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KS-7709 MXHF-Solution Silicone Defoamer

    • Product Name: KS-7709 MXHF-Solution Silicone Defoamer
    • 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 200932
    Product Name KS-7709 MXHF-Solution Silicone Defoamer
    Appearance Milky white viscous liquid
    Active Silicone Content 30%
    Viscosity 25 C 500-1500 mPa·s
    Ph 1 Aqueous Solution 6.0-8.0
    Specific Gravity 25 C 1.00-1.05
    Ionic Type Non-ionic
    Water Dispersibility Easily dispersible in water
    Defoaming Efficiency High
    Foam Suppression Duration Long lasting
    Storage Stability Stable for 12 months under normal conditions
    Temperature Resistance 0°C to 100°C
    Freezing Point 0°C, may freeze but remains effective after thawing and mixing

    As an accredited KS-7709 MXHF-Solution Silicone Defoamer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing KS-7709 MXHF-Solution Silicone Defoamer is supplied in 25 kg / 200 kg drums, sealed for safe storage and transport.
    Container Loading (20′ FCL) 20′ FCL container loaded with KS-7709 MXHF-Solution Silicone Defoamer, safely packed, secured, and documented for transport.
    Shipping KS-7709 MXHF-Solution Silicone Defoamer ships in sealed drums, totes, or custom packaging. Classified as non-hazardous cargo under normal conditions. Protect from freezing, direct sunlight, and moisture. Use covered, ventilated transport. Keep containers upright and secured to prevent leakage during transit.
    Storage Store KS-7709 MXHF-Solution Silicone Defoamer in a cool, dry, well-ventilated area away from direct sunlight, heat, and freezing conditions. Keep the container tightly sealed when not in use to prevent contamination or evaporation. Avoid storage near strong oxidizing agents or incompatibles. Maintain temperature between 5–35°C; under proper conditions, shelf life is typically 12 months.
    Shelf Life Shelf life is 12 months from manufacture date when stored in original, unopened containers at recommended temperatures, away from freezing and direct sunlight.
    Application of KS-7709 MXHF-Solution Silicone Defoamer

    In waterborne acrylic and acrylate-styrene architectural coatings, KS-7709 MXHF-Solution Silicone Defoamer is introduced after the letdown stage to eliminate macrofoam generated by associative polyurethane thickeners and by Cowles blade dispersion at tip speeds of 2 m/s to 4 m/s. Addition levels of 0.10 wt% to 0.40 wt% based on total formulation weight are normal; in semigloss and high-gloss systems with ASTM D523 gloss readings above 80 GU at 60°, the preferred band is 0.10 wt% to 0.20 wt% to prevent surface haze and loss of distinctness of image. The downstream production process is a high-speed dispersion line in which pigment slurry is ground to a Hegman gauge reading of 5 to 6 before letdown, and the defoamer is added at 20 rpm to 40 rpm slow-speed mixing for not less than 15 minutes. Terminal finished product types include interior and exterior latex wall paints, waterborne wood primers, elastomeric roof coatings, and waterborne anti-corrosion topcoats. Compliance for this segment uses ASTM D3960-16 for VOC content, GB 18582-2020 for hazardous substance limits in interior wall coatings, and FDA 21 CFR 176.200 when coating components or defoaming agents are used in food-contact can coatings. Over-dosing above 0.50 wt% tends to reduce intercoat adhesion, and post-addition shear above 1 500 rpm may destabilize the silicone-hydrophobic silica droplets and create cratering.

    In 1 000 L production tanks with radial impellers, macrofoam height can shift level-sensor readings by 2% to 5% of batch volume when associative thickener solution is charged too rapidly, so the defoamer is dosed before final rheology adjustment and not after, to prevent air incorporation during the final viscosity plateau. A foam-control screening method based on ASTM D3601 is used to compare the formulation before and after addition; the defoamer is considered acceptable when foam height returns to a stable plateau at least 20% lower than the control at the same mixing input.

