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UCON RO-60 Polyalkylene Glycol Synthetic Oil Defoamer

    • Product Name: UCON RO-60 Polyalkylene Glycol Synthetic Oil 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 444693
    Appearance Clear, viscous liquid
    Odor Mild, characteristic synthetic oil odor
    Specific Gravity 20 20 C 1.00
    Kinematic Viscosity 40 C 60 cSt
    Kinematic Viscosity 100 C 12 cSt
    Viscosity Index 180
    Flash Point Coc 240°C
    Pour Point -35°C
    Refractive Index 25 C 1.450
    Solubility In Water Dispersible / soluble in water depending on system conditions

    As an accredited UCON RO-60 Polyalkylene Glycol Synthetic Oil Defoamer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing UCON RO-60 polyalkylene glycol synthetic oil defoamer is packaged in 55-gallon steel drums or 5-gallon pails, with net quantity per container.
    Container Loading (20′ FCL) 20′ FCL container loaded with UCON RO-60 Polyalkylene Glycol Synthetic Oil Defoamer, safely secured, documented, and ready for export shipment.
    Shipping UCON RO-60 polyalkylene glycol synthetic oil defoamer ships in pails, drums, or bulk totes. Transport is not regulated as hazardous per typical inland requirements. Keep containers sealed, protected from moisture, and upright. Standard freight handling applies; avoid extreme heat or freezing to preserve product integrity.
    Storage Store UCON RO-60 in its original, tightly closed container in a cool, dry, well-ventilated area away from direct sunlight, heat, and open flames. Protect from moisture and freezing, and keep separated from strong oxidizers and incompatible chemicals. Ensure containers are clearly labeled, secure against leaks, and stored within recommended temperature limits.
    Shelf Life Shelf life for UCON RO-60 is typically 2 years from manufacture when stored unopened in original, sealed containers away from heat and moisture.
    Application of UCON RO-60 Polyalkylene Glycol Synthetic Oil Defoamer

    When tramp oil ingestion in a central coolant system raises dilute emulsion foam height above the ASTM D3601 visual collapse criterion

    In central coolant reservoirs above 2,000 L, the polyalkylene glycol defoamer UCON RO-60 is introduced into the oil phase of the metalworking fluid concentrate before emulsification at 0.05–0.3 wt% of the concentrate, equivalent to 50–500 ppm in the final 5–8% sump emulsion. The addition is made under low-shear stirring at 40–50°C in a jacketed blend tank, not into the cold sump, because unemulsified droplets can separate in hard water above 250 ppm CaCO₃ hardness and deposit on high-speed spindle bearings. Compliance for foaming behaviour is assessed by ASTM D892 for the oil concentrate and ASTM D3601 for aqueous dilutions, with typical acceptance limits of ≤50 mL foam volume after 5 min of aeration and complete collapse within 10 min. Downstream production involving high-pressure through-tool coolant delivery at 20–80 bar, multi-spindle lathes, internal grinding, gear hobbing and deep-hole drilling requires dosage adjustment because dissolved tramp oil levels above 0.5% by volume increase foam stability and require a stepwise addition of 20% of the starting dose per 0.1% tramp oil increment, up to a maximum of 0.5 wt% concentrate loading. Overdosing beyond this level is associated with filter plugging in 10–25 µm cellulose or polyester mesh filters and with reduced wetting at the tool-workpiece interface in high-pressure operations. Terminal product types include soluble oil emulsions, semi-synthetic coolants, synthetic grinding fluids and heavy-duty forming lubricants; for each, UCON RO-60 is incorporated at the concentrate stage in either a single-screw blending pump or a rotor-stator batch mixer. The polyalkylene glycol structure is preferred where mineral oil defoamers would destabilise the emulsion or where silicone defoamers would create residues on machined aluminium surfaces prior to painting.

