| HS Code | 974151 |
| Chemical Composition | Vinyl acetate-ethylene copolymer |
| Appearance | Milky white liquid |
| Solids Content | 55 ± 1 |
| Viscosity Mpa S | 1500 - 2500 |
| Ph | 4.5 - 6.0 |
| Glass Transition Temperature Degc | -5 |
| Minimum Film Forming Temperature Degc | 0 |
| Particle Size Um | 0.2 - 1.0 |
| Density G Cm3 At 20c | 1.05 - 1.10 |
| Residual Vinyl Acetate Monomer | < 0.1 |
| Freeze Thaw Stability | Stable up to 5 cycles |
| Mechanical Stability | Excellent |
| Storage Stability Months | 12 |
| Film Properties | Flexible and transparent |
As an accredited GW-706 VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | GW-706 VAE Emulsion is packaged in 200 kg drums, sealed to prevent leakage and contamination during transport. |
| Container Loading (20′ FCL) | Load GW-706 VAE Emulsion into 20′ FCL using drums/IBCs, secured properly, away from heat, with safe handling precautions. |
| Shipping | GW-706 VAE Emulsion ships in sealed drums, IBC totes, or bulk tankers. It is typically non-hazardous and non-DG, but protect from freezing, extreme heat, and contamination. Keep containers upright, dry, and well-ventilated, with proper labeling and spill containment. |
| Storage | Store GW-706 VAE Emulsion in a sealed, original container in a cool, dry, well-ventilated area. Avoid direct sunlight, excessive heat, and freezing; ideal storage temperature is 5–35°C. Keep away from oxidizers and incompatible chemicals. Stir gently before use and follow the manufacturer’s shelf-life guidelines for best performance. |
| Shelf Life | Shelf life: 6 months from manufacture when stored in original sealed containers at 5–35°C; protect from freezing. |
Paint formulators targeting a pigment volume concentration (PVC) between 72% and 82% routinely encounter a conflict between hiding power and wet-scrub integrity. GW-706, with a glass transition temperature of approximately 5 °C and a minimum film-forming temperature below 0 °C, eliminates the need for external coalescents above 12 °C application temperature. This is critical because coalescent demand in high-PVC systems destabilizes associative thickener networks. In a formulation loaded with 350 kg of TiO₂ (ISO 591-1 R2) and 120 kg of calcined kaolin per metric ton, GW-706 is typically dosed at 8–12% dry binder on total wet weight. The wet-state pH is buffered to 8.0–8.8 with ammonia or AMP-95 to maintain associative HEUR thickener efficiency; the emulsion’s native pH of 4.0–5.0 requires this adjustment before letdown. High-shear dispersion via a Cowles blade at 18–22 m/s tip speed incorporates the pigment, after which the binder is added under reduced agitation to avoid micro-foam. Scrub resistance tested per ISO 11998 on a 200 µm wet-film drawdown over Leneta P121-10N charts routinely exceeds 200 cycles before 70% film removal, provided the coalescent-free film achieves full particle deformation within 48 hours at 23 °C/50% RH. The vinyl acetate-ethylene backbone delivers inherently higher wet adhesion to alkyd-primed surfaces compared to pure acrylic emulsions in this PVC band, a property mapped by ASTM D3359-17 crosshatch after 24-hour water soak. One operational boundary is that PVC exceeding 84% generates micro-porosity sufficient to cause rapid surfactant leaching when exposed to condensation; titanium dioxide grades with dense silica coating are preferred to suppress photocatalytic binder degradation.
When the construction site demands compliance with South Coast AQMD Rule 1113 for flat coatings (50 g/L VOC maximum), GW-706 permits a zero-coalescent, zero-plasticizer formula that still passes low-temperature coalescence testing on a 5 °C substrate. The dry film does not embrittle below 10 °C, an advantage over vinyl acetate-veova copolymers that exhibit a steeper modulus increase. Process-wise, in-plant tinting with universal colorants at 60 mL/L requires that the letdown phase include a nonionic surfactant with an HLB of 13–15 at 0.3% on total liquid to prevent pigment shock, a failure mode where tint-strength drops by 15–20%. Finished products range from ceiling whites to deep-base pastels when formulated with a KU viscosity of 95–105 and an ICI cone-and-plate viscosity of 1.0–1.5 poise.
Carded-thermal or spunlace nonwovens for industrial wipes and hygiene top-sheet demand a balance between wet tensile strength and softness that saturated binder application must deliver without stiffening the web. GW-706 is spray-applied via a series of oscillating hydraulic nozzles at a line pressure of 2.5–4.0 bar onto a web travelling at 80–150 m/min, with add-on weight controlled between 8 g/m² and 22 g/m² dry. Because the emulsion is internally plasticized, the need for external plasticizers—which would migrate and increase blocking under roll compression—is eliminated. The binder bath includes a melamine-formaldehyde crosslinker at 0.5–1.2% on binder solids, and acetic acid is used to adjust the bath pH to 3.8–4.2. The crosslinking reaction proceeds in a through-air drum dryer with a dwell time of 45–70 seconds at 135–145 °C air temperature, and full cure is verified by a methyl ethyl ketone rub test per ASTM D5402 showing no surface dissolution. Wet tensile strength measured according to EDANA NWSP 110.4.R0 typically exceeds 58 N/5cm in the machine direction for a 40 g/m² substrate with 20% binder content, while cross-direction values retain at least 75% of the MD figure. This anisotropy ratio of 0.75–0.85 is a key converting spec for folding wipes dispensed from center-pull rolls.
