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Anhui Liwei Chemical Co., Limited.

RDP for Industrial Flooring Self-leveling

    • Product Name: RDP for Industrial Flooring Self-leveling
    • 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 874732
    Chemical Composition Vinyl acetate-ethylene copolymer
    Appearance White to off-white free-flowing powder
    Bulk Density 400-600 g/L
    Particle Size 80-120 mesh
    Ph Value 6.0-8.0 (10% aqueous solution)
    Thermal Stability Stable up to 200°C without decomposition
    Minimum Film Forming Temperature 0-5°C
    Adhesion Tensile Strength 1.0-2.5 MPa (on concrete substrate)
    Flexural Strength Increases by 20-40% in self-leveling compound
    Water Resistance Retains 70-85% of initial strength after 7 days water immersion

    As an accredited RDP for Industrial Flooring Self-leveling factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Redispersible polymer powder supplied in 25 kg multi-layer paper bags with moisture barrier, ideal for self-leveling industrial flooring formulations.
    Container Loading (20′ FCL) RDP for self-leveling flooring: 25kg bags on shrink-wrapped pallets, loaded into 20′ FCL for safe transport.
    Shipping RDP (Redispersible Polymer Powder) for industrial self-leveling flooring is shipped in sealed, moisture-proof bags or containers to prevent caking. Store in a cool, dry area, away from direct sunlight and humidity. Handle with care to avoid dust exposure, ensuring safe, stable transport.
    Storage Store RDP in a cool, dry, well-ventilated area, away from direct sunlight and moisture. Keep containers tightly sealed when not in use to prevent caking or lumping from humidity. Maintain temperatures between 5°C and 35°C, and avoid stacking excessively to protect packaging. Properly stored, unopened material remains viable for up to 12 months.
    Shelf Life Shelf life: 12 months from production date when stored unopened in original packaging, in a cool, dry place.
    Application of RDP for Industrial Flooring Self-leveling

    In large-area pump-applied cementitious self-leveling underlayment for high-bay logistics facilities, redispersible polymer powder is dry-blended at 2.8–3.5 wt% of total dry mortar before the mixture enters a continuous mixing chamber coupled to a rotor/stator pump with a field output of 20–25 L/min and hose lengths up to 30 m. The RDP grade selected for this use is typically a carboxylated vinyl acetate–ethylene or VAE/VeoVa copolymer with a glass transition temperature near 0–5°C and a minimum film formation temperature at or below 5°C, allowing coalescence at floor temperatures where hydration heat is the only warming mechanism. Under high shear inside the pump, the redispersed polymer increases the plastic viscosity of the paste phase just enough to prevent segregation of the 0.1–0.5 mm quartz sand fraction and bleeding of free water to the surface. Flow retention remains within 135–160 mm on the EN 12706 flow cone at 5 min, while PCE-based superplasticizer at 0.15–0.30 wt% controls water demand and fluidity. The dry blend comprises CEM I 42.5 R at 35–45 wt%, calcium aluminate cement at 5–12 wt%, anhydrite at 5–10 wt%, quartz sand 0–0.5 mm at 40–50 wt%, RDP at 2.8–3.5 wt%, PCE superplasticizer at 0.15–0.30 wt%, polyether siloxane defoamer at 0.05–0.15 wt%, and lithium carbonate accelerator at 0.10–0.20 wt%. Mixing water is held at 20–23 wt%; higher water demand increases surface porosity and delays the safe application of polyurethane or epoxy topcoats. After installation at 3–10 mm, the underlayment must achieve a bond strength of at least 1.0 MPa on C20/25 concrete under EN 1542, with 28-day flexural strength generally falling between 6.0 MPa and 9.0 MPa under EN 13892-2. The terminal product carries racking loads and occasional VNA truck traffic only after residual moisture is confirmed below 2.0 CM-% for non-breathable overlays, otherwise blistering of the topcoat can occur. Polymer film formation at the interfacial transition zone between aggregate and cement paste is the primary mechanism that raises flexural toughness and reduces microcracking during drying shrinkage.

