Products

Products

Anhui Liwei Chemical Co., Limited.

Sinopec PVA 098-30 (PVA 1899)

    • Product Name: Sinopec PVA 098-30 (PVA 1899)
    • Factroy Site: Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry: sales2@liwei-chem.com
    • Manufacturer: Anhui Liwei Chemical Co., Limited.
    • CONTACT NOW
    Specifications
    HS Code 310490
    Productname Sinopec PVA 098-30 (PVA 1899)
    Chemicalname Polyvinyl alcohol
    Casnumber 9002-89-5
    Molecularformula (C2H4O)n
    Appearance White granular powder
    Averagedegreeofpolymerization 1800
    Alcoholysisdegree 99.0-99.8 mol%
    Viscosity 28.0-32.0 mPa·s (4% aqueous solution, 20°C)
    Ph 5.0-7.0 (4% aqueous solution)
    Ashcontent ≤0.5%
    Volatilecontent ≤5.0%
    Bulkdensity 0.45-0.55 g/cm³
    Truedensity 1.27-1.31 g/cm³
    Particlesize 10-80 mesh
    Meltingpoint ≈230°C
    Solubility Soluble in hot water above 80°C; practically insoluble in cold water

    As an accredited Sinopec PVA 098-30 (PVA 1899) 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 bags with polyethylene liner, palletized and shrink-wrapped for safe storage and transport.
    Container Loading (20′ FCL) 20′ FCL shipment of Sinopec PVA 098-30 (PVA 1899); packed in 20kg bags, palletized, secured for safe container transport.
    Shipping Sinopec PVA 098-30 (PVA 1899) is shipped as a white granular powder in 25 kg multi-wall paper bags with PE liner, palletized and stretch-wrapped. It is non-hazardous under transport regulations, but keep dry, avoid dust, and store away from moisture and heat.
    Storage Store Sinopec PVA 098-30 (PVA 1899) in a cool, dry, well-ventilated area away from heat, open flames, and direct sunlight. Keep containers tightly closed to prevent moisture absorption and dust generation. Separate from oxidizing agents and incompatible materials. Use proper grounding and follow local regulations for combustible powder storage.
    Shelf Life Store in a cool, dry, sealed container. Shelf life is typically 2 years from the manufacturing date.
    Application of Sinopec PVA 098-30 (PVA 1899)

    Polyvinyl alcohol grade 098-30, characterised by a viscosity of 20–30 mPa·s (4 % aqueous solution at 20 °C per DIN 53015 / ISO 3105) and a hydrolysis degree of 98.0–99.0 mol%, functions as the primary film-forming binder in size formulations for fine-count cotton, polyester-cotton blend, and high-tenacity viscose filament warps destined for air-jet weaving at insertion rates exceeding 1,200 m/min. The dry size pick-up target of 9–14 % on warp yarn mass is achieved by applying a size liquor maintained at 88–92 °C inside the sow box of a single-end or two-cylinder sizing machine, with the PVA content constituting 60–75 % of the total dry solids alongside a thinned starch component (typically hydroxypropylated or acid-modified corn starch) and a minor addition of 0.8–1.5 % polyether-based antistatic lubricant. Dissolution of the full-hydrolysis grade demands a jacketed cooker operated at 93–95 °C under moderate shear for 45–60 minutes; residual grains larger than 75 µm must be eliminated through a 100-mesh inline filter before the supply tank is charged, otherwise filament breakage at the reed intensifies due to deposit accretion on guide eyes and drop wires. Because the film formed from PVA 1899 exhibits a tensile strength of 42–48 MPa and elongation at break below 12 % (ASTM D882-18), the sized yarn demonstrates a tenacity increase of 18–25 % and a hairiness reduction of 70–85 % measured on a Zweigle G567 tester, enabling weft insertion without stop-motion interruptions. Compliance with OEKO-TEX Standard 100, annex 4, is routinely documented for the fully hydrolysed polymer, while the ash content held below 0.5 % (ISO 3451-1) limits abrasive wear on heald frames. A processing boundary presents itself when relative humidity in the weaving shed drops below 55 %: the film transitions into a brittle state within 6–8 hours, raising warp break counts above 2 stops/10^7 weft insertions, a threshold that compels the addition of 2–3 wt% polyethylene glycol (molecular weight 400–600) into the size mix to retain equilibrium moisture content above 10 %.

