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Anhui Liwei Chemical Co., Limited.

DA-1122 VAE Copolymer RDP

    • Product Name: DA-1122 VAE Copolymer RDP
    • 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 105499
    Product Name DA-1122 VAE Copolymer RDP
    Chemical Composition Vinyl Acetate-Ethylene copolymer
    Appearance White or off-white free-flowing powder
    Redispersibility Excellent; forms a stable emulsion when mixed with water
    Solid Content 99-100%
    Ash Content ≤ 1%
    Bulk Density 400-600 g/L
    Particle Size 98% passing through 250 μm sieve
    Ph 10 Percent Dispersion 6.0-8.0
    Minimum Film Forming Temperature 0-5°C
    Glass Transition Temperature 0-10°C
    Water Resistance Good after film formation
    Adhesion Strength High, suitable for cementitious and gypsum systems

    As an accredited DA-1122 VAE Copolymer RDP factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing DA-1122 VAE Copolymer RDP is supplied in 25 kg multi-layer paper bags with moisture-proof lining, ensuring safe handling and storage.
    Container Loading (20′ FCL) DA-1122 VAE Copolymer RDP is loaded as a full 20-foot container load, palletized, protected from moisture, and secured for safe transport.
    Shipping DA-1122 VAE Copolymer RDP ships as a free-flowing white powder in moisture-proof laminated bags or drums. Keep dry, sealed, and away from direct sunlight during transit. Avoid dust accumulation and ignition sources. Handle with adequate ventilation; use protective gloves and eyewear. Standard non-hazardous chemical shipping applies.
    Storage Store DA-1122 VAE Copolymer RDP in a cool, dry, well-ventilated area, away from direct sunlight and heat sources. Keep the original packaging sealed to prevent moisture absorption, as humidity causes caking and performance loss. Recommended storage temperature below 30°C. Unopened, use within six months; once opened, reseal tightly and consume promptly.
    Shelf Life Store in a cool, dry place. Shelf life is typically 12 months from date of manufacture when unopened.
    Application of DA-1122 VAE Copolymer RDP

    In cementitious ceramic tile adhesives, DA-1122 is dry-blended at 1.5–3.0% by total batch weight when the target classification is C2TE under ISO 13007-1:2010. The powder is not pre-hydrated at the manufacturing plant; it is introduced into a horizontal double-ribbon mixer with variable-frequency drive at 18–24 rpm, followed by a total mixing cycle of 6–10 min. Batch temperature is kept below 35°C because hot freshly ground cement causes partial coalescence of the redispersible polymer particles and lowers free-flow stability. The finished dry mix is packed in moisture-barrier paper bags with residual moisture held below 0.3% by Karl Fischer titration. On production-scale trials, a 500 L ribbon mixer charged at 80% usable capacity produced bulk density variation of ±2.5% when DA-1122 was added at the start of the cycle; late addition after the filler pre-blend reduced that variation to ±0.8%.

    The primary performance requirement is tensile adhesion on concrete after defined conditioning cycles. At 2.0% dosage, the initial dry tensile adhesion target is ≥1.0 N/mm² for a C2-classified adhesive; water immersion specimens must also retain ≥1.0 N/mm² under the ISO 13007-2:2010 conditioning sequence. Open time measured after 30 min on a low-suction stoneware tile must be ≥0.5 N/mm² for the E option. Slip is evaluated with a 60×60 cm porcelain tile on a vertical wall; the T option requires vertical displacement ≤0.5 mm. Mixing at the job site uses a dual-shaft high-torque paddle mixer at 600–800 rpm for 3–4 min; induction times shorter than 5 min do not permit complete redispersion and lead to trapped air pockets that reduce tensile values by 0.2–0.3 N/mm² in field pull-off tests. Calcium formate accelerator at 0.5–1.0% of dry mix is compatible, while amine-based accelerators above 0.2% may destabilize the VAE film during wet storage and require trial blending before production. Terminal products include large-format porcelain panels ≥900×900 mm, stone tiles over underfloor heating, and installations on gypsum overlay boards in wet-service perimeter zones.

