| HS Code | 747840 |
| Appearance | Milky white homogeneous liquid |
| Active Silicone Content | 30% |
| Viscosity 25 C | 500–1500 mPa·s |
| Ph 1 Aqueous Solution | 6.0–8.0 |
| Density 25 C | 0.98–1.02 g/cm³ |
| Solubility In Water | Self-emulsifying, forms stable dispersion |
| Ionic Type | Non-ionic |
| Recommended Dosage | 0.1–0.5% of total formulation |
| Foam抑制 Rate | ≥90% |
| Storage Stability | 12 months in sealed container at 5–35°C |
| Freeze Thaw Stability | Stable for 5 cycles without separation |
| Flash Point | >100°C |
As an accredited KS-538 Self-Emulsifying Silicone Defoamer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | KS-538 Self-Emulsifying Silicone Defoamer is packaged in 200 kg plastic drums, with stable quality, easy pouring, and safe transport. |
| Container Loading (20′ FCL) | 20' FCL container loading of KS-538 defoamer: drums/pails palletized, secured, labeled, with proper ventilation and spill containment. |
| Shipping | KS-538 ships in sealed, corrosion-resistant drums or IBCs, ensuring safe transit. Store upright in a cool, dry, ventilated area away from heat, ignition sources, and strong oxidizers. Handle with standard chemical protection. Prevent spills; if leakage occurs, contain and dispose per local regulations. Avoid freezing; keep shelf life under 12 months. |
| Storage | Store KS-538 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep containers tightly sealed to prevent contamination and evaporation. Recommended storage temperature is 5–35°C; avoid freezing. Maintain original packaging and use within 12 months. Stir gently before use if separation occurs. |
| Shelf Life | KS-538 Self-Emulsifying Silicone Defoamer has a typical shelf life of 12 months when stored in original, sealed containers under recommended conditions. |
In 55–65% PVC interior wall paints and water-based flexographic inks, KS-538 is introduced at 0.1–0.5 wt% of total formulation mass, split between the pigment grind and the letdown phase. The defoamer functions by forming a low-surface-energy polydimethylsiloxane film at the air–water interface; hydrophobic silica particles penetrate the foam lamella and accelerate bubble coalescence. In a 2,000–3,000 rpm cowles disperser, air entrainment reduces apparent viscosity and can cause pump cavitation in in-line tinting equipment; the addition of 0.2 wt% KS-538 in the letdown restores a bubble-free rheology profile as measured by a cone-and-plate viscometer at 10,000 s⁻¹. Because the product is self-emulsifying, it can be post-added without a high-shear premix, but stored material at 40°C for 28 days should be conditioned with a low-shear paddle sweep of 50–100 rpm to re-homogenize the emulsion. Overdosing beyond 0.5 wt% of total formulation mass is the principal processing risk: silicone migration to the surface of a dried acrylic film reduces 60° specular gloss as determined by ASTM D523-20, and cratering becomes visible under 45° incident light inspection. Foam control efficiency is evaluated by ASTM E2407-04(2023) with a foam collapse time below 15 s at 25°C. For low-VOC architectural compliance, batch release includes ASTM D6886-18 VOC determination; the defoamer itself contributes no measurable volatile organic compound under this method. End products include interior wall paints, water-based flexographic inks, and concentrated tint bases where foam control must survive multiple freeze–thaw cycles according to ASTM D2243-20.
