| HS Code | 455504 |
| Productname | KM-71 General Industrial Silicone Antifoam Emulsion |
| Producttype | General-purpose silicone antifoam emulsion |
| Ioniccharacter | Nonionic |
| Appearance | Milky white liquid |
| Nonvolatilecontent | 30% |
| Specificgravityat25c | 1.00 |
| Viscosityat25c | 1000 mPa·s |
| Phat25c | 6.0 |
| Watersolubility | Dispersible in water |
| Dilutionstability | Stable upon dilution with water |
| Phstabilityrange | 4-10 |
| Storagestability | 6 months when stored at 5-35°C |
| Freezethawstability | Protect from freezing |
As an accredited KM-71 General Industrial Silicone Antifoam Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | KM-71 silicone antifoam emulsion is supplied in sealed containers, available in 25 kg pails, 200 kg drums, or 1,000 kg bulk totes. |
| Container Loading (20′ FCL) | One 20′ FCL container loading of KM-71 silicone antifoam emulsion in drums/IBCs, secured safely, non-hazardous general cargo for shipment. |
| Shipping | KM-71 Silicone Antifoam Emulsion ships in sealed drums, pails, or totes, depending on volume. Protect from extreme heat and freezing during transit. Ensure containers remain upright and securely palletized. Generally non-hazardous, but avoid spills and follow standard industrial chemical handling and disposal guidelines. |
| Storage | Store KM-71 in its original, tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Protect from freezing and temperatures above 40°C (104°F). Keep containers upright and clearly labeled. Avoid contact with strong oxidizers. Ensure spill containment and proper secondary containment where required. |
| Shelf Life | Shelf life is typically six months from manufacture when stored in original unopened containers at recommended temperatures; avoid freezing. |
In open recirculating cooling water systems where nonionic polymeric dispersants and phosphate-based scale inhibitors are dosed at 10–20 mg/L as active solids, foam stabilisation occurs when entrained air is retained by a surface-active film of organic contaminants, glycol by-products or tallow-based corrosion inhibitors. KM-71, a general industrial silicone antifoam emulsion, is applied to break such films at continuous addition rates of 5–50 ppm relative to circulating water volume. The product should be metered neat or after 1:9 dilution with demineralised water using a positive-displacement peristaltic pump set to 1–3 L/h, with injection into the cooling tower basin return line at a point 0.5–2 m upstream of the basin inlet to avoid pump suction air entrainment. During foaming upsets caused by heavy biological slough or surfactant carryover, a slug dose of 100–200 ppm over 15–30 minutes can be introduced through a separate chemical injection quill; however, total residual silicone above 200 ppm is not recommended because plate heat exchangers with narrow 3–5 mm channels and downstream 5–25 µm cartridge filters can accumulate hydrophobic deposits that reduce heat transfer coefficients by 15–30 % and increase pressure differential across the filter bank. Free chlorine or bromine residuals above 5 mg/L should be avoided at the point of injection because oxidising biocides can destabilise the emulsion droplet, phase-separate the silicone oil, and generate floating oil films in the basin. The treated water is then returned to process heat exchangers, evaporative condensers and scrubber systems as a low-foam circulating medium, with foam knockdown evaluated by ASTM E2407 using 100 mL sample volumes at 25 °C; a 150 mL graduated cylinder foam height of less than 10 mL after 5 minutes is typically considered acceptable for cooling tower basin control, though product-specific data for KM-71 should be confirmed against the plant-specific water matrix.
Field observations on induced-draft crossflow towers with 0.5–1.0 m³/h per m² water loading indicate that dosing below 5 ppm results in a nonlinear return of foam within 4–6 hours when saponified organic fouling is present, whereas dosing above 50 ppm increases the risk of visible slicks on hot-deck distribution pans. Emulsion stability in plant water containing 200–800 ppm total dissolved solids and 100–300 ppm calcium hardness as CaCO3 should be checked by adding 1 mL of the product to 100 mL of plant water in a stoppered cylinder; phase separation greater than 2 mL after 24 hours at 25 °C indicates that a softened water predilution line is required. On units with automatic foam sensing by ultrasonic level transmitters, the control loop is typically configured with a 15-minute on-off delay to avoid pump short-cycling and silicone overfeed during normal turbulent basin return.
