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Anhui Liwei Chemical Co., Limited.

GW-102H High-Ethylene VAE Emulsion

    • Product Name: GW-102H High-Ethylene VAE Emulsion
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
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    Specifications
    HS Code 732891
    Product Type High-Ethylene Vinyl Acetate-Ethylene (VAE) Copolymer Emulsion
    Appearance White milky liquid
    Solid Content 55.0 ± 1.0 wt%
    Viscosity 2000 - 4000 mPa·s (Brookfield, 25°C)
    Ph 4.5 - 5.5
    Density 1.05 - 1.10 g/cm³ at 25°C
    Particle Size 0.5 - 2.0 μm
    Glass Transition Temperature -20°C to -15°C
    Minimum Film Forming Temperature ≤ 0°C
    Ethylene Content 25 - 35 wt%
    Film Tensile Strength ≥ 5 MPa
    Film Elongation At Break ≥ 600%
    Residual Vinyl Acetate Monomer ≤ 0.1 wt%

    As an accredited GW-102H High-Ethylene VAE Emulsion factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in sealed 200 kg drums or 1000 kg IBC totes, ensuring safe storage and handling of GW-102H VAE emulsion.
    Container Loading (20′ FCL) GW-102H High-Ethylene VAE Emulsion container loaded in 20-foot FCL. Secure drums/pails, protect from freezing, ensure proper ventilation for safe transport.
    Shipping GW-102H High-Ethylene VAE Emulsion is shipped in sealed drums or IBC totes to prevent leakage. Store away from extreme heat and freezing temperatures; keep containers upright and protected from damage. Refer to SDS for handling and disposal guidelines.
    Storage Store GW-102H High-Ethylene VAE Emulsion in sealed, original containers in a cool, dry, well-ventilated area away from direct sunlight and heat sources. Maintain temperatures between 5°C and 35°C; do not allow freezing. Keep containers tightly closed to prevent skinning or contamination. Stir gently before use and adhere to shelf life guidelines.
    Shelf Life Shelf life is typically 12 months from manufacture when stored sealed in a cool, dry place, protected from freezing.
    Application of GW-102H High-Ethylene VAE Emulsion

    Three-roll random fiber carding lines delivering a 12–18 g/m² PE/PP bicomponent web at line speeds exceeding 300 m/min have exposed the limitations of standard VAE binders in maintaining wet integrity. On a Reicofil-type spunbond line running a 15 g/m² pure polypropylene sheet, the contact angle of a surfactant-stabilized VAE with a Tg above 0 °C typically falls below 70° on the untreated PP layer, leading to strikethrough and bond failure in the cross-direction after saline exposure per WSP 401.0. GW-102H, with a high-ethylene content pushing its Tg into the -15 °C to -5 °C window and a surface energy below 35 mN/m, eliminates the need for a separate wetting package in most polyolefin-based nonwoven assemblies. The binder is applied via a slot-die coating station or a parabolic foam applicator, typically using a pre-foamed dispersion at 30–35 % solids and a blow ratio of 1:4 to 1:6 on a Hansa Mixer A 600. Penetration is governed by the vacuum box setting on the forming wire: a negative pressure of 0.4–0.8 kPa prevents adhesive strike-through into the backside release liner while achieving an add-on of 2.5–4.0 g/m² dry weight. Compliance for hygiene end uses follows ISO 10993-10:2021 for skin sensitization, OEKO-TEX Standard 100 class I, and the broader chemical restrictions of EU 10/2011 when a polyolefin backsheet is considered an indirect food-contact barrier. The formulation is supplied as a single-package system; manufacturers adding a colloidal silica anti-block agent, such as 1.0–1.5 wt% Lehvoss N 20, must pre-disperse it in a separate water phase to avoid shear-induced coagulation when the emulsion pH drops below 4.0 in the circulation loop. Finished articles range from baby diaper leg cuffs and acquisition‑distribution layers to adult incontinence briefe's waistband elastics, where the elastic modulus of the cured adhesive at 38 °C must remain below 0.3 MPa to prevent pressure marks under occlusive plastic pants.

