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Anhui Liwei Chemical Co., Limited.

General Purpose PVAc Homopolymer

    • Product Name: General Purpose PVAc Homopolymer
    • 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 446567
    Chemical Name Poly(vinyl acetate)
    Cas Number 9003-20-7
    Molecular Formula (C4H6O2)n
    Appearance Colorless to white beads or granules
    Glass Transition Temperature 35 °C (typical, range 30-45 °C)
    Density 1.18-1.19 g/cm³
    Average Molecular Weight 100,000-500,000 g/mol
    Solubility Soluble in acetone, methanol, ethyl acetate; insoluble in water
    Refractive Index 1.466-1.470
    Tensile Strength 20-50 MPa
    Elongation At Break 10-20%
    Softening Point 40-60 °C

    As an accredited General Purpose PVAc Homopolymer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing General Purpose PVAc Homopolymer is packaged in 200 kg drums or 1,000 kg IBCs, ensuring safe containment and handling.
    Container Loading (20′ FCL) 20' FCL: PVAc homopolymer drums loaded on pallets, securely braced and strapped, ensuring safe transport.
    Shipping General Purpose PVAc Homopolymer ships in sealed drums, totes, or bulk tankers. Protect from freezing and extreme heat. Ensure containers are upright, secured, and labeled. Avoid spills; clean with water. No special hazmat classification typically required, but follow standard chemical handling and transportation guidelines.
    Storage Store General Purpose PVAc Homopolymer in tightly sealed, original containers in a cool, dry, well-ventilated area away from direct sunlight, heat, strong oxidizers, acids, and bases. Recommended storage temperature is 5–35°C; avoid freezing. Stir before use and maintain proper stock rotation, as shelf life typically lasts six to twelve months.
    Shelf Life Store in sealed containers at 5–30°C, protected from freezing. Shelf life is typically 12 months from manufacture date.
    Application of General Purpose PVAc Homopolymer

    On a production line assembling beech or oak interior furniture components, the adhesive's open time is governed by emulsion viscosity, PVOH protective colloid concentration, and ambient water loss from the wet film. Commercial general-purpose PVAc homopolymer emulsions in this class are supplied at 50–55 wt% solids with pH 4.5–5.5, Brookfield LVF viscosity of 3000–5000 mPa·s at 20 rpm and 25°C, and a minimum film-forming temperature of 15–18°C when measured by ASTM D2354. The substrate moisture is controlled between 8% and 12% by dry mass before spreading because lower moisture causes rapid skinning and adhesive starvation, while higher moisture slows water diffusion and reduces compression strength. Application is performed with a roller coater or high-pressure piston pump fed nozzle at 0.3–0.8 MPa for softwood and 0.7–1.2 MPa for hardwood. Press time is 20–45 min at 18–22°C; pressure is released only after the adhesive has built sufficient internal resistance to hold the joint closed. Calcium carbonate filler at 5–15 wt% on wet adhesive is added to reduce penetration into open-pore wood; triacetin plasticizer at 2–6 wt% on polymer solids lowers the minimum film-forming temperature but increases creep compliance and reduces dry shear by 10–20%. Without crosslinking, the homopolymer meets dry and lightly humid exposure requirements but should not be specified for EN 204 classes D3 or D4. Destructive evaluation according to EN 205 on beech lap joints conditioned at 20°C/65% RH for 7 days commonly yields dry shear values of 10–14 MPa; values below 10 MPa indicate insufficient spread, starved bondlines, or substrate contamination. Starved joints caused by clamping pressures above 1.4 MPa on softwood show a wood failure percentage below 35% and fail along the interface rather than within the substrate. The finished article moves into edge banding or sanding only after 24 h of ambient conditioning, because residual water plasticizes the polymer and reduces immediate processing strength.

    Compliance and characterization matrix for interior wood assembly using general-purpose PVAc homopolymer
    ParameterTest methodMeasurement conditionOperational significance
    Minimum film-forming temperatureASTM D2354temperature-gradient barsets lower shop-floor limit for film coalescence
    Dry tensile shear strengthEN 205beech lap joints, 20°C/65% RH, 7 daysconfirms adhesive bond integrity
    Durability classEN 204non-structural wood adhesive classificationlimits use to D1/D2 unless modified
    Brookfield viscosityISO 2555LVF sp. 4, 20 rpm, 25°Ccontrols penetration and coat weight
    pHISO 976glass electrode, 25°Cmaintains emulsion stability

    What Process Window Governs Cold Press Lamination of Decorative Veneer with Unplasticized PVAc?