High-solids styrene-acrylic and vinyl acetate-ethylene binders with associative polyurethane thickeners produce persistent foam when dispersing wetting agents and coalescing solvents lower dynamic surface tension below 32 mN/m at 25 °C. KM-71 is incorporated at 0.05–0.30 wt% of total formulation mass, with the lower end reserved for flat interior wall paints and the upper end for elastomeric roof coatings and high-PVC textured finishes. The standard addition point is the letdown vessel after the pigment grind is cooled below 40 °C and before the final rheology modifier solution is added. A disc disperser with a tip speed of 4–6 m/s is held for 10–15 minutes; prolonged shear above 30 minutes or repeated passes through an in-line rotor-stator mixer can rupture the polydimethylsiloxane droplets, increasing surface defect formation because coalesced micro-droplets rise to the wet film surface before film coalescence is complete. Reverse addition into the grind phase with high free-surfactant content should be avoided because the silicone may adsorb onto dispersed pigment surfaces and lose interfacial mobility. The resulting latex paints, plasters and roof coatings are tested for foam control using a reciprocating shaker; a 200 mL sample shaken for 60 seconds should settle to less than 50 mL foam height within 5 minutes. Regulatory status is governed by US EPA Method 24 for VOC, EU Directive 2004/42/EC Decopaint for architectural product subcategories, and REACH Annex XVII restrictions for cyclic siloxane content if D4/D5/D6 levels exceed 0.1 % by weight in the final formula.
| KM-71 addition (wt%) | Initial foam after 60 s (mL) | Foam after 5 min (mL) | Surface defect observation |
|---|---|---|---|
| 0 | 180 | 140 | Uniform microbubble veil |
| 0.05 | 60 | 20 | None |
| 0.10 | 45 | 10 | None |
| 0.20 | 30 | 5 | None |
| 0.30 | 25 | 5 | Three craters per 0.5 m² panel after 7 days |
This screening matrix is a formulation development framework rather than a commercial specification; the surface defect threshold varies with binder hardness, coalescent type and film thickness, and a final drawdown panel must be evaluated under DIN EN ISO 2813 gloss conditions to separate micro-cratering from incidental dust contamination.
During high-shear bead milling of 480 g/L chlorothalonil suspension concentrates and 40 % emulsifiable concentrates formulated with calcium dodecylbenzene sulfonate and tallow amine ethoxylates, air entrainment becomes severe when wetting agent concentrations exceed 20 g/L in the slurry phase. KM-71 is introduced as an in-can antifoam at 0.05–0.30 % w/w on total formulation weight, preferably after the dispersing agents have been dissolved but before the technical active is drawn into the dispersion tank, so that the silicone droplets are distributed through the continuous phase without being destroyed by dry pigment agglomerates. For formulations using a horizontal bead mill with 0.8–1.2 mm zirconia beads and a tip speed of 10–14 m/s, the emulsion should be added as a 1:5 predilution in glycol or water to reduce localised viscosity shock; post-milling addition is reserved for trace corrective dosing because it can leave silicone droplets on the mill screen and produce pinhole defects in water-dispersible granule extrusion. The terminal suspension concentrates, suspo-emulsion formulations and emulsions-in-water are subsequently evaluated by CIPAC MT 47.2 for persistent foam after shaking, and the defoaming agent must not depress wet sieve retention below 98 % on a 75 µm sieve. Compliance with FAO/WHO specifications for pesticide formulations is relevant only when the final product is labelled for public procurement under those specifications; otherwise REACH Annex II safety data sheet reporting applies for the silicone emulsion itself. At pH below 4 or above 10, emulsion stability is tested for 14 days at 54 °C, and separation greater than 5 % by volume invalidates in-can use.
