| HS Code | 672782 |
| Product Name | M-640 General Purpose Mineral Oil Defoamer |
| Appearance | Milky white to off-white liquid |
| Chemical Type | Mineral oil-based defoamer |
| Active Content | 100% active defoamer compound |
| Specific Gravity | 0.85 - 0.95 |
| Viscosity | 100 - 300 cP at 25°C |
| Ph | 5.0 - 8.0 |
| Flash Point | >150°C |
| Solubility | Dispersible in water |
| Foam Suppression | Fast knockdown and sustained foam control |
| Compatibility | Compatible with most nonionic and anionic systems |
| Recommended Dosage | 0.05% - 0.5% by weight |
As an accredited M-640 General Purpose Mineral Oil Defoamer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Available in 5-gallon pails: M-640 General Purpose Mineral Oil Defoamer, a concentrated liquid for effective foam control. |
| Container Loading (20′ FCL) | M-640 mineral oil defoamer is loaded in a 20' FCL as palletized drums/IBCs, securely fastened, labeled, and documented for safe transport. |
| Shipping | M-640 General Purpose Mineral Oil Defoamer ships as a non-hazardous industrial chemical. It is not regulated by DOT, IATA, or IMDG for ground, air, or ocean transport. Standard packaging in sealed containers, protected from extreme heat/freezing. Ensure proper labeling and upright handling to prevent spills. |
| Storage | Store M-640 General Purpose Mineral Oil Defoamer in its original, tightly closed container in a cool, dry, well-ventilated area. Keep away from heat, sparks, open flames, and strong oxidizers. Protect from direct sunlight, moisture, and freezing temperatures. Ensure secondary containment nearby, and store separately from incompatible substances. always follow label and SDS instructions. |
| Shelf Life | M-640 General Purpose Mineral Oil Defoamer has a shelf life of 24 months when stored in original, unopened containers. |
In waterborne architectural coating production, M-640 General Purpose Mineral Oil Defoamer is introduced at two separate dosing points because the foaming mechanism in the pigment-grind phase differs from that in the letdown phase. During high-speed dispersion of titanium dioxide and extender pigments in a Cowles-blade disperser operating at 18–25 m/s tip speed, surfactant-stabilized microfoam with mean bubble diameters in the 10–50 µm range is generated; in the subsequent letdown phase, low-shear incorporation of latex binder and rheology modifiers entrains macrofoam with bubble diameters above 100 µm. The total defoamer addition for vinyl-acrylic and acrylic interior and exterior architectural formulations ranges from 0.10 to 0.50 wt% on total batch weight. The split between grind and letdown is not arbitrary: high-PVC flat paints receive 40–60% of the total dose in the pigment grind because the pigment paste contains high-foaming dispersant loads; semi-gloss and satin bases receive only 10–20% in the grind and the balance in the letdown to avoid surface defects at 60° gloss values above 35 GU measured under ISO 2813:2014. Production-scale mixing records indicate that addition must occur before the dispersion reaches 55 °C; at temperatures above 60 °C, the mineral oil carrier can migrate to the air–liquid interface too rapidly and create cratering and intercoat adhesion loss under ASTM D3359 tape pull tests. Foam control is evaluated with ASTM D3519 blender foam tests and by drawdown appearance, while VOC compliance for the final paint is determined under EPA Method 24 or ASTM D3960, with finished goods limits aligned to Directive 2004/42/EC. The table below represents typical starting-point ranges reported from production-scale batches for three paint categories.
| Paint category | Pigment volume concentration | Defoamer addition | Grind/letdown split | Typical defect threshold |
| Flat interior ceiling and wall paint | 75–85% PVC | 0.40–0.70 wt% | 50/50 | Scrub loss observed above 0.8 wt% under ISO 11998; cratering rare |
| Eggshell and satin wall paint | 30–45% PVC | 0.20–0.40 wt% | 30/70 | Visible fisheyes appear above 0.5 wt% on knife-drawn cards |
| Semi-gloss and gloss tint bases | 20–28% PVC | 0.10–0.25 wt% | 20/80 | 60° gloss reduction and craters occur above 0.3 wt% |
Finished products from this application class include interior flat, ceiling, eggshell, satin, and semi-gloss latex paints, primer-sealers, exterior flat and satin paints, and tint bases. The upper dose boundary in waterborne architectural systems is constrained by surface defect generation rather than foaming persistence; mineral oil carrier entrainment at high dose can reduce intercoat adhesion and compromise scrub resistance under ISO 11998.
