| HS Code | 205524 |
| Productname | Bio-polyolefins 2002D Starch-Based Clear Extrusion Compostable Grade |
| Grade | 2002D |
| Materialtype | Starch-based bio-polyolefin |
| Appearance | Clear |
| Form | Pellets |
| Processingmethod | Extrusion |
| Compostability | Compostable |
| Biobasedcontent | ≥50% |
| Density | 1.20 g/cm³ |
| Meltflowrate | 2.0 g/10 min |
| Tensilestrength | 20 MPa |
| Elongationatbreak | 300% |
| Flexuralmodulus | 500 MPa |
| Vicatsofteningpoint | 80 °C |
| Heatdeflectiontemperature | 55 °C |
| Moisturecontent | <1% |
| Shelflife | 12 months |
| Storageconditions | Cool, dry place |
| Compostingstandard | EN 13432 / ASTM D6400 |
As an accredited Bio-polyolefins 2002D Starch-Based Clear Extrusion Compostable Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in 25 kg moisture-resistant paper bags, palletized and shrink-wrapped, ensuring safe storage and transport for this compostable grade. |
| Container Loading (20′ FCL) | 20′ FCL container loading: palletized 25 kg bags of Bio-polyolefins 2002D starch-based clear compostable extrusion grade, stretch-wrapped, secured for export. |
| Shipping | Bio-polyolefins 2002D Starch-Based Clear Extrusion Compostable Grade typically ships as non-hazardous resin pellets in moisture-barrier bags on pallets. Transport in clean, dry vehicles at ambient temperature, avoiding direct sunlight, moisture, contamination, and sharp objects. Not DOT/IMDG/IATA regulated. Store sealed in a cool, dry area until use. |
| Storage | Store Bio-polyolefins 2002D Starch-Based Clear Extrusion Compostable Grade in a cool, dry, well-ventilated warehouse, away from direct sunlight, heat, and moisture. Keep in sealed original packaging on pallets. Avoid contact with strong oxidizers and contaminants. Maintain moderate humidity and ambient temperature. Protect from pests and physical damage. Use first-in, first-out stock rotation; do not exceed safe stacking limits. Reseal opened packages promptly. |
| Shelf Life | Shelf life is 12 months from manufacture when stored unopened in original packaging below 50°C and 50% relative humidity. |
The blown-film conversion of Bio-polyolefins 2002D into transparent flow-wrap for low-moisture foods requires the resin to be predried to <0.1% moisture before the hopper because the starch phase hydrolyzes at melt temperatures above 160 °C, generating volatile acidic species and melt-pressure oscillation. On a grooved-feed single-screw extruder with L/D 30:1, compression ratio 3:1, and a Maddock shear mixer, the temperature profile is maintained between 145 °C and 160 °C in barrel zones 1–3 and 155–165 °C at the die; excursion above 175 °C produces die-lip build-up and pinholes in film below 20 µm. Formulation addition ratios of 30–45 wt% are typical when the 2002D grade is let down with PBAT and a PLA nucleation package, with 0.3–0.8 wt% erucamide slip and 0.2–0.5 wt% silica antiblock added to control blocking after corona treatment to a wetting tension of 38–42 mN/m. Melt-flow-index of the dried compound measured at 190 °C/2.16 kg per ISO 1133-1:2022 is maintained at 3–6 g/10 min for bubble stability. Terminal product types include pillow-pack flow-wrap for crackers, wafer sleeves, dry cereal bars, and low-fat snack pouches with water activity below 0.6. Compliance requires final-article testing under EN 13432:2000, including ≥90% aerobic biodegradation by ISO 14855-1:2012 within 180 days, disintegration by ISO 16929:2021, and heavy-metal limits per EN 13432:2000. Food-contact assessment follows EU Regulation 10/2011, with overall migration ≤10 mg/dm² under simulant A for dry foods; U.S. clearance is formulation-specific under 21 CFR 170.100 Food Contact Notification. On production lines, blocking at the winder is observed when film surface temperature exceeds 35 °C before lay-flat cooling; chill-roll temperature setpoints of 18–22 °C and bubble air temperature of 12–18 °C are used to stabilize gauge variation.