In-can performance does not automatically translate to spray-tank foam suppression at farm dilution because the emulsion concentration drops below the critical coalescing threshold. A 0.2 % w/w loading in a 500 g/L SC produces a use-dilution silicone concentration of 20 ppm at a 1:100 spray-tank dilution; spray tank foam rarely requires additional defoamer when the formulation pseudoplasticity index is below 0.4. If foam persists in a knapsack or vehicle-mounted sprayer, a separate tank-mix antifoam addition at 10–50 mL/hL is used rather than increasing in-can KM-71 loading, because overdosing during formulation causes particle size growth of the suspended active and changes suspensibility after 2-year storage.
Saponified resin acid soaps and sodium lignosulfonates in weak black liquor produce persistent foam that reduces vacuum drum washer throughput when liquor solids exceed 15 % and residual effective alkali is above 8 g/L as Na2O. KM-71 is applied at 0.02–0.10 % based on dry fiber mass or 50–300 g per tonne of black liquor solids, with the exact dose set by washer foam height and entrained air measured by density loss in the filtrate tank. The preferred addition point is the filtrate tank or shower water header where the product is prediluted at 1:10 with warm water at 40–50 °C before contacting 80–95 °C black liquor; direct injection into the blow tank without dilution can cause shock emulsion breakdown at pH 12.0–13.5. A progressive cavity pump is preferred over centrifugal transfer because low-shear metering preserves the silicone emulsion's dispersed phase. In systems with pressure knotters or thickened final screens, residual antifoam may form deposits on polypropylene felt if the addition exceeds 0.15 % of dry fiber; acceptance tests on washer shower nozzles should include a 24-hour continuous trial with differential pressure logging across the first-stage filtrate screen. The resulting unbleached softwood kraft pulp and linerboard stock are governed by 21 CFR 176.210 for defoaming agents used in paper and paperboard intended for food contact, provided the silicone content in the finished board does not exceed the regulation's purity constraints.
Vacuum drum washer air leaks and shower nozzle plugging are the two most common failure modes when defoamer dosage is increased beyond the required threshold. A 0.10 % dry-fiber addition can raise first-stage vacuum from 20–25 kPa to 45–55 kPa in a three-stage countercurrent washing line, but it can also reduce filtrate density if the defoamer accumulates in the recovered soap skimmings. Mill performance is therefore determined by measuring sodium loss from the pulp mat after the third washer, with a target below 2.5 kg Na2SO4 per tonne of pulp, and by maintaining foam height in the filtrate tank below 0.5 m.
| Condition | Standard or regulatory designation | Verify |
|---|---|---|
| Food-contact defoamer in paper and paperboard | 21 CFR 176.210 | Silicone purity and addition mass |
| Kraft mill effluent limitations | 40 CFR Part 430 | BOD, TSS, pH discharge permit |
| EU packaging food contact | Regulation (EC) No 1935/2004 | Overall migration |
Centralised semisynthetic metalworking fluid systems at 7–10 % concentration in 200–400 L sumps develop foam carryover when high-pressure through-tool coolant delivery returns air from mist collection and entrained tramp oil rises above 2 % by volume. KM-71 is added either to the concentrate during blending at 0.05–0.25 wt% or as a tank-side post-dose at 50–200 ppm based on the circulating charge, using a drop-feed over 30–60 minutes rather than a single pour to prevent surface film formation on the skimmer belt and level sensors. Mechanical filtration with 10–25 µm bag filters and high-speed spindle through-tool passages above 40 bar can strip silicone droplets from the aqueous phase; therefore, post-filter injection points or split dosing is required on systems where filter changeout intervals are shorter than 8 hours. The water phase should be maintained at pH 8.5–9.5 and total hardness below 500 ppm as CaCO3 to minimise calcium soap interaction with emulsion destabilisers. Foam persistence is evaluated by ASTM D3601 at 25 °C and 5 minutes of air diffusion, with acceptance criteria set at less than 50 mL stable foam after 10 minutes of settling. The terminal semisynthetic metalworking fluid is used for face milling, thread cutting and cylindrical grinding; compatibility with quaternary ammonium and triazine biocides should be confirmed in a 7-day storage test at 40 °C before central system release.
Field batch variance in metalworking fluid concentrate blending is commonly caused by incomplete antifoam dispersion when the high-pH amine base is charged before the oil phase. A reverse-addition sequence, in which KM-71 is mixed into the oil phase before the alkanolamine neutraliser, provides better emulsion stability than post-neutralisation addition because the silicone droplets are shielded from high local pH gradients that can exceed 11.0 at the amine inlet.