    What Prevents Delamination in Low-Surface-Energy Film Laminates After Hot-Fill Processing?

    In dry‑bond laminating of biaxially oriented polypropylene (BOPP) to cast polypropylene (CPP) for retort pouches, the absence of polar functionality on either substrate forces formulators to rely on surface pretreatment levels that degrade over time. A corona-treated BOPP film with an initial dyne level of 42 mN/m can drop to 36 mN/m within 72 hours in a warehouse with 60 % RH. GW-102H at 50 % solids and blended with a pentaerythritol ester of rosin (softening point 85 °C) at a ratio of 100:15 by dry weight provides a green tack exceeding 4 N/25 mm on 38 mN/m CPP when tested according to ASTM D3330/D3330M-04 method A. The adhesive mass is gravure-printed onto the primary web at a coat weight of 1.8–2.5 g/m² dry on a Nordmeccanica Super Combi 3000 laminator with a 140-line mechanically engraved cylinder. Dwell time in the drying tunnel above 70 °C must not exceed 2.5 seconds; longer residence causes the polyethylene-rich domains of the emulsion film to coalesce prematurely, trapping moisture that later delaminates the bond when the pouch is filled at 85–90 °C. Compliance is verified under FDA 21 CFR 175.105 and the specific migration limits of EU Regulation 10/2011 annex II for fatty food simulant D2. Production batches must be agitated with a slow-speed anchor mixer rather than a high-shear disperser, because air entrainment above 0.5 % by volume creates pinhole defects visible under a 20× magnifier. Finished structures include stand-up pouches for liquid detergent refills and microwavable rice packs, where seal-strength values above 20 N/15 mm are achieved only when the laminated roll is conditioned at 40 °C for 48 hours prior to slitting.

    Waterproofing Membrane Crack-Bridging at -10 °C

    Polymer‑modified cementitious waterproofing slurries that must meet the 0.75 mm crack-bridging requirement of EN 14891:2017 at -10 °C face a fundamental rheological conflict: the cement hydration rate demands a water-to-cement ratio above 0.40, yet free water reduces the polymer volume fraction and shifts the film-forming temperature upward. A formulation combining 100 parts by weight of an Ordinary Portland Cement CEM I 42.5 R with 55–65 parts of GW-102H (55 % solids) and 0.3 parts of a polycarboxylate superplasticizer delivers a stiff trowel-grade consistency with an initial slump of 110 mm on a flow table. When the polymer-to-cement ratio (p/c) reaches 0.18–0.22, the interpenetrating co-matrix of hydrates and coalesced VAE domains achieves an elongation at break above 200 % at -10 °C as measured by ISO 527-3:2018 on free films cast and cured for 7 days at 90 % RH followed by 21 days at 50 % RH. Two-component mixing on site employs a slow-speed paddle (300 rpm) to avoid air entrainment that reduces tensile adhesion strength below the 0.5 MPa minimum mandated by EN 1542 for concrete floor slabs. The workable pot life at 23 °C drops sharply from 60 minutes to 20 minutes when the substrate temperature exceeds 35 °C due to accelerated film-formation at the evaporative surface; re-tempering with water is prohibited because it disrupts the p/c balance and induces micro-cracking visible under scanning electron microscopy. Typical end products include below-grade external basement tanking systems, tiled balcony membranes, and liquid-applied flashing for roof penetration details. Direct exposure to UV radiation longer than 6 months without a protective screed or tile layer is not recommended, as the ethylene segments undergo slow photo-oxidative chain scission that reduces low-temperature flexibility.

