| HS Code | 664943 |
| Appearance | milky white liquid |
| Active Content | 100% |
| Viscosity | low viscosity |
| Ph | 6.0-8.0 |
| Specific Gravity | 0.85-0.95 |
| Solubility | water-dispersible |
| Fda Compliance | complies with FDA 21 CFR 176.170 and 176.180 |
| Defoaming Effectiveness | rapid and persistent foam suppression |
| Recommended Dosage | 0.1%-0.5% based on total formulation |
| Shelf Life | 12 months when stored at room temperature |
As an accredited DF-588 FDA-Grade Waterborne Mineral Oil Defoamer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in 55-gallon (208 L) drums or 5-gallon pails with secure, resealable lids for safe storage and dispensing. |
| Container Loading (20′ FCL) | 20′ FCL shipment of DF-588 FDA-grade waterborne mineral oil defoamer, packed in sealed drums, palletized, secured, and labeled for safe transport. |
| Shipping | DF-588 ships in sealed, tamper-resistant containers (pails or drums) to prevent leakage and contamination. Classified as non-hazardous, it is transportable by ground, sea, or air without dangerous-goods restrictions. Ensure containers are upright, protected from freezing/extreme heat, and labeled for FDA-grade food-contact use. |
| Storage | Store DF-588 in its original, tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight and incompatible materials. Avoid extreme heat or freezing; recommended storage temperature is 5–40°C. Keep containers upright to prevent leakage, and use within shelf life to maintain product performance. |
| Shelf Life | DF-588 has a shelf life of 12 months when stored in sealed containers at moderate temperatures away from direct sunlight. |
In single-pass blade coating of food-grade board for aqueous and fatty food packaging, foam entrained during clay and calcium carbonate dispersion remains a measurable process variable when coater speeds exceed 1,200 m/min. DF-588 FDA-grade waterborne mineral oil defoamer is introduced into the dispersion phase before latex binder addition, normally at 0.05 to 0.3 wt% based on wet coating mass. The addition point is the coating kitchen slurry tank after titanium dioxide and clay have been wetted under a Cowles disperser operating at tip speeds from 18 to 25 m/s. Adding the defoamer after the latex binder produces micro-pinholes in the consolidated coating because oil droplets compete with binder adsorption on pigment surfaces; pinhole density is assessed under 40× stereomicroscopy after forced-air drying at 150 °C for 2 seconds. Rotational viscosity is measured at 100 rpm according to ISO 2555 with a Brookfield RVT spindle 3, and the air release property is considered sufficient when the pan viscosity remains within ±15 percent of the reference air-free formulation. The mineral oil phase remains within the 21 CFR 176.170 component listing when the cured board is tested with aqueous and fatty food simulants under 21 CFR 176.170(b) conditions. For cup stock and frozen food cartons, the limiting variable is not foam knockdown but retained coating smoothness; surface roughness Ra should remain below 1.5 μm as measured according to ISO 4287 after calender loading at 80 kN/m. Foam collapse in the recirculating coating pan is monitored by comparing air content in the delivery line against a pycnometric density measurement before the blade. Terminal food-contact articles include paper drinking cups, frozen food folding cartons, and quick-service sandwich wraps where the coated layer is separated from food by a functional barrier or by board structure meeting 21 CFR 176.170(c) for fatty food restrictions.
On chamber doctor blade systems printing water-based flexographic and gravure inks for indirect food packaging, foam becomes process-limiting at press speeds above 250 m/min. DF-588 is dosed into the letdown tank rather than the bead mill. The high shear of a bead mill at 1,500 to 2,000 rpm can over-disperse a mineral oil defoamer and reduce long-term knockdown performance. The addition range is 0.1 to 0.5 wt% based on finished ink mass. Ink viscosity is controlled by a DIN 6 mm flow cup according to ISO 2431, with typical flow times of 18 to 25 seconds for flexographic inks at 25 °C. Foam generation is assessed by a modified ASTM D892 procedure in which air is passed through a 100 mL sample at 24 °C and 94 mL/min for 5 minutes; foam collapse time below 30 seconds is considered acceptable for high-speed stack presses. The defoamer must not rupture the thin ink film on the anilox roll or create fish-eye defects in solid prints; print mottle is inspected on corona-treated polyethylene film at 40× magnification after a drawdown with a 6 μm wedge bar. Compliance for the printed package lies with 21 CFR 175.300 when the ink is separated from food by a functional coating, or with the end-use article provisions of 21 CFR 176.170 if the ink is on the non-food-contact side of paperboard. Under EU food-contact rules, the printed packaging must comply with Regulation (EC) No 1935/2004 and, for plastic layers, EU 10/2011 migration testing using food simulants A, B, and D2. Terminal prints include indirect labels, paper wraps, and foil-laminated pouches where the ink is behind a barrier layer.
