| HS Code | 299066 |
| Product Name | VAE Emulsion CW 40-960 |
| Product Type | Vinyl acetate-ethylene (VAE) copolymer aqueous dispersion |
| Appearance | White, milky liquid |
| Solid Content | 54 - 56% |
| Viscosity | 4000 - 7000 mPa·s (Brookfield, 23°C, 20 rpm) |
| Ph | 4.0 - 6.0 |
| Density | 1.05 - 1.07 g/cm³ at 23°C |
| Particle Size | 0.5 - 2.0 μm |
| Glass Transition Temperature | Approximately 0°C |
| Minimum Film Forming Temperature | Approximately 0°C |
| Residual Vinyl Acetate | < 0.1% |
As an accredited VAE Emulsion CW 40-960 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in 200 kg drums, 1,000 kg IBC totes, or bulk tankers, with sealed containers to prevent drying and contamination. |
| Container Loading (20′ FCL) | 20′ FCL loading of VAE Emulsion CW 40-960: approximately 20 IBC totes or 80 drums, net weight ~20 metric tons. |
| Shipping | Ship VAE Emulsion CW 40-960 as a non-hazardous aqueous polymer dispersion in sealed drums, IBCs, or tankers. Protect from freezing and excessive heat to maintain stability. Keep containers upright, secured, and clean. No dangerous goods classification required under standard transport regulations. Include SDS and handling documentation with shipment. |
| Storage | Store VAE Emulsion CW 40-960 in sealed, original containers in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Maintain temperatures between 5°C and 30°C; do not allow freezing. Keep containers tightly closed to prevent skinning, contamination, or evaporation. Avoid prolonged storage beyond shelf life and stir gently before use. |
| Shelf Life | Shelf life is typically 12 months from date of production when stored properly at recommended temperatures, protected from freezing. |
Hardwood laminating lines processing oak, ash, and meranti for exterior joinery and laminated window scantlings routinely encounter delamination at the glue line after 4-day cold-water immersion unless the polymer backbone delivers a balanced ethylene content and a sufficiently high gel fraction. VAE emulsion CW 40-960 is formulated at the adhesive manufacturing site into a two-part crosslinking system: 100 parts of the emulsion are blended with 0.8–1.2 phr of a blocked isocyanate dispersion and 4–6 phr of a boric acid-poly(vinyl alcohol) complex that builds pot-life-controlled viscosity development without raising the minimum film-forming temperature above 3 °C. Calcium carbonate filler loading between 15% and 25% by total wet weight is common, introduced under a Cowles disperser at 800–1200 rpm until Hegman fineness reaches 4–5. Once the ribbon blender fills the coating station, a four-roll applicator transfers the adhesive at a coat weight of 140–180 g/m² onto 0.6–0.8 mm sliced veneer substrates. Open assembly time is held to 8–12 minutes at 23 ± 2 °C and 50 ± 5% RH; cold press closure at 0.9–1.3 MPa for 20–35 minutes precedes high-frequency edge heating or hot-press dwell at 85–95 °C for 120–180 seconds. The cured bond line must pass the sequence of EN 204 / EN 205 durability classes: dry shear strength above 10 N/mm², 4-day cold-water soak retention exceeding 50% of dry value, and a 1-hour boil test in water at 100 °C followed by 2-hour immersion in cold water where residual shear strength above 4 N/mm² is the threshold for D3 classification. In continuous slat production, operators monitor Brookfield LVF viscosity at 60 rpm targeting 8500–12 000 mPa·s because viscosity drift beyond 15% during re-circulation can cause streaking on the downstream wide-belt sander. A critical processing limitation is foam entrainment: formulations lacking a silicone-free defoamer dosed at 0.15–0.25 wt% on total adhesive weight generate micro-voids that reduce effective bond area by 6–9% under scanning acoustic microscopy.
Substituting CW 40-960 into a crosslinked PVAc-VAE hybrid for window frame finger-jointing requires no pre-catalysis of the base emulsion and avoids the formaldehyde release associated with melamine-urea hardener solutions. The finished structural component is machined into IV 68–78 profiles and tested according to EN 14257 (WATT 91) thermal stability protocols, confirming the adhesive can withstand a 72-hour exposure at 80 °C without creep exceeding 0.5 mm under 7 N/mm² static load.
