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Anhui Liwei Chemical Co., Limited.

GOHSENOL EG-40C

    • Product Name: GOHSENOL EG-40C
    • 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 702342
    Chemical Name Polyvinyl Alcohol
    Cas Number 9002-89-5
    Molecular Formula (C2H4O)n
    Appearance White granular powder
    Degree Of Hydrolysis 86.5-89.0 mol%
    Viscosity 4 Aqueous Solution At 20 C 40-46 mPa·s
    Ph 4 Aqueous Solution 5.5-7.0
    Volatile Content ≤5.0%
    Ash Content ≤0.5%
    Bulk Density 0.5-0.6 g/cm³
    Specific Gravity 1.27-1.31
    Solubility Soluble in hot water; practically insoluble in organic solvents

    As an accredited GOHSENOL EG-40C factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing GOHSENOL EG-40C is packaged in 25 kg multi-layer paper bags with PE liner, ensuring safe handling and moisture protection.
    Container Loading (20′ FCL) GOHSENOL EG-40C is loaded into a 20′ FCL container, secured on pallets, dry, ventilated, and protected from moisture.
    Shipping GOHSENOL EG-40C (polyvinyl alcohol) ships as a white granular powder in multi-layer paper/PE bags, typically 20 kg. It is non-hazardous/non-DG under normal transport conditions. Keep dry, protect from moisture, and avoid dust generation during handling. Standard truck, sea freight, or air cargo with proper labeling is suitable.
    Storage Store GOHSENOL EG-40C in a cool, dry, well-ventilated area away from direct sunlight, heat, and moisture. Keep the container tightly closed when not in use and avoid generating dust. Store in original packaging, separated from incompatible materials, and follow standard polyvinyl alcohol handling precautions.
    Shelf Life Shelf life is 2 years from manufacture date when stored unopened in original container under cool, dry conditions.
    Application of GOHSENOL EG-40C

    GOHSENOL EG-40C is a partially saponified poly(vinyl alcohol) resin with a nominal 4% aqueous solution viscosity of 40 mPa·s at 20°C and a degree of hydrolysis of 86.5–89.0 mol% when tested according to JIS K6726. The following application scenarios are restricted to manufacturing segments where partial hydrolysis and medium-viscosity solution rheology provide measurable process function: emulsion polymerization, paper surface sizing, textile warp sizing, ceramic tape casting, remoistenable adhesives, and solution-cast water-soluble film.

    What Changes in Emulsion Viscosity and Coagulum Occur When the Protective Colloid Feed Is Held Above 90°C During VAE Polymerization?

    GOHSENOL EG-40C is dissolved in demineralized water at 85–95°C under low-shear agitation until a clear solution with gel specks below 0.1 wt% is obtained, then cooled to 30–40°C before transfer to the reactor feed system. In continuous vinyl acetate-ethylene emulsion polymerization, the protective colloid solution is metered into the pre-emulsion and monomer feed at a combined rate of 3.5–7.0 wt% of total monomer feed. The reactor train comprises a high-pressure stirred CSTR with an external recirculation loop, pitched-blade or anchor impeller, and jacket cooling sized for exotherm removal at 40–60 bar ethylene partial pressure and 80–85°C polymerization temperature. At colloid dosing below 3.5 wt%, particle coalescence produces coil and heat-exchanger coagulum within 12–18 h of continuous operation. Above 7.0 wt%, final dispersion viscosity rises to 8,000–12,000 mPa·s at 25°C under ISO 2555 spindle 5 at 20 min⁻¹, causing pressure fluctuation across 80-mesh discharge filtration and unstable stripping-column feed.

    The 86.5–89.0 mol% hydrolysis window of EG-40C provides a controlled concentration of acetate groups for graft reaction with vinyl acetate radicals during polymerization. The resulting graft copolymers orient at the droplet interface and suppress irreversible coalescence without requiring anionic surfactants. Particle size distribution in finished dispersions remains between 1.0 μm and 3.5 μm when the colloid solution is cooled below 40°C prior to addition. If the solution is introduced above 40°C, localized thermal destabilization of seed particles broadens the particle size distribution and increases 400-mesh residue by a factor of 2–3 over the same reactor residence time. pH is maintained between 3.8 and 5.5; amine-based coalescent additives or ammonia neutralizers above 0.1 wt% raise pH and promote deacetylation of the colloid at reactor temperature, which reduces steric stabilization and increases wall fouling. Residual vinyl acetate is stripped in a vacuum column to below 1,000 mg/kg before final viscosity adjustment.

