| HS Code | 475006 |
| Product Name | HANWHA LLDPE 3224 |
| Chemical Family | Linear Low-Density Polyethylene (LLDPE) |
| Density | 0.924 g/cm³ |
| Melt Flow Index | 2.0 g/10 min (190°C, 2.16 kg) |
| Melting Point | 122 °C |
| Vicat Softening Point | 100 °C |
| Tensile Strength At Yield | 12 MPa |
| Elongation At Break | 600 % |
| Flexural Modulus | 350 MPa |
| Shore Hardness D | 55 |
| Brittleness Temperature | -70 °C |
| Environmental Stress Crack Resistance | >500 hours |
As an accredited HANWHA LLDPE 3224 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | HANWHA LLDPE 3224 is packaged in 25 kg polyethylene bags, palletized and stretch-wrapped for safe handling, transport, and storage. |
| Container Loading (20′ FCL) | 20' FCL container loaded with HANWHA LLDPE 3224 pellets in 25kg bags, secured and stowed for safe transport. |
| Shipping | HANWHA LLDPE 3224 is a linear low-density polyethylene resin supplied as free-flowing pellets. For shipment, it is packed in 25 kg bags, jumbo bags, or available for bulk container transport. The material is non-hazardous, but should be kept dry, protected from moisture and direct heat during transit. |
| Storage | Store HANWHA LLDPE 3224 in a clean, dry, well-ventilated warehouse, away from direct sunlight, heat, and open flames. Keep original sealed bags intact to prevent moisture pickup, dust contamination, and physical damage. Avoid exposure to strong oxidizing agents. Maintain moderate temperatures below 50°C, stack bags securely, and use proper handling equipment to preserve resin quality. |
| Shelf Life | Shelf life is indefinite when stored in a cool, dry, well-ventilated area away from direct sunlight and heat. |
Monolayer blown film extrusion for heavy-duty sacks and industrial liners uses HANWHA LLDPE 3224 at a nominal melt flow rate of 2.0 g/10 min (ASTM D1238 / ISO 1133-1:2022, 190 °C, 2.16 kg) and a density of 0.920 g/cm³ (ASTM D1505 / ISO 1183-2). On a 65–90 mm grooved-feed extruder with an L/D of 25:1–30:1 and a spiral mandrel die of 200–300 mm diameter, the barrel profile is set from 150 °C at the feed throat to 195–205 °C at the adaptor, while the melt temperature measured in the die is kept between 195 °C and 210 °C. The compound is typically 100 phr LLDPE 3224, 1.0–2.5 phr slip/antiblock masterbatch, and 0.02–0.05 phr polymer processing aid. The die gap is maintained at 1.6–2.2 mm; reducing the gap below 1.4 mm raises melt pressure and can initiate sharkskin at high output, especially when the same die is run without process aid. Blow-up ratio is set at 2.2:1–2.8:1, with frost line height between 6 and 8 die diameters. Raising the frost line above 9 die diameters at ambient relative humidity below 40 % causes sustained bubble flapping on high-stalk lines, and the resulting gauge variation is measurable as an increase in thickness scatter under ISO 4593. Melt pressure at the screen changer is tracked; an increase above baseline by 50–70 bar indicates gel build-up on the screen pack, and a screen change is scheduled before film appearance defects become visible. Final film is tested for tensile properties under ISO 527-3 or ASTM D882, Elmendorf tear under ASTM D1922, dart drop impact under ASTM D1709 Method A, and coefficient of friction under ASTM D1894. For non-food industrial uses, the film must comply with REACH Annex XVII restrictions for heavy metals and with RoHS 2011/65/EU for electrical and electronic equipment packaging where applicable. When switching from a lower-density C4 LLDPE to LLDPE 3224, the first process adjustment is a melt temperature reduction of 5–8 °C to preserve bubble geometry and reduce edge weld instability. The converted articles include FFS sacks, construction liners, and heavy-gauge industrial bags.
