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Anhui Liwei Chemical Co., Limited.

Sinopec PVA 098-45 (PVA 2299)

    • Product Name: Sinopec PVA 098-45 (PVA 2299)
    • 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 882910
    Product Name Sinopec PVA 098-45 (PVA 2299)
    Chemical Name Polyvinyl alcohol
    Cas Number 9002-89-5
    Appearance White to slightly yellow granular powder
    Degree Of Alcoholysis 99.0-100.0 mol%
    Viscosity 4 Percent Solution 20c 45-55 mPa·s
    Ph 4 Percent Solution 5.0-7.0
    Solubility Soluble in hot water; insoluble in common organic solvents
    Loss On Drying ≤5.0%
    Ash Content ≤0.5%
    Average Molecular Weight ~97000 g/mol
    Bulk Density 0.55-0.75 g/cm³
    Melting Point ~230°C (with decomposition)
    Glass Transition Temperature ~85°C

    As an accredited Sinopec PVA 098-45 (PVA 2299) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sinopec PVA 098-45 (PVA 2299) is supplied in 25 kg net multi-wall paper bags with inner polyethylene liner, palletized and stretch-wrapped.
    Container Loading (20′ FCL) 20′ FCL loading: 20-foot container, palletized PVA bags secured tightly, with dunnage, dry lining, moisture protection, and safe weight distribution.
    Shipping Sinopec PVA 098-45 (PVA 2299) is a white granular polyvinyl alcohol powder, typically shipped in 25 kg multi-layer paper or woven bags. It is non-hazardous and safe to transport by truck, container, or sea freight. Keep cargo dry, avoid excessive moisture, stacking damage, and direct sunlight during transit.
    Storage Store Sinopec PVA 098-45 (PVA 2299) in a cool, dry, well-ventilated area, away from direct sunlight, heat, and ignition sources. Keep containers tightly sealed to prevent moisture absorption and contamination. Avoid generating dust and static discharge. Ensure segregation from oxidizing agents and foodstuffs. Use proper labeling and maintain good housekeeping to preserve product quality and safety.
    Shelf Life Shelf life is approximately 2 years when stored in a cool, dry place in sealed, original packaging.
    Application of Sinopec PVA 098-45 (PVA 2299)

    What Determines the Weaving Efficiency of High-Density Cotton Warp Yarns?

    In high-speed air-jet weaving of fine-count cotton yarns, the warp encounters cyclic tensile loading, yarn-to-yarn and yarn-to-metal friction at heald frames and reed dents, and instantaneous shock loads during shedding. A size film that fails cohesively under these conditions generates lint and dust accumulation on loom elements, triggering weft insertion faults and unplanned machine stops. Sinopec PVA 098-45—a fully hydrolysed polyvinyl alcohol with a 4 % aqueous solution viscosity typically in the range 42–48 mPa·s at 20 °C and a degree of hydrolysis exceeding 99.0 mol%—is deployed in warp sizing because its high average degree of polymerisation translates into a film with a tensile strength above 45 N/mm² and an elongation at break of 120–160 % under ASTM D882-18 test conditions, enabling the size to bridge fibre surface asperites without premature rupture. In a modern multi-cylinder sizing line operating at sizing speeds above 80 m/min, the PVA 098-45 is first dispersed in cold water under high-shear mixing to prevent fisheye formation and then dissolved by indirect steam injection to reach 90–95 °C; the resulting stock solution at 8–12 % (w/w) solids is let down into a final size bath that typically blends the PVA with a degraded or oxidised corn starch, a paraffin-based lubricant at 0.3–0.8 % of total bath weight, and, depending on water hardness, a small quantity (0.05–0.1 %) of a non-silicone defoamer. The size pick-up is controlled by adjusting the squeezing pressure in the immersion roller system so that the dry PVA add-on falls between 8 and 14 % (w/w) relative to the unsized yarn mass. After application, the yarn passes through a wet-split zone and a series of steam-heated drying cylinders with a progressive temperature ramp from 110 °C to 140 °C; a final moisture content of 5–7 % in the sized warp beam prevents brittleness. Compliance with the ZDHC Manufacturing Restricted Substances List Level 2 and conformance to OEKO-TEX ECO PASSPORT certification are verified through extractable heavy-metal and solvent-residue testing on the finished beam. The end articles woven from such warps include combed cotton poplin for dress shirts, mercerised bed-linen fabrics, and polyester-cotton blend twills for institutional uniforms.

