Silicone Leveling Agent RH-T1045

    • Product Name: Silicone Leveling Agent RH-T1045
    • 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 150625
    Productname Silicone Leveling Agent RH-T1045
    Model RH-T1045
    Productcategory Silicone leveling agent
    Chemicalcomposition Polyether-modified polysiloxane
    Appearance Colorless to light yellow transparent liquid
    Odor Slight characteristic odor
    Activecontent 100%
    Ionicity Nonionic
    Viscosity 100–500 mPa·s at 25 °C
    Density 1.00–1.05 g/cm³ at 25 °C
    Refractiveindex 1.430–1.450 at 25 °C
    Ph 6–8
    Flashpoint >100 °C
    Solubility Soluble in aromatic, ester and ketone solvents; insoluble in water
    Recommendeddosage 0.1%–1.0% by total formulation weight; adjust by trial
    Application Solvent-based coatings, solvent-free coatings, UV coatings and inks
    Storageconditions Store in a dry, ventilated place, away from direct sunlight, at 5–40 °C
    Shelflife 12 months in unopened original packaging
    Packaging 25 kg drum or 200 kg drum

    As an accredited Silicone Leveling Agent RH-T1045 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaging: Silicone Leveling Agent RH-T1045 is supplied in 25 kg plastic drums or 200 kg steel drums.
    Container Loading (20′ FCL) Silicone Leveling Agent RH-T1045 loaded in a 20′ FCL container, properly packaged, palletized if required, and secured for ocean transport.
    Shipping Silicone Leveling Agent RH-T1045 is shipped in sealed, labeled drums or IBCs under ambient conditions. Store in a cool, dry, ventilated area away from sunlight and incompatible materials. Handle according to the SDS, and classify and document per local transport regulations.
    Storage Store Silicone Leveling Agent RH-T1045 in a cool, dry, well-ventilated area away from direct sunlight, heat, sparks, and incompatible materials such as strong oxidizers. Keep containers tightly closed, upright, and clearly labeled. Protect from freezing and contamination. Observe shelf-life and local regulations; consult the SDS for specific handling and storage requirements.
    Shelf Life Shelf life is typically 12 months when stored in the original, unopened container under cool, dry conditions.
    Application of Silicone Leveling Agent RH-T1045

    In a 2K hydroxyl acrylic/melamine solventborne clearcoat applied over waterborne basecoat in an automotive OEM paint shop, RH-T1045 is introduced at 0.08–0.20 wt% based on total clearcoat weight after letdown. Production-scale robotic bell application records indicate that exceeding 0.35 wt% produces intercoat adhesion loss in wet-on-wet basecoat/clearcoat systems when tested according to ASTM D3359-23 method B, and longwave topography worsens when the high-shear mixing step is bypassed. The downstream compliance frame consists of REACH (EC) No 1907/2006 with an SVHC threshold of 0.1 wt% per article, IATF 16949:2016 control plan and PPAP documentation, and volatile organic compound release testing under EU Directive 2004/42/EC; surface acceptance is measured with ISO 2813:2014 for gloss and ISO 15184:2020 for pencil hardness after humidity exposure. The downstream production process uses robotic electrostatic bell atomization at 50–70 kV, a flash-off zone at 21–23 °C and 50–70 % RH, a dehydration oven at 80 °C for 10 min, and final stoving at 140–150 °C for 20–25 min. The terminal finished product type is the clearcoated automotive body panel or painted exterior plastic component such as a bumper fascia or mirror housing. The additive is added under high-shear agitation with agitator tip speed above 5 m/s during co-solvent letdown because localized silicone-rich droplets in low-shear mixing tanks have caused crater halos in the flash-off zone. Published data for this specific configuration is limited; however, the defect does not recur when the addition stream is diluted to 1 % active material in xylene/butyl acetate before dosing.

    What Happens When RH-T1045 Enters a High-Solids Polyester/Melamine Coil Coating at 200 m/min?

