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Anhui Liwei Chemical Co., Limited.

SELVOL Polyvinyl Alcohol 203

    • Product Name: SELVOL Polyvinyl Alcohol 203
    • 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 483426
    Product Name SELVOL Polyvinyl Alcohol 203
    Chemical Name Poly(vinyl alcohol)
    Cas Number 9002-89-5
    Appearance White granular powder
    Degree Of Hydrolysis 87.0 - 89.0 mol%
    Viscosity 4 Percent Solution At 20c 3.5 - 4.5 mPa·s
    Ph 4 Percent Solution 5.0 - 7.0
    Ash Content Max 0.5%
    Volatiles Max 5.0%
    Solubility Soluble in hot water, sparingly soluble in cold water
    Specific Gravity 1.19 - 1.31
    Bulk Density 0.4 - 0.6 g/cm³

    As an accredited SELVOL Polyvinyl Alcohol 203 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing SELVOL Polyvinyl Alcohol 203 is supplied in 25 kg multi-wall paper bags with polyethylene liner for protection.
    Container Loading (20′ FCL) 20′ FCL container loading: SELVOL Polyvinyl Alcohol 203 packed in bags on pallets, secured and protected for safe transit.
    Shipping SELVOL Polyvinyl Alcohol 203 ships as a solid powder in sealed, moisture-resistant bags or containers to prevent clumping and contamination. Keep dry, cool, and away from strong oxidizers during transit. Handle with clean equipment and protect packaging from tears. Non-hazardous under normal conditions, but avoid dust inhalation.
    Storage Store SELVOL Polyvinyl Alcohol 203 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and ignition sources. Keep containers tightly closed when not in use to prevent moisture absorption. Avoid exposure to high humidity and excessive temperatures, which can cause caking or degradation. Follow manufacturer’s shelf-life recommendations.
    Shelf Life Shelf life is typically 2 years from manufacture when stored in original, unopened containers under cool, dry conditions.
    Application of SELVOL Polyvinyl Alcohol 203

    At the partially hydrolyzed end of polyvinyl alcohol grades, SELVOL Polyvinyl Alcohol 203 is charged into vinyl acetate homopolymer and vinyl acetate-ethylene emulsion polymerizations as a protective colloid. The grade's nominal hydrolysis of 87–89 mol% and 4% aqueous solution viscosity of 3.5–4.5 mPa·s at 20 °C per ISO 2555 place it in the low-viscosity, moderate-residual-acetate class. During reactor start-up, the colloid solution is prepared at 90–95 °C under a high-speed dissolver until no gel particles remain. The solution is then metered into a jacketed semi-batch reactor at 2.0–5.0 wt% on total monomer. At the lower limit, particle stabilization becomes insufficient and coagulum is typically observed on the reactor wall and impeller when monomer conversion exceeds 60%. At the upper limit, final latex viscosity rises beyond the heat-transfer capability of a standard glass-lined reactor with a turbofoil impeller operating at 75–90 rpm. The 87–89 mol% hydrolysis level introduces residual acetate groups that reduce interfacial tension and favor grafting of vinyl acetate onto the PVOH backbone during the early particle nucleation stage. This grafted layer functions as the electrosteric barrier that limits shear-induced flocculation in high-speed dispersion units. For vinyl acetate-ethylene grades, SELVOL Polyvinyl Alcohol 203 permits an ethylene pressure of 1.5–4.0 MPa to be maintained without visible wax formation. Residual ethylene and vinyl acetate are stripped under vacuum; coagulum content is assessed after filtration through a 150 µm screen according to ISO 4576. The final latex typically exhibits a particle size of 0.2–1.5 µm and a solids content of 55–65 wt%, but exact values depend on the reactor's monomer feed profile and the ratio of delayed PVOH to initial charge. A process conflict exists when the same grade is used as the sole colloid in carboxylated styrene-acrylic systems: the partially hydrolyzed backbone may compete with monomer-soluble surfactants and reduce mechanical stability. Published data for this specific configuration is limited.

    What Role Does Low-Viscosity PVOH Play in PVAc White Glue?

