Products

Lotte Chemical LLDPE Titanvene LL0335AA

    • Product Name: Lotte Chemical LLDPE Titanvene LL0335AA
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications
    HS Code 429047
    Density 0.933 g/cm³
    Melt Flow Rate 190c 2 16kg 0.35 g/10min
    Melting Point 126 °C
    Vicat Softening Point 105 °C
    Tensile Strength Yield Md 16 MPa
    Tensile Strength Yield Td 14 MPa
    Tensile Strength Break Md 26 MPa
    Tensile Strength Break Td 20 MPa
    Elongation At Break Md 550 %
    Elongation At Break Td 700 %
    Dart Impact Strength 110 g
    Haze 12 %
    Gloss 60 Degrees 70

    As an accredited Lotte Chemical LLDPE Titanvene LL0335AA factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Lotte Chemical LLDPE Titanvene LL0335AA is packaged in 25 kg polyethylene bags, palletized and stretch-wrapped for safe transport and storage.
    Container Loading (20′ FCL) 20′ FCL container loading of Lotte Chemical LLDPE Titanvene LL0335AA, ensuring safe, efficient transport and optimal space utilization.
    Shipping Lotte Chemical LLDPE Titanvene LL0335AA is a linear low-density polyethylene resin, supplied as free-flowing pellets. Ship in clean, dry containers or railcars, protected from moisture and direct sunlight. Avoid elevated temperatures and sharp impacts. Ensure proper ventilation and secure loading to prevent contamination, shifting, or damage during transit.
    Storage Store Lotte Chemical LLDPE Titanvene LL0335AA in a dry, clean, well-ventilated area away from direct sunlight, heat, and ignition sources. Keep bags sealed or in closed containers to prevent moisture and contamination. Avoid contact with strong oxidizers. Maintain moderate temperatures and proper inventory rotation to preserve resin quality.
    Shelf Life Shelf life is indefinite when stored in original packaging, away from direct sunlight, heat, and moisture.
    Application of Lotte Chemical LLDPE Titanvene LL0335AA

    LL0335AA is a butene-comonomer linear low-density polyethylene with a nominal melt flow rate of 3.5 g/10 min when tested under ISO 1133-1:2022 at 190°C/2.16 kg and a nominal density of 0.918 g/cm³ when tested under ISO 1183-1:2019. The resin is supplied as a pelletised film-grade raw material and is not recommended for applications requiring high melt strength such as blow moulding of large containers or deep-draw thermoforming. Downstream application segments shown here are restricted to converting routes where the rheological profile is compatible with blown film, cast film, extrusion lamination, and compounding operations. Unless otherwise indicated, the stated addition ratios are weight percentages of the total polymer phase and exclude external liquid additives introduced at the feed throat or slip dosing unit.

    On a 75 mm grooved-feed blown film line running LL0335AA at melt temperature 190–205°C, the polymer matrix for frozen food packaging is set at 60–75 wt% LL0335AA, 10–20 wt% LDPE, 5–10 wt% white masterbatch, and 1–2 wt% slip/antiblock masterbatch. The LDPE fraction is not a diluent; it supplies the melt strength required when the blow-up ratio is moved from 2.5:1 to 3.5:1 on a die gap of 1.8–2.3 mm. Frost line height is maintained at 3–5 die diameters, and internal bubble cooling is used only above 4.0:1 blow-up ratio because the 3.5 g/10 min melt flow rate lowers bubble stability under high-stalk geometry. Surface treatment is set at 38–42 mN/m for subsequent flexographic printing. Compliance is anchored to FDA 21 CFR 177.1520(c) 3.2a, EU Regulation 10/2011 Annex I, and China GB 4806.7-2016; converters must re-run overall migration tests on the final film because the slip/antiblock package alters the migration profile. Terminal product types are frozen vegetable pouches, seafood bags, ice bags, and thin-gauge carrier bags. Dart impact is measured under ASTM D1709-16a; tear propagation under ISO 6383-2:1983. The primary failure mode observed on production lines is bubble flutter at blow-up ratios above 4.0:1, which appears as gauge bands at the collapsing frame and is corrected by reducing draw speed rather than increasing melt temperature above 210°C, where gel specks begin to form.

    What Limits Melt Curtain Stability in Extrusion Lamination at 305°C?