    High-solids polyester/melamine coil topcoats are formulated with RH-T1045 at 0.10–0.30 wt% based on total formulation weight in the topcoat, with lower addition in primers at 0.05–0.10 wt% to avoid interference with chrome-free adhesion promoters. The topcoat formulation typically exhibits a low-shear Brookfield viscosity of 2500–3500 mPa·s at 25 °C and an ISO 6 cup viscosity of 80–110 s; RH-T1045 suppresses cratering, telegraphing, and edge withdrawal during reverse roller coater application and early solvent flash. The coating line applies hot-dip galvanized steel strip at 120–200 m/min after alkaline cleaning, rinsing, and chrome-free nanoceramic pretreatment. A peak metal temperature of 215–232 °C is held for 20–35 s, followed by water quench and rewind tension control. Terminal finished products are pre-painted steel and aluminum coil for architectural building envelopes, appliance wrappers, garage door stock, and rainware profiles. Compliance uses EN 13523-1 for specular gloss and color consistency, EN 13523-7 for flexibility and bending, ISO 2409:2013 for cross-cut adhesion, and REACH (EC) No 1907/2006 for SVHC reporting. Operational boundaries include line speeds above 200 m/min, where air entrainment at the steel/rubber backing roll nip increases microbubble formation; if RH-T1045 is used above 0.50 wt%, intercoat adhesion on foamable PVC plastisol backer layers can fall below Gt 1. The silicone additive is not a substitute for defoamer in high-solids coil formulations because low molecular weight polyether-modified siloxanes can stabilize foam at high shear.

    Release propertyTest method / specification
    Specular gloss of topcoatEN 13523-1; 60° value ≥ 85
    Cross-cut adhesion after cureISO 2409:2013; rating ≤ Gt 1
    Flexibility after bendingEN 13523-7; no cracking at 2T
    SVHC declaration thresholdREACH (EC) No 1907/2006; < 0.1 wt%

    When flat-line UV wood coating lines exceed 12 m/min, the interval between roller application and UV crosslinking is too short for surface tension gradients to relax in 100 % solids urethane acrylate topcoats, producing craters, ribbing, or orange peel on sealed oak veneer panels. RH-T1045 is dosed at 0.05–0.40 wt% based on total UV formulation, with production-scale trials consolidating at 0.10–0.20 wt%; addition above 0.40 wt% lowers intercoat adhesion after sanding and recoating from Gt 0 to Gt 2 under ISO 2409:2013, and increases 20° haze measured by ISO 2813:2014 on black glass panels. The regulatory frame for this downstream route includes REACH (EC) No 1907/2006; if the coated component is used in a toy or childcare article within scope of EU Toy Safety Directive 2009/48/EC, migration testing under EN 71-3:2019+A1:2021 is applied to the cured film. The production process consists of a two-roller coater running at 8–15 m/min, followed by 2 × 240 W/cm² mercury vapour lamps and one 395 nm LED array, with radiant exposure controlled at 800–1200 mJ/cm² for the final topcoat. Terminal finished product types are engineered wood flooring, kitchen cabinet doors, desktops, and flat-pack furniture panels. The additive is pre-mixed in the acrylate oligomer under 1500 rpm for 10 min; if wood moisture content exceeds 10 %, the substrate is pre-dried at 45–50 °C for 24 h because RH-T1045 cannot eliminate water-vapor-induced craters in a 100 % solids system.

    When a Waterborne 2K Polyurethane Spray Line Encounters Cratering and Picture Framing

    In waterborne 2K polyurethane topcoats for agricultural and construction machinery, RH-T1045 is added at 0.10–0.30 wt% based on total liquid coating after the acrylic polyol dispersion is pre-emulsified and before isocyanate addition; direct addition into mixed paint with short pot life creates silicone-rich gel particles at the spray nozzle. The downstream production process uses HVLP/AirMix spray equipment at 1.5–2.5 bar atomizing pressure, a target dry film thickness of 60–80 μm, flash-off at 20 °C and 60 % RH for 15 min, then forced curing at 80 °C for 30 min. Compliance for this segment is anchored to ISO 11890-2:2020 for VOC content, ASTM D4060-19 for Taber abrasion resistance, ISO 2813:2014 for gloss, and REACH (EC) No 1907/2006 for SVHC reporting. Terminal finished product types are tractor hoods, combine harvester panels, hydraulic pump housings, and other machine guarding components. Operational boundaries include a pH ceiling of 8.5 in the formulated coating; above this value, polyether-modified siloxane hydrolysis can occur during 6-month storage at 25 °C, producing surface defects that are not present in fresh batches. The additive is not combined with high levels of amine-neutralizing agents above 0.5 wt% on binder solids, because amine-catalyzed isocyanate reactions can alter film formation before the leveling agent migrates to the air-liquid interface.

