Anhui Liwei Chemical Co,Limited
Section

Products

DOWSIL FS 1265 Fluorosilicone Oil Defoamer

    • Product Name: DOWSIL FS 1265 Fluorosilicone Oil Defoamer
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co,Limited
    • CONTACT NOW
    Specifications
    HS Code 242502
    Product DOWSIL FS 1265 Fluorosilicone Oil Defoamer
    Chemical Type 100% active fluorosilicone oil
    Appearance Clear to slightly hazy liquid
    Color Colorless to straw
    Viscosity At 25 C 300 cSt
    Specific Gravity At 25 C 1.25
    Refractive Index At 25 C 1.382
    Flash Point Open Cup 315 °C
    Pour Point -40 °C
    Surface Tension At 25 C 21.5 mN/m
    Solubility In Water Insoluble
    Active Content 100%

    As an accredited DOWSIL FS 1265 Fluorosilicone Oil Defoamer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing DOWSIL FS 1265 Fluorosilicone Oil Defoamer is supplied in 20 kg pails, ensuring convenient handling and controlled dispensing.
    Container Loading (20′ FCL) One 20′ FCL loaded with DOWSIL FS 1265 Fluorosilicone Oil Defoamer, secured, labeled, and stowed safely for export.
    Shipping DOWSIL FS 1265 Fluorosilicone Oil Defoamer ships in sealed, corrosion-resistant containers to prevent leakage. Transport dry, away from extreme heat, open flames, and incompatible oxidizers. Ensure adequate ventilation and secure upright loading. Follow all local, national, and international regulations for chemical transport, with appropriate hazard labeling and documentation.
    Storage Store DOWSIL FS 1265 Fluorosilicone Oil Defoamer in its original, tightly closed container in a cool, dry, well-ventilated area, away from direct sunlight, heat, sparks, and incompatible materials such as strong oxidizers. Maintain temperatures between 0°C and 40°C, protect from moisture, and ensure the container is sealed after each use to prevent contamination.
    Shelf Life Shelf life is 36 months from date of manufacture when stored in original, unopened container.
    Application of DOWSIL FS 1265 Fluorosilicone Oil Defoamer

    In high-solids solventborne alkyd coil coating topcoats, DOWSIL FS 1265 Fluorosilicone Oil Defoamer is introduced during the letdown phase to control air entrainment generated by reverse roll coater return flow. At production speeds of 60 to 120 m/min, the pick-up roll continuously reinjects paint from the pan into the nip; the resulting turbulent return entrains air into a binder phase already thickened by solvent evaporation. Dry film builds of 18 to 25 µm over hot-dip galvanized or 55% Al-Zn alloy-coated steel leave limited vertical distance for bubble rise before thermal crosslinking begins. High-solids coil alkyd vehicles commonly have acid numbers between 8 and 14 mg KOH/g and contain cobalt or zirconium driers that can stabilize fine air bubbles through surface-active oxidation by-products. Bubbles surviving the wet film expand as peak metal temperature approaches 232 °C, producing solvent pop, pinhole clusters, and loss of 60° gloss. The fluorosilicone defoamer is mixed at 0.05 to 0.15 wt% of total paint mass during letdown at cowles speeds of 500 to 800 rpm. Lower dosage frequently fails to clear fine pinholes; higher dosage lowers surface tension sufficiently to cause cratering over oily mill residues and intercoat adhesion loss beneath polyester backer or polyurethane topcoats. Quality release for coil-coated roofing and wall cladding is assessed under ASTM D523-14(2018) at 20° and 60°, ASTM D3359-23 Method B, and ASTM D2369-20 for VOC content. Because the defoamer is a non-volatile fluorosilicone fluid, it does not add directly to VOC mass measured by ASTM D2369-20, but retained surface-active material must be confirmed through recoatability panels before full-scale coil campaigns.

    What Causes Persistent Microfoam in Two-Part Epoxy Zinc-Rich Primers?