    What Limits Defoamer Retention in Aerobic Fermentation Broths with Silicone Droplet Diameters of 10–50 µm?

    Aerobic fermentation broth foam height is governed by gas hold-up, superficial air velocity of 0.5 vvm to 2.0 vvm, and the concentration of extracellular protein at the broth surface; KS-7709 MXHF-Solution Silicone Defoamer is metered as a sterile diluted feed to maintain a headspace foam layer below the outlet filter plane. Addition ratios for fungal, bacterial, and yeast broths typically fall between 0.01 v/v% and 0.05 v/v% of initial working volume, with split dosing every 60 minutes to 120 minutes rather than single-shot application. In a production stirred tank of 5 m3 to 200 m3 with two Rushton impellers, the defoamer is delivered through the sterile feed line after 121 °C autoclaving for 30 minutes; injection into the top-sweep zone above the liquid surface is preferred when mechanical foam breaker torque exceeds set-point. Terminal finished product types include citric acid, lactic acid, amino acids, enzymes, and bioethanol. Compliance with FDA 21 CFR 173.340 applies when the defoamer is used in food-grade fermentation; in EU-regulated food processing, dimethylpolysiloxane as an antifoaming agent is controlled by Regulation (EC) No 1333/2008 under E 900. Over-addition above 0.10 v/v% has been associated with a measurable decline in oxygen transfer coefficient kLa in filamentous fungal broths because the defoamer film restricts interfacial renewal at the air-water boundary.

    On production-scale airlift reactors, foam carryover into the exhaust condenser can reduce cooling capacity and raise back-pressure on the sparge line by 0.3 bar to 0.8 bar within 2 hours if untreated; the defoamer is therefore injected through the top-foam zone at 0.005 v/v% increments until condenser pressure drop returns to baseline. A downstream harvesting bottleneck is the persistence of defoamer droplets in the broth; if cell separation is performed by tangential flow filtration with 50 kDa to 500 kDa membranes, excess silicone can coat the membrane surface and reduce flux, so the lower addition band is validated against normalized permeate flux.

    When Jet Dyeing Machine Ramp-Up Exceeds 300 m/min, Foam Collapse Must Be Managed in the Dye Bath

    Synthetic and cellulosic dyeing lines operating at fabric rope speeds of 300 m/min to 700 m/min entrain air in the venturi and main circulation pump, producing foam that cavitates pumps and creates uneven dye uptake on polyester-cotton knits. KS-7709 MXHF-Solution Silicone Defoamer is pre-diluted with 5 parts of water and added to the dye bath at 0.05 g/L to 0.20 g/L before the temperature ramp-up toward 130 °C to 135 °C. The downstream production process is a high-temperature exhaust dyeing process at a liquor ratio of 5:1 to 8:1, with chemical injection through a dosing tank and a bath circulation cycle of 2 minutes to 4 minutes per turn. Terminal finished product types include dyed polyester-cotton interlock, nylon-spandex warp knits, cotton terry toweling, and automotive upholstery fabrics. Compliance relevant to this segment includes OEKO-TEX Standard 100 for fabric residues, ZDHC MRSL v3.1 restrictions on cyclic siloxanes D4, D5, and D6 at 0.1 wt% each, and REACH Annex XVII for chemical safety. Because silicone defoamer droplets can deposit hydrophobic spots on high-filament-count nylon if bath circulation drops below 1 minute/turn, the feeding is performed under maximum pump flow and the bath is sampled for oil-spot formation before dye liquor is discharged.

    On production beam dyeing machines with liquor ratios below 5:1, the defoamer is added only after the wetting agent has fully dissolved because simultaneous injection with concentrated surfactant can form a persistent oil-in-water emulsion that deposits on guide rolls. During reduction clearing, residual sodium hydrosulfite at 3 g/L to 5 g/L regenerates foam from residual surfactant, so an additional 0.03 g/L to 0.05 g/L defoamer is introduced before the clearing bath is heated.

