| HS Code | 664030 |
| Density | 1.12 g/cm³ |
| Viscosity | 250 cP at 30°C |
| Critical Exposure | 12.7 mJ/cm² |
| Penetration Depth | 0.14 mm |
| Tensile Strength | 55 MPa |
| Tensile Modulus | 2.70 GPa |
| Elongation At Break | 10% |
| Flexural Strength | 85 MPa |
| Flexural Modulus | 2.60 GPa |
| Hardness | 85 Shore D |
| Glass Transition Temperature | 80°C |
| Water Absorption | 0.30% |
| Impact Strength | 0.50 J/cm |
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DSM Somos ProtoGen™ 18920 Liquid Photopolymer, UV Postcure is formulated for 355 nm laser-scanned stereolithography platforms in which parts are built layer-by-layer and subsequently stabilized by ultraviolet postcure. The grade belongs to the Somos ProtoGen family, which is commonly positioned for polypropylene-like functional prototypes and master patterns requiring dimensional repeatability after secondary processing. In production-scale operations, the resin is processed at a vat temperature of 30 °C ± 2 °C, with layer thickness selections of 0.050 mm, 0.100 mm, or 0.150 mm depending on feature size, surface-finish constraints, and vertical accuracy. Machines using galvanometer-controlled scanning and a nominal wavelength of 355 nm, typified by the 3D Systems Viper si2 and larger-frame SLA 5000 series, are common reference platforms. The material must be shielded from ambient UV sources; storage in the original sealed container at 15 °C to 30 °C is generally required to preserve polymerization response and prevent premature gelation.
Lot-to-lot repeatability in the ProtoGen 18920 vat begins with storage and fluid handling, not only with machine parameter sets. Resin stored below 15 °C may develop viscosity stratification and should be brought to 30 °C ± 2 °C without direct heating or open-flame sources. Depending on container volume, passive equilibration can require 2 h to 4 h; forced-air heaters are not recommended because localized skin heating may initiate dark polymerization at the container wall. Containers exposed to high-humidity environments should be kept sealed when not in use. Absorption of atmospheric moisture can shift the critical exposure dose and produce a tacky or powdery surface on the first layers after build startup. Gentle mixing is acceptable only if it does not generate bubbles; high-shear mixing can entrain air that appears as microvoids after recoating. Production sites operating in relative humidity above 60 % should evaluate predrying or dry-air purging of the resin handling area before the build is released.
Depth of polymerization in this resin is a function of the working-plane exposure energy rather than the programmed slice thickness alone. When the measured scan spacing exceeds the 1/e² beam width by more than 15 %, adjacent laser scan tracks may fail to form a continuous overlap, producing weak interlayer planes that are not visually obvious in the green part. Real-world solid-state SLA platforms with nominal laser output between 400 mW and 800 mW frequently deliver only 35 % to 60 % of nominal output at the vat surface after optics attenuation and quartz-window fouling. Periodic calibration with a 355 nm thermopile radiometer is therefore necessary before critical builds. Drift beyond 5 % from the baseline power measured at the last successful run is a standard trigger for inspecting the beam expander, galvo mirrors, and vat window before proceeding. These observations reflect production-scale SLA equipment behavior because machine configuration strongly affects the actual exposure dose delivered to the resin.
Recoat uniformity in the ProtoGen 18920 vat is determined primarily by the viscosity of the liquid resin at the build temperature and by the geometry of the recoater blade. If the resin temperature falls below 28 °C, viscosity rises enough to slow leveling after each recoater pass; blade skip marks and trapped air can then appear on the top build layer. On fixed-gap recoater systems using a 0.254 mm blade gap, the affected area may show a surface depression whose depth corresponds to the uncured resin that was not correctly displaced. If the vat temperature exceeds 32 °C, the induction time for dark polymerization shortens, allowing gel particles to form in stagnant regions of the vat. These particles can adhere to the part surface or create raised defects after multiple sequential builds. The industrial control window of 30 °C ± 2 °C is therefore not a convenience value; it balances viscosity reduction against the onset of premature polymerization in the vat.
