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Anhui Liwei Chemical Co., Limited.

Wanwei PVA 24-88(L) (PVA 088-50)

    • Product Name: Wanwei PVA 24-88(L) (PVA 088-50)
    • 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 646264
    Product Name Wanwei PVA 24-88(L) (PVA 088-50)
    Appearance White granular powder
    Degree Of Hydrolysis 87.0-89.0 mol%
    Viscosity 4 Solution 20 C 20.0-28.0 mPa.s
    Ph 4 Aqueous Solution 5.0-7.0
    Volatile Content ≤5.0%
    Ash Content ≤0.5%
    Average Degree Of Polymerization 2400
    Whiteness ≥90%
    Solubility Soluble in hot water, insoluble in common organic solvents
    Cas Number 9002-89-5
    Chemical Formula (C2H4O)n

    As an accredited Wanwei PVA 24-88(L) (PVA 088-50) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in 25 kg multi-layer paper bags with polyethylene inner lining, securely sealed to prevent moisture contamination.
    Container Loading (20′ FCL) Loading of Wanwei PVA 24-88(L) (PVA 088-50) into one 20′ FCL, full container load, palletized and secured for safe transport.
    Shipping Wanwei PVA 24-88(L) is a non-hazardous, water-soluble polyvinyl alcohol powder. Ship in sealed, moisture-proof polyethylene-lined bags or containers to prevent clumping. Keep dry, cool, and away from ignition sources. Avoid dust generation during transport; standard dry cargo container or palletized truckload is suitable.
    Storage Store Wanwei PVA 24-88(L) in a cool, dry, well-ventilated area away from heat, open flames, and strong oxidizers. Keep containers tightly sealed to prevent moisture absorption and contamination. Avoid creating dust clouds. Store at room temperature, protected from direct sunlight, and use within the manufacturer’s recommended shelf life.
    Shelf Life Shelf life is approximately 24 months from manufacture when stored sealed in a cool, dry, well-ventilated area.
    Application of Wanwei PVA 24-88(L) (PVA 088-50)
    In semi-batch vinyl acetate homopolymerization, the selection of a protective colloid controls both latex rheology and the balance between shear stability and film water sensitivity. Wanwei PVA 24-88(L), with a hydrolysis degree of 88 mol% and a 4% aqueous solution viscosity of 24–30 mPa·s (Brookfield LVF, spindle No. 2, 60 rpm at 20°C), is dissolved prior to reaction in a jacketed glass-lined reactor equipped with a pitched-blade turbine (80–120 rpm). The addition level is strictly maintained at 2.5–4.5 wt% of total monomer charge; excursions above 5.0% cause a rapid viscosity climb beyond 80 000 mPa·s (Brookfield RVF, 20 rpm) and impair film clarity due to un-grafted polyvinyl alcohol domains. The residual acetyl content (12 mol%) depresses the crystalline melting point to approximately 180–190°C, enabling grafting via hydrogen abstraction at the methine carbon and creating a PVA-g-PVAc interlayer that stabilizes the dispersion even at solids levels of 55–58%. Temperature ramping from 65°C to 80°C over a 3.5–4.5 h delayed monomer feed period, followed by vacuum stripping of residual vinyl acetate (< 0.1%), yields a homopolymer emulsion with a volume-average particle size below 1.5 µm (laser diffraction, Malvern Mastersizer). The base adhesive conforms to EN 204 durability class D2 for interior woodworking joints and, after plasticization with dibutyl phthalate (5–12% on emulsion weight), meets DIN 68602 for veneer bonding. Wet shear strength on beechwood after 24 h cold-water immersion at 23°C ( EN 205 ) typically falls between 1.8 MPa and 2.5 MPa. Because the partially hydrolyzed backbone re-swells under high humidity, load-bearing exterior assemblies (class D3) require co-formulation with a thermosetting crosslinker—glyoxal at 0.3–0.8% of emulsion weight or a water-dispersible isocyanate—and the pot life shortens to 4–6 h. Processing at ambient relative humidity exceeding 70% extends open-time skinning beyond 15 min and reduces final bondline thickness, demanding press-cycle adjustments. The finished product is a 40–55% solids white dispersion adhesive shipped in IBC totes or drums, used extensively for furniture frame dowelling, paper tube winding, and bookbinding.

