| HS Code | 574421 |
| Product Name | SELVOL Polyvinyl Alcohol 09-425 Solution |
| Appearance | Clear, viscous liquid |
| Color | Colorless to pale yellow |
| Odor | Mild characteristic odor |
| Cas Number | 9002-89-5 |
| Solids Content | 9% |
| Viscosity | 425 cP at 25°C |
| Ph | 5.0 to 7.0 |
| Specific Gravity | 1.02 to 1.04 at 25°C |
| Boiling Point | Approximately 100°C |
| Freezing Point | Approximately 0°C |
| Flash Point | Non-flammable aqueous solution |
| Water Solubility | Fully miscible in water |
| Shelf Life | 12 months from date of manufacture |
As an accredited SELVOL Polyvinyl Alcohol 09-425 Solution factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in 55-gallon drums, SELVOL Polyvinyl Alcohol 09-425 Solution is a clear aqueous polymer solution for adhesives and coatings. |
| Container Loading (20′ FCL) | Load 20′ FCL with SELVOL Polyvinyl Alcohol 09-425 Solution in sealed drums or IBCs, using secure dunnage, spill containment, and proper labeling. |
| Shipping | SELVOL Polyvinyl Alcohol 09-425 Solution ships as a non-hazardous aqueous solution in sealed containers, protected from extreme heat and freezing. Use leak-proof drums or totes with proper labeling. Ensure upright positioning during transit to prevent spills. Standard ground freight is acceptable; no special hazmat endorsement required. |
| Storage | Store SELVOL Polyvinyl Alcohol 09-425 Solution in tightly sealed, labeled containers in a cool, dry, well-ventilated area. Keep away from heat, open flames, and strong oxidizers. Prevent freezing and direct sunlight, as temperature extremes can alter solution properties. Avoid evaporation and contamination by ensuring lids are securely closed when not in use. Use appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life is typically 12 months when stored sealed in original containers, protected from freezing and excessive heat. |
In fine-paper surface sizing on film-press and metering-rod machines, SELVOL Polyvinyl Alcohol 09-425 Solution is introduced into oxidized starch size-press formulations only after the cooked starch has been cooled below 70°C to avoid acid hydrolysis of the PVOH chain. The addition is set between 0.5 and 3.0 dry parts PVOH per 100 dry parts of cooked starch, corresponding to 5–30 wt% as-supplied solution in the working bath at a typical pickup of 0.8–2.5 g/m² per side. Application viscosity is held at 20–80 mPa·s at 60°C to prevent rod skipping on film-press equipment running at 60–150 m/min; production records from linerboard machines indicate that addition below 0.5 dry parts produces negligible Cobb60 improvement according to ISO 535, while addition above 3.0 dry parts increases surface film crack formation at 25–30% relative humidity. End uses include inkjet paper, folding carton stock, label facestock, and surface-sized linerboard. Compliance references include 21 CFR 176.170 for aqueous and fatty food contact paperboard, TAPPI T 441 for water absorption, and ISO 8791-4 for Parker Print-Surf roughness.
Remoistenable adhesive lines running kraft gummed tape and bottle-label compounds typically meter SELVOL Polyvinyl Alcohol 09-425 Solution into a starch or dextrin cook after the cook temperature has dropped to 55–65°C; the addition is 3–15 wt% as-supplied solution of the final wet compound, equivalent to 0.3–1.4 dry wt% PVOH. The batch is mixed under low-shear agitation at 25–80 rpm with a swept-surface planetary mixer, and viscosity is checked on a Brookfield RVT spindle at 20 rpm and 25°C against a target band of 2,000–12,000 mPa·s. A common production failure is pH drift into the range below 4.0 in high-acid dextrin systems, where anionic dextrin fragments form polyelectrolyte complexes with PVOH and produce insoluble grit; buffering with sodium phosphate to 5.5–7.0 before PVOH addition prevents the precipitation. End products include remoistenable gummed packaging tape, glass bottle label adhesives, wallpaper paste, and carbonless paper padding compounds. Compliance references include 21 CFR 175.105(a) for indirect food-contact adhesives, ASTM D1876 for T-peel adhesion, and REACH polymer information under EC 1907/2006.
