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Anhui Liwei Chemical Co., Limited.

KURARAY POVAL 30-88

    • Nombre del producto: KURARAY POVAL 30-88
    • Sitio de fábrica: Lingwu, Yinchuan, Ningxia, China
    • Consulta de precio: sales2@liwei-chem.com
    • Fabricante: Anhui Liwei Chemical Co., Limited.
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    Especificaciones
    Código HS 138820
    Nombre Químico Poli (alcohol de vinilo)
    Cas Número 9002-89-5
    Apariencia Polvo granular blanco a amarillo pálido
    Viscosidad 4 Por Ciento Solución 20c Mpa S 28-32
    Grado De Hidrólisis Mol Por Ciento 87-89
    Solución Acuosa De Ph 5-7
    Densidad G Cm3 1,27
    Solubilidad Soluble en agua caliente; ligeramente soluble en agua fría
    Punto De Fusión C ~ 200 (se descompone)
    Temperatura De Transición Vítrea En C ~ 75

    Como fábrica acreditada KURARAY POVAL 30-88, hacemos cumplir estrictos protocolos de calidad: cada lote se somete a rigurosas pruebas para garantizar estándares consistentes de eficacia y seguridad.

    Embalaje y almacenamiento
    Embalaje Kuraray Poval 30-88 está empaquetado en bolsas de papel de pared múltiple de 25 kg con un revestimiento de polietileno para una protección segura.
    Carga De Contenedores (20 'FCL) 20 'FCL: KURARAY POVAL 30-88 cargado como bolsas paletizadas, envueltas en plástico retráctil, con protección contra la humedad, con refuerzo seguro para evitar daños y contaminación.
    Envío KURARAY POVAL 30-88 (alcohol polivinílico) se envía como una resina granular seca y soluble en agua en papel de múltiples paredes sellado o bolsas forradas de PE, típicamente paletizadas y envueltas elásticas para protección. No está clasificado como mercancía peligrosa, pero debe mantenerse seco, lejos de la humedad, el calor y las fuentes de ignición, con medidas estándar de control de polvo durante el manejo.
    Almacenamiento Guarde KURARAY POVAL 30-88 (alcohol polivinílico) en un área fresca, seca y bien ventilada, lejos del calor, fuentes de ignición, humedad y oxidantes incompatibles. Mantenga el recipiente original herméticamente cerrado cuando no esté en uso para evitar la absorción de humedad y la contaminación. Evite condiciones que generen polvo en el aire o descarga estática. Garantice un etiquetado adecuado y sepárelo de los alimentos.
    Duración La vida útil es típicamente de 24 meses desde la fabricación cuando se almacena en contenedores originales sellados en condiciones frías y secas.
    Aplicación de KURARAY POVAL 30-88

    Which Hydrolysis Level Controls Grafting Density in Vinyl Acetate Emulsion Polymerization?

    In semi-batch vinyl acetate homopolymerization, the 87–89 mol% hydrolysis range of Kuraray Poval 30-88 is not a passive specification; the residual 11–13 mol% acetyl groups function as radical transfer and grafting sites during persulfate initiation, forming the interfacial polyvinyl alcohol-polyvinyl acetate layer that regulates emulsion particle size and shelf stability. The grade is dissolved in demineralized water at 85–90 °C for 30–45 min at 4.0–6.0% solids, cooled to 70–75 °C, and charged into a 3,000–5,000 L glass-lined or stainless reactor equipped with an anchor agitator running at 80–120 rpm. The protective colloid addition is 3.0–5.0 wt% based on total vinyl acetate monomer, while potassium persulfate initiator is fed separately at 0.15–0.30 wt% on monomer after the initial charge reaches 68 °C. Monomer is metered over 3.5–4.5 h with the reaction band held at 65–75 °C. Production operators monitor agitator torque and jacket heat transfer; a torque rise above 85% of motor rating indicates particle aggregation, and the monomer feed is reduced by 5–10% while 0.05 wt% sodium acetate buffer is added to return the batch pH to 4.5–5.5. The resulting polyvinyl acetate dispersion typically contains 50–55% solids, Brookfield viscosity of 8,000–20,000 mPa·s at 25 °C, and a particle size D50 of 0.6–1.8 μm. Batch-to-batch variation in the incoming 4% solution viscosity of 30-88, specified at 27.0–33.0 mPa·s, can shift final dispersion viscosity by approximately ±10% at equivalent solids. Compliance for the unmodified dispersion falls under FDA 21 CFR 175.105 for indirect food-contact adhesives, while paperboard applications are assessed under 21 CFR 176.170. Terminal products include white woodworking PVAc glue, paper tube adhesive, bookbinding emulsion, and general lamination adhesive. Operational boundary: 30-88 alone does not achieve a D4 water-resistant bond under EN 204; a crosslinker is required when that classification is specified.