    Pigmented nitrocellulose-based flexographic ink formulations printed on corona-treated BOPP film at press speeds of 600–800 m/min exhibit ribbing, pinholing, and dot bridging when the ink’s dynamic surface tension remains above the substrate’s wetting envelope during the 50–150 ms residence time between anilox metering and impression nip. RH-T1045 is incorporated into the letdown solvent at 0.20–0.80 wt% based on finished ink weight, with lower doses in high-viscosity gravure inks and higher doses in water-reducible flexo bases; above 0.80 wt%, ink may transfer excessively to the anilox roller and create ghost images on trailing film advance. For food-contact flexible packaging, the ink system must comply with EU Regulation (EC) No 1935/2004, Commission Regulation (EC) No 2023/2006 on good manufacturing practice, Commission Regulation (EU) No 10/2011 for plastic food contact layers including printed surfaces, and EuPIA Good Manufacturing Practices; migration testing follows the applicable worst-case ratio of printed film to food simulant. The downstream process is solvent-based flexographic printing on a central impression press with photopolymer plate mounting, chambered doctor blade anilox metering, and forced-air drying at 60–80 °C in a dryer length of 1.5–2.0 m per color station. Terminal finished product types are snack food wrappers, confectionery overwrap, shrink sleeve labels, and stand-up pouch outer films. The addition stream is pre-diluted to 1 % active matter in ethyl acetate/propyl acetate before mixing to avoid localized low-surface-tension spots that print as halo defects on high-tension films.

    Powder Coating Extrusion Dispersion and Surface Defect Thresholds

    After pre-adsorption onto fumed silica at a 1:1 ratio, RH-T1045 is introduced into thermosetting polyester/β-hydroxyalkylamide and polyester/epoxy hybrid powder coatings at 0.10–0.50 wt% on resin solids. The pre-dispersion step is critical because liquid polyether-modified siloxane injected directly into the premix hopper causes screw slippage and feed surging on a twin-screw extruder with L/D 18:1 and barrel temperatures of 90–110 °C. The downstream powder process includes high-speed premixing at 1500 rpm for 30–60 s, melt extrusion, chill roll cooling, flaking, pulverization to a particle size distribution with D50 between 35 μm and 45 μm, and electrostatic spraying at 60–80 kV onto pretreated aluminum or steel. Cure is performed at 180–200 °C for 10–15 min depending on substrate mass and oven profile. Terminal finished product types are architectural aluminum profiles, domestic appliance panels, and outdoor furniture frames. Compliance for architectural aluminum is governed by the Qualicoat specification for powder coatings, with additional REACH (EC) No 1907/2006 SVHC reporting and RoHS Directive 2011/65/EU restrictions where electrical/electronic equipment housings are coated. Operational boundaries include a maximum dosage of 0.50 wt%; above this level, block resistance under 40 °C aging and intercoat adhesion of reclaimed powder deteriorate, and the electrostatic transfer efficiency decreases because the silicone-rich surface lowers powder cloud conductivity. The addition is not combined with zinc stearate at levels above 0.5 phr in the premix, because combined migration of both surface-active species produces haze bands in the cured film.