    Calendering of debossed PVC plastisol-free floor covering has exposed the migration‑rate dependency on the polymeric plasticizer choice. When a 0.15 mm compact layer of GW-102H is applied between a glass-fibre fleece backing and a decorative print film by means of a knife-over-roller coater, the residual moisture content at the exit of the 12-metre convection oven must be held below 0.8 % to prevent steam blistering during subsequent hot‑press lamination at 180 °C under 4 bar line pressure. The emulsion is used at neat solids without dilution, deposition being controlled by the gap height set at 0.20–0.25 mm on a Mathis LTE-S coater. While conventional VAE with a vinyl acetate content above 85 % turns yellow within 30 minutes under the 180 °C regime, the high-ethylene backbone of GW-102H resists thermal discolouration up to 45 minutes of dwell time, confirmed by a delta E value below 3.0 measured via spectrophotometer against a baked white tile standard. Formulators referencing EN 14041:2018 for indoor floor coverings must verify the TVOC emission after 3 days in a chamber test per EN 16516, typically achieving values below 0.25 mg/m³ when no coalescing solvent is added. A documented incompatibility arises with residual amine-functional silane adhesion promoters in the glass fleece; if the fleece supplier uses an aminopropyltriethoxysilane finish, the acidic pH of GW-102H (4.5–5.0) protonates the amine and creates a tacky, moisture-sensitive interphase that reduces peel strength by more than 30 % after 24-hour water immersion per DIN EN 1372. Facilities running continuous lines with an accumulator must set the turret winder tension to 40–50 N for 1.5-metre roll widths to avoid telescoping, since the hot film possesses minimal hot-block resistance until cooled below 35 °C.

    When Paper-Based Packaging Requires Repulpability Without Sacrificing MVTR

    The switch from extrusion-coated LDPE to aqueous barrier coatings on cupstock board has placed a dual demand on the binder: a moisture vapor transmission rate (MVTR) below 150 g/m²·24 h at 38 °C and 90 % RH when applied at 10–12 g/m² dry, and a repulping screen reject below 1.5 % under TAPPI/ANSI UM 213. GW-102H formulated with a plate-like talc additive (8 wt% on dry binder) and coated on a Valmet OptiCoat Layer curtain coater at 800 m/min achieves an MVTR of 135 g/m²·24 h without requiring a secondary drying stage. The curtain impingement velocity is set to 2.5 m/s to prevent air-bubble rupture across the 3.2-metre die width. Because the emulsion particle size distribution is centred on 0.6 μm, the coating penetrates less than 15 μm into a 280 g/m² solid bleached sulphate board, preserving bulk and stiffness while achieving a Cobb60 value below 2.5 g/m² as tested per ISO 535:2023. Compliance for food contact is governed by FDA 21 CFR 176.170 and 176.180, the German BfR Recommendation XIV, and the overall migration limit of 10 mg/dm² in EU 10/2011. Any modification with an external crosslinker such as ammonium zirconium carbonate must stay below 0.3 % by weight to avoid forming a thermoset network that blocks the pulper rotor and increases energy consumption beyond 50 kWh/ton of recovered fibre. Finished articles include hot-beverage takeaway cups, ice-cream tubs, and paperboard soup bowls with a liquid holdout exceeding 2 hours at 80 °C. Mills operating a Voith EcoCell pulper must wash the coating off at 45 °C and pH 8; attempts to repulp in cold water at neutral pH result in macro-stickies that blind the 0.15 mm slotted screen within 20 minutes of batch circulation.