    On a flooded nip size press running at 800–1,100 m/min, the surface sizing liquor is formulated with oxidized starch and 30-88 at a dry ratio of 70:30 to 60:40, with total bath solids maintained between 6.0–8.0%. The PVA component is pre-dissolved at 90–95 °C for 45 min and blended with starch at 55–60 °C to avoid retrogradation. Film press pickup is controlled to 1.0–2.5 g/m² per side through nip pressure of 40–80 kN/m; after application, the web passes through infrared dryers and cylinder sections with surface temperatures from 90 °C to 120 °C, with final moisture held at 5.0–6.0%. The 88 mol% hydrolysis level of 30-88 reduces water absorption while preserving film flexibility, a required balance for high-speed converting. Compliance is verified with ISO 535 Cobb60, TAPPI T 530 Hercules sizing test, and ISO 5627 Bendtsen roughness; food-contact grades are cleared under 21 CFR 176.170 and 21 CFR 176.180. Terminal product types include high-speed inkjet coated paper, offset printing base stock, silicone release liner base, and direct thermal paper base. Operational limitation: at relative humidity above 65%, size press pickup drifts because the reeled paper enters with higher moisture, so the web must be pre-dried to 3.0–4.5% moisture before the size press.

    Application variable30-88 sizing windowTest method
    Size press bath solids6.0–8.0%Oven solids
    PVA-to-starch dry ratio30:70–40:60Mass balance
    Pickup per side1.0–2.5 g/m²ISO 536 basis weight differential
    Water absorptiveness20–40 g/m² Cobb60ISO 535
    Sizing holdout20–150 s HSTTAPPI T 530

    Warp Sizing Viscosity Stability in Air-Jet Weaving Sheds

    Size box viscosity drift is controlled when 30-88 is blended at 35–50% of total size solids with native or modified starch, at total solids of 9.0–13.0%. The liquor is cooked at 120–130 °C in a jet cooker for 10–15 min and held at 75–80 °C in the size box of a single-end slasher processing 7.4–9.8 tex ring-spun polyester/cotton warp yarn. Squeeze pressure is maintained at 140–220 kN/m to achieve 8.0–12.0 wt% add-on; drying cylinder temperatures are zoned at 90 °C, 125 °C, and 110 °C, with warp moisture at lease controlled to 4.0–6.0%. The sized warp is woven on air-jet looms at 800–1,200 rpm. The film formed by 30-88 reduces protruding fiber and stiffening without excessive shedding in the shed. After weaving, the fabric is desized in open-width washers at 80–95 °C with 0.5–1.0 g/L wetting agent and 10–20 min residence; residual PVA in effluent is measured by ISO 6060 chemical oxygen demand. Compliance for the input chemical includes OEKO-TEX Standard 100 product class II where finished fabric is certified; discharge limits are site-specific, but residual PVA contributes to COD and must be accounted for in the mill wastewater permit. Terminal finished products are air-jet woven denim, workwear shirting, and bed linen base fabric. The main incompatibility is with cationic size additives and strong acid desizing agents; combination with alum below pH 4.0 causes gelation and size bath instability.

    Where remoistenable front-seal adhesives must survive 12 months of warehouse cycling between 15 °C and 40 °C at up to 75% RH, 30-88 is compounded at 25–40 parts per 100 parts dry adhesive solids with oxidized dextrin or thin-boiling starch, and plasticized with 5–10 parts glycerol per 100 parts PVA. The batch is dispersed in water at 30–35% solids, cooked at 85–90 °C, and applied by a 110–150 line/cm gravure cylinder at 8–15 g/m² wet film to the paper substrate. A 3-zone forced-air oven set at 60 °C, 75 °C, and 85 °C dries the coating in 5–8 s, followed by conditioning to 45–55% RH before slitting. The rewetting response on automated inserting lines is targeted at 2–5 s open time with 0.2–0.5 mL water per seal. Compliance for indirect food-contact envelopes and label patches is covered under FDA 21 CFR 175.105; EU paper packaging falls under Regulation (EC) 1935/2004 with good manufacturing practice under Regulation (EC) 2023/2006. Terminal types include self-seal envelopes, stamp mounts, direct mail label patches, and wallpaper joint tapes. 30-88 is not recommended for direct food-contact application and is not a cold-water-instant dissolution grade; dissolution requires heating to 85–90 °C during adhesive compounding.

