| HS Code | 994450 |
| Productname | Braskem LH118 Blown Film Extrusion Linear Low Density Polyethylene |
| Manufacturer | Braskem |
| Grade | LH118 |
| Polymertype | Linear Low Density Polyethylene (LLDPE) |
| Processingmethod | Blown Film Extrusion |
| Form | Pellets |
| Density | 0.918 g/cm³ |
| Meltindex | 0.85 g/10 min (190°C/2.16 kg) |
| Meltingpoint | 121 °C |
| Vicatsofteningpoint | 94 °C |
| Tensilestrengthatyield | 10 MPa |
| Tensilestrengthatbreak | 30 MPa |
| Elongationatbreak | 700 % |
| Dartdropimpact | 200 g |
| Elmendorftear | 300 g |
| Haze | 12 % |
| Gloss | 50 (45°) |
| Coefficientoffriction | 0.2 |
As an accredited Braskem LH118 Blown Film Extrusion Linear Low Density Polyethylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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In blown film lines operating at die gaps exceeding 2.0 mm, the formulation constraints imposed by silage and forage wrap extrusion diverge sharply from those governing conventional packaging films. Agricultural stretch film produced from butene-comonomer LLDPE demands simultaneous optimization of two mutually antagonistic performance axes: self-adhesion (cling) and long-term UV weathering resistance. The cling requirement necessitates incorporation of polyisobutylene (PIB) or specialty amorphous polyalphaolefin (APAO) tackifiers at 1.0–3.0 wt% into the core or skin layers of a coextruded structure; however, these low-molecular-weight components exhibit shear-induced migration during blown film extrusion, accumulating at the die lip and initiating die-lip buildup within 8–12 h of continuous operation on lines equipped with 90–150 mm diameter dies and L/D 24:1–30:1 extruders. The UV stabilization package—typically hindered amine light stabilizers (HALS) at 0.3–0.8 wt% combined with a benzotriazole or benzophenone UV absorber at 0.1–0.3 wt%—further complicates extrusion stability because HALS compounds with amine functionality can interact with the tackifier phase, reducing tackifier mobility and lowering the cling force measured as the 180° peel adhesion per ISO 11339. A three-layer A-B-A coextrusion configuration, with LLDPE skins and a LDPE-rich core at a blend ratio of 70/30 to 85/15 (LLDPE/LDPE), addresses this conflict by confining the tackifier to the core layer, where migration to the die lip is kinetically restricted by the encapsulation of the skin layers. Industry compliance for silage stretch film is governed by EN 13206, which specifies minimum elongation at break values per ISO 527-3 (typically ≥250% in both machine and transverse directions for silage wrap) and puncture resistance testing per EN 14477; additionally, European production requires full REACH registration and Annex XVII restriction screening of tackifier and stabilizer constituents. The blown film process for silage wrap uses blow-up ratios (BUR) of 2.5:1 to 3.5:1, internal bubble cooling (IBC) for gauge uniformity, and frost line heights maintained at 6–10 times the die diameter to balance machine-direction and transverse-direction tensile properties; failure to hold frost line height within ±10% of the target produces gauge bands and localized cling variability that render film rejects at the bale-wrapping stage. Terminal product types include round bale wrap at 25 µm nominal thickness, square bale wrap at 30–35 µm, silage pit cover sheeting at 100–150 µm, and forage stretch wrap for combination balers, each requiring distinct cling force targets measured per ISO 11339 and elongation recovery properties assessed by ISO 527-3 hysteresis testing.
