| HS Code | 248487 |
| Product Name | CW40-702 Medium-Viscosity VAE Emulsion |
| Appearance | White milky liquid |
| Solid Content | 40 ± 1% |
| Viscosity Brookfield Rvt 20 Rpm 25 C | 2500 ± 500 mPa·s |
| Ph | 5.0 ± 1.0 |
| Glass Transition Temperature Tg | -2°C |
| Minimum Film Formation Temperature Mfft | 0°C |
| Average Particle Size | 1.0 - 2.0 μm |
| Density At 25 C | 1.05 - 1.10 g/cm³ |
| Residual Vinyl Acetate Monomer | ≤ 0.1% |
| Freeze Thaw Stability | Stable for 5 cycles |
| Mechanical Stability | Excellent |
As an accredited CW40-702 Medium-Viscosity VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | CW40-702 Medium-Viscosity VAE Emulsion is supplied in 200 kg sealed plastic-lined steel drums, ensuring safe handling, stability, and easy dispensing. |
| Container Loading (20′ FCL) | Load 20′ FCL with drums/IBCs, secure tightly, avoid overloading, ensure compatibility and stability for safe transport. |
| Shipping | CW40-702 Medium-Viscosity VAE Emulsion ships in sealed drums, totes, or bulk tankers. Maintain temperature between 5–40°C; protect from freezing and excessive heat. Classified as non-hazardous, yet handle with standard chemical safety: avoid prolonged skin contact and ingestion. Keep containers upright, tightly closed, and away from oxidizing agents. Ensure ventilation during handling. |
| Storage | Store CW40-702 Medium-Viscosity VAE Emulsion in tightly sealed, original containers in a cool, dry, well-ventilated area. Maintain temperature between 5°C and 30°C; avoid freezing or excessive heat. Keep away from direct sunlight, sparks, and incompatible materials. Prevent contamination, and follow manufacturer shelf-life recommendations for optimal performance. |
| Shelf Life | Shelf life is 12 months from manufacture when stored unopened at 5–35°C, protected from frost and direct sunlight. |
The fabrication of Type II adhesive joints for non-structural wooden assemblies exposed to indoor humidity cycles and occasional water contact has long depended on the controlled coalescence behavior and film mechanics of vinyl acetate-ethylene (VAE) copolymer dispersions. CW40-702, with its manufactured minimum film-forming temperature (MFFT) of approximately 0°C and a Brookfield viscosity of 3000 mPa·s (RVT #4/20 rpm), enters a production workflow where the raw latex is first charged into a planetary dissolver equipped with a wall-scraper and butterfly paddle operating at 30–60 rpm. The addition sequence dictates the final colloidal stability and crosslink distribution: a defoamer based on mineral oil is introduced at 0.1–0.3 wt%, followed by a plasticizer-free thickener system (typically a combination of cellulose ether and polyurethane associative thickener) to achieve a final Brookfield viscosity of 20,000–50,000 mPa·s. The critical design question is whether hydrophobic crosslinking is required. Without a reactive isocyanate or zirconium ammonium carbonate additive, the coalesced VAE film yields sufficient dry adhesion to meet EN 204 D2 classification on beech, but the film reverts to a weak, swollen state after 4 days of cold water immersion at 23°C per EN 14257, generating shear strengths below 2 N/mm² and failing the D3 requirement. The incorporation of a polymeric methylene diphenyl diisocyanate (pMDI) crosslinker at 10–15 wt% of latex solids introduces a rheological and kinetic boundary: the mixture exhibits a pot-life limitation of 45–90 minutes at 20°C, defined by a doubling of Brookfield viscosity as measured under ASTM D3236. This window shortens to less than 30 minutes at 30°C, a frequent failure mode observed on production lines where static mixers feed roller coaters without jacketed cooling. The optimum pH buffer zone for the blend is maintained at 6.5–7.0 with sodium bicarbonate prior to crosslinker introduction, since lower pH accelerates isocyanate hydrolysis and carbon dioxide evolution, creating microfoam that weakens the bond line. Fully cured films from such crosslinked formulations under cold press at 0.7–1.0 MPa yield characteristic lap-shear values above 10 N/mm² (EN 205) and, critically, maintain wood failure percentages exceeding 80% after both the 4-day cold-water soak (D3) and the 6-hour boiling-water immersion plus 2-hour cooling in water (D4) according to EN 204. The formulated adhesive is transferred to a roll coater with a doctor blade gap set to deliver 150–200 g/m² onto hardwood lamellae. Finished assemblies cover high-frequency laminated beams, three-layer engineered parquet flooring, and finger-jointed non-structural frames. A major operational boundary is that crosslinked formulations are incompatible with amine-based catalysts and must be protected from frost during transport, since freeze-thaw cycles above three cycles can induce irreversible grit formation and loss of open time. Table 1 summarizes the typical performance envelope observed when CW40-702 is formulated with and without a pMDI crosslinker under EN 204 test regimes.