    Free Quote

    Competitive Silicone Leveling Agent RH-T1045 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
    Technical profile: Silicone Leveling Agent RH-T1045 is supplied as a clear, colorless to pale yellow liquid based on a polyether-modified polydimethylsiloxane copolymer. The product is intended for solventborne, high-solids, and radiation-curable industrial coatings in which surface-tension-driven defects such as cratering, orange peel, and picture framing require correction without the severe recoatability penalties associated with linear high-molecular-weight dimethylpolysiloxanes. The manufacturer’s quality-control specification lists non-volatile content at ≥ 98 % by ISO 3251, dynamic viscosity at 25 °C between 40 mPa·s and 120 mPa·s using ASTM D2196, density at 20 °C of 0.98–1.03 g/cm³ by ASTM D4052, and refractive index at 25 °C of 1.445–1.455 by ASTM D1218. Gardner color is specified as ≤ 2 per ASTM D1544, and flash point is reported above 100 °C by ASTM D93. The material is soluble in aromatic hydrocarbons, esters, ketones, and glycol ether acetates at 20 °C, while water solubility is below 1 %.
    Quality-control compliance matrix for Silicone Leveling Agent RH-T1045 as supplied
    ParameterTest methodSpecification
    Non-volatile contentISO 3251≥ 98 %
    Dynamic viscosity at 25 °CASTM D219640–120 mPa·s
    Density at 20 °CASTM D40520.98–1.03 g/cm³
    Refractive index at 25 °CASTM D12181.445–1.455
    Gardner colorASTM D1544≤ 2
    Flash pointASTM D93> 100 °C

    What Surface-Tension and Crater-Control Response Is Obtained in Acrylic-Melamine Enamels?

    In a high-solids acrylic-melamine clearcoat applied with a 100 µm wire-wound bar to cold-rolled steel, the addition of 0.3 wt% RH-T1045 on total resin solids reduces equilibrium surface tension from approximately 28 mN/m to 21–23 mN/m as measured by ASTM D1331 at 25 °C. The surface-tension depression is maintained over a dosage range of 0.05 wt% to 0.8 wt%. At higher addition levels, excess surface-active copolymer can accumulate at the air interface and produce haze or silicone-contaminated overspray zones. The polyether chain length of this leveling agent is selected to create a controlled incompatibility window: the molecule migrates rapidly to the coating-air interface during flash-off and crosslinking but does not form discrete silicone domains large enough to function as crater nuclei. In a white high-solids polyester-melamine coating, crater density on a deliberately contaminated panel was reduced from 14 craters/dm² to 0 at 0.2 wt% after 20 min flash-off and 30 min bake at 130 °C. Specular gloss measured by ISO 2813 at 60° geometry remained above 90 GU in the same system.

    Addition Sequence, Dosage Limits, and Solvent Pre-Dilution Protocols

    RH-T1045 is introduced into the letdown phase after pigment dispersion and grind cool-down, typically below 40 °C. Pre-dilution with an aromatic or ester solvent at 1:10 to 1:20 parts by weight is recommended before addition under low-shear agitation at 500–800 rpm in a Cowles dissolver. Addition to the grind phase is not recommended because competitive adsorption on pigment surfaces can reduce the concentration available for the air interface and increase demand by 30–50 %. Dosage ranges from 0.05 wt% to 0.8 wt% on total formulation mass. Levels below 0.05 wt% usually provide insufficient surface-tension depression to close surface gradients across a 200 µm wet film; levels above 1.0 wt% may cause intercoat adhesion loss, silicone overspray contamination, and reduced intercoat wetting in repair operations. In radiation-curable acrylate systems, the preferred addition window narrows to 0.1–0.3 wt% because higher addition rates reduce cure response and surface conversion at the air interface. In coil coating lines running at 60–120 m/min with roto-gravure chrome-plated rolls, RH-T1045 is typically added to the topcoat letdown tank 20–30 min before line start. Batch-to-batch viscosity drift on a high-solids polyester topcoat was measured at ± 3 s Ford Cup 4 at 25 °C when the additive was pre-diluted at 1:15 in butyl acetate and fed by metering pump into the recirculation loop. Direct addition into the vortex of a high-speed disperser without pre-dilution produced localized surfactant-rich droplets that persisted for 15–20 min and appeared as micro-craters on the first 50 running meters of coated coil.

