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Anhui Liwei Chemical Co., Limited.

KURARAY POVAL 20-98 M

    • Product Name: KURARAY POVAL 20-98 M
    • 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 460208
    Product Name KURARAY POVAL 20-98 M
    Chemical Type Polyvinyl alcohol
    Physical Form White powder or granules
    Viscosity 4pct Aqueous Solution At 20c 20.0 - 26.0 mPa·s
    Hydrolysis Degree 98.0 - 99.0 mol%
    Ph 4pct Aqueous Solution 5.0 - 7.0
    Ash Content ≤ 0.5 wt%
    Volatile Content ≤ 5.0 wt%
    Average Polymerization Degree 2000
    Average Molecular Weight 88000 g/mol
    Density 1.27 - 1.31 g/cm³
    Melting Point 200°C
    Tensile Strength 50 - 70 MPa
    Elongation At Break 15 - 30%

    As an accredited KURARAY POVAL 20-98 M factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Kuraray Poval 20-98 M is supplied as granules in 20 kg multilayer paper bags, palletized and shrink-wrapped.
    Container Loading (20′ FCL) Kuraray Poval 20-98 M loaded in 20ft FCL: 25kg bags on pallets, shrink-wrapped, evenly distributed, dry, ventilated, securely braced.
    Shipping KURARAY POVAL 20-98 M is a polyvinyl alcohol powder shipped in sealed multi-layer paper or PE-lined bags, palletized and stretch-wrapped. It is non-hazardous for transport, but should be kept dry and protected from moisture. Avoid direct heat, and handle with standard dust-control precautions during unloading.
    Storage Store KURARAY POVAL 20-98 M in a cool, dry, well-ventilated area away from heat, open flames, and direct sunlight. Keep the original container tightly sealed to prevent moisture absorption and contamination. Avoid dust accumulation and static discharge. Maintain moderate humidity, and use within the manufacturer’s recommended shelf life.
    Shelf Life Shelf life is typically two years from production when stored sealed in a cool, dry place.
    Application of KURARAY POVAL 20-98 M

    Kuraray POVAL 20-98 M is supplied as a fully hydrolyzed polyvinyl alcohol powder with a 4% aqueous solution viscosity of 20.0–22.0 mPa·s at 20 °C and a degree of hydrolysis of 98.0–99.0 mol% measured in accordance with JIS K6726. In paper surface sizing and pigment coating, the grade is used where low cold-water sensitivity and high dry pick resistance must be maintained on lithographic and packaging grades. The resin is dispersed in cold water at ambient temperature, then heated to 90–95 °C for 30–45 min in a jet cooker or agitated jacketed tank to complete dissolution; the solution is cooled to 55–65 °C and held. Typical surface size formulations add 10–30 dry parts of 20-98 M per 100 dry parts of total size solids, with the balance oxidized starch or a starch/polyacrylamide blend, depending on the target Hercules size test response. Application on a metering size press or rod-metering film press deposits 0.8–2.5 g/m² per side. Sizing response is quantified by TAPPI T 530 on the Hercules scale and water absorption by ISO 535 Cobb testing. The fully hydrolyzed backbone reduces the binder contribution to Cobb value and improves IGT dry pick strength relative to partially hydrolyzed 88 mol% grades. Terminal products include recycled white-top liner, folding boxboard, and sheet-fed offset packaging. Food-contact compliance is established under FDA 21 CFR 176.170 for aqueous and fatty food-contact paper and FDA 21 CFR 176.180 for dry food-contact paper; the substance is registered under REACH Regulation 1907/2006. Process boundaries include foam in high-shear hold tanks using centrifugal size pumps with recirculation above 15 tank turnovers/h, which requires a defoamer dose of 0.05–0.15 wt% based on wet size solution. The polymer is incompatible with borate-containing additives, which cause gelation; blending pH should remain above 5.0.

    Regulatory referenceScopeUse condition
    FDA 21 CFR 176.170Paper and paperboard for aqueous and fatty food contactSurface sizing and pigment coating at GMP
    FDA 21 CFR 176.180Paper and paperboard for dry food contactSurface sizing and pigment coating at GMP
    FDA 21 CFR 175.105Adhesives for indirect food contactRemoistenable adhesives at GMP
    REACH Regulation 1907/2006Substance registration and restrictionsRegistered; no Annex XVII restriction for PVOH
    JIS K6726PVOH analytical specificationViscosity and hydrolysis degree lot certification

    What Controls Remoistenable Adhesive Wet Tack on High-Speed Envelope Converting Lines?