    High-Filler-Loaded Precoat Applications and the Viscosity Creep Phenomenon

    A tufted carpet precoat compound carrying 600 phr of ground calcium carbonate (D50 = 5 μm) requires a binder that retains a Brookfield RVT viscosity below 12,000 mPa·s when measured at 23 °C with a #6 spindle at 20 rpm after 24 hours of low-shear ageing. GW-102H filled at the 600 phr level with an Omyacarb 5-GU filler and 0.5% sodium polyacrylate dispersant exhibits an initial viscosity of 9,800 mPa·s and a creep of less than 8 % over 48 hours, significantly below the plateau seen with conventional vinyl acetate homopolymer emulsions that typically rise to 25,000 mPa·s due to alkali-swellable thickener interaction with calcium ions. The compound is foamed on a Cowie & Riding Gen 4 mechanical foamer to a density of 250–350 g/L and spread via a knife-over-blanket applicator onto a primary backing of woven polypropylene. Wet pick-up on a 28 oz/yd² carpet is controlled to 3.5 oz/yd² dry precoat weight. Gelation in the latex-filler matrix at the pin-curing oven entry must occur within 90 seconds at 130 °C wet-bulb temperature; GW-102H’s rapid skin-forming characteristic prevents strike-through into the face yarn, preserving tip definition. The relevant fire-safety benchmark is the methenamine pill test under ASTM D2859-21, while the adhesive bond between the precoat and the secondary backing is judged by the anchorage test of ASTM D1335-21, with a minimum 3.5 kg pull required per tuft row. A processing limitation manifests when the carpet line stops for more than 15 minutes: the precoat left in the foam transfer hose begins to seed, and restarting flow breaks these seeds into visible hard spots in the coating. Only an air-purged bypass loop with a 2-bar back-pressure valve prevents accumulation. End products are broadloom contract carpets and modular carpet tiles supplied to the hospitality sector, where the total VOC emission after 24 hours must remain under the GUT/Mutas limit of 0.25 mg/m³ TVOC in a chamber test.

    Anti-blocking Properties in Stretch Textile Screen Prints Exposed to Stacked Curing

    Rotary screen-printed logos on 180 g/m² cotton-Lycra® jersey demand a water-based ink binder that does not fuse inter-layer at 45 °C under 5 kPa stack pressure inside a curing trolley. GW-102H forms a discrete film with a König pendulum hardness of 30–40 oscillations (ISO 1522:2022) when dried without external crosslinker, yet when a trifunctional aziridine curative such as XAMA-7 is added at 1.2–1.8 wt% on total binder solids, the film develops a gel content above 92 % by methyl ethyl ketone extraction and withstands 40 wash cycles at 60 °C under ISO 6330:2012 procedure 6A without surface pilling. The print paste is prepared at 97 % binder solids content, mixed with 3 % high-strength fumed silica for thixotropy, and printed through a 125 mesh screen at a squeegee angle of 15°. Curing is executed in a gas-fired tunnel dryer with a 3-minute dwell at 150 °C fabric surface temperature as measured by an optical pyrometer. The formulation is routinely audited against the ZDHC Level 3 requirements of the Zero Discharge of Hazardous Chemicals programme and must pass OEKO-TEX Standard 100 Class II for skin-contact garments. An interaction with cationic silicone softeners applied during garment wash post-printing has been documented: the softener deposits on the film surface and lifts the inter-coat adhesion when the garment is tumble-dried at 80 °C, causing delamination after 3–5 industrial laundry cycles. The recommended sequence is to apply the silicone softener in the rinse bath before printing, not after. Final garment placements include athletic-wear numbering, fashion-label tags, and heat-transferred patches where the film must not crack when the fabric is extended to 25 % elongation on a tensile tester set to 300 mm/min crosshead speed.