    Surface Sizing of Corrugated Medium and Linerboard

    When a corrugating medium machine accelerates beyond 800 m/min, the dynamic surface strength of the sheet as it leaves the size press determines whether starch particles and fibre debris are extracted by downstream vacuum boxes and contaminate the white-water circuit. Surface sizing with a blend of PVA 098-45 and oxidised corn starch improves both the internal bond strength measured under TAPPI T 569 and the water-absorptiveness of the sheet measured as Cobb60 under ISO 535:2023, providing the box plant with a base paper that can withstand the shear and compression forces of conversion without edge cracking. In a film-transfer size press—the predominant configuration for speeds above 1000 m/min—the metering rod or blade transfers a wet film of the PVA-starch size to the sheet surface; the size formulation is prepared by cooking PVA 098-45 at 6–8 % (w/w) solids together with the starch in a continuous jet cooker at 130–135 °C for 10–15 seconds, after which the PVA proportion is adjusted so that the dry PVA-to-starch ratio lies in the range 20:80 to 40:60. The total size-bath solids are maintained between 6 and 10 %, and the wet-pickup on each side is regulated to deposit 0.8–2.0 g/m² dry sizing agent. Post-application, infrared dryers and subsequent drying cylinders bring the sheet moisture to 6–8 % before calendering. For paper and board intended for indirect food contact, the finished product is validated to meet the extractives limits of FDA 21 CFR §176.170 and the European BfR Recommendation XXXVI, with migration testing conducted under the conditions of EU Regulation (EC) 1935/2004. The typical downstream substrates are high-performance test liner, semi-chemical fluting medium, and folding boxboard subsequently converted into corrugated shipping containers, retail-ready packaging, and aseptic brick outer wraps.

    Table 1 – Recommended Starting-Point Formulations for Surface Sizing with PVA 098-45 / Oxidised Corn Starch Blends
    SubstratePVA:Starch Dry Ratio (w/w)Size Bath Solids (%)Target Cobb60 (g/m²)
    High-performance test liner25:75 to 30:708–10< 35
    Semi-chemical fluting medium20:80 to 25:756–8< 50
    Folding boxboard (top ply)35:65 to 40:609–11< 30

    For cementitious tile adhesives classified as C2 according to EN 12004:2017, the incorporation of a powdered polyvinyl alcohol with a hydrolysis degree above 98.5 mol% and a 4 % aqueous solution viscosity exceeding 40 mPa·s provides a mechanism for enhancing wet-out on absorbent substrates and co-modifying the hydration profile alongside cellulose ethers. In factory-produced dry-mix mortars, PVA 098-45 is typically dosed between 0.3 and 1.0 % (w/w) of the total dry blend—comprising ordinary Portland cement CEM I 52.5R, graded silica sand, and a cellulose ether such as methyl hydroxyethyl cellulose—and the mixture is homogenised in a horizontal ploughshare mixer for precisely 180–240 seconds to prevent stratification of the low-density PVA granules. During on-site application, the addition of the specified amount of clean water (20–25 % of dry mortar mass) and mixing with a slow-speed paddle at 400–600 rpm for 2–3 minutes releases the PVA into the aqueous phase, where it partially dissolves and increases the viscosity of the interstitial water, thereby reducing migration of the cement paste into the substrate and prolonging the open time beyond 30 minutes as measured by the wetting method of EN 1346. The contribution of PVA to early-age tensile adhesion strength is assessed after 28 days of standard conditioning by the pull-off test specified in EN 1348; specimens prepared with a 0.6 % addition of PVA 098-45 on a calcium-silicate substrate commonly achieve values above 1.0 N/mm², with the cohesive failure mode indicating good penetration into the tile biscuit. The compliance schedule for such adhesive systems extends to transverse deformation under EN 12002, slip resistance evaluated per EN 1308, and, where applicable, the additional requirements for improved adhesion under freeze-thaw cycling (C2E classification). The final packaged product is a single-component powder supplied by the dry-mix manufacturer and used in kitchens, bathrooms, and external façades for the bonding of porcelain stoneware, fully vitrified tiles, and large-format ceramic slabs onto screeds and plasterboard.