Agricultural silage and greenhouse cover films use LLDPE 3224 less as a neat film former and more as a thermoplastic carrier for stabilizer packages. In a three-layer silage film, a typical layer distribution is 30 wt% outer UV-stabilized LLDPE 3224, 40 wt% core LLDPE 3224 blended with 10–20 wt% EVA, and 30 wt% inner cling layer of EVA-rich compound. The LLDPE layers normally contain 2.5–4.0 wt% UV masterbatch and 0.3–0.8 wt% hindered amine light stabilizer masterbatch. When mineral-filled infrared masterbatch is stored at relative humidity above 60 %, drying at 60–70 °C for 2 h is necessary to prevent foaming at the die. Greenhouse covers are produced at 150–200 µm thickness on blown film lines with a die gap of 1.8–2.4 mm, a blow-up ratio of 2.2:1–3.0:1, and a melt temperature of 195–210 °C. If the melt temperature exceeds 220 °C, certain benzophenone-type UV additives begin to volatilize, causing plate-out on the upper air ring lips and a detectable batch-to-batch drop in UV absorbance under ISO 4892-2 or ASTM G154. This is a production-scale failure mode when a line runs clear packaging film and heavily stabilized agricultural film on the same barrel profile without a separate purge protocol. Residual stabilizer in the die can elevate haze in subsequently produced clear film under ASTM D1003. Mechanical properties are tested under ISO 527-3, dart drop impact under ASTM D1709, and tear propagation under ASTM D1922. For agricultural covering films placed on the EU market, mechanical and installation performance is generally assessed against EN 13206; for silage films, EN 13207 may be referenced. There is no food-contact requirement in this segment, but the final film must comply with REACH Annex XVII and, where direct feed contact is specified, with EU 10/2011. Oxygen transmission rate of LLDPE measured under ASTM D3985 is generally two to three orders of magnitude higher than that of EVOH; therefore, in oxygen-sensitive silage applications, LLDPE 3224 is not used as the barrier layer but as the outer skin or core in coextruded structures that contain EVOH or polyamide.
LLDPE 3224 is used as the sealant web in five-layer and seven-layer flexible packaging structures where the outer web is BOPET or BOPP, the barrier layer is EVOH or polyamide, and the sealant layer must combine puncture resistance with stable heat-seal strength. The sealant layer typically occupies 20–35 % of the total web thickness; in an 80 µm blown coextrusion, the LLDPE 3224 skin is commonly 20–28 µm thick. The sealant-layer extruder is usually a 45–65 mm barrier screw with an L/D of 24:1–30:1, and the die temperature is held at 200–215 °C. Heat-seal strength is verified under ASTM F88/F88M, hot-tack under ASTM F1921, and gauge distribution under ISO 4593. Published data for this specific grade in production coextrusions is limited; therefore seal initiation must be determined experimentally at the intended sealant thickness, jaw pressure, and dwell time. In industrial practice, the presence of slip/antiblock masterbatch above 2.0 wt% raises the seal initiation temperature relative to the neat resin because the migrating erucamide or oleamide dilutes the seal surface; this shift is quantifiable by comparing ASTM F88 seal curves of neat and additivated film on the same line. The main process conflict is interlayer viscosity mismatch. If the sealant layer is run at a temperature lower than that of the adjacent tie resin, the higher viscosity of LLDPE 3224 relative to maleated tie resins can push the tie layer into the EVOH barrier layer, distorting the barrier and increasing oxygen transmission under ASTM D3985. A corrective action is to raise the sealant-layer extruder temperature by 5–10 °C while holding the barrier layer below 215 °C. The sealant web must comply with FDA 21 CFR 177.1520(c) and EU 10/2011, including an overall migration limit of 10 mg/dm² for food contact, plus REACH Annex XVII restrictions for additives and monomers. A production failure mode occurs when the sealant skin is run below 12 µm; gauge variation from the die can create localized seal leak channels at package corners, which appear as peel-strength outliers under ASTM F88. The converted articles include stand-up pouches, quad-seal bags, flow-wrap packages, and lidding films. When a coextrusion line is converted from metallocene-catalysed LLDPE to this grade, head pressure may change because of molecular architecture differences, and the layer distribution should be re-checked using in-line thickness sensing or off-line ISO 4593 rather than assuming unchanged screw speed.
