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DEFOM W-086 Mineral Oil Defoamer for Waterborne Coatings & Adhesives

    • Product Name: DEFOM W-086 Mineral Oil Defoamer for Waterborne Coatings & Adhesives
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co,Limited
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    Specifications
    HS Code 202050
    Product Name DEFOM W-086 Mineral Oil Defoamer for Waterborne Coatings & Adhesives
    Product Type Mineral oil-based defoamer
    Appearance Milky white to light yellow viscous liquid
    Chemical Composition Mineral oil with hydrophobic silica and emulsifying agents
    Active Content 100%
    Viscosity At 25c 300-800 mPa·s
    Specific Gravity At 25c 0.88-0.95
    Flash Point Above 150°C
    Water Dispersibility Easily dispersible in water
    Ionic Character Non-ionic
    Recommended Dosage 0.1%-0.5% based on total formulation weight
    Defoaming Performance Rapid foam knockdown and long-term foam suppression
    Compatibility Compatible with acrylic, styrene-acrylic, vinyl acetate, and other waterborne latex systems
    Shelf Life 12 months when stored in original sealed container at 5-35°C

    As an accredited DEFOM W-086 Mineral Oil Defoamer for Waterborne Coatings & Adhesives factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Available in 5-gallon pails and 55-gallon drums, sealed to prevent contamination and ensure product stability.
    Container Loading (20′ FCL) Container Loading (20′ FCL): One 20-foot full container load of DEFOM W-086 mineral oil defoamer for waterborne coatings and adhesives.
    Shipping DEFOM W-086 ships in sealed drums or pails to prevent moisture ingress and contamination. Keep containers upright, secured, and protected from freezing or excessive heat during transit. Classified as a non-hazardous mineral oil blend, standard chemical handling and spill precautions apply. Avoid direct sunlight and store in a dry, well-ventilated area.
    Storage Store DEFOM W-086 in its original, tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Protect from freezing and extreme temperatures. Keep container upright to prevent leaks. Under recommended conditions, shelf life is typically 12 months from manufacture. Always reseal tightly after use.
    Shelf Life Store in original container, away from extreme heat or cold. Shelf life is 12 months from date of manufacture.
    Application of DEFOM W-086 Mineral Oil Defoamer for Waterborne Coatings & Adhesives

    In interior semi-gloss architectural topcoats formulated with styrene-acrylic binders at 50 g/L VOC or lower, entrained air during Cowles high-shear dispersion and low-shear roller application generates microfoam that lowers distinctness of image and scrub resistance. DEFOM W-086 is typically introduced as a split addition: 0.05–0.10 wt% in the grind phase before TiO₂ dispersion and 0.05–0.20 wt% in the letdown phase after binder addition, giving a total of 0.10–0.30 wt% on total formulation. The grind-phase addition suppresses air incorporation during pigment dispersion at 15–20 m/s tip speed in a Cowles disperser, while the letdown addition controls coalescence of residual microfoam during room-temperature film formation. Compliance for interior wall paints is evaluated under ASTM D562 for Stormer viscosity, ASTM D2805 for hiding power, ASTM D523 for 60° gloss, and US EPA Method 24 for VOC content. Terminal product types include interior semi-gloss wall and trim paints in 3.78 L containers and 18.9 L pails, applied by 9.5 mm nap rollers and airless spray units. Over-addition above 0.30 wt% produces surface defects in the form of craters and fisheyes on non-porous primed drywall and reduces 60° gloss by 3–6 units in ASTM D523 measurements due to mineral oil enrichment at the air-coating interface. Plant experience indicates that prolonged incorporation in a high-speed disperser above 20 m/s tip speed shears the hydrophobic silica particles and reduces deaeration efficiency by 20–40% within 30 min, necessitating re-inoculation at the letdown stage.

