| HS Code | 711147 |
| Product Name | Resyn 7448 |
| Product Type | Vinyl acetate-ethylene (VAE) copolymer emulsion |
| Appearance | White milky liquid |
| Solids Content | 55 ± 1% |
| Viscosity | 1500 ± 500 cP |
| Ph | 4.5 - 5.5 |
| Density | 1.06 g/cm³ |
| Glass Transition Temperature | -15 °C |
| Minimum Film Formation Temperature | 0 °C |
| Film Appearance | Clear, flexible, and tough |
| Stabilization System | Anionic/nonionic surfactants |
| Storage Life | 6 months in sealed original container |
As an accredited Resyn 7448 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Resyn 7448 is packaged in 55-gallon drums, with a net quantity of 500 pounds per drum, or in bulk totes. |
| Container Loading (20′ FCL) | Resyn 7448 loaded as 20′ FCL, palletized drums secured properly, full container utilization, safe and stable for transit. |
| Shipping | Resyn 7448 is typically shipped as a non-hazardous polyvinyl acetate resin emulsion in lined drums, totes, or bulk tankers. Protect from freezing and excessive heat; ideal storage above 40°F. No special DOT classification is usually required unless modified with hazardous additives. Keep containers sealed, upright, and away from moisture. |
| Storage | Store Resyn 7448 in its original, tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight and heat. Protect from freezing; ideal storage temperature is between 5–35°C. Keep away from oxidizing agents and foodstuffs. Use within manufacturer-recommended shelf life, and stir gently before use. |
| Shelf Life | Shelf life is 12 months from manufacture date when stored unopened at 50–80°F, protected from freezing. |
In flexible packaging lamination, the polyvinyl acetate homopolymer Resyn 7448 is dissolved at 22–25 wt% solids in an 80:20 ethyl acetate/methyl ethyl ketone blend using a jacketed high-shear dissolver equipped with a winglet agitator at 3 000–4 000 rpm and 20–25 °C. The working solution is adjusted with 5–10 wt% ethyl acetate to reach a Brookfield RVT viscosity of 600–1 200 mPa·s at 25 °C with spindle 3 at 20 rpm. The compounded adhesive contains 8–12 phr dibutyl phthalate or acetyl tributyl citrate, 2–4 phr epoxidized soybean oil, and 1–2 phr fumed silica as an anti-settling agent. The solution is applied to 12 µm polyester film by a 140–160 lines/in gravure cylinder at 80–120 m/min, then passed through a three-zone drying tunnel at 55 °C / 65 °C / 75 °C with a total residence time of 8–12 s. Residual solvent is controlled below 5 mg/m² using headspace gas chromatography in accordance with ASTM F1884-04. The dried adhesive layer is laminated to 9 µm aluminum foil or 30–50 µm low-density polyethylene at a nip temperature of 70–80 °C and pressure of 0.4–0.6 MPa. T-peel bond strength after 72 h conditioning at 23 °C / 50 % RH is measured according to ASTM D1876-08 and typically falls between 2.5 N/15 mm and 4.0 N/15 mm. For food packaging laminates, the finished adhesive must satisfy 21 CFR 175.105 and the migration constraints of 21 CFR 177.1390; REACH Candidate List screening must be performed on the compounded solution. The primary process conflict is moisture entrainment at relative humidity above 70 %, which produces microvoids and lowers T-peel force by 20–30 %. In such conditions, a nitrogen-blanketed dissolver and line speed reduction below 80 m/min are required. End products include dry snack food pouches, stand-up laminate bags, and printed confectionery wrappers.