    To what extent can a partial-hydrolyzed PVA replace starch in sizing spun polyester/viscose yarns?

    Warp sizing of polyester/viscose blend ring-spun yarns (Ne 20–40) faces a persistent trade-off: starch possesses film strength but inadequate adhesion to hydrophobic polyester, while fully hydrolyzed polyvinyl alcohol adheres well but creates brittle films that dust off during weaving. Wanwei PVA 24-88(L) is integrated into the cook at 50–70% of total dry solids, the balance being a thinned starch such as hydroxypropyl starch or an acrylic size. The size formulation is prepared in a pressure cooker (105–115°C, 20–30 min) and held at 85–90°C in a supply box feeding a Sucker-Müller SMR-type sizing machine. Size add-on is regulated to 8–12% of yarn weight, monitored by an online microwave moisture sensor and controlled through nip pressure at the second squeeze roll (18–25 kN/m of roller width). The tear-down process on a Benninger ZWA sectional warper follows directly after drying on 8–12 Teflon-coated drying cylinders whose surface temperature is cascaded from 130°C to 90°C. The sized yarn exhibits a breaking tenacity improvement of 12–18% and a hairiness index reduction (Zweigle G566) of 40–60% compared with unsized yarn, measured under ASTM D2256 conditions. Oeko-Tex Standard 100 (class I for baby articles) compliance is verified on the dried yarn, and the desizing effluent is monitored for COD (typically 4500–6000 mg/L before treatment) to comply with local discharge thresholds referenced in ISO 14001-certified mill protocols. A noteworthy limitation emerges on 100% polyester filament yarns, where the 88 mol% hydrolysis degree lowers the glass transition temperature enough to cause blocking on the beam under warehouse temperatures above 35°C; under those conditions, the grade is preferentially applied to blend yarns containing at least 30% cellulosic fiber. The end product is a sized warp beam carrying 600–1 200 ends, processed on air-jet or rapier looms.