On production-scale systems, recoat speed is generally set between 80 mm/s and 140 mm/s for large-area recoating. Blade acceleration is ramped so that the liquid meniscus behind the blade does not break and entrain air; a broken meniscus can generate voids whose lateral width exceeds 0.1 mm and whose location follows the recoater trailing edge. The optimum speed depends on resin lot viscosity, vat temperature, and recoater design. Operators should log the viscosity of each incoming lot at 30 °C using a rotational viscometer method such as ASTM D2196-20 or a cone-and-plate technique aligned to ISO 2884-2:2006. A lot-to-lot viscosity shift of more than 10 % relative to the preceding lot is a valid cause for recoat parameter adjustment, even if the resin remains within the supplier’s acceptance range.
When the green part is removed from the build platform, the photopolymer network remains intentionally underconverted; this preserves part ductility during support removal but leaves reactive groups that must be consumed during UV postcure. Excess liquid resin is first removed by sequential solvent cleaning. A primary bath of isopropyl alcohol with concentration above 90 % is common, followed by a second clean bath to avoid redeposition of diluted resin. Compressed-air drying at 2 bar to 4 bar removes solvent from recesses; air lines must be filtered to avoid oil contamination. A tacky residue after drying indicates that the solvent bath is saturated or that the part was not fully drained. If tripropylene glycol monomethyl ether is used as an alternative, the vented cleaning station must be configured for its lower vapor pressure and longer evaporation time.
UV postcure chambers for this product class typically use metal-halide or high-pressure mercury lamps with emission between 320 nm and 420 nm. Parts are placed on rotating or indexing trays to distribute exposure across all surfaces. Total UV dose measured in the UV-A band is usually held at 20 J/cm² to 40 J/cm² per exposed face. Doses below 15 J/cm² can leave heat deflection temperature and solvent resistance below the fully cured baseline; doses above 60 J/cm² can embrittle thin-wall areas and increase oxidation-driven yellowing. Postcure is exothermic, and thin-wall sections below 1.0 mm may warp when placed on dark metal trays that absorb incident energy and create thermal gradients. Sustained part-surface temperatures above 60 °C during UV postcure are generally outside the intended window for dimensionally stable patterns. Radiometer calibration should be performed against a UV source of known spectral output; lamp-hour counters alone do not verify that the correct dose reached the part surface.
Mechanical properties reported for DSM Somos ProtoGen™ 18920 must be interpreted according to specimen geometry, build orientation, postcure schedule, and conditioning environment. Producers of SLA photopolymer data typically follow the matrix shown in Table 1. The use of a single set of parameters without reporting build orientation can understate anisotropy and mislead comparisons with large-format industrial resins.
| Property | Standard/Method | Specimen/Condition | Unit |
|---|---|---|---|
| Tensile strength, elongation | ASTM D638-14 / ISO 527-2:2012 | Type I / 1B, crosshead 5 mm/min, 23 °C ± 2 °C, 50 % ± 5 % RH | MPa, % |
| Flexural modulus | ASTM D790-17 / ISO 178:2019 | Three-point bend, span 64 mm, crosshead 1.3 mm/min | MPa |
| Heat deflection temperature | ASTM D648-16 / ISO 75-2:2013 | Edgewise at 0.45 MPa, heating rate 2 °C/min | °C |
| Notched Izod impact | ASTM D256-10 / ISO 180:2019 | Method A, notch radius 0.25 mm, 23 °C ± 2 °C | J/m, kJ/m² |
| Water absorption | ASTM D570-98 | 24 h immersion, 23 °C | % |
| Hardness | ASTM D2240-15 | Shore D, 3 s reading | Shore D |
Published numerical values for ProtoGen 18920 are not reproduced here because open-source summaries often lag behind formulation revisions and may omit orientation-specific data. The supplier’s current technical datasheet remains the authoritative source for absolute property boundaries; the matrix above is supplied only to define the test conditions under which such values should be compared.