    In two-part zinc-rich epoxy primers, persistent microfoam arises from the combined effects of high pigment volume concentration, rapid viscosity build after mixing, and surface-active fractions of polyamidoamine hardeners. The base component typically contains bisphenol A diglycidyl ether or novolac epoxy with an epoxide equivalent weight between 180 and 220 g/eq, zinc dust at more than 60 wt% of the dry film, and an organoclay thixotrope. After mixing with a polyamidoamine or cycloaliphatic amine hardener, viscosity rises from approximately 1,000 to 2,500 cP at 25 °C, trapping air introduced during plural-component airless spray application at fluid pressures of 3,000 to 5,000 psi. DOWSIL FS 1265 is introduced as a split addition because the high-shear pigment grind and low-shear letdown phase require different defoamer residence times. Starting addition is 0.1 to 0.3 wt% of the total mixed system, with 70% of the defoamer charge incorporated during pigment dispersion and 30% during final letdown. This sequence controls pinholes in dry films of 75 to 100 µm over Sa 2½ blasted steel while reducing the risk of surface enrichment that impairs overcoating. Foam-related defects are evaluated under ASTM D714-17 blistering, ASTM D3359-23 cross-cut adhesion, and ISO 4624:2016 pull-off adhesion. The cured primer is intended as a zinc-rich passive-sacrificial base for structural steel in bridges, offshore platforms, and tank farms; selection of the primer system is evaluated according to ISO 12944-5:2019 protective coating system requirements. Direct addition of the defoamer to the hardener alone should be avoided because phase separation may occur before the components are combined under field mixing conditions.

    Solventborne moisture-cure polyurethane wood flooring systems present a separate foam mechanism that cannot be eliminated by vacuum deaeration alone: the isocyanate-water reaction generates carbon dioxide continuously during film cure. Aromatic isocyanate prepolymers with free NCO content between 6% and 8% are cut in butyl acetate, xylene, and propylene glycol monomethyl ether acetate, applied by roller at 100 to 150 g/m², and cured at ambient relative humidity. Viscosity is normally held between 25 and 40 s Ford #4 at 25 °C. The defoamer is used at 0.03 to 0.1 wt% of total coating mass to suppress carbon dioxide macrofoam without arresting the controlled microfoam release needed to prevent gas entrapment below the surface skin. Overdosing causes the defoamer to collapse bubbles too close to gelation, leaving pinholes that rupture after the film surface has already closed. Quality control is anchored to ISO 2813:2014 for 60° gloss retention, ISO 1520:2006 cupping resistance, and ASTM D4060-19 Taber abrasion. The terminal product is a one-component moisture-cure polyurethane topcoat for residential wood flooring, gymnasiums, and select prefinished wood goods where fast return to service after application is required.

    When Airless Spray Atomization Nucleates Solvent Vapor in Acrylic Refinish Basecoats

    When a medium-solids acrylic refinish basecoat is sprayed through an airless tip of 0.28 to 0.33 mm at fluid pressures between 1,200 and 1,800 psi, the sudden pressure drop across the orifice creates supersaturation of the solvent blend. Dissolved air and solvent vapor nucleate as fine bubbles in the atomized film and can be retained on the substrate if the basecoat flashes too rapidly. DOWSIL FS 1265 is used at 0.05 to 0.2 wt% of total basecoat mass to break foam lamellae before film closure, with the addition made after the metallic pigment slurry has been dispersed and under low-speed mixing at 100 to 200 rpm. In basecoats containing aluminum flake pigments, overdosing lowers surface tension unevenly across the film and disturbs flake orientation, causing mottling or halo formation after clearcoat application. Conversely, underdosing produces pinholes that become visible after clearcoat cure. The formulated basecoat is evaluated for 20° gloss with ASTM D523-14(2018), cross-cut adhesion to a two-component primer or E-coat with ASTM D3359-23, and viscosity by Zahn #2 cup using ASTM D4212-16. VOC content is determined by ASTM D2369-20 for regional automotive refinish compliance, and the defoamer contributes no volatile solvent fraction under that test method. The terminal configuration is a basecoat/clearcoat system for collision repair and specialty vehicle refinishing, where cycle time, film appearance, and color stability are the dominant acceptance criteria.