Jet dyeing machines operating at 1:6–1:8 liquor ratios and 300–600 m/min fabric rope speeds generate foam in the sump when disperse dye carriers, leveling agents and alkali are charged into polyester-cotton blends. KM-71 is dosed at 0.1–0.3 g/L of bath volume, prediluted 1:5 with 30–35 °C demineralised water, and injected after sequestrants but before the dye addition, with half of the total charge at bath preparation and half after 30 minutes of circulation to compensate for shear-induced emulsion droplet rupture in venturi nozzles. The end products—dyed knit or woven polyester-cotton fabric—are finished under conditions where residual silicone antifoam at bath exhaustion must not interfere with subsequent wicking or coating; a cold pad-batch test for water absorbency is performed after dyeing. ZDHC MRSL v3.1 compliance applies only if the dyehouse effluent is discharged through a registered wastewater treatment plant; the silicone emulsion itself must not contain intentionally added APEO, and proof is maintained through a supplier certificate of analysis showing non-detectable levels at a reporting limit of 10 mg/kg.
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KM-71 General Industrial Silicone Antifoam Emulsion is a water-dilutable, nonionic oil-in-water dispersion whose active foam-control components are a high-viscosity dimethylpolysiloxane fluid and a hydrophobized silica network. Manufacturer-published representative values for the as-supplied product are listed in Table 1. The nonvolatile matter is 30 ± 1% by mass, pH is 6.5–8.0 as supplied, specific gravity is 0.99–1.01 at 25 °C, and Brookfield LVT viscosity is 1500–3500 mPa·s at 25 °C using spindle 2 at 30 rpm. The product appears as a milky white liquid that may cream on standing and must be remixed with a low-shear paddle before use. The silicone phase lowers the air–water interfacial tension to approximately 21 mN/m, which permits rapid spreading across foam lamellae, film thinning, and bubble coalescence. The product is a general industrial grade and is not sold under 21 CFR 173.340 clearance for direct food-contact use.
| Property | Typical value | Test procedure |
|---|---|---|
| Appearance | Milky white emulsion | Visual inspection of a sealed container at 20–25 °C |
| Nonvolatile matter | 30 ± 1% by mass | ISO 3251, oven method at 105 °C for 3 h |
| pH as supplied | 6.5–8.0 | ISO 4316 with glass electrode at 25 °C |
| Specific gravity | 0.99–1.01 | ISO 2811-1 pycnometer method at 25 °C |
| Viscosity | 1500–3500 mPa·s | Brookfield LVT, spindle 2, 30 rpm, 25 °C |
| Ionic character | Nonionic | Emulsifier type determination |
| Continuous phase | Water | Composition |
Because the emulsion is nonionic, it can be incorporated into many anionic and nonionic processing formulas without charge-driven coagulation, but concentrated cationic coagulants can heterocoagulate with the emulsifier layer and should not be mixed directly with the undiluted product. Foam-control behavior is not a single physical property but a combination of spreading, dewetting, and particle-bridge rupture. The hydrophobic silica particles create a three-phase contact angle that is irreversible in many foam films, allowing the emulsion to function as both a knock-down defoamer and a persistent antifoam. The required addition rate therefore depends on the foam age, the surfactant type, the presence of suspended solids, and the process shear history.
Addition of KM-71 to a process stream is normally performed by continuous metering or by slug addition at the point of foam generation. Effective as-supplied addition levels in aqueous systems are typically 10–500 ppm; however, field determination by jar or bottle test according to ASTM D3601 is required because no single dosage is valid across all foam systems. A screening protocol uses air flow of 0.1 L/min through 200 mL of foaming liquid at 25 °C, with foam height recorded after 5 min. In production-scale agitated reactors, the emulsion should be injected into a high-turbulence zone such as the impeller discharge or an eductor loop, not directly into the vortex of a high-shear rotor-stator mixer. High-shear dispersion can reduce the droplet size of the emulsion and lower long-term antifoam persistence, although the initial knock-down speed may appear improved.