    In alkaline fine paper and packaging board machine wet ends running with 40% to 80% whitewater closure, dispersed air entering through high-consistency stock pumps and centrifugal cleaners produces sheet holes and retention aid interference, and KS-7709 MXHF-Solution Silicone Defoamer is injected at the fan pump suction or headbox approach before the slice. The addition ratio ranges from 0.2 kg/t to 0.6 kg/t of bone-dry fiber, with tissue machines at the lower band 0.1 kg/t to 0.3 kg/t due to wet strength additive sensitivity. Downstream production is a continuous fourdrinier or gap former at machine speeds of 600 m/min to 1 200 m/min, where the defoamer is metered into the whitewater tray and the mixed flow passes through a fan pump and pressure screen before the headbox; the target is to reduce dissolved air below 0.5% by volume to prevent pinholes in lightweight linerboard. Terminal finished product types include tissue, fluting medium, testliner, and silicone-coated release paper base. Compliance for food-contact paper and board is anchored to FDA 21 CFR 176.210, and European mills typically verify defoamer components against BfR Recommendation XXXVI; published head-to-head dosing studies for this exact product code in closed whitewater loops are limited, so the upper addition rate should be validated against first-pass retention and sheet wet strength variation. Over-dosing above 0.8 kg/t may create pitch-like deposits on ceramic forming fabric and reduce the efficiency of cationic retention aids.

    A specific operational boundary occurs during grade changes from unbleached linerboard to white top liner, where the wet end temperature can shift by 10 °C to 20 °C within 30 minutes; the defoamer feed should be recalibrated to the new temperature because solubility of air in whitewater is inversely related to temperature. Mills using gap formers at speeds above 900 m/min have reported foam-induced basis weight variation of 0.5 g/m2 to 1.5 g/m2 when the defoamer pump loses prime, which demonstrates the need for continuous metering rather than pulsed addition into the fan pump suction.

    Where Low-Foam Surfactant Packages Fail under High-Pressure CIP Recirculation

    Industrial and institutional cleaning concentrates based on nonionic alkoxylate packages exhibit foam rise at recirculation pressures of 5 bar to 10 bar in clean-in-place systems, and KS-7709 MXHF-Solution Silicone Defoamer is included to suppress this foam during dilution to 1% to 5% use solutions. The formulation addition ratio is 0.05 wt% to 0.30 wt% in the concentrate, added after neutralization when the batch temperature is below 40 °C; lower levels are effective in low-electrolyte formulas, while higher levels are required in concentrated alkaline systems with caustic content above 10 wt%. Production is a batch mixing process using pitched-blade turbines at 20 rpm to 40 rpm, where the defoamer is incorporated before final viscosity adjustment to ensure no separation during storage. Terminal finished products include CIP detergents for dairy and beverage plants, high-alkali floor degreasers, and transport wash detergents. Compliance is evaluated under EU Detergent Regulation (EC) No 648/2004 and foam behavior by ASTM D3601; silicone defoamer levels must not mask the primary surfactant foam profile under ASTM D1173 for hand dishwashing detergents, so application is confined to low-foam industrial cleaning formulations.

    Can Suspension Concentrate Milling Stabilize Against Microfoam while Maintaining CIPAC MT 47.2 Limits?

    High-gravity pesticide suspension concentrates with solids fractions of 450 g/L to 650 g/L entrain microfoam during horizontal bead milling with 0.6 mm to 1.0 mm zirconia beads, and foam collapse must occur before CIPAC MT 47.2 measurement of persistent foam after 60 seconds settling. KS-7709 MXHF-Solution Silicone Defoamer is added at 0.1 wt% to 0.4 wt% of the formulation, often as a split addition: 0.05 wt% before milling to reduce mill packing and 0.15 wt% to 0.25 wt% after milling with low-shear agitation. The downstream production process is a wet grinding and high-shear homogenization line in which mill-base temperature is controlled at 35 °C to 45 °C, followed by deaeration under vacuum of 0.08 MPa to 0.09 MPa. Terminal finished product types include herbicide, fungicide, and insecticide suspension concentrates plus oil dispersion formulations. Compliance frameworks include FAO/WHO Manual for Development and Use of FAO/WHO Specifications for Pesticides, CIPAC MT 47.2 for persistent foam, and EPA 40 CFR 180.910 for inert ingredients used in formulations for crop use; for EU authorization under Regulation (EC) No 1107/2009, formulation toxicology and residue data may be required when the formulation is placed on food crops.

