skimmers: change per delta-P or hours; soil-loaded baths redeposit grime.
- DI plant: log resistivity, TOC if available; sanitize on schedule.
- Carry-over watch: conductivity of intermediate rinses trending up = drag-out; add a stage or increase overflow.
3.2.9 Drying that really dries
Proof: weight before/after, IR camera for cold wet spots, or a quick “blot & UV” check on suspect areas.
3.2.10 Symptom → smallest reliable fix
3.2.11 Qualification & monitoring (keep it honest)
At NPI / chemistry change
- Run worst-case boards with witness coupons.
- Verify: IC (ion chromatography) species within limits, SIR on comb patterns after humidity bias, coat-wet if coating follows.
- Lock recipe IDs (temps, nozzle set, speeds, titration band, DI spec, dryer setpoints).
Routine
- Daily: titration/refract, DI resistivity, spray pattern check, filter ΔP, drain dwell verified.
- Weekly: nozzle inspection, bath skimming, DI log review.
- Monthly/Quarterly: IC on sentinel product, dryer audit (vacuum bake efficacy), EHS checks (solvent levels, emissions logs).
3.2.12 Pocket checklists
Setup (per product)
- Method chosen (aqueous / semi-aq / vapor); recipe ID loaded
- Fixtures angled; shields on sensitive parts; label guards in place
- Wash temp/chem in spec (titration logged); DI ≥ 10–15 MΩ·cm
- Nozzle pattern verified; conveyor/rotation set; drain dwell enabled
- Dryer mode set (vacuum if BTC-dense)
First article
- UV/marker coupon shows spray reach; no shadow stripes
- Boards emerge spot-free, dry to touch; no label/ink damage
- IC/SIR planned for first lot (if risk product)
If issues appear
- Fix rinse & drying before blaming chemistry
- Change one knob (impingement/time/temp/tilt) and re-inspect
- Capture before/after photos; note recipe rev comment