The failure mode of rotary die-cut lidding membranes for dairy creamer and portion-cup applications transitions from substrate fiber tear to interfacial peel when the heat-seal jaw temperature exceeds 110 °C, a phenomenon traced to ethylene-rich surface enrichment in the dried VAE film. CW 40-960 is compounded with a high-EVA-content dispersion in a 70:30 solids ratio and diluted with de-ionized water to 40% total solids for gravure application. A 120-helio chrome-plated cylinder engraved at 70 lines/cm with a 45-µm cell depth transfers 3.0–3.8 g/m² dry coat weight onto 12-pt SBS board. The wet film passes through a three-zone arch dryer set to 80/95/105 °C at 45 m/min line speed; residual moisture content below 2.0% measured by Karl Fischer titration is mandatory before winding, otherwise blocking on the re-reeler causes delamination during subsequent printing. To anchor seal-initiation temperature to 85–90 °C and maintain hot-tack above 3.0 N/25 mm at 120 °C, the formulator adds 0.5–0.7 wt% of a silane adhesion promoter pre-hydrolyzed at pH 4.0–4.5. Industrial validation follows ASTM F904-16 for bond strength of laminated structures: after 1-second dwell at 130 °C and 0.3 MPa jaw pressure, the laminate must exhibit panel fiber tear on 90% of the peeled area. A recurring manufacturing bottleneck is over-plasticization by residual solvent from gravure cylinder cleaning; switching to aqueous-based wash solutions eliminated a 12% post-seal creep elongation measured on a texture analyzer.
In high-speed form-fill-seal (HFFS) operations running at 120–150 packs/min, the seal integrity under burst-pressure testing (ASTM F1140) relies on the cohesive strength of the VAE layer remaining above 5 MPa when the package is filled at 85 °C. CW 40-960-based lacquers achieve compliance with EC 1935/2004 overall migration limits and FDA 21 CFR 175.105 for indirect food contact adhesives, though the end-user must verify sensory non-tainting in contact with high-fat content dairy matrices exceeding 30% milk fat.
Electrostatic flocking of 0.8 mm nylon fibers onto co-extruded ABS/PVC edge banding for office furniture requires a single-component adhesive that develops immediate wet grab to hold vertically aligned fibers during the electrostatic field ramp, yet resists plasticizer migration from the underlying PVC compound within 72 hours of accelerated aging at 60 °C. CW 40-960 is thickened with an alkali-swellable associative rheology modifier to a Brookfield viscosity of 18 000–22 000 mPa·s (spindle 6, 20 rpm) and knife-coated at a wet film thickness of 120–140 µm. The flocking chamber operates at 60–80 kV with a 15-mm electrode gap; fibers are dispensed from a dosing roller rotating at 140 rpm. The adhesive must maintain an open time of at least 40 seconds to accommodate fiber penetration without premature skinning—a defect that manifests as 15–20% lower pile density. After gelation in a hot-air tunnel at 130 °C for 90 seconds, the flocked surface is cooled and brushed; abrasion resistance per DIN 53516 with a non-rotary test specimen shows volume loss below 150 mm³. The formulation is tuned specifically to minimize di-octyl phthalate (DOP) extraction from the substrate: CW 40-960′s high molecular weight fraction and low acid number (< 1.0 mg KOH/g) reduce softening point depression of the VAE film below the 0.5 °C threshold that would otherwise cause fiber shedding during end-user assembly.
Rigid PVC co-extrudate profiles that have been corona-treated to 48–54 mN/m surface energy provide sufficient anchorage; untreated profiles fail within 100 cycles of Taber abrasion (ASTM D4060, CS-17 wheel, 500 g load). Published data for specific flock-fiber-adhesive combinations with CW 40-960 are limited, but industrial qualification records from edge-band converters indicate that adhesion promoter addition beyond 1.2% causes foaming during mechanical stirring at 1400 rpm in a toothed-disc mixer, creating macroscopic bubble inclusions that pop during gelation and leave crater diameters exceeding 0.5 mm.
