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XIAMETER ACP-0100 Hydrophobic Silica-Enhanced Silicone Antifoam

    • Product Name: XIAMETER ACP-0100 Hydrophobic Silica-Enhanced Silicone Antifoam
    • 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 559141
    Product Name XIAMETER ACP-0100 Hydrophobic Silica-Enhanced Silicone Antifoam
    Appearance White viscous liquid
    Active Content 100%
    Chemical Composition Polydimethylsiloxane with hydrophobic silica
    Viscosity At 25 C 5000 mPa·s
    Flash Point >100°C
    Freezing Point -50°C
    Water Solubility Insoluble
    Shelf Life 24 months

    As an accredited XIAMETER ACP-0100 Hydrophobic Silica-Enhanced Silicone Antifoam factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied as a 25 kg pail or 200 kg drum of XIAMETER ACP-0100 hydrophobic silica-enhanced silicone antifoam compound.
    Container Loading (20′ FCL) One 20′ FCL containing palletized drums of XIAMETER ACP-0100, secured and protected for safe transit.
    Shipping XIAMETER ACP-0100 ships as a non-regulated, non-hazardous industrial chemical. Available in drums or totes, it travels via standard ground freight. Keep containers sealed, dry, upright, and protected from freezing or excessive heat during transit. Unopened, it maintains shelf life for 24 months under recommended storage conditions.
    Storage Store XIAMETER ACP-0100 in its original, tightly sealed container in a cool, dry, well-ventilated area. Protect from direct sunlight, heat sources, and oxidizing agents. Recommended storage temperature is between 0°C and 32°C; avoid freezing. Keep containers closed when not in use to prevent contamination. Proper storage maintains product quality until expiry.
    Shelf Life Shelf life is 24 months from manufacture when stored in original, unopened containers at recommended temperatures.
    Application of XIAMETER ACP-0100 Hydrophobic Silica-Enhanced Silicone Antifoam

    In kraft pulp brownstock washing, weak black liquor at 70–85 °C and pH 12.0–13.5 carries saponified tall oil soaps, alkali lignin fragments, and residual sulfur compounds. Foaming in vacuum drum washer filtrate tanks and falling-film evaporator effect bodies lowers heat-transfer coefficients, raises differential pressure across demister pads, and forces liquor carryover into condensate return lines. Weak black liquor solids in this zone typically move from 15–25 wt% at the washer stage toward 65–80 wt% in strong black liquor storage, but foam is most severe in the intermediate washer filtrate range where tall oil soap surface activity peaks. XIAMETER ACP-0100 is hydrophobic and is not self-emulsifying in black liquor. Continuous dosing is therefore achieved by prediluting the compound to 1–5 wt% in a low-aromatic hydrocarbon or white mineral oil carrier and injecting it through a positive-displacement diaphragm metering pump into the weak liquor line upstream of the filtrate tank. A static mixer or an injection quill located at least 10 pipe diameters upstream of the vessel inlet disperses the compound without generating the high-shear droplet breakdown that can deactivate the hydrophobic silica network. Field screening in this service usually begins at 5–20 ppm active antifoam on a dry fibre basis and is titrated against foam collapse time measured by a heated sparge apparatus aligned with ASTM E2407. Evaporator demister differential pressure is monitored with a pressure transmitter on each effect; sustained differential pressure above 250 mm H2O typically indicates foam carryover and requires dose adjustment. Overdosing above the minimum effective level is avoided because excess hydrophobic silica can deposit on digester screens and increase extractives deposition on washer wire. Alkaline hydrolysis of the silica-silicone matrix becomes a processing risk at pH >12.5 and temperature >80 °C; continuous evaluation under mill-specific weak black liquor composition is therefore required before permanent dosing. The downstream products include bleached hardwood and softwood market pulp, linerboard, and sack paper. Where the finished paper or board is intended for aqueous or fatty food contact, the formulator must confirm extraction limits under FDA 21 CFR 176.170 and FDA 21 CFR 176.180.

    What Foam Collapse Thresholds Are Observed in Activated Sludge Aeration Basins?