    When 30-88 Replaces Fully Hydrolyzed Grades in Ceramic Extrusion Binder Systems

    Alumina and cordierite honeycomb bodies respond differently to the 88 mol% hydrolysis level because residual acetate groups lower the binder solution gel point and alter pressure drop through extrusion dies. 30-88 is pre-dissolved at 15–20% solids in deionized water at 85–90 °C, then added to the ceramic batch at 1.0–2.5 wt% dry basis with 2.0–4.0 wt% polyethylene glycol plasticizer and 0.5–1.0 wt% stearic acid lubricant. Mixing is carried out in a sigma-blade kneader to a plastic body moisture of 16–20%. Extrusion through 300–600 cell/in² honeycomb dies occurs at head pressure 20–35 bar and body temperature 25–35 °C. Green ware is dried at 40–60 °C to residual moisture 0.5–1.0%, then debindered at 450–550 °C with 2–4 h hold and air flow 1.0–1.5 m/s to keep carbon residue below 0.1%. The ash specification for 30-88 is <0.5%, which is critical for high-purity alumina substrates. Terminal products include automotive catalyst honeycomb substrates, diesel particulate filter segments, and kiln furniture. Compliance is process-specific: ceramic bodies are usually qualified under ISO 9001 production controls, while fired parts may be tested to ASTM C373 for water absorption; no food-contact migration standard applies to the organic binder because it is removed by firing. Operational boundary: at body moisture above 21%, laminations form during extrusion, and below 15%, die pressure exceeds 35 bar and causes wear on coated dies.

    Crosslinker Consumption Rises When 30-88 Replaces 98 mol% Grades in Laminating Adhesives

    After 24 h of cure at 20–25 °C and 50% RH, a two-part polyvinyl acetate laminating adhesive containing 2.5–5.0 wt% 30-88 solids develops water-resistant bonds to paper-foil and paper-film structures. The 30-88 stock solution is mixed into the PVAc dispersion at 15–20% solids, and an acid-catalyzed crosslinker such as glyoxal or a blocked isocyanate is added at 0.5–1.5 wt% on total wet adhesive. Roller coating applies 40–80 g/m² wet to the paper or foil web, followed by nip pressure 3–6 bar, tunnel drying at 70–90 °C for 20–40 s, and re-moistening on a gravure station before lamination. The 30-88 component increases cohesional strength, but because 88 mol% hydrolysis leaves 11–13 mol% acetyl groups, hydroxyl availability for crosslinking is lower than in fully hydrolyzed grades; above 5.0 wt% 30-88 the wet adhesive viscosity rises above 20,000 mPa·s and working time drops below 2 h. Compliance for food packaging laminates is evaluated under FDA 21 CFR 175.105, EU Regulation 10/2011, and EN 204 D3 where wood-composite claims are involved. Bond performance is tested with ASTM D1876 T-peel and ASTM D3985 oxygen transmission after 7 days conditioning. Terminal products are paper-polyethylene foil pouches, aluminum-foil barrier wraps, and multi-layer label backings. Incompatibility: combination with amine-catalyzed epoxy hardeners at pH above 8.5 leads to premature gelation; pH is maintained between 4.5 and 5.5 during mixing.

