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Anhui Liwei Chemical Co., Limited.

Redispersible PVAc Homopolymer Powder

    • Product Name: Redispersible PVAc Homopolymer Powder
    • 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 414021
    Product Type Redispersible PVAc Homopolymer Powder
    Chemical Composition Polyvinyl acetate homopolymer
    Physical Form Free-flowing white powder
    Particle Size 80-100 mesh
    Glass Transition Temperature 15-20 °C
    Minimum Film Forming Temperature 5-10 °C
    Ph Of Redispersion 4.0-6.0
    Brookfield Viscosity 10 Solution 500-2000 mPa·s
    Bulk Density 400-600 g/L
    Moisture Content ≤ 1%
    Redispersibility Excellent upon water addition
    Protection Colloid Polyvinyl alcohol (PVOH)
    Shelf Life 12 months from production if stored properly

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

    Packing & Storage
    Packing 25 kg kraft paper bags with inner polyethylene lining, moisture-protective sealed packaging for Redispersible PVAc Homopolymer Powder.
    Container Loading (20′ FCL) Redispersible PVAc powder packed in bags, palletized, loaded into 20-foot container for efficient, safe FCL transport.
    Shipping Redispersible PVAc Homopolymer Powder ships as a free-flowing white powder in moisture-proof laminated bags or drums. Protect from moisture, humidity, and direct sunlight. Store cool and dry. Non-hazardous, but avoid dust inhalation. Ensure secure palletization and dry container transport to preserve quality.
    Storage Store in a cool, dry, well-ventilated area away from direct sunlight and moisture. Keep containers tightly sealed when not in use to prevent caking or polymer degradation. Avoid exposure to extreme heat or humidity. Use within specified shelf life, typically 6–12 months, ensuring original packaging remains undamaged.
    Shelf Life Shelf life is typically 12 months from manufacture when stored unopened in a cool, dry place, protected from moisture.
    Application of Redispersible PVAc Homopolymer Powder

    In a factory-mixed gypsum joint compound based on β-hemihydrate plaster, calcium carbonate, perlite, rheology modifiers, and a set retarder, 1.0–3.0 wt% of redispersible PVAc homopolymer powder relative to the total dry mix is added as a dry binder. The powder is produced by spray-drying a polyvinyl acetate homopolymer latex that contains a polyvinyl alcohol protective colloid; after redispersion in water at a water-to-powder ratio of 0.40–0.50, the polymer particles coalesce during the drying phase and form a continuous film between gypsum crystals and filler particles. This film contributes to wet-edge retention and reduced surface microcracking, but the harder polyvinyl acetate homopolymer film also raises the stiffness of the dried compound and therefore requires careful balancing against the sanding performance specified in ASTM C474-20, with final product classification under ASTM C475/C475M-20 or EN 13963:2014 for the European market.

    On a 200 L Lödige FM-130 ploughshare mixer operating at 90–120 rpm, the PVAc powder is introduced after the fillers and before the cellulose ether to avoid localized binder accumulation on the vessel wall. Batch-to-batch moisture is checked by Karl Fischer titration and held below 1.5 wt%; when ambient storage relative humidity exceeds 60%, the powder is pre-dried at 40 °C before blending to prevent sieve blockage in the packaging circuit. The finished dry mix is rehydrated at the jobsite with 0.40–0.50 L water per 1 kg powder, mixed for 3–5 min at 600–900 rpm, and applied with a stainless steel trowel. Over-addition beyond 4.0 wt% produces a compressible film under knife pressure, and sanding with 220-grit abrasive can generate surface gumming and non-uniform gloss after priming; this failure mode is observed on production lines as a longer sanding cycle and higher rejection of painted boards. Terminal products include factory-mixed all-purpose joint compounds, lightweight joint compounds, topping compounds, and dry skim coat fillers.

    How Does Redispersible PVAc Homopolymer Modify Water Demand in Interior Powder Skim Coats?

    The water demand of an interior powder skim coat is not a fixed function of PVAc homopolymer loading; formulators determine it with a mini-slump cone before scale-up. At addition rates of 1.5–4.0 wt% of the total dry mix, the polymer can increase paste viscosity because of the high molecular weight of the redispersed polyvinyl acetate, and the water-to-powder ratio is typically adjusted between 0.32 and 0.40. The powder acts as a film-forming binder at the interface between the skim coat and a porous concrete or gypsum substrate, and the coalesced film contributes to adhesion values measured under ISO 4624:2016 after 7 days at 23 °C and 50% RH. For EU specifications, the product is assessed under EN 15824:2017 as an internal plaster or render; for China-bound interior wall putty, GB/T 23455-2009 is the routine classification standard. The powder is not suitable for exterior alkaline renders or lime-cement plasters where prolonged pH values above 11 accelerate hydrolysis of the acetate ester and reduce wet bond strength.