Cast lamination and stretch-hood film production generally selects LLDPE resins with melt flow rates above 3.0 g/10 min, but LLDPE 3224 can be blended at 20–40 wt% into a cast film compound to raise puncture resistance and dilute gel counts when the main resin is a higher-MFR LLDPE or LDPE. The blend is extruded through a 1,800–2,400 mm flat die with a nominal die gap of 0.4–0.8 mm, an air gap of 100–180 mm, and a chill roll temperature of 20–30 °C. Melt temperature at the die is typically 230–245 °C because of the narrow die gap, but residence time should remain below 4 min to limit gel formation. At 20 wt% addition, the blend improves Elmendorf tear measured under ASTM D1922 and dart impact measured under ASTM D1709, without the draw resonance that can appear with pure 0.920 g/cm³ resin in high-draw cast film. Draw resonance is controlled by air gap length and melt temperature, not by raising melt flow index alone. The blend is used in adhesive-laminated lamination films, surface-protective base layers, and stretch-hood webs. Surface coefficient of friction is controlled with 0.5–1.5 wt% slip/antiblock masterbatch and tested under ASTM D1894; haze is measured under ASTM D1003 and increases if the chill roll temperature exceeds 35 °C or if the melt temperature exceeds 250 °C. On cast film lines, the operational boundary shifts from bubble stability to die-lip build-up; LLDPE 3224 processed at high shear can generate gel particles at die edges after 8–12 h continuous running, requiring scheduled lip cleaning and gel detection under ISO 18553. Food-contact cast film must satisfy FDA 21 CFR 177.1520(c) and EU 10/2011. The resulting web is often adhesive-laminated to BOPP or BOPET for flexible packaging.
Repelletizing of post-industrial film scrap uses LLDPE 3224 as a viscosity-modifying and gel-diluting feedstream in recycling extruders. In a two-stage recycling line with a 150 mm feeding screw, a melt filter screen changer of 120–150 mesh, and underwater pelletizing, the scrap may contain edge trim from blown or cast film containing LLDPE 3224, low-density polyethylene, and small amounts of slip or antiblock additive. The re-pelletizing operation adds 10–30 wt% virgin LLDPE 3224 to stripped and densified film flake to raise average melt viscosity and reduce the concentration of gels carried over from degraded material. Barrel temperatures are set at 160–200 °C, and the melt is filtered at 150–180 °C to avoid forward leakage from a worn screen changer. The main incompatibility is contamination with polypropylene, PET, or PVC; polypropylene flakes remain semi-solid at 180 °C and produce hard spots in the final pellets, while PVC degrades below 200 °C and releases hydrochloric acid, causing corrosion of die plates. Incoming scrap should be tested for density separation residue and for melt flow stability under ASTM D1238; pellet quality is assessed for gel count under ISO 18553. The final pellet is used as a blending component in refuse sacks, industrial liners, and construction films. No migration-sensitive compliance standard is applied if the resulting product is non-food; however, the recycled pellet must meet REACH Annex XVII restrictions for polycyclic aromatic hydrocarbons and heavy metals where the final film enters the EU market.
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Hanwha LLDPE 3224 is a linear low density polyethylene film resin based on butene comonomer chemistry and is specified for blown film and cast film conversion where a nominal density of 0.918 g/cm³ and a melt index of 2.0 g/10 min at 190 °C/2.16 kg provide controlled drawdown and mechanical integrity. The grade is produced with a Ziegler-Natta catalyst system, which yields a short-chain branching distribution that differs from high-pressure LDPE and from metallocene octene-based grades. In monolayer structures, the resin contributes higher tensile strength at break and greater puncture resistance than LDPE of comparable melt index; in coextruded structures, it functions as a sealant web or skin layer adjacent to barrier cores such as EVOH or nylon. The base polymer is not formulated with slip or antiblock additives unless specified on the purchase order. Because the density remains below 0.920 g/cm³, the product belongs to the LLDPE class rather than medium-density polyethylene and is not intended for rigid blow molding or pipe extrusion. Published data for specialized multilayer film properties are limited; each converter should confirm batch-specific values using the certificate of analysis.
Typical applications include agricultural film, lamination film, produce bags, and general-purpose consumer packaging. In agricultural films, the resin is often blended with LDPE and UV stabilizer masterbatches; greenhouse and tunnel films are evaluated for tensile elongation retention after xenon-arc exposure according to ISO 4892-2. In hygiene backsheet lamination, the resin is used as a sealing layer where low gel counts and uniform thickness control are required to prevent pinholes. Film thicknesses from 25 µm to 150 µm are common, with thicker agricultural films generally run at higher blow-up ratios. The butene comonomer provides puncture resistance and sealability but not premium clarity; haze values above 10% are acceptable in agricultural and industrial films but not in high-clarity display packaging.