    Test designations and acceptance bands for RDP-modified industrial self-leveling compounds
    PropertyTest methodIndustrial acceptance bandRDP-related failure mode
    Flow retentionEN 12706135–160 mm at 5 minHigh polymer dose increases plastic viscosity and drops flow below 130 mm
    Bond strengthEN 15421.0 MPa on C20/25 concreteIncomplete film formation below 5°C reduces interfacial polymer bridging
    Flexural strengthEN 13892-26.0–9.0 MPa at 28 dOverdose above 4.5 wt% entrains air and lowers density
    Abrasion resistanceEN 13892-3≤ 10 cm³/50 cm² for heavy trafficNon-coalesced powder increases surface dusting
    Compressive strengthEN 13892-2C25–C40 at 28 dExcess RDP replaces hydraulic binder and suppresses early strength

    What Limits RDP Dosage in Calcium Sulfate-Based Industrial Screeds?

    In calcium sulfate-based self-leveling screeds placed over load-bearing floors in dry production halls and industrial administrative zones, RDP is charged at only 1.5–2.5 wt% of dry mix because the colloid-stabilized latex can retard alpha-hemihydrate and anhydrite hydration when overdosed, producing a softer surface and extending set time beyond site tolerances. The binder phase typically contains 40–55 wt% alpha-CaSO4·0.5H2O or synthetic anhydrite, 35–45 wt% quartz sand 0–0.5 mm, 2–6 wt% Portland cement or hydrated lime for pH adjustment, 0.05–0.15 wt% potassium sulfate or aluminum sulfate accelerator, 0.10–0.25 wt% PCE superplasticizer, and 0.03–0.10 wt% defoamer. RDP modifies the otherwise brittle sulfate matrix by forming polymer bridges between gypsum crystals after drying, which raises 28-day flexural strength from roughly 5.0 MPa for unmodified formulations to 8.0–10.0 MPa under EN 13892-2. Above 2.5 wt%, entrained air rises to 6–10 vol%, compressive strength drops by 15–25%, and drying shrinkage can increase because polymer-stabilized air voids reduce capillary transport through the screed. Placed at 2–5 mm with a pin rake and de-aerated with a spiked roller, the mortar must comply with EN 13813 as CT-C25-F6 or CT-C30-F7 depending on traffic, with surface hardness measured by EN 13892-6. The substrate must be primed on concrete with residual moisture below 0.5 CM-% for calcium sulfate systems, and the terminal floor covering is typically PVC sheet, linoleum, or LVT in dry industrial offices and stores. Wet-process zones are excluded because calcium sulfate loses strength under sustained moisture, regardless of polymer modification.

    On steel-troweled concrete substrates prepared by captive shot blasting to a surface tensile strength of at least 1.5 MPa, bonded self-leveling wear toppings are formulated with RDP at 3.0–4.5 wt% to resist point loading from hard-wheeled forklifts and steel-wheeled trolleys. The dry mix uses CEM I 52.5 R at 25–35 wt%, silica fume at 3–6 wt%, corundum 0.3–1.6 mm at 15–25 wt%, quartz sand 0.1–1.0 mm at 25–35 wt%, PCE superplasticizer at 0.20–0.35 wt%, defoamer at 0.10–0.20 wt%, RDP at 3.0–4.5 wt%, and water demand held at 12–15 wt% because the coarser wear aggregate reduces the free-water requirement. The higher RDP dose forms a thicker coalesced film around the corundum particles, improving impact resistance and crack-blocking between wear aggregates; however, the flow cone value is deliberately reduced to 130–150 mm under EN 12706 to keep corundum from settling during placement. The material is pumped or bucket-mixed and applied at 6–12 mm, then sealed with a solvent-free polyurethane topcoat after the residual moisture falls below 2.0 CM-%. The terminal product is a jointless industrial floor in assembly bays and maintenance aisles, where abrasion resistance tested by EN 13892-3 must remain below 10 cm³/50 cm² for heavy traffic. Substrate cracks narrower than 0.3 mm are pre-filled with an epoxy bridging primer; moving cracks above this width exceed the crack-bridging capacity of the cemented wear layer and require mechanical repair before the topping is placed.

