| Код ТН ВЭД | 440794 |
Как аккредитованный Mitsubishi ROLASERIT PBT01 PBT 3D Printing Powder завод, мы соблюдаем строгие протоколы качества - каждая партия подвергается строгим испытаниям для обеспечения последовательных стандартов эффективности и безопасности.
| Упаковка | Mitsubishi ROLASERIT PBT01 PBT 3D Printing Powder, 1 kg, packaged in a sealed moisture-barrier foil bag within a cardboard box. |
| Погрузка контейнера (20-футовый контейнер) | 20′ FCL container loading of Mitsubishi ROLASERIT PBT01 PBT 3D printing powder, palletized, moisture-protected, and securely braced for ocean shipment. |
| Доставка | Mitsubishi ROLASERIT PBT01 PBT 3D Printing Powder is shipped as a non-hazardous, moisture-sensitive thermoplastic powder in sealed moisture-barrier packaging. Store and transport dry, cool, and ventilated, away from ignition sources. Avoid dust inhalation; follow supplier SDS and local transport regulations. Use antistatic liners and keep containers closed. |
| Хранение | Store Mitsubishi ROLASERIT PBT01 PBT powder in a cool, dry, well-ventilated place, away from heat, sparks, open flames, and sunlight. Keep original containers tightly closed to prevent moisture absorption and dust escape. Avoid static discharge and strong oxidizers. Use grounded equipment, maintain clean conditions, and follow the manufacturer’s SDS. Do not store near food, drink, or incompatible materials. Protect containers from damage. |
| Срок годности | Mitsubishi ROLASERIT PBT01 PBT powder shelf life: 12 months when stored unopened, cool, dry, protected from moisture, heat, and sunlight. |
Engineered connectors installed within 150 mm of the exhaust gas recirculation housing in Euro 6d diesel platforms require continuous service at 130 °C to 140 °C with transient excursions to 160 °C during active DPF regeneration cycles. Sintered PBT01 specimens conditioned at 23 °C and 50% relative humidity per ISO 62-4 absorb approximately 0.1% moisture by mass. This moisture uptake maintains volume resistivity above 10¹² Ω·cm when measured according to IEC 62631-3-1. Build chamber temperature is held at 196 °C to 202 °C with laser energy density controlled within 0.09 J/mm² to 0.11 J/mm². Layer thickness of 120 µm produces interlayer fusion sufficient to withstand 1,500 thermal shock cycles from -40 °C to +125 °C per ISO 16750-4 without crack propagation exceeding 0.3 mm. Production-scale experience on EOS P396 systems indicates that bulk powder after three complete build cycles shows a melt flow rate shift of less than 8% when measured at 250 °C with 2.16 kg load per ISO 1133-1:2022. Connector locking tabs printed at 0° build orientation require a minimum unsintered powder removal routine using compressed air at 0.6 MPa followed by ultrasonic cleaning in deionized water at 40 kHz for 120 seconds. The semi-crystalline nature of PBT creates the primary processing conflict. Shrinkage anisotropy between in-plane and through-thickness dimensions measures 1.8% to 2.4% versus 0.9% to 1.2% respectively when measured per ISO 294-4. Warpage on connector bodies longer than 60 mm must be corrected by build orientation rotation at 15° increments. Batch-to-batch variance in melt enthalpy greater than 5% of nominal value requires build chamber setpoint adjustment of ±2 °C to maintain consistent edge definition on snap-fit features. Pre-drying of recycled powder at 110 °C for 5 hours is mandatory when storage relative humidity exceeds 60% for more than 48 hours. A virgin-to-recycled powder blend ratio of 60:40 by mass is maintained for under-hood connector production.