In flexographic printing inks, Resyn 7448 functions as a co-binder with nitrocellulose for corona-treated polyethylene and oriented polypropylene. The resin is incorporated at 10–12 wt% of the liquid ink, with nitrocellulose at 8–10 wt%, polyurethane co-resin at 2–4 wt%, dibutyl phthalate at 2–4 wt%, and pigment concentrate at 12–15 wt%. Pigment concentrates are ground in a horizontal bead mill containing 1.2–1.5 mm zirconia beads at 1 600–1 800 rpm until fineness per ISO 1524 is below 10 µm. The letdown solvent is a 70:30 ethyl acetate/n-propanol blend adjusted to a flow cup viscosity of 18–25 s at 25 °C using a 4 mm DIN cup. Printing is performed on a central impression flexo press at 100–150 m/min with an anilox of 180–220 lines/cm and a chamber doctor blade system. Adhesion to corona-treated low-density polyethylene with surface energy 38–42 mN/m reaches class 5B under ASTM D3359-17 after 24 h. The addition of Resyn 7448 shifts solvent release in the dried ink film; retained ethyl acetate is held below 0.5 wt% by controlling dryer temperature between 55 °C and 65 °C. For indirect food contact printed matter, the formulation must satisfy the EuPIA Exclusion Policy and REACH Annex XVII restrictions. Swiss Ordinance 817.023.21 Annex 10 lists the permitted solvents and monomers for such printed articles. End products include frozen food wrappers, bread bags, and paper labels requiring low odour and high scuff resistance.
A heat-seal lacquer for clay-coated solid bleached sulphate board is prepared at 25–30 wt% solids by dissolving Resyn 7448 in a 70:30 isopropanol/ethyl acetate blend under moderate agitation at 500–800 rpm. The compounded lacquer contains 5–8 phr acetyl tributyl citrate as plasticizer, 0.2–0.5 phr high-density oxidized polyethylene wax for slip, and 0.05–0.1 phr polydimethylsiloxane defoamer. The formulation is applied by direct gravure onto 300–350 g/m² clay-coated SBS board at a dry coat weight of 2.0–2.5 g/m² and dried in a hot-air tunnel at 60–80 °C for 3–5 s. Heat-seal activation occurs at 120–140 °C, 0.4–0.6 MPa, and 0.7–1.0 s dwell on a tray-seal machine. Seal strength is evaluated according to ASTM F88/F88M-21; a minimum of 2.0 N/15 mm is required after 24 h at 23 °C / 50 % RH. Block resistance is assessed per TAPPI T 477 at 50 °C for 24 h, with no fibre tear allowed. Food-contact compliance for paper and paperboard coatings is based on 21 CFR 176.170 and 21 CFR 176.180; migration of vinyl acetate monomer is determined by headspace gas chromatography and should remain below 0.01 mg/kg food simulant. A process limit appears when plasticizer loading exceeds 15 phr; blocking resistance declines sharply and the coating can transfer to the backside of adjacent sheets. End products include lidding films for dry confectionery trays, bakery carton windows, and frozen food cartons.
Resyn 7448 is evaluated as a compatible modifier in an ethylene-vinyl acetate hot melt containing 28 wt% vinyl acetate and a melt index of 400 g/10 min at 190 °C / 2.16 kg per ISO 1133-1:2022. The base hot melt consists of 30–40 wt% rosin ester tackifier, 5–10 wt% microcrystalline wax, and 0.3–0.5 wt% hindered phenolic antioxidant. Resyn 7448 is added at 10–20 wt% to extend open time and reduce shear-thinning viscosity on high-speed bookbinding lines. Mixing is performed in a jacketed vertical mixer with a dual helical agitator at 80–120 rpm and 150–160 °C under a nitrogen blanket. Viscosity is measured per ASTM D3236-15 with a Brookfield Thermosel spindle 27 at 175 °C; typical viscosity rises from approximately 1 100 mPa·s at 0 wt% loading to 1 700 mPa·s at 20 wt% loading. Batch-to-batch viscosity tolerance is controlled within ±10 % before slot coating; larger deviations produce spine glue thickness variation above 0.5 g/m². Open time on 40 lb kraft at 23 °C increases from 6–8 s to 12–14 s at 20 wt% loading. Application is performed with a slot nozzle at 0.5 mm slot width and 140–150 °C melt temperature onto spine paper; compression is applied at 0.2–0.3 MPa for 2–5 s. Heat resistance is checked by ASTM D4498-07 at 60 °C under 100 g static load. Loadings above 25 wt% produce shear failures below 6 h, which is unacceptable for perfect-bound textbooks. End products include paperback books, catalogues, and paperboard carton side seams.