    Exterior Elastomeric Wall Coating Defoaming Under High PVC and Thick-Film Application

    High-build acrylic elastomeric exterior coatings with PVC between 35% and 55% and dry film thickness up to 500 µm require a defoamer that can release air from high-viscosity, high-solids systems without compromising wet adhesion to concrete and masonry. DEFOM W-086 is added at 0.20–0.50 wt% of total formulation, typically split between the calcium carbonate/kaolin pigment grind and the final thickener adjustment. In production, a high-speed disperser with a 45° tooth blade operating at 18–25 m/s tip speed entrains far more air than standard architectural paints due to higher extender load; a silicone-free mineral oil defoamer is preferred to avoid intercoat adhesion loss. Standards for elastomeric wall coatings include ASTM C1305 for crack bridging, ASTM D6083 for liquid-applied elastomeric coatings, and ASTM D2370 for elongation. Terminal finished products include 5-gallon pails of elastomeric wall coating applied by 19–32 mm roller or airless spray at 160–220 bar to bridge hairline cracks. Over-addition beyond 0.50 wt% lowers wet adhesion on fiber-cement siding and creates pinholes during hot-weather application above 40°C surface temperature, as the mineral oil phase migrates to the film surface before crosslinking of the acrylic latex. Published data for this specific configuration is limited; plant trials with a 1000 kg batch size showed that a single-point addition at the thickener letdown step was insufficient to suppress microfoam, producing a 12% loss in tensile elongation after ASTM D2370 conditioning.

    Why Does Air Release Fail in Spray-Applied Waterborne Wood Lacquers?

    In a 30:1 air-assisted airless system delivering 200–250 mL/min at 80–120 bar fluid pressure, the coating circulates through a 6 m x 3/8 in hose, generating fine bubble size distributions below 100 µm that are stabilized by associative polyurethane thickeners. DEFOM W-086 is added at 0.10–0.25 wt% based on total formulation, preferentially after final viscosity adjustment at 20–25°C, and incorporated for 15–20 min at 5–8 m/s tip speed in a low-shear sweep mixer. Addition in the sand mill is avoided because the high-shear environment above 10 m/s ruptures the hydrophobic silica droplets and reduces foam knockdown in subsequent spray booth trials. Compliance in wood coating systems relies on ASTM D3359 for adhesion, ASTM D4366 for film hardness, ASTM D2244 for color consistency, and DIN EN 71-3 for migration of certain elements where furniture coatings are used on children's articles. Terminal product types include waterborne acrylic-alkyd hybrid furniture lacquers and clear topcoats applied by HVLP at 1.8–2.2 bar atomizing air to kitchen cabinet doors, chairs, and engineered wood panels. Incompatibility with acetoacetate-functional crosslinkers has been recorded when the defoamer concentration exceeds 0.30 wt%: the mineral oil phase interferes with film formation at 50–60 µm wet film thickness, producing persistent craters and a reduction in König pendulum hardness by 8–12% after 7-day cure.

    Waterborne acrylic pressure-sensitive adhesive formulations destined for transfer coating onto 25 µm PET release liners and subsequent lamination to 80 g/m² kraft paper face stock are highly sensitive to entrained air because bubbles arrested in the 10–15 µm adhesive film leave pinholes that reduce loop tack and darken the dried film under reflected light. A mineral oil defoamer is metered into the letdown vessel at 0.10–0.40 wt% of total adhesive solids prior to viscosity adjustment with an alkali-soluble thickener, and the batch is homogenised at 80–120 rpm in a 2000 L planetary mixer for 30 min. Addition during the initial monomer emulsion or polymerisation step is prohibited because the hydrophobic silica particles can nucleate gel micro-seeds and raise coagulum levels above 50 ppm in the finished latex. Compliance for tape and label applications is anchored to PSTC-101, ASTM D6195 loop tack, ASTM D3654 shear adhesion at 23°C and 50% RH, and FDA 21 CFR 175.105 where the adhesive is used in indirect food packaging. Terminal product types include 2-mil transfer tapes, removable repositionable labels, and freezer-grade box sealing tapes converted on 1300 mm-wide rotary die-cutting lines. Operational boundary: when the adhesive is diluted below 500 mPa·s with water for curtain coating, the defoamer's mineral oil droplets can coalesce and float, causing inhomogeneous foam knockdown; inline filtration through 150 µm mesh is required to remove agglomerates larger than 200 µm that otherwise create coating streaks.

