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SILFOAM SE 23 30% Active High-Concentration Silicone Antifoam Emulsion

    • Product Name: SILFOAM SE 23 30% Active High-Concentration Silicone Antifoam Emulsion
    • 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 926819
    Product Name SILFOAM SE 23
    Active Ingredient Silicone antifoam compound
    Active Content 30%
    Form High-concentration aqueous emulsion
    Appearance White to slightly grayish milky liquid
    Ionic Character Nonionic
    Viscosity At 25c Approximately 500 - 1000 mPa·s
    Ph At 25c Neutral to slightly alkaline, approximately pH 7 - 8
    Density At 25c Approximately 1.0 g/cm³
    Solubility Or Dispersibility Readily dispersible in water
    Dilutability Can be diluted with water to lower active concentrations
    Temperature Stability Stable and effective in foam control up to at least 100°C
    Shelf Life Minimum 12 months from date of production when stored properly
    Storage Temperature Store between 5°C and 40°C in sealed original containers

    As an accredited SILFOAM SE 23 30% Active High-Concentration Silicone Antifoam Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing SILFOAM SE 23 is packaged in 200 kg (net) unlined steel drums with sealed lids, ensuring safe transport and storage.
    Container Loading (20′ FCL) 20′ FCL container loading of SILFOAM SE 23, 30% active silicone antifoam emulsion, safely packed and secured for transport.
    Shipping SILFOAM SE 23 ships as a non-hazardous, water-based silicone emulsion. Pack in sealed drums or IBCs, protected from freezing and extreme heat. Avoid prolonged direct sunlight. Ensure secure upright loading, with adequate ventilation and spill containment. Store between 5–35°C; shake or agitate before use if separation occurs.
    Storage Store SILFOAM SE 23 in its original, tightly closed container in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible materials like strong oxidizers. Avoid freezing; ideal storage temperature is between 5°C and 35°C. If unopened and properly stored, shelf life is typically 12 months. Ensure container remains sealed to prevent contamination.
    Shelf Life Shelf life is typically 12 months from manufacture if stored in original unopened containers at 5–30°C; avoid freezing and contamination.
    Application of SILFOAM SE 23 30% Active High-Concentration Silicone Antifoam Emulsion

    SILFOAM SE 23 is supplied as a high-active silicone antifoam emulsion containing 30% polydimethylsiloxane by weight. The concentrate is normally diluted with demineralized water at a ratio of 1:5 to 1:10 before dosing into aqueous process streams, because direct addition of the high-active form can create localized oil films in low-turbulence zones. Dilution should be performed with ambient water between 20°C and 25°C using low-shear agitation only; high-speed dispersers can break the emulsion and reduce knockdown efficiency. The material functions by spreading at the air–liquid interface, disrupting the surfactant-stabilised foam lamella and accelerating bubble coalescence. In concentrated electrolytes, strong alkalis, or solvent-rich formulations, the emulsion may cream or separate during extended storage; homogeneity is restored by slow stirring rather than violent mixing. Indirect food contact uses require verification under the applicable positive list, such as FDA 21 CFR 176.210 for paper and paperboard processing aids. The following application tracks represent the relevant downstream processing environments for this high-active emulsion.

    Application sectorTypical concentrate additionPrimary verification parameterFinal article
    Continuous jet dyeing0.1–0.5 g/LISO 105-C06, oil spot inspectionDyed polyester/cotton knit
    Architectural paint0.05–0.2 wt%ISO 1524, ISO 2813Vinyl acrylic wall paint
    Alkaline CIP washing5–15 µL/LASTM D3601, ATP bioluminescenceCleaned food-contact surface
    Brown stock washing0.2–0.8 kg/t dry fiberFDA 21 CFR 176.210, washer vacuumBleached pulp sheet
    Activated sludge aeration2–20 ppmISO 8192, trans-membrane pressureTreated effluent
    Agrochemical formulation0.5–2.0 g/LCIPAC MT 47.2, ISO 13320Pesticide suspension concentrate