    Application-to-Standard Compliance Matrix for GW-102H
    ScenarioDominant Regulatory StandardsTypical Application Rate (dry g/m² or phr)Critical Performance Metric
    Nonwoven hygiene adhesiveISO 10993-10:2021, OEKO-TEX 100 I, EU 10/20112.5–4.0 g/m²Wet bond strength after saline, WSP 401.0
    Flexible packaging laminationFDA 21 CFR 175.105, EU 10/20111.8–2.5 g/m²Hot-fill peel > 4 N/25 mm
    Cementitious waterproofingEN 14891:2017, EN 1542p/c = 0.18–0.22Crack bridging 0.75 mm at -10 °C
    PVC-free flooring interlayerEN 14041:2018, EN 16516Neat, 0.15 mm compact layerDelta E < 3.0 after 45 min at 180 °C
    Paperboard barrier coatingFDA 21 CFR 176.170/180, BfR XIV, EU 10/2011, TAPPI UM 21310–12 g/m²MVTR < 150 g/m²·24 h, repulp reject < 1.5 %
    Carpet precoatASTM D2859-21, ASTM D1335-21, GUT/Mutas600 phr CaCO₃, 3.5 oz/yd²Viscosity creep < 8 % over 48 h
    Textile screen printingOEKO-TEX Standard 100 II, ZDHC Level 3, ISO 6330:20121.2–1.8 wt% aziridine on binder solidsGel content > 92 %, no inter-layer blocking
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    Certification & Compliance
    More Introduction
    The GW-102H designation identifies an aqueous vinyl acetate-ethylene copolymer emulsion in which the ethylene comonomer fraction exceeds 25 wt% on dry substance, producing a semi-crystalline, permanently flexible film without the use of external phthalate or adipate plasticizers. Primary specification data, determined in accordance with ISO 3251 (gravimetric solids, 1 h at 105 °C), ISO 976 (pH), and ASTM D2196/ISO 2555 (Brookfield RV viscosity, spindle #3, 20 rpm, 25 °C), are: solids content 54–56%, viscosity 500–3,000 mPa·s, and pH 4.5–5.5. The minimum film-forming temperature (MFFT) recorded on a Rhopoint gradient bar per ISO 2115 is 0 °C, while the dried copolymer displays a glass transition midpoint of approximately -15 °C by differential scanning calorimetry (ISO 11357-2, 10 K/min). This high-ethylene architecture distinguishes GW-102H from low- and medium-ethylene VAE grades (ethylene 10–18%) and from poly(vinyl acetate) homopolymers, whose films require coalescing solvents or fugitive plasticizers to approach similar low-temperature flexibility and which absorb significantly more water under identical exposure: typical water uptake after 24 h immersion (ISO 62) falls to 3–5%, compared with 20–25% for homopolymer and 10–12% for a 16%-ethylene VAE. The intrinsic hydrophobicity also retards alkaline hydrolysis, making the emulsion inherently more stable in cementitious environments and enabling formulations that meet the REACH Annex XVII restriction on phthalates without post-cure remediation. A full-scale 3-layer pouch laminator running a tandem extrusion lamination line with an in-line slot-die aqueous coater was evaluated at 150 m/min using GW-102H applied at 2.0 g/m² (dry) onto 20 µm corona-treated LDPE (42 dyne/cm). Film coalescence occurred without heated carrier rolls because the MFFT of 0 °C was below ambient-on-web temperature, yet the emulsion required a dynamic surface tension below 35 mN/m (measured via ASTM D3825 bubble pressure at 10 Hz) to avoid retraction on the low-energy surface; a 2-ethylhexyl sulfate anionic wetting aid was pre-dispersed at 0.3 wt% on wet emulsion. T-peel adhesion after secondary heat lamination to 12 µm metallized PET and 48 h conditioning at 23 °C/50% RH reached 2.8–3.2 N/15 mm (ASTM D1876-08) with cohesive failure within the VAE layer observed in 85% of bonded area. When 10 wt% of a rosin ester dispersion (softening point 85 °C) was incorporated to raise adhesion to non-corona PE, the blend MFFT rose to 5–8 °C, requiring substrate pre-heating to 30 °C via an IR panel (60 °C emitter, dwell 3 s) to maintain film integrity; failure to pre-heat resulted in micro-crazing of the dry film and a peel strength drop to 1.0 N/15 mm. No tackifier addition is necessary for standard corona-treated PE, preserving a single-component system with a pot life exceeding 72 h in a closed recirculation loop monitored by a Marimex flow-through viscometer.
    PropertyGW-102H (High-Et)GW-105 (Medium-Et VAE)PVAc Homopolymer
    Ethylene content (wt% on dry)>2514–160
    Solids (ISO 3251)54–56%54–56%50–52%
    Viscosity (Brookfield RV #3/20 rpm)500–3,000 mPa·s1,500–4,000 mPa·s8,000–20,000 mPa·s
    MFFT (ISO 2115)0 °C5–6 °C16–18 °C
    Tg DSC midpoint (ISO 11357-2)-15 °C+5 °C+32 °C
    Water absorption (24 h, ISO 62)3–5%10–12%20–25%
    Elongation at break (ISO 37 Type 2)>600%300–400%<20% (brittle)
    Coalescing solvent demand (on wet)none at 0 °C film formation2–4% butyl glycol6–10% texanol