    When Recoatability and Intercoat Adhesion Become Processing Constraints

    Because RH-T1045 migrates to the coating surface during film formation, residual siloxane at the cured interface can reduce the surface energy of the dry film and interfere with subsequent coat-to-coat wetting. In a 2K acrylic-polyol/HDI clearcoat applied over an RH-T1045-containing basecoat, cross-cut adhesion measured by ASTM D3359 method B remained 5B after 24 h of ambient cure when the basecoat addition level was 0.1 wt%. At 0.6 wt%, cross-cut adhesion decreased to 3B, and the recoat surface exhibited visible dewetting after spray application of a second clearcoat layer. Sanding with P600 abrasive and solvent wiping with isopropanol restored adhesion to 4B–5B in the same test series. Recoatability should be confirmed under production conditions whenever addition rates exceed 0.3 wt%; published data for this specific configuration is limited above 0.5 wt%. Foam stabilization is lower than linear polydimethylsiloxane, but high-shear air entrainment in vacuumless spray systems can still produce microfoam. Defoamer selection should be confirmed after addition of RH-T1045; incompatible defoamers can create crater nuclei. Avoid combination with high levels of amine-functional silanes and strongly acidic aqueous systems below pH 4.0, because polyether segments may undergo acid-catalyzed hydrolytic cleavage under extended storage. At relative humidity above 60 %, condensation-induced surface defects may require a slower solvent blend or a high-boiling coalescent; RH-T1045 does not function as a moisture scavenger.

    Thermal Stability and Volatility Limits During Forced Drying

    Thermogravimetric analysis under nitrogen at 10 °C/min indicates 5 % mass loss at approximately 250 °C for the neat additive. In a high-solids polyester-melamine clearcoat, the cured film shows no yellowing at bake temperatures up to 150 °C for 30 min. At 180 °C for 30 min, Delta b by ASTM D2244 increases by 0.8 in a 40 µm dry film. The additive should not be used in systems exposed to sustained service temperatures above 180 °C, because oxidative degradation of the polyether chain may generate volatile degradation products and reduce slip retention.

    Where RH-T1045 Differs from Linear PDMS, Polyacrylate, and Fluorosurfactant Flow Agents

    Compared with a 10,000 cSt linear polydimethylsiloxane, RH-T1045 produces lower equilibrium surface-tension reduction but a wider compatibility window. The linear PDMS can reduce surface tension to 19–21 mN/m at 0.05 wt%, but its low solubility in high-polarity acrylic formulations results in cratering and intercoat adhesion loss at addition rates above 0.05–0.1 wt%. RH-T1045 is soluble in the same acrylic-melamine and 2K polyurethane systems at 0.3–0.8 wt% without visible haze in 40 µm films. Compared with a high-molecular-weight polyacrylate leveling agent, RH-T1045 delivers greater reduction in longwave orange peel and provides slip and mar resistance, whereas the polyacrylate does not reduce the coefficient of friction. Compared with a fluorosurfactant, RH-T1045 does not achieve surface tensions below 20 mN/m on low-energy substrates, but it also does not stabilize foam to the same extent and is less likely to cause wetting defects in the next coat.
    Comparative laboratory screening of flow additives in a 2K acrylic-polyol/HDI clearcoat at 0.3 wt% additive on total resin solids, dry film thickness 45 µm, cure 7 d at 23 ± 2 °C
    ParameterRH-T1045Linear PDMS 10,000 cStPolyacrylate flow agent
    Equilibrium surface tension of liquid coating, ASTM D133122 mN/m20 mN/m27 mN/m
    Wavescan longwave after cure4.15.68.3
    Wavescan shortwave after cure7.214.89.4
    Cross-cut adhesion after recoat, ASTM D33595B2B5B
    Foam collapse time, air-sparge test45 s120 s30 s
    Selection between these chemistries is determined by substrate surface energy, required recoat adhesion, and exposure to high-humidity condensation. RH-T1045 is specified where a balanced profile of surface-tension reduction, intercoat adhesion, and foam control is required in high-solids and 2K polyurethane topcoats.