    Remoistenable gum systems formulated with Kuraray POVAL 20-98 M are processed as aqueous solutions at 25–45 wt% dry solids and applied to envelope flaps, paper sacks, labels, and stamps by engraved roll or transfer coater. The fully hydrolyzed grade yields a dry film that remains non-tacky at ambient humidity and develops adhesion only after controlled remoistening; this behavior reduces feed table blocking on high-speed window-patching lines. A typical formulation combines 100 dry parts of 20-98 M with 30–60 dry parts of dextrin or thin-boiling starch, 5–15 phr of glycerol or sorbitol as plasticizer, and 0.1–0.3 phr of defoamer. The adhesive is cooked at 85–95 °C and applied at 50–65 °C through an engraved coater or kiss coater onto gummed areas. Wet coat weight ranges from 5–20 g/m², followed by forced-air drying at 60–90 °C to residual moisture below 5.0 mass%. Peel adhesion after remoistening with 10–15 g/m² of water is evaluated by ASTM D903. Blocking resistance is screened by stacking finished envelopes at 40 °C and 70 % relative humidity for 72 h under 5–10 kPa load. The main operational boundary is humidity exposure above 70 %; blocking may occur unless anti-block additives such as calcium stearate at 0.5–1.0 phr are added. Borax or boric acid must not be added above trace amounts because these crosslink the fully hydrolyzed PVOH and produce irreversible gelation in the holding tank. The dried adhesive is compliant with FDA 21 CFR 175.105 for indirect food-contact adhesives when applied under good manufacturing practice. Terminal articles include self-seal envelopes, remoistenable wallpaper borders, and high-speed insertion mailers.

    In aqueous ceramic tape casting, Kuraray POVAL 20-98 M functions as a fully hydrolyzed binder for alumina, zirconia, barium titanate, and low-temperature co-fired ceramic formulations. A binder solution is prepared separately at 10–15 wt% solids by heating to 90 °C, then cooled before addition to the slip to avoid flocculation. The ceramic slip is milled with deionized water, ammonium polyacrylate dispersant at 0.5–1.5 wt% based on ceramic powder, defoamer at 0.1–0.3 wt%, and plasticizer such as PEG 400 at 10–30 wt% based on polymer. Binder addition is expressed as 2–6 dry parts per 100 dry parts ceramic powder; the final slip solids are typically 55–75 wt%. Viscosity is controlled to 1500–4000 mPa·s at 10 s⁻¹ using a cone-plate rotational rheometer. After vacuum de-airing at 20–50 kPa for 10–20 min, the slip is cast onto a polyethylene terephthalate carrier with a doctor blade gap of 0.25–0.60 mm. Carrier speed is set between 0.3 and 1.5 m/min, and drying is carried out in a segmented tunnel at 50–80 °C until residual moisture falls below 1.0 mass%. Green tapes of 0.10–0.35 mm thickness are laminated at 10–20 MPa and 70 °C for multilayer builds. Binder burnout in air uses a ramp rate no greater than 0.5 °C/min through 550 °C, with isothermal holds at 150 °C, 350 °C, and 600 °C to prevent blistering and residual carbon defects. Resin ash is specified below 0.5 mass% after incineration at 900 °C according to ISO 3451-1. Sintered substrates are checked for water absorption and apparent porosity under ASTM C373. The grade is suitable for multilayer ceramic capacitor green sheet, LTCC modules, oxygen sensor substrates, and ceramic heater plates. Operational limits include slurry pot life of 24–48 h without biocide addition, because PVOH solutions support microbial growth; processing above 48 h requires a preservative compatible with the ceramic dispersant. Binder contents above 6 dry parts per 100 dry parts powder increase green strength but lengthen burnout and raise residual carbon risk in reducing atmospheres.