| Standard | Clause / Test Method | Measured Property | Acceptance Criterion | Verification Equipment |
|---|---|---|---|---|
| ISO 16750-4 | Clause 5.3.2 Thermal Shock | Crack propagation | ≤ 0.3 mm after 1,500 cycles | Dual-chamber thermal shock |
| IEC 62631-3-1 | Method 2 Volume Resistivity | Insulation resistance | ≥ 10¹² Ω·cm | High-resistance electrometer |
| ISO 62-4 | Method 2 Water Absorption | Moisture uptake | ≤ 0.2% by mass | Analytical balance |
| USCAR-2 | Paragraph 5.2.3 Contact Resistance | Terminal contact resistance | ≤ 10 mΩ after 100 cycles | Micro-ohmmeter |
| LV214 | Section 4.3 Vibration | Connector contact integrity | Severity level 3, no discontinuity > 1 µs | Multi-axis vibration system |
| ISO 6722-1 | Insulation thickness verification | Wall thickness | No section below minimum | Optical microscope |
Comparative tracking index retention in sintered PBT relay bases is governed by residual porosity at the part surface and the thermal degradation products formed during the laser scan pass. Relay base designs with creepage distances below 3.2 mm per IEC 60664-1 Pollution Degree 2 require CTI values exceeding 175 V when measured per IEC 60112. Unfilled PBT powder sintered at 0.09 J/mm² typically delivers CTI in the 250 V to 400 V range. However, surface porosity of 2% to 4% creates conductive path initiation sites when electrolyte contamination from flux residues is present. The laser scan pass generates localized thermal degradation products. These products migrate to the part surface during cooling. They reduce effective tracking resistance by up to 20% when compared with injection-molded PBT of equivalent formulation. Build orientation of terminal blocks at 30° relative to the recoater blade direction minimizes surface roughness on creepage-critical faces. Surface roughness Ra values of 8 µm to 12 µm measured per ISO 4287 demand post-process infiltration with a low-viscosity epoxy sealant to achieve UL 94 V-0 listing at 0.75 mm wall thickness. The sealant is mixed at a 2:1 resin-to-hardener ratio by mass and cured at 60 °C for 90 minutes. Unsealed sintered surfaces typically achieve UL 94 V-2 when tested per IEC 60695-11-10. Production-scale experience on Farsoon HT252P systems indicates that relay bases sintered without sealant fail dielectric withstand testing per IEC 60664-1 at 3.0 kV AC for 60 seconds when relative humidity during storage exceeds 70% for 14 days. Pre-drying of the powder at 110 °C for 5 hours is mandatory before sintering. Published data for CTI retention after repeated SLS recycling of PBT01 beyond three complete build cycles is limited. Terminal blocks with integrated snap-fit retention features must avoid build orientations that place the snap-fit flexural axis parallel to the layer plane. Flexural cracks initiate at layer interfaces when strain exceeds 1.5%. Terminal block bases requiring integrated threaded brass inserts specify hole diameters of 3.8 mm to 4.0 mm before heat-staking at 200 °C insert temperature.
In low-volume electronic assembly lines, sintered PBT01 at 120 µm layer thickness replaces machined polyoxymethylene for production jigs when fixture service temperature exceeds 100 °C, machining lead time exceeds 8 days, and dimensional tolerance of ±0.25 mm is acceptable per ASME Y14.5. Pre-drying at 110 °C for 5 hours is required when storage relative humidity exceeds 60% to prevent steam-induced porosity at the melt pool interface.
Porosity measurements on sintered PBT01 fluid manifold prototypes using mercury intrusion porosimetry per ASTM D4404 reveal open pore fractions of 2.5% to 5.0% at 120 µm layer thickness. This porosity prevents direct use of as-sintered manifolds for pressurized liquid applications without post-process sealing. Hydrocarbon permeation testing per ASTM D814-95 on 3 mm wall specimens exposed to ASTM Fuel C at 60 °C shows mass gain of 0.5% to 1.2% after 24 hours. This absorption behavior mirrors injection-molded PBT. Differential pressure testing at 0.5 MPa air pressure using ASTM D1599 methodology produces visible bubble leakage at seal interfaces unless surfaces are machined flat to 1.6 µm Ra per ISO 4287. Machining of sintered PBT01 is performed on high-speed CNC spindles at 20,000 rpm with carbide end mills. Published data for this specific PBT01 configuration in continuous hydrocarbon immersion beyond 72 hours is limited. Layer plane permeability exceeds through-thickness permeability by a factor of 3 to 5. Manifold prototypes intended for coolant flow validation under 0.3 MPa pressure at 90 °C require vacuum impregnation with methacrylate sealant per MIL-STD-276. This sealant cures at 80 °C for 45 minutes. Sealed manifolds withstand 500 thermal cycles from 25 °C to 90 °C with coolant exposure without pressure decay exceeding 0.02 MPa per cycle. Build chamber temperature uniformity of ±2 °C across the 500 mm × 500 mm build area is required. Temperature gradients above ±3 °C produce warpage exceeding 0.4 mm on manifold bodies longer than 120 mm. The warpage is measured on a granite surface plate per ISO 1101. Wall thickness below 2 mm is not recommended for pressurized fluid contact due to pore interconnectivity across the entire cross-section.