    Compliance for emulsion products depends on the finished adhesive or binder market. Food-contact adhesives are assessed under FDA 21 CFR 175.105; paper and paperboard components under FDA 21 CFR 176.170 and FDA 21 CFR 176.180. EU/EEA supply requires registration under REACH (EC) 1907/2006 and SVHC content below 0.1 wt%. Emulsion solids are controlled per ISO 3251, Brookfield viscosity per ISO 2555, and particle size distribution by laser diffraction per ISO 13320. Terminal dispersion products include wood assembly PVAc adhesives, paper-laminating adhesives, bookbinding adhesives, carpet-backing compounds, and construction emulsions.

    In surface sizing of uncoated fine paper and board, GOHSENOL EG-40C is introduced as an auxiliary binder in oxidized starch solutions at 5–15 dry parts per 100 parts total size solids. The metered size press or film press is operated at 6–10 wt% size solids, 60–70°C bath temperature, and 20–80 mPa·s application viscosity at 60°C. Dry pick-up is controlled at 0.3–0.8 g/m² per side. After size application, after-dryer sections run at 120–130°C surface temperature to remove water without skinning the starch-PVA film. Inline filtration through 100-μm screens is required to remove gel particles arising from humectant or salt contamination. The sizing operation improves surface strength, reduces picking during offset lithography, and narrows ink bleed variability on commercial inkjet papers.

    Finished-paper contact conditionCompliance frameworkTest method designationControlled formulation/process parameter
    Dry food contact paper/boardFDA 21 CFR 176.180FDA extraction protocolsEG-40C at 5–15 parts per 100 parts total size solids
    Aqueous and fatty food contact paperboardFDA 21 CFR 176.170FDA extraction protocolsdry add-on ≤ 0.8 g/m² per side
    EU food contact packaging materialsEC 1935/2004EN 1186 migration test seriesoverall migration ≤ 10 mg/dm²
    Cobb water absorptionISO 535:2014ISO 535:201420–35 g/m² at 60 s

    Terminal paper and board products include offset printing papers, inkjet commercial papers, folding boxboard, and release base papers. The operational boundary for high-speed converting is the solution gel point at low shear: once size viscosity exceeds 80 mPa·s at 60°C, film splitting and misting at the size press increase, and the bath must be diluted or the EG-40C portion reduced.

    Slasher Sizing of Polyester/Cotton Warp Yarns with Medium-Viscosity Partially Saponified Poly(vinyl alcohol)

    EG-40C is combined with thin-boiling starch, acrylic co-binder, and wax lubricant at 35–55 dry parts per 100 parts total size solids. Slasher trough solids are maintained at 8–12 wt%, bath temperature at 80–85°C, and application viscosity at 40–60 mPa·s at 85°C. Squeeze roll pressure is set between 20 kN/m and 40 kN/m depending on yarn count; dry add-on target is 8–11 wt% on dry warp yarn. Drying cylinder temperatures are zoned from 110°C to 135°C to prevent surface skinning and preserve film flexibility. Warp lines run at 60–100 m/min for fine-count ring-spun yarns; coarser yarns require lower speed to complete size film coalescence. Textile chemical residue compliance is assessed under OEKO-TEX Standard 100 Annex 4, and restricted substance controls follow ZDHC MRSL 3.1. The sized warp beam is conditioned at 20–23°C and 65–68% RH before loom placement because film embrittlement occurs below 12% moisture. Terminal fabrics include workwear, shirting, home textiles, and automotive seat back liners.

