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Arkema Orevac® 18303S Maleic Anhydride modified LLDPE

    • Product Name: Arkema Orevac® 18303S Maleic Anhydride modified LLDPE
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 143256
    Productname Arkema Orevac 18303S
    Chemistry Maleic Anhydride modified LLDPE
    Form Pellets
    Density 0.920 g/cm³
    Meltflowrate 3.0 g/10 min at 190°C/2.16 kg
    Maleicanhydridecontent 0.3 wt%
    Meltingpoint 124 °C
    Vicatsofteningtemperature 92 °C
    Tensilestrengthatbreak 20 MPa
    Elongationatbreak 700%
    Flexuralmodulus 220 MPa
    Hardnessshored 52
    Thermalstability >250 °C
    Processingtemperature 180-240 °C

    As an accredited Arkema Orevac® 18303S Maleic Anhydride modified LLDPE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of Arkema Orevac® 18303S Maleic Anhydride modified LLDPE

    A five-layer blown film line running 55 µm total gauge places Orevac® 18303S between the internal polyamide or EVOH barrier ply and the polyethylene sealing plies. The resin is a maleic anhydride-grafted LLDPE with a nominal density of 0.912 g/cm³ measured to ISO 1183-1. Melt flow index is 1.5 g/10 min at 190 °C under 2.16 kg load per ISO 1133-1. Peak melting temperature is published near 123 °C under ISO 11357-3. The absolute maleic anhydride graft density is not disclosed in the manufacturer datasheet. Converter quality control relies on acid-base titration after xylene reflux hydrolysis or on carbonyl absorbance doublet integration by Fourier transform infrared spectroscopy. The tie layer is metered through a dedicated satellite extruder with 24:1 to 30:1 L/D ratio. Barrel temperature profile runs from 170 °C at the feed zone to 220 °C at the metering zone. Die exit melt temperature must not exceed 240 °C. Above this threshold, gel formation and free-maleic-odor release become measurable surface defects. The grafted maleic anhydride reacts with terminal amine groups on polyamide 6 and polyamide 66 and with residual hydroxyl groups on EVOH during melt contact in the combining adapter and die. The reaction is uncatalysed and proceeds within the air gap and post-die cooling section. Tie-layer thickness ranges from 3 to 8 µm. Below 2 µm, surface coverage of the barrier ply is incomplete and peel failures initiate along the coextrusion interface. Medium-barrier films routinely specify peel adhesion not less than 3 N/15 mm. High-barrier lidding, vacuum skin, and retort pouch structures demand 5 to 8 N/15 mm when tested according to ASTM F904-16 or ISO 11339. Polyamide must be pre-dried to less than 0.10 wt% moisture and EVOH to less than 0.30 wt% moisture before coextrusion. Moisture hydrolyses the polyamide and reduces available amine reaction sites at the interface. Film producers running at relative humidity above 60 % must maintain closed-loop resin delivery and hopper dryers at 80 °C for at least 4 h. Terminal converting outputs include vacuum pouches, MAP lidding film, cheese maturation bags, and heavy-duty sacks. The sealing ply must comply with food contact requirements under FDA 21 CFR §177.1520 for olefin polymers and under Regulation (EU) No 10/2011 total migration limit of 10 mg/dm² using food simulants assigned in Annex V. Because the tie layer is not the direct food contact surface, overall migration and specific migration of maleic acid are assessed on the finished article. The compliance matrix below identifies the relevant test obligations.

    Regulation or StandardScopeObligation in Finished Film
    FDA 21 CFR §177.1520Olefin polymers for food contactBase LLDPE sealing ply density, extractables, and end-use condition compliance
    Regulation (EU) No 10/2011 Annex IPlastic food contact materialsSML verification for maleic acid if migration is detectable; NIAS screening
    Regulation (EU) No 10/2011 Annex VCompliance testing protocolOverall migration 10 mg/dm² in simulants A, B, C and D2
    GB 4806.7Food contact plastic materials in ChinaOverall migration and consumption-specific limits for multi-material laminate films
    ASTM F88/F88MSeal strength of flexible barrier materialsHeat seal strength of the LLDPE sealing ply after hot-tack and sealing cycles
    ASTM F904-16Peel adhesion of laminatesT-peel adhesion at the barrier-to-sealant interface