| Parameter | PBT01 at 120 µm layer | PBT01 at 100 µm layer | Injection-molded PBT |
|---|---|---|---|
| Open porosity (ASTM D4404) | 2.5% – 5.0% | 1.8% – 3.5% | ≤ 0.5% |
| Layer-plane permeability ratio | 3× – 5× higher | 4× – 6× higher | Not applicable |
| Surface roughness Ra (ISO 4287) | 8 µm – 12 µm | 6 µm – 9 µm | 0.4 µm – 0.8 µm |
| Mass gain in ASTM Fuel C, 24 h | 0.5% – 1.2% | 0.5% – 1.2% | 0.4% – 0.9% |
When a device housing contacts intact skin for less than 24 hours as classified per ISO 10993-1:2018, the material supplier must provide documentation addressing cytotoxicity per ISO 10993-5 and sensitization per ISO 10993-10. Sintered PBT01 requires verification that no polyester thermal degradation by-products remain after post-processing. Isopropyl alcohol wash of 99.9% purity for 10 minutes followed by deionized water rinse at 40 kHz ultrasonic frequency removes detectable surface monomers. Residual organic compounds measured by headspace gas chromatography per ASTM D4526 remain below 0.1 µg/cm². Sterilization compatibility is a critical boundary condition. Gamma sterilization at 25 kGy to 40 kGy per ISO 11137-1 causes measurable tensile strength reduction of 5% to 8% when tested per ISO 527-2 Type 1BA specimens. Ethylene oxide sterilization per ISO 11135 leaves residual EtO levels below 1 ppm after 48 hours aeration at 40 °C. Steam autoclave sterilization at 121 °C for 20 minutes is prohibited for as-sintered PBT01. Hydrolysis of ester linkages accelerates above 110 °C in saturated steam. This results in molecular weight reduction and embrittlement. Sintered medical device housings must not be used for implantable applications or for surfaces contacting mucosal tissue or breached skin. This limitation is absolute. Production batches require lot-level documentation. Intrinsic viscosity measured per ISO 1628-1 must remain within 3% of the virgin powder reference value. Melt volume flow rate measured per ISO 1133-1 at 250 °C with 2.16 kg load must not deviate by more than 10% from virgin powder. These process control parameters serve as gate release criteria for medical device manufacturing. Published data for this specific PBT01 configuration in ISO 10993-5 testing is limited. Verification testing on each finished powder batch is therefore mandatory before release to medical device customers.
Repeatedly subjected to engagement-disengagement cycles exceeding 5,000 events per season, cyclocross cleat bodies require predictable flexural stiffness at the pedal retention interface. Sintered PBT01 cleat prototypes at 100 µm layer thickness maintain engagement groove tolerance of 2 mm ± 0.1 mm. Wear volume loss against chromoly steel measured per ASTM G133 is approximately 0.5 mm³ per km at 10 N contact load. This corresponds to a service life of 2,000 km to 3,000 km before groove geometry falls below functional tolerance. Each part requires glass bead blasting at 0.4 MPa with 100 µm to 150 µm spheres followed by 10× magnification inspection. Voids larger than 0.5 mm within 2 mm of the engagement surface reject the part per production inspection protocol. Build orientation places the engagement groove perpendicular to layer stacking. This orientation maximizes interlayer shear strength on the wearing surface.