During free-radical emulsion polymerization of vinyl acetate/ethylene and polyvinyl acetate homopolymers, SELVOL Polyvinyl Alcohol 09-425 Solution is fed as the primary protective colloid into the initial reactor charge and the delayed monomer feed. The charge is 2–5 dry parts PVOH per 100 parts monomer, and the as-supplied solution is diluted with deionized water after gravimetric solids check before being metered at 15–40 parts per 100 parts monomer depending on solution solids. A jacketed stainless-steel reactor with an anchor impeller operating at 80–120 rpm is used; initiation with a persulfate–sodium metabisulfite redox couple occurs between 60–80°C, and monomer is delayed over 3–5 h. The PVOH chains undergo grafting with vinyl acetate to form a steric layer that stabilizes particles in the 600–1,500 nm range; final emulsions typically show nonvolatile solids of 50–60 wt% and Brookfield viscosity between 3,000 and 12,000 mPa·s. Batch-to-batch viscosity drift above 1,000 mPa·s has been observed when returned tote storage allowed water evaporation and PVOH feed solids varied by ±0.5%; inline solids monitoring and dilution reduce this drift. The emulsions are converted into interior wall paints, wood adhesives, paperboard laminating adhesives, and carpet-backing compounds. Compliance references include 21 CFR 175.105(a) for adhesive components, 21 CFR 175.300 for resinous and polymeric coatings, and polymer exemption inventory under EC 1907/2006.
| Application sector | Regulatory/standard reference | Test method or threshold |
|---|---|---|
| Paper surface sizing | 21 CFR 176.170, ISO 535 | Cobb60 water absorption; food-contact paperboard |
| Remoistenable adhesives | 21 CFR 175.105(a), ASTM D1876 | Indirect food contact; T-peel adhesion |
| Emulsion polymerization | 21 CFR 175.300, EC 1907/2006 | Resinous and polymeric coatings; REACH polymer exemption |
| Textile sizing/nonwovens | ZDHC MRSL 3.1, ISO 14184-1 | Chemical screening; formaldehyde ≤ 16 mg/kg for infant textiles |
| Technical ceramics | ISO 18754, ASTM C373, RoHS 2011/65/EU | Density; water absorption; electronics-grade ceramic substrates |
| Building materials | EN 12004:2007+A1:2012, ASTM C474-15 | C2 tile adhesive classification; paper-to-gypsum bonding |
Thermal profiles on slasher frames and air-laid nonwoven lines differ substantially, because SELVOL Polyvinyl Alcohol 09-425 Solution must remain water-soluble on warp yarn for desizing but must form a cured binder film in nonwoven webs. For spun cotton and cotton/polyester warp sizing, the product is combined with native starch at 2–8 dry wt% of starch solids, applied in a slasher at squeeze roller pressures of 2–4 bar, and dried on cylinders at 90–120°C; downstream desizing uses 0.5–1.0 wt% sodium hydroxide at 85°C, which raises effluent COD. For air-laid and wet-laid nonwoven binder, the solution is sprayed or padded at 4–10 wt% as-supplied solution of web weight and cured at 130–150°C in through-air ovens. End products include woven apparel fabrics, bed sheeting, scrim-reinforced nonwovens, and air-laid wipes. Compliance references include ZDHC MRSL 3.1, ISO 14184-1 for formaldehyde limit of 16 mg/kg in infant textiles, and OEKO-TEX Standard 100 as a voluntary finished-article scheme.