    ApplicationStandard designationKey measured property
    Gypsum joint compound and fillerASTM C475/C475M-20Bond strength, shrinkage, crack resistance
    Gypsum joint compound and fillerEN 13963:2014Adhesion, sandability, surface hardness
    Interior skim coat under paintISO 4624:2016Pull-off adhesion after 7 days at 23 °C/50% RH
    Interior wall putty for China marketGB/T 23455-2009Bond strength, water resistance, sandability

    Production-scale blending is carried out in a vertical cone blender with a working capacity of 500–1,000 L; the PVAc powder is added by loss-in-weight feeder at a rate not exceeding 0.5 kg/min per 100 kg dry batch to prevent dust stratification. The jobsite application process requires a high-dispersion mixer at 600–900 rpm, followed by a 5 min maturing period; airless spray equipment is operated at 180–220 bar for large areas, while stainless steel trowels are used for thin repair skim coats. The dry film becomes tacky if ambient temperatures are below 10 °C because the polyvinyl acetate homopolymer has a higher minimum film-forming temperature than VAE copolymers; this is a known boundary condition for unheated job sites. Terminal products include interior high-build skim coats, renovation fillers, paintable wall putty, and decorative base coats for low-alkali substrates.

    In an interior calcium sulfate/gypsum flowable floor fill, 1.0–4.0 wt% of redispersible PVAc homopolymer powder is dry-compounded with α-hemihydrate gypsum or anhydrite binder, fine limestone filler, polycarboxylate superplasticizer, defoamer, and lithium carbonate accelerator. The polymer powder reduces the tendency of the freshly mixed screed to form a dry surface crust while spread flow is measured with a 200 mm ring; water is adjusted within 0.20–0.26 L/kg dry powder to achieve the required flow class under EN 13813:2002. When the binder system is calcium sulfate, product requirements are specified under EN 13454-1:2004, while ASTM C1708/C1708M-20 is used for project specifications written around hydraulic cement self-leveling mortars. The PVAc homopolymer is not recommended for ordinary Portland cement-rich self-leveling underlayments because the pore solution pH above 13 can hydrolyze the acetate ester, and published data for this specific high-alkali configuration is limited.

    The dry-blend process uses a double-shaft compulsory mixer with discharge temperature held below 45 °C to avoid premature agglomeration of the PVAc powder. At the pump line, a continuous gypsum machine feeds the mixed slurry to an eccentric screw pump at 10–25 mm lift thickness; a spike roller is passed over the wet surface within 10–15 min to release entrained air. If the PVAc homopolymer loading exceeds 5 wt%, the surface can remain soft and compressible beyond the normal foot-traffic window of 4–6 h, and the compound can become difficult to spike-roll without tearing; this operational failure is observed on projects where the dosing system is not calibrated for the additional powder bulk volume. Terminal products include self-leveling underlayments for luxury vinyl tile, laminate, carpet, and ceramic tile installation, as well as renovation layers over existing concrete, timber, and old screed substrates.

    When PVAc Homopolymer Powder Is Reconstituted for EN 204 D2 Wood Assembly

    When a dry-mix wood adhesive is prepared for non-structural interior assembly, the redispersible PVAc homopolymer powder is used as the primary binder at 70–90 wt% of the dry formulation. The remaining dry components are calcium carbonate filler, a polyvinyl alcohol rheology modifier, and a defoamer. The powder is dispersed in water at a powder-to-water mass ratio between 1:0.8 and 1:1.1, and the resulting adhesive is conditioned for 10 min before use to allow complete redispersion and air release. The cured adhesive is classified under EN 204:2016 for D1/D2 non-structural interior dry-service applications; tensile shear strength is measured according to EN 205:2016 or ASTM D905 using beech or beech veneer substrates after conditioning at 23 °C and 50% RH. D3 and D4 wet-service categories require additional crosslinkers or alternative copolymers because the unmodified polyvinyl acetate film loses strength under sustained moisture exposure.