Retail produce bag conversion exposes the 2002D grade to thinner gauges and higher blow-up ratios than flow-wrap; the limiting parameter is no longer dispersion but melt strength at the frost line. In formulations containing 25–38 wt% Bio-polyolefins 2002D, the remaining phase is typically 55–65 wt% PBAT and 7–12 wt% PLA or PBS, with 0.1–0.3 wt% slip and 0.2–0.6 wt% antiblock. Raising the starch phase above 38 wt% reduces film tensile elongation at break below 200% in machine direction when tested by ASTM D882-18 and lowers Elmendorf tear below 3.5 N/mm in transverse direction as measured by ASTM D1922-15; the resulting film splits during perforation and bag dispensing. The downstream process uses a high-blow-up-ratio blown-film line with die diameter 150–250 mm, die gap 0.8–1.2 mm, blow-up ratio 3.0–4.0:1, and internal bubble cooling. Barrel zone temperatures are kept at 140–155 °C to avoid pre-foaming of residual moisture; head pressure is sustained at 120–180 bar by a barrier screw with L/D 30:1. Terminal product types include T-shirt produce bags, roll bags for leafy greens, wet-vegetable perforated bags, and industrial-compostable kitchen caddy liners. Compliance anchors are EN 13432:2000 for industrial compostability, ASTM D6400-19 for North American compostability claims, and EU Regulation 10/2011 for food-contact migration; U.S. food-contact status is established through a formulation-specific 21 CFR 170.100 Food Contact Notification. Batch-to-batch variance in moisture content above 0.15% by Karl Fischer titration has been observed to produce gel counts above 15 particles/m² and visible fish-eye defects in lay-flat; hopper-dryer air dew point should remain below -40 °C. Dart-impact values measured by ASTM D1709-16a are typically 80–120 g for 15 µm film, but drop below 60 g when the 2002D phase exceeds 38 wt% or when the blow-up ratio is reduced below 2.6:1.
Comparative downstream process and formulation matrix:
| Segment | 2002D addition ratio | Primary process window | Primary regulatory anchor |
|---|---|---|---|
| Transparent flow-wrap film | 30–45 wt% | 145–165 °C; blow-up ratio 2:1–3:1 | EN 13432:2000; EU Regulation 10/2011 |
| Produce bag and caddy liner | 25–38 wt% | 140–155 °C; blow-up ratio 3:1–4:1 | ASTM D6400-19; EU Regulation 10/2011 |
| Agricultural mulch film | 15–25 wt% | 150–170 °C cast film; 15–40 µm gauge | EN 17033:2018; EN ISO 17556:2019 |
| Paper extrusion coating | 25–40 wt% | 150–165 °C; air gap 80–150 mm | FDA 21 CFR 176.170(c); EU Regulation 10/2011 |
| Thermoformed clear tray | 20–30 wt% | Sheet die 185–200 °C; forming 90–110 °C | EN 13432:2000; EU Regulation 10/2011 |
| Shrink film | 20–35 wt% | First bubble 140–160 °C; orientation 60–70 °C | EN 13432:2000; ISO 527-3:2018 |
In agricultural soil-contact applications, the processing window narrows because the 2002D grade must produce a film that resists field wind loads and still fragments after soil incorporation by a rotary tiller. Formulations for clear compostable mulch film typically use 15–25 wt% Bio-polyolefins 2002D in a PBAT/PLA carrier; higher starch fractions above 25 wt% reduce tear propagation resistance below 2.5 N/mm measured by ASTM D1922-15 and create premature splitting at planting holes. The compound is processed on a cast-film line at melt temperatures of 150–170 °C, die gap 0.6–1.0 mm, and chill-roll temperature 15–20 °C; gauge is controlled at 15–25 µm for row-crop use and 25–40 µm for low-tunnel covers. Terminal product types include transparent soil-warming mulch for solanaceous and cucurbit crops, micro-perforated clear mulch for lettuce, and low-tunnel film that is removed from the field and composted separately or soil-incorporated where the standard allows. The primary compliance anchor is EN 17033:2018, which requires aerobic soil biodegradation by EN ISO 17556:2019 at 90% relative degradation within 24 months, plus eco-toxicity testing after soil exposure. Because clear films permit weed germination, agronomic use typically pairs the film with pre-emergence herbicide or flame weeding before planting; this operational limitation is not altered by resin chemistry. UV stabilization is restricted to additives that do not exceed heavy-metal limits under EN 13432:2000, since the film is intended for soil degradation. Field trials indicate that fragmentation begins at 90–150 days depending on soil temperature and microbial activity; published data for the 2002D grade in this specific configuration is limited, and processors validate film-level endpoint on local soil.
