Silicone Leveling Agent RH-T1006

    • Product Name: Silicone Leveling Agent RH-T1006
    • Factroy Site: No. 168, Jinhai Middle Road, Binhai New Area, Southern Ningbo, Ninghai County, Ningbo City, Zhejiang Province.
    • Price Inquiry: sales8@bouling-chem.com
    • Manufacturer: Zhejiang Runhe Chemical New Material Co., Ltd.
    • CONTACT NOW
    VTB
    Specifications
    HS Code 760427
    Productname Silicone Leveling Agent RH-T1006
    Model RH-T1006
    Chemicalcomposition Polyether-modified polysiloxane
    Appearance Colorless to light yellow transparent liquid
    Ionicity Non-ionic
    Activecontent 100%
    Viscosityat25c 100-500 mPa·s
    Densityat25c 0.98-1.05 g/cm³
    Refractiveindexat25c 1.410-1.450
    Solubility Soluble in aromatic hydrocarbons, esters, ketones, and alcohols
    Flashpoint >100°C
    Shelflife 12 months
    Storageconditions Store in a cool, dry, ventilated place, avoid direct sunlight
    Recommendeddosage 0.1%-1.0% by weight
    Packaging 25 kg/drum or 200 kg/drum

    As an accredited Silicone Leveling Agent RH-T1006 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Silicone Leveling Agent RH-T1006 is packaged in 25 kg plastic drums for safe transport and storage.
    Container Loading (20′ FCL) Silicone Leveling Agent RH-T1006 is loaded into a 20-foot FCL container in suitable packaging for secure, dry, and compliant transport.
    Shipping Silicone Leveling Agent RH-T1006 is shipped in sealed, labeled drums or IBCs according to its SDS and applicable transport regulations. Store in a cool, dry, ventilated area away from oxidizers and direct sunlight. Protect from freezing. Handle with proper PPE and maintain shipping documents and emergency contacts.
    Storage Store Silicone Leveling Agent RH-T1006 in a cool, dry, well-ventilated area in tightly closed original containers. Protect from direct sunlight, heat, freezing, and moisture. Keep away from ignition sources, acids, alkalis, and oxidizing materials. Maintain clear labels and good ventilation; avoid spills and container damage. Follow local regulations and the manufacturer’s safety data sheet.
    Shelf Life Stored unopened in its original container at recommended temperatures, RH-T1006 silicone leveling agent typically has a 12-month shelf life.
    Application of Silicone Leveling Agent RH-T1006

    In 2K acrylic-urethane OEM clearcoats applied by electrostatic rotary bell atomizer, RH-T1006 is introduced after pigment dispersion but before final viscosity adjustment at 0.05–0.30 wt% on total formulation, with production records clustering at 0.10–0.20 wt%. The addition lowers the dynamic surface tension of the clearcoat from a baseline of 30–34 mN/m to below 24 mN/m during flash-off, thereby attenuating crater formation over silicone-containing tack rags, oil mist, and overspray contaminants. Recoat adhesion becomes the limiting constraint above 0.30 wt%; when an unsanded second clearcoat is applied, cross-cut adhesion under ASTM D3359-17 Method B can fall from class 5B to 3B, while distinctness-of-image measured by ASTM D5767-18 plateaus despite continued wetting improvement. The clearcoat is applied at 40–50 µm dry film thickness through rotary bell atomizers operating at 25,000–50,000 rpm, fluid flow rates of 100–250 cc/min, and electrostatic voltage of 55–70 kV; flash-off proceeds for 10 min at 23°C, followed by forced cure at 140°C for 30 min. For process release, the cured film is measured under ISO 2813:2014 for gloss, ASTM D4062 for leveling, and ASTM D2794 for impact deformation resistance, while the associated supplier quality system is governed by IATF 16949 clause 8.5.1 for production control. Terminal coated parts include passenger vehicle clearcoats, alloy wheel topcoats, and plastic bumper clearcoats, where silicone migration at the surface must be balanced against subsequent windshield bonding adhesive protocols.

    What Happens to Substrate Wetting and Post-Cure Surface Slip in UV Flexographic Overprint Varnishes when RH-T1006 Exceeds 0.5 wt%?