Semisynthetic metalworking fluid concentrates diluted to 5–8 vol% in 150–400 ppm hard water receive KS-538 at 0.05–0.15 wt% of the sump charge. Foam generation in high-pressure coolant delivery at 70–100 bar through a 0.5–1.0 mm nozzle causes pump cavitation, reduced lubricity transfer, and increased tool wear; the defoamer lowers foam height from above 20 mm to below 5 mm in the ASTM D3601-88(2019) aqueous media bottle test. The product’s self-emulsifying character is critical in central sump systems with make-up water hardness fluctuation: it disperses without forming an oily ring at pH 8.5–9.5, whereas non-self-emulsifying silicone oils may separate and blind filter media with pore sizes of 10–20 µm. The processing conflict is overdosing above 0.3 wt% of the diluted fluid, which can destabilize the ester-based emulsifier package and reduce emulsion droplet size uniformity as measured by laser diffraction; this produces a visible surface sheen and increases tramp oil entrapment. Defoamer addition is made directly to the return line of the central sump under turbulent flow, not at the high-pressure pump suction, to avoid localized concentration spikes. End products include ferrous alloy cutting and grinding operations where the coolant is filtered through hydrocyclones and paper-bed filters with 15–25 µm nominal retention. No defoamer-related residue on machined parts has been observed when the addition level remains below 0.2 wt%, but at higher levels, a silicone film may interfere with subsequent alkaline cleaning and phosphate conversion coating.
Polyester woven fabric processed in a 1:8 liquor ratio jet dyeing machine at 120–135°C under 1.5–2.0 bar pressure receives KS-538 at 0.02–0.1 g/L of dyebath. The jet dyeing machine’s venturi and circulation pump generate high-shear foam, which causes fabric lift and tangling in rope form; the self-emulsifying silicone defoamer collapses broth foam without depositing hydrophobic silicone spots on the fabric surface. The product is added after the dyebath reaches 60°C and before the addition of disperse dyes to avoid interaction with the dye dispersant package. Compatibility is maintained in pH 4.5–5.5 acetate buffer; outside this window, silicone emulsion inversion may occur and produce a visible slick on the bath surface. A critical process control is the rinse phase: residual defoamer at levels above 0.05 g/L in the final rinse can reduce fabric wettability and subsequent water-based finishing pad pickup, so an overflow rinse of 10–15 min at 80°C is specified. End products include dyed polyester and polyester–elastane woven goods, where final fabric is evaluated for silicone spot defects under D65 illuminant and for absorbency according to AATCC TM79-2018. The defoamer does not interfere with reduction clearing using sodium hydrosulfite at 80°C for 20 min, provided the dyebath is drained and the fabric is rinsed before the reduction clear step. For mill discharge compliance, chemical oxygen demand contribution of the defoamer is measured by ISO 6060:1989.
When a 480 g/L chlorothalonil suspension concentrate diluted 1:200 in CIPAC D water is agitated in a 200 L spray tank with a recirculation pump, foam can reach 10–15% of tank headspace and cause inconsistent spray volume delivery. KS-538 is incorporated into the formulation at 0.05–0.3 wt% during bead milling after the active ingredient slurry has been wetted with the nonionic block copolymer dispersant. The self-emulsifying silicone defoamer provides rapid deaeration in the spray tank; the target is a foam collapse time below 10 s in the CIPAC MT 47.2 persistent foam test. Because the product is not a mineral-oil-based additive, it is screened in greenhouse phytotoxicity trials on maize and soybean; inert-ingredient tolerance is verified under EPA 40 CFR 180.910. The formulation process requires pH adjustment to 6.5–7.5 before defoamer addition; acidic conditions below pH 5.0 can destabilize the silicone emulsion and produce visible oil separation in the millbase. Overdosing above 0.3 wt% may reduce suspension viscosity and accelerate particle settling in 500 mL graduated cylinders under 54°C storage. End products include water-based suspension concentrates, suspoemulsions, and soluble liquid formulations where foam control is specified in the registration dossier.
Municipal sludge digesters operating at 35–38°C and 3–5% total solids exhibit surface foam when lipid loading and free fatty acid concentrations exceed the digester’s biomass assimilation rate; the foam layer reduces active working volume and can block gas collection lines. KS-538 is metered into the recirculation loop at 1–5 ppm by digester mass using a peristaltic pump with a 0.5–2.0 L/h dosing range; the self-emulsifying product disperses in the pH 6.8–7.6 sludge without forming a floating oil film. The defoamer collapses filament-induced foam by reducing surface elasticity, which allows biogas to disengage from the liquid phase; gas production is monitored with a positive-displacement flow meter and is not used as a direct control signal because foam events lag hydraulic loading by 8–12 h. A critical boundary is that dosing above 5 ppm can adsorb onto methanogenic flocs and reduce substrate transfer, lowering specific methanogenic activity as measured by ISO 11734:1995; therefore the addition is started at 1 ppm and increased only when foam height exceeds 30 cm in the digester sight glass. Published data for this specific combination of KS-538 and digestate substrates is limited; treatability studies at 1–5 ppm are required before full-scale use. End products include treated sludge digestate and biogas; digestate destined for land application must still meet metal concentration limits in EPA 40 CFR Part 503. The defoamer does not alter ammonia nitrogen or volatile fatty acid profiles under routine gas chromatography monitoring.