Before any PBT01 component can be installed in a pressurized aircraft cabin with 19 or more passenger seats, the sintered part must demonstrate compliance with FAR 25.853(a) vertical burn testing per Appendix F Part I. Unfilled injection-molded PBT achieves UL 94 V-0 only with halogenated or phosphorus-based flame retardant additives. The base PBT01 powder is an unfilled material. Publication of vertical burn test data for unfilled sintered PBT01 under FAR 25.853(a) is limited. This means compliance for aircraft interior brackets and clips requires verification testing on every powder batch. Test specimens of 305 mm × 75 mm × 3 mm are sintered at 120 µm layer thickness. Test methodology per FAR 25.853 Appendix F Part I imposes a 60-second maximum afterflame time, a 30-second maximum drip flame time, and a burn length not exceeding 152 mm. Unfilled PBT without flame retardant additives typically fails these criteria. Afterflame times of unfilled PBT exceed 60 seconds. This is a critical processing boundary. Aircraft interior components produced from PBT01 must either be limited to installations not requiring FAR 25.853 testing or be post-processed with a flame retardant coating system. Coatings qualified for this purpose include intumescent epoxy systems with documented compliance verification. Post-process coating adds 0.2 mm to 0.4 mm to external dimensions. Assembly drawings must account for this additional thickness on mating surfaces. The coating must be validated for adhesion per ASTM D3359 Method B. Tape pull testing must achieve a rating of 4B or higher. Non-cabin installations such as avionics rack spacers in unpressurized areas may not require FAR 25.853 compliance. Each application must be reviewed by the cognizant airworthiness authority. Production-scale experience on EOS P396 systems has demonstrated that unfilled PBT01 sintered parts maintain dimensional stability during 1,000 hours at 85 °C and 85% relative humidity with dimensional change of less than 0.3%. This property supports applications in avionics bay environments where hydrocarbon exposure is absent. Unfilled PBT01 is not qualified for seating components, class dividers, or overhead bin structures where heat release rate testing per FAR 25.853(d) is mandatory. The oxygen index of unfilled PBT measured per ISO 4589-2 is approximately 20% to 22%. Materials with oxygen index below 28% are generally considered flammable in 28% oxygen-enriched atmospheres.
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Mitsubishi Chemical ROLASERIT PBT01 is an unfilled polybutylene terephthalate powder formulated for laser powder bed fusion systems using 10.6 µm CO₂ laser sources and actively heated build chambers. The polymer is a semi-crystalline polyester based on 1,4-butanediol and terephthalic acid or dimethyl terephthalate; the aromatic terephthalate segment in the repeating unit raises melt temperature, stiffness, and solvent resistance relative to aliphatic polyamides. The PBT01 designation identifies a laser-sintering grade rather than an injection-moulding pellet, meaning that particle size distribution, melt viscosity, and crystallization behaviour are controlled for recoating and layer consolidation. Product-specific values are supplied in the manufacturer’s certificate of analysis and current datasheet; independent third-party datasets for PBT01 remain limited.
From a molecular perspective, the governing process issue is the narrow temperature interval between PBT melt onset and recrystallization. PBT01 is not a drop-in replacement for PA12 in every powder bed system. Build chamber design, thermal imaging, and feedstock drying must be qualified together because the higher bed temperature and oxygen sensitivity of PBT place greater demand on process control than standard polyamide 12 powders.
Unfilled PBT has a higher melting endotherm than PA12. Typical differential scanning calorimetry values place PBT melting between 220 °C and 225 °C, whereas PA12 generally melts between 176 °C and 180 °C. This difference shifts the powder bed build chamber to a higher setpoint and increases thermal stress on the powder cake. The higher density of PBT, approximately 1.30–1.32 g/cm³ compared with 1.00–1.03 g/cm³ for PA12, also changes part mass and powder bed loading. Tensile and flexural moduli are higher for unfilled PBT; tensile modulus is typically 2.4–2.7 GPa and flexural modulus 2.2–2.6 GPa, while PA12 values are usually 1.4–1.8 GPa and 1.2–1.6 GPa respectively. Conversely, unfilled PBT has lower notched impact strength than PA12, particularly below 0 °C, so impact-dominated parts require explicit evaluation.