    Decorative beech, oak, and reconstituted veneer lamination to particleboard or MDF uses unplasticized PVAc homopolymer when the fabricator requires low adhesive creep at temperatures from 35°C to 50°C. The veneer is conditioned to 8–10% moisture; the panel core is conditioned to 6–9% to limit differential dimensional movement. Glue is applied on one substrate at 80–120 g/m² with a structured rubber roller of Shore A 30–40. The open assembly time at 20°C and 65% RH is held between 4 min and 8 min; closed assembly can extend to 15 min if the shop floor is below 60% RH. Cold press pressure is limited to 0.2–0.5 MPa. Pressures above 0.6 MPa on veneer thicknesses of 0.4–0.6 mm produce visible bleed-through, especially on oak or ash. Press time is 30–60 min depending on panel format and core temperature. Demolded panels are stacked with slip sheets and conditioned for 24 h before sanding. If a hot press is used at 80–100°C, the thermoplastic character of the homopolymer requires cooling to below 35°C before pressure release; otherwise interfacial slip occurs because the polymer storage modulus is too low to restrain the veneer. Peel testing according to ASTM D903 with 25 mm wide specimens is used to assess bond line integrity; published data for this specific veneer-core configuration is limited, so incoming producibility trials compare peel force against a control adhesive and panel density profile. The homopolymer is not reprocessable after press and has no significant structural post-cure.

    Spiral paper core winding lines require a wet-bond strength envelope that retains the outer wrap before the adhesive film has lost its carrier water. A general-purpose PVAc homopolymer emulsion blended with cooked native starch and kaolin clay is applied by kiss roller or doctor bar to the top ply. A representative wet formulation combines 100 parts of 50–55 wt% solids PVAc homopolymer emulsion with 15–25 parts of cooked starch solution at 20% dry solids, 5–12 parts of kaolin clay slurry at 65% solids, 0.1–0.3 parts of mineral-oil defoamer, and sufficient water to hold Brookfield RVT viscosity at 1500–2500 mPa·s at 30°C when measured with spindle 3 at 20 rpm. The clay filler raises dry solids and blocks rapid liquid migration into high-porosity recycled coreboard; starch contributes wet tack and accelerates skinning after the nip. Spiral tube winders run at 20–60 m/min, with winding tension between 0.2 MPa and 0.5 MPa on the outer ply for standard paper thicknesses. Dwell time before the next layer is often less than 1 s, so wet tack must exceed the peeling moment created by winding tension. Paper moisture is maintained at 6–9% according to ISO 187 and ISO 287. Adhesive penetration is checked by cross-sectioning the finished core after 24 h conditioning at 23°C/50% RH; strike-through to the inside ply is a reject condition because it causes telescoping and loss of axial compressive strength. The terminal product is spiral cores for textile winding, pressure-sensitive tape, flexible packaging, and labels. Axial crush strength is evaluated by ISO 11093-9; ply adhesion is checked by manual peel after conditioning. A highly porous recycled coreboard at 180–220 g/m² may require a higher kaolin loading and a higher viscosity band to prevent dry interfacial failure.