    Application areaCompliance instrumentCritical test or operational limit
    Metalworking fluid concentrates and emulsionsASTM D892, ASTM D3601Foam volume ≤50 mL after 5 min; collapse within 10 min
    Alkaline papermaking wet endFDA 21 CFR 176.170, BfR XXXVI/2, EU 2014/687/EUAddition 50–500 g/t dry fibre; maximum white-water COD contribution 50–150 mg/L
    Waterborne industrial coatingsISO 2812-1, Directive 2004/42/ECAddition 0.1–0.6 wt% total formulation; fineness of grind ≤25 µm
    Triethylene glycol natural gas dehydrationASTM D892 modified sparge, GPSA Engineering Data Book Section 20Lean TEG defoamer concentration 10–150 ppmv; reboiler temperature 177–204°C
    High-temperature polyester jet dyeingISO 105-B02, Oeko-Tex Standard 100, ZDHC MRSLDyebath dosage 0.2–0.5 g/L; maximum 0.7 g/L
    Membrane bioreactor aeration basinsOECD 301B, ISO 8192, REACH Annex VIIBasin dosage 1–15 mg/L; maximum 25 mg/L
    Agrochemical suspension concentrates and water-dispersible granulesCIPAC MT 47.3, FAO/WHO specification guidelines, Regulation EC No 1272/2008Formulation dosage 0.05–0.3 wt% in SCs; spray nozzle orifice ≥50 µm

    In alkaline papermaking wet ends where calcium carbonate filler loads exceed 15% of sheet mass, UCON RO-60 is dosed at 50–500 g/t dry fibre, corresponding to 0.005–0.05 wt% on dry furnish, into the fan-pump suction or directly into the white-water return trough ahead of the pressure screen. The use of a polyalkylene glycol synthetic oil defoamer rather than a silicone emulsion is evaluated in mills because silicone carryover can produce fish-eye defects on size-press-treated fine paper and web breaks on single-wire Fourdrinier machines. Compliance for food-contact grades is anchored to FDA 21 CFR 176.170, BfR Recommendation XXXVI/2 and EU Regulation 1935/2004, with migration validation performed under the applicable national reference for food-contact paper and board; for non-food grades, mill environmental discharge limits under EU 2014/687/EU or US 40 CFR 430 govern the final chemical oxygen demand contribution. The downstream production route for high-speed paperboard and tissue includes conical refiner treatment, pressure screening at 0.8–1.5% consistency, dilution to 0.3–0.8% headbox consistency, twin-wire gap forming, wet pressing to 45–50% dry solids, and steam-heated cylinder drying. Foam collapsed at the suction side of the fan pump prevents cavitation and preserves basis-weight uniformity; the defoamer is injected continuously with a diaphragm metering pump after dilution at 1:10 in demineralised water. A process conflict occurs when the same wet end uses cationic starch and polyacrylamide retention aids: excess defoamer beyond 500 g/t can deposit on forming fabrics and reduce first-pass retention by 2–5 percentage points, so mill trials are generally run at three dosage points while monitoring white-water turbidity and headbox foam height. Terminal product types include printing and writing paper, coated folding boxboard, tissue, linerboard and release liners; operational boundaries include a maximum white-water chemical oxygen demand contribution of 50–150 mg/L depending on the mill permit and a prohibition on post-dosing after the pressure screen where shear is insufficient for uniform droplet size distribution.

    Why does microfoam persist after high-shear Cowles dispersion of coalescent-containing acrylic latex?

    High-shear incorporation of UCON RO-60 into waterborne industrial coatings is performed at 0.1–0.6 wt% of total formulation, split typically 60% into the pigment grind and 40% during letdown, because coalescent-rich latex media stabilise microfoam with bubble diameters below 50 µm that do not respond to low-shear post-addition. The grinding stage uses a Cowles disperser at tip speeds of 15–25 m/s and a mill-base viscosity of 85–110 Krebs units; the defoamer is added after pigment wetting to avoid competitive adsorption with the chosen polymeric dispersant. Foam control for these formulations is screened using an adapted ASTM D3601 aqueous foam method for pigmented systems, while dry-film performance is verified according to ISO 2812-1 for resistance to industrial liquid exposures, and volatile organic compound limits follow Directive 2004/42/EC Annex IIA for waterborne coatings. In production, letdown is completed in a cylindrical mixing vessel with a paddle agitator at 300–800 rpm, followed by filtration through a 60–100 µm bag filter and application by air-assisted airless spray at 30–60 psi or by curtain coating for flat stock. Terminal product types include acrylic and vinyl-acrylic interior wall paints, polyurethane dispersion wood coatings, waterborne alkyd trim enamels and airless-sprayed anticorrosion primers. A formulation boundary for UCON RO-60 appears in clear polyurethane dispersions where the insolubility of the polyalkylene glycol droplet can reduce gloss if addition exceeds 0.3 wt% or if the defoamer is added at temperatures below 10°C; in those cases, the fineness of grind gauge should remain below 25 µm and the coating should be passed through a 30 µm cartridge before spray application.