| Property | Unfilled PBT powder range | PA12 powder reference range | Test method |
|---|---|---|---|
| Melting endotherm peak | 220–225 °C | 176–180 °C | ISO 11357-3:2018 |
| Density | 1.30–1.32 g/cm³ | 1.00–1.03 g/cm³ | ISO 1183-1:2019 |
| Tensile modulus | 2.4–2.7 GPa | 1.4–1.8 GPa | ISO 527-2:2012 |
| Flexural modulus | 2.2–2.6 GPa | 1.2–1.6 GPa | ISO 178:2019 |
| Heat deflection temperature at 1.82 MPa | 50–60 °C | 45–55 °C | ISO 75-2:2013 |
| Equilibrium moisture at 23 °C/50 % RH | 0.2–0.3 % | 0.7–1.0 % | ISO 62:2008 |
Values in the table are generic screening data for unfilled polybutylene terephthalate and polyamide 12 powder feedstocks. They are not a substitute for the current PBT01 datasheet, because additive formulation, molecular weight, and powder morphology can shift measured values.
PA11 typically provides higher ductility and impact resistance than PA12 and is often selected for snap-fit parts; PBT01 cannot be assumed to match that behaviour. The advantage of PBT01 over PA11 and PA12 appears in applications where low moisture uptake, higher flexural modulus, and solvent resistance outweigh the penalty of higher density and narrower processing latitude. However, PA12 and PA11 powders have more extensive production-proven reuse cycles; PBT01 users should plan for more frequent powder qualification because published data for this specific configuration are limited.
In an actively heated powder bed fusion chamber, the bed temperature is maintained between the melt onset and recrystallization. For unfilled PBT, the working interval can be as narrow as 10–15 °C; stable production requires closed-loop infrared or thermocouple feedback and uniform gas flow. If the bed temperature falls below the recrystallization onset, accumulated layers curl and the recoater blade can strike the part. If the bed temperature approaches the melt peak, powder caking increases, part definition decreases, and breakout becomes difficult. Thermal mapping across a 300 mm build platform in production-scale machines can show edge-to-centre offsets above ±3 °C; this offset is sufficient to narrow an already small process window.
Laser energy input for PBT must balance interlayer fusion against melt-pool oxidation and thermal degradation. The 10.6 µm CO₂ wavelength is absorbed by polyester, but the exact energy density must be determined on the target machine. Layer thickness is commonly set between 0.10 mm and 0.12 mm for semi-crystalline powders; fine features may require thinner layers, reduced scan spacing, and lower scan speed. The chamber oxygen concentration should be held below 1.0 % by volume using dry nitrogen, and the gas dew point should be maintained below -40 °C. These conditions reduce thermo-oxidative discoloration and suppress porosity caused by moisture release.
Recrystallization kinetics dominate part quality. PBT can crystallize rapidly, and the non-isothermal recrystallization temperature is close to the melt onset. Operators should monitor the temperature difference between melting peak and recrystallization peak on each powder lot by ISO 11357-3:2018. A reduction in this difference, or a broadening of the melting endotherm, indicates contamination, ageing, or molecular weight change. Lot changes should trigger a new single-layer exposure test and dimensional verification because published data for PBT01-specific parameter sets are limited.
Although PBT absorbs less equilibrium moisture than PA12, residual water above 0.02 % by Karl Fischer titration can generate porosity and hydrolysis in the melt state. Production-scale handling of PBT powders in open feed hoppers exposed to relative humidity above 60 % has been associated with electrostatic clumping and flow variation. Before loading, powder should be sieved through a 150 µm mesh and dried at 80–100 °C under dehumidified air until moisture is below 0.02 %. Drying time depends on the residual moisture load and dryer dew point; vacuum drying may be used if the powder has been stored in humid conditions.
Recycled powder from the build chamber has multiple thermal histories. Molecular weight can shift through hydrolysis, thermo-oxidative chain scission, or post-condensation. A practical refresh regime for many unfilled PBT laser-sintering powders uses 30–50 wt% virgin powder, but the exact PBT01 ratio requires evaluation of melt volume-flow rate according to ISO 1133-1:2022, powder flow according to ISO 6186:2019, and bulk density according to ISO 60:1977. A Hausner ratio below 1.25 is a typical acceptance criterion for free-flowing powder bed fusion feedstocks; values above this threshold suggest particle shape change, fines generation, or moisture uptake.