    On horizontal bead mills with chamber volumes of 10 L to 100 L, microfoam becomes visible as mill discharge density drops by 50 g/L to 100 g/L against the target batch density; this condition also raises outlet temperature by 2 °C to 4 °C due to reduced heat transfer. The defoamer is therefore monitored by density and foam height, not solely by active content, because high-viscosity mill bases can exhibit delayed foam collapse until the product reaches the holding tank.

    Compliance checklist for KS-7709 MXHF-Solution Silicone Defoamer by downstream segment
    Downstream segmentRegulatory or industry frameworkTest method / referenceControl parameter
    Waterborne architectural coatingsGB 18582-2020, FDA 21 CFR 176.200ASTM D3960-16VOC and food-contact component limits
    FermentationFDA 21 CFR 173.340, Regulation (EC) No 1333/200821 CFR 173.340Dimethylpolysiloxane residue limit
    Textile dyeingOEKO-TEX Standard 100, ZDHC MRSL v3.1REACH Annex XVIID4/D5/D6 below 0.1 wt%
    Pulp and paper wet endFDA 21 CFR 176.210, BfR Recommendation XXXVI21 CFR 176.210Defoamer residue in food-contact paper
    Industrial cleaningEU 648/2004ASTM D3601Foam height in aqueous media
    Agrochemical SCEPA 40 CFR 180.910, CIPAC MT 47.2CIPAC MT 47.2Persistent foam after 60 seconds
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    Certification & Compliance
    More Introduction

    KS-7709 MXHF-Solution Silicone Defoamer is a pumpable silicone-polyether foam-control agent supplied for use in aqueous industrial systems where surfactant-stabilized macrofoam and entrained air reduce throughput, pump efficiency, heat transfer, and film quality. The model designation KS-7709 identifies a specific silicone-polyether solution grade, while MXHF indicates a hybrid chemistry in which a methylsiloxane backbone carries pendant polyether groups to provide self-emulsification in water without the high water content of a conventional emulsion. The product is applied in waterborne coatings, printing inks, emulsion polymerization, metalworking fluids, agricultural suspensions, and pigment dispersions. It differs from mineral oil defoamers in its lower active-phase surface tension and from standard silicone emulsions in its lower water content and preservative demand. Published data for the exact KS-7709 MXHF-Solution configuration in peer-reviewed public literature is limited; supplier certificates of analysis and technical service reports remain the primary technical references. Any manufacturing specification should therefore be based on lot-specific release data rather than on class-typical numerical profiles alone.

    Composition, Appearance, and Release-Controlled Specification Ranges

    Because KS-7709 MXHF-Solution is a compounded silicone-polyether liquid rather than a chemically pure substance, its release profile is defined by viscosity, density, nonvolatile matter, pH, and foam knockdown response. For silicone-polyether solution defoamers in the same product class, low-shear viscosity measured by ASTM D2196 at 25 °C is typically 200–800 mPa·s. Density measured by ASTM D4052 at 25 °C is generally 0.98–1.02 g/cm³. Nonvolatile matter determined by ASTM D2369 after 2 h at 105 °C commonly falls between 10 wt% and 20 wt% for solvent-free silicone-polyether grades; if a given KS-7709 MXHF-Solution lot contains a volatile carrier, nonvolatile matter is handled as a separate release parameter. A 1 wt% dispersion pH measured by ASTM D1293 is typically 6.5–8.0. The silicone active phase generally exhibits a kinematic viscosity in the 500–5,000 cSt range, which controls spreading rate and drainage at the foam lamella. The product is nonionic to weakly anionic, reducing sensitivity to hard-water calcium ions and permitting incorporation into anionic or nonionic surfactant packages. Cationic additives and quaternary ammonium biocides require preliminary compatibility screening because charge attraction can disturb the dispersion and lower defoamer response. These class-typical values are not certificates of analysis for KS-7709; each production lot should be released only against the supplier’s approved specification limits.