    High-Turbulence Foam in Continuous Jet Dyeing and Exhaust Dyeing Machinery

    In polyester and cotton knit processing on jet dyeing machines, foam generation is driven by air ingestion at the Venturi constriction and by residual surfactants from scouring and leveling auxiliaries. When SILFOAM SE 23 is pre-diluted with cold demineralized water at 1:5 and added to the dyebath after the substrate is wetted but before addition of dyes and electrolytes, the concentrate typically achieves control at 0.1–0.5 g/L depending on total surfactant load and jet pump pressure. In high-temperature disperse dyeing above 130°C, the emulsion droplets are exposed to thermal and shear stress inside the circulation pump for up to 45–60 min; overdosing beyond approximately 0.8 g/L can produce localized silicone deposition on polyester because droplets coalesce and adhere to hydrophobic fiber surfaces. This failure mode is more pronounced when the bath contains carrier solvents, oligomer dispersants, or high electrolyte concentrations above 30 g/L sodium sulfate. The practical control method is split dosing: one-third of the required amount is added at the start of the cycle, one-third after salt addition, and one-third after the first unload check, which limits the maximum emulsion concentration in any single phase of the process. Final dyed fabric should be evaluated for oil spots by inspection under UV illumination after drying at 120°C for 3 min, and wash fastness can be checked according to ISO 105-C06 to ensure that silicone residues do not alter the colour-fastness rating. Pump cavitation and float chamber malfunction are the primary process indicators for antifoam failure, not visual foam height alone.

    What Limits Letdown Defoamer Performance When the Emulsion Is Added After Pigment Grind?

    Architectural paint manufacturing on a high-speed disperser introduces air at the vortex around the disc, and the resulting microfoam is stabilised by wetting agents, dispersing agents, and associative thickeners present in the mill base. If SILFOAM SE 23 is added only during letdown after the pigment grind is completed, the high active silicone droplets may remain too large to wet out low-surface-energy resin particles effectively, and macroscopic craters or fisheyes can appear in the dried film. The preferred processing sequence is to add 0.05–0.2 wt% of the concentrated emulsion to the pigment slurry during the grind stage under a cowl or vacuum shroud, where the tip speed of the disperser disc typically reaches 10–18 m/s; the high shear breaks the defoamer into submicron droplets that are more uniformly distributed. A second portion can be added during letdown, but only after dilution at 1:10 with water and under low-shear stirring below 5 m/s to avoid destabilizing the emulsion and creating silicone agglomerates. The mill base grind should be checked with a Hegman gauge according to ISO 1524, and the final film should be drawn down and inspected against a control for surface defects. Gloss retention and haze are measured by ISO 2813 and ISO 13803, while over dosage above 0.5 wt% can cause intercoat adhesion loss, particularly in waterborne alkyd or polyurethane topcoats. Laboratory compatibility panels should be performed at 23°C and 50% relative humidity for 24 h before production approval. The final architectural product is typically a vinyl acrylic or acrylic latex wall paint with a VOC content below 30 g/L as determined by ISO 11890-2, and the silicone defoamer contributes no measurable VOC to the formulation.

    Alkaline bottle-washing and clean-in-place sequences for food processing equipment generate persistent foam from saponified fat soils, protein hydrolysates, and formulated nonionic surfactants such as alcohol ethoxylates and alkylpolyglucosides. In this application SILFOAM SE 23 is dosed into the wash tank after the detergent concentrate has been diluted to its use concentration, typically between 5 µL/L and 15 µL/L relative to the wash liquor, because direct addition to the concentrated detergent may destabilize the emulsion in the presence of high electrolyte and caustic levels above 10% NaOH. The product suppresses foam by spreading a polydimethylsiloxane monolayer at the air–water interface, but the high active content means that the emulsion must be distributed rapidly across the tank surface by return-pipe turbulence or a spray ball; local overfeeding can create an oily surface film that interferes with conductivity probes and optical foam sensors. In tunnel washers, antifoam consumption is linked to saponification load: heavily soiled crates produce higher foam and require the upper half of the dosing range, while lightly soiled bottles require the lower half. The use level should not exceed 25 µL/L in rinse water because silicone carryover to the final rinse can impair the wettability of stainless steel surfaces and may fail subsequent water-sheet inspection according to internal plant specifications. The wash liquor can be monitored for foam persistence by the bottle-shake method ASTM D3601, and final rinsed surfaces are checked for residual soil by an ATP bioluminescence meter rather than by visual inspection alone. For detergent formulations intended for indirect food contact cleaning, the formulator should verify that the antifoam is cleared under the applicable regional regulation or that a food-grade silicone alternative is used in the final product.