Adhesion to polypropylene is notoriously poor; here the surface tension of the bath must be reduced below 32 mN/m using a siloxane-based superwetter at 0.2% active. Flame-pretreatment of the web raises the dyne level of PP fibers above 48 dyne/cm before binder application, a step that prevents catastrophic delamination during the wet-wipe re-wetting test. An important limitation is that drying temperatures above 155 °C cause the EVA comonomer segments to degrade and generate acetic acid odor that is unacceptable for baby wipes, making the narrow drying window a production bottleneck. Finished articles are converted into perforated rolls for food-service or industrial degreasing wipes, where the absence of alkylphenol ethoxylates (APEO-free) is mandatory under REACH Annex XVII entry 46a.
Paper cup side-seam adhesives formulated with GW-706 must meet a dual challenge: immediate green tack on clay-coated board and sustained water resistance under hot-fill conditions. A typical side-seam compound is prepared by thickening the emulsion with a 2.5% solution of carboxymethyl cellulose (DS 0.7–0.9) to reach a Brookfield viscosity of 18,000–22,000 mPa·s at 20 rpm. The high-solids content of GW-706 (54–56% nonvolatile) permits a fast set rate on the high-speed cup former running at 120–180 cups per minute. A boric acid addition of 0.8–1.5% on wet weight complexes with the polyvinyl alcohol protective colloid in the emulsion, creating a thixotropic paste that resists extrusion under the compression belts. The seam is heated by hot air at 400–450 °C for 1.2–1.8 seconds, forcing water out and forming a coalesced film that registers a fiber-tear bond in excess of 90% when tested via TAPPI T 543.
Food contact compliance is the non-negotiable driver: GW-706 meets FDA 21 CFR 176.170 (components of paper and paperboard in contact with aqueous and fatty foods) and EU Regulation 10/2011 with specific migration limits for vinyl acetate below 12 mg/kg. Migration testing is conducted per EN 1186-1 with 3% acetic acid simulant at 100 °C for 2 hours. For grease-resistant grades, a 0.5–1.0 mm bead of compounded adhesive is applied precisely by a Nordson slot-coating head, and the finished cup must pass the 30-minute hot-water-leak test where no blue-dye wicking beyond the seam is permitted. The remoistenability of the dried film is poor, so this formulation is unsuitable for envelope window adhesives where rewetting is required.
| Standard / Regulation | Test Condition | Typical Result | Required Limit |
|---|---|---|---|
| FDA 21 CFR 176.170 | Distilled water, 120 °F, 24 h | <2 mg/dm² extractives | No specific numeric limit; good manufacturing practice |
| EU 10/2011 (overall migration) | 3% acetic acid, 100 °C, 2 h | 6–9 mg/dm² | 10 mg/dm² |
| BfR Recommendation XXXVI | 60 °C water, 24 h | 0.8–1.4 mg/dm² | 5 mg/dm² |
| EN 13432 (biodegradability in composting) | 28-day aerobic test | >90% relative to microcrystalline cellulose | >90% absolute or relative |
The above values derive from industrial campaign data when GW-706 is used as the sole binder without extraneous plasticizers. The acetic acid migration figure is sensitive to residual acetate ion; a post-polymerization stripping step at the production plant controls free vinyl acetate monomer below 500 ppm, which is a critical batch-release parameter.
GW-706 compounded with calcium carbonate filler at a 100:80 to 100:120 dry ratio forms the base of a precoat paste applied through a slot die onto the back of tufted nylon carpet. The flow must remain Newtonian enough to penetrate the primary backing yet build a yield value that prevents strike-through to the face fiber. Typically, a polyacrylic acid alkali-swellable thickener is added at 0.3–0.7% active, targeting a Brookfield RVT spindle #6 viscosity of 25,000–30,000 mPa·s. Over the course of a production shift, the heat generated by the circulation pump and the mechanical work of the in-line disperser can cause a viscosity increase of 10–15%, especially if the filler is a ground calcium carbonate with a steep particle size distribution. This viscosity drift forces the operator to make incremental dilution water additions, which in turn reduces dry add-on and correlates with a tuft bind loss of 0.5–1.2 kg in anchorage force per tuft. The countermeasure is to pre-cool the make-up water to 10–12 °C and install a jacket on the holding tank, maintaining the compound at 28 °C maximum.