    When Food-Contact Laminating Adhesives Demand Low Foam at 150 m/min Line Speeds

    If flexible packaging laminators running retortable structures such as PET/Al foil/CPP at line speeds of 120–200 m/min are to maintain foam-free adhesive films below 3 µm dry coat weight, foam collapse after drying must be prevented because it opens channels that compromise barrier performance and cause delamination during 121°C retort cycles. The mineral oil defoamer is added at 0.20–0.50 wt% based on dry adhesive solids in the final dilution stage, after catalyst addition and before pH adjustment to 6.5–7.5 with ammonia. In high-speed gravure coating, the adhesive bath in a closed doctor blade chamber recirculates at 20–30 L/min, generating foam at the return line; a metered 0.02–0.05 wt% continuous top-up maintains foam height below 5 mm in the coating pan. Compliance in EU and US food-contact structures references EU 10/2011 with specific migration limits for mineral hydrocarbons MOSH/MOAH, FDA 21 CFR 175.105 and 177.1390 where applicable to the adhesive layer, and REACH Article 33 declarations for mineral oil components. Terminal finished products include retort pouches, stand-up barrier pouches, and lidding films for ready-meal trays, converted on 1300 mm-wide slitter-laminators. Incompatibility with high-acid filling above pH 4.5 has been observed when mineral oil migrates from the adhesive into the food simulant; migration testing per EU 10/2011 Annex V with 3% acetic acid for 10 days at 40°C should be conducted at the minimum dry coat weight. Published data for this specific defoamer under retort conditions is limited; plant-scale trials at a 3 µm dry film weight showed that excess defoamer above 0.50 wt% caused interlayer delamination at the PET/Al interface after 30 min at 121°C, measured by ASTM F904.

    Beverage Can Interior Spray Lining and Foam Control During Dead-End Filtration

    At 35,000–60,000 cans/h, interior epoxy-acrylate and acrylic waterborne beverage can linings are spray-applied through electrostatic high-rotation bell atomizers; foam in the supply line from 200 L pressure tanks causes pulsation and uneven film distribution across the can bottom and dome. A silicone-free mineral oil defoamer is preferred at 0.10–0.25 wt% of total liquid coating to avoid electrode contamination in electrostatic application. The coating is processed through 5 µm dead-end bag filters at 1.5–2.5 bar differential pressure; entrained air can be removed by vacuum degassing at 50–80 mbar for 10 min after defoamer addition, but over-agitation above 500 rpm reintroduces bubbles. Compliance for beverage can interior linings relies on FDA 21 CFR 175.300 for resinous and polymeric coatings, EU Regulation 10/2011, and REACH SVHC screening, with mineral oil purity requirements under 21 CFR 178.3620 for the defoamer carrier. Terminal products include aluminium beverage can two-piece interior linings and easy-open end coatings, applied at 120–180 mg/355 mL can film weight and cured in 200–205°C ovens for 45–60 s. Operational boundary: mineral oil defoamers cannot be used in ultraviolet-curable can coatings because the oil phase inhibits free-radical photopolymerisation at the surface and causes oxygen inhibition; the user must switch to a polyether-modified siloxane type for UV formulations. A 5 mg/m³ aerosol exposure limit under OSHA PEL for mineral oil mist requires local exhaust ventilation at the spray booth.

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    Certification & Compliance
    More Introduction

    DEFOM W-086 is a mineral oil-based foam-control agent formulated for waterborne coatings and adhesive systems. The model designation W-086 denotes a pourable liquid in which a refined mineral oil carrier is compounded with dispersed hydrophobic particles and nonionic emulsifiers. The product is not a silicone defoamer; its function depends on particle-laden oil droplets that enter the air–liquid foam lamella, bridge the film between adjacent air cells, and trigger rupture. Intended binder systems include acrylate, styrene-acrylate, vinyl acetate-ethylene, and polyvinyl acetate dispersions where entrained air, surface macrofoam, and microfoam reduce wet-film quality, film density, and bond strength. Published batch-specific physical property data for this exact model is limited; the values presented below are representative acceptance limits for this mineral-oil defoamer class and must be checked against the supplier certificate of analysis.