    Because mixed liquor in municipal and industrial activated sludge basins contains hydrophobic actinobacteria, extracellular polymeric substances, and biodegradable surfactants, persistent foam can build to 0.3–1.0 m above the aeration tank surface and overflow into walkways or clarifier scum boxes. The foam is most severe in systems operating at high solids retention time of 10–20 days and mixed liquor suspended solids of 2,500–8,000 mg/L. ACP-0100 is prediluted to 0.5–2% in service water and injected continuously into the return activated sludge line or the aeration basin influent channel through a low-shear positive-displacement pump. Initial screening commonly begins at 1–10 ppm active antifoam on influent flow and is adjusted after observing foam persistence in the aeration basin and secondary clarifier. Laboratory evaluation under ASTM E2407 can use filtered mixed liquor or clarified effluent spiked with the plant surfactant load to compare collapse time and knockdown capacity. Overdosing above the minimum effective dose is a documented operational boundary: silicone films can lower the volumetric oxygen transfer coefficient of fine-bubble diffuser grids and mechanical surface aerators, so clean-water oxygen transfer efficiency must be re-checked after dose changes using a standard aeration test. In membrane bioreactors with mixed liquor suspended solids above 10,000 mg/L, the compound must be pilot-tested because residual silicone can interact with membrane surfaces and increase trans-membrane pressure in submerged flat-sheet or hollow-fibre modules. The final product is treated municipal or industrial effluent discharged under the plant’s NPDES permit; visible sheen and defoamer-related foaming in the receiving stream are treated as permit exceedances.

    Application zoneReference standard or methodOperational variable to verify
    Kraft mill paper and board food contactFDA 21 CFR 176.170, FDA 21 CFR 176.180Extraction limits for aqueous and fatty food simulants
    Defoamer efficacy in aqueous mediaASTM E2407Foam collapse time and knockdown persistency at process temperature
    Agrochemical inert ingredient status40 CFR 180.910Exact CAS registry composition under U.S. pesticide registration
    Accelerated storage of liquid agrochemical formulationsCIPAC MT 46.3Phase separation, viscosity drift, sedimentation at 54 °C for 14 days
    Textile absorbency after processingAATCC TM79Residual silicone deposition on dyed fabric

    High-Shear Jet Dyeing Machines Demand Rapid Deaeration at 110–135 °C

    In sealed horizontal jet dyeing machines, polyester and polyamide fabrics are processed at nozzle pressures of 1.5–3.0 bar, bath ratios of 1:5–1:8, and final dyeing temperatures of 130–135 °C for polyester and 110–120 °C for polyamide. The polyester bath pH is commonly controlled at 4.5–5.5 with acetic acid and sodium acetate; the polyamide bath pH is controlled at 6.0–7.0. Foam is generated as the dye bath passes through the jet venturi and returns to the storage chamber; entrained air becomes trapped in rope folds, causing crease marks, fabric floatation, and circulation pump pressure fluctuation. ACP-0100 is prediluted with cold water to a 0.5–2% stock and metered into the circulation return sump after the dye leveling agent has dissolved. Evaluation commonly begins at 0.05–0.2 g/L of bath volume and is reduced if dye specking or silicone spot deposition appears on dark shades. Because high shear in the jet nozzle can break the silicone-silica droplet, the addition point is placed in the lower-shear storage chamber or the return sump, not directly into the nozzle throat. The compound is normally added at 60–70 °C during the heating ramp. Addition above 120 °C without pre-dispersion in water can cause localized deposition on fabric surfaces. A fabric absorbency check under AATCC TM79 is used on the unloaded dyed fabric to detect residual silicone. Final products are dyed woven and knitted polyester for activewear, automotive textiles, and home furnishing. Published production-scale data for this specific compound on dark polyester shades is limited, so pre-production head-end trials are required before bulk dosing.