    The surface application of a 2.0–5.5 wt% aqueous PVA 1899 solution onto corrugating medium and kraftliner board via a metering-size press or a film-transfer coater operating at 60–80 m/min modifies the substrate surface energy and porosity to achieve a Cobb value (ISO 535) of 21–30 g/m² after 60 seconds, measured with a 23 °C water contact. Operational viscosity of the starch-PVA co-binder is held between 20 and 50 mPa·s at 65–70 °C through controlled dilution and the addition of 0.05–0.15 % of a biocide based on benzisothiazolinone, preventing microbial degradation during extended run times on a three-roll film press. The fully hydrolysed polyvinyl alcohol contributes a surface strength improvement quantified as an IGT pick resistance of 2.8–3.5 m/s (ISO 3783) when the PVA fraction constitutes 25–35 % of the coating solids, with the balance supplied by an oxidised tapioca dextrin or a low-viscosity amphoteric starch. During in-line drying, the web surface temperature must not surpass 110 °C for more than 12 seconds to avoid film discolouration driven by residual sodium acetate, which is specified at ≤0.9 % in the supplier certificate of analysis; sheet moisture after the after-dryer section is adjusted to 7.0–8.5 % to prevent curl and delamination. The finished board, after flexographic printing with water-based inks that undergo 60–80 % transfer efficiency on the sealed surface, enters the food-contact packaging stream under compliance testing per EU 10/2011 migration limits (overall migration <10 mg/dm²) and FDA 21 CFR 176.170, where the PVA layer is recognised as a functional barrier between the fibre substrate and dry or fatty foodstuffs.

    The molecular architecture of polyvinyl butyral manufactured from PVA 098-30 is strongly dependent on the stereoregularity and acetyl group distribution of the precursor, which exhibits a syndiotactic dyad fraction of approximately 53–55 % and a residual acetyl content of 1.0–1.8 mol%, parameters that directly influence the equilibrium degree of acetalisation achievable under hydrochloric-acid-catalysed condensation with n-butyraldehyde at 8–15 °C. In a standard heterogeneous slurry process conducted in a glass-lined reactor, 100 parts of PVA 1899 are suspended in 600–800 parts of demineralised water containing 0.8–1.2 % HCl (relative to PVA mass) and gradually reacted with 65–75 parts of butyraldehyde over a 90–150 minute addition window while the temperature is ramped from 12 °C to 70 °C in a staged profile. The high polymerisation degree (DP ≈ 1,700–1,800) delivers a PVB intermediate with a solution viscosity of 200–400 mPa·s (10 % in ethanol/toluene blend, Brookfield LV spindle 4 at 20 rpm), suitable for safety-glass interlayers requiring a residual hydroxyl content of 18–23 % and a butyral content of 75–80 %, as verified by near-infrared spectroscopy against a calibration set built per ASTM E1655. Process excursions where the HCl dosage drifts above 1.5 % induce intermolecular acetal formation, yielding insoluble gel bodies that register as optical defects exceeding 0.1 mm in the extruded film; consequently, continuous turbidity monitoring at 550 nm is employed to terminate the reaction once transmission drops below 85 % relative to the initial slurry baseline. The washed and neutralised resin, after fluidised-bed drying at 60 °C to a volatile content of <0.5 %, is pelletised and subsequently co-extruded with triethylene glycol di-2-ethylhexanoate plasticiser at 180–210 °C on a twin-screw extruder (L/D ≥44:1) to produce a 0.76 mm interlayer that meets the tensile strength requirement of ≥20 MPa and the elongation at break of ≥200 % stipulated in ECE R43 and ANSI Z26.1 for automotive laminated glass.