Extrusion coating with the 2002D grade replaces a non-compostable polyolefin coating on paper and paperboard, but the line must be reconfigured because starch-based melts exhibit lower thermal stability and narrower adhesion windows than LDPE. Coating layer formulations contain 25–40 wt% Bio-polyolefins 2002D, 55–70 wt% PBAT, and 0–10 wt% PLA as a stiffness modifier; additives include 0.2–0.5 wt% erucamide and 0.1–0.3 wt% antioxidant. The downstream process uses a single-screw extruder with L/D 30:1, barrier screw, and flat die with 0.4–0.7 mm die gap; melt temperature is held at 150–165 °C, and the air gap is minimized to 80–150 mm to limit oxidative gel formation. Coating weight is controlled at 15–25 g/m² for hot-beverage cups and 25–35 g/m² for tray board; line speed is limited to 80–150 m/min by pinholing caused by moisture escaping from the paper substrate. Terminal product types include compostable paper cups for hot drinks, cold-beverage paper cups, paper plates, and clamshell paperboard food containers. Regulatory compliance for food contact is evaluated under FDA 21 CFR 176.170(c) for paperboard coatings and EU Regulation 10/2011 for overall migration; compostability of the coated article is tested under EN 13432:2000 with disintegration per ISO 16929:2021. Adhesion failure at the paper-coating interface is observed when paper moisture exceeds 7% or when melt temperature drops below 145 °C; corona pretreatment of the paperboard at 38–42 mN/m wetting tension is required before extrusion.
Compliance checklist for compostable packaging conversion:
| Control point | Method or standard | Acceptance criterion | 2002D grade implication |
|---|---|---|---|
| Aerobic biodegradation of final packaging article | ISO 14855-1:2012 | ≥90% relative degradation in 180 days | Starch phase accelerates early mineralization; polyester phase controls the later plateau. |
| Compost disintegration | ISO 16929:2021 | ≥90% of particles 2 mm after 12 weeks | Thin films below 50 µm disintegrate faster than rigid trays; sheet thickness above 0.8 mm may require longer under standard conditions. |
| Heavy metals | EN 13432:2000, Annex E | Below listed limits for Zn, Cu, Ni, Cd, Pb, Hg, Cr, Mo, Se, As, F | Additive selection must avoid metal-based nucleants and certain colorants. |
| Food contact – plastic film | EU Regulation 10/2011; 21 CFR 170.100 FCN | Overall migration ≤10 mg/dm²; FCN clearance for intended food types | Migration testing must be conducted on the final compounded film, not on neat resin. |
| Food contact – coated paper | FDA 21 CFR 176.170(c); EU Regulation 10/2011 | Extractive limits for aqueous and fatty foods; overall migration ≤10 mg/dm² | Coating weight and pinhole density determine barrier and migration compliance. |
| Soil biodegradation for mulch film | EN ISO 17556:2019 under EN 17033:2018 | ≥90% in 24 months at 20–28 °C | Clear films with starch phase show faster initial fragmentation but must pass eco-toxicity endpoints. |
Sheet extrusion and subsequent thermoforming of the 2002D grade into rigid clear produce trays require balancing PLA stiffness against starch-phase processability. In sheet formulations, the starch-based component is limited to 20–30 wt%, while PLA at 60–70 wt% provides modulus and 5–10 wt% PBAT provides impact modification. The compound is prepared on a co-rotating twin-screw extruder with L/D 40:1 and vacuum devolatilization at -0.08 MPa; melt temperature at the die is 185–200 °C for PLA-rich systems, which exceeds the 2002D thermal limit unless the starch phase is fully encapsulated by the polyester matrix. Flat-die sheet line uses a 0.3–0.8 mm die gap and three-roll stack temperatures of 40–60 °C. Thermoforming is conducted at sheet surface temperatures of 90–110 °C using aluminum molds heated to 30–50 °C; the processing window is narrow because below 88 °C microcracks initiate at the starch-polyester interface and above 115 °C PLA crystallinity causes haze and embrittlement. Terminal product types include clear berry clamshells, cherry tomato trays, mushroom punnets, and single-serve salad bowls with wall thickness 0.25–0.50 mm. Compliance under EN 13432:2000 requires that the final thermoformed article disintegrates under ISO 16929:2021 with no more than 10% residue on a 2 mm sieve after 12 weeks; European food-contact compliance follows EU Regulation 10/2011 with overall migration ≤10 mg/dm². In U.S. contexts, food-contact status is established through a formulation-specific 21 CFR 170.100 Food Contact Notification, and compostability claims follow ASTM D6400-19. On manufacturing lines, the dominant defect is sheet sag during thermoforming when PLA crystallinity exceeds 40%; control of roll-stack temperature and sheet moisture below 0.1% is essential.
