| HS Code | 955292 |
| Product | Asrene LLDPE UF1820S1 |
| Density | 0.918 g/cm³ |
| Melt Flow Rate | 2.0 g/10min (190°C, 2.16kg) |
| Tensile Strength At Yield | 12 MPa |
| Tensile Strength At Break | 35 MPa |
| Elongation At Break | 750% |
| Vicat Softening Point | 102 °C |
| Melting Point | 122 °C |
| Dart Drop Impact | 120 g |
| Haze | 14% |
| Gloss | 10 |
As an accredited Asrene LLDPE UF1820S1 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Asrene LLDPE UF1820S1 is supplied in 25 kg net polyethylene bags, palletized and stretch-wrapped for safe handling and transport. |
| Container Loading (20′ FCL) | 20′ FCL of Asrene LLDPE UF1820S1, linear low-density polyethylene resin, packed in 25kg bags, shrink-wrapped on pallets. |
| Shipping | Ship Asrene LLDPE UF1820S1 in sealed, moisture-proof bags or containers to prevent contamination. Keep dry and store away from heat, ignition sources, and direct sunlight. Transport in clean, covered vehicles or containers. No special hazard classification expected, but avoid dust accumulation and follow standard material handling practices. |
| Storage | Store Asrene LLDPE UF1820S1 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep packaging sealed to prevent moisture pickup, dust contamination, and physical damage. Avoid prolonged outdoor storage or high stacking that could crush bags. No special hazardous storage requirements apply under normal conditions. |
| Shelf Life | Asrene LLDPE UF1820S1 has a shelf life of at least one year when stored in a cool, dry, shaded area away from direct sunlight and heat. |
A 45–65 mm barrier-screw blown-film line processing Asrene LLDPE UF1820S1 is typically operated at a melt temperature of 190–205 °C through a 1.8–2.0 mm die gap and a blow-up ratio of 2.2:1–3.0:1 for 18–25 µm packaging film. The resin has a nominal density of 0.918 g/cm³ under ASTM D792-20 and a melt flow rate of 2.0 g/10 min under ISO 1133-1:2022, which permits thin-gauge drawdown but limits low-melt-strength bubble sag if the frost line is raised beyond stable bounds. On production-scale machines, the dominant failure mode at these gauges is asymmetric frost-line height and diameter fluctuation rather than sharkskin; stabilization is achieved by holding the frost line at 390–480 mm above the die face and supplying internal bubble cooling air at 8–12 °C. Die pressure on grooved-feed extruders commonly falls between 150 bar and 200 bar for this density class, and a drop below 130 bar indicates feed starvation or screw wear. When the automatic air ring maintains bubble diameter to ±2 mm, circumferential gauge variation measured by ASTM D6988-21 typically stays below ±8%. Haze is evaluated by ASTM D1003-21 and gloss at 60° by ASTM D2457-21; commercial thin-gauge butene LLDPE of this density generally targets haze below 15% at 25 µm, but the exact UF1820S1 value must be checked against the certificate of analysis. For indirect food-contact packaging, compliance screening depends on FDA 21 CFR 177.1520 and Regulation (EU) No 10/2011; migration limits vary according to food simulant and film thickness, so a laminate-specific extraction test is required before use in high-temperature or fatty food contact.
For industrial sacks, liner films and carrier bags, UF1820S1 is extruded at 80–160 µm with a die gap of 2.2–2.5 mm and a blow-up ratio of 1.8:1–2.5:1. The lower blow-up ratio is selected to favour machine-direction tensile strength and film flatness, but it creates a measurable tear anisotropy: under ASTM D1922-15, Elmendorf tear values are typically higher in transverse direction than machine direction, and raising blow-up ratio from 2.0:1 to 2.8:1 can shift the balance by 10–25%. Dart impact is tested by ASTM D1709-16a using Method A for thinner webs and Method B for heavy webs; sack specifications in the 100 µm range commonly set a minimum dart impact of 300 g, but actual UF1820S1 values must be confirmed from production samples. Puncture resistance by ASTM D5748-19 is used as a secondary check for sharp packaged goods, because dart impact alone does not predict slow-puncture failure on angular regrind or irregular waste loads. Regrind addition is the most critical process variable: above 30 wt% regrind, the accumulation of oxidised gel particles and loss of slip/antiblock consistency can reduce dart impact and destabilize the bubble; inline melt-pressure and back-pressure monitoring are recommended, and the regrind fraction should be homogenized or conditioned if storage humidity exceeds 80%. A 65 mm extruder with a 200 mm die is typically run at 80–110 rpm and melt temperature 205–230 °C; output is limited by tower height and air-ring cooling rather than screw plasticising capacity. Surface moisture streaks from condensation in high-humidity warehouses are prevented by hopper heating at 50–60 °C; pre-drying is unnecessary for neat resin but is advised if the resin has been cold-warehouse stored and RH exceeds 80%. Published data specific to UF1820S1 under these regrind and thickness conditions is limited, so production validation is required before fixing lot-release thresholds.