    Cold-water-soluble laminating adhesives for microwaveable paperboard packaging

    Paperboard lamination for microwaveable and frozen-food folding cartons demands a repulpable bonding layer that remains intact across a temperature range from -20°C to 100°C. A solution of Wanwei PVA 24-88(L) at 20–30% solids is prepared in a top-entering dissolver (EKATO, 1 500 rpm) by gradually sprinkling the powder into water at 25–30°C and then heating to 80–85°C for 45–60 min under vacuum to eliminate microbubbles. The adhesive is transferred via progressive cavity pump to the roller coater pan of a BHS laminator; coating weight is maintained at 3–5 g/m² (dry) on solid bleached sulphate board of 300–450 g/m². After nip lamination and forced-air drying at 120°C, the bond strength exceeds 200 N/m (TAPPI T494, 180° peel), and the glue line withstands 30 min of direct contact with boiling water without delamination. The formulation meets the indirect food contact requirements of FDA 21 CFR 176.170 and the European framework regulation EC 1935/2004 as well as the German recommendation BfR XXXVI for paper and board. Because the PVA 24-88(L) retains a small fraction of unhydrolyzed acetate groups, the adhesive forms a flexible film that does not crack when the carton is creased; however, at relative humidity above 85% the film absorbs 8–12% moisture and the coefficient of friction shifts upward, requiring talc overprint in high-speed form-fill-seal lines. The final articles are microwaveable soup cups, frozen vegetable cartons, and multi-wall sacks for dry pet food.
    Application SegmentKey Regulatory / Conformity StandardCritical Test ParameterTypical Requirement or Value
    PVAc white glue (wood assembly)EN 204 / EN 205Wet shear strength, beechwood, 24 h immersion1.5 MPa (D2 class)
    Sized polyester/viscose warp yarnOeko-Tex 100 (class I) / ISO 14001 mill effluentHairiness index reduction (Zweigle G566)40–60% vs unsized
    Laminating adhesive, microwaveable paperboardFDA 21 CFR 176.170 / BfR XXXVIBoiling water delamination resistance30 min at 100°C
    Dry-mix thin-bed tile adhesive (C1T)EN 12004 / ASTM C1583Tensile adhesion after water immersion0.5 MPa at 28 d
    Redispersible polymer powder (interior)EN 998-1 / JG/T 157Ash content ( 950°C, 30 min )8–12%
    Remoistening envelope adhesiveFDA 21 CFR 176.170Blocking resistance at 50°C, 70% RHNo fiber tear after 48 h
    Direct incorporation of partially hydrolyzed polyvinyl alcohol powder into dry-mix cementitious tile adhesives targets a narrow window between open-time extension and compressive strength loss. Wanwei PVA 24-88(L) is metered into a twin-ribbon horizontal batch mixer (Lödige FKM series, 150–200 rpm) at 0.25–0.60 wt% on total dry blend weight, together with cellulose ether (0.35–0.50%), calcium formate accelerator (0.5–1.0%), and a redispersible polymer powder (2.5–4.0%). The PVA grade is ground to a particle size below 180 µm ( ASTM E11 No. 80 sieve) to prevent fish-eye formation during wet mixing. At a water-to-powder ratio of 0.22–0.26, the addition of PVA 24-88(L) raises the retentive water capacity from 96% to above 99% (filter paper method per EN 1347), which sustains cement hydration on highly absorptive aerated concrete substrates and stabilizes the open time to 25–30 min in dry ambient conditions (23°C, 50% RH). Tensile adhesion after 28 d standard curing followed by 7 d water immersion ( EN 12004 ) increases from a baseline of 0.45 MPa to 0.7–0.9 MPa, largely due to film reinforcement at the tile-substrate interface. However, dosages exceeding 0.8% entrain excessive air (air content measured by EN 1015-7 rises above 8%) and depress compressive strength below the 10 MPa threshold required for EN 13279 class C1 renders. The additive is incompatible with early-strength blends containing high levels of sodium aluminate, which can gel the PVA in alkaline mixing water (pH > 12.5) before hydration adequately progresses. The finished packaged powder (class C1T per EN 12004) is delivered in 25 kg valve sacks for residential and commercial ceramic tile fixing.Spray-drying conversion of vinyl acetate-ethylene (VAE) copolymer dispersions into free-flowing redispersible polymer powders imposes intense thermal and shear stresses on the protective colloid system. Wanwei PVA 24-88(L) is charged into the premix tank as a 10–15% aqueous solution, blended with the VAE latex at a ratio of 6–10 parts PVA (dry) per 100 parts dispersion solids, and diluted to a feed viscosity of 400–800 mPa·s (Brookfield, 100 rpm). The slurry is atomized through a two-fluid nozzle (air cap pressure 1.8–2.5 bar) into a co-current GEA Niro MOBILE MINOR™-type spray tower operated with an inlet air temperature of 135–155°C and an outlet temperature held at 65–78°C. The powder’s glass transition temperature, modulated by the 88 mol% hydrolysis degree, remains close to 25–30°C, necessitating a post-drying fluidized-bed cooling section ( 15–20°C, 10–15 min residence) to suppress caking during packaging. The resulting agglomerated powder exhibits a bulk density of 450–550 g/L (DIN EN ISO 60), an ash content of 8–12% after 30 min at 950°C (EN 1246), and re-disperses within 30 s into a 50 µm film-forming dispersion when combined with water in a standard mortar mixer. Compliance with EN 998-1 for masonry rendering and JG/T 157 for skim coats is verified through peel and shear tests on concrete substrates. Because the 12 mol% residual acetate groups lower the cohesive energy density of the re-formed film, the powder is specified exclusively for interior or sheltered exterior applications; full outdoor weathering classification (e.g., ETAG 004) demands a higher-hydrolysis-grade co-binder (≥ 95 mol%) to raise wet abrasion resistance. The powdery intermediate is fed into factory-blended self-levelling underlayments and repair mortars, where it improves flexural strength and interfacial bond without requiring on-site emulsion handling.

