| HS Code | 358758 |
| Chemical Name | Poly(vinyl alcohol) |
| Cas Number | 9002-89-5 |
| Appearance | White powder |
| Average Degree Of Polymerization | 2600 |
| Degree Of Hydrolysis | 88 mol% (86.0-90.0 mol%) |
| Viscosity 4 Aqueous Solution At 20 C | 60 mPa·s (55-65 mPa·s) |
| Molecular Weight | Approximately 120,000 |
| Ph 4 Aqueous Solution | 5.0-7.0 |
| Ash Content | ≤0.3% |
| Volatile Content | ≤5.0% |
| Bulk Density | 0.40-0.60 g/cm³ |
| Solubility | Soluble in hot water; insoluble in cold water and most organic solvents |
As an accredited Shuangxin 26-88 PVA (PVA 088-60) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Shuangxin 26-88 PVA (PVA 088-60) is packaged in 25 kg multi-layer kraft paper bags with an inner plastic lining for moisture protection. |
| Container Loading (20′ FCL) | Load 20′ FCL with palletized Shuangxin 26-88 PVA bags; secure, dry, ventilated container to prevent moisture damage. |
| Shipping | Shuangxin 26-88 PVA (PVA 088-60) ships as non-hazardous white powder in 25 kg airtight polyethylene-lined woven bags, palletized and containerized. Keep sealed and dry to prevent moisture absorption. Avoid dust accumulation during handling. Standard shipping documentation and certificate of analysis provided. |
| Storage | Store in a cool, dry, well-ventilated area, away from heat, open flames, and direct sunlight. Keep the container tightly sealed to prevent moisture absorption and contamination. Avoid creating dust clouds; keep away from incompatible materials. Maintain stable room temperature and dry conditions to preserve quality and extend shelf life. |
| Shelf Life | Shelf life: 24 months from manufacture when stored in a cool, dry place, away from moisture and heat. |
In suspension polyvinyl chloride (S-PVC) reactor practice, Shuangxin 26-88 PVA (PVA 088-60) is employed as a primary suspending agent rather than as a viscosity modifier. The grade is characterized by a 4% aqueous solution viscosity of 58–66 mPa·s at 20 °C in accordance with GB/T 12010.3-2010 and an alcoholysis degree of 86.5–89.0 mol% under GB/T 12010.5-2010. In a 30 m³ autoclave equipped with a turbine impeller and reflux condenser, the polymer is pre-dissolved as a 1.0–3.0 wt% aqueous solution at 80–85 °C. The polymerization charge typically maintains a water-to-vinyl chloride monomer mass ratio of 1.10:1 to 1.40:1, with the PVA dosage set at 0.04–0.08 parts per 100 parts VCM. A secondary dispersant of lower hydrolysis grade near 72.5 mol% is added at 0.01–0.03 phr to regulate droplet coalescence. Initiation is carried out with di(2-ethylhexyl) peroxydicarbonate at 0.04–0.08 phr at a reaction temperature of 55–65 °C, corresponding to an autoclave pressure of 0.85–1.05 MPa. Agitation power input is maintained at 1.0–1.5 kW/m³ because the balance between droplet breakup and coalescence determines S-PVC grain morphology. Under these conditions the resulting resin typically exhibits a K-value of 65–70, bulk density of 0.50–0.55 g/cm³, median particle size of 120–180 µm, and cold plasticizer absorption of 22–28 g DOP/100 g resin. Operational boundaries are narrow: at primary PVA additions above 0.10 phr, the particle-size distribution shifts coarse beyond 200 µm, reducing plastisol absorption and increasing the incidence of fish-eye defects in calendered sheet; below 0.03 phr, suspension stability declines and excessive fines below 40 µm are generated, increasing centrifuge separation load. Resin properties are evaluated against ASTM D1755-15 classification, ISO 4612:2018, and GB/T 5761; particle-size distribution is confirmed by laser diffraction per ISO 13320:2020.