At the wet end of a neutral papermaking machine running 1,200 m/min, foam in the headbox and wire pit reduces first-pass retention and entrains air, causing pinholes in the sheet and reduced drainage. KS-538 is applied at 0.1–0.5 kg/ton dry fiber through a chemical dosing skid with a progressive cavity pump; the addition point is the tray water return line, not the fan pump suction, so that the defoamer is distributed across the entire white-water loop. The self-emulsifying silicone product is effective at pH 6.5–8.5 and at white-water temperatures of 40–55°C, conditions typical of closed water recirculation. The process conflict is overdosing above 0.5 kg/ton, which can increase sizing agent consumption and reduce sheet coefficient of friction; papermakers correct this by trimming the dose in 0.05 kg/ton increments while monitoring headbox air content with a gas-displacement sensor. For food-contact paper and paperboard, the defoamer must comply with FDA 21 CFR 176.210 as a defoaming agent used in the manufacture of paper and paperboard; a certificate of composition confirming dimethylpolysiloxane and silica content is maintained in the mill’s food-contact documentation. End products include kraft linerboard, food-contact folding carton stock, and coated printing paper where surface defects are graded under the mill’s internal optical scanning system with sensitivity below 0.5 mm².
| Regulatory citation | Scope | Required documentation |
|---|---|---|
| FDA 21 CFR 176.210 | Defoaming agents used in the manufacture of paper and paperboard | Certificate of composition listing polydimethylsiloxane and silica |
| EU 1935/2004 | Food contact materials general safety | Declaration of compliance with overall migration limits |
Alkaline CIP cleaners containing 5–10 wt% sodium hydroxide and 2–5 wt% sodium metasilicate generate foam during high-pressure spray cleaning in dairy and beverage processing; the foam reduces mechanical impact on soiled surfaces and can damage seals in rotary spray heads. KS-538 is formulated into the cleaner concentrate at 0.05–0.2 wt% and remains stable for 90 days at 25°C in the alkaline matrix. The self-emulsifying silicone defoamer suppresses foam in the recirculation tank and allows the cleaner to be used at 0.5–1.5 vol% dilution without excessive foam carryover into the rinse step. The product must not leave a hydrophobic residue on stainless steel surfaces; after simulated CIP cycles with 0.5 vol% cleaner at 70°C for 20 min, panels are inspected by the water-break-free test according to ASTM F22-21. The critical boundary is silicone deposition above 0.3 wt% in the concentrate; this can create a water-repellent film that interferes with sanitizer contact and ATP bioluminescence hygiene monitoring. The cleaner is regulated under EU Detergent Regulation (EC) No 648/2004 and must list silicone defoamer in the ingredient data file; the product does not contribute to phosphorous loading. End products include single-use CIP detergents, acid-alkaline two-step cleaners, and conveyor lubricants where foam control is specified for 2–5 bar spray pressures.
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KS-538 Self-Emulsifying Silicone Defoamer is a nonionic silicone-based foam-control agent supplied as an off-white to white viscous liquid. The product disperses spontaneously in aqueous media at 25 °C when exposed to mild agitation. Unlike conventional silicone oils that require high-shear emulsification before use, KS-538 is formulated with an internal emulsifier system that yields an oil-in-water emulsion on contact with water. Typical application environments include latex manufacturing, pigment slurry preparation, cooling water circuits, and wastewater operations where macrofoam and entrained air reduce pump efficiency and filtration throughput. The formulation is intended for continuous or semi-continuous dosing; batch addition without sufficient agitation may result in localized oiling at the addition point. The model designation KS-538 distinguishes this self-emulsifying grade from solvent-extended and mineral-oil-modified defoamers.
