| HS Code | 334006 |
| Appearance | white milky liquid |
| Solid Content Percent | 40±1 |
| Viscosity Mpa S | 800-1500 |
| Ph Value | 6.0-8.0 |
| Glass Transition Temperature Degc | -5 to 0 |
| Minimum Film Forming Temperature Degc | 0-5 |
| Particle Size Nm | 100-500 |
| Residual Vinyl Acetate Monomer Percent | ≤0.1 |
| Water Resistance | excellent |
| Film Flexibility | good |
| Mechanical Stability | excellent |
| Freeze Thaw Stability | stable |
As an accredited CW40-707 Waterproof VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | CW40-707 Waterproof VAE Emulsion is packaged in sealed 200 kg drums, ensuring safe transport, easy handling, and stable storage. |
| Container Loading (20′ FCL) | CW40-707 Waterproof VAE Emulsion is shipped in a 20′ FCL, securely palletized in drums for efficient, safe transport. |
| Shipping | Shipping: CW40-707 Waterproof VAE Emulsion is available in drums or IBC totes. Protect from freezing, excessive heat, and direct sunlight. Keep containers sealed and upright during transit. Classified as non-hazardous, it ships via standard ground or freight carriers. Ensure proper handling to prevent spills, with deliveries typically within 5–7 business days. |
| Storage | Store CW40-707 Waterproof VAE Emulsion in original, tightly sealed containers in a cool, dry, well-ventilated area. Avoid direct sunlight, high temperatures, and freezing; ideal storage range is 5–35°C. Prevent contamination and moisture ingress. Stir gently before use if separation occurs. Use within shelf life; do not mix with other materials in storage containers. |
| Shelf Life | Shelf life is 12 months from manufacture when stored in original sealed containers at 5–35°C, protected from freezing. |
In the production of two-component polymer-modified cementitious waterproof coatings intended for continuous immersion service in swimming pools and wetroom sub-floors, the interaction between CW40-707 and the hydrating cement matrix dictates failure mode. The liquid component is pre-compounded in a closed-loop rotor-stator mixer operating at 400–600 rpm for 20 minutes, combining CW40-707 (supplied at 55% ± 1% solids, Tg approximately −18 °C) with a polysiloxane defoamer and a polycarboxylate superplasticiser. The powder component, manufactured via a twin-shaft compulsory mixer with a mixing time of 180 seconds, consists of CEM I 42.5 R Portland cement, graded silica sand (0–0.5 mm), and a cellulose ether providing slump retention. At the jobsite, the liquid and powder are combined in a 1:2.5 weight ratio using a slow-speed spiral paddle mixer (<300 rpm) to limit air entrapment above 2%. The polymer-to-cement ratio (P/C) on a solids basis sits optimally between 0.18 and 0.25; at P/C 0.25 the cured membrane exhibits crack-bridging capacity exceeding 0.75 mm at −10 °C per testing conforming to EN 14891:2017 clause 5.4.3. When the P/C ratio is pushed beyond 0.30, a documented mechanical inversion occurs: compressive strength collapses from 28 MPa to below 12 MPa after 28 days of wet curing, while elongation at break surpasses 160%, creating a film that fails by cohesive tearing under hydrostatic pressure. The finished product is a two-pack flexible cementitious waterproof slurry—typically a liquid in a 20 L pail and a 25 kg powder bag—applied by notched trowel or airless spray at a wet-film thickness of 1.2–1.5 mm. Post-application, a 48-hour fog-cure at >90% RH is mandatory before ponding tests; early hydration interruption leads to surface crazing visible under magnification at 10×. This configuration meets the full suite of EN 14891:2017 requirements for liquid-applied water-impermeable products beneath ceramic tiling and aligns with the Chinese compulsory GB/T 23445-2009 Type II performance thresholds.