    Compliance referenceScopeMeasured property
    FDA 21 CFR 175.105Indirect food-contact adhesiveFormulation limits
    EU Regulation 10/2011Food-contact plastic layersOverall migration 10 mg/dm²
    ASTM D1876T-peel resistancePeel strength N/25 mm
    ASTM D3985Oxygen transmissioncm³/(m²·day·bar)
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    Certificación y cumplimiento
    Más Introducción
    Kuraray POVAL 30-88 is a partially hydrolysed polyvinyl alcohol grade defined by two primary specifications: a nominal 4% aqueous solution viscosity of 30 mPa·s at 20°C and a nominal degree of hydrolysis of 88 mol%. The product is supplied as a white to off-white granular powder that is soluble in hot water; it is not cold-water soluble at 25°C. Under JIS K6726:1994, the control ranges typically presented for this grade include a viscosity of 27.0–33.0 mPa·s, a hydrolysis level of 87.0–89.0 mol%, volatile matter not exceeding 5.0%, ash as Na₂O not exceeding 0.5%, and a pH between 5.0 and 7.0 for a 4% solution. The combination of moderate chain length and partial hydrolysis places the material between low-viscosity surface-active PVOH grades and high-viscosity fully hydrolysed grades. Residual acetate groups depress crystallinity and reduce the energy required for dissolution relative to a 98–99 mol% hydrolysed grade, while the 88 mol% hydroxyl content retains sufficient interchain hydrogen bonding to form a coherent cast or coated film after drying.
    Property Typical value Test basis
    Degree of hydrolysis 87.0–89.0 mol% JIS K6726:1994
    Viscosity of 4% aqueous solution 27.0–33.0 mPa·s at 20°C JIS K6726:1994
    Volatile matter ≤ 5.0% JIS K6726:1994
    Ash as Na₂O ≤ 0.5% JIS K6726:1994
    pH of 4% solution 5.0–7.0 JIS K6726:1994
    In solution preparation, the solid is typically introduced through a low-shear eductor or centrifugal sifter into a jacketed stainless steel vessel containing water at 85–90°C. If dry powder is dumped directly into a high-speed vortex without sifting, hydrated gel layers form around undissolved cores, producing fish-eye defects that can persist through 150 μm filters. For incoming inspection, viscosity testing alone is not sufficient to detect low-level crosslinked gels. A typical quality control protocol includes visual inspection of a 10% solution after passing through a 150 μm sieve, with gel particle counts reported as number per 100 g of solid. The alcoholysis degree is verified by saponification value; residual acetyl content may also be measured by hydrolysis and titration.

    How Do Molecular Weight and Residual Acetate Distribution Influence Solubility and Film Tensile Response?

    The prefix “30” indicates a longer average chain length than grades such as 22-88 or 5-88. At equal hydrolysis, higher molecular weight raises the viscosity of a 4% solution and increases extensional viscosity in the film split during roll application. In a 5,000 L jacketed dissolution vessel with a bottom-mounted axial-flow impeller running at 40–60 rpm, a 10 wt% batch is normally fully dissolved in 90–150 min at 85°C. If the heating ramp is shortened or the vessel is operated below 80°C, residual gel particles can be carried downstream and appear as streaks in a subsequent coating nip. The 88 mol% hydrolysis level also controls solubility and film properties. Fully hydrolysed PVOH requires holding temperatures above 90°C and longer swelling times because dense hydrogen-bonded crystalline domains resist water ingress. In 30-88, randomly distributed acetate groups interrupt crystallite growth and allow a lower dissolution temperature, but they also reduce ultimate water resistance of the dried film. A dried film formed from 30-88 will exhibit measurable swelling and softening in cold water, whereas a fully hydrolysed grade remains intact until hot water is applied. Tensile testing of cast films under ASTM D882-18 typically shows that 30-88 films are more extensible than fully hydrolysed PVOH and stronger than 5-88 films at equal plasticiser content. Published data for specific plasticiser formulations is limited; observed industrial behaviour varies with plasticiser type and drying temperature. Where 30-88 is used as a protective colloid in vinyl acetate emulsion polymerization, the addition level is commonly 3.0–3.5 wt% on total monomer. In a 500–1,000 L glass-lined reactor with a pitched-blade turbine at 80–120 rpm, the colloid stabilises growing latex particles and reduces coagulum build-up on the vessel wall. The residual acetate groups participate in radical grafting to the PVOH backbone; this grafting alters the stabiliser layer and produces pseudo-plastic flow in the finished latex. Increasing the PVOH fraction from 3.0 wt% to 5.0 wt% raises low-shear Brookfield viscosity at 20 rpm and may shift the particle size distribution measured by laser diffraction toward larger mean diameters. Scale-up from laboratory glassware to a 1,000 L reactor is not linear. The lower surface-to-volume ratio changes heat removal, and persulfate initiator addition must be ramped accordingly. If the exotherm is not controlled within ±2°C, grafting density changes and batch-to-batch low-shear viscosity can vary by more than 20%. At comparable addition levels, 30-88 produces higher latex viscosity and better wet-tack than 5-88 because the longer chains bridge adjacent particles more effectively. However, the increased low-shear viscosity can complicate handling in high-solids formulations; pumps, filters, and filling lines must be sized for shear-thinning behaviour. Rheological evaluation under ISO 3219:1993 or DIN 53019-1:2008 is recommended when shifting from a low-viscosity grade to 30-88.