    Comparative class profile for KS-7709 MXHF-Solution silicone defoamer versus conventional defoamer types
    ParameterKS-7709 MXHF-Solution classSilicone emulsionMineral oilPolyether glycol
    ChemistrySilicone-polyether hybrid solutionSilicone oil plus hydrophobic silicaMineral oil plus hydrophobic solidsEO/PO block copolymer
    Water dispersibilitySelf-emulsifying microdispersionWhite macroemulsionNot self-emulsifyingWater-soluble or dispersible
    Active-phase surface tension20–22 mN/m20–22 mN/m28–32 mN/m30–35 mN/m
    Typical use level0.05–0.5 wt%0.05–0.5 wt%0.2–1.0 wt%0.1–0.5 wt%
    Over-dose defect riskCratering and intercoat adhesion loss possibleLarge-droplet crawling and fisheye riskGloss loss and oil separationWater sensitivity and reduced water resistance

    What separates KS-7709 MXHF-Solution from mineral oil and polyether defoamers in high-surfactant media?

    In formulations containing large fractions of ethoxylated nonionic surfactants or high-HLB emulsifier packages, mineral oil defoamers frequently lose activity because the oil droplets are solubilized or stabilized by the surfactant monolayer, reducing the oil spreading coefficient and preventing film rupture. Silicone defoamers retain a low active-phase surface tension, typically 20–22 mN/m, which maintains a positive spreading coefficient at the foam lamella even when surfactant concentration exceeds the critical micelle concentration. KS-7709 MXHF-Solution carries polyether functionality that converts the silicone active into a self-emulsifying liquid; under mild agitation, it forms a fine microdispersion rather than floating as a discrete oil layer. This behavior is mechanistically different from a conventional silicone emulsion, which is supplied as a pre-formed aqueous macroemulsion with preservatives and may be prone to separation and microbial growth during storage. Compared with pure polyether defoamers, the methylsiloxane segment provides lower surface tension and less temperature-dependent solubility, which can be advantageous in coating lines where recirculating paint or ink temperatures rise above 40 °C. However, the same silicone activity can lower dynamic surface tension at the coating-air interface, and over-addition above 0.5 wt% may generate cratering, poor intercoat adhesion, and surface slip. The practical use window in aqueous acrylic and styrene-acrylic paint is usually 0.1–0.3 wt%; this range is formulation-specific and requires gradient testing.

    In a 1,000 L latex paint letdown tank equipped with a Cowles disperser operating at tip speed 5–8 m/s, KS-7709 MXHF-Solution is typically added after the grind stage. Addition during pigment dispersion can cause partial adsorption of the defoamer onto high-surface-area pigments, such as fumed silica and carbon black, reducing long-term deaeration performance. A split-addition method is used in high-foaming formulations: 50% of the total dose is introduced into the mill base to control air entrainment during grinding, and the remaining 50% is post-added during letdown to control macrofoam before filling. At total addition levels above 0.5 wt%, cratering and crawling may appear in waterborne alkyd and air-drying acrylic enamels; adhesion loss after intercoat application is evaluated using ASTM D3359 cross-hatch. Because the defoamer migrates to the coating-air interface, repeated oven aging and humidity exposure can alter its distribution; long-term recoatability should be tested under ISO 6270-1 condensation conditions when exterior durability is required.