    Fully Hydrolyzed PVOH Feedstock Provides the Backbone for Butyralization

    The butyralization reactor charge is prepared by dissolving Kuraray POVAL 20-98 M in demineralized water at 90–95 °C to 8–12 wt%, then cooling to 20–40 °C before catalyst addition. Butyraldehyde is added at 0.7–0.9 mol per mole of vinyl alcohol unit, and hydrochloric or sulfuric acid drops the pH to 1.5–2.5. Precipitation of polyvinyl butyral occurs as the reaction proceeds through 3–6 h; the precipitated resin is washed repeatedly until residual ionic impurities are below lot specification by ion chromatography. The 20-98 M grade at 20.0–22.0 mPa·s delivers a lower molecular weight fully hydrolyzed backbone than higher-viscosity PVOH grades, which reduces melt viscosity during subsequent sheet extrusion and permits faster line speeds on 0.76 mm and 1.52 mm interlayer calenders. Typical PVB resin after butyralization contains 75–80 mol% butyral units, 15–20 mol% residual hydroxyl, and less than 1.5 mol% residual acetate. Compounding with plasticizer at 25–40 phr is followed by extrusion through a flat die at 180–220 °C. Laminated glass made from the interlayer is tested under ISO 12543 and, for automotive glazing, ECE R43. The terminal product is safety glass for architectural and automotive applications. Processing boundaries are set by the relationship between residual hydroxyl and adhesion: hydroxyl content below 15 mol% reduces glass adhesion in pummel testing, while content above 20 mol% increases moisture sensitivity of the interlayer. The use of a fully hydrolyzed PVOH feedstock rather than an 88 mol% grade raises crystal density in the dry polymer, requiring the dissolution stage to be held at or above 90 °C; incomplete dissolution leaves undissolved particles that appear as optical defects in the cast interlayer. Compliance for the final interlayer is evaluated under ECE R43 for optical quality and adhesion performance, and the PVOH feedstock itself is registered under REACH Regulation 1907/2006.

    When Cementitious Tile Adhesives Need Open Time Without Set Retardation

    Dry-mix formulations containing 0.2–0.8 wt% Kuraray POVAL 20-98 M are used in cement-based tile adhesives, skim coats, and exterior insulation and finishing system base coats to increase water retention and improve adhesion to low-absorptive substrates. The powder is dry-blended with cement, sand graded between 0.1 and 1.0 mm, and cellulose ether in a horizontal ribbon mixer for 5–10 min. The fully hydrolyzed PVOH does not dissolve completely in cold water at 20 °C, but disperses under alkaline cement hydration and high-shear mixing; this delayed dissolution mechanism extends open time without the immediate viscosity spike associated with fully cold-water-soluble grades. Mixed mortar is applied with a 6 mm × 6 mm notched trowel and tested according to EN 1348 for tensile adhesion after 28 days of standard storage and after water immersion. Formulations are classified under EN 12004 for cementitious adhesives. The PVOH addition contributes to pot life and slip resistance, but the operational ceiling is 1.0 wt%; above this level set retardation and air entrainment increase, and compressive strength measured by EN 196-1 may fall below the required class. The grade is used together with methyl hydroxyethyl cellulose because PVOH alone does not provide sufficient water retention at low mortar thickness. The main process boundary is application below 5 °C, where dissolution of the fully hydrolyzed grade is too low to develop full binder contribution. The final cementitious products include C2TE and C2TES1 tile adhesives for porcelain tile installation, gypsum-based repair compounds, and polymer-modified cement slurries for floor leveling.

    On shuttleless weaving lines running air-jet or rapier looms, Kuraray POVAL 20-98 M is applied as a warp size for spun cotton, polyester/cotton, and viscose warps where high abrasion resistance is required at low size add-on. Size box temperature is maintained at 85–95 °C, and the size liquor is made down at 8–15 wt% solids, either as a single-component size or blended with starch or acrylic co-binder. The solids pick-up on warp yarn is controlled to 8–12 dry mass% by squeeze roller pressure and slasher speed. Dry-can temperatures are staged from 120 °C to 90 °C to prevent skinning and to maintain residual moisture at 6–8 mass% before leasing. Sized yarn tensile properties are measured by ASTM D2256, and loom efficiency is monitored on high-speed air-jet installations at insertion rates above 1000 m/min. The fully hydrolyzed structure produces a tough, crystalline size film with low cold-water solubility, so removal requires desizing at 80–95 °C in an alkaline bath containing sodium persulfate or hydrogen peroxide; PVA is not broken down by amylase alone. Residual PVOH on fabric is confirmed by iodine-boric acid color reaction before dyeing because any residual film can interfere with reactive dye diffusion and cause crack marks on sanforizing. The grade is applicable to indigo denim face yarns, filament polyester/cotton shirtings, and industrial canvas. The operational boundary is the high desizing temperature; plants without pressurized wash boxes or multi-box open-width ranges may retain PVOH residues, which appear as stiff hand after finishing. Occupational exposure and effluent controls follow the REACH Regulation 1907/2006 and the Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List; PVOH is not restricted but conventional desizing effluent must be treated for high COD before discharge.

