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Powder metallurgy for dental biomaterials: Applications, processing, properties and clinical relevance

dc.contributor.authorMoghanian, Amirhossein
dc.contributor.authorSafaee, Sirus
dc.contributor.authorKizilkurtlu, Ahmet Akif
dc.contributor.authorMehrdar, Mohammad
dc.contributor.authorFarmani, Ramin
dc.contributor.authorMehrani, Soroush
dc.contributor.authorAkpek, Ali
dc.contributor.authorNesabi, Mahdis
dc.date.accessioned2026-06-27T15:33:03Z
dc.date.issued2026
dc.description.abstractAdvances in powder metallurgy (PM) have revolutionized the fabrication of dental biomaterials by enabling precise microstructural control and tailored porosity (up to 80 % porosity in scaffolds) while simultaneously reducing waste and processing time. Although conventional PM processes offer a versatile toolkit for dental applications, consolidation techniques achieve near-full densification (exceeding 85 % of theoretical density) and refine microstructures in metallic and ceramic dental restoratives, resulting in enhanced mechanical integrity (compressive strength up to 203 MPa for TiB2/Ti composites) and biocompatibility. Post-processing treatments, ranging from thermal unbinding and sintering schedules to surface modifications, further optimize the mechanical performance (Young's modulus matching bone at 2.2-12.1 GPa), surface finish, and corrosion resistance of the PM-derived dental components. A diverse array of biomaterials, including titanium-indium alloys for endodontic posts and cobalt-chromium partial denture frameworks, has been successfully produced via PM, demonstrating favorable osseointegration and mechanical performance (tensile strength up to 290 MPa for Ta-Zr alloys). Comprehensive performance evaluations, including fatigue testing, wear analysis, and cytocompatibility assays, confirm the clinical viability of PM-fabricated dental biomaterials. Comparative analyses further elucidate the trade-offs between process parameters, part complexity, and cost efficiency, thereby guiding rational selection for specific prosthetic applications. Nonetheless, challenges persist in scaling PM processes for custom dental geometries, managing the residual porosity (5-15 % in sintered parts), and ensuring consistent biocompatibility across diverse alloy systems. This review aims to cover and analyze these issues by mentioning recent advancements, current limitations, and the future landscape of dental PM-derived biomaterial fabrication in a wide framework.en
dc.description.urihttps://doi.org/10.1016/j.jnoncrysol.2025.123921
dc.identifier.doi10.1016/j.jnoncrysol.2025.123921
dc.identifier.eissn1873-4812
dc.identifier.issn0022-3093
dc.identifier.urihttps://hdl.handle.net/20.500.14981/71832
dc.identifier.volume674
dc.identifier.wos001648705100001
dc.language.isoeng
dc.publisherELSEVIER
dc.relation.ispartofJOURNAL OF NON-CRYSTALLINE SOLIDS
dc.subjectPowder metallurgy
dc.subjectDental biomaterial
dc.subjectNano-composite
dc.subjectBio fabrication
dc.subjectAdditive manufacturing
dc.subjectSOL-GEL METHOD
dc.subjectMECHANICAL-PROPERTIES
dc.subjectHYDROXYAPATITE COMPOSITES
dc.subjectTITANIUM
dc.subjectIMPLANTS
dc.subjectALLOYS
dc.subjectMICROSTRUCTURE
dc.subjectDENSIFICATION
dc.subjectFABRICATION
dc.subjectCOATINGS
dc.subjectMaterials Science
dc.titlePowder metallurgy for dental biomaterials: Applications, processing, properties and clinical relevance
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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