Water-based flexographic ink flows through enclosed doctor blade chambers at line speeds between 0.5 m/s and 1.5 m/s, and the resulting turbulence combined with return to an open holding tank builds a mixed foam layer at the surface. Entrained microfoam transferred to anilox cells below 8 cm³/m² cell volume produces print mottling and skip marks on kraft and mottled white-top liner. M-640 is introduced in the final letdown after pigment dispersion and before final amine pH adjustment, at 0.20–0.60 wt% based on finished ink mass. Heavily pigmented carbon black or cyan inks may require 0.70–0.80 wt%, but only after drawdown tests confirm absence of drainage holes on a 200-lin/cm anilox hand proofer. The production process includes predispersion of organic pigments in a bead mill to a grind gauge below 5 µm under ISO 1524 or ASTM D1316, letdown under a high-torque low-speed stirrer at 200–500 rpm, and viscosity adjustment to 18–30 s in a DIN 4 mm cup under ISO 2431. Compliance for corrugated packaging inks includes heavy-metal limits under CONEG/TPCH and the packaging waste directive 94/62/EC, while indirect food contact work must follow EuPIA low-migration guidance and, for certain applications, national food packaging regulations. Terminal finished products include water-based flexo inks for corrugated preprint liner, paper sacks, folding cartons, trays, and wrappers, including low-odor and low-migration grades for dry food packaging. The operational boundary is that final pH above 9.4 can reduce droplet coalescence performance; the defoamer is therefore added before amine neutralization, not after the batch has been brought to high pH.
In vinyl acetate–ethylene emulsion polymerization, M-640 is excluded from the initial reactor charge because free mineral oil droplets present during micellar nucleation can act as hydrophobic sinks that alter monomer diffusion and final particle size distribution. The product is introduced after residual monomer stripping and cooling, when the dispersion temperature is at or below 45 °C. Typical addition rates range from 0.05 wt% to 0.30 wt% on total wet dispersion weight, with high-solids vinyl acetate–ethylene grades above 60% solids usually requiring 0.15–0.25 wt% because surfactant and protective colloid loads generate persistent surface foam. The post-polymerization letdown vessel is normally a stainless steel tank with an anchor or low-shear pitched-blade stirrer held below 60 rpm; high-shear post-addition is avoided because it can re-emulsify the defoamer droplets and reduce knockdown efficiency. Solids are checked after addition under ISO 3251, Brookfield viscosity is determined under ASTM D2196, and residual vinyl acetate monomer is monitored by GC-FID to below plant specification. Finished dispersions are used in water-based adhesives, paper and nonwoven binders, carpet backing compounds, footwear adhesives, and laminate adhesives where FDA 21 CFR 175.105 indirect food contact compliance is often required for packaging laminations. REACH and local VOC requirements apply to the commercial dispersion. The main operational delimiter is the addition window; dosing at temperatures above 55 °C or directly into the reactor before free radical termination can cause destabilized pre-coagulum and filter plugging on 100 µm discharge filters.
Paper coating colour defoaming is evaluated not by foam height alone; blade-run microfoam, entrapped air pockets, and coating surface streak count are the operational acceptance criteria on an off-machine coater. In the coating kitchen, mineral pigment slurry is dispersed with polymeric dispersant and then combined with styrene-butadiene or styrene-acrylate latex and co-binder starch at total solids of 55–68%. M-640 is added after latex letdown at 0.03–0.20 wt% based on dry pigment weight, because addition before pigment dispersion reduces its efficiency and the product may adsorb onto filler surfaces. On blade coaters running at 800–1,500 m/min, the coating colour experiences high shear at the blade tip, and microfoam smaller than 30 µm can survive low-shear pumping and create skip coating or streaks. Dosing into the run tank at the point of return flow, followed by one to two minutes of gentle circulation, is preferred over dosing directly into the blade coater supply line. Production quality is controlled by deaeration tests, coating colour viscosity under ISO 2884, and finished surface roughness under ISO 8791-4 or Parker PrintSurf. Compliance for food-contact board and packaging grades is documented under Framework Regulation (EC) No 1935/2004 and, where applicable, BfR Recommendation XXXVI for paper and board; REACH registration covers the defoamer component inventory. Final products include coated fine paper, lightweight coated magazine paper, folding boxboard, white-top kraftliner, and thermal paper base. Reported batch records show that exceeding 0.25 wt% on dry pigment can depress sheet gloss and sheet gloss uniformity; published data for specific high-speed blade configurations is limited, so verification on a pilot coater is standard before committing to high-dose campaigns.