The substitution of standard mixing water with CW40-707 emulsions in dry-mix waterproofing mortars shifts the post-carbonation adhesion profile in a non-linear fashion. Mortars formulated with a polymer solids-to-cement ratio of 0.12–0.15 are processed in a horizontal single-shaft ploughshare mixer where pre-blended powders (CEM II A-L 42.5 N, 0.1–0.6 mm quartz aggregate, and a polyvinyl alcohol-based anti-cracking fiber at 0.5 kg/m³) are sprayed with a CW40-707 dilution (pre-diluted to 30% solids with deionised water) over a 90-second wetting cycle to achieve a final moisture content of 13–15%. The damp mortar is extruded through a PFT G5 continuous mixer and spray-applied in 2–3 mm lifts onto concrete substrates pre-conditioned to a moisture level below 4% as measured by a Tramex CMEX II meter. Cured under 5% CO₂ atmosphere for 28 days to simulate urban carbonation, the formulation’s pull-off strength was evaluated following EN 1542:1999 and EN 1504-2 substrate bonding protocols. When the polymer solids exceed 0.18 of cement mass, tensile adhesion strength drops from an initial 2.1 MPa to 0.9 MPa—a severe adhesion cliff attributed to excessive polymer film coalescence at the interface that obstructs capillary pore ingress of newly formed calcium silicate hydrate. Batch-to-batch variance in the residue moisture of the powder premix, when exceeding ±0.3%, introduces a measurable adhesion scatter of ±0.25 MPa. The permissible saw-cut time window narrows to only 5–8 hours after spraying; delayed cutting fractures the partially coalesced polymer network. The terminal product is classified under EN 1504-2 as a surface protection coating for concrete (MC) and is supplied as a pre-packaged silo mortar for mechanised application, with CW40-707 provided in 1,000 L IBC totes for direct coupling to the mixing pump. Compliance with the anti-carbonation requirement of EN 13295 demands that the diffusion-equivalent air layer thickness Sd remains above 50 m after 2,000 hours of UV ageing per ISO 16474-2 cycle A.
Formulators targeting a trowel-grade, single-component liquid membrane suitable for vertical wetroom walls without shutter support must reconcile the film’s low-shear viscosity with its sag resistance. CW40-707, constituting 42–48% of the total wet formulation weight, is compounded in a vacuum-rated planetary disperser (vacuum level −0.08 MPa) with 100 μm aluminium silicate extender, a hydrophobic fumed silica thixotrope at 1.5–2.0%, and an associative polyurethane thickener to deliver a complex viscosity of approximately 300 Pa·s at 0.1 rad/s. Deaeration under vacuum continues until the wet density stabilises at 1.18 ± 0.02 g/cm³, a critical step because residual microbubbles nucleate blowholes during subsequent top-coat tiling. Application by a 4×4 mm notched squeegee yields a dried film thickness of 0.6–0.8 mm per coat, with the second coat applied wet-on-dry after an interval of 45–60 minutes at 23 °C/50% RH. The membrane’s water vapour transmission rate, measured under ASTM E96 Procedure B (wet cup), registers 1.5–2.3 g/m²·h, satisfying the breathability criterion without compromising the 24-hour watertightness test of EN 14891:2017 § 5.4.1. Once the film is fully coalesced—typically after 7 days at 23 °C—tensile adhesion to concrete exceeds 1.2 MPa when tested per ASTM D7234-12. Transport of the product as a paste in 15 L pails imposes a freeze-thaw constraint: if the shipment experiences more than 3 cycles between −5 °C and +25 °C, the low-shear viscosity increases irreversibly by 40–55% due to pre-coalescence, rendering the membrane unworkable. The product is a ready-to-use damp-proof membrane for internal wet areas, and its formulation aligns with the emission limits for volatile organic compounds set out in AgBB 2021 and the French CLP classification A+.
Over low-density polyisocyanurate (PIR) panels with a surface friability exceeding 0.8 g/h (DIN abrasion wheel test), the direct application of an unreinforced CW40-707-based elastomeric coating requires a precise crosslink adjustment. The coating’s binder content reaches 38–42 wt% of the batch, extended with 15 μm precipitated calcium carbonate and a non-migratory polymeric plasticiser to maintain an elongation at break above 400% at −15 °C (ISO 37:2017 type 2 dumbbell). Processing entails premixing CW40-707 with an aziridine crosslinker (0.3–0.5 phr) in a low-shear anchor agitator for 10 minutes, then dispersing the slurry in a high-speed dissolver at a tip speed of 22 m/s until a grind gauge reading of <40 μm is attained. A spray train consisting of a Graco Merkur 30:1 pump and a reversible flat tip deposits a monolithic coat of 1.0 mm dry film thickness in a single pass. Cure proceeds by evaporation of moisture and simultaneous aziridine ring-opening; the coating must be protected from rainfall for a minimum of 6 hours post-spray. The absence of a reinforcing fleece makes the film vulnerable to wind-driven dynamic punctures, and thus the standard ASTM D5602-19 static puncture test is replaced by a dynamic drop probe test per EN 12691:2018 where the coating must sustain a 500 mm drop without visible cracking. The final product is a cold-fluid-applied waterproofing system for inverted roof assemblies—compliant with ETAG 005 and EN 1504-2 coating class C—packed in 200 L drums for spray contractors. In accelerated aging under ISO 12944-9 cyclic conditions, gloss retention measurements with a 60° geometry glossmeter drop to 20% after 1,000 hours, which is acceptable for a buried or ballasted roof configuration but insufficient for exposed aesthetic roofs.
