| HS Code | 125090 |
| Appearance | white powder |
| Bulk Density | 400-600 g/L |
| Average Particle Size | 80-120 µm |
| Ph Value Of Dispersion | 7-9 |
| Ash Content | 10-15% |
| Minimum Film Forming Temperature | 0-5°C |
| Tensile Strength Of Film | 8-12 MPa |
| Elongation At Break | 300-500% |
| Adhesion To Concrete | >1.0 MPa |
| Water Resistance | excellent |
| Redispersibility | excellent |
| Storage Stability | 12 months in dry, cool conditions |
As an accredited RDP for Polymer-modified Waterproofing Coatings factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | RDP supplied in 25 kg moisture-proof laminated kraft bags with inner polyethylene liner, ensuring stable performance in waterproofing coatings. |
| Container Loading (20′ FCL) | 20′ FCL of RDP powder for polymer-modified waterproofing coatings, palletized, shrink-wrapped, and securely loaded for safe transport. |
| Shipping | RDP for polymer-modified waterproofing coatings is shipped in 25 kg kraft paper bags with PE liners. Keep pallets dry and covered during transit; avoid excessive humidity, direct sunlight, and rough handling. Store in a cool, ventilated area. Shelf life is typically 12 months from production date when sealed properly. |
| Storage | Store RDP in a cool, dry, well-ventilated area, away from direct sunlight, heat, and moisture. Keep bags tightly sealed to prevent absorption of humidity and caking. Avoid stacking near openings or damp floors. Recommended storage temperature is below 30°C. Use within 12 months of production for optimal performance in polymer-modified waterproofing coatings. |
| Shelf Life | Shelf life is typically 12 months from manufacture when stored in a cool, dry place away from moisture. |
In below-grade concrete box structures, positive-side waterproofing with a one-component polymer-modified cementitious slurry is generally performed before backfilling. The dry formulation is based on ordinary Portland cement CEM I 42.5 N, graded silica sand 0.1–0.5 mm, and a vinyl acetate-ethylene (VAE) RDP at 5.0–7.5 wt% of total dry batch. At a fixed cement content of 50.0 wt%, the polymer-to-cement ratio lies between 0.10:1 and 0.15:1. This ratio produces a semi-flexible microstructure in which coalesced polymer films block capillary pores after the drying phase but do not form a continuous elastomer network. Compliance for liquid-applied water impermeable products under tile and for cementitious waterproofing slurries is assessed under EN 14891:2017; where the coating is supplied in China, GB/T 23445-2009 Type I criteria are commonly referenced. Adhesion is verified according to ASTM D4541-17 on concrete slabs cured 28 days and prepared by mechanical grinding to remove laitance. Dry-mix production uses a twin-shaft compulsory mixer with plough blades rotating at 15–18 rpm and side choppers at 1500 rpm. The RDP is metered through a feed screw at a rate of 25–35 kg/min, and the blend is kept below 40°C because VAE powders with glass transition temperatures below 5°C can soften under frictional heat and form deposits on discharge gates. Residual moisture is controlled below 0.3 wt% before bagging in 25 kg valved polyethylene-lined bags. On the construction site, the powder is mixed with clean water at a water-to-powder ratio of 0.22–0.26 in a low-speed paddle mixer at 350–450 rpm. The mixing sequence is 3 min initial dispersion, 2 min slaking, and 30 s re-stir. Application is made by stiff nylon brush, rectangular steel trowel, or airless spray in two passes, achieving a total dry film thickness of 1.2–1.5 mm. Curing begins with 48 h moist protection, followed by 7 days at 20–25°C and 45–65% RH. Terminal finished product types in this segment include one-component brush-grade tanking slurry, trowel-grade positive-side waterproofing mortar, and roller-applied basement slurry supplied to contractors as bagged goods. The main process conflict is that early drying at RH below 40% before 72 h causes surface shrinkage cracks, while continuous wet curing past 7 days can delay film coalescence and reduce hydrostatic pressure resistance.