Conventional LDPE produced in high-pressure tubular or autoclave reactors contains long-chain branching, which increases extensional viscosity and stabilizes the blown film bubble at high blow-up ratios. Hanwha LLDPE 3224 is a linear polymer without long-chain branching; its short-chain branches from butene comonomer reduce crystallinity and modulus but do not provide the same melt strength. At equivalent 2.0 g/10 min melt index, the LLDPE exhibits higher shear viscosity at low shear rates and lower shear thinning than LDPE. This shifts the process window: the LLDPE may require 3–5 °C higher die temperature or a slightly wider die gap to avoid melt fracture, but it permits more aggressive downgauging. Tensile strength at break and dart impact are higher than LDPE at 25–50 µm thickness because the linear chains and short-chain branches distribute stress more effectively under slow puncture. The trade-off appears in tear propagation and tear balance, where LDPE often displays higher machine-direction tear strength.
On a production-scale 90 mm grooved-feed single-screw blown film line with a 30:1 L/D barrier screw and a 250 mm spiral mandrel die, the resin typically generates head pressure between 28 MPa and 42 MPa at screw speeds from 60 min⁻¹ to 90 min⁻¹. Barrel temperature settings of 170 °C, 180 °C, 190 °C, and 205 °C from feed to metering, with adapter and die zones at 205–215 °C, maintain melt temperature in the 195–220 °C range. If the melt temperature falls below 188 °C, the film exhibits increased melt fracture, gauge bands, and pressure oscillations of ±1.5 MPa around the mean head pressure. If melt temperature exceeds 230 °C, oxidative chain scission may increase melt index and generate gel counts that become visible in films below 30 µm. Bubble stability is maintained at blow-up ratios between 1.8:1 and 2.5:1; a high-stalk configuration with a frost line height of 3–5 die diameters improves bubble symmetry. The processing window is therefore defined less by the polymer’s thermal stability than by melt strength and die-lip relaxation.
The following representative values are drawn from manufacturer technical literature for film resins of comparable density and melt index. Batch-specific certificate-of-analysis data govern; published data for this specific configuration is limited for certain specialty applications, and the values are not intended as sales specifications.
| Property | Test method | HANWHA LLDPE 3224 | Conventional LDPE | Metallocene hexene LLDPE |
|---|---|---|---|---|
| Density | ASTM D1505 | 0.918 ±0.002 g/cm³ | 0.924 ±0.002 g/cm³ | 0.918 ±0.002 g/cm³ |
| Melt index | ASTM D1238 | 2.0 g/10 min | 2.0 g/10 min | 1.0 g/10 min |
| Dart drop impact | ASTM D1709 Method A | 90–140 g | 70–95 g | 300–400 g |
| Elmendorf tear, MD | ASTM D1922 | 250–350 g | 180–240 g | 400–600 g |
| Tensile strength at break, MD | ASTM D882 | 35–45 MPa | 22–28 MPa | 45–55 MPa |
| Elongation at break, MD | ASTM D882 | 700–800% | 400–500% | 600–700% |
| Haze | ASTM D1003 | 8–12% | 6–8% | 4–7% |
| Gloss at 45° | ASTM D2457 | 60–70 | 65–75 | 70–80 |
| Seal initiation temperature | ASTM F88 | 98–104 °C | 104–110 °C | 94–100 °C |
The comparative matrix illustrates the principal technical difference: metallocene hexene LLDPE offers higher dart impact and lower seal initiation temperature but generates higher extruder torque and is more sensitive to melt fracture on narrow-die-gap lines. Conventional LDPE has superior optical properties and bubble stability but lower tensile strength at break and lower dart impact. HANWHA LLDPE 3224 occupies an intermediate position in dart impact and optics, with processing behavior closer to conventional Ziegler-Natta LLDPE but with a higher melt index than many general-purpose film grades. Blends of 10–30 wt% LDPE are used in collation shrink and agricultural films to increase bubble stability and modify tear balance; blends of 5–15 wt% metallocene LLDPE are used to improve dart impact without sacrificing seal performance.