    What incoming QC limits control DEFOM W-086 acceptance in a waterborne coatings plant?

    Raw material release for a mineral-oil defoamer of this grade typically evaluates appearance, density, Brookfield viscosity, pH of an aqueous dispersion, nonvolatile content, and phase stability after temperature cycling. Incoming inspection commonly uses ISO 2811-1 for liquid density, ISO 2555 for apparent viscosity, and ISO 976 for pH of polymer dispersions. The acceptance envelope in Table 1 is a representative internal QC matrix; the controlling document remains the DEFOM W-086 certificate of analysis.

    Representative incoming QC matrix for mineral-oil defoamer grade W-086
    ParameterTest methodAcceptance rangeNotes
    AppearanceVisualPale yellow to amber opaque liquidNo free oil separation after 24 h
    Density at 25 °CISO 2811-10.85–0.93 g/cm³Pycnometer method
    Brookfield viscosity at 25 °CISO 2555300–1,200 mPa·sSpindle 3, 20 rpm
    pH of 2% aqueous dispersionISO 9765.0–7.5Neutral to slightly acidic
    Nonvolatile contentISO 3251>98%105 °C, 2 h
    Freeze-thaw stabilityVisual after 3 cyclesNo irreversible separationCycle −5 °C to 25 °C

    Functional dosage in waterborne architectural paints is commonly 0.1–0.3 wt% of total formulation. Flat interior paints with high pigment volume concentration and high surfactant load may require 0.3–0.5 wt%. In semi-gloss systems below 25% PVC, addition above 0.15 wt% can reduce 60° specular gloss measured by ASTM D523 by more than 5 points relative to the control. Therefore the operational dosage window is narrower in low-PVC systems, where the defoamer droplet population competes with the smooth air-liquid interface of the dried film.

    In production on a high-speed disperser equipped with a Cowles blade at 18–25 m/s tip speed, DEFOM W-086 is preferably introduced as a split charge: 50% in the grind and 50% in the letdown. Addition of the full amount before pigment dispersion may subject the mineral-oil droplets to prolonged high shear, stripping nonionic emulsifier from the droplet surface and reducing foam knockdown after thickener addition. Letdown incorporation at <1,000 rpm for 10–15 min is generally sufficient to distribute the defoamer without creating coarse oil droplets.

    Macrofoam knockdown, microfoam persistence, and surface defect thresholds remain distinct performance fields

    Entrained air in a waterborne coating exists in two forms that respond to different mechanisms. Macrofoam is visible at the wet-film surface and is removed rapidly by defoamer droplets that migrate to the air–liquid interface. Microfoam consists of small bubbles that do not rise before film collapse; these bubbles can produce pinholes when the coating is force-dried or baked. A defoamer optimized only for knockdown may not eliminate microfoam. DEFOM W-086 contains dispersed hydrophobic particles sized to penetrate the foam lamella and provide both rapid surface knockdown and partial microfoam reduction in pigmented semi-gloss systems. For force-dried coatings applied at 60 °C for 30 min, residual microfoam should be evaluated under 20× magnification after film application by ASTM D823.

    Foam rupture is controlled by the dewetting of hydrophobic particles at the gas–liquid interface. Effective foam-control particles exhibit a three-phase contact angle above 90°. Particles with contact angles below 60° tend to remain wetted by the continuous phase and may stabilize foam rather than rupture it. When a mineral-oil droplet reaches the lamella, the oil spreads at the surface and creates a local surface-tension gradient that drains the film. The rupture rate is influenced by oil drop diameter, which in waterborne paint is typically maintained between 10 μm and 50 μm by the emulsifier package. Droplets above 100 μm may coalesce into visible surface oil and produce craters, intercoat adhesion loss, or gloss reduction. Cross-cut adhesion after recoating can be evaluated by ASTM D3359; acceptable performance in interior semi-gloss systems is generally 4B–5B.

    Defoamer addition can alter the low-shear viscosity of associative thickener systems. In a HEUR-thickened acrylic paint, addition of 0.3 wt% mineral-oil defoamer may reduce low-shear viscosity by 10–25% as measured by ISO 2555 at 10 rpm, because the oil droplets compete with associative thickener hydrophobic groups. Thickener adjustment should be made only after the defoamer dosage has been fixed; otherwise final rheology may drift across batches.