Crack-bridging response in thin-bed polymer-modified cementitious under-tile waterproofing is not linear when the RDP addition crosses the 15 wt% threshold. At 12 wt% of total dry mix, the redispersed polymer phase occupies capillary pores and interfacial transition zones, but crack openings of 0.2–0.3 mm can propagate without continuous film stretching. At 18–20 wt%, the polymer-to-cement ratio reaches 0.45–0.50:1 when the cement content is fixed at 40.0 wt%, producing a co-continuous VAE film that can bridge static cracks up to 0.4 mm at 23°C under EN 14891:2017 test conditions. Compressive strength declines from roughly 18–22 MPa at 12 wt% to 10–14 MPa at 18 wt%, which is acceptable for bonded waterproofing membranes but not for load-bearing structural repair. Under-tile balcony and wet-room membranes in the EU are assessed against EN 14891:2017, with adhesion after water immersion and heat ageing checked by ASTM D4541-17. For Chinese market formulations, GB/T 23445-2009 Type II flexural requirements may be referenced. Production-scale dry blending uses a horizontal ribbon mixer with a 60–65% fill level and a mixing time of 240 s at 20 rpm. RDP is pre-dispersed with silica sand for 90 s before cement is added, because direct co-mixing of RDP with cement in high-shear zones can generate powder agglomerates that later appear as uncoalesced white streaks in the cured membrane. On manufacturing lines, batch-to-batch variance in RDP moisture content above 1.0 wt% has been observed to reduce metering screw discharge accuracy by 4–6%, requiring conditioned conveying air at 25–35°C and a dew point below -10°C. The wet preparation on site uses a water-to-powder ratio of 0.20–0.24 and a two-speed drill mixer operating at 600 rpm for 2 min; high-shear dispersion is necessary to fully redisperse the powder, but overtempering beyond 4 min can damage air-entraining components and entrain excessive air, reducing water impermeability. The membrane is applied in two coats at 0.8–1.0 mm wet film per coat, with the second coat at right angles after the first coat reaches 4–6 h at 20°C. Finished products generated by this route include one-component flexible cementitious under-tile waterproofing membrane, balcony and wet-room waterproofing slurry, and brush-applied crack-bridging coating for renovation over existing rigid substrates. A process limitation is that crack-bridging performance is strongly reduced when the membrane is applied at wet-film thickness below 0.6 mm per coat or when the substrate is exposed to forced drying at RH below 35% during the first 72 h. Published data for specific RDP grades in cyclic crack movement beyond 0.5 mm is limited, requiring formulation-specific test panels.
| RDP addition (wt% of total dry mix) | Polymer-to-cement ratio (fixed 40.0 wt% cement) | 28-day compressive strength (MPa) | Static crack bridging at 23°C (mm) | Water impermeability response |
|---|---|---|---|---|
| 8 | 0.20:1 | 24–28 | 0.1–0.2 | Passes 0.3 MPa hydrostatic pressure; visible stress whitening at 0.2 mm |
| 12 | 0.30:1 | 18–22 | 0.2–0.3 | Passes 0.3 MPa hydrostatic pressure; limited crack bridging |
| 18 | 0.45:1 | 10–14 | 0.4–0.5 | Passes 0.3 MPa hydrostatic pressure; co-continuous polymer film |
| 22 | 0.55:1 | 6–9 | 0.5–0.7 | Passes 0.3 MPa hydrostatic pressure; abrasion resistance reduced under ASTM D4060-19 |
On exposed roof decks subject to pedestrian traffic, freeze-thaw cycling, and standing water, the dry formulation is adjusted to 22–28 wt% RDP of total dry batch, corresponding to a polymer-to-cement ratio of 0.55–0.70:1 at a cement content of 40.0 wt%. This level moves the cured layer from a rigid coating into an elastomeric membrane, with elongation at break typically in the 30–60% range under 23°C tensile loading. Compliance for cold liquid-applied elastomeric waterproofing membranes with integral wearing surfaces is evaluated under ASTM C836-18, while surface protection criteria follow EN 1504-2:2004. Abrasion resistance is assessed by ASTM D4060-19 using a Taber abraser with CS-17 wheels and a 1000 g load; wear index values above 2.0 g/1000 cycles generally require the addition of 0.5–0.8 mm quartz aggregate broadcast onto the wet first coat. Dry-mix production for such high RDP loadings requires a jacketed ribbon blender or a ploughshare mixer with temperature control. Frictional heat from mixing at 25 rpm can raise the powder bed above 45°C within 180 s if the cooling jacket is not activated. Processing in hot weather above 35°C requires chilled water at 5–15°C during site mixing and storage of bags in shaded areas. The site-mix protocol uses a high-shear forced-action mixer with a water-to-powder ratio of 0.20–0.23 and a rotor-stator dispersion tool at 800 rpm for 3 