    A lean triethylene glycol loop in a natural gas dehydration unit is treated with UCON RO-60 at 10–150 ppmv on lean TEG inventory when condensate carryover and salt deposition raise foam height during nitrogen sparge testing above 50 cm and prolong foam break time beyond 15 s. The defoamer is injected into the lean TEG after the circulation pump discharge or into the reboiler surge tank, not into the rich TEG ahead of the contactor, because the pressure drop across the bubble-cap trays is insufficient to disperse the polyalkylene glycol before TEG enters the contactor. Compliance for gas dehydration foaming is often assessed by a modified ASTM D892 sparge apparatus at 25°C and 90°C; however, published data for UCON RO-60 at reboiler temperatures above 200°C is limited, so thermal stability audits and inert gas blanketing are required before continuous injection. The process itself includes a high-pressure contactor at 20–70 bar, a lean/rich glycol exchanger, a flash tank at 3–5 bar, a reboiler held at 177–204°C to avoid TEG thermal decomposition at 206°C, and a recirculation rate of 2–5 L TEG per kg water removed. Downstream terminal products are pipeline-spec natural gas with a water dew point of ≤ -10°C at 5.5 MPa, and regenerated TEG returned to the contactor. Operational boundaries include the need to remove light hydrocarbons in the flash tank before the reboiler and the incompatibility of overdosed defoamer with carbon filtration units, where oil droplets above 200 ppmv can shorten activated carbon bed life and increase pressure drop across the particulate filter.

    Jet dyeing foam collapse and pump cavitation thresholds during high-temperature polyester exhaust processing

    During polyester exhaust dyeing in high-temperature jet machines with liquor ratios of 1:5–1:8, UCON RO-60 is pre-dispersed at 1:5 in water at 30–40°C and dosed at 0.2–0.5 g/L of dyebath after the pre-scour and rinse but before the disperse dye is added at 40–50°C. Foam collapse inside the expansion chamber is critical because jet nozzle pressures from 0.5–2.0 bar and fabric rope speeds of 200–400 m/min entrain air, and stable foam can cause pump cavitation that reduces circulation flow by 10–20% and produces uneven dye uptake. Compliance for the finished textile is verified against ISO 105-B02 for light fastness and Oeko-Tex Standard 100 Annex 4 for restricted substances, while the formulation itself should be evaluated against ZDHC MRSL limits for wastewater discharge of non-biodegradable defoamer components. The downstream production sequence includes high-shear jet circulation at 98–135°C, pressure reduction, post-scour, reduction clearing with sodium hydrosulphite for azo dyes, and final rinsing. Terminal product types include polyester woven and knitted apparel fabrics, polyester-elastane stretch fabrics, and microdenier sports textiles. Adding UCON RO-60 above 0.7 g/L is not recommended in this configuration because residual polyalkylene glycol droplets can deposit on the heat exchanger surfaces of the jet machine and reduce heating ramp efficiency; conversely, below 0.15 g/L foam breakthrough during the high-temperature plateau may persist in machines with rope speeds above 350 m/min. Published data for UCON RO-60 in jet dyeing systems operating above 130°C is limited, so a dyehouse trial with abbreviated heating ramp and pressure drop logging is required before continuous production use.