| Downstream track | Addition point | Typical dosage | Critical metric | Equipment basis |
|---|---|---|---|---|
| Food-grade board blade coating | Slurry dispersion before latex binder | 0.05–0.3 wt% wet coating | Viscosity deviation ±15% per ISO 2555 | Cowles disperser, air-knife blade coater |
| Water-based indirect ink | Letdown after bead mill | 0.1–0.5 wt% finished ink | ISO 2431 flow time 18–25 s | Chamber doctor blade press |
| Food-contact emulsion polymer | Post-stripping letdown | 0.05–0.2 wt% emulsion | Absolute pressure 20–30 kPa | Stirred vacuum stripping vessel |
| Cut produce flume water | Pump suction after hydrocyclone | 10–100 ppm recirculated water | Foam channel height ≤5 cm | Centrifugal recirculation pump, rotary drum washer |
| Fruit/beverage DAF effluent | Equalization tank ahead of flash mix | 2–20 ppm effluent | Foam blanket height ≤10 cm | Dissolved air flotation unit |
| Starch adhesive for paper sacks | Cooked adhesive holding tank | 0.05–0.2 wt% dry starch | Foam volume ≤50 mL | Steam jacketed scraper glue cooker |
Residual vinyl acetate and acrylic monomer stripping in food-contact emulsion polymer production creates persistent foam in the vacuum receiver and condensate line. DF-588 is introduced after polymerization inhibitor addition and before the residual monomer stripping step, at 0.05 to 0.2 wt% of finished emulsion. The stripping vessel operates at 60 to 70 °C and 20 to 30 kPa absolute pressure; foam carryover into the condenser raises headspace pressure and reduces heat transfer efficiency on the shell-and-tube condenser. The defoamer must remain effective after the emulsion is neutralized with ammonia or sodium hydroxide to a pH of 4.5 to 6.5, a condition that can destabilize silicone-based alternatives but is compatible with mineral oil formulations. Rotational viscosity is measured at 20 rpm and 25 °C according to ISO 2555 with a Brookfield RVT spindle 4; final viscosity below 1,500 mPa·s indicates that air release has occurred before drum filling. Coagulum is screened through a 100 μm bag filter. The emulsion is intended for laminating adhesives that comply with 21 CFR 175.105 for adhesives and 21 CFR 175.300 for resinous coatings when applied to food-contact laminates under dry and fatty food conditions. Terminal products include retortable pouch laminates and snack packaging where the adhesive is behind a functional barrier. Published data for this specific configuration is limited; the dosage range reflects waterborne mineral oil defoamer class performance in emulsion plants rather than a single commercial trial.
Hydrocooler and flume recirculation systems in cut produce plants develop foam when potato starch, leached pectin, and saponins from peas or beans accumulate in wash water. DF-588 is metered into the suction side of the flume water recirculation pump at 10 to 100 ppm based on measured air content and water flow rate. The addition point is after the hydrocyclone solids separator because the high centrifugal shear in the hydrocyclone can reduce antifoam droplet size to the point of emulsification. Flume water velocity is typically maintained at 0.5 to 1.5 m/s in open channels; foam height above the channel is a simple proxy for defoamer requirement and should not exceed 5 cm under maximum vegetable throughput. The defoamer is selected to meet 21 CFR 173.340 when used as a defoaming agent in the processing of food, with residual levels controlled by good manufacturing practice and final potable water rinsing. Surface water temperature after hydrocooling is often 2 to 5 °C, and mineral oil defoamers require turbulent mixing to spread on the air-water interface at low temperature. Centrifugal recirculation pumps with 1.5 to 3 kW motors provide sufficient mixing at dosing points downstream of the pump volute. Terminal products include frozen cut potatoes, peas, and carrot slices intended for retail and foodservice packs. Foam carryover into the rotary drum washer is the main failure mode if the defoamer is added too far upstream; the defoamer must be re-dosed at the washer inlet to prevent foaming inside the drum and on the belt discharge.