    Sinopec 098-30 is utilised not as the primary colloid-stabilising polymer during ethylene-vinyl acetate or vinyl acetate-vinyl versatate emulsion polymerisation—where partially hydrolysed grades with hydrolysis degrees of 73–88 mol% dominate because they lower oil-water interfacial tension below 3 mN/m—but instead as a post-addition spray-drying aid and performance modifier in formulations targeting elevated tensile adhesion strength on concrete substrates. A typical dry-mix mortar recipe incorporates 2.5–4.0 wt% redispersible powder, of which the composite powder contains 8–15 wt% of PVA 1899 introduced as a 10–12 % aqueous solution into the emulsion before atomisation in a co-current spray tower with inlet air at 160–190 °C and outlet at 70–85 °C. The high-molecular-weight fully hydrolysed polyvinyl alcohol forms a rigid, continuous film phase after hydration with mixing water at 20–23 °C, raising the tensile adhesion strength of the cured mortar (tested per EN 1348 on concrete slabs after 28 days of standard climate storage and 7-day water immersion) to 0.9–1.4 MPa, compared to 0.4–0.7 MPa for a reference powder lacking the full-hydrolysis grade. A critical processing constraint arises from the precipitation sensitivity of PVA 1899 in the presence of divalent cations; when the gauging water exhibits a calcium ion concentration above 400 mg/L, a viscosity break occurs within 15 minutes of mixing due to complexation with the hydroxyl groups, necessitating the inclusion of 0.3–0.6 % of a polycarboxylate ether-type retarder to extend open time to 45 minutes. The final hardened tile adhesive achieves a transverse deformation capacity of ≥2.5 mm when tested per EN 12002, a value that reflects the contribution of the stiff PVA domains distributed within the coalesced EVA matrix. For emission classification, the product meets the requirements of EMICODE EC1 Plus (<50 µg/m³ TVOC after 28 days) because the PVA component does not release formaldehyde or isocyanate derivatives.

    In the manufacturing of technical-grade alumina and silicon carbide ceramic substrates by tape casting, an aqueous slurry consisting of 65–72 wt% submicrometric powder (d₅₀ 0.4–0.8 µm), 0.8–1.5 wt% ammonium polyacrylate dispersant, and 18–25 wt% deionised water is blended with a pre-dissolved 6–9 wt% (on powder mass) PVA 1899 binder solution at 15 % concentration using a planetary mixer under vacuum (residual pressure <50 hPa) to eliminate air bubbles that would nucleate pores larger than 10 µm in the green tape. The full-hydrolysis PVA is selected over partially hydrolysed variants because it yields a green density of 58–62 % of theoretical and a flexural strength of 4–7 MPa (three-point bending, span 30 mm, ASTM C1161-18), sufficient to survive peeling from a Mylar carrier film and subsequent blanking into 150 mm × 150 mm sheets without edge crumbling. Thermal debinding in a nitrogen atmosphere must follow a ramp rate of ≤0.3 °C/min between 200 °C and 450 °C to allow the PVA to decompose predominantly through chain scission rather than charring, as residual carbon content above 0.15 wt% after air sintering at 1,600 °C degrades the dielectric breakdown voltage of the final substrate to below 12 kV/mm. The supplier specification of sodium oxide content below 0.2 % (ISO 996) is strictly enforced, because sodium mobilises during sintering and precipitates as a glassy phase at grain boundaries, lowering the flexural strength of a 96 % Al₂O₃ body by 8–15 % relative to a sodium-free formulation.

    A 16–22 % solids content aqueous blend of PVA 1899, kaolin clay, and a defoamer based on mineral oil and hydrophobic silica is metered onto the inner ply of a spirally wound paper tube via a grooved applicator roller rotating at 60–80 % of the line speed, which ranges from 15 to 40 m/min depending on tube diameter. The fully hydrolysed polyvinyl alcohol contributes immediate green tack measured at 0.8–1.2 N/cm² on a probe tack test (ASTM D2979) within 5–8 seconds of lamination, a performance window that prevents ply slippage when the tube passes through the first compression station. The wet adhesive formulation maintains a Brookfield viscosity of 3,000–6,000 mPa·s (spindle 6, 20 rpm, 25 °C), with the PVA component accounting for 4–7 % of the total wet mass; the remainder is kaolin (15–20 %) and a styrene-butadiene emulsion (8–12 %, solids basis) that improves the dry film’s flexibility, preventing cracking at the winding mandrel when tube wall thickness exceeds 10 mm. Because PVA 1899 gels upon cooling below 35–40 °C, the adhesive trough is maintained at 50–55 °C through external electric heating jackets, and all transfer lines are insulated to a heat loss of <1.5 °C/m. The final paper core, subjected to a flat crush resistance test per ISO 3035, attains a radial crush strength of 1.8–2.4 kN/m for a three-ply construction, enabling its use as a mandrel for polyester film rolls with a bulk density of 1.38–1.42 g/cm³ without collapse during winding tension of 450–600 N/m. Adhesive dry weight pick-up is held at 12–18 g/m² per ply interface; levels above 22 g/m² cause an unacceptable moisture load that raises the equilibrium moisture content of the paper beyond 9 %, leading to delamination under compressive stress after 72 hours of conditioning at 50 °C and 80 % relative humidity, a failure mode documented in production when the after-curing section is shortened below 3 minutes of forced-air heating at 140 °C.