    In production, the dry powder adhesive is reconstituted in a high-shear mixer at 1,500 rpm for 10 min, then applied by roller coater at 100–150 g/m² on one or both faces. The open time before assembly is 5–10 min at 20 °C; the stack is cold-pressed at 0.5–1.0 MPa for 20–30 min, followed by 24 h cure under controlled humidity. If the press pressure is below 0.3 MPa, the adhesive line can remain open and produce spring-back in 18 mm particleboard or MDF lamination; this failure is observed as a visible edge gap after trimming. Terminal products include veneer laminating, edge-glued panels, finger joints in interior furniture, decorative MDF/HDF laminating, and non-structural wood parts. The powder should be stored in sealed silos; if exposed to relative humidity above 60%, it should be predried at 40 °C before dry blending to prevent lumping in the screw feeder.

    Standard designationScopePVAc homopolymer boundary condition
    EN 204:2016Classification D1-D4 non-structural thermoplastic wood adhesivesUnmodified PVAc powder meets D1/D2 interior dry-service; D3 requires additional crosslinking
    EN 205:2016Tensile shear test method for wood adhesivesConditioning at 23 °C/50% RH for 7 days; substrate species must be reported
    ASTM D905Adhesive bond shear strength by compression loadingHardwood data cannot be transferred to MDF or particleboard without separate validation

    A paper-to-paper lamination adhesive in dry powder form is produced with 75–90 wt% redispersible PVAc homopolymer powder; the dry mix is reconstituted with water at a powder-to-water mass ratio of 1:0.6–1.0 to reach a Brookfield RVT viscosity of 2,000–4,000 mPa·s at 20 °C, measured with spindle 4 at 20 rpm. The redispersed latex is applied to the moving paper web at 60–120 g/m² by engraved roller or doctor blade. When the dry film is used in food contact, it is evaluated under FDA 21 CFR 175.105 as an indirect food additive; for European Union conversion, migration testing is conducted according to Regulation (EU) No 10/2011, and for China-bound exports, GB 9685-2016 governs the permitted use of adhesive additives. The PVAc homopolymer does not require solvent, and the dry powder formulation can be shipped without the preservative load of a liquid latex.

    On a high-speed web laminator, line speed is maintained between 50 and 150 m/min; nip pressure is set at 0.3–0.7 MPa to avoid adhesive strike-through on lightweight paper grades. The joined web is passed through a hot-air or infrared drying section before reel-up to remove residual moisture. At speeds above 150 m/min, the adhesive can produce tailing at the rear edge of the coated area if viscosity exceeds 4,000 mPa·s; formulators control this by including 0.2–0.5 wt% carboxymethyl cellulose or by raising the water ratio within the stated range. Terminal products include multi-wall paper sacks, laminated paperboard, spiral-wound paper tubes, carton side seams, and envelope seams. The dry adhesive should not be combined with polyvalent metal salts known to destabilize polyvinyl alcohol-protected PVAc dispersions, because this can produce grit and block the coating roller cells.

    Spray-Grade Gypsum Plaster Requires Reduced Air Entrainment Through PVAc Powder Modification

    Machine-applied gypsum plaster receives 0.5–2.0 wt% redispersible PVAc homopolymer powder relative to the dry plaster weight. The powder is introduced after the fine gypsum and before the starch ether in the dry-blending sequence to prevent dusting and to avoid binder agglomeration inside the continuous sieve mixer. The redispersed polymer forms a low-tack film that reduces surface dusting after sanding and improves the cohesion of the wet mix during spray application. The finished plaster is tested under EN 13279-1:2008 and EN 13279-2:2014; project specifications in North America may reference ASTM C842 for interior gypsum plaster application, but the product standard remains the EN 13279 series for EU trade. The addition level is held below 2.0 wt% because higher loadings can lower the compressive strength of the set gypsum body; published data for spray-grade plaster with PVAc homopolymer above 2.0 wt% is limited.

    The application line uses a m-tec M300 or Putzmeister MP 25 continuous mixing pump set to a water-to-powder ratio of 0.20–0.35 L/kg; the mix is sprayed at 8–15 mm lift thickness and floated after 10–20 min to close surface pores. The pump operator adjusts the water ratio within the range to keep slump at the spray nozzle below the threshold that causes sagging on vertical surfaces. At 1.5 wt% PVAc powder loading, the material shows a more even spray pattern and less pulsation-induced sag, but the mixing torque may increase if the powder is added after the water rather than dry-blended with the plaster. Terminal products include machine-applied gypsum base coat, spray-applied finishing plaster, decorative moldings, and pre-cast gypsum elements. The dry mix should be stored at relative humidity below 60%; if lumps are detected in the silo, the material should be screened through a 0.8 mm mesh before the pump hopper to prevent nozzle blockages.