Technical ceramic powder processing with SELVOL Polyvinyl Alcohol 09-425 Solution uses the product as a green-body binder in alumina, zirconia, and silicon nitride slip systems. The addition is 0.3–2.0 dry wt% of ceramic powder, usually applied as 2–8 wt% as-supplied solution of the aqueous slip weight before bead milling to a median particle size below 0.8 µm. The slip is adjusted to pH 9.0–10.0 with ammonia and spray-dried at inlet 180–220°C and outlet 90–110°C; green density measured by Archimedes is maintained at 2.35–2.50 g/cm³ for dry-pressed alumina. A cliff-edge is documented above 2.5 dry wt% PVOH: increased binder volume after ejection produces lamination cracks, and debinding at 350–500°C in air for 2–6 h leaves interconnected porosity channels if the burnout plateau is shortened. Residual ash for electronic-grade substrates is held below 0.1 wt%. End products include alumina substrates, spark plug insulator bodies, ceramic tile granulate, and silicon nitride bearing preforms. Compliance references include ISO 18754 for fine-ceramic density, ASTM C373 for water absorption, and RoHS 2011/65/EU where electronic ceramic substrates enter electrical equipment.
In dry-mix gypsum joint compounds and cementitious tile adhesives, SELVOL Polyvinyl Alcohol 09-425 Solution is introduced either as a liquid component in ready-mix compounds or pre-blended with cellulose ethers in dry-mix formulations. The dosage is 0.1–0.8 dry wt% of total dry mix, equivalent to 0.5–3.0 wt% as-supplied solution in liquid compounds. Ready-mix joint compounds are mixed with a helical blade at 500–1,000 rpm after cellulose ether hydration, and the paste is tested for open time according to EN 1346 and tensile adhesion according to EN 1348 for C2 cementitious tile adhesives. Water retention is measured by ASTM C474 for paper-to-gypsum bonding. Above 0.8 dry wt% PVOH, open time can be extended, but compressive strength may decline because PVOH films around cement grains inhibit late-age hydration; mixing with borate-crosslinked starch in alkaline cement systems can also produce over-thickening. End products include ready-mix joint compound, C2 tile adhesive, gypsum skim coat, and self-leveling underlayment. Compliance references include EN 12004:2007+A1:2012, ASTM C474-15, and REACH.
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SELVOL Polyvinyl Alcohol 09-425 Solution is supplied as a ready-to-use aqueous polyvinyl alcohol solution for industrial formulation and coating operations. The 09-425 designation is a manufacturer-specific product code; publicly available specification values for this exact solution are limited, so the lot certificate of analysis is the controlling document for solids content, viscosity, pH, degree of hydrolysis, ash, and preservative content. The solution form removes dry-powder handling steps such as dust extraction, cook-tank heating, and coarse filtration that accompany granular or powder PVOH grades. The solvent water is an active formulation constituent, not an inert diluent, and must be included in the materials balance when the solution replaces solid polyvinyl alcohol.
Because the product is pre-dissolved, incoming quality control is based on rotational viscosity and solids rather than particle size and dissolution time. A sample is conditioned in a closed container at the temperature specified by the supplier before viscosity is determined by ISO 2555 or ASTM D2196-20. Solids are determined by forced-air oven drying under ISO 3251. The pH is recorded by potentiometric method. These values are trended against the qualified baseline, and dilution water is adjusted only after solids content has been calculated.
Viscosity of aqueous polyvinyl alcohol solutions is strongly temperature-dependent. A cooled sample reports a higher rotational viscosity than a sample equilibrated at 20 °C or 25 °C, even if the polymer solids are identical. Incoming inspection therefore requires a validated temperature bath or water jacket; a variation of ±1 °C at the measurement point can create false accept/reject decisions when high-solids PVOH solutions are tested. Dilution with deionized water reduces viscosity, but water addition is made slowly under low-shear agitation to avoid local polymer precipitation. The target process viscosity is not a fixed property of the grade; it is a plant-specific set point determined by the coating or metering equipment.
For gravure, reverse-roll, and slot-die coating, viscosity is adjusted to a narrow range before use. If only viscosity is measured after dilution and solids are not rechecked, the dry coat weight may drift below the barrier specification. The diluted solution is checked for solids by ISO 3251 and for viscosity by ISO 2555; the ratio of the two values is used as a lot-control variable. Temperature correction charts for PVOH solutions are available in polymer processing literature, but the specific curve for 09-425 is generated from multiple measurements on each incoming lot.