| Formulation configuration | Crosslinker dosage (wt% on latex solids) | EN 204 durability class achievable | Dry shear strength (N/mm²) | Wet shear after 4 d cold water (N/mm²) | Wet shear after 6 h boiling (N/mm²) |
|---|---|---|---|---|---|
| VAE only (CW40-702 neat) | 0 | D2 | 10–12 | ≤1.5 (fail) | Not testable |
| VAE + pMDI, low crosslink | 5–8 | D3 | 11–14 | 4–6 | ≤2 (fail) |
| VAE + pMDI, optimized | 10–15 | D4 | 12–16 | 7–9 | 4–6 |
The polymer modification of hydraulic binders for flexible waterproofing slurries depends on the interplay between portland cement hydration and the formation of a continuous polymer film within the capillary pores. CW40-702 is introduced into the liquid component of a two-component system alongside water and a small amount of plasticizer or defoamer, to be mixed on-site with a powder blend of grade 42.5R ordinary portland cement, silica sand with a top size of 0.3 mm, and a powdered polycarboxylate superplasticizer. The polymer-to-cement ratio (p/c) by dry solids is the primary lever governing the transition from a rigid mortar to a flexible waterproofing membrane. Industry specifications such as GB/T 23445-2009 Type II and JC/T 984-2011 Type I require a balance of tensile adhesion strength above 0.7 MPa after wet conditioning, and elongation at break exceeding 80% for films. With CW40-702, a p/c ratio in the range 0.05–0.10 (corresponding to approximately 90–180 kg of the commercial 55% solids emulsion per tonne of dry mix, assuming a liquid-to-powder mass ratio of 0.4) mainly improves workability and resistance to microcracking, while p/c values between 0.10 and 0.20 shift the cured composite into a rubber-like regime where elongation can be tuned between 40 and >150% and crack-bridging ability under JC/T 984 reaches 2–3 mm. The mixing equipment must be low-shear: a 300–500 rpm paddle mixer with a toothed disc minimizes air entrapment that would otherwise nucleate pinholes and reduce the wet-film waterproofing integrity. The mixed slurry is typically applied by notched trowel or airless spray in two orthogonal coats to a total dry film thickness of 1.5–2.0 mm. A frequently encountered processing conflict is the sensitivity of VA-E emulsion to divalent cations liberated during cement hydration; at p/c ratios above 0.20, a delayed release of calcium ions can cause local coagulation of the latex, observed as a “grainy” surface finish and a drop in peel adhesion on damp concrete substrates. The standard quality-control protocol includes a wet adhesion test according to GB/T 16777, where the coating is applied to a cementitious slab and immersed for 168 hours before pull-off testing. Table 2 maps the dependence of critical mechanical parameters on p/c ratio for a typical CW40-702-based liquid component mixed at a water-to-cement ratio of 0.35.