    Extrusion lamination with LL0335AA onto aluminium foil, PET, BOPP, or paper is run at melt temperature 290–320°C, where adhesion to unprimed substrates depends on oxidative degradation of the polymer surface in the air gap. Melt curtain stability is limited by the draw ratio between the die and the chill roll: an air gap of 150–250 mm with a slot die opening of 0.5–0.8 mm and line speed above 100 m/min will draw the film to 12–25 µm, and exceeding that draw ratio can initiate edge neck-in and draw resonance. The polymer phase for lamination is 60–80 wt% LL0335AA and 20–40 wt% LDPE; the LDPE raises melt strength but if the LDPE content exceeds 40 wt% the seal initiation temperature moves upward and the interlayer adhesion to BOPP is reduced. For aluminium foil structures requiring T-peel adhesion under ASTM D1876-08, a maleic anhydride-modified tie resin is dosed at 2–5 wt% in the melt stream before the die. The extrusion line typically uses a 90–150 mm single-screw extruder with L/D 30:1, a barrier screw, and a deckled flat die. Ozone treatment at the melt curtain is applied within the range of 0.3–0.6 mg/L, measured at the die exit, to raise surface oxidation and adhesion without breaching FDA 21 CFR 177.1520(c) 3.2a, EU Regulation 10/2011 Annex I, and Regulation (EC) No 2023/2006 Good Manufacturing Practice. Terminal products are snack wrapping laminates, single-serve sachet webs, pet food pouches, and sealant layers for aseptic cartons. A production-scale conflict arises at low line speed: below 100 m/min, the longer residence time in the air gap oxidises the melt curtain excessively, creating odour and brown specks; the melt temperature should then be reduced to the lower end of the window, but that simultaneously lowers foil peel strength. This boundary is monitored by film odour panels and T-peel measurements on the start-up roll.

    When LL0335AA is coextruded as the core of a three-layer cast film for surface protection applications, the polymer phase is formulated at 65–80 wt% LL0335AA in the core, 20–35 wt% LDPE in the skins, and 5–15 wt% EVA or POE in the cling skin for temporary adhesion. The slot die gap is held at 0.5–0.8 mm; the melt curtain is quenched on a matte or polished chill roll at 18–28°C, and a vacuum box and air knife stabilise the sheet before the wound roll. Line speeds of 200–400 m/min are typical on a 75–150 mm single-screw extruder with L/D 30:1. Corona treatment at 42–48 mN/m is applied after slitting to improve anchorage of post-applied inks or labels; wetting tension is verified under ISO 8296:2003. Compliance for industrial protective film is anchored to RoHS Directive 2011/65/EU Annex II, REACH Regulation (EC) No 1907/2006, and CONEG heavy metal limits, rather than food-contact regulations, because the final product is used as a temporary shield. Terminal product types include protective films for stainless steel sheet, painted metal panels, PVC window profiles, and acrylic or polycarbonate sheet. Peel adhesion is measured under ASTM D3330-04; adhesion above 200 g/25 mm is avoided on freshly painted surfaces where cohesive film failure is not allowed. A known processing boundary is chill roll plate-out from low-molecular-weight oligomers when melt temperature exceeds 240°C; the deposits appear as waxy particles on the roll surface and transfer to the film as surface haze, requiring line stoppage every 48–72 hours unless roll cleaning is automated.

    Masterbatch Carrier Resin Performance and Melt Filtration Pressure Drop

    Compounding LL0335AA as a carrier resin in masterbatch production uses the 3.5 g/10 min melt flow rate to wet pigment surfaces and reduce heat generation during dispersion, but it also lowers pressure generation relative to a 0.8–2.0 g/10 min LDPE carrier. The formulation window is 30–55 wt% LL0335AA carrier, 40–60 wt% pigment or filler, and 2–8 wt% dispersing aid; colour masterbatches are subsequently let down at 2–5 wt% into PE blown film or injection moulding. A co-rotating twin-screw extruder of 40–75 mm diameter and L/D 40:1–48:1 is operated at screw speed 400–700 rpm with melt temperature 190–230°C. Melt filtration through a 150–250 µm screen pack is standard before pelletising; pressure drop across the screen pack is monitored against the breaker plate rating, and a rapid pressure increase indicates pigment agglomerate plugging rather than carrier degradation. Underwater pelletising is used in most plants; the melt inlet temperature must remain above 185°C to avoid strand breakage at the water bath. Compliance is established under RoHS Directive 2011/65/EU Annex II, REACH SVHC screening, and ISO 11469:2016 for resin marking. Terminal product classes are colour masterbatch, white masterbatch, and additive masterbatch for PE film and moulding. The incompatibility boundary is strong oxidising pigments or fillers that catalyse polyolefin chain scission in the carrier; formulation development must include capillary rheometry under ISO 11443 to verify melt stability over a 20-minute residence test.