    Membrane bioreactor aeration basins treating high-strength food processing effluent are dosed with UCON RO-60 at 1–15 mg/L of basin volume, added continuously via a positive displacement metering pump into the mixed liquor downstream of the fine-bubble diffuser grid. The dose is started at 5 mg/L and adjusted in 2 mg/L steps only when surface foam height exceeds 30 cm or when the MBR suction pressure increases by more than 5 kPa above a clean-membrane baseline. Compliance screening for this application uses OECD 301B for ready biodegradability, ISO 8192 for aquatic toxicity and REACH Annex VII data for industrial water treatment chemicals; discharge permits for residual chemical oxygen demand and total organic carbon typically constrain the defoamer addition to a maximum of 25 mg/L. The downstream process includes pre-screening, equalisation, anoxic denitrification, aerobic nitrification at mixed liquor suspended solids of 6–12 g/L, membrane filtration through hollow-fibre or flat-sheet modules, and return activated sludge recycle. Terminal product types include indirect reuse water, membrane permeate for reverse osmosis feed, and dewatered waste activated sludge for off-site digestion. The use of a polyalkylene glycol defoamer in this biological system requires monitoring of oxygen uptake rate; a drop greater than 15% in specific oxygen uptake rate after dosing indicates that the defoamer is adsorbing onto the floc surface or contributing a readily degradable load that shifts microbial competition. In such events, the feed rate is halved and the basin is re-aerated until the oxygen uptake rate returns to the previous 24-hour moving average.

    Bead mill wetting and spray tank recirculation in high-load suspension concentrates

    At mill-base viscosities above 1,500 mPa·s, UCON RO-60 is introduced into agrochemical suspension concentrate formulations at 0.05–0.3 wt% of the total formulation, typically after the active ingredient and wetting agent are dispersed but before bead milling, so that the defoamer is incorporated under high shear rather than post-added to the finished formulation. The bead milling operation uses zirconia beads of 0.6–1.2 mm at a residence time of 10–20 min, with cooling to maintain mill-base temperature below 45°C; foam generated in the mill chamber raises internal pressure and can reduce throughput by 15–30% if not controlled. Compliance for the finished suspension concentrate is evaluated by CIPAC MT 47.3 for persistent foam and FAO/WHO specification guidelines for formulation uniformity, while container labelling must follow Regulation (EC) No 1272/2008 and residual solvent limits under the relevant marketing authorisation. Downstream production for water-dispersible granules uses a slurry spray dryer at inlet temperatures of 130–180°C and outlet temperatures of 60–80°C, producing granules with 2–4 mm extruded or spherical forms. Terminal product types include fungicide suspension concentrates, insecticide water-dispersible granules, and herbicide high-load suspension concentrates. UCON RO-60 should not be combined with certain cationic adjuvants in tank-mix formulations without first screening for flocculation, because the polyalkylene glycol defoamer may be displaced from the interface by strongly adsorbing cationic surfactants, and the resulting coarse oil droplets can clog spray nozzles below 50 µm orifice diameter.

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    Certification & Compliance
    More Introduction

    UCON RO-60 Polyalkylene Glycol Synthetic Oil Defoamer is supplied as a silicone-free polyalkylene glycol liquid used for foam suppression in synthetic circulating oils, industrial gear oils, high-temperature chain oils, and ester-based compressor lubricants. The product designation places the material in the ISO VG 60 viscosity classification under ISO 3448, corresponding to a midpoint kinematic viscosity of 60 mm²/s at 40 °C and a permitted classification range of 54 mm²/s to 66 mm²/s when measured by ASTM D445. The polymeric structure comprises oxyethylene and oxypropylene repeat units arranged to provide controlled interfacial activity without introducing polydimethylsiloxane. In synthetic lubricant compounding, class-typical starting treat rates range from 0.01 wt% to 0.2 wt% of finished oil mass. The defoamer is commonly added to the base stock before the final viscosity-modifier and additive-integrity checks because its dispersive behaviour depends on bulk oil polarity, temperature, and water content. As a silicone-free composition, the product is used in plants where silicone carryover creates interference with paint adhesion, oxygen sensors, or close-clearance servo-valve surfaces.