    What Makes High-Ethylene VAE Emulsion Superior for Low-Surface-Energy Substrates?

    The ethylene-rich backbone reduces overall cohesive energy density, enabling wetting on untreated polypropylene (30 dyne/cm) when the emulsion is applied with a dynamic contact angle below 60° at 0.1 s drop age; a Krüss BP100 tensiometer confirmed equilibrium surface tension of 42 mN/m at 10 Hz. In contrast, a medium-ethylene VAE with a film Tg of +5 °C requires a coalescent that lowers interfacial tension but also softens the dried film, reducing heat resistance in downstream lamination to PET. GW-102H maintains a softening point above 120 °C (Kofler hot bench) while wetting automatically, thus meeting the FDA 21 CFR 175.105 and 176.170 indirect food-contact requirements for laminated structures without migration of low-molecular-weight plasticizer.

    Carpet Pre-Coat Rheology and Plasticizer-Free Tuft-Bind Compliance

    A pre-coat compound for a 900 g/m² loop-pile nylon carpet was formulated on a Ross VMC-40 vacuum mixer: 100 parts GW-102H wet, 200 parts Omyacarb 5 µm CaCO₃, 0.2 parts associative polyurethane thickener (Borchi Gel 0620). Brookfield RV viscosity at 50 rpm was adjusted to 12,000 mPa·s for knife-over-roll application at 2.5 mm gap; the thickened system showed Newtonian plateau behavior up to 500 s⁻¹, preventing striations during doctoring. Tuft bind measured per ASTM D1335 on the latex-backed carpet after 24 h conditioning was 5.8–6.5 kg. After 7 days at 70 °C in a forced-air oven simulating automotive interior aging, retention exceeded 72% (4.5 kg), with no plasticizer volatilization. This compares with a conventional PVAc/DBP system where tuft bind drops below 2.5 kg under identical aging, failing IMO FTP Code Part 2 fire-retardant integrity due to plasticizer migration into the face fiber. GW-102H is manufactured with a protective-colloid (polyvinyl alcohol) stabilization regime rather than a high-surfactant profile; extractable surfactant residue is below 0.5% by ISO 787-11 hot toluene extraction, drastically reducing the risk of staining on vinyl flooring exposed to underfloor heating, as verified by ISO 105-B02 xenon arc lightfastness testing (blue wool ≥6). Because the ethylene segments interrupt the regularity of the acetate blocks, amorphous domains dominate even after mechanical drawing. A 500 µm cast film of GW-102H subjected to 100% elongation at 300 mm/min (ISO 527-3) retains transparency (haze <5% per ASTM D1003) and does not stress-whiten, unlike EVA copolymers with higher vinyl acetate. This feature is exploited in window film adhesive and laminated safety glass interlayers where optical clarity is critical. The absence of coalescent also eliminates VOC emission above 0.1 mg/m³ after 28 days in a 1 m³ chamber (ISO 16000-6), qualifying the raw emulsion for Blue Angel RAL-UZ 113 certified low-emission floor adhesives. In cementitious two-component waterproofing slurry (polymer-to-cement ratio 0.13, Type I 42.5 R Portland cement, w/c = 0.35), GW-102H provides a crack-bridging ability exceeding 0.75 mm at -10 °C (tested per EN 14891 procedure A.5) without the addition of an acrylic superplasticizer. Open time of the mixed slurry remains workable for 55–65 min at 20 °C as monitored by a penetrometer cone drop, but high-alumina cements must be avoided because the increased calcium aluminate content accelerates emulsion destabilization, causing aggregate syneresis within 15 min. Adhesion after 28 days of water immersion ( EN 14891, concrete substrate) averages 0.65 MPa—a value that surpasses the 0.5 MPa threshold—with failure located in the concrete rather than the polymer film. The high ethylene content also reduces the saponifiable acetate density; when cured film is immersed in 1 M NaOH at 50 °C for 14 days, weight loss is limited to 6–8% compared with 30–35% for a low-ethylene VAE, confirming long-term alkaline durability required for external tanking.