    Solventborne flexographic and gravure inks generate a characteristic foam profile at the doctor blade return and pump suction side because the inks are formulated at low viscosity and circulated under turbulent flow. Nitrocellulose, polyamide, or polyvinyl butyral binders dissolved in ethyl acetate, ethanol, n-propanol, and propyl acetate produce viscosity normally between 18 and 25 s Zahn #2 at press temperature. At line speeds of 150 to 300 m/min, foam carry-over into the anilox metering volume or gravure cell causes print voids, pinhole defects, and apparent color loss on treated BOPP or polyethylene film substrates with wetting tension between 38 and 42 dyn/cm. DOWSIL FS 1265 is used at 0.05 to 0.2 wt% of finished ink mass. In alcohol-rich flexographic ink blends, the fluorosilicone defoamer may begin to separate if added directly as a neat fluid; pre-dilution in ethyl acetate or n-propyl acetate at a 1:1 or 1:2 ratio before introduction to the mixing vat reduces phase-separation risk. Overdosing can lower ink surface tension to the point where the doctor blade film-forming character changes and metered film thickness becomes erratic. For printed flexible packaging intended for food contact, the converter must establish functional barrier performance or specific migration compliance under EU 10/2011 or FDA 21 CFR 175.300; no automatic food-contact status is granted for this industrial fluorosilicone defoamer. The terminal product is a printed laminate or overwrap film used in snack, confectionery, and household product packaging.

    High-Pigment-Volume Epoxy-Polyamide Maintenance Coating Recoatability After Defoamer Overdose

    High-pigment-volume epoxy-polyamide maintenance topcoats applied by airless spray over aged shop primer or feathered edges are sensitive to retained defoamer because the coating is frequently overcoated with an aliphatic polyurethane UV-resistant finish. DOWSIL FS 1265 is used at 0.05 to 0.2 wt% of total mixed coating to control air entrapment from the high-viscosity polyamide component and from surface turbulence during spray application. At levels above approximately 0.3 wt%, the fluorosilicone fluid can migrate to the coating-air interface and remain there after cure; this is aggravated when the polyamide hardener contributes amine blush or exudation. The recoat window for such maintenance systems is commonly 24 h to 7 days at 25 °C; beyond this window, surface preparation may require mechanical abrasion. The evaluation sequence for overcoating acceptance includes pull-off adhesion under ASTM D4541-22, cross-cut adhesion under ASTM D3359-23, and gloss retention under ASTM D523-14(2018). Surface cleanliness of the steel substrate prior to the maintenance coat is verified according to ISO 8501-1, with near-white blast cleaning to Sa 2½ typically specified. Terminal use is a corrosion-control topcoat on process vessels, structural steel, tank exteriors, and bridge components, where repeated overcoating over long service intervals is a fundamental design requirement.

    Compliance checklist matrix for recoatability evaluation of epoxy-polyamide maintenance coating systems
    Property EvaluatedStandard DesignationMeasurement Condition
    Cross-cut adhesionASTM D3359-23 Method Bparallel cuts at 2 mm spacing
    Pull-off adhesionASTM D4541-22self-aligning dolly; 1 MPa/s loading rate
    Dry-film thicknessISO 2808:2019eddy current method on ferrous substrate
    Specular glossASTM D523-14(2018)60° geometry
    Blister resistanceASTM D714-17post-condensation exposure
    Free Quote

    Competitive DOWSIL FS 1265 Fluorosilicone Oil Defoamer prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615380400285 or mail to sales2@liwei-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@liwei-chem.com

