Ti-6Al-4V ELI (Grade 23)
metaltitanium alloy — alpha-beta (extra low interstitial)
Composition — UNS R56401 / ASTM F3001-14 / ASTM F136
| Element | Min % | Max % | Notes |
|---|---|---|---|
| Ti | bal. | balance | |
| Al | 5.50 | 6.500 | Alpha stabiliser; narrows range vs. Grade 5 (5.5–6.75) for tighter microstructure control |
| V | 3.50 | 4.500 | |
| Fe | — | 0.250 | Reduced from 0.30% (Grade 5) — Fe is a beta stabiliser that affects transformation behaviour |
| O | — | 0.130 | Key interstitial — primary driver of ductility and fracture toughness improvement vs. Grade 5. Oxygen strengthens but embrittles; ELI reduces O limit from 0.20% to 0.13%. |
| N | — | 0.030 | Reduced from 0.05% (Grade 5) |
| C | — | 0.080 | |
| H | — | 0.012 | Slightly lower H limit than Grade 5 (0.015%) — hydrogen embrittlement is a concern in implant environments (in vivo) |
| Y | — | 0.005 |
Mechanical & thermal properties — 4 conditions
| Property | LPBF as-built (XY) | LPBF annealed (700–800°C / 2h / AC) (XY) | LPBF + HIP (920°C / 100 MPa / 2h) | EBM as-built |
|---|---|---|---|---|
| Elastic modulus | 105–120 GPa | — | — | — |
| Yield strength (0.2%) | 930–1120 MPa | 759–1000 MPa | 780–930 MPa | 760–920 MPa |
| Ultimate tensile strength | 1050–1280 MPa | 860–1050 MPa | 860–1010 MPa | 860–1000 MPa |
| Elongation at break | 5.0–13.0 % | 10.0–20.0 % | 13.0–24.0 % | 12.0–21.0 % |
| Hardness (HV) | — | 295–355 HV10 | — | — |
| Fatigue strength | — | 480–680 MPa | 620–820 MPa | — |
| Fracture toughness KIC | — | 60.0–95.0 MPa√m | 72.0–110.0 MPa√m | — |
| Density | 4.43 g/cm³ | — | — | 4.43 g/cm³ |
| Relative density | 99.0–100.0 % | — | — | — |
| Thermal conductivity | 6.7 W/m·K | — | — | — |
| CTE | 8.4–9.0 µm/m·K | — | — | — |
| As-built surface Ra | — | — | — | 20.0–45.0 µm |
Values shown as min–max where a spread is reported, otherwise as typical ± unit. Ranges reflect inter-source variation, not single-sample scatter. All values are for AM-processed specimens unless noted.
Engineering considerations
- Implant qualification pathway (US): ASTM F3001 for powder and part properties, FDA AM Guidance 2017 for 510(k)/PMA submission. Device-level testing (ISO 7206 for hip, ASTM F3141 for spine, ISO 14801 for dental) is required regardless of material compliance.
- EBM for orthopaedics: lattice design for osseointegration should target pore size 300–600 µm and porosity 50–70% — these values are empirically proven for bone ingrowth. EBM Arcam A2XX series is the dominant platform for orthopaedic Ti-6Al-4V ELI.
- LPBF for medical: stress relief (600°C/2h in vacuum) plus solution anneal (730–800°C/2h, furnace cool) is the standard post-processing route for LPBF ELI implants. HIP (920°C/100 MPa/2h) adds cost but is justified for fracture-critical spinal implants.
- Anisotropy consideration: for spinal cages loaded in axial compression (primary load), the Z-direction (lowest LPBF strength) is aligned with the loading axis — design for worst-case Z-direction properties unless post-HT restores isotropy.
- Wear surfaces: Ti-6Al-4V ELI is unsuitable as a bearing surface without modification. For modular neck tapers and femoral head interfaces, specify: (a) PVD TiN coating (HV 2000, Ra < 0.1 µm), (b) anodised TiO₂ (corrosion protection), or (c) mate with UHMWPE, CoCrMo ceramic, or alumina.
- Sterilisation compatibility: steam autoclave (134°C, compatible), gamma irradiation (25 kGy, compatible), EtO (compatible). Select final finish before sterilisation — passivation per ASTM F86 recommended before gamma or EtO sterilisation.
- Osseointegration surface design: as-built EBM surfaces (Ra 20–35 µm) provide excellent primary fixation. Further roughening via grit blasting or acid etching is used when Ra > 35 µm osseointegration texture is desired. Do not polish osseointegration surfaces.
- Regulatory note: EU MDR 2017/745 Class III (implantable devices) requires Notified Body involvement. Clinical evaluation and post-market follow-up are mandatory in addition to material and device testing.
Advantages
- Biocompatible — ASTM F136 / ISO 5832-3 certified; no cytotoxicity, genotoxicity, or immunogenicity concerns for long-term implantation
- Superior fracture toughness vs. Grade 5 — KIC ~80–90 MPa√m vs. ~55–70 MPa√m — critical for fracture-critical implants
- Better fatigue crack growth resistance — lower crack propagation rate in body fluid environment vs. Grade 5
- Meets ASTM F3001 property minimums as-built after EBM — simplifies implant qualification pathway
- EBM enables porous osseointegration structures and solid regions in a single build — no assembly
- Elastic modulus (110–115 GPa) closer to cortical bone (10–30 GPa) vs. cobalt chrome (200 GPa) — reduces stress shielding
- Excellent corrosion resistance in body fluids — passive TiO₂ film is stable in saline, pH 5–9, and plasma
Limitations
- Lower yield and UTS than Grade 5 — ~10% less strength due to lower O content. Acceptable for most implant designs but requires awareness in structural analysis
- LPBF as-built elongation (5–8%) insufficient for implant standards — annealing mandatory for LPBF medical applications
- Poor wear resistance — Ti alloys are not suitable for bearing surfaces without coating (TiN, TiO₂) or ceramic insert
- Extremely high cost — ELI grade powder is typically 20–40% more expensive than Grade 5 powder
- EBM surface roughness (Ra 20–45 µm) — bearing surfaces require machining to Ra < 0.1 µm; adds cost and setup complexity
- Titanium is MRI compatible but causes imaging artefacts — plan implant orientation to minimise diagnostic shadow
- No published AM ELI fatigue endurance standard — each implant design requires device-level fatigue testing to ISO 7206, ASTM F1800, or equivalent
- Powder handling: same ATEX/OSHA requirements as Grade 5; ELI powder must be handled in inert atmosphere due to fine particle reactivity
Typical applications
Industries
Standards & certifications
Ti-6Al-4V ELI parts produced by powder bed fusion (LPBF and EBM) — defines composition, powder, and minimum mechanical property requirements for the ELI grade
The primary AM standard for ELI grade. Mechanical property minimums are equivalent to wrought ASTM F136 — this enables AM implant qualification using the same acceptance criteria as wrought.
Grade 5 Ti-6Al-4V — referenced for comparison; ELI grade (F3001) has lower property minimums due to reduced interstitial content
Wrought Ti-6Al-4V reference standard for implant property comparison
Wrought ELI reference. AM ELI implants must also satisfy FDA AM Guidance 2017 (US) or EU MDR Annex II (Europe).
Medical device quality management system — required for implant manufacturers
Biocompatibility evaluation framework — required for all implantable AM devices
FDA guidance for AM medical devices — submission requirements for 510(k) and PMA
Compatible AM processes (2)
Other metal materials
Related calculators
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