    Where Halogen-Free Sheathing Compounds Exceed 60 wt% Mineral Loading

    Compounding of halogen-free flame-retardant cable sheathing grades begins with a base polymer mixture of LDPE, LLDPE, and ethylene-vinyl acetate copolymer containing 18 wt% vinyl acetate. Aluminium trihydroxide or magnesium dihydroxide is added at 55 to 68 wt% total loading. At these filler fractions, the zero-shear viscosity rises by more than one order of magnitude. The maleic anhydride groups on Orevac® 18303S undergo esterification with surface hydroxyl groups on the filler during the first kneading section of a co-rotating twin-screw extruder. Addition level is reported in compounder practice between 2 and 5 wt% of total compound. The functionalised polyolefin reduces filler-filler particle interaction. Torque reduction of 15 to 25 % has been observed on production-scale 44:1 L/D twinscrew lines with segmented screw geometry. The melt temperature window is narrow because aluminium trihydroxide begins releasing water of crystallisation near 180 to 220 °C. Free water creates internal bubbles and surface pinholes in the sheathing wall section. The compounder must hold melt temperature between 150 and 170 °C. Atmospheric or vacuum degassing is required in the second open barrel section at 20 to 60 kPa absolute pressure. Screw speed is typically set from 250 to 400 rpm. Lower speeds leave undispersed filler agglomerates. Higher speeds raise melt temperature above the filler dehydration threshold. Orevac® 18303S provides additional matrix-filler adhesion after melt solidification. This prevents particle pull-out during cable bending and cold impact. Elongation at break is measured according to ASTM D638 on dumbbells cut from compression-moulded plaques. Published cable standards set minimum elongation values that vary by voltage class and installation environment from 125 to 250 %. Smoke density is tested to IEC 61034-2. Halogen acid gas emission is assessed to IEC 60754-1. Flame propagation is evaluated under IEC 60332-1 for single insulated conductors and IEC 60332-3 for multi-core cable bundles. The coupling agent itself is halogen-free and contributes no acid gas. This is critical because acid gas limits under IEC 60754-1 are normally fixed below 0.5 % HCl equivalent. Terminal products include low-voltage building wire sheathing, solar cable jacketing, control cable sheathing, and mass transit conduit grades. Pre-compounded pellet moisture must remain below 500 ppm before extrusion. Higher moisture content causes surface roughness and reduces capstan line speed below commercial targets.

    FunctionTypical ComponentLoading Range (wt%)Relevant Test Method
    Base polymerLDPE / LLDPE / EVA 18% VA25 – 35ISO 1133-1, ISO 1133-1 shear viscosity
    Flame-retardant fillerCoated ATH, d50 1 – 2 µm55 – 68ISO 13320 laser diffraction
    Coupling agentOrevac® 18303S2 – 5FTIR graft verification by carbonyl absorbance
    Antioxidant systemHindered phenolic / phosphite / metal deactivator0.2 – 0.8ISO 11357-6 oxidative induction time
    Processing aidFluoropolymer-based friction modifier0.1 – 0.5Melt fracture elimination trial on 40 mm laboratory extruder