    How Does UCON RO-60 Differ from Silicone and Polyacrylate Defoamers in High-Shear Foam Control?

    Foam control in circulating lubrication systems involves two separate processes: breakage of surface foam lamellae and release of entrained air from the bulk oil. Silicone defoamers, typically polydimethylsiloxane droplets, function through very low surface tension near 20 mN/m and can rupture foam films at treat rates as low as 1 ppm to 20 ppm. That potency is accompanied by operational risk: over-dosing can generate a persistent defoamer film on bearing cages, filter media, and sealing faces, and silicone has been implicated in coating defects and oxygen-sensor drift. UCON RO-60 operates in a different solubility regime. In polar synthetic esters, polyglycol fluids, and selected ester-modified hydrocarbon blends, the polyalkylene glycol defoamer disperses without forming the same low-surface-energy silicone film. Foam collapse occurs through localised surface tension gradients and film drainage disturbances, but the product does not deposit as a polydimethylsiloxane layer. The trade-off is that effective treat rates are generally higher than those required for silicone defoamers, and the exact concentration must be established using ASTM D892 foam-sequence testing rather than extrapolated from silicone experience.

    Polyacrylate defoamers differ again in mechanism and failure mode. They act as high-molecular-weight particles that destabilise foam films, but their performance can decline after prolonged passage through high-shear equipment such as gear meshes, rolling-element bearing cages, and high-speed circulation pumps. Shear degradation reduces particle size and interfacial activity, producing batch-to-batch variability in foaming tendency after extended circulation. UCON RO-60, being a polyalkylene glycol, is more shear-stable than many dispersed-particle polyacrylate defoamers. However, its response is not independent of base-stock chemistry. In polyalphaolefin-only systems or highly nonpolar mineral oil systems, phase separation or low-temperature haze may occur because the polyalkylene glycol has limited solubility in nonpolar hydrocarbon matrices. Published compatibility data for this specific configuration is limited; formulators should perform low-temperature storage screening at −20 °C and high-temperature storage screening at 80 °C before commercial use.

    In addition to silicone and polyacrylate defoamers, mineral-oil-based defoamers are sometimes used in industrial oils. Their use in fully synthetic esters or polyglycol-based fluids is limited by solubility and oxidative stability differences. UCON RO-60 is intended for synthetic oil environments where compatibility with polar base stocks is required and where silicone contamination is unacceptable. The distinction is therefore not simply one of chemical identity but of failure tolerance: silicone defoamers are often potent but contamination-prone, polyacrylate defoamers may lose activity under shear, and mineral-oil defoamers may separate in synthetic polar systems. UCON RO-60 occupies the polyalkylene glycol class, in which shear stability and silicone-free composition are primary specification drivers rather than lowest possible treat rate.

    At compounding plants, the material is introduced into the base oil through a dosing skid after the bulk temperature reaches 40 °C to 60 °C. Low-shear impeller speed is maintained near 200 rpm to 400 rpm to avoid local heating. Direct injection into a high-speed fill line without a recirculation loop can produce temporary haze or additive-rich pockets. A 10 µm side-stream filter or a recirculation pump operating at 3 to 5 vessel volumes per hour restores optical clarity before release. In high-speed bearing test rigs used for ASTM D892 qualification, foaming is most severe when water contamination exceeds 500 ppm; therefore the oil batch is dehydrated before final defoamer concentration adjustment. The defoamer is not a desiccant and does not remove water from the finished lubricant.