min; the resulting viscosity should be in the range of 60,000–85,000 mPa·s at 20°C for roller application. Spray application through a worm-pump continuous mixer with a 6–8 mm nozzle orifice delivers a wet-film thickness of 1.5–2.0 mm per pass. After the first pass, 0.5–0.8 mm quartz aggregate is broadcast at a rate of 2.5–3.5 kg/m² to provide pedestrian slip resistance. The second pass locks the aggregate. Curing requires 48 h moist protection and 10 days at 20–25°C and 50–60% RH. Terminal finished product types from this segment are roof-deck pedestrian traffic membranes, anti-slip cementitious waterproofing coatings, and spray-applied balcony/terrace membranes. The primary operational boundary is freeze-thaw: the glass transition temperature of the selected RDP must be at least 15°C below the lowest anticipated service temperature, and wet-film frost exposure before 72 h can lead to irreversible loss of elongation and surface cracking.
Potable-water tank linings based on RDP-modified cementitious mortars require a different dosage ceiling than external waterproofing because organic migration from the polymer film must remain below the thresholds set by certification bodies. The addition ratio is commonly held to 6–10 wt% of total dry batch, producing a polymer-to-cement ratio between 0.15:1 and 0.25:1 at a cement content of 40.0 wt%. Compliance must be established on the final cured formulation under NSF/ANSI/CAN 61 or AS/NZS 4020:2018; in the European market, the applicable drinking water regulation EU 2020/2184 may require Member State-specific approval for site-applied linings. RDP selection is restricted to grades with low residual vinyl acetate monomer below 10 ppm and low alkylphenol ethoxylate content. Production of the dry-mix uses a stainless steel horizontal mixer with 12–15 rpm blade speed and a jacket temperature below 35°C. The powder is bagged in food-grade paper-valve bags with a PE inner liner. On-site mixing uses a rotor/stator continuous mixer with water conforming to EN 1008:2002, at a water-to-powder ratio of 0.22–0.26. The lining is applied by airless spray or trowel to a total dry thickness of 2.0–3.0 mm in two or three coats. Curing is prolonged: 14 days moist curing at 15–25°C followed by 14 days dry aeration at 20–25°C and 50–65% RH before any water contact. This schedule reduces vinyl acetate hydrolysis products and residual surfactant leaching. Finished goods in this segment include trowel-applied reservoir lining mortar, spray-applied cementitious tank lining, and ready-to-use repair mortar for concrete potable water structures. A critical operational boundary is that published data for specific RDP grades in potable water organic migration is limited, and each final formulation must be subjected to full extraction testing; lowering the RDP dosage below 6 wt% improves leaching results but reduces crack-bridging capacity below 0.2 mm.
Sulfate-bearing effluents in industrial sumps attack cementitious waterproofing layers through ettringite expansion and gypsum softening. RDP modification at 8–12 wt% of total dry batch reduces liquid ingress and thereby limits sulfate ion diffusion, but it does not make the lining chemically resistant to strong mineral acids. At 12 wt%, the polymer-to-cement ratio is 0.30:1 when the cement content is 40.0 wt%. This ratio forms a dense polymer-cement co-matrix that lowers capillary absorption by 40–60% compared with an unmodified mortar under ASTM C1585-20 measurement. Sulfate resistance is assessed by ASTM C1012/C1012M-18 using 50 g/L sodium sulfate solutions; expansion limits are typically set at 0.10% at 6 months. Chemical resistance of the cured lining is evaluated by ASTM C267-20 after immersion in 5% sodium sulfate and 0.5% sulfuric acid. The production line uses a twin-shaft compulsory mixer with a 20 rpm main shaft and a 180 s dry-blend cycle; the RDP is introduced after 45 s of pre-mixing cement and sand to prevent powder segregation. The site mix is prepared with a water-to-powder ratio of 0.24–0.28 and a low-shear paddle mixer at 400 rpm for 3 min; the mortar is then applied by flat trowel at 2.0 mm total thickness over a saturated-surface-dry concrete substrate. Curing is conducted at 20–25°C for 7 days under polyethylene sheeting, with a further 7 days ventilated at 50–65% RH. Downstream packaged forms in this segment are sulfate-resistant sump lining mortar, effluent channel waterproofing coating, and chemically resistant polymer-cement resurfacing mortar. The operational boundary is that RDP-modified cementitious linings are unsuitable for continuous immersion in mineral acids below pH 3, organic solvents, or hot alkaline streams above 60°C; those environments require epoxy or vinyl ester systems instead.
