Course: BME 296
Completed discussions on:
Bonding
Structure: cubic cell structure, Miller indices
Defects: 0D, 1D, 2D, 3D and their effects on biomaterial properties
Engage in discussions about common properties encountered in materials.
Composed of two or more elements.
Can have ionic and/or covalent bonds.
Characterized by having more ions than atoms.
Cations (positively charged ions) and anions (negatively charged ions) must be adjacent for stability.
Critical for maximizing the number of nearest neighbors that are anions.
Understand the sizes of cations and anions and the reasons for size disparities.
Affected by two parameters:
Magnitude of the electrical charge on constituent ions.
Physical size of ions (must maintain Rc/Ra < 1 for stability).
Example: CaF2 consists of Ca2+ and 2 F- ions.
Composed of equal numbers of cations and anions with the same charge.
Stable crystal structure example: Sodium Chloride (NaCl).
Compounds where cations and anions have unequal charges (AmXp, where m and/or p≠1).
Example: Zirconia (ZrO2)
Ceramics may also include multiple types of cations (AmBnXp).
Example: Calcium Zirconium silicate: enhances properties for biomedical applications and has apatite forming capability.
Types of point defects: interstitial and vacancy defects in cations and anions.
Importance of maintaining electroneutrality: no individual point defects should occur; group defects sustain neutrality.
Examples of group defects: Schottky defect and Frenkel defect.
Schottky defect: Vacancies in cations and anions in ratios that maintain charge neutrality.
Frenkel defect: Occurs when a cation displacement creates a vacancy, thus maintaining electroneutrality (only applicable for cations).
Metals: metallic bonds, arrangements, and properties relevant to orthopedic implants.
Ceramics: focus on ionic bonds and electroneutrality, explaining their brittleness and applications in dentistry and orthopedic coatings.
Polymers consist of long chains of monomers.
Degree of polymerization signifies number of repeating units.
Molecular weight is critical for understanding polymer characteristics.
Example: Calculate molecular weight of poly tetrafluoroethylene (Teflon) ((C2F4)n).
Atomic mass of C: 12 g/mole; F: 19 g/mole.
Calculation: (2(12)+4(19)=100) g/mole per repeat unit.
For a chain of 14 repeat units, total molecular weight = (1402) g/mole.
Individual components can lead to varying molecular weights within a polymer sample.
Number-average molecular weight (Mn): based on mole fraction of molecules.
Weight-average molecular weight (Mw): based on weight fraction.
Polydispersity index (PI): Ratio of Mw to Mn, indicating sample heterogeneity.
Tasks include calculating number-average and weight-average molecular weights, determining which average significantly impacts results, and computing the polydispersity index.
Linear structures consist of a backbone made of repeating units.
Pendant groups may attach to main chains, influencing properties.
Hydrocarbons serve as basic polymer examples, while vinyl polymers contain carbon-carbon double bonds.
Course focuses on organic polymers, mainly carbon-based.
Inorganic polymers may include different backbones like silicon or phosphorus.
Carbon-carbon single bonds allow for rotation, creating various configurations (stable under non-crowding).
Folded structures play a crucial role in polymer mechanical properties.
Linear vs branched: branched structures affect density and mechanical properties.
Cross-linking increases molecular weight, impacting viscosity and stability.
Thermoplastics can be molded with heat; thermosets cannot be re-shaped after curing.
Isotactic: side groups on the same side of the chain.
Syndiotactic: alternating side groups.
Atactic: random arrangement of side groups.
Influences mechanical properties and is determined by the order of molecules.
Regular arrangements lead to higher strength, whereas irregularities reduce crystalline stability.
Variations include random, alternating, block, and graft copolymers; each has distinct arrangements and properties.
Involves addition, condensation, and genetic engineering techniques for polymer creation.
Steps: initiation (activating monomers), propagation (joining monomers), and termination.
Involves loss of small molecules, such as water or methanol during synthesis.
Allows for more control over polymer architecture via manipulation of genetic code within host organisms.
Example: Reprogramming bacteria to synthesize polymers.
Determine molecular weights based on provided structures and repeat units for PLGA (poly(lactic-co-glycolic acid)).