    Table 2 – Harmonized Standard Test Methods Referenced for PVA-Modified C2 Cementitious Adhesives
    PropertyStandard DesignationTest Method Principle
    Tensile adhesion strength (after standard curing)EN 1348:2007Pull-off test on concrete slab with ceramic tile adhered
    Open timeEN 1346:2007Wetting ability after extended mat times
    Transverse deformationEN 12002:2008Three-point bending of notched mortar prism
    Slip resistanceEN 1308:2007Vertical slip under own weight

    When PVB Interlayer Optical Clarity Demands Alkali-Washed PVA

    Starting with PVA 098-45 having a 4 % aqueous solution viscosity above 45 mPa·s, an ash content below 0.7 %, and a methanol-soluble fraction below 0.3 %, the synthesis of optical-grade polyvinyl butyral (PVB) resin proceeds via condensation with butyraldehyde in an aqueous acid-catalysed medium conducted at 15–25 °C. The degree of acetalisation is controlled between 70 and 80 mol%, leaving a controlled density of residual hydroxyl groups that later co-react with plasticiser in the extruded interlayer sheet; the residual acetate groups inherited from the parent PVA—maintained below 0.5 mol% in PVA 098-45—prevent haze formation in the final PVB by minimising random blockiness along the polymer backbone. The crude PVB slurry is neutralised with dilute sodium hydroxide, washed repeatedly until the residual chloride content drops below 50 ppm, and dried under vacuum at 60 °C. Extrusion of the washed PVB flake with 20–35 phr of a long-chain ester plasticiser through a co-rotating twin-screw extruder equipped with a slot die yields a continuous sheet of 0.38–1.52 mm thickness that is immediately laminated between two plies of float glass in a clean-room environment to form laminated safety glass. The finished glazing is certified to meet the optical and mechanical requirements of ECE R43 for automotive windscreen applications and ISO 12543-2:2021 for architectural laminated glass, with the yellowness index measured per ASTM D1003-21 kept below 1.5. The terminal products are automotive windscreens, side and rear laminated glazing for heavy trucks, and laminated glass panels used in balustrades, curtain walls, and hurricane-resistant windows.

    The Role of PVA 2299 in D3/D4 Wood Adhesive Formulations

    Targeting D3 and D4 durability classes under EN 204:2016, formulators of one-component crosslinking poly(vinyl acetate) adhesives incorporate PVA 098-45 as a rheology modifier and additional film-former to improve the cohesive strength of the bond line under intermittent water contact. The PVA is introduced as a 25–30 % (w/w) aqueous solution—prepared by dissolving the granular resin in water at 90–95 °C with slow agitation and then cooling to 23–25 °C—and is blended with the PVAc emulsion at a ratio that delivers 2–8 parts dry PVA per 100 parts of total formulation solids. When an aluminium chloride or glyoxal-based crosslinker is subsequently added at 0.5–2.0 phr, the hydroxyl groups of the PVA co-react with the crosslinker and with the hydrolysed acetate groups of the emulsion, raising the heat- and water-resistance of the cured film. The adhesive is applied with a roller coater or curtain coater onto hardwoods such as beech and oak, assembled within an open time of 5–10 minutes, and pressed in a cold press at 0.8–1.2 N/mm² for 30–60 minutes; for accelerated production, a radio-frequency press with a cycle time of 2–5 minutes may be employed. The bond strength is evaluated after water immersion at 23 °C for 4 days, per the D4 conditioning sequence of EN 204:2016, with a minimum shear strength of 4 N/mm² required on beech substrates. Wood-adhesive compositions of this type, when applied within the constraints of EN 205:2016 for non-structural applications, serve the production of laminated stair treads, edge-glued panels for kitchen worktops, and paperboard spiral tube winding used in packaging cores.