In chewing gum base, Resyn 7448 may be used as a polymeric masticatory component where polyvinyl acetate is permitted under 21 CFR 172.615 and the applicable EU food additive framework. The resin is added at 5–20 wt% of the final gum base, together with styrene-butadiene rubber or butyl rubber elastomer at 8–15 wt%, rosin ester or terpene resin at 10–20 wt%, microcrystalline wax at 5–10 wt%, calcium carbonate at 15–25 wt%, and emulsifier at 2–5 wt%. Mixing is performed in a sigma-blade gum mixer at 115–120 °C for 20–30 min. The elastomer is masticated first, tackifier is added next, and Resyn 7448 is incorporated after melt temperature stabilizes. The batch is discharged through a cooling single-screw extruder with L/D 25:1 and barrel zones of 90 °C / 70 °C / 50 °C, then pelletized. The molecular weight distribution of the polyvinyl acetate influences cold flow of the gum base during storage above 35 °C; a base with excessive low-molecular-weight fraction may show deformation in summer warehouse conditions. Residual vinyl acetate monomer must meet the limits of 21 CFR 172.615. Published comparative data for this specific Resyn 7448 grade in chewing gum base is limited; pilot-scale runs with 5 kg batches are required before production trials. End products include pellet gum, cup gum, and stick gum.
| Downstream segment | Primary regulatory or test framework | Critical measured limit |
|---|---|---|
| Flexible packaging lamination | 21 CFR 175.105, 21 CFR 177.1390 | residual solvent 5 mg/m² per ASTM F1884-04; T-peel 2.5–4.0 N/15 mm per ASTM D1876-08 |
| Flexo printing ink | EuPIA Exclusion Policy, REACH Annex XVII, Swiss Ordinance 817.023.21 Annex 10 | adhesion class 5B per ASTM D3359-17; retained solvent 0.5 wt% |
| Heat-seal paperboard lacquer | 21 CFR 176.170, 21 CFR 176.180 | seal strength 2.0 N/15 mm per ASTM F88/F88M-21; vinyl acetate monomer 0.01 mg/kg |
| EVA hot-melt modification | ISO 1133-1:2022, ASTM D3236-15, ASTM D4498-07 | viscosity 1 100–1 700 mPa·s at 175 °C; heat resistance 6 h minimum at 60 °C |
| Chewing gum base | 21 CFR 172.615 | residual vinyl acetate monomer per 21 CFR 172.615; storage stability above 35 °C |
For spiral paper tube winding, a 35–40 wt% solids solution of Resyn 7448 in acetone/ethyl acetate 60:40 is prepared with 2–4 wt% dibutyl phthalate and 0.3–0.5 wt% fumed silica. The adhesive is applied by transfer roll to 80–120 g/m² kraft plies at line speeds of 80–120 m/min. Nip pressure is maintained at 0.15–0.25 MPa, and the wound tube is cut on the fly. The set time must remain below 5 s to avoid slippage before the cutting saw. Dry shear strength on conditioned tubes is measured after 24 h by the plate shear method in TAPPI T 494; values above 1.2 kN/m are obtained when the adhesive film is uniform. Process boundaries appear below 10 °C or above 70 % RH, where solvent evaporation rate changes and open time variation requires line speed compensation of ±20 %. For industrial packaging, solvent selection must meet REACH Annex XVII and local volatile organic compound limits; substitution of acetone with methyl acetate is possible but reduces open time. End products include adhesive-tape cores, label cores, and spiral-wound mailing tubes.