    What Restricts Slump Flow Stability at Water-to-Powder Ratios Above 0.24 in Self-Leveling Compounds?

    The primary process conflict in high-flow cementitious underlayments is not initial flow but segregation of the binder phase at water-to-powder ratios above 0.24. DA-1122 is incorporated at 2.0–4.5% by total dry weight in a continuous planetary mixer with 150 kg/min output; its polymer film contributes to fines retention after the high-range polycarboxylate ether superplasticizer has induced fluidity. The system is tested by a 35 mm internal diameter and 60 mm height ring. Flow spread after 5 min is specified at 130–150 mm; values below 120 mm after 30 min indicate overdosage of the polymer or excessive early aluminate hydration. In one production trial, addition of DA-1122 before pre-dispersed fillers increased between-batch flow variation from ±4 mm to ±9 mm, requiring a shift to post-filler introduction with the mixer maintained at 35–45 rpm.

    Mechanical requirements under EN 13813:2002 for a CT-C25-F5 screed are ≥25 N/mm² compressive strength at 28 d and ≥5 N/mm² flexural strength per EN 13892-2:2002. At 3.0% DA-1122, drying shrinkage is controlled below 0.5 mm/m when the applied layer is cured with polyethylene film for 48 h; thickness ranges from 3 mm feather-edge to 15 mm full pour. The finished surface is intended for vinyl, LVT, or direct polished concrete after shot blasting. Terminal products include hydronic heating underlayments over PEX or aluminium diffusion plates, renovation screeds over old concrete slabs with bond promoter priming, and industrial toppings in warehouses with rolling-load traffic.

    External Thermal Insulation Composite Base Coats and Impact-Resistant Mesh Embedment

    External thermal insulation composite base coats use DA-1122 at 2.5–4.0% by total dry mortar weight. The dry compound is mixed with 20–22% water in a forced-action paddle mixer at 400–600 rpm for 3–5 min. The wet base coat is applied by steel trowel at 3–5 mm, and an alkali-resistant glass fiber mesh with 145–165 g/m² is embedded with 2–3 mm cover. At dosages below 2.0%, the mesh becomes visible after final troweling, and hard-body impact at 3 J under EAD 040083-00-0404 produces crack propagation from the mesh plane. Above 5.0%, skin formation is retarded at 5°C and 75% RH, and the vertical base coat sags before the surface is sufficiently set for finish application. In production-scale façade lines using a notched trowel machine at 8 m/min, the failure mode at high dosage was surface drag and fiber pull-out rather than cohesive substrate failure. The base compound therefore sits within a narrow working window that must be revalidated when bulk cement fineness exceeds 4,500 cm²/g by Blaine method.

    PropertyStandardConditionRequirement
    Bond strength to EPSEN 13494:2002Dry conditioning≥0.08 N/mm²
    Bond strength to EPSEN 13494:2002Water soak≥0.03 N/mm²
    Hard-body impactEAD 040083-00-04043 JNo crack
    Water vapour diffusionEN ISO 7783:2018Wet-cup≤2.0 m Sd

    Pull-off adhesion to expanded polystyrene board is tested by EN 13494; dry-conditioned values above 0.08 N/mm² and water-soaked values above 0.03 N/mm² are used as acceptance criteria. The finish coat is applied only after the base coat has cured for 24–48 h at 10–25°C. At 3.0% polymer content, the water vapour diffusion-equivalent air layer thickness determined by EN ISO 7783:2018 remains below 2.0 m, which is required to avoid interstitial condensation in cold-climate assemblies. Terminal products include expanded polystyrene boards on concrete block façades, mineral wool dual-density boards in rainscreen subbase applications, and window reveal reinforcement where stress concentration around openings exceeds the unreinforced coating capacity.