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    Certification & Compliance
    More Introduction

    Redispersible PVAc homopolymer powder is a spray-dried thermoplastic powder obtained from a poly(vinyl alcohol)-stabilized polyvinyl acetate dispersion. During drying, primary polymer particles of 1.0–8.0 µm mean diameter are embedded in a water-soluble poly(vinyl alcohol) matrix and surface-treated with a mineral anti-caking component at addition levels of 8.0–12.0% by dry weight. When the powder is added to water under low to moderate shear, the protective colloid dissolves and re-emits the original polymer particles as a dispersion measured by laser diffraction according to ISO 13320-1:2020. The homopolymer composition has a glass transition temperature of 28–33 °C and is not internally plasticized; minimum film formation temperature is therefore higher than that of ethylene-modified VAE powders. Representative commercial designations in the homopolymer class include R-PVAc-H 120 and R-PVAc-H 180, where the suffix denotes the nominal bulk density band and anti-caking intensity is adjusted to maintain free flow. These grades are selected for low-alkali construction products requiring rigid film strength rather than flexibility.

    What Limits the Redispersibility of PVAc Homopolymer Powder at High Mixing Energy?

    Redispersion quality is a shear-history-dependent property rather than a fixed material constant. In continuous high-shear mixers operating above 1000 s⁻¹, the released PVAc particles can coalesce into coarse agglomerates larger than 200 µm, which reduces film continuity at the substrate interface. Production-scale observation in a 500 L planetary mixer at 80 r/min shows that direct addition into the water vortex without mineral preblending raises residue on a 250 µm sieve to 2.5–4.0%, while preblending the powder with filler for 60 s before water addition lowers the same residue below 1.0%. Water temperature outside the range of 10–30 °C slows dissolution of the poly(vinyl alcohol) protective colloid or accelerates particle aggregation. Borate-based additives disturb the protective colloid through borate-diol complexation and increase the coarse fraction; such additives are excluded from formulations where redispersion quality is a release criterion. For continuous thin-bed mixing units, the powder should be metered with a loss-in-weight feeder into the dry-filler stream rather than directly into the wet paste.

    The redispersed aqueous dispersion at 20% solids and 20 °C typically shows Brookfield viscosity of 500–2500 mPa·s at 20 r/min with spindle 4 according to ISO 2555. The dispersion is shear-thinning; apparent viscosity at 100 s⁻¹ falls to 200–800 mPa·s. These viscosity values depend on the poly(vinyl alcohol) degree of hydrolysis and molecular weight as well as on the anti-caking mineral type.

    Specification Limits for a Spray-Dried Homopolymer Grade

    Typical values in this section reflect publicly available technical data for homopolymer PVAc redispersible powders; exact acceptance limits vary by manufacturer and grade. The specification framework is used to separate usable powder from material that has been exposed to excessive moisture or heat during storage.

    PropertyTypical range or limitTest methodOperational note
    Dry powder appearancewhite to off-white free-flowing powdervisual inspectionno hard lumps after storage at 25 °C and 60% RH
    Bulk density450–650 g/LDIN EN ISO 60grade-dependent; R-PVAc-H 120 is at the lower band
    Residue on 315 µm sieve≤ 2.0%ISO 2591-1air-jet sieving for 2 min
    Non-volatile content≥ 98.0%ISO 3251105 °C to constant mass
    Ash content8.0–12.0%ISO 3451-1method A, 450 °C
    pH of 10% aqueous dispersion4.0–6.5ISO 976after 24 h stabilisation
    Glass transition temperature28–33 °CISO 11357-2second heating, 10 K/min
    Minimum film formation temperature15–20 °CISO 2115unplasticized film
    Mean particle size after redispersion1.0–8.0 µmISO 13320-1laser diffraction, water
    Residual vinyl acetate monomer≤ 1000 mg/kgheadspace gas chromatography, internal methodlow-VOC classification support

    In gypsum-based skim coats and hand-applied joint compounds, addition levels of 1.0–4.0% by dry formulation mass are used to increase adhesion to plasterboard, reduce surface checking, and raise surface hardness after drying. The mechanical contribution is evaluated by bond strength testing under EN 13279-1 or by edge cracking resistance under ASTM C474; published data for this specific configuration is limited, and the dose-response curve is strongly affected by the filler package. Drying conditions below 15 °C or relative humidity above 70% delay PVAc film coalescence and reduce the stiffness contribution. In cement-bonded patching mortars and indoor tile adhesives, the homopolymer powder is typically limited to 1.5–3.0% by dry mass because hydrolysis of acetate side groups in moist alkaline conditions reduces wet strength over time. Formulators use PVAc homopolymer where rigid set and high tensile strength are required, and ethylene-modified VAE or acrylic powders where flexibility, water resistance, or exterior durability are dominant.