    When remoistening tack must survive repeated freeze‑thaw cycles, narrow‑distribution PVA becomes critical

    Remoistenable adhesives for envelopes and postage stamps operate on the principle of a dried, non-blocking film that regains aggressive tack upon contact with a thin water film. Wanwei PVA 24-88(L) is cooked in a scraped-surface jacketed kettle (FrymaKoruma MaxxD, 85–90°C, 45 min) to a final solution concentration of 35–42% solids, optionally co-formulated with dextrin (10–20% of total solids) to moderate viscosity and with a polyhydric alcohol humectant such as glycerin (3–5% on wet weight) to resist brittleness at low relative humidity. The fluid is deposited on silicone-coated release paper via a reverse roll coater (dry coat weight 12–18 g/m²) and dried through a tunnel oven at 90–105°C to a residual moisture content below 5%. The adhesive layer meets the requirements of FDA 21 CFR 176.170 for incidental food contact when used on the flap of confectionery packaging. Tack measured by a Probe Tack Tester at 2 ms dwell time under 30% RH reaches 3.5–4.0 N after the application of 0.02 g water per 25 cm². Blocking resistance is evaluated by stacking 500 sheets in a conditioning chamber at 50°C and 70% RH for 48 h ( TAPPI T564 ), and no fiber tear is permissible. A known incompatibility exists with boron-containing release coatings: residual borate ions from recycled paper can interact with the diol sequences of 24-88(L) to form a weak gel skin that retards remoistening; therefore, the converting line must verify that the liner is borate-free or apply a barrier lacquer. The final products are high-speed machine-inserted envelopes, stamp sheets, and beverage-label guillotine-cut strips.
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    Certification & Compliance
    More Introduction

    Commodity-grade partially hydrolyzed polyvinyl alcohol marketed under the designation Wanwei PVA 24-88(L) — equivalently coded as PVA 088-50 in some regional indices — is produced by controlled alcoholysis of a polyvinyl acetate precursor with a mean degree of polymerization centered at approximately 2400. The suffix “88” denotes a nominal degree of hydrolysis in the range 87.0–89.0 mol%, yielding a cold-water-soluble film former that retains a fraction of acetate sidegroups sufficient to depress crystalline ordering while preserving strong intra- and inter-molecular hydrogen bonding. A 4% (w/w) aqueous solution at 20°C exhibits a Brookfield viscosity (spindle No. 2, 20 rpm) typically between 48 and 55 mPa·s, as per ISO 15023-2, designating this grade as a high-viscosity, partially-hydrolyzed polyvinyl alcohol. The “(L)” identifier often denotes a low-ash, low-methanol variant suited to adhesives and aqueous coatings where ionic contaminants must be minimized to avoid interference with surfactant or crosslinker stability. The product is supplied as a white-to-creamy granular powder with a bulk density of 0.45–0.55 g/cm³, a volatile matter content not exceeding 5.0% (ISO 3251, 105°C, 3 h), and a residual sodium content controlled to below 0.7% as Na₂O via ISO 3451-1. Aqueous solutions of 4% by weight display a pH between 5.0 and 7.0 and a light transmittance at 650 nm of at least 90%, as determined by the methodology of JIS K6726.