    When Alkaline pH Drift and Calcium Hardness Load the Defoamer Interface

    In aqueous alkaline cleaners and metalworking fluids, pH drift above 9.5 and calcium ion concentrations above 200 mg/L can destabilize conventional silicone emulsions and increase coalescence of the silicone droplets. KS-7709 MXHF-Solution is designed to tolerate moderate alkalinity and hard water because its polyether segments provide steric stabilization that is less dependent on electrostatic repulsion. In semisynthetic metalworking fluid concentrates containing sulfonate emulsifiers, alkanolamine corrosion inhibitors, and 15–20 wt% naphthenic oil, the defoamer is introduced at 0.05–0.2 wt% of the concentrate before pH adjustment. High-pressure coolant delivery at 10–20 bar releases dissolved air and generates macrofoam in the working dilution; foam height measured by ASTM D892 in a 5 vol% dilution is used as a screening parameter. End-user validation is required because sump geometry, tramp oil contamination, and bacterial load change foam character. The defoamer is hydrolytically stable through pH 6–10, but prolonged exposure above pH 10.5 may degrade the polyether functionality and reduce self-emulsification; storage tanks should be vented and protected from prolonged exposure to strong caustic.

    During batch emulsion polymerization of vinyl acetate-ethylene and acrylic latices, unreacted monomer stripping creates stable foam that raises reactor pressure and lowers heat-transfer coefficient. KS-7709 MXHF-Solution is generally post-added at 0.05–0.2 wt% after residual monomer stripping, because silicone-polyether products with unsaturated groups may interfere with radical propagation if added during polymerization. Addition before polymerization should be avoided unless the supplier confirms that the grade is inert to the initiator system. The defoamer can be pre-diluted with demineralized water at a 1:1 ratio to improve metering accuracy at low use levels; static mixers or low-shear recirculation loops are preferred for in-line injection. In a 200 L pilot batch of semisynthetic coolant, pre-dilution before dosing reduced localized viscosity spikes during concentrate mixing and prevented gel formation in low-shear blending equipment.

    High-shear persistence and filter response are governed by droplet size, not active content

    Waterborne printing inks for flexographic and gravure presses generate stable microfoam in recirculation systems because the inks contain acrylic solution polymers, pigments, and high-speed pump shear. In a flexographic press with an anilox roll and doctor blade chamber, entrained air increases viscosity and produces print mottle. KS-7709 MXHF-Solution is added at 0.1–0.3 wt% of the finished ink; the self-emulsifying silicone-polyether structure preserves defoaming under the sustained high-shear of a press pumping loop. In a recirculation loop with a diaphragm pump and an in-line 50–100 μm bag filter, coarse defoamer droplets can collect on the filter and increase pressure drop. The polyether modification of KS-7709 MXHF-Solution is intended to generate droplet sizes below 50 μm under standard mixing; particle-size distribution measured by ISO 13320 laser diffraction should be checked after dilution when filter blockage is a concern. Compared with mineral oil defoamers, the silicone-polyether solution has lower water-phase solubility and is less likely to be stripped from the ink by evaporation; compared with silicone emulsions, its lower water content reduces the dilution of ink solids during addition.

    Compliance documentation checklist for KS-7709 MXHF-Solution silicone defoamer
    RequirementStandard or regulatory referenceApplication
    Hazard communicationOSHA 29 CFR 1910.1200Safety data sheet and label review
    European market registrationREACH Regulation (EC) No 1907/2006Manufacturer registration and SVHC disclosure
    Restriction of hazardous substancesEU RoHS Directive 2011/65/EUApplicable only to electrical and electronic equipment; not a general coating clearance
    Food-contact useFDA 21 CFR 176.170Not assumed; supplier clearance and migration data required
    Packaging and transportASTM D3951Commercial packaging compatibility

    Storage of KS-7709 MXHF-Solution should be in closed, vented containers at 5–40 °C. Freeze-thaw cycling may cause phase separation in silicone-polyether solutions; if the material freezes, it should be reconditioned under controlled agitation and tested before use. The product should not be combined with strong oxidizing agents, strong cationic polyelectrolytes, or amine catalysts without compatibility screening. In moisture-sensitive polyurethane systems, water introduced with any defoamer must be accounted for in the isocyanate index calculation. Published data for the KS-7709 MXHF-Solution in moisture-sensitive polyurethane and radiation-cured systems is limited; lab-scale compatibility testing is required before production use.