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    Certification & Compliance
    More Introduction

    KURARAY POVAL 20-98 M is a fully hydrolyzed poly(vinyl alcohol) resin supplied as granules or powder. The product code contains three information elements: the numeral 20 defines the nominal viscosity band, the numeral 98 defines the nominal degree of hydrolysis, and the suffix M identifies the product variant within the Kuraray Poval series. On a 4% aqueous solution at 20 °C, the specified viscosity is 20.0–22.0 mPa·s. The degree of hydrolysis is 98.0–99.0 mol%, leaving a residual acetyl group content of 1.0–2.0 mol%. The high hydrolysis level increases intermolecular hydrogen bonding and crystalline order relative to 88 mol% grades, which alters solubility, film mechanics, and water resistance. The material is used in hot-water-soluble binder, sizing, and adhesive systems; film property comparisons are conventionally performed under ISO 527-3 or JIS K6726 test conditions.

    Analytical Specification Boundaries and Compliance Methods

    Table 1 lists the analytical boundaries for the grade. The test methods are drawn from JIS K6726:1994, the Japanese standard for poly(vinyl alcohol) testing; alternative reporting under ISO 15023-1:2017 and ASTM D2364-15 may be agreed with the supplier. Volatile matter and ash content are lot-release parameters because they affect solution quality and storage behavior.

    PropertySpecified boundaryTest method
    Viscosity, 4% aqueous solution, 20 °C20.0–22.0 mPa·sJIS K6726:1994
    Degree of hydrolysis98.0–99.0 mol%JIS K6726:1994
    Volatile matter≤5.0%JIS K6726:1994
    Ash content≤0.4%JIS K6726:1994
    pH, 4% aqueous solution5.0–7.0JIS K6726:1994

    On production-scale jacketed stirred vessels, solution preparation follows a dispersion-first sequence. The dry resin is added slowly to cold water under agitation before heat is applied. The dispersion is then heated to 85–95 °C and held at temperature for 30–60 minutes under moderate shear. At temperatures below 80 °C, fully hydrolyzed PVOH granules swell but do not fully disengage polymer chains, leaving microgel particles that can plug slot dies, size-press rolls, and spray nozzles. The minimum dissolution temperature is therefore a process boundary, not a quality defect. High-shear rotor-stator mixing can disperse residual gels after dissolution, but it does not remove the thermodynamic requirement for elevated temperature. For closed-loop process control, in-line viscosity measurement is recommended because the relationship between solids content and viscosity is nonlinear and varies with the thermal history of the solution.

    Why Does a Narrow Dissolution Window of 90 ± 5 °C Control Production Risk?

    Because the fully hydrolyzed chain requires thermal energy for chain disentanglement, the dissolution window for 20-98 M is operationally 90 ± 5 °C in atmospheric batch vessels. Below 85 °C, the granules swell but chain disentanglement is incomplete; the remaining microgels are visible as translucent specks and can plug size-press inlets, spinnerets, or coating filters with mesh apertures below 100 µm. Above 95 °C, water evaporation from open vessels increases surface skinning and local concentration, and prolonged exposure contributes to mild chain scission that lowers solution viscosity. The process conflict is therefore a narrow thermal window, not a broad hot-water solubility range. Production-scale jacketed vessels with indirect steam heating and high-torque anchor or helical agitators are generally operated at 90 °C for 30–60 min. High-shear rotor-stator units can polish a prepared solution after cooling to 60–70 °C, but they cannot rescue a batch that was never brought above 85 °C. Batch-to-batch variance in particle size distribution can shift dispersion time; mills using continuous dispersers should recalibrate feed rate when switching from a standard grade to the M variant. In-line viscometry at 20 °C on a recirculating sample loop is used because the 4% solution viscosity of 20.0–22.0 mPa·s is the release control point.

    When Borate Ions Are Introduced into a 20-98 M Solution

    When boric acid or borax is metered into a 20-98 M solution, didiol complexation induces reversible gelation through borate ester formation with 1,2-diol units on the PVOH chain. This response is exploited in adhesive and textile size formulations to build viscosity and tack, but the process is concentration- and pH-sensitive. At pH 8–10, borate gelation can occur within 10–60 seconds; at pH below 7, the equilibrium shifts toward the uncomplexed chain and viscosity gain is reduced. In a typical adhesive compounding batch, a 10–15 wt% PVOH solution is prepared first, cooled to 60–70 °C, and a borate solution is metered under high-shear agitation. Localized high borate concentration produces gel particles that are difficult to re-disperse. The addition rate should be limited to 0.5–2.0 parts per hundred resin borax solids on dry PVOH for controlled viscosity build; exact levels depend on required open time and wet tack. Glyoxal crosslinking is used where irreversible wet strength is required; addition of 0.5–2.0 wt% glyoxal at acidic pH followed by heat curing above 100 °C forms acetal crosslinks. Avoid simultaneous addition of borate and glyoxal in the same feed line because the reaction pathways are pH-incompatible and can cause precipitation or premature gelation.