    Key specification parameters and corresponding test standards
    Parameter Typical Value Method
    Viscosity (4% aq., 20°C) 48–55 mPa·s ISO 15023-2 (Brookfield RVT, spindle No. 2, 20 rpm)
    Degree of hydrolysis 87.0–89.0 mol% ISO 15023-2 / JIS K6726 (back titration)
    Volatile matter ≤5.0% ISO 3251 (105°C, 3 h)
    Ash (as Na₂O) ≤0.7% ISO 3451-1 (800°C)
    pH (4% solution) 5.0–7.0 ISO 15023-2
    Transmittance (4% solution, 650 nm) ≥90% JIS K6726

    How Does 24-88(L) Differ from Lower-Molecular-Weight Partially Hydrolyzed Grades?

    Compared with the medium-viscosity type 17-88 (nominal viscosity 20–28 mPa·s at 4%) or the low-viscosity 05-88 (5.0–6.5 mPa·s), the 2400 DP backbone of 24-88(L) delivers markedly higher film tensile strength—above 40 MPa at 23°C and 50% RH when tested per ASTM D882-18—and superior cohesive energy in remoistenable adhesives. The high molecular weight restricts chain mobility during drying, producing a more oriented film structure that resists creep under sustained load ≥2.0 MPa. In contrast, 17-88 is preferred where lower solution viscosity facilitates high-solids sizing formulas (20–25%) with reduced wet pickup, while 05-88 serves niche release coating roles requiring minimal film strength. Unlike fully hydrolyzed PVA such as 24-99 (>98 mol% hydrolysis), the 24-88(L) retains sufficient acetate content to remain fully soluble in cold water without the need for hot cook-up above 80°C, but the film’s water resistance and gas barrier properties are correspondingly lower: oxygen permeability at 0% RH is approximately 8–12 cm³·µm/m²·d·kPa compared with 3–5 cm³·µm/m²·d·kPa for the fully hydrolyzed analog.

    Comparative properties of selected Wanwei PVA grades
    Property 24-88(L) / 088-50 17-88 (1788) 05-88 (0588) 24-99 (fully hydrolyzed)
    Viscosity (4% aq.) 48–55 mPa·s 20–28 mPa·s 5.0–6.5 mPa·s 54–66 mPa·s
    Hydrolysis (mol%) 87–89 86–89 86–89 98–99
    Cold-water solubility Complete at 20°C Complete at 20°C Complete at 20°C Requires heating (>80°C)
    Film tensile strength (dry, 23°C, 50% RH) 40–45 MPa 22–28 MPa 12–16 MPa 42–48 MPa
    Adhesion to cotton under 60% RH High Medium Low Very high

    Water Solubility Profile and Viscosity Build in Aqueous Systems

    At 20°C the polymer hydrates via swelling of amorphous regions without requiring external heat, reaching 90% dissolution within 30 min under mechanical agitation at 200–300 rpm in a baffled vessel. However, complete molecular disentanglement and plateau viscosity are obtained only after 60–90 min of gentle stirring, since prolonged high-shear dispersion above 1000 s⁻¹ can induce foaming and entrap air that adversely affects film clarity. Aqueous solutions of 24-88(L) at concentrations above 8% display pronounced pseudoplasticity; Brookfield LVT readings taken at 6 rpm can be 2.5 to 3 times higher than at 60 rpm. This shear-thinning character is beneficial in roller coating and size-press applications where high transfer efficiency depends on rapid viscosity drop under shearing conditions of 10⁴–10⁵ s⁻¹. Stock solutions formulated at 10% solids and stored at 25°C are prone to skin formation within 48 h unless a small headspace preservative (e.g., 0.1% sodium benzoate) is added. Viscosity drift during storage is typically ≤3% over 72 h when the container is sealed and kept away from direct UV exposure, which can trigger chain scission and gradual molecular-weight reduction.