    Inquiry

    Get Free Quote of Anhui Liwei Chemical Co,Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    DOWSIL FS 1265 Fluorosilicone Oil Defoamer is a 100% active fluorosilicone oil based on poly(trifluoropropylmethylsiloxane). The product identifier FS 1265 designates the 1000 mm²/s viscosity grade within the DOWSIL fluorosilicone defoamer range. Kinematic viscosity at 25 °C is controlled to 1000 mm²/s when measured according to ASTM D445-23. Specific gravity at 25 °C is 1.24 under ASTM D4052-22, and the surface tension is approximately 24 mN/m under ASTM D1331-20. Refractive index at 25 °C is 1.380 under ASTM D1218-21. The product is supplied as a clear, essentially colourless liquid for formulation into non-aqueous foam-control systems, particularly solventborne coatings, printing inks, adhesives and industrial fluids where foam is stabilised by aromatic or oxygenated solvent loading.

    Because the fluid is 100% active and not self-emulsifying, it must be predispersed in a compatible solvent or introduced under mechanical shear. The product does not contain added emulsifiers, thickeners, or carrier solvents; as a result, its behaviour in a finished formulation is governed by droplet size and solvent partitioning rather than by surfactant migration. This differentiates FS 1265 from many ready-to-use defoamer preparations that are supplied as emulsions or dispersions. The product is not a finished defoamer compound in the sense of a pre-stabilised additive package; it is an oil-based active substance that requires defined dispersion work on production-scale mixing equipment.

    What Limits Foam Stabilization in High-Aromatic Solvent Coatings?

    Foam stabilisation in high-aromatic solvent coatings occurs when solvent evaporation and resin polarity increase surface viscosity. Entrained air bubbles acquire a surface-active resin layer that impedes lamella drainage. The fluorosilicone oil has a lower surface tension than the foaming liquid and limited solubility in aromatic and oxygenated solvents; it enters the lamella, spreads, displaces resin stabilisers, and causes rupture. The decisive parameters are droplet diameter, spreading coefficient and the solubility parameter mismatch between the defoamer and the continuous phase. In xylene-based and butyl acetate-based coating systems, the fluoropropyl substituent reduces the tendency of the defoamer to dissolve into the bulk resin solution, thereby preserving discrete low-surface-energy droplets at the air–liquid interface.

    In a high-shear dispersion stage with a Cowles blade operating at tip speeds between 10 m/s and 15 m/s, the additive is reduced to droplets with a median diameter below 20 µm when monitored by laser diffraction per ISO 13320:2020. Droplets larger than 40 µm can settle or form visible surface oil; droplets smaller than 5 µm may become over-compatibilised and reduce film clarity without adequate foam knockdown. The processing window therefore requires defined shear time and not merely total addition rate. If dispersion is stopped too early, foam control is inconsistent; if dispersion continues after full droplet development, the additional shear contributes no further knockdown benefit and may increase batch temperature, altering solvent loss in open mixing vessels.

    Typical physical property panel for DOWSIL FS 1265 Fluorosilicone Oil Defoamer
    PropertyTypical valueTest standard
    AppearanceClear, colourless to pale straw liquidVisual inspection
    Kinematic viscosity at 25 °C1000 mm²/sASTM D445-23
    Specific gravity at 25 °C1.24ASTM D4052-22
    Refractive index at 25 °C1.380ASTM D1218-21
    Surface tension24 mN/mASTM D1331-20
    Active content100%Supplier specification

    Critical Addition Thresholds and Film Defect Boundaries

    In air-drying alkyd gloss enamels, the typical addition range is 0.1 wt% to 0.3 wt% by total batch weight. Below 0.05 wt%, foam knockdown may be insufficient in high-solids formulations with viscosities above 1500 mPa·s at 25 °C under ISO 2884-1. Above 0.4 wt%, cratering and loss of image distinction are commonly observed when gloss is measured under ASTM D523-14 and distinctness of image under ASTM D5767-18. These thresholds are system-dependent and must be established on production equipment because laboratory drawdowns do not reproduce the same shear history, solvent flash or film thickness. Published data for specific resin systems is limited; the cited ranges represent practical formulation boundaries rather than absolute specification limits.