    Formulating a water-based suspension concentrate requires control of air entrainment during the surfactant wetting phase and during horizontal bead milling of active ingredients such as azoxystrobin, tebuconazole, or chlorothalonil. The rotor-stator pre-dispersion step and the high-speed disperser blade draw air into the viscous millbase. If the entrained air is not collapsed before letdown, apparent viscosity rises, mill outlet temperature fluctuates, and the filling line cannot maintain target density. ACP-0100 is introduced at the letdown stage after the bead mill has reduced the median particle size to 1–5 µm, normally at 0.05–0.2% by batch weight. Adding the hydrophobic compound before the bead mill can reduce grinding efficiency and produce undispersed silicone droplets in the final formulation. The letdown tank is agitated with a low-shear swept-wall anchor impeller at 20–60 rpm for 15–30 min after the addition. The millbase temperature is held at 20–30 °C during defoamer addition; above 35 °C, surfactant-generated foam becomes more difficult to mitigate. The compound is not self-emulsifying in water, so a small addition to the oil phase during the surfactant melt stage improves dispersion in the finished SC. Storage stability of the filled suspension concentrate is checked at 54 °C for 14 days according to CIPAC MT 46.3 or the company’s equivalent internal protocol. For crop protection products sold in the United States, the inert ingredient status of the exact CAS registry composition under 40 CFR 180.910 must be confirmed before manufacture for agricultural use. The final products are packaged fungicide, insecticide, and herbicide suspension concentrates for in-field tank mixing.

    When Monoethylene Glycol Regeneration Loops Accumulate Hydrocarbon-Stabilized Foam

    Rich monoethylene glycol leaving a gas dehydration contactor carries dissolved hydrocarbons, corrosion inhibitors, iron sulfide particles, and high concentrations of divalent salts. During regeneration, the rich glycol is depressurized from pipeline pressure into a flash separator operating at 5–20 bar and then heated in a vacuum reboiler where foam can destabilize level control, reduce heat-transfer rate, and force glycol into the reflux drum and produced-water discharge. ACP-0100 is injected continuously into the rich MEG line upstream of the flash drum after predilution in lean MEG or a low-aromatic hydrocarbon carrier. Initial screening in this service commonly starts at 10–50 ppm active antifoam on rich MEG flow and is adjusted with a pressurized nitrogen-sparged foam column aligned with ASTM E2407. The reboiler operates at 120–140 °C and pH 8–10; the compound must withstand this thermodynamic window without forming hard deposits on reboiler tubes or structured packing. Overdosing can result in silicone plating on heat-transfer surfaces, especially in the presence of high divalent salt load. Amine-based corrosion inhibitors and quaternary ammonium filmers may alter droplet size and antifoam performance, so pilot testing must be conducted with the actual rich MEG composition rather than with a synthetic substitute. Published production-scale data for this specific configuration in highly sour gas plants is limited; the compound must be qualified by a side-stream trial before full-flow injection. The final product is lean monoethylene glycol reused for hydrate inhibition in gas production.

    Clean-in-place detergent recirculation in dairy, brewery, and beverage plants requires a collapsed headspace so that spray balls and rotating jet heads deliver full impingement pressure to tank walls. ACP-0100 is introduced into the CIP return line at 10–50 ppm of recirculated detergent volume only after foam generation has been confirmed by sight-glass level rise; excessive use in a closed CIP circuit can leave silicone residue on spray equipment. The compound is not for direct food-contact use in this configuration; final rinse verification under ATP or conductivity protocols is used to confirm detergent removal.

    Fermenter Headspace Foam Control Under Sterile Feed Conditions

    During fed-batch aerobic fermentation of Escherichia coli, Pichia pastoris, or Saccharomyces cerevisiae, headspace foam is stabilized by extracellular proteins, polysaccharides, and cell lysis debris under airflow rates of 0.5–2.0 vvm, agitation at 200–800 rpm, and backpressure of 0.3–1.0 bar. The foam can push through the exhaust condenser, block the sterile gas filter, and cause liquid carryover into the vent line. ACP-0100 is metered through a sterilizable positive-displacement pump into the bioreactor headspace or into the feed line after the sterile filter. The compound is hydrophobic and must be autoclaved in a sealed vessel at 121 °C for 30 min before use in sterile processes. Initial trials are commonly conducted at 0.01–0.1% v/v on working volume, and the minimum effective dose is determined by a foam-height rise test under process aeration and agitation. Overdosing reduces the volumetric oxygen mass transfer coefficient kLa because silicone film spreads at the air-liquid interface and retards oxygen diffusion. Off-gas analysis or a dynamic gassing-out test in the production vessel is used to quantify the impact. The antifoam is generally added after inoculation and before feeding begins; during the initial lag phase, cell surface hydrophobicity is low and the requirement can be overestimated. In downstream processing, residual silicone can foul tangential-flow filtration membranes, so the harvest is clarified with a depth filter or centrifuge before column capture. The final products are recombinant enzymes, bioethanol, organic acids, and monoclonal antibody fragments.