Double-bubble orientation of starch-based clear extrusion compounds is constrained by the narrow window between orientation temperature and the onset of heat-set crystallinity. In shrink-film trials, formulations containing 20–35 wt% Bio-polyolefins 2002D, 55–70 wt% PBAT, and 5–10 wt% PLA are first extruded on a single-screw line with L/D 30:1 at 140–160 °C into a thick primary tube, then quenched to 20–25 °C. The primary tube is reheated to 60–70 °C and inflated in the second bubble to a transverse orientation ratio of 3.0–4.0:1 and a machine-direction draw ratio of 2.0–3.0:1; resulting shrink films at 30–50 µm achieve 40–55% shrinkage at 80 °C in water bath tests. Terminal product types include tamper-evident bands for compostable bottles, sleeve labels for dry-goods containers, and collation shrink film for multipacks of lightweight products. Published data for the 2002D grade in double-bubble lines is limited; processors must confirm that the starch phase does not form gel particles larger than 50 µm during the reheating step. Compliance for compostability is tested under EN 13432:2000 and ASTM D6400-19; food-contact sleeves are assessed under EU Regulation 10/2011 when the label is not separated from the package before disposal. Film tensile properties are measured by ISO 527-3:2018, with typical machine-direction elongation above 300% before shrinking.
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Bio-polyolefins 2002D Starch-Based Clear Extrusion Compostable Grade is a pelletized thermoplastic compound supplied for cast film, blown film, and sheet extrusion. The material is formulated with starch-based domains dispersed in a polyolefin matrix. The starch phase provides enzymatic access during industrial composting, while the polyolefin phase contributes melt processability, seal strength, and web handling. Product-specific lot documentation should be obtained from the supplier before line trials because starch dispersion, moisture uptake, and additive levels vary between production campaigns.
Model designation 2002D identifies the grade as a clear extrusion product within the bio-polyolefin series. Unlike conventional polyolefins, the material is designed to fail compostability screening only when starch domains remain accessible and oxidative fragmentation of the polyolefin is not inhibited. This dual mechanism distinguishes 2002D from purely starch-based thermoplastic starch grades, which are more moisture-sensitive and less melt-stable, and from fully bio-based polyesters, which differ in sealing behavior and modulus.
Compostability claims for Bio-polyolefins 2002D are evaluated under EN 13432:2000, which requires characterization, biodegradation, disintegration, and ecotoxicity testing. Ultimate biodegradation is measured by ISO 14855-1:2012 under controlled composting conditions at 58 ± 2 °C. A passing grade must reach at least 90% carbon conversion to CO₂ within 180 days. Disintegration is assessed by ISO 16929:2019, with a criterion of 90% of the material passing a 2 mm sieve after 12 weeks. Ecotoxicity screening follows OECD 208:2006 and DIN EN 13432 Annex E, using plant emergence and growth tests on compost residues. Heavy metal limits are set by EN 13432:2000 Table A.1.
The starch-rich domains in 2002D are hydrolytically and enzymatically attacked by compost microbiota. The polyolefin fraction undergoes abiotic oxidation followed by mineralization. This mechanism is slower than bulk hydrolysis of PLA and more dependent on surface area and film thickness. Certification bodies such as DIN CERTCO and TÜV Austria require batch-specific evidence of compliance before OK compost industrial or seedling mark use is permitted. Labeling claims must reference the exact certification number and the compostability standard because home compost conditions do not reliably meet the temperature and moisture requirements of EN 13432:2000.