Metering systems for aqueous PVOH use positive-displacement pumps with stainless steel wetted parts. High-speed centrifugal pumps can induce shear heating and air entrainment, which reduces film quality. Return lines from the coater discharge below the liquid surface in the feed tank to prevent foam. If the solution is left in a die or transfer line during a production stop, water evaporation forms a surface skin that can break loose as lumps. A start-up flush with warm water is used before coating is resumed. Published data for the exact 09-425 solution is limited; these handling controls are standard for high-solids PVOH solutions.
When 09-425 Solution replaces dry SELVOL powder in a water-based adhesive, the formulation water balance changes. The solution contributes water at a fixed ratio, so a direct equal-mass substitution without solids correction reduces the concentration of the co-binder and alters open time. The conversion is calculated by dividing the required dry polymer mass by the fractional solids shown on the certificate of analysis. The water contributed by the solution is then subtracted from the batch water addition. If the original formula contains pH buffers or salts, pH is checked after the full water load is present because the pre-dissolved solution can dilute the buffer before the remaining water is added.
Shear history also changes when powder is eliminated. Dry PVOH requires hydration under elevated temperature and high-shear mixing; the liquid solution requires only gentle homogenization before use. This difference improves batch-to-batch reproducibility but increases sensitivity to storage and handling. The solution is more susceptible to microbial growth than dry powder, and the preservation system is part of the product technology. If the material is stored beyond the supplier’s stated shelf life, bioburden is checked by a validated microbiological method before the solution is released for production.
In ceramic green-tape formulations, the solution is blended with ceramic powder, dispersant, and plasticizer to form a castable slurry. Water evaporation during tape drying leaves a polymer film between ceramic particles, and green strength is determined by polymer molecular weight, degree of hydrolysis, and plasticizer loading rather than by viscosity alone. A higher solution viscosity does not necessarily indicate higher binder strength; it may reflect a lower temperature, a higher solids content, or a higher molecular weight. The degree of hydrolysis from the certificate of analysis is compared with the qualified range before a new lot is accepted. Because published data for 09-425 in ceramic applications is limited, this comparison is established from plant trials under fixed casting speed and drying conditions.
In textile warp sizing, the solution is metered into size boxes for spun and filament yarns. The polymer film protects yarn from abrasion during weaving and is removed later by water washing. Formulators often blend PVOH with starch, wax, or acrylate binders; the PVOH solution is added after starch gelatinization to prevent competition for water during the starch cook. Desizing efficiency depends on the water solubility of the polymer, which is a function of the degree of hydrolysis and the heat history of the dried size film. If the size box is held above the polymer gelation temperature, film quality is maintained; if the solution cools below that temperature, surface gel can form and deposit on squeeze rolls.
For paper and board surface sizing, the solution is introduced into the size press or film press alongside starch and other additives. The ready-to-use form removes dissolution variability and reduces the burden on starch cook equipment, but the as-received solids level is included in the size press solids target. Viscosity at the press is affected by temperature and starch conversion; the PVOH fraction is adjusted by metering the liquid on a dry-solids basis. Drying after the size press is constrained by the water added with the solution. Higher wet pick-up requires additional after-dryer capacity, and papermakers monitor sheet moisture at the reel rather than assuming that the pre-dried coating will reach target moisture without dryer changes.
For barrier coatings, dried PVOH films provide oil and grease resistance and can form part of a multi-layer structure. The film must be continuous and free of pinholes. Pinholes are worsened by air entrainment, contaminated substrate, or irregular drying. Film quality is evaluated by conditioning at 23 °C and 50 % RH under ISO 291 or ASTM D618, then measuring tensile properties by ASTM D882-18 or ISO 527-3. The values are useful for lot qualification only when film preparation and drying history are fixed, because PVOH crystallinity and water content affect mechanical properties.