    Because the low solution viscosity of SELVOL Polyvinyl Alcohol 203 permits high-solids PVAc compounding, the grade is used as a post-added stabilizer and rheology modifier at addition levels of 0.5–2.0 wt% of the finished adhesive. The low solution viscosity permits final adhesive viscosity adjustment to 5.0–12.0 Pa·s when measured by a Brookfield RVT spindle 6 at 20 rpm and 23 °C. Formulations compounded with this grade maintain acceptable spreadability on roller coaters and reduce stringing during transfer. Because the PVOH is partially hydrolyzed, the dried film retains some water sensitivity; adhesives predicated solely on SELVOL Polyvinyl Alcohol 203 do not meet EN 204 D3 water resistance without a crosslinking agent. Compounders add glyoxal at 0.5–2.0 wt% of the PVOH solids to convert free hydroxyl groups into acetal linkages and raise wet bond strength after the 4-day cold-water soak prescribed in EN 204. Under ASTM D905, shear strength on hard maple after conditioning at 23 °C and 50% relative humidity depends primarily on the PVAc dispersion, not on the small PVOH fraction. For indirect food-contact packaging, the formulation must comply with FDA 21 CFR 175.105; any crosslinker, plasticizer, and preservative must be cleared under the same section. Borate-containing preservatives or borax addition produce an immediate viscosity increase through diol complexation; this is avoided unless a thixotropic adhesive gel is explicitly targeted. Long-term storage at pH below 4.0 can hydrolyze the acetate groups in the polymer backbone and shift the adhesive rheology.

    When Aqueous Ceramic Slurries Require Burnout-Controlled Green Strength

    For dry-pressed tile bodies and technical ceramics produced from spray-dried granules, SELVOL Polyvinyl Alcohol 203 is added to aqueous slurries at 0.5–2.0 wt% of dry solids before spray drying. The low-viscosity profile allows slip total solids to be maintained at 65–72 wt% without exceeding the pressure nozzle viscosity limit, typically 500–800 mPa·s at 100 s-1. Green strength after pressing at 30–40 MPa is derived from PVOH bridges between particles. Overdosing above 2.0 wt% produces oversized spray-dried agglomerates and increases die wall friction. The grade's ash content, specified at a maximum of 0.5 wt% on the technical data sheet, is relevant because residual sodium acetate or other combustion by-products can contribute to black core if the kiln preheating zone is too short. Binder burnout in an oxidizing atmosphere completes between 400 °C and 500 °C, but full removal depends on granule size distribution and airflow. In fast-firing cycles below 35 minutes, incomplete burnout can leave carbonaceous residues that lower fired modulus of rupture under ISO 10545-4. Specific firing data for SELVOL Polyvinyl Alcohol 203 in porcelain tile compositions is limited; validation on a production spray dryer and kiln is required.

    Following size box application at 85–95 °C, SELVOL Polyvinyl Alcohol 203 is applied to cotton, viscose, and polyester-cotton warp yarns in combination with acid-thinned starch and an acrylic size. The bath solids are usually held at 6–10 wt%, with PVOH replacing 15–40 wt% of the starch fraction to improve yarn breaking strength and abrasion resistance. The low-viscosity grade reduces size box pickup variance on high-speed section warping, particularly when the size circulation loop is equipped with a heated storage tank and a pressure roll. Typical add-on after drying is 6–12 wt% on the dry yarn, confirmed by weighing a standard length of sized yarn against unsized yarn. Yarn tensile testing per ISO 2062 shows the largest relative benefit on carded cotton yarns, while polyester-cotton blends require the acrylic fraction to prevent film delamination. After weaving, the film is stripped in 80–90 °C water with 0.5–1.0 wt% wetting agent; bacterial amylase is added when starch content exceeds 50% of the total size solids. For 100% polyester filament warp sizing, SELVOL Polyvinyl Alcohol 203 is insufficient as a sole binder because the adhesion to the hydrophobic surface is too weak. An acrylic copolymer is required to meet loom abrasion requirements, and the PVOH fraction is retained only as a low-viscosity diluent for size bath stability.