    In paper surface sizing, 20-98 M is applied as a 2–5 wt% aqueous solution at 50–70 °C through a size press or film press. Surface strength after drying is commonly evaluated by IGT pick resistance under ISO 3783:2006; water uptake is measured as Cobb value under ISO 535:2014. Starch may be blended with the PVOH at a dry ratio of 50:50 to 70:30 PVOH:starch, but the starch fraction reduces water resistance and modifies the drying curve. In textile warp sizing, the grade is cooked to 6–12 wt% solids and applied at 60–80 °C on multi-cylinder sizing machines. The moderate viscosity allows penetration into warp yarns while depositing a film with sufficient cohesion for high-speed weaving; desizing is performed at 80–90 °C because the film is not cold-water-soluble. For ceramic green bodies, a 2–6 wt% solution is incorporated in a planetary mixer or ball mill as a temporary binder; the low ash specification of ≤0.4% is selected because inorganic residue after debinding at 350–500 °C can alter sintering densification. Users should optimize the binder content against green density and burnout schedule; published data for this specific grade in ceramic tape casting is limited.

    How Does 20-98 M Differ from Lower-Hydrolysis and Higher-Viscosity Poval Grades?

    Among the variables controlling PVOH grade selection, hydrolysis level and viscosity exert the largest influence. 20-98 M combines a high hydrolysis level with a mid-range 4% solution viscosity. Compared with partially hydrolyzed 20-88, which has a specified hydrolysis range of 86.5–89.0 mol% and a similar viscosity band, 20-98 M requires hot-water dissolution at 85–95 °C, whereas 20-88 disperses in cold water at 20–30 °C. The higher hydrolysis level increases the crystalline fraction after drying, producing films with lower elongation and greater tensile strength under ISO 527-3. Compared with 5-98, a low-viscosity fully hydrolyzed grade at 4.5–5.5 mPa·s, 20-98 M provides higher film toughness and higher adhesive strength at the same solids concentration, but its solution viscosity limits the maximum usable solids level in spray-drying and high-solids coating. Compared with 28-98 or 40-98, 20-98 M has lower molecular weight and lower solution viscosity, allowing faster pumping and higher solids at equivalent process viscosity; the trade-off is reduced film tear resistance and lower wet strength after curing. In emulsion polymerization, partially hydrolyzed grades such as 20-88 are preferred because their residual acetyl groups lower interfacial tension and promote particle nucleation. 20-98 M can be used as a co-protective colloid where higher film water resistance is required, but it is not a drop-in replacement for 88 mol% grades in cold-water-stable emulsion systems.

    Parameter20-98 M20-885-9828-98
    4% aqueous solution viscosity, 20 °C20.0–22.0 mPa·s19.0–21.0 mPa·s4.5–5.5 mPa·s27.0–29.0 mPa·s
    Degree of hydrolysis98.0–99.0 mol%86.5–89.0 mol%98.0–99.0 mol%98.0–99.0 mol%
    Dissolution temperature, atmospheric water85–95 °C20–30 °C85–95 °C85–95 °C
    Typical aqueous use concentration in sizing or adhesive2–6 wt%4–12 wt%10–20 wt%1–4 wt%

    Operational Limits Appear Most Sharply in High-Humidity Storage and Oxidative Environments

    Storage at high relative humidity changes the handling behavior of 20-98 M. The resin is hygroscopic and should be stored in tightly closed containers at 5–35 °C and relative humidity below 60%. Exposure to higher humidity can raise volatile matter above the specified ≤5.0% and cause particle agglomeration. Pre-drying at 60–80 °C for 2–4 hours may be required before use in moisture-sensitive compounding. Prolonged heating above 200 °C causes chain scission and liberation of acetic acid; processing in air at high temperature should be vented. Strong oxidizing agents, concentrated acids, and certain transition metal salts degrade PVOH and reduce solution viscosity over time. Uncontrolled addition of boric acid, borax, or glyoxal can produce irreversible gels or coagulum in feed lines; the addition sequence and pH must be controlled. Regulatory compliance under EU REACH (Regulation (EC) No 1907/2006), EU RoHS Directive 2011/65/EU, and FDA 21 CFR 175.105, 175.300, 176.170, 176.180, or 177.1670 should be verified against the specific end-use and lot certificate because grade-level regulatory status cannot be assumed for all food-contact or medical applications.