Rheological characterization of the 2002D grade is performed according to ISO 1133-1:2022 at 190 °C with a 2.16 kg load. Melt volume-flow rates for starch-modified polyolefin extrusion grades commonly occupy a 2–8 cm³/10 min band; for this grade, the supplier’s certificate should be consulted because starch content and residual moisture shift values. Density determined by ISO 1183-1:2019 typically falls between 1.05 g/cm³ and 1.25 g/cm³. Tensile properties measured on 1 mm compression-molded sheets under ISO 527-3:2018 show machine-direction tensile strengths in the 12–25 MPa range and elongation at break of 150–400%. Moisture content before processing is controlled below 0.1% by Karl Fischer titration under ISO 15512:2019. Biobased carbon content measured by ASTM D6866-22 Method B typically falls between 30% and 60%, depending on the starch loading and whether the polyolefin matrix contains renewable feedstocks.
Published data for this specific 2002D configuration is limited; the stated intervals are representative of starch-filled polyolefin extrusion grades characterized under similar protocols. For lot release, converters should request melt volume-flow rate, density, moisture, and tensile data from the supplier. Batch-to-batch variance is often dominated by starch source particle size distribution and moisture history. Granules stored in humid air above 60% relative humidity can pick up water and should be re-dried before processing. Granule geometry and bulk density are not specified in the standard datasheet but affect feeding consistency. Converters should verify bulk density under ISO 60:1977 and flowability on hopper loaders. For clear film, optical control includes haze measurement under ISO 14782:2021 and transmittance under ISO 13468-1:2019. A haze value below 10% on 40 µm film is typical for clear starch-polyolefin compounds when starch domains remain below 400 nm; values above 20% indicate poor dispersion or moisture-induced hydrolysis during processing.
| Parameter | Test method | Typical acceptance criterion |
|---|---|---|
| Density | ISO 1183-1:2019 | 1.05–1.25 g/cm³ |
| Melt volume-flow rate | ISO 1133-1:2022 | 2–8 cm³/10 min |
| Tensile strength | ISO 527-3:2018 | 12–25 MPa |
| Elongation at break | ISO 527-3:2018 | 150–400% |
| Moisture content | ISO 15512:2019 | <0.1% |
| Biobased carbon | ASTM D6866-22 | 30–60% |
| Disintegration | ISO 16929:2019 | ≥90% in 12 weeks |
| Biodegradation | ISO 14855-1:2012 | ≥90% in 180 days |
Extrusion-grade starch composites differ from polylactic acid and polybutylene adipate terephthalate in matrix chemistry and failure behavior. PLA melts near 150–160 °C and provides high modulus but limited tear resistance and slow crystallization at film gauge below 30 µm. PBAT offers high elongation but lower modulus and higher blocking tendency. Bio-polyolefins 2002D combines a polyolefin matrix with dispersed starch domains; clarity depends on maintaining domain sizes below 400 nm and refractive index contrast below the visible wavelength limit. In blown film trials, haze development increases when starch particles exceed 1 µm, which can occur under low shear or with moisture above 0.2%.
Unlike PLA, the 2002D grade can be sealed on standard polyolefin sealing jaws without embrittlement at 120–140 °C. Unlike PBAT, it exhibits lower surface tack and better web release on cast chill rolls. However, the starch phase lowers water vapour barrier compared with neat polyolefins, and the grade is not a barrier polymer. It also retains a fossil-derived fraction, so it does not meet all renewable carbon targets that fully bio-based polyesters may satisfy. Certification for food contact is not automatic; compliance with FDA 21 CFR 176.170 or EC 10/2011 must be confirmed for each formulation and food type. The grade is not classified as an oxo-degradable material under EU Directive 2019/904. Unlike oxo-degradable polyolefins that fragment into microplastics, 2002D is designed for industrial composting.