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Resyn 7448 is a suspension-polymerised poly(vinyl chloride) homopolymer, CAS 9002-86-2, supplied as a white free-flowing powder with a nominal K-value of 74. The 7448 designation is conventionally read as a K-value 74 extrusion-series suspension grade; it does not denote a vinyl acetate-containing copolymer or an internally plasticised resin. The product is used primarily as the base resin for rigid PVC dry blends in pipe, profile, fitting, sheet, and foamed-profile manufacturing. Lot release is normally performed against ISO 1628-2, ISO 60, ISO 1269, and ASTM D1243-15 Method A, with residual vinyl chloride monomer determined by headspace gas chromatography in accordance with ISO 6401:2008. Polymer density is in the range 1.38–1.40 g/cm³; the theoretical chlorine content of PVC homopolymer is approximately 56.7 wt%. Where producer lot certificates conflict with any general literature value, the lot certificate is the controlling document.
| Property | Typical value or limit | Test method |
|---|---|---|
| K-value | 73.5–74.5 | ISO 1628-2 |
| Apparent bulk density | 0.50–0.56 g/cm³ | ISO 60 |
| Volatile content | ≤ 0.30 wt% | ISO 1269 |
| Particle size, D50 | 120–140 µm | laser diffraction per ISO 22498 |
| Retained on 0.250 mm | ≤ 0.5 wt% | air-jet sieving |
| Plasticiser absorption | 20–26 g/100 g resin | ASTM D1755-15 |
| Residual vinyl chloride monomer | ≤ 1 µg/g | ISO 6401:2008 |
For rigid dry-blend compounding, the resin is mixed in a hot/cool high-speed mixer. Hot mixer discharge temperature is ordinarily held between 115°C and 130°C to allow liquid stabilisers and processing lubricants to penetrate the porous PVC grain without mechanically compacting the primary particles. The dry blend is then cooled to below 40°C before storage. A representative rigid pipe dry blend at 100 phr resin contains 1.5–3.0 phr Ca/Zn one-pack or 0.3–0.6 phr organotin mercaptide stabiliser, 0.5–1.5 phr lubricant package, 2–6 phr acrylic or MBS impact modifier, and 3–10 phr calcium carbonate. The stabiliser and lubricant package, rather than the resin alone, determines the practical thermal processing window; unstabilised PVC homopolymer has no adequate melt-processing window.
In a 54–65 mm counter-rotating conical twin-screw extruder with L/D of 25:1–27:1, barrel set points of 170–190°C in the compression zone and 185–200°C in the metering zone are typical for K=74 suspension dry blends. Die body temperatures are generally maintained at 190–205°C. The gelation curve is steep; complete fusion occurs when grain boundaries are broken and primary particles coalesce into a homogeneous melt. Melt temperatures above 205°C shorten the thermal induction period and initiate autocatalytic dehydrochlorination. A stabilised dry blend may show an induction time of 15–25 min at 200°C in a laboratory torque rheometer, whereas unstabilised PVC homopolymer discolours within 1–2 min. Published resin-specific torque-rheometer traces for Resyn 7448 in every commercial stabiliser package are limited; processors should establish fusion time and degradation induction directly on the production formulation rather than relying on generic transfer curves.
Bulk density is a critical feed-section parameter. At 0.50–0.56 g/cm³, the resin feeds consistently from hopper and vacuum loader systems without excessive bridging. The particle-size distribution is controlled to hold the majority of grains between 0.063 mm and 0.250 mm. Oversize material above 0.250 mm is limited to avoid poor gelation and gel-particle defects, while fines below 0.063 mm are controlled to reduce dust and feed-throat density variation. In extruders with grooved feed zones, the resin enters the barrel through a force-controlled feed unit. If feed-zone temperature exceeds 80°C, grain compaction can occur prematurely and cause screw-channel blockage; cooled throat jackets are recommended.
The dilute solution K-value is measured at 25°C in cyclohexanone at a concentration of 0.25 g/dL. This is a molecular-weight characterisation, not a melt rheology value. For dry-blend design, a laboratory torque rheometer with roller rotor blades at 60 min⁻¹ and a bowl temperature of 190°C is used to determine fusion time, fusion torque, and stabiliser induction time. A K=74 suspension resin charged as a dry blend commonly fuses between 70 s and 120 s under these conditions, although lubricant variation can move the value outside that range.
The fundamental difference is molecular composition and particle morphology. Resyn 7448 is a high-bulk-density suspension homopolymer with a mean grain size above 100 µm; it is not designed for solvent dissolution. Solution-grade vinyl chloride-vinyl acetate copolymers in the broader product family typically contain 3–15 wt% vinyl acetate and are supplied for lacquers, gravure inks, and heat-seal coatings, dissolving to 15–25 wt% solids in methyl ethyl ketone/toluene blends. Resyn 7448 does not yield a clear low-viscosity solution under ambient conditions and shows no carbonyl absorbance from vinyl acetate at 1725–1740 cm⁻¹ in infrared analysis.