    Hydrophobic Film Formation Limits Water Vapour Transmission in One-Component Slurry Waterproofing

    One-component cementitious waterproofing slurries are compounded with DA-1122 at 2.0–3.5% by total dry weight. The powder is dry-blended into the mortar, then mixed on site with 0.28–0.32 water-to-powder ratio and applied by stiff brush in two layers. Total dry film thickness is held at 1.0–1.5 mm; a single layer above 2.0 mm develops early surface skin and entraps water that later blisters under water immersion. Water impermeability is tested to EN 14891:2017 on a 20 mm concrete slab at 1.5 bar for 7 d; penetration through the coating must remain at 0 mm. Crack bridging is evaluated at −5°C, with a pass value of ≥0.75 mm for flexible cementitious slurries. When DA-1122 is reduced below 2.0%, low-temperature crack bridging drops to 0.3–0.5 mm and the coating fails by brittle crack propagation at the concrete surface.

    The cured membrane must maintain water vapour permeability sufficient to prevent osmotic delamination of tiles when a balcony deck is saturated from behind; the vapour diffusion equivalent air layer thickness tested by EN ISO 7783:2018 should remain between 0.5 m and 2.0 m. The terminal parts include balcony waterproofing beneath porcelain tiles, wet-room tanking under stone or mosaic, and internal tanking of service water structures where the 1.5 mm film is cured for 48 h before immersion.

    For structural repair mortars specified under EN 1504-3:2005 class R4, DA-1122 is incorporated at 2.0–4.0% in formulations with a 0.35–0.40 water-to-cement ratio. The polymer does not replace shrinkage compensation but modifies the fracture mode of the repair layer. High-shear mixing with a dispersion ring at 900–1200 rpm is required because low-shear paddle mixers fail to redisperse the powder uniformly in high-strength grouts with silica fume or metakaolin. At 4.0% dosage, compressive strength at 28 d may decrease by 8–12% relative to the unmodified control, while flexural strength tested by EN 1015-11:2019 increases. Water vapour permeability under EN ISO 7783:2018 should remain between 0.5 m and 2.0 m equivalent air layer thickness to avoid trapping moisture behind the patch. Pre-drying of the substrate is required at relative humidity above 60%; otherwise the wet film remains soft at the interface and pull-off adhesion under EN 1542:1999 falls below 0.8 N/mm² for traffic-bearing repairs. Patch thickness above 40 mm requires separate shrinkage compensation and published data for this specific configuration is limited. Terminal products include bridge deck spall repairs, car park ramp patching, and grout bedding of steel baseplates.

    When Gypsum Substrates Require Film Flexibility Without Inducing Premature Set Retardation

    A dosage of 1.0–2.5% by total dry batch weight is used in gypsum-based joint fillers and patching compounds. Setting time is verified with a Vicat apparatus under ASTM C474-15; the final set should remain at or below 90 min at 23°C and 50% RH. DA-1122 is added in the dry phase after stearate-coated fillers because direct addition to humid plaster can initiate partial agglomeration. The resulting joint compound must have thin-film crack resistance sufficient for 2 mm embedded paper tape over recessed joints; the paste is applied in two coats with a 150 mm broad knife, with the second coat thinned to a 0.5 mm feathered edge. Terminal products include paper-faced gypsum board jointing, patching of gypsum block before paint, and skim coating over gypsum plaster with high suction backgrounds.

    Pigmented through-body finishes over high-suction backgrounds require DA-1122 at 1.5–2.5% by total dry weight. The finish mortar is spray-applied with a hopper gun at 2–4 bar air pressure and trowelled to 2–3 mm thickness. Capillary water absorption coefficient is tested by EN 1015-18:2002; the target is ≤0.2 kg/(m²·min0.5) for W2-classified render. Adhesion tested by EN 1015-12:2016 should remain above 0.25 N/mm² after 7 d; above 3.0%, the surface becomes tacky before final troweling and adhesion drops below that threshold. Terminal products include decorative façade renders on expanded clay block, interior skim coats over patched concrete, and tinted base layers under silicate final coats.