    When Brown Stock Washer Foam Overflows the Screen Room, Silicone Carryover Becomes the Critical Constraint

    In a kraft pulp mill the brown stock washing line receives black liquor at 70–90°C from the digester blow tank, where tall oil soaps, lignin degradation products, and residual white liquor generate stable foam that reduces washing efficiency and can overflow the foam tower into the screen room. SILFOAM SE 23 is injected into the blow tank or the first-stage washer seal tank at 0.2–0.8 kg per ton of dry fiber, depending on softwood/hardwood ratio, black liquor solids, and the amount of soap skimming upstream. The product is primarily used as a knock-down defoamer at the washer, not as a persistent defoamer for the black liquor storage tanks, because extended residence time in hot alkaline liquor can degrade the emulsion and reduce its efficiency. The primary application risk is silicone carryover from the pulp mat into the bleach plant or the paper machine, where hydrophobic deposits on forming fabrics and press felts cause sheet defects and reduced dewatering. Mills commonly set a maximum residual defoamer concentration in the screened stock of 50 mg/kg dry fiber and measure deposit tendency by Soxhlet extraction of pulp with a nonpolar solvent, followed by gravimetric or FTIR analysis. In food-contact paper and paperboard grades, the use of silicone defoamers as processing aids falls under FDA 21 CFR 176.210, and the final article must meet extractive limitations under 21 CFR 176.170 for the intended food type. Process control is based on foam height in the washer seal tank, washer vacuum drop, and black liquor carryover measured as chemical oxygen demand of the pulp mat wash water; a sudden increase in COD carryover often indicates antifoam overdosing because excess silicone can blind the pulp mat and reduce displacement efficiency. The final bleached pulp sheet is tested for brightness, dirt count, and extractives according to TAPPI standard methods, but no single method fully captures silicone deposition on mill clothing.

    Diffused Aeration Basins Require Pulse Dosing to Avoid Silicone Surface Film and Membrane Fouling

    Excessive foaming in an activated sludge aeration basin is commonly associated with filamentous organisms such as Microthrix parvicella, high mixed liquor suspended solids, or incoming surfactant loads from industrial discharge. SILFOAM SE 23 can be applied to the basin surface through a spray bar or to the mixed liquor at the aeration inlet at a dosage of 2–20 ppm based on basin volume, but the minimum effective dose must be determined by jar testing because higher doses can form a coherent surface film that reduces oxygen transfer from fine-bubble diffusers. The product is not a biocide and does not remove the filamentous bacteria; it only controls the associated foam generated by stabilised air bubbles and hydrophobic cell surfaces. In membrane bioreactor systems, continuous dosing above approximately 5 ppm can accelerate fouling of polyvinylidene fluoride or ceramic membranes because the silicone droplets adsorb onto the membrane surface and increase trans-membrane pressure. Operators typically pulse-dose the antifoam at intervals of 30–60 min rather than continuously, and monitor dissolved oxygen concentration, oxygen uptake rate, and trans-membrane pressure trends before and after each dosing event. The effect of the antifoam on the activated sludge microbial community is assessed by inhibition testing according to ISO 8192, which measures respiration inhibition; the concentration causing 50% inhibition should be well above the planned basin dose. Discharge permits generally do not set limits for silicone, but a visible surface sheen in the clarifier or final effluent is an operational boundary that indicates overdosing and must trigger dose reduction. The final treated effluent is monitored for suspended solids, biochemical oxygen demand, and turbidity under standard methods such as ISO 7027 for turbidity; antifoam carryover is inferred from surface film formation rather than a specific silicone analytical method.