    Ball-milled aqueous slurries for alumina and zirconia multilayer ceramic tape casting require a pyrolytically clean temporary binder that decomposes below 600°C in air without leaving alkaline residues. GOHSENOL EG-40C is introduced at 1.5–3.5 wt% based on dry ceramic powder after the slurry has reached a particle size distribution of D50 ≤ 1.5 μm. The slurry is processed in a planetary mill or recirculating bead mill at 25–35°C for 12–24 h, followed by vacuum deairing at 50–100 Pa to remove entrained voids. Tape casting onto a silicone-coated Mylar carrier uses a doctor blade gap of 0.3–0.8 mm and carrier speed of 0.3–1.0 m/min, yielding green tape thickness between 0.05 mm and 0.15 mm after drying. Debinding follows a staged profile of 2°C/min to 250°C, 2 h hold, then 1°C/min to 500°C, 1 h hold, before sintering. Residual ash from the binder must remain below 0.1 wt% to avoid shifting sintering shrinkage; incoming EG-40C lot ash is verified per JIS K6726. Process controls are maintained under ISO 9001:2015; finished substrates for electronic applications are tested per IPC-TM-650 2.5.5.2 where dielectric properties are relevant. Terminal products include multilayer ceramic capacitors, alumina substrates, oxygen sensors, and solid oxide fuel cell electrolytes.

    When Dextrin/EG-40C Gumming Solutions Are Applied by High-Speed Roller Coater for Remoistenable Envelope and Stamp Adhesives

    Remoistenable front-sealing gum is formulated with EG-40C at 20–40 dry parts per 100 parts of low-DE dextrin, plus plasticizer and anti-blocking agent, then processed as an aqueous solution at 40–50 wt% solids. The gumming station uses a reverse-gravure or three-roll offset coater running at 150–300 m/min; dry coating weight is maintained at 5–12 g/m². Drying uses high-velocity air at 80–100°C, followed by moisture reconditioning to prevent film curling. Activation on automated mailing lines requires rewetting with water at 15–25°C under compression of 0.2–0.5 N/mm². Food-contact adhesive status is assessed under FDA 21 CFR 175.105; EU food-contact materials are evaluated under EC 1935/2004 with migration testing per EN 1186. Terminal products include envelopes, stamps, labels, and window patch gumming. At EG-40C addition above 40 parts, high-speed inserter tack increases blocking during humid storage above 60% RH; anti-blocking talc or release-coated stacking is required.

    Solution-Cast Water-Soluble Film Drying and Release Characteristics in Mold Releasing and Transfer Backing

    Solution casting of EG-40C at 15–25 wt% aqueous solids with plasticizer at 5–15 parts per 100 parts poly(vinyl alcohol), using glycerol or sorbitol, produces water-soluble transfer film without the thermoforming step used for rapid-dissolve detergent capsules. The solution is deaerated and fed through a slot die onto a chrome-plated belt or release paper; drying occurs in multi-zone air flotation dryers at 60–85°C. Film thickness is controlled between 20 μm and 60 μm, and residual moisture is conditioned to 8–12 wt% before winding. At 20 wt% solids, solution viscosity exceeds 10,000 mPa·s, requiring vacuum deaeration and positive-displacement feed. Film dissolution in cold water is governed by hydrolysis degree and plasticizer level. Terminal products include embroidery support films, water-soluble splicing tape for paper machine tail threading, temporary release sheets for prepreg layup, and mold release interleaves for composite lamination. Compliance for textile transfer backings follows OEKO-TEX Standard 100 Annex 4; biodegradability screening for water-soluble packaging components may use OECD 301B or ISO 14851. Winding and storage must be conducted below 65% RH because film tackiness increases above this threshold and interleaving or climate-controlled slitting is required.

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    Certification & Compliance
    More Introduction

    GOHSENOL EG-40C is a partially hydrolysed polyvinyl alcohol (PVOH/PVA) powder manufactured under the GOHSENOL line by Nippon Gohsei. The grade is controlled by a 4 wt% aqueous solution viscosity of 40.0–46.0 mPa·s at 20°C, hydrolysis degree of 86.5–89.0 mol%, volatile matter of ≤5.0%, ash of ≤0.5% calculated as Na₂O, and pH of 5.0–7.0 in the same solution. The analytical basis for these release limits is JIS K6726:1994. This composition leaves 11.0–13.5 mol% residual vinyl acetate units, which lower interchain hydrogen bonding and confer cold-water dispersibility while limiting dry-film water resistance relative to fully hydrolysed PVOH.

    Release specification for GOHSENOL EG-40C
    ParameterMethodLimit
    Hydrolysis degreeJIS K6726:199486.5–89.0 mol%
    Viscosity, 4 wt% aqueous solution at 20°CJIS K6726:1994 / ISO 2555:201840.0–46.0 mPa·s
    Volatile matterJIS K6726:1994≤5.0%
    Ash, as Na₂OISO 3451-1:2019 / JIS K6726:1994≤0.5%
    pH of 4 wt% solutionJIS K6726:19945.0–7.0

    What Molecular Parameters Distinguish EG-40C from Fully Hydrolysed PVOH Grades?