Surfactant-laden effluent from cleaning-in-place systems enters a fruit juice or brewery dissolved air flotation unit and generates a stable foam layer on the clarified water surface. DF-588 is dosed at 2 to 20 ppm into the equalization tank ahead of the flash mixer to collapse surface foam and prevent DAF sludge float from being re-entrained by rising air bubbles. The DAF unit operates with a recycle ratio of 20 to 35 percent and air saturation pressure of 400 to 600 kPa. Foam blanket height in the aeration basin is monitored by ultrasonic level sensors; a blanket above 10 cm at the beach scraper indicates under-dosing or anionic surfactant breakthrough. The mineral oil defoamer does not function as a primary coagulant; it must be dosed after pH adjustment to 6.8 to 7.8 with ferric chloride or polyaluminum chloride to avoid emulsion carryover in the clarified effluent. The clarified water is discharged to municipal sewer or recycled for non-food-contact floor scrubbing. Compliance is governed by the facility discharge permit and ISO 14001 environmental management requirements; the FDA-grade designation is relevant only where effluent spray or mist may contact processing areas. Terminal outcomes are lower foam-related carryover of suspended solids and a stable sludge blanket in the DAF unit. Published field data for DF-588 in this specific effluent matrix is limited, and jar testing with the actual effluent is required to set the 2 to 20 ppm window.
In corrugated board and paper sack gluing lines, alkaline starch adhesives foam when cooked starch is pumped through high-speed transfer lines and recirculated in the glue pan. DF-588 is added to the cooked adhesive at 55 to 60 °C, after the starch gelatinization peak but before the adhesive reaches the holding tank. The addition level is 0.05 to 0.2 wt% based on dry starch mass. If the additive is introduced before gelatinization, it can become trapped in the starch granule and reduce tack; if added below 50 °C, mineral oil droplets have insufficient mobility to spread across the air-liquid interface. The adhesive is steam-cooked in a jacketed glue cooker with an internal scraper agitator at 30 to 60 rpm, and the foam volume is measured in a graduated foam column after 100 mL of adhesive is shaken for 30 seconds at room temperature. Acceptable foam volume is below 50 mL, determined by visual meniscus. Viscosity is measured with a Bostwick consistometer; a flow distance of 3 to 8 cm in 30 seconds at 25 °C indicates that the defoamer has not thickened the adhesive. Compliance for paper sacks and corrugated food packaging is governed by 21 CFR 176.170 for components of paper and paperboard in contact with aqueous and fatty foods, and 21 CFR 176.180 for components of paper and paperboard in contact with dry food. Terminal articles include multi-wall paper sacks for flour and sugar, corrugated retail boxes, and board laminates where the starch adhesive is a component of the food-contact paper structure under 21 CFR 176.170(a) conditions. Failure to control foam in the glue pan causes skip-line bond lines on corrugator belts and reduced edge crush strength in combined board.
| Application | Primary standard | Secondary standard | Operational boundary |
|---|---|---|---|
| Food-grade board coating | 21 CFR 176.170(b) | EU 1935/2004 | Functional barrier required for fatty food contact |
| Water-based indirect ink | 21 CFR 175.300 | EU 10/2011 | Ink must be behind barrier layer or non-contact side |
| Food-contact emulsion adhesive | 21 CFR 175.105 | 21 CFR 175.300 | Post-stripping pH 4.5–6.5 |
| Cut produce flume water | 21 CFR 173.340 | GMP | Potable water rinse after processing |
| Beverage DAF effluent | ISO 14001 | Facility discharge permit | Incidental food-area contact only |
| Starch adhesive | 21 CFR 176.170 | 21 CFR 176.180 | Addition window 55–60 °C |
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DF-588 FDA-Grade Waterborne Mineral Oil Defoamer is supplied as a nonionic aqueous emulsion of hydrotreated white mineral oil, hydrophobic fumed silica, and food-contact-selected nonionic emulsifiers. The product is intended for foam control in aqueous polymer dispersions, paper and paperboard coating colors, starch-based size press formulations, and water-reducible flexographic or gravure inks where a non-silicone defoamer is required for subsequent overprinting, lamination, or film adhesion. The FDA-grade designation refers to component selection against the compositional requirements of 21 CFR 176.200 and 21 CFR 176.210, which govern defoaming agents used in paper and paperboard coatings and in the manufacture of paper and paperboard intended for food contact, along with relevant portions of 21 CFR 178.3570 for incidental-contact lubricant constraints. DF-588 is not a direct food additive; clearance applies to finished articles fabricated under the cited sections and subject to the extractive limitations of 21 CFR 176.170 or 21 CFR 176.180, depending on food type and end-use temperature.