| PVA 088-60 primary addition (phr VCM) | Median particle size D50 (µm) | Bulk density (g/cm³) | Cold plasticizer absorption (g DOP/100 g) | Observed limitation |
|---|---|---|---|---|
| 0.02 | 40–80 | 0.38–0.45 | 15–19 | High fines, poor slurry drainage |
| 0.05 | 120–180 | 0.50–0.55 | 22–28 | Balanced for general-purpose S-PVC |
| 0.08 | 170–200 | 0.53–0.58 | 24–30 | Low fines, slower degassing |
| 0.12 | >200 | 0.55–0.60 | 18–22 | Fish-eye defects, plastisol viscosity drop |
In high-viscosity vinyl acetate–ethylene (VAE) dispersion production, the 088-60 grade is not simply a thickener; it functions as a grafting substrate and colloidal stabilizer. The polymer is dissolved into demineralized water at 90–95 °C to a concentration of 10.0–15.0 wt% before being charged to a pressure reactor. Total PVA addition is controlled between 2.5 wt% and 6.0 wt% on total monomer, because the 86.5–89.0 mol% hydrolysis window is high enough to retain aqueous solubility after cooling but low enough to promote interfacial activity. During polymerization at 70–85 °C and ethylene pressure of 3.0–7.0 MPa, potassium persulfate and sodium metabisulfite are fed at a combined redox initiator loading of 0.25–0.50 wt%. Vinyl acetate radicals abstract protons from the PVA backbone, producing graft copolymers that anchor to the dispersed phase. The high degree of polymerization of 2600 in the 088-60 grade yields longer graft chains than lower-viscosity PVA, raising the aqueous-phase viscosity and improving wet-state cohesion. Emulsions with 55% solids content typically develop Brookfield RVT viscosity of 3000–12000 mPa·s at 20 rpm and 25 °C. Below a PVA dosage of 2.0 wt%, coagulum increases above 500 mg/kg and the latex exhibits shelf instability within 30 days; above 6.5 wt%, end-of-reactor viscosity can exceed 15000 mPa·s, causing transfer pump cavitation and wall fouling. The stabilized dispersions are used in wood-assembly adhesives formulated to EN 204 D2/D3 durability classes, nonwoven binder applications requiring ISO 527-3 film tensile elongation, and low-VOC interior primers. Residual vinyl acetate monomer is stripped to below 0.1 wt% before discharge, with monomer content verified by ISO 4625:2018 or an equivalent gas chromatographic technique.
| PVA 088-60 dosage (wt% on total monomer) | Final dispersion viscosity at 25 °C (mPa·s) | Coagulum after 200 mesh filtration (mg/kg) | Freeze-thaw cycles at −10 °C | Production observation |
|---|---|---|---|---|
| 2.0 | 2500–3500 | 400–800 | 1–2 | Marginal stability, fines settle after 30 days |
| 4.0 | 5000–8000 | 80–150 | 3–4 | Balanced wood-adhesive viscosity profile |
| 6.0 | 10000–14000 | 30–80 | 4–5 | High-viscosity nonwoven binder; pump dilution required |
| 7.0 | 15000–18000 | 20–60 | 4–5 | Reactor wall fouling and transfer pump cavitation observed |
In cotton/polyester warp sizing, a stock solution of the 088-60 grade is cooked at 85–95 °C for 45–60 min under high-shear mixing before being blended with oxidized starch and acrylic copolymer. The dry size recipe typically contains 20–35 parts PVA 088-60, 50–65 parts oxidized starch, 10–20 parts acrylic size, and 0.5–1.5 parts wax lubricant per 100 parts total dry solids. Final size-box solids are set between 8.0 wt% and 13.0 wt% depending on yarn count and loom speed; for 65/35 polyester/cotton 45s yarns the add-on is controlled at 8–12%, while high-density 80s yarns require 10–14%. The size-box temperature is maintained at 85–90 °C to keep the high-molecular-weight PVA in solution; below 80 °C, skinning and gel particles form on the squeeze rolls and transfer to the warp sheet. Size liquor viscosity in the box is 200–500 mPa·s at 90 °C measured by Brookfield LV spindle 2 at 30 rpm, or 18–30 s by Zahn cup #2. Drying on a multi-cylinder slasher uses Teflon-coated cylinders at 115–135 °C; final sized yarn moisture is kept at 2.0–3.5% to avoid embrittlement and static breakage. Weaving on air-jet looms at 650–850 rpm is supported by the film elasticity and reduced hairiness contributed by the high-DP PVA. Desizing after weaving is performed with amylase or oxidative desizing agents; PVA in the effluent can be recovered by ultrafiltration at 85–95% recovery efficiency. Sized yarn tensile strength is evaluated by ASTM D2256/D2256M-21, and the size formulation is screened under OEKO-TEX Standard 100 Annex 6 limits for textile auxiliaries. The formulation is unsuitable for low-humidity weaving rooms below 35% RH unless antistatic additives are introduced, because the film becomes excessively brittle at low moisture content.