    In 2K polyurethane clearcoats, addition after hardener mixing but before final dilution reduces gas bubble entrapment. However, the product may reduce recoatability if not fully incorporated before spraying. The low surface tension of the fluorosilicone oil persists through solvent evaporation; if the oil is present as oversized droplets or insufficiently distributed, surface defects can appear after forced drying at 60 °C to 80 °C. Compatibility must therefore be confirmed by visual inspection and optical evaluation on the production line. Batch-to-batch viscosity variation of the defoamer is controlled within ±50 mm²/s at 25 °C in the supplier specification; wider deviation can shift droplet size distribution under identical dispersion conditions.

    In solventborne flexographic and gravure inks containing high levels of aromatic hydrocarbons or ketones, conventional dimethylsiloxane defoamers may dissolve sufficiently into the bulk phase to become inactive. FS 1265 retains a solubility parameter mismatch due to the trifluoropropyl substituent, maintaining discrete droplets at addition levels up to 0.2 wt%. This causes stronger lamella rupture in high-solvent ink varnishes but also increases the likelihood of surface defects if ink film thickness exceeds 12 µm. Flow time after storage at 40 °C for 28 days may be assessed according to ISO 2431:2019; formulations containing FS 1265 typically retain more stable flow behaviour than equivalent dimethylsiloxane-containing controls, although head-to-head data for this product is limited and must be confirmed on the target ink line.

    When Fluorosilicone Replaces Dimethylsiloxane in Non-Aqueous Ink Systems

    Polyether-modified siloxanes are self-emulsifying and generally produce fewer film compatibility defects but are less effective against macrofoam in high-aromatic solvents. FS 1265 requires mechanical dispersion but provides stronger persistent knockdown at equivalent active content. The choice between the two must include haze, gloss and intercoat adhesion testing because the fluorosilicone oil is less spontaneously distributed than siloxane copolymers. In clear coatings, a difference of only 0.1 wt% can shift a formulation from acceptable foam control to visible surface disruption; dose optimisation should therefore be conducted at the upper half of the intended film thickness range.

    The fluorosilicone surface tension of approximately 24 mN/m is higher than that of many dimethylpolysiloxane oils, but the stronger solvent rejection in polar non-aqueous media is the more relevant performance attribute. Dimethylsiloxane oils can swell in aromatic solvents and lose interfacial activity, while the fluorosilicone remains phase-separated. This distinction becomes important in high-speed printing where foam is generated by solvent evacuation, ink return flow and rapid cylinder rotation. In such systems, FS 1265 is introduced as a diluted stream into the recirculating ink rather than as a one-time batch addition; this prevents local high concentration from producing fish eyes on printed substrates.

    Thermal Degradation Pathways in Fluoropropylmethylsiloxane Under Refluxing Aromatic Solvents

    At solvent reflux temperatures in xylene or butyl acetate, the fluorosilicone oil retains foam-control performance for longer than silicone polyether defoamers because fluorinated side groups reduce solvent-induced swelling. However, exposure to alkaline catalysts or strong acids accelerates siloxane chain scission. In epoxy floor coatings catalysed with amine hardeners, the defoamer should be incorporated into the resin component before hardener addition to minimise contact with free amine under exothermic cure. The upper processing temperature for this product is generally 200 °C for short dwell times; published data for prolonged exposure above 150 °C in amine-containing systems is limited.

    Storage in sealed containers at temperatures between 5 °C and 40 °C is recommended; moisture ingress can produce haze in the bulk liquid but does not normally alter foam-control performance. The product is not formulated for direct addition to waterborne systems. If an aqueous end-use is required, conversion into a stable emulsion with a suitable surfactant is necessary; direct addition to a latex or water-reducible coating can cause fisheyes, emulsion destabilisation, or incomplete dispersion. The product must be validated under the specific resin, solvent, pigment and shear conditions of the target manufacturing line before production use.