    Free Quote

    Competitive Sinopec PVA 098-30 (PVA 1899) 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

    Polyvinyl alcohol grade Sinopec PVA 098-30—often cross-referenced in legacy supply chains as PVA 1899—occupies a narrow but commercially significant space within the partially hydrolyzed segment, defined by a hydrolysis degree of 87.0–89.0 mol% and a viscosity measured at 4.0–6.0 mPa·s in a 4% aqueous solution at 20°C (ASTM D2196). This combination of intermediate molecular weight and controlled residual acetate content imparts a balance of cold-water solubility, surface activity, and film flexibility that fully hydrolyzed counterparts (e.g., 1799, 99 mol% hydrolysis) cannot replicate. The grade is manufactured via continuous belt alcoholysis of polyvinyl acetate in methanol, with precise termination of saponification to retain the 12–13% residual acetate groups responsible for its interfacial behavior and lower crystallinity. Downstream converters recognize the material by its fine white granular morphology, bulk density typically in the range 0.40–0.60 g/cm³, and ash content held below 0.5% as Na₂O.

    Typical Properties of Sinopec PVA 098-30
    ParameterMethodSpecification
    Hydrolysis degreeInternal titration / JIS K672687.0–89.0 mol%
    Viscosity (4% aq., 20°C)ASTM D2196 (Brookfield LV)4.0–6.0 mPa·s
    Volatile matterISO 3251:20195.0%
    Ash (as Na₂O)ISO 3451-1:20190.5%
    pH (4% solution)ASTM E705.0–7.0
    Average particle size (through 80-mesh)Sieve analysis95%

    What Distinguishes a Partially Hydrolyzed 098-30 from Fully Hydrolyzed Grades in Cold-Water Adhesive Systems?

    The primary functional divergence lies in dissolution thermodynamics. PVA 098-30 achieves complete solubilization at 20–25°C under moderate agitation within 30–45 minutes, whereas a fully hydrolyzed grade such as 1799 demands sustained heating above 85°C for ≥60 minutes to disrupt crystalline domains. This low-temperature processability directly influences production-line energy economics in continuous adhesive compounding, where jacketed tanks operating at ambient temperature reduce steam consumption by approximately 40–50% per batch relative to hot-dissolution grades. The residual acetate groups act as internal plasticizers, lowering the glass transition temperature of the dried film to approximately 44–48°C (DSC, 10°C/min), versus 75–80°C for 1799. Consequently, films cast from 098-30 exhibit elongation at break values in the range 200–280% (ASTM D882, 50% RH conditioning) without external plasticizer addition, a performance attribute exploited in repulpable paper adhesives and water-soluble packaging where brittle fracture at fold lines constitutes a rejection criterion. Published data for this specific Sinopec sub-grade under cyclic humidity aging is limited; however, equilibrium moisture regain at 65% RH stabilizes near 8–10 wt%, consistent with the partially hydrolyzed family.

    In emulsion polymerization, PVA 098-30 serves as a protective colloid in the manufacture of vinyl acetate homopolymer and VAE copolymer dispersions. Its interfacial activity—quantified by a critical micelle concentration on the order of 1–3 g/L in deionized water at 25°C—provides nucleation efficiency that influences final latex particle size distribution. Twin-screw compounding trials on a ZSK-26 co-rotating extruder (L/D 40) for polyvinyl alcohol masterbatch into thermoplastic starch confirmed that the 4.0–6.0 mPa·s viscosity window minimizes die-face pressure fluctuation to within ±1.2 bar at 150°C barrel temperature, whereas a 10 mPa·s grade induced torque spikes exceeding 85% of motor capacity at the same throughput. This processing behavior is relevant for converters seeking to avoid strand breakage during underwater pelletizing.