In municipal and industrial activated sludge basins, Nocardia-type and Microthrix parvicella filament foam events create stable floating scum that reduces oxygen transfer and complicates secondary clarifier weir control. M-640 is used as an emergency or scheduled foam-knockdown agent at a dosage of 1–10 ppm by volume on plant influent flow; the dosing point is the return activated sludge line or the mixed liquor channel upstream of the aeration basin, not the primary clarifier, because chemical oxygen demand contribution is minimized this way. The product is diluted to 1–5 vol% in plant water and injected with a peristaltic or diaphragm metering pump at a controlled rate; neat dosing into a single point produces a localized oil sheen and inconsistent knockdown. Effluent oil and grease is measured under ISO 9377-2, and biological treatment plants may require the defoamer to meet ready biodegradability screening under OECD 301B or an equivalent test. Terminal outputs are treated municipal or industrial effluent discharged under permit limits for BOD, TSS, and oil and grease, and dewatered waste activated sludge. The operational boundary is overdosing above 20 ppm, which has been associated with elevated effluent TPH and COD in plant monitoring data; for membrane bioreactor configurations, published data on this specific mineral oil defoamer is limited, and bench-scale mixed liquor compatibility testing is standard before full-scale duty.
Pressure-sensitive adhesive compounding places defoamer addition at the end of the mixing sequence, after tackifier dispersion inversion and cooling below 35 °C, because earlier addition forms oil-rich domains that interfere with tackifier resin particle coalescence. The process uses a low-shear anchor or gate-paddle mixer at 30–100 rpm; after pH adjustment and wetting-agent addition, the batch is placed under vacuum deaeration at -0.08 MPa to -0.09 MPa to remove entrained air. M-640 is added at 0.05–0.25 wt% on total wet adhesive mass, with higher doses reserved for high-solids packaging adhesives above 65% solids. For indirect food contact label and packaging adhesives, the compounded product must meet FDA 21 CFR 175.105 and EU regulation 1935/2004 as applied through member-state legislation, while REACH and California Proposition 65 recordkeeping apply for industrial shipments. Foam control is assessed by density measurement after vacuum deaeration and by air release under slow blade rotation; no separate foam-height test is routinely used for this application. Finished goods include paper label adhesives, envelope front seal adhesives, protective film re-wet and permanent laminating adhesives, and packaging tape adhesives. The upper dosing boundary is 0.30 wt%; beyond this point, migration of carrier oil may reduce 180° peel adhesion under ASTM D3330 and lower shear holding power under ASTM D3654 on low-energy film facestocks such as untreated polyethylene.
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M-640 General Purpose Mineral Oil Defoamer is supplied as a water-insoluble, surfactant-modified dispersion of hydrophobic fumed silica in refined mineral oil. The grade is positioned for foam control in aqueous polymer dispersions, water-based architectural coatings, pigment grinds, vinyl-acrylic and styrene-acrylic letdowns, water-based adhesives, and papermachine white-water systems of low to moderate severity. Unlike dissolved foam-control agents, M-640 operates by an interfacial mechanism: the mineral oil continuous phase spreads at the air–liquid interface, displaces the foam-stabilizing surfactant layer, and delivers the hydrophobic silica aggregates to the lamellae, where local thinning and a reduction in film elasticity cause bubble coalescence and gas release. The oil phase does not dissolve in the aqueous medium; it forms an unstable macroemulsion under agitation, and this shear-induced droplet-size distribution is the primary variable governing both knockdown speed and surface-defect risk.