The defoaming mechanism is based on oil-droplet bridging and hydrophobic-silica lamellae rupture. The emulsion droplet spreads across the aqueous film interface, displaces surfactant-stabilized foam films, and allows the hydrophobic silica particles to pierce the lamella. Because the continuous phase is water, the product can be metered directly into aqueous coating or ink letdown tanks without solvent dilution. The base mineral oil is selected for low odor, low unsaturation, and broad food-contact acceptance. Typical base-oil kinematic viscosity is controlled to 15–30 mm²/s at 40 °C when tested according to ASTM D445-21; this balances spreading rate against persistence in recirculating systems. The product contains no added formaldehyde, no alkylphenol ethoxylates, and no organohalogen solvents.
Manufacturer release testing covers non-volatile content, pH, low-shear viscosity, density, and emulsion stability. The release window is given in Table 1. Non-volatile content is determined by ISO 3251 at 105 °C for 3 h, a method selected because the mineral oil fraction is nonvolatile under these conditions. pH is measured on the as-supplied emulsion without dilution according to ASTM E70-19. Viscosity is read with a Brookfield RVT viscometer under ASTM D2196-20 at 25 °C using spindle 2 at 30 rpm; this is a low-shear specification that governs pumping and metering rather than end-use defoaming. Density is determined by ASTM D1475-13 at 25 °C. Emulsion stability is judged after 24 h in a 100 mL glass cylinder at 25 °C; visible creaming greater than 2 mm of clear top layer is a rejection criterion. Particle-size distribution is measured by laser diffraction according to ISO 13320:2020, with volume-median diameter controlled to 6–15 µm.
| Property | Test method | Release range or description |
|---|---|---|
| Appearance | Visual, 25 °C | Opaque white free-flowing emulsion |
| Non-volatile content | ISO 3251, 105 °C, 3 h | 28–32 wt% |
| pH | ASTM E70-19 | 6.5–8.5 |
| Brookfield viscosity | ASTM D2196-20, spindle 2, 30 rpm | 400–1200 mPa·s |
| Density | ASTM D1475-13, 25 °C | 0.98–1.02 g/cm³ |
| Ionic character | Electrophoretic mobility | Nonionic |
| Emulsion stability | 24 h, 100 mL glass cylinder | No sedimentation, no oil separation, creaming <2 mm |
The emulsion is intentionally nonionic. It must not be mixed directly with high-charge-density cationic wet-strength resins, polyamidoamine-epichlorohydrin solutions, or cationic retention aids above 0.5 wt% solution concentration without a jar test because charge neutralization can destabilize the oil/water interface and produce visible agglomerates. Droplets below 6 µm reduce knockdown efficiency because they are less able to bridge and rupture foam lamellae; droplets above 15 µm increase creaming and reduce storage stability. Lot-to-lot non-volatile content is controlled within ±1 wt% of the 30 wt% nominal value, which limits batch variance in coating pumps that are calibrated for a fixed additive flow rate.
Surface tension depression is mild compared with silicone chemistries. In a 0.1 wt% addition to a standard styrene-acrylic paper coating color, surface tension change measured by ASTM D1331-14 is typically less than 2–4 mN/m, whereas some silicone emulsions at equal addition lower the air/liquid surface tension to 22–24 mN/m. This limited surface tension depression is the physical basis for reduced cratering tendency relative to silicone defoamers in roll-applied coatings.
In curtain coating and high-speed blade coating, foam recycled into the wet film produces pinholes, ribbing, and coat-weight nonuniformity. On a blade coater running at 1,200 m/min with coating color solids of 60–64 wt% and Brookfield viscosity of 800–1,500 mPa·s, DF-588 is introduced into the letdown tank after starch cooking and pigment dispersion. The initial charge is 0.1–0.3 wt% on wet coating weight. Higher addition, up to 0.5 wt%, is used only after drawdown or sheet-defect assessment shows incomplete knockdown. Above 0.5 wt%, the mineral oil can deposit on drying surfaces, reduce gloss in clay-coated board, and produce visible oil exudation on the return side of the coating loop.