In surface sizing and pigmented coating, the 088-60 grade is introduced as a cooked stock solution rather than as dry powder. For size-press application on uncoated fine paper and linerboard, the stock solution is prepared at 8.0–12.0 wt% and then injected into an oxidized starch stream so that PVA represents 10–20 parts per 100 parts dry starch solids. The working size-press liquor is held at 65–75 °C with total solids of 4.0–8.0% and viscosity of 50–120 mPa·s at 70 °C. The PVA film increases IGT pick resistance by reinforcing the starch brittle film; pick velocity is tested according to ISO 3783:2006, while Gurley air resistance is reported under TAPPI T 460. In pigment coating colors, PVA 088-60 is used at 0.5–1.5 parts per 100 parts pigment as a co-binder alongside carboxylated styrene-butadiene latex at 6.0–10.0 parts. The high aqueous-phase viscosity of this grade restricts practical coating solids to 58–62%; above 62%, blade coater pressure fluctuations and surface scratches increase because the high-molecular-weight PVA reduces low-shear mobility without improving high-shear rheology. Jet cookers are operated at 95–100 °C for 20–30 min to fully open the polymer chains, and the cooked solution is screened through 100 µm filters before addition. End products include coated folding boxboard and inkjet base paper where the PVA improves water retention and binder migration control. For pharmaceutical or food-contact paper, compliance must be confirmed against FDA 21 CFR 176.170 or BfR Recommendation XXXVI; the PVA grade alone does not confer regulatory approval unless the entire coating formulation meets applicable extraction limits.
Paper-tube and lamination adhesive batches formulated with the 088-60 grade commonly use a 10.0–14.0 wt% stock solution as the main film-forming component. A typical formulation contains 100 parts dry PVA 088-60, glycerol plasticizer at 5.0–10.0 phr, sorbitol humectant at 0–5.0 phr, mineral-oil defoamer at 0.1–0.3 phr, and benzisothiazolinone-based biocide at 0.05–0.2 phr. Dissolution is carried out in a jacketed anchor-agitated tank at 85–90 °C for 60–90 min; after cooling to 25 °C, the adhesive develops a Brookfield RVT viscosity of 12000–25000 mPa·s at 20 rpm with spindle 6. Application to spiral paper tubes is performed by roller coater at a wet coating weight of 80–150 g/m²; open time on absorbent substrates is 5–15 s. Water resistance is introduced by adding glyoxal at 0.5–1.2 phr or a blocked polyisocyanate dispersion at 1.0–3.0 phr; the working pot life then shortens to 4–8 h depending on pH and temperature. The high degree of polymerization of the 088-60 grade provides high initial tack and crush resistance, but it also raises the lower application temperature limit: below 10 °C, the adhesive exhibits thixotropic gel structure and roller transfer becomes uneven. For food-carton side-seam adhesives, the formulation may be designed to comply with FDA 21 CFR 175.105; compliance requires control of all components, not merely the PVA base. Bond performance is measured by ASTM D1876-08 T-peel and ASTM D903-98 for peel or shear; tensile shear on paper board is checked by ISO 1924-3:2005 where applicable to the substrate.