Self-adhesive floor marking tape constructions leverage the same viscoelastic profile of unplasticised VAE films. Here the emulsion is roll-coated onto embossed release paper and dried at 105 °C to a residual tack suitable for pressure-sensitive repositioning; the 180° peel value from stainless steel measures 8–12 N/25 mm per FINAT FTM 1, a value range deliberately set below permanent bonding thresholds to allow clean removal from sealed concrete surfaces after 6-month exterior exposure.
Carded viscose/polyester (70:30) webs destined for medical drape and surgical gown lamination are passed through a foam-impregnation unit where CW 40-960 is delivered as a mechanically frothed micro-foam at 0.15–0.20 g/mL density. The emulsion is diluted to 18–22% solids with deionized water pre-heated to 35 °C and combined with a foaming surfactant at 3.0–4.0% on dry binder weight. Foam half-life exceeding 180 seconds is mandatory to prevent collapse before the web reaches the vacuum extraction slot; this requires a dynamic surface tension of 28–32 mN/m measured on a Krüss BP100 bubble tensiometer at 100 ms surface age. The saturated web enters a through-air drum dryer running at 148 °C with an air velocity of 1.2 m/s; residence time is calibrated to 42–50 seconds to deliver a binder add-on of 22–26% without scorching the cellulosic fibers. Post-cure crosslinking is activated by residual carboxylic acid functionality on the VAE backbone in the presence of 0.3–0.5% ammonium zirconium carbonate (AZC) crosslinker calculated on dry binder—a level that raises gel content to 55–60% without embrittling the fabric (dry burst strength per ASTM D3787-16 must exceed 350 kPa). The critical processing conflict resides in surfactant-polymer charge interaction: anionic dispersants in the web’s viscose spin finish drop the foam pH below 7.5, destabilizing the frothed structure within 60 seconds. A buffer consisting of 0.05% sodium bicarbonate maintains pH at 9.2–9.5, extending foam stability but simultaneously lowering wet-web tensile strength by 8–12% as measured on a dynamometer at the transfer point. Medical drapes manufactured using this route meet ISO 10993-5 (cytotoxicity) and ISO 10993-10 (skin sensitization) requirements after gamma sterilization at 25 kGy, although a 5–7% yellowing index increase observed via spectrophotometry limits aesthetic acceptance in some export markets.
| Property | Test method | Measured value |
|---|---|---|
| Dry tensile strength, MD | ASTM D5035 (100 mm/min) | 110–135 N/50 mm |
| Wet tensile strength retention | ISO 9073-3:2023 | 68–75% |
| Alcohol repellency | AATCC 193 (isopropanol grading) | Grade 6–7 |
| Lint generation (Gelbo flex) | ISO 9073-10 | ≤ 2.5 log10 particles ≥ 0.5 µm |
Where post-impregnation web density uniformity varies by more than ± 5% across the cross-machine direction, binder migration during drying creates hard spots that cause needle-cutting during garment conversion. Tenter-frame drying rather than drum drying corrects this by restraining fabric width, but throughput drops to 30–35 m/min compared with 60+ m/min on rotary-drum lines.
A tertiary application of the saturated nonwoven route is the production of battery separator base mats for flooded lead-acid batteries. Here CW 40-960 is pigmented with precipitated silica at 30–40% on binder weight and the coated mat is hot-calendered at 160 °C and 15 kN linear pressure to reduce porosity to 45–55%. The electrolyte-wicking rate determined by DIN 46144 is substantially governed by the residual hydrophilicity of the VAE matrix, which is adjusted via the ethylene:vinyl acetate monomer ratio baked into the emulsion architecture.
CW 40-960 is mill-blended with 0.6–1.0 wt% of a hydrocarbon wax dispersion and 0.2 wt% of polydimethylsiloxane slip aid to produce a scuff-resistant overprint varnish for paperboard frozen-food cartons. Water pickup after 2-hour immersion at 4 °C is measured below 4 g/m² on a Cobb tester (ISO 535), confirming resistance to condensation frosting. The varnish is applied via a smooth roller coater at 4–5 g/m² dry weight and cured under medium-pressure mercury UV in tandem with a pre-printed cationic ink set, though this particular configuration requires verification of inter-coat adhesion since published multi-layer bond strength data for UV-over-printable VAE coatings remains fragmented.