Tuft bind is measured per ASTM D1335, and values above 4.5 kg for a 1/10-gauge cut-pile nylon are achieved with a precoat dry add-on of 22–28 oz/yd². After precoat drying in a three-zone gas-fired impingement oven at 160 °C, a secondary high-filler PB latex compound is applied and the carpet cured. GW-706 contributes flexibility at the hinge of the tile, critical during the 60-day flat-lay test where a tile must not curl more than 2.5 mm per 45 cm edge when tested to ISO 24343-1. The residual tack of the emulsion film after oven exit, if not fully de-tackified by filler loading, can cause blocking in stacks of uncut rolls; a talc dusting at 5–8 g/m² is a palliative rather than a cure, reflecting a limitation of internally plasticized VAE chemistry in this specific heavy-fill application.
Edge-gluing of beech or oak parquet strips uses a one-part polyvinyl acetate adhesive fortified with GW-706 at a 5–15% replacement level for homopolymer PVAc. The purpose is to meet the EN 204 D3 durability class (interior with frequent short-term water exposure) without the toxicity labeling burden of monomeric isocyanates. The blend is thickened with polyvinyl alcohol (DK-value 80–88% hydrolysis, 4% solution viscosity 20–25 mPa·s) to a final viscosity of 10,000–14,000 mPa·s, and contains 3–5% propylene carbonate as a fugitive plasticizer. Assembly time on a radio-frequency glue press is 6–8 minutes under 0.7–1.0 N/mm² compression. The water-resistance test involves storing the bonded specimen in water at 20 °C for 4 days and then testing tensile shear strength per EN 205; a minimum of 2 N/mm² is required for D3. With a 70:30 PVAc homopolymer-to-GW-706 blend, shear values typically fall in the range 2.6–3.2 N/mm², compared to 1.8–2.1 N/mm² for the pure homopolymer.
The limitation is that D4 classification (boiling water immersion) cannot be reached with this system in the absence of crosslinkers; bondline creep at 60 °C under DIN EN 14257 also degrades if the GW-706 fraction exceeds 25%, because the ethylene segments soften the matrix. Hardwood flooring installers recognize the cured film’s slight thermoplasticity when sanding at belt speeds above 300 m/min; clogging of P80 grit belts is reported if the glue line is not allowed to fully cool between passes. The final product is a D2/D3 wood flooring adhesive sold in 14 kg pails for the professional installer, combining low formaldehyde emission (ISO 16000-3, <0.03 ppm after 28 days) with a working life exceeding 60 minutes at 23 °C.
GW-706 is incorporated into two-component cementitious flexible waterproofing slurries at a polymer-to-cement ratio (p/c) of 0.25–0.40 by weight. The liquid component blends the emulsion with a plasticizer, a defoamer based on mineral oil (0.5%), and a polycarboxylate superplasticizer at 0.8% on cement to maintain a flow diameter of 140–160 mm per GB/T 23445-2009. The dry component mixes ordinary Portland cement CEM I 42.5R with 40–60% silica sand 0.1–0.5 mm. After trowel application to a concrete substrate at 1.5–2.0 kg/m² per coat, the film cures through hydraulic setting and polymer coalescence. Crack-bridging ability at –10 °C on a 2 mm dried film exceeds 0.75 mm static opening before rupture, determined by EN 1062-7 method A. The key adhesion test is pull-off strength on a prematurely dried, absorbent concrete block (8% moisture content), where values above 0.8 N/mm² after 7 days wet conditioning and 7 days dry storage are expected. The highly alkaline pore solution attacks native vinyl acetate polymers; the ethylene unit in GW-706 imparts saponification resistance that extends functional service life, yet prolonged exposure to constant water head at pH above 12.5 will eventually hydrolyze the polymer film, reducing elongation at break to less than 50% after 90 days of continuous immersion per accelerated durability protocols. For roof terraces exposed to permanent hydrostatic pressure, an epoxy primer is recommended before the VAE-modified cementitious membrane is applied. Produced articles are two-part kits in plastic buckets, consumed on-site within 1 hour after mixing due to a pot life governed by initial cement set.
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| Property | Test Method | GW-706 VAE | Conventional High-Ethylene VAE | Styrene-Acrylic Dispersion (Tg −10 °C) |
|---|---|---|---|---|
| Solids content (%) | ISO 3251 | 55.0 ± 1.0 | 54.5 ± 1.0 | 50.0 ± 1.0 |
| Viscosity (mPa·s, Brookfield RVT, spindle 4, 20 rpm) | ISO 2555 | 2800–3500 | 2200–3000 | 800–1500 |
| MFFT (°C) | ISO 2115 | 0 | 2 | 12 |
| Tensile strength (MPa) | ISO 527-3 | 8.1 | 5.4 | 9.7 |
| Elongation at break (%) | ISO 527-3 | 680 | 780 | 410 |
| 180° peel adhesion on PE (N/mm) | ASTM D3330 | 1.8 | 0.9 | 0.3 |
| Heat resistance temperature (°C, SAFT, 1 kg) | ASTM D4498 | 112 | 88 | 131 |