    When PVAc Homopolymer Replaces Starch in High-Solid Carton Side-Seam Adhesive

    On a high-speed folder-gluer processing clay-coated folding carton board at belt speeds from 150 m/min to 300 m/min, a cold-set PVAc homopolymer formulation eliminates the cooking and holding stages required for starch adhesives. The adhesive is prepared by blending 75–85 parts of general-purpose PVAc homopolymer emulsion with 10–20 parts of water, 2–5 parts of benzoate plasticizer, 0.2–0.5 parts of wetting agent, and 0.1–0.2 parts of defoamer. Brookfield RVT viscosity at 30°C is adjusted to 1200–1800 mPa·s at 20 rpm with spindle 3; pH is held at 4.5–5.0 to avoid alkaline degradation of recycled carton board. The glue is transferred through a closed-system wheel or slot nozzle onto the side seam at a bead diameter of 0.3–0.6 mm. The compression belt applies 0.2–0.5 MPa for 1.5–2.5 s; if the compression time is below 1.5 s, spring-back at the side seam increases and the blank may fail in the folder-gluer stacker. Squeeze-out onto printed surfaces is controlled by adding an alkali-swellable thickener at 0.1–0.3 wt% to raise low-shear viscosity without increasing application viscosity. For cartons used in indirect food contact, the adhesive is selected from formulations compliant with FDA 21 CFR 175.105; direct food contact is outside the permitted use of unmodified homopolymer without additional barrier or regulatory review. Finished cartons are transferred to palletizing after 15–30 min, but full bond development requires 24 h. Destructive ear-cut and side-seam shear tests are performed at 23°C/50% RH after conditioning. Because the homopolymer remains thermoplastic, side-seam creep at elevated warehouse temperatures above 40°C can reduce stack stability if the carton is under high lateral load.

    Bookbinding hinge strength and cold-flow limits in adhesive-bound paperbacks

    Adhesive-bound paperback lines use PVAc homopolymer at the primer or body adhesive position when the finished book must retain a stiff spine but not develop brittle hinges during repeated page opening. The homopolymer is plasticized with 10–20 parts of benzoate or triacetin per 100 parts polymer solids to reduce the glass-transition temperature from 28–33°C to 8–15°C, improving low-temperature hinge flexibility. Spine preparation includes scoring and rotary blade roughening to increase surface area; the cold adhesive is applied through a nozzle at 0.3–0.5 mm wet thickness, followed by cover application and pressing at 0.2–0.4 MPa for 3–6 s. The bound block is then stacked under moderate weight for 24 h at 20–25°C before trimming. Page pull and hinge flex endurance are assessed using a tensile testing apparatus at 100 mm/min crosshead speed with a 50 mm clamp width; published standardized method for this specific binder configuration is limited, so incoming inspections compare page pull force and failure mode against an approved control adhesive. At relative humidity above 70%, water sorption plasticizes the homopolymer and shifts the glass transition below typical room temperature, increasing cold flow under the weight of the cover. Repeated opening through 180° at 23°C/50% RH causes hinge fatigue if the plasticizer level is excessive or if the adhesive film was applied below the minimum film-forming temperature. PVAc homopolymer is not used as the sole adhesive in high-speed perfect binding of spine lengths above 120 mm; it is generally combined with EVA or PUR hotmelt for rate and durability. The main operational boundary is moisture: paper with moisture above 10% acts as a heat sink and slows water evacuation from the adhesive film, leaving a soft bondline that can debond during trimming.

    In wallcovering adhesive compounding, a general-purpose PVAc homopolymer emulsion serves as the binder in ready-mixed paste for heavyweight vinyl and nonwoven wallcoverings, where it provides wet tack and dry peel strength without requiring on-site mixing. A wet paste formulation combines 20–40 parts of 50–55 wt% solids PVAc homopolymer emulsion, 0.5–1.5 parts of cellulose ether thickener, 10–20 parts of modified starch, 5–15 parts of calcium carbonate filler, 0.1–0.3 parts of biocide, and water to 100 parts. Helipath T-bar viscosity at 25°C is held between 30,000 mPa·s and 60,000 mPa·s to prevent sag on vertical gypsum wallboard. Application is by notched trowel or paste machine at 150–250 g/m². Open time is 10–20 min at 20–25°C and 50–65% RH. The homopolymer contributes dry peel strength and water resistance greater than starch-only paste, but it remains removable by soaking with warm water containing a small amount of surfactant. Peel strength from gypsum board is measured according to ASTM D903 after 7 days conditioning at 23°C/50% RH. The operational boundary is high moisture: above 95% RH sustained humidity, the unmodified homopolymer softens and may allow wallcovering slip or edge lift; crosslinking or a different binder is required for wet-room installations. The terminal use is interior residential and contract wallcoverings with nonwoven backings, where the adhesive must bridge low-porosity surfaces without blocking the vinyl face.