Addition must not be made before a high-shear disperser. Exposure to a Cowles blade at 10–20 m/s tip speed can split emulsion droplets below 1 µm and desorb the nonionic emulsifier. The resulting fines do not bridge foam films effectively and can create stable microfoam that passes through low-pressure filters and re-enters the application head. Plant metering is therefore performed with a progressive cavity or diaphragm pump; centrifugal pumps with impeller tip speed above 8 m/s are avoided. Dilution water should have pH between 5.0 and 8.5 and temperature below 35 °C. If plant water contains more than 500 ppm calcium carbonate hardness, predilution should be made with softened water or the product should be added without dilution to avoid forming calcium soaps with the nonionic emulsifier.
Water-reducible flexographic inks present a different foam problem. High-speed pump circulation and plate-cylinder return into the recirculation reservoir can entrain air, changing transfer density and dot gain. DF-588 is added to finished ink at 0.2–0.5 wt% of total ink mass, after pigment dispersion, because ink grinding with media mills above 3,000 rpm can destroy the emulsion. The defoamer is metered into the letdown tank and mixed under a low-tip-speed folding agitator until the ink appears streak-free. In plate-cylinder printing at 300–500 m/min, foam collapse should occur within 10–20 s after ink returns to the recirculation reservoir. If the ink contains more than 10 wt% ethanol or isopropyl alcohol, the emulsion may solubilize sufficiently to lose defoaming activity; in such cases, a mineral oil/silica paste rather than a waterborne emulsion is preferred. DF-588 is not recommended for solvent-based inks because water is the continuous phase and phase inversion will occur.
The differentiating performance characteristic of DF-588 is its non-silicone mineral oil chemistry. In waterborne coatings, silicone defoamers spread rapidly across the air/liquid interface and can produce craters and fish eyes if droplets reach the wet film surface at the wrong time. DF-588 does not generate the same surface tension gradient because the mineral oil surface tension is closer to that of the aqueous coating; therefore cratering is less likely, at the cost of lower ultimate knockdown under very high surfactant loads. In recirculating coating systems, mineral oil droplets are consumed more slowly than polyether defoamers because they are not fully soluble in the water phase. This gives longer persistence against tray foam but creates a heavier surface oil burden if overdosed.
| Parameter | DF-588 mineral oil emulsion | Silicone emulsion | Polyether polyol |
|---|---|---|---|
| Primary defoaming mechanism | Oil droplet bridging and hydrophobic-silica lamellae rupture | Rapid spreading on aqueous/air interfaces with large surface tension depression | Cloud-point deactivation and displacement of surfactant from interface |
| Typical use level | 0.1–0.5 wt% | 0.01–0.2 wt% | 0.2–1.0 wt% |
| Cratering risk | Low to moderate; formulation dependent | High if poorly dispersed | Low |
| Recoatability | Good after normal drying | Possible surface contamination retention | Good |
| FDA paper-coating clearance | Formulated for 21 CFR 176.200 and 21 CFR 176.210 | Many grades not listed | Grade dependent |
| Effect above top dose | Gloss reduction, oil exudation on dryer cans | Cratering, intercoat adhesion loss | Soft foam, clear film haze |
DF-588 should not be combined with strong oxidizing agents, concentrated mineral acids, or concentrated cationic coagulants. The emulsion is stable in the dark at 5–35 °C for 12 months; storage above 40 °C accelerates creaming. If freezing occurs, thaw at 20–25 °C and agitate with a folding paddle for 15 min. Do not use a high-shear mixer for thaw recovery. For food-contact paperboard, the finished article must be tested under the intended conditions of use according to the extraction cell protocols of 21 CFR 176.170 or the dry-food protocols of 21 CFR 176.180, because mineral oil migration into fatty foods is dosage-dependent. Published data for DF-588 in strongly acidic packaging media such as citrus-oil emulsions is limited; end-use extraction testing is required before commercial use. The product is classified as non-dangerous under Regulation (EC) No 1272/2008 [CLP], but oil mist formation should be avoided when the product is inadvertently oversprayed onto heated dryer surfaces.