    Partial hydrolysis in EG-40C leaves 11.0–13.5 mol% residual vinyl acetate units distributed along the polyvinyl alcohol backbone. These acetate side groups interrupt the regular hydrogen-bonded lattice that dominates fully hydrolysed grades with hydrolysis above 98 mol%. Consequently, EG-40C dissolves more readily in cold water but produces films with greater equilibrium moisture sorption and lower tensile modulus. The medium viscosity specification of 40.0–46.0 mPa·s indicates a high molecular weight fraction that increases chain entanglement; this is advantageous for protective-colloid efficiency but raises pressure drop in transfer lines. Crystallinity differences between EG-40C and fully hydrolysed reference films can be quantified by differential scanning calorimetry according to ISO 11357-3:2018, where the partially hydrolysed grade exhibits a lower heat of fusion and a broader melting endotherm.

    Distinguishing characteristics of EG-40C versus fully hydrolysed PVOH reference grades
    ParameterEG-40CFully hydrolysed PVOH referenceStandard/method
    Hydrolysis degree86.5–89.0 mol%≥98 mol%JIS K6726:1994
    Residual acetate11.0–13.5 mol%≤2.0 mol%Calculated by difference
    Cold-water solubilityDispersible at 25–35°C; heating required for full solutionRequires heating to 70–90°CJIS K6726:1994
    Dry-film water resistanceLowerHigherFilm immersion, formulator evaluation
    Protective-colloid efficiency in vinyl acetate polymerisationHigherLowerParticle size by ISO 22412:2017
    Cast-film crystallinityLowerHigherISO 11357-3:2018

    Dissolution of EG-40C is performed in a jacketed stainless-steel vessel equipped with a draft-tube disperser or a low-shear turbine. Powder is educted into ambient demineralised water at 25–35°C under agitation of 300–600 rpm to prevent lump formation. The slurry is heated at 1–2°C/min to 85–90°C and held for 30–45 min; direct steam sparging is avoided because localised heating above 95°C produces gel specks. After cooling to 40–50°C, the solution is passed through a 100–150 µm bag filter. Solutions held longer than 48 h at ambient temperature require a preservative or chilled storage below 10°C.

    Protective-colloid performance in semi-batch vinyl acetate polymerisation is sensitive to the ratio of EG-40C to monomer and to initiator feed profile. At colloid loadings below 2 pphm, latex particle size can exceed 1.0 µm and coagulum in a baffled 4 L glass reactor equipped with an anchor stirrer at 120–180 rpm increases when the initiator pulse is introduced before the emulsion pre-charge reaches reaction temperature. At loadings above 8 pphm, latex viscosity rises sharply because excess water-soluble polymer remains in the serum, reducing heat transfer in a 4 m³ stainless-steel reactor. The processing window is therefore narrow; users should map particle size by dynamic light scattering (ISO 22412:2017) and residual monomer by gas chromatography (ISO 13741-1) across the intended colloid range. In vinyl acetate–ethylene systems, EG-40C alone may not provide sufficient interfacial area control, so a supplementary anionic surfactant at 0.1–0.5 pphm is often used. Higher anionic surfactant addition competes with the grafted PVOH layer and can increase grit formation. Persulphate initiation at 70–85°C promotes chain transfer to PVOH and anchors the colloid to the particle; redox initiation at 60–65°C leaves a larger water-soluble PVOH fraction in the serum and increases low-shear latex viscosity.

    When EG-40C Is Substituted for Fully Hydrolysed PVOH in Water-Resistant Adhesive Compounding

    Substitution of fully hydrolysed PVOH with EG-40C in adhesive compounding reduces solution make-up temperature but also reduces the equilibrium wet strength of the dried adhesive film. In paper tube winding and remoistenable labelling, the partially acetylated grade contributes faster tack development and lower crystallisation-induced shrinkage on porous substrates. Unmodified films derived from EG-40C absorb water and lose cohesive strength, so wet-service formulations require addition of a crosslinker such as glyoxal, a polyisocyanate, or zirconium ammonium carbonate. Bond strength is evaluated by lap-shear adhesion testing on paper-based adherends under TAPPI T 494 or ISO 1924-2:2008, with specimens conditioned to equilibrium at 23°C and 50% RH as defined in ISO 187. In a production laminating line with a slot-die applicator, insufficient drying below 80°C leaves residual moisture at the bond line and produces delamination under reel tension.