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    Certification & Compliance
    More Introduction

    XIAMETER® ACP-0100 Hydrophobic Silica-Enhanced Silicone Antifoam is a 100 % active silicone antifoam compound supplied as an opaque, off-white viscous liquid. The product combines a linear polydimethylsiloxane fluid with treated hydrophobic silica particles dispersed in the silicone phase. Because the continuous phase is anhydrous and free of external emulsifiers, the material introduces no water, biocides, or surfactants into the process stream. This removes freeze-thaw instability, preservative demand, and separation tendency associated with water-diluted silicone antifoam emulsions. The primary function is foam destabilization through a surface-spreading and particle-bridging mechanism that disrupts the adsorbed surfactant layer and reduces lamella elasticity.

    Compositionally, the product belongs to the class of silica-filled silicone compounds in which hydrophobized fumed silica provides the solid surface required for bubble-film rupture and the siloxane fluid provides the mobile oil front. The exact silica loading and siloxane molecular weight are not disclosed in public technical bulletins. The material exhibits non-Newtonian, shear-thinning rheology typical of silica-thickened silicone compounds; apparent viscosity decreases with increasing shear rate, and the silica network may rebuild after low-shear rest. Lot-release documentation may include Brookfield rotational viscosity at 25 °C and density at 25 °C, but the certificate of analysis should be used for incoming inspection because exact batch values are not fixed constants.

    The product is insoluble in water and lower alcohols but is dispersible in aliphatic and aromatic hydrocarbons and in some ketones under low-shear agitation. This solubility profile determines equipment-cleaning practice and should be reviewed before solvent flushing. Because the product is water-free, concentrate storage does not support bacterial growth; however, residual silicone droplets in dilute aqueous process streams can associate with suspended solids or biofilm if overdosed.

    Table 1 summarizes the analytical and regulatory reference framework used for release and safety documentation. Product-specific numerical limits are taken from the current certificate of analysis or safety data sheet.

    Parameter or obligationReference method or standardPurpose
    Kinematic viscosity of opaque liquidASTM D445 / ISO 3104Lot release, rheological consistency
    Density at 25 °CASTM D1298 / ISO 12185Incoming inspection
    Flash pointASTM D92 / ISO 2592Safety classification and storage
    VOC content, if requiredUS EPA Method 24Regulatory reporting
    EU REACH registrationEC 1907/2006 Annex IISafety data sheet and registration
    EU CLP classificationRegulation (EC) No 1272/2008Hazard communication

    How Does Hydrophobic Silica in Silicone Fluid Destabilize a Foam Lamella?

    The defoaming action is controlled by two interacting mechanisms. The silicone phase has a surface tension below 22 mN/m at 25 °C, lower than the equilibrium surface tension of most aqueous surfactant solutions, so a droplet placed on a foam film spreads as a positive spreading coefficient develops. The spreading oil raises the local surface pressure and displaces surfactant molecules, reducing film self-healing. The hydrophobic silica particles then function as solid bridges; the aqueous film dewets from the treated particle surface when the three-phase contact angle exceeds 90°, puncturing the lamella. This bridging-dewetting process is faster than rupture by a pure silicone oil because the particle lowers the energy barrier for hole nucleation.

    On production-scale equipment, the addition point governs retention of particle-bridging activity. Injection downstream of a rotor-stator homogenizer with tip speeds above 20 m/s can over-disperse the compound or strip hydrophobized silica from the silicone–water interface, reducing knockdown speed. In recirculation loops, the product is instead introduced after the pump impeller but before a low-shear static mixer so that the silicone is dispersed as droplets large enough to reach the foam interface. A modified sparging test with a calibrated gas flow of 1.0 L/min in a 2 L column can be used to compare knockdown time and residual foam height; no single ASTM or ISO method covers all aqueous and non-aqueous process foams, so plant-specific validation is typically necessary.