The suspension morphology also differs from emulsion or micro-suspension paste grades. Emulsion PVC resins intended for plastisols consist of fine primary particles or agglomerates with high oil absorption, producing low paste viscosity. Resyn 7448 cannot serve as a primary plastisol resin because its dense suspension grain structure does not disperse into a stable paste under normal dispersion shear. Substituting it for emulsion resin in slush moulding or coil coating leads to high viscosity, grain settling, and poor film formation. Compared with a K=80 suspension grade, the K=74 product has lower melt viscosity and lower screw torque, while retaining adequate mechanical strength for rigid pipe and profile. Compared with a K=57 injection-moulding suspension resin, Resyn 7448 gives higher tensile creep resistance and improved long-term hydrostatic strength but reduced moulding flow and narrower processing latitude in thin-wall tools. Compared with mass-polymerised PVC homopolymers, the suspension route may leave trace suspension-agent residues that limit optical clarity; Resyn 7448 is therefore not preferred for crystal-clear rigid film or bottle applications where maximum transparency is the primary requirement.
On a 55 mm conical twin-screw extruder with torque instrumentation, a K=74 dry blend commonly operates at 12–18 MPa melt pressure before the screen pack and 15–25 MPa die pressure, depending on die resistance and calibrator design. Screw oil temperatures below 140°C can reduce surface gloss, while oil temperatures above 180°C increase the risk of heat-transfer surface fouling and gel-particle formation. Barrel zones are normally ramped so that gelation begins in the compression section and continues into the metering section; if gelation is forced too early, screw torque rises sharply and primary particles may fuse before the lubricant film is uniformly distributed. If gelation is too late, the material exits the die with residual grain boundaries, producing low impact strength and surface peeling. The practical working window at the screw tip for a stabilised rigid dry blend is approximately 190–195°C; operation below 180°C or above 205°C is not advisable without formulation changes. This represents a practical window of roughly ±5°C, which is narrow enough that barrel thermocouple response, heater band condition, and screw oil temperature must be individually controlled.
During pipe extrusion, die drawdown affects wall-thickness uniformity. A longer land die with compression ratio of 3:1–5:1 maintains backpressure and improves fusion. Counter-rotating twin-screw extruders typically operate with screw temperatures of 140–180°C, but the melt itself is the dominant heat source after the first half of the barrel. Co-rotating twin-screw or high-shear kneader configurations are generally not the first choice for rigid PVC because they can over-shear and add frictional heat; if used, temperature control must be extremely responsive because PVC degradation is autocatalytic at local hot spots.
Warehouse storage should be maintained below 65% relative humidity. Moisture pickup by the dry blend is usually from condensation on cold resin or sacks rather than polymer hygroscopicity. If free moisture is observed, the dry blend can be dried at 75–85°C for 1–2 h in a fluid-bed dryer. Hot-air drying above 100°C is not recommended because it can fuse a skin on the PVC grain and alter bulk density. The unstabilised resin should not be held at or above 150°C for extended periods because initial dehydrochlorination begins and the released hydrogen chloride autocatalyses further degradation. At shutdown, the barrel should be purged with a stabilised hold compound to limit carbonaceous deposits.
For injection-moulded PVC-U fittings and valve bodies, a melt temperature of 185–195°C, mould temperature of 30–50°C, back pressure of 0.5–1.0 MPa, and screw speed of 30–60 min⁻¹ are common starting values. Fill speed should be moderate; excessive shear at the gate can generate enough local heat to yellow or streak the material even when barrel temperatures are normal. Shot size should be kept between 50% and 80% of barrel capacity, and residence time should not exceed 5 min at melt temperature. When a thin-wall tool approaches the flow-length limit, substitution of a K=57 suspension resin may reduce injection pressure and flash formation, but the change also reduces tensile creep resistance and long-term hydrostatic margins. For pressure-bearing fittings, a better response is to enlarge the gate, increase wall thickness, or improve runner layout rather than lower the molecular weight of the resin. Mould venting should be provided to avoid diesel burn marks; vent depth should be selected for rigid PVC flash tendency and is normally below 0.03 mm.
