Metals, Ceramics, Glasses, and Glass-Ceramics Flashcards

1
Q

Common Alloys..

A
  • classified by American Society for Testing and Materials (ASTM)
  • Ti alloys, Co-Cr alloys, Stainless Steel
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2
Q

Titanium Alloys

A
  • Commercially pure Ti with some oxygen, aluminum, and vanadium
  • Two most common: CP (commercially pure) and extra-low interstitial (ELI)
  • in ELI, aluminum is alpha phase stabilizer, while vanadium is a beta phase stabilizer
  • addition of O, C, and N interstitially in both alloys strengthens the metal, making deformation more difficult (impeding dislocation motion)
  • superior corrosion resistance, bioinert (minimal fibrous capsule), less stress shielding due to similar elastic modulus to bone
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3
Q

Nitinol

A
  • equally nickel and titanium alloy with shape memory properties
  • two different temp-dependent crystal structures (martensite in low temp, austenite in high temp), in different phases the material has different properties
  • nickel is allergenic at high concentrations, can use titanium oxide layer as a barrier
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4
Q

Stainless Steel

A
  • Iron and carbon alloy with impurities
  • chromium, nickel, Mo, some N, Mg, P, and C added
  • 316L is widely implanted (0.03% max carbon, prevents chromium carbide formation which would reduce oxide layer and decrease corrosion resistance)
  • properties are customizable through processing like coldworking or annealing
  • all have face centered cubic structure that is non-magnetic
  • adding in larger atoms in alloys leads to distortions in crystal structure (grain boundary irregularities), but smaller atoms in interstitial spaces prevents dislocations
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5
Q

Cobalt-Chromium alloys

A
  • F75 alloy is popular (mostly Co, less Cr)
  • very corrosion resistant
  • add tungsten or molybdenum, since they’re larger atoms can impede dislocation motion
  • Co absorb stress in phase transformation, leading to excellent wear resistance
  • hard to fabricate to shape (in alpha phase can form large grain sizes)
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6
Q

Type 1 Bioceramics

A
  • dense, nonporous, almost inert (no biological bonding at tissue interface)
  • morphological fixation
  • implanted via compression loading (movement can wear particles and lead to formation of fibrous capsule)
  • ex: alumina (biocompatible, fine grain size, high wear resistance, strength/hardness, can cause stress shielding in older patients)
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7
Q

Type 2 Bioceramics

A
  • nearly inert, microporous, rely on ingrowth of tissues into the pores on the surface or throughout the implant
  • biological fixation
  • pore size must exceed 100 microns for proper ingrowth of tissue
  • used for non-loading (porosity reduces the mechanical strength)
  • interconnects pores or coats porous metals (derived from hydroxyapatite, or converted from coral or animal bone)
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8
Q

Type 3 Bioceramics

A
  • elicit a biological response at the interface, forming interfacial bond between the tissue and material
  • bioactive fixation (‘binds’ to bone, sometimes soft tissue)
  • examples: non-porous hydroxyapatite and composites, bioactive glasses and glass-ceramics
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9
Q

Types 3A-3D Bioceramics

A
  • vary in concentrations of silicon, sodium, calcium, and phosphorous pentoxides that results in varying binding properties
  • A: ‘bioactive bone boundary’, forms a bond with bone
  • B: silicate glasses, act like type 2
  • C: resorbable glasses that disappear within 10-30 days
  • D: non-practical glasses, too weak for implantation
  • collagenous soft tissues can bind to bioactive silicate glasses in specific tiny region (see triangle graph)
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10
Q

Type 3A Surface Reaction stages

A
  • Stage 1: exchange of alkali ions from implant and hydronium ions from solution
  • Stage 2: silica structure breaks down, dissolves at interface
  • Stage 3: re-polymerization of SiO2 rich layers on inactive glass surfaces
  • Stage 4: amorphous film of calcium phosphate precipitates on the silica-rich layer, followed by crystallization to form carbonated-HA crystals (HCA, Stage 5)
  • ALSO: released silica and calcium ions stimulate bone cells to produce more (osteogenic)
  • HA materials can be integrated directly into endogenous (natural) HA through bone resorption
  • Stages must be completed rapidly to properly repair bones, prevents foreign body response (if too fast or slow, might fall into wrong region)
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11
Q

Type 4 Bioceramics

A
  • resorbable, designed to degrade over time and be replaced by bone
  • main crystalline component of bone is calcium-deficient carbonate hydroxyapatite
  • HA and tricalcium phosphate (ceramics) used as fillers, coatings, and cements (helps inspire fusion of mineralized bone)
  • TCP degrades faster, but HA is more osteoconductive
  • challenge to meet proper strength and performance requirements while material degrades, and match resorption rates to ingrowth of natural host tissue
  • various ways of biodegradation
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12
Q

Alumina

A
  • inert bioceramic, extracted from bauxite and cryolite ores
  • dissolved in sodium hydroxide, then precipitated via adding salt
  • finally, uses calcination to form alumina
  • inert, resistant to corrosion, elicits minimal FBR, stable, but very brittle (great hardness and scratch resistance, low coefficient of friction, but not ductile)
  • alloyed with zirconia and chromium oxide (other materials too) to extend implant life
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13
Q

Zirconia

A
  • inert bioceramic
  • extracted from baddeleyite (zirconium oxide mineral)
  • volume changes occur in structural transformations upon cooling when in its pure oxide form (leads to cracking)
  • add yttria or magnesia to stabilize either structure
  • when cracks form in these composites, compressive stress forms to resist the crack front (increased toughness)
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14
Q

Hydroxyapatite

A
  • formed/taken from hydroxylapatite, which mimics mineralized bone
  • bone apatite is deficient in hydroxide (hexagonal crystal structure with lattice vacancies that can be filled)
  • calcium substitution by lead, sodium, etc. destabilizes structure and increases the solubility (can also enhance bone growth culture)
  • widely used as synthetic bone graft substitutes, designed to be osteoinductive (more so osteoconductive)
  • prepared through sintering, heating while pressing
  • make a compromise between mechanical strength and osteoconductivity
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15
Q

Carbon Biomaterials

A
  • inherently biocompatible, with diversity in structure and properties
  • graphite (soft, anisotropic layered in-plane covalent bons, interplane van der Waals interactions) is lubricating
  • diamond (hardest material known, tetrahedral symmetry in three dimensions)
  • spectrum from amorphous to perfect crystalline graphite
  • diverse uses: conjugation of bioactive or fluorescent molecules, like drug delivery, phototherapy and imaging, biosensors, antimicrobial therapy, blood compatible coatings
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16
Q

Pyrolytic Carbon (PyC)

A
  • outstanding blood compatibility properties
  • resists thrombus formation while also having necessary structural properties for long-term usage like in heart valves
  • fluidized bed reactor
  • pyrolytic decomposition (pyrolysis of hydrocarbons in absence of oxygen)
  • small size, lattice imperfections, order within layers not BETWEEN layers (kinked), inter-layer slip is inhibited
  • high flexure strength, low density (can move to accommodate blood flow), similar Young’s modulus to bone, brittle but with good wear resistance, requires hard materials for manufacturing
  • mechanical valve usage, as well as small orthopedic joint replacement