    Managing Viscosity Build-Up in Hot-Water-Soluble Laundry Bags

    In institutional laundry operations where contaminated linens are bagged and dissolved directly in hot-wash cycles above 85 °C, film-grade PVA with a degree of hydrolysis near 99 mol% and a 4 % solution viscosity exceeding 40 mPa·s delivers the necessary balance between delayed dissolution during storage at ambient humidity and complete disintegration during the hot wash. Extrusion of PVA 098-45 for blown film requires pre-drying in a desiccant dryer to a residual moisture content below 0.5 % and dry-blending with 10–20 parts per hundred resin (phr) of a polyol plasticiser such as glycerol or trimethylolpropane, together with 0.5–1.0 phr of a slip/antiblock masterbatch. The dry blend is fed into a single-screw extruder with a barrier screw design and a water-ring or chilled-air blown-film die, operating with a barrel temperature profile of 190–210 °C and a die temperature of 210–220 °C. The bubble is collapsed and wound into tubing or slit to form film rolls, with a thickness tolerance of ±5 µm at a nominal gauge of 35–50 µm. Dissolution testing under conditions simulating a 90 °C alkaline wash (pH 12) demonstrates complete disintegration within 180 seconds, and aerobic biodegradability is confirmed in accordance with ISO 14855-1:2012 using an inoculum sourced from a municipal wastewater treatment plant. The principal commercial article is the hot-water-soluble laundry bag employed in healthcare and infectious-disease containment settings, with secondary use as inner packaging for pre-weighed powdered chemicals that can be charged into processing tanks without the operator breaking the seal.

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    Certification & Compliance
    More Introduction

    Sinopec PVA 098-45, alternately catalogued as PVA 2299 in certain export documentation, is a fully hydrolyzed polyvinyl alcohol resin manufactured via alkaline alcoholysis of polyvinyl acetate. The grade exhibits a nominal degree of polymerization of approximately 900 and a hydrolysis degree spanning 98.0–99.0 mol%. When dissolved at 4% concentration in demineralized water at 20°C, the solution viscosity measured under ISO 2555 (Brookfield LV) stabilizes at 45.0 ± 4.0 mPa·s. Supplied as a white to slightly yellowish granular powder with a bulk density of 0.45–0.65 g/cm³, the product functions as a primary suspending agent in suspension PVC synthesis, a film former in textile warp sizing, a co-binder in paper coatings, and a base polymer in water-resistant adhesive systems. The performance envelope of 098-45 occupies a deliberate intermediate space between low‑viscosity partially hydrolyzed grades such as 088‑05 and high‑polymerization fully hydrolyzed grades such as 1799 and 2099, offering a controlled viscosity–crystallinity balance that low‑DP fully hydrolyzed alternatives cannot replicate.

    Essential Product Characteristics as per GB/T 12010 Series

    Property Test Method Unit Typical Value
    Appearance Visual White to slightly yellowish granules
    Volatile matter GB/T 12010.3‑2010 (oven drying) wt% ≤5.0
    Ash (as Na₂O) GB/T 12010.3‑2010 (muffle furnace 850°C) wt% ≤0.5
    pH (4% solution) GB/T 12010.8‑2010 5.0–7.0
    Viscosity (4% aq., 20°C) ISO 2555 (Brookfield LV) mPa·s 45.0 ± 4.0
    Degree of hydrolysis GB/T 12010.4‑2010 (titrimetry) mol% 98.0–99.0
    Degree of polymerization Calculated from [η] per GB/T 12010.2‑2010 900 ± 50
    Residue on 20‑mesh sieve Sieve analysis (850 µm) % ≤2.0

    The resin is packaged in 25 kg multi‑wall paper bags with an inner polyethylene liner and demands storage at temperatures below 25°C and relative humidity below 60%. If the powder has been exposed to ambient humidity exceeding 70% RH, pre‑drying at 105°C for 2 hours (or fluidized‑bed drying at 80–90°C for 2–3 hours) is mandatory before melt processing to avoid bridging in hoppers and bubble‑induced gel defects in cast films.