The narrow heat-seal window and blocking tendency of 0.918 g/cm³ butene LLDPE define the operating limits of lamination sealant webs. Film of 15–30 µm is corona treated to at least 38 mN/m under ASTM D2578, and then bonded through solvent-based or solvent-free adhesive to PET, BOPP or metallized OPP. Heat seal strength is measured by ASTM F88/F88M-21 at jaw temperatures from 95 °C to 150 °C; butene LLDPE of this density usually shows seal initiation between 95 °C and 110 °C, with a stable plateau from 115 °C to 135 °C. Hot tack is measured by ASTM F1921-18 because vertical form-fill-seal lines require the seal to survive immediate product loading; for this density class, hot tack typically peaks between 110 °C and 125 °C. Above 150 °C, edge curl and squeeze-out increase, and machine-direction shrink can exceed 2%, causing misregistration on pre-printed webs. The coefficient of friction is screened by ASTM D1894; if UF1820S1 is the slip/antiblock-modified variant, kinetic COF should remain between 0.15 and 0.35 to avoid blocking during roll handling while maintaining sufficient pouch-machine tracking. Corona-treated surface energy decays with storage time; a treated web stored for 30 days at 23 °C can fall below 36 mN/m, so lamination should be scheduled within that window or inline re-corona should be used. Because the sealant is not the only migrant source in a finished laminate, overall migration must be tested with the intended food simulant under Regulation (EU) No 10/2011 or the applicable national hygiene standard.
In greenhouse and silage film, UF1820S1 requires modification because neat butene LLDPE alone does not provide sufficient environmental stress-cracking resistance or UV life. A starting coextrusion formulation consists of 70–80 wt% UF1820S1, 15–25 wt% LDPE and 5 wt% EVA, with a HALS/UV masterbatch dosed between 3 wt% and 7 wt% for 120–200 µm cladding film. The dosage is intensity-dependent: sites receiving annual UV energy above 500 MJ/m² generally require at least 150 µm nominal thickness and a higher HALS loading to keep tensile strength loss below 20% after 12 months under ISO 4892-2 or ASTM G154-23 accelerated cycles. ESCR is measured by ASTM D1693-21 Condition B; greenhouse specifications often require F50 above 400 h, and unmodified UF1820S1 may not meet that threshold, which is why LDPE or EVA modification is used. Processing on a blown-film line uses a die gap of 2.0–2.6 mm, blow-up ratio of 2.0:1–2.8:1, and melt temperature of 195–215 °C; the frost line is held higher than in thin packaging film because the thick bubble requires longer cooling residence time. EVA levels above 10 wt% reduce thermal stability and increase tack, so screw speed is adjusted to keep melt temperature below 220 °C and to avoid degradation of the EVA fraction. In high-altitude sites with high UV and rapid night cooling, condensation on the film interior is a separate failure mechanism; anti-drip additives are used only after checking compatibility with the HALS package. Published data specific to UF1820S1 in long-term cladding applications is limited, so site-specific exposure trials are required before writing multi-season warranties.