| p/c ratio (dry polymer/cement) | Compressive strength (28 d, MPa) | Flexural strength (28 d, MPa) | Tensile adhesion to concrete (7 d dry + 7 d wet, MPa) | Elongation at break (%) | Crack-bridging capability (mm) |
|---|---|---|---|---|---|
| 0.05 | 35–40 | 8–10 | 0.8–1.0 | 20–30 | 0.5–0.8 |
| 0.10 | 22–28 | 10–13 | 1.0–1.4 | 60–90 | 1.5–2.0 |
| 0.15 | 14–18 | 12–15 | 1.2–1.6 | 120–160 | 2.5–3.0 |
| 0.20 | 8–12 | 12–14 | 1.0–1.3 | >180 | >3.0 (limited film cohesion) |
Laminating porous cellulosic substrates for multi-wall sacks, envelope windows, and folding cartons calls for an aqueous adhesive that delivers rapid fiber tear on setting without the plasticizer migration concerns associated with polyvinyl acetate homopolymers. CW40-702, as an unplasticized VAE latex, is typically used at the 95–100% solids fraction in the adhesive compound, with the remaining balance comprising a defoamer, a wetting agent (e.g., dioctyl sulfosuccinate, <0.1 wt%), and occasionally 0.5–2.0 wt% of a borate-modified dextrin to extend open time on high-speed rotary cut-off laminators. At a dry coating weight of 3–5 g/m², applied via a grooved roll or air-knife coater, the emulsion sets within 2–5 seconds under light compression, providing initial fiber tear to kraft linerboard at >90% area. For indirect food contact, the formulation components must be selected from positive lists such as FDA 21 CFR §176.170 (Components of Paper and Paperboard in Contact with Aqueous and Fatty Foods) and Regulation (EU) No 10/2011 Annex I. The absence of external plasticizers and of alkylphenol ethoxylate surfactants in the CW40-702 manufacturing simplifies the regulatory dossier. The bonded articles—dry food sachets, cement bag valves, envelope closing seams—pass accelerated aging tests at 60°C for 48 hours without delamination. The main operational boundary is that the freshly coated web must not be exposed to relative humidity above 85% before rewinding, as residual water plasticizes the film and leads to blocking.
Reducing indoor air volatile organic compound (VOC) loads in high-build interior wall paints demands a binder that can form a coherent, scrub-resistant film without the assistance of volatile coalescing agents. CW40-702, defined by an MFFT of 0°C and a moderate polymer glass transition temperature near +3°C, enables a zero-VOC architectural coating when formulated at a pigment volume concentration (PVC) range of 55–65% in a matte formulation, dropping to 40–50% PVC in a low-sheen variant. The coating compound is manufactured in two stages: a high-speed Cowles disperser running at a tip speed of 18–22 m/s incorporates titanium dioxide (rutile, R-996 grade) and a coarse calcium carbonate extender (10 µm median diameter) into an aqueous solution of a sodium polyacrylate dispersant (active on solids 0.2–0.5%) and a defoamer based on polysiloxane; this is followed by a low-shear let-down phase where CW40-702 is added at a dosage such that the binder solids constitute 13–18% of the total formulation weight. The rheological profile is then adjusted using a hydroxyethyl cellulose thickener to a Stormer viscosity of 95–105 KU and an ICI cone-and-plate viscosity of 1.5–2.5 poise. This combination ensures good brush loading with minimal spatter under ISO 1518-1 scrub resistance testing, where the cured film after 28 days must withstand ≥200 cycles on a scrub machine before breakthrough. The critical compliance benchmarks are GB/T 9756-2018 for synthetic resin emulsion interior coatings and JG/T 481-2015 for low-VOC water-based coatings, the latter requiring a TVOC content below 50 g/L. CW40-702-based formulations without freeze-thaw additives risk syneresis after repeated freeze-thaw cycles; standard practice is to blend with an acrylic protective colloid emulsion at 5–10% on resin solids if product storage below -5°C is anticipated.