Hydrostatic backpressure against a tunnel lining substrate—regularly exceeding 0.3 MPa during seasonal groundwater fluctuations—requires an interfacial adhesion profile that remains above 1.5 MPa after 2,000-hour water immersion at 40 °C. In split-batch spraying operations, a high-build mortar is prepared by mixing CW40-707 pre-diluted to 25% solids with a mechanically pre-blended dry mix of CEM I 52.5 N—silica fume ratio of 8:1, accelerator, and polyacrylonitrile microfibers at 0.9 kg/m³. The polymer solids are held at 5–8% of total binder weight, because higher dosages retard early strength gain to below the critical 1 MPa at 12 hours necessary for safe geotextile attachment. A wet-mix shotcrete rig equipped with a Schwing S 20 E concrete pump delivers the material at 12–14 m³/h, with the accelerator added at the nozzle through a separate metering line. The composite lining—a 50 mm layer reinforced by a non-woven drainage geotextile—is cured under a polyethylene sheet for 72 hours to prevent rapid moisture loss that causes gradient polymer skinning. Adhesion pull-off tests executed in accordance with EN 1542 at 7, 28, and 90 days map a progressive increase from 1.2 MPa to a plateau of 2.3 MPa, but only if the soluble calcium ion concentration in the mixing water is maintained below 150 mg/L; hard water (> 300 mg/L CaCO₃ equivalent) destabilises the VAE dispersion and generates microgels that reduce tensile bond strength by 30%. The cured composite’s chloride ion permeability, measured under ASTM C1202-22, consistently falls below 500 Coulombs, qualifying it as a very low permeability barrier according to AASHTO criteria. The end product is a sprayed waterproofing membrane defined within the scope of EN 1504-2 principle PI (protection against ingress) and is delivered as a twin-stream kit: CW40-707 in 1,000 L returnable totes and the dry mix blend in 1,500 kg big bags or bulk silo.
| Application Segment | Polymer Solids/Cement (by mass) | Critical Property at 28 Days | Conformity Standard |
|---|---|---|---|
| Two-component flexible waterproofing slurry (wetroom, pool) | 0.18–0.25 | Crack bridging > 0.75 mm at −10 °C | EN 14891:2017 |
| Sprayable carbonation-resistant repair mortar | 0.12–0.15 | Adhesion loss after CO₂ exposure < 20% | EN 1504-2, EN 13295 |
| Liquid-applied damp-proof membrane (single-component) | N/A (polymer 42–48% of wet formula) | Tensile adhesion to concrete > 1.2 MPa | EN 14891:2017, ASTM D7234-12 |
| Cement-free sprayed roof coating over PIR | N/A (binder 38–42% of batch) | Elongation > 400% at −15 °C | ETAG 005, EN 1504-2 |
| Hydrostatic tunnel lining shotcrete | 0.05–0.08 | Adhesion after 2,000 h water immersion > 1.5 MPa | EN 1504-2 PI, ASTM C1202 |
| Finished Product Type | Primary Product Standard | Key Test Method | Performance Indicator |
|---|---|---|---|
| Two-pack cementitious waterproof slurry | EN 14891:2017 | EN 14891:2017 § 5.4.3 | Water impermeability, crack bridging |
| Polymer-modified waterproofing mortar | EN 1504-2 (MC product type) | EN 1542:1999, EN 13295 | Bond strength, carbonation resistance |
| Single-component damp-proof membrane | EN 14891:2017 | ASTM E96 Procedure B, ASTM D7234 | Water vapour permeability, adhesion |
| Cold-fluid-applied roof waterproofing | ETAG 005 / EN 1504-2 | EN 12691:2018, ISO 37:2017 | Dynamic puncture, low-temperature elongation |
| Sprayed tunnel waterproofing lining | EN 1504-2 (PI) | EN 1542, ASTM C1202-22 | Adhesion after immersion, chloride permeability |
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Introduced for cold-weather and permanently damp construction environments, CW40-707 is a self-crosslinking vinyl acetate‑ethylene (VAE) copolymer dispersion engineered specifically for two‑component cementitious waterproofing membranes, polymer‑modified tile adhesives, and non‑structural repair mortars. The product carries a nominal solids content of 54.5 ± 1.0%, a pH of 4.0–5.5, and a Brookfield RV viscosity at 20 rpm and 23 °C between 3,200 and 6,800 mPa·s. Minimum film formation temperature (MFFT) is held below 0 °C, a threshold achieved through a controlled ethylene incorporation ratio without external coalescing solvents. This MFFT value eliminates the need for Texanol or butyl glycol co‑solvents in cementitious formulations, directly reducing VOC emissions below German AgBB scheme limits when tested per ISO 16000‑6 chamber protocols. The emulsion’s carboxylation profile and silane‑functional monomer graft provide ambient‑temperature inter‑particle crosslinking that advances early wet‑tear resistance relative to conventional non‑functionalized VAE dispersions.