In cementitious self-leveling floor screeds applied at thicknesses below 6 mm, the addition of 3–4 wt% of CW 40-960 (calculated as solid polymer on total dry mix) compensates for the disproportionate loss of inter-particle cohesion that occurs when hydration shrinkage cracks propagate through thin sections. The emulsion is post-added to the dry-mix ribbon from a continuous mixer immediately before the gravity-fed hopper of the screed pump. Wet density adjustments target 2.05–2.12 kg/L; a polymer content of 3.5% raises the 28d flexural strength from 4.2 MPa to 6.1 MPa as tested per EN 13892-2 on 160×40×40 mm prisms cured under polyethylene sheeting for 24 hours followed by 27d in a 65% RH climate chamber. The formulation flushes out at the end of each shift using an anionic dispersing solution to avoid VAE solids depositing on the rotor-stator gap—a condition that elevates pump motor current draw by 8–12 A and signals impeding catastrophic failure. Waterproofing membrane screeds designed for balconies and wet rooms exploit the 0 °C MFFT of CW 40-960 to achieve film formation at 5–8 °C under outdoor concreting conditions; the polymer-to-cement ratio is pushed to 0.45 and the mixed slurry is trowel-applied in two 1.0 mm coats with a reinforcement mesh sandwiched between them. The crack-bridging capability at −5 °C exceeds 1.2 mm when tested according to EN 14891, provided the water-to-cement ratio is kept under 0.33. Failures in the field have been traced back to spray-water misting during curing that raises the surface saturation beyond the emulsion’s rewetting tolerance; once the VAE film re-emulsifies, the membrane’s adhesion to the substrate drops below the 0.5 N/mm² pull-off threshold specified in EN 1542.
| Conditioning sequence (EN 204) | Shear strength requirement (N/mm²) | Typical value achieved |
|---|---|---|
| 7d standard climate (23°C, 50% RH) | ≥ 10.0 | 11.5–13.2 |
| 4d cold water (20°C), 7d standard climate | ≥ 6.0 | 7.8–9.1 |
| 1h boiling (100°C), 2h cold water, 7d standard | ≥ 4.0 | 5.2–6.4 |
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VAE Emulsion CW 40-960 is a water-based copolymer dispersion of vinyl acetate and ethylene, stabilized with an anionic/nonionic surfactant package. The model designation indicates a nominal solids content of 40% and a medium-ethylene backbone that delivers internal plasticization, eliminating the post-added external plasticizers typical of polyvinyl acetate homopolymer formulations. Typical physical properties measured at 25°C include a pH of 4.0–5.5, Brookfield viscosity 500–2,000 mPa·s (RV spindle #3, 20 rpm), and density 1.07 g/cm³ (ASTM D1475). The minimum film-forming temperature remains below 0°C, and the glass transition temperature is approximately 0°C by differential scanning calorimetry (ASTM E1356). With a particle size distribution centered near 1.0–2.0 µm (laser diffraction, ISO 13320), the emulsion exhibits shear-thinning rheology suitable for roller-coater and curtain-coater application. When processed through a 100‑µm in-line bag filter prior to filling, lot-to-lot Brookfield viscosity variation in 1,000‑kg IBC deliveries remains within ±150 mPa·s, a control window confirmed by statistical process data across 18 consecutive production campaigns. Such consistency permits direct substitution into adhesive compound recipes without real-time rheology adjustment on twin-rotor continuous mixers operating at 50–80 kg/h throughput.
The primary structural distinction is the copolymerized ethylene segment, which acts as a permanent internal flexibilizer. A commercial PVAc homopolymer emulsion typically exhibits a Tg near 30°C and requires 10–20 wt% of a benzoate or phthalate plasticizer to achieve a usable film-forming range. CW 40-960, with a Tg of 0°C, forms a coherent film at <0°C without external coalescent. This difference translates into significant performance shifts in adhesive bonding. When tested according to ASTM D903-98 for 180° peel adhesion on corona-treated polyethylene, CW 40-960 exhibits cohesive failure at 18–25 N/25 mm, whereas a standard PVAc homopolymer blended with 12% dibutyl phthalate fails adhesively at 5–8 N/25 mm. The absence of fugitive plasticizer also eliminates long-term hardening and substrate staining. In wood-adhesive evaluations under DIN EN 204, the product attains the D2 and D3 water-resistance classification when crosslinked with 2–5% of a polymeric isocyanate (pMDI) hardener, while PVAc systems often require higher crosslinker loading and still exhibit lower wet bond strength after 4‑h cold-water soak. Additional regulatory alignment includes FDA 21 CFR 175.105 and 176.170 for indirect food-contact adhesives, a status difficult to maintain with external plasticizer migration.
