| Código SH | 706893 |
| Nome Do Produto | Copolímero RDP DA-1120 VAE |
| Aparência | Pó branco de fluxo livre |
| Tipo De Polímero | Copolímero de acetato de vinilo-etileno (VAE) |
| Colóide Protetor | Álcool polivinílico (PVA) |
| Tamanho Da Partícula Resíduo De Peneira De 100 Mesh | ≤ 5% |
| Densidade Aparente | 400-600 g /L |
| Teor De Cinzas | 10-15% |
| Teor De Umidade | ≤2,0% |
| Valor De Ph Dispersão De 10 | 6,0-8,0 |
| Temperatura Mínima De Formação De Filme | 0 ° C a 5 ° C |
| Viscosidade 10 De Dispersão | 500-1500 mPa · s |
| Resistência à Adesão à Tração | Alto, adequado para sistemas à base de cimento |
| Estabilidade De Armazenamento | 12 meses em condições secas e frias |
Como fábrica certificada de Copolímero RDP DA-1120 VAE, aplicamos protocolos de qualidade rigorosos - cada lote é submetido a testes rigorosos para garantir padrões de eficácia e segurança consistentes.
| Embalagem | DA-1120 VAE Copolymer RDP é embalado em sacos de papel multicamadas de 25 kg com forro interno de polietileno, paletizado e retrátil para proteção. |
| Carga de contêiner (20' FCL) | 20 'FCL: sacos paletizados de 25 kg de DA-1120 RDP, seguro, recipiente forrado à prova d' água, protegido contra umidade e danos. |
| Envio | DA-1120 VAE Copolymer RDP é fornecido como um pó seco em sacos ou tambores à prova de umidade. Proteja da umidade e da água para evitar aglomerações; armazene em áreas frescas, secas e ventiladas. Nenhuma classificação de perigo especial, mas evite a inalação de poeira e siga os procedimentos padrão de manuseio seguro. |
| Armazenamento | Armazene o copolímero RDP DA-1120 VAE em uma área fria, seca e bem ventilada, longe da luz solar direta e fontes de calor. Mantenha a embalagem original selada intacta para evitar a absorção de umidade. Use dentro da vida útil recomendada, normalmente 12 meses, e siga a rotação do estoque pela primeira vez. Evite a exposição prolongada a condições úmidas. |
| Prazo de validade | O prazo de validade é normalmente de 12 meses a partir da fabricação, quando armazenado em condições frias e secas e mantido selado. |
Preços competitivos Copolímero RDP DA-1120 VAE que se ajustam ao seu orçamento - termos flexíveis e orçamentos personalizados para cada encomenda.
Para amostras, preços ou mais informações, entre em contato conosco em +8615380400285 Ou envie para sales2@liwei-chem.com.
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DA-1120 VAE Copolymer RDP is a spray-dried redispersible polymer powder based on a vinyl acetate–ethylene copolymer stabilized with a polyvinyl alcohol protective colloid. The grade designation DA-1120 identifies a medium-ethylene VAE composition produced for cementitious dry-mix mortar modification rather than for adhesive film casting or organic coatings. Because ethylene units are incorporated directly into the vinyl acetate chain, the polymer exhibits internal plasticization; no external coalescing solvent or phthalate plasticizer is required to lower the minimum film-forming temperature. This structural feature separates DA-1120 from polyvinyl acetate homopolymer RDP grades, which generally rely on higher residual monomer or external plasticizer levels to achieve usable film formation at 5–10 °C. The powder is supplied as a white free-flowing particulate with a bulk density in the 450–650 g/L range and a mineral anti-caking agent that maintains flow after pallet vibration and silo residence. It is intended solely as an auxiliary organic binder in hydraulically setting systems; the polymer redisperses to primary emulsion particles when mixed with water, then coalesces during drying to form discrete polymer domains that bridge capillary pores and cement grain boundaries. The product is added at dry mix dosages typically between 1.5 wt% and 6.0 wt% of total formulation. At these levels, the polymer solids modify tensile strain capacity, interfacial adhesion, and water retention, but they do not replace the cementitious binder network. Because the product is designed for dry blending, it is not recommended for post-addition to wet mortar or for use as a sole binder in coatings. In manufacturing practice, the powder is typically discharged from big bags through loss-in-weight screw feeders into a horizontal ploughshare mixer operating at 6–10 m/s tip speed; this sequence reduces segregation of the low-density polymer powder from denser silica sand and cement fractions.