The active defoaming species in KS-538 is a polydimethylsiloxane fluid. The silicone phase lowers surface tension and spreads at the air-liquid interface, displacing foam-stabilizing surfactants. In high-surfactant media, the product functions by bridging and dewetting of foam lamellae, as described in industrial antifoam literature. The self-emulsifying property is imparted by a nonionic emulsifier package; the resulting droplet size distribution determines both knock-down speed and persistence. The nonionic emulsifier package has an HLB value in the range 8–11, which is typical for self-emulsifying oil-in-water systems. Because the product is nonionic, its performance is less affected by dissolved calcium and magnesium salts than anionic emulsified defoamers.
The silicone fluid exhibits a surface tension of approximately 20–22 mN/m at 25 °C, which drives spreading at the air–water interface of foam lamellae. For a droplet to act as an effective antifoam, the entering coefficient and spreading coefficient must both be positive; these coefficients depend on the dynamic surface tension of the foam-stabilizing surfactant solution and the viscosity of the silicone oil. However, at pH above 11, alkaline hydrolysis of the siloxane polymer and the emulsifier can reduce both knock-down speed and persistence. The product should not be pre-diluted with water for storage; dilution should be carried out immediately before use because the self-emulsified dispersion has limited storage stability. A 1 % dispersion in deionized water typically exhibits a milky appearance without free oil after 30 minutes at 25 °C, as determined by visual method. Reported median droplet size for self-emulsifying silicone defoamers at 0.1 % dilution under 500 rpm overhead stirring is in the range 1–5 µm; KS-538 plant samples should be verified by ISO 13320:2020 laser diffraction.
Batch release testing for KS-538 includes the following parameters. These values are typical for the product class and should be confirmed against each supplier certificate of analysis.
| Property | Test method | Typical value or range |
|---|---|---|
| Appearance at 25 °C | Visual inspection | White to off-white viscous liquid |
| Nonvolatile content | ASTM D2369-20 | 30.0 ± 2.0 % by mass |
| Viscosity at 25 °C | ASTM D2196-20, Brookfield RV, spindle 4, 20 rpm | 1500–3000 mPa·s |
| Density at 25 °C | ASTM D1475-13 | 0.98–1.02 g/cm³ |
| pH of 1 % dispersion | ASTM E70-19 | 6.5–8.0 |
| Ionic character | Internal method | Nonionic |
For foam control in pigment grinding, the product is typically added at 0.05 to 0.2 mass % based on dry pigment, before the dispersing stage. In latex processing, addition rates of 0.1 to 0.3 mass % are introduced after the pH adjustment step and before vacuum stripping. In styrene-butadiene latex production, defoamer addition must be timed to avoid interference with initiator decomposition; addition before the initiator is not recommended because the product can partition into monomer droplets and alter seed particle formation. Equipment feeding should use positive displacement pumps; centrifugal pumps with high impeller shear can destabilize the self-emulsifying structure and cause silicone oil separation in the dosing line. In wastewater systems, continuous dosing at 1 to 20 ppm active ingredient is common for this defoamer class; actual demand is determined by a sparged foam cell test according to ASTM E2407 with the plant's own process fluid. Overdosing above 50 ppm active can produce haze in treated effluent and reduce oxygen transfer in aeration basins. The product should be drawn from totes with agitator recirculation if stored for more than 7 days; stratification of silicone active and emulsifier may increase batch-to-batch variance in foam control.