    Bonded Wear Toppings on Steel-Troweled Concrete Demand RDP Dosages Above 3 wt%

    The addition of RDP above 3 wt% in bonded wear toppings is not simply a flexibility adjustment; it changes the failure mode of the topping under dynamic edge loading. Below 3 wt%, the cement matrix near a 0.3–0.6 mm quartz particle remains brittle, and repeated wheel loads initiate radial microcracks that propagate to the wearing surface as dusting or edge spalling. At 3.0–4.5 wt%, the redispersed polymer forms a continuous secondary phase in the capillary pores after coalescence, increasing the critical strain energy release rate at the aggregate–paste interface. This effect is measurable as a 20–40% increase in flexural toughness under EN 13892-2 when compared with an unmodified control at equivalent water-cement ratio. Production-scale mixing requires a compulsory pan mixer with a mixing time of 120–180 s after dry blending, because the polymer powder must be uniformly distributed before the low water content is introduced. The terminal industrial floor is typically a 6–12 mm monolithic surface capable of accepting 150–250 point loads per m² in assembly bays, but the system boundary excludes direct steam cleaning above 60°C because the polymer phase softens and surface hardness under EN 13892-6 may drop below the specified class for thermoset wear surfaces.

    When Ambient Temperature Falls Below 10°C During Large-Area Placement

    In heated but incomplete warehouse slabs placed during winter months, the performance of RDP-modified self-leveling underlayment is controlled by the relationship between the polymer minimum film formation temperature and the wet-mortar surface temperature during the first 24 h. A carboxylated VAE/VeoVa RDP with an MFFT of 4–6°C and a glass transition temperature near 0°C is selected for this exposure because the polymer must coalesce under the low heat output of cement and calcium aluminate hydration. If the slab surface remains below 10°C, coalescence is incomplete and the dried polymer remains as discrete domains rather than a continuous network, reducing surface tensile strength, dust resistance, and the bond to polyurethane or epoxy topcoats. The dry mortar is mixed with 20–22 wt% water preheated to 20–25°C, and calcium formate accelerator is added at 0.3–0.6 wt% to maintain initial set within 90–120 min at the cold substrate temperature. Flow retention after 30 min must remain at least 130 mm under EN 12706, because the cold concrete withdraws water from the wet layer and stiffens the mix before spike rolling is complete. RDP dosage is held at 3.0–4.0 wt%, with pre-dispersion in water for 60–90 s before dry mix addition when the site water temperature is below 15°C. The terminal product is a 4–8 mm underlayment beneath a cold-storage epoxy, where thermal cycling from −30°C to +20°C demands low-temperature flexibility and a bond strength above 1.0 MPa under EN 1542 after 7 d at 5°C.

    Rapid-return refurbishment of food-processing walkways uses a calcium aluminate cement-rich self-leveling repair mortar with 2.0–2.5 wt% RDP to maintain adhesion under 8–12 h reopening schedules. The dry blend contains calcium aluminate cement at 20–30 wt%, OPC at 5–10 wt%, alpha-hemihydrate at 5–10 wt%, quartz sand 0–0.5 mm at 45–55 wt%, lithium carbonate at 0.05–0.15 wt%, PCE superplasticizer at 0.20–0.30 wt%, defoamer at 0.05–0.12 wt%, and RDP at 2.0–2.5 wt%. The polymer powder is incorporated into the dry blend in a compulsory mixer for 60–90 s before water addition to prevent the formation of polymer lumps that would otherwise remain as soft spots after hydration. The mixed material is placed at 5–10 mm, rodded, and finished with a flat trowel to break surface bubbles before the rapid-set exotherm accelerates skin formation. RDP restores interfacial bond strength after substrate preparation by grinding or captive shot blasting, with a minimum 1.0 MPa bond under EN 1542 expected before the 12 h mark. Unmodified calcium aluminate repair mortars under the same schedule often show pronounced tensile surface cracking from rapid exothermic hydration; the polymer phase reduces this by bridging early-age shrinkage cracks and lowering the early modulus of the paste. The terminal product is a standing surface under polyurethane sealers in meat, dairy, and bottling halls, where cleaning agents include dilute sodium hydroxide and hypochlorite. Published data for long-term chemical exposure specific to RDP-modified calcium aluminate self-leveling mortar at pH above 12 is limited.