    Aqueous suspension concentrate, microemulsion, and soluble concentrate pesticide formulations are filled on high-speed piston or rotary filling lines where air entrainment and surfactant-stabilised foam can reduce net fill volume and cause nozzle splash. The 30% active SILFOAM SE 23 emulsion is typically incorporated into the formulation after the active ingredient slurry has been milled and before final viscosity adjustment, at a concentration of 0.5–2.0 g/L of formulated product. It must be added under low-shear mixing because high-shear dispersion after addition can destabilize the emulsion and produce visible silicone oil droplets in the packaged product. The most commonly evaluated foam parameter for agrochemical formulations is persistent foam height and collapse time, measured by the CIPAC method MT 47.2; formulations intended for tank mixing should produce no more than 10 mL of persistent foam after the specified shaking and settling period. Compatibility of the defoamer with the suspending system is verified by accelerated stability storage at 54°C for 14 days, followed by measurement of suspension stability, wet-sieve residue, and re-dispersibility according to CIPAC methods. In diluted tank mixtures, the active silicone droplets can flocculate with lignosulfonate or naphthalene sulfonate dispersants; the tank mix should be visually inspected for oiling-out and phase separation at 1% dilution in both standard hard water and CIPAC water A. Droplet size after dilution is measured by laser diffraction according to ISO 13320, and a shift in the volume median diameter above 5 µm relative to the undiluted formulation may indicate emulsifier incompatibility. The final packaged agricultural product must be stable in the original container for a minimum shelf life, with no oil layer greater than 1 mm after 30 days at ambient storage. In all cases the active ingredient label controls, and the defoamer must not be included above the level specified in the confidential statement of formula for the registered product.

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    Certification & Compliance
    More Introduction

    SILFOAM SE 23 is a 30 wt% active high-concentration silicone antifoam emulsion supplied as a water-dilutable oil-in-water dispersion. The product designation identifies a concentrated silicone system in which the hydrophobic antifoam phase is pre-emulsified in water. In contrast to low-active emulsions in the 10–20 wt% range, the 30 wt% active content shifts the mass balance across the supply chain: for a fixed active silicone requirement, the required emulsion mass is reduced by 50% relative to a 15 wt% active emulsion and by 67% relative to a 10 wt% active emulsion.

    Routine lot-release parameters for this class of water-thin silicone emulsions are determined by calibrated glass-electrode pH per ISO 10523:2012, rotational viscosity with a Brookfield spindle at 25°C per ISO 2555, and density by pycnometer per ISO 2811-1. The manufacturer’s certificate of analysis is the controlling document for exact viscosity, density, and pH. The active content of 30 wt% is not numerically interchangeable with gravimetric total solids under ISO 3251; volatile siloxane components and non-silicone stabilizer materials can cause the two values to diverge. Particle size distribution, where required, may be measured by laser diffraction per ISO 13320:2020. The product does not require high-pressure homogenization before use because the silicone oil phase is already dispersed into the aqueous continuous phase.

    What Distinguishes a 30 wt% Active High-Concentration Emulsion from Dilute Silicone Antifoam Grades?

    At the formulation level, the primary difference is water load. A 10 wt% active emulsion introduces 9 kg of water for every 1 kg of active silicone; a 20 wt% product introduces 4 kg water; a 30 wt% formulation introduces 2.33 kg water. This difference changes rail and tote logistics, tank inventory, and the amount of dilution water reaching the process. The concentration should not be misread as automatic performance superiority; foam-control efficiency depends on droplet size after dilution, surfactant compatibility, and the shear history of the feed stream.