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    Certification & Compliance
    More Introduction

    Model DA-1122 VAE Copolymer RDP is supplied as a free-flowing white powder manufactured by spray drying a vinyl acetate–ethylene copolymer dispersion onto a protective colloid and anti-caking matrix. The product is intended for dry-mix cementitious and gypsum-based formulations in which water added during application must re-disperse the polymer into a stable aqueous dispersion that coalesces during drying and forms a continuous polymer film within the mineral matrix. Published product-specific datasheets for DA-1122 are limited; therefore the following specification envelope reflects the typical industrial release window for commercial vinyl acetate–ethylene redispersible polymer powders with comparable ethylene content and polyvinyl alcohol stabilization. Exact batch values should be confirmed against the manufacturer’s certificate of analysis.

    The physical and thermal values below define the usual quality window for a mid-range VAE RDP of this class.

    PropertyTypical industrial rangeReference method
    Appearancewhite free-flowing powdervisual
    Solids content≥98 %ISO 1625
    Ash content at 1000 °C10–14 %ISO 3451-1
    Bulk density450–650 g/LDIN EN ISO 60
    Residual moisture≤2.0 %ISO 760
    pH of 10 % dispersion6.0–8.5ISO 976
    Minimum film-forming temperature0–5 °CISO 2115
    Residue on 315 µm sieve≤2 %ISO 4610
    Glass transition temperature−7 to +5 °CISO 11357-2

    Why does DA-1122 differ from conventional VAE RDP grades in cementitious binding performance?

    The primary differentiation of DA-1122 is its vinyl acetate–ethylene monomer distribution and the resulting balance among film flexibility, water resistance, and alkali resistance. In conventional polyvinyl acetate homopolymer or low-ethylene VAE powders, the acetate ester groups are susceptible to alkaline hydrolysis in cement pore solutions with pH above 12.5. That hydrolysis converts surface polymer chains to polyvinyl alcohol, increasing hydrophilic character and reducing wet tensile adhesion after water immersion. DA-1122’s ethylene comonomer content increases steric shielding of the acetate ester groups and lowers the saponification rate under high-pH conditions encountered during portland cement hydration. In practice, this is observed as higher residual adhesion after 21-day or 28-day water immersion in cementitious tile adhesive formulations evaluated according to EN 12004-1:2017 and ISO 13007-1.

    Unlike VAE powders that require external phthalate plasticizers for low-temperature flexibility, DA-1122 achieves film elongation through the ethylene sequence distribution. Migration kinetics of plasticizing additives therefore do not govern long-term embrittlement in this grade, because no external liquid plasticizer is present. Compared with acrylic RDP grades, DA-1122 tends to exhibit lower water demand in high-filler formulations and better compatibility with polyvinyl alcohol-stabilized rheology modifiers. Acrylic powders may offer higher ultraviolet resistance and greater hydrophobicity in exposed thin-film applications, but VAE grades generally provide more reliable wet adhesion to cementitious substrates at comparable dosage. Published comparative data for DA-1122 specifically remain limited; differences depend on cement type, filler surface area, water-to-binder ratio, and addition rate.

    Typical addition levels range from 1.5 % to 4.0 % of total dry mix for C1 and C2 tile adhesives. At the lower end, the polymer improves workability and wet adhesion without excessive retardation. At the upper end, flexibility and open time increase, but 28-day compressive strength measured by ASTM C109/C109M may decline because the polymer phase is less stiff than cement hydrates. The exact reduction is formulation-dependent and cannot be transferred from one cement source to another without verification.

    During production-scale dry-mix manufacturing, DA-1122 is introduced at the start of the dry-blend sequence after the mineral binder and before fine fillers. In a 1000–2000 kg single-shaft ploughshare mixer with a tip speed of 8–15 m/s, dispersion is typically adequate within 120–180 s; longer mixing does not improve homogeneity and may raise bulk powder temperature through friction. In low-shear horizontal paddle mixers of 500–1500 kg capacity operating at 60–80 rpm, batch cycle times of 3–5 min are common. The powder is thermoplastic, and the bulk powder temperature should remain below 45 °C to prevent particle sintering, wall buildup, and screen blinding. Field experience indicates that screw conveyors with tight clearances can generate frictional heat at transfer points, causing partial film formation and blocking of 500 µm sack-off sieves. Maintaining residual moisture below 2.0 % and storing the powder in sealed silos at relative humidity below 60 % reduces caking. If exposure to humid air occurs, pre-drying is not generally recommended because fluidized-bed temperatures above 40 °C may fuse the polymer particles. Instead, transfer to a climate-controlled hopper and sieve through 500 µm before dosing.