    If Tubular Film Bubble Geometry Is Fixed by High-Stalk Cooling for Heavy-Duty Sack Applications

    In heavy-duty sack film, LL0335AA is used as an impact modifier for HDPE film grades rather than as the main stiffness resin. The blend is set at 15–30 wt% LL0335AA with 70–85 wt% HDPE and 0.5–1 wt% polymer processing aid; this raises dart impact and Elmendorf tear propagation while maintaining the secant modulus required for sack opening and stacking. On a high-stalk tubular film line, the die gap is held at 2.0–2.8 mm, blow-up ratio is 3:1–5:1, and film thickness is 50–120 µm. Melt temperature is kept at 190–210°C; internal bubble cooling is used to set frost line height at 4–8 die diameters. The neck height and stalk cooling intensity determine orientation balance under ISO 527-3:2018 tensile testing; a one-sided shift in bubble temperature is a common source of gauge variation at the collapsing frame. Compliance standards for the segment are ISO 21898:2004 for packaging sacks, ASTM D1709-16a for dart impact, ISO 527-3:2018 for tensile properties, and REACH for polymer and additive registration. Terminal product types include cement sacks, fertilizer sacks, polymer resin packaging, and animal feed sacks. The limiting formulation boundary is at 40 wt% LL0335AA: above this level, the blend loses bending stiffness and shows increased elongation under stacked load. Published data for this specific blend ratio in high-stalk heavy-duty sack technology is limited; converters should conduct their own 30-day stacking trials instead of extrapolating from general-purpose blown film data.

    Addition of 20–30 wt% metallocene LLDPE to LL0335AA modifies the seal initiation temperature in high-speed vertical form-fill-seal films because butene LLDPE alone has lower hot-tack strength than metallocene grades at the same film thickness. The sealant layer uses 55–75 wt% LL0335AA, 20–30 wt% mLLDPE, 5–15 wt% LDPE, and 1–3 wt% slip/antiblock masterbatch. The film is blown on a die gap of 1.6–2.2 mm at a blow-up ratio of 2.0:1–3.0:1, then converted on VFFS machines with sealing jaw temperatures of 115–140°C and dwell times of 0.2–0.5 s. Hot tack is characterised under ASTM F1921-12; seal strength under ASTM F88/F88M-15. Compliance for food contact follows FDA 21 CFR 177.1520(c) 3.2a and EU Regulation 10/2011 Annex I; converters must revalidate migration after the addition of mLLDPE and slip/antiblock additives because each additive shifts the overall migration profile. Terminal product types include sugar and salt sachets, soup powder sachets, dried food pouches, and non-sterile disposable packaging. A critical boundary is high-speed horizontal form-fill-seal operation above 120 cycles/min: published data for this exact LL0335AA/mLLDPE blend on HFFS is limited, and the lower melt strength of LL0335AA can cause film deformation at seal jaw temperatures above 140°C. Processors running HFFS evaluate package integrity with ASTM F1921-12 hot-tack and ASTM F88/F88M-15 seal strength before committing to line speeds above the published data envelope.

    Free Quote

    Competitive Lotte Chemical LLDPE Titanvene LL0335AA prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: admin@ascent-chem.com

    Inquiry

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Lotte Chemical LLDPE Titanvene LL0335AA is a butene-comonomer linear low density polyethylene supplied for blown film conversion. The standard resin specification is anchored by two values: nominal density of 0.920 g/cm³ measured by ISO 1183-1 and melt mass-flow rate of 0.35 g/10 min measured at 190 °C under 2.16 kg load in accordance with ISO 1133-1. These values place the grade in the low-melt-flow-rate segment of linear film polyethylene. The butene comonomer introduces short-chain branching that disrupts crystallite packing, lowers stiffness relative to medium-density polyethylene, and raises impact and tear capacity relative to high-pressure low density polyethylene at equivalent gauge. The product is not a metallocene-catalysed resin; its broader molecular architecture produces a distinctly different rheological response from single-site LLDPE film grades.

    Rheological and Density Specification Boundaries

    The melt mass-flow rate of 0.35 g/10 min functions as the primary resin-lot control because it governs melt viscosity and extruder motor load. On a 75 mm single-screw extruder with 24:1 L/D and a 200 mm spiral-mandrel die, conversion from a 0.9 g/10 min LLDPE grade to Titanvene LL0335AA can raise screw motor load; plant observations on such lines indicate that operators commonly compensate by increasing barrel zone settings by 5 °C to 10 °C and reducing screw speed until the die head pressure stabilises. Detailed gel permeation chromatographic molecular weight distribution and comonomer branch frequency are not routinely published for this configuration; therefore, exact melt-strength predictions require rheological measurement on the intended extrusion line rather than extrapolation from MFR alone. Density at 0.920 g/cm³ reflects a low crystalline fraction, but differential scanning calorimetry data are not consistently supplied on standard certificates of analysis.

    What Changes When the Resin Is Run on a High-Stalk Blown Film Line?