    Over-addition is a critical threshold risk in systems with high surfactant loading or high interfacial area. In low-foaming aqueous streams, a dose of 5 mg/kg is often adequate. When surfactant concentration exceeds the critical micelle concentration by an order of magnitude, the surfactant micelles can solubilize or emulsify silicone droplets, producing a non-linear dose response: foam height may remain unchanged until saturation, after which residual silicone appears as surface oil, filter matting, or membrane fouling. The lowest effective addition level should therefore be determined in the actual process fluid. Published data for this specific product in membrane bioreactors is limited; the operational boundary is inferred from the general behavior of 100 % active silicone compounds.

    Comparative Positioning Against Emulsion, Polyether, and Mineral Oil Defoamers

    Compared with mineral oil defoamers, the silicone compound contributes no mineral oil fraction and generally requires lower active dosage in high-temperature or high-surface-energy systems. Mineral oil defoamers are often applied at 0.05–1.0 % by volume, whereas silicone compounds may be effective in the range of 1–50 mg/kg in many industrial foaming systems. Mineral oil remains preferred when cost per kilogram is the dominant criterion or when silicone contamination of painted or coated surfaces cannot be tolerated. Polyether defoamers exhibit inverse solubility at the cloud point and can provide clarity in water-based clearcoats; however, their antifoam efficiency may decline above the cloud point or in high-electrolyte brines. Conventional silicone emulsions offer convenient dilution but contain water and surfactants, require freeze protection, and may need preservatives in storage.

    Defoamer classContinuous phaseTypical active contentPrimary advantagePrimary limitation
    Hydrophobic silica-enhanced silicone compoundAnhydrous silicone100 %High knockdown at low dose, no water loadRequires shear dispersion; residual silicone may foul
    Silicone emulsionWater10–30 %Easily diluted at point of useFreeze-thaw instability, preservative demand
    Mineral oil defoamerMineral oil5–30 %Low costHydrocarbon carryover, higher dosage
    Polyether defoamerWater or solvent10–40 %Clarity and compatibility in some coatsCloud-point dependence, limited high-temperature efficiency

    Storage in closed containers at 5–40 °C is recommended to minimize water ingress and maintain particle distribution. The product is incompatible with strong oxidizing agents and should not be heated above the flash point reported in the safety data sheet. Transfer lines and storage tanks constructed of stainless steel, carbon steel, glass, or polypropylene are generally suitable; ethylenepropylene diene monomer and natural rubber seals may swell after prolonged exposure, so polytetrafluoroethylene or perfluoroelastomer is preferred for gaskets. The expected shelf life is 24 months from the date of manufacture when kept in unopened containers; current technical bulletins should be used to confirm batch-specific stability.

    For high-shear dispersion applications, the product can be pre-emulsified into a suitable nonionic surfactant package at the point of use, but the resulting emulsion is not stable for long-term storage and must be used within the shift. High-pressure homogenizers with two-stage valves can produce droplet sizes below 5 µm; such droplets may be less effective at bridging large foam bubbles and may remain in the bulk. The compound should not be mixed with concentrated acids or bases without trial because siloxane condensation can be catalyzed, leading to viscosity increase. In solvent systems containing significant water, hydrolysis is negligible at normal pH 3–9 and ambient temperature.

    When Water-Free Delivery Is Required in Non-Aqueous Chemical Processing

    In non-aqueous applications such as solvent recovery, amine scrubbing, or crude oil separation, the anhydrous continuous phase of the product prevents water carryover into distillation columns and avoids the introduction of water-in-oil emulsion precursors. However, the product must be dispersed by process turbulence; a static mixer with 8–12 elements or a circulation loop with a Reynolds number above 10,000 in the injection zone is typically used. If the process fluid viscosity exceeds 500 mPa·s, pre-dilution in a compatible low-viscosity silicone fluid or a suitable process solvent may be necessary. Published data for this specific configuration is limited; the dispersion requirements are derived from the known rheology of 100 % active silicone compounds.

    For aqueous systems with high protein or starch foam loads, the product should be introduced at a point of maximum turbulence and as far upstream as practical to allow silica particles to encounter the foam interface before being encapsulated by surface-active constituents. Because the product is water-free, it does not provide a self-emulsifying response; if injection is stopped, foam control ceases once the dispersed silicone droplets are carried out of the process stream. Re-dispersal after the initial dilution should be avoided because repeated shear cycles can reduce activity. The operational boundary is therefore defined by shear history, surfactant concentration, and the compatibility of residual silicone with downstream separations, rather than by a single fixed addition rate.