For cordierite honeycomb extrusion, the 088-60 grade is prepared as an 8.0–12.0 wt% aqueous pre-gel and added to the ceramic batch at 2.0–5.0 parts per 100 parts dry inorganic powder. A representative cordierite precursor mixture contains talc 40 parts, kaolin 25 parts, alumina 30 parts, and fused silica 5 parts, combined with deionized water at 15–18 parts, PVA 088-60 at 3.0–4.0 parts, poly(ethylene glycol) 400 plasticizer at 1.0–1.5 parts, and stearic acid lubricant at 0.5–1.0 part. The paste is mixed under vacuum at 5–10 kPa absolute pressure to remove air bubbles, then extruded through a single-screw or twin-screw vacuum extruder at a die pressure of 6–12 MPa. The high DP of the 088-60 grade increases green-body three-point bending strength to 3.5–6.0 MPa at a moisture content of 12–18%, which is sufficient for thin-wall cellular structures with wall thickness down to 0.08–0.15 mm. Drying is staged at 40–60 °C for 24–48 h until moisture falls below 2.0%; rapid drying above 80 °C causes surface cracking because the high-viscosity binder traps water at the core. Debinding is performed in air or nitrogen at a heating rate of 0.5–1.0 °C/min to 450 °C with a hold of 1–2 h; oxygen-starved atmospheres can leave carbon residue from the high-molecular-weight PVA. Fired parts include automotive catalytic converter substrates and diesel particulate filter cores, where green strength and binder burnout are evaluated by ASTM C133-97 for modulus of rupture and thermogravimetric analysis under ISO 11358-1:2022. Published data for this specific Shuangxin grade in cordierite systems is limited; the numerical ranges above reflect production-scale extrusion practice with equivalent 26-88 PVA grades.
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Shuangxin 26-88 polyvinyl alcohol, also designated PVA 088-60, is a partially hydrolysed polyvinyl alcohol with a high nominal degree of polymerisation. The grade designation combines a polymerisation segment and a hydrolysis segment: 26 indicates a nominal degree of polymerisation of 2600, and 88 indicates a target hydrolysis level of 88 mol%. The export designation 088-60 encodes the same hydrolysis target and a nominal 4% aqueous solution viscosity of 60 mPa·s at 20 °C; the controlled specification for 26-88 is typically 55.0–65.0 mPa·s when measured according to GB/T 12010.3-2010.
The product is supplied as a white to off-white granular solid with a residual acetate content of 11.0–13.0 mol% corresponding to the hydrolysis range. It is used in high-viscosity aqueous adhesives, paper surface sizing, textile warp sizing, temporary film casting, and emulsion polymerisation as a protective colloid. The following lot-level specification profile is used for incoming quality control.
| Property | Controlled range | Method reference |
|---|---|---|
| Degree of hydrolysis | 87.0–89.0 mol% | GB/T 12010.2-2010 |
| Viscosity, 4% aqueous, 20 °C | 55.0–65.0 mPa·s | GB/T 12010.3-2010 |
| Residual acetate content | 11.0–13.0 mol% | calculated from saponification value |
| Volatile matter | ≤5.0 wt% | manufacturer certificate method |
| Ash | ≤0.5 wt% | manufacturer certificate method |
| pH, 4% aqueous solution | 5.0–7.5 | manufacturer certificate method |
The 26-segment corresponds to a nominal degree of polymerisation of 2600. For an 88 mol% hydrolysed polymer with 12 mol% residual vinyl acetate, the average repeat-unit mass is approximately 49.0 g/mol, giving a nominal molar mass near 1.27 × 105 g/mol. This molar mass is higher than that of 17-88 and 24-88 and contributes directly to higher aqueous solution viscosity, higher film tensile strength, and slower dissolution. The hydrolysis level of 88 mol% leaves enough residual acetate groups to disrupt interchain hydrogen bonding, reducing crystallite density and permitting cold-water dispersion at 20–35 °C. Fully hydrolysed 26-99 with the same nominal DP has a higher crystallinity and requires dissolution above 90 °C.
Degree of hydrolysis is measured after saponification under GB/T 12010.2-2010. The residual acetate range of 11.0–13.0 mol% can be used as an incoming lot check because it affects solubility, surface activity, and compatibility with plasticisers.
In cast film and temporary protective film use, 26-88 exhibits a higher tensile strength and lower elongation than lower-DP 17-88. Published PVOH film data for 88 mol% grades conditioned at 23 °C and 50 ± 5% RH under ISO 291 place tensile strength in the range of 55–70 MPa and elongation at break in the range of 100–200% when tested in accordance with ASTM D882-18; published data for this specific 26-88 configuration is limited, so internal film testing at 100 μm dry thickness is recommended. Fully hydrolysed 26-99 with a similar DP can exceed 80 MPa but shows lower elongation and requires hot-water processing.
At relative humidity above 60%, moisture uptake in 88 mol% PVOH films reduces tensile strength and glass transition temperature. The material is not suitable for continuous water immersion unless crosslinked with boric acid, glyoxal, isocyanate, or a thermosetting resin; immersion performance must be verified by the end-use specification, typically via tensile retention after 24 h water soak at 23 °C in accordance with ASTM D882-18 or ISO 527-3.