The primary process conflict in freezer-grade film production arises from the interplay between slip agent migration kinetics and heat seal polymer interdiffusion at the seal interface. Butene-comonomer LLDPE with a density of 0.918 g/cm³ and melt flow rate of 1.0 g/10 min (ISO 1133-1:2022, 190 °C/2.16 kg) exhibits a seal initiation temperature (SIT) typically in the 92–105 °C range when measured by ASTM F1921 Method A on vertical form-fill-seal (VFFS) equipment. Frozen food packaging requires the simultaneous achievement of a coefficient of friction (COF) below 0.20 per ASTM D1894 to permit reliable bag opening and automated pouch handling, and a hot tack strength above 2.5 N/25 mm per ASTM F1921 to prevent seal creep and product blowout during vertical fill operations at line speeds of 40–80 packages per minute. Erucamide slip agent, incorporated at 500–1200 ppm, migrates to the film surface within 24–72 h of extrusion, reducing the kinetic COF from 0.45–0.55 to 0.12–0.18; yet this same surface bloom creates a low-surface-energy monolayer that physically impedes polymer chain interdiffusion at the seal interface, elevating the measured seal initiation temperature by 3–8 °C and reducing the hot tack plateau. Synthetic silica antiblock (surface area 200–400 m²/g, median particle size 3–6 µm) at 2000–5000 ppm compounds the optical penalty: film haze measured per ASTM D1003 increases from 6–8% for unstabilized LLDPE to 12–18% when antiblock loadings approach 5000 ppm, and gloss at 60° per ASTM D2457 drops from 70–80 GU to 40–50 GU. Production-scale VFFS lines equipped with jaw-type sealers and 5–10 mm wide seal bars operating at 120–145 °C sealing temperature and 0.3–0.6 s dwell time are particularly sensitive to the shift in SIT induced by slip agent levels exceeding 1000 ppm; field data from frozen vegetable packaging lines document intermittent seal failures characterized by channel leakers at the gusset fold when erucamide loading exceeds 1200 ppm in monolayer films. The formulation resolution for this conflict involves either reducing slip agent to 500–800 ppm and compensating with external lubrication on the bagger, or adopting a two-layer coextruded structure in which the sealant layer contains zero slip agent (0 ppm erucamide) and the outer layer carries the full slip package, thereby preserving seal integrity while maintaining the required surface friction characteristics. FDA 21 CFR 177.1520(c) paragraphs 3.1a and 3.2a govern food contact compliance for LLDPE in this application, with extraction testing per FDA guidance requiring maximum extractable fraction below 5.5 wt% in n-hexane and below 2.5 wt% in xylene; EU Regulation 10/2011 as amended imposes an overall migration limit of 10 mg/dm² when tested in food simulant D2 (vegetable oil) or substitute simulants per Commission Regulation (EU) 2020/1245. Downstream processing on blown film lines uses die gaps of 1.8–2.4 mm—narrower than those used for agricultural film to preserve optical properties—with BUR of 2.0:1 to 2.6:1, melt temperatures held at 195–210 °C to minimize gel formation from slip agent thermal degradation, and IBC or external air ring cooling configured for a 1% or better gauge variation across the web. Terminal product types include individually quick frozen (IQF) vegetable bags at 50–75 µm, frozen fruit pouches, ice cream pillow packs, frozen bakery product wrap, and frozen meat barrier films in coextrusion with polyamide or EVOH barrier layers.