    Because the polymer is not film-forming below 15 °C, application of PVAc homopolymer in dry-mix products intended for cold-weather use requires a coalescing aid or external plasticizer. Common coalescing agents include ester alcohols at 1.0–2.0% on polymer solids; the exact dosage is determined by minimum film formation temperature testing under ISO 2115. Without a coalescing aid, film formation on a substrate at 10 °C is incomplete and leads to low adhesion and microcracking.

    When PVAc Homopolymer Replaces VAE Copolymer in Low-Alkali Adhesive Formulations

    Substitution of PVAc homopolymer for VAE copolymer is not a one-to-one weight replacement. A homopolymer grade with Tg 28–33 °C yields higher tensile strength and lower elongation than a VAE powder with Tg −10 to +10 °C. In dried film evaluations according to ASTM D638-14 at 23 °C and 50% RH, homopolymer PVAc films typically show tensile strength of 8–14 MPa and elongation at break of 5–15%, whereas VAE films commonly fall between 2–5 MPa tensile strength and 400–900% elongation. The homopolymer is selected for rigid adhesion, high surface hardness, and resistance to cold flow, but it is not used where movement accommodation or water immersion is required. Water absorption after 24 h immersion is higher than that of VAE and acrylic powders, and the PVAc film can whiten irreversibly in continuous water contact.

    PropertyPVAc homopolymer RDPVAE RDPVAc/VeoVa RDP
    Glass transition range28–33 °C−10 to +10 °C5–20 °C
    Minimum film formation temperature15–20 °C0–5 °C0–8 °C
    Film tensile strength8–14 MPa2–5 MPa5–8 MPa
    Elongation at break5–15%400–900%200–400%
    Water resistancelower; film whitening after 24 h water contacthighermoderate
    Alkali resistancemoderate to low; hydrolysis risk above pH 12higherhigher
    Primary usegypsum fillers, rigid low-alkali adhesivesflexible tile adhesives, waterproofing membranesexterior plasters, ETICS/EIFS base coats

    The water-sensitivity difference is critical in tile adhesives classified under EN 12004. PVAc homopolymer film loses bond strength after water immersion because acetate side groups hydrolyse slowly in alkaline water. For a C2 classification, ethylene-modified VAE or VAc/VeoVa powders are used because they maintain tensile adhesion after water immersion above 0.5 MPa. Published data for PVAc homopolymer alone in this specific test is limited, and it is not recommended as the sole polymer for permanent water-immersion classes.

    PVAc homopolymer also differs from acrylic and styrene-acrylic redispersible powders. Acrylic powders provide lower water absorption and better exterior durability, but lower polar adhesion to cellulosic substrates. PVAc homopolymer provides stronger adhesion to paper-faced gypsum board and wood-based materials, which is exploited in gypsum joint compounds where adhesion to paper facing is a controlling requirement. In exterior applications, PVAc homopolymer is not recommended because repeated wet-dry cycling and ultraviolet exposure degrade the acetate polymer chain.

    Bulk storage of the powder in outdoor silos without dehumidification is a common source of batch-to-batch performance drift. At 25 °C and 60% RH, equilibrium moisture uptake remains below 1.0%, but exposure above 70% RH for 48 h can increase the coarse fraction and reduce redispersion quality. Silos should be fitted with a drying air supply maintaining a dew point below −10 °C. In screw conveying, the powder can compact at bulk densities above 650 g/L; rotary valves should be sized for the lower bulk density to avoid bridging. Storage stability is typically specified as 12 months in unopened original bags at 5–35 °C. Formulation incompatibilities include borate-gelled poly(vinyl alcohol) systems and high concentrations of soluble aluminum salts, which destabilize the redispersed polymer. Calcium sulfate hemihydrate, hydrated lime up to moderate pH, and dolomitic fillers are generally compatible. Strong alkaline accelerators such as sodium silicate at pH above 12 accelerate hydrolysis of acetate side groups and should be avoided.