Mineral oil-based defoamers are usually formulated with hydrophobic wax particles dispersed in a low-viscosity mineral oil and are commonly applied at 100–2000 ppm. Their performance falls off when process temperature exceeds 60–80 °C because the oil viscosity drops and the wax particles may dissolve or settle. Polyether polyol defoamers offer better compatibility in clear coatings and metalworking fluids, but they typically show lower knock-down at low addition rates and have an active thermal limit near 50–70 °C. KM-71 differs in that the active polydimethylsiloxane fluid remains thermally stable to approximately 200 °C in bulk and exhibits very low vapor pressure, making it suitable for vacuum processes and hot distillation where solvent-based defoamers would volatilize. The aqueous emulsion form, however, is not the same as the bulk fluid; continuous process exposure above 90 °C at atmospheric pressure or above 60 °C in high-electrolyte solutions should be validated because the emulsifier layer may dehydrate and allow droplet coalescence.
Compared with low-solids silicone emulsions containing 10–20% nonvolatile matter, KM-71 at 30% nonvolatile matter reduces freight and storage volume but is more concentrated and should be prediluted before dosing into small-volume processes. Compared with solvent-containing silicone antifoams, KM-71 uses water as the continuous phase and therefore avoids volatile organic compound introduction in many applications. A dilution ratio of 1:10 to 1:100 with water at 20–30 °C is typical; the emulsion is added to the water under gentle agitation at 100–300 rpm. Diluted material should be consumed within 24 h because the dilution may support microbial growth and lose stability. The diluted emulsion should be visually inspected after 1 h; formation of an oily surface layer or large floccules indicates incompatibility with process water hardness, pH, or electrolyte concentration.
| Property | KM-71 silicone emulsion | Mineral oil/wax defoamer | Polyether polyol defoamer |
|---|---|---|---|
| Active foam-control chemistry | Dimethylpolysiloxane fluid with hydrophobized silica network | Mineral oil with hydrophobic wax particles | EO/PO block copolymer |
| Typical as-supplied dose in aqueous foam | 10–500 ppm | 100–2000 ppm | 50–1000 ppm |
| Bulk thermal limit of active component | 200 °C | 60–80 °C | 50–70 °C |
| Air–water surface tension | ~21 mN/m | 30–35 mN/m | 28–33 mN/m |
| Emulsion service pH window | 4–10 short term | 4–12 | 3–11 |
| Risk in clear coatings above critical dose | Craters and fish eyes above 0.7% addition | Oil separation and loss of gloss | Lower risk; may reduce block resistance |
| Wastewater nonvolatile contribution | Low but measurable at high dose | Can increase COD/BOD significantly | Moderate and partially biodegradable |
Foam in distillation columns and vacuum strippers increases tray pressure drop, reduces separation efficiency, and can carry nonvolatile contaminants into overhead condensers. KM-71 is injected upstream of the feed preheater or directly into the column sump at rates from 20 ppm to 200 ppm relative to total feed. In a vacuum stripping column operating at 50 kPa absolute, the low vapor pressure of the silicone active fluid minimizes distillate contamination, which is a key difference from solvent-based antifoams. Overdosing, however, can create a stable oil-in-water dispersion in the column bottoms and reduce vapor–liquid mass transfer by blanketing the interface. The addition rate should be increased stepwise while monitoring differential pressure across the first tray section; a drop of more than 15% from baseline following addition may indicate that the antifoam is suppressing foam but is approaching hydraulic instability, and the dose should be reduced until tray efficiency and pressure drop stabilize. Published data for KM-71 in all possible solvent-rich distillation configurations is limited, so pilot-tower verification with the actual feed matrix is necessary for high-value separations.
In black liquor evaporation and alkaline pulp processes, silicone antifoam emulsions are generally preferred over oil-based defoamers because of thermal stability and lower pitch contribution. KM-71 may be added at the recirculation pump discharge; however, black liquor pH often exceeds 12 and dissolved solids may exceed 60% in the effects, conditions that can destabilize a general industrial emulsion. Compatibility with the specific black liquor solids and temperature should be confirmed by a settling test at 80 °C before continuous use. If phase separation or oiling occurs within 30 min, a dedicated high-alkaline silicone grade or a silicone compound may be required.