Incoming inspection protocols verify batch-to-batch consistency with the following methods. The values below are representative acceptance windows for DA-1120; the manufacturer lot-specific certificate of analysis remains the controlling document for each delivery. Production sites that unload into outdoor silos should repeat bulk density and residual moisture before pneumatic transfer because storage under high relative humidity can alter both parameters.
| Property | Acceptance Window | Test Method |
|---|---|---|
| Appearance | White free-flowing powder | Visual inspection |
| Non-volatile solids | ≥ 98.0 wt% | ISO 3251 |
| Ash content | 10.0–14.0 wt% | ISO 3451-1 |
| Residual moisture | ≤ 2.0 wt% | ISO 787-2 |
| pH of 10% dispersion | 6.0–8.0 | ISO 787-9 |
| Bulk density | 450–650 g/L | ISO 697 |
| Sieve residue on 212 µm | ≤ 5.0 wt% | ISO 2591-1 |
| Minimum film-forming temperature | 0–3 °C | ISO 2115 |
| Glass transition temperature, DSC | -7 to -5 °C | ISO 11357-2 |
A bulk density drift greater than ±10% from the reference value can alter volumetric screw feeder calibration and cause binder content drift in continuous mortar lines. Bulk density below 400 g/L has been associated with under-dosing at constant feeder RPM, while material above the 212 µm residue limit is associated with delayed redispersion and visible polymer specks after trowel finishing. These defects become more frequent when the powder has been stored above 60% relative humidity, because the protective colloid bonds partially to surface moisture and forms slow-dispersing agglomerates. The incoming QC bench test should therefore include both dry sieve residue and a qualitative redispersion test in water at 20 °C under low-shear agitation; a smooth, blue-white dispersion without coarse grains indicates acceptable primary particle release.
In cementitious tile adhesive applications, the critical performance change occurs between 1.5 wt% and 3.0 wt% DA-1120 addition. Below approximately 1.0 wt%, the polymer solids are insufficient to form a continuous interpenetrating network with cement hydration products; tensile adhesion measured by EN 1348 after 28 days dry conditioning commonly remains below 0.3 MPa. Between 3.0 wt% and 5.0 wt%, the polymer film provides measurable improvements in cohesive failure mode, open time, and water resistance. Typical formulations for C1 or C2 tile adhesives under EN 12004 use 3.0–4.5 wt% DA-1120 combined with cellulose ether, calcium formate or another setting accelerator, and a Portland cement–silica sand base. The ethylene-vinyl acetate composition gives DA-1120 a glass transition in the -7 to -5 °C range; this enables film coalescence at substrate and ambient temperatures above 5 °C without the plasticizer migration problems observed in certain vinyl acetate homopolymer grades. However, the product should not be interpreted as a substitute for high-performance acrylic RDP in very low-energy glazed tile adhesion under water immersion; published data for this specific configuration is limited, and formulation-specific testing under EN 1348 water immersion is required.
Process conflicts arise when the powder is added directly into the vortex of a high-speed disperser above 1,500 rpm. The rapid wetting of the protective colloid can generate localized gel aggregates that persist after mortar mixing and appear as lumps in the trowel bed. The preferred sequence is to pre-blend DA-1120 with cellulose ether and fine sand for 90–180 seconds in a ribbon or ploughshare mixer before adding cement and water. On continuous dry-mortar lines, the powder is best introduced through a loss-in-weight feeder after the mineral fraction has reached a homogeneous state; this reduces dust losses and prevents accumulation on mixer walls. Mortar producers have reported that dust extraction systems pulling more than 0.3 m/s air velocity across the mixer can remove low-bulk-density polymer particles before they are incorporated, leading to lower-than-target polymer content in the final dry blend.