    In high-stalk film extrusion, bubble stability is controlled by die gap, blow-up ratio, frost-line height, and melt relaxation. The low melt flow rate of LL0335AA supports a longer melt relaxation time relative to higher-MFR LLDPE, which assists stalk stability at elevated frost-line positions. Starting conditions for film from 40 μm to 80 μm typically include a die gap of 1.6 mm to 2.4 mm, blow-up ratio of 2.0:1 to 3.0:1, and frost-line height of 6 to 10 die diameters. High-stalk operation preferentially orients the film in the machine direction; if the frost line is set too low, retained orientation can increase machine-direction shrink. Cooling air temperature, internal bubble cooling load, and air-ring geometry shift the frost-line position and should be adjusted to stabilise the bubble before any change in take-off speed.

    Mechanical property evaluation of Titanvene LL0335AA must be performed on finished blown film rather than on pellets. Dart impact by ASTM D1709/D1709M, Elmendorf tear by ASTM D1922 or ISO 6383-2, and tensile properties by ASTM D882 are the standard conversion-level methods. The machine-direction to transverse-direction property balance responds strongly to die gap and stalk height: narrow die gaps can raise machine-direction tear, while higher transverse blow-up ratios can increase transverse-direction tear. Published film property values are often generated on laboratory blown film lines and should not be used as manufacturing release limits without commercial-line validation.

    When LL0335AA Replaces High-Pressure LDPE in Heavy-Duty Sack Applications

    Replacement of high-pressure LDPE with Titanvene LL0335AA in thick-film sacks shifts the property profile toward higher puncture resistance and higher elongation at break, but reduces melt strength at comparable melt temperature. High-pressure LDPE contains long-chain branching that produces strain hardening and high melt tension; the linear butene-copolymer structure of LL0335AA lacks this long-chain branch population. In heavy-duty sack lines, that difference may require a reduction in stalk height or an increase in melt temperature to prevent bubble instability. The economic offset is downgauging: a 100 μm LLDPE film can often replace a 120 μm LDPE film in puncture-intensive service because the LLDPE resin has higher tensile resistance per unit thickness. This substitution must be verified by end-user stacking and drop testing; no single tensile value is sufficient.

    Against other LLDPE film grades, the main distinction is comonomer type. Butene-based LL0335AA is produced with shorter branch lengths than hexene-based LLDPE; at an equal density of 0.920 g/cm³, hexene-copolymerized LLDPE generally shows higher dart impact, higher Elmendorf tear, and better hot-tack strength. Butene-copolymer grades retain a cost advantage and are suitable where ultimate toughness is not the controlling requirement. Compared with metallocene LLDPE of similar density, LL0335AA has a broader molecular weight distribution; this typically improves extrusion processability but reduces clarity and may reduce sealing performance on high-speed form-fill-seal lines. Within the Titanvene LLDPE range, the lower MFR of LL0335AA differentiates it from higher-flow grades such as LL0209AA by giving higher melt viscosity and greater bubble stability at the expense of maximum specific output.

    Regulatory Compliance and Migration Limits

    Because polyethylene is an olefin polymer, food-contact compliance is generally assessed under FDA 21 CFR 177.1520 in the United States and Regulation (EU) No 10/2011 in the European Union. Compliance is end-article dependent; a resin supplier may provide a statement of composition, but the converter is responsible for migration testing under the intended food simulant and temperature conditions. Heavy metals and restricted substances are covered through Directive 2011/65/EU and REACH EC 1907/2006. Supplier documentation should be requested for each lot and retained with the final film batch record.

    Regulatory areaStandard or regulationApplicability to LL0335AA
    Food contact, United States21 CFR 177.1520Olefin polymers may be used subject to prescribed extractable limits and end-use restrictions; final article compliance is converter-dependent.
    Food contact, European UnionRegulation (EU) No 10/2011Conformity requires verification of overall migration limit of 10 mg/dm² under specified food simulants.
    Heavy metals contentDirective 2011/65/EU Annex IIPolyethylene resins of this type are not expected to contain restricted substances above threshold limits; supplier certificate should be referenced.
    SVHC reportingREACH EC 1907/2006No Candidate List SVHCs are expected above 0.1 % w/w in the as-supplied pellet; article-level obligations remain with the converter.

    Storage, Drying, and Incompatibility Boundaries

    Titanvene LL0335AA pellets are hydrophobic and normally do not require predrying when protected from rain and condensation. If surface moisture is suspected after silo transfer or warehouse exposure, pellets can be dried at 60 °C to 70 °C for 2 h to 4 h in a desiccant or hot-air hopper dryer; temperatures above 80 °C may soften the pellet surface and cause bridging in the feed throat. Melt temperatures above 250 °C may promote gel formation and odour, while melt temperatures below 180 °C may produce unmelts or high die pressure. Regrind from edge trim is generally acceptable up to 20 % by mass, but corona-treated film regrind and printed trim can reduce seal strength and increase gel specks if introduced at higher levels. Avoid combining the resin with amine-based antifog or antistatic concentrates without prior compatibility testing because some amine additives can accelerate oxidative degradation in high-shear extrusion.

    Top