Particle size distribution should be tracked by laser diffraction per ISO 13320-1:2020. Typical powder bed fusion feedstocks have a D50 between 40 µm and 70 µm, a D10 above 20 µm, and a D90 below 110 µm. PBT01 lot-specific limits must be read from the certificate of analysis, because off-spec fines can increase electrostatic adhesion and reduce recoater uniformity.
Storage conditions also affect lot-to-lot consistency. Powder containers should be kept sealed at 15–30 °C and below 50 % relative humidity. Opened containers should be resealed under dry nitrogen or dehumidified air; extended exposure to humid ambient air can increase moisture to levels that cannot be fully corrected by a short drying cycle if the powder has already begun to hydrolyse.
After sintering, PBT01 parts should be allowed to cool inside the powder cake to a temperature below the recrystallization point before extraction. Slow cooling promotes dimensional stability in thin walls; fast removal can increase warpage and residual stress. Blasting with glass or ceramic media can remove sintered surface powder, but aggressive bead blasting may reduce surface gloss and alter critical dimensions. Unlike PA12, unfilled PBT has limited dye uptake in aqueous dye baths; colour matching usually requires pre-coloured powder or a coating rather than post-dyeing. The machinability of PBT01 parts is acceptable for drilling and tapping, but the lower notched impact strength relative to PA12 means that threaded holes in edge zones should include chamfers and generous wall thicknesses.
Equipment compatibility extends to recoater blade material. If PBT01 lots contain high fines, the powder can be mildly abrasive; hardened steel or ceramic-coated recoaters reduce scoring and maintain uniform layer thickness. Vacuum extraction during cleaning should use grounded hoses because polyester powders can accumulate static charge. Filtration systems with high-efficiency particulate air filters should be used to contain fines during breakout and sieving operations.
Because unfilled PBT offers low equilibrium moisture, stable dielectric properties, and resistance to automotive fuels, oils, and weak acids, it is considered for connector housings, sensor brackets, and rigid underhood covers where PA12 may be too flexible or too moisture-sensitive. Electrical property screening should include comparative tracking index per IEC 60112:2020 and dielectric strength per IEC 60243-1:2013. Unfilled PBT can often achieve a comparative tracking index above 400 V, but the exact value depends on additives and printing conditions.
Continuous exposure to hot water above 60 °C or to strong alkaline solutions is not recommended because ester hydrolysis accelerates under these conditions. The printed part must also be considered anisotropic: tensile and flexural values in the Z orientation are typically lower than in the XY orientation, so load-bearing parts should be qualified in all three build orientations. For elevated-temperature dimensional stability, heat deflection temperature per ISO 75-2:2013 and coefficient of linear thermal expansion per ISO 11359-2:2021 should be measured on printed specimens, not on injection-moulded plaques.
Comparative selection between PBT01 and PA12 should include dynamic mechanical analysis per ISO 6721-1:2019 if the service temperature approaches the glass transition. Unfilled PBT has a glass transition temperature in the 45–60 °C range; PA12 also loses stiffness above its glass transition, so the final choice must be based on measured part performance rather than resin datasheet values alone. Creep and fatigue data for laser-sintered PBT01 remain limited, so safety-critical or long-duration structural parts require additional validation.
Regulatory status and safety information must be obtained from the current safety data sheet. Unfilled polybutylene terephthalate is not automatically compliant with food-contact or medical-grade requirements, and any application requiring FDA 21 CFR clearance must be verified on the specific printed part, not assumed from resin type. Electrical and electronic applications may require RoHS compliance evidence from the manufacturer; PBT01-specific documentation should be requested.
Incoming powder lots should be inspected for particle size distribution, residual moisture, and melt volume-flow rate before qualification builds. A production qualification should include tensile specimens per ISO 527-2:2012, flexural specimens per ISO 178:2019, and density by displacement per ISO 1183-1:2019. Because laser-sintered mechanical properties are anisotropic, specimens should be printed in XY, XZ, and Z orientations. Process changes in laser power, scan strategy, chamber heating, or powder refresh ratio require re-qualification. Published data for PBT01-specific builds are limited; each machine and powder lot should be verified independently before production release.