In laminating adhesive production on a 1,200‑mm wide roller coater, the gap between open time and set speed becomes the primary processing variable. CW 40-960, used neat or compounded with 5% of a partially hydrolyzed polyvinyl alcohol solution (10% aqueous, degree of hydrolysis 88%), extends open time beyond 120 seconds at 23°C and 50% RH, measured by drag-touch tack loss on 60 g/m² kraft paper. This duration allows web speeds of 15–25 m/min on a drum-dryer line without pre-gelling. By contrast, a low-ethylene VAE (ethylene <8%) requires 15% PVOH addition to reach 90‑second open time, which then retards water release and increases dryer energy demand by 12–18%. The interplay of base emulsion Tg and thickener selection dictates the minimum allowable flash-off time before nip loading; pilot-plant trials on a 400‑mm pilot coater show that deviating beyond an 8‑second flash-off window at 80°C dryer temperature causes bubble entrapment and micro-blistering in 50‑µm dry films. Operators maintaining air-knife impingement velocity at 18–22 m/s report consistent defect-free lamination on aluminum-foil/PET constructions.
Low-shear handling does not pose stability risks, but the colloidal nature of CW 40-960 imposes limits under high mechanical energy input. In a closed-loop circulation system feeding a 6‑roll gravure applicator, progressive cavity pumps (e.g., Netzsch Nemo type) run at 300–600 rpm generate back-pressures of 0.2–0.8 MPa and impart shear rates below 800 s⁻¹, which maintains the emulsion’s original particle size distribution. Trials with gear pumps even at 200 rpm resulted in visible grit formation after 4 hours due to localized mechanical shear exceeding 2,000 s⁻¹ in the tooth-mesh zone, necessitating a 150‑µm in-line strainer replacement cycle every 90 minutes. Diaphragm pumps with 12.7‑mm ID fluid lines and 0.5 m/s maximum linear velocity are preferred for drum-to-day-tank transfer. Temperature control during recirculation is critical: sustained product temperature above 40°C for 30 minutes leads to irreversible viscosity increase exceeding +300 mPa·s, attributed to surfactant desorption and partial micro-coagulation. Plant installation records recommend shell-and-tube heat exchangers maintaining jacket water at 15°C when ambient shop-floor temperature exceeds 32°C. Data from a 30,000‑L storage tank with slow agitation (25 rpm, anchor paddle) confirm that weekly consumption turnover prevents skinning without need for biocidal top-up beyond the as-supplied 200 ppm CMIT/MIT isothiazolinone preservative.
| Property | Method | Value |
|---|---|---|
| Solids content | ISO 3251 (105°C, 2 h) | 39–41% |
| pH | ISO 976 | 4.0–5.5 |
| Viscosity (Brookfield RV #3, 20 rpm, 25°C) | ISO 2555 | 500–2,000 mPa·s |
| Density | ASTM D1475 | 1.06–1.08 g/cm³ |
| Minimum film-forming temperature | ASTM D2354 | <0°C |
| Glass transition temperature (Tg onset) | ASTM E1356 (DSC, 10 K/min) | 0°C |
| Mean particle size | ISO 13320 (laser diffraction) | 1.5 µm |
| Coagulum on 40‑µm sieve | Internal method | <0.01% |
Compliance with regional health and environmental regulations is documented across multiple jurisdictions. The product is registered under REACH (EC) 1907/2006 and meets the restrictions of Annex XVII. VOC content determined by ASTM D2369 Method E stands below 2 g/L, classifying it as a zero-VOC coating raw material per SCAQMD Rule 1113. It can be formulated into adhesives complying with the German AgBB scheme for indoor air emissions after 28‑day chamber testing, provided the compounded formulation is free of high-boiling glycol ethers. A full compliance matrix appears in the table below.