    Comparative dosing arithmetic for emulsion antifoam active concentration classes
    Parameter10 wt% active emulsion20 wt% active emulsion30 wt% active emulsion (SILFOAM SE 23)
    Mass required to deliver 1 kg active silicone10 kg5 kg3.33 kg
    Water introduced per 1 kg active9 kg4 kg2.33 kg
    Continuous dose at 100 ppm active in process fluid1000 ppm emulsion500 ppm emulsion333 ppm emulsion
    Relative inventory volume at equal active mass, assuming similar density reference1.5× reference reference

    This arithmetic quantifies delivery concentration only. Equal active mass does not guarantee equal foam suppression because silicone emulsions vary in internal phase viscosity, particle size distribution, and the presence of hydrophobic silica or other dewetting solids. The selection of a concentrated grade is therefore justified primarily by logistics, storage space, and water-volume constraints rather than by an assumption of higher intrinsic performance.

    Besides water content, the pre-dispersed form differentiates SILFOAM SE 23 from undiluted silicone antifoam compounds and organic defoamers. Undiluted silicone fluids typically require high-shear or solvent pre-mixing to create the contact-angle geometry needed for film rupture. The emulsion is delivered with the oil phase already dispersed; however, the water phase makes it freeze-sensitive, which is not a limitation for solvent-based defoamers. Compared with ethylene oxide/propylene oxide block copolymer defoamers, silicone emulsions generally operate at lower mass dosages, but their surface activity can persist on finished substrates; wetting and cratering tests should therefore be included in the evaluation.

    In continuous aqueous process streams, the emulsion is metered by positive-displacement dosing pump after dilution to a 1–10 wt% working dispersion in demineralized or soft water. Dilution should be performed under moderate low-shear agitation. Rotor-stator mixers are not required and may destabilize the diluted emulsion if local shear exceeds approximately 3000 s⁻¹. The working dispersion should be consumed within 24 h unless the user validates longer stability by particle size analysis or zeta potential measurement. Published data specific to SILFOAM SE 23 post-dilution shelf life are limited; end-user feed systems require site-specific use-before timelines. Pumps and lines are selected for compatibility with silicone fluids; fluoropolymer tubing and stainless steel are commonly used, while EPDM elastomer swelling may be evaluated by immersion testing per ISO 1817.

    Rheological and Interfacial Requirements in High-Shear Processing

    High-shear aqueous operations include jet dyeing machines with pump flow rates above 1000 L/min and nozzle pressures of 1–3 bar, paper coating circulation loops using rotor-stator mixers, and spray cleaning systems operating at 80–90°C and 10–15 bar. In these environments, the antifoam emulsion must pass through narrow orifices, centrifugal pump stages, and back-pressure valves without splitting into an oil phase. Concentrated silicone emulsions near 30 wt% active content can be more sensitive to shear-induced coalescence than dilute grades because the dispersed oil droplets are more crowded. For this reason, dilution before the high-shear zone is preferred.

    The antifoam mechanism depends on the entering and spreading coefficients of the silicone oil at the air-water interface. The entering coefficient is defined as E = γ_A/W + γ_W/O − γ_O/A, and the spreading coefficient is S = γ_A/W − γ_O/A − γ_W/O, where γ_A/W is aqueous surface tension, γ_O/A silicone surface tension, and γ_W/O water-oil interfacial tension. Positive values describe thermodynamic favorability for the oil to enter and spread on the foam lamella; surfactants in the foaming medium can reduce γ_A/W enough to make both coefficients negative, which is one reason antifoam performance is system-dependent. Once the oil spreads, hydrophobic silica particles embedded in the oil phase can dewet at the gas-liquid interface and rupture the foam film. The process is kinetic as well as thermodynamic; the oil must reach the lamella surface within the short residence time of a foam film in a high-shear machine.