If UF1820S1 is used as a 20–30 wt% let-down in collation shrink film, the blown film is produced at 40–80 µm with a die gap of 1.8–2.2 mm, blow-up ratio of 1.8:1–2.2:1, and die temperature of 200–215 °C. Shrink properties are measured in a hot-air tunnel at 150 °C using ISO 14616:1997; LDPE-rich films of this configuration typically show machine-direction free shrink of 55–75% and transverse-direction free shrink of 35–60%, while the UF1820S1 fraction reduces shrink but improves puncture and seal robustness. Shrink force is measured by ASTM D2838-18; when the UF1820S1 content exceeds 40 wt%, shrink force often falls below 0.6 N/cm, which is inadequate for bundling heavy multi-pack loads. Web flatness is maintained with a low frost line and a dual-lip air ring; insufficient airflow produces differential shrinkage that later appears as wavy cuts and torn shrink windows on high-speed collation lines. Slip/antiblock additives in UF1820S1 affect the stacking behaviour of shrink film; if the kinetic COF measured by ASTM D1894 drops below 0.10, roll telescoping increases, while values above 0.40 reduce machinability. Corona treatment above 38 mN/m is needed for printing but must be limited to avoid excessive surface oxidation that raises COF and promotes blocking during storage. Because shrink force and shrinkage are highly formulation-dependent, published data specific to UF1820S1 collation shrink blends is limited; pilot-line trials should establish the exact LDPE let-down and slip/antiblock balance before commercial runs.
For export screening of UF1820S1 film stock, the following standards are applied. The compliance burden is end-use-dependent and must be verified on the finished film or laminate, not solely on the raw resin certificate.
| Regulation / standard | Clause or test method | Application sector | Verification requirement |
|---|---|---|---|
| FDA 21 CFR 177.1520 | Olefin polymers, food-contact conditions A–H | Food packaging films, lamination sealant webs | Resin Statement of Compliance; finished-film extraction testing per food type |
| Regulation (EU) No 10/2011 | Annex I and Annex II, overall migration ≤ 10 mg/dm² | EU food-contact laminates | EU Declaration of Compliance; specific migration testing for additives |
| REACH Annex XVII | SVHC content ≤ 0.1 wt%; restricted substances | All export films | SDS screening, SVHC test report |
| RoHS Directive 2011/65/EU | Annex II: Pb, Hg, Cr VI, PBB, PBDE ≤ 1000 ppm; Cd ≤ 100 ppm | Industrial films supplied to EEE applications | XRF or ICP verification on finished film |
| ASTM D1238-23 / ISO 1133-1:2022 | MFR at 190 °C/2.16 kg | Incoming resin control | Certificate of analysis against product specification |
| ASTM D792-20 / ISO 1183-1:2019 | Density | All applications | Certificate of analysis |
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Asrene LLDPE UF1820S1 is a butene-comonomer linear low-density polyethylene supplied in pellet form for blown-film extrusion. The manufacturer identifies a nominal melt flow rate of 2.0 g/10 min at 190 °C/2.16 kg according to ASTM D1238/ISO 1133-1 and a nominal density of 0.918 g/cm³ according to ISO 1183-1/ASTM D792. The grade carries a formulated slip and antiblock system; exact slip-agent and antiblock loadings are lot-specific and are recorded on the certificate of analysis rather than in the standard datasheet. Typical values should not be construed as specification limits; the lot certificate governs.
| Property | Test method | Nominal value |
|---|---|---|
| Melt flow rate at 190 °C/2.16 kg | ASTM D1238 / ISO 1133-1 | 2.0 g/10 min |
| Density | ISO 1183-1 / ASTM D792 | 0.918 g/cm³ |
| Tensile stress at break on 40 µm film, MD/TD | ASTM D882 | 25–35 MPa / 20–30 MPa |
| Elongation at break on 40 µm film, MD/TD | ASTM D882 | 500–700% / 700–900% |
| Haze on 40 µm film | ASTM D1003 | 10–15% |
| Coefficient of friction, kinetic film-to-film | ASTM D1894 | 0.15–0.35 after maturation |
The values are representative of C4 LLDPE film of this melt index and density. Published data for this specific product configuration are limited to the supplier datasheet; production lots may differ. The certificate of analysis governs.
The melt flow rate of 2.0 g/10 min places UF1820S1 in the medium-molecular-weight C4 LLDPE class. At extrusion shear rates, the linear structure generates less extensional viscosity than high-pressure LDPE, so the bubble is less self-healing under air-ring fluctuations. The practical melt-temperature window on high-output lines is 190–210 °C; below 175 °C, melt pressure rises sharply and sharkskin may appear on the film surface. Above 230 °C, oxidative gel formation accelerates, particularly in the presence of residual oxygen from poorly purged hoppers.