    Paper Surface Sizing and Starch Extender Compatibility

    Surface sizing on corrugating medium and linerboard typically employs oxidized starch at 4–8 wt% solids in the size press; SELVOL Polyvinyl Alcohol 203 is incorporated at 0.3–1.5 wt% of dry starch to strengthen the starch film and reduce dusting. The grade's cold-water solubility and low viscosity permit direct addition to cooked starch at 50–60 °C without lump formation. Film split viscosity control on metering-size presses is improved because the PVOH does not contain insoluble shell particles that would leave blade streaks. Abrasion loss of the sized sheet, measured by TAPPI T 476, is reduced when the PVOH fraction is above 0.5 wt%. When water resistance is required, a glyoxal-based insolubilizer is used at 2–5 wt% on PVOH solids; otherwise the ISO 535 Cobb60 value remains high because the film is water-soluble. For food-contact paperboard, the surface sizing formulation must meet FDA 21 CFR 176.170 and FDA 21 CFR 176.180 or the applicable national equivalent. Paper machine runnability with this grade remains acceptable only when the return size is filtered through a 100 µm screen before re-entering the size press. At coat weights above 3.0 g/m² per side, the surface becomes tacky during drying at high moisture content and may require an after-dryer section above 120 °C.

    Casting Water-Soluble Films Without High-Molecular-Weight Blends

    In blown film lines, low-molecular-weight PVOH creates bubble instability, so SELVOL Polyvinyl Alcohol 203 is limited to cast film on release-coated belts. A solution of 10–15 wt% solids in water is heated to 85–95 °C and cast with a doctor blade gap of 0.3–0.8 mm. The partially hydrolyzed chemistry dissolves at lower temperature than fully hydrolyzed grades but provides lower melt strength. Compounding with higher-viscosity PVOH grades in the 20–50 mPa·s range at 4% concentration is necessary for blown water-soluble packaging films; published data for this specific SELVOL grade in blown film is limited. Tensile properties of cast film, measured by ASTM D638, depend on plasticizer type and content. Glycerol at 5–15 phr reduces film brittleness but also lowers the dissolution rate in 10 °C water. The partially hydrolyzed chemistry retains sufficient water solubility for quick-dissolving pouches, but the mechanical strength of a film cast exclusively from SELVOL Polyvinyl Alcohol 203 is generally below the threshold required for unit-dose detergent packaging. Manufacturers using this grade in water-soluble inserts typically blend it with a higher-viscosity partially hydrolyzed grade at 30:70 to 50:50 to balance castability and final tensile strength. Exact blend ratios are grade-specific and are validated on the converting line rather than derived solely from viscosity.

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    Certification & Compliance
    More Introduction

    SELVOL Polyvinyl Alcohol 203 is a partially hydrolyzed polyvinyl alcohol grade with a 4 wt% aqueous solution viscosity of 3.5–4.5 cP at 20 °C and a degree of hydrolysis of 87.0–89.0 mol% when tested according to JIS K6726. The product belongs to the lower-viscosity segment of the SELVOL portfolio and retains residual acetate functionality that reduces crystallinity, increases cold-water solubility, and moderates film stiffness relative to fully hydrolyzed equivalents. Release parameters include a pH of 4.5–6.5, volatile matter not exceeding 5.0 wt%, and ash expressed as Na₂O not exceeding 0.5 wt%. The grade is supplied as a granular powder and is selected for applications requiring water-sensitive adhesion, temporary sizing, or protective colloid performance without the higher viscosity contribution of medium-molecular-weight grades. In incoming quality-control practice, the 4 wt% solution viscosity is measured with a Brookfield rotational viscometer after complete dissolution and thermal equilibration; batches outside the 3.5–4.5 cP band are typically rejected before formulation. The partially hydrolyzed structure also lowers the dissolution temperature: dispersion at 25 °C is feasible with adequate agitation, whereas fully hydrolyzed grades require elevated temperature. This solubility boundary is a primary selection criterion in cold-water-dispersible adhesive, textile size, and paper sizing applications.

    What Separates Partially Hydrolyzed 203 from Fully Hydrolyzed 103 and Higher-Viscosity 205?