    Grade-Differentiating Properties in Aqueous Adhesive and Barrier Coating Applications

    In paper surface sizing, a 6.0–8.0% solids solution of 30-88 maintained at 70–80°C on a film press can deposit dry coat weights of 3–5 g/m² when metered with a rod or smooth-roll applicator. The grade’s viscosity contributes to a stable film split and reduces spattering compared with lower-molecular-weight PVOH, but the solids window narrows above 9.0% because the solution can become too viscous for uniform transfer at 600 m/min line speeds. Surface strength is often assessed via ISO 3783 IGT pick resistance; comparative trials show that PVOH addition at 3.0–5.0% of coating solids improves dry pick resistance, while wet pick resistance depends on the cure of the co-binder and the base-sheet internal size. Aqueous adhesive formulations exploit similar film-formation and colloidal stabilisation behaviour. In remoistenable adhesives, 30-88 can be compounded with plasticisers and defoamers; the higher molecular weight increases bond strength relative to 22-88 but raises the viscosity of a 20% solids formulation. Formulators typically dilute by 2–5% additional water when transitioning from 22-88 to 30-88 to maintain identical coating viscosity.
    Grade Nominal 4% viscosity at 20°C (mPa·s) Nominal degree of hydrolysis (mol%) Processing consequence in aqueous formulation
    POVAL 30-88 30 88 Higher film cohesion than 22-88 at equal solids; requires heating to 80–85°C
    POVAL 22-88 22 88 Lower viscosity at equal solids; reduced wet pickup on cylinder presses
    POVAL 5-88 5 88 Easier cold-water handling; lower tensile strength of cast film
    Fully hydrolysed PVOH 27–33 98–99 Higher water resistance after drying; dissolution above 90°C
    On textile warp sizing lines processing polyester–cotton blends, a 10–13% solids solution of 30-88 is applied in size boxes at 75–85°C. The higher viscosity of the grade provides adequate size add-on at squeeze pressures of 0.3–0.5 MPa on a two-roll padder, reducing the need for high add-on from low-viscosity grades. Desizing is carried out with hot-water washing at 80°C because the size film must be removed before dyeing; the partially hydrolysed PVOH re-dissolves more readily than fully hydrolysed size, but is not removable in cold water. Yarn tensile strength retention after sizing is typically evaluated under ISO 2062:2009; the PVOH film increases abrasion resistance during weaving as measured by loom stop counts per 100,000 picks. Published data for specific weave-room stop counts is formulation-dependent and limited.

    When a Low-Moisture Melt Process Replaces Hot-Water Solution Preparation

    Partially hydrolysed PVOH is not commonly processed as a neat melt because the temperature window between flow initiation and thermal degradation is narrow. For 30-88, the crystalline melting range is below that of fully hydrolysed PVOH, but thermal degradation accelerates above 200°C. If a twin-screw compounding line is selected, plasticiser incorporation of 15–30 phr is required to bring the melt temperature into a processable range. In a co-rotating twin-screw extruder with an L/D ratio of 40:1, a barrel temperature profile from 90–170°C and a die temperature below 180°C can be used for plasticised formulations. Without sufficient plasticiser, shear heating in the kneading blocks raises the melt temperature above 200°C, producing yellowing, generation of acetic acid, and gel formation. These observations are consistent with the known thermal degradation pathway of PVOH, but published data for this specific melt-processing configuration is limited. Aqueous solution processing remains the standard route for 30-88 in high-volume coating lines. Regulatory data sheets for Kuraray POVAL 30-88 list the substance as polyvinyl alcohol under CAS 9002-89-5. Under REACH, the grade is registered as a polymer, and exposure controls address dust containment rather than acute toxicity. For food-contact use, polyvinyl alcohol films and coatings may be evaluated under FDA 21 CFR 177.1670 or 21 CFR 175.300 depending on the final article; end-use migration testing is required because the grade itself does not establish compliance limits. Storage should be in sealed bags at relative humidity below 60% and below 30°C. Moisture uptake above 60% RH increases caking and can alter gravimetric feeding; pneumatic transfer lines should be designed for a bulk density near 0.40–0.60 g/cm³, but the exact packed density depends on particle-size distribution and consolidation. In aqueous formulation, 30-88 should be protected from strong oxidizing agents and from excessive alkaline hydrolysis at pH above 10 during prolonged hot storage. Addition of borate salts at even 0.1% by weight can produce reversible but high low-shear viscosity increases through borate-diol complexation; crosslinked gels can block filters and coating lines. These incompatibility boundaries are reversible under acidic pH adjustment but are difficult to reverse once films are dried.