    When mineral oil defoamer substitutes silicone in semi-gloss and clear waterborne systems

    Mineral-oil defoamers differ from silicone and polyether products in surface activity, compatibility, and defect profile. Silicone defoamers based on polydimethylsiloxane have lower surface tension, often 20–22 mN/m, and are more efficient against microfoam in low-PVC systems. Their high surface activity can cause cratering and recoatability defects if over-added. Mineral-oil grades such as W-086 have surface tension values closer to 28–32 mN/m, which reduces the severity of cratering while retaining macrofoam knockdown. This makes mineral-oil products more commonly used in flat and satin architectural paints, waterborne construction dispersions, and adhesives where silicone-induced surface defects are unacceptable. In clear wood coatings, mineral-oil defoamers may produce haze; compatibility screening at 0.1% addition on sealed Leneta charts using ASTM D4062 is required before full-line use.

    Comparative performance profile of foam-control chemistries in waterborne acrylic semi-gloss paint
    ChemistryMacrofoam knockdownMicrofoam eliminationCratering tendencyHaze in clear filmRecoatability risk
    Mineral oil with hydrophobic particlesHighModerateLow to moderateModerateLow at <0.2 wt%
    Polydimethylsiloxane siliconeHighHighHighLowVariable
    Polyether or polyether-modified siloxaneModerateLow to moderateLowLowLow

    Compared with other DEFOM defoamer grades based on silicone or polyether chemistry, W-086 is selected for pigmented waterborne systems where macrofoam during letdown and filling operations is the dominant defect. It is less efficient against sub-surface microfoam than a silicone concentrate, but its lower spreading pressure reduces the probability of fish eyes and recoating failures. The mineral-oil platform also shows lower persistence in highly surfactant-loaded systems, so dosage may require upward adjustment when the formulation contains anionic emulsifiers above 0.5 wt% on binder solids.

    High-shear dispersion protocols in PVAc and acrylic emulsion adhesive manufacture

    Waterborne adhesives impose different constraints because bubble removal must occur during mixing and roller application without leaving an oil film at the bond line. For polyvinyl acetate wood adhesives with solids of 45–55%, DEFOM W-086 is added at 0.2–0.4 wt% based on wet adhesive. The defoamer reduces air entrainment during high-speed mixing, but over-addition can migrate to the surface and reduce tack. Shear strength of bonded wood specimens can be checked by ASTM D905. In acrylic pressure-sensitive adhesive formulations, addition above 0.5 wt% may reduce loop tack and peel; application-specific limits should be determined by ASTM D3330 for peel adhesion and ASTM D3654 for shear holding power.

    In a 500 L planetary mixer operating at 20–30 rpm blade speed, the defoamer is added after the polymer dispersion but before fillers and thickeners to allow uniform distribution without excessive shear. Mixing for 10 minutes after defoamer addition generally produces a homogeneous dispersion. For continuous adhesive lines using rotor-stator mixers at 3,000 rpm, the defoamer should be injected downstream of the high-shear zone to preserve droplet integrity. If the rotor-stator unit is placed before defoamer injection, entrained air generated by the high-shear zone can be removed more efficiently, but droplet breakage from the rotor-stator may reduce persistence.

    Operational boundaries for DEFOM W-086 include storage between 5 °C and 40 °C in closed HDPE containers. At temperatures below 5 °C, viscosity increases and the product may gel; slow-speed agitation at 20–25 °C restores flow. Storage in unlined mild steel is not recommended because mineral oil may extract iron and darken the product. The product is not intended for solvent-borne coatings, UV-curable systems, or two-component polyurethane systems containing highly polar solvents, because the mineral oil may remain as an incompatible liquid phase and reduce intercoat adhesion. Over-emulsification with nonionic surfactants having HLB above 16 can solubilize hydrophobic particles into micelles and deactivate defoaming. The product should not be combined with silicone defoamers in the same addition port; competing surface mechanisms may produce syneresis rather than foam control.