Between tide levels, polymer-modified cementitious repair mortars are used as waterproofing and chloride-barrier layers on concrete elements that alternate between saturated and rapidly drying conditions. The RDP addition is held to 4–6 wt% of total dry batch to retain compressive strength above 30 MPa while reducing permeability. At 5 wt% and a cement content of 45.0 wt%, the polymer-to-cement ratio is 0.11:1. Compliance for structural repair mortars follows EN 1504-3:2006 class R3 or R4, while the waterproofing function is assessed under EN 1504-2:2004; adhesion is measured by ASTM D4541-17 after 7 days moist cure and 21 days ambient cure. The dry blend is manufactured in a planetary counter-current mixer at 35 rpm for 300 s, with all powders dried to 0.2 wt% moisture before mixing. Site application requires a paddle mixer at 300–400 rpm and a water-to-powder ratio of 0.16–0.20. The repair mortar is applied by trowel in 10–20 mm lifts onto a pre-wetted substrate with roughness of at least 1.5 mm Rz. The lower RDP dosage produces a mortar with greater stiffness than flexible membrane products; therefore, it is not intended for crack bridging beyond 0.2 mm. The core technical conflict in splash-zone curing is that cement hydration requires near-saturated conditions for the first 7 days, while latex film coalescence requires progressive drying. If the mortar is exposed to salt spray and direct sun within 24 h, the polymer film fails to coalesce and the surface can lose 20–30% of adhesion measured by pull-off. The segment yields polymer-modified cementitious repair mortar for splash zones, chloride-resistant waterproofing mortar for marine infrastructure, and high-build patching mortar for concrete repair. The operational boundary is that application below 5°C or above 35°C significantly extends the time required for film coalescence and increases the risk of surface cracking before the polymer phase develops.
| Application sector | RDP dosage (wt% of total dry mix) | Primary standard | Critical process control point | Terminal product type |
|---|---|---|---|---|
| Positive-side basement tanking | 5.0–7.5 | EN 14891:2017 / GB/T 23445-2009 | Moisture ≤ 0.3 wt% before bagging | One-component tanking slurry |
| Under-tile balcony membrane | 18–20 | EN 14891:2017 / ASTM D4541-17 | Wet-film ≥ 0.6 mm per coat | Flexible cementitious membrane |
| Roof-deck traffic coating | 22–28 | ASTM C836-18 / EN 1504-2:2004 | Mix temperature < 45°C | Anti-slip elastomeric coating |
| Potable-water reservoir lining | 6–10 | NSF/ANSI/CAN 61 / AS/NZS 4020:2018 | Residual VAM < 10 ppm | Spray-applied tank lining |
| Effluent sump lining | 8–12 | ASTM C1012/C1012M-18 / ASTM C267-20 | Expansion ≤ 0.10% at 6 months | Sulfate-resistant lining mortar |
| Coastal splash-zone repair | 4–6 | EN 1504-3:2006 / EN 1504-2:2004 | Moist cure 7 days before salt spray | Chloride-resistant repair mortar |
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Redispersible polymer powder RDP-WPC 801 is intended for dry-mix polymer-modified waterproofing coatings. The polymer base is a vinyl acetate-ethylene copolymer stabilized with a polyvinyl alcohol protective colloid and an inorganic antiblocking agent. The powder is not a cement substitute; it is a polymer modifier that re-disperses in water during mixing and coalesces into a polymer film as the cementitious layer hydrates and dries. The coalesced film interpenetrates cement hydration products, filling capillary pores and bridging microcracks that develop in cementitious coatings with a water-to-binder ratio between 0.40 and 0.50. In this function it improves crack-bridging capacity, adhesion, impermeability, and low-temperature flexibility of polymer-modified waterproofing coats.