| Erucamide Slip Loading (ppm) | Synthetic Silica Antiblock (ppm) | Seal Initiation Temperature (°C) | Hot Tack at 120°C (N/25 mm) | Kinetic COF After 72 h Aging | Haze ASTM D1003 (%) |
|---|---|---|---|---|---|
| 500 | 2000 | 94 | 4.5 | 0.28 | 8 |
| 750 | 3000 | 97 | 3.9 | 0.19 | 10 |
| 1000 | 4000 | 101 | 3.2 | 0.14 | 13 |
| 1500 | 5000 | 107 | 2.3 | 0.11 | 17 |
Tubular film production for flexible intermediate bulk container (FIBC) liners demands a different balance of dart impact resistance and flexural modulus than any other downstream application of butene-comonomer LLDPE. FIBC liners are extruded at thicknesses of 80–150 µm, where the blown film process must maintain bubble stability while operating at BURs as low as 1.5:1 to 2.0:1—significantly lower than the 2.5:1 to 3.5:1 range typical of packaging films—because low blow-up ratios preserve the machine-direction tear resistance that FIBC liner certification testing requires. The formulation for this application is 100% LLDPE with a melt index of 0.8–1.0 g/10 min, optionally compounded with 20–40 wt% metallocene-catalyzed LLDPE (mLLDPE) of similar density (0.918 g/cm³) to elevate dart impact strength measured per ASTM D1709 Method A from approximately 400 g (unmodified butene-LLDPE at 100 µm) to 600–800 g without sacrificing the low-temperature flex-crack resistance required for liner deployment at sub-zero ambient conditions. The blown film process for FIBC liners is constrained by the requirement for extremely low gel content and homogeneous additive dispersion across the web; lines configured with L/D 30:1 extruders, barrier screws with Maddock mixing sections, and screen changers with 100–150 mesh screens are standard. Industry compliance is governed by the UN Recommendations on the Transport of Dangerous Goods, under which FIBCs for hazardous materials require type certification as UN 13H2 (flexible IBC, coated/woven plastic, with liner) or 13H3 (woven plastic with liner), and liner material must demonstrate compatibility with the packaged substance per UN 4.1.1.4 test provisions; food-grade FIBC liners additionally require FDA 21 CFR 177.1520 compliance for olefin polymer food contact surfaces and ISO 21898 as the specification standard for FIBCs used with non-hazardous materials. Downstream processes convert the blown film tube into inserted liners, form-fitted liners, or pre-made bag liners through heat sealing, gusset insertion, and fitting attachment operations; terminal product types include drum liners at 100–125 µm, FIBC insert liners at 80–120 µm, container liners for 20 ft and 40 ft ISO containers at 150–200 µm, and shipping sack inner plies.
Collation shrink film lines configured with double-bubble orientation equipment require precise control of molecular orientation during the secondary bubble inflation stage, where the extruded primary tube is reheated to a temperature within 10–20 °C of the crystalline melting point and inflated to induce biaxial orientation. The addition of LLDPE to LDPE in collation shrink blends modifies the orientation temperature window, the shrink force, and the puncture resistance of the final film. At LLDPE loadings below 30 wt%, the shrink tension measured per ISO 14616 remains dominated by the branched LDPE architecture, which provides high machine-direction shrink force but low transverse-direction shrink uniformity; at LLDPE loadings between 30 wt% and 40 wt%, the linear architecture of the butene-LLDPE contributes to improved transverse-direction orientation and raises dart impact resistance measured per ASTM D1709 Method A by 40–70% relative to 100% LDPE control films of equivalent gauge, but the shrink force begins to plateau and subsequently declines as the linear chains resist the secondary bubble extension. The formulation for collation shrink film is therefore a compromise: commercial blends range from 20/80 to 50/50 LLDPE/LDPE, with the 30/70 to 40/60 range representing the practical upper limit for applications requiring minimum 15% free shrink in both machine and transverse directions when measured per ASTM D2732 in a 135 °C oil bath for 15 s. Slip agents are intentionally omitted or reduced to 200–400 ppm of erucamide in collation shrink film because the coefficient of friction on the outer surface must remain above 0.30 per ASTM D1894 to maintain pallet load stability during handling, and the absence of slip contributes to the scratch sensitivity that must be managed in converting operations. Compliance for collation shrink film falls under EU Regulation 10/2011 for food contact applications and ASTM D2732 as the standard test method for unrestrained linear thermal shrinkage. Downstream production on double-bubble lines involves the use of a primary extruder with L/D 24:1–28:1, a heating section with infrared or hot-air ovens calibrated to achieve a bubble temperature of 110–125 °C prior to secondary inflation, and collapsing frames configured for shaft or surface winding; the secondary BUR is set at 2.5:1 to 3.5:1 to achieve balanced free shrink values, and the line speed is constrained to 60–120 m/min because higher draw rates induce bubble instabilities that create gauge bands and shrink anisotropy. Terminal product types include beverage multipack collation at 45–60 µm, can bundling films at 50–70 µm, PET bottle collation shrink at 50–65 µm, and combined package shrink wrap for pharmaceutical and personal care product trays.