In agricultural films, weathering resistance is measured by elongation retention after xenon-arc exposure according to ISO 4892-2; the resin itself contains no UV stabilizer, so additive masterbatch choice controls service life. In hygiene and medical packaging, the resin may be coextruded with HDPE or metallocene LLDPE layers; absence of high gel counts is critical because gels create pinholes in 12–20 µm cast film. The butene comonomer improves puncture resistance and sealability but not optical clarity; haze values above 10% may be acceptable in agricultural films but not in premium display packaging.
Capillary rheometry at 190 °C indicates shear viscosity decreasing from approximately 1,200 Pa·s at 100 s⁻¹ to 200 Pa·s at 1,000 s⁻¹ for this class of butene LLDPE; the power-law index is approximately 0.35–0.45. These values are approximate, and published data for this specific configuration is limited; rheological behavior should be measured on the actual lot using a capillary rheometer according to ASTM D3835. The viscosity curve explains why the resin flows adequately in film dies but can overheat in high-shear extruder zones if screw speed is raised without corresponding barrel-temperature adjustment.
Film structures that include HANWHA LLDPE 3224 as the sealant web operate under stricter heat-seal and adhesion boundaries than single-layer stretch wrap. The seal initiation temperature of the resin is close to 100 °C, but robust seal strength typically requires jaw temperatures of 115–135 °C, pressures of 0.5–1.5 N/mm², and dwell times of 0.5–1.0 s. Below those temperatures, cold seals may fail at loads below 2.0 N/15 mm; above them, burn-through and seal thinning appear in films thinner than 30 µm. Hot-tack performance is controlled by crystallization rate and is lower than metallocene grades but higher than LDPE at equivalent thickness. For lamination, the film surface should be corona treated to 38–42 dyn/cm immediately before coating or extrusion lamination; treatment decay below 36 dyn/cm reduces adhesion to solvent-based adhesives and water-based inks. In multilayer barrier structures, insufficient tie-layer adhesion or excessive slip additive migration to the surface can generate delamination at the seal/barrier interface. The resin does not contain a built-in adhesion promoter and is not designed for direct extrusion lamination to aluminum foil without a tie layer.
Food-contact applications using HANWHA LLDPE 3224 require the converter to evaluate the final food-contact article rather than the resin in isolation. The base olefin polymer may fall within FDA 21 CFR 177.1520(c) when used in accordance with the conditions of the regulation, but the presence of additives, colorants, and processing aids may require separate clearances. In the European Union, EU Regulation No 10/2011 requires that finished articles meet an overall migration limit of 10 mg/dm² in food simulants; the migration result depends on film thickness, time, temperature, and simulant class. The resin is not marketed as a medical-grade polymer, and published biocompatibility data according to ISO 10993 are limited. Processors must not infer that compliance with a resin positive list alone demonstrates compliance of the fabricated article.
| Regulatory reference | Scope | Converter obligation |
|---|---|---|
| FDA 21 CFR 177.1520(c) | Olefin polymers for food-contact use | Confirm polymer density, thickness, and end-use conditions; migration testing if not exempt |
| EU Regulation No 10/2011, Annex I and II | Plastic materials and articles intended for food contact | Document overall migration ≤ 10 mg/dm² and specific migration limits for additives |
| REACH Regulation 1907/2006 | Registration, evaluation, authorisation, and restriction of chemicals | Verify SVHC content below 0.1 wt% and communicate safe use information |
| RoHS Directive 2011/65/EU | Restriction of hazardous substances in electrical and electronic equipment | Confirm lead, mercury, cadmium, hexavalent chromium, PBB, and PBDE do not exceed maximum concentration values |
Storage conditions follow standard olefin practice: keep the resin at 5–40 °C and below 60% RH in sealed containers. If cold resin is moved into a warm humid production hall, surface condensation can introduce moisture into the feed throat; drying at 60–70 °C for 2–4 h in a desiccant or hot-air drier removes surface water. The melt should not be combined with strong oxidizing agents or with peroxide masterbatches above 0.1 wt% unless intentional vis-breaking is specified, because excessive peroxide reduces molecular weight, lowers dart impact, and shifts the melt index upward. Acidic species and decomposing phenolic antioxidants at process temperatures above 230 °C can promote gel formation; residence time above that temperature should be minimized. The operational envelope therefore includes melt temperature below 225 °C, head pressure monitoring, and seal strength verification against ASTM F88.