    Moisture-Barrier Screeds Over Concrete Slabs Without Surface DPM

    In refurbishment of older industrial slabs with residual construction moisture, RDP-modified self-leveling screeds are placed at 3–6 mm over a liquid-applied epoxy moisture-control primer to isolate residual alkalinity and dampness from the new wearing layer. The RDP dosage is set at 3.0–3.5 wt%, because the coalesced polymer film increases adhesion to the epoxy primer through mechanical anchoring into its broadcast sand layer and reduces the risk of blistered delamination from rising vapour. The dry mix includes CEM II/A-LL 42.5 R at 35–40 wt%, quartz sand 0–0.5 mm at 45–50 wt%, PCE superplasticizer at 0.15–0.25 wt%, defoamer at 0.08–0.15 wt%, and RDP at 3.0–3.5 wt%, with water demand at 19–21 wt%. Flow must stay between 135 mm and 150 mm under EN 12706 after 5 min to avoid telegraphing the primer profile through the thin layer. After 28 d, the system must meet EN 13813 CT-C30-F7 for strength and withstand surface pH 12–13 without delamination. The terminal products include vinyl safety flooring in inspection areas and static-control tile in electronics repair workshops, where the self-leveling layer provides both levelling tolerance and a stable alkaline substrate for the final covering.

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    Certification & Compliance
    More Introduction

    RDP-ISF 402 is a redispersible polymer powder based on a carboxylated vinyl acetate–ethylene copolymer. The product is designed for dry-blend incorporation into cementitious self-leveling floor screeds and industrial underlayments. It is produced by spray drying of an aqueous polymer dispersion onto a polyvinyl alcohol protective colloid system selected for compatibility with Portland cement and ternary binder matrices. The dry powder is supplied as a free-flowing white to off-white solid with the specification listed in Table 1.

    Parameter Method Specification
    Chemical base Carboxylated vinyl acetate–ethylene copolymer
    Solids content ISO 3251:2019 ≥98.0 % by mass
    Ash content ISO 3451-1:2019 12 ±2 % by mass
    Bulk density ISO 60:1977 450–650 g/L
    pH of 10 % redispersion ISO 976:2013 7.5–9.5
    Minimum film formation temperature ISO 2115:2000 ≤5 °C
    Residue on 160 µm sieve ISO 3310-1 ≤2.0 % by mass
    Median particle diameter ISO 13320:2020 25–45 µm

    The powder is compatible with calcium aluminate cement and ordinary Portland cement mixtures when the wet slurry pH remains above 9.0. In a 250 kg forced-action batch, pre-blending for 12 min at 40 rpm reduces agglomeration before water introduction. Wet mixing for 90 s at 300 rpm followed by 30 s at 150 rpm produces a flowable slurry without excessive air entrainment.

    How is RDP-ISF 402 Distinguished from EVA and Acrylic Powders in Cementitious Self-Leveling Mortars?

    Commercial redispersible polymer powders for self-leveling formulations are usually classified as vinyl acetate–ethylene, ethylene–vinyl acetate, or acrylic and styrene-acrylic types. RDP-ISF 402 differs from conventional EVA powders in its carboxylated polymer backbone, which provides stronger interaction with calcium ions and mineral fillers during film formation. Compared with acrylic powders, the vinyl acetate–ethylene chemistry produces a softer film at ambient temperature but lower water demand in the wet mortar state. Table 2 shows representative comparative values generated in a CEM I 42.5 R control mix at 3.0 wt% polymer addition.