    Viscosity Grade, Test-Method Matrix, and Batch-Release Boundaries

    ParameterStandard methodClass-typical specification boundary
    ISO viscosity gradeISO 3448ISO VG 60
    Kinematic viscosity at 40 °CASTM D44554 mm²/s to 66 mm²/s
    Foaming tendency and stabilityASTM D892 Sequences I, II, IIISequence II foam stability target ≤ 0 mL; Sequences I and III evaluated at 24 °C
    High-temperature foamingASTM D6082foam stability target ≤ 0 mL
    Air releaseASTM D3427release time dependent on base oil viscosity and defoamer dose
    Water contentASTM D6304< 500 ppm in sealed storage
    Density at 20 °CASTM D4052polyalkylene glycol class range 1.04 g/cm³ to 1.08 g/cm³
    Flash pointASTM D92class-typical above 220 °C

    The numerical suffix 60 in UCON RO-60 is used here as an ISO VG 60 classification reference under ISO 3448, not as a measured lot viscosity. Individual batch certificates should be checked against the relevant release specification because actual kinematic viscosity, water content, and flash point vary between production lots. For foam-control performance, the most relevant primary tests are ASTM D892 and ASTM D6082; air release is evaluated separately by ASTM D3427 because a formulation can pass foam-sequence limits while still retaining entrained air. The test-method matrix therefore distinguishes foam stability at the surface from air-release time in the liquid phase. These are not interchangeable measurements and formulators should not use a single test as a surrogate for the other.

    Storage vessels for UCON RO-60 should be sealed and fitted with desiccant breathers when ambient relative humidity exceeds 60%. Prolonged exposure to moisture can raise the water content above 500 ppm and may produce haze or reduce interfacial activity. The product should not be air-sparged for mixing because oxygen uptake at temperatures above 80 °C accelerates ether-chain oxidation. In synthetic ester formulations, the addition of the defoamer should be checked for compatibility with acidic phosphate ester additives; strongly acidic species can hydrolyse polyglycol ether linkages and reduce defoaming performance. A 30-day storage stability test at 45 °C and a low-temperature haze test at −20 °C are recommended screening procedures. Avoid predilution with low-boiling solvents unless the finished lubricant formulation can tolerate the solvent because residual solvent lowers the flash point and may distort foam-sequence results.

    In synthetic ester compressor oils and industrial gear oils, UCON RO-60 is typically evaluated at 0.03 wt% to 0.08 wt% before final concentration adjustment. In air release-sensitive hydraulic oils tested under DIN 51524-2, the defoamer concentration should be adjusted only after water and entrained air have been removed from the test batch, because emulsified water changes interfacial tension and can mask the true defoamer response. Over-dosing above 0.2 wt% can prolong air release time even when foam stability remains acceptable. The product is therefore not a universal defoamer for all oil formulations; it is best applied in synthetic lubricants that exhibit sufficient base-stock polarity to maintain a stable dispersion of the polyalkylene glycol phase. In nonpolar PAO or mineral oil systems, phase separation may limit utility unless a co-solvent or dispersant package is present.

    For high-temperature circulating systems operating above 120 °C, the defoamer is added after the main antioxidant package has been dissolved and before the final viscosity modifier is introduced. This sequence reduces the risk of local concentration gradients and allows the defoamer to distribute under low-shear mixing. In high-speed gear rigs, foam control in an ISO VG 46 industrial gear oil has been observed to be most repeatable when the defoamer is added before the viscosity modifier; reverse order of addition can produce transient foam instability during qualification. Published data for this specific configuration is limited, so order-of-addition studies should be part of new-formulation qualification. The relevant foam test uses air sparge rates of 94 mL/min in ASTM D892, with Sequence II measured at 93.5 °C to simulate high-temperature operation. After sparging is stopped, foam stability is recorded after 10 min of settling.

    The product is handled under the substance registration requirements of EU REACH as established by EC 1907/2006. For finished lubricants intended for incidental food contact, the end-user must verify the formulated mixture against FDA 21 CFR 178.3570 or the relevant national equivalent. UCON RO-60 does not by itself confer food-grade approval on the finished lubricant. In safety data sheet review, the product is assessed under the Globally Harmonized System for classification and labelling; flash point values above 60 °C do not place the material in the most severe flammability category, but local fire code storage requirements still apply. In applications where a silicone-free, shear-stable defoamer is required and the base stock has sufficient ester or polyglycol character to disperse the additive, UCON RO-60 is screened first at 0.05 wt%, with subsequent comparison of ASTM D892 Sequence II foam stability and ASTM D3427 air release against the target oil specification.