Bonding cellulose fluff and superabsorbent polymer (SAP) particles within the acquisition-distribution layer of an ultra-thin infant diaper core requires an adhesive that gives a soft, non-abrasive hand feel and maintains fiber-bond integrity under warm, saline humidity. CW40-702, diluted with demineralized water to a solids content of 20–25%, is sprayed through a series of air-assisted slot nozzles (nozzle gap 0.2–0.3 mm, atomizing air pressure 0.3–0.5 bar) directly onto the formed nonwoven web running at speeds of 300–600 m/min. The dry add-on is controlled within a narrow window of 2–5 g/m² to avoid stiffening the cellulose matrix. The applied latex must achieve sufficient wet cohesion to prevent SAP migration during the rewetting cycles described in NWSP 070.1 (liquid strike-through time) and EDANA standard test 401.0-89. Because CW40-702 retains a degree of water swellability, the bond fails gradually rather than undergoing brittle delamination, which maintains core pad integrity in a butt-weld configuration. The emulsion’s compatibility with rosin ester tackifiers is exploited when a peel strength above 0.3 N (as per the 180° T-peel on NWSP 400.1) is required for bonding a spunbond polypropylene topsheet to the acquisition layer; a tackified CW40-702 blend at 5% tackifier addition can be applied by spiral spray to reduce the bond area to 15–30% coverage, preserving breathability. The operational limitation is that the spray nozzles must be cleaned with a water flush every 4–6 hours to prevent nozzle plugging from dried film, a downtime that integrators document as the primary cause of basis-weight drift in high-speed converting lines.
The formulation of a water-based architectural joint sealant that meets the low-modulus, high-movement specification of ISO 11600 Type 25 LM begins with the preparation of a high-solids paste in a vacuum-equipped double planetary mixer. CW40-702 is blended with an anionic acrylic copolymer emulsion in a 40:60 to 60:40 solids ratio to achieve a balance between low-temperature flexibility and surface tack-free time. The binder blend, which constitutes 30–35% of the total wet weight, is combined with a stearate-coated ground calcium carbonate filler (average particle diameter 5–8 µm) at 45–50% loading, a phthalate-free plasticizer (e.g., diisononyl adipate) at 2–4%, and a fibrillated cellulose or fumed silica thixotrope at 0.5–1.0% to confer a slump resistance exceeding 2 mm per ASTM D2202. The addition sequence is critical: the filler must be incorporated under vacuum of -0.08 MPa after the binder and plasticizer have been premixed for 15 minutes at 60 rpm, to prevent air voids that weaken the cohesive strength tested at 100% extension per ASTM C719. The cured bead typically achieves a Shore A hardness of 20–30 after 21 days at standard conditions (23°C, 50% RH), with a movement accommodation factor exceeding 25% of the original joint width. The filled sealant is dispensed through a pneumatic caulking gun into a butt-joint on anodized aluminum for peel adhesion testing under ASTM C794; wet adhesion values above 5 N/mm are routinely recorded provided the CW40-702 fraction does not exceed 60% of the total binder, above which the sealant surface exhibits excessive residual tack and collects dirt. This tack limit represents the inherent incompatibility of pure VAE films with exterior weathering in continuously wet climates, but for indoor perimeter joints and window-frame sealing, the CW40-702-containing compound yields a low-VOC, paintable joint filler compliant with ASTM C834 Type OP.
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| Property | Value | Test method |
|---|---|---|
| Viscosity (mPa·s, 20 rpm, spindle 4) | 2,800–3,400 | ISO 2555:2018 |
| Solids content (wt%) | 55.0 ± 1.0 | ISO 3251:2019 |
| pH | 4.5–5.5 | ISO 976:2013 |
| Density at 20°C (g/cm³) | 1.07 | ISO 2811-1:2016 |
| Minimum film-forming temperature (°C) | ±0 | ISO 2115:2000 |
| Tg (MDSC midpoint, °C) | +5 | ISO 11357-2:2020 |
| Residual ethylene (mol%) | 12–14 | Internal GC headspace |
| Mechanical stability (Marlon A/10 min) | <0.5% coagulum | ISO 2006:2013, modified |
| Substrate | Peel strength (N/cm) | Failure mode |
|---|---|---|
| Stainless steel 304, 2B finish | 4.1 | Cohesive |
| Polypropylene, corona-treated (44 mN/m) | 2.8 | Interfacial/light cohesive |
| LDPE, untreated | 0.9 | Adhesive |
| Glass, air side | 5.7 | Cohesive |
| Beechwood, planed, 12% moisture | 6.3 | Substrate failure (>80% fiber tear) |