The substitution of DA-1120 VAE RDP for a PVAc homopolymer RDP generally lowers the minimum film-forming temperature and improves low-temperature flexibility without increasing volatile coalescent demand. PVAc homopolymer RDP grades typically exhibit MFFT values above 12 °C, which can limit film formation in cold-weather tile installation. DA-1120, with an MFFT of 0–3 °C, permits thin-bed work at substrate temperatures of 5–10 °C. Compared with acrylic RDP, DA-1120 usually occupies a lower cost position and delivers adequate alkali resistance in cementitious environments; however, acrylic polymers often retain better adhesion to vitrified tile and lower water absorption after immersion. The substitution is not always one-to-one. In formulations where DA-1120 replaces an acrylic RDP, the dosage may need to be increased by 0.5–1.0 wt% to maintain equivalent EN 1348 water immersion adhesion, but dry compressive strength can remain higher because of the softer VAE film. In contrast, replacing a PVAc homopolymer RDP with DA-1120 can often be done at equal dosage while increasing flexibility; the formulation should be re-tested for open time because the protective colloid and ethylene content affect water retention and skin formation.
| Comparative Parameter | DA-1120 VAE RDP | PVAc Homopolymer RDP | Acrylic RDP |
|---|---|---|---|
| Minimum film-forming temperature, ISO 2115 | 0–3 °C | 12–20 °C | -10 to 0 °C |
| Water immersion adhesion in cement tile adhesive, EN 1348 | typically 0.5–1.0 MPa at 3.0–5.0 wt% | often 0.2–0.5 MPa due to higher hydrophilicity | 0.6–1.2 MPa depending on protective colloid and dosage |
| Adhesion to vitrified tile after heat ageing, EN 1348 | moderate to high; formulation-dependent | lower; brittle at high polymer content | high; controlled by base acrylic chemistry |
| Alkali resistance | high; ethylene-vinyl acetate backbone stable in cement pore solution | high, but film is stiffer | high; some anionic grades may be sensitive to calcium ions |
| Relative formulation cost position | reference | lower in some markets | higher |
These comparisons are class-level and are not a substitute for formulation-specific testing. For DA-1120, published data for certain high-temperature or fully exterior UV-exposed applications is limited; the product is therefore specified primarily for cementitious base coats, tile adhesives, self-leveling compounds, and repair mortars where the organic phase is protected from direct solar exposure by mineral overlays.
DA-1120 is compounded with calcium aluminate, anhydrite, and Portland cement in self-leveling underlayments at addition levels of 2.0–6.0 wt%. The polymer modifies plastic viscosity and surface film formation while helping to control dusting. At dosages above 6.0 wt%, early compressive strength can decline by 10–20% at 24 hours relative to an unmodified control, because the polymer film coats cement grains and retards hydration. This threshold is critical in commercial underlayment work where foot traffic or covering is scheduled within 24–48 hours. Ring flow measured by EN 12706 can typically be maintained at 145–155 mm with 5–10% less water when DA-1120 is present at 3.0 wt%; water reduction must be confirmed with the specific water-reducing agent and plasticizer system because incompatible plasticizers can increase air entrainment. The powder is also used in repair mortars at 2.0–8.0 wt%, where tensile crack-bridging and low shrinkage are required. Published data for high-build vertical repair mortars with DA-1120 above 8.0 wt% is limited; higher dosage may require rheology adjustment with water-retaining agents and should not be extrapolated from standard tile adhesive tests.
Unopened bags should be stored in covered, dry conditions at 5–35 °C. Relative humidity above 60% accelerates surface moisture uptake, which leads to lump formation and slow redispersion. Under high-humidity storage, bags should be re-screened through a 500 µm sieve before addition to dry-mix lines. The powder is not classified as flammable; however, the organic content can form combustible dust clouds if airborne concentrations exceed the lower explosive limit. Pneumatic conveying with un-dried compressed air is not recommended because condensation at the conveying line wall can hydrate the protective colloid and deposit material. Incompatibility is observed with dry blends containing high concentrations of free calcium oxide; local exothermic hydration can raise temperature above 80 °C and degrade the polyvinyl alcohol colloid, reducing redispersibility. The product should not be exposed to steam cleaning, open water sprays, or outdoor uncovered storage. Typical shelf life in original packaging is 6–12 months from the date of manufacture; material older than 12 months may require QC revalidation for residual moisture, bulk density, and redispersibility before use. Production sites in humid coastal regions often specify moisture barrier liners and limit open bag standing time to less than 8 hours to avoid pre-hydration of the powder in the weighing area.