Sub-slab vapor barrier sheeting represents the least formulationally complex downstream application for butene-LLDPE, requiring a 100% LLDPE formulation with carbon black masterbatch at 2.0–3.0 wt% for UV resistance per ASTM D4397 and no slip or antiblock additives. The production process on wide-width blown film lines using L/D 30:1 extruders with IBC operates at BURs of 2.0:1 to 2.5:1 and produces sheeting at 0.25–0.50 mm (10–20 mil) that must achieve water vapor permeance below 0.006 perms (0.34 ng/(Pa·s·m²)) when tested per ASTM F1249 at 23 °C and 50% RH. Compliance is verified against ASTM E1745 Classes A, B, and C, which establish minimum thickness, tensile strength, puncture resistance, and permeance requirements, and installation is governed by ACI 302.1R guidance for concrete floor slabs. Terminal product types include under-slab vapor retarders, crawl space ground liners, and foundation wall vapor barriers.
Five-layer and three-layer coextrusion lines producing bag-in-box liners assign LLDPE to the sealant layers, where low seal initiation temperature and flex-crack resistance determine product qualification for liquid packaging. The sealant layer formulation is typically 100% butene-LLDPE with no slip agent in the sealant layer to avoid inhibition of heat seal strength, while the outer layer carries 500–1000 ppm erucamide for machine handling; the LLDPE sealant layers constitute 30–45% of the total film thickness in a three-layer structure of LLDPE/tie/nylon/EVOH/tie/LLDPE or LLDPE/tie/EVOH/tie/LLDPE. Flex-crack resistance is measured per ASTM F392 using the Gelbo flex test, and the failure criterion—requiring no leakage through pinholes after 10,000 flex cycles for wine bag-in-box liners—dictates the use of LLDPE with superior low-temperature ductility rather than LDPE in the sealant layer. Compliance is governed by FDA 21 CFR 177.1520 for the olefin polymer layers and EU Regulation 10/2011 with specific migration limits for barrier layer constituents, and the overall migration limit of 10 mg/dm² must be demonstrated in food simulant D2 or substitute n-heptane per the applicable standard. The production process on coextrusion blown film lines with up to five extruders requires die gaps of 1.8–2.2 mm, BUR of 1.8:1 to 2.2:1, and melt temperatures of 195–215 °C for the LLDPE layers; gauge uniformity of ±2% or better across the web is essential because flex-crack initiation is preferentially localized in thin-gauge regions. Terminal product types include wine bag-in-box liners at 70–100 µm, dairy product bag liners, sauce dispenser pouches, and industrial liquid liners for ink, adhesive, and chemical intermediate packaging.
| Application | Primary Specification Standard | Key Test Method | Regulatory Framework |
|---|---|---|---|
| Silage and forage stretch film | EN 13206 | ISO 527-3; ISO 11339; EN 14477 | REACH Annex XVII |
| Frozen food packaging | FDA 21 CFR 177.1520(c) 3.1a/3.2a | ASTM F1921; ASTM D1894; ASTM D1003 | EU 10/2011; EC 1935/2004 |
| FIBC and container liners | ISO 21898; UN 13H2/13H3 | ASTM D1709; ASTM F392 | UN Recommendations on Transport of Dangerous Goods |
| Collation shrink film | ASTM D2732 | ISO 14616; ASTM D1709 | EU 10/2011 |
| Sub-slab vapor barrier | ASTM E1745 | ASTM F1249; ASTM D4397 | ACI 302.1R; IBC 2018 Section 1907 |
| Bag-in-box liner | FDA 21 CFR 177.1520 | ASTM F392; ASTM F1921 | EU 10/2011; EC 1935/2004 |
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