Activated sludge aeration basins and industrial effluent channels usually require KM-71 at 10–300 ppm relative to feed flow. Field observations from municipal and industrial effluent plants indicate that addition at the aerator outlet weir rather than the inlet channel reduces defoamer recirculation through the aeration grid and improves knock-down persistence. Operators should monitor foam height with a calibrated staff gauge and adjust dosing to maintain a foam collar below 10 cm at the basin perimeter; published data for specific activated sludge configurations is limited, so dose titration remains mandatory. A 30% nonvolatile emulsion added at 100 ppm contributes approximately 30 ppm nonvolatile organic mass to the effluent stream, which must be considered in discharge permit calculations even though the silicone polymer itself has low oxygen demand. If downstream reverse osmosis or ultrafiltration is used, residual silicone may foul membranes; the minimum effective dose should be maintained and permeate flux should be trended.
Waterborne coating letdown and emulsion polymerization processes use KM-71 to suppress microfoam generated by pigment dispersion and high-speed filling. Addition is typically 0.05–0.5% by formulation mass. Above 0.7%, silicone migration to the drying film may create craters, fish eyes, and loss of intercoat adhesion. Drawdown leveling should be checked according to ASTM D4062 or an equivalent flow/leveling method before production use. In a 20 m³ batch polymerization reactor equipped with a pitched-blade turbine at 1.5 m/s tip speed, addition of KM-71 at the monomer feed nozzle can control foam during the early exotherm without retarding polymerization. However, the product should be evaluated for monomer conversion and particle size distribution at the target dose because silicone droplets can associate with polymer particles and alter particle nucleation if added during the nucleation stage.
KM-71 is not recommended for continuous operation in strongly acidic or strongly alkaline streams outside a pH range of 4–10 unless emulsion stability is revalidated at the process temperature. It is not suitable for direct food-contact applications unless a food-grade silicone antifoam cleared under 21 CFR 173.340 is selected. It should not be used in closed-loop cooling water treated with high concentrations of ozone or chlorine dioxide, because oxidative attack on the emulsifier layer may reduce dispersion stability. It is also not recommended for systems that require absolutely no silicone deposition on downstream membranes, sensors, or optical surfaces; in those cases, a non-silicone defoamer or a process redesign may be necessary. Safety data sheets prepared under the CLP Regulation (EC) No 1272/2008 should be consulted for hazard classification, and REACH registration status under Regulation (EC) No 1907/2006 should be verified for the specific import lot.
Store KM-71 in sealed containers at 5–35 °C and protect from freezing. If freezing occurs, thaw at 20–25 °C for 24 h and remix with a low-shear paddle. A single freeze-thaw cycle may not restore the original particle size distribution, and the material should be re-evaluated by a bottle test according to ASTM D3601 before use. Positive displacement metering pumps with EPDM or Viton elastomer seals are preferred; silicone rubber tubing is not recommended because it can swell in contact with the silicone phase. Injection should be located downstream of a static mixer or at the impeller discharge of an agitated vessel. Do not inject undiluted KM-71 into the suction side of a centrifugal pump where localized vacuum and high shear may destabilize the emulsion and reduce foam-control persistence. If the product is stored beyond 12 months, pH and viscosity should be rechecked; a pH shift greater than 0.5 or a viscosity drift greater than ±15% from the original lot value may indicate incipient destabilization.
In jet dyeing of polyester and cotton blends, foam in the circulation pump can cause pump cavitation and uneven dye uptake. KM-71 is dosed at 0.1–0.5 g/L in the dyebath, but compatibility with disperse dyes and leveling agents should be confirmed by a cup test under production pH and temperature. In alkaline soak cleaning tanks for metal finishing, rates from 20 ppm to 100 ppm are typically sufficient to control foam at 60 °C, but the emulsion should be added to a well-agitated zone to avoid localized oiling. Because residual silicone can affect subsequent plating or coating adhesion, parts should be rinsed according to the existing process sequence, and the final rinse should be monitored for water-break-free surfaces.