    At the size press, EG-40C is applied as a 3–6 wt% solution at 40–60°C using a metering size press or film press. The grade functions as a film-forming binder that reduces surface dusting and improves IGT pick resistance of uncoated fine paper; performance is evaluated by ISO 3783:2006 using a medium-viscosity oil at specified printing speed. Because the 4 wt% solution viscosity is already 40.0–46.0 mPa·s, recirculation loops require positive displacement or progressive cavity pumps; centrifugal pump selection at line sizes below 50 mm risks cavitation and uneven flow distribution across the press width. At 3 wt% application solids, a rod-metering size press deposits 0.3–0.8 g/m² dry binder depending on rod pressure and base sheet absorption. If the base sheet is internally sized with alkyl ketene dimer above 0.15% oven-dry pulp, solution holdout increases but the failure mode may shift from fibre tear to interfacial binder detachment.

    Rheological Limits, Borate Sensitivity, and Biological Stability

    EG-40C solutions are pseudoplastic at industrial concentration; apparent viscosity declines with increasing shear rate in blade and roll applicators. The colloid is incompatible with borate salts and boric acid, which crosslink with the 1,3-diol segments of PVOH and produce gelation or precipitate in the mixing head. Recycled process water from papermaking should be monitored for residual borate or hardness ions because gel aggregates above 0.1 mm can block slot-die lips and cause coating streaks. Storage of unstabilised solutions at ambient temperature beyond 48 h risks microbial growth; a preservative compatible with nonionic polymers is required, or the solution should be held at 60–70°C under low agitation. Viscosity loss during storage may also indicate oxidative main-chain scission if the solution is exposed to copper or iron ions; stainless steel or plastic wetted parts are specified.

    Regulatory Status Is Governed by Specific Monograph Conditions

    Use of EG-40C in food-contact adhesives and paper coatings requires formulation-specific verification against regional positive lists. Polyvinyl alcohol grades may be used in adhesives intended for food packaging under FDA 21 CFR §175.105 and as a component of paper and paperboard under FDA 21 CFR §176.170 and §176.180, subject to extraction limitations and good manufacturing practice. In the European Union, compliance with Commission Regulation (EU) No 10/2011 must be verified for the final article by migration testing according to EN 1186-1:2002 and EN 1186-3:2002. The grade is supplied with a REACH-compliant safety data sheet; users must confirm registration for the relevant tonnage band and ensure no national restriction applies.

    Why Does Fines Generation Compromise Continuous Emulsification Feed Accuracy?

    Pneumatic transfer of EG-40C powder through dilute-phase conveying systems generates fines when line velocity exceeds 20–25 m/s and when elbow radius is below 5D. Fines accumulation in receiving vessels alters bulk density and can shift gravimetric feeder output by ±3–5% in continuous emulsification. A closed-loop nitrogen conveying system with dew point below -40°C reduces hygroscopic clumping. Bulk bags should be stored at ≤30°C and ≤60% RH; opened bags should be resealed because exposure to humidity above 60% RH can increase moisture content and reduce dissolution consistency. If the powder is pre-blended with starch in dry adhesive mixes, the difference in bulk density between EG-40C and native starch requires separate venturi pick-up points to avoid segregation in the feed hopper.

    EG-40C is also used as a temporary binder in ceramic green tape and as a suspension stabiliser in water-based pigment dispersions. In ceramic tape casting, a 8–12 wt% solution is blended with inorganic powder and plasticiser; the dried tape must exhibit no surface skinning, which is suppressed by humidifying the drying air to 50–60% RH. Because the grade is partially hydrolysed, it burns out at lower ash residue than fully hydrolysed PVOH if the ash specification is maintained; this is relevant for electronic ceramic formulations where sodium content must not exceed 0.5% as Na₂O. Published data for EG-40C-specific burnout behaviour in multilayer ceramic processing is limited, so formulators should validate residue by thermogravimetric analysis in air according to ISO 11358-1:2022.