    Because of that mechanism, static bottle-shake screening using ASTM D3601-20 provides only a first pass. It does not reproduce the continuous foam regeneration, wetting, shear, and air entrainment present in jet dyeing machines or coating circulation loops. A meaningful evaluation for SILFOAM SE 23 in these systems should include a shear-history protocol in a pilot-scale jet loop or a rotor-stator circulation rig with controlled back-pressure and temperature. Foam collapse time, pump suction stability, and surface deposit formation are recorded at three addition levels: 0.01 wt%, 0.05 wt%, and 0.10 wt% active in the process fluid. If the process fluid contains high levels of nonionic surfactants, the antifoam demand may shift upward, but the risk of hydrophobic deposits on finished surfaces also increases.

    Dosing levels are typically expressed as mass fraction of emulsion in the foaming medium. In batch dyeing, a preliminary dilution to 5 wt% active is often used and fed by metering pump into the suction side of the main circulation pump. The suction-side addition point uses the main pump to mix the emulsion without creating a separate high-shear dispersion step. In paper coating and surface-sizing formulations, the product is added downstream of pigment slurry preparation and binder letdown to limit contact with high-solids mineral dispersions. The addition point should be located downstream of screens and homogenizers where possible. Overdosing can create hydrophobic deposits on fabric, paper, or coating surfaces; the observed threshold is formulation-dependent, but process evaluation commonly begins below 100 ppm active. Published threshold data specific to SILFOAM SE 23 in individual coating chemistries are limited, so production-scale trials remain the definitive evidence.

    When the Emulsion Is Injected into Hot Alkaline Cleaning Baths

    Alkaline industrial cleaning and metalworking baths may operate at pH 9–13 and temperatures from 50°C to 85°C. Under these conditions, electrolytes can compress the electrical double layer on emulsion droplets and induce coagulation, creaming, or oiling out. A concentrated 30 wt% active emulsion should not be injected as a neat stream into the hot caustic tank because rapid local destabilization can form an oil layer on the liquid surface. The recommended approach is to dilute to a 1–5 wt% working dispersion at ambient temperature and then meter into the suction side of the circulation line. If the bath contains dissolved solids above approximately 10 g/L sodium hydroxide or equivalent ionic strength, a bench-scale compatibility study should be performed before production use. Turbidity, visual creaming, and particle size change over 24 h are appropriate stability indicators. Published data for this exact product in strong alkali at high temperature are limited, and end-user compatibility testing is required to establish the operating boundary.

    Storage of the unopened product should maintain the emulsion at 5–40°C, protect against direct sunlight, and exclude frost. Ice crystal formation can rupture the oil-water interface and produce irreversible cream or oil separation. If freezing has occurred, the product should not be rehomogenized on site unless validated by particle size analysis under ISO 13320:2020 and by lot-specific emulsion stability testing. Opened containers are sealed immediately after use to minimize water loss, which would increase apparent active concentration. Short-term viscosity increase caused by water evaporation is not a valid indicator of active silicone degradation. Bulk containers should be gently recirculated or drum-tumbled before use; high-shear mixing is unnecessary and may introduce air bubbles.

    Standards and Methods Do Not Replace Site-Specific Validation

    Routine evaluation matrix for aqueous silicone antifoam emulsions
    Property or requirementMethod or standardRole
    Foam suppression in aqueous mediaASTM D3601-20Bottle-shake screening only; not a substitute for high-shear pilot testing
    pH of aqueous emulsionISO 10523:2012Batch-release and storage stability check
    ViscosityISO 2555Routine QC and feed-pump sizing
    DensityISO 2811-1Dosing-meter calibration and tank inventory verification
    Particle size distributionISO 13320:2020Shear-damage and post-dilution stability evaluation
    Gravimetric solidsISO 3251Not equivalent to 30 wt% active silicone content
    Elastomer compatibilityISO 1817Pump tubing and gasket material selection
    Regulatory dossierREACH (EC) No 1907/2006; CLP (EC) No 1272/2008Confirm current manufacturer SDS and country-specific requirements

    The matrix identifies methods suitable for this emulsion class; it does not establish that SILFOAM SE 23 carries a specific regulatory approval in any end-use category. For food-contact, potable water, or pharmaceutical applications, the manufacturer’s current regulatory certification should be obtained and checked against the relevant national or regional positive list before use.