    When Formulating with Glyoxal or Borate Crosslinkers

    Addition of glyoxal (0.5–2.0% on PVA weight) to a 4% 24-88(L) solution adjusted to pH 4.0–4.5 with citric acid initiates acetal formation, raising the gel point after 4–6 h at 55°C. Pot life at 25°C without pH adjustment remains 8–12 h, permitting single-component adhesive formulations for spiral-wound paper tubes. Borax (sodium tetraborate decahydrate) at concentrations as low as 0.3% induces immediate thixotropic gelation through diol complexation; the gel strength, measured by a falling ball viscometer, increases exponentially with a borax/PVA molar ratio above 0.05. The partially hydrolyzed grade tolerates a slightly wider crosslinker window than fully hydrolyzed counterparts because residual acetyl groups sterically moderate the diol network, but mixing with amine-based additives must be avoided when glyoxal is present to prevent premature Schiff-base crosslinking that can occur within 5 min. Industrial slushing operations on a 1000-L mixing tank with a turbine impeller at 80 rpm observe that local over-concentration of crosslinker near the dip tube often leads to gel grain formation unless the crosslinker is fed through a static mixer directly into the recirculation loop at a rate ≤0.2 L/min.

    Thermomechanical Processing Demands in Film Casting and Extrusion Coating

    Melt processing of 24-88(L) without an external plasticizer is constrained by a narrow thermal window between the crystalline melting point (180–190°C by DSC, 10°C/min) and the onset of thermal degradation, which generates acetic acid and unsaturated aldehydes detectable by headspace GC at 205–210°C. On a co-rotating twin-screw extruder with 40:1 L/D and a vented barrel (zone profile 170/185/195/200/195°C), incorporation of 10–15 phr glycerol plus 2–3 phr stearic acid salt lubricant reduces the melt pressure at the die to 12–15 MPa while maintaining a melt strength sufficient for cast film take-up at 15–20 m/min. The low-ash variant 24-88(L) is preferred because residual sodium acetate above 0.8% catalyses depolymerization, shortening the safe residence time at 200°C to less than 90 s. When co-extruded with ethylene-vinyl alcohol as a tie-layer on a three-layer blown film line with a spiral mandrel die (300 mm diameter, 1.5 mm gap), the PVA layer thickness is typically maintained at 15–25 µm to prevent interlayer delamination arising from differences in moisture expansion coefficients — the PVA layer can swell by 8–12% in the machine direction upon water contact, versus 2–3% for the polyolefin substrate.

    In high-speed warp slashing operations running at 150–300 m/min, the 24-88(L) grade is applied as an 8–10% aqueous size liquor maintained at 85–90°C in the size box, which pressurizes a squeeze nip at 12–18 kN to achieve a wet pickup of 95–120% on cotton/polyester blend yarn. The latent heat of evaporation during dryer contact (cylinder surface temperature 120–135°C) must be balanced against film skinning: if the surface temperature of the size film exceeds 100°C before the core moisture falls below 15%, a brittle shell forms that later dislodges as dust on the loom, lowering weaving efficiency by 3–5% on air-jet looms at 800 rpm. Desizing of woven grey fabric is subsequently accomplished using oxidative pads with hydrogen peroxide 2.0–3.0% owb at 90°C and pH 11.5, achieving residual size content ≤0.2% within 20 min, as verified by trichromatic iodine staining per AATCC 94-2012. The grade’s high DP minimizes re-deposition of size oligomers during the caustic scouring that follows, a distinct advantage over lower-molecular-weight alternatives whose fragments can redeposit on polyester fiber surfaces and resist rinsing.

    Paper surface sizing trials on a puddle-type size press running a 6% solution at 55°C and 80–120 m/min show that 24-88(L) delivers an IGT pick strength improvement of 35–45% over unsized base paper of 70 g/m² when the dry pick-up is held at 1.8–2.2 g/m² per side, measured by ash analysis. Blending with oxidized starch at a 1:3 ratio reduces total sizing cost by 18–22% with a marginal loss in Cobb60 water absorption from 22 g/m² (pure PVA) to 28 g/m² (ISO 535:2014). The partially hydrolyzed grade does not re-crystallize as rapidly as fully hydrolyzed types, so the sized sheets retain higher fold endurance after conditioning at 10% equilibrium moisture, a requirement for multi-pass converting on carton erecting lines that impose 200–250 crease cycles.