    Gravimetric dosing with load-cell tolerance of ±0.5 % is preferred over volumetric screw dosing because bulk density can vary between 450 g/L and 650 g/L. Calibration with the actual production blend is necessary when fillers of different particle morphology are used, because differences in electrostatic charge and flowability can shift the screw fill factor. For dry-mix tile adhesives, DA-1122 is typically combined with cellulose ether, calcium formate accelerator, and air-entraining or defoaming agents. For high-performance C2 formulations, the polymer is not the sole source of wet adhesion; cement selection, water dosage, and curing regime remain critical variables.

    Polymer film coalescence and water resistance in high-pH matrices

    In alkaline cementitious matrices with pore-water pH above 12.5, film formation occurs after the hydrating cement consumes sufficient water to allow polymer particles to pack and interdiffuse. The minimum film-forming temperature of 0–5 °C permits coalescence at substrate temperatures as low as 5 °C. Below that boundary, film formation remains discontinuous and adhesion development is retarded. After coalescence, the polymer film is no longer re-dispersible in water, although the dry powder redisperses readily before setting if the dry mix is re-wetted. Water immersion tests on C2 tile adhesives can reveal whether the polymer phase is effectively bridging microcracks at the tile–mortar interface. Adhesion after water immersion for 21 days at 23 °C is typically required to be ≥1.0 MPa under EN 12004-1:2017. For C2S1 or C2S2 classified adhesives, transverse deformation values of ≥2.5 mm or ≥5.0 mm under EN 12002 are relevant. In high-pH patch repair mortars, DA-1122 can reduce surface cracking, but the polymer cannot compensate for shrinkage when the water-to-binder ratio exceeds the stability boundary of the formulation.

    The alkaline hydrolysis of vinyl acetate is a pseudo-first-order process with respect to hydroxyl ion concentration. Ethylene units reduce the frequency of ester hydrolysis by limiting water access at the polymer backbone. This effect allows DA-1122 to retain film integrity longer than a low-ethylene VAE powder in wet alkaline environments. However, prolonged contact with saturated calcium hydroxide solution at elevated temperature can still degrade the polymer phase. Therefore DA-1122 is not recommended as the sole binder in continuously immersed structural repair applications unless long-term adhesion is validated by testing according to the relevant national or European product standard for the intended exposure class.

    When DA-1122 is used in self-leveling underlayments and repair mortars

    Formulations incorporating DA-1122 in self-leveling underlayments require a balance between flow retention, polymer segregation resistance, and surface hardness. Typical addition rates are 1.0–3.0 wt% of total dry mix in calcium sulfoaluminate-modified portland cement systems. Flow diameter is measured by the ring method according to EN 12706; flow values of 130–150 mm after mixing are frequently targeted, but published data for this specific configuration are limited. In repair mortars, addition levels of 2.0–5.0 wt% improve adhesion to prepared concrete substrates and reduce permeability. The powder is not a substitute for proper surface preparation; concrete substrates should have a minimum tensile bond strength of 1.5 MPa and be free of laitance, curing compounds, oil, and loose particles.

    DA-1122 can be combined with cellulose ethers, polycarboxylate ether superplasticizers, and calcium formate accelerators. Amine-based accelerators should be avoided because they may destabilize the re-dispersed polymer dispersion and produce local gelation. Pot life of the mixed mortar should be monitored because re-dispersed VAE polymers can increase viscosity retention and reduce water demand, but over-mixing at high shear can entrain air and lower hardened density. In cementitious grouts and external thermal insulation composite system base coats, addition rates of 2–4 wt% are generally sufficient to improve workability and crack resistance. The powder is not intended for use in solvent-borne systems, and ultraviolet exposure in exterior topcoats should be addressed with a mineral or opaque protective layer rather than relying on the VAE polymer alone.