Aqueous PVOH solutions are pseudoplastic; the rotational viscosity measured at low shear may be higher than the apparent viscosity under coating shear. For slot-die and gravure applications, a capillary or cone-plate measurement is therefore more representative than a single-point Brookfield value. The shear rate in a slot-die feed line may differ by orders of magnitude from the rotational method, and this difference must be accounted for when setting pump speeds. Published data for 09-425 is limited, so rheological characterization is lot-specific.
The primary distinction is physical form: 09-425 is supplied as a solution, whereas adjacent SELVOL designations may be supplied as granular solid, powder, or tablet. The solution eliminates cook time and dust extraction but adds water weight and freeze sensitivity. It also has a finite shelf life, while dry grades are stable if kept dry. The grade code does not necessarily permit direct substitution with another Selvol solution of different viscosity class. A lower-viscosity solution may coat at a given solids level but produce a weaker film if molecular weight is lower; a higher-viscosity solution may require more dilution and increase drying load.
Differences between suppliers are not based on solids content alone. Additives such as preservatives, surface tension modifiers, or defoamers vary by product. The residual acetyl content affects cold-water solubility, surface activity, and film water sensitivity. A partially hydrolyzed grade generally has lower aqueous solution viscosity at equal molecular weight than a fully hydrolyzed grade, but the exact value for 09-425 is controlled by the supplier. Published data for this exact configuration is limited, so a side-by-side trial is used when substituting another PVOH solution.
Regulatory status is grade-specific. In the United States, PVOH may be used as a component of paper and paperboard under 21 CFR 176.170 or 21 CFR 176.180, or as an adhesive component under 21 CFR 175.105, depending on the end use. Direct food contact is not automatically approved for all PVOH solutions. SELVOL Polyvinyl Alcohol 09-425 Solution is covered by the supplier’s regulatory statement and the safety data sheet; lot-specific documentation is retained for audit. In the European Union, REACH registration status and food-contact requirements are verified through supplier documentation. RoHS obligations are typically not triggered for the liquid polymer itself, but the finished article may require conformity assessment under the applicable directive.
| Property | Reference method | Reporting unit |
|---|---|---|
| Rotational viscosity | ISO 2555 / ASTM D2196-20 | mPa·s |
| Solids content | ISO 3251 | % by mass |
| Degree of hydrolysis | ISO 15023-2 | mol% |
| pH | Potentiometric method | pH units |
| Film tensile properties | ISO 527-3 / ASTM D882-18 | MPa and % |
Industrial hygiene is governed by the supplied SDS. The aqueous solution is not typically classified as flammable; however, dried PVOH film is combustible organic matter. Oven exhaust ducts and dryer hoods are kept free of polymer accumulation. Ventilation is required during drying because water vapor and trace volatile by-products are released. Spills of the liquid are slippery; containment with absorbent material is used before water washing to avoid draining a high organic load into process water without authorization.
On a continuous web coating line running a PVOH/starch size, viscosity drift above the agreed control window changes the wet film thickness supplied by a blade or rod coater. If rod pressure is not adjusted, coat weight increases or decreases. Batch-to-batch variation in solution solids is normalized by changing the dilution water, not by changing rod pressure. Operators record viscosity after dilution at the same temperature, using the same spindle and speed; this prevents false adjustments based on ambient plant temperature swings.
When the machine stops, the solution can dry on rolls and applicator surfaces. The film is water-soluble and can be removed with warm water if the stop is short. If the material remains on a heated roll for extended periods, crystallization and skinning are more difficult to remove. A wetting mist or roll-washing system is configured on some coaters to keep surfaces wet during short stops. Published data for 09-425 in this specific equipment configuration is limited.
In textile sizing, ceramic tape casting, and adhesive coating, acceptance of 09-425 Solution is determined by whether the supplied water content and preservation system can be absorbed into the formulation. Drying capacity, open time, pH stability, and film clarity are plant-specific variables. A trial run with a fresh lot is performed at the normal line speed and with the standard drying profile; the resulting film or coated substrate is held for post-cure testing before the lot is released. This sequence is repeated for each new lot when the supplier’s certificate of analysis shows any change in degree of hydrolysis, solids, or viscosity beyond the agreed range.