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    Certification & Compliance
    More Introduction

    Polyvinyl acetate homopolymer in aqueous dispersion is supplied for general-purpose bonding as a white, medium-viscosity liquid with a nominal solids content of 52.0 ± 1.0% by mass and a Brookfield RVT viscosity at 23°C of 3,500 ± 500 mPa·s using spindle 4 at 20 rpm. The product is colloid-stabilized with polyvinyl alcohol and carries a pH of 4.5 ± 0.5 when measured in accordance with ISO 976. As-supplied density is 1.09 ± 0.01 g/cm³ by ISO 2811, and residual vinyl acetate monomer is specified below 0.1% by mass using ISO 13741-1. These values establish the product class designated GP-52, a general-purpose grade intended for cellulosic substrates, packaging, tube winding, and light wood assembly where water resistance class D2 under EN 204 is sufficient.

    In storage, the dispersion is supplied in 200 L polyethylene drums and 1,000 L IBC totes. The aqueous dispersion is not regulated as a flammable liquid, but it remains sensitive to freeze-thaw damage. Storage below 5°C can produce irreversible grit; storage above 35°C accelerates surface skinning in partially filled containers. The preservative system is formulated for pH 4.0–5.0; raising pH above 7.0 with caustic lowers biocide efficacy and destabilizes the polyvinyl alcohol colloidal layer. These are operational boundaries observed in warehouse and drum-handling cycles, not aseptic product claims.

    Specification profile for General Purpose PVAc Homopolymer GP-52
    ParameterSpecification rangeTest method
    Non-volatile matter52.0 ± 1.0%ISO 3251
    Brookfield RVT viscosity, 23°C, spindle 4, 20 rpm3,500 ± 500 mPa·sISO 2555
    pH4.5 ± 0.5ISO 976
    Density1.09 ± 0.01 g/cm³ISO 2811
    Residual vinyl acetate monomer≤0.1%ISO 13741-1
    Particle size, D500.5–2.0 µmISO 13320-1
    Minimum film-forming temperature18 ± 2°CISO 2115

    These specifications are batch-release values, not storage-adjusted results. Viscosity drift during a 14-day warehouse cycle at 30–35°C is typically below ±5% when containers remain sealed; if drums are left open, surface skinning can raise screened residue above 250 µm and create downstream nozzle blockage in roll-coating and jet applicator equipment.

    What Distinguishes a General-Purpose PVAc Homopolymer from VAE and Acrylic Dispersions?

    The dominant structural contrast is the absence of ethylene comonomer. This raises the measured MFFT to 18 ± 2°C, compared with vinyl acetate-ethylene dispersions that frequently report 0 ± 2°C in supplier bulletins. Unplasticized PVAc homopolymer cast films also show higher tensile strength and lower elongation than VAE and acrylic films; observed values under ISO 527-3 typically fall in the 25–35 MPa range with elongation at break below 15%, whereas VAE films are typically below 15 MPa with elongation above 300%. This property cluster makes the homopolymer suitable for rigid cellulosic assembly but excludes applications requiring low-temperature flexibility or elastomeric recovery.

    Typical property comparison derived from supplier technical bulletins for general-purpose aqueous dispersions; values are not specification limits
    PropertyGP-52 homopolymerVAE general-purposeAcrylic general-purpose
    Non-volatile matter, ISO 325152.0 ± 1.0%55.0 ± 1.0%50.0 ± 1.0%
    pH, ISO 9764.5 ± 0.54.5 ± 0.57.0 ± 0.5
    Brookfield RVT viscosity, 23°C, spindle 4, 20 rpm3,500 ± 500 mPa·s1,500 ± 1,000 mPa·s2,000 ± 1,000 mPa·s
    MFFT, ISO 211518 ± 2°C0 ± 2°C5 ± 3°C
    Tensile strength, ISO 527-325–35 MPa5–15 MPa10–20 MPa
    Elongation at break, ISO 527-3<15%>300%>200%

    Film Formation Limits and Plasticizer Migration in Low-Temperature Application

    Below 15°C, the neat GP-52 dispersion forms a discontinuous film because polymer particles cannot complete interdiffusion above their MFFT of 18 ± 2°C. Addition of 3–5% by mass of a phthalate-free ester or benzoate plasticizer lowers the effective film-forming temperature to approximately 5–8°C, but the plasticizer migrates over time under sustained load. In adhesive joints tested under EN 205 after 7 days at 20°C/65% RH, plasticized formulations can show tensile shear strength reduction of 20–30% compared with unplasticized controls. Published data for specific phthalate-free plasticizer systems are limited, but production experience on 1,000 kg mixing batches indicates that pre-emulsification of the plasticizer at 500 rpm in an anchor-stirred vessel prevents local concentration spikes exceeding 10% at the addition point.