    Continuous lamination of aluminium coil to a 3 to 5 mm polyethylene core uses Orevac® 18303S as the interfacial adhesive component in both powder and granular forms. The aluminium skin, normally 0.30 to 0.50 mm thick, receives a chromate or chromium-free conversion coating before lamination. The maleic anhydride functionality chelates with aluminium oxide and hydrated aluminium species on the conversion-coated surface. Lamination temperature is set from 140 to 160 °C at the calendar roll nip. Press line speed is governed by the required peel adhesion after cooling. The laminated panel is tested to ASTM D903 for 180° peel and ASTM D1781 for climbing drum peel. National façade specifications such as GB/T 17748-2008 and EN 14509 define minimum values that depend on the panel class and fire rating. When the core is loaded with aluminium trihydroxide or magnesium dihydroxide for fire-rated B-s1,d0 or B1 façade panels, the same processing constraints described for halogen-free sheathing compounds reappear. Filler loadings can reach 65 wt%. Core compound melt temperature must be held between 150 and 165 °C to avoid filler dehydration. Residual moisture in the compound or surface moisture on the aluminium coil generates blisters at the metal-polymer interface. Coil storage above 60 % relative humidity requires inline drying of the aluminium surface at 90 to 110 °C for at least 30 seconds before the nip. Failure mode observed on field panels is progressive delamination from panel edges after 6 to 12 months of external exposure. This occurs when initial peel adhesion is below the jurisdiction minimum because interfacial hydration attacks the aluminium-grafted layer bond. The grafting reaction must be complete before the panel exits the continuous press. Insufficient residence time in the melt zone leaves unreacted maleic anhydride that later absorbs water. Terminal products include exterior cladding panels, signage substrates, and fire-rated interior partition panels. The powder grade of Orevac® 18303S reduces dust sensitivity during core layer spread application because the particle size distribution is controlled for electrostatic spraying and scatter coating.

    Steel Pipe 3LPE Coating — What Does the Interface Demand after 28 Days at 1.5 V?

    The three-layer external coating on buried steel pipe consists of a fusion-bonded epoxy primer, a maleic anhydride-grafted polyethylene adhesive layer, and a high-density polyethylene topcoat. Orevac® 18303S serves as the adhesive component or as a modifier blended with a low-melt-index HDPE in the middle layer. The steel pipe is blast-cleaned to surface preparation grade Sa 2.5 according to ISO 8501-1. The pipe is then inductively heated to 180 to 220 °C. Fusion-bonded epoxy powder is applied first. The epoxy layer, normally 150 to 300 µm, must reach a defined gel state before the adhesive layer is applied. If the epoxy crosslinks beyond the gel point before the grafted layer contacts it, the available hydroxyl groups are consumed inside the epoxy network. The grafted maleic anhydride layer then loses reactive sites for esterification with the epoxy interface. The adhesive layer is applied by side-wrap extrusion or through a crosshead die at 200 to 230 °C melt temperature. Thickness of the grafted adhesive layer ranges from 150 to 250 µm. The HDPE topcoat, 2.5 to 3.5 mm thick, is applied in the same pass. Adhesion qualification is performed after a 28-day cathodic disbondment test at 1.5 V in 3 % sodium chloride solution maintained at 23 °C per ISO 21809-1 and ASTM G42. Acceptance values in pipeline operator specifications commonly require disbondment radius not greater than 10 mm for three-layer systems. Long-term adhesion is further assessed by peel testing per DIN 30670 or by CSA Z245.21. The maleic anhydride-grafted middle layer must not be blended with amine-curable liquid epoxy additives. Free amines react prematurely with maleic anhydride and reduce the reactive site density at the FBE interface. Processing temperature must remain below 250 °C. Higher temperatures degrade the graft and release free anhydride volatiles that condense as oligomeric residue on the die face. Production-scale failure of 3LPE coated line pipe is most frequently detected as disbondment at the FBE-adhesive boundary after cathodic protection exposure. This failure results from either an over-cured epoxy primer or a grafted layer that was applied below 180 °C and failed to achieve sufficient interfacial melting. Terminal products include buried gas transmission pipelines, crude oil flowlines, water transmission mains, and offshore riser coating systems.