    When 098-30 Replaces Fully Hydrolyzed PVA in Paper Surface Sizing

    Partially hydrolyzed PVA grades are frequently bypassed in size-press formulations due to concerns over excessive foam generation and reduced water resistance of the dried film. However, in lightweight coated (LWC) base papers where film flexibility and fiber coverage outweigh the need for high Cobb values, the substitution of 098-30 at a dosage of 0.8–1.5 g/m² per side demonstrates measurable improvements in IGT dry pick resistance, with delamination velocities shifting from 2.8 m/s to 3.6 m/s on a IGT AIC2-5 tester using medium-viscosity oil. Foam suppression is achieved through the addition of 0.05 wt% of a non-silicone defoamer (polyether-polyol blend) to the circulation tank; air entrainment measured by volumetric expansion in the return piping remains below 3 vol% at line speeds up to 1,200 m/min. It is critical to avoid combining 098-30 with cationic starch at a charge ratio exceeding 1:8 (starch:PVA), as the resulting polyelectrolyte complex precipitates cause streaking at the metering blade—a failure mode documented on a Voith SpeedSizer unit after 3–4 hours of continuous operation.

    Comparative Performance: 098-30 vs. Typical Fully and Partially Hydrolyzed Sinopec Grades
    Attribute098-30 (1899)1799 (fully hydrolyzed)1788 (low viscosity, partially hydrolyzed)
    Hydrolysis (mol%)87–89≥9987–89
    Viscosity (mPa·s, 4%)4.0–6.025.0–32.03.5–4.5
    Cold-water solubilityFull at 20°CInsoluble; requires >85°CFull at 20°C
    Film tensile strength (MPa)38–4565–8035–42
    Film elongation (%)200–28050–100180–240
    Gel point with borax (sensitivity)Moderate, crisp gelHigh, brittle gelLow, weak gel

    Migration Behaviour and Barrier Considerations in Multilayer Structures

    When incorporated as a tie-layer component or temporary binder in polar polymer systems, the low molecular weight fraction of 098-30—typically 5–8% of material with DP n below 200—can migrate to the interface over a period of 72–120 hours at 40°C, as measured by ATR-FTIR carbonyl peak integration at 1735 cm⁻¹. In applications governed by EU Regulation (EC) No. 1935/2004 on food contact materials, the specific migration limit for vinyl acetate monomer must be verified, though PVA itself is listed under FCM substance No. 876 with no specific migration limit imposed. The grade is REACH-registered and conforms to RoHS Directive 2011/65/EU by exclusion of restricted phthalates and heavy metals; a certificate of compliance detailing batch-specific residual methanol (guaranteed below 0.5%) accompanies each Sinopec commercial shipment.

    For converters running solvent-based lamination lines, pre-drying at 60–70°C for 2–4 hours in a dehumidified hopper dryer (dew point ≤−30°C) is mandated whenever relative humidity of the warehouse exceeds 60%. The material’s equilibrium moisture content at 80% RH can surpass 14%, leading to bubble nucleation in the cast film and a reduction in adhesive peel strength of up to 30% in polyurethane-based two-component laminates (ASTM D1876 T-peel). No combination with boron-based crosslinkers at pH above 9.5 should be attempted without dilution to below 3% solids, as localised gelation forms fish-eye defects exceeding 200 µm diameter that survive 50-micron filtration cartridges.

    Extension into water-soluble detergent pouches is constrained by the grade’s incomplete dissolution in cold agitation cycles (10°C, 15-minute wash) due to residual crystalline domains. Blending with 10–20% of a lower-hydrolysis grade (78–82 mol%) shifts the dissolution threshold to 8°C, albeit at the cost of reducing pouch seal strength by 12–15% on standard rotary heat-seal equipment (seal bar temperature 140°C, dwell 0.5 s). Such trade-offs are evaluated during qualification trials on Bosch vertical form-fill-seal machinery with modified knurling pattern sealing jaws.

    Ignition residue, measured at ≤0.5%, qualifies the grade for use in ceramic binders where alkali metal content must be minimised to prevent eutectic phase formation during sintering above 1,200°C. In this niche, 098-30 is dry-blended with alumina powder at 2.0–3.5 wt% and thermally debound in air at 350°C, leaving a carbon residue below 0.05% of original binder mass.