Because KS-538 is self-emulsifying, plant installations without rotor-stator mixers can dose the product directly into a flowing water line, provided the line velocity exceeds 1.5 m/s. If the receiving stream is below 1.5 m/s, a static mixer with at least 8 elements is recommended to prevent localized accumulations on tank walls. In contrast, non-self-emulsifying 100 % active silicone compounds require separate high-shear emulsification and can form floating oil lenses if added directly. This difference reduces operator exposure and pre-batch mixing steps. However, the self-emulsifying grade may lose persistency in quiescent systems because the finely dispersed droplets can be solubilized or absorbed onto suspended solids; published data for this specific configuration is limited. In air-washer sumps with low flow, repeated intermittent dosing may be necessary.
The following table summarizes the differentiating characteristics based on supplier technical data and industrial foam-control literature. Where a unit operation has not been validated with KS-538, this is indicated.
| Parameter | KS-538 | Mineral oil defoamer | Polyether defoamer |
|---|---|---|---|
| Active chemistry | Self-emulsifying polydimethylsiloxane | Mineral oil and hydrophobic silica | EO/PO block copolymer |
| Dispersibility in water at 25 °C | Spontaneous milky dispersion under mild agitation | Requires surfactant or high shear; may form macroemulsion | Water-soluble; may form clear solution |
| Typical addition rate in latex | 0.1–0.3 mass % | 0.2–0.5 mass % | 0.3–0.8 mass % |
| Persistence in agitated reactors | High, but shear dependent | Moderate; can separate at high temperature | Low to moderate; removed with foamate |
| Surface haze risk in clear coatings | Low at low dose | Moderate; oil migration possible | Low |
| Emulsion stability pH window | 4–11 | 4–10 | 2–13 |
In clear coating formulations, mineral oil defoamers can migrate to the air–coating interface and cause surface defects; KS-538 disperses into the aqueous phase and is less likely to form persistent oil lenses at use levels below 0.1 mass %. In contrast, polyether defoamers may remain soluble in the continuous phase and can produce lower initial foam knockdown in surfactant-rich systems. Selection among these chemistries is therefore governed by the maximum allowable surface haze, the required foam decay time, and the process temperature. For KS-538, the reported emulsion stability pH window is 4–11; outside this range, the use of a process-compatible polyether defoamer may be necessary. The self-emulsifying grade is supplied at 30 % nonvolatile content, which is lower than 100 % active silicone compounds; therefore higher dosage volumes are required to deliver equivalent active silicone. This lower active content improves ease of dispersion but increases freight and storage volume per unit of active silicone.
Storage below 5 °C should be avoided; freeze-thaw cycling can cremate the internal emulsifier and increase viscosity beyond pumpable limits. If frozen, the material must be warmed to 25 °C and gently agitated for 1 hour, but emulsion integrity is not guaranteed. Avoid contact with strong oxidizers such as sodium hypochlorite; undiluted mixing with hypochlorite may generate local exothermic reactions. In papermaking, retention of this product in finished sheet must be considered under 21 CFR 176.210 if food-contact use is intended; no claim of compliance applies without full supplier documentation. Compliance with REACH Regulation (EC) No 1907/2006 and RoHS Directive 2011/65/EU applies to the product as supplied, not to diluted downstream formulations.
In cooling water circuits, continuous dosing is typically introduced after the heat exchanger return line. Addition before the heat exchanger is not recommended because thermal degradation of the silicone active at tube skin temperatures above 120 °C may occur. In paper coating, the product is injected after the machine screen and before the coater feed tank to reduce air bubbles and improve blade coater runnability; addition before pressure screens may result in retention of active silicone and reduced foam knockdown. The product should be added downstream of fine filters where possible, because repeated passage through 10 µm bag filters can remove active silicone droplets and reduce foam-control efficiency.
Before plant-wide use, a side-stream trial is recommended. For paper coating, a laboratory pulper can simulate addition and measure air content using a density method; a side-stream coating pan trial can validate absence of fisheye formation. In cooling towers, a two-week trial with continuous dosing at 5 ppm active is used to monitor foam height in the tower basin and drift eliminator blockage. The product should be evaluated under actual pH, temperature, and filtration shear; published data for other equipment configurations cannot substitute for site-specific validation. This product is not recommended for mineral flotation circuits, because silicone defoamers can suppress froth recovery of mineral particles.