    Micropore Collapse Kinetics in 55 wt% CaCO₃-Filled Film after Machine-Direction Orientation

    In breathable film production, calcium carbonate-filled LLDPE is cast as a 40 to 60 µm precursor sheet. The filler loading is between 50 and 65 wt% with a coated calcium carbonate d50 of 1 to 3 µm. Orevac® 18303S is added at 2 to 4 wt% of total compound. The maleic anhydride groups react with fatty acid and hydroxyl functionalities on the carbonate surface. This improves filler wetting and reduces particle agglomeration before the orientation step. The precursor sheet is reheated and stretched in the machine direction at a draw ratio of 3:1 to 5:1 at 60 to 90 °C. Void initiation occurs at the polymer-filler interface when the matrix yield stress is exceeded. The grafted layer maintains a bonded interface that resists pore coalescence into splitting flaws. Without adequate coupling, the microvoids expand into continuous cracks running perpendicular to machine direction. This is a high-speed line defect that appears above 350 m/min. Water vapour transmission rate is measured to ASTM E398. Air permeability is measured with a Gurley densometer to ASTM D726. Tensile properties at break are measured to ASTM D882. Coupling level is adjusted so that Gurley air permeance and WVTR remain within the target window of the end product. A higher MAH-grafted resin concentration increases both tensile strength and void stability. It also raises the required motor load on the cast extruder if the screw is under-sized. The calcium carbonate must be dried to less than 0.10 wt% moisture before extrusion. Melt temperature is held from 200 to 240 °C at the flat die. Residual water converts to steam during cast film stretching and collapses freshly formed micropores. Terminal products include diaper backsheet, adult incontinence film, surgical drape film, housewrap, and protective packaging interleaving. The same compound formulation is processed into microporous battery separator precursor film when aperture uniformity and electrolyte wettability are critical. Published data specific to Orevac® 18303S in battery separator configurations is limited.

    In moisture-barrier lamination of LLDPE film to aluminium foil, Orevac® 18303S is compounded with aliphatic tackifier resin and paraffin wax into a solvent-free hot melt adhesive. The blend is applied at 170 to 200 °C through slot-die coating or roller coating. The maleic anhydride functionality bonds to hydrated aluminium oxide on the foil surface. Peel strength is measured to ASTM D1876 or ISO 11339. The crystalline LLDPE backbone limits cold-flex performance below 5 °C. The adhesive remains stiff at freezer temperatures. This restricts use in deep-freeze lamination where flexible polyolefin copolymers with lower crystalline melting points are preferred. The resin is not recommended for direct food contact adhesive layers unless the specific migration of maleic acid is confirmed below the applicable limit under Regulation (EU) No 10/2011. Terminal products include non-food industrial barrier laminates, insulation facing foil, and moisture-proof cable wrap. Published data specific to Orevac® 18303S in hot melt adhesive formulations is limited to customer technical trials; no standardised public database exists for peel retention after moisture ageing.

    Polyamide Contamination in Post-Industrial Scrap Alters the Processing Window Below 5 wt%

    Post-industrial trim from five-layer packaging lines contains dispersed polyamide and EVOH particles. When this scrap is recycled into blown LDPE film, the polyamide forms incompatible domains that create gels, pinholes, and melt-pressure instability. Orevac® 18303S is added at 2 to 4 wt% in a re-granulation step on a twin-screw extruder with 36:1 L/D ratio and low-shear screw configuration. The maleic anhydride groups react with polyamide terminal amines at the domain surface. This reduces interfacial tension and disperses polyamide into sub-10 µm domains. This is verified by light microscopy on compression-moulded thin sections and by filtration-pressure rise testing in a single-screw extruder. The recycled film maintains dart impact and tear properties acceptable for refuse sacks, construction film, and secondary packaging. The compatibility mechanism is not effective above 5 wt% polyamide contamination. Above this threshold, the dispersed phase volume exceeds the reactive capacity of the grafted resin at the stated addition level. Higher addition levels are technically possible but raise compound cost beyond the economic value of the regrind stream. Melt temperature during re-granulation is held from 190 to 220 °C. Lower temperatures do not complete the ester-amidation reaction. Higher temperatures degrade the graft. The re-granulated material is then blended with virgin LDPE at 20 to 50 wt% regrind addition. Film performance is tested to ASTM D1709 for dart drop impact and ASTM D1922 for Elmendorf tear. The recycled fraction must be filtered through 80 to 120 mesh screens to remove unmelted polyamide particles larger than 100 µm. Terminal products include waste collection sacks, protective furniture wrap, industrial liner film, and shrouding for palletised freight.

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