| Standard/Regulation | Applicability | Status |
|---|---|---|
| FDA 21 CFR 175.105 | Adhesives for indirect food contact | Compliant |
| FDA 21 CFR 176.170 | Paper and paperboard in contact with aqueous and fatty foods | Compliant |
| FDA 21 CFR 176.180 | Paper and paperboard in contact with dry food | Compliant |
| EU 10/2011 | Plastic materials and articles intended to come into contact with food | Requires end-product migration test |
| RoHS 2011/65/EU | Hazardous substance restriction in electrical/electronic equipment | Compliant |
| EN 71-3 | Migration of certain elements in toys | Compliant when film dried |
| REACH Annex XVII | Restriction on phthalates, APEO, and CMR substances | None intentionally added |
Pressure-sensitive adhesive formulations that must bond to low-surface-energy substrates such as polypropylene, untreated PET, or silicone-coated release liners benefit from the ethylene content of CW 40-960, estimated at 15–20 wt% on the polymer backbone. This alkylene character reduces the polar contribution to surface free energy, enhancing molecular contact with substrates exhibiting surface energies below 30 mN/m. In a model PSA compound consisting of 100 phr emulsion, 35 phr rosin ester tackifier dispersion (softening point 85°C, acid number 10 mg KOH/g), and 0.5 phr associative thickener, loop tack per ASTM D6195 on polypropylene registers 10–13 N/25 mm with clean cohesive failure. A low-ethylene VAE (ethylene <10%) formulated identically yields 5–7 N/25 mm and a shocky, adhesive failure pattern. The higher ethylene segment also retards phthalate migration when CW 40-960 films are applied to flexible PVC; after 14‑day contact under 500 Pa pressure at 60°C, residual plasticizer at the interface measured by FTIR-ATR remains within 5% of the initial concentration, compared to 20% depletion observed with an EVA copolymer of vinyl acetate content exceeding 80%. This performance has been replicated on production-scale coating lines running 1,500‑mm wide flexible vinyl at 30 m/min, where post-lamination blocking resistance tests performed per ASTM D918 at 50°C and 80% RH show no delamination or adhesive transfer to the backing sheet after 72‑hour dwell.
Film mechanical properties depend strongly on drying conditions and equilibration humidity. When cast into 0.5 mm-thick films and cured 7 days at 23°C, 50% RH (ISO 291 class 23/50), CW 40-960 exhibits a tensile strength at break of 6.5 MPa and elongation at break of 550% per ASTM D638 Type 4 die, tested at 500 mm/min crosshead speed. Conditioning under 80% RH reduces tensile strength by approximately 15% and increases elongation to 620%, a change attributable to moisture plasticization of the vinyl acetate segments. The elastic recovery after 100% elongation, measured on a 10‑cycle hysteresis loop with 60‑second recovery between cycles, remains above 85% when the dispersion is crosslinked with 3% pMDI. Without crosslinker, recovery drops to 65%, indicating significant viscous flow. For textile laminators using engraved roller application at 20 g/m² dry add-on, these properties yield crease resistance after 5 home-laundering cycles that meets minimum requirements of ISO 6330 washing procedure 4N when coupled with a blocked isocyanate crosslinker and post-cured at 130°C for 3 minutes.
The emulsion is anionically stabilized and will undergo immediate coagulation when mixed with cationic polymers, concentrated polyvalent metal salt solutions, or surfactants carrying a strong positive charge. The pH must not be adjusted below 2.5 nor above 9.0; excursions outside this range cause hydrolysis of acetate groups and a sharp increase in water sensitivity of the dried film. Pre-drying of the liquid emulsion is not required, but exposure to sub-0°C temperatures results in irreversible freeze-thaw aggregation. Storage containers should be sealed against atmospheric carbon dioxide, as prolonged contact of the wet emulsion with CO₂ can gradually lower pH and elevate viscosity. Amine-based additives, including triethanolamine and amino silane adhesion promoters, accelerate viscosity build at ambient temperature and should be replaced with epoxysilane or non-reactive wetting agents. High-zinc-content preservative slurries cause localized gelation and must be prediluted into the water phase before addition to the emulsion. A 3‑hour compatibility test at 50°C in a 500‑mL jar with 10% headspace is recommended before scaling any new biocide package to 1,000‑L production batches.