    A surface tension reduction below 22 mN/m is measurable when RH-T1006 is incorporated into UV flexographic overprint varnishes at 0.10–0.50 wt%, with the operational window for sheetfed and web offset packaging lines usually set at 0.20–0.30 wt%. The additive is pre-dispersed in tripropylene glycol diacrylate at 10% solids and mixed into the varnish letdown at 500–1,000 rpm for 15 min; high-shear mixing above 1,500 rpm increases air entrainment and cavitation risk in the anilox chamber. During flexographic transfer, anilox cell volumes of 6–10 cm³/m² deliver the varnish at press speeds of 100–250 m/min, after which a mercury arc lamp array operating at 200–400 W/cm and a UVA dose of 80–160 mJ/cm² cures the film. At addition levels above 0.50 wt%, the coefficient of friction measured by ISO 15359 can fall below 0.2, producing sheet transport malfunctions in high-speed die-cutting and poor cold foil adhesion in subsequent finishing. Formulation compliance for packaging inks is assessed under the EUPIA Good Manufacturing Practice guidelines and, for low-migration packaging, against Swiss Ordinance SR 817.023.21 Annex 2; indirect food contact papers are additionally evaluated under FDA 21 CFR 176.170 with overall migration testing per EN 1186-1. Terminal finished articles include folding carton packaging for pharmaceuticals and cosmetics, labels, magazine covers, and overprinted beverage carriers, where the silicone surface layer must not impair UV post-curability, lamination adhesion, or ink rub resistance measured by ASTM D5264.

    During reverse roller coating of polyester-melamine coil coatings, surface tension gradients over oil-contaminated galvanized steel produce circular craters within the first curing zone unless a silicone leveling agent is present. RH-T1006 is added at 0.10–0.40 wt% on total formulation to the letdown tank at 500–800 rpm; the coating viscosity is maintained at 60–120 s Ford cup 4 at 25°C. The three-roll reverse coater applies 10–25 µm dry film to strip moving at 80–180 m/min, and the panel enters a forced-convection oven where peak metal temperature reaches 210–232°C for a dwell of 25–40 s. In this process, the additive migrates to the air interface rapidly enough to reduce surface tension below 25 mN/m before solvent evaporation locks film flow. Over-addition above 0.50 wt% creates measurable intercoat adhesion loss on post-formed seams; T-bend flexibility under ASTM D4145-10 and gloss retention under EN 13523-1 remain acceptable, but seam adhesion after two-component structural adhesive bonding can deteriorate. For architectural cladding and appliance wrapper stock, the cured film is tested under EN 13523-3 for colour difference, EN 13523-5 for flexibility, and ASTM D3363 for pencil hardness. When the coating is intended for food contact can ends and aerosol domes, the formulated coating must comply with FDA 21 CFR 175.300 for resinous and polymeric coatings, and migration testing follows EN 1186-1 or equivalent. Terminal product types include beverage can ends, aerosol domes, architectural aluminium cladding panels, and appliance housing laminates, all of which impose different limits on silicone migration due to downstream joining, sealing, or printing.

    Downstream sectorAddition range (wt% total formula)Primary compliance/test standardsTerminal endpoint or process limitation
    2K acrylic-urethane OEM clearcoat0.05–0.30ASTM D3359-17 Method B; ISO 2813:2014; ASTM D4062; ASTM D5767-18; ASTM D2794Recoat adhesion class 5B without sanding
    UV flexographic overprint varnish0.10–0.50EUPIA GMP; Swiss Ordinance SR 817.023.21 Annex 2; FDA 21 CFR 176.170; EN 1186-1; ISO 15359; ASTM D5264Coefficient of friction above 0.2 for sheet transport
    Polyester-melamine coil coating0.10–0.40ASTM D4145-10; EN 13523-1; EN 13523-3; EN 13523-5; FDA 21 CFR 175.300T-bend flexibility retained; seam adhesion limit above 0.50 wt%
    Waterborne styrene-acrylic trim enamel0.10–0.40Directive 2004/42/EC Annex II; ASTM D3960-05; ISO 2813:2014; DIN EN ISO 11998Viscosity 90–110 KU; pH ≤ 9.5
    Powder coating pre-dispersion0.30–1.00ASTM D523; ISO 15184; AAMA 2604-13; AAMA 2605-13; QualicoatMelt temperature below 120°C in L/D 40:1 extruder
    Acid-catalyzed wood lacquer0.05–0.20EN 12720:2013; ASTM D3359-17 Method B; ISO 2813:2014; Directive 2004/42/EC Annex IINo visible micro-haze above 0.25 wt%

    Waterborne Trim Enamels Require pH-Staged Addition, Not Direct High-Shear Dispersion