Extruders with grooved feed sections and 24:1 to 30:1 L/D should run a barrel profile from 170–180 °C in the feed zone to 190–210 °C in the metering zone. Compression ratio is set between 2.8:1 and 3.5:1. A screen pack of 60/100 mesh is common; finer filtration increases head pressure and melt temperature. Die gap is usually 1.0–2.0 mm. At the 1.0 mm lower boundary, shear heating can add 5–10 °C to the melt temperature; extruder speed must be reduced if the melt approaches 220 °C. At the 2.0 mm upper boundary, the melt web is thicker, which can reduce gauge uniformity when combined with high blow-up ratios.
Blow-up ratio is controlled between 2.0:1 and 3.0:1, and frost line height is set to maintain bubble diameter within ±25 mm. Excessive cooling air creates a concave bubble neck and increases transverse shrinkage; insufficient cooling air raises the frost line and can destabilize the bubble at high screw speed. The lack of long-chain branching limits the self-stabilizing extensional hardening seen in LDPE, so automatic bubble guides are recommended for gauge control beyond 100 kg/h output on a 65 mm extruder.
At 190 °C and 100 s⁻¹, the apparent viscosity of this melt index class is lower than an MI 1.0 C4 LLDPE by approximately 20–30%, depending on molecular weight distribution. The critical shear rate for sharkskin in spiral mandrel dies is typically in the 500–1000 s⁻¹ range. Exceeding that rate without raising melt temperature produces visible surface roughness. Die-lip build-up from slip additives can accumulate over extended runs; periodic purging or fluoropolymer processing aids at 200–500 ppm is used on high-output lines to reduce the frequency of cleaning.
Pellets do not require pre-drying if stored sealed. At ambient relative humidity above 60%, condensation on cold pellets can cause bubble defects; a desiccant or hot-air hopper dryer at 60–70 °C for 2 h removes surface moisture. Blending with up to 20 wt% high-pressure LDPE improves bubble stability and melt strength, but reduces the dart impact advantage of the LLDPE. Blending with HDPE or polypropylene is not recommended because incompatible melts generate visible gels. Converters who compound their own slip or antiblock masterbatch should verify dispersion by measuring haze on 40 µm film and film-to-film coefficient of friction after 48 h.
The slip additive is a long-chain primary amide dispersed in the amorphous regions of the polyethylene. Migration to the film surface follows a concentration gradient and is strongly temperature-dependent. Immediately after extrusion, kinetic coefficient of friction measured by ASTM D1894 can exceed 0.50. After 24 h at 23 °C, the surface concentration rises enough to reduce COF below 0.35; after 72 h, it usually plateaus in the 0.15–0.30 range. Storage at 30–40 °C shortens the plateau time; storage below 5 °C slows migration and can leave film with high COF and blocking tendency. The inorganic antiblock, typically a synthetic silica with median particle size in the 3–5 µm range, creates microroughness that reduces film-to-film contact area.
Corona treatment raises surface energy to 38–42 mN/m for ink adhesion but oxidizes the surface amide layer, raising the measured coefficient of friction. Dyne solution checks are performed according to ASTM D2578; a reconditioning period of 24 h may be required before the slip bloom equilibrates after corona. In lamination-grade film, excessive slip can reduce bond strength to solventless polyurethane adhesives. The corona dose, adhesive chemistry, and maturation time should be evaluated on the treated surface rather than on untreated film. If the film is metallized, the slip package may outgas under vacuum; published data for this specific configuration is limited.
Blocking resistance in wound rolls is a function of contact pressure, temperature, and slip maturation. At roll pressures above 0.5 MPa, film-to-film adhesion increases if the slip bloom is incomplete. Rolls should be aged for 24 h before slitting at high tensions. Hot-climate storage above 40 °C accelerates slip migration but also softens the film; blocking may become worse if rolls are compressed. A two-stage winding profile with lower initial tension and step-up after 24 h reduces blocking defects.
Seal initiation for this butene LLDPE is not a fixed property; it depends on jaw pressure, dwell time, and film thickness. Under 0.5 s dwell and 0.3 MPa jaw pressure, initiation is typically 105–115 °C, which is 10–20 °C lower than a high-pressure LDPE of similar melt index. The hot-tack window measured by ASTM F1921 is broad enough for vertical form-fill-seal equipment; seal strength measured by ASTM F88 should be verified after 48 h of maturation because surface slip amides can act as a weak boundary layer before equilibration. The plateau seal temperature is usually below 160 °C; above this, the film thins excessively at the seal interface and loses burst strength.