    The differentiation is based on two independent structural parameters: degree of hydrolysis and 4 wt% solution viscosity as an index of molecular weight. Table 1 summarizes comparative release ranges. SELVOL 103 matches 203 on viscosity but has a fully hydrolyzed structure, reducing cold-water solubility and producing stronger, less water-sensitive cast films. SELVOL 205 shares the partial hydrolysis range with 203 but contributes higher viscosity at equal solids. The practical consequence is that 203 offers the solubility advantage of partial hydrolysis without the viscosity penalty of higher-molecular-weight partially hydrolyzed grades. In dried film evaluations, ASTM D882 tensile measurements indicate that 203 develops lower tensile strength and higher elongation than 103 of equal 4 wt% solution viscosity; the difference is attributed to lower crystallinity and higher free volume. For remoistenable adhesives, the higher water sensitivity of 203 is an advantage, whereas for moisture-barrier coatings 103 or another fully hydrolyzed grade is preferred. Selection is therefore not an upgrade or downgrade but a shift in the solubility–mechanical property trade space.

    Comparative release ranges for SELVOL 103, 203, and 205
    ParameterSELVOL 103SELVOL 203SELVOL 205
    4 wt% aqueous viscosity at 20 °C3.5–4.5 cP3.5–4.5 cP5.2–6.2 cP
    Degree of hydrolysis98.0–98.8 mol%87.0–89.0 mol%87.0–89.0 mol%
    Cold-water solubility at 25 °CRequires heating to 80–90 °C for complete dissolutionSoluble with agitationSoluble with agitation; higher final viscosity
    Film moisture resistanceHigherLowerLower

    The table should not be interpreted as a direct one-to-one replacement guide. In applications where viscosity is the governing constraint, 203 can be substituted for 205 to reduce low-shear viscosity; in applications where film tensile strength and moisture resistance govern, 203 cannot replace 103 without reformulation. The exact viscosity reduction achieved depends on solids, co-solvents, and temperature; a Brookfield viscosity curve over solids is required before production substitution. SELVOL 203 also differs from medium-molecular-weight partially hydrolyzed grades such as 502 and from high-molecular-weight grades such as 540. A lower-viscosity grade is chosen when high-solids application is required at a given metering viscosity; a higher-viscosity grade is chosen when film build or thickening capacity is more important. In size press operation, pickup weight at fixed rod pressure is a function of low-shear viscosity; switching from a higher-viscosity grade to 203 can lower pickup unless solids are increased. The exact relationship is geometry-dependent and should be calibrated with a pilot size press or a production dilution series.

    Rheological Profile in 4 wt% Aqueous Solution and Solubility Boundary Conditions

    Solution preparation follows a hydration sequence. The powder is dispersed in cold water under low-shear propeller agitation, then heated to 60–80 °C for 30–60 min to complete hydration, and finally cooled to the use temperature. The resulting 4 wt% solution at 20 °C must fall within 3.5–4.5 cP by Brookfield rotational viscometer. At use concentrations above 10 wt%, heating and increased shear are required; below this concentration, cold-water swelling is generally sufficient. Operational boundaries include a pH of 4.5–6.5, which is compatible with stainless steel mixing vessels but does not provide preservative function; long-term solution storage can exhibit microbial viscosity drift unless a biocide is added. High ash content, controlled by the 0.5 wt% Na₂O maximum, influences film clarity; haze testing by ASTM D1003 can detect quality excursions. In melt-processing operations, the 5.0 wt% volatile matter maximum requires pre-drying to avoid feed throat blockage and hydrolysis in vented twin-screw extruders. The operational drying target is typically below 0.5 wt% moisture when 203 is used in water-soluble film extrusion.

    Viscosity stability over time is sensitive to solution temperature and agitation history. In sealed HDPE tanks at 25 °C, the low-shear viscosity can remain within 0.2 cP of the initial value for 72 h, but extended storage data for unpreserved solutions are limited. When stored at 4 °C, partially hydrolyzed solutions may develop slight haze; warming to 25 °C with gentle agitation restores clarity. These behaviors are measurable by Brookfield viscometry and visual inspection but do not indicate polymer degradation unless the pH drops below 4.0 or the solution develops a distinct acetic odor. High-shear dispersion above 1,000 rpm generates stable foam; defoamer is required in coating colors because foam increases apparent viscosity and causes pinholes in dried films. In size press operations, air entrainment is controlled by maintaining dissolved air below saturation and adding antifoam at 0.05–0.2 wt% on liquid. The exact antifoam dosage is determined by a foam cell test under standardized agitation.