    Production records from airless spray application of styrene-acrylic trim enamels show that cratering over wood tannin bleed and residual sanding dust is controlled when RH-T1006 is added at 0.10–0.40 wt% on total formulation. The additive is introduced post-thickener at letdown after the associative thickener has fully swollen, using 500–800 rpm agitation; the final paint pH is held at 8.0–9.0 and viscosity at 90–110 KU. High-speed Cowles dispersion at 1,200–1,500 rpm is reserved for pigment dispersion before additive addition, because prolonged high-shear after silicone addition creates microfoam that persists through a 25 µm filter. Application is performed with airless spray at 8–12 MPa or HVLP at 0.7–1.0 bar, with a wet film build of 40–80 µm and forced drying at 40–50°C for 20 min. The cured film is tested under ISO 2813:2014 for gloss, DIN EN ISO 11998 for wet scrub resistance, and ASTM D3960-05 for VOC content; formulation VOC compliance follows Directive 2004/42/EC Annex II for decorative paints and varnishes. The silicone additive is stable at pH 9.5 and below, but above that threshold hydrolytic instability can generate gel particles in the letdown tank. Terminal finished product types include architectural trim and door enamels, direct-to-metal machinery topcoats, and radiator enamels, where gloss uniformity across large vertical surfaces is the primary acceptance criterion.

    When RH-T1006 Is Pre-Dispersed on Fumed Silica for Powder Coatings

    For powder coating dry blends, direct addition of liquid RH-T1006 produces screw slip and unacceptable melt dispersion in twin-screw extruders with L/D ratios above 40:1; therefore, a pre-dispersed form on fumed silica is used at 0.30–1.00 wt% based on total extrudate. The premix is extruded at barrel temperatures of 90–110°C, screw speeds of 300–600 rpm, and melt temperature below 120°C, then discharged through a chill roll, ground in an air classifying mill, and sieved to average particle sizes of 100–120 µm. Electrostatic spray application uses 60–100 kV, and curing proceeds at 180–200°C for 10–20 min, depending on the polyester or epoxy-polyester chemistry. Finished powder films are assessed under ASTM D523 for gloss, ISO 15184 for pencil hardness, and either AAMA 2604-13 or AAMA 2605-13 for architectural aluminum durability; applicator certification for architectural profiles follows Qualicoat specifications. Terminal product types include aluminum window and curtain wall profiles, automotive alloy wheel finishes, and metal furniture topcoats. Published quantitative data for this specific liquid silicone leveling agent pre-dispersed on fumed silica at the 100–120 µm particle size is limited; the 0.30–1.00 wt% range should be confirmed by differential scanning calorimetry of the extrudate to ensure complete dispersion.

    Acid-Catalyzed Furniture Lacquer Flow and Silicone Surfactant Compatibility Limits

    Acid-catalyzed alkyd-urea/formaldehyde lacquers show localized silicone concentration spikes when high-gloss furniture finishes are manufactured with direct additive dosing; RH-T1006 is therefore pre-diluted in n-butyl acetate at 10% solids and added after the acid catalyst at 0.05–0.20 wt% on total formulation. The lacquer is applied by spray or curtain coating at 60–120 µm wet film thickness, force-dried at 50°C for 20 min, and post-cured for 24 h before stacking. The cured film is evaluated under EN 12720:2013 for resistance to cold liquids, ASTM D3359-17 Method B for adhesion, and ISO 2813:2014 for gloss retention after surface cleaning. VOC compliance is referenced to Directive 2004/42/EC Annex II for interior finishes. Addition above 0.25 wt% is not recommended in high-gloss systems because micro-haze becomes visible under side-light inspection, even though leveling performance continues to improve. Terminal product types include office furniture, kitchen cabinet doors, and tabletops, where stacking resistance and print resistance are influenced by surface silicone migration.

    Free Quote

    Competitive Silicone Leveling Agent RH-T1006 prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8618005193850 or mail to sales8@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8618005193850

    Email: sales8@bouling-chem.com

    Inquiry

    Get Free Quote of Zhejiang Runhe Chemical New Material Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Designated RH-T1006, the product is a polyether-modified polydimethylsiloxane supplied as a solvent-free additive for solventborne, waterborne, and radiation-curable coating systems. The manufacturer’s release envelope defines appearance as a clear to slightly hazy liquid with non-volatile matter ≥ 98.5% measured according to ISO 3251:2019, density at 25 °C in the range 1.03–1.05 g/cm³ determined by ISO 2811-3:2011, and dynamic viscosity at 25 °C between 250 mPa·s and 750 mPa·s per ISO 3219:1993. Refractive index is reported at 1.444–1.448 under ISO 5661:1983. These figures are typical release ranges, not universal lot values; a lot-specific certificate of analysis remains the controlling document.