Quality-release specifications for the as-delivered powder include non-volatile content ≥98.0 wt% determined in accordance with ISO 3251, ash residue ≤10.0 wt% by ISO 3451-1(A), bulk density 450–550 g/L by DIN EN ISO 60, and pH of a 10% aqueous dispersion in the range 6.5–8.5 by ISO 976. Glass transition temperature is −12 °C to −6 °C by differential scanning calorimetry according to ISO 11357-2:2020. Minimum film formation temperature after redispersion is ≤5 °C by ISO 2115. Residue retained on a 315 µm sieve is ≤2.0 wt% by ISO 2591-1, and residual moisture is ≤1.0 wt%. These limits are relevant to dry-mix packaging because residual moisture above 1.5 wt% produces powder blocking in warehousing above 65% relative humidity.
When the dry mix is hydrated at a water-to-powder ratio of 0.32:1 to 0.38:1 and mixed with a low-shear paddle at 300–600 rpm, the powder releases a latex-like dispersion with a mean particle diameter below 2.0 µm. The polymer particles are protected by the polyvinyl alcohol colloid against premature coagulation in the presence of calcium ions at pH up to 12.5. Film coalescence begins when capillary water is consumed by cement hydration and surface evaporation; measurable continuous film formation occurs after 72 h at 23 °C and 50% RH. On production bagging lines, bulk density variation outside 450–550 g/L causes fill-weight drift in 25 kg bags unless volumetric feeders are recalibrated.
Addition level is the primary formulation variable controlling film continuity. In a polymer-modified cementitious waterproofing mortar based on EN 197-1 CEM I 42.5 cement, a cement-to-sand ratio of 1:2.5, and a total water-to-binder ratio of 0.42, RDP-WPC 801 is normally added at 2.0–8.0 wt% of the total dry mix. At 2.0 wt%, the polymer volume is sufficient only to modify pore surfaces; elongation at break remains below 20% under ASTM D412-16, and tensile failure remains brittle. At 4.0 wt%, the polymer forms a semi-continuous film; film elongation rises to 80–150%, and pull-off adhesion to concrete reaches 1.0–1.5 MPa under ASTM D4541-17. At 6.0 wt%, the polymer film is continuous in membranes with a total wet thickness of 1.5–2.0 mm, and low-temperature crack bridging improves. Addition above 8.0 wt% creates a wet-mix viscosity increase that may require additional water; adding water raises the water-to-binder ratio and reduces compressive strength and dimensional stability.
On a 750 L horizontal ribbon blender operated at 45 rpm, a polymer dosage above 6.0 wt% can produce undispersed polymer agglomerates if the powder is added before fine fillers or if the blender fill ratio exceeds 0.70. Airless spray application of such improperly dispersed batches produces pinholes when nozzle backpressure drops below 0.35 MPa; post-filtration does not eliminate this failure mode. A defoamer addition of 0.1–0.3 wt% on total dry mix is normally required above 6.0 wt% polymer dosage because the VAE dispersion stabilizes entrained air. Wet density below 1.80 g/cm³ at 20 °C mix temperature indicates excess air that reduces water impermeability. Mixing water temperature should be controlled between 15 °C and 25 °C. Below 10 °C, the minimum film formation temperature is approached and early coalescence slows; above 30 °C, cement hydration accelerates and open time can fall below 45 min. The practical processing window of ±5 °C around 20 °C is therefore critical for continuous spray lines.
Replacement of liquid styrene-butadiene rubber latex or acrylic latex with RDP-WPC 801 changes both production logistics and membrane performance. Liquid latexes are typically supplied at 45–55% solids and require biocides, frost-free warehousing above 5 °C, and separate water metering on the jobsite. The dry VAE powder has non-volatile content ≥98.0 wt% and can be blended directly with cement, sand, and fine fillers in a one-component bag. In a standard 1:2.5 cement-sand formulation, a liquid acrylic latex at 50% solids cannot provide the same dry-mix packaging benefit; its water must be accounted for in the water-to-binder ratio. The ethylene comonomer in RDP-WPC 801 internally plasticizes the VAE chain, so no coalescing solvent is required. This differs from hard vinyl acetate homopolymer powders that require external coalescent for film formation at ≤5 °C.