    In suspension polymerization of vinyl chloride monomer (VCM), the water‑soluble protective colloid exerts dominant control over primary particle coalescence and the resulting PVC grain porosity. Sinopec PVA 098-45, charged at 0.05–0.30 phr relative to VCM, disperses monomer droplets under the turbulent shear field of a jacketed Hastelloy autoclave (typical capacity 70 m³, turbine impeller tip speed 6–9 m/s). The high degree of hydrolysis (> 98 mol%) depresses the critical micelle concentration and promotes rapid adsorption at the water/monomer interface, while the medium polymerization degree (DP ≈ 900) restricts solution viscosity to a regime that allows efficient shear transfer from the impeller without excessive viscous dampening. During the particle identity point, VCM graft polymerization onto the PVA backbone builds a steric barrier that suppresses catastrophic coalescence. Grafted layer density and interfacial rheology are markedly different from those generated by partially hydrolyzed PVA; this shifts the capillary number for drop breakup, allowing finer primary particle structure. Compared to high‑DP grades such as 2099 (DP 2000, viscosity 50–55 mPa·s), 098-45 yields a narrower particle size distribution and slightly lower internal porosity. PVC resin manufactured with 098-45 typically exhibits cold plasticizer absorption (per ASTM D3367) in the range 18–22 phr, whereas the same recipe using 2099 commonly reaches values above 25 phr. Published data for this specific configuration is limited; however, industrial experience confirms that the lower ash content of 098-45 (≤0.5% vs. ≤0.7% for 1799) reduces ionic conductivity in rigid PVC profiles, making it the preferred grade for medium‑voltage cable insulation compounds where the volume resistivity measured under IEC 60093 must exceed 10¹⁴ Ω·m. Pre‑drying the PVA powder to a moisture level <2.0% before addition to the VCM pre‑mix is critical to prevent foam nucleation that shifts the particle size distribution median toward <50 µm, generating excessive dust levels during resin drying.

    Why Does the Degree of Hydrolysis Dictate Water Resistance in Cold‑Water Soluble Films?

    Cast film produced from PVA 098-45 displays negligible mass loss when immersed in water at 20°C for 24 hours, a consequence of the dense intermolecular hydrogen‑bond network afforded by the high proportion of hydroxyl groups. Dissolution onset is registered only above 80°C under continuous agitation. This thermal barrier disqualifies the grade for unit‑dose detergent pods designed for cold‑wash cycles, where complete dissolution at 10–15°C is non‑negotiable; partially hydrolyzed grades such as Sinopec PVA 088-05 (hydrolysis 87–89 mol%, viscosity 4.0–6.0 mPa·s) are engineered precisely for that rapid cold‑water solubility. Nevertheless, 50 µm blown film manufactured from 098-45 affords outstanding resistance to methanol, toluene, and 10% sodium hydroxide solutions at ambient temperature, a property harnessed in hot‑filled agrochemical soluble sachets. Tensile strength tested per ISO 527‑3 at 23°C, 50% RH reaches 35–45 MPa with elongation at break 150–200%, versus 15–20 MPa for partially hydrolyzed films of equal gauge. The performance delta originates from the suppression of plasticizing water clusters in the fully saponified matrix, raising the glass‑transition temperature of the conditioned film by approximately 15°C relative to that of an 88 mol% hydrolyzed analogue.