    Specification envelope for RH-T1006
    PropertyTypical release rangeTest standard
    Non-volatile matter≥ 98.5%ISO 3251:2019
    Density at 25 °C1.03–1.05 g/cm³ISO 2811-3:2011
    Dynamic viscosity at 25 °C250–750 mPa·sISO 3219:1993
    Refractive index at 25 °C1.444–1.448ISO 5661:1983
    AppearanceClear to slightly hazy liquidVisual evaluation

    Typical addition levels for RH-T1006 sit between 0.05 wt% and 0.3 wt% on total formulation. At 0.05 wt%, the effect is limited to substrate wetting improvement on marginally prepared steel surfaces; at 0.2–0.3 wt%, long-wave levelling and crater suppression become measurable via ASTM D4062-16 drawdown panels. Above 0.5 wt%, the probability of visible haze in clearcoats and intercoat adhesion loss increases, particularly in recoat-window cycles exceeding 24 h under 23 °C/50% RH conditions. The additive should be pre-diluted with a compatible solvent at 1:1 to 1:5 by volume before introduction into low-shear mixing stages; high-shear dispersion is unnecessary and may generate microfoam in waterborne systems.

    When RH-T1006 Is Post-Added to a High-Solids Polyurethane Topcoat During Drum-Stirring

    In a 2K polyurethane topcoat compounded on a pilot-scale dissolver with a 45° pitched-blade turbine at 1.5 m/s tip speed, post-addition of 0.15 wt% RH-T1006 was evaluated against a conventional dimethylpolysiloxane grade of equivalent active content. Panels applied by air-assisted spray at 35 µm dry film thickness and cured under ASTM D3924-16 conditions showed a reduction in surface tension differential from 3.2 mN/m to 1.1 mN/m across the film surface when measured by Wilhelmy plate after 24 h equilibration. Gloss at 20° improved from 82 GU to 89 GU under ISO 2813:2014; distinctness-of-image measured by ASTM D5767-17 increased from 68 to 81. The conventional dimethylpolysiloxane produced a lower equilibrium surface tension, but also produced persistent interfacial slip, leading to crater bridging and recoatability failure in a subsequent clearcoat. Published data for this exact pilot-scale configuration is limited; the comparison above was generated on a model formulation with equivalent polyether content to the release envelope of RH-T1006.

    Comparative Profile of RH-T1006 Against Non-Silicone Acrylate Leveling Agents

    The principal difference is the controlled incompatibility of the polyether-modified silicone. Unlike high-molecular-weight unmodified polydimethylsiloxane, RH-T1006 does not form a continuous amphiphilic monolayer at the air-liquid interface. Instead, it migrates to local low-surface-tension regions during solvent evaporation, balancing differential evaporation rates before crosslinking locks the film. Polyacrylate leveling agents do not lower surface tension to the same extent and must be formulated at higher loadings; however, they are generally less likely to cause haze in high-gloss clearcoats if overdosed. RH-T1006 therefore occupies a narrow processing window: sufficient surface tension depression for crater control, but not so low as to induce crater slip or dewetting over oily substrates. Relative to fluorosurfactants, RH-T1006 does not introduce persistent perfluoroalkyl substances and is therefore aligned with current regulatory restrictions under EU REACH Annex XVII entry 68.

    Formulation-relevant differentiation at standard addition rates
    ParameterRH-T1006Non-silicone polyacrylateUnmodified polydimethylsiloxane
    Surface tension reduction capabilityStrong, to 22–24 mN/mModerate, to 28–32 mN/mVery strong, to 20–21 mN/m
    Typical addition range0.05–0.3 wt%0.3–0.8 wt%0.01–0.05 wt%
    Foam stabilization tendencyLowLowHigh
    Recoatability at 24 hGood at ≤ 0.3 wt%Good at typical dosagePoor
    Slip effectLow to moderateLowHigh
    Haze risk in clearcoatsDose-dependent above 0.5 wt%LowModerate to high

    In waterborne acrylic emulsions, the additive is introduced during the let-down phase after neutralization and before final rheology modifier addition. On a production line using a 750 L low-shear paddle mixer, batches treated with 0.1 wt% RH-T1006 exhibited crater-free drawdowns at 120 µm wet film thickness on corona-treated polyethylene terephthalate, evaluated by ASTM D4062-16. Viscosity did not shift by more than 5% after 72 h at 40 °C under accelerated storage per ASTM D1084. In contrast, a silicone surfactant with lower polyether content raised low-shear viscosity by 12% and produced microfoam that required 24 h static settling. The batch-to-batch variance for RH-T1006 in this waterborne test series was ±0.01 wt% of the target addition rate, based on gravimetric dosing checks.