| Property or behavior | Bio-polyolefins 2002D | PLA | PBAT | LDPE |
|---|---|---|---|---|
| Matrix chemistry | Starch-filled polyolefin | Polyester | Copolyester | Polyolefin |
| Melt processing window | 150–190 °C | 160–200 °C | 120–160 °C | 160–240 °C |
| Moisture sensitivity | High, pre-drying below 0.1% | High, pre-drying below 0.025% | Moderate | Low |
| Compostability certification basis | EN 13432:2000, ISO 14855-1:2012 | EN 13432:2000, ASTM D6400-21 | EN 13432:2000 | Not compostable |
| Clarity control variable | Starch domain size below 400 nm | Crystallinity and additive loading | Amorphous phase compatibility | Branching and chill roll temperature |
| Seal initiation range | 120–140 °C | 85–100 °C | 90–110 °C | 105–125 °C |
Starch begins to undergo thermal decomposition above 180 °C with glycosidic bond scission, dehydration, and caramelization. In the 2002D grade, melt temperatures above 190 °C generate reducing sugars and organic acids that accelerate polyolefin chain scission. Thermogravimetric analysis under ISO 11358-1:2022 typically shows a two-stage mass loss: starch decomposition between 280 °C and 350 °C, and polyolefin decomposition above 400 °C. The practical processing limit is lower than the onset of rapid mass loss because viscosity reduction and colour formation precede char formation.
Barrel residence time is a controlling variable. At 180 °C, residence times below 3 min are recommended to limit starch degradation. Screw configurations with low-shear mixing elements reduce viscous heating and prevent localized temperature spikes. Filter packs should be sized to avoid pressure-induced overheating; melt screens upstream of the die should be 100 mesh or coarser to prevent gel accumulation.
Direct replacement of low-density polyethylene in transparent packaging extrusion requires adjustment of barrel temperatures, screw speed, and die gap because the starch-filled polyolefin exhibits lower melt strength and a narrower thermal degradation window. On single-screw extruders with grooved feed sections and 30:1 L/D, a barrel temperature profile from 150 °C at the feed zone to 180 °C at the metering zone is used. Die temperature is maintained at 160–180 °C, and melt temperature is held below 190 °C to avoid starch caramelization and volatile generation.
Pre-drying in a desiccant dryer at 70 °C for 4 h reduces moisture to below 0.1%. For blown film, die gap settings of 1.2–2.0 mm and blow-up ratios between 2.5:1 and 3.5:1 are employed. Cast film lines running monolayer structures at 30–40 µm thickness use chill roll temperatures of 20–40 °C to control clarity and web flatness. Production-scale twin-screw compounding with 36:1 L/D has shown that starch aggregation increases screen changer pressure when pre-drying is omitted or when moisture exceeds 0.2%. Shutdown procedures should include purging with a low-melt-index polyolefin to prevent starch residue from charring in the die.
The lower melt strength of starch-filled polyolefins compared with LDPE at equivalent melt index restricts maximum line speed and bubble stability. Use of an internal bubble cooling system or a low stalk height is required on high-output blown film lines. Draw resonance in cast film can be controlled by maintaining the melt temperature at the upper end of the recommended window and by increasing die lip opening. However, raising melt temperature above 190 °C accelerates starch thermal degradation, liberates volatile compounds, and produces gel-like defects. This narrow temperature window is the primary processing conflict for converters accustomed to LDPE.
Typical use cases include clear compostable produce bags, carrier bags, and secondary packaging films where industrial compostability is required by local regulation. The grade is evaluated on monolayer structures at 30–40 µm gauge. Multilayer constructions may be possible with tie resins and barrier layers, but compostability of the final structure must be reassessed under EN 13432:2000 because individual component certifications do not automatically transfer.
Operational boundaries for the 2002D grade include storage in sealed containers at relative humidity below 60% and avoidance of amine-based additive packages that accelerate starch discoloration. Pro-oxidant systems containing transition metal stearates should not be added above 0.5 wt% because they can initiate uncontrolled oxidative chain scission and reduce shelf life. The grade is not suitable for multilayer structures requiring high oxygen barrier unless paired with a barrier layer such as EVOH, and published data for this specific configuration is limited for retort or hot-fill applications.
Film converters evaluating seal integrity should apply ISO 527-3:2018 tensile characterization and ISO 6383-2 tear propagation resistance on cast film samples, with lot-to-lot variation monitored for melt flow and moisture content before startup. Extrusion equipment should be purged before shutdown, and regrind ratios above 20% are not recommended unless drying is verified, because reprocessing shifts melt flow and increases yellowing.