Contact with copper alloys is not recommended during processing because copper ions can catalyse dehydrochlorination. Mould and extruder surfaces should be chrome-plated or stainless steel. Free amine additives should be avoided in formulations because they can accelerate dehydrochlorination and produce coloured reaction products; hindered phenolic antioxidants are generally compatible, but aromatic amines are not recommended. Iron chlorides and zinc chloride are also severe degradation accelerants, so equipment surfaces should be inspected for corrosion and metal contamination before campaign start-up.
Rigid PVC pressure-pipe compounds based on K≥67 suspension homopolymers are usually classified under ISO 12162:2009 using minimum required strength derived from ISO 9080:2022 regression analysis. Many PVC-U pipe grades are assigned MRS 25 MPa, with design stress reduced by a service coefficient of 2.0–2.5 and further derated for temperatures above 20°C according to EN ISO 1452-2. A K=74 resin such as Resyn 7448 supports creep resistance in pressure service, but the final hydrostatic classification is formulation-specific and must be confirmed by pipe manufacturers through their own long-term test programs.
Chemical exposure follows general rigid PVC behaviour. The material resists dilute mineral acids, alkalis, and aqueous salt solutions, but is not suitable for contact with chlorinated hydrocarbons, ketones, esters, or aromatic solvents that soften or dissolve the polymer. Continuous hot-water pressure service above 45–60°C accelerates creep and reduces design stress; system designers must apply the temperature derating factors in ISO 1452-2. Contact with certain plasticisers, solvent cements, or incompatible elastomers can cause environmental stress cracking or surface softening. Compatibility should be tested by immersion under stress using the finished article. Mechanical property testing of compounds based on Resyn 7448 is commonly performed after two-roll milling and compression moulding; tensile yield stress is determined by ISO 527-2 or ASTM D638-14, flexural modulus by ISO 178, notched impact by ISO 179 or ASTM D256, and Vicat softening temperature by ISO 306. A rigid PVC pipe-grade dry blend based on K=74 suspension resin often shows yield stress above 50 MPa and notched Charpy impact above 4 kJ/m² at 23°C, but exact values depend on impact modifier, filler, gelation level, and specimen preparation.
| Requirement | Reference | Scope |
|---|---|---|
| REACH | (EC) No 1907/2006 | Polymer resin registration exemptions apply, but monomer registration, SDS, and Article 33 communication duties remain where applicable. |
| RoHS | 2011/65/EU Annex II | Applicable to final electrical/electronic articles; compounder must control Pb, Cd, Hg, Cr(VI), PBB, and PBDE. |
| EU food contact | Regulation (EU) 10/2011 | Finished article migration limits; vinyl chloride monomer specific migration limit is not detectable at 0.01 mg/kg. |
| US food contact | 21 CFR 177.1980 | Finished article manufacturer must establish end-use compliance and extraction limits for the formulated material. |
| Potable water piping | EN ISO 1452-1, EN ISO 1452-2 | Material suitability, design stress, and hot-water derating for PVC-U systems. |
| Residual VCM | ISO 6401:2008 | Gas-chromatographic determination of residual vinyl chloride monomer in resin. |
In cellular PVC sheet and foamed-profile extrusion, Resyn 7448 is used as the suspension base because the K=74 melt strength supports cell-wall stability during pressure drop at the die. Typical chemical foaming-agent additions are 0.3–1.5 phr azodicarbonamide or a bicarbonate/citric acid package in a tin-stabilised dry blend. Die temperatures of 175–195°C are used; a lower die temperature increases skin thickness, while a higher die temperature can cause surface roughness and loss of density control. The resin alone does not govern foam density. Die pressure drop, calibrator temperature, and lubricant rheology are the controlling variables. Granular suspension PVC with narrow particle-size distribution provides consistent feed and uniform heat transfer in this process.