    In cold-press wood assembly on beech, the homopolymer is applied at a single-side spread of 120–180 g/m². Open time at 23°C and 50% RH is 8–12 minutes for a 120 g/m² film; closed assembly time up to 20 minutes is tolerable before measurable loss in EN 205 shear strength occurs. Substrate moisture content above 12% slows water absorption and can extend pressing time from 6 minutes to more than 12 minutes at 90°C platen temperature. At platen temperatures above 110°C, surface filming can occur before water migration completes, producing low-strength boundary layers. Most production lines therefore hold 90–100°C for 2–4 mm veneers to balance water removal and thermal cure rate.

    When Aluminium Chloride Accelerator Is Added to a PVAc Homopolymer Bondline

    Aluminium chloride solution at 20% concentration is added at 2.0–5.0% by mass to accelerate setting and improve water resistance. The resulting pH falls to 3.0–3.5, which weakens the steric barrier of the polyvinyl alcohol stabilizer. Pot life can shorten to less than 2 hours; grainy precipitate forms if the mix is left unmixed in a non-agitated container. Mixing should occur in 316L stainless steel or polypropylene vessels, not carbon steel, because iron ions released at low pH can discolour the bondline within 24 hours. An anchor stirrer at 60–80 rpm in a 500 L tank maintains dispersion without imparting high shear; rotor-stator dispersion equipment is contraindicated because it accelerates coagulation.

    Zinc oxide and calcium carbonate fillers are incompatible at addition levels above 1% because their surface alkalinity raises local pH above 8.5 and triggers viscosity build. pH buffering with sodium acetate at 0.2–0.5% before filler addition can extend working life but does not eliminate the incompatibility.

    Rheological Shear Limits Are Not Optional in High-Speed Roll Coating

    On high-speed paperboard lines running at 150–250 m/min, the dispersion is exposed to nip shear rates above 10,000 s−1. The product is pseudoplastic: rotational viscosity at 20 rpm is 3,500 ± 500 mPa·s, but apparent viscosity at 1,000 s−1 drops to 200–400 mPa·s in capillary viscometry reported in supplier technical bulletins. At shear rates above 10,000 s−1, mechanical destabilization can deposit dried skin on roll edges within 40–60 minutes, causing streaking. This failure mode has been observed on pilot lines with 250 mm width steel-to-rubber roll geometry; published data for specific production configurations are limited. Control is maintained by limiting the nip gap to 50–100 µm and by using return-flow pans with recirculation rates not exceeding 2 turnovers/h.

    For tube winding and paper sack manufacture, the homopolymer is diluted with 5–10% water to a flow viscosity of 25–35 seconds in a DIN 4 mm cup at 20°C. The dilution response is not linear: a 10% water addition can reduce Brookfield viscosity by 30–40% at 20 rpm but only 10–20% at 100 rpm. Tap water with hardness above 300 ppm CaCO₃ can interact with anionic surfactants to form insoluble calcium salts; if this occurs, deionized water with conductivity below 50 µS/cm is specified. Cleanup of liquid adhesive uses water at 40–50°C before drying; once the film has coalesced, redispersion is negligible and mechanical or warm 5% acetic acid cleaning is required.

    In radio-frequency edge-gluing of solid wood strips at 27.12 MHz, the homopolymer requires dielectric heating time adjustments because its ionic mobility differs from thermoset adhesives. Process documentation commonly records an additional 15–20% heating time relative to urea-formaldehyde at the same electrode gap of 20–30 mm to reach 70–80°C bondline temperature; published data for this specific configuration are limited. Amine-based urea hardener systems are incompatible with the colloid stabilization and should not be combined with this product.