    Property at 3.0 wt% addition Test method RDP-ISF 402 Conventional EVA RDP Acrylic RDP
    Water demand for 145 mm ring flow EN 1015-3 18.5–21.5 % 20.0–24.0 % 22.5–26.0 %
    28 d flexural strength EN 13892-2 6.5–8.0 MPa 5.5–7.0 MPa 5.0–6.5 MPa
    Pull-off adhesion on concrete EN 1542:1999 0.9–1.5 MPa 0.6–1.0 MPa 0.7–1.2 MPa
    Minimum film formation temperature ISO 2115:2000 ≤5 °C 0–10 °C 0–8 °C
    7 d film hardness Pendulum damping Moderate Low to moderate High

    For plant-scale mixing, the recommended dosage in self-leveling floor compounds is 1.5–4.5 wt% of the total dry mortar mass. Dosages near 1.5 wt% are acceptable for non-structural renovation underlayments. Higher dosages from 3.0 wt% to 4.5 wt% are commonly applied where pallet truck traffic, fork impact, and continuous abrasion are specified. At 2.5 wt% addition, production-scale calibration trials show a flow-ring spread of 145 ±5 mm according to EN 1015-3 when the water demand is set between 18.5 % and 21.5 % depending on the coarse filler fraction. Water additions above 23 % reduce 28 d compressive strength below 20 MPa in CEM I 42.5 R control formulations.

    Water Demand, Flow Retention, and High-Traffic Abrasion Resistance

    The primary technological effect of RDP-ISF 402 in self-leveling systems is a reduction in water demand while retaining pumpable flow and low thixotropy. At 2.5 wt% addition, the apparent viscosity at 10 s⁻¹ measured with a coaxial cylinder rotational rheometer at 23 °C is typically 1.8–2.4 Pa·s. An unmodified control at the same water addition shows 3.1–3.8 Pa·s. The yield stress remains below 15 Pa during the placement interval. This allows pumping through 25 mm and 35 mm internal diameter hoses without segregation of the fine polymer fraction.

    Abrasion resistance measured according to EN 13892-4 shows a 35–50 % reduction in wear depth at 7 d relative to an unmodified formulation. The result is relevant for high-bay warehouses and assembly areas exposed to continuous forklift traffic. Compressive strength development at 24 h is retarded by no more than 15 % at dosages up to 3.0 wt%. At 4.5 wt%, early strength may be reduced by 20–25 %; correction with calcium formate or lithium carbonate is necessary when early opening is required.

    When Damp Concrete Substrates Limit Tensile Adhesion

    Tensile adhesion is measured by pull-off according to EN 1542:1999. On concrete substrates with moisture content below 4 % by the carbide method, RDP-ISF 402 at 3.0 wt% gives adhesion values between 0.9 MPa and 1.5 MPa, with failure predominantly within the screed or substrate. At substrate moisture above 4 % or on old concrete with laitance, the surface requires mechanical preparation by shot blasting or vacuum-assisted diamond grinding. Without preparation, adhesion may fall below 0.5 MPa. On oil-contaminated slabs, a polymer dispersion primer is required before screed application.

    This limitation is common to cementitious self-leveling materials, but the carboxylated polymer film is more sensitive to unreacted lime bloom than conventional EVA powders. In comparative pull-off tests on damp concrete slabs, RDP-ISF 402 retains 0.8–1.0 MPa after 24 h capillary soak, while a conventional EVA powder drops to 0.5–0.7 MPa under the same condition.

    RDP-ISF 402 is compatible with CEM I, CEM II, and calcium aluminate cement blends where the final slurry pH after mixing remains above 9.0. Acidic additives that lower pH below 6.5 should be avoided because the protective colloid loses stabilizing capacity and the redispersed particles agglomerate. Amine-based setting accelerators may interact with the carboxyl groups and generate an increase in viscosity during the first 90 s; formate-based accelerators are preferred. For anhydrite and calcium sulfate flowing screeds, published data for this specific configuration is limited. Preliminary compatibility testing in ternary binder systems is required before specification. The powder is an additive and is not intended for use as a sole binder.

    Storage in unopened bags at 20 °C and relative humidity below 60 % is stable for 12 months. If bags are opened at relative humidity above 60 %, the material should be resealed or consumed within 24 h because moisture uptake increases dust cohesion and reduces flow retention. Silos and pneumatic conveying lines should be fitted with filtration systems to control fine particle release during loading.