Products

Products

Anhui Liwei Chemical Co., Limited.

GW-706 VAE Emulsion

    • Product Name: GW-706 VAE Emulsion
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
    • CONTACT NOW
    Specifications
    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 & Storage
    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.
    Application of GW-706 VAE Emulsion

    What Determines Scrub Resistance in High-PVC Interior Matte Paints When the Film Must Survive ISO 11998 Class 2?

    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.

    Nonwoven Wipe Converters Targeting a CDW/Wet Cross-Direction Tensile Ratio Above 0.75

    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.

    When the Seam of a Paper Cup Must Hold Boiling Water for 30 Minutes Without Delamination

    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.

    Compliance matrix for GW-706 in paper converting (selected target parameters)
    Standard / RegulationTest ConditionTypical ResultRequired Limit
    FDA 21 CFR 176.170Distilled water, 120 °F, 24 h<2 mg/dm² extractivesNo specific numeric limit; good manufacturing practice
    EU 10/2011 (overall migration)3% acetic acid, 100 °C, 2 h6–9 mg/dm²10 mg/dm²
    BfR Recommendation XXXVI60 °C water, 24 h0.8–1.4 mg/dm²5 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.

    Tile Carpet Precoat Viscosity Drift in Continuous Slot-Die Application Over a 12-Hour Shift

    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.

    How a D2/D3 Wood Flooring Adhesive Formulation Gains Water Resistance Without Isocyanate Crosslinking

    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.

    Free Quote

    Competitive GW-706 VAE Emulsion prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615380400285 or mail to sales2@liwei-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@liwei-chem.com

    Inquiry

    Get Free Quote of Anhui Liwei Chemical Co., Limited.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction
    In emulsion polymerization, the deliberate manipulation of the ethylene-vinyl acetate ratio and the selection of a carboxyl-functional comonomer generate a dispersion class that bypasses the cohesive strength ceiling of standard homopolymeric PVAc while avoiding the plasticizer migration endemic to externally plasticized systems. GW-706 VAE Emulsion is a carboxylated vinyl acetate-ethylene copolymer dispersion stabilized with a poly(vinyl alcohol) (PVOH) protective colloid system, yielding a shear-stable, co-solvent-free aqueous binder with a solids content of 54.0–56.0 %, a residual monomer level below 500 ppm, and a minimum film formation temperature (MFFT) of 0 °C. Its primary differentiation from conventional high-ethylene VAE grades resides in the controlled grafting density of the protective colloid to the particle surface, which rebalances open time and wet tack on low-energy polymer films without the introduction of migratory tackifiers.

    Polymer Architecture and Core-Shell Morphology

    Particle architecture in GW-706 is not a homogeneous random copolymer but a gradient morphology with an ethylene-rich core and a vinyl acetate-dominant shell, confirmed by transmission electron microscopy with selective heavy-metal staining. The core contains 18–20 wt% ethylene, reducing the unplasticized glass transition temperature (Tg) to approximately −12 °C by differential scanning calorimetry at a heating rate of 10 K/min. The shell phase carries the carboxyl functionality, introduced via 1.5–2.5 wt% of acrylic acid or maleic anhydride equivalent, providing reactive sites for subsequent ionic or covalent crosslinking. Particle size distribution, measured by dynamic light scattering (ISO 22412:2017), exhibits a D50 of 0.65 µm and a span of 1.0, indicative of a moderately broad distribution favorable for high-shear stability in roll-coating equipment. The PVOH grafting efficiency, quantified via Soxhlet extraction and iodine complexation, exceeds 60 %, which accounts for the pronounced shear-thinning behavior observed on a cone-and-plate rheometer at shear rates above 500 s⁻¹.

    What Limits the Adhesion Spectrum on Polyolefin Substrates?

    Performance on low-surface-energy substrates such as untreated polypropylene (surface energy 28–30 mN/m) is not dictated solely by the ethylene content of the copolymer but by the interfacial chain mobility during film coalescence. In GW-706, the core-shell morphology delays the interdiffusion of the ethylene-rich segments until the later stages of drying, allowing the polar vinyl acetate shell to first wet the substrate. Lap shear adhesion on corona-treated polypropylene film, tested per ASTM D3163-01 with a bondline thickness of 150 µm, reaches 4.2 MPa after 7-day ambient cure, a value roughly 30 % higher than that of a conventional high-ethylene VAE of equivalent bulk ethylene content but lacking the core-shell gradient. On untreated polyethylene, the failure mode remains adhesion failure; however, the incorporation of 2 phr of a silane adhesion promoter (e.g., gamma-glycidoxypropyltrimethoxysilane) into the compounded formulation shifts the peel force from 0.8 N/mm to 2.1 N/mm, measured at a 180° angle and 300 mm/min crosshead speed. Published data for performance on untreated PTFE remains limited. In high-speed lamination of PVC decorative foils to MDF panels, GW-706 replaces two-component polyurethane dispersions where the curing time of 48–72 hours imposes a throughput bottleneck. The emulsion is applied via a ribbed roller at a coat weight of 35–45 g/m² wet. Initial tack, measured by a probe tack tester (ASTM D2979-16), exceeds 8 N within 20 seconds of contact, allowing immediate stacking of laminated boards without a drying tunnel. The high PVOH content of the protective colloid, typically 4–6 wt% based on polymer solids, contributes to the rapid development of green strength but also limits water resistance unless chemically insolubilized. When post-crosslinked with 1.5 wt% glyoxal (on emulsion weight), the laminated assembly withstands a 24-hour water immersion at 23 °C without blistering or edge delamination, tested per EN 204 D3 classification protocols.