    When GW-102H Replaces Acrylic Latex in Cementitious Waterproofing

    Although styrene-acrylic dispersions are traditionally chosen for their hydrolysis resistance, the GW-102H high-ethylene variant eliminates the need for coalescing butyl dioxitol entirely, reducing lacquer-like odors during confined-space application. Compressive strength development of the modified mortar at 7 days (EN 196-1) attains 38 MPa, close to the unmodified control (42 MPa), whereas a film-forming acrylic latex at the same polymer load depresses early strength to 28 MPa. The differential arises because ethylene-rich VAE does not excessively retard cement hydration, as verified by isothermal conduction calorimetry at 20 °C showing a main silicate peak at 8.2 h versus 9.0 h for the acrylic, reflecting a more open, less-barrier film around anhydrous grains.

    Heat Resistance and Open-Time Conflicts in D4 Wood Adhesive Applications

    For high-pressure laminate (HPL) bonding to 16 mm MDF panels in a hot press at 90 °C platen temperature, GW-102H was blended with 5% polymeric MDI (Desmodur VK 10) as crosslinker to meet DIN EN 204 D4 durability classification. Creep resistance tested per EN 14256 at 80 °C and 6.5 MPa sustained 24 h without measurable slip, exceeding the BS 14256 requirement. However, the crosslinking reaction shortens the pot life substantially: viscosity monitored by a Brookfield RV at 25 °C rose from an initial 7,000 mPa·s to 15,000 mPa·s within 90 min and reached 45,000 mPa·s after 180 min, forcing a working window of less than 2 h in a non-cooled tote. Production-scale experience on a Buerkle HPL press line dictates that the mixed adhesive be held in a water-jacketed vessel at 15 °C to extend pot life to 3.5 h and that roller coater gaps be widened by 0.1 mm to accommodate the viscosity progression. A non-crosslinked GW-102H bond yields a 72 h gap-filling adhesion on HPL of 2.8 N/mm² dry (shear block, ISO 6238), but fails the D4 boil test due to adhesive hydrolysis; therefore, selective crosslinking is inherently required when end-use classification demands bonded joints resisting boiling water for 6 h.
    Regulation / StandardStatus or Test MethodRelevant Property
    REACH Annex XVIINo phthalate plasticizers; compliantIntrinsic flexibility
    FDA 21 CFR 175.105Adhesive use in indirect food contactDried film extractives <1%
    FDA 21 CFR 176.170Paper and paperboard componentsPasses extraction cell tests
    EU 10/2011Migration limit for vinyl acetate monomer <10 mg/kgResidual monomer <50 ppm
    RoHS 2011/65/EUNot intentional addition of Pb, Hg, Cd, Cr⁶⁺, PBB, PBDEICP-OES screen (EN 62321)
    Blue Angel RAL-UZ 113VOC <0.1 mg/m³ after 28 dISO 16000-6 chamber test
    ASTM D4236Chronic health hazard labeling exemptionNo toxic solvents
    During adhesive removal and cleaning, GW-102H uncrosslinked films dissolve in 30% isopropanol/water within 15 min at 40 °C, enabling press roll maintenance without chlorinated solvents; crosslinked films require a dimethyl adipate-based stripper at 50 °C for 30 min, as is practical for industrial wipe-down.