The principal performance boundary occurs at low-temperature deformation. A low-Tg liquid SBR or acrylic latex with a glass transition temperature of −40 °C to −25 °C may retain elongation below −15 °C, whereas the VAE powder with Tg −12 °C to −6 °C is generally specified for cold but not severe sub-zero crack-bridging duty. When project specifications require crack bridging at −20 °C, a hybrid system with a lower-Tg styrene-acrylate powder or additional liquid polymer is required; published data for this specific configuration is limited. The dry powder allows formulations to avoid in-can preservatives and residual volatile organic compounds associated with some liquid dispersions. Compliance statements for polymer-modified cementitious waterproofing systems are typically evaluated against GB/T 23445-2009 and JC/T 984-2011.
On exterior basement and retaining-wall lines, the powder is dry-blended with ordinary portland cement, silica sand, and calcium carbonate before being mixed with water at the point of use. A low-speed paddle mixer at 300–600 rpm or a continuous screw mixer with water metering at 0.32:1 to 0.38:1 liquid-to-solid ratio is preferred; high-shear dispersion above 1,500 rpm is not required and can increase entrained air. The mixed coating is applied by brush, roller, or airless spray to a first coat thickness of 0.5–1.0 mm, followed by a second coat bringing the total wet thickness to 1.5–2.0 mm. On vertical substrates, presaturated concrete is required but free surface water must be removed; excess surface water increases the local water-to-binder ratio and reduces film coalescence. For horizontal surfaces subject to ponding water, a reinforcing glass fabric is embedded between coats. Flood testing may begin after 48 h at 23 °C, although cement hydration and polymer film maturation continue to 28 d. On high-speed bagging lines, the bulk density determines the volumetric filling target for 25 kg bags; if bulk density drifts outside 450–550 g/L, the fill volume must be adjusted to prevent underfill. A baghouse dust-collection system with a filter area sized for ≥1.0 m² per 1,000 kg/h throughput is used to control powder dust during bulk loading.
Release tests are applied to the as-purchased powder and to a standard formulation containing 4.0 wt% RDP-WPC 801 by total dry mix. Film specimens are prepared at 23 °C and 50% RH and conditioned for 28 d before mechanical testing.
| Property | Specification range | Test method |
|---|---|---|
| Non-volatile content | ≥98.0 wt% | ISO 3251 |
| Ash residue | ≤10.0 wt% | ISO 3451-1(A) |
| Bulk density | 450–550 g/L | DIN EN ISO 60 |
| pH of 10% aqueous dispersion | 6.5–8.5 | ISO 976 |
| Glass transition temperature | −12 °C to −6 °C | ISO 11357-2:2020 |
| Minimum film formation temperature | ≤5 °C | ISO 2115 |
| Sieve residue on 315 µm | ≤2.0 wt% | ISO 2591-1 |
| Film tensile strength after 28 d | 2.0–4.5 MPa | ASTM D412-16 |
| Film elongation at break after 28 d | 80–250% | ASTM D412-16 |
| Pull-off adhesion to concrete after 28 d | ≥1.0 MPa | ASTM D4541-17 |
| Film water absorption after 7 d immersion | ≤12% | ISO 62:2008 |
RDP-WPC 801 is not recommended for cement-free pure polymer films, solvent-based coatings, or systems containing amine-based accelerators that shift pH above 11.5 before film coalescence. The protective polyvinyl alcohol colloid can undergo premature destabilization under such conditions, producing grit and loss of film continuity. Contact with calcium aluminate cement systems may require additional set retarder and compatibility testing; published data for this specific configuration is limited. The powder must be stored in unopened bags at 5–35 °C and relative humidity ≤65%. In production warehouses at relative humidity above 65%, visible powder blocking has been observed within 72 h in opened or poorly sealed bags. Direct contact with water during storage must be avoided because the re-dispersed polymer will block the powder and render it unsuitable for dry-mix packaging.