    When 203 Replaces 205 in Paper Coating and Emulsion Polymerization Formulations

    In surface sizing and pigmented coating, 203 functions as a water-soluble binder and carrier colloid. At equal solids, a 203-based coating color exhibits lower Brookfield viscosity than a 205-based color because molecular weight, not hydrolysis, dominates low-shear viscosity. This can allow solids increases at constant metering viscosity; however, the high-shear capillary viscosity must be checked to avoid runnability defects on blade coaters. Substitution from 205 to 203 without adjusting solids can shift the coating color below the viscosity window required for stable metering and increase blade streaking if the high-shear viscosity falls too far. Pilot blade coater evaluations using a capillary viscometer at 10,000 s⁻¹ are required before production transfer; published data for this specific configuration is limited. A common transfer sequence is to prepare a solids ladder with 203 and measure both low-shear Brookfield viscosity and high-shear capillary viscosity, then adjust solids until the target application windows are matched.

    In emulsion polymerization of vinyl acetate and vinyl acetate-ethylene systems, 203 is charged in the aqueous phase as protective colloid at levels from 2–6 wt% on total monomer. The lower molecular weight reduces reactor viscosity and improves heat transfer in jacketed stirred reactors. Latex particle size and viscosity become less dependent on 203 than on higher-viscosity 205 at equal colloid loading, but colloidal stability may require higher addition levels of 203 to match the protective capacity of 205. Reaction temperature is typically maintained at 70–85 °C with pitched-blade turbine agitation. The exact colloid efficiency should be measured by latex particle size analysis and Brookfield viscosity at 25 °C. Because residual acetate groups affect colloidal stabilization and water resistance of the resulting dried film, the optimal colloid loading is system-specific; published data for high-solids vinyl acetate-ethylene copolymerization with 203 is limited.

    Adhesive applications use the water sensitivity of partially hydrolyzed 203. In remoistenable and water-activated tapes, the dry film re-wets rapidly at 25 °C; the low viscosity permits high-solids formulations without excessive viscosity. For paper tube winding and lamination adhesives, 203 is combined with plasticizers and fillers; open time and tack are influenced by solids, not only by grade selection. In textile warp sizing, 203 is formulated at 4–8 wt% solids for filament or staple yarns on single-size-box slashers. The dried size film must balance tensile protection during weaving with complete removal in desizing baths at 50–70 °C; partially hydrolyzed grades such as 203 desize more readily than fully hydrolyzed 103 because of higher cold-water swelling. Production-scale desizing efficiency is typically checked by residual starch/polyvinyl alcohol detection after the wash boxes; published data for this specific configuration is limited.

    Regulatory assessments for indirect food contact should be based on the specific formulation and service conditions. Polyvinyl alcohol may be evaluated under 21 CFR 175.105 for adhesives and 21 CFR 176.170 for paper and paperboard components; compliance cannot be inferred from the polymer grade alone. The grade should not be combined with strong oxidizing agents or certain borates in aqueous systems because gelation or precipitation can occur; the pH range of 4.5–6.5 also indicates that addition of strong acids or bases can accelerate acetate hydrolysis and shift solubility. In powder handling, dust control is required to avoid combustible dust atmospheres; the product should be stored dry and away from open flame. At relative humidity above 60 %, the granular powder adsorbs atmospheric moisture, and the 5.0 wt% volatile matter limit may be exceeded unless storage silos are purged with dry air.

    Selected standard test methods applicable to SELVOL Polyvinyl Alcohol 203 release and application evaluation
    PropertyMethodCondition
    4 wt% aqueous viscosityJIS K6726Brookfield rotational viscometer at 20 °C
    Degree of hydrolysisJIS K6726Saponification titration
    Volatile matterJIS K6726Drying at 105 °C to constant weight
    Ash as Na₂OJIS K6726Ignition at 800 °C
    Film hazeASTM D1003Cast film, 0.1 mm dry thickness
    Film tensile propertiesASTM D882Cast film, 23 °C, 50 % RH