A deficient postcure cycle may not be apparent from Shore hardness measurements alone. Parts can appear solid but retain an underconverted core or interlayer region that fails under service conditions well below expected tensile stress. In many SLA photopolymers, an undercured interlayer is most clearly observed as an increase in the ratio of horizontal to vertical tensile strength; anisotropy ratios above 1.5 have been documented in production audits when the postcure dose was below the critical threshold. Isopropyl alcohol wipe testing can identify residual liquid or lightly crosslinked resin on the surface, but it does not quantify conversion depth. Dynamic mechanical analysis on fully cured and deliberately undercured specimens indicates that storage modulus at 50 °C may be lower by 20 % or more when UV radiometer calibration has drifted by 10 %. This modulus deficit is not recoverable by subsequent solvent cleaning or surface priming.
Load-bearing applications expose underconverted interlayer regions that routine Shore hardness measurements miss. The first visible sign is often a whitening or delamination at support-scar locations after the part is subjected to bending or impact. Because the UV postcure step is intended to increase crosslink density through the full wall thickness, a short or shadowed postcure cycle leaves the core softer than the surface. On thick sections above 6 mm, postcure uniformity is particularly sensitive to tray placement and part orientation; underside surfaces facing the tray may receive less than 50 % of the incident dose unless parts are rotated. Production facilities that rely on dynamic mechanical analysis or differential scanning calorimetry use those techniques to verify that the glass transition or storage-modulus baselines are reached before releasing functional prototypes. A single bulk property value is insufficient for process verification because residual underconversion can be localized in the interlayer region.
Process calibration for scanning-laser SLA platforms is summarized in Table 2. The tolerances listed are industrial control limits, not absolute resin property limits; they provide a starting point for process-stability assessment on UV-laser machines.
| Variable | Typical Industrial Tolerance | Observation Method |
|---|---|---|
| Vat temperature | 30 °C ± 2 °C | Calibrated thermocouple at vat perimeter |
| Laser power at vat surface | ±5 % of baseline | 355 nm radiometer |
| Recoat speed | 80 mm/s–140 mm/s | Machine parameter verification |
| UV postcure dose | 20 J/cm²–40 J/cm² per face | UV radiometer, 320 nm–420 nm band |
| Recoat blade gap | 0.254 mm nominal | Feeler gauge before build |
Typical production uses for DSM Somos ProtoGen™ 18920 include vacuum-casting master patterns, short-run enclosures, snap-fit demonstration parts, form-and-fit verification housings, and airflow-test components in which moderate dimensional stability after secondary processing is required. The grade is selected over lower-temperature general-purpose SLA resins when the part will undergo silicone molding, painting, or thermal forming of subsequent casting materials. However, users should not substitute ProtoGen 18920 data for ProtoGen 18120 or ProtoGen 18420 data without reviewing the current datasheet; the suffix designations correspond to different property balances, and open-source cross-comparisons frequently understate orientation and postcure effects. Published data for this specific configuration is limited for sustained load at temperatures above 75 °C and for long-term outdoor weathering; those applications require application-specific testing rather than direct datasheet transfer. The material should not be assumed to comply with FDA 21 CFR food-contact requirements, ISO 10993 biocompatibility requirements, or REACH/RoHS restrictions without current supplier documentation. Strong alkaline cleaning solutions above 50 °C and prolonged immersion in aggressive organic solvents should be treated as incompatibilities unless comparative chemical resistance data is supplied. Before silicone tooling compounds are used against the resin pattern, the specific platinum-catalyzed silicone should be tested for cure inhibition because partially postcured photopolymer residues at the surface can interfere with the silicone crosslinking reaction at the interface.