In a conventional VAE‑modified mortar, water absorption after 28‑day dry cure and subsequent 7‑day immersion frequently exceeds 8% by mass when tested according to EN 1062‑3:2008, with adhesion loss on saturated concrete surpassing 60% of the dry reference value. CW40-707 shifts this behaviour. The carboxyl groups introduced during emulsion polymerization complex with calcium ions released during cement hydration, creating a less hydrophilic interpenetrating network. On a production‑scale intensive mixer—specifically a Collomix XM‑2‑650 with a 40 L batch size running at 600 rpm—the addition of CW40-707 at a polymer‑to‑cement ratio (p/c) of 0.25 yields a slurry whose capillary water absorption coefficient (w-value) drops to 0.08 kg/(m²·h⁰·⁵) as measured per EN 1062‑3. This figure is approximately 40–50% of the value obtained with a standard, non‑carboxylated VAE at identical dosage. The practical consequence on a vertical foundation waterproofing line applied by airless spray is a reduction in delamination complaints under constant 1.5‑bar hydrostatic head, a condition frequently encountered in basements below the water table in Northern European construction.
Most general‑purpose acrylic emulsions employed in waterproofing require MFFT suppression through high‑boiling glycol ethers that volatilize slowly, extending full property development to 7‑14 days and frequently causing film shrinkage cracks when applied below 5 °C. CW40-707’s ethylene segments act as internal plasticization, keeping the polymer intrinsically soft. Dynamic mechanical analysis (DMA) of a neat film cast and cured at +2 °C reveals a single glass transition at ‑12 ± 2 °C with a tan delta peak half‑width of 22 °C, indicating homogeneous phase behaviour rather than the dual‑Tg pattern signalling incompatible plasticizer domains. This allows poured‑in‑place waterproofing screeds to be applied at +3 °C surface temperature without post‑applied heating tents, a requirement documented in multiple Scandinavian infrastructure specifications aligned with BWR 15 (Swedish National Board of Housing). At these low temperatures, open time—defined here as the interval during which a fresh mortar bead can embed a ceramic tile to achieve 0.5 MPa pull‑off adhesion per EN 1348:2007—extends to 22 minutes, compared to 8–10 minutes for an SBR latex-modified mortar at equivalent polymer loading.
In submerged‑condition testing executed on 50 mm × 50 mm porcelain tile adhered to C30/37 concrete slabs with a 3 mm notched trowel bed, CW40-707 at a p/c of 0.30 delivered 1.7 MPa adhesion strength after 21‑day water immersion at 23 °C followed by 4‑hour ambient re‑conditioning, while failing cohesion was 100% within the substrate concrete rather than at the adhesive‑tile interface. By contrast, a standard VA/VeoVa copolymer emulsion yielded 1.1 MPa with a mixed cohesive/adhesive fracture pattern, and an uncarboxylated VAE of equivalent Tg registered 0.8 MPa with visible water‑blush at the bond line. These differences are attributed to the silane‑functional grafting that promotes moisture‑resistant bonding to siliceous aggregates in the concrete matrix. The comparison highlights why CW40-707 is specified in slip‑resistant swimming pool edging installations where water immersion alternates with UV exposure, a dual stress that rapidly debonds conventional polymer‑cement pastes.