    When the Wet Laminate Must Survive 72 Hours of Water Soak at 50 °C

    The hydroxyl and carboxyl functionalities distributed across the particle shell enable a graded crosslinking response. With aluminum chloride as an ionic crosslinker at 0.3 wt%, the tensile storage modulus at 80 °C increases by a factor of 2.4, yet the film retains 250 % elongation at break, avoiding the brittleness characteristic of fully zinc-crosslinked polyacrylate systems. Submersion of crosslinked film specimens (cured 7 days at 23 °C and 50 % RH) in deionized water at 50 °C for 72 hours results in a mass uptake of 12–14 % and a retained tensile strength of 6.3 MPa (initial: 8.1 MPa), tested per ISO 527-3 on dumbbell specimens of 200 µm thickness. By comparison, a standard non-carboxylated VAE with identical ethylene content absorbs 24 % water and retains less than 50 % of its original tensile strength under identical conditions. The emulsion is not recommended for continuous immersion in alkaline aqueous media (pH > 10) as the PVOH colloid undergoes hydrolysis, causing irreversible viscosity loss and particle coalescence. GW-706’s co-stabilization with an anionic surfactant at a low concentration (0.2–0.5 wt% on total emulsion) reduces surface tension to 38–42 mN/m. This enables wetting on contaminated wood substrates where dust extracts inhibit film spreading. In a production-scale floor adhesive line employing a planetary mixer with a 500 L capacity, the addition of 200 phr calcium carbonate filler (D50 = 10 µm) to GW-706 yields a Brookfield viscosity (ISO 2555, spindle 7, 20 rpm) of 85,000–110,000 mPa·s. The filled compound remains pumpable through a progressive cavity pump at 15 L/min without cavitation, while the thixotropic recovery is complete within 120 seconds, preventing slump on vertical notched trowel applications.

    Rheological Fingerprint and Coating Line Processing Windows

    The flow curve of GW-706, captured on a controlled-stress rheometer at 23 °C with a 40 mm cone and angle, exhibits a zero-shear viscosity of 350 Pa·s and a power-law index of 0.42 across the shear rate range of 1–1000 s⁻¹. This shear-thinning profile permits direct transfer from a storage IBC toter via a diaphragm pump and subsequent smoothing on a curtain coater operating at a curtain height of 100 mm without curtain breakup. When the emulsion is pre-heated to 35 °C, the viscosity curve shifts downward by approximately 45 %, yet the dynamic surface tension at 100 ms bubble lifetime (measured by maximum bubble pressure tensiometry) remains above 45 mN/m, indicating that the PVOH colloid dominates surface aging rather than low-molecular-weight surfactants. This property is critical for minimizing foam generation in high-speed roll application lines exceeding 80 m/min web speed.

    Comparative Data Against Standard VAE and Acrylic Dispersions

    The selection of GW-706 over a commercial styrene-acrylic copolymer dispersion for a particular application often hinges on the trade-off between UV stability and block resistance. The following table documents comparative mechanical and physical properties after 14-day ambient conditioning.
    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
    The higher peel adhesion on polyethylene derives from the optimized particle morphology rather than from bulk ethylene content. The shear adhesion failure temperature (SAFT) of GW-706 exceeds that of a chemically similar random copolymer by 24 °C, attributable to the reinforcement of the continuous PVOH phase that forms upon film formation. Compliance with indirect food-contact regulations is documented under FDA 21 CFR 175.105 and 176.170 for the use of GW-706 in laminated paper and paperboard for aqueous and fatty foods. Migration testing per EU Regulation 10/2011 with simulant D2 (vegetable oil) at 40 °C for 10 days returned total migration below 3 mg/dm². The product is free of added alkylphenol ethoxylates (APEOs) and formaldehyde donors. Residual vinyl acetate monomer content is controlled via post-polymerization thermal stripping to less than 300 ppm, verified by headspace gas chromatography with flame ionization detection per ISO 6401:2008. In nonwoven construction, spray application through a 0.8 mm nozzle at 2.5 bar atomizing air pressure produces a uniform fiberized pattern without spitting, a failure mode traced to excessive elastic modulus in the emulsion that GW-706 avoids because of its moderate high-shear viscosity of 120 mPa·s at 10,000 s⁻¹. The open time on a porous substrate at 35 °C and 60 % RH measures 45 seconds, providing sufficient repositionability for core-winding applications.

    Storage Stability, Incompatibility Boundaries, and High-Temperature Limits

    Shelf life at 5–35 °C in sealed containers extends to 12 months. Freeze-thaw stability is rated at 3 cycles from −5 °C to 23 °C without coagulation, after which the viscosity increases by 20–30 %. Formulators must avoid the addition of polyvalent metal salts (Al³⁺, Zn²⁺, Ca²⁺) at concentrations exceeding 0.5 wt% of the total formulation without the presence of a sequestering agent, as instant gelation occurs due to bridging of the carboxylated latex particles. Combination with amine-based pH adjusters such as AMP-95 must be performed under high agitation; the pH of GW-706 as supplied is 4.5–5.0, and rapid neutralization above pH 7.5 causes a transient viscosity spike exceeding 50,000 mPa·s before the system re-equilibrates. The emulsion has been successfully employed in a twin-screw compounding extruder (L/D 40:1) for the preparation of thermoplastic hot-melt adhesives when co-fed with a solid ethylene-vinyl acetate (EVA) copolymer at a 30:70 dry blend ratio, with the screw speed limited to 200 rpm to prevent premature crosslinking at the die.