The grade is not designed for solvent-based lamination requiring high-polarity anchor coatings without corona pretreatment. Aromatic solvents and strong oxidizers should be avoided because they can swell the polyethylene and extract surface additives. For food-contact use, the final film structure must be assessed under the intended simulant and contact ratio; the base polymer is typically covered by FDA 21 CFR §177.1520 and EU No 10/2011, but specific migration limits for the slip and antiblock additives must be confirmed with the supplier.
The butene comonomer introduces ethyl branches that are less efficient than hexene or octene branches at distributing short-chain branching. This lowers tie-chain concentration and reduces ultimate dart impact and tear resistance relative to hexene metallocene LLDPE of the same 0.918 g/cm³ density and 2.0 g/10 min melt index. In 40 µm film, dart impact measured by ASTM D1709 is typically lower by 15–30%, and Elmendorf tear measured by ASTM D1922 is lower in the machine direction. The optical haze is higher because of the additive package and the less regular crystallite structure.
Against high-pressure LDPE, the linear backbone gives higher tensile stress at break and higher puncture resistance at equal gauge. The lack of long-chain branching reduces melt strength; extrusion coating and cast-film drawing should be adjusted for greater neck-in and lower draw resonance. Against a C4 LLDPE of 1.0 g/10 min and the same density, UF1820S1 runs at lower head pressure and torque; the trade-off is slightly lower bubble stability and lower dart impact at high blow-up ratios. A converter whose line is torque-limited may prefer UF1820S1; a converter whose film must pass a high cold-drop impact specification may need the lower-MI or hexene grade.
Film property comparisons are meaningful only at equivalent blow-up ratio, frost line height, and gauge. Increasing blow-up ratio increases transverse orientation and can partially compensate for TD tear; decreasing blow-up ratio increases MD orientation and improves tensile strength but reduces dart impact. The orientation balance is also influenced by die gap; a narrower die gap at constant output increases shear and MD orientation.
The water-vapour transmission rate is moderate and thickness-dependent; it should be measured on the final structure according to ISO 15106-2 or ASTM F1249 because coextruded layers, pigmentation, and surface additives affect permeability. Polyethylene is not an oxygen or flavour barrier; oxygen-sensitive products require coextruded EVOH or polyamide layers. Published data for this specific configuration is limited, so end-use barrier specifications must be verified by measurement rather than by inference from density or melt index.
For direct food-contact packaging, the following compliance checks are normally requested from the resin supplier and downstream converters. The base polymer may comply with FDA 21 CFR §177.1520 and Commission Regulation (EU) No 10/2011, but the final film structure, inks, adhesives, and lamination layers must be evaluated separately. REACH and RoHS declarations are lot-specific and should be maintained in the technical file.
| Compliance area | Standard / regulation | Verification document |
|---|---|---|
| Olefin polymer food contact | FDA 21 CFR §177.1520 | Certificate of compliance |
| EU plastic food contact | EU No 10/2011 | Declaration of compliance |
| REACH SVHC | Regulation (EC) No 1907/2006 | Supplier statement |
| RoHS heavy metals | Directive 2011/65/EU | Supplier statement / XRF |
For less demanding dry blending or pellet handling, conventional hopper loaders and vacuum conveying systems suffice. No special pre-heating is required. Pellet dust is low, but long vacuum conveying distances can abrade pellets and generate fines that carry slip additive to the die lip; conveying velocity should be controlled below 25 m/s where possible.
On a 65 mm grooved-feed extruder with a 150 mm spiral mandrel die, a stable operating envelope is established with a die gap of 1.5 mm, blow-up ratio of 2.5:1, and frost line height of 250–350 mm. At 25–60 µm gauge, this geometry yields a balanced MD/TD orientation. High-speed form-fill-seal trials show that a kinetic coefficient of friction below 0.30 after 48 h of maturation is sufficient for reliable film path control; however, if the film is later corona treated for lamination, the coefficient of friction should be re-measured. For heavy-duty sacks, the resin can be used in coextruded structures where the core layer carries the mechanical load and the skin layer supplies slip and seal performance. The practical upper gauge limit is governed by the cooling rate of the bubble, not by the resin itself.