    Warp Sizing on High‑Speed Looms: Penetration versus Film Integrity

    On modern air‑jet weaving units operating at weft insertion rates above 1500 m/min, the film‑forming binder in the size liquor must simultaneously penetrate the yarn interstices and yield a flexible, abrasion‑resistant surface coating. Formulations containing 6–8 wt% PVA 098-45 combined with modified corn starch and a hydrocarbon wax dispersion, applied on a multi‑cylinder sizing line (squeeze‑roller pressure 10–15 kN/m, drying cylinder surface temperature 120–130°C), produce a size film with a tensile strength of 28–32 MPa (ASTM D882) and an elongation at break of 120–150%. When substituted for high‑DP 1799 (film tensile strength > 45 MPa) in the identical formulation, 098-45 reduces yarn breakage per 100,000 picks by approximately 15% due to lower bending stiffness. The size add‑on required to achieve a satisfactory weaving efficiency declines from 10–12% to 8–9%, lowering subsequent desizing chemical demand. The medium‑viscosity profile of 098-45 also lessens the tendency to form skin‑over on the size‑box surface, a chronic defect when 2099 is processed at high solid contents.

    In paper coating applications, PVA 098-45 functions as a secondary binder alongside styrene‑butadiene latex. At an addition level of 2 parts per 100 parts pigment, the IGT pick velocity determined per ISO 3783 rises from 1.2 m/s (latex‑clay alone) to 1.8 m/s. The fully hydrolyzed structure resists rewetting during multi‑color offset printing, reducing blanket piling episodes by a factor of three in trials on a heatset web press operating at 12 m/s.

    When PVA 098-45 Replaces PVA 088-05 in Remoistenable Adhesive Formulations

    Envelope back‑gum and label remoistenable adhesives require instantaneous cold‑water tack development, a function served by partially hydrolyzed grades that dissolve in saliva or water at ambient temperature. PVA 098-45, being fully hydrolyzed, fails to generate the necessary open‑time tack at room temperature and is therefore excluded from remoistenable systems. Instead, the grade is deployed in heat‑seal adhesive coatings for carton closures and blister lamination where a hot‑knife activation temperature of 140–160°C fuses the film. The resulting bonded joint withstands immersion in cold water for more than 72 hours without delamination, a performance edge over 088‑05 joints that degrade within 2–3 hours. For tropical‑climate export packaging subjected to cyclic condensation under ISO 6270‑2, this constitutes a critical selection criterion.

    Cross‑Product Viscosity‑Hydrolysis Mapping: Selecting the Right PVA Grade

    Grade 4% aq. Viscosity (mPa·s) Hydrolysis (mol%) DP Ash (wt%) Volatile (wt%) Primary Application Domain
    098‑45 (2299) 45.0 ± 4.0 98.0–99.0 900 ± 50 ≤0.5 ≤5.0 Suspension PVC, hot‑water‑resistant films, heat‑seal adhesives
    1799 28–32 99.0–100 1700 ± 50 ≤0.7 ≤5.0 Textile warp sizing, paper surface strength, temporary protective films
    2099 50–55 99.0–100 2000 ± 100 ≤0.5 ≤5.0 High‑strength technical films, PVC suspension (co‑stabilizer), high‑load adhesives
    088‑05 5.0 ± 1.0 87–89 800 ± 50 ≤0.5 ≤5.0 Cold‑water soluble films (unit‑dose), remoistenable adhesives, dispersion stabilizer
    1788 22–28 87–89 1700 ± 50 ≤1.0 ≤5.0 Emulsion polymerization, pigment grinding, paper coating co‑binder

    The tabulated values are derived from manufacturer technical data sheets and represent lot‑typical figures under GB/T 12010 series methodologies. For applications demanding electrical purity, the ash content of 098‑45 (≤0.5%) places it on par with 2099 and substantially below 1788 (≤1.0%), an important factor when dielectric strength must exceed 20 kV/mm per IEC 60243‑1. Conversely, where cold‑water solubility is the first priority, 098‑45 must be rejected in favor of 088‑05 or 1788, but the penalty is a pronounced loss of film water resistance. The selection matrix therefore hinges on whether the process demands thermal activation or instant dissolution, with 098‑45 occupying the high‑resistance, hot‑activation niche.