Aqueous preparation of 26-88 is normally performed by cold-water dispersion at 20–35 °C before heating to 85–95 °C. Direct addition of dry powder to hot water produces surface gelation and floating agglomerates. A jacketed stainless steel tank with a baffled turbine is preferred; high-shear rotor-stator devices are not required for dissolution and can introduce excessive air. For a 10 wt% stock solution, filtration through an 80–120 mesh filter is common to remove undissolved gel bodies. Because the 4% solution viscosity is 55.0–65.0 mPa·s, positive-displacement or diaphragm pumps are preferred over centrifugal pumps, and recirculation-loop backpressure should not exceed 2.0 bar to limit shear heating. Direct steam injection into concentrated solution should be avoided because local temperature overshoot above 90 °C can form gel skins and create visible defects in cast films.
In paper surface sizing, 26-88 is combined with starch-based size press formulations at 0.5–3.0 wt% of sizing solids. The high molecular weight improves surface tensile strength and reduces Cobb water absorption; Cobb values are measured according to TAPPI T 441. The required addition level is controlled by sheet ash, starch viscosity, and size press pickup. For remoistening adhesives in labels and paper converting, 26-88 contributes high initial tack and improved shear resistance after drying. Open time is shorter than with 17-88; plasticisers such as glycerol or sorbitol at 5–15% of dry PVOH are typically added to extend open time. Brookfield viscosity is monitored at 25 °C by ISO 2555:2018 to maintain coating uniformity.
In vinyl acetate-ethylene emulsion polymerisation, 26-88 acts as a protective colloid. A high-DP protective colloid raises the aqueous-phase viscosity and can shift latex particle size distribution; the final latex viscosity at 55% solids may exceed 10,000 mPa·s when measured by ISO 2555:2018, depending on initiator level and monomer feed profile. Production-scale reactors with top-entering impellers may require a torque increase when the PVOH charge shifts from 17-88 to 26-88; published data for this specific product is limited, so pilot-scale agitation power is recommended before full substitution.
Replacing 17-88 with 26-88 at equal solids raises the 4% aqueous solution viscosity from 20.0–26.0 mPa·s to 55.0–65.0 mPa·s, an increase of approximately 2.5–3.0 times. For a fixed coating viscosity and positive-displacement feed, the solids of a 17-88 formulation must be reduced or the pump speed lowered to maintain the same pressure drop. In textile warp sizing, upper-viscosity lots at 65 mPa·s may require size-box solids reduction of 0.3–0.8 wt% to prevent size trough skinning and foam in high-speed beam warping; published data for this specific product is limited. Hydration time for stock solutions should be extended from approximately 30 min to 60–90 min at 90 °C when moving from 17-88 to 26-88.
The performance difference is also evidenced in film tensile strength and adhesive shear. The following comparison is based on typical 88 mol% PVOH grade data and should be confirmed against lot certificates.
| Grade | 4% viscosity at 20 °C | Hydrolysis range | Processing/performance distinction |
|---|---|---|---|
| 17-88 | 20.0–26.0 mPa·s | 87.0–89.0 mol% | Low viscosity; fast dissolution; lower film tensile strength; used in low-solids adhesives and spray-dried powders |
| 24-88 | 44.0–52.0 mPa·s | 87.0–89.0 mol% | Intermediate viscosity; balanced handling and film strength; used in medium-viscosity adhesives and surface sizing |
| 26-88 | 55.0–65.0 mPa·s | 87.0–89.0 mol% | High viscosity and film strength; slower dissolution; used in high-strength adhesives, warp sizing, and temporary films |
| 26-99 | 55.0–65.0 mPa·s | 99.0–99.8 mol% | Hot-water soluble; higher tensile and water resistance; lower flexibility; requires dissolution above 90 °C |
For food-contact packaging, the use of 26-88 must be evaluated in the finished formulation under FDA 21 CFR 175.105, 176.170, or 176.180 as applicable. The resin alone does not confer food-contact approval. Under EU REACH, polyvinyl alcohol is a registered polymer; the lot certificate should be checked for vinyl acetate monomer and methanol residuals if the product is used in printing or medical packaging. Pre-drying before hot processing should be performed when storage relative humidity exceeds 60% because moisture uptake can affect film clarity and melt processing.