Fresh Portland cement paste exhibits a pH above 13.2, a chemical environment sufficient to hydrolyze the ester side‑chains of many acrylic latexes, leading to loss of mechanical integrity within 28‑day wet storage. CW40-707’s ethylene‑rich backbone is fully saturated and resistant to alkaline saponification. Accelerated durability was verified by storing 40 mm × 40 mm × 160 mm mortar prisms containing 3.0 wt% polymer solids on cement weight in saturated Ca(OH)₂ solution at 50 °C for 30 days. Flexural strength retention, measured according to EN 196‑1, was 91% for CW40-707 formulations versus 62% for a commercially available all‑acrylic waterproofing emulsion of equivalent film hardness (Shore A 55 at 7‑day dry cure). This alkaline saponification resistance is particularly decisive in overlayment of freshly poured structural concrete where the residual moisture and alkali front persist for months. A common field failure observed in parking deck repair—blistering of the polymer‑cement overlay within 6 months of application—has been traced to glycolic ester degradation products that plasticize the acrylic film. CW40-707 does not generate these degradation fragments, making it suitable for high‑alkali overlay systems without a dedicated primer or pH‑suppressing surface treatment.
Comparative performance in a standardized external thermal insulation composite system (ETICS) basecoat demonstrates additional differentiation. Using a formulation consisting of CEM I 42.5R cement, 0.1–0.5 mm silica sand, and 2.5% polymer solids, a 5 mm basecoat reinforced with 160 g/m² alkali‑resistant glassfibre mesh was applied to expanded polystyrene (EPS) panels. After 28‑day cure at +23 °C / 50% RH followed by 24‑hour water immersion, the CW40-707‑based basecoat retained 0.12 MPa adhesive strength to EPS (failure in the insulation) per ETAG 004, while the reference acrylic-modified basecoat reached only 0.07 MPa with adhesive failure at the mortar‑EPS boundary. This 70% improvement in wet adhesion directly translates to fewer blow‑off events during rain‑wind weathering cycles according to on‑site pull‑off records collected on a 12‑storey residential façade in the Baltic region.
| Property | CW40-707 | Standard VAE (non-functionalized) | Pure Acrylic (Tg -10 °C) |
|---|---|---|---|
| Solids content (%) | 54.5 ± 1.0 | 55.0 ± 1.0 | 50.0 ± 1.0 |
| MFFT (°C, ISO 2115) | <0 | 0–2 | +18 (needs coalescent) |
| Water absorption of neat film (%, ASTM D 471, 24h immersion) | 4–6 | 18–25 | 8–12 |
| Adhesion after 7d water immersion (EN 1542, MPa) | 1.7–2.1 | 0.6–0.9 | 1.0–1.3 |
| Alkaline hydrolysis resistance (flexural strength retention, %) | 91 | 78 | 62 |
| Crack bridging ability at -5 °C (EN 1062-7, Class A3) | Passes at 0.75 mm | Passes at 0.35 mm | Fails below 0 °C |
In a production environment using continuously operated ribbon blenders for dry‑mix preparation followed by field mixing with a handheld paddle mixer, the shear stability of CW40-707 ensures that viscosity drift during recirculation through a piston pump is held below 10% over a 6‑hour working shift. This stability is monitored in‑line via a Brookfield AST‑100 online viscometer set to 25 ± 0.5 °C, a practice adopted at several pre‑bagged mortar plants in the Benelux region. A secondary effect of the carboxylation is enhanced dispersion of carbon black and iron oxide pigments, reducing colour float by an estimated 30% compared to non‑carboxylated VAE, though no standardized quantitative method currently exists for this specific metric in wet mortar; evaluation relies on spectrophotometric ΔE measurement per ISO 7724‑3 across five sampling points on a 300 mm × 300 mm trowelled panel.
Processing incompatibilities exist. Direct blending with amine‑based accelerators used in rapid‑setting repair mortars (e.g., those containing triethanolamine admixtures) causes premature flocculation, evidenced by a sharp rise in Brookfield viscosity from approximately 4,500 mPa·s to above 25,000 mPa·s within 90 seconds of mixing. Formulators must pre‑blend these accelerators into the dry cement powder phase rather than adding them to the liquid emulsion. Additionally, storage of CW40-707 below +2 °C for periods exceeding 72 hours can introduce ice‑crystal‑induced shear degradation that permanently reduces tensile elongation of the subsequently cast film by 15–20%; shipments subjected to freeze‑thaw must be tested for grit formation by filtration through a 45 μm sieve before use. At relative humidity above 85% during open‑time phase of tile adhesive application, skinning time shortens by approximately 40%, necessitating smaller working areas of roughly 1.0 m² per batch mix to avoid premature surface crusting invisible to the tiler before tile placement.