The lot-release specification for M-640 should be verified against the supplier certificate of analysis before plant trials. The following ranges are class-representative values for general-purpose mineral oil/silica defoamers, not a batch-specific certificate.
| Parameter | Typical range or lot-release target | Method |
|---|---|---|
| Appearance | Off-white to pale amber opaque liquid | Visual inspection |
| Density at 20°C | 0.86–0.90 g/cm³ | ASTM D4052 / ISO 12185 |
| Viscosity at 25°C, Brookfield LV spindle 3, 20 rpm | 400–900 mPa·s | ASTM D2196 / ISO 3219 |
| Water content | ≤ 0.5% by mass | ASTM D6304 Karl Fischer |
| pH, 1% dispersion in deionized water | 6.0–8.5 | ISO 787-9 |
| Flash point, PMCC | > 150°C | ASTM D93 |
| Active content | ≥ 98.0% by mass | Supplier method |
| Ionic character | Nonionic emulsifier package | Supplier data |
| VOC contribution | System-dependent; evaluate formulation by ASTM D2369 | ASTM D2369 |
The viscosity range is not a single-point pipeline viscosity. The fumed silica network is thixotropic, and the low-shear Brookfield reading at 20 rpm may be 20–40% higher than the apparent viscosity at a shear rate of 100 s⁻¹. This shift is operationally significant: a progressive-cavity or diaphragm pump should be selected for metering, and centrifugal pumps should be avoided because local shear can strip the emulsifier and provoke silica agglomeration in the pump head.
The principal difference between M-640 and silicone-based defoamers is surface-tension reduction. Silicone systems based on polydimethylsiloxane reduce the dynamic surface tension of an aqueous formulation to the 20–24 mN/m range and typically deliver faster knockdown at lower dosage. M-640 as a mineral oil/silica system typically operates in the 28–32 mN/m range. The higher working surface tension reduces the probability of cratering and intercoat adhesion loss in pigmented architectural coatings, but it also means M-640 is less effective in clear or high-gloss systems where small amounts of residual surface oil are visible as haze or gloss loss. The product is therefore specified for general-purpose pigmented formulations rather than for optical-critical clear finishes.
Polyether/polyol defoamers based on ethylene oxide/propylene oxide block copolymers are water-dispersible and generally produce lower haze in clear films, but their defoaming action often depends on a cloud point or reduced solubility at the process temperature. In surfactant-saturated emulsion systems, the polyether may require a higher addition rate to match the same persistence. M-640 is less temperature-sensitive in ambient liquid systems between 20°C and 40°C because the active hydrophobic silica particles are preformed in oil; the performance does not rely on precipitation at a critical solution temperature. The trade-off is the presence of a mineral-oil residue that may affect adhesion or heat-seal performance in downstream converting.
| Attribute | M-640 mineral oil/silica | Silicone/polydimethylsiloxane | Polyether/polyol |
|---|---|---|---|
| Primary defoaming mechanism | Oil droplet spreading and hydrophobic particle film rupture | Low surface tension and spreading | Cloud-point precipitation and dewetting |
| Typical addition in pigmented latex coatings | 0.1–0.5 wt% | 0.05–0.3 wt% | 0.2–1.0 wt% |
| Knockdown profile | Moderate initial, persistent | Fast initial, persistent | Slow to moderate, dosage-dependent |
| Persistence under recirculation | Moderate to high | High | Moderate |
| Surface defect risk in clear or high-gloss systems | Low to moderate | Moderate to high | Low |
| Temperature dependence | Low in 20–40°C | Moderate | Higher, cloud-point dependent |
| Regulatory note | Mineral oil residue may affect food-contact and heat-seal tests | PDMS may affect silicone-sensitive substrates | Lower residue concern |
The comparative table is derived from industry screening work, not from direct substitution in a specific paint or latex formula. A resin-specific ladder study using the production letdown sequence and application method is required before replacing an incumbent defoamer.
In a 2000 L stainless steel dispersion vessel with a Cowles blade running at 12–15 m/s tip speed, the common failure mode is over-dispersion of the oil phase. If the full M-640 charge is added at the beginning of the pigment grind, the high-shear vortex reduces the oil droplet diameter below the critical size range needed for bubble-film bridging. The visible result is slower knockdown and the development of microfoam that appears as persistent pinholing in drawdowns and as haze in dried films. A more robust sequence is split addition: 50% of the calculated dose is added after the pigments have been wetted during dispersion, and the remaining 50% is added at the letdown stage under paddle agitation at 1–2 m/s tip speed. This preserves a sufficient population of larger oil droplets at the end of the batch and improves air release in the final coating.