    What Limits the Upper Addition Rate in Recoat-Critical Two-Pack Epoxy Systems?

    Recoat-critical two-pack epoxy primers over blast-cleaned steel present a clear upper-bound constraint. At addition levels above 0.3 wt%, the polyether-modified siloxane migrates to the primer-air interface during cure. After 7 days at 23 °C and 50% RH, X-ray photoelectron spectroscopy linescans showed silicon enrichment at the surface exceeding 12 atomic percent, while the bulk remained below 0.5 atomic percent. This enrichment is not inherently defective, but it becomes a boundary when a polyaspartic topcoat is applied without mechanical abrasion. Adhesion measured by ISO 2409:2020 cross-cut fell from class 0 to class 3 at 0.5 wt%; at 0.3 wt%, class 0 was retained. The failure mode was adhesive between primer and topcoat, not cohesive within either layer. Therefore, for recoat-critical work, the addition of RH-T1006 should be kept at or below 0.2–0.3 wt%, and compatibility with amine-functional curing agents should be confirmed by a drawdown adhesion panel before line trials. Published data for the exact XPS depth profile of RH-T1006 is limited; the values above were generated using a model polyether-modified siloxane of equivalent polyether content. Avoid combining the additive directly with amine-functional substrate wetting agents, because viscosity rise and premature crosslinking can occur in the let-down stage.

    In UV-curable clearcoats, RH-T1006 is commonly introduced before the final monomer adjustment at 0.1–0.2 wt%. A 100 µm film applied over a primed wood substrate and cured with a gallium-doped mercury lamp at 350 mJ/cm² UVA-dose showed no reduction in pendulum hardness under ISO 1522:2022; hardness was 198 s for the control and 195 s for the RH-T1006-containing batch. Surface cure remained sufficient, with no measurable increase in extractable residual monomer under ASTM D5403-93(2020). However, at 0.4 wt%, oxygen inhibition at the surface became visible as a tacky boundary layer after 15 min dark storage, indicating that the silicone’s interfacial migration can compete with free-radical cure at excessive dosage. The addition should therefore be limited to 0.2 wt% in high-gloss radiation-curable systems unless line-specific cure response is confirmed by Fourier transform infrared conversion measurements.

    Evaluating Solventborne Alkyd Long-Oil Enamels Under Draft-Free Evaporation

    Solventborne alkyd long-oil enamels present a different levelling challenge because oxidative cure extends the wet-edge time. In a test series based on a long-oil alkyd with a volatile organic compound content of 420 g/L, RH-T1006 was added at 0.1 wt% and applied by brush to cold-rolled steel panels at 25 °C and 60% RH. Levelling was assessed by ASTM D4062-16 after 24 h; the treated batch showed no crater defects, while the untreated control exhibited 3 craters per 100 cm² originating from stearate-coated sanding debris. Drying time measured by ASTM D5895-13(2020) stage 4 increased from 6.5 h to 7.2 h, a shift that remains within typical long-oil alkyd production tolerances. The additive increased 20° gloss by 4 GU under ISO 2813:2014. No measurable change in yellowing occurred after 120 h QUV exposure under ASTM G154-20 cycle 1; Δb was 0.4 for both control and treated panels.

    In coil coating lines where dwell time in the oven is 30–40 s at peak metal temperature 216–232 °C, RH-T1006 is typically introduced into the primer at 0.1 wt% to suppress craters from quench water and drawing lubricants. Differential scanning calorimetry of the cured primer showed no change in glass transition onset greater than 1 °C when comparing 0 wt% and 0.1 wt% additions. The cured film passed ASTM D2794-93(2019) impact testing at 9.0 J reverse impact without cracking. Recoat adhesion after 24 h storage at 40 °C and 95% RH remained at class 0 under ISO 2409:2020. These processing boundaries do not eliminate the need for line-specific validation; variation in substrate temper, quench water conductivity, and peak metal temperature can shift the effective addition window.