The recommended addition range in water-based architectural coatings is 0.1–0.5 wt% on total formulation mass. In high-viscosity elastomeric formulations containing styrene-acrylic binder and high filler loading, the upper limit should be approached only after a resin-specific ladder study. Overdosing above 0.5 wt% in a clear low-pigment-volume binder can produce oil separation, surface haze, and reduced intercoat adhesion. Published data for this specific product configuration is limited; these limits are conservative screening boundaries, not fixed rheological thresholds.
Laboratory foam-tendency screening in styrene-acrylic latex is commonly performed with a blender foam test or a sparge-tube apparatus. A 0.2 wt% addition of this mineral oil/silica defoamer class may reduce foam height from above 500 mL to below 50 mL within 60 s under low-shear recirculation. The result cannot be transferred to high-solids alkyd or epoxy emulsions without revalidation because the surfactant phase and air-entry mechanism are different.
In semi-continuous styrene-acrylic latex production, the defoamer is not added during the nucleation stage. Hydrophobic oil droplets can seed secondary particles or promote microgel formation if introduced before the free monomer is fully converted. Addition is normally postponed to the post-polymerization letdown, when the free monomer level is below the manufacturer’s specified tolerance and the remaining anionic surfactant and mechanical agitation generate foam that can be controlled without disturbing the latex particle size distribution.
For continuous application in papermachine white-water loops or dissolved-air flotation skimmers, the product is usually injected neat through a positive-displacement pump into a point of turbulent flow. A flow velocity above 1.5 m/s at the injection point is desirable to distribute the oil droplets across the water volume without overshearing. If predilution is necessary for accurate metering, a 1:1 to 1:10 dilution with ambient service water may be prepared under low-speed paddle agitation; the prediluted emulsion should be used within 24 h because the emulsifier package is not designed for prolonged dilution stability. Adding the product to an activated sludge aeration basin requires caution: a mineral oil film at the air–water interface can reduce oxygen transfer efficiency by a system-dependent amount, so dosing should be linked to foam height and not fixed volumetric addition.
In papermaking, mill-specific food-contact documentation should be checked before use in grades covered by 21 CFR 176.200 or similar indirect food-contact regulations. A mill-specific extraction study is required because mineral oil defoamer residuals can influence paper porosity and heat-seal performance. REACH registration status, CLP classification, and any relevant harmonized exposure limits should be verified against the current safety data sheet for the lot supplied.
Store in sealed containers at 5–35°C. Below 5°C, the mineral oil continuous phase increases in viscosity and the fumed silica network becomes more resistant to flow; diaphragm or progressive cavity pumps should be used for metering, and centrifugal pumps should be excluded because local shear can destabilize the dispersion and cause silica agglomeration. Neoprene, nitrile, and PTFE seal materials are generally compatible; EPDM may swell on long exposure to mineral oil and should be avoided in pump and valve service.
If the material is exposed to a freeze–thaw cycle, it should not be returned directly to use. A reconditioning procedure of low-shear mixing at 50–100 rpm for 30–60 min in the original container or a dedicated stainless steel tank is the conservative starting point. High-shear redispersion after freezing can temporarily reduce viscosity but may create a stable microemulsion layer that reduces defoaming performance. Published data for freeze–thaw recovery of this specific M-640 configuration is limited; a batch should be qualified after any storage excursion outside the labelled range.
The pH of a 1% dispersion in deionized water is normally 6.0–8.5 by ISO 787-9. This range does not indicate that M-640 is a buffer; it only confirms that the emulsifier package is near neutral and that the product is not an acid- or alkali-catalyzed defoamer. The flash point by ASTM D93 PMCC is above 150°C, but the material remains combustible when heated above this point and should not be stored near strong oxidizers or open flames.
In water-based wood adhesives applied by roll coater, foam can accumulate in the recirculation tray and produce skipped adhesive lines. M-640 is added at 0.2–0.4 wt% after coalescing solvents are fully incorporated. If the adhesive film is subsequently heat-sealed, the mineral oil fraction can migrate to the surface and reduce heat-seal strength; a quantitative peel evaluation by ASTM F88 is required before production. The mineral oil defoamer is not a substitute for vacuum deaeration in filled, high-viscosity systems: it controls foam at the surface and in the bulk, but it does not remove dissolved gases from the liquid. The final addition level, injection point, and aging protocol should be established on the specific production line because published data for this specific configuration is limited.